Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 30846 |
| ensemblid | ENSG00000024422.12 |
| hgncid | 3243 |
| symbol | EHD2 |
| name | EH domain containing 2 |
| refseq_nuc | NM_014601.4 |
| refseq_prot | NP_055416.2 |
| ensembl_nuc | ENST00000263277.8 |
| ensembl_prot | ENSP00000263277.2 |
| mane_status | MANE Select |
| chr | chr19 |
| start | 47713422 |
| end | 47743134 |
| strand | + |
| ver | v1.2 |
| region | chr19:47713422-47743134 |
| region5000 | chr19:47708422-47748134 |
| regionname0 | EHD2_chr19_47713422_47743134 |
| regionname5000 | EHD2_chr19_47708422_47748134 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 543 | 376 | 90 | 75 | 152 | 18 | 39 | 108 | EHD2_chr19_47708422_47748134 | EHD2 | MFSWL others(538): Show |
chr19 | 47708422 | 47748134 |
| a0002 | 0/0 | 543 | 12 | 8 | 0 | 0 | 0 | 4 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | MFSWL others(538): Show |
chr19 | 47708422 | 47748134 |
| a0003 | 0/0 | 543 | 7 | 0 | 1 | 6 | 0 | 0 | 6 | EHD2_chr19_47708422_47748134 | EHD2 | MFSWL others(538): Show |
chr19 | 47708422 | 47748134 |
| a0004 | 0/0 | 543 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | EHD2_chr19_47708422_47748134 | EHD2 | MFSWL others(538): Show |
chr19 | 47708422 | 47748134 |
| a0005 | 0/0 | 543 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | EHD2_chr19_47708422_47748134 | EHD2 | MFSWL others(538): Show |
chr19 | 47708422 | 47748134 |
| a0006 | 0/0 | 543 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | MFSWL others(538): Show |
chr19 | 47708422 | 47748134 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1629 | 156 | 10 | 36 | 76 | 11 | 23 | EHD2_chr19_47708422_47748134 | EHD2 | ATGTT others(1624): Show |
chr19 | 47708422 | 47748134 | ||
| a0001c0002 | 1/0 | 1629 | 145 | 57 | 23 | 59 | 1 | 4 | EHD2_chr19_47708422_47748134 | EHD2 | ATGTT others(1624): Show |
chr19 | 47708422 | 47748134 | ||
| a0001c0003 | 0/1 | 1629 | 16 | 3 | 4 | 1 | 3 | 4 | EHD2_chr19_47708422_47748134 | EHD2 | ATGTT others(1624): Show |
chr19 | 47708422 | 47748134 | ||
| a0001c0004 | 0/0 | 1629 | 12 | 10 | 0 | 2 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | ATGTT others(1624): Show |
chr19 | 47708422 | 47748134 | ||
| a0001c0005 | 0/0 | 1629 | 8 | 0 | 0 | 8 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | ATGTT others(1624): Show |
chr19 | 47708422 | 47748134 | ||
| a0001c0008 | 0/0 | 1629 | 5 | 0 | 2 | 0 | 2 | 1 | EHD2_chr19_47708422_47748134 | EHD2 | ATGTT others(1624): Show |
chr19 | 47708422 | 47748134 | ||
| a0001c0010 | 0/0 | 1629 | 5 | 1 | 2 | 0 | 0 | 2 | EHD2_chr19_47708422_47748134 | EHD2 | ATGTT others(1624): Show |
chr19 | 47708422 | 47748134 | ||
| a0001c0011 | 0/0 | 1629 | 4 | 0 | 4 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | ATGTT others(1624): Show |
chr19 | 47708422 | 47748134 | ||
| a0001c0012 | 0/0 | 1629 | 4 | 3 | 1 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | ATGTT others(1624): Show |
chr19 | 47708422 | 47748134 | ||
| a0001c0013 | 0/0 | 1629 | 4 | 0 | 2 | 0 | 0 | 2 | EHD2_chr19_47708422_47748134 | EHD2 | ATGTT others(1624): Show |
chr19 | 47708422 | 47748134 | ||
| a0001c0014 | 0/0 | 1629 | 3 | 3 | 0 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | ATGTT others(1624): Show |
chr19 | 47708422 | 47748134 | ||
| a0001c0015 | 0/0 | 1629 | 3 | 0 | 1 | 1 | 0 | 1 | EHD2_chr19_47708422_47748134 | EHD2 | ATGTT others(1624): Show |
chr19 | 47708422 | 47748134 | ||
| a0001c0016 | 0/0 | 1629 | 2 | 0 | 0 | 2 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | ATGTT others(1624): Show |
chr19 | 47708422 | 47748134 | ||
| a0001c0018 | 0/0 | 1629 | 1 | 0 | 0 | 0 | 1 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | ATGTT others(1624): Show |
chr19 | 47708422 | 47748134 | ||
| a0001c0019 | 0/0 | 1629 | 1 | 0 | 0 | 0 | 0 | 1 | EHD2_chr19_47708422_47748134 | EHD2 | ATGTT others(1624): Show |
chr19 | 47708422 | 47748134 | ||
| a0001c0020 | 0/0 | 1629 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | ATGTT others(1624): Show |
chr19 | 47708422 | 47748134 | ||
| a0001c0022 | 0/0 | 1629 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | ATGTT others(1624): Show |
chr19 | 47708422 | 47748134 | ||
| a0001c0023 | 0/0 | 1629 | 1 | 1 | 0 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | ATGTT others(1624): Show |
chr19 | 47708422 | 47748134 | ||
| a0001c0024 | 0/0 | 1629 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | ATGTT others(1624): Show |
chr19 | 47708422 | 47748134 | ||
| a0001c0025 | 0/0 | 1629 | 1 | 1 | 0 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | ATGTT others(1624): Show |
chr19 | 47708422 | 47748134 | ||
| a0001c0026 | 0/0 | 1629 | 1 | 1 | 0 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | ATGTT others(1624): Show |
chr19 | 47708422 | 47748134 | ||
| a0001c0028 | 0/0 | 1629 | 1 | 0 | 0 | 0 | 0 | 1 | EHD2_chr19_47708422_47748134 | EHD2 | ATGTT others(1624): Show |
chr19 | 47708422 | 47748134 | ||
| a0002c0007 | 0/0 | 1629 | 7 | 7 | 0 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | ATGTT others(1624): Show |
chr19 | 47708422 | 47748134 | ||
| a0002c0009 | 0/0 | 1629 | 5 | 1 | 0 | 0 | 0 | 4 | EHD2_chr19_47708422_47748134 | EHD2 | ATGTT others(1624): Show |
chr19 | 47708422 | 47748134 | ||
| a0003c0006 | 0/0 | 1629 | 7 | 0 | 1 | 6 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | ATGTT others(1624): Show |
chr19 | 47708422 | 47748134 | ||
| a0004c0027 | 0/0 | 1629 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | ATGTT others(1624): Show |
chr19 | 47708422 | 47748134 | ||
| a0005c0017 | 0/0 | 1629 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | ATGTT others(1624): Show |
chr19 | 47708422 | 47748134 | ||
| a0006c0021 | 0/0 | 1629 | 1 | 0 | 0 | 0 | 0 | 1 | EHD2_chr19_47708422_47748134 | EHD2 | ATGTT others(1624): Show |
chr19 | 47708422 | 47748134 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3511 | 149 | 6 | 34 | 76 | 11 | 22 | EHD2_chr19_47708422_47748134 | EHD2 | AGACG others(3506): Show |
chr19 | 47708422 | 47748134 |
| a0001c0001t0010 | 0/0 | 3511 | 3 | 3 | 0 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | AGACG others(3506): Show |
chr19 | 47708422 | 47748134 |
| a0001c0001t0013 | 0/0 | 3511 | 1 | 1 | 0 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | AGACG others(3506): Show |
chr19 | 47708422 | 47748134 |
| a0001c0001t0015 | 0/0 | 3511 | 1 | 0 | 1 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | AGACG others(3506): Show |
chr19 | 47708422 | 47748134 |
| a0001c0001t0018 | 0/0 | 3511 | 1 | 0 | 0 | 0 | 0 | 1 | EHD2_chr19_47708422_47748134 | EHD2 | AGACG others(3506): Show |
chr19 | 47708422 | 47748134 |
| a0001c0001t0021 | 0/0 | 3511 | 1 | 0 | 1 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | AGACG others(3506): Show |
chr19 | 47708422 | 47748134 |
| a0001c0002t0002 | 1/0 | 3506 | 92 | 11 | 16 | 59 | 1 | 4 | EHD2_chr19_47708422_47748134 | EHD2 | AGACG others(3501): Show |
chr19 | 47708422 | 47748134 |
| a0001c0002t0003 | 0/0 | 3503 | 27 | 22 | 5 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | AGACG others(3498): Show |
chr19 | 47708422 | 47748134 |
| a0001c0002t0004 | 0/0 | 3512 | 15 | 15 | 0 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | AGACG others(3507): Show |
chr19 | 47708422 | 47748134 |
| a0001c0002t0006 | 0/0 | 3507 | 5 | 4 | 1 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | AGACG others(3502): Show |
chr19 | 47708422 | 47748134 |
| a0001c0002t0008 | 0/0 | 3503 | 2 | 2 | 0 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | AGACG others(3498): Show |
chr19 | 47708422 | 47748134 |
| a0001c0002t0009 | 0/0 | 3506 | 2 | 2 | 0 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | AGACG others(3501): Show |
chr19 | 47708422 | 47748134 |
| a0001c0002t0017 | 0/0 | 3503 | 1 | 1 | 0 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | AGACG others(3498): Show |
chr19 | 47708422 | 47748134 |
| a0001c0002t0020 | 0/0 | 3503 | 1 | 0 | 1 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | AGACG others(3498): Show |
chr19 | 47708422 | 47748134 |
| a0001c0003t0002 | 0/1 | 3506 | 16 | 3 | 4 | 1 | 3 | 4 | EHD2_chr19_47708422_47748134 | EHD2 | AGACG others(3501): Show |
chr19 | 47708422 | 47748134 |
| a0001c0004t0002 | 0/0 | 3506 | 2 | 0 | 0 | 2 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | AGACG others(3501): Show |
chr19 | 47708422 | 47748134 |
| a0001c0004t0003 | 0/0 | 3503 | 3 | 3 | 0 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | AGACG others(3498): Show |
chr19 | 47708422 | 47748134 |
| a0001c0004t0006 | 0/0 | 3507 | 1 | 1 | 0 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | AGACG others(3502): Show |
chr19 | 47708422 | 47748134 |
| a0001c0004t0007 | 0/0 | 3507 | 4 | 4 | 0 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | AGACG others(3502): Show |
chr19 | 47708422 | 47748134 |
| a0001c0004t0009 | 0/0 | 3506 | 1 | 1 | 0 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | AGACG others(3501): Show |
chr19 | 47708422 | 47748134 |
| a0001c0004t0019 | 0/0 | 3507 | 1 | 1 | 0 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | AGACG others(3502): Show |
chr19 | 47708422 | 47748134 |
| a0001c0005t0002 | 0/0 | 3506 | 6 | 0 | 0 | 6 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | AGACG others(3501): Show |
chr19 | 47708422 | 47748134 |
| a0001c0005t0011 | 0/0 | 3506 | 2 | 0 | 0 | 2 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | AGACG others(3501): Show |
chr19 | 47708422 | 47748134 |
| a0001c0008t0005 | 0/0 | 3511 | 5 | 0 | 2 | 0 | 2 | 1 | EHD2_chr19_47708422_47748134 | EHD2 | AGACG others(3506): Show |
chr19 | 47708422 | 47748134 |
| a0001c0010t0005 | 0/0 | 3511 | 4 | 1 | 2 | 0 | 0 | 1 | EHD2_chr19_47708422_47748134 | EHD2 | AGACG others(3506): Show |
chr19 | 47708422 | 47748134 |
| a0001c0010t0016 | 0/0 | 3511 | 1 | 0 | 0 | 0 | 0 | 1 | EHD2_chr19_47708422_47748134 | EHD2 | AGACG others(3506): Show |
chr19 | 47708422 | 47748134 |
| a0001c0011t0001 | 0/0 | 3511 | 3 | 0 | 3 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | AGACG others(3506): Show |
chr19 | 47708422 | 47748134 |
| a0001c0011t0012 | 0/0 | 3511 | 1 | 0 | 1 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | AGACG others(3506): Show |
chr19 | 47708422 | 47748134 |
| a0001c0012t0003 | 0/0 | 3503 | 4 | 3 | 1 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | AGACG others(3498): Show |
chr19 | 47708422 | 47748134 |
| a0001c0013t0001 | 0/0 | 3511 | 4 | 0 | 2 | 0 | 0 | 2 | EHD2_chr19_47708422_47748134 | EHD2 | AGACG others(3506): Show |
chr19 | 47708422 | 47748134 |
| a0001c0014t0008 | 0/0 | 3503 | 3 | 3 | 0 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | AGACG others(3498): Show |
chr19 | 47708422 | 47748134 |
| a0001c0015t0001 | 0/0 | 3511 | 3 | 0 | 1 | 1 | 0 | 1 | EHD2_chr19_47708422_47748134 | EHD2 | AGACG others(3506): Show |
chr19 | 47708422 | 47748134 |
| a0001c0016t0002 | 0/0 | 3506 | 2 | 0 | 0 | 2 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | AGACG others(3501): Show |
chr19 | 47708422 | 47748134 |
| a0001c0018t0005 | 0/0 | 3511 | 1 | 0 | 0 | 0 | 1 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | AGACG others(3506): Show |
chr19 | 47708422 | 47748134 |
| a0001c0019t0001 | 0/0 | 3511 | 1 | 0 | 0 | 0 | 0 | 1 | EHD2_chr19_47708422_47748134 | EHD2 | AGACG others(3506): Show |
chr19 | 47708422 | 47748134 |
| a0001c0020t0001 | 0/0 | 3511 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | AGACG others(3506): Show |
chr19 | 47708422 | 47748134 |
| a0001c0022t0001 | 0/0 | 3511 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | AGACG others(3506): Show |
chr19 | 47708422 | 47748134 |
| a0001c0023t0003 | 0/0 | 3503 | 1 | 1 | 0 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | AGACG others(3498): Show |
chr19 | 47708422 | 47748134 |
| a0001c0024t0001 | 0/0 | 3511 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | AGACG others(3506): Show |
chr19 | 47708422 | 47748134 |
| a0001c0025t0022 | 0/0 | 3506 | 1 | 1 | 0 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | AGACG others(3501): Show |
chr19 | 47708422 | 47748134 |
| a0001c0026t0003 | 0/0 | 3503 | 1 | 1 | 0 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | AGACG others(3498): Show |
chr19 | 47708422 | 47748134 |
| a0001c0028t0001 | 0/0 | 3511 | 1 | 0 | 0 | 0 | 0 | 1 | EHD2_chr19_47708422_47748134 | EHD2 | AGACG others(3506): Show |
chr19 | 47708422 | 47748134 |
| a0002c0007t0003 | 0/0 | 3503 | 1 | 1 | 0 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | AGACG others(3498): Show |
chr19 | 47708422 | 47748134 |
| a0002c0007t0006 | 0/0 | 3507 | 2 | 2 | 0 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | AGACG others(3502): Show |
chr19 | 47708422 | 47748134 |
| a0002c0007t0007 | 0/0 | 3507 | 4 | 4 | 0 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | AGACG others(3502): Show |
chr19 | 47708422 | 47748134 |
| a0002c0009t0001 | 0/0 | 3511 | 5 | 1 | 0 | 0 | 0 | 4 | EHD2_chr19_47708422_47748134 | EHD2 | AGACG others(3506): Show |
chr19 | 47708422 | 47748134 |
| a0003c0006t0001 | 0/0 | 3511 | 7 | 0 | 1 | 6 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | AGACG others(3506): Show |
chr19 | 47708422 | 47748134 |
| a0004c0027t0001 | 0/0 | 3511 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | AGACG others(3506): Show |
chr19 | 47708422 | 47748134 |
| a0005c0017t0014 | 0/0 | 3506 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | AGACG others(3501): Show |
chr19 | 47708422 | 47748134 |
| a0006c0021t0001 | 0/0 | 3511 | 1 | 0 | 0 | 0 | 0 | 1 | EHD2_chr19_47708422_47748134 | EHD2 | AGACG others(3506): Show |
chr19 | 47708422 | 47748134 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0356 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0360 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0369 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0372 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0373 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0374 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0375 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0376 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0377 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0378 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0379 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0380 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0382 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0383 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0384 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0385 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0386 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0387 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0388 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0001g0389 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0010g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0010g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0010g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0013g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0015g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0018g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0001t0021g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0002t0002g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0002t0002g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0002t0002g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0002t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0002t0002g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0002t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0002t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0002t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0002t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0002t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0002t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0002t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0002t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0002t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0002t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0002t0002g0107 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0002t0002g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0002t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0002t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0002t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0002t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0002t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0002t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0002t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0002t0002g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0002t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0002t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0002t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0002t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0002t0002g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0002t0002g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0002t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0002t0002g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0002t0002g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0002t0002g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0002t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0002t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0002t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0002t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0002t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0002t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0002t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0002t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0002t0002g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0002t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0002t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0002t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0002t0002g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0002t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0002t0002g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0002t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0002t0002g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0002t0002g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0002t0002g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0002t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0002t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0002t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0002t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0002t0002g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0002t0002g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0002t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0002t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0002t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0002t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0002t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0002t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0002t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0002t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0002t0002g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0002t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0002t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0002t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0002t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0002t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0002t0002g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0002t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0002t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0002t0002g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0002t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0002t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0002t0002g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0002t0002g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0002t0002g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0002t0002g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0002t0002g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0002t0002g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0002t0002g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0002t0002g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0002t0002g0367 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0002t0002g0390 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0002t0002g0391 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0002t0003g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0002t0003g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0002t0003g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0002t0003g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0002t0003g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0002t0003g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0002t0003g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0002t0003g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0002t0003g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0002t0003g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0002t0003g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0002t0003g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0002t0003g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0002t0003g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0002t0003g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0002t0003g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0002t0003g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0002t0003g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0002t0003g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0002t0003g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0002t0003g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0002t0003g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0002t0003g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0002t0003g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0002t0003g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0002t0003g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0002t0004g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0002t0004g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0002t0004g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0002t0004g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0002t0004g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0002t0004g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0002t0004g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0002t0004g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0002t0004g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0002t0004g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0002t0004g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0002t0004g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0002t0004g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0002t0004g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0002t0004g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0002t0006g0003 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0002t0006g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0002t0006g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0002t0006g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0002t0008g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0002t0008g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0002t0009g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0002t0009g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0002t0017g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0002t0020g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0003t0002g0005 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0003t0002g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0003t0002g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0003t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0003t0002g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0003t0002g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0003t0002g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0003t0002g0321 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0003t0002g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0003t0002g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0003t0002g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0003t0002g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0003t0002g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0003t0002g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0003t0002g0366 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0004t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0004t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0004t0003g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0004t0003g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0004t0003g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0004t0006g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0004t0007g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0004t0007g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0004t0007g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0004t0007g0392 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0004t0009g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0004t0019g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0005t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0005t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0005t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0005t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0005t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0005t0002g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0005t0011g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0005t0011g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0008t0005g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0008t0005g0363 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0008t0005g0364 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0008t0005g0365 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0008t0005g0381 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0010t0005g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0010t0005g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0010t0005g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0010t0005g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0010t0016g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0011t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0011t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0011t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0011t0012g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0012t0003g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0012t0003g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0012t0003g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0013t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0013t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0013t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0013t0001g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0014t0008g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0014t0008g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0015t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0015t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0015t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0016t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0016t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0018t0005g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0019t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0020t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0022t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0023t0003g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0024t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0025t0022g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0026t0003g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0001c0028t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0002c0007t0003g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0002c0007t0006g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0002c0007t0006g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0002c0007t0007g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0002c0007t0007g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0002c0007t0007g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0002c0007t0007g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0002c0009t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0002c0009t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0002c0009t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0002c0009t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0002c0009t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0003c0006t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0003c0006t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0003c0006t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0003c0006t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0003c0006t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0003c0006t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0003c0006t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0004c0027t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0005c0017t0014g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| a0006c0021t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0003 | t0002 | g0366 | EUR | GBR | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG00099 | hp2 | a0001 | c0008 | t0005 | g0363 | EUR | GBR | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0083 | EUR | GBR | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0123 | EUR | GBR | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG00280 | hp1 | a0001 | c0018 | t0005 | g0086 | EUR | FIN | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0019 | EUR | FIN | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0375 | EUR | FIN | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0153 | EUR | FIN | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | CHS | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0376 | EAS | CHS | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0357 | EAS | CHS | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | CHS | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0358 | EAS | CHS | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | CHS | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | CHS | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0382 | EAS | CHS | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | CHS | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG00558 | hp2 | a0001 | c0002 | t0002 | g0244 | EAS | CHS | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | CHS | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | CHS | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0311 | AMR | PUR | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0226 | AMR | PUR | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG00642 | hp1 | a0001 | c0003 | t0002 | g0039 | AMR | PUR | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG00642 | hp2 | a0003 | c0006 | t0001 | g0071 | AMR | PUR | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | CHS | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | CHS | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0313 | AMR | PUR | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG00738 | hp1 | a0001 | c0012 | t0003 | g0346 | AMR | PUR | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | PUR | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG00741 | hp1 | a0001 | c0008 | t0005 | g0364 | AMR | PUR | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG01069 | hp1 | a0001 | c0002 | t0003 | g0178 | AMR | PUR | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0387 | AMR | PUR | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG01070 | hp1 | a0001 | c0011 | t0001 | g0210 | AMR | PUR | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG01070 | hp2 | a0001 | c0003 | t0002 | g0316 | AMR | PUR | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0385 | AMR | PUR | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG01071 | hp2 | a0001 | c0011 | t0001 | g0209 | AMR | PUR | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG01074 | hp2 | a0001 | c0015 | t0001 | g0302 | AMR | PUR | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0373 | AMR | PUR | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0222 | AMR | PUR | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG01106 | hp2 | a0001 | c0002 | t0002 | g0367 | AMR | PUR | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0334 | AMR | PUR | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG01167 | hp1 | a0001 | c0002 | t0002 | g0184 | AMR | PUR | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0208 | AMR | PUR | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0279 | AMR | PUR | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0314 | AMR | PUR | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0328 | AMR | PUR | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG01169 | hp2 | a0001 | c0002 | t0002 | g0185 | AMR | PUR | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0141 | AMR | PUR | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG01175 | hp2 | a0001 | c0002 | t0002 | g0323 | AMR | PUR | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG01192 | hp1 | a0001 | c0011 | t0001 | g0142 | AMR | PUR | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0359 | AMR | PUR | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG01243 | hp1 | a0001 | c0010 | t0005 | g0017 | AMR | PUR | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG01243 | hp2 | a0001 | c0002 | t0006 | g0003 | AMR | PUR | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG01255 | hp1 | a0001 | c0010 | t0005 | g0012 | AMR | CLM | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | CLM | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG01256 | hp1 | a0001 | c0002 | t0002 | g0264 | AMR | CLM | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG01256 | hp2 | a0001 | c0013 | t0001 | g0014 | AMR | CLM | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG01258 | hp1 | a0001 | c0001 | t0015 | g0091 | AMR | CLM | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG01258 | hp2 | a0001 | c0013 | t0001 | g0013 | AMR | CLM | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG01261 | hp1 | a0001 | c0002 | t0002 | g0182 | AMR | CLM | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG01261 | hp2 | a0001 | c0002 | t0002 | g0036 | AMR | CLM | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG01346 | hp1 | a0001 | c0002 | t0002 | g0231 | AMR | CLM | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG01346 | hp2 | a0001 | c0008 | t0005 | g0341 | AMR | CLM | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | CLM | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG01358 | hp2 | a0001 | c0011 | t0012 | g0077 | AMR | CLM | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG01361 | hp1 | a0001 | c0002 | t0002 | g0243 | AMR | CLM | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG01361 | hp2 | a0001 | c0003 | t0002 | g0327 | AMR | CLM | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG01433 | hp1 | a0001 | c0003 | t0002 | g0008 | AMR | CLM | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG01433 | hp2 | a0001 | c0002 | t0002 | g0252 | AMR | CLM | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0384 | AMR | CLM | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | CLM | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0325 | EUR | IBS | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0388 | EUR | IBS | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG01516 | hp1 | a0001 | c0003 | t0002 | g0005 | EUR | IBS | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0028 | EUR | IBS | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG01517 | hp1 | a0001 | c0003 | t0002 | g0005 | EUR | IBS | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0386 | EUR | IBS | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG01884 | hp1 | a0001 | c0002 | t0004 | g0331 | AFR | ACB | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG01884 | hp2 | a0001 | c0002 | t0004 | g0299 | AFR | ACB | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG01891 | hp1 | a0001 | c0002 | t0004 | g0148 | AFR | ACB | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG01891 | hp2 | a0001 | c0004 | t0003 | g0183 | AFR | ACB | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG01928 | hp1 | a0001 | c0002 | t0002 | g0163 | AMR | PEL | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG01928 | hp2 | a0001 | c0002 | t0020 | g0180 | AMR | PEL | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0336 | AMR | PEL | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0095 | AMR | PEL | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0356 | AMR | PEL | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | PEL | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG01952 | hp1 | a0001 | c0002 | t0002 | g0223 | AMR | PEL | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG01952 | hp2 | a0001 | c0002 | t0002 | g0241 | AMR | PEL | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG01975 | hp1 | a0001 | c0002 | t0002 | g0170 | AMR | PEL | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0242 | AMR | PEL | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG01993 | hp1 | a0001 | c0002 | t0003 | g0176 | AMR | PEL | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0189 | AMR | PEL | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG02015 | hp1 | a0001 | c0002 | t0002 | g0198 | EAS | KHV | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | KHV | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG02027 | hp1 | a0001 | c0002 | t0002 | g0188 | EAS | KHV | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG02027 | hp2 | a0001 | c0002 | t0002 | g0140 | EAS | KHV | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | KHV | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG02040 | hp2 | a0001 | c0004 | t0002 | g0043 | EAS | KHV | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG02055 | hp1 | a0001 | c0002 | t0004 | g0147 | AFR | ACB | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG02055 | hp2 | a0001 | c0002 | t0003 | g0031 | AFR | ACB | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG02056 | hp1 | a0001 | c0002 | t0002 | g0233 | EAS | KHV | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG02056 | hp2 | a0001 | c0004 | t0002 | g0237 | EAS | KHV | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | KHV | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG02071 | hp2 | a0001 | c0002 | t0002 | g0168 | EAS | KHV | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | KHV | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG02074 | hp2 | a0001 | c0016 | t0002 | g0067 | EAS | KHV | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG02083 | hp1 | a0001 | c0002 | t0002 | g0254 | EAS | KHV | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0377 | EAS | KHV | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG02129 | hp1 | a0001 | c0016 | t0002 | g0060 | EAS | KHV | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0368 | EAS | KHV | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | KHV | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG02132 | hp2 | a0001 | c0002 | t0002 | g0278 | EAS | KHV | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | KHV | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG02135 | hp2 | a0001 | c0002 | t0002 | g0273 | EAS | KHV | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG02145 | hp1 | a0001 | c0023 | t0003 | g0343 | AFR | ACB | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG02145 | hp2 | a0002 | c0007 | t0007 | g0290 | AFR | ACB | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | PEL | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG02148 | hp2 | a0001 | c0001 | t0021 | g0079 | AMR | PEL | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | CDX | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | CDX | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG02165 | hp1 | a0001 | c0002 | t0002 | g0174 | EAS | CDX | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG02165 | hp2 | a0001 | c0002 | t0002 | g0049 | EAS | CDX | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG02257 | hp1 | a0001 | c0002 | t0002 | g0312 | AFR | ACB | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG02257 | hp2 | a0002 | c0007 | t0006 | g0037 | AFR | ACB | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG02258 | hp1 | a0001 | c0002 | t0004 | g0149 | AFR | ACB | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0303 | AFR | ACB | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG02273 | hp1 | a0001 | c0002 | t0003 | g0181 | AMR | PEL | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG02273 | hp2 | a0001 | c0002 | t0003 | g0179 | AMR | PEL | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG02280 | hp1 | a0001 | c0002 | t0006 | g0026 | AFR | ACB | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG02280 | hp2 | a0001 | c0002 | t0003 | g0294 | AFR | ACB | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG02293 | hp1 | a0001 | c0002 | t0002 | g0335 | AMR | PEL | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG02293 | hp2 | a0001 | c0002 | t0003 | g0175 | AMR | PEL | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG02300 | hp1 | a0001 | c0002 | t0002 | g0275 | AMR | PEL | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | PEL | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG02451 | hp1 | a0001 | c0002 | t0002 | g0204 | AFR | ACB | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG02451 | hp2 | a0001 | c0002 | t0003 | g0287 | AFR | ACB | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0383 | EAS | KHV | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG02523 | hp2 | a0001 | c0002 | t0002 | g0322 | EAS | KHV | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG02572 | hp1 | a0001 | c0003 | t0002 | g0362 | AFR | GWD | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG02572 | hp2 | a0001 | c0002 | t0002 | g0171 | AFR | GWD | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0372 | SAS | PJL | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0062 | SAS | PJL | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG02615 | hp1 | a0001 | c0002 | t0003 | g0292 | AFR | GWD | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG02615 | hp2 | a0001 | c0002 | t0002 | g0333 | AFR | GWD | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG02622 | hp1 | a0002 | c0007 | t0003 | g0032 | AFR | GWD | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG02622 | hp2 | a0001 | c0002 | t0003 | g0352 | AFR | GWD | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0347 | AFR | GWD | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG02630 | hp2 | a0001 | c0004 | t0007 | g0065 | AFR | GWD | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG02647 | hp1 | a0001 | c0002 | t0004 | g0038 | AFR | GWD | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG02647 | hp2 | a0001 | c0002 | t0002 | g0042 | AFR | GWD | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG02683 | hp1 | a0001 | c0003 | t0002 | g0324 | SAS | PJL | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG02683 | hp2 | a0001 | c0010 | t0005 | g0284 | SAS | PJL | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0128 | SAS | PJL | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG02698 | hp2 | a0002 | c0009 | t0001 | g0280 | SAS | PJL | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG02717 | hp1 | a0001 | c0002 | t0003 | g0225 | AFR | GWD | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG02717 | hp2 | a0001 | c0002 | t0002 | g0318 | AFR | GWD | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG02723 | hp1 | a0001 | c0001 | t0013 | g0072 | AFR | GWD | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG02723 | hp2 | a0001 | c0002 | t0003 | g0301 | AFR | GWD | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0274 | SAS | PJL | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0154 | SAS | PJL | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0215 | SAS | PJL | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG02738 | hp2 | a0001 | c0003 | t0002 | g0340 | SAS | PJL | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG02809 | hp1 | a0001 | c0002 | t0003 | g0004 | AFR | GWD | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG02809 | hp2 | a0001 | c0002 | t0003 | g0027 | AFR | GWD | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG02818 | hp2 | a0001 | c0002 | t0006 | g0033 | AFR | GWD | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG02886 | hp1 | a0002 | c0007 | t0006 | g0034 | AFR | GWD | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG02886 | hp2 | a0001 | c0002 | t0002 | g0319 | AFR | GWD | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG02895 | hp1 | a0001 | c0002 | t0002 | g0009 | AFR | GWD | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG02895 | hp2 | a0001 | c0002 | t0002 | g0040 | AFR | GWD | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG02896 | hp1 | a0001 | c0012 | t0003 | g0006 | AFR | GWD | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG02896 | hp2 | a0001 | c0002 | t0004 | g0064 | AFR | GWD | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG02897 | hp1 | a0001 | c0002 | t0002 | g0007 | AFR | GWD | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG02897 | hp2 | a0001 | c0012 | t0003 | g0006 | AFR | GWD | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG02922 | hp1 | a0001 | c0004 | t0006 | g0272 | AFR | ESN | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG02922 | hp2 | a0001 | c0002 | t0003 | g0282 | AFR | ESN | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG02965 | hp1 | a0001 | c0002 | t0003 | g0306 | AFR | ESN | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG02965 | hp2 | a0001 | c0014 | t0008 | g0002 | AFR | ESN | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG02970 | hp1 | a0001 | c0004 | t0009 | g0029 | AFR | ESN | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG02970 | hp2 | a0001 | c0012 | t0003 | g0349 | AFR | ESN | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG02976 | hp1 | a0001 | c0002 | t0003 | g0289 | AFR | ESN | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG02976 | hp2 | a0002 | c0009 | t0001 | g0035 | AFR | ESN | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0117 | SAS | PJL | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG03017 | hp2 | a0002 | c0009 | t0001 | g0131 | SAS | PJL | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0337 | AFR | GWD | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG03041 | hp2 | a0002 | c0007 | t0007 | g0291 | AFR | GWD | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG03098 | hp1 | a0001 | c0014 | t0008 | g0293 | AFR | MSL | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG03098 | hp2 | a0001 | c0004 | t0003 | g0021 | AFR | MSL | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG03139 | hp1 | a0001 | c0002 | t0003 | g0307 | AFR | ESN | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG03139 | hp2 | a0001 | c0004 | t0003 | g0022 | AFR | ESN | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG03195 | hp1 | a0001 | c0002 | t0008 | g0286 | AFR | ESN | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG03195 | hp2 | a0001 | c0001 | t0010 | g0300 | AFR | ESN | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG03209 | hp1 | a0001 | c0002 | t0009 | g0150 | AFR | MSL | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG03209 | hp2 | a0001 | c0001 | t0010 | g0350 | AFR | MSL | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG03225 | hp1 | a0001 | c0002 | t0004 | g0297 | AFR | MSL | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG03225 | hp2 | a0001 | c0002 | t0004 | g0059 | AFR | MSL | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG03239 | hp1 | a0002 | c0009 | t0001 | g0130 | SAS | PJL | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0270 | SAS | PJL | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG03453 | hp1 | a0001 | c0004 | t0007 | g0361 | AFR | MSL | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG03453 | hp2 | a0001 | c0026 | t0003 | g0295 | AFR | MSL | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG03486 | hp1 | a0001 | c0014 | t0008 | g0002 | AFR | MSL | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG03486 | hp2 | a0001 | c0002 | t0004 | g0281 | AFR | MSL | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0076 | SAS | PJL | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0309 | SAS | PJL | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0096 | SAS | PJL | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0136 | SAS | PJL | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG03516 | hp1 | a0001 | c0002 | t0003 | g0020 | AFR | ESN | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG03516 | hp2 | a0002 | c0007 | t0007 | g0296 | AFR | ESN | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG03540 | hp1 | a0001 | c0002 | t0003 | g0348 | AFR | GWD | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG03540 | hp2 | a0001 | c0002 | t0004 | g0330 | AFR | GWD | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG03579 | hp1 | a0001 | c0002 | t0006 | g0304 | AFR | MSL | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG03579 | hp2 | a0001 | c0002 | t0004 | g0146 | AFR | MSL | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG03669 | hp1 | a0001 | c0002 | t0002 | g0228 | SAS | PJL | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG03669 | hp2 | a0001 | c0010 | t0016 | g0011 | SAS | PJL | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0268 | SAS | STU | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG03688 | hp2 | a0001 | c0019 | t0001 | g0134 | SAS | STU | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG03704 | hp1 | a0001 | c0013 | t0001 | g0016 | SAS | PJL | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0369 | SAS | PJL | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0235 | SAS | PJL | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG03710 | hp2 | a0001 | c0003 | t0002 | g0326 | SAS | PJL | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG03831 | hp1 | a0001 | c0008 | t0005 | g0381 | SAS | BEB | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0271 | SAS | BEB | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0088 | SAS | BEB | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0224 | SAS | BEB | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG03927 | hp1 | a0001 | c0003 | t0002 | g0310 | SAS | BEB | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG03927 | hp2 | a0001 | c0028 | t0001 | g0283 | SAS | BEB | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0360 | SAS | BEB | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG03942 | hp2 | a0001 | c0013 | t0001 | g0018 | SAS | BEB | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG04115 | hp1 | a0001 | c0001 | t0018 | g0044 | SAS | STU | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0211 | SAS | STU | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG04184 | hp1 | a0001 | c0002 | t0002 | g0230 | SAS | BEB | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG04184 | hp2 | a0001 | c0002 | t0002 | g0220 | SAS | BEB | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG04199 | hp1 | a0001 | c0002 | t0002 | g0305 | SAS | STU | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0078 | SAS | STU | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG04204 | hp1 | a0001 | c0015 | t0001 | g0104 | SAS | STU | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0101 | SAS | STU | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| NA18522 | hp1 | a0001 | c0002 | t0003 | g0004 | AFR | YRI | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| NA18522 | hp2 | a0001 | c0002 | t0009 | g0338 | AFR | YRI | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| NA18612 | hp1 | a0001 | c0015 | t0001 | g0236 | EAS | CHB | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| NA18612 | hp2 | a0001 | c0005 | t0002 | g0157 | EAS | CHB | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| NA18747 | hp1 | a0001 | c0002 | t0002 | g0138 | EAS | CHB | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | CHB | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| NA18906 | hp1 | a0002 | c0007 | t0007 | g0342 | AFR | YRI | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| NA18906 | hp2 | a0001 | c0002 | t0003 | g0320 | AFR | YRI | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| NA18940 | hp1 | a0001 | c0002 | t0002 | g0253 | EAS | JPT | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| NA18940 | hp2 | a0001 | c0002 | t0002 | g0025 | EAS | JPT | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| NA18943 | hp1 | a0001 | c0002 | t0002 | g0251 | EAS | JPT | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| NA18944 | hp2 | a0001 | c0002 | t0002 | g0047 | EAS | JPT | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| NA18947 | hp1 | a0001 | c0005 | t0011 | g0159 | EAS | JPT | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| NA18947 | hp2 | a0001 | c0002 | t0002 | g0194 | EAS | JPT | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| NA18948 | hp2 | a0001 | c0022 | t0001 | g0099 | EAS | JPT | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| NA18949 | hp1 | a0001 | c0002 | t0002 | g0245 | EAS | JPT | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0380 | EAS | JPT | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| NA18956 | hp2 | a0001 | c0002 | t0002 | g0247 | EAS | JPT | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| NA18957 | hp1 | a0001 | c0002 | t0002 | g0186 | EAS | JPT | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| NA18957 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| NA18959 | hp2 | a0001 | c0002 | t0002 | g0166 | EAS | JPT | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| NA18960 | hp1 | a0001 | c0002 | t0002 | g0143 | EAS | JPT | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| NA18961 | hp1 | a0001 | c0020 | t0001 | g0045 | EAS | JPT | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| NA18961 | hp2 | a0001 | c0005 | t0002 | g0156 | EAS | JPT | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| NA18963 | hp1 | a0001 | c0002 | t0002 | g0248 | EAS | JPT | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| NA18963 | hp2 | a0001 | c0002 | t0002 | g0221 | EAS | JPT | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| NA18966 | hp1 | a0001 | c0002 | t0002 | g0167 | EAS | JPT | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0355 | EAS | JPT | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| NA18968 | hp2 | a0001 | c0002 | t0002 | g0069 | EAS | JPT | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| NA18970 | hp2 | a0001 | c0002 | t0002 | g0162 | EAS | JPT | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| NA18971 | hp2 | a0003 | c0006 | t0001 | g0161 | EAS | JPT | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| NA18975 | hp1 | a0001 | c0005 | t0002 | g0187 | EAS | JPT | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| NA18978 | hp1 | a0001 | c0002 | t0002 | g0250 | EAS | JPT | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| NA18978 | hp2 | a0003 | c0006 | t0001 | g0155 | EAS | JPT | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| NA18980 | hp2 | a0001 | c0002 | t0002 | g0201 | EAS | JPT | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| NA18982 | hp1 | a0001 | c0002 | t0002 | g0051 | EAS | JPT | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| NA18983 | hp1 | a0004 | c0027 | t0001 | g0108 | EAS | JPT | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| NA18984 | hp1 | a0001 | c0002 | t0002 | g0227 | EAS | JPT | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0389 | EAS | JPT | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| NA18985 | hp1 | a0001 | c0002 | t0002 | g0193 | EAS | JPT | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| NA18988 | hp1 | a0001 | c0002 | t0002 | g0269 | EAS | JPT | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| NA18989 | hp1 | a0001 | c0002 | t0002 | g0276 | EAS | JPT | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| NA18998 | hp1 | a0001 | c0002 | t0002 | g0217 | EAS | JPT | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| NA18998 | hp2 | a0001 | c0003 | t0002 | g0139 | EAS | JPT | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| NA18999 | hp1 | a0001 | c0002 | t0002 | g0246 | EAS | JPT | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| NA19000 | hp1 | a0001 | c0024 | t0001 | g0329 | EAS | JPT | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| NA19001 | hp2 | a0001 | c0005 | t0011 | g0158 | EAS | JPT | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| NA19004 | hp1 | a0001 | c0005 | t0002 | g0265 | EAS | JPT | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| NA19004 | hp2 | a0001 | c0002 | t0002 | g0124 | EAS | JPT | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| NA19009 | hp2 | a0001 | c0002 | t0002 | g0164 | EAS | JPT | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| NA19011 | hp1 | a0001 | c0002 | t0002 | g0263 | EAS | JPT | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| NA19011 | hp2 | a0001 | c0002 | t0002 | g0234 | EAS | JPT | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| NA19030 | hp1 | a0001 | c0002 | t0004 | g0172 | AFR | LWK | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| NA19030 | hp2 | a0001 | c0002 | t0004 | g0332 | AFR | LWK | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| NA19043 | hp1 | a0001 | c0003 | t0002 | g0339 | AFR | LWK | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| NA19043 | hp2 | a0001 | c0002 | t0003 | g0030 | AFR | LWK | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| NA19054 | hp2 | a0001 | c0002 | t0002 | g0240 | EAS | JPT | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0379 | EAS | JPT | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| NA19058 | hp1 | a0001 | c0002 | t0002 | g0054 | EAS | JPT | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| NA19063 | hp2 | a0001 | c0002 | t0002 | g0239 | EAS | JPT | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| NA19064 | hp2 | a0001 | c0002 | t0002 | g0390 | EAS | JPT | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| NA19066 | hp1 | a0003 | c0006 | t0001 | g0214 | EAS | JPT | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0371 | EAS | JPT | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| NA19067 | hp1 | a0001 | c0002 | t0002 | g0216 | EAS | JPT | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| NA19067 | hp2 | a0001 | c0002 | t0002 | g0258 | EAS | JPT | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| NA19074 | hp2 | a0001 | c0002 | t0002 | g0249 | EAS | JPT | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0354 | EAS | JPT | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| NA19076 | hp2 | a0005 | c0017 | t0014 | g0206 | EAS | JPT | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| NA19079 | hp1 | a0001 | c0002 | t0002 | g0127 | EAS | JPT | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| NA19079 | hp2 | a0001 | c0005 | t0002 | g0370 | EAS | JPT | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| NA19080 | hp2 | a0001 | c0002 | t0002 | g0052 | EAS | JPT | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| NA19081 | hp1 | a0001 | c0005 | t0002 | g0105 | EAS | JPT | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| NA19082 | hp1 | a0001 | c0002 | t0002 | g0391 | EAS | JPT | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| NA19083 | hp2 | a0001 | c0002 | t0002 | g0195 | EAS | JPT | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| NA19084 | hp1 | a0003 | c0006 | t0001 | g0160 | EAS | JPT | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| NA19084 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| NA19085 | hp2 | a0001 | c0002 | t0002 | g0053 | EAS | JPT | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| NA19086 | hp1 | a0001 | c0002 | t0002 | g0205 | EAS | JPT | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| NA19086 | hp2 | a0003 | c0006 | t0001 | g0213 | EAS | JPT | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| NA19087 | hp1 | a0001 | c0002 | t0002 | g0200 | EAS | JPT | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| NA19087 | hp2 | a0003 | c0006 | t0001 | g0212 | EAS | JPT | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| NA19088 | hp1 | a0001 | c0002 | t0002 | g0257 | EAS | JPT | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| NA19240 | hp1 | a0001 | c0002 | t0003 | g0353 | AFR | YRI | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| NA19240 | hp2 | a0001 | c0002 | t0006 | g0003 | AFR | YRI | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| NA20129 | hp1 | a0001 | c0002 | t0017 | g0298 | AFR | ASW | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| NA20129 | hp2 | a0001 | c0004 | t0007 | g0392 | AFR | ASW | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| NA20752 | hp1 | a0001 | c0008 | t0005 | g0365 | EUR | TSI | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0197 | EUR | TSI | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0317 | EUR | TSI | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| NA20805 | hp2 | a0001 | c0002 | t0002 | g0120 | EUR | TSI | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| NA20905 | hp1 | a0002 | c0009 | t0001 | g0132 | SAS | GIH | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| NA20905 | hp2 | a0006 | c0021 | t0001 | g0085 | SAS | GIH | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG02109 | hp1 | a0001 | c0002 | t0002 | g0041 | AFR | ACB | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG02109 | hp2 | a0001 | c0004 | t0019 | g0023 | AFR | ACB | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG02486 | hp1 | a0001 | c0002 | t0008 | g0285 | AFR | ACB | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG02486 | hp2 | a0001 | c0002 | t0003 | g0070 | AFR | ACB | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0378 | AFR | ACB | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG02559 | hp2 | a0001 | c0025 | t0022 | g0345 | AFR | ACB | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG03471 | hp1 | a0001 | c0001 | t0010 | g0344 | AFR | MSL | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG03471 | hp2 | a0001 | c0002 | t0003 | g0288 | AFR | MSL | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG06807 | hp1 | a0001 | c0004 | t0007 | g0063 | AFR | USA | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | USA | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| NA18955 | hp1 | a0001 | c0002 | t0002 | g0137 | EAS | JPT | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0374 | EAS | JPT | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| NA20300 | hp1 | a0001 | c0002 | t0004 | g0351 | AFR | USA | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| NA20300 | hp2 | a0001 | c0003 | t0002 | g0315 | AFR | USA | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| NA21309 | hp1 | a0001 | c0002 | t0003 | g0308 | AFR | LWK | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| NA21309 | hp2 | a0001 | c0010 | t0005 | g0015 | AFR | LWK | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| homoSapiens | chm13v2 | a0001 | c0003 | t0002 | g0321 | REF | REF | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0002 | g0107 | REF | REF | EHD2_chr19_47708422_47748134 | EHD2 | chr19 | 47708422 | 47748134 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:47716755 | C | T | 1 | a0002 | 12 | HG02145.hp2 HG02257.hp2 HG02622.hp1 others(9): Show |
