Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 26122 |
| ensemblid | ENSG00000135999.12 |
| hgncid | 24543 |
| symbol | EPC2 |
| name | enhancer of polycomb homolog 2 |
| refseq_nuc | NM_015630.4 |
| refseq_prot | NP_056445.3 |
| ensembl_nuc | ENST00000258484.11 |
| ensembl_prot | ENSP00000258484.6 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 148644751 |
| end | 148787569 |
| strand | + |
| ver | v1.2 |
| region | chr2:148644751-148787569 |
| region5000 | chr2:148639751-148792569 |
| regionname0 | EPC2_chr2_148644751_148787569 |
| regionname5000 | EPC2_chr2_148639751_148792569 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 807 | 304 | 81 | 40 | 145 | 6 | 30 | 111 | EPC2_chr2_148639751_148792569 | EPC2 | MSKLS others(802): Show |
chr2 | 148639751 | 148792569 |
| a0002 | 0/0 | 807 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | MSKLS others(802): Show |
chr2 | 148639751 | 148792569 |
| a0003 | 0/0 | 807 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | EPC2_chr2_148639751_148792569 | EPC2 | MSKLS others(802): Show |
chr2 | 148639751 | 148792569 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2421 | 296 | 73 | 40 | 145 | 6 | 30 | EPC2_chr2_148639751_148792569 | EPC2 | ATGAG others(2416): Show |
chr2 | 148639751 | 148792569 | ||
| a0001c0003 | 0/0 | 2421 | 3 | 3 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | ATGAG others(2416): Show |
chr2 | 148639751 | 148792569 | ||
| a0001c0004 | 0/0 | 2421 | 2 | 2 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | ATGAG others(2416): Show |
chr2 | 148639751 | 148792569 | ||
| a0001c0005 | 0/0 | 2421 | 2 | 2 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | ATGAG others(2416): Show |
chr2 | 148639751 | 148792569 | ||
| a0001c0006 | 0/0 | 2421 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | ATGAG others(2416): Show |
chr2 | 148639751 | 148792569 | ||
| a0002c0002 | 0/0 | 2421 | 3 | 3 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | ATGAG others(2416): Show |
chr2 | 148639751 | 148792569 | ||
| a0003c0007 | 0/0 | 2421 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | ATGAG others(2416): Show |
chr2 | 148639751 | 148792569 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 3883 | 193 | 71 | 19 | 80 | 3 | 19 | EPC2_chr2_148639751_148792569 | EPC2 | GGTAA others(3878): Show |
chr2 | 148639751 | 148792569 |
| a0001c0001t0002 | 0/0 | 3884 | 84 | 1 | 17 | 52 | 3 | 11 | EPC2_chr2_148639751_148792569 | EPC2 | GGTAA others(3879): Show |
chr2 | 148639751 | 148792569 |
| a0001c0001t0003 | 0/0 | 3884 | 6 | 0 | 2 | 4 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | GGTAA others(3879): Show |
chr2 | 148639751 | 148792569 |
| a0001c0001t0004 | 0/0 | 3883 | 6 | 0 | 0 | 6 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | GGTAA others(3878): Show |
chr2 | 148639751 | 148792569 |
| a0001c0001t0005 | 0/0 | 3880 | 3 | 0 | 2 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | GGTAA others(3875): Show |
chr2 | 148639751 | 148792569 |
| a0001c0001t0007 | 0/0 | 3883 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | GGTAA others(3878): Show |
chr2 | 148639751 | 148792569 |
| a0001c0001t0008 | 0/0 | 3884 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | GGTAA others(3879): Show |
chr2 | 148639751 | 148792569 |
| a0001c0001t0009 | 0/0 | 3883 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | GGTAA others(3878): Show |
chr2 | 148639751 | 148792569 |
| a0001c0001t0010 | 0/1 | 3884 | 1 | 0 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | GGTAA others(3879): Show |
chr2 | 148639751 | 148792569 |
| a0001c0003t0001 | 0/0 | 3883 | 3 | 3 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | GGTAA others(3878): Show |
chr2 | 148639751 | 148792569 |
| a0001c0004t0001 | 0/0 | 3883 | 2 | 2 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | GGTAA others(3878): Show |
chr2 | 148639751 | 148792569 |
| a0001c0005t0001 | 0/0 | 3883 | 2 | 2 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | GGTAA others(3878): Show |
chr2 | 148639751 | 148792569 |
| a0001c0006t0001 | 0/0 | 3883 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | GGTAA others(3878): Show |
chr2 | 148639751 | 148792569 |
| a0002c0002t0001 | 0/0 | 3883 | 2 | 2 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | GGTAA others(3878): Show |
chr2 | 148639751 | 148792569 |
| a0002c0002t0006 | 0/0 | 3883 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | GGTAA others(3878): Show |
chr2 | 148639751 | 148792569 |
| a0003c0007t0001 | 0/0 | 3883 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | GGTAA others(3878): Show |
chr2 | 148639751 | 148792569 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0018 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0003g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0003g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0004g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0004g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0004g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0004g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0004g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0005g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0005g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0005g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0007g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0008g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0009g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0001t0010g0169 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0003t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0003t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0003t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0004t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0004t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0005t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0005t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0001c0006t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0002c0002t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0002c0002t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0002c0002t0006g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| a0003c0007t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0258 | EUR | FIN | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0066 | EUR | FIN | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | CHS | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0116 | EAS | CHS | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | CHS | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG00544 | hp2 | a0001 | c0001 | t0004 | g0177 | EAS | CHS | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | CHS | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG00558 | hp2 | a0001 | c0001 | t0003 | g0084 | EAS | CHS | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | CHS | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG00609 | hp2 | a0001 | c0001 | t0004 | g0181 | EAS | CHS | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0242 | AMR | PUR | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0188 | AMR | PUR | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0097 | AMR | PUR | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0063 | EAS | CHS | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | CHS | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0070 | AMR | PUR | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0255 | AMR | PUR | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0208 | AMR | PUR | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0045 | AMR | PUR | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0111 | AMR | PUR | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0112 | AMR | PUR | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0046 | AMR | PUR | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0206 | AMR | PUR | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0219 | AMR | PUR | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0037 | AMR | PUR | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0048 | AMR | PUR | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0207 | AMR | PUR | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0057 | AMR | PUR | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0180 | AMR | PUR | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0051 | AMR | PUR | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0225 | AMR | PUR | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | CLM | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0222 | AMR | CLM | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0053 | AMR | CLM | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0161 | AMR | CLM | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0049 | AMR | CLM | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0213 | AMR | CLM | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0205 | AMR | CLM | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0123 | AMR | CLM | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0133 | AMR | CLM | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0201 | AMR | CLM | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0055 | EUR | IBS | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0257 | EUR | IBS | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0228 | EUR | IBS | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0056 | EUR | IBS | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG01884 | hp1 | a0001 | c0003 | t0001 | g0249 | AFR | ACB | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0069 | AFR | ACB | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG01891 | hp1 | a0001 | c0004 | t0001 | g0013 | AFR | ACB | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0245 | AFR | ACB | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0047 | AMR | PEL | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG01943 | hp2 | a0001 | c0001 | t0005 | g0210 | AMR | PEL | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0262 | AMR | PEL | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG01981 | hp2 | a0001 | c0001 | t0003 | g0121 | AMR | PEL | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0204 | AMR | PEL | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG02004 | hp2 | a0001 | c0001 | t0003 | g0094 | AMR | PEL | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | KHV | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0105 | EAS | KHV | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0126 | EAS | KHV | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | KHV | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0095 | EAS | KHV | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | KHV | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | KHV | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0085 | EAS | KHV | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0072 | EAS | KHV | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0298 | EAS | KHV | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | KHV | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0079 | EAS | KHV | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | KHV | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0071 | EAS | KHV | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | KHV | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0119 | EAS | KHV | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | ACB | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | CDX | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0068 | EAS | CDX | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0282 | AFR | ACB | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG02257 | hp2 | a0001 | c0005 | t0001 | g0009 | AFR | ACB | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | ACB | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0059 | AMR | PEL | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG02273 | hp2 | a0001 | c0001 | t0005 | g0221 | AMR | PEL | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG02451 | hp1 | a0001 | c0006 | t0001 | g0007 | AFR | ACB | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0109 | EAS | KHV | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | KHV | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0275 | AFR | GWD | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0252 | AFR | GWD | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0127 | SAS | PJL | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0197 | SAS | PJL | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0276 | AFR | GWD | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0231 | AFR | GWD | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG02622 | hp2 | a0001 | c0003 | t0001 | g0270 | AFR | GWD | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0280 | AFR | GWD | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG02647 | hp2 | a0001 | c0005 | t0001 | g0186 | AFR | GWD | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0248 | AFR | GWD | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0251 | AFR | GWD | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG02723 | hp2 | a0001 | c0001 | t0007 | g0217 | AFR | GWD | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | GWD | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0235 | AFR | GWD | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0279 | AFR | GWD | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0199 | AFR | GWD | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0193 | AFR | GWD | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | GWD | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | GWD | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0277 | AFR | GWD | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0241 | AFR | GWD | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0304 | AFR | ESN | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | ESN | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG02965 | hp1 | a0002 | c0002 | t0001 | g0307 | AFR | ESN | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0250 | AFR | ESN | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | ESN | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | ESN | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | ESN | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0260 | SAS | PJL | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0259 | SAS | PJL | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | GWD | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0224 | AFR | GWD | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0195 | AFR | MSL | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | MSL | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | ESN | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0226 | AFR | ESN | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0274 | AFR | ESN | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | ESN | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | ESN | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0281 | AFR | MSL | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0267 | AFR | MSL | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0243 | AFR | MSL | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0306 | AFR | MSL | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0244 | AFR | MSL | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | MSL | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | MSL | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | MSL | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0122 | SAS | PJL | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0237 | SAS | PJL | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0170 | SAS | PJL | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0179 | SAS | PJL | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0174 | SAS | PJL | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0236 | SAS | PJL | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | ESN | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | MSL | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0278 | AFR | MSL | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0261 | SAS | PJL | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0092 | SAS | PJL | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0230 | SAS | PJL | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0060 | SAS | PJL | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0273 | SAS | PJL | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0038 | SAS | PJL | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0215 | SAS | PJL | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0178 | SAS | PJL | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0233 | SAS | BEB | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0067 | SAS | BEB | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0139 | SAS | BEB | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0054 | SAS | BEB | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0061 | SAS | BEB | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | BEB | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0093 | SAS | BEB | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0246 | SAS | BEB | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0256 | SAS | STU | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0052 | SAS | STU | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0110 | EAS | CHB | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | CHB | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | CHB | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0086 | EAS | CHB | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| NA18939 | hp1 | a0001 | c0001 | t0008 | g0039 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| NA18945 | hp1 | a0001 | c0001 | t0003 | g0074 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0101 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| NA18956 | hp2 | a0001 | c0001 | t0002 | g0117 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| NA18959 | hp1 | a0001 | c0001 | t0003 | g0108 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| NA18963 | hp1 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| NA18968 | hp1 | a0001 | c0001 | t0003 | g0062 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0107 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0114 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| NA18971 | hp2 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0128 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| NA18985 | hp1 | a0001 | c0001 | t0002 | g0113 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| NA18990 | hp1 | a0001 | c0001 | t0004 | g0176 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0118 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| NA19004 | hp1 | a0001 | c0001 | t0004 | g0173 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0268 | AFR | LWK | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| NA19030 | hp2 | a0001 | c0004 | t0001 | g0026 | AFR | LWK | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0271 | AFR | LWK | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0192 | AFR | LWK | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| NA19056 | hp2 | a0001 | c0001 | t0009 | g0296 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0124 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0099 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| NA19065 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| NA19070 | hp2 | a0001 | c0001 | t0005 | g0011 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| NA19083 | hp1 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| NA19086 | hp2 | a0003 | c0007 | t0001 | g0138 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0120 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | YRI | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0239 | AFR | YRI | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | ASW | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | ASW | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0073 | SAS | GIH | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0175 | SAS | GIH | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | CLM | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0050 | AMR | CLM | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG02109 | hp1 | a0001 | c0003 | t0001 | g0269 | AFR | ACB | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0240 | AFR | ACB | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0272 | AFR | MSL | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0229 | AFR | MSL | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | USA | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0234 | AFR | USA | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| NA20300 | hp1 | a0002 | c0002 | t0006 | g0254 | AFR | USA | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | USA | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| NA21309 | hp1 | a0002 | c0002 | t0001 | g0253 | AFR | LWK | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0305 | AFR | LWK | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0010 | g0169 | REF | REF | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0018 | REF | REF | EPC2_chr2_148639751_148792569 | EPC2 | chr2 | 148639751 | 148792569 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:148762780 | A | G | 1 | a0003 | 1 | NA19086.hp2 | missense_variant | MODERATE | c.926A>G | p.Lys309Arg | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 6/14 | 1193/3883 | 926/2424 | 309/807 | chr2 | 148762780 | |||
| chr2:148771169 | A | G | 1 | a0002 | 3 | HG02965.hp1 NA20300.hp1 NA21309.hp1 |
missense_variant | MODERATE | c.1502A>G | p.Asn501Ser | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/14 | 1769/3883 | 1502/2424 | 501/807 | chr2 | 148771169 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:148645035 | C | T | 1 | a0001c0003 | 3 | HG01884.hp1 HG02109.hp1 HG02622.hp2 |
synonymous_variant | LOW | c.18C>T | p.Phe6Phe | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/14 | 285/3883 | 18/2424 | 6/807 | chr2 | 148645035 | |||
| chr2:148761868 | T | A | 1 | a0001c0006 | 1 | HG02451.hp1 | synonymous_variant | LOW | c.753T>A | p.Ile251Ile | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 5/14 | 1020/3883 | 753/2424 | 251/807 | chr2 | 148761868 | |||
| chr2:148761874 | A | G | 1 | a0001c0005 | 2 | HG02257.hp2 HG02647.hp2 |
synonymous_variant | LOW | c.759A>G | p.Arg253Arg | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 5/14 | 1026/3883 | 759/2424 | 253/807 | chr2 | 148761874 | |||
| chr2:148781756 | G | A | 1 | a0001c0004 | 2 | HG01891.hp1 NA19030.hp2 |
synonymous_variant | LOW | c.1833G>A | p.Ser611Ser | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 11/14 | 2100/3883 | 1833/2424 | 611/807 | chr2 | 148781756 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:148786476 | A | G | 1 | a0001c0001t0009 | 1 | NA19056.hp2 | 3_prime_UTR_variant | MODIFIER | c.*99A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 14/14 | 99 | chr2 | 148786476 | ||||||
| chr2:148786517 | T | C | 1 | a0001c0001t0003 | 6 | HG00558.hp2 HG01981.hp2 HG02004.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*140T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 14/14 | 140 | chr2 | 148786517 | ||||||
| chr2:148786993 | C | A | 1 | a0001c0001t0004 | 6 | HG00544.hp2 HG00609.hp2 NA18971.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*616C>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 14/14 | 616 | chr2 | 148786993 | ||||||
| chr2:148787031 | A | G | 1 | a0001c0001t0008 | 1 | NA18939.hp1 | 3_prime_UTR_variant | MODIFIER | c.*654A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 14/14 | 654 | chr2 | 148787031 | ||||||
| chr2:148787062 | TAAA | T | 1 | a0001c0001t0005 | 3 | HG01943.hp2 HG02273.hp2 NA19070.hp2 |
3_prime_UTR_variant | MODIFIER | c.*689_*691delAAA | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 14/14 | 689 | INFO_REALIGN_3_PRIME | chr2 | 148787062 | |||||
| chr2:148787079 | G | GA | 3 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0008 |
91 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(88): Show |
3_prime_UTR_variant | MODIFIER | c.*708dupA | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 14/14 | 709 | INFO_REALIGN_3_PRIME | chr2 | 148787079 | |||||
| chr2:148787170 | G | A | 1 | a0002c0002t0006 | 1 | NA20300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*793G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 14/14 | 793 | chr2 | 148787170 | ||||||
| chr2:148787337 | A | C | 1 | a0001c0001t0007 | 1 | HG02723.hp2 | 3_prime_UTR_variant | MODIFIER | c.*960A>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 14/14 | 960 | chr2 | 148787337 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:148645492 | C | T | 1 | a0002c0002t0001g0307 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.153+322C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148645492 | |||||||
| chr2:148645516 | C | T | 1 | a0001c0001t0001g0306 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.153+346C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148645516 | |||||||
| chr2:148645644 | C | T | 1 | a0001c0001t0001g0305 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.153+474C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148645644 | |||||||
| chr2:148645809 | G | A | 1 | a0001c0001t0001g0002 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.153+639G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148645809 | |||||||
| chr2:148645817 | G | A | 4 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(1): Show |
4 | HG02145.hp1 HG02451.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.153+647G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148645817 | |||||||
| chr2:148645826 | G | A | 4 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(1): Show |
4 | HG02145.hp1 HG02451.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.153+656G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148645826 | |||||||
| chr2:148645826 | G | C | 1 | a0001c0006t0001g0007 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.153+656G>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148645826 | |||||||
| chr2:148645827 | C | T | 4 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(1): Show |
4 | HG02145.hp1 HG02451.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.153+657C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148645827 | |||||||
| chr2:148645842 | C | T | 1 | a0001c0001t0001g0304 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.153+672C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148645842 | |||||||
| chr2:148646051 | G | A | 1 | a0001c0001t0001g0008 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.153+881G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148646051 | |||||||
| chr2:148646238 | G | A | 1 | a0001c0005t0001g0009 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.153+1068G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148646238 | |||||||
| chr2:148646470 | AATAG | A | 15 | a0001c0001t0001g0289 a0001c0001t0001g0290 a0001c0001t0001g0291 others(12): Show |
15 | HG00673.hp2 HG02074.hp2 NA18949.hp2 others(12): Show |
intron_variant | MODIFIER | c.153+1304_153+1307d others(6): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148646470 | ||||||
| chr2:148646493 | A | G | 6 | a0001c0001t0001g0283 a0001c0001t0001g0284 a0001c0001t0001g0285 others(3): Show |
6 | NA18747.hp1 NA18947.hp2 NA18952.hp1 others(3): Show |
intron_variant | MODIFIER | c.153+1323A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148646493 | |||||||
| chr2:148646601 | C | CT | 286 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(283): Show |
287 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(284): Show |
intron_variant | MODIFIER | c.153+1441dupT | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148646601 | ||||||
| chr2:148646917 | C | T | 10 | a0001c0001t0001g0274 a0001c0001t0001g0275 a0001c0001t0001g0276 others(7): Show |
10 | HG02257.hp1 HG02257.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.153+1747C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148646917 | |||||||
| chr2:148646924 | G | A | 108 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(105): Show |
108 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(105): Show |
intron_variant | MODIFIER | c.153+1754G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148646924 | |||||||
| chr2:148646955 | C | T | 98 | a0001c0001t0001g0036 a0001c0001t0001g0042 a0001c0001t0001g0043 others(95): Show |
98 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(95): Show |
intron_variant | MODIFIER | c.153+1785C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148646955 | |||||||
| chr2:148646982 | C | T | 1 | a0001c0001t0002g0133 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.153+1812C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148646982 | |||||||
| chr2:148647002 | C | T | 2 | a0001c0001t0001g0281 a0001c0001t0001g0282 |
2 | HG02257.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.153+1832C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148647002 | |||||||
| chr2:148647387 | A | G | 1 | a0001c0001t0001g0304 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.153+2217A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148647387 | |||||||
| chr2:148647496 | C | T | 1 | a0001c0001t0001g0303 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.153+2326C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148647496 | |||||||
| chr2:148647609 | G | A | 41 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0136 others(38): Show |
41 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.153+2439G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148647609 | |||||||
| chr2:148647619 | C | CT | 7 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0131 others(4): Show |
7 | HG02647.hp1 HG02809.hp1 HG03486.hp2 others(4): Show |
intron_variant | MODIFIER | c.153+2476dupT | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148647619 | ||||||
| chr2:148647619 | CT | C | 106 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0135 others(103): Show |
106 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(103): Show |
intron_variant | MODIFIER | c.153+2476delT | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148647619 | ||||||
| chr2:148647619 | CTT | C | 43 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(40): Show |
44 | HG00544.hp2 HG00609.hp2 HG00673.hp2 others(41): Show |
intron_variant | MODIFIER | c.153+2475_153+2476d others(4): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148647619 | ||||||
| chr2:148647619 | CTTT | C | 81 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0290 others(78): Show |
81 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(78): Show |
intron_variant | MODIFIER | c.153+2474_153+2476d others(5): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148647619 | ||||||
| chr2:148647619 | CTTTT | C | 6 | a0001c0001t0001g0036 a0001c0001t0002g0037 a0001c0001t0002g0038 others(3): Show |
6 | HG01070.hp2 HG02895.hp1 HG03704.hp2 others(3): Show |
intron_variant | MODIFIER | c.153+2473_153+2476d others(6): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148647619 | ||||||
| chr2:148647619 | CTTTTTT | C | 8 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(5): Show |
8 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(5): Show |
intron_variant | MODIFIER | c.153+2471_153+2476d others(8): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148647619 | ||||||
| chr2:148647646 | T | A | 1 | a0001c0005t0001g0186 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.153+2476T>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148647646 | |||||||
| chr2:148647661 | T | C | 4 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(1): Show |
4 | HG00639.hp2 HG02809.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.153+2491T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148647661 | |||||||
| chr2:148647709 | T | G | 5 | a0001c0001t0001g0274 a0001c0001t0001g0275 a0001c0001t0001g0276 others(2): Show |
5 | HG02572.hp1 HG02615.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.153+2539T>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148647709 | |||||||
| chr2:148647910 | G | A | 1 | a0001c0001t0001g0187 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.153+2740G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148647910 | |||||||
| chr2:148647976 | A | G | 1 | a0001c0001t0001g0301 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.153+2806A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148647976 | |||||||
| chr2:148648025 | A | C | 1 | a0001c0001t0002g0120 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.153+2855A>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148648025 | |||||||
| chr2:148648071 | A | G | 20 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0001g0184 others(17): Show |
20 | HG00673.hp2 HG02074.hp2 HG04204.hp1 others(17): Show |
intron_variant | MODIFIER | c.153+2901A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148648071 | |||||||
| chr2:148648072 | G | A | 1 | a0001c0001t0001g0188 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.153+2902G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148648072 | |||||||
| chr2:148648234 | TTTTCTTT others(3): Show |
T | 1 | a0001c0001t0001g0255 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.153+3074_153+3083d others(12): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148648234 | ||||||
| chr2:148648275 | T | C | 5 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0191 others(2): Show |
5 | HG02258.hp1 HG02886.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.153+3105T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148648275 | |||||||
| chr2:148648288 | A | C | 35 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0178 others(32): Show |
36 | HG00544.hp2 HG00609.hp2 HG00673.hp2 others(33): Show |
intron_variant | MODIFIER | c.153+3118A>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148648288 | |||||||
| chr2:148648528 | A | C | 11 | a0001c0001t0001g0028 a0001c0001t0001g0274 a0001c0001t0001g0275 others(8): Show |
11 | HG02257.hp1 HG02257.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.153+3358A>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148648528 | |||||||
| chr2:148648555 | A | G | 1 | a0001c0006t0001g0007 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.153+3385A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148648555 | |||||||
| chr2:148648822 | T | G | 3 | a0001c0001t0001g0036 a0001c0001t0001g0042 a0001c0001t0001g0043 |
3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.153+3652T>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148648822 | |||||||
| chr2:148648860 | C | A | 91 | a0001c0001t0002g0037 a0001c0001t0002g0038 a0001c0001t0002g0040 others(88): Show |
91 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.153+3690C>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148648860 | |||||||
| chr2:148649061 | G | A | 108 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(105): Show |
108 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(105): Show |
intron_variant | MODIFIER | c.153+3891G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148649061 | |||||||
| chr2:148649072 | A | C | 1 | a0001c0001t0001g0167 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.153+3902A>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148649072 | |||||||
| chr2:148649133 | T | C | 1 | a0001c0001t0001g0304 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.153+3963T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148649133 | |||||||
| chr2:148649311 | T | C | 3 | a0001c0001t0001g0036 a0001c0001t0001g0042 a0001c0001t0001g0043 |
3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.153+4141T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148649311 | |||||||
| chr2:148649394 | G | A | 1 | a0001c0001t0002g0044 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.153+4224G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148649394 | |||||||
| chr2:148649472 | G | A | 4 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(1): Show |
4 | HG00639.hp2 HG02809.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.153+4302G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148649472 | |||||||
| chr2:148649746 | T | A | 1 | a0001c0001t0001g0194 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.153+4576T>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148649746 | |||||||
| chr2:148650089 | C | T | 1 | a0001c0001t0001g0166 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.153+4919C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148650089 | |||||||
| chr2:148650181 | T | C | 8 | a0001c0001t0002g0037 a0001c0001t0002g0045 a0001c0001t0002g0046 others(5): Show |
8 | HG00738.hp2 HG01069.hp1 HG01070.hp2 others(5): Show |
intron_variant | MODIFIER | c.153+5011T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148650181 | |||||||
| chr2:148650368 | T | C | 1 | a0001c0001t0002g0052 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.153+5198T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148650368 | |||||||
| chr2:148650382 | A | G | 2 | a0001c0001t0001g0158 a0001c0001t0001g0159 |
2 | NA18969.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.153+5212A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148650382 | |||||||
| chr2:148650670 | A | G | 164 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(161): Show |
165 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(162): Show |
intron_variant | MODIFIER | c.153+5500A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148650670 | |||||||
| chr2:148650748 | G | A | 1 | a0001c0001t0001g0195 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.153+5578G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148650748 | |||||||
| chr2:148650766 | G | GT | 103 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0178 others(100): Show |
104 | HG00280.hp2 HG00423.hp2 HG00544.hp2 others(101): Show |
intron_variant | MODIFIER | c.153+5597dupT | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148650766 | ||||||
| chr2:148650899 | A | G | 5 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0001c0003t0001g0249 others(2): Show |
5 | HG01884.hp1 HG02109.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.153+5729A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148650899 | |||||||
| chr2:148651263 | C | G | 3 | a0001c0001t0001g0250 a0001c0001t0001g0251 a0001c0001t0001g0252 |
3 | HG02572.hp2 HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.153+6093C>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148651263 | |||||||
| chr2:148651355 | G | A | 95 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(92): Show |
95 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.153+6185G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148651355 | |||||||
| chr2:148651392 | C | G | 4 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(1): Show |
4 | HG00639.hp2 HG02809.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.153+6222C>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148651392 | |||||||
| chr2:148651466 | G | C | 1 | a0001c0001t0002g0044 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.153+6296G>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148651466 | |||||||
| chr2:148651552 | C | G | 3 | a0001c0001t0001g0036 a0001c0001t0001g0042 a0001c0001t0001g0043 |
3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.153+6382C>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148651552 | |||||||
| chr2:148651553 | T | A | 1 | a0001c0001t0001g0196 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.153+6383T>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148651553 | |||||||
| chr2:148651555 | G | A | 1 | a0001c0001t0001g0196 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.153+6385G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148651555 | |||||||
| chr2:148651561 | T | G | 1 | a0001c0001t0001g0196 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.153+6391T>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148651561 | |||||||
| chr2:148651562 | G | C | 1 | a0001c0001t0001g0196 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.153+6392G>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148651562 | |||||||
| chr2:148651564 | A | G | 1 | a0001c0001t0001g0196 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.153+6394A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148651564 | |||||||
| chr2:148651565 | GGGT | G | 10 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(7): Show |
10 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(7): Show |
intron_variant | MODIFIER | c.153+6399_153+6401d others(5): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148651565 | ||||||
| chr2:148651567 | G | A | 1 | a0001c0001t0001g0196 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.153+6397G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148651567 | |||||||
| chr2:148651569 | G | T | 1 | a0001c0001t0001g0196 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.153+6399G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148651569 | |||||||
| chr2:148651573 | T | A | 1 | a0001c0001t0001g0196 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.153+6403T>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148651573 | |||||||
| chr2:148651574 | A | G | 1 | a0001c0001t0001g0196 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.153+6404A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148651574 | |||||||
| chr2:148651575 | G | C | 1 | a0001c0001t0001g0196 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.153+6405G>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148651575 | |||||||
| chr2:148651583 | A | G | 1 | a0001c0001t0001g0196 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.153+6413A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148651583 | |||||||
| chr2:148651590 | A | C | 1 | a0001c0001t0001g0196 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.153+6420A>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148651590 | |||||||
| chr2:148651593 | T | C | 1 | a0001c0001t0001g0196 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.153+6423T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148651593 | |||||||
| chr2:148651594 | A | C | 1 | a0001c0001t0001g0196 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.153+6424A>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148651594 | |||||||
| chr2:148651596 | G | A | 1 | a0001c0001t0001g0196 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.153+6426G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148651596 | |||||||
| chr2:148651598 | T | G | 1 | a0001c0001t0001g0196 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.153+6428T>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148651598 | |||||||
| chr2:148651599 | T | G | 1 | a0001c0001t0001g0196 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.153+6429T>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148651599 | |||||||
| chr2:148651600 | C | A | 1 | a0001c0001t0001g0196 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.153+6430C>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148651600 | |||||||
| chr2:148651602 | G | A | 1 | a0001c0001t0001g0196 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.153+6432G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148651602 | |||||||
| chr2:148651611 | G | T | 1 | a0001c0001t0001g0196 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.153+6441G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148651611 | |||||||
| chr2:148651615 | C | T | 1 | a0001c0001t0001g0196 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.153+6445C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148651615 | |||||||
| chr2:148651618 | G | A | 1 | a0001c0001t0001g0196 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.153+6448G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148651618 | |||||||
| chr2:148651619 | T | A | 1 | a0001c0001t0001g0196 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.153+6449T>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148651619 | |||||||
| chr2:148651623 | G | T | 1 | a0001c0001t0001g0196 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.153+6453G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148651623 | |||||||
| chr2:148651624 | G | A | 1 | a0001c0001t0001g0196 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.153+6454G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148651624 | |||||||
| chr2:148651625 | T | C | 1 | a0001c0001t0001g0196 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.153+6455T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148651625 | |||||||
| chr2:148651629 | C | T | 1 | a0001c0001t0001g0196 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.153+6459C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148651629 | |||||||
| chr2:148651631 | T | A | 1 | a0001c0001t0001g0196 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.153+6461T>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148651631 | |||||||
| chr2:148651632 | G | A | 1 | a0001c0001t0001g0196 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.153+6462G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148651632 | |||||||
| chr2:148651633 | G | T | 1 | a0001c0001t0001g0196 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.153+6463G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148651633 | |||||||
| chr2:148651634 | A | T | 1 | a0001c0001t0001g0196 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.153+6464A>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148651634 | |||||||
| chr2:148651637 | A | C | 1 | a0001c0001t0001g0196 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.153+6467A>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148651637 | |||||||
| chr2:148651639 | C | A | 1 | a0001c0001t0001g0196 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.153+6469C>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148651639 | |||||||
| chr2:148651640 | C | G | 1 | a0001c0001t0001g0196 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.153+6470C>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148651640 | |||||||
| chr2:148651644 | T | A | 1 | a0001c0001t0001g0196 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.153+6474T>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148651644 | |||||||
| chr2:148651650 | C | A | 1 | a0001c0001t0001g0196 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.153+6480C>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148651650 | |||||||
| chr2:148651651 | T | A | 1 | a0001c0001t0001g0196 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.153+6481T>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148651651 | |||||||
| chr2:148651656 | G | T | 1 | a0001c0001t0001g0196 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.153+6486G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148651656 | |||||||
| chr2:148651657 | G | C | 1 | a0001c0001t0001g0196 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.153+6487G>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148651657 | |||||||
| chr2:148651658 | G | C | 1 | a0001c0001t0001g0196 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.153+6488G>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148651658 | |||||||
| chr2:148651662 | A | T | 1 | a0001c0001t0001g0196 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.153+6492A>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148651662 | |||||||
| chr2:148651666 | G | C | 1 | a0001c0001t0001g0196 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.153+6496G>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148651666 | |||||||
| chr2:148651671 | A | T | 1 | a0001c0001t0001g0196 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.153+6501A>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148651671 | |||||||
| chr2:148651680 | A | T | 1 | a0001c0001t0001g0196 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.153+6510A>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148651680 | |||||||
| chr2:148651681 | A | T | 1 | a0001c0001t0001g0196 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.153+6511A>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148651681 | |||||||
| chr2:148651682 | G | T | 1 | a0001c0001t0001g0196 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.153+6512G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148651682 | |||||||
| chr2:148651686 | C | A | 1 | a0001c0001t0001g0196 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.153+6516C>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148651686 | |||||||
| chr2:148651744 | T | C | 1 | a0001c0001t0001g0197 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.153+6574T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148651744 | |||||||
| chr2:148651772 | A | G | 4 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(1): Show |
4 | HG00639.hp2 HG02809.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.153+6602A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148651772 | |||||||
| chr2:148651842 | T | A | 91 | a0001c0001t0002g0037 a0001c0001t0002g0038 a0001c0001t0002g0040 others(88): Show |
91 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.153+6672T>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148651842 | |||||||
| chr2:148651876 | T | C | 9 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(6): Show |
9 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.153+6706T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148651876 | |||||||
| chr2:148651886 | C | T | 5 | a0001c0001t0002g0115 a0001c0001t0002g0116 a0001c0001t0002g0117 others(2): Show |
5 | HG00423.hp2 HG02135.hp2 NA18956.hp2 others(2): Show |
intron_variant | MODIFIER | c.153+6716C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148651886 | |||||||
| chr2:148651901 | G | A | 2 | a0001c0001t0001g0198 a0001c0001t0001g0199 |
2 | HG02818.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.153+6731G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148651901 | |||||||
| chr2:148651936 | C | G | 1 | a0001c0001t0001g0268 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.153+6766C>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148651936 | |||||||
| chr2:148652070 | G | A | 5 | a0001c0001t0002g0053 a0001c0001t0002g0054 a0001c0001t0002g0055 others(2): Show |
5 | HG01106.hp1 HG01258.hp1 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.153+6900G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148652070 | |||||||
| chr2:148652499 | G | A | 95 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(92): Show |
95 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.153+7329G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148652499 | |||||||
| chr2:148652506 | C | T | 1 | a0001c0001t0002g0114 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.153+7336C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148652506 | |||||||
| chr2:148652542 | T | A | 1 | a0001c0001t0001g0158 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.153+7372T>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148652542 | |||||||
| chr2:148652572 | T | C | 1 | a0001c0001t0001g0291 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.153+7402T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148652572 | |||||||
| chr2:148652621 | C | T | 95 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(92): Show |
95 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.153+7451C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148652621 | |||||||
| chr2:148652664 | TGAAAA | T | 9 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(6): Show |
9 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.153+7498_153+7502d others(7): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148652664 | ||||||
| chr2:148652757 | C | T | 1 | a0001c0001t0001g0248 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.153+7587C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148652757 | |||||||
| chr2:148652773 | G | A | 1 | a0002c0002t0001g0253 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.153+7603G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148652773 | |||||||
