Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 9694 |
| ensemblid | ENSG00000104412.8 |
| hgncid | 28963 |
| symbol | EMC2 |
| name | ER membrane protein complex subunit 2 |
| refseq_nuc | NM_014673.5 |
| refseq_prot | NP_055488.1 |
| ensembl_nuc | ENST00000220853.8 |
| ensembl_prot | ENSP00000220853.3 |
| mane_status | MANE Select |
| chr | chr8 |
| start | 108443624 |
| end | 108489196 |
| strand | + |
| ver | v1.2 |
| region | chr8:108443624-108489196 |
| region5000 | chr8:108438624-108494196 |
| regionname0 | EMC2_chr8_108443624_108489196 |
| regionname5000 | EMC2_chr8_108438624_108494196 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 297 | 362 | 89 | 64 | 143 | 18 | 46 | 109 | EMC2_chr8_108438624_108494196 | EMC2 | MAKVS others(292): Show |
chr8 | 108438624 | 108494196 |
| a0002 | 0/0 | 297 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | MAKVS others(292): Show |
chr8 | 108438624 | 108494196 |
| a0003 | 0/0 | 297 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | EMC2_chr8_108438624_108494196 | EMC2 | MAKVS others(292): Show |
chr8 | 108438624 | 108494196 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 891 | 359 | 86 | 64 | 143 | 18 | 46 | EMC2_chr8_108438624_108494196 | EMC2 | ATGGC others(886): Show |
chr8 | 108438624 | 108494196 | ||
| a0001c0002 | 0/0 | 891 | 3 | 3 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | ATGGC others(886): Show |
chr8 | 108438624 | 108494196 | ||
| a0002c0003 | 0/0 | 891 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | ATGGC others(886): Show |
chr8 | 108438624 | 108494196 | ||
| a0003c0004 | 0/0 | 891 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | ATGGC others(886): Show |
chr8 | 108438624 | 108494196 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 3527 | 123 | 16 | 28 | 64 | 6 | 8 | EMC2_chr8_108438624_108494196 | EMC2 | GCCCT others(3522): Show |
chr8 | 108438624 | 108494196 |
| a0001c0001t0002 | 0/1 | 3526 | 88 | 0 | 10 | 55 | 6 | 16 | EMC2_chr8_108438624_108494196 | EMC2 | GCCCT others(3521): Show |
chr8 | 108438624 | 108494196 |
| a0001c0001t0003 | 0/0 | 3526 | 52 | 11 | 10 | 17 | 5 | 9 | EMC2_chr8_108438624_108494196 | EMC2 | GCCCT others(3521): Show |
chr8 | 108438624 | 108494196 |
| a0001c0001t0004 | 0/0 | 3526 | 27 | 21 | 3 | 0 | 0 | 3 | EMC2_chr8_108438624_108494196 | EMC2 | GCCCT others(3521): Show |
chr8 | 108438624 | 108494196 |
| a0001c0001t0005 | 0/0 | 3527 | 10 | 9 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | GCCCT others(3522): Show |
chr8 | 108438624 | 108494196 |
| a0001c0001t0006 | 0/0 | 3526 | 10 | 1 | 4 | 1 | 0 | 4 | EMC2_chr8_108438624_108494196 | EMC2 | GCCCT others(3521): Show |
chr8 | 108438624 | 108494196 |
| a0001c0001t0007 | 0/0 | 3526 | 5 | 5 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | GCCCT others(3521): Show |
chr8 | 108438624 | 108494196 |
| a0001c0001t0008 | 0/0 | 3527 | 4 | 4 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | GCCCT others(3522): Show |
chr8 | 108438624 | 108494196 |
| a0001c0001t0009 | 0/0 | 3526 | 4 | 4 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | GCCCT others(3521): Show |
chr8 | 108438624 | 108494196 |
| a0001c0001t0010 | 0/0 | 3527 | 4 | 0 | 3 | 0 | 0 | 1 | EMC2_chr8_108438624_108494196 | EMC2 | GCCCT others(3522): Show |
chr8 | 108438624 | 108494196 |
| a0001c0001t0011 | 0/0 | 3527 | 3 | 3 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | GCCCT others(3522): Show |
chr8 | 108438624 | 108494196 |
| a0001c0001t0012 | 0/0 | 3526 | 3 | 0 | 0 | 0 | 0 | 3 | EMC2_chr8_108438624_108494196 | EMC2 | GCCCT others(3521): Show |
chr8 | 108438624 | 108494196 |
| a0001c0001t0013 | 0/0 | 3526 | 3 | 0 | 0 | 3 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | GCCCT others(3521): Show |
chr8 | 108438624 | 108494196 |
| a0001c0001t0014 | 0/0 | 3526 | 2 | 1 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | GCCCT others(3521): Show |
chr8 | 108438624 | 108494196 |
| a0001c0001t0015 | 0/0 | 3526 | 2 | 2 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | GCCCT others(3521): Show |
chr8 | 108438624 | 108494196 |
| a0001c0001t0016 | 0/0 | 3527 | 2 | 2 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | GCCCT others(3522): Show |
chr8 | 108438624 | 108494196 |
| a0001c0001t0017 | 0/0 | 3526 | 2 | 2 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | GCCCT others(3521): Show |
chr8 | 108438624 | 108494196 |
| a0001c0001t0018 | 0/0 | 3526 | 1 | 0 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | GCCCT others(3521): Show |
chr8 | 108438624 | 108494196 |
| a0001c0001t0019 | 0/0 | 3527 | 2 | 0 | 0 | 0 | 1 | 1 | EMC2_chr8_108438624_108494196 | EMC2 | GCCCT others(3522): Show |
chr8 | 108438624 | 108494196 |
| a0001c0001t0020 | 0/0 | 3526 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | GCCCT others(3521): Show |
chr8 | 108438624 | 108494196 |
| a0001c0001t0021 | 0/0 | 3526 | 1 | 0 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | GCCCT others(3521): Show |
chr8 | 108438624 | 108494196 |
| a0001c0001t0022 | 0/0 | 3526 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | GCCCT others(3521): Show |
chr8 | 108438624 | 108494196 |
| a0001c0001t0023 | 0/0 | 3527 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | GCCCT others(3522): Show |
chr8 | 108438624 | 108494196 |
| a0001c0001t0024 | 0/0 | 3526 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | GCCCT others(3521): Show |
chr8 | 108438624 | 108494196 |
| a0001c0001t0025 | 0/0 | 3527 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | GCCCT others(3522): Show |
chr8 | 108438624 | 108494196 |
| a0001c0001t0026 | 0/0 | 3526 | 1 | 0 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | GCCCT others(3521): Show |
chr8 | 108438624 | 108494196 |
| a0001c0001t0027 | 0/0 | 3527 | 1 | 0 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | GCCCT others(3522): Show |
chr8 | 108438624 | 108494196 |
| a0001c0001t0028 | 0/0 | 3526 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | GCCCT others(3521): Show |
chr8 | 108438624 | 108494196 |
| a0001c0001t0029 | 0/0 | 3526 | 1 | 0 | 0 | 0 | 0 | 1 | EMC2_chr8_108438624_108494196 | EMC2 | GCCCT others(3521): Show |
chr8 | 108438624 | 108494196 |
| a0001c0001t0030 | 0/0 | 3527 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | GCCCT others(3522): Show |
chr8 | 108438624 | 108494196 |
| a0001c0001t0031 | 0/0 | 3526 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | GCCCT others(3521): Show |
chr8 | 108438624 | 108494196 |
| a0001c0002t0003 | 0/0 | 3526 | 3 | 3 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | GCCCT others(3521): Show |
chr8 | 108438624 | 108494196 |
| a0002c0003t0018 | 0/0 | 3526 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | GCCCT others(3521): Show |
chr8 | 108438624 | 108494196 |
| a0003c0004t0002 | 0/0 | 3526 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | GCCCT others(3521): Show |
chr8 | 108438624 | 108494196 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 25 | 4 | 4 | 16 | 0 | 1 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0001g0009 | 0/0 | 4 | 1 | 0 | 3 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0001g0010 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0001g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0001g0044 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0001g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0001g0047 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0001g0048 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0001g0049 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0001g0208 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0002g0003 | 0/0 | 8 | 0 | 0 | 6 | 0 | 2 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0002g0004 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0002g0005 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0002g0007 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0002g0008 | 0/0 | 4 | 0 | 2 | 0 | 1 | 1 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0002g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0002g0022 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0002g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0002g0024 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0002g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0002g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0002g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0002g0137 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0003g0002 | 0/0 | 12 | 0 | 1 | 11 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0003g0006 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0003g0012 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0003g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0003g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0003g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0003g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0003g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0003g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0003g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0003g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0003g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0003g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0003g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0003g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0003g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0003g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0003g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0003g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0003g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0003g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0003g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0003g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0003g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0003g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0003g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0003g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0003g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0003g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0003g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0003g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0003g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0004g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0004g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0004g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0004g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0004g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0004g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0004g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0004g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0004g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0004g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0004g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0004g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0004g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0004g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0004g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0004g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0004g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0004g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0004g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0004g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0004g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0004g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0004g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0005g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0005g0050 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0005g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0005g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0005g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0005g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0005g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0005g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0006g0016 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0006g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0006g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0006g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0006g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0006g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0006g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0007g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0007g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0007g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0008g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0008g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0008g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0008g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0009g0011 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0009g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0010g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0010g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0010g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0010g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0011g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0012g0019 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0012g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0013g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0014g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0014g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0015g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0016g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0016g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0017g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0017g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0018g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0019g0033 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0020g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0021g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0022g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0023g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0024g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0025g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0026g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0027g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0028g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0029g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0030g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0001t0031g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0002t0003g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0002t0003g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0001c0002t0003g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0002c0003t0018g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| a0003c0004t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0003 | g0096 | EUR | GBR | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0040 | EUR | GBR | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0037 | EUR | GBR | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG00140 | hp2 | a0001 | c0001 | t0003 | g0072 | EUR | GBR | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG00280 | hp1 | a0001 | c0001 | t0003 | g0093 | EUR | FIN | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0198 | EUR | FIN | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0185 | EUR | FIN | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG00323 | hp2 | a0001 | c0001 | t0003 | g0066 | EUR | FIN | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG00423 | hp2 | a0001 | c0001 | t0003 | g0098 | EAS | CHS | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | CHS | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | CHS | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0123 | EAS | CHS | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | CHS | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | CHS | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | CHS | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | CHS | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG00609 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | CHS | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | CHS | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0141 | EAS | CHS | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | PUR | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0199 | AMR | PUR | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | PUR | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG00733 | hp1 | a0001 | c0001 | t0003 | g0068 | AMR | PUR | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG00733 | hp2 | a0001 | c0001 | t0004 | g0059 | AMR | PUR | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG00735 | hp2 | a0001 | c0001 | t0010 | g0200 | AMR | PUR | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG00738 | hp1 | a0001 | c0001 | t0006 | g0032 | AMR | PUR | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0131 | AMR | PUR | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0207 | AMR | PUR | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG00741 | hp2 | a0001 | c0001 | t0003 | g0095 | AMR | PUR | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG01069 | hp1 | a0001 | c0001 | t0003 | g0094 | AMR | PUR | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0027 | AMR | PUR | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG01070 | hp1 | a0001 | c0001 | t0003 | g0077 | AMR | PUR | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG01070 | hp2 | a0001 | c0001 | t0021 | g0190 | AMR | PUR | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0027 | AMR | PUR | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG01071 | hp2 | a0001 | c0001 | t0003 | g0002 | AMR | PUR | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0209 | AMR | PUR | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG01074 | hp2 | a0001 | c0001 | t0006 | g0032 | AMR | PUR | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0008 | AMR | PUR | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | PUR | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG01099 | hp1 | a0001 | c0001 | t0026 | g0082 | AMR | PUR | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG01099 | hp2 | a0001 | c0001 | t0010 | g0215 | AMR | PUR | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0243 | AMR | PUR | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG01106 | hp2 | a0001 | c0001 | t0003 | g0012 | AMR | PUR | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG01109 | hp2 | a0001 | c0001 | t0018 | g0062 | AMR | PUR | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0239 | AMR | PUR | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG01167 | hp2 | a0001 | c0001 | t0014 | g0169 | AMR | PUR | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG01168 | hp1 | a0001 | c0001 | t0003 | g0012 | AMR | PUR | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG01168 | hp2 | a0001 | c0001 | t0003 | g0028 | AMR | PUR | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0242 | AMR | PUR | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG01169 | hp2 | a0001 | c0001 | t0003 | g0028 | AMR | PUR | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0108 | AMR | PUR | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG01243 | hp1 | a0001 | c0001 | t0004 | g0159 | AMR | PUR | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG01243 | hp2 | a0001 | c0001 | t0005 | g0172 | AMR | PUR | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG01255 | hp2 | a0001 | c0001 | t0006 | g0016 | AMR | CLM | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0240 | AMR | CLM | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0205 | AMR | CLM | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | CLM | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | CLM | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | CLM | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0206 | AMR | CLM | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG01261 | hp1 | a0001 | c0001 | t0004 | g0225 | AMR | CLM | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG01261 | hp2 | a0001 | c0001 | t0027 | g0216 | AMR | CLM | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0241 | AMR | CLM | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG01361 | hp2 | a0001 | c0001 | t0010 | g0214 | AMR | CLM | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0196 | AMR | CLM | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0134 | AMR | CLM | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0135 | EUR | IBS | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0107 | EUR | IBS | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0245 | EUR | IBS | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0037 | EUR | IBS | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0008 | EUR | IBS | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0244 | EUR | IBS | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG01884 | hp1 | a0001 | c0001 | t0004 | g0015 | AFR | ACB | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG01884 | hp2 | a0001 | c0001 | t0011 | g0014 | AFR | ACB | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG01891 | hp1 | a0001 | c0001 | t0004 | g0015 | AFR | ACB | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG01891 | hp2 | a0001 | c0001 | t0003 | g0006 | AFR | ACB | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | PEL | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | PEL | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG01952 | hp1 | a0001 | c0001 | t0003 | g0074 | AMR | PEL | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0238 | AMR | PEL | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0132 | AMR | PEL | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG02004 | hp1 | a0001 | c0001 | t0006 | g0165 | AMR | PEL | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0237 | AMR | PEL | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG02015 