missense_variant | MODERATE | c.143C>T | p.Pro48Leu | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 2/6 | 315/3506 | 143/1632 | 48/543 | chr19 | 47716755 | |||
| chr19:47716925 | A | G | 1 | a0004 | 1 | NA18983.hp1 | missense_variant | MODERATE | c.313A>G | p.Thr105Ala | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 2/6 | 485/3506 | 313/1632 | 105/543 | chr19 | 47716925 | |||
| chr19:47726147 | C | T | 1 | a0003 | 7 | HG00642.hp2 NA18971.hp2 NA18978.hp2 others(4): Show |
missense_variant | MODERATE | c.838C>T | p.Arg280Cys | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/6 | 1010/3506 | 838/1632 | 280/543 | chr19 | 47726147 | |||
| chr19:47736495 | A | G | 1 | a0006 | 1 | NA20905.hp2 | missense_variant | MODERATE | c.1042A>G | p.Ile348Val | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 5/6 | 1214/3506 | 1042/1632 | 348/543 | chr19 | 47736495 | |||
| chr19:47736516 | G | C | 1 | a0005 | 1 | NA19076.hp2 | missense_variant | MODERATE | c.1063G>C | p.Asp355His | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 5/6 | 1235/3506 | 1063/1632 | 355/543 | chr19 | 47736516 | |||
| chr19:47736517 | A | G | 1 | a0005 | 1 | NA19076.hp2 | missense_variant | MODERATE | c.1064A>G | p.Asp355Gly | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 5/6 | 1236/3506 | 1064/1632 | 355/543 | chr19 | 47736517 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:47716636 | C | T | 3 | a0001c0010 a0001c0013 a0001c0028 |
10 | HG01243.hp1 HG01255.hp1 HG01256.hp2 others(7): Show |
synonymous_variant | LOW | c.24C>T | p.Gly8Gly | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 2/6 | 196/3506 | 24/1632 | 8/543 | chr19 | 47716636 | |||
| chr19:47716672 | G | A | 1 | a0001c0011 | 4 | HG01070.hp1 HG01071.hp2 HG01192.hp1 others(1): Show |
synonymous_variant | LOW | c.60G>A | p.Thr20Thr | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 2/6 | 232/3506 | 60/1632 | 20/543 | chr19 | 47716672 | |||
| chr19:47716996 | C | T | 3 | a0001c0012 a0001c0025 a0001c0026 |
6 | HG00738.hp1 HG02559.hp2 HG02896.hp1 others(3): Show |
synonymous_variant | LOW | c.384C>T | p.Phe128Phe | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 2/6 | 556/3506 | 384/1632 | 128/543 | chr19 | 47716996 | |||
| chr19:47725912 | A | G | 8 | a0001c0004 a0001c0008 a0001c0010 others(5): Show |
29 | HG00099.hp2 HG00741.hp1 HG01074.hp2 others(26): Show |
synonymous_variant | LOW | c.603A>G | p.Ser201Ser | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/6 | 775/3506 | 603/1632 | 201/543 | chr19 | 47725912 | |||
| chr19:47736389 | C | T | 1 | a0001c0024 | 1 | NA19000.hp1 | synonymous_variant | LOW | c.936C>T | p.Ser312Ser | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 5/6 | 1108/3506 | 936/1632 | 312/543 | chr19 | 47736389 | |||
| chr19:47736461 | C | T | 1 | a0001c0022 | 1 | NA18948.hp2 | synonymous_variant | LOW | c.1008C>T | p.Pro336Pro | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 5/6 | 1180/3506 | 1008/1632 | 336/543 | chr19 | 47736461 | |||
| chr19:47740907 | C | T | 1 | a0001c0016 | 2 | HG02074.hp2 HG02129.hp1 |
synonymous_variant | LOW | c.1107C>T | p.Thr369Thr | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 6/6 | 1279/3506 | 1107/1632 | 369/543 | chr19 | 47740907 | |||
| chr19:47740937 | A | G | 16 | a0001c0001 a0001c0008 a0001c0010 others(13): Show |
197 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(194): Show |
synonymous_variant | LOW | c.1137A>G | p.Leu379Leu | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 6/6 | 1309/3506 | 1137/1632 | 379/543 | chr19 | 47740937 | |||
| chr19:47740964 | C | T | 1 | a0001c0023 | 1 | HG02145.hp1 | synonymous_variant | LOW | c.1164C>T | p.His388His | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 6/6 | 1336/3506 | 1164/1632 | 388/543 | chr19 | 47740964 | |||
| chr19:47741120 | C | T | 1 | a0001c0005 | 8 | NA18612.hp2 NA18947.hp1 NA18961.hp2 others(5): Show |
synonymous_variant | LOW | c.1320C>T | p.Asp440Asp | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 6/6 | 1492/3506 | 1320/1632 | 440/543 | chr19 | 47741120 | |||
| chr19:47741144 | G | A | 2 | a0001c0003 a0001c0025 |
16 | HG00099.hp1 HG00642.hp1 HG01070.hp2 others(13): Show |
synonymous_variant | LOW | c.1344G>A | p.Lys448Lys | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 6/6 | 1516/3506 | 1344/1632 | 448/543 | chr19 | 47741144 | |||
| chr19:47741162 | C | T | 1 | a0001c0020 | 1 | NA18961.hp1 | synonymous_variant | LOW | c.1362C>T | p.Asp454Asp | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 6/6 | 1534/3506 | 1362/1632 | 454/543 | chr19 | 47741162 | |||
| chr19:47741204 | C | T | 1 | a0001c0019 | 1 | HG03688.hp2 | synonymous_variant | LOW | c.1404C>T | p.Ser468Ser | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 6/6 | 1576/3506 | 1404/1632 | 468/543 | chr19 | 47741204 | |||
| chr19:47741312 | G | A | 13 | a0001c0001 a0001c0011 a0001c0013 others(10): Show |
186 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(183): Show |
synonymous_variant | LOW | c.1512G>A | p.Glu504Glu | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 6/6 | 1684/3506 | 1512/1632 | 504/543 | chr19 | 47741312 | |||
| chr19:47741342 | G | A | 1 | a0001c0014 | 3 | HG02965.hp2 HG03098.hp1 HG03486.hp1 |
synonymous_variant | LOW | c.1542G>A | p.Glu514Glu | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 6/6 | 1714/3506 | 1542/1632 | 514/543 | chr19 | 47741342 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:47713430 | C | G | 1 | a0001c0025t0022 | 1 | HG02559.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-164C>G | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 1/6 | chr19 | 47713430 | |||||||
| chr19:47713459 | C | G | 1 | a0001c0005t0011 | 2 | NA18947.hp1 NA19001.hp2 |
5_prime_UTR_variant | MODIFIER | c.-135C>G | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 1/6 | 3154 | chr19 | 47713459 | ||||||
| chr19:47713490 | C | A | 1 | a0001c0011t0012 | 1 | HG01358.hp2 | 5_prime_UTR_variant | MODIFIER | c.-104C>A | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 1/6 | 3123 | chr19 | 47713490 | ||||||
| chr19:47713492 | C | T | 1 | a0001c0001t0021 | 1 | HG02148.hp2 | 5_prime_UTR_variant | MODIFIER | c.-102C>T | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 1/6 | 3121 | chr19 | 47713492 | ||||||
| chr19:47713531 | C | A | 1 | a0001c0001t0013 | 1 | HG02723.hp1 | 5_prime_UTR_variant | MODIFIER | c.-63C>A | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 1/6 | 3082 | chr19 | 47713531 | ||||||
| chr19:47741435 | C | CG | 40 | a0001c0001t0001 a0001c0001t0010 a0001c0001t0013 others(37): Show |
273 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(270): Show |
3_prime_UTR_variant | MODIFIER | c.*5dupG | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 6/6 | 6 | INFO_REALIGN_3_PRIME | chr19 | 47741435 | |||||
| chr19:47741512 | C | CGCCCTGC others(2): Show |
1 | a0001c0002t0004 | 15 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*86_*94dupGCCTGCCC others(1): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 6/6 | 95 | INFO_REALIGN_3_PRIME | chr19 | 47741512 | |||||
| chr19:47741537 | C | A | 1 | a0001c0001t0015 | 1 | HG01258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*105C>A | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 6/6 | 105 | chr19 | 47741537 | ||||||
| chr19:47741546 | C | A | 1 | a0005c0017t0014 | 1 | NA19076.hp2 | 3_prime_UTR_variant | MODIFIER | c.*114C>A | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 6/6 | 114 | chr19 | 47741546 | ||||||
| chr19:47741818 | T | C | 4 | a0001c0008t0005 a0001c0010t0005 a0001c0010t0016 others(1): Show |
11 | HG00099.hp2 HG00280.hp1 HG00741.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*386T>C | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 6/6 | 386 | chr19 | 47741818 | ||||||
| chr19:47741832 | G | A | 2 | a0001c0002t0008 a0001c0014t0008 |
5 | HG02486.hp1 HG02965.hp2 HG03098.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*400G>A | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 6/6 | 400 | chr19 | 47741832 | ||||||
| chr19:47741836 | G | T | 1 | a0001c0002t0020 | 1 | HG01928.hp2 | 3_prime_UTR_variant | MODIFIER | c.*404G>T | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 6/6 | 404 | chr19 | 47741836 | ||||||
| chr19:47741851 | C | T | 2 | a0001c0004t0007 a0002c0007t0007 |
8 | HG02145.hp2 HG02630.hp2 HG03041.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*419C>T | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 6/6 | 419 | chr19 | 47741851 | ||||||
| chr19:47741912 | G | A | 3 | a0001c0008t0005 a0001c0010t0005 a0001c0018t0005 |
10 | HG00099.hp2 HG00280.hp1 HG00741.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*480G>A | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 6/6 | 480 | chr19 | 47741912 | ||||||
| chr19:47742143 | CTTTT | C | 11 | a0001c0002t0003 a0001c0002t0004 a0001c0002t0008 others(8): Show |
59 | HG00738.hp1 HG01069.hp1 HG01884.hp1 others(56): Show |
3_prime_UTR_variant | MODIFIER | c.*712_*715delTTTT | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 6/6 | 712 | chr19 | 47742143 | ||||||
| chr19:47742197 | C | T | 1 | a0001c0002t0017 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*765C>T | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 6/6 | 765 | chr19 | 47742197 | ||||||
| chr19:47742277 | C | CCTTT | 23 | a0001c0001t0001 a0001c0001t0010 a0001c0001t0013 others(20): Show |
197 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(194): Show |
3_prime_UTR_variant | MODIFIER | c.*854_*857dupCTTT | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 6/6 | 858 | INFO_REALIGN_3_PRIME | chr19 | 47742277 | |||||
| chr19:47742323 | A | C | 1 | a0001c0001t0010 | 3 | HG03195.hp2 HG03209.hp2 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*891A>C | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 6/6 | 891 | chr19 | 47742323 | ||||||
| chr19:47742523 | T | C | 42 | a0001c0001t0001 a0001c0001t0010 a0001c0001t0013 others(39): Show |
276 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(273): Show |
3_prime_UTR_variant | MODIFIER | c.*1091T>C | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 6/6 | 1091 | chr19 | 47742523 | ||||||
| chr19:47742723 | G | A | 1 | a0001c0001t0018 | 1 | HG04115.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1291G>A | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 6/6 | 1291 | chr19 | 47742723 | ||||||
| chr19:47742935 | T | C | 1 | a0001c0004t0019 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1503T>C | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 6/6 | 1503 | chr19 | 47742935 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:47713664 | C | T | 1 | a0001c0004t0007g0392 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-56+126C>T | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 1/5 | chr19 | 47713664 | |||||||
| chr19:47713678 | G | A | 3 | a0001c0002t0002g0007 a0001c0002t0002g0009 a0001c0003t0002g0008 |
3 | HG01433.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-56+140G>A | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 1/5 | chr19 | 47713678 | |||||||
| chr19:47713725 | C | A | 1 | a0001c0001t0001g0010 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.-56+187C>A | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 1/5 | chr19 | 47713725 | |||||||
| chr19:47713754 | C | T | 37 | a0001c0001t0001g0355 a0001c0001t0001g0356 a0001c0001t0001g0357 others(34): Show |
37 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(34): Show |
intron_variant | MODIFIER | c.-56+216C>T | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 1/5 | chr19 | 47713754 | |||||||
| chr19:47713793 | C | G | 1 | a0001c0001t0001g0354 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.-56+255C>G | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 1/5 | chr19 | 47713793 | |||||||
| chr19:47714007 | C | T | 1 | a0001c0001t0018g0044 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-56+469C>T | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 1/5 | chr19 | 47714007 | |||||||
| chr19:47714285 | G | A | 9 | a0001c0001t0001g0019 a0001c0010t0005g0012 a0001c0010t0005g0015 others(6): Show |
9 | HG00280.hp2 HG01243.hp1 HG01255.hp1 others(6): Show |
intron_variant | MODIFIER | c.-56+747G>A | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 1/5 | chr19 | 47714285 | |||||||
| chr19:47714327 | T | C | 5 | a0001c0001t0001g0024 a0001c0002t0003g0020 a0001c0004t0003g0021 others(2): Show |
5 | HG02109.hp2 HG02818.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.-56+789T>C | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 1/5 | chr19 | 47714327 | |||||||
| chr19:47714431 | CT | C | 5 | a0001c0001t0001g0010 a0001c0001t0001g0355 a0001c0002t0002g0007 others(2): Show |
5 | HG02280.hp1 HG02897.hp1 NA18940.hp2 others(2): Show |
intron_variant | MODIFIER | c.-56+899delT | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr19 | 47714431 | ||||||
| chr19:47714458 | C | G | 12 | a0001c0001t0001g0347 a0001c0001t0010g0344 a0001c0001t0010g0350 others(9): Show |
13 | HG00738.hp1 HG02145.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.-56+920C>G | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 1/5 | chr19 | 47714458 | |||||||
| chr19:47714507 | C | T | 5 | a0001c0002t0009g0338 a0001c0003t0002g0339 a0001c0003t0002g0340 others(2): Show |
5 | HG01346.hp2 HG02738.hp2 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.-56+969C>T | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 1/5 | chr19 | 47714507 | |||||||
| chr19:47714581 | G | A | 1 | a0001c0002t0003g0027 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-56+1043G>A | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 1/5 | chr19 | 47714581 | |||||||
| chr19:47714625 | G | A | 1 | a0001c0001t0001g0028 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-56+1087G>A | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 1/5 | chr19 | 47714625 | |||||||
| chr19:47714643 | T | C | 1 | a0001c0004t0009g0029 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-56+1105T>C | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 1/5 | chr19 | 47714643 | |||||||
| chr19:47714682 | C | T | 92 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0303 others(89): Show |
97 | HG00280.hp2 HG00639.hp1 HG00735.hp2 others(94): Show |
intron_variant | MODIFIER | c.-56+1144C>T | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 1/5 | chr19 | 47714682 | |||||||
| chr19:47714688 | A | C | 41 | a0001c0001t0001g0010 a0001c0001t0001g0303 a0001c0001t0001g0309 others(38): Show |
44 | HG00639.hp1 HG00735.hp2 HG01070.hp2 others(41): Show |
intron_variant | MODIFIER | c.-56+1150A>C | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 1/5 | chr19 | 47714688 | |||||||
| chr19:47714756 | C | G | 1 | a0002c0009t0001g0280 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-56+1218C>G | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 1/5 | chr19 | 47714756 | |||||||
| chr19:47714758 | G | A | 2 | a0001c0002t0003g0301 a0001c0015t0001g0302 |
2 | HG01074.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.-56+1220G>A | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 1/5 | chr19 | 47714758 | |||||||
| chr19:47714896 | G | A | 1 | a0001c0002t0004g0281 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-56+1358G>A | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 1/5 | chr19 | 47714896 | |||||||
| chr19:47715009 | G | C | 2 | a0001c0002t0009g0338 a0001c0003t0002g0339 |
2 | NA18522.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-56+1471G>C | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 1/5 | chr19 | 47715009 | |||||||
| chr19:47715024 | T | C | 46 | a0001c0001t0001g0019 a0001c0001t0010g0300 a0001c0002t0002g0036 others(43): Show |
47 | HG00280.hp2 HG01243.hp1 HG01255.hp1 others(44): Show |
intron_variant | MODIFIER | c.-56+1486T>C | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 1/5 | chr19 | 47715024 | |||||||
| chr19:47715038 | C | CAAAT | 80 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0001t0001g0153 others(77): Show |
81 | HG00323.hp2 HG00621.hp2 HG00738.hp1 others(78): Show |
intron_variant | MODIFIER | c.-55-1480_-55-1477d others(6): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr19 | 47715038 | ||||||
| chr19:47715038 | C | CAAATAAA others(1): Show |
72 | a0001c0001t0001g0208 a0001c0001t0001g0211 a0001c0001t0001g0215 others(69): Show |
73 | HG00558.hp1 HG00558.hp2 HG00639.hp2 others(70): Show |
intron_variant | MODIFIER | c.-55-1484_-55-1477d others(10): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr19 | 47715038 | ||||||
| chr19:47715038 | C | CAAATAAA others(5): Show |
5 | a0001c0001t0001g0274 a0001c0001t0001g0277 a0001c0002t0002g0273 others(2): Show |
5 | HG02074.hp1 HG02135.hp2 HG02300.hp1 others(2): Show |
intron_variant | MODIFIER | c.-55-1488_-55-1477d others(14): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr19 | 47715038 | ||||||
| chr19:47715038 | C | CAAATAAA others(9): Show |
2 | a0001c0001t0001g0279 a0001c0002t0002g0278 |
2 | HG01168.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.-55-1492_-55-1477d others(18): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr19 | 47715038 | ||||||
| chr19:47715038 | CAAAT | C | 108 | a0001c0001t0001g0010 a0001c0001t0001g0024 a0001c0001t0001g0046 others(105): Show |
111 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.-55-1480_-55-1477d others(6): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr19 | 47715038 | ||||||
| chr19:47715038 | CAAATAAA others(1): Show |
C | 14 | a0001c0001t0001g0019 a0001c0002t0003g0030 a0001c0002t0003g0031 others(11): Show |
14 | HG00280.hp2 HG01243.hp1 HG01255.hp1 others(11): Show |
intron_variant | MODIFIER | c.-55-1484_-55-1477d others(10): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr19 | 47715038 | ||||||
| chr19:47715038 | CAAATAAA others(5): Show |
C | 1 | a0001c0001t0001g0356 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-55-1488_-55-1477d others(14): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr19 | 47715038 | ||||||
| chr19:47715038 | CAAATAAA others(9): Show |
C | 2 | a0001c0002t0003g0027 a0001c0002t0003g0282 |
2 | HG02809.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-55-1492_-55-1477d others(18): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr19 | 47715038 | ||||||
| chr19:47715078 | T | TAAATAAA others(5): Show |
1 | a0001c0001t0001g0207 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-55-1477_-55-1476i others(14): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr19 | 47715078 | ||||||
| chr19:47715082 | A | T | 1 | a0001c0004t0007g0392 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-55-1476A>T | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 1/5 | chr19 | 47715082 | |||||||
| chr19:47715155 | G | A | 3 | a0001c0003t0002g0340 a0001c0008t0005g0341 a0002c0007t0007g0342 |
3 | HG01346.hp2 HG02738.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-55-1403G>A | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 1/5 | chr19 | 47715155 | |||||||
| chr19:47715268 | C | T | 135 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0165 others(132): Show |
136 | HG00558.hp1 HG00558.hp2 HG00621.hp2 others(133): Show |
intron_variant | MODIFIER | c.-55-1290C>T | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 1/5 | chr19 | 47715268 | |||||||
| chr19:47715639 | C | T | 6 | a0001c0001t0010g0300 a0001c0002t0003g0288 a0001c0002t0003g0289 others(3): Show |
6 | HG01884.hp2 HG02976.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.-55-919C>T | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 1/5 | chr19 | 47715639 | |||||||
| chr19:47715640 | G | A | 30 | a0001c0001t0001g0165 a0001c0001t0001g0169 a0001c0001t0001g0215 others(27): Show |
30 | HG00642.hp2 HG01928.hp1 HG01975.hp1 others(27): Show |
intron_variant | MODIFIER | c.-55-918G>A | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 1/5 | chr19 | 47715640 | |||||||
| chr19:47715640 | G | C | 2 | a0001c0002t0003g0030 a0001c0002t0003g0031 |
2 | HG02055.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-55-918G>C | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 1/5 | chr19 | 47715640 | |||||||
| chr19:47715643 | T | A | 1 | a0001c0001t0001g0355 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.-55-915T>A | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 1/5 | chr19 | 47715643 | |||||||
| chr19:47715682 | G | A | 1 | a0001c0001t0001g0222 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-55-876G>A | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 1/5 | chr19 | 47715682 | |||||||
| chr19:47715747 | A | G | 1 | a0001c0001t0001g0010 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.-55-811A>G | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 1/5 | chr19 | 47715747 | |||||||
| chr19:47715772 | C | T | 1 | a0001c0004t0007g0392 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-55-786C>T | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 1/5 | chr19 | 47715772 | |||||||
| chr19:47715842 | A | C | 1 | a0001c0004t0006g0272 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-55-716A>C | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 1/5 | chr19 | 47715842 | |||||||
| chr19:47715924 | G | C | 160 | a0001c0001t0001g0010 a0001c0001t0001g0024 a0001c0001t0001g0144 others(157): Show |
165 | HG00639.hp1 HG00639.hp2 HG00642.hp1 others(162): Show |
intron_variant | MODIFIER | c.-55-634G>C | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 1/5 | chr19 | 47715924 | |||||||
| chr19:47715995 | C | A | 1 | a0001c0003t0002g0039 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-55-563C>A | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 1/5 | chr19 | 47715995 | |||||||
| chr19:47716068 | C | CT | 52 | a0001c0001t0001g0010 a0001c0001t0001g0066 a0001c0001t0001g0068 others(49): Show |
54 | HG00544.hp2 HG00639.hp1 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.-55-469dupT | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr19 | 47716068 | ||||||
| chr19:47716068 | C | CTT | 10 | a0001c0001t0001g0325 a0001c0001t0001g0328 a0001c0002t0002g0322 others(7): Show |
10 | HG01169.hp1 HG01175.hp2 HG01361.hp2 others(7): Show |
intron_variant | MODIFIER | c.-55-470_-55-469dup others(2): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr19 | 47716068 | ||||||
| chr19:47716068 | CT | C | 67 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0075 others(64): Show |
67 | HG00639.hp2 HG00642.hp2 HG00738.hp2 others(64): Show |
intron_variant | MODIFIER | c.-55-469delT | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr19 | 47716068 | ||||||
| chr19:47716068 | CTT | C | 14 | a0001c0001t0001g0024 a0001c0001t0001g0303 a0001c0001t0010g0300 others(11): Show |
15 | HG01243.hp2 HG01884.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.-55-470_-55-469del others(2): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr19 | 47716068 | ||||||
| chr19:47716100 | C | G | 1 | a0001c0002t0002g0001 | 2 | NA18957.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.-55-458C>G | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 1/5 | chr19 | 47716100 | |||||||
| chr19:47716167 | C | G | 1 | a0001c0004t0003g0183 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-55-391C>G | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 1/5 | chr19 | 47716167 | |||||||
| chr19:47716379 | A | G | 1 | a0001c0001t0001g0267 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-55-179A>G | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 1/5 | chr19 | 47716379 | |||||||
| chr19:47716415 | CTGTGACC others(7): Show |
C | 9 | a0001c0001t0001g0024 a0001c0001t0001g0303 a0001c0002t0003g0292 others(6): Show |
10 | HG01074.hp2 HG01243.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.-55-132_-55-119del others(14): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr19 | 47716415 | ||||||
| chr19:47716539 | C | A | 1 | a0001c0002t0002g0227 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-55-19C>A | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 1/5 | chr19 | 47716539 | |||||||
| chr19:47717466 | C | T | 49 | a0001c0001t0001g0309 a0001c0001t0001g0311 a0001c0001t0001g0313 others(46): Show |
51 | HG00639.hp1 HG00642.hp1 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.404+450C>T | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 2/5 | chr19 | 47717466 | |||||||
| chr19:47717712 | G | C | 1 | a0001c0001t0001g0357 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.404+696G>C | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 2/5 | chr19 | 47717712 | |||||||
| chr19:47717736 | G | A | 58 | a0001c0001t0001g0010 a0001c0001t0001g0144 a0001c0001t0001g0145 others(55): Show |
59 | HG00642.hp2 HG00738.hp2 HG01069.hp1 others(56): Show |
intron_variant | MODIFIER | c.404+720G>A | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 2/5 | chr19 | 47717736 | |||||||
| chr19:47717778 | C | T | 6 | a0001c0001t0013g0072 a0001c0002t0003g0020 a0001c0002t0004g0281 others(3): Show |
6 | HG02109.hp2 HG02723.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.405-731C>T | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 2/5 | chr19 | 47717778 | |||||||
| chr19:47717779 | G | C | 52 | a0001c0001t0001g0010 a0001c0001t0001g0144 a0001c0001t0001g0145 others(49): Show |
52 | HG00642.hp2 HG00738.hp2 HG01069.hp1 others(49): Show |
intron_variant | MODIFIER | c.405-730G>C | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 2/5 | chr19 | 47717779 | |||||||
| chr19:47717811 | G | A | 1 | a0001c0001t0001g0356 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.405-698G>A | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 2/5 | chr19 | 47717811 | |||||||
| chr19:47717906 | T | TA | 30 | a0001c0001t0001g0010 a0001c0001t0001g0066 a0001c0001t0001g0078 others(27): Show |
30 | HG00438.hp1 HG00544.hp1 HG00621.hp1 others(27): Show |
intron_variant | MODIFIER | c.405-582dupA | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr19 | 47717906 | ||||||
| chr19:47717906 | TA | T | 90 | a0001c0001t0001g0024 a0001c0001t0001g0266 a0001c0001t0001g0279 others(87): Show |
94 | HG00639.hp1 HG00642.hp1 HG00735.hp2 others(91): Show |
intron_variant | MODIFIER | c.405-582delA | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr19 | 47717906 | ||||||
| chr19:47718001 | A | C | 3 | a0001c0010t0005g0017 a0001c0010t0005g0284 a0001c0028t0001g0283 |
3 | HG01243.hp1 HG02683.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.405-508A>C | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 2/5 | chr19 | 47718001 | |||||||
| chr19:47718005 | T | C | 1 | a0001c0001t0001g0024 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.405-504T>C | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 2/5 | chr19 | 47718005 | |||||||
| chr19:47718011 | G | A | 2 | a0001c0002t0002g0007 a0001c0002t0002g0009 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.405-498G>A | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 2/5 | chr19 | 47718011 | |||||||
| chr19:47718058 | A | G | 1 | a0001c0002t0004g0299 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.405-451A>G | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 2/5 | chr19 | 47718058 | |||||||
| chr19:47718101 | C | T | 20 | a0001c0001t0001g0024 a0001c0001t0001g0337 a0001c0001t0001g0347 others(17): Show |
20 | HG01074.hp2 HG02145.hp2 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.405-408C>T | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 2/5 | chr19 | 47718101 | |||||||
| chr19:47718127 | G | C | 10 | a0001c0002t0002g0171 a0001c0002t0003g0287 a0001c0002t0003g0294 others(7): Show |
11 | HG02280.hp2 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.405-382G>C | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 2/5 | chr19 | 47718127 | |||||||
| chr19:47718135 | A | T | 153 | a0001c0001t0001g0010 a0001c0001t0001g0024 a0001c0001t0001g0144 others(150): Show |
158 | HG00639.hp1 HG00642.hp1 HG00642.hp2 others(155): Show |
intron_variant | MODIFIER | c.405-374A>T | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 2/5 | chr19 | 47718135 | |||||||
| chr19:47718273 | C | CA | 113 | a0001c0001t0001g0010 a0001c0001t0001g0066 a0001c0001t0001g0078 others(110): Show |
117 | HG00140.hp1 HG00639.hp1 HG00642.hp2 others(114): Show |
intron_variant | MODIFIER | c.405-216dupA | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr19 | 47718273 | ||||||
| chr19:47718273 | C | CAA | 11 | a0001c0001t0001g0215 a0001c0001t0001g0303 a0001c0001t0013g0072 others(8): Show |
11 | HG00642.hp1 HG01175.hp2 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.405-217_405-216dup others(2): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr19 | 47718273 | ||||||
| chr19:47718273 | CA | C | 19 | a0001c0001t0001g0024 a0001c0001t0001g0388 a0001c0002t0002g0069 others(16): Show |
19 | HG01074.hp2 HG01256.hp1 HG01515.hp2 others(16): Show |
intron_variant | MODIFIER | c.405-216delA | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr19 | 47718273 | ||||||
| chr19:47718384 | C | T | 1 | a0001c0001t0001g0028 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.405-125C>T | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 2/5 | chr19 | 47718384 | |||||||
| chr19:47718397 | C | T | 15 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0001g0389 others(12): Show |
16 | HG02040.hp2 HG02451.hp2 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.405-112C>T | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 2/5 | chr19 | 47718397 | |||||||
| chr19:47718452 | G | A | 27 | a0001c0001t0001g0337 a0001c0001t0001g0347 a0001c0001t0010g0300 others(24): Show |
28 | HG01884.hp2 HG02040.hp2 HG02145.hp2 others(25): Show |
intron_variant | MODIFIER | c.405-57G>A | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 2/5 | chr19 | 47718452 | |||||||
| chr19:47718626 | G | GGGGTCTG others(280): Show |
1 | a0001c0002t0003g0070 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.502+45_502+46insGC others(285): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr19 | 47718626 | ||||||
| chr19:47718648 | GGGGCCTG others(63): Show |
G | 1 | a0001c0004t0009g0029 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.502+46_502+115delC others(69): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr19 | 47718648 | ||||||
| chr19:47718667 | C | T | 1 | a0001c0001t0001g0050 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.502+61C>T | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | chr19 | 47718667 | |||||||
| chr19:47718681 | A | G | 32 | a0001c0001t0001g0024 a0001c0001t0001g0337 a0001c0001t0001g0347 others(29): Show |
