Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 79180 |
| ensemblid | ENSG00000142634.13 |
| hgncid | 28670 |
| symbol | EFHD2 |
| name | EF-hand domain family member D2 |
| refseq_nuc | NM_024329.6 |
| refseq_prot | NP_077305.2 |
| ensembl_nuc | ENST00000375980.9 |
| ensembl_prot | ENSP00000365147.4 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 15409888 |
| end | 15430339 |
| strand | + |
| ver | v1.2 |
| region | chr1:15409888-15430339 |
| region5000 | chr1:15404888-15435339 |
| regionname0 | EFHD2_chr1_15409888_15430339 |
| regionname5000 | EFHD2_chr1_15404888_15435339 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 240 | 422 | 99 | 86 | 173 | 16 | 46 | 126 | EFHD2_chr1_15404888_15435339 | EFHD2 | MATDE others(235): Show |
chr1 | 15404888 | 15435339 |
| a0002 | 0/0 | 240 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | MATDE others(235): Show |
chr1 | 15404888 | 15435339 |
| a0003 | 0/0 | 240 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | MATDE others(235): Show |
chr1 | 15404888 | 15435339 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 720 | 404 | 84 | 83 | 173 | 16 | 46 | EFHD2_chr1_15404888_15435339 | EFHD2 | ATGGC others(715): Show |
chr1 | 15404888 | 15435339 | ||
| a0001c0002 | 0/0 | 720 | 18 | 15 | 3 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | ATGGC others(715): Show |
chr1 | 15404888 | 15435339 | ||
| a0002c0003 | 0/0 | 720 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | ATGGC others(715): Show |
chr1 | 15404888 | 15435339 | ||
| a0003c0004 | 0/0 | 720 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | ATGGC others(715): Show |
chr1 | 15404888 | 15435339 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 2422 | 226 | 47 | 42 | 100 | 13 | 23 | EFHD2_chr1_15404888_15435339 | EFHD2 | GAGTG others(2417): Show |
chr1 | 15404888 | 15435339 |
| a0001c0001t0002 | 0/0 | 2422 | 67 | 12 | 20 | 27 | 1 | 7 | EFHD2_chr1_15404888_15435339 | EFHD2 | GAGTG others(2417): Show |
chr1 | 15404888 | 15435339 |
| a0001c0001t0003 | 0/1 | 2422 | 63 | 3 | 8 | 36 | 1 | 14 | EFHD2_chr1_15404888_15435339 | EFHD2 | GAGTG others(2417): Show |
chr1 | 15404888 | 15435339 |
| a0001c0001t0004 | 0/0 | 2422 | 7 | 0 | 7 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | GAGTG others(2417): Show |
chr1 | 15404888 | 15435339 |
| a0001c0001t0005 | 0/0 | 2422 | 6 | 5 | 1 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | GAGTG others(2417): Show |
chr1 | 15404888 | 15435339 |
| a0001c0001t0006 | 0/0 | 2422 | 7 | 0 | 0 | 7 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | GAGTG others(2417): Show |
chr1 | 15404888 | 15435339 |
| a0001c0001t0007 | 0/0 | 2422 | 2 | 1 | 1 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | GAGTG others(2417): Show |
chr1 | 15404888 | 15435339 |
| a0001c0001t0008 | 0/0 | 2422 | 6 | 6 | 0 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | GAGTG others(2417): Show |
chr1 | 15404888 | 15435339 |
| a0001c0001t0009 | 0/0 | 2422 | 3 | 1 | 2 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | GAGTG others(2417): Show |
chr1 | 15404888 | 15435339 |
| a0001c0001t0011 | 0/0 | 2422 | 3 | 3 | 0 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | GAGTG others(2417): Show |
chr1 | 15404888 | 15435339 |
| a0001c0001t0012 | 0/0 | 2422 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | GAGTG others(2417): Show |
chr1 | 15404888 | 15435339 |
| a0001c0001t0013 | 0/0 | 2422 | 1 | 0 | 0 | 0 | 1 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | GAGTG others(2417): Show |
chr1 | 15404888 | 15435339 |
| a0001c0001t0014 | 0/0 | 2422 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | GAGTG others(2417): Show |
chr1 | 15404888 | 15435339 |
| a0001c0001t0015 | 0/0 | 2422 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | GAGTG others(2417): Show |
chr1 | 15404888 | 15435339 |
| a0001c0001t0016 | 0/0 | 2422 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | GAGTG others(2417): Show |
chr1 | 15404888 | 15435339 |
| a0001c0001t0017 | 0/0 | 2422 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | GAGTG others(2417): Show |
chr1 | 15404888 | 15435339 |
| a0001c0001t0018 | 0/0 | 2422 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | GAGTG others(2417): Show |
chr1 | 15404888 | 15435339 |
| a0001c0001t0019 | 0/0 | 2422 | 1 | 0 | 1 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | GAGTG others(2417): Show |
chr1 | 15404888 | 15435339 |
| a0001c0001t0020 | 0/0 | 2422 | 1 | 0 | 0 | 0 | 0 | 1 | EFHD2_chr1_15404888_15435339 | EFHD2 | GAGTG others(2417): Show |
chr1 | 15404888 | 15435339 |
| a0001c0001t0021 | 0/0 | 2422 | 1 | 0 | 0 | 0 | 0 | 1 | EFHD2_chr1_15404888_15435339 | EFHD2 | GAGTG others(2417): Show |
chr1 | 15404888 | 15435339 |
| a0001c0001t0022 | 0/0 | 2422 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | GAGTG others(2417): Show |
chr1 | 15404888 | 15435339 |
| a0001c0001t0023 | 0/0 | 2422 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | GAGTG others(2417): Show |
chr1 | 15404888 | 15435339 |
| a0001c0001t0024 | 0/0 | 2422 | 1 | 0 | 1 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | GAGTG others(2417): Show |
chr1 | 15404888 | 15435339 |
| a0001c0001t0025 | 0/0 | 2422 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | GAGTG others(2417): Show |
chr1 | 15404888 | 15435339 |
| a0001c0002t0001 | 0/0 | 2422 | 7 | 7 | 0 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | GAGTG others(2417): Show |
chr1 | 15404888 | 15435339 |
| a0001c0002t0005 | 0/0 | 2422 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | GAGTG others(2417): Show |
chr1 | 15404888 | 15435339 |
| a0001c0002t0007 | 0/0 | 2422 | 4 | 4 | 0 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | GAGTG others(2417): Show |
chr1 | 15404888 | 15435339 |
| a0001c0002t0009 | 0/0 | 2422 | 2 | 1 | 1 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | GAGTG others(2417): Show |
chr1 | 15404888 | 15435339 |
| a0001c0002t0010 | 0/0 | 2422 | 4 | 2 | 2 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | GAGTG others(2417): Show |
chr1 | 15404888 | 15435339 |
| a0002c0003t0001 | 0/0 | 2422 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | GAGTG others(2417): Show |
chr1 | 15404888 | 15435339 |
| a0003c0004t0001 | 0/0 | 2422 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | GAGTG others(2417): Show |
chr1 | 15404888 | 15435339 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0002 | 0/0 | 8 | 0 | 1 | 7 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0003 | 0/0 | 9 | 0 | 0 | 8 | 0 | 1 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0004 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0005 | 1/0 | 7 | 0 | 3 | 0 | 1 | 2 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0006 | 0/0 | 5 | 0 | 1 | 3 | 0 | 1 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0007 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0015 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0043 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0002g0008 | 0/0 | 5 | 0 | 2 | 2 | 0 | 1 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0002g0013 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0002g0024 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0002g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0002g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0002g0035 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0002g0036 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0002g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0002g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0002g0049 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0002g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0002g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0002g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0002g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0002g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0002g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0002g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0002g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0002g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0002g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0002g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0002g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0003g0001 | 0/0 | 11 | 1 | 0 | 10 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0003g0011 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0003g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0003g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0003g0016 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0003g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0003g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0003g0027 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0003g0031 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0003g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0003g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0003g0047 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0003g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0003g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0003g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0003g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0003g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0003g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0003g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0003g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0003g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0003g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0003g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0003g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0003g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0003g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0003g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0003g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0003g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0003g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0003g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0003g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0003g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0003g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0003g0294 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0003g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0003g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0004g0021 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0004g0040 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0004g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0004g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0005g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0005g0052 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0005g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0005g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0005g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0006g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0006g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0006g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0006g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0006g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0007g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0007g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0008g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0008g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0008g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0008g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0008g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0009g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0009g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0009g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0011g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0011g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0011g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0012g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0013g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0014g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0015g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0016g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0017g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0018g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0019g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0020g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0021g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0022g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0023g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0024g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0001t0025g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0002t0001g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0002t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0002t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0002t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0002t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0002t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0002t0005g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0002t0007g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0002t0007g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0002t0007g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0002t0007g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0002t0009g0034 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0002t0010g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0002t0010g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0002t0010g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0001c0002t0010g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0002c0003t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| a0003c0004t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0216 | EUR | GBR | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0153 | EUR | GBR | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0135 | EUR | GBR | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0030 | EUR | GBR | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG00280 | hp1 | a0001 | c0001 | t0003 | g0171 | EUR | FIN | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0182 | EUR | FIN | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | FIN | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0208 | EUR | FIN | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG00408 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | CHS | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG00423 | hp1 | a0001 | c0001 | t0003 | g0114 | EAS | CHS | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | CHS | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | CHS | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | CHS | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG00544 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | CHS | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG00544 | hp2 | a0001 | c0001 | t0003 | g0047 | EAS | CHS | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | CHS | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG00558 | hp2 | a0001 | c0001 | t0006 | g0166 | EAS | CHS | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | CHS | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG00597 | hp2 | a0001 | c0001 | t0003 | g0012 | EAS | CHS | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG00621 | hp1 | a0001 | c0001 | t0003 | g0108 | EAS | CHS | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | CHS | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG00639 | hp1 | a0001 | c0001 | t0004 | g0170 | AMR | PUR | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG00639 | hp2 | a0001 | c0001 | t0003 | g0181 | AMR | PUR | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0035 | AMR | PUR | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG00642 | hp2 | a0001 | c0001 | t0019 | g0240 | AMR | PUR | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG00673 | hp1 | a0001 | c0001 | t0003 | g0113 | EAS | CHS | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0167 | AMR | PUR | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0213 | AMR | PUR | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0203 | AMR | PUR | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG00735 | hp2 | a0001 | c0001 | t0003 | g0223 | AMR | PUR | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0297 | AMR | PUR | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG00738 | hp2 | a0001 | c0001 | t0024 | g0224 | AMR | PUR | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | PUR | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0296 | AMR | PUR | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG01069 | hp2 | a0001 | c0002 | t0010 | g0227 | AMR | PUR | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0242 | AMR | PUR | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0290 | AMR | PUR | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG01071 | hp2 | a0001 | c0002 | t0010 | g0226 | AMR | PUR | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0269 | AMR | PUR | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0238 | AMR | PUR | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0071 | AMR | PUR | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0288 | AMR | PUR | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0066 | AMR | PUR | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0032 | AMR | PUR | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG01106 | hp2 | a0001 | c0001 | t0009 | g0116 | AMR | PUR | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0272 | AMR | PUR | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG01109 | hp2 | a0001 | c0001 | t0009 | g0234 | AMR | PUR | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG01167 | hp2 | a0001 | c0001 | t0007 | g0094 | AMR | PUR | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0013 | AMR | PUR | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0013 | AMR | PUR | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0197 | AMR | PUR | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0183 | AMR | PUR | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0032 | AMR | PUR | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG01192 | hp2 | a0001 | c0001 | t0004 | g0021 | AMR | PUR | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG01243 | hp2 | a0001 | c0001 | t0005 | g0298 | AMR | PUR | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0049 | AMR | CLM | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG01256 | hp1 | a0001 | c0001 | t0004 | g0040 | AMR | CLM | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0212 | AMR | CLM | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0028 | AMR | CLM | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG01257 | hp2 | a0001 | c0002 | t0009 | g0034 | AMR | CLM | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0028 | AMR | CLM | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0211 | AMR | CLM | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0049 | AMR | CLM | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0196 | AMR | CLM | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG01346 | hp2 | a0001 | c0001 | t0003 | g0059 | AMR | CLM | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | CLM | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | CLM | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0013 | AMR | CLM | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0180 | AMR | CLM | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | CLM | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG01496 | hp2 | a0001 | c0001 | t0003 | g0011 | AMR | CLM | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0145 | EUR | IBS | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0268 | EUR | IBS | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG01516 | hp1 | a0001 | c0001 | t0013 | g0084 | EUR | IBS | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0189 | EUR | IBS | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0300 | AFR | ACB | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG01891 | hp1 | a0001 | c0002 | t0001 | g0044 | AFR | ACB | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG01891 | hp2 | a0001 | c0001 | t0005 | g0052 | AFR | ACB | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0201 | AMR | PEL | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PEL | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG01934 | hp2 | a0001 | c0001 | t0003 | g0011 | AMR | PEL | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG01943 | hp1 | a0001 | c0001 | t0003 | g0304 | AMR | PEL | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0215 | AMR | PEL | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0008 | AMR | PEL | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG01952 | hp2 | a0001 | c0001 | t0004 | g0110 | AMR | PEL | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | PEL | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0267 | AMR | PEL | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0218 | AMR | PEL | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | PEL | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | PEL | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0008 | AMR | PEL | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0176 | AMR | PEL | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG01993 | hp2 | a0001 | c0001 | t0004 | g0021 | AMR | PEL | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG02004 | hp1 | a0001 | c0001 | t0003 | g0025 | AMR | PEL | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG02015 | hp1 | a0002 | c0003 | t0001 | g0088 | EAS | KHV | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | KHV | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | KHV | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0303 | EAS | KHV | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | KHV | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG02055 | hp1 | a0001 | c0002 | t0001 | g0301 | AFR | ACB | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | ACB | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | KHV | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | KHV | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG02071 | hp1 | a0001 | c0001 | t0003 | g0011 | EAS | KHV | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG02071 | hp2 | a0001 | c0001 | t0006 | g0165 | EAS | KHV | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | KHV | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | KHV | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG02083 | hp2 | a0001 | c0001 | t0006 | g0002 | EAS | KHV | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG02129 | hp1 | a0001 | c0001 | t0006 | g0023 | EAS | KHV | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG02132 | hp1 | a0001 | c0001 | t0003 | g0115 | EAS | KHV | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | KHV | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | KHV | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | KHV | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG02145 | hp1 | a0001 | c0002 | t0007 | g0058 | AFR | ACB | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0248 | AFR | ACB | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0273 | EAS | CDX | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG02155 | hp2 | a0001 | c0001 | t0006 | g0009 | EAS | CDX | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | CDX | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG02257 | hp1 | a0001 | c0002 | t0001 | g0061 | AFR | ACB | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0256 | AFR | ACB | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | ACB | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | ACB | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG02273 | hp1 | a0001 | c0001 | t0004 | g0021 | AMR | PEL | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0173 | AMR | PEL | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG02280 | hp1 | a0001 | c0002 | t0007 | g0117 | AFR | ACB | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG02280 | hp2 | a0001 | c0001 | t0003 | g0031 | AFR | ACB | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG02293 | hp2 | a0001 | c0001 | t0003 | g0027 | AMR | PEL | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | PEL | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0207 | AFR | ACB | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0233 | AFR | ACB | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | KHV | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | KHV | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG02572 | hp1 | a0001 | c0001 | t0018 | g0118 | AFR | GWD | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG02572 | hp2 | a0001 | c0001 | t0009 | g0299 | AFR | GWD | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0188 | SAS | PJL | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG02602 | hp2 | a0001 | c0001 | t0003 | g0016 | SAS | PJL | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG02615 | hp1 | a0001 | c0001 | t0008 | g0260 | AFR | GWD | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0237 | AFR | GWD | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG02622 | hp1 | a0001 | c0002 | t0001 | g0258 | AFR | GWD | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG02622 | hp2 | a0001 | c0001 | t0003 | g0247 | AFR | GWD | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG02630 | hp1 | a0001 | c0002 | t0010 | g0225 | AFR | GWD | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | GWD | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0244 | AFR | GWD | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG02647 | hp2 | a0001 | c0002 | t0007 | g0063 | AFR | GWD | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG02683 | hp1 | a0001 | c0001 | t0003 | g0147 | SAS | PJL | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0035 | SAS | PJL | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0037 | SAS | PJL | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0184 | SAS | PJL | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0292 | AFR | GWD | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0261 | AFR | GWD | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0119 | AFR | GWD | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0042 | AFR | GWD | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0164 | SAS | PJL | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0163 | SAS | PJL | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG02738 | hp1 | a0001 | c0001 | t0003 | g0144 | SAS | PJL | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG02738 | hp2 | a0001 | c0001 | t0020 | g0205 | SAS | PJL | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0291 | AFR | GWD | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG02809 | hp2 | a0001 | c0001 | t0014 | g0289 | AFR | GWD | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | GWD | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0253 | AFR | GWD | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | GWD | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0062 | AFR | GWD | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | GWD | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0228 | AFR | GWD | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0241 | AFR | GWD | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG02896 | hp2 | a0001 | c0001 | t0008 | g0046 | AFR | GWD | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG02897 | hp1 | a0001 | c0001 | t0008 | g0046 | AFR | GWD | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | GWD | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG02922 | hp1 | a0003 | c0004 | t0001 | g0295 | AFR | ESN | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG02922 | hp2 | a0001 | c0001 | t0007 | g0095 | AFR | ESN | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | ESN | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG02965 | hp2 | a0001 | c0001 | t0005 | g0220 | AFR | ESN | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | ESN | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0239 | AFR | ESN | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG02976 | hp1 | a0001 | c0001 | t0005 | g0052 | AFR | ESN | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0243 | AFR | ESN | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0168 | SAS | PJL | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG03041 | hp1 | a0001 | c0001 | t0008 | g0246 | AFR | GWD | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | GWD | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | MSL | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0251 | AFR | MSL | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG03130 | hp1 | a0001 | c0002 | t0001 | g0057 | AFR | ESN | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG03130 | hp2 | a0001 | c0001 | t0015 | g0264 | AFR | ESN | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG03139 | hp1 | a0001 | c0001 | t0008 | g0255 | AFR | ESN | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0065 | AFR | ESN | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG03195 | hp1 | a0001 | c0001 | t0012 | g0232 | AFR | ESN | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0229 | AFR | ESN | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | MSL | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0230 | AFR | MSL | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0250 | AFR | MSL | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | MSL | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG03239 | hp1 | a0001 | c0001 | t0003 | g0107 | SAS | PJL | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG03239 | hp2 | a0001 | c0001 | t0003 | g0031 | SAS | PJL | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | MSL | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0262 | AFR | MSL | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | MSL | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0102 | AFR | MSL | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0123 | SAS | PJL | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0036 | SAS | PJL | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0036 | SAS | PJL | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG03516 | hp1 | a0001 | c0001 | t0005 | g0221 | AFR | ESN | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0245 | AFR | ESN | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG03540 | hp1 | a0001 | c0002 | t0007 | g0100 | AFR | GWD | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG03540 | hp2 | a0001 | c0001 | t0008 | g0259 | AFR | GWD | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0041 | AFR | MSL | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | MSL | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0156 | SAS | PJL | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0136 | SAS | PJL | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | STU | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | STU | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG03704 | hp1 | a0001 | c0001 | t0003 | g0047 | SAS | PJL | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG03704 | hp2 | a0001 | c0001 | t0003 | g0016 | SAS | PJL | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0086 | SAS | PJL | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG03710 | hp2 | a0001 | c0001 | t0003 | g0122 | SAS | PJL | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0081 | SAS | BEB | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0078 | SAS | BEB | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0037 | SAS | BEB | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0204 | SAS | BEB | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0219 | SAS | BEB | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG03927 | hp2 | a0001 | c0001 | t0003 | g0091 | SAS | BEB | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG03942 | hp1 | a0001 | c0001 | t0021 | g0014 | SAS | BEB | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0029 | SAS | BEB | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG04115 | hp1 | a0001 | c0001 | t0003 | g0186 | SAS | STU | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0053 | SAS | STU | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0195 | SAS | BEB | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG04184 | hp2 | a0001 | c0001 | t0003 | g0187 | SAS | BEB | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG04199 | hp1 | a0001 | c0001 | t0003 | g0016 | SAS | STU | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0093 | SAS | STU | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0008 | SAS | STU | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG04204 | hp2 | a0001 | c0001 | t0003 | g0148 | SAS | STU | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0151 | SAS | STU | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG04228 | hp2 | a0001 | c0001 | t0003 | g0014 | SAS | STU | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA18522 | hp1 | a0001 | c0001 | t0011 | g0257 | AFR | YRI | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA18522 | hp2 | a0001 | c0001 | t0011 | g0254 | AFR | YRI | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | CHB | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0271 | EAS | CHB | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA18747 | hp1 | a0001 | c0001 | t0003 | g0033 | EAS | CHB | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | CHB | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0249 | AFR | YRI | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA18906 | hp2 | a0001 | c0001 | t0016 | g0068 | AFR | YRI | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA18939 | hp1 | a0001 | c0001 | t0003 | g0039 | EAS | JPT | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA18940 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA18940 | hp2 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0150 | EAS | JPT | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA18941 | hp2 | a0001 | c0001 | t0003 | g0126 | EAS | JPT | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA18943 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA18952 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA18953 | hp1 | a0001 | c0001 | t0022 | g0124 | EAS | JPT | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA18954 | hp1 | a0001 | c0001 | t0003 | g0027 | EAS | JPT | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA18956 | hp1 | a0001 | c0001 | t0003 | g0190 | EAS | JPT | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA18956 | hp2 | a0001 | c0001 | t0002 | g0287 | EAS | JPT | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA18960 | hp2 | a0001 | c0001 | t0003 | g0305 | EAS | JPT | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA18961 | hp1 | a0001 | c0001 | t0003 | g0134 | EAS | JPT | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA18964 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA18968 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA18970 | hp2 | a0001 | c0001 | t0006 | g0009 | EAS | JPT | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA18971 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA18971 | hp2 | a0001 | c0001 | t0017 | g0006 | EAS | JPT | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA18975 | hp1 | a0001 | c0001 | t0003 | g0179 | EAS | JPT | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA18979 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA18980 | hp1 | a0001 | c0001 | t0003 | g0039 | EAS | JPT | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0194 | EAS | JPT | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA18983 | hp2 | a0001 | c0001 | t0003 | g0019 | EAS | JPT | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0266 | EAS | JPT | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0283 | EAS | JPT | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA18990 | hp1 | a0001 | c0001 | t0006 | g0023 | EAS | JPT | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA18990 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0284 | EAS | JPT | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA18991 | hp2 | a0001 | c0001 | t0002 | g0200 | EAS | JPT | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA18995 | hp1 | a0001 | c0001 | t0003 | g0191 | EAS | JPT | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0128 | EAS | JPT | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0285 | EAS | JPT | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0280 | EAS | JPT | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA19002 | hp1 | a0001 | c0001 | t0003 | g0278 | EAS | JPT | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA19003 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA19006 | hp2 | a0001 | c0001 | t0003 | g0198 | EAS | JPT | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA19011 | hp1 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA19030 | hp1 | a0001 | c0002 | t0001 | g0044 | AFR | LWK | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0293 | AFR | LWK | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA19043 | hp1 | a0001 | c0001 | t0003 | g0001 | AFR | LWK | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0236 | AFR | LWK | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA19055 | hp2 | a0001 | c0001 | t0003 | g0109 | EAS | JPT | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0143 | EAS | JPT | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA19057 | hp1 | a0001 | c0001 | t0003 | g0019 | EAS | JPT | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA19060 | hp1 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA19068 | hp2 | a0001 | c0001 | t0023 | g0012 | EAS | JPT | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA19090 | hp1 | a0001 | c0001 | t0003 | g0089 | EAS | JPT | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0140 | EAS | JPT | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA19240 | hp1 | a0001 | c0002 | t0001 | g0064 | AFR | YRI | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | YRI | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | ASW | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | ASW | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0169 | EUR | TSI | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0160 | EUR | TSI | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0072 | EUR | TSI | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0073 | EUR | TSI | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | CLM | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG01123 | hp2 | a0001 | c0001 | t0004 | g0040 | AMR | CLM | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG02109 | hp1 | a0001 | c0001 | t0005 | g0051 | AFR | ACB | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG02109 | hp2 | a0001 | c0001 | t0011 | g0252 | AFR | ACB | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG02486 | hp1 | a0001 | c0002 | t0005 | g0060 | AFR | ACB | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | ACB | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG02559 | hp1 | a0001 | c0002 | t0009 | g0034 | AFR | ACB | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0222 | AFR | ACB | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | MSL | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | MSL | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0041 | AFR | USA | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| HG06807 | hp2 | a0001 | c0001 | t0025 | g0231 | AFR | USA | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | USA | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0263 | AFR | USA | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | LWK | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| NA21309 | hp2 | a0001 | c0002 | t0010 | g0235 | AFR | LWK | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0003 | g0294 | REF | REF | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0005 | REF | REF | EFHD2_chr1_15404888_15435339 | EFHD2 | chr1 | 15404888 | 15435339 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:15410105 | C | T | 1 | a0003 | 1 | HG02922.hp1 | missense_variant | MODERATE | c.134C>T | p.Ala45Val | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/4 | 218/2422 | 134/723 | 45/240 | chr1 | 15410105 | |||
| chr1:15410270 | T | C | 1 | a0002 | 1 | HG02015.hp1 | missense_variant | MODERATE | c.299T>C | p.Met100Thr | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/4 | 383/2422 | 299/723 | 100/240 | chr1 | 15410270 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:15425883 | G | A | 1 | a0001c0002 | 18 | HG01069.hp2 HG01071.hp2 HG01257.hp2 others(15): Show |
synonymous_variant | LOW | c.321G>A | p.Gly107Gly | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 2/4 | 405/2422 | 321/723 | 107/240 | chr1 | 15425883 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:15409947 | C | G | 1 | a0001c0001t0025 | 1 | HG06807.hp2 | 5_prime_UTR_variant | MODIFIER | c.-25C>G | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/4 | 25 | chr1 | 15409947 | ||||||
| chr1:15428725 | C | T | 2 | a0001c0001t0008 a0001c0002t0010 |
10 | HG01069.hp2 HG01071.hp2 HG02615.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1C>T | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 4/4 | 1 | chr1 | 15428725 | ||||||
| chr1:15428729 | G | A | 2 | a0001c0001t0008 a0001c0002t0010 |
10 | HG01069.hp2 HG01071.hp2 HG02615.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*5G>A | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 4/4 | 5 | chr1 | 15428729 | ||||||
| chr1:15428752 | C | T | 5 | a0001c0001t0003 a0001c0001t0021 a0001c0001t0022 others(2): Show |
66 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(63): Show |
3_prime_UTR_variant | MODIFIER | c.*28C>T | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 4/4 | 28 | chr1 | 15428752 | ||||||
| chr1:15429001 | C | T | 1 | a0001c0001t0020 | 1 | HG02738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*277C>T | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 4/4 | 277 | chr1 | 15429001 | ||||||
| chr1:15429054 | A | G | 1 | a0001c0001t0019 | 1 | HG00642.hp2 | 3_prime_UTR_variant | MODIFIER | c.*330A>G | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 4/4 | 330 | chr1 | 15429054 | ||||||
| chr1:15429101 | A | G | 1 | a0001c0001t0018 | 1 | HG02572.hp1 | 3_prime_UTR_variant | MODIFIER | c.*377A>G | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 4/4 | 377 | chr1 | 15429101 | ||||||
| chr1:15429171 | C | A | 1 | a0001c0001t0021 | 1 | HG03942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*447C>A | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 4/4 | 447 | chr1 | 15429171 | ||||||
| chr1:15429180 | G | A | 8 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0011 others(5): Show |
82 | HG00639.hp1 HG00642.hp1 HG00642.hp2 others(79): Show |
3_prime_UTR_variant | MODIFIER | c.*456G>A | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 4/4 | 456 | chr1 | 15429180 | ||||||
| chr1:15429232 | A | T | 2 | a0001c0001t0024 a0001c0002t0010 |
5 | HG00738.hp2 HG01069.hp2 HG01071.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*508A>T | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 4/4 | 508 | chr1 | 15429232 | ||||||
| chr1:15429279 | C | T | 1 | a0001c0001t0023 | 1 | NA19068.hp2 | 3_prime_UTR_variant | MODIFIER | c.*555C>T | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 4/4 | 555 | chr1 | 15429279 | ||||||
| chr1:15429306 | G | C | 1 | a0001c0001t0004 | 7 | HG00639.hp1 HG01123.hp2 HG01192.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*582G>C | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 4/4 | 582 | chr1 | 15429306 | ||||||
| chr1:15429306 | G | T | 1 | a0001c0001t0017 | 1 | NA18971.hp2 | 3_prime_UTR_variant | MODIFIER | c.*582G>T | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 4/4 | 582 | chr1 | 15429306 | ||||||
| chr1:15429339 | C | T | 1 | a0001c0001t0016 | 1 | NA18906.hp2 | 3_prime_UTR_variant | MODIFIER | c.*615C>T | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 4/4 | 615 | chr1 | 15429339 | ||||||
| chr1:15429461 | C | T | 1 | a0001c0001t0013 | 1 | HG01516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*737C>T | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 4/4 | 737 | chr1 | 15429461 | ||||||
| chr1:15429515 | C | A | 3 | a0001c0001t0007 a0001c0001t0012 a0001c0002t0007 |
7 | HG01167.hp2 HG02145.hp1 HG02280.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*791C>A | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 4/4 | 791 | chr1 | 15429515 | ||||||
| chr1:15429622 | C | T | 1 | a0001c0001t0015 | 1 | HG03130.hp2 | 3_prime_UTR_variant | MODIFIER | c.*898C>T | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 4/4 | 898 | chr1 | 15429622 | ||||||
| chr1:15429713 | C | G | 1 | a0001c0001t0022 | 1 | NA18953.hp1 | 3_prime_UTR_variant | MODIFIER | c.*989C>G | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 4/4 | 989 | chr1 | 15429713 | ||||||
| chr1:15429742 | C | T | 1 | a0001c0001t0006 | 7 | HG00558.hp2 HG02071.hp2 HG02083.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1018C>T | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 4/4 | 1018 | chr1 | 15429742 | ||||||
| chr1:15429910 | C | T | 3 | a0001c0001t0009 a0001c0001t0011 a0001c0002t0009 |
8 | HG01106.hp2 HG01109.hp2 HG01257.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1186C>T | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 4/4 | 1186 | chr1 | 15429910 | ||||||
| chr1:15430064 | G | A | 1 | a0001c0001t0014 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1340G>A | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 4/4 | 1340 | chr1 | 15430064 | ||||||
| chr1:15430146 | G | A | 2 | a0001c0001t0005 a0001c0002t0005 |
