Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 401494 |
| ensemblid | ENSG00000188921.14 |
| hgncid | 20920 |
| symbol | HACD4 |
| name | 3-hydroxyacyl-CoA dehydratase 4 |
| refseq_nuc | NM_001010915.5 |
| refseq_prot | NP_001010915.2 |
| ensembl_nuc | ENST00000495827.3 |
| ensembl_prot | ENSP00000419503.1 |
| mane_status | MANE Select |
| chr | chr9 |
| start | 20999509 |
| end | 21031640 |
| strand | - |
| ver | v1.2 |
| region | chr9:20999509-21031640 |
| region5000 | chr9:20994509-21036640 |
| regionname0 | HACD4_chr9_20999509_21031640 |
| regionname5000 | HACD4_chr9_20994509_21036640 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 232 | 244 | 64 | 46 | 93 | 11 | 28 | 72 | HACD4_chr9_20994509_21036640 | HACD4 | MGPLA others(227): Show |
chr9 | 20994509 | 21036640 |
| a0002 | 0/0 | 232 | 186 | 34 | 20 | 117 | 3 | 12 | 97 | HACD4_chr9_20994509_21036640 | HACD4 | MGPLA others(227): Show |
chr9 | 20994509 | 21036640 |
| a0003 | 0/0 | 232 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | MGPLA others(227): Show |
chr9 | 20994509 | 21036640 |
| a0004 | 0/0 | 232 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | MGPLA others(227): Show |
chr9 | 20994509 | 21036640 |
| a0005 | 0/0 | 232 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | MGPLA others(227): Show |
chr9 | 20994509 | 21036640 |
| a0006 | 0/0 | 232 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HACD4_chr9_20994509_21036640 | HACD4 | MGPLA others(227): Show |
chr9 | 20994509 | 21036640 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 696 | 243 | 63 | 46 | 93 | 11 | 28 | HACD4_chr9_20994509_21036640 | HACD4 | ATGGG others(691): Show |
chr9 | 20994509 | 21036640 | ||
| a0001c0005 | 0/0 | 696 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | ATGGG others(691): Show |
chr9 | 20994509 | 21036640 | ||
| a0002c0002 | 0/0 | 696 | 183 | 34 | 20 | 114 | 3 | 12 | HACD4_chr9_20994509_21036640 | HACD4 | ATGGG others(691): Show |
chr9 | 20994509 | 21036640 | ||
| a0002c0003 | 0/0 | 696 | 3 | 0 | 0 | 3 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | ATGGG others(691): Show |
chr9 | 20994509 | 21036640 | ||
| a0003c0006 | 0/0 | 696 | 1 | 0 | 1 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | ATGGG others(691): Show |
chr9 | 20994509 | 21036640 | ||
| a0004c0004 | 0/0 | 696 | 1 | 0 | 1 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | ATGGG others(691): Show |
chr9 | 20994509 | 21036640 | ||
| a0005c0007 | 0/0 | 696 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | ATGGG others(691): Show |
chr9 | 20994509 | 21036640 | ||
| a0006c0008 | 0/0 | 696 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | ATGGG others(691): Show |
chr9 | 20994509 | 21036640 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 8278 | 2 | 0 | 0 | 0 | 2 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | CCCCG others(8273): Show |
chr9 | 20994509 | 21036640 |
| a0001c0001t0002 | 0/0 | 8278 | 10 | 3 | 4 | 3 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | CCCCG others(8273): Show |
chr9 | 20994509 | 21036640 |
| a0001c0001t0003 | 0/0 | 8278 | 53 | 1 | 10 | 37 | 2 | 3 | HACD4_chr9_20994509_21036640 | HACD4 | CCCCG others(8273): Show |
chr9 | 20994509 | 21036640 |
| a0001c0001t0004 | 0/0 | 8278 | 32 | 9 | 2 | 12 | 2 | 7 | HACD4_chr9_20994509_21036640 | HACD4 | CCCCG others(8273): Show |
chr9 | 20994509 | 21036640 |
| a0001c0001t0005 | 0/0 | 8277 | 26 | 0 | 3 | 14 | 3 | 6 | HACD4_chr9_20994509_21036640 | HACD4 | CCCCG others(8272): Show |
chr9 | 20994509 | 21036640 |
| a0001c0001t0006 | 0/0 | 8277 | 23 | 5 | 10 | 0 | 0 | 8 | HACD4_chr9_20994509_21036640 | HACD4 | CCCCG others(8272): Show |
chr9 | 20994509 | 21036640 |
| a0001c0001t0007 | 0/0 | 8278 | 14 | 0 | 0 | 13 | 0 | 1 | HACD4_chr9_20994509_21036640 | HACD4 | CCCCG others(8273): Show |
chr9 | 20994509 | 21036640 |
| a0001c0001t0010 | 1/0 | 8277 | 11 | 10 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | CCCCG others(8272): Show |
chr9 | 20994509 | 21036640 |
| a0001c0001t0011 | 0/0 | 8278 | 9 | 9 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | CCCCG others(8273): Show |
chr9 | 20994509 | 21036640 |
| a0001c0001t0012 | 0/0 | 8278 | 8 | 0 | 0 | 7 | 0 | 1 | HACD4_chr9_20994509_21036640 | HACD4 | CCCCG others(8273): Show |
chr9 | 20994509 | 21036640 |
| a0001c0001t0013 | 0/0 | 8278 | 10 | 6 | 3 | 0 | 1 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | CCCCG others(8273): Show |
chr9 | 20994509 | 21036640 |
| a0001c0001t0014 | 0/0 | 8277 | 8 | 4 | 4 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | CCCCG others(8272): Show |
chr9 | 20994509 | 21036640 |
| a0001c0001t0016 | 0/0 | 8278 | 3 | 0 | 3 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | CCCCG others(8273): Show |
chr9 | 20994509 | 21036640 |
| a0001c0001t0017 | 0/0 | 8278 | 3 | 3 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | CCCCG others(8273): Show |
chr9 | 20994509 | 21036640 |
| a0001c0001t0018 | 0/0 | 8155 | 3 | 3 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | CCCCG others(8150): Show |
chr9 | 20994509 | 21036640 |
| a0001c0001t0019 | 0/0 | 8278 | 3 | 2 | 1 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | CCCCG others(8273): Show |
chr9 | 20994509 | 21036640 |
| a0001c0001t0020 | 0/0 | 8278 | 3 | 3 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | CCCCG others(8273): Show |
chr9 | 20994509 | 21036640 |
| a0001c0001t0021 | 0/0 | 8277 | 2 | 0 | 0 | 2 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | CCCCG others(8272): Show |
chr9 | 20994509 | 21036640 |
| a0001c0001t0024 | 0/0 | 8278 | 2 | 0 | 2 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | CCCCG others(8273): Show |
chr9 | 20994509 | 21036640 |
| a0001c0001t0025 | 0/0 | 8276 | 2 | 0 | 0 | 2 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | CCCCG others(8271): Show |
chr9 | 20994509 | 21036640 |
| a0001c0001t0027 | 0/0 | 8277 | 1 | 0 | 1 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | CCCCG others(8272): Show |
chr9 | 20994509 | 21036640 |
| a0001c0001t0028 | 0/0 | 8278 | 1 | 0 | 0 | 0 | 0 | 1 | HACD4_chr9_20994509_21036640 | HACD4 | CCCCG others(8273): Show |
chr9 | 20994509 | 21036640 |
| a0001c0001t0029 | 0/0 | 8277 | 1 | 0 | 1 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | CCCCG others(8272): Show |
chr9 | 20994509 | 21036640 |
| a0001c0001t0030 | 0/0 | 8277 | 1 | 0 | 1 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | CCCCG others(8272): Show |
chr9 | 20994509 | 21036640 |
| a0001c0001t0031 | 0/0 | 8277 | 1 | 0 | 0 | 0 | 1 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | CCCCG others(8272): Show |
chr9 | 20994509 | 21036640 |
| a0001c0001t0032 | 0/1 | 8277 | 1 | 0 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | CCCCG others(8272): Show |
chr9 | 20994509 | 21036640 |
| a0001c0001t0034 | 0/0 | 8278 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | CCCCG others(8273): Show |
chr9 | 20994509 | 21036640 |
| a0001c0001t0035 | 0/0 | 8278 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | CCCCG others(8273): Show |
chr9 | 20994509 | 21036640 |
| a0001c0001t0036 | 0/0 | 8278 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | CCCCG others(8273): Show |
chr9 | 20994509 | 21036640 |
| a0001c0001t0037 | 0/0 | 8278 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | CCCCG others(8273): Show |
chr9 | 20994509 | 21036640 |
| a0001c0001t0039 | 0/0 | 8278 | 1 | 0 | 0 | 0 | 0 | 1 | HACD4_chr9_20994509_21036640 | HACD4 | CCCCG others(8273): Show |
chr9 | 20994509 | 21036640 |
| a0001c0001t0045 | 0/0 | 8278 | 1 | 0 | 1 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | CCCCG others(8273): Show |
chr9 | 20994509 | 21036640 |
| a0001c0001t0051 | 0/0 | 8276 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | CCCCG others(8271): Show |
chr9 | 20994509 | 21036640 |
| a0001c0001t0052 | 0/0 | 8278 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | CCCCG others(8273): Show |
chr9 | 20994509 | 21036640 |
| a0001c0001t0053 | 0/0 | 8278 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | CCCCG others(8273): Show |
chr9 | 20994509 | 21036640 |
| a0001c0001t0055 | 0/0 | 8277 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | CCCCG others(8272): Show |
chr9 | 20994509 | 21036640 |
| a0001c0005t0010 | 0/0 | 8277 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | CCCCG others(8272): Show |
chr9 | 20994509 | 21036640 |
| a0002c0002t0001 | 0/0 | 8278 | 68 | 3 | 14 | 45 | 1 | 5 | HACD4_chr9_20994509_21036640 | HACD4 | CCCCG others(8273): Show |
chr9 | 20994509 | 21036640 |
| a0002c0002t0002 | 0/0 | 8278 | 50 | 5 | 4 | 34 | 2 | 5 | HACD4_chr9_20994509_21036640 | HACD4 | CCCCG others(8273): Show |
chr9 | 20994509 | 21036640 |
| a0002c0002t0003 | 0/0 | 8278 | 2 | 0 | 0 | 2 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | CCCCG others(8273): Show |
chr9 | 20994509 | 21036640 |
| a0002c0002t0004 | 0/0 | 8278 | 5 | 0 | 0 | 5 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | CCCCG others(8273): Show |
chr9 | 20994509 | 21036640 |
| a0002c0002t0008 | 0/0 | 8278 | 14 | 12 | 1 | 0 | 0 | 1 | HACD4_chr9_20994509_21036640 | HACD4 | CCCCG others(8273): Show |
chr9 | 20994509 | 21036640 |
| a0002c0002t0009 | 0/0 | 8277 | 14 | 0 | 0 | 14 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | CCCCG others(8272): Show |
chr9 | 20994509 | 21036640 |
| a0002c0002t0010 | 0/0 | 8277 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | CCCCG others(8272): Show |
chr9 | 20994509 | 21036640 |
| a0002c0002t0011 | 0/0 | 8278 | 3 | 3 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | CCCCG others(8273): Show |
chr9 | 20994509 | 21036640 |
| a0002c0002t0012 | 0/0 | 8278 | 2 | 0 | 0 | 2 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | CCCCG others(8273): Show |
chr9 | 20994509 | 21036640 |
| a0002c0002t0014 | 0/0 | 8277 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | CCCCG others(8272): Show |
chr9 | 20994509 | 21036640 |
| a0002c0002t0015 | 0/0 | 8278 | 5 | 5 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | CCCCG others(8273): Show |
chr9 | 20994509 | 21036640 |
| a0002c0002t0022 | 0/0 | 8278 | 2 | 0 | 0 | 2 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | CCCCG others(8273): Show |
chr9 | 20994509 | 21036640 |
| a0002c0002t0023 | 0/0 | 8278 | 2 | 0 | 0 | 2 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | CCCCG others(8273): Show |
chr9 | 20994509 | 21036640 |
| a0002c0002t0026 | 0/0 | 8278 | 2 | 2 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | CCCCG others(8273): Show |
chr9 | 20994509 | 21036640 |
| a0002c0002t0033 | 0/0 | 8278 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | CCCCG others(8273): Show |
chr9 | 20994509 | 21036640 |
| a0002c0002t0038 | 0/0 | 8278 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | CCCCG others(8273): Show |
chr9 | 20994509 | 21036640 |
| a0002c0002t0041 | 0/0 | 8278 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | CCCCG others(8273): Show |
chr9 | 20994509 | 21036640 |
| a0002c0002t0042 | 0/0 | 8278 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | CCCCG others(8273): Show |
chr9 | 20994509 | 21036640 |
| a0002c0002t0043 | 0/0 | 8278 | 1 | 0 | 1 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | CCCCG others(8273): Show |
chr9 | 20994509 | 21036640 |
| a0002c0002t0044 | 0/0 | 8278 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | CCCCG others(8273): Show |
chr9 | 20994509 | 21036640 |
| a0002c0002t0046 | 0/0 | 8278 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | CCCCG others(8273): Show |
chr9 | 20994509 | 21036640 |
| a0002c0002t0047 | 0/0 | 8278 | 1 | 0 | 0 | 0 | 0 | 1 | HACD4_chr9_20994509_21036640 | HACD4 | CCCCG others(8273): Show |
chr9 | 20994509 | 21036640 |
| a0002c0002t0048 | 0/0 | 8278 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | CCCCG others(8273): Show |
chr9 | 20994509 | 21036640 |
| a0002c0002t0049 | 0/0 | 8278 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | CCCCG others(8273): Show |
chr9 | 20994509 | 21036640 |
| a0002c0002t0050 | 0/0 | 8278 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | CCCCG others(8273): Show |
chr9 | 20994509 | 21036640 |
| a0002c0002t0054 | 0/0 | 8278 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | CCCCG others(8273): Show |
chr9 | 20994509 | 21036640 |
| a0002c0003t0001 | 0/0 | 8278 | 2 | 0 | 0 | 2 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | CCCCG others(8273): Show |
chr9 | 20994509 | 21036640 |
| a0002c0003t0040 | 0/0 | 8278 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | CCCCG others(8273): Show |
chr9 | 20994509 | 21036640 |
| a0003c0006t0003 | 0/0 | 8278 | 1 | 0 | 1 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | CCCCG others(8273): Show |
chr9 | 20994509 | 21036640 |
| a0004c0004t0003 | 0/0 | 8278 | 1 | 0 | 1 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | CCCCG others(8273): Show |
chr9 | 20994509 | 21036640 |
| a0005c0007t0001 | 0/0 | 8278 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | CCCCG others(8273): Show |
chr9 | 20994509 | 21036640 |
| a0006c0008t0002 | 0/0 | 8278 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | CCCCG others(8273): Show |
chr9 | 20994509 | 21036640 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0002g0037 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0002g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0002g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0003g0002 | 0/0 | 18 | 0 | 2 | 14 | 1 | 1 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0003g0013 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0003g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0003g0016 | 0/0 | 4 | 0 | 1 | 0 | 1 | 2 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0003g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0003g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0003g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0003g0046 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0003g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0003g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0003g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0003g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0003g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0003g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0003g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0003g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0003g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0003g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0003g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0004g0009 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0004g0012 | 0/0 | 5 | 0 | 0 | 1 | 0 | 4 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0004g0019 | 0/0 | 4 | 0 | 2 | 0 | 2 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0004g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0004g0038 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0004g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0004g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0004g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0004g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0004g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0004g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0004g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0004g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0004g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0004g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0004g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0004g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0005g0005 | 0/0 | 10 | 0 | 1 | 7 | 0 | 2 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0005g0011 | 0/0 | 5 | 0 | 1 | 1 | 1 | 2 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0005g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0005g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0005g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0005g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0005g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0005g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0005g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0005g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0005g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0005g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0006g0007 | 0/0 | 9 | 0 | 4 | 0 | 0 | 5 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0006g0020 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0006g0028 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0006g0029 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0006g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0006g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0006g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0006g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0006g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0006g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0006g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0007g0004 | 0/0 | 11 | 0 | 0 | 10 | 0 | 1 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0007g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0007g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0007g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0010g0010 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0010g0015 | 1/0 | 4 | 3 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0011g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0011g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0011g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0011g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0011g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0011g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0011g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0012g0023 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0012g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0012g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0012g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0012g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0012g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0013g0039 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0013g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0013g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0013g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0013g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0013g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0013g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0014g0008 | 0/0 | 7 | 4 | 3 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0014g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0016g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0016g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0016g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0017g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0017g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0017g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0018g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0018g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0019g0022 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0020g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0020g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0021g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0021g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0024g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0025g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0027g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0028g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0029g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0030g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0031g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0032g0063 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0034g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0035g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0036g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0037g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0039g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0045g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0051g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0052g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0053g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0001t0055g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0001c0005t0010g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0001g0001 | 0/0 | 26 | 2 | 6 | 17 | 0 | 1 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0001g0017 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0001g0018 | 0/0 | 4 | 1 | 3 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0001g0044 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0001g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0001g0053 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0001g0057 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0002g0003 | 0/0 | 15 | 1 | 0 | 11 | 0 | 3 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0002g0025 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0002g0026 | 0/0 | 3 | 1 | 1 | 0 | 0 | 1 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0002g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0002g0052 