33 | HG01074.hp2 HG01081.hp2 HG02040.hp2 others(30): Show |
intron_variant | MODIFIER | c.502+75A>G | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | chr19 | 47718681 | |||||||
| chr19:47718683 | T | TG | 23 | a0001c0001t0001g0024 a0001c0001t0001g0337 a0001c0001t0001g0347 others(20): Show |
24 | HG01074.hp2 HG02145.hp2 HG02257.hp2 others(21): Show |
intron_variant | MODIFIER | c.502+80dupG | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr19 | 47718683 | ||||||
| chr19:47718683 | T | TGGGGCCT others(101): Show |
3 | a0001c0002t0006g0033 a0002c0007t0003g0032 a0002c0007t0006g0034 |
3 | HG02622.hp1 HG02818.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.502+80_502+81insGC others(106): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr19 | 47718683 | ||||||
| chr19:47718683 | T | TGGGGTCT others(173): Show |
1 | a0001c0001t0001g0373 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.502+80_502+81insGT others(178): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr19 | 47718683 | ||||||
| chr19:47718687 | C | T | 1 | a0001c0001t0001g0373 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.502+81C>T | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | chr19 | 47718687 | |||||||
| chr19:47718689 | C | CGGACTCC others(29): Show |
104 | a0001c0001t0001g0019 a0001c0001t0001g0028 a0001c0001t0001g0061 others(101): Show |
105 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.502+130_502+165dup others(36): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr19 | 47718689 | ||||||
| chr19:47718689 | C | CGGACTCC others(101): Show |
1 | a0001c0001t0001g0235 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.502+165_502+166ins others(108): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr19 | 47718689 | ||||||
| chr19:47718689 | C | CGGACTCC others(138): Show |
5 | a0001c0001t0001g0207 a0001c0001t0001g0242 a0001c0001t0001g0279 others(2): Show |
5 | HG01168.hp1 HG01952.hp2 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.502+165_502+166ins others(145): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr19 | 47718689 | ||||||
| chr19:47718689 | C | T | 27 | a0001c0001t0001g0024 a0001c0001t0001g0337 a0001c0001t0001g0347 others(24): Show |
28 | HG01074.hp2 HG01081.hp2 HG02145.hp2 others(25): Show |
intron_variant | MODIFIER | c.502+83C>T | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | chr19 | 47718689 | |||||||
| chr19:47718689 | CGGACTCC others(29): Show |
C | 6 | a0001c0004t0003g0021 a0001c0004t0006g0272 a0001c0004t0019g0023 others(3): Show |
6 | HG02109.hp2 HG02559.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.502+130_502+165del others(36): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr19 | 47718689 | ||||||
| chr19:47718690 | GGACTCCT others(100): Show |
G | 1 | a0001c0002t0004g0038 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.502+117_502+223del | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr19 | 47718690 | ||||||
| chr19:47718694 | T | TCCTGGGT others(30): Show |
1 | a0001c0001t0001g0355 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.502+90_502+126dupC others(36): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr19 | 47718694 | ||||||
| chr19:47718715 | GGCTGGGG others(173): Show |
G | 1 | a0001c0002t0002g0124 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.502+117_502+296del | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr19 | 47718715 | ||||||
| chr19:47718716 | G | A | 1 | a0001c0002t0003g0027 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.502+110G>A | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | chr19 | 47718716 | |||||||
| chr19:47718716 | G | GCTGGGGT others(101): Show |
4 | a0001c0002t0003g0020 a0001c0002t0003g0030 a0001c0002t0003g0031 others(1): Show |
4 | HG01891.hp2 HG02055.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.502+129_502+130ins others(108): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr19 | 47718716 | ||||||
| chr19:47718716 | G | GCTGGGGT others(137): Show |
1 | a0001c0002t0004g0281 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.502+145_502+288dup others(144): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr19 | 47718716 | ||||||
| chr19:47718718 | T | TG | 4 | a0001c0002t0002g0171 a0001c0002t0002g0305 a0001c0002t0004g0172 others(1): Show |
4 | HG02040.hp2 HG02572.hp2 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.502+116dupG | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr19 | 47718718 | ||||||
| chr19:47718718 | TG | T | 23 | a0001c0001t0001g0024 a0001c0001t0001g0337 a0001c0001t0001g0347 others(20): Show |
24 | HG01074.hp2 HG02145.hp2 HG02257.hp2 others(21): Show |
intron_variant | MODIFIER | c.502+116delG | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr19 | 47718718 | ||||||
| chr19:47718723 | T | C | 40 | a0001c0001t0001g0024 a0001c0001t0001g0337 a0001c0001t0001g0347 others(37): Show |
41 | HG01074.hp2 HG01243.hp1 HG01255.hp1 others(38): Show |
intron_variant | MODIFIER | c.502+117T>C | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | chr19 | 47718723 | |||||||
| chr19:47718725 | T | C | 22 | a0001c0001t0001g0024 a0001c0001t0001g0337 a0001c0001t0001g0347 others(19): Show |
23 | HG01074.hp2 HG02145.hp2 HG02257.hp2 others(20): Show |
intron_variant | MODIFIER | c.502+119T>C | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | chr19 | 47718725 | |||||||
| chr19:47718725 | T | TGGACTCC others(28): Show |
9 | a0001c0010t0005g0012 a0001c0010t0005g0015 a0001c0010t0005g0017 others(6): Show |
9 | HG01243.hp1 HG01255.hp1 HG01256.hp2 others(6): Show |
intron_variant | MODIFIER | c.502+145_502+146ins others(35): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr19 | 47718725 | ||||||
| chr19:47718736 | G | A | 1 | a0001c0004t0003g0022 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.502+130G>A | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | chr19 | 47718736 | |||||||
| chr19:47718751 | G | A | 1 | a0001c0002t0003g0027 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.502+145G>A | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | chr19 | 47718751 | |||||||
| chr19:47718752 | G | A | 5 | a0001c0002t0002g0171 a0001c0002t0002g0305 a0001c0002t0002g0322 others(2): Show |
5 | HG02040.hp2 HG02523.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.502+146G>A | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | chr19 | 47718752 | |||||||
| chr19:47718754 | T | TG | 22 | a0001c0001t0001g0024 a0001c0001t0001g0337 a0001c0001t0001g0347 others(19): Show |
23 | HG01074.hp2 HG02145.hp2 HG02257.hp2 others(20): Show |
intron_variant | MODIFIER | c.502+152dupG | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr19 | 47718754 | ||||||
| chr19:47718759 | T | C | 28 | a0001c0001t0001g0024 a0001c0001t0001g0337 a0001c0001t0001g0347 others(25): Show |
29 | HG01074.hp2 HG02145.hp2 HG02257.hp2 others(26): Show |
intron_variant | MODIFIER | c.502+153T>C | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | chr19 | 47718759 | |||||||
| chr19:47718761 | T | C | 1 | a0001c0004t0003g0022 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.502+155T>C | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | chr19 | 47718761 | |||||||
| chr19:47718772 | A | G | 38 | a0001c0001t0001g0024 a0001c0001t0001g0062 a0001c0001t0001g0202 others(35): Show |
39 | HG01074.hp2 HG01934.hp1 HG02040.hp2 others(36): Show |
intron_variant | MODIFIER | c.502+166A>G | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | chr19 | 47718772 | |||||||
| chr19:47718772 | ATCTGAGG others(28): Show |
A | 1 | a0001c0004t0007g0065 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.502+188_502+222del others(35): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr19 | 47718772 | ||||||
| chr19:47718787 | G | A | 4 | a0001c0002t0002g0171 a0001c0002t0002g0322 a0001c0002t0004g0172 others(1): Show |
4 | HG02040.hp2 HG02523.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.502+181G>A | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | chr19 | 47718787 | |||||||
| chr19:47718788 | G | A | 22 | a0001c0001t0001g0024 a0001c0001t0001g0337 a0001c0001t0001g0347 others(19): Show |
23 | HG01074.hp2 HG02145.hp2 HG02257.hp2 others(20): Show |
intron_variant | MODIFIER | c.502+182G>A | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | chr19 | 47718788 | |||||||
| chr19:47718790 | T | TG | 28 | a0001c0001t0001g0024 a0001c0001t0001g0062 a0001c0001t0001g0336 others(25): Show |
29 | HG01074.hp2 HG01934.hp1 HG02040.hp2 others(26): Show |
intron_variant | MODIFIER | c.502+187dupG | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr19 | 47718790 | ||||||
| chr19:47718791 | GGGCCCAG others(64): Show |
G | 1 | a0001c0002t0003g0027 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.502+188_502+258del others(71): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr19 | 47718791 | ||||||
| chr19:47718794 | C | T | 25 | a0001c0001t0001g0024 a0001c0001t0001g0062 a0001c0001t0001g0336 others(22): Show |
26 | HG01074.hp2 HG01934.hp1 HG02145.hp2 others(23): Show |
intron_variant | MODIFIER | c.502+188C>T | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | chr19 | 47718794 | |||||||
| chr19:47718796 | C | T | 30 | a0001c0001t0001g0024 a0001c0001t0001g0062 a0001c0001t0001g0336 others(27): Show |
31 | HG01074.hp2 HG01934.hp1 HG02040.hp2 others(28): Show |
intron_variant | MODIFIER | c.502+190C>T | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | chr19 | 47718796 | |||||||
| chr19:47718797 | A | AGACTCCT others(67): Show |
1 | a0001c0002t0002g0245 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.502+253_502+254ins others(74): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr19 | 47718797 | ||||||
| chr19:47718797 | A | G | 35 | a0001c0001t0001g0024 a0001c0001t0001g0062 a0001c0001t0001g0080 others(32): Show |
36 | HG00621.hp1 HG01074.hp2 HG01934.hp1 others(33): Show |
intron_variant | MODIFIER | c.502+191A>G | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | chr19 | 47718797 | |||||||
| chr19:47718807 | G | A | 2 | a0001c0001t0001g0062 a0001c0002t0002g0137 |
2 | HG02602.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.502+201G>A | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | chr19 | 47718807 | |||||||
| chr19:47718816 | AG | A | 4 | a0001c0002t0002g0171 a0001c0002t0002g0322 a0001c0002t0004g0172 others(1): Show |
4 | HG02040.hp2 HG02523.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.502+212delG | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr19 | 47718816 | ||||||
| chr19:47718822 | G | A | 22 | a0001c0001t0001g0024 a0001c0001t0001g0337 a0001c0001t0001g0347 others(19): Show |
23 | HG01074.hp2 HG02145.hp2 HG02257.hp2 others(20): Show |
intron_variant | MODIFIER | c.502+216G>A | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | chr19 | 47718822 | |||||||
| chr19:47718823 | G | A | 1 | a0001c0004t0003g0022 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.502+217G>A | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | chr19 | 47718823 | |||||||
| chr19:47718825 | TG | T | 23 | a0001c0001t0001g0024 a0001c0001t0001g0337 a0001c0001t0001g0347 others(20): Show |
24 | HG01074.hp2 HG02145.hp2 HG02257.hp2 others(21): Show |
intron_variant | MODIFIER | c.502+224delG | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr19 | 47718825 | ||||||
| chr19:47718827 | GGGGCCTG others(99): Show |
G | 1 | a0001c0004t0009g0029 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.502+246_502+351del | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr19 | 47718827 | ||||||
| chr19:47718831 | C | T | 2 | a0001c0002t0002g0305 a0001c0004t0003g0022 |
2 | HG03139.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.502+225C>T | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | chr19 | 47718831 | |||||||
| chr19:47718831 | CCTGGACT others(29): Show |
C | 1 | a0001c0001t0001g0211 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.502+253_502+288del others(36): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr19 | 47718831 | ||||||
| chr19:47718833 | T | C | 2 | a0001c0001t0001g0062 a0001c0002t0002g0137 |
2 | HG02602.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.502+227T>C | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | chr19 | 47718833 | |||||||
| chr19:47718834 | G | A | 2 | a0001c0001t0001g0062 a0001c0002t0002g0137 |
2 | HG02602.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.502+228G>A | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | chr19 | 47718834 | |||||||
| chr19:47718851 | G | A | 4 | a0001c0002t0002g0171 a0001c0002t0002g0322 a0001c0002t0004g0172 others(1): Show |
4 | HG02040.hp2 HG02523.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.502+245G>A | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | chr19 | 47718851 | |||||||
| chr19:47718853 | AG | A | 22 | a0001c0001t0001g0024 a0001c0001t0001g0337 a0001c0001t0001g0347 others(19): Show |
23 | HG01074.hp2 HG02145.hp2 HG02257.hp2 others(20): Show |
intron_variant | MODIFIER | c.502+249delG | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr19 | 47718853 | ||||||
| chr19:47718854 | GGAGGGAC others(64): Show |
G | 2 | a0001c0002t0002g0322 a0001c0004t0002g0043 |
2 | HG02040.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.502+254_502+324del others(71): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr19 | 47718854 | ||||||
| chr19:47718859 | G | A | 1 | a0001c0002t0002g0305 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.502+253G>A | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | chr19 | 47718859 | |||||||
| chr19:47718860 | A | G | 28 | a0001c0001t0001g0024 a0001c0001t0001g0062 a0001c0001t0001g0337 others(25): Show |
29 | HG01074.hp2 HG02145.hp2 HG02257.hp2 others(26): Show |
intron_variant | MODIFIER | c.502+254A>G | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | chr19 | 47718860 | |||||||
| chr19:47718862 | T | TG | 25 | a0001c0001t0001g0024 a0001c0001t0001g0062 a0001c0001t0001g0337 others(22): Show |
26 | HG01074.hp2 HG02145.hp2 HG02257.hp2 others(23): Show |
intron_variant | MODIFIER | c.502+260dupG | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr19 | 47718862 | ||||||
| chr19:47718862 | TGGGGTCT others(30): Show |
T | 2 | a0001c0002t0002g0171 a0001c0002t0004g0172 |
2 | HG02572.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.502+260_502+296del others(37): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr19 | 47718862 | ||||||
| chr19:47718864 | G | T | 1 | a0001c0002t0002g0263 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.502+258G>T | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | chr19 | 47718864 | |||||||
| chr19:47718867 | T | C | 27 | a0001c0001t0001g0024 a0001c0001t0001g0062 a0001c0001t0001g0337 others(24): Show |
28 | HG01074.hp2 HG02145.hp2 HG02257.hp2 others(25): Show |
intron_variant | MODIFIER | c.502+261T>C | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | chr19 | 47718867 | |||||||
| chr19:47718887 | G | A | 23 | a0001c0001t0001g0024 a0001c0001t0001g0337 a0001c0001t0001g0347 others(20): Show |
24 | HG01074.hp2 HG02145.hp2 HG02257.hp2 others(21): Show |
intron_variant | MODIFIER | c.502+281G>A | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | chr19 | 47718887 | |||||||
| chr19:47718895 | A | G | 26 | a0001c0001t0001g0024 a0001c0001t0001g0062 a0001c0001t0001g0337 others(23): Show |
27 | HG01074.hp2 HG02145.hp2 HG02257.hp2 others(24): Show |
intron_variant | MODIFIER | c.502+289A>G | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | chr19 | 47718895 | |||||||
| chr19:47718896 | G | A | 2 | a0001c0001t0001g0062 a0001c0002t0002g0137 |
2 | HG02602.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.502+290G>A | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | chr19 | 47718896 | |||||||
| chr19:47718898 | TG | T | 23 | a0001c0001t0001g0024 a0001c0001t0001g0337 a0001c0001t0001g0347 others(20): Show |
24 | HG01074.hp2 HG02145.hp2 HG02257.hp2 others(21): Show |
intron_variant | MODIFIER | c.502+296delG | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr19 | 47718898 | ||||||
| chr19:47718899 | G | GGGGCCTG others(64): Show |
3 | a0001c0002t0006g0033 a0002c0007t0003g0032 a0002c0007t0006g0034 |
3 | HG02622.hp1 HG02818.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.502+330_502+331ins others(71): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr19 | 47718899 | ||||||
| chr19:47718899 | G | GGGGCCTG others(28): Show |
3 | a0001c0001t0001g0334 a0001c0001t0001g0336 a0001c0002t0002g0335 |
3 | HG01109.hp1 HG01934.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.502+320_502+321ins others(35): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr19 | 47718899 | ||||||
| chr19:47718903 | C | T | 2 | a0001c0001t0001g0062 a0001c0002t0002g0137 |
2 | HG02602.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.502+297C>T | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | chr19 | 47718903 | |||||||
| chr19:47718923 | G | A | 3 | a0001c0002t0002g0305 a0001c0002t0003g0282 a0001c0004t0003g0183 |
3 | HG01891.hp2 HG02922.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.502+317G>A | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | chr19 | 47718923 | |||||||
| chr19:47718925 | A | AG | 5 | a0001c0001t0001g0062 a0001c0002t0002g0137 a0001c0002t0002g0305 others(2): Show |
5 | HG01891.hp2 HG02602.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.502+320dupG | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr19 | 47718925 | ||||||
| chr19:47718930 | G | A | 2 | a0001c0001t0001g0062 a0001c0002t0002g0137 |
2 | HG02602.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.502+324G>A | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | chr19 | 47718930 | |||||||
| chr19:47719104 | T | C | 2 | a0001c0002t0004g0297 a0001c0002t0017g0298 |
2 | HG03225.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.502+498T>C | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | chr19 | 47719104 | |||||||
| chr19:47719128 | G | A | 1 | a0001c0002t0002g0234 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.502+522G>A | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | chr19 | 47719128 | |||||||
| chr19:47719179 | G | A | 2 | a0001c0002t0002g0204 a0001c0002t0002g0264 |
2 | HG01256.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.502+573G>A | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | chr19 | 47719179 | |||||||
| chr19:47719232 | G | A | 2 | a0001c0001t0001g0084 a0001c0001t0001g0208 |
2 | HG01106.hp1 HG01167.hp2 |
intron_variant | MODIFIER | c.502+626G>A | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | chr19 | 47719232 | |||||||
| chr19:47719347 | G | A | 4 | a0001c0002t0002g0333 a0001c0002t0004g0330 a0001c0002t0004g0331 others(1): Show |
4 | HG01884.hp1 HG02615.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.502+741G>A | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | chr19 | 47719347 | |||||||
| chr19:47719449 | C | T | 7 | a0001c0002t0004g0038 a0001c0002t0004g0064 a0001c0002t0004g0146 others(4): Show |
7 | HG01891.hp1 HG02055.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.502+843C>T | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | chr19 | 47719449 | |||||||
| chr19:47719458 | C | T | 1 | a0001c0002t0003g0320 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.502+852C>T | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | chr19 | 47719458 | |||||||
| chr19:47719617 | G | A | 1 | a0001c0004t0009g0029 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.502+1011G>A | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | chr19 | 47719617 | |||||||
| chr19:47719769 | C | T | 1 | a0001c0002t0002g0069 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.502+1163C>T | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | chr19 | 47719769 | |||||||
| chr19:47719851 | G | C | 1 | a0001c0001t0001g0359 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.502+1245G>C | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | chr19 | 47719851 | |||||||
| chr19:47719933 | T | C | 1 | a0006c0021t0001g0085 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.502+1327T>C | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | chr19 | 47719933 | |||||||
| chr19:47719944 | A | ATGTGTGT others(1): Show |
20 | a0001c0001t0001g0309 a0001c0001t0001g0311 a0001c0001t0001g0313 others(17): Show |
21 | HG00639.hp1 HG00735.hp2 HG00738.hp1 others(18): Show |
intron_variant | MODIFIER | c.502+1339_502+1340i others(10): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr19 | 47719944 | ||||||
| chr19:47719944 | A | ATGTGTGT others(3): Show |
3 | a0001c0002t0002g0318 a0001c0002t0002g0319 a0001c0003t0002g0339 |
3 | HG02717.hp2 HG02886.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.502+1339_502+1340i others(12): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr19 | 47719944 | ||||||
| chr19:47719946 | A | ATG | 44 | a0001c0001t0001g0019 a0001c0001t0001g0028 a0001c0001t0001g0061 others(41): Show |
45 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(42): Show |
intron_variant | MODIFIER | c.502+1363_502+1364d others(4): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr19 | 47719946 | ||||||
| chr19:47719946 | A | ATGTG | 22 | a0001c0001t0001g0076 a0001c0001t0001g0136 a0001c0001t0013g0072 others(19): Show |
22 | HG01243.hp1 HG01255.hp1 HG01256.hp2 others(19): Show |
intron_variant | MODIFIER | c.502+1361_502+1364d others(6): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr19 | 47719946 | ||||||
| chr19:47719946 | A | ATGTGTG | 7 | a0001c0001t0001g0303 a0001c0002t0006g0003 a0001c0002t0006g0026 others(4): Show |
8 | HG01243.hp2 HG02258.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.502+1359_502+1364d others(8): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr19 | 47719946 | ||||||
| chr19:47719946 | A | ATGTGTGT others(1): Show |
61 | a0001c0001t0001g0010 a0001c0001t0001g0144 a0001c0001t0001g0145 others(58): Show |
61 | HG00642.hp2 HG00738.hp2 HG01069.hp1 others(58): Show |
intron_variant | MODIFIER | c.502+1357_502+1364d others(10): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr19 | 47719946 | ||||||
| chr19:47719946 | A | ATGTGTGT others(3): Show |
3 | a0001c0002t0002g0036 a0001c0002t0003g0352 a0001c0002t0003g0353 |
3 | HG01261.hp2 HG02622.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.502+1355_502+1364d others(12): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr19 | 47719946 | ||||||
| chr19:47719946 | A | ATGTGTGT others(5): Show |
7 | a0001c0002t0003g0004 a0001c0002t0003g0306 a0001c0002t0003g0307 others(4): Show |
8 | HG01074.hp2 HG02809.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.502+1353_502+1364d others(14): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr19 | 47719946 | ||||||
| chr19:47719946 | A | ATGTGTGT others(7): Show |
5 | a0001c0001t0001g0024 a0001c0002t0003g0225 a0001c0002t0003g0292 others(2): Show |
5 | HG01891.hp2 HG02280.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.502+1351_502+1364d others(16): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr19 | 47719946 | ||||||
| chr19:47719946 | A | ATGTGTGT others(9): Show |
3 | a0001c0002t0003g0020 a0001c0002t0003g0030 a0001c0002t0003g0031 |
3 | HG02055.hp2 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.502+1349_502+1364d others(18): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr19 | 47719946 | ||||||
| chr19:47719946 | A | G | 25 | a0001c0001t0001g0309 a0001c0001t0001g0311 a0001c0001t0001g0313 others(22): Show |
26 | HG00639.hp1 HG00642.hp1 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.502+1340A>G | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | chr19 | 47719946 | |||||||
| chr19:47719946 | ATGTG | A | 18 | a0001c0001t0001g0337 a0001c0001t0001g0347 a0001c0001t0010g0300 others(15): Show |
19 | HG02145.hp1 HG02451.hp2 HG02486.hp1 others(16): Show |
intron_variant | MODIFIER | c.502+1361_502+1364d others(6): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr19 | 47719946 | ||||||
| chr19:47719983 | TC | T | 130 | a0001c0001t0001g0010 a0001c0001t0001g0024 a0001c0001t0001g0144 others(127): Show |
133 | HG00639.hp1 HG00642.hp1 HG00642.hp2 others(130): Show |
intron_variant | MODIFIER | c.502+1378delC | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | chr19 | 47719983 | |||||||
| chr19:47720113 | C | CTG | 6 | a0001c0002t0002g0200 a0001c0002t0002g0201 a0001c0002t0009g0150 others(3): Show |
6 | HG02074.hp2 HG02129.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.502+1526_502+1527d others(4): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr19 | 47720113 | ||||||
| chr19:47720113 | CTG | C | 46 | a0001c0001t0001g0024 a0001c0001t0001g0303 a0001c0002t0002g0036 others(43): Show |
48 | HG01074.hp2 HG01243.hp1 HG01243.hp2 others(45): Show |
intron_variant | MODIFIER | c.502+1526_502+1527d others(4): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr19 | 47720113 | ||||||
| chr19:47720225 | G | A | 1 | a0002c0009t0001g0035 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.502+1619G>A | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | chr19 | 47720225 | |||||||
| chr19:47720226 | C | T | 8 | a0001c0001t0001g0303 a0001c0002t0003g0070 a0001c0002t0006g0003 others(5): Show |
9 | HG01243.hp2 HG02258.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.502+1620C>T | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | chr19 | 47720226 | |||||||
| chr19:47720315 | C | T | 1 | a0001c0002t0003g0292 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.502+1709C>T | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | chr19 | 47720315 | |||||||
| chr19:47720328 | G | A | 1 | a0002c0007t0003g0032 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.502+1722G>A | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | chr19 | 47720328 | |||||||
| chr19:47720361 | G | T | 1 | a0002c0009t0001g0035 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.502+1755G>T | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | chr19 | 47720361 | |||||||
| chr19:47720551 | C | A | 1 | a0001c0004t0006g0272 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.502+1945C>A | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | chr19 | 47720551 | |||||||
| chr19:47720574 | C | CGT | 4 | a0001c0001t0001g0303 a0001c0002t0006g0003 a0001c0002t0006g0026 others(1): Show |
5 | HG01243.hp2 HG02258.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.502+1978_502+1979d others(4): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr19 | 47720574 | ||||||
| chr19:47720598 | A | C | 10 | a0001c0010t0005g0012 a0001c0010t0005g0015 a0001c0010t0005g0017 others(7): Show |
10 | HG01243.hp1 HG01255.hp1 HG01256.hp2 others(7): Show |
intron_variant | MODIFIER | c.502+1992A>C | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | chr19 | 47720598 | |||||||
| chr19:47720606 | C | A | 4 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0001g0389 others(1): Show |
4 | NA18954.hp1 NA18960.hp2 NA18961.hp1 others(1): Show |
intron_variant | MODIFIER | c.502+2000C>A | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | chr19 | 47720606 | |||||||
| chr19:47720660 | T | C | 1 | a0002c0009t0001g0035 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.502+2054T>C | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | chr19 | 47720660 | |||||||
| chr19:47720670 | T | C | 21 | a0001c0001t0001g0337 a0001c0001t0001g0347 a0001c0001t0010g0300 others(18): Show |
22 | HG02109.hp1 HG02145.hp1 HG02451.hp2 others(19): Show |
intron_variant | MODIFIER | c.502+2064T>C | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | chr19 | 47720670 | |||||||
| chr19:47721008 | A | C | 4 | a0001c0001t0001g0303 a0001c0002t0006g0003 a0001c0002t0006g0026 others(1): Show |
5 | HG01243.hp2 HG02258.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.502+2402A>C | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | chr19 | 47721008 | |||||||
| chr19:47721160 | TGG | T | 6 | a0001c0002t0002g0318 a0001c0002t0002g0319 a0001c0002t0003g0070 others(3): Show |
6 | HG02486.hp2 HG02630.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.502+2558_502+2559d others(4): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr19 | 47721160 | ||||||
| chr19:47721162 | GGGGT | G | 29 | a0001c0001t0001g0309 a0001c0001t0001g0311 a0001c0001t0001g0313 others(26): Show |
31 | HG00639.hp1 HG00642.hp1 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.502+2558_502+2561d others(6): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr19 | 47721162 | ||||||
| chr19:47721162 | GGGGTGT | G | 12 | a0001c0001t0001g0165 a0001c0001t0001g0303 a0001c0002t0006g0003 others(9): Show |
13 | HG01243.hp2 HG02109.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.502+2558_502+2563d others(8): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr19 | 47721162 | ||||||
| chr19:47721162 | GGGGTGTG others(1): Show |
G | 45 | a0001c0001t0001g0010 a0001c0001t0001g0144 a0001c0001t0001g0145 others(42): Show |
45 | HG00642.hp2 HG00738.hp2 HG01069.hp1 others(42): Show |
intron_variant | MODIFIER | c.502+2558_502+2565d others(10): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr19 | 47721162 | ||||||
| chr19:47721162 | GGGGTGTG others(3): Show |
G | 14 | a0001c0002t0003g0020 a0001c0002t0003g0030 a0001c0004t0003g0183 others(11): Show |
14 | HG01243.hp1 HG01255.hp1 HG01256.hp2 others(11): Show |
intron_variant | MODIFIER | c.502+2558_502+2567d others(12): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr19 | 47721162 | ||||||
| chr19:47721162 | GGGGTGTG others(7): Show |
G | 8 | a0001c0002t0002g0036 a0001c0002t0003g0004 a0001c0002t0003g0031 others(5): Show |
9 | HG01261.hp2 HG02055.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.502+2558_502+2571d others(16): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr19 | 47721162 | ||||||
| chr19:47721164 | G | GGT | 34 | a0001c0001t0001g0199 a0001c0001t0001g0255 a0001c0001t0001g0256 others(31): Show |
34 | HG00558.hp1 HG01884.hp1 HG01884.hp2 others(31): Show |
intron_variant | MODIFIER | c.502+2589_502+2590d others(4): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr19 | 47721164 | ||||||
| chr19:47721164 | G | T | 33 | a0001c0001t0001g0024 a0001c0001t0001g0337 a0001c0001t0001g0347 others(30): Show |
34 | HG01074.hp2 HG02145.hp1 HG02145.hp2 others(31): Show |
intron_variant | MODIFIER | c.502+2558G>T | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | chr19 | 47721164 | |||||||
| chr19:47721164 | GGT | G | 7 | a0001c0001t0001g0133 a0001c0001t0001g0267 a0001c0004t0002g0237 others(4): Show |
7 | HG00099.hp2 HG00673.hp1 HG00741.hp1 others(4): Show |
intron_variant | MODIFIER | c.502+2589_502+2590d others(4): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr19 | 47721164 | ||||||
| chr19:47721164 | GGTGT | G | 10 | a0001c0001t0001g0046 a0001c0001t0001g0061 a0001c0001t0001g0087 others(7): Show |
10 | HG01074.hp1 HG01081.hp1 HG01099.hp2 others(7): Show |
intron_variant | MODIFIER | c.502+2587_502+2590d others(6): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr19 | 47721164 | ||||||
| chr19:47721166 | T | G | 2 | a0001c0001t0001g0235 a0001c0018t0005g0086 |
2 | HG00280.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.502+2560T>G | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | chr19 | 47721166 | |||||||
| chr19:47721171 | GTGTGT | G | 32 | a0001c0001t0001g0024 a0001c0001t0001g0337 a0001c0001t0001g0347 others(29): Show |
33 | HG01074.hp2 HG02145.hp1 HG02145.hp2 others(30): Show |
intron_variant | MODIFIER | c.502+2566_502+2570d others(7): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | chr19 | 47721171 | |||||||
| chr19:47721200 | C | T | 4 | a0001c0001t0001g0259 a0001c0001t0001g0260 a0001c0001t0001g0261 others(1): Show |
