Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 1969 |
| ensemblid | ENSG00000142627.13 |
| hgncid | 3386 |
| symbol | EPHA2 |
| name | EPH receptor A2 |
| refseq_nuc | NM_004431.5 |
| refseq_prot | NP_004422.2 |
| ensembl_nuc | ENST00000358432.8 |
| ensembl_prot | ENSP00000351209.5 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 16124337 |
| end | 16156069 |
| strand | - |
| ver | v1.2 |
| region | chr1:16124337-16156069 |
| region5000 | chr1:16119337-16161069 |
| regionname0 | EPHA2_chr1_16124337_16156069 |
| regionname5000 | EPHA2_chr1_16119337_16161069 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 976 | 283 | 77 | 60 | 88 | 16 | 40 | 58 | EPHA2_chr1_16119337_16161069 | EPHA2 | MELQA others(971): Show |
chr1 | 16119337 | 16161069 |
| a0002 | 0/0 | 976 | 8 | 8 | 0 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | MELQA others(971): Show |
chr1 | 16119337 | 16161069 |
| a0003 | 0/0 | 976 | 7 | 0 | 7 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | MELQA others(971): Show |
chr1 | 16119337 | 16161069 |
| a0004 | 0/0 | 976 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | MELQA others(971): Show |
chr1 | 16119337 | 16161069 |
| a0005 | 0/0 | 976 | 2 | 0 | 1 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | MELQA others(971): Show |
chr1 | 16119337 | 16161069 |
| a0006 | 0/0 | 976 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | MELQA others(971): Show |
chr1 | 16119337 | 16161069 |
| a0007 | 0/0 | 976 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | MELQA others(971): Show |
chr1 | 16119337 | 16161069 |
| a0008 | 0/0 | 976 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | MELQA others(971): Show |
chr1 | 16119337 | 16161069 |
| a0009 | 0/0 | 976 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | MELQA others(971): Show |
chr1 | 16119337 | 16161069 |
| a0010 | 0/0 | 976 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | MELQA others(971): Show |
chr1 | 16119337 | 16161069 |
| a0011 | 0/0 | 976 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | MELQA others(971): Show |
chr1 | 16119337 | 16161069 |
| a0012 | 0/0 | 976 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | MELQA others(971): Show |
chr1 | 16119337 | 16161069 |
| a0013 | 0/0 | 976 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | MELQA others(971): Show |
chr1 | 16119337 | 16161069 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 2928 | 116 | 7 | 28 | 58 | 4 | 18 | EPHA2_chr1_16119337_16161069 | EPHA2 | ATGGA others(2923): Show |
chr1 | 16119337 | 16161069 | ||
| a0001c0002 | 0/0 | 2928 | 33 | 12 | 8 | 11 | 1 | 1 | EPHA2_chr1_16119337_16161069 | EPHA2 | ATGGA others(2923): Show |
chr1 | 16119337 | 16161069 | ||
| a0001c0003 | 0/1 | 2928 | 30 | 6 | 4 | 11 | 2 | 6 | EPHA2_chr1_16119337_16161069 | EPHA2 | ATGGA others(2923): Show |
chr1 | 16119337 | 16161069 | ||
| a0001c0004 | 0/0 | 2928 | 29 | 26 | 1 | 0 | 0 | 2 | EPHA2_chr1_16119337_16161069 | EPHA2 | ATGGA others(2923): Show |
chr1 | 16119337 | 16161069 | ||
| a0001c0005 | 0/0 | 2928 | 24 | 13 | 4 | 0 | 3 | 4 | EPHA2_chr1_16119337_16161069 | EPHA2 | ATGGA others(2923): Show |
chr1 | 16119337 | 16161069 | ||
| a0001c0006 | 0/0 | 2928 | 20 | 0 | 5 | 5 | 3 | 7 | EPHA2_chr1_16119337_16161069 | EPHA2 | ATGGA others(2923): Show |
chr1 | 16119337 | 16161069 | ||
| a0001c0009 | 0/0 | 2928 | 6 | 2 | 4 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | ATGGA others(2923): Show |
chr1 | 16119337 | 16161069 | ||
| a0001c0010 | 0/0 | 2928 | 4 | 1 | 1 | 1 | 0 | 1 | EPHA2_chr1_16119337_16161069 | EPHA2 | ATGGA others(2923): Show |
chr1 | 16119337 | 16161069 | ||
| a0001c0012 | 0/0 | 2928 | 3 | 2 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | ATGGA others(2923): Show |
chr1 | 16119337 | 16161069 | ||
| a0001c0014 | 0/0 | 2928 | 2 | 0 | 1 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | ATGGA others(2923): Show |
chr1 | 16119337 | 16161069 | ||
| a0001c0015 | 0/0 | 2928 | 2 | 1 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | ATGGA others(2923): Show |
chr1 | 16119337 | 16161069 | ||
| a0001c0016 | 0/0 | 2928 | 2 | 0 | 0 | 0 | 2 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | ATGGA others(2923): Show |
chr1 | 16119337 | 16161069 | ||
| a0001c0018 | 0/0 | 2928 | 2 | 2 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | ATGGA others(2923): Show |
chr1 | 16119337 | 16161069 | ||
| a0001c0023 | 0/0 | 2928 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | ATGGA others(2923): Show |
chr1 | 16119337 | 16161069 | ||
| a0001c0024 | 0/0 | 2928 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | ATGGA others(2923): Show |
chr1 | 16119337 | 16161069 | ||
| a0001c0026 | 0/0 | 2928 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | ATGGA others(2923): Show |
chr1 | 16119337 | 16161069 | ||
| a0001c0027 | 0/0 | 2928 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | ATGGA others(2923): Show |
chr1 | 16119337 | 16161069 | ||
| a0001c0030 | 0/0 | 2928 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | ATGGA others(2923): Show |
chr1 | 16119337 | 16161069 | ||
| a0001c0031 | 0/0 | 2928 | 1 | 0 | 0 | 0 | 1 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | ATGGA others(2923): Show |
chr1 | 16119337 | 16161069 | ||
| a0001c0032 | 0/0 | 2928 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | ATGGA others(2923): Show |
chr1 | 16119337 | 16161069 | ||
| a0001c0033 | 0/0 | 2928 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA2_chr1_16119337_16161069 | EPHA2 | ATGGA others(2923): Show |
chr1 | 16119337 | 16161069 | ||
| a0001c0034 | 0/0 | 2928 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | ATGGA others(2923): Show |
chr1 | 16119337 | 16161069 | ||
| a0001c0036 | 0/0 | 2928 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | ATGGA others(2923): Show |
chr1 | 16119337 | 16161069 | ||
| a0002c0008 | 0/0 | 2928 | 7 | 7 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | ATGGA others(2923): Show |
chr1 | 16119337 | 16161069 | ||
| a0002c0035 | 0/0 | 2928 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | ATGGA others(2923): Show |
chr1 | 16119337 | 16161069 | ||
| a0003c0007 | 0/0 | 2928 | 7 | 0 | 7 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | ATGGA others(2923): Show |
chr1 | 16119337 | 16161069 | ||
| a0004c0011 | 0/0 | 2928 | 3 | 3 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | ATGGA others(2923): Show |
chr1 | 16119337 | 16161069 | ||
| a0005c0017 | 0/0 | 2928 | 2 | 0 | 1 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | ATGGA others(2923): Show |
chr1 | 16119337 | 16161069 | ||
| a0006c0013 | 0/0 | 2928 | 2 | 2 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | ATGGA others(2923): Show |
chr1 | 16119337 | 16161069 | ||
| a0007c0022 | 0/0 | 2928 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | ATGGA others(2923): Show |
chr1 | 16119337 | 16161069 | ||
| a0008c0020 | 0/0 | 2928 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | ATGGA others(2923): Show |
chr1 | 16119337 | 16161069 | ||
| a0009c0029 | 0/0 | 2928 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | ATGGA others(2923): Show |
chr1 | 16119337 | 16161069 | ||
| a0010c0021 | 0/0 | 2928 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | ATGGA others(2923): Show |
chr1 | 16119337 | 16161069 | ||
| a0011c0028 | 0/0 | 2928 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA2_chr1_16119337_16161069 | EPHA2 | ATGGA others(2923): Show |
chr1 | 16119337 | 16161069 | ||
| a0012c0019 | 0/0 | 2928 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | ATGGA others(2923): Show |
chr1 | 16119337 | 16161069 | ||
| a0013c0025 | 0/0 | 2928 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA2_chr1_16119337_16161069 | EPHA2 | ATGGA others(2923): Show |
chr1 | 16119337 | 16161069 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3946 | 104 | 7 | 27 | 50 | 4 | 16 | EPHA2_chr1_16119337_16161069 | EPHA2 | ATTAA others(3941): Show |
chr1 | 16119337 | 16161069 |
| a0001c0001t0002 | 1/0 | 3946 | 11 | 0 | 1 | 7 | 0 | 2 | EPHA2_chr1_16119337_16161069 | EPHA2 | ATTAA others(3941): Show |
chr1 | 16119337 | 16161069 |
| a0001c0001t0006 | 0/0 | 3946 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | ATTAA others(3941): Show |
chr1 | 16119337 | 16161069 |
| a0001c0002t0001 | 0/0 | 3946 | 20 | 10 | 5 | 3 | 1 | 1 | EPHA2_chr1_16119337_16161069 | EPHA2 | ATTAA others(3941): Show |
chr1 | 16119337 | 16161069 |
| a0001c0002t0002 | 0/0 | 3946 | 10 | 2 | 3 | 5 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | ATTAA others(3941): Show |
chr1 | 16119337 | 16161069 |
| a0001c0002t0004 | 0/0 | 3946 | 3 | 0 | 0 | 3 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | ATTAA others(3941): Show |
chr1 | 16119337 | 16161069 |
| a0001c0003t0001 | 0/1 | 3946 | 30 | 6 | 4 | 11 | 2 | 6 | EPHA2_chr1_16119337_16161069 | EPHA2 | ATTAA others(3941): Show |
chr1 | 16119337 | 16161069 |
| a0001c0004t0001 | 0/0 | 3946 | 24 | 21 | 1 | 0 | 0 | 2 | EPHA2_chr1_16119337_16161069 | EPHA2 | ATTAA others(3941): Show |
chr1 | 16119337 | 16161069 |
| a0001c0004t0002 | 0/0 | 3946 | 5 | 5 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | ATTAA others(3941): Show |
chr1 | 16119337 | 16161069 |
| a0001c0005t0001 | 0/0 | 3946 | 23 | 12 | 4 | 0 | 3 | 4 | EPHA2_chr1_16119337_16161069 | EPHA2 | ATTAA others(3941): Show |
chr1 | 16119337 | 16161069 |
| a0001c0005t0007 | 0/0 | 3946 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | ATTAA others(3941): Show |
chr1 | 16119337 | 16161069 |
| a0001c0006t0001 | 0/0 | 3946 | 20 | 0 | 5 | 5 | 3 | 7 | EPHA2_chr1_16119337_16161069 | EPHA2 | ATTAA others(3941): Show |
chr1 | 16119337 | 16161069 |
| a0001c0009t0001 | 0/0 | 3946 | 6 | 2 | 4 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | ATTAA others(3941): Show |
chr1 | 16119337 | 16161069 |
| a0001c0010t0001 | 0/0 | 3946 | 4 | 1 | 1 | 1 | 0 | 1 | EPHA2_chr1_16119337_16161069 | EPHA2 | ATTAA others(3941): Show |
chr1 | 16119337 | 16161069 |
| a0001c0012t0001 | 0/0 | 3946 | 3 | 2 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | ATTAA others(3941): Show |
chr1 | 16119337 | 16161069 |
| a0001c0014t0001 | 0/0 | 3946 | 2 | 0 | 1 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | ATTAA others(3941): Show |
chr1 | 16119337 | 16161069 |
| a0001c0015t0001 | 0/0 | 3946 | 2 | 1 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | ATTAA others(3941): Show |
chr1 | 16119337 | 16161069 |
| a0001c0016t0001 | 0/0 | 3946 | 2 | 0 | 0 | 0 | 2 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | ATTAA others(3941): Show |
chr1 | 16119337 | 16161069 |
| a0001c0018t0002 | 0/0 | 3946 | 2 | 2 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | ATTAA others(3941): Show |
chr1 | 16119337 | 16161069 |
| a0001c0023t0002 | 0/0 | 3946 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | ATTAA others(3941): Show |
chr1 | 16119337 | 16161069 |
| a0001c0024t0003 | 0/0 | 3946 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | ATTAA others(3941): Show |
chr1 | 16119337 | 16161069 |
| a0001c0026t0001 | 0/0 | 3946 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | ATTAA others(3941): Show |
chr1 | 16119337 | 16161069 |
| a0001c0027t0001 | 0/0 | 3946 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | ATTAA others(3941): Show |
chr1 | 16119337 | 16161069 |
| a0001c0030t0001 | 0/0 | 3946 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | ATTAA others(3941): Show |
chr1 | 16119337 | 16161069 |
| a0001c0031t0001 | 0/0 | 3946 | 1 | 0 | 0 | 0 | 1 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | ATTAA others(3941): Show |
chr1 | 16119337 | 16161069 |
| a0001c0032t0001 | 0/0 | 3946 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | ATTAA others(3941): Show |
chr1 | 16119337 | 16161069 |
| a0001c0033t0001 | 0/0 | 3946 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA2_chr1_16119337_16161069 | EPHA2 | ATTAA others(3941): Show |
chr1 | 16119337 | 16161069 |
| a0001c0034t0001 | 0/0 | 3946 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | ATTAA others(3941): Show |
chr1 | 16119337 | 16161069 |
| a0001c0036t0001 | 0/0 | 3946 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | ATTAA others(3941): Show |
chr1 | 16119337 | 16161069 |
| a0002c0008t0003 | 0/0 | 3946 | 7 | 7 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | ATTAA others(3941): Show |
chr1 | 16119337 | 16161069 |
| a0002c0035t0003 | 0/0 | 3946 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | ATTAA others(3941): Show |
chr1 | 16119337 | 16161069 |
| a0003c0007t0001 | 0/0 | 3946 | 6 | 0 | 6 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | ATTAA others(3941): Show |
chr1 | 16119337 | 16161069 |
| a0003c0007t0005 | 0/0 | 3946 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | ATTAA others(3941): Show |
chr1 | 16119337 | 16161069 |
| a0004c0011t0001 | 0/0 | 3946 | 3 | 3 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | ATTAA others(3941): Show |
chr1 | 16119337 | 16161069 |
| a0005c0017t0001 | 0/0 | 3946 | 2 | 0 | 1 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | ATTAA others(3941): Show |
chr1 | 16119337 | 16161069 |
| a0006c0013t0003 | 0/0 | 3946 | 2 | 2 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | ATTAA others(3941): Show |
chr1 | 16119337 | 16161069 |
| a0007c0022t0001 | 0/0 | 3946 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | ATTAA others(3941): Show |
chr1 | 16119337 | 16161069 |
| a0008c0020t0001 | 0/0 | 3946 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | ATTAA others(3941): Show |
chr1 | 16119337 | 16161069 |
| a0009c0029t0001 | 0/0 | 3946 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | ATTAA others(3941): Show |
chr1 | 16119337 | 16161069 |
| a0010c0021t0001 | 0/0 | 3946 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | ATTAA others(3941): Show |
chr1 | 16119337 | 16161069 |
| a0011c0028t0001 | 0/0 | 3946 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA2_chr1_16119337_16161069 | EPHA2 | ATTAA others(3941): Show |
chr1 | 16119337 | 16161069 |
| a0012c0019t0001 | 0/0 | 3946 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | ATTAA others(3941): Show |
chr1 | 16119337 | 16161069 |
| a0013c0025t0001 | 0/0 | 3946 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA2_chr1_16119337_16161069 | EPHA2 | ATTAA others(3941): Show |
chr1 | 16119337 | 16161069 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 16 | 1 | 6 | 4 | 0 | 5 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0001t0001g0003 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0001t0001g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0001t0001g0010 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0001t0001g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0001t0001g0012 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0001t0001g0019 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0001t0001g0020 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0001t0001g0023 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0001t0002g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0001t0002g0097 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0001t0006g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0002t0001g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0002t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0002t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0002t0001g0039 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0002t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0002t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0002t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0002t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0002t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0002t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0002t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0002t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0002t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0002t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0002t0002g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0002t0002g0029 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0002t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0002t0002g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0002t0002g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0002t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0002t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0002t0002g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0002t0004g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0002t0004g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0002t0004g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0003t0001g0007 | 0/0 | 4 | 0 | 1 | 2 | 1 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0003t0001g0013 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0003t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0003t0001g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0003t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0003t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0003t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0003t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0003t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0003t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0003t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0003t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0003t0001g0166 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0003t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0003t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0003t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0003t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0003t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0003t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0003t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0003t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0003t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0003t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0004t0001g0009 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0004t0001g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0004t0001g0024 