Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 54505 |
| ensemblid | ENSG00000067248.11 |
| hgncid | 15815 |
| symbol | DHX29 |
| name | DExH-box helicase 29 |
| refseq_nuc | NM_019030.4 |
| refseq_prot | NP_061903.2 |
| ensembl_nuc | ENST00000251636.10 |
| ensembl_prot | ENSP00000251636.5 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 55256055 |
| end | 55307694 |
| strand | - |
| ver | v1.2 |
| region | chr5:55256055-55307694 |
| region5000 | chr5:55251055-55312694 |
| regionname0 | DHX29_chr5_55256055_55307694 |
| regionname5000 | DHX29_chr5_55251055_55312694 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1369 | 330 | 85 | 52 | 152 | 11 | 28 | 124 | DHX29_chr5_55251055_55312694 | DHX29 | MGGKN others(1364): Show |
chr5 | 55251055 | 55312694 |
| a0002 | 0/0 | 1369 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | MGGKN others(1364): Show |
chr5 | 55251055 | 55312694 |
| a0003 | 0/0 | 1369 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | MGGKN others(1364): Show |
chr5 | 55251055 | 55312694 |
| a0004 | 0/0 | 1369 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | MGGKN others(1364): Show |
chr5 | 55251055 | 55312694 |
| a0005 | 0/0 | 1369 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | MGGKN others(1364): Show |
chr5 | 55251055 | 55312694 |
| a0006 | 0/0 | 1369 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | MGGKN others(1364): Show |
chr5 | 55251055 | 55312694 |
| a0007 | 0/0 | 1369 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | MGGKN others(1364): Show |
chr5 | 55251055 | 55312694 |
| a0008 | 0/0 | 1369 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | DHX29_chr5_55251055_55312694 | DHX29 | MGGKN others(1364): Show |
chr5 | 55251055 | 55312694 |
| a0009 | 0/0 | 324 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | DHX29_chr5_55251055_55312694 | DHX29 | MGGKN others(319): Show |
chr5 | 55251055 | 55312694 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 4107 | 240 | 59 | 43 | 103 | 9 | 24 | DHX29_chr5_55251055_55312694 | DHX29 | ATGGG others(4102): Show |
chr5 | 55251055 | 55312694 | ||
| a0001c0002 | 0/0 | 4107 | 80 | 24 | 5 | 45 | 2 | 4 | DHX29_chr5_55251055_55312694 | DHX29 | ATGGG others(4102): Show |
chr5 | 55251055 | 55312694 | ||
| a0001c0003 | 0/0 | 4107 | 3 | 0 | 3 | 0 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | ATGGG others(4102): Show |
chr5 | 55251055 | 55312694 | ||
| a0001c0006 | 0/0 | 4107 | 1 | 1 | 0 | 0 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | ATGGG others(4102): Show |
chr5 | 55251055 | 55312694 | ||
| a0001c0007 | 0/0 | 4107 | 1 | 1 | 0 | 0 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | ATGGG others(4102): Show |
chr5 | 55251055 | 55312694 | ||
| a0001c0009 | 0/0 | 4107 | 1 | 0 | 1 | 0 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | ATGGG others(4102): Show |
chr5 | 55251055 | 55312694 | ||
| a0001c0012 | 0/0 | 4107 | 1 | 0 | 0 | 1 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | ATGGG others(4102): Show |
chr5 | 55251055 | 55312694 | ||
| a0001c0013 | 0/0 | 4107 | 1 | 0 | 0 | 1 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | ATGGG others(4102): Show |
chr5 | 55251055 | 55312694 | ||
| a0001c0014 | 0/0 | 4107 | 1 | 0 | 0 | 1 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | ATGGG others(4102): Show |
chr5 | 55251055 | 55312694 | ||
| a0001c0015 | 0/0 | 4107 | 1 | 0 | 0 | 1 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | ATGGG others(4102): Show |
chr5 | 55251055 | 55312694 | ||
| a0002c0004 | 0/0 | 4107 | 2 | 1 | 1 | 0 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | ATGGG others(4102): Show |
chr5 | 55251055 | 55312694 | ||
| a0003c0005 | 0/0 | 4107 | 2 | 2 | 0 | 0 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | ATGGG others(4102): Show |
chr5 | 55251055 | 55312694 | ||
| a0004c0017 | 0/0 | 4107 | 1 | 0 | 0 | 0 | 1 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | ATGGG others(4102): Show |
chr5 | 55251055 | 55312694 | ||
| a0005c0018 | 0/0 | 4107 | 1 | 0 | 1 | 0 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | ATGGG others(4102): Show |
chr5 | 55251055 | 55312694 | ||
| a0006c0011 | 0/0 | 4107 | 1 | 0 | 0 | 0 | 0 | 1 | DHX29_chr5_55251055_55312694 | DHX29 | ATGGG others(4102): Show |
chr5 | 55251055 | 55312694 | ||
| a0007c0010 | 0/0 | 4107 | 1 | 0 | 0 | 0 | 0 | 1 | DHX29_chr5_55251055_55312694 | DHX29 | ATGGG others(4102): Show |
chr5 | 55251055 | 55312694 | ||
| a0008c0008 | 0/0 | 4107 | 1 | 0 | 0 | 1 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | ATGGG others(4102): Show |
chr5 | 55251055 | 55312694 | ||
| a0009c0016 | 0/0 | 4122 | 1 | 0 | 0 | 1 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | ATGGG others(4117): Show |
chr5 | 55251055 | 55312694 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 4664 | 198 | 44 | 38 | 84 | 9 | 21 | DHX29_chr5_55251055_55312694 | DHX29 | GAGAA others(4659): Show |
chr5 | 55251055 | 55312694 |
| a0001c0001t0002 | 0/0 | 4664 | 39 | 15 | 4 | 17 | 0 | 3 | DHX29_chr5_55251055_55312694 | DHX29 | GAGAA others(4659): Show |
chr5 | 55251055 | 55312694 |
| a0001c0001t0003 | 0/0 | 4664 | 2 | 0 | 0 | 2 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | GAGAA others(4659): Show |
chr5 | 55251055 | 55312694 |
| a0001c0001t0005 | 0/0 | 4664 | 1 | 0 | 1 | 0 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | GAGAA others(4659): Show |
chr5 | 55251055 | 55312694 |
| a0001c0002t0001 | 0/0 | 4664 | 80 | 24 | 5 | 45 | 2 | 4 | DHX29_chr5_55251055_55312694 | DHX29 | GAGAA others(4659): Show |
chr5 | 55251055 | 55312694 |
| a0001c0003t0001 | 0/0 | 4664 | 3 | 0 | 3 | 0 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | GAGAA others(4659): Show |
chr5 | 55251055 | 55312694 |
| a0001c0006t0001 | 0/0 | 4664 | 1 | 1 | 0 | 0 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | GAGAA others(4659): Show |
chr5 | 55251055 | 55312694 |
| a0001c0007t0001 | 0/0 | 4664 | 1 | 1 | 0 | 0 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | GAGAA others(4659): Show |
chr5 | 55251055 | 55312694 |
| a0001c0009t0001 | 0/0 | 4664 | 1 | 0 | 1 | 0 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | GAGAA others(4659): Show |
chr5 | 55251055 | 55312694 |
| a0001c0012t0002 | 0/0 | 4664 | 1 | 0 | 0 | 1 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | GAGAA others(4659): Show |
chr5 | 55251055 | 55312694 |
| a0001c0013t0001 | 0/0 | 4664 | 1 | 0 | 0 | 1 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | GAGAA others(4659): Show |
chr5 | 55251055 | 55312694 |
| a0001c0014t0001 | 0/0 | 4664 | 1 | 0 | 0 | 1 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | GAGAA others(4659): Show |
chr5 | 55251055 | 55312694 |
| a0001c0015t0001 | 0/0 | 4664 | 1 | 0 | 0 | 1 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | GAGAA others(4659): Show |
chr5 | 55251055 | 55312694 |
| a0002c0004t0004 | 0/0 | 4664 | 2 | 1 | 1 | 0 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | GAGAA others(4659): Show |
chr5 | 55251055 | 55312694 |
| a0003c0005t0001 | 0/0 | 4664 | 2 | 2 | 0 | 0 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | GAGAA others(4659): Show |
chr5 | 55251055 | 55312694 |
| a0004c0017t0001 | 0/0 | 4664 | 1 | 0 | 0 | 0 | 1 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | GAGAA others(4659): Show |
chr5 | 55251055 | 55312694 |
| a0005c0018t0002 | 0/0 | 4664 | 1 | 0 | 1 | 0 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | GAGAA others(4659): Show |
chr5 | 55251055 | 55312694 |
| a0006c0011t0001 | 0/0 | 4664 | 1 | 0 | 0 | 0 | 0 | 1 | DHX29_chr5_55251055_55312694 | DHX29 | GAGAA others(4659): Show |
chr5 | 55251055 | 55312694 |
| a0007c0010t0001 | 0/0 | 4664 | 1 | 0 | 0 | 0 | 0 | 1 | DHX29_chr5_55251055_55312694 | DHX29 | GAGAA others(4659): Show |
chr5 | 55251055 | 55312694 |
| a0008c0008t0001 | 0/0 | 4664 | 1 | 0 | 0 | 1 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | GAGAA others(4659): Show |
chr5 | 55251055 | 55312694 |
| a0009c0016t0001 | 0/0 | 4679 | 1 | 0 | 0 | 1 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | GAGAA others(4674): Show |
chr5 | 55251055 | 55312694 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 22 | 3 | 2 | 15 | 1 | 1 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0003 | 0/0 | 5 | 3 | 1 | 0 | 1 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0005 | 0/0 | 4 | 0 | 0 | 0 | 0 | 4 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0008 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0009 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0025 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0026 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0085 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0086 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0002g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0002g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0002g0011 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0002g0012 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0002g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0002g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0002g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0002g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0002g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0002g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0002g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0002g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0002g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0003g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0003g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0001t0005g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0002t0001g0002 | 0/0 | 7 | 0 | 1 | 5 | 1 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0002t0001g0004 | 0/0 | 5 | 0 | 0 | 4 | 0 | 1 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0002t0001g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0002t0001g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0002t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0002t0001g0031 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0002t0001g0032 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0002t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0002t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0002t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0002t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0002t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0002t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0002t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0002t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0002t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0002t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0002t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0002t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0002t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0002t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0002t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0002t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0002t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0002t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0002t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0002t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0002t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0002t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0002t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0002t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0002t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0002t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0002t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0003t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0003t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0003t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0006t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0007t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0009t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0012t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0013t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0014t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0001c0015t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0002c0004t0004g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0002c0004t0004g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0003c0005t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0003c0005t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0004c0017t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0005c0018t0002g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0006c0011t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0007c0010t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0008c0008t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| a0009c0016t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0026 | EUR | GBR | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG00140 | hp2 | a0004 | c0017 | t0001 | g0112 | EUR | GBR | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | CHS | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG00423 | hp2 | a0001 | c0002 | t0001 | g0227 | EAS | CHS | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | CHS | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | CHS | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | CHS | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | CHS | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG00621 | hp2 | a0001 | c0002 | t0001 | g0221 | EAS | CHS | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG00642 | hp2 | a0001 | c0003 | t0001 | g0114 | AMR | PUR | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | PUR | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG00733 | hp2 | a0001 | c0002 | t0001 | g0031 | AMR | PUR | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG00735 | hp1 | a0001 | c0002 | t0001 | g0239 | AMR | PUR | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG00735 | hp2 | a0001 | c0009 | t0001 | g0121 | AMR | PUR | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0012 | AMR | PUR | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0095 | AMR | PUR | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG01074 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | PUR | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | PUR | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG01167 | hp1 | a0001 | c0002 | t0001 | g0249 | AMR | PUR | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG01167 | hp2 | a0001 | c0003 | t0001 | g0092 | AMR | PUR | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG01168 | hp2 | a0002 | c0004 | t0004 | g0042 | AMR | PUR | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0051 | AMR | PUR | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | CLM | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG01256 | hp1 | a0001 | c0002 | t0001 | g0213 | AMR | CLM | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | CLM | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG01258 | hp1 | a0001 | c0003 | t0001 | g0071 | AMR | CLM | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | CLM | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG01346 | hp1 | a0001 | c0001 | t0005 | g0263 | AMR | CLM | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | CLM | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | CLM | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | CLM | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0012 | AMR | CLM | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | CLM | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0094 | EUR | IBS | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0116 | EUR | IBS | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG01516 | hp2 | a0001 | c0002 | t0001 | g0002 | EUR | IBS | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG01517 | hp1 | a0001 | c0002 | t0001 | g0032 | EUR | IBS | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | ACB | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0029 | AFR | ACB | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | PEL | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | PEL | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | PEL | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0203 | AMR | PEL | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | PEL | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG01993 | hp1 | a0005 | c0018 | t0002 | g0206 | AMR | PEL | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | PEL | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | KHV | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | KHV | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | ACB | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | ACB | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG02056 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | KHV | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | KHV | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG02074 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | KHV | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | KHV | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG02080 | hp2 | a0001 | c0002 | t0001 | g0223 | EAS | KHV | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | KHV | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | KHV | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG02132 | hp1 | a0001 | c0002 | t0001 | g0032 | EAS | KHV | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | KHV | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | ACB | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG02145 | hp2 | a0001 | c0007 | t0001 | g0256 | AFR | ACB | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG02155 | hp2 | a0001 | c0002 | t0001 | g0225 | EAS | CDX | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0029 | AFR | ACB | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | ACB | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0192 | AFR | ACB | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | ACB | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0012 | AMR | PEL | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG02280 | hp1 | a0001 | c0002 | t0001 | g0252 | AFR | ACB | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0010 | AFR | ACB | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG02451 | hp1 | a0001 | c0002 | t0001 | g0033 | AFR | ACB | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | KHV | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | KHV | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | GWD | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | GWD | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0109 | SAS | PJL | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0079 | SAS | PJL | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | GWD | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG02615 | hp2 | a0001 | c0002 | t0001 | g0039 | AFR | GWD | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | GWD | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG02622 | hp2 | a0001 | c0006 | t0001 | g0036 | AFR | GWD | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0194 | AFR | GWD | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG02630 | hp2 | a0001 | c0002 | t0001 | g0030 | AFR | GWD | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | GWD | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0159 | SAS | PJL | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0115 | SAS | PJL | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0083 | SAS | PJL | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0191 | AFR | GWD | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG02717 | hp2 | a0002 | c0004 | t0004 | g0043 | AFR | GWD | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG02735 | hp2 | a0001 | c0002 | t0001 | g0251 | SAS | PJL | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0098 | SAS | PJL | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0073 | SAS | PJL | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0028 | AFR | GWD | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG02809 | hp2 | a0001 | c0002 | t0001 | g0243 | AFR | GWD | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | GWD | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0027 | AFR | GWD | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG02886 | hp1 | a0001 | c0002 | t0001 | g0255 | AFR | GWD | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | GWD | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG02895 | hp1 | a0001 | c0002 | t0001 | g0244 | AFR | GWD | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG02895 | hp2 | a0001 | c0002 | t0001 | g0041 | AFR | GWD | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0187 | AFR | GWD | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | GWD | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG02897 | hp1 | a0001 | c0002 | t0001 | g0247 | AFR | GWD | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0027 | AFR | GWD | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG02922 | hp1 | a0001 | c0002 | t0001 | g0242 | AFR | ESN | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG02922 | hp2 | a0001 | c0002 | t0001 | g0257 | AFR | ESN | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0165 | AFR | ESN | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | ESN | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | ESN | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG02976 | hp2 | a0001 | c0002 | t0001 | g0241 | AFR | ESN | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0169 | SAS | PJL | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | GWD | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | GWD | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG03098 | hp1 | a0001 | c0002 | t0001 | g0254 | AFR | MSL | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0188 | AFR | MSL | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | ESN | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG03130 | hp2 | a0003 | c0005 | t0001 | g0054 | AFR | ESN | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG03195 | hp1 | a0001 | c0002 | t0001 | g0033 | AFR | ESN | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | ESN | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG03209 | hp1 | a0001 | c0002 | t0001 | g0240 | AFR | MSL | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | MSL | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG03225 | hp1 | a0001 | c0002 | t0001 | g0030 | AFR | MSL | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | MSL | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG03453 | hp1 | a0001 | c0002 | t0001 | g0246 | AFR | MSL | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | MSL | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | MSL | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | MSL | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0047 | SAS | PJL | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0167 | SAS | PJL | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0193 | AFR | ESN | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | GWD | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0182 | AFR | MSL | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0010 | AFR | MSL | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG03654 | hp1 | a0006 | c0011 | t0001 | g0101 | SAS | PJL | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG03654 | hp2 | a0007 | c0010 | t0001 | g0184 | SAS | PJL | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0011 | SAS | PJL | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG03704 | hp2 | a0001 | c0002 | t0001 | g0004 | SAS | PJL | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG03927 | hp1 | a0001 | c0002 | t0001 | g0220 | SAS | BEB | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0166 | SAS | BEB | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0190 | SAS | BEB | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0058 | SAS | BEB | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0163 | SAS | STU | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0186 | SAS | STU | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0202 | SAS | STU | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | STU | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA18522 | hp1 | a0003 | c0005 | t0001 | g0055 | AFR | YRI | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | YRI | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0189 | EAS | CHB | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | CHB | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | CHB | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA18747 | hp2 | a0001 | c0002 | t0001 | g0007 | EAS | CHB | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA18906 | hp1 | a0001 | c0002 | t0001 | g0258 | AFR | YRI | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA18906 | hp2 | a0001 | c0002 | t0001 | g0037 | AFR | YRI | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA18944 | hp1 | a0001 | c0002 | t0001 | g0216 | EAS | JPT | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA18946 | hp1 | a0001 | c0002 | t0001 | g0214 | EAS | JPT | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA18947 | hp2 | a0001 | c0002 | t0001 | g0228 | EAS | JPT | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA18948 | hp2 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA18949 | hp1 | a0001 | c0002 | t0001 | g0031 | EAS | JPT | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA18950 | hp1 | a0001 | c0001 | t0003 | g0034 | EAS | JPT | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0197 | EAS | JPT | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA18957 | hp1 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA18960 | hp2 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA18962 | hp1 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA18966 | hp2 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA18967 | hp2 | a0001 | c0015 | t0001 | g0141 | EAS | JPT | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA18968 | hp2 | a0001 | c0002 | t0001 | g0236 | EAS | JPT | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA18971 | hp2 | a0001 | c0002 | t0001 | g0226 | EAS | JPT | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA18972 | hp1 | a0001 | c0012 | t0002 | g0201 | EAS | JPT | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA18975 | hp2 | a0001 | c0002 | t0001 | g0212 | EAS | JPT | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA18977 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA18979 | hp1 | a0001 | c0002 | t0001 | g0215 | EAS | JPT | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA18979 | hp2 | a0008 | c0008 | t0001 | g0078 | EAS | JPT | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA18980 | hp2 | a0001 | c0002 | t0001 | g0232 | EAS | JPT | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0196 | EAS | JPT | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA18984 | hp1 | a0001 | c0002 | t0001 | g0222 | EAS | JPT | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA18984 | hp2 | a0001 | c0014 | t0001 | g0099 | EAS | JPT | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA18985 | hp2 | a0001 | c0002 | t0001 | g0217 | EAS | JPT | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA18987 | hp1 | a0001 | c0002 | t0001 | g0237 | EAS | JPT | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA18988 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA18991 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA18993 | hp2 | a0001 | c0013 | t0001 | g0231 | EAS | JPT | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA18997 | hp1 | a0001 | c0002 | t0001 | g0218 | EAS | JPT | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA18997 | hp2 | a0009 | c0016 | t0001 | g0259 | EAS | JPT | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA19000 | hp1 | a0001 | c0002 | t0001 | g0230 | EAS | JPT | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA19000 | hp2 | a0001 | c0002 | t0001 | g0219 | EAS | JPT | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA19002 | hp1 | a0001 | c0002 | t0001 | g0211 | EAS | JPT | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA19005 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA19006 | hp1 | a0001 | c0002 | t0001 | g0209 | EAS | JPT | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA19009 | hp1 | a0001 | c0002 | t0001 | g0224 | EAS | JPT | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA19011 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | LWK | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA19030 | hp2 | a0001 | c0002 | t0001 | g0253 | AFR | LWK | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA19056 | hp2 | a0001 | c0002 | t0001 | g0234 | EAS | JPT | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA19060 | hp1 | a0001 | c0002 | t0001 | g0229 | EAS | JPT | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA19063 | hp1 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0198 | EAS | JPT | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA19067 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA19074 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA19075 | hp1 | a0001 | c0002 | t0001 | g0235 | EAS | JPT | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0200 | EAS | JPT | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA19081 | hp2 | a0001 | c0001 | t0003 | g0035 | EAS | JPT | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA19082 | hp1 | a0001 | c0002 | t0001 | g0238 | EAS | JPT | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0195 | EAS | JPT | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA19083 | hp2 | a0001 | c0001 | t0002 | g0204 | EAS | JPT | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA19087 | hp1 | a0001 | c0002 | t0001 | g0245 | EAS | JPT | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA19091 | hp1 | a0001 | c0002 | t0001 | g0233 | EAS | JPT | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | YRI | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA19240 | hp2 | a0001 | c0002 | t0001 | g0210 | AFR | YRI | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | ASW | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | ASW | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0144 | EUR | TSI | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0173 | EUR | TSI | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0024 | EUR | TSI | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0072 | EUR | TSI | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0076 | SAS | GIH | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA20905 | hp2 | a0001 | c0002 | t0001 | g0250 | SAS | GIH | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0176 | AMR | CLM | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0061 | AMR | CLM | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | ACB | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG02109 | hp2 | a0001 | c0002 | t0001 | g0038 | AFR | ACB | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG02486 | hp1 | a0001 | c0002 | t0001 | g0040 | AFR | ACB | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | ACB | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG02559 | hp2 | a0001 | c0002 | t0001 | g0248 | AFR | ACB | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | MSL | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0028 | AFR | MSL | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | USA | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | USA | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | LWK | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0010 | AFR | LWK | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0085 | REF | REF | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0086 | REF | REF | DHX29_chr5_55251055_55312694 | DHX29 | chr5 | 55251055 | 55312694 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:55262682 | G | A | 1 | a0007 | 1 | HG03654.hp2 | missense_variant | MODERATE | c.3776C>T | p.Ser1259Phe | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 24/27 | 3897/4664 | 3776/4110 | 1259/1369 | chr5 | 55262682 | |||
| chr5:55267708 | T | C | 1 | a0006 | 1 | HG03654.hp1 | missense_variant | MODERATE | c.3409A>G | p.Thr1137Ala | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 22/27 | 3530/4664 | 3409/4110 | 1137/1369 | chr5 | 55267708 | |||
| chr5:55283439 | G | A | 1 | a0003 | 2 | HG03130.hp2 NA18522.hp1 |
missense_variant | MODERATE | c.1729C>T | p.His577Tyr | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 11/27 | 1850/4664 | 1729/4110 | 577/1369 | chr5 | 55283439 | |||
| chr5:55283723 | A | G | 1 | a0008 | 1 | NA18979.hp2 | missense_variant | MODERATE | c.1445T>C | p.Met482Thr | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 11/27 | 1566/4664 | 1445/4110 | 482/1369 | chr5 | 55283723 | |||
| chr5:55289350 | G | A | 1 | a0009 | 1 | NA18997.hp2 | missense_variant | MODERATE | c.986C>T | p.Pro329Leu | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 8/27 | 1107/4664 | 986/4110 | 329/1369 | chr5 | 55289350 | |||
| chr5:55289354 | T | G | 1 | a0009 | 1 | NA18997.hp2 | missense_variant | MODERATE | c.982A>C | p.Lys328Gln | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 8/27 | 1103/4664 | 982/4110 | 328/1369 | chr5 | 55289354 | |||
| chr5:55289357 | T | A | 1 | a0009 | 1 | NA18997.hp2 | stop_gained | HIGH | c.979A>T | p.Lys327* | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 8/27 | 1100/4664 | 979/4110 | 327/1369 | chr5 | 55289357 | |||
| chr5:55289358 | C | CTGAAGAA others(8): Show |
1 | a0009 | 1 | NA18997.hp2 | disruptive_inframe_insertion | MODERATE | c.977_978insCCTTTCTC others(7): Show |
p.Arg326delinsSerLeu others(12): Show |
DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 8/27 | 1098/4664 | 977/4110 | 326/1369 | chr5 | 55289358 | |||
| chr5:55289362 | T | C | 1 | a0009 | 1 | NA18997.hp2 | missense_variant | MODERATE | c.974A>G | p.Glu325Gly | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 8/27 | 1095/4664 | 974/4110 | 325/1369 | chr5 | 55289362 | |||
| chr5:55289363 | C | A | 1 | a0009 | 1 | NA18997.hp2 | stop_gained | HIGH | c.973G>T | p.Glu325* | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 8/27 | 1094/4664 | 973/4110 | 325/1369 | chr5 | 55289363 | |||
| chr5:55289365 | T | A | 1 | a0009 | 1 | NA18997.hp2 | missense_variant | MODERATE | c.971A>T | p.Asn324Ile | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 8/27 | 1092/4664 | 971/4110 | 324/1369 | chr5 | 55289365 | |||
| chr5:55289383 | T | G | 1 | a0009 | 1 | NA18997.hp2 | missense_variant | MODERATE | c.953A>C | p.Lys318Thr | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 8/27 | 1074/4664 | 953/4110 | 318/1369 | chr5 | 55289383 | |||
| chr5:55289385 | C | T | 1 | a0002 | 2 | HG01168.hp2 HG02717.hp2 |
missense_variant | MODERATE | c.951G>A | p.Met317Ile | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 8/27 | 1072/4664 | 951/4110 | 317/1369 | chr5 | 55289385 | |||
| chr5:55289387 | T | G | 1 | a0009 | 1 | NA18997.hp2 | missense_variant | MODERATE | c.949A>C | p.Met317Leu | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 8/27 | 1070/4664 | 949/4110 | 317/1369 | chr5 | 55289387 | |||
| chr5:55289397 | A | T | 1 | a0009 | 1 | NA18997.hp2 | missense_variant | MODERATE | c.939T>A | p.Phe313Leu | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 8/27 | 1060/4664 | 939/4110 | 313/1369 | chr5 | 55289397 | |||
| chr5:55289401 | A | T | 1 | a0009 | 1 | NA18997.hp2 | missense_variant | MODERATE | c.935T>A | p.Val312Glu | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 8/27 | 1056/4664 | 935/4110 | 312/1369 | chr5 | 55289401 | |||
| chr5:55289405 | G | T | 1 | a0009 | 1 | NA18997.hp2 | missense_variant | MODERATE | c.931C>A | p.Pro311Thr | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 8/27 | 1052/4664 | 931/4110 | 311/1369 | chr5 | 55289405 | |||
| chr5:55289410 | T | A | 1 | a0009 | 1 | NA18997.hp2 | missense_variant | MODERATE | c.926A>T | p.Asp309Val | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 8/27 | 1047/4664 | 926/4110 | 309/1369 | chr5 | 55289410 | |||
| chr5:55289420 | T | C | 1 | a0001 | 2 | HG02129.hp2 NA18957.hp2 |
missense_variant | MODERATE | c.916A>G | p.Thr306Ala | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 8/27 | 1037/4664 | 916/4110 | 306/1369 | chr5 | 55289420 | |||
| chr5:55289423 | C | T | 1 | a0009 | 1 | NA18997.hp2 | missense_variant | MODERATE | c.913G>A | p.Glu305Lys | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 8/27 | 1034/4664 | 913/4110 | 305/1369 | chr5 | 55289423 | |||
| chr5:55289427 | T | G | 1 | a0009 | 1 | NA18997.hp2 | missense_variant&splice_region_variant | MODERATE | c.909A>C | p.Glu303Asp | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 8/27 | 1030/4664 | 909/4110 | 303/1369 | chr5 | 55289427 | |||
| chr5:55297373 | T | G | 1 | a0004 | 1 | HG00140.hp2 | missense_variant | MODERATE | c.287A>C | p.Gln96Pro | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 3/27 | 408/4664 | 287/4110 | 96/1369 | chr5 | 55297373 | |||