4 | NA18948.hp1 NA18953.hp2 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.502+2594C>T | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | chr19 | 47721200 | |||||||
| chr19:47721247 | C | T | 1 | a0001c0003t0002g0008 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.502+2641C>T | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | chr19 | 47721247 | |||||||
| chr19:47721251 | T | C | 1 | a0002c0009t0001g0035 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.502+2645T>C | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | chr19 | 47721251 | |||||||
| chr19:47721324 | T | A | 39 | a0001c0001t0001g0024 a0001c0001t0001g0337 a0001c0001t0001g0347 others(36): Show |
41 | HG01074.hp2 HG01261.hp2 HG02145.hp1 others(38): Show |
intron_variant | MODIFIER | c.502+2718T>A | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | chr19 | 47721324 | |||||||
| chr19:47721565 | C | T | 1 | a0001c0001t0001g0224 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.502+2959C>T | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | chr19 | 47721565 | |||||||
| chr19:47721576 | AG | A | 3 | a0001c0001t0001g0024 a0001c0002t0003g0292 a0001c0015t0001g0302 |
3 | HG01074.hp2 HG02615.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.502+2971delG | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | chr19 | 47721576 | |||||||
| chr19:47721705 | C | T | 1 | a0001c0004t0006g0272 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.502+3099C>T | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | chr19 | 47721705 | |||||||
| chr19:47721920 | G | A | 82 | a0001c0001t0001g0010 a0001c0001t0001g0144 a0001c0001t0001g0145 others(79): Show |
84 | HG00639.hp1 HG00642.hp1 HG00642.hp2 others(81): Show |
intron_variant | MODIFIER | c.502+3314G>A | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | chr19 | 47721920 | |||||||
| chr19:47721964 | G | A | 1 | a0001c0003t0002g0362 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.502+3358G>A | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | chr19 | 47721964 | |||||||
| chr19:47722009 | A | AAC | 36 | a0001c0001t0001g0073 a0001c0001t0001g0080 a0001c0001t0001g0084 others(33): Show |
36 | HG00099.hp1 HG00558.hp1 HG00621.hp1 others(33): Show |
intron_variant | MODIFIER | c.502+3450_502+3451d others(4): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr19 | 47722009 | ||||||
| chr19:47722009 | A | AACAC | 4 | a0001c0001t0001g0076 a0001c0001t0018g0044 a0001c0002t0002g0143 others(1): Show |
4 | HG03491.hp1 HG03669.hp1 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.502+3448_502+3451d others(6): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr19 | 47722009 | ||||||
| chr19:47722009 | AAC | A | 49 | a0001c0001t0001g0055 a0001c0001t0001g0056 a0001c0001t0001g0057 others(46): Show |
50 | HG00323.hp2 HG00438.hp2 HG00544.hp1 others(47): Show |
intron_variant | MODIFIER | c.502+3450_502+3451d others(4): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr19 | 47722009 | ||||||
| chr19:47722009 | AACAC | A | 31 | a0001c0001t0001g0010 a0001c0001t0001g0024 a0001c0001t0001g0058 others(28): Show |
32 | HG00140.hp1 HG00280.hp1 HG01256.hp1 others(29): Show |
intron_variant | MODIFIER | c.502+3448_502+3451d others(6): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr19 | 47722009 | ||||||
| chr19:47722009 | AACACAC | A | 13 | a0001c0001t0001g0199 a0001c0001t0001g0347 a0001c0001t0001g0369 others(10): Show |
13 | HG01261.hp2 HG02055.hp2 HG02523.hp1 others(10): Show |
intron_variant | MODIFIER | c.502+3446_502+3451d others(8): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr19 | 47722009 | ||||||
| chr19:47722009 | AACACACA others(1): Show |
A | 49 | a0001c0001t0001g0028 a0001c0001t0001g0061 a0001c0001t0001g0062 others(46): Show |
49 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(46): Show |
intron_variant | MODIFIER | c.502+3444_502+3451d others(10): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr19 | 47722009 | ||||||
| chr19:47722009 | AACACACA others(3): Show |
A | 6 | a0001c0001t0001g0019 a0001c0002t0002g0025 a0001c0010t0005g0012 others(3): Show |
6 | HG00280.hp2 HG01255.hp1 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.502+3442_502+3451d others(12): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr19 | 47722009 | ||||||
| chr19:47722009 | AACACACA others(5): Show |
A | 13 | a0001c0001t0001g0303 a0001c0002t0003g0292 a0001c0002t0006g0003 others(10): Show |
14 | HG01074.hp2 HG01243.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.502+3440_502+3451d others(14): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr19 | 47722009 | ||||||
| chr19:47722009 | AACACACA others(7): Show |
A | 6 | a0001c0002t0002g0001 a0001c0002t0006g0304 a0001c0003t0002g0139 others(3): Show |
7 | HG01243.hp1 HG02683.hp2 HG03579.hp1 others(4): Show |
intron_variant | MODIFIER | c.502+3438_502+3451d others(16): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr19 | 47722009 | ||||||
| chr19:47722009 | AACACACA others(9): Show |
A | 1 | a0002c0007t0006g0037 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.502+3436_502+3451d others(18): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr19 | 47722009 | ||||||
| chr19:47722057 | C | CACACAG | 7 | a0001c0001t0001g0173 a0001c0002t0002g0216 a0001c0002t0002g0217 others(4): Show |
8 | HG01516.hp1 HG01517.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.502+3451_502+3452i others(8): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | chr19 | 47722057 | |||||||
| chr19:47722057 | C | CACAG | 9 | a0001c0001t0001g0309 a0001c0002t0002g0174 a0001c0002t0002g0319 others(6): Show |
9 | HG01993.hp1 HG02165.hp1 HG02293.hp2 others(6): Show |
intron_variant | MODIFIER | c.502+3451_502+3452i others(6): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | chr19 | 47722057 | |||||||
| chr19:47722057 | C | CAG | 35 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0165 others(32): Show |
36 | HG00639.hp1 HG00642.hp1 HG00735.hp2 others(33): Show |
intron_variant | MODIFIER | c.502+3451_502+3452i others(4): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | chr19 | 47722057 | |||||||
| chr19:47722057 | C | G | 95 | a0001c0001t0001g0010 a0001c0001t0001g0024 a0001c0001t0001g0169 others(92): Show |
98 | HG00642.hp2 HG00738.hp1 HG00738.hp2 others(95): Show |
intron_variant | MODIFIER | c.502+3451C>G | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | chr19 | 47722057 | |||||||
| chr19:47722108 | T | C | 1 | a0001c0001t0001g0384 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.502+3502T>C | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | chr19 | 47722108 | |||||||
| chr19:47722311 | G | A | 1 | a0001c0001t0001g0103 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.503-3501G>A | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | chr19 | 47722311 | |||||||
| chr19:47722348 | G | C | 3 | a0001c0008t0005g0363 a0001c0008t0005g0364 a0001c0008t0005g0365 |
3 | HG00099.hp2 HG00741.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.503-3464G>C | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | chr19 | 47722348 | |||||||
| chr19:47722382 | C | T | 1 | a0001c0001t0001g0277 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.503-3430C>T | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | chr19 | 47722382 | |||||||
| chr19:47722436 | C | T | 3 | a0001c0002t0004g0297 a0001c0002t0004g0299 a0001c0002t0017g0298 |
3 | HG01884.hp2 HG03225.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.503-3376C>T | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | chr19 | 47722436 | |||||||
| chr19:47722437 | G | A | 5 | a0001c0004t0003g0021 a0001c0004t0003g0022 a0001c0004t0019g0023 others(2): Show |
5 | HG02109.hp2 HG02559.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.503-3375G>A | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | chr19 | 47722437 | |||||||
| chr19:47722470 | T | C | 102 | a0001c0001t0001g0010 a0001c0001t0001g0144 a0001c0001t0001g0145 others(99): Show |
103 | HG00639.hp1 HG00642.hp1 HG00642.hp2 others(100): Show |
intron_variant | MODIFIER | c.503-3342T>C | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | chr19 | 47722470 | |||||||
| chr19:47722569 | C | CT | 88 | a0001c0001t0001g0010 a0001c0001t0001g0144 a0001c0001t0001g0145 others(85): Show |
89 | HG00639.hp1 HG00642.hp1 HG00642.hp2 others(86): Show |
intron_variant | MODIFIER | c.503-3230dupT | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr19 | 47722569 | ||||||
| chr19:47722569 | C | CTT | 13 | a0001c0002t0002g0036 a0001c0002t0002g0305 a0001c0002t0004g0281 others(10): Show |
13 | HG01243.hp1 HG01255.hp1 HG01256.hp2 others(10): Show |
intron_variant | MODIFIER | c.503-3231_503-3230d others(4): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr19 | 47722569 | ||||||
| chr19:47722569 | CT | C | 7 | a0001c0001t0001g0028 a0001c0001t0001g0153 a0001c0001t0001g0202 others(4): Show |
7 | HG00323.hp2 HG01516.hp2 NA18948.hp1 others(4): Show |
intron_variant | MODIFIER | c.503-3230delT | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr19 | 47722569 | ||||||
| chr19:47722691 | G | A | 4 | a0001c0001t0010g0300 a0001c0001t0010g0344 a0001c0001t0010g0350 others(1): Show |
4 | HG02145.hp1 HG03195.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.503-3121G>A | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | chr19 | 47722691 | |||||||
| chr19:47722732 | A | T | 2 | a0001c0002t0002g0036 a0001c0002t0004g0281 |
2 | HG01261.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.503-3080A>T | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | chr19 | 47722732 | |||||||
| chr19:47722779 | G | A | 3 | a0001c0001t0001g0024 a0001c0002t0003g0292 a0001c0015t0001g0302 |
3 | HG01074.hp2 HG02615.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.503-3033G>A | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | chr19 | 47722779 | |||||||
| chr19:47722839 | A | G | 161 | a0001c0001t0001g0010 a0001c0001t0001g0078 a0001c0001t0001g0100 others(158): Show |
163 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(160): Show |
intron_variant | MODIFIER | c.503-2973A>G | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | chr19 | 47722839 | |||||||
| chr19:47723141 | C | T | 143 | a0001c0001t0001g0010 a0001c0001t0001g0144 a0001c0001t0001g0145 others(140): Show |
145 | HG00099.hp1 HG00558.hp2 HG00642.hp1 others(142): Show |
intron_variant | MODIFIER | c.503-2671C>T | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | chr19 | 47723141 | |||||||
| chr19:47723325 | A | T | 157 | a0001c0001t0001g0010 a0001c0001t0001g0080 a0001c0001t0001g0129 others(154): Show |
159 | HG00099.hp1 HG00558.hp2 HG00621.hp1 others(156): Show |
intron_variant | MODIFIER | c.503-2487A>T | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | chr19 | 47723325 | |||||||
| chr19:47723331 | A | G | 1 | a0002c0009t0001g0035 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.503-2481A>G | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | chr19 | 47723331 | |||||||
| chr19:47723352 | G | A | 3 | a0001c0001t0010g0300 a0001c0001t0010g0344 a0001c0001t0010g0350 |
3 | HG03195.hp2 HG03209.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.503-2460G>A | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | chr19 | 47723352 | |||||||
| chr19:47723383 | C | T | 15 | a0001c0001t0001g0303 a0001c0002t0003g0004 a0001c0002t0003g0020 others(12): Show |
17 | HG02055.hp2 HG02258.hp2 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.503-2429C>T | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | chr19 | 47723383 | |||||||
| chr19:47723561 | C | G | 61 | a0001c0001t0001g0235 a0001c0001t0001g0242 a0001c0001t0001g0270 others(58): Show |
62 | HG00558.hp2 HG01256.hp1 HG01361.hp1 others(59): Show |
intron_variant | MODIFIER | c.503-2251C>G | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | chr19 | 47723561 | |||||||
| chr19:47723648 | C | T | 1 | a0001c0001t0001g0347 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.503-2164C>T | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | chr19 | 47723648 | |||||||
| chr19:47723653 | G | GA | 146 | a0001c0001t0001g0010 a0001c0001t0001g0055 a0001c0001t0001g0066 others(143): Show |
149 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(146): Show |
intron_variant | MODIFIER | c.503-2139dupA | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr19 | 47723653 | ||||||
| chr19:47723653 | G | GAA | 52 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0177 others(49): Show |
52 | HG00621.hp2 HG00642.hp1 HG00642.hp2 others(49): Show |
intron_variant | MODIFIER | c.503-2140_503-2139d others(4): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr19 | 47723653 | ||||||
| chr19:47723653 | GA | G | 11 | a0001c0001t0001g0119 a0001c0001t0001g0208 a0001c0001t0001g0347 others(8): Show |
11 | HG01167.hp2 HG02145.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.503-2139delA | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr19 | 47723653 | ||||||
| chr19:47723653 | GAA | G | 7 | a0001c0002t0003g0027 a0001c0002t0003g0225 a0001c0002t0003g0288 others(4): Show |
8 | HG02056.hp2 HG02615.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.503-2140_503-2139d others(4): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr19 | 47723653 | ||||||
| chr19:47723675 | C | T | 11 | a0001c0001t0001g0337 a0001c0002t0002g0171 a0001c0002t0002g0319 others(8): Show |
12 | HG02572.hp2 HG02615.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.503-2137C>T | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | chr19 | 47723675 | |||||||
| chr19:47723682 | AT | A | 49 | a0001c0001t0001g0232 a0001c0001t0001g0235 a0001c0001t0001g0337 others(46): Show |
50 | HG00099.hp2 HG00741.hp1 HG01074.hp2 others(47): Show |
intron_variant | MODIFIER | c.503-2119delT | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr19 | 47723682 | ||||||
| chr19:47723685 | T | G | 11 | a0001c0001t0001g0337 a0001c0002t0002g0171 a0001c0002t0002g0319 others(8): Show |
12 | HG02572.hp2 HG02615.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.503-2127T>G | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | chr19 | 47723685 | |||||||
| chr19:47723813 | G | C | 16 | a0001c0001t0001g0303 a0001c0002t0003g0004 a0001c0002t0003g0020 others(13): Show |
18 | HG02055.hp2 HG02258.hp2 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.503-1999G>C | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | chr19 | 47723813 | |||||||
| chr19:47724076 | C | T | 1 | a0001c0001t0001g0267 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.503-1736C>T | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | chr19 | 47724076 | |||||||
| chr19:47724083 | C | CT | 130 | a0001c0001t0001g0010 a0001c0001t0001g0144 a0001c0001t0001g0173 others(127): Show |
132 | HG00099.hp1 HG00642.hp1 HG00642.hp2 others(129): Show |
intron_variant | MODIFIER | c.503-1716dupT | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr19 | 47724083 | ||||||
| chr19:47724083 | CT | C | 12 | a0001c0001t0001g0076 a0001c0004t0003g0021 a0001c0004t0003g0022 others(9): Show |
12 | HG02109.hp2 HG02145.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.503-1716delT | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr19 | 47724083 | ||||||
| chr19:47724179 | A | G | 14 | a0001c0002t0003g0004 a0001c0002t0003g0020 a0001c0002t0003g0030 others(11): Show |
16 | HG02055.hp2 HG02451.hp2 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.503-1633A>G | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | chr19 | 47724179 | |||||||
| chr19:47724260 | T | A | 1 | a0005c0017t0014g0206 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.503-1552T>A | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | chr19 | 47724260 | |||||||
| chr19:47724312 | G | C | 43 | a0001c0001t0001g0337 a0001c0001t0010g0300 a0001c0001t0010g0344 others(40): Show |
44 | HG00099.hp2 HG00741.hp1 HG01074.hp2 others(41): Show |
intron_variant | MODIFIER | c.503-1500G>C | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | chr19 | 47724312 | |||||||
| chr19:47724442 | T | C | 44 | a0001c0001t0001g0337 a0001c0001t0010g0300 a0001c0001t0010g0344 others(41): Show |
45 | HG00099.hp2 HG00741.hp1 HG01074.hp2 others(42): Show |
intron_variant | MODIFIER | c.503-1370T>C | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | chr19 | 47724442 | |||||||
| chr19:47724467 | A | C | 44 | a0001c0001t0001g0337 a0001c0001t0010g0300 a0001c0001t0010g0344 others(41): Show |
45 | HG00099.hp2 HG00741.hp1 HG01074.hp2 others(42): Show |
intron_variant | MODIFIER | c.503-1345A>C | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | chr19 | 47724467 | |||||||
| chr19:47724695 | G | A | 1 | a0001c0001t0001g0088 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.503-1117G>A | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | chr19 | 47724695 | |||||||
| chr19:47724752 | C | T | 1 | a0001c0003t0002g0310 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.503-1060C>T | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | chr19 | 47724752 | |||||||
| chr19:47724776 | T | A | 43 | a0001c0001t0001g0337 a0001c0001t0010g0300 a0001c0001t0010g0344 others(40): Show |
44 | HG00099.hp2 HG00741.hp1 HG01074.hp2 others(41): Show |
intron_variant | MODIFIER | c.503-1036T>A | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | chr19 | 47724776 | |||||||
| chr19:47724814 | T | G | 1 | a0001c0002t0003g0294 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.503-998T>G | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | chr19 | 47724814 | |||||||
| chr19:47724869 | G | A | 1 | a0001c0002t0002g0047 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.503-943G>A | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | chr19 | 47724869 | |||||||
| chr19:47724947 | A | T | 1 | a0001c0001t0001g0356 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.503-865A>T | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | chr19 | 47724947 | |||||||
| chr19:47724981 | CAAA | C | 17 | a0001c0001t0001g0078 a0001c0001t0001g0083 a0001c0001t0001g0121 others(14): Show |
17 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(14): Show |
intron_variant | MODIFIER | c.503-795_503-793del others(3): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr19 | 47724981 | ||||||
| chr19:47724981 | CAAAA | C | 49 | a0001c0001t0001g0056 a0001c0001t0001g0062 a0001c0001t0001g0074 others(46): Show |
49 | HG00280.hp1 HG00438.hp2 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.503-796_503-793del others(4): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr19 | 47724981 | ||||||
| chr19:47724981 | CAAAAA | C | 50 | a0001c0001t0001g0046 a0001c0001t0001g0055 a0001c0001t0001g0057 others(47): Show |
50 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(47): Show |
intron_variant | MODIFIER | c.503-797_503-793del others(5): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr19 | 47724981 | ||||||
| chr19:47724981 | CAAAAAA | C | 20 | a0001c0001t0001g0050 a0001c0001t0001g0081 a0001c0001t0001g0116 others(17): Show |
20 | HG00738.hp2 HG01192.hp2 HG01255.hp2 others(17): Show |
intron_variant | MODIFIER | c.503-798_503-793del others(6): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr19 | 47724981 | ||||||
| chr19:47724981 | CAAAAAAA | C | 24 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0024 others(21): Show |
24 | HG00280.hp2 HG00544.hp1 HG00544.hp2 others(21): Show |
intron_variant | MODIFIER | c.503-799_503-793del others(7): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr19 | 47724981 | ||||||
| chr19:47724981 | CAAAAAAA others(1): Show |
C | 72 | a0001c0001t0001g0028 a0001c0001t0001g0058 a0001c0001t0001g0068 others(69): Show |
73 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(70): Show |
intron_variant | MODIFIER | c.503-800_503-793del others(8): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr19 | 47724981 | ||||||
| chr19:47724981 | CAAAAAAA others(2): Show |
C | 79 | a0001c0001t0001g0235 a0001c0001t0001g0303 a0001c0001t0001g0347 others(76): Show |
82 | HG00558.hp2 HG00642.hp1 HG00738.hp1 others(79): Show |
intron_variant | MODIFIER | c.503-801_503-793del others(9): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr19 | 47724981 | ||||||
| chr19:47724981 | CAAAAAAA others(3): Show |
C | 21 | a0001c0001t0001g0313 a0001c0001t0001g0314 a0001c0001t0001g0328 others(18): Show |
22 | HG00099.hp1 HG00735.hp2 HG01168.hp2 others(19): Show |
intron_variant | MODIFIER | c.503-802_503-793del others(10): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr19 | 47724981 | ||||||
| chr19:47724981 | CAAAAAAA others(4): Show |
C | 2 | a0001c0002t0002g0009 a0001c0003t0002g0316 |
2 | HG01070.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.503-803_503-793del others(11): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr19 | 47724981 | ||||||
| chr19:47724981 | CAAAAAAA others(8): Show |
C | 11 | a0001c0008t0005g0341 a0001c0008t0005g0363 a0001c0008t0005g0364 others(8): Show |
11 | HG00099.hp2 HG00741.hp1 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.503-807_503-793del others(15): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr19 | 47724981 | ||||||
| chr19:47724981 | CAAAAAAA others(9): Show |
C | 13 | a0001c0001t0001g0337 a0001c0002t0002g0171 a0001c0002t0002g0319 others(10): Show |
14 | HG02572.hp2 HG02615.hp1 HG02717.hp1 others(11): Show |
intron_variant | MODIFIER | c.503-808_503-793del others(16): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr19 | 47724981 | ||||||
| chr19:47724981 | CAAAAAAA others(10): Show |
C | 12 | a0001c0003t0002g0310 a0001c0004t0003g0021 a0001c0004t0003g0022 others(9): Show |
12 | HG01891.hp2 HG02109.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.503-809_503-793del others(17): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr19 | 47724981 | ||||||
| chr19:47724981 | CAAAAAAA others(11): Show |
C | 4 | a0001c0001t0010g0300 a0001c0001t0010g0344 a0001c0001t0010g0350 others(1): Show |
4 | HG02165.hp1 HG03195.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.503-810_503-793del others(18): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr19 | 47724981 | ||||||
| chr19:47724981 | CAAAAAAA others(13): Show |
C | 1 | a0001c0024t0001g0329 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.503-812_503-793del others(20): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr19 | 47724981 | ||||||
| chr19:47724981 | CAAAAAAA others(14): Show |
C | 4 | a0001c0004t0002g0043 a0001c0004t0002g0237 a0001c0015t0001g0104 others(1): Show |
4 | HG01074.hp2 HG02040.hp2 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.503-813_503-793del others(21): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr19 | 47724981 | ||||||
| chr19:47725080 | G | A | 1 | a0001c0024t0001g0329 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.503-732G>A | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | chr19 | 47725080 | |||||||
| chr19:47725199 | T | C | 29 | a0001c0004t0002g0043 a0001c0004t0002g0237 a0001c0004t0003g0021 others(26): Show |
29 | HG00099.hp2 HG00741.hp1 HG01074.hp2 others(26): Show |
intron_variant | MODIFIER | c.503-613T>C | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | chr19 | 47725199 | |||||||
| chr19:47725206 | A | C | 13 | a0001c0001t0001g0337 a0001c0002t0002g0171 a0001c0002t0002g0319 others(10): Show |
14 | HG02280.hp2 HG02572.hp2 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.503-606A>C | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | chr19 | 47725206 | |||||||
| chr19:47725358 | C | T | 140 | a0001c0001t0001g0010 a0001c0001t0001g0144 a0001c0001t0001g0145 others(137): Show |
143 | HG00099.hp1 HG00558.hp2 HG00642.hp1 others(140): Show |
intron_variant | MODIFIER | c.503-454C>T | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | chr19 | 47725358 | |||||||
| chr19:47725396 | C | CA | 48 | a0001c0001t0001g0056 a0001c0001t0001g0061 a0001c0001t0001g0083 others(45): Show |
49 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(46): Show |
intron_variant | MODIFIER | c.503-393dupA | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr19 | 47725396 | ||||||
| chr19:47725396 | C | CAA | 98 | a0001c0001t0001g0111 a0001c0001t0001g0144 a0001c0001t0001g0145 others(95): Show |
100 | HG00099.hp1 HG00558.hp2 HG00735.hp2 others(97): Show |
intron_variant | MODIFIER | c.503-394_503-393dup others(2): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr19 | 47725396 | ||||||
| chr19:47725396 | C | CAAA | 26 | a0001c0001t0001g0235 a0001c0002t0002g0174 a0001c0002t0002g0201 others(23): Show |
26 | HG00642.hp1 HG00642.hp2 HG01175.hp2 others(23): Show |
intron_variant | MODIFIER | c.503-395_503-393dup others(3): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr19 | 47725396 | ||||||
| chr19:47725396 | C | CAAAA | 21 | a0001c0001t0001g0010 a0001c0002t0002g0217 a0001c0002t0002g0367 others(18): Show |
23 | HG00738.hp1 HG01106.hp2 HG02451.hp2 others(20): Show |
intron_variant | MODIFIER | c.503-396_503-393dup others(4): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr19 | 47725396 | ||||||
| chr19:47725396 | C | CAAAAA | 6 | a0001c0002t0002g0216 a0001c0002t0003g0030 a0001c0002t0003g0031 others(3): Show |
6 | HG02055.hp2 HG03195.hp1 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.503-397_503-393dup others(5): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr19 | 47725396 | ||||||
| chr19:47725396 | C | CAAAAAAA others(2): Show |
10 | a0001c0001t0001g0337 a0001c0002t0002g0171 a0001c0002t0002g0319 others(7): Show |
11 | HG02572.hp2 HG02615.hp1 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.503-401_503-393dup others(9): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr19 | 47725396 | ||||||
| chr19:47725396 | C | CAAAAAAA others(4): Show |
1 | a0001c0002t0003g0225 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.503-403_503-393dup others(11): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr19 | 47725396 | ||||||
| chr19:47725396 | CA | C | 24 | a0001c0001t0001g0046 a0001c0001t0001g0115 a0001c0001t0001g0151 others(21): Show |
24 | HG00741.hp1 HG01069.hp2 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.503-393delA | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr19 | 47725396 | ||||||
| chr19:47725437 | T | C | 177 | a0001c0001t0001g0010 a0001c0001t0001g0144 a0001c0001t0001g0145 others(174): Show |
180 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(177): Show |
intron_variant | MODIFIER | c.503-375T>C | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | chr19 | 47725437 | |||||||
| chr19:47725559 | G | A | 1 | a0001c0003t0002g0139 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.503-253G>A | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | chr19 | 47725559 | |||||||
| chr19:47725589 | G | C | 5 | a0001c0004t0003g0021 a0001c0004t0003g0022 a0001c0004t0019g0023 others(2): Show |
5 | HG02109.hp2 HG02145.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.503-223G>C | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | chr19 | 47725589 | |||||||
| chr19:47725632 | C | A | 20 | a0001c0001t0001g0337 a0001c0002t0002g0171 a0001c0002t0002g0319 others(17): Show |
21 | HG01891.hp1 HG02055.hp1 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.503-180C>A | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 3/5 | chr19 | 47725632 | |||||||
| chr19:47726252 | A | G | 1 | a0001c0001t0001g0057 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.915+28A>G | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47726252 | |||||||
| chr19:47726256 | T | C | 5 | a0001c0002t0002g0036 a0002c0007t0007g0290 a0002c0007t0007g0291 others(2): Show |
5 | HG01261.hp2 HG02145.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.915+32T>C | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47726256 | |||||||
| chr19:47726274 | G | A | 7 | a0001c0002t0006g0003 a0001c0002t0006g0026 a0001c0002t0006g0033 others(4): Show |
8 | HG01243.hp2 HG02257.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.915+50G>A | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47726274 | |||||||
| chr19:47726430 | G | A | 2 | a0001c0001t0001g0083 a0001c0018t0005g0086 |
2 | HG00140.hp1 HG00280.hp1 |
intron_variant | MODIFIER | c.915+206G>A | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47726430 | |||||||
| chr19:47726452 | G | A | 1 | a0001c0001t0001g0313 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.915+228G>A | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47726452 | |||||||
| chr19:47726475 | TTCC | T | 59 | a0001c0001t0001g0235 a0001c0002t0002g0001 a0001c0002t0002g0040 others(56): Show |
60 | HG00558.hp2 HG01256.hp1 HG01361.hp1 others(57): Show |
intron_variant | MODIFIER | c.915+265_915+267del others(3): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 47726475 | ||||||
| chr19:47726544 | CTCT | C | 127 | a0001c0001t0001g0010 a0001c0001t0001g0144 a0001c0001t0001g0145 others(124): Show |
129 | HG00099.hp1 HG00558.hp2 HG00642.hp1 others(126): Show |
intron_variant | MODIFIER | c.915+327_915+329del others(3): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 47726544 | ||||||
| chr19:47726554 | CCCT | C | 17 | a0001c0002t0004g0059 a0001c0002t0004g0297 a0001c0002t0004g0299 others(14): Show |
17 | HG00099.hp2 HG00741.hp1 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.915+343_915+345del others(3): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 47726554 | ||||||
| chr19:47726569 | T | G | 6 | a0001c0002t0004g0059 a0001c0002t0004g0297 a0001c0002t0004g0299 others(3): Show |
6 | HG01884.hp1 HG01884.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.915+345T>G | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47726569 | |||||||
| chr19:47726589 | C | T | 7 | a0001c0002t0006g0003 a0001c0002t0006g0026 a0001c0002t0006g0033 others(4): Show |
8 | HG01243.hp2 HG02257.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.915+365C>T | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47726589 | |||||||
| chr19:47726668 | C | T | 1 | a0001c0003t0002g0315 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.915+444C>T | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47726668 | |||||||
| chr19:47726824 | A | G | 385 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0024 others(382): Show |
391 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(388): Show |
intron_variant | MODIFIER | c.915+600A>G | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47726824 | |||||||
| chr19:47726835 | C | A | 3 | a0001c0001t0010g0300 a0001c0001t0010g0344 a0001c0001t0010g0350 |
3 | HG03195.hp2 HG03209.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.915+611C>A | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47726835 | |||||||
| chr19:47727113 | T | C | 8 | a0001c0001t0001g0337 a0001c0002t0003g0027 a0001c0002t0003g0225 others(5): Show |
9 | HG02615.hp1 HG02717.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.915+889T>C | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47727113 | |||||||
| chr19:47727115 | T | C | 3 | a0001c0001t0010g0300 a0001c0001t0010g0344 a0001c0001t0010g0350 |
3 | HG03195.hp2 HG03209.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.915+891T>C | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47727115 | |||||||
| chr19:47727121 | T | C | 5 | a0001c0002t0002g0036 a0002c0007t0007g0290 a0002c0007t0007g0291 others(2): Show |
5 | HG01261.hp2 HG02145.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.915+897T>C | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47727121 | |||||||
| chr19:47727173 | C | T | 7 | a0001c0002t0006g0003 a0001c0002t0006g0026 a0001c0002t0006g0033 others(4): Show |
8 | HG01243.hp2 HG02257.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.915+949C>T | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47727173 | |||||||
