Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 732 |
| ensemblid | ENSG00000021852.14 |
| hgncid | 1353 |
| symbol | C8B |
| name | complement C8 beta chain |
| refseq_nuc | NM_000066.4 |
| refseq_prot | NP_000057.3 |
| ensembl_nuc | ENST00000371237.9 |
| ensembl_prot | ENSP00000360281.4 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 56929207 |
| end | 56966015 |
| strand | - |
| ver | v1.2 |
| region | chr1:56929207-56966015 |
| region5000 | chr1:56924207-56971015 |
| regionname0 | C8B_chr1_56929207_56966015 |
| regionname5000 | C8B_chr1_56924207_56971015 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 591 | 382 | 91 | 68 | 165 | 16 | 41 | 118 | C8B_chr1_56924207_56971015 | C8B | MKNSR others(586): Show |
chr1 | 56924207 | 56971015 |
| a0002 | 0/0 | 591 | 8 | 5 | 2 | 0 | 0 | 1 | 0 | C8B_chr1_56924207_56971015 | C8B | MKNSR others(586): Show |
chr1 | 56924207 | 56971015 |
| a0003 | 1/0 | 591 | 6 | 0 | 2 | 0 | 0 | 3 | 0 | C8B_chr1_56924207_56971015 | C8B | MKNSR others(586): Show |
chr1 | 56924207 | 56971015 |
| a0004 | 0/0 | 591 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | MKNSR others(586): Show |
chr1 | 56924207 | 56971015 |
| a0005 | 0/0 | 591 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | C8B_chr1_56924207_56971015 | C8B | MKNSR others(586): Show |
chr1 | 56924207 | 56971015 |
| a0006 | 0/0 | 591 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | MKNSR others(586): Show |
chr1 | 56924207 | 56971015 |
| a0007 | 0/0 | 591 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | MKNSR others(586): Show |
chr1 | 56924207 | 56971015 |
| a0008 | 0/0 | 591 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | MKNSR others(586): Show |
chr1 | 56924207 | 56971015 |
| a0009 | 0/0 | 591 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | MKNSR others(586): Show |
chr1 | 56924207 | 56971015 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1773 | 376 | 88 | 67 | 165 | 16 | 39 | C8B_chr1_56924207_56971015 | C8B | ATGAA others(1768): Show |
chr1 | 56924207 | 56971015 | ||
| a0001c0004 | 0/0 | 1773 | 4 | 3 | 1 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | ATGAA others(1768): Show |
chr1 | 56924207 | 56971015 | ||
| a0001c0005 | 0/0 | 1773 | 2 | 0 | 0 | 0 | 0 | 2 | C8B_chr1_56924207_56971015 | C8B | ATGAA others(1768): Show |
chr1 | 56924207 | 56971015 | ||
| a0002c0002 | 0/0 | 1773 | 8 | 5 | 2 | 0 | 0 | 1 | C8B_chr1_56924207_56971015 | C8B | ATGAA others(1768): Show |
chr1 | 56924207 | 56971015 | ||
| a0003c0003 | 1/0 | 1773 | 6 | 0 | 2 | 0 | 0 | 3 | C8B_chr1_56924207_56971015 | C8B | ATGAA others(1768): Show |
chr1 | 56924207 | 56971015 | ||
| a0004c0010 | 0/0 | 1773 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | ATGAA others(1768): Show |
chr1 | 56924207 | 56971015 | ||
| a0005c0008 | 0/0 | 1773 | 1 | 0 | 0 | 0 | 0 | 1 | C8B_chr1_56924207_56971015 | C8B | ATGAA others(1768): Show |
chr1 | 56924207 | 56971015 | ||
| a0006c0009 | 0/0 | 1773 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | ATGAA others(1768): Show |
chr1 | 56924207 | 56971015 | ||
| a0007c0011 | 0/0 | 1773 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | ATGAA others(1768): Show |
chr1 | 56924207 | 56971015 | ||
| a0008c0006 | 0/0 | 1773 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | ATGAA others(1768): Show |
chr1 | 56924207 | 56971015 | ||
| a0009c0007 | 0/0 | 1773 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | ATGAA others(1768): Show |
chr1 | 56924207 | 56971015 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2040 | 242 | 74 | 45 | 95 | 10 | 18 | C8B_chr1_56924207_56971015 | C8B | GGCAC others(2035): Show |
chr1 | 56924207 | 56971015 |
| a0001c0001t0002 | 0/1 | 2040 | 130 | 14 | 22 | 69 | 5 | 19 | C8B_chr1_56924207_56971015 | C8B | GGCAC others(2035): Show |
chr1 | 56924207 | 56971015 |
| a0001c0001t0003 | 0/0 | 2040 | 2 | 0 | 0 | 1 | 1 | 0 | C8B_chr1_56924207_56971015 | C8B | GGCAC others(2035): Show |
chr1 | 56924207 | 56971015 |
| a0001c0001t0004 | 0/0 | 2040 | 1 | 0 | 0 | 0 | 0 | 1 | C8B_chr1_56924207_56971015 | C8B | GGCAC others(2035): Show |
chr1 | 56924207 | 56971015 |
| a0001c0001t0005 | 0/0 | 2040 | 1 | 0 | 0 | 0 | 0 | 1 | C8B_chr1_56924207_56971015 | C8B | GGCAT others(2035): Show |
chr1 | 56924207 | 56971015 |
| a0001c0004t0001 | 0/0 | 2040 | 4 | 3 | 1 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | GGCAC others(2035): Show |
chr1 | 56924207 | 56971015 |
| a0001c0005t0001 | 0/0 | 2040 | 2 | 0 | 0 | 0 | 0 | 2 | C8B_chr1_56924207_56971015 | C8B | GGCAC others(2035): Show |
chr1 | 56924207 | 56971015 |
| a0002c0002t0001 | 0/0 | 2040 | 7 | 5 | 2 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | GGCAC others(2035): Show |
chr1 | 56924207 | 56971015 |
| a0002c0002t0002 | 0/0 | 2040 | 1 | 0 | 0 | 0 | 0 | 1 | C8B_chr1_56924207_56971015 | C8B | GGCAC others(2035): Show |
chr1 | 56924207 | 56971015 |
| a0003c0003t0001 | 1/0 | 2040 | 5 | 0 | 1 | 0 | 0 | 3 | C8B_chr1_56924207_56971015 | C8B | GGCAC others(2035): Show |
chr1 | 56924207 | 56971015 |
| a0003c0003t0002 | 0/0 | 2040 | 1 | 0 | 1 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | GGCAC others(2035): Show |
chr1 | 56924207 | 56971015 |
| a0004c0010t0001 | 0/0 | 2040 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | GGCAC others(2035): Show |
chr1 | 56924207 | 56971015 |
| a0005c0008t0001 | 0/0 | 2040 | 1 | 0 | 0 | 0 | 0 | 1 | C8B_chr1_56924207_56971015 | C8B | GGCAC others(2035): Show |
chr1 | 56924207 | 56971015 |
| a0006c0009t0001 | 0/0 | 2040 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | GGCAC others(2035): Show |
chr1 | 56924207 | 56971015 |
| a0007c0011t0001 | 0/0 | 2040 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | GGCAC others(2035): Show |
chr1 | 56924207 | 56971015 |
| a0008c0006t0001 | 0/0 | 2040 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | GGCAC others(2035): Show |
chr1 | 56924207 | 56971015 |
| a0009c0007t0002 | 0/0 | 2040 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | GGCAC others(2035): Show |
chr1 | 56924207 | 56971015 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 11 | 0 | 0 | 11 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0003 | 0/0 | 7 | 0 | 0 | 6 | 0 | 1 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0008 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0009 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0010 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0012 | 0/0 | 4 | 0 | 2 | 0 | 1 | 1 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0014 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0020 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0044 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0046 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0047 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0052 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0053 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0054 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0055 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0056 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0057 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0002g0002 | 0/0 | 7 | 0 | 0 | 6 | 0 | 1 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0002g0004 | 0/0 | 6 | 0 | 0 | 5 | 0 | 1 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0002g0005 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0002g0007 | 0/0 | 5 | 1 | 0 | 4 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0002g0011 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0002g0015 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0002g0017 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0002g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0002g0027 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0002g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0002g0033 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0002g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0002g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0002g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0002g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0002g0048 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0002g0049 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0002g0058 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0002g0059 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0002g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0002g0134 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0002g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0002g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0002g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0002g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0003g0051 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0004g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0001t0005g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0004t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0004t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0004t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0005t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0001c0005t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0002c0002t0001g0050 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0002c0002t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0002c0002t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0002c0002t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0002c0002t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0002c0002t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0002c0002t0002g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0003c0003t0001g0006 | 1/0 | 5 | 0 | 1 | 0 | 0 | 3 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0003c0003t0002g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0004c0010t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0005c0008t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0006c0009t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0007c0011t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0008c0006t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| a0009c0007t0002g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0108 | EUR | GBR | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0118 | EUR | GBR | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0135 | EUR | GBR | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0216 | EUR | GBR | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0208 | EUR | FIN | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0263 | EUR | FIN | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0031 | EUR | FIN | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0105 | EUR | FIN | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | CHS | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | CHS | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG00423 | hp2 | a0001 | c0001 | t0003 | g0051 | EAS | CHS | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0212 | EAS | CHS | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0255 | EAS | CHS | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0119 | EAS | CHS | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | CHS | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0080 | EAS | CHS | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0240 | EAS | CHS | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | CHS | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | CHS | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0266 | EAS | CHS | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG00621 | hp2 | a0004 | c0010 | t0001 | g0107 | EAS | CHS | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG00639 | hp1 | a0003 | c0003 | t0002 | g0235 | AMR | PUR | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0147 | AMR | PUR | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | CHS | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | PUR | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0190 | AMR | PUR | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0259 | AMR | PUR | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | PUR | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0201 | AMR | PUR | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG01070 | hp1 | a0002 | c0002 | t0001 | g0283 | AMR | PUR | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG01074 | hp1 | a0003 | c0003 | t0001 | g0006 | AMR | PUR | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0253 | AMR | PUR | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0239 | AMR | PUR | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | PUR | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | PUR | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0242 | AMR | PUR | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG01192 | hp1 | a0002 | c0002 | t0001 | g0223 | AMR | PUR | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0071 | AMR | PUR | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG01243 | hp1 | a0001 | c0004 | t0001 | g0229 | AMR | PUR | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0241 | AMR | CLM | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0015 | AMR | CLM | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0059 | AMR | CLM | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | CLM | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0218 | AMR | CLM | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0059 | AMR | CLM | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0238 | AMR | CLM | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0027 | AMR | CLM | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | CLM | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0046 | AMR | CLM | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0129 | AMR | CLM | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0217 | AMR | CLM | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | CLM | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0015 | AMR | CLM | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0209 | AMR | CLM | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0164 | EUR | IBS | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0195 | EUR | IBS | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG01517 | hp1 | a0001 | c0001 | t0003 | g0051 | EUR | IBS | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0194 | EUR | IBS | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0091 | AFR | ACB | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | ACB | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG01891 | hp1 | a0002 | c0002 | t0001 | g0050 | AFR | ACB | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | ACB | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0033 | AMR | PEL | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0165 | AMR | PEL | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0088 | AMR | PEL | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0037 | AMR | PEL | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | PEL | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0011 | AMR | PEL | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | PEL | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | PEL | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | PEL | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0011 | AMR | PEL | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0011 | AMR | PEL | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0188 | AMR | PEL | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0015 | AMR | PEL | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | PEL | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | KHV | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | KHV | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | KHV | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0075 | EAS | KHV | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0081 | EAS | KHV | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | ACB | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0186 | AFR | ACB | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | KHV | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0202 | EAS | KHV | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | KHV | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | KHV | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0060 | EAS | KHV | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | KHV | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | KHV | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | KHV | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0196 | EAS | KHV | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0076 | EAS | KHV | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | KHV | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | KHV | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | ACB | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | ACB | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | CDX | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0225 | EAS | CDX | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0159 | EAS | CDX | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0179 | AFR | ACB | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0276 | AFR | ACB | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0172 | AFR | ACB | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | ACB | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG02280 | hp1 | a0002 | c0002 | t0001 | g0176 | AFR | ACB | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | ACB | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0037 | AMR | PEL | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0015 | AMR | PEL | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0169 | AMR | PEL | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | PEL | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | ACB | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0185 | AFR | ACB | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0043 | EAS | KHV | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | KHV | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0213 | AFR | GWD | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0222 | AFR | GWD | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0125 | SAS | PJL | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | GWD | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0231 | AFR | GWD | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | GWD | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0146 | AFR | GWD | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | GWD | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | GWD | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG02683 | hp1 | a0003 | c0003 | t0001 | g0006 | SAS | PJL | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG02683 | hp2 | a0005 | c0008 | t0001 | g0268 | SAS | PJL | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0141 | SAS | PJL | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0247 | SAS | PJL | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | GWD | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | GWD | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG02723 | hp2 | a0002 | c0002 | t0001 | g0224 | AFR | GWD | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0054 | SAS | PJL | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG02735 | hp2 | a0001 | c0001 | t0004 | g0139 | SAS | PJL | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0048 | SAS | PJL | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0230 | SAS | PJL | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG02809 | hp1 | a0001 | c0004 | t0001 | g0153 | AFR | GWD | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | GWD | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | GWD | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | GWD | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | GWD | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0221 | AFR | GWD | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0211 | AFR | GWD | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | GWD | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | GWD | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | ESN | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | ESN | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | ESN | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | ESN | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | ESN | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | ESN | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | ESN | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG02976 | hp2 | a0006 | c0009 | t0001 | g0064 | AFR | ESN | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0233 | AFR | GWD | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | GWD | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | MSL | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | MSL | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | ESN | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0199 | AFR | ESN | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | ESN | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0277 | AFR | ESN | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0178 | AFR | ESN | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | ESN | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG03209 | hp1 | a0007 | c0011 | t0001 | g0067 | AFR | MSL | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0281 | AFR | MSL | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0278 | AFR | MSL | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | MSL | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG03239 | hp1 | a0003 | c0003 | t0001 | g0006 | SAS | PJL | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0122 | SAS | PJL | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | MSL | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0243 | AFR | MSL | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0219 | AFR | MSL | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG03486 | hp2 | a0002 | c0002 | t0001 | g0050 | AFR | MSL | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0049 | SAS | PJL | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0106 | SAS | PJL | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0058 | SAS | PJL | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0048 | SAS | PJL | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0058 | SAS | PJL | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0049 | SAS | PJL | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0007 | AFR | ESN | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0090 | AFR | ESN | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0228 | AFR | GWD | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0244 | AFR | GWD | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | MSL | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0234 | AFR | MSL | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0092 | SAS | PJL | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG03654 | hp2 | a0001 | c0005 | t0001 | g0137 | SAS | PJL | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0124 | SAS | PJL | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0054 | SAS | PJL | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0128 | SAS | STU | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0214 | SAS | STU | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0131 | SAS | PJL | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG03704 | hp2 | a0001 | c0001 | t0005 | g0284 | SAS | PJL | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG03710 | hp1 | a0003 | c0003 | t0001 | g0006 | SAS | PJL | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG03831 | hp1 | a0001 | c0005 | t0001 | g0138 | SAS | BEB | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0237 | SAS | BEB | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0017 | SAS | BEB | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG03834 | hp2 | a0002 | c0002 | t0002 | g0282 | SAS | BEB | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0084 | SAS | BEB | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0127 | SAS | STU | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0112 | SAS | STU | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0121 | SAS | BEB | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0226 | SAS | BEB | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0265 | SAS | STU | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0030 | SAS | STU | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0120 | SAS | STU | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0189 | SAS | STU | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0070 | SAS | STU | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0004 | SAS | STU | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | YRI | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0250 | AFR | YRI | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | CHB | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0258 | EAS | CHB | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | CHB | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0154 | EAS | CHB | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | YRI | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0232 | AFR | YRI | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0099 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0163 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0117 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0267 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0114 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0257 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0183 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0155 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0256 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0251 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA18988 | hp2 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0252 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA18997 | hp1 | a0001 | c0001 | t0002 | g0197 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA19001 | hp1 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0246 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0220 | AFR | LWK | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | LWK | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA19043 | hp1 | a0008 | c0006 | t0001 | g0236 | AFR | LWK | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0206 | AFR | LWK | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0168 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0270 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA19078 | hp2 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0158 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA19083 | hp2 | a0001 | c0001 | t0002 | g0173 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | YRI | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | YRI | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0274 | AFR | ASW | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA20129 | hp2 | a0002 | c0002 | t0001 | g0280 | AFR | ASW | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0012 | EUR | TSI | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0036 | EUR | TSI | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0019 | EUR | TSI | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0104 | EUR | TSI | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0160 | SAS | GIH | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0087 | SAS | GIH | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0011 | AMR | CLM | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0210 | AMR | CLM | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | ACB | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0227 | AFR | ACB | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0177 | AFR | ACB | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG02486 | hp2 | a0001 | c0004 | t0001 | g0024 | AFR | ACB | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0181 | AFR | ACB | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0204 | AFR | ACB | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0205 | AFR | MSL | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | MSL | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG06807 | hp1 | a0001 | c0004 | t0001 | g0024 | AFR | USA | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0264 | AFR | USA | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0027 | AFR | USA | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0203 | AFR | USA | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA21309 | hp1 | a0009 | c0007 | t0002 | g0180 | AFR | LWK | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | LWK | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0134 | REF | REF | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| homoSapiens | grch38p0 | a0003 | c0003 | t0001 | g0006 | REF | REF | C8B_chr1_56924207_56971015 | C8B | chr1 | 56924207 | 56971015 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:56945851 | C | T | 1 | a0008 | 1 | NA19043.hp1 | missense_variant | MODERATE | c.1075G>A | p.Val359Ile | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 7/12 | 1142/2040 | 1075/1776 | 359/591 | chr1 | 56945851 | |||
| chr1:56945914 | G | A | 1 | a0009 | 1 | NA21309.hp1 | missense_variant | MODERATE | c.1012C>T | p.Arg338Cys | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 7/12 | 1079/2040 | 1012/1776 | 338/591 | chr1 | 56945914 | |||
| chr1:56946018 | T | C | 1 | a0005 | 1 | HG02683.hp2 | missense_variant | MODERATE | c.908A>G | p.His303Arg | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 7/12 | 975/2040 | 908/1776 | 303/591 | chr1 | 56946018 | |||
| chr1:56949590 | G | C | 1 | a0006 | 1 | HG02976.hp2 | missense_variant | MODERATE | c.829C>G | p.His277Asp | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 6/12 | 896/2040 | 829/1776 | 277/591 | chr1 | 56949590 | |||
| chr1:56949637 | G | A | 1 | a0002 | 8 | HG01070.hp1 HG01192.hp1 HG01891.hp1 others(5): Show |
missense_variant | MODERATE | c.782C>T | p.Pro261Leu | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 6/12 | 849/2040 | 782/1776 | 261/591 | chr1 | 56949637 | |||
| chr1:56952109 | G | A | 1 | a0004 | 1 | HG00621.hp2 | missense_variant | MODERATE | c.605C>T | p.Pro202Leu | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 5/12 | 672/2040 | 605/1776 | 202/591 | chr1 | 56952109 | |||
| chr1:56956811 | C | T | 8 | a0001 a0002 a0004 others(5): Show |
395 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(392): Show |
missense_variant | MODERATE | c.349G>A | p.Gly117Arg | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 3/12 | 416/2040 | 349/1776 | 117/591 | chr1 | 56956811 | |||
| chr1:56956838 | C | T | 1 | a0002 | 8 | HG01070.hp1 HG01192.hp1 HG01891.hp1 others(5): Show |
missense_variant | MODERATE | c.322G>A | p.Glu108Lys | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 3/12 | 389/2040 | 322/1776 | 108/591 | chr1 | 56956838 | |||
| chr1:56960137 | G | C | 1 | a0007 | 1 | HG03209.hp1 | missense_variant | MODERATE | c.132C>G | p.Asn44Lys | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 2/12 | 199/2040 | 132/1776 | 44/591 | chr1 | 56960137 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:56940960 | T | G | 1 | a0001c0004 | 4 | HG01243.hp1 HG02486.hp2 HG02809.hp1 others(1): Show |
synonymous_variant | LOW | c.1287A>C | p.Gly429Gly | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/12 | 1354/2040 | 1287/1776 | 429/591 | chr1 | 56940960 | |||
| chr1:56956884 | G | A | 1 | a0001c0005 | 2 | HG03654.hp2 HG03831.hp1 |
synonymous_variant | LOW | c.276C>T | p.Pro92Pro | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 3/12 | 343/2040 | 276/1776 | 92/591 | chr1 | 56956884 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:56929239 | T | A | 1 | a0001c0001t0004 | 1 | HG02735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*165A>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 12/12 | 165 | chr1 | 56929239 | ||||||
| chr1:56929318 | G | T | 1 | a0001c0001t0003 | 2 | HG00423.hp2 HG01517.hp1 |
3_prime_UTR_variant | MODIFIER | c.*86C>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 12/12 | 86 | chr1 | 56929318 | ||||||
| chr1:56929320 | T | G | 1 | a0001c0001t0003 | 2 | HG00423.hp2 HG01517.hp1 |
3_prime_UTR_variant | MODIFIER | c.*84A>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 12/12 | 84 | chr1 | 56929320 | ||||||
| chr1:56929347 | A | G | 4 | a0001c0001t0002 a0002c0002t0002 a0003c0003t0002 others(1): Show |
132 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(129): Show |
3_prime_UTR_variant | MODIFIER | c.*57T>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 12/12 | 57 | chr1 | 56929347 | ||||||
| chr1:56966011 | G | A | 1 | a0001c0001t0005 | 1 | HG03704.hp2 | 5_prime_UTR_variant | MODIFIER | c.-63C>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/12 | 63 | chr1 | 56966011 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:56929578 | T | C | 235 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(232): Show |
333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.1622-20A>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 11/11 | chr1 | 56929578 | |||||||
| chr1:56929621 | G | A | 1 | a0001c0001t0001g0031 | 2 | HG00323.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.1622-63C>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 11/11 | chr1 | 56929621 | |||||||
| chr1:56929648 | C | T | 18 | a0001c0001t0001g0014 a0001c0001t0001g0054 a0001c0001t0001g0063 others(15): Show |
22 | HG02145.hp1 HG02145.hp2 HG02486.hp1 others(19): Show |
intron_variant | MODIFIER | c.1622-90G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 11/11 | chr1 | 56929648 | |||||||
| chr1:56929748 | C | G | 90 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0005 others(87): Show |
131 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(128): Show |
intron_variant | MODIFIER | c.1622-190G>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 11/11 | chr1 | 56929748 | |||||||
| chr1:56929761 | C | G | 58 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(55): Show |
94 | HG00438.hp2 HG00609.hp1 HG00621.hp2 others(91): Show |
intron_variant | MODIFIER | c.1622-203G>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 11/11 | chr1 | 56929761 | |||||||
| chr1:56929780 | C | A | 1 | a0007c0011t0001g0067 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1622-222G>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 11/11 | chr1 | 56929780 | |||||||
| chr1:56929827 | T | C | 2 | a0001c0001t0002g0118 a0001c0001t0002g0227 |
2 | HG00099.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.1622-269A>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 11/11 | chr1 | 56929827 | |||||||
| chr1:56929865 | T | A | 15 | a0001c0001t0001g0003 a0001c0001t0001g0031 a0001c0001t0001g0045 others(12): Show |
23 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(20): Show |
intron_variant | MODIFIER | c.1622-307A>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 11/11 | chr1 | 56929865 | |||||||
| chr1:56929919 | G | C | 91 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0005 others(88): Show |
132 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.1622-361C>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 11/11 | chr1 | 56929919 | |||||||
| chr1:56930012 | T | G | 91 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0005 others(88): Show |
132 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.1622-454A>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 11/11 | chr1 | 56930012 | |||||||
| chr1:56930028 | G | A | 91 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0005 others(88): Show |
132 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.1622-470C>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 11/11 | chr1 | 56930028 | |||||||
| chr1:56930032 | C | A | 1 | a0002c0002t0001g0223 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1622-474G>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 11/11 | chr1 | 56930032 | |||||||
| chr1:56930045 | C | A | 1 | a0001c0001t0002g0265 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1622-487G>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 11/11 | chr1 | 56930045 | |||||||
| chr1:56930077 | G | C | 91 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0005 others(88): Show |
132 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.1622-519C>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 11/11 | chr1 | 56930077 | |||||||
| chr1:56930341 | A | G | 91 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0005 others(88): Show |
132 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.1622-783T>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 11/11 | chr1 | 56930341 | |||||||
| chr1:56930603 | C | T | 109 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(106): Show |
156 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(153): Show |
