Search by Gene
| Item | Value |
|---|---|
| geneid | 64241 |
| ensemblid | ENSG00000143921.9 |
| hgncid | 13887 |
| symbol | ABCG8 |
| name | ATP binding cassette subfamily G member 8 |
| refseq_nuc | NM_022437.3 |
| refseq_prot | NP_071882.1 |
| ensembl_nuc | ENST00000272286.4 |
| ensembl_prot | ENSP00000272286.2 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 43838971 |
| end | 43882988 |
| strand | + |
| ver | v1.2 |
| region | chr2:43838971-43882988 |
| region5000 | chr2:43833971-43887988 |
| regionname0 | ABCG8_chr2_43838971_43882988 |
| regionname5000 | ABCG8_chr2_43833971_43887988 |
Multiple Alignments (by translate haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
Multiple Alignments (by aa haplotype frequency)
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 673 | 111 | 14 | 14 | 66 | 1 | 16 | ABCG8_chr2_43833971_43887988 | ABCG8 | MAGKA others(668): Show |
chr2 | 43833971 | 43887988 |
| a0002 | 0/0 | 673 | 78 | 23 | 20 | 22 | 4 | 9 | ABCG8_chr2_43833971_43887988 | ABCG8 | MAGKA others(668): Show |
chr2 | 43833971 | 43887988 |
| a0003 | 0/0 | 673 | 66 | 26 | 21 | 9 | 3 | 7 | ABCG8_chr2_43833971_43887988 | ABCG8 | MAGKA others(668): Show |
chr2 | 43833971 | 43887988 |
| a0004 | 1/1 | 673 | 12 | 2 | 6 | 0 | 1 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | MAGKA others(668): Show |
chr2 | 43833971 | 43887988 |
| a0005 | 0/0 | 673 | 12 | 0 | 9 | 0 | 1 | 2 | ABCG8_chr2_43833971_43887988 | ABCG8 | MAGKA others(668): Show |
chr2 | 43833971 | 43887988 |
| a0006 | 0/0 | 673 | 12 | 4 | 2 | 4 | 0 | 2 | ABCG8_chr2_43833971_43887988 | ABCG8 | MAGKA others(668): Show |
chr2 | 43833971 | 43887988 |
| a0007 | 0/0 | 673 | 7 | 6 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | MAGKA others(668): Show |
chr2 | 43833971 | 43887988 |
| a0008 | 0/0 | 673 | 5 | 5 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | MAGKA others(668): Show |
chr2 | 43833971 | 43887988 |
| a0009 | 0/0 | 673 | 4 | 4 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | MAGKA others(668): Show |
chr2 | 43833971 | 43887988 |
| a0010 | 0/0 | 673 | 3 | 0 | 2 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | MAGKA others(668): Show |
chr2 | 43833971 | 43887988 |
| a0011 | 0/0 | 673 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | MAGKA others(668): Show |
chr2 | 43833971 | 43887988 |
| a0012 | 0/0 | 673 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | MAGKA others(668): Show |
chr2 | 43833971 | 43887988 |
| a0013 | 0/0 | 673 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | MAGKA others(668): Show |
chr2 | 43833971 | 43887988 |
| a0014 | 0/0 | 673 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | MAGKA others(668): Show |
chr2 | 43833971 | 43887988 |
| a0015 | 0/0 | 673 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | MAGKA others(668): Show |
chr2 | 43833971 | 43887988 |
| a0016 | 0/0 | 673 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | MAGKA others(668): Show |
chr2 | 43833971 | 43887988 |
| a0017 | 0/0 | 673 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | MAGKA others(668): Show |
chr2 | 43833971 | 43887988 |
| a0018 | 0/0 | 673 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | MAGKA others(668): Show |
chr2 | 43833971 | 43887988 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 2019 | 102 | 12 | 11 | 66 | 1 | 12 | ABCG8_chr2_43833971_43887988 | ABCG8 | ATGGC others(2014): Show |
chr2 | 43833971 | 43887988 | ||
| a0001c0008 | 0/0 | 2019 | 9 | 2 | 3 | 0 | 0 | 4 | ABCG8_chr2_43833971_43887988 | ABCG8 | ATGGC others(2014): Show |
chr2 | 43833971 | 43887988 | ||
| a0002c0003 | 0/0 | 2019 | 49 | 14 | 12 | 16 | 2 | 5 | ABCG8_chr2_43833971_43887988 | ABCG8 | ATGGC others(2014): Show |
chr2 | 43833971 | 43887988 | ||
| a0002c0004 | 0/0 | 2019 | 27 | 9 | 8 | 5 | 2 | 3 | ABCG8_chr2_43833971_43887988 | ABCG8 | ATGGC others(2014): Show |
chr2 | 43833971 | 43887988 | ||
| a0002c0024 | 0/0 | 2019 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | ATGGC others(2014): Show |
chr2 | 43833971 | 43887988 | ||
| a0002c0026 | 0/0 | 2019 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | ATGGC others(2014): Show |
chr2 | 43833971 | 43887988 | ||
| a0003c0002 | 0/0 | 2019 | 51 | 18 | 16 | 9 | 3 | 5 | ABCG8_chr2_43833971_43887988 | ABCG8 | ATGGC others(2014): Show |
chr2 | 43833971 | 43887988 | ||
| a0003c0010 | 0/0 | 2019 | 4 | 1 | 1 | 0 | 0 | 2 | ABCG8_chr2_43833971_43887988 | ABCG8 | ATGGC others(2014): Show |
chr2 | 43833971 | 43887988 | ||
| a0003c0011 | 0/0 | 2019 | 4 | 4 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | ATGGC others(2014): Show |
chr2 | 43833971 | 43887988 | ||
| a0003c0014 | 0/0 | 2019 | 3 | 1 | 2 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | ATGGC others(2014): Show |
chr2 | 43833971 | 43887988 | ||
| a0003c0017 | 0/0 | 2019 | 2 | 0 | 2 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | ATGGC others(2014): Show |
chr2 | 43833971 | 43887988 | ||
| a0003c0021 | 0/0 | 2019 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | ATGGC others(2014): Show |
chr2 | 43833971 | 43887988 | ||
| a0003c0022 | 0/0 | 2019 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | ATGGC others(2014): Show |
chr2 | 43833971 | 43887988 | ||
| a0004c0006 | 1/1 | 2019 | 12 | 2 | 6 | 0 | 1 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | ATGGC others(2014): Show |
chr2 | 43833971 | 43887988 | ||
| a0005c0007 | 0/0 | 2019 | 12 | 0 | 9 | 0 | 1 | 2 | ABCG8_chr2_43833971_43887988 | ABCG8 | ATGGC others(2014): Show |
chr2 | 43833971 | 43887988 | ||
| a0006c0005 | 0/0 | 2019 | 12 | 4 | 2 | 4 | 0 | 2 | ABCG8_chr2_43833971_43887988 | ABCG8 | ATGGC others(2014): Show |
chr2 | 43833971 | 43887988 | ||
| a0007c0009 | 0/0 | 2019 | 6 | 5 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | ATGGC others(2014): Show |
chr2 | 43833971 | 43887988 | ||
| a0007c0020 | 0/0 | 2019 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | ATGGC others(2014): Show |
chr2 | 43833971 | 43887988 | ||
| a0008c0015 | 0/0 | 2019 | 2 | 2 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | ATGGC others(2014): Show |
chr2 | 43833971 | 43887988 | ||
| a0008c0016 | 0/0 | 2019 | 2 | 2 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | ATGGC others(2014): Show |
chr2 | 43833971 | 43887988 | ||
| a0008c0018 | 0/0 | 2019 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | ATGGC others(2014): Show |
chr2 | 43833971 | 43887988 | ||
| a0009c0012 | 0/0 | 2019 | 4 | 4 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | ATGGC others(2014): Show |
chr2 | 43833971 | 43887988 | ||
| a0010c0013 | 0/0 | 2019 | 3 | 0 | 2 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | ATGGC others(2014): Show |
chr2 | 43833971 | 43887988 | ||
| a0011c0023 | 0/0 | 2019 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | ATGGC others(2014): Show |
chr2 | 43833971 | 43887988 | ||
| a0012c0031 | 0/0 | 2019 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | ATGGC others(2014): Show |
chr2 | 43833971 | 43887988 | ||
| a0013c0029 | 0/0 | 2019 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | ATGGC others(2014): Show |
chr2 | 43833971 | 43887988 | ||
| a0014c0025 | 0/0 | 2019 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | ATGGC others(2014): Show |
chr2 | 43833971 | 43887988 | ||
| a0015c0028 | 0/0 | 2019 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | ATGGC others(2014): Show |
chr2 | 43833971 | 43887988 | ||
| a0016c0030 | 0/0 | 2019 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | ATGGC others(2014): Show |
chr2 | 43833971 | 43887988 | ||
| a0017c0019 | 0/0 | 2019 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | ATGGC others(2014): Show |
chr2 | 43833971 | 43887988 | ||
| a0018c0027 | 0/0 | 2019 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | ATGGC others(2014): Show |
chr2 | 43833971 | 43887988 |
| acthapid | grch38/chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 7182 | 24 | 0 | 5 | 14 | 1 | 4 | ABCG8_chr2_43833971_43887988 | ABCG8 | AAACA others(7177): Show |
chr2 | 43833971 | 43887988 |
| a0001c0001t0003 | 0/0 | 7180 | 19 | 0 | 1 | 18 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | AAACA others(7175): Show |
chr2 | 43833971 | 43887988 |
| a0001c0001t0007 | 0/0 | 7177 | 7 | 1 | 1 | 5 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | AAACA others(7172): Show |
chr2 | 43833971 | 43887988 |
| a0001c0001t0010 | 0/0 | 7182 | 6 | 0 | 0 | 6 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | AAACA others(7177): Show |
chr2 | 43833971 | 43887988 |
| a0001c0001t0011 | 0/0 | 7183 | 7 | 6 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | AAACA others(7178): Show |
chr2 | 43833971 | 43887988 |
| a0001c0001t0015 | 0/0 | 7181 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | AAACA others(7176): Show |
chr2 | 43833971 | 43887988 |
| a0001c0001t0016 | 0/0 | 7180 | 4 | 0 | 0 | 4 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | AAACA others(7175): Show |
chr2 | 43833971 | 43887988 |
| a0001c0001t0017 | 0/0 | 7183 | 4 | 0 | 0 | 4 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | AAACA others(7178): Show |
chr2 | 43833971 | 43887988 |
| a0001c0001t0029 | 0/0 | 7180 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | AAACA others(7175): Show |
chr2 | 43833971 | 43887988 |
| a0001c0001t0030 | 0/0 | 7182 | 2 | 0 | 0 | 2 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | AAACA others(7177): Show |
chr2 | 43833971 | 43887988 |
| a0001c0001t0031 | 0/0 | 7178 | 2 | 2 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | AAACA others(7173): Show |
chr2 | 43833971 | 43887988 |
| a0001c0001t0032 | 0/0 | 7182 | 2 | 0 | 0 | 2 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | AAACA others(7177): Show |
chr2 | 43833971 | 43887988 |
| a0001c0001t0033 | 0/0 | 7183 | 2 | 0 | 1 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | AAACA others(7178): Show |
chr2 | 43833971 | 43887988 |
| a0001c0001t0034 | 0/0 | 7183 | 2 | 0 | 0 | 2 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | AAACA others(7178): Show |
chr2 | 43833971 | 43887988 |
| a0001c0001t0035 | 0/0 | 7183 | 2 | 2 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | AAACA others(7178): Show |
chr2 | 43833971 | 43887988 |
| a0001c0001t0047 | 0/0 | 7182 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | AAACA others(7177): Show |
chr2 | 43833971 | 43887988 |
| a0001c0001t0048 | 0/0 | 7181 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | AAACA others(7176): Show |
chr2 | 43833971 | 43887988 |
| a0001c0001t0054 | 0/0 | 7180 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | AAACA others(7175): Show |
chr2 | 43833971 | 43887988 |
| a0001c0001t0055 | 0/0 | 7180 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | AAACA others(7175): Show |
chr2 | 43833971 | 43887988 |
| a0001c0001t0056 | 0/0 | 7182 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | AAACA others(7177): Show |
chr2 | 43833971 | 43887988 |
| a0001c0001t0057 | 0/0 | 7181 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | AAACA others(7176): Show |
chr2 | 43833971 | 43887988 |
| a0001c0001t0058 | 0/0 | 7182 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | AAACA others(7177): Show |
chr2 | 43833971 | 43887988 |
| a0001c0001t0059 | 0/0 | 7181 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | AAACA others(7176): Show |
chr2 | 43833971 | 43887988 |
| a0001c0001t0060 | 0/0 | 7182 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | AAACA others(7177): Show |
chr2 | 43833971 | 43887988 |
| a0001c0001t0062 | 0/0 | 7180 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | AAACA others(7175): Show |
chr2 | 43833971 | 43887988 |
| a0001c0001t0063 | 0/0 | 7182 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | AAACA others(7177): Show |
chr2 | 43833971 | 43887988 |
| a0001c0001t0065 | 0/0 | 7182 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | AAACA others(7177): Show |
chr2 | 43833971 | 43887988 |
| a0001c0001t0067 | 0/0 | 7182 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | AAACA others(7177): Show |
chr2 | 43833971 | 43887988 |
| a0001c0001t0068 | 0/0 | 7184 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | AAACA others(7179): Show |
chr2 | 43833971 | 43887988 |
| a0001c0001t0069 | 0/0 | 7180 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | AAACA others(7175): Show |
chr2 | 43833971 | 43887988 |
| a0001c0001t0070 | 0/0 | 7182 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | AAACA others(7177): Show |
chr2 | 43833971 | 43887988 |
| a0001c0001t0071 | 0/0 | 7183 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | AAACA others(7178): Show |
chr2 | 43833971 | 43887988 |
| a0001c0008t0008 | 0/0 | 7180 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | AAACA others(7175): Show |
chr2 | 43833971 | 43887988 |
| a0001c0008t0015 | 0/0 | 7181 | 4 | 0 | 1 | 0 | 0 | 3 | ABCG8_chr2_43833971_43887988 | ABCG8 | AAACA others(7176): Show |
chr2 | 43833971 | 43887988 |
| a0001c0008t0029 | 0/0 | 7180 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | AAACA others(7175): Show |
chr2 | 43833971 | 43887988 |
| a0001c0008t0050 | 0/0 | 7183 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | AAACA others(7178): Show |
chr2 | 43833971 | 43887988 |
| a0001c0008t0051 | 0/0 | 7182 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | AAACA others(7177): Show |
chr2 | 43833971 | 43887988 |
| a0001c0008t0073 | 0/0 | 7181 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | AAACA others(7176): Show |
chr2 | 43833971 | 43887988 |
| a0002c0003t0002 | 0/0 | 7177 | 10 | 3 | 4 | 2 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | AAACA others(7172): Show |
chr2 | 43833971 | 43887988 |
| a0002c0003t0004 | 0/0 | 7182 | 4 | 0 | 1 | 0 | 0 | 3 | ABCG8_chr2_43833971_43887988 | ABCG8 | AAACA others(7177): Show |
chr2 | 43833971 | 43887988 |
| a0002c0003t0005 | 0/0 | 7180 | 11 | 0 | 6 | 5 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | AAACA others(7175): Show |
chr2 | 43833971 | 43887988 |
| a0002c0003t0012 | 0/0 | 7181 | 2 | 2 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | AAACA others(7176): Show |
chr2 | 43833971 | 43887988 |
| a0002c0003t0013 | 0/0 | 7184 | 7 | 0 | 0 | 7 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | AAACA others(7179): Show |
chr2 | 43833971 | 43887988 |
| a0002c0003t0020 | 0/0 | 7182 | 1 | 0 | 0 | 0 | 1 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | AAACA others(7177): Show |
chr2 | 43833971 | 43887988 |
| a0002c0003t0027 | 0/0 | 7183 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | AAACA others(7178): Show |
chr2 | 43833971 | 43887988 |
| a0002c0003t0036 | 0/0 | 7180 | 2 | 2 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | AAACA others(7175): Show |
chr2 | 43833971 | 43887988 |
| a0002c0003t0039 | 0/0 | 7180 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | AAACA others(7175): Show |
chr2 | 43833971 | 43887988 |
| a0002c0003t0041 | 0/0 | 7181 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | AAACA others(7176): Show |
chr2 | 43833971 | 43887988 |
| a0002c0003t0090 | 0/0 | 7177 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | AAACA others(7172): Show |
chr2 | 43833971 | 43887988 |
| a0002c0003t0094 | 0/0 | 7182 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | AAACA others(7177): Show |
chr2 | 43833971 | 43887988 |
| a0002c0003t0096 | 0/0 | 7185 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | AAACA others(7180): Show |
chr2 | 43833971 | 43887988 |
| a0002c0003t0097 | 0/0 | 7176 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | AAACA others(7171): Show |
chr2 | 43833971 | 43887988 |
| a0002c0003t0098 | 0/0 | 7180 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | AAACA others(7175): Show |
chr2 | 43833971 | 43887988 |
| a0002c0003t0101 | 0/0 | 7183 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | AAACA others(7178): Show |
chr2 | 43833971 | 43887988 |
| a0002c0003t0103 | 0/0 | 7182 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | AAACA others(7177): Show |
chr2 | 43833971 | 43887988 |
| a0002c0003t0105 | 0/0 | 7183 | 1 | 0 | 0 | 0 | 1 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | AAACA others(7178): Show |
chr2 | 43833971 | 43887988 |
| a0002c0003t0107 | 0/0 | 7182 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | AAACA others(7177): Show |
chr2 | 43833971 | 43887988 |
| a0002c0004t0008 | 0/0 | 7180 | 7 | 3 | 3 | 0 | 1 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | AAACA others(7175): Show |
chr2 | 43833971 | 43887988 |
| a0002c0004t0009 | 0/0 | 7181 | 8 | 0 | 4 | 1 | 1 | 2 | ABCG8_chr2_43833971_43887988 | ABCG8 | AAACA others(7176): Show |
chr2 | 43833971 | 43887988 |
| a0002c0004t0014 | 0/0 | 7180 | 5 | 5 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | AAACA others(7175): Show |
chr2 | 43833971 | 43887988 |
| a0002c0004t0037 | 0/0 | 7182 | 2 | 0 | 1 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | AAACA others(7177): Show |
chr2 | 43833971 | 43887988 |
| a0002c0004t0038 | 0/0 | 7181 | 2 | 0 | 0 | 2 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | AAACA others(7176): Show |
chr2 | 43833971 | 43887988 |
| a0002c0004t0077 | 0/0 | 7181 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | AAACA others(7176): Show |
chr2 | 43833971 | 43887988 |
| a0002c0004t0078 | 0/0 | 7181 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | AAACA others(7176): Show |
chr2 | 43833971 | 43887988 |
| a0002c0004t0081 | 0/0 | 7183 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | AAACA others(7178): Show |
chr2 | 43833971 | 43887988 |
| a0002c0024t0108 | 0/0 | 7182 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | AAACA others(7177): Show |
chr2 | 43833971 | 43887988 |
| a0002c0026t0087 | 0/0 | 7182 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | AAACA others(7177): Show |
chr2 | 43833971 | 43887988 |
| a0003c0002t0001 | 0/0 | 7182 | 4 | 0 | 0 | 4 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | AAACA others(7177): Show |
chr2 | 43833971 | 43887988 |
| a0003c0002t0002 | 0/0 | 7177 | 9 | 1 | 7 | 0 | 1 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | AAACA others(7172): Show |
chr2 | 43833971 | 43887988 |
| a0003c0002t0004 | 0/0 | 7182 | 6 | 1 | 2 | 0 | 1 | 2 | ABCG8_chr2_43833971_43887988 | ABCG8 | AAACA others(7177): Show |
chr2 | 43833971 | 43887988 |
| a0003c0002t0005 | 0/0 | 7180 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | AAACA others(7175): Show |
chr2 | 43833971 | 43887988 |
| a0003c0002t0008 | 0/0 | 7180 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | AAACA others(7175): Show |
chr2 | 43833971 | 43887988 |
| a0003c0002t0010 | 0/0 | 7182 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | AAACA others(7177): Show |
chr2 | 43833971 | 43887988 |
| a0003c0002t0018 | 0/0 | 7177 | 4 | 2 | 2 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | AAACA others(7172): Show |
chr2 | 43833971 | 43887988 |
| a0003c0002t0019 | 0/0 | 7182 | 4 | 3 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | AAACA others(7177): Show |
chr2 | 43833971 | 43887988 |
| a0003c0002t0021 | 0/0 | 7180 | 3 | 3 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | AAACA others(7175): Show |
chr2 | 43833971 | 43887988 |
| a0003c0002t0026 | 0/0 | 7178 | 3 | 1 | 2 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | AAACA others(7173): Show |
chr2 | 43833971 | 43887988 |
| a0003c0002t0027 | 0/0 | 7183 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | AAACA others(7178): Show |
chr2 | 43833971 | 43887988 |
| a0003c0002t0039 | 0/0 | 7180 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | AAACA others(7175): Show |
chr2 | 43833971 | 43887988 |
| a0003c0002t0042 | 0/0 | 7176 | 2 | 2 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | AAACA others(7171): Show |
chr2 | 43833971 | 43887988 |
| a0003c0002t0064 | 0/0 | 7183 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | AAACA others(7178): Show |
chr2 | 43833971 | 43887988 |
| a0003c0002t0075 | 0/0 | 7183 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | AAACA others(7178): Show |
chr2 | 43833971 | 43887988 |
| a0003c0002t0076 | 0/0 | 7182 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | AAACA others(7177): Show |
chr2 | 43833971 | 43887988 |
| a0003c0002t0089 | 0/0 | 7183 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | AAACA others(7178): Show |
chr2 | 43833971 | 43887988 |
| a0003c0002t0092 | 0/0 | 7181 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | AAACA others(7176): Show |
chr2 | 43833971 | 43887988 |
| a0003c0002t0093 | 0/0 | 7182 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | AAACA others(7177): Show |
chr2 | 43833971 | 43887988 |
| a0003c0002t0095 | 0/0 | 7183 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | AAACA others(7178): Show |
chr2 | 43833971 | 43887988 |
| a0003c0002t0100 | 0/0 | 7176 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | AAACA others(7171): Show |
chr2 | 43833971 | 43887988 |
| a0003c0002t0102 | 0/0 | 7180 | 1 | 0 | 0 | 0 | 1 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | AAACA others(7175): Show |
chr2 | 43833971 | 43887988 |
| a0003c0002t0104 | 0/0 | 7182 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | AAACA others(7177): Show |
chr2 | 43833971 | 43887988 |
| a0003c0002t0106 | 0/0 | 7182 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | AAACA others(7177): Show |
chr2 | 43833971 | 43887988 |
| a0003c0010t0020 | 0/0 | 7182 | 3 | 0 | 1 | 0 | 0 | 2 | ABCG8_chr2_43833971_43887988 | ABCG8 | AAACA others(7177): Show |
chr2 | 43833971 | 43887988 |
| a0003c0010t0110 | 0/0 | 7181 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | AAACA others(7176): Show |
chr2 | 43833971 | 43887988 |
| a0003c0011t0012 | 0/0 | 7181 | 3 | 3 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | AAACA others(7176): Show |
chr2 | 43833971 | 43887988 |
| a0003c0011t0091 | 0/0 | 7182 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | AAACA others(7177): Show |
chr2 | 43833971 | 43887988 |
| a0003c0014t0043 | 0/0 | 7176 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | AAACA others(7171): Show |
chr2 | 43833971 | 43887988 |
| a0003c0014t0079 | 0/0 | 7180 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | AAACA others(7175): Show |
chr2 | 43833971 | 43887988 |
| a0003c0014t0080 | 0/0 | 7180 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | AAACA others(7175): Show |
chr2 | 43833971 | 43887988 |
| a0003c0017t0007 | 0/0 | 7177 | 2 | 0 | 2 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | AAACA others(7172): Show |
chr2 | 43833971 | 43887988 |
| a0003c0021t0007 | 0/0 | 7177 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | AAACA others(7172): Show |
chr2 | 43833971 | 43887988 |
| a0003c0022t0014 | 0/0 | 7180 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | AAACA others(7175): Show |
chr2 | 43833971 | 43887988 |
| a0004c0006t0024 | 0/0 | 7180 | 3 | 0 | 3 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | AAACA others(7175): Show |
chr2 | 43833971 | 43887988 |
| a0004c0006t0025 | 1/0 | 7180 | 3 | 1 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | AAACA others(7175): Show |
chr2 | 43833971 | 43887988 |
| a0004c0006t0040 | 0/0 | 7180 | 2 | 0 | 2 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | AAACA others(7175): Show |
chr2 | 43833971 | 43887988 |
| a0004c0006t0082 | 0/0 | 7181 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | AAACA others(7176): Show |
chr2 | 43833971 | 43887988 |
| a0004c0006t0083 | 0/0 | 7180 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | AAACA others(7175): Show |
chr2 | 43833971 | 43887988 |
| a0004c0006t0085 | 0/0 | 7180 | 1 | 0 | 0 | 0 | 1 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | AAACA others(7175): Show |
chr2 | 43833971 | 43887988 |
| a0004c0006t0086 | 0/1 | 7180 | 1 | 0 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | AAACA others(7175): Show |
chr2 | 43833971 | 43887988 |
| a0005c0007t0006 | 0/0 | 7180 | 10 | 0 | 8 | 0 | 1 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | AAACA others(7175): Show |
chr2 | 43833971 | 43887988 |
| a0005c0007t0052 | 0/0 | 7180 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | AAACA others(7175): Show |
chr2 | 43833971 | 43887988 |
| a0005c0007t0053 | 0/0 | 7181 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | AAACA others(7176): Show |
chr2 | 43833971 | 43887988 |
| a0006c0005t0002 | 0/0 | 7177 | 2 | 1 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | AAACA others(7172): Show |
chr2 | 43833971 | 43887988 |
| a0006c0005t0004 | 0/0 | 7182 | 7 | 3 | 0 | 3 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | AAACA others(7177): Show |
chr2 | 43833971 | 43887988 |
| a0006c0005t0027 | 0/0 | 7183 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | AAACA others(7178): Show |
chr2 | 43833971 | 43887988 |
| a0006c0005t0041 | 0/0 | 7181 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | AAACA others(7176): Show |
chr2 | 43833971 | 43887988 |
| a0006c0005t0088 | 0/0 | 7180 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | AAACA others(7175): Show |
chr2 | 43833971 | 43887988 |
| a0007c0009t0022 | 0/0 | 7182 | 3 | 3 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | AAACA others(7177): Show |
chr2 | 43833971 | 43887988 |
| a0007c0009t0028 | 0/0 | 7182 | 2 | 2 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | AAACA others(7177): Show |
chr2 | 43833971 | 43887988 |
| a0007c0009t0049 | 0/0 | 7180 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | AAACA others(7175): Show |
chr2 | 43833971 | 43887988 |
| a0007c0020t0061 | 0/0 | 7176 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | AAACA others(7171): Show |
chr2 | 43833971 | 43887988 |
| a0008c0015t0012 | 0/0 | 7181 | 2 | 2 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | AAACA others(7176): Show |
chr2 | 43833971 | 43887988 |
| a0008c0016t0044 | 0/0 | 7176 | 2 | 2 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | AAACA others(7171): Show |
chr2 | 43833971 | 43887988 |
| a0008c0018t0002 | 0/0 | 7177 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | AAACA others(7172): Show |
chr2 | 43833971 | 43887988 |
| a0009c0012t0023 | 0/0 | 7176 | 3 | 3 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | AAACA others(7171): Show |
chr2 | 43833971 | 43887988 |
| a0009c0012t0072 | 0/0 | 7177 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | AAACA others(7172): Show |
chr2 | 43833971 | 43887988 |
| a0010c0013t0002 | 0/0 | 7177 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | AAACA others(7172): Show |
chr2 | 43833971 | 43887988 |
| a0010c0013t0005 | 0/0 | 7180 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | AAACA others(7175): Show |
chr2 | 43833971 | 43887988 |
| a0010c0013t0099 | 0/0 | 7177 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | AAACA others(7172): Show |
chr2 | 43833971 | 43887988 |
| a0011c0023t0084 | 0/0 | 7180 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | AAACA others(7175): Show |
chr2 | 43833971 | 43887988 |
| a0012c0031t0045 | 0/0 | 7181 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | AAACA others(7176): Show |
chr2 | 43833971 | 43887988 |
| a0013c0029t0066 | 0/0 | 7182 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | AAACA others(7177): Show |
chr2 | 43833971 | 43887988 |
| a0014c0025t0074 | 0/0 | 7180 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | AAACA others(7175): Show |
chr2 | 43833971 | 43887988 |
| a0015c0028t0043 | 0/0 | 7176 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | AAACA others(7171): Show |
chr2 | 43833971 | 43887988 |
| a0016c0030t0046 | 0/0 | 7181 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | AAACA others(7176): Show |
chr2 | 43833971 | 43887988 |
| a0017c0019t0109 | 0/0 | 7183 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | AAACA others(7178): Show |
chr2 | 43833971 | 43887988 |
| a0018c0027t0005 | 0/0 | 7180 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | AAACA others(7175): Show |
chr2 | 43833971 | 43887988 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0001c0001t0003g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0001c0001t0003g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0001c0001t0003g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0001c0001t0003g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0001c0001t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0001c0001t0003g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0001c0001t0003g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0001c0001t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0001c0001t0003g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0001c0001t0003g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0001c0001t0003g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0001c0001t0003g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0001c0001t0003g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0001c0001t0003g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0001c0001t0003g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0001c0001t0003g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0001c0001t0003g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0001c0001t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0001c0001t0007g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0001c0001t0007g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0001c0001t0007g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0001c0001t0007g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0001c0001t0007g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0001c0001t0007g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0001c0001t0007g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0001c0001t0010g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0001c0001t0010g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0001c0001t0010g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0001c0001t0010g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0001c0001t0010g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0001c0001t0010g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0001c0001t0011g0011 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0001c0001t0011g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0001c0001t0011g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0001c0001t0011g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0001c0001t0011g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0001c0001t0015g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0001c0001t0016g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0001c0001t0016g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0001c0001t0017g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0001c0001t0017g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0001c0001t0017g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0001c0001t0017g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0001c0001t0029g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0001c0001t0030g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0001c0001t0030g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0001c0001t0031g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0001c0001t0031g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0001c0001t0032g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0001c0001t0032g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0001c0001t0033g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0001c0001t0033g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0001c0001t0034g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0001c0001t0034g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0001c0001t0035g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0001c0001t0035g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0001c0001t0047g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0001c0001t0048g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0001c0001t0054g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0001c0001t0055g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0001c0001t0056g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0001c0001t0057g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0001c0001t0058g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0001c0001t0059g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0001c0001t0060g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0001c0001t0062g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0001c0001t0063g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0001c0001t0065g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0001c0001t0067g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0001c0001t0068g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0001c0001t0069g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0001c0001t0070g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0001c0001t0071g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0001c0008t0008g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0001c0008t0015g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0001c0008t0015g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0001c0008t0015g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0001c0008t0015g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0001c0008t0029g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0001c0008t0050g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0001c0008t0051g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0001c0008t0073g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0002c0003t0002g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0002c0003t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0002c0003t0002g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0002c0003t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0002c0003t0002g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0002c0003t0002g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0002c0003t0002g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0002c0003t0002g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0002c0003t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0002c0003t0002g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0002c0003t0004g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0002c0003t0004g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0002c0003t0004g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0002c0003t0004g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0002c0003t0005g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0002c0003t0005g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0002c0003t0005g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0002c0003t0005g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0002c0003t0005g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0002c0003t0005g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0002c0003t0005g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0002c0003t0005g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0002c0003t0005g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0002c0003t0005g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0002c0003t0005g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0002c0003t0012g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0002c0003t0012g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0002c0003t0013g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0002c0003t0013g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0002c0003t0013g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0002c0003t0013g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0002c0003t0013g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0002c0003t0020g0252 