Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 51191 |
| ensemblid | ENSG00000138646.9 |
| hgncid | 24368 |
| symbol | HERC5 |
| name | HECT and RLD domain containing E3 ubiquitin protein ligase 5 |
| refseq_nuc | NM_016323.4 |
| refseq_prot | NP_057407.2 |
| ensembl_nuc | ENST00000264350.8 |
| ensembl_prot | ENSP00000264350.3 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 88457119 |
| end | 88506163 |
| strand | + |
| ver | v1.2 |
| region | chr4:88457119-88506163 |
| region5000 | chr4:88452119-88511163 |
| regionname0 | HERC5_chr4_88457119_88506163 |
| regionname5000 | HERC5_chr4_88452119_88511163 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 1024 | 211 | 69 | 34 | 87 | 5 | 15 | 64 | HERC5_chr4_88452119_88511163 | HERC5 | MERRS others(1019): Show |
chr4 | 88452119 | 88511163 |
| a0002 | 1/0 | 1024 | 96 | 13 | 21 | 43 | 5 | 13 | 32 | HERC5_chr4_88452119_88511163 | HERC5 | MERRS others(1019): Show |
chr4 | 88452119 | 88511163 |
| a0003 | 0/0 | 1024 | 13 | 0 | 6 | 7 | 0 | 0 | 6 | HERC5_chr4_88452119_88511163 | HERC5 | MERRS others(1019): Show |
chr4 | 88452119 | 88511163 |
| a0004 | 0/0 | 1024 | 6 | 5 | 1 | 0 | 0 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | MERRS others(1019): Show |
chr4 | 88452119 | 88511163 |
| a0005 | 0/0 | 1024 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | MERRS others(1019): Show |
chr4 | 88452119 | 88511163 |
| a0006 | 0/0 | 1024 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | MERRS others(1019): Show |
chr4 | 88452119 | 88511163 |
| a0007 | 0/0 | 1024 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HERC5_chr4_88452119_88511163 | HERC5 | MERRS others(1019): Show |
chr4 | 88452119 | 88511163 |
| a0008 | 0/0 | 1024 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HERC5_chr4_88452119_88511163 | HERC5 | MERRS others(1019): Show |
chr4 | 88452119 | 88511163 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 3072 | 195 | 63 | 31 | 86 | 2 | 13 | HERC5_chr4_88452119_88511163 | HERC5 | ATGGA others(3067): Show |
chr4 | 88452119 | 88511163 | ||
| a0001c0004 | 0/0 | 3072 | 8 | 0 | 3 | 0 | 3 | 2 | HERC5_chr4_88452119_88511163 | HERC5 | ATGGA others(3067): Show |
chr4 | 88452119 | 88511163 | ||
| a0001c0006 | 0/0 | 3072 | 5 | 5 | 0 | 0 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | ATGGA others(3067): Show |
chr4 | 88452119 | 88511163 | ||
| a0001c0008 | 0/0 | 3072 | 1 | 1 | 0 | 0 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | ATGGA others(3067): Show |
chr4 | 88452119 | 88511163 | ||
| a0001c0012 | 0/1 | 3072 | 1 | 0 | 0 | 0 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | ATGGA others(3067): Show |
chr4 | 88452119 | 88511163 | ||
| a0001c0014 | 0/0 | 3072 | 1 | 0 | 0 | 1 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | ATGGA others(3067): Show |
chr4 | 88452119 | 88511163 | ||
| a0002c0002 | 1/0 | 3072 | 95 | 12 | 21 | 43 | 5 | 13 | HERC5_chr4_88452119_88511163 | HERC5 | ATGGA others(3067): Show |
chr4 | 88452119 | 88511163 | ||
| a0002c0010 | 0/0 | 3072 | 1 | 1 | 0 | 0 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | ATGGA others(3067): Show |
chr4 | 88452119 | 88511163 | ||
| a0003c0003 | 0/0 | 3072 | 13 | 0 | 6 | 7 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | ATGGA others(3067): Show |
chr4 | 88452119 | 88511163 | ||
| a0004c0005 | 0/0 | 3072 | 6 | 5 | 1 | 0 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | ATGGA others(3067): Show |
chr4 | 88452119 | 88511163 | ||
| a0005c0013 | 0/0 | 3072 | 1 | 0 | 0 | 1 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | ATGGA others(3067): Show |
chr4 | 88452119 | 88511163 | ||
| a0006c0011 | 0/0 | 3072 | 1 | 1 | 0 | 0 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | ATGGA others(3067): Show |
chr4 | 88452119 | 88511163 | ||
| a0007c0007 | 0/0 | 3072 | 1 | 0 | 0 | 1 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | ATGGA others(3067): Show |
chr4 | 88452119 | 88511163 | ||
| a0008c0009 | 0/0 | 3072 | 1 | 0 | 0 | 1 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | ATGGA others(3067): Show |
chr4 | 88452119 | 88511163 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3511 | 182 | 55 | 30 | 86 | 2 | 9 | HERC5_chr4_88452119_88511163 | HERC5 | AGTAG others(3506): Show |
chr4 | 88452119 | 88511163 |
| a0001c0001t0002 | 0/0 | 3511 | 7 | 6 | 1 | 0 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | AGTAG others(3506): Show |
chr4 | 88452119 | 88511163 |
| a0001c0001t0003 | 0/0 | 3514 | 3 | 2 | 0 | 0 | 0 | 1 | HERC5_chr4_88452119_88511163 | HERC5 | AGTAG others(3509): Show |
chr4 | 88452119 | 88511163 |
| a0001c0001t0004 | 0/0 | 3511 | 3 | 0 | 0 | 0 | 0 | 3 | HERC5_chr4_88452119_88511163 | HERC5 | AGTAG others(3506): Show |
chr4 | 88452119 | 88511163 |
| a0001c0004t0001 | 0/0 | 3511 | 8 | 0 | 3 | 0 | 3 | 2 | HERC5_chr4_88452119_88511163 | HERC5 | AGTAG others(3506): Show |
chr4 | 88452119 | 88511163 |
| a0001c0006t0001 | 0/0 | 3511 | 5 | 5 | 0 | 0 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | AGTAG others(3506): Show |
chr4 | 88452119 | 88511163 |
| a0001c0008t0002 | 0/0 | 3511 | 1 | 1 | 0 | 0 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | AGTAG others(3506): Show |
chr4 | 88452119 | 88511163 |
| a0001c0012t0001 | 0/1 | 3511 | 1 | 0 | 0 | 0 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | AGTAG others(3506): Show |
chr4 | 88452119 | 88511163 |
| a0001c0014t0001 | 0/0 | 3511 | 1 | 0 | 0 | 1 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | AGTAG others(3506): Show |
chr4 | 88452119 | 88511163 |
| a0002c0002t0001 | 1/0 | 3511 | 90 | 12 | 18 | 43 | 4 | 12 | HERC5_chr4_88452119_88511163 | HERC5 | AGTAG others(3506): Show |
chr4 | 88452119 | 88511163 |
| a0002c0002t0005 | 0/0 | 3508 | 3 | 0 | 2 | 0 | 1 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | AGTAG others(3503): Show |
chr4 | 88452119 | 88511163 |
| a0002c0002t0006 | 0/0 | 3511 | 1 | 0 | 1 | 0 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | AGTAG others(3506): Show |
chr4 | 88452119 | 88511163 |
| a0002c0002t0007 | 0/0 | 3511 | 1 | 0 | 0 | 0 | 0 | 1 | HERC5_chr4_88452119_88511163 | HERC5 | AGTAG others(3506): Show |
chr4 | 88452119 | 88511163 |
| a0002c0010t0001 | 0/0 | 3511 | 1 | 1 | 0 | 0 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | AGTAG others(3506): Show |
chr4 | 88452119 | 88511163 |
| a0003c0003t0001 | 0/0 | 3511 | 13 | 0 | 6 | 7 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | AGTAG others(3506): Show |
chr4 | 88452119 | 88511163 |
| a0004c0005t0001 | 0/0 | 3511 | 6 | 5 | 1 | 0 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | AGTAG others(3506): Show |
chr4 | 88452119 | 88511163 |
| a0005c0013t0001 | 0/0 | 3511 | 1 | 0 | 0 | 1 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | AGTAG others(3506): Show |
chr4 | 88452119 | 88511163 |
| a0006c0011t0001 | 0/0 | 3511 | 1 | 1 | 0 | 0 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | AGTAG others(3506): Show |
chr4 | 88452119 | 88511163 |
| a0007c0007t0001 | 0/0 | 3511 | 1 | 0 | 0 | 1 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | AGTAG others(3506): Show |
chr4 | 88452119 | 88511163 |
| a0008c0009t0001 | 0/0 | 3511 | 1 | 0 | 0 | 1 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | AGTAG others(3506): Show |
chr4 | 88452119 | 88511163 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0002 | 0/0 | 8 | 0 | 6 | 2 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0004 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0008 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0009 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0010 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0011 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0002g0014 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0002g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0002g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0002g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0002g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0003g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0003g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0003g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0004g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0004g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0001t0004g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0004t0001g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0004t0001g0017 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0004t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0004t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0004t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0004t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0004t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0006t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0006t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0006t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0006t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0008t0002g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0012t0001g0002 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0001c0014t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0002c0002t0001g0003 | 1/0 | 6 | 1 | 2 | 1 | 1 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0002c0002t0001g0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0002c0002t0001g0012 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0002c0002t0001g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0002c0002t0001g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0002c0002t0001g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0002c0002t0001g0022 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0002c0002t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0002c0002t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0002c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0002c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0002c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0002c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0002c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0002c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0002c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0002c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0002c0002t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0002c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0002c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0002c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0002c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0002c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0002c0002t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0002c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0002c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0002c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0002c0002t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0002c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0002c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0002c0002t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0002c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0002c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0002c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0002c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0002c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0002c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0002c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0002c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0002c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0002c0002t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0002c0002t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0002c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0002c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0002c0002t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0002c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0002c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0002c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0002c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0002c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0002c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0002c0002t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0002c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0002c0002t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0002c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0002c0002t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0002c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0002c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0002c0002t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0002c0002t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0002c0002t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0002c0002t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0002c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0002c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0002c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0002c0002t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0002c0002t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0002c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0002c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0002c0002t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0002c0002t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0002c0002t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0002c0002t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0002c0002t0005g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0002c0002t0005g0016 