Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 80303 |
| ensemblid | ENSG00000115468.13 |
| hgncid | 29556 |
| symbol | EFHD1 |
| name | EF-hand domain family member D1 |
| refseq_nuc | NM_025202.4 |
| refseq_prot | NP_079478.1 |
| ensembl_nuc | ENST00000264059.8 |
| ensembl_prot | ENSP00000264059.3 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 232633604 |
| end | 232682776 |
| strand | + |
| ver | v1.2 |
| region | chr2:232633604-232682776 |
| region5000 | chr2:232628604-232687776 |
| regionname0 | EFHD1_chr2_232633604_232682776 |
| regionname5000 | EFHD1_chr2_232628604_232687776 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 239 | 222 | 78 | 28 | 83 | 12 | 19 | 60 | EFHD1_chr2_232628604_232687776 | EFHD1 | MASEE others(234): Show |
chr2 | 232628604 | 232687776 |
| a0002 | 0/0 | 239 | 141 | 12 | 29 | 79 | 4 | 17 | 61 | EFHD1_chr2_232628604_232687776 | EFHD1 | MASEE others(234): Show |
chr2 | 232628604 | 232687776 |
| a0003 | 0/0 | 239 | 10 | 4 | 0 | 2 | 0 | 4 | 1 | EFHD1_chr2_232628604_232687776 | EFHD1 | MASEE others(234): Show |
chr2 | 232628604 | 232687776 |
| a0004 | 0/0 | 239 | 4 | 0 | 4 | 0 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | MASEE others(234): Show |
chr2 | 232628604 | 232687776 |
| a0005 | 0/0 | 239 | 2 | 0 | 1 | 0 | 0 | 1 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | MASEE others(234): Show |
chr2 | 232628604 | 232687776 |
| a0006 | 0/0 | 239 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | EFHD1_chr2_232628604_232687776 | EFHD1 | MASEE others(234): Show |
chr2 | 232628604 | 232687776 |
| a0007 | 0/0 | 239 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | EFHD1_chr2_232628604_232687776 | EFHD1 | MASEE others(234): Show |
chr2 | 232628604 | 232687776 |
| a0008 | 0/0 | 239 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | MASEE others(234): Show |
chr2 | 232628604 | 232687776 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 717 | 151 | 62 | 27 | 32 | 10 | 18 | EFHD1_chr2_232628604_232687776 | EFHD1 | ATGGC others(712): Show |
chr2 | 232628604 | 232687776 | ||
| a0001c0004 | 0/0 | 717 | 64 | 10 | 1 | 51 | 2 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | ATGGC others(712): Show |
chr2 | 232628604 | 232687776 | ||
| a0001c0006 | 0/0 | 717 | 5 | 5 | 0 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | ATGGC others(712): Show |
chr2 | 232628604 | 232687776 | ||
| a0001c0009 | 0/0 | 717 | 1 | 0 | 0 | 0 | 0 | 1 | EFHD1_chr2_232628604_232687776 | EFHD1 | ATGGC others(712): Show |
chr2 | 232628604 | 232687776 | ||
| a0001c0011 | 0/0 | 717 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | ATGGC others(712): Show |
chr2 | 232628604 | 232687776 | ||
| a0002c0002 | 0/0 | 717 | 72 | 8 | 22 | 25 | 4 | 13 | EFHD1_chr2_232628604_232687776 | EFHD1 | ATGGC others(712): Show |
chr2 | 232628604 | 232687776 | ||
| a0002c0003 | 0/0 | 717 | 69 | 4 | 7 | 54 | 0 | 4 | EFHD1_chr2_232628604_232687776 | EFHD1 | ATGGC others(712): Show |
chr2 | 232628604 | 232687776 | ||
| a0003c0005 | 0/0 | 717 | 10 | 4 | 0 | 2 | 0 | 4 | EFHD1_chr2_232628604_232687776 | EFHD1 | ATGGC others(712): Show |
chr2 | 232628604 | 232687776 | ||
| a0004c0007 | 0/0 | 717 | 4 | 0 | 4 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | ATGGC others(712): Show |
chr2 | 232628604 | 232687776 | ||
| a0005c0008 | 0/0 | 717 | 2 | 0 | 1 | 0 | 0 | 1 | EFHD1_chr2_232628604_232687776 | EFHD1 | ATGGC others(712): Show |
chr2 | 232628604 | 232687776 | ||
| a0006c0012 | 0/0 | 717 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | ATGGC others(712): Show |
chr2 | 232628604 | 232687776 | ||
| a0007c0010 | 0/0 | 717 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | ATGGC others(712): Show |
chr2 | 232628604 | 232687776 | ||
| a0008c0013 | 0/0 | 717 | 1 | 0 | 0 | 0 | 0 | 1 | EFHD1_chr2_232628604_232687776 | EFHD1 | ATGGC others(712): Show |
chr2 | 232628604 | 232687776 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 1878 | 17 | 8 | 3 | 5 | 0 | 1 | EFHD1_chr2_232628604_232687776 | EFHD1 | GGAGT others(1873): Show |
chr2 | 232628604 | 232687776 |
| a0001c0001t0002 | 0/1 | 1878 | 33 | 1 | 7 | 15 | 4 | 5 | EFHD1_chr2_232628604_232687776 | EFHD1 | GGAGT others(1873): Show |
chr2 | 232628604 | 232687776 |
| a0001c0001t0003 | 1/0 | 1878 | 39 | 11 | 14 | 1 | 4 | 8 | EFHD1_chr2_232628604_232687776 | EFHD1 | GGAGT others(1873): Show |
chr2 | 232628604 | 232687776 |
| a0001c0001t0004 | 0/0 | 1878 | 13 | 1 | 0 | 10 | 0 | 2 | EFHD1_chr2_232628604_232687776 | EFHD1 | GGAGT others(1873): Show |
chr2 | 232628604 | 232687776 |
| a0001c0001t0005 | 0/0 | 1878 | 11 | 9 | 0 | 0 | 1 | 1 | EFHD1_chr2_232628604_232687776 | EFHD1 | GGAGT others(1873): Show |
chr2 | 232628604 | 232687776 |
| a0001c0001t0006 | 0/0 | 1878 | 11 | 10 | 1 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | GGAGT others(1873): Show |
chr2 | 232628604 | 232687776 |
| a0001c0001t0007 | 0/0 | 1878 | 9 | 8 | 1 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | GGAGT others(1873): Show |
chr2 | 232628604 | 232687776 |
| a0001c0001t0008 | 0/0 | 1878 | 5 | 4 | 1 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | GGAGT others(1873): Show |
chr2 | 232628604 | 232687776 |
| a0001c0001t0009 | 0/0 | 1878 | 3 | 3 | 0 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | GGAGT others(1873): Show |
chr2 | 232628604 | 232687776 |
| a0001c0001t0010 | 0/0 | 1878 | 3 | 1 | 0 | 0 | 1 | 1 | EFHD1_chr2_232628604_232687776 | EFHD1 | GGAGT others(1873): Show |
chr2 | 232628604 | 232687776 |
| a0001c0001t0011 | 0/0 | 1878 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | GGAGT others(1873): Show |
chr2 | 232628604 | 232687776 |
| a0001c0001t0012 | 0/0 | 1902 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | GGAGA others(1897): Show |
chr2 | 232628604 | 232687776 |
| a0001c0001t0013 | 0/0 | 1878 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | GGAGT others(1873): Show |
chr2 | 232628604 | 232687776 |
| a0001c0001t0016 | 0/0 | 1851 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | GGAGT others(1846): Show |
chr2 | 232628604 | 232687776 |
| a0001c0001t0020 | 0/0 | 1878 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | GGAGT others(1873): Show |
chr2 | 232628604 | 232687776 |
| a0001c0001t0021 | 0/0 | 1878 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | GGAGT others(1873): Show |
chr2 | 232628604 | 232687776 |
| a0001c0001t0023 | 0/0 | 1878 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | GGAGT others(1873): Show |
chr2 | 232628604 | 232687776 |
| a0001c0004t0001 | 0/0 | 1878 | 6 | 2 | 1 | 3 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | GGAGT others(1873): Show |
chr2 | 232628604 | 232687776 |
| a0001c0004t0002 | 0/0 | 1878 | 20 | 1 | 0 | 18 | 1 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | GGAGT others(1873): Show |
chr2 | 232628604 | 232687776 |
| a0001c0004t0003 | 0/0 | 1878 | 15 | 0 | 0 | 15 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | GGAGT others(1873): Show |
chr2 | 232628604 | 232687776 |
| a0001c0004t0004 | 0/0 | 1878 | 18 | 2 | 0 | 15 | 1 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | GGAGT others(1873): Show |
chr2 | 232628604 | 232687776 |
| a0001c0004t0006 | 0/0 | 1878 | 5 | 5 | 0 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | GGAGT others(1873): Show |
chr2 | 232628604 | 232687776 |
| a0001c0006t0001 | 0/0 | 1878 | 2 | 2 | 0 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | GGAGT others(1873): Show |
chr2 | 232628604 | 232687776 |
| a0001c0006t0005 | 0/0 | 1878 | 3 | 3 | 0 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | GGAGT others(1873): Show |
chr2 | 232628604 | 232687776 |
| a0001c0009t0005 | 0/0 | 1878 | 1 | 0 | 0 | 0 | 0 | 1 | EFHD1_chr2_232628604_232687776 | EFHD1 | GGAGT others(1873): Show |
chr2 | 232628604 | 232687776 |
| a0001c0011t0003 | 0/0 | 1878 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | GGAGT others(1873): Show |
chr2 | 232628604 | 232687776 |
| a0002c0002t0001 | 0/0 | 1878 | 65 | 5 | 20 | 23 | 4 | 13 | EFHD1_chr2_232628604_232687776 | EFHD1 | GGAGT others(1873): Show |
chr2 | 232628604 | 232687776 |
| a0002c0002t0005 | 0/0 | 1878 | 4 | 2 | 1 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | GGAGT others(1873): Show |
chr2 | 232628604 | 232687776 |
| a0002c0002t0015 | 0/0 | 1878 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | GGAGT others(1873): Show |
chr2 | 232628604 | 232687776 |
| a0002c0002t0017 | 0/0 | 1878 | 1 | 0 | 1 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | GGAGT others(1873): Show |
chr2 | 232628604 | 232687776 |
| a0002c0002t0022 | 0/0 | 1878 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | GGAGT others(1873): Show |
chr2 | 232628604 | 232687776 |
| a0002c0003t0001 | 0/0 | 1878 | 66 | 4 | 7 | 53 | 0 | 2 | EFHD1_chr2_232628604_232687776 | EFHD1 | GGAGT others(1873): Show |
chr2 | 232628604 | 232687776 |
| a0002c0003t0014 | 0/0 | 1878 | 1 | 0 | 0 | 0 | 0 | 1 | EFHD1_chr2_232628604_232687776 | EFHD1 | GGAGT others(1873): Show |
chr2 | 232628604 | 232687776 |
| a0002c0003t0018 | 0/0 | 1878 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | GGAGT others(1873): Show |
chr2 | 232628604 | 232687776 |
| a0002c0003t0019 | 0/0 | 1878 | 1 | 0 | 0 | 0 | 0 | 1 | EFHD1_chr2_232628604_232687776 | EFHD1 | GGAGT others(1873): Show |
chr2 | 232628604 | 232687776 |
| a0003c0005t0001 | 0/0 | 1878 | 4 | 0 | 0 | 1 | 0 | 3 | EFHD1_chr2_232628604_232687776 | EFHD1 | GGAGT others(1873): Show |
chr2 | 232628604 | 232687776 |
| a0003c0005t0002 | 0/0 | 1878 | 3 | 1 | 0 | 1 | 0 | 1 | EFHD1_chr2_232628604_232687776 | EFHD1 | GGAGT others(1873): Show |
chr2 | 232628604 | 232687776 |
| a0003c0005t0006 | 0/0 | 1878 | 2 | 2 | 0 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | GGAGT others(1873): Show |
chr2 | 232628604 | 232687776 |
| a0003c0005t0011 | 0/0 | 1878 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | GGAGT others(1873): Show |
chr2 | 232628604 | 232687776 |
| a0004c0007t0001 | 0/0 | 1878 | 4 | 0 | 4 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | GGAGT others(1873): Show |
chr2 | 232628604 | 232687776 |
| a0005c0008t0001 | 0/0 | 1878 | 2 | 0 | 1 | 0 | 0 | 1 | EFHD1_chr2_232628604_232687776 | EFHD1 | GGAGT others(1873): Show |
chr2 | 232628604 | 232687776 |
| a0006c0012t0001 | 0/0 | 1878 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | GGAGT others(1873): Show |
chr2 | 232628604 | 232687776 |
| a0007c0010t0001 | 0/0 | 1878 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | GGAGT others(1873): Show |
chr2 | 232628604 | 232687776 |
| a0008c0013t0001 | 0/0 | 1878 | 1 | 0 | 0 | 0 | 0 | 1 | EFHD1_chr2_232628604_232687776 | EFHD1 | GGAGT others(1873): Show |
chr2 | 232628604 | 232687776 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0001g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0002g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0002g0174 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0002g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0002g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0002g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0002g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0002g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0002g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0002g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0002g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0002g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0002g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0002g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0002g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0002g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0002g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0002g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0002g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0002g0367 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0002g0368 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0003g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0003g0008 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0003g0014 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0003g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0003g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0003g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0003g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0003g0145 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0003g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0003g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0003g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0003g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0003g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0003g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0003g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0003g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0003g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0003g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0003g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0003g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0003g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0003g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0003g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0003g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0003g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0003g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0003g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0003g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0003g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0003g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0003g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0003g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0003g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0003g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0003g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0003g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0003g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0004g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0004g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0004g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0004g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0004g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0004g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0004g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0004g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0004g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0004g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0004g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0004g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0004g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0005g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0005g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0005g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0005g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0005g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0005g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0005g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0005g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0005g0303 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0005g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0006g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0006g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0006g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0006g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0006g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0006g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0006g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0006g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0006g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0006g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0006g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0007g0002 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0007g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0007g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0007g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0007g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0007g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0007g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0008g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0008g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0008g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0008g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0008g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0009g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0009g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0009g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0010g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0010g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0010g0306 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0011g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0012g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0013g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0016g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0020g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0021g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0001t0023g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0004t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0004t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0004t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0004t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0004t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0004t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0004t0002g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0004t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0004t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0004t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0004t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0004t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0004t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0004t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0004t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0004t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0004t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0004t0002g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0004t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0004t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0004t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0004t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0004t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0004t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0004t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0004t0002g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0004t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0004t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0004t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0004t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0004t0003g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0004t0003g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0004t0003g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0004t0003g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0004t0003g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0004t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0004t0003g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0004t0003g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0004t0003g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0004t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0004t0003g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0004t0004g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0004t0004g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0004t0004g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0004t0004g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0004t0004g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0004t0004g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0004t0004g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0004t0004g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0004t0004g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0004t0004g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0004t0004g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0004t0004g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0004t0004g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0004t0004g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0004t0004g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0004t0004g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0004t0004g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0004t0004g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0004t0006g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0004t0006g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0004t0006g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0004t0006g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0006t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0006t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0006t0005g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0006t0005g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0006t0005g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0009t0005g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0001c0011t0003g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0002c0002t0001g0001 | 0/0 | 4 | 1 | 2 | 0 | 0 | 1 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0002c0002t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0002c0002t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0002c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0002c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0002c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0002c0002t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0002c0002t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0002c0002t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0002c0002t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0002c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0002c0002t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0002c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0002c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0002c0002t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0002c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0002c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0002c0002t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0002c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0002c0002t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0002c0002t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0002c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0002c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0002c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0002c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0002c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0002c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0002c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0002c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0002c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0002c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0002c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0002c0002t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0002c0002t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0002c0002t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0002c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0002c0002t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0002c0002t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0002c0002t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0002c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0002c0002t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0002c0002t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0002c0002t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0002c0002t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0002c0002t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0002c0002t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0002c0002t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0002c0002t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0002c0002t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0002c0002t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0002c0002t0001g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0002c0002t0001g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0002c0002t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0002c0002t0001g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0002c0002t0001g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0002c0002t0001g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0002c0002t0001g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0002c0002t0001g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0002c0002t0001g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0002c0002t0001g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0002c0002t0001g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0002c0002t0005g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0002c0002t0005g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0002c0002t0005g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0002c0002t0005g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0002c0002t0015g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0002c0002t0017g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0002c0002t0022g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0002c0003t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0002c0003t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0002c0003t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0002c0003t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0002c0003t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0002c0003t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0002c0003t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0002c0003t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0002c0003t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0002c0003t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0002c0003t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0002c0003t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0002c0003t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0002c0003t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0002c0003t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0002c0003t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0002c0003t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0002c0003t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0002c0003t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0002c0003t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0002c0003t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0002c0003t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0002c0003t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0002c0003t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0002c0003t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0002c0003t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0002c0003t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0002c0003t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0002c0003t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0002c0003t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0002c0003t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0002c0003t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0002c0003t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0002c0003t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0002c0003t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0002c0003t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0002c0003t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0002c0003t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0002c0003t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0002c0003t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0002c0003t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0002c0003t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0002c0003t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0002c0003t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0002c0003t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0002c0003t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0002c0003t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0002c0003t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0002c0003t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0002c0003t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0002c0003t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0002c0003t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0002c0003t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0002c0003t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0002c0003t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0002c0003t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0002c0003t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0002c0003t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0002c0003t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0002c0003t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0002c0003t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0002c0003t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0002c0003t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0002c0003t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0002c0003t0014g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0002c0003t0018g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0002c0003t0019g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0003c0005t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0003c0005t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0003c0005t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0003c0005t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0003c0005t0002g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0003c0005t0002g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0003c0005t0002g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0003c0005t0006g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0003c0005t0006g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0003c0005t0011g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0004c0007t0001g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0004c0007t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0004c0007t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0005c0008t0001g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0005c0008t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0006c0012t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0007c0010t0001g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| a0008c0013t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0002 | t0001 | g0229 | EUR | GBR | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG00099 | hp2 | a0001 | c0001 | t0003 | g0014 | EUR | GBR | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG00140 | hp1 | a0002 | c0002 | t0001 | g0254 | EUR | GBR | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG00140 | hp2 | a0001 | c0004 | t0002 | g0136 | EUR | GBR | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG00280 | hp1 | a0001 | c0001 | t0010 | g0306 | EUR | FIN | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG00280 | hp2 | a0002 | c0002 | t0001 | g0176 | EUR | FIN | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG00323 | hp1 | a0001 | c0004 | t0004 | g0171 | EUR | FIN | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG00323 | hp2 | a0002 | c0002 | t0001 | g0199 | EUR | FIN | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG00408 | hp1 | a0002 | c0003 | t0001 | g0166 | EAS | CHS | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG00408 | hp2 | a0001 | c0004 | t0004 | g0104 | EAS | CHS | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0355 | EAS | CHS | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG00423 | hp2 | a0002 | c0002 | t0001 | g0011 | EAS | CHS | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG00438 | hp1 | a0002 | c0002 | t0001 | g0348 | EAS | CHS | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG00438 | hp2 | a0002 | c0003 | t0001 | g0074 | EAS | CHS | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG00544 | hp1 | a0002 | c0002 | t0001 | g0314 | EAS | CHS | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | CHS | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG00558 | hp1 | a0001 | c0004 | t0002 | g0134 | EAS | CHS | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG00558 | hp2 | a0002 | c0003 | t0001 | g0092 | EAS | CHS | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG00597 | hp1 | a0001 | c0001 | t0004 | g0159 | EAS | CHS | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG00597 | hp2 | a0002 | c0003 | t0001 | g0084 | EAS | CHS | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG00609 | hp1 | a0001 | c0004 | t0001 | g0223 | EAS | CHS | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG00609 | hp2 | a0001 | c0001 | t0003 | g0245 | EAS | CHS | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG00621 | hp1 | a0001 | c0004 | t0002 | g0128 | EAS | CHS | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0343 | EAS | CHS | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG00642 | hp1 | a0002 | c0002 | t0005 | g0302 | AMR | PUR | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG00642 | hp2 | a0002 | c0003 | t0001 | g0261 | AMR | PUR | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG00673 | hp1 | a0002 | c0002 | t0001 | g0363 | EAS | CHS | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG00673 | hp2 | a0002 | c0003 | t0001 | g0080 | EAS | CHS | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0142 | AMR | PUR | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG00733 | hp2 | a0004 | c0007 | t0001 | g0217 | AMR | PUR | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG00735 | hp1 | a0004 | c0007 | t0001 | g0006 | AMR | PUR | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG00735 | hp2 | a0002 | c0002 | t0001 | g0233 | AMR | PUR | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG00738 | hp1 | a0001 | c0001 | t0003 | g0243 | AMR | PUR | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG00738 | hp2 | a0001 | c0001 | t0003 | g0240 | AMR | PUR | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG00741 | hp1 | a0002 | c0002 | t0001 | g0144 | AMR | PUR | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG00741 | hp2 | a0002 | c0002 | t0001 | g0106 | AMR | PUR | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG01070 | hp1 | a0001 | c0001 | t0003 | g0236 | AMR | PUR | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG01070 | hp2 | a0001 | c0001 | t0003 | g0234 | AMR | PUR | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG01074 | hp1 | a0002 | c0002 | t0001 | g0192 | AMR | PUR | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG01074 | hp2 | a0004 | c0007 | t0001 | g0006 | AMR | PUR | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG01081 | hp1 | a0001 | c0001 | t0003 | g0247 | AMR | PUR | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG01081 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG01099 | hp1 | a0001 | c0004 | t0001 | g0057 | AMR | PUR | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG01099 | hp2 | a0004 | c0007 | t0001 | g0218 | AMR | PUR | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0181 | AMR | PUR | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG01109 | hp1 | a0002 | c0002 | t0001 | g0232 | AMR | PUR | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG01109 | hp2 | a0001 | c0001 | t0006 | g0035 | AMR | PUR | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG01167 | hp1 | a0002 | c0002 | t0001 | g0053 | AMR | PUR | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG01167 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0155 | AMR | PUR | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG01175 | hp2 | a0001 | c0001 | t0007 | g0304 | AMR | PUR | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG01243 | hp1 | a0001 | c0001 | t0008 | g0283 | AMR | PUR | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG01243 | hp2 | a0002 | c0003 | t0001 | g0110 | AMR | PUR | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG01255 | hp1 | a0002 | c0003 | t0001 | g0260 | AMR | CLM | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0252 | AMR | CLM | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG01256 | hp1 | a0002 | c0002 | t0001 | g0328 | AMR | CLM | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG01256 | hp2 | a0001 | c0001 | t0003 | g0007 | AMR | CLM | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG01258 | hp1 | a0001 | c0001 | t0003 | g0256 | AMR | CLM | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG01258 | hp2 | a0001 | c0001 | t0003 | g0007 | AMR | CLM | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG01261 | hp1 | a0001 | c0001 | t0003 | g0251 | AMR | CLM | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG01261 | hp2 | a0002 | c0002 | t0001 | g0175 | AMR | CLM | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | CLM | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG01346 | hp2 | a0002 | c0003 | t0001 | g0066 | AMR | CLM | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG01361 | hp1 | a0001 | c0001 | t0003 | g0248 | AMR | CLM | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG01361 | hp2 | a0001 | c0001 | t0003 | g0336 | AMR | CLM | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0118 | AMR | CLM | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG01433 | hp2 | a0005 | c0008 | t0001 | g0022 | AMR | CLM | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG01496 | hp1 | a0002 | c0003 | t0001 | g0107 | AMR | CLM | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0367 | AMR | CLM | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0258 | EUR | IBS | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG01516 | hp2 | a0001 | c0001 | t0003 | g0238 | EUR | IBS | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG01517 | hp1 | a0001 | c0001 | t0003 | g0241 | EUR | IBS | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0253 | EUR | IBS | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG01884 | hp1 | a0002 | c0002 | t0005 | g0292 | AFR | ACB | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG01884 | hp2 | a0001 | c0001 | t0003 | g0237 | AFR | ACB | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG01891 | hp1 | a0001 | c0001 | t0008 | g0289 | AFR | ACB | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG01891 | hp2 | a0001 | c0001 | t0005 | g0364 | AFR | ACB | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG01934 | hp1 | a0002 | c0002 | t0001 | g0337 | AMR | PEL | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG01934 | hp2 | a0002 | c0002 | t0001 | g0054 | AMR | PEL | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG01952 | hp1 | a0002 | c0002 | t0001 | g0330 | AMR | PEL | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0368 | AMR | PEL | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG01975 | hp1 | a0002 | c0002 | t0017 | g0311 | AMR | PEL | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG01975 | hp2 | a0002 | c0002 | t0001 | g0345 | AMR | PEL | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG01981 | hp1 | a0002 | c0002 | t0001 | g0342 | AMR | PEL | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG01981 | hp2 | a0002 | c0002 | t0001 | g0340 | AMR | PEL | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG01993 | hp1 | a0002 | c0003 | t0001 | g0109 | AMR | PEL | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG01993 | hp2 | a0001 | c0001 | t0003 | g0056 | AMR | PEL | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG02027 | hp1 | a0001 | c0004 | t0003 | g0063 | EAS | KHV | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG02027 | hp2 | a0002 | c0002 | t0001 | g0317 | EAS | KHV | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG02040 | hp1 | a0001 | c0004 | t0002 | g0113 | EAS | KHV | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG02040 | hp2 | a0001 | c0004 | t0002 | g0114 | EAS | KHV | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | ACB | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0246 | AFR | ACB | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG02056 | hp1 | a0001 | c0001 | t0004 | g0344 | EAS | KHV | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG02056 | hp2 | a0002 | c0002 | t0001 | g0206 | EAS | KHV | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG02071 | hp1 | a0002 | c0002 | t0001 | g0331 | EAS | KHV | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG02071 | hp2 | a0001 | c0004 | t0002 | g0140 | EAS | KHV | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG02074 | hp1 | a0002 | c0003 | t0001 | g0115 | EAS | KHV | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0347 | EAS | KHV | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG02083 | hp1 | a0002 | c0003 | t0018 | g0005 | EAS | KHV | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0315 | EAS | KHV | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG02129 | hp1 | a0001 | c0001 | t0004 | g0329 | EAS | KHV | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG02129 | hp2 | a0003 | c0005 | t0002 | g0018 | EAS | KHV | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG02132 | hp1 | a0001 | c0004 | t0002 | g0138 | EAS | KHV | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG02132 | hp2 | a0002 | c0002 | t0005 | g0362 | EAS | KHV | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG02135 | hp1 | a0002 | c0003 | t0001 | g0209 | EAS | KHV | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG02135 | hp2 | a0001 | c0004 | t0003 | g0082 | EAS | KHV | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG02145 | hp1 | a0001 | c0001 | t0003 | g0357 | AFR | ACB | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG02145 | hp2 | a0001 | c0001 | t0003 | g0037 | AFR | ACB | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG02148 | hp1 | a0002 | c0002 | t0001 | g0226 | AMR | PEL | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG02148 | hp2 | a0001 | c0001 | t0003 | g0360 | AMR | PEL | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG02155 | hp1 | a0001 | c0004 | t0003 | g0094 | EAS | CDX | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG02155 | hp2 | a0002 | c0003 | t0001 | g0069 | EAS | CDX | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG02257 | hp1 | a0001 | c0001 | t0007 | g0290 | AFR | ACB | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG02257 | hp2 | a0001 | c0001 | t0008 | g0287 | AFR | ACB | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG02258 | hp1 | a0002 | c0003 | t0001 | g0126 | AFR | ACB | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG02258 | hp2 | a0003 | c0005 | t0006 | g0058 | AFR | ACB | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG02280 | hp1 | a0001 | c0001 | t0006 | g0026 | AFR | ACB | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG02280 | hp2 | a0001 | c0001 | t0007 | g0002 | AFR | ACB | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG02293 | hp1 | a0001 | c0001 | t0003 | g0335 | AMR | PEL | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | PEL | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG02300 | hp1 | a0002 | c0002 | t0001 | g0047 | AMR | PEL | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG02300 | hp2 | a0002 | c0002 | t0001 | g0055 | AMR | PEL | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG02451 | hp1 | a0001 | c0001 | t0003 | g0235 | AFR | ACB | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG02451 | hp2 | a0001 | c0001 | t0005 | g0286 | AFR | ACB | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG02523 | hp1 | a0001 | c0001 | t0004 | g0359 | EAS | KHV | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG02523 | hp2 | a0001 | c0004 | t0004 | g0105 | EAS | KHV | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG02572 | hp1 | a0001 | c0001 | t0007 | g0296 | AFR | GWD | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0308 | AFR | GWD | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG02602 | hp1 | a0002 | c0002 | t0001 | g0255 | SAS | PJL | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG02602 | hp2 | a0001 | c0001 | t0003 | g0239 | SAS | PJL | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG02615 | hp1 | a0001 | c0001 | t0004 | g0031 | AFR | GWD | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG02615 | hp2 | a0001 | c0001 | t0005 | g0293 | AFR | GWD | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG02622 | hp1 | a0001 | c0001 | t0009 | g0271 | AFR | GWD | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG02622 | hp2 | a0001 | c0001 | t0006 | g0098 | AFR | GWD | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG02630 | hp1 | a0001 | c0001 | t0021 | g0272 | AFR | GWD | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG02630 | hp2 | a0002 | c0002 | t0001 | g0279 | AFR | GWD | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG02647 | hp1 | a0002 | c0002 | t0001 | g0215 | AFR | GWD | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG02647 | hp2 | a0001 | c0001 | t0006 | g0361 | AFR | GWD | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG02683 | hp1 | a0005 | c0008 | t0001 | g0020 | SAS | PJL | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG02683 | hp2 | a0003 | c0005 | t0001 | g0028 | SAS | PJL | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG02698 | hp1 | a0002 | c0002 | t0001 | g0213 | SAS | PJL | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG02698 | hp2 | a0001 | c0001 | t0004 | g0177 | SAS | PJL | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG02723 | hp1 | a0003 | c0005 | t0011 | g0023 | AFR | GWD | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG02723 | hp2 | a0001 | c0001 | t0007 | g0291 | AFR | GWD | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG02735 | hp1 | a0001 | c0001 | t0010 | g0301 | SAS | PJL | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG02735 | hp2 | a0002 | c0002 | t0001 | g0198 | SAS | PJL | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG02738 | hp1 | a0002 | c0003 | t0001 | g0067 | SAS | PJL | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG02738 | hp2 | a0001 | c0001 | t0003 | g0231 | SAS | PJL | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG02809 | hp1 | a0001 | c0001 | t0007 | g0002 | AFR | GWD | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG02809 | hp2 | a0002 | c0002 | t0005 | g0284 | AFR | GWD | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG02818 | hp1 | a0001 | c0004 | t0006 | g0191 | AFR | GWD | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG02818 | hp2 | a0001 | c0001 | t0006 | g0269 | AFR | GWD | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG02886 | hp1 | a0001 | c0001 | t0023 | g0309 | AFR | GWD | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG02886 | hp2 | a0001 | c0001 | t0006 | g0025 | AFR | GWD | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG02895 | hp1 | a0001 | c0001 | t0007 | g0305 | AFR | GWD | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG02895 | hp2 | a0001 | c0001 | t0006 | g0278 | AFR | GWD | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG02896 | hp1 | a0001 | c0001 | t0003 | g0275 | AFR | GWD | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG02896 | hp2 | a0002 | c0002 | t0001 | g0280 | AFR | GWD | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG02897 | hp1 | a0001 | c0001 | t0003 | g0270 | AFR | GWD | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG02897 | hp2 | a0001 | c0001 | t0006 | g0277 | AFR | GWD | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG02922 | hp1 | a0001 | c0001 | t0006 | g0030 | AFR | ESN | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG02922 | hp2 | a0001 | c0001 | t0006 | g0097 | AFR | ESN | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG02965 | hp1 | a0001 | c0006 | t0001 | g0267 | AFR | ESN | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG02965 | hp2 | a0001 | c0004 | t0001 | g0157 | AFR | ESN | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG02976 | hp1 | a0001 | c0001 | t0003 | g0268 | AFR | ESN | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG02976 | hp2 | a0001 | c0001 | t0003 | g0307 | AFR | ESN | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | GWD | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG03041 | hp2 | a0001 | c0004 | t0004 | g0164 | AFR | GWD | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG03098 | hp1 | a0001 | c0001 | t0020 | g0276 | AFR | MSL | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG03098 | hp2 | a0001 | c0004 | t0002 | g0262 | AFR | MSL | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG03130 | hp1 | a0001 | c0001 | t0008 | g0294 | AFR | ESN | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG03130 | hp2 | a0001 | c0006 | t0005 | g0365 | AFR | ESN | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG03139 | hp1 | a0003 | c0005 | t0002 | g0015 | AFR | ESN | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG03139 | hp2 | a0002 | c0003 | t0001 | g0120 | AFR | ESN | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG03195 | hp1 | a0001 | c0001 | t0013 | g0039 | AFR | ESN | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG03195 | hp2 | a0001 | c0006 | t0001 | g0034 | AFR | ESN | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG03209 | hp1 | a0001 | c0001 | t0003 | g0266 | AFR | MSL | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG03209 | hp2 | a0001 | c0001 | t0010 | g0298 | AFR | MSL | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG03225 | hp1 | a0001 | c0001 | t0003 | g0228 | AFR | MSL | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG03225 | hp2 | a0001 | c0004 | t0006 | g0009 | AFR | MSL | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG03239 | hp1 | a0001 | c0001 | t0005 | g0300 | SAS | PJL | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG03239 | hp2 | a0001 | c0001 | t0003 | g0244 | SAS | PJL | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG03453 | hp1 | a0001 | c0001 | t0005 | g0282 | AFR | MSL | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG03453 | hp2 | a0001 | c0001 | t0007 | g0295 | AFR | MSL | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG03486 | hp1 | a0001 | c0001 | t0009 | g0273 | AFR | MSL | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG03486 | hp2 | a0001 | c0001 | t0007 | g0002 | AFR | MSL | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG03490 | hp1 | a0003 | c0005 | t0001 | g0021 | SAS | PJL | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG03490 | hp2 | a0001 | c0001 | t0003 | g0008 | SAS | PJL | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG03492 | hp1 | a0002 | c0002 | t0001 | g0205 | SAS | PJL | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG03492 | hp2 | a0001 | c0001 | t0003 | g0008 | SAS | PJL | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG03516 | hp1 | a0001 | c0001 | t0011 | g0038 | AFR | ESN | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG03516 | hp2 | a0001 | c0004 | t0001 | g0182 | AFR | ESN | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0265 | AFR | GWD | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG03540 | hp2 | a0003 | c0005 | t0006 | g0259 | AFR | GWD | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG03579 | hp1 | a0001 | c0001 | t0005 | g0281 | AFR | MSL | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0356 | AFR | MSL | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG03654 | hp1 | a0003 | c0005 | t0002 | g0060 | SAS | PJL | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG03654 | hp2 | a0001 | c0001 | t0004 | g0178 | SAS | PJL | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG03669 | hp1 | a0002 | c0002 | t0001 | g0257 | SAS | PJL | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG03669 | hp2 | a0001 | c0009 | t0005 | g0299 | SAS | PJL | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0321 | SAS | STU | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0013 | SAS | STU | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG03704 | hp1 | a0002 | c0002 | t0001 | g0132 | SAS | PJL | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG03704 | hp2 | a0002 | c0003 | t0019 | g0129 | SAS | PJL | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG03710 | hp1 | a0001 | c0001 | t0003 | g0119 | SAS | PJL | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG03710 | hp2 | a0002 | c0002 | t0001 | g0001 | SAS | PJL | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG03831 | hp1 | a0003 | c0005 | t0001 | g0029 | SAS | BEB | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG03831 | hp2 | a0002 | c0003 | t0014 | g0116 | SAS | BEB | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG03834 | hp1 | a0002 | c0002 | t0001 | g0040 | SAS | BEB | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG03834 | hp2 | a0002 | c0002 | t0001 | g0173 | SAS | BEB | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0194 | SAS | BEB | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0219 | SAS | BEB | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0222 | SAS | BEB | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG04184 | hp2 | a0002 | c0002 | t0001 | g0204 | SAS | BEB | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0203 | SAS | STU | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG04199 | hp2 | a0002 | c0003 | t0001 | g0149 | SAS | STU | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG04204 | hp1 | a0002 | c0002 | t0001 | g0197 | SAS | STU | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG04204 | hp2 | a0002 | c0002 | t0001 | g0150 | SAS | STU | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG04228 | hp1 | a0001 | c0001 | t0003 | g0250 | SAS | STU | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG04228 | hp2 | a0002 | c0002 | t0001 | g0195 | SAS | STU | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA18522 | hp1 | a0002 | c0002 | t0022 | g0263 | AFR | YRI | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | YRI | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA18747 | hp1 | a0002 | c0003 | t0001 | g0072 | EAS | CHB | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA18747 | hp2 | a0001 | c0004 | t0004 | g0230 | EAS | CHB | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA18906 | hp1 | a0001 | c0004 | t0004 | g0165 | AFR | YRI | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA18906 | hp2 | a0001 | c0004 | t0006 | g0042 | AFR | YRI | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA18939 | hp1 | a0002 | c0003 | t0001 | g0153 | EAS | JPT | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA18939 | hp2 | a0001 | c0004 | t0003 | g0083 | EAS | JPT | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA18941 | hp1 | a0006 | c0012 | t0001 | g0100 | EAS | JPT | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA18941 | hp2 | a0002 | c0003 | t0001 | g0112 | EAS | JPT | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA18942 | hp1 | a0002 | c0002 | t0001 | g0201 | EAS | JPT | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA18942 | hp2 | a0001 | c0004 | t0004 | g0169 | EAS | JPT | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA18944 | hp1 | a0001 | c0004 | t0003 | g0186 | EAS | JPT | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA18944 | hp2 | a0002 | c0003 | t0001 | g0093 | EAS | JPT | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0341 | EAS | JPT | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA18945 | hp2 | a0001 | c0004 | t0003 | g0185 | EAS | JPT | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA18946 | hp1 | a0001 | c0004 | t0003 | g0187 | EAS | JPT | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA18946 | hp2 | a0002 | c0002 | t0001 | g0011 | EAS | JPT | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA18947 | hp1 | a0001 | c0001 | t0004 | g0338 | EAS | JPT | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA18947 | hp2 | a0002 | c0003 | t0001 | g0124 | EAS | JPT | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0325 | EAS | JPT | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA18948 | hp2 | a0002 | c0002 | t0001 | g0310 | EAS | JPT | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA18950 | hp1 | a0001 | c0004 | t0004 | g0154 | EAS | JPT | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA18950 | hp2 | a0002 | c0003 | t0001 | g0085 | EAS | JPT | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA18951 | hp1 | a0001 | c0004 | t0004 | g0081 | EAS | JPT | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA18952 | hp1 | a0002 | c0002 | t0001 | g0312 | EAS | JPT | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA18952 | hp2 | a0002 | c0003 | t0001 | g0089 | EAS | JPT | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0332 | EAS | JPT | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA18954 | hp2 | a0002 | c0002 | t0001 | g0044 | EAS | JPT | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA18957 | hp1 | a0007 | c0010 | t0001 | g0346 | EAS | JPT | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0324 | EAS | JPT | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA18959 | hp1 | a0001 | c0004 | t0003 | g0224 | EAS | JPT | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA18959 | hp2 | a0002 | c0003 | t0001 | g0088 | EAS | JPT | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA18960 | hp1 | a0001 | c0004 | t0003 | g0183 | EAS | JPT | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0339 | EAS | JPT | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA18962 | hp1 | a0002 | c0003 | t0001 | g0193 | EAS | JPT | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA18962 | hp2 | a0001 | c0004 | t0003 | g0061 | EAS | JPT | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA18966 | hp1 | a0002 | c0002 | t0001 | g0045 | EAS | JPT | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA18966 | hp2 | a0002 | c0003 | t0001 | g0158 | EAS | JPT | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA18967 | hp1 | a0001 | c0004 | t0002 | g0141 | EAS | JPT | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA18967 | hp2 | a0002 | c0002 | t0001 | g0046 | EAS | JPT | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA18969 | hp1 | a0002 | c0003 | t0001 | g0003 | EAS | JPT | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA18969 | hp2 | a0001 | c0004 | t0004 | g0207 | EAS | JPT | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA18970 | hp1 | a0001 | c0004 | t0002 | g0139 | EAS | JPT | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA18970 | hp2 | a0002 | c0003 | t0001 | g0212 | EAS | JPT | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA18971 | hp1 | a0002 | c0003 | t0001 | g0152 | EAS | JPT | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA18971 | hp2 | a0001 | c0004 | t0004 | g0208 | EAS | JPT | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA18972 | hp1 | a0001 | c0004 | t0002 | g0151 | EAS | JPT | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA18972 | hp2 | a0001 | c0004 | t0004 | g0064 | EAS | JPT | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA18973 | hp1 | a0001 | c0004 | t0002 | g0131 | EAS | JPT | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA18973 | hp2 | a0002 | c0003 | t0001 | g0086 | EAS | JPT | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA18975 | hp1 | a0002 | c0003 | t0001 | g0068 | EAS | JPT | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA18975 | hp2 | a0002 | c0003 | t0001 | g0125 | EAS | JPT | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA18979 | hp1 | a0001 | c0004 | t0003 | g0190 | EAS | JPT | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA18979 | hp2 | a0001 | c0004 | t0002 | g0225 | EAS | JPT | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA18980 | hp1 | a0002 | c0003 | t0001 | g0101 | EAS | JPT | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA18980 | hp2 | a0002 | c0003 | t0001 | g0005 | EAS | JPT | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA18981 | hp1 | a0001 | c0001 | t0004 | g0352 | EAS | JPT | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA18981 | hp2 | a0001 | c0004 | t0001 | g0221 | EAS | JPT | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA18983 | hp1 | a0001 | c0004 | t0002 | g0062 | EAS | JPT | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA18983 | hp2 | a0002 | c0003 | t0001 | g0122 | EAS | JPT | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA18986 | hp1 | a0002 | c0003 | t0001 | g0090 | EAS | JPT | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA18986 | hp2 | a0002 | c0003 | t0001 | g0137 | EAS | JPT | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA18988 | hp1 | a0001 | c0001 | t0002 | g0200 | EAS | JPT | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA18988 | hp2 | a0002 | c0002 | t0001 | g0102 | EAS | JPT | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA18989 | hp1 | a0001 | c0004 | t0004 | g0147 | EAS | JPT | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA18989 | hp2 | a0003 | c0005 | t0001 | g0017 | EAS | JPT | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA18990 | hp1 | a0001 | c0004 | t0002 | g0078 | EAS | JPT | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA18990 | hp2 | a0001 | c0004 | t0002 | g0095 | EAS | JPT | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA18994 | hp1 | a0001 | c0004 | t0002 | g0127 | EAS | JPT | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA18994 | hp2 | a0002 | c0002 | t0001 | g0358 | EAS | JPT | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA18995 | hp1 | a0001 | c0004 | t0003 | g0071 | EAS | JPT | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0333 | EAS | JPT | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA18997 | hp2 | a0002 | c0003 | t0001 | g0075 | EAS | JPT | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA18998 | hp1 | a0001 | c0004 | t0001 | g0167 | EAS | JPT | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA18998 | hp2 | a0001 | c0004 | t0004 | g0135 | EAS | JPT | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA18999 | hp2 | a0002 | c0003 | t0001 | g0087 | EAS | JPT | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA19000 | hp1 | a0002 | c0003 | t0001 | g0160 | EAS | JPT | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA19000 | hp2 | a0002 | c0003 | t0001 | g0076 | EAS | JPT | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA19003 | hp1 | a0002 | c0003 | t0001 | g0004 | EAS | JPT | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA19003 | hp2 | a0002 | c0002 | t0001 | g0350 | EAS | JPT | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA19004 | hp1 | a0002 | c0003 | t0001 | g0210 | EAS | JPT | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA19004 | hp2 | a0001 | c0004 | t0003 | g0184 | EAS | JPT | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA19009 | hp1 | a0001 | c0004 | t0002 | g0130 | EAS | JPT | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA19009 | hp2 | a0002 | c0003 | t0001 | g0004 | EAS | JPT | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA19010 | hp1 | a0002 | c0003 | t0001 | g0123 | EAS | JPT | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA19010 | hp2 | a0002 | c0002 | t0001 | g0316 | EAS | JPT | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA19011 | hp1 | a0002 | c0003 | t0001 | g0161 | EAS | JPT | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA19011 | hp2 | a0002 | c0003 | t0001 | g0148 | EAS | JPT | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA19012 | hp1 | a0001 | c0004 | t0004 | g0146 | EAS | JPT | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0322 | EAS | JPT | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA19030 | hp1 | a0001 | c0001 | t0003 | g0032 | AFR | LWK | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA19030 | hp2 | a0001 | c0004 | t0006 | g0041 | AFR | LWK | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA19043 | hp1 | a0001 | c0006 | t0005 | g0366 | AFR | LWK | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA19043 | hp2 | a0002 | c0003 | t0001 | g0220 | AFR | LWK | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA19055 | hp1 | a0001 | c0004 | t0002 | g0016 | EAS | JPT | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA19055 | hp2 | a0002 | c0003 | t0001 | g0196 | EAS | JPT | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA19056 | hp1 | a0001 | c0001 | t0012 | g0351 | EAS | JPT | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA19056 | hp2 | a0002 | c0002 | t0001 | g0327 | EAS | JPT | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA19060 | hp1 | a0001 | c0004 | t0004 | g0065 | EAS | JPT | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA19060 | hp2 | a0001 | c0001 | t0004 | g0354 | EAS | JPT | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA19062 | hp1 | a0002 | c0002 | t0015 | g0313 | EAS | JPT | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA19062 | hp2 | a0001 | c0001 | t0002 | g0326 | EAS | JPT | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA19064 | hp1 | a0002 | c0003 | t0001 | g0156 | EAS | JPT | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA19064 | hp2 | a0002 | c0002 | t0001 | g0143 | EAS | JPT | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA19065 | hp1 | a0001 | c0004 | t0004 | g0168 | EAS | JPT | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA19065 | hp2 | a0002 | c0003 | t0001 | g0003 | EAS | JPT | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA19068 | hp1 | a0002 | c0003 | t0001 | g0073 | EAS | JPT | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA19068 | hp2 | a0002 | c0003 | t0001 | g0211 | EAS | JPT | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA19074 | hp1 | a0002 | c0003 | t0001 | g0133 | EAS | JPT | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0334 | EAS | JPT | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA19077 | hp1 | a0002 | c0003 | t0001 | g0070 | EAS | JPT | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA19077 | hp2 | a0001 | c0004 | t0004 | g0103 | EAS | JPT | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA19081 | hp1 | a0001 | c0004 | t0003 | g0188 | EAS | JPT | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0349 | EAS | JPT | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA19083 | hp1 | a0002 | c0003 | t0001 | g0059 | EAS | JPT | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA19083 | hp2 | a0001 | c0001 | t0004 | g0320 | EAS | JPT | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA19084 | hp1 | a0002 | c0003 | t0001 | g0096 | EAS | JPT | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA19084 | hp2 | a0002 | c0003 | t0001 | g0189 | EAS | JPT | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA19085 | hp1 | a0002 | c0002 | t0001 | g0318 | EAS | JPT | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA19085 | hp2 | a0001 | c0001 | t0004 | g0319 | EAS | JPT | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA19086 | hp1 | a0001 | c0004 | t0002 | g0162 | EAS | JPT | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA19086 | hp2 | a0002 | c0002 | t0001 | g0202 | EAS | JPT | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA19087 | hp1 | a0002 | c0003 | t0001 | g0163 | EAS | JPT | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA19087 | hp2 | a0001 | c0001 | t0004 | g0353 | EAS | JPT | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0323 | EAS | JPT | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA19088 | hp2 | a0002 | c0002 | t0001 | g0214 | EAS | JPT | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA19089 | hp1 | a0001 | c0004 | t0003 | g0111 | EAS | JPT | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA19089 | hp2 | a0002 | c0003 | t0001 | g0099 | EAS | JPT | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA19091 | hp1 | a0002 | c0003 | t0001 | g0121 | EAS | JPT | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA19091 | hp2 | a0002 | c0003 | t0001 | g0091 | EAS | JPT | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA19240 | hp1 | a0001 | c0001 | t0005 | g0010 | AFR | YRI | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA19240 | hp2 | a0001 | c0006 | t0005 | g0288 | AFR | YRI | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA20129 | hp1 | a0001 | c0001 | t0008 | g0285 | AFR | ASW | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA20129 | hp2 | a0001 | c0001 | t0005 | g0264 | AFR | ASW | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA20752 | hp1 | a0001 | c0001 | t0003 | g0249 | EUR | TSI | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0179 | EUR | TSI | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA20805 | hp1 | a0001 | c0001 | t0005 | g0303 | EUR | TSI | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0117 | EUR | TSI | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA20905 | hp1 | a0008 | c0013 | t0001 | g0027 | SAS | GIH | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA20905 | hp2 | a0001 | c0001 | t0003 | g0242 | SAS | GIH | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG01123 | hp1 | a0002 | c0003 | t0001 | g0108 | AMR | CLM | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG01123 | hp2 | a0002 | c0002 | t0001 | g0227 | AMR | CLM | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG02109 | hp1 | a0001 | c0001 | t0016 | g0216 | AFR | ACB | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG02109 | hp2 | a0001 | c0001 | t0009 | g0274 | AFR | ACB | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG02559 | hp1 | a0002 | c0002 | t0001 | g0180 | AFR | ACB | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG02559 | hp2 | a0001 | c0001 | t0005 | g0297 | AFR | ACB | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG03471 | hp1 | a0001 | c0001 | t0005 | g0010 | AFR | MSL | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG03471 | hp2 | a0001 | c0001 | t0006 | g0079 | AFR | MSL | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG06807 | hp1 | a0002 | c0002 | t0001 | g0001 | AFR | USA | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | USA | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA20300 | hp1 | a0001 | c0004 | t0006 | g0009 | AFR | USA | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | USA | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA21309 | hp1 | a0001 | c0011 | t0003 | g0043 | AFR | LWK | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| NA21309 | hp2 | a0002 | c0003 | t0001 | g0170 | AFR | LWK | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0174 | REF | REF | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0003 | g0145 | REF | REF | EFHD1_chr2_232628604_232687776 | EFHD1 | chr2 | 232628604 | 232687776 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:232633721 | T | G | 1 | a0004 | 4 | HG00733.hp2 HG00735.hp1 HG01074.hp2 others(1): Show |
missense_variant | MODERATE | c.17T>G | p.Leu6Arg | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/4 | 118/1878 | 17/720 | 6/239 | chr2 | 232633721 | |||
| chr2:232633796 | C | T | 3 | a0003 a0005 a0008 |
13 | HG01433.hp2 HG02129.hp2 HG02258.hp2 others(10): Show |
missense_variant | MODERATE | c.92C>T | p.Ala31Val | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/4 | 193/1878 | 92/720 | 31/239 | chr2 | 232633796 | |||
| chr2:232662866 | G | A | 1 | a0008 | 1 | NA20905.hp1 | missense_variant | MODERATE | c.367G>A | p.Gly123Arg | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 2/4 | 468/1878 | 367/720 | 123/239 | chr2 | 232662866 | |||
| chr2:232662887 | G | A | 1 | a0007 | 1 | NA18957.hp1 | missense_variant | MODERATE | c.388G>A | p.Gly130Ser | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 2/4 | 489/1878 | 388/720 | 130/239 | chr2 | 232662887 | |||
| chr2:232672415 | A | G | 5 | a0002 a0004 a0005 others(2): Show |
149 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(146): Show |
missense_variant | MODERATE | c.557A>G | p.Lys186Arg | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/4 | 658/1878 | 557/720 | 186/239 | chr2 | 232672415 | |||
| chr2:232681702 | G | A | 1 | a0006 | 1 | NA18941.hp1 | missense_variant | MODERATE | c.703G>A | p.Ala235Thr | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 4/4 | 804/1878 | 703/720 | 235/239 | chr2 | 232681702 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:232633725 | G | A | 1 | a0001c0009 | 1 | HG03669.hp2 | synonymous_variant | LOW | c.21G>A | p.Ala7Ala | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/4 | 122/1878 | 21/720 | 7/239 | chr2 | 232633725 | |||
| chr2:232633959 | G | T | 5 | a0001c0004 a0001c0011 a0002c0003 others(2): Show |
139 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(136): Show |
synonymous_variant | LOW | c.255G>T | p.Pro85Pro | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/4 | 356/1878 | 255/720 | 85/239 | chr2 | 232633959 | |||
| chr2:232662898 | C | T | 1 | a0001c0006 | 5 | HG02965.hp1 HG03130.hp2 HG03195.hp2 others(2): Show |
synonymous_variant | LOW | c.399C>T | p.Ser133Ser | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 2/4 | 500/1878 | 399/720 | 133/239 | chr2 | 232662898 | |||
| chr2:232672335 | G | A | 1 | a0001c0011 | 1 | NA21309.hp1 | synonymous_variant | LOW | c.477G>A | p.Ala159Ala | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/4 | 578/1878 | 477/720 | 159/239 | chr2 | 232672335 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:232633608 | T | A | 1 | a0001c0001t0012 | 1 | NA19056.hp1 | 5_prime_UTR_variant | MODIFIER | c.-97T>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/4 | 97 | chr2 | 232633608 | ||||||
| chr2:232633611 | T | C | 1 | a0001c0001t0012 | 1 | NA19056.hp1 | 5_prime_UTR_variant | MODIFIER | c.-94T>C | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/4 | 94 | chr2 | 232633611 | ||||||
| chr2:232633641 | C | CGCCCGCG others(17): Show |
1 | a0001c0001t0012 | 1 | NA19056.hp1 | 5_prime_UTR_variant | MODIFIER | c.-58_-57insGAGTTTGT others(16): Show |
EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/4 | 57 | INFO_REALIGN_3_PRIME | chr2 | 232633641 | |||||
| chr2:232633682 | C | T | 1 | a0001c0001t0023 | 1 | HG02886.hp1 | 5_prime_UTR_variant | MODIFIER | c.-23C>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/4 | 23 | chr2 | 232633682 | ||||||
| chr2:232633689 | C | T | 7 | a0001c0001t0005 a0001c0001t0007 a0001c0001t0008 others(4): Show |
36 | HG00280.hp1 HG00642.hp1 HG01175.hp2 others(33): Show |
5_prime_UTR_variant | MODIFIER | c.-16C>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/4 | 16 | chr2 | 232633689 | ||||||
| chr2:232633690 | C | T | 4 | a0001c0001t0009 a0001c0001t0020 a0001c0001t0021 others(1): Show |
6 | HG02109.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-15C>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/4 | chr2 | 232633690 | |||||||
| chr2:232681854 | G | A | 7 | a0001c0001t0004 a0001c0001t0011 a0001c0001t0012 others(4): Show |
36 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*135G>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 4/4 | 135 | chr2 | 232681854 | ||||||
| chr2:232681870 | C | T | 4 | a0001c0001t0004 a0001c0001t0012 a0001c0001t0020 others(1): Show |
33 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*151C>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 4/4 | 151 | chr2 | 232681870 | ||||||
| chr2:232682036 | C | A | 1 | a0002c0003t0014 | 1 | HG03831.hp2 | 3_prime_UTR_variant | MODIFIER | c.*317C>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 4/4 | 317 | chr2 | 232682036 | ||||||
| chr2:232682060 | T | C | 6 | a0001c0001t0006 a0001c0001t0008 a0001c0001t0021 others(3): Show |
25 | HG01109.hp2 HG01243.hp1 HG01891.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*341T>C | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 4/4 | 341 | chr2 | 232682060 | ||||||
| chr2:232682149 | C | G | 1 | a0002c0003t0019 | 1 | HG03704.hp2 | 3_prime_UTR_variant | MODIFIER | c.*430C>G | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 4/4 | 430 | chr2 | 232682149 | ||||||
| chr2:232682275 | T | C | 39 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(36): Show |
314 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(311): Show |
3_prime_UTR_variant | MODIFIER | c.*556T>C | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 4/4 | 556 | chr2 | 232682275 | ||||||
| chr2:232682349 | C | A | 1 | a0002c0002t0015 | 1 | NA19062.hp1 | 3_prime_UTR_variant | MODIFIER | c.*630C>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 4/4 | 630 | chr2 | 232682349 | ||||||
| chr2:232682368 | CTTGCTCC others(20): Show |
C | 1 | a0001c0001t0016 | 1 | HG02109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*650_*676delTTGCTC others(21): Show |
EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 4/4 | 650 | chr2 | 232682368 | ||||||
| chr2:232682418 | C | T | 2 | a0001c0001t0011 a0003c0005t0011 |
2 | HG02723.hp1 HG03516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*699C>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 4/4 | 699 | chr2 | 232682418 | ||||||
| chr2:232682518 | C | T | 2 | a0001c0001t0016 a0002c0003t0018 |
2 | HG02083.hp1 HG02109.hp1 |
3_prime_UTR_variant | MODIFIER | c.*799C>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 4/4 | 799 | chr2 | 232682518 | ||||||
| chr2:232682656 | C | A | 4 | a0001c0001t0002 a0001c0001t0010 a0001c0004t0002 others(1): Show |
58 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(55): Show |
3_prime_UTR_variant | MODIFIER | c.*937C>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 4/4 | 937 | chr2 | 232682656 | ||||||
| chr2:232682698 | T | G | 1 | a0002c0002t0017 | 1 | HG01975.hp1 | 3_prime_UTR_variant | MODIFIER | c.*979T>G | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 4/4 | 979 | chr2 | 232682698 | ||||||
| chr2:232682710 | C | A | 1 | a0001c0001t0016 | 1 | HG02109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*991C>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 4/4 | 991 | chr2 | 232682710 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:232634080 | G | T | 108 | a0001c0001t0001g0265 a0001c0001t0001g0308 a0001c0001t0001g0315 others(105): Show |
112 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.302+74G>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232634080 | |||||||
| chr2:232634121 | C | T | 1 | a0002c0002t0022g0263 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.302+115C>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232634121 | |||||||
| chr2:232634132 | A | G | 2 | a0001c0004t0002g0262 a0001c0004t0006g0009 |
3 | HG03098.hp2 HG03225.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.302+126A>G | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232634132 | |||||||
| chr2:232634171 | G | A | 1 | a0001c0001t0005g0264 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.302+165G>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232634171 | |||||||
| chr2:232634228 | G | T | 107 | a0001c0001t0001g0308 a0001c0001t0001g0315 a0001c0001t0001g0356 others(104): Show |
111 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.302+222G>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232634228 | |||||||
| chr2:232634280 | G | C | 3 | a0001c0001t0001g0012 a0001c0001t0002g0013 a0001c0001t0003g0014 |
3 | HG00099.hp2 HG01106.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.302+274G>C | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232634280 | |||||||
| chr2:232634317 | G | T | 2 | a0002c0003t0001g0260 a0002c0003t0001g0261 |
2 | HG00642.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.302+311G>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232634317 | |||||||
| chr2:232634374 | G | C | 1 | a0003c0005t0002g0015 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.302+368G>C | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232634374 | |||||||
| chr2:232634391 | C | A | 1 | a0001c0001t0001g0265 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.302+385C>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232634391 | |||||||
| chr2:232634434 | C | G | 1 | a0003c0005t0006g0259 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.302+428C>G | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232634434 | |||||||
| chr2:232634870 | G | A | 1 | a0001c0004t0002g0016 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.302+864G>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232634870 | |||||||
| chr2:232634994 | G | GGCGCTGC others(13): Show |
31 | a0001c0001t0002g0246 a0001c0001t0002g0252 a0001c0001t0002g0253 others(28): Show |
33 | HG00099.hp2 HG00140.hp1 HG00609.hp2 others(30): Show |
intron_variant | MODIFIER | c.302+989_302+1008du others(21): Show |
EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 232634994 | ||||||
| chr2:232635080 | G | A | 99 | a0001c0001t0001g0019 a0001c0001t0001g0024 a0001c0001t0001g0033 others(96): Show |
104 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.302+1074G>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232635080 | |||||||
| chr2:232635182 | T | A | 3 | a0001c0004t0006g0041 a0001c0004t0006g0042 a0001c0011t0003g0043 |
3 | NA18906.hp2 NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.302+1176T>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232635182 | |||||||
| chr2:232635385 | G | A | 3 | a0001c0001t0003g0266 a0001c0001t0003g0268 a0001c0006t0001g0267 |
3 | HG02965.hp1 HG02976.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.302+1379G>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232635385 | |||||||
| chr2:232635515 | G | T | 2 | a0001c0001t0003g0268 a0001c0006t0001g0267 |
2 | HG02965.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.302+1509G>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232635515 | |||||||
| chr2:232635527 | C | T | 1 | a0001c0004t0004g0230 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.302+1521C>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232635527 | |||||||
| chr2:232635615 | T | G | 176 | a0001c0001t0001g0019 a0001c0001t0001g0024 a0001c0001t0001g0033 others(173): Show |
181 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.302+1609T>G | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232635615 | |||||||
| chr2:232635721 | A | G | 4 | a0001c0001t0003g0256 a0002c0002t0001g0254 a0002c0002t0001g0255 others(1): Show |
4 | HG00140.hp1 HG01258.hp1 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.302+1715A>G | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232635721 | |||||||
| chr2:232635824 | GA | G | 30 | a0001c0001t0005g0010 a0001c0001t0005g0264 a0001c0001t0005g0281 others(27): Show |
33 | HG00280.hp1 HG00642.hp1 HG01175.hp2 others(30): Show |
intron_variant | MODIFIER | c.302+1829delA | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 232635824 | ||||||
| chr2:232635957 | C | T | 1 | a0002c0002t0001g0229 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.302+1951C>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232635957 | |||||||
| chr2:232635962 | A | C | 1 | a0001c0001t0003g0228 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.302+1956A>C | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232635962 | |||||||
| chr2:232635973 | G | A | 2 | a0002c0003t0001g0066 a0002c0003t0001g0067 |
2 | HG01346.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.302+1967G>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232635973 | |||||||
| chr2:232636456 | G | C | 1 | a0003c0005t0002g0015 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.302+2450G>C | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232636456 | |||||||
| chr2:232636528 | G | A | 1 | a0001c0001t0003g0307 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.302+2522G>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232636528 | |||||||
| chr2:232636737 | C | T | 1 | a0001c0001t0002g0253 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.302+2731C>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232636737 | |||||||
| chr2:232636816 | C | T | 1 | a0001c0001t0002g0252 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.302+2810C>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232636816 | |||||||
| chr2:232636818 | G | A | 1 | a0001c0001t0006g0269 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.302+2812G>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232636818 | |||||||
| chr2:232636954 | G | T | 79 | a0001c0001t0001g0308 a0001c0001t0001g0315 a0001c0001t0001g0356 others(76): Show |
79 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.302+2948G>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232636954 | |||||||
| chr2:232637156 | A | G | 11 | a0001c0001t0001g0033 a0001c0001t0001g0036 a0001c0001t0003g0032 others(8): Show |
11 | HG01109.hp2 HG02055.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.302+3150A>G | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232637156 | |||||||
| chr2:232637157 | C | T | 22 | a0001c0001t0001g0024 a0001c0001t0001g0033 a0001c0001t0001g0036 others(19): Show |
22 | HG01099.hp1 HG01109.hp2 HG01433.hp2 others(19): Show |
intron_variant | MODIFIER | c.302+3151C>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232637157 | |||||||
| chr2:232637274 | C | T | 6 | a0001c0001t0006g0269 a0001c0001t0006g0277 a0001c0001t0006g0278 others(3): Show |
6 | HG02630.hp2 HG02647.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.302+3268C>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232637274 | |||||||
| chr2:232637343 | C | CT | 39 | a0001c0001t0001g0356 a0001c0001t0002g0246 a0001c0001t0002g0252 others(36): Show |
41 | HG00099.hp2 HG00140.hp1 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.302+3355dupT | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 232637343 | ||||||
| chr2:232637343 | C | CTT | 11 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(8): Show |
11 | HG00544.hp2 HG01167.hp1 HG01261.hp1 others(8): Show |
intron_variant | MODIFIER | c.302+3354_302+3355d others(4): Show |
EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 232637343 | ||||||
| chr2:232637343 | CT | C | 5 | a0001c0001t0003g0270 a0002c0003t0001g0003 a0002c0003t0001g0068 others(2): Show |
6 | HG02155.hp2 HG02897.hp1 NA18969.hp1 others(3): Show |
intron_variant | MODIFIER | c.302+3355delT | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 232637343 | ||||||
| chr2:232637389 | G | T | 1 | a0001c0004t0003g0224 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.302+3383G>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232637389 | |||||||
| chr2:232637469 | G | A | 7 | a0001c0004t0003g0071 a0002c0003t0001g0070 a0002c0003t0001g0072 others(4): Show |
7 | HG00438.hp2 NA18747.hp1 NA18995.hp1 others(4): Show |
intron_variant | MODIFIER | c.302+3463G>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232637469 | |||||||
| chr2:232637489 | G | A | 1 | a0001c0001t0001g0077 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.302+3483G>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232637489 | |||||||
| chr2:232637634 | G | A | 82 | a0001c0001t0001g0308 a0001c0001t0001g0315 a0001c0001t0001g0356 others(79): Show |
82 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.302+3628G>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232637634 | |||||||
| chr2:232637719 | A | G | 13 | a0001c0001t0003g0270 a0001c0001t0003g0275 a0001c0001t0006g0269 others(10): Show |
13 | HG02109.hp2 HG02622.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.302+3713A>G | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232637719 | |||||||
| chr2:232637954 | A | G | 4 | a0001c0001t0003g0256 a0002c0002t0001g0254 a0002c0002t0001g0255 others(1): Show |
4 | HG00140.hp1 HG01258.hp1 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.302+3948A>G | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232637954 | |||||||
| chr2:232638097 | T | C | 1 | a0001c0001t0006g0079 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.302+4091T>C | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232638097 | |||||||
| chr2:232638274 | A | G | 137 | a0001c0001t0001g0012 a0001c0001t0001g0194 a0001c0001t0001g0265 others(134): Show |
141 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.302+4268A>G | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232638274 | |||||||
| chr2:232638303 | G | A | 1 | a0002c0002t0001g0254 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.302+4297G>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232638303 | |||||||
| chr2:232638305 | C | T | 2 | a0001c0001t0001g0356 a0001c0001t0003g0357 |
2 | HG02145.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.302+4299C>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232638305 | |||||||
| chr2:232638331 | G | T | 17 | a0001c0001t0005g0264 a0001c0001t0005g0286 a0001c0001t0005g0293 others(14): Show |
19 | HG01884.hp1 HG01891.hp1 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.302+4325G>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232638331 | |||||||
| chr2:232638384 | G | A | 4 | a0001c0001t0001g0308 a0001c0001t0001g0356 a0001c0001t0003g0357 others(1): Show |
4 | HG02145.hp1 HG02572.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.302+4378G>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232638384 | |||||||
| chr2:232638416 | G | A | 1 | a0001c0001t0001g0356 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.302+4410G>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232638416 | |||||||
| chr2:232638546 | C | T | 1 | a0002c0003t0001g0076 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.302+4540C>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232638546 | |||||||
| chr2:232638856 | G | T | 9 | a0001c0001t0001g0077 a0001c0001t0002g0013 a0001c0001t0002g0179 others(6): Show |
9 | HG00280.hp2 HG01106.hp1 HG01261.hp2 others(6): Show |
intron_variant | MODIFIER | c.302+4850G>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232638856 | |||||||
| chr2:232638917 | A | G | 1 | a0001c0001t0010g0298 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.302+4911A>G | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232638917 | |||||||
| chr2:232638927 | A | G | 3 | a0001c0001t0005g0297 a0001c0001t0007g0296 a0001c0001t0010g0298 |
3 | HG02559.hp2 HG02572.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.302+4921A>G | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232638927 | |||||||
| chr2:232638968 | G | A | 6 | a0001c0004t0001g0057 a0002c0003t0001g0080 a0003c0005t0001g0021 others(3): Show |
6 | HG00673.hp2 HG01099.hp1 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.302+4962G>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232638968 | |||||||
| chr2:232639056 | T | C | 1 | a0001c0001t0003g0228 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.302+5050T>C | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232639056 | |||||||
| chr2:232639152 | C | T | 1 | a0001c0001t0001g0019 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.302+5146C>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232639152 | |||||||
| chr2:232639158 | G | A | 4 | a0001c0001t0005g0010 a0001c0001t0005g0281 a0001c0001t0005g0282 others(1): Show |
5 | HG03453.hp1 HG03471.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.302+5152G>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232639158 | |||||||
| chr2:232639194 | A | C | 1 | a0002c0002t0001g0173 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.302+5188A>C | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232639194 | |||||||
| chr2:232639279 | G | A | 140 | a0001c0001t0001g0019 a0001c0001t0001g0024 a0001c0001t0001g0033 others(137): Show |
147 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(144): Show |