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0002g0058 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0002g0059 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0002g0060 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0002g0061 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0002g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0002g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0002g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0002g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0002g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0002g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0003g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0004g0024 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0004g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0004g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0008g0051 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0008g0054 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0008g0055 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0008g0056 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0008g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0008g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0008g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0008g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0008g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0008g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0009g0006 | 0/0 | 10 | 0 | 0 | 10 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0009g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0009g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0009g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0009g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0010g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0011g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0011g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0011g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0012g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0014g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0015g0050 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0015g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0015g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0015g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0022g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0022g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0023g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0023g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0026g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0026g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0033g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0038g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0041g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0042g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0043g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0044g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0046g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0047g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0048g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0049g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0050g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0002t0054g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0003t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0003t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0002c0003t0040g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0003c0006t0003g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0004c0004t0003g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0005c0007t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| a0006c0008t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0004 | g0019 | EUR | GBR | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0074 | EUR | GBR | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG00140 | hp1 | a0001 | c0001 | t0004 | g0019 | EUR | GBR | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG00140 | hp2 | a0001 | c0001 | t0005 | g0066 | EUR | GBR | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG00280 | hp1 | a0001 | c0001 | t0031 | g0078 | EUR | FIN | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG00280 | hp2 | a0002 | c0002 | t0002 | g0179 | EUR | FIN | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG00408 | hp1 | a0002 | c0003 | t0040 | g0142 | EAS | CHS | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG00408 | hp2 | a0001 | c0001 | t0034 | g0127 | EAS | CHS | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG00438 | hp1 | a0001 | c0001 | t0007 | g0128 | EAS | CHS | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG00438 | hp2 | a0002 | c0002 | t0001 | g0111 | EAS | CHS | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0037 | EAS | CHS | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG00544 | hp2 | a0002 | c0002 | t0012 | g0049 | EAS | CHS | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG00558 | hp1 | a0001 | c0001 | t0004 | g0009 | EAS | CHS | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG00558 | hp2 | a0002 | c0002 | t0001 | g0017 | EAS | CHS | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG00621 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | CHS | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG00621 | hp2 | a0001 | c0001 | t0005 | g0027 | EAS | CHS | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG00639 | hp1 | a0001 | c0001 | t0014 | g0008 | AMR | PUR | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG00639 | hp2 | a0001 | c0001 | t0004 | g0019 | AMR | PUR | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG00642 | hp1 | a0001 | c0001 | t0014 | g0110 | AMR | PUR | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG00642 | hp2 | a0001 | c0001 | t0003 | g0235 | AMR | PUR | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG00673 | hp1 | a0001 | c0001 | t0003 | g0120 | EAS | CHS | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG00673 | hp2 | a0002 | c0002 | t0004 | g0024 | EAS | CHS | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG00733 | hp1 | a0001 | c0001 | t0006 | g0020 | AMR | PUR | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG00733 | hp2 | a0003 | c0006 | t0003 | g0157 | AMR | PUR | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG00735 | hp1 | a0001 | c0001 | t0013 | g0136 | AMR | PUR | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG00735 | hp2 | a0002 | c0002 | t0002 | g0187 | AMR | PUR | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG00738 | hp1 | a0002 | c0002 | t0002 | g0025 | AMR | PUR | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG00738 | hp2 | a0001 | c0001 | t0005 | g0011 | AMR | PUR | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG00741 | hp1 | a0001 | c0001 | t0004 | g0019 | AMR | PUR | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG00741 | hp2 | a0001 | c0001 | t0006 | g0029 | AMR | PUR | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG01069 | hp1 | a0001 | c0001 | t0014 | g0008 | AMR | PUR | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG01069 | hp2 | a0002 | c0002 | t0002 | g0213 | AMR | PUR | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG01070 | hp1 | a0001 | c0001 | t0024 | g0036 | AMR | PUR | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG01070 | hp2 | a0001 | c0001 | t0006 | g0112 | AMR | PUR | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG01071 | hp1 | a0001 | c0001 | t0014 | g0008 | AMR | PUR | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG01071 | hp2 | a0001 | c0001 | t0024 | g0036 | AMR | PUR | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG01074 | hp1 | a0001 | c0001 | t0003 | g0141 | AMR | PUR | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG01074 | hp2 | a0001 | c0001 | t0019 | g0022 | AMR | PUR | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG01081 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | PUR | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG01081 | hp2 | a0001 | c0001 | t0013 | g0039 | AMR | PUR | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG01099 | hp1 | a0001 | c0001 | t0030 | g0135 | AMR | PUR | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG01099 | hp2 | a0001 | c0001 | t0003 | g0016 | AMR | PUR | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG01106 | hp1 | a0002 | c0002 | t0001 | g0217 | AMR | PUR | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG01106 | hp2 | a0001 | c0001 | t0006 | g0113 | AMR | PUR | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG01109 | hp1 | a0002 | c0002 | t0001 | g0243 | AMR | PUR | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG01109 | hp2 | a0001 | c0001 | t0003 | g0116 | AMR | PUR | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG01167 | hp1 | a0001 | c0001 | t0016 | g0065 | AMR | PUR | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG01167 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG01243 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0109 | AMR | PUR | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG01255 | hp1 | a0004 | c0004 | t0003 | g0118 | AMR | CLM | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG01255 | hp2 | a0001 | c0001 | t0013 | g0138 | AMR | CLM | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG01256 | hp1 | a0001 | c0001 | t0006 | g0007 | AMR | CLM | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG01256 | hp2 | a0002 | c0002 | t0002 | g0026 | AMR | CLM | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG01257 | hp1 | a0001 | c0001 | t0003 | g0114 | AMR | CLM | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG01257 | hp2 | a0001 | c0001 | t0006 | g0007 | AMR | CLM | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG01258 | hp1 | a0001 | c0001 | t0003 | g0115 | AMR | CLM | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG01258 | hp2 | a0001 | c0001 | t0006 | g0020 | AMR | CLM | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG01261 | hp1 | a0002 | c0002 | t0001 | g0195 | AMR | CLM | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG01261 | hp2 | a0002 | c0002 | t0008 | g0231 | AMR | CLM | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0140 | AMR | CLM | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG01346 | hp2 | a0002 | c0002 | t0043 | g0226 | AMR | CLM | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG01358 | hp1 | a0001 | c0001 | t0045 | g0069 | AMR | CLM | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG01358 | hp2 | a0001 | c0001 | t0003 | g0046 | AMR | CLM | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG01361 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | CLM | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG01361 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | CLM | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG01433 | hp1 | a0001 | c0001 | t0027 | g0067 | AMR | CLM | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG01433 | hp2 | a0001 | c0001 | t0016 | g0077 | AMR | CLM | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG01515 | hp1 | a0001 | c0001 | t0003 | g0016 | EUR | IBS | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG01515 | hp2 | a0001 | c0001 | t0005 | g0011 | EUR | IBS | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG01516 | hp1 | a0001 | c0001 | t0013 | g0134 | EUR | IBS | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG01516 | hp2 | a0001 | c0001 | t0005 | g0081 | EUR | IBS | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG01884 | hp1 | a0002 | c0002 | t0011 | g0166 | AFR | ACB | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG01884 | hp2 | a0002 | c0002 | t0038 | g0216 | AFR | ACB | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG01891 | hp1 | a0001 | c0001 | t0011 | g0032 | AFR | ACB | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG01891 | hp2 | a0001 | c0001 | t0010 | g0010 | AFR | ACB | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG01928 | hp1 | a0001 | c0001 | t0029 | g0121 | AMR | PEL | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG01928 | hp2 | a0002 | c0002 | t0001 | g0018 | AMR | PEL | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG01934 | hp1 | a0001 | c0001 | t0005 | g0064 | AMR | PEL | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG01934 | hp2 | a0001 | c0001 | t0003 | g0046 | AMR | PEL | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG01975 | hp1 | a0002 | c0002 | t0001 | g0209 | AMR | PEL | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG01975 | hp2 | a0002 | c0002 | t0001 | g0242 | AMR | PEL | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG01981 | hp1 | a0001 | c0001 | t0006 | g0007 | AMR | PEL | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG01981 | hp2 | a0002 | c0002 | t0001 | g0018 | AMR | PEL | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0037 | AMR | PEL | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG01993 | hp2 | a0002 | c0002 | t0001 | g0018 | AMR | PEL | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02004 | hp1 | a0001 | c0001 | t0006 | g0007 | AMR | PEL | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02004 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PEL | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02027 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | KHV | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02027 | hp2 | a0001 | c0001 | t0003 | g0035 | EAS | KHV | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02040 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | KHV | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02040 | hp2 | a0001 | c0001 | t0003 | g0014 | EAS | KHV | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02055 | hp1 | a0001 | c0001 | t0013 | g0040 | AFR | ACB | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02055 | hp2 | a0002 | c0002 | t0008 | g0238 | AFR | ACB | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02056 | hp1 | a0001 | c0001 | t0004 | g0009 | EAS | KHV | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02056 | hp2 | a0001 | c0001 | t0004 | g0012 | EAS | KHV | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02071 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | KHV | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02071 | hp2 | a0001 | c0001 | t0025 | g0042 | EAS | KHV | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02074 | hp1 | a0001 | c0001 | t0004 | g0009 | EAS | KHV | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02074 | hp2 | a0002 | c0002 | t0001 | g0048 | EAS | KHV | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02080 | hp1 | a0002 | c0002 | t0054 | g0201 | EAS | KHV | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02080 | hp2 | a0001 | c0001 | t0003 | g0014 | EAS | KHV | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02083 | hp1 | a0001 | c0001 | t0003 | g0014 | EAS | KHV | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02083 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | KHV | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02129 | hp1 | a0002 | c0002 | t0001 | g0057 | EAS | KHV | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02129 | hp2 | a0002 | c0002 | t0002 | g0220 | EAS | KHV | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02132 | hp1 | a0002 | c0002 | t0002 | g0060 | EAS | KHV | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02132 | hp2 | a0001 | c0001 | t0004 | g0126 | EAS | KHV | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0123 | EAS | KHV | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02135 | hp2 | a0002 | c0002 | t0022 | g0233 | EAS | KHV | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02145 | hp1 | a0001 | c0001 | t0006 | g0020 | AFR | ACB | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02145 | hp2 | a0002 | c0002 | t0002 | g0026 | AFR | ACB | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02148 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PEL | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02148 | hp2 | a0001 | c0001 | t0006 | g0076 | AMR | PEL | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02155 | hp1 | a0002 | c0002 | t0001 | g0057 | EAS | CDX | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02155 | hp2 | a0002 | c0002 | t0003 | g0185 | EAS | CDX | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02165 | hp1 | a0001 | c0001 | t0003 | g0014 | EAS | CDX | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02165 | hp2 | a0001 | c0001 | t0004 | g0009 | EAS | CDX | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02257 | hp1 | a0001 | c0001 | t0010 | g0010 | AFR | ACB | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02257 | hp2 | a0001 | c0001 | t0036 | g0088 | AFR | ACB | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02258 | hp1 | a0002 | c0002 | t0008 | g0051 | AFR | ACB | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02258 | hp2 | a0001 | c0001 | t0053 | g0148 | AFR | ACB | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02280 | hp1 | a0001 | c0001 | t0013 | g0137 | AFR | ACB | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02280 | hp2 | a0001 | c0005 | t0010 | g0092 | AFR | ACB | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02300 | hp1 | a0001 | c0001 | t0016 | g0080 | AMR | PEL | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02300 | hp2 | a0001 | c0001 | t0005 | g0005 | AMR | PEL | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02451 | hp1 | a0001 | c0001 | t0055 | g0161 | AFR | ACB | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02451 | hp2 | a0001 | c0001 | t0019 | g0022 | AFR | ACB | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02523 | hp1 | a0002 | c0002 | t0002 | g0143 | EAS | KHV | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02523 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | KHV | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02572 | hp1 | a0001 | c0001 | t0011 | g0087 | AFR | GWD | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02572 | hp2 | a0001 | c0001 | t0018 | g0034 | AFR | GWD | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02602 | hp1 | a0002 | c0002 | t0047 | g0204 | SAS | PJL | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02602 | hp2 | a0001 | c0001 | t0028 | g0082 | SAS | PJL | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02615 | hp1 | a0002 | c0002 | t0026 | g0228 | AFR | GWD | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02615 | hp2 | a0002 | c0002 | t0002 | g0058 | AFR | GWD | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0108 | AFR | GWD | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02622 | hp2 | a0002 | c0002 | t0010 | g0207 | AFR | GWD | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02630 | hp1 | a0002 | c0002 | t0008 | g0055 | AFR | GWD | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02630 | hp2 | a0001 | c0001 | t0004 | g0098 | AFR | GWD | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02647 | hp1 | a0001 | c0001 | t0004 | g0033 | AFR | GWD | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02647 | hp2 | a0001 | c0001 | t0014 | g0008 | AFR | GWD | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02683 | hp1 | a0001 | c0001 | t0005 | g0005 | SAS | PJL | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02683 | hp2 | a0001 | c0001 | t0039 | g0122 | SAS | PJL | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02698 | hp1 | a0001 | c0001 | t0003 | g0016 | SAS | PJL | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02698 | hp2 | a0001 | c0001 | t0006 | g0029 | SAS | PJL | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02717 | hp1 | a0001 | c0001 | t0017 | g0100 | AFR | GWD | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02717 | hp2 | a0001 | c0001 | t0010 | g0010 | AFR | GWD | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02723 | hp1 | a0002 | c0002 | t0008 | g0055 | AFR | GWD | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02723 | hp2 | a0001 | c0001 | t0006 | g0147 | AFR | GWD | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02735 | hp1 | a0001 | c0001 | t0003 | g0016 | SAS | PJL | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02735 | hp2 | a0001 | c0001 | t0006 | g0007 | SAS | PJL | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02738 | hp1 | a0001 | c0001 | t0005 | g0011 | SAS | PJL | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02738 | hp2 | a0002 | c0002 | t0001 | g0001 | SAS | PJL | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02809 | hp1 | a0002 | c0002 | t0015 | g0150 | AFR | GWD | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0097 | AFR | GWD | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02818 | hp1 | a0001 | c0001 | t0013 | g0040 | AFR | GWD | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02818 | hp2 | a0001 | c0001 | t0010 | g0015 | AFR | GWD | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02895 | hp1 | a0002 | c0002 | t0008 | g0054 | AFR | GWD | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02895 | hp2 | a0001 | c0001 | t0010 | g0015 | AFR | GWD | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02896 | hp1 | a0001 | c0001 | t0037 | g0099 | AFR | GWD | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02896 | hp2 | a0002 | c0002 | t0015 | g0050 | AFR | GWD | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02897 | hp1 | a0002 | c0002 | t0015 | g0050 | AFR | GWD | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02897 | hp2 | a0001 | c0001 | t0010 | g0015 | AFR | GWD | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02922 | hp1 | a0001 | c0001 | t0011 | g0091 | AFR | ESN | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02922 | hp2 | a0002 | c0002 | t0002 | g0224 | AFR | ESN | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02965 | hp1 | a0002 | c0002 | t0008 | g0051 | AFR | ESN | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02965 | hp2 | a0001 | c0001 | t0011 | g0031 | AFR | ESN | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02970 | hp1 | a0001 | c0001 | t0018 | g0034 | AFR | ESN | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02970 | hp2 | a0001 | c0001 | t0010 | g0010 | AFR | ESN | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02976 | hp1 | a0001 | c0001 | t0004 | g0033 | AFR | ESN | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02976 | hp2 | a0002 | c0002 | t0002 | g0058 | AFR | ESN | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG03017 | hp1 | a0001 | c0001 | t0005 | g0011 | SAS | PJL | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG03017 | hp2 | a0002 | c0002 | t0001 | g0181 | SAS | PJL | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG03041 | hp1 | a0001 | c0001 | t0006 | g0146 | AFR | GWD | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG03041 | hp2 | a0002 | c0002 | t0008 | g0184 | AFR | GWD | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG03098 | hp1 | a0001 | c0001 | t0004 | g0106 | AFR | MSL | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG03098 | hp2 | a0001 | c0001 | t0014 | g0008 | AFR | MSL | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG03130 | hp1 | a0002 | c0002 | t0008 | g0056 | AFR | ESN | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG03130 | hp2 | a0002 | c0002 | t0015 | g0096 | AFR | ESN | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG03139 | hp1 | a0001 | c0001 | t0011 | g0090 | AFR | ESN | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG03139 | hp2 | a0001 | c0001 | t0004 | g0149 | AFR | ESN | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG03195 | hp1 | a0001 | c0001 | t0020 | g0085 | AFR | ESN | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG03195 | hp2 | a0002 | c0002 | t0011 | g0244 | AFR | ESN | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG03209 | hp1 | a0001 | c0001 | t0006 | g0159 | AFR | MSL | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG03209 | hp2 | a0002 | c0002 | t0050 | g0245 | AFR | MSL | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG03225 | hp1 | a0001 | c0001 | t0020 | g0030 | AFR | MSL | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG03225 | hp2 | a0002 | c0002 | t0008 | g0054 | AFR | MSL | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG03239 | hp1 | a0001 | c0001 | t0003 | g0002 | SAS | PJL | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG03239 | hp2 | a0002 | c0002 | t0002 | g0026 | SAS | PJL | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG03453 | hp1 | a0001 | c0001 | t0004 | g0086 | AFR | MSL | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG03453 | hp2 | a0001 | c0001 | t0018 | g0104 | AFR | MSL | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG03486 | hp1 | a0001 | c0001 | t0019 | g0022 | AFR | MSL | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG03486 | hp2 | a0001 | c0001 | t0013 | g0041 | AFR | MSL | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG03490 | hp1 | a0001 | c0001 | t0006 | g0028 | SAS | PJL | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG03490 | hp2 | a0001 | c0001 | t0004 | g0012 | SAS | PJL | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG03491 | hp1 | a0001 | c0001 | t0004 | g0012 | SAS | PJL | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG03491 | hp2 | a0002 | c0002 | t0002 | g0208 | SAS | PJL | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG03492 | hp1 | a0001 | c0001 | t0004 | g0012 | SAS | PJL | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG03492 | hp2 | a0001 | c0001 | t0006 | g0028 | SAS | PJL | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0158 | AFR | ESN | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG03516 | hp2 | a0001 | c0001 | t0004 | g0102 | AFR | ESN | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG03540 | hp1 | a0001 | c0001 | t0013 | g0039 | AFR | GWD | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG03540 | hp2 | a0001 | c0001 | t0006 | g0160 | AFR | GWD | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG03579 | hp1 | a0002 | c0002 | t0008 | g0186 | AFR | MSL | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG03579 | hp2 | a0002 | c0002 | t0026 | g0176 | AFR | MSL | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG03669 | hp1 | a0001 | c0001 | t0006 | g0007 | SAS | PJL | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG03669 | hp2 | a0001 | c0001 | t0012 | g0023 | SAS | PJL | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG03688 | hp1 | a0001 | c0001 | t0005 | g0079 | SAS | STU | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG03688 | hp2 | a0002 | c0002 | t0002 | g0003 | SAS | STU | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG03704 | hp1 | a0002 | c0002 | t0001 | g0230 | SAS | PJL | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG03704 | hp2 | a0002 | c0002 | t0001 | g0044 | SAS | PJL | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG03710 | hp1 | a0001 | c0001 | t0005 | g0005 | SAS | PJL | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG03710 | hp2 | a0002 | c0002 | t0002 | g0003 | SAS | PJL | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG03831 | hp1 | a0001 | c0001 | t0007 | g0004 | SAS | BEB | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG03831 | hp2 | a0001 | c0001 | t0004 | g0038 | SAS | BEB | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG03942 | hp1 | a0001 | c0001 | t0005 | g0084 | SAS | BEB | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG03942 | hp2 | a0002 | c0002 | t0001 | g0180 | SAS | BEB | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG04115 | hp1 | a0001 | c0001 | t0006 | g0007 | SAS | STU | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG04115 | hp2 | a0001 | c0001 | t0004 | g0012 | SAS | STU | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG04184 | hp1 | a0001 | c0001 | t0004 | g0131 | SAS | BEB | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG04184 | hp2 | a0002 | c0002 | t0002 | g0003 | SAS | BEB | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG04199 | hp1 | a0001 | c0001 | t0006 | g0007 | SAS | STU | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG04199 | hp2 | a0002 | c0002 | t0008 | g0205 | SAS | STU | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG04204 | hp1 | a0001 | c0001 | t0004 | g0038 | SAS | STU | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG04204 | hp2 | a0001 | c0001 | t0006 | g0007 | SAS | STU | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18522 | hp1 | a0002 | c0002 | t0008 | g0056 | AFR | YRI | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18522 | hp2 | a0001 | c0001 | t0011 | g0031 | AFR | YRI | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18612 | hp1 | a0005 | c0007 | t0001 | g0223 | EAS | CHB | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18612 | hp2 | a0001 | c0001 | t0005 | g0005 | EAS | CHB | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18747 | hp1 | a0002 | c0002 | t0033 | g0202 | EAS | CHB | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18747 | hp2 | a0001 | c0001 | t0004 | g0133 | EAS | CHB | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18906 | hp1 | a0001 | c0001 | t0017 | g0101 | AFR | YRI | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18906 | hp2 | a0001 | c0001 | t0004 | g0103 | AFR | YRI | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18939 | hp1 | a0001 | c0001 | t0003 | g0124 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18939 | hp2 | a0002 | c0002 | t0001 | g0017 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18940 | hp1 | a0002 | c0002 | t0001 | g0236 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18940 | hp2 | a0002 | c0002 | t0002 | g0192 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18941 | hp1 | a0001 | c0001 | t0007 | g0004 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18941 | hp2 | a0002 | c0002 | t0004 | g0239 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18942 | hp1 | a0002 | c0002 | t0022 | g0234 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18942 | hp2 | a0001 | c0001 | t0007 | g0004 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18943 | hp1 | a0001 | c0001 | t0005 | g0027 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18943 | hp2 | a0001 | c0001 | t0051 | g0139 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18944 | hp1 | a0002 | c0002 | t0002 | g0025 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18944 | hp2 | a0002 | c0002 | t0009 | g0006 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18945 | hp1 | a0002 | c0002 | t0009 | g0006 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18945 | hp2 | a0001 | c0001 | t0012 | g0023 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18946 | hp1 | a0001 | c0001 | t0005 | g0070 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18946 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18948 | hp1 | a0002 | c0002 | t0001 | g0221 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18948 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18949 | hp1 | a0002 | c0002 | t0002 | g0163 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18949 | hp2 | a0002 | c0002 | t0001 | g0017 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18950 | hp1 | a0001 | c0001 | t0007 | g0004 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18950 | hp2 | a0002 | c0002 | t0001 | g0218 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18951 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18951 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18952 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18952 | hp2 | a0002 | c0002 | t0002 | g0145 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18953 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18953 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18954 | hp1 | a0002 | c0002 | t0004 | g0024 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18954 | hp2 | a0001 | c0001 | t0005 | g0071 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18956 | hp1 | a0002 | c0002 | t0002 | g0144 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18956 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18957 | hp1 | a0001 | c0001 | t0005 | g0083 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18957 | hp2 | a0001 | c0001 | t0003 | g0021 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18959 | hp1 | a0002 | c0002 | t0001 | g0232 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18959 | hp2 | a0001 | c0001 | t0003 | g0021 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18960 | hp1 | a0002 | c0003 | t0001 | g0173 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18960 | hp2 | a0001 | c0001 | t0012 | g0023 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18961 | hp1 | a0001 | c0001 | t0007 | g0004 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18961 | hp2 | a0002 | c0002 | t0001 | g0017 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18963 | hp1 | a0002 | c0002 | t0042 | g0198 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18963 | hp2 | a0002 | c0002 | t0009 | g0169 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18964 | hp1 | a0002 | c0003 | t0001 | g0172 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18964 | hp2 | a0001 | c0001 | t0003 | g0013 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18965 | hp1 | a0002 | c0002 | t0001 | g0177 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18965 | hp2 | a0001 | c0001 | t0005 | g0005 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18966 | hp1 | a0002 | c0002 | t0001 | g0219 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18966 | hp2 | a0001 | c0001 | t0005 | g0011 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18967 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18967 | hp2 | a0001 | c0001 | t0025 | g0042 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18968 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18968 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18969 | hp1 | a0001 | c0001 | t0035 | g0151 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18969 | hp2 | a0002 | c0002 | t0002 | g0052 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18970 | hp1 | a0001 | c0001 | t0007 | g0004 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18970 | hp2 | a0002 | c0002 | t0002 | g0060 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18972 | hp1 | a0002 | c0002 | t0001 | g0237 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18972 | hp2 | a0006 | c0008 | t0002 | g0162 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18973 | hp1 | a0001 | c0001 | t0003 | g0013 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18973 | hp2 | a0002 | c0002 | t0023 | g0240 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18974 | hp1 | a0001 | c0001 | t0021 | g0073 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18974 | hp2 | a0002 | c0002 | t0023 | g0227 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18975 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18975 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18977 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18977 | hp2 | a0002 | c0002 | t0009 | g0170 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18978 | hp1 | a0002 | c0002 | t0001 | g0048 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18978 | hp2 | a0001 | c0001 | t0003 | g0043 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18979 | hp1 | a0001 | c0001 | t0003 | g0013 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18979 | hp2 | a0002 | c0002 | t0009 | g0171 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18980 | hp1 | a0002 | c0002 | t0041 | g0189 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18980 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18981 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18981 | hp2 | a0001 | c0001 | t0005 | g0068 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18983 | hp1 | a0002 | c0002 | t0002 | g0212 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18983 | hp2 | a0001 | c0001 | t0004 | g0009 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18984 | hp1 | a0001 | c0001 | t0003 | g0035 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18984 | hp2 | a0002 | c0002 | t0001 | g0168 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18985 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18985 | hp2 | a0002 | c0002 | t0002 | g0197 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18986 | hp1 | a0001 | c0001 | t0003 | g0043 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18986 | hp2 | a0001 | c0001 | t0012 | g0156 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18987 | hp1 | a0001 | c0001 | t0004 | g0132 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18987 | hp2 | a0002 | c0002 | t0001 | g0165 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18989 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18989 | hp2 | a0002 | c0002 | t0009 | g0006 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18990 | hp1 | a0002 | c0002 | t0002 | g0059 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18990 | hp2 | a0001 | c0001 | t0007 | g0004 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18991 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18991 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18992 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18992 | hp2 | a0002 | c0002 | t0004 | g0182 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18993 | hp1 | a0001 | c0001 | t0003 | g0013 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18993 | hp2 | a0002 | c0002 | t0009 | g0006 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18994 | hp1 | a0002 | c0002 | t0002 | g0025 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18994 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18995 | hp1 | a0001 | c0001 | t0005 | g0005 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18995 | hp2 | a0002 | c0002 | t0001 | g0225 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18997 | hp1 | a0002 | c0002 | t0012 | g0049 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18997 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18998 | hp1 | a0002 | c0002 | t0002 | g0229 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18998 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18999 | hp1 | a0002 | c0002 | t0009 | g0006 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18999 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA19000 | hp1 | a0001 | c0001 | t0007 | g0004 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA19000 | hp2 | a0001 | c0001 | t0003 | g0021 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA19001 | hp1 | a0002 | c0002 | t0001 | g0190 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA19001 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA19002 | hp1 | a0002 | c0002 | t0009 | g0006 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA19002 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA19003 | hp1 | a0002 | c0002 | t0009 | g0006 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0117 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA19004 | hp1 | a0001 | c0001 | t0003 | g0047 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA19004 | hp2 | a0001 | c0001 | t0007 | g0130 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA19006 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA19006 | hp2 | a0002 | c0002 | t0001 | g0214 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA19009 | hp1 | a0002 | c0002 | t0002 | g0061 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA19009 | hp2 | a0001 | c0001 | t0005 | g0005 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA19030 | hp1 | a0001 | c0001 | t0014 | g0008 | AFR | LWK | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA19030 | hp2 | a0001 | c0001 | t0004 | g0093 | AFR | LWK | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA19043 | hp1 | a0002 | c0002 | t0014 | g0206 | AFR | LWK | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA19043 | hp2 | a0001 | c0001 | t0011 | g0094 | AFR | LWK | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA19054 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA19054 | hp2 | a0001 | c0001 | t0021 | g0072 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA19056 | hp1 | a0002 | c0002 | t0001 | g0053 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA19056 | hp2 | a0002 | c0002 | t0001 | g0222 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA19058 | hp1 | a0002 | c0002 | t0001 | g0194 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA19058 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA19060 | hp1 | a0002 | c0002 | t0004 | g0024 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA19060 | hp2 | a0002 | c0002 | t0002 | g0045 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA19062 | hp1 | a0002 | c0002 | t0003 | g0188 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA19062 | hp2 | a0001 | c0001 | t0012 | g0152 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA19064 | hp1 | a0001 | c0001 | t0005 | g0005 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA19064 | hp2 | a0001 | c0001 | t0007 | g0004 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA19065 | hp1 | a0002 | c0002 | t0002 | g0061 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA19065 | hp2 | a0001 | c0001 | t0005 | g0005 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA19066 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA19066 | hp2 | a0002 | c0002 | t0009 | g0006 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA19067 | hp1 | a0002 | c0002 | t0002 | g0211 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA19067 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA19070 | hp1 | a0002 | c0002 | t0002 | g0059 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA19070 | hp2 | a0002 | c0002 | t0001 | g0053 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA19072 | hp1 | a0001 | c0001 | t0007 | g0125 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA19072 | hp2 | a0002 | c0002 | t0044 | g0199 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA19074 | hp1 | a0002 | c0002 | t0048 | g0200 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA19074 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA19075 | hp1 | a0002 | c0002 | t0001 | g0210 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA19075 | hp2 | a0001 | c0001 | t0004 | g0009 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA19076 | hp1 | a0001 | c0001 | t0003 | g0175 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA19076 | hp2 | a0002 | c0002 | t0009 | g0164 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA19078 | hp1 | a0001 | c0001 | t0004 | g0009 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA19078 | hp2 | a0002 | c0002 | t0046 | g0196 