7 | HG01243.hp2 HG01891.hp2 HG02109.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1422G>A | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 4/4 | 1422 | chr1 | 15430146 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:15410623 | G | A | 6 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0056 others(3): Show |
6 | HG02055.hp2 HG02145.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.308+344G>A | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15410623 | |||||||
| chr1:15410646 | G | A | 14 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0056 others(11): Show |
14 | HG01099.hp2 HG01346.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.308+367G>A | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15410646 | |||||||
| chr1:15411000 | C | G | 2 | a0001c0001t0003g0304 a0001c0001t0003g0305 |
2 | HG01943.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.308+721C>G | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15411000 | |||||||
| chr1:15411063 | T | C | 1 | a0001c0001t0001g0067 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.308+784T>C | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15411063 | |||||||
| chr1:15411071 | G | A | 1 | a0001c0001t0016g0068 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.308+792G>A | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15411071 | |||||||
| chr1:15411197 | G | A | 1 | a0001c0001t0001g0069 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.308+918G>A | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15411197 | |||||||
| chr1:15411324 | G | C | 36 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0017 others(33): Show |
46 | HG00423.hp2 HG00438.hp2 HG01081.hp1 others(43): Show |
intron_variant | MODIFIER | c.308+1045G>C | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15411324 | |||||||
| chr1:15411375 | C | T | 2 | a0001c0001t0001g0302 a0001c0001t0001g0303 |
2 | HG02027.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.308+1096C>T | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15411375 | |||||||
| chr1:15411432 | C | T | 7 | a0001c0001t0001g0051 a0001c0001t0002g0300 a0001c0001t0005g0051 others(4): Show |
8 | HG01243.hp2 HG01884.hp2 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.308+1153C>T | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15411432 | |||||||
| chr1:15411444 | C | T | 3 | a0001c0001t0007g0094 a0001c0001t0007g0095 a0001c0001t0016g0068 |
3 | HG01167.hp2 HG02922.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.308+1165C>T | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15411444 | |||||||
| chr1:15411481 | T | A | 1 | a0001c0001t0001g0096 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.308+1202T>A | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15411481 | |||||||
| chr1:15411556 | T | C | 44 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0017 others(41): Show |
55 | HG00423.hp2 HG00438.hp2 HG01081.hp1 others(52): Show |
intron_variant | MODIFIER | c.308+1277T>C | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15411556 | |||||||
| chr1:15411610 | G | GCC | 28 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0018 others(25): Show |
45 | HG00423.hp1 HG00621.hp1 HG00673.hp1 others(42): Show |
intron_variant | MODIFIER | c.308+1332_308+1333d others(4): Show |
EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 15411610 | ||||||
| chr1:15411719 | A | C | 1 | a0001c0001t0001g0069 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.308+1440A>C | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15411719 | |||||||
| chr1:15411869 | A | C | 2 | a0001c0001t0001g0296 a0001c0001t0001g0297 |
2 | HG00738.hp1 HG00741.hp2 |
intron_variant | MODIFIER | c.308+1590A>C | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15411869 | |||||||
| chr1:15412016 | A | G | 1 | a0003c0004t0001g0295 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.308+1737A>G | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15412016 | |||||||
| chr1:15412034 | C | G | 1 | a0001c0001t0003g0115 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.308+1755C>G | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15412034 | |||||||
| chr1:15412120 | C | T | 31 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0017 others(28): Show |
41 | HG00423.hp2 HG00438.hp2 HG01081.hp1 others(38): Show |
intron_variant | MODIFIER | c.308+1841C>T | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15412120 | |||||||
| chr1:15412165 | C | T | 58 | a0001c0001t0001g0015 a0001c0001t0001g0054 a0001c0001t0001g0055 others(55): Show |
72 | HG00438.hp1 HG00544.hp2 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.308+1886C>T | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15412165 | |||||||
| chr1:15412307 | G | A | 2 | a0001c0001t0009g0116 a0001c0002t0007g0117 |
2 | HG01106.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.308+2028G>A | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15412307 | |||||||
| chr1:15412383 | C | T | 2 | a0001c0001t0001g0023 a0001c0001t0006g0023 |
3 | HG02074.hp1 HG02129.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.308+2104C>T | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15412383 | |||||||
| chr1:15412409 | T | C | 2 | a0001c0001t0002g0119 a0001c0001t0018g0118 |
2 | HG02572.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.308+2130T>C | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15412409 | |||||||
| chr1:15412520 | A | G | 181 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0009 others(178): Show |
229 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(226): Show |
intron_variant | MODIFIER | c.308+2241A>G | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15412520 | |||||||
| chr1:15412579 | T | C | 1 | a0001c0001t0001g0120 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.308+2300T>C | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15412579 | |||||||
| chr1:15412592 | C | T | 1 | a0001c0001t0001g0288 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.308+2313C>T | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15412592 | |||||||
| chr1:15412737 | G | A | 31 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0017 others(28): Show |
41 | HG00423.hp2 HG00438.hp2 HG01081.hp1 others(38): Show |
intron_variant | MODIFIER | c.308+2458G>A | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15412737 | |||||||
| chr1:15412762 | G | C | 2 | a0001c0001t0005g0220 a0001c0001t0005g0221 |
2 | HG02965.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.308+2483G>C | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15412762 | |||||||
| chr1:15412766 | A | G | 6 | a0001c0001t0001g0253 a0001c0001t0001g0256 a0001c0001t0008g0255 others(3): Show |
6 | HG02109.hp2 HG02257.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.308+2487A>G | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15412766 | |||||||
| chr1:15412767 | C | G | 49 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0017 others(46): Show |
60 | HG00423.hp2 HG00438.hp2 HG01070.hp2 others(57): Show |
intron_variant | MODIFIER | c.308+2488C>G | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15412767 | |||||||
| chr1:15412808 | T | A | 2 | a0001c0001t0001g0071 a0001c0001t0001g0072 |
2 | HG01081.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.308+2529T>A | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15412808 | |||||||
| chr1:15412854 | C | A | 130 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0009 others(127): Show |
172 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(169): Show |
intron_variant | MODIFIER | c.308+2575C>A | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15412854 | |||||||
| chr1:15412865 | A | G | 1 | a0001c0001t0001g0219 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.308+2586A>G | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15412865 | |||||||
| chr1:15412884 | AC | A | 3 | a0001c0001t0001g0218 a0001c0001t0004g0021 a0001c0001t0004g0040 |
6 | HG01123.hp2 HG01192.hp2 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.308+2609delC | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 15412884 | ||||||
| chr1:15412891 | G | A | 13 | a0001c0001t0001g0042 a0001c0001t0001g0228 a0001c0001t0001g0229 others(10): Show |
14 | HG00735.hp2 HG00738.hp2 HG01069.hp2 others(11): Show |
intron_variant | MODIFIER | c.308+2612G>A | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15412891 | |||||||
| chr1:15412990 | C | T | 1 | a0001c0001t0001g0217 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.308+2711C>T | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15412990 | |||||||
| chr1:15412991 | G | A | 1 | a0001c0001t0001g0098 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.308+2712G>A | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15412991 | |||||||
| chr1:15413050 | C | T | 3 | a0001c0001t0007g0094 a0001c0001t0007g0095 a0001c0001t0016g0068 |
3 | HG01167.hp2 HG02922.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.308+2771C>T | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15413050 | |||||||
| chr1:15413112 | C | T | 5 | a0001c0001t0001g0042 a0001c0001t0001g0229 a0001c0001t0001g0230 others(2): Show |
6 | HG02630.hp2 HG02723.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.308+2833C>T | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15413112 | |||||||
| chr1:15413201 | A | C | 111 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0009 others(108): Show |
151 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.308+2922A>C | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15413201 | |||||||
| chr1:15413211 | G | C | 1 | a0001c0001t0001g0222 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.308+2932G>C | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15413211 | |||||||
| chr1:15413265 | A | G | 1 | a0001c0001t0001g0216 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.308+2986A>G | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15413265 | |||||||
| chr1:15413505 | G | A | 14 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0056 others(11): Show |
14 | HG01099.hp2 HG01346.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.308+3226G>A | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15413505 | |||||||
| chr1:15413634 | C | G | 1 | a0001c0001t0001g0093 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.308+3355C>G | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15413634 | |||||||
| chr1:15413795 | C | T | 18 | a0001c0001t0001g0022 a0001c0001t0001g0043 a0001c0001t0001g0045 others(15): Show |
23 | HG01070.hp1 HG01071.hp1 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.308+3516C>T | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15413795 | |||||||
| chr1:15413888 | G | A | 6 | a0001c0001t0001g0288 a0001c0001t0001g0291 a0001c0001t0001g0292 others(3): Show |
6 | HG01070.hp2 HG01099.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.308+3609G>A | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15413888 | |||||||
| chr1:15413894 | G | A | 1 | a0001c0001t0001g0121 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.308+3615G>A | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15413894 | |||||||
| chr1:15413933 | G | A | 2 | a0001c0001t0001g0123 a0001c0001t0003g0122 |
2 | HG03490.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.308+3654G>A | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15413933 | |||||||
| chr1:15414020 | G | A | 9 | a0001c0001t0001g0026 a0001c0001t0001g0098 a0001c0001t0001g0099 others(6): Show |
10 | HG02258.hp1 HG02818.hp1 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.308+3741G>A | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15414020 | |||||||
| chr1:15414231 | C | T | 1 | a0001c0001t0001g0069 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.308+3952C>T | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15414231 | |||||||
| chr1:15414434 | C | T | 30 | a0001c0001t0001g0015 a0001c0001t0001g0265 a0001c0001t0001g0268 others(27): Show |
43 | HG00438.hp1 HG00544.hp2 HG00558.hp1 others(40): Show |
intron_variant | MODIFIER | c.308+4155C>T | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15414434 | |||||||
| chr1:15414444 | C | T | 1 | a0001c0001t0001g0215 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.308+4165C>T | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15414444 | |||||||
| chr1:15414471 | C | T | 1 | a0001c0001t0001g0214 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.308+4192C>T | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15414471 | |||||||
| chr1:15414713 | C | T | 1 | a0001c0001t0002g0119 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.308+4434C>T | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15414713 | |||||||
| chr1:15414721 | A | G | 1 | a0001c0001t0001g0213 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.308+4442A>G | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15414721 | |||||||
| chr1:15414907 | C | T | 2 | a0001c0001t0002g0211 a0001c0001t0002g0212 |
2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.308+4628C>T | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15414907 | |||||||
| chr1:15414989 | C | G | 1 | a0001c0001t0001g0251 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.308+4710C>G | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15414989 | |||||||
| chr1:15415091 | G | T | 2 | a0001c0001t0001g0025 a0001c0001t0003g0025 |
2 | HG01255.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.308+4812G>T | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15415091 | |||||||
| chr1:15415109 | G | A | 1 | a0001c0001t0012g0232 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.308+4830G>A | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15415109 | |||||||
| chr1:15415220 | A | G | 3 | a0001c0001t0002g0238 a0001c0001t0002g0239 a0001c0001t0019g0240 |
3 | HG00642.hp2 HG01074.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.308+4941A>G | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15415220 | |||||||
| chr1:15415235 | G | A | 1 | a0001c0001t0025g0231 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.308+4956G>A | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15415235 | |||||||
| chr1:15415327 | A | G | 4 | a0001c0001t0001g0222 a0001c0001t0002g0238 a0001c0001t0002g0239 others(1): Show |
4 | HG00642.hp2 HG01074.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.308+5048A>G | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15415327 | |||||||
| chr1:15415364 | G | A | 50 | a0001c0001t0001g0015 a0001c0001t0001g0054 a0001c0001t0001g0055 others(47): Show |
64 | HG00438.hp1 HG00544.hp2 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.308+5085G>A | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15415364 | |||||||
| chr1:15415423 | A | G | 1 | a0001c0001t0002g0237 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.308+5144A>G | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15415423 | |||||||
| chr1:15415490 | C | CT | 32 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0018 others(29): Show |
48 | HG00323.hp2 HG00423.hp1 HG00673.hp1 others(45): Show |
intron_variant | MODIFIER | c.308+5227dupT | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 15415490 | ||||||
| chr1:15415596 | C | T | 1 | a0001c0001t0001g0066 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.308+5317C>T | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15415596 | |||||||
| chr1:15415770 | G | A | 3 | a0001c0001t0001g0125 a0001c0001t0003g0126 a0001c0001t0022g0124 |
3 | NA18941.hp2 NA18953.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.308+5491G>A | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15415770 | |||||||