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0004t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0004t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0004t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0004t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0004t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0004t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0004t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0004t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0004t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0004t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0004t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0004t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0004t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0004t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0004t0002g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0004t0002g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0004t0002g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0004t0002g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0005t0001g0002 | 0/0 | 7 | 1 | 2 | 0 | 2 | 2 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0005t0001g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0005t0001g0016 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0005t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0005t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0005t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0005t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0005t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0005t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0005t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0005t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0005t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0005t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0005t0007g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0006t0001g0004 | 0/0 | 5 | 0 | 0 | 1 | 2 | 2 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0006t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0006t0001g0036 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0006t0001g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0006t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0006t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0006t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0006t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0006t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0006t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0006t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0006t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0006t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0009t0001g0008 | 0/0 | 4 | 1 | 3 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0009t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0009t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0010t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0010t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0010t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0010t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0012t0001g0017 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0014t0001g0034 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0015t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0015t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0016t0001g0033 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0018t0002g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0023t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0024t0003g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0026t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0027t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0030t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0031t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0032t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0033t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0034t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0001c0036t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0002c0008t0003g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0002c0008t0003g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0002c0008t0003g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0002c0008t0003g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0002c0008t0003g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0002c0035t0003g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0003c0007t0001g0005 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0003c0007t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0003c0007t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0003c0007t0005g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0004c0011t0001g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0004c0011t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0005c0017t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0005c0017t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0006c0013t0003g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0006c0013t0003g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0007c0022t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0008c0020t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0009c0029t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0010c0021t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0011c0028t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0012c0019t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| a0013c0025t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0003 | t0001 | g0007 | EUR | GBR | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG00099 | hp2 | a0001 | c0006 | t0001 | g0036 | EUR | GBR | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0018 | EUR | FIN | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0216 | EUR | FIN | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG00323 | hp1 | a0001 | c0006 | t0001 | g0004 | EUR | FIN | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG00323 | hp2 | a0001 | c0002 | t0001 | g0039 | EUR | FIN | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | CHS | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | CHS | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | CHS | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | CHS | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | CHS | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG00609 | hp2 | a0001 | c0002 | t0004 | g0094 | EAS | CHS | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG00621 | hp1 | a0001 | c0002 | t0004 | g0180 | EAS | CHS | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | CHS | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG00639 | hp2 | a0001 | c0009 | t0001 | g0196 | AMR | PUR | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG00642 | hp2 | a0001 | c0004 | t0001 | g0047 | AMR | PUR | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG00673 | hp1 | a0005 | c0017 | t0001 | g0063 | EAS | CHS | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG00673 | hp2 | a0001 | c0001 | t0006 | g0065 | EAS | CHS | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG00733 | hp1 | a0001 | c0006 | t0001 | g0132 | AMR | PUR | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG00733 | hp2 | a0001 | c0002 | t0002 | g0092 | AMR | PUR | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG00735 | hp1 | a0001 | c0002 | t0001 | g0039 | AMR | PUR | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG00735 | hp2 | a0007 | c0022 | t0001 | g0218 | AMR | PUR | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG00738 | hp2 | a0001 | c0009 | t0001 | g0008 | AMR | PUR | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG00741 | hp1 | a0008 | c0020 | t0001 | g0185 | AMR | PUR | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0072 | AMR | PUR | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG01069 | hp1 | a0001 | c0002 | t0001 | g0028 | AMR | PUR | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG01069 | hp2 | a0001 | c0006 | t0001 | g0088 | AMR | PUR | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG01071 | hp1 | a0001 | c0005 | t0001 | g0016 | AMR | PUR | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG01071 | hp2 | a0001 | c0002 | t0001 | g0028 | AMR | PUR | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG01074 | hp1 | a0001 | c0002 | t0002 | g0029 | AMR | PUR | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG01081 | hp1 | a0003 | c0007 | t0005 | g0045 | AMR | PUR | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0204 | AMR | PUR | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG01109 | hp1 | a0001 | c0003 | t0001 | g0173 | AMR | PUR | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG01109 | hp2 | a0001 | c0012 | t0001 | g0017 | AMR | PUR | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG01167 | hp1 | a0001 | c0002 | t0001 | g0202 | AMR | PUR | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG01168 | hp2 | a0001 | c0006 | t0001 | g0037 | AMR | PUR | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG01169 | hp2 | a0001 | c0006 | t0001 | g0037 | AMR | PUR | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG01192 | hp1 | a0005 | c0017 | t0001 | g0175 | AMR | PUR | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG01192 | hp2 | a0001 | c0005 | t0001 | g0130 | AMR | PUR | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG01243 | hp2 | a0001 | c0034 | t0001 | g0217 | AMR | PUR | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG01256 | hp2 | a0001 | c0003 | t0001 | g0007 | AMR | CLM | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG01257 | hp2 | a0001 | c0009 | t0001 | g0008 | AMR | CLM | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG01261 | hp2 | a0001 | c0014 | t0001 | g0034 | AMR | CLM | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0176 | AMR | CLM | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG01361 | hp2 | a0003 | c0007 | t0001 | g0005 | AMR | CLM | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG01433 | hp1 | a0001 | c0002 | t0002 | g0093 | AMR | CLM | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG01433 | hp2 | a0003 | c0007 | t0001 | g0005 | AMR | CLM | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG01496 | hp2 | a0001 | c0009 | t0001 | g0008 | AMR | CLM | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG01515 | hp1 | a0001 | c0016 | t0001 | g0033 | EUR | IBS | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG01515 | hp2 | a0001 | c0005 | t0001 | g0128 | EUR | IBS | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG01516 | hp1 | a0001 | c0031 | t0001 | g0135 | EUR | IBS | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG01516 | hp2 | a0001 | c0005 | t0001 | g0002 | EUR | IBS | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG01517 | hp1 | a0001 | c0016 | t0001 | g0033 | EUR | IBS | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG01517 | hp2 | a0001 | c0005 | t0001 | g0002 | EUR | IBS | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG01884 | hp1 | a0001 | c0005 | t0001 | g0015 | AFR | ACB | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG01884 | hp2 | a0001 | c0004 | t0001 | g0214 | AFR | ACB | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG01891 | hp1 | a0009 | c0029 | t0001 | g0114 | AFR | ACB | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG01891 | hp2 | a0001 | c0004 | t0001 | g0009 | AFR | ACB | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG01928 | hp2 | a0001 | c0030 | t0001 | g0136 | AMR | PEL | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG01934 | hp1 | a0001 | c0003 | t0001 | g0167 | AMR | PEL | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG01934 | hp2 | a0001 | c0002 | t0001 | g0148 | AMR | PEL | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG01943 | hp2 | a0003 | c0007 | t0001 | g0119 | AMR | PEL | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG01952 | hp2 | a0001 | c0003 | t0001 | g0177 | AMR | PEL | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG01975 | hp1 | a0001 | c0010 | t0001 | g0070 | AMR | PEL | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG01975 | hp2 | a0001 | c0005 | t0001 | g0002 | AMR | PEL | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG01978 | hp1 | a0003 | c0007 | t0001 | g0005 | AMR | PEL | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG01978 | hp2 | a0001 | c0005 | t0001 | g0002 | AMR | PEL | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG01993 | hp1 | a0003 | c0007 | t0001 | g0125 | AMR | PEL | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | PEL | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG02015 | hp2 | a0001 | c0002 | t0002 | g0049 | EAS | KHV | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | KHV | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG02027 | hp2 | a0001 | c0003 | t0001 | g0041 | EAS | KHV | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | KHV | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | KHV | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | KHV | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | KHV | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG02083 | hp1 | a0010 | c0021 | t0001 | g0186 | EAS | KHV | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG02083 | hp2 | a0001 | c0002 | t0001 | g0030 | EAS | KHV | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG02129 | hp1 | a0001 | c0023 | t0002 | g0124 | EAS | KHV | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG02135 | hp2 | a0001 | c0003 | t0001 | g0193 | EAS | KHV | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG02145 | hp1 | a0001 | c0024 | t0003 | g0086 | AFR | ACB | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG02145 | hp2 | a0001 | c0027 | t0001 | g0199 | AFR | ACB | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG02165 | hp1 | a0001 | c0002 | t0002 | g0104 | EAS | CDX | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG02257 | hp1 | a0004 | c0011 | t0001 | g0209 | AFR | ACB | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG02257 | hp2 | a0001 | c0004 | t0001 | g0024 | AFR | ACB | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG02258 | hp1 | a0001 | c0002 | t0001 | g0156 | AFR | ACB | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG02258 | hp2 | a0001 | c0003 | t0001 | g0171 | AFR | ACB | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG02293 | hp2 | a0003 | c0007 | t0001 | g0005 | AMR | PEL | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG02300 | hp1 | a0001 | c0015 | t0001 | g0201 | AMR | PEL | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG02300 | hp2 | a0001 | c0006 | t0001 | g0036 | AMR | PEL | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | ACB | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | ACB | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | KHV | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | KHV | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0212 | AFR | GWD | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG02572 | hp2 | a0002 | c0008 | t0003 | g0014 | AFR | GWD | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0052 | SAS | PJL | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0142 | SAS | PJL | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG02615 | hp1 | a0001 | c0005 | t0001 | g0089 | AFR | GWD | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG02615 | hp2 | a0001 | c0012 | t0001 | g0017 | AFR | GWD | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG02622 | hp1 | a0001 | c0004 | t0001 | g0024 | AFR | GWD | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG02622 | hp2 | a0001 | c0002 | t0002 | g0105 | AFR | GWD | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG02630 | hp1 | a0001 | c0015 | t0001 | g0182 | AFR | GWD | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG02630 | hp2 | a0001 | c0004 | t0001 | g0213 | AFR | GWD | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0162 | SAS | PJL | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG02683 | hp2 | a0001 | c0005 | t0001 | g0129 | SAS | PJL | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG02698 | hp1 | a0001 | c0004 | t0001 | g0161 | SAS | PJL | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG02698 | hp2 | a0011 | c0028 | t0001 | g0117 | SAS | PJL | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG02717 | hp1 | a0002 | c0008 | t0003 | g0112 | AFR | GWD | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG02717 | hp2 | a0001 | c0003 | t0001 | g0195 | AFR | GWD | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG02723 | hp1 | a0001 | c0004 | t0002 | g0032 | AFR | GWD | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG02723 | hp2 | a0001 | c0004 | t0001 | g0205 | AFR | GWD | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG02735 | hp1 | a0001 | c0006 | t0001 | g0004 | SAS | PJL | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG02735 | hp2 | a0001 | c0006 | t0001 | g0118 | SAS | PJL | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG02738 | hp1 | a0001 | c0003 | t0001 | g0013 | SAS | PJL | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG02738 | hp2 | a0001 | c0005 | t0001 | g0127 | SAS | PJL | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0207 | AFR | GWD | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG02809 | hp2 | a0001 | c0004 | t0001 | g0140 | AFR | GWD | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG02818 | hp1 | a0001 | c0018 | t0002 | g0043 | AFR | GWD | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG02818 | hp2 | a0001 | c0005 | t0001 | g0016 | AFR | GWD | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG02886 | hp1 | a0001 | c0002 | t0001 | g0031 | AFR | GWD | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG02886 | hp2 | a0001 | c0002 | t0001 | g0210 | AFR | GWD | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG02895 | hp1 | a0002 | c0008 | t0003 | g0215 | AFR | GWD | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG02895 | hp2 | a0001 | c0005 | t0001 | g0133 | AFR | GWD | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG02896 | hp1 | a0001 | c0004 | t0001 | g0021 | AFR | GWD | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG02896 | hp2 | a0001 | c0003 | t0001 | g0155 | AFR | GWD | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG02897 | hp1 | a0002 | c0008 | t0003 | g0206 | AFR | GWD | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG02897 | hp2 | a0001 | c0004 | t0001 | g0021 | AFR | GWD | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG02922 | hp1 | a0001 | c0004 | t0002 | g0108 | AFR | ESN | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG02922 | hp2 | a0001 | c0036 | t0001 | g0110 | AFR | ESN | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG02965 | hp1 | a0001 | c0005 | t0001 | g0137 | AFR | ESN | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG02965 | hp2 | a0001 | c0003 | t0001 | g0042 | AFR | ESN | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG02970 | hp1 | a0001 | c0002 | t0001 | g0050 | AFR | ESN | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG02970 | hp2 | a0002 | c0008 | t0003 | g0113 | AFR | ESN | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG02976 | hp1 | a0001 | c0012 | t0001 | g0017 | AFR | ESN | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG02976 | hp2 | a0001 | c0032 | t0001 | g0048 | AFR | ESN | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG03017 | hp1 | a0001 | c0006 | t0001 | g0087 | SAS | PJL | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG03017 | hp2 | a0001 | c0003 | t0001 | g0158 | SAS | PJL | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG03041 | hp1 | a0002 | c0008 | t0003 | g0014 | AFR | GWD | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG03041 | hp2 | a0001 | c0009 | t0001 | g0008 | AFR | GWD | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG03098 | hp1 | a0001 | c0005 | t0001 | g0016 | AFR | MSL | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG03098 | hp2 | a0001 | c0003 | t0001 | g0042 | AFR | MSL | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG03130 | hp1 | a0012 | c0019 | t0001 | g0203 | AFR | ESN | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG03130 | hp2 | a0006 | c0013 | t0003 | g0123 | AFR | ESN | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | ESN | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG03139 | hp2 | a0001 | c0004 | t0001 | g0021 | AFR | ESN | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG03195 | hp1 | a0001 | c0004 | t0001 | g0211 | AFR | ESN | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG03195 | hp2 | a0001 | c0005 | t0001 | g0139 | AFR | ESN | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG03209 | hp1 | a0001 | c0004 | t0002 | g0032 | AFR | MSL | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG03209 | hp2 | a0001 | c0002 | t0001 | g0083 | AFR | MSL | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG03225 | hp1 | a0002 | c0035 | t0003 | g0200 | AFR | MSL | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0069 | SAS | PJL | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG03239 | hp2 | a0001 | c0006 | t0001 | g0004 | SAS | PJL | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG03453 | hp1 | a0001 | c0004 | t0001 | g0154 | AFR | MSL | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG03453 | hp2 | a0001 | c0002 | t0001 | g0080 | AFR | MSL | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG03486 | hp1 | a0001 | c0018 | t0002 | g0043 | AFR | MSL | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG03486 | hp2 | a0001 | c0002 | t0001 | g0183 | AFR | MSL | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0090 | SAS | PJL | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG03490 | hp2 | a0001 | c0005 | t0001 | g0002 | SAS | PJL | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG03491 | hp2 | a0001 | c0006 | t0001 | g0121 | SAS | PJL | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG03492 | hp1 | a0001 | c0005 | t0001 | g0002 | SAS | PJL | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG03540 | hp1 | a0002 | c0008 | t0003 | g0014 | AFR | GWD | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG03540 | hp2 | a0001 | c0004 | t0002 | g0107 | AFR | GWD | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG03579 | hp1 | a0001 | c0002 | t0001 | g0031 | AFR | MSL | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG03579 | hp2 | a0004 | c0011 | t0001 | g0044 | AFR | MSL | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG03654 | hp1 | a0001 | c0033 | t0001 | g0099 | SAS | PJL | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG03654 | hp2 | a0001 | c0010 | t0001 | g0163 | SAS | PJL | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0066 | SAS | PJL | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0178 | SAS | PJL | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG03704 | hp1 | a0001 | c0003 | t0001 | g0013 | SAS | PJL | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG03704 | hp2 | a0001 | c0003 | t0001 | g0013 | SAS | PJL | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0153 | SAS | PJL | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0144 | SAS | PJL | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG03831 | hp1 | a0001 | c0004 | t0001 | g0168 | SAS | BEB | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG03831 | hp2 | a0001 | c0003 | t0001 | g0160 | SAS | BEB | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG03834 | hp1 | a0001 | c0006 | t0001 | g0134 | SAS | BEB | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0079 | SAS | BEB | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG03942 | hp1 | a0001 | c0003 | t0001 | g0159 | SAS | BEB | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG03942 | hp2 | a0001 | c0002 | t0001 | g0189 | SAS | BEB | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0058 | SAS | STU | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0174 | SAS | BEB | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG04204 | hp1 | a0001 | c0006 | t0001 | g0116 | SAS | STU | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0188 | SAS | STU | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| NA18522 | hp1 | a0001 | c0005 | t0001 | g0015 | AFR | YRI | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| NA18522 | hp2 | a0004 | c0011 | t0001 | g0044 | AFR | YRI | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| NA18747 | hp1 | a0001 | c0002 | t0001 | g0091 | EAS | CHB | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | CHB | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| NA18906 | hp1 | a0001 | c0004 | t0001 | g0009 | AFR | YRI | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| NA18906 | hp2 | a0001 | c0003 | t0001 | g0172 | AFR | YRI | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| NA18944 | hp1 | a0001 | c0002 | t0004 | g0098 | EAS | JPT | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| NA18951 | hp2 | a0001 | c0003 | t0001 | g0007 | EAS | JPT | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| NA18954 | hp2 | a0001 | c0003 | t0001 | g0007 | EAS | JPT | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0190 | EAS | JPT | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| NA18961 | hp2 | a0001 | c0002 | t0002 | g0026 | EAS | JPT | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| NA18965 | hp1 | a0001 | c0006 | t0001 | g0035 | EAS | JPT | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| NA18973 | hp1 | a0001 | c0003 | t0001 | g0157 | EAS | JPT | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| NA18974 | hp1 | a0001 | c0003 | t0001 | g0041 | EAS | JPT | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0101 | EAS | JPT | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| NA18980 | hp1 | a0001 | c0002 | t0002 | g0103 | EAS | JPT | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| NA18985 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| NA18986 | hp1 | a0001 | c0003 | t0001 | g0169 | EAS | JPT | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| NA18990 | hp1 | a0001 | c0003 | t0001 | g0170 | EAS | JPT | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| NA18998 | hp2 | a0001 | c0006 | t0001 | g0004 | EAS | JPT | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| NA18999 | hp2 | a0001 | c0006 | t0001 | g0187 | EAS | JPT | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| NA19001 | hp1 | a0001 | c0003 | t0001 | g0165 | EAS | JPT | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| NA19001 | hp2 | a0001 | c0006 | t0001 | g0115 | EAS | JPT | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| NA19004 | hp2 | a0001 | c0006 | t0001 | g0035 | EAS | JPT | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| NA19005 | hp2 | a0001 | c0002 | t0001 | g0030 | EAS | JPT | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| NA19007 | hp1 | a0001 | c0003 | t0001 | g0194 | EAS | JPT | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| NA19011 | hp2 | a0001 | c0014 | t0001 | g0034 | EAS | JPT | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| NA19012 | hp1 | a0001 | c0003 | t0001 | g0164 | EAS | JPT | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| NA19030 | hp1 | a0001 | c0026 | t0001 | g0138 | AFR | LWK | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| NA19030 | hp2 | a0001 | c0004 | t0001 | g0009 | AFR | LWK | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| NA19043 | hp1 | a0001 | c0005 | t0001 | g0002 | AFR | LWK | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| NA19043 | hp2 | a0001 | c0004 | t0001 | g0184 | AFR | LWK | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| NA19065 | hp1 | a0001 | c0010 | t0001 | g0064 | EAS | JPT | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| NA19080 | hp2 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| NA19088 | hp2 | a0001 | c0002 | t0002 | g0026 | EAS | JPT | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| NA19240 | hp1 | a0001 | c0004 | t0001 | g0046 | AFR | YRI | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | YRI | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| NA20129 | hp1 | a0001 | c0004 | t0001 | g0009 | AFR | ASW | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| NA20129 | hp2 | a0001 | c0010 | t0001 | g0151 | AFR | ASW | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0061 | EUR | TSI | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| NA20752 | hp2 | a0001 | c0003 | t0001 | g0145 | EUR | TSI | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0146 | EUR | TSI | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| NA20805 | hp2 | a0001 | c0006 | t0001 | g0004 | EUR | TSI | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| NA20905 | hp1 | a0013 | c0025 | t0001 | g0120 | SAS | GIH | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0059 | AMR | CLM | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0095 | AMR | CLM | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG02109 | hp1 | a0001 | c0005 | t0001 | g0015 | AFR | ACB | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG02109 | hp2 | a0001 | c0004 | t0001 | g0208 | AFR | ACB | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG02486 | hp1 | a0001 | c0002 | t0001 | g0084 | AFR | ACB | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG02486 | hp2 | a0001 | c0005 | t0001 | g0131 | AFR | ACB | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG02559 | hp1 | a0001 | c0005 | t0007 | g0122 | AFR | ACB | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG02559 | hp2 | a0001 | c0009 | t0001 | g0197 | AFR | ACB | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG03471 | hp1 | a0001 | c0002 | t0001 | g0082 | AFR | MSL | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG03471 | hp2 | a0001 | c0004 | t0002 | g0109 | AFR | MSL | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG06807 | hp1 | a0001 | c0005 | t0001 | g0126 | AFR | USA | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| HG06807 | hp2 | a0006 | c0013 | t0003 | g0081 | AFR | USA | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| NA20300 | hp1 | a0001 | c0004 | t0001 | g0106 | AFR | USA | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| NA20300 | hp2 | a0001 | c0002 | t0002 | g0029 | AFR | USA | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| NA21309 | hp1 | a0001 | c0004 | t0001 | g0198 | AFR | LWK | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| NA21309 | hp2 | a0001 | c0004 | t0001 | g0024 | AFR | LWK | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| homoSapiens | chm13v2 | a0001 | c0003 | t0001 | g0166 | REF | REF | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0097 | REF | REF | EPHA2_chr1_16119337_16161069 | EPHA2 | chr1 | 16119337 | 16161069 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:16125271 | C | T | 1 | a0007 | 1 | HG00735.hp2 | missense_variant | MODERATE | c.2875G>A | p.Ala959Thr | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 17/17 | 3012/3946 | 2875/2931 | 959/976 | chr1 | 16125271 | |||
| chr1:16131741 | A | C | 1 | a0013 | 1 | NA20905.hp1 | missense_variant | MODERATE | c.2455T>G | p.Trp819Gly | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 14/17 | 2592/3946 | 2455/2931 | 819/976 | chr1 | 16131741 | |||
| chr1:16133341 | A | G | 2 | a0002 a0006 |
10 | HG02572.hp2 HG02717.hp1 HG02895.hp1 others(7): Show |
missense_variant | MODERATE | c.1892T>C | p.Met631Thr | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 11/17 | 2029/3946 | 1892/2931 | 631/976 | chr1 | 16133341 | |||
| chr1:16134529 | C | T | 1 | a0004 | 3 | HG02257.hp1 HG03579.hp2 NA18522.hp2 |
missense_variant | MODERATE | c.1621G>A | p.Val541Met | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 8/17 | 1758/3946 | 1621/2931 | 541/976 | chr1 | 16134529 | |||
| chr1:16135086 | G | A | 1 | a0005 | 2 | HG00673.hp1 HG01192.hp1 |
missense_variant | MODERATE | c.1532C>T | p.Thr511Met | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 7/17 | 1669/3946 | 1532/2931 | 511/976 | chr1 | 16135086 | |||
| chr1:16135132 | C | T | 1 | a0006 | 2 | HG03130.hp2 HG06807.hp2 |
missense_variant | MODERATE | c.1486G>A | p.Asp496Asn | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 7/17 | 1623/3946 | 1486/2931 | 496/976 | chr1 | 16135132 | |||
| chr1:16135176 | C | G | 1 | a0010 | 1 | HG02083.hp1 | missense_variant | MODERATE | c.1442G>C | p.Ser481Thr | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 7/17 | 1579/3946 | 1442/2931 | 481/976 | chr1 | 16135176 | |||
| chr1:16137994 | C | T | 2 | a0003 a0008 |
8 | HG00741.hp1 HG01081.hp1 HG01361.hp2 others(5): Show |
missense_variant | MODERATE | c.1171G>A | p.Gly391Arg | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/17 | 1308/3946 | 1171/2931 | 391/976 | chr1 | 16137994 | |||
| chr1:16138119 | G | A | 1 | a0011 | 1 | HG02698.hp2 | missense_variant | MODERATE | c.1046C>T | p.Thr349Met | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/17 | 1183/3946 | 1046/2931 | 349/976 | chr1 | 16138119 | |||
| chr1:16138310 | C | T | 1 | a0008 | 1 | HG00741.hp1 | missense_variant | MODERATE | c.944G>A | p.Arg315Gln | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 4/17 | 1081/3946 | 944/2931 | 315/976 | chr1 | 16138310 | |||
| chr1:16148506 | T | C | 1 | a0009 | 1 | HG01891.hp1 | missense_variant | MODERATE | c.695A>G | p.Asp232Gly | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/17 | 832/3946 | 695/2931 | 232/976 | chr1 | 16148506 | |||
| chr1:16148708 | C | T | 1 | a0012 | 1 | HG03130.hp1 | missense_variant | MODERATE | c.493G>A | p.Val165Met | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/17 | 630/3946 | 493/2931 | 165/976 | chr1 | 16148708 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:16125227 | C | T | 1 | a0001c0009 | 6 | HG00639.hp2 HG00738.hp2 HG01257.hp2 others(3): Show |
synonymous_variant | LOW | c.2919G>A | p.Gly973Gly | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 17/17 | 3056/3946 | 2919/2931 | 973/976 | chr1 | 16125227 | |||
| chr1:16125272 | G | A | 15 | a0001c0003 a0001c0006 a0001c0010 others(12): Show |
74 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(71): Show |
synonymous_variant | LOW | c.2874C>T | p.Ile958Ile | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 17/17 | 3011/3946 | 2874/2931 | 958/976 | chr1 | 16125272 | |||
| chr1:16130303 | G | A | 1 | a0001c0032 | 1 | HG02976.hp2 | synonymous_variant | LOW | c.2592C>T | p.Phe864Phe | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 15/17 | 2729/3946 | 2592/2931 | 864/976 | chr1 | 16130303 | |||
| chr1:16130381 | T | C | 4 | a0001c0024 a0002c0008 a0002c0035 others(1): Show |
11 | HG02145.hp1 HG02572.hp2 HG02717.hp1 others(8): Show |
synonymous_variant | LOW | c.2514A>G | p.Thr838Thr | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 15/17 | 2651/3946 | 2514/2931 | 838/976 | chr1 | 16130381 | |||
| chr1:16133199 | T | C | 7 | a0001c0012 a0001c0024 a0001c0027 others(4): Show |
16 | HG01109.hp2 HG02145.hp1 HG02145.hp2 others(13): Show |
synonymous_variant | LOW | c.2034A>G | p.Leu678Leu | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 11/17 | 2171/3946 | 2034/2931 | 678/976 | chr1 | 16133199 | |||
| chr1:16133250 | G | A | 12 | a0001c0003 a0001c0004 a0001c0012 others(9): Show |
74 | HG00099.hp1 HG00642.hp2 HG01109.hp1 others(71): Show |
synonymous_variant | LOW | c.1983C>T | p.Leu661Leu | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 11/17 | 2120/3946 | 1983/2931 | 661/976 | chr1 | 16133250 | |||
| chr1:16133292 | C | A | 1 | a0001c0016 | 2 | HG01515.hp1 HG01517.hp1 |
synonymous_variant | LOW | c.1941G>T | p.Thr647Thr | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 11/17 | 2078/3946 | 1941/2931 | 647/976 | chr1 | 16133292 | |||
| chr1:16135106 | C | A | 4 | a0001c0036 a0002c0008 a0002c0035 others(1): Show |
11 | HG02572.hp2 HG02717.hp1 HG02895.hp1 others(8): Show |
synonymous_variant | LOW | c.1512G>T | p.Leu504Leu | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 7/17 | 1649/3946 | 1512/2931 | 504/976 | chr1 | 16135106 | |||
| chr1:16138178 | G | A | 19 | a0001c0002 a0001c0005 a0001c0006 others(16): Show |
108 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(105): Show |
synonymous_variant | LOW | c.987C>T | p.Pro329Pro | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/17 | 1124/3946 | 987/2931 | 329/976 | chr1 | 16138178 | |||
| chr1:16148553 | G | A | 2 | a0001c0030 a0001c0031 |
2 | HG01516.hp1 HG01928.hp2 |
synonymous_variant | LOW | c.648C>T | p.Ala216Ala | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/17 | 785/3946 | 648/2931 | 216/976 | chr1 | 16148553 | |||
| chr1:16148628 | C | T | 20 | a0001c0005 a0001c0006 a0001c0009 others(17): Show |
77 | HG00099.hp2 HG00323.hp1 HG00639.hp2 others(74): Show |
synonymous_variant | LOW | c.573G>A | p.Leu191Leu | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/17 | 710/3946 | 573/2931 | 191/976 | chr1 | 16148628 | |||
| chr1:16148631 | C | T | 20 | a0001c0005 a0001c0006 a0001c0009 others(17): Show |
77 | HG00099.hp2 HG00323.hp1 HG00639.hp2 others(74): Show |
synonymous_variant | LOW | c.570G>A | p.Ala190Ala | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/17 | 707/3946 | 570/2931 | 190/976 | chr1 | 16148631 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:16124473 | A | T | 4 | a0001c0024t0003 a0002c0008t0003 a0002c0035t0003 others(1): Show |
11 | HG02145.hp1 HG02572.hp2 HG02717.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*742T>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 17/17 | 742 | chr1 | 16124473 | ||||||
| chr1:16124501 | C | T | 4 | a0001c0024t0003 a0002c0008t0003 a0002c0035t0003 others(1): Show |
11 | HG02145.hp1 HG02572.hp2 HG02717.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*714G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 17/17 | 714 | chr1 | 16124501 | ||||||