intron_variant | MODIFIER | c.302+5273G>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232639279 | |||||||
| chr2:232639366 | T | C | 1 | a0002c0002t0001g0318 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.302+5360T>C | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232639366 | |||||||
| chr2:232639452 | G | A | 2 | a0001c0004t0003g0071 a0002c0003t0001g0070 |
2 | NA18995.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.302+5446G>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232639452 | |||||||
| chr2:232639636 | T | C | 138 | a0001c0001t0001g0019 a0001c0001t0001g0024 a0001c0001t0001g0033 others(135): Show |
146 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(143): Show |
intron_variant | MODIFIER | c.302+5630T>C | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232639636 | |||||||
| chr2:232639903 | C | T | 6 | a0001c0001t0005g0286 a0001c0001t0008g0285 a0001c0001t0008g0287 others(3): Show |
6 | HG01891.hp1 HG02257.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.302+5897C>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232639903 | |||||||
| chr2:232640018 | C | A | 1 | a0001c0001t0004g0320 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.302+6012C>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232640018 | |||||||
| chr2:232640437 | G | A | 8 | a0001c0001t0001g0033 a0001c0001t0003g0032 a0001c0001t0004g0031 others(5): Show |
8 | HG01243.hp1 HG02055.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.302+6431G>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232640437 | |||||||
| chr2:232640551 | A | G | 1 | a0002c0003t0001g0099 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.302+6545A>G | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232640551 | |||||||
| chr2:232640567 | T | A | 142 | a0001c0001t0001g0019 a0001c0001t0001g0024 a0001c0001t0001g0033 others(139): Show |
150 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(147): Show |
intron_variant | MODIFIER | c.302+6561T>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232640567 | |||||||
| chr2:232640680 | C | T | 3 | a0001c0001t0001g0024 a0001c0001t0006g0025 a0001c0001t0006g0026 |
3 | HG02280.hp1 HG02886.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.302+6674C>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232640680 | |||||||
| chr2:232640693 | A | G | 11 | a0001c0001t0001g0033 a0001c0001t0003g0032 a0001c0001t0004g0031 others(8): Show |
12 | HG01243.hp1 HG02055.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.302+6687A>G | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232640693 | |||||||
| chr2:232640704 | A | C | 1 | a0002c0002t0001g0363 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.302+6698A>C | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232640704 | |||||||
| chr2:232640812 | C | T | 28 | a0001c0001t0002g0246 a0001c0001t0002g0252 a0001c0001t0002g0253 others(25): Show |
30 | HG00099.hp2 HG00140.hp1 HG00609.hp2 others(27): Show |
intron_variant | MODIFIER | c.302+6806C>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232640812 | |||||||
| chr2:232641136 | G | A | 1 | a0001c0004t0003g0183 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.302+7130G>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232641136 | |||||||
| chr2:232641176 | G | A | 3 | a0001c0004t0004g0104 a0001c0004t0004g0105 a0001c0004t0004g0230 |
3 | HG00408.hp2 HG02523.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.302+7170G>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232641176 | |||||||
| chr2:232641189 | C | T | 1 | a0001c0001t0002g0355 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.302+7183C>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232641189 | |||||||
| chr2:232641198 | T | C | 144 | a0001c0001t0001g0019 a0001c0001t0001g0024 a0001c0001t0001g0033 others(141): Show |
152 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(149): Show |
intron_variant | MODIFIER | c.302+7192T>C | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232641198 | |||||||
| chr2:232641336 | A | G | 14 | a0001c0001t0001g0172 a0001c0001t0004g0319 a0001c0001t0004g0352 others(11): Show |
14 | HG00323.hp1 HG03041.hp1 HG03139.hp1 others(11): Show |
intron_variant | MODIFIER | c.302+7330A>G | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232641336 | |||||||
| chr2:232641557 | T | A | 3 | a0001c0001t0001g0024 a0001c0001t0006g0025 a0001c0001t0006g0026 |
3 | HG02280.hp1 HG02886.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.302+7551T>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232641557 | |||||||
| chr2:232641560 | G | A | 2 | a0001c0001t0009g0273 a0001c0001t0009g0274 |
2 | HG02109.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.302+7554G>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232641560 | |||||||
| chr2:232641589 | G | A | 138 | a0001c0001t0001g0019 a0001c0001t0001g0024 a0001c0001t0001g0033 others(135): Show |
146 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(143): Show |
intron_variant | MODIFIER | c.302+7583G>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232641589 | |||||||
| chr2:232641608 | T | C | 1 | a0001c0009t0005g0299 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.302+7602T>C | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232641608 | |||||||
| chr2:232641757 | G | A | 6 | a0001c0001t0005g0286 a0001c0001t0008g0285 a0001c0001t0008g0287 others(3): Show |
6 | HG01891.hp1 HG02257.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.302+7751G>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232641757 | |||||||
| chr2:232641779 | A | C | 1 | a0001c0001t0010g0306 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.302+7773A>C | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232641779 | |||||||
| chr2:232641925 | G | A | 2 | a0001c0001t0001g0036 a0001c0001t0003g0037 |
2 | HG02145.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.302+7919G>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232641925 | |||||||
| chr2:232641958 | G | A | 11 | a0001c0001t0004g0319 a0001c0001t0004g0352 a0001c0001t0004g0353 others(8): Show |
11 | HG00323.hp1 NA18942.hp2 NA18972.hp2 others(8): Show |
intron_variant | MODIFIER | c.302+7952G>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232641958 | |||||||
| chr2:232641960 | G | A | 2 | a0002c0002t0005g0284 a0003c0005t0006g0259 |
2 | HG02809.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.302+7954G>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232641960 | |||||||
| chr2:232641978 | G | GC | 12 | a0001c0004t0003g0082 a0001c0004t0003g0083 a0001c0004t0003g0183 others(9): Show |
12 | HG02135.hp2 NA18939.hp2 NA18944.hp1 others(9): Show |
intron_variant | MODIFIER | c.302+7973dupC | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 232641978 | ||||||
| chr2:232641992 | C | T | 174 | a0001c0001t0001g0012 a0001c0001t0001g0019 a0001c0001t0001g0024 others(171): Show |
182 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(179): Show |
intron_variant | MODIFIER | c.302+7986C>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232641992 | |||||||
| chr2:232642171 | T | G | 2 | a0001c0001t0004g0352 a0001c0001t0012g0351 |
2 | NA18981.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.302+8165T>G | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232642171 | |||||||
| chr2:232642373 | C | CA | 56 | a0001c0001t0001g0012 a0001c0001t0001g0036 a0001c0001t0001g0048 others(53): Show |
56 | HG00280.hp1 HG00323.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.302+8391dupA | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 232642373 | ||||||
| chr2:232642373 | C | CAA | 8 | a0001c0001t0001g0172 a0001c0001t0001g0356 a0001c0001t0003g0357 others(5): Show |
8 | HG02145.hp1 HG02257.hp1 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.302+8390_302+8391d others(4): Show |
EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 232642373 | ||||||
| chr2:232642373 | CA | C | 120 | a0001c0001t0001g0265 a0001c0001t0001g0315 a0001c0001t0002g0200 others(117): Show |
128 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(125): Show |
intron_variant | MODIFIER | c.302+8391delA | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 232642373 | ||||||
| chr2:232642373 | CAAAAAAA others(5): Show |
C | 4 | a0001c0001t0001g0033 a0001c0001t0003g0032 a0001c0001t0004g0031 others(1): Show |
4 | HG02055.hp1 HG02615.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.302+8380_302+8391d others(14): Show |
EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 232642373 | ||||||
| chr2:232642447 | G | A | 2 | a0001c0001t0001g0019 a0001c0001t0001g0265 |
2 | HG03540.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.302+8441G>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232642447 | |||||||
| chr2:232642456 | G | A | 1 | a0002c0002t0001g0233 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.302+8450G>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232642456 | |||||||
| chr2:232642551 | G | A | 135 | a0001c0001t0001g0024 a0001c0001t0001g0033 a0001c0001t0001g0194 others(132): Show |
143 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(140): Show |
intron_variant | MODIFIER | c.302+8545G>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232642551 | |||||||
| chr2:232642675 | T | G | 2 | a0001c0001t0002g0321 a0003c0005t0002g0060 |
2 | HG03654.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.302+8669T>G | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232642675 | |||||||
| chr2:232642738 | C | T | 1 | a0002c0002t0001g0046 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.302+8732C>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232642738 | |||||||
| chr2:232642788 | A | G | 1 | a0002c0002t0001g0255 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.302+8782A>G | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232642788 | |||||||
| chr2:232642896 | C | G | 1 | a0001c0001t0006g0026 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.302+8890C>G | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232642896 | |||||||
| chr2:232642973 | C | T | 18 | a0001c0001t0004g0319 a0001c0001t0004g0352 a0001c0001t0004g0353 others(15): Show |
18 | HG00323.hp1 HG01891.hp1 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.302+8967C>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232642973 | |||||||
| chr2:232643003 | G | A | 17 | a0001c0001t0001g0019 a0001c0001t0001g0033 a0001c0001t0001g0265 others(14): Show |
17 | HG01243.hp1 HG01891.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.302+8997G>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232643003 | |||||||
| chr2:232643040 | G | A | 1 | a0002c0002t0001g0173 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.302+9034G>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232643040 | |||||||
| chr2:232643100 | G | C | 5 | a0001c0001t0005g0364 a0001c0006t0001g0034 a0001c0006t0001g0267 others(2): Show |
5 | HG01891.hp2 HG02965.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.302+9094G>C | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232643100 | |||||||
| chr2:232643216 | AT | A | 4 | a0001c0001t0002g0117 a0001c0001t0002g0118 a0001c0001t0002g0258 others(1): Show |
4 | HG01433.hp1 HG01516.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.302+9211delT | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232643216 | |||||||
| chr2:232643294 | T | A | 6 | a0001c0001t0003g0228 a0001c0001t0003g0266 a0001c0001t0003g0268 others(3): Show |
6 | HG02572.hp1 HG02976.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.302+9288T>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232643294 | |||||||
| chr2:232643409 | T | TA | 10 | a0001c0001t0001g0052 a0001c0004t0001g0221 a0002c0002t0001g0053 others(7): Show |
10 | HG01167.hp1 HG01934.hp2 HG02293.hp2 others(7): Show |
intron_variant | MODIFIER | c.302+9404dupA | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 232643409 | ||||||
| chr2:232643431 | A | G | 1 | a0001c0001t0001g0012 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.302+9425A>G | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232643431 | |||||||
| chr2:232643523 | C | T | 22 | a0001c0001t0001g0019 a0001c0001t0001g0033 a0001c0001t0001g0265 others(19): Show |
22 | HG01109.hp2 HG01243.hp1 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.302+9517C>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232643523 | |||||||
| chr2:232643829 | C | T | 8 | a0001c0001t0003g0307 a0001c0001t0005g0364 a0001c0001t0016g0216 others(5): Show |
8 | HG01891.hp2 HG02109.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.302+9823C>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232643829 | |||||||
| chr2:232643840 | G | A | 1 | a0001c0001t0006g0361 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.302+9834G>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232643840 | |||||||
| chr2:232643921 | C | A | 5 | a0001c0001t0006g0035 a0001c0001t0006g0097 a0001c0001t0006g0098 others(2): Show |
5 | HG01109.hp2 HG02258.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.302+9915C>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232643921 | |||||||
| chr2:232643934 | G | A | 1 | a0002c0002t0001g0106 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.302+9928G>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232643934 | |||||||
| chr2:232643967 | T | C | 186 | a0001c0001t0001g0012 a0001c0001t0001g0019 a0001c0001t0001g0024 others(183): Show |
194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.302+9961T>C | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232643967 | |||||||
| chr2:232644012 | T | C | 3 | a0001c0001t0004g0352 a0001c0001t0004g0353 a0001c0001t0012g0351 |
3 | NA18981.hp1 NA19056.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.302+10006T>C | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232644012 | |||||||
| chr2:232644106 | C | A | 39 | a0001c0001t0002g0222 a0001c0001t0002g0322 a0001c0001t0002g0323 others(36): Show |
39 | HG00423.hp1 HG00621.hp2 HG01256.hp1 others(36): Show |
intron_variant | MODIFIER | c.302+10100C>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232644106 | |||||||
| chr2:232644196 | GCCTCAC | G | 6 | a0001c0001t0005g0286 a0001c0001t0008g0285 a0001c0001t0008g0287 others(3): Show |
6 | HG01891.hp1 HG02257.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.302+10195_302+1020 others(10): Show |
EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 232644196 | ||||||
| chr2:232644301 | G | A | 3 | a0001c0001t0001g0024 a0001c0001t0006g0025 a0001c0001t0006g0026 |
3 | HG02280.hp1 HG02886.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.302+10295G>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232644301 | |||||||
| chr2:232644316 | T | G | 1 | a0001c0004t0002g0128 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.302+10310T>G | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232644316 | |||||||
| chr2:232644319 | C | T | 10 | a0001c0001t0001g0019 a0001c0001t0001g0033 a0001c0001t0001g0265 others(7): Show |
10 | HG01243.hp1 HG02055.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.302+10313C>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232644319 | |||||||
| chr2:232644371 | G | C | 1 | a0002c0002t0001g0173 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.302+10365G>C | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232644371 | |||||||
| chr2:232644418 | A | G | 12 | a0001c0004t0003g0082 a0001c0004t0003g0083 a0001c0004t0003g0183 others(9): Show |
12 | HG02135.hp2 NA18939.hp2 NA18944.hp1 others(9): Show |
intron_variant | MODIFIER | c.302+10412A>G | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232644418 | |||||||
| chr2:232644501 | T | C | 1 | a0002c0002t0001g0195 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.302+10495T>C | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232644501 | |||||||
| chr2:232644511 | C | A | 1 | a0001c0006t0005g0365 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.302+10505C>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232644511 | |||||||
| chr2:232644513 | A | T | 2 | a0001c0001t0009g0273 a0001c0001t0009g0274 |
2 | HG02109.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.302+10507A>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232644513 | |||||||
| chr2:232644524 | T | A | 6 | a0002c0003t0001g0107 a0002c0003t0001g0108 a0002c0003t0001g0109 others(3): Show |
6 | HG00642.hp2 HG01123.hp1 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.302+10518T>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232644524 | |||||||
| chr2:232644575 | C | T | 11 | a0001c0001t0001g0012 a0001c0001t0001g0036 a0001c0001t0003g0037 others(8): Show |
11 | HG01099.hp1 HG01106.hp2 HG01433.hp2 others(8): Show |
intron_variant | MODIFIER | c.302+10569C>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232644575 | |||||||
| chr2:232644707 | C | T | 10 | a0001c0001t0001g0019 a0001c0001t0001g0033 a0001c0001t0001g0265 others(7): Show |
10 | HG01243.hp1 HG02055.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.302+10701C>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232644707 | |||||||
| chr2:232644791 | C | T | 1 | a0002c0002t0001g0233 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.302+10785C>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232644791 | |||||||
| chr2:232644794 | A | AT | 23 | a0001c0001t0001g0012 a0001c0001t0001g0036 a0001c0001t0003g0037 others(20): Show |
23 | HG00140.hp1 HG00408.hp1 HG01099.hp1 others(20): Show |
intron_variant | MODIFIER | c.302+10808dupT | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 232644794 | ||||||
| chr2:232644794 | AT | A | 28 | a0001c0001t0001g0019 a0001c0001t0001g0172 a0001c0001t0001g0265 others(25): Show |
29 | HG00621.hp1 HG02155.hp2 HG02647.hp2 others(26): Show |
intron_variant | MODIFIER | c.302+10808delT | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 232644794 | ||||||
| chr2:232644794 | ATTT | A | 8 | a0001c0001t0001g0033 a0001c0001t0003g0032 a0001c0001t0004g0031 others(5): Show |
8 | HG01243.hp1 HG02055.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.302+10806_302+1080 others(7): Show |
EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 232644794 | ||||||
| chr2:232644814 | T | A | 5 | a0001c0001t0006g0035 a0001c0001t0006g0097 a0001c0001t0006g0098 others(2): Show |
5 | HG01109.hp2 HG02258.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.302+10808T>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232644814 | |||||||
| chr2:232644922 | G | A | 6 | a0001c0001t0005g0286 a0001c0001t0008g0285 a0001c0001t0008g0287 others(3): Show |
6 | HG01891.hp1 HG02257.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.302+10916G>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232644922 | |||||||
| chr2:232644942 | A | AT | 27 | a0001c0001t0001g0012 a0001c0001t0001g0033 a0001c0001t0002g0355 others(24): Show |
28 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(25): Show |
intron_variant | MODIFIER | c.302+10957dupT | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 232644942 | ||||||
| chr2:232644942 | AT | A | 31 | a0001c0001t0002g0013 a0001c0001t0002g0349 a0001c0001t0002g0367 others(28): Show |
31 | HG00099.hp2 HG01070.hp2 HG01496.hp2 others(28): Show |
intron_variant | MODIFIER | c.302+10957delT | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 232644942 | ||||||
| chr2:232644942 | ATTTTTTT | A | 12 | a0001c0001t0004g0319 a0001c0001t0004g0352 a0001c0001t0004g0353 others(9): Show |
12 | HG00323.hp1 NA18942.hp2 NA18951.hp1 others(9): Show |
intron_variant | MODIFIER | c.302+10951_302+1095 others(11): Show |
EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 232644942 | ||||||
| chr2:232644981 | A | G | 2 | a0002c0002t0005g0284 a0003c0005t0006g0259 |
2 | HG02809.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.302+10975A>G | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232644981 | |||||||
| chr2:232645031 | T | G | 1 | a0002c0003t0001g0066 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.302+11025T>G | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232645031 | |||||||
| chr2:232645051 | C | A | 189 | a0001c0001t0001g0012 a0001c0001t0001g0019 a0001c0001t0001g0024 others(186): Show |
197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.302+11045C>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232645051 | |||||||
| chr2:232645081 | C | G | 208 | a0001c0001t0001g0012 a0001c0001t0001g0019 a0001c0001t0001g0024 others(205): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.302+11075C>G | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232645081 | |||||||
| chr2:232645141 | T | C | 182 | a0001c0001t0001g0012 a0001c0001t0001g0024 a0001c0001t0001g0036 others(179): Show |
190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.302+11135T>C | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232645141 | |||||||
| chr2:232645142 | G | A | 13 | a0001c0001t0001g0172 a0001c0001t0004g0319 a0001c0001t0004g0352 others(10): Show |
13 | HG00323.hp1 HG03041.hp1 HG03139.hp1 others(10): Show |
intron_variant | MODIFIER | c.302+11136G>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232645142 | |||||||
| chr2:232645250 | C | T | 5 | a0001c0001t0006g0035 a0001c0001t0006g0097 a0001c0001t0006g0098 others(2): Show |
5 | HG01109.hp2 HG02258.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.302+11244C>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232645250 | |||||||
| chr2:232645268 | C | T | 6 | a0001c0001t0003g0228 a0001c0001t0003g0266 a0001c0001t0003g0268 others(3): Show |
6 | HG02572.hp1 HG02976.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.302+11262C>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232645268 | |||||||
| chr2:232645301 | C | T | 198 | a0001c0001t0001g0012 a0001c0001t0001g0019 a0001c0001t0001g0024 others(195): Show |
206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.302+11295C>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232645301 | |||||||
| chr2:232645333 | C | G | 1 | a0003c0005t0002g0015 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.302+11327C>G | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232645333 | |||||||
| chr2:232645358 | G | C | 1 | a0001c0001t0007g0290 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.302+11352G>C | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232645358 | |||||||
| chr2:232645360 | C | A | 14 | a0001c0001t0001g0172 a0001c0001t0004g0319 a0001c0001t0004g0352 others(11): Show |
14 | HG00323.hp1 HG03041.hp1 HG03139.hp1 others(11): Show |
intron_variant | MODIFIER | c.302+11354C>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232645360 | |||||||
| chr2:232645556 | C | T | 1 | a0002c0003t0001g0161 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.302+11550C>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232645556 | |||||||
| chr2:232645762 | A | G | 3 | a0002c0002t0001g0310 a0002c0002t0001g0312 a0002c0002t0017g0311 |
3 | HG01975.hp1 NA18948.hp2 NA18952.hp1 |
intron_variant | MODIFIER | c.302+11756A>G | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232645762 | |||||||
| chr2:232645912 | A | G | 120 | a0001c0001t0001g0194 a0001c0001t0001g0315 a0001c0001t0002g0200 others(117): Show |
128 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(125): Show |
intron_variant | MODIFIER | c.302+11906A>G | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232645912 | |||||||
| chr2:232646052 | C | T | 1 | a0001c0001t0001g0012 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.302+12046C>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232646052 | |||||||
| chr2:232646094 | G | A | 1 | a0002c0003t0019g0129 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.302+12088G>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232646094 | |||||||
| chr2:232646196 | C | T | 29 | a0001c0001t0002g0246 a0001c0001t0002g0252 a0001c0001t0002g0253 others(26): Show |
31 | HG00099.hp2 HG00140.hp1 HG00609.hp2 others(28): Show |
intron_variant | MODIFIER | c.302+12190C>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232646196 | |||||||
| chr2:232646197 | G | A | 1 | a0001c0004t0003g0082 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.302+12191G>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232646197 | |||||||
| chr2:232646201 | G | C | 4 | a0001c0001t0001g0033 a0001c0001t0003g0032 a0001c0001t0004g0031 others(1): Show |
4 | HG02055.hp1 HG02615.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.302+12195G>C | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232646201 | |||||||
| chr2:232646269 | T | C | 43 | a0001c0001t0001g0024 a0001c0001t0002g0246 a0001c0001t0002g0252 others(40): Show |
45 | HG00099.hp2 HG00140.hp1 HG00609.hp2 others(42): Show |
intron_variant | MODIFIER | c.302+12263T>C | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232646269 | |||||||
| chr2:232646293 | T | C | 1 | a0001c0001t0002g0323 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.302+12287T>C | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232646293 | |||||||
| chr2:232646308 | C | A | 1 | a0001c0001t0006g0030 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.302+12302C>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232646308 | |||||||
| chr2:232646391 | C | T | 1 | a0001c0001t0001g0265 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.302+12385C>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232646391 | |||||||
| chr2:232646429 | T | G | 5 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(2): Show |
5 | HG00544.hp2 HG02300.hp1 NA18951.hp2 others(2): Show |
intron_variant | MODIFIER | c.302+12423T>G | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232646429 | |||||||
| chr2:232646436 | C | CT | 72 | a0001c0001t0002g0200 a0001c0001t0002g0246 a0001c0001t0002g0252 others(69): Show |
74 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.302+12456dupT | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 232646436 | ||||||
| chr2:232646436 | C | CTT | 67 | a0001c0001t0001g0194 a0001c0001t0001g0315 a0001c0001t0002g0203 others(64): Show |
73 | HG00099.hp1 HG00558.hp2 HG00597.hp2 others(70): Show |
intron_variant | MODIFIER | c.302+12455_302+1245 others(6): Show |
EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 232646436 | ||||||
| chr2:232646436 | CT | C | 49 | a0001c0001t0001g0012 a0001c0001t0001g0019 a0001c0001t0001g0024 others(46): Show |
49 | HG00280.hp1 HG00558.hp1 HG00642.hp1 others(46): Show |
intron_variant | MODIFIER | c.302+12456delT | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 232646436 | ||||||
| chr2:232646436 | CTT | C | 9 | a0001c0001t0001g0265 a0001c0001t0006g0277 a0001c0001t0008g0285 others(6): Show |
9 | HG01891.hp1 HG02257.hp2 HG02735.hp1 others(6): Show |
intron_variant | MODIFIER | c.302+12455_302+1245 others(6): Show |
EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 232646436 | ||||||
| chr2:232646436 | CTTT | C | 6 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(3): Show |
6 | HG00544.hp2 HG02300.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.302+12454_302+1245 others(7): Show |
EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 232646436 | ||||||
| chr2:232646436 | CTTTTTTT others(4): Show |
C | 2 | a0001c0001t0005g0300 a0001c0009t0005g0299 |
2 | HG03239.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.302+12446_302+1245 others(15): Show |
EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 232646436 | ||||||
| chr2:232646479 | CTG | C | 29 | a0001c0001t0002g0246 a0001c0001t0002g0252 a0001c0001t0002g0253 others(26): Show |
31 | HG00099.hp2 HG00140.hp1 HG00609.hp2 others(28): Show |
intron_variant | MODIFIER | c.302+12475_302+1247 others(6): Show |
EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 232646479 | ||||||
| chr2:232646485 | C | T | 1 | a0001c0004t0004g0171 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.302+12479C>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232646485 | |||||||
| chr2:232646717 | G | A | 17 | a0001c0001t0001g0077 a0001c0001t0002g0013 a0001c0001t0002g0117 others(14): Show |
17 | HG00140.hp2 HG00280.hp2 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.302+12711G>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232646717 | |||||||
| chr2:232647061 | C | G | 6 | a0001c0001t0001g0033 a0001c0001t0003g0032 a0001c0001t0004g0031 others(3): Show |
6 | HG01243.hp1 HG02055.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.302+13055C>G | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232647061 | |||||||
| chr2:232647109 | A | G | 1 | a0002c0002t0001g0132 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.302+13103A>G | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232647109 | |||||||
| chr2:232647416 | G | C | 122 | a0001c0001t0001g0024 a0001c0001t0001g0194 a0001c0001t0001g0315 others(119): Show |
130 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(127): Show |
intron_variant | MODIFIER | c.302+13410G>C | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232647416 | |||||||
| chr2:232647643 | C | CT | 6 | a0001c0001t0005g0286 a0001c0001t0008g0285 a0001c0001t0008g0287 others(3): Show |
6 | HG01891.hp1 HG02257.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.302+13647dupT | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 232647643 | ||||||
| chr2:232647643 | C | CTTTTTTT others(1): Show |
65 | a0001c0001t0001g0172 a0001c0001t0001g0194 a0001c0001t0001g0315 others(62): Show |
71 | HG00099.hp1 HG00544.hp1 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.302+13640_302+1364 others(12): Show |
EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 232647643 | ||||||
| chr2:232647643 | C | CTTTTTTT others(2): Show |
106 | a0001c0001t0001g0019 a0001c0001t0001g0024 a0001c0001t0001g0033 others(103): Show |
108 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.302+13639_302+1364 others(13): Show |
EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 232647643 | ||||||
| chr2:232647643 | C | CTTTTTTT others(3): Show |
14 | a0001c0001t0001g0012 a0001c0001t0001g0036 a0001c0001t0001g0265 others(11): Show |
14 | HG01099.hp1 HG01106.hp2 HG01433.hp2 others(11): Show |
intron_variant | MODIFIER | c.302+13638_302+1364 others(14): Show |
EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 232647643 | ||||||
| chr2:232647879 | C | T | 20 | a0001c0001t0001g0033 a0001c0001t0001g0172 a0001c0001t0003g0032 others(17): Show |
20 | HG00323.hp1 HG01243.hp1 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.302+13873C>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232647879 | |||||||
| chr2:232647982 | G | A | 1 | a0002c0003t0001g0166 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.302+13976G>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232647982 | |||||||
| chr2:232648005 | C | T | 5 | a0001c0001t0005g0010 a0001c0001t0005g0281 a0001c0001t0005g0282 others(2): Show |