| chr2:148653087 | A | G | 1 | a0001c0001t0001g0267 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.153+7917A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148653087 | |||||||
| chr2:148653350 | A | G | 2 | a0001c0001t0001g0251 a0001c0001t0001g0252 |
2 | HG02572.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.153+8180A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148653350 | |||||||
| chr2:148653363 | C | A | 108 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(105): Show |
108 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(105): Show |
intron_variant | MODIFIER | c.153+8193C>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148653363 | |||||||
| chr2:148653363 | C | T | 4 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(1): Show |
4 | HG02145.hp1 HG02451.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.153+8193C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148653363 | |||||||
| chr2:148653583 | T | G | 290 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(287): Show |
291 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(288): Show |
intron_variant | MODIFIER | c.153+8413T>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148653583 | |||||||
| chr2:148653681 | A | G | 1 | a0002c0002t0001g0253 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.153+8511A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148653681 | |||||||
| chr2:148653791 | TGAA | T | 91 | a0001c0001t0002g0037 a0001c0001t0002g0038 a0001c0001t0002g0040 others(88): Show |
91 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.153+8623_153+8625d others(5): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148653791 | ||||||
| chr2:148653950 | G | GT | 12 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(9): Show |
12 | HG02071.hp1 HG02135.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.153+8794dupT | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148653950 | ||||||
| chr2:148653950 | GT | G | 101 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(98): Show |
101 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(98): Show |
intron_variant | MODIFIER | c.153+8794delT | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148653950 | ||||||
| chr2:148653990 | C | A | 1 | a0001c0001t0003g0121 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.153+8820C>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148653990 | |||||||
| chr2:148654004 | A | G | 9 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(6): Show |
9 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.153+8834A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148654004 | |||||||
| chr2:148654030 | C | T | 1 | a0001c0001t0002g0110 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.153+8860C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148654030 | |||||||
| chr2:148654105 | C | T | 1 | a0001c0001t0001g0301 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.153+8935C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148654105 | |||||||
| chr2:148654325 | T | C | 6 | a0001c0001t0001g0274 a0001c0001t0001g0275 a0001c0001t0001g0276 others(3): Show |
6 | HG02572.hp1 HG02615.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.153+9155T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148654325 | |||||||
| chr2:148654642 | A | T | 1 | a0001c0001t0001g0246 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.153+9472A>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148654642 | |||||||
| chr2:148654731 | C | A | 95 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(92): Show |
95 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.153+9561C>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148654731 | |||||||
| chr2:148654787 | G | C | 1 | a0001c0001t0001g0002 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.153+9617G>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148654787 | |||||||
| chr2:148654832 | C | T | 8 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(5): Show |
8 | HG01884.hp1 HG02040.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.153+9662C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148654832 | |||||||
| chr2:148654998 | G | C | 1 | a0001c0001t0001g0160 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.153+9828G>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148654998 | |||||||
| chr2:148655188 | C | G | 1 | a0001c0001t0001g0032 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.153+10018C>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148655188 | |||||||
| chr2:148655508 | T | C | 91 | a0001c0001t0002g0037 a0001c0001t0002g0038 a0001c0001t0002g0040 others(88): Show |
91 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.153+10338T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148655508 | |||||||
| chr2:148655906 | T | G | 10 | a0001c0001t0001g0274 a0001c0001t0001g0275 a0001c0001t0001g0276 others(7): Show |
10 | HG02257.hp1 HG02257.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.153+10736T>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148655906 | |||||||
| chr2:148655960 | C | T | 3 | a0001c0001t0001g0036 a0001c0001t0001g0042 a0001c0001t0001g0043 |
3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.153+10790C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148655960 | |||||||
| chr2:148656001 | C | CTGTGTGT others(1): Show |
7 | a0001c0001t0002g0059 a0001c0001t0002g0061 a0001c0001t0002g0115 others(4): Show |
7 | HG00423.hp2 HG02273.hp1 HG03942.hp1 others(4): Show |
intron_variant | MODIFIER | c.153+10848_153+1085 others(12): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148656001 | ||||||
| chr2:148656001 | C | CTGTGTGT others(3): Show |
53 | a0001c0001t0002g0038 a0001c0001t0002g0041 a0001c0001t0002g0044 others(50): Show |
53 | HG00280.hp2 HG00558.hp2 HG00642.hp2 others(50): Show |
intron_variant | MODIFIER | c.153+10846_153+1085 others(14): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148656001 | ||||||
| chr2:148656001 | C | CTGTGTGT others(5): Show |
24 | a0001c0001t0002g0037 a0001c0001t0002g0040 a0001c0001t0002g0045 others(21): Show |
24 | HG00738.hp2 HG01069.hp1 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.153+10844_153+1085 others(16): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148656001 | ||||||
| chr2:148656001 | C | CTGTGTGT others(7): Show |
1 | a0001c0001t0002g0057 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.153+10842_153+1085 others(18): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148656001 | ||||||
| chr2:148656001 | C | CTGTGTGT others(9): Show |
3 | a0001c0001t0002g0106 a0001c0001t0002g0107 a0001c0001t0003g0108 |
3 | NA18959.hp1 NA18969.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.153+10840_153+1085 others(20): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148656001 | ||||||
| chr2:148656001 | C | CTGTGTGT others(11): Show |
1 | a0001c0001t0002g0109 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.153+10838_153+1085 others(22): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148656001 | ||||||
| chr2:148656001 | C | CTGTGTT | 11 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(8): Show |
11 | HG00639.hp2 HG02040.hp2 HG02132.hp1 others(8): Show |
intron_variant | MODIFIER | c.153+10836_153+1083 others(10): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148656001 | ||||||
| chr2:148656001 | C | CTGTGTTT others(1): Show |
7 | a0001c0001t0001g0031 a0001c0001t0001g0276 a0001c0001t0001g0277 others(4): Show |
7 | HG02257.hp2 HG02615.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.153+10836_153+1083 others(12): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148656001 | ||||||
| chr2:148656001 | C | CTGTGTTT others(15): Show |
1 | a0001c0001t0001g0304 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.153+10836_153+1083 others(26): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148656001 | ||||||
| chr2:148656003 | G | GTGTT | 15 | a0001c0001t0001g0036 a0001c0001t0001g0042 a0001c0001t0001g0043 others(12): Show |
15 | HG00639.hp1 HG00642.hp1 HG01517.hp1 others(12): Show |
intron_variant | MODIFIER | c.153+10836_153+1083 others(8): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148656003 | ||||||
| chr2:148656005 | G | GTT | 57 | a0001c0001t0001g0008 a0001c0001t0001g0028 a0001c0001t0001g0134 others(54): Show |
57 | HG00544.hp2 HG00558.hp1 HG00609.hp1 others(54): Show |
intron_variant | MODIFIER | c.153+10836_153+1083 others(6): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148656005 | ||||||
| chr2:148656007 | G | T | 108 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(105): Show |
109 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(106): Show |
intron_variant | MODIFIER | c.153+10837G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148656007 | |||||||
| chr2:148656022 | T | G | 1 | a0001c0005t0001g0186 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.153+10852T>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148656022 | |||||||
| chr2:148656022 | T | TG | 5 | a0001c0001t0001g0012 a0001c0001t0001g0251 a0001c0001t0001g0292 others(2): Show |
5 | HG02723.hp1 HG03130.hp2 NA18960.hp2 others(2): Show |
intron_variant | MODIFIER | c.153+10853dupG | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148656022 | ||||||
| chr2:148656024 | T | G | 20 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0188 others(17): Show |
20 | HG00642.hp1 HG01517.hp1 HG02004.hp1 others(17): Show |
intron_variant | MODIFIER | c.153+10854T>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148656024 | |||||||
| chr2:148656024 | T | TGTGTGTG others(3): Show |
1 | a0001c0001t0001g0282 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.153+10855_153+1085 others(14): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148656024 | ||||||
| chr2:148656025 | G | GT | 41 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0146 others(38): Show |
42 | HG00423.hp1 HG00544.hp1 HG01070.hp1 others(39): Show |
intron_variant | MODIFIER | c.153+10855_153+1085 others(5): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148656025 | |||||||
| chr2:148656025 | G | GTGT | 12 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(9): Show |
12 | HG02080.hp1 HG02145.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.153+10855_153+1085 others(7): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148656025 | |||||||
| chr2:148656025 | G | GTGTGTGT others(4): Show |
1 | a0001c0001t0002g0113 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.153+10855_153+1085 others(15): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148656025 | |||||||
| chr2:148656026 | G | T | 143 | a0001c0001t0001g0010 a0001c0001t0001g0027 a0001c0001t0001g0029 others(140): Show |
143 | HG00280.hp1 HG00280.hp2 HG00423.hp2 others(140): Show |
intron_variant | MODIFIER | c.153+10856G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148656026 | |||||||
| chr2:148656027 | G | T | 26 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(23): Show |
26 | HG00423.hp1 HG00544.hp1 HG01123.hp1 others(23): Show |
intron_variant | MODIFIER | c.153+10857G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148656027 | |||||||
| chr2:148656028 | G | T | 112 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(109): Show |
112 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(109): Show |
intron_variant | MODIFIER | c.153+10858G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148656028 | |||||||
| chr2:148656029 | G | T | 2 | a0001c0001t0001g0154 a0001c0001t0002g0113 |
2 | NA18985.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.153+10859G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148656029 | |||||||
| chr2:148656030 | G | T | 103 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(100): Show |
103 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(100): Show |
intron_variant | MODIFIER | c.153+10860G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148656030 | |||||||
| chr2:148656031 | G | T | 2 | a0001c0001t0001g0154 a0001c0001t0002g0113 |
2 | NA18985.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.153+10861G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148656031 | |||||||
| chr2:148656032 | G | T | 103 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(100): Show |
103 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(100): Show |
intron_variant | MODIFIER | c.153+10862G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148656032 | |||||||
| chr2:148656033 | G | T | 1 | a0001c0001t0002g0113 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.153+10863G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148656033 | |||||||
| chr2:148656034 | G | T | 102 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(99): Show |
102 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(99): Show |
intron_variant | MODIFIER | c.153+10864G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148656034 | |||||||
| chr2:148656035 | G | T | 1 | a0001c0001t0002g0113 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.153+10865G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148656035 | |||||||
| chr2:148656036 | G | T | 5 | a0001c0001t0002g0115 a0001c0001t0002g0116 a0001c0001t0002g0117 others(2): Show |
5 | HG00423.hp2 HG02135.hp2 NA18956.hp2 others(2): Show |
intron_variant | MODIFIER | c.153+10866G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148656036 | |||||||
| chr2:148656171 | G | A | 1 | a0001c0001t0004g0176 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.153+11001G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148656171 | |||||||
| chr2:148656187 | A | G | 3 | a0001c0001t0001g0250 a0001c0001t0001g0251 a0001c0001t0001g0252 |
3 | HG02572.hp2 HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.153+11017A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148656187 | |||||||
| chr2:148656200 | A | G | 4 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0165 others(1): Show |
4 | NA18939.hp2 NA18945.hp2 NA18956.hp1 others(1): Show |
intron_variant | MODIFIER | c.153+11030A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148656200 | |||||||
| chr2:148656403 | AAAAT | A | 105 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(102): Show |
105 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(102): Show |
intron_variant | MODIFIER | c.153+11234_153+1123 others(8): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148656403 | |||||||
| chr2:148656477 | A | T | 3 | a0001c0001t0001g0036 a0001c0001t0001g0042 a0001c0001t0001g0043 |
3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.153+11307A>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148656477 | |||||||
| chr2:148656539 | T | C | 2 | a0001c0001t0001g0281 a0001c0001t0001g0282 |
2 | HG02257.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.153+11369T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148656539 | |||||||
| chr2:148656620 | A | G | 1 | a0001c0001t0002g0097 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.153+11450A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148656620 | |||||||
| chr2:148656737 | C | T | 6 | a0001c0001t0001g0274 a0001c0001t0001g0275 a0001c0001t0001g0276 others(3): Show |
6 | HG02572.hp1 HG02615.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.153+11567C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148656737 | |||||||
| chr2:148656870 | A | G | 168 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(165): Show |
169 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(166): Show |
intron_variant | MODIFIER | c.153+11700A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148656870 | |||||||
| chr2:148656881 | G | A | 9 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(6): Show |
9 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.153+11711G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148656881 | |||||||
| chr2:148656970 | A | G | 3 | a0001c0001t0001g0250 a0001c0001t0001g0251 a0001c0001t0001g0252 |
3 | HG02572.hp2 HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.153+11800A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148656970 | |||||||
| chr2:148657175 | G | A | 1 | a0001c0001t0001g0134 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.153+12005G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148657175 | |||||||
| chr2:148657319 | T | G | 1 | a0001c0001t0003g0062 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.153+12149T>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148657319 | |||||||
| chr2:148657358 | A | G | 1 | a0001c0001t0001g0167 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.153+12188A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148657358 | |||||||
| chr2:148657377 | A | C | 95 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(92): Show |
95 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.153+12207A>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148657377 | |||||||
| chr2:148657440 | A | G | 1 | a0001c0001t0001g0030 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.153+12270A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148657440 | |||||||
| chr2:148657487 | C | T | 1 | a0001c0001t0001g0277 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.153+12317C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148657487 | |||||||
| chr2:148657549 | A | G | 1 | a0001c0001t0001g0025 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.153+12379A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148657549 | |||||||
| chr2:148657586 | T | G | 35 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0178 others(32): Show |
36 | HG00544.hp2 HG00609.hp2 HG00673.hp2 others(33): Show |
intron_variant | MODIFIER | c.153+12416T>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148657586 | |||||||
| chr2:148657768 | C | T | 2 | a0001c0001t0001g0023 a0001c0001t0001g0024 |
2 | HG02922.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.153+12598C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148657768 | |||||||
| chr2:148657796 | G | A | 1 | a0001c0001t0001g0025 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.153+12626G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148657796 | |||||||
| chr2:148657859 | A | G | 1 | a0001c0001t0001g0195 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.153+12689A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148657859 | |||||||
| chr2:148657884 | T | TTG | 50 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(47): Show |
50 | HG00280.hp2 HG00642.hp2 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.153+12736_153+1273 others(6): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148657884 | ||||||
| chr2:148657884 | T | TTGTG | 69 | a0001c0001t0001g0031 a0001c0001t0002g0037 a0001c0001t0002g0040 others(66): Show |
69 | HG00423.hp2 HG00558.hp2 HG00741.hp1 others(66): Show |
intron_variant | MODIFIER | c.153+12734_153+1273 others(8): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148657884 | ||||||
| chr2:148657973 | C | T | 3 | a0001c0001t0002g0063 a0001c0001t0002g0095 a0001c0001t0002g0096 |
3 | HG00673.hp1 HG02040.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.153+12803C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148657973 | |||||||
| chr2:148658016 | G | A | 1 | a0001c0001t0002g0098 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.153+12846G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148658016 | |||||||
| chr2:148658060 | G | A | 1 | a0001c0001t0002g0060 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.153+12890G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148658060 | |||||||
| chr2:148658087 | A | T | 94 | a0001c0001t0001g0036 a0001c0001t0001g0042 a0001c0001t0001g0043 others(91): Show |
94 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(91): Show |
intron_variant | MODIFIER | c.153+12917A>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148658087 | |||||||
| chr2:148658150 | G | A | 2 | a0001c0001t0001g0171 a0001c0001t0001g0241 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.153+12980G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148658150 | |||||||
| chr2:148658311 | C | T | 108 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(105): Show |
108 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(105): Show |
intron_variant | MODIFIER | c.153+13141C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148658311 | |||||||
| chr2:148658342 | C | A | 1 | a0001c0001t0002g0122 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.153+13172C>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148658342 | |||||||
| chr2:148658503 | G | A | 4 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(1): Show |
4 | HG00639.hp2 HG02809.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.153+13333G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148658503 | |||||||
| chr2:148658552 | G | A | 4 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0001g0184 others(1): Show |
4 | NA18954.hp2 NA19001.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.153+13382G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148658552 | |||||||
| chr2:148658593 | CTG | C | 7 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(4): Show |
7 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(4): Show |
intron_variant | MODIFIER | c.153+13437_153+1343 others(6): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148658593 | ||||||
| chr2:148658605 | GTGTA | G | 13 | a0001c0001t0001g0171 a0001c0001t0001g0189 a0001c0001t0001g0190 others(10): Show |
13 | HG00639.hp1 HG02109.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.153+13437_153+1344 others(8): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148658605 | ||||||
| chr2:148658607 | G | A | 7 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(4): Show |
7 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(4): Show |
intron_variant | MODIFIER | c.153+13437G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148658607 | |||||||
| chr2:148658607 | G | GTA | 19 | a0001c0001t0001g0012 a0001c0001t0001g0015 a0001c0001t0001g0021 others(16): Show |
19 | HG00673.hp2 HG01943.hp1 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.153+13461_153+1346 others(6): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148658607 | ||||||
| chr2:148658607 | G | GTATA | 23 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0001g0184 others(20): Show |
23 | HG00738.hp2 HG01069.hp1 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.153+13459_153+1346 others(8): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148658607 | ||||||
| chr2:148658607 | G | GTATATA | 20 | a0001c0001t0001g0290 a0001c0001t0002g0050 a0001c0001t0002g0052 others(17): Show |
20 | HG00558.hp2 HG01123.hp2 HG01981.hp2 others(17): Show |
intron_variant | MODIFIER | c.153+13457_153+1346 others(10): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148658607 | ||||||
| chr2:148658607 | G | GTATATAT others(1): Show |
19 | a0001c0001t0002g0041 a0001c0001t0002g0064 a0001c0001t0002g0065 others(16): Show |
19 | HG00280.hp2 HG00642.hp2 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.153+13455_153+1346 others(12): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148658607 | ||||||
| chr2:148658607 | G | GTATATAT others(3): Show |
9 | a0001c0001t0002g0067 a0001c0001t0002g0069 a0001c0001t0002g0082 others(6): Show |
9 | HG01884.hp2 HG02040.hp1 HG02071.hp2 others(6): Show |
intron_variant | MODIFIER | c.153+13453_153+1346 others(14): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148658607 | ||||||
| chr2:148658607 | G | GTATATAT others(7): Show |
2 | a0001c0001t0002g0063 a0001c0001t0002g0075 |
2 | HG00673.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.153+13449_153+1346 others(18): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148658607 | ||||||
| chr2:148658607 | G | GTATATAT others(9): Show |
4 | a0001c0001t0002g0038 a0001c0001t0002g0040 a0001c0001t0002g0070 others(1): Show |
4 | HG00735.hp1 HG03704.hp2 NA18950.hp2 others(1): Show |
intron_variant | MODIFIER | c.153+13447_153+1346 others(20): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148658607 | ||||||
| chr2:148658607 | G | GTATATAT others(11): Show |
2 | a0001c0001t0002g0080 a0001c0001t0002g0098 |
2 | NA19065.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.153+13445_153+1346 others(22): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148658607 | ||||||
| chr2:148658607 | G | GTATATAT others(13): Show |
1 | a0001c0001t0002g0113 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.153+13443_153+1346 others(24): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148658607 | ||||||
| chr2:148658607 | G | GTGTA | 5 | a0001c0001t0002g0054 a0001c0001t0002g0115 a0001c0001t0002g0116 others(2): Show |
5 | HG00423.hp2 HG02135.hp2 HG03927.hp2 others(2): Show |
intron_variant | MODIFIER | c.153+13438_153+1343 others(8): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148658607 | ||||||
| chr2:148658607 | G | GTGTATA | 12 | a0001c0001t0002g0053 a0001c0001t0002g0055 a0001c0001t0002g0056 others(9): Show |
12 | HG00741.hp1 HG01106.hp1 HG01258.hp1 others(9): Show |
intron_variant | MODIFIER | c.153+13438_153+1343 others(10): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148658607 | ||||||
| chr2:148658607 | GTA | G | 28 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(25): Show |
29 | HG00544.hp2 HG00609.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.153+13461_153+1346 others(6): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148658607 | ||||||
| chr2:148658607 | GTATA | G | 72 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(69): Show |
72 | HG00280.hp1 HG00609.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.153+13459_153+1346 others(8): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148658607 | ||||||
| chr2:148658607 | GTATATA | G | 56 | a0001c0001t0001g0129 a0001c0001t0001g0131 a0001c0001t0001g0132 others(53): Show |
56 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(53): Show |
intron_variant | MODIFIER | c.153+13457_153+1346 others(10): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148658607 | ||||||
| chr2:148658611 | A | G | 22 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(19): Show |
23 | HG00544.hp2 HG00609.hp2 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.153+13441A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148658611 | |||||||
| chr2:148658613 | A | G | 70 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(67): Show |
70 | HG00280.hp1 HG00609.hp1 HG00642.hp1 others(67): Show |
intron_variant | MODIFIER | c.153+13443A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148658613 | |||||||
| chr2:148658615 | A | G | 105 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(102): Show |
105 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(102): Show |
intron_variant | MODIFIER | c.153+13445A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148658615 | |||||||
| chr2:148658617 | A | G | 2 | a0001c0001t0001g0195 a0001c0001t0001g0265 |
2 | HG03098.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.153+13447A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148658617 | |||||||
| chr2:148658776 | TTAC | T | 3 | a0001c0001t0001g0232 a0001c0001t0001g0263 a0001c0001t0001g0264 |
3 | NA18612.hp2 NA18975.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.153+13611_153+1361 others(7): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148658776 | ||||||
| chr2:148658819 | ATATG | A | 6 | a0001c0001t0001g0267 a0001c0001t0001g0271 a0001c0001t0001g0272 others(3): Show |
6 | HG01884.hp1 HG02109.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.153+13655_153+1365 others(8): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148658819 | ||||||
| chr2:148658982 | C | G | 1 | a0001c0001t0002g0060 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.153+13812C>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148658982 | |||||||
| chr2:148659251 | G | A | 4 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(1): Show |
4 | HG02145.hp1 HG02451.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.153+14081G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148659251 | |||||||
| chr2:148659252 | C | G | 4 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(1): Show |
4 | HG00639.hp2 HG02809.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.153+14082C>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148659252 | |||||||
| chr2:148659436 | T | C | 94 | a0001c0001t0001g0036 a0001c0001t0001g0042 a0001c0001t0001g0043 others(91): Show |
94 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(91): Show |
intron_variant | MODIFIER | c.153+14266T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148659436 | |||||||
| chr2:148659820 | GACATTA | G | 11 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0178 others(8): Show |
12 | HG00544.hp2 HG00609.hp2 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.153+14654_153+1465 others(10): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148659820 | ||||||
| chr2:148659889 | G | T | 108 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(105): Show |
108 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(105): Show |
intron_variant | MODIFIER | c.153+14719G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148659889 | |||||||
| chr2:148659903 | T | G | 4 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(1): Show |
4 | HG00639.hp2 HG02809.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.153+14733T>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148659903 | |||||||
| chr2:148660055 | A | C | 2 | a0001c0001t0003g0094 a0001c0001t0003g0121 |
2 | HG01981.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.153+14885A>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148660055 | |||||||
| chr2:148660184 | C | A | 105 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(102): Show |
105 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(102): Show |
intron_variant | MODIFIER | c.153+15014C>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148660184 | |||||||
| chr2:148660299 | T | C | 1 | a0001c0001t0001g0033 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.153+15129T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148660299 | |||||||
| chr2:148660335 | G | A | 1 | a0001c0001t0001g0279 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.153+15165G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148660335 | |||||||
| chr2:148660340 | G | T | 18 | a0001c0001t0002g0053 a0001c0001t0002g0054 a0001c0001t0002g0055 others(15): Show |
18 | HG00280.hp2 HG00642.hp2 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.153+15170G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148660340 | |||||||
| chr2:148660473 | A | G | 10 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(7): Show |
10 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(7): Show |
intron_variant | MODIFIER | c.153+15303A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148660473 | |||||||
| chr2:148660537 | A | C | 2 | a0001c0001t0001g0281 a0001c0001t0001g0282 |
2 | HG02257.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.153+15367A>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148660537 | |||||||
| chr2:148660573 | G | GT | 6 | a0001c0001t0001g0188 a0001c0001t0001g0216 a0001c0001t0001g0250 others(3): Show |
6 | HG00642.hp1 HG02572.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.153+15416dupT | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148660573 | ||||||
| chr2:148660586 | T | A | 11 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0178 others(8): Show |
12 | HG00544.hp2 HG00609.hp2 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.153+15416T>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148660586 | |||||||
| chr2:148660605 | G | T | 1 | a0001c0001t0001g0043 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.153+15435G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148660605 | |||||||
| chr2:148660606 | C | T | 1 | a0001c0001t0001g0043 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.153+15436C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148660606 | |||||||
| chr2:148660680 | T | G | 1 | a0001c0001t0001g0279 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.153+15510T>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148660680 | |||||||
| chr2:148660706 | T | A | 1 | a0001c0001t0002g0127 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.153+15536T>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148660706 | |||||||
| chr2:148661056 | T | C | 1 | a0001c0005t0001g0186 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.153+15886T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148661056 | |||||||
| chr2:148661068 | T | C | 1 | a0001c0001t0001g0200 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.153+15898T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148661068 | |||||||
| chr2:148661130 | C | T | 10 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(7): Show |
10 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(7): Show |
intron_variant | MODIFIER | c.153+15960C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148661130 | |||||||
| chr2:148661202 | T | C | 2 | a0001c0004t0001g0013 a0001c0004t0001g0026 |
2 | HG01891.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.153+16032T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148661202 | |||||||
| chr2:148661234 | A | G | 1 | a0001c0001t0002g0122 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.153+16064A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148661234 | |||||||
| chr2:148661403 | C | A | 108 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(105): Show |
108 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(105): Show |
intron_variant | MODIFIER | c.153+16233C>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148661403 | |||||||
| chr2:148661522 | T | C | 290 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(287): Show |
291 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(288): Show |
intron_variant | MODIFIER | c.153+16352T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148661522 | |||||||
| chr2:148661626 | C | G | 111 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(108): Show |
111 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(108): Show |
intron_variant | MODIFIER | c.153+16456C>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148661626 | |||||||
| chr2:148661635 | G | A | 91 | a0001c0001t0002g0037 a0001c0001t0002g0038 a0001c0001t0002g0040 others(88): Show |
91 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.153+16465G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148661635 | |||||||
| chr2:148661640 | G | A | 2 | a0001c0001t0002g0064 a0001c0001t0002g0065 |
2 | NA18941.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.153+16470G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148661640 | |||||||
| chr2:148661661 | A | G | 1 | a0001c0001t0002g0058 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.153+16491A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148661661 | |||||||
| chr2:148661667 | A | G | 1 | a0001c0001t0001g0267 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.153+16497A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148661667 | |||||||
| chr2:148661695 | T | TTATG | 108 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(105): Show |
108 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(105): Show |
intron_variant | MODIFIER | c.153+16528_153+1653 others(8): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148661695 | ||||||
| chr2:148661772 | A | G | 11 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0178 others(8): Show |
12 | HG00544.hp2 HG00609.hp2 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.153+16602A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148661772 | |||||||
| chr2:148661866 | C | T | 1 | a0001c0005t0001g0009 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.153+16696C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148661866 | |||||||
| chr2:148662058 | A | G | 10 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(7): Show |
10 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(7): Show |
intron_variant | MODIFIER | c.153+16888A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148662058 | |||||||
| chr2:148662059 | T | C | 4 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(1): Show |
4 | HG02145.hp1 HG02451.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.153+16889T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148662059 | |||||||
| chr2:148662079 | C | G | 111 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0134 others(108): Show |
111 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(108): Show |
intron_variant | MODIFIER | c.153+16909C>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148662079 | |||||||
| chr2:148662222 | G | T | 290 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(287): Show |
291 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(288): Show |
intron_variant | MODIFIER | c.153+17052G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148662222 | |||||||
| chr2:148662250 | T | A | 9 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(6): Show |
9 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.153+17080T>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148662250 | |||||||
| chr2:148662271 | G | A | 17 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(14): Show |
17 | HG00639.hp2 HG02040.hp2 HG02132.hp1 others(14): Show |
intron_variant | MODIFIER | c.153+17101G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148662271 | |||||||
| chr2:148662401 | A | G | 2 | a0001c0001t0001g0281 a0001c0001t0001g0282 |
2 | HG02257.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.153+17231A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148662401 | |||||||
| chr2:148662421 | C | T | 1 | a0001c0001t0001g0228 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.153+17251C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148662421 | |||||||
| chr2:148662495 | T | C | 1 | a0001c0001t0001g0028 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.153+17325T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148662495 | |||||||
| chr2:148662501 | G | C | 10 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(7): Show |
10 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(7): Show |
intron_variant | MODIFIER | c.153+17331G>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148662501 | |||||||
| chr2:148662561 | G | A | 11 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0178 others(8): Show |
12 | HG00544.hp2 HG00609.hp2 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.153+17391G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148662561 | |||||||
| chr2:148662616 | A | G | 20 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0001g0184 others(17): Show |
20 | HG00673.hp2 HG02074.hp2 HG04204.hp1 others(17): Show |
intron_variant | MODIFIER | c.153+17446A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148662616 | |||||||
| chr2:148662619 | A | T | 1 | a0001c0001t0001g0238 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.153+17449A>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148662619 | |||||||
| chr2:148662705 | A | T | 1 | a0001c0001t0001g0250 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.153+17535A>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148662705 | |||||||
| chr2:148662812 | T | TATA | 129 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0134 others(126): Show |
129 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(126): Show |
intron_variant | MODIFIER | c.153+17653_153+1765 others(7): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148662812 | ||||||
| chr2:148662828 | T | A | 9 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(6): Show |
9 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.153+17658T>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148662828 | |||||||
| chr2:148662834 | T | A | 1 | a0001c0001t0001g0240 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.153+17664T>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148662834 | |||||||
| chr2:148662835 | A | T | 1 | a0001c0001t0001g0289 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.153+17665A>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148662835 | |||||||
| chr2:148662989 | T | A | 1 | a0001c0001t0001g0289 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.153+17819T>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148662989 | |||||||
| chr2:148663038 | T | G | 91 | a0001c0001t0002g0037 a0001c0001t0002g0038 a0001c0001t0002g0040 others(88): Show |
91 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.153+17868T>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148663038 | |||||||
| chr2:148663193 | T | TTTA | 3 | a0001c0001t0004g0173 a0001c0001t0004g0177 a0001c0001t0004g0181 |
3 | HG00544.hp2 HG00609.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.153+18023_153+1802 others(7): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148663193 | |||||||
| chr2:148663194 | G | GTAT | 61 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0027 others(58): Show |
61 | HG00280.hp2 HG00639.hp1 HG00673.hp1 others(58): Show |
intron_variant | MODIFIER | c.153+18068_153+1807 others(7): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148663194 | ||||||
| chr2:148663194 | G | GTATTAT | 36 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0033 others(33): Show |
36 | HG00609.hp1 HG00642.hp1 HG00741.hp2 others(33): Show |
intron_variant | MODIFIER | c.153+18065_153+1807 others(10): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148663194 | ||||||
| chr2:148663194 | G | GTATTATT others(2): Show |
21 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0029 others(18): Show |
21 | HG00280.hp1 HG00738.hp1 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.153+18062_153+1807 others(13): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148663194 | ||||||
| chr2:148663194 | G | GTATTATT others(5): Show |
2 | a0001c0001t0001g0197 a0001c0001t0002g0053 |
2 | HG01258.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.153+18059_153+1807 others(16): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148663194 | ||||||
| chr2:148663194 | G | T | 11 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0178 others(8): Show |
12 | HG00544.hp2 HG00609.hp2 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.153+18024G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148663194 | |||||||
| chr2:148663194 | GTAT | G | 53 | a0001c0001t0001g0012 a0001c0001t0001g0021 a0001c0001t0001g0022 others(50): Show |
53 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(50): Show |
intron_variant | MODIFIER | c.153+18068_153+1807 others(7): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148663194 | ||||||
| chr2:148663194 | GTATTAT | G | 67 | a0001c0001t0001g0140 a0001c0001t0001g0152 a0001c0001t0001g0167 others(64): Show |
67 | HG00423.hp2 HG00558.hp2 HG00738.hp2 others(64): Show |
intron_variant | MODIFIER | c.153+18065_153+1807 others(10): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148663194 | ||||||
| chr2:148663194 | GTATTATT others(2): Show |
G | 8 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(5): Show |
8 | HG02145.hp1 HG02451.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.153+18062_153+1807 others(13): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148663194 | ||||||
| chr2:148663194 | GTATTATT others(5): Show |
G | 4 | a0001c0001t0002g0052 a0001c0001t0002g0061 a0001c0001t0002g0092 others(1): Show |
4 | HG03654.hp2 HG03942.hp1 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.153+18059_153+1807 others(16): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148663194 | ||||||
| chr2:148663346 | G | A | 20 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0001g0184 others(17): Show |
20 | HG00673.hp2 HG02074.hp2 HG04204.hp1 others(17): Show |
intron_variant | MODIFIER | c.153+18176G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148663346 | |||||||
| chr2:148663411 | G | T | 1 | a0001c0001t0001g0256 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.153+18241G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148663411 | |||||||
| chr2:148663575 | T | C | 2 | a0001c0001t0001g0144 a0001c0001t0001g0145 |
2 | HG00558.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.153+18405T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148663575 | |||||||
| chr2:148663581 | T | C | 3 | a0001c0001t0001g0036 a0001c0001t0001g0042 a0001c0001t0001g0043 |
3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.153+18411T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148663581 | |||||||
| chr2:148663592 | A | AT | 7 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0020 others(4): Show |
7 | HG01891.hp1 HG02145.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.153+18450dupT | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148663592 | ||||||
| chr2:148663592 | AT | A | 66 | a0001c0001t0001g0036 a0001c0001t0001g0042 a0001c0001t0001g0043 others(63): Show |
66 | HG00423.hp1 HG00609.hp1 HG00673.hp2 others(63): Show |
intron_variant | MODIFIER | c.153+18450delT | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148663592 | ||||||
| chr2:148663592 | ATT | A | 164 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0134 others(161): Show |
164 | HG00280.hp1 HG00280.hp2 HG00423.hp2 others(161): Show |
intron_variant | MODIFIER | c.153+18449_153+1845 others(6): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148663592 | ||||||
| chr2:148663592 | ATTTTTTT | A | 8 | a0001c0001t0001g0250 a0001c0001t0001g0251 a0001c0001t0001g0252 others(5): Show |
8 | HG01884.hp1 HG02109.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.153+18444_153+1845 others(11): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148663592 | ||||||
| chr2:148663592 | ATTTTTTT others(1): Show |
A | 12 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0178 others(9): Show |
13 | HG00544.hp2 HG00609.hp2 HG01106.hp2 others(10): Show |
intron_variant | MODIFIER | c.153+18443_153+1845 others(12): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148663592 | ||||||
| chr2:148663592 | ATTTTTTT others(2): Show |
A | 9 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(6): Show |
9 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.153+18442_153+1845 others(13): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148663592 | ||||||
| chr2:148663592 | ATTTTTTT others(5): Show |
A | 1 | a0001c0001t0001g0304 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.153+18439_153+1845 others(16): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148663592 | ||||||
| chr2:148663643 | G | GAA | 3 | a0001c0001t0001g0250 a0001c0001t0001g0251 a0001c0001t0001g0252 |
3 | HG02572.hp2 HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.153+18474_153+1847 others(6): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148663643 | ||||||
| chr2:148663690 | C | G | 1 | a0001c0001t0002g0052 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.153+18520C>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148663690 | |||||||
| chr2:148663783 | C | T | 1 | a0001c0001t0001g0304 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.153+18613C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148663783 | |||||||
| chr2:148663875 | A | G | 3 | a0001c0001t0002g0055 a0001c0001t0002g0056 a0001c0001t0002g0057 |
3 | HG01106.hp1 HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.153+18705A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148663875 | |||||||
| chr2:148663879 | T | A | 3 | a0001c0001t0001g0036 a0001c0001t0001g0042 a0001c0001t0001g0043 |
3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.153+18709T>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148663879 | |||||||
| chr2:148663934 | C | G | 5 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0001c0003t0001g0249 others(2): Show |
5 | HG01884.hp1 HG02109.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.153+18764C>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148663934 | |||||||
| chr2:148663981 | C | A | 1 | a0001c0001t0001g0028 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.153+18811C>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148663981 | |||||||
| chr2:148664342 | T | C | 3 | a0001c0001t0001g0036 a0001c0001t0001g0042 a0001c0001t0001g0043 |
3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.153+19172T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148664342 | |||||||
| chr2:148664458 | G | A | 108 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(105): Show |
108 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(105): Show |
intron_variant | MODIFIER | c.153+19288G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148664458 | |||||||
| chr2:148664558 | A | G | 3 | a0001c0001t0002g0088 a0001c0001t0002g0089 a0001c0001t0002g0091 |
3 | NA18975.hp1 NA19077.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.153+19388A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148664558 | |||||||
| chr2:148664981 | G | C | 1 | a0002c0002t0006g0254 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.153+19811G>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148664981 | |||||||
| chr2:148665188 | G | C | 1 | a0001c0001t0001g0178 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.153+20018G>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148665188 | |||||||
| chr2:148665358 | A | C | 1 | a0001c0001t0001g0250 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.153+20188A>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148665358 | |||||||
| chr2:148665475 | A | G | 1 | a0001c0001t0001g0276 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.153+20305A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148665475 | |||||||
| chr2:148665521 | G | C | 2 | a0001c0001t0001g0251 a0001c0001t0001g0252 |
2 | HG02572.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.153+20351G>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148665521 | |||||||
| chr2:148665683 | T | A | 3 | a0001c0001t0001g0036 a0001c0001t0001g0042 a0001c0001t0001g0043 |
3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.153+20513T>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148665683 | |||||||
| chr2:148665762 | A | G | 1 | a0001c0001t0001g0175 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.153+20592A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148665762 | |||||||
| chr2:148665818 | C | T | 9 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(6): Show |
9 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.153+20648C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148665818 | |||||||
| chr2:148665907 | A | G | 1 | a0001c0001t0001g0304 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.153+20737A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148665907 | |||||||
| chr2:148666078 | G | A | 12 | a0001c0001t0001g0201 a0001c0001t0001g0213 a0001c0001t0001g0232 others(9): Show |
12 | HG00609.hp1 HG01346.hp2 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.153+20908G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148666078 | |||||||
| chr2:148666201 | C | T | 2 | a0001c0001t0001g0042 a0001c0001t0001g0043 |
2 | HG02145.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.153+21031C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148666201 | |||||||
| chr2:148666465 | T | A | 1 | a0001c0003t0001g0249 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.153+21295T>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148666465 | |||||||
| chr2:148666530 | T | C | 1 | a0001c0005t0001g0009 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.153+21360T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148666530 | |||||||
| chr2:148666563 | A | G | 1 | a0001c0001t0002g0058 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.153+21393A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148666563 | |||||||
| chr2:148666687 | T | C | 1 | a0001c0001t0001g0194 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.153+21517T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148666687 | |||||||
| chr2:148666768 | A | G | 1 | a0001c0001t0001g0003 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.153+21598A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148666768 | |||||||
| chr2:148666851 | T | C | 1 | a0001c0001t0001g0300 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.153+21681T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148666851 | |||||||
| chr2:148666853 | A | G | 10 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(7): Show |
10 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(7): Show |
