Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 3067 |
| ensemblid | ENSG00000140287.11 |
| hgncid | 4855 |
| symbol | HDC |
| name | histidine decarboxylase |
| refseq_nuc | NM_002112.4 |
| refseq_prot | NP_002103.2 |
| ensembl_nuc | ENST00000267845.8 |
| ensembl_prot | ENSP00000267845.3 |
| mane_status | MANE Select |
| chr | chr15 |
| start | 50241947 |
| end | 50265726 |
| strand | - |
| ver | v1.2 |
| region | chr15:50241947-50265726 |
| region5000 | chr15:50236947-50270726 |
| regionname0 | HDC_chr15_50241947_50265726 |
| regionname5000 | HDC_chr15_50236947_50270726 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 662 | 362 | 78 | 64 | 155 | 16 | 47 | 120 | HDC_chr15_50236947_50270726 | HDC | MMEPE others(657): Show |
chr15 | 50236947 | 50270726 |
| a0002 | 0/0 | 662 | 30 | 10 | 4 | 14 | 2 | 0 | 9 | HDC_chr15_50236947_50270726 | HDC | MMEPE others(657): Show |
chr15 | 50236947 | 50270726 |
| a0003 | 0/0 | 662 | 18 | 0 | 8 | 9 | 0 | 1 | 5 | HDC_chr15_50236947_50270726 | HDC | MMEPE others(657): Show |
chr15 | 50236947 | 50270726 |
| a0004 | 0/0 | 662 | 7 | 6 | 1 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | MMEPE others(657): Show |
chr15 | 50236947 | 50270726 |
| a0005 | 0/0 | 662 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | MMEPE others(657): Show |
chr15 | 50236947 | 50270726 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1986 | 338 | 57 | 64 | 152 | 16 | 47 | HDC_chr15_50236947_50270726 | HDC | ATGAT others(1981): Show |
chr15 | 50236947 | 50270726 | ||
| a0001c0004 | 0/0 | 1986 | 10 | 10 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | ATGAT others(1981): Show |
chr15 | 50236947 | 50270726 | ||
| a0001c0005 | 0/0 | 1986 | 10 | 10 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | ATGAT others(1981): Show |
chr15 | 50236947 | 50270726 | ||
| a0001c0009 | 0/0 | 1986 | 2 | 0 | 0 | 2 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | ATGAT others(1981): Show |
chr15 | 50236947 | 50270726 | ||
| a0001c0010 | 0/0 | 1986 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | ATGAT others(1981): Show |
chr15 | 50236947 | 50270726 | ||
| a0001c0012 | 0/0 | 1986 | 1 | 1 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | ATGAT others(1981): Show |
chr15 | 50236947 | 50270726 | ||
| a0002c0002 | 0/0 | 1986 | 20 | 6 | 0 | 14 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | ATGAT others(1981): Show |
chr15 | 50236947 | 50270726 | ||
| a0002c0007 | 0/0 | 1986 | 7 | 1 | 4 | 0 | 2 | 0 | HDC_chr15_50236947_50270726 | HDC | ATGAT others(1981): Show |
chr15 | 50236947 | 50270726 | ||
| a0002c0008 | 0/0 | 1986 | 3 | 3 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | ATGAT others(1981): Show |
chr15 | 50236947 | 50270726 | ||
| a0003c0003 | 0/0 | 1986 | 18 | 0 | 8 | 9 | 0 | 1 | HDC_chr15_50236947_50270726 | HDC | ATGAT others(1981): Show |
chr15 | 50236947 | 50270726 | ||
| a0004c0006 | 0/0 | 1986 | 7 | 6 | 1 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | ATGAT others(1981): Show |
chr15 | 50236947 | 50270726 | ||
| a0005c0011 | 0/0 | 1986 | 1 | 0 | 1 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | ATGAT others(1981): Show |
chr15 | 50236947 | 50270726 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2405 | 336 | 57 | 62 | 152 | 16 | 47 | HDC_chr15_50236947_50270726 | HDC | GAGTG others(2400): Show |
chr15 | 50236947 | 50270726 |
| a0001c0001t0003 | 0/0 | 2405 | 2 | 0 | 2 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | GAGTG others(2400): Show |
chr15 | 50236947 | 50270726 |
| a0001c0004t0001 | 0/0 | 2405 | 10 | 10 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | GAGTG others(2400): Show |
chr15 | 50236947 | 50270726 |
| a0001c0005t0001 | 0/0 | 2405 | 6 | 6 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | GAGTG others(2400): Show |
chr15 | 50236947 | 50270726 |
| a0001c0005t0002 | 0/0 | 2405 | 4 | 4 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | GAGTG others(2400): Show |
chr15 | 50236947 | 50270726 |
| a0001c0009t0001 | 0/0 | 2405 | 2 | 0 | 0 | 2 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | GAGTG others(2400): Show |
chr15 | 50236947 | 50270726 |
| a0001c0010t0001 | 0/0 | 2405 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | GAGTG others(2400): Show |
chr15 | 50236947 | 50270726 |
| a0001c0012t0001 | 0/0 | 2405 | 1 | 1 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | GAGTG others(2400): Show |
chr15 | 50236947 | 50270726 |
| a0002c0002t0002 | 0/0 | 2405 | 20 | 6 | 0 | 14 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | GAGTG others(2400): Show |
chr15 | 50236947 | 50270726 |
| a0002c0007t0001 | 0/0 | 2405 | 7 | 1 | 4 | 0 | 2 | 0 | HDC_chr15_50236947_50270726 | HDC | GAGTG others(2400): Show |
chr15 | 50236947 | 50270726 |
| a0002c0008t0002 | 0/0 | 2405 | 3 | 3 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | GAGTG others(2400): Show |
chr15 | 50236947 | 50270726 |
| a0003c0003t0001 | 0/0 | 2405 | 18 | 0 | 8 | 9 | 0 | 1 | HDC_chr15_50236947_50270726 | HDC | GAGTG others(2400): Show |
chr15 | 50236947 | 50270726 |
| a0004c0006t0002 | 0/0 | 2405 | 7 | 6 | 1 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | GAGTG others(2400): Show |
chr15 | 50236947 | 50270726 |
| a0005c0011t0001 | 0/0 | 2405 | 1 | 0 | 1 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | GAGTG others(2400): Show |
chr15 | 50236947 | 50270726 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 44 | 14 | 8 | 13 | 4 | 5 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0002 | 0/0 | 22 | 0 | 2 | 19 | 0 | 1 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0003 | 0/0 | 18 | 1 | 1 | 13 | 1 | 2 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0004 | 0/0 | 14 | 0 | 5 | 3 | 1 | 5 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0005 | 0/0 | 13 | 0 | 2 | 6 | 2 | 3 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0006 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0007 | 0/0 | 7 | 0 | 5 | 0 | 2 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0008 | 0/0 | 7 | 5 | 2 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0009 | 0/0 | 6 | 0 | 0 | 3 | 0 | 3 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0012 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0014 | 0/0 | 4 | 2 | 2 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0015 | 0/0 | 4 | 1 | 0 | 3 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0016 | 0/0 | 4 | 2 | 1 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0017 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0018 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0019 | 0/0 | 4 | 1 | 2 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0024 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0025 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0026 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0027 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0031 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0037 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0043 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0047 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0048 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0049 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0076 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0094 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0003g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0001t0003g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0004t0001g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0004t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0004t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0004t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0004t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0004t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0004t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0004t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0004t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0005t0001g0011 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0005t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0005t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0005t0002g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0005t0002g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0005t0002g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0009t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0009t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0010t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0001c0012t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0002c0002t0002g0023 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0002c0002t0002g0028 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0002c0002t0002g0029 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0002c0002t0002g0030 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0002c0002t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0002c0002t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0002c0002t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0002c0002t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0002c0002t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0002c0002t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0002c0002t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0002c0002t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0002c0007t0001g0013 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0002c0007t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0002c0007t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0002c0007t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0002c0008t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0002c0008t0002g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0002c0008t0002g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0003c0003t0001g0010 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0003c0003t0001g0020 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0003c0003t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0003c0003t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0003c0003t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0003c0003t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0003c0003t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0003c0003t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0003c0003t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0003c0003t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0003c0003t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0004c0006t0002g0021 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0004c0006t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0004c0006t0002g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0004c0006t0002g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| a0005c0011t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0007 | t0001 | g0053 | EUR | GBR | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | GBR | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0037 | EUR | FIN | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0005 | EUR | FIN | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0203 | EUR | FIN | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG00408 | hp2 | a0002 | c0002 | t0002 | g0158 | EAS | CHS | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG00423 | hp2 | a0002 | c0002 | t0002 | g0028 | EAS | CHS | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | CHS | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | CHS | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG00558 | hp2 | a0003 | c0003 | t0001 | g0168 | EAS | CHS | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG00597 | hp1 | a0002 | c0002 | t0002 | g0165 | EAS | CHS | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG00609 | hp1 | a0003 | c0003 | t0001 | g0184 | EAS | CHS | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | CHS | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG00621 | hp2 | a0003 | c0003 | t0001 | g0167 | EAS | CHS | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | CHS | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG00733 | hp1 | a0002 | c0007 | t0001 | g0052 | AMR | PUR | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG00738 | hp1 | a0003 | c0003 | t0001 | g0010 | AMR | PUR | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG00741 | hp1 | a0003 | c0003 | t0001 | g0010 | AMR | PUR | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG01069 | hp2 | a0003 | c0003 | t0001 | g0183 | AMR | PUR | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG01070 | hp1 | a0003 | c0003 | t0001 | g0182 | AMR | PUR | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG01071 | hp1 | a0003 | c0003 | t0001 | g0010 | AMR | PUR | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG01074 | hp2 | a0002 | c0007 | t0001 | g0013 | AMR | PUR | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | PUR | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG01099 | hp2 | a0002 | c0007 | t0001 | g0013 | AMR | PUR | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG01106 | hp1 | a0003 | c0003 | t0001 | g0181 | AMR | PUR | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | PUR | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG01109 | hp2 | a0004 | c0006 | t0002 | g0172 | AMR | PUR | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG01168 | hp1 | a0005 | c0011 | t0001 | g0137 | AMR | PUR | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0205 | AMR | PUR | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | PUR | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0196 | AMR | PUR | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0194 | AMR | PUR | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG01243 | hp2 | a0003 | c0003 | t0001 | g0010 | AMR | PUR | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0208 | AMR | CLM | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | CLM | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0078 | AMR | CLM | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | CLM | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | CLM | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | CLM | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG01361 | hp1 | a0003 | c0003 | t0001 | g0010 | AMR | CLM | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG01496 | hp1 | a0001 | c0001 | t0003 | g0149 | AMR | CLM | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0007 | EUR | IBS | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0193 | EUR | IBS | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | IBS | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0043 | EUR | IBS | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0043 | EUR | IBS | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0007 | EUR | IBS | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | ACB | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | ACB | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG01891 | hp1 | a0001 | c0005 | t0002 | g0170 | AFR | ACB | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | ACB | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | PEL | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0190 | AMR | PEL | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PEL | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PEL | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG01975 | hp2 | a0001 | c0001 | t0003 | g0102 | AMR | PEL | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | PEL | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0197 | AMR | PEL | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | KHV | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | KHV | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG02027 | hp1 | a0002 | c0002 | t0002 | g0160 | EAS | KHV | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | KHV | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | KHV | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | KHV | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG02055 | hp1 | a0001 | c0004 | t0001 | g0180 | AFR | ACB | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG02055 | hp2 | a0002 | c0002 | t0002 | g0029 | AFR | ACB | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG02056 | hp1 | a0002 | c0002 | t0002 | g0166 | EAS | KHV | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG02056 | hp2 | a0001 | c0009 | t0001 | g0092 | EAS | KHV | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | KHV | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | KHV | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | KHV | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG02083 | hp2 | a0003 | c0003 | t0001 | g0020 | EAS | KHV | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | KHV | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | KHV | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG02145 | hp1 | a0004 | c0006 | t0002 | g0021 | AFR | ACB | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | CDX | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | CDX | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | ACB | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG02257 | hp2 | a0004 | c0006 | t0002 | g0021 | AFR | ACB | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG02258 | hp1 | a0001 | c0005 | t0001 | g0011 | AFR | ACB | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | ACB | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG02280 | hp2 | a0002 | c0002 | t0002 | g0029 | AFR | ACB | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0099 | AMR | PEL | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | PEL | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG02451 | hp1 | a0002 | c0002 | t0002 | g0023 | AFR | ACB | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG02451 | hp2 | a0001 | c0005 | t0002 | g0045 | AFR | ACB | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | KHV | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG02572 | hp1 | a0001 | c0005 | t0001 | g0050 | AFR | GWD | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG02572 | hp2 | a0001 | c0004 | t0001 | g0066 | AFR | GWD | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0144 | SAS | PJL | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0049 | SAS | PJL | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG02615 | hp2 | a0001 | c0005 | t0002 | g0177 | AFR | GWD | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG02622 | hp2 | a0004 | c0006 | t0002 | g0213 | AFR | GWD | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | GWD | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | GWD | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG02647 | hp2 | a0001 | c0005 | t0001 | g0011 | AFR | GWD | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0034 | SAS | PJL | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0069 | SAS | PJL | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG02717 | hp1 | a0001 | c0005 | t0001 | g0133 | AFR | GWD | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0097 | SAS | PJL | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0195 | SAS | PJL | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0140 | SAS | PJL | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0207 | SAS | PJL | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG02809 | hp1 | a0001 | c0005 | t0001 | g0011 | AFR | GWD | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG02818 | hp2 | a0001 | c0004 | t0001 | g0128 | AFR | GWD | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG02886 | hp2 | a0004 | c0006 | t0002 | g0021 | AFR | GWD | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG02896 | hp2 | a0001 | c0004 | t0001 | g0125 | AFR | GWD | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG02922 | hp1 | a0002 | c0008 | t0002 | g0189 | AFR | ESN | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | ESN | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | ESN | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ESN | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG02970 | hp1 | a0002 | c0002 | t0002 | g0023 | AFR | ESN | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG02970 | hp2 | a0001 | c0004 | t0001 | g0178 | AFR | ESN | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG02976 | hp1 | a0001 | c0005 | t0001 | g0011 | AFR | ESN | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0188 | AFR | ESN | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0202 | SAS | PJL | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | GWD | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | GWD | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG03098 | hp2 | a0001 | c0004 | t0001 | g0129 | AFR | MSL | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG03130 | hp2 | a0001 | c0004 | t0001 | g0046 | AFR | ESN | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | ESN | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG03195 | hp2 | a0001 | c0012 | t0001 | g0126 | AFR | ESN | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG03209 | hp1 | a0004 | c0006 | t0002 | g0021 | AFR | MSL | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG03209 | hp2 | a0001 | c0004 | t0001 | g0127 | AFR | MSL | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | MSL | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG03225 | hp2 | a0002 | c0008 | t0002 | g0210 | AFR | MSL | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0048 | SAS | PJL | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0199 | SAS | PJL | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | MSL | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | MSL | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | MSL | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0039 | SAS | PJL | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0198 | SAS | PJL | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0141 | SAS | PJL | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0034 | SAS | PJL | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0039 | SAS | PJL | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0041 | SAS | PJL | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | ESN | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0176 | AFR | ESN | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | MSL | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0150 | SAS | STU | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0061 | SAS | STU | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0071 | SAS | PJL | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0114 | SAS | BEB | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | BEB | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0048 | SAS | BEB | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0049 | SAS | BEB | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | BEB | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0042 | SAS | BEB | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | STU | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | BEB | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG04199 | hp1 | a0003 | c0003 | t0001 | g0185 | SAS | STU | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0101 | SAS | STU | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0135 | SAS | STU | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0109 | SAS | STU | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | YRI | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | CHB | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | CHB | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | YRI | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | YRI | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA18941 | hp1 | a0002 | c0002 | t0002 | g0159 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA18949 | hp2 | a0002 | c0002 | t0002 | g0028 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA18974 | hp2 | a0001 | c0010 | t0001 | g0124 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA18975 | hp2 | a0002 | c0002 | t0002 | g0164 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA18980 | hp2 | a0002 | c0002 | t0002 | g0030 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA18981 | hp2 | a0002 | c0002 | t0002 | g0030 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA19000 | hp1 | a0003 | c0003 | t0001 | g0169 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA19001 | hp1 | a0003 | c0003 | t0001 | g0020 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA19005 | hp2 | a0002 | c0002 | t0002 | g0028 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA19007 | hp1 | a0003 | c0003 | t0001 | g0020 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | LWK | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | LWK | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | LWK | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | LWK | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA19067 | hp1 | a0003 | c0003 | t0001 | g0186 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA19067 | hp2 | a0002 | c0002 | t0002 | g0179 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA19077 | hp1 | a0001 | c0009 | t0001 | g0113 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA19089 | hp1 | a0002 | c0002 | t0002 | g0030 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA19090 | hp1 | a0003 | c0003 | t0001 | g0020 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA19091 | hp1 | a0002 | c0002 | t0002 | g0087 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA19240 | hp1 | a0002 | c0002 | t0002 | g0029 | AFR | YRI | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA19240 | hp2 | a0002 | c0002 | t0002 | g0023 | AFR | YRI | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ASW | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA20129 | hp2 | a0001 | c0004 | t0001 | g0046 | AFR | ASW | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA20752 | hp2 | a0002 | c0007 | t0001 | g0013 | EUR | TSI | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0106 | EUR | TSI | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0005 | EUR | TSI | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0200 | SAS | GIH | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG01123 | hp2 | a0002 | c0007 | t0001 | g0013 | AMR | CLM | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | ACB | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0204 | AFR | ACB | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG02486 | hp1 | a0002 | c0007 | t0001 | g0212 | AFR | ACB | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0209 | AFR | ACB | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0206 | AFR | ACB | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG03471 | hp1 | a0001 | c0005 | t0002 | g0045 | AFR | MSL | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG03471 | hp2 | a0002 | c0008 | t0002 | g0130 | AFR | MSL | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG06807 | hp1 | a0004 | c0006 | t0002 | g0131 | AFR | USA | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | USA | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | USA | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| NA20300 | hp2 | a0001 | c0004 | t0001 | g0142 | AFR | USA | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0076 | REF | REF | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0094 | REF | REF | HDC_chr15_50236947_50270726 | HDC | chr15 | 50236947 | 50270726 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:50242317 | T | G | 2 | a0002 a0004 |
37 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(34): Show |
missense_variant | MODERATE | c.1932A>C | p.Glu644Asp | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 12/12 | 2035/2405 | 1932/1989 | 644/662 | chr15 | 50242317 | |||
| chr15:50242592 | A | G | 1 | a0004 | 7 | HG01109.hp2 HG02145.hp1 HG02257.hp2 others(4): Show |
missense_variant | MODERATE | c.1657T>C | p.Phe553Leu | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 12/12 | 1760/2405 | 1657/1989 | 553/662 | chr15 | 50242592 | |||
| chr15:50242769 | T | C | 1 | a0005 | 1 | HG01168.hp1 | missense_variant | MODERATE | c.1480A>G | p.Ile494Val | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 12/12 | 1583/2405 | 1480/1989 | 494/662 | chr15 | 50242769 | |||
| chr15:50263347 | G | A | 1 | a0003 | 18 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(15): Show |
missense_variant | MODERATE | c.92C>T | p.Thr31Met | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/12 | 195/2405 | 92/1989 | 31/662 | chr15 | 50263347 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:50242479 | C | T | 1 | a0001c0004 | 10 | HG02055.hp1 HG02572.hp2 HG02818.hp2 others(7): Show |
synonymous_variant | LOW | c.1770G>A | p.Val590Val | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 12/12 | 1873/2405 | 1770/1989 | 590/662 | chr15 | 50242479 | |||
| chr15:50242506 | C | T | 1 | a0002c0002 | 20 | HG00408.hp2 HG00423.hp2 HG00597.hp1 others(17): Show |
synonymous_variant | LOW | c.1743G>A | p.Thr581Thr | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 12/12 | 1846/2405 | 1743/1989 | 581/662 | chr15 | 50242506 | |||
| chr15:50242635 | A | G | 6 | a0001c0004 a0001c0005 a0002c0002 others(3): Show |
57 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(54): Show |
synonymous_variant | LOW | c.1614T>C | p.Asn538Asn | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 12/12 | 1717/2405 | 1614/1989 | 538/662 | chr15 | 50242635 | |||
| chr15:50242842 | A | G | 1 | a0001c0009 | 2 | HG02056.hp2 NA19077.hp1 |
synonymous_variant | LOW | c.1407T>C | p.Asp469Asp | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 12/12 | 1510/2405 | 1407/1989 | 469/662 | chr15 | 50242842 | |||
| chr15:50252674 | G | A | 1 | a0002c0007 | 7 | HG00099.hp1 HG00733.hp1 HG01074.hp2 others(4): Show |
synonymous_variant | LOW | c.888C>T | p.Ala296Ala | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 8/12 | 991/2405 | 888/1989 | 296/662 | chr15 | 50252674 | |||
| chr15:50254545 | G | A | 1 | a0001c0012 | 1 | HG03195.hp2 | synonymous_variant | LOW | c.561C>T | p.Ala187Ala | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 5/12 | 664/2405 | 561/1989 | 187/662 | chr15 | 50254545 | |||
| chr15:50263331 | A | T | 1 | a0001c0010 | 1 | NA18974.hp2 | synonymous_variant | LOW | c.108T>A | p.Pro36Pro | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/12 | 211/2405 | 108/1989 | 36/662 | chr15 | 50263331 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:50242182 | A | G | 1 | a0001c0001t0003 | 2 | HG01496.hp1 HG01975.hp2 |
3_prime_UTR_variant | MODIFIER | c.*78T>C | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 12/12 | 78 | chr15 | 50242182 | ||||||
| chr15:50242257 | T | G | 4 | a0001c0005t0002 a0002c0002t0002 a0002c0008t0002 others(1): Show |
34 | HG00408.hp2 HG00423.hp2 HG00597.hp1 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*3A>C | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 12/12 | 3 | chr15 | 50242257 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:50243061 | C | A | 1 | a0001c0005t0002g0177 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1243-55G>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 11/11 | chr15 | 50243061 | |||||||
| chr15:50243431 | C | T | 12 | a0002c0002t0002g0023 a0002c0002t0002g0028 a0002c0002t0002g0029 others(9): Show |
20 | HG00408.hp2 HG00423.hp2 HG00597.hp1 others(17): Show |
intron_variant | MODIFIER | c.1141-187G>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 10/11 | chr15 | 50243431 | |||||||
| chr15:50243514 | A | G | 2 | a0002c0002t0002g0030 a0002c0002t0002g0159 |
4 | NA18941.hp1 NA18980.hp2 NA18981.hp2 others(1): Show |
intron_variant | MODIFIER | c.1141-270T>C | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 10/11 | chr15 | 50243514 | |||||||
| chr15:50243539 | G | A | 1 | a0002c0008t0002g0210 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1141-295C>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 10/11 | chr15 | 50243539 | |||||||
| chr15:50243547 | C | T | 1 | a0001c0001t0001g0101 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1141-303G>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 10/11 | chr15 | 50243547 | |||||||
| chr15:50243610 | C | A | 1 | a0001c0001t0001g0199 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1141-366G>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 10/11 | chr15 | 50243610 | |||||||
| chr15:50243615 | C | T | 18 | a0002c0002t0002g0023 a0002c0002t0002g0028 a0002c0002t0002g0029 others(15): Show |
29 | HG00408.hp2 HG00423.hp2 HG00597.hp1 others(26): Show |
intron_variant | MODIFIER | c.1141-371G>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 10/11 | chr15 | 50243615 | |||||||
| chr15:50243616 | G | A | 2 | a0001c0004t0001g0142 a0001c0004t0001g0180 |
2 | HG02055.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1141-372C>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 10/11 | chr15 | 50243616 | |||||||
| chr15:50243677 | G | A | 3 | a0001c0005t0002g0045 a0001c0005t0002g0170 a0001c0005t0002g0177 |
4 | HG01891.hp1 HG02451.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.1141-433C>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 10/11 | chr15 | 50243677 | |||||||
| chr15:50243707 | G | A | 18 | a0002c0002t0002g0023 a0002c0002t0002g0028 a0002c0002t0002g0029 others(15): Show |
29 | HG00408.hp2 HG00423.hp2 HG00597.hp1 others(26): Show |
intron_variant | MODIFIER | c.1141-463C>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 10/11 | chr15 | 50243707 | |||||||
| chr15:50243744 | G | A | 1 | a0002c0002t0002g0087 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1141-500C>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 10/11 | chr15 | 50243744 | |||||||
| chr15:50243871 | T | C | 1 | a0001c0001t0001g0148 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.1141-627A>G | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 10/11 | chr15 | 50243871 | |||||||
| chr15:50244031 | T | C | 1 | a0001c0001t0001g0161 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1141-787A>G | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 10/11 | chr15 | 50244031 | |||||||
| chr15:50244155 | C | T | 21 | a0001c0005t0002g0045 a0001c0005t0002g0170 a0001c0005t0002g0177 others(18): Show |
33 | HG00408.hp2 HG00423.hp2 HG00597.hp1 others(30): Show |
intron_variant | MODIFIER | c.1141-911G>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 10/11 | chr15 | 50244155 | |||||||
| chr15:50244161 | T | C | 1 | a0001c0001t0001g0077 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1141-917A>G | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 10/11 | chr15 | 50244161 | |||||||
| chr15:50244241 | T | C | 21 | a0001c0005t0002g0045 a0001c0005t0002g0170 a0001c0005t0002g0177 others(18): Show |
33 | HG00408.hp2 HG00423.hp2 HG00597.hp1 others(30): Show |
intron_variant | MODIFIER | c.1141-997A>G | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 10/11 | chr15 | 50244241 | |||||||
| chr15:50244283 | C | G | 1 | a0001c0001t0001g0136 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1141-1039G>C | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 10/11 | chr15 | 50244283 | |||||||
| chr15:50244285 | C | CT | 19 | a0001c0001t0001g0015 a0001c0001t0001g0038 a0001c0001t0001g0040 others(16): Show |
25 | HG00642.hp1 HG00673.hp2 HG01981.hp1 others(22): Show |
intron_variant | MODIFIER | c.1141-1042dupA | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 10/11 | chr15 | 50244285 | |||||||
| chr15:50244285 | CT | C | 30 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0018 others(27): Show |
49 | HG00323.hp1 HG00738.hp2 HG01069.hp1 others(46): Show |
intron_variant | MODIFIER | c.1141-1042delA | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 10/11 | chr15 | 50244285 | |||||||
| chr15:50244285 | CTTT | C | 4 | a0001c0005t0001g0133 a0002c0007t0001g0013 a0002c0007t0001g0052 others(1): Show |
7 | HG00733.hp1 HG01074.hp2 HG01099.hp2 others(4): Show |
intron_variant | MODIFIER | c.1141-1044_1141-104 others(7): Show |
HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 10/11 | chr15 | 50244285 | |||||||
| chr15:50244285 | CTTTT | C | 19 | a0002c0002t0002g0023 a0002c0002t0002g0028 a0002c0002t0002g0029 others(16): Show |
30 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(27): Show |
intron_variant | MODIFIER | c.1141-1045_1141-104 others(8): Show |
HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 10/11 | chr15 | 50244285 | |||||||
| chr15:50244285 | CTTTTTTT others(5): Show |
C | 7 | a0001c0004t0001g0046 a0001c0004t0001g0066 a0001c0004t0001g0125 others(4): Show |
8 | HG02572.hp2 HG02818.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1141-1053_1141-104 others(16): Show |
HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 10/11 | chr15 | 50244285 | |||||||
| chr15:50244298 | T | G | 18 | a0002c0002t0002g0023 a0002c0002t0002g0028 a0002c0002t0002g0029 others(15): Show |
29 | HG00408.hp2 HG00423.hp2 HG00597.hp1 others(26): Show |
intron_variant | MODIFIER | c.1141-1054A>C | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 10/11 | chr15 | 50244298 | |||||||
| chr15:50244312 | G | T | 1 | a0001c0005t0002g0170 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1141-1068C>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 10/11 | chr15 | 50244312 | |||||||
| chr15:50244313 | A | T | 1 | a0001c0005t0002g0170 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1141-1069T>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 10/11 | chr15 | 50244313 | |||||||
| chr15:50244318 | T | G | 1 | a0001c0001t0001g0089 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1141-1074A>C | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 10/11 | chr15 | 50244318 | |||||||
| chr15:50244385 | C | G | 1 | a0001c0004t0001g0125 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1141-1141G>C | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 10/11 | chr15 | 50244385 | |||||||
| chr15:50244415 | A | ACCTTCAC others(1): Show |
21 | a0001c0005t0002g0045 a0001c0005t0002g0170 a0001c0005t0002g0177 others(18): Show |
33 | HG00408.hp2 HG00423.hp2 HG00597.hp1 others(30): Show |
intron_variant | MODIFIER | c.1141-1179_1141-117 others(12): Show |
HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 10/11 | chr15 | 50244415 | |||||||