6 | HG02886.hp1 HG03453.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.302+13999C>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232648005 | |||||||
| chr2:232648132 | G | A | 5 | a0001c0001t0006g0035 a0001c0001t0006g0097 a0001c0001t0006g0098 others(2): Show |
5 | HG01109.hp2 HG02258.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.302+14126G>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232648132 | |||||||
| chr2:232648224 | G | A | 1 | a0001c0001t0001g0265 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.302+14218G>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232648224 | |||||||
| chr2:232648386 | TGGGAGTG others(1847): Show |
T | 1 | a0001c0001t0013g0039 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.302+14384_303-1255 others(4): Show |
EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 232648386 | ||||||
| chr2:232648465 | C | A | 194 | a0001c0001t0001g0012 a0001c0001t0001g0019 a0001c0001t0001g0024 others(191): Show |
203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.303-14337C>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232648465 | |||||||
| chr2:232648643 | G | C | 2 | a0001c0004t0004g0064 a0001c0004t0004g0065 |
2 | NA18972.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.303-14159G>C | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232648643 | |||||||
| chr2:232648672 | C | T | 3 | a0001c0001t0001g0024 a0001c0001t0006g0025 a0001c0001t0006g0026 |
3 | HG02280.hp1 HG02886.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.303-14130C>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232648672 | |||||||
| chr2:232648687 | G | T | 5 | a0001c0001t0001g0308 a0001c0001t0001g0356 a0001c0001t0003g0357 others(2): Show |
5 | HG02145.hp1 HG02257.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.303-14115G>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232648687 | |||||||
| chr2:232648727 | A | G | 2 | a0001c0001t0001g0019 a0001c0001t0001g0265 |
2 | HG03540.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.303-14075A>G | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232648727 | |||||||
| chr2:232648788 | G | A | 1 | a0001c0004t0006g0191 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.303-14014G>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232648788 | |||||||
| chr2:232648849 | C | G | 5 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(2): Show |
5 | HG00544.hp2 HG02300.hp1 NA18951.hp2 others(2): Show |
intron_variant | MODIFIER | c.303-13953C>G | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232648849 | |||||||
| chr2:232648947 | G | A | 1 | a0002c0002t0001g0205 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.303-13855G>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232648947 | |||||||
| chr2:232649030 | T | C | 1 | a0001c0001t0006g0097 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.303-13772T>C | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232649030 | |||||||
| chr2:232649032 | G | T | 1 | a0001c0001t0003g0247 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.303-13770G>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232649032 | |||||||
| chr2:232649144 | A | G | 1 | a0002c0002t0001g0255 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.303-13658A>G | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232649144 | |||||||
| chr2:232649165 | C | T | 6 | a0001c0001t0006g0035 a0001c0001t0006g0097 a0001c0001t0006g0098 others(3): Show |
6 | HG01109.hp2 HG02258.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.303-13637C>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232649165 | |||||||
| chr2:232649237 | T | C | 1 | a0003c0005t0002g0015 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.303-13565T>C | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232649237 | |||||||
| chr2:232649243 | C | T | 6 | a0001c0001t0005g0286 a0001c0001t0008g0285 a0001c0001t0008g0287 others(3): Show |
6 | HG01891.hp1 HG02257.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.303-13559C>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232649243 | |||||||
| chr2:232649256 | G | A | 32 | a0001c0001t0001g0033 a0001c0001t0001g0308 a0001c0001t0001g0356 others(29): Show |
32 | HG00280.hp1 HG00642.hp1 HG01175.hp2 others(29): Show |
intron_variant | MODIFIER | c.303-13546G>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232649256 | |||||||
| chr2:232649308 | C | T | 5 | a0001c0001t0006g0035 a0001c0001t0006g0097 a0001c0001t0006g0098 others(2): Show |
5 | HG01109.hp2 HG02258.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.303-13494C>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232649308 | |||||||
| chr2:232649531 | A | G | 1 | a0001c0001t0011g0038 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.303-13271A>G | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232649531 | |||||||
| chr2:232649599 | A | G | 20 | a0001c0001t0001g0012 a0001c0001t0001g0036 a0001c0001t0001g0048 others(17): Show |
20 | HG00544.hp2 HG01099.hp1 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.303-13203A>G | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232649599 | |||||||
| chr2:232649926 | G | T | 210 | a0001c0001t0001g0012 a0001c0001t0001g0019 a0001c0001t0001g0024 others(207): Show |
221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.303-12876G>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232649926 | |||||||
| chr2:232649928 | G | C | 204 | a0001c0001t0001g0012 a0001c0001t0001g0019 a0001c0001t0001g0024 others(201): Show |
215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.303-12874G>C | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232649928 | |||||||
| chr2:232650042 | G | A | 1 | a0003c0005t0002g0015 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.303-12760G>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232650042 | |||||||
| chr2:232650104 | G | A | 5 | a0001c0001t0001g0308 a0001c0001t0001g0356 a0001c0001t0003g0357 others(2): Show |
5 | HG02145.hp1 HG02257.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.303-12698G>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232650104 | |||||||
| chr2:232650291 | C | CT | 24 | a0001c0001t0001g0052 a0001c0001t0001g0308 a0001c0001t0003g0270 others(21): Show |
24 | HG01891.hp1 HG02135.hp2 HG02293.hp2 others(21): Show |
intron_variant | MODIFIER | c.303-12491dupT | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 232650291 | ||||||
| chr2:232650291 | CT | C | 28 | a0001c0001t0001g0036 a0001c0001t0001g0048 a0001c0001t0001g0049 others(25): Show |
28 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(25): Show |
intron_variant | MODIFIER | c.303-12491delT | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 232650291 | ||||||
| chr2:232650397 | C | T | 2 | a0003c0005t0001g0028 a0008c0013t0001g0027 |
2 | HG02683.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.303-12405C>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232650397 | |||||||
| chr2:232650537 | A | G | 202 | a0001c0001t0001g0012 a0001c0001t0001g0019 a0001c0001t0001g0024 others(199): Show |
213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): Show |
intron_variant | MODIFIER | c.303-12265A>G | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232650537 | |||||||
| chr2:232650559 | G | GCTGAGAT others(29): Show |
33 | a0001c0001t0001g0019 a0001c0001t0001g0033 a0001c0001t0001g0265 others(30): Show |
33 | HG01109.hp1 HG01361.hp1 HG01891.hp1 others(30): Show |
intron_variant | MODIFIER | c.303-12241_303-1224 others(40): Show |
EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 232650559 | ||||||
| chr2:232650560 | C | CT | 29 | a0001c0001t0002g0155 a0001c0001t0002g0181 a0001c0001t0002g0341 others(26): Show |
30 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(27): Show |
intron_variant | MODIFIER | c.303-12216dupT | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 232650560 | ||||||
| chr2:232650560 | C | CTGAGATT others(30): Show |
13 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(10): Show |
13 | HG00544.hp2 HG01109.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.303-12241_303-1224 others(41): Show |
EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 232650560 | ||||||
| chr2:232650560 | C | CTGAGATT others(31): Show |
1 | a0001c0001t0021g0272 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.303-12241_303-1224 others(42): Show |
EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 232650560 | ||||||
| chr2:232650560 | CT | C | 7 | a0001c0001t0002g0325 a0001c0001t0002g0326 a0001c0004t0001g0157 others(4): Show |
7 | HG02965.hp2 HG03834.hp2 NA18948.hp1 others(4): Show |
intron_variant | MODIFIER | c.303-12216delT | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 232650560 | ||||||
| chr2:232650561 | T | TGAGATTG others(26): Show |
3 | a0001c0001t0001g0172 a0001c0004t0004g0169 a0003c0005t0002g0015 |
3 | HG03041.hp1 HG03139.hp1 NA18942.hp2 |
intron_variant | MODIFIER | c.303-12241_303-1224 others(37): Show |
EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232650561 | |||||||
| chr2:232650561 | T | TGAGATTG others(27): Show |
25 | a0001c0001t0004g0319 a0001c0001t0004g0352 a0001c0001t0004g0353 others(22): Show |
25 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(22): Show |
intron_variant | MODIFIER | c.303-12241_303-1224 others(38): Show |
EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232650561 | |||||||
| chr2:232650561 | T | TGAGATTG others(28): Show |
135 | a0001c0001t0001g0012 a0001c0001t0001g0024 a0001c0001t0001g0036 others(132): Show |
146 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(143): Show |
intron_variant | MODIFIER | c.303-12241_303-1224 others(39): Show |
EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232650561 | |||||||
| chr2:232650562 | T | A | 1 | a0001c0001t0013g0039 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.303-12240T>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232650562 | |||||||
| chr2:232650562 | T | C | 28 | a0001c0001t0001g0172 a0001c0001t0004g0319 a0001c0001t0004g0352 others(25): Show |
28 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.303-12240T>C | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232650562 | |||||||
| chr2:232650563 | T | C | 3 | a0001c0001t0001g0172 a0001c0004t0004g0169 a0003c0005t0002g0015 |
3 | HG03041.hp1 HG03139.hp1 NA18942.hp2 |
intron_variant | MODIFIER | c.303-12239T>C | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232650563 | |||||||
| chr2:232650564 | T | TGCAGGCG others(22): Show |
1 | a0001c0001t0013g0039 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.303-12238_303-1223 others(33): Show |
EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232650564 | |||||||
| chr2:232650582 | T | C | 8 | a0001c0001t0001g0315 a0001c0001t0004g0359 a0002c0002t0001g0314 others(5): Show |
8 | HG00544.hp1 HG02027.hp2 HG02083.hp2 others(5): Show |
intron_variant | MODIFIER | c.303-12220T>C | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232650582 | |||||||
| chr2:232650603 | C | T | 1 | a0002c0002t0001g0213 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.303-12199C>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232650603 | |||||||
| chr2:232650631 | C | T | 1 | a0001c0001t0003g0266 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.303-12171C>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232650631 | |||||||
| chr2:232650870 | A | G | 2 | a0001c0001t0001g0172 a0003c0005t0002g0015 |
2 | HG03041.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.303-11932A>G | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232650870 | |||||||
| chr2:232650915 | C | T | 1 | a0001c0001t0013g0039 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.303-11887C>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232650915 | |||||||
| chr2:232651037 | C | G | 25 | a0001c0001t0004g0319 a0001c0001t0004g0352 a0001c0001t0004g0353 others(22): Show |
25 | HG00280.hp1 HG00323.hp1 HG00642.hp1 others(22): Show |
intron_variant | MODIFIER | c.303-11765C>G | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232651037 | |||||||
| chr2:232651058 | A | AGG | 6 | a0001c0001t0003g0228 a0001c0001t0003g0266 a0001c0001t0003g0268 others(3): Show |
6 | HG02572.hp1 HG02976.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.303-11742_303-1174 others(6): Show |
EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 232651058 | ||||||
| chr2:232651105 | C | G | 5 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(2): Show |
5 | HG00544.hp2 HG02300.hp1 NA18951.hp2 others(2): Show |
intron_variant | MODIFIER | c.303-11697C>G | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232651105 | |||||||
| chr2:232651244 | G | T | 14 | a0001c0001t0001g0012 a0001c0001t0001g0036 a0001c0001t0003g0037 others(11): Show |
14 | HG01099.hp1 HG01106.hp2 HG01433.hp2 others(11): Show |
intron_variant | MODIFIER | c.303-11558G>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232651244 | |||||||
| chr2:232651259 | C | T | 1 | a0001c0001t0004g0320 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.303-11543C>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232651259 | |||||||
| chr2:232651587 | C | G | 121 | a0001c0001t0001g0024 a0001c0001t0001g0194 a0001c0001t0001g0315 others(118): Show |
129 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(126): Show |
intron_variant | MODIFIER | c.303-11215C>G | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232651587 | |||||||
| chr2:232651798 | G | A | 2 | a0001c0001t0001g0019 a0001c0001t0001g0265 |
2 | HG03540.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.303-11004G>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232651798 | |||||||
| chr2:232651824 | A | AAAAC | 169 | a0001c0001t0001g0012 a0001c0001t0001g0024 a0001c0001t0001g0036 others(166): Show |
177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
intron_variant | MODIFIER | c.303-10970_303-1096 others(8): Show |
EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 232651824 | ||||||
| chr2:232651944 | C | CCT | 212 | a0001c0001t0001g0012 a0001c0001t0001g0019 a0001c0001t0001g0024 others(209): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.303-10857_303-1085 others(6): Show |
EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 232651944 | ||||||
| chr2:232652319 | T | C | 3 | a0001c0001t0006g0269 a0001c0004t0006g0191 a0002c0002t0001g0280 |
3 | HG02818.hp1 HG02818.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.303-10483T>C | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232652319 | |||||||
| chr2:232652470 | C | A | 9 | a0001c0004t0002g0113 a0001c0004t0002g0114 a0001c0004t0002g0134 others(6): Show |
9 | HG00558.hp1 HG02040.hp1 HG02040.hp2 others(6): Show |
intron_variant | MODIFIER | c.303-10332C>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232652470 | |||||||
| chr2:232652525 | A | T | 1 | a0002c0003t0001g0166 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.303-10277A>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232652525 | |||||||
| chr2:232652635 | A | C | 1 | a0001c0001t0005g0264 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.303-10167A>C | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232652635 | |||||||
| chr2:232652693 | C | T | 1 | a0003c0005t0011g0023 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.303-10109C>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232652693 | |||||||
| chr2:232652991 | G | T | 187 | a0001c0001t0001g0012 a0001c0001t0001g0019 a0001c0001t0001g0024 others(184): Show |
198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
intron_variant | MODIFIER | c.303-9811G>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232652991 | |||||||
| chr2:232653017 | C | T | 1 | a0002c0003t0001g0091 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.303-9785C>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232653017 | |||||||
| chr2:232653062 | C | T | 104 | a0001c0001t0001g0024 a0001c0001t0001g0194 a0001c0001t0002g0200 others(101): Show |
112 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(109): Show |
intron_variant | MODIFIER | c.303-9740C>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232653062 | |||||||
| chr2:232653076 | C | T | 14 | a0001c0001t0005g0300 a0001c0001t0005g0303 a0001c0001t0006g0277 others(11): Show |
14 | HG00280.hp1 HG00642.hp1 HG01175.hp2 others(11): Show |
intron_variant | MODIFIER | c.303-9726C>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232653076 | |||||||
| chr2:232653089 | G | A | 1 | a0002c0002t0001g0195 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.303-9713G>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232653089 | |||||||
| chr2:232653151 | G | A | 2 | a0002c0002t0001g0318 a0002c0002t0001g0327 |
2 | NA19056.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.303-9651G>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232653151 | |||||||
| chr2:232653159 | A | C | 1 | a0001c0001t0001g0172 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.303-9643A>C | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232653159 | |||||||
| chr2:232653208 | G | A | 3 | a0001c0001t0001g0024 a0001c0001t0006g0025 a0001c0001t0006g0026 |
3 | HG02280.hp1 HG02886.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.303-9594G>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232653208 | |||||||
| chr2:232653299 | T | A | 2 | a0001c0001t0002g0367 a0001c0001t0002g0368 |
2 | HG01496.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.303-9503T>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232653299 | |||||||
| chr2:232653319 | C | G | 1 | a0001c0004t0003g0061 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.303-9483C>G | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232653319 | |||||||
| chr2:232653330 | G | A | 6 | a0001c0001t0003g0239 a0001c0001t0006g0035 a0001c0001t0006g0097 others(3): Show |
6 | HG01109.hp2 HG02258.hp2 HG02602.hp2 others(3): Show |
intron_variant | MODIFIER | c.303-9472G>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232653330 | |||||||
| chr2:232653488 | A | G | 14 | a0001c0001t0005g0300 a0001c0001t0005g0303 a0001c0001t0006g0277 others(11): Show |
14 | HG00280.hp1 HG00642.hp1 HG01175.hp2 others(11): Show |
intron_variant | MODIFIER | c.303-9314A>G | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232653488 | |||||||
| chr2:232653493 | G | A | 5 | a0001c0001t0006g0035 a0001c0001t0006g0097 a0001c0001t0006g0098 others(2): Show |
5 | HG01109.hp2 HG02258.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.303-9309G>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232653493 | |||||||
| chr2:232653541 | C | T | 1 | a0003c0005t0002g0015 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.303-9261C>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232653541 | |||||||
| chr2:232653585 | C | T | 1 | a0001c0001t0023g0309 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.303-9217C>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232653585 | |||||||
| chr2:232653676 | T | C | 7 | a0001c0004t0003g0083 a0001c0004t0003g0183 a0001c0004t0003g0185 others(4): Show |
7 | NA18939.hp2 NA18944.hp1 NA18945.hp2 others(4): Show |
intron_variant | MODIFIER | c.303-9126T>C | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232653676 | |||||||
| chr2:232653705 | G | A | 2 | a0001c0001t0007g0002 a0001c0001t0007g0295 |
4 | HG02280.hp2 HG02809.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.303-9097G>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232653705 | |||||||
| chr2:232653934 | C | T | 1 | a0002c0002t0022g0263 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.303-8868C>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232653934 | |||||||
| chr2:232653972 | C | A | 1 | a0002c0003t0001g0091 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.303-8830C>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232653972 | |||||||
| chr2:232653982 | A | C | 11 | a0001c0004t0003g0082 a0001c0004t0003g0083 a0001c0004t0003g0183 others(8): Show |
11 | HG02135.hp2 NA18939.hp2 NA18944.hp1 others(8): Show |
intron_variant | MODIFIER | c.303-8820A>C | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232653982 | |||||||
| chr2:232654004 | C | T | 1 | a0002c0002t0001g0279 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.303-8798C>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232654004 | |||||||
| chr2:232654024 | T | G | 132 | a0001c0001t0001g0024 a0001c0001t0001g0172 a0001c0001t0001g0194 others(129): Show |
140 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(137): Show |
intron_variant | MODIFIER | c.303-8778T>G | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232654024 | |||||||
| chr2:232654206 | C | CA | 10 | a0001c0001t0001g0077 a0001c0001t0003g0032 a0001c0001t0003g0037 others(7): Show |
10 | HG00140.hp2 HG00280.hp2 HG01346.hp1 others(7): Show |
intron_variant | MODIFIER | c.303-8580dupA | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 232654206 | ||||||
| chr2:232654224 | A | G | 2 | a0001c0001t0001g0265 a0001c0001t0013g0039 |
2 | HG03195.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.303-8578A>G | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232654224 | |||||||
| chr2:232654305 | C | T | 1 | a0001c0001t0005g0300 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.303-8497C>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232654305 | |||||||
| chr2:232654375 | G | A | 23 | a0001c0001t0001g0019 a0001c0001t0001g0048 a0001c0001t0001g0049 others(20): Show |
23 | HG00323.hp1 HG00544.hp2 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.303-8427G>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232654375 | |||||||
| chr2:232654416 | C | CT | 54 | a0001c0001t0001g0012 a0001c0001t0001g0024 a0001c0001t0001g0036 others(51): Show |
56 | HG00642.hp2 HG01099.hp1 HG01106.hp2 others(53): Show |
intron_variant | MODIFIER | c.303-8364dupT | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 232654416 | ||||||
| chr2:232654416 | C | CTT | 53 | a0001c0001t0001g0019 a0001c0001t0001g0048 a0001c0001t0001g0049 others(50): Show |
55 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(52): Show |
intron_variant | MODIFIER | c.303-8365_303-8364d others(4): Show |
EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 232654416 | ||||||
| chr2:232654416 | C | CTTT | 17 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0265 others(14): Show |
17 | HG00642.hp1 HG01109.hp2 HG01175.hp2 others(14): Show |
intron_variant | MODIFIER | c.303-8366_303-8364d others(5): Show |
EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 232654416 | ||||||
| chr2:232654416 | CTTTTTTT others(5): Show |
C | 5 | a0001c0001t0001g0033 a0001c0001t0004g0031 a0001c0001t0006g0030 others(2): Show |
5 | HG01243.hp1 HG02055.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.303-8375_303-8364d others(14): Show |
EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 232654416 | ||||||
| chr2:232654420 | T | C | 2 | a0001c0001t0007g0291 a0002c0002t0005g0292 |
2 | HG01884.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.303-8382T>C | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232654420 | |||||||
| chr2:232654457 | G | T | 36 | a0001c0001t0001g0019 a0001c0001t0001g0048 a0001c0001t0001g0049 others(33): Show |
36 | HG00280.hp1 HG00544.hp2 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.303-8345G>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232654457 | |||||||
| chr2:232654534 | C | T | 1 | a0002c0002t0022g0263 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.303-8268C>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232654534 | |||||||
| chr2:232654575 | C | T | 1 | a0002c0002t0022g0263 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.303-8227C>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232654575 | |||||||
| chr2:232654638 | G | C | 1 | a0001c0004t0004g0169 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.303-8164G>C | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232654638 | |||||||
| chr2:232654696 | G | C | 23 | a0001c0001t0001g0019 a0001c0001t0001g0048 a0001c0001t0001g0049 others(20): Show |
23 | HG00544.hp2 HG01109.hp2 HG02083.hp2 others(20): Show |
intron_variant | MODIFIER | c.303-8106G>C | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232654696 | |||||||
| chr2:232654850 | G | A | 6 | a0001c0001t0006g0277 a0001c0001t0006g0278 a0001c0004t0006g0041 others(3): Show |
6 | HG02809.hp2 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.303-7952G>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232654850 | |||||||
| chr2:232654892 | C | A | 1 | a0001c0006t0005g0366 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.303-7910C>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232654892 | |||||||
| chr2:232654915 | C | T | 1 | a0002c0002t0001g0340 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.303-7887C>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232654915 | |||||||
| chr2:232655053 | C | T | 1 | a0001c0001t0002g0179 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.303-7749C>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232655053 | |||||||
| chr2:232655259 | GTCC | G | 4 | a0001c0001t0001g0308 a0001c0001t0001g0356 a0001c0001t0007g0290 others(1): Show |
4 | HG02257.hp1 HG02572.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.303-7538_303-7536d others(5): Show |
EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 232655259 | ||||||
| chr2:232655263 | T | A | 4 | a0001c0001t0003g0307 a0001c0001t0016g0216 a0001c0004t0002g0262 others(1): Show |
4 | HG02109.hp1 HG02976.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.303-7539T>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232655263 | |||||||
| chr2:232655510 | G | A | 8 | a0001c0001t0001g0172 a0001c0001t0005g0364 a0001c0006t0001g0034 others(5): Show |
8 | HG01891.hp2 HG02965.hp1 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.303-7292G>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232655510 | |||||||
| chr2:232655544 | A | T | 185 | a0001c0001t0001g0012 a0001c0001t0001g0019 a0001c0001t0001g0024 others(182): Show |
193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.303-7258A>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232655544 | |||||||
| chr2:232655664 | T | G | 1 | a0001c0004t0002g0113 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.303-7138T>G | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232655664 | |||||||
| chr2:232655669 | A | G | 138 | a0001c0001t0001g0024 a0001c0001t0001g0172 a0001c0001t0001g0194 others(135): Show |
146 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(143): Show |
intron_variant | MODIFIER | c.303-7133A>G | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232655669 | |||||||
| chr2:232655745 | A | G | 5 | a0001c0001t0006g0035 a0001c0001t0006g0097 a0001c0001t0006g0098 others(2): Show |
5 | HG01109.hp2 HG02258.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.303-7057A>G | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232655745 | |||||||
| chr2:232655802 | C | CT | 12 | a0001c0001t0002g0322 a0001c0001t0002g0339 a0001c0001t0003g0228 others(9): Show |
12 | HG01975.hp2 HG02572.hp1 HG02976.hp1 others(9): Show |
intron_variant | MODIFIER | c.303-6978dupT | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 232655802 | ||||||
| chr2:232655802 | C | CTT | 9 | a0001c0001t0003g0032 a0001c0001t0003g0037 a0001c0001t0006g0035 others(6): Show |
9 | HG00735.hp2 HG01109.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.303-6979_303-6978d others(4): Show |
EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 232655802 | ||||||
| chr2:232655802 | CT | C | 21 | a0001c0001t0001g0033 a0001c0001t0001g0308 a0001c0001t0001g0356 others(18): Show |
22 | HG01243.hp1 HG02055.hp1 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.303-6978delT | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 232655802 | ||||||
| chr2:232655802 | CTTTTTTT others(4): Show |
C | 133 | a0001c0001t0001g0024 a0001c0001t0001g0172 a0001c0001t0001g0194 others(130): Show |
141 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(138): Show |
intron_variant | MODIFIER | c.303-6988_303-6978d others(13): Show |
EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 232655802 | ||||||
| chr2:232655808 | T | TC | 5 | a0001c0001t0005g0286 a0001c0001t0008g0285 a0001c0001t0008g0287 others(2): Show |
5 | HG01891.hp1 HG02257.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.303-6994_303-6993i others(3): Show |
EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232655808 | |||||||
| chr2:232655869 | C | T | 68 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(65): Show |
74 | HG00099.hp1 HG00323.hp2 HG00544.hp1 others(71): Show |
intron_variant | MODIFIER | c.303-6933C>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232655869 | |||||||
| chr2:232655986 | T | C | 14 | a0001c0001t0005g0300 a0001c0001t0005g0303 a0001c0001t0006g0277 others(11): Show |
14 | HG00280.hp1 HG00642.hp1 HG01175.hp2 others(11): Show |
intron_variant | MODIFIER | c.303-6816T>C | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232655986 | |||||||
| chr2:232656057 | C | T | 4 | a0001c0001t0001g0308 a0001c0001t0001g0356 a0001c0001t0007g0290 others(1): Show |
4 | HG02257.hp1 HG02572.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.303-6745C>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232656057 | |||||||
| chr2:232656058 | G | C | 1 | a0001c0004t0004g0230 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.303-6744G>C | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232656058 | |||||||
| chr2:232656184 | C | T | 2 | a0001c0001t0006g0097 a0001c0001t0021g0272 |
2 | HG02630.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.303-6618C>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232656184 | |||||||
| chr2:232656225 | G | A | 1 | a0001c0001t0005g0264 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.303-6577G>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232656225 | |||||||
| chr2:232656226 | T | C | 1 | a0001c0001t0002g0142 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.303-6576T>C | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232656226 | |||||||
| chr2:232656232 | T | C | 138 | a0001c0001t0001g0024 a0001c0001t0001g0172 a0001c0001t0001g0194 others(135): Show |
146 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(143): Show |
intron_variant | MODIFIER | c.303-6570T>C | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232656232 | |||||||
| chr2:232656426 | CT | C | 7 | a0001c0001t0002g0258 a0001c0001t0003g0234 a0001c0004t0002g0131 others(4): Show |
7 | HG00140.hp1 HG01070.hp2 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.303-6359delT | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 232656426 | ||||||
| chr2:232656513 | C | T | 1 | a0002c0002t0001g0198 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.303-6289C>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232656513 | |||||||