intron_variant | MODIFIER | c.153+21683A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148666853 | |||||||
| chr2:148666869 | CT | C | 274 | a0001c0001t0001g0008 a0001c0001t0001g0028 a0001c0001t0001g0036 others(271): Show |
275 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(272): Show |
intron_variant | MODIFIER | c.153+21714delT | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148666869 | ||||||
| chr2:148666961 | T | A | 1 | a0001c0001t0001g0036 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.153+21791T>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148666961 | |||||||
| chr2:148667137 | C | G | 10 | a0001c0001t0001g0274 a0001c0001t0001g0275 a0001c0001t0001g0276 others(7): Show |
10 | HG02257.hp1 HG02257.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.153+21967C>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148667137 | |||||||
| chr2:148667235 | T | G | 1 | a0001c0001t0001g0245 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.153+22065T>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148667235 | |||||||
| chr2:148667356 | G | C | 108 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(105): Show |
108 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(105): Show |
intron_variant | MODIFIER | c.153+22186G>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148667356 | |||||||
| chr2:148667400 | T | A | 1 | a0001c0001t0001g0265 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.153+22230T>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148667400 | |||||||
| chr2:148667420 | G | T | 9 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(6): Show |
9 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.153+22250G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148667420 | |||||||
| chr2:148667513 | G | GT | 6 | a0001c0001t0002g0058 a0001c0001t0002g0067 a0001c0005t0001g0186 others(3): Show |
6 | HG02647.hp2 HG02965.hp1 HG03831.hp2 others(3): Show |
intron_variant | MODIFIER | c.153+22352dupT | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148667513 | ||||||
| chr2:148667827 | G | C | 95 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(92): Show |
95 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.154-22387G>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148667827 | |||||||
| chr2:148668105 | G | A | 1 | a0001c0001t0001g0240 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.154-22109G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148668105 | |||||||
| chr2:148668616 | G | A | 1 | a0001c0001t0001g0304 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.154-21598G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148668616 | |||||||
| chr2:148668630 | G | T | 1 | a0001c0001t0001g0304 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.154-21584G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148668630 | |||||||
| chr2:148668666 | G | A | 2 | a0001c0001t0002g0106 a0001c0001t0002g0107 |
2 | NA18969.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.154-21548G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148668666 | |||||||
| chr2:148668852 | A | C | 1 | a0001c0001t0001g0267 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.154-21362A>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148668852 | |||||||
| chr2:148668864 | G | T | 108 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(105): Show |
108 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(105): Show |
intron_variant | MODIFIER | c.154-21350G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148668864 | |||||||
| chr2:148668892 | T | G | 3 | a0001c0001t0001g0250 a0001c0001t0001g0251 a0001c0001t0001g0252 |
3 | HG02572.hp2 HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.154-21322T>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148668892 | |||||||
| chr2:148668894 | T | G | 91 | a0001c0001t0002g0037 a0001c0001t0002g0038 a0001c0001t0002g0040 others(88): Show |
91 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.154-21320T>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148668894 | |||||||
| chr2:148668975 | A | G | 1 | a0001c0001t0002g0114 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.154-21239A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148668975 | |||||||
| chr2:148669002 | A | G | 111 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0134 others(108): Show |
111 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(108): Show |
intron_variant | MODIFIER | c.154-21212A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148669002 | |||||||
| chr2:148669205 | G | A | 91 | a0001c0001t0002g0037 a0001c0001t0002g0038 a0001c0001t0002g0040 others(88): Show |
91 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.154-21009G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148669205 | |||||||
| chr2:148669428 | G | A | 6 | a0001c0001t0001g0267 a0001c0001t0001g0271 a0001c0001t0001g0272 others(3): Show |
6 | HG01884.hp1 HG02109.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.154-20786G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148669428 | |||||||
| chr2:148669673 | A | G | 1 | a0002c0002t0001g0307 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.154-20541A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148669673 | |||||||
| chr2:148669683 | C | T | 3 | a0001c0001t0001g0250 a0001c0001t0001g0251 a0001c0001t0001g0252 |
3 | HG02572.hp2 HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.154-20531C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148669683 | |||||||
| chr2:148669703 | C | G | 8 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(5): Show |
8 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(5): Show |
intron_variant | MODIFIER | c.154-20511C>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148669703 | |||||||
| chr2:148669735 | T | C | 5 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0191 others(2): Show |
5 | HG02258.hp1 HG02886.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.154-20479T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148669735 | |||||||
| chr2:148669804 | A | G | 1 | a0001c0001t0001g0175 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.154-20410A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148669804 | |||||||
| chr2:148669855 | T | G | 10 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(7): Show |
10 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(7): Show |
intron_variant | MODIFIER | c.154-20359T>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148669855 | |||||||
| chr2:148669905 | T | G | 1 | a0001c0001t0001g0028 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.154-20309T>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148669905 | |||||||
| chr2:148669998 | G | C | 108 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(105): Show |
108 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(105): Show |
intron_variant | MODIFIER | c.154-20216G>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148669998 | |||||||
| chr2:148670159 | T | C | 10 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(7): Show |
10 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(7): Show |
intron_variant | MODIFIER | c.154-20055T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148670159 | |||||||
| chr2:148670225 | G | T | 133 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0014 others(130): Show |
133 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(130): Show |
intron_variant | MODIFIER | c.154-19989G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148670225 | |||||||
| chr2:148670321 | AT | A | 10 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(7): Show |
10 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(7): Show |
intron_variant | MODIFIER | c.154-19890delT | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148670321 | ||||||
| chr2:148670331 | T | A | 1 | a0001c0001t0001g0262 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.154-19883T>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148670331 | |||||||
| chr2:148670339 | CT | C | 31 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(28): Show |
31 | HG00673.hp2 HG01069.hp1 HG02040.hp2 others(28): Show |
intron_variant | MODIFIER | c.154-19863delT | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148670339 | ||||||
| chr2:148670506 | C | T | 1 | a0001c0001t0002g0105 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.154-19708C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148670506 | |||||||
| chr2:148670520 | C | A | 1 | a0001c0001t0001g0152 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.154-19694C>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148670520 | |||||||
| chr2:148670640 | T | A | 4 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(1): Show |
4 | HG00639.hp2 HG02809.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.154-19574T>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148670640 | |||||||
| chr2:148670688 | C | T | 1 | a0001c0001t0001g0276 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.154-19526C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148670688 | |||||||
| chr2:148670791 | C | A | 4 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(1): Show |
4 | HG02145.hp1 HG02451.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.154-19423C>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148670791 | |||||||
| chr2:148670847 | C | T | 3 | a0001c0001t0001g0250 a0001c0001t0001g0251 a0001c0001t0001g0252 |
3 | HG02572.hp2 HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.154-19367C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148670847 | |||||||
| chr2:148670879 | C | T | 22 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0015 others(19): Show |
22 | HG01891.hp1 HG02257.hp1 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.154-19335C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148670879 | |||||||
| chr2:148670923 | A | C | 1 | a0001c0001t0001g0272 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.154-19291A>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148670923 | |||||||
| chr2:148671286 | G | GT | 26 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0178 others(23): Show |
27 | HG00609.hp2 HG00735.hp1 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.154-18928_154-1892 others(5): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148671286 | |||||||
| chr2:148671286 | G | GTT | 3 | a0001c0001t0001g0305 a0001c0001t0002g0049 a0001c0001t0004g0177 |
3 | HG00544.hp2 HG01346.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.154-18928_154-1892 others(6): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148671286 | |||||||
| chr2:148671286 | G | GTTTTT | 3 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0132 |
3 | HG00639.hp2 HG03130.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.154-18928_154-1892 others(9): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148671286 | |||||||
| chr2:148671287 | A | AT | 33 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(30): Show |
33 | HG00280.hp1 HG00609.hp1 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.154-18907dupT | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148671287 | ||||||
| chr2:148671287 | A | ATT | 15 | a0001c0001t0001g0005 a0001c0001t0001g0042 a0001c0001t0001g0043 others(12): Show |
15 | HG01884.hp1 HG02109.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.154-18908_154-1890 others(6): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148671287 | ||||||
| chr2:148671287 | A | ATTT | 17 | a0001c0001t0001g0185 a0001c0001t0001g0216 a0001c0001t0001g0272 others(14): Show |
17 | HG00673.hp2 HG02074.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.154-18909_154-1890 others(7): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148671287 | ||||||
| chr2:148671287 | A | T | 105 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(102): Show |
106 | HG00280.hp2 HG00423.hp2 HG00544.hp2 others(103): Show |
intron_variant | MODIFIER | c.154-18927A>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148671287 | |||||||
| chr2:148671287 | AT | A | 8 | a0001c0001t0001g0028 a0001c0001t0001g0030 a0001c0001t0001g0031 others(5): Show |
8 | HG01981.hp1 HG02155.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.154-18907delT | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148671287 | ||||||
| chr2:148671287 | ATT | A | 16 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0014 others(13): Show |
16 | HG01891.hp1 HG02040.hp2 HG02132.hp1 others(13): Show |
intron_variant | MODIFIER | c.154-18908_154-1890 others(6): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148671287 | ||||||
| chr2:148671310 | A | G | 1 | a0001c0001t0001g0222 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.154-18904A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148671310 | |||||||
| chr2:148671340 | A | T | 22 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0015 others(19): Show |
22 | HG01891.hp1 HG02257.hp1 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.154-18874A>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148671340 | |||||||
| chr2:148671608 | C | A | 3 | a0001c0001t0001g0036 a0001c0001t0001g0042 a0001c0001t0001g0043 |
3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.154-18606C>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148671608 | |||||||
| chr2:148671610 | T | C | 3 | a0001c0001t0001g0152 a0001c0001t0001g0161 a0001c0001t0001g0162 |
3 | HG01123.hp1 HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.154-18604T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148671610 | |||||||
| chr2:148671617 | A | C | 3 | a0001c0001t0001g0152 a0001c0001t0001g0161 a0001c0001t0001g0162 |
3 | HG01123.hp1 HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.154-18597A>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148671617 | |||||||
| chr2:148671731 | G | A | 4 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(1): Show |
4 | HG02145.hp1 HG02451.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.154-18483G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148671731 | |||||||
| chr2:148671847 | A | C | 1 | a0001c0001t0001g0034 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.154-18367A>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148671847 | |||||||
| chr2:148672118 | C | G | 4 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(1): Show |
4 | HG00639.hp2 HG02809.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.154-18096C>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148672118 | |||||||
| chr2:148672635 | C | T | 11 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0015 others(8): Show |
11 | HG01891.hp1 HG02258.hp2 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.154-17579C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148672635 | |||||||
| chr2:148672760 | A | G | 3 | a0001c0001t0001g0152 a0001c0001t0001g0161 a0001c0001t0001g0162 |
3 | HG01123.hp1 HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.154-17454A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148672760 | |||||||
| chr2:148672990 | C | G | 1 | a0001c0001t0001g0134 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.154-17224C>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148672990 | |||||||
| chr2:148673032 | G | A | 6 | a0001c0001t0001g0267 a0001c0001t0001g0271 a0001c0001t0001g0272 others(3): Show |
6 | HG01884.hp1 HG02109.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.154-17182G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148673032 | |||||||
| chr2:148673235 | T | C | 109 | a0001c0001t0001g0036 a0001c0001t0001g0042 a0001c0001t0001g0043 others(106): Show |
110 | HG00280.hp2 HG00423.hp2 HG00544.hp2 others(107): Show |
intron_variant | MODIFIER | c.154-16979T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148673235 | |||||||
| chr2:148673259 | T | C | 1 | a0001c0001t0001g0134 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.154-16955T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148673259 | |||||||
| chr2:148673657 | C | T | 1 | a0001c0001t0001g0259 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.154-16557C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148673657 | |||||||
| chr2:148673902 | T | A | 1 | a0001c0003t0001g0270 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.154-16312T>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148673902 | |||||||
| chr2:148674167 | A | G | 2 | a0001c0001t0001g0030 a0001c0001t0001g0031 |
2 | HG02155.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.154-16047A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148674167 | |||||||
| chr2:148674356 | A | G | 1 | a0001c0001t0001g0167 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.154-15858A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148674356 | |||||||
| chr2:148674376 | C | CAGAATT | 12 | a0001c0001t0001g0171 a0001c0001t0001g0189 a0001c0001t0001g0190 others(9): Show |
12 | HG00639.hp1 HG02109.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.154-15835_154-1583 others(10): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148674376 | ||||||
| chr2:148674510 | A | G | 4 | a0001c0001t0002g0060 a0001c0001t0002g0125 a0001c0001t0002g0126 others(1): Show |
4 | HG02027.hp1 HG02602.hp1 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.154-15704A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148674510 | |||||||
| chr2:148674576 | C | T | 1 | a0001c0001t0002g0093 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.154-15638C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148674576 | |||||||
| chr2:148674641 | G | C | 290 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(287): Show |
291 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(288): Show |
intron_variant | MODIFIER | c.154-15573G>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148674641 | |||||||
| chr2:148674908 | C | G | 2 | a0001c0001t0002g0095 a0001c0001t0002g0096 |
2 | HG02040.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.154-15306C>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148674908 | |||||||
| chr2:148674929 | C | T | 3 | a0001c0001t0001g0137 a0001c0001t0001g0158 a0001c0001t0001g0159 |
3 | NA18969.hp1 NA19001.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.154-15285C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148674929 | |||||||
| chr2:148674933 | G | A | 105 | a0001c0001t0001g0036 a0001c0001t0001g0042 a0001c0001t0001g0043 others(102): Show |
106 | HG00280.hp2 HG00423.hp2 HG00544.hp2 others(103): Show |
intron_variant | MODIFIER | c.154-15281G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148674933 | |||||||
| chr2:148675179 | A | G | 4 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(1): Show |
4 | HG00639.hp2 HG02809.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.154-15035A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148675179 | |||||||
| chr2:148675322 | G | A | 9 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(6): Show |
9 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.154-14892G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148675322 | |||||||
| chr2:148675499 | G | T | 1 | a0001c0001t0002g0069 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.154-14715G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148675499 | |||||||
| chr2:148675501 | T | C | 1 | a0001c0001t0001g0279 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.154-14713T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148675501 | |||||||
| chr2:148675516 | A | G | 109 | a0001c0001t0001g0036 a0001c0001t0001g0042 a0001c0001t0001g0043 others(106): Show |
110 | HG00280.hp2 HG00423.hp2 HG00544.hp2 others(107): Show |
intron_variant | MODIFIER | c.154-14698A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148675516 | |||||||
| chr2:148675705 | T | G | 2 | a0001c0001t0001g0142 a0001c0001t0001g0166 |
2 | HG02080.hp1 NA18948.hp2 |
intron_variant | MODIFIER | c.154-14509T>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148675705 | |||||||
| chr2:148675966 | C | T | 91 | a0001c0001t0002g0037 a0001c0001t0002g0038 a0001c0001t0002g0040 others(88): Show |
91 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.154-14248C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148675966 | |||||||
| chr2:148676079 | C | T | 1 | a0001c0001t0001g0215 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.154-14135C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148676079 | |||||||
| chr2:148676115 | A | C | 2 | a0001c0001t0001g0208 a0001c0001t0001g0219 |
2 | HG00738.hp1 HG01070.hp1 |
intron_variant | MODIFIER | c.154-14099A>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148676115 | |||||||
| chr2:148676127 | G | GT | 107 | a0001c0001t0001g0036 a0001c0001t0001g0043 a0001c0001t0001g0174 others(104): Show |
108 | HG00280.hp2 HG00423.hp2 HG00544.hp2 others(105): Show |
intron_variant | MODIFIER | c.154-14074dupT | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148676127 | ||||||
| chr2:148676127 | GT | G | 12 | a0001c0001t0001g0028 a0001c0001t0001g0035 a0001c0001t0001g0274 others(9): Show |
12 | HG02257.hp1 HG02257.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.154-14074delT | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148676127 | ||||||
| chr2:148676416 | G | A | 3 | a0001c0001t0001g0250 a0001c0001t0001g0251 a0001c0001t0001g0252 |
3 | HG02572.hp2 HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.154-13798G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148676416 | |||||||
| chr2:148676603 | T | C | 6 | a0001c0001t0001g0267 a0001c0001t0001g0271 a0001c0001t0001g0272 others(3): Show |
6 | HG01884.hp1 HG02109.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.154-13611T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148676603 | |||||||
| chr2:148676740 | T | C | 1 | a0001c0001t0001g0218 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.154-13474T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148676740 | |||||||
| chr2:148676768 | C | T | 20 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0001g0184 others(17): Show |
20 | HG00673.hp2 HG02074.hp2 HG04204.hp1 others(17): Show |
intron_variant | MODIFIER | c.154-13446C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148676768 | |||||||
| chr2:148676777 | GCT | G | 162 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(159): Show |
162 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(159): Show |
intron_variant | MODIFIER | c.154-13414_154-1341 others(6): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148676777 | ||||||
| chr2:148676777 | GCTCTCT | G | 114 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(111): Show |
115 | HG00280.hp2 HG00423.hp2 HG00544.hp2 others(112): Show |
intron_variant | MODIFIER | c.154-13418_154-1341 others(10): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148676777 | ||||||
| chr2:148676777 | GCTCTCTC others(3): Show |
G | 1 | a0001c0001t0001g0036 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.154-13422_154-1341 others(14): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148676777 | ||||||
| chr2:148676865 | C | CT | 132 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0010 others(129): Show |
132 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(129): Show |
intron_variant | MODIFIER | c.154-13342dupT | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148676865 | ||||||
| chr2:148676872 | T | TTG | 26 | a0001c0001t0001g0135 a0001c0001t0001g0168 a0001c0001t0001g0189 others(23): Show |
26 | HG00673.hp2 HG02074.hp2 HG02109.hp2 others(23): Show |
intron_variant | MODIFIER | c.154-13342_154-1334 others(6): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148676872 | |||||||
| chr2:148676872 | TG | T | 102 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0178 others(99): Show |
103 | HG00280.hp2 HG00423.hp2 HG00544.hp2 others(100): Show |
intron_variant | MODIFIER | c.154-13332delG | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148676872 | ||||||
| chr2:148676874 | G | GC | 3 | a0001c0001t0001g0250 a0001c0001t0001g0251 a0001c0001t0001g0252 |
3 | HG02572.hp2 HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.154-13340_154-1333 others(5): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148676874 | |||||||
| chr2:148676916 | G | A | 129 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0134 others(126): Show |
129 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(126): Show |
intron_variant | MODIFIER | c.154-13298G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148676916 | |||||||
| chr2:148676961 | A | T | 6 | a0001c0001t0001g0274 a0001c0001t0001g0275 a0001c0001t0001g0276 others(3): Show |
6 | HG02572.hp1 HG02615.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.154-13253A>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148676961 | |||||||
| chr2:148677542 | G | A | 24 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0001g0184 others(21): Show |
24 | HG00673.hp2 HG02074.hp2 HG02647.hp2 others(21): Show |
intron_variant | MODIFIER | c.154-12672G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148677542 | |||||||
| chr2:148677591 | G | A | 4 | a0001c0005t0001g0186 a0002c0002t0001g0253 a0002c0002t0001g0307 others(1): Show |
4 | HG02647.hp2 HG02965.hp1 NA20300.hp1 others(1): Show |
intron_variant | MODIFIER | c.154-12623G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148677591 | |||||||
| chr2:148677615 | C | T | 119 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(116): Show |
120 | HG00280.hp2 HG00423.hp2 HG00544.hp2 others(117): Show |
intron_variant | MODIFIER | c.154-12599C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148677615 | |||||||
| chr2:148677673 | G | A | 102 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0178 others(99): Show |
103 | HG00280.hp2 HG00423.hp2 HG00544.hp2 others(100): Show |
intron_variant | MODIFIER | c.154-12541G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148677673 | |||||||
| chr2:148677694 | T | C | 2 | a0001c0001t0001g0198 a0001c0001t0001g0199 |
2 | HG02818.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.154-12520T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148677694 | |||||||
| chr2:148677770 | G | T | 2 | a0001c0001t0001g0042 a0001c0001t0001g0043 |
2 | HG02145.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.154-12444G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148677770 | |||||||
| chr2:148677773 | C | T | 2 | a0001c0001t0001g0042 a0001c0001t0001g0043 |
2 | HG02145.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.154-12441C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148677773 | |||||||
| chr2:148677802 | C | T | 1 | a0001c0001t0002g0068 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.154-12412C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148677802 | |||||||
| chr2:148677831 | G | A | 3 | a0001c0001t0001g0036 a0001c0001t0001g0042 a0001c0001t0001g0043 |
3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.154-12383G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148677831 | |||||||
| chr2:148677892 | T | C | 2 | a0001c0001t0001g0034 a0001c0001t0001g0035 |
2 | NA19003.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.154-12322T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148677892 | |||||||
| chr2:148677896 | T | A | 1 | a0001c0001t0001g0306 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.154-12318T>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148677896 | |||||||
| chr2:148677927 | C | G | 1 | a0001c0001t0004g0177 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.154-12287C>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148677927 | |||||||
| chr2:148678013 | C | T | 9 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(6): Show |
9 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.154-12201C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148678013 | |||||||
| chr2:148678075 | T | C | 1 | a0001c0001t0001g0278 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.154-12139T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148678075 | |||||||
| chr2:148678079 | C | T | 1 | a0001c0001t0002g0102 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.154-12135C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148678079 | |||||||
| chr2:148678191 | A | C | 4 | a0001c0001t0001g0171 a0001c0001t0001g0241 a0001c0001t0001g0242 others(1): Show |
4 | HG00639.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.154-12023A>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148678191 | |||||||
| chr2:148678221 | G | C | 1 | a0001c0006t0001g0007 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.154-11993G>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148678221 | |||||||
| chr2:148678244 | A | G | 91 | a0001c0001t0002g0037 a0001c0001t0002g0038 a0001c0001t0002g0040 others(88): Show |
91 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.154-11970A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148678244 | |||||||
| chr2:148678277 | C | T | 1 | a0001c0001t0001g0028 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.154-11937C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148678277 | |||||||
| chr2:148678339 | C | G | 1 | a0001c0001t0001g0304 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.154-11875C>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148678339 | |||||||
| chr2:148678457 | G | A | 102 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0178 others(99): Show |
103 | HG00280.hp2 HG00423.hp2 HG00544.hp2 others(100): Show |
intron_variant | MODIFIER | c.154-11757G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148678457 | |||||||
| chr2:148678474 | G | A | 106 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(103): Show |
107 | HG00280.hp2 HG00423.hp2 HG00544.hp2 others(104): Show |
intron_variant | MODIFIER | c.154-11740G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148678474 | |||||||
| chr2:148678478 | T | G | 3 | a0001c0001t0001g0036 a0001c0001t0001g0042 a0001c0001t0001g0043 |
3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.154-11736T>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148678478 | |||||||
| chr2:148678481 | G | A | 3 | a0001c0001t0001g0036 a0001c0001t0001g0042 a0001c0001t0001g0043 |
3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.154-11733G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148678481 | |||||||
| chr2:148678533 | C | T | 1 | a0001c0001t0001g0145 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.154-11681C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148678533 | |||||||
| chr2:148678547 | C | A | 3 | a0001c0001t0001g0036 a0001c0001t0001g0042 a0001c0001t0001g0043 |
3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.154-11667C>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148678547 | |||||||
| chr2:148678641 | C | T | 10 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(7): Show |
10 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(7): Show |
intron_variant | MODIFIER | c.154-11573C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148678641 | |||||||
| chr2:148678757 | A | G | 119 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(116): Show |
120 | HG00280.hp2 HG00423.hp2 HG00544.hp2 others(117): Show |
intron_variant | MODIFIER | c.154-11457A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148678757 | |||||||
| chr2:148678838 | A | G | 2 | a0001c0001t0001g0281 a0001c0001t0001g0282 |
2 | HG02257.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.154-11376A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148678838 | |||||||
| chr2:148678848 | T | C | 12 | a0001c0001t0001g0171 a0001c0001t0001g0189 a0001c0001t0001g0190 others(9): Show |
12 | HG00639.hp1 HG02109.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.154-11366T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148678848 | |||||||
| chr2:148678860 | C | T | 4 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(1): Show |
4 | HG00639.hp2 HG02809.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.154-11354C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148678860 | |||||||
| chr2:148678894 | G | C | 91 | a0001c0001t0002g0037 a0001c0001t0002g0038 a0001c0001t0002g0040 others(88): Show |
91 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.154-11320G>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148678894 | |||||||
| chr2:148678902 | G | A | 3 | a0001c0001t0001g0036 a0001c0001t0001g0042 a0001c0001t0001g0043 |
3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.154-11312G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148678902 | |||||||
| chr2:148678941 | T | C | 1 | a0001c0001t0001g0149 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.154-11273T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148678941 | |||||||
| chr2:148679022 | C | T | 1 | a0001c0001t0001g0229 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.154-11192C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148679022 | |||||||
| chr2:148679557 | C | T | 2 | a0001c0001t0001g0292 a0001c0001t0001g0295 |
2 | NA18960.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.154-10657C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148679557 | |||||||
| chr2:148679719 | C | T | 1 | a0001c0001t0001g0263 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.154-10495C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148679719 | |||||||
| chr2:148679724 | C | T | 11 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0178 others(8): Show |
12 | HG00544.hp2 HG00609.hp2 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.154-10490C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148679724 | |||||||
| chr2:148679741 | G | A | 2 | a0001c0001t0001g0042 a0001c0001t0001g0043 |
2 | HG02145.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.154-10473G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148679741 | |||||||
| chr2:148679768 | C | G | 1 | a0001c0001t0001g0305 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.154-10446C>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148679768 | |||||||
| chr2:148679825 | T | A | 3 | a0001c0001t0001g0036 a0001c0001t0001g0042 a0001c0001t0001g0043 |
3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.154-10389T>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148679825 | |||||||
| chr2:148679833 | A | G | 6 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0191 others(3): Show |
6 | HG02109.hp2 HG02258.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.154-10381A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148679833 | |||||||
| chr2:148679886 | G | A | 5 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(2): Show |
5 | HG00639.hp2 HG02809.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.154-10328G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148679886 | |||||||
| chr2:148679938 | C | T | 1 | a0001c0001t0001g0012 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.154-10276C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148679938 | |||||||
| chr2:148680089 | C | CT | 26 | a0001c0001t0001g0188 a0001c0001t0001g0198 a0001c0001t0001g0199 others(23): Show |
26 | HG00280.hp2 HG00642.hp1 HG00642.hp2 others(23): Show |
intron_variant | MODIFIER | c.154-10110dupT | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148680089 | ||||||
| chr2:148680089 | CT | C | 16 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(13): Show |
16 | HG02040.hp2 HG02132.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.154-10110delT | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148680089 | ||||||
| chr2:148680090 | T | C | 6 | a0001c0001t0001g0171 a0001c0001t0001g0241 a0001c0001t0001g0242 others(3): Show |
6 | HG00639.hp1 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.154-10124T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148680090 | |||||||
| chr2:148680091 | T | C | 10 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0029 others(7): Show |
10 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(7): Show |
intron_variant | MODIFIER | c.154-10123T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148680091 | |||||||
| chr2:148680092 | T | C | 1 | a0001c0001t0001g0033 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.154-10122T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148680092 | |||||||
| chr2:148680280 | T | C | 3 | a0001c0001t0002g0063 a0001c0001t0002g0095 a0001c0001t0002g0096 |
3 | HG00673.hp1 HG02040.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.154-9934T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148680280 | |||||||
| chr2:148680534 | T | C | 3 | a0001c0001t0001g0036 a0001c0001t0001g0042 a0001c0001t0001g0043 |
3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.154-9680T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148680534 | |||||||
| chr2:148680623 | A | G | 1 | a0001c0001t0002g0087 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.154-9591A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148680623 | |||||||
| chr2:148680642 | G | A | 122 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(119): Show |
123 | HG00280.hp2 HG00423.hp2 HG00544.hp2 others(120): Show |
intron_variant | MODIFIER | c.154-9572G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148680642 | |||||||
| chr2:148680669 | G | A | 1 | a0001c0001t0003g0074 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.154-9545G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148680669 | |||||||
| chr2:148681006 | A | G | 3 | a0001c0001t0001g0036 a0001c0001t0001g0042 a0001c0001t0001g0043 |
3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.154-9208A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148681006 | |||||||
| chr2:148681039 | A | C | 20 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0001g0184 others(17): Show |
20 | HG00673.hp2 HG02074.hp2 HG04204.hp1 others(17): Show |
intron_variant | MODIFIER | c.154-9175A>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148681039 | |||||||
| chr2:148681271 | A | G | 1 | a0001c0001t0001g0131 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.154-8943A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148681271 | |||||||
| chr2:148681435 | T | C | 1 | a0001c0001t0001g0290 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.154-8779T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148681435 | |||||||
| chr2:148681624 | C | T | 119 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(116): Show |
120 | HG00280.hp2 HG00423.hp2 HG00544.hp2 others(117): Show |
intron_variant | MODIFIER | c.154-8590C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148681624 | |||||||
| chr2:148681625 | G | A | 1 | a0001c0001t0001g0144 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.154-8589G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148681625 | |||||||
| chr2:148681697 | GGTTT | G | 4 | a0001c0001t0001g0036 a0001c0001t0001g0042 a0001c0001t0001g0043 others(1): Show |
4 | HG02145.hp2 HG02895.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.154-8500_154-8497d others(6): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148681697 | ||||||
| chr2:148681714 | G | C | 2 | a0001c0001t0001g0193 a0001c0001t0002g0103 |
2 | HG02886.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.154-8500G>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148681714 | |||||||
| chr2:148681718 | C | G | 155 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(152): Show |
155 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(152): Show |
intron_variant | MODIFIER | c.154-8496C>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148681718 | |||||||
| chr2:148681756 | A | G | 11 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0178 others(8): Show |
12 | HG00544.hp2 HG00609.hp2 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.154-8458A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148681756 | |||||||
| chr2:148681821 | T | C | 2 | a0001c0001t0001g0198 a0001c0001t0001g0199 |
2 | HG02818.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.154-8393T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148681821 | |||||||
| chr2:148681868 | C | A | 1 | a0001c0001t0001g0195 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.154-8346C>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148681868 | |||||||
| chr2:148681891 | C | T | 1 | a0002c0002t0001g0253 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.154-8323C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148681891 | |||||||
| chr2:148681903 | G | A | 10 | a0001c0001t0001g0274 a0001c0001t0001g0275 a0001c0001t0001g0276 others(7): Show |
10 | HG02257.hp1 HG02257.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.154-8311G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148681903 | |||||||
| chr2:148681968 | G | A | 1 | a0001c0001t0001g0015 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.154-8246G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148681968 | |||||||
| chr2:148682027 | C | T | 10 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(7): Show |
10 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(7): Show |
intron_variant | MODIFIER | c.154-8187C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148682027 | |||||||
| chr2:148682070 | C | T | 1 | a0001c0001t0001g0260 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.154-8144C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148682070 | |||||||
| chr2:148682071 | G | A | 10 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(7): Show |
10 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(7): Show |
intron_variant | MODIFIER | c.154-8143G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148682071 | |||||||
| chr2:148682112 | A | G | 109 | a0001c0001t0001g0036 a0001c0001t0001g0042 a0001c0001t0001g0043 others(106): Show |
110 | HG00280.hp2 HG00423.hp2 HG00544.hp2 others(107): Show |
intron_variant | MODIFIER | c.154-8102A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148682112 | |||||||
| chr2:148682421 | C | G | 9 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(6): Show |
9 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.154-7793C>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148682421 | |||||||
| chr2:148682960 | A | T | 1 | a0001c0001t0001g0256 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.154-7254A>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148682960 | |||||||
| chr2:148683021 | C | T | 1 | a0001c0001t0002g0058 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.154-7193C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148683021 | |||||||
| chr2:148683081 | T | A | 102 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0178 others(99): Show |
103 | HG00280.hp2 HG00423.hp2 HG00544.hp2 others(100): Show |
intron_variant | MODIFIER | c.154-7133T>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148683081 | |||||||
| chr2:148683310 | C | T | 3 | a0001c0001t0001g0036 a0001c0001t0001g0042 a0001c0001t0001g0043 |
3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.154-6904C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148683310 | |||||||
| chr2:148683680 | A | G | 1 | a0001c0001t0001g0168 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.154-6534A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148683680 | |||||||
| chr2:148683725 | T | C | 1 | a0001c0001t0002g0090 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.154-6489T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148683725 | |||||||
| chr2:148683750 | T | C | 3 | a0001c0001t0001g0036 a0001c0001t0001g0042 a0001c0001t0001g0043 |
3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.154-6464T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148683750 | |||||||
| chr2:148683835 | T | G | 1 | a0001c0001t0001g0196 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.154-6379T>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148683835 | |||||||
| chr2:148683875 | G | T | 9 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(6): Show |
9 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.154-6339G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148683875 | |||||||
| chr2:148683906 | A | C | 1 | a0001c0001t0001g0306 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.154-6308A>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148683906 | |||||||
| chr2:148684035 | T | A | 1 | a0001c0001t0001g0267 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.154-6179T>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148684035 | |||||||
| chr2:148684096 | A | G | 1 | a0001c0001t0001g0279 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.154-6118A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148684096 | |||||||
| chr2:148684125 | T | C | 1 | a0001c0001t0001g0028 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.154-6089T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148684125 | |||||||
| chr2:148684282 | A | G | 5 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0191 others(2): Show |
5 | HG02258.hp1 HG02886.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.154-5932A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148684282 | |||||||
| chr2:148684581 | C | G | 4 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0165 others(1): Show |
4 | NA18939.hp2 NA18945.hp2 NA18956.hp1 others(1): Show |
intron_variant | MODIFIER | c.154-5633C>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148684581 | |||||||
| chr2:148684665 | G | A | 20 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0001g0184 others(17): Show |
20 | HG00673.hp2 HG02074.hp2 HG04204.hp1 others(17): Show |
intron_variant | MODIFIER | c.154-5549G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148684665 | |||||||
| chr2:148685250 | GT | G | 289 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(286): Show |
290 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(287): Show |
intron_variant | MODIFIER | c.154-4954delT | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148685250 | ||||||
| chr2:148685260 | T | G | 9 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(6): Show |
9 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.154-4954T>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148685260 | |||||||
| chr2:148685267 | T | C | 91 | a0001c0001t0002g0037 a0001c0001t0002g0038 a0001c0001t0002g0040 others(88): Show |
91 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.154-4947T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148685267 | |||||||
| chr2:148685301 | C | T | 91 | a0001c0001t0002g0037 a0001c0001t0002g0038 a0001c0001t0002g0040 others(88): Show |
91 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.154-4913C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148685301 | |||||||
| chr2:148685343 | A | G | 12 | a0001c0001t0001g0171 a0001c0001t0001g0189 a0001c0001t0001g0190 others(9): Show |
12 | HG00639.hp1 HG02109.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.154-4871A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148685343 | |||||||
| chr2:148685499 | G | A | 9 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(6): Show |
9 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.154-4715G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148685499 | |||||||
| chr2:148685557 | G | A | 3 | a0001c0001t0001g0036 a0001c0001t0001g0042 a0001c0001t0001g0043 |
3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.154-4657G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148685557 | |||||||
| chr2:148685624 | G | C | 1 | a0001c0001t0002g0124 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.154-4590G>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148685624 | |||||||
| chr2:148685654 | A | T | 8 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(5): Show |
8 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(5): Show |
intron_variant | MODIFIER | c.154-4560A>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148685654 | |||||||
| chr2:148685698 | C | T | 1 | a0001c0001t0002g0126 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.154-4516C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148685698 | |||||||
| chr2:148685724 | G | A | 20 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0001g0184 others(17): Show |
20 | HG00673.hp2 HG02074.hp2 HG04204.hp1 others(17): Show |
intron_variant | MODIFIER | c.154-4490G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148685724 | |||||||
| chr2:148685753 | T | C | 290 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(287): Show |
291 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(288): Show |
intron_variant | MODIFIER | c.154-4461T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148685753 | |||||||
| chr2:148685825 | A | G | 1 | a0001c0001t0001g0180 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.154-4389A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148685825 | |||||||
| chr2:148685991 | G | A | 1 | a0001c0001t0001g0170 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.154-4223G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148685991 | |||||||
| chr2:148686015 | G | A | 3 | a0001c0005t0001g0186 a0002c0002t0001g0307 a0002c0002t0006g0254 |
3 | HG02647.hp2 HG02965.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.154-4199G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148686015 | |||||||
| chr2:148686033 | A | G | 91 | a0001c0001t0002g0037 a0001c0001t0002g0038 a0001c0001t0002g0040 others(88): Show |
91 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.154-4181A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148686033 | |||||||
| chr2:148686450 | T | G | 3 | a0001c0001t0001g0036 a0001c0001t0001g0042 a0001c0001t0001g0043 |
3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.154-3764T>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148686450 | |||||||
| chr2:148686460 | G | A | 4 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0178 others(1): Show |
4 | HG03491.hp2 HG03492.hp1 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.154-3754G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148686460 | |||||||
| chr2:148687038 | C | T | 12 | a0001c0001t0001g0171 a0001c0001t0001g0189 a0001c0001t0001g0190 others(9): Show |
12 | HG00639.hp1 HG02109.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.154-3176C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148687038 | |||||||
| chr2:148687197 | A | G | 3 | a0001c0001t0001g0036 a0001c0001t0001g0042 a0001c0001t0001g0043 |
3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.154-3017A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148687197 | |||||||
| chr2:148687460 | T | G | 1 | a0001c0001t0001g0250 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.154-2754T>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148687460 | |||||||
| chr2:148687622 | C | A | 1 | a0001c0001t0001g0246 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.154-2592C>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148687622 | |||||||
| chr2:148687624 | A | G | 1 | a0001c0001t0001g0298 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.154-2590A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148687624 | |||||||
| chr2:148687794 | G | A | 1 | a0001c0001t0001g0004 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.154-2420G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148687794 | |||||||
| chr2:148687831 | C | T | 1 | a0001c0001t0001g0304 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.154-2383C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148687831 | |||||||
| chr2:148687906 | C | T | 91 | a0001c0001t0002g0037 a0001c0001t0002g0038 a0001c0001t0002g0040 others(88): Show |
91 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.154-2308C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148687906 | |||||||
| chr2:148688041 | TATA | T | 4 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(1): Show |
4 | HG00639.hp2 HG02809.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.154-2168_154-2166d others(5): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148688041 | ||||||
| chr2:148688086 | C | G | 1 | a0001c0001t0002g0086 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.154-2128C>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148688086 | |||||||
| chr2:148688302 | T | C | 2 | a0001c0001t0001g0023 a0001c0001t0001g0024 |
2 | HG02922.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.154-1912T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148688302 | |||||||
| chr2:148688419 | G | T | 1 | a0001c0001t0002g0068 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.154-1795G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148688419 | |||||||
