Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 8534 |
| ensemblid | ENSG00000175264.8 |
| hgncid | 1969 |
| symbol | CHST1 |
| name | carbohydrate sulfotransferase 1 |
| refseq_nuc | NM_003654.6 |
| refseq_prot | NP_003645.1 |
| ensembl_nuc | ENST00000308064.7 |
| ensembl_prot | ENSP00000309270.2 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 45647689 |
| end | 45665622 |
| strand | - |
| ver | v1.2 |
| region | chr11:45647689-45665622 |
| region5000 | chr11:45642689-45670622 |
| regionname0 | CHST1_chr11_45647689_45665622 |
| regionname5000 | CHST1_chr11_45642689_45670622 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 411 | 384 | 94 | 63 | 171 | 16 | 38 | 133 | CHST1_chr11_45642689_45670622 | CHST1 | MQCSW others(406): Show |
chr11 | 45642689 | 45670622 |
| a0002 | 0/0 | 411 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | MQCSW others(406): Show |
chr11 | 45642689 | 45670622 |
| a0003 | 0/0 | 411 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CHST1_chr11_45642689_45670622 | CHST1 | MQCSW others(406): Show |
chr11 | 45642689 | 45670622 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1233 | 230 | 40 | 41 | 103 | 14 | 31 | CHST1_chr11_45642689_45670622 | CHST1 | ATGCA others(1228): Show |
chr11 | 45642689 | 45670622 | ||
| a0001c0002 | 1/0 | 1233 | 152 | 54 | 22 | 66 | 2 | 7 | CHST1_chr11_45642689_45670622 | CHST1 | ATGCA others(1228): Show |
chr11 | 45642689 | 45670622 | ||
| a0001c0005 | 0/0 | 1233 | 1 | 0 | 0 | 1 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | ATGCA others(1228): Show |
chr11 | 45642689 | 45670622 | ||
| a0001c0006 | 0/0 | 1233 | 1 | 0 | 0 | 1 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | ATGCA others(1228): Show |
chr11 | 45642689 | 45670622 | ||
| a0002c0003 | 0/0 | 1233 | 1 | 0 | 1 | 0 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | ATGCA others(1228): Show |
chr11 | 45642689 | 45670622 | ||
| a0003c0004 | 0/0 | 1233 | 1 | 0 | 0 | 1 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | ATGCA others(1228): Show |
chr11 | 45642689 | 45670622 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3905 | 130 | 20 | 24 | 66 | 8 | 12 | CHST1_chr11_45642689_45670622 | CHST1 | GCTCG others(3900): Show |
chr11 | 45642689 | 45670622 |
| a0001c0001t0002 | 0/1 | 3905 | 76 | 16 | 12 | 29 | 5 | 13 | CHST1_chr11_45642689_45670622 | CHST1 | GCTCG others(3900): Show |
chr11 | 45642689 | 45670622 |
| a0001c0001t0003 | 0/0 | 3905 | 1 | 0 | 0 | 0 | 0 | 1 | CHST1_chr11_45642689_45670622 | CHST1 | GCTCG others(3900): Show |
chr11 | 45642689 | 45670622 |
| a0001c0001t0007 | 0/0 | 3905 | 5 | 0 | 1 | 3 | 0 | 1 | CHST1_chr11_45642689_45670622 | CHST1 | GCTCG others(3900): Show |
chr11 | 45642689 | 45670622 |
| a0001c0001t0009 | 0/0 | 3905 | 4 | 0 | 2 | 1 | 0 | 1 | CHST1_chr11_45642689_45670622 | CHST1 | GCTCG others(3900): Show |
chr11 | 45642689 | 45670622 |
| a0001c0001t0010 | 0/0 | 3906 | 1 | 0 | 0 | 0 | 0 | 1 | CHST1_chr11_45642689_45670622 | CHST1 | GCTCG others(3901): Show |
chr11 | 45642689 | 45670622 |
| a0001c0001t0011 | 0/0 | 3905 | 3 | 3 | 0 | 0 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | GCTCG others(3900): Show |
chr11 | 45642689 | 45670622 |
| a0001c0001t0014 | 0/0 | 3905 | 3 | 0 | 0 | 3 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | GCTCG others(3900): Show |
chr11 | 45642689 | 45670622 |
| a0001c0001t0019 | 0/0 | 3905 | 2 | 0 | 1 | 0 | 1 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | GCTCG others(3900): Show |
chr11 | 45642689 | 45670622 |
| a0001c0001t0028 | 0/0 | 3905 | 1 | 0 | 0 | 0 | 0 | 1 | CHST1_chr11_45642689_45670622 | CHST1 | GCTCG others(3900): Show |
chr11 | 45642689 | 45670622 |
| a0001c0001t0029 | 0/0 | 3906 | 1 | 0 | 1 | 0 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | GCTCG others(3901): Show |
chr11 | 45642689 | 45670622 |
| a0001c0001t0036 | 0/0 | 3905 | 1 | 1 | 0 | 0 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | GCTCG others(3900): Show |
chr11 | 45642689 | 45670622 |
| a0001c0001t0040 | 0/0 | 3905 | 1 | 0 | 0 | 0 | 0 | 1 | CHST1_chr11_45642689_45670622 | CHST1 | GCTCG others(3900): Show |
chr11 | 45642689 | 45670622 |
| a0001c0001t0041 | 0/0 | 3906 | 1 | 0 | 0 | 1 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | GCTCG others(3901): Show |
chr11 | 45642689 | 45670622 |
| a0001c0002t0001 | 0/0 | 3905 | 1 | 0 | 1 | 0 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | GCTCG others(3900): Show |
chr11 | 45642689 | 45670622 |
| a0001c0002t0003 | 0/0 | 3905 | 73 | 0 | 12 | 57 | 0 | 4 | CHST1_chr11_45642689_45670622 | CHST1 | GCTCG others(3900): Show |
chr11 | 45642689 | 45670622 |
| a0001c0002t0004 | 0/0 | 3905 | 13 | 13 | 0 | 0 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | GCTCG others(3900): Show |
chr11 | 45642689 | 45670622 |
| a0001c0002t0005 | 0/0 | 3906 | 13 | 12 | 1 | 0 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | GCTCG others(3901): Show |
chr11 | 45642689 | 45670622 |
| a0001c0002t0006 | 0/0 | 3907 | 10 | 9 | 1 | 0 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | GCTCG others(3902): Show |
chr11 | 45642689 | 45670622 |
| a0001c0002t0007 | 0/0 | 3905 | 1 | 0 | 0 | 0 | 0 | 1 | CHST1_chr11_45642689_45670622 | CHST1 | GCTCG others(3900): Show |
chr11 | 45642689 | 45670622 |
| a0001c0002t0008 | 0/0 | 3906 | 5 | 0 | 2 | 0 | 2 | 1 | CHST1_chr11_45642689_45670622 | CHST1 | GCTCG others(3901): Show |