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0002c0003t0027g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0002c0003t0036g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0002c0003t0039g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0002c0003t0041g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0002c0003t0090g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0002c0003t0094g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0002c0003t0096g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0002c0003t0097g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0002c0003t0098g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0002c0003t0101g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0002c0003t0103g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0002c0003t0105g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0002c0003t0107g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0002c0004t0008g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0002c0004t0008g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0002c0004t0008g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0002c0004t0008g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0002c0004t0008g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0002c0004t0008g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0002c0004t0008g0272 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0002c0004t0009g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0002c0004t0009g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0002c0004t0009g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0002c0004t0009g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0002c0004t0009g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0002c0004t0009g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0002c0004t0009g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0002c0004t0009g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0002c0004t0014g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0002c0004t0014g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0002c0004t0014g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0002c0004t0014g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0002c0004t0014g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0002c0004t0037g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0002c0004t0037g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0002c0004t0038g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0002c0004t0077g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0002c0004t0078g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0002c0004t0081g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0002c0024t0108g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0002c0026t0087g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0003c0002t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0003c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0003c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0003c0002t0002g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0003c0002t0002g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0003c0002t0002g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0003c0002t0002g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0003c0002t0002g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0003c0002t0002g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0003c0002t0002g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0003c0002t0002g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0003c0002t0002g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0003c0002t0004g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0003c0002t0004g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0003c0002t0004g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0003c0002t0004g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0003c0002t0004g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0003c0002t0004g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0003c0002t0005g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0003c0002t0008g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0003c0002t0010g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0003c0002t0018g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0003c0002t0018g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0003c0002t0018g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0003c0002t0019g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0003c0002t0019g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0003c0002t0019g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0003c0002t0019g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0003c0002t0021g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0003c0002t0021g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0003c0002t0021g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0003c0002t0026g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0003c0002t0026g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0003c0002t0026g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0003c0002t0027g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0003c0002t0039g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0003c0002t0042g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0003c0002t0064g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0003c0002t0075g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0003c0002t0076g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0003c0002t0089g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0003c0002t0092g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0003c0002t0093g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0003c0002t0095g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0003c0002t0100g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0003c0002t0102g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0003c0002t0104g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0003c0002t0106g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0003c0010t0020g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0003c0010t0020g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0003c0010t0020g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0003c0010t0110g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0003c0011t0012g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0003c0011t0012g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0003c0011t0091g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0003c0014t0043g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0003c0014t0079g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0003c0014t0080g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0003c0017t0007g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0003c0021t0007g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0003c0022t0014g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0004c0006t0024g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0004c0006t0024g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0004c0006t0024g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0004c0006t0025g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0004c0006t0025g0273 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0004c0006t0025g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0004c0006t0040g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0004c0006t0040g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0004c0006t0082g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0004c0006t0083g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0004c0006t0085g0268 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0004c0006t0086g0285 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0005c0007t0006g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0005c0007t0006g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0005c0007t0006g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0005c0007t0006g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0005c0007t0006g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0005c0007t0006g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0005c0007t0006g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0005c0007t0006g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0005c0007t0006g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0005c0007t0052g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0005c0007t0053g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0006c0005t0002g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0006c0005t0002g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0006c0005t0004g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0006c0005t0004g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0006c0005t0004g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0006c0005t0004g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0006c0005t0004g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0006c0005t0004g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0006c0005t0027g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0006c0005t0041g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0006c0005t0088g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0007c0009t0022g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0007c0009t0022g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0007c0009t0028g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0007c0009t0028g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0007c0009t0049g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0007c0020t0061g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0008c0015t0012g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0008c0016t0044g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0008c0016t0044g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0008c0018t0002g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0009c0012t0023g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0009c0012t0023g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0009c0012t0023g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0009c0012t0072g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0010c0013t0002g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0010c0013t0005g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0010c0013t0099g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0011c0023t0084g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0012c0031t0045g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0013c0029t0066g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0014c0025t0074g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0015c0028t0043g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0016c0030t0046g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0017c0019t0109g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| a0018c0027t0005g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| sampleid | haplotypeid | ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0008 | EUR | GBR | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG00099 | hp2 | a0003 | c0002 | t0002 | g0264 | EUR | GBR | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG00280 | hp1 | a0005 | c0007 | t0006 | g0064 | EUR | FIN | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG00280 | hp2 | a0002 | c0003 | t0020 | g0252 | EUR | FIN | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG00323 | hp1 | a0002 | c0004 | t0008 | g0272 | EUR | FIN | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG00323 | hp2 | a0004 | c0006 | t0085 | g0268 | EUR | FIN | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG00438 | hp1 | a0006 | c0005 | t0027 | g0220 | EAS | CHS | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG00438 | hp2 | a0001 | c0001 | t0016 | g0106 | EAS | CHS | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG00558 | hp1 | a0001 | c0001 | t0007 | g0089 | EAS | CHS | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | CHS | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG00597 | hp1 | a0001 | c0001 | t0030 | g0117 | EAS | CHS | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG00597 | hp2 | a0001 | c0001 | t0003 | g0134 | EAS | CHS | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG00621 | hp1 | a0002 | c0003 | t0041 | g0169 | EAS | CHS | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG00621 | hp2 | a0001 | c0001 | t0007 | g0010 | EAS | CHS | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG00639 | hp1 | a0001 | c0001 | t0062 | g0050 | AMR | PUR | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG00639 | hp2 | a0003 | c0002 | t0002 | g0175 | AMR | PUR | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG00642 | hp1 | a0003 | c0014 | t0079 | g0276 | AMR | PUR | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG00642 | hp2 | a0003 | c0017 | t0007 | g0014 | AMR | PUR | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG00673 | hp1 | a0001 | c0001 | t0007 | g0145 | EAS | CHS | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG00673 | hp2 | a0001 | c0001 | t0003 | g0103 | EAS | CHS | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG00733 | hp1 | a0005 | c0007 | t0006 | g0148 | AMR | PUR | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG00733 | hp2 | a0003 | c0002 | t0039 | g0279 | AMR | PUR | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG00735 | hp1 | a0003 | c0002 | t0002 | g0284 | AMR | PUR | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG00735 | hp2 | a0005 | c0007 | t0052 | g0013 | AMR | PUR | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG00738 | hp1 | a0002 | c0003 | t0002 | g0019 | AMR | PUR | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG00738 | hp2 | a0002 | c0004 | t0008 | g0182 | AMR | PUR | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG00741 | hp1 | a0003 | c0014 | t0080 | g0288 | AMR | PUR | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG00741 | hp2 | a0006 | c0005 | t0002 | g0260 | AMR | PUR | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG01069 | hp1 | a0005 | c0007 | t0006 | g0006 | AMR | PUR | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG01069 | hp2 | a0002 | c0004 | t0009 | g0262 | AMR | PUR | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG01070 | hp1 | a0002 | c0003 | t0002 | g0200 | AMR | PUR | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG01070 | hp2 | a0003 | c0002 | t0002 | g0282 | AMR | PUR | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG01071 | hp1 | a0005 | c0007 | t0006 | g0006 | AMR | PUR | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG01071 | hp2 | a0003 | c0002 | t0002 | g0290 | AMR | PUR | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG01074 | hp1 | a0003 | c0002 | t0018 | g0015 | AMR | PUR | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG01074 | hp2 | a0003 | c0002 | t0002 | g0287 | AMR | PUR | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG01081 | hp1 | a0005 | c0007 | t0006 | g0013 | AMR | PUR | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0070 | AMR | PUR | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG01099 | hp1 | a0003 | c0002 | t0018 | g0015 | AMR | PUR | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG01099 | hp2 | a0003 | c0017 | t0007 | g0014 | AMR | PUR | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG01106 | hp1 | a0002 | c0003 | t0005 | g0201 | AMR | PUR | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG01106 | hp2 | a0001 | c0001 | t0011 | g0011 | AMR | PUR | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG01109 | hp1 | a0002 | c0004 | t0008 | g0271 | AMR | PUR | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG01109 | hp2 | a0003 | c0002 | t0019 | g0163 | AMR | PUR | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG01167 | hp1 | a0005 | c0007 | t0006 | g0143 | AMR | PUR | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG01167 | hp2 | a0003 | c0002 | t0002 | g0283 | AMR | PUR | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG01168 | hp1 | a0005 | c0007 | t0006 | g0127 | AMR | PUR | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG01168 | hp2 | a0004 | c0006 | t0024 | g0043 | AMR | PUR | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG01169 | hp1 | a0005 | c0007 | t0006 | g0055 | AMR | PUR | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG01169 | hp2 | a0003 | c0002 | t0002 | g0275 | AMR | PUR | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG01175 | hp1 | a0003 | c0002 | t0004 | g0267 | AMR | PUR | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG01175 | hp2 | a0003 | c0002 | t0026 | g0269 | AMR | PUR | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG01192 | hp1 | a0003 | c0010 | t0020 | g0038 | AMR | PUR | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG01192 | hp2 | a0001 | c0008 | t0015 | g0144 | AMR | PUR | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG01255 | hp1 | a0004 | c0006 | t0083 | g0062 | AMR | CLM | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG01255 | hp2 | a0001 | c0008 | t0051 | g0141 | AMR | CLM | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG01256 | hp1 | a0002 | c0004 | t0009 | g0187 | AMR | CLM | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG01256 | hp2 | a0003 | c0002 | t0100 | g0265 | AMR | CLM | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG01261 | hp1 | a0002 | c0003 | t0002 | g0231 | AMR | CLM | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG01261 | hp2 | a0004 | c0006 | t0024 | g0263 | AMR | CLM | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG01346 | hp1 | a0004 | c0006 | t0040 | g0254 | AMR | CLM | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG01346 | hp2 | a0007 | c0009 | t0049 | g0031 | AMR | CLM | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG01361 | hp1 | a0004 | c0006 | t0024 | g0289 | AMR | CLM | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG01361 | hp2 | a0001 | c0001 | t0033 | g0008 | AMR | CLM | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG01433 | hp1 | a0002 | c0004 | t0009 | g0225 | AMR | CLM | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG01433 | hp2 | a0003 | c0002 | t0026 | g0164 | AMR | CLM | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG01496 | hp1 | a0001 | c0008 | t0008 | g0274 | AMR | CLM | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG01496 | hp2 | a0002 | c0004 | t0009 | g0188 | AMR | CLM | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG01515 | hp1 | a0003 | c0002 | t0004 | g0208 | EUR | IBS | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG01515 | hp2 | a0002 | c0004 | t0009 | g0185 | EUR | IBS | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG01884 | hp1 | a0002 | c0003 | t0101 | g0178 | AFR | ACB | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG01884 | hp2 | a0003 | c0002 | t0093 | g0161 | AFR | ACB | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG01891 | hp1 | a0004 | c0006 | t0025 | g0277 | AFR | ACB | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG01891 | hp2 | a0002 | c0004 | t0014 | g0258 | AFR | ACB | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG01928 | hp1 | a0002 | c0003 | t0005 | g0195 | AMR | PEL | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | PEL | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG01934 | hp1 | a0001 | c0001 | t0003 | g0130 | AMR | PEL | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG01934 | hp2 | a0001 | c0001 | t0071 | g0108 | AMR | PEL | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG01943 | hp1 | a0010 | c0013 | t0002 | g0167 | AMR | PEL | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG01943 | hp2 | a0002 | c0003 | t0005 | g0203 | AMR | PEL | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG01952 | hp1 | a0002 | c0003 | t0004 | g0248 | AMR | PEL | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG01952 | hp2 | a0002 | c0004 | t0037 | g0247 | AMR | PEL | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG01975 | hp1 | a0002 | c0003 | t0005 | g0202 | AMR | PEL | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG01975 | hp2 | a0010 | c0013 | t0005 | g0168 | AMR | PEL | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG01978 | hp1 | a0003 | c0002 | t0004 | g0286 | AMR | PEL | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG01978 | hp2 | a0006 | c0005 | t0088 | g0246 | AMR | PEL | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG01981 | hp1 | a0004 | c0006 | t0040 | g0241 | AMR | PEL | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG01981 | hp2 | a0002 | c0004 | t0008 | g0270 | AMR | PEL | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG01993 | hp2 | a0011 | c0023 | t0084 | g0206 | AMR | PEL | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG02015 | hp1 | a0002 | c0003 | t0002 | g0197 | EAS | KHV | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG02015 | hp2 | a0001 | c0001 | t0010 | g0060 | EAS | KHV | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG02027 | hp1 | a0001 | c0001 | t0003 | g0122 | EAS | KHV | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG02027 | hp2 | a0001 | c0001 | t0030 | g0119 | EAS | KHV | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG02040 | hp1 | a0001 | c0001 | t0003 | g0114 | EAS | KHV | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG02040 | hp2 | a0001 | c0001 | t0007 | g0118 | EAS | KHV | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG02055 | hp1 | a0001 | c0008 | t0050 | g0073 | AFR | ACB | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG02055 | hp2 | a0002 | c0003 | t0097 | g0256 | AFR | ACB | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG02056 | hp1 | a0001 | c0001 | t0003 | g0111 | EAS | KHV | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG02056 | hp2 | a0001 | c0001 | t0017 | g0132 | EAS | KHV | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG02074 | hp1 | a0001 | c0001 | t0057 | g0010 | EAS | KHV | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG02074 | hp2 | a0006 | c0005 | t0004 | g0221 | EAS | KHV | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | KHV | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG02080 | hp2 | a0001 | c0001 | t0017 | g0128 | EAS | KHV | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG02083 | hp1 | a0002 | c0026 | t0087 | g0198 | EAS | KHV | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG02083 | hp2 | a0001 | c0001 | t0047 | g0113 | EAS | KHV | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG02132 | hp1 | a0006 | c0005 | t0004 | g0023 | EAS | KHV | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG02132 | hp2 | a0001 | c0001 | t0003 | g0153 | EAS | KHV | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG02135 | hp1 | a0001 | c0001 | t0003 | g0104 | EAS | KHV | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG02135 | hp2 | a0001 | c0001 | t0034 | g0079 | EAS | KHV | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG02148 | hp1 | a0002 | c0003 | t0027 | g0235 | AMR | PEL | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG02148 | hp2 | a0005 | c0007 | t0006 | g0109 | AMR | PEL | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG02165 | hp1 | a0006 | c0005 | t0004 | g0023 | EAS | CDX | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | CDX | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG02257 | hp1 | a0003 | c0002 | t0018 | g0159 | AFR | ACB | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG02257 | hp2 | a0002 | c0003 | t0002 | g0044 | AFR | ACB | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG02280 | hp1 | a0003 | c0002 | t0018 | g0158 | AFR | ACB | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG02280 | hp2 | a0004 | c0006 | t0082 | g0281 | AFR | ACB | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG02293 | hp1 | a0002 | c0003 | t0005 | g0204 | AMR | PEL | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0072 | AMR | PEL | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG02300 | hp1 | a0002 | c0003 | t0005 | g0257 | AMR | PEL | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | PEL | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG02451 | hp1 | a0001 | c0001 | t0011 | g0012 | AFR | ACB | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG02451 | hp2 | a0003 | c0021 | t0007 | g0030 | AFR | ACB | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG02572 | hp1 | a0001 | c0001 | t0011 | g0125 | AFR | GWD | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG02572 | hp2 | a0002 | c0003 | t0096 | g0184 | AFR | GWD | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG02602 | hp1 | a0002 | c0003 | t0107 | g0186 | SAS | PJL | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG02602 | hp2 | a0013 | c0029 | t0066 | g0126 | SAS | PJL | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG02622 | hp1 | a0003 | c0002 | t0021 | g0149 | AFR | GWD | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG02622 | hp2 | a0002 | c0004 | t0078 | g0018 | AFR | GWD | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG02630 | hp1 | a0007 | c0009 | t0028 | g0033 | AFR | GWD | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG02630 | hp2 | a0002 | c0004 | t0014 | g0212 | AFR | GWD | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG02647 | hp1 | a0014 | c0025 | t0074 | g0156 | AFR | GWD | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG02647 | hp2 | a0003 | c0011 | t0012 | g0001 | AFR | GWD | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG02683 | hp1 | a0002 | c0003 | t0002 | g0234 | SAS | PJL | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG02683 | hp2 | a0001 | c0001 | t0029 | g0046 | SAS | PJL | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG02698 | hp1 | a0003 | c0002 | t0027 | g0280 | SAS | PJL | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG02698 | hp2 | a0003 | c0002 | t0008 | g0176 | SAS | PJL | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG02717 | hp1 | a0003 | c0002 | t0104 | g0216 | AFR | GWD | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG02717 | hp2 | a0015 | c0028 | t0043 | g0291 | AFR | GWD | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG02723 | hp1 | a0001 | c0001 | t0011 | g0011 | AFR | GWD | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG02723 | hp2 | a0003 | c0002 | t0019 | g0157 | AFR | GWD | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0098 | SAS | PJL | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG02735 | hp2 | a0002 | c0004 | t0077 | g0226 | SAS | PJL | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG02738 | hp1 | a0002 | c0004 | t0009 | g0251 | SAS | PJL | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG02738 | hp2 | a0001 | c0008 | t0015 | g0074 | SAS | PJL | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG02809 | hp1 | a0002 | c0003 | t0090 | g0035 | AFR | GWD | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG02809 | hp2 | a0003 | c0002 | t0042 | g0016 | AFR | GWD | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG02818 | hp1 | a0003 | c0002 | t0002 | g0209 | AFR | GWD | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG02818 | hp2 | a0003 | c0022 | t0014 | g0261 | AFR | GWD | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG02886 | hp1 | a0003 | c0002 | t0095 | g0242 | AFR | GWD | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG02886 | hp2 | a0001 | c0001 | t0011 | g0124 | AFR | GWD | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG02895 | hp1 | a0001 | c0001 | t0035 | g0053 | AFR | GWD | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG02895 | hp2 | a0003 | c0010 | t0110 | g0039 | AFR | GWD | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG02896 | hp1 | a0007 | c0009 | t0028 | g0034 | AFR | GWD | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG02896 | hp2 | a0008 | c0016 | t0044 | g0193 | AFR | GWD | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG02897 | hp1 | a0008 | c0016 | t0044 | g0192 | AFR | GWD | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG02897 | hp2 | a0001 | c0001 | t0035 | g0054 | AFR | GWD | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG02922 | hp1 | a0002 | c0004 | t0008 | g0181 | AFR | ESN | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG02922 | hp2 | a0002 | c0003 | t0002 | g0255 | AFR | ESN | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG02965 | hp1 | a0002 | c0003 | t0012 | g0147 | AFR | ESN | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG02965 | hp2 | a0001 | c0001 | t0011 | g0123 | AFR | ESN | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG02976 | hp1 | a0003 | c0002 | t0021 | g0150 | AFR | ESN | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG02976 | hp2 | a0002 | c0003 | t0012 | g0177 | AFR | ESN | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0097 | SAS | PJL | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG03017 | hp2 | a0016 | c0030 | t0046 | g0083 | SAS | PJL | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG03041 | hp1 | a0003 | c0002 | t0019 | g0063 | AFR | GWD | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG03041 | hp2 | a0002 | c0003 | t0039 | g0170 | AFR | GWD | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG03098 | hp1 | a0009 | c0012 | t0072 | g0024 | AFR | MSL | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG03098 | hp2 | a0006 | c0005 | t0004 | g0219 | AFR | MSL | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG03130 | hp1 | a0003 | c0011 | t0012 | g0001 | AFR | ESN | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG03130 | hp2 | a0001 | c0001 | t0007 | g0057 | AFR | ESN | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG03195 | hp1 | a0001 | c0001 | t0059 | g0133 | AFR | ESN | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG03195 | hp2 | a0017 | c0019 | t0109 | g0215 | AFR | ESN | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG03209 | hp1 | a0009 | c0012 | t0023 | g0028 | AFR | MSL | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG03209 | hp2 | a0006 | c0005 | t0004 | g0259 | AFR | MSL | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG03225 | hp1 | a0002 | c0004 | t0014 | g0179 | AFR | MSL | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG03225 | hp2 | a0003 | c0002 | t0092 | g0040 | AFR | MSL | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG03453 | hp1 | a0003 | c0002 | t0042 | g0016 | AFR | MSL | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG03453 | hp2 | a0002 | c0004 | t0014 | g0211 | AFR | MSL | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG03490 | hp1 | a0003 | c0010 | t0020 | g0036 | SAS | PJL | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG03490 | hp2 | a0001 | c0008 | t0015 | g0077 | SAS | PJL | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG03491 | hp1 | a0003 | c0002 | t0004 | g0266 | SAS | PJL | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG03491 | hp2 | a0006 | c0005 | t0004 | g0218 | SAS | PJL | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG03492 | hp1 | a0003 | c0010 | t0020 | g0037 | SAS | PJL | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG03492 | hp2 | a0003 | c0002 | t0004 | g0278 | SAS | PJL | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG03516 | hp1 | a0008 | c0018 | t0002 | g0174 | AFR | ESN | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG03516 | hp2 | a0002 | c0004 | t0008 | g0213 | AFR | ESN | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG03540 | hp1 | a0003 | c0002 | t0075 | g0160 | AFR | GWD | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG03540 | hp2 | a0002 | c0003 | t0036 | g0022 | AFR | GWD | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG03579 | hp1 | a0003 | c0002 | t0019 | g0165 | AFR | MSL | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG03579 | hp2 | a0001 | c0001 | t0011 | g0012 | AFR | MSL | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG03654 | hp1 | a0004 | c0006 | t0025 | g0166 | SAS | PJL | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG03654 | hp2 | a0005 | c0007 | t0006 | g0131 | SAS | PJL | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG03704 | hp1 | a0001 | c0008 | t0015 | g0076 | SAS | PJL | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG03704 | hp2 | a0002 | c0003 | t0004 | g0222 | SAS | PJL | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG03710 | hp1 | a0001 | c0001 | t0067 | g0112 | SAS | PJL | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG03710 | hp2 | a0001 | c0001 | t0065 | g0115 | SAS | PJL | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG03831 | hp1 | a0001 | c0001 | t0058 | g0110 | SAS | BEB | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG03831 | hp2 | a0001 | c0001 | t0033 | g0138 | SAS | BEB | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0096 | SAS | BEB | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG03834 | hp2 | a0010 | c0013 | t0099 | g0183 | SAS | BEB | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG04115 | hp1 | a0001 | c0001 | t0070 | g0090 | SAS | STU | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG04115 | hp2 | a0003 | c0002 | t0106 | g0162 | SAS | STU | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG04184 | hp1 | a0006 | c0005 | t0041 | g0243 | SAS | BEB | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG04184 | hp2 | a0001 | c0001 | t0015 | g0065 | SAS | BEB | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG04199 | hp1 | a0002 | c0004 | t0009 | g0042 | SAS | STU | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG04199 | hp2 | a0005 | c0007 | t0053 | g0155 | SAS | STU | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0099 | SAS | STU | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG04204 | hp2 | a0002 | c0003 | t0004 | g0223 | SAS | STU | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG04228 | hp1 | a0001 | c0001 | t0069 | g0129 | SAS | STU | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG04228 | hp2 | a0001 | c0008 | t0073 | g0078 | SAS | STU | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| NA18522 | hp1 | a0002 | c0003 | t0094 | g0019 | AFR | YRI | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| NA18522 | hp2 | a0007 | c0009 | t0022 | g0032 | AFR | YRI | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| NA18906 | hp1 | a0002 | c0004 | t0014 | g0018 | AFR | YRI | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| NA18906 | hp2 | a0007 | c0009 | t0022 | g0005 | AFR | YRI | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| NA18939 | hp2 | a0003 | c0002 | t0001 | g0189 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| NA18942 | hp1 | a0002 | c0003 | t0005 | g0196 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| NA18942 | hp2 | a0001 | c0001 | t0003 | g0051 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| NA18944 | hp2 | a0002 | c0004 | t0038 | g0020 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| NA18948 | hp1 | a0002 | c0003 | t0013 | g0239 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| NA18948 | hp2 | a0001 | c0001 | t0003 | g0087 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| NA18952 | hp1 | a0002 | c0003 | t0013 | g0253 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| NA18952 | hp2 | a0001 | c0001 | t0017 | g0052 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| NA18954 | hp1 | a0001 | c0001 | t0032 | g0081 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| NA18954 | hp2 | a0002 | c0003 | t0002 | g0237 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| NA18957 | hp1 | a0003 | c0002 | t0001 | g0021 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| NA18959 | hp1 | a0002 | c0004 | t0081 | g0227 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| NA18962 | hp1 | a0001 | c0001 | t0010 | g0007 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| NA18962 | hp2 | a0001 | c0001 | t0003 | g0139 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| NA18964 | hp1 | a0001 | c0001 | t0003 | g0121 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| NA18964 | hp2 | a0002 | c0003 | t0005 | g0233 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| NA18969 | hp2 | a0002 | c0004 | t0038 | g0020 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| NA18970 | hp1 | a0001 | c0001 | t0055 | g0136 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| NA18970 | hp2 | a0001 | c0001 | t0016 | g0003 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| NA18972 | hp1 | a0001 | c0001 | t0063 | g0066 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| NA18972 | hp2 | a0002 | c0004 | t0037 | g0228 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| NA18974 | hp1 | a0002 | c0003 | t0013 | g0004 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| NA18974 | hp2 | a0003 | c0002 | t0001 | g0021 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| NA18981 | hp1 | a0002 | c0003 | t0013 | g0236 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| NA18981 | hp2 | a0001 | c0001 | t0003 | g0154 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| NA18982 | hp1 | a0001 | c0001 | t0034 | g0093 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| NA18982 | hp2 | a0001 | c0001 | t0003 | g0059 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| NA18983 | hp2 | a0001 | c0001 | t0003 | g0071 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| NA18986 | hp1 | a0001 | c0001 | t0060 | g0049 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| NA18986 | hp2 | a0001 | c0001 | t0003 | g0058 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| NA18987 | hp1 | a0018 | c0027 | t0005 | g0232 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| NA18987 | hp2 | a0001 | c0001 | t0003 | g0107 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| NA18998 | hp1 | a0001 | c0001 | t0007 | g0095 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| NA18998 | hp2 | a0002 | c0003 | t0013 | g0004 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| NA19000 | hp1 | a0001 | c0001 | t0054 | g0135 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| NA19000 | hp2 | a0003 | c0002 | t0064 | g0146 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| NA19003 | hp1 | a0003 | c0002 | t0089 | g0191 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| NA19005 | hp1 | a0002 | c0003 | t0005 | g0249 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| NA19005 | hp2 | a0001 | c0001 | t0068 | g0101 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| NA19007 | hp1 | a0001 | c0001 | t0048 | g0086 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| NA19007 | hp2 | a0003 | c0002 | t0001 | g0214 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| NA19009 | hp1 | a0001 | c0001 | t0010 | g0120 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| NA19009 | hp2 | a0002 | c0003 | t0005 | g0229 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| NA19011 | hp1 | a0003 | c0002 | t0005 | g0224 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| NA19011 | hp2 | a0001 | c0001 | t0032 | g0007 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| NA19012 | hp1 | a0003 | c0002 | t0076 | g0238 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| NA19012 | hp2 | a0001 | c0001 | t0003 | g0137 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| NA19030 | hp1 | a0003 | c0002 | t0004 | g0172 | AFR | LWK | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| NA19030 | hp2 | a0003 | c0011 | t0091 | g0001 | AFR | LWK | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| NA19043 | hp1 | a0002 | c0003 | t0002 | g0210 | AFR | LWK | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| NA19043 | hp2 | a0002 | c0003 | t0098 | g0171 | AFR | LWK | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| NA19062 | hp1 | a0002 | c0003 | t0013 | g0004 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| NA19062 | hp2 | a0001 | c0001 | t0010 | g0082 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| NA19066 | hp1 | a0002 | c0003 | t0005 | g0230 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| NA19066 | hp2 | a0001 | c0001 | t0010 | g0102 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| NA19070 | hp2 | a0001 | c0001 | t0056 | g0092 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| NA19085 | hp1 | a0001 | c0001 | t0016 | g0003 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| NA19085 | hp2 | a0002 | c0004 | t0009 | g0190 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| NA19086 | hp1 | a0002 | c0003 | t0103 | g0194 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| NA19089 | hp1 | a0001 | c0001 | t0003 | g0075 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| NA19089 | hp2 | a0003 | c0002 | t0010 | g0205 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| NA19090 | hp1 | a0001 | c0001 | t0010 | g0068 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| NA19091 | hp1 | a0001 | c0001 | t0016 | g0003 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| NA19240 | hp1 | a0001 | c0001 | t0031 | g0056 | AFR | YRI | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| NA19240 | hp2 | a0003 | c0002 | t0026 | g0041 | AFR | YRI | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| NA20129 | hp1 | a0003 | c0014 | t0043 | g0217 | AFR | ASW | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| NA20129 | hp2 | a0006 | c0005 | t0002 | g0245 | AFR | ASW | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| NA20752 | hp1 | a0003 | c0002 | t0102 | g0207 | EUR | TSI | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| NA20752 | hp2 | a0002 | c0003 | t0105 | g0173 | EUR | TSI | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| NA20905 | hp1 | a0002 | c0024 | t0108 | g0250 | SAS | GIH | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| NA20905 | hp2 | a0002 | c0003 | t0004 | g0199 | SAS | GIH | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG01123 | hp1 | a0002 | c0003 | t0002 | g0045 | AMR | CLM | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG01123 | hp2 | a0001 | c0001 | t0007 | g0142 | AMR | CLM | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG02109 | hp1 | a0001 | c0008 | t0029 | g0152 | AFR | ACB | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG02109 | hp2 | a0009 | c0012 | t0023 | g0027 | AFR | ACB | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG02486 | hp1 | a0007 | c0009 | t0022 | g0005 | AFR | ACB | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG02486 | hp2 | a0001 | c0001 | t0031 | g0067 | AFR | ACB | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG02559 | hp1 | a0002 | c0003 | t0036 | g0022 | AFR | ACB | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG02559 | hp2 | a0012 | c0031 | t0045 | g0025 | AFR | ACB | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG03471 | hp1 | a0006 | c0005 | t0004 | g0244 | AFR | MSL | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG03471 | hp2 | a0003 | c0002 | t0021 | g0151 | AFR | MSL | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG06807 | hp1 | a0008 | c0015 | t0012 | g0017 | AFR | USA | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| HG06807 | hp2 | a0003 | c0011 | t0012 | g0061 | AFR | USA | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| NA18955 | hp1 | a0002 | c0003 | t0013 | g0240 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| NA18955 | hp2 | a0001 | c0001 | t0017 | g0084 | EAS | JPT | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| NA20300 | hp1 | a0008 | c0015 | t0012 | g0017 | AFR | USA | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| NA20300 | hp2 | a0009 | c0012 | t0023 | g0026 | AFR | USA | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| NA21309 | hp1 | a0007 | c0020 | t0061 | g0029 | AFR | LWK | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| NA21309 | hp2 | a0002 | c0004 | t0008 | g0180 | AFR | LWK | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| homoSapiens | chm13v2 | a0004 | c0006 | t0086 | g0285 | REF | REF | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| homoSapiens | grch38p0 | a0004 | c0006 | t0025 | g0273 | REF | REF | ABCG8_chr2_43833971_43887988 | ABCG8 | chr2 | 43833971 | 43887988 |
| view | chr:pos | ref | alt | # # of ahapid:amio-acid(protein) level
|
ahapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:43839108 | G | C | 2 | a0006a0010 | 15 | HG00438.hp1 HG00741.hp2 HG01943.hp1 others(12): Show |
missense_variant | MODERATE | c.55G>C | p.Asp19His | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/13 | 138/7180 | 55/2022 | 19/673 | chr2 | 43839108 | |||
| chr2:43844537 | A | G | 2 | a0009a0012 | 5 | HG02109.hp2 HG02559.hp2 HG03098.hp1 others(2): Show |
missense_variant | MODERATE | c.94A>G | p.Ser32Gly | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 2/13 | 177/7180 | 94/2022 | 32/673 | chr2 | 43844537 | |||
| chr2:43844597 | C | G | 2 | a0008a0017 | 6 | HG02896.hp2 HG02897.hp1 HG03195.hp2 others(3): Show |
missense_variant | MODERATE | c.154C>G | p.Leu52Val | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 2/13 | 237/7180 | 154/2022 | 52/673 | chr2 | 43844597 | |||
| chr2:43844604 | A | G | 4 | a0001a0005a0013others(1): Show | 125 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(122): Show |
missense_variant | MODERATE | c.161A>G | p.Tyr54Cys | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 2/13 | 244/7180 | 161/2022 | 54/673 | chr2 | 43844604 | |||
| chr2:43846228 | G | A | 3 | a0007a0009a0012 | 12 | HG01346.hp2 HG02109.hp2 HG02486.hp1 others(9): Show |
missense_variant | MODERATE | c.239G>A | p.Cys80Tyr | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/13 | 322/7180 | 239/2022 | 80/673 | chr2 | 43846228 | |||
| chr2:43852420 | G | A | 1 | a0007 | 7 | HG01346.hp2 HG02486.hp1 HG02630.hp1 others(4): Show |
missense_variant | MODERATE | c.628G>A | p.Val210Met | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 5/13 | 711/7180 | 628/2022 | 210/673 | chr2 | 43852420 | |||
| chr2:43852601 | A | G | 1 | a0015 | 1 | HG02717.hp2 | missense_variant&splice_region_variant | MODERATE | c.697A>G | p.Ile233Val | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/13 | 780/7180 | 697/2022 | 233/673 | chr2 | 43852601 | |||
| chr2:43852626 | C | T | 1 | a0016 | 1 | HG03017.hp2 | missense_variant | MODERATE | c.722C>T | p.Ser241Phe | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/13 | 805/7180 | 722/2022 | 241/673 | chr2 | 43852626 | |||
| chr2:43852664 | A | G | 1 | a0018 | 1 | NA18987.hp1 | missense_variant | MODERATE | c.760A>G | p.Thr254Ala | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/13 | 843/7180 | 760/2022 | 254/673 | chr2 | 43852664 | |||
| chr2:43871979 | A | T | 1 | a0013 | 1 | HG02602.hp2 | missense_variant | MODERATE | c.968A>T | p.Asp323Val | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 7/13 | 1051/7180 | 968/2022 | 323/673 | chr2 | 43871979 | |||
| chr2:43872294 | C | A | 5 | a0002a0008a0010others(2): Show | 88 | HG00280.hp2 HG00323.hp1 HG00621.hp1 others(85): Show |
missense_variant | MODERATE | c.1199C>A | p.Thr400Lys | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 8/13 | 1282/7180 | 1199/2022 | 400/673 | chr2 | 43872294 | |||
| chr2:43877786 | T | C | 15 | a0001a0002a0003others(12): Show | 293 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(290): Show |
missense_variant | MODERATE | c.1895T>C | p.Val632Ala | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 1978/7180 | 1895/2022 | 632/673 | chr2 | 43877786 | |||
| chr2:43877854 | A | G | 2 | a0012a0014 | 2 | HG02559.hp2 HG02647.hp1 |
missense_variant | MODERATE | c.1963A>G | p.Met655Val | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 2046/7180 | 1963/2022 | 655/673 | chr2 | 43877854 |
| 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_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:43839104 | C | A | 4 | a0008c0015a0008c0016a0008c0018others(1): Show | 6 | HG02896.hp2 HG02897.hp1 HG03195.hp2 others(3): Show |
synonymous_variant | LOW | c.51C>A | p.Pro17Pro | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/13 | 134/7180 | 51/2022 | 17/673 | chr2 | 43839104 | |||
| chr2:43851714 | G | A | 4 | a0003c0021a0003c0022a0006c0005others(1): Show | 17 | HG00438.hp1 HG00741.hp2 HG01943.hp1 others(14): Show |
synonymous_variant | LOW | c.453G>A | p.Val151Val | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 4/13 | 536/7180 | 453/2022 | 151/673 | chr2 | 43851714 | |||
| chr2:43852467 | G | A | 1 | a0003c0010 | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
synonymous_variant | LOW | c.675G>A | p.Val225Val | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 5/13 | 758/7180 | 675/2022 | 225/673 | chr2 | 43852467 | |||
| chr2:43852774 | C | T | 1 | a0002c0026 | 1 | HG02083.hp1 | synonymous_variant | LOW | c.870C>T | p.Thr290Thr | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/13 | 953/7180 | 870/2022 | 290/673 | chr2 | 43852774 | |||
| chr2:43873940 | C | T | 1 | a0003c0011 | 4 | HG02647.hp2 HG03130.hp1 HG06807.hp2 others(1): Show |
synonymous_variant | LOW | c.1365C>T | p.Ile455Ile | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 9/13 | 1448/7180 | 1365/2022 | 455/673 | chr2 | 43873940 | |||
| chr2:43873961 | C | T | 1 | a0016c0030 | 1 | HG03017.hp2 | synonymous_variant | LOW | c.1386C>T | p.Asn462Asn | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 9/13 | 1469/7180 | 1386/2022 | 462/673 | chr2 | 43873961 | |||
| chr2:43875226 | A | G | 1 | a0002c0024 | 1 | NA20905.hp1 | synonymous_variant | LOW | c.1569A>G | p.Pro523Pro | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 11/13 | 1652/7180 | 1569/2022 | 523/673 | chr2 | 43875226 | |||
| chr2:43875313 | G | A | 1 | a0012c0031 | 1 | HG02559.hp2 | synonymous_variant | LOW | c.1656G>A | p.Leu552Leu | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 11/13 | 1739/7180 | 1656/2022 | 552/673 | chr2 | 43875313 | |||
| chr2:43875352 | C | T | 8 | a0001c0008a0002c0004a0003c0014others(5): Show | 45 | HG00323.hp1 HG00642.hp1 HG00738.hp2 others(42): Show |
synonymous_variant | LOW | c.1695C>T | p.Ala565Ala | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 11/13 | 1778/7180 | 1695/2022 | 565/673 | chr2 | 43875352 | |||
| chr2:43875373 | C | T | 1 | a0008c0015 | 2 | HG06807.hp1 NA20300.hp1 |
synonymous_variant | LOW | c.1716C>T | p.Leu572Leu | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 11/13 | 1799/7180 | 1716/2022 | 572/673 | chr2 | 43875373 | |||
| chr2:43877586 | C | T | 1 | a0003c0017 | 2 | HG00642.hp2 HG01099.hp2 |
synonymous_variant | LOW | c.1782C>T | p.Ser594Ser | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 12/13 | 1865/7180 | 1782/2022 | 594/673 | chr2 | 43877586 |
| 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_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:43839035 | T | G | 59 | a0001c0001t0001a0001c0001t0003a0001c0001t0007others(56): Show | 158 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(155): Show |
5_prime_UTR_variant | MODIFIER | c.-19T>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/13 | 19 | chr2 | 43839035 | ||||||
| chr2:43839039 | A | C | 4 | a0003c0002t0018a0003c0002t0019a0003c0002t0075others(1): Show | 10 | HG01074.hp1 HG01099.hp1 HG01109.hp2 others(7): Show |
5_prime_UTR_variant | MODIFIER | c.-15A>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/13 | 15 | chr2 | 43839039 | ||||||
| chr2:43878065 | A | G | 1 | a0001c0008t0073 | 1 | HG04228.hp2 | 3_prime_UTR_variant | MODIFIER | c.*152A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 152 | chr2 | 43878065 | ||||||
| chr2:43878663 | C | T | 1 | a0009c0012t0072 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*750C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 750 | chr2 | 43878663 | ||||||
| chr2:43878728 | T | C | 1 | a0012c0031t0045 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*815T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 815 | chr2 | 43878728 | ||||||
| chr2:43878748 | T | C | 2 | a0002c0003t0036a0003c0002t0021 | 5 | HG02559.hp1 HG02622.hp1 HG02976.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*835T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 835 | chr2 | 43878748 | ||||||
| chr2:43878817 | C | G | 1 | a0001c0001t0071 | 1 | HG01934.hp2 | 3_prime_UTR_variant | MODIFIER | c.*904C>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 904 | chr2 | 43878817 | ||||||
| chr2:43878916 | G | A | 2 | a0007c0009t0022a0007c0009t0028 | 5 | HG02486.hp1 HG02630.hp1 HG02896.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1003G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 1003 | chr2 | 43878916 | ||||||
| chr2:43878918 | C | T | 83 | a0001c0001t0001a0001c0001t0007a0001c0001t0010others(80): Show | 197 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(194): Show |
3_prime_UTR_variant | MODIFIER | c.*1005C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 1005 | chr2 | 43878918 | ||||||
| chr2:43878919 | G | A | 1 | a0014c0025t0074 | 1 | HG02647.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1006G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 1006 | chr2 | 43878919 | ||||||
| chr2:43878943 | C | T | 1 | a0003c0010t0110 | 1 | HG02895.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1030C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 1030 | chr2 | 43878943 | ||||||
| chr2:43879038 | T | C | 1 | a0001c0001t0058 | 1 | HG03831.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1125T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 1125 | chr2 | 43879038 | ||||||
| chr2:43879060 | T | C | 1 | a0003c0002t0089 | 1 | NA19003.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1147T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 1147 | chr2 | 43879060 | ||||||
| chr2:43879076 | T | C | 1 | a0002c0003t0090 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1163T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 1163 | chr2 | 43879076 | ||||||
| chr2:43879311 | C | A | 6 | a0001c0001t0059a0002c0003t0012a0003c0002t0092others(3): Show | 10 | HG02647.hp2 HG02965.hp1 HG02976.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1398C>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 1398 | chr2 | 43879311 | ||||||
| chr2:43879402 | A | T | 15 | a0001c0001t0003a0001c0001t0016a0001c0001t0030others(12): Show | 47 | HG00438.hp2 HG00597.hp1 HG00597.hp2 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*1489A>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 1489 | chr2 | 43879402 | ||||||
| chr2:43879414 | T | G | 2 | a0003c0002t0042a0003c0002t0093 | 3 | HG01884.hp2 HG02809.hp2 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1501T>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 1501 | chr2 | 43879414 | ||||||
| chr2:43879462 | G | C | 4 | a0002c0003t0094a0003c0002t0093a0007c0009t0022others(1): Show | 7 | HG01884.hp2 HG02486.hp1 HG02630.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1549G>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 1549 | chr2 | 43879462 | ||||||
| chr2:43879518 | G | A | 1 | a0003c0002t0095 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1605G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 1605 | chr2 | 43879518 | ||||||
| chr2:43879568 | A | G | 1 | a0001c0001t0057 | 1 | HG02074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1655A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 1655 | chr2 | 43879568 | ||||||
| chr2:43879579 | T | A | 1 | a0002c0003t0096 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1666T>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 1666 | chr2 | 43879579 | ||||||
| chr2:43879759 | C | G | 3 | a0001c0001t0070a0002c0003t0020a0003c0010t0020 | 5 | HG00280.hp2 HG01192.hp1 HG03490.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1846C>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 1846 | chr2 | 43879759 | ||||||
| chr2:43879801 | T | C | 1 | a0002c0003t0097 | 1 | HG02055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1888T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 1888 | chr2 | 43879801 | ||||||
| chr2:43879815 | C | G | 2 | a0012c0031t0045a0014c0025t0074 | 2 | HG02559.hp2 HG02647.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1902C>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 1902 | chr2 | 43879815 | ||||||
| chr2:43879963 | C | G | 1 | a0006c0005t0088 | 1 | HG01978.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2050C>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 2050 | chr2 | 43879963 | ||||||
| chr2:43880029 | T | G | 1 | a0001c0001t0060 | 1 | NA18986.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2116T>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 2116 | chr2 | 43880029 | ||||||
| chr2:43880085 | C | A | 1 | a0001c0001t0016 | 4 | HG00438.hp2 NA18970.hp2 NA19085.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2172C>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 2172 | chr2 | 43880085 | ||||||
| chr2:43880091 | C | T | 1 | a0003c0010t0110 | 1 | HG02895.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2178C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 2178 | chr2 | 43880091 | ||||||
| chr2:43880121 | C | A | 1 | a0016c0030t0046 | 1 | HG03017.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2208C>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 2208 | chr2 | 43880121 | ||||||
| chr2:43880156 | T | C | 3 | a0001c0001t0070a0002c0003t0020a0003c0010t0020 | 5 | HG00280.hp2 HG01192.hp1 HG03490.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2243T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 2243 | chr2 | 43880156 | ||||||
| chr2:43880166 | A | AT | 4 | a0001c0001t0011a0001c0001t0035a0003c0002t0075others(1): Show | 11 | HG01106.hp2 HG02451.hp1 HG02572.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2259dupT | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 2260 | INFO_REALIGN_3_PRIME | chr2 | 43880166 | |||||
| chr2:43880172 | TG | T | 14 | a0001c0001t0007a0001c0001t0016a0001c0001t0031others(11): Show | 41 | HG00099.hp2 HG00438.hp2 HG00642.hp2 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*2260delG | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 2260 | chr2 | 43880172 | ||||||
| chr2:43880173 | G | GT | 39 | a0001c0001t0001a0001c0001t0010a0001c0001t0017others(36): Show | 83 | HG00099.hp1 HG00438.hp1 HG00597.hp1 others(80): Show |
3_prime_UTR_variant | MODIFIER | c.*2264dupT | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 2265 | INFO_REALIGN_3_PRIME | chr2 | 43880173 | |||||
| chr2:43880173 | G | GTT | 12 | a0001c0001t0001a0001c0001t0032a0001c0001t0062others(9): Show | 27 | HG00280.hp2 HG00558.hp2 HG00639.hp1 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*2263_*2264dupTT | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 2265 | INFO_REALIGN_3_PRIME | chr2 | 43880173 | |||||
| chr2:43880173 | G | T | 10 | a0001c0001t0007a0001c0001t0011a0001c0001t0035others(7): Show | 22 | HG00558.hp1 HG00621.hp2 HG00639.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*2260G>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 2260 | chr2 | 43880173 | ||||||
| chr2:43880177 | TG | T | 32 | a0001c0001t0003a0001c0001t0048a0001c0001t0055others(29): Show | 68 | HG00597.hp2 HG00621.hp1 HG00673.hp2 others(65): Show |
3_prime_UTR_variant | MODIFIER | c.*2265delG | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 2265 | chr2 | 43880177 | ||||||
| chr2:43880178 | G | T | 102 | a0001c0001t0001a0001c0001t0003a0001c0001t0007others(99): Show | 243 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(240): Show |
3_prime_UTR_variant | MODIFIER | c.*2265G>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 2265 | chr2 | 43880178 | ||||||
| chr2:43880180 | T | G | 6 | a0001c0001t0059a0002c0003t0012a0003c0002t0092others(3): Show | 10 | HG02647.hp2 HG02965.hp1 HG02976.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2267T>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 2267 | chr2 | 43880180 | ||||||
| chr2:43880183 | T | G | 1 | a0002c0003t0098 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2270T>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 2270 | chr2 | 43880183 | ||||||
| chr2:43880214 | C | T | 1 | a0012c0031t0045 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2301C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 2301 | chr2 | 43880214 | ||||||
| chr2:43880218 | G | T | 1 | a0002c0003t0096 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2305G>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 2305 | chr2 | 43880218 | ||||||
| chr2:43880332 | CCTGG | C | 22 | a0001c0001t0007a0001c0001t0031a0002c0003t0002others(19): Show | 57 | HG00099.hp2 HG00558.hp1 HG00621.hp2 others(54): Show |
3_prime_UTR_variant | MODIFIER | c.*2422_*2425delGGCT | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 2422 | INFO_REALIGN_3_PRIME | chr2 | 43880332 | |||||
| chr2:43880336 | G | C | 2 | a0002c0003t0036a0003c0002t0021 | 5 | HG02559.hp1 HG02622.hp1 HG02976.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2423G>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 2423 | chr2 | 43880336 | ||||||
| chr2:43880562 | T | C | 53 | a0001c0001t0001a0001c0001t0010a0001c0001t0011others(50): Show | 127 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(124): Show |
3_prime_UTR_variant | MODIFIER | c.*2649T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 2649 | chr2 | 43880562 | ||||||
| chr2:43880596 | T | A | 125 | a0001c0001t0001a0001c0001t0003a0001c0001t0007others(122): Show | 293 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(290): Show |
3_prime_UTR_variant | MODIFIER | c.*2683T>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 2683 | chr2 | 43880596 | ||||||
| chr2:43880603 | G | T | 39 | a0001c0001t0007a0001c0001t0031a0001c0001t0059others(36): Show | 84 | HG00099.hp2 HG00558.hp1 HG00621.hp2 others(81): Show |
3_prime_UTR_variant | MODIFIER | c.*2690G>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 2690 | chr2 | 43880603 | ||||||
| chr2:43880630 | T | C | 1 | a0002c0003t0101 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2717T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 2717 | chr2 | 43880630 | ||||||
| chr2:43880649 | A | AGT | 40 | a0001c0001t0001a0001c0001t0010a0001c0001t0011others(37): Show | 104 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(101): Show |
3_prime_UTR_variant | MODIFIER | c.*2750_*2751dupTG | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 2752 | INFO_REALIGN_3_PRIME | chr2 | 43880649 | |||||
| chr2:43880649 | A | AGTGT | 3 | a0001c0001t0068a0002c0003t0013a0002c0003t0096 | 9 | HG02572.hp2 NA18948.hp1 NA18952.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2748_*2751dupTGTG | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 2752 | INFO_REALIGN_3_PRIME | chr2 | 43880649 | |||||
| chr2:43880649 | A | T | 1 | a0001c0001t0069 | 1 | HG04228.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2736A>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 2736 | chr2 | 43880649 | ||||||
| chr2:43880663 | T | C | 24 | a0001c0001t0007a0001c0001t0031a0002c0003t0002others(21): Show | 59 | HG00099.hp2 HG00558.hp1 HG00621.hp2 others(56): Show |
3_prime_UTR_variant | MODIFIER | c.*2750T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 2750 | chr2 | 43880663 | ||||||
| chr2:43880663 | T | TGC | 7 | a0001c0001t0056a0001c0008t0050a0001c0008t0051others(4): Show | 7 | HG01255.hp2 HG01884.hp1 HG02055.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2765_*2766dupGC | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 2767 | INFO_REALIGN_3_PRIME | chr2 | 43880663 | |||||
| chr2:43880665 | C | T | 63 | a0001c0001t0001a0001c0001t0007a0001c0001t0010others(60): Show | 157 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(154): Show |
3_prime_UTR_variant | MODIFIER | c.*2752C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 2752 | chr2 | 43880665 | ||||||
| chr2:43880667 | C | T | 2 | a0001c0001t0035a0014c0025t0074 | 3 | HG02647.hp1 HG02895.hp1 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2754C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 2754 | chr2 | 43880667 | ||||||
| chr2:43880670 | G | A | 4 | a0001c0001t0010a0001c0001t0063a0002c0003t0103others(1): Show | 9 | HG02015.hp2 NA18962.hp1 NA18972.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2757G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 2757 | chr2 | 43880670 | ||||||
| chr2:43880675 | C | T | 31 | a0001c0001t0007a0001c0001t0031a0002c0003t0002others(28): Show | 72 | HG00099.hp2 HG00558.hp1 HG00621.hp2 others(69): Show |
3_prime_UTR_variant | MODIFIER | c.*2762C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 2762 | chr2 | 43880675 | ||||||
| chr2:43880677 | C | T | 1 | a0003c0010t0110 | 1 | HG02895.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2764C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 2764 | chr2 | 43880677 | ||||||
| chr2:43880686 | A | G | 8 | a0001c0001t0070a0002c0003t0020a0002c0003t0036others(5): Show | 13 | HG00280.hp2 HG01192.hp1 HG02559.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*2773A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 2773 | chr2 | 43880686 | ||||||
| chr2:43880726 | C | T | 3 | a0001c0001t0070a0002c0003t0020a0003c0010t0020 | 5 | HG00280.hp2 HG01192.hp1 HG03490.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2813C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 2813 | chr2 | 43880726 | ||||||
| chr2:43880822 | C | T | 1 | a0007c0009t0028 | 2 | HG02630.hp1 HG02896.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2909C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 2909 | chr2 | 43880822 | ||||||
| chr2:43880962 | A | G | 1 | a0001c0001t0063 | 1 | NA18972.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3049A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 3049 | chr2 | 43880962 | ||||||
| chr2:43880982 | C | T | 1 | a0012c0031t0045 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3069C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 3069 | chr2 | 43880982 | ||||||
| chr2:43881194 | G | A | 6 | a0002c0003t0094a0003c0002t0093a0003c0002t0104others(3): Show | 9 | HG01884.hp2 HG02486.hp1 HG02630.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*3281G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 3281 | chr2 | 43881194 | ||||||
| chr2:43881243 | A | T | 1 | a0001c0001t0047 | 1 | HG02083.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3330A>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 3330 | chr2 | 43881243 | ||||||
| chr2:43881261 | A | T | 1 | a0001c0001t0058 | 1 | HG03831.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3348A>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 3348 | chr2 | 43881261 | ||||||
| chr2:43881438 | C | T | 1 | a0003c0002t0095 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3525C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 3525 | chr2 | 43881438 | ||||||
| chr2:43881521 | C | T | 1 | a0003c0002t0095 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3608C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 3608 | chr2 | 43881521 | ||||||
| chr2:43881525 | A | G | 1 | a0011c0023t0084 | 1 | HG01993.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3612A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 3612 | chr2 | 43881525 | ||||||
| chr2:43881669 | A | C | 2 | a0003c0002t0042a0012c0031t0045 | 3 | HG02559.hp2 HG02809.hp2 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3756A>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 3756 | chr2 | 43881669 | ||||||
| chr2:43881697 | T | G | 127 | a0001c0001t0001a0001c0001t0003a0001c0001t0007others(124): Show | 296 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(293): Show |
3_prime_UTR_variant | MODIFIER | c.*3784T>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 3784 | chr2 | 43881697 | ||||||