| chr19:47727174 | G | C | 1 | a0001c0002t0002g0198 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.915+950G>C | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47727174 | |||||||
| chr19:47727265 | C | T | 3 | a0001c0002t0004g0147 a0001c0002t0004g0148 a0001c0002t0004g0149 |
3 | HG01891.hp1 HG02055.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.915+1041C>T | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47727265 | |||||||
| chr19:47727303 | G | A | 21 | a0001c0001t0001g0303 a0001c0002t0002g0036 a0001c0002t0003g0004 others(18): Show |
23 | HG01261.hp2 HG02055.hp2 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.915+1079G>A | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47727303 | |||||||
| chr19:47727340 | G | T | 6 | a0001c0004t0002g0043 a0001c0004t0002g0237 a0001c0015t0001g0104 others(3): Show |
6 | HG01074.hp2 HG02040.hp2 HG02056.hp2 others(3): Show |
intron_variant | MODIFIER | c.915+1116G>T | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47727340 | |||||||
| chr19:47727471 | C | T | 19 | a0001c0001t0001g0083 a0001c0004t0002g0043 a0001c0004t0002g0237 others(16): Show |
19 | HG00140.hp1 HG01074.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.915+1247C>T | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47727471 | |||||||
| chr19:47727494 | T | A | 1 | a0001c0002t0003g0348 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.915+1270T>A | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47727494 | |||||||
| chr19:47727548 | G | GGGAGTTG others(10): Show |
1 | a0001c0002t0008g0286 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.915+1325_915+1341d others(19): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 47727548 | ||||||
| chr19:47727582 | G | A | 12 | a0001c0002t0002g0171 a0001c0002t0002g0319 a0001c0002t0004g0038 others(9): Show |
12 | HG01891.hp1 HG02055.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.915+1358G>A | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47727582 | |||||||
| chr19:47727702 | TA | T | 11 | a0001c0001t0001g0117 a0001c0001t0001g0232 a0001c0001t0001g0303 others(8): Show |
11 | HG01168.hp2 HG01256.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.915+1494delA | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 47727702 | ||||||
| chr19:47727751 | C | T | 6 | a0001c0005t0002g0156 a0001c0005t0002g0157 a0001c0005t0002g0187 others(3): Show |
6 | NA18612.hp2 NA18947.hp1 NA18961.hp2 others(3): Show |
intron_variant | MODIFIER | c.915+1527C>T | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47727751 | |||||||
| chr19:47727752 | G | A | 3 | a0001c0004t0002g0043 a0001c0015t0001g0104 a0001c0015t0001g0302 |
3 | HG01074.hp2 HG02040.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.915+1528G>A | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47727752 | |||||||
| chr19:47727964 | C | T | 16 | a0001c0001t0001g0303 a0001c0002t0003g0004 a0001c0002t0003g0020 others(13): Show |
18 | HG02055.hp2 HG02258.hp2 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.915+1740C>T | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47727964 | |||||||
| chr19:47728074 | C | T | 187 | a0001c0001t0001g0010 a0001c0001t0001g0144 a0001c0001t0001g0145 others(184): Show |
193 | HG00099.hp1 HG00558.hp2 HG00642.hp1 others(190): Show |
intron_variant | MODIFIER | c.915+1850C>T | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47728074 | |||||||
| chr19:47728082 | C | T | 1 | a0003c0006t0001g0155 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.915+1858C>T | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47728082 | |||||||
| chr19:47728095 | C | CA | 31 | a0001c0001t0001g0303 a0001c0002t0002g0007 a0001c0002t0002g0036 others(28): Show |
34 | HG01243.hp2 HG01261.hp2 HG01884.hp1 others(31): Show |
intron_variant | MODIFIER | c.915+1875dupA | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 47728095 | ||||||
| chr19:47728095 | C | CAA | 120 | a0001c0001t0001g0010 a0001c0001t0001g0144 a0001c0001t0001g0145 others(117): Show |
122 | HG00099.hp1 HG00558.hp2 HG00642.hp1 others(119): Show |
intron_variant | MODIFIER | c.915+1874_915+1875d others(4): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 47728095 | ||||||
| chr19:47728095 | C | CAAA | 7 | a0001c0002t0002g0250 a0001c0002t0002g0273 a0001c0003t0002g0315 others(4): Show |
7 | HG01070.hp2 HG02135.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.915+1873_915+1875d others(5): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 47728095 | ||||||
| chr19:47728100 | T | A | 163 | a0001c0001t0001g0010 a0001c0001t0001g0144 a0001c0001t0001g0145 others(160): Show |
168 | HG00099.hp1 HG00558.hp2 HG00642.hp1 others(165): Show |
intron_variant | MODIFIER | c.915+1876T>A | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47728100 | |||||||
| chr19:47728100 | T | TA | 17 | a0001c0001t0010g0300 a0001c0001t0010g0344 a0001c0001t0010g0350 others(14): Show |
17 | HG01891.hp1 HG02055.hp1 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.915+1891dupA | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 47728100 | ||||||
| chr19:47728100 | T | TAA | 7 | a0001c0001t0001g0337 a0001c0002t0003g0027 a0001c0002t0003g0225 others(4): Show |
8 | HG02615.hp1 HG02622.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.915+1890_915+1891d others(4): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 47728100 | ||||||
| chr19:47728100 | TA | T | 13 | a0001c0001t0001g0073 a0001c0001t0001g0196 a0001c0002t0002g0170 others(10): Show |
13 | HG00099.hp2 HG00741.hp1 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.915+1891delA | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 47728100 | ||||||
| chr19:47728243 | G | A | 1 | a0001c0002t0002g0305 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.915+2019G>A | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47728243 | |||||||
| chr19:47728316 | C | T | 173 | a0001c0001t0001g0010 a0001c0001t0001g0144 a0001c0001t0001g0145 others(170): Show |
178 | HG00099.hp1 HG00558.hp2 HG00642.hp1 others(175): Show |
intron_variant | MODIFIER | c.915+2092C>T | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47728316 | |||||||
| chr19:47728359 | C | T | 11 | a0001c0008t0005g0341 a0001c0008t0005g0363 a0001c0008t0005g0364 others(8): Show |
11 | HG00099.hp2 HG00741.hp1 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.915+2135C>T | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47728359 | |||||||
| chr19:47728391 | C | T | 170 | a0001c0001t0001g0010 a0001c0001t0001g0144 a0001c0001t0001g0145 others(167): Show |
175 | HG00099.hp1 HG00558.hp2 HG00642.hp1 others(172): Show |
intron_variant | MODIFIER | c.915+2167C>T | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47728391 | |||||||
| chr19:47728523 | G | A | 3 | a0001c0001t0001g0117 a0001c0001t0001g0215 a0001c0019t0001g0134 |
3 | HG02738.hp1 HG03017.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.915+2299G>A | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47728523 | |||||||
| chr19:47728571 | C | CT | 45 | a0001c0001t0001g0199 a0001c0001t0001g0271 a0001c0001t0001g0303 others(42): Show |
48 | HG00099.hp1 HG00642.hp1 HG01168.hp2 others(45): Show |
intron_variant | MODIFIER | c.915+2362dupT | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 47728571 | ||||||
| chr19:47728571 | CT | C | 9 | a0001c0001t0001g0153 a0001c0001t0001g0177 a0001c0002t0002g0204 others(6): Show |
9 | HG00323.hp2 HG00738.hp2 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.915+2362delT | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 47728571 | ||||||
| chr19:47728575 | T | C | 11 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0337 others(8): Show |
12 | HG01074.hp1 HG01099.hp2 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.915+2351T>C | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47728575 | |||||||
| chr19:47728592 | A | G | 3 | a0001c0001t0010g0300 a0001c0001t0010g0344 a0001c0001t0010g0350 |
3 | HG03195.hp2 HG03209.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.915+2368A>G | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47728592 | |||||||
| chr19:47728655 | A | G | 207 | a0001c0001t0001g0010 a0001c0001t0001g0076 a0001c0001t0001g0136 others(204): Show |
213 | HG00099.hp1 HG00558.hp2 HG00642.hp1 others(210): Show |
intron_variant | MODIFIER | c.915+2431A>G | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47728655 | |||||||
| chr19:47728703 | G | A | 7 | a0001c0002t0006g0003 a0001c0002t0006g0026 a0001c0002t0006g0033 others(4): Show |
8 | HG01243.hp2 HG02109.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.915+2479G>A | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47728703 | |||||||
| chr19:47728735 | A | AT | 21 | a0001c0001t0001g0337 a0001c0001t0010g0300 a0001c0001t0010g0344 others(18): Show |
22 | HG00642.hp1 HG01891.hp1 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.915+2517dupT | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 47728735 | ||||||
| chr19:47728795 | C | T | 5 | a0001c0002t0002g0036 a0002c0007t0007g0290 a0002c0007t0007g0291 others(2): Show |
5 | HG01261.hp2 HG02145.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.915+2571C>T | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47728795 | |||||||
| chr19:47728797 | C | T | 5 | a0001c0001t0001g0197 a0001c0011t0001g0209 a0001c0011t0001g0210 others(2): Show |
5 | HG01070.hp1 HG01071.hp2 HG01256.hp2 others(2): Show |
intron_variant | MODIFIER | c.915+2573C>T | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47728797 | |||||||
| chr19:47728858 | C | T | 136 | a0001c0001t0001g0010 a0001c0001t0001g0144 a0001c0001t0001g0145 others(133): Show |
137 | HG00558.hp2 HG00642.hp2 HG00735.hp2 others(134): Show |
intron_variant | MODIFIER | c.915+2634C>T | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47728858 | |||||||
| chr19:47728862 | A | G | 203 | a0001c0001t0001g0010 a0001c0001t0001g0144 a0001c0001t0001g0145 others(200): Show |
208 | HG00558.hp2 HG00642.hp1 HG00642.hp2 others(205): Show |
intron_variant | MODIFIER | c.915+2638A>G | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47728862 | |||||||
| chr19:47728914 | C | T | 11 | a0001c0004t0002g0043 a0001c0004t0002g0237 a0001c0004t0003g0183 others(8): Show |
11 | HG01074.hp2 HG01891.hp2 HG02040.hp2 others(8): Show |
intron_variant | MODIFIER | c.915+2690C>T | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47728914 | |||||||
| chr19:47728989 | C | T | 130 | a0001c0001t0001g0010 a0001c0001t0001g0144 a0001c0001t0001g0145 others(127): Show |
132 | HG00099.hp1 HG00558.hp2 HG00642.hp2 others(129): Show |
intron_variant | MODIFIER | c.915+2765C>T | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47728989 | |||||||
| chr19:47729181 | C | T | 4 | a0001c0001t0001g0092 a0001c0001t0001g0098 a0001c0001t0001g0114 others(1): Show |
4 | NA18970.hp1 NA18985.hp2 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.915+2957C>T | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47729181 | |||||||
| chr19:47729348 | C | G | 13 | a0001c0001t0010g0300 a0001c0001t0010g0344 a0001c0001t0010g0350 others(10): Show |
13 | HG01074.hp2 HG01884.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.915+3124C>G | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47729348 | |||||||
| chr19:47729460 | C | T | 15 | a0001c0001t0001g0303 a0001c0002t0003g0070 a0001c0002t0004g0059 others(12): Show |
15 | HG01074.hp2 HG01884.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.915+3236C>T | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47729460 | |||||||
| chr19:47729504 | G | A | 7 | a0001c0002t0006g0003 a0001c0002t0006g0026 a0001c0002t0006g0033 others(4): Show |
8 | HG01243.hp2 HG02109.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.915+3280G>A | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47729504 | |||||||
| chr19:47729932 | GCCT | G | 9 | a0001c0002t0002g0036 a0001c0002t0003g0301 a0001c0004t0003g0021 others(6): Show |
9 | HG00738.hp1 HG01261.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.915+3715_915+3717d others(5): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 47729932 | ||||||
| chr19:47730139 | C | T | 1 | a0001c0001t0001g0358 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.915+3915C>T | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47730139 | |||||||
| chr19:47730296 | C | T | 7 | a0001c0002t0006g0003 a0001c0002t0006g0026 a0001c0002t0006g0033 others(4): Show |
8 | HG01243.hp2 HG02109.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.915+4072C>T | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47730296 | |||||||
| chr19:47730514 | CAT | C | 3 | a0001c0001t0010g0300 a0001c0001t0010g0344 a0001c0001t0010g0350 |
3 | HG03195.hp2 HG03209.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.915+4293_915+4294d others(4): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 47730514 | ||||||
| chr19:47730666 | G | T | 3 | a0001c0001t0010g0300 a0001c0001t0010g0344 a0001c0001t0010g0350 |
3 | HG03195.hp2 HG03209.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.915+4442G>T | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47730666 | |||||||
| chr19:47730870 | T | C | 247 | a0001c0001t0001g0019 a0001c0001t0001g0024 a0001c0001t0001g0028 others(244): Show |
251 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(248): Show |
intron_variant | MODIFIER | c.915+4646T>C | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47730870 | |||||||
| chr19:47730925 | T | G | 1 | a0001c0001t0001g0046 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.915+4701T>G | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47730925 | |||||||
| chr19:47731122 | C | T | 11 | a0001c0001t0010g0300 a0001c0001t0010g0344 a0001c0001t0010g0350 others(8): Show |
11 | HG01891.hp1 HG02055.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.915+4898C>T | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47731122 | |||||||
| chr19:47731189 | G | C | 16 | a0001c0001t0001g0303 a0001c0002t0003g0004 a0001c0002t0003g0020 others(13): Show |
18 | HG02055.hp2 HG02258.hp2 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.915+4965G>C | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47731189 | |||||||
| chr19:47731264 | C | CT | 6 | a0001c0001t0001g0083 a0001c0001t0001g0087 a0001c0001t0001g0151 others(3): Show |
6 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(3): Show |
intron_variant | MODIFIER | c.915+5043dupT | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 47731264 | ||||||
| chr19:47731267 | T | TAAAAAAA others(3): Show |
2 | a0001c0008t0005g0341 a0001c0008t0005g0364 |
2 | HG00741.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.915+5047_915+5056d others(12): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 47731267 | ||||||
| chr19:47731267 | T | TTA | 60 | a0001c0001t0001g0046 a0001c0001t0001g0050 a0001c0001t0001g0055 others(57): Show |
60 | HG00438.hp2 HG00544.hp1 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.915+5043_915+5044i others(4): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47731267 | |||||||
| chr19:47731267 | TA | T | 6 | a0001c0001t0001g0177 a0001c0001t0001g0197 a0001c0002t0002g0041 others(3): Show |
6 | HG00738.hp2 HG01256.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.915+5056delA | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 47731267 | ||||||
| chr19:47731267 | TAA | T | 7 | a0001c0002t0004g0059 a0001c0002t0004g0297 a0001c0002t0004g0330 others(4): Show |
7 | HG01070.hp2 HG01884.hp1 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.915+5055_915+5056d others(4): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 47731267 | ||||||
| chr19:47731268 | A | T | 50 | a0001c0001t0001g0048 a0001c0001t0001g0062 a0001c0001t0001g0074 others(47): Show |
50 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(47): Show |
intron_variant | MODIFIER | c.915+5044A>T | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47731268 | |||||||
| chr19:47731278 | A | ATATATAT others(9): Show |
2 | a0001c0002t0004g0147 a0001c0002t0004g0149 |
2 | HG02055.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.915+5054_915+5055i others(18): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47731278 | |||||||
| chr19:47731278 | A | T | 1 | a0001c0002t0004g0038 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.915+5054A>T | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47731278 | |||||||
| chr19:47731279 | A | AAAAAAAA others(19): Show |
1 | a0001c0002t0002g0171 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.915+5056_915+5057i others(28): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 47731279 | ||||||
| chr19:47731279 | A | AAAAAAAA others(26): Show |
1 | a0001c0002t0009g0150 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.915+5056_915+5057i others(35): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 47731279 | ||||||
| chr19:47731279 | A | AAAAAAAA others(23): Show |
1 | a0001c0002t0002g0319 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.915+5056_915+5057i others(32): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 47731279 | ||||||
| chr19:47731279 | A | AAAAAAAA others(15): Show |
1 | a0001c0010t0005g0012 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.915+5056_915+5057i others(24): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 47731279 | ||||||
| chr19:47731279 | A | AAAAAAAA others(25): Show |
1 | a0001c0012t0003g0006 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.915+5056_915+5057i others(34): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 47731279 | ||||||
| chr19:47731279 | A | AAAAAAAA others(22): Show |
1 | a0001c0002t0004g0172 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.915+5056_915+5057i others(31): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 47731279 | ||||||
| chr19:47731279 | A | AAAAAAAA others(12): Show |
2 | a0001c0010t0005g0015 a0001c0010t0005g0284 |
2 | HG02683.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.915+5056_915+5057i others(21): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 47731279 | ||||||
| chr19:47731279 | A | AAAAAAAA others(14): Show |
1 | a0001c0018t0005g0086 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.915+5056_915+5057i others(23): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 47731279 | ||||||
| chr19:47731279 | A | AAAAAAAA others(8): Show |
4 | a0001c0002t0003g0027 a0001c0002t0003g0225 a0001c0002t0003g0288 others(1): Show |
4 | HG02622.hp1 HG02717.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.915+5056_915+5057i others(17): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 47731279 | ||||||
| chr19:47731279 | A | AAAAAAAA others(10): Show |
2 | a0001c0004t0009g0029 a0001c0010t0005g0017 |
2 | HG01243.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.915+5056_915+5057i others(19): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 47731279 | ||||||
| chr19:47731279 | A | AAAAAAAA others(19): Show |
1 | a0001c0004t0003g0183 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.915+5056_915+5057i others(28): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 47731279 | ||||||
| chr19:47731279 | A | AAAAAAAA others(4): Show |
3 | a0001c0008t0005g0363 a0001c0008t0005g0365 a0001c0008t0005g0381 |
3 | HG00099.hp2 HG03831.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.915+5056_915+5057i others(13): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 47731279 | ||||||
| chr19:47731279 | A | AAAAAAAA others(8): Show |
1 | a0001c0002t0003g0289 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.915+5056_915+5057i others(17): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 47731279 | ||||||
| chr19:47731279 | A | AAAAAAAA others(5): Show |
1 | a0001c0010t0016g0011 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.915+5056_915+5057i others(14): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 47731279 | ||||||
| chr19:47731279 | A | AAAAAAAA others(6): Show |
1 | a0001c0002t0017g0298 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.915+5056_915+5057i others(15): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 47731279 | ||||||
| chr19:47731279 | A | AAAAAAAA others(20): Show |
1 | a0001c0002t0003g0292 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.915+5056_915+5057i others(29): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 47731279 | ||||||
| chr19:47731279 | A | AAAAAAAA others(65): Show |
1 | a0001c0001t0001g0096 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.915+5056_915+5057i others(74): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 47731279 | ||||||
| chr19:47731279 | A | AAAAAAAT others(64): Show |
1 | a0001c0001t0001g0111 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.915+5056_915+5057i others(73): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 47731279 | ||||||
| chr19:47731279 | A | AAAAAATA others(3): Show |
1 | a0001c0002t0003g0070 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.915+5056_915+5057i others(12): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 47731279 | ||||||
| chr19:47731279 | A | AAAAATAT others(66): Show |
1 | a0001c0001t0001g0048 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.915+5056_915+5057i others(75): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 47731279 | ||||||
| chr19:47731279 | A | AAAAATAT others(68): Show |
2 | a0001c0001t0001g0113 a0001c0001t0001g0169 |
2 | HG00408.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.915+5056_915+5057i others(77): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 47731279 | ||||||
| chr19:47731279 | A | AAAAATAT others(62): Show |
1 | a0001c0001t0001g0088 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.915+5056_915+5057i others(71): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 47731279 | ||||||
| chr19:47731279 | A | AAAATATA others(65): Show |
1 | a0002c0009t0001g0035 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.915+5056_915+5057i others(74): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 47731279 | ||||||
| chr19:47731279 | A | AAAATATA others(67): Show |
1 | a0001c0001t0001g0024 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.915+5056_915+5057i others(76): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 47731279 | ||||||
| chr19:47731279 | A | AAAATATA others(61): Show |
2 | a0001c0001t0001g0075 a0001c0001t0001g0376 |
2 | HG00408.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.915+5056_915+5057i others(70): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 47731279 | ||||||
| chr19:47731279 | A | AAAATATA others(71): Show |
2 | a0001c0001t0001g0110 a0004c0027t0001g0108 |
2 | NA18950.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.915+5056_915+5057i others(80): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 47731279 | ||||||
| chr19:47731279 | A | AAAATATA others(79): Show |
1 | a0001c0001t0001g0080 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.915+5056_915+5057i others(88): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 47731279 | ||||||
| chr19:47731279 | A | AAAATATA others(67): Show |
1 | a0001c0015t0001g0236 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.915+5056_915+5057i others(76): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 47731279 | ||||||
| chr19:47731279 | A | AAAATTAT others(59): Show |
1 | a0001c0004t0002g0043 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.915+5056_915+5057i others(68): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 47731279 | ||||||
| chr19:47731279 | A | AAAATTAT others(61): Show |
1 | a0001c0015t0001g0104 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.915+5056_915+5057i others(70): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 47731279 | ||||||
| chr19:47731279 | A | AAAATTAT others(61): Show |
1 | a0001c0015t0001g0302 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.915+5056_915+5057i others(70): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 47731279 | ||||||
| chr19:47731279 | A | AAATATAT others(2): Show |
6 | a0001c0002t0003g0020 a0001c0002t0003g0030 a0001c0002t0003g0031 others(3): Show |
6 | HG02055.hp2 HG02451.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.915+5056_915+5057i others(11): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 47731279 | ||||||
| chr19:47731279 | A | AAATATAT others(4): Show |
1 | a0001c0002t0008g0286 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.915+5056_915+5057i others(13): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 47731279 | ||||||
| chr19:47731279 | A | AAATATAT others(18): Show |
1 | a0001c0001t0001g0337 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.915+5056_915+5057i others(27): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 47731279 | ||||||
| chr19:47731279 | A | AAATATAT others(68): Show |
1 | a0001c0001t0001g0375 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.915+5056_915+5057i others(77): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 47731279 | ||||||
| chr19:47731279 | A | AAATTATA others(17): Show |
1 | a0001c0004t0002g0237 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.915+5056_915+5057i others(26): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 47731279 | ||||||
| chr19:47731279 | A | AATATATA others(63): Show |
1 | a0001c0001t0001g0379 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.915+5068_915+5069i others(72): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 47731279 | ||||||
| chr19:47731279 | A | AT | 3 | a0001c0001t0001g0229 a0001c0002t0002g0127 a0001c0002t0002g0305 |
3 | HG04199.hp1 NA18995.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.915+5055_915+5056i others(3): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47731279 | |||||||
| chr19:47731279 | A | ATATATAT others(72): Show |
1 | a0001c0001t0001g0371 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.915+5055_915+5056i others(81): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47731279 | |||||||
| chr19:47731279 | A | ATATATAT others(66): Show |
1 | a0001c0001t0001g0274 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.915+5055_915+5056i others(75): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47731279 | |||||||
| chr19:47731279 | A | ATATATAT others(10): Show |
1 | a0001c0002t0004g0038 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.915+5055_915+5056i others(19): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47731279 | |||||||
| chr19:47731279 | A | ATATATAT others(60): Show |
1 | a0001c0001t0001g0061 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.915+5055_915+5056i others(69): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47731279 | |||||||
| chr19:47731279 | A | ATTATATA others(53): Show |
1 | a0001c0001t0010g0300 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.915+5055_915+5056i others(62): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47731279 | |||||||
| chr19:47731279 | A | ATTATATA others(51): Show |
1 | a0001c0001t0010g0350 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.915+5055_915+5056i others(60): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47731279 | |||||||
| chr19:47731279 | A | ATTATATA others(89): Show |
1 | a0001c0001t0010g0344 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.915+5055_915+5056i others(98): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47731279 | |||||||
| chr19:47731279 | A | T | 25 | a0001c0001t0001g0123 a0001c0001t0001g0165 a0001c0001t0013g0072 others(22): Show |
25 | HG00140.hp2 HG01256.hp1 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.915+5055A>T | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47731279 | |||||||
| chr19:47731279 | AAT | A | 9 | a0001c0001t0001g0173 a0001c0001t0001g0313 a0001c0002t0002g0166 others(6): Show |
9 | HG00642.hp1 HG00735.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.916-5068_916-5067d others(4): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 47731279 | ||||||
| chr19:47731279 | AATAT | A | 6 | a0001c0001t0001g0314 a0001c0002t0002g0322 a0001c0004t0003g0021 others(3): Show |
6 | HG00738.hp1 HG01168.hp2 HG02523.hp2 others(3): Show |
intron_variant | MODIFIER | c.916-5070_916-5067d others(6): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 47731279 | ||||||
| chr19:47731280 | A | AAAAAATA others(64): Show |
1 | a0001c0001t0001g0112 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.915+5056_915+5057i others(73): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47731280 | |||||||
| chr19:47731280 | A | AAAAATAT others(63): Show |
2 | a0001c0001t0001g0119 a0001c0001t0001g0196 |
2 | HG02155.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.915+5056_915+5057i others(72): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47731280 | |||||||
| chr19:47731280 | A | AAAAATAT others(63): Show |
10 | a0001c0001t0001g0078 a0001c0001t0001g0103 a0001c0001t0001g0116 others(7): Show |
10 | HG00423.hp2 HG00639.hp2 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.915+5056_915+5057i others(72): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47731280 | |||||||
| chr19:47731280 | A | AAAAATAT others(61): Show |
1 | a0001c0001t0001g0189 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.915+5056_915+5057i others(70): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47731280 | |||||||
| chr19:47731280 | A | AAAAATAT others(63): Show |
1 | a0001c0001t0001g0218 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.915+5056_915+5057i others(72): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47731280 | |||||||
| chr19:47731280 | A | AAAATATA others(46): Show |
1 | a0001c0001t0001g0101 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.915+5056_915+5057i others(55): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47731280 | |||||||
| chr19:47731280 | A | AAAATATA others(66): Show |
1 | a0001c0001t0001g0081 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.915+5056_915+5057i others(75): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47731280 | |||||||
| chr19:47731280 | A | AAAATATA others(62): Show |
1 | a0001c0001t0001g0089 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.915+5056_915+5057i others(71): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47731280 | |||||||
| chr19:47731280 | A | AAAATATA others(64): Show |
1 | a0001c0001t0001g0074 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.915+5056_915+5057i others(73): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47731280 | |||||||
| chr19:47731280 | A | AAAATATA others(62): Show |
1 | a0001c0001t0001g0368 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.915+5056_915+5057i others(71): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47731280 | |||||||
| chr19:47731280 | A | AAAATATA others(60): Show |
2 | a0001c0001t0001g0242 a0001c0001t0001g0336 |
2 | HG01934.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.915+5056_915+5057i others(69): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47731280 | |||||||
| chr19:47731280 | A | AAATATAT others(61): Show |
1 | a0001c0001t0001g0382 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.915+5056_915+5057i others(70): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47731280 | |||||||
| chr19:47731280 | A | AAATATAT others(59): Show |
1 | a0001c0001t0001g0373 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.915+5056_915+5057i others(68): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47731280 | |||||||
| chr19:47731280 | A | AAATATAT others(63): Show |
1 | a0001c0001t0001g0356 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.915+5056_915+5057i others(72): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47731280 | |||||||
| chr19:47731280 | A | AAATATAT others(65): Show |