| chr2:232656530 | G | T | 2 | a0001c0001t0006g0277 a0001c0001t0006g0278 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.303-6272G>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232656530 | |||||||
| chr2:232656609 | T | A | 1 | a0002c0002t0022g0263 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.303-6193T>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232656609 | |||||||
| chr2:232656904 | G | A | 1 | a0001c0001t0003g0235 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.303-5898G>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232656904 | |||||||
| chr2:232656917 | C | T | 9 | a0001c0001t0005g0300 a0001c0001t0005g0303 a0001c0001t0007g0304 others(6): Show |
9 | HG00280.hp1 HG00642.hp1 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.303-5885C>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232656917 | |||||||
| chr2:232656926 | G | A | 11 | a0001c0004t0003g0082 a0001c0004t0003g0083 a0001c0004t0003g0183 others(8): Show |
11 | HG02135.hp2 NA18939.hp2 NA18944.hp1 others(8): Show |
intron_variant | MODIFIER | c.303-5876G>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232656926 | |||||||
| chr2:232657006 | C | T | 1 | a0001c0001t0001g0019 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.303-5796C>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232657006 | |||||||
| chr2:232657022 | C | G | 7 | a0001c0001t0003g0032 a0001c0001t0003g0037 a0001c0001t0003g0228 others(4): Show |
7 | HG02145.hp2 HG02572.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.303-5780C>G | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232657022 | |||||||
| chr2:232657028 | C | G | 1 | a0001c0001t0001g0051 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.303-5774C>G | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232657028 | |||||||
| chr2:232657030 | T | C | 1 | a0001c0001t0001g0051 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.303-5772T>C | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232657030 | |||||||
| chr2:232657031 | G | T | 1 | a0001c0001t0001g0051 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.303-5771G>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232657031 | |||||||
| chr2:232657254 | A | C | 6 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(3): Show |
6 | HG00544.hp2 HG02083.hp2 HG02300.hp1 others(3): Show |
intron_variant | MODIFIER | c.303-5548A>C | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232657254 | |||||||
| chr2:232657320 | T | C | 14 | a0001c0001t0005g0300 a0001c0001t0005g0303 a0001c0001t0006g0277 others(11): Show |
14 | HG00280.hp1 HG00642.hp1 HG01175.hp2 others(11): Show |
intron_variant | MODIFIER | c.303-5482T>C | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232657320 | |||||||
| chr2:232657322 | C | A | 3 | a0001c0001t0020g0276 a0001c0004t0004g0164 a0001c0004t0004g0165 |
3 | HG03041.hp2 HG03098.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.303-5480C>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232657322 | |||||||
| chr2:232657332 | G | A | 12 | a0001c0001t0001g0172 a0001c0001t0003g0307 a0001c0001t0005g0364 others(9): Show |
12 | HG01891.hp2 HG02109.hp1 HG02965.hp1 others(9): Show |
intron_variant | MODIFIER | c.303-5470G>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232657332 | |||||||
| chr2:232657436 | A | G | 1 | a0001c0004t0003g0094 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.303-5366A>G | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232657436 | |||||||
| chr2:232657467 | G | C | 42 | a0001c0001t0001g0172 a0001c0001t0002g0246 a0001c0001t0002g0252 others(39): Show |
44 | HG00099.hp2 HG00140.hp1 HG00609.hp2 others(41): Show |
intron_variant | MODIFIER | c.303-5335G>C | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232657467 | |||||||
| chr2:232657548 | G | A | 1 | a0001c0001t0001g0019 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.303-5254G>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232657548 | |||||||
| chr2:232657668 | G | A | 6 | a0001c0001t0005g0364 a0001c0006t0001g0034 a0001c0006t0001g0267 others(3): Show |
6 | HG01891.hp2 HG02965.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.303-5134G>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232657668 | |||||||
| chr2:232657812 | C | CA | 23 | a0001c0001t0001g0033 a0001c0001t0001g0051 a0001c0001t0003g0270 others(20): Show |
26 | HG01243.hp1 HG02055.hp1 HG02145.hp1 others(23): Show |
intron_variant | MODIFIER | c.303-4977dupA | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 232657812 | ||||||
| chr2:232657869 | T | C | 2 | a0001c0001t0002g0203 a0003c0005t0002g0060 |
2 | HG03654.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.303-4933T>C | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232657869 | |||||||
| chr2:232657894 | C | CT | 3 | a0001c0001t0001g0012 a0001c0001t0005g0297 a0005c0008t0001g0022 |
3 | HG01106.hp2 HG01433.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.303-4904dupT | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 232657894 | ||||||
| chr2:232657899 | C | CT | 68 | a0001c0001t0001g0019 a0001c0001t0001g0051 a0001c0001t0001g0172 others(65): Show |
70 | HG00099.hp2 HG00140.hp1 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.303-4884dupT | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 232657899 | ||||||
| chr2:232657899 | C | CTT | 7 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(4): Show |
7 | HG00544.hp2 HG01109.hp1 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.303-4885_303-4884d others(4): Show |
EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 232657899 | ||||||
| chr2:232657899 | C | T | 10 | a0001c0001t0001g0012 a0001c0001t0001g0036 a0001c0001t0005g0297 others(7): Show |
10 | HG01099.hp1 HG01106.hp2 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.303-4903C>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232657899 | |||||||
| chr2:232657904 | T | C | 2 | a0001c0001t0001g0265 a0001c0001t0005g0264 |
2 | HG03540.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.303-4898T>C | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232657904 | |||||||
| chr2:232657969 | C | T | 24 | a0001c0001t0001g0033 a0001c0001t0001g0308 a0001c0001t0001g0356 others(21): Show |
27 | HG01243.hp1 HG02055.hp1 HG02145.hp1 others(24): Show |
intron_variant | MODIFIER | c.303-4833C>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232657969 | |||||||
| chr2:232658011 | C | T | 1 | a0001c0001t0001g0019 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.303-4791C>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232658011 | |||||||
| chr2:232658138 | G | C | 1 | a0002c0002t0022g0263 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.303-4664G>C | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232658138 | |||||||
| chr2:232658317 | A | G | 1 | a0001c0001t0013g0039 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.303-4485A>G | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232658317 | |||||||
| chr2:232658355 | G | A | 13 | a0001c0001t0003g0270 a0001c0001t0003g0275 a0001c0001t0003g0357 others(10): Show |
16 | HG02145.hp1 HG02280.hp2 HG02615.hp2 others(13): Show |
intron_variant | MODIFIER | c.303-4447G>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232658355 | |||||||
| chr2:232658365 | A | G | 56 | a0001c0001t0001g0172 a0001c0001t0002g0246 a0001c0001t0002g0252 others(53): Show |
58 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.303-4437A>G | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232658365 | |||||||
| chr2:232658389 | AGCCT | A | 112 | a0001c0001t0001g0012 a0001c0001t0001g0019 a0001c0001t0001g0033 others(109): Show |
117 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.303-4406_303-4403d others(6): Show |
EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 232658389 | ||||||
| chr2:232658439 | G | A | 1 | a0001c0001t0001g0265 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.303-4363G>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232658439 | |||||||
| chr2:232658473 | C | T | 5 | a0001c0001t0006g0035 a0001c0001t0006g0097 a0001c0001t0006g0098 others(2): Show |
5 | HG01109.hp2 HG02258.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.303-4329C>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232658473 | |||||||
| chr2:232658474 | G | A | 1 | a0002c0002t0001g0143 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.303-4328G>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232658474 | |||||||
| chr2:232658526 | C | T | 1 | a0002c0002t0022g0263 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.303-4276C>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232658526 | |||||||
| chr2:232658527 | G | A | 1 | a0002c0002t0001g0279 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.303-4275G>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232658527 | |||||||
| chr2:232658528 | A | G | 1 | a0001c0004t0004g0081 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.303-4274A>G | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232658528 | |||||||
| chr2:232658566 | C | G | 1 | a0002c0002t0001g0279 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.303-4236C>G | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232658566 | |||||||
| chr2:232658599 | G | A | 11 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(8): Show |
11 | HG00544.hp2 HG01109.hp2 HG02083.hp2 others(8): Show |
intron_variant | MODIFIER | c.303-4203G>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232658599 | |||||||
| chr2:232658774 | T | C | 11 | a0001c0001t0001g0012 a0001c0001t0001g0036 a0001c0001t0001g0265 others(8): Show |
11 | HG01099.hp1 HG01106.hp2 HG01433.hp2 others(8): Show |
intron_variant | MODIFIER | c.303-4028T>C | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232658774 | |||||||
| chr2:232658787 | T | A | 1 | a0002c0003t0001g0166 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.303-4015T>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232658787 | |||||||
| chr2:232658907 | G | A | 62 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(59): Show |
64 | HG00099.hp2 HG00140.hp1 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.303-3895G>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232658907 | |||||||
| chr2:232659142 | C | T | 1 | a0002c0003t0001g0073 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.303-3660C>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232659142 | |||||||
| chr2:232659711 | C | T | 1 | a0001c0001t0001g0077 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.303-3091C>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232659711 | |||||||
| chr2:232659738 | GACTA | G | 19 | a0001c0001t0001g0077 a0001c0001t0002g0013 a0001c0001t0002g0117 others(16): Show |
19 | HG00140.hp2 HG00280.hp2 HG01106.hp1 others(16): Show |
intron_variant | MODIFIER | c.303-3058_303-3055d others(6): Show |
EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 232659738 | ||||||
| chr2:232659815 | T | A | 1 | a0003c0005t0002g0015 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.303-2987T>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232659815 | |||||||
| chr2:232659834 | G | T | 1 | a0002c0003t0001g0212 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.303-2968G>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232659834 | |||||||
| chr2:232659874 | G | C | 1 | a0001c0001t0005g0264 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.303-2928G>C | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232659874 | |||||||
| chr2:232660050 | A | G | 2 | a0001c0004t0003g0083 a0001c0004t0003g0187 |
2 | NA18939.hp2 NA18946.hp1 |
intron_variant | MODIFIER | c.303-2752A>G | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232660050 | |||||||
| chr2:232660070 | G | C | 1 | a0002c0003t0001g0110 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.303-2732G>C | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232660070 | |||||||
| chr2:232660130 | A | G | 2 | a0002c0003t0001g0112 a0002c0003t0014g0116 |
2 | HG03831.hp2 NA18941.hp2 |
intron_variant | MODIFIER | c.303-2672A>G | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232660130 | |||||||
| chr2:232660171 | ATTTAT | A | 6 | a0001c0001t0006g0035 a0001c0001t0006g0097 a0001c0001t0006g0098 others(3): Show |
6 | HG01109.hp2 HG02258.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.303-2613_303-2609d others(7): Show |
EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 232660171 | ||||||
| chr2:232660190 | A | AT | 43 | a0001c0001t0002g0013 a0001c0001t0002g0246 a0001c0001t0002g0252 others(40): Show |
45 | HG00099.hp2 HG00140.hp1 HG00609.hp2 others(42): Show |
intron_variant | MODIFIER | c.303-2609dupT | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 232660190 | ||||||
| chr2:232660194 | A | T | 1 | a0002c0002t0001g0257 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.303-2608A>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232660194 | |||||||
| chr2:232660201 | TA | T | 9 | a0001c0001t0001g0012 a0001c0001t0001g0019 a0001c0001t0001g0036 others(6): Show |
9 | HG01099.hp1 HG01106.hp2 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.303-2600delA | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232660201 | |||||||
| chr2:232660202 | A | T | 14 | a0001c0001t0001g0024 a0001c0001t0009g0273 a0001c0004t0001g0223 others(11): Show |
14 | HG00609.hp1 HG03486.hp1 HG06807.hp2 others(11): Show |
intron_variant | MODIFIER | c.303-2600A>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232660202 | |||||||
| chr2:232660202 | AT | A | 21 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(18): Show |
21 | HG00544.hp2 HG01109.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.303-2590delT | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 232660202 | ||||||
| chr2:232660202 | ATT | A | 193 | a0001c0001t0001g0033 a0001c0001t0001g0052 a0001c0001t0001g0265 others(190): Show |
204 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(201): Show |
intron_variant | MODIFIER | c.303-2591_303-2590d others(4): Show |
EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 232660202 | ||||||
| chr2:232660204 | T | TTA | 44 | a0001c0001t0002g0013 a0001c0001t0002g0246 a0001c0001t0002g0252 others(41): Show |
46 | HG00099.hp2 HG00140.hp1 HG00609.hp2 others(43): Show |
intron_variant | MODIFIER | c.303-2597_303-2596i others(4): Show |
EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 232660204 | ||||||
| chr2:232660235 | C | T | 124 | a0001c0001t0001g0033 a0001c0001t0001g0052 a0001c0001t0001g0265 others(121): Show |
130 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.303-2567C>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232660235 | |||||||
| chr2:232660257 | C | T | 2 | a0001c0001t0001g0356 a0001c0001t0007g0290 |
2 | HG02257.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.303-2545C>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232660257 | |||||||
| chr2:232660287 | T | C | 8 | a0001c0001t0005g0300 a0001c0001t0005g0303 a0001c0001t0007g0304 others(5): Show |
8 | HG00280.hp1 HG01175.hp2 HG02683.hp2 others(5): Show |
intron_variant | MODIFIER | c.303-2515T>C | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232660287 | |||||||
| chr2:232660388 | A | G | 2 | a0001c0001t0001g0172 a0001c0001t0011g0038 |
2 | HG03041.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.303-2414A>G | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232660388 | |||||||
| chr2:232660405 | A | G | 1 | a0008c0013t0001g0027 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.303-2397A>G | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232660405 | |||||||
| chr2:232660435 | C | T | 1 | a0002c0003t0001g0084 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.303-2367C>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232660435 | |||||||
| chr2:232660446 | C | T | 6 | a0001c0001t0005g0364 a0001c0006t0001g0034 a0001c0006t0001g0267 others(3): Show |
6 | HG01891.hp2 HG02965.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.303-2356C>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232660446 | |||||||
| chr2:232660497 | G | A | 6 | a0001c0001t0006g0035 a0001c0001t0006g0097 a0001c0001t0006g0098 others(3): Show |
6 | HG01109.hp2 HG02258.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.303-2305G>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232660497 | |||||||
| chr2:232660610 | C | T | 9 | a0002c0002t0001g0214 a0002c0003t0001g0087 a0002c0003t0001g0088 others(6): Show |
9 | HG00558.hp2 NA18944.hp2 NA18952.hp2 others(6): Show |
intron_variant | MODIFIER | c.303-2192C>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232660610 | |||||||
| chr2:232660683 | A | G | 1 | a0001c0001t0002g0219 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.303-2119A>G | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232660683 | |||||||
| chr2:232660972 | C | T | 1 | a0002c0002t0015g0313 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.303-1830C>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232660972 | |||||||
| chr2:232660973 | G | A | 1 | a0001c0004t0002g0138 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.303-1829G>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232660973 | |||||||
| chr2:232661054 | A | G | 1 | a0001c0001t0005g0264 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.303-1748A>G | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232661054 | |||||||
| chr2:232661080 | G | A | 1 | a0002c0002t0005g0284 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.303-1722G>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232661080 | |||||||
| chr2:232661084 | G | A | 11 | a0001c0004t0001g0223 a0001c0004t0003g0082 a0001c0004t0003g0083 others(8): Show |
11 | HG00609.hp1 HG02135.hp2 NA18939.hp2 others(8): Show |
intron_variant | MODIFIER | c.303-1718G>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232661084 | |||||||
| chr2:232661099 | G | T | 1 | a0001c0001t0005g0264 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.303-1703G>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232661099 | |||||||
| chr2:232661103 | G | A | 1 | a0001c0001t0001g0265 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.303-1699G>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232661103 | |||||||
| chr2:232661147 | C | CA | 15 | a0001c0001t0005g0286 a0001c0001t0006g0025 a0001c0001t0006g0026 others(12): Show |
15 | HG01109.hp2 HG01891.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.303-1645dupA | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 232661147 | ||||||
| chr2:232661152 | A | C | 2 | a0002c0003t0001g0123 a0002c0003t0001g0124 |
2 | NA18947.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.303-1650A>C | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232661152 | |||||||
| chr2:232661152 | AAAAAAC | A | 99 | a0001c0001t0001g0077 a0001c0001t0001g0308 a0001c0001t0002g0013 others(96): Show |
101 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.303-1638_303-1633d others(8): Show |
EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 232661152 | ||||||
| chr2:232661201 | G | A | 3 | a0001c0001t0001g0265 a0001c0001t0004g0031 a0001c0001t0006g0030 |
3 | HG02615.hp1 HG02922.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.303-1601G>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232661201 | |||||||
| chr2:232661387 | G | A | 72 | a0001c0001t0001g0077 a0001c0001t0001g0308 a0001c0001t0002g0117 others(69): Show |
72 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(69): Show |
intron_variant | MODIFIER | c.303-1415G>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232661387 | |||||||
| chr2:232661567 | C | T | 1 | a0002c0003t0001g0101 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.303-1235C>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232661567 | |||||||
| chr2:232661568 | C | CT | 9 | a0001c0001t0001g0265 a0001c0001t0003g0032 a0001c0001t0003g0307 others(6): Show |
9 | HG02056.hp1 HG02109.hp1 HG02976.hp2 others(6): Show |
intron_variant | MODIFIER | c.303-1216dupT | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 232661568 | ||||||
| chr2:232661568 | C | CTT | 83 | a0001c0001t0002g0013 a0001c0001t0002g0200 a0001c0001t0002g0252 others(80): Show |
91 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.303-1217_303-1216d others(4): Show |
EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 232661568 | ||||||
| chr2:232661568 | C | T | 1 | a0002c0003t0001g0101 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.303-1234C>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232661568 | |||||||
| chr2:232661568 | CT | C | 139 | a0001c0001t0001g0019 a0001c0001t0001g0052 a0001c0001t0003g0245 others(136): Show |
140 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.303-1216delT | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 232661568 | ||||||
| chr2:232661568 | CTT | C | 7 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(4): Show |
7 | HG00544.hp2 HG02083.hp2 HG02300.hp1 others(4): Show |
intron_variant | MODIFIER | c.303-1217_303-1216d others(4): Show |
EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 232661568 | ||||||
| chr2:232661569 | T | C | 2 | a0001c0001t0002g0343 a0001c0001t0004g0329 |
2 | HG00621.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.303-1233T>C | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232661569 | |||||||
| chr2:232661570 | T | C | 1 | a0001c0001t0021g0272 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.303-1232T>C | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232661570 | |||||||
| chr2:232661598 | G | C | 1 | a0001c0004t0001g0221 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.303-1204G>C | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232661598 | |||||||
| chr2:232661653 | G | A | 7 | a0001c0001t0003g0032 a0001c0001t0003g0037 a0001c0001t0003g0228 others(4): Show |
7 | HG02145.hp2 HG02572.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.303-1149G>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232661653 | |||||||
| chr2:232661686 | A | G | 81 | a0001c0001t0001g0024 a0001c0001t0001g0265 a0001c0001t0002g0013 others(78): Show |
89 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.303-1116A>G | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232661686 | |||||||
| chr2:232661748 | CAG | C | 85 | a0001c0001t0002g0013 a0001c0001t0002g0252 a0001c0001t0003g0007 others(82): Show |
93 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.303-1053_303-1052d others(4): Show |
EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232661748 | |||||||
| chr2:232661760 | A | G | 5 | a0002c0002t0001g0226 a0002c0002t0001g0227 a0003c0005t0001g0029 others(2): Show |
6 | HG00733.hp2 HG00735.hp1 HG01074.hp2 others(3): Show |
intron_variant | MODIFIER | c.303-1042A>G | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232661760 | |||||||
| chr2:232661848 | A | G | 1 | a0001c0001t0002g0179 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.303-954A>G | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232661848 | |||||||
| chr2:232662160 | G | A | 1 | a0001c0001t0001g0012 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.303-642G>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232662160 | |||||||
| chr2:232662177 | A | G | 6 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(3): Show |
6 | HG00544.hp2 HG02083.hp2 HG02300.hp1 others(3): Show |
intron_variant | MODIFIER | c.303-625A>G | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232662177 | |||||||
| chr2:232662272 | G | A | 9 | a0001c0001t0005g0364 a0001c0001t0006g0079 a0001c0001t0008g0283 others(6): Show |
9 | HG01243.hp1 HG01891.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.303-530G>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232662272 | |||||||
| chr2:232662367 | C | G | 1 | a0002c0002t0001g0047 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.303-435C>G | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232662367 | |||||||
| chr2:232662368 | CA | C | 3 | a0001c0001t0001g0024 a0001c0001t0001g0356 a0001c0001t0007g0290 |
3 | HG02257.hp1 HG03579.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.303-433delA | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232662368 | |||||||
| chr2:232662430 | C | T | 11 | a0001c0004t0001g0223 a0001c0004t0003g0082 a0001c0004t0003g0083 others(8): Show |
11 | HG00609.hp1 HG02135.hp2 NA18939.hp2 others(8): Show |
intron_variant | MODIFIER | c.303-372C>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232662430 | |||||||
| chr2:232662514 | G | A | 44 | a0001c0001t0001g0172 a0001c0001t0003g0245 a0001c0001t0003g0266 others(41): Show |
46 | HG00323.hp1 HG00408.hp2 HG00609.hp2 others(43): Show |
intron_variant | MODIFIER | c.303-288G>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232662514 | |||||||
| chr2:232662688 | G | A | 1 | a0001c0001t0004g0338 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.303-114G>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 1/3 | chr2 | 232662688 | |||||||
| chr2:232663224 | G | T | 7 | a0001c0001t0001g0024 a0001c0001t0001g0356 a0001c0001t0003g0307 others(4): Show |
7 | HG02109.hp1 HG02257.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.450+275G>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 2/3 | chr2 | 232663224 | |||||||
| chr2:232663295 | T | A | 1 | a0002c0003t0001g0070 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.450+346T>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 2/3 | chr2 | 232663295 | |||||||
| chr2:232663307 | T | C | 2 | a0001c0004t0001g0167 a0002c0003t0001g0085 |
2 | NA18950.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.450+358T>C | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 2/3 | chr2 | 232663307 | |||||||
| chr2:232663493 | C | A | 1 | a0001c0001t0001g0024 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.450+544C>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 2/3 | chr2 | 232663493 | |||||||
| chr2:232663529 | G | A | 43 | a0001c0001t0003g0266 a0001c0001t0003g0268 a0001c0001t0003g0270 others(40): Show |
45 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(42): Show |
intron_variant | MODIFIER | c.450+580G>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 2/3 | chr2 | 232663529 | |||||||
| chr2:232663570 | T | C | 1 | a0002c0003t0001g0220 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.450+621T>C | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 2/3 | chr2 | 232663570 | |||||||
| chr2:232663597 | C | G | 1 | a0002c0002t0001g0279 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.450+648C>G | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 2/3 | chr2 | 232663597 | |||||||
| chr2:232663646 | G | A | 141 | a0001c0001t0002g0200 a0001c0001t0003g0032 a0001c0001t0003g0037 others(138): Show |
148 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(145): Show |
intron_variant | MODIFIER | c.450+697G>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 2/3 | chr2 | 232663646 | |||||||
| chr2:232663746 | T | C | 44 | a0001c0001t0003g0266 a0001c0001t0003g0268 a0001c0001t0003g0270 others(41): Show |
46 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(43): Show |
intron_variant | MODIFIER | c.450+797T>C | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 2/3 | chr2 | 232663746 | |||||||
| chr2:232663749 | C | T | 7 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(4): Show |
7 | HG00544.hp2 HG02083.hp2 HG02293.hp2 others(4): Show |
intron_variant | MODIFIER | c.450+800C>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 2/3 | chr2 | 232663749 | |||||||
| chr2:232663805 | A | G | 151 | a0001c0001t0001g0265 a0001c0001t0002g0200 a0001c0001t0003g0032 others(148): Show |
158 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(155): Show |
intron_variant | MODIFIER | c.450+856A>G | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 2/3 | chr2 | 232663805 | |||||||
| chr2:232663877 | T | G | 62 | a0001c0001t0001g0308 a0001c0001t0002g0013 a0001c0001t0002g0117 others(59): Show |
62 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(59): Show |
intron_variant | MODIFIER | c.450+928T>G | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 2/3 | chr2 | 232663877 | |||||||
| chr2:232664182 | A | G | 1 | a0001c0001t0002g0246 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.450+1233A>G | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 2/3 | chr2 | 232664182 | |||||||
| chr2:232664248 | C | T | 76 | a0001c0001t0002g0200 a0001c0001t0003g0032 a0001c0001t0003g0037 others(73): Show |
83 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.450+1299C>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 2/3 | chr2 | 232664248 | |||||||
| chr2:232664258 | C | T | 1 | a0001c0001t0002g0258 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.450+1309C>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 2/3 | chr2 | 232664258 | |||||||
| chr2:232664420 | T | C | 1 | a0003c0005t0011g0023 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.450+1471T>C | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 2/3 | chr2 | 232664420 | |||||||
| chr2:232664458 | A | T | 2 | a0001c0001t0003g0242 a0001c0001t0003g0247 |
2 | HG01081.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.450+1509A>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 2/3 | chr2 | 232664458 | |||||||
| chr2:232664606 | G | GT | 76 | a0001c0001t0001g0048 a0001c0001t0001g0050 a0001c0001t0001g0315 others(73): Show |
76 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.450+1682dupT | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 232664606 | ||||||
| chr2:232664606 | G | GTT | 15 | a0001c0001t0001g0049 a0001c0001t0001g0051 a0001c0001t0001g0052 others(12): Show |
15 | HG00438.hp2 HG00544.hp2 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.450+1681_450+1682d others(4): Show |
EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 232664606 | ||||||
| chr2:232664606 | GT | G | 128 | a0001c0001t0001g0024 a0001c0001t0001g0036 a0001c0001t0001g0077 others(125): Show |
131 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.450+1682delT | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 232664606 | ||||||
| chr2:232664606 | GTT | G | 26 | a0001c0001t0001g0019 a0001c0001t0001g0172 a0001c0001t0002g0349 others(23): Show |
27 | HG01109.hp2 HG01261.hp1 HG01891.hp1 others(24): Show |
intron_variant | MODIFIER | c.450+1681_450+1682d others(4): Show |
EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 232664606 | ||||||
| chr2:232664628 | T | C | 1 | a0002c0002t0001g0229 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.450+1679T>C | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 2/3 | chr2 | 232664628 | |||||||
| chr2:232664645 | G | A | 1 | a0002c0002t0022g0263 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.450+1696G>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 2/3 | chr2 | 232664645 | |||||||