| chr5:55297382 | T | G | 1 | a0005 | 1 | HG01993.hp1 | missense_variant | MODERATE | c.278A>C | p.Lys93Thr | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 3/27 | 399/4664 | 278/4110 | 93/1369 | chr5 | 55297382 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:55261455 | G | A | 1 | a0001c0009 | 1 | HG00735.hp2 | synonymous_variant | LOW | c.3873C>T | p.Thr1291Thr | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 25/27 | 3994/4664 | 3873/4110 | 1291/1369 | chr5 | 55261455 | |||
| chr5:55262846 | G | A | 1 | a0001c0003 | 3 | HG00642.hp2 HG01167.hp2 HG01258.hp1 |
synonymous_variant | LOW | c.3612C>T | p.Ala1204Ala | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 24/27 | 3733/4664 | 3612/4110 | 1204/1369 | chr5 | 55262846 | |||
| chr5:55274966 | T | C | 1 | a0001c0012 | 1 | NA18972.hp1 | synonymous_variant | LOW | c.2472A>G | p.Pro824Pro | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 15/27 | 2593/4664 | 2472/4110 | 824/1369 | chr5 | 55274966 | |||
| chr5:55276335 | T | C | 5 | a0001c0002 a0001c0007 a0001c0013 others(2): Show |
86 | HG00423.hp2 HG00621.hp2 HG00733.hp2 others(83): Show |
synonymous_variant | LOW | c.2358A>G | p.Lys786Lys | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 14/27 | 2479/4664 | 2358/4110 | 786/1369 | chr5 | 55276335 | |||
| chr5:55276356 | T | C | 1 | a0001c0013 | 1 | NA18993.hp2 | synonymous_variant | LOW | c.2337A>G | p.Lys779Lys | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 14/27 | 2458/4664 | 2337/4110 | 779/1369 | chr5 | 55276356 | |||
| chr5:55277175 | G | A | 1 | a0001c0014 | 1 | NA18984.hp2 | synonymous_variant | LOW | c.2217C>T | p.Ser739Ser | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 13/27 | 2338/4664 | 2217/4110 | 739/1369 | chr5 | 55277175 | |||
| chr5:55283548 | T | C | 1 | a0001c0015 | 1 | NA18967.hp2 | synonymous_variant | LOW | c.1620A>G | p.Ser540Ser | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 11/27 | 1741/4664 | 1620/4110 | 540/1369 | chr5 | 55283548 | |||
| chr5:55289349 | A | C | 1 | a0009c0016 | 1 | NA18997.hp2 | synonymous_variant | LOW | c.987T>G | p.Pro329Pro | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 8/27 | 1108/4664 | 987/4110 | 329/1369 | chr5 | 55289349 | |||
| chr5:55289355 | T | C | 1 | a0009c0016 | 1 | NA18997.hp2 | synonymous_variant | LOW | c.981A>G | p.Lys327Lys | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 8/27 | 1102/4664 | 981/4110 | 327/1369 | chr5 | 55289355 | |||
| chr5:55289376 | T | G | 1 | a0009c0016 | 1 | NA18997.hp2 | synonymous_variant | LOW | c.960A>C | p.Ser320Ser | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 8/27 | 1081/4664 | 960/4110 | 320/1369 | chr5 | 55289376 | |||
| chr5:55290342 | A | G | 1 | a0002c0004 | 2 | HG01168.hp2 HG02717.hp2 |
splice_region_variant&synonymous_variant | LOW | c.783T>C | p.Asn261Asn | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 7/27 | 904/4664 | 783/4110 | 261/1369 | chr5 | 55290342 | |||
| chr5:55294104 | C | T | 1 | a0001c0007 | 1 | HG02145.hp2 | synonymous_variant | LOW | c.693G>A | p.Glu231Glu | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 6/27 | 814/4664 | 693/4110 | 231/1369 | chr5 | 55294104 | |||
| chr5:55307532 | C | G | 1 | a0001c0006 | 1 | HG02622.hp2 | synonymous_variant | LOW | c.42G>C | p.Ala14Ala | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 1/27 | 163/4664 | 42/4110 | 14/1369 | chr5 | 55307532 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:55256085 | G | A | 1 | a0002c0004t0004 | 2 | HG01168.hp2 HG02717.hp2 |
3_prime_UTR_variant | MODIFIER | c.*403C>T | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 27/27 | 403 | chr5 | 55256085 | ||||||
| chr5:55256231 | C | T | 4 | a0001c0001t0002 a0001c0012t0002 a0002c0004t0004 others(1): Show |
43 | HG00609.hp1 HG00741.hp1 HG01168.hp2 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*257G>A | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 27/27 | 257 | chr5 | 55256231 | ||||||
| chr5:55256239 | A | C | 1 | a0002c0004t0004 | 2 | HG01168.hp2 HG02717.hp2 |
3_prime_UTR_variant | MODIFIER | c.*249T>G | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 27/27 | 249 | chr5 | 55256239 | ||||||
| chr5:55307659 | C | T | 1 | a0001c0001t0003 | 2 | NA18950.hp1 NA19081.hp2 |
5_prime_UTR_variant | MODIFIER | c.-86G>A | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 1/27 | 86 | chr5 | 55307659 | ||||||
| chr5:55307672 | C | G | 1 | a0001c0001t0005 | 1 | HG01346.hp1 | 5_prime_UTR_variant | MODIFIER | c.-99G>C | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 1/27 | 99 | chr5 | 55307672 | ||||||
| chr5:55307673 | T | G | 1 | a0001c0001t0005 | 1 | HG01346.hp1 | 5_prime_UTR_variant | MODIFIER | c.-100A>C | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 1/27 | 100 | chr5 | 55307673 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:55256588 | A | G | 5 | a0001c0001t0001g0174 a0001c0002t0001g0040 a0001c0002t0001g0041 others(2): Show |
5 | HG02486.hp1 HG02895.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.4058-48T>C | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 26/26 | chr5 | 55256588 | |||||||
| chr5:55256778 | A | G | 2 | a0001c0001t0001g0061 a0001c0001t0001g0063 |
2 | HG01123.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.4058-238T>C | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 26/26 | chr5 | 55256778 | |||||||
| chr5:55256899 | T | G | 2 | a0002c0004t0004g0042 a0002c0004t0004g0043 |
2 | HG01168.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.4058-359A>C | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 26/26 | chr5 | 55256899 | |||||||
| chr5:55257066 | C | CG | 3 | a0001c0001t0001g0024 a0001c0001t0001g0149 a0001c0001t0001g0169 |
4 | HG01106.hp2 HG01358.hp2 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.4058-527dupC | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 26/26 | chr5 | 55257066 | |||||||
| chr5:55257116 | T | C | 1 | a0001c0001t0001g0094 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.4058-576A>G | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 26/26 | chr5 | 55257116 | |||||||
| chr5:55257304 | C | T | 7 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0066 others(4): Show |
10 | HG00642.hp1 HG00733.hp1 HG00735.hp2 others(7): Show |
intron_variant | MODIFIER | c.4058-764G>A | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 26/26 | chr5 | 55257304 | |||||||
| chr5:55257422 | C | T | 5 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0136 others(2): Show |
5 | HG02523.hp2 NA18941.hp2 NA19005.hp2 others(2): Show |
intron_variant | MODIFIER | c.4058-882G>A | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 26/26 | chr5 | 55257422 | |||||||
| chr5:55257559 | G | C | 2 | a0001c0001t0001g0022 a0001c0001t0001g0179 |
3 | HG02129.hp1 NA18989.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.4058-1019C>G | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 26/26 | chr5 | 55257559 | |||||||
| chr5:55257628 | A | G | 1 | a0001c0001t0001g0166 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.4058-1088T>C | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 26/26 | chr5 | 55257628 | |||||||
| chr5:55257737 | C | A | 2 | a0001c0001t0001g0024 a0001c0001t0001g0149 |
3 | HG01106.hp2 HG01358.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.4058-1197G>T | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 26/26 | chr5 | 55257737 | |||||||
| chr5:55258044 | G | C | 2 | a0001c0002t0001g0040 a0001c0002t0001g0041 |
2 | HG02486.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.4058-1504C>G | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 26/26 | chr5 | 55258044 | |||||||
| chr5:55258193 | C | T | 3 | a0001c0003t0001g0071 a0001c0003t0001g0092 a0001c0003t0001g0114 |
3 | HG00642.hp2 HG01167.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.4058-1653G>A | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 26/26 | chr5 | 55258193 | |||||||
| chr5:55258406 | C | G | 1 | a0001c0001t0001g0075 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.4057+1442G>C | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 26/26 | chr5 | 55258406 | |||||||
| chr5:55258718 | C | T | 206 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(203): Show |
264 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(261): Show |
intron_variant | MODIFIER | c.4057+1130G>A | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 26/26 | chr5 | 55258718 | |||||||
| chr5:55258751 | C | T | 1 | a0001c0001t0001g0066 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.4057+1097G>A | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 26/26 | chr5 | 55258751 | |||||||
| chr5:55259232 | C | T | 2 | a0001c0002t0001g0228 a0001c0002t0001g0230 |
2 | NA18947.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.4057+616G>A | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 26/26 | chr5 | 55259232 | |||||||
| chr5:55259526 | C | T | 3 | a0001c0002t0001g0037 a0001c0002t0001g0038 a0001c0002t0001g0039 |
3 | HG02109.hp2 HG02615.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.4057+322G>A | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 26/26 | chr5 | 55259526 | |||||||
| chr5:55259543 | G | A | 5 | a0001c0002t0001g0007 a0001c0002t0001g0225 a0001c0002t0001g0234 others(2): Show |
8 | HG02155.hp2 NA18747.hp2 NA18957.hp1 others(5): Show |
intron_variant | MODIFIER | c.4057+305C>T | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 26/26 | chr5 | 55259543 | |||||||
| chr5:55259685 | A | G | 29 | a0001c0001t0002g0006 a0001c0001t0002g0010 a0001c0001t0002g0011 others(26): Show |
41 | HG00609.hp1 HG00741.hp1 HG01433.hp1 others(38): Show |
intron_variant | MODIFIER | c.4057+163T>C | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 26/26 | chr5 | 55259685 | |||||||
| chr5:55259747 | G | A | 1 | a0001c0001t0001g0021 | 2 | HG00597.hp2 HG02027.hp2 |
intron_variant | MODIFIER | c.4057+101C>T | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 26/26 | chr5 | 55259747 | |||||||
| chr5:55259750 | CCT | C | 31 | a0001c0001t0002g0006 a0001c0001t0002g0010 a0001c0001t0002g0011 others(28): Show |
43 | HG00609.hp1 HG00741.hp1 HG01168.hp2 others(40): Show |
intron_variant | MODIFIER | c.4057+96_4057+97del others(2): Show |
DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 26/26 | chr5 | 55259750 | |||||||
| chr5:55259987 | C | G | 31 | a0001c0001t0002g0006 a0001c0001t0002g0010 a0001c0001t0002g0011 others(28): Show |
43 | HG00609.hp1 HG00741.hp1 HG01168.hp2 others(40): Show |
intron_variant | MODIFIER | c.3961-43G>C | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 25/26 | chr5 | 55259987 | |||||||
| chr5:55260021 | C | A | 31 | a0001c0001t0002g0006 a0001c0001t0002g0010 a0001c0001t0002g0011 others(28): Show |
43 | HG00609.hp1 HG00741.hp1 HG01168.hp2 others(40): Show |
intron_variant | MODIFIER | c.3961-77G>T | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 25/26 | chr5 | 55260021 | |||||||
| chr5:55260136 | G | A | 2 | a0001c0002t0001g0250 a0001c0002t0001g0251 |
2 | HG02735.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.3961-192C>T | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 25/26 | chr5 | 55260136 | |||||||
| chr5:55260419 | G | C | 2 | a0002c0004t0004g0042 a0002c0004t0004g0043 |
2 | HG01168.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.3961-475C>G | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 25/26 | chr5 | 55260419 | |||||||
| chr5:55260460 | T | G | 1 | a0003c0005t0001g0054 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3961-516A>C | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 25/26 | chr5 | 55260460 | |||||||
| chr5:55260527 | G | GGCCTGGG others(20): Show |
31 | a0001c0001t0002g0006 a0001c0001t0002g0010 a0001c0001t0002g0011 others(28): Show |
43 | HG00609.hp1 HG00741.hp1 HG01168.hp2 others(40): Show |
intron_variant | MODIFIER | c.3961-584_3961-583i others(29): Show |
DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 25/26 | chr5 | 55260527 | |||||||
| chr5:55260527 | G | GGCCTGGG others(20): Show |
175 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(172): Show |
221 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(218): Show |
intron_variant | MODIFIER | c.3961-584_3961-583i others(29): Show |
DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 25/26 | chr5 | 55260527 | |||||||
| chr5:55260606 | A | G | 206 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(203): Show |
264 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(261): Show |
intron_variant | MODIFIER | c.3961-662T>C | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 25/26 | chr5 | 55260606 | |||||||
| chr5:55260624 | T | G | 31 | a0001c0001t0002g0006 a0001c0001t0002g0010 a0001c0001t0002g0011 others(28): Show |
43 | HG00609.hp1 HG00741.hp1 HG01168.hp2 others(40): Show |
intron_variant | MODIFIER | c.3961-680A>C | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 25/26 | chr5 | 55260624 | |||||||
| chr5:55260738 | A | C | 10 | a0001c0001t0001g0048 a0001c0001t0001g0050 a0001c0001t0001g0051 others(7): Show |
10 | HG01243.hp1 HG02109.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.3960+630T>G | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 25/26 | chr5 | 55260738 | |||||||
| chr5:55260803 | G | C | 1 | a0001c0001t0001g0165 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.3960+565C>G | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 25/26 | chr5 | 55260803 | |||||||
| chr5:55260916 | C | G | 1 | a0001c0001t0002g0197 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.3960+452G>C | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 25/26 | chr5 | 55260916 | |||||||
| chr5:55260968 | G | C | 2 | a0001c0001t0002g0198 a0001c0001t0002g0207 |
2 | NA18947.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.3960+400C>G | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 25/26 | chr5 | 55260968 | |||||||
| chr5:55261060 | T | C | 5 | a0001c0001t0001g0174 a0001c0002t0001g0040 a0001c0002t0001g0041 others(2): Show |
5 | HG02486.hp1 HG02895.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.3960+308A>G | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 25/26 | chr5 | 55261060 | |||||||
| chr5:55261062 | G | A | 3 | a0001c0001t0001g0260 a0001c0001t0001g0262 a0009c0016t0001g0259 |
3 | NA18991.hp2 NA18997.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.3960+306C>T | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 25/26 | chr5 | 55261062 | |||||||
| chr5:55261152 | T | C | 6 | a0001c0002t0001g0209 a0001c0002t0001g0228 a0001c0002t0001g0229 others(3): Show |
6 | NA18947.hp2 NA18968.hp2 NA19000.hp1 others(3): Show |
intron_variant | MODIFIER | c.3960+216A>G | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 25/26 | chr5 | 55261152 | |||||||
| chr5:55261203 | A | C | 1 | a0001c0001t0001g0076 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.3960+165T>G | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 25/26 | chr5 | 55261203 | |||||||
| chr5:55261204 | A | T | 2 | a0002c0004t0004g0042 a0002c0004t0004g0043 |
2 | HG01168.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.3960+164T>A | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 25/26 | chr5 | 55261204 | |||||||
| chr5:55261318 | C | T | 51 | a0001c0001t0001g0005 a0001c0001t0001g0021 a0001c0001t0001g0022 others(48): Show |
60 | HG00140.hp1 HG00423.hp1 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.3960+50G>A | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 25/26 | chr5 | 55261318 | |||||||
| chr5:55261845 | C | T | 1 | a0001c0002t0001g0250 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.3829-346G>A | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 24/26 | chr5 | 55261845 | |||||||
| chr5:55261880 | C | CAT | 31 | a0001c0001t0002g0006 a0001c0001t0002g0010 a0001c0001t0002g0011 others(28): Show |
43 | HG00609.hp1 HG00741.hp1 HG01168.hp2 others(40): Show |
intron_variant | MODIFIER | c.3829-382_3829-381i others(4): Show |
DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 24/26 | chr5 | 55261880 | |||||||
| chr5:55261966 | A | G | 1 | a0001c0001t0001g0087 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.3829-467T>C | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 24/26 | chr5 | 55261966 | |||||||
| chr5:55262118 | A | G | 3 | a0001c0001t0001g0260 a0001c0001t0001g0262 a0009c0016t0001g0259 |
3 | NA18991.hp2 NA18997.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.3828+512T>C | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 24/26 | chr5 | 55262118 | |||||||
| chr5:55262541 | A | G | 29 | a0001c0001t0002g0006 a0001c0001t0002g0010 a0001c0001t0002g0011 others(26): Show |
41 | HG00609.hp1 HG00741.hp1 HG01433.hp1 others(38): Show |
intron_variant | MODIFIER | c.3828+89T>C | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 24/26 | chr5 | 55262541 | |||||||
| chr5:55263033 | G | T | 2 | a0002c0004t0004g0042 a0002c0004t0004g0043 |
2 | HG01168.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.3526-101C>A | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 23/26 | chr5 | 55263033 | |||||||
| chr5:55263038 | T | C | 2 | a0001c0002t0001g0224 a0001c0002t0001g0226 |
2 | NA18971.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.3526-106A>G | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 23/26 | chr5 | 55263038 | |||||||
| chr5:55263144 | G | A | 31 | a0001c0001t0002g0006 a0001c0001t0002g0010 a0001c0001t0002g0011 others(28): Show |
43 | HG00609.hp1 HG00741.hp1 HG01168.hp2 others(40): Show |
intron_variant | MODIFIER | c.3526-212C>T | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 23/26 | chr5 | 55263144 | |||||||
| chr5:55263219 | C | A | 1 | a0001c0001t0001g0083 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.3526-287G>T | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 23/26 | chr5 | 55263219 | |||||||
| chr5:55263434 | T | C | 31 | a0001c0001t0002g0006 a0001c0001t0002g0010 a0001c0001t0002g0011 others(28): Show |
43 | HG00609.hp1 HG00741.hp1 HG01168.hp2 others(40): Show |
intron_variant | MODIFIER | c.3526-502A>G | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 23/26 | chr5 | 55263434 | |||||||
| chr5:55263479 | C | A | 4 | a0001c0002t0001g0254 a0001c0002t0001g0257 a0001c0002t0001g0258 others(1): Show |
4 | HG02145.hp2 HG02922.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.3526-547G>T | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 23/26 | chr5 | 55263479 | |||||||
| chr5:55263493 | C | T | 1 | a0001c0001t0001g0089 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3526-561G>A | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 23/26 | chr5 | 55263493 | |||||||
| chr5:55263565 | G | T | 2 | a0001c0001t0001g0093 a0001c0001t0001g0094 |
2 | HG01192.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.3526-633C>A | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 23/26 | chr5 | 55263565 | |||||||
| chr5:55263580 | G | C | 4 | a0001c0001t0001g0023 a0001c0001t0001g0049 a0001c0001t0001g0162 others(1): Show |
5 | HG02055.hp2 HG02970.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.3526-648C>G | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 23/26 | chr5 | 55263580 | |||||||