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | KHV | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | KHV | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG02027 | hp1 | a0001 | c0001 | t0006 | g0168 | EAS | KHV | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG02027 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | KHV | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | KHV | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | KHV | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG02055 | hp1 | a0001 | c0001 | t0003 | g0088 | AFR | ACB | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG02055 | hp2 | a0001 | c0001 | t0005 | g0151 | AFR | ACB | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0105 | EAS | KHV | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | KHV | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0120 | EAS | KHV | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG02074 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | KHV | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | KHV | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0109 | EAS | KHV | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | KHV | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG02132 | hp2 | a0001 | c0001 | t0003 | g0078 | EAS | KHV | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0235 | AFR | ACB | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG02145 | hp2 | a0001 | c0001 | t0004 | g0031 | AFR | ACB | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | CDX | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0106 | EAS | CDX | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG02165 | hp1 | a0001 | c0001 | t0003 | g0075 | EAS | CDX | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG02257 | hp1 | a0001 | c0001 | t0003 | g0065 | AFR | ACB | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG02257 | hp2 | a0001 | c0001 | t0007 | g0100 | AFR | ACB | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG02258 | hp1 | a0001 | c0001 | t0004 | g0160 | AFR | ACB | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG02280 | hp2 | a0001 | c0001 | t0003 | g0006 | AFR | ACB | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | PEL | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0211 | AMR | PEL | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG02451 | hp1 | a0001 | c0001 | t0005 | g0050 | AFR | ACB | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG02451 | hp2 | a0001 | c0001 | t0014 | g0170 | AFR | ACB | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | KHV | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG02572 | hp1 | a0001 | c0001 | t0004 | g0158 | AFR | GWD | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0233 | AFR | GWD | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG02615 | hp1 | a0001 | c0001 | t0004 | g0145 | AFR | GWD | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG02615 | hp2 | a0001 | c0001 | t0004 | g0164 | AFR | GWD | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | GWD | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG02630 | hp1 | a0001 | c0001 | t0024 | g0067 | AFR | GWD | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG02630 | hp2 | a0001 | c0001 | t0022 | g0052 | AFR | GWD | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG02647 | hp2 | a0001 | c0001 | t0005 | g0050 | AFR | GWD | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0022 | SAS | PJL | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG02683 | hp2 | a0001 | c0001 | t0004 | g0058 | SAS | PJL | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0133 | SAS | PJL | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG02698 | hp2 | a0001 | c0001 | t0003 | g0079 | SAS | PJL | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG02717 | hp1 | a0001 | c0001 | t0004 | g0147 | AFR | GWD | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG02717 | hp2 | a0001 | c0001 | t0008 | g0220 | AFR | GWD | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0112 | SAS | PJL | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG02735 | hp2 | a0001 | c0001 | t0006 | g0016 | SAS | PJL | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0036 | SAS | PJL | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG02809 | hp1 | a0001 | c0001 | t0005 | g0034 | AFR | GWD | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG02809 | hp2 | a0001 | c0001 | t0003 | g0006 | AFR | GWD | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG02886 | hp1 | a0001 | c0001 | t0016 | g0055 | AFR | GWD | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG02886 | hp2 | a0001 | c0001 | t0004 | g0029 | AFR | GWD | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | GWD | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG02895 | hp2 | a0001 | c0001 | t0017 | g0029 | AFR | GWD | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG02896 | hp1 | a0001 | c0001 | t0015 | g0045 | AFR | GWD | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG02896 | hp2 | a0001 | c0001 | t0007 | g0021 | AFR | GWD | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG02897 | hp1 | a0001 | c0001 | t0007 | g0021 | AFR | GWD | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG02897 | hp2 | a0001 | c0001 | t0017 | g0146 | AFR | GWD | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG02922 | hp1 | a0001 | c0001 | t0008 | g0218 | AFR | ESN | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG02922 | hp2 | a0001 | c0001 | t0004 | g0030 | AFR | ESN | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG02965 | hp1 | a0001 | c0001 | t0008 | g0219 | AFR | ESN | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG02965 | hp2 | a0001 | c0001 | t0009 | g0011 | AFR | ESN | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG02970 | hp1 | a0001 | c0001 | t0025 | g0203 | AFR | ESN | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG02970 | hp2 | a0001 | c0002 | t0003 | g0092 | AFR | ESN | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG02976 | hp1 | a0002 | c0003 | t0018 | g0063 | AFR | ESN | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG02976 | hp2 | a0001 | c0001 | t0004 | g0163 | AFR | ESN | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0188 | SAS | PJL | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0053 | SAS | PJL | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | GWD | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG03041 | hp2 | a0001 | c0002 | t0003 | g0089 | AFR | GWD | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG03098 | hp1 | a0001 | c0001 | t0011 | g0014 | AFR | MSL | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG03098 | hp2 | a0001 | c0001 | t0004 | g0148 | AFR | MSL | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG03130 | hp1 | a0001 | c0001 | t0003 | g0090 | AFR | ESN | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG03130 | hp2 | a0001 | c0001 | t0007 | g0020 | AFR | ESN | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG03139 | hp1 | a0001 | c0001 | t0004 | g0030 | AFR | ESN | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG03139 | hp2 | a0001 | c0001 | t0004 | g0171 | AFR | ESN | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG03209 | hp1 | a0001 | c0001 | t0003 | g0064 | AFR | MSL | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | MSL | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG03225 | hp1 | a0001 | c0001 | t0006 | g0149 | AFR | MSL | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG03225 | hp2 | a0001 | c0001 | t0005 | g0246 | AFR | MSL | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG03239 | hp1 | a0001 | c0001 | t0004 | g0054 | SAS | PJL | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG03239 | hp2 | a0001 | c0001 | t0029 | g0003 | SAS | PJL | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG03453 | hp1 | a0001 | c0001 | t0005 | g0034 | AFR | MSL | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG03453 | hp2 | a0001 | c0001 | t0015 | g0045 | AFR | MSL | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | MSL | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | MSL | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0035 | SAS | PJL | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG03490 | hp2 | a0001 | c0001 | t0003 | g0076 | SAS | PJL | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG03491 | hp1 | a0001 | c0001 | t0003 | g0071 | SAS | PJL | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG03491 | hp2 | a0001 | c0001 | t0012 | g0019 | SAS | PJL | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG03492 | hp1 | a0001 | c0001 | t0012 | g0019 | SAS | PJL | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0036 | SAS | PJL | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG03516 | hp1 | a0001 | c0001 | t0004 | g0015 | AFR | ESN | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG03516 | hp2 | a0001 | c0001 | t0007 | g0020 | AFR | ESN | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG03540 | hp1 | a0001 | c0001 | t0020 | g0154 | AFR | GWD | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG03540 | hp2 | a0001 | c0001 | t0009 | g0011 | AFR | GWD | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG03579 | hp1 | a0001 | c0001 | t0004 | g0167 | AFR | MSL | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG03579 | hp2 | a0001 | c0001 | t0008 | g0217 | AFR | MSL | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0143 | SAS | PJL | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG03654 | hp2 | a0001 | c0001 | t0006 | g0166 | SAS | PJL | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG03669 | hp2 | a0001 | c0001 | t0003 | g0083 | SAS | PJL | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG03688 | hp1 | a0001 | c0001 | t0019 | g0033 | SAS | STU | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0008 | SAS | STU | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0022 | SAS | PJL | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0127 | SAS | PJL | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG03710 | hp1 | a0001 | c0001 | t0003 | g0099 | SAS | PJL | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG03710 | hp2 | a0001 | c0001 | t0010 | g0201 | SAS | PJL | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0228 | SAS | BEB | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG03831 | hp2 | a0001 | c0001 | t0012 | g0061 | SAS | BEB | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0024 | SAS | BEB | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0180 | SAS | BEB | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0119 | SAS | BEB | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG03942 | hp1 | a0001 | c0001 | t0006 | g0161 | SAS | BEB | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG03942 | hp2 | a0001 | c0001 | t0003 | g0081 | SAS | BEB | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG04115 | hp1 | a0001 | c0001 | t0006 | g0016 | SAS | STU | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG04115 | hp2 | a0001 | c0001 | t0003 | g0084 | SAS | STU | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0116 | SAS | BEB | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0187 | SAS | BEB | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0110 | SAS | STU | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG04204 | hp2 | a0001 | c0001 | t0003 | g0073 | SAS | STU | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0130 | SAS | STU | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG04228 | hp2 | a0001 | c0001 | t0003 | g0085 | SAS | STU | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| NA18522 | hp1 | a0001 | c0001 | t0005 | g0152 | AFR | YRI | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| NA18522 | hp2 | a0001 | c0001 | t0004 | g0155 | AFR | YRI | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0230 | EAS | CHB | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| NA18906 | hp1 | a0001 | c0001 | t0009 | g0060 | AFR | YRI | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| NA18906 | hp2 | a0001 | c0001 | t0005 | g0150 | AFR | YRI | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0142 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| NA18947 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| NA18948 | hp2 | a0001 | c0001 | t0013 | g0003 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| NA18950 | hp1 | a0001 | c0001 | t0003 | g0080 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| NA18952 | hp1 | a0001 | c0001 | t0003 | g0086 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| NA18956 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| NA18957 | hp2 | a0001 | c0001 | t0013 | g0003 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0140 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| NA18963 | hp1 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| NA18964 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| NA18975 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| NA18976 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| NA18976 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0231 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| NA18979 | hp1 | a0001 | c0001 | t0013 | g0003 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| NA18979 | hp2 | a0001 | c0001 | t0023 | g0213 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0138 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0124 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| NA18985 | hp1 | a0003 | c0004 | t0002 | g0128 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0101 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| NA19001 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| NA19006 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| NA19007 | hp1 | a0001 | c0001 | t0031 | g0117 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| NA19010 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| NA19012 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| NA19030 | hp1 | a0001 | c0001 | t0004 | g0156 | AFR | LWK | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| NA19030 | hp2 | a0001 | c0001 | t0005 | g0153 | AFR | LWK | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | LWK | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| NA19043 | hp2 | a0001 | c0001 | t0009 | g0011 | AFR | LWK | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0114 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| NA19062 | hp1 | a0001 | c0001 | t0030 | g0232 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0139 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0122 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| NA19070 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| NA19072 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0118 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0113 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0121 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| NA19084 | hp2 | a0001 | c0001 | t0003 | g0097 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| NA19240 | hp1 | a0001 | c0001 | t0003 | g0069 | AFR | YRI | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| NA19240 | hp2 | a0001 | c0001 | t0004 | g0157 | AFR | YRI | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| NA20129 | hp1 | a0001 | c0002 | t0003 | g0091 | AFR | ASW | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| NA20129 | hp2 | a0001 | c0001 | t0004 | g0162 | AFR | ASW | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0049 | EUR | TSI | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| NA20752 | hp2 | a0001 | c0001 | t0019 | g0033 | EUR | TSI | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0024 | EUR | TSI | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| NA20805 | hp2 | a0001 | c0001 | t0003 | g0012 | EUR | TSI | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| NA20905 | hp1 | a0001 | c0001 | t0004 | g0057 | SAS | GIH | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0111 | SAS | GIH | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | CLM | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0008 | AMR | CLM | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0234 | AFR | ACB | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG02109 | hp2 | a0001 | c0001 | t0003 | g0070 | AFR | ACB | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG02486 | hp1 | a0001 | c0001 | t0011 | g0014 | AFR | ACB | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG02486 | hp2 | a0001 | c0001 | t0016 | g0056 | AFR | ACB | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG02559 | hp1 | a0001 | c0001 | t0003 | g0087 | AFR | ACB | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG02559 | hp2 | a0001 | c0001 | t0004 | g0031 | AFR | ACB | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG03471 | hp1 | a0001 | c0001 | t0003 | g0006 | AFR | MSL | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | MSL | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| NA20300 | hp1 | a0001 | c0001 | t0028 | g0236 | AFR | USA | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | USA | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0137 | REF | REF | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0208 | REF | REF | EMC2_chr8_108438624_108494196 | EMC2 | chr8 | 108438624 | 108494196 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:108469887 | G | A | 1 | a0002 | 1 | HG02976.hp1 | missense_variant | MODERATE | c.425G>A | p.Arg142Gln | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 6/11 | 460/3527 | 425/894 | 142/297 | chr8 | 108469887 | |||
| chr8:108476797 | G | A | 1 | a0003 | 1 | NA18985.hp1 | missense_variant | MODERATE | c.607G>A | p.Gly203Ser | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 9/11 | 642/3527 | 607/894 | 203/297 | chr8 | 108476797 | |||
| chr8:108476885 | T | A | 1 | a0003 | 1 | NA18985.hp1 | missense_variant | MODERATE | c.695T>A | p.Leu232His | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 9/11 | 730/3527 | 695/894 | 232/297 | chr8 | 108476885 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:108479008 | G | A | 1 | a0001c0002 | 3 | HG02970.hp2 HG03041.hp2 NA20129.hp1 |
splice_region_variant&synonymous_variant | LOW | c.705G>A | p.Ser235Ser | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/11 | 740/3527 | 705/894 | 235/297 | chr8 | 108479008 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:108443634 | C | T | 8 | a0001c0001t0002 a0001c0001t0013 a0001c0001t0027 others(5): Show |
96 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(93): Show |
5_prime_UTR_variant | MODIFIER | c.-25C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/11 | 25 | chr8 | 108443634 | ||||||
| chr8:108443642 | C | G | 1 | a0001c0001t0026 | 1 | HG01099.hp1 | 5_prime_UTR_variant | MODIFIER | c.-17C>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/11 | 17 | chr8 | 108443642 | ||||||
| chr8:108486619 | A | G | 1 | a0001c0001t0012 | 3 | HG03491.hp2 HG03492.hp1 HG03831.hp2 |
3_prime_UTR_variant | MODIFIER | c.*21A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 11/11 | 21 | chr8 | 108486619 | ||||||
| chr8:108486768 | A | G | 1 | a0001c0001t0025 | 1 | HG02970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*170A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 11/11 | 170 | chr8 | 108486768 | ||||||
| chr8:108486953 | A | G | 6 | a0001c0001t0002 a0001c0001t0013 a0001c0001t0029 others(3): Show |
94 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(91): Show |
3_prime_UTR_variant | MODIFIER | c.*355A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 11/11 | 355 | chr8 | 108486953 | ||||||
| chr8:108487032 | C | T | 1 | a0001c0001t0007 | 5 | HG02257.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*434C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 11/11 | 434 | chr8 | 108487032 | ||||||
| chr8:108487598 | C | T | 2 | a0001c0001t0006 a0001c0001t0019 |
12 | HG00738.hp1 HG01074.hp2 HG01255.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1000C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 11/11 | 1000 | chr8 | 108487598 | ||||||
| chr8:108487812 | C | G | 1 | a0001c0001t0031 | 1 | NA19007.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1214C>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 11/11 | 1214 | chr8 | 108487812 | ||||||
| chr8:108487825 | T | A | 1 | a0001c0001t0011 | 3 | HG01884.hp2 HG02486.hp1 HG03098.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1227T>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 11/11 | 1227 | chr8 | 108487825 | ||||||
| chr8:108487856 | C | A | 2 | a0001c0001t0008 a0001c0001t0027 |
5 | HG01261.hp2 HG02717.hp2 HG02922.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1258C>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 11/11 | 1258 | chr8 | 108487856 | ||||||
| chr8:108487884 | T | G | 10 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0006 others(7): Show |
61 | HG00733.hp2 HG00738.hp1 HG01074.hp2 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*1286T>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 11/11 | 1286 | chr8 | 108487884 | ||||||
| chr8:108487950 | G | A | 1 | a0001c0001t0029 | 1 | HG03239.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1352G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 11/11 | 1352 | chr8 | 108487950 | ||||||
| chr8:108487988 | A | G | 4 | a0001c0001t0003 a0001c0001t0024 a0001c0001t0026 others(1): Show |
57 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(54): Show |
3_prime_UTR_variant | MODIFIER | c.*1390A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 11/11 | 1390 | chr8 | 108487988 | ||||||
| chr8:108488011 | A | G | 1 | a0001c0001t0011 | 3 | HG01884.hp2 HG02486.hp1 HG03098.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1413A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 11/11 | 1413 | chr8 | 108488011 | ||||||
| chr8:108488040 | G | T | 1 | a0001c0001t0020 | 1 | HG03540.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1442G>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 11/11 | 1442 | chr8 | 108488040 | ||||||
| chr8:108488114 | A | T | 1 | a0001c0001t0017 | 2 | HG02895.hp2 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1516A>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 11/11 | 1516 | chr8 | 108488114 | ||||||