intron_variant | MODIFIER | c.1622-1045G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 11/11 | chr1 | 56930603 | |||||||
| chr1:56930780 | A | G | 6 | a0001c0001t0001g0008 a0001c0001t0001g0095 a0001c0001t0001g0191 others(3): Show |
10 | HG02071.hp2 NA18947.hp1 NA18960.hp1 others(7): Show |
intron_variant | MODIFIER | c.1621+1030T>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 11/11 | chr1 | 56930780 | |||||||
| chr1:56930869 | C | T | 95 | a0001c0001t0001g0023 a0001c0001t0001g0077 a0001c0001t0001g0170 others(92): Show |
138 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.1621+941G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 11/11 | chr1 | 56930869 | |||||||
| chr1:56930894 | C | T | 1 | a0001c0001t0001g0100 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1621+916G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 11/11 | chr1 | 56930894 | |||||||
| chr1:56930896 | A | G | 1 | a0001c0001t0001g0061 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1621+914T>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 11/11 | chr1 | 56930896 | |||||||
| chr1:56930977 | G | A | 1 | a0001c0001t0002g0257 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1621+833C>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 11/11 | chr1 | 56930977 | |||||||
| chr1:56931020 | A | C | 1 | a0001c0001t0001g0068 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1621+790T>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 11/11 | chr1 | 56931020 | |||||||
| chr1:56931366 | A | G | 91 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0005 others(88): Show |
132 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.1621+444T>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 11/11 | chr1 | 56931366 | |||||||
| chr1:56931409 | C | T | 90 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0005 others(87): Show |
131 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(128): Show |
intron_variant | MODIFIER | c.1621+401G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 11/11 | chr1 | 56931409 | |||||||
| chr1:56931410 | G | T | 1 | a0001c0001t0002g0182 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1621+400C>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 11/11 | chr1 | 56931410 | |||||||
| chr1:56931443 | T | C | 1 | a0007c0011t0001g0067 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1621+367A>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 11/11 | chr1 | 56931443 | |||||||
| chr1:56931510 | T | C | 91 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0005 others(88): Show |
132 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.1621+300A>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 11/11 | chr1 | 56931510 | |||||||
| chr1:56931628 | G | A | 91 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0005 others(88): Show |
132 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.1621+182C>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 11/11 | chr1 | 56931628 | |||||||
| chr1:56931679 | C | T | 1 | a0001c0001t0002g0256 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1621+131G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 11/11 | chr1 | 56931679 | |||||||
| chr1:56931771 | C | A | 12 | a0001c0001t0001g0014 a0001c0001t0001g0063 a0001c0001t0001g0085 others(9): Show |
15 | HG02145.hp2 HG02486.hp1 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.1621+39G>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 11/11 | chr1 | 56931771 | |||||||
| chr1:56931900 | AGT | A | 3 | a0001c0001t0001g0095 a0001c0001t0001g0193 a0001c0001t0001g0200 |
3 | HG02071.hp2 NA18990.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.1553-24_1553-23del others(2): Show |
C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 10/11 | chr1 | 56931900 | |||||||
| chr1:56931969 | G | T | 10 | a0001c0001t0001g0069 a0001c0001t0001g0171 a0001c0001t0001g0178 others(7): Show |
11 | HG01255.hp1 HG01891.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.1553-91C>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 10/11 | chr1 | 56931969 | |||||||
| chr1:56932014 | G | A | 1 | a0001c0001t0001g0278 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1553-136C>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 10/11 | chr1 | 56932014 | |||||||
| chr1:56932060 | C | T | 3 | a0001c0001t0001g0116 a0001c0005t0001g0137 a0001c0005t0001g0138 |
3 | HG02145.hp1 HG03654.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.1553-182G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 10/11 | chr1 | 56932060 | |||||||
| chr1:56932065 | G | C | 91 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0005 others(88): Show |
132 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.1553-187C>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 10/11 | chr1 | 56932065 | |||||||
| chr1:56932153 | A | G | 1 | a0001c0001t0001g0204 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1553-275T>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 10/11 | chr1 | 56932153 | |||||||
| chr1:56932174 | A | G | 3 | a0001c0001t0001g0063 a0001c0001t0001g0177 a0001c0001t0001g0274 |
3 | HG02145.hp2 HG02486.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1553-296T>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 10/11 | chr1 | 56932174 | |||||||
| chr1:56932259 | C | A | 2 | a0001c0001t0002g0118 a0001c0001t0002g0227 |
2 | HG00099.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.1553-381G>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 10/11 | chr1 | 56932259 | |||||||
| chr1:56932594 | C | T | 15 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0171 others(12): Show |
17 | HG01243.hp1 HG01255.hp1 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.1553-716G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 10/11 | chr1 | 56932594 | |||||||
| chr1:56932615 | T | C | 1 | a0001c0001t0001g0219 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1552+720A>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 10/11 | chr1 | 56932615 | |||||||
| chr1:56932658 | C | T | 1 | a0001c0001t0001g0185 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1552+677G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 10/11 | chr1 | 56932658 | |||||||
| chr1:56932705 | C | T | 92 | a0001c0001t0001g0052 a0001c0001t0002g0002 a0001c0001t0002g0004 others(89): Show |
134 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(131): Show |
intron_variant | MODIFIER | c.1552+630G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 10/11 | chr1 | 56932705 | |||||||
| chr1:56932768 | G | A | 1 | a0001c0001t0001g0262 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1552+567C>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 10/11 | chr1 | 56932768 | |||||||
| chr1:56933000 | C | T | 1 | a0001c0001t0001g0278 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1552+335G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 10/11 | chr1 | 56933000 | |||||||
| chr1:56933029 | G | A | 1 | a0001c0001t0002g0038 | 2 | NA18950.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.1552+306C>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 10/11 | chr1 | 56933029 | |||||||
| chr1:56933525 | A | C | 1 | a0001c0001t0002g0182 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1399-37T>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56933525 | |||||||
| chr1:56933562 | G | A | 1 | a0001c0001t0001g0184 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1399-74C>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56933562 | |||||||
| chr1:56933577 | C | T | 3 | a0001c0001t0001g0116 a0001c0005t0001g0137 a0001c0005t0001g0138 |
3 | HG02145.hp1 HG03654.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.1399-89G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56933577 | |||||||
| chr1:56933776 | G | A | 1 | a0001c0001t0001g0070 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1399-288C>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56933776 | |||||||
| chr1:56933863 | G | T | 91 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0005 others(88): Show |
132 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.1399-375C>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56933863 | |||||||
| chr1:56933949 | T | C | 251 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(248): Show |
351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.1399-461A>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56933949 | |||||||
| chr1:56934140 | CTTT | C | 108 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(105): Show |
154 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.1399-655_1399-653d others(5): Show |
C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56934140 | |||||||
| chr1:56934142 | T | C | 3 | a0001c0001t0001g0063 a0001c0001t0001g0177 a0001c0001t0001g0274 |
3 | HG02145.hp2 HG02486.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1399-654A>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56934142 | |||||||
| chr1:56934164 | C | CT | 252 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(249): Show |
352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
intron_variant | MODIFIER | c.1399-677dupA | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56934164 | |||||||
| chr1:56934168 | T | TA | 3 | a0001c0001t0001g0181 a0002c0002t0001g0176 a0002c0002t0001g0223 |
3 | HG01192.hp1 HG02280.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.1399-681_1399-680i others(3): Show |
C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56934168 | |||||||
| chr1:56934214 | A | G | 1 | a0003c0003t0002g0235 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1399-726T>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56934214 | |||||||
| chr1:56934234 | C | T | 12 | a0001c0001t0001g0014 a0001c0001t0001g0063 a0001c0001t0001g0085 others(9): Show |
15 | HG02145.hp2 HG02486.hp1 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.1399-746G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56934234 | |||||||
| chr1:56934246 | C | A | 1 | a0001c0001t0001g0249 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1399-758G>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56934246 | |||||||
| chr1:56934253 | T | A | 92 | a0001c0001t0001g0052 a0001c0001t0002g0002 a0001c0001t0002g0004 others(89): Show |
134 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(131): Show |
intron_variant | MODIFIER | c.1399-765A>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56934253 | |||||||
| chr1:56934405 | G | A | 18 | a0001c0001t0001g0014 a0001c0001t0001g0054 a0001c0001t0001g0063 others(15): Show |
22 | HG02145.hp1 HG02145.hp2 HG02486.hp1 others(19): Show |
intron_variant | MODIFIER | c.1399-917C>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56934405 | |||||||
| chr1:56934462 | A | G | 1 | a0007c0011t0001g0067 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1399-974T>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56934462 | |||||||
| chr1:56934564 | C | T | 1 | a0001c0001t0001g0278 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1399-1076G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56934564 | |||||||
| chr1:56934587 | C | T | 3 | a0001c0001t0001g0057 a0001c0001t0001g0131 a0001c0001t0001g0276 |
4 | HG02257.hp2 HG02280.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.1399-1099G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56934587 | |||||||
| chr1:56934588 | G | A | 15 | a0001c0001t0001g0003 a0001c0001t0001g0031 a0001c0001t0001g0045 others(12): Show |
23 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(20): Show |
intron_variant | MODIFIER | c.1399-1100C>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56934588 | |||||||
| chr1:56934629 | G | C | 1 | a0001c0001t0001g0145 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1399-1141C>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56934629 | |||||||
| chr1:56934902 | A | C | 235 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(232): Show |
333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.1399-1414T>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56934902 | |||||||
| chr1:56934997 | G | A | 4 | a0001c0001t0001g0277 a0001c0004t0001g0024 a0001c0004t0001g0153 others(1): Show |
5 | HG01243.hp1 HG02486.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1399-1509C>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56934997 | |||||||
| chr1:56935311 | C | T | 23 | a0001c0001t0001g0030 a0001c0001t0001g0082 a0001c0001t0001g0084 others(20): Show |
25 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(22): Show |
intron_variant | MODIFIER | c.1399-1823G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56935311 | |||||||
| chr1:56935338 | T | A | 1 | a0001c0001t0001g0273 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1399-1850A>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56935338 | |||||||
| chr1:56935348 | C | T | 19 | a0001c0001t0002g0042 a0001c0001t0002g0060 a0001c0001t0002g0080 others(16): Show |
20 | HG00544.hp2 HG00597.hp1 HG00597.hp2 others(17): Show |
intron_variant | MODIFIER | c.1399-1860G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56935348 | |||||||
| chr1:56935375 | C | T | 3 | a0001c0001t0002g0090 a0001c0001t0002g0091 a0001c0001t0002g0147 |
3 | HG00639.hp2 HG01884.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1399-1887G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56935375 | |||||||
| chr1:56935437 | C | A | 15 | a0001c0001t0001g0003 a0001c0001t0001g0031 a0001c0001t0001g0045 others(12): Show |
23 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(20): Show |
intron_variant | MODIFIER | c.1399-1949G>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56935437 | |||||||
| chr1:56935442 | C | G | 3 | a0001c0001t0001g0054 a0001c0001t0001g0070 a0005c0008t0001g0268 |
4 | HG02683.hp2 HG02735.hp1 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.1399-1954G>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56935442 | |||||||
| chr1:56936058 | G | T | 1 | a0001c0001t0001g0277 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1399-2570C>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56936058 | |||||||
| chr1:56936096 | A | C | 1 | a0001c0001t0001g0132 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1399-2608T>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56936096 | |||||||
| chr1:56936245 | A | G | 6 | a0001c0001t0001g0054 a0001c0001t0001g0070 a0001c0001t0001g0116 others(3): Show |
7 | HG02145.hp1 HG02683.hp2 HG02735.hp1 others(4): Show |
intron_variant | MODIFIER | c.1399-2757T>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56936245 | |||||||
| chr1:56936306 | A | T | 2 | a0001c0001t0002g0118 a0001c0001t0002g0227 |
2 | HG00099.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.1399-2818T>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56936306 | |||||||
| chr1:56936309 | T | C | 276 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(273): Show |
385 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(382): Show |
intron_variant | MODIFIER | c.1399-2821A>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56936309 | |||||||
| chr1:56936319 | T | C | 1 | a0001c0001t0001g0123 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.1399-2831A>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56936319 | |||||||
| chr1:56936511 | TA | T | 74 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0005 others(71): Show |
115 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.1399-3024delT | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56936511 | |||||||
| chr1:56936513 | AAT | A | 6 | a0001c0001t0001g0052 a0001c0001t0002g0073 a0001c0001t0002g0122 others(3): Show |
7 | HG01515.hp2 HG03098.hp2 HG03239.hp2 others(4): Show |
intron_variant | MODIFIER | c.1399-3027_1399-302 others(6): Show |
C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56936513 | |||||||
| chr1:56936514 | A | T | 10 | a0001c0001t0002g0060 a0001c0001t0002g0075 a0001c0001t0002g0090 others(7): Show |
10 | HG00099.hp2 HG01106.hp2 HG02027.hp2 others(7): Show |
intron_variant | MODIFIER | c.1399-3026T>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56936514 | |||||||
| chr1:56936514 | AT | A | 102 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(99): Show |
139 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.1399-3027delA | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56936514 | |||||||
| chr1:56936514 | ATT | A | 33 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0025 others(30): Show |
41 | HG01109.hp1 HG01109.hp2 HG01168.hp2 others(38): Show |
intron_variant | MODIFIER | c.1399-3028_1399-302 others(6): Show |
C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56936514 | |||||||
| chr1:56936601 | C | CT | 23 | a0001c0001t0001g0014 a0001c0001t0001g0093 a0001c0001t0001g0150 others(20): Show |
28 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(25): Show |
intron_variant | MODIFIER | c.1399-3114dupA | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56936601 | |||||||
| chr1:56936605 | T | A | 1 | a0002c0002t0001g0176 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1399-3117A>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56936605 | |||||||
| chr1:56936697 | C | T | 4 | a0001c0001t0001g0277 a0001c0004t0001g0024 a0001c0004t0001g0153 others(1): Show |
5 | HG01243.hp1 HG02486.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1399-3209G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56936697 | |||||||
| chr1:56936974 | T | G | 3 | a0001c0001t0001g0063 a0001c0001t0001g0177 a0001c0001t0001g0274 |
3 | HG02145.hp2 HG02486.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1399-3486A>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56936974 | |||||||
| chr1:56937126 | G | C | 1 | a0001c0001t0002g0119 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1399-3638C>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56937126 | |||||||
| chr1:56937223 | C | T | 2 | a0001c0001t0002g0096 a0001c0001t0002g0117 |
2 | NA18948.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.1398+3626G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56937223 | |||||||
| chr1:56937289 | C | T | 1 | a0009c0007t0002g0180 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1398+3560G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56937289 | |||||||
| chr1:56937488 | T | C | 3 | a0001c0001t0001g0032 a0001c0001t0001g0056 a0001c0001t0001g0089 |
5 | NA18945.hp2 NA18946.hp2 NA18954.hp1 others(2): Show |
intron_variant | MODIFIER | c.1398+3361A>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56937488 | |||||||
| chr1:56937674 | ATT | A | 10 | a0001c0001t0001g0069 a0001c0001t0001g0171 a0001c0001t0001g0178 others(7): Show |
11 | HG01255.hp1 HG01891.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.1398+3173_1398+317 others(6): Show |