| chr2:148688428 | G | A | 1 | a0001c0001t0001g0276 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.154-1786G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148688428 | |||||||
| chr2:148688459 | G | C | 4 | a0001c0001t0002g0099 a0001c0001t0002g0100 a0001c0001t0002g0101 others(1): Show |
4 | NA18947.hp1 NA18952.hp2 NA19064.hp2 others(1): Show |
intron_variant | MODIFIER | c.154-1755G>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148688459 | |||||||
| chr2:148688712 | T | C | 290 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(287): Show |
291 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(288): Show |
intron_variant | MODIFIER | c.154-1502T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148688712 | |||||||
| chr2:148688801 | G | A | 1 | a0001c0001t0001g0017 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.154-1413G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148688801 | |||||||
| chr2:148688959 | G | A | 5 | a0001c0001t0002g0115 a0001c0001t0002g0116 a0001c0001t0002g0117 others(2): Show |
5 | HG00423.hp2 HG02135.hp2 NA18956.hp2 others(2): Show |
intron_variant | MODIFIER | c.154-1255G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148688959 | |||||||
| chr2:148689035 | A | G | 1 | a0001c0001t0002g0111 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.154-1179A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148689035 | |||||||
| chr2:148689069 | G | T | 153 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0134 others(150): Show |
153 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(150): Show |
intron_variant | MODIFIER | c.154-1145G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148689069 | |||||||
| chr2:148689240 | G | T | 1 | a0001c0001t0001g0028 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.154-974G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148689240 | |||||||
| chr2:148689338 | G | A | 1 | a0001c0001t0001g0267 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.154-876G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148689338 | |||||||
| chr2:148689368 | C | T | 24 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0001g0184 others(21): Show |
24 | HG00673.hp2 HG02074.hp2 HG02647.hp2 others(21): Show |
intron_variant | MODIFIER | c.154-846C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148689368 | |||||||
| chr2:148689472 | A | C | 1 | a0001c0001t0001g0028 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.154-742A>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148689472 | |||||||
| chr2:148689893 | G | A | 11 | a0001c0001t0001g0028 a0001c0001t0001g0274 a0001c0001t0001g0275 others(8): Show |
11 | HG02257.hp1 HG02257.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.154-321G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148689893 | |||||||
| chr2:148689986 | T | TA | 112 | a0001c0001t0001g0036 a0001c0001t0001g0042 a0001c0001t0001g0043 others(109): Show |
113 | HG00280.hp2 HG00423.hp2 HG00544.hp2 others(110): Show |
intron_variant | MODIFIER | c.154-222dupA | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 148689986 | ||||||
| chr2:148689988 | A | AC | 10 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(7): Show |
10 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(7): Show |
intron_variant | MODIFIER | c.154-226_154-225ins others(1): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 1/13 | chr2 | 148689988 | |||||||
| chr2:148690410 | TA | T | 20 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0001g0184 others(17): Show |
20 | HG00673.hp2 HG02074.hp2 HG04204.hp1 others(17): Show |
intron_variant | MODIFIER | c.313+40delA | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148690410 | ||||||
| chr2:148690523 | G | T | 1 | a0001c0005t0001g0009 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.313+150G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148690523 | |||||||
| chr2:148690565 | A | T | 12 | a0001c0001t0001g0201 a0001c0001t0001g0213 a0001c0001t0001g0232 others(9): Show |
12 | HG00609.hp1 HG01346.hp2 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.313+192A>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148690565 | |||||||
| chr2:148690728 | T | C | 106 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(103): Show |
107 | HG00280.hp2 HG00423.hp2 HG00544.hp2 others(104): Show |
intron_variant | MODIFIER | c.313+355T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148690728 | |||||||
| chr2:148690729 | C | A | 4 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(1): Show |
4 | HG00639.hp2 HG02809.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.313+356C>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148690729 | |||||||
| chr2:148690734 | C | T | 1 | a0001c0001t0001g0033 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.313+361C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148690734 | |||||||
| chr2:148690963 | G | A | 24 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0001g0184 others(21): Show |
24 | HG00673.hp2 HG02074.hp2 HG02647.hp2 others(21): Show |
intron_variant | MODIFIER | c.313+590G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148690963 | |||||||
| chr2:148691077 | G | A | 4 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(1): Show |
4 | HG02145.hp1 HG02451.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.313+704G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148691077 | |||||||
| chr2:148691146 | G | A | 5 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0001c0003t0001g0249 others(2): Show |
5 | HG01884.hp1 HG02109.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.313+773G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148691146 | |||||||
| chr2:148691146 | G | T | 1 | a0001c0001t0001g0267 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.313+773G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148691146 | |||||||
| chr2:148691221 | C | T | 1 | a0002c0002t0006g0254 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.313+848C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148691221 | |||||||
| chr2:148691227 | A | T | 1 | a0001c0001t0001g0214 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.313+854A>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148691227 | |||||||
| chr2:148691300 | G | T | 3 | a0001c0001t0001g0232 a0001c0001t0001g0263 a0001c0001t0001g0264 |
3 | NA18612.hp2 NA18975.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.313+927G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148691300 | |||||||
| chr2:148691347 | G | A | 2 | a0001c0001t0001g0010 a0001c0001t0001g0029 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.313+974G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148691347 | |||||||
| chr2:148691401 | A | G | 1 | a0001c0001t0001g0218 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.313+1028A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148691401 | |||||||
| chr2:148691508 | T | C | 6 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0191 others(3): Show |
6 | HG02109.hp2 HG02258.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.313+1135T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148691508 | |||||||
| chr2:148691616 | G | A | 70 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0170 others(67): Show |
70 | HG00280.hp1 HG00609.hp1 HG00642.hp1 others(67): Show |
intron_variant | MODIFIER | c.313+1243G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148691616 | |||||||
| chr2:148691862 | C | T | 1 | a0001c0001t0001g0024 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.313+1489C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148691862 | |||||||
| chr2:148691980 | T | G | 1 | a0001c0001t0001g0238 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.313+1607T>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148691980 | |||||||
| chr2:148691999 | A | C | 1 | a0001c0001t0001g0273 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.313+1626A>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148691999 | |||||||
| chr2:148692156 | T | C | 1 | a0001c0001t0001g0279 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.313+1783T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148692156 | |||||||
| chr2:148692167 | A | G | 9 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(6): Show |
9 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.313+1794A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148692167 | |||||||
| chr2:148692282 | A | G | 10 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(7): Show |
10 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(7): Show |
intron_variant | MODIFIER | c.313+1909A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148692282 | |||||||
| chr2:148692624 | A | G | 3 | a0001c0001t0001g0036 a0001c0001t0001g0042 a0001c0001t0001g0043 |
3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.313+2251A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148692624 | |||||||
| chr2:148693148 | A | T | 6 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0001g0149 others(3): Show |
6 | HG00423.hp1 NA18981.hp2 NA19005.hp2 others(3): Show |
intron_variant | MODIFIER | c.313+2775A>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148693148 | |||||||
| chr2:148693157 | A | G | 2 | a0001c0001t0001g0042 a0001c0001t0001g0043 |
2 | HG02145.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.313+2784A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148693157 | |||||||
| chr2:148693272 | A | G | 4 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(1): Show |
4 | HG00639.hp2 HG02809.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.313+2899A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148693272 | |||||||
| chr2:148693295 | G | A | 1 | a0001c0001t0001g0225 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.313+2922G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148693295 | |||||||
| chr2:148693598 | C | T | 10 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(7): Show |
10 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(7): Show |
intron_variant | MODIFIER | c.313+3225C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148693598 | |||||||
| chr2:148693692 | C | G | 10 | a0001c0001t0001g0274 a0001c0001t0001g0275 a0001c0001t0001g0276 others(7): Show |
10 | HG02257.hp1 HG02257.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.313+3319C>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148693692 | |||||||
| chr2:148693908 | T | C | 8 | a0001c0001t0001g0140 a0001c0001t0001g0167 a0001c0001t0001g0283 others(5): Show |
8 | NA18747.hp1 NA18941.hp1 NA18947.hp2 others(5): Show |
intron_variant | MODIFIER | c.313+3535T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148693908 | |||||||
| chr2:148693910 | G | A | 4 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(1): Show |
4 | HG00639.hp2 HG02809.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.313+3537G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148693910 | |||||||
| chr2:148693916 | G | A | 4 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(1): Show |
4 | HG00639.hp2 HG02809.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.313+3543G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148693916 | |||||||
| chr2:148693993 | G | A | 102 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0178 others(99): Show |
103 | HG00280.hp2 HG00423.hp2 HG00544.hp2 others(100): Show |
intron_variant | MODIFIER | c.313+3620G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148693993 | |||||||
| chr2:148694020 | T | C | 106 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(103): Show |
107 | HG00280.hp2 HG00423.hp2 HG00544.hp2 others(104): Show |
intron_variant | MODIFIER | c.313+3647T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148694020 | |||||||
| chr2:148694224 | G | A | 3 | a0001c0001t0001g0036 a0001c0001t0001g0042 a0001c0001t0001g0043 |
3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.313+3851G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148694224 | |||||||
| chr2:148694270 | C | T | 2 | a0001c0001t0001g0174 a0001c0001t0001g0179 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.313+3897C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148694270 | |||||||
| chr2:148694304 | T | C | 1 | a0001c0001t0001g0195 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.313+3931T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148694304 | |||||||
| chr2:148694439 | T | C | 3 | a0001c0001t0001g0152 a0001c0001t0001g0161 a0001c0001t0001g0162 |
3 | HG01123.hp1 HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.313+4066T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148694439 | |||||||
| chr2:148694465 | A | G | 1 | a0001c0001t0002g0054 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.313+4092A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148694465 | |||||||
| chr2:148694626 | T | C | 2 | a0001c0001t0004g0173 a0001c0001t0004g0181 |
2 | HG00609.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.313+4253T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148694626 | |||||||
| chr2:148694709 | C | T | 4 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(1): Show |
4 | HG02145.hp1 HG02451.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.313+4336C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148694709 | |||||||
| chr2:148694769 | C | G | 2 | a0001c0001t0001g0258 a0001c0001t0001g0259 |
2 | HG00280.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.313+4396C>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148694769 | |||||||
| chr2:148694856 | C | T | 4 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(1): Show |
4 | HG00639.hp2 HG02809.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.313+4483C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148694856 | |||||||
| chr2:148695007 | A | G | 12 | a0001c0001t0001g0171 a0001c0001t0001g0189 a0001c0001t0001g0190 others(9): Show |
12 | HG00639.hp1 HG02109.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.313+4634A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148695007 | |||||||
| chr2:148695067 | C | T | 2 | a0001c0001t0001g0010 a0001c0001t0001g0029 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.313+4694C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148695067 | |||||||
| chr2:148695115 | C | A | 4 | a0001c0001t0002g0099 a0001c0001t0002g0100 a0001c0001t0002g0101 others(1): Show |
4 | NA18947.hp1 NA18952.hp2 NA19064.hp2 others(1): Show |
intron_variant | MODIFIER | c.313+4742C>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148695115 | |||||||
| chr2:148695160 | T | C | 4 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(1): Show |
4 | HG00639.hp2 HG02809.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.313+4787T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148695160 | |||||||
| chr2:148695231 | C | T | 1 | a0001c0001t0001g0304 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.313+4858C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148695231 | |||||||
| chr2:148695232 | G | A | 5 | a0001c0001t0001g0208 a0001c0001t0001g0219 a0001c0001t0001g0224 others(2): Show |
5 | HG00738.hp1 HG01070.hp1 HG01175.hp2 others(2): Show |
intron_variant | MODIFIER | c.313+4859G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148695232 | |||||||
| chr2:148695263 | G | C | 8 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(5): Show |
8 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(5): Show |
intron_variant | MODIFIER | c.313+4890G>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148695263 | |||||||
| chr2:148695727 | T | TA | 6 | a0001c0001t0002g0041 a0001c0001t0002g0071 a0001c0001t0002g0076 others(3): Show |
6 | HG02132.hp2 NA18946.hp2 NA18972.hp2 others(3): Show |
intron_variant | MODIFIER | c.313+5355dupA | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148695727 | ||||||
| chr2:148695786 | A | T | 1 | a0001c0001t0002g0069 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.313+5413A>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148695786 | |||||||
| chr2:148695896 | A | T | 3 | a0001c0001t0001g0036 a0001c0001t0001g0042 a0001c0001t0001g0043 |
3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.313+5523A>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148695896 | |||||||
| chr2:148695975 | C | A | 3 | a0001c0001t0001g0036 a0001c0001t0001g0042 a0001c0001t0001g0043 |
3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.313+5602C>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148695975 | |||||||
| chr2:148696159 | T | G | 3 | a0001c0001t0001g0036 a0001c0001t0001g0042 a0001c0001t0001g0043 |
3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.313+5786T>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148696159 | |||||||
| chr2:148696231 | T | G | 91 | a0001c0001t0002g0037 a0001c0001t0002g0038 a0001c0001t0002g0040 others(88): Show |
91 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.313+5858T>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148696231 | |||||||
| chr2:148696385 | G | A | 2 | a0001c0001t0001g0251 a0001c0001t0001g0252 |
2 | HG02572.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.313+6012G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148696385 | |||||||
| chr2:148696403 | C | A | 3 | a0001c0001t0001g0036 a0001c0001t0001g0042 a0001c0001t0001g0043 |
3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.313+6030C>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148696403 | |||||||
| chr2:148696647 | A | G | 126 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(123): Show |
127 | HG00280.hp2 HG00423.hp2 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.313+6274A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148696647 | |||||||
| chr2:148696652 | G | T | 3 | a0001c0001t0001g0036 a0001c0001t0001g0042 a0001c0001t0001g0043 |
3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.313+6279G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148696652 | |||||||
| chr2:148696676 | G | T | 2 | a0001c0001t0001g0131 a0001c0001t0001g0132 |
2 | HG02809.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.313+6303G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148696676 | |||||||
| chr2:148696731 | A | G | 102 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0178 others(99): Show |
103 | HG00280.hp2 HG00423.hp2 HG00544.hp2 others(100): Show |
intron_variant | MODIFIER | c.313+6358A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148696731 | |||||||
| chr2:148696737 | A | G | 1 | a0001c0001t0001g0306 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.313+6364A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148696737 | |||||||
| chr2:148696769 | C | T | 1 | a0001c0001t0001g0012 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.313+6396C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148696769 | |||||||
| chr2:148696842 | T | A | 1 | a0001c0001t0001g0306 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.313+6469T>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148696842 | |||||||
| chr2:148696891 | C | T | 2 | a0001c0001t0001g0206 a0001c0001t0001g0207 |
2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.313+6518C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148696891 | |||||||
| chr2:148697015 | T | C | 1 | a0001c0001t0001g0234 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.313+6642T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148697015 | |||||||
| chr2:148697016 | G | C | 1 | a0001c0001t0002g0111 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.313+6643G>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148697016 | |||||||
| chr2:148697038 | G | A | 290 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(287): Show |
291 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(288): Show |
intron_variant | MODIFIER | c.313+6665G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148697038 | |||||||
| chr2:148697127 | C | T | 1 | a0001c0001t0001g0130 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.313+6754C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148697127 | |||||||
| chr2:148697263 | A | G | 1 | a0001c0001t0002g0087 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.313+6890A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148697263 | |||||||
| chr2:148697327 | A | G | 2 | a0001c0001t0001g0144 a0001c0001t0001g0145 |
2 | HG00558.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.313+6954A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148697327 | |||||||
| chr2:148697399 | A | G | 4 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(1): Show |
4 | HG00639.hp2 HG02809.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.313+7026A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148697399 | |||||||
| chr2:148697498 | C | A | 1 | a0001c0001t0001g0194 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.313+7125C>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148697498 | |||||||
| chr2:148697612 | T | C | 1 | a0001c0001t0001g0250 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.313+7239T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148697612 | |||||||
| chr2:148697634 | A | G | 102 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0178 others(99): Show |
103 | HG00280.hp2 HG00423.hp2 HG00544.hp2 others(100): Show |
intron_variant | MODIFIER | c.313+7261A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148697634 | |||||||
| chr2:148697691 | A | G | 1 | a0001c0001t0001g0260 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.313+7318A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148697691 | |||||||
| chr2:148697727 | C | T | 4 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(1): Show |
4 | HG02145.hp1 HG02451.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.313+7354C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148697727 | |||||||
| chr2:148697816 | A | G | 106 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(103): Show |
107 | HG00280.hp2 HG00423.hp2 HG00544.hp2 others(104): Show |
intron_variant | MODIFIER | c.313+7443A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148697816 | |||||||
| chr2:148698047 | A | C | 3 | a0001c0001t0001g0250 a0001c0001t0001g0251 a0001c0001t0001g0252 |
3 | HG02572.hp2 HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.313+7674A>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148698047 | |||||||
| chr2:148698067 | T | A | 9 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(6): Show |
9 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.313+7694T>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148698067 | |||||||
| chr2:148698351 | G | C | 10 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(7): Show |
10 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(7): Show |
intron_variant | MODIFIER | c.313+7978G>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148698351 | |||||||
| chr2:148698364 | G | T | 2 | a0001c0004t0001g0013 a0001c0004t0001g0026 |
2 | HG01891.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.313+7991G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148698364 | |||||||
| chr2:148698370 | G | A | 9 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(6): Show |
9 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.313+7997G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148698370 | |||||||
| chr2:148698406 | G | A | 1 | a0001c0001t0002g0103 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.313+8033G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148698406 | |||||||
| chr2:148698452 | A | G | 111 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0134 others(108): Show |
111 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(108): Show |
intron_variant | MODIFIER | c.313+8079A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148698452 | |||||||
| chr2:148698465 | A | G | 12 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(9): Show |
12 | HG02040.hp2 HG02132.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.313+8092A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148698465 | |||||||
| chr2:148698467 | C | T | 91 | a0001c0001t0002g0037 a0001c0001t0002g0038 a0001c0001t0002g0040 others(88): Show |
91 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.313+8094C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148698467 | |||||||
| chr2:148698633 | C | CA | 20 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0022 others(17): Show |
20 | HG00423.hp1 HG00639.hp2 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.313+8285dupA | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148698633 | ||||||
| chr2:148698633 | C | CAA | 67 | a0001c0001t0001g0031 a0001c0001t0001g0035 a0001c0001t0001g0174 others(64): Show |
68 | HG00280.hp2 HG00544.hp2 HG00558.hp2 others(65): Show |
intron_variant | MODIFIER | c.313+8284_313+8285d others(4): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148698633 | ||||||
| chr2:148698633 | C | CAAA | 33 | a0001c0001t0001g0175 a0001c0001t0002g0038 a0001c0001t0002g0044 others(30): Show |
33 | HG00423.hp2 HG00673.hp1 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.313+8283_313+8285d others(5): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148698633 | ||||||
| chr2:148698633 | CA | C | 129 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(126): Show |
129 | HG00280.hp1 HG00544.hp1 HG00558.hp1 others(126): Show |
intron_variant | MODIFIER | c.313+8285delA | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148698633 | ||||||
| chr2:148698633 | CAAAAAAA others(6): Show |
C | 1 | a0001c0001t0001g0282 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.313+8273_313+8285d others(15): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148698633 | ||||||
| chr2:148698633 | CAAAAAAA others(7): Show |
C | 1 | a0001c0001t0001g0281 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.313+8272_313+8285d others(16): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148698633 | ||||||
| chr2:148698694 | C | CT | 76 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(73): Show |
76 | HG00609.hp1 HG00639.hp2 HG00642.hp1 others(73): Show |
intron_variant | MODIFIER | c.313+8339dupT | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148698694 | ||||||
| chr2:148698694 | C | CTT | 52 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(49): Show |
53 | HG00280.hp1 HG00544.hp2 HG00609.hp2 others(50): Show |
intron_variant | MODIFIER | c.313+8338_313+8339d others(4): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148698694 | ||||||
| chr2:148698694 | C | CTTT | 12 | a0001c0001t0001g0171 a0001c0001t0001g0241 a0001c0001t0001g0242 others(9): Show |
12 | HG00639.hp1 HG02027.hp1 HG02895.hp2 others(9): Show |
intron_variant | MODIFIER | c.313+8337_313+8339d others(5): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148698694 | ||||||
| chr2:148698694 | C | CTTTT | 72 | a0001c0001t0002g0037 a0001c0001t0002g0038 a0001c0001t0002g0041 others(69): Show |
72 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.313+8336_313+8339d others(6): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148698694 | ||||||
| chr2:148698694 | C | CTTTTT | 9 | a0001c0001t0002g0051 a0001c0001t0002g0059 a0001c0001t0002g0087 others(6): Show |
9 | HG00642.hp2 HG01175.hp1 HG02273.hp1 others(6): Show |
intron_variant | MODIFIER | c.313+8335_313+8339d others(7): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148698694 | ||||||
| chr2:148698694 | CT | C | 29 | a0001c0001t0001g0014 a0001c0001t0001g0036 a0001c0001t0001g0042 others(26): Show |
29 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(26): Show |
intron_variant | MODIFIER | c.313+8339delT | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148698694 | ||||||
| chr2:148698694 | CTT | C | 14 | a0001c0001t0001g0137 a0001c0001t0001g0140 a0001c0001t0001g0142 others(11): Show |
14 | HG02080.hp1 HG02135.hp1 NA18747.hp1 others(11): Show |
intron_variant | MODIFIER | c.313+8338_313+8339d others(4): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148698694 | ||||||
| chr2:148698829 | C | CT | 138 | a0001c0001t0001g0036 a0001c0001t0001g0042 a0001c0001t0001g0043 others(135): Show |
138 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(135): Show |
intron_variant | MODIFIER | c.313+8468dupT | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148698829 | ||||||
| chr2:148698829 | C | CTT | 108 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0129 others(105): Show |
109 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.313+8467_313+8468d others(4): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148698829 | ||||||
| chr2:148698829 | C | CTTT | 16 | a0001c0001t0001g0136 a0001c0001t0001g0141 a0001c0001t0001g0142 others(13): Show |
16 | HG00544.hp1 HG00558.hp1 HG02080.hp1 others(13): Show |
intron_variant | MODIFIER | c.313+8466_313+8468d others(5): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148698829 | ||||||
| chr2:148698841 | T | A | 1 | a0001c0001t0001g0304 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.313+8468T>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148698841 | |||||||
| chr2:148698841 | T | TA | 11 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(8): Show |
11 | HG00673.hp1 HG01884.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.313+8477dupA | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148698841 | ||||||
| chr2:148698842 | A | T | 15 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(12): Show |
15 | HG02040.hp2 HG02074.hp2 HG02132.hp1 others(12): Show |
intron_variant | MODIFIER | c.313+8469A>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148698842 | |||||||
| chr2:148698843 | A | T | 2 | a0001c0001t0001g0251 a0001c0001t0001g0252 |
2 | HG02572.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.313+8470A>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148698843 | |||||||
| chr2:148698859 | C | T | 1 | a0001c0001t0001g0168 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.313+8486C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148698859 | |||||||
| chr2:148698892 | G | A | 3 | a0001c0001t0001g0137 a0001c0001t0001g0158 a0001c0001t0001g0159 |
3 | NA18969.hp1 NA19001.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.313+8519G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148698892 | |||||||
| chr2:148698999 | C | A | 1 | a0001c0001t0002g0125 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.313+8626C>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148698999 | |||||||
| chr2:148699016 | C | G | 1 | a0001c0001t0001g0286 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.313+8643C>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148699016 | |||||||
| chr2:148699212 | A | G | 1 | a0001c0001t0003g0108 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.313+8839A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148699212 | |||||||
| chr2:148699692 | G | T | 3 | a0001c0001t0001g0036 a0001c0001t0001g0042 a0001c0001t0001g0043 |
3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.313+9319G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148699692 | |||||||
| chr2:148699813 | G | T | 107 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(104): Show |
107 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(104): Show |
intron_variant | MODIFIER | c.313+9440G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148699813 | |||||||
| chr2:148699816 | A | G | 1 | a0002c0002t0001g0253 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.313+9443A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148699816 | |||||||
| chr2:148699908 | T | C | 1 | a0001c0001t0002g0060 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.313+9535T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148699908 | |||||||
| chr2:148699963 | C | T | 1 | a0001c0001t0001g0215 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.313+9590C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148699963 | |||||||
| chr2:148700033 | G | C | 1 | a0001c0001t0001g0275 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.313+9660G>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148700033 | |||||||
| chr2:148700122 | C | T | 1 | a0001c0005t0001g0009 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.313+9749C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148700122 | |||||||
| chr2:148700123 | G | A | 107 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(104): Show |
107 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(104): Show |
intron_variant | MODIFIER | c.313+9750G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148700123 | |||||||
| chr2:148700169 | C | T | 3 | a0001c0001t0001g0250 a0001c0001t0001g0251 a0001c0001t0001g0252 |
3 | HG02572.hp2 HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.313+9796C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148700169 | |||||||
| chr2:148700406 | A | G | 121 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(118): Show |
122 | HG00280.hp2 HG00423.hp2 HG00544.hp2 others(119): Show |
intron_variant | MODIFIER | c.313+10033A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148700406 | |||||||
| chr2:148700464 | G | A | 3 | a0001c0001t0001g0036 a0001c0001t0001g0042 a0001c0001t0001g0043 |
3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.313+10091G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148700464 | |||||||
| chr2:148700479 | C | T | 1 | a0001c0001t0004g0173 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.313+10106C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148700479 | |||||||
| chr2:148700482 | C | T | 2 | a0001c0001t0001g0258 a0001c0001t0001g0259 |
2 | HG00280.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.313+10109C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148700482 | |||||||
| chr2:148700483 | C | G | 1 | a0001c0001t0001g0233 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.313+10110C>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148700483 | |||||||
| chr2:148700491 | C | G | 11 | a0001c0001t0002g0063 a0001c0001t0002g0079 a0001c0001t0002g0088 others(8): Show |
11 | HG00673.hp1 HG02040.hp1 HG02080.hp2 others(8): Show |
intron_variant | MODIFIER | c.313+10118C>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148700491 | |||||||
| chr2:148700494 | G | C | 1 | a0001c0001t0002g0067 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.313+10121G>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148700494 | |||||||
| chr2:148700499 | G | A | 1 | a0001c0001t0001g0160 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.313+10126G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148700499 | |||||||
| chr2:148700499 | G | T | 1 | a0001c0001t0002g0128 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.313+10126G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148700499 | |||||||
| chr2:148700690 | C | CT | 106 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(103): Show |
107 | HG00280.hp2 HG00423.hp2 HG00544.hp2 others(104): Show |
intron_variant | MODIFIER | c.313+10332dupT | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148700690 | ||||||
| chr2:148700690 | CT | C | 11 | a0001c0001t0001g0028 a0001c0001t0001g0228 a0001c0001t0001g0274 others(8): Show |
11 | HG01517.hp1 HG02257.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.313+10332delT | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148700690 | ||||||
| chr2:148700857 | A | C | 10 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(7): Show |
10 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(7): Show |
intron_variant | MODIFIER | c.313+10484A>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148700857 | |||||||
| chr2:148700906 | A | G | 287 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(284): Show |
288 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(285): Show |
intron_variant | MODIFIER | c.313+10533A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148700906 | |||||||
| chr2:148700956 | C | T | 1 | a0001c0001t0001g0304 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.313+10583C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148700956 | |||||||
| chr2:148700997 | G | A | 1 | a0001c0001t0001g0178 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.313+10624G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148700997 | |||||||
| chr2:148701135 | A | G | 5 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0001c0003t0001g0249 others(2): Show |
5 | HG01884.hp1 HG02109.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.313+10762A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148701135 | |||||||
| chr2:148701410 | T | C | 1 | a0001c0001t0002g0070 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.313+11037T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148701410 | |||||||
| chr2:148701470 | G | T | 1 | a0001c0001t0003g0108 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.313+11097G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148701470 | |||||||
| chr2:148701605 | T | C | 1 | a0001c0001t0002g0120 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.313+11232T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148701605 | |||||||
| chr2:148701678 | C | T | 1 | a0001c0001t0001g0155 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.313+11305C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148701678 | |||||||
| chr2:148701702 | A | G | 3 | a0001c0001t0001g0036 a0001c0001t0001g0042 a0001c0001t0001g0043 |
3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.313+11329A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148701702 | |||||||
| chr2:148701825 | T | C | 2 | a0001c0001t0001g0014 a0001c0001t0001g0027 |
2 | HG02717.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.313+11452T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148701825 | |||||||
| chr2:148701880 | T | G | 3 | a0001c0001t0001g0204 a0001c0001t0001g0205 a0001c0001t0001g0230 |
3 | HG01433.hp1 HG02004.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.313+11507T>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148701880 | |||||||
| chr2:148702008 | A | G | 1 | a0001c0001t0001g0226 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.313+11635A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148702008 | |||||||
| chr2:148702067 | T | A | 1 | a0001c0001t0001g0224 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.313+11694T>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148702067 | |||||||
| chr2:148702698 | G | A | 20 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0001g0184 others(17): Show |
20 | HG00673.hp2 HG02074.hp2 HG04204.hp1 others(17): Show |
intron_variant | MODIFIER | c.313+12325G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148702698 | |||||||
| chr2:148702723 | A | G | 11 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0178 others(8): Show |
12 | HG00544.hp2 HG00609.hp2 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.313+12350A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148702723 | |||||||
| chr2:148702823 | AT | A | 105 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(102): Show |
105 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(102): Show |
intron_variant | MODIFIER | c.313+12462delT | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148702823 | ||||||
| chr2:148702839 | A | AT | 10 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(7): Show |
10 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(7): Show |
intron_variant | MODIFIER | c.313+12472dupT | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148702839 | ||||||
| chr2:148702979 | C | A | 4 | a0001c0001t0001g0171 a0001c0001t0001g0241 a0001c0001t0001g0242 others(1): Show |
4 | HG00639.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.313+12606C>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148702979 | |||||||
| chr2:148703185 | T | C | 1 | a0001c0001t0001g0275 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.313+12812T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148703185 | |||||||
| chr2:148703254 | A | C | 10 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(7): Show |
10 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(7): Show |
intron_variant | MODIFIER | c.313+12881A>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148703254 | |||||||
| chr2:148703442 | GT | G | 276 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(273): Show |
277 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(274): Show |
intron_variant | MODIFIER | c.313+13078delT | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148703442 | ||||||
| chr2:148703961 | A | C | 1 | a0001c0005t0001g0009 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.313+13588A>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148703961 | |||||||
| chr2:148703966 | G | C | 3 | a0001c0001t0001g0036 a0001c0001t0001g0042 a0001c0001t0001g0043 |
3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.313+13593G>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148703966 | |||||||
| chr2:148704110 | G | A | 91 | a0001c0001t0002g0037 a0001c0001t0002g0038 a0001c0001t0002g0040 others(88): Show |
91 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.313+13737G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148704110 | |||||||
| chr2:148704186 | G | C | 9 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(6): Show |
9 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.313+13813G>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148704186 | |||||||
| chr2:148704258 | C | T | 301 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(298): Show |
302 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(299): Show |
intron_variant | MODIFIER | c.313+13885C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148704258 | |||||||
| chr2:148704333 | G | T | 91 | a0001c0001t0002g0037 a0001c0001t0002g0038 a0001c0001t0002g0040 others(88): Show |
91 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.313+13960G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148704333 | |||||||
| chr2:148704369 | T | G | 2 | a0001c0001t0001g0251 a0001c0001t0001g0252 |
2 | HG02572.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.313+13996T>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148704369 | |||||||
| chr2:148704452 | A | G | 2 | a0001c0001t0001g0281 a0001c0001t0001g0282 |
2 | HG02257.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.313+14079A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148704452 | |||||||
| chr2:148704579 | A | G | 2 | a0001c0001t0001g0206 a0001c0001t0001g0207 |
2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.313+14206A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148704579 | |||||||
| chr2:148704965 | T | C | 3 | a0001c0001t0002g0059 a0001c0001t0002g0111 a0001c0001t0002g0133 |
3 | HG00741.hp1 HG01496.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.313+14592T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148704965 | |||||||
| chr2:148705220 | C | G | 1 | a0001c0001t0001g0215 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.313+14847C>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148705220 | |||||||
| chr2:148705297 | TA | T | 107 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(104): Show |
107 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(104): Show |
intron_variant | MODIFIER | c.313+14934delA | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148705297 | ||||||
| chr2:148705415 | C | T | 5 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0001c0003t0001g0249 others(2): Show |
5 | HG01884.hp1 HG02109.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.313+15042C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148705415 | |||||||
| chr2:148705611 | CT | C | 5 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0001c0003t0001g0249 others(2): Show |
5 | HG01884.hp1 HG02109.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.313+15239delT | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148705611 | |||||||
| chr2:148705691 | G | T | 3 | a0001c0001t0001g0250 a0001c0001t0001g0251 a0001c0001t0001g0252 |
3 | HG02572.hp2 HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.313+15318G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148705691 | |||||||
| chr2:148705707 | C | CAG | 10 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(7): Show |
10 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(7): Show |
intron_variant | MODIFIER | c.313+15334_313+1533 others(6): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148705707 | |||||||
| chr2:148705754 | G | A | 4 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(1): Show |
4 | HG00639.hp2 HG02809.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.313+15381G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148705754 | |||||||
| chr2:148705874 | A | G | 1 | a0001c0001t0001g0167 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.313+15501A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148705874 | |||||||
| chr2:148705888 | G | T | 2 | a0001c0001t0001g0258 a0001c0001t0001g0259 |
2 | HG00280.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.313+15515G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148705888 | |||||||
| chr2:148705933 | C | T | 10 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(7): Show |
10 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(7): Show |
intron_variant | MODIFIER | c.313+15560C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148705933 | |||||||
| chr2:148705974 | C | T | 2 | a0001c0001t0001g0268 a0001c0001t0001g0282 |
2 | HG02257.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.313+15601C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148705974 | |||||||
| chr2:148705975 | G | A | 15 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0178 others(12): Show |
16 | HG00544.hp2 HG00609.hp2 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.313+15602G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148705975 | |||||||
| chr2:148705990 | G | A | 1 | a0001c0001t0001g0156 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.313+15617G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148705990 | |||||||
| chr2:148706035 | G | A | 2 | a0001c0004t0001g0013 a0001c0004t0001g0026 |
2 | HG01891.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.313+15662G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148706035 | |||||||
| chr2:148706222 | C | T | 2 | a0001c0001t0001g0200 a0001c0001t0001g0266 |
2 | HG02015.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.313+15849C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148706222 | |||||||
| chr2:148706425 | A | G | 1 | a0001c0001t0001g0260 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.313+16052A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148706425 | |||||||
| chr2:148706513 | A | G | 1 | a0001c0001t0001g0234 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.313+16140A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148706513 | |||||||
| chr2:148706515 | C | T | 4 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(1): Show |
4 | HG00639.hp2 HG02809.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.313+16142C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148706515 | |||||||
| chr2:148706664 | C | G | 1 | a0001c0001t0002g0122 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.313+16291C>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148706664 | |||||||
| chr2:148706745 | C | G | 1 | a0001c0001t0001g0304 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.313+16372C>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148706745 | |||||||
| chr2:148706756 | A | C | 1 | a0001c0001t0002g0120 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.313+16383A>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148706756 | |||||||
| chr2:148706783 | A | C | 1 | a0001c0001t0002g0058 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.313+16410A>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148706783 | |||||||
| chr2:148706784 | G | A | 1 | a0001c0001t0001g0004 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.313+16411G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148706784 | |||||||
| chr2:148706809 | G | A | 1 | a0001c0001t0001g0250 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.313+16436G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148706809 | |||||||
| chr2:148706827 | G | A | 3 | a0001c0001t0001g0036 a0001c0001t0001g0042 a0001c0001t0001g0043 |
3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.313+16454G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148706827 | |||||||
| chr2:148706962 | A | G | 3 | a0001c0001t0001g0212 a0001c0001t0001g0227 a0001c0001t0001g0247 |
3 | NA18954.hp1 NA18970.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.313+16589A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148706962 | |||||||
| chr2:148707087 | T | C | 1 | a0001c0001t0001g0031 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.313+16714T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148707087 | |||||||
| chr2:148707250 | A | G | 9 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(6): Show |
9 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.313+16877A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148707250 | |||||||
| chr2:148707251 | A | C | 1 | a0001c0001t0001g0242 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.313+16878A>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148707251 | |||||||
| chr2:148707390 | A | T | 1 | a0001c0001t0001g0240 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.313+17017A>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148707390 | |||||||
| chr2:148707435 | T | C | 1 | a0001c0001t0001g0166 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.313+17062T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148707435 | |||||||
| chr2:148707459 | G | T | 3 | a0001c0001t0001g0036 a0001c0001t0001g0042 a0001c0001t0001g0043 |
3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.313+17086G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148707459 | |||||||
| chr2:148707572 | T | C | 4 | a0001c0001t0001g0171 a0001c0001t0001g0241 a0001c0001t0001g0242 others(1): Show |
4 | HG00639.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.313+17199T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148707572 | |||||||
| chr2:148707613 | G | A | 9 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(6): Show |
9 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.313+17240G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148707613 | |||||||
| chr2:148707622 | A | C | 3 | a0001c0001t0001g0036 a0001c0001t0001g0042 a0001c0001t0001g0043 |
3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.313+17249A>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148707622 | |||||||
| chr2:148707691 | A | G | 3 | a0001c0001t0001g0250 a0001c0001t0001g0251 a0001c0001t0001g0252 |
3 | HG02572.hp2 HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.313+17318A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148707691 | |||||||
| chr2:148707878 | A | G | 9 | a0001c0001t0002g0040 a0001c0001t0002g0075 a0001c0001t0002g0080 others(6): Show |
9 | HG02071.hp2 NA18950.hp2 NA18970.hp1 others(6): Show |
intron_variant | MODIFIER | c.313+17505A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148707878 | |||||||
| chr2:148707915 | C | A | 1 | a0001c0001t0007g0217 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.313+17542C>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148707915 | |||||||
| chr2:148707986 | ATAACT | A | 4 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(1): Show |
4 | HG00639.hp2 HG02809.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.313+17617_313+1762 others(9): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148707986 | ||||||
| chr2:148708097 | G | A | 1 | a0001c0001t0001g0135 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.313+17724G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148708097 | |||||||
| chr2:148708308 | G | C | 3 | a0001c0001t0001g0036 a0001c0001t0001g0042 a0001c0001t0001g0043 |
3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.313+17935G>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148708308 | |||||||
| chr2:148708415 | A | G | 1 | a0001c0001t0001g0043 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.313+18042A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148708415 | |||||||
| chr2:148708458 | A | C | 106 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(103): Show |
107 | HG00280.hp2 HG00423.hp2 HG00544.hp2 others(104): Show |
