Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 284611 |
| ensemblid | ENSG00000162636.16 |
| hgncid | 27637 |
| symbol | EEIG2 |
| name | EEIG family member 2 |
| refseq_nuc | NM_001010883.3 |
| refseq_prot | NP_001010883.2 |
| ensembl_nuc | ENST00000370035.8 |
| ensembl_prot | ENSP00000359052.3 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 108560100 |
| end | 108639322 |
| strand | + |
| ver | v1.2 |
| region | chr1:108560100-108639322 |
| region5000 | chr1:108555100-108644322 |
| regionname0 | EEIG2_chr1_108560100_108639322 |
| regionname5000 | EEIG2_chr1_108555100_108644322 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1080 | 272 | 76 | 54 | 116 | 0 | 24 | EEIG2_chr1_108555100_108644322 | EEIG2 | ATGAT others(1075): Show |
chr1 | 108555100 | 108644322 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 5586 | 113 | 18 | 29 | 53 | 0 | 12 | EEIG2_chr1_108555100_108644322 | EEIG2 | AGACG others(5581): Show |
chr1 | 108555100 | 108644322 |
| a0001c0001t0002 | 0/0 | 5585 | 62 | 10 | 15 | 32 | 0 | 5 | EEIG2_chr1_108555100_108644322 | EEIG2 | AGACG others(5580): Show |
chr1 | 108555100 | 108644322 |
| a0001c0001t0003 | 0/0 | 5586 | 24 | 0 | 0 | 23 | 0 | 1 | EEIG2_chr1_108555100_108644322 | EEIG2 | AGACG others(5581): Show |
chr1 | 108555100 | 108644322 |
| a0001c0001t0004 | 0/0 | 5597 | 16 | 16 | 0 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | AGACG others(5592): Show |
chr1 | 108555100 | 108644322 |
| a0001c0001t0005 | 0/0 | 5586 | 9 | 0 | 1 | 3 | 0 | 5 | EEIG2_chr1_108555100_108644322 | EEIG2 | AGACG others(5581): Show |
chr1 | 108555100 | 108644322 |
| a0001c0001t0006 | 0/0 | 5586 | 6 | 6 | 0 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | AGACG others(5581): Show |
chr1 | 108555100 | 108644322 |
| a0001c0001t0007 | 0/0 | 5586 | 5 | 5 | 0 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | AGACG others(5581): Show |
chr1 | 108555100 | 108644322 |
| a0001c0001t0008 | 1/0 | 5584 | 5 | 4 | 0 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | AGACG others(5579): Show |
chr1 | 108555100 | 108644322 |
| a0001c0001t0009 | 0/0 | 5559 | 2 | 0 | 2 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | AGACG others(5554): Show |
chr1 | 108555100 | 108644322 |
| a0001c0001t0010 | 0/0 | 5586 | 2 | 0 | 2 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | AGACG others(5581): Show |
chr1 | 108555100 | 108644322 |
| a0001c0001t0011 | 0/0 | 5569 | 2 | 0 | 2 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | AGACG others(5564): Show |
chr1 | 108555100 | 108644322 |
| a0001c0001t0012 | 0/0 | 5586 | 2 | 0 | 0 | 2 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | AGACG others(5581): Show |
chr1 | 108555100 | 108644322 |
| a0001c0001t0013 | 0/0 | 5586 | 2 | 2 | 0 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | AGACG others(5581): Show |
chr1 | 108555100 | 108644322 |
| a0001c0001t0014 | 0/0 | 5585 | 2 | 2 | 0 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | AGACG others(5580): Show |
chr1 | 108555100 | 108644322 |
| a0001c0001t0015 | 0/0 | 5585 | 2 | 2 | 0 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | AGACG others(5580): Show |
chr1 | 108555100 | 108644322 |
| a0001c0001t0016 | 0/0 | 5565 | 2 | 2 | 0 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | AGACG others(5560): Show |
chr1 | 108555100 | 108644322 |
| a0001c0001t0017 | 0/0 | 5586 | 1 | 0 | 0 | 1 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | AGACG others(5581): Show |
chr1 | 108555100 | 108644322 |
| a0001c0001t0018 | 0/0 | 5585 | 1 | 0 | 1 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | AGACG others(5580): Show |
chr1 | 108555100 | 108644322 |
| a0001c0001t0019 | 0/0 | 5585 | 1 | 0 | 0 | 1 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | AGACG others(5580): Show |
chr1 | 108555100 | 108644322 |
| a0001c0001t0020 | 0/0 | 5586 | 1 | 0 | 1 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | AGACG others(5581): Show |
chr1 | 108555100 | 108644322 |
| a0001c0001t0021 | 0/0 | 5586 | 1 | 0 | 0 | 1 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | AGACG others(5581): Show |
chr1 | 108555100 | 108644322 |
| a0001c0001t0022 | 0/0 | 5585 | 1 | 0 | 1 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | AGACG others(5580): Show |
chr1 | 108555100 | 108644322 |
| a0001c0001t0023 | 0/0 | 5586 | 1 | 1 | 0 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | AGACG others(5581): Show |
chr1 | 108555100 | 108644322 |
| a0001c0001t0024 | 0/0 | 5585 | 1 | 1 | 0 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | AGACG others(5580): Show |
chr1 | 108555100 | 108644322 |
| a0001c0001t0025 | 0/0 | 5586 | 1 | 1 | 0 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | AGACG others(5581): Show |
chr1 | 108555100 | 108644322 |
| a0001c0001t0026 | 0/0 | 5585 | 1 | 1 | 0 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | AGACG others(5580): Show |
chr1 | 108555100 | 108644322 |
| a0001c0001t0027 | 0/0 | 5585 | 1 | 1 | 0 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | AGACG others(5580): Show |
chr1 | 108555100 | 108644322 |
| a0001c0001t0028 | 0/0 | 5585 | 1 | 0 | 0 | 0 | 0 | 1 | EEIG2_chr1_108555100_108644322 | EEIG2 | AGACG others(5580): Show |
chr1 | 108555100 | 108644322 |
| a0001c0001t0029 | 0/0 | 5585 | 1 | 1 | 0 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | AGACG others(5580): Show |
chr1 | 108555100 | 108644322 |
| a0001c0001t0030 | 0/0 | 5585 | 1 | 1 | 0 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | AGACG others(5580): Show |
chr1 | 108555100 | 108644322 |
| a0001c0001t0031 | 0/0 | 5585 | 1 | 1 | 0 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | AGACG others(5580): Show |
chr1 | 108555100 | 108644322 |
| a0001c0001t0032 | 0/0 | 5586 | 1 | 1 | 0 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | AGACG others(5581): Show |
chr1 | 108555100 | 108644322 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0001g0017 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0002g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0002g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0002g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0002g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0002g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0002g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0002g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0002g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0002g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0002g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0003g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0003g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0003g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0003g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0003g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0003g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0003g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0003g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0003g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0003g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0003g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0003g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0003g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0003g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0003g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0003g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0003g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0003g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0003g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0003g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0003g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0003g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0004g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0004g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0004g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0004g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0004g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0004g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0004g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0004g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0004g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0004g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0004g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0004g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0004g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0004g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0004g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0004g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0005g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0005g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0005g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0005g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0005g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0005g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0005g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0005g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0005g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0006g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0006g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0006g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0006g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0006g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0006g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0007g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0007g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0007g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0007g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0007g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0008g0004 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0008g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0008g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0008g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0009g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0009g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0010g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0010g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0011g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0011g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0012g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0012g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0013g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0013g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0014g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0014g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0015g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0015g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0016g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0016g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0017g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0018g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0019g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0020g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0021g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0022g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0023g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0024g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0025g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0026g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0027g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0028g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0029g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0030g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0031g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| a0001c0001t0032g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | CHS | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0196 | EAS | CHS | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG00423 | hp1 | a0001 | c0001 | t0003 | g0242 | EAS | CHS | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | CHS | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | PUR | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0095 | AMR | PUR | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG00735 | hp1 | a0001 | c0001 | t0010 | g0120 | AMR | PUR | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG00738 | hp1 | a0001 | c0001 | t0011 | g0027 | AMR | PUR | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0079 | AMR | PUR | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0008 | AMR | PUR | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG01070 | hp2 | a0001 | c0001 | t0018 | g0002 | AMR | PUR | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG01071 | hp1 | a0001 | c0001 | t0010 | g0002 | AMR | PUR | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0008 | AMR | PUR | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0064 | AMR | PUR | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | PUR | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG01243 | hp2 | a0001 | c0001 | t0005 | g0116 | AMR | PUR | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0099 | AMR | CLM | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG01257 | hp1 | a0001 | c0001 | t0009 | g0021 | AMR | CLM | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | CLM | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG01258 | hp1 | a0001 | c0001 | t0009 | g0023 | AMR | CLM | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | CLM | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | CLM | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | CLM | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | CLM | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0203 | AMR | CLM | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0146 | AMR | CLM | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0192 | AMR | CLM | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | ACB | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG01884 | hp2 | a0001 | c0001 | t0014 | g0235 | AFR | ACB | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG01891 | hp1 | a0001 | c0001 | t0004 | g0167 | AFR | ACB | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG01891 | hp2 | a0001 | c0001 | t0008 | g0136 | AFR | ACB | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0220 | AMR | PEL | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0066 | AMR | PEL | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0201 | AMR | PEL | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG01943 | hp1 | a0001 | c0001 | t0020 | g0051 | AMR | PEL | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0224 | AMR | PEL | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0208 | AMR | PEL | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | PEL | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | PEL | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0225 | AMR | PEL | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0097 | AMR | PEL | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG01978 | hp2 | a0001 | c0001 | t0011 | g0028 | AMR | PEL | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | PEL | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG01981 | hp2 | a0001 | c0001 | t0022 | g0013 | AMR | PEL | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0212 | AMR | PEL | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | PEL | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0141 | AMR | PEL | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0226 | AMR | PEL | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG02015 | hp1 | a0001 | c0001 | t0005 | g0115 | EAS | KHV | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG02015 | hp2 | a0001 | c0001 | t0012 | g0090 | EAS | KHV | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG02027 | hp1 | a0001 | c0001 | t0012 | g0057 | EAS | KHV | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0191 | EAS | KHV | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | KHV | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | KHV | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG02055 | hp1 | a0001 | c0001 | t0025 | g0161 | AFR | ACB | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | ACB | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | KHV | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG02135 | hp2 | a0001 | c0001 | t0003 | g0252 | EAS | KHV | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0006 | AFR | ACB | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG02145 | hp2 | a0001 | c0001 | t0004 | g0170 | AFR | ACB | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0068 | AMR | PEL | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0193 | AMR | PEL | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0194 | EAS | CDX | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | CDX | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | CDX | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0197 | EAS | CDX | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG02258 | hp1 | a0001 | c0001 | t0004 | g0166 | AFR | ACB | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG02258 | hp2 | a0001 | c0001 | t0016 | g0160 | AFR | ACB | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG02451 | hp1 | a0001 | c0001 | t0008 | g0134 | AFR | ACB | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG02451 | hp2 | a0001 | c0001 | t0007 | g0029 | AFR | ACB | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG02572 | hp1 | a0001 | c0001 | t0004 | g0152 | AFR | GWD | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | GWD | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0187 | AFR | GWD | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG02630 | hp1 | a0001 | c0001 | t0029 | g0174 | AFR | GWD | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG02630 | hp2 | a0001 | c0001 | t0004 | g0164 | AFR | GWD | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG02647 | hp1 | a0001 | c0001 | t0015 | g0172 | AFR | GWD | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG02647 | hp2 | a0001 | c0001 | t0007 | g0026 | AFR | GWD | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0144 | SAS | PJL | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0184 | SAS | PJL | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0188 | AFR | GWD | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG02717 | hp2 | a0001 | c0001 | t0004 | g0154 | AFR | GWD | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0048 | SAS | PJL | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG02738 | hp2 | a0001 | c0001 | t0005 | g0122 | SAS | PJL | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG02809 | hp1 | a0001 | c0001 | t0004 | g0162 | AFR | GWD | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG02809 | hp2 | a0001 | c0001 | t0004 | g0151 | AFR | GWD | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG02886 | hp1 | a0001 | c0001 | t0027 | g0183 | AFR | GWD | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG02886 | hp2 | a0001 | c0001 | t0006 | g0178 | AFR | GWD | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG02895 | hp1 | a0001 | c0001 | t0006 | g0182 | AFR | GWD | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0007 | AFR | GWD | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG02896 | hp1 | a0001 | c0001 | t0023 | g0132 | AFR | GWD | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | GWD | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | GWD | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG02897 | hp2 | a0001 | c0001 | t0006 | g0181 | AFR | GWD | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG02922 | hp1 | a0001 | c0001 | t0004 | g0149 | AFR | ESN | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0007 | AFR | ESN | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG02965 | hp1 | a0001 | c0001 | t0004 | g0163 | AFR | ESN | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | ESN | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG02970 | hp1 | a0001 | c0001 | t0016 | g0159 | AFR | ESN | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | ESN | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | ESN | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG02976 | hp2 | a0001 | c0001 | t0014 | g0234 | AFR | ESN | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG03041 | hp1 | a0001 | c0001 | t0007 | g0020 | AFR | GWD | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG03041 | hp2 | a0001 | c0001 | t0006 | g0158 | AFR | GWD | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG03130 | hp1 | a0001 | c0001 | t0013 | g0176 | AFR | ESN | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG03130 | hp2 | a0001 | c0001 | t0008 | g0004 | AFR | ESN | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0006 | AFR | ESN | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | ESN | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | MSL | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG03453 | hp2 | a0001 | c0001 | t0015 | g0173 | AFR | MSL | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG03486 | hp1 | a0001 | c0001 | t0006 | g0180 | AFR | MSL | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG03486 | hp2 | a0001 | c0001 | t0007 | g0019 | AFR | MSL | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0211 | SAS | PJL | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0035 | SAS | PJL | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG03492 | hp1 | a0001 | c0001 | t0005 | g0114 | SAS | PJL | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0034 | SAS | PJL | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0177 | AFR | ESN | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG03516 | hp2 | a0001 | c0001 | t0030 | g0175 | AFR | ESN | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG03540 | hp2 | a0001 | c0001 | t0004 | g0169 | AFR | GWD | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | MSL | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG03579 | hp2 | a0001 | c0001 | t0004 | g0150 | AFR | MSL | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0233 | SAS | PJL | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG03669 | hp2 | a0001 | c0001 | t0003 | g0249 | SAS | PJL | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0133 | SAS | PJL | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG03710 | hp2 | a0001 | c0001 | t0005 | g0123 | SAS | PJL | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG03831 | hp1 | a0001 | c0001 | t0005 | g0124 | SAS | BEB | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0210 | SAS | BEB | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0082 | SAS | BEB | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0030 | SAS | BEB | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0055 | SAS | STU | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0236 | SAS | STU | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0036 | SAS | STU | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | STU | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG04228 | hp1 | a0001 | c0001 | t0005 | g0121 | SAS | STU | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0070 | SAS | STU | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| NA18522 | hp1 | a0001 | c0001 | t0032 | g0262 | AFR | YRI | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| NA18522 | hp2 | a0001 | c0001 | t0007 | g0018 | AFR | YRI | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0205 | EAS | CHB | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | CHB | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| NA18940 | hp1 | a0001 | c0001 | t0002 | g0223 | EAS | JPT | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0209 | EAS | JPT | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| NA18944 | hp1 | a0001 | c0001 | t0003 | g0243 | EAS | JPT | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0202 | EAS | JPT | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| NA18947 | hp1 | a0001 | c0001 | t0003 | g0240 | EAS | JPT | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| NA18952 | hp2 | a0001 | c0001 | t0005 | g0118 | EAS | JPT | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0218 | EAS | JPT | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| NA18956 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| NA18957 | hp1 | a0001 | c0001 | t0003 | g0256 | EAS | JPT | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| NA18960 | hp1 | a0001 | c0001 | t0005 | g0117 | EAS | JPT | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| NA18963 | hp2 | a0001 | c0001 | t0003 | g0255 | EAS | JPT | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0227 | EAS | JPT | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0217 | EAS | JPT | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| NA18968 | hp1 | a0001 | c0001 | t0003 | g0247 | EAS | JPT | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| NA18972 | hp1 | a0001 | c0001 | t0019 | g0248 | EAS | JPT | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| NA18974 | hp1 | a0001 | c0001 | t0003 | g0244 | EAS | JPT | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0221 | EAS | JPT | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0231 | EAS | JPT | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| NA18984 | hp2 | a0001 | c0001 | t0003 | g0258 | EAS | JPT | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| NA18985 | hp1 | a0001 | c0001 | t0003 | g0254 | EAS | JPT | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| NA18987 | hp1 | a0001 | c0001 | t0002 | g0198 | EAS | JPT | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0195 | EAS | JPT | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| NA18992 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| NA18993 | hp1 | a0001 | c0001 | t0003 | g0241 | EAS | JPT | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0204 | EAS | JPT | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| NA18997 | hp1 | a0001 | c0001 | t0021 | g0038 | EAS | JPT | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0232 | EAS | JPT | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| NA18999 | hp2 | a0001 | c0001 | t0017 | g0014 | EAS | JPT | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| NA19001 | hp1 | a0001 | c0001 | t0002 | g0216 | EAS | JPT | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| NA19002 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| NA19003 | hp2 | a0001 | c0001 | t0003 | g0259 | EAS | JPT | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| NA19007 | hp1 | a0001 | c0001 | t0003 | g0250 | EAS | JPT | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| NA19010 | hp2 | a0001 | c0001 | t0003 | g0238 | EAS | JPT | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0190 | EAS | JPT | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| NA19011 | hp2 | a0001 | c0001 | t0003 | g0237 | EAS | JPT | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| NA19030 | hp1 | a0001 | c0001 | t0024 | g0147 | AFR | LWK | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | LWK | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| NA19043 | hp1 | a0001 | c0001 | t0031 | g0148 | AFR | LWK | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| NA19043 | hp2 | a0001 | c0001 | t0004 | g0153 | AFR | LWK | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0215 | EAS | JPT | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0229 | EAS | JPT | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0230 | EAS | JPT | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| NA19064 | hp1 | a0001 | c0001 | t0003 | g0253 | EAS | JPT | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| NA19068 | hp1 | a0001 | c0001 | t0003 | g0245 | EAS | JPT | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| NA19075 | hp2 | a0001 | c0001 | t0003 | g0251 | EAS | JPT | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0200 | EAS | JPT | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0222 | EAS | JPT | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| NA19084 | hp1 | a0001 | c0001 | t0003 | g0257 | EAS | JPT | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0228 | EAS | JPT | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| NA19091 | hp1 | a0001 | c0001 | t0003 | g0239 | EAS | JPT | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| NA19240 | hp1 | a0001 | c0001 | t0004 | g0168 | AFR | YRI | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| NA19240 | hp2 | a0001 | c0001 | t0008 | g0135 | AFR | YRI | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0186 | AFR | ASW | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | ASW | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| NA20905 | hp1 | a0001 | c0001 | t0028 | g0185 | SAS | GIH | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0076 | SAS | GIH | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG02109 | hp1 | a0001 | c0001 | t0026 | g0246 | AFR | ACB | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0189 | AFR | ACB | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG02486 | hp1 | a0001 | c0001 | t0013 | g0171 | AFR | ACB | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG02559 | hp1 | a0001 | c0001 | t0006 | g0179 | AFR | ACB | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0084 | AFR | ACB | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG03471 | hp1 | a0001 | c0001 | t0004 | g0165 | AFR | MSL | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | MSL | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0206 | AFR | USA | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| NA20300 | hp2 | a0001 | c0001 | t0004 | g0155 | AFR | USA | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0017 | REF | REF | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0008 | g0004 | REF | REF | EEIG2_chr1_108555100_108644322 | EEIG2 | chr1 | 108555100 | 108644322 |