C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56937674 | |||||||
| chr1:56937677 | T | A | 10 | a0001c0001t0001g0069 a0001c0001t0001g0171 a0001c0001t0001g0178 others(7): Show |
11 | HG01255.hp1 HG01891.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.1398+3172A>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56937677 | |||||||
| chr1:56937763 | AT | A | 32 | a0001c0001t0001g0026 a0001c0001t0001g0034 a0001c0001t0001g0035 others(29): Show |
40 | HG01109.hp1 HG01109.hp2 HG01243.hp1 others(37): Show |
intron_variant | MODIFIER | c.1398+3085delA | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56937763 | |||||||
| chr1:56937981 | T | C | 2 | a0001c0001t0001g0097 a0001c0001t0001g0098 |
2 | HG01978.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.1398+2868A>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56937981 | |||||||
| chr1:56938130 | C | G | 91 | a0001c0001t0001g0052 a0001c0001t0002g0002 a0001c0001t0002g0004 others(88): Show |
133 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(130): Show |
intron_variant | MODIFIER | c.1398+2719G>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56938130 | |||||||
| chr1:56938137 | T | C | 1 | a0001c0001t0001g0026 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1398+2712A>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56938137 | |||||||
| chr1:56938226 | A | G | 1 | a0001c0001t0001g0055 | 2 | HG02155.hp1 NA18948.hp2 |
intron_variant | MODIFIER | c.1398+2623T>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56938226 | |||||||
| chr1:56938254 | T | C | 1 | a0001c0001t0001g0185 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1398+2595A>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56938254 | |||||||
| chr1:56938322 | T | C | 1 | a0001c0001t0001g0220 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1398+2527A>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56938322 | |||||||
| chr1:56938428 | A | C | 2 | a0001c0001t0003g0051 a0002c0002t0001g0283 |
3 | HG00423.hp2 HG01070.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1398+2421T>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56938428 | |||||||
| chr1:56938716 | T | C | 1 | a0001c0001t0002g0163 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1398+2133A>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56938716 | |||||||
| chr1:56938828 | T | C | 1 | a0001c0001t0001g0174 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1398+2021A>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56938828 | |||||||
| chr1:56938891 | G | GA | 90 | a0001c0001t0001g0052 a0001c0001t0002g0002 a0001c0001t0002g0004 others(87): Show |
132 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.1398+1957dupT | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56938891 | |||||||
| chr1:56939066 | C | T | 250 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(247): Show |
350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.1398+1783G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56939066 | |||||||
| chr1:56939222 | C | T | 3 | a0001c0001t0001g0062 a0001c0001t0001g0065 a0001c0001t0001g0066 |
3 | HG02895.hp2 HG02897.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1398+1627G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56939222 | |||||||
| chr1:56939232 | T | C | 1 | a0001c0001t0001g0061 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1398+1617A>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56939232 | |||||||
| chr1:56939285 | G | T | 1 | a0001c0001t0001g0052 | 2 | HG03098.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1398+1564C>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56939285 | |||||||
| chr1:56939422 | A | T | 1 | a0001c0001t0001g0068 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1398+1427T>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56939422 | |||||||
| chr1:56939550 | A | T | 90 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0005 others(87): Show |
131 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(128): Show |
intron_variant | MODIFIER | c.1398+1299T>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56939550 | |||||||
| chr1:56939583 | A | G | 1 | a0001c0001t0001g0079 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1398+1266T>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56939583 | |||||||
| chr1:56939631 | C | T | 1 | a0009c0007t0002g0180 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1398+1218G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56939631 | |||||||
| chr1:56939676 | T | C | 6 | a0001c0001t0001g0054 a0001c0001t0001g0070 a0001c0001t0001g0116 others(3): Show |
7 | HG02145.hp1 HG02683.hp2 HG02735.hp1 others(4): Show |
intron_variant | MODIFIER | c.1398+1173A>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56939676 | |||||||
| chr1:56939952 | G | A | 1 | a0001c0001t0001g0188 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1398+897C>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56939952 | |||||||
| chr1:56940015 | CGT | C | 232 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(229): Show |
329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.1398+832_1398+833d others(4): Show |
C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56940015 | |||||||
| chr1:56940030 | G | C | 1 | a0001c0001t0002g0091 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1398+819C>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56940030 | |||||||
| chr1:56940048 | C | T | 107 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(104): Show |
153 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.1398+801G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56940048 | |||||||
| chr1:56940111 | G | A | 1 | a0001c0001t0002g0058 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1398+738C>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56940111 | |||||||
| chr1:56940132 | T | G | 4 | a0001c0001t0002g0120 a0001c0001t0002g0121 a0001c0001t0002g0122 others(1): Show |
4 | HG03239.hp2 HG04184.hp1 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.1398+717A>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56940132 | |||||||
| chr1:56940399 | TA | T | 11 | a0001c0001t0001g0014 a0001c0001t0001g0065 a0001c0001t0001g0093 others(8): Show |
14 | HG00639.hp2 HG01257.hp2 HG01943.hp1 others(11): Show |
intron_variant | MODIFIER | c.1398+449delT | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56940399 | |||||||
| chr1:56940500 | T | A | 1 | a0007c0011t0001g0067 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1398+349A>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56940500 | |||||||
| chr1:56940536 | C | T | 1 | a0001c0004t0001g0024 | 2 | HG02486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1398+313G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56940536 | |||||||
| chr1:56940537 | C | T | 3 | a0001c0001t0001g0171 a0001c0001t0001g0204 a0001c0001t0001g0250 |
3 | HG02559.hp2 HG02615.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1398+312G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56940537 | |||||||
| chr1:56940538 | C | A | 13 | a0001c0001t0001g0025 a0001c0001t0001g0061 a0001c0001t0001g0062 others(10): Show |
14 | HG02622.hp1 HG02647.hp2 HG02717.hp1 others(11): Show |
intron_variant | MODIFIER | c.1398+311G>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56940538 | |||||||
| chr1:56940541 | A | T | 13 | a0001c0001t0001g0014 a0001c0001t0001g0063 a0001c0001t0001g0085 others(10): Show |
16 | HG02145.hp2 HG02486.hp1 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.1398+308T>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56940541 | |||||||
| chr1:56940574 | A | AAAG | 235 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(232): Show |
333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.1398+272_1398+274d others(5): Show |
C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56940574 | |||||||
| chr1:56940719 | T | C | 108 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(105): Show |
154 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.1398+130A>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56940719 | |||||||
| chr1:56940840 | G | A | 2 | a0001c0001t0001g0211 a0001c0001t0001g0221 |
2 | HG02886.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.1398+9C>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 9/11 | chr1 | 56940840 | |||||||
| chr1:56941157 | A | G | 1 | a0001c0001t0001g0068 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1235-145T>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 8/11 | chr1 | 56941157 | |||||||
| chr1:56941193 | C | T | 3 | a0001c0001t0001g0116 a0001c0005t0001g0137 a0001c0005t0001g0138 |
3 | HG02145.hp1 HG03654.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.1235-181G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 8/11 | chr1 | 56941193 | |||||||
| chr1:56941254 | T | C | 90 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0005 others(87): Show |
131 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(128): Show |
intron_variant | MODIFIER | c.1235-242A>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 8/11 | chr1 | 56941254 | |||||||
| chr1:56941308 | A | T | 1 | a0001c0001t0002g0087 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1235-296T>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 8/11 | chr1 | 56941308 | |||||||
| chr1:56941494 | GTAGA | G | 10 | a0001c0001t0001g0034 a0001c0001t0001g0041 a0001c0001t0001g0046 others(7): Show |
14 | HG01109.hp1 HG01109.hp2 HG01346.hp2 others(11): Show |
intron_variant | MODIFIER | c.1235-486_1235-483d others(6): Show |
C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 8/11 | chr1 | 56941494 | |||||||
| chr1:56941494 | GTAGATAG others(9): Show |
G | 75 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0010 others(72): Show |
108 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.1235-498_1235-483d others(18): Show |
C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 8/11 | chr1 | 56941494 | |||||||
| chr1:56941494 | GTAGATAG others(13): Show |
G | 20 | a0001c0001t0001g0025 a0001c0001t0001g0039 a0001c0001t0001g0104 others(17): Show |
23 | HG00099.hp1 HG00423.hp2 HG00621.hp2 others(20): Show |
intron_variant | MODIFIER | c.1235-502_1235-483d others(22): Show |
C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 8/11 | chr1 | 56941494 | |||||||
| chr1:56941494 | GTAGATAG others(17): Show |
G | 14 | a0001c0001t0001g0003 a0001c0001t0001g0031 a0001c0001t0001g0045 others(11): Show |
22 | HG00323.hp1 HG00408.hp1 HG00738.hp1 others(19): Show |
intron_variant | MODIFIER | c.1235-506_1235-483d others(26): Show |
C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 8/11 | chr1 | 56941494 | |||||||
| chr1:56941494 | GTAGATAG others(21): Show |
G | 4 | a0001c0001t0001g0116 a0001c0001t0001g0186 a0001c0005t0001g0137 others(1): Show |
4 | HG02055.hp2 HG02145.hp1 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.1235-510_1235-483d others(30): Show |
C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 8/11 | chr1 | 56941494 | |||||||
| chr1:56941494 | GTAGATAG others(25): Show |
G | 1 | a0001c0001t0001g0149 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1235-514_1235-483d others(34): Show |
C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 8/11 | chr1 | 56941494 | |||||||
| chr1:56941497 | GATAGATA others(5): Show |
G | 13 | a0001c0001t0001g0009 a0001c0001t0001g0029 a0001c0001t0001g0053 others(10): Show |
18 | HG00609.hp1 HG00733.hp1 HG00735.hp2 others(15): Show |
intron_variant | MODIFIER | c.1235-497_1235-486d others(14): Show |
C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 8/11 | chr1 | 56941497 | |||||||
| chr1:56941501 | GATAGATA others(1): Show |
G | 3 | a0001c0001t0001g0009 a0001c0001t0001g0035 a0001c0001t0001g0100 |
4 | HG02451.hp1 HG02647.hp1 NA18965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1235-497_1235-490d others(10): Show |
C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 8/11 | chr1 | 56941501 | |||||||
| chr1:56941505 | G | C | 2 | a0001c0001t0001g0132 a0001c0001t0001g0179 |
2 | HG02257.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.1235-493C>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 8/11 | chr1 | 56941505 | |||||||
| chr1:56941509 | C | CATAG | 31 | a0001c0001t0001g0221 a0001c0001t0001g0271 a0001c0001t0002g0002 others(28): Show |
39 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(36): Show |
intron_variant | MODIFIER | c.1235-501_1235-498d others(6): Show |
C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 8/11 | chr1 | 56941509 | |||||||
| chr1:56941509 | C | CATAGATA others(1): Show |
9 | a0001c0001t0001g0052 a0001c0001t0001g0142 a0001c0001t0001g0211 others(6): Show |
11 | HG00544.hp2 HG00639.hp1 HG01123.hp1 others(8): Show |
intron_variant | MODIFIER | c.1235-505_1235-498d others(10): Show |
C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 8/11 | chr1 | 56941509 | |||||||
| chr1:56941509 | C | G | 2 | a0001c0001t0001g0132 a0001c0001t0001g0179 |
2 | HG02257.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.1235-497G>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 8/11 | chr1 | 56941509 | |||||||
| chr1:56941509 | CATAG | C | 32 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(29): Show |
47 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(44): Show |
intron_variant | MODIFIER | c.1235-501_1235-498d others(6): Show |
C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 8/11 | chr1 | 56941509 | |||||||
| chr1:56941509 | CATAGATA others(1): Show |
C | 6 | a0001c0001t0001g0103 a0001c0001t0001g0110 a0001c0001t0001g0199 others(3): Show |
6 | HG00639.hp2 HG00642.hp1 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.1235-505_1235-498d others(10): Show |
C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 8/11 | chr1 | 56941509 | |||||||
| chr1:56941509 | CATAGATA others(13): Show |
C | 16 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0171 others(13): Show |
18 | HG01243.hp1 HG01255.hp1 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.1235-517_1235-498d others(22): Show |
C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 8/11 | chr1 | 56941509 | |||||||
| chr1:56941513 | G | C | 1 | a0001c0001t0001g0035 | 2 | HG02451.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1235-501C>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 8/11 | chr1 | 56941513 | |||||||
| chr1:56941548 | A | G | 2 | a0001c0001t0001g0012 a0001c0001t0001g0190 |
5 | HG00735.hp2 HG01074.hp2 HG01081.hp2 others(2): Show |
intron_variant | MODIFIER | c.1235-536T>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 8/11 | chr1 | 56941548 | |||||||
| chr1:56941725 | A | T | 13 | a0001c0001t0001g0014 a0001c0001t0001g0063 a0001c0001t0001g0085 others(10): Show |
16 | HG02145.hp2 HG02486.hp1 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.1235-713T>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 8/11 | chr1 | 56941725 | |||||||
| chr1:56941811 | C | T | 90 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0005 others(87): Show |
131 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(128): Show |
intron_variant | MODIFIER | c.1235-799G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 8/11 | chr1 | 56941811 | |||||||
| chr1:56941814 | A | G | 1 | a0001c0001t0001g0234 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1235-802T>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 8/11 | chr1 | 56941814 | |||||||
| chr1:56941963 | A | G | 1 | a0001c0001t0001g0228 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1235-951T>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 8/11 | chr1 | 56941963 | |||||||
| chr1:56942219 | T | C | 1 | a0007c0011t0001g0067 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1235-1207A>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 8/11 | chr1 | 56942219 | |||||||
| chr1:56942261 | CTAAG | C | 235 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(232): Show |
333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.1235-1253_1235-125 others(8): Show |
C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 8/11 | chr1 | 56942261 | |||||||
| chr1:56942422 | C | T | 13 | a0001c0001t0001g0025 a0001c0001t0001g0061 a0001c0001t0001g0062 others(10): Show |
14 | HG02622.hp1 HG02647.hp2 HG02717.hp1 others(11): Show |
intron_variant | MODIFIER | c.1234+1274G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 8/11 | chr1 | 56942422 | |||||||
| chr1:56942448 | T | A | 1 | a0001c0001t0001g0083 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1234+1248A>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 8/11 | chr1 | 56942448 | |||||||
| chr1:56942501 | G | A | 2 | a0001c0001t0001g0181 a0002c0002t0001g0176 |
2 | HG02280.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.1234+1195C>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 8/11 | chr1 | 56942501 | |||||||
| chr1:56942507 | G | C | 108 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(105): Show |
154 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.1234+1189C>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 8/11 | chr1 | 56942507 | |||||||
| chr1:56942519 | A | G | 19 | a0001c0001t0001g0014 a0001c0001t0001g0054 a0001c0001t0001g0063 others(16): Show |
23 | HG02145.hp1 HG02145.hp2 HG02486.hp1 others(20): Show |
intron_variant | MODIFIER | c.1234+1177T>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 8/11 | chr1 | 56942519 | |||||||
| chr1:56942551 | A | G | 19 | a0001c0001t0001g0014 a0001c0001t0001g0054 a0001c0001t0001g0063 others(16): Show |
23 | HG02145.hp1 HG02145.hp2 HG02486.hp1 others(20): Show |
intron_variant | MODIFIER | c.1234+1145T>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 8/11 | chr1 | 56942551 | |||||||
| chr1:56942566 | G | A | 1 | a0001c0001t0001g0068 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1234+1130C>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 8/11 | chr1 | 56942566 | |||||||
| chr1:56942605 | G | T | 1 | a0001c0001t0001g0188 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1234+1091C>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 8/11 | chr1 | 56942605 | |||||||
| chr1:56942634 | G | C | 1 | a0001c0001t0001g0277 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1234+1062C>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 8/11 | chr1 | 56942634 | |||||||
| chr1:56942656 | G | A | 1 | a0009c0007t0002g0180 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1234+1040C>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 8/11 | chr1 | 56942656 | |||||||
| chr1:56942668 | C | T | 2 | a0001c0001t0002g0257 a0001c0001t0002g0258 |
2 | NA18612.hp2 NA18959.hp1 |
intron_variant | MODIFIER | c.1234+1028G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 8/11 | chr1 | 56942668 | |||||||