| chr1:15415795 | C | T | 9 | a0001c0001t0001g0026 a0001c0001t0001g0098 a0001c0001t0001g0099 others(6): Show |
10 | HG02258.hp1 HG02818.hp1 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.308+5516C>T | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15415795 | |||||||
| chr1:15415804 | T | A | 1 | a0001c0001t0015g0264 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.308+5525T>A | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15415804 | |||||||
| chr1:15415925 | A | AAGTGAAG others(4): Show |
1 | a0001c0001t0001g0120 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.308+5647_308+5657d others(13): Show |
EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 15415925 | ||||||
| chr1:15415954 | G | T | 1 | a0001c0001t0001g0286 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.308+5675G>T | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15415954 | |||||||
| chr1:15415956 | G | A | 2 | a0001c0001t0003g0304 a0001c0001t0003g0305 |
2 | HG01943.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.308+5677G>A | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15415956 | |||||||
| chr1:15416024 | T | G | 1 | a0001c0001t0002g0287 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.308+5745T>G | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15416024 | |||||||
| chr1:15416072 | G | T | 17 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0018 others(14): Show |
33 | HG00423.hp1 HG00621.hp1 HG00673.hp1 others(30): Show |
intron_variant | MODIFIER | c.308+5793G>T | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15416072 | |||||||
| chr1:15416082 | C | T | 2 | a0001c0001t0001g0096 a0001c0001t0001g0236 |
2 | HG03471.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.308+5803C>T | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15416082 | |||||||
| chr1:15416138 | C | G | 2 | a0001c0001t0015g0264 a0003c0004t0001g0295 |
2 | HG02922.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.308+5859C>G | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15416138 | |||||||
| chr1:15416193 | T | C | 118 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0015 others(115): Show |
145 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(142): Show |
intron_variant | MODIFIER | c.308+5914T>C | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15416193 | |||||||
| chr1:15416202 | C | G | 1 | a0001c0001t0002g0119 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.308+5923C>G | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15416202 | |||||||
| chr1:15416227 | G | C | 1 | a0001c0001t0003g0059 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.308+5948G>C | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15416227 | |||||||
| chr1:15416311 | G | C | 133 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0009 others(130): Show |
175 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(172): Show |
intron_variant | MODIFIER | c.308+6032G>C | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15416311 | |||||||
| chr1:15416333 | C | T | 3 | a0001c0001t0007g0094 a0001c0001t0007g0095 a0001c0001t0016g0068 |
3 | HG01167.hp2 HG02922.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.308+6054C>T | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15416333 | |||||||
| chr1:15416482 | T | A | 1 | a0001c0001t0001g0073 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.308+6203T>A | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15416482 | |||||||
| chr1:15416485 | G | A | 1 | a0001c0001t0001g0073 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.308+6206G>A | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15416485 | |||||||
| chr1:15416505 | G | A | 1 | a0001c0001t0001g0069 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.308+6226G>A | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15416505 | |||||||
| chr1:15416580 | C | A | 1 | a0001c0001t0002g0128 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.308+6301C>A | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15416580 | |||||||
| chr1:15416621 | C | G | 1 | a0001c0001t0001g0222 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.308+6342C>G | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15416621 | |||||||
| chr1:15416622 | A | G | 59 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0017 others(56): Show |
72 | HG00423.hp2 HG00438.hp2 HG01070.hp2 others(69): Show |
intron_variant | MODIFIER | c.308+6343A>G | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15416622 | |||||||
| chr1:15416752 | G | A | 2 | a0001c0001t0001g0069 a0003c0004t0001g0295 |
2 | HG02922.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.308+6473G>A | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15416752 | |||||||
| chr1:15416897 | C | T | 1 | a0001c0001t0001g0206 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.308+6618C>T | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15416897 | |||||||
| chr1:15417197 | G | A | 5 | a0001c0001t0001g0042 a0001c0001t0001g0229 a0001c0001t0001g0230 others(2): Show |
6 | HG02630.hp2 HG02723.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.308+6918G>A | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15417197 | |||||||
| chr1:15417313 | G | C | 1 | a0001c0001t0002g0028 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.308+7034G>C | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15417313 | |||||||
| chr1:15417329 | G | T | 2 | a0001c0001t0005g0220 a0001c0001t0005g0221 |
2 | HG02965.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.308+7050G>T | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15417329 | |||||||
| chr1:15417388 | A | C | 114 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0015 others(111): Show |
140 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(137): Show |
intron_variant | MODIFIER | c.308+7109A>C | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15417388 | |||||||
| chr1:15417492 | T | C | 1 | a0001c0001t0001g0070 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.308+7213T>C | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15417492 | |||||||
| chr1:15417508 | T | C | 3 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0129 |
5 | HG00140.hp2 HG01358.hp2 HG01934.hp1 others(2): Show |
intron_variant | MODIFIER | c.308+7229T>C | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15417508 | |||||||
| chr1:15417515 | C | G | 32 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0017 others(29): Show |
42 | HG00423.hp2 HG00438.hp2 HG00733.hp2 others(39): Show |
intron_variant | MODIFIER | c.308+7236C>G | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15417515 | |||||||
| chr1:15417521 | G | A | 1 | a0001c0001t0002g0238 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.308+7242G>A | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15417521 | |||||||
| chr1:15417561 | G | T | 55 | a0001c0001t0001g0015 a0001c0001t0001g0054 a0001c0001t0001g0055 others(52): Show |
69 | HG00438.hp1 HG00544.hp2 HG00558.hp1 others(66): Show |
intron_variant | MODIFIER | c.308+7282G>T | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15417561 | |||||||
| chr1:15417599 | C | T | 1 | a0001c0001t0020g0205 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.308+7320C>T | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15417599 | |||||||
| chr1:15417667 | C | T | 1 | a0001c0001t0001g0204 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.308+7388C>T | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15417667 | |||||||
| chr1:15417678 | C | T | 1 | a0001c0001t0001g0203 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.308+7399C>T | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15417678 | |||||||
| chr1:15417775 | T | C | 83 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0051 others(80): Show |
99 | HG00438.hp1 HG00544.hp2 HG00558.hp1 others(96): Show |
intron_variant | MODIFIER | c.308+7496T>C | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15417775 | |||||||
| chr1:15417791 | C | T | 31 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0017 others(28): Show |
41 | HG00423.hp2 HG00438.hp2 HG00733.hp2 others(38): Show |
intron_variant | MODIFIER | c.308+7512C>T | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15417791 | |||||||
| chr1:15417802 | T | C | 1 | a0001c0001t0001g0265 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.308+7523T>C | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15417802 | |||||||
| chr1:15417884 | C | A | 13 | a0001c0001t0001g0042 a0001c0001t0001g0228 a0001c0001t0001g0229 others(10): Show |
14 | HG00735.hp2 HG00738.hp2 HG01069.hp2 others(11): Show |
intron_variant | MODIFIER | c.308+7605C>A | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15417884 | |||||||
| chr1:15417955 | C | G | 78 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0015 others(75): Show |
110 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(107): Show |
intron_variant | MODIFIER | c.308+7676C>G | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15417955 | |||||||
| chr1:15417958 | G | A | 2 | a0001c0001t0001g0069 a0001c0001t0015g0264 |
2 | HG03130.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.308+7679G>A | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15417958 | |||||||
| chr1:15417981 | C | CT | 16 | a0001c0001t0001g0192 a0001c0001t0001g0193 a0001c0001t0001g0195 others(13): Show |
16 | HG01175.hp1 HG01346.hp1 HG01928.hp2 others(13): Show |
intron_variant | MODIFIER | c.308+7728dupT | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 15417981 | ||||||
| chr1:15417981 | CT | C | 65 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0017 others(62): Show |
80 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(77): Show |
intron_variant | MODIFIER | c.308+7728delT | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 15417981 | ||||||
| chr1:15417981 | CTT | C | 6 | a0001c0001t0001g0076 a0001c0001t0001g0241 a0001c0001t0001g0242 others(3): Show |
6 | HG01070.hp1 HG02109.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.308+7727_308+7728d others(4): Show |
EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 15417981 | ||||||
| chr1:15417981 | CTTT | C | 10 | a0001c0001t0001g0026 a0001c0001t0001g0051 a0001c0001t0001g0098 others(7): Show |
12 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.308+7726_308+7728d others(5): Show |
EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 15417981 | ||||||
| chr1:15417981 | CTTTT | C | 15 | a0001c0001t0001g0099 a0001c0001t0001g0101 a0001c0001t0001g0233 others(12): Show |
15 | HG01070.hp2 HG01099.hp1 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.308+7725_308+7728d others(6): Show |
EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 15417981 | ||||||
| chr1:15417983 | T | TTTTC | 14 | a0001c0001t0001g0042 a0001c0001t0001g0069 a0001c0001t0001g0228 others(11): Show |
15 | HG00735.hp2 HG00738.hp2 HG01069.hp2 others(12): Show |
intron_variant | MODIFIER | c.308+7707_308+7708i others(6): Show |
EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 15417983 | ||||||
| chr1:15417984 | T | TTTC | 6 | a0001c0001t0001g0282 a0001c0001t0002g0024 a0001c0001t0002g0050 others(3): Show |
9 | NA18906.hp2 NA18951.hp1 NA18954.hp2 others(6): Show |
intron_variant | MODIFIER | c.308+7707_308+7708i others(5): Show |
EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 15417984 | ||||||
| chr1:15417985 | T | TTC | 55 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0018 others(52): Show |
75 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.308+7707_308+7708i others(4): Show |
EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 15417985 | ||||||
| chr1:15417986 | T | TC | 16 | a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0070 others(13): Show |
25 | HG01167.hp2 HG01496.hp2 HG01934.hp2 others(22): Show |
intron_variant | MODIFIER | c.308+7707_308+7708i others(3): Show |
EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15417986 | |||||||
| chr1:15417987 | T | C | 1 | a0001c0001t0003g0109 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.308+7708T>C | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15417987 | |||||||
| chr1:15417990 | T | C | 10 | a0001c0001t0001g0026 a0001c0001t0001g0051 a0001c0001t0001g0098 others(7): Show |
12 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.308+7711T>C | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15417990 | |||||||
| chr1:15417991 | T | C | 15 | a0001c0001t0001g0099 a0001c0001t0001g0101 a0001c0001t0001g0233 others(12): Show |
15 | HG01070.hp2 HG01099.hp1 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.308+7712T>C | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15417991 | |||||||
| chr1:15417992 | T | C | 1 | a0001c0001t0001g0104 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.308+7713T>C | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15417992 | |||||||
| chr1:15418044 | C | T | 1 | a0001c0001t0003g0305 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.308+7765C>T | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15418044 | |||||||
| chr1:15418110 | C | A | 25 | a0001c0001t0001g0026 a0001c0001t0001g0051 a0001c0001t0001g0098 others(22): Show |
27 | HG01070.hp2 HG01099.hp1 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.309-7761C>A | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15418110 | |||||||
| chr1:15418113 | C | T | 1 | a0001c0001t0003g0126 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.309-7758C>T | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15418113 | |||||||
| chr1:15418181 | G | A | 30 | a0001c0001t0001g0015 a0001c0001t0001g0265 a0001c0001t0001g0268 others(27): Show |
43 | HG00438.hp1 HG00544.hp2 HG00558.hp1 others(40): Show |
intron_variant | MODIFIER | c.309-7690G>A | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15418181 | |||||||
| chr1:15418228 | G | A | 2 | a0001c0001t0001g0268 a0001c0001t0002g0269 |
2 | HG01074.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.309-7643G>A | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15418228 | |||||||
| chr1:15418237 | G | A | 1 | a0001c0001t0001g0069 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.309-7634G>A | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15418237 | |||||||
| chr1:15418269 | C | T | 13 | a0001c0001t0001g0042 a0001c0001t0001g0228 a0001c0001t0001g0229 others(10): Show |
14 | HG00735.hp2 HG00738.hp2 HG01069.hp2 others(11): Show |
intron_variant | MODIFIER | c.309-7602C>T | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15418269 | |||||||
| chr1:15418290 | G | A | 13 | a0001c0001t0001g0042 a0001c0001t0001g0228 a0001c0001t0001g0229 others(10): Show |
14 | HG00735.hp2 HG00738.hp2 HG01069.hp2 others(11): Show |
intron_variant | MODIFIER | c.309-7581G>A | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15418290 | |||||||
| chr1:15418299 | C | CT | 20 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0127 others(17): Show |
20 | HG00621.hp2 HG01175.hp2 HG01516.hp2 others(17): Show |
intron_variant | MODIFIER | c.309-7548dupT | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 15418299 | ||||||
| chr1:15418299 | CT | C | 10 | a0001c0001t0001g0077 a0001c0001t0001g0141 a0001c0001t0001g0142 others(7): Show |
10 | HG02055.hp1 HG02896.hp1 HG03834.hp2 others(7): Show |
intron_variant | MODIFIER | c.309-7548delT | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 15418299 | ||||||