| chr2:43881707 | C | CA | 48 | a0001c0001t0007a0001c0001t0015a0001c0001t0017others(45): Show | 96 | HG00099.hp2 HG00438.hp1 HG00558.hp1 others(93): Show |
3_prime_UTR_variant | MODIFIER | c.*3812dupA | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 3813 | INFO_REALIGN_3_PRIME | chr2 | 43881707 | |||||
| chr2:43881707 | C | CAA | 8 | a0001c0001t0031a0002c0003t0094a0002c0004t0037others(5): Show | 15 | HG01175.hp2 HG01433.hp2 HG01884.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*3811_*3812dupAA | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 3813 | INFO_REALIGN_3_PRIME | chr2 | 43881707 | |||||
| chr2:43881726 | C | A | 50 | a0001c0001t0007a0001c0001t0017a0001c0001t0031others(47): Show | 100 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(97): Show |
3_prime_UTR_variant | MODIFIER | c.*3813C>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 3813 | chr2 | 43881726 | ||||||
| chr2:43881898 | C | T | 1 | a0003c0010t0110 | 1 | HG02895.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3985C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 3985 | chr2 | 43881898 | ||||||
| chr2:43881953 | G | A | 3 | a0002c0003t0036a0002c0003t0098a0003c0002t0021 | 6 | HG02559.hp1 HG02622.hp1 HG02976.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4040G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 4040 | chr2 | 43881953 | ||||||
| chr2:43881965 | T | A | 1 | a0003c0010t0110 | 1 | HG02895.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4052T>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 4052 | chr2 | 43881965 | ||||||
| chr2:43882019 | G | C | 67 | a0001c0001t0001a0001c0001t0003a0001c0001t0010others(64): Show | 169 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(166): Show |
3_prime_UTR_variant | MODIFIER | c.*4106G>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 4106 | chr2 | 43882019 | ||||||
| chr2:43882069 | C | T | 1 | a0014c0025t0074 | 1 | HG02647.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4156C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 4156 | chr2 | 43882069 | ||||||
| chr2:43882142 | A | G | 67 | a0001c0001t0001a0001c0001t0003a0001c0001t0010others(64): Show | 173 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(170): Show |
3_prime_UTR_variant | MODIFIER | c.*4229A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 4229 | chr2 | 43882142 | ||||||
| chr2:43882368 | C | A | 42 | a0001c0001t0001a0001c0001t0010a0001c0001t0011others(39): Show | 109 | HG00099.hp1 HG00438.hp1 HG00558.hp2 others(106): Show |
3_prime_UTR_variant | MODIFIER | c.*4455C>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 4455 | chr2 | 43882368 | ||||||
| chr2:43882405 | C | G | 1 | a0001c0001t0054 | 1 | NA19000.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4492C>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 4492 | chr2 | 43882405 | ||||||
| chr2:43882468 | G | A | 1 | a0003c0002t0092 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4555G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 4555 | chr2 | 43882468 | ||||||
| chr2:43882485 | T | C | 8 | a0001c0001t0015a0001c0008t0015a0001c0008t0073others(5): Show | 19 | HG01069.hp2 HG01192.hp2 HG01256.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*4572T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 4572 | chr2 | 43882485 | ||||||
| chr2:43882611 | C | A | 1 | a0003c0010t0110 | 1 | HG02895.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4698C>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 4698 | chr2 | 43882611 | ||||||
| chr2:43882641 | G | A | 1 | a0001c0001t0065 | 1 | HG03710.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4728G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 4728 | chr2 | 43882641 | ||||||
| chr2:43882731 | C | G | 1 | a0012c0031t0045 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4818C>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 4818 | chr2 | 43882731 | ||||||
| chr2:43882863 | A | G | 1 | a0003c0002t0106 | 1 | HG04115.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4950A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 4950 | chr2 | 43882863 | ||||||
| chr2:43882954 | G | A | 6 | a0001c0001t0059a0002c0003t0012a0003c0002t0092others(3): Show | 10 | HG02647.hp2 HG02965.hp1 HG02976.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*5041G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 5041 | chr2 | 43882954 | ||||||
| chr2:43882957 | C | A | 6 | a0001c0001t0059a0002c0003t0012a0003c0002t0092others(3): Show | 10 | HG02647.hp2 HG02965.hp1 HG02976.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*5044C>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 13/13 | 5044 | chr2 | 43882957 |
| 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_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:43839282 | C | G | 1 | a0015c0028t0043g0291 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.63+166C>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | chr2 | 43839282 | |||||||
| chr2:43839403 | C | CT | 9 | a0001c0008t0008g0274a0003c0002t0002g0275a0003c0002t0002g0282others(6): Show | 9 | HG00642.hp1 HG00733.hp2 HG01070.hp2 others(6): Show |
intron_variant | MODIFIER | c.63+328dupT | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 43839403 | ||||||
| chr2:43839403 | C | CTT | 7 | a0003c0002t0002g0283a0003c0002t0002g0284a0003c0002t0002g0287others(4): Show | 7 | HG00735.hp1 HG00741.hp1 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.63+327_63+328dupTT | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 43839403 | ||||||
| chr2:43839403 | CTT | C | 17 | a0002c0003t0002g0255a0002c0003t0004g0248a0002c0003t0005g0249others(14): Show | 17 | HG00280.hp2 HG01346.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.63+327_63+328delTT | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 43839403 | ||||||
| chr2:43839403 | CTTT | C | 29 | a0002c0003t0002g0231a0002c0003t0002g0234a0002c0003t0002g0237others(26): Show | 32 | HG00438.hp1 HG01261.hp1 HG01433.hp1 others(29): Show |
intron_variant | MODIFIER | c.63+326_63+328delTT others(1): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 43839403 | ||||||
| chr2:43839403 | CTTTT | C | 38 | a0002c0003t0002g0019a0002c0003t0002g0197a0002c0003t0002g0200others(35): Show | 41 | HG00738.hp1 HG01070.hp1 HG01106.hp1 others(38): Show |
intron_variant | MODIFIER | c.63+325_63+328delTT others(2): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 43839403 | ||||||
| chr2:43839403 | CTTTTT | C | 15 | a0002c0003t0012g0177a0002c0003t0098g0171a0002c0003t0101g0178others(12): Show | 16 | HG00639.hp2 HG00738.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.63+324_63+328delTT others(3): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 43839403 | ||||||
| chr2:43839403 | CTTTTTTT others(3): Show |
C | 1 | a0002c0003t0039g0170 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.63+319_63+328delTT others(8): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 43839403 | ||||||
| chr2:43839403 | CTTTTTTT others(4): Show |
C | 3 | a0002c0003t0041g0169a0010c0013t0002g0167a0010c0013t0005g0168 | 3 | HG00621.hp1 HG01943.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.63+318_63+328delTT others(9): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 43839403 | ||||||
| chr2:43839403 | CTTTTTTT others(7): Show |
C | 3 | a0003c0002t0019g0165a0003c0002t0026g0164a0004c0006t0025g0166 | 3 | HG01433.hp2 HG03579.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.63+315_63+328delTT others(12): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 43839403 | ||||||
| chr2:43839403 | CTTTTTTT others(8): Show |
C | 18 | a0001c0001t0003g0153a0001c0001t0003g0154a0001c0008t0029g0152others(15): Show | 21 | HG00642.hp2 HG01074.hp1 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.63+314_63+328delTT others(13): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 43839403 | ||||||
| chr2:43839403 | CTTTTTTT others(9): Show |
C | 100 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(97): Show | 108 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.63+313_63+328delTT others(14): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 43839403 | ||||||
| chr2:43839403 | CTTTTTTT others(10): Show |
C | 19 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0003g0051others(16): Show | 20 | HG00558.hp2 HG00639.hp1 HG01169.hp1 others(17): Show |
intron_variant | MODIFIER | c.63+312_63+328delTT others(15): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 43839403 | ||||||
| chr2:43839403 | CTTTTTTT others(11): Show |
C | 2 | a0002c0003t0002g0044a0002c0003t0002g0045 | 2 | HG01123.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.63+311_63+328delTT others(16): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 43839403 | ||||||
| chr2:43839403 | CTTTTTTT others(13): Show |
C | 7 | a0002c0004t0009g0042a0003c0002t0026g0041a0003c0002t0092g0040others(4): Show | 7 | HG01168.hp2 HG01192.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.63+309_63+328delTT others(18): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 43839403 | ||||||
| chr2:43839403 | CTTTTTTT others(14): Show |
C | 2 | a0002c0003t0090g0035a0003c0010t0020g0036 | 2 | HG02809.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.63+308_63+328delTT others(19): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 43839403 | ||||||
| chr2:43839403 | CTTTTTTT others(17): Show |
C | 2 | a0007c0009t0028g0033a0007c0009t0028g0034 | 2 | HG02630.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.63+305_63+328delTT others(22): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 43839403 | ||||||
| chr2:43839403 | CTTTTTTT others(18): Show |
C | 10 | a0003c0021t0007g0030a0007c0009t0022g0005a0007c0009t0022g0032others(7): Show | 11 | HG01346.hp2 HG02109.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.63+304_63+328delTT others(23): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 43839403 | ||||||
| chr2:43839489 | T | C | 1 | a0003c0002t0019g0063 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.63+373T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | chr2 | 43839489 | |||||||
| chr2:43839642 | A | G | 1 | a0005c0007t0006g0148 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.63+526A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | chr2 | 43839642 | |||||||
| chr2:43839723 | G | A | 1 | a0017c0019t0109g0215 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.63+607G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | chr2 | 43839723 | |||||||
| chr2:43839737 | G | A | 295 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(292): Show | 315 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(312): Show |
intron_variant | MODIFIER | c.63+621G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | chr2 | 43839737 | |||||||
| chr2:43839860 | G | T | 2 | a0003c0002t0019g0163a0003c0002t0019g0165 | 2 | HG01109.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.63+744G>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | chr2 | 43839860 | |||||||
| chr2:43840030 | G | A | 120 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(117): Show | 129 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(126): Show |
intron_variant | MODIFIER | c.63+914G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | chr2 | 43840030 | |||||||
| chr2:43840081 | T | A | 2 | a0005c0007t0006g0006a0005c0007t0006g0064 | 3 | HG00280.hp1 HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.63+965T>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | chr2 | 43840081 | |||||||
| chr2:43840519 | C | T | 2 | a0001c0001t0007g0145a0001c0001t0010g0060 | 2 | HG00673.hp1 HG02015.hp2 |
intron_variant | MODIFIER | c.63+1403C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | chr2 | 43840519 | |||||||
| chr2:43840639 | C | G | 1 | a0003c0002t0001g0214 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.63+1523C>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | chr2 | 43840639 | |||||||
| chr2:43840680 | T | G | 158 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(155): Show | 171 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(168): Show |
intron_variant | MODIFIER | c.63+1564T>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | chr2 | 43840680 | |||||||
| chr2:43840711 | G | C | 1 | a0006c0005t0041g0243 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.63+1595G>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | chr2 | 43840711 | |||||||
| chr2:43840712 | C | T | 4 | a0001c0001t0007g0142a0001c0008t0015g0144a0001c0008t0051g0141others(1): Show | 4 | HG01123.hp2 HG01167.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.63+1596C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | chr2 | 43840712 | |||||||
| chr2:43840743 | C | T | 4 | a0001c0001t0001g0140a0001c0001t0003g0058a0001c0001t0003g0059others(1): Show | 4 | NA18962.hp2 NA18969.hp1 NA18982.hp2 others(1): Show |
intron_variant | MODIFIER | c.63+1627C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | chr2 | 43840743 | |||||||
| chr2:43840810 | A | C | 1 | a0006c0005t0004g0023 | 2 | HG02132.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.63+1694A>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | chr2 | 43840810 | |||||||
| chr2:43840857 | C | G | 2 | a0002c0004t0008g0271a0002c0004t0008g0272 | 2 | HG00323.hp1 HG01109.hp1 |
intron_variant | MODIFIER | c.63+1741C>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | chr2 | 43840857 | |||||||
| chr2:43841152 | C | T | 4 | a0001c0001t0007g0142a0001c0008t0015g0144a0001c0008t0051g0141others(1): Show | 4 | HG01123.hp2 HG01167.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.63+2036C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | chr2 | 43841152 | |||||||
| chr2:43841202 | C | G | 6 | a0003c0002t0026g0041a0003c0002t0092g0040a0003c0010t0020g0036others(3): Show | 6 | HG01192.hp1 HG02895.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.63+2086C>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | chr2 | 43841202 | |||||||
| chr2:43841220 | A | C | 1 | a0001c0001t0016g0003 | 3 | NA18970.hp2 NA19085.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.63+2104A>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | chr2 | 43841220 | |||||||
| chr2:43841260 | C | G | 1 | a0002c0003t0090g0035 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.63+2144C>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | chr2 | 43841260 | |||||||
| chr2:43841650 | G | A | 4 | a0003c0002t0021g0149a0003c0002t0021g0150a0003c0002t0021g0151others(1): Show | 5 | HG00642.hp2 HG01099.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.63+2534G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | chr2 | 43841650 | |||||||
| chr2:43841728 | T | G | 4 | a0003c0002t0021g0149a0003c0002t0021g0150a0003c0002t0021g0151others(1): Show | 5 | HG00642.hp2 HG01099.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.63+2612T>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | chr2 | 43841728 | |||||||
| chr2:43841755 | C | T | 1 | a0003c0002t0026g0041 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.63+2639C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | chr2 | 43841755 | |||||||
| chr2:43841837 | C | A | 6 | a0003c0002t0026g0041a0003c0002t0092g0040a0003c0010t0020g0036others(3): Show | 6 | HG01192.hp1 HG02895.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.64-2670C>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | chr2 | 43841837 | |||||||
| chr2:43841857 | C | A | 1 | a0002c0003t0090g0035 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.64-2650C>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | chr2 | 43841857 | |||||||
| chr2:43841873 | G | A | 3 | a0003c0011t0012g0001a0003c0011t0012g0061a0003c0011t0091g0001 | 4 | HG02647.hp2 HG03130.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.64-2634G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | chr2 | 43841873 | |||||||
| chr2:43841932 | T | C | 1 | a0009c0012t0072g0024 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.64-2575T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | chr2 | 43841932 | |||||||
| chr2:43841975 | GC | G | 4 | a0001c0001t0007g0142a0001c0008t0015g0144a0001c0008t0051g0141others(1): Show | 4 | HG01123.hp2 HG01167.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.64-2531delC | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | chr2 | 43841975 | |||||||
| chr2:43842013 | AT | A | 134 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(131): Show | 144 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(141): Show |
intron_variant | MODIFIER | c.64-2481delT | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 43842013 | ||||||
| chr2:43842075 | C | T | 1 | a0002c0004t0008g0213 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.64-2432C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | chr2 | 43842075 | |||||||
| chr2:43842199 | G | C | 1 | a0006c0005t0041g0243 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.64-2308G>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | chr2 | 43842199 | |||||||
| chr2:43842292 | C | T | 3 | a0001c0001t0003g0134a0001c0001t0054g0135a0001c0001t0055g0136 | 3 | HG00597.hp2 NA18970.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.64-2215C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | chr2 | 43842292 | |||||||
| chr2:43842304 | C | T | 1 | a0005c0007t0053g0155 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.64-2203C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | chr2 | 43842304 | |||||||
| chr2:43842378 | C | T | 138 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(135): Show | 149 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(146): Show |
intron_variant | MODIFIER | c.64-2129C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | chr2 | 43842378 | |||||||
| chr2:43842415 | C | G | 9 | a0003c0002t0018g0015a0003c0002t0018g0158a0003c0002t0018g0159others(6): Show | 10 | HG01074.hp1 HG01099.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.64-2092C>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | chr2 | 43842415 | |||||||
| chr2:43842563 | C | A | 117 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(114): Show | 125 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(122): Show |
intron_variant | MODIFIER | c.64-1944C>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | chr2 | 43842563 | |||||||
| chr2:43842601 | A | T | 1 | a0002c0003t0090g0035 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.64-1906A>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | chr2 | 43842601 | |||||||
| chr2:43842621 | G | A | 1 | a0002c0003t0098g0171 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.64-1886G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | chr2 | 43842621 | |||||||
| chr2:43842633 | G | A | 17 | a0003c0002t0004g0172a0003c0021t0007g0030a0003c0022t0014g0261others(14): Show | 18 | HG00438.hp1 HG00741.hp2 HG01943.hp1 others(15): Show |
intron_variant | MODIFIER | c.64-1874G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | chr2 | 43842633 | |||||||
| chr2:43842642 | A | T | 138 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(135): Show | 149 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(146): Show |
intron_variant | MODIFIER | c.64-1865A>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | chr2 | 43842642 | |||||||
| chr2:43842779 | A | AT | 138 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(135): Show | 149 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(146): Show |
intron_variant | MODIFIER | c.64-1721dupT | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 43842779 | ||||||
| chr2:43842891 | C | T | 4 | a0003c0002t0021g0149a0003c0002t0021g0150a0003c0002t0021g0151others(1): Show | 5 | HG00642.hp2 HG01099.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.64-1616C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | chr2 | 43842891 | |||||||
| chr2:43843073 | C | T | 3 | a0003c0011t0012g0001a0003c0011t0012g0061a0003c0011t0091g0001 | 4 | HG02647.hp2 HG03130.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.64-1434C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | chr2 | 43843073 | |||||||
| chr2:43843112 | T | C | 132 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(129): Show | 143 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(140): Show |
intron_variant | MODIFIER | c.64-1395T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | chr2 | 43843112 | |||||||
| chr2:43843158 | G | A | 2 | a0003c0002t0042g0016a0003c0002t0093g0161 | 3 | HG01884.hp2 HG02809.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.64-1349G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | chr2 | 43843158 | |||||||
| chr2:43843188 | A | AGCTTTT | 3 | a0001c0001t0007g0057a0001c0001t0031g0056a0001c0001t0059g0133 | 3 | HG03130.hp2 HG03195.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.64-1318_64-1313dup others(6): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 43843188 | ||||||
| chr2:43843255 | A | G | 117 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(114): Show | 125 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(122): Show |
intron_variant | MODIFIER | c.64-1252A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | chr2 | 43843255 | |||||||
| chr2:43843358 | T | A | 1 | a0012c0031t0045g0025 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.64-1149T>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | chr2 | 43843358 | |||||||
| chr2:43843391 | T | C | 1 | a0002c0004t0009g0262 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.64-1116T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | chr2 | 43843391 | |||||||
| chr2:43843414 | C | T | 11 | a0007c0009t0022g0005a0007c0009t0022g0032a0007c0009t0028g0033others(8): Show | 12 | HG01346.hp2 HG02109.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.64-1093C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | chr2 | 43843414 | |||||||
| chr2:43843500 | T | C | 174 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(171): Show | 188 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(185): Show |
intron_variant | MODIFIER | c.64-1007T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | chr2 | 43843500 | |||||||
| chr2:43843641 | G | A | 143 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(140): Show | 155 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(152): Show |
intron_variant | MODIFIER | c.64-866G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | chr2 | 43843641 | |||||||
| chr2:43843754 | A | T | 12 | a0002c0003t0002g0210a0002c0003t0012g0147a0002c0004t0008g0180others(9): Show | 12 | HG00738.hp2 HG01891.hp2 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.64-753A>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | chr2 | 43843754 | |||||||
| chr2:43843796 | A | G | 132 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(129): Show | 143 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(140): Show |
intron_variant | MODIFIER | c.64-711A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | chr2 | 43843796 | |||||||
| chr2:43843892 | C | T | 11 | a0007c0009t0022g0005a0007c0009t0022g0032a0007c0009t0028g0033others(8): Show | 12 | HG01346.hp2 HG02109.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.64-615C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | chr2 | 43843892 | |||||||
| chr2:43843915 | C | G | 1 | a0006c0005t0041g0243 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.64-592C>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | chr2 | 43843915 | |||||||
| chr2:43843930 | A | C | 1 | a0001c0001t0017g0132 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.64-577A>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | chr2 | 43843930 | |||||||
| chr2:43843947 | G | A | 1 | a0001c0001t0015g0065 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.64-560G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | chr2 | 43843947 | |||||||
| chr2:43844213 | T | A | 17 | a0003c0002t0018g0015a0003c0002t0018g0158a0003c0002t0018g0159others(14): Show | 19 | HG00642.hp2 HG01074.hp1 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.64-294T>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | chr2 | 43844213 | |||||||
| chr2:43844251 | G | C | 3 | a0002c0003t0002g0019a0002c0003t0094g0019a0002c0003t0096g0184 | 3 | HG00738.hp1 HG02572.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.64-256G>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | chr2 | 43844251 | |||||||
| chr2:43844313 | G | T | 2 | a0002c0003t0012g0177a0002c0003t0101g0178 | 2 | HG01884.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.64-194G>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | chr2 | 43844313 | |||||||
| chr2:43844394 | A | G | 5 | a0002c0003t0090g0035a0003c0002t0095g0242a0003c0002t0104g0216others(2): Show | 5 | HG02717.hp1 HG02717.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.64-113A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | chr2 | 43844394 | |||||||
| chr2:43844486 | C | A | 117 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(114): Show | 125 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(122): Show |
intron_variant | MODIFIER | c.64-21C>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | chr2 | 43844486 | |||||||
| chr2:43844500 | C | T | 143 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(140): Show | 155 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(152): Show |
splice_region_variant&intron_variant | LOW | c.64-7C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 1/12 | chr2 | 43844500 | |||||||
| chr2:43844621 | C | T | 3 | a0001c0001t0003g0130a0005c0007t0006g0131a0005c0007t0006g0148 | 3 | HG00733.hp1 HG01934.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.165+13C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 2/12 | chr2 | 43844621 | |||||||
| chr2:43844649 | G | A | 2 | a0003c0002t0002g0264a0004c0006t0024g0263 | 2 | HG00099.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.165+41G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 2/12 | chr2 | 43844649 | |||||||
| chr2:43844694 | A | C | 142 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(139): Show | 154 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(151): Show |
intron_variant | MODIFIER | c.165+86A>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 2/12 | chr2 | 43844694 | |||||||
| chr2:43844713 | G | C | 143 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(140): Show | 155 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(152): Show |
intron_variant | MODIFIER | c.165+105G>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 2/12 | chr2 | 43844713 | |||||||
| chr2:43844963 | G | A | 3 | a0002c0003t0012g0177a0002c0003t0101g0178a0002c0004t0008g0213 | 3 | HG01884.hp1 HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.165+355G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 2/12 | chr2 | 43844963 | |||||||
| chr2:43845006 | T | G | 117 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(114): Show | 125 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(122): Show |
intron_variant | MODIFIER | c.165+398T>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 2/12 | chr2 | 43845006 | |||||||
| chr2:43845080 | ATG | A | 14 | a0002c0003t0005g0229a0002c0004t0009g0190a0002c0004t0037g0228others(11): Show | 17 | HG01346.hp2 HG02486.hp1 HG02630.hp1 others(14): Show |
intron_variant | MODIFIER | c.165+490_165+491del others(2): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 43845080 | ||||||
| chr2:43845082 | G | A | 2 | a0001c0001t0017g0128a0001c0001t0069g0129 | 2 | HG02080.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.165+474G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 2/12 | chr2 | 43845082 | |||||||
| chr2:43845094 | G | GTA | 4 | a0009c0012t0023g0027a0009c0012t0023g0028a0009c0012t0072g0024others(1): Show | 4 | HG02109.hp2 HG02559.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.165+487_165+488ins others(2): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 43845094 | ||||||
| chr2:43845096 | G | A | 5 | a0009c0012t0023g0026a0009c0012t0023g0027a0009c0012t0023g0028others(2): Show | 5 | HG02109.hp2 HG02559.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.165+488G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 2/12 | chr2 | 43845096 | |||||||
| chr2:43845096 | G | GTA | 6 | a0001c0001t0001g0002a0001c0001t0001g0047a0001c0001t0001g0069others(3): Show | 8 | HG00558.hp2 HG02486.hp2 NA18939.hp1 others(5): Show |
intron_variant | MODIFIER | c.165+489_165+490ins others(2): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 43845096 | ||||||
| chr2:43845096 | G | GTATA | 3 | a0001c0001t0001g0070a0001c0001t0001g0072a0001c0001t0003g0071 | 3 | HG01081.hp2 HG02293.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.165+489_165+490ins others(4): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 43845096 | ||||||
| chr2:43845096 | GTGTA | G | 11 | a0002c0003t0004g0222a0002c0003t0004g0223a0002c0003t0107g0186others(8): Show | 11 | HG01256.hp1 HG01433.hp1 HG01496.hp2 others(8): Show |
intron_variant | MODIFIER | c.165+490_165+493del others(4): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 43845096 | ||||||
| chr2:43845096 | GTGTATA | G | 4 | a0003c0002t0021g0149a0003c0002t0021g0150a0003c0002t0021g0151others(1): Show | 5 | HG00642.hp2 HG01099.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.165+490_165+495del others(6): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 43845096 | ||||||
| chr2:43845098 | G | A | 136 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(133): Show | 147 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(144): Show |
intron_variant | MODIFIER | c.165+490G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 2/12 | chr2 | 43845098 | |||||||
| chr2:43845098 | G | GTA | 7 | a0003c0002t0026g0041a0003c0002t0026g0164a0003c0011t0012g0001others(4): Show | 9 | HG01433.hp2 HG02647.hp2 HG03130.hp1 others(6): Show |
intron_variant | MODIFIER | c.165+511_165+512dup others(2): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 43845098 | ||||||
| chr2:43845098 | GTA | G | 86 | a0002c0003t0002g0019a0002c0003t0002g0044a0002c0003t0002g0045others(83): Show | 90 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.165+511_165+512del others(2): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 43845098 | ||||||
| chr2:43845100 | A | G | 1 | a0002c0004t0009g0251 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.165+492A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 2/12 | chr2 | 43845100 | |||||||
| chr2:43845118 | AT | A | 4 | a0001c0008t0029g0152a0001c0008t0050g0073a0005c0007t0006g0006others(1): Show | 5 | HG00280.hp1 HG01069.hp1 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.165+511delT | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 2/12 | chr2 | 43845118 | |||||||
| chr2:43845119 | T | TATA | 10 | a0001c0001t0007g0057a0001c0001t0017g0128a0001c0001t0031g0056others(7): Show | 10 | HG00735.hp2 HG01081.hp1 HG01168.hp1 others(7): Show |
intron_variant | MODIFIER | c.165+512_165+513ins others(3): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 43845119 | ||||||
| chr2:43845121 | A | AT | 15 | a0001c0001t0003g0130a0001c0001t0007g0142a0001c0001t0011g0011others(12): Show | 17 | HG00733.hp1 HG01106.hp2 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.165+523dupT | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 43845121 | ||||||
| chr2:43845121 | A | T | 14 | a0001c0001t0007g0057a0001c0001t0017g0128a0001c0001t0031g0056others(11): Show | 15 | HG00280.hp1 HG00735.hp2 HG01069.hp1 others(12): Show |
intron_variant | MODIFIER | c.165+513A>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 2/12 | chr2 | 43845121 | |||||||
| chr2:43845184 | G | C | 11 | a0007c0009t0022g0005a0007c0009t0022g0032a0007c0009t0028g0033others(8): Show | 12 | HG01346.hp2 HG02109.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.165+576G>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 2/12 | chr2 | 43845184 | |||||||
| chr2:43845301 | G | A | 4 | a0003c0002t0021g0149a0003c0002t0021g0150a0003c0002t0021g0151others(1): Show | 5 | HG00642.hp2 HG01099.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.165+693G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 2/12 | chr2 | 43845301 | |||||||
| chr2:43845349 | C | A | 1 | a0002c0003t0090g0035 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.165+741C>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 2/12 | chr2 | 43845349 | |||||||
| chr2:43845412 | C | G | 4 | a0003c0002t0021g0149a0003c0002t0021g0150a0003c0002t0021g0151others(1): Show | 5 | HG00642.hp2 HG01099.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.166-743C>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 2/12 | chr2 | 43845412 | |||||||
| chr2:43845435 | G | C | 11 | a0007c0009t0022g0005a0007c0009t0022g0032a0007c0009t0028g0033others(8): Show | 12 | HG01346.hp2 HG02109.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.166-720G>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 2/12 | chr2 | 43845435 | |||||||
| chr2:43845437 | G | T | 260 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(257): Show | 279 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(276): Show |
intron_variant | MODIFIER | c.166-718G>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 2/12 | chr2 | 43845437 | |||||||
| chr2:43845487 | T | C | 11 | a0007c0009t0022g0005a0007c0009t0022g0032a0007c0009t0028g0033others(8): Show | 12 | HG01346.hp2 HG02109.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.166-668T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 2/12 | chr2 | 43845487 | |||||||
| chr2:43845748 | A | G | 6 | a0003c0002t0026g0041a0003c0002t0092g0040a0003c0010t0020g0036others(3): Show | 6 | HG01192.hp1 HG02895.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.166-407A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 2/12 | chr2 | 43845748 | |||||||
| chr2:43845811 | G | A | 1 | a0007c0020t0061g0029 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.166-344G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 2/12 | chr2 | 43845811 | |||||||
| chr2:43845827 | G | A | 11 | a0007c0009t0022g0005a0007c0009t0022g0032a0007c0009t0028g0033others(8): Show | 12 | HG01346.hp2 HG02109.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.166-328G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 2/12 | chr2 | 43845827 | |||||||