chr11 | 45642689 | 45670622 |
| a0001c0002t0010 | 0/0 | 3906 | 3 | 3 | 0 | 0 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | GCTCG others(3901): Show |
chr11 | 45642689 | 45670622 |
| a0001c0002t0012 | 0/0 | 3905 | 3 | 3 | 0 | 0 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | GCTCG others(3900): Show |
chr11 | 45642689 | 45670622 |
| a0001c0002t0013 | 0/0 | 3905 | 3 | 0 | 0 | 3 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | GCTCG others(3900): Show |
chr11 | 45642689 | 45670622 |
| a0001c0002t0015 | 0/0 | 3906 | 2 | 2 | 0 | 0 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | GCTCG others(3901): Show |
chr11 | 45642689 | 45670622 |
| a0001c0002t0016 | 0/0 | 3906 | 2 | 1 | 1 | 0 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | GCTCG others(3901): Show |
chr11 | 45642689 | 45670622 |
| a0001c0002t0017 | 0/0 | 3905 | 2 | 0 | 2 | 0 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | GCTCG others(3900): Show |
chr11 | 45642689 | 45670622 |
| a0001c0002t0018 | 0/0 | 3905 | 2 | 2 | 0 | 0 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | GCTCG others(3900): Show |
chr11 | 45642689 | 45670622 |
| a0001c0002t0020 | 0/0 | 3905 | 1 | 0 | 0 | 1 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | GCTCG others(3900): Show |
chr11 | 45642689 | 45670622 |
| a0001c0002t0021 | 0/0 | 3906 | 1 | 0 | 1 | 0 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | GCTCG others(3901): Show |
chr11 | 45642689 | 45670622 |
| a0001c0002t0022 | 0/0 | 3907 | 1 | 0 | 0 | 1 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | GCTCG others(3902): Show |
chr11 | 45642689 | 45670622 |
| a0001c0002t0023 | 1/0 | 3906 | 1 | 0 | 0 | 0 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | GCTCG others(3901): Show |
chr11 | 45642689 | 45670622 |
| a0001c0002t0024 | 0/0 | 3906 | 1 | 1 | 0 | 0 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | GCTCG others(3901): Show |
chr11 | 45642689 | 45670622 |
| a0001c0002t0025 | 0/0 | 3905 | 1 | 1 | 0 | 0 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | GCTCG others(3900): Show |
chr11 | 45642689 | 45670622 |
| a0001c0002t0026 | 0/0 | 3905 | 1 | 1 | 0 | 0 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | GCTCG others(3900): Show |
chr11 | 45642689 | 45670622 |
| a0001c0002t0027 | 0/0 | 3905 | 1 | 1 | 0 | 0 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | GCTCG others(3900): Show |
chr11 | 45642689 | 45670622 |
| a0001c0002t0030 | 0/0 | 3907 | 1 | 1 | 0 | 0 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | GCTCG others(3902): Show |
chr11 | 45642689 | 45670622 |
| a0001c0002t0031 | 0/0 | 3906 | 1 | 1 | 0 | 0 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | GCTCG others(3901): Show |
chr11 | 45642689 | 45670622 |
| a0001c0002t0032 | 0/0 | 3907 | 1 | 0 | 1 | 0 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | GCTCG others(3902): Show |
chr11 | 45642689 | 45670622 |
| a0001c0002t0033 | 0/0 | 3905 | 1 | 1 | 0 | 0 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | GCTCG others(3900): Show |
chr11 | 45642689 | 45670622 |
| a0001c0002t0034 | 0/0 | 3905 | 1 | 1 | 0 | 0 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | GCTCG others(3900): Show |
chr11 | 45642689 | 45670622 |
| a0001c0002t0035 | 0/0 | 3906 | 1 | 1 | 0 | 0 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | GCTCG others(3901): Show |
chr11 | 45642689 | 45670622 |
| a0001c0002t0037 | 0/0 | 3905 | 1 | 0 | 0 | 1 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | GCTCG others(3900): Show |
chr11 | 45642689 | 45670622 |
| a0001c0002t0038 | 0/0 | 3905 | 1 | 0 | 0 | 1 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | GCTCG others(3900): Show |
chr11 | 45642689 | 45670622 |
| a0001c0002t0039 | 0/0 | 3906 | 1 | 0 | 0 | 0 | 0 | 1 | CHST1_chr11_45642689_45670622 | CHST1 | GCTCG others(3901): Show |
chr11 | 45642689 | 45670622 |
| a0001c0002t0042 | 0/0 | 3905 | 1 | 0 | 0 | 1 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | GCTCG others(3900): Show |
chr11 | 45642689 | 45670622 |
| a0001c0002t0043 | 0/0 | 3905 | 1 | 0 | 0 | 1 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | GCTCG others(3900): Show |
chr11 | 45642689 | 45670622 |
| a0001c0005t0020 | 0/0 | 3905 | 1 | 0 | 0 | 1 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | GCTCG others(3900): Show |
chr11 | 45642689 | 45670622 |
| a0001c0006t0003 | 0/0 | 3905 | 1 | 0 | 0 | 1 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | GCTCG others(3900): Show |
chr11 | 45642689 | 45670622 |
| a0002c0003t0001 | 0/0 | 3905 | 1 | 0 | 1 | 0 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | GCTCG others(3900): Show |
chr11 | 45642689 | 45670622 |
| a0003c0004t0001 | 0/0 | 3905 | 1 | 0 | 0 | 1 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | GCTCG others(3900): Show |