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA19080 | hp1 | a0002 | c0002 | t0002 | g0045 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA19080 | hp2 | a0001 | c0001 | t0005 | g0005 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA19081 | hp1 | a0001 | c0001 | t0012 | g0153 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA19081 | hp2 | a0001 | c0001 | t0003 | g0174 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA19082 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA19082 | hp2 | a0002 | c0002 | t0002 | g0052 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA19083 | hp1 | a0001 | c0001 | t0004 | g0129 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA19083 | hp2 | a0001 | c0001 | t0003 | g0047 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA19084 | hp1 | a0002 | c0002 | t0049 | g0193 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA19084 | hp2 | a0002 | c0002 | t0009 | g0006 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA19085 | hp1 | a0002 | c0002 | t0002 | g0203 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA19085 | hp2 | a0001 | c0001 | t0003 | g0013 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA19088 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA19088 | hp2 | a0001 | c0001 | t0003 | g0119 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA19089 | hp1 | a0002 | c0002 | t0001 | g0183 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA19089 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA19090 | hp1 | a0001 | c0001 | t0007 | g0004 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA19090 | hp2 | a0001 | c0001 | t0012 | g0155 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA19091 | hp1 | a0002 | c0002 | t0001 | g0241 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA19091 | hp2 | a0001 | c0001 | t0012 | g0154 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA19240 | hp1 | a0001 | c0001 | t0010 | g0010 | AFR | YRI | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA19240 | hp2 | a0002 | c0002 | t0015 | g0191 | AFR | YRI | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA20129 | hp1 | a0001 | c0001 | t0052 | g0105 | AFR | ASW | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA20129 | hp2 | a0001 | c0001 | t0013 | g0041 | AFR | ASW | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA20752 | hp1 | a0002 | c0002 | t0001 | g0044 | EUR | TSI | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA20752 | hp2 | a0002 | c0002 | t0002 | g0178 | EUR | TSI | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0075 | EUR | TSI | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA20805 | hp2 | a0001 | c0001 | t0003 | g0002 | EUR | TSI | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0095 | AMR | CLM | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG01123 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | CLM | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02109 | hp1 | a0002 | c0002 | t0011 | g0167 | AFR | ACB | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02109 | hp2 | a0002 | c0002 | t0008 | g0215 | AFR | ACB | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02486 | hp1 | a0002 | c0002 | t0001 | g0001 | AFR | ACB | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02486 | hp2 | a0001 | c0001 | t0020 | g0030 | AFR | ACB | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02559 | hp1 | a0001 | c0001 | t0017 | g0062 | AFR | ACB | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG02559 | hp2 | a0001 | c0001 | t0003 | g0107 | AFR | ACB | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG03471 | hp1 | a0001 | c0001 | t0014 | g0008 | AFR | MSL | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG03471 | hp2 | a0001 | c0001 | t0011 | g0032 | AFR | MSL | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG06807 | hp1 | a0001 | c0001 | t0011 | g0089 | AFR | USA | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| HG06807 | hp2 | a0002 | c0002 | t0002 | g0003 | AFR | USA | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18955 | hp1 | a0001 | c0001 | t0007 | g0004 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA18955 | hp2 | a0002 | c0002 | t0009 | g0006 | EAS | JPT | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA20300 | hp1 | a0002 | c0002 | t0001 | g0018 | AFR | USA | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA20300 | hp2 | a0001 | c0001 | t0010 | g0010 | AFR | USA | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA21309 | hp1 | a0002 | c0002 | t0001 | g0001 | AFR | LWK | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| NA21309 | hp2 | a0001 | c0001 | t0010 | g0010 | AFR | LWK | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0032 | g0063 | REF | REF | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0010 | g0015 | REF | REF | HACD4_chr9_20994509_21036640 | HACD4 | chr9 | 20994509 | 21036640 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:21008059 | G | A | 1 | a0006 | 1 | NA18972.hp2 | missense_variant | MODERATE | c.578C>T | p.Pro193Leu | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 6/7 | 628/8277 | 578/699 | 193/232 | chr9 | 21008059 | |||
| chr9:21015926 | C | T | 1 | a0004 | 1 | HG01255.hp1 | missense_variant | MODERATE | c.355G>A | p.Val119Ile | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 4/7 | 405/8277 | 355/699 | 119/232 | chr9 | 21015926 | |||
| chr9:21015934 | A | G | 1 | a0005 | 1 | NA18612.hp1 | missense_variant | MODERATE | c.347T>C | p.Val116Ala | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 4/7 | 397/8277 | 347/699 | 116/232 | chr9 | 21015934 | |||
| chr9:21016010 | G | A | 1 | a0003 | 1 | HG00733.hp2 | missense_variant&splice_region_variant | MODERATE | c.271C>T | p.Leu91Phe | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 4/7 | 321/8277 | 271/699 | 91/232 | chr9 | 21016010 | |||
| chr9:21029331 | T | C | 3 | a0002 a0005 a0006 |
188 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(185): Show |
missense_variant | MODERATE | c.106A>G | p.Thr36Ala | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 2/7 | 156/8277 | 106/699 | 36/232 | chr9 | 21029331 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:21015948 | T | C | 1 | a0001c0005 | 1 | HG02280.hp2 | synonymous_variant | LOW | c.333A>G | p.Lys111Lys | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 4/7 | 383/8277 | 333/699 | 111/232 | chr9 | 21015948 | |||
| chr9:21029383 | C | T | 1 | a0002c0003 | 3 | HG00408.hp1 NA18960.hp1 NA18964.hp1 |
synonymous_variant | LOW | c.54G>A | p.Ala18Ala | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 2/7 | 104/8277 | 54/699 | 18/232 | chr9 | 21029383 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:20999558 | A | G | 1 | a0001c0001t0051 | 1 | NA18943.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7479T>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 7/7 | 7479 | chr9 | 20999558 | ||||||
| chr9:20999625 | G | GT | 54 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(51): Show |
341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
3_prime_UTR_variant | MODIFIER | c.*7411dupA | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 7/7 | 7411 | chr9 | 20999625 | ||||||
| chr9:20999647 | G | A | 36 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(33): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
3_prime_UTR_variant | MODIFIER | c.*7390C>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 7/7 | 7390 | chr9 | 20999647 | ||||||
| chr9:20999739 | A | G | 1 | a0002c0003t0040 | 1 | HG00408.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7298T>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 7/7 | 7298 | chr9 | 20999739 | ||||||
| chr9:20999771 | T | C | 28 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0012 others(25): Show |
185 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(182): Show |
3_prime_UTR_variant | MODIFIER | c.*7266A>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 7/7 | 7266 | chr9 | 20999771 | ||||||
| chr9:20999806 | ACAAAACG others(116): Show |
A | 1 | a0001c0001t0018 | 3 | HG02572.hp2 HG02970.hp1 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*7108_*7230del | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 7/7 | 7108 | chr9 | 20999806 | ||||||
| chr9:20999812 | C | T | 1 | a0001c0001t0020 | 3 | HG02486.hp2 HG03195.hp1 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*7225G>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 7/7 | 7225 | chr9 | 20999812 | ||||||
| chr9:20999947 | A | G | 1 | a0001c0001t0039 | 1 | HG02683.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7090T>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 7/7 | 7090 | chr9 | 20999947 | ||||||
| chr9:21000097 | T | A | 1 | a0002c0002t0041 | 1 | NA18980.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6940A>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 7/7 | 6940 | chr9 | 21000097 | ||||||
| chr9:21000326 | C | T | 1 | a0001c0001t0053 | 1 | HG02258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6711G>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 7/7 | 6711 | chr9 | 21000326 | ||||||
| chr9:21000496 | G | T | 7 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0021 others(4): Show |
68 | HG00140.hp2 HG00280.hp1 HG00621.hp2 others(65): Show |
3_prime_UTR_variant | MODIFIER | c.*6541C>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 7/7 | 6541 | chr9 | 21000496 | ||||||
| chr9:21000621 | C | G | 5 | a0001c0001t0011 a0001c0001t0036 a0002c0002t0011 others(2): Show |
15 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*6416G>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 7/7 | 6416 | chr9 | 21000621 | ||||||
| chr9:21000648 | A | T | 1 | a0002c0002t0023 | 2 | NA18973.hp2 NA18974.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6389T>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 7/7 | 6389 | chr9 | 21000648 | ||||||
| chr9:21000674 | C | T | 1 | a0002c0002t0044 | 1 | NA19072.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6363G>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 7/7 | 6363 | chr9 | 21000674 | ||||||
| chr9:21000738 | A | G | 54 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(51): Show |
341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
3_prime_UTR_variant | MODIFIER | c.*6299T>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 7/7 | 6299 | chr9 | 21000738 | ||||||
| chr9:21000840 | C | A | 1 | a0001c0001t0024 | 2 | HG01070.hp1 HG01071.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6197G>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 7/7 | 6197 | chr9 | 21000840 | ||||||
| chr9:21000901 | A | G | 1 | a0002c0002t0008 | 14 | HG01261.hp2 HG02055.hp2 HG02109.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*6136T>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 7/7 | 6136 | chr9 | 21000901 | ||||||
| chr9:21000922 | C | G | 1 | a0001c0001t0020 | 3 | HG02486.hp2 HG03195.hp1 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6115G>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 7/7 | 6115 | chr9 | 21000922 | ||||||
| chr9:21000997 | C | T | 1 | a0002c0002t0043 | 1 | HG01346.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6040G>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 7/7 | 6040 | chr9 | 21000997 | ||||||
| chr9:21001428 | G | T | 2 | a0001c0001t0037 a0001c0001t0052 |
2 | HG02896.hp1 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5609C>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 7/7 | 5609 | chr9 | 21001428 | ||||||
| chr9:21001644 | A | T | 1 | a0001c0001t0013 | 10 | HG00735.hp1 HG01081.hp2 HG01255.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*5393T>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 7/7 | 5393 | chr9 | 21001644 | ||||||
| chr9:21002226 | A | C | 13 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0014 others(10): Show |
72 | HG00140.hp2 HG00280.hp1 HG00621.hp2 others(69): Show |
3_prime_UTR_variant | MODIFIER | c.*4811T>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 7/7 | 4811 | chr9 | 21002226 | ||||||
| chr9:21002426 | C | T | 1 | a0001c0001t0021 | 2 | NA18974.hp1 NA19054.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4611G>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 7/7 | 4611 | chr9 | 21002426 | ||||||
| chr9:21002427 | A | G | 61 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(58): Show |
406 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(403): Show |
3_prime_UTR_variant | MODIFIER | c.*4610T>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 7/7 | 4610 | chr9 | 21002427 | ||||||
| chr9:21002458 | C | T | 12 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0014 others(9): Show |
69 | HG00140.hp2 HG00280.hp1 HG00621.hp2 others(66): Show |
3_prime_UTR_variant | MODIFIER | c.*4579G>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 7/7 | 4579 | chr9 | 21002458 | ||||||
| chr9:21002635 | A | G | 13 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0014 others(10): Show |
72 | HG00140.hp2 HG00280.hp1 HG00621.hp2 others(69): Show |
3_prime_UTR_variant | MODIFIER | c.*4402T>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 7/7 | 4402 | chr9 | 21002635 | ||||||
| chr9:21002798 | T | C | 1 | a0001c0001t0034 | 1 | HG00408.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4239A>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 7/7 | 4239 | chr9 | 21002798 | ||||||
| chr9:21002804 | A | C | 1 | a0002c0002t0042 | 1 | NA18963.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4233T>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 7/7 | 4233 | chr9 | 21002804 | ||||||
| chr9:21002869 | G | A | 1 | a0001c0001t0020 | 3 | HG02486.hp2 HG03195.hp1 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4168C>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 7/7 | 4168 | chr9 | 21002869 | ||||||
| chr9:21002869 | G | C | 1 | a0001c0001t0045 | 1 | HG01358.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4168C>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 7/7 | 4168 | chr9 | 21002869 | ||||||
| chr9:21003373 | G | A | 16 | a0001c0001t0001 a0001c0001t0045 a0002c0002t0001 others(13): Show |
87 | HG00099.hp2 HG00438.hp2 HG00558.hp2 others(84): Show |
3_prime_UTR_variant | MODIFIER | c.*3664C>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 7/7 | 3664 | chr9 | 21003373 | ||||||
| chr9:21003407 | T | A | 1 | a0001c0001t0030 | 1 | HG01099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3630A>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 7/7 | 3630 | chr9 | 21003407 | ||||||
| chr9:21003524 | A | G | 1 | a0001c0001t0036 | 1 | HG02257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3513T>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 7/7 | 3513 | chr9 | 21003524 | ||||||
| chr9:21003595 | T | C | 1 | a0002c0002t0046 | 1 | NA19078.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3442A>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 7/7 | 3442 | chr9 | 21003595 | ||||||
| chr9:21003628 | A | G | 1 | a0001c0001t0020 | 3 | HG02486.hp2 HG03195.hp1 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3409T>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 7/7 | 3409 | chr9 | 21003628 | ||||||
| chr9:21003764 | TCA | T | 2 | a0001c0001t0025 a0001c0001t0051 |
3 | HG02071.hp2 NA18943.hp2 NA18967.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3271_*3272delTG | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 7/7 | 3271 | chr9 | 21003764 | ||||||
| chr9:21003784 | C | T | 8 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0016 others(5): Show |
58 | HG00140.hp2 HG00280.hp1 HG00621.hp2 others(55): Show |
3_prime_UTR_variant | MODIFIER | c.*3253G>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 7/7 | 3253 | chr9 | 21003784 | ||||||
| chr9:21004245 | G | A | 10 | a0001c0001t0004 a0001c0001t0007 a0001c0001t0013 others(7): Show |
72 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(69): Show |
3_prime_UTR_variant | MODIFIER | c.*2792C>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 7/7 | 2792 | chr9 | 21004245 | ||||||
| chr9:21004248 | C | G | 1 | a0001c0001t0024 | 2 | HG01070.hp1 HG01071.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2789G>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 7/7 | 2789 | chr9 | 21004248 | ||||||
| chr9:21004398 | A | T | 1 | a0001c0001t0035 | 1 | NA18969.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2639T>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 7/7 | 2639 | chr9 | 21004398 | ||||||
| chr9:21004556 | G | A | 1 | a0001c0001t0024 | 2 | HG01070.hp1 HG01071.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2481C>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 7/7 | 2481 | chr9 | 21004556 | ||||||
| chr9:21004675 | T | C | 1 | a0001c0001t0031 | 1 | HG00280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2362A>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 7/7 | 2362 | chr9 | 21004675 | ||||||
| chr9:21004769 | C | G | 12 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0014 others(9): Show |
71 | HG00140.hp2 HG00280.hp1 HG00621.hp2 others(68): Show |
3_prime_UTR_variant | MODIFIER | c.*2268G>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 7/7 | 2268 | chr9 | 21004769 | ||||||
| chr9:21004802 | T | C | 1 | a0002c0002t0047 | 1 | HG02602.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2235A>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 7/7 | 2235 | chr9 | 21004802 | ||||||
| chr9:21004883 | T | C | 1 | a0002c0002t0048 | 1 | NA19074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2154A>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 7/7 | 2154 | chr9 | 21004883 | ||||||
| chr9:21004994 | G | A | 1 | a0002c0002t0049 | 1 | NA19084.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2043C>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 7/7 | 2043 | chr9 | 21004994 | ||||||
| chr9:21005306 | G | C | 12 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0014 others(9): Show |
71 | HG00140.hp2 HG00280.hp1 HG00621.hp2 others(68): Show |
3_prime_UTR_variant | MODIFIER | c.*1731C>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 7/7 | 1731 | chr9 | 21005306 | ||||||
| chr9:21005366 | G | A | 1 | a0002c0002t0050 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1671C>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 7/7 | 1671 | chr9 | 21005366 | ||||||
| chr9:21005398 | A | C | 12 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0014 others(9): Show |
71 | HG00140.hp2 HG00280.hp1 HG00621.hp2 others(68): Show |
3_prime_UTR_variant | MODIFIER | c.*1639T>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 7/7 | 1639 | chr9 | 21005398 | ||||||
| chr9:21005423 | G | A | 12 | a0001c0001t0004 a0001c0001t0007 a0001c0001t0013 others(9): Show |
76 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(73): Show |
3_prime_UTR_variant | MODIFIER | c.*1614C>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 7/7 | 1614 | chr9 | 21005423 | ||||||
| chr9:21005476 | T | C | 2 | a0001c0001t0005 a0001c0001t0021 |
28 | HG00140.hp2 HG00621.hp2 HG00738.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*1561A>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 7/7 | 1561 | chr9 | 21005476 | ||||||
| chr9:21005491 | A | G | 1 | a0001c0001t0055 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1546T>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 7/7 | 1546 | chr9 | 21005491 | ||||||
| chr9:21005739 | G | A | 1 | a0002c0002t0026 | 2 | HG02615.hp1 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1298C>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 7/7 | 1298 | chr9 | 21005739 | ||||||
| chr9:21005745 | C | T | 12 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0014 others(9): Show |
71 | HG00140.hp2 HG00280.hp1 HG00621.hp2 others(68): Show |
3_prime_UTR_variant | MODIFIER | c.*1292G>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 7/7 | 1292 | chr9 | 21005745 | ||||||
| chr9:21005896 | C | A | 1 | a0002c0002t0033 | 1 | NA18747.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1141G>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 7/7 | 1141 | chr9 | 21005896 | ||||||
| chr9:21005951 | A | G | 2 | a0001c0001t0007 a0001c0001t0034 |
15 | HG00408.hp2 HG00438.hp1 HG03831.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1086T>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 7/7 | 1086 | chr9 | 21005951 | ||||||
| chr9:21006022 | C | T | 12 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0014 others(9): Show |
71 | HG00140.hp2 HG00280.hp1 HG00621.hp2 others(68): Show |
3_prime_UTR_variant | MODIFIER | c.*1015G>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 7/7 | 1015 | chr9 | 21006022 | ||||||
| chr9:21006115 | T | C | 1 | a0002c0002t0054 | 1 | HG02080.hp1 | 3_prime_UTR_variant | MODIFIER | c.*922A>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 7/7 | 922 | chr9 | 21006115 | ||||||
| chr9:21006400 | C | T | 1 | a0002c0002t0022 | 2 | HG02135.hp2 NA18942.hp1 |
3_prime_UTR_variant | MODIFIER | c.*637G>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 7/7 | 637 | chr9 | 21006400 | ||||||
| chr9:21006415 | C | G | 1 | a0002c0002t0033 | 1 | NA18747.hp1 | 3_prime_UTR_variant | MODIFIER | c.*622G>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 7/7 | 622 | chr9 | 21006415 | ||||||
| chr9:21006454 | C | T | 1 | a0001c0001t0017 | 3 | HG02559.hp1 HG02717.hp1 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*583G>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 7/7 | 583 | chr9 | 21006454 | ||||||