| chr1:56942750 | C | T | 1 | a0001c0001t0002g0114 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1234+946G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 8/11 | chr1 | 56942750 | |||||||
| chr1:56942806 | A | C | 1 | a0001c0001t0001g0185 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1234+890T>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 8/11 | chr1 | 56942806 | |||||||
| chr1:56942838 | A | T | 3 | a0001c0001t0001g0171 a0001c0001t0001g0204 a0001c0001t0001g0250 |
3 | HG02559.hp2 HG02615.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1234+858T>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 8/11 | chr1 | 56942838 | |||||||
| chr1:56942964 | C | T | 1 | a0007c0011t0001g0067 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1234+732G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 8/11 | chr1 | 56942964 | |||||||
| chr1:56943052 | C | A | 2 | a0001c0001t0001g0205 a0001c0001t0001g0220 |
2 | HG03471.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1234+644G>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 8/11 | chr1 | 56943052 | |||||||
| chr1:56943361 | C | T | 243 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(240): Show |
337 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(334): Show |
intron_variant | MODIFIER | c.1234+335G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 8/11 | chr1 | 56943361 | |||||||
| chr1:56943403 | A | G | 14 | a0001c0001t0002g0042 a0001c0001t0002g0060 a0001c0001t0002g0114 others(11): Show |
15 | HG00544.hp2 HG00597.hp2 HG00621.hp1 others(12): Show |
intron_variant | MODIFIER | c.1234+293T>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 8/11 | chr1 | 56943403 | |||||||
| chr1:56943421 | A | G | 1 | a0001c0001t0002g0147 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1234+275T>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 8/11 | chr1 | 56943421 | |||||||
| chr1:56943485 | T | C | 7 | a0001c0001t0001g0083 a0001c0001t0001g0203 a0001c0001t0001g0206 others(4): Show |
7 | HG02572.hp1 HG02886.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.1234+211A>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 8/11 | chr1 | 56943485 | |||||||
| chr1:56943531 | G | A | 1 | a0001c0001t0001g0020 | 3 | HG00733.hp2 HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1234+165C>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 8/11 | chr1 | 56943531 | |||||||
| chr1:56943536 | C | T | 3 | a0001c0001t0001g0095 a0001c0001t0001g0193 a0001c0001t0001g0200 |
3 | HG02071.hp2 NA18990.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.1234+160G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 8/11 | chr1 | 56943536 | |||||||
| chr1:56943654 | T | C | 12 | a0001c0001t0001g0030 a0001c0001t0001g0082 a0001c0001t0001g0084 others(9): Show |
13 | HG00099.hp1 HG00323.hp2 HG00735.hp1 others(10): Show |
intron_variant | MODIFIER | c.1234+42A>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 8/11 | chr1 | 56943654 | |||||||
| chr1:56943656 | A | G | 4 | a0001c0001t0001g0031 a0001c0001t0001g0109 a0001c0001t0001g0148 others(1): Show |
5 | HG00323.hp1 HG01168.hp2 HG01243.hp2 others(2): Show |
intron_variant | MODIFIER | c.1234+40T>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 8/11 | chr1 | 56943656 | |||||||
| chr1:56943691 | C | G | 1 | a0001c0001t0002g0059 | 2 | HG01256.hp1 HG01258.hp2 |
splice_region_variant&intron_variant | LOW | c.1234+5G>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 8/11 | chr1 | 56943691 | |||||||
| chr1:56943911 | T | A | 6 | a0001c0001t0001g0086 a0001c0001t0001g0175 a0001c0001t0001g0222 others(3): Show |
6 | HG01361.hp1 HG02572.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1106-87A>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 7/11 | chr1 | 56943911 | |||||||
| chr1:56943932 | G | A | 6 | a0001c0001t0001g0086 a0001c0001t0001g0175 a0001c0001t0001g0222 others(3): Show |
6 | HG01361.hp1 HG02572.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1106-108C>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 7/11 | chr1 | 56943932 | |||||||
| chr1:56943989 | C | T | 3 | a0001c0001t0001g0171 a0001c0001t0001g0204 a0001c0001t0001g0250 |
3 | HG02559.hp2 HG02615.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1106-165G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 7/11 | chr1 | 56943989 | |||||||
| chr1:56944055 | G | A | 1 | a0001c0001t0001g0145 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1106-231C>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 7/11 | chr1 | 56944055 | |||||||
| chr1:56944071 | T | C | 31 | a0001c0001t0001g0014 a0001c0001t0001g0057 a0001c0001t0001g0061 others(28): Show |
37 | HG00597.hp1 HG00639.hp1 HG01243.hp1 others(34): Show |
intron_variant | MODIFIER | c.1106-247A>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 7/11 | chr1 | 56944071 | |||||||
| chr1:56944141 | C | G | 1 | a0001c0001t0002g0158 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1106-317G>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 7/11 | chr1 | 56944141 | |||||||
| chr1:56944287 | G | A | 3 | a0001c0001t0001g0171 a0001c0001t0001g0204 a0001c0001t0001g0250 |
3 | HG02559.hp2 HG02615.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1106-463C>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 7/11 | chr1 | 56944287 | |||||||
| chr1:56944340 | C | T | 9 | a0001c0001t0001g0014 a0001c0001t0001g0057 a0001c0001t0001g0061 others(6): Show |
13 | HG02257.hp2 HG02280.hp2 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.1106-516G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 7/11 | chr1 | 56944340 | |||||||
| chr1:56944369 | C | G | 7 | a0001c0001t0001g0014 a0001c0001t0001g0061 a0001c0001t0001g0093 others(4): Show |
10 | HG02615.hp1 HG02630.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.1106-545G>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 7/11 | chr1 | 56944369 | |||||||
| chr1:56944398 | T | TA | 4 | a0001c0001t0001g0171 a0001c0001t0001g0204 a0001c0001t0001g0250 others(1): Show |
4 | HG02258.hp1 HG02559.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.1106-575dupT | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 7/11 | chr1 | 56944398 | |||||||
| chr1:56944472 | A | C | 266 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(263): Show |
372 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(369): Show |
intron_variant | MODIFIER | c.1106-648T>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 7/11 | chr1 | 56944472 | |||||||
| chr1:56944598 | A | G | 1 | a0001c0001t0001g0278 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1106-774T>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 7/11 | chr1 | 56944598 | |||||||
| chr1:56944628 | C | T | 2 | a0001c0001t0001g0053 a0001c0001t0001g0254 |
3 | NA18988.hp1 NA19068.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.1106-804G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 7/11 | chr1 | 56944628 | |||||||
| chr1:56945024 | T | C | 1 | a0001c0001t0002g0163 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1105+797A>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 7/11 | chr1 | 56945024 | |||||||
| chr1:56945077 | C | A | 4 | a0001c0001t0002g0240 a0001c0001t0002g0246 a0001c0001t0002g0266 others(1): Show |
4 | HG00597.hp2 HG00621.hp1 NA18951.hp1 others(1): Show |
intron_variant | MODIFIER | c.1105+744G>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 7/11 | chr1 | 56945077 | |||||||
| chr1:56945097 | C | A | 1 | a0001c0001t0002g0183 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1105+724G>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 7/11 | chr1 | 56945097 | |||||||
| chr1:56945105 | T | C | 4 | a0001c0001t0001g0174 a0001c0001t0001g0215 a0001c0001t0001g0274 others(1): Show |
4 | NA18940.hp1 NA19060.hp2 NA19083.hp1 others(1): Show |
intron_variant | MODIFIER | c.1105+716A>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 7/11 | chr1 | 56945105 | |||||||
| chr1:56945229 | C | A | 48 | a0001c0001t0001g0003 a0001c0001t0001g0030 a0001c0001t0001g0031 others(45): Show |
62 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(59): Show |
intron_variant | MODIFIER | c.1105+592G>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 7/11 | chr1 | 56945229 | |||||||
| chr1:56945452 | C | T | 1 | a0001c0001t0001g0206 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1105+369G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 7/11 | chr1 | 56945452 | |||||||
| chr1:56945527 | GCAGGAAG others(16): Show |
G | 2 | a0001c0001t0002g0090 a0001c0001t0002g0091 |
2 | HG01884.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1105+271_1105+293d others(25): Show |
C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 7/11 | chr1 | 56945527 | |||||||
| chr1:56945742 | G | T | 1 | a0001c0001t0001g0156 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1105+79C>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 7/11 | chr1 | 56945742 | |||||||
| chr1:56946106 | G | A | 3 | a0001c0001t0001g0164 a0001c0001t0002g0037 a0001c0001t0002g0165 |
4 | HG01515.hp1 HG01928.hp2 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.865-45C>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 6/11 | chr1 | 56946106 | |||||||
| chr1:56946456 | G | A | 1 | a0002c0002t0001g0224 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.865-395C>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 6/11 | chr1 | 56946456 | |||||||
| chr1:56946523 | A | G | 1 | a0001c0001t0001g0175 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.865-462T>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 6/11 | chr1 | 56946523 | |||||||
| chr1:56946587 | C | T | 66 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(63): Show |
111 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(108): Show |
intron_variant | MODIFIER | c.865-526G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 6/11 | chr1 | 56946587 | |||||||
| chr1:56946795 | T | C | 3 | a0001c0001t0001g0253 a0001c0001t0002g0005 a0001c0001t0002g0281 |
8 | HG01081.hp1 HG01884.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.865-734A>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 6/11 | chr1 | 56946795 | |||||||
| chr1:56946816 | A | G | 1 | a0001c0001t0001g0185 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.865-755T>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 6/11 | chr1 | 56946816 | |||||||
| chr1:56947069 | T | C | 13 | a0001c0001t0001g0025 a0001c0001t0001g0062 a0001c0001t0001g0063 others(10): Show |
15 | HG01255.hp1 HG02055.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.865-1008A>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 6/11 | chr1 | 56947069 | |||||||
| chr1:56947175 | G | T | 104 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0016 others(101): Show |
144 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(141): Show |
intron_variant | MODIFIER | c.865-1114C>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 6/11 | chr1 | 56947175 | |||||||
| chr1:56947274 | T | C | 47 | a0001c0001t0001g0003 a0001c0001t0001g0030 a0001c0001t0001g0031 others(44): Show |
61 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(58): Show |
intron_variant | MODIFIER | c.865-1213A>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 6/11 | chr1 | 56947274 | |||||||
| chr1:56947298 | T | C | 1 | a0001c0001t0001g0150 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.865-1237A>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 6/11 | chr1 | 56947298 | |||||||
| chr1:56947522 | C | G | 1 | a0001c0001t0001g0206 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.865-1461G>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 6/11 | chr1 | 56947522 | |||||||
| chr1:56947660 | G | A | 1 | a0001c0001t0001g0207 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.865-1599C>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 6/11 | chr1 | 56947660 | |||||||
| chr1:56947775 | C | CA | 25 | a0001c0001t0001g0014 a0001c0001t0001g0061 a0001c0001t0001g0069 others(22): Show |
30 | HG00597.hp1 HG00639.hp2 HG01256.hp1 others(27): Show |
intron_variant | MODIFIER | c.865-1715dupT | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 6/11 | chr1 | 56947775 | |||||||
| chr1:56947869 | T | C | 1 | a0001c0001t0002g0060 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.864+1686A>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 6/11 | chr1 | 56947869 | |||||||
| chr1:56947919 | A | G | 13 | a0001c0001t0001g0025 a0001c0001t0001g0062 a0001c0001t0001g0063 others(10): Show |
15 | HG01255.hp1 HG02055.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.864+1636T>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 6/11 | chr1 | 56947919 | |||||||
| chr1:56947951 | CA | C | 48 | a0001c0001t0001g0003 a0001c0001t0001g0030 a0001c0001t0001g0031 others(45): Show |
62 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(59): Show |
intron_variant | MODIFIER | c.864+1603delT | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 6/11 | chr1 | 56947951 | |||||||
| chr1:56947952 | A | AAAAC | 137 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0014 others(134): Show |
183 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(180): Show |
intron_variant | MODIFIER | c.864+1599_864+1602d others(6): Show |
C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 6/11 | chr1 | 56947952 | |||||||
| chr1:56948039 | A | T | 2 | a0001c0001t0001g0052 a0001c0001t0001g0242 |
3 | HG01175.hp2 HG03098.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.864+1516T>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 6/11 | chr1 | 56948039 | |||||||
| chr1:56948095 | G | A | 185 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0013 others(182): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.864+1460C>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 6/11 | chr1 | 56948095 | |||||||
| chr1:56948175 | G | A | 1 | a0001c0001t0001g0177 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.864+1380C>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 6/11 | chr1 | 56948175 | |||||||
| chr1:56948258 | CTATT | C | 4 | a0001c0001t0001g0171 a0001c0001t0001g0204 a0001c0001t0001g0250 others(1): Show |
4 | HG02258.hp1 HG02559.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.864+1293_864+1296d others(6): Show |
C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 6/11 | chr1 | 56948258 | |||||||
| chr1:56948569 | T | C | 2 | a0001c0005t0001g0137 a0001c0005t0001g0138 |
2 | HG03654.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.864+986A>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 6/11 | chr1 | 56948569 | |||||||
| chr1:56948641 | G | A | 2 | a0001c0001t0002g0216 a0001c0001t0002g0217 |
2 | HG00140.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.864+914C>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 6/11 | chr1 | 56948641 | |||||||
| chr1:56948763 | A | G | 4 | a0001c0001t0001g0174 a0001c0001t0001g0215 a0001c0001t0001g0274 others(1): Show |
4 | NA18940.hp1 NA19060.hp2 NA19083.hp1 others(1): Show |
intron_variant | MODIFIER | c.864+792T>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 6/11 | chr1 | 56948763 | |||||||
| chr1:56948880 | A | G | 4 | a0001c0001t0001g0174 a0001c0001t0001g0215 a0001c0001t0001g0274 others(1): Show |
4 | NA18940.hp1 NA19060.hp2 NA19083.hp1 others(1): Show |
intron_variant | MODIFIER | c.864+675T>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 6/11 | chr1 | 56948880 | |||||||
| chr1:56949008 | A | AT | 87 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0016 others(84): Show |
125 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(122): Show |
intron_variant | MODIFIER | c.864+546dupA | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 6/11 | chr1 | 56949008 | |||||||
| chr1:56949008 | AT | A | 23 | a0001c0001t0001g0025 a0001c0001t0001g0062 a0001c0001t0001g0063 others(20): Show |
27 | HG00639.hp2 HG01070.hp1 HG01192.hp1 others(24): Show |
intron_variant | MODIFIER | c.864+546delA | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 6/11 | chr1 | 56949008 | |||||||
| chr1:56949073 | C | T | 1 | a0001c0001t0001g0272 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.864+482G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 6/11 | chr1 | 56949073 | |||||||
| chr1:56949152 | A | G | 1 | a0001c0001t0002g0209 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.864+403T>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 6/11 | chr1 | 56949152 | |||||||
| chr1:56949341 | T | G | 1 | a0001c0001t0002g0099 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.864+214A>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 6/11 | chr1 | 56949341 | |||||||
| chr1:56949527 | C | T | 25 | a0001c0001t0001g0014 a0001c0001t0001g0061 a0001c0001t0001g0069 others(22): Show |
30 | HG00597.hp1 HG00639.hp2 HG01256.hp1 others(27): Show |
intron_variant | MODIFIER | c.864+28G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 6/11 | chr1 | 56949527 | |||||||
| chr1:56949778 | T | C | 1 | a0001c0001t0001g0085 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.667-26A>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 5/11 | chr1 | 56949778 | |||||||
| chr1:56949920 | C | T | 2 | a0001c0001t0001g0193 a0001c0001t0001g0200 |
2 | NA18990.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.667-168G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 5/11 | chr1 | 56949920 | |||||||
| chr1:56949921 | A | G | 185 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0013 others(182): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.667-169T>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 5/11 | chr1 | 56949921 | |||||||
| chr1:56949922 | G | T | 24 | a0001c0001t0001g0014 a0001c0001t0001g0061 a0001c0001t0001g0069 others(21): Show |
29 | HG00597.hp1 HG00639.hp2 HG01256.hp1 others(26): Show |
intron_variant | MODIFIER | c.667-170C>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 5/11 | chr1 | 56949922 | |||||||
| chr1:56950050 | G | T | 65 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(62): Show |
110 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.667-298C>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 5/11 | chr1 | 56950050 | |||||||
| chr1:56950066 | G | A | 2 | a0001c0001t0001g0193 a0001c0001t0001g0200 |
2 | NA18990.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.667-314C>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 5/11 | chr1 | 56950066 | |||||||
| chr1:56950293 | A | G | 185 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0013 others(182): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.667-541T>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 5/11 | chr1 | 56950293 | |||||||