| chr1:16124556 | A | T | 1 | a0001c0001t0006 | 1 | HG00673.hp2 | 3_prime_UTR_variant | MODIFIER | c.*659T>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 17/17 | 659 | chr1 | 16124556 | ||||||
| chr1:16124705 | C | T | 1 | a0001c0002t0004 | 3 | HG00609.hp2 HG00621.hp1 NA18944.hp1 |
3_prime_UTR_variant | MODIFIER | c.*510G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 17/17 | 510 | chr1 | 16124705 | ||||||
| chr1:16124772 | A | G | 4 | a0001c0024t0003 a0002c0008t0003 a0002c0035t0003 others(1): Show |
11 | HG02145.hp1 HG02572.hp2 HG02717.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*443T>C | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 17/17 | 443 | chr1 | 16124772 | ||||||
| chr1:16124888 | G | C | 1 | a0001c0005t0007 | 1 | HG02559.hp1 | 3_prime_UTR_variant | MODIFIER | c.*327C>G | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 17/17 | 327 | chr1 | 16124888 | ||||||
| chr1:16124918 | C | T | 37 | a0001c0001t0001 a0001c0001t0006 a0001c0002t0001 others(34): Show |
279 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(276): Show |
3_prime_UTR_variant | MODIFIER | c.*297G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 17/17 | 297 | chr1 | 16124918 | ||||||
| chr1:16125049 | C | T | 4 | a0001c0024t0003 a0002c0008t0003 a0002c0035t0003 others(1): Show |
11 | HG02145.hp1 HG02572.hp2 HG02717.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*166G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 17/17 | 166 | chr1 | 16125049 | ||||||
| chr1:16155935 | C | T | 1 | a0003c0007t0005 | 1 | HG01081.hp1 | 5_prime_UTR_variant | MODIFIER | c.-3G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 1/17 | 3 | chr1 | 16155935 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:16125376 | G | A | 2 | a0001c0001t0001g0053 a0001c0001t0001g0102 |
2 | NA18957.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.2826-56C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 16/16 | chr1 | 16125376 | |||||||
| chr1:16125381 | G | A | 13 | a0001c0001t0001g0085 a0001c0001t0001g0162 a0001c0001t0001g0178 others(10): Show |
14 | HG01069.hp1 HG01071.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.2826-61C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 16/16 | chr1 | 16125381 | |||||||
| chr1:16125526 | G | A | 1 | a0001c0004t0001g0106 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2826-206C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 16/16 | chr1 | 16125526 | |||||||
| chr1:16125561 | C | T | 1 | a0001c0002t0002g0103 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.2826-241G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 16/16 | chr1 | 16125561 | |||||||
| chr1:16125562 | G | A | 3 | a0001c0004t0001g0046 a0001c0004t0001g0047 a0007c0022t0001g0218 |
3 | HG00642.hp2 HG00735.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2826-242C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 16/16 | chr1 | 16125562 | |||||||
| chr1:16125706 | A | G | 104 | a0001c0001t0001g0085 a0001c0001t0001g0100 a0001c0001t0001g0111 others(101): Show |
137 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.2826-386T>C | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 16/16 | chr1 | 16125706 | |||||||
| chr1:16125799 | C | T | 3 | a0001c0001t0001g0090 a0001c0001t0001g0153 a0005c0017t0001g0175 |
3 | HG01192.hp1 HG03490.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.2826-479G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 16/16 | chr1 | 16125799 | |||||||
| chr1:16125964 | G | A | 1 | a0001c0004t0001g0198 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2826-644C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 16/16 | chr1 | 16125964 | |||||||
| chr1:16126047 | C | T | 9 | a0001c0024t0003g0086 a0002c0008t0003g0014 a0002c0008t0003g0112 others(6): Show |
11 | HG02145.hp1 HG02572.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.2826-727G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 16/16 | chr1 | 16126047 | |||||||
| chr1:16126048 | G | A | 2 | a0001c0012t0001g0017 a0001c0027t0001g0199 |
4 | HG01109.hp2 HG02145.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.2826-728C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 16/16 | chr1 | 16126048 | |||||||
| chr1:16126115 | G | T | 9 | a0001c0024t0003g0086 a0002c0008t0003g0014 a0002c0008t0003g0112 others(6): Show |
11 | HG02145.hp1 HG02572.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.2826-795C>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 16/16 | chr1 | 16126115 | |||||||
| chr1:16126163 | G | T | 6 | a0001c0024t0003g0086 a0002c0008t0003g0112 a0002c0008t0003g0113 others(3): Show |
6 | HG02145.hp1 HG02717.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.2826-843C>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 16/16 | chr1 | 16126163 | |||||||
| chr1:16126260 | G | A | 10 | a0001c0004t0001g0106 a0001c0024t0003g0086 a0002c0008t0003g0014 others(7): Show |
12 | HG02145.hp1 HG02572.hp2 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.2826-940C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 16/16 | chr1 | 16126260 | |||||||
| chr1:16126341 | T | A | 1 | a0001c0006t0001g0132 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.2826-1021A>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 16/16 | chr1 | 16126341 | |||||||
| chr1:16126354 | C | T | 4 | a0001c0005t0001g0016 a0001c0005t0001g0126 a0001c0005t0001g0133 others(1): Show |
6 | HG01071.hp1 HG02818.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.2826-1034G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 16/16 | chr1 | 16126354 | |||||||
| chr1:16126474 | C | G | 1 | a0001c0001t0001g0111 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2826-1154G>C | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 16/16 | chr1 | 16126474 | |||||||
| chr1:16126503 | C | T | 87 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(84): Show |
142 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(139): Show |
intron_variant | MODIFIER | c.2826-1183G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 16/16 | chr1 | 16126503 | |||||||
| chr1:16126676 | C | T | 76 | a0001c0001t0001g0085 a0001c0001t0001g0162 a0001c0001t0001g0178 others(73): Show |
98 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.2826-1356G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 16/16 | chr1 | 16126676 | |||||||
| chr1:16126721 | T | A | 76 | a0001c0001t0001g0085 a0001c0001t0001g0162 a0001c0001t0001g0178 others(73): Show |
98 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.2826-1401A>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 16/16 | chr1 | 16126721 | |||||||
| chr1:16126796 | G | A | 1 | a0001c0004t0001g0208 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2826-1476C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 16/16 | chr1 | 16126796 | |||||||
| chr1:16126890 | C | A | 1 | a0001c0002t0002g0029 | 2 | HG01074.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2826-1570G>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 16/16 | chr1 | 16126890 | |||||||
| chr1:16127069 | G | A | 1 | a0001c0001t0001g0079 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2826-1749C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 16/16 | chr1 | 16127069 | |||||||
| chr1:16127120 | G | A | 1 | a0001c0024t0003g0086 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2826-1800C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 16/16 | chr1 | 16127120 | |||||||
| chr1:16127176 | C | T | 13 | a0001c0001t0001g0085 a0001c0001t0001g0162 a0001c0001t0001g0178 others(10): Show |
14 | HG01069.hp1 HG01071.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.2826-1856G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 16/16 | chr1 | 16127176 | |||||||
| chr1:16127343 | G | T | 1 | a0001c0005t0001g0128 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.2826-2023C>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 16/16 | chr1 | 16127343 | |||||||
| chr1:16127457 | G | T | 1 | a0001c0001t0001g0078 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.2825+1977C>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 16/16 | chr1 | 16127457 | |||||||
| chr1:16127467 | G | A | 9 | a0001c0024t0003g0086 a0002c0008t0003g0014 a0002c0008t0003g0112 others(6): Show |
11 | HG02145.hp1 HG02572.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.2825+1967C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 16/16 | chr1 | 16127467 | |||||||
| chr1:16128339 | G | C | 51 | a0001c0001t0001g0085 a0001c0001t0001g0162 a0001c0001t0001g0178 others(48): Show |
61 | HG00099.hp1 HG00642.hp2 HG01069.hp1 others(58): Show |
intron_variant | MODIFIER | c.2825+1095C>G | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 16/16 | chr1 | 16128339 | |||||||
| chr1:16128345 | G | A | 2 | a0001c0004t0001g0184 a0001c0004t0001g0198 |
2 | NA19043.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2825+1089C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 16/16 | chr1 | 16128345 | |||||||
| chr1:16128411 | G | A | 9 | a0001c0024t0003g0086 a0002c0008t0003g0014 a0002c0008t0003g0112 others(6): Show |
11 | HG02145.hp1 HG02572.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.2825+1023C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 16/16 | chr1 | 16128411 | |||||||
| chr1:16128557 | C | T | 112 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(109): Show |
179 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(176): Show |
intron_variant | MODIFIER | c.2825+877G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 16/16 | chr1 | 16128557 | |||||||
| chr1:16128647 | C | G | 9 | a0001c0024t0003g0086 a0002c0008t0003g0014 a0002c0008t0003g0112 others(6): Show |
11 | HG02145.hp1 HG02572.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.2825+787G>C | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 16/16 | chr1 | 16128647 | |||||||
| chr1:16128648 | T | C | 193 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(190): Show |
283 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(280): Show |
intron_variant | MODIFIER | c.2825+786A>G | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 16/16 | chr1 | 16128648 | |||||||
| chr1:16128840 | C | T | 9 | a0001c0024t0003g0086 a0002c0008t0003g0014 a0002c0008t0003g0112 others(6): Show |
11 | HG02145.hp1 HG02572.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.2825+594G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 16/16 | chr1 | 16128840 | |||||||
| chr1:16128879 | G | C | 1 | a0002c0008t0003g0113 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2825+555C>G | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 16/16 | chr1 | 16128879 | |||||||
| chr1:16128933 | T | A | 1 | a0001c0005t0001g0139 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2825+501A>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 16/16 | chr1 | 16128933 | |||||||
| chr1:16129022 | C | A | 9 | a0001c0024t0003g0086 a0002c0008t0003g0014 a0002c0008t0003g0112 others(6): Show |
11 | HG02145.hp1 HG02572.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.2825+412G>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 16/16 | chr1 | 16129022 | |||||||
| chr1:16129186 | G | T | 1 | a0007c0022t0001g0218 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.2825+248C>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 16/16 | chr1 | 16129186 | |||||||
| chr1:16129324 | A | G | 7 | a0001c0001t0001g0018 a0001c0001t0001g0090 a0001c0001t0001g0143 others(4): Show |
9 | HG00280.hp1 HG01074.hp2 HG01192.hp1 others(6): Show |
intron_variant | MODIFIER | c.2825+110T>C | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 16/16 | chr1 | 16129324 | |||||||
| chr1:16129364 | G | T | 1 | a0001c0001t0001g0111 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2825+70C>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 16/16 | chr1 | 16129364 | |||||||
| chr1:16129367 | G | A | 1 | a0001c0003t0001g0170 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.2825+67C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 16/16 | chr1 | 16129367 | |||||||
| chr1:16129660 | C | T | 2 | a0001c0004t0001g0184 a0001c0004t0001g0198 |
2 | NA19043.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2670-71G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 15/16 | chr1 | 16129660 | |||||||
| chr1:16129669 | G | T | 1 | a0001c0006t0001g0115 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.2670-80C>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 15/16 | chr1 | 16129669 | |||||||
| chr1:16129681 | G | A | 59 | a0001c0001t0001g0085 a0001c0001t0001g0162 a0001c0001t0001g0178 others(56): Show |
72 | HG00099.hp1 HG00642.hp2 HG01069.hp1 others(69): Show |
intron_variant | MODIFIER | c.2670-92C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 15/16 | chr1 | 16129681 | |||||||
| chr1:16129851 | G | A | 2 | a0001c0001t0001g0038 a0001c0001t0001g0073 |
3 | HG02523.hp2 NA18980.hp2 NA18997.hp1 |
intron_variant | MODIFIER | c.2670-262C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 15/16 | chr1 | 16129851 | |||||||
| chr1:16129934 | G | A | 1 | a0005c0017t0001g0175 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2669+292C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 15/16 | chr1 | 16129934 | |||||||
| chr1:16130071 | G | T | 1 | a0001c0004t0002g0107 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2669+155C>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 15/16 | chr1 | 16130071 | |||||||
| chr1:16130094 | A | T | 1 | a0001c0001t0001g0176 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.2669+132T>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 15/16 | chr1 | 16130094 | |||||||
| chr1:16130150 | G | A | 1 | a0001c0005t0001g0089 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2669+76C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 15/16 | chr1 | 16130150 | |||||||
| chr1:16130536 | G | A | 9 | a0001c0024t0003g0086 a0002c0008t0003g0014 a0002c0008t0003g0112 others(6): Show |
11 | HG02145.hp1 HG02572.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.2476-117C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 14/16 | chr1 | 16130536 | |||||||
| chr1:16130614 | G | A | 1 | a0002c0008t0003g0112 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2476-195C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 14/16 | chr1 | 16130614 | |||||||
| chr1:16130614 | G | C | 1 | a0001c0003t0001g0171 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2476-195C>G | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 14/16 | chr1 | 16130614 | |||||||
| chr1:16130631 | C | CT | 9 | a0001c0001t0001g0057 a0002c0008t0003g0014 a0002c0008t0003g0112 others(6): Show |
11 | HG00738.hp1 HG02572.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.2476-213dupA | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 14/16 | chr1 | 16130631 | |||||||
| chr1:16130705 | C | T | 2 | a0001c0005t0001g0130 a0001c0006t0001g0037 |
3 | HG01168.hp2 HG01169.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.2476-286G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 14/16 | chr1 | 16130705 | |||||||
| chr1:16130749 | C | T | 1 | a0001c0001t0001g0100 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2476-330G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 14/16 | chr1 | 16130749 | |||||||
| chr1:16130804 | A | T | 1 | a0001c0006t0001g0115 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.2476-385T>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 14/16 | chr1 | 16130804 | |||||||
| chr1:16130818 | T | C | 8 | a0002c0008t0003g0014 a0002c0008t0003g0112 a0002c0008t0003g0113 others(5): Show |
10 | HG02572.hp2 HG02717.hp1 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.2476-399A>G | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 14/16 | chr1 | 16130818 | |||||||
| chr1:16130997 | C | T | 1 | a0001c0002t0004g0094 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.2476-578G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 14/16 | chr1 | 16130997 | |||||||
| chr1:16131191 | T | C | 1 | a0001c0001t0002g0076 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.2475+530A>G | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 14/16 | chr1 | 16131191 | |||||||
| chr1:16131307 | C | T | 1 | a0001c0005t0007g0122 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2475+414G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 14/16 | chr1 | 16131307 | |||||||
| chr1:16131577 | T | C | 1 | a0001c0001t0001g0174 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2475+144A>G | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 14/16 | chr1 | 16131577 | |||||||
| chr1:16131581 | C | CA | 6 | a0001c0001t0001g0204 a0001c0001t0001g0207 a0001c0002t0001g0031 others(3): Show |
7 | HG01106.hp1 HG01167.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.2475+139dupT | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 14/16 | chr1 | 16131581 | |||||||
| chr1:16131594 | T | A | 5 | a0001c0001t0001g0204 a0001c0001t0001g0207 a0001c0002t0001g0031 others(2): Show |
6 | HG01106.hp1 HG01167.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.2475+127A>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 14/16 | chr1 | 16131594 | |||||||
| chr1:16131689 | C | T | 1 | a0001c0005t0007g0122 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2475+32G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 14/16 | chr1 | 16131689 | |||||||
| chr1:16131690 | G | C | 1 | a0001c0001t0001g0059 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.2475+31C>G | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 14/16 | chr1 | 16131690 | |||||||
| chr1:16131692 | A | G | 13 | a0001c0001t0001g0204 a0001c0001t0001g0207 a0001c0002t0001g0031 others(10): Show |
16 | HG01106.hp1 HG01167.hp1 HG02572.hp2 others(13): Show |
intron_variant | MODIFIER | c.2475+29T>C | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 14/16 | chr1 | 16131692 | |||||||
| chr1:16131919 | A | G | 1 | a0001c0006t0001g0115 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.2326-49T>C | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 13/16 | chr1 | 16131919 | |||||||
| chr1:16132016 | T | C | 1 | a0001c0001t0001g0150 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.2325+48A>G | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 13/16 | chr1 | 16132016 | |||||||
| chr1:16132319 | C | T | 41 | a0001c0003t0001g0007 a0001c0003t0001g0013 a0001c0003t0001g0041 others(38): Show |
50 | HG00099.hp1 HG00642.hp2 HG01109.hp1 others(47): Show |
intron_variant | MODIFIER | c.2116-46G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 12/16 | chr1 | 16132319 | |||||||
| chr1:16132353 | C | T | 8 | a0002c0008t0003g0014 a0002c0008t0003g0112 a0002c0008t0003g0113 others(5): Show |