| 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 |
|---|
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:108560111 | AGCGGCGG others(14): Show |
A | 1 | a0001c0001t0016 | 2 | HG02258.hp2 HG02970.hp1 |
5_prime_UTR_variant | MODIFIER | c.-307_-287delAGGCGG others(15): Show |
EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/11 | 287 | INFO_REALIGN_3_PRIME | chr1 | 108560111 | |||||
| chr1:108560122 | A | AGGC | 3 | a0001c0001t0002 a0001c0001t0014 a0001c0001t0028 |
9 | HG01069.hp2 HG01071.hp2 HG01884.hp2 others(6): Show |
5_prime_UTR_variant | MODIFIER | c.-287_-285dupGCG | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/11 | 284 | INFO_REALIGN_3_PRIME | chr1 | 108560122 | |||||
| chr1:108560122 | A | AGGCGGCG others(5): Show |
3 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0006 |
34 | HG01070.hp1 HG01074.hp1 HG01934.hp2 others(31): Show |
5_prime_UTR_variant | MODIFIER | c.-296_-285dupGCGGCG others(6): Show |
EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/11 | 284 | INFO_REALIGN_3_PRIME | chr1 | 108560122 | |||||
| chr1:108560122 | A | AGGCGGCG others(8): Show |
2 | a0001c0001t0002 a0001c0001t0027 |
2 | HG02886.hp1 HG03491.hp1 |
5_prime_UTR_variant | MODIFIER | c.-299_-285dupGCGGCG others(9): Show |
EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/11 | 284 | INFO_REALIGN_3_PRIME | chr1 | 108560122 | |||||
| chr1:108560122 | A | AGGCGGCG others(14): Show |
1 | a0001c0001t0002 | 2 | HG00408.hp2 HG02027.hp2 |
5_prime_UTR_variant | MODIFIER | c.-305_-285dupGCGGCG others(15): Show |
EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/11 | 284 | INFO_REALIGN_3_PRIME | chr1 | 108560122 | |||||
| chr1:108560122 | AGGCGGCG others(2): Show |
A | 3 | a0001c0001t0002 a0001c0001t0029 a0001c0001t0030 |
25 | HG01361.hp2 HG01496.hp2 HG01928.hp1 others(22): Show |
5_prime_UTR_variant | MODIFIER | c.-293_-285delGCGGCG others(3): Show |
EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/11 | 285 | INFO_REALIGN_3_PRIME | chr1 | 108560122 | |||||
| chr1:108560172 | C | G | 2 | a0001c0001t0015 a0001c0001t0032 |
3 | HG02647.hp1 HG03453.hp2 NA18522.hp1 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-257C>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/11 | chr1 | 108560172 | |||||||
| chr1:108560256 | C | A | 1 | a0001c0001t0017 | 1 | NA18999.hp2 | 5_prime_UTR_variant | MODIFIER | c.-173C>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/11 | 173 | chr1 | 108560256 | ||||||
| chr1:108560276 | GCCCCGGC others(20): Show |
G | 1 | a0001c0001t0009 | 2 | HG01257.hp1 HG01258.hp1 |
5_prime_UTR_variant | MODIFIER | c.-141_-115delGCCGGC others(21): Show |
EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/11 | 115 | INFO_REALIGN_3_PRIME | chr1 | 108560276 | |||||
| chr1:108560277 | C | T | 2 | a0001c0001t0015 a0001c0001t0032 |
3 | HG02647.hp1 HG03453.hp2 NA18522.hp1 |
5_prime_UTR_variant | MODIFIER | c.-152C>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/11 | 152 | chr1 | 108560277 | ||||||
| chr1:108560290 | C | A | 1 | a0001c0001t0004 | 2 | HG02717.hp2 NA20300.hp2 |
5_prime_UTR_variant | MODIFIER | c.-139C>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/11 | 139 | chr1 | 108560290 | ||||||
| chr1:108560385 | G | GGCGCCCG others(5): Show |
1 | a0001c0001t0004 | 16 | HG01891.hp1 HG02145.hp2 HG02258.hp1 others(13): Show |
5_prime_UTR_variant | MODIFIER | c.-35_-34insTGTGCGCC others(4): Show |
EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/11 | 34 | INFO_REALIGN_3_PRIME | chr1 | 108560385 | |||||
| chr1:108560409 | G | T | 1 | a0001c0001t0004 | 16 | HG01891.hp1 HG02145.hp2 HG02258.hp1 others(13): Show |
5_prime_UTR_variant | MODIFIER | c.-20G>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/11 | 20 | chr1 | 108560409 | ||||||
| chr1:108635180 | G | A | 2 | a0001c0001t0010 a0001c0001t0018 |
3 | HG00735.hp1 HG01070.hp2 HG01071.hp1 |
3_prime_UTR_variant | MODIFIER | c.*30G>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 11/11 | 30 | chr1 | 108635180 | ||||||
| chr1:108635361 | GTGTGCCT others(10): Show |
G | 1 | a0001c0001t0011 | 2 | HG00738.hp1 HG01978.hp2 |
3_prime_UTR_variant | MODIFIER | c.*214_*230delTGCCTT others(11): Show |
EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 11/11 | 214 | INFO_REALIGN_3_PRIME | chr1 | 108635361 | |||||
| chr1:108635379 | T | G | 1 | a0001c0001t0011 | 2 | HG00738.hp1 HG01978.hp2 |
3_prime_UTR_variant | MODIFIER | c.*229T>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 11/11 | 229 | chr1 | 108635379 | ||||||
| chr1:108636093 | T | C | 1 | a0001c0001t0007 | 5 | HG02451.hp2 HG02647.hp2 HG03041.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*943T>C | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 11/11 | 943 | chr1 | 108636093 | ||||||
| chr1:108636215 | T | C | 1 | a0001c0001t0012 | 2 | HG02015.hp2 HG02027.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1065T>C | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 11/11 | 1065 | chr1 | 108636215 | ||||||
| chr1:108636385 | A | G | 1 | a0001c0001t0031 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1235A>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 11/11 | 1235 | chr1 | 108636385 | ||||||
| chr1:108636497 | T | C | 2 | a0001c0001t0003 a0001c0001t0019 |
25 | HG00423.hp1 HG02135.hp2 HG03669.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*1347T>C | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 11/11 | 1347 | chr1 | 108636497 | ||||||
| chr1:108636545 | A | T | 15 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0006 others(12): Show |
99 | HG00408.hp2 HG01069.hp2 HG01070.hp1 others(96): Show |
3_prime_UTR_variant | MODIFIER | c.*1395A>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 11/11 | 1395 | chr1 | 108636545 | ||||||
| chr1:108636790 | TG | T | 8 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0014 others(5): Show |
86 | HG00408.hp2 HG01069.hp2 HG01070.hp1 others(83): Show |
3_prime_UTR_variant | MODIFIER | c.*1641delG | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 11/11 | 1641 | chr1 | 108636790 | ||||||
| chr1:108636984 | A | G | 2 | a0001c0001t0029 a0001c0001t0030 |
2 | HG02630.hp1 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1834A>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 11/11 | 1834 | chr1 | 108636984 | ||||||
| chr1:108637036 | G | A | 1 | a0001c0001t0027 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1886G>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 11/11 | 1886 | chr1 | 108637036 | ||||||
| chr1:108637096 | G | A | 4 | a0001c0001t0024 a0001c0001t0025 a0001c0001t0031 others(1): Show |
4 | HG02055.hp1 NA18522.hp1 NA19030.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1946G>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 11/11 | 1946 | chr1 | 108637096 | ||||||
| chr1:108637149 | T | C | 8 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0014 others(5): Show |
86 | HG00408.hp2 HG01069.hp2 HG01070.hp1 others(83): Show |
3_prime_UTR_variant | MODIFIER | c.*1999T>C | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 11/11 | 1999 | chr1 | 108637149 | ||||||
| chr1:108637401 | G | A | 1 | a0001c0001t0032 | 1 | NA18522.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2251G>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 11/11 | 2251 | chr1 | 108637401 | ||||||
| chr1:108637416 | A | T | 8 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0014 others(5): Show |
86 | HG00408.hp2 HG01069.hp2 HG01070.hp1 others(83): Show |
3_prime_UTR_variant | MODIFIER | c.*2266A>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 11/11 | 2266 | chr1 | 108637416 | ||||||
| chr1:108637634 | T | A | 1 | a0001c0001t0020 | 1 | HG01943.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2484T>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 11/11 | 2484 | chr1 | 108637634 | ||||||
| chr1:108637711 | A | G | 1 | a0001c0001t0005 | 9 | HG01243.hp2 HG02015.hp1 HG02738.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2561A>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 11/11 | 2561 | chr1 | 108637711 | ||||||
| chr1:108637745 | A | G | 1 | a0001c0001t0023 | 1 | HG02896.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2595A>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 11/11 | 2595 | chr1 | 108637745 | ||||||
| chr1:108638475 | C | T | 1 | a0001c0001t0016 | 2 | HG02258.hp2 HG02970.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3325C>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 11/11 | 3325 | chr1 | 108638475 | ||||||
| chr1:108638527 | G | T | 2 | a0001c0001t0029 a0001c0001t0030 |
2 | HG02630.hp1 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3377G>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 11/11 | 3377 | chr1 | 108638527 | ||||||
| chr1:108638595 | G | A | 1 | a0001c0001t0029 | 1 | HG02630.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3445G>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 11/11 | 3445 | chr1 | 108638595 | ||||||
| chr1:108638682 | C | G | 4 | a0001c0001t0002 a0001c0001t0014 a0001c0001t0027 others(1): Show |
66 | HG00408.hp2 HG01069.hp2 HG01070.hp1 others(63): Show |
3_prime_UTR_variant | MODIFIER | c.*3532C>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 11/11 | 3532 | chr1 | 108638682 | ||||||
| chr1:108638687 | C | CAT | 31 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(28): Show |
266 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(263): Show |
3_prime_UTR_variant | MODIFIER | c.*3538_*3539dupAT | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 11/11 | 3540 | INFO_REALIGN_3_PRIME | chr1 | 108638687 | |||||
| chr1:108638829 | G | A | 2 | a0001c0001t0021 a0001c0001t0028 |
2 | NA18997.hp1 NA20905.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3679G>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 11/11 | 3679 | chr1 | 108638829 | ||||||
| chr1:108638857 | A | G | 1 | a0001c0001t0013 | 2 | HG02486.hp1 HG03130.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3707A>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 11/11 | 3707 | chr1 | 108638857 | ||||||
| chr1:108638995 | T | C | 1 | a0001c0001t0014 | 2 | HG01884.hp2 HG02976.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3845T>C | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 11/11 | 3845 | chr1 | 108638995 | ||||||
| chr1:108639231 | CT | C | 6 | a0001c0001t0018 a0001c0001t0019 a0001c0001t0022 others(3): Show |
6 | HG01070.hp2 HG01981.hp2 HG02109.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4097delT | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 11/11 | 4097 | INFO_REALIGN_3_PRIME | chr1 | 108639231 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:108560585 | G | T | 122 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0260 others(119): Show |
129 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(126): Show |
intron_variant | MODIFIER | c.137+20G>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108560585 | |||||||
| chr1:108560760 | A | T | 1 | a0001c0001t0032g0262 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.137+195A>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108560760 | |||||||
| chr1:108560980 | G | C | 2 | a0001c0001t0024g0147 a0001c0001t0031g0148 |
2 | NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.137+415G>C | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108560980 | |||||||
| chr1:108561374 | A | G | 1 | a0001c0001t0001g0146 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.137+809A>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108561374 | |||||||
| chr1:108561457 | C | G | 26 | a0001c0001t0001g0260 a0001c0001t0001g0261 a0001c0001t0003g0001 others(23): Show |
28 | HG00408.hp1 HG00423.hp1 HG02109.hp1 others(25): Show |
intron_variant | MODIFIER | c.137+892C>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108561457 | |||||||
| chr1:108561492 | A | G | 1 | a0001c0001t0031g0148 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.137+927A>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108561492 | |||||||
| chr1:108561500 | T | G | 1 | a0001c0001t0001g0010 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.137+935T>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108561500 | |||||||
| chr1:108561580 | CT | C | 7 | a0001c0001t0004g0149 a0001c0001t0004g0150 a0001c0001t0004g0151 others(4): Show |
7 | HG02572.hp1 HG02717.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.137+1017delT | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 108561580 | ||||||
| chr1:108561684 | A | G | 1 | a0001c0001t0001g0145 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.137+1119A>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108561684 | |||||||
| chr1:108561784 | A | G | 120 | a0001c0001t0001g0260 a0001c0001t0001g0261 a0001c0001t0002g0005 others(117): Show |
127 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(124): Show |
intron_variant | MODIFIER | c.137+1219A>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108561784 | |||||||
| chr1:108561853 | T | C | 1 | a0001c0001t0001g0011 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.137+1288T>C | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108561853 | |||||||
| chr1:108561890 | G | A | 4 | a0001c0001t0004g0149 a0001c0001t0004g0150 a0001c0001t0004g0151 others(1): Show |
4 | HG02572.hp1 HG02809.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.137+1325G>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108561890 | |||||||
| chr1:108562120 | C | T | 2 | a0001c0001t0001g0144 a0001c0001t0002g0236 |
2 | HG02698.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.137+1555C>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108562120 | |||||||
| chr1:108562323 | C | T | 65 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(62): Show |
70 | HG00408.hp2 HG01069.hp2 HG01070.hp1 others(67): Show |
intron_variant | MODIFIER | c.137+1758C>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108562323 | |||||||
| chr1:108562471 | G | A | 1 | a0001c0001t0006g0158 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.137+1906G>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108562471 | |||||||
| chr1:108563056 | A | C | 2 | a0001c0001t0001g0142 a0001c0001t0001g0143 |
2 | HG02165.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.137+2491A>C | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108563056 | |||||||
| chr1:108563191 | A | G | 1 | a0001c0001t0031g0148 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.137+2626A>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108563191 | |||||||
| chr1:108563209 | G | A | 1 | a0001c0001t0001g0012 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.137+2644G>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108563209 | |||||||
| chr1:108563222 | G | A | 67 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(64): Show |
72 | HG00408.hp2 HG01069.hp2 HG01070.hp1 others(69): Show |
intron_variant | MODIFIER | c.137+2657G>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108563222 | |||||||
| chr1:108563244 | A | G | 2 | a0001c0001t0016g0159 a0001c0001t0016g0160 |
2 | HG02258.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.137+2679A>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108563244 | |||||||
| chr1:108563354 | T | G | 2 | a0001c0001t0016g0159 a0001c0001t0016g0160 |
2 | HG02258.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.137+2789T>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108563354 | |||||||
| chr1:108563403 | A | G | 1 | a0001c0001t0001g0141 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.137+2838A>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108563403 | |||||||
| chr1:108563909 | A | G | 65 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(62): Show |
70 | HG00408.hp2 HG01069.hp2 HG01070.hp1 others(67): Show |
intron_variant | MODIFIER | c.137+3344A>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108563909 | |||||||
| chr1:108563961 | G | A | 2 | a0001c0001t0016g0159 a0001c0001t0016g0160 |
2 | HG02258.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.137+3396G>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108563961 | |||||||
| chr1:108563968 | T | C | 30 | a0001c0001t0001g0260 a0001c0001t0001g0261 a0001c0001t0003g0001 others(27): Show |
32 | HG00408.hp1 HG00423.hp1 HG02055.hp1 others(29): Show |
intron_variant | MODIFIER | c.137+3403T>C | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108563968 | |||||||
| chr1:108564143 | C | T | 2 | a0001c0001t0004g0154 a0001c0001t0004g0155 |
2 | HG02717.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.137+3578C>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108564143 | |||||||
| chr1:108564172 | C | G | 26 | a0001c0001t0001g0260 a0001c0001t0001g0261 a0001c0001t0003g0001 others(23): Show |
28 | HG00408.hp1 HG00423.hp1 HG02109.hp1 others(25): Show |
intron_variant | MODIFIER | c.137+3607C>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108564172 | |||||||
| chr1:108564212 | C | T | 2 | a0001c0001t0016g0159 a0001c0001t0016g0160 |
2 | HG02258.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.137+3647C>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108564212 | |||||||
| chr1:108564405 | G | A | 1 | a0001c0001t0002g0177 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.137+3840G>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108564405 | |||||||
| chr1:108564462 | G | A | 1 | a0001c0001t0022g0013 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.137+3897G>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108564462 | |||||||
| chr1:108564848 | G | C | 80 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(77): Show |
85 | HG00408.hp2 HG01069.hp2 HG01070.hp1 others(82): Show |
intron_variant | MODIFIER | c.137+4283G>C | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108564848 | |||||||
| chr1:108564872 | G | C | 9 | a0001c0001t0003g0237 a0001c0001t0003g0238 a0001c0001t0003g0239 others(6): Show |
9 | HG00423.hp1 NA18944.hp1 NA18947.hp1 others(6): Show |
intron_variant | MODIFIER | c.137+4307G>C | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108564872 | |||||||
| chr1:108564876 | G | A | 2 | a0001c0001t0001g0015 a0001c0001t0017g0014 |
2 | NA18940.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.137+4311G>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108564876 | |||||||
| chr1:108564914 | C | T | 80 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(77): Show |
85 | HG00408.hp2 HG01069.hp2 HG01070.hp1 others(82): Show |
intron_variant | MODIFIER | c.137+4349C>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108564914 | |||||||
| chr1:108565338 | T | G | 1 | a0001c0001t0013g0171 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.137+4773T>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108565338 | |||||||
| chr1:108565546 | A | G | 1 | a0001c0001t0013g0171 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.137+4981A>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108565546 | |||||||
| chr1:108565773 | G | A | 16 | a0001c0001t0001g0016 a0001c0001t0001g0022 a0001c0001t0001g0024 others(13): Show |
16 | HG00738.hp1 HG01257.hp1 HG01258.hp1 others(13): Show |
intron_variant | MODIFIER | c.137+5208G>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108565773 | |||||||
| chr1:108565817 | C | T | 4 | a0001c0001t0001g0137 a0001c0001t0001g0138 a0001c0001t0001g0139 others(1): Show |
4 | NA18747.hp2 NA18950.hp1 NA18995.hp1 others(1): Show |
intron_variant | MODIFIER | c.137+5252C>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108565817 | |||||||
| chr1:108566102 | C | T | 2 | a0001c0001t0001g0030 a0001c0001t0001g0031 |
2 | HG03942.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.137+5537C>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108566102 | |||||||
| chr1:108566144 | G | A | 228 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(225): Show |
234 | HG00408.hp2 HG00423.hp2 HG00639.hp1 others(231): Show |
intron_variant | MODIFIER | c.137+5579G>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108566144 | |||||||
| chr1:108566145 | G | A | 2 | a0001c0001t0016g0159 a0001c0001t0016g0160 |
2 | HG02258.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.137+5580G>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108566145 | |||||||
| chr1:108566162 | G | T | 1 | a0001c0001t0001g0133 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.137+5597G>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108566162 | |||||||
| chr1:108566558 | G | T | 2 | a0001c0001t0014g0234 a0001c0001t0014g0235 |
2 | HG01884.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.137+5993G>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108566558 | |||||||
| chr1:108566580 | T | C | 258 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(255): Show |
266 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(263): Show |
intron_variant | MODIFIER | c.137+6015T>C | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108566580 | |||||||
| chr1:108566696 | T | A | 2 | a0001c0001t0016g0159 a0001c0001t0016g0160 |
2 | HG02258.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.137+6131T>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108566696 | |||||||
| chr1:108566765 | G | T | 1 | a0001c0001t0001g0003 | 2 | NA18953.hp1 NA18956.hp2 |
intron_variant | MODIFIER | c.137+6200G>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108566765 | |||||||
| chr1:108566800 | C | T | 1 | a0001c0001t0023g0132 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.137+6235C>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108566800 | |||||||
| chr1:108566883 | G | A | 3 | a0001c0001t0015g0172 a0001c0001t0015g0173 a0001c0001t0032g0262 |
3 | HG02647.hp1 HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.137+6318G>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108566883 | |||||||
| chr1:108567156 | A | G | 1 | a0001c0001t0001g0131 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.137+6591A>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108567156 | |||||||
| chr1:108567166 | A | T | 2 | a0001c0001t0016g0159 a0001c0001t0016g0160 |
2 | HG02258.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.137+6601A>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108567166 | |||||||
| chr1:108567167 | T | A | 1 | a0001c0001t0001g0032 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.137+6602T>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108567167 | |||||||
| chr1:108567204 | A | C | 1 | a0001c0001t0001g0130 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.137+6639A>C | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108567204 | |||||||
| chr1:108567276 | G | A | 2 | a0001c0001t0016g0159 a0001c0001t0016g0160 |
2 | HG02258.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.137+6711G>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108567276 | |||||||
| chr1:108567374 | C | G | 2 | a0001c0001t0016g0159 a0001c0001t0016g0160 |
2 | HG02258.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.137+6809C>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108567374 | |||||||
| chr1:108567376 | A | G | 1 | a0001c0001t0013g0176 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.137+6811A>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108567376 | |||||||
| chr1:108567470 | G | A | 9 | a0001c0001t0004g0162 a0001c0001t0004g0163 a0001c0001t0004g0164 others(6): Show |
9 | HG01891.hp1 HG02145.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.137+6905G>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108567470 | |||||||
| chr1:108567714 | C | T | 3 | a0001c0001t0015g0172 a0001c0001t0015g0173 a0001c0001t0032g0262 |
3 | HG02647.hp1 HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.137+7149C>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108567714 | |||||||
| chr1:108567715 | G | C | 2 | a0001c0001t0016g0159 a0001c0001t0016g0160 |
2 | HG02258.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.137+7150G>C | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108567715 | |||||||
| chr1:108567766 | A | G | 1 | a0001c0001t0002g0233 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.137+7201A>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108567766 | |||||||
| chr1:108567792 | A | T | 1 | a0001c0001t0002g0233 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.137+7227A>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108567792 | |||||||
| chr1:108567886 | T | A | 4 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(1): Show |
4 | HG01169.hp2 HG03491.hp2 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.137+7321T>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108567886 | |||||||
| chr1:108567941 | A | G | 142 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(139): Show |
143 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(140): Show |
intron_variant | MODIFIER | c.137+7376A>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108567941 | |||||||
| chr1:108568239 | G | A | 3 | a0001c0001t0006g0178 a0001c0001t0006g0179 a0001c0001t0006g0180 |
3 | HG02559.hp1 HG02886.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.137+7674G>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108568239 | |||||||
| chr1:108568294 | A | G | 44 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0002g0191 others(41): Show |
46 | HG00408.hp2 HG01070.hp1 HG01074.hp1 others(43): Show |