| chr9:21006601 | C | A | 12 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0014 others(9): Show |
71 | HG00140.hp2 HG00280.hp1 HG00621.hp2 others(68): Show |
3_prime_UTR_variant | MODIFIER | c.*436G>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 7/7 | 436 | chr9 | 21006601 | ||||||
| chr9:21006935 | A | G | 9 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0016 others(6): Show |
59 | HG00140.hp2 HG00280.hp1 HG00621.hp2 others(56): Show |
3_prime_UTR_variant | MODIFIER | c.*102T>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 7/7 | 102 | chr9 | 21006935 | ||||||
| chr9:21006959 | C | G | 1 | a0001c0001t0027 | 1 | HG01433.hp1 | 3_prime_UTR_variant | MODIFIER | c.*78G>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 7/7 | 78 | chr9 | 21006959 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:21007318 | T | C | 1 | a0001c0001t0017g0062 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.617-199A>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 6/6 | chr9 | 21007318 | |||||||
| chr9:21007384 | C | T | 2 | a0001c0001t0014g0008 a0001c0001t0014g0110 |
8 | HG00639.hp1 HG00642.hp1 HG01069.hp1 others(5): Show |
intron_variant | MODIFIER | c.617-265G>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 6/6 | chr9 | 21007384 | |||||||
| chr9:21007608 | C | T | 2 | a0002c0002t0008g0215 a0002c0002t0038g0216 |
2 | HG01884.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.616+413G>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 6/6 | chr9 | 21007608 | |||||||
| chr9:21007633 | C | T | 234 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0002g0037 others(231): Show |
418 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(415): Show |
intron_variant | MODIFIER | c.616+388G>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 6/6 | chr9 | 21007633 | |||||||
| chr9:21007760 | A | C | 7 | a0001c0001t0012g0023 a0001c0001t0012g0152 a0001c0001t0012g0153 others(4): Show |
9 | HG03669.hp2 NA18945.hp2 NA18960.hp2 others(6): Show |
intron_variant | MODIFIER | c.616+261T>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 6/6 | chr9 | 21007760 | |||||||
| chr9:21007762 | A | G | 2 | a0002c0003t0001g0172 a0002c0003t0001g0173 |
2 | NA18960.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.616+259T>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 6/6 | chr9 | 21007762 | |||||||
| chr9:21007766 | C | A | 5 | a0002c0002t0001g0017 a0002c0002t0001g0053 a0002c0002t0001g0218 others(2): Show |
9 | HG00558.hp2 NA18939.hp2 NA18949.hp2 others(6): Show |
intron_variant | MODIFIER | c.616+255G>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 6/6 | chr9 | 21007766 | |||||||
| chr9:21007936 | A | G | 197 | a0001c0001t0002g0037 a0001c0001t0002g0097 a0001c0001t0002g0108 others(194): Show |
343 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(340): Show |
intron_variant | MODIFIER | c.616+85T>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 6/6 | chr9 | 21007936 | |||||||
| chr9:21007959 | C | T | 4 | a0002c0002t0001g0017 a0002c0002t0001g0218 a0002c0002t0001g0232 others(1): Show |
7 | HG00558.hp2 NA18939.hp2 NA18949.hp2 others(4): Show |
intron_variant | MODIFIER | c.616+62G>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 6/6 | chr9 | 21007959 | |||||||
| chr9:21008378 | T | C | 151 | a0001c0001t0002g0037 a0001c0001t0002g0117 a0001c0001t0002g0123 others(148): Show |
267 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(264): Show |
intron_variant | MODIFIER | c.491-232A>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 5/6 | chr9 | 21008378 | |||||||
| chr9:21008391 | G | T | 1 | a0001c0001t0004g0132 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.491-245C>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 5/6 | chr9 | 21008391 | |||||||
| chr9:21008415 | T | C | 1 | a0002c0002t0002g0224 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.491-269A>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 5/6 | chr9 | 21008415 | |||||||
| chr9:21008417 | A | G | 35 | a0001c0001t0002g0140 a0001c0001t0003g0124 a0002c0002t0001g0190 others(32): Show |
60 | HG00280.hp2 HG00544.hp2 HG00735.hp2 others(57): Show |
intron_variant | MODIFIER | c.491-271T>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 5/6 | chr9 | 21008417 | |||||||
| chr9:21008535 | C | T | 1 | a0001c0001t0006g0076 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.491-389G>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 5/6 | chr9 | 21008535 | |||||||
| chr9:21008580 | G | A | 2 | a0001c0001t0020g0030 a0001c0001t0020g0085 |
3 | HG02486.hp2 HG03195.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.491-434C>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 5/6 | chr9 | 21008580 | |||||||
| chr9:21008581 | C | A | 1 | a0002c0002t0033g0202 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.491-435G>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 5/6 | chr9 | 21008581 | |||||||
| chr9:21008713 | A | C | 1 | a0001c0001t0055g0161 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.491-567T>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 5/6 | chr9 | 21008713 | |||||||
| chr9:21008726 | A | G | 138 | a0001c0001t0002g0037 a0001c0001t0002g0117 a0001c0001t0002g0123 others(135): Show |
251 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(248): Show |
intron_variant | MODIFIER | c.491-580T>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 5/6 | chr9 | 21008726 | |||||||
| chr9:21009192 | G | A | 106 | a0001c0001t0002g0140 a0001c0001t0003g0124 a0002c0002t0001g0001 others(103): Show |
181 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(178): Show |
intron_variant | MODIFIER | c.491-1046C>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 5/6 | chr9 | 21009192 | |||||||
| chr9:21009280 | T | C | 1 | a0001c0001t0005g0071 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.491-1134A>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 5/6 | chr9 | 21009280 | |||||||
| chr9:21009285 | A | G | 1 | a0002c0002t0008g0054 | 2 | HG02895.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.491-1139T>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 5/6 | chr9 | 21009285 | |||||||
| chr9:21009404 | G | A | 2 | a0001c0001t0013g0040 a0001c0001t0013g0041 |
4 | HG02055.hp1 HG02818.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.491-1258C>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 5/6 | chr9 | 21009404 | |||||||
| chr9:21009466 | C | T | 1 | a0001c0001t0011g0094 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.491-1320G>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 5/6 | chr9 | 21009466 | |||||||
| chr9:21009661 | G | A | 240 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0002g0037 others(237): Show |
420 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(417): Show |
intron_variant | MODIFIER | c.491-1515C>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 5/6 | chr9 | 21009661 | |||||||
| chr9:21009744 | C | G | 1 | a0002c0002t0015g0050 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.491-1598G>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 5/6 | chr9 | 21009744 | |||||||
| chr9:21009747 | G | C | 1 | a0001c0001t0004g0106 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.491-1601C>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 5/6 | chr9 | 21009747 | |||||||
| chr9:21009803 | A | C | 229 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0002g0037 others(226): Show |
401 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(398): Show |
intron_variant | MODIFIER | c.491-1657T>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 5/6 | chr9 | 21009803 | |||||||
| chr9:21010038 | C | A | 7 | a0001c0001t0012g0023 a0001c0001t0012g0152 a0001c0001t0012g0153 others(4): Show |
9 | HG03669.hp2 NA18945.hp2 NA18960.hp2 others(6): Show |
intron_variant | MODIFIER | c.490+1551G>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 5/6 | chr9 | 21010038 | |||||||
| chr9:21010114 | G | A | 229 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0002g0037 others(226): Show |
401 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(398): Show |
intron_variant | MODIFIER | c.490+1475C>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 5/6 | chr9 | 21010114 | |||||||
| chr9:21010170 | A | G | 3 | a0001c0001t0011g0032 a0001c0001t0011g0090 a0001c0001t0011g0091 |
4 | HG01891.hp1 HG02922.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.490+1419T>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 5/6 | chr9 | 21010170 | |||||||
| chr9:21010441 | C | G | 1 | a0001c0001t0003g0107 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.490+1148G>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 5/6 | chr9 | 21010441 | |||||||
| chr9:21010456 | A | ACCC | 13 | a0001c0001t0001g0075 a0001c0001t0005g0005 a0001c0001t0005g0064 others(10): Show |
24 | HG00741.hp2 HG01934.hp1 HG02257.hp2 others(21): Show |
intron_variant | MODIFIER | c.490+1130_490+1132d others(5): Show |
HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 5/6 | chr9 | 21010456 | |||||||
| chr9:21010456 | A | ACCCC | 12 | a0001c0001t0001g0074 a0001c0001t0005g0027 a0001c0001t0005g0068 others(9): Show |
21 | HG00099.hp2 HG00621.hp2 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.490+1129_490+1132d others(6): Show |
HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 5/6 | chr9 | 21010456 | |||||||
| chr9:21010456 | A | AT | 13 | a0001c0001t0002g0097 a0001c0001t0004g0009 a0001c0001t0004g0012 others(10): Show |
38 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(35): Show |
intron_variant | MODIFIER | c.490+1132_490+1133i others(3): Show |
HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 5/6 | chr9 | 21010456 | |||||||
| chr9:21010456 | A | ATC | 17 | a0001c0001t0002g0108 a0001c0001t0004g0038 a0001c0001t0004g0098 others(14): Show |
21 | HG00438.hp1 HG00735.hp1 HG01081.hp2 others(18): Show |
intron_variant | MODIFIER | c.490+1132_490+1133i others(4): Show |
HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 5/6 | chr9 | 21010456 | |||||||
| chr9:21010456 | A | ATCC | 13 | a0001c0001t0002g0109 a0001c0001t0004g0086 a0001c0001t0004g0093 others(10): Show |
13 | HG01243.hp2 HG01255.hp2 HG01516.hp1 others(10): Show |
intron_variant | MODIFIER | c.490+1132_490+1133i others(5): Show |
HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 5/6 | chr9 | 21010456 | |||||||
| chr9:21010456 | A | ATCCC | 2 | a0001c0001t0018g0034 a0001c0001t0055g0161 |
3 | HG02451.hp1 HG02572.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.490+1132_490+1133i others(6): Show |
HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 5/6 | chr9 | 21010456 | |||||||
| chr9:21010456 | ACC | A | 131 | a0001c0001t0002g0037 a0001c0001t0002g0117 a0001c0001t0002g0123 others(128): Show |
245 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(242): Show |
intron_variant | MODIFIER | c.490+1131_490+1132d others(4): Show |
HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 5/6 | chr9 | 21010456 | |||||||
| chr9:21010457 | C | T | 7 | a0001c0001t0012g0023 a0001c0001t0012g0152 a0001c0001t0012g0153 others(4): Show |
9 | HG03669.hp2 NA18945.hp2 NA18960.hp2 others(6): Show |
intron_variant | MODIFIER | c.490+1132G>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 5/6 | chr9 | 21010457 | |||||||
| chr9:21010458 | C | A | 2 | a0001c0001t0014g0008 a0001c0001t0014g0110 |
4 | HG00639.hp1 HG00642.hp1 HG01069.hp1 others(1): Show |
intron_variant | MODIFIER | c.490+1131G>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 5/6 | chr9 | 21010458 | |||||||
| chr9:21010462 | C | G | 1 | a0002c0002t0008g0054 | 2 | HG02895.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.490+1127G>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 5/6 | chr9 | 21010462 | |||||||
| chr9:21010465 | C | G | 31 | a0001c0001t0002g0037 a0001c0001t0002g0117 a0001c0001t0002g0123 others(28): Show |
68 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(65): Show |
intron_variant | MODIFIER | c.490+1124G>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 5/6 | chr9 | 21010465 | |||||||
| chr9:21010466 | C | G | 1 | a0001c0001t0013g0136 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.490+1123G>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 5/6 | chr9 | 21010466 | |||||||
| chr9:21010467 | C | G | 108 | a0001c0001t0002g0140 a0001c0001t0003g0124 a0001c0001t0006g0028 others(105): Show |
185 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(182): Show |
intron_variant | MODIFIER | c.490+1122G>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 5/6 | chr9 | 21010467 | |||||||
| chr9:21010469 | C | A | 31 | a0001c0001t0002g0037 a0001c0001t0002g0117 a0001c0001t0002g0123 others(28): Show |
68 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(65): Show |
intron_variant | MODIFIER | c.490+1120G>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 5/6 | chr9 | 21010469 | |||||||
| chr9:21010614 | C | A | 1 | a0001c0001t0055g0161 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.490+975G>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 5/6 | chr9 | 21010614 | |||||||
| chr9:21010624 | G | A | 46 | a0001c0001t0002g0097 a0001c0001t0002g0108 a0001c0001t0002g0109 others(43): Show |
76 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(73): Show |
intron_variant | MODIFIER | c.490+965C>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 5/6 | chr9 | 21010624 | |||||||
| chr9:21010877 | G | A | 1 | a0002c0002t0001g0048 | 2 | HG02074.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.490+712C>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 5/6 | chr9 | 21010877 | |||||||
| chr9:21010905 | C | T | 1 | a0001c0001t0004g0106 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.490+684G>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 5/6 | chr9 | 21010905 | |||||||
| chr9:21011017 | G | A | 9 | a0001c0001t0004g0009 a0001c0001t0004g0126 a0001c0001t0004g0129 others(6): Show |
25 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(22): Show |
intron_variant | MODIFIER | c.490+572C>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 5/6 | chr9 | 21011017 | |||||||
| chr9:21011188 | G | T | 1 | a0001c0001t0053g0148 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.490+401C>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 5/6 | chr9 | 21011188 | |||||||
| chr9:21011288 | T | C | 89 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0002g0097 others(86): Show |
148 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(145): Show |
intron_variant | MODIFIER | c.490+301A>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 5/6 | chr9 | 21011288 | |||||||
| chr9:21011723 | A | G | 9 | a0001c0001t0011g0094 a0001c0001t0012g0023 a0001c0001t0012g0152 others(6): Show |
11 | HG02451.hp1 HG03669.hp2 NA18945.hp2 others(8): Show |
intron_variant | MODIFIER | c.384-28T>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 4/6 | chr9 | 21011723 | |||||||
| chr9:21011834 | G | C | 31 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0005g0005 others(28): Show |
57 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(54): Show |
intron_variant | MODIFIER | c.384-139C>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 4/6 | chr9 | 21011834 | |||||||
| chr9:21012028 | G | A | 3 | a0002c0002t0002g0026 a0002c0002t0002g0178 a0002c0002t0002g0179 |
5 | HG00280.hp2 HG01256.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.384-333C>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 4/6 | chr9 | 21012028 | |||||||
| chr9:21012171 | G | A | 139 | a0001c0001t0002g0037 a0001c0001t0002g0117 a0001c0001t0002g0123 others(136): Show |
252 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(249): Show |
intron_variant | MODIFIER | c.384-476C>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 4/6 | chr9 | 21012171 | |||||||
| chr9:21012227 | C | T | 1 | a0001c0001t0003g0107 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.384-532G>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 4/6 | chr9 | 21012227 | |||||||
| chr9:21012326 | A | G | 1 | a0001c0001t0003g0120 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.384-631T>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 4/6 | chr9 | 21012326 | |||||||
| chr9:21012448 | C | A | 26 | a0001c0001t0002g0140 a0002c0002t0001g0190 a0002c0002t0002g0003 others(23): Show |
47 | HG00280.hp2 HG00735.hp2 HG01069.hp2 others(44): Show |
intron_variant | MODIFIER | c.384-753G>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 4/6 | chr9 | 21012448 | |||||||
| chr9:21012746 | G | A | 139 | a0001c0001t0002g0037 a0001c0001t0002g0117 a0001c0001t0002g0123 others(136): Show |
252 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(249): Show |
intron_variant | MODIFIER | c.384-1051C>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 4/6 | chr9 | 21012746 | |||||||
| chr9:21012788 | C | T | 45 | a0001c0001t0002g0097 a0001c0001t0002g0158 a0001c0001t0004g0009 others(42): Show |
75 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(72): Show |
intron_variant | MODIFIER | c.384-1093G>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 4/6 | chr9 | 21012788 | |||||||
| chr9:21012792 | G | T | 1 | a0001c0001t0011g0094 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.384-1097C>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 4/6 | chr9 | 21012792 | |||||||
| chr9:21012829 | G | A | 1 | a0001c0001t0055g0161 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.384-1134C>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 4/6 | chr9 | 21012829 | |||||||
| chr9:21012882 | C | T | 1 | a0002c0002t0002g0061 | 2 | NA19009.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.384-1187G>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 4/6 | chr9 | 21012882 | |||||||
| chr9:21012901 | C | T | 242 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0002g0037 others(239): Show |
422 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(419): Show |
intron_variant | MODIFIER | c.384-1206G>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 4/6 | chr9 | 21012901 | |||||||
| chr9:21012935 | C | T | 7 | a0001c0001t0012g0023 a0001c0001t0012g0152 a0001c0001t0012g0153 others(4): Show |
9 | HG03669.hp2 NA18945.hp2 NA18960.hp2 others(6): Show |
intron_variant | MODIFIER | c.384-1240G>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 4/6 | chr9 | 21012935 | |||||||
| chr9:21012936 | G | A | 29 | a0001c0001t0002g0037 a0001c0001t0002g0117 a0001c0001t0002g0123 others(26): Show |
64 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(61): Show |
intron_variant | MODIFIER | c.384-1241C>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 4/6 | chr9 | 21012936 | |||||||
| chr9:21012994 | G | T | 1 | a0001c0001t0003g0119 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.384-1299C>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 4/6 | chr9 | 21012994 | |||||||
| chr9:21013066 | C | CA | 13 | a0001c0001t0004g0131 a0001c0001t0013g0039 a0001c0001t0013g0040 others(10): Show |
17 | HG00735.hp1 HG01081.hp2 HG01099.hp1 others(14): Show |
intron_variant | MODIFIER | c.384-1372dupT | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 4/6 | chr9 | 21013066 | |||||||
| chr9:21013238 | T | C | 1 | a0001c0001t0011g0089 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.384-1543A>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 4/6 | chr9 | 21013238 | |||||||
| chr9:21013244 | G | A | 1 | a0002c0002t0001g0243 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.384-1549C>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 4/6 | chr9 | 21013244 | |||||||
| chr9:21013246 | G | T | 2 | a0002c0002t0008g0215 a0002c0002t0038g0216 |
2 | HG01884.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.384-1551C>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 4/6 | chr9 | 21013246 | |||||||
| chr9:21013479 | C | G | 35 | a0001c0001t0002g0158 a0001c0001t0004g0009 a0001c0001t0004g0012 others(32): Show |
64 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(61): Show |
intron_variant | MODIFIER | c.384-1784G>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 4/6 | chr9 | 21013479 | |||||||
| chr9:21013517 | G | T | 16 | a0002c0002t0001g0168 a0002c0002t0008g0051 a0002c0002t0008g0054 others(13): Show |
29 | HG01261.hp2 HG02055.hp2 HG02258.hp1 others(26): Show |
intron_variant | MODIFIER | c.384-1822C>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 4/6 | chr9 | 21013517 | |||||||
| chr9:21013593 | G | T | 1 | a0001c0001t0011g0094 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.384-1898C>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 4/6 | chr9 | 21013593 | |||||||
| chr9:21013663 | T | C | 1 | a0001c0001t0013g0041 | 2 | HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.384-1968A>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 4/6 | chr9 | 21013663 | |||||||
| chr9:21013743 | A | C | 241 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0002g0037 others(238): Show |
421 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(418): Show |
intron_variant | MODIFIER | c.384-2048T>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 4/6 | chr9 | 21013743 | |||||||
| chr9:21013799 | T | C | 1 | a0002c0003t0040g0142 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.383+2099A>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 4/6 | chr9 | 21013799 | |||||||
| chr9:21013903 | A | G | 2 | a0001c0001t0013g0039 a0001c0001t0013g0134 |