| chr15:50244422 | C | T | 1 | a0001c0001t0001g0024 | 3 | HG00609.hp2 NA18957.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.1141-1178G>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 10/11 | chr15 | 50244422 | |||||||
| chr15:50244615 | T | C | 1 | a0001c0001t0001g0034 | 2 | HG02683.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.1141-1371A>G | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 10/11 | chr15 | 50244615 | |||||||
| chr15:50244646 | A | T | 9 | a0001c0001t0001g0043 a0001c0001t0001g0099 a0003c0003t0001g0010 others(6): Show |
14 | HG00609.hp1 HG00738.hp1 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.1141-1402T>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 10/11 | chr15 | 50244646 | |||||||
| chr15:50244678 | G | C | 1 | a0001c0009t0001g0113 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1141-1434C>G | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 10/11 | chr15 | 50244678 | |||||||
| chr15:50244985 | C | T | 21 | a0001c0005t0002g0045 a0001c0005t0002g0170 a0001c0005t0002g0177 others(18): Show |
33 | HG00408.hp2 HG00423.hp2 HG00597.hp1 others(30): Show |
intron_variant | MODIFIER | c.1141-1741G>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 10/11 | chr15 | 50244985 | |||||||
| chr15:50245281 | C | G | 1 | a0003c0003t0001g0020 | 4 | HG02083.hp2 NA19001.hp1 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.1141-2037G>C | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 10/11 | chr15 | 50245281 | |||||||
| chr15:50245281 | C | T | 21 | a0001c0005t0002g0045 a0001c0005t0002g0170 a0001c0005t0002g0177 others(18): Show |
33 | HG00408.hp2 HG00423.hp2 HG00597.hp1 others(30): Show |
intron_variant | MODIFIER | c.1141-2037G>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 10/11 | chr15 | 50245281 | |||||||
| chr15:50245323 | G | A | 1 | a0001c0001t0001g0085 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1141-2079C>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 10/11 | chr15 | 50245323 | |||||||
| chr15:50245352 | C | T | 25 | a0001c0005t0002g0045 a0001c0005t0002g0170 a0001c0005t0002g0177 others(22): Show |
40 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(37): Show |
intron_variant | MODIFIER | c.1141-2108G>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 10/11 | chr15 | 50245352 | |||||||
| chr15:50245357 | AATGTTTA others(26): Show |
A | 1 | a0001c0001t0001g0027 | 3 | NA18957.hp2 NA18982.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.1141-2146_1141-211 others(37): Show |
HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 10/11 | chr15 | 50245357 | |||||||
| chr15:50245415 | G | A | 1 | a0001c0001t0001g0176 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1141-2171C>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 10/11 | chr15 | 50245415 | |||||||
| chr15:50245646 | G | A | 2 | a0001c0001t0003g0102 a0001c0001t0003g0149 |
2 | HG01496.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.1141-2402C>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 10/11 | chr15 | 50245646 | |||||||
| chr15:50245691 | G | T | 37 | a0001c0001t0001g0157 a0001c0004t0001g0046 a0001c0004t0001g0066 others(34): Show |
53 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(50): Show |
intron_variant | MODIFIER | c.1141-2447C>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 10/11 | chr15 | 50245691 | |||||||
| chr15:50245765 | T | G | 1 | a0004c0006t0002g0172 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1140+2480A>C | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 10/11 | chr15 | 50245765 | |||||||
| chr15:50245768 | G | A | 10 | a0001c0001t0001g0007 a0001c0001t0001g0039 a0001c0001t0001g0041 others(7): Show |
18 | HG00642.hp1 HG01081.hp1 HG01168.hp1 others(15): Show |
intron_variant | MODIFIER | c.1140+2477C>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 10/11 | chr15 | 50245768 | |||||||
| chr15:50245904 | C | CAATA | 39 | a0001c0001t0001g0157 a0001c0004t0001g0046 a0001c0004t0001g0066 others(36): Show |
58 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(55): Show |
intron_variant | MODIFIER | c.1140+2337_1140+234 others(8): Show |
HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 10/11 | chr15 | 50245904 | |||||||
| chr15:50246127 | G | A | 1 | a0001c0001t0001g0150 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1140+2118C>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 10/11 | chr15 | 50246127 | |||||||
| chr15:50246183 | T | C | 1 | a0001c0001t0001g0151 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1140+2062A>G | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 10/11 | chr15 | 50246183 | |||||||
| chr15:50246189 | C | T | 2 | a0003c0003t0001g0182 a0003c0003t0001g0184 |
2 | HG00609.hp1 HG01070.hp1 |
intron_variant | MODIFIER | c.1140+2056G>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 10/11 | chr15 | 50246189 | |||||||
| chr15:50246252 | C | T | 7 | a0001c0004t0001g0046 a0001c0004t0001g0127 a0001c0004t0001g0129 others(4): Show |
8 | HG02055.hp1 HG02717.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.1140+1993G>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 10/11 | chr15 | 50246252 | |||||||
| chr15:50246253 | G | A | 1 | a0001c0001t0001g0176 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1140+1992C>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 10/11 | chr15 | 50246253 | |||||||
| chr15:50246478 | T | G | 1 | a0001c0004t0001g0180 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1140+1767A>C | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 10/11 | chr15 | 50246478 | |||||||
| chr15:50246533 | C | T | 2 | a0002c0002t0002g0087 a0002c0002t0002g0160 |
2 | HG02027.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.1140+1712G>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 10/11 | chr15 | 50246533 | |||||||
| chr15:50246655 | G | T | 10 | a0001c0001t0001g0173 a0001c0001t0001g0174 a0001c0001t0001g0175 others(7): Show |
13 | HG01891.hp2 HG02145.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.1140+1590C>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 10/11 | chr15 | 50246655 | |||||||
| chr15:50246872 | G | A | 2 | a0001c0001t0001g0103 a0001c0001t0001g0115 |
2 | NA19000.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.1140+1373C>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 10/11 | chr15 | 50246872 | |||||||
| chr15:50246904 | G | A | 3 | a0001c0004t0001g0046 a0001c0004t0001g0178 a0001c0005t0002g0177 |
4 | HG02615.hp2 HG02970.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1140+1341C>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 10/11 | chr15 | 50246904 | |||||||
| chr15:50246919 | G | A | 1 | a0001c0001t0001g0176 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1140+1326C>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 10/11 | chr15 | 50246919 | |||||||
| chr15:50247023 | C | T | 1 | a0001c0001t0001g0067 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1140+1222G>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 10/11 | chr15 | 50247023 | |||||||
| chr15:50247062 | C | T | 1 | a0001c0001t0001g0036 | 2 | NA18953.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.1140+1183G>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 10/11 | chr15 | 50247062 | |||||||
| chr15:50247195 | T | C | 2 | a0001c0005t0002g0045 a0001c0005t0002g0170 |
3 | HG01891.hp1 HG02451.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1140+1050A>G | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 10/11 | chr15 | 50247195 | |||||||
| chr15:50247199 | C | T | 10 | a0001c0001t0001g0143 a0001c0005t0002g0045 a0001c0005t0002g0170 others(7): Show |
14 | HG01109.hp2 HG01891.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.1140+1046G>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 10/11 | chr15 | 50247199 | |||||||
| chr15:50247271 | A | G | 21 | a0001c0001t0001g0173 a0001c0001t0001g0174 a0001c0001t0001g0175 others(18): Show |
28 | HG00099.hp1 HG00733.hp1 HG01074.hp2 others(25): Show |
intron_variant | MODIFIER | c.1140+974T>C | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 10/11 | chr15 | 50247271 | |||||||
| chr15:50247364 | C | T | 10 | a0001c0001t0001g0043 a0001c0001t0001g0099 a0001c0001t0001g0146 others(7): Show |
15 | HG00609.hp1 HG00738.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.1140+881G>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 10/11 | chr15 | 50247364 | |||||||
| chr15:50247365 | G | A | 1 | a0001c0001t0001g0152 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1140+880C>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 10/11 | chr15 | 50247365 | |||||||
| chr15:50247399 | T | A | 1 | a0001c0001t0001g0090 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1140+846A>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 10/11 | chr15 | 50247399 | |||||||
| chr15:50247952 | CTT | C | 26 | a0001c0001t0001g0099 a0001c0001t0001g0139 a0001c0004t0001g0046 others(23): Show |
37 | HG00099.hp1 HG00609.hp1 HG00733.hp1 others(34): Show |
intron_variant | MODIFIER | c.1140+291_1140+292d others(4): Show |
HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 10/11 | chr15 | 50247952 | |||||||
| chr15:50248145 | G | T | 4 | a0001c0001t0001g0173 a0001c0001t0001g0174 a0001c0001t0001g0175 others(1): Show |
4 | HG01891.hp2 HG03041.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1140+100C>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 10/11 | chr15 | 50248145 | |||||||
| chr15:50248504 | G | A | 1 | a0001c0005t0001g0133 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1042-161C>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 9/11 | chr15 | 50248504 | |||||||
| chr15:50248700 | T | A | 197 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(194): Show |
395 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(392): Show |
intron_variant | MODIFIER | c.1042-357A>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 9/11 | chr15 | 50248700 | |||||||
| chr15:50248774 | A | G | 1 | a0001c0001t0001g0145 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1042-431T>C | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 9/11 | chr15 | 50248774 | |||||||
| chr15:50248898 | C | T | 1 | a0001c0001t0001g0108 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1042-555G>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 9/11 | chr15 | 50248898 | |||||||
| chr15:50249135 | G | A | 1 | a0001c0001t0001g0032 | 2 | NA18948.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.1042-792C>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 9/11 | chr15 | 50249135 | |||||||
| chr15:50249396 | C | T | 1 | a0001c0001t0001g0121 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1042-1053G>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 9/11 | chr15 | 50249396 | |||||||
| chr15:50249600 | A | T | 1 | a0001c0001t0001g0059 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1042-1257T>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 9/11 | chr15 | 50249600 | |||||||
| chr15:50249663 | A | C | 1 | a0001c0001t0001g0134 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1042-1320T>G | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 9/11 | chr15 | 50249663 | |||||||
| chr15:50249681 | A | G | 3 | a0001c0001t0001g0025 a0001c0001t0001g0080 a0001c0001t0001g0081 |
5 | HG01884.hp1 HG02630.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1042-1338T>C | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 9/11 | chr15 | 50249681 | |||||||
| chr15:50249800 | A | C | 1 | a0002c0002t0002g0023 | 3 | HG02451.hp1 HG02970.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1042-1457T>G | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 9/11 | chr15 | 50249800 | |||||||
| chr15:50249953 | C | T | 3 | a0001c0004t0001g0046 a0001c0004t0001g0178 a0001c0005t0002g0177 |
4 | HG02615.hp2 HG02970.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1042-1610G>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 9/11 | chr15 | 50249953 | |||||||
| chr15:50249962 | C | G | 61 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0018 others(58): Show |
115 | HG00438.hp1 HG00544.hp2 HG00558.hp1 others(112): Show |
intron_variant | MODIFIER | c.1042-1619G>C | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 9/11 | chr15 | 50249962 | |||||||
| chr15:50250056 | G | A | 3 | a0001c0001t0001g0068 a0001c0001t0001g0104 a0001c0001t0001g0123 |
3 | NA18959.hp2 NA18967.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.1042-1713C>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 9/11 | chr15 | 50250056 | |||||||
| chr15:50250173 | A | G | 1 | a0001c0001t0001g0196 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1042-1830T>C | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 9/11 | chr15 | 50250173 | |||||||
| chr15:50250349 | T | C | 1 | a0001c0001t0001g0109 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1042-2006A>G | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 9/11 | chr15 | 50250349 | |||||||