| chr8:108488144 | A | G | 1 | a0001c0001t0016 | 2 | HG02486.hp2 HG02886.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1546A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 11/11 | 1546 | chr8 | 108488144 | ||||||
| chr8:108488166 | CT | C | 23 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(20): Show |
211 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(208): Show |
3_prime_UTR_variant | MODIFIER | c.*1586delT | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 11/11 | 1586 | INFO_REALIGN_3_PRIME | chr8 | 108488166 | |||||
| chr8:108488225 | C | T | 1 | a0001c0001t0010 | 4 | HG00735.hp2 HG01099.hp2 HG01361.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1627C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 11/11 | 1627 | chr8 | 108488225 | ||||||
| chr8:108488226 | G | A | 1 | a0001c0001t0023 | 1 | NA18979.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1628G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 11/11 | 1628 | chr8 | 108488226 | ||||||
| chr8:108488245 | A | G | 3 | a0001c0001t0015 a0001c0001t0018 a0002c0003t0018 |
4 | HG01109.hp2 HG02896.hp1 HG02976.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1647A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 11/11 | 1647 | chr8 | 108488245 | ||||||
| chr8:108488559 | A | G | 1 | a0001c0001t0014 | 2 | HG01167.hp2 HG02451.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1961A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 11/11 | 1961 | chr8 | 108488559 | ||||||
| chr8:108488651 | G | A | 3 | a0001c0001t0003 a0001c0001t0026 a0001c0002t0003 |
56 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(53): Show |
3_prime_UTR_variant | MODIFIER | c.*2053G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 11/11 | 2053 | chr8 | 108488651 | ||||||
| chr8:108488802 | A | G | 17 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0007 others(14): Show |
167 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(164): Show |
3_prime_UTR_variant | MODIFIER | c.*2204A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 11/11 | 2204 | chr8 | 108488802 | ||||||
| chr8:108488914 | C | T | 1 | a0001c0001t0013 | 3 | NA18948.hp2 NA18957.hp2 NA18979.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2316C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 11/11 | 2316 | chr8 | 108488914 | ||||||
| chr8:108489135 | G | A | 1 | a0001c0001t0022 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2537G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 11/11 | 2537 | chr8 | 108489135 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:108443761 | C | T | 2 | a0001c0001t0005g0050 a0001c0001t0005g0246 |
3 | HG02451.hp1 HG02647.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.40+63C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108443761 | |||||||
| chr8:108443792 | G | T | 2 | a0001c0001t0002g0244 a0001c0001t0002g0245 |
2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.40+94G>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108443792 | |||||||
| chr8:108444155 | C | G | 5 | a0001c0001t0001g0239 a0001c0001t0001g0240 a0001c0001t0001g0241 others(2): Show |
5 | HG01106.hp1 HG01167.hp1 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.40+457C>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108444155 | |||||||
| chr8:108444175 | C | T | 5 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 others(2): Show |
8 | HG00642.hp2 HG01081.hp2 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.40+477C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108444175 | |||||||
| chr8:108444245 | C | T | 1 | a0001c0001t0028g0236 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.40+547C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108444245 | |||||||
| chr8:108444383 | A | G | 4 | a0001c0001t0001g0046 a0001c0001t0001g0233 a0001c0001t0001g0234 others(1): Show |
5 | HG02109.hp1 HG02145.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.40+685A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108444383 | |||||||
| chr8:108444436 | C | T | 2 | a0001c0001t0002g0231 a0001c0001t0030g0232 |
2 | NA18978.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.40+738C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108444436 | |||||||
| chr8:108444817 | C | G | 1 | a0001c0001t0002g0230 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.40+1119C>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108444817 | |||||||
| chr8:108444849 | A | G | 1 | a0001c0001t0001g0229 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.40+1151A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108444849 | |||||||
| chr8:108444895 | A | C | 1 | a0001c0001t0002g0228 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.40+1197A>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108444895 | |||||||
| chr8:108445147 | T | C | 1 | a0001c0001t0001g0051 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.40+1449T>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108445147 | |||||||
| chr8:108445323 | G | A | 1 | a0001c0001t0022g0052 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.40+1625G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108445323 | |||||||
| chr8:108445503 | T | C | 1 | a0001c0001t0002g0053 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.40+1805T>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108445503 | |||||||
| chr8:108445569 | C | T | 1 | a0001c0001t0001g0227 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.40+1871C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108445569 | |||||||
| chr8:108445589 | C | A | 6 | a0001c0001t0004g0054 a0001c0001t0004g0057 a0001c0001t0004g0058 others(3): Show |
6 | HG00733.hp2 HG02486.hp2 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.40+1891C>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108445589 | |||||||
| chr8:108446000 | T | A | 113 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(110): Show |
167 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.40+2302T>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108446000 | |||||||
| chr8:108446035 | C | G | 1 | a0001c0001t0001g0226 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.40+2337C>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108446035 | |||||||
| chr8:108446074 | T | C | 1 | a0001c0001t0001g0143 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.40+2376T>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108446074 | |||||||
| chr8:108446121 | A | G | 1 | a0001c0001t0015g0045 | 2 | HG02896.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.40+2423A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108446121 | |||||||
| chr8:108446379 | A | G | 1 | a0001c0001t0015g0045 | 2 | HG02896.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.40+2681A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108446379 | |||||||
| chr8:108446469 | A | C | 1 | a0001c0001t0004g0225 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.40+2771A>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108446469 | |||||||
| chr8:108446490 | TCTTCGAA others(3): Show |
T | 1 | a0001c0001t0009g0060 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.40+2807_40+2816del others(10): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr8 | 108446490 | ||||||
| chr8:108446527 | A | G | 1 | a0001c0001t0003g0028 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.40+2829A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108446527 | |||||||
| chr8:108446823 | G | A | 1 | a0001c0001t0011g0014 | 3 | HG01884.hp2 HG02486.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.41-3000G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108446823 | |||||||
| chr8:108446862 | G | A | 1 | a0001c0001t0009g0011 | 3 | HG02965.hp2 HG03540.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.41-2961G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108446862 | |||||||
| chr8:108446872 | G | A | 1 | a0001c0001t0001g0144 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.41-2951G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108446872 | |||||||
| chr8:108446923 | T | C | 1 | a0001c0001t0001g0233 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.41-2900T>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108446923 | |||||||
| chr8:108447005 | A | T | 1 | a0001c0001t0015g0045 | 2 | HG02896.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.41-2818A>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108447005 | |||||||
| chr8:108447103 | A | G | 62 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(59): Show |
94 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(91): Show |
intron_variant | MODIFIER | c.41-2720A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108447103 | |||||||
| chr8:108447109 | A | T | 1 | a0001c0001t0001g0010 | 4 | HG02280.hp1 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.41-2714A>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108447109 | |||||||
| chr8:108447211 | C | T | 3 | a0001c0001t0007g0020 a0001c0001t0007g0021 a0001c0001t0007g0100 |
5 | HG02257.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.41-2612C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108447211 | |||||||
| chr8:108447506 | A | C | 1 | a0001c0001t0003g0099 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.41-2317A>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108447506 | |||||||
| chr8:108447625 | C | T | 1 | a0001c0001t0003g0098 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.41-2198C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108447625 | |||||||
| chr8:108447687 | C | T | 1 | a0001c0001t0007g0021 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.41-2136C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108447687 | |||||||
| chr8:108447778 | A | G | 2 | a0001c0001t0001g0223 a0001c0001t0001g0224 |
2 | NA18939.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.41-2045A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108447778 | |||||||
| chr8:108447930 | T | A | 165 | a0001c0001t0001g0046 a0001c0001t0001g0233 a0001c0001t0001g0234 others(162): Show |
233 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.41-1893T>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108447930 | |||||||
| chr8:108448075 | G | A | 161 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(158): Show |
228 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.41-1748G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108448075 | |||||||
| chr8:108448193 | C | T | 1 | a0001c0001t0002g0142 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.41-1630C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108448193 | |||||||
| chr8:108448259 | C | T | 1 | a0001c0001t0028g0236 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.41-1564C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108448259 | |||||||
| chr8:108448339 | C | G | 1 | a0001c0001t0001g0222 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.41-1484C>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108448339 | |||||||
| chr8:108448425 | TGAG | T | 6 | a0001c0001t0004g0029 a0001c0001t0004g0145 a0001c0001t0004g0147 others(3): Show |
6 | HG02615.hp1 HG02717.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.41-1391_41-1389del others(3): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr8 | 108448425 | ||||||
| chr8:108448569 | G | A | 1 | a0001c0001t0001g0010 | 4 | HG02280.hp1 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.41-1254G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108448569 | |||||||
| chr8:108448670 | T | C | 1 | a0001c0001t0006g0149 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.41-1153T>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108448670 | |||||||
| chr8:108448726 | A | G | 1 | a0001c0001t0002g0141 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.41-1097A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108448726 | |||||||
| chr8:108448937 | T | G | 1 | a0001c0001t0004g0054 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.41-886T>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108448937 | |||||||
| chr8:108449016 | T | C | 1 | a0001c0001t0022g0052 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.41-807T>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449016 | |||||||
| chr8:108449192 | C | T | 2 | a0001c0001t0009g0011 a0001c0001t0009g0060 |
4 | HG02965.hp2 HG03540.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.41-631C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449192 | |||||||
| chr8:108449258 | G | A | 2 | a0001c0001t0012g0019 a0001c0001t0012g0061 |
3 | HG03491.hp2 HG03492.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.41-565G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449258 | |||||||
| chr8:108449275 | CT | C | 161 | a0001c0001t0001g0173 a0001c0001t0001g0239 a0001c0001t0002g0003 others(158): Show |
228 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.41-532delT | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr8 | 108449275 | ||||||
| chr8:108449313 | A | G | 161 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(158): Show |
228 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.41-510A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449313 | |||||||
| chr8:108449432 | T | C | 161 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(158): Show |
228 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.41-391T>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449432 | |||||||
| chr8:108449460 | A | G | 1 | a0001c0001t0028g0236 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.41-363A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449460 | |||||||
| chr8:108449469 | C | T | 1 | a0001c0001t0004g0054 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.41-354C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449469 | |||||||
| chr8:108449495 | A | C | 1 | a0001c0001t0001g0221 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.41-328A>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449495 | |||||||
| chr8:108449497 | T | G | 1 | a0001c0001t0001g0221 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.41-326T>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449497 | |||||||
| chr8:108449500 | T | C | 1 | a0001c0001t0001g0221 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.41-323T>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449500 | |||||||
| chr8:108449501 | G | A | 1 | a0001c0001t0001g0221 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.41-322G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449501 | |||||||
| chr8:108449502 | G | A | 1 | a0001c0001t0001g0221 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.41-321G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449502 | |||||||
| chr8:108449504 | T | G | 1 | a0001c0001t0001g0221 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.41-319T>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449504 | |||||||
| chr8:108449516 | C | T | 1 | a0001c0001t0001g0221 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.41-307C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449516 | |||||||
| chr8:108449519 | ACCTTGGG others(4): Show |
A | 1 | a0001c0001t0001g0221 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.41-302_41-292delCT others(9): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr8 | 108449519 | ||||||
| chr8:108449532 | A | G | 3 | a0001c0001t0007g0020 a0001c0001t0007g0021 a0001c0001t0007g0100 |
5 | HG02257.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.41-291A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449532 | |||||||
| chr8:108449533 | A | G | 1 | a0001c0001t0001g0221 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.41-290A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449533 | |||||||
| chr8:108449535 | G | C | 1 | a0001c0001t0001g0221 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.41-288G>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449535 | |||||||
| chr8:108449538 | C | A | 1 | a0001c0001t0001g0221 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.41-285C>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449538 | |||||||
| chr8:108449539 | T | A | 1 | a0001c0001t0001g0221 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.41-284T>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449539 | |||||||
| chr8:108449540 | G | T | 1 | a0001c0001t0001g0221 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.41-283G>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449540 | |||||||
| chr8:108449544 | T | A | 1 | a0001c0001t0001g0221 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.41-279T>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449544 | |||||||
| chr8:108449546 | A | T | 1 | a0001c0001t0001g0221 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.41-277A>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449546 | |||||||
| chr8:108449548 | T | C | 1 | a0001c0001t0001g0221 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.41-275T>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449548 | |||||||
| chr8:108449549 | G | C | 1 | a0001c0001t0001g0221 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.41-274G>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449549 | |||||||
| chr8:108449552 | G | C | 1 | a0001c0001t0001g0221 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.41-271G>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449552 | |||||||
| chr8:108449553 | T | A | 1 | a0001c0001t0001g0221 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.41-270T>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449553 | |||||||
| chr8:108449556 | G | A | 1 | a0001c0001t0001g0221 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.41-267G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449556 | |||||||
| chr8:108449560 | C | T | 1 | a0001c0001t0001g0221 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.41-263C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449560 | |||||||
| chr8:108449561 | C | T | 1 | a0001c0001t0002g0053 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.41-262C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449561 | |||||||
| chr8:108449562 | G | A | 1 | a0001c0001t0001g0221 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.41-261G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449562 | |||||||
| chr8:108449564 | G | C | 1 | a0001c0001t0001g0221 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.41-259G>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449564 | |||||||
| chr8:108449565 | C | A | 1 | a0001c0001t0001g0221 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.41-258C>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449565 | |||||||
| chr8:108449566 | C | T | 1 | a0001c0001t0001g0221 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.41-257C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449566 | |||||||
| chr8:108449568 | G | T | 1 | a0001c0001t0001g0221 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.41-255G>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449568 | |||||||
| chr8:108449569 | G | T | 1 | a0001c0001t0001g0221 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.41-254G>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449569 | |||||||
| chr8:108449570 | C | T | 1 | a0001c0001t0001g0221 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.41-253C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449570 | |||||||
| chr8:108449571 | C | T | 1 | a0001c0001t0001g0221 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.41-252C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449571 | |||||||
| chr8:108449578 | T | G | 1 | a0001c0001t0001g0221 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.41-245T>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449578 | |||||||
| chr8:108449579 | C | A | 1 | a0001c0001t0001g0221 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.41-244C>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449579 | |||||||
| chr8:108449583 | T | A | 1 | a0001c0001t0001g0221 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.41-240T>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449583 | |||||||
| chr8:108449584 | C | G | 1 | a0001c0001t0001g0221 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.41-239C>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449584 | |||||||
| chr8:108449585 | T | A | 1 | a0001c0001t0001g0221 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.41-238T>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449585 | |||||||
| chr8:108449589 | G | A | 1 | a0001c0001t0001g0221 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.41-234G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449589 | |||||||
| chr8:108449591 | T | C | 1 | a0001c0001t0001g0221 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.41-232T>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449591 | |||||||
| chr8:108449593 | G | A | 1 | a0001c0001t0001g0221 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.41-230G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449593 | |||||||
| chr8:108449596 | A | C | 1 | a0001c0001t0001g0221 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.41-227A>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449596 | |||||||
| chr8:108449600 | T | A | 1 | a0001c0001t0001g0221 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.41-223T>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449600 | |||||||
| chr8:108449602 | C | T | 1 | a0001c0001t0001g0221 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.41-221C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449602 | |||||||
| chr8:108449603 | C | T | 1 | a0001c0001t0001g0221 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.41-220C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449603 | |||||||
| chr8:108449604 | A | T | 1 | a0001c0001t0001g0221 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.41-219A>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449604 | |||||||
| chr8:108449605 | G | A | 1 | a0001c0001t0001g0221 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.41-218G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449605 | |||||||