| chr2:43845852 | C | A | 4 | a0003c0002t0021g0149a0003c0002t0021g0150a0003c0002t0021g0151others(1): Show | 5 | HG00642.hp2 HG01099.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.166-303C>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 2/12 | chr2 | 43845852 | |||||||
| chr2:43845946 | T | C | 11 | a0007c0009t0022g0005a0007c0009t0022g0032a0007c0009t0028g0033others(8): Show | 12 | HG01346.hp2 HG02109.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.166-209T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 2/12 | chr2 | 43845946 | |||||||
| chr2:43846014 | G | A | 11 | a0007c0009t0022g0005a0007c0009t0022g0032a0007c0009t0028g0033others(8): Show | 12 | HG01346.hp2 HG02109.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.166-141G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 2/12 | chr2 | 43846014 | |||||||
| chr2:43846068 | C | T | 1 | a0007c0020t0061g0029 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.166-87C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 2/12 | chr2 | 43846068 | |||||||
| chr2:43846444 | G | C | 1 | a0001c0008t0050g0073 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.322+133G>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43846444 | |||||||
| chr2:43846454 | C | G | 1 | a0002c0003t0005g0257 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.322+143C>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43846454 | |||||||
| chr2:43846517 | T | C | 22 | a0002c0003t0039g0170a0003c0002t0004g0172a0003c0002t0095g0242others(19): Show | 23 | HG00438.hp1 HG00741.hp2 HG01943.hp1 others(20): Show |
intron_variant | MODIFIER | c.322+206T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43846517 | |||||||
| chr2:43846533 | G | A | 2 | a0008c0016t0044g0192a0008c0016t0044g0193 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.322+222G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43846533 | |||||||
| chr2:43846620 | A | T | 1 | a0003c0002t0092g0040 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.322+309A>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43846620 | |||||||
| chr2:43846679 | T | G | 2 | a0008c0016t0044g0192a0008c0016t0044g0193 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.322+368T>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43846679 | |||||||
| chr2:43846742 | T | C | 260 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(257): Show | 279 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(276): Show |
intron_variant | MODIFIER | c.322+431T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43846742 | |||||||
| chr2:43846813 | C | T | 1 | a0002c0003t0002g0255 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.322+502C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43846813 | |||||||
| chr2:43846814 | A | G | 1 | a0001c0001t0003g0122 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.322+503A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43846814 | |||||||
| chr2:43846861 | G | A | 17 | a0003c0002t0004g0172a0003c0021t0007g0030a0003c0022t0014g0261others(14): Show | 18 | HG00438.hp1 HG00741.hp2 HG01943.hp1 others(15): Show |
intron_variant | MODIFIER | c.322+550G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43846861 | |||||||
| chr2:43846936 | G | A | 2 | a0001c0001t0007g0142a0001c0008t0051g0141 | 2 | HG01123.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.322+625G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43846936 | |||||||
| chr2:43846980 | A | ACG | 3 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038 | 3 | HG01192.hp1 HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.322+676_322+677dup others(2): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 43846980 | ||||||
| chr2:43846987 | CGT | C | 26 | a0003c0002t0002g0209a0003c0002t0004g0172a0003c0002t0095g0242others(23): Show | 27 | HG00438.hp1 HG00741.hp2 HG01943.hp1 others(24): Show |
intron_variant | MODIFIER | c.322+678_322+679del others(2): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 43846987 | ||||||
| chr2:43846988 | GTGCA | G | 13 | a0003c0002t0018g0015a0003c0002t0018g0158a0003c0002t0018g0159others(10): Show | 15 | HG00642.hp2 HG01074.hp1 HG01099.hp1 others(12): Show |
intron_variant | MODIFIER | c.322+678_322+681del others(4): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43846988 | |||||||
| chr2:43846988 | GTGCACAC others(1): Show |
G | 4 | a0002c0003t0005g0257a0002c0003t0090g0035a0002c0026t0087g0198others(1): Show | 4 | HG02083.hp1 HG02300.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.322+678_322+685del others(8): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43846988 | |||||||
| chr2:43846988 | GTGCACAC others(3): Show |
G | 83 | a0002c0003t0002g0019a0002c0003t0002g0044a0002c0003t0002g0045others(80): Show | 89 | HG00280.hp2 HG00323.hp1 HG00621.hp1 others(86): Show |
intron_variant | MODIFIER | c.322+678_322+687del others(10): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43846988 | |||||||
| chr2:43846988 | GTGCACAC others(7): Show |
G | 1 | a0002c0003t0103g0194 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.322+678_322+691del others(14): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43846988 | |||||||
| chr2:43846989 | T | C | 18 | a0003c0002t0026g0041a0003c0002t0042g0016a0003c0002t0092g0040others(15): Show | 21 | HG01192.hp1 HG01346.hp2 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.322+678T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43846989 | |||||||
| chr2:43846990 | G | A | 3 | a0003c0002t0042g0016a0003c0002t0093g0161a0003c0014t0043g0217 | 4 | HG01884.hp2 HG02809.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.322+679G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43846990 | |||||||
| chr2:43846990 | G | GCA | 58 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0047others(55): Show | 62 | HG00099.hp1 HG00558.hp1 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.322+713_322+714dup others(2): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 43846990 | ||||||
| chr2:43846990 | G | GCACA | 8 | a0001c0001t0003g0134a0001c0001t0007g0145a0001c0001t0010g0060others(5): Show | 9 | HG00597.hp2 HG00673.hp1 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.322+711_322+714dup others(4): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 43846990 | ||||||
| chr2:43846990 | G | GCACACA | 7 | a0001c0001t0011g0125a0001c0001t0035g0053a0001c0001t0035g0054others(4): Show | 8 | HG02572.hp1 HG02647.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.322+709_322+714dup others(6): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 43846990 | ||||||
| chr2:43846990 | G | GCACACAC others(1): Show |
5 | a0001c0001t0011g0123a0001c0001t0011g0124a0007c0009t0022g0032others(2): Show | 5 | HG01346.hp2 HG02630.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.322+707_322+714dup others(8): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 43846990 | ||||||
| chr2:43846990 | G | GCACACAC others(3): Show |
1 | a0007c0009t0022g0005 | 2 | HG02486.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.322+705_322+714dup others(10): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 43846990 | ||||||
| chr2:43846990 | GCA | G | 22 | a0001c0001t0001g0116a0001c0001t0003g0051a0001c0001t0003g0111others(19): Show | 22 | HG00323.hp2 HG00597.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.322+713_322+714del others(2): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 43846990 | ||||||
| chr2:43846990 | GCACA | G | 4 | a0001c0001t0030g0119a0001c0001t0069g0129a0003c0002t0002g0287others(1): Show | 4 | HG01074.hp2 HG01433.hp2 HG02027.hp2 others(1): Show |
intron_variant | MODIFIER | c.322+711_322+714del others(4): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 43846990 | ||||||
| chr2:43846990 | GCACACA | G | 9 | a0001c0001t0003g0121a0001c0001t0010g0120a0001c0001t0017g0052others(6): Show | 9 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.322+709_322+714del others(6): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 43846990 | ||||||
| chr2:43846992 | A | G | 2 | a0007c0020t0061g0029a0010c0013t0099g0183 | 2 | HG03834.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.322+681A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43846992 | |||||||
| chr2:43846996 | A | G | 1 | a0001c0001t0007g0057 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.322+685A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43846996 | |||||||
| chr2:43846998 | A | G | 1 | a0002c0003t0090g0035 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.322+687A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43846998 | |||||||
| chr2:43847039 | A | T | 1 | a0003c0010t0020g0038 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.322+728A>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43847039 | |||||||
| chr2:43847121 | T | C | 1 | a0002c0003t0004g0222 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.322+810T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43847121 | |||||||
| chr2:43847219 | G | A | 1 | a0002c0003t0004g0222 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.322+908G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43847219 | |||||||
| chr2:43847289 | T | G | 1 | a0001c0001t0001g0096 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.322+978T>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43847289 | |||||||
| chr2:43847292 | C | T | 264 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(261): Show | 284 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(281): Show |
intron_variant | MODIFIER | c.322+981C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43847292 | |||||||
| chr2:43847325 | T | A | 3 | a0002c0003t0012g0177a0002c0003t0101g0178a0002c0004t0008g0213 | 3 | HG01884.hp1 HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.322+1014T>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43847325 | |||||||
| chr2:43847342 | T | C | 1 | a0002c0003t0002g0210 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.322+1031T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43847342 | |||||||
| chr2:43847413 | A | G | 3 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038 | 3 | HG01192.hp1 HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.322+1102A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43847413 | |||||||
| chr2:43847473 | C | T | 2 | a0003c0002t0042g0016a0003c0002t0093g0161 | 3 | HG01884.hp2 HG02809.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.322+1162C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43847473 | |||||||
| chr2:43847503 | C | G | 139 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(136): Show | 149 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(146): Show |
intron_variant | MODIFIER | c.322+1192C>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43847503 | |||||||
| chr2:43847508 | C | T | 1 | a0004c0006t0024g0043 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.322+1197C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43847508 | |||||||
| chr2:43847534 | C | T | 125 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(122): Show | 133 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(130): Show |
intron_variant | MODIFIER | c.322+1223C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43847534 | |||||||
| chr2:43847557 | A | T | 4 | a0003c0002t0095g0242a0003c0002t0104g0216a0003c0014t0043g0217others(1): Show | 4 | HG02717.hp1 HG02717.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.322+1246A>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43847557 | |||||||
| chr2:43847565 | G | C | 10 | a0003c0002t0002g0209a0003c0002t0018g0015a0003c0002t0018g0158others(7): Show | 11 | HG01074.hp1 HG01099.hp1 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.322+1254G>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43847565 | |||||||
| chr2:43847624 | G | A | 1 | a0002c0003t0103g0194 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.322+1313G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43847624 | |||||||
| chr2:43847719 | G | A | 1 | a0002c0003t0004g0223 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.322+1408G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43847719 | |||||||
| chr2:43847750 | G | GT | 5 | a0003c0002t0018g0015a0003c0002t0021g0149a0003c0002t0021g0150others(2): Show | 7 | HG00642.hp2 HG01074.hp1 HG01099.hp1 others(4): Show |
intron_variant | MODIFIER | c.322+1447dupT | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 43847750 | ||||||
| chr2:43847778 | T | C | 1 | a0003c0010t0110g0039 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.322+1467T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43847778 | |||||||
| chr2:43847845 | G | A | 2 | a0003c0010t0020g0036a0003c0010t0020g0037 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.322+1534G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43847845 | |||||||
| chr2:43847924 | C | A | 1 | a0002c0003t0036g0022 | 2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.322+1613C>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43847924 | |||||||
| chr2:43847927 | A | AT | 11 | a0007c0009t0022g0005a0007c0009t0022g0032a0007c0009t0028g0033others(8): Show | 12 | HG01346.hp2 HG02109.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.322+1625dupT | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 43847927 | ||||||
| chr2:43847954 | A | G | 140 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(137): Show | 150 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(147): Show |
intron_variant | MODIFIER | c.322+1643A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43847954 | |||||||
| chr2:43848023 | T | C | 141 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(138): Show | 152 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(149): Show |
intron_variant | MODIFIER | c.322+1712T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43848023 | |||||||
| chr2:43848078 | T | A | 4 | a0003c0002t0002g0275a0003c0002t0002g0283a0003c0002t0002g0284others(1): Show | 4 | HG00642.hp1 HG00735.hp1 HG01167.hp2 others(1): Show |
intron_variant | MODIFIER | c.322+1767T>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43848078 | |||||||
| chr2:43848251 | C | G | 1 | a0001c0001t0007g0118 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.322+1940C>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43848251 | |||||||
| chr2:43848344 | T | C | 17 | a0003c0002t0004g0172a0003c0021t0007g0030a0003c0022t0014g0261others(14): Show | 18 | HG00438.hp1 HG00741.hp2 HG01943.hp1 others(15): Show |
intron_variant | MODIFIER | c.322+2033T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43848344 | |||||||
| chr2:43848407 | T | G | 1 | a0002c0003t0005g0257 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.322+2096T>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43848407 | |||||||
| chr2:43848596 | A | G | 4 | a0003c0002t0021g0149a0003c0002t0021g0150a0003c0002t0021g0151others(1): Show | 5 | HG00642.hp2 HG01099.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.322+2285A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43848596 | |||||||
| chr2:43848670 | C | G | 1 | a0003c0002t0104g0216 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.322+2359C>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43848670 | |||||||
| chr2:43848756 | C | T | 1 | a0003c0002t0026g0041 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.322+2445C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43848756 | |||||||
| chr2:43848813 | C | G | 1 | a0001c0001t0003g0122 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.322+2502C>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43848813 | |||||||
| chr2:43848831 | C | T | 1 | a0012c0031t0045g0025 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.322+2520C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43848831 | |||||||
| chr2:43848853 | TA | T | 11 | a0002c0003t0090g0035a0003c0002t0002g0209a0003c0002t0018g0015others(8): Show | 12 | HG01074.hp1 HG01099.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.322+2552delA | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 43848853 | ||||||
| chr2:43848882 | C | T | 1 | a0003c0014t0043g0217 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.322+2571C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43848882 | |||||||
| chr2:43848928 | G | A | 1 | a0002c0004t0009g0185 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.322+2617G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43848928 | |||||||
| chr2:43849021 | T | TA | 21 | a0001c0001t0003g0075a0001c0001t0003g0111a0001c0001t0011g0123others(18): Show | 23 | HG01884.hp2 HG01891.hp1 HG01928.hp1 others(20): Show |
intron_variant | MODIFIER | c.323-2538dupA | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 43849021 | ||||||
| chr2:43849021 | T | TAAA | 11 | a0003c0002t0026g0041a0007c0009t0022g0005a0007c0009t0022g0032others(8): Show | 12 | HG01346.hp2 HG02109.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.323-2540_323-2538d others(5): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 43849021 | ||||||
| chr2:43849021 | TA | T | 18 | a0001c0001t0001g0048a0001c0001t0001g0094a0001c0001t0003g0059others(15): Show | 18 | HG00323.hp1 HG01515.hp1 HG01515.hp2 others(15): Show |
intron_variant | MODIFIER | c.323-2538delA | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 43849021 | ||||||
| chr2:43849021 | TAAAAAAA | T | 10 | a0003c0002t0002g0264a0003c0002t0002g0282a0003c0002t0002g0287others(7): Show | 10 | HG00099.hp2 HG00741.hp1 HG01070.hp2 others(7): Show |
intron_variant | MODIFIER | c.323-2544_323-2538d others(9): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 43849021 | ||||||
| chr2:43849021 | TAAAAAAA others(3): Show |
T | 1 | a0003c0002t0019g0063 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.323-2547_323-2538d others(12): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 43849021 | ||||||
| chr2:43849105 | C | G | 10 | a0002c0003t0090g0035a0003c0002t0026g0041a0003c0002t0092g0040others(7): Show | 11 | HG01192.hp1 HG02647.hp2 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.323-2479C>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43849105 | |||||||
| chr2:43849217 | G | A | 3 | a0006c0005t0004g0219a0006c0005t0004g0244a0006c0005t0004g0259 | 3 | HG03098.hp2 HG03209.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.323-2367G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43849217 | |||||||
| chr2:43849283 | CTCAGAGT | C | 90 | a0001c0001t0001g0002a0001c0001t0001g0047a0001c0001t0001g0069others(87): Show | 98 | HG00280.hp2 HG00323.hp1 HG00558.hp2 others(95): Show |
intron_variant | MODIFIER | c.323-2298_323-2292d others(9): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 43849283 | ||||||
| chr2:43849490 | A | G | 6 | a0002c0003t0090g0035a0008c0015t0012g0017a0008c0016t0044g0192others(3): Show | 7 | HG02809.hp1 HG02896.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.323-2094A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43849490 | |||||||
| chr2:43849583 | TCTCCCCA others(7): Show |
T | 2 | a0001c0008t0015g0076a0001c0008t0015g0077 | 2 | HG03490.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.323-1999_323-1986d others(16): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 43849583 | ||||||
| chr2:43849592 | A | G | 10 | a0003c0002t0002g0209a0003c0002t0018g0015a0003c0002t0018g0158others(7): Show | 11 | HG01074.hp1 HG01099.hp1 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.323-1992A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43849592 | |||||||
| chr2:43849713 | T | C | 1 | a0003c0002t0104g0216 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.323-1871T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43849713 | |||||||
| chr2:43849933 | C | G | 12 | a0003c0002t0026g0041a0007c0009t0022g0005a0007c0009t0022g0032others(9): Show | 13 | HG01346.hp2 HG02109.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.323-1651C>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43849933 | |||||||
| chr2:43850010 | G | A | 3 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0099 | 3 | HG02735.hp1 HG03017.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.323-1574G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43850010 | |||||||
| chr2:43850032 | G | A | 1 | a0006c0005t0027g0220 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.323-1552G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43850032 | |||||||
| chr2:43850086 | T | C | 291 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(288): Show | 311 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(308): Show |
intron_variant | MODIFIER | c.323-1498T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43850086 | |||||||
| chr2:43850184 | C | T | 3 | a0010c0013t0002g0167a0010c0013t0005g0168a0010c0013t0099g0183 | 3 | HG01943.hp1 HG01975.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.323-1400C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43850184 | |||||||
| chr2:43850314 | T | C | 294 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(291): Show | 314 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(311): Show |
intron_variant | MODIFIER | c.323-1270T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43850314 | |||||||
| chr2:43850501 | A | G | 1 | a0005c0007t0006g0109 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.323-1083A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43850501 | |||||||
| chr2:43850545 | T | C | 1 | a0008c0015t0012g0017 | 2 | HG06807.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.323-1039T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43850545 | |||||||
| chr2:43850603 | A | G | 1 | a0001c0001t0011g0124 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.323-981A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43850603 | |||||||
| chr2:43850629 | C | T | 179 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0048others(176): Show | 191 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(188): Show |
intron_variant | MODIFIER | c.323-955C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43850629 | |||||||
| chr2:43850909 | C | CA | 7 | a0001c0001t0015g0065a0001c0001t0056g0092a0001c0008t0051g0141others(4): Show | 7 | HG01255.hp2 HG02055.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.323-658dupA | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 43850909 | ||||||
| chr2:43850921 | A | G | 1 | a0001c0001t0001g0091 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.323-663A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43850921 | |||||||
| chr2:43851023 | A | G | 135 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0048others(132): Show | 142 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(139): Show |
intron_variant | MODIFIER | c.323-561A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43851023 | |||||||
| chr2:43851053 | T | C | 5 | a0003c0002t0004g0172a0003c0010t0020g0036a0003c0010t0020g0037others(2): Show | 5 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.323-531T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43851053 | |||||||
| chr2:43851079 | G | C | 2 | a0002c0003t0098g0171a0009c0012t0023g0026 | 2 | NA19043.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.323-505G>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43851079 | |||||||
| chr2:43851209 | C | T | 2 | a0003c0002t0042g0016a0003c0002t0093g0161 | 3 | HG01884.hp2 HG02809.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.323-375C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43851209 | |||||||
| chr2:43851260 | C | G | 5 | a0009c0012t0023g0026a0009c0012t0023g0027a0009c0012t0023g0028others(2): Show | 5 | HG02109.hp2 HG02559.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.323-324C>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43851260 | |||||||
| chr2:43851356 | C | T | 1 | a0001c0001t0069g0129 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.323-228C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43851356 | |||||||
| chr2:43851384 | G | A | 1 | a0001c0001t0067g0112 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.323-200G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43851384 | |||||||
| chr2:43851449 | C | T | 2 | a0003c0002t0042g0016a0003c0002t0093g0161 | 3 | HG01884.hp2 HG02809.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.323-135C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43851449 | |||||||
| chr2:43851537 | C | A | 6 | a0007c0009t0022g0005a0007c0009t0022g0032a0007c0009t0028g0033others(3): Show | 7 | HG01346.hp2 HG02486.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.323-47C>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43851537 | |||||||
| chr2:43851574 | G | A | 1 | a0014c0025t0074g0156 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.323-10G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 3/12 | chr2 | 43851574 | |||||||
| chr2:43851865 | T | C | 181 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0048others(178): Show | 193 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(190): Show |
intron_variant | MODIFIER | c.561+43T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 4/12 | chr2 | 43851865 | |||||||
| chr2:43852061 | G | A | 2 | a0003c0002t0042g0016a0003c0002t0093g0161 | 3 | HG01884.hp2 HG02809.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.561+239G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 4/12 | chr2 | 43852061 | |||||||
| chr2:43852150 | C | T | 5 | a0009c0012t0023g0026a0009c0012t0023g0027a0009c0012t0023g0028others(2): Show | 5 | HG02109.hp2 HG02559.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.562-204C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 4/12 | chr2 | 43852150 | |||||||
| chr2:43852164 | C | T | 1 | a0001c0001t0001g0096 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.562-190C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 4/12 | chr2 | 43852164 | |||||||
| chr2:43852169 | C | T | 1 | a0001c0001t0071g0108 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.562-185C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 4/12 | chr2 | 43852169 | |||||||
| chr2:43852171 | C | A | 29 | a0003c0002t0004g0172a0003c0002t0026g0041a0003c0021t0007g0030others(26): Show | 31 | HG00438.hp1 HG00741.hp2 HG01346.hp2 others(28): Show |
intron_variant | MODIFIER | c.562-183C>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 4/12 | chr2 | 43852171 | |||||||
| chr2:43852177 | G | C | 1 | a0002c0003t0005g0257 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.562-177G>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 4/12 | chr2 | 43852177 | |||||||
| chr2:43852262 | G | A | 24 | a0001c0001t0001g0002a0001c0001t0001g0047a0001c0001t0001g0069others(21): Show | 26 | HG00323.hp1 HG00558.hp2 HG00621.hp1 others(23): Show |
intron_variant | MODIFIER | c.562-92G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 4/12 | chr2 | 43852262 | |||||||
| chr2:43852269 | C | T | 1 | a0003c0002t0008g0176 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.562-85C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 4/12 | chr2 | 43852269 | |||||||
| chr2:43852532 | C | T | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.694+46C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 5/12 | chr2 | 43852532 | |||||||
| chr2:43852581 | CCT | C | 5 | a0009c0012t0023g0026a0009c0012t0023g0027a0009c0012t0023g0028others(2): Show | 5 | HG02109.hp2 HG02559.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.695-13_695-12delCT | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 43852581 | ||||||
| chr2:43852914 | C | T | 3 | a0003c0011t0012g0001a0003c0011t0012g0061a0003c0011t0091g0001 | 4 | HG02647.hp2 HG03130.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.964+46C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43852914 | |||||||
| chr2:43852946 | G | GAAAGATT others(312): Show |
4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+94_964+95insGG others(317): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 43852946 | ||||||
| chr2:43852991 | G | A | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+123G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43852991 | |||||||
| chr2:43853046 | G | A | 2 | a0003c0002t0002g0175a0003c0002t0102g0207 | 2 | HG00639.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.964+178G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43853046 | |||||||
| chr2:43853103 | A | G | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+235A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43853103 | |||||||
| chr2:43853171 | C | T | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+303C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43853171 | |||||||
| chr2:43853185 | A | G | 41 | a0003c0002t0001g0021a0003c0002t0001g0189a0003c0002t0001g0214others(38): Show | 44 | HG00438.hp1 HG00741.hp2 HG01192.hp1 others(41): Show |
intron_variant | MODIFIER | c.964+317A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43853185 | |||||||
| chr2:43853200 | T | A | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+332T>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43853200 | |||||||
| chr2:43853338 | C | T | 1 | a0004c0006t0040g0241 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.964+470C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43853338 | |||||||
| chr2:43853366 | G | C | 1 | a0002c0003t0005g0257 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.964+498G>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43853366 | |||||||
| chr2:43853499 | G | A | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+631G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43853499 | |||||||
| chr2:43853517 | C | T | 1 | a0001c0001t0003g0107 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.964+649C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43853517 | |||||||
| chr2:43853541 | T | TA | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+674dupA | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 43853541 | ||||||
| chr2:43853576 | C | T | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+708C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43853576 | |||||||
| chr2:43853660 | A | T | 3 | a0003c0011t0012g0001a0003c0011t0012g0061a0003c0011t0091g0001 | 4 | HG02647.hp2 HG03130.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.964+792A>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43853660 | |||||||
| chr2:43853700 | C | T | 3 | a0002c0004t0008g0270a0002c0004t0008g0271a0002c0004t0008g0272 | 3 | HG00323.hp1 HG01109.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.964+832C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43853700 | |||||||
| chr2:43853748 | T | C | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+880T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43853748 | |||||||
| chr2:43853750 | G | A | 1 | a0002c0003t0005g0257 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.964+882G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43853750 | |||||||
| chr2:43853752 | A | G | 3 | a0003c0011t0012g0001a0003c0011t0012g0061a0003c0011t0091g0001 | 4 | HG02647.hp2 HG03130.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.964+884A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43853752 | |||||||
| chr2:43853828 | G | A | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+960G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43853828 | |||||||
| chr2:43853903 | T | C | 189 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(186): Show | 204 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(201): Show |
intron_variant | MODIFIER | c.964+1035T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43853903 | |||||||
| chr2:43853953 | C | A | 80 | a0002c0003t0002g0019a0002c0003t0002g0044a0002c0003t0002g0045others(77): Show | 85 | HG00280.hp2 HG00323.hp1 HG00621.hp1 others(82): Show |
intron_variant | MODIFIER | c.964+1085C>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43853953 | |||||||
| chr2:43854041 | G | A | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+1173G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43854041 | |||||||
| chr2:43854052 | C | T | 73 | a0002c0003t0002g0019a0002c0003t0002g0044a0002c0003t0002g0045others(70): Show | 77 | HG00280.hp2 HG00323.hp1 HG00621.hp1 others(74): Show |
intron_variant | MODIFIER | c.964+1184C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43854052 | |||||||
| chr2:43854111 | A | G | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+1243A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43854111 | |||||||
| chr2:43854156 | C | T | 1 | a0002c0004t0008g0213 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.964+1288C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43854156 | |||||||
| chr2:43854226 | T | G | 5 | a0002c0003t0090g0035a0003c0010t0020g0036a0003c0010t0020g0037others(2): Show | 5 | HG01192.hp1 HG02809.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.964+1358T>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43854226 | |||||||
| chr2:43854287 | T | A | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+1419T>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43854287 | |||||||
| chr2:43854296 | C | G | 1 | a0001c0001t0017g0128 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.964+1428C>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43854296 | |||||||
| chr2:43854349 | C | T | 134 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0048others(131): Show | 141 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(138): Show |
intron_variant | MODIFIER | c.964+1481C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43854349 | |||||||
| chr2:43854436 | T | A | 1 | a0002c0003t0005g0257 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.964+1568T>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43854436 | |||||||
| chr2:43854488 | T | G | 39 | a0002c0003t0005g0196a0002c0003t0005g0230a0003c0002t0001g0021others(36): Show | 42 | HG00438.hp1 HG00741.hp2 HG01346.hp2 others(39): Show |
intron_variant | MODIFIER | c.964+1620T>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43854488 | |||||||
| chr2:43854498 | T | A | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+1630T>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43854498 | |||||||
| chr2:43854534 | C | T | 5 | a0003c0002t0021g0149a0003c0002t0021g0150a0003c0002t0021g0151others(2): Show | 6 | HG00642.hp2 HG01099.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.964+1666C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43854534 | |||||||