intron_variant | MODIFIER | c.137+7729A>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108568294 | |||||||
| chr1:108568390 | A | G | 1 | a0001c0001t0001g0129 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.137+7825A>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108568390 | |||||||
| chr1:108568667 | A | T | 1 | a0001c0001t0003g0259 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.137+8102A>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108568667 | |||||||
| chr1:108568935 | G | A | 1 | a0001c0001t0023g0132 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.137+8370G>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108568935 | |||||||
| chr1:108568956 | G | A | 2 | a0001c0001t0016g0159 a0001c0001t0016g0160 |
2 | HG02258.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.137+8391G>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108568956 | |||||||
| chr1:108569651 | T | C | 1 | a0001c0001t0001g0037 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.137+9086T>C | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108569651 | |||||||
| chr1:108569670 | C | T | 258 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(255): Show |
266 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(263): Show |
intron_variant | MODIFIER | c.137+9105C>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108569670 | |||||||
| chr1:108569675 | C | A | 16 | a0001c0001t0004g0149 a0001c0001t0004g0150 a0001c0001t0004g0151 others(13): Show |
16 | HG01891.hp1 HG02145.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.137+9110C>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108569675 | |||||||
| chr1:108569712 | C | A | 2 | a0001c0001t0001g0130 a0001c0001t0021g0038 |
2 | NA18992.hp2 NA18997.hp1 |
intron_variant | MODIFIER | c.137+9147C>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108569712 | |||||||
| chr1:108570038 | A | G | 1 | a0001c0001t0013g0171 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.137+9473A>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108570038 | |||||||
| chr1:108570113 | A | C | 2 | a0001c0001t0006g0179 a0001c0001t0006g0180 |
2 | HG02559.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.137+9548A>C | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108570113 | |||||||
| chr1:108570208 | T | A | 2 | a0001c0001t0016g0159 a0001c0001t0016g0160 |
2 | HG02258.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.137+9643T>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108570208 | |||||||
| chr1:108570338 | A | G | 3 | a0001c0001t0002g0190 a0001c0001t0002g0233 a0001c0001t0002g0236 |
3 | HG03669.hp1 HG04199.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.137+9773A>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108570338 | |||||||
| chr1:108570469 | T | G | 5 | a0001c0001t0006g0178 a0001c0001t0006g0179 a0001c0001t0006g0180 others(2): Show |
5 | HG02559.hp1 HG02886.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.137+9904T>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108570469 | |||||||
| chr1:108570562 | A | G | 81 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(78): Show |
86 | HG00408.hp2 HG01069.hp2 HG01070.hp1 others(83): Show |
intron_variant | MODIFIER | c.137+9997A>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108570562 | |||||||
| chr1:108570841 | T | C | 81 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(78): Show |
86 | HG00408.hp2 HG01069.hp2 HG01070.hp1 others(83): Show |
intron_variant | MODIFIER | c.137+10276T>C | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108570841 | |||||||
| chr1:108570864 | C | T | 4 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 others(1): Show |
4 | NA18964.hp2 NA18981.hp2 NA18994.hp2 others(1): Show |
intron_variant | MODIFIER | c.137+10299C>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108570864 | |||||||
| chr1:108570956 | C | T | 4 | a0001c0001t0005g0121 a0001c0001t0005g0122 a0001c0001t0005g0123 others(1): Show |
4 | HG02738.hp2 HG03710.hp2 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.137+10391C>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108570956 | |||||||
| chr1:108571059 | G | A | 1 | a0001c0001t0002g0191 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.137+10494G>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108571059 | |||||||
| chr1:108571155 | C | G | 3 | a0001c0001t0010g0002 a0001c0001t0010g0120 a0001c0001t0018g0002 |
3 | HG00735.hp1 HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.137+10590C>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108571155 | |||||||
| chr1:108571525 | G | T | 1 | a0001c0001t0013g0176 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.137+10960G>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108571525 | |||||||
| chr1:108571730 | G | A | 2 | a0001c0001t0001g0039 a0001c0001t0001g0040 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.137+11165G>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108571730 | |||||||
| chr1:108571786 | C | T | 1 | a0001c0001t0001g0119 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.137+11221C>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108571786 | |||||||
| chr1:108571810 | A | G | 2 | a0001c0001t0016g0159 a0001c0001t0016g0160 |
2 | HG02258.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.137+11245A>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108571810 | |||||||
| chr1:108571854 | A | G | 81 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(78): Show |
86 | HG00408.hp2 HG01069.hp2 HG01070.hp1 others(83): Show |
intron_variant | MODIFIER | c.137+11289A>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108571854 | |||||||
| chr1:108571867 | G | A | 81 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(78): Show |
86 | HG00408.hp2 HG01069.hp2 HG01070.hp1 others(83): Show |
intron_variant | MODIFIER | c.137+11302G>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108571867 | |||||||
| chr1:108571981 | A | C | 2 | a0001c0001t0024g0147 a0001c0001t0031g0148 |
2 | NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.137+11416A>C | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108571981 | |||||||
| chr1:108572111 | C | T | 2 | a0001c0001t0016g0159 a0001c0001t0016g0160 |
2 | HG02258.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.137+11546C>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108572111 | |||||||
| chr1:108572162 | T | C | 1 | a0001c0001t0032g0262 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.137+11597T>C | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108572162 | |||||||
| chr1:108572216 | T | A | 1 | a0001c0001t0013g0171 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.137+11651T>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108572216 | |||||||
| chr1:108572221 | A | G | 9 | a0001c0001t0005g0114 a0001c0001t0005g0115 a0001c0001t0005g0116 others(6): Show |
9 | HG01243.hp2 HG02015.hp1 HG02738.hp2 others(6): Show |
intron_variant | MODIFIER | c.137+11656A>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108572221 | |||||||
| chr1:108572260 | T | C | 2 | a0001c0001t0016g0159 a0001c0001t0016g0160 |
2 | HG02258.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.137+11695T>C | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108572260 | |||||||
| chr1:108572638 | C | T | 1 | a0001c0001t0007g0029 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.137+12073C>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108572638 | |||||||
| chr1:108572667 | G | A | 3 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 |
3 | NA18950.hp2 NA18969.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.137+12102G>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108572667 | |||||||
| chr1:108572684 | C | T | 2 | a0001c0001t0016g0159 a0001c0001t0016g0160 |
2 | HG02258.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.137+12119C>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108572684 | |||||||
| chr1:108572982 | T | C | 2 | a0001c0001t0029g0174 a0001c0001t0030g0175 |
2 | HG02630.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.137+12417T>C | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108572982 | |||||||
| chr1:108573139 | T | A | 81 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(78): Show |
86 | HG00408.hp2 HG01069.hp2 HG01070.hp1 others(83): Show |
intron_variant | MODIFIER | c.137+12574T>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108573139 | |||||||
| chr1:108573169 | G | A | 1 | a0001c0001t0026g0246 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.137+12604G>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108573169 | |||||||
| chr1:108573339 | C | T | 1 | a0001c0001t0001g0141 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.137+12774C>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108573339 | |||||||
| chr1:108573445 | A | G | 2 | a0001c0001t0016g0159 a0001c0001t0016g0160 |
2 | HG02258.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.137+12880A>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108573445 | |||||||
| chr1:108573447 | A | G | 141 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(138): Show |
142 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(139): Show |
intron_variant | MODIFIER | c.137+12882A>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108573447 | |||||||
| chr1:108573453 | T | C | 2 | a0001c0001t0014g0234 a0001c0001t0014g0235 |
2 | HG01884.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.137+12888T>C | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108573453 | |||||||
| chr1:108573561 | C | T | 2 | a0001c0001t0016g0159 a0001c0001t0016g0160 |
2 | HG02258.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.137+12996C>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108573561 | |||||||
| chr1:108573641 | G | A | 7 | a0001c0001t0004g0149 a0001c0001t0004g0150 a0001c0001t0004g0151 others(4): Show |
7 | HG02572.hp1 HG02717.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.137+13076G>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108573641 | |||||||
| chr1:108573726 | A | G | 2 | a0001c0001t0001g0113 a0001c0001t0001g0145 |
2 | HG01069.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.137+13161A>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108573726 | |||||||
| chr1:108573858 | T | C | 1 | a0001c0001t0013g0171 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.137+13293T>C | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108573858 | |||||||
| chr1:108573894 | G | A | 1 | a0001c0001t0001g0144 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.137+13329G>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108573894 | |||||||
| chr1:108573995 | T | G | 1 | a0001c0001t0006g0158 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.137+13430T>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108573995 | |||||||
| chr1:108574257 | C | CA | 84 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(81): Show |
89 | HG00408.hp2 HG00735.hp1 HG01069.hp2 others(86): Show |
intron_variant | MODIFIER | c.137+13702dupA | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 108574257 | ||||||
| chr1:108574510 | G | A | 2 | a0001c0001t0001g0030 a0001c0001t0001g0031 |
2 | HG03942.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.137+13945G>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108574510 | |||||||
| chr1:108574530 | C | G | 1 | a0001c0001t0002g0232 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.137+13965C>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108574530 | |||||||
| chr1:108574713 | G | A | 44 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0002g0191 others(41): Show |
46 | HG00408.hp2 HG01070.hp1 HG01074.hp1 others(43): Show |
intron_variant | MODIFIER | c.137+14148G>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108574713 | |||||||
| chr1:108574760 | G | C | 1 | a0001c0001t0029g0174 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.137+14195G>C | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108574760 | |||||||
| chr1:108574891 | C | T | 1 | a0001c0001t0001g0012 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.137+14326C>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108574891 | |||||||
| chr1:108574964 | G | A | 81 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(78): Show |
86 | HG00408.hp2 HG01069.hp2 HG01070.hp1 others(83): Show |
intron_variant | MODIFIER | c.137+14399G>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108574964 | |||||||
| chr1:108575165 | A | G | 2 | a0001c0001t0016g0159 a0001c0001t0016g0160 |
2 | HG02258.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.137+14600A>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108575165 | |||||||
| chr1:108575314 | A | T | 2 | a0001c0001t0016g0159 a0001c0001t0016g0160 |
2 | HG02258.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.137+14749A>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108575314 | |||||||
| chr1:108575334 | C | T | 2 | a0001c0001t0014g0234 a0001c0001t0014g0235 |
2 | HG01884.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.137+14769C>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108575334 | |||||||
| chr1:108575425 | A | G | 2 | a0001c0001t0001g0127 a0001c0001t0001g0128 |
2 | NA18994.hp2 NA18997.hp2 |
intron_variant | MODIFIER | c.137+14860A>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108575425 | |||||||
| chr1:108575579 | G | T | 9 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0001t0001g0107 others(6): Show |
9 | HG02040.hp1 NA18947.hp2 NA18960.hp2 others(6): Show |
intron_variant | MODIFIER | c.137+15014G>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108575579 | |||||||
| chr1:108575799 | G | A | 1 | a0001c0001t0001g0144 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.137+15234G>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108575799 | |||||||
| chr1:108575836 | A | G | 6 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0101 others(3): Show |
6 | HG00642.hp1 HG02055.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.137+15271A>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108575836 | |||||||
| chr1:108575848 | G | A | 2 | a0001c0001t0016g0159 a0001c0001t0016g0160 |
2 | HG02258.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.137+15283G>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108575848 | |||||||
| chr1:108575893 | A | G | 2 | a0001c0001t0016g0159 a0001c0001t0016g0160 |
2 | HG02258.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.137+15328A>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108575893 | |||||||
| chr1:108575932 | A | C | 2 | a0001c0001t0016g0159 a0001c0001t0016g0160 |
2 | HG02258.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.137+15367A>C | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108575932 | |||||||
| chr1:108575942 | AGATAT | A | 81 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(78): Show |
86 | HG00408.hp2 HG01069.hp2 HG01070.hp1 others(83): Show |
intron_variant | MODIFIER | c.137+15384_137+1538 others(9): Show |
EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 108575942 | ||||||
| chr1:108576308 | T | A | 1 | a0001c0001t0006g0158 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.137+15743T>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108576308 | |||||||
| chr1:108576359 | A | C | 2 | a0001c0001t0002g0230 a0001c0001t0002g0231 |
2 | NA18981.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.137+15794A>C | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108576359 | |||||||
| chr1:108576447 | T | C | 2 | a0001c0001t0001g0044 a0001c0001t0002g0192 |
2 | HG01496.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.137+15882T>C | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108576447 | |||||||
| chr1:108576453 | C | G | 16 | a0001c0001t0004g0149 a0001c0001t0004g0150 a0001c0001t0004g0151 others(13): Show |
16 | HG01891.hp1 HG02145.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.137+15888C>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108576453 | |||||||
| chr1:108576482 | T | C | 1 | a0001c0001t0002g0193 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.137+15917T>C | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108576482 | |||||||
| chr1:108576531 | G | A | 1 | a0001c0001t0023g0132 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.137+15966G>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108576531 | |||||||
| chr1:108576646 | A | G | 1 | a0001c0001t0013g0171 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.137+16081A>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108576646 | |||||||
| chr1:108576695 | A | G | 2 | a0001c0001t0011g0027 a0001c0001t0011g0028 |
2 | HG00738.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.137+16130A>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108576695 | |||||||
| chr1:108576758 | C | A | 1 | a0001c0001t0003g0237 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.137+16193C>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108576758 | |||||||
| chr1:108576922 | G | A | 1 | a0001c0001t0013g0171 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.137+16357G>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108576922 | |||||||
| chr1:108577059 | A | G | 1 | a0001c0001t0002g0229 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.137+16494A>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108577059 | |||||||
| chr1:108577071 | A | G | 2 | a0001c0001t0001g0099 a0001c0001t0001g0100 |
2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.137+16506A>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108577071 | |||||||
| chr1:108577124 | G | A | 140 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(137): Show |
141 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(138): Show |
intron_variant | MODIFIER | c.137+16559G>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108577124 | |||||||
| chr1:108577126 | C | T | 1 | a0001c0001t0004g0170 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.137+16561C>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108577126 | |||||||
| chr1:108577170 | G | T | 2 | a0001c0001t0016g0159 a0001c0001t0016g0160 |
2 | HG02258.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.137+16605G>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108577170 | |||||||
| chr1:108577424 | GT | G | 232 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(229): Show |
238 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(235): Show |
intron_variant | MODIFIER | c.137+16864delT | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 108577424 | ||||||
| chr1:108577611 | G | T | 2 | a0001c0001t0016g0159 a0001c0001t0016g0160 |
2 | HG02258.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.137+17046G>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108577611 | |||||||
| chr1:108577681 | A | T | 1 | a0001c0001t0031g0148 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.137+17116A>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108577681 | |||||||
| chr1:108577711 | A | C | 1 | a0001c0001t0029g0174 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.137+17146A>C | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108577711 | |||||||
| chr1:108577731 | A | G | 141 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(138): Show |
142 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(139): Show |
intron_variant | MODIFIER | c.137+17166A>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108577731 | |||||||
| chr1:108577744 | T | A | 1 | a0001c0001t0027g0183 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.137+17179T>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108577744 | |||||||
| chr1:108577825 | A | G | 16 | a0001c0001t0004g0149 a0001c0001t0004g0150 a0001c0001t0004g0151 others(13): Show |
16 | HG01891.hp1 HG02145.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.137+17260A>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108577825 | |||||||
| chr1:108577829 | T | A | 1 | a0001c0001t0002g0229 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.137+17264T>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108577829 | |||||||
| chr1:108577873 | A | T | 2 | a0001c0001t0001g0098 a0001c0001t0002g0097 |
2 | HG01978.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.137+17308A>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108577873 | |||||||
| chr1:108577878 | A | G | 1 | a0001c0001t0025g0161 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.137+17313A>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108577878 | |||||||
| chr1:108577899 | T | A | 2 | a0001c0001t0016g0159 a0001c0001t0016g0160 |
2 | HG02258.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.137+17334T>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108577899 | |||||||
| chr1:108577948 | G | A | 2 | a0001c0001t0016g0159 a0001c0001t0016g0160 |
2 | HG02258.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.137+17383G>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108577948 | |||||||
| chr1:108578214 | T | C | 8 | a0001c0001t0002g0005 a0001c0001t0002g0184 a0001c0001t0002g0190 others(5): Show |
9 | HG01069.hp2 HG01071.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.137+17649T>C | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108578214 | |||||||
| chr1:108578239 | C | G | 3 | a0001c0001t0015g0172 a0001c0001t0015g0173 a0001c0001t0032g0262 |
3 | HG02647.hp1 HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.137+17674C>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108578239 | |||||||
| chr1:108578348 | C | T | 5 | a0001c0001t0015g0172 a0001c0001t0015g0173 a0001c0001t0029g0174 others(2): Show |
5 | HG02630.hp1 HG02647.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.137+17783C>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108578348 | |||||||
| chr1:108578349 | G | A | 3 | a0001c0001t0015g0172 a0001c0001t0015g0173 a0001c0001t0032g0262 |
3 | HG02647.hp1 HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.137+17784G>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108578349 | |||||||
| chr1:108578648 | G | A | 81 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(78): Show |
86 | HG00408.hp2 HG01069.hp2 HG01070.hp1 others(83): Show |
intron_variant | MODIFIER | c.137+18083G>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108578648 | |||||||
| chr1:108578964 | G | A | 2 | a0001c0001t0024g0147 a0001c0001t0031g0148 |
2 | NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.137+18399G>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108578964 | |||||||
| chr1:108579157 | A | T | 1 | a0001c0001t0003g0245 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.137+18592A>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108579157 | |||||||
| chr1:108579279 | T | G | 225 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(222): Show |
231 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(228): Show |
intron_variant | MODIFIER | c.137+18714T>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108579279 | |||||||
| chr1:108579324 | A | T | 2 | a0001c0001t0016g0159 a0001c0001t0016g0160 |
2 | HG02258.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.137+18759A>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108579324 | |||||||
| chr1:108579343 | A | T | 141 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(138): Show |
142 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(139): Show |
intron_variant | MODIFIER | c.137+18778A>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108579343 | |||||||
| chr1:108579365 | G | A | 81 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(78): Show |
86 | HG00408.hp2 HG01069.hp2 HG01070.hp1 others(83): Show |
intron_variant | MODIFIER | c.137+18800G>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108579365 | |||||||
| chr1:108579382 | G | A | 1 | a0001c0001t0001g0045 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.137+18817G>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108579382 | |||||||
| chr1:108579526 | A | G | 2 | a0001c0001t0011g0027 a0001c0001t0011g0028 |
2 | HG00738.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.137+18961A>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108579526 | |||||||
| chr1:108579582 | A | G | 2 | a0001c0001t0029g0174 a0001c0001t0030g0175 |
2 | HG02630.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.137+19017A>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108579582 | |||||||
| chr1:108579585 | C | T | 2 | a0001c0001t0016g0159 a0001c0001t0016g0160 |
2 | HG02258.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.137+19020C>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108579585 | |||||||
| chr1:108579586 | G | A | 141 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(138): Show |
142 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(139): Show |
intron_variant | MODIFIER | c.137+19021G>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108579586 | |||||||
| chr1:108579689 | C | T | 1 | a0001c0001t0004g0152 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.137+19124C>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108579689 | |||||||
| chr1:108579738 | G | GGT | 20 | a0001c0001t0003g0001 a0001c0001t0003g0237 a0001c0001t0003g0238 others(17): Show |
22 | HG00423.hp1 HG01891.hp2 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.137+19207_137+1920 others(6): Show |
EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 108579738 | ||||||
| chr1:108579738 | G | GGTGT | 6 | a0001c0001t0003g0244 a0001c0001t0003g0257 a0001c0001t0003g0258 others(3): Show |
6 | HG02258.hp2 HG02970.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.137+19205_137+1920 others(8): Show |
EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 108579738 | ||||||
| chr1:108579766 | T | TGAGAGAG others(9): Show |
1 | a0001c0001t0001g0032 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.137+19202_137+1920 others(20): Show |
EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 108579766 | ||||||
| chr1:108579768 | T | A | 1 | a0001c0001t0001g0032 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.137+19203T>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108579768 | |||||||
| chr1:108579770 | T | A | 2 | a0001c0001t0001g0032 a0001c0001t0001g0260 |
2 | HG00408.hp1 HG00639.hp1 |
intron_variant | MODIFIER | c.137+19205T>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108579770 | |||||||
| chr1:108579770 | T | TGAGAGAG others(3): Show |
1 | a0001c0001t0001g0046 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.137+19206_137+1920 others(14): Show |
EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 108579770 | ||||||
| chr1:108579770 | T | TGAGAGAG others(5): Show |
1 | a0001c0001t0002g0194 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.137+19206_137+1920 others(16): Show |
EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 108579770 | ||||||
| chr1:108579770 | T | TGAGAGAG others(13): Show |
1 | a0001c0001t0021g0038 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.137+19206_137+1920 others(24): Show |
EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 108579770 | ||||||
| chr1:108579770 | T | TGAGAGAG others(17): Show |
2 | a0001c0001t0001g0016 a0001c0001t0001g0047 |
2 | HG02622.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.137+19206_137+1920 others(28): Show |
EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 108579770 | ||||||
| chr1:108579772 | T | A | 7 | a0001c0001t0001g0016 a0001c0001t0001g0032 a0001c0001t0001g0046 others(4): Show |
7 | HG00408.hp1 HG00639.hp1 HG01981.hp1 others(4): Show |
intron_variant | MODIFIER | c.137+19207T>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108579772 | |||||||
| chr1:108579772 | T | TGAGAGAG others(5): Show |