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0002c0002t0005g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0002c0002t0006g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0002c0002t0007g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0002c0010t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0003c0003t0001g0001 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0003c0003t0001g0007 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0003c0003t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0003c0003t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0003c0003t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0004c0005t0001g0003 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0004c0005t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0004c0005t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0004c0005t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0004c0005t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0005c0013t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0006c0011t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0007c0007t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| a0008c0009t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0002 | c0002 | t0005 | g0016 | EUR | GBR | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG00140 | hp2 | a0001 | c0004 | t0001 | g0017 | EUR | GBR | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG00280 | hp1 | a0001 | c0004 | t0001 | g0054 | EUR | FIN | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG00280 | hp2 | a0002 | c0002 | t0001 | g0177 | EUR | FIN | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG00323 | hp1 | a0001 | c0004 | t0001 | g0017 | EUR | FIN | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG00323 | hp2 | a0002 | c0002 | t0001 | g0003 | EUR | FIN | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | CHS | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG00408 | hp2 | a0002 | c0002 | t0001 | g0183 | EAS | CHS | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG00423 | hp1 | a0002 | c0002 | t0001 | g0104 | EAS | CHS | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG00423 | hp2 | a0002 | c0002 | t0001 | g0205 | EAS | CHS | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG00438 | hp1 | a0005 | c0013 | t0001 | g0047 | EAS | CHS | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | CHS | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG00544 | hp1 | a0002 | c0002 | t0001 | g0203 | EAS | CHS | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | CHS | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | CHS | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG00597 | hp1 | a0002 | c0002 | t0001 | g0244 | EAS | CHS | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | CHS | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | CHS | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | CHS | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG00639 | hp1 | a0001 | c0004 | t0001 | g0038 | AMR | PUR | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG00639 | hp2 | a0002 | c0002 | t0001 | g0012 | AMR | PUR | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG00642 | hp1 | a0002 | c0002 | t0001 | g0232 | AMR | PUR | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0101 | AMR | PUR | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0053 | AMR | PUR | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG00735 | hp2 | a0002 | c0002 | t0001 | g0003 | AMR | PUR | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG00738 | hp1 | a0002 | c0002 | t0001 | g0031 | AMR | PUR | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG00738 | hp2 | a0002 | c0002 | t0005 | g0003 | AMR | PUR | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG00741 | hp1 | a0002 | c0002 | t0001 | g0181 | AMR | PUR | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG01069 | hp2 | a0002 | c0002 | t0005 | g0176 | AMR | PUR | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0157 | AMR | PUR | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG01099 | hp1 | a0002 | c0002 | t0001 | g0219 | AMR | PUR | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG01099 | hp2 | a0002 | c0002 | t0006 | g0223 | AMR | PUR | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG01106 | hp1 | a0002 | c0002 | t0001 | g0222 | AMR | PUR | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | PUR | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG01109 | hp1 | a0003 | c0003 | t0001 | g0007 | AMR | PUR | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG01109 | hp2 | a0002 | c0002 | t0001 | g0012 | AMR | PUR | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG01168 | hp2 | a0002 | c0002 | t0001 | g0022 | AMR | PUR | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG01192 | hp1 | a0002 | c0002 | t0001 | g0016 | AMR | PUR | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0168 | AMR | PUR | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0014 | AMR | PUR | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG01243 | hp2 | a0004 | c0005 | t0001 | g0003 | AMR | PUR | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG01257 | hp1 | a0001 | c0004 | t0001 | g0107 | AMR | CLM | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0228 | AMR | CLM | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0069 | AMR | CLM | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG01361 | hp1 | a0002 | c0002 | t0001 | g0174 | AMR | CLM | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG01361 | hp2 | a0002 | c0002 | t0001 | g0253 | AMR | CLM | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG01496 | hp1 | a0002 | c0002 | t0001 | g0003 | AMR | CLM | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG01516 | hp1 | a0002 | c0002 | t0001 | g0180 | EUR | IBS | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0008 | EUR | IBS | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG01517 | hp1 | a0002 | c0002 | t0001 | g0208 | EUR | IBS | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0008 | EUR | IBS | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | ACB | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG01884 | hp2 | a0001 | c0008 | t0002 | g0014 | AFR | ACB | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG01891 | hp1 | a0002 | c0002 | t0001 | g0239 | AFR | ACB | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG01891 | hp2 | a0002 | c0010 | t0001 | g0067 | AFR | ACB | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG01928 | hp2 | a0003 | c0003 | t0001 | g0007 | AMR | PEL | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG01934 | hp2 | a0001 | c0004 | t0001 | g0004 | AMR | PEL | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG01978 | hp1 | a0002 | c0002 | t0001 | g0016 | AMR | PEL | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG01978 | hp2 | a0003 | c0003 | t0001 | g0007 | AMR | PEL | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | PEL | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG01981 | hp2 | a0002 | c0002 | t0001 | g0216 | AMR | PEL | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG01993 | hp1 | a0003 | c0003 | t0001 | g0115 | AMR | PEL | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0090 | AMR | PEL | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG02004 | hp1 | a0003 | c0003 | t0001 | g0001 | AMR | PEL | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG02004 | hp2 | a0002 | c0002 | t0001 | g0206 | AMR | PEL | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | KHV | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | KHV | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | KHV | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG02027 | hp2 | a0002 | c0002 | t0001 | g0193 | EAS | KHV | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG02040 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | KHV | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | ACB | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0247 | AFR | ACB | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | KHV | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | KHV | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG02074 | hp2 | a0002 | c0002 | t0001 | g0184 | EAS | KHV | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG02129 | hp1 | a0003 | c0003 | t0001 | g0001 | EAS | KHV | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | KHV | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | KHV | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | KHV | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | KHV | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | ACB | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | ACB | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | PEL | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0238 | AMR | PEL | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | CDX | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG02165 | hp2 | a0002 | c0002 | t0001 | g0064 | EAS | CDX | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0230 | AFR | ACB | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG02257 | hp2 | a0002 | c0002 | t0001 | g0224 | AFR | ACB | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | ACB | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG02258 | hp2 | a0002 | c0002 | t0001 | g0013 | AFR | ACB | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0257 | AFR | ACB | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | ACB | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | PEL | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG02300 | hp1 | a0003 | c0003 | t0001 | g0112 | AMR | PEL | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG02300 | hp2 | a0002 | c0002 | t0001 | g0213 | AMR | PEL | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG02451 | hp1 | a0006 | c0011 | t0001 | g0024 | AFR | ACB | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0148 | AFR | ACB | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | GWD | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG02615 | hp2 | a0001 | c0001 | t0003 | g0161 | AFR | GWD | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0165 | AFR | GWD | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | GWD | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | GWD | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | GWD | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG02647 | hp2 | a0002 | c0002 | t0001 | g0013 | AFR | GWD | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG02698 | hp1 | a0002 | c0002 | t0001 | g0126 | SAS | PJL | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0121 | SAS | PJL | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | GWD | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0236 | AFR | GWD | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG02723 | hp1 | a0004 | c0005 | t0001 | g0003 | AFR | GWD | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG02809 | hp1 | a0004 | c0005 | t0001 | g0128 | AFR | GWD | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG02818 | hp1 | a0001 | c0006 | t0001 | g0070 | AFR | GWD | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG02818 | hp2 | a0004 | c0005 | t0001 | g0188 | AFR | GWD | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG02886 | hp1 | a0002 | c0002 | t0001 | g0256 | AFR | GWD | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | GWD | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | GWD | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0241 | AFR | GWD | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0218 | AFR | GWD | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | GWD | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | ESN | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0254 | AFR | ESN | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG02965 | hp1 | a0002 | c0002 | t0001 | g0012 | AFR | ESN | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | ESN | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | ESN | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG02970 | hp2 | a0001 | c0001 | t0003 | g0155 | AFR | ESN | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG02976 | hp1 | a0004 | c0005 | t0001 | g0186 | AFR | ESN | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0245 | AFR | ESN | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG03098 | hp1 | a0002 | c0002 | t0001 | g0255 | AFR | MSL | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0014 | AFR | MSL | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | ESN | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | ESN | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | ESN | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG03139 | hp2 | a0002 | c0002 | t0001 | g0013 | AFR | ESN | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | ESN | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0081 | AFR | MSL | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | MSL | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG03225 | hp1 | a0004 | c0005 | t0001 | g0189 | AFR | MSL | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | MSL | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG03239 | hp1 | a0001 | c0001 | t0003 | g0001 | SAS | PJL | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG03239 | hp2 | a0002 | c0002 | t0001 | g0187 | SAS | PJL | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG03453 | hp1 | a0002 | c0002 | t0001 | g0240 | AFR | MSL | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0166 | AFR | MSL | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | MSL | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | MSL | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG03490 | hp1 | a0002 | c0002 | t0001 | g0182 | SAS | PJL | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0026 | SAS | PJL | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG03491 | hp2 | a0002 | c0002 | t0001 | g0231 | SAS | PJL | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG03492 | hp1 | a0002 | c0002 | t0001 | g0233 | SAS | PJL | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0026 | SAS | PJL | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG03516 | hp1 | a0001 | c0006 | t0001 | g0248 | AFR | ESN | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | ESN | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | GWD | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | GWD | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | MSL | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | MSL | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG03654 | hp1 | a0002 | c0002 | t0001 | g0234 | SAS | PJL | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG03654 | hp2 | a0001 | c0001 | t0004 | g0227 | SAS | PJL | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG03669 | hp1 | a0002 | c0002 | t0001 | g0195 | SAS | PJL | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0158 | SAS | PJL | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG03688 | hp1 | a0002 | c0002 | t0001 | g0192 | SAS | STU | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG03688 | hp2 | a0001 | c0004 | t0001 | g0055 | SAS | STU | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG03704 | hp1 | a0001 | c0001 | t0004 | g0246 | SAS | PJL | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0052 | SAS | PJL | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0063 | SAS | BEB | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0062 | SAS | BEB | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG03834 | hp1 | a0002 | c0002 | t0001 | g0190 | SAS | BEB | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG03834 | hp2 | a0002 | c0002 | t0001 | g0220 | SAS | BEB | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG03927 | hp1 | a0001 | c0001 | t0004 | g0119 | SAS | BEB | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG03927 | hp2 | a0002 | c0002 | t0001 | g0221 | SAS | BEB | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG04115 | hp1 | a0001 | c0004 | t0001 | g0066 | SAS | STU | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG04115 | hp2 | a0002 | c0002 | t0001 | g0175 | SAS | STU | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | YRI | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| NA18522 | hp2 | a0001 | c0006 | t0001 | g0249 | AFR | YRI | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| NA18612 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | CHB | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | CHB | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| NA18747 | hp1 | a0002 | c0002 | t0001 | g0022 | EAS | CHB | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | CHB | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | YRI | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | YRI | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| NA18942 | hp1 | a0003 | c0003 | t0001 | g0001 | EAS | JPT | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| NA18944 | hp2 | a0002 | c0002 | t0001 | g0201 | EAS | JPT | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| NA18945 | hp2 | a0002 | c0002 | t0001 | g0079 | EAS | JPT | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| NA18948 | hp1 | a0002 | c0002 | t0001 | g0197 | EAS | JPT | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| NA18951 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| NA18952 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| NA18952 | hp2 | a0003 | c0003 | t0001 | g0001 | EAS | JPT | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| NA18957 | hp1 | a0002 | c0002 | t0001 | g0196 | EAS | JPT | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| NA18959 | hp1 | a0002 | c0002 | t0001 | g0130 | EAS | JPT | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| NA18961 | hp2 | a0002 | c0002 | t0001 | g0029 | EAS | JPT | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| NA18962 | hp1 | a0002 | c0002 | t0001 | g0204 | EAS | JPT | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| NA18963 | hp1 | a0002 | c0002 | t0001 | g0015 | EAS | JPT | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| NA18964 | hp1 | a0002 | c0002 | t0001 | g0242 | EAS | JPT | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| NA18964 | hp2 | a0002 | c0002 | t0001 | g0015 | EAS | JPT | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| NA18973 | hp2 | a0002 | c0002 | t0001 | g0179 | EAS | JPT | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| NA18979 | hp1 | a0007 | c0007 | t0001 | g0005 | EAS | JPT | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| NA18980 | hp1 | a0001 | c0014 | t0001 | g0006 | EAS | JPT | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| NA18984 | hp2 | a0002 | c0002 | t0001 | g0015 | EAS | JPT | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| NA18985 | hp2 | a0002 | c0002 | t0001 | g0211 | EAS | JPT | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| NA18991 | hp1 | a0002 | c0002 | t0001 | g0210 | EAS | JPT | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| NA18991 | hp2 | a0003 | c0003 | t0001 | g0001 | EAS | JPT | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| NA18992 | hp2 | a0002 | c0002 | t0001 | g0212 | EAS | JPT | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| NA18994 | hp1 | a0003 | c0003 | t0001 | g0007 | EAS | JPT | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| NA18999 | hp2 | a0003 | c0003 | t0001 | g0001 | EAS | JPT | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| NA19003 | hp2 | a0002 | c0002 | t0001 | g0080 | EAS | JPT | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| NA19004 | hp2 | a0002 | c0002 | t0001 | g0029 | EAS | JPT | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| NA19005 | hp1 | a0002 | c0002 | t0001 | g0194 | EAS | JPT | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| NA19007 | hp1 | a0002 | c0002 | t0001 | g0207 | EAS | JPT | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| NA19009 | hp1 | a0008 | c0009 | t0001 | g0198 | EAS | JPT | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | LWK | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0237 | AFR | LWK | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| NA19054 | hp1 | a0002 | c0002 | t0001 | g0243 | EAS | JPT | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| NA19060 | hp1 | a0002 | c0002 | t0001 | g0214 | EAS | JPT | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| NA19064 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| NA19068 | hp1 | a0002 | c0002 | t0001 | g0178 | EAS | JPT | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| NA19074 | hp1 | a0002 | c0002 | t0001 | g0127 | EAS | JPT | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| NA19078 | hp1 | a0002 | c0002 | t0001 | g0235 | EAS | JPT | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| NA19078 | hp2 | a0003 | c0003 | t0001 | g0162 | EAS | JPT | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| NA19079 | hp1 | a0002 | c0002 | t0001 | g0200 | EAS | JPT | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| NA19080 | hp1 | a0002 | c0002 | t0001 | g0199 | EAS | JPT | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| NA19081 | hp1 | a0002 | c0002 | t0001 | g0129 | EAS | JPT | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| NA19084 | hp2 | a0002 | c0002 | t0001 | g0217 | EAS | JPT | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| NA19091 | hp1 | a0002 | c0002 | t0001 | g0209 | EAS | JPT | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| NA19240 | hp1 | a0001 | c0006 | t0001 | g0030 | AFR | YRI | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | YRI | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0089 | SAS | GIH | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| NA20905 | hp2 | a0002 | c0002 | t0007 | g0215 | SAS | GIH | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG01123 | hp1 | a0002 | c0002 | t0001 | g0185 | AMR | CLM | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG02109 | hp1 | a0002 | c0002 | t0001 | g0003 | AFR | ACB | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | ACB | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | ACB | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG03471 | hp1 | a0002 | c0002 | t0001 | g0202 | AFR | MSL | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | MSL | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG06807 | hp1 | a0001 | c0006 | t0001 | g0030 | AFR | USA | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0229 | AFR | USA | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | LWK | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| NA21309 | hp2 | a0002 | c0002 | t0001 | g0191 | AFR | LWK | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| homoSapiens | chm13v2 | a0001 | c0012 | t0001 | g0002 | REF | REF | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| homoSapiens | grch38p0 | a0002 | c0002 | t0001 | g0003 | REF | REF | HERC5_chr4_88452119_88511163 | HERC5 | chr4 | 88452119 | 88511163 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:88463975 | G | A | 1 | a0004 | 6 | HG01243.hp2 HG02723.hp1 HG02809.hp1 others(3): Show |
missense_variant | MODERATE | c.901G>A | p.Ala301Thr | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 6/23 | 1052/3511 | 901/3075 | 301/1024 | chr4 | 88463975 | |||
| chr4:88463979 | G | C | 1 | a0003 | 13 | HG01109.hp1 HG01928.hp2 HG01978.hp2 others(10): Show |
missense_variant | MODERATE | c.905G>C | p.Cys302Ser | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 6/23 | 1056/3511 | 905/3075 | 302/1024 | chr4 | 88463979 | |||
| chr4:88467202 | T | C | 1 | a0007 | 1 | NA18979.hp1 | missense_variant&splice_region_variant | MODERATE | c.1055T>C | p.Leu352Pro | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 7/23 | 1206/3511 | 1055/3075 | 352/1024 | chr4 | 88467202 | |||
| chr4:88475940 | A | G | 4 | a0001 a0003 a0005 others(1): Show |
225 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(222): Show |
missense_variant | MODERATE | c.1492A>G | p.Met498Val | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 12/23 | 1643/3511 | 1492/3075 | 498/1024 | chr4 | 88475940 | |||
| chr4:88479361 | T | G | 1 | a0008 | 1 | NA19009.hp1 | missense_variant | MODERATE | c.1591T>G | p.Trp531Gly | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 13/23 | 1742/3511 | 1591/3075 | 531/1024 | chr4 | 88479361 | |||
| chr4:88493045 | G | A | 1 | a0006 | 1 | HG02451.hp1 | missense_variant | MODERATE | c.2167G>A | p.Gly723Arg | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 17/23 | 2318/3511 | 2167/3075 | 723/1024 | chr4 | 88493045 | |||
| chr4:88505856 | A | G | 1 | a0005 | 1 | HG00438.hp1 | missense_variant | MODERATE | c.3053A>G | p.Asn1018Ser | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 23/23 | 3204/3511 | 3053/3075 | 1018/1024 | chr4 | 88505856 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:88469243 | G | A | 1 | a0001c0008 | 1 | HG01884.hp2 | synonymous_variant | LOW | c.1221G>A | p.Arg407Arg | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 9/23 | 1372/3511 | 1221/3075 | 407/1024 | chr4 | 88469243 | |||
| chr4:88472445 | A | G | 1 | a0001c0006 | 5 | HG02818.hp1 HG03516.hp1 HG06807.hp1 others(2): Show |
synonymous_variant | LOW | c.1335A>G | p.Leu445Leu | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 11/23 | 1486/3511 | 1335/3075 | 445/1024 | chr4 | 88472445 | |||
| chr4:88486198 | A | G | 1 | a0001c0014 | 1 | NA18980.hp1 | synonymous_variant | LOW | c.1821A>G | p.Val607Val | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 14/23 | 1972/3511 | 1821/3075 | 607/1024 | chr4 | 88486198 | |||
| chr4:88489243 | G | A | 1 | a0002c0010 | 1 | HG01891.hp2 | synonymous_variant | LOW | c.2040G>A | p.Thr680Thr | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 16/23 | 2191/3511 | 2040/3075 | 680/1024 | chr4 | 88489243 | |||
| chr4:88499935 | A | G | 1 | a0001c0004 | 8 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(5): Show |
synonymous_variant | LOW | c.2454A>G | p.Gln818Gln | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 19/23 | 2605/3511 | 2454/3075 | 818/1024 | chr4 | 88499935 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:88457206 | G | C | 1 | a0002c0002t0006 | 1 | HG01099.hp2 | 5_prime_UTR_variant | MODIFIER | c.-64G>C | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 1/23 | 64 | chr4 | 88457206 | ||||||
| chr4:88505883 | C | T | 1 | a0002c0002t0007 | 1 | NA20905.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5C>T | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 23/23 | 5 | chr4 | 88505883 | ||||||
| chr4:88505908 | G | C | 2 | a0001c0001t0002 a0001c0008t0002 |
8 | HG01243.hp1 HG01884.hp2 HG02451.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*30G>C | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 23/23 | 30 | chr4 | 88505908 | ||||||
| chr4:88505919 | C | CGTT | 1 | a0001c0001t0003 | 3 | HG02615.hp2 HG02970.hp2 HG03239.hp1 |
3_prime_UTR_variant | MODIFIER | c.*66_*68dupGTT | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 23/23 | 69 | INFO_REALIGN_3_PRIME | chr4 | 88505919 | |||||
| chr4:88505919 | CGTT | C | 1 | a0002c0002t0005 | 3 | HG00140.hp1 HG00738.hp2 HG01069.hp2 |