| chr8:108449607 | T | A | 1 | a0001c0001t0001g0221 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.41-216T>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449607 | |||||||
| chr8:108449608 | G | T | 1 | a0001c0001t0001g0221 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.41-215G>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449608 | |||||||
| chr8:108449609 | T | G | 1 | a0001c0001t0001g0221 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.41-214T>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449609 | |||||||
| chr8:108449612 | T | A | 1 | a0001c0001t0001g0221 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.41-211T>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449612 | |||||||
| chr8:108449615 | T | A | 1 | a0001c0001t0001g0221 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.41-208T>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449615 | |||||||
| chr8:108449616 | G | A | 1 | a0001c0001t0001g0221 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.41-207G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449616 | |||||||
| chr8:108449617 | T | A | 1 | a0001c0001t0001g0221 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.41-206T>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449617 | |||||||
| chr8:108449618 | T | A | 1 | a0001c0001t0001g0221 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.41-205T>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449618 | |||||||
| chr8:108449619 | T | A | 1 | a0001c0001t0001g0221 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.41-204T>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449619 | |||||||
| chr8:108449623 | T | C | 1 | a0001c0001t0001g0221 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.41-200T>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449623 | |||||||
| chr8:108449625 | T | C | 1 | a0001c0001t0001g0221 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.41-198T>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449625 | |||||||
| chr8:108449626 | T | A | 1 | a0001c0001t0001g0221 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.41-197T>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449626 | |||||||
| chr8:108449628 | T | A | 1 | a0001c0001t0001g0221 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.41-195T>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449628 | |||||||
| chr8:108449633 | G | A | 1 | a0001c0001t0001g0221 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.41-190G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449633 | |||||||
| chr8:108449635 | T | A | 1 | a0001c0001t0001g0221 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.41-188T>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449635 | |||||||
| chr8:108449637 | T | A | 1 | a0001c0001t0001g0221 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.41-186T>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449637 | |||||||
| chr8:108449638 | G | A | 1 | a0001c0001t0001g0221 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.41-185G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449638 | |||||||
| chr8:108449642 | C | A | 1 | a0001c0001t0001g0221 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.41-181C>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449642 | |||||||
| chr8:108449645 | T | A | 1 | a0001c0001t0001g0221 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.41-178T>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449645 | |||||||
| chr8:108449646 | T | A | 1 | a0001c0001t0001g0221 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.41-177T>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449646 | |||||||
| chr8:108449652 | A | G | 161 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(158): Show |
228 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.41-171A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449652 | |||||||
| chr8:108449653 | T | A | 1 | a0001c0001t0001g0221 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.41-170T>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449653 | |||||||
| chr8:108449656 | A | C | 1 | a0001c0001t0001g0221 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.41-167A>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449656 | |||||||
| chr8:108449657 | T | A | 1 | a0001c0001t0001g0221 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.41-166T>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449657 | |||||||
| chr8:108449660 | T | C | 1 | a0001c0001t0001g0221 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.41-163T>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449660 | |||||||
| chr8:108449662 | T | C | 1 | a0001c0001t0001g0221 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.41-161T>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449662 | |||||||
| chr8:108449664 | C | CCAACAGT others(5): Show |
1 | a0001c0001t0001g0221 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.41-159_41-158insCA others(10): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449664 | |||||||
| chr8:108449669 | T | G | 1 | a0001c0001t0001g0221 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.41-154T>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449669 | |||||||
| chr8:108449670 | C | T | 1 | a0001c0001t0001g0221 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.41-153C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449670 | |||||||
| chr8:108449703 | G | T | 4 | a0001c0001t0008g0217 a0001c0001t0008g0218 a0001c0001t0008g0219 others(1): Show |
4 | HG02717.hp2 HG02922.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.41-120G>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 1/10 | chr8 | 108449703 | |||||||
| chr8:108449945 | T | C | 1 | a0001c0001t0001g0240 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.154+9T>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 2/10 | chr8 | 108449945 | |||||||
| chr8:108449986 | C | CT | 5 | a0001c0001t0001g0010 a0001c0001t0005g0034 a0001c0001t0005g0050 others(2): Show |
10 | HG01243.hp2 HG02280.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.154+63dupT | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr8 | 108449986 | ||||||
| chr8:108450045 | C | G | 1 | a0001c0001t0027g0216 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.154+109C>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 2/10 | chr8 | 108450045 | |||||||
| chr8:108450135 | A | C | 2 | a0001c0001t0005g0050 a0001c0001t0005g0246 |
3 | HG02451.hp1 HG02647.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.154+199A>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 2/10 | chr8 | 108450135 | |||||||
| chr8:108450140 | G | T | 2 | a0001c0001t0005g0050 a0001c0001t0005g0246 |
3 | HG02451.hp1 HG02647.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.154+204G>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 2/10 | chr8 | 108450140 | |||||||
| chr8:108450400 | G | A | 2 | a0001c0001t0001g0174 a0001c0001t0001g0175 |
2 | HG02622.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.155-28G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 2/10 | chr8 | 108450400 | |||||||
| chr8:108450516 | A | G | 1 | a0001c0001t0003g0096 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.219+24A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 3/10 | chr8 | 108450516 | |||||||
| chr8:108450539 | A | C | 1 | a0001c0001t0004g0148 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.219+47A>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 3/10 | chr8 | 108450539 | |||||||
| chr8:108450562 | A | G | 161 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(158): Show |
228 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.219+70A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 3/10 | chr8 | 108450562 | |||||||
| chr8:108450606 | T | C | 1 | a0001c0001t0001g0174 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.219+114T>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 3/10 | chr8 | 108450606 | |||||||
| chr8:108450794 | G | A | 2 | a0001c0001t0002g0101 a0001c0001t0002g0140 |
2 | NA18959.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.219+302G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 3/10 | chr8 | 108450794 | |||||||
| chr8:108450837 | A | G | 1 | a0001c0001t0004g0171 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.219+345A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 3/10 | chr8 | 108450837 | |||||||
| chr8:108450922 | C | T | 32 | a0001c0001t0004g0015 a0001c0001t0004g0029 a0001c0001t0004g0030 others(29): Show |
40 | HG00738.hp1 HG01074.hp2 HG01167.hp2 others(37): Show |
intron_variant | MODIFIER | c.219+430C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 3/10 | chr8 | 108450922 | |||||||
| chr8:108451016 | A | G | 1 | a0001c0001t0002g0139 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.219+524A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 3/10 | chr8 | 108451016 | |||||||
| chr8:108451215 | G | A | 1 | a0001c0001t0011g0014 | 3 | HG01884.hp2 HG02486.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.219+723G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 3/10 | chr8 | 108451215 | |||||||
| chr8:108451215 | GA | G | 126 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(123): Show |
183 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.219+730delA | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr8 | 108451215 | ||||||
| chr8:108451216 | A | G | 3 | a0001c0001t0002g0138 a0001c0001t0004g0059 a0001c0001t0011g0014 |
5 | HG00733.hp2 HG01884.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.219+724A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 3/10 | chr8 | 108451216 | |||||||
| chr8:108451219 | AAAATC | A | 32 | a0001c0001t0004g0015 a0001c0001t0004g0029 a0001c0001t0004g0030 others(29): Show |
40 | HG00738.hp1 HG01074.hp2 HG01167.hp2 others(37): Show |
intron_variant | MODIFIER | c.219+731_219+735del others(5): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr8 | 108451219 | ||||||
| chr8:108451243 | T | C | 2 | a0001c0001t0018g0062 a0002c0003t0018g0063 |
2 | HG01109.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.219+751T>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 3/10 | chr8 | 108451243 | |||||||
| chr8:108451308 | TTACATCA others(359): Show |
T | 1 | a0001c0001t0015g0045 | 2 | HG02896.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.219+817_219+1182de others(1): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 3/10 | chr8 | 108451308 | |||||||
| chr8:108451568 | A | T | 2 | a0001c0001t0005g0050 a0001c0001t0005g0246 |
3 | HG02451.hp1 HG02647.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.219+1076A>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 3/10 | chr8 | 108451568 | |||||||
| chr8:108451675 | C | G | 6 | a0001c0001t0005g0034 a0001c0001t0005g0150 a0001c0001t0005g0151 others(3): Show |
7 | HG01243.hp2 HG02055.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.219+1183C>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 3/10 | chr8 | 108451675 | |||||||
| chr8:108451676 | G | GT | 113 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(110): Show |
167 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.219+1188dupT | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr8 | 108451676 | ||||||
| chr8:108451883 | A | C | 2 | a0001c0001t0014g0169 a0001c0001t0014g0170 |
2 | HG01167.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.220-1179A>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 3/10 | chr8 | 108451883 | |||||||
| chr8:108451990 | T | G | 113 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(110): Show |
167 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.220-1072T>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 3/10 | chr8 | 108451990 | |||||||
| chr8:108452053 | T | A | 4 | a0001c0001t0001g0046 a0001c0001t0001g0233 a0001c0001t0001g0234 others(1): Show |
5 | HG02109.hp1 HG02145.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.220-1009T>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 3/10 | chr8 | 108452053 | |||||||
| chr8:108452073 | G | T | 49 | a0001c0001t0003g0002 a0001c0001t0003g0006 a0001c0001t0003g0012 others(46): Show |
71 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(68): Show |
intron_variant | MODIFIER | c.220-989G>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 3/10 | chr8 | 108452073 | |||||||
| chr8:108452186 | A | G | 161 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(158): Show |
228 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.220-876A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 3/10 | chr8 | 108452186 | |||||||
| chr8:108452206 | G | A | 161 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(158): Show |
228 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.220-856G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 3/10 | chr8 | 108452206 | |||||||
| chr8:108452251 | A | G | 1 | a0001c0001t0022g0052 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.220-811A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 3/10 | chr8 | 108452251 | |||||||
| chr8:108452342 | G | A | 1 | a0001c0001t0007g0100 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.220-720G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 3/10 | chr8 | 108452342 | |||||||
| chr8:108452396 | G | A | 2 | a0001c0001t0016g0055 a0001c0001t0016g0056 |
2 | HG02486.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.220-666G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 3/10 | chr8 | 108452396 | |||||||
| chr8:108452425 | G | T | 1 | a0001c0001t0001g0018 | 3 | NA18963.hp2 NA19004.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.220-637G>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 3/10 | chr8 | 108452425 | |||||||
| chr8:108452914 | A | G | 4 | a0001c0001t0003g0012 a0001c0001t0003g0094 a0001c0001t0003g0095 others(1): Show |
6 | HG00099.hp1 HG00741.hp2 HG01069.hp1 others(3): Show |
intron_variant | MODIFIER | c.220-148A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 3/10 | chr8 | 108452914 | |||||||
| chr8:108453268 | T | G | 1 | a0001c0001t0003g0064 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.305+121T>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 4/10 | chr8 | 108453268 | |||||||
| chr8:108453318 | A | C | 1 | a0001c0001t0015g0045 | 2 | HG02896.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.305+171A>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 4/10 | chr8 | 108453318 | |||||||
| chr8:108453407 | T | C | 1 | a0001c0001t0020g0154 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.305+260T>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 4/10 | chr8 | 108453407 | |||||||
| chr8:108453469 | C | T | 4 | a0001c0001t0001g0046 a0001c0001t0001g0233 a0001c0001t0001g0234 others(1): Show |
5 | HG02109.hp1 HG02145.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.305+322C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 4/10 | chr8 | 108453469 | |||||||
| chr8:108453503 | A | G | 1 | a0001c0001t0005g0153 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.305+356A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 4/10 | chr8 | 108453503 | |||||||
| chr8:108453582 | T | C | 1 | a0001c0001t0018g0062 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.305+435T>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 4/10 | chr8 | 108453582 | |||||||
| chr8:108453700 | T | C | 161 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(158): Show |
228 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.305+553T>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 4/10 | chr8 | 108453700 | |||||||
| chr8:108453864 | C | T | 1 | a0001c0001t0020g0154 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.305+717C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 4/10 | chr8 | 108453864 | |||||||
| chr8:108453866 | A | G | 7 | a0001c0001t0004g0054 a0001c0001t0004g0057 a0001c0001t0004g0058 others(4): Show |
8 | HG00733.hp2 HG02486.hp2 HG02683.hp2 others(5): Show |
intron_variant | MODIFIER | c.305+719A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 4/10 | chr8 | 108453866 | |||||||
| chr8:108453949 | C | T | 2 | a0001c0001t0002g0013 a0001c0001t0002g0136 |
4 | NA18939.hp2 NA19001.hp2 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.305+802C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 4/10 | chr8 | 108453949 | |||||||
| chr8:108454033 | T | A | 2 | a0001c0001t0018g0062 a0002c0003t0018g0063 |
2 | HG01109.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.305+886T>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 4/10 | chr8 | 108454033 | |||||||
| chr8:108454355 | C | T | 111 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(108): Show |
165 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.305+1208C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 4/10 | chr8 | 108454355 | |||||||
| chr8:108454428 | A | G | 1 | a0001c0001t0001g0010 | 4 | HG02280.hp1 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.305+1281A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 4/10 | chr8 | 108454428 | |||||||
| chr8:108454466 | A | G | 2 | a0001c0001t0010g0214 a0001c0001t0010g0215 |
2 | HG01099.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.305+1319A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 4/10 | chr8 | 108454466 | |||||||
| chr8:108454932 | C | G | 7 | a0001c0001t0004g0054 a0001c0001t0004g0057 a0001c0001t0004g0058 others(4): Show |
8 | HG00733.hp2 HG02486.hp2 HG02683.hp2 others(5): Show |
intron_variant | MODIFIER | c.306-941C>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 4/10 | chr8 | 108454932 | |||||||
| chr8:108454983 | T | C | 6 | a0001c0001t0004g0054 a0001c0001t0004g0057 a0001c0001t0004g0058 others(3): Show |
6 | HG00733.hp2 HG02486.hp2 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.306-890T>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 4/10 | chr8 | 108454983 | |||||||
| chr8:108455040 | G | C | 113 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(110): Show |
167 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.306-833G>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 4/10 | chr8 | 108455040 | |||||||
| chr8:108455215 | C | T | 161 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(158): Show |
228 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.306-658C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 4/10 | chr8 | 108455215 | |||||||
| chr8:108455266 | A | G | 1 | a0001c0001t0015g0045 | 2 | HG02896.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.306-607A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 4/10 | chr8 | 108455266 | |||||||
| chr8:108455285 | A | C | 1 | a0001c0001t0023g0213 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.306-588A>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 4/10 | chr8 | 108455285 | |||||||
| chr8:108455400 | T | C | 1 | a0001c0001t0003g0066 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.306-473T>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 4/10 | chr8 | 108455400 | |||||||
| chr8:108455639 | T | G | 1 | a0001c0001t0002g0102 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.306-234T>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 4/10 | chr8 | 108455639 | |||||||
| chr8:108455718 | G | A | 1 | a0001c0001t0004g0155 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.306-155G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 4/10 | chr8 | 108455718 | |||||||
| chr8:108455733 | C | T | 39 | a0001c0001t0003g0002 a0001c0001t0003g0006 a0001c0001t0003g0012 others(36): Show |
56 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(53): Show |
intron_variant | MODIFIER | c.306-140C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 4/10 | chr8 | 108455733 | |||||||
| chr8:108455825 | A | G | 1 | a0001c0001t0004g0171 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.306-48A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 4/10 | chr8 | 108455825 | |||||||
| chr8:108456001 | T | TAGAA | 161 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(158): Show |
228 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.363+74_363+75insAA others(2): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 108456001 | ||||||
| chr8:108456078 | A | G | 2 | a0001c0001t0009g0011 a0001c0001t0009g0060 |
4 | HG02965.hp2 HG03540.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.363+148A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108456078 | |||||||
| chr8:108456088 | A | G | 1 | a0001c0001t0003g0093 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.363+158A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108456088 | |||||||
| chr8:108456097 | T | G | 1 | a0001c0001t0002g0103 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.363+167T>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108456097 | |||||||
| chr8:108456139 | C | A | 1 | a0001c0001t0001g0176 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.363+209C>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108456139 | |||||||
| chr8:108456193 | T | C | 161 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(158): Show |
228 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.363+263T>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108456193 | |||||||
| chr8:108456194 | G | A | 1 | a0001c0001t0003g0068 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.363+264G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108456194 | |||||||
| chr8:108456228 | G | T | 1 | a0001c0001t0003g0095 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.363+298G>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108456228 | |||||||
| chr8:108456332 | C | CA | 9 | a0001c0001t0004g0030 a0001c0001t0004g0155 a0001c0001t0004g0156 others(6): Show |
10 | HG01243.hp1 HG02258.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.363+417dupA | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 108456332 | ||||||
| chr8:108456332 | C | CAAAAAAA others(13): Show |
1 | a0001c0001t0004g0058 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.363+417_363+418ins others(20): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 108456332 | ||||||
| chr8:108456332 | C | CAAAAAAA others(20): Show |
1 | a0001c0001t0004g0057 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.363+417_363+418ins others(27): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 108456332 | ||||||