| chr5:55263582 | A | G | 31 | a0001c0001t0002g0006 a0001c0001t0002g0010 a0001c0001t0002g0011 others(28): Show |
43 | HG00609.hp1 HG00741.hp1 HG01168.hp2 others(40): Show |
intron_variant | MODIFIER | c.3526-650T>C | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 23/26 | chr5 | 55263582 | |||||||
| chr5:55263950 | A | C | 1 | a0001c0001t0001g0126 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3526-1018T>G | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 23/26 | chr5 | 55263950 | |||||||
| chr5:55264018 | A | G | 160 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(157): Show |
206 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(203): Show |
intron_variant | MODIFIER | c.3526-1086T>C | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 23/26 | chr5 | 55264018 | |||||||
| chr5:55264034 | C | T | 2 | a0002c0004t0004g0042 a0002c0004t0004g0043 |
2 | HG01168.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.3526-1102G>A | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 23/26 | chr5 | 55264034 | |||||||
| chr5:55264170 | C | T | 31 | a0001c0001t0002g0006 a0001c0001t0002g0010 a0001c0001t0002g0011 others(28): Show |
43 | HG00609.hp1 HG00741.hp1 HG01168.hp2 others(40): Show |
intron_variant | MODIFIER | c.3526-1238G>A | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 23/26 | chr5 | 55264170 | |||||||
| chr5:55264218 | G | A | 8 | a0001c0001t0001g0003 a0001c0001t0001g0044 a0001c0001t0001g0097 others(5): Show |
12 | HG01109.hp2 HG01515.hp2 HG01517.hp2 others(9): Show |
intron_variant | MODIFIER | c.3526-1286C>T | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 23/26 | chr5 | 55264218 | |||||||
| chr5:55264270 | T | A | 18 | a0001c0001t0002g0006 a0001c0001t0002g0011 a0001c0001t0002g0012 others(15): Show |
25 | HG00609.hp1 HG00741.hp1 HG01433.hp1 others(22): Show |
intron_variant | MODIFIER | c.3526-1338A>T | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 23/26 | chr5 | 55264270 | |||||||
| chr5:55264382 | C | T | 29 | a0001c0001t0002g0006 a0001c0001t0002g0010 a0001c0001t0002g0011 others(26): Show |
41 | HG00609.hp1 HG00741.hp1 HG01433.hp1 others(38): Show |
intron_variant | MODIFIER | c.3526-1450G>A | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 23/26 | chr5 | 55264382 | |||||||
| chr5:55264461 | G | A | 170 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(167): Show |
216 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(213): Show |
intron_variant | MODIFIER | c.3526-1529C>T | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 23/26 | chr5 | 55264461 | |||||||
| chr5:55264496 | C | T | 2 | a0001c0002t0001g0013 a0001c0002t0001g0227 |
4 | HG00423.hp2 NA18948.hp2 NA18960.hp2 others(1): Show |
intron_variant | MODIFIER | c.3526-1564G>A | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 23/26 | chr5 | 55264496 | |||||||
| chr5:55264584 | T | C | 31 | a0001c0001t0002g0006 a0001c0001t0002g0010 a0001c0001t0002g0011 others(28): Show |
43 | HG00609.hp1 HG00741.hp1 HG01168.hp2 others(40): Show |
intron_variant | MODIFIER | c.3526-1652A>G | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 23/26 | chr5 | 55264584 | |||||||
| chr5:55264663 | T | TA | 15 | a0001c0002t0001g0004 a0001c0002t0001g0013 a0001c0002t0001g0209 others(12): Show |
21 | HG00423.hp2 HG00621.hp2 HG02074.hp2 others(18): Show |
intron_variant | MODIFIER | c.3526-1732dupT | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 23/26 | chr5 | 55264663 | |||||||
| chr5:55264677 | C | A | 29 | a0001c0001t0002g0006 a0001c0001t0002g0010 a0001c0001t0002g0011 others(26): Show |
41 | HG00609.hp1 HG00741.hp1 HG01433.hp1 others(38): Show |
intron_variant | MODIFIER | c.3526-1745G>T | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 23/26 | chr5 | 55264677 | |||||||
| chr5:55264844 | C | CTGG | 3 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0127 |
3 | NA18612.hp2 NA18955.hp1 NA18978.hp1 |
intron_variant | MODIFIER | c.3526-1913_3526-191 others(7): Show |
DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 23/26 | chr5 | 55264844 | |||||||
| chr5:55264850 | C | T | 2 | a0001c0001t0001g0046 a0001c0001t0001g0125 |
2 | HG02129.hp2 NA18957.hp2 |
intron_variant | MODIFIER | c.3526-1918G>A | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 23/26 | chr5 | 55264850 | |||||||
| chr5:55265094 | GA | G | 198 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(195): Show |
256 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(253): Show |
intron_variant | MODIFIER | c.3525+2043delT | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 23/26 | chr5 | 55265094 | |||||||
| chr5:55265301 | A | G | 1 | a0001c0001t0001g0109 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.3525+1837T>C | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 23/26 | chr5 | 55265301 | |||||||
| chr5:55265395 | A | G | 1 | a0001c0002t0001g0224 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.3525+1743T>C | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 23/26 | chr5 | 55265395 | |||||||
| chr5:55265536 | G | C | 31 | a0001c0001t0002g0006 a0001c0001t0002g0010 a0001c0001t0002g0011 others(28): Show |
43 | HG00609.hp1 HG00741.hp1 HG01168.hp2 others(40): Show |
intron_variant | MODIFIER | c.3525+1602C>G | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 23/26 | chr5 | 55265536 | |||||||
| chr5:55265571 | C | A | 3 | a0001c0001t0001g0174 a0003c0005t0001g0054 a0003c0005t0001g0055 |
3 | HG03130.hp2 HG03209.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.3525+1567G>T | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 23/26 | chr5 | 55265571 | |||||||
| chr5:55265571 | C | T | 29 | a0001c0001t0002g0006 a0001c0001t0002g0010 a0001c0001t0002g0011 others(26): Show |
41 | HG00609.hp1 HG00741.hp1 HG01433.hp1 others(38): Show |
intron_variant | MODIFIER | c.3525+1567G>A | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 23/26 | chr5 | 55265571 | |||||||
| chr5:55265670 | T | TA | 158 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(155): Show |
203 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(200): Show |
intron_variant | MODIFIER | c.3525+1467dupT | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 23/26 | chr5 | 55265670 | |||||||
| chr5:55265670 | TA | T | 31 | a0001c0001t0001g0174 a0001c0001t0002g0006 a0001c0001t0002g0010 others(28): Show |
43 | HG00609.hp1 HG00741.hp1 HG01433.hp1 others(40): Show |
intron_variant | MODIFIER | c.3525+1467delT | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 23/26 | chr5 | 55265670 | |||||||
| chr5:55265749 | T | C | 2 | a0001c0001t0001g0050 a0001c0001t0001g0053 |
2 | HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.3525+1389A>G | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 23/26 | chr5 | 55265749 | |||||||
| chr5:55265815 | G | A | 201 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(198): Show |
259 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(256): Show |
intron_variant | MODIFIER | c.3525+1323C>T | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 23/26 | chr5 | 55265815 | |||||||
| chr5:55265857 | C | T | 29 | a0001c0001t0002g0006 a0001c0001t0002g0010 a0001c0001t0002g0011 others(26): Show |
41 | HG00609.hp1 HG00741.hp1 HG01433.hp1 others(38): Show |
intron_variant | MODIFIER | c.3525+1281G>A | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 23/26 | chr5 | 55265857 | |||||||
| chr5:55265863 | G | C | 1 | a0001c0001t0001g0126 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3525+1275C>G | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 23/26 | chr5 | 55265863 | |||||||
| chr5:55265918 | G | T | 1 | a0001c0002t0001g0255 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3525+1220C>A | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 23/26 | chr5 | 55265918 | |||||||
| chr5:55265940 | T | C | 2 | a0001c0001t0001g0067 a0001c0001t0001g0068 |
2 | HG01255.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.3525+1198A>G | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 23/26 | chr5 | 55265940 | |||||||
| chr5:55266031 | G | A | 1 | a0001c0002t0001g0037 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.3525+1107C>T | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 23/26 | chr5 | 55266031 | |||||||
| chr5:55266075 | T | C | 29 | a0001c0001t0002g0006 a0001c0001t0002g0010 a0001c0001t0002g0011 others(26): Show |
41 | HG00609.hp1 HG00741.hp1 HG01433.hp1 others(38): Show |
intron_variant | MODIFIER | c.3525+1063A>G | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 23/26 | chr5 | 55266075 | |||||||
| chr5:55266310 | GT | G | 33 | a0001c0001t0001g0050 a0001c0001t0001g0053 a0001c0001t0002g0006 others(30): Show |
45 | HG00609.hp1 HG00741.hp1 HG01168.hp2 others(42): Show |
intron_variant | MODIFIER | c.3525+827delA | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 23/26 | chr5 | 55266310 | |||||||
| chr5:55266332 | G | A | 4 | a0001c0001t0001g0147 a0001c0001t0001g0175 a0001c0001t0001g0176 others(1): Show |
4 | HG01123.hp1 HG01256.hp2 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.3525+806C>T | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 23/26 | chr5 | 55266332 | |||||||
| chr5:55266497 | C | T | 1 | a0001c0002t0001g0220 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.3525+641G>A | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 23/26 | chr5 | 55266497 | |||||||
| chr5:55266548 | A | ATTTTTT | 28 | a0001c0001t0002g0006 a0001c0001t0002g0010 a0001c0001t0002g0011 others(25): Show |
40 | HG00609.hp1 HG00741.hp1 HG01433.hp1 others(37): Show |
intron_variant | MODIFIER | c.3525+584_3525+589d others(8): Show |
DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 23/26 | chr5 | 55266548 | |||||||
| chr5:55266595 | T | C | 2 | a0002c0004t0004g0042 a0002c0004t0004g0043 |
2 | HG01168.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.3525+543A>G | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 23/26 | chr5 | 55266595 | |||||||
| chr5:55266690 | A | C | 2 | a0001c0002t0001g0040 a0001c0002t0001g0041 |
2 | HG02486.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.3525+448T>G | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 23/26 | chr5 | 55266690 | |||||||
| chr5:55266804 | C | T | 1 | a0001c0001t0001g0058 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.3525+334G>A | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 23/26 | chr5 | 55266804 | |||||||
| chr5:55266904 | T | C | 32 | a0001c0001t0001g0022 a0001c0001t0001g0179 a0001c0001t0002g0006 others(29): Show |
43 | HG00609.hp1 HG00741.hp1 HG01433.hp1 others(40): Show |
intron_variant | MODIFIER | c.3525+234A>G | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 23/26 | chr5 | 55266904 | |||||||
| chr5:55266992 | AG | A | 31 | a0001c0001t0002g0006 a0001c0001t0002g0010 a0001c0001t0002g0011 others(28): Show |
43 | HG00609.hp1 HG00741.hp1 HG01433.hp1 others(40): Show |
intron_variant | MODIFIER | c.3525+145delC | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 23/26 | chr5 | 55266992 | |||||||
| chr5:55267096 | G | A | 1 | a0001c0001t0001g0062 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.3525+42C>T | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 23/26 | chr5 | 55267096 | |||||||
| chr5:55267414 | G | A | 28 | a0001c0001t0002g0006 a0001c0001t0002g0011 a0001c0001t0002g0012 others(25): Show |
38 | HG00609.hp1 HG00741.hp1 HG01168.hp2 others(35): Show |
intron_variant | MODIFIER | c.3432-183C>T | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 22/26 | chr5 | 55267414 | |||||||
| chr5:55267645 | A | G | 5 | a0001c0001t0001g0050 a0001c0001t0001g0053 a0001c0001t0001g0057 others(2): Show |
5 | HG01106.hp1 HG02486.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.3431+41T>C | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 22/26 | chr5 | 55267645 | |||||||
| chr5:55267652 | T | C | 6 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0066 others(3): Show |
9 | HG00642.hp1 HG00733.hp1 HG00735.hp2 others(6): Show |
intron_variant | MODIFIER | c.3431+34A>G | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 22/26 | chr5 | 55267652 | |||||||
| chr5:55267894 | G | T | 1 | a0001c0001t0002g0190 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.3295-72C>A | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 21/26 | chr5 | 55267894 | |||||||
| chr5:55267947 | TTTA | T | 105 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(102): Show |
142 | HG00140.hp2 HG00597.hp1 HG00609.hp2 others(139): Show |
intron_variant | MODIFIER | c.3295-128_3295-126d others(5): Show |
DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 21/26 | chr5 | 55267947 | |||||||
| chr5:55268101 | G | A | 1 | a0001c0001t0001g0176 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.3295-279C>T | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 21/26 | chr5 | 55268101 | |||||||
| chr5:55268114 | C | T | 4 | a0001c0002t0001g0040 a0001c0002t0001g0041 a0003c0005t0001g0054 others(1): Show |
4 | HG02486.hp1 HG02895.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.3295-292G>A | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 21/26 | chr5 | 55268114 | |||||||
| chr5:55268481 | G | A | 2 | a0001c0001t0001g0134 a0001c0001t0001g0137 |
2 | NA18941.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.3295-659C>T | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 21/26 | chr5 | 55268481 | |||||||
| chr5:55268573 | C | T | 2 | a0002c0004t0004g0042 a0002c0004t0004g0043 |
2 | HG01168.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.3295-751G>A | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 21/26 | chr5 | 55268573 | |||||||
| chr5:55268715 | C | CTGGAATG others(12): Show |
2 | a0002c0004t0004g0042 a0002c0004t0004g0043 |
2 | HG01168.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.3294+697_3294+698i others(21): Show |
DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 21/26 | chr5 | 55268715 | |||||||
| chr5:55268717 | T | A | 2 | a0002c0004t0004g0042 a0002c0004t0004g0043 |
2 | HG01168.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.3294+696A>T | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 21/26 | chr5 | 55268717 | |||||||
| chr5:55268798 | C | G | 1 | a0001c0001t0001g0084 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.3294+615G>C | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 21/26 | chr5 | 55268798 | |||||||
| chr5:55268809 | G | C | 2 | a0002c0004t0004g0042 a0002c0004t0004g0043 |
2 | HG01168.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.3294+604C>G | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 21/26 | chr5 | 55268809 | |||||||
| chr5:55268835 | T | G | 1 | a0001c0001t0002g0190 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.3294+578A>C | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 21/26 | chr5 | 55268835 | |||||||
| chr5:55269243 | C | CA | 12 | a0001c0001t0001g0025 a0001c0001t0001g0090 a0001c0001t0001g0105 others(9): Show |
13 | HG02074.hp1 HG02897.hp1 HG02976.hp2 others(10): Show |
intron_variant | MODIFIER | c.3294+169dupT | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 21/26 | chr5 | 55269243 | |||||||
| chr5:55269243 | C | CAA | 51 | a0001c0002t0001g0002 a0001c0002t0001g0004 a0001c0002t0001g0007 others(48): Show |
70 | HG00423.hp2 HG00621.hp2 HG00733.hp2 others(67): Show |
intron_variant | MODIFIER | c.3294+168_3294+169d others(4): Show |
DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 21/26 | chr5 | 55269243 | |||||||
| chr5:55269243 | C | CAAA | 7 | a0001c0002t0001g0209 a0001c0002t0001g0219 a0001c0002t0001g0230 others(4): Show |
7 | HG02145.hp2 HG03209.hp1 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.3294+167_3294+169d others(5): Show |
DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 21/26 | chr5 | 55269243 | |||||||
| chr5:55269298 | C | A | 2 | a0002c0004t0004g0042 a0002c0004t0004g0043 |
2 | HG01168.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.3294+115G>T | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 21/26 | chr5 | 55269298 | |||||||
| chr5:55269355 | G | A | 2 | a0001c0001t0001g0057 a0001c0001t0001g0091 |
2 | HG01074.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.3294+58C>T | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 21/26 | chr5 | 55269355 | |||||||
| chr5:55269775 | TA | T | 2 | a0001c0001t0002g0010 a0001c0001t0002g0193 |
4 | HG02280.hp2 HG03516.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.3070-139delT | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 20/26 | chr5 | 55269775 | |||||||
| chr5:55269940 | T | C | 1 | a0001c0001t0001g0115 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.3070-303A>G | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 20/26 | chr5 | 55269940 | |||||||
| chr5:55270393 | C | A | 2 | a0002c0004t0004g0042 a0002c0004t0004g0043 |
2 | HG01168.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.3069+19G>T | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 20/26 | chr5 | 55270393 | |||||||
| chr5:55270998 | T | C | 2 | a0002c0004t0004g0042 a0002c0004t0004g0043 |
2 | HG01168.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.2865-292A>G | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 18/26 | chr5 | 55270998 | |||||||
| chr5:55271064 | C | T | 3 | a0001c0002t0001g0037 a0001c0002t0001g0038 a0001c0002t0001g0039 |
3 | HG02109.hp2 HG02615.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2865-358G>A | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 18/26 | chr5 | 55271064 | |||||||
| chr5:55271409 | T | C | 1 | a0001c0002t0001g0255 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2864+678A>G | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 18/26 | chr5 | 55271409 | |||||||
| chr5:55271514 | T | C | 1 | a0001c0012t0002g0201 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.2864+573A>G | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 18/26 | chr5 | 55271514 | |||||||
| chr5:55271581 | C | T | 152 | a0001c0001t0001g0005 a0001c0001t0001g0021 a0001c0001t0001g0022 others(149): Show |
192 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(189): Show |
intron_variant | MODIFIER | c.2864+506G>A | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 18/26 | chr5 | 55271581 | |||||||
| chr5:55271597 | T | C | 1 | a0001c0001t0001g0113 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2864+490A>G | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 18/26 | chr5 | 55271597 | |||||||
| chr5:55271890 | A | G | 1 | a0001c0001t0001g0159 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2864+197T>C | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 18/26 | chr5 | 55271890 | |||||||
| chr5:55271994 | T | A | 1 | a0001c0001t0001g0126 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2864+93A>T | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 18/26 | chr5 | 55271994 | |||||||