| chr2:43854626 | C | CA | 147 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(144): Show | 159 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(156): Show |
intron_variant | MODIFIER | c.964+1777dupA | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 43854626 | ||||||
| chr2:43854626 | C | CAA | 8 | a0001c0001t0001g0097a0001c0008t0073g0078a0003c0002t0021g0149others(5): Show | 9 | HG00642.hp2 HG01099.hp2 HG01981.hp1 others(6): Show |
intron_variant | MODIFIER | c.964+1776_964+1777d others(4): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 43854626 | ||||||
| chr2:43854640 | A | AG | 5 | a0009c0012t0023g0026a0009c0012t0023g0027a0009c0012t0023g0028others(2): Show | 5 | HG02109.hp2 HG02559.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.964+1772_964+1773i others(3): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43854640 | |||||||
| chr2:43854759 | C | A | 3 | a0003c0011t0012g0001a0003c0011t0012g0061a0003c0011t0091g0001 | 4 | HG02647.hp2 HG03130.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.964+1891C>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43854759 | |||||||
| chr2:43854837 | C | T | 1 | a0002c0003t0039g0170 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.964+1969C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43854837 | |||||||
| chr2:43854919 | G | T | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+2051G>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43854919 | |||||||
| chr2:43854972 | G | T | 1 | a0001c0001t0016g0106 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.964+2104G>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43854972 | |||||||
| chr2:43854979 | C | T | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+2111C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43854979 | |||||||
| chr2:43855170 | C | G | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+2302C>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43855170 | |||||||
| chr2:43855212 | A | G | 3 | a0002c0003t0002g0019a0002c0003t0094g0019a0002c0003t0096g0184 | 3 | HG00738.hp1 HG02572.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.964+2344A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43855212 | |||||||
| chr2:43855218 | A | G | 1 | a0002c0004t0014g0179 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.964+2350A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43855218 | |||||||
| chr2:43855223 | A | G | 142 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(139): Show | 151 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(148): Show |
intron_variant | MODIFIER | c.964+2355A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43855223 | |||||||
| chr2:43855334 | C | T | 4 | a0003c0002t0095g0242a0003c0002t0104g0216a0003c0014t0043g0217others(1): Show | 4 | HG02717.hp1 HG02717.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+2466C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43855334 | |||||||
| chr2:43855414 | C | G | 5 | a0002c0003t0090g0035a0003c0010t0020g0036a0003c0010t0020g0037others(2): Show | 5 | HG01192.hp1 HG02809.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.964+2546C>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43855414 | |||||||
| chr2:43855504 | A | C | 2 | a0002c0003t0012g0177a0002c0003t0101g0178 | 2 | HG01884.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.964+2636A>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43855504 | |||||||
| chr2:43855530 | T | A | 142 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(139): Show | 151 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(148): Show |
intron_variant | MODIFIER | c.964+2662T>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43855530 | |||||||
| chr2:43855550 | G | C | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+2682G>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43855550 | |||||||
| chr2:43855564 | C | T | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+2696C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43855564 | |||||||
| chr2:43855568 | C | A | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+2700C>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43855568 | |||||||
| chr2:43855572 | A | G | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+2704A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43855572 | |||||||
| chr2:43855576 | A | G | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+2708A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43855576 | |||||||
| chr2:43855718 | C | T | 1 | a0002c0003t0012g0147 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.964+2850C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43855718 | |||||||
| chr2:43855755 | C | T | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+2887C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43855755 | |||||||
| chr2:43855763 | T | C | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+2895T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43855763 | |||||||
| chr2:43855779 | A | T | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+2911A>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43855779 | |||||||
| chr2:43855840 | G | A | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+2972G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43855840 | |||||||
| chr2:43855880 | C | A | 137 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(134): Show | 146 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(143): Show |
intron_variant | MODIFIER | c.964+3012C>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43855880 | |||||||
| chr2:43855930 | C | T | 1 | a0001c0001t0003g0075 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.964+3062C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43855930 | |||||||
| chr2:43855961 | TCTCA | T | 2 | a0003c0002t0042g0016a0003c0002t0093g0161 | 3 | HG01884.hp2 HG02809.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.964+3096_964+3099d others(6): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 43855961 | ||||||
| chr2:43855984 | T | C | 126 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(123): Show | 134 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(131): Show |
intron_variant | MODIFIER | c.964+3116T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43855984 | |||||||
| chr2:43855988 | T | C | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+3120T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43855988 | |||||||
| chr2:43856137 | T | C | 2 | a0001c0001t0034g0079a0001c0001t0034g0093 | 2 | HG02135.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.964+3269T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43856137 | |||||||
| chr2:43856210 | G | A | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+3342G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43856210 | |||||||
| chr2:43856237 | G | C | 1 | a0002c0003t0098g0171 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.964+3369G>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43856237 | |||||||
| chr2:43856285 | A | G | 1 | a0009c0012t0072g0024 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.964+3417A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43856285 | |||||||
| chr2:43856331 | TCCCTGTC others(17): Show |
T | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+3487_964+3510d others(26): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 43856331 | ||||||
| chr2:43856355 | A | T | 137 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(134): Show | 146 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(143): Show |
intron_variant | MODIFIER | c.964+3487A>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43856355 | |||||||
| chr2:43856405 | T | C | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+3537T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43856405 | |||||||
| chr2:43856515 | G | A | 137 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(134): Show | 146 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(143): Show |
intron_variant | MODIFIER | c.964+3647G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43856515 | |||||||
| chr2:43856518 | C | CTCTCACT others(13): Show |
1 | a0003c0017t0007g0014 | 2 | HG00642.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.964+3662_964+3681d others(22): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 43856518 | ||||||
| chr2:43856588 | C | T | 1 | a0001c0001t0001g0096 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.964+3720C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43856588 | |||||||
| chr2:43856616 | T | C | 2 | a0003c0002t0042g0016a0003c0002t0093g0161 | 3 | HG01884.hp2 HG02809.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.964+3748T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43856616 | |||||||
| chr2:43856623 | C | CTCTA | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+3758_964+3761d others(6): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 43856623 | ||||||
| chr2:43856665 | A | G | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+3797A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43856665 | |||||||
| chr2:43856713 | A | G | 2 | a0003c0002t0004g0172a0003c0022t0014g0261 | 2 | HG02818.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.964+3845A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43856713 | |||||||
| chr2:43856744 | G | C | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+3876G>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43856744 | |||||||
| chr2:43856746 | T | C | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+3878T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43856746 | |||||||
| chr2:43856826 | C | A | 1 | a0005c0007t0053g0155 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.964+3958C>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43856826 | |||||||
| chr2:43856863 | G | A | 1 | a0003c0002t0092g0040 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.964+3995G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43856863 | |||||||
| chr2:43856873 | T | C | 3 | a0006c0005t0004g0219a0006c0005t0004g0244a0006c0005t0004g0259 | 3 | HG03098.hp2 HG03209.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.964+4005T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43856873 | |||||||
| chr2:43856913 | T | C | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+4045T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43856913 | |||||||
| chr2:43856973 | A | G | 1 | a0003c0002t0076g0238 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.964+4105A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43856973 | |||||||
| chr2:43857023 | C | A | 5 | a0003c0002t0021g0149a0003c0002t0021g0150a0003c0002t0021g0151others(2): Show | 6 | HG00642.hp2 HG01099.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.964+4155C>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43857023 | |||||||
| chr2:43857041 | C | A | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+4173C>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43857041 | |||||||
| chr2:43857050 | A | T | 194 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(191): Show | 210 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(207): Show |
intron_variant | MODIFIER | c.964+4182A>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43857050 | |||||||
| chr2:43857117 | A | AGATAGAA others(37): Show |
4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+4273_964+4274i others(46): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 43857117 | ||||||
| chr2:43857117 | AGATAGAA others(37): Show |
A | 1 | a0002c0003t0004g0222 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.964+4276_964+4319d others(46): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 43857117 | ||||||
| chr2:43857133 | A | G | 12 | a0003c0002t0026g0041a0007c0009t0022g0005a0007c0009t0022g0032others(9): Show | 13 | HG01346.hp2 HG02109.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.964+4265A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43857133 | |||||||
| chr2:43857140 | T | C | 1 | a0001c0001t0001g0100 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.964+4272T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43857140 | |||||||
| chr2:43857177 | A | G | 2 | a0003c0002t0042g0016a0003c0002t0093g0161 | 3 | HG01884.hp2 HG02809.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.964+4309A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43857177 | |||||||
| chr2:43857193 | T | C | 5 | a0009c0012t0023g0026a0009c0012t0023g0027a0009c0012t0023g0028others(2): Show | 5 | HG02109.hp2 HG02559.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.964+4325T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43857193 | |||||||
| chr2:43857328 | C | T | 2 | a0001c0008t0029g0152a0001c0008t0050g0073 | 2 | HG02055.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.964+4460C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43857328 | |||||||
| chr2:43857345 | T | A | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+4477T>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43857345 | |||||||
| chr2:43857351 | A | C | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+4483A>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43857351 | |||||||
| chr2:43857364 | A | T | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+4496A>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43857364 | |||||||
| chr2:43857422 | G | GATAGAAC others(31): Show |
2 | a0003c0002t0042g0016a0003c0002t0093g0161 | 3 | HG01884.hp2 HG02809.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.964+4573_964+4610d others(40): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 43857422 | ||||||
| chr2:43857461 | A | T | 24 | a0003c0002t0001g0021a0003c0002t0001g0189a0003c0002t0001g0214others(21): Show | 26 | HG00741.hp2 HG01943.hp1 HG01975.hp2 others(23): Show |
intron_variant | MODIFIER | c.964+4593A>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43857461 | |||||||
| chr2:43857547 | A | T | 3 | a0002c0003t0012g0177a0002c0003t0101g0178a0002c0004t0008g0213 | 3 | HG01884.hp1 HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.964+4679A>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43857547 | |||||||
| chr2:43857549 | A | G | 2 | a0002c0003t0002g0044a0002c0003t0002g0045 | 2 | HG01123.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.964+4681A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43857549 | |||||||
| chr2:43857726 | C | G | 1 | a0004c0006t0025g0277 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.964+4858C>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43857726 | |||||||
| chr2:43857836 | C | T | 26 | a0002c0003t0002g0044a0002c0003t0002g0045a0002c0003t0002g0200others(23): Show | 28 | HG00280.hp2 HG01070.hp1 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.964+4968C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43857836 | |||||||
| chr2:43857872 | C | T | 1 | a0001c0001t0001g0105 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.964+5004C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43857872 | |||||||
| chr2:43857873 | G | A | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+5005G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43857873 | |||||||
| chr2:43857896 | C | A | 3 | a0003c0002t0002g0275a0003c0002t0002g0283a0003c0002t0002g0284 | 3 | HG00735.hp1 HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.964+5028C>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43857896 | |||||||
| chr2:43857955 | G | T | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+5087G>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43857955 | |||||||
| chr2:43858025 | T | A | 8 | a0001c0001t0001g0070a0001c0001t0001g0072a0001c0001t0001g0080others(5): Show | 8 | HG01081.hp2 HG02080.hp1 HG02165.hp2 others(5): Show |
intron_variant | MODIFIER | c.964+5157T>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43858025 | |||||||
| chr2:43858105 | A | G | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+5237A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43858105 | |||||||
| chr2:43858127 | T | C | 137 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(134): Show | 146 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(143): Show |
intron_variant | MODIFIER | c.964+5259T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43858127 | |||||||
| chr2:43858402 | C | T | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+5534C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43858402 | |||||||
| chr2:43858500 | A | G | 4 | a0003c0002t0001g0021a0003c0002t0001g0189a0003c0002t0001g0214others(1): Show | 5 | NA18939.hp2 NA18957.hp1 NA18974.hp2 others(2): Show |
intron_variant | MODIFIER | c.964+5632A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43858500 | |||||||
| chr2:43858507 | T | C | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+5639T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43858507 | |||||||
| chr2:43858567 | C | A | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+5699C>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43858567 | |||||||
| chr2:43858724 | G | A | 1 | a0008c0018t0002g0174 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.964+5856G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43858724 | |||||||
| chr2:43858741 | A | AC | 138 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(135): Show | 147 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(144): Show |
intron_variant | MODIFIER | c.964+5874dupC | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 43858741 | ||||||
| chr2:43858849 | A | C | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+5981A>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43858849 | |||||||
| chr2:43858988 | C | A | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+6120C>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43858988 | |||||||
| chr2:43859008 | G | A | 3 | a0002c0003t0012g0177a0002c0003t0101g0178a0002c0004t0008g0213 | 3 | HG01884.hp1 HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.964+6140G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43859008 | |||||||
| chr2:43859082 | C | A | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+6214C>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43859082 | |||||||
| chr2:43859084 | G | C | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+6216G>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43859084 | |||||||
| chr2:43859180 | ACTGT | A | 12 | a0003c0002t0026g0041a0007c0009t0022g0005a0007c0009t0022g0032others(9): Show | 13 | HG01346.hp2 HG02109.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.964+6315_964+6318d others(6): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 43859180 | ||||||
| chr2:43859201 | C | G | 1 | a0001c0001t0070g0090 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.964+6333C>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43859201 | |||||||
| chr2:43859207 | C | T | 2 | a0004c0006t0040g0241a0004c0006t0040g0254 | 2 | HG01346.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.964+6339C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43859207 | |||||||
| chr2:43859300 | G | T | 1 | a0001c0001t0007g0089 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.964+6432G>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43859300 | |||||||
| chr2:43859423 | A | G | 1 | a0013c0029t0066g0126 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.964+6555A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43859423 | |||||||
| chr2:43859452 | G | A | 24 | a0003c0002t0001g0021a0003c0002t0001g0189a0003c0002t0001g0214others(21): Show | 26 | HG00741.hp2 HG01943.hp1 HG01975.hp2 others(23): Show |
intron_variant | MODIFIER | c.964+6584G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43859452 | |||||||
| chr2:43859535 | C | T | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+6667C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43859535 | |||||||
| chr2:43859584 | G | A | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+6716G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43859584 | |||||||
| chr2:43859656 | G | T | 117 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(114): Show | 123 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(120): Show |
intron_variant | MODIFIER | c.964+6788G>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43859656 | |||||||
| chr2:43859776 | G | A | 1 | a0002c0003t0004g0222 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.964+6908G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43859776 | |||||||
| chr2:43859824 | T | A | 1 | a0002c0003t0004g0199 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.964+6956T>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43859824 | |||||||
| chr2:43859885 | C | G | 24 | a0003c0002t0001g0021a0003c0002t0001g0189a0003c0002t0001g0214others(21): Show | 26 | HG00741.hp2 HG01943.hp1 HG01975.hp2 others(23): Show |
intron_variant | MODIFIER | c.964+7017C>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43859885 | |||||||
| chr2:43859929 | C | G | 2 | a0003c0002t0042g0016a0003c0002t0093g0161 | 3 | HG01884.hp2 HG02809.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.964+7061C>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43859929 | |||||||
| chr2:43860007 | C | G | 2 | a0003c0002t0042g0016a0003c0002t0093g0161 | 3 | HG01884.hp2 HG02809.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.964+7139C>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43860007 | |||||||
| chr2:43860019 | G | A | 2 | a0005c0007t0006g0006a0005c0007t0006g0064 | 3 | HG00280.hp1 HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.964+7151G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43860019 | |||||||
| chr2:43860077 | CCCTCTGG others(33): Show |
C | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+7218_964+7257d others(42): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 43860077 | ||||||
| chr2:43860168 | G | A | 1 | a0001c0001t0007g0142 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.964+7300G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43860168 | |||||||
| chr2:43860169 | A | G | 1 | a0001c0001t0001g0140 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.964+7301A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43860169 | |||||||
| chr2:43860234 | A | G | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+7366A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43860234 | |||||||
| chr2:43860347 | A | ACTAT | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+7480_964+7483d others(6): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 43860347 | ||||||
| chr2:43860352 | T | C | 142 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(139): Show | 151 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(148): Show |
intron_variant | MODIFIER | c.964+7484T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43860352 | |||||||
| chr2:43860385 | TCA | T | 5 | a0009c0012t0023g0026a0009c0012t0023g0027a0009c0012t0023g0028others(2): Show | 5 | HG02109.hp2 HG02559.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.964+7519_964+7520d others(4): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 43860385 | ||||||
| chr2:43860404 | G | A | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+7536G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43860404 | |||||||
| chr2:43860412 | G | T | 5 | a0007c0009t0022g0005a0007c0009t0022g0032a0007c0009t0028g0033others(2): Show | 6 | HG01346.hp2 HG02486.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.964+7544G>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43860412 | |||||||
| chr2:43860473 | A | G | 3 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038 | 3 | HG01192.hp1 HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.964+7605A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43860473 | |||||||
| chr2:43860501 | A | G | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+7633A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43860501 | |||||||
| chr2:43860608 | T | C | 8 | a0001c0001t0001g0070a0001c0001t0001g0072a0001c0001t0001g0080others(5): Show | 8 | HG01081.hp2 HG02080.hp1 HG02165.hp2 others(5): Show |
intron_variant | MODIFIER | c.964+7740T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43860608 | |||||||
| chr2:43860711 | C | A | 1 | a0002c0003t0002g0197 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.964+7843C>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43860711 | |||||||
| chr2:43860721 | G | A | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+7853G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43860721 | |||||||
| chr2:43860777 | GCTGTATA others(37): Show |
G | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+7942_964+7985d others(46): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 43860777 | ||||||
| chr2:43860824 | G | T | 1 | a0001c0008t0015g0144 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.964+7956G>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43860824 | |||||||
| chr2:43860843 | T | C | 3 | a0001c0001t0003g0058a0001c0001t0003g0059a0001c0001t0003g0139 | 3 | NA18962.hp2 NA18982.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.964+7975T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43860843 | |||||||
| chr2:43860894 | C | G | 4 | a0001c0001t0033g0138a0001c0001t0070g0090a0001c0008t0015g0076others(1): Show | 4 | HG03490.hp2 HG03704.hp1 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.964+8026C>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43860894 | |||||||
| chr2:43860902 | C | CTATCTGG others(37): Show |
20 | a0003c0002t0001g0021a0003c0002t0001g0189a0003c0002t0001g0214others(17): Show | 22 | HG00438.hp1 HG00741.hp2 HG01943.hp1 others(19): Show |
intron_variant | MODIFIER | c.964+8045_964+8088d others(46): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 43860902 | ||||||
| chr2:43860934 | A | T | 4 | a0001c0001t0007g0145a0001c0001t0010g0060a0001c0001t0030g0117others(1): Show | 4 | HG00597.hp1 HG00673.hp1 HG02015.hp2 others(1): Show |
intron_variant | MODIFIER | c.964+8066A>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43860934 | |||||||
| chr2:43860957 | T | G | 4 | a0003c0002t0095g0242a0003c0002t0104g0216a0003c0014t0043g0217others(1): Show | 4 | HG02717.hp1 HG02717.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+8089T>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43860957 | |||||||
| chr2:43861008 | A | G | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+8140A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43861008 | |||||||
| chr2:43861014 | T | A | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+8146T>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43861014 | |||||||
| chr2:43861026 | C | G | 5 | a0009c0012t0023g0026a0009c0012t0023g0027a0009c0012t0023g0028others(2): Show | 5 | HG02109.hp2 HG02559.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.964+8158C>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43861026 | |||||||
| chr2:43861028 | A | G | 117 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(114): Show | 123 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(120): Show |
intron_variant | MODIFIER | c.964+8160A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43861028 | |||||||
| chr2:43861039 | T | C | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+8171T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43861039 | |||||||
| chr2:43861057 | G | T | 2 | a0003c0021t0007g0030a0006c0005t0002g0260 | 2 | HG00741.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.964+8189G>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43861057 | |||||||
| chr2:43861064 | C | G | 3 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038 | 3 | HG01192.hp1 HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.964+8196C>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43861064 | |||||||
| chr2:43861123 | T | C | 1 | a0002c0003t0013g0239 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.964+8255T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43861123 | |||||||
| chr2:43861172 | T | C | 1 | a0002c0003t0098g0171 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.964+8304T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43861172 | |||||||
| chr2:43861176 | C | A | 1 | a0002c0003t0005g0257 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.964+8308C>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43861176 | |||||||
| chr2:43861179 | C | A | 6 | a0007c0009t0022g0005a0007c0009t0022g0032a0007c0009t0028g0033others(3): Show | 7 | HG01346.hp2 HG02486.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.964+8311C>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43861179 | |||||||
| chr2:43861251 | T | C | 5 | a0001c0001t0016g0003a0003c0010t0020g0036a0003c0010t0020g0037others(2): Show | 7 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(4): Show |
intron_variant | MODIFIER | c.964+8383T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43861251 | |||||||
| chr2:43861359 | T | G | 1 | a0003c0002t0092g0040 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.964+8491T>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43861359 | |||||||
| chr2:43861367 | T | G | 1 | a0011c0023t0084g0206 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.964+8499T>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43861367 | |||||||
| chr2:43861670 | C | T | 1 | a0003c0002t0008g0176 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.964+8802C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43861670 | |||||||
| chr2:43861684 | T | A | 1 | a0001c0001t0010g0082 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.964+8816T>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43861684 | |||||||
| chr2:43861712 | C | T | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+8844C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43861712 | |||||||
| chr2:43861739 | A | C | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+8871A>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43861739 | |||||||
| chr2:43861808 | C | T | 137 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(134): Show | 146 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(143): Show |
intron_variant | MODIFIER | c.964+8940C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43861808 | |||||||
| chr2:43861890 | A | G | 1 | a0004c0006t0085g0268 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.964+9022A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43861890 | |||||||
| chr2:43861909 | T | C | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+9041T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43861909 | |||||||
| chr2:43861942 | C | T | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+9074C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43861942 | |||||||
| chr2:43862086 | T | A | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+9218T>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43862086 | |||||||
| chr2:43862087 | G | A | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+9219G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43862087 | |||||||
| chr2:43862115 | G | T | 1 | a0006c0005t0004g0221 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.964+9247G>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43862115 | |||||||
| chr2:43862216 | A | C | 3 | a0003c0011t0012g0001a0003c0011t0012g0061a0003c0011t0091g0001 | 4 | HG02647.hp2 HG03130.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.964+9348A>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43862216 | |||||||
| chr2:43862216 | A | G | 138 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(135): Show | 147 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(144): Show |
intron_variant | MODIFIER | c.964+9348A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43862216 | |||||||
| chr2:43862294 | C | G | 1 | a0001c0001t0069g0129 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.964+9426C>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43862294 | |||||||
| chr2:43862333 | T | C | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+9465T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43862333 | |||||||
| chr2:43862358 | G | A | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+9490G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43862358 | |||||||
| chr2:43862360 | G | C | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+9492G>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43862360 | |||||||
| chr2:43862361 | T | A | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+9493T>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43862361 | |||||||
| chr2:43862376 | T | G | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+9508T>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43862376 | |||||||
| chr2:43862381 | T | TCTCTATA others(712): Show |
4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+9517_964+9518i others(721): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 43862381 | ||||||
| chr2:43862403 | T | G | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+9535T>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43862403 | |||||||
| chr2:43862408 | A | C | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+9540A>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43862408 | |||||||
| chr2:43862413 | G | T | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+9545G>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43862413 | |||||||
| chr2:43862420 | A | T | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+9552A>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43862420 | |||||||
| chr2:43862421 | T | A | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+9553T>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43862421 | |||||||
| chr2:43862426 | A | C | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-9550A>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43862426 | |||||||
| chr2:43862427 | A | T | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-9549A>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43862427 | |||||||
| chr2:43862431 | T | G | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-9545T>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43862431 | |||||||
| chr2:43862451 | A | AATAGAAT others(77): Show |