| chr1:15418299 | CTT | C | 83 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0018 others(80): Show |
105 | HG00423.hp1 HG00621.hp1 HG00673.hp1 others(102): Show |
intron_variant | MODIFIER | c.309-7549_309-7548d others(4): Show |
EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 15418299 | ||||||
| chr1:15418321 | T | C | 1 | a0001c0001t0001g0139 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.309-7550T>C | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15418321 | |||||||
| chr1:15418345 | A | G | 7 | a0001c0001t0001g0288 a0001c0001t0001g0291 a0001c0001t0001g0292 others(4): Show |
7 | HG01070.hp2 HG01099.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.309-7526A>G | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15418345 | |||||||
| chr1:15418366 | C | T | 6 | a0001c0001t0001g0051 a0001c0001t0002g0300 a0001c0001t0005g0051 others(3): Show |
7 | HG01243.hp2 HG01884.hp2 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.309-7505C>T | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15418366 | |||||||
| chr1:15418375 | G | A | 6 | a0001c0001t0001g0051 a0001c0001t0002g0300 a0001c0001t0005g0051 others(3): Show |
7 | HG01243.hp2 HG01884.hp2 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.309-7496G>A | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15418375 | |||||||
| chr1:15418392 | G | A | 6 | a0001c0001t0001g0051 a0001c0001t0002g0300 a0001c0001t0005g0051 others(3): Show |
7 | HG01243.hp2 HG01884.hp2 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.309-7479G>A | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15418392 | |||||||
| chr1:15418406 | C | T | 6 | a0001c0001t0001g0051 a0001c0001t0002g0300 a0001c0001t0005g0051 others(3): Show |
7 | HG01243.hp2 HG01884.hp2 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.309-7465C>T | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15418406 | |||||||
| chr1:15418414 | T | G | 6 | a0001c0001t0001g0051 a0001c0001t0002g0300 a0001c0001t0005g0051 others(3): Show |
7 | HG01243.hp2 HG01884.hp2 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.309-7457T>G | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15418414 | |||||||
| chr1:15418443 | C | T | 1 | a0001c0002t0007g0117 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.309-7428C>T | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15418443 | |||||||
| chr1:15418450 | C | G | 1 | a0001c0001t0001g0070 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.309-7421C>G | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15418450 | |||||||
| chr1:15418451 | G | T | 1 | a0001c0001t0001g0265 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.309-7420G>T | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15418451 | |||||||
| chr1:15418455 | A | G | 40 | a0001c0001t0001g0015 a0001c0001t0001g0042 a0001c0001t0001g0228 others(37): Show |
54 | HG00438.hp1 HG00544.hp2 HG00735.hp2 others(51): Show |
intron_variant | MODIFIER | c.309-7416A>G | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15418455 | |||||||
| chr1:15418459 | T | C | 2 | a0001c0001t0001g0070 a0001c0001t0002g0143 |
2 | HG02486.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.309-7412T>C | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15418459 | |||||||
| chr1:15418462 | C | T | 1 | a0001c0001t0002g0143 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.309-7409C>T | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15418462 | |||||||
| chr1:15418467 | G | A | 2 | a0001c0001t0001g0096 a0001c0001t0001g0236 |
2 | HG03471.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.309-7404G>A | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15418467 | |||||||
| chr1:15418495 | C | T | 1 | a0001c0001t0001g0104 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.309-7376C>T | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15418495 | |||||||
| chr1:15418496 | G | A | 8 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0078 others(5): Show |
10 | HG01081.hp1 HG01109.hp2 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.309-7375G>A | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15418496 | |||||||
| chr1:15418506 | C | T | 1 | a0001c0001t0002g0065 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.309-7365C>T | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15418506 | |||||||
| chr1:15418507 | G | A | 8 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0296 others(5): Show |
9 | HG00741.hp2 HG01515.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.309-7364G>A | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15418507 | |||||||
| chr1:15418508 | T | C | 1 | a0001c0001t0003g0144 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.309-7363T>C | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15418508 | |||||||
| chr1:15418511 | T | C | 8 | a0001c0001t0002g0065 a0001c0001t0003g0223 a0001c0001t0005g0220 others(5): Show |
8 | HG00735.hp2 HG00738.hp2 HG01069.hp2 others(5): Show |
intron_variant | MODIFIER | c.309-7360T>C | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15418511 | |||||||
| chr1:15418512 | A | G | 1 | a0001c0001t0003g0144 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.309-7359A>G | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15418512 | |||||||
| chr1:15418517 | G | A | 8 | a0001c0001t0001g0253 a0001c0001t0001g0256 a0001c0001t0002g0239 others(5): Show |
8 | HG00642.hp2 HG02109.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.309-7354G>A | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15418517 | |||||||
| chr1:15418519 | A | G | 7 | a0001c0001t0001g0051 a0001c0001t0002g0300 a0001c0001t0005g0051 others(4): Show |
8 | HG01243.hp2 HG01884.hp2 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.309-7352A>G | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15418519 | |||||||
| chr1:15418527 | A | C | 17 | a0001c0001t0001g0038 a0001c0001t0001g0051 a0001c0001t0001g0074 others(14): Show |
20 | HG01243.hp2 HG01884.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.309-7344A>C | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15418527 | |||||||
| chr1:15418527 | A | G | 41 | a0001c0001t0001g0042 a0001c0001t0001g0138 a0001c0001t0001g0180 others(38): Show |
43 | HG00280.hp2 HG00639.hp2 HG00642.hp2 others(40): Show |
intron_variant | MODIFIER | c.309-7344A>G | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15418527 | |||||||
| chr1:15418527 | A | T | 2 | a0001c0001t0001g0077 a0001c0001t0001g0087 |
2 | HG00438.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.309-7344A>T | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15418527 | |||||||
| chr1:15418540 | T | C | 67 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0017 others(64): Show |
83 | HG00423.hp2 HG00438.hp2 HG00642.hp2 others(80): Show |
intron_variant | MODIFIER | c.309-7331T>C | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15418540 | |||||||
| chr1:15418548 | G | A | 1 | a0001c0001t0003g0148 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.309-7323G>A | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15418548 | |||||||
| chr1:15418556 | T | C | 4 | a0001c0001t0001g0233 a0001c0001t0002g0293 a0001c0001t0003g0278 others(1): Show |
4 | HG02451.hp2 HG06807.hp2 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.309-7315T>C | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15418556 | |||||||
| chr1:15418562 | C | T | 1 | a0001c0001t0003g0278 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.309-7309C>T | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15418562 | |||||||
| chr1:15418582 | G | A | 205 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(202): Show |
262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.309-7289G>A | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15418582 | |||||||
| chr1:15418586 | G | T | 212 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(209): Show |
270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.309-7285G>T | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15418586 | |||||||
| chr1:15418593 | C | T | 1 | a0001c0001t0001g0176 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.309-7278C>T | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15418593 | |||||||
| chr1:15418594 | G | C | 109 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(106): Show |
148 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(145): Show |
intron_variant | MODIFIER | c.309-7277G>C | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15418594 | |||||||
| chr1:15418594 | G | T | 1 | a0001c0002t0007g0058 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.309-7277G>T | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15418594 | |||||||
| chr1:15418597 | A | C | 1 | a0001c0001t0001g0127 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.309-7274A>C | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15418597 | |||||||
| chr1:15418597 | A | G | 3 | a0001c0001t0001g0168 a0001c0001t0002g0140 a0001c0001t0002g0150 |
3 | HG03017.hp1 NA18941.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.309-7274A>G | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15418597 | |||||||
| chr1:15418597 | A | T | 106 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(103): Show |
145 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(142): Show |
intron_variant | MODIFIER | c.309-7274A>T | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15418597 | |||||||
| chr1:15418604 | C | T | 7 | a0001c0001t0001g0051 a0001c0001t0002g0300 a0001c0001t0005g0051 others(4): Show |
8 | HG01243.hp2 HG01884.hp2 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.309-7267C>T | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15418604 | |||||||
| chr1:15418636 | G | GGCC | 153 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(150): Show |
197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.309-7234_309-7232d others(5): Show |
EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 15418636 | ||||||
| chr1:15418728 | C | T | 2 | a0001c0001t0001g0188 a0001c0001t0002g0028 |
3 | HG01257.hp1 HG01258.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.309-7143C>T | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15418728 | |||||||
| chr1:15418729 | G | A | 1 | a0001c0001t0003g0109 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.309-7142G>A | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15418729 | |||||||
| chr1:15418758 | C | T | 190 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0009 others(187): Show |
241 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(238): Show |
intron_variant | MODIFIER | c.309-7113C>T | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15418758 | |||||||
| chr1:15418786 | T | C | 169 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0009 others(166): Show |
219 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(216): Show |
intron_variant | MODIFIER | c.309-7085T>C | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15418786 | |||||||
| chr1:15418848 | GAGCCC | G | 99 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0015 others(96): Show |
129 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(126): Show |
intron_variant | MODIFIER | c.309-7019_309-7015d others(7): Show |
EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 15418848 | ||||||
| chr1:15418856 | C | T | 2 | a0001c0001t0018g0118 a0001c0001t0019g0240 |
2 | HG00642.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.309-7015C>T | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15418856 | |||||||
| chr1:15418884 | T | C | 139 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0009 others(136): Show |
187 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(184): Show |
intron_variant | MODIFIER | c.309-6987T>C | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15418884 | |||||||
| chr1:15418897 | C | T | 1 | a0001c0001t0006g0165 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.309-6974C>T | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15418897 | |||||||
| chr1:15418903 | G | A | 1 | a0001c0001t0002g0119 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.309-6968G>A | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15418903 | |||||||
| chr1:15419006 | A | G | 5 | a0001c0001t0001g0096 a0001c0001t0001g0236 a0001c0001t0009g0116 others(2): Show |
5 | HG01106.hp2 HG02572.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.309-6865A>G | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15419006 | |||||||
| chr1:15419171 | G | A | 1 | a0001c0001t0019g0240 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.309-6700G>A | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15419171 | |||||||
| chr1:15419182 | C | G | 11 | a0001c0001t0001g0042 a0001c0001t0001g0229 a0001c0001t0001g0230 others(8): Show |
12 | HG00735.hp2 HG00738.hp2 HG01069.hp2 others(9): Show |
intron_variant | MODIFIER | c.309-6689C>G | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15419182 | |||||||
| chr1:15419200 | G | A | 2 | a0001c0001t0001g0043 a0001c0001t0001g0242 |
3 | HG01070.hp1 HG01071.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.309-6671G>A | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15419200 | |||||||
| chr1:15419232 | G | A | 6 | a0001c0001t0001g0130 a0001c0001t0001g0152 a0001c0001t0002g0049 others(3): Show |
7 | HG01109.hp1 HG01255.hp2 HG01261.hp1 others(4): Show |
intron_variant | MODIFIER | c.309-6639G>A | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15419232 | |||||||
| chr1:15419276 | A | G | 20 | a0001c0001t0001g0022 a0001c0001t0001g0042 a0001c0001t0001g0043 others(17): Show |
25 | HG01070.hp1 HG01071.hp1 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.309-6595A>G | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15419276 | |||||||
| chr1:15419291 | C | A | 14 | a0001c0001t0001g0026 a0001c0001t0001g0054 a0001c0001t0001g0055 others(11): Show |
15 | HG02055.hp2 HG02109.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.309-6580C>A | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15419291 | |||||||
| chr1:15419365 | C | T | 4 | a0001c0001t0001g0037 a0001c0001t0001g0164 a0001c0001t0001g0168 others(1): Show |
5 | HG02698.hp1 HG02735.hp1 HG03017.hp1 others(2): Show |
intron_variant | MODIFIER | c.309-6506C>T | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15419365 | |||||||
| chr1:15419451 | A | G | 1 | a0001c0001t0001g0090 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.309-6420A>G | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15419451 | |||||||
| chr1:15419530 | A | AG | 106 | a0001c0001t0001g0014 a0001c0001t0001g0017 a0001c0001t0001g0026 others(103): Show |
118 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.309-6337dupG | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 15419530 | ||||||
| chr1:15419573 | A | C | 45 | a0001c0001t0001g0026 a0001c0001t0001g0043 a0001c0001t0001g0045 others(42): Show |
51 | HG00639.hp2 HG01069.hp2 HG01070.hp1 others(48): Show |
intron_variant | MODIFIER | c.309-6298A>C | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15419573 | |||||||
| chr1:15419582 | G | C | 1 | a0001c0001t0002g0290 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.309-6289G>C | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15419582 | |||||||
| chr1:15419665 | G | C | 15 | a0001c0001t0001g0026 a0001c0001t0001g0042 a0001c0001t0001g0045 others(12): Show |
17 | HG02055.hp2 HG02258.hp2 HG02630.hp2 others(14): Show |
intron_variant | MODIFIER | c.309-6206G>C | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15419665 | |||||||