| chr1:56950472 | A | G | 2 | a0002c0002t0001g0050 a0002c0002t0001g0223 |
3 | HG01192.hp1 HG01891.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.667-720T>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 5/11 | chr1 | 56950472 | |||||||
| chr1:56950529 | G | T | 1 | a0001c0001t0001g0148 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.667-777C>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 5/11 | chr1 | 56950529 | |||||||
| chr1:56950579 | C | T | 1 | a0001c0001t0001g0220 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.667-827G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 5/11 | chr1 | 56950579 | |||||||
| chr1:56950652 | A | T | 1 | a0001c0001t0001g0278 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.667-900T>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 5/11 | chr1 | 56950652 | |||||||
| chr1:56950662 | G | A | 85 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0016 others(82): Show |
123 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(120): Show |
intron_variant | MODIFIER | c.667-910C>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 5/11 | chr1 | 56950662 | |||||||
| chr1:56950774 | C | T | 13 | a0001c0001t0001g0025 a0001c0001t0001g0062 a0001c0001t0001g0063 others(10): Show |
15 | HG01255.hp1 HG02055.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.667-1022G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 5/11 | chr1 | 56950774 | |||||||
| chr1:56950856 | G | A | 13 | a0001c0001t0001g0025 a0001c0001t0001g0062 a0001c0001t0001g0063 others(10): Show |
15 | HG01255.hp1 HG02055.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.667-1104C>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 5/11 | chr1 | 56950856 | |||||||
| chr1:56950927 | A | G | 104 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0016 others(101): Show |
144 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(141): Show |
intron_variant | MODIFIER | c.666+1121T>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 5/11 | chr1 | 56950927 | |||||||
| chr1:56950960 | C | A | 74 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0030 others(71): Show |
93 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.666+1088G>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 5/11 | chr1 | 56950960 | |||||||
| chr1:56950978 | A | C | 1 | a0001c0001t0001g0208 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.666+1070T>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 5/11 | chr1 | 56950978 | |||||||
| chr1:56951335 | A | C | 1 | a0001c0001t0001g0213 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.666+713T>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 5/11 | chr1 | 56951335 | |||||||
| chr1:56951411 | C | T | 1 | a0001c0001t0002g0147 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.666+637G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 5/11 | chr1 | 56951411 | |||||||
| chr1:56951419 | A | G | 2 | a0001c0001t0001g0144 a0001c0001t0001g0145 |
2 | HG02965.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.666+629T>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 5/11 | chr1 | 56951419 | |||||||
| chr1:56951435 | T | C | 185 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0013 others(182): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.666+613A>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 5/11 | chr1 | 56951435 | |||||||
| chr1:56951685 | G | A | 13 | a0001c0001t0001g0025 a0001c0001t0001g0062 a0001c0001t0001g0063 others(10): Show |
15 | HG01255.hp1 HG02055.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.666+363C>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 5/11 | chr1 | 56951685 | |||||||
| chr1:56951711 | T | C | 3 | a0001c0001t0001g0174 a0001c0001t0001g0215 a0001c0001t0001g0275 |
3 | NA18940.hp1 NA19060.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.666+337A>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 5/11 | chr1 | 56951711 | |||||||
| chr1:56951919 | C | A | 49 | a0001c0001t0001g0003 a0001c0001t0001g0030 a0001c0001t0001g0031 others(46): Show |
63 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(60): Show |
intron_variant | MODIFIER | c.666+129G>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 5/11 | chr1 | 56951919 | |||||||
| chr1:56951960 | G | GGGATGTG others(14): Show |
185 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0013 others(182): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.666+87_666+88insTG others(19): Show |
C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 5/11 | chr1 | 56951960 | |||||||
| chr1:56952219 | T | C | 1 | a0001c0001t0001g0213 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.534-39A>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 4/11 | chr1 | 56952219 | |||||||
| chr1:56952257 | C | T | 1 | a0001c0001t0001g0253 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.534-77G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 4/11 | chr1 | 56952257 | |||||||
| chr1:56952383 | G | C | 5 | a0001c0001t0001g0031 a0001c0001t0001g0109 a0001c0001t0001g0148 others(2): Show |
6 | HG00323.hp1 HG01168.hp2 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.534-203C>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 4/11 | chr1 | 56952383 | |||||||
| chr1:56952512 | T | C | 1 | a0001c0001t0001g0100 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.534-332A>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 4/11 | chr1 | 56952512 | |||||||
| chr1:56952593 | C | T | 1 | a0001c0001t0001g0178 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.534-413G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 4/11 | chr1 | 56952593 | |||||||
| chr1:56952687 | G | A | 1 | a0001c0001t0002g0172 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.534-507C>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 4/11 | chr1 | 56952687 | |||||||
| chr1:56952711 | C | T | 13 | a0001c0001t0001g0025 a0001c0001t0001g0062 a0001c0001t0001g0063 others(10): Show |
15 | HG01255.hp1 HG02055.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.534-531G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 4/11 | chr1 | 56952711 | |||||||
| chr1:56952740 | G | A | 49 | a0001c0001t0001g0003 a0001c0001t0001g0030 a0001c0001t0001g0031 others(46): Show |
63 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(60): Show |
intron_variant | MODIFIER | c.534-560C>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 4/11 | chr1 | 56952740 | |||||||
| chr1:56952876 | C | T | 3 | a0001c0001t0001g0152 a0001c0001t0001g0228 a0001c0004t0001g0229 |
3 | HG01109.hp2 HG01243.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.534-696G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 4/11 | chr1 | 56952876 | |||||||
| chr1:56952881 | T | A | 4 | a0001c0001t0001g0171 a0001c0001t0001g0204 a0001c0001t0001g0250 others(1): Show |
4 | HG02258.hp1 HG02559.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.534-701A>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 4/11 | chr1 | 56952881 | |||||||
| chr1:56952891 | T | A | 2 | a0001c0001t0001g0086 a0001c0001t0001g0181 |
2 | HG02559.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.534-711A>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 4/11 | chr1 | 56952891 | |||||||
| chr1:56952984 | G | A | 1 | a0001c0001t0001g0213 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.534-804C>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 4/11 | chr1 | 56952984 | |||||||
| chr1:56953053 | G | A | 2 | a0002c0002t0001g0283 a0002c0002t0002g0282 |
2 | HG01070.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.534-873C>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 4/11 | chr1 | 56953053 | |||||||
| chr1:56953096 | C | A | 4 | a0001c0001t0001g0171 a0001c0001t0001g0204 a0001c0001t0001g0250 others(1): Show |
4 | HG02258.hp1 HG02559.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.534-916G>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 4/11 | chr1 | 56953096 | |||||||
| chr1:56953103 | T | C | 1 | a0001c0001t0001g0201 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.534-923A>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 4/11 | chr1 | 56953103 | |||||||
| chr1:56953384 | G | A | 1 | a0001c0001t0001g0068 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.534-1204C>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 4/11 | chr1 | 56953384 | |||||||
| chr1:56953553 | C | A | 182 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0013 others(179): Show |
242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
intron_variant | MODIFIER | c.533+1133G>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 4/11 | chr1 | 56953553 | |||||||
| chr1:56953614 | G | A | 149 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0013 others(146): Show |
203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.533+1072C>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 4/11 | chr1 | 56953614 | |||||||
| chr1:56953709 | G | A | 1 | a0001c0001t0001g0108 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.533+977C>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 4/11 | chr1 | 56953709 | |||||||
| chr1:56953858 | G | A | 11 | a0001c0001t0001g0025 a0001c0001t0001g0062 a0001c0001t0001g0063 others(8): Show |
12 | HG01255.hp1 HG02055.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.533+828C>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 4/11 | chr1 | 56953858 | |||||||
| chr1:56953884 | T | C | 1 | a0001c0001t0001g0103 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.533+802A>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 4/11 | chr1 | 56953884 | |||||||
| chr1:56953934 | T | C | 186 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0013 others(183): Show |
246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.533+752A>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 4/11 | chr1 | 56953934 | |||||||
| chr1:56953997 | T | A | 1 | a0001c0001t0001g0174 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.533+689A>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 4/11 | chr1 | 56953997 | |||||||
| chr1:56954131 | G | T | 2 | a0001c0001t0001g0052 a0001c0001t0001g0242 |
3 | HG01175.hp2 HG03098.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.533+555C>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 4/11 | chr1 | 56954131 | |||||||
| chr1:56954209 | A | G | 13 | a0001c0001t0001g0025 a0001c0001t0001g0062 a0001c0001t0001g0063 others(10): Show |
15 | HG01255.hp1 HG02055.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.533+477T>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 4/11 | chr1 | 56954209 | |||||||
| chr1:56954274 | C | T | 2 | a0001c0001t0001g0052 a0001c0001t0001g0242 |
3 | HG01175.hp2 HG03098.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.533+412G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 4/11 | chr1 | 56954274 | |||||||
| chr1:56954334 | A | C | 1 | a0001c0001t0001g0113 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.533+352T>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 4/11 | chr1 | 56954334 | |||||||
| chr1:56954370 | T | C | 149 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0013 others(146): Show |
203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.533+316A>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 4/11 | chr1 | 56954370 | |||||||
| chr1:56954403 | C | A | 2 | a0001c0001t0001g0052 a0001c0001t0001g0242 |
3 | HG01175.hp2 HG03098.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.533+283G>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 4/11 | chr1 | 56954403 | |||||||
| chr1:56954429 | G | A | 2 | a0001c0001t0001g0222 a0001c0001t0001g0243 |
2 | HG02572.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.533+257C>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 4/11 | chr1 | 56954429 | |||||||
| chr1:56954486 | A | G | 1 | a0001c0001t0002g0252 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.533+200T>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 4/11 | chr1 | 56954486 | |||||||
| chr1:56954513 | A | G | 1 | a0001c0001t0001g0109 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.533+173T>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 4/11 | chr1 | 56954513 | |||||||
| chr1:56954625 | C | A | 2 | a0001c0005t0001g0137 a0001c0005t0001g0138 |
2 | HG03654.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.533+61G>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 4/11 | chr1 | 56954625 | |||||||
| chr1:56954625 | C | T | 2 | a0001c0001t0002g0087 a0001c0001t0002g0112 |
2 | HG04115.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.533+61G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 4/11 | chr1 | 56954625 | |||||||
| chr1:56954663 | G | A | 3 | a0001c0001t0001g0269 a0001c0005t0001g0137 a0001c0005t0001g0138 |
3 | HG02083.hp2 HG03654.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.533+23C>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 4/11 | chr1 | 56954663 | |||||||
| chr1:56954856 | G | A | 2 | a0001c0001t0002g0251 a0001c0001t0002g0270 |
2 | NA18979.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.392-29C>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 3/11 | chr1 | 56954856 | |||||||
| chr1:56954954 | A | G | 7 | a0002c0002t0001g0050 a0002c0002t0001g0176 a0002c0002t0001g0223 others(4): Show |
8 | HG01070.hp1 HG01192.hp1 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.392-127T>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 3/11 | chr1 | 56954954 | |||||||
| chr1:56955094 | G | A | 1 | a0001c0001t0001g0103 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.392-267C>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 3/11 | chr1 | 56955094 | |||||||
| chr1:56955220 | G | A | 1 | a0001c0001t0001g0271 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.392-393C>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 3/11 | chr1 | 56955220 | |||||||
| chr1:56955265 | C | G | 2 | a0001c0001t0001g0023 a0001c0001t0001g0170 |
4 | NA18943.hp1 NA18992.hp2 NA19068.hp1 others(1): Show |
intron_variant | MODIFIER | c.392-438G>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 3/11 | chr1 | 56955265 | |||||||
| chr1:56955284 | A | G | 149 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0013 others(146): Show |
203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.392-457T>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 3/11 | chr1 | 56955284 | |||||||
| chr1:56955414 | A | T | 1 | a0001c0001t0001g0103 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.392-587T>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 3/11 | chr1 | 56955414 | |||||||
| chr1:56955436 | C | T | 4 | a0001c0001t0001g0171 a0001c0001t0001g0204 a0001c0001t0001g0250 others(1): Show |
4 | HG02258.hp1 HG02559.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.392-609G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 3/11 | chr1 | 56955436 | |||||||
| chr1:56955493 | C | T | 149 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0013 others(146): Show |
203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.392-666G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 3/11 | chr1 | 56955493 | |||||||
| chr1:56955648 | A | T | 1 | a0001c0001t0001g0026 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.392-821T>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 3/11 | chr1 | 56955648 | |||||||
| chr1:56955664 | A | G | 186 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0013 others(183): Show |
246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.392-837T>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 3/11 | chr1 | 56955664 | |||||||
| chr1:56955718 | C | T | 1 | a0001c0001t0002g0076 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.392-891G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 3/11 | chr1 | 56955718 | |||||||
| chr1:56955838 | A | G | 11 | a0001c0001t0001g0025 a0001c0001t0001g0062 a0001c0001t0001g0063 others(8): Show |
12 | HG01255.hp1 HG02055.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.391+931T>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 3/11 | chr1 | 56955838 | |||||||
| chr1:56956083 | C | T | 1 | a0001c0001t0001g0069 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.391+686G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 3/11 | chr1 | 56956083 | |||||||
| chr1:56956102 | A | G | 179 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0013 others(176): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.391+667T>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 3/11 | chr1 | 56956102 | |||||||
| chr1:56956102 | A | T | 7 | a0002c0002t0001g0050 a0002c0002t0001g0176 a0002c0002t0001g0223 others(4): Show |
8 | HG01070.hp1 HG01192.hp1 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.391+667T>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 3/11 | chr1 | 56956102 | |||||||
| chr1:56956111 | T | C | 1 | a0001c0001t0001g0199 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.391+658A>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 3/11 | chr1 | 56956111 | |||||||
| chr1:56956314 | C | T | 186 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0013 others(183): Show |
246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.391+455G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 3/11 | chr1 | 56956314 | |||||||
| chr1:56956318 | A | C | 49 | a0001c0001t0001g0003 a0001c0001t0001g0030 a0001c0001t0001g0031 others(46): Show |
63 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(60): Show |
intron_variant | MODIFIER | c.391+451T>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 3/11 | chr1 | 56956318 | |||||||
| chr1:56956405 | A | G | 1 | a0001c0001t0001g0248 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.391+364T>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 3/11 | chr1 | 56956405 | |||||||
| chr1:56956448 | G | A | 4 | a0001c0001t0001g0171 a0001c0001t0001g0204 a0001c0001t0001g0250 others(1): Show |
4 | HG02258.hp1 HG02559.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.391+321C>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 3/11 | chr1 | 56956448 | |||||||
| chr1:56956543 | C | T | 1 | a0001c0001t0001g0150 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.391+226G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 3/11 | chr1 | 56956543 | |||||||
| chr1:56956545 | T | C | 186 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0013 others(183): Show |
246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.391+224A>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 3/11 | chr1 | 56956545 | |||||||
| chr1:56956745 | T | C | 2 | a0001c0001t0001g0065 a0001c0001t0001g0066 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.391+24A>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 3/11 | chr1 | 56956745 | |||||||