1 | a0002c0003t0090g0035 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.965-9514_965-9431d others(86): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 43862451 | ||||||
| chr2:43862462 | C | T | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-9514C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43862462 | |||||||
| chr2:43862468 | C | G | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-9508C>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43862468 | |||||||
| chr2:43862477 | A | G | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-9499A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43862477 | |||||||
| chr2:43862478 | T | C | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-9498T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43862478 | |||||||
| chr2:43862480 | C | A | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-9496C>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43862480 | |||||||
| chr2:43862546 | T | TCC | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-9430_965-9429i others(4): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43862546 | |||||||
| chr2:43862547 | A | G | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-9429A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43862547 | |||||||
| chr2:43862553 | A | G | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-9423A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43862553 | |||||||
| chr2:43862554 | A | G | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-9422A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43862554 | |||||||
| chr2:43862559 | A | C | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-9417A>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43862559 | |||||||
| chr2:43862560 | C | A | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-9416C>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43862560 | |||||||
| chr2:43862570 | G | C | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-9406G>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43862570 | |||||||
| chr2:43862579 | T | CAGAACTC others(2864): Show |
1 | a0003c0010t0110g0039 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.965-9398_965-9397i others(2873): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43862579 | |||||||
| chr2:43862579 | T | CAGAACTC others(2864): Show |
3 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038 | 3 | HG01192.hp1 HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.965-9398_965-9397i others(2873): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43862579 | |||||||
| chr2:43862587 | TTAC | T | 125 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(122): Show | 133 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(130): Show |
intron_variant | MODIFIER | c.965-9385_965-9383d others(5): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 43862587 | ||||||
| chr2:43862601 | C | A | 1 | a0006c0005t0002g0245 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.965-9375C>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43862601 | |||||||
| chr2:43862648 | C | T | 2 | a0003c0002t0042g0016a0003c0002t0093g0161 | 3 | HG01884.hp2 HG02809.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.965-9328C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43862648 | |||||||
| chr2:43862651 | T | C | 1 | a0003c0014t0079g0276 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.965-9325T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43862651 | |||||||
| chr2:43862652 | A | T | 1 | a0003c0014t0079g0276 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.965-9324A>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43862652 | |||||||
| chr2:43862676 | T | C | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-9300T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43862676 | |||||||
| chr2:43862711 | A | G | 2 | a0003c0002t0042g0016a0003c0002t0093g0161 | 3 | HG01884.hp2 HG02809.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.965-9265A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43862711 | |||||||
| chr2:43862789 | C | A | 152 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(149): Show | 164 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(161): Show |
intron_variant | MODIFIER | c.965-9187C>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43862789 | |||||||
| chr2:43862790 | T | G | 1 | a0001c0001t0001g0069 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.965-9186T>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43862790 | |||||||
| chr2:43862795 | G | A | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-9181G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43862795 | |||||||
| chr2:43862913 | T | C | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-9063T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43862913 | |||||||
| chr2:43863045 | G | A | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-8931G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43863045 | |||||||
| chr2:43863047 | G | A | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-8929G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43863047 | |||||||
| chr2:43863067 | C | T | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-8909C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43863067 | |||||||
| chr2:43863087 | A | G | 1 | a0003c0002t0004g0208 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.965-8889A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43863087 | |||||||
| chr2:43863131 | C | G | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-8845C>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43863131 | |||||||
| chr2:43863194 | T | C | 138 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(135): Show | 147 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(144): Show |
intron_variant | MODIFIER | c.965-8782T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43863194 | |||||||
| chr2:43863338 | T | C | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-8638T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43863338 | |||||||
| chr2:43863351 | C | T | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-8625C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43863351 | |||||||
| chr2:43863621 | A | G | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-8355A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43863621 | |||||||
| chr2:43863762 | C | G | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-8214C>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43863762 | |||||||
| chr2:43863798 | G | A | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-8178G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43863798 | |||||||
| chr2:43863857 | T | G | 1 | a0001c0001t0016g0003 | 3 | NA18970.hp2 NA19085.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.965-8119T>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43863857 | |||||||
| chr2:43863916 | G | A | 9 | a0003c0002t0002g0209a0003c0002t0019g0063a0003c0002t0019g0157others(6): Show | 9 | HG01109.hp2 HG01192.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.965-8060G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43863916 | |||||||
| chr2:43863919 | C | T | 137 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(134): Show | 146 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(143): Show |
intron_variant | MODIFIER | c.965-8057C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43863919 | |||||||
| chr2:43863944 | A | G | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-8032A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43863944 | |||||||
| chr2:43863958 | G | C | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-8018G>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43863958 | |||||||
| chr2:43863980 | A | G | 1 | a0013c0029t0066g0126 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.965-7996A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43863980 | |||||||
| chr2:43863990 | A | G | 1 | a0002c0003t0005g0229 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.965-7986A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43863990 | |||||||
| chr2:43864120 | T | C | 1 | a0008c0018t0002g0174 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.965-7856T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43864120 | |||||||
| chr2:43864140 | T | C | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-7836T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43864140 | |||||||
| chr2:43864228 | C | G | 12 | a0003c0002t0026g0041a0007c0009t0022g0005a0007c0009t0022g0032others(9): Show | 13 | HG01346.hp2 HG02109.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.965-7748C>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43864228 | |||||||
| chr2:43864281 | C | G | 141 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(138): Show | 150 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(147): Show |
intron_variant | MODIFIER | c.965-7695C>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43864281 | |||||||
| chr2:43864283 | T | C | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-7693T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43864283 | |||||||
| chr2:43864367 | T | C | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-7609T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43864367 | |||||||
| chr2:43864468 | A | G | 1 | a0003c0010t0020g0038 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.965-7508A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43864468 | |||||||
| chr2:43864490 | A | G | 7 | a0001c0001t0011g0011a0001c0001t0011g0012a0001c0001t0011g0123others(4): Show | 9 | HG01106.hp2 HG02451.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.965-7486A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43864490 | |||||||
| chr2:43864499 | A | G | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-7477A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43864499 | |||||||
| chr2:43864502 | C | A | 137 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(134): Show | 146 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(143): Show |
intron_variant | MODIFIER | c.965-7474C>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43864502 | |||||||
| chr2:43864646 | C | A | 3 | a0003c0011t0012g0001a0003c0011t0012g0061a0003c0011t0091g0001 | 4 | HG02647.hp2 HG03130.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.965-7330C>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43864646 | |||||||
| chr2:43864868 | A | ATAGGACT others(41): Show |
4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-7108_965-7107i others(50): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43864868 | |||||||
| chr2:43864869 | C | T | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-7107C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43864869 | |||||||
| chr2:43864921 | T | A | 3 | a0003c0011t0012g0001a0003c0011t0012g0061a0003c0011t0091g0001 | 4 | HG02647.hp2 HG03130.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.965-7055T>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43864921 | |||||||
| chr2:43864927 | C | T | 264 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(261): Show | 283 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(280): Show |
intron_variant | MODIFIER | c.965-7049C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43864927 | |||||||
| chr2:43864928 | A | G | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-7048A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43864928 | |||||||
| chr2:43865063 | T | C | 1 | a0001c0001t0001g0094 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.965-6913T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43865063 | |||||||
| chr2:43865106 | C | G | 137 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(134): Show | 146 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(143): Show |
intron_variant | MODIFIER | c.965-6870C>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43865106 | |||||||
| chr2:43865190 | C | T | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-6786C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43865190 | |||||||
| chr2:43865194 | CACTATCT others(161): Show |
C | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-6774_965-6607d others(2): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 43865194 | ||||||
| chr2:43865262 | A | G | 1 | a0007c0020t0061g0029 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.965-6714A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43865262 | |||||||
| chr2:43865267 | C | G | 189 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(186): Show | 205 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(202): Show |
intron_variant | MODIFIER | c.965-6709C>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43865267 | |||||||
| chr2:43865479 | C | A | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-6497C>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43865479 | |||||||
| chr2:43865487 | C | G | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-6489C>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43865487 | |||||||
| chr2:43865492 | T | C | 1 | a0002c0003t0098g0171 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.965-6484T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43865492 | |||||||
| chr2:43865555 | C | A | 138 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(135): Show | 147 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(144): Show |
intron_variant | MODIFIER | c.965-6421C>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43865555 | |||||||
| chr2:43865557 | C | T | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-6419C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43865557 | |||||||
| chr2:43865591 | C | A | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-6385C>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43865591 | |||||||
| chr2:43865592 | TCA | T | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-6382_965-6381d others(4): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 43865592 | ||||||
| chr2:43865599 | C | A | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-6377C>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43865599 | |||||||
| chr2:43865601 | A | T | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-6375A>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43865601 | |||||||
| chr2:43865614 | A | ACTCT | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-6360_965-6359i others(6): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 43865614 | ||||||
| chr2:43865634 | C | A | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-6342C>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43865634 | |||||||
| chr2:43865635 | C | T | 1 | a0001c0001t0062g0050 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.965-6341C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43865635 | |||||||
| chr2:43865636 | T | TG | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-6340_965-6339i others(3): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43865636 | |||||||
| chr2:43865637 | A | T | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-6339A>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43865637 | |||||||
| chr2:43865639 | T | TG | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-6336dupG | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 43865639 | ||||||
| chr2:43865653 | C | A | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-6323C>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43865653 | |||||||
| chr2:43865655 | C | A | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-6321C>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43865655 | |||||||
| chr2:43865659 | C | A | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-6317C>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43865659 | |||||||
| chr2:43865661 | C | G | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-6315C>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43865661 | |||||||
| chr2:43865671 | T | C | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-6305T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43865671 | |||||||
| chr2:43865679 | G | GTCTA | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-6294_965-6293i others(6): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 43865679 | ||||||
| chr2:43865691 | C | T | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-6285C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43865691 | |||||||
| chr2:43865696 | AATAT | A | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-6279_965-6276d others(6): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43865696 | |||||||
| chr2:43865702 | T | C | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-6274T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43865702 | |||||||
| chr2:43865703 | A | C | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-6273A>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43865703 | |||||||
| chr2:43865705 | G | C | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-6271G>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43865705 | |||||||
| chr2:43865712 | G | C | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-6264G>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43865712 | |||||||
| chr2:43865719 | C | T | 1 | a0002c0003t0005g0229 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.965-6257C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43865719 | |||||||
| chr2:43865723 | G | A | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-6253G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43865723 | |||||||
| chr2:43865820 | G | C | 138 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(135): Show | 147 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(144): Show |
intron_variant | MODIFIER | c.965-6156G>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43865820 | |||||||
| chr2:43865887 | C | T | 9 | a0001c0001t0003g0130a0001c0001t0011g0011a0001c0001t0011g0012others(6): Show | 11 | HG00733.hp1 HG01106.hp2 HG01934.hp1 others(8): Show |
intron_variant | MODIFIER | c.965-6089C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43865887 | |||||||
| chr2:43865899 | C | T | 2 | a0003c0002t0042g0016a0003c0002t0093g0161 | 3 | HG01884.hp2 HG02809.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.965-6077C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43865899 | |||||||
| chr2:43865912 | G | C | 1 | a0003c0002t0076g0238 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.965-6064G>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43865912 | |||||||
| chr2:43865923 | A | G | 5 | a0009c0012t0023g0026a0009c0012t0023g0027a0009c0012t0023g0028others(2): Show | 5 | HG02109.hp2 HG02559.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.965-6053A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43865923 | |||||||
| chr2:43865941 | C | G | 5 | a0002c0003t0002g0237a0002c0003t0013g0004a0002c0003t0013g0236others(2): Show | 7 | NA18948.hp1 NA18952.hp1 NA18954.hp2 others(4): Show |
intron_variant | MODIFIER | c.965-6035C>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43865941 | |||||||
| chr2:43865977 | G | C | 1 | a0006c0005t0041g0243 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.965-5999G>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43865977 | |||||||
| chr2:43866092 | G | A | 2 | a0002c0003t0002g0231a0002c0003t0105g0173 | 2 | HG01261.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.965-5884G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43866092 | |||||||
| chr2:43866137 | G | C | 84 | a0002c0003t0002g0019a0002c0003t0002g0044a0002c0003t0002g0045others(81): Show | 89 | HG00280.hp2 HG00323.hp1 HG00621.hp1 others(86): Show |
intron_variant | MODIFIER | c.965-5839G>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43866137 | |||||||
| chr2:43866210 | A | G | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-5766A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43866210 | |||||||
| chr2:43866211 | G | C | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-5765G>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43866211 | |||||||
| chr2:43866239 | G | A | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-5737G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43866239 | |||||||
| chr2:43866282 | CG | C | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-5691delG | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 43866282 | ||||||
| chr2:43866284 | G | A | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-5692G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43866284 | |||||||
| chr2:43866333 | A | G | 5 | a0003c0002t0021g0149a0003c0002t0021g0150a0003c0002t0021g0151others(2): Show | 6 | HG00642.hp2 HG01099.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.965-5643A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43866333 | |||||||
| chr2:43866352 | A | C | 1 | a0007c0020t0061g0029 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.965-5624A>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43866352 | |||||||
| chr2:43866395 | A | G | 1 | a0003c0022t0014g0261 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.965-5581A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43866395 | |||||||
| chr2:43866400 | G | A | 4 | a0001c0001t0033g0138a0001c0001t0070g0090a0001c0008t0015g0076others(1): Show | 4 | HG03490.hp2 HG03704.hp1 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.965-5576G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43866400 | |||||||
| chr2:43866482 | G | C | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-5494G>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43866482 | |||||||
| chr2:43866659 | C | T | 3 | a0007c0009t0022g0005a0007c0009t0022g0032a0007c0009t0049g0031 | 4 | HG01346.hp2 HG02486.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.965-5317C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43866659 | |||||||
| chr2:43866682 | G | A | 1 | a0002c0003t0005g0257 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.965-5294G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43866682 | |||||||
| chr2:43866730 | A | G | 1 | a0015c0028t0043g0291 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.965-5246A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43866730 | |||||||
| chr2:43866731 | C | T | 3 | a0002c0003t0012g0177a0002c0003t0101g0178a0002c0004t0008g0213 | 3 | HG01884.hp1 HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.965-5245C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43866731 | |||||||
| chr2:43866751 | T | C | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-5225T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43866751 | |||||||
| chr2:43866782 | A | G | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-5194A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43866782 | |||||||
| chr2:43866809 | C | T | 5 | a0003c0002t0002g0209a0003c0002t0019g0063a0003c0002t0019g0157others(2): Show | 5 | HG01109.hp2 HG02723.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.965-5167C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43866809 | |||||||
| chr2:43866819 | T | C | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-5157T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43866819 | |||||||
| chr2:43866824 | G | A | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-5152G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43866824 | |||||||
| chr2:43866879 | A | G | 1 | a0001c0001t0001g0116 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.965-5097A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43866879 | |||||||
| chr2:43866896 | C | T | 3 | a0003c0011t0012g0001a0003c0011t0012g0061a0003c0011t0091g0001 | 4 | HG02647.hp2 HG03130.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.965-5080C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43866896 | |||||||
| chr2:43866899 | A | G | 2 | a0002c0003t0005g0196a0002c0003t0005g0230 | 2 | NA18942.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.965-5077A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43866899 | |||||||
| chr2:43866926 | G | A | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-5050G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43866926 | |||||||
| chr2:43866951 | G | A | 1 | a0018c0027t0005g0232 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.965-5025G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43866951 | |||||||
| chr2:43867001 | G | A | 1 | a0006c0005t0041g0243 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.965-4975G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43867001 | |||||||
| chr2:43867015 | C | T | 12 | a0001c0001t0007g0142a0001c0008t0008g0274a0001c0008t0015g0144others(9): Show | 13 | HG00280.hp1 HG00735.hp2 HG01069.hp1 others(10): Show |
intron_variant | MODIFIER | c.965-4961C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43867015 | |||||||
| chr2:43867017 | T | C | 1 | a0009c0012t0072g0024 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.965-4959T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43867017 | |||||||
| chr2:43867026 | G | A | 5 | a0003c0002t0019g0165a0003c0010t0020g0036a0003c0010t0020g0037others(2): Show | 5 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.965-4950G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43867026 | |||||||
| chr2:43867175 | G | A | 6 | a0001c0001t0035g0053a0001c0001t0035g0054a0003c0002t0021g0149others(3): Show | 7 | HG00642.hp2 HG01099.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.965-4801G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43867175 | |||||||
| chr2:43867207 | G | A | 2 | a0003c0002t0002g0175a0003c0002t0102g0207 | 2 | HG00639.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.965-4769G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43867207 | |||||||
| chr2:43867208 | A | G | 1 | a0001c0001t0003g0154 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.965-4768A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43867208 | |||||||
| chr2:43867216 | G | A | 1 | a0003c0002t0089g0191 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.965-4760G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43867216 | |||||||
| chr2:43867226 | T | A | 1 | a0002c0003t0004g0222 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.965-4750T>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43867226 | |||||||
| chr2:43867260 | C | T | 1 | a0003c0010t0110g0039 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.965-4716C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43867260 | |||||||
| chr2:43867347 | T | TA | 181 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(178): Show | 196 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(193): Show |
intron_variant | MODIFIER | c.965-4617dupA | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 43867347 | ||||||
| chr2:43867477 | A | G | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-4499A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43867477 | |||||||
| chr2:43867513 | A | G | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-4463A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43867513 | |||||||
| chr2:43867547 | C | G | 1 | a0004c0006t0025g0277 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.965-4429C>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43867547 | |||||||
| chr2:43867560 | C | T | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-4416C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43867560 | |||||||
| chr2:43867582 | G | A | 1 | a0003c0014t0043g0217 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.965-4394G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43867582 | |||||||
| chr2:43867601 | G | T | 1 | a0003c0002t0026g0041 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.965-4375G>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43867601 | |||||||
| chr2:43867619 | C | T | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-4357C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43867619 | |||||||
| chr2:43867706 | G | A | 21 | a0003c0002t0001g0021a0003c0002t0001g0189a0003c0002t0001g0214others(18): Show | 23 | HG00438.hp1 HG00741.hp2 HG01978.hp2 others(20): Show |
intron_variant | MODIFIER | c.965-4270G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43867706 | |||||||
| chr2:43867843 | C | T | 2 | a0001c0001t0003g0051a0001c0001t0032g0081 | 2 | NA18942.hp2 NA18954.hp1 |
intron_variant | MODIFIER | c.965-4133C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43867843 | |||||||
| chr2:43867875 | A | G | 1 | a0001c0001t0003g0114 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.965-4101A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43867875 | |||||||
| chr2:43867884 | T | C | 1 | a0004c0006t0024g0043 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.965-4092T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43867884 | |||||||
| chr2:43867914 | G | T | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-4062G>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43867914 | |||||||
| chr2:43867938 | T | C | 3 | a0001c0001t0003g0154a0001c0001t0030g0117a0001c0001t0030g0119 | 3 | HG00597.hp1 HG02027.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.965-4038T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43867938 | |||||||
| chr2:43868069 | C | G | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-3907C>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43868069 | |||||||
| chr2:43868074 | T | G | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-3902T>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43868074 | |||||||
| chr2:43868091 | A | G | 2 | a0003c0002t0004g0172a0003c0022t0014g0261 | 2 | HG02818.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.965-3885A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43868091 | |||||||
| chr2:43868101 | C | T | 2 | a0001c0001t0001g0094a0003c0002t0026g0041 | 2 | NA18957.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.965-3875C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43868101 | |||||||
| chr2:43868187 | G | C | 142 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(139): Show | 151 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(148): Show |
intron_variant | MODIFIER | c.965-3789G>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43868187 | |||||||
| chr2:43868193 | A | G | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-3783A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43868193 | |||||||
| chr2:43868227 | A | C | 139 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(136): Show | 148 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(145): Show |
intron_variant | MODIFIER | c.965-3749A>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43868227 | |||||||
| chr2:43868337 | G | A | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-3639G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43868337 | |||||||
| chr2:43868347 | T | C | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-3629T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43868347 | |||||||
| chr2:43868426 | G | A | 2 | a0003c0002t0042g0016a0003c0002t0093g0161 | 3 | HG01884.hp2 HG02809.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.965-3550G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43868426 | |||||||
| chr2:43868446 | C | T | 1 | a0006c0005t0088g0246 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.965-3530C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43868446 | |||||||
| chr2:43868482 | A | G | 139 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(136): Show | 148 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(145): Show |
intron_variant | MODIFIER | c.965-3494A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43868482 | |||||||
| chr2:43868492 | T | TTATCTGT others(37): Show |
1 | a0015c0028t0043g0291 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.965-3462_965-3419d others(46): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 43868492 | ||||||
| chr2:43868533 | T | C | 3 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038 | 3 | HG01192.hp1 HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.965-3443T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43868533 | |||||||
| chr2:43868558 | G | C | 142 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(139): Show | 151 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(148): Show |
intron_variant | MODIFIER | c.965-3418G>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43868558 | |||||||
| chr2:43868611 | G | A | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-3365G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43868611 | |||||||
| chr2:43868725 | C | T | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-3251C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43868725 | |||||||
| chr2:43868765 | A | G | 3 | a0003c0011t0012g0001a0003c0011t0012g0061a0003c0011t0091g0001 | 4 | HG02647.hp2 HG03130.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.965-3211A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43868765 | |||||||
| chr2:43868824 | G | A | 142 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(139): Show | 151 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(148): Show |
intron_variant | MODIFIER | c.965-3152G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43868824 | |||||||
| chr2:43868871 | T | A | 138 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(135): Show | 147 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(144): Show |
intron_variant | MODIFIER | c.965-3105T>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43868871 | |||||||
| chr2:43868897 | C | G | 11 | a0007c0009t0022g0005a0007c0009t0022g0032a0007c0009t0028g0033others(8): Show | 12 | HG01346.hp2 HG02109.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.965-3079C>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43868897 | |||||||
| chr2:43868915 | C | A | 4 | a0003c0002t0095g0242a0003c0002t0104g0216a0003c0014t0043g0217others(1): Show | 4 | HG02717.hp1 HG02717.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-3061C>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43868915 | |||||||
| chr2:43868919 | C | G | 1 | a0006c0005t0004g0023 | 2 | HG02132.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.965-3057C>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43868919 | |||||||