| chr8:108456344 | AAAAG | A | 99 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(96): Show |
142 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(139): Show |
intron_variant | MODIFIER | c.363+418_363+421del others(4): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 108456344 | ||||||
| chr8:108456345 | AAAG | A | 22 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(19): Show |
25 | HG00140.hp2 HG00438.hp2 HG00609.hp1 others(22): Show |
intron_variant | MODIFIER | c.363+418_363+420del others(3): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 108456345 | ||||||
| chr8:108456347 | AG | A | 6 | a0001c0001t0004g0015 a0001c0001t0005g0034 a0001c0001t0005g0150 others(3): Show |
10 | HG01243.hp2 HG01884.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.363+418delG | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108456347 | |||||||
| chr8:108456348 | G | A | 41 | a0001c0001t0001g0212 a0001c0001t0004g0015 a0001c0001t0004g0029 others(38): Show |
48 | HG00738.hp1 HG01074.hp2 HG01167.hp2 others(45): Show |
intron_variant | MODIFIER | c.363+418G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108456348 | |||||||
| chr8:108456349 | A | G | 1 | a0001c0001t0001g0212 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.363+419A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108456349 | |||||||
| chr8:108456359 | A | AAAAAAAA others(6): Show |
1 | a0001c0001t0016g0055 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.363+431_363+432ins others(13): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 108456359 | ||||||
| chr8:108456359 | A | AAAAAAAA others(5): Show |
1 | a0001c0001t0016g0056 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.363+431_363+432ins others(12): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 108456359 | ||||||
| chr8:108456362 | C | A | 1 | a0001c0001t0002g0104 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.363+432C>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108456362 | |||||||
| chr8:108456463 | A | G | 113 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(110): Show |
167 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.363+533A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108456463 | |||||||
| chr8:108456646 | G | A | 2 | a0001c0001t0005g0050 a0001c0001t0005g0246 |
3 | HG02451.hp1 HG02647.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.363+716G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108456646 | |||||||
| chr8:108456682 | G | A | 3 | a0001c0001t0003g0006 a0001c0001t0003g0069 a0001c0001t0003g0070 |
6 | HG01891.hp2 HG02109.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.363+752G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108456682 | |||||||
| chr8:108456843 | C | T | 48 | a0001c0001t0004g0015 a0001c0001t0004g0029 a0001c0001t0004g0030 others(45): Show |
61 | HG00733.hp2 HG00738.hp1 HG01074.hp2 others(58): Show |
intron_variant | MODIFIER | c.363+913C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108456843 | |||||||
| chr8:108456846 | C | T | 6 | a0001c0001t0004g0054 a0001c0001t0004g0057 a0001c0001t0004g0058 others(3): Show |
6 | HG00733.hp2 HG02486.hp2 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.363+916C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108456846 | |||||||
| chr8:108456924 | A | G | 1 | a0001c0001t0006g0168 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.363+994A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108456924 | |||||||
| chr8:108457130 | A | G | 1 | a0001c0001t0004g0167 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.363+1200A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108457130 | |||||||
| chr8:108457267 | A | G | 1 | a0001c0001t0001g0051 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.363+1337A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108457267 | |||||||
| chr8:108457303 | G | A | 1 | a0001c0001t0003g0099 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.363+1373G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108457303 | |||||||
| chr8:108457321 | CGTGTGTG others(13): Show |
C | 1 | a0001c0001t0002g0027 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.363+1401_363+1420d others(22): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 108457321 | ||||||
| chr8:108457321 | CGTGTGTG others(15): Show |
C | 8 | a0001c0001t0002g0008 a0001c0001t0002g0130 a0001c0001t0002g0131 others(5): Show |
11 | HG00738.hp2 HG01081.hp1 HG01123.hp2 others(8): Show |
intron_variant | MODIFIER | c.363+1401_363+1422d others(24): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 108457321 | ||||||
| chr8:108457331 | C | CGT | 51 | a0001c0001t0001g0009 a0001c0001t0001g0039 a0001c0001t0001g0051 others(48): Show |
78 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(75): Show |
intron_variant | MODIFIER | c.363+1442_363+1443d others(4): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 108457331 | ||||||
| chr8:108457331 | C | CGTGT | 12 | a0001c0001t0001g0001 a0001c0001t0001g0037 a0001c0001t0001g0174 others(9): Show |
15 | HG00140.hp1 HG00323.hp1 HG01255.hp1 others(12): Show |
intron_variant | MODIFIER | c.363+1440_363+1443d others(6): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 108457331 | ||||||
| chr8:108457331 | C | CGTGTGT | 5 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0002g0228 others(2): Show |
5 | HG02004.hp1 HG02258.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.363+1438_363+1443d others(8): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 108457331 | ||||||
| chr8:108457331 | CGT | C | 34 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0041 others(31): Show |
42 | HG00438.hp1 HG00639.hp1 HG01074.hp1 others(39): Show |
intron_variant | MODIFIER | c.363+1442_363+1443d others(4): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 108457331 | ||||||
| chr8:108457331 | CGTGT | C | 20 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0239 others(17): Show |
22 | HG00733.hp2 HG01106.hp1 HG01167.hp1 others(19): Show |
intron_variant | MODIFIER | c.363+1440_363+1443d others(6): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 108457331 | ||||||
| chr8:108457331 | CGTGTGT | C | 12 | a0001c0001t0001g0048 a0001c0001t0001g0198 a0001c0001t0003g0093 others(9): Show |
15 | HG00280.hp1 HG00280.hp2 HG00423.hp2 others(12): Show |
intron_variant | MODIFIER | c.363+1438_363+1443d others(8): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 108457331 | ||||||
| chr8:108457331 | CGTGTGTG others(1): Show |
C | 41 | a0001c0001t0001g0040 a0001c0001t0001g0233 a0001c0001t0003g0002 others(38): Show |
58 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.363+1436_363+1443d others(10): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 108457331 | ||||||
| chr8:108457331 | CGTGTGTG others(5): Show |
C | 1 | a0001c0001t0015g0045 | 2 | HG02896.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.363+1432_363+1443d others(14): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 108457331 | ||||||
| chr8:108457331 | CGTGTGTG others(9): Show |
C | 2 | a0001c0001t0002g0114 a0001c0001t0019g0033 |
3 | HG03688.hp1 NA19058.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.363+1428_363+1443d others(18): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 108457331 | ||||||
| chr8:108457364 | GTGTGTGT others(26): Show |
G | 1 | a0001c0001t0003g0071 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.363+1438_363+1470d others(35): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 108457364 | ||||||
| chr8:108457403 | A | G | 1 | a0001c0001t0003g0070 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.363+1473A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108457403 | |||||||
| chr8:108457426 | A | G | 161 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(158): Show |
228 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.363+1496A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108457426 | |||||||
| chr8:108457654 | G | A | 1 | a0001c0001t0001g0018 | 3 | NA18963.hp2 NA19004.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.363+1724G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108457654 | |||||||
| chr8:108457703 | C | T | 4 | a0001c0001t0001g0044 a0001c0001t0001g0221 a0001c0001t0001g0223 others(1): Show |
5 | HG00735.hp1 NA18939.hp1 NA18977.hp1 others(2): Show |
intron_variant | MODIFIER | c.363+1773C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108457703 | |||||||
| chr8:108457715 | T | A | 1 | a0001c0001t0001g0177 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.363+1785T>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108457715 | |||||||
| chr8:108457804 | T | C | 165 | a0001c0001t0001g0046 a0001c0001t0001g0233 a0001c0001t0001g0234 others(162): Show |
233 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.363+1874T>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108457804 | |||||||
| chr8:108457923 | T | C | 2 | a0001c0001t0004g0156 a0001c0001t0004g0157 |
2 | NA19030.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.363+1993T>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108457923 | |||||||
| chr8:108458026 | G | A | 1 | a0001c0001t0014g0169 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.363+2096G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108458026 | |||||||
| chr8:108458300 | C | T | 48 | a0001c0001t0004g0015 a0001c0001t0004g0029 a0001c0001t0004g0030 others(45): Show |
61 | HG00733.hp2 HG00738.hp1 HG01074.hp2 others(58): Show |
intron_variant | MODIFIER | c.363+2370C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108458300 | |||||||
| chr8:108458318 | A | G | 1 | a0001c0001t0005g0152 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.363+2388A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108458318 | |||||||
| chr8:108458370 | C | T | 1 | a0001c0001t0001g0211 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.363+2440C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108458370 | |||||||
| chr8:108458419 | G | A | 24 | a0001c0001t0004g0015 a0001c0001t0004g0029 a0001c0001t0004g0030 others(21): Show |
28 | HG01167.hp2 HG01243.hp1 HG01261.hp1 others(25): Show |
intron_variant | MODIFIER | c.363+2489G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108458419 | |||||||
| chr8:108458660 | T | A | 161 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(158): Show |
228 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.363+2730T>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108458660 | |||||||
| chr8:108458664 | C | T | 1 | a0001c0001t0001g0210 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.363+2734C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108458664 | |||||||
| chr8:108458665 | G | A | 1 | a0001c0001t0001g0234 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.363+2735G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108458665 | |||||||
| chr8:108458752 | A | G | 113 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(110): Show |
167 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.363+2822A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108458752 | |||||||
| chr8:108458832 | T | C | 4 | a0001c0001t0001g0046 a0001c0001t0001g0233 a0001c0001t0001g0234 others(1): Show |
5 | HG02109.hp1 HG02145.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.363+2902T>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108458832 | |||||||
| chr8:108458927 | G | A | 30 | a0001c0001t0003g0002 a0001c0001t0003g0012 a0001c0001t0003g0028 others(27): Show |
44 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(41): Show |
intron_variant | MODIFIER | c.363+2997G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108458927 | |||||||
| chr8:108458973 | A | C | 161 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(158): Show |
228 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.363+3043A>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108458973 | |||||||
| chr8:108459109 | C | G | 1 | a0001c0001t0022g0052 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.363+3179C>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108459109 | |||||||
| chr8:108459265 | T | G | 1 | a0001c0001t0001g0178 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.363+3335T>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108459265 | |||||||
| chr8:108459286 | C | T | 48 | a0001c0001t0004g0015 a0001c0001t0004g0029 a0001c0001t0004g0030 others(45): Show |
61 | HG00733.hp2 HG00738.hp1 HG01074.hp2 others(58): Show |
intron_variant | MODIFIER | c.363+3356C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108459286 | |||||||
| chr8:108459345 | G | C | 161 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(158): Show |
228 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.363+3415G>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108459345 | |||||||
| chr8:108459545 | A | G | 161 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(158): Show |
228 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.363+3615A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108459545 | |||||||
| chr8:108459680 | G | A | 63 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(60): Show |
95 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.363+3750G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108459680 | |||||||
| chr8:108459703 | T | TGA | 9 | a0001c0001t0001g0183 a0001c0001t0005g0246 a0001c0001t0006g0016 others(6): Show |
13 | HG00738.hp1 HG01074.hp2 HG01255.hp2 others(10): Show |
intron_variant | MODIFIER | c.363+3791_363+3792d others(4): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 108459703 | ||||||
| chr8:108459703 | T | TGAGA | 68 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(65): Show |
111 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(108): Show |
intron_variant | MODIFIER | c.363+3789_363+3792d others(6): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 108459703 | ||||||
| chr8:108459703 | T | TGAGAGA | 10 | a0001c0001t0002g0004 a0001c0001t0002g0109 a0001c0001t0002g0110 others(7): Show |
16 | HG00558.hp1 HG00609.hp1 HG01515.hp1 others(13): Show |
intron_variant | MODIFIER | c.363+3787_363+3792d others(8): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 108459703 | ||||||
| chr8:108459703 | T | TGAGAGAG others(1): Show |
44 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0007 others(41): Show |
70 | HG00438.hp2 HG00621.hp1 HG00621.hp2 others(67): Show |
intron_variant | MODIFIER | c.363+3785_363+3792d others(10): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 108459703 | ||||||
| chr8:108459703 | T | TGAGAGAG others(3): Show |
17 | a0001c0001t0001g0046 a0001c0001t0001g0233 a0001c0001t0001g0234 others(14): Show |
19 | HG00733.hp2 HG01192.hp2 HG01433.hp2 others(16): Show |
intron_variant | MODIFIER | c.363+3783_363+3792d others(12): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 108459703 | ||||||
| chr8:108459703 | T | TGAGAGAG others(5): Show |
1 | a0001c0001t0002g0105 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.363+3781_363+3792d others(14): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 108459703 | ||||||
| chr8:108459721 | A | AGAGAGAG others(9): Show |
1 | a0001c0001t0004g0167 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.363+3792_363+3793i others(18): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 108459721 | ||||||
| chr8:108459721 | A | AGAGAGAG others(11): Show |
1 | a0001c0001t0015g0045 | 2 | HG02896.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.363+3792_363+3793i others(20): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 108459721 | ||||||
| chr8:108459721 | A | AGAGAGAG others(5): Show |
4 | a0001c0001t0004g0145 a0001c0001t0005g0034 a0001c0001t0005g0153 others(1): Show |
5 | HG01243.hp2 HG02615.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.363+3792_363+3793i others(14): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 108459721 | ||||||
| chr8:108459721 | A | AGAGAGAG others(3): Show |
2 | a0001c0001t0011g0014 a0001c0001t0020g0154 |
4 | HG01884.hp2 HG02486.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.363+3792_363+3793i others(12): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 108459721 | ||||||
| chr8:108459721 | A | AGAGAGAG others(5): Show |
8 | a0001c0001t0004g0015 a0001c0001t0004g0029 a0001c0001t0004g0148 others(5): Show |
10 | HG01243.hp1 HG01261.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.363+3792_363+3793i others(14): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 108459721 | ||||||
| chr8:108459721 | A | AGAGAGAG others(7): Show |
8 | a0001c0001t0004g0030 a0001c0001t0004g0031 a0001c0001t0004g0155 others(5): Show |
10 | HG01167.hp2 HG02145.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.363+3792_363+3793i others(16): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 108459721 | ||||||
| chr8:108459721 | A | AGAGAGAG others(9): Show |
1 | a0001c0001t0009g0011 | 3 | HG02965.hp2 HG03540.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.363+3792_363+3793i others(18): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 108459721 | ||||||
| chr8:108459721 | A | AGAGAGAG others(1): Show |
29 | a0001c0001t0003g0002 a0001c0001t0003g0006 a0001c0001t0003g0012 others(26): Show |
46 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(43): Show |
intron_variant | MODIFIER | c.363+3792_363+3793i others(10): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 108459721 | ||||||
| chr8:108459721 | A | AGAGAGAG others(3): Show |
8 | a0001c0001t0003g0065 a0001c0001t0003g0069 a0001c0001t0003g0084 others(5): Show |
10 | HG02257.hp1 HG02896.hp2 HG02897.hp1 others(7): Show |
intron_variant | MODIFIER | c.363+3792_363+3793i others(12): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 108459721 | ||||||
| chr8:108459721 | A | AGAGAGAG others(5): Show |
3 | a0001c0001t0012g0019 a0001c0001t0014g0170 a0001c0001t0028g0236 |
4 | HG02451.hp2 HG03491.hp2 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.363+3792_363+3793i others(14): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 108459721 | ||||||
| chr8:108459721 | A | AGAGAGAG others(7): Show |
2 | a0001c0001t0009g0060 a0001c0001t0024g0067 |
2 | HG02630.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.363+3792_363+3793i others(16): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 108459721 | ||||||
| chr8:108459721 | A | AGAGAGAG others(11): Show |
1 | a0001c0001t0004g0171 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.363+3792_363+3793i others(20): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 108459721 | ||||||
| chr8:108459721 | A | AGAGAGT | 12 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0049 others(9): Show |
15 | HG01106.hp1 HG01256.hp1 HG01934.hp2 others(12): Show |
intron_variant | MODIFIER | c.363+3792_363+3793i others(8): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 108459721 | ||||||
| chr8:108459721 | A | AGAGAGTG others(1): Show |
3 | a0001c0001t0001g0043 a0001c0001t0001g0204 a0001c0001t0012g0061 |
4 | HG03831.hp2 NA18981.hp1 NA18993.hp1 others(1): Show |
intron_variant | MODIFIER | c.363+3792_363+3793i others(10): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 108459721 | ||||||
| chr8:108459721 | A | AGAGT | 4 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0003g0087 others(1): Show |
4 | HG01256.hp2 HG01258.hp2 HG02055.hp1 others(1): Show |
intron_variant | MODIFIER | c.363+3792_363+3793i others(6): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 108459721 | ||||||
| chr8:108459721 | A | T | 1 | a0001c0001t0004g0147 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.363+3791A>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108459721 | |||||||
| chr8:108459721 | AGT | A | 3 | a0001c0001t0004g0158 a0001c0001t0018g0062 a0002c0003t0018g0063 |
3 | HG01109.hp2 HG02572.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.363+3823_363+3824d others(4): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 108459721 | ||||||
| chr8:108459723 | T | A | 79 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0183 others(76): Show |
115 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(112): Show |
intron_variant | MODIFIER | c.363+3793T>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108459723 | |||||||
| chr8:108459725 | T | A | 64 | a0001c0001t0001g0180 a0001c0001t0002g0003 a0001c0001t0002g0004 others(61): Show |
98 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.363+3795T>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108459725 | |||||||
| chr8:108459727 | T | A | 5 | a0001c0001t0002g0106 a0001c0001t0002g0109 a0001c0001t0002g0110 others(2): Show |
5 | HG00544.hp1 HG02129.hp2 HG02155.hp2 others(2): Show |
intron_variant | MODIFIER | c.363+3797T>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108459727 | |||||||
| chr8:108459729 | T | A | 1 | a0001c0001t0004g0158 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.363+3799T>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108459729 | |||||||
| chr8:108459731 | T | A | 1 | a0001c0001t0004g0158 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.363+3801T>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108459731 | |||||||
| chr8:108459753 | T | A | 2 | a0001c0001t0001g0181 a0001c0001t0001g0182 |
2 | NA18947.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.363+3823T>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108459753 | |||||||
| chr8:108459769 | G | C | 1 | a0001c0001t0002g0130 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.363+3839G>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108459769 | |||||||
| chr8:108459850 | A | G | 3 | a0001c0001t0002g0103 a0001c0001t0002g0121 a0001c0001t0002g0122 |
3 | NA18962.hp1 NA19066.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.363+3920A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108459850 | |||||||
| chr8:108459852 | CTG | C | 39 | a0001c0001t0003g0002 a0001c0001t0003g0006 a0001c0001t0003g0012 others(36): Show |
56 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(53): Show |
intron_variant | MODIFIER | c.363+3924_363+3925d others(4): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 108459852 | ||||||
| chr8:108459893 | A | T | 161 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(158): Show |