3 | HG01081.hp2 HG01516.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.383+1995T>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 4/6 | chr9 | 21013903 | |||||||
| chr9:21013906 | C | G | 6 | a0001c0001t0004g0086 a0001c0001t0004g0106 a0001c0001t0018g0034 others(3): Show |
7 | HG02572.hp2 HG02896.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.383+1992G>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 4/6 | chr9 | 21013906 | |||||||
| chr9:21013969 | G | T | 1 | a0002c0002t0002g0192 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.383+1929C>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 4/6 | chr9 | 21013969 | |||||||
| chr9:21013978 | T | C | 1 | a0002c0002t0002g0192 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.383+1920A>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 4/6 | chr9 | 21013978 | |||||||
| chr9:21013983 | C | G | 1 | a0002c0002t0002g0192 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.383+1915G>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 4/6 | chr9 | 21013983 | |||||||
| chr9:21013986 | G | A | 1 | a0002c0002t0002g0192 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.383+1912C>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 4/6 | chr9 | 21013986 | |||||||
| chr9:21013987 | C | T | 1 | a0002c0002t0002g0192 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.383+1911G>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 4/6 | chr9 | 21013987 | |||||||
| chr9:21013988 | A | G | 1 | a0002c0002t0002g0192 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.383+1910T>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 4/6 | chr9 | 21013988 | |||||||
| chr9:21013989 | A | T | 1 | a0002c0002t0002g0192 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.383+1909T>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 4/6 | chr9 | 21013989 | |||||||
| chr9:21013990 | G | T | 1 | a0002c0002t0002g0192 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.383+1908C>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 4/6 | chr9 | 21013990 | |||||||
| chr9:21014004 | G | A | 73 | a0002c0002t0001g0001 a0002c0002t0001g0017 a0002c0002t0001g0018 others(70): Show |
124 | HG00438.hp2 HG00558.hp2 HG00621.hp1 others(121): Show |
intron_variant | MODIFIER | c.383+1894C>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 4/6 | chr9 | 21014004 | |||||||
| chr9:21014062 | A | T | 1 | a0002c0002t0002g0192 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.383+1836T>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 4/6 | chr9 | 21014062 | |||||||
| chr9:21014077 | T | C | 8 | a0002c0002t0008g0051 a0002c0002t0008g0055 a0002c0002t0008g0056 others(5): Show |
11 | HG01261.hp2 HG02055.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.383+1821A>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 4/6 | chr9 | 21014077 | |||||||
| chr9:21014177 | A | G | 54 | a0002c0002t0001g0001 a0002c0002t0001g0017 a0002c0002t0001g0018 others(51): Show |
92 | HG00438.hp2 HG00558.hp2 HG00621.hp1 others(89): Show |
intron_variant | MODIFIER | c.383+1721T>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 4/6 | chr9 | 21014177 | |||||||
| chr9:21014243 | T | G | 1 | a0002c0002t0001g0221 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.383+1655A>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 4/6 | chr9 | 21014243 | |||||||
| chr9:21014253 | A | G | 4 | a0001c0001t0011g0031 a0001c0001t0011g0087 a0001c0001t0011g0089 others(1): Show |
5 | HG02257.hp2 HG02572.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.383+1645T>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 4/6 | chr9 | 21014253 | |||||||
| chr9:21014357 | C | G | 7 | a0001c0001t0012g0023 a0001c0001t0012g0152 a0001c0001t0012g0153 others(4): Show |
9 | HG03669.hp2 NA18945.hp2 NA18960.hp2 others(6): Show |
intron_variant | MODIFIER | c.383+1541G>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 4/6 | chr9 | 21014357 | |||||||
| chr9:21014362 | C | T | 1 | a0002c0002t0001g0194 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.383+1536G>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 4/6 | chr9 | 21014362 | |||||||
| chr9:21014434 | A | G | 3 | a0001c0001t0017g0062 a0001c0001t0017g0100 a0001c0001t0017g0101 |
3 | HG02559.hp1 HG02717.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.383+1464T>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 4/6 | chr9 | 21014434 | |||||||
| chr9:21014436 | T | C | 2 | a0001c0001t0020g0030 a0001c0001t0020g0085 |
3 | HG02486.hp2 HG03195.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.383+1462A>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 4/6 | chr9 | 21014436 | |||||||
| chr9:21014483 | C | G | 89 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0002g0097 others(86): Show |
148 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(145): Show |
intron_variant | MODIFIER | c.383+1415G>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 4/6 | chr9 | 21014483 | |||||||
| chr9:21014540 | T | A | 1 | a0001c0001t0005g0081 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.383+1358A>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 4/6 | chr9 | 21014540 | |||||||
| chr9:21014571 | A | C | 2 | a0001c0001t0020g0030 a0001c0001t0020g0085 |
3 | HG02486.hp2 HG03195.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.383+1327T>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 4/6 | chr9 | 21014571 | |||||||
| chr9:21014601 | T | G | 1 | a0001c0001t0027g0067 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.383+1297A>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 4/6 | chr9 | 21014601 | |||||||
| chr9:21014613 | A | C | 1 | a0002c0002t0002g0192 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.383+1285T>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 4/6 | chr9 | 21014613 | |||||||
| chr9:21014629 | T | C | 111 | a0001c0001t0002g0140 a0001c0001t0003g0124 a0001c0001t0006g0146 others(108): Show |
189 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(186): Show |
intron_variant | MODIFIER | c.383+1269A>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 4/6 | chr9 | 21014629 | |||||||
| chr9:21014690 | G | C | 4 | a0001c0001t0003g0124 a0002c0002t0002g0052 a0002c0002t0002g0163 others(1): Show |
5 | NA18939.hp1 NA18949.hp1 NA18969.hp2 others(2): Show |
intron_variant | MODIFIER | c.383+1208C>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 4/6 | chr9 | 21014690 | |||||||
| chr9:21014700 | T | C | 1 | a0001c0001t0012g0154 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.383+1198A>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 4/6 | chr9 | 21014700 | |||||||
| chr9:21014823 | A | G | 1 | a0001c0001t0003g0107 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.383+1075T>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 4/6 | chr9 | 21014823 | |||||||
| chr9:21014838 | C | A | 1 | a0001c0001t0011g0094 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.383+1060G>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 4/6 | chr9 | 21014838 | |||||||
| chr9:21015113 | T | C | 1 | a0001c0001t0012g0152 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.383+785A>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 4/6 | chr9 | 21015113 | |||||||
| chr9:21015198 | T | C | 1 | a0002c0003t0001g0173 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.383+700A>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 4/6 | chr9 | 21015198 | |||||||
| chr9:21015430 | A | G | 1 | a0001c0001t0014g0110 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.383+468T>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 4/6 | chr9 | 21015430 | |||||||
| chr9:21015624 | A | T | 1 | a0002c0002t0002g0192 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.383+274T>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 4/6 | chr9 | 21015624 | |||||||
| chr9:21015652 | T | G | 76 | a0001c0001t0002g0037 a0001c0001t0002g0097 a0001c0001t0002g0117 others(73): Show |
141 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(138): Show |
intron_variant | MODIFIER | c.383+246A>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 4/6 | chr9 | 21015652 | |||||||
| chr9:21015757 | A | G | 2 | a0002c0002t0001g0177 a0002c0002t0049g0193 |
2 | NA18965.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.383+141T>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 4/6 | chr9 | 21015757 | |||||||
| chr9:21016216 | T | C | 1 | a0001c0001t0055g0161 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.271-206A>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21016216 | |||||||
| chr9:21016366 | A | G | 229 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0002g0037 others(226): Show |
401 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(398): Show |
intron_variant | MODIFIER | c.271-356T>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21016366 | |||||||
| chr9:21016367 | A | G | 1 | a0002c0002t0002g0192 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.271-357T>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21016367 | |||||||
| chr9:21016369 | A | G | 1 | a0001c0001t0003g0174 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.271-359T>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21016369 | |||||||
| chr9:21016375 | G | A | 1 | a0002c0002t0001g0181 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.271-365C>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21016375 | |||||||
| chr9:21016509 | A | G | 2 | a0001c0001t0011g0094 a0001c0001t0055g0161 |
2 | HG02451.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.271-499T>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21016509 | |||||||
| chr9:21016543 | G | A | 2 | a0001c0001t0002g0108 a0001c0001t0002g0109 |
2 | HG01243.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.271-533C>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21016543 | |||||||
| chr9:21016647 | TG | T | 48 | a0002c0002t0001g0001 a0002c0002t0001g0017 a0002c0002t0001g0018 others(45): Show |
84 | HG00438.hp2 HG00558.hp2 HG00621.hp1 others(81): Show |
intron_variant | MODIFIER | c.271-638delC | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21016647 | |||||||
| chr9:21016728 | GT | G | 84 | a0001c0001t0002g0037 a0001c0001t0002g0097 a0001c0001t0002g0117 others(81): Show |
152 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.271-719delA | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21016728 | |||||||
| chr9:21016735 | A | G | 1 | a0001c0001t0055g0161 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.271-725T>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21016735 | |||||||
| chr9:21016767 | T | A | 1 | a0001c0001t0004g0149 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.271-757A>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21016767 | |||||||
| chr9:21016782 | C | CT | 113 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0002g0037 others(110): Show |
206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.271-773dupA | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21016782 | |||||||
| chr9:21016793 | C | T | 1 | a0002c0002t0002g0192 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.271-783G>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21016793 | |||||||
| chr9:21016794 | T | C | 1 | a0002c0002t0002g0192 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.271-784A>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21016794 | |||||||
| chr9:21016930 | C | G | 120 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0002g0037 others(117): Show |
215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.271-920G>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21016930 | |||||||
| chr9:21017241 | A | G | 109 | a0001c0001t0002g0140 a0001c0001t0019g0022 a0002c0002t0001g0001 others(106): Show |
187 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(184): Show |
intron_variant | MODIFIER | c.271-1231T>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21017241 | |||||||
| chr9:21017335 | G | T | 1 | a0001c0001t0002g0117 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.271-1325C>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21017335 | |||||||
| chr9:21017419 | TTATAA | T | 33 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0005g0005 others(30): Show |
60 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(57): Show |
intron_variant | MODIFIER | c.271-1414_271-1410d others(7): Show |
HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21017419 | |||||||
| chr9:21017638 | C | T | 25 | a0001c0001t0004g0009 a0001c0001t0004g0012 a0001c0001t0004g0019 others(22): Show |
53 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(50): Show |
intron_variant | MODIFIER | c.271-1628G>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21017638 | |||||||
| chr9:21017645 | A | C | 89 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0002g0097 others(86): Show |
148 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(145): Show |
intron_variant | MODIFIER | c.271-1635T>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21017645 | |||||||
| chr9:21017690 | G | A | 2 | a0001c0001t0002g0108 a0001c0001t0002g0109 |
2 | HG01243.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.271-1680C>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21017690 | |||||||
| chr9:21017744 | C | T | 199 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0002g0097 others(196): Show |
335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.271-1734G>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21017744 | |||||||
| chr9:21017769 | C | T | 1 | a0001c0001t0011g0094 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.271-1759G>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21017769 | |||||||
| chr9:21017829 | G | A | 71 | a0002c0002t0001g0001 a0002c0002t0001g0017 a0002c0002t0001g0018 others(68): Show |
121 | HG00438.hp2 HG00558.hp2 HG00621.hp1 others(118): Show |
intron_variant | MODIFIER | c.271-1819C>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21017829 | |||||||
| chr9:21017885 | T | C | 110 | a0001c0001t0002g0140 a0001c0001t0019g0022 a0001c0001t0020g0030 others(107): Show |
188 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(185): Show |
intron_variant | MODIFIER | c.271-1875A>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21017885 | |||||||
| chr9:21018048 | A | G | 1 | a0001c0001t0003g0116 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.271-2038T>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21018048 | |||||||
| chr9:21018061 | C | A | 1 | a0001c0001t0019g0022 | 3 | HG01074.hp2 HG02451.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.271-2051G>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21018061 | |||||||
| chr9:21018178 | A | C | 1 | a0001c0001t0004g0103 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.271-2168T>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21018178 | |||||||
| chr9:21018472 | A | C | 85 | a0001c0001t0002g0037 a0001c0001t0002g0097 a0001c0001t0002g0117 others(82): Show |
153 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(150): Show |
intron_variant | MODIFIER | c.271-2462T>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21018472 | |||||||
| chr9:21018529 | C | T | 1 | a0001c0001t0003g0047 | 2 | NA19004.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.271-2519G>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21018529 | |||||||
| chr9:21018551 | G | C | 118 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0002g0037 others(115): Show |
213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): Show |
intron_variant | MODIFIER | c.271-2541C>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21018551 | |||||||
| chr9:21018551 | G | T | 109 | a0001c0001t0002g0140 a0001c0001t0006g0146 a0001c0001t0019g0022 others(106): Show |
186 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(183): Show |
intron_variant | MODIFIER | c.271-2541C>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21018551 | |||||||
| chr9:21018575 | C | T | 30 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0005g0005 others(27): Show |
56 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(53): Show |
intron_variant | MODIFIER | c.271-2565G>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21018575 | |||||||
| chr9:21018592 | C | T | 1 | a0001c0001t0055g0161 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.271-2582G>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21018592 | |||||||
| chr9:21018776 | T | C | 2 | a0001c0001t0002g0095 a0001c0001t0053g0148 |
2 | HG01123.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.271-2766A>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21018776 | |||||||
| chr9:21018812 | C | A | 109 | a0001c0001t0002g0140 a0001c0001t0006g0146 a0001c0001t0019g0022 others(106): Show |
186 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(183): Show |
intron_variant | MODIFIER | c.271-2802G>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21018812 | |||||||
| chr9:21018813 | ATTTTTAT others(1): Show |
A | 109 | a0001c0001t0002g0140 a0001c0001t0006g0146 a0001c0001t0019g0022 others(106): Show |
186 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(183): Show |
intron_variant | MODIFIER | c.271-2811_271-2804d others(10): Show |
HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21018813 | |||||||
| chr9:21018823 | T | C | 109 | a0001c0001t0002g0140 a0001c0001t0006g0146 a0001c0001t0019g0022 others(106): Show |
186 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(183): Show |
intron_variant | MODIFIER | c.271-2813A>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21018823 | |||||||
| chr9:21018919 | G | C | 1 | a0001c0001t0055g0161 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.271-2909C>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21018919 | |||||||
| chr9:21018942 | C | T | 1 | a0001c0001t0011g0094 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.271-2932G>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21018942 | |||||||
| chr9:21019058 | C | T | 1 | a0001c0001t0004g0131 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.271-3048G>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21019058 | |||||||
| chr9:21019124 | C | T | 196 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0002g0097 others(193): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.271-3114G>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21019124 | |||||||
| chr9:21019235 | C | T | 242 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0002g0037 others(239): Show |
422 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(419): Show |
intron_variant | MODIFIER | c.271-3225G>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21019235 | |||||||
| chr9:21019330 | C | A | 1 | a0002c0002t0008g0186 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.271-3320G>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21019330 | |||||||
| chr9:21019379 | T | A | 70 | a0001c0001t0002g0037 a0001c0001t0002g0097 a0001c0001t0002g0117 others(67): Show |
135 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.271-3369A>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21019379 | |||||||
| chr9:21019382 | C | T | 2 | a0001c0001t0002g0108 a0001c0001t0002g0109 |
2 | HG01243.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.271-3372G>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21019382 | |||||||
| chr9:21019449 | C | T | 3 | a0002c0002t0004g0024 a0002c0002t0004g0182 a0002c0002t0004g0239 |
5 | HG00673.hp2 NA18941.hp2 NA18954.hp1 others(2): Show |
intron_variant | MODIFIER | c.271-3439G>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21019449 | |||||||
| chr9:21019488 | G | T | 1 | a0001c0001t0003g0107 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.271-3478C>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21019488 | |||||||
| chr9:21019546 | G | C | 1 | a0001c0001t0003g0107 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.271-3536C>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21019546 | |||||||
| chr9:21019611 | T | A | 1 | a0002c0002t0002g0208 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.271-3601A>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21019611 | |||||||
| chr9:21019645 | A | G | 1 | a0001c0001t0005g0070 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.271-3635T>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21019645 | |||||||
| chr9:21019651 | T | G | 118 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0002g0037 others(115): Show |
213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): Show |
intron_variant | MODIFIER | c.271-3641A>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21019651 | |||||||
| chr9:21019761 | A | C | 3 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0024g0036 |
4 | HG01070.hp1 HG01071.hp2 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.271-3751T>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21019761 | |||||||
| chr9:21019818 | C | T | 113 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0002g0037 others(110): Show |
207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.271-3808G>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21019818 | |||||||
| chr9:21019869 | ATTAT | A | 114 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0002g0037 others(111): Show |
209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.271-3863_271-3860d others(6): Show |
HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21019869 | |||||||
| chr9:21019896 | C | T | 12 | a0001c0001t0005g0005 a0001c0001t0005g0011 a0001c0001t0005g0027 others(9): Show |