41 | a0001c0001t0001g0037 a0001c0001t0001g0041 a0001c0001t0001g0042 others(38): Show |
41 | HG00408.hp2 HG00423.hp2 HG00639.hp2 others(38): Show |
intron_variant | MODIFIER | c.137+19220_137+1923 others(16): Show |
EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 108579772 | ||||||
| chr1:108579772 | T | TGAGAGAG others(7): Show |
8 | a0001c0001t0001g0069 a0001c0001t0001g0098 a0001c0001t0001g0099 others(5): Show |
8 | HG01256.hp1 HG01258.hp2 HG01981.hp2 others(5): Show |
intron_variant | MODIFIER | c.137+19218_137+1923 others(18): Show |
EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 108579772 | ||||||
| chr1:108579772 | T | TGAGAGAG others(9): Show |
6 | a0001c0001t0001g0071 a0001c0001t0001g0126 a0001c0001t0002g0197 others(3): Show |
6 | HG00735.hp1 HG01070.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.137+19216_137+1923 others(20): Show |
EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 108579772 | ||||||
| chr1:108579772 | T | TGAGAGAG others(11): Show |
4 | a0001c0001t0001g0072 a0001c0001t0007g0019 a0001c0001t0007g0020 others(1): Show |
4 | HG01884.hp1 HG02451.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.137+19214_137+1923 others(22): Show |
EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 108579772 | ||||||
| chr1:108579772 | T | TGAGAGAG others(13): Show |
4 | a0001c0001t0001g0030 a0001c0001t0001g0033 a0001c0001t0001g0073 others(1): Show |
4 | HG01169.hp2 HG01952.hp2 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.137+19212_137+1923 others(24): Show |
EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 108579772 | ||||||
| chr1:108579772 | T | TGAGAGAG others(15): Show |
4 | a0001c0001t0001g0010 a0001c0001t0001g0074 a0001c0001t0001g0113 others(1): Show |
4 | HG01069.hp1 HG01256.hp2 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.137+19210_137+1923 others(26): Show |
EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 108579772 | ||||||
| chr1:108579772 | T | TGAGAGAG others(17): Show |
5 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0075 others(2): Show |
5 | HG02698.hp1 HG03491.hp2 HG03492.hp2 others(2): Show |
intron_variant | MODIFIER | c.137+19208_137+1923 others(28): Show |
EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 108579772 | ||||||
| chr1:108579772 | T | TGAGAGAG others(19): Show |
8 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0078 others(5): Show |
8 | HG00738.hp1 HG01257.hp1 HG01975.hp1 others(5): Show |
intron_variant | MODIFIER | c.137+19231_137+1923 others(30): Show |
EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 108579772 | ||||||
| chr1:108579772 | T | TGAGAGAG others(21): Show |
8 | a0001c0001t0001g0015 a0001c0001t0001g0022 a0001c0001t0001g0044 others(5): Show |
8 | HG00738.hp2 HG01106.hp2 HG02004.hp1 others(5): Show |
intron_variant | MODIFIER | c.137+19231_137+1923 others(32): Show |
EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 108579772 | ||||||
| chr1:108579772 | T | TGAGAGAG others(23): Show |
6 | a0001c0001t0001g0011 a0001c0001t0001g0024 a0001c0001t0001g0025 others(3): Show |
6 | HG01934.hp1 HG02965.hp2 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.137+19231_137+1923 others(34): Show |
EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 108579772 | ||||||
| chr1:108579772 | T | TGAGAGAG others(25): Show |
3 | a0001c0001t0001g0084 a0001c0001t0001g0140 a0001c0001t0001g0145 |
3 | HG01169.hp1 HG02559.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.137+19231_137+1923 others(36): Show |
EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 108579772 | ||||||
| chr1:108579772 | T | TGTGAGAG others(5): Show |
9 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0088 others(6): Show |
9 | HG00735.hp2 HG01358.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.137+19208_137+1920 others(16): Show |
EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 108579772 | ||||||
| chr1:108579772 | T | TGTGAGAG others(7): Show |
18 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(15): Show |
21 | HG01070.hp1 HG01074.hp1 HG01361.hp2 others(18): Show |
intron_variant | MODIFIER | c.137+19208_137+1920 others(18): Show |
EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 108579772 | ||||||
| chr1:108579772 | T | TGTGAGAG others(9): Show |
4 | a0001c0001t0001g0003 a0001c0001t0002g0187 a0001c0001t0002g0206 others(1): Show |
5 | HG02622.hp1 NA18953.hp1 NA18956.hp2 others(2): Show |
intron_variant | MODIFIER | c.137+19208_137+1920 others(20): Show |
EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 108579772 | ||||||
| chr1:108579772 | T | TGTGAGAG others(11): Show |
1 | a0001c0001t0001g0091 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.137+19208_137+1920 others(22): Show |
EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 108579772 | ||||||
| chr1:108579772 | T | TGTGAGAG others(13): Show |
2 | a0001c0001t0005g0115 a0001c0001t0005g0121 |
2 | HG02015.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.137+19208_137+1920 others(24): Show |
EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 108579772 | ||||||
| chr1:108579772 | T | TGTGAGAG others(17): Show |
1 | a0001c0001t0001g0092 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.137+19208_137+1920 others(28): Show |
EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 108579772 | ||||||
| chr1:108579772 | T | TGTGAGAG others(19): Show |
6 | a0001c0001t0001g0031 a0001c0001t0001g0093 a0001c0001t0001g0094 others(3): Show |
6 | HG01243.hp1 HG01243.hp2 HG01978.hp2 others(3): Show |
intron_variant | MODIFIER | c.137+19208_137+1920 others(30): Show |
EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 108579772 | ||||||
| chr1:108579772 | T | TGTGAGAG others(21): Show |
4 | a0001c0001t0001g0039 a0001c0001t0001g0095 a0001c0001t0005g0123 others(1): Show |
4 | HG00642.hp2 HG02896.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.137+19208_137+1920 others(32): Show |
EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 108579772 | ||||||
| chr1:108579772 | T | TGTGAGAG others(23): Show |
2 | a0001c0001t0001g0101 a0001c0001t0001g0102 |
2 | HG00642.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.137+19208_137+1920 others(34): Show |
EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 108579772 | ||||||
| chr1:108579772 | T | TGTGAGAG others(25): Show |
1 | a0001c0001t0001g0103 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.137+19208_137+1920 others(36): Show |
EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 108579772 | ||||||
| chr1:108579772 | T | TGTGTGAG others(5): Show |
3 | a0001c0001t0004g0149 a0001c0001t0004g0150 a0001c0001t0004g0152 |
3 | HG02572.hp1 HG02922.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.137+19208_137+1920 others(16): Show |
EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 108579772 | ||||||
| chr1:108579772 | T | TGTGTGAG others(7): Show |
24 | a0001c0001t0002g0005 a0001c0001t0002g0009 a0001c0001t0002g0188 others(21): Show |
26 | HG01069.hp2 HG01071.hp2 HG01884.hp2 others(23): Show |
intron_variant | MODIFIER | c.137+19208_137+1920 others(18): Show |
EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 108579772 | ||||||
| chr1:108579772 | T | TGTGTGAG others(9): Show |
2 | a0001c0001t0002g0189 a0001c0001t0013g0171 |
2 | HG02109.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.137+19208_137+1920 others(20): Show |
EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 108579772 | ||||||
| chr1:108579772 | T | TGTGTGAG others(11): Show |
1 | a0001c0001t0002g0225 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.137+19208_137+1920 others(22): Show |
EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 108579772 | ||||||
| chr1:108579772 | T | TGTGTGAG others(13): Show |
2 | a0001c0001t0002g0229 a0001c0001t0007g0026 |
2 | HG02647.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.137+19208_137+1920 others(24): Show |
EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 108579772 | ||||||
| chr1:108579772 | T | TGTGTGAG others(19): Show |
3 | a0001c0001t0001g0096 a0001c0001t0005g0117 a0001c0001t0005g0124 |
3 | HG02970.hp2 HG03831.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.137+19208_137+1920 others(30): Show |
EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 108579772 | ||||||
| chr1:108579772 | T | TGTGTGAG others(23): Show |
1 | a0001c0001t0001g0040 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.137+19208_137+1920 others(34): Show |
EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 108579772 | ||||||
| chr1:108579772 | T | TGTGTGTG others(5): Show |
3 | a0001c0001t0004g0164 a0001c0001t0004g0165 a0001c0001t0004g0170 |
3 | HG02145.hp2 HG02630.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.137+19208_137+1920 others(16): Show |
EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 108579772 | ||||||
| chr1:108579772 | T | TGTGTGTG others(7): Show |
1 | a0001c0001t0004g0151 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.137+19208_137+1920 others(18): Show |
EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 108579772 | ||||||
| chr1:108579772 | T | TGTGTGTG others(9): Show |
4 | a0001c0001t0002g0226 a0001c0001t0002g0227 a0001c0001t0002g0228 others(1): Show |
4 | HG02004.hp2 HG02886.hp1 NA18964.hp1 others(1): Show |
intron_variant | MODIFIER | c.137+19208_137+1920 others(20): Show |
EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 108579772 | ||||||
| chr1:108579772 | T | TGTGTGTG others(11): Show |
1 | a0001c0001t0002g0177 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.137+19208_137+1920 others(22): Show |
EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 108579772 | ||||||
| chr1:108579772 | T | TGTGTGTG others(13): Show |
1 | a0001c0001t0013g0176 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.137+19208_137+1920 others(24): Show |
EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 108579772 | ||||||
| chr1:108579772 | T | TGTGTGTG others(21): Show |
1 | a0001c0001t0005g0118 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.137+19208_137+1920 others(32): Show |
EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 108579772 | ||||||
| chr1:108579772 | T | TGTGTGTG others(29): Show |
1 | a0001c0001t0001g0104 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.137+19208_137+1920 others(40): Show |
EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 108579772 | ||||||
| chr1:108579772 | T | TGTGTGTG others(7): Show |
1 | a0001c0001t0004g0166 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.137+19208_137+1920 others(18): Show |
EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 108579772 | ||||||
| chr1:108579772 | T | TGTGTGTG others(9): Show |
5 | a0001c0001t0002g0190 a0001c0001t0002g0233 a0001c0001t0004g0153 others(2): Show |
5 | HG02717.hp2 HG03669.hp1 NA19011.hp1 others(2): Show |
intron_variant | MODIFIER | c.137+19208_137+1920 others(20): Show |
EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 108579772 | ||||||
| chr1:108579772 | T | TGTGTGTG others(11): Show |
2 | a0001c0001t0002g0192 a0001c0001t0004g0167 |
2 | HG01496.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.137+19208_137+1920 others(22): Show |
EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 108579772 | ||||||
| chr1:108579772 | T | TGTGTGTG others(11): Show |
1 | a0001c0001t0004g0168 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.137+19208_137+1920 others(22): Show |
EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 108579772 | ||||||
| chr1:108579772 | T | TGTGTGTG others(11): Show |
1 | a0001c0001t0002g0236 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.137+19208_137+1920 others(22): Show |
EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 108579772 | ||||||
| chr1:108579772 | T | TGTGTGTG others(13): Show |
1 | a0001c0001t0004g0169 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.137+19208_137+1920 others(24): Show |
EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 108579772 | ||||||
| chr1:108579772 | TGA | T | 3 | a0001c0001t0003g0247 a0001c0001t0024g0147 a0001c0001t0032g0262 |
3 | NA18522.hp1 NA18968.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.137+19230_137+1923 others(6): Show |
EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 108579772 | ||||||
| chr1:108579774 | A | T | 23 | a0001c0001t0003g0001 a0001c0001t0003g0237 a0001c0001t0003g0238 others(20): Show |
25 | HG00423.hp1 HG02135.hp2 HG02738.hp2 others(22): Show |
intron_variant | MODIFIER | c.137+19209A>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108579774 | |||||||
| chr1:108579776 | A | T | 1 | a0001c0001t0003g0256 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.137+19211A>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108579776 | |||||||
| chr1:108579796 | A | AGAGAGAG others(6): Show |
3 | a0001c0001t0001g0045 a0001c0001t0001g0070 a0001c0001t0001g0125 |
3 | HG02155.hp2 HG04228.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.137+19231_137+1923 others(17): Show |
EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108579796 | |||||||
| chr1:108579796 | A | AGAGAGAG others(18): Show |
1 | a0001c0001t0005g0122 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.137+19231_137+1923 others(29): Show |
EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108579796 | |||||||
| chr1:108579796 | A | AGAGAGAG others(20): Show |
1 | a0001c0001t0009g0023 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.137+19231_137+1923 others(31): Show |
EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108579796 | |||||||
| chr1:108579796 | A | AGAGAGAG others(24): Show |
1 | a0001c0001t0001g0085 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.137+19231_137+1923 others(35): Show |
EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108579796 | |||||||
| chr1:108579811 | C | T | 142 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(139): Show |
143 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(140): Show |
intron_variant | MODIFIER | c.137+19246C>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108579811 | |||||||
| chr1:108579832 | C | T | 7 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0177 others(4): Show |
9 | HG02109.hp2 HG02145.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.137+19267C>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108579832 | |||||||
| chr1:108579845 | T | A | 2 | a0001c0001t0016g0159 a0001c0001t0016g0160 |
2 | HG02258.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.137+19280T>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108579845 | |||||||
| chr1:108579946 | G | T | 9 | a0001c0001t0001g0049 a0001c0001t0001g0063 a0001c0001t0001g0064 others(6): Show |
9 | HG00639.hp2 HG01106.hp1 HG01257.hp2 others(6): Show |
intron_variant | MODIFIER | c.137+19381G>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108579946 | |||||||
| chr1:108579984 | C | A | 1 | a0001c0001t0013g0171 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.137+19419C>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108579984 | |||||||
| chr1:108580036 | A | G | 1 | a0001c0001t0024g0147 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.137+19471A>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108580036 | |||||||
| chr1:108580084 | G | A | 1 | a0001c0001t0005g0124 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.137+19519G>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108580084 | |||||||
| chr1:108580251 | A | G | 1 | a0001c0001t0032g0262 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.137+19686A>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108580251 | |||||||
| chr1:108580284 | A | T | 2 | a0001c0001t0015g0172 a0001c0001t0015g0173 |
2 | HG02647.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.137+19719A>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108580284 | |||||||
| chr1:108580322 | G | A | 1 | a0001c0001t0001g0003 | 2 | NA18953.hp1 NA18956.hp2 |
intron_variant | MODIFIER | c.137+19757G>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108580322 | |||||||
| chr1:108580369 | AACCCT | A | 142 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(139): Show |
143 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(140): Show |
intron_variant | MODIFIER | c.137+19807_137+1981 others(9): Show |
EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 108580369 | ||||||
| chr1:108580424 | C | G | 2 | a0001c0001t0016g0159 a0001c0001t0016g0160 |
2 | HG02258.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.137+19859C>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108580424 | |||||||
| chr1:108580468 | A | G | 1 | a0001c0001t0032g0262 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.137+19903A>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108580468 | |||||||
| chr1:108580596 | G | A | 83 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(80): Show |
88 | HG00408.hp2 HG01069.hp2 HG01070.hp1 others(85): Show |
intron_variant | MODIFIER | c.138-19970G>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108580596 | |||||||
| chr1:108580681 | AAATTCCC others(2): Show |
A | 83 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(80): Show |
88 | HG00408.hp2 HG01069.hp2 HG01070.hp1 others(85): Show |
intron_variant | MODIFIER | c.138-19882_138-1987 others(13): Show |
EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 108580681 | ||||||
| chr1:108580953 | T | C | 1 | a0001c0001t0002g0189 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.138-19613T>C | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108580953 | |||||||
| chr1:108581021 | G | A | 8 | a0001c0001t0002g0005 a0001c0001t0002g0184 a0001c0001t0002g0190 others(5): Show |
9 | HG01069.hp2 HG01071.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.138-19545G>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108581021 | |||||||
| chr1:108581148 | T | C | 2 | a0001c0001t0016g0159 a0001c0001t0016g0160 |
2 | HG02258.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.138-19418T>C | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108581148 | |||||||
| chr1:108581216 | GA | G | 81 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(78): Show |
86 | HG00408.hp2 HG01069.hp2 HG01070.hp1 others(83): Show |
intron_variant | MODIFIER | c.138-19341delA | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 108581216 | ||||||
| chr1:108581266 | A | C | 1 | a0001c0001t0001g0145 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.138-19300A>C | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108581266 | |||||||
| chr1:108581484 | A | G | 7 | a0001c0001t0001g0045 a0001c0001t0001g0059 a0001c0001t0001g0060 others(4): Show |
7 | HG00423.hp2 HG01978.hp1 HG02155.hp2 others(4): Show |
intron_variant | MODIFIER | c.138-19082A>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108581484 | |||||||
| chr1:108581545 | CAG | C | 65 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(62): Show |
70 | HG00408.hp2 HG01069.hp2 HG01070.hp1 others(67): Show |
intron_variant | MODIFIER | c.138-19020_138-1901 others(6): Show |
EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108581545 | |||||||
| chr1:108581570 | G | T | 1 | a0001c0001t0001g0141 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.138-18996G>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108581570 | |||||||
| chr1:108581573 | C | T | 1 | a0001c0001t0001g0046 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.138-18993C>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108581573 | |||||||
| chr1:108581577 | A | C | 1 | a0001c0001t0026g0246 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.138-18989A>C | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108581577 | |||||||
| chr1:108581620 | C | T | 2 | a0001c0001t0010g0002 a0001c0001t0018g0002 |
2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.138-18946C>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108581620 | |||||||
| chr1:108581929 | A | G | 1 | a0001c0001t0001g0069 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.138-18637A>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108581929 | |||||||
| chr1:108581950 | C | G | 5 | a0001c0001t0003g0001 a0001c0001t0003g0247 a0001c0001t0003g0254 others(2): Show |
7 | NA18956.hp1 NA18963.hp2 NA18968.hp1 others(4): Show |
intron_variant | MODIFIER | c.138-18616C>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108581950 | |||||||
| chr1:108581962 | C | G | 81 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(78): Show |
86 | HG00408.hp2 HG01069.hp2 HG01070.hp1 others(83): Show |
intron_variant | MODIFIER | c.138-18604C>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108581962 | |||||||
| chr1:108582004 | C | T | 140 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(137): Show |
141 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(138): Show |
intron_variant | MODIFIER | c.138-18562C>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108582004 | |||||||
| chr1:108582036 | C | A | 2 | a0001c0001t0016g0159 a0001c0001t0016g0160 |
2 | HG02258.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.138-18530C>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108582036 | |||||||
| chr1:108582036 | C | G | 141 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(138): Show |
142 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(139): Show |
intron_variant | MODIFIER | c.138-18530C>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108582036 | |||||||
| chr1:108582067 | A | G | 3 | a0001c0001t0002g0005 a0001c0001t0002g0184 a0001c0001t0028g0185 |
4 | HG01069.hp2 HG01071.hp2 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.138-18499A>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108582067 | |||||||
| chr1:108582374 | G | A | 1 | a0001c0001t0003g0249 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.138-18192G>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108582374 | |||||||
| chr1:108582648 | G | A | 4 | a0001c0001t0004g0166 a0001c0001t0004g0167 a0001c0001t0004g0168 others(1): Show |
4 | HG01891.hp1 HG02258.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.138-17918G>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108582648 | |||||||
| chr1:108582662 | A | AT | 232 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(229): Show |
238 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(235): Show |
intron_variant | MODIFIER | c.138-17898dupT | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 108582662 | ||||||
| chr1:108582798 | G | T | 2 | a0001c0001t0014g0234 a0001c0001t0014g0235 |
2 | HG01884.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.138-17768G>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108582798 | |||||||
| chr1:108582837 | G | A | 81 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(78): Show |
86 | HG00408.hp2 HG01069.hp2 HG01070.hp1 others(83): Show |
intron_variant | MODIFIER | c.138-17729G>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108582837 | |||||||
| chr1:108582955 | T | C | 5 | a0001c0001t0006g0178 a0001c0001t0006g0179 a0001c0001t0006g0180 others(2): Show |
5 | HG02559.hp1 HG02886.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.138-17611T>C | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108582955 | |||||||
| chr1:108582972 | A | AC | 24 | a0001c0001t0002g0005 a0001c0001t0002g0184 a0001c0001t0002g0190 others(21): Show |
25 | HG01069.hp2 HG01071.hp2 HG01884.hp2 others(22): Show |
intron_variant | MODIFIER | c.138-17588dupC | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 108582972 | ||||||
| chr1:108582972 | A | ACC | 56 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(53): Show |
60 | HG00408.hp2 HG01070.hp1 HG01074.hp1 others(57): Show |
intron_variant | MODIFIER | c.138-17589_138-1758 others(6): Show |
EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 108582972 | ||||||
| chr1:108582979 | A | C | 65 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(62): Show |
70 | HG00408.hp2 HG01069.hp2 HG01070.hp1 others(67): Show |
intron_variant | MODIFIER | c.138-17587A>C | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108582979 | |||||||
| chr1:108582985 | A | G | 2 | a0001c0001t0029g0174 a0001c0001t0030g0175 |
2 | HG02630.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.138-17581A>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108582985 | |||||||
| chr1:108583261 | G | T | 7 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0101 others(4): Show |
7 | HG00642.hp1 HG02055.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.138-17305G>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108583261 | |||||||
| chr1:108583290 | G | T | 2 | a0001c0001t0024g0147 a0001c0001t0031g0148 |
2 | NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.138-17276G>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108583290 | |||||||
| chr1:108583297 | A | G | 2 | a0001c0001t0002g0194 a0001c0001t0002g0205 |
2 | HG02155.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.138-17269A>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108583297 | |||||||
| chr1:108583448 | C | CT | 19 | a0001c0001t0004g0149 a0001c0001t0004g0150 a0001c0001t0004g0151 others(16): Show |
19 | HG01891.hp1 HG02145.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.138-17105dupT | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 108583448 | ||||||
| chr1:108583531 | A | G | 81 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(78): Show |
86 | HG00408.hp2 HG01069.hp2 HG01070.hp1 others(83): Show |
intron_variant | MODIFIER | c.138-17035A>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108583531 | |||||||
| chr1:108583598 | T | G | 2 | a0001c0001t0005g0117 a0001c0001t0005g0118 |
2 | NA18952.hp2 NA18960.hp1 |
intron_variant | MODIFIER | c.138-16968T>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108583598 | |||||||
| chr1:108583602 | C | T | 142 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(139): Show |
143 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(140): Show |
intron_variant | MODIFIER | c.138-16964C>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108583602 | |||||||
| chr1:108583777 | G | A | 57 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(54): Show |
61 | HG00408.hp2 HG01070.hp1 HG01074.hp1 others(58): Show |
intron_variant | MODIFIER | c.138-16789G>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108583777 | |||||||
| chr1:108583882 | T | C | 142 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(139): Show |
143 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(140): Show |
intron_variant | MODIFIER | c.138-16684T>C | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108583882 | |||||||
| chr1:108584228 | AACATGAT others(3): Show |
A | 2 | a0001c0001t0024g0147 a0001c0001t0031g0148 |
2 | NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.138-16333_138-1632 others(14): Show |
EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 108584228 | ||||||
| chr1:108584313 | G | C | 2 | a0001c0001t0016g0159 a0001c0001t0016g0160 |
2 | HG02258.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.138-16253G>C | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108584313 | |||||||
| chr1:108584332 | AT | A | 7 | a0001c0001t0004g0149 a0001c0001t0004g0150 a0001c0001t0004g0151 others(4): Show |
7 | HG02572.hp1 HG02717.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.138-16225delT | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 108584332 | ||||||
| chr1:108584506 | T | G | 1 | a0001c0001t0013g0171 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.138-16060T>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108584506 | |||||||
| chr1:108584531 | A | G | 1 | a0001c0001t0025g0161 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.138-16035A>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108584531 | |||||||
| chr1:108584534 | G | A | 2 | a0001c0001t0016g0159 a0001c0001t0016g0160 |