intron_variant | MODIFIER | c.313+18085A>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148708458 | |||||||
| chr2:148708527 | C | T | 4 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(1): Show |
4 | HG00639.hp2 HG02809.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.313+18154C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148708527 | |||||||
| chr2:148708531 | GAC | G | 4 | a0001c0005t0001g0186 a0002c0002t0001g0253 a0002c0002t0001g0307 others(1): Show |
4 | HG02647.hp2 HG02965.hp1 NA20300.hp1 others(1): Show |
intron_variant | MODIFIER | c.313+18162_313+1816 others(6): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148708531 | ||||||
| chr2:148708577 | T | C | 2 | a0001c0001t0001g0187 a0001c0001t0001g0248 |
2 | HG02717.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.313+18204T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148708577 | |||||||
| chr2:148708647 | A | G | 1 | a0001c0001t0007g0217 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.313+18274A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148708647 | |||||||
| chr2:148708747 | G | A | 107 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(104): Show |
107 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(104): Show |
intron_variant | MODIFIER | c.313+18374G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148708747 | |||||||
| chr2:148708861 | A | G | 3 | a0001c0001t0001g0036 a0001c0001t0001g0042 a0001c0001t0001g0043 |
3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.313+18488A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148708861 | |||||||
| chr2:148708955 | C | T | 3 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0229 |
3 | HG01175.hp2 HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.313+18582C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148708955 | |||||||
| chr2:148709028 | C | T | 121 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(118): Show |
122 | HG00280.hp2 HG00423.hp2 HG00544.hp2 others(119): Show |
intron_variant | MODIFIER | c.313+18655C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148709028 | |||||||
| chr2:148709031 | A | G | 1 | a0001c0001t0002g0060 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.313+18658A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148709031 | |||||||
| chr2:148709333 | C | T | 11 | a0001c0001t0001g0178 a0001c0001t0001g0274 a0001c0001t0001g0275 others(8): Show |
11 | HG02257.hp1 HG02257.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.313+18960C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148709333 | |||||||
| chr2:148709371 | C | T | 1 | a0001c0001t0001g0215 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.313+18998C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148709371 | |||||||
| chr2:148709444 | C | T | 3 | a0001c0001t0001g0036 a0001c0001t0001g0042 a0001c0001t0001g0043 |
3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.313+19071C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148709444 | |||||||
| chr2:148709446 | T | A | 3 | a0001c0001t0001g0171 a0001c0001t0001g0241 a0001c0001t0001g0243 |
3 | HG02895.hp2 HG02897.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.313+19073T>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148709446 | |||||||
| chr2:148709447 | C | G | 1 | a0001c0001t0001g0006 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.313+19074C>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148709447 | |||||||
| chr2:148709459 | A | G | 2 | a0001c0001t0001g0188 a0001c0001t0001g0228 |
2 | HG00642.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.313+19086A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148709459 | |||||||
| chr2:148709505 | A | G | 8 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(5): Show |
8 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(5): Show |
intron_variant | MODIFIER | c.313+19132A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148709505 | |||||||
| chr2:148709672 | A | G | 9 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(6): Show |
9 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.313+19299A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148709672 | |||||||
| chr2:148709931 | G | T | 1 | a0001c0001t0001g0156 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.313+19558G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148709931 | |||||||
| chr2:148709944 | A | C | 2 | a0001c0001t0001g0236 a0001c0001t0001g0237 |
2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.313+19571A>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148709944 | |||||||
| chr2:148709976 | A | C | 1 | a0001c0001t0001g0134 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.313+19603A>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148709976 | |||||||
| chr2:148709978 | A | G | 2 | a0001c0001t0001g0042 a0001c0001t0001g0043 |
2 | HG02145.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.313+19605A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148709978 | |||||||
| chr2:148710002 | C | G | 1 | a0001c0001t0002g0063 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.313+19629C>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148710002 | |||||||
| chr2:148710004 | A | G | 4 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(1): Show |
4 | HG00639.hp2 HG02809.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.313+19631A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148710004 | |||||||
| chr2:148710006 | TTAAAC | T | 9 | a0001c0001t0002g0038 a0001c0001t0002g0053 a0001c0001t0002g0054 others(6): Show |
9 | HG00280.hp2 HG00741.hp2 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.313+19638_313+1964 others(9): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148710006 | ||||||
| chr2:148710062 | CCTACAGA others(21): Show |
C | 1 | a0001c0001t0001g0240 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.313+19694_313+1972 others(32): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148710062 | ||||||
| chr2:148710226 | C | T | 1 | a0001c0001t0001g0267 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.313+19853C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148710226 | |||||||
| chr2:148710327 | G | A | 1 | a0001c0001t0001g0250 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.313+19954G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148710327 | |||||||
| chr2:148710338 | G | T | 9 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(6): Show |
9 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.313+19965G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148710338 | |||||||
| chr2:148710397 | G | T | 6 | a0001c0001t0003g0062 a0001c0001t0003g0074 a0001c0001t0003g0084 others(3): Show |
6 | HG00558.hp2 HG01981.hp2 HG02004.hp2 others(3): Show |
intron_variant | MODIFIER | c.313+20024G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148710397 | |||||||
| chr2:148710398 | G | T | 6 | a0001c0001t0003g0062 a0001c0001t0003g0074 a0001c0001t0003g0084 others(3): Show |
6 | HG00558.hp2 HG01981.hp2 HG02004.hp2 others(3): Show |
intron_variant | MODIFIER | c.313+20025G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148710398 | |||||||
| chr2:148710458 | A | G | 11 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0178 others(8): Show |
12 | HG00544.hp2 HG00609.hp2 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.313+20085A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148710458 | |||||||
| chr2:148710553 | T | C | 3 | a0001c0001t0002g0088 a0001c0001t0002g0089 a0001c0001t0002g0091 |
3 | NA18975.hp1 NA19077.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.313+20180T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148710553 | |||||||
| chr2:148710576 | G | A | 118 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(115): Show |
119 | HG00280.hp2 HG00423.hp2 HG00544.hp2 others(116): Show |
intron_variant | MODIFIER | c.313+20203G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148710576 | |||||||
| chr2:148710683 | T | TC | 118 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(115): Show |
119 | HG00280.hp2 HG00423.hp2 HG00544.hp2 others(116): Show |
intron_variant | MODIFIER | c.313+20310_313+2031 others(5): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148710683 | |||||||
| chr2:148710728 | C | T | 1 | a0001c0001t0001g0290 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.313+20355C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148710728 | |||||||
| chr2:148710762 | C | T | 13 | a0001c0001t0001g0043 a0001c0001t0001g0171 a0001c0001t0001g0189 others(10): Show |
13 | HG00639.hp1 HG02109.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.313+20389C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148710762 | |||||||
| chr2:148710852 | G | T | 2 | a0001c0001t0001g0233 a0001c0001t0001g0257 |
2 | HG01515.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.313+20479G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148710852 | |||||||
| chr2:148710880 | A | G | 1 | a0001c0001t0001g0276 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.313+20507A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148710880 | |||||||
| chr2:148710968 | A | G | 11 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0178 others(8): Show |
12 | HG00544.hp2 HG00609.hp2 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.313+20595A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148710968 | |||||||
| chr2:148710996 | T | C | 1 | a0001c0001t0001g0215 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.313+20623T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148710996 | |||||||
| chr2:148711029 | C | CTT | 3 | a0001c0001t0001g0036 a0001c0001t0001g0042 a0001c0001t0001g0043 |
3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.313+20660_313+2066 others(6): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148711029 | ||||||
| chr2:148711127 | T | A | 1 | a0001c0001t0002g0038 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.313+20754T>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148711127 | |||||||
| chr2:148711231 | G | A | 3 | a0001c0001t0001g0036 a0001c0001t0001g0042 a0001c0001t0001g0043 |
3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.313+20858G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148711231 | |||||||
| chr2:148711374 | T | C | 2 | a0001c0001t0001g0251 a0001c0001t0001g0252 |
2 | HG02572.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.313+21001T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148711374 | |||||||
| chr2:148711438 | C | G | 1 | a0001c0001t0002g0096 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.313+21065C>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148711438 | |||||||
| chr2:148711467 | C | T | 9 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(6): Show |
9 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.313+21094C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148711467 | |||||||
| chr2:148711750 | ATAGT | A | 4 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0202 others(1): Show |
4 | NA18985.hp2 NA19006.hp1 NA19077.hp1 others(1): Show |
intron_variant | MODIFIER | c.313+21379_313+2138 others(8): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148711750 | ||||||
| chr2:148711777 | A | C | 3 | a0001c0001t0001g0036 a0001c0001t0001g0042 a0001c0001t0001g0043 |
3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.313+21404A>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148711777 | |||||||
| chr2:148711823 | T | G | 1 | a0001c0001t0002g0083 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.313+21450T>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148711823 | |||||||
| chr2:148711842 | T | C | 106 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(103): Show |
107 | HG00280.hp2 HG00423.hp2 HG00544.hp2 others(104): Show |
intron_variant | MODIFIER | c.313+21469T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148711842 | |||||||
| chr2:148712144 | G | A | 111 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0134 others(108): Show |
111 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(108): Show |
intron_variant | MODIFIER | c.313+21771G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148712144 | |||||||
| chr2:148712242 | G | GGT | 5 | a0001c0001t0001g0250 a0001c0001t0001g0251 a0001c0001t0001g0252 others(2): Show |
5 | HG01943.hp1 HG02572.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.313+21870_313+2187 others(6): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148712242 | ||||||
| chr2:148712244 | G | T | 109 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(106): Show |
109 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(106): Show |
intron_variant | MODIFIER | c.313+21871G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148712244 | |||||||
| chr2:148712392 | G | GT | 4 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(1): Show |
4 | HG00639.hp2 HG02809.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.313+22020dupT | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148712392 | ||||||
| chr2:148712445 | A | G | 9 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(6): Show |
9 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.313+22072A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148712445 | |||||||
| chr2:148712577 | T | C | 2 | a0001c0001t0001g0131 a0001c0001t0001g0132 |
2 | HG02809.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.313+22204T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148712577 | |||||||
| chr2:148712660 | C | CTGGAAGA others(1): Show |
11 | a0001c0001t0001g0028 a0001c0001t0001g0274 a0001c0001t0001g0275 others(8): Show |
11 | HG02257.hp1 HG02257.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.313+22290_313+2229 others(12): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148712660 | ||||||
| chr2:148712682 | G | A | 1 | a0001c0001t0001g0178 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.313+22309G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148712682 | |||||||
| chr2:148712712 | G | C | 8 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(5): Show |
8 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(5): Show |
intron_variant | MODIFIER | c.313+22339G>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148712712 | |||||||
| chr2:148712753 | T | C | 10 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0015 others(7): Show |
10 | HG01891.hp1 HG02258.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.313+22380T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148712753 | |||||||
| chr2:148712835 | A | C | 1 | a0001c0001t0001g0132 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.313+22462A>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148712835 | |||||||
| chr2:148712937 | C | T | 1 | a0001c0006t0001g0007 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.313+22564C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148712937 | |||||||
| chr2:148712963 | C | T | 91 | a0001c0001t0002g0037 a0001c0001t0002g0038 a0001c0001t0002g0040 others(88): Show |
91 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.313+22590C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148712963 | |||||||
| chr2:148713007 | A | G | 1 | a0001c0001t0001g0136 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.313+22634A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148713007 | |||||||
| chr2:148713098 | A | G | 1 | a0001c0001t0001g0279 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.313+22725A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148713098 | |||||||
| chr2:148713145 | T | C | 4 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(1): Show |
4 | HG00639.hp2 HG02809.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.313+22772T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148713145 | |||||||
| chr2:148713314 | C | G | 4 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(1): Show |
4 | HG00639.hp2 HG02809.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.313+22941C>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148713314 | |||||||
| chr2:148713316 | A | G | 1 | a0001c0001t0001g0306 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.313+22943A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148713316 | |||||||
| chr2:148713462 | TAA | T | 4 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(1): Show |
4 | HG00639.hp2 HG02809.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.313+23092_313+2309 others(6): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148713462 | ||||||
| chr2:148713518 | A | T | 1 | a0001c0001t0001g0275 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.313+23145A>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148713518 | |||||||
| chr2:148713519 | T | A | 8 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(5): Show |
8 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(5): Show |
intron_variant | MODIFIER | c.313+23146T>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148713519 | |||||||
| chr2:148713630 | A | G | 1 | a0001c0001t0002g0122 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.313+23257A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148713630 | |||||||
| chr2:148713678 | A | G | 95 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(92): Show |
95 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.313+23305A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148713678 | |||||||
| chr2:148713682 | T | C | 1 | a0001c0001t0002g0087 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.313+23309T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148713682 | |||||||
| chr2:148713798 | C | T | 1 | a0001c0001t0001g0239 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.313+23425C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148713798 | |||||||
| chr2:148714092 | G | C | 4 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(1): Show |
4 | HG00639.hp2 HG02809.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.313+23719G>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148714092 | |||||||
| chr2:148714433 | G | T | 107 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(104): Show |
107 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(104): Show |
intron_variant | MODIFIER | c.313+24060G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148714433 | |||||||
| chr2:148714445 | G | GTCAAAT | 4 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0001g0184 others(1): Show |
4 | NA18954.hp2 NA19001.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.313+24073_313+2407 others(10): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148714445 | ||||||
| chr2:148714558 | A | T | 3 | a0001c0001t0001g0036 a0001c0001t0001g0042 a0001c0001t0001g0043 |
3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.313+24185A>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148714558 | |||||||
| chr2:148714772 | A | G | 20 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0001g0184 others(17): Show |
20 | HG00673.hp2 HG02074.hp2 HG04204.hp1 others(17): Show |
intron_variant | MODIFIER | c.313+24399A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148714772 | |||||||
| chr2:148714801 | A | G | 3 | a0001c0001t0001g0250 a0001c0001t0001g0251 a0001c0001t0001g0252 |
3 | HG02572.hp2 HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.313+24428A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148714801 | |||||||
| chr2:148714861 | T | C | 95 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(92): Show |
95 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.313+24488T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148714861 | |||||||
| chr2:148715025 | G | GT | 10 | a0001c0001t0001g0005 a0001c0001t0001g0017 a0001c0001t0001g0022 others(7): Show |
10 | HG01891.hp1 HG02132.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.313+24677dupT | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148715025 | ||||||
| chr2:148715025 | GT | G | 124 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0134 others(121): Show |
125 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(122): Show |
intron_variant | MODIFIER | c.313+24677delT | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148715025 | ||||||
| chr2:148715025 | GTT | G | 13 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0246 others(10): Show |
13 | HG00673.hp2 HG04184.hp2 NA18954.hp2 others(10): Show |
intron_variant | MODIFIER | c.313+24676_313+2467 others(6): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148715025 | ||||||
| chr2:148715025 | GTTTTTTT others(4): Show |
G | 3 | a0001c0001t0002g0085 a0001c0001t0002g0093 a0001c0001t0002g0127 |
3 | HG02071.hp2 HG02602.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.313+24667_313+2467 others(15): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148715025 | ||||||
| chr2:148715025 | GTTTTTTT others(5): Show |
G | 92 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(89): Show |
92 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(89): Show |
intron_variant | MODIFIER | c.313+24666_313+2467 others(16): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148715025 | ||||||
| chr2:148715191 | A | G | 110 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(107): Show |
110 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(107): Show |
intron_variant | MODIFIER | c.313+24818A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148715191 | |||||||
| chr2:148715324 | C | T | 2 | a0001c0001t0001g0171 a0001c0001t0001g0241 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.313+24951C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148715324 | |||||||
| chr2:148715341 | C | T | 1 | a0001c0001t0001g0134 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.313+24968C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148715341 | |||||||
| chr2:148715342 | G | A | 19 | a0001c0001t0002g0038 a0001c0001t0002g0053 a0001c0001t0002g0054 others(16): Show |
19 | HG00280.hp2 HG00642.hp2 HG00735.hp1 others(16): Show |
intron_variant | MODIFIER | c.313+24969G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148715342 | |||||||
| chr2:148715577 | G | A | 1 | a0001c0001t0001g0198 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.313+25204G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148715577 | |||||||
| chr2:148715604 | T | C | 8 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(5): Show |
8 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(5): Show |
intron_variant | MODIFIER | c.313+25231T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148715604 | |||||||
| chr2:148715687 | G | A | 5 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0178 others(2): Show |
5 | HG01106.hp2 HG03491.hp2 HG03492.hp1 others(2): Show |
intron_variant | MODIFIER | c.313+25314G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148715687 | |||||||
| chr2:148716064 | C | T | 1 | a0001c0001t0001g0201 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.313+25691C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148716064 | |||||||
| chr2:148716130 | G | A | 1 | a0001c0001t0001g0227 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.313+25757G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148716130 | |||||||
| chr2:148716379 | A | C | 290 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(287): Show |
291 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(288): Show |
intron_variant | MODIFIER | c.313+26006A>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148716379 | |||||||
| chr2:148716609 | G | A | 4 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(1): Show |
4 | HG00639.hp2 HG02809.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.313+26236G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148716609 | |||||||
| chr2:148716669 | C | T | 3 | a0001c0001t0001g0232 a0001c0001t0001g0263 a0001c0001t0001g0264 |
3 | NA18612.hp2 NA18975.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.313+26296C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148716669 | |||||||
| chr2:148716728 | T | G | 1 | a0001c0001t0002g0060 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.313+26355T>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148716728 | |||||||
| chr2:148716872 | G | C | 1 | a0001c0001t0001g0224 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.313+26499G>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148716872 | |||||||
| chr2:148716903 | G | A | 1 | a0001c0001t0001g0200 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.313+26530G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148716903 | |||||||
| chr2:148717074 | G | A | 1 | a0001c0001t0001g0226 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.314-26548G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148717074 | |||||||
| chr2:148717193 | A | AT | 7 | a0001c0001t0001g0042 a0001c0001t0002g0070 a0001c0001t0002g0099 others(4): Show |
7 | HG00735.hp1 HG01433.hp2 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.314-26409dupT | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148717193 | ||||||
| chr2:148717193 | AT | A | 152 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(149): Show |
153 | HG00280.hp1 HG00544.hp1 HG00544.hp2 others(150): Show |
intron_variant | MODIFIER | c.314-26409delT | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148717193 | ||||||
| chr2:148717193 | ATT | A | 31 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0010 others(28): Show |
31 | HG00639.hp1 HG01069.hp2 HG01884.hp1 others(28): Show |
intron_variant | MODIFIER | c.314-26410_314-2640 others(6): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148717193 | ||||||
| chr2:148717395 | G | A | 4 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(1): Show |
4 | HG02145.hp1 HG02451.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.314-26227G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148717395 | |||||||
| chr2:148717425 | A | T | 1 | a0001c0001t0002g0070 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.314-26197A>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148717425 | |||||||
| chr2:148717434 | C | T | 3 | a0001c0001t0001g0036 a0001c0001t0001g0042 a0001c0001t0001g0043 |
3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.314-26188C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148717434 | |||||||
| chr2:148717667 | G | C | 20 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0001g0184 others(17): Show |
20 | HG00673.hp2 HG02074.hp2 HG04204.hp1 others(17): Show |
intron_variant | MODIFIER | c.314-25955G>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148717667 | |||||||
| chr2:148717817 | A | G | 95 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(92): Show |
95 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.314-25805A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148717817 | |||||||
| chr2:148717827 | T | C | 1 | a0001c0001t0002g0059 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.314-25795T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148717827 | |||||||
| chr2:148717844 | G | T | 2 | a0001c0001t0001g0274 a0001c0001t0001g0280 |
2 | HG02647.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.314-25778G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148717844 | |||||||
| chr2:148717996 | T | C | 1 | a0001c0001t0001g0250 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.314-25626T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148717996 | |||||||
| chr2:148718003 | C | T | 1 | a0001c0001t0001g0151 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.314-25619C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148718003 | |||||||
| chr2:148718112 | CTTTAT | C | 4 | a0001c0005t0001g0186 a0002c0002t0001g0253 a0002c0002t0001g0307 others(1): Show |
4 | HG02647.hp2 HG02965.hp1 NA20300.hp1 others(1): Show |
intron_variant | MODIFIER | c.314-25506_314-2550 others(9): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148718112 | ||||||
| chr2:148718168 | G | A | 107 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(104): Show |
107 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(104): Show |
intron_variant | MODIFIER | c.314-25454G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148718168 | |||||||
| chr2:148718178 | G | T | 1 | a0001c0001t0001g0304 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.314-25444G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148718178 | |||||||
| chr2:148718319 | C | A | 5 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0191 others(2): Show |
5 | HG02258.hp1 HG02886.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.314-25303C>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148718319 | |||||||
| chr2:148718711 | T | G | 1 | a0001c0001t0002g0128 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.314-24911T>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148718711 | |||||||
| chr2:148718959 | A | G | 118 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(115): Show |
119 | HG00280.hp2 HG00423.hp2 HG00544.hp2 others(116): Show |
intron_variant | MODIFIER | c.314-24663A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148718959 | |||||||
| chr2:148719099 | A | G | 1 | a0001c0001t0001g0251 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.314-24523A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148719099 | |||||||
| chr2:148719211 | T | C | 1 | a0001c0001t0001g0267 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.314-24411T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148719211 | |||||||
| chr2:148719268 | G | T | 4 | a0001c0001t0002g0060 a0001c0001t0002g0125 a0001c0001t0002g0126 others(1): Show |
4 | HG02027.hp1 HG02602.hp1 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.314-24354G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148719268 | |||||||
| chr2:148719493 | C | G | 1 | a0001c0001t0001g0193 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.314-24129C>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148719493 | |||||||
| chr2:148719628 | G | A | 1 | a0001c0001t0001g0240 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.314-23994G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148719628 | |||||||
| chr2:148719724 | C | T | 12 | a0001c0001t0001g0171 a0001c0001t0001g0189 a0001c0001t0001g0190 others(9): Show |
12 | HG00639.hp1 HG02109.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.314-23898C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148719724 | |||||||
| chr2:148719725 | G | A | 1 | a0001c0001t0002g0122 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.314-23897G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148719725 | |||||||
| chr2:148719797 | T | A | 1 | a0001c0001t0007g0217 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.314-23825T>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148719797 | |||||||
| chr2:148719799 | A | G | 2 | a0001c0001t0001g0281 a0001c0001t0001g0282 |
2 | HG02257.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.314-23823A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148719799 | |||||||
| chr2:148719961 | G | A | 111 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0134 others(108): Show |
111 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(108): Show |
intron_variant | MODIFIER | c.314-23661G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148719961 | |||||||
| chr2:148720135 | G | A | 9 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(6): Show |
9 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.314-23487G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148720135 | |||||||
| chr2:148720282 | C | T | 9 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(6): Show |
9 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.314-23340C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148720282 | |||||||
| chr2:148720420 | T | C | 122 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(119): Show |
123 | HG00280.hp2 HG00423.hp2 HG00544.hp2 others(120): Show |
intron_variant | MODIFIER | c.314-23202T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148720420 | |||||||
| chr2:148720454 | A | C | 122 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(119): Show |
123 | HG00280.hp2 HG00423.hp2 HG00544.hp2 others(120): Show |
intron_variant | MODIFIER | c.314-23168A>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148720454 | |||||||
| chr2:148720454 | A | G | 6 | a0001c0001t0001g0274 a0001c0001t0001g0275 a0001c0001t0001g0276 others(3): Show |
6 | HG02572.hp1 HG02615.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.314-23168A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148720454 | |||||||
| chr2:148720462 | C | T | 3 | a0001c0001t0002g0059 a0001c0001t0002g0111 a0001c0001t0002g0133 |
3 | HG00741.hp1 HG01496.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.314-23160C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148720462 | |||||||
| chr2:148720590 | C | T | 1 | a0001c0001t0001g0225 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.314-23032C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148720590 | |||||||
| chr2:148720768 | C | T | 2 | a0001c0001t0001g0244 a0001c0001t0001g0245 |
2 | HG01891.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.314-22854C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148720768 | |||||||
| chr2:148720822 | A | G | 2 | a0001c0001t0001g0203 a0001c0001t0001g0266 |
2 | HG02027.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.314-22800A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148720822 | |||||||
| chr2:148720899 | C | G | 6 | a0001c0001t0002g0041 a0001c0001t0002g0071 a0001c0001t0002g0076 others(3): Show |
6 | HG02132.hp2 NA18946.hp2 NA18972.hp2 others(3): Show |
intron_variant | MODIFIER | c.314-22723C>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148720899 | |||||||
| chr2:148720967 | A | G | 1 | a0001c0001t0001g0277 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.314-22655A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148720967 | |||||||
| chr2:148721126 | C | T | 6 | a0001c0001t0001g0267 a0001c0001t0001g0271 a0001c0001t0001g0272 others(3): Show |
6 | HG01884.hp1 HG02109.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.314-22496C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148721126 | |||||||
| chr2:148721214 | G | T | 1 | a0001c0001t0002g0111 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.314-22408G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148721214 | |||||||
| chr2:148721250 | T | A | 3 | a0001c0001t0001g0036 a0001c0001t0001g0042 a0001c0001t0001g0043 |
3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.314-22372T>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148721250 | |||||||
| chr2:148721328 | GT | G | 10 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(7): Show |
10 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(7): Show |
intron_variant | MODIFIER | c.314-22283delT | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148721328 | ||||||
| chr2:148721501 | A | G | 1 | a0001c0001t0001g0304 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.314-22121A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148721501 | |||||||
| chr2:148721607 | A | G | 95 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(92): Show |
95 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.314-22015A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148721607 | |||||||
| chr2:148721712 | C | CT | 93 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0136 others(90): Show |
94 | HG00423.hp1 HG00544.hp1 HG00544.hp2 others(91): Show |
intron_variant | MODIFIER | c.314-21893dupT | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148721712 | ||||||
| chr2:148721712 | CT | C | 11 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(8): Show |
11 | HG00639.hp2 HG01175.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.314-21893delT | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148721712 | ||||||
| chr2:148721712 | CTT | C | 90 | a0001c0001t0002g0037 a0001c0001t0002g0038 a0001c0001t0002g0040 others(87): Show |
90 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.314-21894_314-2189 others(6): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148721712 | ||||||
| chr2:148721840 | A | G | 1 | a0001c0001t0001g0193 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.314-21782A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148721840 | |||||||
| chr2:148721890 | C | CT | 32 | a0001c0001t0001g0137 a0001c0001t0001g0158 a0001c0001t0001g0162 others(29): Show |
32 | HG00280.hp1 HG00639.hp1 HG01256.hp1 others(29): Show |
intron_variant | MODIFIER | c.314-21715dupT | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148721890 | ||||||
| chr2:148721890 | C | CTT | 85 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0134 others(82): Show |
85 | HG00423.hp1 HG00544.hp1 HG00609.hp1 others(82): Show |
intron_variant | MODIFIER | c.314-21716_314-2171 others(6): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148721890 | ||||||
| chr2:148721890 | C | CTTT | 101 | a0001c0001t0001g0136 a0001c0001t0001g0139 a0001c0001t0001g0141 others(98): Show |
102 | HG00280.hp2 HG00423.hp2 HG00544.hp2 others(99): Show |
intron_variant | MODIFIER | c.314-21717_314-2171 others(7): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148721890 | ||||||
| chr2:148721890 | C | CTTTT | 16 | a0001c0001t0001g0255 a0001c0001t0001g0292 a0001c0001t0001g0299 others(13): Show |
16 | HG00735.hp2 HG01106.hp1 HG01981.hp2 others(13): Show |
intron_variant | MODIFIER | c.314-21718_314-2171 others(8): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148721890 | ||||||
| chr2:148721890 | C | CTTTTT | 18 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0001g0184 others(15): Show |
18 | HG00673.hp2 HG02074.hp2 HG04204.hp1 others(15): Show |
intron_variant | MODIFIER | c.314-21719_314-2171 others(9): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148721890 | ||||||
| chr2:148721890 | C | CTTTTTTT others(1): Show |
9 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0033 others(6): Show |
9 | HG02040.hp2 HG02809.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.314-21722_314-2171 others(12): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148721890 | ||||||
| chr2:148721890 | C | CTTTTTTT others(3): Show |
1 | a0001c0001t0001g0252 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.314-21724_314-2171 others(14): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148721890 | ||||||
| chr2:148721891 | T | TTTC | 10 | a0001c0001t0001g0028 a0001c0001t0001g0274 a0001c0001t0001g0275 others(7): Show |
10 | HG02257.hp1 HG02572.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.314-21729_314-2172 others(7): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148721891 | ||||||
| chr2:148722024 | C | T | 1 | a0001c0001t0001g0240 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.314-21598C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148722024 | |||||||
| chr2:148722118 | C | T | 10 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(7): Show |
10 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(7): Show |
intron_variant | MODIFIER | c.314-21504C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148722118 | |||||||
| chr2:148722146 | G | A | 1 | a0001c0001t0001g0134 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.314-21476G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148722146 | |||||||
| chr2:148722166 | G | A | 2 | a0001c0001t0001g0198 a0001c0001t0001g0199 |
2 | HG02818.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.314-21456G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148722166 | |||||||
| chr2:148722267 | G | A | 1 | a0001c0001t0001g0155 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.314-21355G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148722267 | |||||||
| chr2:148722448 | G | T | 3 | a0001c0001t0001g0036 a0001c0001t0001g0042 a0001c0001t0001g0043 |
3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.314-21174G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148722448 | |||||||
| chr2:148722596 | C | T | 3 | a0001c0001t0001g0036 a0001c0001t0001g0042 a0001c0001t0001g0043 |
3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.314-21026C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148722596 | |||||||
| chr2:148722629 | A | G | 9 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(6): Show |
9 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.314-20993A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148722629 | |||||||
| chr2:148722747 | C | T | 3 | a0001c0001t0001g0036 a0001c0001t0001g0042 a0001c0001t0001g0043 |
3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.314-20875C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148722747 | |||||||
| chr2:148722852 | G | A | 1 | a0001c0001t0001g0304 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.314-20770G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148722852 | |||||||
| chr2:148722867 | G | A | 1 | a0001c0001t0002g0092 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.314-20755G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148722867 | |||||||
| chr2:148723022 | T | C | 1 | a0001c0005t0001g0009 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.314-20600T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148723022 | |||||||
| chr2:148723180 | T | C | 3 | a0001c0001t0002g0055 a0001c0001t0002g0056 a0001c0001t0002g0057 |
3 | HG01106.hp1 HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.314-20442T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148723180 | |||||||
| chr2:148723258 | A | G | 9 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(6): Show |
9 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.314-20364A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148723258 | |||||||
| chr2:148723369 | C | T | 9 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(6): Show |
9 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.314-20253C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148723369 | |||||||
| chr2:148723406 | C | G | 1 | a0001c0001t0002g0125 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.314-20216C>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148723406 | |||||||
| chr2:148723473 | C | G | 91 | a0001c0001t0002g0037 a0001c0001t0002g0038 a0001c0001t0002g0040 others(88): Show |
91 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.314-20149C>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148723473 | |||||||
| chr2:148723493 | G | A | 4 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0001g0184 others(1): Show |
4 | NA18954.hp2 NA19001.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.314-20129G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148723493 | |||||||
| chr2:148723552 | C | T | 1 | a0001c0001t0001g0246 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.314-20070C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148723552 | |||||||
| chr2:148723657 | T | A | 3 | a0001c0001t0001g0036 a0001c0001t0001g0042 a0001c0001t0001g0043 |
3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.314-19965T>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148723657 | |||||||
| chr2:148723756 | G | A | 2 | a0001c0001t0001g0281 a0001c0001t0001g0282 |
2 | HG02257.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.314-19866G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148723756 | |||||||
| chr2:148723814 | C | T | 4 | a0001c0005t0001g0186 a0002c0002t0001g0253 a0002c0002t0001g0307 others(1): Show |
4 | HG02647.hp2 HG02965.hp1 NA20300.hp1 others(1): Show |
intron_variant | MODIFIER | c.314-19808C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148723814 | |||||||
| chr2:148723885 | T | C | 3 | a0001c0001t0001g0250 a0001c0001t0001g0251 a0001c0001t0001g0252 |
3 | HG02572.hp2 HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.314-19737T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148723885 | |||||||
| chr2:148723906 | T | A | 290 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(287): Show |
291 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(288): Show |
intron_variant | MODIFIER | c.314-19716T>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148723906 | |||||||
| chr2:148724074 | G | T | 9 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(6): Show |
9 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.314-19548G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148724074 | |||||||
| chr2:148724101 | T | TTATAATC others(7): Show |
1 | a0001c0001t0001g0034 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.314-19508_314-1950 others(18): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148724101 | ||||||
| chr2:148724192 | G | C | 1 | a0001c0001t0001g0278 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.314-19430G>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148724192 | |||||||
| chr2:148724236 | A | T | 107 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(104): Show |
107 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(104): Show |
intron_variant | MODIFIER | c.314-19386A>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148724236 | |||||||
| chr2:148724342 | G | A | 2 | a0001c0001t0001g0255 a0001c0006t0001g0007 |
2 | HG00735.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.314-19280G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148724342 | |||||||
| chr2:148724386 | T | C | 3 | a0001c0001t0001g0036 a0001c0001t0001g0042 a0001c0001t0001g0043 |
3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.314-19236T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148724386 | |||||||
| chr2:148724387 | G | A | 1 | a0001c0001t0002g0050 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.314-19235G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148724387 | |||||||
| chr2:148724621 | G | A | 290 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(287): Show |
291 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(288): Show |
intron_variant | MODIFIER | c.314-19001G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148724621 | |||||||
| chr2:148724767 | A | G | 1 | a0001c0001t0001g0225 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.314-18855A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148724767 | |||||||
| chr2:148724822 | G | A | 3 | a0001c0001t0001g0036 a0001c0001t0001g0042 a0001c0001t0001g0043 |
3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.314-18800G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148724822 | |||||||
| chr2:148724889 | C | T | 91 | a0001c0001t0002g0037 a0001c0001t0002g0038 a0001c0001t0002g0040 others(88): Show |
91 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.314-18733C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148724889 | |||||||
| chr2:148724920 | A | G | 1 | a0001c0001t0001g0251 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.314-18702A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148724920 | |||||||
| chr2:148725040 | G | C | 2 | a0001c0001t0001g0281 a0001c0001t0001g0282 |
2 | HG02257.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.314-18582G>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148725040 | |||||||
| chr2:148725096 | C | G | 1 | a0001c0001t0001g0166 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.314-18526C>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148725096 | |||||||
| chr2:148725293 | G | A | 3 | a0001c0001t0001g0036 a0001c0001t0001g0042 a0001c0001t0001g0043 |
3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.314-18329G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148725293 | |||||||
| chr2:148725615 | C | A | 290 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(287): Show |
291 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(288): Show |
intron_variant | MODIFIER | c.314-18007C>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148725615 | |||||||
| chr2:148725764 | C | T | 10 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(7): Show |
10 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(7): Show |
intron_variant | MODIFIER | c.314-17858C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148725764 | |||||||
| chr2:148725884 | A | G | 2 | a0001c0001t0002g0064 a0001c0001t0002g0065 |
2 | NA18941.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.314-17738A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148725884 | |||||||
| chr2:148726098 | C | A | 20 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0001g0184 others(17): Show |
20 | HG00673.hp2 HG02074.hp2 HG04204.hp1 others(17): Show |
intron_variant | MODIFIER | c.314-17524C>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148726098 | |||||||
| chr2:148726136 | T | G | 1 | a0001c0001t0008g0039 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.314-17486T>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148726136 | |||||||
| chr2:148726187 | A | G | 1 | a0001c0001t0001g0036 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.314-17435A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148726187 | |||||||
| chr2:148726269 | G | A | 8 | a0001c0001t0001g0265 a0001c0001t0001g0267 a0001c0001t0001g0271 others(5): Show |
8 | HG01884.hp1 HG02109.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.314-17353G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148726269 | |||||||
| chr2:148726299 | T | C | 1 | a0001c0001t0002g0110 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.314-17323T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148726299 | |||||||
| chr2:148726358 | T | A | 1 | a0001c0001t0001g0304 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.314-17264T>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148726358 | |||||||
| chr2:148726396 | C | G | 111 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(108): Show |
111 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(108): Show |
intron_variant | MODIFIER | c.314-17226C>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148726396 | |||||||
| chr2:148726556 | T | G | 91 | a0001c0001t0002g0037 a0001c0001t0002g0038 a0001c0001t0002g0040 others(88): Show |
91 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.314-17066T>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148726556 | |||||||
| chr2:148726765 | G | GT | 101 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0010 others(98): Show |
102 | HG00280.hp1 HG00544.hp2 HG00609.hp2 others(99): Show |
intron_variant | MODIFIER | c.314-16843dupT | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148726765 | ||||||
| chr2:148726765 | G | T | 2 | a0001c0001t0001g0240 a0002c0002t0001g0307 |
2 | HG02109.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.314-16857G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148726765 | |||||||
| chr2:148726767 | T | G | 3 | a0001c0001t0001g0036 a0001c0001t0001g0042 a0001c0001t0001g0043 |
3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.314-16855T>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148726767 | |||||||
| chr2:148726841 | A | C | 1 | a0001c0001t0001g0170 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.314-16781A>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148726841 | |||||||
| chr2:148727165 | C | T | 9 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(6): Show |
9 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.314-16457C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148727165 | |||||||
| chr2:148727196 | C | A | 1 | a0001c0001t0001g0229 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.314-16426C>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148727196 | |||||||
| chr2:148727212 | G | C | 12 | a0001c0001t0001g0171 a0001c0001t0001g0189 a0001c0001t0001g0190 others(9): Show |
12 | HG00639.hp1 HG02109.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.314-16410G>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148727212 | |||||||
| chr2:148727370 | A | G | 164 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0134 others(161): Show |
165 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(162): Show |
intron_variant | MODIFIER | c.314-16252A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148727370 | |||||||
| chr2:148727471 | T | C | 1 | a0001c0005t0001g0186 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.314-16151T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148727471 | |||||||
| chr2:148727546 | G | A | 110 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(107): Show |
110 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(107): Show |
intron_variant | MODIFIER | c.314-16076G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148727546 | |||||||