228 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.363+3963A>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108459893 | |||||||
| chr8:108459956 | A | T | 1 | a0001c0001t0003g0083 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.363+4026A>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108459956 | |||||||
| chr8:108460181 | G | T | 161 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(158): Show |
228 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.363+4251G>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108460181 | |||||||
| chr8:108460280 | A | T | 6 | a0001c0001t0002g0007 a0001c0001t0002g0105 a0001c0001t0002g0120 others(3): Show |
9 | HG01934.hp1 HG02056.hp1 HG02074.hp1 others(6): Show |
intron_variant | MODIFIER | c.363+4350A>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108460280 | |||||||
| chr8:108460389 | T | C | 1 | a0001c0001t0022g0052 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.363+4459T>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108460389 | |||||||
| chr8:108460415 | T | C | 1 | a0001c0001t0002g0134 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.363+4485T>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108460415 | |||||||
| chr8:108460531 | C | T | 1 | a0001c0001t0001g0179 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.363+4601C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108460531 | |||||||
| chr8:108460560 | C | T | 1 | a0001c0001t0004g0155 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.363+4630C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108460560 | |||||||
| chr8:108460665 | A | G | 48 | a0001c0001t0004g0015 a0001c0001t0004g0029 a0001c0001t0004g0030 others(45): Show |
61 | HG00733.hp2 HG00738.hp1 HG01074.hp2 others(58): Show |
intron_variant | MODIFIER | c.363+4735A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108460665 | |||||||
| chr8:108460696 | T | C | 2 | a0001c0001t0009g0011 a0001c0001t0009g0060 |
4 | HG02965.hp2 HG03540.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.363+4766T>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108460696 | |||||||
| chr8:108460814 | G | A | 1 | a0001c0001t0003g0073 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.363+4884G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108460814 | |||||||
| chr8:108460927 | T | C | 1 | a0001c0001t0004g0158 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.363+4997T>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108460927 | |||||||
| chr8:108461104 | G | A | 3 | a0001c0001t0008g0217 a0001c0001t0008g0218 a0001c0001t0008g0219 |
3 | HG02922.hp1 HG02965.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.363+5174G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108461104 | |||||||
| chr8:108461163 | T | C | 2 | a0001c0001t0018g0062 a0002c0003t0018g0063 |
2 | HG01109.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.363+5233T>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108461163 | |||||||
| chr8:108461182 | T | G | 2 | a0001c0001t0018g0062 a0002c0003t0018g0063 |
2 | HG01109.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.363+5252T>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108461182 | |||||||
| chr8:108461203 | A | G | 1 | a0001c0001t0026g0082 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.363+5273A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108461203 | |||||||
| chr8:108461319 | A | G | 1 | a0001c0001t0004g0171 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.363+5389A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108461319 | |||||||
| chr8:108461420 | A | G | 1 | a0001c0001t0004g0059 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.363+5490A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108461420 | |||||||
| chr8:108461714 | C | G | 2 | a0001c0001t0003g0087 a0001c0001t0003g0088 |
2 | HG02055.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.363+5784C>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108461714 | |||||||
| chr8:108461797 | C | T | 113 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(110): Show |
167 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.363+5867C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108461797 | |||||||
| chr8:108461819 | T | C | 161 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(158): Show |
228 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.363+5889T>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108461819 | |||||||
| chr8:108461901 | C | T | 1 | a0001c0001t0004g0145 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.363+5971C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108461901 | |||||||
| chr8:108461933 | C | G | 63 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(60): Show |
95 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.363+6003C>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108461933 | |||||||
| chr8:108461936 | G | T | 1 | a0001c0001t0002g0110 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.363+6006G>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108461936 | |||||||
| chr8:108461969 | C | T | 1 | a0001c0002t0003g0091 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.363+6039C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108461969 | |||||||
| chr8:108461974 | A | G | 1 | a0001c0001t0002g0119 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.363+6044A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108461974 | |||||||
| chr8:108462082 | T | C | 165 | a0001c0001t0001g0046 a0001c0001t0001g0233 a0001c0001t0001g0234 others(162): Show |
233 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.363+6152T>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108462082 | |||||||
| chr8:108462121 | A | C | 1 | a0001c0001t0002g0118 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.363+6191A>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108462121 | |||||||
| chr8:108462177 | CGT | C | 2 | a0001c0001t0009g0011 a0001c0001t0015g0045 |
5 | HG02896.hp1 HG02965.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.363+6260_363+6261d others(4): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 108462177 | ||||||
| chr8:108462213 | T | TTGTGTGC others(13): Show |
1 | a0001c0001t0009g0011 | 3 | HG02965.hp2 HG03540.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.363+6290_363+6291i others(22): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 108462213 | ||||||
| chr8:108462213 | T | TTGTGTGC others(11): Show |
1 | a0001c0001t0009g0060 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.363+6300_363+6301i others(20): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 108462213 | ||||||
| chr8:108462213 | T | TTGTGTGC others(13): Show |
94 | a0001c0001t0003g0002 a0001c0001t0003g0006 a0001c0001t0003g0012 others(91): Show |
126 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(123): Show |
intron_variant | MODIFIER | c.363+6300_363+6301i others(22): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 108462213 | ||||||
| chr8:108462213 | T | TTGTGTGC others(15): Show |
2 | a0001c0001t0012g0019 a0001c0001t0012g0061 |
3 | HG03491.hp2 HG03492.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.363+6300_363+6301i others(24): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 108462213 | ||||||
| chr8:108462222 | T | TGTGTGTG others(11): Show |
1 | a0001c0001t0002g0111 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.363+6300_363+6301i others(20): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 108462222 | ||||||
| chr8:108462222 | T | TGTGTGTG others(13): Show |
1 | a0001c0001t0002g0106 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.363+6300_363+6301i others(22): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 108462222 | ||||||
| chr8:108462222 | T | TGTGTGTG others(13): Show |
61 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(58): Show |
93 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(90): Show |
intron_variant | MODIFIER | c.363+6300_363+6301i others(22): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 108462222 | ||||||
| chr8:108462299 | G | T | 1 | a0001c0001t0024g0067 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.363+6369G>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108462299 | |||||||
| chr8:108462308 | A | G | 48 | a0001c0001t0004g0015 a0001c0001t0004g0029 a0001c0001t0004g0030 others(45): Show |
61 | HG00733.hp2 HG00738.hp1 HG01074.hp2 others(58): Show |
intron_variant | MODIFIER | c.363+6378A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108462308 | |||||||
| chr8:108462355 | G | A | 1 | a0001c0001t0028g0236 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.363+6425G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108462355 | |||||||
| chr8:108462470 | G | A | 1 | a0001c0001t0025g0203 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.363+6540G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108462470 | |||||||
| chr8:108462476 | G | T | 1 | a0001c0001t0001g0202 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.363+6546G>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108462476 | |||||||
| chr8:108462548 | C | A | 1 | a0001c0001t0001g0181 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.363+6618C>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108462548 | |||||||
| chr8:108462742 | GT | G | 13 | a0001c0001t0001g0046 a0001c0001t0001g0233 a0001c0001t0001g0234 others(10): Show |
16 | HG00733.hp2 HG02109.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.363+6824delT | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 108462742 | ||||||
| chr8:108462742 | GTT | G | 152 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(149): Show |
217 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.363+6823_363+6824d others(4): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 108462742 | ||||||
| chr8:108462776 | T | C | 1 | a0001c0001t0001g0184 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.363+6846T>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108462776 | |||||||
| chr8:108462976 | A | T | 161 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(158): Show |
228 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.364-6850A>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108462976 | |||||||
| chr8:108463026 | C | T | 1 | a0001c0001t0025g0203 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.364-6800C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108463026 | |||||||
| chr8:108463240 | A | G | 1 | a0001c0001t0016g0055 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.364-6586A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108463240 | |||||||
| chr8:108463287 | G | A | 6 | a0001c0001t0004g0054 a0001c0001t0004g0057 a0001c0001t0004g0058 others(3): Show |
6 | HG00733.hp2 HG02486.hp2 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.364-6539G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108463287 | |||||||
| chr8:108463320 | G | A | 3 | a0001c0001t0007g0020 a0001c0001t0007g0021 a0001c0001t0007g0100 |
5 | HG02257.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.364-6506G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108463320 | |||||||
| chr8:108463372 | A | T | 161 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(158): Show |
228 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.364-6454A>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108463372 | |||||||
| chr8:108463409 | T | A | 2 | a0001c0001t0003g0074 a0001c0001t0026g0082 |
2 | HG01099.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.364-6417T>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108463409 | |||||||
| chr8:108463423 | A | T | 3 | a0001c0001t0007g0020 a0001c0001t0007g0021 a0001c0001t0007g0100 |
5 | HG02257.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.364-6403A>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108463423 | |||||||
| chr8:108463459 | A | G | 1 | a0001c0001t0002g0119 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.364-6367A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108463459 | |||||||
| chr8:108463596 | T | A | 2 | a0001c0001t0001g0035 a0001c0001t0001g0036 |
4 | HG01123.hp1 HG02738.hp1 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.364-6230T>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108463596 | |||||||
| chr8:108463596 | T | G | 1 | a0001c0001t0003g0064 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.364-6230T>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108463596 | |||||||
| chr8:108463914 | T | A | 2 | a0001c0001t0009g0011 a0001c0001t0009g0060 |
4 | HG02965.hp2 HG03540.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.364-5912T>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108463914 | |||||||
| chr8:108463946 | C | T | 2 | a0001c0001t0010g0200 a0001c0001t0010g0201 |
2 | HG00735.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.364-5880C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108463946 | |||||||
| chr8:108464253 | T | A | 2 | a0001c0001t0009g0011 a0001c0001t0009g0060 |
4 | HG02965.hp2 HG03540.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.364-5573T>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108464253 | |||||||
| chr8:108464338 | G | A | 41 | a0001c0001t0004g0015 a0001c0001t0004g0029 a0001c0001t0004g0030 others(38): Show |
53 | HG00738.hp1 HG01074.hp2 HG01167.hp2 others(50): Show |
intron_variant | MODIFIER | c.364-5488G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108464338 | |||||||
| chr8:108464504 | C | G | 1 | a0001c0001t0004g0148 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.364-5322C>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108464504 | |||||||
| chr8:108464598 | C | T | 1 | a0001c0001t0009g0011 | 3 | HG02965.hp2 HG03540.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.364-5228C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108464598 | |||||||
| chr8:108464628 | A | G | 2 | a0001c0001t0012g0019 a0001c0001t0012g0061 |
3 | HG03491.hp2 HG03492.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.364-5198A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108464628 | |||||||
| chr8:108464699 | G | C | 49 | a0001c0001t0003g0002 a0001c0001t0003g0006 a0001c0001t0003g0012 others(46): Show |
71 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(68): Show |
intron_variant | MODIFIER | c.364-5127G>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108464699 | |||||||
| chr8:108464808 | C | T | 1 | a0001c0001t0001g0199 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.364-5018C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108464808 | |||||||
| chr8:108465021 | C | T | 1 | a0001c0001t0022g0052 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.364-4805C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108465021 | |||||||
| chr8:108465204 | G | A | 161 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(158): Show |
228 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.364-4622G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108465204 | |||||||
| chr8:108465220 | G | A | 236 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(233): Show |
348 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(345): Show |
intron_variant | MODIFIER | c.364-4606G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108465220 | |||||||
| chr8:108465294 | A | G | 1 | a0001c0001t0022g0052 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.364-4532A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108465294 | |||||||
| chr8:108465574 | T | G | 1 | a0001c0001t0003g0028 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.364-4252T>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108465574 | |||||||
| chr8:108465614 | A | G | 3 | a0001c0001t0002g0107 a0001c0001t0002g0108 a0001c0001t0002g0244 |
3 | HG01192.hp2 HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.364-4212A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108465614 | |||||||
| chr8:108465638 | A | G | 2 | a0001c0001t0001g0239 a0001c0001t0001g0242 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.364-4188A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108465638 | |||||||
| chr8:108465685 | T | C | 1 | a0001c0001t0003g0075 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.364-4141T>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108465685 | |||||||
| chr8:108465804 | G | A | 161 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(158): Show |
228 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.364-4022G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108465804 | |||||||
| chr8:108465826 | A | G | 2 | a0001c0001t0003g0081 a0001c0001t0003g0099 |
2 | HG03710.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.364-4000A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108465826 | |||||||
| chr8:108465828 | CATTT | C | 6 | a0001c0001t0005g0034 a0001c0001t0005g0150 a0001c0001t0005g0151 others(3): Show |
7 | HG01243.hp2 HG02055.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.364-3996_364-3993d others(6): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 108465828 | ||||||
| chr8:108466029 | A | G | 161 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(158): Show |
228 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.364-3797A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108466029 | |||||||
| chr8:108466051 | T | C | 1 | a0001c0001t0009g0060 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.364-3775T>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108466051 | |||||||
| chr8:108466125 | T | G | 161 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(158): Show |
228 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.364-3701T>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108466125 | |||||||
| chr8:108466176 | G | A | 1 | a0001c0001t0003g0068 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.364-3650G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108466176 | |||||||
| chr8:108466268 | G | A | 246 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(243): Show |
361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
intron_variant | MODIFIER | c.364-3558G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108466268 | |||||||
| chr8:108466307 | T | C | 161 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(158): Show |
228 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.364-3519T>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108466307 | |||||||
| chr8:108466369 | CTTG | C | 5 | a0001c0001t0002g0024 a0001c0001t0002g0107 a0001c0001t0002g0108 others(2): Show |
6 | HG01192.hp2 HG01515.hp2 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.364-3454_364-3452d others(5): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 108466369 | ||||||
| chr8:108466442 | A | AT | 17 | a0001c0001t0001g0009 a0001c0001t0001g0036 a0001c0001t0001g0042 others(14): Show |
22 | HG01099.hp2 HG01361.hp1 HG01433.hp1 others(19): Show |
intron_variant | MODIFIER | c.364-3356dupT | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 108466442 | ||||||
| chr8:108466442 | A | ATTATTTT others(3): Show |
1 | a0001c0001t0025g0203 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.364-3382_364-3381i others(12): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 108466442 | ||||||
| chr8:108466442 | A | ATTTTTTT others(3): Show |
3 | a0001c0001t0008g0217 a0001c0001t0008g0220 a0001c0001t0027g0216 |
3 | HG01261.hp2 HG02717.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.364-3365_364-3356d others(12): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 108466442 | ||||||
| chr8:108466442 | A | ATTTTTTT others(4): Show |
1 | a0001c0001t0008g0219 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.364-3366_364-3356d others(13): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 108466442 | ||||||
| chr8:108466442 | AT | A | 10 | a0001c0001t0001g0017 a0001c0001t0001g0046 a0001c0001t0001g0144 others(7): Show |
13 | HG00558.hp2 HG01256.hp2 HG01257.hp2 others(10): Show |
intron_variant | MODIFIER | c.364-3356delT | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 108466442 | ||||||
| chr8:108466442 | ATTT | A | 9 | a0001c0001t0003g0006 a0001c0001t0003g0064 a0001c0001t0003g0068 others(6): Show |
12 | HG00733.hp1 HG01109.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.364-3358_364-3356d others(5): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 108466442 | ||||||
| chr8:108466442 | ATTTT | A | 36 | a0001c0001t0002g0116 a0001c0001t0002g0120 a0001c0001t0003g0002 others(33): Show |
53 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(50): Show |
intron_variant | MODIFIER | c.364-3359_364-3356d others(6): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 108466442 | ||||||
| chr8:108466442 | ATTTTT | A | 74 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(71): Show |
112 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(109): Show |
intron_variant | MODIFIER | c.364-3360_364-3356d others(7): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 108466442 | ||||||
| chr8:108466442 | ATTTTTT | A | 38 | a0001c0001t0002g0112 a0001c0001t0002g0131 a0001c0001t0002g0132 others(35): Show |
45 | HG00733.hp2 HG00738.hp1 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.364-3361_364-3356d others(8): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 108466442 | ||||||
| chr8:108466442 | ATTTTTTT others(5): Show |
A | 2 | a0001c0001t0016g0055 a0001c0001t0016g0056 |
2 | HG02486.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.364-3367_364-3356d others(14): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 108466442 | ||||||
| chr8:108466518 | T | TTA | 4 | a0001c0001t0006g0016 a0001c0001t0006g0161 a0001c0001t0006g0165 others(1): Show |
6 | HG01255.hp2 HG02004.hp1 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.364-3305_364-3304d others(4): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 108466518 | ||||||
| chr8:108466852 | A | G | 1 | a0001c0001t0014g0169 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.364-2974A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108466852 | |||||||
| chr8:108466993 | A | G | 1 | a0001c0001t0024g0067 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.364-2833A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108466993 | |||||||