3_prime_UTR_variant | MODIFIER | c.*66_*68delGTT | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 23/23 | 66 | INFO_REALIGN_3_PRIME | chr4 | 88505919 | |||||
| chr4:88506154 | G | A | 1 | a0001c0001t0004 | 3 | HG03654.hp2 HG03704.hp1 HG03927.hp1 |
3_prime_UTR_variant | MODIFIER | c.*276G>A | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 23/23 | 276 | chr4 | 88506154 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:88457542 | G | C | 1 | a0002c0002t0001g0031 | 1 | HG00738.hp1 | splice_region_variant&intron_variant | LOW | c.265+8G>C | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 1/22 | chr4 | 88457542 | |||||||
| chr4:88457597 | G | C | 2 | a0001c0001t0001g0032 a0001c0001t0001g0033 |
2 | NA18959.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.265+63G>C | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 1/22 | chr4 | 88457597 | |||||||
| chr4:88457609 | C | CG | 42 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(39): Show |
51 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(48): Show |
intron_variant | MODIFIER | c.265+80dupG | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | 88457609 | ||||||
| chr4:88457668 | A | T | 1 | a0001c0001t0001g0257 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.265+134A>T | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 1/22 | chr4 | 88457668 | |||||||
| chr4:88457708 | G | T | 2 | a0002c0002t0001g0255 a0002c0002t0001g0256 |
2 | HG02886.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.265+174G>T | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 1/22 | chr4 | 88457708 | |||||||
| chr4:88457815 | A | G | 1 | a0001c0001t0001g0254 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.265+281A>G | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 1/22 | chr4 | 88457815 | |||||||
| chr4:88457871 | G | A | 1 | a0001c0006t0001g0070 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.265+337G>A | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 1/22 | chr4 | 88457871 | |||||||
| chr4:88457992 | G | A | 6 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(3): Show |
6 | HG02280.hp2 HG02615.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.265+458G>A | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 1/22 | chr4 | 88457992 | |||||||
| chr4:88458396 | G | T | 1 | a0002c0002t0001g0253 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.265+862G>T | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 1/22 | chr4 | 88458396 | |||||||
| chr4:88458427 | C | T | 3 | a0001c0001t0001g0250 a0001c0001t0001g0251 a0001c0001t0001g0252 |
3 | NA18962.hp2 NA18985.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.265+893C>T | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 1/22 | chr4 | 88458427 | |||||||
| chr4:88458538 | T | G | 3 | a0001c0001t0001g0009 a0001c0001t0001g0077 a0001c0001t0001g0078 |
5 | HG01167.hp2 HG02723.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.266-809T>G | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 1/22 | chr4 | 88458538 | |||||||
| chr4:88458686 | T | C | 1 | a0001c0001t0001g0018 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.266-661T>C | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 1/22 | chr4 | 88458686 | |||||||
| chr4:88459319 | A | G | 4 | a0001c0006t0001g0030 a0001c0006t0001g0070 a0001c0006t0001g0248 others(1): Show |
5 | HG02818.hp1 HG03516.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.266-28A>G | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 1/22 | chr4 | 88459319 | |||||||
| chr4:88459613 | C | T | 1 | a0001c0001t0001g0247 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.389+143C>T | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 2/22 | chr4 | 88459613 | |||||||
| chr4:88459901 | A | T | 1 | a0001c0001t0004g0246 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.390-194A>T | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 2/22 | chr4 | 88459901 | |||||||
| chr4:88459958 | G | A | 1 | a0002c0002t0001g0079 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.390-137G>A | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 2/22 | chr4 | 88459958 | |||||||
| chr4:88460042 | A | G | 1 | a0001c0001t0001g0069 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.390-53A>G | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 2/22 | chr4 | 88460042 | |||||||
| chr4:88460945 | G | A | 1 | a0001c0001t0001g0034 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.466+774G>A | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 3/22 | chr4 | 88460945 | |||||||
| chr4:88461055 | G | A | 1 | a0002c0002t0001g0080 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.466+884G>A | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 3/22 | chr4 | 88461055 | |||||||
| chr4:88461164 | A | G | 1 | a0001c0001t0002g0245 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.467-971A>G | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 3/22 | chr4 | 88461164 | |||||||
| chr4:88461203 | T | C | 1 | a0001c0001t0002g0081 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.467-932T>C | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 3/22 | chr4 | 88461203 | |||||||
| chr4:88461560 | T | A | 1 | a0001c0001t0001g0082 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.467-575T>A | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 3/22 | chr4 | 88461560 | |||||||
| chr4:88461586 | C | T | 3 | a0002c0002t0001g0242 a0002c0002t0001g0243 a0002c0002t0001g0244 |
3 | HG00597.hp1 NA18964.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.467-549C>T | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 3/22 | chr4 | 88461586 | |||||||
| chr4:88461781 | G | A | 1 | a0001c0001t0001g0083 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.467-354G>A | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 3/22 | chr4 | 88461781 | |||||||
| chr4:88462101 | G | A | 2 | a0001c0001t0001g0084 a0001c0001t0001g0085 |
2 | HG01884.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.467-34G>A | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 3/22 | chr4 | 88462101 | |||||||
| chr4:88462511 | G | A | 23 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0082 others(20): Show |
32 | HG00621.hp2 HG00642.hp2 HG00741.hp2 others(29): Show |
intron_variant | MODIFIER | c.688+155G>A | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 4/22 | chr4 | 88462511 | |||||||
| chr4:88462570 | G | A | 2 | a0001c0001t0001g0102 a0001c0001t0001g0103 |
2 | NA18956.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.688+214G>A | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 4/22 | chr4 | 88462570 | |||||||
| chr4:88462958 | G | A | 1 | a0002c0002t0001g0104 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.689-574G>A | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 4/22 | chr4 | 88462958 | |||||||
| chr4:88463198 | A | C | 1 | a0001c0001t0001g0101 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.689-334A>C | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 4/22 | chr4 | 88463198 | |||||||
| chr4:88463768 | T | A | 2 | a0001c0001t0001g0034 a0001c0001t0001g0035 |
2 | NA19058.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.781-87T>A | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 5/22 | chr4 | 88463768 | |||||||
| chr4:88464057 | C | G | 1 | a0001c0001t0001g0241 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.911+72C>G | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 6/22 | chr4 | 88464057 | |||||||
| chr4:88464168 | A | AT | 8 | a0001c0001t0001g0068 a0001c0001t0001g0238 a0001c0001t0001g0247 others(5): Show |
8 | HG00438.hp2 HG00597.hp1 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.911+206dupT | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr4 | 88464168 | ||||||
| chr4:88464168 | AT | A | 75 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(72): Show |
99 | HG00408.hp1 HG00544.hp2 HG00621.hp1 others(96): Show |
intron_variant | MODIFIER | c.911+206delT | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr4 | 88464168 | ||||||
| chr4:88464186 | T | C | 1 | a0001c0001t0001g0036 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.911+201T>C | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 6/22 | chr4 | 88464186 | |||||||
| chr4:88464255 | G | A | 1 | a0001c0001t0001g0135 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.911+270G>A | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 6/22 | chr4 | 88464255 | |||||||
| chr4:88464561 | CTTGT | C | 3 | a0001c0001t0001g0018 a0001c0001t0001g0236 a0001c0001t0001g0237 |
4 | HG02717.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.911+595_911+598del others(4): Show |
HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr4 | 88464561 | ||||||
| chr4:88464761 | A | T | 2 | a0001c0001t0001g0018 a0001c0001t0001g0237 |
3 | HG02896.hp2 HG02897.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.911+776A>T | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 6/22 | chr4 | 88464761 | |||||||
| chr4:88464793 | C | T | 1 | a0001c0001t0001g0065 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.911+808C>T | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 6/22 | chr4 | 88464793 | |||||||
| chr4:88464913 | GGCGCCCG others(7): Show |
G | 1 | a0001c0001t0001g0045 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.911+931_911+944del others(14): Show |
HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr4 | 88464913 | ||||||
| chr4:88465012 | C | T | 1 | a0001c0001t0001g0044 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.911+1027C>T | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 6/22 | chr4 | 88465012 | |||||||
| chr4:88465025 | C | T | 2 | a0001c0001t0001g0133 a0001c0001t0001g0134 |
2 | NA18954.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.911+1040C>T | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 6/22 | chr4 | 88465025 | |||||||
| chr4:88465075 | C | T | 1 | a0002c0002t0001g0064 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.911+1090C>T | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 6/22 | chr4 | 88465075 | |||||||
| chr4:88465104 | G | A | 1 | a0001c0001t0001g0105 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.911+1119G>A | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 6/22 | chr4 | 88465104 | |||||||
| chr4:88465330 | C | G | 1 | a0001c0001t0001g0105 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.911+1345C>G | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 6/22 | chr4 | 88465330 | |||||||
| chr4:88465418 | G | T | 1 | a0002c0002t0001g0235 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.911+1433G>T | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 6/22 | chr4 | 88465418 | |||||||
| chr4:88465729 | A | C | 3 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0132 |
3 | HG02132.hp1 NA18946.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.912-1330A>C | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 6/22 | chr4 | 88465729 | |||||||
| chr4:88465861 | A | T | 1 | a0001c0001t0001g0100 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.912-1198A>T | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 6/22 | chr4 | 88465861 | |||||||
| chr4:88466089 | G | GT | 17 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0076 others(14): Show |
17 | HG00642.hp1 HG01257.hp2 HG01981.hp1 others(14): Show |
intron_variant | MODIFIER | c.912-955dupT | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr4 | 88466089 | ||||||
| chr4:88466142 | A | G | 1 | a0001c0001t0001g0075 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.912-917A>G | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 6/22 | chr4 | 88466142 | |||||||
| chr4:88466413 | T | C | 1 | a0001c0001t0001g0086 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.912-646T>C | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 6/22 | chr4 | 88466413 | |||||||
| chr4:88466439 | A | G | 6 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(3): Show |
6 | HG02280.hp2 HG02615.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.912-620A>G | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 6/22 | chr4 | 88466439 | |||||||
| chr4:88466620 | C | T | 1 | a0001c0001t0001g0099 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.912-439C>T | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 6/22 | chr4 | 88466620 | |||||||
| chr4:88466637 | A | G | 1 | a0001c0001t0001g0096 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.912-422A>G | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 6/22 | chr4 | 88466637 | |||||||
| chr4:88466991 | C | T | 2 | a0002c0002t0001g0224 a0002c0002t0006g0223 |
2 | HG01099.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.912-68C>T | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 6/22 | chr4 | 88466991 | |||||||
| chr4:88467417 | A | C | 7 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(4): Show |
7 | HG02055.hp2 HG02280.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1057+213A>C | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 7/22 | chr4 | 88467417 | |||||||
| chr4:88467471 | A | G | 1 | a0002c0002t0001g0222 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1057+267A>G | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 7/22 | chr4 | 88467471 | |||||||
| chr4:88467774 | G | A | 4 | a0001c0001t0001g0046 a0001c0001t0001g0048 a0001c0001t0001g0106 others(1): Show |
4 | HG00438.hp1 NA18942.hp2 NA18950.hp2 others(1): Show |
intron_variant | MODIFIER | c.1057+570G>A | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 7/22 | chr4 | 88467774 | |||||||
| chr4:88467923 | T | A | 44 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(41): Show |
54 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(51): Show |