2 | HG02258.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.138-16032G>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108584534 | |||||||
| chr1:108584561 | T | C | 1 | a0001c0001t0013g0176 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.138-16005T>C | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108584561 | |||||||
| chr1:108584744 | A | G | 1 | a0001c0001t0002g0224 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.138-15822A>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108584744 | |||||||
| chr1:108584874 | A | G | 1 | a0001c0001t0001g0015 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.138-15692A>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108584874 | |||||||
| chr1:108585023 | T | C | 81 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(78): Show |
86 | HG00408.hp2 HG01069.hp2 HG01070.hp1 others(83): Show |
intron_variant | MODIFIER | c.138-15543T>C | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108585023 | |||||||
| chr1:108585024 | G | A | 2 | a0001c0001t0004g0154 a0001c0001t0004g0155 |
2 | HG02717.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.138-15542G>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108585024 | |||||||
| chr1:108585381 | G | A | 2 | a0001c0001t0016g0159 a0001c0001t0016g0160 |
2 | HG02258.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.138-15185G>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108585381 | |||||||
| chr1:108585655 | A | G | 1 | a0001c0001t0012g0090 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.138-14911A>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108585655 | |||||||
| chr1:108585852 | C | G | 2 | a0001c0001t0002g0005 a0001c0001t0002g0184 |
3 | HG01069.hp2 HG01071.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.138-14714C>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108585852 | |||||||
| chr1:108585903 | A | C | 1 | a0001c0001t0001g0070 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.138-14663A>C | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108585903 | |||||||
| chr1:108585908 | T | A | 4 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0099 others(1): Show |
4 | HG00735.hp2 HG01256.hp1 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.138-14658T>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108585908 | |||||||
| chr1:108585944 | T | C | 81 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(78): Show |
86 | HG00408.hp2 HG01069.hp2 HG01070.hp1 others(83): Show |
intron_variant | MODIFIER | c.138-14622T>C | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108585944 | |||||||
| chr1:108586168 | C | G | 57 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(54): Show |
61 | HG00408.hp2 HG01070.hp1 HG01074.hp1 others(58): Show |
intron_variant | MODIFIER | c.138-14398C>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108586168 | |||||||
| chr1:108586282 | A | G | 81 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(78): Show |
86 | HG00408.hp2 HG01069.hp2 HG01070.hp1 others(83): Show |
intron_variant | MODIFIER | c.138-14284A>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108586282 | |||||||
| chr1:108586314 | G | GGT | 11 | a0001c0001t0002g0204 a0001c0001t0002g0220 a0001c0001t0002g0221 others(8): Show |
13 | HG01928.hp1 HG02055.hp1 NA18940.hp1 others(10): Show |
intron_variant | MODIFIER | c.138-14213_138-1421 others(6): Show |
EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 108586314 | ||||||
| chr1:108586314 | GGT | G | 44 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(41): Show |
48 | HG00408.hp2 HG00423.hp1 HG01069.hp2 others(45): Show |
intron_variant | MODIFIER | c.138-14213_138-1421 others(6): Show |
EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 108586314 | ||||||
| chr1:108586314 | GGTGT | G | 16 | a0001c0001t0002g0233 a0001c0001t0004g0149 a0001c0001t0004g0150 others(13): Show |
16 | HG01891.hp1 HG02145.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.138-14215_138-1421 others(8): Show |
EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 108586314 | ||||||
| chr1:108586314 | GGTGTGT | G | 3 | a0001c0001t0016g0159 a0001c0001t0016g0160 a0001c0001t0029g0174 |
3 | HG02258.hp2 HG02630.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.138-14217_138-1421 others(10): Show |
EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 108586314 | ||||||
| chr1:108586314 | GGTGTGTG others(3): Show |
G | 17 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0048 others(14): Show |
17 | HG01243.hp1 HG01243.hp2 HG02015.hp1 others(14): Show |
intron_variant | MODIFIER | c.138-14221_138-1421 others(14): Show |
EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 108586314 | ||||||
| chr1:108586314 | GGTGTGTG others(5): Show |
G | 129 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(126): Show |
130 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(127): Show |
intron_variant | MODIFIER | c.138-14223_138-1421 others(16): Show |
EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 108586314 | ||||||
| chr1:108586754 | C | T | 1 | a0001c0001t0003g0253 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.138-13812C>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108586754 | |||||||
| chr1:108587444 | C | T | 1 | a0001c0001t0001g0068 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.138-13122C>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108587444 | |||||||
| chr1:108587501 | T | A | 1 | a0001c0001t0025g0161 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.138-13065T>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108587501 | |||||||
| chr1:108587539 | T | C | 2 | a0001c0001t0016g0159 a0001c0001t0016g0160 |
2 | HG02258.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.138-13027T>C | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108587539 | |||||||
| chr1:108587974 | C | A | 23 | a0001c0001t0003g0001 a0001c0001t0003g0237 a0001c0001t0003g0238 others(20): Show |
25 | HG00423.hp1 HG02135.hp2 HG03669.hp2 others(22): Show |
intron_variant | MODIFIER | c.138-12592C>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108587974 | |||||||
| chr1:108587975 | G | A | 81 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(78): Show |
86 | HG00408.hp2 HG01069.hp2 HG01070.hp1 others(83): Show |
intron_variant | MODIFIER | c.138-12591G>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108587975 | |||||||
| chr1:108588068 | A | G | 1 | a0001c0001t0031g0148 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.138-12498A>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108588068 | |||||||
| chr1:108588163 | A | G | 2 | a0001c0001t0004g0162 a0001c0001t0004g0163 |
2 | HG02809.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.138-12403A>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108588163 | |||||||
| chr1:108588401 | A | C | 90 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0015 others(87): Show |
91 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(88): Show |
intron_variant | MODIFIER | c.138-12165A>C | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108588401 | |||||||
| chr1:108588635 | T | C | 1 | a0001c0001t0013g0176 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.138-11931T>C | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108588635 | |||||||
| chr1:108588728 | C | CT | 81 | a0001c0001t0001g0048 a0001c0001t0002g0005 a0001c0001t0002g0006 others(78): Show |
86 | HG00408.hp2 HG01069.hp2 HG01070.hp1 others(83): Show |
intron_variant | MODIFIER | c.138-11823dupT | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 108588728 | ||||||
| chr1:108588947 | A | G | 1 | a0001c0001t0001g0058 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.138-11619A>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108588947 | |||||||
| chr1:108588976 | T | A | 85 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(82): Show |
90 | HG00408.hp2 HG01069.hp2 HG01070.hp1 others(87): Show |
intron_variant | MODIFIER | c.138-11590T>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108588976 | |||||||
| chr1:108589147 | C | T | 1 | a0001c0001t0002g0184 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.138-11419C>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108589147 | |||||||
| chr1:108589363 | C | G | 2 | a0001c0001t0005g0117 a0001c0001t0005g0118 |
2 | NA18952.hp2 NA18960.hp1 |
intron_variant | MODIFIER | c.138-11203C>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108589363 | |||||||
| chr1:108589417 | T | C | 81 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(78): Show |
86 | HG00408.hp2 HG01069.hp2 HG01070.hp1 others(83): Show |
intron_variant | MODIFIER | c.138-11149T>C | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108589417 | |||||||
| chr1:108589585 | G | A | 1 | a0001c0001t0013g0176 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.138-10981G>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108589585 | |||||||
| chr1:108589615 | G | A | 1 | a0001c0001t0002g0210 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.138-10951G>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108589615 | |||||||
| chr1:108589783 | C | CT | 74 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0015 others(71): Show |
78 | HG00408.hp2 HG00735.hp2 HG00738.hp1 others(75): Show |
intron_variant | MODIFIER | c.138-10758dupT | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 108589783 | ||||||
| chr1:108589783 | C | CTT | 39 | a0001c0001t0002g0009 a0001c0001t0002g0191 a0001c0001t0002g0192 others(36): Show |
40 | HG01361.hp2 HG01496.hp2 HG01891.hp1 others(37): Show |
intron_variant | MODIFIER | c.138-10759_138-1075 others(6): Show |
EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 108589783 | ||||||
| chr1:108589783 | C | CTTT | 7 | a0001c0001t0002g0218 a0001c0001t0002g0219 a0001c0001t0002g0223 others(4): Show |
7 | HG02572.hp1 HG02630.hp2 HG03579.hp2 others(4): Show |
intron_variant | MODIFIER | c.138-10760_138-1075 others(7): Show |
EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 108589783 | ||||||
| chr1:108589783 | CT | C | 6 | a0001c0001t0001g0040 a0001c0001t0001g0088 a0001c0001t0001g0099 others(3): Show |
6 | HG01256.hp1 HG02897.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.138-10758delT | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 108589783 | ||||||
| chr1:108589946 | A | G | 2 | a0001c0001t0001g0071 a0001c0001t0001g0126 |
2 | NA18964.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.138-10620A>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108589946 | |||||||
| chr1:108590110 | C | T | 1 | a0001c0001t0002g0211 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.138-10456C>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108590110 | |||||||
| chr1:108590250 | A | G | 1 | a0001c0001t0001g0082 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.138-10316A>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108590250 | |||||||
| chr1:108590635 | G | A | 2 | a0001c0001t0016g0159 a0001c0001t0016g0160 |
2 | HG02258.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.138-9931G>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108590635 | |||||||
| chr1:108590699 | A | G | 1 | a0001c0001t0001g0012 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.138-9867A>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108590699 | |||||||
| chr1:108590713 | G | A | 5 | a0001c0001t0007g0018 a0001c0001t0007g0019 a0001c0001t0007g0020 others(2): Show |
5 | HG02451.hp2 HG02647.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.138-9853G>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108590713 | |||||||
| chr1:108591069 | T | C | 85 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(82): Show |
90 | HG00408.hp2 HG01069.hp2 HG01070.hp1 others(87): Show |
intron_variant | MODIFIER | c.138-9497T>C | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108591069 | |||||||
| chr1:108591156 | A | G | 1 | a0001c0001t0002g0225 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.138-9410A>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108591156 | |||||||
| chr1:108591217 | A | G | 26 | a0001c0001t0001g0010 a0001c0001t0001g0033 a0001c0001t0001g0034 others(23): Show |
26 | HG00642.hp2 HG00738.hp2 HG01106.hp2 others(23): Show |
intron_variant | MODIFIER | c.138-9349A>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108591217 | |||||||
| chr1:108591402 | A | C | 1 | a0001c0001t0013g0176 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.138-9164A>C | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108591402 | |||||||
| chr1:108591462 | C | T | 2 | a0001c0001t0015g0172 a0001c0001t0015g0173 |
2 | HG02647.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.138-9104C>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108591462 | |||||||
| chr1:108591573 | C | A | 1 | a0001c0001t0002g0199 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.138-8993C>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108591573 | |||||||
| chr1:108591697 | G | A | 3 | a0001c0001t0015g0172 a0001c0001t0015g0173 a0001c0001t0032g0262 |
3 | HG02647.hp1 HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.138-8869G>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108591697 | |||||||
| chr1:108591797 | G | A | 3 | a0001c0001t0015g0172 a0001c0001t0015g0173 a0001c0001t0032g0262 |
3 | HG02647.hp1 HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.138-8769G>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108591797 | |||||||
| chr1:108592116 | G | A | 1 | a0001c0001t0001g0129 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.138-8450G>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108592116 | |||||||
| chr1:108592159 | A | G | 1 | a0001c0001t0001g0044 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.138-8407A>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108592159 | |||||||
| chr1:108592675 | G | A | 1 | a0001c0001t0001g0059 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.138-7891G>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108592675 | |||||||
| chr1:108592945 | T | C | 85 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(82): Show |
90 | HG00408.hp2 HG01069.hp2 HG01070.hp1 others(87): Show |
intron_variant | MODIFIER | c.138-7621T>C | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108592945 | |||||||
| chr1:108592983 | C | A | 2 | a0001c0001t0004g0162 a0001c0001t0004g0163 |
2 | HG02809.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.138-7583C>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108592983 | |||||||
| chr1:108593134 | A | G | 258 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(255): Show |
266 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(263): Show |
intron_variant | MODIFIER | c.138-7432A>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108593134 | |||||||
| chr1:108593247 | G | T | 25 | a0001c0001t0001g0010 a0001c0001t0001g0033 a0001c0001t0001g0034 others(22): Show |
25 | HG00642.hp2 HG00738.hp2 HG01106.hp2 others(22): Show |
intron_variant | MODIFIER | c.138-7319G>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108593247 | |||||||
| chr1:108593414 | T | C | 85 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(82): Show |
90 | HG00408.hp2 HG01069.hp2 HG01070.hp1 others(87): Show |
intron_variant | MODIFIER | c.138-7152T>C | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108593414 | |||||||
| chr1:108593541 | G | A | 1 | a0001c0001t0002g0226 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.138-7025G>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108593541 | |||||||
| chr1:108593564 | G | C | 9 | a0001c0001t0001g0049 a0001c0001t0001g0063 a0001c0001t0001g0064 others(6): Show |
9 | HG00639.hp2 HG01106.hp1 HG01257.hp2 others(6): Show |
intron_variant | MODIFIER | c.138-7002G>C | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108593564 | |||||||
| chr1:108593608 | G | A | 4 | a0001c0001t0004g0149 a0001c0001t0004g0150 a0001c0001t0004g0151 others(1): Show |
4 | HG02572.hp1 HG02809.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.138-6958G>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108593608 | |||||||
| chr1:108593866 | C | T | 2 | a0001c0001t0029g0174 a0001c0001t0030g0175 |
2 | HG02630.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.138-6700C>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108593866 | |||||||
| chr1:108593987 | T | C | 85 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(82): Show |
90 | HG00408.hp2 HG01069.hp2 HG01070.hp1 others(87): Show |
intron_variant | MODIFIER | c.138-6579T>C | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108593987 | |||||||
| chr1:108594049 | C | G | 1 | a0001c0001t0003g0243 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.138-6517C>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108594049 | |||||||
| chr1:108594242 | C | T | 2 | a0001c0001t0016g0159 a0001c0001t0016g0160 |
2 | HG02258.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.138-6324C>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108594242 | |||||||
| chr1:108594285 | G | C | 1 | a0001c0001t0001g0125 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.138-6281G>C | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108594285 | |||||||
| chr1:108594291 | A | G | 2 | a0001c0001t0029g0174 a0001c0001t0030g0175 |
2 | HG02630.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.138-6275A>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108594291 | |||||||
| chr1:108594343 | G | A | 4 | a0001c0001t0016g0159 a0001c0001t0016g0160 a0001c0001t0029g0174 others(1): Show |
4 | HG02258.hp2 HG02630.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.138-6223G>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108594343 | |||||||
| chr1:108594618 | T | A | 2 | a0001c0001t0029g0174 a0001c0001t0030g0175 |
2 | HG02630.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.138-5948T>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108594618 | |||||||
| chr1:108594876 | A | C | 2 | a0001c0001t0016g0159 a0001c0001t0016g0160 |
2 | HG02258.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.138-5690A>C | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108594876 | |||||||
| chr1:108595224 | A | G | 1 | a0001c0001t0013g0176 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.138-5342A>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108595224 | |||||||
| chr1:108595531 | A | G | 141 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(138): Show |
142 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(139): Show |
intron_variant | MODIFIER | c.138-5035A>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108595531 | |||||||
| chr1:108595814 | A | T | 1 | a0001c0001t0001g0133 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.138-4752A>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108595814 | |||||||
| chr1:108595891 | GTTTCT | G | 5 | a0001c0001t0006g0178 a0001c0001t0006g0179 a0001c0001t0006g0180 others(2): Show |
5 | HG02559.hp1 HG02886.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.138-4671_138-4667d others(7): Show |
EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 108595891 | ||||||
| chr1:108595928 | C | T | 5 | a0001c0001t0006g0178 a0001c0001t0006g0179 a0001c0001t0006g0180 others(2): Show |
5 | HG02559.hp1 HG02886.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.138-4638C>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108595928 | |||||||
| chr1:108596045 | C | T | 77 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(74): Show |
82 | HG00408.hp2 HG01069.hp2 HG01070.hp1 others(79): Show |
intron_variant | MODIFIER | c.138-4521C>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108596045 | |||||||
| chr1:108596046 | A | G | 77 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(74): Show |
82 | HG00408.hp2 HG01069.hp2 HG01070.hp1 others(79): Show |
intron_variant | MODIFIER | c.138-4520A>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108596046 | |||||||
| chr1:108596176 | G | GT | 8 | a0001c0001t0006g0178 a0001c0001t0006g0179 a0001c0001t0006g0180 others(5): Show |
8 | HG02559.hp1 HG02630.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.138-4378dupT | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 108596176 | ||||||
| chr1:108596202 | A | T | 1 | a0001c0001t0001g0055 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.138-4364A>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108596202 | |||||||
| chr1:108596220 | T | C | 1 | a0001c0001t0030g0175 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.138-4346T>C | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108596220 | |||||||
| chr1:108596237 | T | G | 1 | a0001c0001t0030g0175 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.138-4329T>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108596237 | |||||||
| chr1:108596300 | T | C | 2 | a0001c0001t0004g0154 a0001c0001t0004g0155 |
2 | HG02717.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.138-4266T>C | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108596300 | |||||||
| chr1:108596429 | T | C | 258 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(255): Show |
266 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(263): Show |
intron_variant | MODIFIER | c.138-4137T>C | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108596429 | |||||||
| chr1:108596473 | G | A | 77 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(74): Show |
82 | HG00408.hp2 HG01069.hp2 HG01070.hp1 others(79): Show |
intron_variant | MODIFIER | c.138-4093G>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108596473 | |||||||
| chr1:108596521 | G | C | 230 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(227): Show |
236 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(233): Show |
intron_variant | MODIFIER | c.138-4045G>C | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108596521 | |||||||
| chr1:108596623 | T | A | 77 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(74): Show |
82 | HG00408.hp2 HG01069.hp2 HG01070.hp1 others(79): Show |
intron_variant | MODIFIER | c.138-3943T>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108596623 | |||||||
| chr1:108596671 | A | G | 1 | a0001c0001t0012g0057 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.138-3895A>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108596671 | |||||||
| chr1:108596717 | G | A | 4 | a0001c0001t0004g0149 a0001c0001t0004g0150 a0001c0001t0004g0151 others(1): Show |
4 | HG02572.hp1 HG02809.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.138-3849G>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108596717 | |||||||
| chr1:108596737 | G | GTT | 5 | a0001c0001t0006g0178 a0001c0001t0006g0179 a0001c0001t0006g0180 others(2): Show |
5 | HG02559.hp1 HG02886.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.138-3823_138-3822d others(4): Show |
EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 108596737 | ||||||
| chr1:108596745 | G | T | 5 | a0001c0001t0006g0178 a0001c0001t0006g0179 a0001c0001t0006g0180 others(2): Show |
5 | HG02559.hp1 HG02886.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.138-3821G>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108596745 | |||||||
| chr1:108596833 | G | T | 1 | a0001c0001t0001g0058 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.138-3733G>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108596833 | |||||||
| chr1:108597007 | A | G | 24 | a0001c0001t0003g0001 a0001c0001t0003g0237 a0001c0001t0003g0238 others(21): Show |
26 | HG00423.hp1 HG02135.hp2 HG03669.hp2 others(23): Show |
intron_variant | MODIFIER | c.138-3559A>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108597007 | |||||||
| chr1:108597296 | T | C | 1 | a0001c0001t0001g0079 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.138-3270T>C | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108597296 | |||||||
| chr1:108597523 | A | G | 9 | a0001c0001t0004g0162 a0001c0001t0004g0163 a0001c0001t0004g0164 others(6): Show |
9 | HG01891.hp1 HG02145.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.138-3043A>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108597523 | |||||||
| chr1:108597544 | C | G | 3 | a0001c0001t0004g0162 a0001c0001t0004g0163 a0001c0001t0004g0164 |
3 | HG02630.hp2 HG02809.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.138-3022C>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108597544 | |||||||
| chr1:108597654 | T | C | 1 | a0001c0001t0024g0147 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.138-2912T>C | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108597654 | |||||||
| chr1:108597660 | GTC | G | 5 | a0001c0001t0006g0178 a0001c0001t0006g0179 a0001c0001t0006g0180 others(2): Show |
5 | HG02559.hp1 HG02886.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.138-2904_138-2903d others(4): Show |
EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 108597660 | ||||||
| chr1:108597801 | A | T | 144 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(141): Show |
145 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(142): Show |
intron_variant | MODIFIER | c.138-2765A>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108597801 | |||||||
| chr1:108597854 | T | A | 1 | a0001c0001t0001g0047 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.138-2712T>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108597854 | |||||||
| chr1:108597902 | A | T | 3 | a0001c0001t0015g0172 a0001c0001t0015g0173 a0001c0001t0032g0262 |
3 | HG02647.hp1 HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.138-2664A>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108597902 | |||||||
| chr1:108597905 | C | T | 16 | a0001c0001t0004g0149 a0001c0001t0004g0150 a0001c0001t0004g0151 others(13): Show |
16 | HG01891.hp1 HG02145.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.138-2661C>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108597905 | |||||||
| chr1:108597952 | A | G | 2 | a0001c0001t0002g0005 a0001c0001t0002g0184 |
3 | HG01069.hp2 HG01071.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.138-2614A>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108597952 | |||||||
| chr1:108598047 | C | A | 5 | a0001c0001t0006g0178 a0001c0001t0006g0179 a0001c0001t0006g0180 others(2): Show |
5 | HG02559.hp1 HG02886.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.138-2519C>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108598047 | |||||||
| chr1:108598060 | C | A | 229 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(226): Show |
235 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(232): Show |
intron_variant | MODIFIER | c.138-2506C>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108598060 | |||||||
| chr1:108598078 | TAG | T | 5 | a0001c0001t0006g0178 a0001c0001t0006g0179 a0001c0001t0006g0180 others(2): Show |
5 | HG02559.hp1 HG02886.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.138-2487_138-2486d others(4): Show |
EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108598078 | |||||||
| chr1:108598242 | G | A | 1 | a0001c0001t0032g0262 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.138-2324G>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108598242 | |||||||
| chr1:108598292 | C | G | 1 | a0001c0001t0032g0262 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.138-2274C>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108598292 | |||||||
| chr1:108598312 | C | T | 1 | a0001c0001t0001g0012 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.138-2254C>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108598312 | |||||||
| chr1:108598334 | C | CA | 6 | a0001c0001t0003g0238 a0001c0001t0003g0239 a0001c0001t0003g0243 others(3): Show |
6 | NA18944.hp1 NA18963.hp2 NA18972.hp1 others(3): Show |