| chr1:15419749 | T | C | 57 | a0001c0001t0001g0026 a0001c0001t0001g0042 a0001c0001t0001g0043 others(54): Show |
63 | HG00099.hp2 HG01070.hp1 HG01071.hp1 others(60): Show |
intron_variant | MODIFIER | c.309-6122T>C | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15419749 | |||||||
| chr1:15419923 | T | C | 1 | a0001c0001t0003g0179 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.309-5948T>C | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15419923 | |||||||
| chr1:15419958 | C | T | 1 | a0001c0001t0025g0231 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.309-5913C>T | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15419958 | |||||||
| chr1:15420027 | T | C | 1 | a0001c0001t0002g0273 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.309-5844T>C | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15420027 | |||||||
| chr1:15420085 | C | T | 1 | a0001c0001t0001g0096 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.309-5786C>T | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15420085 | |||||||
| chr1:15420087 | C | T | 5 | a0001c0001t0001g0043 a0001c0001t0001g0096 a0001c0001t0001g0236 others(2): Show |
6 | HG01070.hp1 HG01071.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.309-5784C>T | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15420087 | |||||||
| chr1:15420109 | T | C | 1 | a0001c0001t0001g0265 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.309-5762T>C | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15420109 | |||||||
| chr1:15420160 | A | T | 27 | a0001c0001t0001g0042 a0001c0001t0001g0045 a0001c0001t0001g0123 others(24): Show |
30 | HG01069.hp2 HG01071.hp2 HG01074.hp2 others(27): Show |
intron_variant | MODIFIER | c.309-5711A>T | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15420160 | |||||||
| chr1:15420241 | A | G | 7 | a0001c0001t0005g0220 a0001c0001t0005g0221 a0001c0001t0007g0094 others(4): Show |
7 | HG01106.hp2 HG01109.hp2 HG01167.hp2 others(4): Show |
intron_variant | MODIFIER | c.309-5630A>G | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15420241 | |||||||
| chr1:15420242 | T | C | 5 | a0001c0001t0005g0220 a0001c0001t0005g0221 a0001c0001t0009g0116 others(2): Show |
5 | HG01106.hp2 HG01109.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.309-5629T>C | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15420242 | |||||||
| chr1:15420252 | A | G | 5 | a0001c0001t0001g0243 a0001c0001t0001g0248 a0001c0001t0001g0261 others(2): Show |
5 | HG02145.hp2 HG02717.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.309-5619A>G | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15420252 | |||||||
| chr1:15420297 | T | C | 67 | a0001c0001t0001g0022 a0001c0001t0001g0042 a0001c0001t0001g0043 others(64): Show |
78 | HG00639.hp1 HG01069.hp2 HG01070.hp1 others(75): Show |
intron_variant | MODIFIER | c.309-5574T>C | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15420297 | |||||||
| chr1:15420508 | A | ATTAT | 4 | a0001c0001t0001g0026 a0001c0001t0001g0054 a0001c0001t0001g0055 others(1): Show |
5 | HG02055.hp2 HG02258.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.309-5340_309-5337d others(6): Show |
EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 15420508 | ||||||
| chr1:15420508 | A | ATTATTTA others(5): Show |
3 | a0001c0002t0010g0225 a0001c0002t0010g0226 a0001c0002t0010g0227 |
3 | HG01069.hp2 HG01071.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.309-5348_309-5337d others(14): Show |
EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 15420508 | ||||||
| chr1:15420508 | A | ATTATTTA others(9): Show |
9 | a0001c0002t0001g0044 a0001c0002t0001g0057 a0001c0002t0001g0061 others(6): Show |
10 | HG01891.hp1 HG02055.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.309-5352_309-5337d others(18): Show |
EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 15420508 | ||||||
| chr1:15420508 | A | ATTATTTA others(13): Show |
4 | a0001c0002t0007g0063 a0001c0002t0007g0117 a0001c0002t0009g0034 others(1): Show |
5 | HG01257.hp2 HG02280.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.309-5356_309-5337d others(22): Show |
EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 15420508 | ||||||
| chr1:15420606 | A | G | 18 | a0001c0001t0001g0042 a0001c0001t0002g0042 a0001c0002t0001g0044 others(15): Show |
20 | HG01069.hp2 HG01071.hp2 HG01257.hp2 others(17): Show |
intron_variant | MODIFIER | c.309-5265A>G | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15420606 | |||||||
| chr1:15420618 | C | T | 1 | a0001c0001t0001g0074 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.309-5253C>T | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15420618 | |||||||
| chr1:15420739 | C | T | 17 | a0001c0001t0001g0042 a0001c0001t0002g0042 a0001c0002t0001g0044 others(14): Show |
18 | HG01069.hp2 HG01071.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.309-5132C>T | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15420739 | |||||||
| chr1:15421335 | C | T | 7 | a0001c0001t0001g0051 a0001c0001t0001g0123 a0001c0001t0002g0238 others(4): Show |
8 | HG01074.hp2 HG01243.hp2 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.309-4536C>T | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15421335 | |||||||
| chr1:15421351 | TG | T | 7 | a0001c0001t0001g0042 a0001c0001t0002g0042 a0001c0002t0009g0034 others(4): Show |
8 | HG01069.hp2 HG01071.hp2 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.309-4517delG | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 15421351 | ||||||
| chr1:15421391 | C | T | 4 | a0001c0001t0001g0045 a0001c0001t0001g0130 a0001c0001t0001g0152 others(1): Show |
5 | HG02895.hp1 HG02897.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.309-4480C>T | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15421391 | |||||||
| chr1:15421415 | C | T | 11 | a0001c0002t0001g0044 a0001c0002t0001g0057 a0001c0002t0001g0061 others(8): Show |
12 | HG01891.hp1 HG02055.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.309-4456C>T | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15421415 | |||||||
| chr1:15421458 | C | G | 1 | a0001c0001t0001g0159 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.309-4413C>G | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15421458 | |||||||
| chr1:15421598 | G | A | 4 | a0001c0001t0001g0056 a0001c0001t0001g0230 a0001c0001t0001g0249 others(1): Show |
4 | HG01515.hp2 HG03209.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.309-4273G>A | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15421598 | |||||||
| chr1:15421706 | C | A | 7 | a0001c0001t0001g0042 a0001c0001t0002g0042 a0001c0002t0009g0034 others(4): Show |
8 | HG01069.hp2 HG01071.hp2 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.309-4165C>A | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15421706 | |||||||
| chr1:15421863 | T | C | 18 | a0001c0001t0001g0042 a0001c0001t0002g0042 a0001c0002t0001g0044 others(15): Show |
20 | HG01069.hp2 HG01071.hp2 HG01257.hp2 others(17): Show |
intron_variant | MODIFIER | c.309-4008T>C | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15421863 | |||||||
| chr1:15421899 | C | A | 5 | a0001c0001t0008g0046 a0001c0001t0008g0246 a0001c0001t0008g0255 others(2): Show |
6 | HG02615.hp1 HG02896.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.309-3972C>A | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15421899 | |||||||
| chr1:15421938 | T | C | 6 | a0001c0001t0001g0042 a0001c0001t0002g0042 a0001c0002t0010g0225 others(3): Show |
6 | HG01069.hp2 HG01071.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.309-3933T>C | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15421938 | |||||||
| chr1:15422073 | C | CCAGGTCA others(2): Show |
3 | a0001c0001t0001g0076 a0001c0001t0001g0206 a0001c0001t0001g0209 |
3 | HG02135.hp2 NA18612.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.309-3796_309-3788d others(11): Show |
EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 15422073 | ||||||
| chr1:15422076 | G | C | 1 | a0001c0001t0001g0104 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.309-3795G>C | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15422076 | |||||||
| chr1:15422084 | C | CT | 3 | a0001c0001t0001g0026 a0001c0001t0001g0055 a0001c0001t0001g0103 |
4 | HG02258.hp2 HG02965.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.309-3787_309-3786i others(3): Show |
EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15422084 | |||||||
| chr1:15422085 | A | AT | 99 | a0001c0001t0001g0014 a0001c0001t0001g0025 a0001c0001t0001g0070 others(96): Show |
124 | HG00280.hp1 HG00280.hp2 HG00597.hp2 others(121): Show |
intron_variant | MODIFIER | c.309-3761dupT | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 15422085 | ||||||
| chr1:15422085 | A | ATT | 14 | a0001c0001t0001g0120 a0001c0001t0002g0050 a0001c0001t0002g0062 others(11): Show |
16 | HG00423.hp1 HG00621.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.309-3762_309-3761d others(4): Show |
EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 15422085 | ||||||
| chr1:15422085 | A | T | 4 | a0001c0001t0001g0026 a0001c0001t0001g0054 a0001c0001t0001g0055 others(1): Show |
5 | HG02055.hp2 HG02258.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.309-3786A>T | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15422085 | |||||||
| chr1:15422085 | AT | A | 22 | a0001c0001t0001g0042 a0001c0001t0001g0121 a0001c0001t0001g0131 others(19): Show |
25 | HG01071.hp2 HG01257.hp2 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.309-3761delT | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 15422085 | ||||||
| chr1:15422252 | C | G | 4 | a0001c0001t0001g0026 a0001c0001t0001g0054 a0001c0001t0001g0055 others(1): Show |
5 | HG02055.hp2 HG02258.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.309-3619C>G | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15422252 | |||||||
| chr1:15422430 | A | G | 18 | a0001c0001t0001g0042 a0001c0001t0002g0042 a0001c0002t0001g0044 others(15): Show |
20 | HG01069.hp2 HG01071.hp2 HG01257.hp2 others(17): Show |
intron_variant | MODIFIER | c.309-3441A>G | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15422430 | |||||||
| chr1:15422477 | C | T | 7 | a0001c0001t0001g0042 a0001c0001t0002g0042 a0001c0002t0009g0034 others(4): Show |
8 | HG01069.hp2 HG01071.hp2 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.309-3394C>T | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15422477 | |||||||
| chr1:15422485 | C | T | 2 | a0001c0001t0001g0130 a0001c0001t0001g0152 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.309-3386C>T | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15422485 | |||||||
| chr1:15422612 | A | G | 18 | a0001c0001t0001g0042 a0001c0001t0002g0042 a0001c0002t0001g0044 others(15): Show |
20 | HG01069.hp2 HG01071.hp2 HG01257.hp2 others(17): Show |
intron_variant | MODIFIER | c.309-3259A>G | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15422612 | |||||||
| chr1:15422719 | A | T | 7 | a0001c0001t0005g0220 a0001c0001t0005g0221 a0001c0001t0007g0094 others(4): Show |
7 | HG01106.hp2 HG01109.hp2 HG01167.hp2 others(4): Show |
intron_variant | MODIFIER | c.309-3152A>T | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15422719 | |||||||
| chr1:15422722 | G | A | 1 | a0001c0001t0001g0192 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.309-3149G>A | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15422722 | |||||||
| chr1:15422732 | G | T | 1 | a0001c0001t0001g0176 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.309-3139G>T | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15422732 | |||||||
| chr1:15422744 | G | C | 9 | a0001c0001t0001g0026 a0001c0001t0001g0054 a0001c0001t0001g0055 others(6): Show |
10 | HG02055.hp2 HG02145.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.309-3127G>C | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15422744 | |||||||
| chr1:15422786 | A | G | 39 | a0001c0001t0001g0026 a0001c0001t0001g0042 a0001c0001t0001g0051 others(36): Show |
44 | HG01069.hp2 HG01071.hp2 HG01074.hp2 others(41): Show |
intron_variant | MODIFIER | c.309-3085A>G | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15422786 | |||||||
| chr1:15422810 | A | G | 23 | a0001c0001t0001g0042 a0001c0001t0002g0042 a0001c0001t0008g0046 others(20): Show |
26 | HG01069.hp2 HG01071.hp2 HG01257.hp2 others(23): Show |
intron_variant | MODIFIER | c.309-3061A>G | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15422810 | |||||||
| chr1:15422947 | C | CCTT | 23 | a0001c0001t0001g0042 a0001c0001t0002g0042 a0001c0001t0008g0046 others(20): Show |
26 | HG01069.hp2 HG01071.hp2 HG01257.hp2 others(23): Show |
intron_variant | MODIFIER | c.309-2923_309-2921d others(5): Show |
EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 15422947 | ||||||
| chr1:15423068 | C | G | 21 | a0001c0001t0008g0046 a0001c0001t0008g0246 a0001c0001t0008g0255 others(18): Show |
24 | HG01069.hp2 HG01071.hp2 HG01257.hp2 others(21): Show |
intron_variant | MODIFIER | c.309-2803C>G | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15423068 | |||||||
| chr1:15423085 | C | T | 1 | a0001c0001t0001g0081 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.309-2786C>T | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15423085 | |||||||
| chr1:15423115 | G | A | 2 | a0001c0002t0007g0058 a0001c0002t0007g0100 |
2 | HG02145.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.309-2756G>A | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15423115 | |||||||
| chr1:15423314 | A | AG | 10 | a0001c0001t0008g0046 a0001c0001t0008g0246 a0001c0001t0008g0255 others(7): Show |
12 | HG01069.hp2 HG01071.hp2 HG01257.hp2 others(9): Show |
intron_variant | MODIFIER | c.309-2556dupG | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 15423314 | ||||||
| chr1:15423363 | T | C | 4 | a0001c0001t0001g0026 a0001c0001t0001g0054 a0001c0001t0001g0055 others(1): Show |
5 | HG02055.hp2 HG02258.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.309-2508T>C | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15423363 | |||||||
| chr1:15423616 | G | A | 6 | a0001c0002t0001g0044 a0001c0002t0001g0061 a0001c0002t0001g0064 others(3): Show |
7 | HG01891.hp1 HG02055.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.309-2255G>A | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15423616 | |||||||
| chr1:15423721 | A | G | 190 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0014 others(187): Show |
245 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(242): Show |
intron_variant | MODIFIER | c.309-2150A>G | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15423721 | |||||||
| chr1:15423782 | G | A | 16 | a0001c0001t0008g0046 a0001c0001t0008g0246 a0001c0001t0008g0255 others(13): Show |
18 | HG01891.hp1 HG02055.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.309-2089G>A | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15423782 | |||||||
| chr1:15423822 | C | T | 1 | a0001c0001t0008g0260 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.309-2049C>T | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15423822 | |||||||
| chr1:15423823 | G | A | 1 | a0001c0001t0005g0221 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.309-2048G>A | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15423823 | |||||||
| chr1:15423883 | C | T | 1 | a0001c0001t0001g0157 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.309-1988C>T | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15423883 | |||||||