intron_variant | MODIFIER | c.1058-423T>A | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 7/22 | chr4 | 88467923 | |||||||
| chr4:88468255 | G | A | 1 | a0001c0001t0001g0097 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1058-91G>A | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 7/22 | chr4 | 88468255 | |||||||
| chr4:88468264 | G | C | 1 | a0001c0001t0001g0236 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1058-82G>C | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 7/22 | chr4 | 88468264 | |||||||
| chr4:88468323 | T | G | 19 | a0001c0001t0001g0009 a0001c0001t0001g0024 a0001c0001t0001g0025 others(16): Show |
23 | HG01167.hp2 HG01884.hp1 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.1058-23T>G | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 7/22 | chr4 | 88468323 | |||||||
| chr4:88468489 | C | A | 180 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(177): Show |
227 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(224): Show |
intron_variant | MODIFIER | c.1134+67C>A | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 8/22 | chr4 | 88468489 | |||||||
| chr4:88468639 | T | C | 4 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0099 others(1): Show |
4 | NA18961.hp1 NA18988.hp2 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.1134+217T>C | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 8/22 | chr4 | 88468639 | |||||||
| chr4:88468747 | C | T | 12 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0168 others(9): Show |
14 | HG01167.hp1 HG01169.hp2 HG01192.hp2 others(11): Show |
intron_variant | MODIFIER | c.1134+325C>T | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 8/22 | chr4 | 88468747 | |||||||
| chr4:88468837 | C | T | 1 | a0002c0002t0001g0234 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1135-320C>T | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 8/22 | chr4 | 88468837 | |||||||
| chr4:88469014 | G | T | 1 | a0002c0002t0001g0221 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1135-143G>T | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 8/22 | chr4 | 88469014 | |||||||
| chr4:88469445 | A | G | 1 | a0001c0001t0001g0228 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1238+185A>G | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 9/22 | chr4 | 88469445 | |||||||
| chr4:88469528 | C | A | 3 | a0002c0002t0001g0242 a0002c0002t0001g0243 a0002c0002t0001g0244 |
3 | HG00597.hp1 NA18964.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.1238+268C>A | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 9/22 | chr4 | 88469528 | |||||||
| chr4:88469667 | T | C | 2 | a0001c0001t0001g0019 a0001c0001t0001g0108 |
3 | NA18612.hp2 NA18983.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.1238+407T>C | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 9/22 | chr4 | 88469667 | |||||||
| chr4:88469838 | A | G | 1 | a0001c0001t0001g0147 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1238+578A>G | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 9/22 | chr4 | 88469838 | |||||||
| chr4:88469986 | C | G | 2 | a0001c0001t0001g0018 a0001c0001t0001g0237 |
3 | HG02896.hp2 HG02897.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1239-628C>G | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 9/22 | chr4 | 88469986 | |||||||
| chr4:88470389 | C | G | 3 | a0002c0002t0001g0220 a0002c0002t0001g0255 a0002c0002t0001g0256 |
3 | HG02886.hp1 HG03098.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.1239-225C>G | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 9/22 | chr4 | 88470389 | |||||||
| chr4:88470408 | T | C | 1 | a0001c0001t0002g0148 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1239-206T>C | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 9/22 | chr4 | 88470408 | |||||||
| chr4:88470420 | T | G | 1 | a0001c0001t0002g0148 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1239-194T>G | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 9/22 | chr4 | 88470420 | |||||||
| chr4:88470774 | T | G | 1 | a0001c0001t0001g0254 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1298+101T>G | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 10/22 | chr4 | 88470774 | |||||||
| chr4:88470835 | C | T | 1 | a0001c0001t0001g0167 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1298+162C>T | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 10/22 | chr4 | 88470835 | |||||||
| chr4:88470890 | C | T | 1 | a0002c0002t0001g0219 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1298+217C>T | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 10/22 | chr4 | 88470890 | |||||||
| chr4:88470975 | C | CT | 15 | a0001c0001t0001g0009 a0001c0001t0001g0025 a0001c0001t0001g0026 others(12): Show |
19 | HG01106.hp1 HG01167.hp2 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.1298+313dupT | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr4 | 88470975 | ||||||
| chr4:88471008 | G | A | 1 | a0001c0001t0001g0241 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1298+335G>A | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 10/22 | chr4 | 88471008 | |||||||
| chr4:88471148 | T | C | 1 | a0001c0001t0001g0149 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1298+475T>C | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 10/22 | chr4 | 88471148 | |||||||
| chr4:88471171 | T | C | 1 | a0002c0002t0006g0223 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1298+498T>C | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 10/22 | chr4 | 88471171 | |||||||
| chr4:88471190 | G | A | 6 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(3): Show |
6 | HG02280.hp2 HG02615.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1298+517G>A | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 10/22 | chr4 | 88471190 | |||||||
| chr4:88471284 | A | C | 8 | a0001c0001t0001g0218 a0001c0001t0002g0014 a0001c0001t0002g0081 others(5): Show |
9 | HG01243.hp1 HG01884.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1298+611A>C | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 10/22 | chr4 | 88471284 | |||||||
| chr4:88471844 | G | C | 1 | a0002c0002t0001g0174 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1299-565G>C | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 10/22 | chr4 | 88471844 | |||||||
| chr4:88471897 | C | T | 36 | a0001c0001t0001g0005 a0002c0002t0001g0005 a0002c0002t0001g0064 others(33): Show |
39 | HG00423.hp2 HG00544.hp1 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.1299-512C>T | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 10/22 | chr4 | 88471897 | |||||||
| chr4:88471927 | G | A | 1 | a0001c0001t0001g0042 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1299-482G>A | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 10/22 | chr4 | 88471927 | |||||||
| chr4:88471930 | C | T | 2 | a0001c0001t0001g0021 a0001c0001t0001g0125 |
3 | HG00408.hp1 HG02015.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.1299-479C>T | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 10/22 | chr4 | 88471930 | |||||||
| chr4:88472014 | G | A | 1 | a0001c0001t0001g0150 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1299-395G>A | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 10/22 | chr4 | 88472014 | |||||||
| chr4:88472017 | G | A | 2 | a0001c0001t0001g0142 a0001c0001t0001g0143 |
2 | HG02922.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1299-392G>A | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 10/22 | chr4 | 88472017 | |||||||
| chr4:88472329 | G | A | 1 | a0002c0002t0001g0195 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1299-80G>A | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 10/22 | chr4 | 88472329 | |||||||
| chr4:88472704 | T | A | 2 | a0001c0001t0001g0011 a0001c0001t0001g0151 |
4 | HG02145.hp1 HG02559.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1392+202T>A | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 11/22 | chr4 | 88472704 | |||||||
| chr4:88472712 | ATAGTGTG others(5): Show |
A | 2 | a0001c0001t0001g0011 a0001c0001t0001g0151 |
4 | HG02145.hp1 HG02559.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1392+211_1392+222d others(14): Show |
HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 11/22 | chr4 | 88472712 | |||||||
| chr4:88472755 | A | G | 46 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(43): Show |
56 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(53): Show |
intron_variant | MODIFIER | c.1392+253A>G | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 11/22 | chr4 | 88472755 | |||||||
| chr4:88472757 | A | G | 7 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(4): Show |
7 | HG02055.hp2 HG02280.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1392+255A>G | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 11/22 | chr4 | 88472757 | |||||||
| chr4:88472921 | C | CT | 6 | a0001c0001t0001g0063 a0001c0001t0001g0094 a0001c0004t0001g0107 others(3): Show |
6 | HG01257.hp1 HG01981.hp2 HG02135.hp1 others(3): Show |
intron_variant | MODIFIER | c.1392+436dupT | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr4 | 88472921 | ||||||
| chr4:88472921 | CT | C | 19 | a0001c0001t0001g0009 a0001c0001t0001g0025 a0001c0001t0001g0027 others(16): Show |
23 | HG01167.hp1 HG01167.hp2 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.1392+436delT | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr4 | 88472921 | ||||||
| chr4:88472934 | T | C | 6 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(3): Show |
6 | HG02280.hp2 HG02615.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1392+432T>C | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 11/22 | chr4 | 88472934 | |||||||
| chr4:88473027 | G | A | 1 | a0002c0002t0001g0175 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1392+525G>A | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 11/22 | chr4 | 88473027 | |||||||
| chr4:88473051 | A | G | 1 | a0001c0001t0001g0124 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1392+549A>G | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 11/22 | chr4 | 88473051 | |||||||
| chr4:88473130 | G | A | 1 | a0001c0001t0001g0049 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.1392+628G>A | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 11/22 | chr4 | 88473130 | |||||||
| chr4:88473599 | C | G | 1 | a0001c0001t0001g0124 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1392+1097C>G | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 11/22 | chr4 | 88473599 | |||||||
| chr4:88473613 | G | A | 4 | a0001c0001t0001g0152 a0001c0001t0001g0154 a0001c0001t0001g0167 others(1): Show |
4 | HG02280.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1392+1111G>A | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 11/22 | chr4 | 88473613 | |||||||
| chr4:88473813 | G | T | 19 | a0001c0001t0001g0009 a0001c0001t0001g0024 a0001c0001t0001g0025 others(16): Show |
23 | HG01167.hp2 HG01884.hp1 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.1392+1311G>T | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 11/22 | chr4 | 88473813 | |||||||
| chr4:88473904 | T | C | 3 | a0001c0001t0001g0046 a0001c0001t0001g0106 a0005c0013t0001g0047 |
3 | HG00438.hp1 NA18950.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.1392+1402T>C | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 11/22 | chr4 | 88473904 | |||||||
| chr4:88473999 | C | T | 2 | a0001c0001t0001g0011 a0001c0001t0001g0151 |
4 | HG02145.hp1 HG02559.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1392+1497C>T | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 11/22 | chr4 | 88473999 | |||||||
| chr4:88474281 | G | A | 1 | a0001c0001t0001g0257 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1393-1560G>A | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 11/22 | chr4 | 88474281 | |||||||
| chr4:88474497 | G | A | 2 | a0002c0002t0001g0012 a0002c0002t0001g0013 |
6 | HG00639.hp2 HG01109.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.1393-1344G>A | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 11/22 | chr4 | 88474497 | |||||||
| chr4:88474538 | C | T | 1 | a0002c0002t0007g0215 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1393-1303C>T | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 11/22 | chr4 | 88474538 | |||||||
| chr4:88475117 | C | CT | 37 | a0001c0001t0001g0025 a0001c0001t0001g0027 a0001c0001t0001g0028 others(34): Show |
40 | HG00621.hp1 HG01167.hp1 HG01169.hp2 others(37): Show |
intron_variant | MODIFIER | c.1393-708dupT | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr4 | 88475117 | ||||||
| chr4:88475323 | T | G | 1 | a0001c0001t0001g0236 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1393-518T>G | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 11/22 | chr4 | 88475323 | |||||||
| chr4:88475324 | C | CT | 18 | a0001c0001t0001g0042 a0001c0001t0001g0083 a0001c0001t0001g0092 others(15): Show |
18 | HG00621.hp1 HG01192.hp2 HG02132.hp1 others(15): Show |
intron_variant | MODIFIER | c.1393-499dupT | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr4 | 88475324 | ||||||
| chr4:88475324 | CT | C | 41 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(38): Show |
51 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(48): Show |
intron_variant | MODIFIER | c.1393-499delT | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr4 | 88475324 | ||||||
| chr4:88475537 | A | ACGATCTC others(17): Show |
1 | a0002c0002t0001g0216 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1393-302_1393-279d others(26): Show |
HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr4 | 88475537 | ||||||
| chr4:88476185 | G | A | 2 | a0002c0002t0001g0031 a0002c0002t0005g0176 |
