Search by Gene
| Item | Value |
|---|---|
| geneid | 64240 |
| ensemblid | ENSG00000138075.14 |
| hgncid | 13886 |
| symbol | ABCG5 |
| name | ATP binding cassette subfamily G member 5 |
| refseq_nuc | NM_022436.3 |
| refseq_prot | NP_071881.1 |
| ensembl_nuc | ENST00000405322.8 |
| ensembl_prot | ENSP00000384513.2 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 43812472 |
| end | 43838839 |
| strand | - |
| ver | v1.2 |
| region | chr2:43812472-43838839 |
| region5000 | chr2:43807472-43843839 |
| regionname0 | ABCG5_chr2_43812472_43838839 |
| regionname5000 | ABCG5_chr2_43807472_43843839 |
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 | 1/1 | 651 | 224 | 46 | 52 | 75 | 15 | 34 | ABCG5_chr2_43807472_43843839 | ABCG5 | MGDLS others(646): Show |
chr2 | 43807472 | 43843839 |
| a0002 | 0/0 | 651 | 70 | 27 | 18 | 13 | 3 | 9 | ABCG5_chr2_43807472_43843839 | ABCG5 | MGDLS others(646): Show |
chr2 | 43807472 | 43843839 |
| a0003 | 0/0 | 651 | 12 | 4 | 3 | 3 | 0 | 2 | ABCG5_chr2_43807472_43843839 | ABCG5 | MGDLS others(646): Show |
chr2 | 43807472 | 43843839 |
| a0004 | 0/0 | 651 | 6 | 2 | 2 | 1 | 0 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | MGDLS others(646): Show |
chr2 | 43807472 | 43843839 |
| a0005 | 0/0 | 651 | 5 | 4 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | MGDLS others(646): Show |
chr2 | 43807472 | 43843839 |
| a0006 | 0/0 | 651 | 5 | 5 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | MGDLS others(646): Show |
chr2 | 43807472 | 43843839 |
| a0007 | 0/0 | 651 | 2 | 2 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | MGDLS others(646): Show |
chr2 | 43807472 | 43843839 |
| a0008 | 0/0 | 651 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | MGDLS others(646): Show |
chr2 | 43807472 | 43843839 |
| a0009 | 0/0 | 651 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | MGDLS others(646): Show |
chr2 | 43807472 | 43843839 |
| a0010 | 0/0 | 651 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | MGDLS others(646): Show |
chr2 | 43807472 | 43843839 |
| a0011 | 0/0 | 651 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | MGDLS others(646): Show |
chr2 | 43807472 | 43843839 |
| a0012 | 0/0 | 651 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | MGDLS others(646): Show |
chr2 | 43807472 | 43843839 |
| a0013 | 0/0 | 651 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | MGDLS others(646): Show |
chr2 | 43807472 | 43843839 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1953 | 221 | 46 | 52 | 73 | 15 | 33 | ABCG5_chr2_43807472_43843839 | ABCG5 | ATGGG others(1948): Show |
chr2 | 43807472 | 43843839 | ||
| a0001c0010 | 0/0 | 1953 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | ATGGG others(1948): Show |
chr2 | 43807472 | 43843839 | ||
| a0001c0013 | 0/0 | 1953 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | ATGGG others(1948): Show |
chr2 | 43807472 | 43843839 | ||
| a0001c0016 | 0/0 | 1953 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | ATGGG others(1948): Show |
chr2 | 43807472 | 43843839 | ||
| a0002c0002 | 0/0 | 1953 | 68 | 26 | 17 | 13 | 3 | 9 | ABCG5_chr2_43807472_43843839 | ABCG5 | ATGGG others(1948): Show |
chr2 | 43807472 | 43843839 | ||
| a0002c0009 | 0/0 | 1953 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | ATGGG others(1948): Show |
chr2 | 43807472 | 43843839 | ||
| a0002c0015 | 0/0 | 1953 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | ATGGG others(1948): Show |
chr2 | 43807472 | 43843839 | ||
| a0003c0003 | 0/0 | 1953 | 12 | 4 | 3 | 3 | 0 | 2 | ABCG5_chr2_43807472_43843839 | ABCG5 | ATGGG others(1948): Show |
chr2 | 43807472 | 43843839 | ||
| a0004c0004 | 0/0 | 1953 | 6 | 2 | 2 | 1 | 0 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | ATGGG others(1948): Show |
chr2 | 43807472 | 43843839 | ||
| a0005c0006 | 0/0 | 1953 | 5 | 4 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | ATGGG others(1948): Show |
chr2 | 43807472 | 43843839 | ||
| a0006c0005 | 0/0 | 1953 | 5 | 5 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | ATGGG others(1948): Show |
chr2 | 43807472 | 43843839 | ||
| a0007c0007 | 0/0 | 1953 | 2 | 2 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | ATGGG others(1948): Show |
chr2 | 43807472 | 43843839 | ||
| a0008c0011 | 0/0 | 1953 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | ATGGG others(1948): Show |
chr2 | 43807472 | 43843839 | ||
| a0009c0017 | 0/0 | 1953 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | ATGGG others(1948): Show |
chr2 | 43807472 | 43843839 | ||
| a0010c0018 | 0/0 | 1953 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | ATGGG others(1948): Show |
chr2 | 43807472 | 43843839 | ||
| a0011c0012 | 0/0 | 1953 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | ATGGG others(1948): Show |
chr2 | 43807472 | 43843839 | ||
| a0012c0014 | 0/0 | 1953 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | ATGGG others(1948): Show |
chr2 | 43807472 | 43843839 | ||
| a0013c0008 | 0/0 | 1953 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | ATGGG others(1948): Show |
chr2 | 43807472 | 43843839 |
| acthapid | grch38/chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2760 | 157 | 16 | 39 | 69 | 9 | 22 | ABCG5_chr2_43807472_43843839 | ABCG5 | AGATA others(2755): Show |
chr2 | 43807472 | 43843839 |
| a0001c0001t0003 | 0/0 | 2760 | 31 | 14 | 7 | 2 | 5 | 3 | ABCG5_chr2_43807472_43843839 | ABCG5 | AGATA others(2755): Show |
chr2 | 43807472 | 43843839 |
| a0001c0001t0004 | 0/0 | 2760 | 10 | 5 | 2 | 2 | 1 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | AGATA others(2755): Show |
chr2 | 43807472 | 43843839 |
| a0001c0001t0005 | 0/0 | 2760 | 9 | 5 | 3 | 0 | 0 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | AGATA others(2755): Show |
chr2 | 43807472 | 43843839 |
| a0001c0001t0006 | 0/0 | 2760 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | AGATA others(2755): Show |
chr2 | 43807472 | 43843839 |
| a0001c0001t0007 | 0/0 | 2760 | 5 | 4 | 0 | 0 | 0 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | AGATA others(2755): Show |
chr2 | 43807472 | 43843839 |
| a0001c0001t0009 | 0/0 | 2760 | 3 | 0 | 0 | 0 | 0 | 3 | ABCG5_chr2_43807472_43843839 | ABCG5 | AGATA others(2755): Show |
chr2 | 43807472 | 43843839 |
| a0001c0001t0010 | 0/0 | 2760 | 2 | 1 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | AGATA others(2755): Show |
chr2 | 43807472 | 43843839 |
| a0001c0001t0011 | 0/0 | 2760 | 2 | 0 | 0 | 0 | 0 | 2 | ABCG5_chr2_43807472_43843839 | ABCG5 | AGATA others(2755): Show |
chr2 | 43807472 | 43843839 |
| a0001c0001t0012 | 0/0 | 2760 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | AGATA others(2755): Show |
chr2 | 43807472 | 43843839 |
| a0001c0010t0004 | 0/0 | 2760 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | AGATA others(2755): Show |
chr2 | 43807472 | 43843839 |
| a0001c0013t0001 | 0/0 | 2760 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | AGATA others(2755): Show |
chr2 | 43807472 | 43843839 |
| a0001c0016t0001 | 0/0 | 2760 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | AGATA others(2755): Show |
chr2 | 43807472 | 43843839 |
| a0002c0002t0002 | 0/0 | 2760 | 66 | 25 | 17 | 12 | 3 | 9 | ABCG5_chr2_43807472_43843839 | ABCG5 | AGATA others(2755): Show |
chr2 | 43807472 | 43843839 |
| a0002c0002t0007 | 0/0 | 2760 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | AGATA others(2755): Show |
chr2 | 43807472 | 43843839 |
| a0002c0002t0008 | 0/0 | 2759 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | AGATA others(2754): Show |
chr2 | 43807472 | 43843839 |
| a0002c0009t0002 | 0/0 | 2760 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | AGATA others(2755): Show |
chr2 | 43807472 | 43843839 |
| a0002c0015t0002 | 0/0 | 2760 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | AGATA others(2755): Show |
chr2 | 43807472 | 43843839 |
| a0003c0003t0001 | 0/0 | 2760 | 9 | 2 | 3 | 3 | 0 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | AGATA others(2755): Show |
chr2 | 43807472 | 43843839 |
| a0003c0003t0003 | 0/0 | 2760 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | AGATA others(2755): Show |
chr2 | 43807472 | 43843839 |
| a0003c0003t0006 | 0/0 | 2760 | 2 | 2 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | AGATA others(2755): Show |
chr2 | 43807472 | 43843839 |
| a0004c0004t0002 | 0/0 | 2760 | 6 | 2 | 2 | 1 | 0 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | AGATA others(2755): Show |
chr2 | 43807472 | 43843839 |
| a0005c0006t0001 | 0/0 | 2760 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | AGATA others(2755): Show |
chr2 | 43807472 | 43843839 |
| a0005c0006t0006 | 0/0 | 2760 | 4 | 3 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | AGATA others(2755): Show |
chr2 | 43807472 | 43843839 |
| a0006c0005t0002 | 0/0 | 2760 | 2 | 2 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | AGATA others(2755): Show |
chr2 | 43807472 | 43843839 |
| a0006c0005t0008 | 0/0 | 2759 | 3 | 3 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | AGATA others(2754): Show |
chr2 | 43807472 | 43843839 |
| a0007c0007t0001 | 0/0 | 2760 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | AGATA others(2755): Show |
chr2 | 43807472 | 43843839 |
| a0007c0007t0003 | 0/0 | 2760 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | AGATA others(2755): Show |
chr2 | 43807472 | 43843839 |
| a0008c0011t0001 | 0/0 | 2760 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | AGATA others(2755): Show |
chr2 | 43807472 | 43843839 |
| a0009c0017t0002 | 0/0 | 2760 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | AGATA others(2755): Show |
chr2 | 43807472 | 43843839 |
| a0010c0018t0004 | 0/0 | 2760 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | AGATA others(2755): Show |
chr2 | 43807472 | 43843839 |
| a0011c0012t0002 | 0/0 | 2760 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | AGATA others(2755): Show |
chr2 | 43807472 | 43843839 |
| a0012c0014t0002 | 0/0 | 2760 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | AGATA others(2755): Show |
chr2 | 43807472 | 43843839 |
| a0013c0008t0002 | 0/0 | 2760 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | AGATA others(2755): Show |
chr2 | 43807472 | 43843839 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 22 | 0 | 5 | 15 | 0 | 2 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0001g0003 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0001g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0001g0006 | 0/0 | 3 | 0 | 0 | 1 | 2 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0001g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0001g0087 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0001g0088 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0003g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0003g0018 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0003g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0003g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0003g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0003g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0003g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0003g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0003g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0003g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0003g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0003g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0003g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0003g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0003g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0003g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0003g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0003g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0003g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0003g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0003g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0003g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0003g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0003g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0003g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0003g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0003g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0004g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0004g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0004g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0004g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0004g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0004g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0004g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0004g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0004g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0005g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0005g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0005g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0005g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0005g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0005g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0005g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0005g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0005g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0006g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0007g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0007g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0007g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0007g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0007g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0009g0039 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0009g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0010g0037 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0011g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0011g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0001t0012g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0010t0004g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0013t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0001c0016t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0002c0002t0002g0002 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0002c0002t0002g0005 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0002c0002t0002g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0002c0002t0002g0015 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0002c0002t0002g0020 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0002c0002t0002g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0002c0002t0002g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0002c0002t0002g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0002c0002t0002g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0002c0002t0002g0036 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0002c0002t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0002c0002t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0002c0002t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0002c0002t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0002c0002t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0002c0002t0002g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0002c0002t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0002c0002t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0002c0002t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0002c0002t0002g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0002c0002t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0002c0002t0002g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0002c0002t0002g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0002c0002t0002g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0002c0002t0002g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0002c0002t0002g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0002c0002t0002g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0002c0002t0002g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0002c0002t0002g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0002c0002t0002g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0002c0002t0002g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0002c0002t0002g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0002c0002t0002g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0002c0002t0002g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0002c0002t0002g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0002c0002t0002g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0002c0002t0002g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0002c0002t0002g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0002c0002t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0002c0002t0002g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0002c0002t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0002c0002t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0002c0002t0002g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0002c0002t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0002c0002t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0002c0002t0002g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0002c0002t0002g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0002c0002t0002g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0002c0002t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0002c0002t0002g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0002c0002t0002g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0002c0002t0002g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0002c0002t0007g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0002c0002t0008g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0002c0009t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0002c0015t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0003c0003t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0003c0003t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0003c0003t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0003c0003t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0003c0003t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0003c0003t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0003c0003t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0003c0003t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0003c0003t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0003c0003t0003g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0003c0003t0006g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0004c0004t0002g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0004c0004t0002g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0004c0004t0002g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0004c0004t0002g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0004c0004t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0004c0004t0002g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0005c0006t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0005c0006t0006g0025 