| chr2:232664703 | T | C | 1 | a0001c0001t0002g0117 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.450+1754T>C | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 2/3 | chr2 | 232664703 | |||||||
| chr2:232664723 | C | A | 155 | a0001c0001t0001g0265 a0001c0001t0002g0200 a0001c0001t0003g0032 others(152): Show |
162 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(159): Show |
intron_variant | MODIFIER | c.450+1774C>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 2/3 | chr2 | 232664723 | |||||||
| chr2:232664895 | G | A | 1 | a0001c0001t0003g0256 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.450+1946G>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 2/3 | chr2 | 232664895 | |||||||
| chr2:232665151 | G | A | 1 | a0001c0001t0005g0300 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.450+2202G>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 2/3 | chr2 | 232665151 | |||||||
| chr2:232665190 | T | G | 214 | a0001c0001t0001g0019 a0001c0001t0001g0048 a0001c0001t0001g0049 others(211): Show |
222 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(219): Show |
intron_variant | MODIFIER | c.450+2241T>G | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 2/3 | chr2 | 232665190 | |||||||
| chr2:232665199 | G | A | 1 | a0002c0003t0001g0148 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.450+2250G>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 2/3 | chr2 | 232665199 | |||||||
| chr2:232665424 | T | C | 6 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(3): Show |
6 | HG00544.hp2 HG02083.hp2 HG02293.hp2 others(3): Show |
intron_variant | MODIFIER | c.450+2475T>C | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 2/3 | chr2 | 232665424 | |||||||
| chr2:232665427 | CT | C | 7 | a0001c0001t0003g0241 a0001c0001t0006g0079 a0001c0001t0008g0283 others(4): Show |
7 | HG01099.hp1 HG01243.hp1 HG01517.hp1 others(4): Show |
intron_variant | MODIFIER | c.450+2490delT | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 232665427 | ||||||
| chr2:232665641 | T | C | 319 | a0001c0001t0001g0012 a0001c0001t0001g0019 a0001c0001t0001g0024 others(316): Show |
330 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(327): Show |
intron_variant | MODIFIER | c.450+2692T>C | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 2/3 | chr2 | 232665641 | |||||||
| chr2:232665664 | C | T | 1 | a0001c0001t0004g0178 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.450+2715C>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 2/3 | chr2 | 232665664 | |||||||
| chr2:232665812 | G | A | 1 | a0001c0001t0004g0031 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.450+2863G>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 2/3 | chr2 | 232665812 | |||||||
| chr2:232665835 | C | G | 2 | a0001c0004t0003g0186 a0001c0004t0003g0188 |
2 | NA18944.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.450+2886C>G | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 2/3 | chr2 | 232665835 | |||||||
| chr2:232665860 | T | C | 229 | a0001c0001t0001g0019 a0001c0001t0001g0048 a0001c0001t0001g0049 others(226): Show |
239 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(236): Show |
intron_variant | MODIFIER | c.450+2911T>C | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 2/3 | chr2 | 232665860 | |||||||
| chr2:232665889 | A | G | 1 | a0001c0001t0013g0039 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.450+2940A>G | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 2/3 | chr2 | 232665889 | |||||||
| chr2:232665926 | A | G | 1 | a0001c0004t0001g0167 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.450+2977A>G | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 2/3 | chr2 | 232665926 | |||||||
| chr2:232666179 | C | T | 6 | a0001c0001t0005g0364 a0001c0006t0001g0034 a0001c0006t0001g0267 others(3): Show |
6 | HG01891.hp2 HG02965.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.450+3230C>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 2/3 | chr2 | 232666179 | |||||||
| chr2:232666276 | G | A | 1 | a0003c0005t0011g0023 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.450+3327G>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 2/3 | chr2 | 232666276 | |||||||
| chr2:232666393 | A | T | 7 | a0001c0001t0001g0033 a0001c0001t0005g0010 a0001c0001t0005g0281 others(4): Show |
8 | HG02055.hp1 HG02615.hp2 HG03453.hp1 others(5): Show |
intron_variant | MODIFIER | c.450+3444A>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 2/3 | chr2 | 232666393 | |||||||
| chr2:232666524 | C | T | 140 | a0001c0001t0002g0200 a0001c0001t0004g0031 a0001c0001t0010g0298 others(137): Show |
147 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.450+3575C>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 2/3 | chr2 | 232666524 | |||||||
| chr2:232666677 | C | T | 1 | a0001c0001t0002g0013 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.450+3728C>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 2/3 | chr2 | 232666677 | |||||||
| chr2:232666842 | T | C | 32 | a0001c0001t0004g0159 a0001c0001t0004g0177 a0001c0001t0004g0178 others(29): Show |
32 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(29): Show |
intron_variant | MODIFIER | c.450+3893T>C | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 2/3 | chr2 | 232666842 | |||||||
| chr2:232666854 | C | T | 32 | a0001c0001t0004g0159 a0001c0001t0004g0177 a0001c0001t0004g0178 others(29): Show |
32 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(29): Show |
intron_variant | MODIFIER | c.450+3905C>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 2/3 | chr2 | 232666854 | |||||||
| chr2:232666893 | A | G | 1 | a0001c0011t0003g0043 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.450+3944A>G | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 2/3 | chr2 | 232666893 | |||||||
| chr2:232666934 | G | A | 2 | a0001c0001t0006g0277 a0001c0001t0006g0278 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.450+3985G>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 2/3 | chr2 | 232666934 | |||||||
| chr2:232667010 | T | C | 6 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(3): Show |
6 | HG00544.hp2 HG02083.hp2 HG02293.hp2 others(3): Show |
intron_variant | MODIFIER | c.450+4061T>C | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 2/3 | chr2 | 232667010 | |||||||
| chr2:232667019 | C | G | 1 | a0002c0003t0001g0086 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.450+4070C>G | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 2/3 | chr2 | 232667019 | |||||||
| chr2:232667182 | A | G | 2 | a0002c0002t0001g0314 a0002c0003t0001g0163 |
2 | HG00544.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.450+4233A>G | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 2/3 | chr2 | 232667182 | |||||||
| chr2:232667288 | C | T | 2 | a0002c0002t0001g0204 a0002c0002t0001g0206 |
2 | HG02056.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.450+4339C>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 2/3 | chr2 | 232667288 | |||||||
| chr2:232667525 | T | TTTAA | 11 | a0001c0001t0003g0032 a0001c0001t0003g0037 a0001c0001t0003g0266 others(8): Show |
11 | HG02145.hp2 HG02572.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.450+4591_450+4594d others(6): Show |
EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 232667525 | ||||||
| chr2:232667540 | A | AATTT | 6 | a0001c0001t0003g0237 a0001c0001t0003g0357 a0001c0001t0007g0002 others(3): Show |
8 | HG01884.hp2 HG02145.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.450+4616_450+4619d others(6): Show |
EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 232667540 | ||||||
| chr2:232667540 | A | T | 25 | a0001c0001t0001g0048 a0001c0001t0002g0334 a0001c0001t0002g0349 others(22): Show |
29 | HG00323.hp2 HG01074.hp1 HG01081.hp2 others(26): Show |
intron_variant | MODIFIER | c.450+4591A>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 2/3 | chr2 | 232667540 | |||||||
| chr2:232667544 | T | A | 182 | a0001c0001t0001g0012 a0001c0001t0001g0019 a0001c0001t0001g0024 others(179): Show |
186 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.450+4595T>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 2/3 | chr2 | 232667544 | |||||||
| chr2:232667548 | T | A | 50 | a0001c0001t0001g0012 a0001c0001t0001g0024 a0001c0001t0001g0036 others(47): Show |
51 | HG00438.hp1 HG00597.hp1 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.450+4599T>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 2/3 | chr2 | 232667548 | |||||||
| chr2:232667552 | T | A | 11 | a0001c0001t0001g0012 a0001c0001t0001g0036 a0001c0001t0001g0077 others(8): Show |
11 | HG01099.hp1 HG01106.hp2 HG01346.hp1 others(8): Show |
intron_variant | MODIFIER | c.450+4603T>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 2/3 | chr2 | 232667552 | |||||||
| chr2:232667609 | A | G | 1 | a0001c0001t0013g0039 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.450+4660A>G | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 2/3 | chr2 | 232667609 | |||||||
| chr2:232667713 | C | T | 37 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(34): Show |
37 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(34): Show |
intron_variant | MODIFIER | c.451-4596C>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 2/3 | chr2 | 232667713 | |||||||
| chr2:232667857 | G | C | 303 | a0001c0001t0001g0012 a0001c0001t0001g0024 a0001c0001t0001g0033 others(300): Show |
312 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(309): Show |
intron_variant | MODIFIER | c.451-4452G>C | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 2/3 | chr2 | 232667857 | |||||||
| chr2:232668107 | T | C | 1 | a0001c0001t0003g0234 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.451-4202T>C | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 2/3 | chr2 | 232668107 | |||||||
| chr2:232668152 | C | T | 5 | a0002c0003t0001g0193 a0002c0003t0001g0196 a0002c0003t0001g0209 others(2): Show |
5 | HG02135.hp1 NA18962.hp1 NA18970.hp2 others(2): Show |
intron_variant | MODIFIER | c.451-4157C>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 2/3 | chr2 | 232668152 | |||||||
| chr2:232668394 | C | T | 3 | a0001c0001t0001g0024 a0001c0001t0001g0172 a0001c0001t0001g0356 |
3 | HG03041.hp1 HG03579.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.451-3915C>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 2/3 | chr2 | 232668394 | |||||||
| chr2:232668492 | C | T | 57 | a0001c0001t0001g0012 a0001c0001t0001g0024 a0001c0001t0001g0033 others(54): Show |
59 | HG01106.hp2 HG01109.hp2 HG01243.hp1 others(56): Show |
intron_variant | MODIFIER | c.451-3817C>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 2/3 | chr2 | 232668492 | |||||||
| chr2:232668549 | G | A | 1 | a0002c0003t0001g0149 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.451-3760G>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 2/3 | chr2 | 232668549 | |||||||
| chr2:232668581 | G | C | 1 | a0001c0004t0001g0167 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.451-3728G>C | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 2/3 | chr2 | 232668581 | |||||||
| chr2:232668619 | T | C | 8 | a0001c0001t0003g0056 a0001c0001t0003g0245 a0001c0001t0003g0335 others(5): Show |
8 | HG00609.hp2 HG01361.hp2 HG01993.hp2 others(5): Show |
intron_variant | MODIFIER | c.451-3690T>C | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 2/3 | chr2 | 232668619 | |||||||
| chr2:232668620 | G | A | 1 | a0002c0002t0001g0144 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.451-3689G>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 2/3 | chr2 | 232668620 | |||||||
| chr2:232668683 | G | A | 6 | a0001c0001t0004g0031 a0001c0001t0005g0364 a0001c0006t0001g0034 others(3): Show |
6 | HG01891.hp2 HG02615.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.451-3626G>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 2/3 | chr2 | 232668683 | |||||||
| chr2:232668756 | C | T | 25 | a0001c0001t0001g0308 a0001c0001t0006g0025 a0001c0001t0006g0026 others(22): Show |
26 | HG01109.hp2 HG01243.hp1 HG01891.hp1 others(23): Show |
intron_variant | MODIFIER | c.451-3553C>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 2/3 | chr2 | 232668756 | |||||||
| chr2:232668821 | A | G | 144 | a0001c0001t0005g0300 a0001c0001t0005g0303 a0001c0009t0005g0299 others(141): Show |
151 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.451-3488A>G | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 2/3 | chr2 | 232668821 | |||||||
| chr2:232668876 | C | T | 1 | a0002c0002t0001g0045 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.451-3433C>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 2/3 | chr2 | 232668876 | |||||||
| chr2:232668904 | G | T | 2 | a0002c0002t0005g0292 a0002c0003t0001g0120 |
2 | HG01884.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.451-3405G>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 2/3 | chr2 | 232668904 | |||||||
| chr2:232669116 | G | A | 1 | a0001c0004t0004g0104 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.451-3193G>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 2/3 | chr2 | 232669116 | |||||||
| chr2:232669139 | G | T | 1 | a0001c0001t0013g0039 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.451-3170G>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 2/3 | chr2 | 232669139 | |||||||
| chr2:232669187 | T | C | 1 | a0002c0003t0001g0125 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.451-3122T>C | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 2/3 | chr2 | 232669187 | |||||||
| chr2:232669243 | T | G | 1 | a0002c0002t0001g0044 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.451-3066T>G | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 2/3 | chr2 | 232669243 | |||||||
| chr2:232669262 | C | T | 1 | a0001c0001t0002g0142 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.451-3047C>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 2/3 | chr2 | 232669262 | |||||||
| chr2:232669383 | G | A | 2 | a0001c0004t0004g0207 a0001c0004t0004g0208 |
2 | NA18969.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.451-2926G>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 2/3 | chr2 | 232669383 | |||||||
| chr2:232669602 | C | CT | 139 | a0001c0001t0003g0008 a0001c0001t0003g0037 a0001c0001t0003g0235 others(136): Show |
146 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.451-2690dupT | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 232669602 | ||||||
| chr2:232669602 | C | CTT | 8 | a0002c0002t0001g0144 a0002c0002t0001g0201 a0002c0002t0001g0255 others(5): Show |
9 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(6): Show |
intron_variant | MODIFIER | c.451-2691_451-2690d others(4): Show |
EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 232669602 | ||||||
| chr2:232669602 | CT | C | 32 | a0001c0001t0002g0200 a0001c0001t0004g0159 a0001c0001t0004g0177 others(29): Show |
32 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(29): Show |
intron_variant | MODIFIER | c.451-2690delT | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 232669602 | ||||||
| chr2:232669607 | T | C | 2 | a0001c0001t0001g0024 a0001c0001t0001g0356 |
2 | HG03579.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.451-2702T>C | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 2/3 | chr2 | 232669607 | |||||||
| chr2:232669657 | A | G | 1 | a0001c0009t0005g0299 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.451-2652A>G | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 2/3 | chr2 | 232669657 | |||||||
| chr2:232669688 | C | T | 6 | a0001c0001t0001g0024 a0001c0001t0001g0172 a0001c0001t0001g0356 others(3): Show |
6 | HG02723.hp1 HG03041.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.451-2621C>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 2/3 | chr2 | 232669688 | |||||||
| chr2:232669897 | C | T | 1 | a0001c0004t0003g0094 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.451-2412C>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 2/3 | chr2 | 232669897 | |||||||
| chr2:232669966 | G | A | 136 | a0002c0002t0001g0001 a0002c0002t0001g0011 a0002c0002t0001g0040 others(133): Show |
143 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.451-2343G>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 2/3 | chr2 | 232669966 | |||||||
| chr2:232669968 | A | G | 2 | a0001c0001t0002g0334 a0001c0001t0002g0349 |
2 | NA19074.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.451-2341A>G | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 2/3 | chr2 | 232669968 | |||||||
| chr2:232670102 | T | A | 2 | a0002c0003t0001g0112 a0002c0003t0014g0116 |
2 | HG03831.hp2 NA18941.hp2 |
intron_variant | MODIFIER | c.451-2207T>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 2/3 | chr2 | 232670102 | |||||||
| chr2:232670305 | A | G | 32 | a0001c0001t0004g0159 a0001c0001t0004g0177 a0001c0001t0004g0178 others(29): Show |
32 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(29): Show |
intron_variant | MODIFIER | c.451-2004A>G | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 2/3 | chr2 | 232670305 | |||||||
| chr2:232670346 | C | T | 31 | a0001c0001t0004g0159 a0001c0001t0004g0177 a0001c0001t0004g0178 others(28): Show |
31 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(28): Show |
intron_variant | MODIFIER | c.451-1963C>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 2/3 | chr2 | 232670346 | |||||||
| chr2:232670362 | A | G | 1 | a0001c0004t0004g0168 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.451-1947A>G | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 2/3 | chr2 | 232670362 | |||||||
| chr2:232670440 | CA | C | 50 | a0001c0001t0001g0012 a0001c0001t0001g0033 a0001c0001t0001g0036 others(47): Show |
51 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.451-1858delA | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 232670440 | ||||||
| chr2:232670571 | A | G | 1 | a0001c0004t0002g0130 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.451-1738A>G | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 2/3 | chr2 | 232670571 | |||||||
| chr2:232670576 | C | T | 31 | a0001c0001t0004g0159 a0001c0001t0004g0177 a0001c0001t0004g0178 others(28): Show |
31 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(28): Show |
intron_variant | MODIFIER | c.451-1733C>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 2/3 | chr2 | 232670576 | |||||||
| chr2:232670661 | T | TA | 137 | a0002c0002t0001g0001 a0002c0002t0001g0011 a0002c0002t0001g0040 others(134): Show |
144 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.451-1637dupA | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 232670661 | ||||||
| chr2:232670661 | TA | T | 10 | a0001c0001t0001g0052 a0001c0001t0002g0326 a0001c0001t0002g0332 others(7): Show |
10 | HG01891.hp2 HG02293.hp2 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.451-1637delA | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 232670661 | ||||||
| chr2:232670875 | G | A | 31 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(28): Show |
32 | HG00544.hp2 HG01109.hp2 HG01243.hp1 others(29): Show |
intron_variant | MODIFIER | c.451-1434G>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 2/3 | chr2 | 232670875 | |||||||
| chr2:232671418 | C | A | 1 | a0001c0004t0002g0225 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.451-891C>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 2/3 | chr2 | 232671418 | |||||||
| chr2:232671500 | C | T | 1 | a0002c0003t0001g0070 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.451-809C>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 2/3 | chr2 | 232671500 | |||||||
| chr2:232671666 | G | T | 1 | a0001c0001t0013g0039 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.451-643G>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 2/3 | chr2 | 232671666 | |||||||
| chr2:232671823 | G | A | 1 | a0002c0003t0001g0109 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.451-486G>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 2/3 | chr2 | 232671823 | |||||||
| chr2:232671913 | C | T | 33 | a0001c0001t0004g0159 a0001c0001t0004g0177 a0001c0001t0004g0178 others(30): Show |
33 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(30): Show |
intron_variant | MODIFIER | c.451-396C>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 2/3 | chr2 | 232671913 | |||||||
| chr2:232672005 | G | A | 1 | a0002c0002t0001g0363 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.451-304G>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 2/3 | chr2 | 232672005 | |||||||
| chr2:232672055 | C | CA | 9 | a0001c0001t0001g0033 a0001c0001t0004g0344 a0001c0001t0005g0010 others(6): Show |
10 | HG01433.hp2 HG02055.hp1 HG02056.hp1 others(7): Show |
intron_variant | MODIFIER | c.451-239dupA | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 232672055 | ||||||
| chr2:232672090 | C | G | 1 | a0001c0001t0001g0024 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.451-219C>G | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 2/3 | chr2 | 232672090 | |||||||
| chr2:232672140 | G | T | 1 | a0001c0001t0001g0019 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.451-169G>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 2/3 | chr2 | 232672140 | |||||||
| chr2:232672160 | A | G | 1 | a0001c0001t0013g0039 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.451-149A>G | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 2/3 | chr2 | 232672160 | |||||||
| chr2:232672216 | T | C | 142 | a0002c0002t0001g0001 a0002c0002t0001g0011 a0002c0002t0001g0040 others(139): Show |
149 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(146): Show |
intron_variant | MODIFIER | c.451-93T>C | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 2/3 | chr2 | 232672216 | |||||||
| chr2:232672767 | A | G | 286 | a0001c0001t0001g0012 a0001c0001t0001g0033 a0001c0001t0001g0036 others(283): Show |
295 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(292): Show |
intron_variant | MODIFIER | c.585+324A>G | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | chr2 | 232672767 | |||||||
| chr2:232672873 | C | T | 7 | a0001c0001t0004g0031 a0001c0001t0005g0364 a0001c0006t0001g0034 others(4): Show |
7 | HG01891.hp2 HG02615.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.585+430C>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | chr2 | 232672873 | |||||||
| chr2:232673004 | G | A | 57 | a0001c0001t0002g0013 a0001c0001t0002g0117 a0001c0001t0002g0118 others(54): Show |
57 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(54): Show |
intron_variant | MODIFIER | c.585+561G>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | chr2 | 232673004 | |||||||
| chr2:232673103 | C | T | 8 | a0001c0001t0001g0024 a0001c0001t0001g0172 a0001c0001t0001g0356 others(5): Show |
9 | HG01261.hp1 HG02451.hp1 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.585+660C>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | chr2 | 232673103 | |||||||
| chr2:232673374 | G | C | 3 | a0002c0002t0001g0175 a0002c0002t0001g0180 a0002c0002t0001g0229 |
3 | HG00099.hp1 HG01261.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.585+931G>C | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | chr2 | 232673374 | |||||||
| chr2:232673590 | T | C | 59 | a0001c0001t0002g0013 a0001c0001t0002g0117 a0001c0001t0002g0118 others(56): Show |
59 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.585+1147T>C | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | chr2 | 232673590 | |||||||
| chr2:232673682 | G | T | 32 | a0001c0001t0004g0159 a0001c0001t0004g0177 a0001c0001t0004g0178 others(29): Show |
32 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(29): Show |
intron_variant | MODIFIER | c.585+1239G>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | chr2 | 232673682 | |||||||
| chr2:232673766 | C | T | 7 | a0001c0001t0004g0031 a0001c0001t0005g0364 a0001c0006t0001g0034 others(4): Show |
7 | HG01891.hp2 HG02615.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.585+1323C>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | chr2 | 232673766 | |||||||
| chr2:232673907 | C | CT | 85 | a0001c0001t0002g0013 a0001c0001t0002g0117 a0001c0001t0002g0118 others(82): Show |
85 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.585+1483dupT | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr2 | 232673907 | ||||||
| chr2:232673907 | CT | C | 6 | a0001c0001t0001g0036 a0001c0004t0001g0157 a0001c0004t0003g0111 others(3): Show |
6 | HG01884.hp1 HG02258.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.585+1483delT | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr2 | 232673907 | ||||||
| chr2:232673977 | T | C | 37 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(34): Show |
37 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(34): Show |
intron_variant | MODIFIER | c.585+1534T>C | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | chr2 | 232673977 | |||||||
| chr2:232674033 | T | C | 25 | a0001c0001t0001g0308 a0001c0001t0006g0025 a0001c0001t0006g0026 others(22): Show |
26 | HG01109.hp2 HG01243.hp1 HG01891.hp1 others(23): Show |
intron_variant | MODIFIER | c.585+1590T>C | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | chr2 | 232674033 | |||||||
| chr2:232674065 | C | T | 37 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(34): Show |
37 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(34): Show |
intron_variant | MODIFIER | c.585+1622C>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | chr2 | 232674065 | |||||||
| chr2:232674109 | A | G | 17 | a0001c0001t0001g0012 a0001c0001t0001g0033 a0001c0001t0001g0036 others(14): Show |
18 | HG01106.hp2 HG01346.hp1 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.585+1666A>G | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | chr2 | 232674109 | |||||||
| chr2:232674158 | C | T | 37 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(34): Show |
37 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(34): Show |
intron_variant | MODIFIER | c.585+1715C>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | chr2 | 232674158 | |||||||
| chr2:232674301 | T | G | 7 | a0001c0001t0004g0031 a0001c0001t0005g0364 a0001c0006t0001g0034 others(4): Show |
7 | HG01891.hp2 HG02615.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.585+1858T>G | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | chr2 | 232674301 | |||||||
| chr2:232674373 | C | T | 1 | a0002c0002t0001g0280 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.585+1930C>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | chr2 | 232674373 | |||||||
| chr2:232674523 | C | T | 6 | a0001c0001t0001g0024 a0001c0001t0001g0172 a0001c0001t0001g0356 others(3): Show |
6 | HG02723.hp1 HG03041.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.585+2080C>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | chr2 | 232674523 | |||||||
| chr2:232674830 | G | A | 1 | a0001c0001t0013g0039 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.585+2387G>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | chr2 | 232674830 | |||||||
| chr2:232674870 | A | G | 32 | a0001c0001t0004g0159 a0001c0001t0004g0177 a0001c0001t0004g0178 others(29): Show |
32 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(29): Show |
intron_variant | MODIFIER | c.585+2427A>G | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | chr2 | 232674870 | |||||||
| chr2:232674955 | A | C | 1 | a0001c0001t0021g0272 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.585+2512A>C | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | chr2 | 232674955 | |||||||
| chr2:232675118 | G | A | 31 | a0001c0001t0004g0159 a0001c0001t0004g0177 a0001c0001t0004g0178 others(28): Show |
31 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(28): Show |
intron_variant | MODIFIER | c.585+2675G>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | chr2 | 232675118 | |||||||
| chr2:232675180 | G | A | 1 | a0002c0003t0001g0099 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.585+2737G>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | chr2 | 232675180 | |||||||
| chr2:232675187 | A | AAAAG | 297 | a0001c0001t0001g0012 a0001c0001t0001g0024 a0001c0001t0001g0033 others(294): Show |
306 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(303): Show |
intron_variant | MODIFIER | c.585+2745_585+2746i others(6): Show |
EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr2 | 232675187 | ||||||
| chr2:232675187 | A | G | 1 | a0002c0003t0001g0099 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.585+2744A>G | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | chr2 | 232675187 | |||||||
| chr2:232675203 | A | AAAGG | 60 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(57): Show |
61 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.585+2778_585+2781d others(6): Show |
EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr2 | 232675203 | ||||||
| chr2:232675246 | G | GAAAGA | 27 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0052 others(24): Show |
28 | HG00544.hp2 HG01109.hp2 HG01891.hp1 others(25): Show |
intron_variant | MODIFIER | c.585+2826_585+2830d others(7): Show |
EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr2 | 232675246 | ||||||
| chr2:232675246 | G | GAAAGAAA others(3): Show |
1 | a0001c0001t0008g0294 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.585+2821_585+2830d others(12): Show |
EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr2 | 232675246 | ||||||
| chr2:232675246 | GAAAGA | G | 171 | a0001c0001t0002g0252 a0001c0001t0003g0242 a0001c0001t0004g0159 others(168): Show |
178 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(175): Show |
intron_variant | MODIFIER | c.585+2826_585+2830d others(7): Show |
EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr2 | 232675246 | ||||||
| chr2:232675556 | C | T | 6 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(3): Show |
6 | HG00544.hp2 HG02083.hp2 HG02293.hp2 others(3): Show |
intron_variant | MODIFIER | c.585+3113C>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | chr2 | 232675556 | |||||||
| chr2:232675664 | G | T | 31 | a0001c0001t0004g0159 a0001c0001t0004g0177 a0001c0001t0004g0178 others(28): Show |
31 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(28): Show |
intron_variant | MODIFIER | c.585+3221G>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | chr2 | 232675664 | |||||||
| chr2:232675887 | C | A | 3 | a0001c0001t0020g0276 a0001c0004t0004g0164 a0001c0004t0004g0165 |
3 | HG03041.hp2 HG03098.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.585+3444C>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | chr2 | 232675887 | |||||||
| chr2:232675899 | A | G | 1 | a0001c0001t0001g0308 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.585+3456A>G | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | chr2 | 232675899 | |||||||