| chr1:56956930 | G | C | 13 | a0001c0001t0001g0025 a0001c0001t0001g0062 a0001c0001t0001g0063 others(10): Show |
15 | HG01255.hp1 HG02055.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.250-20C>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 2/11 | chr1 | 56956930 | |||||||
| chr1:56956966 | G | A | 1 | a0001c0001t0001g0272 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.250-56C>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 2/11 | chr1 | 56956966 | |||||||
| chr1:56957123 | A | G | 1 | a0001c0001t0001g0276 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.250-213T>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 2/11 | chr1 | 56957123 | |||||||
| chr1:56957258 | T | C | 85 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0016 others(82): Show |
123 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(120): Show |
intron_variant | MODIFIER | c.250-348A>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 2/11 | chr1 | 56957258 | |||||||
| chr1:56957271 | CCAGTTCA others(30): Show |
C | 1 | a0001c0001t0001g0279 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.250-398_250-362del others(37): Show |
C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 2/11 | chr1 | 56957271 | |||||||
| chr1:56957834 | C | T | 257 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(254): Show |
363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
intron_variant | MODIFIER | c.250-924G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 2/11 | chr1 | 56957834 | |||||||
| chr1:56957940 | TCTGACAG others(10): Show |
T | 1 | a0001c0001t0001g0149 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.250-1047_250-1031d others(19): Show |
C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 2/11 | chr1 | 56957940 | |||||||
| chr1:56957962 | C | G | 182 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0013 others(179): Show |
242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
intron_variant | MODIFIER | c.250-1052G>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 2/11 | chr1 | 56957962 | |||||||
| chr1:56957992 | T | G | 1 | a0001c0004t0001g0153 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.250-1082A>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 2/11 | chr1 | 56957992 | |||||||
| chr1:56958068 | T | C | 4 | a0001c0001t0001g0171 a0001c0001t0001g0204 a0001c0001t0001g0250 others(1): Show |
4 | HG02258.hp1 HG02559.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.250-1158A>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 2/11 | chr1 | 56958068 | |||||||
| chr1:56958110 | T | A | 49 | a0001c0001t0001g0003 a0001c0001t0001g0030 a0001c0001t0001g0031 others(46): Show |
63 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(60): Show |
intron_variant | MODIFIER | c.250-1200A>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 2/11 | chr1 | 56958110 | |||||||
| chr1:56958495 | G | GA | 5 | a0001c0001t0001g0023 a0001c0001t0001g0156 a0001c0001t0001g0157 others(2): Show |
7 | HG01891.hp2 HG02965.hp2 NA18943.hp1 others(4): Show |
intron_variant | MODIFIER | c.249+1524dupT | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 2/11 | chr1 | 56958495 | |||||||
| chr1:56958510 | A | G | 4 | a0001c0001t0001g0171 a0001c0001t0001g0204 a0001c0001t0001g0250 others(1): Show |
4 | HG02258.hp1 HG02559.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.249+1510T>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 2/11 | chr1 | 56958510 | |||||||
| chr1:56958551 | G | T | 4 | a0001c0001t0001g0171 a0001c0001t0001g0204 a0001c0001t0001g0250 others(1): Show |
4 | HG02258.hp1 HG02559.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.249+1469C>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 2/11 | chr1 | 56958551 | |||||||
| chr1:56958595 | GC | G | 12 | a0001c0001t0001g0025 a0001c0001t0001g0062 a0001c0001t0001g0063 others(9): Show |
14 | HG01255.hp1 HG02055.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.249+1424delG | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 2/11 | chr1 | 56958595 | |||||||
| chr1:56958597 | T | A | 12 | a0001c0001t0001g0025 a0001c0001t0001g0062 a0001c0001t0001g0063 others(9): Show |
14 | HG01255.hp1 HG02055.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.249+1423A>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 2/11 | chr1 | 56958597 | |||||||
| chr1:56958623 | T | G | 3 | a0001c0001t0001g0068 a0001c0004t0001g0024 a0007c0011t0001g0067 |
4 | HG02055.hp1 HG02486.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.249+1397A>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 2/11 | chr1 | 56958623 | |||||||
| chr1:56959046 | A | G | 25 | a0001c0001t0001g0014 a0001c0001t0001g0061 a0001c0001t0001g0069 others(22): Show |
30 | HG00597.hp1 HG01256.hp1 HG01258.hp2 others(27): Show |
intron_variant | MODIFIER | c.249+974T>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 2/11 | chr1 | 56959046 | |||||||
| chr1:56959062 | T | C | 257 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(254): Show |
363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
intron_variant | MODIFIER | c.249+958A>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 2/11 | chr1 | 56959062 | |||||||
| chr1:56959145 | T | C | 1 | a0001c0001t0002g0135 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.249+875A>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 2/11 | chr1 | 56959145 | |||||||
| chr1:56959365 | G | A | 3 | a0001c0001t0001g0166 a0001c0001t0001g0207 a0001c0001t0002g0038 |
4 | NA18950.hp1 NA18966.hp1 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.249+655C>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 2/11 | chr1 | 56959365 | |||||||
| chr1:56959471 | G | A | 4 | a0001c0001t0001g0171 a0001c0001t0001g0204 a0001c0001t0001g0250 others(1): Show |
4 | HG02258.hp1 HG02559.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.249+549C>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 2/11 | chr1 | 56959471 | |||||||
| chr1:56959552 | G | A | 1 | a0001c0001t0001g0175 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.249+468C>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 2/11 | chr1 | 56959552 | |||||||
| chr1:56959567 | A | G | 1 | a0001c0001t0002g0251 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.249+453T>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 2/11 | chr1 | 56959567 | |||||||
| chr1:56959587 | T | G | 1 | a0001c0001t0002g0196 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.249+433A>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 2/11 | chr1 | 56959587 | |||||||
| chr1:56959616 | C | T | 1 | a0001c0001t0001g0149 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.249+404G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 2/11 | chr1 | 56959616 | |||||||
| chr1:56959648 | G | A | 12 | a0001c0001t0001g0025 a0001c0001t0001g0062 a0001c0001t0001g0063 others(9): Show |
14 | HG01255.hp1 HG02055.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.249+372C>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 2/11 | chr1 | 56959648 | |||||||
| chr1:56959745 | T | C | 6 | a0001c0001t0001g0174 a0001c0001t0001g0215 a0001c0001t0001g0274 others(3): Show |
7 | HG02738.hp1 HG03491.hp2 HG03688.hp2 others(4): Show |
intron_variant | MODIFIER | c.249+275A>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 2/11 | chr1 | 56959745 | |||||||
| chr1:56959801 | A | T | 84 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0016 others(81): Show |
121 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(118): Show |
intron_variant | MODIFIER | c.249+219T>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 2/11 | chr1 | 56959801 | |||||||
| chr1:56959881 | G | A | 1 | a0001c0001t0001g0045 | 2 | HG03139.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.249+139C>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 2/11 | chr1 | 56959881 | |||||||
| chr1:56960206 | C | T | 16 | a0001c0001t0001g0025 a0001c0001t0001g0062 a0001c0001t0001g0063 others(13): Show |
18 | HG01255.hp1 HG02055.hp1 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.93-30G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56960206 | |||||||
| chr1:56960215 | AG | A | 30 | a0001c0001t0001g0003 a0001c0001t0001g0031 a0001c0001t0001g0044 others(27): Show |
41 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(38): Show |
intron_variant | MODIFIER | c.93-40delC | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56960215 | |||||||
| chr1:56960225 | G | A | 1 | a0001c0001t0001g0083 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.93-49C>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56960225 | |||||||
| chr1:56960344 | T | TA | 3 | a0001c0001t0001g0052 a0001c0001t0001g0242 a0001c0001t0001g0243 |
4 | HG01175.hp2 HG03098.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.93-169dupT | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56960344 | |||||||
| chr1:56960409 | T | C | 1 | a0007c0011t0001g0067 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.93-233A>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56960409 | |||||||
| chr1:56960434 | A | T | 1 | a0001c0001t0001g0022 | 3 | HG02056.hp1 NA18612.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.93-258T>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56960434 | |||||||
| chr1:56960471 | A | G | 19 | a0001c0001t0001g0025 a0001c0001t0001g0062 a0001c0001t0001g0063 others(16): Show |
21 | HG01255.hp1 HG02055.hp1 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.93-295T>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56960471 | |||||||
| chr1:56960492 | C | T | 2 | a0001c0005t0001g0137 a0001c0005t0001g0138 |
2 | HG03654.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.93-316G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56960492 | |||||||
| chr1:56960585 | G | C | 1 | a0001c0001t0001g0206 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.93-409C>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56960585 | |||||||
| chr1:56960624 | G | C | 1 | a0001c0001t0002g0135 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.93-448C>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56960624 | |||||||
| chr1:56960720 | A | T | 1 | a0001c0004t0001g0153 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.93-544T>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56960720 | |||||||
| chr1:56960781 | T | C | 82 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0016 others(79): Show |
119 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(116): Show |
intron_variant | MODIFIER | c.93-605A>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56960781 | |||||||
| chr1:56960849 | G | C | 2 | a0001c0005t0001g0137 a0001c0005t0001g0138 |
2 | HG03654.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.93-673C>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56960849 | |||||||
| chr1:56960856 | G | A | 2 | a0001c0005t0001g0137 a0001c0005t0001g0138 |
2 | HG03654.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.93-680C>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56960856 | |||||||
| chr1:56960897 | G | A | 3 | a0001c0001t0001g0057 a0001c0001t0001g0276 a0001c0001t0001g0277 |
4 | HG02257.hp2 HG02280.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.93-721C>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56960897 | |||||||
| chr1:56961029 | G | T | 1 | a0001c0001t0001g0213 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.93-853C>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56961029 | |||||||
| chr1:56961120 | G | A | 1 | a0001c0001t0002g0075 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.93-944C>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56961120 | |||||||
| chr1:56961208 | A | T | 2 | a0001c0005t0001g0137 a0001c0005t0001g0138 |
2 | HG03654.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.93-1032T>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56961208 | |||||||
| chr1:56961224 | T | G | 6 | a0001c0001t0001g0171 a0001c0001t0001g0204 a0001c0001t0001g0250 others(3): Show |
6 | HG02258.hp1 HG02559.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.93-1048A>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56961224 | |||||||
| chr1:56961277 | T | C | 7 | a0002c0002t0001g0050 a0002c0002t0001g0176 a0002c0002t0001g0223 others(4): Show |
8 | HG01070.hp1 HG01192.hp1 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.93-1101A>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56961277 | |||||||
| chr1:56961298 | G | A | 2 | a0001c0005t0001g0137 a0001c0005t0001g0138 |
2 | HG03654.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.93-1122C>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56961298 | |||||||
| chr1:56961412 | C | A | 1 | a0001c0001t0001g0131 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.93-1236G>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56961412 | |||||||
| chr1:56961438 | C | T | 8 | a0001c0001t0001g0014 a0001c0001t0001g0061 a0001c0001t0001g0093 others(5): Show |
11 | HG02615.hp1 HG02630.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.93-1262G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56961438 | |||||||
| chr1:56961450 | G | T | 19 | a0001c0001t0001g0025 a0001c0001t0001g0062 a0001c0001t0001g0063 others(16): Show |
21 | HG01255.hp1 HG02055.hp1 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.93-1274C>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56961450 | |||||||
| chr1:56961462 | G | T | 19 | a0001c0001t0001g0025 a0001c0001t0001g0062 a0001c0001t0001g0063 others(16): Show |
21 | HG01255.hp1 HG02055.hp1 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.93-1286C>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56961462 | |||||||
| chr1:56961547 | C | T | 2 | a0001c0001t0001g0032 a0001c0001t0001g0089 |
3 | NA18946.hp2 NA18955.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.93-1371G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56961547 | |||||||
| chr1:56961573 | C | T | 1 | a0001c0001t0001g0111 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.93-1397G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56961573 | |||||||
| chr1:56961578 | C | A | 29 | a0001c0001t0001g0014 a0001c0001t0001g0061 a0001c0001t0001g0069 others(26): Show |
34 | HG00597.hp1 HG00639.hp2 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.93-1402G>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56961578 | |||||||
| chr1:56961591 | T | G | 1 | a0001c0001t0001g0148 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.93-1415A>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56961591 | |||||||
| chr1:56961628 | T | C | 3 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0132 |
5 | HG02451.hp1 HG02622.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.93-1452A>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56961628 | |||||||
| chr1:56961663 | C | T | 1 | a0001c0001t0001g0109 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.93-1487G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56961663 | |||||||
| chr1:56961768 | G | A | 13 | a0001c0001t0001g0025 a0001c0001t0001g0062 a0001c0001t0001g0063 others(10): Show |
15 | HG01255.hp1 HG02055.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.93-1592C>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56961768 | |||||||
| chr1:56961788 | C | A | 1 | a0001c0001t0001g0175 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.93-1612G>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56961788 | |||||||
| chr1:56961793 | A | C | 19 | a0001c0001t0001g0025 a0001c0001t0001g0062 a0001c0001t0001g0063 others(16): Show |
21 | HG01255.hp1 HG02055.hp1 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.93-1617T>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56961793 | |||||||
| chr1:56961830 | G | A | 50 | a0001c0001t0001g0003 a0001c0001t0001g0030 a0001c0001t0001g0031 others(47): Show |
64 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(61): Show |
intron_variant | MODIFIER | c.93-1654C>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56961830 | |||||||
| chr1:56961885 | G | A | 13 | a0001c0001t0001g0025 a0001c0001t0001g0062 a0001c0001t0001g0063 others(10): Show |
15 | HG01255.hp1 HG02055.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.93-1709C>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56961885 | |||||||
| chr1:56961971 | T | C | 12 | a0001c0001t0001g0025 a0001c0001t0001g0062 a0001c0001t0001g0063 others(9): Show |
14 | HG01255.hp1 HG02055.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.93-1795A>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56961971 | |||||||
| chr1:56962060 | A | G | 1 | a0001c0001t0001g0219 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.93-1884T>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56962060 | |||||||
| chr1:56962174 | T | G | 1 | a0001c0001t0001g0206 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.93-1998A>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56962174 | |||||||
| chr1:56962186 | A | G | 10 | a0001c0001t0001g0025 a0001c0001t0001g0062 a0001c0001t0001g0063 others(7): Show |
12 | HG01255.hp1 HG02055.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.93-2010T>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56962186 | |||||||
| chr1:56962187 | G | T | 4 | a0001c0001t0002g0072 a0001c0001t0002g0073 a0001c0001t0002g0074 others(1): Show |
4 | HG02027.hp2 NA18939.hp1 NA18988.hp2 others(1): Show |
intron_variant | MODIFIER | c.93-2011C>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56962187 | |||||||
| chr1:56962496 | C | A | 1 | a0001c0001t0001g0068 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.93-2320G>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56962496 | |||||||
| chr1:56962708 | A | G | 91 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0016 others(88): Show |
129 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(126): Show |
intron_variant | MODIFIER | c.93-2532T>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56962708 | |||||||
| chr1:56962730 | G | A | 2 | a0001c0005t0001g0137 a0001c0005t0001g0138 |
2 | HG03654.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.93-2554C>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56962730 | |||||||
| chr1:56962759 | G | A | 2 | a0001c0001t0001g0085 a0001c0001t0002g0147 |
2 | HG00639.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.93-2583C>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56962759 | |||||||
| chr1:56962916 | T | C | 84 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0016 others(81): Show |
119 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(116): Show |
intron_variant | MODIFIER | c.93-2740A>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56962916 | |||||||