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0005c0006t0006g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0005c0006t0006g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0006c0005t0002g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0006c0005t0008g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0006c0005t0008g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0006c0005t0008g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0007c0007t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0007c0007t0003g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0008c0011t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0009c0017t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0010c0018t0004g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0011c0012t0002g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0012c0014t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| a0013c0008t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| sampleid | haplotypeid | ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0215 | EUR | GBR | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0059 | EUR | GBR | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0017 | EUR | GBR | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0006 | EUR | GBR | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG00280 | hp1 | a0001 | c0001 | t0003 | g0123 | EUR | FIN | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG00280 | hp2 | a0001 | c0001 | t0003 | g0132 | EUR | FIN | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG00323 | hp1 | a0001 | c0001 | t0003 | g0067 | EUR | FIN | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0019 | EUR | FIN | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG00438 | hp1 | a0004 | c0004 | t0002 | g0253 | EAS | CHS | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | CHS | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG00597 | hp1 | a0001 | c0001 | t0003 | g0208 | EAS | CHS | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | CHS | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG00609 | hp1 | a0008 | c0011 | t0001 | g0216 | EAS | CHS | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | CHS | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG00639 | hp2 | a0002 | c0002 | t0002 | g0020 | AMR | PUR | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG00642 | hp2 | a0002 | c0002 | t0002 | g0165 | AMR | PUR | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | CHS | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | CHS | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG00733 | hp1 | a0001 | c0001 | t0003 | g0092 | AMR | PUR | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG00733 | hp2 | a0002 | c0002 | t0002 | g0036 | AMR | PUR | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG00738 | hp1 | a0001 | c0001 | t0004 | g0096 | AMR | PUR | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG00738 | hp2 | a0001 | c0001 | t0003 | g0080 | AMR | PUR | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0053 | AMR | PUR | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG00741 | hp2 | a0003 | c0003 | t0001 | g0245 | AMR | PUR | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG01074 | hp1 | a0001 | c0001 | t0005 | g0233 | AMR | PUR | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG01074 | hp2 | a0002 | c0002 | t0002 | g0055 | AMR | PUR | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG01081 | hp1 | a0002 | c0002 | t0002 | g0030 | AMR | PUR | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG01099 | hp1 | a0002 | c0002 | t0002 | g0164 | AMR | PUR | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG01099 | hp2 | a0001 | c0001 | t0005 | g0232 | AMR | PUR | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG01106 | hp2 | a0001 | c0001 | t0005 | g0182 | AMR | PUR | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG01109 | hp1 | a0001 | c0001 | t0010 | g0037 | AMR | PUR | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG01109 | hp2 | a0001 | c0001 | t0003 | g0066 | AMR | PUR | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG01168 | hp1 | a0002 | c0015 | t0002 | g0063 | AMR | PUR | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG01175 | hp1 | a0001 | c0001 | t0003 | g0018 | AMR | PUR | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | PUR | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG01192 | hp1 | a0002 | c0002 | t0002 | g0138 | AMR | PUR | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG01243 | hp1 | a0005 | c0006 | t0006 | g0025 | AMR | PUR | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG01243 | hp2 | a0002 | c0002 | t0002 | g0082 | AMR | PUR | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | CLM | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | CLM | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | CLM | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG01261 | hp2 | a0001 | c0001 | t0004 | g0065 | AMR | CLM | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | CLM | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | CLM | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0214 | AMR | CLM | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | CLM | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | CLM | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0099 | AMR | CLM | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG01515 | hp1 | a0002 | c0002 | t0002 | g0015 | EUR | IBS | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0014 | EUR | IBS | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0135 | EUR | IBS | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG01516 | hp2 | a0001 | c0001 | t0003 | g0018 | EUR | IBS | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0134 | EUR | IBS | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG01517 | hp2 | a0002 | c0002 | t0002 | g0015 | EUR | IBS | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG01884 | hp1 | a0006 | c0005 | t0008 | g0050 | AFR | ACB | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG01884 | hp2 | a0006 | c0005 | t0002 | g0009 | AFR | ACB | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG01891 | hp1 | a0001 | c0001 | t0005 | g0079 | AFR | ACB | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | ACB | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG01928 | hp1 | a0001 | c0001 | t0003 | g0111 | AMR | PEL | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PEL | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG01934 | hp1 | a0002 | c0002 | t0002 | g0223 | AMR | PEL | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG01943 | hp1 | a0002 | c0002 | t0002 | g0002 | AMR | PEL | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG01943 | hp2 | a0003 | c0003 | t0001 | g0250 | AMR | PEL | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG01952 | hp1 | a0002 | c0002 | t0002 | g0002 | AMR | PEL | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0058 | AMR | PEL | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG01975 | hp1 | a0004 | c0004 | t0002 | g0252 | AMR | PEL | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG01975 | hp2 | a0002 | c0002 | t0002 | g0107 | AMR | PEL | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PEL | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG01978 | hp2 | a0004 | c0004 | t0002 | g0246 | AMR | PEL | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG01981 | hp1 | a0002 | c0002 | t0002 | g0046 | AMR | PEL | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG01981 | hp2 | a0001 | c0001 | t0003 | g0072 | AMR | PEL | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG01993 | hp1 | a0002 | c0002 | t0002 | g0093 | AMR | PEL | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | KHV | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | KHV | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG02040 | hp1 | a0001 | c0001 | t0003 | g0172 | EAS | KHV | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG02055 | hp1 | a0001 | c0001 | t0006 | g0141 | AFR | ACB | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG02055 | hp2 | a0001 | c0001 | t0007 | g0108 | AFR | ACB | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG02074 | hp1 | a0003 | c0003 | t0001 | g0249 | EAS | KHV | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | KHV | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | KHV | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | KHV | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG02132 | hp1 | a0009 | c0017 | t0002 | g0241 | EAS | KHV | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG02132 | hp2 | a0001 | c0001 | t0004 | g0170 | EAS | KHV | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG02145 | hp1 | a0005 | c0006 | t0006 | g0025 | AFR | ACB | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | ACB | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0117 | AMR | PEL | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | CDX | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG02155 | hp2 | a0002 | c0002 | t0002 | g0187 | EAS | CDX | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG02165 | hp1 | a0003 | c0003 | t0001 | g0242 | EAS | CDX | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0236 | AFR | ACB | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG02257 | hp2 | a0001 | c0001 | t0004 | g0105 | AFR | ACB | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG02258 | hp1 | a0001 | c0001 | t0005 | g0084 | AFR | ACB | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG02258 | hp2 | a0005 | c0006 | t0006 | g0158 | AFR | ACB | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG02273 | hp1 | a0002 | c0002 | t0002 | g0002 | AMR | PEL | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG02273 | hp2 | a0003 | c0003 | t0001 | g0244 | AMR | PEL | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0237 | AFR | ACB | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | ACB | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG02293 | hp1 | a0002 | c0002 | t0002 | g0030 | AMR | PEL | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG02293 | hp2 | a0002 | c0002 | t0002 | g0002 | AMR | PEL | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG02300 | hp2 | a0001 | c0001 | t0003 | g0110 | AMR | PEL | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG02451 | hp1 | a0001 | c0001 | t0003 | g0145 | AFR | ACB | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | ACB | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | KHV | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG02572 | hp1 | a0001 | c0001 | t0004 | g0021 | AFR | GWD | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0183 | AFR | GWD | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0070 | SAS | PJL | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0129 | SAS | PJL | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG02622 | hp1 | a0002 | c0002 | t0002 | g0026 | AFR | GWD | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG02622 | hp2 | a0001 | c0001 | t0005 | g0076 | AFR | GWD | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG02630 | hp1 | a0001 | c0001 | t0003 | g0147 | AFR | GWD | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG02630 | hp2 | a0002 | c0002 | t0002 | g0078 | AFR | GWD | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG02647 | hp1 | a0001 | c0001 | t0005 | g0234 | AFR | GWD | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG02647 | hp2 | a0002 | c0002 | t0002 | g0005 | AFR | GWD | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0184 | SAS | PJL | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0115 | SAS | PJL | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG02698 | hp1 | a0002 | c0002 | t0002 | g0125 | SAS | PJL | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG02698 | hp2 | a0001 | c0001 | t0003 | g0095 | SAS | PJL | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG02717 | hp1 | a0001 | c0001 | t0003 | g0126 | AFR | GWD | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG02717 | hp2 | a0002 | c0009 | t0002 | g0042 | AFR | GWD | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG02723 | hp1 | a0001 | c0001 | t0003 | g0027 | AFR | GWD | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG02723 | hp2 | a0001 | c0001 | t0003 | g0226 | AFR | GWD | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0089 | SAS | PJL | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0206 | SAS | PJL | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0116 | SAS | PJL | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG02738 | hp2 | a0002 | c0002 | t0002 | g0222 | SAS | PJL | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG02809 | hp1 | a0006 | c0005 | t0002 | g0009 | AFR | GWD | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0230 | AFR | GWD | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG02818 | hp1 | a0007 | c0007 | t0003 | g0257 | AFR | GWD | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG02818 | hp2 | a0003 | c0003 | t0001 | g0239 | AFR | GWD | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG02886 | hp1 | a0001 | c0001 | t0003 | g0027 | AFR | GWD | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG02886 | hp2 | a0002 | c0002 | t0002 | g0128 | AFR | GWD | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG02895 | hp2 | a0005 | c0006 | t0006 | g0157 | AFR | GWD | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG02896 | hp1 | a0001 | c0001 | t0003 | g0148 | AFR | GWD | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG02896 | hp2 | a0002 | c0002 | t0002 | g0010 | AFR | GWD | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG02897 | hp2 | a0002 | c0002 | t0002 | g0010 | AFR | GWD | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG02922 | hp1 | a0010 | c0018 | t0004 | g0258 | AFR | ESN | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG02922 | hp2 | a0011 | c0012 | t0002 | g0113 | AFR | ESN | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG02976 | hp1 | a0002 | c0002 | t0002 | g0166 | AFR | ESN | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG02976 | hp2 | a0006 | c0005 | t0008 | g0049 | AFR | ESN | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG03017 | hp2 | a0002 | c0002 | t0002 | g0205 | SAS | PJL | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | GWD | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG03041 | hp2 | a0001 | c0001 | t0007 | g0227 | AFR | GWD | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG03098 | hp1 | a0003 | c0003 | t0001 | g0248 | AFR | MSL | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG03098 | hp2 | a0002 | c0002 | t0002 | g0146 | AFR | MSL | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG03130 | hp1 | a0002 | c0002 | t0002 | g0005 | AFR | ESN | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG03130 | hp2 | a0002 | c0002 | t0002 | g0190 | AFR | ESN | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0231 | AFR | ESN | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG03139 | hp2 | a0012 | c0014 | t0002 | g0162 | AFR | ESN | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG03195 | hp1 | a0002 | c0002 | t0002 | g0181 | AFR | ESN | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG03195 | hp2 | a0013 | c0008 | t0002 | g0041 | AFR | ESN | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG03209 | hp1 | a0003 | c0003 | t0006 | g0038 | AFR | MSL | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG03209 | hp2 | a0002 | c0002 | t0002 | g0154 | AFR | MSL | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG03225 | hp1 | a0002 | c0002 | t0002 | g0083 | AFR | MSL | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG03225 | hp2 | a0005 | c0006 | t0001 | g0160 | AFR | MSL | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0068 | SAS | PJL | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG03239 | hp2 | a0002 | c0002 | t0002 | g0136 | SAS | PJL | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG03453 | hp1 | a0006 | c0005 | t0008 | g0043 | AFR | MSL | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG03453 | hp2 | a0001 | c0001 | t0005 | g0077 | AFR | MSL | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG03486 | hp1 | a0002 | c0002 | t0002 | g0143 | AFR | MSL | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG03486 | hp2 | a0001 | c0001 | t0004 | g0161 | AFR | MSL | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG03490 | hp2 | a0001 | c0001 | t0011 | g0260 | SAS | PJL | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG03491 | hp2 | a0004 | c0004 | t0002 | g0254 | SAS | PJL | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG03516 | hp1 | a0002 | c0002 | t0002 | g0048 | AFR | ESN | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | ESN | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0235 | AFR | GWD | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG03540 | hp2 | a0002 | c0002 | t0002 | g0103 | AFR | GWD | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | MSL | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG03579 | hp2 | a0001 | c0001 | t0010 | g0037 | AFR | MSL | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0086 | SAS | PJL | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG03654 | hp2 | a0002 | c0002 | t0002 | g0036 | SAS | PJL | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG03688 | hp1 | a0001 | c0001 | t0003 | g0173 | SAS | STU | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG03688 | hp2 | a0002 | c0002 | t0002 | g0137 | SAS | STU | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG03704 | hp1 | a0001 | c0001 | t0011 | g0259 | SAS | PJL | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0085 | SAS | PJL | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG03710 | hp1 | a0001 | c0001 | t0009 | g0039 | SAS | PJL | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG03710 | hp2 | a0001 | c0001 | t0003 | g0229 | SAS | PJL | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0194 | SAS | BEB | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG03831 | hp2 | a0001 | c0001 | t0009 | g0261 | SAS | BEB | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG03834 | hp1 | a0003 | c0003 | t0003 | g0251 | SAS | BEB | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0179 | SAS | BEB | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0200 | SAS | BEB | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0221 | SAS | BEB | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG03942 | hp2 | a0001 | c0001 | t0007 | g0225 | SAS | BEB | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG04115 | hp1 | a0001 | c0001 | t0009 | g0039 | SAS | STU | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG04115 | hp2 | a0002 | c0002 | t0002 | g0124 | SAS | STU | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG04184 | hp1 | a0002 | c0002 | t0002 | g0201 | SAS | BEB | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG04184 | hp2 | a0003 | c0003 | t0001 | g0240 | SAS | BEB | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG04204 | hp1 | a0001 | c0001 | t0005 | g0202 | SAS | STU | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0075 | SAS | STU | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG04228 | hp1 | a0001 | c0016 | t0001 | g0217 | SAS | STU | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG04228 | hp2 | a0002 | c0002 | t0002 | g0197 | SAS | STU | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| NA18522 | hp1 | a0001 | c0001 | t0007 | g0150 | AFR | YRI | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| NA18522 | hp2 | a0001 | c0001 | t0004 | g0021 | AFR | YRI | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| NA18906 | hp1 | a0001 | c0001 | t0004 | g0149 | AFR | YRI | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| NA18906 | hp2 | a0001 | c0001 | t0003 | g0081 | AFR | YRI | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| NA18952 | hp1 | a0002 | c0002 | t0002 | g0035 | EAS | JPT | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| NA18962 | hp1 | a0002 | c0002 | t0002 | g0034 | EAS | JPT | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| NA18964 | hp1 | a0002 | c0002 | t0002 | g0061 | EAS | JPT | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| NA18968 | hp1 | a0003 | c0003 | t0001 | g0247 | EAS | JPT | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| NA18977 | hp2 | a0002 | c0002 | t0002 | g0185 | EAS | JPT | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| NA18979 | hp1 | a0002 | c0002 | t0002 | g0195 | EAS | JPT | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| NA18982 | hp1 | a0002 | c0002 | t0002 | g0034 | EAS | JPT | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| NA18982 | hp2 | a0001 | c0013 | t0001 | g0198 | EAS | JPT | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| NA19002 | hp1 | a0002 | c0002 | t0002 | g0035 | EAS | JPT | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| NA19005 | hp1 | a0002 | c0002 | t0007 | g0121 | EAS | JPT | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| NA19009 | hp1 | a0002 | c0002 | t0002 | g0209 | EAS | JPT | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| NA19012 | hp1 | a0002 | c0002 | t0002 | g0060 | EAS | JPT | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| NA19012 | hp2 | a0001 | c0010 | t0004 | g0186 | EAS | JPT | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| NA19030 | hp1 | a0002 | c0002 | t0002 | g0005 | AFR | LWK | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| NA19030 | hp2 | a0004 | c0004 | t0002 | g0238 | AFR | LWK | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| NA19043 | hp1 | a0002 | c0002 | t0002 | g0100 | AFR | LWK | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| NA19043 | hp2 | a0007 | c0007 | t0001 | g0256 | AFR | LWK | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| NA19056 | hp1 | a0001 | c0001 | t0004 | g0204 | EAS | JPT | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| NA19068 | hp2 | a0002 | c0002 | t0002 | g0175 | EAS | JPT | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| NA19085 | hp1 | a0002 | c0002 | t0002 | g0090 | EAS | JPT | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | YRI | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| NA19240 | hp2 | a0002 | c0002 | t0002 | g0189 | AFR | YRI | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| NA20129 | hp1 | a0004 | c0004 | t0002 | g0243 | AFR | ASW | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| NA20129 | hp2 | a0002 | c0002 | t0002 | g0127 | AFR | ASW | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| NA20752 | hp1 | a0002 | c0002 | t0002 | g0020 | EUR | TSI | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| NA20752 | hp2 | a0001 | c0001 | t0003 | g0064 | EUR | TSI | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| NA20805 | hp1 | a0001 | c0001 | t0004 | g0255 | EUR | TSI | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0006 | EUR | TSI | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0122 | SAS | GIH | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| NA20905 | hp2 | a0001 | c0001 | t0012 | g0040 | SAS | GIH | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | CLM | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | CLM | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG02109 | hp1 | a0002 | c0002 | t0002 | g0224 | AFR | ACB | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG02109 | hp2 | a0001 | c0001 | t0007 | g0156 | AFR | ACB | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0212 | AFR | ACB | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG02486 | hp2 | a0001 | c0001 | t0003 | g0151 | AFR | ACB | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG02559 | hp1 | a0002 | c0002 | t0002 | g0153 | AFR | ACB | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG02559 | hp2 | a0002 | c0002 | t0002 | g0104 | AFR | ACB | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG03471 | hp1 | a0002 | c0002 | t0002 | g0026 | AFR | MSL | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG03471 | hp2 | a0003 | c0003 | t0006 | g0038 | AFR | MSL | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG06807 | hp1 | a0002 | c0002 | t0002 | g0005 | AFR | USA | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| HG06807 | hp2 | a0001 | c0001 | t0003 | g0011 | AFR | USA | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| NA20300 | hp1 | a0001 | c0001 | t0003 | g0155 | AFR | USA | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| NA20300 | hp2 | a0001 | c0001 | t0003 | g0011 | AFR | USA | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| NA21309 | hp1 | a0001 | c0001 | t0003 | g0102 | AFR | LWK | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| NA21309 | hp2 | a0002 | c0002 | t0008 | g0144 | AFR | LWK | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0087 | REF | REF | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0088 | REF | REF | ABCG5_chr2_43807472_43843839 | ABCG5 | chr2 | 43807472 | 43843839 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:43813262 | G | C | 7 | a0002a0004a0006others(4): Show | 85 | HG00438.hp1 HG00639.hp2 HG00642.hp2 others(82): Show |
missense_variant | MODERATE | c.1810C>G | p.Gln604Glu | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 13/13 | 1970/2760 | 1810/1956 | 604/651 | chr2 | 43813262 | |||
| chr2:43819994 | C | T | 1 | a0008 | 1 | HG00609.hp1 | missense_variant | MODERATE | c.1570G>A | p.Val524Ile | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/13 | 1730/2760 | 1570/1956 | 524/651 | chr2 | 43819994 | |||
| chr2:43820014 | G | C | 2 | a0010a0011 | 2 | HG02922.hp1 HG02922.hp2 |
missense_variant | MODERATE | c.1550C>G | p.Thr517Ser | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/13 | 1710/2760 | 1550/1956 | 517/651 | chr2 | 43820014 | |||
| chr2:43820036 | G | T | 1 | a0009 | 1 | HG02132.hp1 | missense_variant | MODERATE | c.1528C>A | p.His510Asn | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/13 | 1688/2760 | 1528/1956 | 510/651 | chr2 | 43820036 | |||
| chr2:43824009 | T | G | 1 | a0006 | 5 | HG01884.hp1 HG01884.hp2 HG02809.hp1 others(2): Show |
missense_variant | MODERATE | c.1228A>C | p.Asn410His | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 9/13 | 1388/2760 | 1228/1956 | 410/651 | chr2 | 43824009 | |||
| chr2:43825008 | T | C | 2 | a0005a0012 | 6 | HG01243.hp1 HG02145.hp1 HG02258.hp2 others(3): Show |
missense_variant | MODERATE | c.785A>G | p.Lys262Arg | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 7/13 | 945/2760 | 785/1956 | 262/651 | chr2 | 43825008 | |||
| chr2:43837951 | G | A | 3 | a0003a0004a0009 | 19 | HG00438.hp1 HG00741.hp2 HG01943.hp2 others(16): Show |
missense_variant | MODERATE | c.148C>T | p.Arg50Cys | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/13 | 308/2760 | 148/1956 | 50/651 | chr2 | 43837951 | |||
| chr2:43838541 | C | A | 2 | a0007a0010 | 3 | HG02818.hp1 HG02922.hp1 NA19043.hp2 |
missense_variant | MODERATE | c.139G>T | p.Val47Phe | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 1/13 | 299/2760 | 139/1956 | 47/651 | chr2 | 43838541 | |||
| chr2:43838630 | A | C | 1 | a0013 | 1 | HG03195.hp2 | missense_variant | MODERATE | c.50T>G | p.Val17Gly | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 1/13 | 210/2760 | 50/1956 | 17/651 | chr2 | 43838630 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:43822835 | G | A | 1 | a0001c0013 | 1 | NA18982.hp2 | synonymous_variant | LOW | c.1425C>T | p.Ser475Ser | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 10/13 | 1585/2760 | 1425/1956 | 475/651 | chr2 | 43822835 | |||
| chr2:43826460 | G | A | 1 | a0002c0015 | 1 | HG01168.hp1 | synonymous_variant | LOW | c.696C>T | p.Val232Val | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 6/13 | 856/2760 | 696/1956 | 232/651 | chr2 | 43826460 | |||
| chr2:43828011 | G | A | 1 | a0001c0016 | 1 | HG04228.hp1 | synonymous_variant | LOW | c.606C>T | p.Ser202Ser | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 5/13 | 766/2760 | 606/1956 | 202/651 | chr2 | 43828011 | |||
| chr2:43832010 | C | T | 1 | a0001c0010 | 1 | NA19012.hp2 | synonymous_variant | LOW | c.339G>A | p.Val113Val | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 3/13 | 499/2760 | 339/1956 | 113/651 | chr2 | 43832010 | |||
| chr2:43838581 | C | T | 1 | a0002c0009 | 1 | HG02717.hp2 | synonymous_variant | LOW | c.99G>A | p.Pro33Pro | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 1/13 | 259/2760 | 99/1956 | 33/651 | chr2 | 43838581 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:43812494 | G | A | 15 | a0001c0001t0004a0001c0001t0010a0001c0010t0004others(12): Show | 98 | HG00438.hp1 HG00639.hp2 HG00642.hp2 others(95): Show |
3_prime_UTR_variant | MODIFIER | c.*622C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 13/13 | 622 | chr2 | 43812494 | ||||||
| chr2:43812581 | G | A | 3 | a0001c0001t0006a0003c0003t0006a0005c0006t0006 | 7 | HG01243.hp1 HG02055.hp1 HG02145.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*535C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 13/13 | 535 | chr2 | 43812581 | ||||||
| chr2:43812594 | C | T | 5 | a0001c0001t0003a0001c0001t0005a0001c0001t0009others(2): Show | 45 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*522G>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 13/13 | 522 | chr2 | 43812594 | ||||||
| chr2:43812700 | C | T | 12 | a0001c0001t0010a0002c0002t0002a0002c0002t0008others(9): Show | 86 | HG00438.hp1 HG00639.hp2 HG00642.hp2 others(83): Show |
3_prime_UTR_variant | MODIFIER | c.*416G>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 13/13 | 416 | chr2 | 43812700 | ||||||
| chr2:43812717 | G | A | 1 | a0001c0001t0005 | 9 | HG01074.hp1 HG01099.hp2 HG01106.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*399C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 13/13 | 399 | chr2 | 43812717 | ||||||
| chr2:43812736 | A | C | 23 | a0001c0001t0003a0001c0001t0004a0001c0001t0005others(20): Show | 151 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(148): Show |
3_prime_UTR_variant | MODIFIER | c.*380T>G | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 13/13 | 380 | chr2 | 43812736 | ||||||
| chr2:43812896 | TA | T | 2 | a0002c0002t0008a0006c0005t0008 | 4 | HG01884.hp1 HG02976.hp2 HG03453.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*219delT | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 13/13 | 219 | chr2 | 43812896 | ||||||
| chr2:43813044 | C | T | 1 | a0001c0001t0010 | 2 | HG01109.hp1 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*72G>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 13/13 | 72 | chr2 | 43813044 | ||||||
| chr2:43838781 | C | T | 1 | a0001c0001t0012 | 1 | NA20905.hp2 | 5_prime_UTR_variant | MODIFIER | c.-102G>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 1/13 | 102 | chr2 | 43838781 | ||||||
| chr2:43838797 | T | G | 2 | a0001c0001t0009a0001c0001t0011 | 5 | HG03490.hp2 HG03704.hp1 HG03710.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-118A>C | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 1/13 | 118 | chr2 | 43838797 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:43813358 | T | C | 1 | a0001c0001t0003g0148 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1763-49A>G | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 12/12 | chr2 | 43813358 | |||||||
| chr2:43813423 | G | C | 11 | a0001c0001t0004g0021a0001c0001t0004g0065a0001c0001t0004g0096others(8): Show | 12 | HG00738.hp1 HG01261.hp2 HG02132.hp2 others(9): Show |
intron_variant | MODIFIER | c.1763-114C>G | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 12/12 | chr2 | 43813423 | |||||||
| chr2:43813426 | A | G | 1 | a0002c0002t0002g0104 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1763-117T>C | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 12/12 | chr2 | 43813426 | |||||||
| chr2:43813519 | A | G | 11 | a0001c0001t0004g0021a0001c0001t0004g0065a0001c0001t0004g0096others(8): Show | 12 | HG00738.hp1 HG01261.hp2 HG02132.hp2 others(9): Show |
intron_variant | MODIFIER | c.1763-210T>C | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 12/12 | chr2 | 43813519 | |||||||
| chr2:43813542 | A | C | 2 | a0001c0001t0003g0027a0001c0001t0003g0226 | 3 | HG02723.hp1 HG02723.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1763-233T>G | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 12/12 | chr2 | 43813542 | |||||||
| chr2:43813674 | G | GT | 13 | a0001c0001t0003g0208a0001c0001t0004g0021a0001c0001t0004g0065others(10): Show | 14 | HG00597.hp1 HG00738.hp1 HG00741.hp2 others(11): Show |
intron_variant | MODIFIER | c.1763-366dupA | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 12/12 | chr2 | 43813674 | |||||||
| chr2:43813693 | T | G | 15 | a0001c0001t0001g0047a0001c0001t0003g0011a0001c0001t0003g0080others(12): Show | 17 | HG00738.hp1 HG00738.hp2 HG01261.hp2 others(14): Show |
intron_variant | MODIFIER | c.1763-384A>C | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 12/12 | chr2 | 43813693 | |||||||
| chr2:43813697 | G | GT | 7 | a0001c0001t0001g0062a0001c0001t0001g0207a0001c0001t0001g0230others(4): Show | 7 | HG02083.hp1 HG02083.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.1763-389dupA | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 12/12 | chr2 | 43813697 | |||||||
| chr2:43813697 | G | T | 66 | a0002c0002t0002g0002a0002c0002t0002g0005a0002c0002t0002g0010others(63): Show | 81 | HG00438.hp1 HG00639.hp2 HG00642.hp2 others(78): Show |
intron_variant | MODIFIER | c.1763-388C>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 12/12 | chr2 | 43813697 | |||||||
| chr2:43813708 | C | G | 1 | a0001c0001t0007g0108 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1763-399G>C | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 12/12 | chr2 | 43813708 | |||||||
| chr2:43813708 | C | T | 6 | a0001c0001t0007g0150a0001c0001t0007g0156a0001c0001t0007g0225others(3): Show | 6 | HG02109.hp2 HG03041.hp2 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.1763-399G>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 12/12 | chr2 | 43813708 | |||||||
| chr2:43813708 | CGTTTT | C | 11 | a0001c0001t0004g0021a0001c0001t0004g0065a0001c0001t0004g0096others(8): Show | 12 | HG00738.hp1 HG01261.hp2 HG02132.hp2 others(9): Show |
intron_variant | MODIFIER | c.1763-404_1763-400d others(7): Show |
ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 12/12 | chr2 | 43813708 | |||||||
| chr2:43813709 | G | GT | 56 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(53): Show | 61 | HG00438.hp2 HG00639.hp2 HG00642.hp1 others(58): Show |
intron_variant | MODIFIER | c.1763-401dupA | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 12/12 | chr2 | 43813709 | |||||||
| chr2:43813709 | G | GTT | 35 | a0001c0001t0001g0159a0002c0002t0002g0002a0002c0002t0002g0010others(32): Show | 41 | HG00438.hp1 HG00642.hp2 HG00733.hp2 others(38): Show |
intron_variant | MODIFIER | c.1763-402_1763-401d others(4): Show |
ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 12/12 | chr2 | 43813709 | |||||||
| chr2:43813709 | G | GTTT | 18 | a0002c0002t0002g0002a0002c0002t0002g0026a0002c0002t0002g0030others(15): Show | 19 | HG01081.hp1 HG01243.hp2 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.1763-403_1763-401d others(5): Show |
ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 12/12 | chr2 | 43813709 | |||||||
| chr2:43813709 | G | T | 4 | a0001c0001t0007g0108a0001c0001t0007g0227a0001c0001t0011g0260others(1): Show | 4 | HG01168.hp1 HG02055.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1763-400C>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 12/12 | chr2 | 43813709 | |||||||
| chr2:43813709 | GT | G | 33 | a0001c0001t0001g0001a0001c0001t0001g0032a0001c0001t0003g0011others(30): Show | 35 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(32): Show |
intron_variant | MODIFIER | c.1763-401delA | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 12/12 | chr2 | 43813709 | |||||||
| chr2:43813709 | GTTTTTTT others(3): Show |
G | 1 | a0002c0002t0002g0005 | 4 | HG02647.hp2 HG03130.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1763-410_1763-401d others(12): Show |
ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 12/12 | chr2 | 43813709 | |||||||
| chr2:43813710 | T | G | 2 | a0001c0001t0007g0227a0001c0001t0011g0260 | 2 | HG03041.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.1763-401A>C | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 12/12 | chr2 | 43813710 | |||||||
| chr2:43813714 | T | A | 11 | a0001c0001t0004g0021a0001c0001t0004g0065a0001c0001t0004g0096others(8): Show | 12 | HG00738.hp1 HG01261.hp2 HG02132.hp2 others(9): Show |