10 | HG02572.hp2 HG02717.hp1 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.2115+25G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 12/16 | chr1 | 16132353 | |||||||
| chr1:16132546 | G | A | 1 | a0001c0001t0001g0060 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.2054-107C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 11/16 | chr1 | 16132546 | |||||||
| chr1:16132694 | CAGGTGGG others(79): Show |
C | 1 | a0001c0002t0001g0156 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2054-341_2054-256d others(88): Show |
EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 11/16 | chr1 | 16132694 | |||||||
| chr1:16132748 | GGGTGTAA others(122): Show |
G | 1 | a0001c0001t0001g0018 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.2053+303_2054-310d others(2): Show |
EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 11/16 | chr1 | 16132748 | |||||||
| chr1:16132834 | G | A | 1 | a0001c0002t0001g0031 | 2 | HG02886.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2053+346C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 11/16 | chr1 | 16132834 | |||||||
| chr1:16132856 | G | A | 1 | a0001c0001t0001g0212 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2053+324C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 11/16 | chr1 | 16132856 | |||||||
| chr1:16132859 | TG | T | 8 | a0002c0008t0003g0014 a0002c0008t0003g0112 a0002c0008t0003g0113 others(5): Show |
10 | HG02572.hp2 HG02717.hp1 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.2053+320delC | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 11/16 | chr1 | 16132859 | |||||||
| chr1:16132867 | A | C | 1 | a0001c0003t0001g0194 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.2053+313T>G | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 11/16 | chr1 | 16132867 | |||||||
| chr1:16132883 | AAGGAGGT others(122): Show |
A | 1 | a0001c0004t0001g0205 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2053+168_2053+296d others(2): Show |
EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 11/16 | chr1 | 16132883 | |||||||
| chr1:16132904 | G | A | 1 | a0007c0022t0001g0218 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.2053+276C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 11/16 | chr1 | 16132904 | |||||||
| chr1:16132929 | G | GGTGGGTA others(115): Show |
8 | a0002c0008t0003g0014 a0002c0008t0003g0112 a0002c0008t0003g0113 others(5): Show |
10 | HG02572.hp2 HG02717.hp1 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.2053+250_2053+251i others(124): Show |
EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 11/16 | chr1 | 16132929 | |||||||
| chr1:16133012 | T | A | 85 | a0001c0001t0001g0085 a0001c0001t0001g0100 a0001c0001t0001g0111 others(82): Show |
108 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(105): Show |
intron_variant | MODIFIER | c.2053+168A>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 11/16 | chr1 | 16133012 | |||||||
| chr1:16133101 | G | A | 1 | a0001c0004t0001g0140 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2053+79C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 11/16 | chr1 | 16133101 | |||||||
| chr1:16133129 | C | T | 1 | a0001c0001t0001g0085 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2053+51G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 11/16 | chr1 | 16133129 | |||||||
| chr1:16133142 | C | T | 11 | a0001c0004t0001g0009 a0001c0004t0001g0021 a0001c0004t0001g0024 others(8): Show |
19 | HG01884.hp2 HG01891.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.2053+38G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 11/16 | chr1 | 16133142 | |||||||
| chr1:16133469 | G | A | 3 | a0001c0002t0001g0050 a0001c0002t0001g0183 a0001c0002t0001g0210 |
3 | HG02886.hp2 HG02970.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1864+12C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 10/16 | chr1 | 16133469 | |||||||
| chr1:16133634 | G | A | 1 | a0004c0011t0001g0209 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1739-28C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 9/16 | chr1 | 16133634 | |||||||
| chr1:16133723 | C | T | 1 | a0001c0001t0001g0204 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1739-117G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 9/16 | chr1 | 16133723 | |||||||
| chr1:16133744 | C | T | 1 | a0001c0001t0001g0056 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1738+116G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 9/16 | chr1 | 16133744 | |||||||
| chr1:16133818 | G | T | 1 | a0007c0022t0001g0218 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1738+42C>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 9/16 | chr1 | 16133818 | |||||||
| chr1:16133844 | G | A | 69 | a0001c0001t0001g0085 a0001c0001t0001g0162 a0001c0001t0001g0178 others(66): Show |
89 | HG00099.hp1 HG00642.hp2 HG01069.hp1 others(86): Show |
intron_variant | MODIFIER | c.1738+16C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 9/16 | chr1 | 16133844 | |||||||
| chr1:16134046 | T | C | 84 | a0001c0001t0001g0085 a0001c0001t0001g0100 a0001c0001t0001g0111 others(81): Show |
106 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(103): Show |
intron_variant | MODIFIER | c.1683-131A>G | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 8/16 | chr1 | 16134046 | |||||||
| chr1:16134080 | C | T | 1 | a0001c0001t0001g0147 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1683-165G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 8/16 | chr1 | 16134080 | |||||||
| chr1:16134081 | G | A | 1 | a0001c0003t0001g0164 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1683-166C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 8/16 | chr1 | 16134081 | |||||||
| chr1:16134090 | G | A | 1 | a0001c0034t0001g0217 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1683-175C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 8/16 | chr1 | 16134090 | |||||||
| chr1:16134117 | G | A | 2 | a0004c0011t0001g0044 a0004c0011t0001g0209 |
3 | HG02257.hp1 HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1683-202C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 8/16 | chr1 | 16134117 | |||||||
| chr1:16134201 | G | A | 2 | a0001c0001t0001g0025 a0001c0001t0001g0075 |
3 | HG00642.hp1 HG01168.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.1682+267C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 8/16 | chr1 | 16134201 | |||||||
| chr1:16134248 | TAAC | T | 210 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(207): Show |
304 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(301): Show |
intron_variant | MODIFIER | c.1682+217_1682+219d others(5): Show |
EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 8/16 | chr1 | 16134248 | |||||||
| chr1:16134345 | G | A | 68 | a0001c0001t0001g0085 a0001c0001t0001g0162 a0001c0001t0001g0178 others(65): Show |
88 | HG00099.hp1 HG00642.hp2 HG01069.hp1 others(85): Show |
intron_variant | MODIFIER | c.1682+123C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 8/16 | chr1 | 16134345 | |||||||
| chr1:16134626 | G | A | 11 | a0001c0004t0001g0009 a0001c0004t0001g0021 a0001c0004t0001g0024 others(8): Show |
19 | HG01884.hp2 HG01891.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.1583-59C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 7/16 | chr1 | 16134626 | |||||||
| chr1:16134725 | G | T | 9 | a0001c0036t0001g0110 a0002c0008t0003g0014 a0002c0008t0003g0112 others(6): Show |
11 | HG02572.hp2 HG02717.hp1 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.1583-158C>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 7/16 | chr1 | 16134725 | |||||||
| chr1:16134799 | C | T | 1 | a0001c0003t0001g0194 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1583-232G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 7/16 | chr1 | 16134799 | |||||||
| chr1:16134841 | C | T | 2 | a0001c0006t0001g0036 a0001c0010t0001g0151 |
3 | HG00099.hp2 HG02300.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1582+195G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 7/16 | chr1 | 16134841 | |||||||
| chr1:16135338 | C | T | 65 | a0001c0001t0001g0085 a0001c0001t0001g0111 a0001c0001t0001g0162 others(62): Show |
83 | HG00099.hp1 HG00642.hp2 HG01069.hp1 others(80): Show |
intron_variant | MODIFIER | c.1429-149G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 6/16 | chr1 | 16135338 | |||||||
| chr1:16135505 | G | A | 5 | a0001c0001t0001g0100 a0001c0001t0001g0204 a0001c0001t0001g0207 others(2): Show |
5 | HG01106.hp1 HG01167.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1428+150C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 6/16 | chr1 | 16135505 | |||||||
| chr1:16135645 | T | G | 1 | a0001c0005t0001g0128 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1428+10A>C | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 6/16 | chr1 | 16135645 | |||||||
| chr1:16135790 | G | A | 1 | a0001c0001t0001g0085 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1313-20C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16135790 | |||||||
| chr1:16135902 | G | A | 1 | a0001c0003t0001g0194 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1313-132C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16135902 | |||||||
| chr1:16136150 | C | T | 1 | a0001c0002t0002g0092 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1313-380G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16136150 | |||||||
| chr1:16136303 | A | AAAT | 128 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(125): Show |
194 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.1313-536_1313-534d others(5): Show |
EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16136303 | |||||||
| chr1:16136303 | A | AAATAAT | 14 | a0001c0001t0001g0066 a0001c0001t0001g0069 a0001c0001t0001g0073 others(11): Show |
16 | HG00438.hp1 HG01074.hp2 HG01993.hp2 others(13): Show |
intron_variant | MODIFIER | c.1313-539_1313-534d others(8): Show |
EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16136303 | |||||||
| chr1:16136303 | A | AAATAATA others(2): Show |
13 | a0001c0002t0001g0080 a0001c0002t0001g0202 a0001c0004t0001g0208 others(10): Show |
24 | HG00639.hp2 HG00738.hp2 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.1313-542_1313-534d others(11): Show |
EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16136303 | |||||||
| chr1:16136303 | A | AAATAATA others(5): Show |
13 | a0001c0001t0001g0085 a0001c0001t0001g0162 a0001c0001t0001g0178 others(10): Show |
14 | HG01069.hp1 HG01071.hp2 HG01515.hp2 others(11): Show |
intron_variant | MODIFIER | c.1313-545_1313-534d others(14): Show |
EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16136303 | |||||||
| chr1:16136303 | A | AAATAATA others(8): Show |
5 | a0001c0001t0001g0204 a0001c0001t0001g0207 a0001c0002t0001g0084 others(2): Show |
7 | HG01106.hp1 HG01884.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.1313-548_1313-534d others(17): Show |
EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16136303 | |||||||
| chr1:16136303 | A | AAATAATA others(11): Show |
1 | a0001c0005t0001g0126 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1313-551_1313-534d others(20): Show |
EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16136303 | |||||||
| chr1:16136303 | AAATAATA others(5): Show |
A | 9 | a0001c0036t0001g0110 a0002c0008t0003g0014 a0002c0008t0003g0112 others(6): Show |
11 | HG02572.hp2 HG02717.hp1 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.1313-545_1313-534d others(14): Show |
EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16136303 | |||||||
| chr1:16136384 | C | T | 3 | a0001c0004t0001g0046 a0001c0004t0001g0047 a0001c0032t0001g0048 |
3 | HG00642.hp2 HG02976.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1313-614G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16136384 | |||||||
| chr1:16136583 | C | T | 1 | a0001c0034t0001g0217 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1313-813G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16136583 | |||||||
| chr1:16136626 | AAAG | A | 6 | a0001c0001t0001g0204 a0001c0001t0001g0207 a0001c0002t0001g0202 others(3): Show |
6 | HG01106.hp1 HG01167.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.1313-859_1313-857d others(5): Show |
EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16136626 | |||||||
| chr1:16136652 | AAAGAAGA others(34): Show |
A | 5 | a0001c0001t0001g0111 a0001c0003t0001g0165 a0001c0003t0001g0169 others(2): Show |
5 | HG00642.hp2 HG02451.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.1313-923_1313-883d others(43): Show |
EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16136652 | |||||||
| chr1:16136654 | AGAAGAAG others(31): Show |
A | 7 | a0001c0003t0001g0007 a0001c0003t0001g0167 a0001c0003t0001g0177 others(4): Show |
7 | HG01256.hp2 HG01934.hp1 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.1313-922_1313-885d others(40): Show |
EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16136654 | |||||||
| chr1:16136655 | GAAGAAGA others(19): Show |
G | 21 | a0001c0003t0001g0007 a0001c0003t0001g0041 a0001c0003t0001g0042 others(18): Show |
24 | HG00099.hp1 HG01884.hp2 HG02027.hp2 others(21): Show |
intron_variant | MODIFIER | c.1313-911_1313-886d others(28): Show |
EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16136655 | |||||||
| chr1:16136657 | AGAAGAAA others(28): Show |
A | 7 | a0001c0001t0001g0212 a0001c0003t0001g0172 a0001c0004t0001g0140 others(4): Show |
7 | HG02300.hp1 HG02572.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1313-922_1313-888d others(37): Show |
EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16136657 | |||||||
| chr1:16136660 | AGAAAAGA others(25): Show |
A | 8 | a0001c0003t0001g0007 a0001c0003t0001g0041 a0001c0003t0001g0042 others(5): Show |
10 | HG01891.hp2 HG02135.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.1313-922_1313-891d others(34): Show |
EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16136660 | |||||||
| chr1:16136661 | GAAAAGAA others(13): Show |
G | 4 | a0001c0003t0001g0170 a0001c0003t0001g0173 a0001c0004t0001g0024 others(1): Show |
5 | HG01109.hp1 HG02622.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.1313-911_1313-892d others(22): Show |
EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16136661 | |||||||
| chr1:16136663 | AAAGAAGA others(7): Show |
A | 1 | a0001c0003t0001g0171 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1313-907_1313-894d others(16): Show |
EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16136663 | |||||||
| chr1:16136664 | A | G | 8 | a0001c0003t0001g0007 a0001c0003t0001g0013 a0001c0003t0001g0158 others(5): Show |
10 | HG02738.hp1 HG02922.hp1 HG03017.hp2 others(7): Show |
intron_variant | MODIFIER | c.1313-894T>C | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16136664 | |||||||
| chr1:16136666 | GAAGAAAA others(10): Show |
G | 4 | a0001c0003t0001g0013 a0001c0003t0001g0158 a0001c0003t0001g0159 others(1): Show |
6 | HG02738.hp1 HG03017.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.1313-913_1313-897d others(19): Show |
EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16136666 | |||||||
| chr1:16136666 | GAAGAAAA others(39): Show |
G | 2 | a0001c0004t0002g0108 a0001c0010t0001g0163 |
2 | HG02922.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.1313-942_1313-897d others(48): Show |
EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16136666 | |||||||
| chr1:16136666 | GAAGAAAA others(42): Show |
G | 2 | a0001c0003t0001g0007 a0001c0004t0001g0106 |
2 | NA18951.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1313-945_1313-897d others(51): Show |
EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16136666 | |||||||
| chr1:16136678 | A | G | 1 | a0001c0003t0001g0171 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1313-908T>C | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16136678 | |||||||
| chr1:16136681 | A | G | 1 | a0001c0003t0001g0171 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1313-911T>C | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16136681 | |||||||
| chr1:16136686 | A | G | 4 | a0001c0003t0001g0170 a0001c0003t0001g0173 a0001c0004t0001g0024 others(1): Show |
5 | HG01109.hp1 HG02622.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.1313-916T>C | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16136686 | |||||||
| chr1:16136692 | G | A | 9 | a0001c0003t0001g0013 a0001c0003t0001g0158 a0001c0003t0001g0159 others(6): Show |
12 | HG01109.hp1 HG02258.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.1313-922C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16136692 | |||||||
| chr1:16136692 | GGAAGAAG others(16): Show |
G | 4 | a0001c0002t0001g0082 a0006c0013t0003g0081 a0006c0013t0003g0123 others(1): Show |
4 | HG03130.hp1 HG03130.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1313-945_1313-923d others(25): Show |
EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16136692 | |||||||
| chr1:16136692 | GGAAGAAG others(19): Show |
G | 7 | a0001c0001t0001g0207 a0001c0002t0001g0084 a0001c0002t0001g0210 others(4): Show |
7 | HG02486.hp1 HG02717.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1313-948_1313-923d others(28): Show |
EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16136692 | |||||||
| chr1:16136692 | GGAAGAAG others(22): Show |
G | 5 | a0001c0001t0001g0204 a0001c0002t0001g0028 a0001c0002t0001g0080 others(2): Show |
6 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(3): Show |
intron_variant | MODIFIER | c.1313-951_1313-923d others(31): Show |
EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16136692 | |||||||
| chr1:16136692 | GGAAGAAG others(25): Show |
G | 1 | a0002c0008t0003g0014 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1313-954_1313-923d others(34): Show |
EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16136692 | |||||||
| chr1:16136692 | GGAAGAAG others(28): Show |
G | 1 | a0002c0035t0003g0200 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1313-957_1313-923d others(37): Show |
EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16136692 | |||||||
| chr1:16136692 | GGAAGAAG others(31): Show |
G | 1 | a0001c0001t0001g0162 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1313-960_1313-923d others(40): Show |
EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16136692 | |||||||
| chr1:16136692 | GGAAGAAG others(34): Show |
G | 1 | a0001c0001t0001g0178 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1313-963_1313-923d others(43): Show |
EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16136692 | |||||||
| chr1:16136693 | GAAGAAGA others(13): Show |
G | 4 | a0001c0001t0001g0085 a0001c0002t0001g0050 a0001c0002t0001g0183 others(1): Show |
4 | HG02572.hp2 HG02970.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1313-943_1313-924d others(22): Show |
EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16136693 | |||||||
| chr1:16136696 | GAAGAAGA others(10): Show |
G | 1 | a0001c0034t0001g0217 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1313-943_1313-927d others(19): Show |
EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16136696 | |||||||
| chr1:16136698 | A | G | 8 | a0001c0003t0001g0007 a0001c0003t0001g0041 a0001c0003t0001g0042 others(5): Show |
10 | HG01891.hp2 HG02135.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.1313-928T>C | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16136698 | |||||||
| chr1:16136699 | GAAGAAGA others(7): Show |
G | 3 | a0001c0001t0001g0100 a0001c0002t0001g0202 a0001c0036t0001g0110 |
3 | HG01167.hp1 HG02922.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1313-943_1313-930d others(16): Show |
EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16136699 | |||||||
| chr1:16136701 | A | G | 7 | a0001c0001t0001g0212 a0001c0003t0001g0172 a0001c0004t0001g0140 others(4): Show |
7 | HG02300.hp1 HG02572.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1313-931T>C | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16136701 | |||||||
| chr1:16136704 | A | G | 8 | a0001c0003t0001g0007 a0001c0003t0001g0167 a0001c0003t0001g0177 others(5): Show |
8 | HG00735.hp2 HG01256.hp2 HG01934.hp1 others(5): Show |
intron_variant | MODIFIER | c.1313-934T>C | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16136704 | |||||||
| chr1:16136707 | A | G | 5 | a0001c0001t0001g0111 a0001c0003t0001g0165 a0001c0003t0001g0169 others(2): Show |
5 | HG00642.hp2 HG02451.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.1313-937T>C | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16136707 | |||||||
| chr1:16136708 | GAAGAA | G | 12 | a0001c0003t0001g0007 a0001c0003t0001g0041 a0001c0003t0001g0042 others(9): Show |
13 | HG00099.hp1 HG02027.hp2 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.1313-943_1313-939d others(7): Show |
EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16136708 | |||||||
| chr1:16136711 | GAA | G | 41 | a0001c0001t0001g0111 a0001c0001t0001g0212 a0001c0003t0001g0007 others(38): Show |
50 | HG00642.hp2 HG01109.hp1 HG01256.hp2 others(47): Show |
intron_variant | MODIFIER | c.1313-943_1313-942d others(4): Show |
EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16136711 | |||||||
| chr1:16136713 | A | AAAG | 24 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0010 others(21): Show |
27 | HG00323.hp1 HG00609.hp2 HG00621.hp1 others(24): Show |
intron_variant | MODIFIER | c.1313-946_1313-944d others(5): Show |
EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16136713 | |||||||
| chr1:16136713 | A | AAAGAAG | 17 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0012 others(14): Show |
24 | HG00738.hp1 HG01167.hp2 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.1313-949_1313-944d others(8): Show |
EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16136713 | |||||||
| chr1:16136713 | A | AAAGAAGA others(2): Show |
25 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0020 others(22): Show |
32 | HG00323.hp2 HG00597.hp1 HG00673.hp2 others(29): Show |
intron_variant | MODIFIER | c.1313-952_1313-944d others(11): Show |
EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16136713 | |||||||
| chr1:16136713 | A | AAAGAAGA others(5): Show |
17 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0018 others(14): Show |
19 | HG00438.hp1 HG00558.hp1 HG00597.hp2 others(16): Show |
intron_variant | MODIFIER | c.1313-955_1313-944d others(14): Show |
EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16136713 | |||||||
| chr1:16136713 | A | AAAGAAGA others(8): Show |
12 | a0001c0001t0001g0001 a0001c0001t0001g0060 a0001c0001t0001g0102 others(9): Show |
14 | HG01109.hp2 HG01123.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.1313-958_1313-944d others(17): Show |
EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16136713 | |||||||
| chr1:16136713 | A | AAAGAAGA others(11): Show |
5 | a0001c0001t0001g0003 a0001c0001t0001g0053 a0001c0001t0001g0216 others(2): Show |
6 | HG00280.hp2 HG01261.hp1 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.1313-961_1313-944d others(20): Show |
EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16136713 | |||||||
| chr1:16136713 | A | AAAGAAGA others(14): Show |
4 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0005t0001g0002 others(1): Show |
6 | HG00639.hp1 HG01516.hp1 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.1313-964_1313-944d others(23): Show |
EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16136713 | |||||||
| chr1:16136713 | A | AAAGAAGA others(23): Show |
1 | a0009c0029t0001g0114 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1313-973_1313-944d others(32): Show |
EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16136713 | |||||||
| chr1:16136713 | A | AG | 6 | a0001c0001t0001g0051 a0001c0001t0002g0058 a0001c0003t0001g0157 others(3): Show |
6 | HG01884.hp2 HG02056.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.1313-944_1313-943i others(3): Show |
EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16136713 | |||||||
| chr1:16136713 | A | AGAAGAAG others(3): Show |
2 | a0001c0001t0002g0022 a0001c0005t0007g0122 |
2 | HG02559.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.1313-944_1313-943i others(12): Show |
EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16136713 | |||||||
| chr1:16136713 | A | AGAAGAAG others(6): Show |
2 | a0001c0001t0001g0003 a0001c0001t0001g0018 |
2 | HG00280.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.1313-944_1313-943i others(15): Show |
EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16136713 | |||||||
| chr1:16136713 | A | AGAAGAAG others(9): Show |
3 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0062 |
3 | HG00558.hp2 NA18954.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.1313-944_1313-943i others(18): Show |
EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16136713 | |||||||
| chr1:16136713 | A | AGAAGAAG others(18): Show |
1 | a0001c0001t0001g0075 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1313-944_1313-943i others(27): Show |
EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16136713 | |||||||
| chr1:16136713 | A | G | 2 | a0001c0004t0002g0108 a0001c0010t0001g0163 |
2 | HG02922.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.1313-943T>C | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16136713 | |||||||
| chr1:16136713 | AAAG | A | 25 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(22): Show |
27 | HG00609.hp1 HG00733.hp1 HG00733.hp2 others(24): Show |
intron_variant | MODIFIER | c.1313-946_1313-944d others(5): Show |
EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16136713 | |||||||
| chr1:16136713 | AAAGAAG | A | 8 | a0001c0001t0001g0019 a0001c0001t0002g0022 a0001c0001t0002g0101 others(5): Show |
10 | HG00099.hp2 HG01069.hp2 HG02300.hp2 others(7): Show |
intron_variant | MODIFIER | c.1313-949_1313-944d others(8): Show |
EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16136713 | |||||||
| chr1:16136713 | AAAGAAGA others(5): Show |
A | 1 | a0001c0006t0001g0004 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1313-955_1313-944d others(14): Show |
EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16136713 | |||||||
| chr1:16136713 | AAAGAAGA others(8): Show |
A | 1 | a0001c0001t0001g0010 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1313-958_1313-944d others(17): Show |
EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16136713 | |||||||
| chr1:16136757 | A | G | 1 | a0001c0004t0001g0184 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1313-987T>C | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16136757 | |||||||
| chr1:16136763 | A | G | 1 | a0001c0001t0001g0100 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1313-993T>C | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16136763 | |||||||
| chr1:16136773 | G | C | 4 | a0001c0001t0001g0204 a0001c0001t0001g0207 a0001c0002t0001g0202 others(1): Show |
4 | HG01106.hp1 HG01167.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.1313-1003C>G | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16136773 | |||||||
| chr1:16136773 | G | GAAGAAGA others(5): Show |
1 | a0001c0002t0001g0148 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1313-1004_1313-100 others(16): Show |
EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16136773 | |||||||
| chr1:16136797 | CT | C | 21 | a0001c0001t0001g0085 a0001c0001t0001g0162 a0001c0001t0001g0178 others(18): Show |
24 | HG01069.hp1 HG01071.hp2 HG02486.hp1 others(21): Show |
intron_variant | MODIFIER | c.1313-1028delA | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16136797 | |||||||
| chr1:16136861 | C | T | 1 | a0001c0001t0001g0100 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1312+992G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16136861 | |||||||
| chr1:16136934 | G | A | 1 | a0001c0006t0001g0134 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1312+919C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16136934 | |||||||
| chr1:16136978 | T | G | 1 | a0005c0017t0001g0175 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1312+875A>C | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16136978 | |||||||
| chr1:16137148 | A | T | 52 | a0001c0001t0001g0111 a0001c0001t0001g0212 a0001c0003t0001g0007 others(49): Show |
69 | HG00099.hp1 HG00642.hp2 HG01109.hp1 others(66): Show |
intron_variant | MODIFIER | c.1312+705T>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16137148 | |||||||
| chr1:16137191 | G | A | 1 | a0001c0001t0001g0068 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1312+662C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16137191 | |||||||
| chr1:16137297 | T | TAA | 26 | a0001c0001t0001g0085 a0001c0001t0001g0162 a0001c0001t0001g0178 others(23): Show |
29 | HG00735.hp2 HG01069.hp1 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.1312+554_1312+555d others(4): Show |
EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16137297 | |||||||
| chr1:16137297 | T | TAAA | 47 | a0001c0001t0001g0111 a0001c0001t0001g0212 a0001c0003t0001g0007 others(44): Show |
64 | HG00099.hp1 HG01109.hp1 HG01256.hp2 others(61): Show |
intron_variant | MODIFIER | c.1312+553_1312+555d others(5): Show |
EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16137297 | |||||||
| chr1:16137337 | G | T | 9 | a0001c0001t0001g0212 a0001c0003t0001g0164 a0001c0003t0001g0173 others(6): Show |
10 | HG00642.hp2 HG01109.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1312+516C>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16137337 | |||||||
| chr1:16137394 | C | T | 1 | a0001c0001t0001g0142 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1312+459G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16137394 | |||||||
| chr1:16137553 | A | G | 22 | a0001c0004t0001g0009 a0001c0004t0001g0024 a0001c0004t0001g0205 others(19): Show |
31 | HG01243.hp2 HG01884.hp2 HG01891.hp2 others(28): Show |
intron_variant | MODIFIER | c.1312+300T>C | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16137553 | |||||||
| chr1:16137645 | A | G | 4 | a0001c0001t0001g0204 a0001c0001t0001g0207 a0001c0002t0001g0202 others(1): Show |
4 | HG01106.hp1 HG01167.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.1312+208T>C | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16137645 | |||||||
| chr1:16137765 | T | C | 46 | a0001c0001t0001g0100 a0001c0001t0001g0111 a0001c0001t0001g0212 others(43): Show |
56 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(53): Show |
intron_variant | MODIFIER | c.1312+88A>G | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 5/16 | chr1 | 16137765 | |||||||
| chr1:16138441 | C | T | 5 | a0001c0001t0001g0162 a0001c0001t0001g0178 a0001c0003t0001g0164 others(2): Show |
5 | HG01109.hp1 HG02683.hp1 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.824-11G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16138441 | |||||||
| chr1:16138802 | C | T | 13 | a0001c0001t0001g0100 a0001c0001t0001g0204 a0001c0001t0001g0207 others(10): Show |
13 | HG01106.hp1 HG01167.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.824-372G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16138802 | |||||||
| chr1:16138908 | A | G | 53 | a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0056 others(50): Show |
70 | HG00099.hp1 HG00438.hp2 HG00597.hp1 others(67): Show |
intron_variant | MODIFIER | c.824-478T>C | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16138908 | |||||||
| chr1:16138909 | C | T | 53 | a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0056 others(50): Show |
70 | HG00099.hp1 HG00438.hp2 HG00597.hp1 others(67): Show |
intron_variant | MODIFIER | c.824-479G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16138909 | |||||||
| chr1:16139001 | C | T | 10 | a0001c0001t0001g0085 a0001c0002t0001g0028 a0001c0002t0001g0050 others(7): Show |
11 | HG01069.hp1 HG01071.hp2 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.824-571G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16139001 | |||||||
| chr1:16139306 | C | T | 1 | a0001c0001t0001g0204 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.824-876G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16139306 | |||||||
| chr1:16139508 | T | C | 47 | a0001c0001t0001g0111 a0001c0001t0001g0162 a0001c0001t0001g0178 others(44): Show |
63 | HG00099.hp1 HG00642.hp2 HG01109.hp1 others(60): Show |
intron_variant | MODIFIER | c.824-1078A>G | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16139508 | |||||||
| chr1:16139699 | G | A | 2 | a0004c0011t0001g0044 a0004c0011t0001g0209 |
3 | HG02257.hp1 HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.824-1269C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16139699 | |||||||
| chr1:16139752 | G | A | 3 | a0001c0001t0002g0022 a0001c0001t0002g0076 a0001c0001t0002g0190 |
5 | NA18961.hp1 NA18985.hp1 NA19000.hp1 others(2): Show |
intron_variant | MODIFIER | c.824-1322C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16139752 | |||||||
| chr1:16139795 | G | A | 1 | a0001c0024t0003g0086 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.824-1365C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16139795 | |||||||
| chr1:16139947 | C | T | 1 | a0001c0001t0001g0055 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.824-1517G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16139947 | |||||||
| chr1:16140039 | G | A | 5 | a0001c0001t0001g0212 a0001c0003t0001g0041 a0001c0003t0001g0157 others(2): Show |
6 | HG02027.hp2 HG02572.hp1 NA18973.hp1 others(3): Show |
intron_variant | MODIFIER | c.824-1609C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16140039 | |||||||
| chr1:16140085 | G | A | 1 | a0001c0003t0001g0172 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.824-1655C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16140085 | |||||||
| chr1:16140087 | G | C | 1 | a0001c0001t0001g0077 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.824-1657C>G | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16140087 | |||||||
| chr1:16140176 | G | A | 1 | a0007c0022t0001g0218 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.824-1746C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16140176 | |||||||
| chr1:16140204 | C | A | 1 | a0001c0001t0001g0051 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.824-1774G>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16140204 | |||||||
| chr1:16140232 | G | A | 1 | a0001c0033t0001g0099 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.824-1802C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16140232 | |||||||
| chr1:16140397 | C | T | 1 | a0001c0002t0001g0202 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.824-1967G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16140397 | |||||||
| chr1:16140767 | G | A | 1 | a0001c0003t0001g0160 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.824-2337C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16140767 | |||||||
| chr1:16140771 | A | G | 4 | a0001c0001t0001g0204 a0001c0001t0001g0207 a0001c0004t0001g0205 others(1): Show |
4 | HG01106.hp1 HG02723.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.824-2341T>C | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16140771 | |||||||
| chr1:16140853 | G | A | 23 | a0001c0001t0001g0085 a0001c0001t0001g0100 a0001c0001t0001g0204 others(20): Show |
24 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.824-2423C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16140853 | |||||||
| chr1:16140890 | C | T | 1 | a0001c0009t0001g0196 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.824-2460G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16140890 | |||||||
| chr1:16140896 | C | T | 139 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(136): Show |
199 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.824-2466G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16140896 | |||||||
| chr1:16141150 | T | G | 118 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(115): Show |
179 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(176): Show |
intron_variant | MODIFIER | c.824-2720A>C | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16141150 | |||||||
| chr1:16141429 | G | T | 119 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(116): Show |
180 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(177): Show |
intron_variant | MODIFIER | c.824-2999C>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16141429 | |||||||
| chr1:16141478 | G | A | 22 | a0001c0001t0001g0085 a0001c0001t0001g0100 a0001c0001t0001g0204 others(19): Show |
23 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.824-3048C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16141478 | |||||||
| chr1:16141680 | C | T | 6 | a0001c0001t0001g0111 a0001c0004t0002g0032 a0001c0004t0002g0107 others(3): Show |
9 | HG02451.hp1 HG02572.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.824-3250G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16141680 | |||||||
| chr1:16141710 | C | T | 1 | a0001c0004t0001g0161 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.824-3280G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16141710 | |||||||
| chr1:16141730 | A | G | 1 | a0001c0001t0001g0100 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.824-3300T>C | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16141730 | |||||||
| chr1:16142040 | C | T | 1 | a0001c0027t0001g0199 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.824-3610G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16142040 | |||||||
| chr1:16142372 | T | A | 22 | a0001c0001t0001g0085 a0001c0001t0001g0100 a0001c0001t0001g0204 others(19): Show |