| chr5:55272461 | G | A | 5 | a0001c0002t0001g0033 a0001c0002t0001g0244 a0001c0002t0001g0246 others(2): Show |
6 | HG02451.hp1 HG02559.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.2776-286C>T | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 17/26 | chr5 | 55272461 | |||||||
| chr5:55272644 | A | G | 1 | a0001c0001t0001g0165 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2776-469T>C | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 17/26 | chr5 | 55272644 | |||||||
| chr5:55272826 | A | G | 49 | a0001c0002t0001g0002 a0001c0002t0001g0004 a0001c0002t0001g0007 others(46): Show |
68 | HG00423.hp2 HG00621.hp2 HG00733.hp2 others(65): Show |
intron_variant | MODIFIER | c.2775+467T>C | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 17/26 | chr5 | 55272826 | |||||||
| chr5:55272840 | T | C | 1 | a0001c0001t0001g0174 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2775+453A>G | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 17/26 | chr5 | 55272840 | |||||||
| chr5:55272899 | A | G | 5 | a0001c0002t0001g0040 a0001c0002t0001g0041 a0001c0002t0001g0252 others(2): Show |
5 | HG02280.hp1 HG02486.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.2775+394T>C | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 17/26 | chr5 | 55272899 | |||||||
| chr5:55272993 | CCTTCTTG others(14): Show |
C | 2 | a0002c0004t0004g0042 a0002c0004t0004g0043 |
2 | HG01168.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.2775+279_2775+299d others(23): Show |
DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 17/26 | chr5 | 55272993 | |||||||
| chr5:55273234 | C | T | 50 | a0001c0001t0001g0005 a0001c0001t0001g0021 a0001c0001t0001g0022 others(47): Show |
59 | HG00140.hp1 HG00423.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.2775+59G>A | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 17/26 | chr5 | 55273234 | |||||||
| chr5:55273693 | G | A | 2 | a0002c0004t0004g0042 a0002c0004t0004g0043 |
2 | HG01168.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.2691-316C>T | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 16/26 | chr5 | 55273693 | |||||||
| chr5:55273814 | C | T | 47 | a0001c0001t0001g0005 a0001c0001t0001g0021 a0001c0001t0001g0022 others(44): Show |
56 | HG00140.hp1 HG00423.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.2691-437G>A | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 16/26 | chr5 | 55273814 | |||||||
| chr5:55273890 | C | T | 1 | a0001c0002t0001g0215 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.2691-513G>A | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 16/26 | chr5 | 55273890 | |||||||
| chr5:55273977 | C | T | 1 | a0001c0001t0001g0082 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.2691-600G>A | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 16/26 | chr5 | 55273977 | |||||||
| chr5:55274013 | G | A | 6 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(3): Show |
6 | HG01243.hp1 HG03041.hp2 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.2690+601C>T | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 16/26 | chr5 | 55274013 | |||||||
| chr5:55274086 | C | CA | 14 | a0001c0001t0001g0009 a0001c0001t0001g0048 a0001c0001t0001g0049 others(11): Show |
16 | HG00642.hp2 HG01167.hp2 HG01258.hp1 others(13): Show |
intron_variant | MODIFIER | c.2690+527dupT | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 16/26 | chr5 | 55274086 | |||||||
| chr5:55274086 | CAAAAAAA others(4): Show |
C | 29 | a0001c0001t0002g0006 a0001c0001t0002g0010 a0001c0001t0002g0011 others(26): Show |
41 | HG00609.hp1 HG00741.hp1 HG01433.hp1 others(38): Show |
intron_variant | MODIFIER | c.2690+517_2690+527d others(13): Show |
DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 16/26 | chr5 | 55274086 | |||||||
| chr5:55274125 | G | A | 1 | a0001c0002t0001g0242 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2690+489C>T | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 16/26 | chr5 | 55274125 | |||||||
| chr5:55274129 | C | T | 1 | a0001c0001t0001g0082 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.2690+485G>A | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 16/26 | chr5 | 55274129 | |||||||
| chr5:55274209 | C | G | 2 | a0002c0004t0004g0042 a0002c0004t0004g0043 |
2 | HG01168.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.2690+405G>C | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 16/26 | chr5 | 55274209 | |||||||
| chr5:55274221 | T | C | 4 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0095 others(1): Show |
4 | HG00741.hp2 HG01071.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.2690+393A>G | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 16/26 | chr5 | 55274221 | |||||||
| chr5:55274427 | T | C | 2 | a0002c0004t0004g0042 a0002c0004t0004g0043 |
2 | HG01168.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.2690+187A>G | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 16/26 | chr5 | 55274427 | |||||||
| chr5:55274438 | A | C | 6 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(3): Show |
6 | HG01243.hp1 HG03041.hp2 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.2690+176T>G | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 16/26 | chr5 | 55274438 | |||||||
| chr5:55274548 | G | T | 2 | a0001c0001t0001g0168 a0001c0001t0001g0178 |
2 | NA18999.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.2690+66C>A | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 16/26 | chr5 | 55274548 | |||||||
| chr5:55274855 | T | C | 1 | a0001c0001t0001g0102 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2572+11A>G | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 15/26 | chr5 | 55274855 | |||||||
| chr5:55275108 | A | G | 1 | a0001c0001t0002g0202 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2428-98T>C | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 14/26 | chr5 | 55275108 | |||||||
| chr5:55275302 | T | A | 1 | a0001c0002t0001g0240 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2428-292A>T | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 14/26 | chr5 | 55275302 | |||||||
| chr5:55275317 | G | A | 1 | a0001c0002t0001g0248 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2428-307C>T | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 14/26 | chr5 | 55275317 | |||||||
| chr5:55275336 | G | A | 5 | a0001c0002t0001g0040 a0001c0002t0001g0041 a0001c0002t0001g0252 others(2): Show |
5 | HG02280.hp1 HG02486.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.2428-326C>T | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 14/26 | chr5 | 55275336 | |||||||
| chr5:55275410 | G | A | 161 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0020 others(158): Show |
204 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(201): Show |
intron_variant | MODIFIER | c.2428-400C>T | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 14/26 | chr5 | 55275410 | |||||||
| chr5:55275436 | C | T | 2 | a0002c0004t0004g0042 a0002c0004t0004g0043 |
2 | HG01168.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.2428-426G>A | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 14/26 | chr5 | 55275436 | |||||||
| chr5:55275698 | G | C | 1 | a0001c0001t0001g0123 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.2427+568C>G | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 14/26 | chr5 | 55275698 | |||||||
| chr5:55275725 | C | CTATG | 28 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0049 others(25): Show |
37 | HG01099.hp2 HG01123.hp1 HG01256.hp2 others(34): Show |
intron_variant | MODIFIER | c.2427+537_2427+540d others(6): Show |
DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 14/26 | chr5 | 55275725 | |||||||
| chr5:55275725 | CTATG | C | 27 | a0001c0001t0001g0003 a0001c0001t0001g0044 a0001c0001t0001g0050 others(24): Show |
33 | HG00733.hp2 HG01109.hp2 HG01515.hp2 others(30): Show |
intron_variant | MODIFIER | c.2427+537_2427+540d others(6): Show |
DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 14/26 | chr5 | 55275725 | |||||||
| chr5:55275725 | CTATGTAT others(5): Show |
C | 3 | a0001c0001t0001g0064 a0001c0001t0001g0074 a0001c0001t0001g0075 |
3 | HG02572.hp1 NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2427+529_2427+540d others(14): Show |
DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 14/26 | chr5 | 55275725 | |||||||
| chr5:55275771 | A | G | 1 | a0001c0001t0001g0143 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.2427+495T>C | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 14/26 | chr5 | 55275771 | |||||||
| chr5:55275927 | A | AG | 153 | a0001c0001t0001g0005 a0001c0001t0001g0021 a0001c0001t0001g0022 others(150): Show |
193 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(190): Show |
intron_variant | MODIFIER | c.2427+338dupC | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 14/26 | chr5 | 55275927 | |||||||
| chr5:55276026 | G | A | 4 | a0001c0002t0001g0037 a0001c0002t0001g0038 a0001c0002t0001g0039 others(1): Show |
4 | HG02109.hp2 HG02615.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.2427+240C>T | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 14/26 | chr5 | 55276026 | |||||||
| chr5:55276477 | G | C | 5 | a0001c0002t0001g0040 a0001c0002t0001g0041 a0001c0002t0001g0252 others(2): Show |
5 | HG02280.hp1 HG02486.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.2287-71C>G | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 13/26 | chr5 | 55276477 | |||||||
| chr5:55276527 | A | T | 1 | a0001c0002t0001g0037 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2287-121T>A | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 13/26 | chr5 | 55276527 | |||||||
| chr5:55276571 | T | C | 1 | a0001c0001t0001g0098 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2287-165A>G | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 13/26 | chr5 | 55276571 | |||||||
| chr5:55276592 | C | G | 2 | a0001c0001t0001g0022 a0001c0001t0001g0179 |
3 | HG02129.hp1 NA18989.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.2287-186G>C | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 13/26 | chr5 | 55276592 | |||||||
| chr5:55276955 | C | T | 1 | a0001c0001t0001g0052 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2286+151G>A | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 13/26 | chr5 | 55276955 | |||||||
| chr5:55277409 | G | A | 1 | a0003c0005t0001g0055 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2110-127C>T | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 12/26 | chr5 | 55277409 | |||||||
| chr5:55277427 | A | T | 2 | a0002c0004t0004g0042 a0002c0004t0004g0043 |
2 | HG01168.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.2110-145T>A | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 12/26 | chr5 | 55277427 | |||||||
| chr5:55277530 | ACT | A | 58 | a0001c0002t0001g0002 a0001c0002t0001g0004 a0001c0002t0001g0007 others(55): Show |
77 | HG00423.hp2 HG00621.hp2 HG00733.hp2 others(74): Show |
intron_variant | MODIFIER | c.2110-250_2110-249d others(4): Show |
DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 12/26 | chr5 | 55277530 | |||||||
| chr5:55277552 | G | A | 24 | a0001c0001t0001g0021 a0001c0001t0001g0024 a0001c0001t0001g0025 others(21): Show |
27 | HG00423.hp1 HG00597.hp2 HG01081.hp2 others(24): Show |
intron_variant | MODIFIER | c.2110-270C>T | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 12/26 | chr5 | 55277552 | |||||||
| chr5:55277580 | G | T | 6 | a0001c0001t0001g0003 a0001c0001t0001g0116 a0001c0001t0001g0117 others(3): Show |
10 | HG01109.hp2 HG01515.hp2 HG01517.hp2 others(7): Show |
intron_variant | MODIFIER | c.2110-298C>A | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 12/26 | chr5 | 55277580 | |||||||
| chr5:55277695 | C | T | 1 | a0001c0001t0001g0051 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2110-413G>A | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 12/26 | chr5 | 55277695 | |||||||
| chr5:55277727 | G | A | 1 | a0001c0001t0001g0171 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2110-445C>T | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 12/26 | chr5 | 55277727 | |||||||
| chr5:55277905 | C | CA | 11 | a0001c0001t0001g0100 a0001c0001t0001g0124 a0001c0001t0001g0130 others(8): Show |
12 | HG01891.hp2 HG02257.hp1 HG03654.hp1 others(9): Show |
intron_variant | MODIFIER | c.2110-624dupT | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 12/26 | chr5 | 55277905 | |||||||
| chr5:55277905 | CA | C | 70 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(67): Show |
89 | HG00423.hp2 HG00621.hp2 HG00733.hp2 others(86): Show |
intron_variant | MODIFIER | c.2110-624delT | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 12/26 | chr5 | 55277905 | |||||||
| chr5:55277983 | G | A | 1 | a0001c0002t0001g0253 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2110-701C>T | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 12/26 | chr5 | 55277983 | |||||||
| chr5:55278071 | G | A | 29 | a0001c0001t0002g0006 a0001c0001t0002g0010 a0001c0001t0002g0011 others(26): Show |
41 | HG00609.hp1 HG00741.hp1 HG01433.hp1 others(38): Show |
intron_variant | MODIFIER | c.2110-789C>T | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 12/26 | chr5 | 55278071 | |||||||
| chr5:55278079 | C | A | 4 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0132 others(1): Show |
4 | NA18970.hp2 NA18975.hp1 NA19060.hp2 others(1): Show |
intron_variant | MODIFIER | c.2110-797G>T | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 12/26 | chr5 | 55278079 | |||||||
| chr5:55278116 | C | T | 2 | a0002c0004t0004g0042 a0002c0004t0004g0043 |
2 | HG01168.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.2110-834G>A | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 12/26 | chr5 | 55278116 | |||||||
| chr5:55278183 | T | C | 2 | a0001c0001t0001g0050 a0001c0001t0001g0053 |
2 | HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2110-901A>G | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 12/26 | chr5 | 55278183 | |||||||
| chr5:55278223 | C | T | 1 | a0001c0001t0001g0081 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.2110-941G>A | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 12/26 | chr5 | 55278223 | |||||||
| chr5:55278420 | T | C | 2 | a0001c0001t0001g0026 a0001c0001t0001g0173 |
3 | HG00140.hp1 HG06807.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.2110-1138A>G | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 12/26 | chr5 | 55278420 | |||||||
| chr5:55278476 | T | C | 29 | a0001c0001t0002g0006 a0001c0001t0002g0010 a0001c0001t0002g0011 others(26): Show |
41 | HG00609.hp1 HG00741.hp1 HG01433.hp1 others(38): Show |
intron_variant | MODIFIER | c.2110-1194A>G | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 12/26 | chr5 | 55278476 | |||||||
| chr5:55278496 | C | G | 1 | a0001c0001t0001g0163 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2110-1214G>C | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 12/26 | chr5 | 55278496 | |||||||
| chr5:55278639 | C | A | 2 | a0002c0004t0004g0042 a0002c0004t0004g0043 |
2 | HG01168.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.2110-1357G>T | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 12/26 | chr5 | 55278639 | |||||||
| chr5:55278640 | A | T | 2 | a0002c0004t0004g0042 a0002c0004t0004g0043 |
2 | HG01168.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.2110-1358T>A | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 12/26 | chr5 | 55278640 | |||||||
| chr5:55278665 | G | T | 2 | a0001c0001t0001g0019 a0001c0001t0001g0122 |
3 | HG01891.hp1 HG02145.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.2110-1383C>A | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 12/26 | chr5 | 55278665 | |||||||
| chr5:55278702 | G | A | 1 | a0002c0004t0004g0043 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2110-1420C>T | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 12/26 | chr5 | 55278702 | |||||||
| chr5:55278973 | A | C | 1 | a0001c0001t0001g0145 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.2110-1691T>G | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 12/26 | chr5 | 55278973 | |||||||
| chr5:55279164 | G | A | 2 | a0003c0005t0001g0054 a0003c0005t0001g0055 |
2 | HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2110-1882C>T | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 12/26 | chr5 | 55279164 | |||||||
| chr5:55279258 | C | T | 102 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(99): Show |
133 | HG00423.hp2 HG00609.hp1 HG00621.hp2 others(130): Show |
intron_variant | MODIFIER | c.2110-1976G>A | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 12/26 | chr5 | 55279258 | |||||||
| chr5:55279392 | A | AGACT | 73 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(70): Show |
92 | HG00423.hp2 HG00621.hp2 HG00733.hp2 others(89): Show |
intron_variant | MODIFIER | c.2109+1979_2109+198 others(8): Show |
DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 12/26 | chr5 | 55279392 | |||||||
| chr5:55279436 | G | C | 2 | a0002c0004t0004g0042 a0002c0004t0004g0043 |
2 | HG01168.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.2109+1936C>G | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 12/26 | chr5 | 55279436 | |||||||
| chr5:55279478 | A | C | 2 | a0002c0004t0004g0042 a0002c0004t0004g0043 |
2 | HG01168.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.2109+1894T>G | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 12/26 | chr5 | 55279478 | |||||||
| chr5:55279635 | C | T | 2 | a0002c0004t0004g0042 a0002c0004t0004g0043 |
2 | HG01168.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.2109+1737G>A | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 12/26 | chr5 | 55279635 | |||||||
| chr5:55279661 | G | A | 4 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0132 others(1): Show |
4 | NA18970.hp2 NA18975.hp1 NA19060.hp2 others(1): Show |
intron_variant | MODIFIER | c.2109+1711C>T | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 12/26 | chr5 | 55279661 | |||||||
| chr5:55279732 | G | GT | 3 | a0001c0002t0001g0040 a0001c0002t0001g0041 a0001c0002t0001g0252 |
3 | HG02280.hp1 HG02486.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.2109+1639dupA | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 12/26 | chr5 | 55279732 | |||||||
| chr5:55279737 | TG | T | 59 | a0001c0002t0001g0002 a0001c0002t0001g0004 a0001c0002t0001g0007 others(56): Show |
77 | HG00423.hp2 HG00621.hp2 HG00733.hp2 others(74): Show |
intron_variant | MODIFIER | c.2109+1634delC | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 12/26 | chr5 | 55279737 | |||||||
| chr5:55279738 | G | GT | 6 | a0001c0001t0001g0003 a0001c0001t0001g0062 a0001c0001t0001g0067 others(3): Show |
6 | HG01255.hp2 HG01358.hp1 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.2109+1633dupA | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 12/26 | chr5 | 55279738 | |||||||