intron_variant | MODIFIER | c.1763-405A>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 12/12 | chr2 | 43813714 | |||||||
| chr2:43813771 | G | T | 1 | a0002c0002t0002g0005 | 4 | HG02647.hp2 HG03130.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1763-462C>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 12/12 | chr2 | 43813771 | |||||||
| chr2:43813881 | G | A | 1 | a0002c0002t0002g0137 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1763-572C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 12/12 | chr2 | 43813881 | |||||||
| chr2:43813970 | A | C | 11 | a0001c0001t0004g0021a0001c0001t0004g0065a0001c0001t0004g0096others(8): Show | 12 | HG00738.hp1 HG01261.hp2 HG02132.hp2 others(9): Show |
intron_variant | MODIFIER | c.1762+507T>G | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 12/12 | chr2 | 43813970 | |||||||
| chr2:43813971 | C | T | 7 | a0001c0001t0007g0108a0001c0001t0007g0150a0001c0001t0007g0156others(4): Show | 7 | HG02055.hp2 HG02109.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.1762+506G>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 12/12 | chr2 | 43813971 | |||||||
| chr2:43814007 | T | C | 11 | a0001c0001t0004g0021a0001c0001t0004g0065a0001c0001t0004g0096others(8): Show | 12 | HG00738.hp1 HG01261.hp2 HG02132.hp2 others(9): Show |
intron_variant | MODIFIER | c.1762+470A>G | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 12/12 | chr2 | 43814007 | |||||||
| chr2:43814051 | T | C | 11 | a0001c0001t0004g0021a0001c0001t0004g0065a0001c0001t0004g0096others(8): Show | 12 | HG00738.hp1 HG01261.hp2 HG02132.hp2 others(9): Show |
intron_variant | MODIFIER | c.1762+426A>G | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 12/12 | chr2 | 43814051 | |||||||
| chr2:43814065 | A | G | 11 | a0001c0001t0004g0021a0001c0001t0004g0065a0001c0001t0004g0096others(8): Show | 12 | HG00738.hp1 HG01261.hp2 HG02132.hp2 others(9): Show |
intron_variant | MODIFIER | c.1762+412T>C | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 12/12 | chr2 | 43814065 | |||||||
| chr2:43814069 | G | A | 5 | a0001c0001t0003g0066a0001c0001t0003g0067a0001c0001t0003g0072others(2): Show | 5 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(2): Show |
intron_variant | MODIFIER | c.1762+408C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 12/12 | chr2 | 43814069 | |||||||
| chr2:43814086 | G | T | 11 | a0001c0001t0004g0021a0001c0001t0004g0065a0001c0001t0004g0096others(8): Show | 12 | HG00738.hp1 HG01261.hp2 HG02132.hp2 others(9): Show |
intron_variant | MODIFIER | c.1762+391C>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 12/12 | chr2 | 43814086 | |||||||
| chr2:43814118 | G | A | 4 | a0002c0002t0008g0144a0006c0005t0008g0043a0006c0005t0008g0049others(1): Show | 4 | HG01884.hp1 HG02976.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1762+359C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 12/12 | chr2 | 43814118 | |||||||
| chr2:43814122 | G | A | 1 | a0001c0001t0003g0148 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1762+355C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 12/12 | chr2 | 43814122 | |||||||
| chr2:43814140 | C | T | 11 | a0001c0001t0004g0021a0001c0001t0004g0065a0001c0001t0004g0096others(8): Show | 12 | HG00738.hp1 HG01261.hp2 HG02132.hp2 others(9): Show |
intron_variant | MODIFIER | c.1762+337G>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 12/12 | chr2 | 43814140 | |||||||
| chr2:43814160 | C | T | 2 | a0002c0002t0002g0143a0002c0002t0002g0146 | 2 | HG03098.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1762+317G>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 12/12 | chr2 | 43814160 | |||||||
| chr2:43814269 | C | A | 1 | a0001c0001t0001g0191 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1762+208G>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 12/12 | chr2 | 43814269 | |||||||
| chr2:43814345 | A | T | 2 | a0001c0001t0001g0199a0001c0001t0001g0211 | 2 | HG02523.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.1762+132T>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 12/12 | chr2 | 43814345 | |||||||
| chr2:43814669 | T | C | 1 | a0009c0017t0002g0241 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1650-80A>G | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43814669 | |||||||
| chr2:43814755 | T | G | 12 | a0001c0001t0004g0021a0001c0001t0004g0065a0001c0001t0004g0096others(9): Show | 13 | HG00738.hp1 HG01261.hp2 HG02132.hp2 others(10): Show |
intron_variant | MODIFIER | c.1650-166A>C | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43814755 | |||||||
| chr2:43814925 | A | G | 1 | a0001c0001t0001g0206 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1650-336T>C | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43814925 | |||||||
| chr2:43815027 | T | C | 1 | a0001c0001t0004g0096 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1650-438A>G | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43815027 | |||||||
| chr2:43815047 | G | A | 3 | a0001c0001t0001g0044a0001c0001t0001g0112a0001c0001t0001g0119 | 3 | NA18942.hp2 NA18959.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.1650-458C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43815047 | |||||||
| chr2:43815076 | C | A | 5 | a0002c0002t0002g0138a0002c0002t0002g0181a0002c0002t0002g0189others(2): Show | 5 | HG01192.hp1 HG03130.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1650-487G>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43815076 | |||||||
| chr2:43815124 | C | T | 129 | a0001c0001t0003g0011a0001c0001t0003g0018a0001c0001t0003g0027others(126): Show | 150 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.1650-535G>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43815124 | |||||||
| chr2:43815139 | C | G | 1 | a0001c0001t0010g0037 | 2 | HG01109.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1650-550G>C | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43815139 | |||||||
| chr2:43815178 | A | G | 58 | a0001c0001t0001g0071a0001c0001t0001g0094a0001c0001t0004g0021others(55): Show | 72 | HG00438.hp1 HG00642.hp2 HG00733.hp2 others(69): Show |
intron_variant | MODIFIER | c.1650-589T>C | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43815178 | |||||||
| chr2:43815222 | A | G | 1 | a0001c0001t0001g0118 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1650-633T>C | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43815222 | |||||||
| chr2:43815292 | G | A | 129 | a0001c0001t0003g0011a0001c0001t0003g0018a0001c0001t0003g0027others(126): Show | 150 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.1650-703C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43815292 | |||||||
| chr2:43815303 | T | C | 1 | a0002c0002t0002g0166 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1650-714A>G | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43815303 | |||||||
| chr2:43815421 | T | C | 11 | a0001c0001t0004g0021a0001c0001t0004g0065a0001c0001t0004g0096others(8): Show | 12 | HG00738.hp1 HG01261.hp2 HG02132.hp2 others(9): Show |
intron_variant | MODIFIER | c.1650-832A>G | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43815421 | |||||||
| chr2:43815454 | A | T | 1 | a0001c0001t0001g0047 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1650-865T>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43815454 | |||||||
| chr2:43815575 | G | A | 1 | a0001c0001t0001g0178 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1650-986C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43815575 | |||||||
| chr2:43815700 | G | C | 4 | a0001c0001t0004g0021a0001c0001t0004g0096a0001c0001t0004g0149others(1): Show | 5 | HG00738.hp1 HG02572.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1650-1111C>G | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43815700 | |||||||
| chr2:43815707 | A | G | 6 | a0001c0001t0001g0003a0001c0001t0001g0022a0001c0001t0001g0045others(3): Show | 10 | HG00735.hp1 HG01081.hp2 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.1650-1118T>C | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43815707 | |||||||
| chr2:43815757 | A | G | 21 | a0002c0002t0002g0015a0002c0002t0002g0020a0002c0002t0002g0046others(18): Show | 23 | HG00639.hp2 HG01074.hp2 HG01192.hp1 others(20): Show |
intron_variant | MODIFIER | c.1650-1168T>C | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43815757 | |||||||
| chr2:43815765 | C | A | 55 | a0001c0001t0004g0021a0001c0001t0004g0065a0001c0001t0004g0096others(52): Show | 69 | HG00438.hp1 HG00642.hp2 HG00733.hp2 others(66): Show |
intron_variant | MODIFIER | c.1650-1176G>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43815765 | |||||||
| chr2:43815790 | TG | T | 2 | a0001c0001t0003g0027a0001c0001t0003g0226 | 3 | HG02723.hp1 HG02723.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1650-1202delC | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43815790 | |||||||
| chr2:43815861 | C | T | 1 | a0002c0002t0002g0136 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1650-1272G>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43815861 | |||||||
| chr2:43815910 | G | GA | 13 | a0001c0001t0001g0052a0001c0001t0001g0236a0001c0001t0007g0108others(10): Show | 13 | HG01175.hp2 HG01884.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.1650-1322dupT | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43815910 | |||||||
| chr2:43815910 | G | GAA | 96 | a0001c0001t0003g0011a0001c0001t0003g0018a0001c0001t0003g0027others(93): Show | 114 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(111): Show |
intron_variant | MODIFIER | c.1650-1323_1650-132 others(6): Show |
ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43815910 | |||||||
| chr2:43815910 | G | GAAA | 15 | a0001c0001t0003g0126a0001c0001t0004g0021a0001c0001t0004g0065others(12): Show | 16 | HG00738.hp1 HG01261.hp2 HG01978.hp2 others(13): Show |
intron_variant | MODIFIER | c.1650-1324_1650-132 others(7): Show |
ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43815910 | |||||||
| chr2:43815925 | AAAG | A | 5 | a0002c0002t0002g0010a0002c0002t0002g0103a0002c0002t0002g0104others(2): Show | 6 | HG00642.hp2 HG01099.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.1650-1339_1650-133 others(7): Show |
ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43815925 | |||||||
| chr2:43815928 | G | A | 1 | a0001c0001t0010g0037 | 2 | HG01109.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1650-1339C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43815928 | |||||||
| chr2:43815947 | G | T | 1 | a0003c0003t0001g0239 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1650-1358C>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43815947 | |||||||
| chr2:43815975 | A | C | 12 | a0001c0001t0001g0008a0001c0001t0001g0028a0001c0001t0001g0029others(9): Show | 15 | HG02257.hp1 HG02280.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.1650-1386T>G | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43815975 | |||||||
| chr2:43815996 | T | G | 53 | a0001c0001t0001g0116a0001c0001t0003g0155a0001c0001t0004g0021others(50): Show | 66 | HG00438.hp1 HG00733.hp2 HG00738.hp1 others(63): Show |
intron_variant | MODIFIER | c.1650-1407A>C | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43815996 | |||||||
| chr2:43816094 | A | T | 1 | a0001c0001t0010g0037 | 2 | HG01109.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1650-1505T>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43816094 | |||||||
| chr2:43816139 | T | C | 1 | a0001c0001t0001g0183 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1650-1550A>G | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43816139 | |||||||
| chr2:43816220 | T | C | 1 | a0001c0001t0001g0140 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1650-1631A>G | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43816220 | |||||||
| chr2:43816254 | G | A | 45 | a0001c0001t0001g0016a0001c0001t0001g0068a0001c0001t0001g0192others(42): Show | 58 | HG00438.hp1 HG00733.hp2 HG01081.hp1 others(55): Show |
intron_variant | MODIFIER | c.1650-1665C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43816254 | |||||||
| chr2:43816313 | A | T | 113 | a0001c0001t0001g0192a0001c0001t0003g0011a0001c0001t0003g0018others(110): Show | 133 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.1650-1724T>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43816313 | |||||||
| chr2:43816433 | G | A | 2 | a0001c0001t0003g0027a0001c0001t0003g0226 | 3 | HG02723.hp1 HG02723.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1650-1844C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43816433 | |||||||
| chr2:43816433 | GGA | G | 33 | a0001c0001t0001g0045a0001c0001t0001g0109a0002c0002t0002g0002others(30): Show | 39 | HG00438.hp1 HG00639.hp2 HG01074.hp2 others(36): Show |
intron_variant | MODIFIER | c.1650-1846_1650-184 others(6): Show |
ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43816433 | |||||||
| chr2:43816482 | C | T | 3 | a0002c0002t0008g0144a0006c0005t0008g0049a0006c0005t0008g0050 | 3 | HG01884.hp1 HG02976.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1650-1893G>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43816482 | |||||||
| chr2:43816701 | A | C | 6 | a0002c0002t0002g0005a0002c0002t0002g0010a0002c0002t0002g0103others(3): Show | 10 | HG00642.hp2 HG01099.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.1650-2112T>G | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43816701 | |||||||
| chr2:43816755 | T | C | 4 | a0001c0001t0001g0014a0001c0001t0001g0091a0001c0001t0001g0130others(1): Show | 5 | HG01192.hp2 HG01255.hp2 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.1650-2166A>G | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43816755 | |||||||
| chr2:43816816 | T | G | 1 | a0001c0001t0003g0111 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1650-2227A>C | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43816816 | |||||||
| chr2:43817097 | C | T | 9 | a0001c0001t0004g0021a0001c0001t0004g0065a0001c0001t0004g0096others(6): Show | 10 | HG00738.hp1 HG01261.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1650-2508G>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43817097 | |||||||
| chr2:43817116 | A | G | 121 | a0001c0001t0001g0045a0001c0001t0001g0071a0001c0001t0001g0179others(118): Show | 140 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.1650-2527T>C | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43817116 | |||||||
| chr2:43817327 | A | T | 3 | a0001c0001t0001g0191a0001c0001t0001g0193a0001c0001t0001g0228 | 3 | HG02155.hp1 NA18945.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.1649+2588T>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43817327 | |||||||
| chr2:43817454 | C | T | 1 | a0001c0001t0001g0176 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1649+2461G>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43817454 | |||||||
| chr2:43817485 | C | T | 8 | a0001c0001t0004g0021a0001c0001t0004g0096a0001c0001t0004g0149others(5): Show | 9 | HG00738.hp1 HG02572.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.1649+2430G>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43817485 | |||||||
| chr2:43817541 | C | A | 101 | a0001c0001t0001g0008a0001c0001t0001g0071a0001c0001t0003g0011others(98): Show | 119 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.1649+2374G>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43817541 | |||||||
| chr2:43817551 | A | G | 4 | a0002c0002t0002g0127a0002c0002t0002g0128a0002c0002t0002g0154others(1): Show | 4 | HG02717.hp2 HG02886.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1649+2364T>C | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43817551 | |||||||
| chr2:43817635 | C | T | 1 | a0001c0001t0003g0155 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1649+2280G>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43817635 | |||||||
| chr2:43817636 | G | A | 2 | a0001c0001t0004g0065a0001c0001t0004g0255 | 2 | HG01261.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.1649+2279C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43817636 | |||||||
| chr2:43817638 | G | A | 1 | a0002c0002t0002g0209 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1649+2277C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43817638 | |||||||
| chr2:43817647 | C | T | 10 | a0001c0001t0004g0021a0001c0001t0004g0065a0001c0001t0004g0096others(7): Show | 11 | HG00738.hp1 HG01261.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1649+2268G>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43817647 | |||||||
| chr2:43817685 | A | G | 14 | a0001c0001t0004g0021a0001c0001t0004g0065a0001c0001t0004g0096others(11): Show | 15 | HG00642.hp2 HG00738.hp1 HG01099.hp1 others(12): Show |
intron_variant | MODIFIER | c.1649+2230T>C | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43817685 | |||||||
| chr2:43817700 | A | G | 31 | a0001c0001t0001g0071a0001c0001t0010g0037a0002c0002t0002g0002others(28): Show | 39 | HG00438.hp1 HG00733.hp2 HG01081.hp1 others(36): Show |
intron_variant | MODIFIER | c.1649+2215T>C | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43817700 | |||||||
| chr2:43817728 | G | A | 6 | a0001c0001t0001g0152a0001c0001t0001g0159a0001c0001t0001g0163others(3): Show | 6 | HG01346.hp2 HG02145.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.1649+2187C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43817728 | |||||||
| chr2:43817746 | C | A | 19 | a0001c0001t0001g0045a0001c0001t0001g0179a0001c0001t0001g0215others(16): Show | 21 | HG00099.hp1 HG00597.hp1 HG00673.hp1 others(18): Show |
intron_variant | MODIFIER | c.1649+2169G>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43817746 | |||||||
| chr2:43817757 | A | G | 1 | a0001c0001t0003g0126 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1649+2158T>C | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43817757 | |||||||
| chr2:43817770 | T | C | 16 | a0001c0001t0003g0126a0001c0001t0004g0021a0001c0001t0004g0065others(13): Show | 17 | HG00642.hp2 HG00738.hp1 HG01099.hp1 others(14): Show |
intron_variant | MODIFIER | c.1649+2145A>G | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43817770 | |||||||
| chr2:43817791 | T | A | 19 | a0001c0001t0003g0011a0001c0001t0003g0067a0001c0001t0003g0072others(16): Show | 21 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(18): Show |
intron_variant | MODIFIER | c.1649+2124A>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43817791 | |||||||
| chr2:43817866 | C | T | 19 | a0001c0001t0001g0045a0001c0001t0001g0179a0001c0001t0001g0215others(16): Show | 21 | HG00099.hp1 HG00597.hp1 HG00673.hp1 others(18): Show |