| chr2:232676071 | G | C | 2 | a0001c0001t0010g0298 a0001c0004t0002g0262 |
2 | HG03098.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.585+3628G>C | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | chr2 | 232676071 | |||||||
| chr2:232676103 | A | G | 31 | a0001c0001t0004g0159 a0001c0001t0004g0177 a0001c0001t0004g0178 others(28): Show |
31 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(28): Show |
intron_variant | MODIFIER | c.585+3660A>G | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | chr2 | 232676103 | |||||||
| chr2:232676145 | A | C | 1 | a0002c0003t0001g0101 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.585+3702A>C | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | chr2 | 232676145 | |||||||
| chr2:232676153 | C | T | 6 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(3): Show |
6 | HG00544.hp2 HG02083.hp2 HG02293.hp2 others(3): Show |
intron_variant | MODIFIER | c.585+3710C>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | chr2 | 232676153 | |||||||
| chr2:232676166 | C | T | 1 | a0003c0005t0002g0015 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.585+3723C>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | chr2 | 232676166 | |||||||
| chr2:232676199 | C | T | 238 | a0001c0001t0001g0012 a0001c0001t0001g0024 a0001c0001t0001g0033 others(235): Show |
247 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(244): Show |
intron_variant | MODIFIER | c.585+3756C>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | chr2 | 232676199 | |||||||
| chr2:232676283 | G | C | 7 | a0001c0001t0004g0031 a0001c0001t0005g0364 a0001c0006t0001g0034 others(4): Show |
7 | HG01891.hp2 HG02615.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.585+3840G>C | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | chr2 | 232676283 | |||||||
| chr2:232676366 | G | A | 31 | a0001c0001t0004g0159 a0001c0001t0004g0177 a0001c0001t0004g0178 others(28): Show |
31 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(28): Show |
intron_variant | MODIFIER | c.585+3923G>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | chr2 | 232676366 | |||||||
| chr2:232676407 | C | T | 1 | a0001c0001t0013g0039 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.585+3964C>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | chr2 | 232676407 | |||||||
| chr2:232676408 | G | A | 2 | a0001c0004t0001g0057 a0003c0005t0001g0029 |
2 | HG01099.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.585+3965G>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | chr2 | 232676408 | |||||||
| chr2:232676501 | A | G | 6 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(3): Show |
6 | HG00544.hp2 HG02083.hp2 HG02293.hp2 others(3): Show |
intron_variant | MODIFIER | c.585+4058A>G | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | chr2 | 232676501 | |||||||
| chr2:232676524 | C | T | 1 | a0001c0001t0002g0222 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.585+4081C>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | chr2 | 232676524 | |||||||
| chr2:232676525 | G | A | 31 | a0001c0001t0004g0159 a0001c0001t0004g0177 a0001c0001t0004g0178 others(28): Show |
31 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(28): Show |
intron_variant | MODIFIER | c.585+4082G>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | chr2 | 232676525 | |||||||
| chr2:232676545 | G | A | 321 | a0001c0001t0001g0012 a0001c0001t0001g0019 a0001c0001t0001g0024 others(318): Show |
332 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(329): Show |
intron_variant | MODIFIER | c.585+4102G>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | chr2 | 232676545 | |||||||
| chr2:232676685 | A | C | 2 | a0001c0001t0013g0039 a0001c0004t0001g0167 |
2 | HG03195.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.585+4242A>C | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | chr2 | 232676685 | |||||||
| chr2:232676842 | A | G | 5 | a0001c0001t0006g0097 a0001c0001t0008g0294 a0001c0001t0021g0272 others(2): Show |
5 | HG02630.hp1 HG02922.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.585+4399A>G | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | chr2 | 232676842 | |||||||
| chr2:232676914 | T | G | 9 | a0001c0001t0006g0035 a0001c0001t0006g0097 a0001c0001t0006g0098 others(6): Show |
9 | HG01109.hp2 HG02258.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.585+4471T>G | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | chr2 | 232676914 | |||||||
| chr2:232676952 | A | G | 1 | a0001c0004t0001g0221 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.585+4509A>G | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | chr2 | 232676952 | |||||||
| chr2:232676985 | G | A | 2 | a0001c0001t0001g0019 a0001c0001t0001g0265 |
2 | HG03540.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.585+4542G>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | chr2 | 232676985 | |||||||
| chr2:232677000 | TAAAACAA others(3): Show |
T | 15 | a0001c0001t0001g0012 a0001c0001t0001g0033 a0001c0001t0001g0036 others(12): Show |
16 | HG01106.hp2 HG01346.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.586-4570_586-4561d others(12): Show |
EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr2 | 232677000 | ||||||
| chr2:232677015 | C | T | 1 | a0002c0002t0001g0143 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.586-4570C>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | chr2 | 232677015 | |||||||
| chr2:232677075 | C | A | 1 | a0001c0001t0003g0235 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.586-4510C>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | chr2 | 232677075 | |||||||
| chr2:232677081 | A | G | 40 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(37): Show |
40 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(37): Show |
intron_variant | MODIFIER | c.586-4504A>G | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | chr2 | 232677081 | |||||||
| chr2:232677207 | T | TAC | 37 | a0001c0001t0001g0012 a0001c0001t0001g0024 a0001c0001t0001g0033 others(34): Show |
40 | HG00280.hp1 HG00733.hp1 HG01106.hp2 others(37): Show |
intron_variant | MODIFIER | c.586-4345_586-4344d others(4): Show |
EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr2 | 232677207 | ||||||
| chr2:232677207 | T | TACAC | 52 | a0001c0001t0002g0013 a0001c0001t0002g0117 a0001c0001t0002g0118 others(49): Show |
52 | HG00423.hp1 HG00558.hp1 HG00621.hp1 others(49): Show |
intron_variant | MODIFIER | c.586-4347_586-4344d others(6): Show |
EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr2 | 232677207 | ||||||
| chr2:232677207 | T | TACACAC | 24 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(21): Show |
24 | HG00140.hp2 HG00544.hp2 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.586-4349_586-4344d others(8): Show |
EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr2 | 232677207 | ||||||
| chr2:232677207 | T | TACACACA others(1): Show |
5 | a0001c0001t0001g0308 a0001c0001t0006g0269 a0001c0004t0002g0016 others(2): Show |
5 | HG02572.hp2 HG02818.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.586-4351_586-4344d others(10): Show |
EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr2 | 232677207 | ||||||
| chr2:232677207 | T | TACACACA others(3): Show |
9 | a0001c0001t0006g0025 a0001c0001t0006g0026 a0001c0001t0006g0030 others(6): Show |
10 | HG01243.hp1 HG02280.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.586-4353_586-4344d others(12): Show |
EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr2 | 232677207 | ||||||
| chr2:232677207 | T | TACACACA others(5): Show |
9 | a0001c0001t0006g0035 a0001c0001t0006g0079 a0001c0001t0006g0097 others(6): Show |
9 | HG01109.hp2 HG02630.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.586-4355_586-4344d others(14): Show |
EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr2 | 232677207 | ||||||
| chr2:232677207 | T | TACACACA others(7): Show |
6 | a0001c0001t0006g0098 a0001c0001t0020g0276 a0001c0004t0004g0103 others(3): Show |
6 | HG02258.hp2 HG02622.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.586-4357_586-4344d others(16): Show |
EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr2 | 232677207 | ||||||
| chr2:232677207 | T | TACACACA others(9): Show |
1 | a0001c0004t0004g0168 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.586-4359_586-4344d others(18): Show |
EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr2 | 232677207 | ||||||
| chr2:232677207 | T | TACACACA others(11): Show |
1 | a0001c0001t0004g0319 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.586-4361_586-4344d others(20): Show |
EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr2 | 232677207 | ||||||
| chr2:232677207 | T | TACACACA others(13): Show |
4 | a0001c0001t0004g0177 a0001c0001t0004g0329 a0001c0001t0004g0344 others(1): Show |
4 | HG02056.hp1 HG02129.hp1 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.586-4363_586-4344d others(22): Show |
EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr2 | 232677207 | ||||||
| chr2:232677207 | T | TACACACA others(15): Show |
2 | a0001c0001t0004g0320 a0001c0004t0004g0147 |
2 | NA18989.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.586-4365_586-4344d others(24): Show |
EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr2 | 232677207 | ||||||
| chr2:232677207 | T | TACACACA others(17): Show |
6 | a0001c0001t0004g0338 a0001c0004t0004g0064 a0001c0004t0004g0104 others(3): Show |
6 | HG00408.hp2 NA18942.hp2 NA18947.hp1 others(3): Show |
intron_variant | MODIFIER | c.586-4367_586-4344d others(26): Show |
EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr2 | 232677207 | ||||||
| chr2:232677207 | T | TACACACA others(19): Show |
7 | a0001c0001t0004g0353 a0001c0001t0004g0359 a0001c0001t0012g0351 others(4): Show |
7 | HG02523.hp1 HG02523.hp2 NA18747.hp2 others(4): Show |
intron_variant | MODIFIER | c.586-4369_586-4344d others(28): Show |
EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr2 | 232677207 | ||||||
| chr2:232677207 | T | TACACACA others(21): Show |
1 | a0001c0001t0004g0178 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.586-4371_586-4344d others(30): Show |
EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr2 | 232677207 | ||||||
| chr2:232677207 | T | TACACACA others(23): Show |
2 | a0001c0001t0004g0352 a0001c0004t0004g0146 |
2 | NA18981.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.586-4373_586-4344d others(32): Show |
EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr2 | 232677207 | ||||||
| chr2:232677207 | T | TACACACA others(25): Show |
1 | a0001c0001t0004g0159 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.586-4375_586-4344d others(34): Show |
EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr2 | 232677207 | ||||||
| chr2:232677207 | T | TACACACA others(27): Show |
1 | a0001c0004t0004g0171 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.586-4377_586-4344d others(36): Show |
EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr2 | 232677207 | ||||||
| chr2:232677207 | TAC | T | 5 | a0001c0001t0003g0007 a0001c0001t0003g0234 a0001c0001t0003g0242 others(2): Show |
6 | HG01070.hp2 HG01081.hp1 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.586-4345_586-4344d others(4): Show |
EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr2 | 232677207 | ||||||
| chr2:232677207 | TACACAC | T | 7 | a0002c0002t0001g0206 a0002c0002t0001g0342 a0002c0002t0005g0284 others(4): Show |
7 | HG01975.hp1 HG01981.hp1 HG02056.hp2 others(4): Show |
intron_variant | MODIFIER | c.586-4349_586-4344d others(8): Show |
EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr2 | 232677207 | ||||||
| chr2:232677207 | TACACACA others(1): Show |
T | 131 | a0002c0002t0001g0001 a0002c0002t0001g0011 a0002c0002t0001g0040 others(128): Show |
138 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.586-4351_586-4344d others(10): Show |
EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr2 | 232677207 | ||||||
| chr2:232677207 | TACACACA others(3): Show |
T | 9 | a0001c0001t0003g0056 a0001c0001t0003g0245 a0001c0001t0003g0335 others(6): Show |
9 | HG00609.hp2 HG01361.hp2 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.586-4353_586-4344d others(12): Show |
EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr2 | 232677207 | ||||||
| chr2:232677207 | TACACACA others(15): Show |
T | 1 | a0001c0001t0013g0039 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.586-4365_586-4344d others(24): Show |
EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr2 | 232677207 | ||||||
| chr2:232677210 | A | ACT | 13 | a0001c0004t0001g0223 a0001c0004t0003g0071 a0001c0004t0003g0082 others(10): Show |
13 | HG00609.hp1 HG02135.hp2 NA18939.hp2 others(10): Show |
intron_variant | MODIFIER | c.586-4374_586-4373i others(4): Show |
EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr2 | 232677210 | ||||||
| chr2:232677212 | A | T | 1 | a0001c0004t0003g0187 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.586-4373A>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | chr2 | 232677212 | |||||||
| chr2:232677222 | A | T | 7 | a0001c0001t0003g0056 a0001c0001t0003g0245 a0001c0001t0003g0335 others(4): Show |
7 | HG00609.hp2 HG01361.hp2 HG01993.hp2 others(4): Show |
intron_variant | MODIFIER | c.586-4363A>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | chr2 | 232677222 | |||||||
| chr2:232677242 | G | A | 32 | a0001c0001t0004g0159 a0001c0001t0004g0177 a0001c0001t0004g0178 others(29): Show |
32 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(29): Show |
intron_variant | MODIFIER | c.586-4343G>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | chr2 | 232677242 | |||||||
| chr2:232677243 | T | C | 31 | a0001c0001t0004g0159 a0001c0001t0004g0177 a0001c0001t0004g0178 others(28): Show |
31 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(28): Show |
intron_variant | MODIFIER | c.586-4342T>C | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | chr2 | 232677243 | |||||||
| chr2:232677264 | AACACACA others(3): Show |
A | 23 | a0001c0001t0001g0308 a0001c0001t0006g0025 a0001c0001t0006g0026 others(20): Show |
24 | HG01109.hp2 HG01243.hp1 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.586-4311_586-4302d others(12): Show |
EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr2 | 232677264 | ||||||
| chr2:232677264 | AACACACA others(5): Show |
A | 1 | a0001c0001t0006g0098 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.586-4311_586-4300d others(14): Show |
EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr2 | 232677264 | ||||||
| chr2:232677264 | AACACACA others(7): Show |
A | 1 | a0001c0001t0008g0287 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.586-4311_586-4298d others(16): Show |
EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr2 | 232677264 | ||||||
| chr2:232677266 | CACACACA others(1): Show |
C | 33 | a0001c0001t0004g0159 a0001c0001t0004g0177 a0001c0001t0004g0178 others(30): Show |
33 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(30): Show |
intron_variant | MODIFIER | c.586-4311_586-4304d others(10): Show |
EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr2 | 232677266 | ||||||
| chr2:232677270 | CACAT | C | 6 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(3): Show |
6 | HG00544.hp2 HG02083.hp2 HG02293.hp2 others(3): Show |
intron_variant | MODIFIER | c.586-4311_586-4308d others(6): Show |
EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr2 | 232677270 | ||||||
| chr2:232677274 | T | TAC | 45 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0014 others(42): Show |
47 | HG00099.hp2 HG00609.hp1 HG00609.hp2 others(44): Show |
intron_variant | MODIFIER | c.586-4292_586-4291d others(4): Show |
EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr2 | 232677274 | ||||||
| chr2:232677274 | TACAC | T | 232 | a0001c0001t0001g0012 a0001c0001t0001g0024 a0001c0001t0001g0033 others(229): Show |
240 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(237): Show |
intron_variant | MODIFIER | c.586-4294_586-4291d others(6): Show |
EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr2 | 232677274 | ||||||
| chr2:232677627 | T | C | 2 | a0001c0001t0010g0298 a0001c0004t0002g0262 |
2 | HG03098.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.586-3958T>C | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | chr2 | 232677627 | |||||||
| chr2:232677708 | G | C | 6 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(3): Show |
6 | HG00544.hp2 HG02083.hp2 HG02293.hp2 others(3): Show |
intron_variant | MODIFIER | c.586-3877G>C | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | chr2 | 232677708 | |||||||
| chr2:232677771 | C | G | 30 | a0001c0001t0004g0159 a0001c0001t0004g0177 a0001c0001t0004g0178 others(27): Show |
30 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(27): Show |
intron_variant | MODIFIER | c.586-3814C>G | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | chr2 | 232677771 | |||||||
| chr2:232677778 | A | G | 1 | a0001c0004t0004g0064 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.586-3807A>G | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | chr2 | 232677778 | |||||||
| chr2:232677798 | A | C | 31 | a0001c0001t0004g0159 a0001c0001t0004g0177 a0001c0001t0004g0178 others(28): Show |
31 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(28): Show |
intron_variant | MODIFIER | c.586-3787A>C | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | chr2 | 232677798 | |||||||
| chr2:232678151 | C | T | 2 | a0001c0001t0006g0079 a0001c0001t0008g0283 |
2 | HG01243.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.586-3434C>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | chr2 | 232678151 | |||||||
| chr2:232678152 | G | A | 32 | a0001c0001t0004g0159 a0001c0001t0004g0177 a0001c0001t0004g0178 others(29): Show |
32 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(29): Show |
intron_variant | MODIFIER | c.586-3433G>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | chr2 | 232678152 | |||||||
| chr2:232678271 | GA | G | 32 | a0001c0001t0004g0159 a0001c0001t0004g0177 a0001c0001t0004g0178 others(29): Show |
32 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(29): Show |
intron_variant | MODIFIER | c.586-3303delA | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr2 | 232678271 | ||||||
| chr2:232678300 | A | G | 1 | a0001c0001t0001g0036 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.586-3285A>G | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | chr2 | 232678300 | |||||||
| chr2:232678418 | G | C | 32 | a0001c0001t0004g0159 a0001c0001t0004g0177 a0001c0001t0004g0178 others(29): Show |
32 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(29): Show |
intron_variant | MODIFIER | c.586-3167G>C | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | chr2 | 232678418 | |||||||
| chr2:232678513 | G | A | 6 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(3): Show |
6 | HG00544.hp2 HG02083.hp2 HG02293.hp2 others(3): Show |
intron_variant | MODIFIER | c.586-3072G>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | chr2 | 232678513 | |||||||
| chr2:232678545 | G | A | 1 | a0001c0001t0005g0264 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.586-3040G>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | chr2 | 232678545 | |||||||
| chr2:232678627 | A | C | 86 | a0001c0001t0001g0012 a0001c0001t0001g0033 a0001c0001t0001g0036 others(83): Show |
87 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.586-2958A>C | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | chr2 | 232678627 | |||||||
| chr2:232678733 | T | A | 32 | a0001c0001t0004g0159 a0001c0001t0004g0177 a0001c0001t0004g0178 others(29): Show |
32 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(29): Show |
intron_variant | MODIFIER | c.586-2852T>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | chr2 | 232678733 | |||||||
| chr2:232678827 | C | T | 32 | a0001c0001t0004g0159 a0001c0001t0004g0177 a0001c0001t0004g0178 others(29): Show |
32 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(29): Show |
intron_variant | MODIFIER | c.586-2758C>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | chr2 | 232678827 | |||||||
| chr2:232678840 | G | A | 1 | a0001c0001t0021g0272 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.586-2745G>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | chr2 | 232678840 | |||||||
| chr2:232678972 | C | T | 32 | a0001c0001t0004g0159 a0001c0001t0004g0177 a0001c0001t0004g0178 others(29): Show |
32 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(29): Show |
intron_variant | MODIFIER | c.586-2613C>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | chr2 | 232678972 | |||||||
| chr2:232678979 | T | C | 32 | a0001c0001t0004g0159 a0001c0001t0004g0177 a0001c0001t0004g0178 others(29): Show |
32 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(29): Show |
intron_variant | MODIFIER | c.586-2606T>C | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | chr2 | 232678979 | |||||||
| chr2:232679179 | C | T | 7 | a0001c0001t0003g0119 a0001c0001t0003g0236 a0001c0001t0003g0248 others(4): Show |
7 | HG01070.hp1 HG01175.hp2 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.586-2406C>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | chr2 | 232679179 | |||||||
| chr2:232679182 | G | A | 70 | a0002c0002t0001g0001 a0002c0002t0001g0011 a0002c0002t0001g0040 others(67): Show |
77 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.586-2403G>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | chr2 | 232679182 | |||||||
| chr2:232679348 | C | T | 2 | a0002c0002t0001g0040 a0002c0002t0001g0213 |
2 | HG02698.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.586-2237C>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | chr2 | 232679348 | |||||||
| chr2:232679396 | CT | C | 33 | a0001c0001t0004g0159 a0001c0001t0004g0177 a0001c0001t0004g0178 others(30): Show |
33 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(30): Show |
intron_variant | MODIFIER | c.586-2179delT | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr2 | 232679396 | ||||||
| chr2:232679515 | C | G | 32 | a0001c0001t0004g0159 a0001c0001t0004g0177 a0001c0001t0004g0178 others(29): Show |
32 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(29): Show |
intron_variant | MODIFIER | c.586-2070C>G | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | chr2 | 232679515 | |||||||
| chr2:232679570 | G | A | 1 | a0001c0001t0010g0301 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.586-2015G>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | chr2 | 232679570 | |||||||
| chr2:232679588 | C | T | 72 | a0001c0001t0005g0264 a0002c0002t0001g0001 a0002c0002t0001g0011 others(69): Show |
79 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(76): Show |
intron_variant | MODIFIER | c.586-1997C>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | chr2 | 232679588 | |||||||
| chr2:232679646 | C | T | 3 | a0001c0001t0020g0276 a0001c0004t0004g0164 a0001c0004t0004g0165 |
3 | HG03041.hp2 HG03098.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.586-1939C>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | chr2 | 232679646 | |||||||
| chr2:232679712 | G | A | 5 | a0002c0002t0001g0316 a0002c0002t0001g0317 a0002c0002t0001g0358 others(2): Show |
5 | HG02027.hp2 NA18994.hp2 NA19010.hp2 others(2): Show |
intron_variant | MODIFIER | c.586-1873G>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | chr2 | 232679712 | |||||||
| chr2:232679717 | T | TA | 83 | a0001c0001t0001g0012 a0001c0001t0001g0033 a0001c0001t0001g0036 others(80): Show |
84 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.586-1851dupA | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr2 | 232679717 | ||||||
| chr2:232679717 | TA | T | 7 | a0001c0001t0005g0264 a0001c0001t0012g0351 a0001c0004t0002g0131 others(4): Show |
7 | HG03490.hp1 NA18747.hp2 NA18941.hp1 others(4): Show |
intron_variant | MODIFIER | c.586-1851delA | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr2 | 232679717 | ||||||
| chr2:232679752 | G | A | 32 | a0001c0001t0004g0159 a0001c0001t0004g0177 a0001c0001t0004g0178 others(29): Show |
32 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(29): Show |
intron_variant | MODIFIER | c.586-1833G>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | chr2 | 232679752 | |||||||
| chr2:232679754 | T | C | 32 | a0001c0001t0004g0159 a0001c0001t0004g0177 a0001c0001t0004g0178 others(29): Show |
32 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(29): Show |
intron_variant | MODIFIER | c.586-1831T>C | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | chr2 | 232679754 | |||||||
| chr2:232679777 | G | A | 3 | a0002c0003t0001g0193 a0002c0003t0001g0209 a0002c0003t0001g0212 |
3 | HG02135.hp1 NA18962.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.586-1808G>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | chr2 | 232679777 | |||||||
| chr2:232679801 | A | G | 1 | a0001c0001t0001g0265 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.586-1784A>G | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | chr2 | 232679801 | |||||||
| chr2:232680132 | A | C | 1 | a0001c0001t0003g0234 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.586-1453A>C | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | chr2 | 232680132 | |||||||
| chr2:232680232 | G | A | 2 | a0001c0001t0001g0019 a0001c0001t0001g0265 |
2 | HG03540.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.586-1353G>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | chr2 | 232680232 | |||||||
| chr2:232680252 | A | G | 124 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(121): Show |
125 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.586-1333A>G | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | chr2 | 232680252 | |||||||
| chr2:232680273 | TA | T | 26 | a0001c0001t0001g0308 a0001c0001t0006g0025 a0001c0001t0006g0026 others(23): Show |
27 | HG01109.hp2 HG01243.hp1 HG01891.hp1 others(24): Show |
intron_variant | MODIFIER | c.586-1300delA | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr2 | 232680273 | ||||||
| chr2:232680299 | G | A | 32 | a0001c0001t0004g0159 a0001c0001t0004g0177 a0001c0001t0004g0178 others(29): Show |
32 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(29): Show |
intron_variant | MODIFIER | c.586-1286G>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | chr2 | 232680299 | |||||||
| chr2:232680376 | C | CTGATA | 303 | a0001c0001t0001g0012 a0001c0001t0001g0019 a0001c0001t0001g0024 others(300): Show |
312 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(309): Show |
intron_variant | MODIFIER | c.586-1207_586-1203d others(7): Show |
EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr2 | 232680376 | ||||||
| chr2:232680462 | T | C | 32 | a0001c0001t0004g0159 a0001c0001t0004g0177 a0001c0001t0004g0178 others(29): Show |
32 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(29): Show |
intron_variant | MODIFIER | c.586-1123T>C | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | chr2 | 232680462 | |||||||
| chr2:232680496 | G | A | 1 | a0001c0001t0013g0039 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.586-1089G>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | chr2 | 232680496 | |||||||
| chr2:232680506 | G | A | 1 | a0001c0001t0003g0256 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.586-1079G>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | chr2 | 232680506 | |||||||
| chr2:232680751 | C | T | 6 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(3): Show |
6 | HG00544.hp2 HG02083.hp2 HG02293.hp2 others(3): Show |
intron_variant | MODIFIER | c.586-834C>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | chr2 | 232680751 | |||||||
| chr2:232680762 | G | C | 2 | a0002c0002t0001g0318 a0002c0002t0001g0327 |
2 | NA19056.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.586-823G>C | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | chr2 | 232680762 | |||||||
| chr2:232680809 | C | T | 25 | a0001c0001t0001g0308 a0001c0001t0006g0025 a0001c0001t0006g0026 others(22): Show |
26 | HG01109.hp2 HG01243.hp1 HG01891.hp1 others(23): Show |
intron_variant | MODIFIER | c.586-776C>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | chr2 | 232680809 | |||||||
| chr2:232680834 | C | A | 138 | a0001c0001t0001g0012 a0002c0002t0001g0001 a0002c0002t0001g0011 others(135): Show |
145 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.586-751C>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | chr2 | 232680834 | |||||||
| chr2:232680849 | C | A | 1 | a0001c0004t0004g0064 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.586-736C>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | chr2 | 232680849 | |||||||
| chr2:232680904 | C | T | 2 | a0002c0003t0001g0166 a0002c0003t0001g0211 |
2 | HG00408.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.586-681C>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | chr2 | 232680904 | |||||||
| chr2:232680907 | C | T | 3 | a0001c0001t0001g0024 a0001c0001t0001g0172 a0001c0001t0001g0356 |
3 | HG03041.hp1 HG03579.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.586-678C>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | chr2 | 232680907 | |||||||
| chr2:232680927 | G | A | 2 | a0004c0007t0001g0006 a0004c0007t0001g0217 |
3 | HG00733.hp2 HG00735.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.586-658G>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | chr2 | 232680927 | |||||||
| chr2:232681014 | GGCAT | G | 14 | a0001c0001t0001g0033 a0001c0001t0001g0036 a0001c0001t0001g0077 others(11): Show |
15 | HG01346.hp1 HG02055.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.586-569_586-566del others(4): Show |
EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr2 | 232681014 | ||||||
| chr2:232681066 | G | A | 1 | a0001c0004t0004g0064 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.586-519G>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | chr2 | 232681066 | |||||||
| chr2:232681180 | A | T | 23 | a0001c0001t0003g0032 a0001c0001t0003g0037 a0001c0001t0003g0266 others(20): Show |
25 | HG01109.hp2 HG02145.hp1 HG02145.hp2 others(22): Show |
intron_variant | MODIFIER | c.586-405A>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | chr2 | 232681180 | |||||||
| chr2:232681208 | A | T | 1 | a0002c0003t0001g0089 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.586-377A>T | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | chr2 | 232681208 | |||||||
| chr2:232681284 | A | G | 1 | a0001c0001t0004g0353 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.586-301A>G | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | chr2 | 232681284 | |||||||
| chr2:232681434 | G | A | 1 | a0002c0003t0001g0086 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.586-151G>A | EFHD1 | ENSG00000115468.13 | transcript | ENST00000264059.8 | protein_coding | 3/3 | chr2 | 232681434 |