intron_variant | MODIFIER | c.138-2208dupA | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 108598334 | ||||||
| chr1:108598334 | CA | C | 25 | a0001c0001t0001g0022 a0001c0001t0001g0030 a0001c0001t0001g0032 others(22): Show |
25 | HG00408.hp1 HG00639.hp1 HG01169.hp2 others(22): Show |
intron_variant | MODIFIER | c.138-2208delA | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 108598334 | ||||||
| chr1:108598334 | CAA | C | 124 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(121): Show |
125 | HG00423.hp2 HG00639.hp2 HG00642.hp1 others(122): Show |
intron_variant | MODIFIER | c.138-2209_138-2208d others(4): Show |
EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 108598334 | ||||||
| chr1:108598334 | CAAAAAAA | C | 5 | a0001c0001t0002g0006 a0001c0001t0002g0195 a0001c0001t0002g0214 others(2): Show |
6 | HG02145.hp1 HG02145.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.138-2214_138-2208d others(9): Show |
EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 108598334 | ||||||
| chr1:108598334 | CAAAAAAA others(1): Show |
C | 73 | a0001c0001t0002g0005 a0001c0001t0002g0007 a0001c0001t0002g0008 others(70): Show |
77 | HG00408.hp2 HG01069.hp2 HG01070.hp1 others(74): Show |
intron_variant | MODIFIER | c.138-2215_138-2208d others(10): Show |
EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 108598334 | ||||||
| chr1:108598355 | A | G | 2 | a0001c0001t0024g0147 a0001c0001t0031g0148 |
2 | NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.138-2211A>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108598355 | |||||||
| chr1:108598364 | A | AT | 84 | a0001c0001t0001g0011 a0001c0001t0002g0005 a0001c0001t0002g0006 others(81): Show |
89 | HG00408.hp2 HG01069.hp2 HG01070.hp1 others(86): Show |
intron_variant | MODIFIER | c.138-2192dupT | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 108598364 | ||||||
| chr1:108598472 | G | A | 2 | a0001c0001t0002g0005 a0001c0001t0002g0184 |
3 | HG01069.hp2 HG01071.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.138-2094G>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108598472 | |||||||
| chr1:108598502 | G | A | 7 | a0001c0001t0004g0149 a0001c0001t0004g0150 a0001c0001t0004g0151 others(4): Show |
7 | HG02572.hp1 HG02717.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.138-2064G>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108598502 | |||||||
| chr1:108598860 | G | C | 1 | a0001c0001t0006g0158 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.138-1706G>C | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108598860 | |||||||
| chr1:108598968 | C | G | 138 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(135): Show |
139 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(136): Show |
intron_variant | MODIFIER | c.138-1598C>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108598968 | |||||||
| chr1:108598982 | A | T | 2 | a0001c0001t0015g0172 a0001c0001t0015g0173 |
2 | HG02647.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.138-1584A>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108598982 | |||||||
| chr1:108599179 | C | A | 7 | a0001c0001t0001g0072 a0001c0001t0002g0006 a0001c0001t0002g0007 others(4): Show |
9 | HG01884.hp1 HG02145.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.138-1387C>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108599179 | |||||||
| chr1:108599179 | C | CA | 6 | a0001c0001t0001g0089 a0001c0001t0001g0105 a0001c0001t0001g0106 others(3): Show |
6 | NA18960.hp1 NA18960.hp2 NA18963.hp2 others(3): Show |
intron_variant | MODIFIER | c.138-1377dupA | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 108599179 | ||||||
| chr1:108599331 | G | A | 1 | a0001c0001t0001g0063 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.138-1235G>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108599331 | |||||||
| chr1:108599336 | T | C | 221 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(218): Show |
227 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(224): Show |
intron_variant | MODIFIER | c.138-1230T>C | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108599336 | |||||||
| chr1:108599784 | G | T | 77 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(74): Show |
82 | HG00408.hp2 HG01069.hp2 HG01070.hp1 others(79): Show |
intron_variant | MODIFIER | c.138-782G>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108599784 | |||||||
| chr1:108599854 | T | C | 1 | a0001c0001t0002g0233 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.138-712T>C | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108599854 | |||||||
| chr1:108599865 | G | A | 1 | a0001c0001t0027g0183 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.138-701G>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108599865 | |||||||
| chr1:108599886 | A | G | 229 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(226): Show |
235 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(232): Show |
intron_variant | MODIFIER | c.138-680A>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108599886 | |||||||
| chr1:108600316 | C | G | 1 | a0001c0001t0013g0176 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.138-250C>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108600316 | |||||||
| chr1:108600371 | A | T | 231 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(228): Show |
237 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(234): Show |
intron_variant | MODIFIER | c.138-195A>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108600371 | |||||||
| chr1:108600471 | C | T | 6 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(3): Show |
6 | HG00738.hp2 HG01169.hp2 HG01975.hp1 others(3): Show |
intron_variant | MODIFIER | c.138-95C>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108600471 | |||||||
| chr1:108600497 | G | T | 1 | a0001c0001t0002g0219 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.138-69G>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 1/10 | chr1 | 108600497 | |||||||
| chr1:108600738 | G | A | 1 | a0001c0001t0023g0132 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.258+52G>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 2/10 | chr1 | 108600738 | |||||||
| chr1:108600750 | T | C | 5 | a0001c0001t0006g0178 a0001c0001t0006g0179 a0001c0001t0006g0180 others(2): Show |
5 | HG02559.hp1 HG02886.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.258+64T>C | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 2/10 | chr1 | 108600750 | |||||||
| chr1:108600835 | A | G | 77 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(74): Show |
82 | HG00408.hp2 HG01069.hp2 HG01070.hp1 others(79): Show |
intron_variant | MODIFIER | c.258+149A>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 2/10 | chr1 | 108600835 | |||||||
| chr1:108601245 | A | G | 77 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(74): Show |
82 | HG00408.hp2 HG01069.hp2 HG01070.hp1 others(79): Show |
intron_variant | MODIFIER | c.258+559A>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 2/10 | chr1 | 108601245 | |||||||
| chr1:108601263 | TGTGTGTG others(17): Show |
T | 1 | a0001c0001t0001g0050 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.258+593_258+616del others(24): Show |
EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 108601263 | ||||||
| chr1:108601378 | AAG | A | 2 | a0001c0001t0001g0039 a0001c0001t0001g0040 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.258+695_258+696del others(2): Show |
EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 108601378 | ||||||
| chr1:108601437 | C | T | 1 | a0001c0001t0002g0220 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.258+751C>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 2/10 | chr1 | 108601437 | |||||||
| chr1:108601475 | A | C | 1 | a0001c0001t0013g0176 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.258+789A>C | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 2/10 | chr1 | 108601475 | |||||||
| chr1:108601558 | T | A | 61 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(58): Show |
66 | HG00408.hp2 HG01069.hp2 HG01070.hp1 others(63): Show |
intron_variant | MODIFIER | c.258+872T>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 2/10 | chr1 | 108601558 | |||||||
| chr1:108601558 | T | G | 3 | a0001c0001t0001g0010 a0001c0001t0001g0074 a0001c0001t0001g0081 |
3 | HG01106.hp2 HG01256.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.258+872T>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 2/10 | chr1 | 108601558 | |||||||
| chr1:108601598 | G | A | 1 | a0001c0001t0001g0126 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.258+912G>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 2/10 | chr1 | 108601598 | |||||||
| chr1:108601678 | A | C | 258 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(255): Show |
266 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(263): Show |
intron_variant | MODIFIER | c.258+992A>C | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 2/10 | chr1 | 108601678 | |||||||
| chr1:108601732 | C | T | 2 | a0001c0001t0029g0174 a0001c0001t0030g0175 |
2 | HG02630.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.258+1046C>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 2/10 | chr1 | 108601732 | |||||||
| chr1:108601916 | G | T | 1 | a0001c0001t0001g0070 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.258+1230G>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 2/10 | chr1 | 108601916 | |||||||
| chr1:108601960 | A | T | 1 | a0001c0001t0027g0183 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.258+1274A>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 2/10 | chr1 | 108601960 | |||||||
| chr1:108602300 | T | A | 1 | a0001c0001t0001g0107 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.258+1614T>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 2/10 | chr1 | 108602300 | |||||||
| chr1:108602873 | CA | C | 221 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(218): Show |
226 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(223): Show |
intron_variant | MODIFIER | c.258+2198delA | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 108602873 | ||||||
| chr1:108602955 | C | CG | 77 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(74): Show |
82 | HG00408.hp2 HG01069.hp2 HG01070.hp1 others(79): Show |
intron_variant | MODIFIER | c.258+2274dupG | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 108602955 | ||||||
| chr1:108603198 | G | A | 1 | a0001c0001t0001g0037 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.258+2512G>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 2/10 | chr1 | 108603198 | |||||||
| chr1:108603332 | T | C | 140 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(137): Show |
141 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(138): Show |
intron_variant | MODIFIER | c.258+2646T>C | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 2/10 | chr1 | 108603332 | |||||||
| chr1:108603432 | A | T | 23 | a0001c0001t0003g0001 a0001c0001t0003g0237 a0001c0001t0003g0238 others(20): Show |
25 | HG00423.hp1 HG02135.hp2 HG03669.hp2 others(22): Show |
intron_variant | MODIFIER | c.258+2746A>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 2/10 | chr1 | 108603432 | |||||||
| chr1:108603459 | C | CTG | 222 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(219): Show |
228 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(225): Show |
intron_variant | MODIFIER | c.259-2764_259-2763i others(4): Show |
EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 2/10 | chr1 | 108603459 | |||||||
| chr1:108603600 | C | T | 8 | a0001c0001t0002g0005 a0001c0001t0002g0184 a0001c0001t0002g0190 others(5): Show |
9 | HG01069.hp2 HG01071.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.259-2623C>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 2/10 | chr1 | 108603600 | |||||||
| chr1:108603938 | T | A | 1 | a0001c0001t0002g0196 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.259-2285T>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 2/10 | chr1 | 108603938 | |||||||
| chr1:108603967 | A | G | 2 | a0001c0001t0009g0021 a0001c0001t0009g0023 |
2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.259-2256A>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 2/10 | chr1 | 108603967 | |||||||
| chr1:108604167 | G | A | 1 | a0001c0001t0003g0257 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.259-2056G>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 2/10 | chr1 | 108604167 | |||||||
| chr1:108604208 | C | T | 6 | a0001c0001t0003g0250 a0001c0001t0003g0251 a0001c0001t0003g0256 others(3): Show |
6 | NA18957.hp1 NA18972.hp1 NA18984.hp2 others(3): Show |
intron_variant | MODIFIER | c.259-2015C>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 2/10 | chr1 | 108604208 | |||||||
| chr1:108604211 | A | C | 1 | a0001c0001t0001g0105 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.259-2012A>C | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 2/10 | chr1 | 108604211 | |||||||
| chr1:108604218 | C | G | 5 | a0001c0001t0006g0178 a0001c0001t0006g0179 a0001c0001t0006g0180 others(2): Show |
5 | HG02559.hp1 HG02886.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.259-2005C>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 2/10 | chr1 | 108604218 | |||||||
| chr1:108604290 | A | T | 5 | a0001c0001t0006g0178 a0001c0001t0006g0179 a0001c0001t0006g0180 others(2): Show |
5 | HG02559.hp1 HG02886.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.259-1933A>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 2/10 | chr1 | 108604290 | |||||||
| chr1:108604690 | G | A | 1 | a0001c0001t0001g0071 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.259-1533G>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 2/10 | chr1 | 108604690 | |||||||
| chr1:108604865 | C | CA | 80 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0022 others(77): Show |
85 | HG00408.hp2 HG00735.hp1 HG00735.hp2 others(82): Show |
intron_variant | MODIFIER | c.259-1342dupA | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 108604865 | ||||||
| chr1:108604987 | G | A | 2 | a0001c0001t0001g0050 a0001c0001t0020g0051 |
2 | HG01943.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.259-1236G>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 2/10 | chr1 | 108604987 | |||||||
| chr1:108605099 | T | C | 2 | a0001c0001t0024g0147 a0001c0001t0031g0148 |
2 | NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.259-1124T>C | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 2/10 | chr1 | 108605099 | |||||||
| chr1:108606063 | G | A | 23 | a0001c0001t0003g0001 a0001c0001t0003g0237 a0001c0001t0003g0238 others(20): Show |
25 | HG00423.hp1 HG02135.hp2 HG03669.hp2 others(22): Show |
intron_variant | MODIFIER | c.259-160G>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 2/10 | chr1 | 108606063 | |||||||
| chr1:108606103 | A | G | 4 | a0001c0001t0001g0107 a0001c0001t0001g0109 a0001c0001t0001g0110 others(1): Show |
4 | NA18947.hp2 NA19068.hp2 NA19075.hp1 others(1): Show |
intron_variant | MODIFIER | c.259-120A>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 2/10 | chr1 | 108606103 | |||||||
| chr1:108606366 | T | A | 3 | a0001c0001t0015g0172 a0001c0001t0015g0173 a0001c0001t0032g0262 |
3 | HG02647.hp1 HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.288+114T>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 3/10 | chr1 | 108606366 | |||||||
| chr1:108606815 | T | C | 1 | a0001c0001t0001g0101 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.288+563T>C | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 3/10 | chr1 | 108606815 | |||||||
| chr1:108606902 | A | G | 1 | a0001c0001t0031g0148 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.288+650A>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 3/10 | chr1 | 108606902 | |||||||
| chr1:108606941 | G | A | 4 | a0001c0001t0004g0166 a0001c0001t0004g0167 a0001c0001t0004g0168 others(1): Show |
4 | HG01891.hp1 HG02258.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.288+689G>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 3/10 | chr1 | 108606941 | |||||||
| chr1:108606943 | G | A | 228 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(225): Show |
234 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(231): Show |
intron_variant | MODIFIER | c.288+691G>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 3/10 | chr1 | 108606943 | |||||||
| chr1:108607217 | G | C | 1 | a0001c0001t0026g0246 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.288+965G>C | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 3/10 | chr1 | 108607217 | |||||||
| chr1:108607247 | G | A | 1 | a0001c0001t0002g0097 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.288+995G>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 3/10 | chr1 | 108607247 | |||||||
| chr1:108607357 | C | T | 2 | a0001c0001t0029g0174 a0001c0001t0030g0175 |
2 | HG02630.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.288+1105C>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 3/10 | chr1 | 108607357 | |||||||
| chr1:108607360 | A | G | 1 | a0001c0001t0004g0155 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.288+1108A>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 3/10 | chr1 | 108607360 | |||||||
| chr1:108607560 | A | C | 1 | a0001c0001t0013g0176 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.288+1308A>C | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 3/10 | chr1 | 108607560 | |||||||
| chr1:108607803 | T | C | 77 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(74): Show |
82 | HG00408.hp2 HG01069.hp2 HG01070.hp1 others(79): Show |
intron_variant | MODIFIER | c.288+1551T>C | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 3/10 | chr1 | 108607803 | |||||||
| chr1:108607818 | G | A | 1 | a0001c0001t0013g0176 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.288+1566G>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 3/10 | chr1 | 108607818 | |||||||
| chr1:108608027 | G | A | 77 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(74): Show |
82 | HG00408.hp2 HG01069.hp2 HG01070.hp1 others(79): Show |
intron_variant | MODIFIER | c.288+1775G>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 3/10 | chr1 | 108608027 | |||||||
| chr1:108608054 | G | C | 1 | a0001c0001t0001g0003 | 2 | NA18953.hp1 NA18956.hp2 |
intron_variant | MODIFIER | c.288+1802G>C | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 3/10 | chr1 | 108608054 | |||||||
| chr1:108608098 | C | T | 61 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(58): Show |
66 | HG00408.hp2 HG01069.hp2 HG01070.hp1 others(63): Show |
intron_variant | MODIFIER | c.288+1846C>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 3/10 | chr1 | 108608098 | |||||||
| chr1:108608358 | C | T | 2 | a0001c0001t0001g0127 a0001c0001t0001g0128 |
2 | NA18994.hp2 NA18997.hp2 |
intron_variant | MODIFIER | c.288+2106C>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 3/10 | chr1 | 108608358 | |||||||
| chr1:108609051 | G | T | 23 | a0001c0001t0003g0001 a0001c0001t0003g0237 a0001c0001t0003g0238 others(20): Show |
25 | HG00423.hp1 HG02135.hp2 HG03669.hp2 others(22): Show |
intron_variant | MODIFIER | c.288+2799G>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 3/10 | chr1 | 108609051 | |||||||
| chr1:108609149 | G | A | 1 | a0001c0001t0001g0091 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.288+2897G>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 3/10 | chr1 | 108609149 | |||||||
| chr1:108609197 | T | A | 1 | a0001c0001t0001g0072 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.288+2945T>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 3/10 | chr1 | 108609197 | |||||||
| chr1:108609339 | A | G | 230 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(227): Show |
236 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(233): Show |
intron_variant | MODIFIER | c.289-2839A>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 3/10 | chr1 | 108609339 | |||||||
| chr1:108609439 | A | G | 258 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(255): Show |
266 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(263): Show |
intron_variant | MODIFIER | c.289-2739A>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 3/10 | chr1 | 108609439 | |||||||
| chr1:108609484 | G | T | 23 | a0001c0001t0003g0001 a0001c0001t0003g0237 a0001c0001t0003g0238 others(20): Show |
25 | HG00423.hp1 HG02135.hp2 HG03669.hp2 others(22): Show |
intron_variant | MODIFIER | c.289-2694G>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 3/10 | chr1 | 108609484 | |||||||
| chr1:108609501 | A | G | 3 | a0001c0001t0002g0198 a0001c0001t0002g0199 a0001c0001t0002g0201 |
3 | HG01934.hp2 NA18971.hp1 NA18987.hp1 |
intron_variant | MODIFIER | c.289-2677A>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 3/10 | chr1 | 108609501 | |||||||
| chr1:108609660 | G | A | 1 | a0001c0001t0001g0083 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.289-2518G>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 3/10 | chr1 | 108609660 | |||||||
| chr1:108609797 | G | T | 1 | a0001c0001t0027g0183 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.289-2381G>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 3/10 | chr1 | 108609797 | |||||||
| chr1:108609965 | C | T | 5 | a0001c0001t0003g0001 a0001c0001t0003g0247 a0001c0001t0003g0254 others(2): Show |
7 | NA18956.hp1 NA18963.hp2 NA18968.hp1 others(4): Show |
intron_variant | MODIFIER | c.289-2213C>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 3/10 | chr1 | 108609965 | |||||||
| chr1:108610431 | G | A | 6 | a0001c0001t0002g0005 a0001c0001t0002g0184 a0001c0001t0002g0190 others(3): Show |
7 | HG01069.hp2 HG01071.hp2 HG02698.hp2 others(4): Show |
intron_variant | MODIFIER | c.289-1747G>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 3/10 | chr1 | 108610431 | |||||||
| chr1:108610746 | C | T | 1 | a0001c0001t0001g0092 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.289-1432C>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 3/10 | chr1 | 108610746 | |||||||
| chr1:108610807 | G | A | 7 | a0001c0001t0004g0149 a0001c0001t0004g0150 a0001c0001t0004g0151 others(4): Show |
7 | HG02572.hp1 HG02717.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.289-1371G>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 3/10 | chr1 | 108610807 | |||||||
| chr1:108610850 | C | T | 16 | a0001c0001t0004g0149 a0001c0001t0004g0150 a0001c0001t0004g0151 others(13): Show |
16 | HG01891.hp1 HG02145.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.289-1328C>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 3/10 | chr1 | 108610850 | |||||||
| chr1:108610891 | C | T | 1 | a0001c0001t0026g0246 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.289-1287C>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 3/10 | chr1 | 108610891 | |||||||
| chr1:108611095 | G | A | 1 | a0001c0001t0002g0212 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.289-1083G>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 3/10 | chr1 | 108611095 | |||||||
| chr1:108611133 | C | T | 1 | a0001c0001t0001g0068 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.289-1045C>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 3/10 | chr1 | 108611133 | |||||||
| chr1:108611149 | C | T | 77 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(74): Show |
82 | HG00408.hp2 HG01069.hp2 HG01070.hp1 others(79): Show |
intron_variant | MODIFIER | c.289-1029C>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 3/10 | chr1 | 108611149 | |||||||
| chr1:108611196 | G | T | 1 | a0001c0001t0013g0176 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.289-982G>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 3/10 | chr1 | 108611196 | |||||||
| chr1:108611278 | C | T | 1 | a0001c0001t0001g0082 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.289-900C>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 3/10 | chr1 | 108611278 | |||||||
| chr1:108611689 | A | G | 1 | a0001c0001t0005g0118 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.289-489A>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 3/10 | chr1 | 108611689 | |||||||
| chr1:108611837 | A | C | 1 | a0001c0001t0001g0111 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.289-341A>C | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 3/10 | chr1 | 108611837 | |||||||
| chr1:108611917 | G | GA | 76 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(73): Show |
81 | HG00408.hp2 HG01069.hp2 HG01070.hp1 others(78): Show |
intron_variant | MODIFIER | c.289-255dupA | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr1 | 108611917 | ||||||
| chr1:108612045 | T | C | 16 | a0001c0001t0004g0149 a0001c0001t0004g0150 a0001c0001t0004g0151 others(13): Show |
16 | HG01891.hp1 HG02145.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.289-133T>C | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 3/10 | chr1 | 108612045 | |||||||
| chr1:108612352 | G | A | 77 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(74): Show |
82 | HG00408.hp2 HG01069.hp2 HG01070.hp1 others(79): Show |
intron_variant | MODIFIER | c.405+58G>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 4/10 | chr1 | 108612352 | |||||||
| chr1:108612420 | G | A | 2 | a0001c0001t0001g0142 a0001c0001t0001g0143 |
2 | HG02165.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.405+126G>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 4/10 | chr1 | 108612420 | |||||||
| chr1:108612515 | C | T | 2 | a0001c0001t0029g0174 a0001c0001t0030g0175 |
2 | HG02630.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.405+221C>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 4/10 | chr1 | 108612515 | |||||||
| chr1:108612522 | G | A | 228 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(225): Show |
234 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(231): Show |
intron_variant | MODIFIER | c.405+228G>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 4/10 | chr1 | 108612522 | |||||||
| chr1:108612537 | A | G | 1 | a0001c0001t0024g0147 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.405+243A>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 4/10 | chr1 | 108612537 | |||||||
| chr1:108612552 | A | G | 2 | a0001c0001t0002g0008 a0001c0001t0002g0206 |
3 | HG01070.hp1 HG01074.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.405+258A>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 4/10 | chr1 | 108612552 | |||||||
| chr1:108612638 | G | A | 53 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(50): Show |
57 | HG00408.hp2 HG01070.hp1 HG01074.hp1 others(54): Show |
intron_variant | MODIFIER | c.405+344G>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 4/10 | chr1 | 108612638 | |||||||
| chr1:108612642 | C | T | 77 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(74): Show |
82 | HG00408.hp2 HG01069.hp2 HG01070.hp1 others(79): Show |
intron_variant | MODIFIER | c.405+348C>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 4/10 | chr1 | 108612642 | |||||||
| chr1:108612893 | C | A | 145 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(142): Show |
146 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(143): Show |
intron_variant | MODIFIER | c.405+599C>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 4/10 | chr1 | 108612893 | |||||||
| chr1:108612931 | T | G | 1 | a0001c0001t0007g0026 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.405+637T>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 4/10 | chr1 | 108612931 | |||||||
| chr1:108613030 | A | G | 2 | a0001c0001t0014g0234 a0001c0001t0014g0235 |
2 | HG01884.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.405+736A>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 4/10 | chr1 | 108613030 | |||||||