26 | HG00140.hp2 HG00621.hp2 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.271-3886G>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21019896 | |||||||
| chr9:21019908 | G | T | 1 | a0001c0001t0003g0107 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.271-3898C>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21019908 | |||||||
| chr9:21019938 | T | C | 1 | a0001c0001t0003g0107 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.271-3928A>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21019938 | |||||||
| chr9:21020067 | A | G | 1 | a0002c0002t0008g0186 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.271-4057T>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21020067 | |||||||
| chr9:21020096 | T | A | 114 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0002g0037 others(111): Show |
209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.271-4086A>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21020096 | |||||||
| chr9:21020115 | T | A | 113 | a0001c0001t0002g0140 a0001c0001t0006g0146 a0001c0001t0019g0022 others(110): Show |
190 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(187): Show |
intron_variant | MODIFIER | c.271-4105A>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21020115 | |||||||
| chr9:21020117 | A | T | 1 | a0002c0002t0009g0169 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.271-4107T>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21020117 | |||||||
| chr9:21020128 | C | T | 242 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0002g0037 others(239): Show |
422 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(419): Show |
intron_variant | MODIFIER | c.271-4118G>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21020128 | |||||||
| chr9:21020169 | G | A | 32 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0005g0005 others(29): Show |
59 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(56): Show |
intron_variant | MODIFIER | c.271-4159C>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21020169 | |||||||
| chr9:21020175 | G | C | 2 | a0001c0001t0002g0108 a0001c0001t0002g0109 |
2 | HG01243.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.271-4165C>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21020175 | |||||||
| chr9:21020233 | GAC | G | 115 | a0001c0001t0002g0108 a0001c0001t0002g0109 a0001c0001t0002g0140 others(112): Show |
192 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(189): Show |
intron_variant | MODIFIER | c.271-4225_271-4224d others(4): Show |
HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21020233 | |||||||
| chr9:21020323 | G | A | 2 | a0002c0002t0008g0056 a0002c0002t0008g0184 |
3 | HG03041.hp2 HG03130.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.271-4313C>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21020323 | |||||||
| chr9:21020468 | AAC | A | 9 | a0001c0001t0012g0023 a0001c0001t0012g0152 a0001c0001t0012g0153 others(6): Show |
12 | HG02071.hp2 HG03669.hp2 NA18943.hp2 others(9): Show |
intron_variant | MODIFIER | c.271-4460_271-4459d others(4): Show |
HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21020468 | |||||||
| chr9:21020503 | C | G | 114 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0002g0037 others(111): Show |
209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.271-4493G>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21020503 | |||||||
| chr9:21020535 | T | A | 1 | a0002c0002t0009g0171 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.271-4525A>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21020535 | |||||||
| chr9:21020620 | G | A | 1 | a0002c0002t0001g0209 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.271-4610C>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21020620 | |||||||
| chr9:21020642 | A | G | 229 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0002g0037 others(226): Show |
401 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(398): Show |
intron_variant | MODIFIER | c.271-4632T>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21020642 | |||||||
| chr9:21020673 | T | C | 1 | a0001c0001t0028g0082 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.271-4663A>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21020673 | |||||||
| chr9:21020682 | T | A | 1 | a0002c0002t0001g0243 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.271-4672A>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21020682 | |||||||
| chr9:21020683 | C | G | 1 | a0002c0002t0001g0243 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.271-4673G>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21020683 | |||||||
| chr9:21020712 | G | A | 113 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0002g0037 others(110): Show |
207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.271-4702C>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21020712 | |||||||
| chr9:21020996 | C | T | 4 | a0001c0001t0002g0097 a0001c0001t0017g0062 a0001c0001t0017g0100 others(1): Show |
4 | HG02559.hp1 HG02717.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.271-4986G>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21020996 | |||||||
| chr9:21021247 | T | C | 114 | a0001c0001t0002g0140 a0001c0001t0006g0146 a0001c0001t0019g0022 others(111): Show |
192 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(189): Show |
intron_variant | MODIFIER | c.271-5237A>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21021247 | |||||||
| chr9:21021258 | C | T | 1 | a0002c0002t0001g0210 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.271-5248G>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21021258 | |||||||
| chr9:21021259 | G | C | 1 | a0002c0002t0001g0210 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.271-5249C>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21021259 | |||||||
| chr9:21021273 | T | C | 2 | a0001c0001t0002g0158 a0001c0001t0004g0093 |
2 | HG03516.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.271-5263A>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21021273 | |||||||
| chr9:21021281 | T | C | 113 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0002g0037 others(110): Show |
207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.271-5271A>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21021281 | |||||||
| chr9:21021386 | A | G | 114 | a0001c0001t0002g0140 a0001c0001t0006g0146 a0001c0001t0019g0022 others(111): Show |
192 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(189): Show |
intron_variant | MODIFIER | c.270+5210T>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21021386 | |||||||
| chr9:21021480 | C | G | 2 | a0001c0001t0006g0159 a0001c0001t0006g0160 |
2 | HG03209.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.270+5116G>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21021480 | |||||||
| chr9:21021492 | C | A | 1 | a0002c0002t0002g0179 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.270+5104G>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21021492 | |||||||
| chr9:21021552 | C | T | 1 | a0002c0002t0002g0143 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.270+5044G>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21021552 | |||||||
| chr9:21021553 | G | A | 1 | a0002c0002t0002g0143 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.270+5043C>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21021553 | |||||||
| chr9:21021559 | C | A | 1 | a0002c0002t0002g0143 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.270+5037G>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21021559 | |||||||
| chr9:21021575 | T | C | 68 | a0001c0001t0002g0037 a0001c0001t0002g0097 a0001c0001t0002g0117 others(65): Show |
132 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.270+5021A>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21021575 | |||||||
| chr9:21021669 | A | C | 2 | a0001c0001t0011g0094 a0001c0001t0055g0161 |
2 | HG02451.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.270+4927T>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21021669 | |||||||
| chr9:21021705 | A | G | 2 | a0001c0001t0002g0108 a0001c0001t0002g0109 |
2 | HG01243.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.270+4891T>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21021705 | |||||||
| chr9:21021783 | T | C | 113 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0002g0037 others(110): Show |
207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.270+4813A>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21021783 | |||||||
| chr9:21021903 | A | G | 1 | a0002c0002t0003g0185 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.270+4693T>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21021903 | |||||||
| chr9:21021914 | A | G | 1 | a0001c0001t0002g0097 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.270+4682T>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21021914 | |||||||
| chr9:21021943 | C | T | 1 | a0001c0001t0045g0069 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.270+4653G>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21021943 | |||||||
| chr9:21021953 | G | A | 106 | a0001c0001t0002g0140 a0002c0002t0001g0001 a0002c0002t0001g0017 others(103): Show |
181 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(178): Show |
intron_variant | MODIFIER | c.270+4643C>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21021953 | |||||||
| chr9:21021960 | C | G | 2 | a0001c0001t0002g0108 a0001c0001t0002g0109 |
2 | HG01243.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.270+4636G>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21021960 | |||||||
| chr9:21022000 | C | T | 2 | a0001c0001t0002g0108 a0001c0001t0002g0109 |
2 | HG01243.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.270+4596G>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21022000 | |||||||
| chr9:21022085 | A | G | 1 | a0001c0001t0006g0160 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.270+4511T>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21022085 | |||||||
| chr9:21022094 | A | G | 1 | a0001c0001t0005g0068 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.270+4502T>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21022094 | |||||||
| chr9:21022158 | A | G | 1 | a0001c0001t0006g0112 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.270+4438T>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21022158 | |||||||
| chr9:21022187 | A | G | 1 | a0001c0001t0004g0126 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.270+4409T>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21022187 | |||||||
| chr9:21022228 | C | T | 67 | a0001c0001t0002g0037 a0001c0001t0002g0097 a0001c0001t0002g0117 others(64): Show |
131 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(128): Show |
intron_variant | MODIFIER | c.270+4368G>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21022228 | |||||||
| chr9:21022359 | A | G | 33 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0005g0005 others(30): Show |
60 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(57): Show |
intron_variant | MODIFIER | c.270+4237T>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21022359 | |||||||
| chr9:21022402 | G | A | 1 | a0001c0001t0004g0103 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.270+4194C>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21022402 | |||||||
| chr9:21022501 | A | C | 114 | a0001c0001t0002g0140 a0001c0001t0006g0146 a0001c0001t0019g0022 others(111): Show |
192 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(189): Show |
intron_variant | MODIFIER | c.270+4095T>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21022501 | |||||||
| chr9:21022570 | A | G | 9 | a0001c0001t0012g0023 a0001c0001t0012g0152 a0001c0001t0012g0153 others(6): Show |
12 | HG02071.hp2 HG03669.hp2 NA18943.hp2 others(9): Show |
intron_variant | MODIFIER | c.270+4026T>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21022570 | |||||||
| chr9:21022597 | A | G | 14 | a0001c0001t0004g0009 a0001c0001t0004g0012 a0001c0001t0004g0019 others(11): Show |
38 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(35): Show |
intron_variant | MODIFIER | c.270+3999T>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21022597 | |||||||
| chr9:21022638 | T | TC | 228 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0002g0037 others(225): Show |
400 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(397): Show |
intron_variant | MODIFIER | c.270+3957_270+3958i others(3): Show |
HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21022638 | |||||||
| chr9:21022695 | A | G | 32 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0005g0005 others(29): Show |
58 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.270+3901T>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21022695 | |||||||
| chr9:21022815 | C | G | 5 | a0001c0001t0004g0106 a0001c0001t0018g0034 a0001c0001t0018g0104 others(2): Show |
6 | HG02572.hp2 HG02896.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.270+3781G>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21022815 | |||||||
| chr9:21022870 | A | C | 114 | a0001c0001t0002g0140 a0001c0001t0006g0146 a0001c0001t0019g0022 others(111): Show |
192 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(189): Show |
intron_variant | MODIFIER | c.270+3726T>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21022870 | |||||||
| chr9:21022901 | A | G | 8 | a0001c0001t0004g0009 a0001c0001t0004g0126 a0001c0001t0004g0129 others(5): Show |
24 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(21): Show |
intron_variant | MODIFIER | c.270+3695T>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21022901 | |||||||
| chr9:21022905 | A | C | 113 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0002g0037 others(110): Show |
208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.270+3691T>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21022905 | |||||||
| chr9:21023022 | C | T | 3 | a0001c0001t0011g0094 a0001c0001t0055g0161 a0002c0002t0008g0184 |
3 | HG02451.hp1 HG03041.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.270+3574G>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21023022 | |||||||
| chr9:21023052 | G | C | 2 | a0001c0001t0002g0037 a0001c0001t0003g0014 |
6 | HG00544.hp1 HG01993.hp1 HG02040.hp2 others(3): Show |
intron_variant | MODIFIER | c.270+3544C>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21023052 | |||||||
| chr9:21023090 | C | G | 1 | a0002c0002t0001g0183 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.270+3506G>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21023090 | |||||||
| chr9:21023196 | T | C | 2 | a0002c0002t0002g0211 a0002c0002t0002g0212 |
2 | NA18983.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.270+3400A>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21023196 | |||||||
| chr9:21023265 | A | C | 1 | a0002c0002t0004g0182 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.270+3331T>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21023265 | |||||||
| chr9:21023305 | C | G | 33 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0005g0005 others(30): Show |
60 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(57): Show |
intron_variant | MODIFIER | c.270+3291G>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21023305 | |||||||
| chr9:21023447 | C | T | 114 | a0001c0001t0002g0140 a0001c0001t0006g0146 a0001c0001t0019g0022 others(111): Show |
192 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(189): Show |
intron_variant | MODIFIER | c.270+3149G>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21023447 | |||||||
| chr9:21023574 | C | CT | 111 | a0001c0001t0002g0140 a0001c0001t0003g0035 a0001c0001t0003g0114 others(108): Show |
191 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(188): Show |
intron_variant | MODIFIER | c.270+3021dupA | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21023574 | |||||||
| chr9:21023612 | T | C | 1 | a0002c0002t0001g0217 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.270+2984A>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21023612 | |||||||
| chr9:21023715 | C | T | 1 | a0001c0001t0027g0067 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.270+2881G>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21023715 | |||||||
| chr9:21023737 | G | C | 2 | a0001c0001t0006g0112 a0001c0001t0006g0113 |
2 | HG01070.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.270+2859C>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21023737 | |||||||
| chr9:21023827 | A | G | 228 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0002g0037 others(225): Show |
400 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(397): Show |
intron_variant | MODIFIER | c.270+2769T>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21023827 | |||||||
| chr9:21023926 | G | C | 2 | a0002c0002t0001g0180 a0002c0002t0001g0181 |
2 | HG03017.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.270+2670C>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21023926 | |||||||
| chr9:21023939 | A | G | 114 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0002g0037 others(111): Show |
209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.270+2657T>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21023939 | |||||||
| chr9:21024004 | A | G | 1 | a0001c0001t0011g0094 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.270+2592T>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21024004 | |||||||
| chr9:21024021 | C | T | 1 | a0002c0002t0023g0227 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.270+2575G>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21024021 | |||||||
| chr9:21024065 | C | T | 1 | a0001c0001t0003g0021 | 3 | NA18957.hp2 NA18959.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.270+2531G>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21024065 | |||||||
| chr9:21024104 | T | C | 226 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0002g0037 others(223): Show |
398 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(395): Show |
intron_variant | MODIFIER | c.270+2492A>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21024104 | |||||||
| chr9:21024119 | G | A | 2 | a0002c0002t0001g0218 a0002c0002t0001g0241 |
2 | NA18950.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.270+2477C>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21024119 | |||||||
| chr9:21024223 | A | T | 2 | a0002c0002t0001g0180 a0002c0002t0001g0181 |
2 | HG03017.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.270+2373T>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21024223 | |||||||
| chr9:21024236 | T | C | 1 | a0002c0002t0001g0219 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.270+2360A>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21024236 | |||||||
| chr9:21024289 | A | G | 2 | a0001c0001t0006g0112 a0001c0001t0006g0113 |
2 | HG01070.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.270+2307T>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21024289 | |||||||
| chr9:21024295 | T | C | 226 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0002g0037 others(223): Show |
398 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(395): Show |
intron_variant | MODIFIER | c.270+2301A>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21024295 | |||||||
| chr9:21024385 | C | G | 2 | a0001c0001t0002g0108 a0001c0001t0002g0109 |
2 | HG01243.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.270+2211G>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21024385 | |||||||
| chr9:21024582 | G | T | 2 | a0002c0002t0002g0178 a0002c0002t0002g0179 |
2 | HG00280.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.270+2014C>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21024582 | |||||||
| chr9:21024671 | G | A | 113 | a0001c0001t0002g0140 a0001c0001t0019g0022 a0002c0002t0001g0001 others(110): Show |
191 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(188): Show |
intron_variant | MODIFIER | c.270+1925C>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21024671 | |||||||
| chr9:21024724 | C | A | 37 | a0001c0001t0002g0097 a0001c0001t0002g0158 a0001c0001t0004g0009 others(34): Show |
66 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(63): Show |
intron_variant | MODIFIER | c.270+1872G>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21024724 | |||||||
| chr9:21024798 | A | C | 1 | a0001c0001t0019g0022 | 3 | HG01074.hp2 HG02451.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.270+1798T>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21024798 | |||||||
| chr9:21024852 | G | A | 104 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0002g0037 others(101): Show |
195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.270+1744C>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21024852 | |||||||
| chr9:21024872 | C | A | 1 | a0002c0002t0001g0044 | 2 | HG03704.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.270+1724G>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21024872 | |||||||
| chr9:21024881 | T | A | 1 | a0001c0001t0005g0083 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.270+1715A>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21024881 | |||||||
| chr9:21024903 | T | C | 9 | a0001c0001t0012g0023 a0001c0001t0012g0152 a0001c0001t0012g0153 others(6): Show |
12 | HG02071.hp2 HG03669.hp2 NA18943.hp2 others(9): Show |