| chr5:55279738 | G | T | 6 | a0001c0002t0001g0002 a0001c0002t0001g0040 a0001c0002t0001g0041 others(3): Show |
6 | HG02280.hp1 HG02486.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.2109+1634C>A | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 12/26 | chr5 | 55279738 | |||||||
| chr5:55279739 | T | G | 1 | a0001c0001t0001g0102 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2109+1633A>C | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 12/26 | chr5 | 55279739 | |||||||
| chr5:55279761 | G | A | 2 | a0002c0004t0004g0042 a0002c0004t0004g0043 |
2 | HG01168.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.2109+1611C>T | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 12/26 | chr5 | 55279761 | |||||||
| chr5:55279819 | C | G | 1 | a0001c0001t0001g0080 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.2109+1553G>C | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 12/26 | chr5 | 55279819 | |||||||
| chr5:55279847 | T | C | 1 | a0001c0001t0001g0103 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.2109+1525A>G | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 12/26 | chr5 | 55279847 | |||||||
| chr5:55279874 | AT | A | 29 | a0001c0001t0002g0006 a0001c0001t0002g0010 a0001c0001t0002g0011 others(26): Show |
41 | HG00609.hp1 HG00741.hp1 HG01433.hp1 others(38): Show |
intron_variant | MODIFIER | c.2109+1497delA | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 12/26 | chr5 | 55279874 | |||||||
| chr5:55279941 | A | G | 5 | a0001c0002t0001g0040 a0001c0002t0001g0041 a0001c0002t0001g0252 others(2): Show |
5 | HG02280.hp1 HG02486.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.2109+1431T>C | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 12/26 | chr5 | 55279941 | |||||||
| chr5:55280003 | A | G | 1 | a0001c0002t0001g0040 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2109+1369T>C | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 12/26 | chr5 | 55280003 | |||||||
| chr5:55280005 | C | T | 1 | a0001c0001t0001g0079 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2109+1367G>A | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 12/26 | chr5 | 55280005 | |||||||
| chr5:55280112 | G | C | 1 | a0001c0001t0001g0174 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2109+1260C>G | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 12/26 | chr5 | 55280112 | |||||||
| chr5:55280153 | A | G | 1 | a0001c0001t0001g0181 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2109+1219T>C | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 12/26 | chr5 | 55280153 | |||||||
| chr5:55280216 | C | T | 2 | a0002c0004t0004g0042 a0002c0004t0004g0043 |
2 | HG01168.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.2109+1156G>A | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 12/26 | chr5 | 55280216 | |||||||
| chr5:55280400 | T | C | 1 | a0001c0001t0001g0104 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.2109+972A>G | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 12/26 | chr5 | 55280400 | |||||||
| chr5:55280403 | C | G | 1 | a0001c0001t0001g0059 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.2109+969G>C | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 12/26 | chr5 | 55280403 | |||||||
| chr5:55280435 | C | T | 152 | a0001c0001t0001g0005 a0001c0001t0001g0021 a0001c0001t0001g0022 others(149): Show |
192 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(189): Show |
intron_variant | MODIFIER | c.2109+937G>A | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 12/26 | chr5 | 55280435 | |||||||
| chr5:55280474 | T | G | 2 | a0001c0001t0001g0105 a0001c0001t0001g0111 |
2 | HG02074.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.2109+898A>C | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 12/26 | chr5 | 55280474 | |||||||
| chr5:55280485 | T | C | 2 | a0002c0004t0004g0042 a0002c0004t0004g0043 |
2 | HG01168.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.2109+887A>G | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 12/26 | chr5 | 55280485 | |||||||
| chr5:55280751 | C | A | 1 | a0001c0002t0001g0241 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2109+621G>T | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 12/26 | chr5 | 55280751 | |||||||
| chr5:55280811 | G | A | 2 | a0002c0004t0004g0042 a0002c0004t0004g0043 |
2 | HG01168.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.2109+561C>T | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 12/26 | chr5 | 55280811 | |||||||
| chr5:55281062 | TAC | T | 5 | a0001c0001t0001g0064 a0001c0001t0001g0074 a0001c0001t0002g0029 others(2): Show |
6 | HG01891.hp2 HG02257.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.2109+308_2109+309d others(4): Show |
DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 12/26 | chr5 | 55281062 | |||||||
| chr5:55281080 | C | CACACAT | 3 | a0001c0002t0001g0239 a0001c0002t0001g0250 a0001c0002t0001g0251 |
3 | HG00735.hp1 HG02735.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.2109+291_2109+292i others(8): Show |
DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 12/26 | chr5 | 55281080 | |||||||
| chr5:55281080 | C | CACAT | 58 | a0001c0002t0001g0002 a0001c0002t0001g0004 a0001c0002t0001g0007 others(55): Show |
77 | HG00423.hp2 HG00621.hp2 HG00733.hp2 others(74): Show |
intron_variant | MODIFIER | c.2109+291_2109+292i others(6): Show |
DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 12/26 | chr5 | 55281080 | |||||||
| chr5:55281080 | C | CAT | 5 | a0001c0002t0001g0040 a0001c0002t0001g0041 a0001c0002t0001g0252 others(2): Show |
5 | HG02280.hp1 HG02486.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.2109+291_2109+292i others(4): Show |
DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 12/26 | chr5 | 55281080 | |||||||
| chr5:55281081 | G | A | 49 | a0001c0001t0001g0005 a0001c0001t0001g0021 a0001c0001t0001g0022 others(46): Show |
57 | HG00140.hp1 HG00423.hp1 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.2109+291C>T | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 12/26 | chr5 | 55281081 | |||||||
| chr5:55281101 | T | C | 2 | a0002c0004t0004g0042 a0002c0004t0004g0043 |
2 | HG01168.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.2109+271A>G | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 12/26 | chr5 | 55281101 | |||||||
| chr5:55281117 | TAC | T | 56 | a0001c0002t0001g0002 a0001c0002t0001g0004 a0001c0002t0001g0007 others(53): Show |
75 | HG00423.hp2 HG00621.hp2 HG00733.hp2 others(72): Show |
intron_variant | MODIFIER | c.2109+253_2109+254d others(4): Show |
DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 12/26 | chr5 | 55281117 | |||||||
| chr5:55281117 | TACAC | T | 3 | a0001c0001t0001g0059 a0001c0001t0003g0034 a0001c0001t0003g0035 |
3 | NA18950.hp1 NA19064.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.2109+251_2109+254d others(6): Show |
DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 12/26 | chr5 | 55281117 | |||||||
| chr5:55281803 | G | C | 1 | a0001c0002t0001g0252 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1966-288C>G | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 11/26 | chr5 | 55281803 | |||||||
| chr5:55282005 | C | T | 29 | a0001c0001t0002g0006 a0001c0001t0002g0010 a0001c0001t0002g0011 others(26): Show |
41 | HG00609.hp1 HG00741.hp1 HG01433.hp1 others(38): Show |
intron_variant | MODIFIER | c.1966-490G>A | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 11/26 | chr5 | 55282005 | |||||||
| chr5:55282065 | C | T | 54 | a0001c0002t0001g0002 a0001c0002t0001g0004 a0001c0002t0001g0007 others(51): Show |
73 | HG00423.hp2 HG00621.hp2 HG00733.hp2 others(70): Show |
intron_variant | MODIFIER | c.1966-550G>A | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 11/26 | chr5 | 55282065 | |||||||
| chr5:55282583 | A | C | 1 | a0001c0007t0001g0256 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1965+620T>G | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 11/26 | chr5 | 55282583 | |||||||
| chr5:55282642 | T | G | 1 | a0001c0001t0001g0109 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1965+561A>C | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 11/26 | chr5 | 55282642 | |||||||
| chr5:55282659 | C | T | 1 | a0001c0001t0001g0153 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1965+544G>A | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 11/26 | chr5 | 55282659 | |||||||
| chr5:55282714 | T | C | 1 | a0001c0002t0001g0252 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1965+489A>G | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 11/26 | chr5 | 55282714 | |||||||
| chr5:55282762 | G | T | 2 | a0002c0004t0004g0042 a0002c0004t0004g0043 |
2 | HG01168.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1965+441C>A | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 11/26 | chr5 | 55282762 | |||||||
| chr5:55282881 | T | A | 1 | a0001c0001t0001g0183 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1965+322A>T | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 11/26 | chr5 | 55282881 | |||||||
| chr5:55284086 | T | C | 66 | a0001c0001t0001g0133 a0001c0002t0001g0002 a0001c0002t0001g0004 others(63): Show |
85 | HG00423.hp2 HG00621.hp2 HG00733.hp2 others(82): Show |
intron_variant | MODIFIER | c.1357-275A>G | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 10/26 | chr5 | 55284086 | |||||||
| chr5:55284479 | G | T | 2 | a0002c0004t0004g0042 a0002c0004t0004g0043 |
2 | HG01168.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1357-668C>A | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 10/26 | chr5 | 55284479 | |||||||
| chr5:55284596 | G | A | 1 | a0001c0001t0001g0106 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1356+697C>T | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 10/26 | chr5 | 55284596 | |||||||
| chr5:55284927 | G | A | 29 | a0001c0001t0002g0006 a0001c0001t0002g0010 a0001c0001t0002g0011 others(26): Show |
41 | HG00609.hp1 HG00741.hp1 HG01433.hp1 others(38): Show |
intron_variant | MODIFIER | c.1356+366C>T | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 10/26 | chr5 | 55284927 | |||||||
| chr5:55285140 | C | A | 2 | a0002c0004t0004g0042 a0002c0004t0004g0043 |
2 | HG01168.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1356+153G>T | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 10/26 | chr5 | 55285140 | |||||||
| chr5:55285226 | A | G | 2 | a0001c0001t0001g0046 a0001c0001t0001g0125 |
2 | HG02129.hp2 NA18957.hp2 |
intron_variant | MODIFIER | c.1356+67T>C | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 10/26 | chr5 | 55285226 | |||||||
| chr5:55285914 | T | C | 1 | a0001c0002t0001g0255 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1067-53A>G | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 8/26 | chr5 | 55285914 | |||||||
| chr5:55286111 | C | T | 1 | a0001c0001t0001g0181 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1067-250G>A | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 8/26 | chr5 | 55286111 | |||||||
| chr5:55286114 | C | T | 4 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0144 others(1): Show |
4 | HG00140.hp2 HG01081.hp1 NA20752.hp1 others(1): Show |
intron_variant | MODIFIER | c.1067-253G>A | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 8/26 | chr5 | 55286114 | |||||||
| chr5:55286128 | C | T | 1 | a0001c0001t0002g0191 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1067-267G>A | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 8/26 | chr5 | 55286128 | |||||||
| chr5:55286140 | G | A | 2 | a0002c0004t0004g0042 a0002c0004t0004g0043 |
2 | HG01168.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1067-279C>T | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 8/26 | chr5 | 55286140 | |||||||
| chr5:55286435 | A | C | 60 | a0001c0002t0001g0002 a0001c0002t0001g0004 a0001c0002t0001g0007 others(57): Show |
79 | HG00423.hp2 HG00621.hp2 HG00733.hp2 others(76): Show |
intron_variant | MODIFIER | c.1067-574T>G | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 8/26 | chr5 | 55286435 | |||||||
| chr5:55287024 | T | C | 2 | a0003c0005t0001g0054 a0003c0005t0001g0055 |
2 | HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1067-1163A>G | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 8/26 | chr5 | 55287024 | |||||||
| chr5:55287157 | T | C | 60 | a0001c0002t0001g0002 a0001c0002t0001g0004 a0001c0002t0001g0007 others(57): Show |
79 | HG00423.hp2 HG00621.hp2 HG00733.hp2 others(76): Show |
intron_variant | MODIFIER | c.1067-1296A>G | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 8/26 | chr5 | 55287157 | |||||||
| chr5:55287297 | C | T | 1 | a0001c0001t0001g0162 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1067-1436G>A | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 8/26 | chr5 | 55287297 | |||||||
| chr5:55287588 | T | A | 2 | a0002c0004t0004g0042 a0002c0004t0004g0043 |
2 | HG01168.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1066+1682A>T | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 8/26 | chr5 | 55287588 | |||||||
| chr5:55287589 | T | A | 6 | a0001c0001t0001g0147 a0001c0001t0001g0175 a0001c0001t0001g0176 others(3): Show |
6 | HG01123.hp1 HG01168.hp2 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.1066+1681A>T | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 8/26 | chr5 | 55287589 | |||||||
| chr5:55287604 | C | A | 2 | a0002c0004t0004g0042 a0002c0004t0004g0043 |
2 | HG01168.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1066+1666G>T | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 8/26 | chr5 | 55287604 | |||||||
| chr5:55287677 | G | A | 2 | a0001c0001t0002g0027 a0001c0001t0002g0187 |
3 | HG02818.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1066+1593C>T | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 8/26 | chr5 | 55287677 | |||||||
| chr5:55287898 | G | A | 1 | a0001c0002t0001g0252 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1066+1372C>T | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 8/26 | chr5 | 55287898 | |||||||
| chr5:55287938 | G | T | 3 | a0001c0002t0001g0037 a0001c0002t0001g0038 a0001c0002t0001g0039 |
3 | HG02109.hp2 HG02615.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1066+1332C>A | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 8/26 | chr5 | 55287938 | |||||||
| chr5:55287951 | A | G | 1 | a0001c0001t0001g0048 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1066+1319T>C | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 8/26 | chr5 | 55287951 | |||||||
| chr5:55288386 | T | C | 1 | a0001c0002t0001g0013 | 3 | NA18948.hp2 NA18960.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.1066+884A>G | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 8/26 | chr5 | 55288386 | |||||||
| chr5:55288468 | A | T | 1 | a0001c0002t0001g0222 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1066+802T>A | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 8/26 | chr5 | 55288468 | |||||||
| chr5:55288657 | A | T | 1 | a0001c0001t0001g0075 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1066+613T>A | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 8/26 | chr5 | 55288657 | |||||||
| chr5:55288678 | G | A | 5 | a0001c0001t0002g0012 a0001c0001t0002g0203 a0001c0001t0002g0204 others(2): Show |
7 | HG00741.hp1 HG01433.hp1 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.1066+592C>T | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 8/26 | chr5 | 55288678 | |||||||
| chr5:55288687 | A | G | 60 | a0001c0002t0001g0002 a0001c0002t0001g0004 a0001c0002t0001g0007 others(57): Show |
79 | HG00423.hp2 HG00621.hp2 HG00733.hp2 others(76): Show |
intron_variant | MODIFIER | c.1066+583T>C | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 8/26 | chr5 | 55288687 | |||||||
| chr5:55288786 | A | C | 1 | a0001c0002t0001g0221 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1066+484T>G | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 8/26 | chr5 | 55288786 | |||||||
| chr5:55289104 | G | A | 2 | a0002c0004t0004g0042 a0002c0004t0004g0043 |
2 | HG01168.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1066+166C>T | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 8/26 | chr5 | 55289104 | |||||||
| chr5:55289170 | G | A | 5 | a0001c0002t0001g0040 a0001c0002t0001g0041 a0001c0002t0001g0252 others(2): Show |
5 | HG02280.hp1 HG02486.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1066+100C>T | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 8/26 | chr5 | 55289170 | |||||||
| chr5:55289442 | A | T | 1 | a0009c0016t0001g0259 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.908-14T>A | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 7/26 | chr5 | 55289442 | |||||||
| chr5:55289616 | G | A | 7 | a0001c0002t0001g0033 a0001c0002t0001g0242 a0001c0002t0001g0244 others(4): Show |
8 | HG01167.hp1 HG02451.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.908-188C>T | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 7/26 | chr5 | 55289616 | |||||||
| chr5:55289681 | A | T | 1 | a0001c0002t0001g0220 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.908-253T>A | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 7/26 | chr5 | 55289681 | |||||||
| chr5:55290887 | T | C | 73 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(70): Show |
92 | HG00423.hp2 HG00621.hp2 HG00733.hp2 others(89): Show |
intron_variant | MODIFIER | c.781-543A>G | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 6/26 | chr5 | 55290887 | |||||||
| chr5:55290892 | A | G | 2 | a0002c0004t0004g0042 a0002c0004t0004g0043 |
2 | HG01168.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.781-548T>C | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 6/26 | chr5 | 55290892 | |||||||
| chr5:55290950 | G | A | 4 | a0001c0002t0001g0007 a0001c0002t0001g0234 a0001c0002t0001g0235 others(1): Show |
7 | NA18747.hp2 NA18957.hp1 NA18962.hp1 others(4): Show |
intron_variant | MODIFIER | c.781-606C>T | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 6/26 | chr5 | 55290950 | |||||||
| chr5:55291057 | T | A | 1 | a0001c0001t0001g0107 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.781-713A>T | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 6/26 | chr5 | 55291057 | |||||||
| chr5:55291757 | G | T | 7 | a0001c0001t0001g0021 a0001c0001t0001g0145 a0001c0001t0001g0148 others(4): Show |
8 | HG00597.hp2 HG02027.hp2 HG02132.hp2 others(5): Show |
intron_variant | MODIFIER | c.781-1413C>A | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 6/26 | chr5 | 55291757 | |||||||
| chr5:55291789 | T | C | 2 | a0002c0004t0004g0042 a0002c0004t0004g0043 |
2 | HG01168.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.781-1445A>G | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 6/26 | chr5 | 55291789 | |||||||
| chr5:55291830 | G | A | 1 | a0001c0001t0001g0108 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.781-1486C>T | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 6/26 | chr5 | 55291830 | |||||||