| chr15:50250419 | G | A | 1 | a0001c0001t0001g0144 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1041+2011C>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 9/11 | chr15 | 50250419 | |||||||
| chr15:50250442 | C | T | 1 | a0001c0005t0001g0133 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1041+1988G>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 9/11 | chr15 | 50250442 | |||||||
| chr15:50250486 | G | A | 1 | a0001c0001t0001g0105 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1041+1944C>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 9/11 | chr15 | 50250486 | |||||||
| chr15:50250522 | A | G | 54 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0018 others(51): Show |
104 | HG00438.hp1 HG00544.hp2 HG00558.hp1 others(101): Show |
intron_variant | MODIFIER | c.1041+1908T>C | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 9/11 | chr15 | 50250522 | |||||||
| chr15:50250569 | T | A | 1 | a0001c0001t0001g0027 | 3 | NA18957.hp2 NA18982.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.1041+1861A>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 9/11 | chr15 | 50250569 | |||||||
| chr15:50251056 | C | T | 9 | a0001c0004t0001g0066 a0001c0004t0001g0125 a0001c0004t0001g0127 others(6): Show |
12 | HG00099.hp1 HG00733.hp1 HG01074.hp2 others(9): Show |
intron_variant | MODIFIER | c.1041+1374G>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 9/11 | chr15 | 50251056 | |||||||
| chr15:50251311 | T | C | 1 | a0001c0001t0001g0201 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1041+1119A>G | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 9/11 | chr15 | 50251311 | |||||||
| chr15:50251326 | G | C | 1 | a0001c0001t0001g0069 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1041+1104C>G | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 9/11 | chr15 | 50251326 | |||||||
| chr15:50251342 | G | A | 3 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0176 |
3 | HG01891.hp2 HG03486.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1041+1088C>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 9/11 | chr15 | 50251342 | |||||||
| chr15:50251365 | C | T | 1 | a0003c0003t0001g0181 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1041+1065G>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 9/11 | chr15 | 50251365 | |||||||
| chr15:50251528 | C | G | 1 | a0001c0001t0001g0065 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1041+902G>C | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 9/11 | chr15 | 50251528 | |||||||
| chr15:50251692 | C | T | 1 | a0004c0006t0002g0131 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1041+738G>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 9/11 | chr15 | 50251692 | |||||||
| chr15:50251693 | G | A | 1 | a0001c0001t0001g0139 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1041+737C>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 9/11 | chr15 | 50251693 | |||||||
| chr15:50251694 | C | T | 23 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0019 others(20): Show |
45 | HG00280.hp2 HG00423.hp1 HG00673.hp2 others(42): Show |
intron_variant | MODIFIER | c.1041+736G>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 9/11 | chr15 | 50251694 | |||||||
| chr15:50251704 | C | G | 1 | a0001c0004t0001g0125 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1041+726G>C | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 9/11 | chr15 | 50251704 | |||||||
| chr15:50251722 | C | T | 7 | a0001c0001t0001g0038 a0001c0001t0001g0040 a0001c0001t0001g0042 others(4): Show |
10 | HG03942.hp2 NA18954.hp1 NA18960.hp2 others(7): Show |
intron_variant | MODIFIER | c.1041+708G>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 9/11 | chr15 | 50251722 | |||||||
| chr15:50251742 | G | C | 1 | a0001c0001t0001g0070 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1041+688C>G | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 9/11 | chr15 | 50251742 | |||||||
| chr15:50251819 | G | A | 1 | a0001c0001t0001g0176 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1041+611C>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 9/11 | chr15 | 50251819 | |||||||
| chr15:50251831 | C | CA | 33 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0019 others(30): Show |
61 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(58): Show |
intron_variant | MODIFIER | c.1041+598dupT | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 9/11 | chr15 | 50251831 | |||||||
| chr15:50251833 | G | A | 117 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(114): Show |
214 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(211): Show |
intron_variant | MODIFIER | c.1041+597C>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 9/11 | chr15 | 50251833 | |||||||
| chr15:50251841 | A | G | 1 | a0001c0001t0001g0203 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1041+589T>C | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 9/11 | chr15 | 50251841 | |||||||
| chr15:50251845 | G | A | 2 | a0001c0005t0002g0045 a0001c0005t0002g0170 |
3 | HG01891.hp1 HG02451.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1041+585C>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 9/11 | chr15 | 50251845 | |||||||
| chr15:50251874 | AAG | A | 6 | a0001c0001t0001g0139 a0001c0001t0001g0174 a0001c0001t0001g0175 others(3): Show |
6 | HG01167.hp2 HG01891.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.1041+554_1041+555d others(4): Show |
HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 9/11 | chr15 | 50251874 | |||||||
| chr15:50251933 | T | C | 8 | a0001c0004t0001g0125 a0001c0004t0001g0127 a0001c0004t0001g0128 others(5): Show |
11 | HG00099.hp1 HG00733.hp1 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.1041+497A>G | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 9/11 | chr15 | 50251933 | |||||||
| chr15:50252012 | C | CA | 11 | a0001c0001t0001g0008 a0001c0001t0001g0096 a0001c0001t0001g0171 others(8): Show |
18 | HG00323.hp1 HG00639.hp2 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.1041+417dupT | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 9/11 | chr15 | 50252012 | |||||||
| chr15:50252043 | C | T | 6 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0176 others(3): Show |
6 | HG01891.hp2 HG02055.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.1041+387G>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 9/11 | chr15 | 50252043 | |||||||
| chr15:50252110 | G | C | 2 | a0001c0005t0002g0045 a0001c0005t0002g0170 |
3 | HG01891.hp1 HG02451.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1041+320C>G | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 9/11 | chr15 | 50252110 | |||||||
| chr15:50252348 | C | T | 7 | a0001c0004t0001g0046 a0001c0004t0001g0178 a0001c0005t0002g0177 others(4): Show |
11 | HG00099.hp1 HG00733.hp1 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.1041+82G>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 9/11 | chr15 | 50252348 | |||||||
| chr15:50252833 | G | A | 2 | a0001c0001t0001g0206 a0001c0001t0001g0208 |
2 | HG01255.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.788-59C>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 7/11 | chr15 | 50252833 | |||||||
| chr15:50252838 | T | C | 2 | a0001c0001t0001g0025 a0001c0001t0001g0080 |
4 | HG01884.hp1 HG02630.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.788-64A>G | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 7/11 | chr15 | 50252838 | |||||||
| chr15:50252893 | G | A | 2 | a0001c0001t0001g0073 a0001c0001t0001g0074 |
2 | NA18747.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.788-119C>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 7/11 | chr15 | 50252893 | |||||||
| chr15:50252895 | A | AG | 9 | a0001c0001t0001g0157 a0002c0002t0002g0028 a0002c0002t0002g0030 others(6): Show |
13 | HG00408.hp2 HG00423.hp2 HG00597.hp1 others(10): Show |
intron_variant | MODIFIER | c.788-122dupC | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 7/11 | chr15 | 50252895 | |||||||
| chr15:50252962 | T | A | 38 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0012 others(35): Show |
68 | HG00280.hp2 HG00423.hp1 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.788-188A>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 7/11 | chr15 | 50252962 | |||||||
| chr15:50252965 | G | T | 80 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(77): Show |
131 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(128): Show |
intron_variant | MODIFIER | c.788-191C>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 7/11 | chr15 | 50252965 | |||||||
| chr15:50252973 | A | G | 1 | a0001c0001t0001g0198 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.788-199T>C | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 7/11 | chr15 | 50252973 | |||||||
| chr15:50253049 | C | T | 8 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0025 others(5): Show |
15 | HG01243.hp1 HG01256.hp1 HG01258.hp1 others(12): Show |
intron_variant | MODIFIER | c.788-275G>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 7/11 | chr15 | 50253049 | |||||||
| chr15:50253118 | G | C | 1 | a0002c0008t0002g0130 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.788-344C>G | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 7/11 | chr15 | 50253118 | |||||||
| chr15:50253309 | T | G | 2 | a0001c0005t0001g0011 a0001c0005t0001g0050 |
5 | HG02258.hp1 HG02572.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.787+291A>C | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 7/11 | chr15 | 50253309 | |||||||
| chr15:50253358 | C | T | 1 | a0001c0001t0001g0173 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.787+242G>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 7/11 | chr15 | 50253358 | |||||||
| chr15:50253569 | G | A | 1 | a0001c0001t0001g0107 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.787+31C>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 7/11 | chr15 | 50253569 | |||||||
| chr15:50253773 | A | G | 12 | a0001c0001t0001g0157 a0001c0001t0001g0161 a0002c0002t0002g0028 others(9): Show |
18 | HG00408.hp2 HG00423.hp2 HG00597.hp1 others(15): Show |
intron_variant | MODIFIER | c.721-107T>C | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 6/11 | chr15 | 50253773 | |||||||
| chr15:50254329 | C | A | 2 | a0001c0001t0001g0153 a0001c0001t0001g0154 |
2 | HG01069.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.577-56G>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 5/11 | chr15 | 50254329 | |||||||
| chr15:50254353 | C | T | 3 | a0001c0004t0001g0046 a0001c0004t0001g0178 a0001c0005t0002g0177 |
4 | HG02615.hp2 HG02970.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.577-80G>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 5/11 | chr15 | 50254353 | |||||||
| chr15:50254733 | GTT | G | 28 | a0001c0001t0001g0009 a0001c0001t0001g0048 a0001c0001t0001g0049 others(25): Show |
41 | HG00423.hp2 HG01891.hp2 HG02027.hp1 others(38): Show |
intron_variant | MODIFIER | c.442-71_442-70delAA | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 4/11 | chr15 | 50254733 | |||||||
| chr15:50254736 | T | TCTCTCTC others(4): Show |
1 | a0001c0004t0001g0127 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.442-73_442-72insGA others(9): Show |
HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 4/11 | chr15 | 50254736 | |||||||
| chr15:50254736 | T | TTCTCTCT others(3): Show |
1 | a0001c0005t0001g0050 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.442-73_442-72insGA others(8): Show |
HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 4/11 | chr15 | 50254736 | |||||||
| chr15:50254736 | TTTTC | T | 37 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0018 others(34): Show |
82 | HG00438.hp1 HG00544.hp2 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.442-76_442-73delGA others(2): Show |
HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 4/11 | chr15 | 50254736 | |||||||
| chr15:50254736 | TTTTCTC | T | 4 | a0001c0001t0001g0098 a0001c0001t0001g0132 a0001c0001t0001g0144 others(1): Show |
4 | HG01256.hp2 HG02165.hp2 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.442-78_442-73delGA others(4): Show |
HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 4/11 | chr15 | 50254736 | |||||||
| chr15:50254738 | T | C | 19 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0037 others(16): Show |
28 | HG00140.hp2 HG00280.hp1 HG00597.hp1 others(25): Show |
intron_variant | MODIFIER | c.442-74A>G | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 4/11 | chr15 | 50254738 | |||||||
| chr15:50254738 | T | TTC | 8 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(5): Show |
27 | HG00323.hp2 HG00597.hp2 HG02129.hp1 others(24): Show |
intron_variant | MODIFIER | c.442-76_442-75dupGA | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 4/11 | chr15 | 50254738 | |||||||