intron_variant | MODIFIER | c.270+1693A>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21024903 | |||||||
| chr9:21024942 | A | G | 225 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0002g0037 others(222): Show |
397 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(394): Show |
intron_variant | MODIFIER | c.270+1654T>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21024942 | |||||||
| chr9:21025157 | A | G | 2 | a0001c0001t0004g0033 a0001c0001t0004g0098 |
3 | HG02630.hp2 HG02647.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.270+1439T>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21025157 | |||||||
| chr9:21025178 | T | C | 227 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0002g0037 others(224): Show |
399 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(396): Show |
intron_variant | MODIFIER | c.270+1418A>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21025178 | |||||||
| chr9:21025334 | A | G | 1 | a0001c0001t0003g0107 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.270+1262T>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21025334 | |||||||
| chr9:21025409 | A | ACATT | 111 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0002g0037 others(108): Show |
205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.270+1183_270+1186d others(6): Show |
HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21025409 | |||||||
| chr9:21025703 | C | G | 1 | a0001c0001t0005g0066 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.270+893G>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21025703 | |||||||
| chr9:21026317 | T | C | 114 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0002g0037 others(111): Show |
209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.270+279A>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21026317 | |||||||
| chr9:21026362 | T | G | 1 | a0002c0002t0002g0220 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.270+234A>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21026362 | |||||||
| chr9:21026407 | A | C | 1 | a0001c0001t0052g0105 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.270+189T>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21026407 | |||||||
| chr9:21026541 | G | T | 114 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0002g0037 others(111): Show |
209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.270+55C>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 3/6 | chr9 | 21026541 | |||||||
| chr9:21026801 | G | A | 113 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0002g0037 others(110): Show |
207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.143-78C>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 2/6 | chr9 | 21026801 | |||||||
| chr9:21026881 | C | A | 1 | a0001c0001t0012g0154 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.143-158G>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 2/6 | chr9 | 21026881 | |||||||
| chr9:21026894 | C | G | 228 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0002g0037 others(225): Show |
400 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(397): Show |
intron_variant | MODIFIER | c.143-171G>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 2/6 | chr9 | 21026894 | |||||||
| chr9:21026948 | G | A | 1 | a0002c0002t0001g0221 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.143-225C>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 2/6 | chr9 | 21026948 | |||||||
| chr9:21026982 | C | G | 2 | a0001c0001t0020g0030 a0001c0001t0020g0085 |
3 | HG02486.hp2 HG03195.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.143-259G>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 2/6 | chr9 | 21026982 | |||||||
| chr9:21027003 | A | G | 113 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0002g0037 others(110): Show |
207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.143-280T>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 2/6 | chr9 | 21027003 | |||||||
| chr9:21027208 | T | C | 2 | a0001c0001t0012g0153 a0001c0001t0012g0154 |
2 | NA19081.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.143-485A>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 2/6 | chr9 | 21027208 | |||||||
| chr9:21027265 | C | T | 113 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0002g0037 others(110): Show |
207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.143-542G>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 2/6 | chr9 | 21027265 | |||||||
| chr9:21027299 | G | C | 4 | a0001c0001t0002g0095 a0001c0001t0003g0107 a0001c0001t0011g0094 others(1): Show |
4 | HG01123.hp1 HG02451.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.143-576C>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 2/6 | chr9 | 21027299 | |||||||
| chr9:21027321 | C | A | 114 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0002g0037 others(111): Show |
208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.143-598G>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 2/6 | chr9 | 21027321 | |||||||
| chr9:21027366 | G | C | 2 | a0001c0001t0014g0008 a0001c0001t0014g0110 |
8 | HG00639.hp1 HG00642.hp1 HG01069.hp1 others(5): Show |
intron_variant | MODIFIER | c.143-643C>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 2/6 | chr9 | 21027366 | |||||||
| chr9:21027434 | G | A | 1 | a0001c0001t0003g0141 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.143-711C>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 2/6 | chr9 | 21027434 | |||||||
| chr9:21027516 | G | A | 4 | a0001c0001t0003g0013 a0001c0001t0003g0047 a0001c0001t0003g0174 others(1): Show |
9 | NA18964.hp2 NA18973.hp1 NA18979.hp1 others(6): Show |
intron_variant | MODIFIER | c.143-793C>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 2/6 | chr9 | 21027516 | |||||||
| chr9:21027520 | G | C | 4 | a0001c0001t0002g0095 a0001c0001t0003g0107 a0001c0001t0011g0094 others(1): Show |
4 | HG01123.hp1 HG02451.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.143-797C>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 2/6 | chr9 | 21027520 | |||||||
| chr9:21027742 | A | G | 113 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0002g0037 others(110): Show |
207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.143-1019T>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 2/6 | chr9 | 21027742 | |||||||
| chr9:21027772 | T | G | 2 | a0002c0002t0001g0057 a0005c0007t0001g0223 |
3 | HG02129.hp1 HG02155.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.143-1049A>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 2/6 | chr9 | 21027772 | |||||||
| chr9:21027790 | T | C | 1 | a0002c0002t0002g0224 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.143-1067A>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 2/6 | chr9 | 21027790 | |||||||
| chr9:21027801 | T | A | 1 | a0002c0002t0001g0225 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.143-1078A>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 2/6 | chr9 | 21027801 | |||||||
| chr9:21027816 | G | T | 75 | a0001c0001t0002g0037 a0001c0001t0002g0097 a0001c0001t0002g0117 others(72): Show |
142 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.143-1093C>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 2/6 | chr9 | 21027816 | |||||||
| chr9:21027856 | C | T | 2 | a0001c0001t0002g0095 a0001c0001t0011g0094 |
2 | HG01123.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.143-1133G>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 2/6 | chr9 | 21027856 | |||||||
| chr9:21027909 | C | T | 2 | a0001c0001t0002g0108 a0001c0001t0002g0109 |
2 | HG01243.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.143-1186G>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 2/6 | chr9 | 21027909 | |||||||
| chr9:21028003 | C | T | 1 | a0001c0001t0002g0095 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.143-1280G>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 2/6 | chr9 | 21028003 | |||||||
| chr9:21028072 | T | A | 3 | a0002c0002t0001g0018 a0002c0002t0001g0242 a0002c0002t0043g0226 |
6 | HG01346.hp2 HG01928.hp2 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.142+1223A>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 2/6 | chr9 | 21028072 | |||||||
| chr9:21028119 | G | A | 1 | a0001c0001t0019g0022 | 3 | HG01074.hp2 HG02451.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.142+1176C>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 2/6 | chr9 | 21028119 | |||||||
| chr9:21028135 | C | CA | 139 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0002g0095 others(136): Show |
241 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.142+1159dupT | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 2/6 | chr9 | 21028135 | |||||||
| chr9:21028135 | C | CAA | 8 | a0001c0001t0005g0084 a0001c0001t0020g0085 a0002c0002t0001g0230 others(5): Show |
9 | HG02615.hp1 HG02615.hp2 HG02976.hp2 others(6): Show |
intron_variant | MODIFIER | c.142+1158_142+1159d others(4): Show |
HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 2/6 | chr9 | 21028135 | |||||||
| chr9:21028162 | A | G | 1 | a0002c0002t0001g0001 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.142+1133T>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 2/6 | chr9 | 21028162 | |||||||
| chr9:21028169 | A | G | 1 | a0002c0002t0001g0048 | 2 | HG02074.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.142+1126T>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 2/6 | chr9 | 21028169 | |||||||
| chr9:21028333 | A | C | 2 | a0001c0001t0006g0159 a0001c0001t0006g0160 |
2 | HG03209.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.142+962T>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 2/6 | chr9 | 21028333 | |||||||
| chr9:21028362 | T | G | 1 | a0002c0002t0008g0231 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.142+933A>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 2/6 | chr9 | 21028362 | |||||||
| chr9:21028471 | G | A | 1 | a0001c0001t0055g0161 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.142+824C>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 2/6 | chr9 | 21028471 | |||||||
| chr9:21028536 | C | G | 76 | a0001c0001t0002g0037 a0001c0001t0002g0097 a0001c0001t0002g0117 others(73): Show |
143 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.142+759G>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 2/6 | chr9 | 21028536 | |||||||
| chr9:21028541 | C | T | 7 | a0001c0001t0012g0023 a0001c0001t0012g0152 a0001c0001t0012g0153 others(4): Show |
9 | HG03669.hp2 NA18945.hp2 NA18960.hp2 others(6): Show |
intron_variant | MODIFIER | c.142+754G>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 2/6 | chr9 | 21028541 | |||||||
| chr9:21028637 | C | T | 112 | a0002c0002t0001g0001 a0002c0002t0001g0017 a0002c0002t0001g0018 others(109): Show |
188 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(185): Show |
intron_variant | MODIFIER | c.142+658G>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 2/6 | chr9 | 21028637 | |||||||
| chr9:21028670 | C | T | 1 | a0001c0001t0002g0097 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.142+625G>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 2/6 | chr9 | 21028670 | |||||||
| chr9:21028782 | C | CTA | 3 | a0001c0001t0002g0108 a0001c0001t0002g0109 a0001c0001t0019g0022 |
5 | HG01074.hp2 HG01243.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.142+511_142+512dup others(2): Show |
HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 2/6 | chr9 | 21028782 | |||||||
| chr9:21028851 | G | T | 2 | a0001c0001t0002g0095 a0001c0001t0011g0094 |
2 | HG01123.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.142+444C>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 2/6 | chr9 | 21028851 | |||||||
| chr9:21029067 | C | G | 1 | a0002c0002t0026g0176 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.142+228G>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 2/6 | chr9 | 21029067 | |||||||
| chr9:21029239 | T | A | 1 | a0001c0001t0055g0161 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.142+56A>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 2/6 | chr9 | 21029239 | |||||||
| chr9:21029494 | G | A | 3 | a0001c0001t0018g0034 a0001c0001t0018g0104 a0001c0001t0052g0105 |
4 | HG02572.hp2 HG02970.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.39-96C>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 1/6 | chr9 | 21029494 | |||||||
| chr9:21029626 | G | C | 1 | a0001c0001t0055g0161 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.39-228C>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 1/6 | chr9 | 21029626 | |||||||
| chr9:21029688 | A | G | 1 | a0002c0002t0001g0168 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.39-290T>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 1/6 | chr9 | 21029688 | |||||||
| chr9:21029707 | C | T | 4 | a0001c0001t0002g0095 a0001c0001t0003g0107 a0001c0001t0011g0094 others(1): Show |
4 | HG01123.hp1 HG02451.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.39-309G>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 1/6 | chr9 | 21029707 | |||||||
| chr9:21029803 | G | C | 69 | a0001c0001t0002g0037 a0001c0001t0002g0097 a0001c0001t0002g0117 others(66): Show |
130 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.39-405C>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 1/6 | chr9 | 21029803 | |||||||
| chr9:21029834 | T | C | 1 | a0002c0002t0001g0232 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.39-436A>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 1/6 | chr9 | 21029834 | |||||||
| chr9:21029841 | G | A | 4 | a0001c0001t0002g0095 a0001c0001t0003g0107 a0001c0001t0011g0094 others(1): Show |
4 | HG01123.hp1 HG02451.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.39-443C>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 1/6 | chr9 | 21029841 | |||||||
| chr9:21029864 | C | T | 227 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0002g0037 others(224): Show |
399 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(396): Show |
intron_variant | MODIFIER | c.39-466G>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 1/6 | chr9 | 21029864 | |||||||
| chr9:21029877 | C | T | 62 | a0001c0001t0002g0037 a0001c0001t0002g0097 a0001c0001t0002g0117 others(59): Show |
121 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.39-479G>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 1/6 | chr9 | 21029877 | |||||||
| chr9:21029963 | T | A | 2 | a0002c0002t0022g0233 a0002c0002t0022g0234 |
2 | HG02135.hp2 NA18942.hp1 |
intron_variant | MODIFIER | c.39-565A>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 1/6 | chr9 | 21029963 | |||||||
| chr9:21030093 | G | T | 6 | a0002c0002t0001g0168 a0002c0002t0009g0006 a0002c0002t0009g0164 others(3): Show |
15 | NA18944.hp2 NA18945.hp1 NA18955.hp2 others(12): Show |
intron_variant | MODIFIER | c.39-695C>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 1/6 | chr9 | 21030093 | |||||||
| chr9:21030094 | C | T | 6 | a0002c0002t0001g0168 a0002c0002t0009g0006 a0002c0002t0009g0164 others(3): Show |
15 | NA18944.hp2 NA18945.hp1 NA18955.hp2 others(12): Show |
intron_variant | MODIFIER | c.39-696G>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 1/6 | chr9 | 21030094 | |||||||
| chr9:21030166 | C | T | 102 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0002g0037 others(99): Show |
190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.39-768G>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 1/6 | chr9 | 21030166 | |||||||
| chr9:21030182 | T | C | 1 | a0001c0001t0055g0161 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.39-784A>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 1/6 | chr9 | 21030182 | |||||||
| chr9:21030269 | C | CA | 111 | a0001c0001t0002g0108 a0001c0001t0002g0109 a0001c0001t0003g0013 others(108): Show |
195 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(192): Show |
intron_variant | MODIFIER | c.39-872dupT | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 1/6 | chr9 | 21030269 | |||||||
| chr9:21030269 | C | CAA | 14 | a0001c0001t0002g0095 a0001c0001t0003g0107 a0001c0001t0003g0235 others(11): Show |
16 | HG00642.hp2 HG01123.hp1 HG01975.hp2 others(13): Show |
intron_variant | MODIFIER | c.39-873_39-872dupTT | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 1/6 | chr9 | 21030269 | |||||||
| chr9:21030269 | CA | C | 49 | a0001c0001t0002g0037 a0001c0001t0002g0097 a0001c0001t0002g0117 others(46): Show |
103 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.39-872delT | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 1/6 | chr9 | 21030269 | |||||||
| chr9:21030284 | A | C | 1 | a0002c0002t0002g0163 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.39-886T>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 1/6 | chr9 | 21030284 | |||||||
| chr9:21030387 | A | T | 2 | a0001c0001t0006g0146 a0001c0001t0019g0022 |
4 | HG01074.hp2 HG02451.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.39-989T>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 1/6 | chr9 | 21030387 | |||||||
| chr9:21030483 | C | A | 1 | a0002c0002t0001g0243 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.38+1070G>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 1/6 | chr9 | 21030483 | |||||||
| chr9:21030691 | C | A | 70 | a0001c0001t0002g0037 a0001c0001t0002g0097 a0001c0001t0002g0117 others(67): Show |
132 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.38+862G>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 1/6 | chr9 | 21030691 | |||||||
| chr9:21030733 | T | C | 2 | a0002c0002t0011g0244 a0002c0002t0050g0245 |
2 | HG03195.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.38+820A>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 1/6 | chr9 | 21030733 | |||||||
| chr9:21030769 | G | A | 2 | a0001c0001t0006g0146 a0001c0001t0019g0022 |
4 | HG01074.hp2 HG02451.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.38+784C>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 1/6 | chr9 | 21030769 | |||||||
| chr9:21030821 | C | G | 1 | a0006c0008t0002g0162 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.38+732G>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 1/6 | chr9 | 21030821 | |||||||
| chr9:21030824 | A | G | 2 | a0001c0001t0006g0146 a0001c0001t0019g0022 |
4 | HG01074.hp2 HG02451.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.38+729T>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 1/6 | chr9 | 21030824 | |||||||
| chr9:21030852 | G | A | 119 | a0001c0001t0002g0108 a0001c0001t0002g0109 a0001c0001t0003g0013 others(116): Show |
200 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(197): Show |
intron_variant | MODIFIER | c.38+701C>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 1/6 | chr9 | 21030852 | |||||||
| chr9:21030908 | G | C | 70 | a0001c0001t0002g0037 a0001c0001t0002g0097 a0001c0001t0002g0117 others(67): Show |
132 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.38+645C>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 1/6 | chr9 | 21030908 | |||||||
| chr9:21030936 | T | G | 1 | a0001c0001t0012g0156 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.38+617A>C | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 1/6 | chr9 | 21030936 | |||||||
| chr9:21030996 | T | A | 2 | a0002c0002t0002g0144 a0002c0002t0002g0145 |
2 | NA18952.hp2 NA18956.hp1 |
intron_variant | MODIFIER | c.38+557A>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 1/6 | chr9 | 21030996 | |||||||
| chr9:21031116 | C | T | 28 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0005g0005 others(25): Show |
54 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(51): Show |
intron_variant | MODIFIER | c.38+437G>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 1/6 | chr9 | 21031116 | |||||||
| chr9:21031153 | C | A | 121 | a0001c0001t0002g0108 a0001c0001t0002g0109 a0001c0001t0003g0013 others(118): Show |
205 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.38+400G>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 1/6 | chr9 | 21031153 | |||||||
| chr9:21031154 | G | C | 187 | a0001c0001t0002g0037 a0001c0001t0002g0095 a0001c0001t0002g0097 others(184): Show |
328 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(325): Show |
intron_variant | MODIFIER | c.38+399C>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 1/6 | chr9 | 21031154 | |||||||
| chr9:21031264 | G | C | 1 | a0002c0002t0002g0061 | 2 | NA19009.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.38+289C>G | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 1/6 | chr9 | 21031264 | |||||||
| chr9:21031353 | C | A | 2 | a0001c0001t0014g0008 a0001c0001t0014g0110 |
8 | HG00639.hp1 HG00642.hp1 HG01069.hp1 others(5): Show |
intron_variant | MODIFIER | c.38+200G>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 1/6 | chr9 | 21031353 | |||||||
| chr9:21031455 | C | T | 1 | a0001c0001t0017g0062 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.38+98G>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 1/6 | chr9 | 21031455 | |||||||
| chr9:21031472 | C | A | 52 | a0001c0001t0002g0037 a0001c0001t0002g0117 a0001c0001t0002g0123 others(49): Show |
105 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.38+81G>T | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 1/6 | chr9 | 21031472 | |||||||
| chr9:21031480 | C | T | 113 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0002g0037 others(110): Show |
203 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(200): Show |
intron_variant | MODIFIER | c.38+73G>A | HACD4 | ENSG00000188921.14 | transcript | ENST00000495827.3 | protein_coding | 1/6 | chr9 | 21031480 |