| chr8:108467019 | T | G | 2 | a0001c0001t0004g0160 a0001c0001t0004g0163 |
2 | HG02258.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.364-2807T>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108467019 | |||||||
| chr8:108467024 | A | G | 161 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(158): Show |
228 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.364-2802A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108467024 | |||||||
| chr8:108467171 | A | G | 1 | a0001c0001t0031g0117 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.364-2655A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108467171 | |||||||
| chr8:108467216 | C | T | 5 | a0001c0001t0001g0046 a0001c0001t0001g0233 a0001c0001t0001g0234 others(2): Show |
7 | HG02109.hp1 HG02145.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.364-2610C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108467216 | |||||||
| chr8:108467217 | G | A | 1 | a0001c0001t0002g0124 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.364-2609G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108467217 | |||||||
| chr8:108467255 | T | G | 6 | a0001c0001t0004g0054 a0001c0001t0004g0057 a0001c0001t0004g0058 others(3): Show |
6 | HG00733.hp2 HG02486.hp2 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.364-2571T>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108467255 | |||||||
| chr8:108467477 | T | G | 1 | a0001c0001t0024g0067 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.364-2349T>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108467477 | |||||||
| chr8:108467507 | CTCAGCTA others(6): Show |
C | 113 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(110): Show |
167 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.364-2317_364-2305d others(15): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 108467507 | ||||||
| chr8:108467570 | C | T | 161 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(158): Show |
228 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.364-2256C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108467570 | |||||||
| chr8:108467759 | T | G | 1 | a0001c0001t0001g0202 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.364-2067T>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108467759 | |||||||
| chr8:108468055 | A | G | 4 | a0001c0001t0004g0054 a0001c0001t0004g0057 a0001c0001t0004g0058 others(1): Show |
4 | HG00733.hp2 HG02683.hp2 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.364-1771A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108468055 | |||||||
| chr8:108468074 | T | C | 49 | a0001c0001t0003g0002 a0001c0001t0003g0006 a0001c0001t0003g0012 others(46): Show |
71 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(68): Show |
intron_variant | MODIFIER | c.364-1752T>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108468074 | |||||||
| chr8:108468202 | G | A | 1 | a0001c0001t0002g0110 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.364-1624G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108468202 | |||||||
| chr8:108468223 | T | C | 113 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(110): Show |
167 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.364-1603T>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108468223 | |||||||
| chr8:108468248 | T | G | 1 | a0001c0001t0001g0174 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.364-1578T>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108468248 | |||||||
| chr8:108468382 | C | G | 2 | a0001c0001t0001g0039 a0001c0001t0001g0051 |
3 | HG02040.hp1 NA18962.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.364-1444C>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108468382 | |||||||
| chr8:108468494 | A | G | 2 | a0001c0001t0001g0038 a0001c0001t0001g0195 |
3 | NA18960.hp2 NA19070.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.364-1332A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108468494 | |||||||
| chr8:108468541 | A | G | 41 | a0001c0001t0004g0015 a0001c0001t0004g0029 a0001c0001t0004g0030 others(38): Show |
53 | HG00738.hp1 HG01074.hp2 HG01167.hp2 others(50): Show |
intron_variant | MODIFIER | c.364-1285A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108468541 | |||||||
| chr8:108468549 | G | A | 12 | a0001c0001t0002g0005 a0001c0001t0002g0025 a0001c0001t0002g0026 others(9): Show |
18 | HG00438.hp2 NA18612.hp2 NA18943.hp1 others(15): Show |
intron_variant | MODIFIER | c.364-1277G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108468549 | |||||||
| chr8:108468589 | CTTTCA | C | 6 | a0001c0001t0004g0054 a0001c0001t0004g0057 a0001c0001t0004g0058 others(3): Show |
6 | HG00733.hp2 HG02486.hp2 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.364-1232_364-1228d others(7): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 108468589 | ||||||
| chr8:108468809 | G | C | 1 | a0001c0001t0004g0015 | 3 | HG01884.hp1 HG01891.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.364-1017G>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108468809 | |||||||
| chr8:108468858 | C | T | 24 | a0001c0001t0004g0015 a0001c0001t0004g0029 a0001c0001t0004g0030 others(21): Show |
28 | HG01167.hp2 HG01243.hp1 HG01261.hp1 others(25): Show |
intron_variant | MODIFIER | c.364-968C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108468858 | |||||||
| chr8:108468897 | T | G | 1 | a0001c0001t0001g0047 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.364-929T>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108468897 | |||||||
| chr8:108468931 | T | C | 2 | a0001c0001t0005g0050 a0001c0001t0005g0246 |
3 | HG02451.hp1 HG02647.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.364-895T>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108468931 | |||||||
| chr8:108468965 | G | A | 3 | a0001c0002t0003g0089 a0001c0002t0003g0091 a0001c0002t0003g0092 |
3 | HG02970.hp2 HG03041.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.364-861G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108468965 | |||||||
| chr8:108468983 | T | A | 1 | a0001c0001t0001g0207 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.364-843T>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108468983 | |||||||
| chr8:108468994 | G | A | 1 | a0001c0001t0002g0228 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.364-832G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108468994 | |||||||
| chr8:108469007 | G | A | 62 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(59): Show |
94 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(91): Show |
intron_variant | MODIFIER | c.364-819G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108469007 | |||||||
| chr8:108469704 | G | A | 1 | a0001c0001t0001g0196 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.364-122G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 5/10 | chr8 | 108469704 | |||||||
| chr8:108470298 | A | G | 1 | a0001c0001t0024g0067 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.509+177A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 7/10 | chr8 | 108470298 | |||||||
| chr8:108470445 | A | G | 113 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(110): Show |
167 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.509+324A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 7/10 | chr8 | 108470445 | |||||||
| chr8:108470477 | T | C | 2 | a0001c0001t0005g0050 a0001c0001t0005g0246 |
3 | HG02451.hp1 HG02647.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.509+356T>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 7/10 | chr8 | 108470477 | |||||||
| chr8:108470608 | A | G | 2 | a0001c0001t0012g0019 a0001c0001t0012g0061 |
3 | HG03491.hp2 HG03492.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.509+487A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 7/10 | chr8 | 108470608 | |||||||
| chr8:108470808 | T | G | 20 | a0001c0001t0004g0029 a0001c0001t0004g0030 a0001c0001t0004g0031 others(17): Show |
22 | HG01243.hp1 HG01261.hp1 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.509+687T>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 7/10 | chr8 | 108470808 | |||||||
| chr8:108470936 | A | G | 1 | a0001c0001t0004g0145 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.509+815A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 7/10 | chr8 | 108470936 | |||||||
| chr8:108471096 | A | G | 2 | a0001c0001t0018g0062 a0002c0003t0018g0063 |
2 | HG01109.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.509+975A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 7/10 | chr8 | 108471096 | |||||||
| chr8:108471107 | A | G | 161 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(158): Show |
228 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.509+986A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 7/10 | chr8 | 108471107 | |||||||
| chr8:108471299 | A | G | 1 | a0001c0001t0004g0171 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.509+1178A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 7/10 | chr8 | 108471299 | |||||||
| chr8:108471400 | A | G | 1 | a0001c0001t0005g0172 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.509+1279A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 7/10 | chr8 | 108471400 | |||||||
| chr8:108471480 | A | C | 1 | a0001c0001t0001g0194 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.509+1359A>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 7/10 | chr8 | 108471480 | |||||||
| chr8:108471544 | T | C | 2 | a0001c0001t0001g0037 a0001c0001t0001g0185 |
3 | HG00140.hp1 HG00323.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.509+1423T>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 7/10 | chr8 | 108471544 | |||||||
| chr8:108471704 | G | C | 161 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(158): Show |
228 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.509+1583G>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 7/10 | chr8 | 108471704 | |||||||
| chr8:108471855 | C | G | 2 | a0001c0001t0005g0050 a0001c0001t0005g0246 |
3 | HG02451.hp1 HG02647.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.509+1734C>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 7/10 | chr8 | 108471855 | |||||||
| chr8:108471883 | A | G | 1 | a0001c0001t0001g0193 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.509+1762A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 7/10 | chr8 | 108471883 | |||||||
| chr8:108472005 | C | T | 1 | a0001c0001t0028g0236 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.509+1884C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 7/10 | chr8 | 108472005 | |||||||
| chr8:108472290 | T | A | 2 | a0001c0001t0005g0050 a0001c0001t0005g0246 |
3 | HG02451.hp1 HG02647.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.509+2169T>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 7/10 | chr8 | 108472290 | |||||||
| chr8:108472338 | T | C | 1 | a0001c0001t0002g0022 | 2 | HG02683.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.509+2217T>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 7/10 | chr8 | 108472338 | |||||||
| chr8:108472514 | A | G | 49 | a0001c0001t0003g0002 a0001c0001t0003g0006 a0001c0001t0003g0012 others(46): Show |
71 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(68): Show |
intron_variant | MODIFIER | c.509+2393A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 7/10 | chr8 | 108472514 | |||||||
| chr8:108472743 | G | C | 161 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(158): Show |
228 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.509+2622G>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 7/10 | chr8 | 108472743 | |||||||
| chr8:108472761 | C | T | 1 | a0001c0001t0002g0134 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.509+2640C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 7/10 | chr8 | 108472761 | |||||||
| chr8:108472772 | C | T | 1 | a0001c0001t0003g0086 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.509+2651C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 7/10 | chr8 | 108472772 | |||||||
| chr8:108472773 | G | A | 1 | a0001c0001t0015g0045 | 2 | HG02896.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.509+2652G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 7/10 | chr8 | 108472773 | |||||||
| chr8:108472773 | G | C | 4 | a0001c0001t0001g0046 a0001c0001t0001g0233 a0001c0001t0001g0234 others(1): Show |
5 | HG02109.hp1 HG02145.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.509+2652G>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 7/10 | chr8 | 108472773 | |||||||
| chr8:108473056 | A | T | 2 | a0001c0001t0002g0132 a0001c0001t0002g0134 |
2 | HG01433.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.510-2826A>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 7/10 | chr8 | 108473056 | |||||||
| chr8:108473138 | T | C | 2 | a0001c0001t0001g0239 a0001c0001t0001g0242 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.510-2744T>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 7/10 | chr8 | 108473138 | |||||||
| chr8:108473263 | G | A | 161 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(158): Show |
228 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.510-2619G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 7/10 | chr8 | 108473263 | |||||||
| chr8:108473272 | A | G | 62 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(59): Show |
94 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(91): Show |
intron_variant | MODIFIER | c.510-2610A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 7/10 | chr8 | 108473272 | |||||||
| chr8:108473302 | T | C | 2 | a0001c0001t0001g0239 a0001c0001t0001g0242 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.510-2580T>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 7/10 | chr8 | 108473302 | |||||||
| chr8:108473672 | C | CA | 161 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(158): Show |
228 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.510-2208dupA | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr8 | 108473672 | ||||||
| chr8:108473675 | C | G | 161 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(158): Show |
228 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.510-2207C>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 7/10 | chr8 | 108473675 | |||||||
| chr8:108473710 | T | G | 1 | a0001c0001t0015g0045 | 2 | HG02896.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.510-2172T>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 7/10 | chr8 | 108473710 | |||||||
| chr8:108473717 | A | G | 161 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(158): Show |
228 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.510-2165A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 7/10 | chr8 | 108473717 | |||||||
| chr8:108473765 | T | C | 1 | a0001c0001t0001g0207 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.510-2117T>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 7/10 | chr8 | 108473765 | |||||||
| chr8:108473832 | A | G | 1 | a0001c0001t0006g0165 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.510-2050A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 7/10 | chr8 | 108473832 | |||||||
| chr8:108474292 | G | T | 47 | a0001c0001t0004g0015 a0001c0001t0004g0029 a0001c0001t0004g0030 others(44): Show |
60 | HG00733.hp2 HG00738.hp1 HG01074.hp2 others(57): Show |
intron_variant | MODIFIER | c.510-1590G>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 7/10 | chr8 | 108474292 | |||||||
| chr8:108474388 | G | A | 60 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0017 others(57): Show |
101 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.510-1494G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 7/10 | chr8 | 108474388 | |||||||
| chr8:108474447 | A | C | 2 | a0001c0001t0012g0019 a0001c0001t0012g0061 |
3 | HG03491.hp2 HG03492.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.510-1435A>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 7/10 | chr8 | 108474447 | |||||||
| chr8:108474479 | T | C | 1 | a0001c0001t0003g0087 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.510-1403T>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 7/10 | chr8 | 108474479 | |||||||
| chr8:108474554 | TAC | T | 73 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(70): Show |
120 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.510-1306_510-1305d others(4): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr8 | 108474554 | ||||||
| chr8:108474554 | TACAC | T | 162 | a0001c0001t0001g0046 a0001c0001t0001g0233 a0001c0001t0001g0234 others(159): Show |
227 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.510-1308_510-1305d others(6): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr8 | 108474554 | ||||||
| chr8:108474584 | T | C | 1 | a0001c0001t0003g0093 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.510-1298T>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 7/10 | chr8 | 108474584 | |||||||
| chr8:108474782 | T | C | 2 | a0001c0001t0018g0062 a0002c0003t0018g0063 |
2 | HG01109.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.510-1100T>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 7/10 | chr8 | 108474782 | |||||||
| chr8:108474846 | A | G | 1 | a0001c0001t0006g0165 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.510-1036A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 7/10 | chr8 | 108474846 | |||||||
| chr8:108474892 | TACATGTA others(2): Show |
T | 40 | a0001c0001t0003g0002 a0001c0001t0003g0006 a0001c0001t0003g0012 others(37): Show |
57 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(54): Show |
intron_variant | MODIFIER | c.510-985_510-977del others(9): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr8 | 108474892 | ||||||
| chr8:108474948 | A | G | 4 | a0001c0001t0001g0046 a0001c0001t0001g0233 a0001c0001t0001g0234 others(1): Show |
5 | HG02109.hp1 HG02145.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.510-934A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 7/10 | chr8 | 108474948 | |||||||
| chr8:108475234 | G | A | 3 | a0001c0001t0007g0020 a0001c0001t0007g0021 a0001c0001t0007g0100 |
5 | HG02257.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.510-648G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 7/10 | chr8 | 108475234 | |||||||
| chr8:108475236 | C | T | 32 | a0001c0001t0004g0015 a0001c0001t0004g0029 a0001c0001t0004g0030 others(29): Show |
40 | HG00738.hp1 HG01074.hp2 HG01167.hp2 others(37): Show |
intron_variant | MODIFIER | c.510-646C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 7/10 | chr8 | 108475236 | |||||||
| chr8:108475487 | C | T | 1 | a0001c0001t0003g0094 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.510-395C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 7/10 | chr8 | 108475487 | |||||||
| chr8:108475737 | A | G | 62 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(59): Show |
94 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(91): Show |
intron_variant | MODIFIER | c.510-145A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 7/10 | chr8 | 108475737 | |||||||
| chr8:108476208 | T | C | 1 | a0001c0001t0002g0125 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.591+245T>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 8/10 | chr8 | 108476208 | |||||||
| chr8:108476309 | A | G | 6 | a0001c0001t0005g0034 a0001c0001t0005g0150 a0001c0001t0005g0151 others(3): Show |
7 | HG01243.hp2 HG02055.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.591+346A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 8/10 | chr8 | 108476309 | |||||||
| chr8:108476321 | G | A | 1 | a0001c0001t0004g0148 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.591+358G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 8/10 | chr8 | 108476321 | |||||||
| chr8:108476358 | A | G | 1 | a0001c0001t0022g0052 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.591+395A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 8/10 | chr8 | 108476358 | |||||||
| chr8:108476361 | A | G | 62 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(59): Show |
94 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(91): Show |
intron_variant | MODIFIER | c.591+398A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 8/10 | chr8 | 108476361 | |||||||
| chr8:108476418 | A | C | 6 | a0001c0001t0004g0054 a0001c0001t0004g0057 a0001c0001t0004g0058 others(3): Show |
6 | HG00733.hp2 HG02486.hp2 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.592-364A>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 8/10 | chr8 | 108476418 | |||||||
| chr8:108476436 | T | G | 1 | a0001c0001t0002g0124 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.592-346T>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 8/10 | chr8 | 108476436 | |||||||
| chr8:108476450 | A | G | 1 | a0001c0001t0002g0108 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.592-332A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 8/10 | chr8 | 108476450 | |||||||
| chr8:108476625 | T | C | 1 | a0001c0001t0008g0218 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.592-157T>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 8/10 | chr8 | 108476625 | |||||||
| chr8:108476708 | A | G | 162 | a0001c0001t0001g0144 a0001c0001t0002g0003 a0001c0001t0002g0004 others(159): Show |
229 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.592-74A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 8/10 | chr8 | 108476708 | |||||||
| chr8:108477007 | T | C | 1 | a0001c0001t0015g0045 | 2 | HG02896.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.702+115T>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 9/10 | chr8 | 108477007 | |||||||
| chr8:108477041 | G | A | 161 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(158): Show |
228 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.702+149G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 9/10 | chr8 | 108477041 | |||||||
| chr8:108477162 | G | A | 161 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(158): Show |
228 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.702+270G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 9/10 | chr8 | 108477162 | |||||||
| chr8:108477281 | C | A | 55 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(52): Show |
84 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.702+389C>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 9/10 | chr8 | 108477281 | |||||||