| chr2:148727580 | G | A | 1 | a0001c0001t0002g0067 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.314-16042G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148727580 | |||||||
| chr2:148727706 | G | A | 110 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(107): Show |
110 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(107): Show |
intron_variant | MODIFIER | c.314-15916G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148727706 | |||||||
| chr2:148727792 | T | G | 1 | a0001c0001t0001g0304 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.314-15830T>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148727792 | |||||||
| chr2:148727879 | T | A | 1 | a0001c0001t0001g0205 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.314-15743T>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148727879 | |||||||
| chr2:148727880 | C | CA | 9 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(6): Show |
9 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.314-15741dupA | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148727880 | ||||||
| chr2:148728104 | C | T | 9 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(6): Show |
9 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.314-15518C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148728104 | |||||||
| chr2:148728244 | A | G | 91 | a0001c0001t0002g0037 a0001c0001t0002g0038 a0001c0001t0002g0040 others(88): Show |
91 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.314-15378A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148728244 | |||||||
| chr2:148728301 | TTTTG | T | 35 | a0001c0001t0001g0135 a0001c0001t0001g0174 a0001c0001t0001g0175 others(32): Show |
36 | HG00544.hp2 HG00609.hp2 HG00673.hp2 others(33): Show |
intron_variant | MODIFIER | c.314-15305_314-1530 others(8): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148728301 | ||||||
| chr2:148728365 | A | G | 15 | a0001c0001t0001g0289 a0001c0001t0001g0290 a0001c0001t0001g0291 others(12): Show |
15 | HG00673.hp2 HG02074.hp2 NA18949.hp2 others(12): Show |
intron_variant | MODIFIER | c.314-15257A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148728365 | |||||||
| chr2:148728517 | A | G | 1 | a0001c0001t0001g0267 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.314-15105A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148728517 | |||||||
| chr2:148728615 | A | G | 4 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(1): Show |
4 | HG00639.hp2 HG02809.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.314-15007A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148728615 | |||||||
| chr2:148728629 | C | T | 1 | a0001c0001t0001g0178 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.314-14993C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148728629 | |||||||
| chr2:148728675 | A | AGCCATGA others(2): Show |
95 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(92): Show |
95 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.314-14945_314-1493 others(13): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148728675 | ||||||
| chr2:148728729 | C | CT | 23 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(20): Show |
23 | HG00673.hp2 HG02074.hp2 HG02145.hp1 others(20): Show |
intron_variant | MODIFIER | c.314-14879dupT | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148728729 | ||||||
| chr2:148728743 | TA | T | 14 | a0001c0001t0001g0029 a0001c0001t0001g0135 a0001c0001t0001g0191 others(11): Show |
14 | HG00558.hp2 HG01496.hp2 HG01515.hp2 others(11): Show |
intron_variant | MODIFIER | c.314-14872delA | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148728743 | ||||||
| chr2:148728744 | A | T | 276 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(273): Show |
277 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(274): Show |
intron_variant | MODIFIER | c.314-14878A>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148728744 | |||||||
| chr2:148728745 | A | T | 1 | a0001c0001t0001g0247 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.314-14877A>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148728745 | |||||||
| chr2:148728754 | C | T | 6 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0191 others(3): Show |
6 | HG02109.hp2 HG02258.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.314-14868C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148728754 | |||||||
| chr2:148728815 | G | A | 11 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0178 others(8): Show |
12 | HG00544.hp2 HG00609.hp2 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.314-14807G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148728815 | |||||||
| chr2:148728894 | T | C | 4 | a0001c0005t0001g0186 a0002c0002t0001g0253 a0002c0002t0001g0307 others(1): Show |
4 | HG02647.hp2 HG02965.hp1 NA20300.hp1 others(1): Show |
intron_variant | MODIFIER | c.314-14728T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148728894 | |||||||
| chr2:148728954 | C | T | 1 | a0002c0002t0001g0253 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.314-14668C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148728954 | |||||||
| chr2:148728986 | C | G | 1 | a0001c0001t0001g0279 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.314-14636C>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148728986 | |||||||
| chr2:148728988 | C | T | 1 | a0001c0001t0001g0020 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.314-14634C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148728988 | |||||||
| chr2:148728992 | A | T | 1 | a0001c0001t0001g0240 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.314-14630A>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148728992 | |||||||
| chr2:148729011 | G | A | 1 | a0001c0001t0001g0302 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.314-14611G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148729011 | |||||||
| chr2:148729031 | C | CA | 78 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(75): Show |
78 | HG00642.hp1 HG00673.hp2 HG00738.hp1 others(75): Show |
intron_variant | MODIFIER | c.314-14565dupA | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148729031 | ||||||
| chr2:148729031 | C | CAA | 26 | a0001c0001t0001g0182 a0001c0001t0001g0187 a0001c0001t0001g0203 others(23): Show |
26 | HG00280.hp1 HG00609.hp1 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.314-14566_314-1456 others(6): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148729031 | ||||||
| chr2:148729031 | CA | C | 6 | a0001c0001t0001g0028 a0001c0001t0001g0135 a0001c0001t0001g0180 others(3): Show |
6 | HG01106.hp2 HG02818.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.314-14565delA | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148729031 | ||||||
| chr2:148729031 | CAA | C | 15 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0178 others(12): Show |
16 | HG00544.hp2 HG00609.hp2 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.314-14566_314-1456 others(6): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148729031 | ||||||
| chr2:148729031 | CAAAAAA | C | 12 | a0001c0001t0001g0171 a0001c0001t0001g0189 a0001c0001t0001g0190 others(9): Show |
12 | HG00639.hp1 HG02109.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.314-14570_314-1456 others(10): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148729031 | ||||||
| chr2:148729031 | CAAAAAAA others(1): Show |
C | 93 | a0001c0001t0001g0036 a0001c0001t0001g0042 a0001c0001t0001g0043 others(90): Show |
93 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.314-14572_314-1456 others(12): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148729031 | ||||||
| chr2:148729076 | C | A | 1 | a0001c0001t0001g0267 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.314-14546C>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148729076 | |||||||
| chr2:148729140 | C | T | 3 | a0001c0001t0005g0011 a0001c0001t0005g0210 a0001c0001t0005g0221 |
3 | HG01943.hp2 HG02273.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.314-14482C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148729140 | |||||||
| chr2:148729177 | A | G | 2 | a0001c0001t0001g0198 a0001c0001t0001g0199 |
2 | HG02818.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.314-14445A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148729177 | |||||||
| chr2:148729247 | A | G | 2 | a0001c0001t0001g0021 a0001c0001t0001g0022 |
2 | HG03195.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.314-14375A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148729247 | |||||||
| chr2:148729340 | C | T | 111 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0134 others(108): Show |
111 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(108): Show |
intron_variant | MODIFIER | c.314-14282C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148729340 | |||||||
| chr2:148729348 | T | G | 3 | a0001c0001t0001g0036 a0001c0001t0001g0042 a0001c0001t0001g0043 |
3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.314-14274T>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148729348 | |||||||
| chr2:148729481 | C | G | 1 | a0001c0001t0001g0288 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.314-14141C>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148729481 | |||||||
| chr2:148729621 | C | T | 95 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(92): Show |
95 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.314-14001C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148729621 | |||||||
| chr2:148729641 | A | G | 1 | a0001c0001t0001g0251 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.314-13981A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148729641 | |||||||
| chr2:148729775 | A | G | 95 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(92): Show |
95 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.314-13847A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148729775 | |||||||
| chr2:148730142 | A | G | 1 | a0001c0001t0001g0132 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.314-13480A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148730142 | |||||||
| chr2:148730268 | T | C | 1 | a0001c0001t0001g0170 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.314-13354T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148730268 | |||||||
| chr2:148730363 | G | A | 1 | a0001c0001t0001g0306 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.314-13259G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148730363 | |||||||
| chr2:148730420 | A | C | 91 | a0001c0001t0002g0037 a0001c0001t0002g0038 a0001c0001t0002g0040 others(88): Show |
91 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.314-13202A>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148730420 | |||||||
| chr2:148730650 | G | C | 2 | a0002c0002t0001g0307 a0002c0002t0006g0254 |
2 | HG02965.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.314-12972G>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148730650 | |||||||
| chr2:148730699 | C | A | 3 | a0001c0001t0001g0233 a0001c0001t0001g0234 a0001c0001t0001g0257 |
3 | HG01515.hp2 HG03831.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.314-12923C>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148730699 | |||||||
| chr2:148730741 | G | A | 1 | a0002c0002t0001g0253 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.314-12881G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148730741 | |||||||
| chr2:148730749 | T | G | 1 | a0002c0002t0001g0253 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.314-12873T>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148730749 | |||||||
| chr2:148730801 | A | G | 1 | a0001c0001t0001g0288 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.314-12821A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148730801 | |||||||
| chr2:148730809 | C | G | 1 | a0001c0001t0001g0272 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.314-12813C>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148730809 | |||||||
| chr2:148731036 | G | T | 1 | a0001c0001t0001g0134 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.314-12586G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148731036 | |||||||
| chr2:148731272 | C | T | 12 | a0001c0001t0001g0028 a0001c0001t0001g0274 a0001c0001t0001g0275 others(9): Show |
12 | HG02257.hp1 HG02257.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.314-12350C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148731272 | |||||||
| chr2:148731319 | C | T | 1 | a0001c0001t0001g0258 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.314-12303C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148731319 | |||||||
| chr2:148731521 | G | A | 1 | a0001c0001t0001g0134 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.314-12101G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148731521 | |||||||
| chr2:148731697 | C | T | 2 | a0001c0001t0002g0067 a0001c0001t0002g0069 |
2 | HG01884.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.314-11925C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148731697 | |||||||
| chr2:148731717 | C | T | 3 | a0001c0001t0001g0036 a0001c0001t0001g0042 a0001c0001t0001g0043 |
3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.314-11905C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148731717 | |||||||
| chr2:148731985 | T | C | 1 | a0001c0001t0001g0180 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.314-11637T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148731985 | |||||||
| chr2:148732027 | G | A | 1 | a0001c0001t0001g0229 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.314-11595G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148732027 | |||||||
| chr2:148732030 | A | G | 9 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(6): Show |
9 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.314-11592A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148732030 | |||||||
| chr2:148732131 | G | A | 1 | a0001c0001t0001g0184 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.314-11491G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148732131 | |||||||
| chr2:148732133 | A | G | 4 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0001g0184 others(1): Show |
4 | NA18954.hp2 NA19001.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.314-11489A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148732133 | |||||||
| chr2:148732253 | C | T | 11 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0178 others(8): Show |
12 | HG00544.hp2 HG00609.hp2 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.314-11369C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148732253 | |||||||
| chr2:148732381 | C | CT | 13 | a0001c0001t0001g0136 a0001c0001t0001g0156 a0001c0001t0001g0194 others(10): Show |
13 | HG00609.hp1 HG02071.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.314-11224dupT | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148732381 | ||||||
| chr2:148732381 | C | CTT | 90 | a0001c0001t0001g0250 a0001c0001t0002g0037 a0001c0001t0002g0038 others(87): Show |
90 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.314-11225_314-1122 others(6): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148732381 | ||||||
| chr2:148732386 | T | C | 8 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(5): Show |
8 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(5): Show |
intron_variant | MODIFIER | c.314-11236T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148732386 | |||||||
| chr2:148732531 | C | T | 3 | a0001c0001t0001g0250 a0001c0001t0001g0251 a0001c0001t0001g0252 |
3 | HG02572.hp2 HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.314-11091C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148732531 | |||||||
| chr2:148732542 | G | A | 9 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(6): Show |
9 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.314-11080G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148732542 | |||||||
| chr2:148732569 | T | C | 111 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0134 others(108): Show |
111 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(108): Show |
intron_variant | MODIFIER | c.314-11053T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148732569 | |||||||
| chr2:148732863 | A | G | 20 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0001g0184 others(17): Show |
20 | HG00673.hp2 HG02074.hp2 HG04204.hp1 others(17): Show |
intron_variant | MODIFIER | c.314-10759A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148732863 | |||||||
| chr2:148732919 | T | C | 1 | a0001c0001t0001g0196 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.314-10703T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148732919 | |||||||
| chr2:148732946 | C | CT | 118 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0012 others(115): Show |
119 | HG00280.hp1 HG00544.hp2 HG00558.hp1 others(116): Show |
intron_variant | MODIFIER | c.314-10656dupT | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148732946 | ||||||
| chr2:148732965 | TTC | T | 11 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0029 others(8): Show |
11 | HG02040.hp2 HG02132.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.314-10656_314-1065 others(6): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148732965 | |||||||
| chr2:148732966 | TC | T | 14 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(11): Show |
14 | HG00639.hp2 HG02109.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.314-10654delC | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148732966 | ||||||
| chr2:148732967 | C | T | 276 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0012 others(273): Show |
277 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(274): Show |
intron_variant | MODIFIER | c.314-10655C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148732967 | |||||||
| chr2:148733032 | CTTGAACT others(3): Show |
C | 1 | a0001c0001t0002g0101 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.314-10578_314-1056 others(14): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148733032 | ||||||
| chr2:148733074 | G | GAAGATTT others(320): Show |
1 | a0001c0001t0002g0079 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.314-10532_314-1053 others(331): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148733074 | ||||||
| chr2:148733074 | G | GAAGATTT others(320): Show |
1 | a0001c0001t0002g0072 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.314-10532_314-1053 others(331): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148733074 | ||||||
| chr2:148733074 | G | GAAGATTT others(320): Show |
1 | a0001c0001t0002g0080 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.314-10532_314-1053 others(331): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148733074 | ||||||
| chr2:148733074 | G | GAAGATTT others(319): Show |
2 | a0001c0001t0002g0107 a0001c0001t0003g0108 |
2 | NA18959.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.314-10532_314-1053 others(330): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148733074 | ||||||
| chr2:148733074 | G | GAAGATTT others(320): Show |
86 | a0001c0001t0002g0037 a0001c0001t0002g0038 a0001c0001t0002g0040 others(83): Show |
86 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(83): Show |
intron_variant | MODIFIER | c.314-10532_314-1053 others(331): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148733074 | ||||||
| chr2:148733148 | C | T | 1 | a0001c0001t0001g0036 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.314-10474C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148733148 | |||||||
| chr2:148733153 | G | C | 8 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(5): Show |
8 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(5): Show |
intron_variant | MODIFIER | c.314-10469G>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148733153 | |||||||
| chr2:148733164 | A | G | 2 | a0001c0001t0001g0281 a0001c0001t0001g0282 |
2 | HG02257.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.314-10458A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148733164 | |||||||
| chr2:148733186 | T | C | 24 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0196 others(21): Show |
24 | HG01256.hp2 HG01433.hp1 HG01943.hp2 others(21): Show |
intron_variant | MODIFIER | c.314-10436T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148733186 | |||||||
| chr2:148733240 | A | G | 1 | a0001c0001t0001g0175 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.314-10382A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148733240 | |||||||
| chr2:148733250 | T | C | 4 | a0001c0001t0002g0052 a0001c0001t0002g0061 a0001c0001t0002g0092 others(1): Show |
4 | HG03654.hp2 HG03942.hp1 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.314-10372T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148733250 | |||||||
| chr2:148733311 | C | T | 107 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(104): Show |
107 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(104): Show |
intron_variant | MODIFIER | c.314-10311C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148733311 | |||||||
| chr2:148733432 | T | C | 1 | a0001c0001t0002g0124 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.314-10190T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148733432 | |||||||
| chr2:148733473 | C | G | 11 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0178 others(8): Show |
12 | HG00544.hp2 HG00609.hp2 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.314-10149C>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148733473 | |||||||
| chr2:148733479 | A | AT | 26 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0019 others(23): Show |
26 | HG01123.hp1 HG01256.hp1 HG01258.hp2 others(23): Show |
intron_variant | MODIFIER | c.314-10107dupT | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148733479 | ||||||
| chr2:148733479 | A | ATT | 13 | a0001c0001t0001g0135 a0001c0001t0001g0139 a0001c0001t0001g0145 others(10): Show |
13 | HG00558.hp1 HG01891.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.314-10108_314-1010 others(6): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148733479 | ||||||
| chr2:148733479 | A | ATTT | 6 | a0001c0001t0001g0002 a0001c0001t0001g0136 a0001c0001t0001g0142 others(3): Show |
6 | HG02071.hp1 HG02080.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.314-10109_314-1010 others(7): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148733479 | ||||||
| chr2:148733479 | A | ATTTTTTT others(4): Show |
1 | a0001c0001t0001g0151 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.314-10117_314-1010 others(15): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148733479 | ||||||
| chr2:148733479 | A | ATTTTTTT others(5): Show |
3 | a0001c0001t0001g0021 a0001c0001t0001g0149 a0001c0001t0001g0150 |
3 | HG00423.hp1 HG03195.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.314-10118_314-1010 others(16): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148733479 | ||||||
| chr2:148733479 | A | ATTTTTTT others(6): Show |
1 | a0001c0001t0001g0023 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.314-10119_314-1010 others(17): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148733479 | ||||||
| chr2:148733479 | A | ATTTTTTT others(10): Show |
1 | a0001c0001t0001g0022 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.314-10123_314-1010 others(21): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148733479 | ||||||
| chr2:148733479 | A | ATTTTTTT others(11): Show |
1 | a0001c0001t0001g0012 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.314-10124_314-1010 others(22): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148733479 | ||||||
| chr2:148733479 | A | ATTTTTTT others(13): Show |
2 | a0001c0001t0001g0024 a0001c0001t0001g0211 |
2 | HG02922.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.314-10126_314-1010 others(24): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148733479 | ||||||
| chr2:148733479 | AT | A | 16 | a0001c0001t0001g0028 a0001c0001t0001g0171 a0001c0001t0001g0174 others(13): Show |
16 | HG00544.hp2 HG00639.hp1 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.314-10107delT | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148733479 | ||||||
| chr2:148733479 | ATT | A | 26 | a0001c0001t0001g0134 a0001c0001t0001g0170 a0001c0001t0001g0172 others(23): Show |
26 | HG00280.hp2 HG00609.hp2 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.314-10108_314-1010 others(6): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148733479 | ||||||
| chr2:148733479 | ATTT | A | 36 | a0001c0001t0001g0201 a0001c0001t0001g0204 a0001c0001t0001g0207 others(33): Show |
36 | HG00280.hp1 HG00609.hp1 HG01070.hp1 others(33): Show |
intron_variant | MODIFIER | c.314-10109_314-1010 others(7): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148733479 | ||||||
| chr2:148733479 | ATTTT | A | 10 | a0001c0001t0001g0015 a0001c0001t0001g0200 a0001c0001t0001g0206 others(7): Show |
10 | HG00741.hp2 HG01069.hp2 HG01106.hp1 others(7): Show |
intron_variant | MODIFIER | c.314-10110_314-1010 others(8): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148733479 | ||||||
| chr2:148733479 | ATTTTTT | A | 15 | a0001c0001t0001g0233 a0001c0001t0002g0061 a0001c0001t0002g0067 others(12): Show |
15 | HG02004.hp2 HG02027.hp1 HG02080.hp2 others(12): Show |
intron_variant | MODIFIER | c.314-10112_314-1010 others(10): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148733479 | ||||||
| chr2:148733479 | ATTTTTTT | A | 54 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(51): Show |
54 | HG00558.hp2 HG00639.hp2 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.314-10113_314-1010 others(11): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148733479 | ||||||
| chr2:148733479 | ATTTTTTT others(3): Show |
A | 18 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0032 others(15): Show |
18 | HG01884.hp1 HG02040.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.314-10116_314-1010 others(14): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148733479 | ||||||
| chr2:148733479 | ATTTTTTT others(4): Show |
A | 14 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0036 others(11): Show |
14 | HG00738.hp2 HG01069.hp1 HG01070.hp2 others(11): Show |
intron_variant | MODIFIER | c.314-10117_314-1010 others(15): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148733479 | ||||||
| chr2:148733479 | ATTTTTTT others(5): Show |
A | 2 | a0001c0001t0001g0289 a0001c0001t0001g0297 |
2 | NA18949.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.314-10118_314-1010 others(16): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148733479 | ||||||
| chr2:148733479 | ATTTTTTT others(6): Show |
A | 15 | a0001c0001t0001g0014 a0001c0001t0001g0185 a0001c0001t0001g0256 others(12): Show |
15 | HG00673.hp2 HG02074.hp2 HG02717.hp2 others(12): Show |
intron_variant | MODIFIER | c.314-10119_314-1010 others(17): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148733479 | ||||||
| chr2:148733479 | ATTTTTTT others(7): Show |
A | 5 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0001g0184 others(2): Show |
5 | HG02922.hp1 NA18954.hp2 NA18959.hp2 others(2): Show |
intron_variant | MODIFIER | c.314-10120_314-1010 others(18): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148733479 | ||||||
| chr2:148733479 | ATTTTTTT others(8): Show |
A | 1 | a0001c0001t0001g0273 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.314-10121_314-1010 others(19): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148733479 | ||||||
| chr2:148733479 | ATTTTTTT others(12): Show |
A | 3 | a0001c0001t0001g0137 a0001c0001t0001g0158 a0001c0001t0001g0159 |
3 | NA18969.hp1 NA19001.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.314-10125_314-1010 others(23): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148733479 | ||||||
| chr2:148733479 | ATTTTTTT others(13): Show |
A | 1 | a0001c0001t0002g0098 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.314-10126_314-1010 others(24): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148733479 | ||||||
| chr2:148733479 | ATTTTTTT others(14): Show |
A | 4 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(1): Show |
4 | HG02145.hp1 HG02451.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.314-10127_314-1010 others(25): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148733479 | ||||||
| chr2:148733515 | T | G | 1 | a0001c0001t0002g0120 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.314-10107T>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148733515 | |||||||
| chr2:148733613 | T | G | 1 | a0001c0001t0001g0003 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.314-10009T>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148733613 | |||||||
| chr2:148733680 | G | A | 3 | a0001c0001t0001g0036 a0001c0001t0001g0042 a0001c0001t0001g0043 |
3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.314-9942G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148733680 | |||||||
| chr2:148733754 | T | G | 1 | a0001c0001t0001g0240 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.314-9868T>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148733754 | |||||||
| chr2:148733866 | G | A | 12 | a0001c0001t0001g0171 a0001c0001t0001g0189 a0001c0001t0001g0190 others(9): Show |
12 | HG00639.hp1 HG02109.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.314-9756G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148733866 | |||||||
| chr2:148733893 | G | C | 1 | a0001c0001t0001g0304 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.314-9729G>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148733893 | |||||||
| chr2:148734013 | C | T | 2 | a0001c0001t0001g0231 a0001c0001t0001g0235 |
2 | HG02622.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.314-9609C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148734013 | |||||||
| chr2:148734014 | A | G | 1 | a0001c0001t0001g0306 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.314-9608A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148734014 | |||||||
| chr2:148734043 | A | G | 5 | a0001c0001t0003g0062 a0001c0001t0003g0084 a0001c0001t0003g0094 others(2): Show |
5 | HG00558.hp2 HG01981.hp2 HG02004.hp2 others(2): Show |
intron_variant | MODIFIER | c.314-9579A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148734043 | |||||||
| chr2:148734561 | G | T | 3 | a0001c0001t0001g0250 a0001c0001t0001g0251 a0001c0001t0001g0252 |
3 | HG02572.hp2 HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.314-9061G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148734561 | |||||||
| chr2:148734648 | T | C | 1 | a0001c0001t0002g0110 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.314-8974T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148734648 | |||||||
| chr2:148734803 | C | CT | 96 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(93): Show |
96 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(93): Show |
intron_variant | MODIFIER | c.314-8805dupT | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148734803 | ||||||
| chr2:148734803 | CT | C | 14 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0027 others(11): Show |
14 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(11): Show |
intron_variant | MODIFIER | c.314-8805delT | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148734803 | ||||||
| chr2:148735125 | T | C | 1 | a0001c0001t0001g0265 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.314-8497T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148735125 | |||||||
| chr2:148735170 | A | G | 35 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0178 others(32): Show |
36 | HG00544.hp2 HG00609.hp2 HG00673.hp2 others(33): Show |
intron_variant | MODIFIER | c.314-8452A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148735170 | |||||||
| chr2:148735307 | C | G | 2 | a0001c0001t0001g0017 a0001c0001t0001g0019 |
2 | HG02886.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.314-8315C>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148735307 | |||||||
| chr2:148735391 | C | T | 1 | a0001c0001t0002g0070 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.314-8231C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148735391 | |||||||
| chr2:148735471 | C | G | 7 | a0001c0001t0002g0063 a0001c0001t0002g0079 a0001c0001t0002g0088 others(4): Show |
7 | HG00673.hp1 HG02040.hp1 HG02080.hp2 others(4): Show |
intron_variant | MODIFIER | c.314-8151C>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148735471 | |||||||
| chr2:148735653 | A | C | 108 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(105): Show |
108 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(105): Show |
intron_variant | MODIFIER | c.314-7969A>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148735653 | |||||||
| chr2:148735728 | A | G | 1 | a0001c0001t0002g0080 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.314-7894A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148735728 | |||||||
| chr2:148735799 | T | C | 1 | a0001c0001t0002g0068 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.314-7823T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148735799 | |||||||
| chr2:148735830 | T | TATAAG | 111 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(108): Show |
111 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(108): Show |
intron_variant | MODIFIER | c.314-7791_314-7787d others(7): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148735830 | ||||||
| chr2:148736059 | G | A | 1 | a0001c0001t0001g0155 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.314-7563G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148736059 | |||||||
| chr2:148736578 | T | C | 2 | a0001c0004t0001g0013 a0001c0004t0001g0026 |
2 | HG01891.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.314-7044T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148736578 | |||||||
| chr2:148736655 | G | A | 108 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(105): Show |
108 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(105): Show |
intron_variant | MODIFIER | c.314-6967G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148736655 | |||||||
| chr2:148736836 | A | G | 95 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(92): Show |
95 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.314-6786A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148736836 | |||||||
| chr2:148736890 | A | G | 5 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0001c0003t0001g0249 others(2): Show |
5 | HG01884.hp1 HG02109.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.314-6732A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148736890 | |||||||
| chr2:148736894 | G | A | 2 | a0001c0001t0001g0281 a0001c0001t0001g0282 |
2 | HG02257.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.314-6728G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148736894 | |||||||
| chr2:148736921 | G | A | 1 | a0001c0001t0001g0192 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.314-6701G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148736921 | |||||||
| chr2:148736936 | C | CA | 6 | a0001c0001t0001g0143 a0001c0001t0001g0195 a0001c0001t0001g0286 others(3): Show |
6 | HG02922.hp1 HG03098.hp1 HG03942.hp1 others(3): Show |
intron_variant | MODIFIER | c.314-6670dupA | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148736936 | ||||||
| chr2:148736936 | CA | C | 11 | a0001c0001t0001g0238 a0001c0001t0002g0038 a0001c0001t0002g0053 others(8): Show |
11 | HG00280.hp2 HG00609.hp1 HG00741.hp1 others(8): Show |
intron_variant | MODIFIER | c.314-6670delA | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148736936 | ||||||
| chr2:148736997 | G | A | 3 | a0001c0001t0001g0250 a0001c0001t0001g0251 a0001c0001t0001g0252 |
3 | HG02572.hp2 HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.314-6625G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148736997 | |||||||
| chr2:148737078 | G | A | 1 | a0001c0001t0001g0267 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.314-6544G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148737078 | |||||||
| chr2:148737108 | T | G | 1 | a0001c0001t0001g0188 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.314-6514T>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148737108 | |||||||
| chr2:148737123 | GT | G | 4 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(1): Show |
4 | HG00639.hp2 HG02809.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.314-6492delT | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148737123 | ||||||
| chr2:148737174 | C | G | 4 | a0001c0001t0001g0171 a0001c0001t0001g0241 a0001c0001t0001g0242 others(1): Show |
4 | HG00639.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.314-6448C>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148737174 | |||||||
| chr2:148737209 | A | T | 3 | a0001c0001t0001g0036 a0001c0001t0001g0042 a0001c0001t0001g0043 |
3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.314-6413A>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148737209 | |||||||
| chr2:148737291 | C | T | 1 | a0001c0005t0001g0186 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.314-6331C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148737291 | |||||||
| chr2:148737368 | G | T | 4 | a0001c0001t0002g0079 a0001c0001t0002g0088 a0001c0001t0002g0089 others(1): Show |
4 | HG02080.hp2 NA18975.hp1 NA19077.hp2 others(1): Show |
intron_variant | MODIFIER | c.314-6254G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148737368 | |||||||
| chr2:148737369 | A | ATATTCTA others(21): Show |
4 | a0001c0001t0002g0079 a0001c0001t0002g0088 a0001c0001t0002g0089 others(1): Show |
4 | HG02080.hp2 NA18975.hp1 NA19077.hp2 others(1): Show |
intron_variant | MODIFIER | c.314-6253_314-6252i others(30): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148737369 | |||||||
| chr2:148737370 | G | A | 4 | a0001c0001t0002g0079 a0001c0001t0002g0088 a0001c0001t0002g0089 others(1): Show |
4 | HG02080.hp2 NA18975.hp1 NA19077.hp2 others(1): Show |
intron_variant | MODIFIER | c.314-6252G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148737370 | |||||||
| chr2:148737371 | G | T | 4 | a0001c0001t0002g0079 a0001c0001t0002g0088 a0001c0001t0002g0089 others(1): Show |
4 | HG02080.hp2 NA18975.hp1 NA19077.hp2 others(1): Show |
intron_variant | MODIFIER | c.314-6251G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148737371 | |||||||
| chr2:148737431 | T | C | 10 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(7): Show |
10 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(7): Show |
intron_variant | MODIFIER | c.314-6191T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148737431 | |||||||
| chr2:148737567 | G | A | 1 | a0001c0001t0001g0153 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.314-6055G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148737567 | |||||||
| chr2:148737687 | TA | T | 5 | a0001c0001t0004g0001 a0001c0001t0004g0173 a0001c0001t0004g0176 others(2): Show |
6 | HG00544.hp2 HG00609.hp2 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.314-5933delA | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148737687 | ||||||
| chr2:148737705 | C | T | 1 | a0001c0001t0001g0170 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.314-5917C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148737705 | |||||||
| chr2:148737950 | A | G | 12 | a0001c0001t0001g0028 a0001c0001t0001g0274 a0001c0001t0001g0275 others(9): Show |
12 | HG02257.hp1 HG02257.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.314-5672A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148737950 | |||||||
| chr2:148738041 | A | G | 1 | a0001c0001t0001g0262 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.314-5581A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148738041 | |||||||
| chr2:148738084 | C | T | 2 | a0001c0001t0001g0158 a0001c0001t0001g0159 |
2 | NA18969.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.314-5538C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148738084 | |||||||
| chr2:148738123 | A | AAAC | 98 | a0001c0001t0001g0003 a0001c0001t0001g0036 a0001c0001t0001g0042 others(95): Show |
98 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(95): Show |
intron_variant | MODIFIER | c.314-5478_314-5476d others(5): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148738123 | ||||||
| chr2:148738149 | A | T | 1 | a0001c0001t0008g0039 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.314-5473A>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148738149 | |||||||
| chr2:148738284 | T | C | 1 | a0001c0001t0002g0105 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.314-5338T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148738284 | |||||||
| chr2:148738528 | T | C | 3 | a0001c0001t0001g0036 a0001c0001t0001g0042 a0001c0001t0001g0043 |
3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.314-5094T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148738528 | |||||||
| chr2:148738609 | T | C | 1 | a0002c0002t0001g0253 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.314-5013T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148738609 | |||||||
| chr2:148738913 | C | T | 2 | a0001c0001t0001g0131 a0001c0001t0001g0132 |
2 | HG02809.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.314-4709C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148738913 | |||||||
| chr2:148738920 | G | A | 3 | a0001c0001t0001g0036 a0001c0001t0001g0042 a0001c0001t0001g0043 |
3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.314-4702G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148738920 | |||||||
| chr2:148738941 | C | G | 4 | a0001c0001t0002g0099 a0001c0001t0002g0100 a0001c0001t0002g0101 others(1): Show |
4 | NA18947.hp1 NA18952.hp2 NA19064.hp2 others(1): Show |
intron_variant | MODIFIER | c.314-4681C>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148738941 | |||||||
| chr2:148739138 | G | C | 10 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(7): Show |
10 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(7): Show |
intron_variant | MODIFIER | c.314-4484G>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148739138 | |||||||
| chr2:148739358 | C | T | 277 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(274): Show |
278 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(275): Show |
intron_variant | MODIFIER | c.314-4264C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148739358 | |||||||
| chr2:148739589 | T | C | 1 | a0001c0005t0001g0009 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.314-4033T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148739589 | |||||||
| chr2:148739750 | G | C | 289 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(286): Show |
290 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(287): Show |
intron_variant | MODIFIER | c.314-3872G>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148739750 | |||||||
| chr2:148739813 | C | T | 95 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(92): Show |
95 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.314-3809C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148739813 | |||||||
| chr2:148739830 | C | CT | 7 | a0001c0001t0001g0250 a0001c0001t0002g0037 a0001c0001t0002g0046 others(4): Show |
7 | HG01069.hp1 HG01070.hp2 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.314-3790dupT | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148739830 | ||||||
| chr2:148739830 | C | CTT | 54 | a0001c0001t0002g0041 a0001c0001t0002g0045 a0001c0001t0002g0047 others(51): Show |
54 | HG00280.hp2 HG00558.hp2 HG00735.hp1 others(51): Show |
intron_variant | MODIFIER | c.314-3791_314-3790d others(4): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148739830 | ||||||
| chr2:148739830 | C | CTTT | 22 | a0001c0001t0002g0038 a0001c0001t0002g0040 a0001c0001t0002g0044 others(19): Show |
22 | HG00642.hp2 HG00673.hp1 HG01433.hp2 others(19): Show |
intron_variant | MODIFIER | c.314-3790_314-3789i others(5): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148739830 | ||||||
| chr2:148739830 | C | CTTTT | 6 | a0001c0001t0002g0082 a0001c0001t0002g0098 a0001c0001t0002g0099 others(3): Show |
6 | HG00423.hp2 NA18985.hp1 NA19007.hp2 others(3): Show |
intron_variant | MODIFIER | c.314-3790_314-3789i others(6): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148739830 | ||||||
| chr2:148739830 | CTTCTTTT others(2): Show |
C | 7 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(4): Show |
7 | HG02132.hp1 HG02155.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.314-3789_314-3781d others(11): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148739830 | ||||||
| chr2:148739830 | CTTCTTTT others(3): Show |
C | 2 | a0001c0001t0001g0033 a0001c0001t0002g0095 |
2 | HG02040.hp1 HG02040.hp2 |
intron_variant | MODIFIER | c.314-3789_314-3780d others(12): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148739830 | ||||||
| chr2:148739833 | C | T | 90 | a0001c0001t0001g0250 a0001c0001t0002g0037 a0001c0001t0002g0038 others(87): Show |
90 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.314-3789C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148739833 | |||||||
| chr2:148739833 | CT | C | 14 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0015 others(11): Show |
14 | HG00673.hp2 HG01891.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.314-3764delT | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148739833 | ||||||
| chr2:148739833 | CTT | C | 41 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0134 others(38): Show |
42 | HG00280.hp1 HG00544.hp2 HG00609.hp2 others(39): Show |
intron_variant | MODIFIER | c.314-3765_314-3764d others(4): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148739833 | ||||||
| chr2:148739833 | CTTT | C | 119 | a0001c0001t0001g0005 a0001c0001t0001g0028 a0001c0001t0001g0136 others(116): Show |
119 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(116): Show |
intron_variant | MODIFIER | c.314-3766_314-3764d others(5): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148739833 | ||||||
| chr2:148739833 | CTTTT | C | 11 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(8): Show |
11 | HG01070.hp1 HG01515.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.314-3767_314-3764d others(6): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148739833 | ||||||
| chr2:148739833 | CTTTTTTT others(2): Show |
C | 6 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0001c0001t0001g0306 others(3): Show |
6 | HG01884.hp1 HG02109.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.314-3772_314-3764d others(11): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148739833 | ||||||
| chr2:148739836 | T | C | 1 | a0001c0001t0001g0267 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.314-3786T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148739836 | |||||||
| chr2:148739916 | G | A | 1 | a0001c0001t0001g0266 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.314-3706G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148739916 | |||||||
| chr2:148740093 | G | T | 2 | a0001c0001t0001g0198 a0001c0001t0001g0199 |
2 | HG02818.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.314-3529G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148740093 | |||||||
| chr2:148740241 | T | C | 2 | a0001c0001t0001g0198 a0001c0001t0001g0199 |
2 | HG02818.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.314-3381T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148740241 | |||||||
| chr2:148740342 | G | A | 2 | a0001c0001t0001g0231 a0001c0001t0001g0235 |
2 | HG02622.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.314-3280G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148740342 | |||||||
| chr2:148740531 | T | C | 1 | a0001c0001t0001g0226 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.314-3091T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148740531 | |||||||
| chr2:148741053 | T | G | 1 | a0001c0001t0001g0225 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.314-2569T>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148741053 | |||||||
| chr2:148741433 | C | A | 110 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(107): Show |
110 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(107): Show |
intron_variant | MODIFIER | c.314-2189C>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148741433 | |||||||
| chr2:148741499 | G | A | 1 | a0001c0001t0008g0039 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.314-2123G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148741499 | |||||||
| chr2:148741552 | A | G | 1 | a0001c0001t0002g0070 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.314-2070A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148741552 | |||||||
| chr2:148741653 | A | G | 1 | a0001c0001t0008g0039 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.314-1969A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148741653 | |||||||
| chr2:148741745 | T | A | 4 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(1): Show |
4 | HG00639.hp2 HG02809.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.314-1877T>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148741745 | |||||||
| chr2:148741930 | C | T | 2 | a0002c0002t0001g0307 a0002c0002t0006g0254 |
2 | HG02965.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.314-1692C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148741930 | |||||||
| chr2:148741991 | A | G | 95 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(92): Show |
95 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.314-1631A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148741991 | |||||||
| chr2:148742149 | A | G | 1 | a0001c0001t0001g0152 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.314-1473A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148742149 | |||||||
| chr2:148742348 | G | A | 2 | a0001c0001t0001g0198 a0001c0001t0001g0199 |
2 | HG02818.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.314-1274G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148742348 | |||||||
| chr2:148742474 | GGT | G | 107 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(104): Show |
107 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(104): Show |
intron_variant | MODIFIER | c.314-1142_314-1141d others(4): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148742474 | ||||||
| chr2:148742532 | C | G | 13 | a0001c0001t0001g0137 a0001c0001t0001g0140 a0001c0001t0001g0155 others(10): Show |
13 | HG02135.hp1 NA18747.hp1 NA18941.hp1 others(10): Show |
intron_variant | MODIFIER | c.314-1090C>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148742532 | |||||||
| chr2:148742567 | G | A | 1 | a0001c0001t0001g0227 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.314-1055G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148742567 | |||||||
| chr2:148742707 | A | G | 2 | a0001c0004t0001g0013 a0001c0004t0001g0026 |
2 | HG01891.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.314-915A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148742707 | |||||||
| chr2:148742736 | G | A | 6 | a0001c0001t0001g0274 a0001c0001t0001g0275 a0001c0001t0001g0276 others(3): Show |
6 | HG02572.hp1 HG02615.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.314-886G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148742736 | |||||||
| chr2:148742784 | C | CA | 135 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(132): Show |
136 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(133): Show |
intron_variant | MODIFIER | c.314-822dupA | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148742784 | ||||||
| chr2:148742784 | CA | C | 93 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(90): Show |
93 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.314-822delA | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 148742784 | ||||||
| chr2:148742844 | A | T | 9 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(6): Show |
9 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.314-778A>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148742844 | |||||||
| chr2:148743213 | A | G | 3 | a0001c0001t0001g0036 a0001c0001t0001g0042 a0001c0001t0001g0043 |
3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.314-409A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148743213 | |||||||
| chr2:148743246 | A | G | 3 | a0001c0001t0001g0036 a0001c0001t0001g0042 a0001c0001t0001g0043 |
3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.314-376A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148743246 | |||||||
| chr2:148743375 | A | T | 1 | a0001c0001t0001g0195 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.314-247A>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148743375 | |||||||