| chr15:50254738 | T | TTCTC | 4 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0063 others(1): Show |
14 | HG00099.hp2 HG00140.hp1 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.442-78_442-75dupGA others(2): Show |
HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 4/11 | chr15 | 50254738 | |||||||
| chr15:50254738 | T | TTCTCTC | 4 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0054 others(1): Show |
4 | HG01168.hp2 HG01169.hp1 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.442-80_442-75dupGA others(4): Show |
HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 4/11 | chr15 | 50254738 | |||||||
| chr15:50254738 | T | TTCTCTCT others(1): Show |
4 | a0001c0004t0001g0046 a0002c0007t0001g0013 a0002c0007t0001g0053 others(1): Show |
5 | HG00099.hp1 HG01074.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.442-82_442-75dupGA others(6): Show |
HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 4/11 | chr15 | 50254738 | |||||||
| chr15:50254738 | T | TTCTCTCT others(3): Show |
3 | a0001c0004t0001g0178 a0001c0005t0002g0177 a0002c0007t0001g0013 |
4 | HG01099.hp2 HG02615.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.442-84_442-75dupGA others(8): Show |
HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 4/11 | chr15 | 50254738 | |||||||
| chr15:50254738 | T | TTCTCTCT others(5): Show |
1 | a0002c0007t0001g0013 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.442-86_442-75dupGA others(10): Show |
HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 4/11 | chr15 | 50254738 | |||||||
| chr15:50254738 | TTC | T | 14 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(11): Show |
19 | HG00408.hp1 HG00609.hp1 HG00621.hp1 others(16): Show |
intron_variant | MODIFIER | c.442-76_442-75delGA | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 4/11 | chr15 | 50254738 | |||||||
| chr15:50254738 | TTCTC | T | 13 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0064 others(10): Show |
20 | HG00738.hp1 HG00741.hp1 HG01069.hp2 others(17): Show |
intron_variant | MODIFIER | c.442-78_442-75delGA others(2): Show |
HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 4/11 | chr15 | 50254738 | |||||||
| chr15:50254738 | TTCTCTC | T | 35 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0012 others(32): Show |
63 | HG00280.hp2 HG00423.hp1 HG00642.hp1 others(60): Show |
intron_variant | MODIFIER | c.442-80_442-75delGA others(4): Show |
HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 4/11 | chr15 | 50254738 | |||||||
| chr15:50254738 | TTCTCTCT others(1): Show |
T | 12 | a0001c0001t0001g0008 a0001c0001t0001g0025 a0001c0001t0001g0080 others(9): Show |
19 | HG00323.hp1 HG00639.hp2 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.442-82_442-75delGA others(6): Show |
HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 4/11 | chr15 | 50254738 | |||||||
| chr15:50254738 | TTCTCTCT others(11): Show |
T | 3 | a0004c0006t0002g0021 a0004c0006t0002g0131 a0004c0006t0002g0213 |
6 | HG02145.hp1 HG02257.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.442-92_442-75delGA others(16): Show |
HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 4/11 | chr15 | 50254738 | |||||||
| chr15:50254740 | C | T | 1 | a0001c0001t0001g0001 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.442-76G>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 4/11 | chr15 | 50254740 | |||||||
| chr15:50254744 | C | T | 1 | a0001c0001t0001g0064 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.442-80G>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 4/11 | chr15 | 50254744 | |||||||
| chr15:50254772 | C | G | 6 | a0001c0001t0001g0143 a0001c0001t0001g0157 a0001c0001t0001g0174 others(3): Show |
6 | HG03041.hp1 HG03471.hp2 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.442-108G>C | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 4/11 | chr15 | 50254772 | |||||||
| chr15:50254774 | C | G | 56 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0012 others(53): Show |
95 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.442-110G>C | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 4/11 | chr15 | 50254774 | |||||||
| chr15:50254776 | C | CTCTCTCT others(1): Show |
3 | a0001c0004t0001g0128 a0001c0004t0001g0129 a0002c0007t0001g0052 |
3 | HG00733.hp1 HG02818.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.442-113_442-112ins others(8): Show |
HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 4/11 | chr15 | 50254776 | |||||||
| chr15:50254776 | C | CTG | 3 | a0001c0001t0001g0022 a0001c0001t0001g0033 a0001c0001t0001g0058 |
6 | HG01243.hp1 HG01884.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.442-114_442-113dup others(2): Show |
HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 4/11 | chr15 | 50254776 | |||||||
| chr15:50254776 | C | G | 60 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0012 others(57): Show |
99 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.442-112G>C | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 4/11 | chr15 | 50254776 | |||||||
| chr15:50254778 | G | C | 1 | a0001c0001t0001g0044 | 2 | NA18966.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.442-114C>G | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 4/11 | chr15 | 50254778 | |||||||
| chr15:50254987 | C | T | 1 | a0003c0003t0001g0186 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.442-323G>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 4/11 | chr15 | 50254987 | |||||||
| chr15:50255209 | G | A | 1 | a0001c0001t0001g0110 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.442-545C>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 4/11 | chr15 | 50255209 | |||||||
| chr15:50255673 | A | G | 1 | a0003c0003t0001g0167 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.442-1009T>C | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 4/11 | chr15 | 50255673 | |||||||
| chr15:50255690 | C | T | 1 | a0001c0004t0001g0127 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.442-1026G>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 4/11 | chr15 | 50255690 | |||||||
| chr15:50255691 | G | A | 4 | a0001c0001t0001g0017 a0001c0001t0001g0077 a0001c0001t0001g0078 others(1): Show |
7 | HG01123.hp1 HG01257.hp1 HG01346.hp1 others(4): Show |
intron_variant | MODIFIER | c.442-1027C>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 4/11 | chr15 | 50255691 | |||||||
| chr15:50255787 | C | T | 1 | a0001c0001t0001g0084 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.442-1123G>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 4/11 | chr15 | 50255787 | |||||||
| chr15:50255857 | A | G | 7 | a0001c0004t0001g0046 a0001c0004t0001g0178 a0001c0005t0002g0177 others(4): Show |
11 | HG00099.hp1 HG00733.hp1 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.442-1193T>C | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 4/11 | chr15 | 50255857 | |||||||
| chr15:50255971 | A | G | 8 | a0001c0001t0001g0163 a0001c0001t0001g0188 a0001c0004t0001g0125 others(5): Show |
11 | HG01109.hp2 HG02258.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.442-1307T>C | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 4/11 | chr15 | 50255971 | |||||||
| chr15:50256046 | C | T | 43 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0018 others(40): Show |
91 | HG00438.hp1 HG00544.hp2 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.441+1379G>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 4/11 | chr15 | 50256046 | |||||||
| chr15:50256058 | G | A | 1 | a0001c0001t0001g0079 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.441+1367C>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 4/11 | chr15 | 50256058 | |||||||
| chr15:50256058 | G | C | 2 | a0001c0001t0001g0025 a0001c0001t0001g0080 |
4 | HG01884.hp1 HG02630.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.441+1367C>G | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 4/11 | chr15 | 50256058 | |||||||
| chr15:50256121 | G | C | 3 | a0001c0004t0001g0046 a0001c0004t0001g0178 a0001c0005t0002g0177 |
4 | HG02615.hp2 HG02970.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.441+1304C>G | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 4/11 | chr15 | 50256121 | |||||||
| chr15:50256230 | C | T | 1 | a0001c0001t0001g0032 | 2 | NA18948.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.441+1195G>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 4/11 | chr15 | 50256230 | |||||||
| chr15:50256366 | G | A | 9 | a0001c0001t0001g0008 a0001c0001t0001g0096 a0001c0001t0001g0171 others(6): Show |
15 | HG00323.hp1 HG00639.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.441+1059C>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 4/11 | chr15 | 50256366 | |||||||
| chr15:50256470 | C | T | 1 | a0001c0004t0001g0125 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.441+955G>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 4/11 | chr15 | 50256470 | |||||||
| chr15:50256630 | T | C | 1 | a0001c0001t0001g0119 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.441+795A>G | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 4/11 | chr15 | 50256630 | |||||||
| chr15:50256688 | G | A | 1 | a0001c0001t0001g0202 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.441+737C>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 4/11 | chr15 | 50256688 | |||||||
| chr15:50256759 | T | C | 1 | a0001c0001t0001g0080 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.441+666A>G | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 4/11 | chr15 | 50256759 | |||||||
| chr15:50256865 | T | C | 3 | a0004c0006t0002g0021 a0004c0006t0002g0131 a0004c0006t0002g0213 |
6 | HG02145.hp1 HG02257.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.441+560A>G | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 4/11 | chr15 | 50256865 | |||||||
| chr15:50256899 | A | C | 2 | a0001c0001t0001g0192 a0001c0001t0001g0193 |
2 | HG01109.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.441+526T>G | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 4/11 | chr15 | 50256899 | |||||||
| chr15:50257007 | G | A | 2 | a0001c0001t0001g0081 a0001c0001t0001g0082 |
2 | HG02965.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.441+418C>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 4/11 | chr15 | 50257007 | |||||||
| chr15:50257380 | G | A | 1 | a0002c0008t0002g0210 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.441+45C>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 4/11 | chr15 | 50257380 | |||||||
| chr15:50257391 | C | G | 4 | a0002c0008t0002g0210 a0004c0006t0002g0021 a0004c0006t0002g0131 others(1): Show |
7 | HG02145.hp1 HG02257.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.441+34G>C | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 4/11 | chr15 | 50257391 | |||||||
| chr15:50257395 | A | T | 4 | a0002c0008t0002g0210 a0004c0006t0002g0021 a0004c0006t0002g0131 others(1): Show |
7 | HG02145.hp1 HG02257.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.441+30T>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 4/11 | chr15 | 50257395 | |||||||
| chr15:50257827 | C | T | 1 | a0002c0008t0002g0210 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.319-280G>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 3/11 | chr15 | 50257827 | |||||||
| chr15:50257870 | T | A | 1 | a0002c0008t0002g0210 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.319-323A>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 3/11 | chr15 | 50257870 | |||||||
| chr15:50258041 | C | T | 1 | a0001c0001t0001g0063 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.318+363G>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 3/11 | chr15 | 50258041 | |||||||
| chr15:50258200 | A | G | 1 | a0001c0001t0001g0062 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.318+204T>C | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 3/11 | chr15 | 50258200 | |||||||
| chr15:50258364 | A | G | 1 | a0001c0001t0001g0097 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.318+40T>C | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 3/11 | chr15 | 50258364 | |||||||
| chr15:50258378 | G | A | 3 | a0001c0001t0001g0056 a0001c0001t0001g0111 a0001c0001t0001g0112 |
3 | HG02074.hp2 NA18977.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.318+26C>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 3/11 | chr15 | 50258378 | |||||||
| chr15:50258544 | G | T | 5 | a0001c0004t0001g0125 a0001c0004t0001g0127 a0001c0004t0001g0128 others(2): Show |
5 | HG02818.hp2 HG02896.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.205-27C>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50258544 | |||||||
| chr15:50258703 | C | T | 38 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0012 others(35): Show |
68 | HG00280.hp2 HG00423.hp1 HG00642.hp1 others(65): Show |