intron_variant | MODIFIER | c.1649+2049G>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43817866 | |||||||
| chr2:43817996 | C | T | 2 | a0001c0001t0005g0232a0001c0001t0005g0233 | 2 | HG01074.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.1649+1919G>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43817996 | |||||||
| chr2:43818145 | A | T | 4 | a0002c0002t0002g0143a0002c0002t0002g0146a0002c0002t0002g0153others(1): Show | 4 | HG02559.hp1 HG02922.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1649+1770T>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43818145 | |||||||
| chr2:43818260 | A | G | 1 | a0001c0001t0001g0047 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1649+1655T>C | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43818260 | |||||||
| chr2:43818263 | G | A | 20 | a0001c0001t0001g0045a0001c0001t0001g0179a0001c0001t0001g0215others(17): Show | 22 | HG00099.hp1 HG00597.hp1 HG00673.hp1 others(19): Show |
intron_variant | MODIFIER | c.1649+1652C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43818263 | |||||||
| chr2:43818273 | A | G | 1 | a0001c0001t0001g0119 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1649+1642T>C | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43818273 | |||||||
| chr2:43818423 | G | A | 1 | a0001c0001t0001g0116 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1649+1492C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43818423 | |||||||
| chr2:43818485 | G | C | 1 | a0002c0002t0002g0030 | 2 | HG01081.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.1649+1430C>G | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43818485 | |||||||
| chr2:43818487 | G | A | 3 | a0001c0001t0001g0044a0001c0001t0001g0112a0001c0001t0001g0119 | 3 | NA18942.hp2 NA18959.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.1649+1428C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43818487 | |||||||
| chr2:43818607 | A | G | 2 | a0001c0001t0003g0027a0001c0001t0003g0226 | 3 | HG02723.hp1 HG02723.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1649+1308T>C | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43818607 | |||||||
| chr2:43818708 | G | C | 1 | a0012c0014t0002g0162 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1649+1207C>G | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43818708 | |||||||
| chr2:43818793 | G | A | 30 | a0001c0001t0003g0011a0001c0001t0003g0027a0001c0001t0003g0066others(27): Show | 37 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(34): Show |
intron_variant | MODIFIER | c.1649+1122C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43818793 | |||||||
| chr2:43818828 | G | A | 1 | a0001c0001t0003g0231 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1649+1087C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43818828 | |||||||
| chr2:43818933 | G | A | 1 | a0001c0001t0003g0226 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1649+982C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43818933 | |||||||
| chr2:43818935 | A | G | 1 | a0001c0001t0001g0236 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1649+980T>C | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43818935 | |||||||
| chr2:43819087 | C | A | 23 | a0001c0001t0003g0011a0001c0001t0003g0027a0001c0001t0003g0066others(20): Show | 26 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(23): Show |
intron_variant | MODIFIER | c.1649+828G>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43819087 | |||||||
| chr2:43819179 | G | A | 3 | a0001c0001t0007g0225a0001c0001t0011g0259a0001c0001t0011g0260 | 3 | HG03490.hp2 HG03704.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.1649+736C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43819179 | |||||||
| chr2:43819446 | T | C | 87 | a0001c0001t0001g0008a0001c0001t0001g0071a0001c0001t0003g0011others(84): Show | 100 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.1649+469A>G | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43819446 | |||||||
| chr2:43819481 | CT | C | 58 | a0001c0001t0001g0008a0001c0001t0001g0135a0001c0001t0003g0011others(55): Show | 64 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(61): Show |
intron_variant | MODIFIER | c.1649+433delA | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43819481 | |||||||
| chr2:43819530 | T | G | 3 | a0002c0002t0002g0034a0002c0002t0002g0185a0004c0004t0002g0252 | 4 | HG01975.hp1 NA18962.hp1 NA18977.hp2 others(1): Show |
intron_variant | MODIFIER | c.1649+385A>C | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43819530 | |||||||
| chr2:43819630 | A | G | 1 | a0002c0002t0002g0153 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1649+285T>C | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43819630 | |||||||
| chr2:43819634 | G | A | 1 | a0001c0001t0001g0029 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1649+281C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43819634 | |||||||
| chr2:43819698 | G | A | 3 | a0002c0002t0002g0035a0002c0002t0002g0187a0002c0002t0002g0209 | 4 | HG02155.hp2 NA18952.hp1 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.1649+217C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43819698 | |||||||
| chr2:43819773 | C | T | 1 | a0001c0001t0010g0037 | 2 | HG01109.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1649+142G>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 11/12 | chr2 | 43819773 | |||||||
| chr2:43820208 | T | A | 7 | a0002c0002t0002g0138a0002c0002t0002g0181a0002c0002t0002g0189others(4): Show | 7 | HG00741.hp2 HG01192.hp1 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.1464-108A>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 10/12 | chr2 | 43820208 | |||||||
| chr2:43820283 | A | G | 4 | a0001c0001t0007g0108a0001c0001t0007g0150a0001c0001t0007g0156others(1): Show | 4 | HG02055.hp2 HG02109.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1464-183T>C | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 10/12 | chr2 | 43820283 | |||||||
| chr2:43820319 | C | T | 4 | a0002c0002t0002g0103a0002c0002t0002g0104a0002c0002t0002g0164others(1): Show | 4 | HG00642.hp2 HG01099.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.1464-219G>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 10/12 | chr2 | 43820319 | |||||||
| chr2:43820376 | A | G | 1 | a0001c0001t0001g0057 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1464-276T>C | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 10/12 | chr2 | 43820376 | |||||||
| chr2:43820391 | C | T | 93 | a0001c0001t0001g0008a0001c0001t0001g0071a0001c0001t0003g0011others(90): Show | 108 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.1464-291G>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 10/12 | chr2 | 43820391 | |||||||
| chr2:43820469 | TAATGTTA | T | 3 | a0002c0002t0002g0034a0002c0002t0002g0185a0004c0004t0002g0252 | 4 | HG01975.hp1 NA18962.hp1 NA18977.hp2 others(1): Show |
intron_variant | MODIFIER | c.1464-376_1464-370d others(9): Show |
ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 10/12 | chr2 | 43820469 | |||||||
| chr2:43820512 | C | G | 1 | a0001c0001t0001g0215 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1464-412G>C | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 10/12 | chr2 | 43820512 | |||||||
| chr2:43820551 | G | A | 1 | a0001c0001t0001g0200 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1464-451C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 10/12 | chr2 | 43820551 | |||||||
| chr2:43820616 | T | A | 1 | a0001c0001t0001g0069 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1464-516A>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 10/12 | chr2 | 43820616 | |||||||
| chr2:43820789 | G | A | 4 | a0002c0002t0002g0103a0002c0002t0002g0104a0002c0002t0002g0164others(1): Show | 4 | HG00642.hp2 HG01099.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.1464-689C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 10/12 | chr2 | 43820789 | |||||||
| chr2:43820813 | C | T | 1 | a0007c0007t0001g0256 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1464-713G>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 10/12 | chr2 | 43820813 | |||||||
| chr2:43820835 | G | A | 1 | a0001c0001t0001g0071 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1464-735C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 10/12 | chr2 | 43820835 | |||||||
| chr2:43820838 | G | C | 2 | a0002c0002t0002g0060a0002c0002t0002g0061 | 2 | NA18964.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.1464-738C>G | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 10/12 | chr2 | 43820838 | |||||||
| chr2:43820842 | T | A | 1 | a0002c0002t0002g0146 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1464-742A>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 10/12 | chr2 | 43820842 | |||||||
| chr2:43821005 | CTT | C | 4 | a0002c0002t0002g0103a0002c0002t0002g0104a0002c0002t0002g0164others(1): Show | 4 | HG00642.hp2 HG01099.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.1464-907_1464-906d others(4): Show |
ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 10/12 | chr2 | 43821005 | |||||||
| chr2:43821056 | T | A | 1 | a0010c0018t0004g0258 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1464-956A>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 10/12 | chr2 | 43821056 | |||||||
| chr2:43821111 | G | A | 1 | a0001c0001t0001g0054 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1464-1011C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 10/12 | chr2 | 43821111 | |||||||
| chr2:43821203 | A | G | 3 | a0001c0001t0001g0057a0001c0001t0001g0129a0001c0001t0001g0221 | 3 | HG01123.hp1 HG02602.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.1464-1103T>C | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 10/12 | chr2 | 43821203 | |||||||
| chr2:43821207 | C | T | 24 | a0001c0001t0001g0071a0002c0002t0002g0002a0002c0002t0002g0030others(21): Show | 31 | HG00733.hp2 HG01081.hp1 HG01168.hp1 others(28): Show |
intron_variant | MODIFIER | c.1464-1107G>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 10/12 | chr2 | 43821207 | |||||||
| chr2:43821407 | C | T | 1 | a0001c0001t0001g0094 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1464-1307G>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 10/12 | chr2 | 43821407 | |||||||
| chr2:43821447 | G | A | 6 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0183others(3): Show | 8 | HG02257.hp1 HG02280.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1464-1347C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 10/12 | chr2 | 43821447 | |||||||
| chr2:43821452 | C | T | 14 | a0001c0001t0003g0155a0001c0001t0003g0172a0001c0001t0004g0021others(11): Show | 16 | HG00738.hp1 HG01261.hp2 HG01515.hp1 others(13): Show |
intron_variant | MODIFIER | c.1463+1345G>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 10/12 | chr2 | 43821452 | |||||||
| chr2:43821476 | G | A | 3 | a0001c0001t0001g0152a0001c0001t0001g0163a0003c0003t0001g0248 | 3 | HG01346.hp2 HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1463+1321C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 10/12 | chr2 | 43821476 | |||||||
| chr2:43821531 | C | G | 11 | a0002c0002t0002g0046a0002c0002t0002g0138a0002c0002t0002g0146others(8): Show | 11 | HG00741.hp2 HG01192.hp1 HG01981.hp1 others(8): Show |
intron_variant | MODIFIER | c.1463+1266G>C | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 10/12 | chr2 | 43821531 | |||||||
| chr2:43821541 | T | C | 5 | a0001c0001t0007g0227a0002c0002t0002g0026a0002c0002t0002g0048others(2): Show | 6 | HG02622.hp1 HG02976.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1463+1256A>G | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 10/12 | chr2 | 43821541 | |||||||
| chr2:43821787 | C | G | 4 | a0002c0002t0002g0026a0002c0002t0002g0048a0002c0002t0002g0083others(1): Show | 5 | HG02622.hp1 HG02976.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1463+1010G>C | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 10/12 | chr2 | 43821787 | |||||||
| chr2:43821981 | G | A | 207 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(204): Show | 262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.1463+816C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 10/12 | chr2 | 43821981 | |||||||
| chr2:43822390 | C | G | 1 | a0004c0004t0002g0238 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1463+407G>C | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 10/12 | chr2 | 43822390 | |||||||
| chr2:43822476 | A | AGCC | 12 | a0001c0001t0001g0052a0001c0001t0001g0068a0001c0001t0001g0089others(9): Show | 13 | HG01175.hp1 HG01175.hp2 HG01516.hp2 others(10): Show |
intron_variant | MODIFIER | c.1463+320_1463+321i others(5): Show |
ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 10/12 | chr2 | 43822476 | |||||||
| chr2:43822476 | AG | A | 11 | a0001c0001t0001g0045a0001c0001t0001g0118a0001c0001t0001g0152others(8): Show | 11 | HG01346.hp1 HG01346.hp2 HG01981.hp1 others(8): Show |
intron_variant | MODIFIER | c.1463+320delC | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 10/12 | chr2 | 43822476 | |||||||
| chr2:43822477 | G | GC | 6 | a0001c0001t0001g0210a0002c0002t0002g0093a0002c0002t0002g0195others(3): Show | 7 | HG01243.hp1 HG01993.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.1463+319_1463+320i others(3): Show |
ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 10/12 | chr2 | 43822477 | |||||||
| chr2:43822477 | G | GCC | 7 | a0001c0001t0001g0114a0001c0001t0003g0064a0001c0001t0003g0231others(4): Show | 7 | HG02886.hp2 HG03139.hp1 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.1463+319_1463+320i others(4): Show |
ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 10/12 | chr2 | 43822477 | |||||||
| chr2:43822477 | G | GCCCCCCC others(3): Show |
1 | a0002c0002t0002g0165 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1463+319_1463+320i others(12): Show |
ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 10/12 | chr2 | 43822477 | |||||||
| chr2:43822477 | G | GCCGC | 6 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0004g0255others(3): Show | 7 | HG00639.hp2 HG01516.hp1 HG01517.hp1 others(4): Show |
intron_variant | MODIFIER | c.1463+319_1463+320i others(6): Show |
ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 10/12 | chr2 | 43822477 | |||||||
| chr2:43822477 | G | GCCGCCC | 2 | a0001c0001t0003g0011a0002c0002t0002g0010 | 4 | HG02896.hp2 HG02897.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.1463+319_1463+320i others(8): Show |
ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 10/12 | chr2 | 43822477 | |||||||
| chr2:43822478 | G | C | 218 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(215): Show | 284 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(281): Show |
intron_variant | MODIFIER | c.1463+319C>G | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 10/12 | chr2 | 43822478 | |||||||
| chr2:43822478 | GC | G | 18 | a0001c0001t0001g0017a0001c0001t0001g0047a0001c0001t0001g0122others(15): Show | 20 | HG00140.hp1 HG00642.hp1 HG00738.hp1 others(17): Show |
intron_variant | MODIFIER | c.1463+318delG | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 10/12 | chr2 | 43822478 | |||||||
| chr2:43822479 | C | A | 1 | a0001c0001t0001g0115 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1463+318G>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 10/12 | chr2 | 43822479 | |||||||
| chr2:43822479 | C | CG | 43 | a0001c0001t0001g0007a0001c0001t0001g0024a0001c0001t0001g0028others(40): Show | 54 | HG00738.hp2 HG01106.hp2 HG01167.hp2 others(51): Show |
intron_variant | MODIFIER | c.1463+317_1463+318i others(3): Show |
ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 10/12 | chr2 | 43822479 | |||||||
| chr2:43822510 | T | G | 7 | a0001c0001t0003g0080a0001c0001t0003g0081a0001c0001t0003g0102others(4): Show | 7 | HG00738.hp2 HG02818.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.1463+287A>C | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 10/12 | chr2 | 43822510 | |||||||
| chr2:43822579 | A | C | 1 | a0001c0001t0001g0221 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1463+218T>G | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 10/12 | chr2 | 43822579 | |||||||
| chr2:43822599 | G | A | 1 | a0001c0001t0001g0047 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1463+198C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 10/12 | chr2 | 43822599 | |||||||
| chr2:43822656 | C | T | 2 | a0001c0001t0001g0003a0001c0001t0001g0086 | 5 | HG00735.hp1 HG01081.hp2 HG01168.hp2 others(2): Show |
intron_variant | MODIFIER | c.1463+141G>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 10/12 | chr2 | 43822656 | |||||||
| chr2:43822733 | C | T | 14 | a0001c0001t0001g0062a0001c0001t0001g0073a0001c0001t0001g0142others(11): Show | 15 | HG00323.hp1 HG00738.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1463+64G>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 10/12 | chr2 | 43822733 | |||||||
| chr2:43822768 | G | A | 1 | a0001c0001t0001g0211 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1463+29C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 10/12 | chr2 | 43822768 | |||||||
| chr2:43823202 | G | A | 2 | a0001c0001t0003g0011a0002c0002t0002g0010 | 4 | HG02896.hp2 HG02897.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.1325-267C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 9/12 | chr2 | 43823202 | |||||||
| chr2:43823415 | C | G | 1 | a0001c0001t0001g0044 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1325-480G>C | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 9/12 | chr2 | 43823415 | |||||||
| chr2:43823432 | T | C | 1 | a0002c0002t0002g0046 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1324+481A>G | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 9/12 | chr2 | 43823432 | |||||||
| chr2:43823526 | G | A | 6 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0003g0226others(3): Show | 7 | HG01109.hp1 HG02257.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.1324+387C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 9/12 | chr2 | 43823526 | |||||||
| chr2:43823548 | C | T | 112 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(109): Show | 154 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(151): Show |
intron_variant | MODIFIER | c.1324+365G>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 9/12 | chr2 | 43823548 | |||||||
| chr2:43823569 | A | C | 1 | a0001c0001t0001g0085 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1324+344T>G | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 9/12 | chr2 | 43823569 | |||||||