| chr1:108613061 | C | A | 1 | a0001c0001t0001g0074 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.405+767C>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 4/10 | chr1 | 108613061 | |||||||
| chr1:108613132 | G | A | 2 | a0001c0001t0029g0174 a0001c0001t0030g0175 |
2 | HG02630.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.405+838G>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 4/10 | chr1 | 108613132 | |||||||
| chr1:108613141 | T | G | 1 | a0001c0001t0004g0165 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.405+847T>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 4/10 | chr1 | 108613141 | |||||||
| chr1:108613308 | A | T | 5 | a0001c0001t0006g0178 a0001c0001t0006g0179 a0001c0001t0006g0180 others(2): Show |
5 | HG02559.hp1 HG02886.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.405+1014A>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 4/10 | chr1 | 108613308 | |||||||
| chr1:108613543 | T | C | 24 | a0001c0001t0003g0001 a0001c0001t0003g0237 a0001c0001t0003g0238 others(21): Show |
26 | HG00423.hp1 HG02109.hp1 HG02135.hp2 others(23): Show |
intron_variant | MODIFIER | c.405+1249T>C | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 4/10 | chr1 | 108613543 | |||||||
| chr1:108613662 | C | T | 258 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(255): Show |
266 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(263): Show |
intron_variant | MODIFIER | c.405+1368C>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 4/10 | chr1 | 108613662 | |||||||
| chr1:108613700 | G | A | 9 | a0001c0001t0001g0049 a0001c0001t0001g0063 a0001c0001t0001g0064 others(6): Show |
9 | HG00639.hp2 HG01106.hp1 HG01257.hp2 others(6): Show |
intron_variant | MODIFIER | c.405+1406G>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 4/10 | chr1 | 108613700 | |||||||
| chr1:108614132 | A | T | 2 | a0001c0001t0004g0154 a0001c0001t0004g0155 |
2 | HG02717.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.405+1838A>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 4/10 | chr1 | 108614132 | |||||||
| chr1:108614205 | T | TA | 41 | a0001c0001t0001g0035 a0001c0001t0001g0082 a0001c0001t0001g0083 others(38): Show |
43 | HG00423.hp1 HG01243.hp1 HG01243.hp2 others(40): Show |
intron_variant | MODIFIER | c.405+1934dupA | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr1 | 108614205 | ||||||
| chr1:108614205 | T | TAA | 117 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(114): Show |
118 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(115): Show |
intron_variant | MODIFIER | c.405+1933_405+1934d others(4): Show |
EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr1 | 108614205 | ||||||
| chr1:108614205 | T | TAAA | 25 | a0001c0001t0001g0041 a0001c0001t0001g0049 a0001c0001t0001g0063 others(22): Show |
25 | HG00639.hp2 HG00642.hp1 HG00642.hp2 others(22): Show |
intron_variant | MODIFIER | c.405+1932_405+1934d others(5): Show |
EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr1 | 108614205 | ||||||
| chr1:108614284 | T | A | 3 | a0001c0001t0015g0172 a0001c0001t0015g0173 a0001c0001t0032g0262 |
3 | HG02647.hp1 HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.405+1990T>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 4/10 | chr1 | 108614284 | |||||||
| chr1:108614466 | G | A | 2 | a0001c0001t0006g0181 a0001c0001t0006g0182 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.406-1916G>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 4/10 | chr1 | 108614466 | |||||||
| chr1:108614671 | C | T | 3 | a0001c0001t0001g0054 a0001c0001t0001g0056 a0001c0001t0001g0129 |
3 | NA18952.hp1 NA18963.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.406-1711C>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 4/10 | chr1 | 108614671 | |||||||
| chr1:108615014 | C | A | 1 | a0001c0001t0006g0158 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.406-1368C>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 4/10 | chr1 | 108615014 | |||||||
| chr1:108615535 | G | A | 77 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(74): Show |
82 | HG00408.hp2 HG01069.hp2 HG01070.hp1 others(79): Show |
intron_variant | MODIFIER | c.406-847G>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 4/10 | chr1 | 108615535 | |||||||
| chr1:108615544 | G | GC | 77 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(74): Show |
82 | HG00408.hp2 HG01069.hp2 HG01070.hp1 others(79): Show |
intron_variant | MODIFIER | c.406-838_406-837ins others(1): Show |
EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 4/10 | chr1 | 108615544 | |||||||
| chr1:108615611 | C | CA | 8 | a0001c0001t0001g0003 a0001c0001t0001g0039 a0001c0001t0001g0040 others(5): Show |
9 | HG00642.hp1 HG02055.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.406-761dupA | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr1 | 108615611 | ||||||
| chr1:108615629 | G | A | 258 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(255): Show |
266 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(263): Show |
intron_variant | MODIFIER | c.406-753G>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 4/10 | chr1 | 108615629 | |||||||
| chr1:108615646 | G | A | 1 | a0001c0001t0001g0080 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.406-736G>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 4/10 | chr1 | 108615646 | |||||||
| chr1:108615676 | G | T | 5 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0186 others(2): Show |
7 | HG02145.hp1 HG02622.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.406-706G>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 4/10 | chr1 | 108615676 | |||||||
| chr1:108615698 | T | A | 1 | a0001c0001t0029g0174 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.406-684T>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 4/10 | chr1 | 108615698 | |||||||
| chr1:108615786 | TA | T | 11 | a0001c0001t0001g0039 a0001c0001t0001g0053 a0001c0001t0001g0065 others(8): Show |
11 | HG01975.hp2 HG01993.hp2 HG02004.hp1 others(8): Show |
intron_variant | MODIFIER | c.406-578delA | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr1 | 108615786 | ||||||
| chr1:108615891 | C | T | 147 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(144): Show |
148 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(145): Show |
intron_variant | MODIFIER | c.406-491C>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 4/10 | chr1 | 108615891 | |||||||
| chr1:108616124 | CT | C | 210 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(207): Show |
216 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(213): Show |
intron_variant | MODIFIER | c.406-239delT | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr1 | 108616124 | ||||||
| chr1:108616124 | CTT | C | 15 | a0001c0001t0001g0033 a0001c0001t0001g0093 a0001c0001t0001g0111 others(12): Show |
15 | HG01169.hp2 HG01975.hp2 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.406-240_406-239del others(2): Show |
EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr1 | 108616124 | ||||||
| chr1:108616128 | T | C | 2 | a0001c0001t0001g0060 a0001c0001t0001g0062 |
2 | NA18968.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.406-254T>C | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 4/10 | chr1 | 108616128 | |||||||
| chr1:108616377 | T | C | 5 | a0001c0001t0006g0178 a0001c0001t0006g0179 a0001c0001t0006g0180 others(2): Show |
5 | HG02559.hp1 HG02886.hp2 HG02895.hp1 others(2): Show |
splice_region_variant&intron_variant | LOW | c.406-5T>C | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 4/10 | chr1 | 108616377 | |||||||
| chr1:108616461 | C | T | 1 | a0001c0001t0023g0132 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.452+33C>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 5/10 | chr1 | 108616461 | |||||||
| chr1:108616655 | G | A | 230 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(227): Show |
236 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(233): Show |
intron_variant | MODIFIER | c.452+227G>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 5/10 | chr1 | 108616655 | |||||||
| chr1:108616663 | C | T | 53 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(50): Show |
57 | HG00408.hp2 HG01070.hp1 HG01074.hp1 others(54): Show |
intron_variant | MODIFIER | c.452+235C>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 5/10 | chr1 | 108616663 | |||||||
| chr1:108616695 | G | A | 3 | a0001c0001t0001g0072 a0001c0001t0015g0172 a0001c0001t0015g0173 |
3 | HG01884.hp1 HG02647.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.452+267G>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 5/10 | chr1 | 108616695 | |||||||
| chr1:108617168 | T | C | 2 | a0001c0001t0009g0021 a0001c0001t0009g0023 |
2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.452+740T>C | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 5/10 | chr1 | 108617168 | |||||||
| chr1:108617223 | C | T | 1 | a0001c0001t0030g0175 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.452+795C>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 5/10 | chr1 | 108617223 | |||||||
| chr1:108617240 | A | G | 1 | a0001c0001t0001g0086 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.452+812A>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 5/10 | chr1 | 108617240 | |||||||
| chr1:108617313 | G | T | 1 | a0001c0001t0002g0229 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.452+885G>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 5/10 | chr1 | 108617313 | |||||||
| chr1:108617402 | A | T | 1 | a0001c0001t0032g0262 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.452+974A>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 5/10 | chr1 | 108617402 | |||||||
| chr1:108617508 | T | C | 1 | a0001c0001t0002g0005 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.452+1080T>C | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 5/10 | chr1 | 108617508 | |||||||
| chr1:108617575 | G | C | 1 | a0001c0001t0001g0068 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.452+1147G>C | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 5/10 | chr1 | 108617575 | |||||||
| chr1:108617658 | G | T | 3 | a0001c0001t0002g0190 a0001c0001t0002g0233 a0001c0001t0002g0236 |
3 | HG03669.hp1 HG04199.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.452+1230G>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 5/10 | chr1 | 108617658 | |||||||
| chr1:108617806 | G | A | 1 | a0001c0001t0003g0253 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.452+1378G>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 5/10 | chr1 | 108617806 | |||||||
| chr1:108617835 | T | C | 2 | a0001c0001t0024g0147 a0001c0001t0031g0148 |
2 | NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.452+1407T>C | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 5/10 | chr1 | 108617835 | |||||||
| chr1:108618117 | A | G | 16 | a0001c0001t0004g0149 a0001c0001t0004g0150 a0001c0001t0004g0151 others(13): Show |
16 | HG01891.hp1 HG02145.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.452+1689A>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 5/10 | chr1 | 108618117 | |||||||
| chr1:108618147 | A | G | 228 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(225): Show |
234 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(231): Show |
intron_variant | MODIFIER | c.452+1719A>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 5/10 | chr1 | 108618147 | |||||||
| chr1:108618300 | A | G | 1 | a0001c0001t0001g0072 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.452+1872A>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 5/10 | chr1 | 108618300 | |||||||
| chr1:108618424 | A | G | 162 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(159): Show |
163 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(160): Show |
intron_variant | MODIFIER | c.452+1996A>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 5/10 | chr1 | 108618424 | |||||||
| chr1:108618836 | C | CA | 89 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(86): Show |
91 | HG00639.hp1 HG00642.hp1 HG00642.hp2 others(88): Show |
intron_variant | MODIFIER | c.452+2423dupA | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 108618836 | ||||||
| chr1:108619012 | G | T | 1 | a0001c0001t0001g0012 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.452+2584G>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 5/10 | chr1 | 108619012 | |||||||
| chr1:108619124 | T | C | 26 | a0001c0001t0001g0010 a0001c0001t0001g0033 a0001c0001t0001g0034 others(23): Show |
26 | HG00642.hp2 HG00738.hp2 HG01106.hp2 others(23): Show |
intron_variant | MODIFIER | c.452+2696T>C | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 5/10 | chr1 | 108619124 | |||||||
| chr1:108619490 | T | C | 5 | a0001c0001t0003g0001 a0001c0001t0003g0247 a0001c0001t0003g0254 others(2): Show |
7 | NA18956.hp1 NA18963.hp2 NA18968.hp1 others(4): Show |
intron_variant | MODIFIER | c.452+3062T>C | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 5/10 | chr1 | 108619490 | |||||||
| chr1:108619523 | C | T | 223 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(220): Show |
229 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(226): Show |
intron_variant | MODIFIER | c.452+3095C>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 5/10 | chr1 | 108619523 | |||||||
| chr1:108620325 | T | C | 8 | a0001c0001t0002g0005 a0001c0001t0002g0184 a0001c0001t0002g0190 others(5): Show |
9 | HG01069.hp2 HG01071.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.452+3897T>C | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 5/10 | chr1 | 108620325 | |||||||
| chr1:108620337 | AATTATAT others(3): Show |
A | 139 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(136): Show |
140 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(137): Show |
intron_variant | MODIFIER | c.452+3912_452+3921d others(12): Show |
EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 108620337 | ||||||
| chr1:108620603 | G | A | 2 | a0001c0001t0024g0147 a0001c0001t0031g0148 |
2 | NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.453-4042G>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 5/10 | chr1 | 108620603 | |||||||
| chr1:108620622 | G | A | 2 | a0001c0001t0009g0021 a0001c0001t0009g0023 |
2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.453-4023G>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 5/10 | chr1 | 108620622 | |||||||
| chr1:108620632 | A | G | 5 | a0001c0001t0006g0178 a0001c0001t0006g0179 a0001c0001t0006g0180 others(2): Show |
5 | HG02559.hp1 HG02886.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.453-4013A>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 5/10 | chr1 | 108620632 | |||||||
| chr1:108620677 | A | T | 77 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(74): Show |
82 | HG00408.hp2 HG01069.hp2 HG01070.hp1 others(79): Show |
intron_variant | MODIFIER | c.453-3968A>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 5/10 | chr1 | 108620677 | |||||||
| chr1:108620740 | G | GAATT | 2 | a0001c0001t0001g0125 a0001c0001t0001g0126 |
2 | NA18964.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.453-3900_453-3897d others(6): Show |
EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 108620740 | ||||||
| chr1:108620831 | A | C | 1 | a0001c0001t0001g0036 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.453-3814A>C | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 5/10 | chr1 | 108620831 | |||||||
| chr1:108620948 | G | A | 23 | a0001c0001t0003g0001 a0001c0001t0003g0237 a0001c0001t0003g0238 others(20): Show |
25 | HG00423.hp1 HG02135.hp2 HG03669.hp2 others(22): Show |
intron_variant | MODIFIER | c.453-3697G>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 5/10 | chr1 | 108620948 | |||||||
| chr1:108621044 | A | G | 16 | a0001c0001t0004g0149 a0001c0001t0004g0150 a0001c0001t0004g0151 others(13): Show |
16 | HG01891.hp1 HG02145.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.453-3601A>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 5/10 | chr1 | 108621044 | |||||||
| chr1:108621047 | C | CAG | 258 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(255): Show |
266 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(263): Show |
intron_variant | MODIFIER | c.453-3598_453-3597i others(4): Show |
EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 5/10 | chr1 | 108621047 | |||||||
| chr1:108621106 | G | A | 1 | a0001c0001t0013g0171 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.453-3539G>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 5/10 | chr1 | 108621106 | |||||||
| chr1:108621189 | T | G | 1 | a0001c0001t0001g0046 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.453-3456T>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 5/10 | chr1 | 108621189 | |||||||
| chr1:108621255 | G | A | 140 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(137): Show |
141 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(138): Show |
intron_variant | MODIFIER | c.453-3390G>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 5/10 | chr1 | 108621255 | |||||||
| chr1:108621307 | A | G | 1 | a0001c0001t0002g0190 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.453-3338A>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 5/10 | chr1 | 108621307 | |||||||
| chr1:108621361 | T | C | 1 | a0001c0001t0003g0240 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.453-3284T>C | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 5/10 | chr1 | 108621361 | |||||||
| chr1:108621384 | A | G | 146 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(143): Show |
147 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(144): Show |
intron_variant | MODIFIER | c.453-3261A>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 5/10 | chr1 | 108621384 | |||||||
| chr1:108621527 | G | A | 2 | a0001c0001t0002g0194 a0001c0001t0002g0205 |
2 | HG02155.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.453-3118G>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 5/10 | chr1 | 108621527 | |||||||
| chr1:108621830 | G | GT | 80 | a0001c0001t0001g0037 a0001c0001t0001g0041 a0001c0001t0001g0042 others(77): Show |
80 | HG00408.hp1 HG00423.hp2 HG00639.hp2 others(77): Show |
intron_variant | MODIFIER | c.453-2804dupT | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 108621830 | ||||||
| chr1:108621831 | T | G | 1 | a0001c0001t0013g0171 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.453-2814T>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 5/10 | chr1 | 108621831 | |||||||
| chr1:108621947 | A | G | 3 | a0001c0001t0015g0172 a0001c0001t0015g0173 a0001c0001t0032g0262 |
3 | HG02647.hp1 HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.453-2698A>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 5/10 | chr1 | 108621947 | |||||||
| chr1:108622083 | G | A | 1 | a0001c0001t0001g0071 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.453-2562G>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 5/10 | chr1 | 108622083 | |||||||
| chr1:108622235 | G | A | 230 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(227): Show |
236 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(233): Show |
intron_variant | MODIFIER | c.453-2410G>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 5/10 | chr1 | 108622235 | |||||||
| chr1:108622300 | G | A | 2 | a0001c0001t0002g0008 a0001c0001t0002g0206 |
3 | HG01070.hp1 HG01074.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.453-2345G>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 5/10 | chr1 | 108622300 | |||||||
| chr1:108622529 | C | T | 146 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(143): Show |
147 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(144): Show |
intron_variant | MODIFIER | c.453-2116C>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 5/10 | chr1 | 108622529 | |||||||
| chr1:108622630 | T | C | 1 | a0001c0001t0013g0176 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.453-2015T>C | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 5/10 | chr1 | 108622630 | |||||||
| chr1:108622667 | C | T | 1 | a0001c0001t0004g0163 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.453-1978C>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 5/10 | chr1 | 108622667 | |||||||
| chr1:108622820 | A | G | 1 | a0001c0001t0001g0069 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.453-1825A>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 5/10 | chr1 | 108622820 | |||||||
| chr1:108622972 | T | C | 228 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(225): Show |
234 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(231): Show |
intron_variant | MODIFIER | c.453-1673T>C | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 5/10 | chr1 | 108622972 | |||||||
| chr1:108623165 | G | A | 228 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(225): Show |
234 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(231): Show |
intron_variant | MODIFIER | c.453-1480G>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 5/10 | chr1 | 108623165 | |||||||
| chr1:108623169 | C | T | 223 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(220): Show |
229 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(226): Show |
intron_variant | MODIFIER | c.453-1476C>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 5/10 | chr1 | 108623169 | |||||||
| chr1:108623235 | A | G | 1 | a0001c0001t0001g0059 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.453-1410A>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 5/10 | chr1 | 108623235 | |||||||
| chr1:108623473 | T | C | 1 | a0001c0001t0001g0125 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.453-1172T>C | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 5/10 | chr1 | 108623473 | |||||||
| chr1:108623678 | T | A | 1 | a0001c0001t0002g0177 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.453-967T>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 5/10 | chr1 | 108623678 | |||||||
| chr1:108623679 | A | T | 77 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(74): Show |
82 | HG00408.hp2 HG01069.hp2 HG01070.hp1 others(79): Show |
intron_variant | MODIFIER | c.453-966A>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 5/10 | chr1 | 108623679 | |||||||
| chr1:108623695 | G | T | 141 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(138): Show |
142 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(139): Show |
intron_variant | MODIFIER | c.453-950G>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 5/10 | chr1 | 108623695 | |||||||
| chr1:108623702 | C | T | 1 | a0001c0001t0013g0171 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.453-943C>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 5/10 | chr1 | 108623702 | |||||||
| chr1:108623711 | G | A | 7 | a0001c0001t0005g0121 a0001c0001t0005g0122 a0001c0001t0005g0123 others(4): Show |
7 | HG02647.hp1 HG02738.hp2 HG03453.hp2 others(4): Show |
intron_variant | MODIFIER | c.453-934G>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 5/10 | chr1 | 108623711 | |||||||
| chr1:108623736 | A | G | 1 | a0001c0001t0002g0198 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.453-909A>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 5/10 | chr1 | 108623736 | |||||||
| chr1:108623764 | C | T | 1 | a0001c0001t0032g0262 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.453-881C>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 5/10 | chr1 | 108623764 | |||||||
| chr1:108623765 | G | A | 146 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(143): Show |
147 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(144): Show |
intron_variant | MODIFIER | c.453-880G>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 5/10 | chr1 | 108623765 | |||||||
| chr1:108623891 | C | T | 1 | a0001c0001t0004g0153 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.453-754C>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 5/10 | chr1 | 108623891 | |||||||
| chr1:108623896 | T | A | 4 | a0001c0001t0001g0016 a0001c0001t0001g0022 a0001c0001t0001g0024 others(1): Show |
4 | HG02622.hp2 HG02965.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.453-749T>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 5/10 | chr1 | 108623896 | |||||||
| chr1:108623897 | C | T | 4 | a0001c0001t0001g0016 a0001c0001t0001g0022 a0001c0001t0001g0024 others(1): Show |
4 | HG02622.hp2 HG02965.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.453-748C>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 5/10 | chr1 | 108623897 | |||||||
| chr1:108624432 | T | TA | 26 | a0001c0001t0002g0193 a0001c0001t0003g0001 a0001c0001t0003g0237 others(23): Show |
28 | HG00423.hp1 HG02135.hp2 HG02148.hp2 others(25): Show |
intron_variant | MODIFIER | c.453-196dupA | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 108624432 | ||||||
| chr1:108624432 | T | TAA | 28 | a0001c0001t0001g0010 a0001c0001t0001g0033 a0001c0001t0001g0034 others(25): Show |
28 | HG00642.hp2 HG00738.hp2 HG01106.hp2 others(25): Show |
intron_variant | MODIFIER | c.453-197_453-196dup others(2): Show |
EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 108624432 | ||||||
| chr1:108624432 | TA | T | 13 | a0001c0001t0002g0005 a0001c0001t0002g0184 a0001c0001t0002g0190 others(10): Show |
14 | HG01069.hp2 HG01071.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.453-196delA | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 108624432 | ||||||
| chr1:108624445 | A | C | 1 | a0001c0001t0025g0161 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.453-200A>C | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 5/10 | chr1 | 108624445 | |||||||
| chr1:108624446 | A | AAC | 110 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(107): Show |
111 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(108): Show |
intron_variant | MODIFIER | c.453-198_453-197ins others(2): Show |
EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr1 | 108624446 | ||||||
| chr1:108624446 | A | AC | 9 | a0001c0001t0001g0050 a0001c0001t0001g0094 a0001c0001t0001g0145 others(6): Show |
9 | HG01169.hp1 HG01243.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.453-199_453-198ins others(1): Show |
EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 5/10 | chr1 | 108624446 | |||||||
| chr1:108624627 | G | A | 3 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 |
3 | HG03491.hp2 HG03492.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.453-18G>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 5/10 | chr1 | 108624627 | |||||||
| chr1:108625075 | G | A | 8 | a0001c0001t0002g0005 a0001c0001t0002g0184 a0001c0001t0002g0190 others(5): Show |
9 | HG01069.hp2 HG01071.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.556+327G>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 6/10 | chr1 | 108625075 | |||||||
| chr1:108625193 | G | A | 77 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(74): Show |
82 | HG00408.hp2 HG01069.hp2 HG01070.hp1 others(79): Show |
intron_variant | MODIFIER | c.556+445G>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 6/10 | chr1 | 108625193 | |||||||
| chr1:108625253 | G | A | 2 | a0001c0001t0016g0159 a0001c0001t0016g0160 |
2 | HG02258.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.556+505G>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 6/10 | chr1 | 108625253 | |||||||
| chr1:108625317 | G | A | 1 | a0001c0001t0013g0171 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.556+569G>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 6/10 | chr1 | 108625317 | |||||||
| chr1:108625528 | A | G | 5 | a0001c0001t0006g0178 a0001c0001t0006g0179 a0001c0001t0006g0180 others(2): Show |
5 | HG02559.hp1 HG02886.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.556+780A>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 6/10 | chr1 | 108625528 | |||||||