2 | HG00738.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1582+155G>A | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 12/22 | chr4 | 88476185 | |||||||
| chr4:88476443 | T | G | 1 | a0001c0001t0001g0075 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1582+413T>G | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 12/22 | chr4 | 88476443 | |||||||
| chr4:88476499 | G | A | 1 | a0002c0002t0001g0195 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1582+469G>A | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 12/22 | chr4 | 88476499 | |||||||
| chr4:88476709 | T | A | 4 | a0001c0001t0001g0152 a0001c0001t0001g0154 a0001c0001t0001g0167 others(1): Show |
4 | HG02280.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1582+679T>A | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 12/22 | chr4 | 88476709 | |||||||
| chr4:88476759 | A | G | 5 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0041 others(2): Show |
7 | HG00408.hp1 HG02015.hp1 HG03491.hp1 others(4): Show |
intron_variant | MODIFIER | c.1582+729A>G | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 12/22 | chr4 | 88476759 | |||||||
| chr4:88476813 | C | T | 2 | a0001c0001t0001g0173 a0001c0001t0001g0236 |
2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1582+783C>T | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 12/22 | chr4 | 88476813 | |||||||
| chr4:88476877 | G | A | 2 | a0001c0001t0001g0037 a0001c0001t0001g0050 |
2 | NA18946.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.1582+847G>A | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 12/22 | chr4 | 88476877 | |||||||
| chr4:88476919 | C | CA | 12 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0163 others(9): Show |
14 | HG01167.hp1 HG01169.hp2 HG01192.hp2 others(11): Show |
intron_variant | MODIFIER | c.1582+899dupA | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr4 | 88476919 | ||||||
| chr4:88476920 | A | C | 1 | a0004c0005t0001g0189 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1582+890A>C | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 12/22 | chr4 | 88476920 | |||||||
| chr4:88477014 | G | A | 63 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(60): Show |
76 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(73): Show |
intron_variant | MODIFIER | c.1582+984G>A | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 12/22 | chr4 | 88477014 | |||||||
| chr4:88477029 | C | T | 1 | a0002c0002t0001g0222 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1582+999C>T | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 12/22 | chr4 | 88477029 | |||||||
| chr4:88477064 | C | CT | 69 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(66): Show |
85 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.1582+1050dupT | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr4 | 88477064 | ||||||
| chr4:88477064 | C | CTT | 10 | a0001c0001t0001g0027 a0001c0001t0001g0035 a0001c0001t0001g0059 others(7): Show |
11 | HG01167.hp1 HG01169.hp2 HG02148.hp2 others(8): Show |
intron_variant | MODIFIER | c.1582+1049_1582+105 others(6): Show |
HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr4 | 88477064 | ||||||
| chr4:88477064 | CT | C | 6 | a0001c0001t0001g0149 a0001c0001t0001g0250 a0002c0002t0001g0080 others(3): Show |
6 | HG00280.hp2 HG00597.hp2 NA18948.hp1 others(3): Show |
intron_variant | MODIFIER | c.1582+1050delT | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr4 | 88477064 | ||||||
| chr4:88477267 | GAGGGAAG others(4): Show |
G | 5 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0041 others(2): Show |
7 | HG00408.hp1 HG02015.hp1 HG03491.hp1 others(4): Show |
intron_variant | MODIFIER | c.1582+1253_1582+126 others(15): Show |
HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr4 | 88477267 | ||||||
| chr4:88477280 | G | A | 1 | a0001c0001t0001g0069 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1582+1250G>A | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 12/22 | chr4 | 88477280 | |||||||
| chr4:88477283 | A | G | 1 | a0001c0001t0003g0161 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1582+1253A>G | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 12/22 | chr4 | 88477283 | |||||||
| chr4:88477326 | GA | G | 3 | a0001c0001t0001g0091 a0001c0001t0001g0097 a0001c0001t0001g0098 |
3 | HG00621.hp2 HG02015.hp2 HG02129.hp2 |
intron_variant | MODIFIER | c.1582+1297delA | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 12/22 | chr4 | 88477326 | |||||||
| chr4:88477327 | AG | A | 47 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0020 others(44): Show |
60 | HG00408.hp1 HG00544.hp2 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.1582+1302delG | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr4 | 88477327 | ||||||
| chr4:88477332 | G | A | 1 | a0001c0001t0001g0110 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1582+1302G>A | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 12/22 | chr4 | 88477332 | |||||||
| chr4:88477333 | A | G | 2 | a0001c0001t0001g0058 a0001c0001t0001g0110 |
2 | NA18956.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.1582+1303A>G | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 12/22 | chr4 | 88477333 | |||||||
| chr4:88477339 | G | A | 1 | a0001c0001t0001g0167 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1582+1309G>A | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 12/22 | chr4 | 88477339 | |||||||
| chr4:88477374 | G | A | 2 | a0001c0001t0001g0037 a0001c0001t0001g0050 |
2 | NA18946.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.1582+1344G>A | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 12/22 | chr4 | 88477374 | |||||||
| chr4:88477439 | C | G | 169 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(166): Show |
211 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(208): Show |
intron_variant | MODIFIER | c.1582+1409C>G | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 12/22 | chr4 | 88477439 | |||||||
| chr4:88478058 | A | G | 1 | a0002c0002t0001g0222 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1583-1295A>G | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 12/22 | chr4 | 88478058 | |||||||
| chr4:88478286 | A | G | 6 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0001g0139 others(3): Show |
6 | HG02109.hp2 HG02145.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.1583-1067A>G | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 12/22 | chr4 | 88478286 | |||||||
| chr4:88478616 | A | T | 1 | a0001c0001t0001g0252 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1583-737A>T | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 12/22 | chr4 | 88478616 | |||||||
| chr4:88478617 | T | A | 1 | a0001c0001t0001g0252 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1583-736T>A | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 12/22 | chr4 | 88478617 | |||||||
| chr4:88478618 | A | T | 1 | a0001c0001t0001g0252 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1583-735A>T | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 12/22 | chr4 | 88478618 | |||||||
| chr4:88478710 | C | G | 1 | a0001c0001t0002g0166 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1583-643C>G | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 12/22 | chr4 | 88478710 | |||||||
| chr4:88479002 | A | G | 3 | a0001c0001t0001g0057 a0001c0001t0001g0060 a0001c0001t0001g0065 |
3 | HG02056.hp2 HG02165.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.1583-351A>G | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 12/22 | chr4 | 88479002 | |||||||
| chr4:88479284 | C | CA | 22 | a0001c0001t0001g0035 a0001c0001t0001g0051 a0001c0001t0001g0058 others(19): Show |
22 | HG01981.hp1 HG02027.hp2 HG02148.hp2 others(19): Show |
intron_variant | MODIFIER | c.1583-51dupA | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr4 | 88479284 | ||||||
| chr4:88479284 | CA | C | 6 | a0001c0001t0001g0061 a0001c0001t0004g0119 a0001c0001t0004g0227 others(3): Show |
6 | HG03654.hp2 HG03704.hp1 HG03927.hp1 others(3): Show |
intron_variant | MODIFIER | c.1583-51delA | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr4 | 88479284 | ||||||
| chr4:88479323 | T | A | 1 | a0002c0002t0001g0190 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1583-30T>A | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 12/22 | chr4 | 88479323 | |||||||
| chr4:88479534 | G | T | 7 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(4): Show |
7 | HG02055.hp2 HG02280.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1737+27G>T | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 13/22 | chr4 | 88479534 | |||||||
| chr4:88479630 | T | A | 1 | a0001c0001t0001g0063 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1737+123T>A | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 13/22 | chr4 | 88479630 | |||||||
| chr4:88479648 | ACAT | A | 72 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(69): Show |
95 | HG00408.hp1 HG00544.hp2 HG00597.hp2 others(92): Show |
intron_variant | MODIFIER | c.1737+145_1737+147d others(5): Show |
HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr4 | 88479648 | ||||||
| chr4:88479796 | G | A | 66 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(63): Show |
82 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.1737+289G>A | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 13/22 | chr4 | 88479796 | |||||||
| chr4:88479811 | T | A | 1 | a0002c0002t0001g0178 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1737+304T>A | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 13/22 | chr4 | 88479811 | |||||||
| chr4:88479923 | T | A | 2 | a0001c0001t0001g0072 a0001c0001t0001g0076 |
2 | HG02615.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1737+416T>A | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 13/22 | chr4 | 88479923 | |||||||
| chr4:88480039 | C | G | 1 | a0001c0001t0001g0041 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1737+532C>G | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 13/22 | chr4 | 88480039 | |||||||
| chr4:88480066 | CA | C | 160 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(157): Show |
202 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(199): Show |
intron_variant | MODIFIER | c.1737+578delA | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr4 | 88480066 | ||||||
| chr4:88480189 | C | T | 3 | a0001c0001t0001g0153 a0001c0001t0001g0228 a0001c0006t0001g0070 |
3 | HG01257.hp2 HG02630.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1737+682C>T | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 13/22 | chr4 | 88480189 | |||||||
| chr4:88480444 | G | GT | 72 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(69): Show |
96 | HG00408.hp1 HG00544.hp2 HG00597.hp2 others(93): Show |
intron_variant | MODIFIER | c.1737+949dupT | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr4 | 88480444 | ||||||
| chr4:88480446 | T | G | 1 | a0001c0001t0001g0075 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1737+939T>G | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 13/22 | chr4 | 88480446 | |||||||
| chr4:88480918 | T | C | 1 | a0001c0001t0001g0076 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1737+1411T>C | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 13/22 | chr4 | 88480918 | |||||||
| chr4:88480958 | A | G | 1 | a0001c0001t0001g0056 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1737+1451A>G | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 13/22 | chr4 | 88480958 | |||||||
| chr4:88481041 | C | A | 1 | a0001c0001t0002g0166 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1737+1534C>A | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 13/22 | chr4 | 88481041 | |||||||
| chr4:88481128 | C | T | 3 | a0001c0006t0001g0030 a0001c0006t0001g0248 a0001c0006t0001g0249 |
4 | HG03516.hp1 HG06807.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1737+1621C>T | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 13/22 | chr4 | 88481128 | |||||||
| chr4:88481472 | G | C | 1 | a0002c0002t0006g0223 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1737+1965G>C | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 13/22 | chr4 | 88481472 | |||||||
| chr4:88482047 | T | G | 171 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(168): Show |
213 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(210): Show |
intron_variant | MODIFIER | c.1737+2540T>G | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 13/22 | chr4 | 88482047 | |||||||
| chr4:88482235 | A | C | 1 | a0001c0001t0001g0141 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1737+2728A>C | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 13/22 | chr4 | 88482235 | |||||||
| chr4:88482267 | G | A | 1 | a0002c0002t0001g0180 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1737+2760G>A | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 13/22 | chr4 | 88482267 | |||||||
| chr4:88482309 | C | CA | 11 | a0001c0001t0001g0053 a0001c0001t0001g0078 a0001c0001t0001g0108 others(8): Show |
11 | HG00735.hp1 HG00741.hp1 HG03516.hp2 others(8): Show |
intron_variant | MODIFIER | c.1737+2817dupA | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr4 | 88482309 | ||||||
| chr4:88482751 | T | G | 8 | a0001c0001t0001g0218 a0001c0001t0002g0014 a0001c0001t0002g0081 others(5): Show |
9 | HG01243.hp1 HG01884.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1737+3244T>G | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 13/22 | chr4 | 88482751 | |||||||
| chr4:88482984 | G | C | 1 | a0002c0002t0001g0220 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1738-3131G>C | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 13/22 | chr4 | 88482984 | |||||||