intron_variant | MODIFIER | c.205-186G>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50258703 | |||||||
| chr15:50258785 | C | T | 1 | a0001c0001t0001g0061 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.205-268G>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50258785 | |||||||
| chr15:50258813 | G | A | 1 | a0001c0001t0001g0058 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.205-296C>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50258813 | |||||||
| chr15:50258886 | T | C | 142 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(139): Show |
251 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(248): Show |
intron_variant | MODIFIER | c.205-369A>G | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50258886 | |||||||
| chr15:50258906 | A | T | 82 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(79): Show |
151 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(148): Show |
intron_variant | MODIFIER | c.205-389T>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50258906 | |||||||
| chr15:50258988 | A | G | 104 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(101): Show |
183 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.205-471T>C | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50258988 | |||||||
| chr15:50259005 | C | CA | 102 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(99): Show |
178 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(175): Show |
intron_variant | MODIFIER | c.205-489dupT | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50259005 | |||||||
| chr15:50259005 | C | CAA | 2 | a0004c0006t0002g0021 a0004c0006t0002g0213 |
5 | HG02145.hp1 HG02257.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.205-490_205-489dup others(2): Show |
HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50259005 | |||||||
| chr15:50259140 | C | T | 1 | a0001c0012t0001g0126 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.205-623G>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50259140 | |||||||
| chr15:50259163 | A | G | 33 | a0001c0001t0001g0173 a0001c0001t0001g0174 a0001c0001t0001g0175 others(30): Show |
50 | HG00099.hp1 HG00558.hp2 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.205-646T>C | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50259163 | |||||||
| chr15:50259389 | T | C | 1 | a0001c0001t0001g0155 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.205-872A>G | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50259389 | |||||||
| chr15:50259398 | G | A | 11 | a0001c0001t0001g0188 a0003c0003t0001g0010 a0003c0003t0001g0167 others(8): Show |
15 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(12): Show |
intron_variant | MODIFIER | c.205-881C>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50259398 | |||||||
| chr15:50259435 | G | T | 70 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(67): Show |
132 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.205-918C>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50259435 | |||||||
| chr15:50259444 | G | T | 1 | a0001c0001t0001g0191 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.205-927C>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50259444 | |||||||
| chr15:50259507 | G | A | 11 | a0003c0003t0001g0010 a0003c0003t0001g0020 a0003c0003t0001g0167 others(8): Show |
18 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(15): Show |
intron_variant | MODIFIER | c.205-990C>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50259507 | |||||||
| chr15:50259577 | A | G | 1 | a0001c0001t0001g0188 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.205-1060T>C | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50259577 | |||||||
| chr15:50259658 | G | T | 11 | a0003c0003t0001g0010 a0003c0003t0001g0020 a0003c0003t0001g0167 others(8): Show |
18 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(15): Show |
intron_variant | MODIFIER | c.205-1141C>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50259658 | |||||||
| chr15:50259722 | C | T | 2 | a0004c0006t0002g0021 a0004c0006t0002g0213 |
5 | HG02145.hp1 HG02257.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.205-1205G>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50259722 | |||||||
| chr15:50259733 | C | T | 38 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0012 others(35): Show |
68 | HG00280.hp2 HG00423.hp1 HG00642.hp1 others(65): Show |
intron_variant | MODIFIER | c.205-1216G>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50259733 | |||||||
| chr15:50260023 | CT | C | 9 | a0001c0001t0001g0008 a0001c0001t0001g0096 a0001c0001t0001g0171 others(6): Show |
15 | HG00323.hp1 HG00639.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.205-1507delA | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50260023 | |||||||
| chr15:50260023 | CTT | C | 98 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(95): Show |
187 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(184): Show |
intron_variant | MODIFIER | c.205-1508_205-1507d others(4): Show |
HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50260023 | |||||||
| chr15:50260105 | C | T | 1 | a0001c0001t0001g0187 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.205-1588G>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50260105 | |||||||
| chr15:50260153 | C | T | 1 | a0001c0004t0001g0142 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.205-1636G>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50260153 | |||||||
| chr15:50260172 | C | G | 1 | a0001c0004t0001g0125 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.205-1655G>C | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50260172 | |||||||
| chr15:50260175 | C | T | 1 | a0002c0008t0002g0130 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.205-1658G>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50260175 | |||||||
| chr15:50260256 | C | A | 2 | a0001c0001t0001g0188 a0002c0008t0002g0210 |
2 | HG02976.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.205-1739G>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50260256 | |||||||
| chr15:50260301 | A | G | 202 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(199): Show |
401 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(398): Show |
intron_variant | MODIFIER | c.205-1784T>C | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50260301 | |||||||
| chr15:50260388 | G | A | 38 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0012 others(35): Show |
68 | HG00280.hp2 HG00423.hp1 HG00642.hp1 others(65): Show |
intron_variant | MODIFIER | c.205-1871C>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50260388 | |||||||
| chr15:50260554 | A | T | 1 | a0001c0004t0001g0178 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.205-2037T>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50260554 | |||||||
| chr15:50260658 | C | T | 79 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(76): Show |
138 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(135): Show |
intron_variant | MODIFIER | c.205-2141G>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50260658 | |||||||
| chr15:50260803 | G | A | 48 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0012 others(45): Show |
85 | HG00280.hp2 HG00423.hp1 HG00609.hp1 others(82): Show |
intron_variant | MODIFIER | c.205-2286C>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50260803 | |||||||
| chr15:50260830 | G | T | 1 | a0001c0001t0001g0032 | 2 | NA18948.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.205-2313C>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50260830 | |||||||
| chr15:50260880 | A | G | 49 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0031 others(46): Show |
81 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(78): Show |
intron_variant | MODIFIER | c.204+2355T>C | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50260880 | |||||||
| chr15:50261176 | T | G | 1 | a0002c0002t0002g0030 | 3 | NA18980.hp2 NA18981.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.204+2059A>C | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50261176 | |||||||
| chr15:50261226 | G | A | 1 | a0002c0002t0002g0030 | 3 | NA18980.hp2 NA18981.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.204+2009C>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50261226 | |||||||
| chr15:50261227 | C | A | 1 | a0001c0001t0001g0095 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.204+2008G>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50261227 | |||||||
| chr15:50261307 | T | G | 1 | a0001c0001t0001g0163 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.204+1928A>C | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50261307 | |||||||
| chr15:50261574 | A | C | 1 | a0001c0001t0001g0059 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.204+1661T>G | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50261574 | |||||||
| chr15:50261623 | C | CA | 79 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(76): Show |
138 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.204+1611dupT | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50261623 | |||||||
| chr15:50261623 | C | CAA | 16 | a0001c0001t0001g0037 a0001c0001t0001g0049 a0001c0001t0001g0114 others(13): Show |
19 | HG00280.hp1 HG00597.hp1 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.204+1610_204+1611d others(4): Show |
HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50261623 | |||||||
| chr15:50261623 | CAAAAAAA others(3): Show |
C | 2 | a0001c0001t0001g0022 a0001c0001t0001g0058 |
4 | HG01243.hp1 HG02886.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.204+1602_204+1611d others(12): Show |
HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50261623 | |||||||
| chr15:50261675 | T | A | 1 | a0001c0001t0001g0057 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.204+1560A>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50261675 | |||||||
| chr15:50261678 | T | A | 1 | a0001c0001t0001g0057 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.204+1557A>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50261678 | |||||||
| chr15:50261682 | C | A | 1 | a0001c0001t0001g0057 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.204+1553G>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50261682 | |||||||
| chr15:50261683 | C | A | 1 | a0001c0001t0001g0057 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.204+1552G>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50261683 | |||||||
| chr15:50261686 | C | T | 1 | a0001c0001t0001g0057 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.204+1549G>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50261686 | |||||||
| chr15:50261688 | C | G | 1 | a0001c0001t0001g0057 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.204+1547G>C | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50261688 | |||||||
| chr15:50261691 | C | A | 1 | a0001c0001t0001g0057 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.204+1544G>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50261691 | |||||||
| chr15:50261703 | T | A | 1 | a0001c0001t0001g0057 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.204+1532A>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50261703 | |||||||
| chr15:50261709 | T | A | 1 | a0001c0001t0001g0057 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.204+1526A>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50261709 | |||||||
| chr15:50261711 | A | T | 1 | a0001c0001t0001g0057 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.204+1524T>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50261711 | |||||||
| chr15:50261712 | C | CTT | 6 | a0001c0004t0001g0046 a0001c0004t0001g0178 a0001c0005t0002g0177 others(3): Show |
10 | HG00099.hp1 HG00733.hp1 HG01074.hp2 others(7): Show |
intron_variant | MODIFIER | c.204+1521_204+1522d others(4): Show |
HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50261712 | |||||||
| chr15:50261712 | CT | C | 49 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0012 others(46): Show |
86 | HG00280.hp2 HG00423.hp1 HG00609.hp1 others(83): Show |
intron_variant | MODIFIER | c.204+1522delA | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50261712 | |||||||
| chr15:50261721 | T | C | 1 | a0001c0001t0001g0057 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.204+1514A>G | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50261721 | |||||||
| chr15:50261740 | G | A | 1 | a0002c0008t0002g0210 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.204+1495C>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50261740 | |||||||
| chr15:50261743 | C | T | 1 | a0001c0001t0001g0057 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.204+1492G>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50261743 | |||||||
| chr15:50261747 | T | A | 1 | a0001c0001t0001g0057 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.204+1488A>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50261747 | |||||||