1 | a0001c0001t0001g0191 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.915+5056_915+5057i others(74): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47731280 | |||||||
| chr19:47731280 | A | AATATATA others(62): Show |
2 | a0001c0001t0001g0270 a0001c0001t0001g0271 |
2 | HG03239.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.915+5056_915+5057i others(71): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47731280 | |||||||
| chr19:47731280 | A | ATATATAT others(7): Show |
5 | a0001c0002t0004g0064 a0001c0002t0004g0146 a0001c0002t0004g0148 others(2): Show |
5 | HG01891.hp1 HG02896.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.915+5069_915+5070i others(16): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 47731280 | ||||||
| chr19:47731280 | AT | A | 49 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0235 others(46): Show |
49 | HG00642.hp2 HG01069.hp1 HG01070.hp1 others(46): Show |
intron_variant | MODIFIER | c.915+5057delT | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47731280 | |||||||
| chr19:47731280 | ATAT | A | 6 | a0001c0001t0001g0328 a0001c0003t0002g0324 a0001c0003t0002g0327 others(3): Show |
6 | HG00099.hp1 HG01169.hp1 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.915+5057_915+5059d others(5): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47731280 | |||||||
| chr19:47731280 | ATATAT | A | 3 | a0001c0002t0006g0003 a0001c0002t0006g0026 a0001c0002t0006g0304 |
3 | HG02280.hp1 HG03579.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.915+5057_915+5061d others(7): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47731280 | |||||||
| chr19:47731281 | T | A | 25 | a0001c0001t0001g0010 a0001c0002t0002g0001 a0001c0002t0002g0047 others(22): Show |
26 | HG01167.hp1 HG01169.hp2 HG01361.hp1 others(23): Show |
intron_variant | MODIFIER | c.915+5057T>A | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47731281 | |||||||
| chr19:47731283 | T | A | 42 | a0001c0001t0001g0010 a0001c0001t0001g0173 a0001c0001t0001g0313 others(39): Show |
42 | HG00642.hp1 HG00735.hp2 HG01070.hp1 others(39): Show |
intron_variant | MODIFIER | c.915+5059T>A | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47731283 | |||||||
| chr19:47731285 | T | A | 3 | a0001c0002t0002g0322 a0001c0002t0003g0282 a0001c0003t0002g0362 |
3 | HG02523.hp2 HG02572.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.915+5061T>A | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47731285 | |||||||
| chr19:47731287 | T | A | 3 | a0001c0002t0006g0003 a0001c0002t0006g0026 a0001c0002t0006g0304 |
4 | HG01243.hp2 HG02280.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.915+5063T>A | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47731287 | |||||||
| chr19:47731287 | T | C | 1 | a0001c0004t0002g0237 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.915+5063T>C | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47731287 | |||||||
| chr19:47731291 | T | C | 3 | a0001c0004t0002g0043 a0001c0015t0001g0104 a0001c0015t0001g0302 |
3 | HG01074.hp2 HG02040.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.915+5067T>C | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47731291 | |||||||
| chr19:47731292 | A | G | 2 | a0001c0001t0001g0219 a0001c0001t0001g0347 |
2 | HG02630.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.915+5068A>G | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47731292 | |||||||
| chr19:47731293 | T | C | 3 | a0001c0004t0003g0183 a0001c0010t0005g0012 a0001c0018t0005g0086 |
3 | HG00280.hp1 HG01255.hp1 HG01891.hp2 |
intron_variant | MODIFIER | c.915+5069T>C | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47731293 | |||||||
| chr19:47731294 | A | G | 66 | a0001c0001t0001g0046 a0001c0001t0001g0050 a0001c0001t0001g0055 others(63): Show |
66 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.915+5070A>G | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47731294 | |||||||
| chr19:47731295 | T | C | 11 | a0001c0001t0001g0024 a0001c0001t0001g0096 a0001c0001t0001g0337 others(8): Show |
12 | HG00323.hp1 HG01243.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.915+5071T>C | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47731295 | |||||||
| chr19:47731295 | T | TATGTATA others(73): Show |
1 | a0001c0001t0001g0083 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.916-5072_916-5071i others(82): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 47731295 | ||||||
| chr19:47731295 | T | TGTATATA others(67): Show |
1 | a0001c0001t0013g0072 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.915+5071_915+5072i others(76): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47731295 | |||||||
| chr19:47731295 | T | TGTATATA others(67): Show |
1 | a0001c0001t0001g0123 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.915+5071_915+5072i others(76): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47731295 | |||||||
| chr19:47731295 | T | TGTATATA others(69): Show |
9 | a0001c0001t0001g0058 a0001c0001t0001g0066 a0001c0001t0001g0087 others(6): Show |
9 | HG01081.hp1 HG01496.hp1 HG02083.hp2 others(6): Show |
intron_variant | MODIFIER | c.915+5071_915+5072i others(78): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47731295 | |||||||
| chr19:47731295 | T | TGTATATA others(71): Show |
5 | a0001c0001t0001g0133 a0001c0001t0001g0135 a0001c0001t0001g0355 others(2): Show |
5 | NA18942.hp1 NA18955.hp1 NA18955.hp2 others(2): Show |
intron_variant | MODIFIER | c.915+5071_915+5072i others(80): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47731295 | |||||||
| chr19:47731295 | T | TGTATATA others(73): Show |
1 | a0001c0001t0001g0068 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.915+5071_915+5072i others(82): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47731295 | |||||||
| chr19:47731295 | T | TGTATATA others(71): Show |
1 | a0001c0001t0001g0378 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.915+5071_915+5072i others(80): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47731295 | |||||||
| chr19:47731295 | T | TGTATATA others(71): Show |
10 | a0001c0001t0001g0019 a0001c0001t0001g0028 a0001c0001t0001g0277 others(7): Show |
10 | HG00280.hp2 HG00639.hp1 HG01069.hp2 others(7): Show |
intron_variant | MODIFIER | c.915+5071_915+5072i others(80): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47731295 | |||||||
| chr19:47731295 | T | TGTATATA others(75): Show |
1 | a0001c0001t0001g0153 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.915+5071_915+5072i others(84): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47731295 | |||||||
| chr19:47731295 | T | TGTATATA others(77): Show |
2 | a0001c0001t0001g0094 a0001c0001t0001g0109 |
2 | NA19054.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.915+5071_915+5072i others(86): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47731295 | |||||||
| chr19:47731295 | T | TGTATATA others(65): Show |
1 | a0001c0001t0001g0268 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.915+5071_915+5072i others(74): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47731295 | |||||||
| chr19:47731295 | T | TGTATATA others(67): Show |
1 | a0001c0001t0001g0102 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.915+5071_915+5072i others(76): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47731295 | |||||||
| chr19:47731295 | T | TGTATATA others(69): Show |
5 | a0001c0001t0001g0062 a0001c0001t0001g0100 a0001c0001t0001g0141 others(2): Show |
5 | HG01175.hp1 HG01258.hp1 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.915+5071_915+5072i others(78): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47731295 | |||||||
| chr19:47731295 | T | TGTATATA others(71): Show |
2 | a0001c0001t0001g0357 a0001c0001t0001g0380 |
2 | HG00423.hp1 NA18954.hp2 |
intron_variant | MODIFIER | c.915+5071_915+5072i others(80): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47731295 | |||||||
| chr19:47731295 | T | TGTATATA others(73): Show |
1 | a0001c0001t0001g0317 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.915+5071_915+5072i others(82): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47731295 | |||||||
| chr19:47731296 | A | G | 1 | a0001c0001t0001g0215 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.915+5072A>G | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47731296 | |||||||
| chr19:47731299 | T | C | 1 | a0001c0001t0001g0274 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.916-5070T>C | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47731299 | |||||||
| chr19:47731300 | A | ATATATAT others(39): Show |
1 | a0001c0001t0001g0219 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.916-5067_916-5066i others(48): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 47731300 | ||||||
| chr19:47731301 | T | C | 6 | a0001c0002t0002g0171 a0001c0002t0002g0319 a0001c0002t0004g0038 others(3): Show |
6 | HG01192.hp1 HG02572.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.916-5068T>C | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47731301 | |||||||
| chr19:47731303 | C | CAT | 11 | a0001c0001t0010g0300 a0001c0001t0010g0344 a0001c0001t0010g0350 others(8): Show |
11 | HG01891.hp1 HG02055.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.916-5056_916-5055d others(4): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 47731303 | ||||||
| chr19:47731303 | C | CATATATA others(1): Show |
11 | a0001c0002t0003g0027 a0001c0002t0003g0225 a0001c0002t0003g0288 others(8): Show |
11 | HG02622.hp1 HG02630.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.916-5062_916-5055d others(10): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 47731303 | ||||||
| chr19:47731303 | C | CATATATA others(3): Show |
5 | a0001c0008t0005g0341 a0001c0008t0005g0363 a0001c0008t0005g0364 others(2): Show |
5 | HG00099.hp2 HG00741.hp1 HG01346.hp2 others(2): Show |
intron_variant | MODIFIER | c.916-5064_916-5055d others(12): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 47731303 | ||||||
| chr19:47731303 | C | CATATATA others(7): Show |
1 | a0001c0024t0001g0329 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.916-5055_916-5054i others(16): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 47731303 | ||||||
| chr19:47731303 | C | T | 133 | a0001c0001t0001g0019 a0001c0001t0001g0024 a0001c0001t0001g0028 others(130): Show |
134 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.916-5066C>T | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47731303 | |||||||
| chr19:47731304 | A | ATATATAT others(71): Show |
1 | a0001c0001t0001g0128 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.916-5057_916-5056i others(80): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 47731304 | ||||||
| chr19:47731304 | A | ATATATAT others(67): Show |
1 | a0001c0001t0001g0082 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.916-5057_916-5056i others(76): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 47731304 | ||||||
| chr19:47731304 | A | ATATATAT others(69): Show |
1 | a0001c0001t0001g0261 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.916-5055_916-5054i others(78): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 47731304 | ||||||
| chr19:47731304 | A | ATATATAT others(67): Show |
5 | a0001c0001t0001g0055 a0001c0001t0001g0090 a0001c0013t0001g0018 others(2): Show |
5 | HG01074.hp1 HG02015.hp2 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.916-5055_916-5054i others(76): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 47731304 | ||||||
| chr19:47731304 | A | ATATATAT others(65): Show |
2 | a0001c0001t0001g0224 a0001c0001t0001g0372 |
2 | HG02602.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.916-5055_916-5054i others(74): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 47731304 | ||||||
| chr19:47731304 | A | ATATATAT others(71): Show |
1 | a0001c0001t0001g0093 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.916-5055_916-5054i others(80): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 47731304 | ||||||
| chr19:47731304 | A | ATATATAT others(69): Show |
1 | a0001c0001t0001g0046 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.916-5055_916-5054i others(78): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 47731304 | ||||||
| chr19:47731304 | A | ATATATAT others(67): Show |
1 | a0001c0001t0001g0267 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.916-5055_916-5054i others(76): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 47731304 | ||||||
| chr19:47731304 | A | ATATATAT others(109): Show |
1 | a0001c0001t0001g0057 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.916-5055_916-5054i others(118): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 47731304 | ||||||
| chr19:47731304 | A | ATATATAT others(69): Show |
28 | a0001c0001t0001g0073 a0001c0001t0001g0076 a0001c0001t0001g0097 others(25): Show |
28 | HG00438.hp1 HG01109.hp1 HG01167.hp2 others(25): Show |
intron_variant | MODIFIER | c.916-5055_916-5054i others(78): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 47731304 | ||||||
| chr19:47731304 | A | ATATATAT others(69): Show |
1 | a0001c0001t0018g0044 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.916-5055_916-5054i others(78): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 47731304 | ||||||
| chr19:47731304 | A | ATATATAT others(71): Show |
1 | a0001c0001t0001g0125 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.916-5055_916-5054i others(80): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 47731304 | ||||||
| chr19:47731304 | A | ATATATAT others(73): Show |
1 | a0001c0001t0001g0152 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.916-5055_916-5054i others(82): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 47731304 | ||||||
| chr19:47731304 | A | ATATATAT others(69): Show |
2 | a0001c0001t0001g0095 a0001c0019t0001g0134 |
2 | HG01934.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.916-5055_916-5054i others(78): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 47731304 | ||||||
| chr19:47731304 | A | ATATATAT others(65): Show |
3 | a0001c0001t0001g0092 a0001c0001t0001g0114 a0001c0001t0001g0115 |
3 | NA18970.hp1 NA19005.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.916-5055_916-5054i others(74): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 47731304 | ||||||
| chr19:47731304 | A | ATATATAT others(67): Show |
5 | a0001c0001t0001g0050 a0001c0001t0001g0056 a0001c0001t0001g0084 others(2): Show |
5 | HG00438.hp2 HG01106.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.916-5055_916-5054i others(76): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 47731304 | ||||||
| chr19:47731304 | A | ATATATAT others(71): Show |
1 | a0001c0001t0001g0151 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.916-5055_916-5054i others(80): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 47731304 | ||||||
| chr19:47731304 | A | ATATATAT others(59): Show |
1 | a0001c0001t0001g0255 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.916-5055_916-5054i others(68): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 47731304 | ||||||
| chr19:47731304 | A | ATATATAT others(61): Show |
1 | a0001c0001t0001g0117 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.916-5055_916-5054i others(70): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 47731304 | ||||||
| chr19:47731304 | A | ATATATAT others(73): Show |
1 | a0001c0020t0001g0045 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.916-5055_916-5054i others(82): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 47731304 | ||||||
| chr19:47731304 | A | ATATATAT others(53): Show |
1 | a0001c0001t0001g0106 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.916-5055_916-5054i others(62): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 47731304 | ||||||
| chr19:47731304 | A | ATATATAT others(69): Show |
1 | a0006c0021t0001g0085 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.916-5055_916-5054i others(78): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 47731304 | ||||||
| chr19:47731304 | A | ATATATAT others(71): Show |
2 | a0001c0001t0001g0129 a0001c0001t0001g0154 |
2 | HG02135.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.916-5055_916-5054i others(80): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 47731304 | ||||||
| chr19:47731304 | A | ATATATAT others(69): Show |
1 | a0001c0001t0001g0190 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.916-5055_916-5054i others(78): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 47731304 | ||||||
| chr19:47731304 | A | ATATATAT others(77): Show |
1 | a0001c0001t0001g0238 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.916-5055_916-5054i others(86): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 47731304 | ||||||
| chr19:47731304 | A | ATATATAT others(79): Show |
1 | a0001c0001t0001g0266 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.916-5055_916-5054i others(88): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 47731304 | ||||||
| chr19:47731304 | A | ATATATAT others(1): Show |
37 | a0001c0001t0001g0048 a0001c0001t0001g0061 a0001c0001t0001g0074 others(34): Show |
37 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(34): Show |
intron_variant | MODIFIER | c.916-5058_916-5057i others(10): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 47731304 | ||||||
| chr19:47731304 | A | G | 48 | a0001c0001t0001g0019 a0001c0001t0001g0024 a0001c0001t0001g0028 others(45): Show |
48 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(45): Show |
intron_variant | MODIFIER | c.916-5065A>G | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47731304 | |||||||
| chr19:47731308 | A | G | 1 | a0001c0001t0001g0274 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.916-5061A>G | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47731308 | |||||||
| chr19:47731312 | A | ATACATAT others(69): Show |
1 | a0001c0001t0001g0279 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.916-5055_916-5054i others(78): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 47731312 | ||||||
| chr19:47731312 | A | G | 1 | a0001c0001t0001g0354 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.916-5057A>G | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47731312 | |||||||
| chr19:47731313 | T | TATACATA others(70): Show |
1 | a0001c0001t0001g0215 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.916-5055_916-5054i others(79): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 47731313 | ||||||
| chr19:47731314 | A | ATATAT | 4 | a0001c0002t0002g0171 a0001c0002t0002g0319 a0001c0002t0004g0172 others(1): Show |
4 | HG02572.hp2 HG02886.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.916-5055_916-5054i others(7): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47731314 | |||||||
| chr19:47731315 | A | T | 1 | a0001c0001t0001g0215 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.916-5054A>T | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47731315 | |||||||
| chr19:47731315 | AT | A | 9 | a0001c0001t0001g0314 a0001c0001t0001g0328 a0001c0003t0002g0005 others(6): Show |
10 | HG00099.hp1 HG01168.hp2 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.916-5041delT | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 47731315 | ||||||
| chr19:47731316 | T | A | 5 | a0001c0001t0001g0354 a0001c0002t0002g0171 a0001c0002t0002g0319 others(2): Show |
5 | HG02572.hp2 HG02886.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.916-5053T>A | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47731316 | |||||||
| chr19:47731353 | A | G | 1 | a0005c0017t0014g0206 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.916-5016A>G | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47731353 | |||||||
| chr19:47731467 | A | G | 2 | a0001c0001t0001g0260 a0001c0001t0001g0261 |
2 | NA18983.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.916-4902A>G | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47731467 | |||||||
| chr19:47731485 | T | A | 1 | a0005c0017t0014g0206 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.916-4884T>A | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47731485 | |||||||
| chr19:47731634 | T | C | 1 | a0001c0001t0001g0303 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.916-4735T>C | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47731634 | |||||||
| chr19:47731785 | A | AT | 183 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0024 others(180): Show |
183 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.916-4564dupT | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 47731785 | ||||||
| chr19:47731785 | A | ATT | 37 | a0001c0001t0001g0046 a0001c0001t0001g0055 a0001c0001t0001g0057 others(34): Show |
37 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(34): Show |
intron_variant | MODIFIER | c.916-4565_916-4564d others(4): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 47731785 | ||||||
| chr19:47731785 | A | ATTT | 8 | a0001c0001t0001g0093 a0001c0001t0001g0277 a0001c0002t0002g0323 others(5): Show |
9 | HG01175.hp2 HG01243.hp2 HG02074.hp1 others(6): Show |
intron_variant | MODIFIER | c.916-4566_916-4564d others(5): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 47731785 | ||||||
| chr19:47731785 | AT | A | 12 | a0001c0002t0003g0320 a0001c0004t0002g0043 a0001c0004t0002g0237 others(9): Show |
12 | HG00738.hp1 HG01074.hp2 HG02040.hp2 others(9): Show |
intron_variant | MODIFIER | c.916-4564delT | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 47731785 | ||||||
| chr19:47731826 | C | T | 3 | a0001c0004t0002g0043 a0001c0015t0001g0104 a0001c0015t0001g0302 |
3 | HG01074.hp2 HG02040.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.916-4543C>T | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47731826 | |||||||
| chr19:47731873 | C | T | 1 | a0001c0001t0001g0303 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.916-4496C>T | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47731873 | |||||||
| chr19:47731900 | G | A | 2 | a0001c0002t0002g0233 a0001c0002t0002g0239 |
2 | HG02056.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.916-4469G>A | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47731900 | |||||||
| chr19:47732065 | G | A | 2 | a0001c0001t0001g0154 a0001c0013t0001g0018 |
2 | HG02735.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.916-4304G>A | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47732065 | |||||||
| chr19:47732182 | C | T | 1 | a0001c0004t0006g0272 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.916-4187C>T | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47732182 | |||||||
| chr19:47732277 | C | T | 7 | a0001c0002t0003g0301 a0001c0004t0003g0021 a0001c0004t0003g0022 others(4): Show |
7 | HG00738.hp1 HG02145.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.916-4092C>T | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47732277 | |||||||
| chr19:47732280 | G | A | 11 | a0001c0008t0005g0341 a0001c0008t0005g0363 a0001c0008t0005g0364 others(8): Show |
11 | HG00099.hp2 HG00280.hp1 HG00741.hp1 others(8): Show |
intron_variant | MODIFIER | c.916-4089G>A | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47732280 | |||||||
| chr19:47732281 | G | C | 1 | a0001c0020t0001g0045 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.916-4088G>C | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47732281 | |||||||
| chr19:47732361 | G | A | 1 | a0001c0015t0001g0104 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.916-4008G>A | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47732361 | |||||||
| chr19:47732398 | C | T | 10 | a0001c0008t0005g0341 a0001c0008t0005g0363 a0001c0008t0005g0364 others(7): Show |
10 | HG00099.hp2 HG00280.hp1 HG00741.hp1 others(7): Show |
intron_variant | MODIFIER | c.916-3971C>T | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47732398 | |||||||
| chr19:47732409 | G | A | 1 | a0001c0002t0002g0174 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.916-3960G>A | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47732409 | |||||||
| chr19:47732458 | G | C | 1 | a0001c0004t0006g0272 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.916-3911G>C | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47732458 | |||||||
| chr19:47732568 | C | T | 1 | a0006c0021t0001g0085 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.916-3801C>T | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47732568 | |||||||
| chr19:47732590 | T | A | 11 | a0001c0001t0010g0300 a0001c0001t0010g0344 a0001c0001t0010g0350 others(8): Show |
11 | HG01891.hp1 HG02055.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.916-3779T>A | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47732590 | |||||||
| chr19:47732644 | C | A | 26 | a0001c0001t0001g0303 a0001c0002t0003g0004 a0001c0002t0003g0020 others(23): Show |
28 | HG01884.hp1 HG01884.hp2 HG02055.hp2 others(25): Show |
intron_variant | MODIFIER | c.916-3725C>A | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47732644 | |||||||
| chr19:47732858 | C | A | 4 | a0001c0002t0002g0171 a0001c0002t0002g0319 a0001c0002t0004g0172 others(1): Show |
4 | HG02572.hp2 HG02886.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.916-3511C>A | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47732858 | |||||||
| chr19:47732859 | G | A | 2 | a0001c0002t0003g0292 a0001c0012t0003g0006 |
3 | HG02615.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.916-3510G>A | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47732859 | |||||||
| chr19:47732888 | A | T | 1 | a0001c0002t0002g0193 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.916-3481A>T | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47732888 | |||||||
| chr19:47732896 | C | A | 1 | a0005c0017t0014g0206 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.916-3473C>A | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47732896 | |||||||
| chr19:47732897 | A | C | 1 | a0005c0017t0014g0206 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.916-3472A>C | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47732897 | |||||||
| chr19:47732928 | A | G | 8 | a0001c0002t0004g0038 a0001c0002t0004g0064 a0001c0002t0004g0146 others(5): Show |
8 | HG01891.hp1 HG02055.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.916-3441A>G | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47732928 | |||||||
| chr19:47733056 | C | T | 15 | a0001c0001t0001g0303 a0001c0002t0003g0004 a0001c0002t0003g0020 others(12): Show |
17 | HG02055.hp2 HG02258.hp2 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.916-3313C>T | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47733056 | |||||||
| chr19:47733082 | C | CA | 185 | a0001c0001t0001g0019 a0001c0001t0001g0024 a0001c0001t0001g0028 others(182): Show |
186 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.916-3277dupA | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 47733082 | ||||||
| chr19:47733093 | T | A | 18 | a0001c0001t0001g0222 a0001c0001t0001g0226 a0001c0002t0002g0312 others(15): Show |
20 | HG00639.hp2 HG01099.hp1 HG01358.hp2 others(17): Show |
intron_variant | MODIFIER | c.916-3276T>A | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47733093 | |||||||
| chr19:47733224 | A | T | 1 | a0001c0001t0001g0354 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.916-3145A>T | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47733224 | |||||||
| chr19:47733227 | C | T | 19 | a0001c0001t0001g0314 a0001c0001t0001g0328 a0001c0002t0002g0007 others(16): Show |
20 | HG00099.hp1 HG00642.hp1 HG01070.hp2 others(17): Show |
intron_variant | MODIFIER | c.916-3142C>T | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47733227 | |||||||
| chr19:47733231 | C | T | 8 | a0001c0002t0004g0038 a0001c0002t0004g0064 a0001c0002t0004g0146 others(5): Show |
8 | HG01891.hp1 HG02055.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.916-3138C>T | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47733231 | |||||||
| chr19:47733240 | CT | C | 17 | a0001c0001t0001g0058 a0001c0001t0001g0118 a0001c0002t0002g0247 others(14): Show |
17 | HG00099.hp2 HG00280.hp1 HG00741.hp1 others(14): Show |
intron_variant | MODIFIER | c.916-3116delT | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 47733240 | ||||||
| chr19:47733386 | A | T | 246 | a0001c0001t0001g0019 a0001c0001t0001g0024 a0001c0001t0001g0028 others(243): Show |
250 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(247): Show |
intron_variant | MODIFIER | c.916-2983A>T | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47733386 | |||||||
| chr19:47733408 | T | C | 19 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0173 others(16): Show |
19 | HG00735.hp2 HG00738.hp2 HG01069.hp1 others(16): Show |
intron_variant | MODIFIER | c.916-2961T>C | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47733408 | |||||||
| chr19:47733445 | G | A | 18 | a0001c0001t0010g0300 a0001c0001t0010g0344 a0001c0001t0010g0350 others(15): Show |
19 | HG01243.hp2 HG01891.hp1 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.916-2924G>A | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47733445 | |||||||
| chr19:47733449 | G | A | 193 | a0001c0001t0001g0019 a0001c0001t0001g0024 a0001c0001t0001g0028 others(190): Show |
194 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(191): Show |
intron_variant | MODIFIER | c.916-2920G>A | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47733449 | |||||||
| chr19:47733524 | T | A | 9 | a0001c0002t0002g0036 a0001c0002t0003g0301 a0001c0004t0003g0021 others(6): Show |
9 | HG00738.hp1 HG01261.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.916-2845T>A | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47733524 | |||||||
| chr19:47733527 | C | A | 1 | a0001c0001t0001g0354 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.916-2842C>A | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47733527 | |||||||
| chr19:47733615 | C | T | 1 | a0001c0002t0002g0322 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.916-2754C>T | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47733615 | |||||||
| chr19:47733645 | C | T | 2 | a0001c0001t0001g0089 a0001c0001t0001g0090 |
2 | HG01074.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.916-2724C>T | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47733645 | |||||||
| chr19:47733669 | A | AAAAT | 4 | a0001c0001t0001g0197 a0001c0002t0002g0204 a0001c0002t0002g0239 others(1): Show |
4 | HG01256.hp1 HG02451.hp1 NA19063.hp2 others(1): Show |
intron_variant | MODIFIER | c.916-2676_916-2673d others(6): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 47733669 | ||||||
| chr19:47733669 | AAAATAAA others(1): Show |
A | 5 | a0001c0004t0007g0063 a0001c0004t0007g0065 a0001c0004t0007g0361 others(2): Show |
5 | HG02630.hp2 HG02970.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.916-2680_916-2673d others(10): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 47733669 | ||||||
| chr19:47733751 | C | CA | 45 | a0001c0001t0001g0010 a0001c0001t0001g0090 a0001c0001t0010g0300 others(42): Show |
46 | HG01074.hp1 HG01975.hp1 HG02027.hp1 others(43): Show |
intron_variant | MODIFIER | c.916-2594dupA | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 47733751 | ||||||
| chr19:47733751 | C | CAA | 14 | a0001c0001t0010g0344 a0001c0002t0002g0140 a0001c0002t0002g0163 others(11): Show |
14 | HG00642.hp2 HG01261.hp1 HG01928.hp1 others(11): Show |
intron_variant | MODIFIER | c.916-2595_916-2594d others(4): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 47733751 | ||||||
| chr19:47733751 | C | CAAA | 12 | a0001c0002t0006g0003 a0001c0002t0006g0026 a0001c0002t0006g0033 others(9): Show |
13 | HG00099.hp2 HG00280.hp1 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.916-2596_916-2594d others(5): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 47733751 | ||||||