| chr4:88483200 | A | G | 3 | a0002c0002t0001g0255 a0002c0002t0001g0256 a0002c0010t0001g0067 |
3 | HG01891.hp2 HG02886.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1738-2915A>G | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 13/22 | chr4 | 88483200 | |||||||
| chr4:88483211 | CTGT | C | 4 | a0001c0001t0001g0152 a0001c0001t0001g0154 a0001c0001t0001g0167 others(1): Show |
4 | HG02280.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1738-2890_1738-288 others(7): Show |
HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr4 | 88483211 | ||||||
| chr4:88483214 | T | C | 1 | a0001c0001t0001g0113 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1738-2901T>C | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 13/22 | chr4 | 88483214 | |||||||
| chr4:88483321 | A | G | 1 | a0001c0001t0001g0237 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1738-2794A>G | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 13/22 | chr4 | 88483321 | |||||||
| chr4:88483408 | A | G | 4 | a0001c0006t0001g0030 a0001c0006t0001g0070 a0001c0006t0001g0248 others(1): Show |
5 | HG02818.hp1 HG03516.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.1738-2707A>G | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 13/22 | chr4 | 88483408 | |||||||
| chr4:88483519 | C | CT | 76 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0058 others(73): Show |
88 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(85): Show |
intron_variant | MODIFIER | c.1738-2572dupT | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr4 | 88483519 | ||||||
| chr4:88483635 | C | T | 1 | a0001c0001t0001g0075 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1738-2480C>T | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 13/22 | chr4 | 88483635 | |||||||
| chr4:88483639 | G | A | 1 | a0001c0001t0001g0111 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1738-2476G>A | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 13/22 | chr4 | 88483639 | |||||||
| chr4:88484051 | C | T | 1 | a0001c0004t0001g0054 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1738-2064C>T | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 13/22 | chr4 | 88484051 | |||||||
| chr4:88484478 | T | C | 1 | a0002c0002t0001g0181 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1738-1637T>C | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 13/22 | chr4 | 88484478 | |||||||
| chr4:88484866 | A | T | 1 | a0001c0001t0001g0241 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1738-1249A>T | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 13/22 | chr4 | 88484866 | |||||||
| chr4:88485039 | G | GT | 11 | a0001c0001t0001g0116 a0001c0001t0001g0118 a0001c0001t0001g0125 others(8): Show |
11 | HG00408.hp1 HG01981.hp2 HG02027.hp2 others(8): Show |
intron_variant | MODIFIER | c.1738-1064dupT | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr4 | 88485039 | ||||||
| chr4:88485225 | C | T | 1 | a0002c0002t0006g0223 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1738-890C>T | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 13/22 | chr4 | 88485225 | |||||||
| chr4:88485502 | T | C | 1 | a0002c0002t0001g0224 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1738-613T>C | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 13/22 | chr4 | 88485502 | |||||||
| chr4:88485834 | G | GT | 5 | a0001c0001t0001g0035 a0001c0006t0001g0030 a0001c0006t0001g0070 others(2): Show |
6 | HG02818.hp1 HG03516.hp1 HG06807.hp1 others(3): Show |
intron_variant | MODIFIER | c.1738-270dupT | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr4 | 88485834 | ||||||
| chr4:88486053 | C | T | 1 | a0001c0001t0001g0254 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1738-62C>T | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 13/22 | chr4 | 88486053 | |||||||
| chr4:88486360 | C | T | 1 | a0001c0001t0001g0167 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1851+132C>T | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 14/22 | chr4 | 88486360 | |||||||
| chr4:88486576 | G | A | 1 | a0002c0002t0001g0174 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1851+348G>A | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 14/22 | chr4 | 88486576 | |||||||
| chr4:88486699 | A | G | 1 | a0002c0002t0001g0211 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1852-370A>G | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 14/22 | chr4 | 88486699 | |||||||
| chr4:88487451 | C | T | 4 | a0001c0006t0001g0030 a0001c0006t0001g0070 a0001c0006t0001g0248 others(1): Show |
5 | HG02818.hp1 HG03516.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.1962+272C>T | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 15/22 | chr4 | 88487451 | |||||||
| chr4:88487906 | C | A | 2 | a0002c0002t0001g0015 a0002c0002t0001g0179 |
4 | NA18963.hp1 NA18964.hp2 NA18973.hp2 others(1): Show |
intron_variant | MODIFIER | c.1962+727C>A | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 15/22 | chr4 | 88487906 | |||||||
| chr4:88488052 | G | A | 1 | a0001c0001t0001g0237 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1962+873G>A | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 15/22 | chr4 | 88488052 | |||||||
| chr4:88488124 | C | T | 2 | a0002c0002t0001g0012 a0002c0002t0001g0013 |
6 | HG00639.hp2 HG01109.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.1962+945C>T | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 15/22 | chr4 | 88488124 | |||||||
| chr4:88488155 | A | T | 15 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0163 others(12): Show |
17 | HG01167.hp1 HG01169.hp2 HG01192.hp2 others(14): Show |
intron_variant | MODIFIER | c.1962+976A>T | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 15/22 | chr4 | 88488155 | |||||||
| chr4:88488234 | C | CT | 6 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0108 others(3): Show |
8 | HG01517.hp1 HG02004.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.1963-917dupT | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr4 | 88488234 | ||||||
| chr4:88488239 | T | C | 1 | a0001c0001t0001g0036 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1963-927T>C | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 15/22 | chr4 | 88488239 | |||||||
| chr4:88488580 | T | C | 1 | a0003c0003t0001g0112 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1963-586T>C | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 15/22 | chr4 | 88488580 | |||||||
| chr4:88488829 | A | G | 1 | a0001c0001t0001g0088 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1963-337A>G | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 15/22 | chr4 | 88488829 | |||||||
| chr4:88488986 | C | T | 1 | a0001c0001t0001g0140 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1963-180C>T | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 15/22 | chr4 | 88488986 | |||||||
| chr4:88489623 | C | G | 2 | a0001c0001t0001g0145 a0001c0001t0001g0146 |
2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2133+287C>G | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 16/22 | chr4 | 88489623 | |||||||
| chr4:88489639 | A | G | 1 | a0002c0002t0001g0205 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.2133+303A>G | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 16/22 | chr4 | 88489639 | |||||||
| chr4:88489742 | C | T | 2 | a0001c0001t0001g0173 a0001c0001t0001g0236 |
2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.2133+406C>T | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 16/22 | chr4 | 88489742 | |||||||
| chr4:88489879 | G | A | 1 | a0001c0004t0001g0055 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2133+543G>A | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 16/22 | chr4 | 88489879 | |||||||
| chr4:88489975 | T | C | 167 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(164): Show |
209 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(206): Show |
intron_variant | MODIFIER | c.2133+639T>C | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 16/22 | chr4 | 88489975 | |||||||
| chr4:88489985 | G | A | 1 | a0001c0001t0001g0105 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.2133+649G>A | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 16/22 | chr4 | 88489985 | |||||||
| chr4:88490924 | G | A | 1 | a0001c0001t0001g0158 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2133+1588G>A | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 16/22 | chr4 | 88490924 | |||||||
| chr4:88490943 | A | G | 2 | a0002c0002t0001g0231 a0002c0002t0001g0233 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.2133+1607A>G | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 16/22 | chr4 | 88490943 | |||||||
| chr4:88491186 | T | A | 1 | a0001c0001t0001g0089 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2134-1826T>A | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 16/22 | chr4 | 88491186 | |||||||
| chr4:88491378 | C | A | 1 | a0001c0006t0001g0249 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2134-1634C>A | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 16/22 | chr4 | 88491378 | |||||||
| chr4:88491543 | G | T | 1 | a0001c0001t0001g0241 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.2134-1469G>T | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 16/22 | chr4 | 88491543 | |||||||
| chr4:88491594 | A | G | 1 | a0002c0002t0001g0219 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.2134-1418A>G | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 16/22 | chr4 | 88491594 | |||||||
| chr4:88491611 | T | A | 1 | a0001c0006t0001g0070 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2134-1401T>A | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 16/22 | chr4 | 88491611 | |||||||
| chr4:88491869 | A | G | 1 | a0002c0002t0001g0211 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.2134-1143A>G | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 16/22 | chr4 | 88491869 | |||||||
| chr4:88491961 | A | G | 4 | a0001c0001t0001g0152 a0001c0001t0001g0154 a0001c0001t0001g0167 others(1): Show |
4 | HG02280.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.2134-1051A>G | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 16/22 | chr4 | 88491961 | |||||||
| chr4:88492099 | G | A | 3 | a0001c0001t0001g0171 a0001c0001t0003g0155 a0001c0001t0003g0161 |
3 | HG02615.hp2 HG02970.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2134-913G>A | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 16/22 | chr4 | 88492099 | |||||||
| chr4:88492192 | C | T | 1 | a0002c0002t0005g0176 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.2134-820C>T | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 16/22 | chr4 | 88492192 | |||||||
| chr4:88492193 | G | A | 2 | a0002c0002t0001g0231 a0002c0002t0001g0233 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.2134-819G>A | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 16/22 | chr4 | 88492193 | |||||||
| chr4:88492299 | C | T | 12 | a0001c0001t0001g0009 a0001c0001t0001g0025 a0001c0001t0001g0077 others(9): Show |
15 | HG01167.hp2 HG01884.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.2134-713C>T | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 16/22 | chr4 | 88492299 | |||||||
| chr4:88492393 | C | A | 1 | a0001c0004t0001g0055 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2134-619C>A | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 16/22 | chr4 | 88492393 | |||||||
| chr4:88492573 | G | A | 4 | a0001c0001t0001g0152 a0001c0001t0001g0154 a0001c0001t0001g0167 others(1): Show |
4 | HG02280.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.2134-439G>A | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 16/22 | chr4 | 88492573 | |||||||
| chr4:88492660 | C | T | 2 | a0001c0001t0001g0039 a0001c0001t0001g0040 |
2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.2134-352C>T | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 16/22 | chr4 | 88492660 | |||||||
| chr4:88493411 | A | G | 1 | a0002c0002t0001g0200 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.2277+256A>G | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 17/22 | chr4 | 88493411 | |||||||
| chr4:88494374 | T | C | 2 | a0002c0002t0001g0012 a0002c0002t0001g0013 |
6 | HG00639.hp2 HG01109.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.2444+43T>C | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 18/22 | chr4 | 88494374 | |||||||
| chr4:88494400 | C | T | 1 | a0001c0001t0001g0158 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2444+69C>T | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 18/22 | chr4 | 88494400 | |||||||
| chr4:88494489 | G | A | 2 | a0002c0002t0001g0126 a0002c0002t0001g0182 |
2 | HG02698.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.2444+158G>A | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 18/22 | chr4 | 88494489 | |||||||
| chr4:88494536 | A | G | 13 | a0001c0001t0001g0009 a0001c0001t0001g0025 a0001c0001t0001g0026 others(10): Show |
17 | HG01167.hp2 HG01884.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.2444+205A>G | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 18/22 | chr4 | 88494536 | |||||||
| chr4:88494769 | G | A | 1 | a0001c0001t0001g0086 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2444+438G>A | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 18/22 | chr4 | 88494769 | |||||||
| chr4:88494934 | A | G | 1 | a0002c0002t0001g0191 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2444+603A>G | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 18/22 | chr4 | 88494934 | |||||||
| chr4:88495492 | C | T | 76 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(73): Show |
99 | HG00408.hp1 HG00544.hp2 HG00558.hp2 others(96): Show |
intron_variant | MODIFIER | c.2444+1161C>T | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 18/22 | chr4 | 88495492 | |||||||