| chr2:43823671 | C | G | 8 | a0001c0001t0001g0094a0001c0001t0001g0152a0001c0001t0003g0147others(5): Show | 8 | HG01346.hp2 HG02486.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.1324+242G>C | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 9/12 | chr2 | 43823671 | |||||||
| chr2:43823749 | G | A | 103 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(100): Show | 144 | HG00280.hp2 HG00438.hp1 HG00597.hp1 others(141): Show |
intron_variant | MODIFIER | c.1324+164C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 9/12 | chr2 | 43823749 | |||||||
| chr2:43823823 | C | A | 1 | a0001c0001t0003g0102 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1324+90G>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 9/12 | chr2 | 43823823 | |||||||
| chr2:43823832 | G | A | 6 | a0001c0001t0001g0152a0001c0001t0003g0147a0001c0001t0003g0148others(3): Show | 6 | HG01346.hp2 HG02486.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.1324+81C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 9/12 | chr2 | 43823832 | |||||||
| chr2:43823840 | T | A | 2 | a0002c0002t0002g0036a0002c0002t0002g0223 | 3 | HG00733.hp2 HG01934.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.1324+73A>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 9/12 | chr2 | 43823840 | |||||||
| chr2:43824148 | T | C | 4 | a0006c0005t0002g0009a0006c0005t0008g0043a0006c0005t0008g0049others(1): Show | 5 | HG01884.hp1 HG01884.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1119-30A>G | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 8/12 | chr2 | 43824148 | |||||||
| chr2:43824434 | T | TA | 3 | a0001c0001t0001g0033a0001c0001t0001g0097a0001c0001t0001g0140 | 4 | NA18950.hp2 NA18991.hp1 NA18993.hp2 others(1): Show |
splice_region_variant&intron_variant | LOW | c.905-3dupT | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 7/12 | chr2 | 43824434 | |||||||
| chr2:43824558 | T | A | 1 | a0001c0001t0001g0199 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.905-126A>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 7/12 | chr2 | 43824558 | |||||||
| chr2:43824559 | G | T | 1 | a0001c0001t0001g0199 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.905-127C>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 7/12 | chr2 | 43824559 | |||||||
| chr2:43824560 | C | G | 1 | a0001c0001t0001g0199 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.905-128G>C | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 7/12 | chr2 | 43824560 | |||||||
| chr2:43824751 | A | T | 22 | a0001c0001t0001g0094a0001c0001t0001g0152a0001c0001t0001g0159others(19): Show | 24 | HG01243.hp1 HG01346.hp2 HG01884.hp1 others(21): Show |
intron_variant | MODIFIER | c.904+138T>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 7/12 | chr2 | 43824751 | |||||||
| chr2:43825027 | A | G | 1 | a0001c0001t0001g0191 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.775-9T>C | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 6/12 | chr2 | 43825027 | |||||||
| chr2:43825028 | C | A | 2 | a0001c0001t0003g0231a0002c0002t0002g0005 | 5 | HG02647.hp2 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.775-10G>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 6/12 | chr2 | 43825028 | |||||||
| chr2:43825063 | C | A | 10 | a0001c0001t0001g0094a0001c0001t0001g0152a0001c0001t0001g0230others(7): Show | 10 | HG01346.hp2 HG02486.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.775-45G>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 6/12 | chr2 | 43825063 | |||||||
| chr2:43825064 | G | A | 2 | a0001c0001t0001g0169a0001c0001t0001g0180 | 2 | NA18979.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.775-46C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 6/12 | chr2 | 43825064 | |||||||
| chr2:43825277 | C | T | 12 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0003g0226others(9): Show | 14 | HG00642.hp2 HG01074.hp1 HG01099.hp1 others(11): Show |
intron_variant | MODIFIER | c.775-259G>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 6/12 | chr2 | 43825277 | |||||||
| chr2:43825359 | G | A | 4 | a0001c0001t0001g0212a0001c0001t0003g0226a0001c0001t0007g0227others(1): Show | 5 | HG01109.hp1 HG02486.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.775-341C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 6/12 | chr2 | 43825359 | |||||||
| chr2:43825405 | T | C | 1 | a0001c0001t0001g0193 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.775-387A>G | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 6/12 | chr2 | 43825405 | |||||||
| chr2:43825601 | G | T | 3 | a0002c0002t0002g0181a0002c0002t0002g0189a0002c0002t0002g0190 | 3 | HG03130.hp2 HG03195.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.775-583C>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 6/12 | chr2 | 43825601 | |||||||
| chr2:43825604 | GTTA | G | 19 | a0001c0001t0001g0047a0002c0002t0002g0138a0003c0003t0001g0239others(16): Show | 20 | HG00741.hp2 HG01192.hp1 HG01943.hp2 others(17): Show |
intron_variant | MODIFIER | c.775-589_775-587del others(3): Show |
ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 6/12 | chr2 | 43825604 | |||||||
| chr2:43825607 | A | G | 3 | a0001c0001t0003g0126a0002c0002t0002g0127a0002c0002t0002g0128 | 3 | HG02717.hp1 HG02886.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.775-589T>C | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 6/12 | chr2 | 43825607 | |||||||
| chr2:43825639 | A | C | 20 | a0001c0001t0001g0094a0001c0001t0001g0152a0001c0001t0001g0163others(17): Show | 20 | HG01346.hp2 HG02109.hp2 HG02451.hp1 others(17): Show |
intron_variant | MODIFIER | c.775-621T>G | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 6/12 | chr2 | 43825639 | |||||||
| chr2:43825649 | G | T | 1 | a0001c0001t0003g0145 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.775-631C>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 6/12 | chr2 | 43825649 | |||||||
| chr2:43825694 | C | A | 121 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(118): Show | 161 | HG00099.hp1 HG00438.hp1 HG00597.hp1 others(158): Show |
intron_variant | MODIFIER | c.775-676G>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 6/12 | chr2 | 43825694 | |||||||
| chr2:43825732 | G | A | 1 | a0001c0001t0001g0230 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.774+650C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 6/12 | chr2 | 43825732 | |||||||
| chr2:43825752 | G | A | 1 | a0001c0001t0001g0213 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.774+630C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 6/12 | chr2 | 43825752 | |||||||
| chr2:43825763 | C | T | 1 | a0001c0013t0001g0198 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.774+619G>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 6/12 | chr2 | 43825763 | |||||||
| chr2:43825869 | A | G | 2 | a0003c0003t0001g0248a0003c0003t0006g0038 | 3 | HG03098.hp1 HG03209.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.774+513T>C | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 6/12 | chr2 | 43825869 | |||||||
| chr2:43825951 | G | A | 76 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(73): Show | 108 | HG00099.hp1 HG00438.hp1 HG00597.hp1 others(105): Show |
intron_variant | MODIFIER | c.774+431C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 6/12 | chr2 | 43825951 | |||||||
| chr2:43826106 | G | C | 3 | a0002c0002t0002g0181a0002c0002t0002g0189a0002c0002t0002g0190 | 3 | HG03130.hp2 HG03195.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.774+276C>G | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 6/12 | chr2 | 43826106 | |||||||
| chr2:43826166 | C | CT | 8 | a0001c0001t0001g0214a0001c0001t0001g0215a0001c0001t0001g0230others(5): Show | 9 | HG00099.hp1 HG01361.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.774+215dupA | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 6/12 | chr2 | 43826166 | |||||||
| chr2:43826184 | G | T | 1 | a0002c0002t0002g0100 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.774+198C>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 6/12 | chr2 | 43826184 | |||||||
| chr2:43826216 | A | G | 4 | a0006c0005t0002g0009a0006c0005t0008g0043a0006c0005t0008g0049others(1): Show | 5 | HG01884.hp1 HG01884.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.774+166T>C | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 6/12 | chr2 | 43826216 | |||||||
| chr2:43826309 | A | T | 6 | a0001c0001t0003g0080a0001c0001t0003g0081a0001c0001t0003g0102others(3): Show | 6 | HG00738.hp2 HG02818.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.774+73T>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 6/12 | chr2 | 43826309 | |||||||
| chr2:43826622 | A | G | 1 | a0002c0002t0002g0197 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.635-101T>C | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 5/12 | chr2 | 43826622 | |||||||
| chr2:43826638 | G | A | 1 | a0001c0001t0009g0261 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.635-117C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 5/12 | chr2 | 43826638 | |||||||
| chr2:43826791 | G | A | 1 | a0001c0001t0005g0079 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.635-270C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 5/12 | chr2 | 43826791 | |||||||
| chr2:43826800 | A | G | 1 | a0001c0001t0001g0196 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.635-279T>C | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 5/12 | chr2 | 43826800 | |||||||
| chr2:43826809 | T | C | 4 | a0006c0005t0002g0009a0006c0005t0008g0043a0006c0005t0008g0049others(1): Show | 5 | HG01884.hp1 HG01884.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.635-288A>G | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 5/12 | chr2 | 43826809 | |||||||
| chr2:43826984 | G | A | 84 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(81): Show | 120 | HG00099.hp1 HG00438.hp1 HG00597.hp1 others(117): Show |
intron_variant | MODIFIER | c.635-463C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 5/12 | chr2 | 43826984 | |||||||
| chr2:43826985 | C | T | 1 | a0002c0002t0002g0195 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.635-464G>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 5/12 | chr2 | 43826985 | |||||||
| chr2:43827050 | C | T | 1 | a0001c0001t0001g0051 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.635-529G>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 5/12 | chr2 | 43827050 | |||||||
| chr2:43827052 | C | T | 1 | a0002c0009t0002g0042 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.635-531G>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 5/12 | chr2 | 43827052 | |||||||
| chr2:43827053 | G | A | 1 | a0001c0001t0001g0070 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.635-532C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 5/12 | chr2 | 43827053 | |||||||
| chr2:43827054 | G | A | 6 | a0001c0001t0001g0152a0001c0001t0003g0147a0001c0001t0003g0148others(3): Show | 6 | HG01346.hp2 HG02486.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.635-533C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 5/12 | chr2 | 43827054 | |||||||
| chr2:43827127 | C | G | 1 | a0001c0001t0001g0059 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.635-606G>C | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 5/12 | chr2 | 43827127 | |||||||
| chr2:43827245 | A | C | 1 | a0001c0001t0003g0064 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.635-724T>G | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 5/12 | chr2 | 43827245 | |||||||
| chr2:43827279 | C | T | 2 | a0001c0001t0006g0141a0002c0002t0002g0224 | 2 | HG02055.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.634+704G>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 5/12 | chr2 | 43827279 | |||||||
| chr2:43827298 | C | A | 84 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(81): Show | 120 | HG00099.hp1 HG00438.hp1 HG00597.hp1 others(117): Show |
intron_variant | MODIFIER | c.634+685G>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 5/12 | chr2 | 43827298 | |||||||
| chr2:43827325 | C | CA | 35 | a0001c0001t0001g0045a0001c0001t0001g0094a0001c0001t0001g0101others(32): Show | 38 | HG00099.hp1 HG00609.hp1 HG00609.hp2 others(35): Show |
intron_variant | MODIFIER | c.634+657dupT | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 5/12 | chr2 | 43827325 | |||||||
| chr2:43827325 | C | CAA | 21 | a0001c0001t0001g0047a0001c0001t0001g0071a0002c0002t0002g0138others(18): Show | 22 | HG00741.hp2 HG01192.hp1 HG01943.hp2 others(19): Show |
intron_variant | MODIFIER | c.634+656_634+657dup others(2): Show |
ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 5/12 | chr2 | 43827325 | |||||||
| chr2:43827325 | CA | C | 5 | a0001c0001t0001g0159a0005c0006t0001g0160a0005c0006t0006g0025others(2): Show | 6 | HG01243.hp1 HG02145.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.634+657delT | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 5/12 | chr2 | 43827325 | |||||||
| chr2:43827343 | G | T | 86 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(83): Show | 122 | HG00099.hp1 HG00438.hp1 HG00597.hp1 others(119): Show |
intron_variant | MODIFIER | c.634+640C>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 5/12 | chr2 | 43827343 | |||||||
| chr2:43827345 | G | A | 86 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(83): Show | 122 | HG00099.hp1 HG00438.hp1 HG00597.hp1 others(119): Show |
intron_variant | MODIFIER | c.634+638C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 5/12 | chr2 | 43827345 | |||||||
| chr2:43827379 | C | T | 1 | a0002c0002t0002g0060 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.634+604G>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 5/12 | chr2 | 43827379 | |||||||
| chr2:43827400 | T | C | 2 | a0001c0001t0001g0230a0002c0009t0002g0042 | 2 | HG02717.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.634+583A>G | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 5/12 | chr2 | 43827400 | |||||||
| chr2:43827617 | A | G | 2 | a0001c0001t0003g0231a0002c0002t0002g0005 | 5 | HG02647.hp2 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.634+366T>C | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 5/12 | chr2 | 43827617 | |||||||
| chr2:43827655 | C | G | 1 | a0001c0001t0001g0194 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.634+328G>C | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 5/12 | chr2 | 43827655 | |||||||
| chr2:43827799 | C | T | 1 | a0001c0001t0001g0174 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.634+184G>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 5/12 | chr2 | 43827799 | |||||||
| chr2:43827830 | A | G | 2 | a0001c0001t0001g0230a0002c0009t0002g0042 | 2 | HG02717.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.634+153T>C | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 5/12 | chr2 | 43827830 | |||||||
| chr2:43827852 | G | A | 18 | a0002c0002t0002g0138a0003c0003t0001g0239a0003c0003t0001g0240others(15): Show | 19 | HG00741.hp2 HG01192.hp1 HG01943.hp2 others(16): Show |
intron_variant | MODIFIER | c.634+131C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 5/12 | chr2 | 43827852 | |||||||
| chr2:43827902 | G | A | 1 | a0001c0001t0001g0133 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.634+81C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 5/12 | chr2 | 43827902 | |||||||
| chr2:43828248 | C | T | 32 | a0001c0001t0001g0152a0001c0001t0001g0163a0001c0001t0001g0236others(29): Show | 35 | HG00642.hp2 HG01074.hp1 HG01099.hp1 others(32): Show |
intron_variant | MODIFIER | c.502-133G>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 4/12 | chr2 | 43828248 | |||||||
| chr2:43828307 | G | A | 94 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(91): Show | 134 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.502-192C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 4/12 | chr2 | 43828307 | |||||||
| chr2:43828371 | C | T | 19 | a0001c0001t0001g0047a0002c0002t0002g0138a0003c0003t0001g0239others(16): Show | 20 | HG00741.hp2 HG01192.hp1 HG01943.hp2 others(17): Show |
intron_variant | MODIFIER | c.502-256G>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 4/12 | chr2 | 43828371 | |||||||
| chr2:43828388 | T | C | 153 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(150): Show | 198 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(195): Show |
intron_variant | MODIFIER | c.502-273A>G | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 4/12 | chr2 | 43828388 | |||||||
| chr2:43828404 | G | A | 2 | a0001c0001t0003g0226a0001c0001t0010g0037 | 3 | HG01109.hp1 HG02723.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.502-289C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 4/12 | chr2 | 43828404 | |||||||
| chr2:43828472 | C | CA | 26 | a0001c0001t0001g0098a0001c0001t0001g0117a0001c0001t0003g0072others(23): Show | 28 | HG00738.hp1 HG00741.hp2 HG01192.hp1 others(25): Show |
intron_variant | MODIFIER | c.502-358dupT | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 4/12 | chr2 | 43828472 | |||||||
| chr2:43828472 | CA | C | 13 | a0001c0001t0001g0152a0001c0001t0001g0169a0001c0001t0001g0230others(10): Show | 14 | HG01243.hp1 HG01346.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.502-358delT | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 4/12 | chr2 | 43828472 | |||||||
| chr2:43828472 | CAA | C | 94 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(91): Show | 134 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.502-359_502-358del others(2): Show |
ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 4/12 | chr2 | 43828472 | |||||||
| chr2:43828472 | CAAAAAAA | C | 8 | a0001c0001t0001g0057a0001c0001t0001g0236a0001c0001t0001g0237others(5): Show | 9 | HG01074.hp1 HG01109.hp1 HG01123.hp1 others(6): Show |
intron_variant | MODIFIER | c.502-364_502-358del others(7): Show |
ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 4/12 | chr2 | 43828472 | |||||||
| chr2:43828472 | CAAAAAAA others(1): Show |
C | 5 | a0001c0001t0005g0232a0002c0002t0002g0026a0002c0002t0002g0164others(2): Show | 6 | HG00642.hp2 HG01099.hp1 HG01099.hp2 others(3): Show |
intron_variant | MODIFIER | c.502-365_502-358del others(8): Show |
ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 4/12 | chr2 | 43828472 | |||||||
| chr2:43828490 | A | G | 3 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193 | 3 | NA18945.hp1 NA18973.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.502-375T>C | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 4/12 | chr2 | 43828490 | |||||||