| chr1:108625649 | C | T | 1 | a0001c0001t0030g0175 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.556+901C>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 6/10 | chr1 | 108625649 | |||||||
| chr1:108625758 | A | ATC | 36 | a0001c0001t0002g0005 a0001c0001t0002g0009 a0001c0001t0002g0097 others(33): Show |
38 | HG00408.hp2 HG01069.hp2 HG01071.hp2 others(35): Show |
intron_variant | MODIFIER | c.556+1026_556+1027d others(4): Show |
EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 108625758 | ||||||
| chr1:108625770 | CTCTCTGT others(11): Show |
C | 1 | a0001c0001t0013g0176 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.556+1024_556+1041d others(20): Show |
EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 108625770 | ||||||
| chr1:108625772 | CTCTG | C | 4 | a0001c0001t0013g0171 a0001c0001t0015g0172 a0001c0001t0024g0147 others(1): Show |
4 | HG02486.hp1 HG02647.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.556+1026_556+1029d others(6): Show |
EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 108625772 | ||||||
| chr1:108625772 | CTCTGTG | C | 5 | a0001c0001t0006g0178 a0001c0001t0006g0179 a0001c0001t0006g0180 others(2): Show |
5 | HG02559.hp1 HG02886.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.556+1026_556+1031d others(8): Show |
EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 108625772 | ||||||
| chr1:108625772 | CTCTGTGT others(5): Show |
C | 2 | a0001c0001t0029g0174 a0001c0001t0032g0262 |
2 | HG02630.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.556+1026_556+1037d others(14): Show |
EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 108625772 | ||||||
| chr1:108625772 | CTCTGTGT others(7): Show |
C | 4 | a0001c0001t0005g0121 a0001c0001t0005g0122 a0001c0001t0005g0123 others(1): Show |
4 | HG02738.hp2 HG03710.hp2 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.556+1026_556+1039d others(16): Show |
EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 108625772 | ||||||
| chr1:108625774 | C | CTCTG | 10 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0195 others(7): Show |
12 | HG02145.hp1 HG02630.hp2 HG02895.hp2 others(9): Show |
intron_variant | MODIFIER | c.556+1027_556+1028i others(6): Show |
EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 108625774 | ||||||
| chr1:108625774 | C | CTCTGTGT others(1): Show |
5 | a0001c0001t0002g0189 a0001c0001t0002g0190 a0001c0001t0002g0236 others(2): Show |
5 | HG01884.hp2 HG02109.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.556+1027_556+1028i others(10): Show |
EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 108625774 | ||||||
| chr1:108625774 | CTG | C | 5 | a0001c0001t0002g0201 a0001c0001t0002g0210 a0001c0001t0002g0225 others(2): Show |
5 | HG01891.hp2 HG01934.hp2 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.556+1079_556+1080d others(4): Show |
EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 108625774 | ||||||
| chr1:108625774 | CTGTGTGT others(3): Show |
C | 26 | a0001c0001t0001g0012 a0001c0001t0001g0016 a0001c0001t0001g0022 others(23): Show |
26 | HG00639.hp1 HG00735.hp1 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.556+1071_556+1080d others(12): Show |
EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 108625774 | ||||||
| chr1:108625774 | CTGTGTGT others(5): Show |
C | 14 | a0001c0001t0001g0015 a0001c0001t0001g0052 a0001c0001t0001g0056 others(11): Show |
14 | HG00642.hp1 HG00735.hp2 HG01361.hp1 others(11): Show |
intron_variant | MODIFIER | c.556+1069_556+1080d others(14): Show |
EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 108625774 | ||||||
| chr1:108625774 | CTGTGTGT others(7): Show |
C | 106 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(103): Show |
108 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.556+1067_556+1080d others(16): Show |
EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 108625774 | ||||||
| chr1:108625774 | CTGTGTGT others(9): Show |
C | 4 | a0001c0001t0001g0077 a0001c0001t0001g0103 a0001c0001t0001g0104 others(1): Show |
4 | HG01975.hp1 HG02055.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.556+1065_556+1080d others(18): Show |
EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 108625774 | ||||||
| chr1:108625774 | CTGTGTGT others(11): Show |
C | 6 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(3): Show |
6 | HG00738.hp2 HG01169.hp2 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.556+1063_556+1080d others(20): Show |
EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 108625774 | ||||||
| chr1:108625776 | G | C | 20 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0002g0177 others(17): Show |
21 | HG01070.hp1 HG01074.hp1 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.556+1028G>C | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 6/10 | chr1 | 108625776 | |||||||
| chr1:108625778 | G | C | 4 | a0001c0001t0002g0201 a0001c0001t0002g0210 a0001c0001t0002g0225 others(1): Show |
4 | HG01934.hp2 HG01975.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.556+1030G>C | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 6/10 | chr1 | 108625778 | |||||||
| chr1:108625780 | G | C | 2 | a0001c0001t0002g0201 a0001c0001t0004g0150 |
2 | HG01934.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.556+1032G>C | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 6/10 | chr1 | 108625780 | |||||||
| chr1:108625782 | G | C | 1 | a0001c0001t0002g0222 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.556+1034G>C | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 6/10 | chr1 | 108625782 | |||||||
| chr1:108625788 | G | C | 1 | a0001c0001t0026g0246 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.556+1040G>C | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 6/10 | chr1 | 108625788 | |||||||
| chr1:108625790 | G | C | 3 | a0001c0001t0001g0107 a0001c0001t0001g0109 a0001c0001t0001g0110 |
3 | NA18947.hp2 NA19068.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.556+1042G>C | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 6/10 | chr1 | 108625790 | |||||||
| chr1:108625792 | GTGTGTGT others(6): Show |
G | 1 | a0001c0001t0001g0042 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.556+1045_556+1057d others(15): Show |
EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 6/10 | chr1 | 108625792 | |||||||
| chr1:108625796 | GTGTGTGT others(6): Show |
G | 1 | a0001c0001t0001g0261 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.556+1049_556+1061d others(15): Show |
EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 6/10 | chr1 | 108625796 | |||||||
| chr1:108625802 | GTGTGTGT others(6): Show |
G | 1 | a0001c0001t0001g0093 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.556+1055_556+1067d others(15): Show |
EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 6/10 | chr1 | 108625802 | |||||||
| chr1:108625810 | G | C | 1 | a0001c0001t0001g0261 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.556+1062G>C | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 6/10 | chr1 | 108625810 | |||||||
| chr1:108625820 | G | T | 1 | a0001c0001t0013g0176 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.556+1072G>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 6/10 | chr1 | 108625820 | |||||||
| chr1:108625822 | G | T | 205 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(202): Show |
211 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(208): Show |
intron_variant | MODIFIER | c.556+1074G>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 6/10 | chr1 | 108625822 | |||||||
| chr1:108625827 | T | G | 1 | a0001c0001t0013g0176 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.556+1079T>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 6/10 | chr1 | 108625827 | |||||||
| chr1:108625828 | G | A | 1 | a0001c0001t0013g0176 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.556+1080G>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 6/10 | chr1 | 108625828 | |||||||
| chr1:108625829 | G | T | 3 | a0001c0001t0015g0172 a0001c0001t0015g0173 a0001c0001t0032g0262 |
3 | HG02647.hp1 HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.556+1081G>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 6/10 | chr1 | 108625829 | |||||||
| chr1:108625883 | T | G | 5 | a0001c0001t0006g0178 a0001c0001t0006g0179 a0001c0001t0006g0180 others(2): Show |
5 | HG02559.hp1 HG02886.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.556+1135T>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 6/10 | chr1 | 108625883 | |||||||
| chr1:108625978 | G | C | 1 | a0001c0001t0001g0145 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.556+1230G>C | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 6/10 | chr1 | 108625978 | |||||||
| chr1:108626064 | G | A | 23 | a0001c0001t0003g0001 a0001c0001t0003g0237 a0001c0001t0003g0238 others(20): Show |
25 | HG00423.hp1 HG02135.hp2 HG03669.hp2 others(22): Show |
intron_variant | MODIFIER | c.556+1316G>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 6/10 | chr1 | 108626064 | |||||||
| chr1:108626195 | T | C | 3 | a0001c0001t0001g0046 a0001c0001t0001g0084 a0001c0001t0001g0085 |
3 | HG01074.hp2 HG01981.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.556+1447T>C | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 6/10 | chr1 | 108626195 | |||||||
| chr1:108626440 | C | T | 1 | a0001c0001t0001g0046 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.556+1692C>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 6/10 | chr1 | 108626440 | |||||||
| chr1:108626643 | T | C | 2 | a0001c0001t0015g0172 a0001c0001t0015g0173 |
2 | HG02647.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.557-1524T>C | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 6/10 | chr1 | 108626643 | |||||||
| chr1:108626976 | A | G | 1 | a0001c0001t0006g0158 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.557-1191A>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 6/10 | chr1 | 108626976 | |||||||
| chr1:108627174 | G | A | 2 | a0001c0001t0029g0174 a0001c0001t0030g0175 |
2 | HG02630.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.557-993G>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 6/10 | chr1 | 108627174 | |||||||
| chr1:108627179 | A | G | 8 | a0001c0001t0002g0005 a0001c0001t0002g0184 a0001c0001t0002g0190 others(5): Show |
9 | HG01069.hp2 HG01071.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.557-988A>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 6/10 | chr1 | 108627179 | |||||||
| chr1:108627577 | A | C | 169 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(166): Show |
172 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(169): Show |
intron_variant | MODIFIER | c.557-590A>C | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 6/10 | chr1 | 108627577 | |||||||
| chr1:108627627 | C | G | 2 | a0001c0001t0013g0171 a0001c0001t0013g0176 |
2 | HG02486.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.557-540C>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 6/10 | chr1 | 108627627 | |||||||
| chr1:108627726 | G | T | 1 | a0001c0001t0001g0037 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.557-441G>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 6/10 | chr1 | 108627726 | |||||||
| chr1:108627740 | A | G | 2 | a0001c0001t0001g0003 a0001c0001t0001g0093 |
3 | NA18953.hp1 NA18956.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.557-427A>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 6/10 | chr1 | 108627740 | |||||||
| chr1:108627766 | C | T | 9 | a0001c0001t0003g0237 a0001c0001t0003g0238 a0001c0001t0003g0239 others(6): Show |
9 | HG00423.hp1 NA18944.hp1 NA18947.hp1 others(6): Show |
intron_variant | MODIFIER | c.557-401C>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 6/10 | chr1 | 108627766 | |||||||
| chr1:108627786 | G | A | 1 | a0001c0001t0001g0094 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.557-381G>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 6/10 | chr1 | 108627786 | |||||||
| chr1:108627857 | T | C | 169 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(166): Show |
172 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(169): Show |
intron_variant | MODIFIER | c.557-310T>C | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 6/10 | chr1 | 108627857 | |||||||
| chr1:108628119 | A | G | 1 | a0001c0001t0003g0256 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.557-48A>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 6/10 | chr1 | 108628119 | |||||||
| chr1:108628120 | T | C | 5 | a0001c0001t0006g0178 a0001c0001t0006g0179 a0001c0001t0006g0180 others(2): Show |
5 | HG02559.hp1 HG02886.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.557-47T>C | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 6/10 | chr1 | 108628120 | |||||||
| chr1:108628124 | C | T | 141 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(138): Show |
142 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(139): Show |
intron_variant | MODIFIER | c.557-43C>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 6/10 | chr1 | 108628124 | |||||||
| chr1:108628598 | T | G | 3 | a0001c0001t0001g0032 a0001c0001t0011g0027 a0001c0001t0011g0028 |
3 | HG00639.hp1 HG00738.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.842+14T>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 8/10 | chr1 | 108628598 | |||||||
| chr1:108629001 | C | T | 61 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(58): Show |
66 | HG00408.hp2 HG01069.hp2 HG01070.hp1 others(63): Show |
intron_variant | MODIFIER | c.970+197C>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 9/10 | chr1 | 108629001 | |||||||
| chr1:108629079 | C | T | 1 | a0001c0001t0001g0025 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.970+275C>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 9/10 | chr1 | 108629079 | |||||||
| chr1:108629221 | T | G | 4 | a0001c0001t0001g0016 a0001c0001t0001g0022 a0001c0001t0001g0024 others(1): Show |
4 | HG02622.hp2 HG02965.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.971-367T>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 9/10 | chr1 | 108629221 | |||||||
| chr1:108629349 | C | G | 85 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(82): Show |
90 | HG00408.hp2 HG01069.hp2 HG01070.hp1 others(87): Show |
intron_variant | MODIFIER | c.971-239C>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 9/10 | chr1 | 108629349 | |||||||
| chr1:108629402 | T | G | 1 | a0001c0001t0001g0104 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.971-186T>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 9/10 | chr1 | 108629402 | |||||||
| chr1:108629442 | A | G | 2 | a0001c0001t0024g0147 a0001c0001t0031g0148 |
2 | NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.971-146A>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 9/10 | chr1 | 108629442 | |||||||
| chr1:108629508 | A | G | 1 | a0001c0001t0002g0221 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.971-80A>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 9/10 | chr1 | 108629508 | |||||||
| chr1:108629578 | T | C | 3 | a0001c0001t0002g0191 a0001c0001t0002g0196 a0001c0001t0002g0197 |
3 | HG00408.hp2 HG02027.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.971-10T>C | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 9/10 | chr1 | 108629578 | |||||||
| chr1:108629704 | T | A | 1 | a0001c0001t0001g0091 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1040+47T>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 10/10 | chr1 | 108629704 | |||||||
| chr1:108629747 | T | C | 1 | a0001c0001t0004g0166 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1040+90T>C | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 10/10 | chr1 | 108629747 | |||||||
| chr1:108629971 | C | T | 258 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(255): Show |
266 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(263): Show |
intron_variant | MODIFIER | c.1040+314C>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 10/10 | chr1 | 108629971 | |||||||
| chr1:108630067 | C | T | 1 | a0001c0001t0001g0092 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1040+410C>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 10/10 | chr1 | 108630067 | |||||||
| chr1:108630131 | A | G | 6 | a0001c0001t0003g0239 a0001c0001t0003g0240 a0001c0001t0003g0241 others(3): Show |
6 | HG00423.hp1 NA18944.hp1 NA18947.hp1 others(3): Show |
intron_variant | MODIFIER | c.1040+474A>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 10/10 | chr1 | 108630131 | |||||||
| chr1:108630140 | C | T | 1 | a0001c0001t0032g0262 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1040+483C>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 10/10 | chr1 | 108630140 | |||||||
| chr1:108630141 | G | A | 1 | a0001c0001t0001g0015 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1040+484G>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 10/10 | chr1 | 108630141 | |||||||
| chr1:108630156 | T | C | 1 | a0001c0001t0005g0114 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1040+499T>C | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 10/10 | chr1 | 108630156 | |||||||
| chr1:108630207 | G | A | 25 | a0001c0001t0003g0001 a0001c0001t0003g0237 a0001c0001t0003g0238 others(22): Show |
27 | HG00423.hp1 HG02135.hp2 HG02258.hp2 others(24): Show |
intron_variant | MODIFIER | c.1040+550G>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 10/10 | chr1 | 108630207 | |||||||
| chr1:108630287 | C | G | 1 | a0001c0001t0025g0161 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1040+630C>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 10/10 | chr1 | 108630287 | |||||||
| chr1:108630446 | GA | G | 119 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(116): Show |
126 | HG00408.hp2 HG00423.hp1 HG01069.hp2 others(123): Show |
intron_variant | MODIFIER | c.1040+791delA | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr1 | 108630446 | ||||||
| chr1:108630465 | AC | A | 61 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(58): Show |
66 | HG00408.hp2 HG01069.hp2 HG01070.hp1 others(63): Show |
intron_variant | MODIFIER | c.1040+810delC | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr1 | 108630465 | ||||||
| chr1:108630541 | G | A | 105 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(102): Show |
112 | HG00408.hp2 HG00423.hp1 HG01069.hp2 others(109): Show |
intron_variant | MODIFIER | c.1040+884G>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 10/10 | chr1 | 108630541 | |||||||
| chr1:108630750 | A | G | 23 | a0001c0001t0003g0001 a0001c0001t0003g0237 a0001c0001t0003g0238 others(20): Show |
25 | HG00423.hp1 HG02135.hp2 HG03669.hp2 others(22): Show |
intron_variant | MODIFIER | c.1040+1093A>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 10/10 | chr1 | 108630750 | |||||||
| chr1:108631040 | G | A | 16 | a0001c0001t0004g0149 a0001c0001t0004g0150 a0001c0001t0004g0151 others(13): Show |
16 | HG01891.hp1 HG02145.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.1040+1383G>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 10/10 | chr1 | 108631040 | |||||||
| chr1:108631088 | G | A | 61 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(58): Show |
66 | HG00408.hp2 HG01069.hp2 HG01070.hp1 others(63): Show |
intron_variant | MODIFIER | c.1040+1431G>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 10/10 | chr1 | 108631088 | |||||||
| chr1:108631527 | G | T | 4 | a0001c0001t0006g0178 a0001c0001t0006g0180 a0001c0001t0006g0181 others(1): Show |
4 | HG02886.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1040+1870G>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 10/10 | chr1 | 108631527 | |||||||
| chr1:108631548 | A | G | 1 | a0001c0001t0001g0092 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1040+1891A>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 10/10 | chr1 | 108631548 | |||||||
| chr1:108631640 | T | C | 9 | a0001c0001t0004g0162 a0001c0001t0004g0163 a0001c0001t0004g0164 others(6): Show |
9 | HG01891.hp1 HG02145.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1040+1983T>C | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 10/10 | chr1 | 108631640 | |||||||
| chr1:108631962 | AAATTAG | A | 3 | a0001c0001t0001g0054 a0001c0001t0001g0056 a0001c0001t0001g0129 |
3 | NA18952.hp1 NA18963.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.1040+2306_1040+231 others(10): Show |
EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 10/10 | chr1 | 108631962 | |||||||
| chr1:108631972 | G | A | 61 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(58): Show |
66 | HG00408.hp2 HG01069.hp2 HG01070.hp1 others(63): Show |
intron_variant | MODIFIER | c.1040+2315G>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 10/10 | chr1 | 108631972 | |||||||
| chr1:108632055 | G | A | 79 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(76): Show |
84 | HG00408.hp2 HG01069.hp2 HG01070.hp1 others(81): Show |
intron_variant | MODIFIER | c.1040+2398G>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 10/10 | chr1 | 108632055 | |||||||
| chr1:108632092 | C | T | 1 | a0001c0001t0032g0262 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1040+2435C>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 10/10 | chr1 | 108632092 | |||||||
| chr1:108632134 | A | AG | 98 | a0001c0001t0001g0039 a0001c0001t0001g0059 a0001c0001t0001g0093 others(95): Show |
105 | HG00408.hp2 HG00423.hp1 HG01069.hp2 others(102): Show |
intron_variant | MODIFIER | c.1040+2477_1040+247 others(5): Show |
EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 10/10 | chr1 | 108632134 | |||||||
| chr1:108632134 | A | G | 7 | a0001c0001t0001g0129 a0001c0001t0002g0194 a0001c0001t0002g0218 others(4): Show |
7 | HG02155.hp1 HG02895.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.1040+2477A>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 10/10 | chr1 | 108632134 | |||||||
| chr1:108632135 | A | AAGG | 15 | a0001c0001t0001g0046 a0001c0001t0001g0083 a0001c0001t0001g0096 others(12): Show |
15 | HG01981.hp1 HG02027.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.1040+2480_1040+248 others(7): Show |
EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr1 | 108632135 | ||||||
| chr1:108632135 | A | AGG | 130 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(127): Show |
131 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(128): Show |
intron_variant | MODIFIER | c.1040+2478_1040+247 others(6): Show |
EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 10/10 | chr1 | 108632135 | |||||||
| chr1:108632135 | A | G | 105 | a0001c0001t0001g0039 a0001c0001t0001g0059 a0001c0001t0001g0093 others(102): Show |
112 | HG00408.hp2 HG00423.hp1 HG01069.hp2 others(109): Show |
intron_variant | MODIFIER | c.1040+2478A>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 10/10 | chr1 | 108632135 | |||||||
| chr1:108632138 | A | G | 6 | a0001c0001t0001g0073 a0001c0001t0001g0094 a0001c0001t0001g0113 others(3): Show |
6 | HG01069.hp1 HG01169.hp1 HG01243.hp1 others(3): Show |
intron_variant | MODIFIER | c.1040+2481A>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 10/10 | chr1 | 108632138 | |||||||
| chr1:108632245 | A | G | 1 | a0001c0001t0001g0067 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1040+2588A>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 10/10 | chr1 | 108632245 | |||||||
| chr1:108632337 | A | G | 2 | a0001c0001t0024g0147 a0001c0001t0031g0148 |
2 | NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1040+2680A>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 10/10 | chr1 | 108632337 | |||||||
| chr1:108632471 | G | A | 6 | a0001c0001t0024g0147 a0001c0001t0025g0161 a0001c0001t0029g0174 others(3): Show |
6 | HG02055.hp1 HG02630.hp1 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.1041-2637G>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 10/10 | chr1 | 108632471 | |||||||
| chr1:108632774 | A | AG | 85 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(82): Show |
90 | HG00408.hp2 HG01069.hp2 HG01070.hp1 others(87): Show |
intron_variant | MODIFIER | c.1041-2333dupG | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr1 | 108632774 | ||||||
| chr1:108632946 | A | AT | 34 | a0001c0001t0002g0215 a0001c0001t0003g0001 a0001c0001t0003g0237 others(31): Show |
36 | HG00423.hp1 HG02109.hp1 HG02258.hp2 others(33): Show |
intron_variant | MODIFIER | c.1041-2143dupT | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr1 | 108632946 | ||||||
| chr1:108632946 | A | ATT | 201 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(198): Show |
207 | HG00408.hp1 HG00408.hp2 HG00639.hp1 others(204): Show |
intron_variant | MODIFIER | c.1041-2144_1041-214 others(6): Show |
EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr1 | 108632946 | ||||||
| chr1:108632946 | A | ATTT | 20 | a0001c0001t0001g0045 a0001c0001t0001g0060 a0001c0001t0001g0061 others(17): Show |
20 | HG00423.hp2 HG01243.hp1 HG01978.hp1 others(17): Show |
intron_variant | MODIFIER | c.1041-2145_1041-214 others(7): Show |
EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr1 | 108632946 | ||||||
| chr1:108633215 | A | G | 1 | a0001c0001t0001g0092 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1041-1893A>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 10/10 | chr1 | 108633215 | |||||||
| chr1:108633419 | C | T | 1 | a0001c0001t0013g0171 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1041-1689C>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 10/10 | chr1 | 108633419 | |||||||
| chr1:108633552 | C | G | 1 | a0001c0001t0032g0262 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1041-1556C>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 10/10 | chr1 | 108633552 | |||||||
| chr1:108633614 | T | G | 1 | a0001c0001t0013g0171 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1041-1494T>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 10/10 | chr1 | 108633614 | |||||||
| chr1:108633631 | T | C | 1 | a0001c0001t0002g0177 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1041-1477T>C | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 10/10 | chr1 | 108633631 | |||||||
| chr1:108633815 | A | G | 1 | a0001c0001t0005g0117 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1041-1293A>G | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 10/10 | chr1 | 108633815 | |||||||
| chr1:108634113 | G | GA | 2 | a0001c0001t0001g0003 a0001c0001t0001g0093 |
3 | NA18953.hp1 NA18956.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.1041-991dupA | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr1 | 108634113 | ||||||
| chr1:108634222 | T | A | 1 | a0001c0001t0025g0161 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1041-886T>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 10/10 | chr1 | 108634222 | |||||||
| chr1:108634754 | T | C | 85 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(82): Show |
90 | HG00408.hp2 HG01069.hp2 HG01070.hp1 others(87): Show |
intron_variant | MODIFIER | c.1041-354T>C | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 10/10 | chr1 | 108634754 | |||||||
| chr1:108634800 | A | C | 56 | a0001c0001t0001g0037 a0001c0001t0001g0041 a0001c0001t0001g0042 others(53): Show |
56 | HG00408.hp1 HG00423.hp2 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.1041-308A>C | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 10/10 | chr1 | 108634800 | |||||||
| chr1:108634848 | G | A | 5 | a0001c0001t0006g0178 a0001c0001t0006g0179 a0001c0001t0006g0180 others(2): Show |
5 | HG02559.hp1 HG02886.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1041-260G>A | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 10/10 | chr1 | 108634848 | |||||||
| chr1:108634940 | A | T | 2 | a0001c0001t0016g0159 a0001c0001t0016g0160 |
2 | HG02258.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1041-168A>T | EEIG2 | ENSG00000162636.16 | transcript | ENST00000370035.8 | protein_coding | 10/10 | chr1 | 108634940 |