| chr19:47733751 | C | CAAAA | 22 | a0001c0002t0003g0027 a0001c0002t0003g0225 a0001c0002t0003g0288 others(19): Show |
22 | HG00741.hp1 HG01243.hp1 HG01346.hp2 others(19): Show |
intron_variant | MODIFIER | c.916-2597_916-2594d others(6): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 47733751 | ||||||
| chr19:47733751 | C | CAAAAA | 6 | a0001c0001t0001g0337 a0001c0002t0004g0147 a0001c0002t0004g0148 others(3): Show |
7 | HG01891.hp1 HG02055.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.916-2598_916-2594d others(7): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 47733751 | ||||||
| chr19:47733751 | C | CAAAAAAA others(3): Show |
12 | a0001c0001t0001g0068 a0001c0001t0001g0075 a0001c0001t0001g0133 others(9): Show |
12 | HG00408.hp2 HG00544.hp2 HG02083.hp2 others(9): Show |
intron_variant | MODIFIER | c.916-2603_916-2594d others(12): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 47733751 | ||||||
| chr19:47733751 | C | CAAAAAAA others(4): Show |
18 | a0001c0001t0001g0019 a0001c0001t0001g0024 a0001c0001t0001g0028 others(15): Show |
18 | HG00280.hp2 HG00423.hp1 HG01496.hp1 others(15): Show |
intron_variant | MODIFIER | c.916-2604_916-2594d others(13): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 47733751 | ||||||
| chr19:47733751 | C | CAAAAAAA others(5): Show |
36 | a0001c0001t0001g0057 a0001c0001t0001g0094 a0001c0001t0001g0115 others(33): Show |
36 | HG00140.hp2 HG00323.hp1 HG01081.hp2 others(33): Show |
intron_variant | MODIFIER | c.916-2605_916-2594d others(14): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 47733751 | ||||||
| chr19:47733751 | C | CAAAAAAA others(6): Show |
57 | a0001c0001t0001g0046 a0001c0001t0001g0048 a0001c0001t0001g0050 others(54): Show |
57 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(54): Show |
intron_variant | MODIFIER | c.916-2606_916-2594d others(15): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 47733751 | ||||||
| chr19:47733751 | C | CAAAAAAA others(7): Show |
16 | a0001c0001t0001g0056 a0001c0001t0001g0084 a0001c0001t0001g0087 others(13): Show |
16 | HG00438.hp2 HG00558.hp1 HG00639.hp1 others(13): Show |
intron_variant | MODIFIER | c.916-2607_916-2594d others(16): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 47733751 | ||||||
| chr19:47733751 | C | CAAAAAAA others(8): Show |
8 | a0001c0001t0001g0055 a0001c0001t0001g0074 a0001c0001t0001g0076 others(5): Show |
8 | HG00673.hp1 HG01358.hp2 HG02015.hp2 others(5): Show |
intron_variant | MODIFIER | c.916-2608_916-2594d others(17): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 47733751 | ||||||
| chr19:47733751 | C | CAAAAAAA others(9): Show |
4 | a0001c0001t0001g0112 a0001c0001t0001g0211 a0001c0001t0001g0372 others(1): Show |
4 | HG02602.hp1 HG03239.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.916-2609_916-2594d others(18): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 47733751 | ||||||
| chr19:47733751 | C | CAAAAAAA others(10): Show |
1 | a0001c0001t0001g0078 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.916-2610_916-2594d others(19): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 47733751 | ||||||
| chr19:47733751 | CA | C | 46 | a0001c0001t0001g0145 a0001c0001t0001g0173 a0001c0001t0001g0177 others(43): Show |
47 | HG00099.hp1 HG00735.hp2 HG00738.hp1 others(44): Show |
intron_variant | MODIFIER | c.916-2594delA | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 47733751 | ||||||
| chr19:47733775 | A | T | 1 | a0005c0017t0014g0206 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.916-2594A>T | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47733775 | |||||||
| chr19:47733776 | T | C | 1 | a0005c0017t0014g0206 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.916-2593T>C | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47733776 | |||||||
| chr19:47733822 | G | A | 1 | a0001c0002t0002g0143 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.916-2547G>A | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47733822 | |||||||
| chr19:47733829 | G | A | 1 | a0001c0001t0001g0062 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.916-2540G>A | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47733829 | |||||||
| chr19:47733903 | T | C | 1 | a0001c0001t0001g0103 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.916-2466T>C | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47733903 | |||||||
| chr19:47734196 | G | A | 1 | a0001c0002t0004g0038 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.916-2173G>A | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47734196 | |||||||
| chr19:47734304 | C | G | 1 | a0001c0003t0002g0008 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.916-2065C>G | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47734304 | |||||||
| chr19:47734341 | G | C | 1 | a0001c0001t0001g0376 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.916-2028G>C | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47734341 | |||||||
| chr19:47734392 | A | G | 1 | a0001c0004t0006g0272 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.916-1977A>G | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47734392 | |||||||
| chr19:47734870 | T | C | 1 | a0001c0001t0001g0095 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.916-1499T>C | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47734870 | |||||||
| chr19:47734912 | G | C | 1 | a0005c0017t0014g0206 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.916-1457G>C | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47734912 | |||||||
| chr19:47734913 | C | A | 1 | a0005c0017t0014g0206 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.916-1456C>A | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47734913 | |||||||
| chr19:47734977 | C | T | 2 | a0001c0001t0001g0151 a0001c0001t0001g0152 |
2 | HG01943.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.916-1392C>T | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47734977 | |||||||
| chr19:47735017 | C | A | 236 | a0001c0001t0001g0019 a0001c0001t0001g0024 a0001c0001t0001g0028 others(233): Show |
240 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(237): Show |
intron_variant | MODIFIER | c.916-1352C>A | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47735017 | |||||||
| chr19:47735039 | G | A | 11 | a0001c0001t0010g0300 a0001c0001t0010g0344 a0001c0001t0010g0350 others(8): Show |
11 | HG01891.hp1 HG02055.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.916-1330G>A | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47735039 | |||||||
| chr19:47735146 | C | G | 1 | a0001c0002t0002g0247 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.916-1223C>G | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47735146 | |||||||
| chr19:47735156 | C | T | 9 | a0001c0001t0001g0199 a0001c0002t0004g0038 a0001c0002t0004g0064 others(6): Show |
9 | HG01891.hp1 HG02055.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.916-1213C>T | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47735156 | |||||||
| chr19:47735263 | G | A | 1 | a0001c0002t0003g0320 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.916-1106G>A | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47735263 | |||||||
| chr19:47735364 | G | A | 179 | a0001c0001t0001g0019 a0001c0001t0001g0024 a0001c0001t0001g0028 others(176): Show |
179 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.916-1005G>A | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47735364 | |||||||
| chr19:47735392 | A | G | 179 | a0001c0001t0001g0019 a0001c0001t0001g0024 a0001c0001t0001g0028 others(176): Show |
179 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.916-977A>G | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47735392 | |||||||
| chr19:47735574 | GGTGATAG others(8): Show |
G | 2 | a0001c0001t0001g0024 a0001c0001t0013g0072 |
2 | HG02723.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.916-794_916-780del others(15): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47735574 | |||||||
| chr19:47735598 | C | CA | 16 | a0001c0001t0001g0303 a0001c0002t0003g0004 a0001c0002t0003g0020 others(13): Show |
18 | HG02055.hp2 HG02258.hp2 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.916-761dupA | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 47735598 | ||||||
| chr19:47735719 | A | G | 1 | a0001c0012t0003g0006 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.916-650A>G | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47735719 | |||||||
| chr19:47735849 | C | T | 14 | a0001c0002t0004g0038 a0001c0002t0004g0059 a0001c0002t0004g0064 others(11): Show |
14 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.916-520C>T | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47735849 | |||||||
| chr19:47735904 | G | GA | 308 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0024 others(305): Show |
312 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(309): Show |
intron_variant | MODIFIER | c.916-454dupA | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 47735904 | ||||||
| chr19:47735928 | T | G | 1 | a0001c0002t0002g0036 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.916-441T>G | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47735928 | |||||||
| chr19:47735930 | G | C | 25 | a0001c0002t0002g0047 a0001c0002t0002g0054 a0001c0002t0002g0127 others(22): Show |
25 | HG00558.hp2 HG01361.hp1 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.916-439G>C | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47735930 | |||||||
| chr19:47735941 | T | C | 1 | a0001c0001t0001g0061 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.916-428T>C | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47735941 | |||||||
| chr19:47736177 | C | T | 5 | a0001c0001t0001g0368 a0002c0007t0007g0290 a0002c0007t0007g0291 others(2): Show |
5 | HG02129.hp2 HG02145.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.916-192C>T | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47736177 | |||||||
| chr19:47736178 | A | G | 219 | a0001c0001t0001g0019 a0001c0001t0001g0024 a0001c0001t0001g0028 others(216): Show |
223 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.916-191A>G | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47736178 | |||||||
| chr19:47736186 | A | G | 14 | a0001c0002t0004g0038 a0001c0002t0004g0059 a0001c0002t0004g0064 others(11): Show |
14 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.916-183A>G | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47736186 | |||||||
| chr19:47736300 | T | G | 179 | a0001c0001t0001g0019 a0001c0001t0001g0024 a0001c0001t0001g0028 others(176): Show |
179 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.916-69T>G | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47736300 | |||||||
| chr19:47736301 | G | A | 11 | a0001c0008t0005g0341 a0001c0008t0005g0363 a0001c0008t0005g0364 others(8): Show |
11 | HG00099.hp2 HG00280.hp1 HG00741.hp1 others(8): Show |
intron_variant | MODIFIER | c.916-68G>A | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47736301 | |||||||
| chr19:47736321 | C | G | 1 | a0001c0002t0004g0059 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.916-48C>G | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47736321 | |||||||
| chr19:47736344 | G | A | 1 | a0001c0005t0002g0370 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.916-25G>A | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47736344 | |||||||
| chr19:47736347 | G | A | 1 | a0001c0004t0007g0065 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.916-22G>A | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 4/5 | chr19 | 47736347 | |||||||
| chr19:47736556 | A | G | 14 | a0001c0002t0004g0038 a0001c0002t0004g0059 a0001c0002t0004g0064 others(11): Show |
14 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.1080+23A>G | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 5/5 | chr19 | 47736556 | |||||||
| chr19:47736711 | A | G | 1 | a0001c0002t0002g0069 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1080+178A>G | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 5/5 | chr19 | 47736711 | |||||||
| chr19:47736712 | A | G | 1 | a0001c0002t0002g0069 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1080+179A>G | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 5/5 | chr19 | 47736712 | |||||||
| chr19:47736813 | G | A | 2 | a0001c0002t0002g0007 a0001c0002t0002g0009 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1080+280G>A | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 5/5 | chr19 | 47736813 | |||||||
| chr19:47736905 | C | T | 3 | a0001c0001t0010g0300 a0001c0001t0010g0344 a0001c0001t0010g0350 |
3 | HG03195.hp2 HG03209.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1080+372C>T | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 5/5 | chr19 | 47736905 | |||||||
| chr19:47736959 | T | C | 5 | a0001c0001t0001g0199 a0001c0002t0002g0171 a0001c0002t0002g0319 others(2): Show |
5 | HG02572.hp2 HG02886.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.1080+426T>C | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 5/5 | chr19 | 47736959 | |||||||
| chr19:47736998 | G | C | 5 | a0001c0004t0006g0272 a0002c0007t0007g0290 a0002c0007t0007g0291 others(2): Show |
5 | HG02145.hp2 HG02922.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1080+465G>C | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 5/5 | chr19 | 47736998 | |||||||
| chr19:47737022 | C | G | 4 | a0001c0002t0002g0171 a0001c0002t0002g0319 a0001c0002t0004g0172 others(1): Show |
4 | HG02572.hp2 HG02886.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1080+489C>G | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 5/5 | chr19 | 47737022 | |||||||
| chr19:47737028 | A | G | 4 | a0001c0002t0002g0171 a0001c0002t0002g0319 a0001c0002t0004g0172 others(1): Show |
4 | HG02572.hp2 HG02886.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1080+495A>G | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 5/5 | chr19 | 47737028 | |||||||
| chr19:47737038 | T | C | 5 | a0001c0004t0006g0272 a0002c0007t0007g0290 a0002c0007t0007g0291 others(2): Show |
5 | HG02145.hp2 HG02922.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1080+505T>C | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 5/5 | chr19 | 47737038 | |||||||
| chr19:47737047 | C | T | 2 | a0001c0002t0002g0247 a0001c0002t0003g0292 |
2 | HG02615.hp1 NA18956.hp2 |
intron_variant | MODIFIER | c.1080+514C>T | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 5/5 | chr19 | 47737047 | |||||||
| chr19:47737179 | C | G | 2 | a0001c0002t0002g0042 a0001c0002t0002g0333 |
2 | HG02615.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1080+646C>G | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 5/5 | chr19 | 47737179 | |||||||
| chr19:47737180 | A | G | 1 | a0001c0001t0001g0337 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1080+647A>G | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 5/5 | chr19 | 47737180 | |||||||
| chr19:47737188 | G | A | 1 | a0001c0001t0001g0197 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1080+655G>A | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 5/5 | chr19 | 47737188 | |||||||
| chr19:47737219 | G | A | 1 | a0001c0010t0005g0015 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1080+686G>A | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 5/5 | chr19 | 47737219 | |||||||
| chr19:47737226 | C | T | 3 | a0001c0001t0001g0337 a0001c0002t0002g0233 a0001c0002t0002g0239 |
3 | HG02056.hp1 HG03041.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.1080+693C>T | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 5/5 | chr19 | 47737226 | |||||||
| chr19:47737228 | T | C | 17 | a0001c0002t0003g0027 a0001c0002t0003g0225 a0001c0002t0003g0288 others(14): Show |
19 | HG02486.hp1 HG02615.hp1 HG02622.hp1 others(16): Show |
intron_variant | MODIFIER | c.1080+695T>C | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 5/5 | chr19 | 47737228 | |||||||
| chr19:47737231 | C | CA | 20 | a0001c0001t0001g0024 a0001c0001t0001g0111 a0001c0001t0001g0266 others(17): Show |
20 | HG01192.hp1 HG01884.hp1 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.1080+715dupA | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr19 | 47737231 | ||||||
| chr19:47737231 | CA | C | 45 | a0001c0001t0001g0303 a0001c0001t0010g0300 a0001c0001t0010g0344 others(42): Show |
48 | HG00738.hp1 HG01243.hp2 HG01261.hp2 others(45): Show |
intron_variant | MODIFIER | c.1080+715delA | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr19 | 47737231 | ||||||
| chr19:47737279 | G | A | 10 | a0001c0002t0002g0245 a0001c0002t0002g0247 a0001c0005t0002g0105 others(7): Show |
10 | NA18612.hp2 NA18947.hp1 NA18949.hp1 others(7): Show |
intron_variant | MODIFIER | c.1080+746G>A | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 5/5 | chr19 | 47737279 | |||||||
| chr19:47737326 | G | C | 1 | a0001c0002t0002g0276 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1080+793G>C | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 5/5 | chr19 | 47737326 | |||||||
| chr19:47737422 | C | T | 1 | a0001c0001t0001g0123 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1080+889C>T | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 5/5 | chr19 | 47737422 | |||||||
| chr19:47737423 | A | G | 246 | a0001c0001t0001g0019 a0001c0001t0001g0024 a0001c0001t0001g0028 others(243): Show |
250 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(247): Show |
intron_variant | MODIFIER | c.1080+890A>G | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 5/5 | chr19 | 47737423 | |||||||
| chr19:47737532 | C | G | 1 | a0001c0002t0003g0292 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1080+999C>G | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 5/5 | chr19 | 47737532 | |||||||
| chr19:47737695 | A | C | 11 | a0001c0008t0005g0341 a0001c0008t0005g0363 a0001c0008t0005g0364 others(8): Show |
11 | HG00099.hp2 HG00280.hp1 HG00741.hp1 others(8): Show |
intron_variant | MODIFIER | c.1080+1162A>C | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 5/5 | chr19 | 47737695 | |||||||
| chr19:47737853 | C | T | 4 | a0002c0007t0007g0290 a0002c0007t0007g0291 a0002c0007t0007g0296 others(1): Show |
4 | HG02145.hp2 HG03041.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1080+1320C>T | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 5/5 | chr19 | 47737853 | |||||||
| chr19:47737876 | C | CT | 78 | a0001c0001t0001g0010 a0001c0001t0001g0056 a0001c0001t0001g0058 others(75): Show |
80 | HG00099.hp2 HG00280.hp1 HG00438.hp2 others(77): Show |
intron_variant | MODIFIER | c.1080+1365dupT | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr19 | 47737876 | ||||||
| chr19:47737876 | C | CTT | 10 | a0001c0001t0001g0238 a0001c0002t0004g0038 a0001c0002t0004g0064 others(7): Show |
10 | HG01346.hp2 HG01891.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.1080+1364_1080+136 others(6): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr19 | 47737876 | ||||||
| chr19:47737876 | CT | C | 6 | a0001c0001t0001g0062 a0001c0001t0001g0102 a0001c0001t0015g0091 others(3): Show |
6 | HG00735.hp1 HG01258.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.1080+1365delT | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr19 | 47737876 | ||||||
| chr19:47737954 | C | T | 1 | a0001c0001t0001g0303 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1080+1421C>T | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 5/5 | chr19 | 47737954 | |||||||
| chr19:47737973 | T | C | 224 | a0001c0001t0001g0019 a0001c0001t0001g0024 a0001c0001t0001g0028 others(221): Show |
226 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(223): Show |
intron_variant | MODIFIER | c.1080+1440T>C | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 5/5 | chr19 | 47737973 | |||||||
| chr19:47738449 | T | C | 1 | a0001c0003t0002g0039 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1080+1916T>C | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 5/5 | chr19 | 47738449 | |||||||
| chr19:47738548 | T | C | 179 | a0001c0001t0001g0019 a0001c0001t0001g0024 a0001c0001t0001g0028 others(176): Show |
179 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.1080+2015T>C | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 5/5 | chr19 | 47738548 | |||||||
| chr19:47738570 | G | C | 1 | a0001c0001t0001g0337 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1080+2037G>C | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 5/5 | chr19 | 47738570 | |||||||
| chr19:47738701 | T | G | 1 | a0001c0004t0019g0023 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1080+2168T>G | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 5/5 | chr19 | 47738701 | |||||||
| chr19:47738727 | C | T | 13 | a0001c0001t0001g0078 a0001c0001t0001g0083 a0001c0001t0001g0084 others(10): Show |
13 | HG00140.hp1 HG01081.hp1 HG01106.hp1 others(10): Show |
intron_variant | MODIFIER | c.1081-2154C>T | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 5/5 | chr19 | 47738727 | |||||||
| chr19:47738915 | T | C | 263 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0024 others(260): Show |
267 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.1081-1966T>C | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 5/5 | chr19 | 47738915 | |||||||
| chr19:47738921 | C | T | 7 | a0001c0002t0003g0301 a0001c0004t0003g0021 a0001c0004t0003g0022 others(4): Show |
7 | HG00738.hp1 HG02145.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1081-1960C>T | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 5/5 | chr19 | 47738921 | |||||||
| chr19:47738945 | G | A | 3 | a0001c0002t0002g0171 a0001c0002t0002g0319 a0001c0002t0009g0150 |
3 | HG02572.hp2 HG02886.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1081-1936G>A | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 5/5 | chr19 | 47738945 | |||||||
| chr19:47738952 | A | G | 3 | a0002c0007t0007g0291 a0002c0007t0007g0296 a0002c0007t0007g0342 |
3 | HG03041.hp2 HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1081-1929A>G | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 5/5 | chr19 | 47738952 | |||||||
| chr19:47739107 | T | C | 1 | a0001c0011t0001g0142 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1081-1774T>C | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 5/5 | chr19 | 47739107 | |||||||
| chr19:47739206 | G | C | 1 | a0001c0002t0002g0263 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1081-1675G>C | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 5/5 | chr19 | 47739206 | |||||||
| chr19:47739245 | C | T | 1 | a0001c0011t0001g0142 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1081-1636C>T | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 5/5 | chr19 | 47739245 | |||||||
| chr19:47739274 | A | AT | 11 | a0001c0002t0002g0140 a0001c0002t0002g0164 a0001c0002t0002g0188 others(8): Show |
11 | HG01175.hp2 HG01433.hp2 HG02027.hp1 others(8): Show |
intron_variant | MODIFIER | c.1081-1580dupT | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr19 | 47739274 | ||||||
| chr19:47739274 | A | ATTT | 10 | a0001c0002t0004g0038 a0001c0002t0004g0059 a0001c0002t0004g0064 others(7): Show |
10 | HG01884.hp2 HG01891.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.1081-1582_1081-158 others(7): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr19 | 47739274 | ||||||
| chr19:47739274 | AT | A | 16 | a0001c0002t0002g0040 a0001c0002t0002g0051 a0001c0002t0002g0120 others(13): Show |
17 | HG01167.hp1 HG01243.hp2 HG02015.hp1 others(14): Show |
intron_variant | MODIFIER | c.1081-1580delT | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr19 | 47739274 | ||||||
| chr19:47739274 | ATTT | A | 35 | a0001c0001t0001g0050 a0001c0001t0001g0066 a0001c0001t0001g0110 others(32): Show |
36 | HG00099.hp2 HG00280.hp1 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.1081-1582_1081-158 others(7): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr19 | 47739274 | ||||||
| chr19:47739274 | ATTTT | A | 137 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0024 others(134): Show |
137 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.1081-1583_1081-158 others(8): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr19 | 47739274 | ||||||
| chr19:47739274 | ATTTTT | A | 29 | a0001c0001t0001g0046 a0001c0001t0001g0056 a0001c0001t0001g0057 others(26): Show |
30 | HG00438.hp2 HG00735.hp2 HG01069.hp2 others(27): Show |
intron_variant | MODIFIER | c.1081-1584_1081-158 others(9): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr19 | 47739274 | ||||||
| chr19:47739274 | ATTTTTTT others(3): Show |
A | 25 | a0001c0001t0001g0028 a0001c0002t0003g0004 a0001c0002t0003g0020 others(22): Show |
26 | HG00738.hp1 HG01516.hp2 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.1081-1589_1081-158 others(14): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr19 | 47739274 | ||||||
| chr19:47739274 | ATTTTTTT others(4): Show |
A | 2 | a0001c0002t0003g0306 a0002c0007t0007g0291 |
2 | HG02965.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1081-1590_1081-158 others(15): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr19 | 47739274 | ||||||
| chr19:47739351 | A | G | 2 | a0001c0015t0001g0104 a0002c0009t0001g0132 |
2 | HG04204.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1081-1530A>G | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 5/5 | chr19 | 47739351 | |||||||
| chr19:47739366 | C | T | 3 | a0001c0015t0001g0104 a0001c0024t0001g0329 a0002c0009t0001g0132 |
3 | HG04204.hp1 NA19000.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1081-1515C>T | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 5/5 | chr19 | 47739366 | |||||||
| chr19:47739474 | G | A | 1 | a0001c0001t0001g0255 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1081-1407G>A | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 5/5 | chr19 | 47739474 | |||||||
| chr19:47739532 | C | T | 8 | a0001c0002t0006g0003 a0001c0002t0006g0026 a0001c0002t0006g0033 others(5): Show |
9 | HG01243.hp2 HG02109.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.1081-1349C>T | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 5/5 | chr19 | 47739532 | |||||||
| chr19:47739542 | G | A | 11 | a0001c0008t0005g0341 a0001c0008t0005g0363 a0001c0008t0005g0364 others(8): Show |
11 | HG00099.hp2 HG00280.hp1 HG00741.hp1 others(8): Show |
intron_variant | MODIFIER | c.1081-1339G>A | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 5/5 | chr19 | 47739542 | |||||||
| chr19:47739587 | C | T | 1 | a0001c0002t0004g0148 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1081-1294C>T | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 5/5 | chr19 | 47739587 | |||||||
| chr19:47739597 | C | CA | 41 | a0001c0001t0001g0056 a0001c0001t0001g0074 a0001c0001t0001g0106 others(38): Show |
41 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(38): Show |
intron_variant | MODIFIER | c.1081-1265dupA | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr19 | 47739597 | ||||||
| chr19:47739597 | CA | C | 41 | a0001c0001t0001g0169 a0001c0002t0002g0007 a0001c0002t0002g0200 others(38): Show |
43 | HG00738.hp1 HG01891.hp1 HG01891.hp2 others(40): Show |
intron_variant | MODIFIER | c.1081-1265delA | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr19 | 47739597 | ||||||
| chr19:47739640 | G | A | 1 | a0001c0002t0002g0120 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1081-1241G>A | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 5/5 | chr19 | 47739640 | |||||||
| chr19:47739779 | A | G | 47 | a0001c0001t0001g0010 a0001c0001t0001g0046 a0001c0001t0001g0055 others(44): Show |
47 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(44): Show |
intron_variant | MODIFIER | c.1081-1102A>G | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 5/5 | chr19 | 47739779 | |||||||
| chr19:47740122 | T | G | 2 | a0001c0015t0001g0104 a0002c0009t0001g0132 |
2 | HG04204.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1081-759T>G | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 5/5 | chr19 | 47740122 | |||||||
| chr19:47740207 | AATTTTTA others(31): Show |
A | 1 | a0001c0002t0006g0026 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1081-672_1081-635d others(40): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr19 | 47740207 | ||||||
| chr19:47740218 | C | T | 1 | a0001c0001t0001g0337 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1081-663C>T | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 5/5 | chr19 | 47740218 | |||||||
| chr19:47740252 | A | G | 270 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0024 others(267): Show |
274 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(271): Show |
intron_variant | MODIFIER | c.1081-629A>G | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 5/5 | chr19 | 47740252 | |||||||
| chr19:47740385 | G | A | 1 | a0001c0003t0002g0008 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1081-496G>A | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 5/5 | chr19 | 47740385 | |||||||
| chr19:47740430 | C | G | 1 | a0002c0007t0003g0032 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1081-451C>G | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 5/5 | chr19 | 47740430 | |||||||
| chr19:47740436 | C | CA | 24 | a0001c0001t0001g0066 a0001c0002t0002g0250 a0001c0002t0003g0004 others(21): Show |
25 | HG00738.hp1 HG01891.hp2 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.1081-436dupA | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr19 | 47740436 | ||||||
| chr19:47740441 | A | AC | 7 | a0001c0002t0003g0175 a0001c0002t0003g0176 a0001c0002t0003g0178 others(4): Show |
7 | HG01069.hp1 HG01928.hp2 HG01993.hp1 others(4): Show |
intron_variant | MODIFIER | c.1081-440_1081-439i others(3): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 5/5 | chr19 | 47740441 | |||||||
| chr19:47740441 | A | C | 1 | a0001c0002t0002g0143 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1081-440A>C | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 5/5 | chr19 | 47740441 | |||||||
| chr19:47740446 | C | A | 1 | a0001c0001t0001g0055 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1081-435C>A | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 5/5 | chr19 | 47740446 | |||||||
| chr19:47740469 | G | C | 3 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0001g0389 |
3 | NA18954.hp1 NA18960.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.1081-412G>C | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 5/5 | chr19 | 47740469 | |||||||
| chr19:47740543 | C | T | 1 | a0001c0002t0017g0298 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1081-338C>T | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 5/5 | chr19 | 47740543 | |||||||
| chr19:47740560 | A | G | 1 | a0001c0001t0001g0073 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1081-321A>G | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 5/5 | chr19 | 47740560 | |||||||
| chr19:47740663 | T | C | 2 | a0001c0001t0001g0083 a0001c0001t0001g0311 |
2 | HG00140.hp1 HG00639.hp1 |
intron_variant | MODIFIER | c.1081-218T>C | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 5/5 | chr19 | 47740663 | |||||||
| chr19:47740788 | C | CT | 197 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0024 others(194): Show |
197 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(194): Show |
intron_variant | MODIFIER | c.1081-93_1081-92ins others(1): Show |
EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 5/5 | chr19 | 47740788 | |||||||
| chr19:47740876 | C | G | 1 | a0001c0004t0002g0237 | 1 | HG02056.hp2 | splice_region_variant&intron_variant | LOW | c.1081-5C>G | EHD2 | ENSG00000024422.12 | transcript | ENST00000263277.8 | protein_coding | 5/5 | chr19 | 47740876 |