| chr2:43828510 | A | C | 137 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(134): Show | 183 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(180): Show |
intron_variant | MODIFIER | c.502-395T>G | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 4/12 | chr2 | 43828510 | |||||||
| chr2:43828592 | G | A | 1 | a0002c0002t0002g0124 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.502-477C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 4/12 | chr2 | 43828592 | |||||||
| chr2:43828731 | C | T | 1 | a0004c0004t0002g0253 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.502-616G>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 4/12 | chr2 | 43828731 | |||||||
| chr2:43828732 | G | T | 1 | a0002c0002t0002g0127 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.502-617C>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 4/12 | chr2 | 43828732 | |||||||
| chr2:43828738 | G | C | 2 | a0002c0002t0002g0036a0002c0002t0002g0223 | 3 | HG00733.hp2 HG01934.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.502-623C>G | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 4/12 | chr2 | 43828738 | |||||||
| chr2:43828783 | C | T | 21 | a0001c0001t0001g0047a0001c0001t0001g0230a0002c0002t0002g0138others(18): Show | 22 | HG00741.hp2 HG01192.hp1 HG01943.hp2 others(19): Show |
intron_variant | MODIFIER | c.502-668G>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 4/12 | chr2 | 43828783 | |||||||
| chr2:43828858 | C | CG | 135 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(132): Show | 179 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(176): Show |
intron_variant | MODIFIER | c.502-744dupC | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 4/12 | chr2 | 43828858 | |||||||
| chr2:43828870 | C | T | 42 | a0001c0001t0001g0152a0001c0001t0001g0159a0001c0001t0001g0163others(39): Show | 46 | HG00642.hp2 HG01074.hp1 HG01099.hp1 others(43): Show |
intron_variant | MODIFIER | c.502-755G>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 4/12 | chr2 | 43828870 | |||||||
| chr2:43828885 | A | G | 4 | a0001c0001t0005g0076a0001c0001t0005g0077a0001c0001t0005g0079others(1): Show | 4 | HG01891.hp1 HG02622.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.502-770T>C | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 4/12 | chr2 | 43828885 | |||||||
| chr2:43828910 | AG | A | 101 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(98): Show | 142 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(139): Show |
intron_variant | MODIFIER | c.502-796delC | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 4/12 | chr2 | 43828910 | |||||||
| chr2:43828952 | G | A | 2 | a0001c0001t0003g0231a0002c0002t0002g0005 | 5 | HG02647.hp2 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.502-837C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 4/12 | chr2 | 43828952 | |||||||
| chr2:43828960 | G | A | 2 | a0001c0001t0001g0219a0001c0001t0001g0220 | 2 | HG00673.hp1 HG02015.hp1 |
intron_variant | MODIFIER | c.502-845C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 4/12 | chr2 | 43828960 | |||||||
| chr2:43828970 | A | T | 1 | a0001c0001t0001g0230 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.502-855T>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 4/12 | chr2 | 43828970 | |||||||
| chr2:43828972 | AT | A | 3 | a0001c0001t0001g0062a0001c0001t0001g0073a0005c0006t0001g0160 | 3 | HG02083.hp2 HG03225.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.502-858delA | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 4/12 | chr2 | 43828972 | |||||||
| chr2:43828973 | T | A | 102 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(99): Show | 144 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.502-858A>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 4/12 | chr2 | 43828973 | |||||||
| chr2:43828976 | T | A | 1 | a0005c0006t0001g0160 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.502-861A>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 4/12 | chr2 | 43828976 | |||||||
| chr2:43828991 | CAAATA | C | 5 | a0001c0001t0003g0011a0002c0002t0002g0010a0002c0002t0002g0048others(2): Show | 7 | HG02559.hp1 HG02896.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.502-881_502-877del others(5): Show |
ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 4/12 | chr2 | 43828991 | |||||||
| chr2:43829009 | A | T | 19 | a0001c0001t0001g0047a0002c0002t0002g0138a0003c0003t0001g0239others(16): Show | 20 | HG00741.hp2 HG01192.hp1 HG01943.hp2 others(17): Show |
intron_variant | MODIFIER | c.502-894T>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 4/12 | chr2 | 43829009 | |||||||
| chr2:43829118 | C | A | 1 | a0001c0001t0001g0098 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.502-1003G>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 4/12 | chr2 | 43829118 | |||||||
| chr2:43829183 | T | C | 137 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(134): Show | 182 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(179): Show |
intron_variant | MODIFIER | c.502-1068A>G | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 4/12 | chr2 | 43829183 | |||||||
| chr2:43829184 | T | C | 1 | a0001c0001t0001g0099 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.502-1069A>G | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 4/12 | chr2 | 43829184 | |||||||
| chr2:43829240 | C | T | 13 | a0001c0001t0003g0080a0001c0001t0003g0081a0001c0001t0003g0102others(10): Show | 13 | HG00738.hp2 HG01243.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.502-1125G>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 4/12 | chr2 | 43829240 | |||||||
| chr2:43829305 | C | T | 137 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(134): Show | 182 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(179): Show |
intron_variant | MODIFIER | c.502-1190G>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 4/12 | chr2 | 43829305 | |||||||
| chr2:43829350 | A | C | 1 | a0001c0001t0001g0230 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.502-1235T>G | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 4/12 | chr2 | 43829350 | |||||||
| chr2:43829402 | A | G | 108 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(105): Show | 151 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.502-1287T>C | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 4/12 | chr2 | 43829402 | |||||||
| chr2:43829451 | G | C | 160 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(157): Show | 208 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(205): Show |
intron_variant | MODIFIER | c.502-1336C>G | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 4/12 | chr2 | 43829451 | |||||||
| chr2:43829539 | T | C | 137 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(134): Show | 182 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(179): Show |
intron_variant | MODIFIER | c.502-1424A>G | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 4/12 | chr2 | 43829539 | |||||||
| chr2:43829661 | A | T | 137 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(134): Show | 182 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(179): Show |
intron_variant | MODIFIER | c.502-1546T>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 4/12 | chr2 | 43829661 | |||||||
| chr2:43829674 | CA | C | 6 | a0001c0001t0001g0152a0001c0001t0003g0147a0001c0001t0003g0148others(3): Show | 6 | HG01346.hp2 HG02486.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.502-1560delT | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 4/12 | chr2 | 43829674 | |||||||
| chr2:43829717 | A | G | 137 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(134): Show | 182 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(179): Show |
intron_variant | MODIFIER | c.502-1602T>C | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 4/12 | chr2 | 43829717 | |||||||
| chr2:43829843 | G | T | 2 | a0001c0001t0004g0170a0001c0010t0004g0186 | 2 | HG02132.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.502-1728C>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 4/12 | chr2 | 43829843 | |||||||
| chr2:43829854 | T | C | 31 | a0001c0001t0001g0152a0001c0001t0001g0163a0001c0001t0001g0236others(28): Show | 34 | HG00642.hp2 HG01074.hp1 HG01099.hp1 others(31): Show |
intron_variant | MODIFIER | c.502-1739A>G | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 4/12 | chr2 | 43829854 | |||||||
| chr2:43829883 | C | T | 1 | a0001c0001t0001g0174 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.502-1768G>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 4/12 | chr2 | 43829883 | |||||||
| chr2:43829887 | C | T | 15 | a0001c0001t0001g0152a0001c0001t0001g0163a0001c0001t0003g0145others(12): Show | 15 | HG01346.hp2 HG02109.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.502-1772G>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 4/12 | chr2 | 43829887 | |||||||
| chr2:43829888 | C | T | 1 | a0001c0001t0001g0075 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.502-1773G>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 4/12 | chr2 | 43829888 | |||||||
| chr2:43829891 | A | G | 102 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(99): Show | 144 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.502-1776T>C | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 4/12 | chr2 | 43829891 | |||||||
| chr2:43829963 | G | A | 155 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(152): Show | 201 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(198): Show |
intron_variant | MODIFIER | c.501+1806C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 4/12 | chr2 | 43829963 | |||||||
| chr2:43830079 | G | A | 96 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(93): Show | 137 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(134): Show |
intron_variant | MODIFIER | c.501+1690C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 4/12 | chr2 | 43830079 | |||||||
| chr2:43830270 | C | G | 31 | a0001c0001t0001g0152a0001c0001t0001g0163a0001c0001t0001g0236others(28): Show | 34 | HG00642.hp2 HG01074.hp1 HG01099.hp1 others(31): Show |
intron_variant | MODIFIER | c.501+1499G>C | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 4/12 | chr2 | 43830270 | |||||||
| chr2:43830431 | A | C | 21 | a0001c0001t0003g0126a0002c0002t0002g0127a0002c0002t0002g0128others(18): Show | 22 | HG00741.hp2 HG01192.hp1 HG01943.hp2 others(19): Show |
intron_variant | MODIFIER | c.501+1338T>G | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 4/12 | chr2 | 43830431 | |||||||
| chr2:43830615 | G | T | 1 | a0001c0001t0001g0032 | 2 | NA18993.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.501+1154C>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 4/12 | chr2 | 43830615 | |||||||
| chr2:43830624 | C | T | 1 | a0001c0001t0001g0032 | 2 | NA18993.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.501+1145G>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 4/12 | chr2 | 43830624 | |||||||
| chr2:43830625 | G | A | 1 | a0002c0002t0002g0100 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.501+1144C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 4/12 | chr2 | 43830625 | |||||||
| chr2:43830686 | TCTC | T | 18 | a0002c0002t0002g0138a0003c0003t0001g0239a0003c0003t0001g0240others(15): Show | 19 | HG00741.hp2 HG01192.hp1 HG01943.hp2 others(16): Show |
intron_variant | MODIFIER | c.501+1080_501+1082d others(5): Show |
ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 4/12 | chr2 | 43830686 | |||||||
| chr2:43830738 | T | C | 37 | a0001c0001t0001g0152a0001c0001t0001g0159a0001c0001t0001g0163others(34): Show | 41 | HG00642.hp2 HG01074.hp1 HG01099.hp1 others(38): Show |
intron_variant | MODIFIER | c.501+1031A>G | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 4/12 | chr2 | 43830738 | |||||||
| chr2:43830928 | A | G | 96 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(93): Show | 137 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(134): Show |
intron_variant | MODIFIER | c.501+841T>C | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 4/12 | chr2 | 43830928 | |||||||
| chr2:43830955 | A | G | 3 | a0002c0002t0002g0181a0002c0002t0002g0189a0002c0002t0002g0190 | 3 | HG03130.hp2 HG03195.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.501+814T>C | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 4/12 | chr2 | 43830955 | |||||||
| chr2:43830980 | A | G | 3 | a0001c0001t0001g0016a0001c0001t0001g0074a0002c0002t0002g0125 | 4 | HG01891.hp2 HG02698.hp1 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.501+789T>C | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 4/12 | chr2 | 43830980 | |||||||
| chr2:43831062 | G | A | 22 | a0001c0001t0001g0047a0001c0001t0003g0126a0002c0002t0002g0127others(19): Show | 23 | HG00741.hp2 HG01192.hp1 HG01943.hp2 others(20): Show |
intron_variant | MODIFIER | c.501+707C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 4/12 | chr2 | 43831062 | |||||||
| chr2:43831080 | G | T | 2 | a0002c0002t0002g0127a0002c0002t0002g0128 | 2 | HG02886.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.501+689C>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 4/12 | chr2 | 43831080 | |||||||
| chr2:43831092 | A | G | 1 | a0001c0001t0001g0230 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.501+677T>C | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 4/12 | chr2 | 43831092 | |||||||
| chr2:43831234 | G | A | 1 | a0001c0001t0001g0101 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.501+535C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 4/12 | chr2 | 43831234 | |||||||
| chr2:43831331 | T | C | 134 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(131): Show | 179 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(176): Show |
intron_variant | MODIFIER | c.501+438A>G | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 4/12 | chr2 | 43831331 | |||||||
| chr2:43831369 | C | T | 3 | a0001c0001t0003g0011a0002c0002t0002g0010a0002c0002t0002g0048 | 5 | HG02896.hp2 HG02897.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.501+400G>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 4/12 | chr2 | 43831369 | |||||||
| chr2:43831439 | C | G | 1 | a0001c0001t0001g0219 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.501+330G>C | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 4/12 | chr2 | 43831439 | |||||||
| chr2:43831599 | C | T | 1 | a0001c0001t0001g0188 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.501+170G>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 4/12 | chr2 | 43831599 | |||||||
| chr2:43831628 | G | A | 2 | a0001c0001t0001g0159a0005c0006t0001g0160 | 2 | HG02145.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.501+141C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 4/12 | chr2 | 43831628 | |||||||
| chr2:43831700 | A | G | 1 | a0002c0002t0002g0187 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.501+69T>C | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 4/12 | chr2 | 43831700 | |||||||
| chr2:43831758 | G | T | 1 | a0001c0001t0001g0230 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.501+11C>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 4/12 | chr2 | 43831758 | |||||||
| chr2:43831906 | G | A | 1 | a0001c0001t0001g0159 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.403-39C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 3/12 | chr2 | 43831906 | |||||||
| chr2:43831920 | G | T | 1 | a0002c0002t0002g0223 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.402+27C>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 3/12 | chr2 | 43831920 | |||||||
| chr2:43832277 | C | A | 1 | a0002c0009t0002g0042 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.266-194G>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43832277 | |||||||
| chr2:43832288 | G | T | 2 | a0003c0003t0001g0239a0004c0004t0002g0238 | 2 | HG02818.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.266-205C>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43832288 | |||||||
| chr2:43832299 | G | A | 10 | a0001c0001t0001g0159a0001c0001t0001g0230a0001c0001t0003g0145others(7): Show | 11 | HG01243.hp1 HG02145.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.266-216C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43832299 | |||||||
| chr2:43832355 | G | A | 1 | a0001c0001t0001g0218 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.266-272C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43832355 | |||||||
| chr2:43832964 | T | C | 134 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(131): Show | 181 | HG00099.hp1 HG00280.hp2 HG00597.hp1 others(178): Show |
intron_variant | MODIFIER | c.266-881A>G | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43832964 | |||||||
| chr2:43832982 | G | A | 2 | a0003c0003t0001g0248a0003c0003t0006g0038 | 3 | HG03098.hp1 HG03209.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.266-899C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43832982 | |||||||
| chr2:43833090 | G | A | 6 | a0001c0001t0001g0008a0001c0001t0001g0159a0002c0002t0002g0136others(3): Show | 7 | HG01192.hp1 HG02145.hp2 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.266-1007C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43833090 | |||||||
| chr2:43833363 | A | ATAT | 36 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0068others(33): Show | 41 | HG00323.hp1 HG00673.hp2 HG00733.hp2 others(38): Show |
intron_variant | MODIFIER | c.266-1283_266-1281d others(5): Show |
ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43833363 | |||||||
| chr2:43833363 | A | ATATTAT | 14 | a0001c0001t0001g0012a0001c0001t0001g0056a0001c0001t0001g0062others(11): Show | 16 | HG00438.hp2 HG01070.hp2 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.266-1286_266-1281d others(8): Show |
ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43833363 | |||||||
| chr2:43833363 | A | ATATTATT others(2): Show |
10 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0001g0053others(7): Show | 11 | HG00099.hp2 HG00741.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.266-1289_266-1281d others(11): Show |
ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43833363 | |||||||
| chr2:43833363 | ATAT | A | 107 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(104): Show | 148 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(145): Show |
intron_variant | MODIFIER | c.266-1283_266-1281d others(5): Show |
ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43833363 | |||||||
| chr2:43833363 | ATATTAT | A | 17 | a0001c0001t0001g0047a0001c0001t0001g0118a0001c0001t0001g0119others(14): Show | 18 | HG00735.hp2 HG00741.hp2 HG01978.hp2 others(15): Show |