| chr4:88495541 | C | T | 4 | a0001c0001t0001g0023 a0001c0001t0001g0136 a0001c0001t0001g0138 others(1): Show |
5 | HG02027.hp1 NA18999.hp1 NA19004.hp1 others(2): Show |
intron_variant | MODIFIER | c.2444+1210C>T | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 18/22 | chr4 | 88495541 | |||||||
| chr4:88495725 | T | G | 1 | a0001c0001t0001g0008 | 3 | HG01123.hp2 HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.2444+1394T>G | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 18/22 | chr4 | 88495725 | |||||||
| chr4:88496185 | G | T | 2 | a0002c0002t0001g0255 a0002c0002t0001g0256 |
2 | HG02886.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.2444+1854G>T | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 18/22 | chr4 | 88496185 | |||||||
| chr4:88496195 | T | G | 6 | a0001c0001t0001g0091 a0001c0001t0001g0097 a0001c0001t0001g0098 others(3): Show |
6 | HG00621.hp2 HG02015.hp2 HG02129.hp2 others(3): Show |
intron_variant | MODIFIER | c.2444+1864T>G | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 18/22 | chr4 | 88496195 | |||||||
| chr4:88496349 | A | C | 23 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0082 others(20): Show |
32 | HG00621.hp2 HG00642.hp2 HG00741.hp2 others(29): Show |
intron_variant | MODIFIER | c.2444+2018A>C | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 18/22 | chr4 | 88496349 | |||||||
| chr4:88496754 | A | T | 2 | a0001c0001t0001g0082 a0001c0001t0001g0093 |
2 | HG02056.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.2444+2423A>T | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 18/22 | chr4 | 88496754 | |||||||
| chr4:88496760 | G | T | 2 | a0001c0001t0001g0114 a0001c0001t0001g0134 |
2 | NA18954.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.2444+2429G>T | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 18/22 | chr4 | 88496760 | |||||||
| chr4:88496927 | T | C | 4 | a0001c0001t0001g0152 a0001c0001t0001g0154 a0001c0001t0001g0167 others(1): Show |
4 | HG02280.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.2444+2596T>C | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 18/22 | chr4 | 88496927 | |||||||
| chr4:88497518 | G | T | 1 | a0002c0002t0001g0205 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.2445-2408G>T | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 18/22 | chr4 | 88497518 | |||||||
| chr4:88497717 | G | A | 5 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(2): Show |
5 | HG02280.hp2 HG02615.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.2445-2209G>A | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 18/22 | chr4 | 88497717 | |||||||
| chr4:88497762 | A | C | 1 | a0001c0001t0001g0163 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2445-2164A>C | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 18/22 | chr4 | 88497762 | |||||||
| chr4:88498127 | G | T | 1 | a0001c0001t0001g0117 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.2445-1799G>T | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 18/22 | chr4 | 88498127 | |||||||
| chr4:88498198 | A | G | 1 | a0001c0004t0001g0017 | 2 | HG00140.hp2 HG00323.hp1 |
intron_variant | MODIFIER | c.2445-1728A>G | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 18/22 | chr4 | 88498198 | |||||||
| chr4:88498318 | G | T | 4 | a0001c0006t0001g0030 a0001c0006t0001g0070 a0001c0006t0001g0248 others(1): Show |
5 | HG02818.hp1 HG03516.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.2445-1608G>T | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 18/22 | chr4 | 88498318 | |||||||
| chr4:88498340 | C | T | 1 | a0001c0001t0001g0151 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2445-1586C>T | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 18/22 | chr4 | 88498340 | |||||||
| chr4:88498542 | A | G | 1 | a0002c0002t0001g0174 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.2445-1384A>G | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 18/22 | chr4 | 88498542 | |||||||
| chr4:88499388 | T | C | 45 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(42): Show |
55 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(52): Show |
intron_variant | MODIFIER | c.2445-538T>C | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 18/22 | chr4 | 88499388 | |||||||
| chr4:88499805 | G | T | 23 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0082 others(20): Show |
32 | HG00621.hp2 HG00642.hp2 HG00741.hp2 others(29): Show |
intron_variant | MODIFIER | c.2445-121G>T | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 18/22 | chr4 | 88499805 | |||||||
| chr4:88500089 | C | G | 1 | a0001c0001t0001g0114 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.2511+97C>G | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 19/22 | chr4 | 88500089 | |||||||
| chr4:88500356 | G | T | 1 | a0001c0001t0001g0135 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2511+364G>T | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 19/22 | chr4 | 88500356 | |||||||
| chr4:88500504 | A | G | 8 | a0001c0001t0001g0218 a0001c0001t0002g0014 a0001c0001t0002g0081 others(5): Show |
9 | HG01243.hp1 HG01884.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.2512-411A>G | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 19/22 | chr4 | 88500504 | |||||||
| chr4:88500515 | C | T | 2 | a0001c0001t0001g0152 a0001c0001t0001g0154 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.2512-400C>T | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 19/22 | chr4 | 88500515 | |||||||
| chr4:88501126 | T | C | 6 | a0002c0002t0001g0015 a0002c0002t0001g0029 a0002c0002t0001g0079 others(3): Show |
9 | HG02074.hp2 NA18945.hp2 NA18961.hp2 others(6): Show |
intron_variant | MODIFIER | c.2582+141T>C | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 20/22 | chr4 | 88501126 | |||||||
| chr4:88501246 | A | T | 1 | a0002c0002t0001g0210 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.2582+261A>T | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 20/22 | chr4 | 88501246 | |||||||
| chr4:88501590 | T | A | 4 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0074 others(1): Show |
4 | HG02615.hp1 HG03209.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.2582+605T>A | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 20/22 | chr4 | 88501590 | |||||||
| chr4:88501680 | A | T | 1 | a0001c0001t0001g0241 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.2582+695A>T | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 20/22 | chr4 | 88501680 | |||||||
| chr4:88501886 | C | T | 1 | a0001c0001t0001g0018 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.2582+901C>T | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 20/22 | chr4 | 88501886 | |||||||
| chr4:88501986 | G | GACGGTTT others(12): Show |
1 | a0001c0001t0001g0171 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2582+1003_2582+100 others(23): Show |
HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr4 | 88501986 | ||||||
| chr4:88501990 | G | C | 1 | a0001c0001t0001g0171 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2582+1005G>C | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 20/22 | chr4 | 88501990 | |||||||
| chr4:88501990 | G | GTAGAGTA others(3): Show |
1 | a0001c0001t0001g0163 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2582+1005_2582+100 others(14): Show |
HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 20/22 | chr4 | 88501990 | |||||||
| chr4:88502000 | G | A | 1 | a0002c0002t0001g0202 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2582+1015G>A | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 20/22 | chr4 | 88502000 | |||||||
| chr4:88502093 | C | T | 75 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(72): Show |
98 | HG00408.hp1 HG00544.hp2 HG00558.hp2 others(95): Show |
intron_variant | MODIFIER | c.2582+1108C>T | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 20/22 | chr4 | 88502093 | |||||||
| chr4:88502234 | T | C | 2 | a0001c0001t0001g0156 a0001c0001t0001g0160 |
2 | HG02258.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2582+1249T>C | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 20/22 | chr4 | 88502234 | |||||||
| chr4:88502283 | T | C | 1 | a0002c0002t0001g0220 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2582+1298T>C | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 20/22 | chr4 | 88502283 | |||||||
| chr4:88502577 | G | A | 19 | a0001c0001t0001g0009 a0001c0001t0001g0024 a0001c0001t0001g0025 others(16): Show |
23 | HG01167.hp2 HG01884.hp1 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.2582+1592G>A | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 20/22 | chr4 | 88502577 | |||||||
| chr4:88502598 | G | A | 2 | a0002c0002t0001g0031 a0002c0002t0001g0185 |
2 | HG00738.hp1 HG01123.hp1 |
intron_variant | MODIFIER | c.2582+1613G>A | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 20/22 | chr4 | 88502598 | |||||||
| chr4:88502649 | G | A | 2 | a0002c0002t0001g0187 a0002c0002t0001g0221 |
2 | HG03239.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.2583-1583G>A | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 20/22 | chr4 | 88502649 | |||||||
| chr4:88502776 | A | G | 1 | a0001c0001t0001g0218 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.2583-1456A>G | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 20/22 | chr4 | 88502776 | |||||||
| chr4:88502792 | A | G | 1 | a0001c0001t0001g0113 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.2583-1440A>G | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 20/22 | chr4 | 88502792 | |||||||
| chr4:88502800 | T | C | 1 | a0002c0002t0001g0177 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.2583-1432T>C | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 20/22 | chr4 | 88502800 | |||||||
| chr4:88502907 | CTT | C | 6 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0001g0139 others(3): Show |
6 | HG02109.hp2 HG02145.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.2583-1322_2583-132 others(6): Show |
HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr4 | 88502907 | ||||||
| chr4:88503329 | C | T | 1 | a0002c0002t0001g0201 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.2583-903C>T | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 20/22 | chr4 | 88503329 | |||||||
| chr4:88503591 | G | A | 2 | a0001c0001t0001g0053 a0001c0001t0001g0062 |
2 | HG00735.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.2583-641G>A | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 20/22 | chr4 | 88503591 | |||||||
| chr4:88503769 | A | G | 4 | a0002c0002t0001g0130 a0002c0002t0001g0200 a0002c0002t0001g0204 others(1): Show |
4 | NA18959.hp1 NA18962.hp1 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.2583-463A>G | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 20/22 | chr4 | 88503769 | |||||||
| chr4:88503870 | G | A | 1 | a0002c0002t0001g0203 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.2583-362G>A | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 20/22 | chr4 | 88503870 | |||||||
| chr4:88503926 | G | A | 1 | a0001c0001t0001g0122 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.2583-306G>A | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 20/22 | chr4 | 88503926 | |||||||
| chr4:88504045 | T | C | 1 | a0001c0001t0001g0025 | 2 | HG02622.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.2583-187T>C | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 20/22 | chr4 | 88504045 | |||||||
| chr4:88504051 | T | A | 1 | a0001c0001t0001g0025 | 2 | HG02622.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.2583-181T>A | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 20/22 | chr4 | 88504051 | |||||||
| chr4:88504066 | C | CAAAAAAA others(5): Show |
1 | a0001c0001t0001g0025 | 2 | HG02622.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.2583-162_2583-151d others(14): Show |
HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr4 | 88504066 | ||||||
| chr4:88504066 | CA | C | 16 | a0001c0001t0001g0009 a0001c0001t0001g0041 a0001c0001t0001g0072 others(13): Show |
18 | HG01167.hp2 HG01884.hp1 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.2583-151delA | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr4 | 88504066 | ||||||
| chr4:88504130 | G | A | 1 | a0002c0002t0001g0183 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.2583-102G>A | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 20/22 | chr4 | 88504130 | |||||||
| chr4:88504655 | A | T | 1 | a0001c0001t0001g0241 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.2869+58A>T | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 22/22 | chr4 | 88504655 | |||||||
| chr4:88505016 | A | G | 2 | a0002c0002t0001g0012 a0002c0002t0001g0013 |
6 | HG00639.hp2 HG01109.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.2869+419A>G | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 22/22 | chr4 | 88505016 | |||||||
| chr4:88505064 | A | AT | 4 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0074 others(1): Show |
4 | HG02615.hp1 HG03209.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.2869+468dupT | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr4 | 88505064 | ||||||
| chr4:88505230 | C | T | 2 | a0001c0001t0001g0018 a0001c0001t0001g0237 |
3 | HG02896.hp2 HG02897.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2870-443C>T | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 22/22 | chr4 | 88505230 | |||||||
| chr4:88505648 | T | G | 2 | a0001c0001t0001g0156 a0001c0001t0001g0160 |
2 | HG02258.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2870-25T>G | HERC5 | ENSG00000138646.9 | transcript | ENST00000264350.8 | protein_coding | 22/22 | chr4 | 88505648 |