| chr2:148743434 | T | C | 1 | a0001c0001t0001g0135 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.314-188T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148743434 | |||||||
| chr2:148743566 | C | A | 9 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(6): Show |
9 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.314-56C>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 2/13 | chr2 | 148743566 | |||||||
| chr2:148743861 | A | C | 2 | a0001c0001t0001g0251 a0001c0001t0001g0252 |
2 | HG02572.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.459+94A>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148743861 | |||||||
| chr2:148743981 | A | T | 1 | a0001c0001t0002g0058 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.459+214A>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148743981 | |||||||
| chr2:148744279 | C | G | 11 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0178 others(8): Show |
12 | HG00544.hp2 HG00609.hp2 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.459+512C>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148744279 | |||||||
| chr2:148744572 | A | G | 20 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0001g0184 others(17): Show |
20 | HG00673.hp2 HG02074.hp2 HG04204.hp1 others(17): Show |
intron_variant | MODIFIER | c.459+805A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148744572 | |||||||
| chr2:148744587 | G | A | 3 | a0001c0001t0001g0036 a0001c0001t0001g0042 a0001c0001t0001g0043 |
3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.459+820G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148744587 | |||||||
| chr2:148744789 | AATTGTTA others(5): Show |
A | 2 | a0001c0001t0001g0236 a0001c0001t0001g0237 |
2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.459+1026_459+1037d others(14): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 148744789 | ||||||
| chr2:148744813 | T | TTAGAGA | 111 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(108): Show |
111 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(108): Show |
intron_variant | MODIFIER | c.459+1051_459+1052i others(8): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 148744813 | ||||||
| chr2:148744844 | T | C | 1 | a0001c0001t0001g0304 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.459+1077T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148744844 | |||||||
| chr2:148744873 | A | G | 1 | a0001c0001t0002g0097 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.459+1106A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148744873 | |||||||
| chr2:148744977 | G | A | 1 | a0001c0001t0002g0133 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.459+1210G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148744977 | |||||||
| chr2:148744989 | G | GC | 63 | a0001c0001t0001g0021 a0001c0001t0001g0032 a0001c0001t0001g0129 others(60): Show |
63 | HG00423.hp1 HG00558.hp1 HG01106.hp2 others(60): Show |
intron_variant | MODIFIER | c.459+1234dupC | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 148744989 | ||||||
| chr2:148744989 | G | GCC | 40 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0136 others(37): Show |
41 | HG00544.hp1 HG00558.hp2 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.459+1233_459+1234d others(4): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 148744989 | ||||||
| chr2:148744989 | G | GCCC | 32 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0155 others(29): Show |
32 | HG00544.hp2 HG00609.hp1 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.459+1232_459+1234d others(5): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 148744989 | ||||||
| chr2:148744989 | G | GCCCC | 33 | a0001c0001t0001g0005 a0001c0001t0001g0188 a0001c0001t0001g0196 others(30): Show |
33 | HG00280.hp1 HG00609.hp2 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.459+1231_459+1234d others(6): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 148744989 | ||||||
| chr2:148744989 | GC | G | 17 | a0001c0001t0001g0010 a0001c0001t0001g0025 a0001c0001t0001g0030 others(14): Show |
17 | HG00639.hp1 HG01123.hp1 HG02040.hp2 others(14): Show |
intron_variant | MODIFIER | c.459+1234delC | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 148744989 | ||||||
| chr2:148744994 | C | T | 1 | a0001c0001t0002g0097 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.459+1227C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148744994 | |||||||
| chr2:148744997 | C | T | 1 | a0001c0001t0001g0198 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.459+1230C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148744997 | |||||||
| chr2:148745147 | G | C | 5 | a0001c0001t0004g0001 a0001c0001t0004g0173 a0001c0001t0004g0176 others(2): Show |
6 | HG00544.hp2 HG00609.hp2 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.459+1380G>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148745147 | |||||||
| chr2:148745150 | G | A | 3 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0191 |
3 | HG02258.hp1 HG03098.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.459+1383G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148745150 | |||||||
| chr2:148745191 | A | G | 105 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(102): Show |
105 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(102): Show |
intron_variant | MODIFIER | c.459+1424A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148745191 | |||||||
| chr2:148745193 | C | T | 1 | a0001c0001t0001g0028 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.459+1426C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148745193 | |||||||
| chr2:148745202 | C | T | 1 | a0001c0001t0001g0028 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.459+1435C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148745202 | |||||||
| chr2:148745288 | A | G | 3 | a0001c0001t0001g0250 a0001c0001t0001g0251 a0001c0001t0001g0252 |
3 | HG02572.hp2 HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.459+1521A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148745288 | |||||||
| chr2:148745421 | G | A | 1 | a0001c0001t0001g0032 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.459+1654G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148745421 | |||||||
| chr2:148745431 | C | T | 163 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0134 others(160): Show |
164 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(161): Show |
intron_variant | MODIFIER | c.459+1664C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148745431 | |||||||
| chr2:148745789 | G | A | 8 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(5): Show |
8 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(5): Show |
intron_variant | MODIFIER | c.459+2022G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148745789 | |||||||
| chr2:148745848 | C | T | 2 | a0001c0001t0002g0125 a0001c0001t0002g0126 |
2 | HG02027.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.459+2081C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148745848 | |||||||
| chr2:148745862 | C | G | 3 | a0001c0001t0001g0036 a0001c0001t0001g0042 a0001c0001t0001g0043 |
3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.459+2095C>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148745862 | |||||||
| chr2:148745925 | C | G | 1 | a0001c0001t0001g0002 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.459+2158C>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148745925 | |||||||
| chr2:148745928 | T | C | 10 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(7): Show |
10 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(7): Show |
intron_variant | MODIFIER | c.459+2161T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148745928 | |||||||
| chr2:148745943 | A | G | 3 | a0001c0001t0001g0232 a0001c0001t0001g0263 a0001c0001t0001g0264 |
3 | NA18612.hp2 NA18975.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.459+2176A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148745943 | |||||||
| chr2:148746033 | A | G | 1 | a0001c0001t0002g0122 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.459+2266A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148746033 | |||||||
| chr2:148746193 | G | A | 6 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0191 others(3): Show |
6 | HG02109.hp2 HG02258.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.459+2426G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148746193 | |||||||
| chr2:148746226 | C | A | 3 | a0001c0001t0001g0036 a0001c0001t0001g0042 a0001c0001t0001g0043 |
3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.459+2459C>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148746226 | |||||||
| chr2:148746431 | T | C | 2 | a0001c0001t0001g0187 a0001c0001t0001g0248 |
2 | HG02717.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.459+2664T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148746431 | |||||||
| chr2:148746441 | G | A | 2 | a0001c0001t0001g0131 a0001c0001t0001g0132 |
2 | HG02809.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.459+2674G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148746441 | |||||||
| chr2:148746541 | G | A | 107 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(104): Show |
107 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(104): Show |
intron_variant | MODIFIER | c.459+2774G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148746541 | |||||||
| chr2:148746780 | G | A | 9 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(6): Show |
9 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.459+3013G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148746780 | |||||||
| chr2:148746822 | T | TAC | 96 | a0001c0001t0001g0028 a0001c0001t0001g0129 a0001c0001t0001g0130 others(93): Show |
96 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(93): Show |
intron_variant | MODIFIER | c.459+3069_459+3070d others(4): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 148746822 | ||||||
| chr2:148747132 | T | C | 1 | a0001c0001t0001g0139 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.459+3365T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148747132 | |||||||
| chr2:148747317 | C | A | 5 | a0001c0001t0002g0115 a0001c0001t0002g0116 a0001c0001t0002g0117 others(2): Show |
5 | HG00423.hp2 HG02135.hp2 NA18956.hp2 others(2): Show |
intron_variant | MODIFIER | c.459+3550C>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148747317 | |||||||
| chr2:148747344 | C | T | 107 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(104): Show |
107 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(104): Show |
intron_variant | MODIFIER | c.459+3577C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148747344 | |||||||
| chr2:148747363 | C | A | 9 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(6): Show |
9 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.459+3596C>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148747363 | |||||||
| chr2:148747568 | T | G | 4 | a0001c0001t0002g0099 a0001c0001t0002g0100 a0001c0001t0002g0101 others(1): Show |
4 | NA18947.hp1 NA18952.hp2 NA19064.hp2 others(1): Show |
intron_variant | MODIFIER | c.459+3801T>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148747568 | |||||||
| chr2:148747573 | T | C | 4 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(1): Show |
4 | HG00639.hp2 HG02809.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.459+3806T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148747573 | |||||||
| chr2:148747587 | C | T | 289 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(286): Show |
290 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(287): Show |
intron_variant | MODIFIER | c.459+3820C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148747587 | |||||||
| chr2:148747591 | A | T | 163 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0134 others(160): Show |
164 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(161): Show |
intron_variant | MODIFIER | c.459+3824A>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148747591 | |||||||
| chr2:148747599 | C | T | 1 | a0001c0001t0001g0261 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.459+3832C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148747599 | |||||||
| chr2:148747810 | C | T | 3 | a0001c0001t0001g0036 a0001c0001t0001g0042 a0001c0001t0001g0043 |
3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.459+4043C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148747810 | |||||||
| chr2:148747811 | A | G | 110 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(107): Show |
110 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(107): Show |
intron_variant | MODIFIER | c.459+4044A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148747811 | |||||||
| chr2:148747919 | G | T | 4 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(1): Show |
4 | HG02145.hp1 HG02451.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.459+4152G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148747919 | |||||||
| chr2:148748219 | G | T | 2 | a0001c0001t0002g0106 a0001c0001t0002g0107 |
2 | NA18969.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.459+4452G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148748219 | |||||||
| chr2:148748434 | G | C | 2 | a0001c0001t0001g0198 a0001c0001t0001g0199 |
2 | HG02818.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.459+4667G>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148748434 | |||||||
| chr2:148748484 | T | A | 91 | a0001c0001t0002g0037 a0001c0001t0002g0038 a0001c0001t0002g0040 others(88): Show |
91 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.459+4717T>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148748484 | |||||||
| chr2:148748609 | A | G | 1 | a0001c0001t0001g0163 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.459+4842A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148748609 | |||||||
| chr2:148748730 | CAA | C | 3 | a0001c0001t0001g0250 a0001c0001t0001g0251 a0001c0001t0001g0252 |
3 | HG02572.hp2 HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.459+4965_459+4966d others(4): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 148748730 | ||||||
| chr2:148748741 | C | G | 1 | a0001c0003t0001g0269 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.459+4974C>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148748741 | |||||||
| chr2:148748759 | C | A | 1 | a0001c0001t0001g0264 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.459+4992C>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148748759 | |||||||
| chr2:148748851 | A | G | 3 | a0001c0001t0001g0036 a0001c0001t0001g0042 a0001c0001t0001g0043 |
3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.460-5076A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148748851 | |||||||
| chr2:148748914 | G | C | 108 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(105): Show |
108 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(105): Show |
intron_variant | MODIFIER | c.460-5013G>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148748914 | |||||||
| chr2:148748973 | G | T | 1 | a0001c0001t0001g0229 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.460-4954G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148748973 | |||||||
| chr2:148749026 | T | G | 4 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(1): Show |
4 | HG00639.hp2 HG02809.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.460-4901T>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148749026 | |||||||
| chr2:148749223 | T | C | 2 | a0001c0001t0001g0030 a0001c0001t0001g0031 |
2 | HG02155.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.460-4704T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148749223 | |||||||
| chr2:148749472 | A | G | 1 | a0001c0001t0001g0190 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.460-4455A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148749472 | |||||||
| chr2:148749479 | G | GT | 14 | a0001c0001t0001g0136 a0001c0001t0001g0148 a0001c0001t0001g0151 others(11): Show |
14 | HG02074.hp2 HG02080.hp2 HG02602.hp2 others(11): Show |
intron_variant | MODIFIER | c.460-4435dupT | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 148749479 | ||||||
| chr2:148749479 | GT | G | 9 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0031 others(6): Show |
9 | HG00639.hp2 HG01981.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.460-4435delT | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 148749479 | ||||||
| chr2:148749479 | GTT | G | 9 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0029 others(6): Show |
9 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.460-4436_460-4435d others(4): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 148749479 | ||||||
| chr2:148749493 | C | A | 1 | a0001c0001t0001g0168 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.460-4434C>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148749493 | |||||||
| chr2:148749502 | G | A | 1 | a0001c0001t0001g0306 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.460-4425G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148749502 | |||||||
| chr2:148749625 | G | C | 1 | a0001c0001t0002g0097 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.460-4302G>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148749625 | |||||||
| chr2:148749649 | T | A | 1 | a0001c0001t0002g0066 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.460-4278T>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148749649 | |||||||
| chr2:148749811 | G | A | 3 | a0001c0001t0001g0036 a0001c0001t0001g0042 a0001c0001t0001g0043 |
3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.460-4116G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148749811 | |||||||
| chr2:148749828 | TTA | T | 9 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(6): Show |
9 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.460-4097_460-4096d others(4): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 148749828 | ||||||
| chr2:148749955 | G | A | 1 | a0001c0001t0001g0279 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.460-3972G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148749955 | |||||||
| chr2:148750471 | G | T | 1 | a0001c0001t0001g0304 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.460-3456G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148750471 | |||||||
| chr2:148750519 | T | C | 1 | a0001c0001t0001g0184 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.460-3408T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148750519 | |||||||
| chr2:148750710 | G | T | 1 | a0001c0001t0001g0277 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.460-3217G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148750710 | |||||||
| chr2:148750899 | G | A | 15 | a0001c0001t0001g0289 a0001c0001t0001g0290 a0001c0001t0001g0291 others(12): Show |
15 | HG00673.hp2 HG02074.hp2 NA18949.hp2 others(12): Show |
intron_variant | MODIFIER | c.460-3028G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148750899 | |||||||
| chr2:148750976 | A | T | 111 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0134 others(108): Show |
111 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(108): Show |
intron_variant | MODIFIER | c.460-2951A>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148750976 | |||||||
| chr2:148751245 | G | A | 1 | a0001c0001t0001g0203 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.460-2682G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148751245 | |||||||
| chr2:148751528 | T | C | 1 | a0001c0001t0001g0036 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.460-2399T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148751528 | |||||||
| chr2:148751695 | G | T | 1 | a0001c0001t0001g0015 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.460-2232G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148751695 | |||||||
| chr2:148751763 | A | G | 11 | a0001c0001t0001g0274 a0001c0001t0001g0275 a0001c0001t0001g0276 others(8): Show |
11 | HG02257.hp1 HG02257.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.460-2164A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148751763 | |||||||
| chr2:148751884 | A | G | 9 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(6): Show |
9 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.460-2043A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148751884 | |||||||
| chr2:148752092 | A | G | 107 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(104): Show |
107 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(104): Show |
intron_variant | MODIFIER | c.460-1835A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148752092 | |||||||
| chr2:148752099 | A | G | 4 | a0001c0001t0002g0099 a0001c0001t0002g0100 a0001c0001t0002g0101 others(1): Show |
4 | NA18947.hp1 NA18952.hp2 NA19064.hp2 others(1): Show |
intron_variant | MODIFIER | c.460-1828A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148752099 | |||||||
| chr2:148752163 | A | G | 11 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0178 others(8): Show |
12 | HG00544.hp2 HG00609.hp2 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.460-1764A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148752163 | |||||||
| chr2:148752384 | G | A | 9 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(6): Show |
9 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.460-1543G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148752384 | |||||||
| chr2:148752416 | C | T | 9 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(6): Show |
9 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.460-1511C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148752416 | |||||||
| chr2:148752418 | G | A | 4 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(1): Show |
4 | HG00639.hp2 HG02809.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.460-1509G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148752418 | |||||||
| chr2:148752466 | T | G | 1 | a0001c0001t0002g0133 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.460-1461T>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148752466 | |||||||
| chr2:148752592 | G | A | 1 | a0001c0001t0001g0203 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.460-1335G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148752592 | |||||||
| chr2:148752613 | C | T | 1 | a0001c0001t0002g0114 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.460-1314C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148752613 | |||||||
| chr2:148752713 | G | A | 40 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(37): Show |
40 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.460-1214G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148752713 | |||||||
| chr2:148752733 | A | G | 11 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0178 others(8): Show |
12 | HG00544.hp2 HG00609.hp2 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.460-1194A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148752733 | |||||||
| chr2:148752909 | C | T | 1 | a0001c0001t0001g0195 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.460-1018C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148752909 | |||||||
| chr2:148752943 | T | G | 95 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(92): Show |
95 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.460-984T>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148752943 | |||||||
| chr2:148753113 | T | C | 2 | a0001c0001t0001g0276 a0001c0001t0001g0277 |
2 | HG02615.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.460-814T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148753113 | |||||||
| chr2:148753310 | A | G | 8 | a0001c0001t0001g0289 a0001c0001t0001g0291 a0001c0001t0001g0294 others(5): Show |
8 | HG00673.hp2 NA18949.hp2 NA18959.hp2 others(5): Show |
intron_variant | MODIFIER | c.460-617A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148753310 | |||||||
| chr2:148753497 | G | A | 5 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0191 others(2): Show |
5 | HG02258.hp1 HG02886.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.460-430G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148753497 | |||||||
| chr2:148753597 | CAG | C | 3 | a0001c0001t0001g0036 a0001c0001t0001g0042 a0001c0001t0001g0043 |
3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.460-327_460-326del others(2): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 148753597 | ||||||
| chr2:148753749 | A | G | 3 | a0001c0001t0001g0250 a0001c0001t0001g0251 a0001c0001t0001g0252 |
3 | HG02572.hp2 HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.460-178A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 3/13 | chr2 | 148753749 | |||||||
| chr2:148754142 | C | T | 3 | a0001c0001t0001g0250 a0001c0001t0001g0251 a0001c0001t0001g0252 |
3 | HG02572.hp2 HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.666+9C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 4/13 | chr2 | 148754142 | |||||||
| chr2:148754201 | A | G | 4 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(1): Show |
4 | HG00639.hp2 HG02809.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.666+68A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 4/13 | chr2 | 148754201 | |||||||
| chr2:148754448 | A | T | 111 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(108): Show |
111 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(108): Show |
intron_variant | MODIFIER | c.666+315A>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 4/13 | chr2 | 148754448 | |||||||
| chr2:148754537 | G | A | 2 | a0001c0001t0002g0106 a0001c0001t0002g0107 |
2 | NA18969.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.666+404G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 4/13 | chr2 | 148754537 | |||||||
| chr2:148754844 | T | C | 1 | a0001c0001t0001g0027 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.666+711T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 4/13 | chr2 | 148754844 | |||||||
| chr2:148754888 | T | C | 3 | a0001c0001t0001g0250 a0001c0001t0001g0251 a0001c0001t0001g0252 |
3 | HG02572.hp2 HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.666+755T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 4/13 | chr2 | 148754888 | |||||||
| chr2:148754932 | C | T | 1 | a0001c0001t0001g0306 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.666+799C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 4/13 | chr2 | 148754932 | |||||||
| chr2:148755317 | T | C | 98 | a0001c0001t0001g0036 a0001c0001t0001g0042 a0001c0001t0001g0043 others(95): Show |
98 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(95): Show |
intron_variant | MODIFIER | c.666+1184T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 4/13 | chr2 | 148755317 | |||||||
| chr2:148755510 | C | T | 1 | a0001c0001t0001g0028 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.666+1377C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 4/13 | chr2 | 148755510 | |||||||
| chr2:148755601 | T | G | 20 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0001g0184 others(17): Show |
20 | HG00673.hp2 HG02074.hp2 HG04204.hp1 others(17): Show |
intron_variant | MODIFIER | c.666+1468T>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 4/13 | chr2 | 148755601 | |||||||
| chr2:148755674 | A | G | 1 | a0001c0001t0001g0130 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.666+1541A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 4/13 | chr2 | 148755674 | |||||||
| chr2:148755761 | C | T | 10 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0015 others(7): Show |
10 | HG01891.hp1 HG02258.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.666+1628C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 4/13 | chr2 | 148755761 | |||||||
| chr2:148755910 | T | C | 1 | a0001c0001t0001g0267 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.666+1777T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 4/13 | chr2 | 148755910 | |||||||
| chr2:148755995 | C | A | 1 | a0001c0001t0001g0260 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.666+1862C>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 4/13 | chr2 | 148755995 | |||||||
| chr2:148756317 | A | G | 1 | a0001c0001t0001g0251 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.666+2184A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 4/13 | chr2 | 148756317 | |||||||
| chr2:148756466 | T | G | 4 | a0001c0001t0001g0171 a0001c0001t0001g0241 a0001c0001t0001g0242 others(1): Show |
4 | HG00639.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.666+2333T>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 4/13 | chr2 | 148756466 | |||||||
| chr2:148756541 | C | T | 1 | a0001c0001t0003g0121 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.666+2408C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 4/13 | chr2 | 148756541 | |||||||
| chr2:148756791 | G | A | 91 | a0001c0001t0002g0037 a0001c0001t0002g0038 a0001c0001t0002g0040 others(88): Show |
91 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.666+2658G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 4/13 | chr2 | 148756791 | |||||||
| chr2:148756986 | A | C | 1 | a0001c0005t0001g0186 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.666+2853A>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 4/13 | chr2 | 148756986 | |||||||
| chr2:148757058 | A | T | 4 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(1): Show |
4 | HG00639.hp2 HG02809.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.666+2925A>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 4/13 | chr2 | 148757058 | |||||||
| chr2:148757077 | T | A | 1 | a0001c0001t0002g0088 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.666+2944T>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 4/13 | chr2 | 148757077 | |||||||
| chr2:148757136 | G | A | 3 | a0001c0001t0001g0152 a0001c0001t0001g0161 a0001c0001t0001g0162 |
3 | HG01123.hp1 HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.666+3003G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 4/13 | chr2 | 148757136 | |||||||
| chr2:148757147 | C | T | 1 | a0001c0001t0002g0065 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.666+3014C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 4/13 | chr2 | 148757147 | |||||||
| chr2:148757239 | G | A | 1 | a0001c0001t0001g0278 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.666+3106G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 4/13 | chr2 | 148757239 | |||||||
| chr2:148757325 | G | A | 12 | a0001c0001t0001g0171 a0001c0001t0001g0189 a0001c0001t0001g0190 others(9): Show |
12 | HG00639.hp1 HG02109.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.666+3192G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 4/13 | chr2 | 148757325 | |||||||
| chr2:148757352 | G | T | 4 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(1): Show |
4 | HG00639.hp2 HG02809.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.666+3219G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 4/13 | chr2 | 148757352 | |||||||
| chr2:148757562 | G | C | 1 | a0001c0001t0001g0238 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.666+3429G>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 4/13 | chr2 | 148757562 | |||||||
| chr2:148757791 | C | T | 1 | a0001c0001t0001g0214 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.666+3658C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 4/13 | chr2 | 148757791 | |||||||
| chr2:148757795 | A | G | 91 | a0001c0001t0002g0037 a0001c0001t0002g0038 a0001c0001t0002g0040 others(88): Show |
91 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.666+3662A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 4/13 | chr2 | 148757795 | |||||||
| chr2:148757862 | A | G | 1 | a0001c0001t0002g0133 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.666+3729A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 4/13 | chr2 | 148757862 | |||||||
| chr2:148757945 | G | T | 1 | a0002c0002t0006g0254 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.666+3812G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 4/13 | chr2 | 148757945 | |||||||
| chr2:148757982 | G | T | 110 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(107): Show |
110 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(107): Show |
intron_variant | MODIFIER | c.667-3800G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 4/13 | chr2 | 148757982 | |||||||
| chr2:148758084 | G | A | 1 | a0001c0005t0001g0009 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.667-3698G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 4/13 | chr2 | 148758084 | |||||||
| chr2:148758154 | A | G | 91 | a0001c0001t0002g0037 a0001c0001t0002g0038 a0001c0001t0002g0040 others(88): Show |
91 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.667-3628A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 4/13 | chr2 | 148758154 | |||||||
| chr2:148758159 | T | TGTGG | 4 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(1): Show |
4 | HG00639.hp2 HG02809.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.667-3607_667-3604d others(6): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 148758159 | ||||||
| chr2:148758162 | G | C | 1 | a0001c0001t0001g0043 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.667-3620G>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 4/13 | chr2 | 148758162 | |||||||
| chr2:148758197 | G | A | 3 | a0001c0001t0001g0036 a0001c0001t0001g0042 a0001c0001t0001g0043 |
3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.667-3585G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 4/13 | chr2 | 148758197 | |||||||
| chr2:148758207 | A | G | 2 | a0001c0001t0001g0258 a0001c0001t0001g0259 |
2 | HG00280.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.667-3575A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 4/13 | chr2 | 148758207 | |||||||
| chr2:148758343 | A | T | 1 | a0001c0001t0001g0267 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.667-3439A>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 4/13 | chr2 | 148758343 | |||||||
| chr2:148758398 | A | T | 159 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(156): Show |
160 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(157): Show |
intron_variant | MODIFIER | c.667-3384A>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 4/13 | chr2 | 148758398 | |||||||
| chr2:148758464 | C | T | 1 | a0001c0001t0002g0052 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.667-3318C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 4/13 | chr2 | 148758464 | |||||||
| chr2:148758527 | C | T | 4 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(1): Show |
4 | HG02145.hp1 HG02451.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.667-3255C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 4/13 | chr2 | 148758527 | |||||||
| chr2:148758642 | C | T | 4 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(1): Show |
4 | HG00639.hp2 HG02809.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.667-3140C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 4/13 | chr2 | 148758642 | |||||||
| chr2:148759252 | C | T | 9 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(6): Show |
9 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.667-2530C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 4/13 | chr2 | 148759252 | |||||||
| chr2:148759284 | G | C | 3 | a0001c0001t0001g0250 a0001c0001t0001g0251 a0001c0001t0001g0252 |
3 | HG02572.hp2 HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.667-2498G>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 4/13 | chr2 | 148759284 | |||||||
| chr2:148759386 | C | T | 3 | a0001c0001t0002g0037 a0001c0001t0002g0046 a0001c0001t0002g0048 |
3 | HG01069.hp1 HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.667-2396C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 4/13 | chr2 | 148759386 | |||||||
| chr2:148759388 | C | T | 1 | a0001c0001t0002g0044 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.667-2394C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 4/13 | chr2 | 148759388 | |||||||
| chr2:148759389 | G | A | 4 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(1): Show |
4 | HG02145.hp1 HG02451.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.667-2393G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 4/13 | chr2 | 148759389 | |||||||
| chr2:148759605 | G | T | 1 | a0001c0001t0002g0049 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.667-2177G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 4/13 | chr2 | 148759605 | |||||||
| chr2:148759799 | T | C | 11 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0178 others(8): Show |
12 | HG00544.hp2 HG00609.hp2 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.667-1983T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 4/13 | chr2 | 148759799 | |||||||
| chr2:148759886 | T | C | 1 | a0001c0001t0001g0306 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.667-1896T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 4/13 | chr2 | 148759886 | |||||||
| chr2:148759887 | G | C | 1 | a0001c0001t0001g0306 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.667-1895G>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 4/13 | chr2 | 148759887 | |||||||
| chr2:148759973 | TGG | T | 4 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(1): Show |
4 | HG00639.hp2 HG02809.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.667-1808_667-1807d others(4): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 4/13 | chr2 | 148759973 | |||||||
| chr2:148760072 | A | G | 91 | a0001c0001t0002g0037 a0001c0001t0002g0038 a0001c0001t0002g0040 others(88): Show |
91 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.667-1710A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 4/13 | chr2 | 148760072 | |||||||
| chr2:148760123 | A | C | 4 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(1): Show |
4 | HG00639.hp2 HG02809.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.667-1659A>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 4/13 | chr2 | 148760123 | |||||||
| chr2:148760171 | C | T | 2 | a0001c0001t0001g0201 a0001c0001t0001g0213 |
2 | HG01346.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.667-1611C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 4/13 | chr2 | 148760171 | |||||||
| chr2:148760183 | G | T | 1 | a0001c0001t0001g0306 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.667-1599G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 4/13 | chr2 | 148760183 | |||||||
| chr2:148760307 | C | T | 2 | a0001c0001t0001g0292 a0001c0001t0001g0295 |
2 | NA18960.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.667-1475C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 4/13 | chr2 | 148760307 | |||||||
| chr2:148760318 | C | A | 1 | a0001c0001t0001g0199 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.667-1464C>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 4/13 | chr2 | 148760318 | |||||||
| chr2:148760371 | C | T | 3 | a0001c0001t0001g0148 a0001c0001t0001g0150 a0001c0001t0001g0154 |
3 | NA19005.hp2 NA19064.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.667-1411C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 4/13 | chr2 | 148760371 | |||||||
| chr2:148760483 | G | A | 3 | a0001c0001t0001g0036 a0001c0001t0001g0042 a0001c0001t0001g0043 |
3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.667-1299G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 4/13 | chr2 | 148760483 | |||||||
| chr2:148761232 | C | T | 9 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(6): Show |
9 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.667-550C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 4/13 | chr2 | 148761232 | |||||||
| chr2:148761380 | G | T | 1 | a0001c0001t0001g0252 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.667-402G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 4/13 | chr2 | 148761380 | |||||||
| chr2:148761392 | C | T | 9 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(6): Show |
9 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.667-390C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 4/13 | chr2 | 148761392 | |||||||
| chr2:148761439 | T | G | 1 | a0001c0001t0001g0195 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.667-343T>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 4/13 | chr2 | 148761439 | |||||||
| chr2:148761660 | C | T | 1 | a0001c0005t0001g0186 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.667-122C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 4/13 | chr2 | 148761660 | |||||||
| chr2:148761729 | G | A | 3 | a0001c0001t0001g0250 a0001c0001t0001g0251 a0001c0001t0001g0252 |
3 | HG02572.hp2 HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.667-53G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 4/13 | chr2 | 148761729 | |||||||
| chr2:148761998 | G | T | 1 | a0001c0001t0001g0212 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.815+68G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 5/13 | chr2 | 148761998 | |||||||
| chr2:148762089 | T | C | 1 | a0001c0001t0001g0234 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.815+159T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 5/13 | chr2 | 148762089 | |||||||
| chr2:148762443 | G | A | 4 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(1): Show |
4 | HG02145.hp1 HG02451.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.816-227G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 5/13 | chr2 | 148762443 | |||||||
| chr2:148762490 | G | A | 9 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(6): Show |
9 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.816-180G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 5/13 | chr2 | 148762490 | |||||||
| chr2:148762617 | T | C | 40 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(37): Show |
40 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.816-53T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 5/13 | chr2 | 148762617 | |||||||
| chr2:148762645 | C | A | 124 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0134 others(121): Show |
124 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(121): Show |
intron_variant | MODIFIER | c.816-25C>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 5/13 | chr2 | 148762645 | |||||||
| chr2:148762911 | G | C | 1 | a0001c0001t0001g0028 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.948+109G>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 6/13 | chr2 | 148762911 | |||||||
| chr2:148762969 | G | A | 2 | a0001c0001t0001g0010 a0001c0001t0001g0029 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.948+167G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 6/13 | chr2 | 148762969 | |||||||
| chr2:148763313 | T | G | 1 | a0002c0002t0001g0253 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.948+511T>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 6/13 | chr2 | 148763313 | |||||||
| chr2:148763510 | C | CT | 5 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0001c0003t0001g0249 others(2): Show |
5 | HG01884.hp1 HG02109.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.948+711dupT | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | 148763510 | ||||||
| chr2:148763528 | T | A | 1 | a0001c0001t0001g0250 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.948+726T>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 6/13 | chr2 | 148763528 | |||||||
| chr2:148763749 | C | T | 1 | a0001c0001t0001g0031 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.948+947C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 6/13 | chr2 | 148763749 | |||||||
| chr2:148763811 | A | G | 1 | a0001c0003t0001g0269 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.948+1009A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 6/13 | chr2 | 148763811 | |||||||
| chr2:148764028 | A | G | 3 | a0001c0001t0001g0137 a0001c0001t0001g0158 a0001c0001t0001g0159 |
3 | NA18969.hp1 NA19001.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.949-927A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 6/13 | chr2 | 148764028 | |||||||
| chr2:148764280 | C | T | 4 | a0001c0001t0001g0294 a0001c0001t0001g0299 a0001c0001t0001g0300 others(1): Show |
4 | NA18959.hp2 NA18998.hp2 NA19057.hp1 others(1): Show |
intron_variant | MODIFIER | c.949-675C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 6/13 | chr2 | 148764280 | |||||||
| chr2:148764292 | A | G | 91 | a0001c0001t0002g0037 a0001c0001t0002g0038 a0001c0001t0002g0040 others(88): Show |
91 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.949-663A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 6/13 | chr2 | 148764292 | |||||||
| chr2:148764607 | ATAG | A | 3 | a0001c0001t0001g0036 a0001c0001t0001g0042 a0001c0001t0001g0043 |
3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.949-346_949-344del others(3): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | 148764607 | ||||||
| chr2:148764721 | G | A | 2 | a0001c0001t0001g0236 a0001c0001t0001g0237 |
2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.949-234G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 6/13 | chr2 | 148764721 | |||||||
| chr2:148764756 | CA | C | 8 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0015 others(5): Show |
8 | HG02258.hp2 HG02717.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.949-198delA | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 6/13 | chr2 | 148764756 | |||||||
| chr2:148764794 | A | G | 2 | a0001c0001t0002g0106 a0001c0001t0002g0107 |
2 | NA18969.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.949-161A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 6/13 | chr2 | 148764794 | |||||||
| chr2:148764827 | C | T | 1 | a0001c0001t0002g0093 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.949-128C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 6/13 | chr2 | 148764827 | |||||||
| chr2:148764828 | G | A | 5 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0202 others(2): Show |
5 | NA18985.hp2 NA19006.hp1 NA19077.hp1 others(2): Show |
intron_variant | MODIFIER | c.949-127G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 6/13 | chr2 | 148764828 | |||||||
| chr2:148765280 | G | T | 107 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(104): Show |
107 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(104): Show |
intron_variant | MODIFIER | c.1140+134G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 7/13 | chr2 | 148765280 | |||||||
| chr2:148765380 | T | C | 1 | a0001c0001t0001g0170 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1140+234T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 7/13 | chr2 | 148765380 | |||||||
| chr2:148765493 | G | T | 4 | a0001c0001t0001g0271 a0001c0003t0001g0249 a0001c0003t0001g0269 others(1): Show |
4 | HG01884.hp1 HG02109.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.1140+347G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 7/13 | chr2 | 148765493 | |||||||
| chr2:148765798 | G | A | 1 | a0001c0001t0001g0136 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1140+652G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 7/13 | chr2 | 148765798 | |||||||
| chr2:148765823 | A | G | 290 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(287): Show |
291 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(288): Show |
intron_variant | MODIFIER | c.1140+677A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 7/13 | chr2 | 148765823 | |||||||
| chr2:148765887 | TC | T | 91 | a0001c0001t0002g0037 a0001c0001t0002g0038 a0001c0001t0002g0040 others(88): Show |
91 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.1140+742delC | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 7/13 | chr2 | 148765887 | |||||||
| chr2:148765908 | C | T | 4 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(1): Show |
4 | HG00639.hp2 HG02809.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1140+762C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 7/13 | chr2 | 148765908 | |||||||
| chr2:148765918 | C | T | 11 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0178 others(8): Show |
12 | HG00544.hp2 HG00609.hp2 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.1140+772C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 7/13 | chr2 | 148765918 | |||||||
| chr2:148765973 | T | G | 1 | a0001c0001t0002g0087 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1140+827T>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 7/13 | chr2 | 148765973 | |||||||
| chr2:148766078 | A | G | 2 | a0001c0001t0001g0140 a0001c0001t0001g0167 |
2 | NA18941.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.1140+932A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 7/13 | chr2 | 148766078 | |||||||
| chr2:148766129 | G | A | 107 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(104): Show |
107 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(104): Show |
intron_variant | MODIFIER | c.1140+983G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 7/13 | chr2 | 148766129 | |||||||
| chr2:148766524 | T | G | 9 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(6): Show |
9 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.1140+1378T>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 7/13 | chr2 | 148766524 | |||||||
| chr2:148766552 | T | G | 107 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(104): Show |
107 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(104): Show |
intron_variant | MODIFIER | c.1140+1406T>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 7/13 | chr2 | 148766552 | |||||||
| chr2:148766610 | A | G | 5 | a0001c0001t0001g0274 a0001c0001t0001g0275 a0001c0001t0001g0276 others(2): Show |
5 | HG02572.hp1 HG02615.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1140+1464A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 7/13 | chr2 | 148766610 | |||||||
| chr2:148766715 | C | T | 1 | a0001c0001t0001g0189 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1140+1569C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 7/13 | chr2 | 148766715 | |||||||
| chr2:148766757 | T | C | 2 | a0001c0001t0001g0251 a0001c0001t0001g0252 |
2 | HG02572.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1140+1611T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 7/13 | chr2 | 148766757 | |||||||
| chr2:148766840 | G | T | 1 | a0001c0001t0001g0250 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1140+1694G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 7/13 | chr2 | 148766840 | |||||||
| chr2:148766925 | T | C | 1 | a0001c0001t0001g0185 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.1140+1779T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 7/13 | chr2 | 148766925 | |||||||
| chr2:148766950 | G | A | 159 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0134 others(156): Show |
160 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(157): Show |
intron_variant | MODIFIER | c.1140+1804G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 7/13 | chr2 | 148766950 | |||||||
| chr2:148766976 | G | T | 1 | a0001c0005t0001g0009 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1140+1830G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 7/13 | chr2 | 148766976 | |||||||
| chr2:148767038 | A | G | 1 | a0001c0001t0001g0195 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1140+1892A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 7/13 | chr2 | 148767038 | |||||||
| chr2:148767128 | A | G | 11 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0178 others(8): Show |
12 | HG00544.hp2 HG00609.hp2 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.1140+1982A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 7/13 | chr2 | 148767128 | |||||||
| chr2:148767139 | T | A | 290 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(287): Show |
291 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(288): Show |
intron_variant | MODIFIER | c.1140+1993T>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 7/13 | chr2 | 148767139 | |||||||
| chr2:148767197 | CA | C | 160 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(157): Show |
161 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(158): Show |
intron_variant | MODIFIER | c.1141-1936delA | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr2 | 148767197 | ||||||
| chr2:148767197 | CAA | C | 29 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(26): Show |
29 | HG00673.hp2 HG02040.hp2 HG02074.hp2 others(26): Show |
intron_variant | MODIFIER | c.1141-1937_1141-193 others(6): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr2 | 148767197 | ||||||
| chr2:148767285 | A | G | 1 | a0001c0001t0001g0272 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1141-1866A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 7/13 | chr2 | 148767285 | |||||||