intron_variant | MODIFIER | c.266-1286_266-1281d others(8): Show |
ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43833363 | |||||||
| chr2:43833363 | ATATTATT others(2): Show |
A | 5 | a0003c0003t0001g0249a0003c0003t0001g0250a0003c0003t0003g0251others(2): Show | 5 | HG00438.hp1 HG01943.hp2 HG01975.hp1 others(2): Show |
intron_variant | MODIFIER | c.266-1289_266-1281d others(11): Show |
ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43833363 | |||||||
| chr2:43833363 | ATATTATT others(5): Show |
A | 1 | a0001c0001t0001g0230 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.266-1292_266-1281d others(14): Show |
ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43833363 | |||||||
| chr2:43833363 | ATATTATT others(17): Show |
A | 2 | a0001c0001t0003g0231a0002c0002t0002g0005 | 5 | HG02647.hp2 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.266-1304_266-1281d others(26): Show |
ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43833363 | |||||||
| chr2:43833452 | G | C | 1 | a0001c0001t0001g0044 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.266-1369C>G | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43833452 | |||||||
| chr2:43833469 | A | C | 4 | a0002c0002t0002g0026a0002c0002t0002g0164a0002c0002t0002g0165others(1): Show | 5 | HG00642.hp2 HG01099.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.266-1386T>G | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43833469 | |||||||
| chr2:43833531 | G | T | 134 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(131): Show | 181 | HG00099.hp1 HG00280.hp2 HG00597.hp1 others(178): Show |
intron_variant | MODIFIER | c.266-1448C>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43833531 | |||||||
| chr2:43833693 | T | C | 96 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(93): Show | 136 | HG00099.hp1 HG00280.hp2 HG00597.hp1 others(133): Show |
intron_variant | MODIFIER | c.266-1610A>G | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43833693 | |||||||
| chr2:43833710 | A | C | 96 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(93): Show | 136 | HG00099.hp1 HG00280.hp2 HG00597.hp1 others(133): Show |
intron_variant | MODIFIER | c.266-1627T>G | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43833710 | |||||||
| chr2:43833744 | G | A | 4 | a0001c0001t0003g0011a0002c0002t0002g0010a0002c0002t0002g0048others(1): Show | 6 | HG02896.hp2 HG02897.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.266-1661C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43833744 | |||||||
| chr2:43833770 | T | C | 134 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(131): Show | 181 | HG00099.hp1 HG00280.hp2 HG00597.hp1 others(178): Show |
intron_variant | MODIFIER | c.266-1687A>G | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43833770 | |||||||
| chr2:43833935 | C | T | 1 | a0002c0009t0002g0042 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.266-1852G>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43833935 | |||||||
| chr2:43833982 | C | A | 2 | a0001c0001t0001g0219a0001c0001t0001g0220 | 2 | HG00673.hp1 HG02015.hp1 |
intron_variant | MODIFIER | c.266-1899G>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43833982 | |||||||
| chr2:43834114 | G | C | 5 | a0001c0001t0004g0161a0005c0006t0006g0025a0005c0006t0006g0157others(2): Show | 6 | HG01243.hp1 HG02145.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.266-2031C>G | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43834114 | |||||||
| chr2:43834178 | G | A | 2 | a0001c0001t0001g0221a0002c0002t0002g0222 | 2 | HG02738.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.266-2095C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43834178 | |||||||
| chr2:43834214 | T | A | 1 | a0002c0002t0002g0128 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.266-2131A>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43834214 | |||||||
| chr2:43834243 | T | C | 1 | a0004c0004t0002g0254 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.266-2160A>G | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43834243 | |||||||
| chr2:43834296 | C | T | 3 | a0001c0001t0001g0230a0001c0001t0003g0231a0002c0002t0002g0005 | 6 | HG02647.hp2 HG02809.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.266-2213G>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43834296 | |||||||
| chr2:43834326 | A | G | 1 | a0002c0009t0002g0042 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.266-2243T>C | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43834326 | |||||||
| chr2:43834370 | G | A | 1 | a0002c0009t0002g0042 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.266-2287C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43834370 | |||||||
| chr2:43834466 | T | C | 1 | a0002c0009t0002g0042 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.266-2383A>G | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43834466 | |||||||
| chr2:43834500 | G | A | 2 | a0001c0001t0001g0122a0001c0001t0003g0123 | 2 | HG00280.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.266-2417C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43834500 | |||||||
| chr2:43834570 | T | G | 1 | a0002c0002t0002g0138 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.266-2487A>C | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43834570 | |||||||
| chr2:43834855 | C | T | 1 | a0001c0001t0001g0058 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.266-2772G>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43834855 | |||||||
| chr2:43834892 | C | T | 1 | a0002c0002t0002g0143 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.266-2809G>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43834892 | |||||||
| chr2:43835062 | C | T | 3 | a0005c0006t0006g0025a0005c0006t0006g0157a0005c0006t0006g0158 | 4 | HG01243.hp1 HG02145.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.265+2772G>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43835062 | |||||||
| chr2:43835147 | C | T | 134 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(131): Show | 180 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(177): Show |
intron_variant | MODIFIER | c.265+2687G>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43835147 | |||||||
| chr2:43835237 | ACATTGGC others(20): Show |
A | 139 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(136): Show | 186 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(183): Show |
intron_variant | MODIFIER | c.265+2570_265+2596d others(29): Show |
ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43835237 | |||||||
| chr2:43835293 | TG | T | 17 | a0001c0001t0001g0152a0001c0001t0003g0126a0001c0001t0003g0145others(14): Show | 17 | HG01346.hp2 HG02109.hp2 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.265+2540delC | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43835293 | |||||||
| chr2:43835298 | G | A | 4 | a0002c0002t0002g0026a0002c0002t0002g0164a0002c0002t0002g0165others(1): Show | 5 | HG00642.hp2 HG01099.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.265+2536C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43835298 | |||||||
| chr2:43835375 | A | G | 1 | a0001c0001t0004g0170 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.265+2459T>C | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43835375 | |||||||
| chr2:43835443 | C | T | 1 | a0001c0001t0001g0057 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.265+2391G>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43835443 | |||||||
| chr2:43835645 | G | A | 3 | a0002c0002t0002g0036a0002c0002t0002g0223a0002c0002t0002g0224 | 4 | HG00733.hp2 HG01934.hp1 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.265+2189C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43835645 | |||||||
| chr2:43835732 | C | T | 1 | a0001c0001t0004g0170 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.265+2102G>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43835732 | |||||||
| chr2:43835745 | A | G | 1 | a0001c0001t0001g0169 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.265+2089T>C | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43835745 | |||||||
| chr2:43835757 | G | T | 120 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(117): Show | 161 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(158): Show |
intron_variant | MODIFIER | c.265+2077C>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43835757 | |||||||
| chr2:43835768 | G | T | 1 | a0001c0001t0001g0056 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.265+2066C>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43835768 | |||||||
| chr2:43835811 | T | C | 1 | a0001c0001t0007g0225 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.265+2023A>G | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43835811 | |||||||
| chr2:43835912 | G | A | 1 | a0002c0002t0002g0124 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.265+1922C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43835912 | |||||||
| chr2:43835944 | CT | C | 18 | a0001c0001t0001g0008a0001c0001t0001g0134a0001c0001t0001g0135others(15): Show | 23 | HG01192.hp1 HG01243.hp1 HG01516.hp1 others(20): Show |
intron_variant | MODIFIER | c.265+1889delA | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43835944 | |||||||
| chr2:43835959 | G | C | 18 | a0003c0003t0001g0239a0003c0003t0001g0240a0003c0003t0001g0242others(15): Show | 19 | HG00438.hp1 HG00741.hp2 HG01943.hp2 others(16): Show |
intron_variant | MODIFIER | c.265+1875C>G | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43835959 | |||||||
| chr2:43835960 | A | T | 1 | a0002c0009t0002g0042 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.265+1874T>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43835960 | |||||||
| chr2:43836043 | T | G | 137 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(134): Show | 183 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(180): Show |
intron_variant | MODIFIER | c.265+1791A>C | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43836043 | |||||||
| chr2:43836061 | C | T | 134 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(131): Show | 180 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(177): Show |
intron_variant | MODIFIER | c.265+1773G>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43836061 | |||||||
| chr2:43836176 | A | G | 137 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(134): Show | 183 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(180): Show |
intron_variant | MODIFIER | c.265+1658T>C | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43836176 | |||||||
| chr2:43836188 | G | A | 3 | a0001c0001t0003g0226a0001c0001t0007g0227a0001c0001t0010g0037 | 4 | HG01109.hp1 HG02723.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.265+1646C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43836188 | |||||||
| chr2:43836207 | C | T | 6 | a0001c0001t0001g0012a0001c0001t0001g0051a0001c0001t0001g0052others(3): Show | 7 | HG00741.hp1 HG01070.hp2 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.265+1627G>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43836207 | |||||||
| chr2:43836214 | T | C | 139 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(136): Show | 186 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(183): Show |
intron_variant | MODIFIER | c.265+1620A>G | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43836214 | |||||||
| chr2:43836218 | A | G | 164 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(161): Show | 214 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(211): Show |
intron_variant | MODIFIER | c.265+1616T>C | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43836218 | |||||||
| chr2:43836221 | A | G | 2 | a0006c0005t0002g0009a0006c0005t0008g0043 | 3 | HG01884.hp2 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.265+1613T>C | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43836221 | |||||||
| chr2:43836231 | G | A | 1 | a0001c0001t0001g0228 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.265+1603C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43836231 | |||||||
| chr2:43836246 | A | AT | 2 | a0001c0001t0003g0231a0002c0002t0002g0005 | 5 | HG02647.hp2 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.265+1587dupA | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43836246 | |||||||
| chr2:43836278 | G | T | 4 | a0002c0002t0002g0026a0002c0002t0002g0164a0002c0002t0002g0165others(1): Show | 5 | HG00642.hp2 HG01099.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.265+1556C>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43836278 | |||||||
| chr2:43836324 | T | C | 1 | a0002c0002t0002g0125 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.265+1510A>G | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43836324 | |||||||
| chr2:43836440 | G | C | 2 | a0001c0001t0003g0231a0002c0002t0002g0005 | 5 | HG02647.hp2 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.265+1394C>G | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43836440 | |||||||
| chr2:43836496 | T | C | 6 | a0001c0001t0001g0235a0001c0001t0001g0236a0001c0001t0001g0237others(3): Show | 6 | HG01074.hp1 HG01099.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.265+1338A>G | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43836496 | |||||||
| chr2:43836513 | T | C | 1 | a0001c0001t0003g0229 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.265+1321A>G | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43836513 | |||||||
| chr2:43836548 | A | T | 137 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(134): Show | 183 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(180): Show |
intron_variant | MODIFIER | c.265+1286T>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43836548 | |||||||
| chr2:43836592 | C | T | 13 | a0001c0001t0001g0008a0001c0001t0001g0134a0001c0001t0001g0135others(10): Show | 15 | HG01192.hp1 HG01243.hp1 HG01516.hp1 others(12): Show |
intron_variant | MODIFIER | c.265+1242G>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43836592 | |||||||
| chr2:43836712 | C | T | 2 | a0006c0005t0002g0009a0006c0005t0008g0043 | 3 | HG01884.hp2 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.265+1122G>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43836712 | |||||||
| chr2:43836823 | A | T | 3 | a0001c0001t0001g0004a0001c0001t0001g0167a0001c0001t0001g0168 | 6 | HG00609.hp2 NA18962.hp2 NA18977.hp1 others(3): Show |
intron_variant | MODIFIER | c.265+1011T>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43836823 | |||||||
| chr2:43836923 | C | T | 134 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(131): Show | 180 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(177): Show |
intron_variant | MODIFIER | c.265+911G>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43836923 | |||||||
| chr2:43836958 | G | A | 137 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(134): Show | 183 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(180): Show |
intron_variant | MODIFIER | c.265+876C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43836958 | |||||||
| chr2:43837033 | A | ACG | 97 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(94): Show | 137 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(134): Show |
intron_variant | MODIFIER | c.265+800_265+801ins others(2): Show |
ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43837033 | |||||||
| chr2:43837034 | A | C | 19 | a0001c0001t0001g0139a0001c0001t0001g0152a0001c0001t0003g0145others(16): Show | 20 | HG00642.hp2 HG01099.hp1 HG01346.hp2 others(17): Show |
intron_variant | MODIFIER | c.265+800T>G | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43837034 | |||||||
| chr2:43837035 | G | A | 97 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(94): Show | 137 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(134): Show |
intron_variant | MODIFIER | c.265+799C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43837035 | |||||||
| chr2:43837035 | G | GA | 5 | a0001c0001t0001g0139a0002c0002t0002g0026a0002c0002t0002g0164others(2): Show | 6 | HG00642.hp2 HG01099.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.265+798dupT | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43837035 | |||||||
| chr2:43837119 | T | G | 1 | a0001c0001t0003g0231 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.265+715A>C | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43837119 | |||||||
| chr2:43837120 | CT | C | 123 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(120): Show | 168 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(165): Show |
intron_variant | MODIFIER | c.265+713delA | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43837120 | |||||||
| chr2:43837212 | T | C | 127 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(124): Show | 169 | HG00099.hp1 HG00438.hp2 HG00597.hp1 others(166): Show |
intron_variant | MODIFIER | c.265+622A>G | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43837212 | |||||||
| chr2:43837309 | T | C | 3 | a0001c0001t0001g0230a0001c0001t0003g0231a0002c0002t0002g0005 | 6 | HG02647.hp2 HG02809.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.265+525A>G | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43837309 | |||||||
| chr2:43837645 | G | A | 6 | a0001c0001t0001g0235a0001c0001t0001g0236a0001c0001t0001g0237others(3): Show | 6 | HG01074.hp1 HG01099.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.265+189C>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 2/12 | chr2 | 43837645 | |||||||
| chr2:43838000 | G | T | 2 | a0001c0001t0001g0045a0002c0002t0002g0046 | 2 | HG01346.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.144-45C>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 1/12 | chr2 | 43838000 | |||||||
| chr2:43838060 | C | T | 1 | a0001c0001t0001g0044 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.144-105G>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 1/12 | chr2 | 43838060 | |||||||
| chr2:43838193 | C | A | 1 | a0001c0001t0004g0255 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.144-238G>T | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 1/12 | chr2 | 43838193 | |||||||
| chr2:43838291 | G | T | 2 | a0006c0005t0002g0009a0006c0005t0008g0043 | 3 | HG01884.hp2 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.143+246C>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 1/12 | chr2 | 43838291 | |||||||
| chr2:43838399 | C | T | 1 | a0001c0001t0001g0008 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.143+138G>A | ABCG5 | ENSG00000138075.14 | transcript | ENST00000405322.8 | protein_coding | 1/12 | chr2 | 43838399 |