23 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.824-3942A>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16142372 | |||||||
| chr1:16142463 | A | G | 2 | a0001c0001t0002g0101 a0001c0001t0002g0181 |
2 | NA18975.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.824-4033T>C | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16142463 | |||||||
| chr1:16142627 | ATGGATGG others(129): Show |
A | 1 | a0001c0001t0001g0062 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.824-4333_824-4198d others(2): Show |
EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16142627 | |||||||
| chr1:16142684 | G | A | 14 | a0001c0001t0001g0100 a0001c0001t0001g0204 a0001c0001t0001g0207 others(11): Show |
14 | HG01106.hp1 HG01167.hp1 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.824-4254C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16142684 | |||||||
| chr1:16142789 | A | G | 22 | a0001c0001t0001g0085 a0001c0001t0001g0100 a0001c0001t0001g0204 others(19): Show |
23 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.824-4359T>C | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16142789 | |||||||
| chr1:16142814 | CGGGATGG others(124): Show |
C | 1 | a0001c0015t0001g0182 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.824-4515_824-4385d others(2): Show |
EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16142814 | |||||||
| chr1:16142869 | G | A | 4 | a0001c0001t0001g0204 a0001c0001t0001g0207 a0001c0004t0001g0205 others(1): Show |
4 | HG01106.hp1 HG02723.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.824-4439C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16142869 | |||||||
| chr1:16142984 | A | AATGG | 11 | a0001c0001t0001g0100 a0001c0001t0001g0207 a0001c0002t0001g0202 others(8): Show |
11 | HG00673.hp1 HG01167.hp1 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.824-4558_824-4555d others(6): Show |
EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16142984 | |||||||
| chr1:16142984 | A | AATGGATG others(1): Show |
99 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(96): Show |
151 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.824-4562_824-4555d others(10): Show |
EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16142984 | |||||||
| chr1:16142984 | A | AATGGATG others(5): Show |
18 | a0001c0001t0001g0038 a0001c0001t0001g0054 a0001c0002t0001g0039 others(15): Show |
20 | HG00323.hp2 HG00642.hp2 HG00735.hp1 others(17): Show |
intron_variant | MODIFIER | c.824-4566_824-4555d others(14): Show |
EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16142984 | |||||||
| chr1:16142984 | A | AATGGATG others(9): Show |
1 | a0001c0036t0001g0110 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.824-4570_824-4555d others(18): Show |
EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16142984 | |||||||
| chr1:16143134 | C | T | 1 | a0001c0034t0001g0217 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.824-4704G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16143134 | |||||||
| chr1:16143158 | T | TGATG | 74 | a0001c0001t0001g0019 a0001c0001t0001g0102 a0001c0001t0001g0141 others(71): Show |
106 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.824-4732_824-4729d others(6): Show |
EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16143158 | |||||||
| chr1:16143158 | T | TGATGGAT others(1): Show |
106 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(103): Show |
165 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.824-4736_824-4729d others(10): Show |
EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16143158 | |||||||
| chr1:16143158 | T | TGATGGAT others(5): Show |
21 | a0001c0001t0001g0079 a0001c0001t0001g0085 a0001c0001t0001g0100 others(18): Show |
22 | HG01106.hp1 HG01106.hp2 HG01167.hp1 others(19): Show |
intron_variant | MODIFIER | c.824-4740_824-4729d others(14): Show |
EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16143158 | |||||||
| chr1:16143158 | T | TGATGGAT others(9): Show |
6 | a0001c0002t0001g0028 a0001c0002t0001g0050 a0001c0002t0001g0082 others(3): Show |
7 | HG01069.hp1 HG01071.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.824-4744_824-4729d others(18): Show |
EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16143158 | |||||||
| chr1:16143191 | A | G | 3 | a0001c0001t0001g0018 a0001c0001t0001g0146 a0001c0001t0001g0188 |
5 | HG00280.hp1 HG01257.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.824-4761T>C | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16143191 | |||||||
| chr1:16143251 | G | C | 1 | a0002c0035t0003g0200 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.824-4821C>G | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16143251 | |||||||
| chr1:16143322 | T | C | 1 | a0001c0003t0001g0173 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.824-4892A>G | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16143322 | |||||||
| chr1:16143430 | C | T | 20 | a0001c0001t0001g0085 a0001c0001t0001g0100 a0001c0001t0001g0204 others(17): Show |
21 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(18): Show |
intron_variant | MODIFIER | c.823+4948G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16143430 | |||||||
| chr1:16143436 | T | C | 1 | a0001c0001t0001g0100 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.823+4942A>G | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16143436 | |||||||
| chr1:16143442 | AC | A | 8 | a0001c0001t0001g0204 a0001c0001t0001g0207 a0001c0002t0001g0202 others(5): Show |
8 | HG01106.hp1 HG01167.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.823+4935delG | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16143442 | |||||||
| chr1:16143533 | A | G | 2 | a0001c0006t0001g0087 a0001c0006t0001g0121 |
2 | HG03017.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.823+4845T>C | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16143533 | |||||||
| chr1:16143921 | G | A | 8 | a0001c0001t0001g0204 a0001c0001t0001g0207 a0001c0002t0001g0202 others(5): Show |
8 | HG01106.hp1 HG01167.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.823+4457C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16143921 | |||||||
| chr1:16143937 | C | G | 1 | a0001c0003t0001g0157 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.823+4441G>C | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16143937 | |||||||
| chr1:16144047 | C | T | 1 | a0001c0004t0001g0184 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.823+4331G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16144047 | |||||||
| chr1:16144191 | C | T | 8 | a0001c0001t0001g0085 a0001c0002t0001g0028 a0001c0002t0001g0050 others(5): Show |
9 | HG01069.hp1 HG01071.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.823+4187G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16144191 | |||||||
| chr1:16144295 | G | A | 1 | a0001c0001t0001g0078 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.823+4083C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16144295 | |||||||
| chr1:16144383 | G | A | 2 | a0001c0001t0001g0006 a0001c0001t0001g0191 |
5 | HG02129.hp2 NA18944.hp2 NA18957.hp1 others(2): Show |
intron_variant | MODIFIER | c.823+3995C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16144383 | |||||||
| chr1:16144447 | C | A | 1 | a0001c0001t0001g0085 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.823+3931G>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16144447 | |||||||
| chr1:16144505 | G | T | 54 | a0001c0001t0001g0100 a0001c0002t0001g0156 a0001c0005t0001g0002 others(51): Show |
81 | HG00099.hp2 HG00323.hp1 HG00639.hp2 others(78): Show |
intron_variant | MODIFIER | c.823+3873C>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16144505 | |||||||
| chr1:16144648 | C | T | 1 | a0001c0016t0001g0033 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.823+3730G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16144648 | |||||||
| chr1:16144673 | T | G | 1 | a0001c0001t0001g0153 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.823+3705A>C | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16144673 | |||||||
| chr1:16144791 | T | A | 1 | a0001c0027t0001g0199 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.823+3587A>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16144791 | |||||||
| chr1:16144798 | CCCCCGTT | C | 18 | a0001c0001t0001g0085 a0001c0001t0001g0204 a0001c0001t0001g0207 others(15): Show |
19 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(16): Show |
intron_variant | MODIFIER | c.823+3573_823+3579d others(9): Show |
EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16144798 | |||||||
| chr1:16144960 | A | G | 56 | a0001c0001t0001g0100 a0001c0002t0001g0050 a0001c0002t0001g0082 others(53): Show |
83 | HG00099.hp2 HG00323.hp1 HG00639.hp2 others(80): Show |
intron_variant | MODIFIER | c.823+3418T>C | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16144960 | |||||||
| chr1:16145202 | G | A | 2 | a0002c0008t0003g0112 a0002c0008t0003g0113 |
2 | HG02717.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.823+3176C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16145202 | |||||||
| chr1:16145202 | G | C | 5 | a0001c0001t0001g0011 a0001c0001t0001g0053 a0001c0001t0001g0216 others(2): Show |
7 | HG00280.hp2 HG00558.hp1 HG00673.hp2 others(4): Show |
intron_variant | MODIFIER | c.823+3176C>G | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16145202 | |||||||
| chr1:16145247 | G | T | 1 | a0013c0025t0001g0120 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.823+3131C>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16145247 | |||||||
| chr1:16145289 | G | A | 1 | a0001c0001t0001g0192 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.823+3089C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16145289 | |||||||
| chr1:16145333 | G | A | 2 | a0001c0001t0001g0085 a0001c0004t0001g0154 |
2 | HG03139.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.823+3045C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16145333 | |||||||
| chr1:16145341 | C | T | 1 | a0001c0001t0001g0053 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.823+3037G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16145341 | |||||||
| chr1:16145454 | C | G | 1 | a0002c0008t0003g0112 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.823+2924G>C | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16145454 | |||||||
| chr1:16145511 | C | T | 8 | a0001c0001t0001g0085 a0001c0002t0001g0028 a0001c0002t0001g0050 others(5): Show |
9 | HG01069.hp1 HG01071.hp2 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.823+2867G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16145511 | |||||||
| chr1:16145535 | G | T | 1 | a0001c0001t0001g0204 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.823+2843C>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16145535 | |||||||
| chr1:16145791 | C | T | 1 | a0003c0007t0001g0119 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.823+2587G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16145791 | |||||||
| chr1:16145840 | T | G | 1 | a0001c0001t0001g0141 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.823+2538A>C | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16145840 | |||||||
| chr1:16145881 | T | C | 1 | a0009c0029t0001g0114 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.823+2497A>G | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16145881 | |||||||
| chr1:16145940 | C | G | 1 | a0001c0003t0001g0155 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.823+2438G>C | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16145940 | |||||||
| chr1:16146015 | A | G | 16 | a0001c0001t0001g0085 a0001c0001t0001g0204 a0001c0001t0001g0207 others(13): Show |
17 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.823+2363T>C | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16146015 | |||||||
| chr1:16146037 | G | A | 1 | a0006c0013t0003g0081 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.823+2341C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16146037 | |||||||
| chr1:16146111 | C | T | 16 | a0001c0001t0001g0085 a0001c0001t0001g0204 a0001c0001t0001g0207 others(13): Show |
17 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.823+2267G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16146111 | |||||||
| chr1:16146125 | C | A | 16 | a0001c0001t0001g0085 a0001c0001t0001g0204 a0001c0001t0001g0207 others(13): Show |
17 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.823+2253G>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16146125 | |||||||
| chr1:16146184 | C | T | 2 | a0002c0008t0003g0112 a0002c0008t0003g0113 |
2 | HG02717.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.823+2194G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16146184 | |||||||
| chr1:16146223 | C | T | 3 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0003t0001g0145 |
3 | HG01074.hp2 HG03710.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.823+2155G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16146223 | |||||||
| chr1:16146234 | G | C | 16 | a0001c0001t0001g0085 a0001c0001t0001g0204 a0001c0001t0001g0207 others(13): Show |
17 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.823+2144C>G | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16146234 | |||||||
| chr1:16146293 | G | T | 1 | a0001c0001t0002g0052 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.823+2085C>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16146293 | |||||||
| chr1:16146329 | G | T | 2 | a0002c0008t0003g0112 a0002c0008t0003g0113 |
2 | HG02717.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.823+2049C>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16146329 | |||||||
| chr1:16146339 | C | A | 31 | a0001c0001t0001g0162 a0001c0001t0001g0178 a0001c0001t0001g0212 others(28): Show |
36 | HG00099.hp1 HG00642.hp2 HG01109.hp1 others(33): Show |
intron_variant | MODIFIER | c.823+2039G>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16146339 | |||||||
| chr1:16146391 | C | T | 1 | a0002c0035t0003g0200 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.823+1987G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16146391 | |||||||
| chr1:16146408 | C | T | 1 | a0001c0004t0002g0107 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.823+1970G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16146408 | |||||||
| chr1:16146432 | G | A | 1 | a0001c0001t0001g0174 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.823+1946C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16146432 | |||||||
| chr1:16146464 | C | G | 1 | a0001c0001t0001g0142 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.823+1914G>C | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16146464 | |||||||
| chr1:16146498 | C | T | 53 | a0001c0005t0001g0002 a0001c0005t0001g0015 a0001c0005t0001g0016 others(50): Show |
80 | HG00099.hp2 HG00323.hp1 HG00639.hp2 others(77): Show |
intron_variant | MODIFIER | c.823+1880G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16146498 | |||||||
| chr1:16146591 | G | A | 1 | a0001c0006t0001g0118 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.823+1787C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16146591 | |||||||
| chr1:16146592 | G | A | 1 | a0001c0034t0001g0217 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.823+1786C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16146592 | |||||||
| chr1:16146595 | C | T | 1 | a0001c0001t0001g0111 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.823+1783G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16146595 | |||||||
| chr1:16146599 | T | G | 1 | a0005c0017t0001g0175 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.823+1779A>C | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16146599 | |||||||
| chr1:16146621 | C | G | 1 | a0001c0002t0004g0094 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.823+1757G>C | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16146621 | |||||||
| chr1:16146642 | A | G | 1 | a0001c0034t0001g0217 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.823+1736T>C | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16146642 | |||||||
| chr1:16146718 | C | T | 2 | a0001c0006t0001g0118 a0011c0028t0001g0117 |
2 | HG02698.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.823+1660G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16146718 | |||||||
| chr1:16146801 | G | T | 1 | a0002c0035t0003g0200 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.823+1577C>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16146801 | |||||||
| chr1:16146888 | T | C | 1 | a0001c0001t0001g0100 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.823+1490A>G | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16146888 | |||||||
| chr1:16147019 | A | G | 65 | a0001c0001t0001g0204 a0001c0001t0001g0207 a0001c0002t0001g0202 others(62): Show |
92 | HG00099.hp2 HG00323.hp1 HG00639.hp2 others(89): Show |
intron_variant | MODIFIER | c.823+1359T>C | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16147019 | |||||||
| chr1:16147096 | A | G | 1 | a0001c0004t0001g0106 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.823+1282T>C | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16147096 | |||||||
| chr1:16147163 | C | T | 1 | a0001c0024t0003g0086 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.823+1215G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16147163 | |||||||
| chr1:16147266 | G | T | 1 | a0001c0004t0001g0106 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.823+1112C>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16147266 | |||||||
| chr1:16147275 | T | C | 11 | a0001c0001t0001g0204 a0001c0001t0001g0207 a0001c0002t0001g0202 others(8): Show |
11 | HG01106.hp1 HG01167.hp1 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.823+1103A>G | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16147275 | |||||||
| chr1:16147450 | G | A | 7 | a0001c0001t0001g0085 a0001c0002t0001g0028 a0001c0002t0001g0050 others(4): Show |
8 | HG01069.hp1 HG01071.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.823+928C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16147450 | |||||||
| chr1:16147484 | T | C | 197 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(194): Show |
285 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(282): Show |
intron_variant | MODIFIER | c.823+894A>G | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16147484 | |||||||
| chr1:16147546 | G | A | 8 | a0001c0001t0001g0204 a0001c0001t0001g0207 a0001c0002t0001g0202 others(5): Show |
8 | HG01106.hp1 HG01167.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.823+832C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16147546 | |||||||