| chr1:15423943 | A | G | 4 | a0001c0001t0001g0026 a0001c0001t0001g0054 a0001c0001t0001g0055 others(1): Show |
5 | HG02055.hp2 HG02258.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.309-1928A>G | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15423943 | |||||||
| chr1:15424047 | C | T | 1 | a0001c0001t0001g0054 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.309-1824C>T | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15424047 | |||||||
| chr1:15424060 | C | T | 3 | a0001c0001t0009g0116 a0001c0001t0009g0234 a0001c0001t0009g0299 |
3 | HG01106.hp2 HG01109.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.309-1811C>T | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15424060 | |||||||
| chr1:15424233 | C | A | 1 | a0001c0001t0001g0099 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.309-1638C>A | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15424233 | |||||||
| chr1:15424399 | G | T | 1 | a0001c0001t0003g0113 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.309-1472G>T | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15424399 | |||||||
| chr1:15424482 | G | A | 2 | a0001c0002t0007g0063 a0001c0002t0007g0117 |
2 | HG02280.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.309-1389G>A | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15424482 | |||||||
| chr1:15424606 | G | A | 4 | a0001c0001t0001g0056 a0001c0001t0001g0230 a0001c0001t0001g0249 others(1): Show |
4 | HG01515.hp2 HG03209.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.309-1265G>A | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15424606 | |||||||
| chr1:15424631 | C | T | 1 | a0003c0004t0001g0295 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.309-1240C>T | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15424631 | |||||||
| chr1:15424640 | T | C | 1 | a0001c0001t0002g0065 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.309-1231T>C | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15424640 | |||||||
| chr1:15424660 | G | A | 5 | a0001c0001t0001g0051 a0001c0001t0005g0051 a0001c0001t0005g0052 others(2): Show |
6 | HG01243.hp2 HG01891.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.309-1211G>A | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15424660 | |||||||
| chr1:15424678 | G | A | 1 | a0001c0001t0019g0240 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.309-1193G>A | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15424678 | |||||||
| chr1:15424685 | G | A | 11 | a0001c0002t0001g0044 a0001c0002t0001g0057 a0001c0002t0001g0061 others(8): Show |
12 | HG01891.hp1 HG02055.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.309-1186G>A | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15424685 | |||||||
| chr1:15424701 | A | G | 16 | a0001c0002t0001g0044 a0001c0002t0001g0057 a0001c0002t0001g0061 others(13): Show |
18 | HG01069.hp2 HG01071.hp2 HG01257.hp2 others(15): Show |
intron_variant | MODIFIER | c.309-1170A>G | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15424701 | |||||||
| chr1:15424747 | T | C | 1 | a0001c0001t0001g0123 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.309-1124T>C | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15424747 | |||||||
| chr1:15424776 | C | T | 2 | a0001c0001t0001g0262 a0001c0001t0001g0292 |
2 | HG02717.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.309-1095C>T | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15424776 | |||||||
| chr1:15424817 | C | A | 2 | a0001c0001t0001g0130 a0001c0001t0001g0152 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.309-1054C>A | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15424817 | |||||||
| chr1:15424949 | C | G | 1 | a0001c0001t0001g0098 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.309-922C>G | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15424949 | |||||||
| chr1:15425253 | G | A | 16 | a0001c0002t0001g0044 a0001c0002t0001g0057 a0001c0002t0001g0061 others(13): Show |
18 | HG01069.hp2 HG01071.hp2 HG01257.hp2 others(15): Show |
intron_variant | MODIFIER | c.309-618G>A | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15425253 | |||||||
| chr1:15425473 | C | A | 2 | a0001c0001t0001g0125 a0001c0001t0001g0132 |
2 | HG00597.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.309-398C>A | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15425473 | |||||||
| chr1:15425479 | T | C | 4 | a0001c0001t0002g0048 a0001c0001t0002g0083 a0001c0001t0002g0200 others(1): Show |
5 | NA18956.hp2 NA18991.hp2 NA19003.hp2 others(2): Show |
intron_variant | MODIFIER | c.309-392T>C | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15425479 | |||||||
| chr1:15425507 | G | A | 28 | a0001c0001t0001g0051 a0001c0001t0002g0163 a0001c0001t0002g0238 others(25): Show |
32 | HG01069.hp2 HG01071.hp2 HG01074.hp2 others(29): Show |
intron_variant | MODIFIER | c.309-364G>A | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15425507 | |||||||
| chr1:15425524 | C | CA | 10 | a0001c0001t0001g0026 a0001c0001t0001g0054 a0001c0001t0001g0055 others(7): Show |
11 | HG02055.hp2 HG02258.hp2 HG02965.hp1 others(8): Show |
intron_variant | MODIFIER | c.309-335dupA | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 15425524 | ||||||
| chr1:15425524 | CA | C | 16 | a0001c0002t0001g0044 a0001c0002t0001g0057 a0001c0002t0001g0061 others(13): Show |
18 | HG01069.hp2 HG01071.hp2 HG01257.hp2 others(15): Show |
intron_variant | MODIFIER | c.309-335delA | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr1 | 15425524 | ||||||
| chr1:15425792 | C | T | 3 | a0001c0001t0001g0288 a0001c0001t0001g0291 a0001c0001t0014g0289 |
3 | HG01099.hp1 HG02809.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.309-79C>T | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15425792 | |||||||
| chr1:15425819 | G | A | 1 | a0001c0002t0007g0100 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.309-52G>A | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 1/3 | chr1 | 15425819 | |||||||
| chr1:15426034 | A | G | 2 | a0001c0001t0002g0263 a0001c0001t0002g0293 |
2 | NA19030.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.456+16A>G | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 2/3 | chr1 | 15426034 | |||||||
| chr1:15426220 | C | T | 55 | a0001c0001t0001g0042 a0001c0001t0002g0008 a0001c0001t0002g0013 others(52): Show |
74 | HG00639.hp1 HG00642.hp1 HG00642.hp2 others(71): Show |
intron_variant | MODIFIER | c.456+202C>T | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 2/3 | chr1 | 15426220 | |||||||
| chr1:15426221 | G | A | 15 | a0001c0002t0001g0044 a0001c0002t0001g0057 a0001c0002t0001g0061 others(12): Show |
16 | HG01069.hp2 HG01071.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.456+203G>A | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 2/3 | chr1 | 15426221 | |||||||
| chr1:15426278 | G | A | 1 | a0001c0001t0001g0178 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.456+260G>A | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 2/3 | chr1 | 15426278 | |||||||
| chr1:15426308 | C | G | 1 | a0001c0002t0009g0034 | 2 | HG01257.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.456+290C>G | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 2/3 | chr1 | 15426308 | |||||||
| chr1:15426333 | C | T | 1 | a0001c0001t0008g0246 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.456+315C>T | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 2/3 | chr1 | 15426333 | |||||||
| chr1:15426472 | C | G | 16 | a0001c0001t0016g0068 a0001c0002t0001g0044 a0001c0002t0001g0057 others(13): Show |
18 | HG01069.hp2 HG01071.hp2 HG01257.hp2 others(15): Show |
intron_variant | MODIFIER | c.456+454C>G | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 2/3 | chr1 | 15426472 | |||||||
| chr1:15426644 | G | A | 11 | a0001c0002t0001g0044 a0001c0002t0001g0057 a0001c0002t0001g0061 others(8): Show |
12 | HG01891.hp1 HG02055.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.457-506G>A | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 2/3 | chr1 | 15426644 | |||||||
| chr1:15426738 | G | A | 5 | a0001c0001t0001g0051 a0001c0001t0002g0238 a0001c0001t0005g0051 others(2): Show |
6 | HG01074.hp2 HG01243.hp2 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.457-412G>A | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 2/3 | chr1 | 15426738 | |||||||
| chr1:15426852 | G | A | 1 | a0001c0001t0015g0264 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.457-298G>A | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 2/3 | chr1 | 15426852 | |||||||
| chr1:15426902 | T | G | 59 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0009 others(56): Show |
84 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.457-248T>G | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 2/3 | chr1 | 15426902 | |||||||
| chr1:15426911 | C | G | 1 | a0001c0001t0025g0231 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.457-239C>G | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 2/3 | chr1 | 15426911 | |||||||
| chr1:15427018 | G | A | 3 | a0001c0001t0002g0062 a0001c0001t0002g0300 a0001c0001t0019g0240 |
3 | HG00642.hp2 HG01884.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.457-132G>A | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 2/3 | chr1 | 15427018 | |||||||
| chr1:15427332 | C | A | 1 | a0001c0001t0001g0142 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.591+48C>A | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 3/3 | chr1 | 15427332 | |||||||
| chr1:15427432 | C | T | 1 | a0001c0001t0001g0070 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.591+148C>T | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 3/3 | chr1 | 15427432 | |||||||
| chr1:15427480 | C | T | 1 | a0001c0001t0001g0123 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.591+196C>T | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 3/3 | chr1 | 15427480 | |||||||
| chr1:15427487 | G | A | 1 | a0001c0001t0025g0231 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.591+203G>A | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 3/3 | chr1 | 15427487 | |||||||
| chr1:15427541 | G | A | 2 | a0001c0001t0001g0253 a0001c0001t0001g0256 |
2 | HG02257.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.591+257G>A | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 3/3 | chr1 | 15427541 | |||||||
| chr1:15427559 | A | T | 15 | a0001c0001t0016g0068 a0001c0002t0001g0044 a0001c0002t0001g0057 others(12): Show |
16 | HG01069.hp2 HG01071.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.591+275A>T | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 3/3 | chr1 | 15427559 | |||||||
| chr1:15427560 | G | C | 1 | a0001c0001t0001g0172 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.591+276G>C | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 3/3 | chr1 | 15427560 | |||||||
| chr1:15427594 | G | A | 2 | a0001c0001t0001g0127 a0001c0001t0001g0155 |
2 | NA19002.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.591+310G>A | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 3/3 | chr1 | 15427594 | |||||||
| chr1:15427676 | C | G | 20 | a0001c0001t0008g0046 a0001c0001t0008g0246 a0001c0001t0008g0255 others(17): Show |
22 | HG01069.hp2 HG01071.hp2 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.591+392C>G | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 3/3 | chr1 | 15427676 | |||||||
| chr1:15427701 | T | C | 20 | a0001c0001t0008g0046 a0001c0001t0008g0246 a0001c0001t0008g0255 others(17): Show |
22 | HG01069.hp2 HG01071.hp2 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.591+417T>C | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 3/3 | chr1 | 15427701 | |||||||
| chr1:15427743 | C | T | 5 | a0001c0001t0008g0046 a0001c0001t0008g0246 a0001c0001t0008g0255 others(2): Show |
6 | HG02615.hp1 HG02896.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.591+459C>T | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 3/3 | chr1 | 15427743 | |||||||
| chr1:15427759 | T | C | 1 | a0001c0001t0001g0154 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.591+475T>C | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 3/3 | chr1 | 15427759 | |||||||
| chr1:15427778 | G | A | 5 | a0001c0001t0001g0043 a0001c0001t0001g0096 a0001c0001t0001g0101 others(2): Show |
6 | HG01070.hp1 HG01071.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.591+494G>A | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 3/3 | chr1 | 15427778 | |||||||
| chr1:15427781 | G | A | 1 | a0001c0001t0002g0238 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.591+497G>A | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 3/3 | chr1 | 15427781 | |||||||
| chr1:15427872 | T | G | 1 | a0001c0001t0001g0096 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.591+588T>G | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 3/3 | chr1 | 15427872 | |||||||
| chr1:15427875 | T | C | 20 | a0001c0001t0008g0046 a0001c0001t0008g0246 a0001c0001t0008g0255 others(17): Show |
22 | HG01069.hp2 HG01071.hp2 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.591+591T>C | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 3/3 | chr1 | 15427875 | |||||||
| chr1:15427965 | G | A | 1 | a0001c0001t0001g0236 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.592-628G>A | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 3/3 | chr1 | 15427965 | |||||||
| chr1:15427988 | T | C | 302 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(299): Show |
397 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(394): Show |
intron_variant | MODIFIER | c.592-605T>C | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 3/3 | chr1 | 15427988 | |||||||
| chr1:15428017 | A | C | 16 | a0001c0001t0008g0046 a0001c0001t0008g0246 a0001c0001t0008g0255 others(13): Show |
18 | HG01891.hp1 HG02055.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.592-576A>C | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 3/3 | chr1 | 15428017 | |||||||
| chr1:15428030 | C | G | 1 | a0001c0001t0001g0250 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.592-563C>G | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 3/3 | chr1 | 15428030 | |||||||
| chr1:15428040 | C | A | 20 | a0001c0001t0008g0046 a0001c0001t0008g0246 a0001c0001t0008g0255 others(17): Show |
22 | HG01069.hp2 HG01071.hp2 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.592-553C>A | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 3/3 | chr1 | 15428040 | |||||||
| chr1:15428071 | A | C | 1 | a0001c0001t0001g0129 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.592-522A>C | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 3/3 | chr1 | 15428071 | |||||||
| chr1:15428214 | C | T | 6 | a0001c0001t0001g0022 a0001c0001t0001g0067 a0001c0001t0001g0241 others(3): Show |
8 | HG01884.hp1 HG02647.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.592-379C>T | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 3/3 | chr1 | 15428214 | |||||||
| chr1:15428353 | C | T | 3 | a0001c0001t0001g0274 a0001c0001t0001g0279 a0001c0001t0001g0282 |
3 | NA18939.hp2 NA18959.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.592-240C>T | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 3/3 | chr1 | 15428353 | |||||||
| chr1:15428370 | A | G | 26 | a0001c0001t0001g0026 a0001c0001t0001g0054 a0001c0001t0001g0055 others(23): Show |
29 | HG01069.hp2 HG01071.hp2 HG01074.hp2 others(26): Show |
intron_variant | MODIFIER | c.592-223A>G | EFHD2 | ENSG00000142634.13 | transcript | ENST00000375980.9 | protein_coding | 3/3 | chr1 | 15428370 |