| chr15:50261748 | T | A | 1 | a0001c0001t0001g0057 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.204+1487A>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50261748 | |||||||
| chr15:50261754 | G | A | 1 | a0001c0001t0001g0057 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.204+1481C>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50261754 | |||||||
| chr15:50261755 | G | A | 1 | a0001c0001t0001g0057 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.204+1480C>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50261755 | |||||||
| chr15:50261756 | C | T | 1 | a0001c0001t0001g0057 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.204+1479G>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50261756 | |||||||
| chr15:50261757 | T | A | 1 | a0001c0001t0001g0057 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.204+1478A>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50261757 | |||||||
| chr15:50261760 | A | G | 1 | a0001c0001t0001g0190 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.204+1475T>C | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50261760 | |||||||
| chr15:50261763 | G | T | 1 | a0001c0001t0001g0057 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.204+1472C>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50261763 | |||||||
| chr15:50261769 | G | T | 1 | a0001c0001t0001g0057 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.204+1466C>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50261769 | |||||||
| chr15:50261776 | C | G | 1 | a0001c0001t0001g0057 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.204+1459G>C | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50261776 | |||||||
| chr15:50261779 | A | T | 1 | a0001c0001t0001g0057 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.204+1456T>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50261779 | |||||||
| chr15:50261790 | A | T | 1 | a0001c0001t0001g0057 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.204+1445T>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50261790 | |||||||
| chr15:50261796 | G | A | 1 | a0001c0001t0001g0057 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.204+1439C>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50261796 | |||||||
| chr15:50261803 | G | A | 40 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0012 others(37): Show |
73 | HG00280.hp2 HG00423.hp1 HG00642.hp1 others(70): Show |
intron_variant | MODIFIER | c.204+1432C>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50261803 | |||||||
| chr15:50261805 | G | A | 1 | a0001c0001t0001g0120 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.204+1430C>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50261805 | |||||||
| chr15:50261806 | T | C | 1 | a0001c0001t0001g0057 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.204+1429A>G | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50261806 | |||||||
| chr15:50261829 | C | G | 1 | a0001c0001t0001g0057 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.204+1406G>C | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50261829 | |||||||
| chr15:50261831 | T | C | 1 | a0001c0001t0001g0057 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.204+1404A>G | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50261831 | |||||||
| chr15:50261832 | C | T | 1 | a0001c0001t0001g0057 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.204+1403G>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50261832 | |||||||
| chr15:50261833 | C | T | 1 | a0001c0001t0001g0057 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.204+1402G>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50261833 | |||||||
| chr15:50261835 | A | G | 5 | a0001c0004t0001g0125 a0001c0004t0001g0127 a0001c0004t0001g0128 others(2): Show |
5 | HG02818.hp2 HG02896.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.204+1400T>C | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50261835 | |||||||
| chr15:50261898 | G | A | 1 | a0001c0001t0001g0121 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.204+1337C>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50261898 | |||||||
| chr15:50262075 | A | C | 2 | a0004c0006t0002g0021 a0004c0006t0002g0213 |
5 | HG02145.hp1 HG02257.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.204+1160T>G | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50262075 | |||||||
| chr15:50262113 | C | T | 1 | a0002c0008t0002g0189 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.204+1122G>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50262113 | |||||||
| chr15:50262198 | A | T | 1 | a0001c0004t0001g0125 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.204+1037T>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50262198 | |||||||
| chr15:50262301 | T | C | 2 | a0001c0001t0001g0188 a0004c0006t0002g0172 |
2 | HG01109.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.204+934A>G | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50262301 | |||||||
| chr15:50262332 | C | G | 1 | a0003c0003t0001g0181 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.204+903G>C | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50262332 | |||||||
| chr15:50262336 | G | A | 1 | a0001c0001t0001g0122 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.204+899C>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50262336 | |||||||
| chr15:50262426 | G | A | 2 | a0001c0001t0001g0041 a0001c0001t0001g0141 |
3 | HG01081.hp1 HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.204+809C>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50262426 | |||||||
| chr15:50262496 | G | A | 19 | a0001c0001t0001g0005 a0001c0001t0001g0019 a0001c0001t0001g0042 others(16): Show |
36 | HG00280.hp2 HG00423.hp1 HG00673.hp2 others(33): Show |
intron_variant | MODIFIER | c.204+739C>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50262496 | |||||||
| chr15:50262814 | C | T | 87 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(84): Show |
151 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(148): Show |
intron_variant | MODIFIER | c.204+421G>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50262814 | |||||||
| chr15:50262904 | A | G | 1 | a0001c0010t0001g0124 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.204+331T>C | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50262904 | |||||||
| chr15:50262930 | TC | T | 7 | a0001c0001t0001g0056 a0003c0003t0001g0010 a0003c0003t0001g0181 others(4): Show |
11 | HG00609.hp1 HG00738.hp1 HG00741.hp1 others(8): Show |
intron_variant | MODIFIER | c.204+304delG | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50262930 | |||||||
| chr15:50262964 | C | A | 1 | a0001c0001t0001g0209 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.204+271G>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50262964 | |||||||
| chr15:50263039 | A | G | 33 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0031 others(30): Show |
58 | HG00323.hp1 HG00544.hp2 HG00639.hp2 others(55): Show |
intron_variant | MODIFIER | c.204+196T>C | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 2/11 | chr15 | 50263039 | |||||||
| chr15:50263484 | C | T | 1 | a0002c0007t0001g0052 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.32-77G>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 1/11 | chr15 | 50263484 | |||||||
| chr15:50263513 | T | C | 120 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(117): Show |
205 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(202): Show |
intron_variant | MODIFIER | c.32-106A>G | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 1/11 | chr15 | 50263513 | |||||||
| chr15:50263583 | C | T | 1 | a0001c0001t0001g0055 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.32-176G>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 1/11 | chr15 | 50263583 | |||||||
| chr15:50263661 | G | T | 3 | a0002c0007t0001g0013 a0002c0007t0001g0052 a0002c0007t0001g0053 |
6 | HG00099.hp1 HG00733.hp1 HG01074.hp2 others(3): Show |
intron_variant | MODIFIER | c.32-254C>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 1/11 | chr15 | 50263661 | |||||||
| chr15:50263667 | G | A | 36 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0031 others(33): Show |
64 | HG00323.hp1 HG00544.hp2 HG00639.hp2 others(61): Show |
intron_variant | MODIFIER | c.32-260C>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 1/11 | chr15 | 50263667 | |||||||
| chr15:50263758 | C | A | 4 | a0001c0001t0001g0173 a0001c0001t0001g0174 a0001c0001t0001g0175 others(1): Show |
4 | HG01891.hp2 HG03041.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.32-351G>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 1/11 | chr15 | 50263758 | |||||||
| chr15:50263776 | G | C | 3 | a0001c0004t0001g0046 a0001c0004t0001g0178 a0001c0005t0002g0177 |
4 | HG02615.hp2 HG02970.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.32-369C>G | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 1/11 | chr15 | 50263776 | |||||||
| chr15:50263776 | G | T | 1 | a0001c0001t0001g0054 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.32-369C>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 1/11 | chr15 | 50263776 | |||||||
| chr15:50263948 | G | A | 1 | a0002c0008t0002g0210 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.32-541C>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 1/11 | chr15 | 50263948 | |||||||
| chr15:50264229 | G | A | 2 | a0004c0006t0002g0021 a0004c0006t0002g0213 |
5 | HG02145.hp1 HG02257.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.32-822C>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 1/11 | chr15 | 50264229 | |||||||
| chr15:50264395 | G | A | 1 | a0002c0002t0002g0179 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.32-988C>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 1/11 | chr15 | 50264395 | |||||||
| chr15:50264424 | A | G | 3 | a0001c0001t0001g0031 a0001c0001t0001g0187 a0001c0001t0001g0211 |
5 | HG00544.hp2 NA18942.hp2 NA18967.hp2 others(2): Show |
intron_variant | MODIFIER | c.32-1017T>C | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 1/11 | chr15 | 50264424 | |||||||
| chr15:50264769 | C | A | 1 | a0001c0001t0001g0211 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.31+824G>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 1/11 | chr15 | 50264769 | |||||||
| chr15:50264800 | C | G | 10 | a0002c0007t0001g0013 a0002c0007t0001g0052 a0002c0007t0001g0053 others(7): Show |
17 | HG00099.hp1 HG00609.hp1 HG00733.hp1 others(14): Show |
intron_variant | MODIFIER | c.31+793G>C | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 1/11 | chr15 | 50264800 | |||||||
| chr15:50264879 | G | C | 1 | a0001c0004t0001g0180 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.31+714C>G | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 1/11 | chr15 | 50264879 | |||||||
| chr15:50264915 | A | G | 1 | a0001c0001t0001g0051 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.31+678T>C | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 1/11 | chr15 | 50264915 | |||||||
| chr15:50264962 | G | A | 7 | a0003c0003t0001g0010 a0003c0003t0001g0181 a0003c0003t0001g0182 others(4): Show |
11 | HG00609.hp1 HG00738.hp1 HG00741.hp1 others(8): Show |
intron_variant | MODIFIER | c.31+631C>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 1/11 | chr15 | 50264962 | |||||||
| chr15:50265134 | T | G | 1 | a0002c0007t0001g0212 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.31+459A>C | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 1/11 | chr15 | 50265134 | |||||||
| chr15:50265185 | A | T | 2 | a0004c0006t0002g0021 a0004c0006t0002g0213 |
5 | HG02145.hp1 HG02257.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.31+408T>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 1/11 | chr15 | 50265185 | |||||||
| chr15:50265255 | C | A | 1 | a0004c0006t0002g0213 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.31+338G>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 1/11 | chr15 | 50265255 | |||||||
| chr15:50265403 | G | T | 1 | a0001c0001t0001g0012 | 4 | HG01496.hp2 HG02717.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.31+190C>A | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 1/11 | chr15 | 50265403 | |||||||
| chr15:50265532 | C | G | 2 | a0001c0005t0001g0011 a0001c0005t0001g0050 |
5 | HG02258.hp1 HG02572.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.31+61G>C | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 1/11 | chr15 | 50265532 | |||||||
| chr15:50265541 | G | A | 34 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0031 others(31): Show |
61 | HG00323.hp1 HG00544.hp2 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.31+52C>T | HDC | ENSG00000140287.11 | transcript | ENST00000267845.8 | protein_coding | 1/11 | chr15 | 50265541 |