| chr1:16147561 | C | T | 1 | a0001c0001t0001g0051 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.823+817G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16147561 | |||||||
| chr1:16147615 | C | G | 103 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(100): Show |
158 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(155): Show |
intron_variant | MODIFIER | c.823+763G>C | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16147615 | |||||||
| chr1:16147631 | C | T | 9 | a0001c0001t0001g0204 a0001c0001t0001g0207 a0001c0002t0001g0202 others(6): Show |
9 | HG01106.hp1 HG01167.hp1 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.823+747G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16147631 | |||||||
| chr1:16147633 | T | C | 2 | a0002c0008t0003g0112 a0002c0008t0003g0113 |
2 | HG02717.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.823+745A>G | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16147633 | |||||||
| chr1:16147772 | C | T | 1 | a0001c0004t0001g0106 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.823+606G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16147772 | |||||||
| chr1:16147865 | T | G | 9 | a0001c0001t0001g0204 a0001c0001t0001g0207 a0001c0002t0001g0202 others(6): Show |
9 | HG01106.hp1 HG01167.hp1 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.823+513A>C | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16147865 | |||||||
| chr1:16147922 | A | G | 9 | a0001c0001t0001g0204 a0001c0001t0001g0207 a0001c0002t0001g0202 others(6): Show |
9 | HG01106.hp1 HG01167.hp1 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.823+456T>C | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16147922 | |||||||
| chr1:16148059 | A | G | 1 | a0001c0001t0001g0067 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.823+319T>C | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16148059 | |||||||
| chr1:16148068 | G | A | 1 | a0001c0034t0001g0217 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.823+310C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16148068 | |||||||
| chr1:16148169 | C | A | 1 | a0001c0001t0001g0066 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.823+209G>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16148169 | |||||||
| chr1:16148206 | G | A | 88 | a0001c0001t0001g0085 a0001c0001t0001g0102 a0001c0001t0001g0204 others(85): Show |
118 | HG00099.hp2 HG00323.hp1 HG00639.hp2 others(115): Show |
intron_variant | MODIFIER | c.823+172C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16148206 | |||||||
| chr1:16148344 | AC | A | 88 | a0001c0001t0001g0085 a0001c0001t0001g0102 a0001c0001t0001g0204 others(85): Show |
118 | HG00099.hp2 HG00323.hp1 HG00639.hp2 others(115): Show |
intron_variant | MODIFIER | c.823+33delG | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 3/16 | chr1 | 16148344 | |||||||
| chr1:16149161 | G | A | 2 | a0001c0001t0001g0067 a0001c0001t0001g0068 |
2 | HG02071.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.154-114C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 2/16 | chr1 | 16149161 | |||||||
| chr1:16149185 | C | T | 2 | a0001c0004t0001g0184 a0001c0004t0001g0198 |
2 | NA19043.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.154-138G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 2/16 | chr1 | 16149185 | |||||||
| chr1:16149247 | T | C | 1 | a0001c0005t0001g0137 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.154-200A>G | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 2/16 | chr1 | 16149247 | |||||||
| chr1:16149252 | G | A | 1 | a0001c0001t0001g0207 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.154-205C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 2/16 | chr1 | 16149252 | |||||||
| chr1:16149318 | G | C | 9 | a0001c0001t0001g0204 a0001c0001t0001g0207 a0001c0002t0001g0202 others(6): Show |
9 | HG01106.hp1 HG01167.hp1 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.154-271C>G | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 2/16 | chr1 | 16149318 | |||||||
| chr1:16149385 | G | T | 1 | a0001c0004t0001g0106 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.154-338C>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 2/16 | chr1 | 16149385 | |||||||
| chr1:16149460 | G | A | 1 | a0001c0004t0001g0106 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.154-413C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 2/16 | chr1 | 16149460 | |||||||
| chr1:16149509 | C | T | 1 | a0002c0035t0003g0200 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.154-462G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 2/16 | chr1 | 16149509 | |||||||
| chr1:16149517 | T | C | 1 | a0001c0027t0001g0199 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.154-470A>G | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 2/16 | chr1 | 16149517 | |||||||
| chr1:16149563 | T | G | 1 | a0001c0026t0001g0138 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.154-516A>C | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 2/16 | chr1 | 16149563 | |||||||
| chr1:16149601 | A | G | 1 | a0001c0001t0001g0141 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.154-554T>C | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 2/16 | chr1 | 16149601 | |||||||
| chr1:16149748 | C | T | 3 | a0001c0002t0002g0029 a0001c0002t0002g0092 a0001c0002t0002g0093 |
4 | HG00733.hp2 HG01074.hp1 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.154-701G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 2/16 | chr1 | 16149748 | |||||||
| chr1:16149913 | A | G | 1 | a0001c0006t0001g0116 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.154-866T>C | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 2/16 | chr1 | 16149913 | |||||||
| chr1:16149938 | A | G | 2 | a0002c0008t0003g0112 a0002c0008t0003g0113 |
2 | HG02717.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.154-891T>C | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 2/16 | chr1 | 16149938 | |||||||
| chr1:16149965 | G | A | 1 | a0001c0034t0001g0217 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.154-918C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 2/16 | chr1 | 16149965 | |||||||
| chr1:16150002 | C | T | 6 | a0001c0001t0001g0111 a0001c0004t0002g0032 a0001c0004t0002g0107 others(3): Show |
9 | HG02451.hp1 HG02572.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.153+894G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 2/16 | chr1 | 16150002 | |||||||
| chr1:16150125 | C | T | 1 | a0001c0002t0001g0091 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.153+771G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 2/16 | chr1 | 16150125 | |||||||
| chr1:16150186 | C | T | 1 | a0001c0004t0001g0106 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.153+710G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 2/16 | chr1 | 16150186 | |||||||
| chr1:16150271 | G | A | 8 | a0001c0001t0001g0204 a0001c0001t0001g0207 a0001c0002t0001g0050 others(5): Show |
8 | HG01106.hp1 HG01167.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.153+625C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 2/16 | chr1 | 16150271 | |||||||
| chr1:16150329 | C | T | 9 | a0001c0001t0001g0204 a0001c0001t0001g0207 a0001c0002t0001g0050 others(6): Show |
9 | HG01106.hp1 HG01167.hp1 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.153+567G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 2/16 | chr1 | 16150329 | |||||||
| chr1:16150768 | G | A | 2 | a0002c0008t0003g0112 a0002c0008t0003g0113 |
2 | HG02717.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.153+128C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 2/16 | chr1 | 16150768 | |||||||
| chr1:16150810 | C | T | 1 | a0001c0001t0001g0072 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.153+86G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 2/16 | chr1 | 16150810 | |||||||
| chr1:16151515 | GGTA | G | 7 | a0001c0002t0001g0210 a0001c0004t0001g0009 a0001c0004t0001g0024 others(4): Show |
13 | HG01884.hp2 HG01891.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.86-555_86-553delTA others(1): Show |
EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 1/16 | chr1 | 16151515 | |||||||
| chr1:16151578 | G | A | 1 | a0001c0005t0001g0139 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.86-615C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 1/16 | chr1 | 16151578 | |||||||
| chr1:16151594 | T | C | 1 | a0001c0001t0001g0176 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.86-631A>G | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 1/16 | chr1 | 16151594 | |||||||
| chr1:16151621 | G | T | 1 | a0006c0013t0003g0081 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.86-658C>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 1/16 | chr1 | 16151621 | |||||||
| chr1:16151835 | T | C | 1 | a0001c0001t0001g0111 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.86-872A>G | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 1/16 | chr1 | 16151835 | |||||||
| chr1:16151837 | C | T | 1 | a0007c0022t0001g0218 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.86-874G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 1/16 | chr1 | 16151837 | |||||||
| chr1:16151949 | A | C | 1 | a0001c0006t0001g0115 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.86-986T>G | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 1/16 | chr1 | 16151949 | |||||||
| chr1:16151966 | A | C | 192 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(189): Show |
282 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(279): Show |
intron_variant | MODIFIER | c.86-1003T>G | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 1/16 | chr1 | 16151966 | |||||||
| chr1:16152022 | A | G | 5 | a0001c0004t0001g0009 a0001c0004t0001g0140 a0001c0004t0001g0213 others(2): Show |
9 | HG01891.hp2 HG02257.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.86-1059T>C | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 1/16 | chr1 | 16152022 | |||||||
| chr1:16152072 | C | T | 10 | a0001c0001t0001g0204 a0001c0001t0001g0207 a0001c0002t0001g0050 others(7): Show |
10 | HG01106.hp1 HG01167.hp1 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.86-1109G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 1/16 | chr1 | 16152072 | |||||||
| chr1:16152159 | C | T | 111 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(108): Show |
172 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(169): Show |
intron_variant | MODIFIER | c.86-1196G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 1/16 | chr1 | 16152159 | |||||||
| chr1:16152438 | G | C | 1 | a0001c0034t0001g0217 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.86-1475C>G | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 1/16 | chr1 | 16152438 | |||||||
| chr1:16152686 | T | C | 192 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(189): Show |
282 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(279): Show |
intron_variant | MODIFIER | c.86-1723A>G | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 1/16 | chr1 | 16152686 | |||||||
| chr1:16152822 | G | A | 1 | a0001c0004t0001g0213 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.86-1859C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 1/16 | chr1 | 16152822 | |||||||
| chr1:16152905 | C | T | 1 | a0001c0004t0001g0184 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.86-1942G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 1/16 | chr1 | 16152905 | |||||||
| chr1:16152951 | G | A | 1 | a0001c0003t0001g0177 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.86-1988C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 1/16 | chr1 | 16152951 | |||||||
| chr1:16153010 | T | C | 130 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(127): Show |
194 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(191): Show |
intron_variant | MODIFIER | c.86-2047A>G | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 1/16 | chr1 | 16153010 | |||||||
| chr1:16153041 | G | A | 1 | a0001c0001t0001g0178 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.86-2078C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 1/16 | chr1 | 16153041 | |||||||
| chr1:16153130 | GA | G | 167 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(164): Show |
253 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.86-2168delT | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 1/16 | chr1 | 16153130 | |||||||
| chr1:16153131 | A | G | 1 | a0001c0004t0002g0108 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.86-2168T>C | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 1/16 | chr1 | 16153131 | |||||||
| chr1:16153257 | G | C | 8 | a0001c0001t0001g0085 a0001c0002t0001g0028 a0001c0002t0001g0080 others(5): Show |
9 | HG01069.hp1 HG01071.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.86-2294C>G | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 1/16 | chr1 | 16153257 | |||||||
| chr1:16153435 | C | T | 1 | a0001c0001t0001g0071 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.85+2413G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 1/16 | chr1 | 16153435 | |||||||
| chr1:16153687 | G | C | 1 | a0002c0035t0003g0200 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.85+2161C>G | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 1/16 | chr1 | 16153687 | |||||||
| chr1:16153928 | T | C | 1 | a0001c0002t0001g0183 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.85+1920A>G | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 1/16 | chr1 | 16153928 | |||||||
| chr1:16153977 | C | G | 1 | a0001c0002t0001g0202 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.85+1871G>C | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 1/16 | chr1 | 16153977 | |||||||
| chr1:16153977 | C | T | 8 | a0001c0001t0001g0085 a0001c0002t0001g0028 a0001c0002t0001g0080 others(5): Show |
9 | HG01069.hp1 HG01071.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.85+1871G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 1/16 | chr1 | 16153977 | |||||||
| chr1:16154293 | T | C | 2 | a0002c0035t0003g0200 a0009c0029t0001g0114 |
2 | HG01891.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.85+1555A>G | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 1/16 | chr1 | 16154293 | |||||||
| chr1:16154374 | G | A | 2 | a0001c0001t0001g0012 a0001c0010t0001g0070 |
4 | HG01243.hp1 HG01952.hp1 HG01975.hp1 others(1): Show |
intron_variant | MODIFIER | c.85+1474C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 1/16 | chr1 | 16154374 | |||||||
| chr1:16154502 | G | C | 19 | a0001c0001t0001g0204 a0001c0001t0001g0207 a0001c0001t0001g0212 others(16): Show |
25 | HG01106.hp1 HG01167.hp1 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.85+1346C>G | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 1/16 | chr1 | 16154502 | |||||||
| chr1:16154513 | G | T | 1 | a0001c0002t0001g0080 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.85+1335C>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 1/16 | chr1 | 16154513 | |||||||
| chr1:16154656 | T | C | 1 | a0001c0004t0001g0184 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.85+1192A>G | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 1/16 | chr1 | 16154656 | |||||||
| chr1:16154756 | C | CA | 126 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(123): Show |
202 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.85+1091dupT | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 1/16 | chr1 | 16154756 | |||||||
| chr1:16154756 | C | CAA | 26 | a0001c0001t0001g0023 a0001c0001t0001g0027 a0001c0001t0001g0071 others(23): Show |
29 | HG00597.hp1 HG00597.hp2 HG00621.hp2 others(26): Show |
intron_variant | MODIFIER | c.85+1090_85+1091dup others(2): Show |
EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 1/16 | chr1 | 16154756 | |||||||
| chr1:16154756 | CA | C | 16 | a0001c0001t0001g0085 a0001c0001t0001g0212 a0001c0002t0001g0028 others(13): Show |
23 | HG01069.hp1 HG01071.hp2 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.85+1091delT | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 1/16 | chr1 | 16154756 | |||||||
| chr1:16154756 | CAA | C | 8 | a0001c0001t0001g0204 a0001c0001t0001g0207 a0001c0002t0001g0050 others(5): Show |
8 | HG01106.hp1 HG01167.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.85+1090_85+1091del others(2): Show |
EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 1/16 | chr1 | 16154756 | |||||||
| chr1:16154756 | CAAAAAAA others(4): Show |
C | 2 | a0001c0001t0001g0079 a0001c0003t0001g0013 |
4 | HG02738.hp1 HG03704.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.85+1081_85+1091del others(11): Show |
EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 1/16 | chr1 | 16154756 | |||||||
| chr1:16154847 | G | A | 1 | a0001c0015t0001g0201 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.85+1001C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 1/16 | chr1 | 16154847 | |||||||
| chr1:16154871 | C | T | 36 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(33): Show |
49 | HG00558.hp1 HG00597.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.85+977G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 1/16 | chr1 | 16154871 | |||||||
| chr1:16154991 | G | A | 19 | a0001c0001t0001g0204 a0001c0001t0001g0207 a0001c0001t0001g0212 others(16): Show |
25 | HG01106.hp1 HG01167.hp1 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.85+857C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 1/16 | chr1 | 16154991 | |||||||
| chr1:16155249 | G | A | 1 | a0001c0001t0001g0216 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.85+599C>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 1/16 | chr1 | 16155249 | |||||||
| chr1:16155395 | C | T | 1 | a0001c0002t0001g0050 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.85+453G>A | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 1/16 | chr1 | 16155395 | |||||||
| chr1:16155497 | C | A | 1 | a0001c0034t0001g0217 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.85+351G>T | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 1/16 | chr1 | 16155497 | |||||||
| chr1:16155670 | A | G | 1 | a0001c0002t0002g0049 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.85+178T>C | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 1/16 | chr1 | 16155670 | |||||||
| chr1:16155675 | C | G | 3 | a0001c0004t0001g0046 a0001c0004t0001g0047 a0001c0032t0001g0048 |
3 | HG00642.hp2 HG02976.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.85+173G>C | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 1/16 | chr1 | 16155675 | |||||||
| chr1:16155769 | T | C | 1 | a0007c0022t0001g0218 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.85+79A>G | EPHA2 | ENSG00000142627.13 | transcript | ENST00000358432.8 | protein_coding | 1/16 | chr1 | 16155769 |