| chr2:43868999 | C | T | 1 | a0002c0003t0013g0004 | 3 | NA18974.hp1 NA18998.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.965-2977C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43868999 | |||||||
| chr2:43869000 | G | A | 259 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(256): Show | 276 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(273): Show |
intron_variant | MODIFIER | c.965-2976G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43869000 | |||||||
| chr2:43869120 | T | G | 261 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(258): Show | 279 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(276): Show |
intron_variant | MODIFIER | c.965-2856T>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43869120 | |||||||
| chr2:43869179 | G | A | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-2797G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43869179 | |||||||
| chr2:43869194 | T | C | 1 | a0001c0001t0001g0105 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.965-2782T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43869194 | |||||||
| chr2:43869197 | T | A | 261 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(258): Show | 279 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(276): Show |
intron_variant | MODIFIER | c.965-2779T>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43869197 | |||||||
| chr2:43869259 | G | A | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-2717G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43869259 | |||||||
| chr2:43869263 | G | A | 269 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(266): Show | 289 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(286): Show |
intron_variant | MODIFIER | c.965-2713G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43869263 | |||||||
| chr2:43869318 | A | C | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-2658A>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43869318 | |||||||
| chr2:43869420 | T | A | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-2556T>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43869420 | |||||||
| chr2:43869631 | T | A | 264 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(261): Show | 283 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(280): Show |
intron_variant | MODIFIER | c.965-2345T>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43869631 | |||||||
| chr2:43869643 | C | A | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-2333C>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43869643 | |||||||
| chr2:43869669 | A | G | 1 | a0002c0003t0002g0197 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.965-2307A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43869669 | |||||||
| chr2:43869975 | A | C | 3 | a0003c0002t0004g0267a0003c0002t0039g0279a0004c0006t0083g0062 | 3 | HG00733.hp2 HG01175.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.965-2001A>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43869975 | |||||||
| chr2:43869975 | A | G | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-2001A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43869975 | |||||||
| chr2:43870131 | G | T | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-1845G>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43870131 | |||||||
| chr2:43870189 | C | T | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-1787C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43870189 | |||||||
| chr2:43870208 | TCTCACTG others(13): Show |
T | 3 | a0002c0003t0012g0177a0002c0003t0101g0178a0002c0004t0008g0213 | 3 | HG01884.hp1 HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.965-1761_965-1742d others(22): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 43870208 | ||||||
| chr2:43870221 | A | G | 76 | a0002c0003t0002g0019a0002c0003t0002g0044a0002c0003t0002g0045others(73): Show | 80 | HG00280.hp2 HG00323.hp1 HG00621.hp1 others(77): Show |
intron_variant | MODIFIER | c.965-1755A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43870221 | |||||||
| chr2:43870228 | C | T | 258 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(255): Show | 276 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(273): Show |
intron_variant | MODIFIER | c.965-1748C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43870228 | |||||||
| chr2:43870249 | A | C | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-1727A>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43870249 | |||||||
| chr2:43870293 | C | CAATT | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-1683_965-1682i others(6): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43870293 | |||||||
| chr2:43870398 | G | T | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-1578G>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43870398 | |||||||
| chr2:43870503 | C | A | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-1473C>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43870503 | |||||||
| chr2:43870529 | T | C | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-1447T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43870529 | |||||||
| chr2:43870543 | C | T | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-1433C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43870543 | |||||||
| chr2:43870560 | G | C | 8 | a0001c0001t0001g0070a0001c0001t0001g0072a0001c0001t0001g0080others(5): Show | 8 | HG01081.hp2 HG02080.hp1 HG02165.hp2 others(5): Show |
intron_variant | MODIFIER | c.965-1416G>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43870560 | |||||||
| chr2:43870571 | G | A | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-1405G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43870571 | |||||||
| chr2:43870573 | C | T | 9 | a0002c0003t0004g0248a0002c0003t0005g0195a0002c0003t0005g0201others(6): Show | 9 | HG01106.hp1 HG01928.hp1 HG01943.hp2 others(6): Show |
intron_variant | MODIFIER | c.965-1403C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43870573 | |||||||
| chr2:43870574 | G | T | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-1402G>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43870574 | |||||||
| chr2:43870640 | G | T | 1 | a0003c0010t0110g0039 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.965-1336G>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43870640 | |||||||
| chr2:43870691 | G | A | 1 | a0003c0002t0027g0280 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.965-1285G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43870691 | |||||||
| chr2:43870755 | C | T | 1 | a0002c0004t0009g0042 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.965-1221C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43870755 | |||||||
| chr2:43870798 | C | CACCATCT others(12): Show |
2 | a0003c0021t0007g0030a0006c0005t0002g0260 | 2 | HG00741.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.965-1176_965-1175i others(21): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 43870798 | ||||||
| chr2:43870875 | A | G | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-1101A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43870875 | |||||||
| chr2:43870877 | T | A | 2 | a0003c0002t0042g0016a0003c0002t0093g0161 | 3 | HG01884.hp2 HG02809.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.965-1099T>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43870877 | |||||||
| chr2:43870890 | G | A | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-1086G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43870890 | |||||||
| chr2:43871016 | C | T | 3 | a0002c0003t0012g0177a0002c0003t0101g0178a0002c0004t0008g0213 | 3 | HG01884.hp1 HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.965-960C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43871016 | |||||||
| chr2:43871020 | G | GGATAGAA others(75): Show |
4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-921_965-920ins others(82): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 43871020 | ||||||
| chr2:43871120 | C | G | 4 | a0001c0001t0007g0142a0001c0008t0015g0144a0001c0008t0051g0141others(1): Show | 4 | HG01123.hp2 HG01167.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.965-856C>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43871120 | |||||||
| chr2:43871129 | T | C | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-847T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43871129 | |||||||
| chr2:43871140 | C | T | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-836C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43871140 | |||||||
| chr2:43871162 | ATCTATCT others(257): Show |
A | 3 | a0002c0004t0009g0185a0002c0004t0009g0188a0002c0004t0009g0225 | 3 | HG01433.hp1 HG01496.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.965-773_965-510del | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 43871162 | ||||||
| chr2:43871192 | A | G | 117 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(114): Show | 123 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(120): Show |
intron_variant | MODIFIER | c.965-784A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43871192 | |||||||
| chr2:43871195 | G | A | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-781G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43871195 | |||||||
| chr2:43871282 | C | T | 1 | a0003c0002t0106g0162 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.965-694C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43871282 | |||||||
| chr2:43871286 | A | C | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-690A>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43871286 | |||||||
| chr2:43871308 | C | G | 26 | a0002c0003t0002g0044a0002c0003t0002g0045a0002c0003t0002g0200others(23): Show | 28 | HG00280.hp2 HG01070.hp1 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.965-668C>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43871308 | |||||||
| chr2:43871374 | A | AGAACTCT others(447): Show |
1 | a0003c0010t0020g0038 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.965-587_965-586ins others(454): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 43871374 | ||||||
| chr2:43871374 | A | AGAACTCT others(447): Show |
3 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0110g0039 | 3 | HG02895.hp2 HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.965-587_965-586ins others(454): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 43871374 | ||||||
| chr2:43871426 | G | A | 146 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(143): Show | 156 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(153): Show |
intron_variant | MODIFIER | c.965-550G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43871426 | |||||||
| chr2:43871457 | T | C | 1 | a0003c0002t0021g0150 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.965-519T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43871457 | |||||||
| chr2:43871467 | G | A | 127 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(124): Show | 135 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(132): Show |
intron_variant | MODIFIER | c.965-509G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43871467 | |||||||
| chr2:43871490 | C | G | 11 | a0003c0002t0002g0209a0003c0002t0018g0015a0003c0002t0018g0158others(8): Show | 12 | HG01074.hp1 HG01099.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.965-486C>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43871490 | |||||||
| chr2:43871542 | C | T | 3 | a0002c0003t0005g0233a0002c0003t0005g0249a0003c0002t0076g0238 | 3 | NA18964.hp2 NA19005.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.965-434C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43871542 | |||||||
| chr2:43871645 | G | A | 4 | a0003c0002t0021g0149a0003c0002t0021g0150a0003c0002t0021g0151others(1): Show | 5 | HG00642.hp2 HG01099.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.965-331G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43871645 | |||||||
| chr2:43871687 | G | T | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-289G>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43871687 | |||||||
| chr2:43871716 | T | C | 142 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(139): Show | 152 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(149): Show |
intron_variant | MODIFIER | c.965-260T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43871716 | |||||||
| chr2:43871902 | G | A | 3 | a0002c0003t0012g0177a0002c0003t0101g0178a0002c0004t0008g0213 | 3 | HG01884.hp1 HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.965-74G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43871902 | |||||||
| chr2:43871917 | C | T | 1 | a0003c0002t0021g0150 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.965-59C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43871917 | |||||||
| chr2:43871918 | A | G | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-58A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 6/12 | chr2 | 43871918 | |||||||
| chr2:43872191 | C | T | 3 | a0003c0011t0012g0001a0003c0011t0012g0061a0003c0011t0091g0001 | 4 | HG02647.hp2 HG03130.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.1128-32C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 7/12 | chr2 | 43872191 | |||||||
| chr2:43872348 | C | G | 3 | a0003c0011t0012g0001a0003c0011t0012g0061a0003c0011t0091g0001 | 4 | HG02647.hp2 HG03130.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.1211+42C>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 8/12 | chr2 | 43872348 | |||||||
| chr2:43872406 | G | A | 1 | a0011c0023t0084g0206 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1211+100G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 8/12 | chr2 | 43872406 | |||||||
| chr2:43872443 | G | A | 84 | a0002c0003t0002g0019a0002c0003t0002g0044a0002c0003t0002g0045others(81): Show | 89 | HG00280.hp2 HG00323.hp1 HG00621.hp1 others(86): Show |
intron_variant | MODIFIER | c.1211+137G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 8/12 | chr2 | 43872443 | |||||||
| chr2:43872454 | G | C | 1 | a0002c0003t0090g0035 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1211+148G>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 8/12 | chr2 | 43872454 | |||||||
| chr2:43872495 | G | A | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.1211+189G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 8/12 | chr2 | 43872495 | |||||||
| chr2:43872652 | A | G | 1 | a0001c0001t0001g0096 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1211+346A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 8/12 | chr2 | 43872652 | |||||||
| chr2:43872687 | C | G | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.1211+381C>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 8/12 | chr2 | 43872687 | |||||||
| chr2:43872754 | C | T | 1 | a0002c0003t0005g0204 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1211+448C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 8/12 | chr2 | 43872754 | |||||||
| chr2:43872876 | T | A | 25 | a0002c0003t0002g0044a0002c0003t0002g0045a0002c0003t0002g0200others(22): Show | 27 | HG00280.hp2 HG01070.hp1 HG01106.hp1 others(24): Show |
intron_variant | MODIFIER | c.1211+570T>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 8/12 | chr2 | 43872876 | |||||||
| chr2:43872924 | C | T | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.1211+618C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 8/12 | chr2 | 43872924 | |||||||
| chr2:43872938 | G | A | 128 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(125): Show | 136 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(133): Show |
intron_variant | MODIFIER | c.1211+632G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 8/12 | chr2 | 43872938 | |||||||
| chr2:43872965 | TAC | T | 4 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.1211+665_1211+666d others(4): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 43872965 | ||||||
| chr2:43872981 | C | T | 1 | a0013c0029t0066g0126 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1211+675C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 8/12 | chr2 | 43872981 | |||||||
| chr2:43873030 | C | G | 142 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(139): Show | 151 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(148): Show |
intron_variant | MODIFIER | c.1211+724C>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 8/12 | chr2 | 43873030 | |||||||
| chr2:43873189 | A | AT | 22 | a0002c0003t0012g0147a0002c0003t0039g0170a0002c0003t0090g0035others(19): Show | 23 | HG00738.hp2 HG01891.hp2 HG01978.hp2 others(20): Show |
intron_variant | MODIFIER | c.1212-581dupT | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 43873189 | ||||||
| chr2:43873189 | A | ATT | 15 | a0002c0003t0004g0222a0002c0003t0004g0223a0002c0003t0005g0229others(12): Show | 16 | HG01256.hp1 HG01433.hp1 HG01496.hp2 others(13): Show |
intron_variant | MODIFIER | c.1212-582_1212-581d others(4): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 43873189 | ||||||
| chr2:43873189 | AT | A | 16 | a0001c0001t0003g0114a0001c0001t0003g0122a0001c0001t0011g0123others(13): Show | 17 | HG00735.hp1 HG01109.hp2 HG01167.hp2 others(14): Show |
intron_variant | MODIFIER | c.1212-581delT | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 43873189 | ||||||
| chr2:43873218 | T | C | 141 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(138): Show | 151 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(148): Show |
intron_variant | MODIFIER | c.1212-569T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 8/12 | chr2 | 43873218 | |||||||
| chr2:43873244 | A | G | 3 | a0001c0001t0001g0048a0001c0001t0001g0088a0001c0001t0060g0049 | 3 | NA18959.hp2 NA18986.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.1212-543A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 8/12 | chr2 | 43873244 | |||||||
| chr2:43873457 | G | T | 5 | a0009c0012t0023g0026a0009c0012t0023g0027a0009c0012t0023g0028others(2): Show | 5 | HG02109.hp2 HG02559.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1212-330G>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 8/12 | chr2 | 43873457 | |||||||
| chr2:43873472 | G | A | 2 | a0001c0001t0003g0075a0001c0001t0003g0154 | 2 | NA18981.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.1212-315G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 8/12 | chr2 | 43873472 | |||||||
| chr2:43873488 | A | G | 1 | a0002c0003t0097g0256 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1212-299A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 8/12 | chr2 | 43873488 | |||||||
| chr2:43873497 | G | A | 1 | a0002c0003t0103g0194 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1212-290G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 8/12 | chr2 | 43873497 | |||||||
| chr2:43873542 | T | C | 2 | a0001c0001t0001g0070a0001c0001t0001g0072 | 2 | HG01081.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.1212-245T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 8/12 | chr2 | 43873542 | |||||||
| chr2:43873563 | G | C | 1 | a0003c0002t0092g0040 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1212-224G>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 8/12 | chr2 | 43873563 | |||||||
| chr2:43873601 | A | G | 1 | a0002c0003t0103g0194 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1212-186A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 8/12 | chr2 | 43873601 | |||||||
| chr2:43873620 | C | G | 5 | a0003c0002t0021g0149a0003c0002t0021g0150a0003c0002t0021g0151others(2): Show | 6 | HG00642.hp2 HG01099.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1212-167C>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 8/12 | chr2 | 43873620 | |||||||
| chr2:43873666 | A | C | 1 | a0001c0001t0001g0094 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1212-121A>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 8/12 | chr2 | 43873666 | |||||||
| chr2:43873710 | T | C | 28 | a0002c0003t0002g0234a0002c0003t0002g0255a0002c0004t0009g0251others(25): Show | 31 | HG00438.hp1 HG00741.hp2 HG01192.hp1 others(28): Show |
intron_variant | MODIFIER | c.1212-77T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 8/12 | chr2 | 43873710 | |||||||
| chr2:43873732 | G | A | 26 | a0003c0002t0001g0021a0003c0002t0001g0189a0003c0002t0001g0214others(23): Show | 29 | HG00438.hp1 HG00741.hp2 HG01192.hp1 others(26): Show |
intron_variant | MODIFIER | c.1212-55G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 8/12 | chr2 | 43873732 | |||||||
| chr2:43874011 | C | T | 1 | a0006c0005t0004g0023 | 2 | HG02132.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.1411+25C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 9/12 | chr2 | 43874011 | |||||||
| chr2:43874075 | CA | C | 277 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(274): Show | 297 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(294): Show |
intron_variant | MODIFIER | c.1411+90delA | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 9/12 | chr2 | 43874075 | |||||||
| chr2:43874090 | A | G | 35 | a0001c0008t0015g0144a0001c0008t0029g0152a0001c0008t0050g0073others(32): Show | 36 | HG00738.hp2 HG01070.hp2 HG01071.hp2 others(33): Show |
intron_variant | MODIFIER | c.1411+104A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 9/12 | chr2 | 43874090 | |||||||
| chr2:43874155 | C | T | 2 | a0003c0002t0004g0266a0003c0002t0004g0278 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1411+169C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 9/12 | chr2 | 43874155 | |||||||
| chr2:43874233 | A | G | 8 | a0002c0003t0101g0178a0003c0002t0104g0216a0003c0014t0043g0217others(5): Show | 9 | HG01884.hp1 HG02717.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.1412-174A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 9/12 | chr2 | 43874233 | |||||||
| chr2:43874255 | A | G | 240 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(237): Show | 255 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.1412-152A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 9/12 | chr2 | 43874255 | |||||||
| chr2:43874291 | T | A | 2 | a0003c0002t0095g0242a0003c0010t0110g0039 | 2 | HG02886.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.1412-116T>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 9/12 | chr2 | 43874291 | |||||||
| chr2:43874291 | T | G | 145 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(142): Show | 154 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(151): Show |
intron_variant | MODIFIER | c.1412-116T>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 9/12 | chr2 | 43874291 | |||||||
| chr2:43874398 | A | AT | 66 | a0001c0001t0001g0009a0001c0001t0001g0080a0001c0001t0001g0100others(63): Show | 73 | HG00099.hp2 HG00438.hp2 HG00597.hp1 others(70): Show |
splice_region_variant&intron_variant | LOW | c.1412-9_1412-8insT | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 9/12 | chr2 | 43874398 | |||||||
| chr2:43874399 | C | T | 243 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(240): Show | 260 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(257): Show |
splice_region_variant&intron_variant | LOW | c.1412-8C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 9/12 | chr2 | 43874399 | |||||||
| chr2:43874510 | G | GC | 84 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0070others(81): Show | 90 | HG00280.hp2 HG00323.hp1 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.1488+33dupC | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 43874510 | ||||||
| chr2:43874510 | G | GCC | 89 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0069others(86): Show | 96 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.1488+32_1488+33dup others(2): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 43874510 | ||||||
| chr2:43874510 | G | GCCC | 37 | a0001c0001t0001g0008a0001c0001t0001g0085a0001c0001t0001g0088others(34): Show | 38 | HG00099.hp1 HG00280.hp1 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.1488+31_1488+33dup others(3): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 43874510 | ||||||
| chr2:43874528 | T | C | 1 | a0002c0003t0098g0171 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1488+45T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 10/12 | chr2 | 43874528 | |||||||
| chr2:43874529 | G | A | 7 | a0001c0001t0001g0009a0001c0001t0001g0100a0001c0001t0001g0105others(4): Show | 8 | HG00639.hp1 HG01928.hp2 HG01934.hp2 others(5): Show |
intron_variant | MODIFIER | c.1488+46G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 10/12 | chr2 | 43874529 | |||||||
| chr2:43874572 | T | C | 44 | a0001c0001t0001g0047a0001c0001t0058g0110a0001c0001t0069g0129others(41): Show | 46 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(43): Show |
intron_variant | MODIFIER | c.1488+89T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 10/12 | chr2 | 43874572 | |||||||
| chr2:43874604 | C | T | 3 | a0002c0003t0002g0231a0002c0003t0105g0173a0013c0029t0066g0126 | 3 | HG01261.hp1 HG02602.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1488+121C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 10/12 | chr2 | 43874604 | |||||||
| chr2:43874688 | G | A | 217 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(214): Show | 231 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(228): Show |
intron_variant | MODIFIER | c.1488+205G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 10/12 | chr2 | 43874688 | |||||||
| chr2:43874726 | T | TA | 6 | a0003c0002t0042g0016a0003c0002t0093g0161a0003c0002t0095g0242others(3): Show | 7 | HG01884.hp2 HG02647.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1488+251dupA | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 43874726 | ||||||
| chr2:43874745 | T | C | 19 | a0001c0001t0029g0046a0002c0003t0012g0147a0002c0003t0039g0170others(16): Show | 21 | HG00738.hp2 HG01346.hp2 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.1488+262T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 10/12 | chr2 | 43874745 | |||||||
| chr2:43874804 | C | G | 1 | a0002c0003t0004g0222 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1488+321C>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 10/12 | chr2 | 43874804 | |||||||
| chr2:43874825 | G | A | 18 | a0001c0001t0010g0082a0001c0008t0015g0074a0001c0008t0015g0144others(15): Show | 19 | HG01069.hp2 HG01192.hp2 HG01256.hp1 others(16): Show |
intron_variant | MODIFIER | c.1489-321G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 10/12 | chr2 | 43874825 | |||||||
| chr2:43874900 | G | A | 4 | a0007c0009t0022g0005a0007c0009t0022g0032a0007c0009t0028g0033others(1): Show | 5 | HG02486.hp1 HG02630.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1489-246G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 10/12 | chr2 | 43874900 | |||||||
| chr2:43874911 | C | T | 3 | a0003c0010t0020g0036a0003c0010t0020g0037a0003c0010t0020g0038 | 3 | HG01192.hp1 HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1489-235C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 10/12 | chr2 | 43874911 | |||||||
| chr2:43875027 | C | T | 3 | a0001c0001t0001g0002a0001c0001t0001g0047a0001c0001t0001g0069 | 5 | HG00558.hp2 NA18939.hp1 NA18944.hp1 others(2): Show |
intron_variant | MODIFIER | c.1489-119C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 10/12 | chr2 | 43875027 | |||||||
| chr2:43875058 | T | C | 12 | a0001c0001t0048g0086a0001c0001t0070g0090a0002c0003t0020g0252others(9): Show | 13 | HG00280.hp2 HG01192.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.1489-88T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 10/12 | chr2 | 43875058 | |||||||
| chr2:43875085 | G | A | 1 | a0002c0003t0013g0239 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1489-61G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 10/12 | chr2 | 43875085 | |||||||
| chr2:43875096 | T | C | 99 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(96): Show | 108 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(105): Show |
intron_variant | MODIFIER | c.1489-50T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 10/12 | chr2 | 43875096 | |||||||
| chr2:43875114 | C | T | 2 | a0003c0002t0042g0016a0003c0002t0093g0161 | 3 | HG01884.hp2 HG02809.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1489-32C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 10/12 | chr2 | 43875114 | |||||||
| chr2:43875428 | C | T | 3 | a0009c0012t0023g0026a0009c0012t0023g0027a0009c0012t0023g0028 | 3 | HG02109.hp2 HG03209.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1756+15C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 11/12 | chr2 | 43875428 | |||||||
| chr2:43875435 | T | C | 8 | a0001c0001t0059g0133a0002c0003t0012g0147a0002c0003t0012g0177others(5): Show | 10 | HG02647.hp2 HG02965.hp1 HG02976.hp2 others(7): Show |
intron_variant | MODIFIER | c.1756+22T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 11/12 | chr2 | 43875435 | |||||||
| chr2:43875495 | C | T | 97 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(94): Show | 106 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(103): Show |
intron_variant | MODIFIER | c.1756+82C>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 11/12 | chr2 | 43875495 | |||||||
| chr2:43875520 | G | T | 1 | a0001c0001t0003g0104 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1756+107G>T | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 11/12 | chr2 | 43875520 | |||||||
| chr2:43875522 | C | A | 1 | a0014c0025t0074g0156 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1756+109C>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 11/12 | chr2 | 43875522 | |||||||
| chr2:43875814 | G | C | 1 | a0003c0022t0014g0261 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1756+401G>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 11/12 | chr2 | 43875814 | |||||||
| chr2:43875878 | T | C | 272 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(269): Show | 291 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(288): Show |
intron_variant | MODIFIER | c.1756+465T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 11/12 | chr2 | 43875878 | |||||||
| chr2:43876098 | T | C | 76 | a0001c0001t0001g0140a0001c0001t0003g0051a0001c0001t0003g0058others(73): Show | 81 | HG00280.hp2 HG00438.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.1756+685T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 11/12 | chr2 | 43876098 | |||||||
| chr2:43876221 | G | A | 1 | a0012c0031t0045g0025 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1756+808G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 11/12 | chr2 | 43876221 | |||||||
| chr2:43876289 | C | G | 1 | a0001c0001t0003g0103 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1756+876C>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 11/12 | chr2 | 43876289 | |||||||
| chr2:43876419 | A | G | 2 | a0008c0016t0044g0192a0008c0016t0044g0193 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1756+1006A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 11/12 | chr2 | 43876419 | |||||||
| chr2:43876422 | G | A | 1 | a0002c0003t0090g0035 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1756+1009G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 11/12 | chr2 | 43876422 | |||||||
| chr2:43876482 | A | G | 3 | a0002c0004t0037g0228a0002c0004t0038g0020a0002c0004t0081g0227 | 4 | NA18944.hp2 NA18959.hp1 NA18969.hp2 others(1): Show |
intron_variant | MODIFIER | c.1756+1069A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 11/12 | chr2 | 43876482 | |||||||
| chr2:43876618 | TGTGAGAA others(12): Show |
T | 2 | a0003c0014t0043g0217a0015c0028t0043g0291 | 2 | HG02717.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1757-924_1757-906d others(21): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr2 | 43876618 | ||||||
| chr2:43876867 | T | C | 1 | a0001c0001t0007g0145 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1757-694T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 11/12 | chr2 | 43876867 | |||||||
| chr2:43876873 | G | A | 1 | a0014c0025t0074g0156 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1757-688G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 11/12 | chr2 | 43876873 | |||||||
| chr2:43876890 | G | A | 5 | a0001c0001t0070g0090a0002c0003t0020g0252a0003c0010t0020g0036others(2): Show | 5 | HG00280.hp2 HG01192.hp1 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.1757-671G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 11/12 | chr2 | 43876890 | |||||||
| chr2:43876928 | G | A | 5 | a0001c0001t0070g0090a0002c0003t0020g0252a0003c0010t0020g0036others(2): Show | 5 | HG00280.hp2 HG01192.hp1 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.1757-633G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 11/12 | chr2 | 43876928 | |||||||
| chr2:43877016 | A | G | 79 | a0001c0001t0007g0057a0001c0001t0007g0095a0001c0001t0007g0142others(76): Show | 84 | HG00099.hp2 HG00280.hp2 HG00639.hp2 others(81): Show |
intron_variant | MODIFIER | c.1757-545A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 11/12 | chr2 | 43877016 | |||||||
| chr2:43877062 | A | G | 235 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(232): Show | 253 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(250): Show |
intron_variant | MODIFIER | c.1757-499A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 11/12 | chr2 | 43877062 | |||||||
| chr2:43877172 | A | G | 6 | a0001c0001t0070g0090a0002c0003t0020g0252a0003c0002t0095g0242others(3): Show | 6 | HG00280.hp2 HG01192.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1757-389A>G | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 11/12 | chr2 | 43877172 | |||||||
| chr2:43877456 | T | C | 1 | a0002c0003t0096g0184 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1757-105T>C | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 11/12 | chr2 | 43877456 | |||||||
| chr2:43877471 | ACT | A | 49 | a0001c0001t0001g0048a0001c0001t0001g0085a0001c0001t0007g0057others(46): Show | 51 | HG00099.hp2 HG00639.hp2 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.1757-87_1757-86del others(2): Show |
ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr2 | 43877471 | ||||||
| chr2:43877689 | G | A | 2 | a0005c0007t0006g0055a0005c0007t0006g0127 | 2 | HG01168.hp1 HG01169.hp1 |
splice_donor_variant&intron_variant | HIGH | c.1884+1G>A | ABCG8 | ENSG00000143921.9 | transcript | ENST00000272286.4 | protein_coding | 12/12 | chr2 | 43877689 |