| chr1:56963007 | T | C | 111 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(108): Show |
166 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(163): Show |
intron_variant | MODIFIER | c.93-2831A>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56963007 | |||||||
| chr1:56963047 | T | C | 2 | a0001c0001t0001g0198 a0001c0001t0001g0199 |
2 | HG03130.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.92+2810A>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56963047 | |||||||
| chr1:56963193 | C | T | 86 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0016 others(83): Show |
122 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(119): Show |
intron_variant | MODIFIER | c.92+2664G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56963193 | |||||||
| chr1:56963214 | G | A | 53 | a0001c0001t0001g0003 a0001c0001t0001g0030 a0001c0001t0001g0031 others(50): Show |
68 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(65): Show |
intron_variant | MODIFIER | c.92+2643C>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56963214 | |||||||
| chr1:56963221 | A | T | 1 | a0001c0001t0001g0068 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.92+2636T>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56963221 | |||||||
| chr1:56963299 | G | C | 1 | a0001c0001t0001g0069 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.92+2558C>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56963299 | |||||||
| chr1:56963449 | A | G | 1 | a0001c0001t0002g0246 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.92+2408T>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56963449 | |||||||
| chr1:56963466 | C | G | 1 | a0001c0001t0001g0245 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.92+2391G>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56963466 | |||||||
| chr1:56963466 | C | T | 1 | a0001c0001t0002g0049 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.92+2391G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56963466 | |||||||
| chr1:56963467 | G | A | 54 | a0001c0001t0001g0003 a0001c0001t0001g0030 a0001c0001t0001g0031 others(51): Show |
69 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(66): Show |
intron_variant | MODIFIER | c.92+2390C>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56963467 | |||||||
| chr1:56963499 | C | T | 53 | a0001c0001t0001g0003 a0001c0001t0001g0030 a0001c0001t0001g0031 others(50): Show |
68 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(65): Show |
intron_variant | MODIFIER | c.92+2358G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56963499 | |||||||
| chr1:56963531 | T | C | 33 | a0001c0001t0001g0003 a0001c0001t0001g0031 a0001c0001t0001g0044 others(30): Show |
44 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(41): Show |
intron_variant | MODIFIER | c.92+2326A>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56963531 | |||||||
| chr1:56963562 | A | G | 1 | a0001c0001t0001g0226 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.92+2295T>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56963562 | |||||||
| chr1:56963575 | A | G | 240 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(237): Show |
345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.92+2282T>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56963575 | |||||||
| chr1:56963589 | TG | T | 85 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(82): Show |
138 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.92+2267delC | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56963589 | |||||||
| chr1:56963590 | G | GGGGGTCA others(29): Show |
1 | a0001c0001t0001g0279 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.92+2266_92+2267ins others(36): Show |
C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56963590 | |||||||
| chr1:56963596 | T | C | 134 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0013 others(131): Show |
182 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(179): Show |
intron_variant | MODIFIER | c.92+2261A>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56963596 | |||||||
| chr1:56963597 | G | A | 78 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0016 others(75): Show |
111 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.92+2260C>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56963597 | |||||||
| chr1:56963651 | A | G | 138 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0013 others(135): Show |
187 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(184): Show |
intron_variant | MODIFIER | c.92+2206T>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56963651 | |||||||
| chr1:56963780 | G | C | 1 | a0001c0001t0001g0219 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.92+2077C>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56963780 | |||||||
| chr1:56963817 | C | T | 1 | a0001c0001t0001g0101 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.92+2040G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56963817 | |||||||
| chr1:56964274 | A | T | 5 | a0001c0001t0001g0052 a0001c0001t0001g0241 a0001c0001t0001g0242 others(2): Show |
6 | HG01175.hp2 HG01255.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.92+1583T>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56964274 | |||||||
| chr1:56964280 | T | C | 1 | a0001c0001t0001g0013 | 4 | NA18942.hp1 NA18951.hp2 NA18956.hp1 others(1): Show |
intron_variant | MODIFIER | c.92+1577A>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56964280 | |||||||
| chr1:56964286 | C | T | 6 | a0001c0001t0001g0014 a0001c0001t0001g0093 a0001c0001t0001g0144 others(3): Show |
9 | HG02615.hp1 HG02630.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.92+1571G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56964286 | |||||||
| chr1:56964365 | C | T | 1 | a0001c0001t0001g0171 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.92+1492G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56964365 | |||||||
| chr1:56964495 | C | T | 1 | a0001c0001t0001g0206 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.92+1362G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56964495 | |||||||
| chr1:56964554 | G | A | 11 | a0001c0001t0001g0025 a0001c0001t0001g0061 a0001c0001t0001g0062 others(8): Show |
13 | HG02055.hp1 HG02145.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.92+1303C>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56964554 | |||||||
| chr1:56964567 | G | A | 7 | a0001c0001t0001g0025 a0001c0001t0001g0062 a0001c0001t0001g0063 others(4): Show |
8 | HG02145.hp2 HG02647.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.92+1290C>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56964567 | |||||||
| chr1:56964629 | T | C | 1 | a0001c0001t0001g0070 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.92+1228A>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56964629 | |||||||
| chr1:56964668 | C | CT | 12 | a0001c0001t0001g0025 a0001c0001t0001g0061 a0001c0001t0001g0062 others(9): Show |
14 | HG02055.hp1 HG02145.hp2 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.92+1188_92+1189ins others(1): Show |
C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56964668 | |||||||
| chr1:56964668 | C | T | 1 | a0001c0001t0002g0240 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.92+1189G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56964668 | |||||||
| chr1:56964727 | G | A | 1 | a0007c0011t0001g0067 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.92+1130C>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56964727 | |||||||
| chr1:56964869 | C | T | 1 | a0001c0001t0001g0219 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.92+988G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56964869 | |||||||
| chr1:56964885 | G | C | 1 | a0001c0001t0001g0213 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.92+972C>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56964885 | |||||||
| chr1:56964910 | C | T | 2 | a0001c0001t0001g0018 a0001c0001t0001g0218 |
4 | HG01069.hp2 HG01071.hp1 HG01257.hp2 others(1): Show |
intron_variant | MODIFIER | c.92+947G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56964910 | |||||||
| chr1:56964973 | T | C | 1 | a0001c0001t0001g0069 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.92+884A>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56964973 | |||||||
| chr1:56965132 | C | A | 75 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(72): Show |
121 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.92+725G>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56965132 | |||||||
| chr1:56965162 | C | G | 1 | a0001c0001t0001g0206 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.92+695G>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56965162 | |||||||
| chr1:56965175 | A | T | 1 | a0001c0001t0001g0206 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.92+682T>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56965175 | |||||||
| chr1:56965213 | C | T | 90 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(87): Show |
139 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.92+644G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56965213 | |||||||
| chr1:56965222 | C | T | 1 | a0001c0001t0001g0069 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.92+635G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56965222 | |||||||
| chr1:56965311 | G | A | 27 | a0001c0001t0001g0025 a0001c0001t0001g0061 a0001c0001t0001g0062 others(24): Show |
30 | HG00597.hp1 HG00735.hp1 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.92+546C>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56965311 | |||||||
| chr1:56965332 | T | C | 1 | a0001c0001t0002g0239 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.92+525A>G | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56965332 | |||||||
| chr1:56965378 | T | TGAGA | 56 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(53): Show |
95 | HG00280.hp2 HG00408.hp2 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.92+475_92+478dupTC others(2): Show |
C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56965378 | |||||||
| chr1:56965392 | A | T | 9 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0095 others(6): Show |
14 | HG01069.hp1 HG01978.hp2 HG02004.hp2 others(11): Show |
intron_variant | MODIFIER | c.92+465T>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56965392 | |||||||
| chr1:56965394 | A | T | 9 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0095 others(6): Show |
14 | HG01069.hp1 HG01978.hp2 HG02004.hp2 others(11): Show |
intron_variant | MODIFIER | c.92+463T>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56965394 | |||||||
| chr1:56965396 | A | AGT | 7 | a0001c0001t0001g0152 a0001c0001t0002g0058 a0001c0001t0002g0059 others(4): Show |
9 | HG01070.hp1 HG01109.hp2 HG01256.hp1 others(6): Show |
intron_variant | MODIFIER | c.92+460_92+461insAC | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56965396 | |||||||
| chr1:56965396 | A | AGTGTGTG others(1): Show |
2 | a0001c0001t0001g0026 a0001c0001t0002g0087 |
3 | HG02896.hp1 HG02897.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.92+460_92+461insAC others(6): Show |
C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56965396 | |||||||
| chr1:56965396 | A | T | 9 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0095 others(6): Show |
14 | HG01069.hp1 HG01978.hp2 HG02004.hp2 others(11): Show |
intron_variant | MODIFIER | c.92+461T>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56965396 | |||||||
| chr1:56965398 | A | AGAGAGT | 7 | a0001c0001t0001g0047 a0001c0001t0001g0208 a0001c0001t0001g0210 others(4): Show |
11 | HG00280.hp1 HG00438.hp1 HG00642.hp2 others(8): Show |
intron_variant | MODIFIER | c.92+458_92+459insAC others(4): Show |
C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56965398 | |||||||
| chr1:56965398 | A | AGAGAGTG others(1): Show |
2 | a0001c0001t0001g0039 a0001c0001t0001g0040 |
4 | HG01346.hp1 HG01978.hp1 NA18963.hp1 others(1): Show |
intron_variant | MODIFIER | c.92+458_92+459insAC others(6): Show |
C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56965398 | |||||||
| chr1:56965398 | A | AGAGAGTG others(3): Show |
2 | a0001c0001t0001g0150 a0001c0001t0001g0151 |
2 | HG02630.hp2 NA18997.hp2 |
intron_variant | MODIFIER | c.92+458_92+459insAC others(8): Show |
C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56965398 | |||||||
| chr1:56965398 | A | AGAGAGTG others(5): Show |
1 | a0001c0001t0001g0149 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.92+458_92+459insAC others(10): Show |
C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56965398 | |||||||
| chr1:56965398 | A | AGAGAGTG others(7): Show |
2 | a0001c0001t0001g0094 a0001c0001t0002g0027 |
3 | HG00738.hp2 HG01261.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.92+458_92+459insAC others(12): Show |
C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56965398 | |||||||
| chr1:56965398 | A | AGAGAGTG others(9): Show |
1 | a0001c0001t0001g0086 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.92+458_92+459insAC others(14): Show |
C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56965398 | |||||||
| chr1:56965398 | A | AGAGAGTG others(11): Show |
7 | a0001c0001t0001g0077 a0001c0001t0001g0079 a0001c0001t0001g0082 others(4): Show |
7 | HG00597.hp1 HG00735.hp1 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.92+458_92+459insAC others(16): Show |
C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56965398 | |||||||
| chr1:56965398 | A | AGAGAGTG others(13): Show |
2 | a0001c0001t0002g0074 a0001c0001t0002g0075 |
2 | HG02027.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.92+458_92+459insAC others(18): Show |
C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56965398 | |||||||
| chr1:56965398 | A | AGAGAGTG others(15): Show |
2 | a0001c0001t0002g0072 a0001c0001t0002g0073 |
2 | NA18939.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.92+458_92+459insAC others(20): Show |
C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56965398 | |||||||
| chr1:56965398 | A | AGAGT | 6 | a0001c0001t0001g0046 a0001c0001t0001g0068 a0001c0001t0001g0204 others(3): Show |
7 | HG01109.hp1 HG01346.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.92+458_92+459insAC others(2): Show |
C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56965398 | |||||||
| chr1:56965398 | A | AGAGTGT | 11 | a0001c0001t0001g0025 a0001c0001t0001g0061 a0001c0001t0001g0062 others(8): Show |
13 | HG02145.hp2 HG02258.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.92+458_92+459insAC others(4): Show |
C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56965398 | |||||||
| chr1:56965398 | A | AGAGTGTG others(3): Show |
6 | a0001c0001t0001g0014 a0001c0001t0001g0144 a0001c0001t0001g0145 others(3): Show |
9 | HG00639.hp2 HG02300.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.92+458_92+459insAC others(8): Show |
C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56965398 | |||||||
| chr1:56965398 | A | AGAGTGTG others(5): Show |
1 | a0001c0001t0001g0093 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.92+458_92+459insAC others(10): Show |
C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56965398 | |||||||
| chr1:56965398 | A | AGAGTGTG others(7): Show |
1 | a0001c0001t0001g0085 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.92+458_92+459insAC others(12): Show |
C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56965398 | |||||||
| chr1:56965398 | A | AGT | 38 | a0001c0001t0001g0003 a0001c0001t0001g0041 a0001c0001t0001g0044 others(35): Show |
49 | HG00408.hp1 HG00733.hp1 HG00735.hp2 others(46): Show |
intron_variant | MODIFIER | c.92+457_92+458dupAC | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56965398 | |||||||
| chr1:56965398 | A | AGTGT | 20 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0160 others(17): Show |
30 | HG00544.hp1 HG00673.hp1 HG00673.hp2 others(27): Show |
intron_variant | MODIFIER | c.92+455_92+458dupAC others(2): Show |
C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56965398 | |||||||
| chr1:56965398 | A | AGTGTGTG others(1): Show |
56 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0016 others(53): Show |
79 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(76): Show |
intron_variant | MODIFIER | c.92+451_92+458dupAC others(6): Show |
C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56965398 | |||||||
| chr1:56965398 | A | AGTGTGTG others(3): Show |
5 | a0001c0001t0001g0089 a0001c0001t0002g0088 a0001c0001t0002g0090 others(2): Show |
5 | HG01884.hp1 HG01934.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.92+449_92+458dupAC others(8): Show |
C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56965398 | |||||||
| chr1:56965398 | A | AGTGTGTG others(5): Show |
2 | a0001c0001t0001g0083 a0001c0001t0001g0084 |
2 | HG02970.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.92+447_92+458dupAC others(10): Show |
C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56965398 | |||||||
| chr1:56965398 | A | T | 18 | a0001c0001t0001g0010 a0001c0001t0001g0026 a0001c0001t0001g0029 others(15): Show |
26 | HG01069.hp1 HG01070.hp1 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.92+459T>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56965398 | |||||||
| chr1:56965400 | T | A | 2 | a0001c0001t0002g0281 a0002c0002t0001g0280 |
2 | HG03209.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.92+457A>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56965400 | |||||||
| chr1:56965512 | TTCATGAA others(12): Show |
T | 11 | a0001c0001t0001g0025 a0001c0001t0001g0061 a0001c0001t0001g0062 others(8): Show |
13 | HG02055.hp1 HG02145.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.92+326_92+344delCA others(17): Show |
C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56965512 | |||||||
| chr1:56965578 | G | A | 4 | a0001c0001t0002g0058 a0001c0001t0002g0059 a0002c0002t0001g0283 others(1): Show |
6 | HG01070.hp1 HG01256.hp1 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.92+279C>T | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56965578 | |||||||
| chr1:56965589 | G | T | 1 | a0001c0001t0002g0071 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.92+268C>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56965589 | |||||||
| chr1:56965702 | A | G | 12 | a0001c0001t0001g0025 a0001c0001t0001g0061 a0001c0001t0001g0062 others(9): Show |
14 | HG02055.hp1 HG02145.hp2 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.92+155T>C | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56965702 | |||||||
| chr1:56965805 | C | T | 1 | a0001c0001t0002g0060 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.92+52G>A | C8B | ENSG00000021852.14 | transcript | ENST00000371237.9 | protein_coding | 1/11 | chr1 | 56965805 |