| chr5:55291955 | G | C | 1 | a0001c0001t0001g0128 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.781-1611C>G | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 6/26 | chr5 | 55291955 | |||||||
| chr5:55292311 | T | C | 3 | a0001c0001t0002g0010 a0001c0001t0002g0190 a0001c0001t0002g0193 |
5 | HG02280.hp2 HG03516.hp1 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.780+1706A>G | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 6/26 | chr5 | 55292311 | |||||||
| chr5:55292354 | C | T | 2 | a0001c0001t0001g0064 a0001c0001t0001g0074 |
2 | HG02572.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.780+1663G>A | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 6/26 | chr5 | 55292354 | |||||||
| chr5:55292433 | T | C | 29 | a0001c0001t0002g0006 a0001c0001t0002g0010 a0001c0001t0002g0011 others(26): Show |
41 | HG00609.hp1 HG00741.hp1 HG01433.hp1 others(38): Show |
intron_variant | MODIFIER | c.780+1584A>G | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 6/26 | chr5 | 55292433 | |||||||
| chr5:55292676 | C | T | 1 | a0001c0001t0001g0157 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.780+1341G>A | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 6/26 | chr5 | 55292676 | |||||||
| chr5:55292831 | A | C | 1 | a0001c0001t0001g0177 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.780+1186T>G | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 6/26 | chr5 | 55292831 | |||||||
| chr5:55292996 | TA | T | 50 | a0001c0001t0001g0005 a0001c0001t0001g0021 a0001c0001t0001g0022 others(47): Show |
59 | HG00140.hp1 HG00423.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.780+1020delT | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 6/26 | chr5 | 55292996 | |||||||
| chr5:55293088 | G | A | 1 | a0001c0001t0002g0192 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.780+929C>T | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 6/26 | chr5 | 55293088 | |||||||
| chr5:55293303 | T | C | 1 | a0001c0001t0001g0109 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.780+714A>G | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 6/26 | chr5 | 55293303 | |||||||
| chr5:55293515 | T | C | 5 | a0001c0002t0001g0040 a0001c0002t0001g0041 a0001c0002t0001g0252 others(2): Show |
5 | HG02280.hp1 HG02486.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.780+502A>G | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 6/26 | chr5 | 55293515 | |||||||
| chr5:55293526 | CTAATT | C | 6 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(3): Show |
6 | HG01243.hp1 HG03041.hp2 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.780+486_780+490del others(5): Show |
DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 6/26 | chr5 | 55293526 | |||||||
| chr5:55293705 | A | G | 6 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(3): Show |
6 | HG01243.hp1 HG03041.hp2 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.780+312T>C | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 6/26 | chr5 | 55293705 | |||||||
| chr5:55294000 | C | T | 8 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(5): Show |
8 | HG01168.hp2 HG01243.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.780+17G>A | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 6/26 | chr5 | 55294000 | |||||||
| chr5:55294238 | A | C | 1 | a0001c0001t0001g0073 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.652-93T>G | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 5/26 | chr5 | 55294238 | |||||||
| chr5:55294441 | A | G | 73 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(70): Show |
92 | HG00423.hp2 HG00621.hp2 HG00733.hp2 others(89): Show |
intron_variant | MODIFIER | c.652-296T>C | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 5/26 | chr5 | 55294441 | |||||||
| chr5:55294446 | G | A | 2 | a0002c0004t0004g0042 a0002c0004t0004g0043 |
2 | HG01168.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.652-301C>T | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 5/26 | chr5 | 55294446 | |||||||
| chr5:55294583 | G | A | 1 | a0001c0001t0001g0143 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.652-438C>T | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 5/26 | chr5 | 55294583 | |||||||
| chr5:55294589 | G | A | 2 | a0002c0004t0004g0042 a0002c0004t0004g0043 |
2 | HG01168.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.652-444C>T | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 5/26 | chr5 | 55294589 | |||||||
| chr5:55294627 | T | A | 2 | a0002c0004t0004g0042 a0002c0004t0004g0043 |
2 | HG01168.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.652-482A>T | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 5/26 | chr5 | 55294627 | |||||||
| chr5:55294628 | G | T | 2 | a0002c0004t0004g0042 a0002c0004t0004g0043 |
2 | HG01168.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.652-483C>A | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 5/26 | chr5 | 55294628 | |||||||
| chr5:55294629 | A | C | 2 | a0002c0004t0004g0042 a0002c0004t0004g0043 |
2 | HG01168.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.652-484T>G | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 5/26 | chr5 | 55294629 | |||||||
| chr5:55294656 | G | A | 1 | a0001c0001t0001g0110 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.652-511C>T | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 5/26 | chr5 | 55294656 | |||||||
| chr5:55294658 | A | G | 152 | a0001c0001t0001g0005 a0001c0001t0001g0021 a0001c0001t0001g0022 others(149): Show |
192 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(189): Show |
intron_variant | MODIFIER | c.652-513T>C | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 5/26 | chr5 | 55294658 | |||||||
| chr5:55294889 | G | A | 2 | a0001c0002t0001g0210 a0001c0002t0001g0243 |
2 | HG02809.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.651+490C>T | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 5/26 | chr5 | 55294889 | |||||||
| chr5:55294920 | G | A | 1 | a0001c0001t0001g0051 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.651+459C>T | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 5/26 | chr5 | 55294920 | |||||||
| chr5:55294979 | G | A | 2 | a0002c0004t0004g0042 a0002c0004t0004g0043 |
2 | HG01168.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.651+400C>T | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 5/26 | chr5 | 55294979 | |||||||
| chr5:55294997 | T | C | 6 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(3): Show |
6 | HG01243.hp1 HG03041.hp2 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.651+382A>G | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 5/26 | chr5 | 55294997 | |||||||
| chr5:55295155 | C | G | 6 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(3): Show |
6 | HG01243.hp1 HG03041.hp2 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.651+224G>C | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 5/26 | chr5 | 55295155 | |||||||
| chr5:55295209 | A | G | 2 | a0002c0004t0004g0042 a0002c0004t0004g0043 |
2 | HG01168.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.651+170T>C | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 5/26 | chr5 | 55295209 | |||||||
| chr5:55295568 | T | C | 1 | a0001c0001t0001g0111 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.506-44A>G | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 4/26 | chr5 | 55295568 | |||||||
| chr5:55295716 | T | C | 1 | a0001c0002t0001g0236 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.506-192A>G | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 4/26 | chr5 | 55295716 | |||||||
| chr5:55296162 | A | G | 1 | a0001c0001t0002g0028 | 2 | HG02809.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.505+58T>C | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 4/26 | chr5 | 55296162 | |||||||
| chr5:55296648 | A | G | 2 | a0001c0001t0001g0148 a0001c0001t0001g0180 |
2 | NA18949.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.376-299T>C | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 3/26 | chr5 | 55296648 | |||||||
| chr5:55296671 | T | C | 2 | a0001c0001t0001g0148 a0001c0001t0001g0180 |
2 | NA18949.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.376-322A>G | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 3/26 | chr5 | 55296671 | |||||||
| chr5:55296721 | G | C | 1 | a0001c0001t0001g0058 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.376-372C>G | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 3/26 | chr5 | 55296721 | |||||||
| chr5:55296735 | GATTTA | G | 5 | a0001c0002t0001g0040 a0001c0002t0001g0041 a0001c0002t0001g0252 others(2): Show |
5 | HG02280.hp1 HG02486.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.376-391_376-387del others(5): Show |
DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 3/26 | chr5 | 55296735 | |||||||
| chr5:55297188 | T | A | 60 | a0001c0002t0001g0002 a0001c0002t0001g0004 a0001c0002t0001g0007 others(57): Show |
79 | HG00423.hp2 HG00621.hp2 HG00733.hp2 others(76): Show |
intron_variant | MODIFIER | c.375+97A>T | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 3/26 | chr5 | 55297188 | |||||||
| chr5:55297274 | T | C | 1 | a0001c0002t0001g0249 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.375+11A>G | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 3/26 | chr5 | 55297274 | |||||||
| chr5:55297417 | T | A | 1 | a0001c0001t0002g0207 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.262-19A>T | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 2/26 | chr5 | 55297417 | |||||||
| chr5:55297419 | A | G | 5 | a0001c0002t0001g0040 a0001c0002t0001g0041 a0001c0002t0001g0252 others(2): Show |
5 | HG02280.hp1 HG02486.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.262-21T>C | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 2/26 | chr5 | 55297419 | |||||||
| chr5:55297794 | C | T | 1 | a0001c0001t0001g0051 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.262-396G>A | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 2/26 | chr5 | 55297794 | |||||||
| chr5:55297830 | G | A | 2 | a0001c0002t0001g0250 a0001c0002t0001g0251 |
2 | HG02735.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.262-432C>T | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 2/26 | chr5 | 55297830 | |||||||
| chr5:55298142 | T | C | 1 | a0001c0002t0001g0237 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.261+449A>G | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 2/26 | chr5 | 55298142 | |||||||
| chr5:55298300 | G | A | 5 | a0001c0002t0001g0040 a0001c0002t0001g0041 a0001c0002t0001g0252 others(2): Show |
5 | HG02280.hp1 HG02486.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.261+291C>T | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 2/26 | chr5 | 55298300 | |||||||
| chr5:55298339 | T | C | 2 | a0001c0001t0001g0067 a0001c0001t0001g0068 |
2 | HG01255.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.261+252A>G | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 2/26 | chr5 | 55298339 | |||||||
| chr5:55298446 | T | G | 6 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(3): Show |
6 | HG01243.hp1 HG03041.hp2 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.261+145A>C | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 2/26 | chr5 | 55298446 | |||||||
| chr5:55298457 | G | A | 52 | a0001c0002t0001g0002 a0001c0002t0001g0004 a0001c0002t0001g0007 others(49): Show |
71 | HG00423.hp2 HG00621.hp2 HG00733.hp2 others(68): Show |
intron_variant | MODIFIER | c.261+134C>T | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 2/26 | chr5 | 55298457 | |||||||
| chr5:55298678 | T | C | 2 | a0002c0004t0004g0042 a0002c0004t0004g0043 |
2 | HG01168.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.188-14A>G | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 1/26 | chr5 | 55298678 | |||||||
| chr5:55298697 | A | G | 1 | a0001c0001t0001g0159 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.188-33T>C | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 1/26 | chr5 | 55298697 | |||||||
| chr5:55298899 | G | A | 60 | a0001c0002t0001g0002 a0001c0002t0001g0004 a0001c0002t0001g0007 others(57): Show |
79 | HG00423.hp2 HG00621.hp2 HG00733.hp2 others(76): Show |
intron_variant | MODIFIER | c.188-235C>T | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 1/26 | chr5 | 55298899 | |||||||
| chr5:55298940 | G | A | 1 | a0001c0001t0001g0115 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.188-276C>T | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 1/26 | chr5 | 55298940 | |||||||
| chr5:55298979 | G | A | 65 | a0001c0002t0001g0002 a0001c0002t0001g0004 a0001c0002t0001g0007 others(62): Show |
84 | HG00423.hp2 HG00621.hp2 HG00733.hp2 others(81): Show |
intron_variant | MODIFIER | c.188-315C>T | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 1/26 | chr5 | 55298979 | |||||||
| chr5:55299020 | G | C | 1 | a0001c0001t0001g0129 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.188-356C>G | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 1/26 | chr5 | 55299020 | |||||||
| chr5:55299034 | C | T | 1 | a0001c0001t0001g0070 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.188-370G>A | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 1/26 | chr5 | 55299034 | |||||||
| chr5:55299036 | C | CA | 10 | a0001c0001t0001g0016 a0001c0001t0001g0059 a0001c0001t0001g0063 others(7): Show |
11 | HG00642.hp2 HG01109.hp1 HG01168.hp1 others(8): Show |
intron_variant | MODIFIER | c.188-373dupT | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 1/26 | chr5 | 55299036 | |||||||
| chr5:55299036 | CA | C | 86 | a0001c0001t0001g0005 a0001c0001t0001g0021 a0001c0001t0001g0022 others(83): Show |
107 | HG00140.hp1 HG00423.hp1 HG00597.hp2 others(104): Show |
intron_variant | MODIFIER | c.188-373delT | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 1/26 | chr5 | 55299036 | |||||||
| chr5:55299036 | CAAA | C | 55 | a0001c0002t0001g0002 a0001c0002t0001g0004 a0001c0002t0001g0007 others(52): Show |
72 | HG00423.hp2 HG00621.hp2 HG00733.hp2 others(69): Show |
intron_variant | MODIFIER | c.188-375_188-373del others(3): Show |
DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 1/26 | chr5 | 55299036 | |||||||
| chr5:55299036 | CAAAA | C | 7 | a0001c0002t0001g0013 a0001c0002t0001g0213 a0001c0002t0001g0214 others(4): Show |
9 | HG01167.hp1 HG01168.hp2 HG01256.hp1 others(6): Show |
intron_variant | MODIFIER | c.188-376_188-373del others(4): Show |
DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 1/26 | chr5 | 55299036 | |||||||
| chr5:55299110 | C | T | 6 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(3): Show |
6 | HG01243.hp1 HG03041.hp2 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.188-446G>A | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 1/26 | chr5 | 55299110 | |||||||
| chr5:55299367 | G | A | 29 | a0001c0001t0002g0006 a0001c0001t0002g0010 a0001c0001t0002g0011 others(26): Show |
41 | HG00609.hp1 HG00741.hp1 HG01433.hp1 others(38): Show |
intron_variant | MODIFIER | c.188-703C>T | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 1/26 | chr5 | 55299367 | |||||||
| chr5:55299385 | G | C | 1 | a0001c0001t0001g0046 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.188-721C>G | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 1/26 | chr5 | 55299385 | |||||||
| chr5:55299413 | C | T | 1 | a0001c0001t0001g0158 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.188-749G>A | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 1/26 | chr5 | 55299413 | |||||||
| chr5:55299549 | A | G | 1 | a0001c0001t0001g0069 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.188-885T>C | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 1/26 | chr5 | 55299549 | |||||||
| chr5:55299579 | A | G | 2 | a0002c0004t0004g0042 a0002c0004t0004g0043 |
2 | HG01168.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.188-915T>C | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 1/26 | chr5 | 55299579 | |||||||
| chr5:55299814 | G | A | 60 | a0001c0002t0001g0002 a0001c0002t0001g0004 a0001c0002t0001g0007 others(57): Show |
79 | HG00423.hp2 HG00621.hp2 HG00733.hp2 others(76): Show |
intron_variant | MODIFIER | c.188-1150C>T | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 1/26 | chr5 | 55299814 | |||||||
| chr5:55299939 | C | T | 29 | a0001c0001t0002g0006 a0001c0001t0002g0010 a0001c0001t0002g0011 others(26): Show |
41 | HG00609.hp1 HG00741.hp1 HG01433.hp1 others(38): Show |
intron_variant | MODIFIER | c.188-1275G>A | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 1/26 | chr5 | 55299939 | |||||||
| chr5:55300031 | G | A | 6 | a0001c0001t0001g0003 a0001c0001t0001g0116 a0001c0001t0001g0117 others(3): Show |
10 | HG01109.hp2 HG01515.hp2 HG01517.hp2 others(7): Show |
intron_variant | MODIFIER | c.188-1367C>T | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 1/26 | chr5 | 55300031 | |||||||
| chr5:55300032 | T | C | 2 | a0002c0004t0004g0042 a0002c0004t0004g0043 |
2 | HG01168.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.188-1368A>G | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 1/26 | chr5 | 55300032 | |||||||
| chr5:55300130 | G | C | 3 | a0001c0001t0002g0027 a0001c0001t0002g0187 a0001c0001t0002g0188 |
4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.188-1466C>G | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 1/26 | chr5 | 55300130 | |||||||
| chr5:55300174 | G | C | 2 | a0002c0004t0004g0042 a0002c0004t0004g0043 |
2 | HG01168.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.188-1510C>G | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 1/26 | chr5 | 55300174 | |||||||
| chr5:55300321 | G | A | 1 | a0001c0001t0001g0120 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.188-1657C>T | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 1/26 | chr5 | 55300321 | |||||||
| chr5:55300437 | C | T | 2 | a0001c0001t0001g0051 a0001c0001t0001g0052 |
2 | HG01243.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.188-1773G>A | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 1/26 | chr5 | 55300437 | |||||||
| chr5:55300563 | C | T | 65 | a0001c0002t0001g0002 a0001c0002t0001g0004 a0001c0002t0001g0007 others(62): Show |
84 | HG00423.hp2 HG00621.hp2 HG00733.hp2 others(81): Show |
intron_variant | MODIFIER | c.188-1899G>A | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 1/26 | chr5 | 55300563 | |||||||
| chr5:55300577 | G | C | 1 | a0001c0001t0001g0017 | 2 | HG01099.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.188-1913C>G | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 1/26 | chr5 | 55300577 | |||||||
| chr5:55300878 | T | G | 1 | a0001c0002t0001g0255 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.188-2214A>C | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 1/26 | chr5 | 55300878 | |||||||
| chr5:55300932 | G | T | 160 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0020 others(157): Show |