| chr8:108477290 | A | G | 1 | a0001c0001t0022g0052 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.702+398A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 9/10 | chr8 | 108477290 | |||||||
| chr8:108477470 | C | T | 1 | a0001c0001t0002g0115 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.702+578C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 9/10 | chr8 | 108477470 | |||||||
| chr8:108477745 | G | A | 1 | a0001c0001t0015g0045 | 2 | HG02896.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.702+853G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 9/10 | chr8 | 108477745 | |||||||
| chr8:108477947 | A | G | 41 | a0001c0001t0004g0015 a0001c0001t0004g0029 a0001c0001t0004g0030 others(38): Show |
53 | HG00738.hp1 HG01074.hp2 HG01167.hp2 others(50): Show |
intron_variant | MODIFIER | c.702+1055A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 9/10 | chr8 | 108477947 | |||||||
| chr8:108477950 | A | G | 1 | a0001c0001t0003g0080 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.703-1056A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 9/10 | chr8 | 108477950 | |||||||
| chr8:108478456 | G | A | 2 | a0001c0001t0003g0074 a0001c0001t0026g0082 |
2 | HG01099.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.703-550G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 9/10 | chr8 | 108478456 | |||||||
| chr8:108478513 | T | C | 161 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(158): Show |
228 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.703-493T>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 9/10 | chr8 | 108478513 | |||||||
| chr8:108478702 | G | T | 161 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(158): Show |
228 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.703-304G>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 9/10 | chr8 | 108478702 | |||||||
| chr8:108478737 | T | G | 3 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0186 |
3 | NA18947.hp1 NA18956.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.703-269T>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 9/10 | chr8 | 108478737 | |||||||
| chr8:108478743 | G | C | 1 | a0001c0001t0002g0133 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.703-263G>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 9/10 | chr8 | 108478743 | |||||||
| chr8:108478796 | C | T | 1 | a0001c0001t0022g0052 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.703-210C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 9/10 | chr8 | 108478796 | |||||||
| chr8:108478847 | T | G | 2 | a0001c0001t0005g0050 a0001c0001t0005g0246 |
3 | HG02451.hp1 HG02647.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.703-159T>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 9/10 | chr8 | 108478847 | |||||||
| chr8:108478880 | A | G | 4 | a0001c0001t0001g0046 a0001c0001t0001g0233 a0001c0001t0001g0234 others(1): Show |
5 | HG02109.hp1 HG02145.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.703-126A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 9/10 | chr8 | 108478880 | |||||||
| chr8:108478905 | A | T | 1 | a0001c0001t0001g0195 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.703-101A>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 9/10 | chr8 | 108478905 | |||||||
| chr8:108479170 | A | T | 161 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(158): Show |
228 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.807+60A>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108479170 | |||||||
| chr8:108479320 | T | C | 1 | a0001c0001t0001g0187 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.807+210T>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108479320 | |||||||
| chr8:108479367 | A | G | 1 | a0001c0001t0015g0045 | 2 | HG02896.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.807+257A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108479367 | |||||||
| chr8:108479447 | T | C | 2 | a0001c0001t0001g0239 a0001c0001t0001g0242 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.807+337T>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108479447 | |||||||
| chr8:108479576 | G | A | 40 | a0001c0001t0003g0002 a0001c0001t0003g0006 a0001c0001t0003g0012 others(37): Show |
57 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(54): Show |
intron_variant | MODIFIER | c.807+466G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108479576 | |||||||
| chr8:108479680 | A | G | 1 | a0001c0001t0023g0213 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.807+570A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108479680 | |||||||
| chr8:108479699 | GA | G | 1 | a0001c0001t0004g0015 | 3 | HG01884.hp1 HG01891.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.807+590delA | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108479699 | |||||||
| chr8:108479871 | T | G | 237 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(234): Show |
349 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(346): Show |
intron_variant | MODIFIER | c.807+761T>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108479871 | |||||||
| chr8:108479941 | T | C | 2 | a0001c0001t0014g0169 a0001c0001t0014g0170 |
2 | HG01167.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.807+831T>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108479941 | |||||||
| chr8:108479990 | C | T | 2 | a0001c0001t0002g0026 a0003c0004t0002g0128 |
3 | NA18976.hp2 NA18983.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.807+880C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108479990 | |||||||
| chr8:108480185 | G | A | 1 | a0001c0001t0003g0076 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.807+1075G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108480185 | |||||||
| chr8:108480192 | G | A | 161 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(158): Show |
228 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.807+1082G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108480192 | |||||||
| chr8:108480237 | A | T | 1 | a0001c0001t0022g0052 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.807+1127A>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108480237 | |||||||
| chr8:108480335 | G | A | 1 | a0001c0001t0014g0170 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.807+1225G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108480335 | |||||||
| chr8:108480336 | G | T | 1 | a0001c0001t0014g0170 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.807+1226G>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108480336 | |||||||
| chr8:108480341 | A | G | 165 | a0001c0001t0001g0046 a0001c0001t0001g0233 a0001c0001t0001g0234 others(162): Show |
233 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.807+1231A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108480341 | |||||||
| chr8:108480841 | T | C | 1 | a0001c0001t0002g0129 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.807+1731T>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108480841 | |||||||
| chr8:108481009 | G | C | 1 | a0001c0001t0002g0013 | 3 | NA19001.hp2 NA19005.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.807+1899G>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108481009 | |||||||
| chr8:108481149 | C | T | 161 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(158): Show |
228 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.807+2039C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108481149 | |||||||
| chr8:108481266 | A | G | 2 | a0001c0001t0005g0050 a0001c0001t0005g0246 |
3 | HG02451.hp1 HG02647.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.807+2156A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108481266 | |||||||
| chr8:108481269 | A | G | 1 | a0001c0001t0001g0197 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.807+2159A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108481269 | |||||||
| chr8:108481421 | CAG | C | 2 | a0001c0001t0005g0034 a0001c0001t0005g0172 |
3 | HG01243.hp2 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.807+2314_807+2315d others(4): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr8 | 108481421 | ||||||
| chr8:108481599 | A | G | 2 | a0001c0001t0001g0192 a0001c0001t0001g0194 |
2 | HG00438.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.807+2489A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108481599 | |||||||
| chr8:108481663 | A | C | 48 | a0001c0001t0004g0015 a0001c0001t0004g0029 a0001c0001t0004g0030 others(45): Show |
61 | HG00733.hp2 HG00738.hp1 HG01074.hp2 others(58): Show |
intron_variant | MODIFIER | c.807+2553A>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108481663 | |||||||
| chr8:108481830 | T | C | 63 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(60): Show |
95 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.807+2720T>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108481830 | |||||||
| chr8:108481833 | A | G | 1 | a0001c0001t0002g0141 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.807+2723A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108481833 | |||||||
| chr8:108481905 | T | C | 1 | a0001c0001t0003g0096 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.807+2795T>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108481905 | |||||||
| chr8:108481934 | G | A | 1 | a0001c0001t0001g0051 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.807+2824G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108481934 | |||||||
| chr8:108482273 | G | T | 24 | a0001c0001t0004g0015 a0001c0001t0004g0029 a0001c0001t0004g0030 others(21): Show |
28 | HG01167.hp2 HG01243.hp1 HG01261.hp1 others(25): Show |
intron_variant | MODIFIER | c.807+3163G>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108482273 | |||||||
| chr8:108482360 | G | A | 1 | a0001c0001t0011g0014 | 3 | HG01884.hp2 HG02486.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.807+3250G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108482360 | |||||||
| chr8:108482383 | C | T | 1 | a0001c0001t0001g0191 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.807+3273C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108482383 | |||||||
| chr8:108482426 | G | A | 161 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(158): Show |
228 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.807+3316G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108482426 | |||||||
| chr8:108482609 | CTGGT | C | 161 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(158): Show |
228 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.807+3505_807+3508d others(6): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr8 | 108482609 | ||||||
| chr8:108482728 | C | T | 2 | a0001c0001t0016g0055 a0001c0001t0016g0056 |
2 | HG02486.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.807+3618C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108482728 | |||||||
| chr8:108482738 | C | T | 47 | a0001c0001t0004g0015 a0001c0001t0004g0029 a0001c0001t0004g0030 others(44): Show |
60 | HG00733.hp2 HG00738.hp1 HG01074.hp2 others(57): Show |
intron_variant | MODIFIER | c.807+3628C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108482738 | |||||||
| chr8:108482828 | C | T | 1 | a0001c0001t0001g0207 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.808-3684C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108482828 | |||||||
| chr8:108483204 | C | T | 1 | a0001c0001t0021g0190 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.808-3308C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108483204 | |||||||
| chr8:108483389 | A | G | 41 | a0001c0001t0004g0015 a0001c0001t0004g0029 a0001c0001t0004g0030 others(38): Show |
53 | HG00738.hp1 HG01074.hp2 HG01167.hp2 others(50): Show |
intron_variant | MODIFIER | c.808-3123A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108483389 | |||||||
| chr8:108483421 | T | G | 1 | a0001c0001t0004g0015 | 3 | HG01884.hp1 HG01891.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.808-3091T>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108483421 | |||||||
| chr8:108483650 | A | G | 48 | a0001c0001t0004g0015 a0001c0001t0004g0029 a0001c0001t0004g0030 others(45): Show |
61 | HG00733.hp2 HG00738.hp1 HG01074.hp2 others(58): Show |
intron_variant | MODIFIER | c.808-2862A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108483650 | |||||||
| chr8:108483918 | G | A | 2 | a0001c0001t0003g0028 a0001c0001t0003g0079 |
3 | HG01168.hp2 HG01169.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.808-2594G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108483918 | |||||||
| chr8:108483945 | G | T | 161 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(158): Show |
228 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.808-2567G>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108483945 | |||||||
| chr8:108484051 | G | T | 161 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(158): Show |
228 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.808-2461G>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108484051 | |||||||
| chr8:108484167 | T | C | 1 | a0001c0001t0003g0084 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.808-2345T>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108484167 | |||||||
| chr8:108484261 | A | G | 7 | a0001c0001t0004g0054 a0001c0001t0004g0057 a0001c0001t0004g0058 others(4): Show |
8 | HG00733.hp2 HG02486.hp2 HG02683.hp2 others(5): Show |
intron_variant | MODIFIER | c.808-2251A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108484261 | |||||||
| chr8:108484312 | A | T | 1 | a0001c0001t0001g0207 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.808-2200A>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108484312 | |||||||
| chr8:108484460 | C | G | 1 | a0001c0001t0001g0209 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.808-2052C>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108484460 | |||||||
| chr8:108484463 | T | C | 118 | a0001c0001t0001g0046 a0001c0001t0001g0233 a0001c0001t0001g0234 others(115): Show |
173 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.808-2049T>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108484463 | |||||||
| chr8:108484705 | C | A | 1 | a0001c0001t0001g0188 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.808-1807C>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108484705 | |||||||
| chr8:108485042 | T | A | 1 | a0001c0001t0001g0189 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.808-1470T>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108485042 | |||||||
| chr8:108485048 | A | C | 1 | a0001c0001t0002g0141 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.808-1464A>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108485048 | |||||||
| chr8:108485093 | A | G | 1 | a0001c0001t0002g0027 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.808-1419A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108485093 | |||||||
| chr8:108485117 | G | T | 1 | a0001c0001t0001g0191 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.808-1395G>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108485117 | |||||||
| chr8:108485274 | A | G | 1 | a0001c0001t0002g0114 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.808-1238A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108485274 | |||||||
| chr8:108485321 | T | A | 1 | a0001c0001t0002g0113 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.808-1191T>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108485321 | |||||||
| chr8:108485325 | T | A | 1 | a0001c0001t0002g0113 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.808-1187T>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108485325 | |||||||
| chr8:108485327 | G | A | 1 | a0001c0001t0002g0113 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.808-1185G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108485327 | |||||||
| chr8:108485329 | T | A | 1 | a0001c0001t0002g0113 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.808-1183T>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108485329 | |||||||
| chr8:108485330 | T | G | 1 | a0001c0001t0002g0113 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.808-1182T>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108485330 | |||||||
| chr8:108485331 | G | T | 1 | a0001c0001t0002g0113 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.808-1181G>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108485331 | |||||||
| chr8:108485332 | A | C | 160 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(157): Show |
227 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.808-1180A>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108485332 | |||||||
| chr8:108485334 | G | T | 1 | a0001c0001t0002g0113 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.808-1178G>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108485334 | |||||||
| chr8:108485362 | A | G | 6 | a0001c0001t0004g0054 a0001c0001t0004g0057 a0001c0001t0004g0058 others(3): Show |
6 | HG00733.hp2 HG02486.hp2 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.808-1150A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108485362 | |||||||
| chr8:108485452 | T | TACATATA others(17): Show |
8 | a0001c0001t0006g0016 a0001c0001t0006g0032 a0001c0001t0006g0149 others(5): Show |
12 | HG00738.hp1 HG01074.hp2 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.808-1048_808-1025d others(26): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr8 | 108485452 | ||||||
| chr8:108485533 | A | T | 1 | a0001c0001t0002g0113 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.808-979A>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108485533 | |||||||
| chr8:108485549 | A | G | 1 | a0001c0001t0002g0113 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.808-963A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108485549 | |||||||
| chr8:108485552 | TATAC | T | 4 | a0001c0001t0001g0046 a0001c0001t0001g0233 a0001c0001t0001g0234 others(1): Show |
5 | HG02109.hp1 HG02145.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.808-958_808-955del others(4): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr8 | 108485552 | ||||||
| chr8:108485552 | TATACAC | T | 160 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(157): Show |
227 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.808-958_808-953del others(6): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr8 | 108485552 | ||||||
| chr8:108485556 | C | T | 1 | a0001c0001t0002g0113 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.808-956C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108485556 | |||||||
| chr8:108485558 | C | T | 1 | a0001c0001t0002g0113 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.808-954C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108485558 | |||||||
| chr8:108485703 | G | A | 1 | a0001c0001t0001g0175 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.808-809G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108485703 | |||||||
| chr8:108486060 | T | C | 161 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(158): Show |
228 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.808-452T>C | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108486060 | |||||||
| chr8:108486150 | C | T | 2 | a0001c0001t0018g0062 a0002c0003t0018g0063 |
2 | HG01109.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.808-362C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108486150 | |||||||
| chr8:108486173 | C | T | 1 | a0001c0001t0002g0116 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.808-339C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108486173 | |||||||
| chr8:108486206 | C | CAT | 161 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(158): Show |
228 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.808-305_808-304dup others(2): Show |
EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr8 | 108486206 | ||||||
| chr8:108486291 | G | A | 1 | a0001c0001t0015g0045 | 2 | HG02896.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.808-221G>A | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108486291 | |||||||
| chr8:108486328 | C | T | 6 | a0001c0001t0008g0217 a0001c0001t0008g0218 a0001c0001t0008g0219 others(3): Show |
6 | HG01261.hp2 HG02717.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.808-184C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108486328 | |||||||
| chr8:108486352 | C | G | 1 | a0001c0001t0001g0184 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.808-160C>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108486352 | |||||||
| chr8:108486427 | T | G | 161 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(158): Show |
228 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.808-85T>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108486427 | |||||||
| chr8:108486430 | C | T | 1 | a0001c0001t0011g0014 | 3 | HG01884.hp2 HG02486.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.808-82C>T | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108486430 | |||||||
| chr8:108486452 | A | G | 6 | a0001c0001t0004g0054 a0001c0001t0004g0057 a0001c0001t0004g0058 others(3): Show |
6 | HG00733.hp2 HG02486.hp2 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.808-60A>G | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | chr8 | 108486452 | |||||||
| chr8:108486488 | C | CT | 84 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(81): Show |
132 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(129): Show |
splice_region_variant&intron_variant | LOW | c.808-7dupT | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr8 | 108486488 | ||||||
| chr8:108486488 | C | CTT | 42 | a0001c0001t0002g0121 a0001c0001t0002g0135 a0001c0001t0003g0077 others(39): Show |
53 | HG00733.hp2 HG00738.hp1 HG01070.hp1 others(50): Show |
splice_region_variant&intron_variant | LOW | c.808-8_808-7dupTT | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr8 | 108486488 | ||||||
| chr8:108486488 | C | CTTT | 111 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(108): Show |
166 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(163): Show |
splice_region_variant&intron_variant | LOW | c.808-9_808-7dupTTT | EMC2 | ENSG00000104412.8 | transcript | ENST00000220853.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr8 | 108486488 |