| chr2:148767383 | T | C | 95 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(92): Show |
95 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.1141-1768T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 7/13 | chr2 | 148767383 | |||||||
| chr2:148767419 | T | C | 1 | a0001c0001t0002g0124 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1141-1732T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 7/13 | chr2 | 148767419 | |||||||
| chr2:148767439 | G | C | 10 | a0001c0001t0001g0171 a0001c0001t0001g0189 a0001c0001t0001g0190 others(7): Show |
10 | HG00639.hp1 HG02109.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.1141-1712G>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 7/13 | chr2 | 148767439 | |||||||
| chr2:148767461 | C | T | 1 | a0001c0001t0001g0008 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1141-1690C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 7/13 | chr2 | 148767461 | |||||||
| chr2:148767592 | C | A | 1 | a0001c0001t0001g0149 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1141-1559C>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 7/13 | chr2 | 148767592 | |||||||
| chr2:148767658 | A | G | 1 | a0001c0001t0002g0060 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1141-1493A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 7/13 | chr2 | 148767658 | |||||||
| chr2:148768320 | C | G | 1 | a0002c0002t0006g0254 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1141-831C>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 7/13 | chr2 | 148768320 | |||||||
| chr2:148768378 | C | T | 4 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(1): Show |
4 | HG02145.hp1 HG02451.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1141-773C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 7/13 | chr2 | 148768378 | |||||||
| chr2:148768426 | G | A | 1 | a0001c0001t0001g0165 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1141-725G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 7/13 | chr2 | 148768426 | |||||||
| chr2:148768564 | A | T | 110 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(107): Show |
110 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(107): Show |
intron_variant | MODIFIER | c.1141-587A>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 7/13 | chr2 | 148768564 | |||||||
| chr2:148768645 | T | C | 3 | a0001c0001t0001g0036 a0001c0001t0001g0042 a0001c0001t0001g0043 |
3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1141-506T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 7/13 | chr2 | 148768645 | |||||||
| chr2:148768682 | T | A | 1 | a0001c0001t0002g0069 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1141-469T>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 7/13 | chr2 | 148768682 | |||||||
| chr2:148768892 | T | A | 9 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(6): Show |
9 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.1141-259T>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 7/13 | chr2 | 148768892 | |||||||
| chr2:148768986 | A | G | 2 | a0001c0001t0001g0251 a0001c0001t0001g0252 |
2 | HG02572.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1141-165A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 7/13 | chr2 | 148768986 | |||||||
| chr2:148769759 | T | C | 1 | a0001c0001t0001g0194 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1230+519T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 8/13 | chr2 | 148769759 | |||||||
| chr2:148769895 | G | A | 2 | a0001c0001t0002g0103 a0001c0001t0002g0109 |
2 | HG02523.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.1230+655G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 8/13 | chr2 | 148769895 | |||||||
| chr2:148769960 | C | T | 1 | a0001c0001t0001g0306 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1230+720C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 8/13 | chr2 | 148769960 | |||||||
| chr2:148770293 | G | A | 1 | a0002c0002t0001g0253 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1231-499G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 8/13 | chr2 | 148770293 | |||||||
| chr2:148770294 | C | A | 1 | a0002c0002t0001g0253 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1231-498C>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 8/13 | chr2 | 148770294 | |||||||
| chr2:148770305 | G | A | 12 | a0001c0001t0001g0171 a0001c0001t0001g0189 a0001c0001t0001g0190 others(9): Show |
12 | HG00639.hp1 HG02109.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.1231-487G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 8/13 | chr2 | 148770305 | |||||||
| chr2:148770332 | A | C | 1 | a0001c0001t0002g0063 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1231-460A>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 8/13 | chr2 | 148770332 | |||||||
| chr2:148770395 | T | C | 7 | a0001c0001t0001g0036 a0001c0001t0001g0042 a0001c0001t0001g0043 others(4): Show |
7 | HG00639.hp2 HG02145.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1231-397T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 8/13 | chr2 | 148770395 | |||||||
| chr2:148770419 | AATAT | A | 9 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(6): Show |
9 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.1231-372_1231-369d others(6): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 8/13 | chr2 | 148770419 | |||||||
| chr2:148770565 | T | G | 2 | a0001c0004t0001g0013 a0001c0004t0001g0026 |
2 | HG01891.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1231-227T>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 8/13 | chr2 | 148770565 | |||||||
| chr2:148770594 | G | C | 5 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0001c0003t0001g0249 others(2): Show |
5 | HG01884.hp1 HG02109.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1231-198G>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 8/13 | chr2 | 148770594 | |||||||
| chr2:148770608 | T | C | 1 | a0001c0001t0001g0170 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1231-184T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 8/13 | chr2 | 148770608 | |||||||
| chr2:148770626 | T | A | 1 | a0001c0001t0001g0238 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1231-166T>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 8/13 | chr2 | 148770626 | |||||||
| chr2:148770651 | G | A | 3 | a0001c0001t0001g0250 a0001c0001t0001g0251 a0001c0001t0001g0252 |
3 | HG02572.hp2 HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1231-141G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 8/13 | chr2 | 148770651 | |||||||
| chr2:148771514 | T | C | 289 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(286): Show |
290 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(287): Show |
intron_variant | MODIFIER | c.1720+127T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148771514 | |||||||
| chr2:148771526 | A | G | 91 | a0001c0001t0002g0037 a0001c0001t0002g0038 a0001c0001t0002g0040 others(88): Show |
91 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.1720+139A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148771526 | |||||||
| chr2:148771618 | TC | T | 9 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(6): Show |
9 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.1720+234delC | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr2 | 148771618 | ||||||
| chr2:148771643 | C | T | 94 | a0001c0001t0001g0036 a0001c0001t0001g0042 a0001c0001t0001g0043 others(91): Show |
94 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(91): Show |
intron_variant | MODIFIER | c.1720+256C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148771643 | |||||||
| chr2:148771802 | A | AT | 113 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(110): Show |
113 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(110): Show |
intron_variant | MODIFIER | c.1720+430dupT | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr2 | 148771802 | ||||||
| chr2:148771922 | C | G | 2 | a0001c0001t0001g0198 a0001c0001t0001g0199 |
2 | HG02818.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1720+535C>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148771922 | |||||||
| chr2:148771925 | A | G | 4 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(1): Show |
4 | HG02145.hp1 HG02451.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1720+538A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148771925 | |||||||
| chr2:148772095 | G | A | 5 | a0001c0001t0001g0274 a0001c0001t0001g0275 a0001c0001t0001g0276 others(2): Show |
5 | HG02572.hp1 HG02615.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1720+708G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148772095 | |||||||
| chr2:148772373 | C | A | 13 | a0001c0001t0001g0137 a0001c0001t0001g0140 a0001c0001t0001g0155 others(10): Show |
13 | HG02135.hp1 NA18747.hp1 NA18941.hp1 others(10): Show |
intron_variant | MODIFIER | c.1720+986C>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148772373 | |||||||
| chr2:148772427 | G | C | 129 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0134 others(126): Show |
129 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(126): Show |
intron_variant | MODIFIER | c.1720+1040G>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148772427 | |||||||
| chr2:148772808 | C | A | 1 | a0001c0001t0008g0039 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1720+1421C>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148772808 | |||||||
| chr2:148772810 | A | T | 1 | a0001c0001t0008g0039 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1720+1423A>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148772810 | |||||||
| chr2:148772811 | A | T | 1 | a0001c0001t0008g0039 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1720+1424A>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148772811 | |||||||
| chr2:148773034 | C | T | 16 | a0001c0001t0001g0196 a0001c0001t0001g0200 a0001c0001t0001g0204 others(13): Show |
16 | HG01256.hp2 HG01433.hp1 HG01943.hp2 others(13): Show |
intron_variant | MODIFIER | c.1720+1647C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148773034 | |||||||
| chr2:148773092 | T | C | 34 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0178 others(31): Show |
35 | HG00544.hp2 HG00609.hp2 HG00673.hp2 others(32): Show |
intron_variant | MODIFIER | c.1720+1705T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148773092 | |||||||
| chr2:148773101 | C | T | 1 | a0001c0001t0002g0070 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1720+1714C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148773101 | |||||||
| chr2:148773254 | A | ATTTAT | 7 | a0001c0001t0001g0036 a0001c0001t0001g0042 a0001c0001t0001g0043 others(4): Show |
7 | HG00639.hp2 HG02145.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1720+1871_1720+187 others(9): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr2 | 148773254 | ||||||
| chr2:148773271 | A | AGGC | 3 | a0001c0001t0001g0250 a0001c0001t0001g0251 a0001c0001t0001g0252 |
3 | HG02572.hp2 HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1720+1886_1720+188 others(7): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr2 | 148773271 | ||||||
| chr2:148773275 | G | A | 9 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(6): Show |
9 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.1720+1888G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148773275 | |||||||
| chr2:148773621 | T | C | 1 | a0001c0001t0002g0078 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1720+2234T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148773621 | |||||||
| chr2:148773783 | T | C | 1 | a0001c0001t0001g0304 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1720+2396T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148773783 | |||||||
| chr2:148774246 | T | C | 1 | a0001c0001t0001g0271 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1720+2859T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148774246 | |||||||
| chr2:148774349 | G | A | 2 | a0001c0001t0002g0099 a0001c0001t0002g0100 |
2 | NA19064.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.1720+2962G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148774349 | |||||||
| chr2:148774438 | G | A | 1 | a0001c0001t0001g0036 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1720+3051G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148774438 | |||||||
| chr2:148774614 | A | T | 5 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(2): Show |
5 | HG02145.hp2 HG02895.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1720+3227A>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148774614 | |||||||
| chr2:148774616 | A | T | 112 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(109): Show |
112 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(109): Show |
intron_variant | MODIFIER | c.1720+3229A>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148774616 | |||||||
| chr2:148774622 | T | TTATATAT others(17): Show |
1 | a0001c0001t0001g0043 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1720+3236_1720+323 others(28): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr2 | 148774622 | ||||||
| chr2:148774622 | T | TTATATAT others(21): Show |
1 | a0001c0001t0001g0036 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1720+3236_1720+323 others(32): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr2 | 148774622 | ||||||
| chr2:148774622 | T | TTATATAT others(23): Show |
1 | a0001c0001t0001g0042 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1720+3236_1720+323 others(34): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr2 | 148774622 | ||||||
| chr2:148774622 | T | TTATATTA others(12): Show |
6 | a0001c0001t0002g0055 a0001c0001t0002g0056 a0001c0001t0002g0057 others(3): Show |
6 | HG01106.hp1 HG01515.hp1 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.1720+3236_1720+323 others(23): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr2 | 148774622 | ||||||
| chr2:148774622 | T | TTATATTA others(14): Show |
31 | a0001c0001t0002g0044 a0001c0001t0002g0053 a0001c0001t0002g0054 others(28): Show |
31 | HG00642.hp2 HG00735.hp1 HG00741.hp1 others(28): Show |
intron_variant | MODIFIER | c.1720+3236_1720+323 others(25): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr2 | 148774622 | ||||||
| chr2:148774622 | T | TTATATTA others(16): Show |
14 | a0001c0001t0002g0038 a0001c0001t0002g0065 a0001c0001t0002g0067 others(11): Show |
14 | HG01496.hp1 HG01884.hp2 HG02040.hp1 others(11): Show |
intron_variant | MODIFIER | c.1720+3236_1720+323 others(27): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr2 | 148774622 | ||||||
| chr2:148774622 | T | TTATATTA others(18): Show |
17 | a0001c0001t0002g0037 a0001c0001t0002g0041 a0001c0001t0002g0045 others(14): Show |
17 | HG00280.hp2 HG00738.hp2 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.1720+3236_1720+323 others(29): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr2 | 148774622 | ||||||
| chr2:148774622 | T | TTATATTA others(20): Show |
9 | a0001c0001t0002g0049 a0001c0001t0002g0060 a0001c0001t0002g0063 others(6): Show |
9 | HG00558.hp2 HG00673.hp1 HG01346.hp1 others(6): Show |
intron_variant | MODIFIER | c.1720+3236_1720+323 others(31): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr2 | 148774622 | ||||||
| chr2:148774622 | T | TTATATTA others(22): Show |
5 | a0001c0001t0002g0058 a0001c0001t0002g0102 a0001c0001t0002g0115 others(2): Show |
5 | NA18952.hp2 NA18959.hp1 NA18964.hp2 others(2): Show |
intron_variant | MODIFIER | c.1720+3236_1720+323 others(33): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr2 | 148774622 | ||||||
| chr2:148774622 | T | TTATATTA others(24): Show |
3 | a0001c0001t0002g0047 a0001c0001t0002g0085 a0001c0001t0002g0116 |
3 | HG00423.hp2 HG01943.hp1 HG02071.hp2 |
intron_variant | MODIFIER | c.1720+3236_1720+323 others(35): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr2 | 148774622 | ||||||
| chr2:148774622 | T | TTATATTA others(26): Show |
3 | a0001c0001t0002g0040 a0001c0001t0002g0075 a0001c0001t0002g0081 |
3 | NA18950.hp2 NA19068.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.1720+3236_1720+323 others(37): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr2 | 148774622 | ||||||
| chr2:148774622 | T | TTATATTA others(30): Show |
1 | a0001c0001t0002g0119 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1720+3236_1720+323 others(41): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr2 | 148774622 | ||||||
| chr2:148774622 | T | TTATATTT others(12): Show |
4 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(1): Show |
4 | HG00639.hp2 HG02809.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1720+3236_1720+323 others(23): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr2 | 148774622 | ||||||
| chr2:148774623 | T | TAA | 9 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(6): Show |
9 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.1720+3236_1720+323 others(6): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148774623 | |||||||
| chr2:148774624 | T | A | 100 | a0001c0001t0001g0036 a0001c0001t0001g0042 a0001c0001t0001g0043 others(97): Show |
100 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.1720+3237T>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148774624 | |||||||
| chr2:148774624 | T | TTA | 24 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(21): Show |
24 | HG00673.hp2 HG02074.hp2 HG02145.hp1 others(21): Show |
intron_variant | MODIFIER | c.1720+3253_1720+325 others(6): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr2 | 148774624 | ||||||
| chr2:148774640 | A | ATATATAT others(12): Show |
1 | a0001c0001t0002g0052 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1720+3254_1720+325 others(23): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr2 | 148774640 | ||||||
| chr2:148774853 | C | T | 9 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(6): Show |
9 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.1720+3466C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148774853 | |||||||
| chr2:148774903 | C | T | 3 | a0001c0001t0001g0250 a0001c0001t0001g0251 a0001c0001t0001g0252 |
3 | HG02572.hp2 HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1720+3516C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148774903 | |||||||
| chr2:148774961 | C | T | 1 | a0001c0001t0001g0215 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1720+3574C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148774961 | |||||||
| chr2:148774992 | G | A | 14 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0178 others(11): Show |
15 | HG00544.hp2 HG00609.hp2 HG01106.hp2 others(12): Show |
intron_variant | MODIFIER | c.1720+3605G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148774992 | |||||||
| chr2:148775006 | G | T | 3 | a0001c0001t0001g0036 a0001c0001t0001g0042 a0001c0001t0001g0043 |
3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1720+3619G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148775006 | |||||||
| chr2:148775088 | CA | C | 180 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(177): Show |
181 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(178): Show |
intron_variant | MODIFIER | c.1720+3717delA | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr2 | 148775088 | ||||||
| chr2:148775088 | CAAA | C | 105 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(102): Show |
105 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(102): Show |
intron_variant | MODIFIER | c.1720+3715_1720+371 others(7): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr2 | 148775088 | ||||||
| chr2:148775135 | G | A | 1 | a0001c0001t0002g0104 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1720+3748G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148775135 | |||||||
| chr2:148775228 | T | C | 91 | a0001c0001t0002g0037 a0001c0001t0002g0038 a0001c0001t0002g0040 others(88): Show |
91 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.1720+3841T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148775228 | |||||||
| chr2:148775340 | G | A | 9 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(6): Show |
9 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.1720+3953G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148775340 | |||||||
| chr2:148775522 | C | A | 1 | a0001c0001t0001g0005 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1720+4135C>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148775522 | |||||||
| chr2:148775606 | A | G | 9 | a0001c0001t0001g0187 a0001c0001t0001g0194 a0001c0001t0001g0231 others(6): Show |
9 | HG01891.hp2 HG02622.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.1720+4219A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148775606 | |||||||
| chr2:148775650 | T | TTTAAATA others(28): Show |
102 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(99): Show |
102 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(99): Show |
intron_variant | MODIFIER | c.1720+4281_1720+431 others(39): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr2 | 148775650 | ||||||
| chr2:148775650 | T | TTTAAATA others(63): Show |
1 | a0001c0001t0002g0114 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1720+4315_1720+431 others(74): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr2 | 148775650 | ||||||
| chr2:148775658 | A | AAATTAAA others(13): Show |
1 | a0001c0001t0001g0194 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1720+4276_1720+429 others(24): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr2 | 148775658 | ||||||
| chr2:148775658 | A | AAATTAAA others(18): Show |
163 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(160): Show |
164 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(161): Show |
intron_variant | MODIFIER | c.1720+4290_1720+431 others(29): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr2 | 148775658 | ||||||
| chr2:148775658 | A | AAATTAAA others(53): Show |
1 | a0001c0001t0001g0166 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1720+4315_1720+431 others(64): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr2 | 148775658 | ||||||
| chr2:148775658 | A | AAATTAAA others(43): Show |
20 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0015 others(17): Show |
20 | HG01891.hp1 HG02135.hp1 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.1720+4314_1720+431 others(54): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr2 | 148775658 | ||||||
| chr2:148775658 | A | AAATTAAA others(18): Show |
1 | a0001c0001t0001g0275 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1720+4279_1720+428 others(29): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr2 | 148775658 | ||||||
| chr2:148775658 | A | AAATTAAA others(8): Show |
3 | a0001c0001t0001g0250 a0001c0001t0001g0251 a0001c0001t0001g0252 |
3 | HG02572.hp2 HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1720+4279_1720+428 others(19): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr2 | 148775658 | ||||||
| chr2:148775700 | A | ATT | 5 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(2): Show |
5 | HG00639.hp2 HG02809.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1720+4314_1720+431 others(6): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr2 | 148775700 | ||||||
| chr2:148775703 | T | A | 5 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(2): Show |
5 | HG00639.hp2 HG02809.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1720+4316T>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148775703 | |||||||
| chr2:148775704 | C | T | 5 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(2): Show |
5 | HG00639.hp2 HG02809.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1720+4317C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148775704 | |||||||
| chr2:148775707 | T | A | 5 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(2): Show |
5 | HG00639.hp2 HG02809.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1720+4320T>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148775707 | |||||||
| chr2:148775714 | TAA | T | 5 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(2): Show |
5 | HG00639.hp2 HG02809.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1720+4332_1720+433 others(6): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr2 | 148775714 | ||||||
| chr2:148775730 | T | TTTATTAA others(8): Show |
1 | a0001c0001t0001g0137 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1720+4346_1720+434 others(19): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr2 | 148775730 | ||||||
| chr2:148775749 | T | G | 1 | a0001c0001t0001g0277 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1720+4362T>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148775749 | |||||||
| chr2:148775775 | C | CT | 128 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(125): Show |
128 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(125): Show |
intron_variant | MODIFIER | c.1720+4408dupT | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr2 | 148775775 | ||||||
| chr2:148775775 | C | CTT | 12 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0143 others(9): Show |
12 | HG00280.hp1 HG00738.hp1 HG01070.hp1 others(9): Show |
intron_variant | MODIFIER | c.1720+4407_1720+440 others(6): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr2 | 148775775 | ||||||
| chr2:148775775 | C | CTTTTT | 8 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(5): Show |
8 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(5): Show |
intron_variant | MODIFIER | c.1720+4404_1720+440 others(9): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr2 | 148775775 | ||||||
| chr2:148775775 | CT | C | 14 | a0001c0001t0001g0028 a0001c0001t0001g0036 a0001c0001t0001g0042 others(11): Show |
14 | HG02145.hp2 HG02257.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.1720+4408delT | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr2 | 148775775 | ||||||
| chr2:148775804 | G | C | 2 | a0001c0001t0001g0198 a0001c0001t0001g0199 |
2 | HG02818.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1720+4417G>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148775804 | |||||||
| chr2:148775831 | A | G | 1 | a0001c0001t0002g0109 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1720+4444A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148775831 | |||||||
| chr2:148775840 | C | T | 1 | a0001c0001t0001g0259 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1720+4453C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148775840 | |||||||
| chr2:148775851 | C | T | 1 | a0001c0001t0002g0064 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1720+4464C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148775851 | |||||||
| chr2:148775878 | C | T | 3 | a0001c0001t0001g0239 a0001c0001t0001g0244 a0001c0001t0001g0245 |
3 | HG01891.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1720+4491C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148775878 | |||||||
| chr2:148775922 | T | C | 1 | a0001c0001t0001g0153 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1720+4535T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148775922 | |||||||
| chr2:148775927 | A | G | 4 | a0001c0001t0002g0072 a0001c0001t0002g0086 a0001c0001t0002g0103 others(1): Show |
4 | HG02074.hp1 HG02523.hp1 NA18747.hp2 others(1): Show |
intron_variant | MODIFIER | c.1720+4540A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148775927 | |||||||
| chr2:148775972 | A | G | 11 | a0001c0001t0001g0136 a0001c0001t0001g0141 a0001c0001t0001g0142 others(8): Show |
11 | HG00544.hp1 HG00558.hp1 HG01981.hp1 others(8): Show |
intron_variant | MODIFIER | c.1720+4585A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148775972 | |||||||
| chr2:148775982 | T | C | 1 | a0001c0001t0001g0178 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1720+4595T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148775982 | |||||||
| chr2:148776014 | C | G | 12 | a0001c0001t0001g0171 a0001c0001t0001g0189 a0001c0001t0001g0190 others(9): Show |
12 | HG00639.hp1 HG02109.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.1720+4627C>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148776014 | |||||||
| chr2:148776016 | C | T | 10 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0178 others(7): Show |
11 | HG00544.hp2 HG00609.hp2 HG01106.hp2 others(8): Show |
intron_variant | MODIFIER | c.1720+4629C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148776016 | |||||||
| chr2:148776137 | G | GAT | 290 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(287): Show |
291 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(288): Show |
intron_variant | MODIFIER | c.1720+4750_1720+475 others(6): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148776137 | |||||||
| chr2:148776195 | A | C | 5 | a0001c0001t0001g0274 a0001c0001t0001g0275 a0001c0001t0001g0276 others(2): Show |
5 | HG02572.hp1 HG02615.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1720+4808A>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148776195 | |||||||
| chr2:148776195 | A | G | 3 | a0001c0001t0001g0036 a0001c0001t0001g0042 a0001c0001t0001g0043 |
3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1720+4808A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148776195 | |||||||
| chr2:148776336 | A | G | 10 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(7): Show |
10 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(7): Show |
intron_variant | MODIFIER | c.1720+4949A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148776336 | |||||||
| chr2:148776531 | T | C | 10 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(7): Show |
10 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(7): Show |
intron_variant | MODIFIER | c.1721-5113T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148776531 | |||||||
| chr2:148776833 | A | G | 6 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0191 others(3): Show |
6 | HG02109.hp2 HG02258.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1721-4811A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148776833 | |||||||
| chr2:148776846 | G | GTCTC | 3 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0132 |
3 | HG00639.hp2 HG03130.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1721-4790_1721-478 others(8): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr2 | 148776846 | ||||||
| chr2:148776856 | C | CTCTCTTT others(14): Show |
1 | a0001c0001t0001g0251 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1721-4787_1721-478 others(25): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr2 | 148776856 | ||||||
| chr2:148776856 | C | CTCTCTTT others(15): Show |
1 | a0001c0001t0001g0252 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1721-4787_1721-478 others(26): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr2 | 148776856 | ||||||
| chr2:148776856 | C | CTCTTTTT others(3): Show |
1 | a0001c0001t0002g0133 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1721-4787_1721-478 others(14): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr2 | 148776856 | ||||||
| chr2:148776856 | C | CTTTTTTT | 7 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(4): Show |
7 | HG02155.hp1 HG02896.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.1721-4772_1721-476 others(11): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr2 | 148776856 | ||||||
| chr2:148776856 | C | CTTTTTTT others(2): Show |
50 | a0001c0001t0001g0036 a0001c0001t0002g0038 a0001c0001t0002g0040 others(47): Show |
50 | HG00558.hp2 HG00642.hp2 HG00673.hp1 others(47): Show |
intron_variant | MODIFIER | c.1721-4774_1721-476 others(13): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr2 | 148776856 | ||||||
| chr2:148776856 | C | CTTTTTTT others(3): Show |
32 | a0001c0001t0001g0043 a0001c0001t0002g0037 a0001c0001t0002g0041 others(29): Show |
32 | HG00280.hp2 HG01069.hp1 HG01070.hp2 others(29): Show |
intron_variant | MODIFIER | c.1721-4775_1721-476 others(14): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr2 | 148776856 | ||||||
| chr2:148776856 | C | CTTTTTTT others(4): Show |
5 | a0001c0001t0002g0049 a0001c0001t0002g0061 a0001c0001t0002g0064 others(2): Show |
5 | HG01346.hp1 HG03942.hp1 HG04184.hp1 others(2): Show |
intron_variant | MODIFIER | c.1721-4776_1721-476 others(15): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr2 | 148776856 | ||||||
| chr2:148776856 | C | CTTTTTTT others(5): Show |
4 | a0001c0001t0002g0045 a0001c0001t0002g0050 a0001c0001t0002g0051 others(1): Show |
4 | HG00738.hp2 HG01123.hp2 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.1721-4777_1721-476 others(16): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr2 | 148776856 | ||||||
| chr2:148776856 | CT | C | 17 | a0001c0001t0001g0005 a0001c0001t0001g0271 a0001c0001t0001g0272 others(14): Show |
17 | HG01884.hp1 HG02109.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.1721-4766delT | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr2 | 148776856 | ||||||
| chr2:148776856 | CTT | C | 9 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(6): Show |
9 | HG01515.hp2 HG02451.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.1721-4767_1721-476 others(6): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr2 | 148776856 | ||||||
| chr2:148776856 | CTTT | C | 146 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0134 others(143): Show |
147 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(144): Show |
intron_variant | MODIFIER | c.1721-4768_1721-476 others(7): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr2 | 148776856 | ||||||
| chr2:148776859 | T | C | 1 | a0001c0001t0001g0005 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1721-4785T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148776859 | |||||||
| chr2:148776860 | T | C | 3 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 |
3 | HG02451.hp2 HG02970.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1721-4784T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148776860 | |||||||
| chr2:148777108 | C | T | 2 | a0001c0001t0001g0251 a0001c0001t0001g0252 |
2 | HG02572.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1721-4536C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148777108 | |||||||
| chr2:148777302 | T | A | 3 | a0001c0001t0001g0036 a0001c0001t0001g0042 a0001c0001t0001g0043 |
3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1721-4342T>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148777302 | |||||||
| chr2:148777368 | A | C | 1 | a0001c0001t0001g0200 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1721-4276A>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148777368 | |||||||
| chr2:148777527 | AT | A | 108 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(105): Show |
108 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(105): Show |
intron_variant | MODIFIER | c.1721-4116delT | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148777527 | |||||||
| chr2:148777529 | C | A | 108 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(105): Show |
108 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(105): Show |
intron_variant | MODIFIER | c.1721-4115C>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148777529 | |||||||
| chr2:148777530 | T | A | 108 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(105): Show |
108 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(105): Show |
intron_variant | MODIFIER | c.1721-4114T>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148777530 | |||||||
| chr2:148777532 | T | A | 108 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(105): Show |
108 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(105): Show |
intron_variant | MODIFIER | c.1721-4112T>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148777532 | |||||||
| chr2:148777533 | G | C | 108 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(105): Show |
108 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(105): Show |
intron_variant | MODIFIER | c.1721-4111G>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148777533 | |||||||
| chr2:148777534 | T | A | 108 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(105): Show |
108 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(105): Show |
intron_variant | MODIFIER | c.1721-4110T>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148777534 | |||||||
| chr2:148777535 | T | A | 108 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(105): Show |
108 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(105): Show |
intron_variant | MODIFIER | c.1721-4109T>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148777535 | |||||||
| chr2:148777586 | G | A | 9 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(6): Show |
9 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.1721-4058G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148777586 | |||||||
| chr2:148777953 | C | T | 107 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(104): Show |
107 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(104): Show |
intron_variant | MODIFIER | c.1721-3691C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148777953 | |||||||
| chr2:148778251 | C | T | 1 | a0001c0001t0001g0195 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1721-3393C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148778251 | |||||||
| chr2:148778381 | A | G | 5 | a0001c0001t0002g0041 a0001c0001t0002g0071 a0001c0001t0002g0076 others(2): Show |
5 | HG02132.hp2 NA18946.hp2 NA18972.hp2 others(2): Show |
intron_variant | MODIFIER | c.1721-3263A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148778381 | |||||||
| chr2:148778535 | G | GC | 13 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(10): Show |
13 | HG02040.hp2 HG02071.hp2 HG02132.hp1 others(10): Show |
intron_variant | MODIFIER | c.1721-3102dupC | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr2 | 148778535 | ||||||
| chr2:148778543 | G | A | 5 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0001c0003t0001g0249 others(2): Show |
5 | HG01884.hp1 HG02109.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1721-3101G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148778543 | |||||||
| chr2:148778683 | G | A | 12 | a0001c0001t0001g0028 a0001c0001t0001g0274 a0001c0001t0001g0275 others(9): Show |
12 | HG02257.hp1 HG02257.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.1721-2961G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148778683 | |||||||
| chr2:148778705 | T | C | 10 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(7): Show |
10 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(7): Show |
intron_variant | MODIFIER | c.1721-2939T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148778705 | |||||||
| chr2:148778784 | T | C | 1 | a0001c0001t0007g0217 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1721-2860T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148778784 | |||||||
| chr2:148778869 | G | A | 1 | a0001c0001t0002g0090 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1721-2775G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148778869 | |||||||
| chr2:148779141 | C | CA | 95 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(92): Show |
95 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.1721-2497dupA | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr2 | 148779141 | ||||||
| chr2:148779208 | G | C | 107 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(104): Show |
107 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(104): Show |
intron_variant | MODIFIER | c.1721-2436G>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148779208 | |||||||
| chr2:148779210 | A | G | 1 | a0002c0002t0001g0253 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1721-2434A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148779210 | |||||||
| chr2:148779356 | A | C | 3 | a0001c0001t0001g0250 a0001c0001t0001g0251 a0001c0001t0001g0252 |
3 | HG02572.hp2 HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1721-2288A>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148779356 | |||||||
| chr2:148779821 | C | T | 1 | a0001c0001t0002g0113 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1721-1823C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148779821 | |||||||
| chr2:148779863 | C | T | 1 | a0001c0001t0002g0110 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1721-1781C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148779863 | |||||||
| chr2:148779872 | T | C | 1 | a0002c0002t0001g0253 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1721-1772T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148779872 | |||||||
| chr2:148779895 | G | A | 289 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(286): Show |
290 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(287): Show |
intron_variant | MODIFIER | c.1721-1749G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148779895 | |||||||
| chr2:148779951 | T | A | 20 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0001g0184 others(17): Show |
20 | HG00673.hp2 HG02074.hp2 HG04204.hp1 others(17): Show |
intron_variant | MODIFIER | c.1721-1693T>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148779951 | |||||||
| chr2:148780415 | T | A | 82 | a0001c0001t0002g0037 a0001c0001t0002g0038 a0001c0001t0002g0041 others(79): Show |
82 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(79): Show |
intron_variant | MODIFIER | c.1721-1229T>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148780415 | |||||||
| chr2:148780589 | C | T | 1 | a0001c0001t0001g0273 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1721-1055C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148780589 | |||||||
| chr2:148780601 | C | T | 2 | a0001c0001t0001g0198 a0001c0001t0001g0199 |
2 | HG02818.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1721-1043C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148780601 | |||||||
| chr2:148780648 | C | A | 1 | a0001c0001t0001g0170 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1721-996C>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148780648 | |||||||
| chr2:148780849 | A | G | 3 | a0001c0001t0001g0148 a0001c0001t0001g0150 a0001c0001t0001g0154 |
3 | NA19005.hp2 NA19064.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.1721-795A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148780849 | |||||||
| chr2:148781280 | T | A | 3 | a0001c0001t0001g0036 a0001c0001t0001g0042 a0001c0001t0001g0043 |
3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1721-364T>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148781280 | |||||||
| chr2:148781485 | G | A | 114 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(111): Show |
114 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(111): Show |
intron_variant | MODIFIER | c.1721-159G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148781485 | |||||||
| chr2:148781491 | T | G | 111 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0134 others(108): Show |
111 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(108): Show |
intron_variant | MODIFIER | c.1721-153T>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148781491 | |||||||
| chr2:148781562 | A | G | 1 | a0001c0001t0001g0304 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1721-82A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 10/13 | chr2 | 148781562 | |||||||
| chr2:148781862 | G | C | 6 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0191 others(3): Show |
6 | HG02109.hp2 HG02258.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1857+82G>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 11/13 | chr2 | 148781862 | |||||||
| chr2:148782018 | G | C | 1 | a0001c0001t0001g0028 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1857+238G>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 11/13 | chr2 | 148782018 | |||||||
| chr2:148782147 | T | C | 1 | a0001c0001t0002g0069 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1857+367T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 11/13 | chr2 | 148782147 | |||||||
| chr2:148782256 | A | G | 1 | a0001c0001t0001g0025 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1857+476A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 11/13 | chr2 | 148782256 | |||||||
| chr2:148782351 | A | G | 1 | a0001c0001t0002g0044 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1857+571A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 11/13 | chr2 | 148782351 | |||||||
| chr2:148782398 | A | T | 1 | a0001c0001t0001g0260 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1857+618A>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 11/13 | chr2 | 148782398 | |||||||
| chr2:148782486 | A | AT | 3 | a0001c0001t0001g0036 a0001c0001t0001g0042 a0001c0001t0001g0043 |
3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1857+706_1857+707i others(3): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 11/13 | chr2 | 148782486 | |||||||
| chr2:148782488 | G | GGACT | 3 | a0001c0001t0001g0036 a0001c0001t0001g0042 a0001c0001t0001g0043 |
3 | HG02145.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1857+708_1857+709i others(6): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 11/13 | chr2 | 148782488 | |||||||
| chr2:148782543 | AAAC | A | 86 | a0001c0001t0002g0037 a0001c0001t0002g0038 a0001c0001t0002g0040 others(83): Show |
86 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(83): Show |
intron_variant | MODIFIER | c.1857+766_1857+768d others(5): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr2 | 148782543 | ||||||
| chr2:148782544 | AAC | A | 20 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(17): Show |
20 | HG00639.hp2 HG02040.hp2 HG02080.hp2 others(17): Show |
intron_variant | MODIFIER | c.1857+766_1857+767d others(4): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr2 | 148782544 | ||||||
| chr2:148782602 | G | A | 1 | a0001c0001t0001g0136 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1857+822G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 11/13 | chr2 | 148782602 | |||||||
| chr2:148782671 | G | A | 1 | a0001c0001t0001g0141 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1857+891G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 11/13 | chr2 | 148782671 | |||||||
| chr2:148782692 | C | T | 4 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(1): Show |
4 | HG00639.hp2 HG02809.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1858-905C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 11/13 | chr2 | 148782692 | |||||||
| chr2:148782715 | A | G | 1 | a0001c0001t0001g0265 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1858-882A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 11/13 | chr2 | 148782715 | |||||||
| chr2:148782761 | T | TTTCTC | 289 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(286): Show |
290 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(287): Show |
intron_variant | MODIFIER | c.1858-834_1858-833i others(7): Show |
EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr2 | 148782761 | ||||||
| chr2:148783067 | G | T | 11 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0178 others(8): Show |
12 | HG00544.hp2 HG00609.hp2 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.1858-530G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 11/13 | chr2 | 148783067 | |||||||
| chr2:148783407 | T | C | 1 | a0001c0001t0001g0280 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1858-190T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 11/13 | chr2 | 148783407 | |||||||
| chr2:148783541 | T | C | 1 | a0001c0001t0001g0231 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1858-56T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 11/13 | chr2 | 148783541 | |||||||
| chr2:148783910 | A | G | 3 | a0001c0001t0002g0066 a0001c0001t0002g0111 a0001c0001t0002g0123 |
3 | HG00280.hp2 HG00741.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.2017+154A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 12/13 | chr2 | 148783910 | |||||||
| chr2:148783975 | G | C | 1 | a0001c0001t0002g0127 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2017+219G>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 12/13 | chr2 | 148783975 | |||||||
| chr2:148784250 | T | C | 1 | a0001c0001t0001g0261 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2018-418T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 12/13 | chr2 | 148784250 | |||||||
| chr2:148784357 | A | C | 72 | a0001c0001t0002g0037 a0001c0001t0002g0040 a0001c0001t0002g0041 others(69): Show |
72 | HG00423.hp2 HG00558.hp2 HG00673.hp1 others(69): Show |
intron_variant | MODIFIER | c.2018-311A>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 12/13 | chr2 | 148784357 | |||||||
| chr2:148784410 | A | G | 1 | a0001c0001t0002g0128 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.2018-258A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 12/13 | chr2 | 148784410 | |||||||
| chr2:148784490 | G | A | 9 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(6): Show |
9 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.2018-178G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 12/13 | chr2 | 148784490 | |||||||
| chr2:148785112 | A | G | 1 | a0001c0001t0001g0182 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.2351+111A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 13/13 | chr2 | 148785112 | |||||||
| chr2:148785298 | A | G | 10 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(7): Show |
10 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(7): Show |
intron_variant | MODIFIER | c.2351+297A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 13/13 | chr2 | 148785298 | |||||||
| chr2:148785314 | T | A | 2 | a0001c0001t0001g0208 a0001c0001t0001g0219 |
2 | HG00738.hp1 HG01070.hp1 |
intron_variant | MODIFIER | c.2351+313T>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 13/13 | chr2 | 148785314 | |||||||
| chr2:148785322 | C | T | 1 | a0001c0001t0001g0028 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2351+321C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 13/13 | chr2 | 148785322 | |||||||
| chr2:148785389 | G | A | 1 | a0001c0001t0002g0059 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.2351+388G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 13/13 | chr2 | 148785389 | |||||||
| chr2:148785458 | G | T | 1 | a0001c0001t0001g0267 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2351+457G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 13/13 | chr2 | 148785458 | |||||||
| chr2:148785463 | G | T | 1 | a0001c0001t0001g0267 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2351+462G>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 13/13 | chr2 | 148785463 | |||||||
| chr2:148785472 | C | T | 1 | a0001c0001t0001g0279 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2351+471C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 13/13 | chr2 | 148785472 | |||||||
| chr2:148785669 | A | G | 5 | a0001c0001t0004g0001 a0001c0001t0004g0173 a0001c0001t0004g0176 others(2): Show |
6 | HG00544.hp2 HG00609.hp2 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.2352-636A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 13/13 | chr2 | 148785669 | |||||||
| chr2:148785774 | C | T | 1 | a0001c0001t0001g0003 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2352-531C>T | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 13/13 | chr2 | 148785774 | |||||||
| chr2:148785892 | G | A | 7 | a0001c0001t0001g0036 a0001c0001t0001g0042 a0001c0001t0001g0043 others(4): Show |
7 | HG00639.hp2 HG02145.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.2352-413G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 13/13 | chr2 | 148785892 | |||||||
| chr2:148785977 | T | C | 7 | a0001c0001t0001g0036 a0001c0001t0001g0042 a0001c0001t0001g0043 others(4): Show |
7 | HG00639.hp2 HG02145.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.2352-328T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 13/13 | chr2 | 148785977 | |||||||
| chr2:148785986 | A | G | 1 | a0001c0001t0001g0258 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2352-319A>G | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 13/13 | chr2 | 148785986 | |||||||
| chr2:148786136 | G | A | 9 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(6): Show |
9 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.2352-169G>A | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 13/13 | chr2 | 148786136 | |||||||
| chr2:148786149 | T | C | 10 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0030 others(7): Show |
10 | HG02040.hp2 HG02132.hp1 HG02155.hp1 others(7): Show |
intron_variant | MODIFIER | c.2352-156T>C | EPC2 | ENSG00000135999.12 | transcript | ENST00000258484.11 | protein_coding | 13/13 | chr2 | 148786149 |