203 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(200): Show |
intron_variant | MODIFIER | c.188-2268C>A | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 1/26 | chr5 | 55300932 | |||||||
| chr5:55300939 | C | T | 2 | a0002c0004t0004g0042 a0002c0004t0004g0043 |
2 | HG01168.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.188-2275G>A | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 1/26 | chr5 | 55300939 | |||||||
| chr5:55300970 | T | C | 2 | a0002c0004t0004g0042 a0002c0004t0004g0043 |
2 | HG01168.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.188-2306A>G | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 1/26 | chr5 | 55300970 | |||||||
| chr5:55301004 | T | C | 1 | a0001c0001t0001g0126 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.188-2340A>G | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 1/26 | chr5 | 55301004 | |||||||
| chr5:55301039 | T | C | 73 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(70): Show |
92 | HG00423.hp2 HG00621.hp2 HG00733.hp2 others(89): Show |
intron_variant | MODIFIER | c.188-2375A>G | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 1/26 | chr5 | 55301039 | |||||||
| chr5:55301234 | C | T | 2 | a0002c0004t0004g0042 a0002c0004t0004g0043 |
2 | HG01168.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.188-2570G>A | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 1/26 | chr5 | 55301234 | |||||||
| chr5:55301249 | C | T | 2 | a0002c0004t0004g0042 a0002c0004t0004g0043 |
2 | HG01168.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.188-2585G>A | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 1/26 | chr5 | 55301249 | |||||||
| chr5:55301478 | C | T | 1 | a0001c0001t0001g0157 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.188-2814G>A | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 1/26 | chr5 | 55301478 | |||||||
| chr5:55301500 | G | C | 60 | a0001c0002t0001g0002 a0001c0002t0001g0004 a0001c0002t0001g0007 others(57): Show |
79 | HG00423.hp2 HG00621.hp2 HG00733.hp2 others(76): Show |
intron_variant | MODIFIER | c.188-2836C>G | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 1/26 | chr5 | 55301500 | |||||||
| chr5:55301606 | G | A | 29 | a0001c0001t0002g0006 a0001c0001t0002g0010 a0001c0001t0002g0011 others(26): Show |
41 | HG00609.hp1 HG00741.hp1 HG01433.hp1 others(38): Show |
intron_variant | MODIFIER | c.188-2942C>T | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 1/26 | chr5 | 55301606 | |||||||
| chr5:55301628 | G | A | 2 | a0002c0004t0004g0042 a0002c0004t0004g0043 |
2 | HG01168.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.188-2964C>T | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 1/26 | chr5 | 55301628 | |||||||
| chr5:55301713 | C | CA | 13 | a0001c0001t0001g0018 a0001c0001t0001g0060 a0001c0001t0001g0122 others(10): Show |
14 | HG00735.hp2 HG02886.hp1 HG02896.hp2 others(11): Show |
intron_variant | MODIFIER | c.188-3050dupT | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 1/26 | chr5 | 55301713 | |||||||
| chr5:55301713 | C | CAA | 9 | a0001c0001t0001g0019 a0001c0001t0001g0051 a0001c0001t0001g0052 others(6): Show |
10 | HG01243.hp1 HG01891.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.188-3051_188-3050d others(4): Show |
DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 1/26 | chr5 | 55301713 | |||||||
| chr5:55301713 | C | CAAAAAAA others(10): Show |
2 | a0002c0004t0004g0042 a0002c0004t0004g0043 |
2 | HG01168.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.188-3066_188-3050d others(19): Show |
DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 1/26 | chr5 | 55301713 | |||||||
| chr5:55301713 | CA | C | 83 | a0001c0001t0001g0005 a0001c0001t0001g0021 a0001c0001t0001g0022 others(80): Show |
106 | HG00140.hp1 HG00423.hp1 HG00597.hp2 others(103): Show |
intron_variant | MODIFIER | c.188-3050delT | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 1/26 | chr5 | 55301713 | |||||||
| chr5:55301713 | CAA | C | 52 | a0001c0001t0001g0156 a0001c0001t0002g0187 a0001c0002t0001g0002 others(49): Show |
69 | HG00423.hp2 HG00621.hp2 HG00733.hp2 others(66): Show |
intron_variant | MODIFIER | c.188-3051_188-3050d others(4): Show |
DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 1/26 | chr5 | 55301713 | |||||||
| chr5:55301726 | A | C | 1 | a0001c0002t0001g0212 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.188-3062T>G | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 1/26 | chr5 | 55301726 | |||||||
| chr5:55301736 | A | C | 1 | a0001c0002t0001g0211 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.188-3072T>G | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 1/26 | chr5 | 55301736 | |||||||
| chr5:55301737 | C | A | 5 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(2): Show |
5 | HG01243.hp1 HG03041.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.188-3073G>T | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 1/26 | chr5 | 55301737 | |||||||
| chr5:55301768 | G | A | 2 | a0001c0002t0001g0040 a0001c0002t0001g0041 |
2 | HG02486.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.188-3104C>T | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 1/26 | chr5 | 55301768 | |||||||
| chr5:55301829 | T | C | 4 | a0001c0002t0001g0254 a0001c0002t0001g0257 a0001c0002t0001g0258 others(1): Show |
4 | HG02145.hp2 HG02922.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.188-3165A>G | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 1/26 | chr5 | 55301829 | |||||||
| chr5:55301968 | T | C | 60 | a0001c0002t0001g0002 a0001c0002t0001g0004 a0001c0002t0001g0007 others(57): Show |
79 | HG00423.hp2 HG00621.hp2 HG00733.hp2 others(76): Show |
intron_variant | MODIFIER | c.188-3304A>G | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 1/26 | chr5 | 55301968 | |||||||
| chr5:55302153 | T | C | 1 | a0001c0001t0001g0053 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.188-3489A>G | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 1/26 | chr5 | 55302153 | |||||||
| chr5:55302351 | C | A | 2 | a0003c0005t0001g0054 a0003c0005t0001g0055 |
2 | HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.188-3687G>T | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 1/26 | chr5 | 55302351 | |||||||
| chr5:55302512 | T | C | 2 | a0002c0004t0004g0042 a0002c0004t0004g0043 |
2 | HG01168.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.188-3848A>G | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 1/26 | chr5 | 55302512 | |||||||
| chr5:55302556 | A | G | 2 | a0002c0004t0004g0042 a0002c0004t0004g0043 |
2 | HG01168.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.188-3892T>C | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 1/26 | chr5 | 55302556 | |||||||
| chr5:55302563 | T | C | 2 | a0002c0004t0004g0042 a0002c0004t0004g0043 |
2 | HG01168.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.188-3899A>G | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 1/26 | chr5 | 55302563 | |||||||
| chr5:55302582 | G | A | 2 | a0001c0001t0001g0046 a0001c0001t0001g0125 |
2 | HG02129.hp2 NA18957.hp2 |
intron_variant | MODIFIER | c.188-3918C>T | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 1/26 | chr5 | 55302582 | |||||||
| chr5:55302592 | C | CA | 18 | a0001c0001t0001g0126 a0001c0001t0001g0127 a0001c0001t0001g0128 others(15): Show |
19 | HG01358.hp2 HG01433.hp2 HG02027.hp1 others(16): Show |
intron_variant | MODIFIER | c.188-3929dupT | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 1/26 | chr5 | 55302592 | |||||||
| chr5:55302592 | CA | C | 49 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(46): Show |
66 | HG00423.hp2 HG00621.hp2 HG00733.hp2 others(63): Show |
intron_variant | MODIFIER | c.188-3929delT | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 1/26 | chr5 | 55302592 | |||||||
| chr5:55302860 | T | C | 60 | a0001c0002t0001g0002 a0001c0002t0001g0004 a0001c0002t0001g0007 others(57): Show |
79 | HG00423.hp2 HG00621.hp2 HG00733.hp2 others(76): Show |
intron_variant | MODIFIER | c.188-4196A>G | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 1/26 | chr5 | 55302860 | |||||||
| chr5:55302983 | T | C | 2 | a0002c0004t0004g0042 a0002c0004t0004g0043 |
2 | HG01168.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.188-4319A>G | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 1/26 | chr5 | 55302983 | |||||||
| chr5:55303109 | T | TA | 29 | a0001c0001t0001g0133 a0001c0001t0002g0006 a0001c0001t0002g0010 others(26): Show |
41 | HG00609.hp1 HG00741.hp1 HG01071.hp1 others(38): Show |
intron_variant | MODIFIER | c.187+4277dupT | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 1/26 | chr5 | 55303109 | |||||||
| chr5:55303435 | G | C | 29 | a0001c0001t0002g0006 a0001c0001t0002g0010 a0001c0001t0002g0011 others(26): Show |
41 | HG00609.hp1 HG00741.hp1 HG01433.hp1 others(38): Show |
intron_variant | MODIFIER | c.187+3952C>G | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 1/26 | chr5 | 55303435 | |||||||
| chr5:55303520 | G | A | 2 | a0002c0004t0004g0042 a0002c0004t0004g0043 |
2 | HG01168.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.187+3867C>T | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 1/26 | chr5 | 55303520 | |||||||
| chr5:55303676 | T | A | 5 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0136 others(2): Show |
5 | HG02523.hp2 NA18941.hp2 NA19005.hp2 others(2): Show |
intron_variant | MODIFIER | c.187+3711A>T | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 1/26 | chr5 | 55303676 | |||||||
| chr5:55303722 | G | C | 1 | a0001c0002t0001g0250 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.187+3665C>G | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 1/26 | chr5 | 55303722 | |||||||
| chr5:55303806 | T | C | 1 | a0001c0001t0001g0183 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.187+3581A>G | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 1/26 | chr5 | 55303806 | |||||||
| chr5:55303808 | G | C | 18 | a0001c0001t0002g0006 a0001c0001t0002g0011 a0001c0001t0002g0012 others(15): Show |
25 | HG00609.hp1 HG00741.hp1 HG01433.hp1 others(22): Show |
intron_variant | MODIFIER | c.187+3579C>G | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 1/26 | chr5 | 55303808 | |||||||
| chr5:55303949 | C | G | 1 | a0001c0001t0002g0190 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.187+3438G>C | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 1/26 | chr5 | 55303949 | |||||||
| chr5:55304064 | A | G | 4 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 others(1): Show |
4 | NA18987.hp2 NA19001.hp1 NA19072.hp1 others(1): Show |
intron_variant | MODIFIER | c.187+3323T>C | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 1/26 | chr5 | 55304064 | |||||||
| chr5:55304259 | A | C | 1 | a0001c0002t0001g0030 | 2 | HG02630.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.187+3128T>G | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 1/26 | chr5 | 55304259 | |||||||
| chr5:55304309 | C | CT | 72 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(69): Show |
91 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(88): Show |
intron_variant | MODIFIER | c.187+3077dupA | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 1/26 | chr5 | 55304309 | |||||||
| chr5:55304309 | C | CTT | 8 | a0001c0002t0001g0037 a0001c0002t0001g0038 a0001c0002t0001g0039 others(5): Show |
8 | HG02109.hp2 HG02280.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.187+3076_187+3077d others(4): Show |
DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 1/26 | chr5 | 55304309 | |||||||
| chr5:55304309 | CT | C | 33 | a0001c0001t0001g0020 a0001c0001t0001g0139 a0001c0001t0001g0140 others(30): Show |
46 | HG00423.hp1 HG00609.hp1 HG00741.hp1 others(43): Show |
intron_variant | MODIFIER | c.187+3077delA | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 1/26 | chr5 | 55304309 | |||||||
| chr5:55304338 | G | A | 4 | a0001c0001t0001g0142 a0001c0002t0001g0037 a0001c0002t0001g0038 others(1): Show |
4 | HG02109.hp2 HG02615.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.187+3049C>T | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 1/26 | chr5 | 55304338 | |||||||
| chr5:55304482 | T | G | 1 | a0007c0010t0001g0184 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.187+2905A>C | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 1/26 | chr5 | 55304482 | |||||||
| chr5:55304498 | G | A | 1 | a0001c0002t0001g0039 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.187+2889C>T | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 1/26 | chr5 | 55304498 | |||||||
| chr5:55304626 | C | G | 2 | a0002c0004t0004g0042 a0002c0004t0004g0043 |
2 | HG01168.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.187+2761G>C | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 1/26 | chr5 | 55304626 | |||||||
| chr5:55304646 | T | C | 1 | a0001c0001t0001g0185 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.187+2741A>G | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 1/26 | chr5 | 55304646 | |||||||
| chr5:55304729 | G | A | 51 | a0001c0002t0001g0002 a0001c0002t0001g0004 a0001c0002t0001g0007 others(48): Show |
70 | HG00423.hp2 HG00621.hp2 HG00733.hp2 others(67): Show |
intron_variant | MODIFIER | c.187+2658C>T | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 1/26 | chr5 | 55304729 | |||||||
| chr5:55304846 | A | G | 51 | a0001c0002t0001g0002 a0001c0002t0001g0004 a0001c0002t0001g0007 others(48): Show |
70 | HG00423.hp2 HG00621.hp2 HG00733.hp2 others(67): Show |
intron_variant | MODIFIER | c.187+2541T>C | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 1/26 | chr5 | 55304846 | |||||||
| chr5:55305070 | A | G | 102 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(99): Show |
133 | HG00423.hp2 HG00609.hp1 HG00621.hp2 others(130): Show |
intron_variant | MODIFIER | c.187+2317T>C | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 1/26 | chr5 | 55305070 | |||||||
| chr5:55305125 | C | T | 2 | a0002c0004t0004g0042 a0002c0004t0004g0043 |
2 | HG01168.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.187+2262G>A | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 1/26 | chr5 | 55305125 | |||||||
| chr5:55305126 | T | A | 2 | a0002c0004t0004g0042 a0002c0004t0004g0043 |
2 | HG01168.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.187+2261A>T | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 1/26 | chr5 | 55305126 | |||||||
| chr5:55305177 | C | T | 1 | a0001c0001t0001g0047 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.187+2210G>A | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 1/26 | chr5 | 55305177 | |||||||
| chr5:55305320 | G | C | 1 | a0001c0001t0001g0143 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.187+2067C>G | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 1/26 | chr5 | 55305320 | |||||||
| chr5:55305420 | G | A | 1 | a0001c0001t0001g0144 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.187+1967C>T | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 1/26 | chr5 | 55305420 | |||||||
| chr5:55305444 | G | T | 1 | a0001c0001t0001g0046 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.187+1943C>A | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 1/26 | chr5 | 55305444 | |||||||
| chr5:55305624 | T | C | 50 | a0001c0001t0001g0005 a0001c0001t0001g0021 a0001c0001t0001g0022 others(47): Show |
59 | HG00140.hp1 HG00423.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.187+1763A>G | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 1/26 | chr5 | 55305624 | |||||||
| chr5:55305635 | C | G | 1 | a0001c0001t0001g0045 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.187+1752G>C | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 1/26 | chr5 | 55305635 | |||||||
| chr5:55305697 | G | A | 1 | a0001c0001t0001g0186 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.187+1690C>T | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 1/26 | chr5 | 55305697 | |||||||
| chr5:55306179 | C | T | 3 | a0001c0001t0002g0027 a0001c0001t0002g0187 a0001c0001t0002g0188 |
4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.187+1208G>A | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 1/26 | chr5 | 55306179 | |||||||
| chr5:55306427 | C | G | 2 | a0002c0004t0004g0042 a0002c0004t0004g0043 |
2 | HG01168.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.187+960G>C | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 1/26 | chr5 | 55306427 | |||||||
| chr5:55306528 | CTG | C | 29 | a0001c0001t0002g0006 a0001c0001t0002g0010 a0001c0001t0002g0011 others(26): Show |
41 | HG00609.hp1 HG00741.hp1 HG01433.hp1 others(38): Show |
intron_variant | MODIFIER | c.187+857_187+858del others(2): Show |
DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 1/26 | chr5 | 55306528 | |||||||
| chr5:55306545 | T | C | 2 | a0002c0004t0004g0042 a0002c0004t0004g0043 |
2 | HG01168.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.187+842A>G | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 1/26 | chr5 | 55306545 | |||||||
| chr5:55306655 | A | G | 1 | a0001c0001t0001g0044 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.187+732T>C | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 1/26 | chr5 | 55306655 | |||||||
| chr5:55306885 | A | G | 4 | a0001c0002t0001g0040 a0001c0002t0001g0041 a0002c0004t0004g0042 others(1): Show |
4 | HG01168.hp2 HG02486.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.187+502T>C | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 1/26 | chr5 | 55306885 | |||||||
| chr5:55307095 | A | G | 2 | a0001c0002t0001g0040 a0001c0002t0001g0041 |
2 | HG02486.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.187+292T>C | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 1/26 | chr5 | 55307095 | |||||||
| chr5:55307229 | T | A | 61 | a0001c0002t0001g0002 a0001c0002t0001g0004 a0001c0002t0001g0007 others(58): Show |
80 | HG00423.hp2 HG00621.hp2 HG00733.hp2 others(77): Show |
intron_variant | MODIFIER | c.187+158A>T | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 1/26 | chr5 | 55307229 | |||||||
| chr5:55307276 | G | A | 4 | a0001c0001t0001g0260 a0001c0001t0001g0261 a0001c0001t0001g0262 others(1): Show |
4 | NA18991.hp2 NA18997.hp2 NA19012.hp2 others(1): Show |
intron_variant | MODIFIER | c.187+111C>T | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 1/26 | chr5 | 55307276 | |||||||
| chr5:55307297 | C | T | 3 | a0001c0002t0001g0037 a0001c0002t0001g0038 a0001c0002t0001g0039 |
3 | HG02109.hp2 HG02615.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.187+90G>A | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 1/26 | chr5 | 55307297 | |||||||
| chr5:55307313 | T | C | 1 | a0001c0001t0001g0014 | 3 | NA18968.hp1 NA19011.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.187+74A>G | DHX29 | ENSG00000067248.11 | transcript | ENST00000251636.10 | protein_coding | 1/26 | chr5 | 55307313 |