chr11 | 45642689 | 45670622 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 87 | 9 | 18 | 48 | 6 | 6 | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| a0001c0001t0001g0014 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| a0001c0001t0001g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| a0001c0001t0001g0017 | 0/0 | 3 | 1 | 1 | 0 | 0 | 1 | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| a0001c0001t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| a0001c0001t0002g0002 | 0/0 | 54 | 7 | 11 | 22 | 3 | 11 | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| a0001c0001t0002g0009 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| a0001c0001t0002g0010 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| a0001c0001t0002g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| a0001c0001t0002g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| a0001c0001t0002g0025 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| a0001c0001t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| a0001c0001t0002g0058 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| a0001c0001t0003g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| a0001c0001t0007g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| a0001c0001t0007g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| a0001c0001t0007g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| a0001c0001t0009g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| a0001c0001t0009g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| a0001c0001t0009g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| a0001c0001t0009g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| a0001c0001t0010g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| a0001c0001t0011g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| a0001c0001t0011g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| a0001c0001t0011g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| a0001c0001t0014g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| a0001c0001t0014g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| a0001c0001t0014g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| a0001c0001t0019g0031 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| a0001c0001t0028g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| a0001c0001t0029g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| a0001c0001t0036g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| a0001c0001t0040g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| a0001c0001t0041g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| a0001c0002t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| a0001c0002t0003g0003 | 0/0 | 46 | 0 | 5 | 39 | 0 | 2 | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| a0001c0002t0003g0004 | 0/0 | 9 | 0 | 7 | 2 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| a0001c0002t0003g0006 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| a0001c0002t0003g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| a0001c0002t0003g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| a0001c0002t0003g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| a0001c0002t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| a0001c0002t0003g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| a0001c0002t0003g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| a0001c0002t0003g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| a0001c0002t0003g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| a0001c0002t0004g0007 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| a0001c0002t0004g0013 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| a0001c0002t0004g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| a0001c0002t0004g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| a0001c0002t0005g0005 | 0/0 | 8 | 7 | 1 | 0 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| a0001c0002t0005g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| a0001c0002t0005g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| a0001c0002t0005g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| a0001c0002t0005g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| a0001c0002t0006g0011 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| a0001c0002t0006g0012 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| a0001c0002t0006g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| a0001c0002t0006g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| a0001c0002t0007g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| a0001c0002t0008g0008 | 0/0 | 4 | 0 | 2 | 0 | 1 | 1 | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| a0001c0002t0008g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| a0001c0002t0010g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| a0001c0002t0010g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| a0001c0002t0010g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| a0001c0002t0012g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| a0001c0002t0012g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| a0001c0002t0013g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| a0001c0002t0015g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| a0001c0002t0015g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| a0001c0002t0016g0027 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| a0001c0002t0017g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| a0001c0002t0018g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| a0001c0002t0020g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| a0001c0002t0021g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| a0001c0002t0022g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| a0001c0002t0023g0040 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| a0001c0002t0024g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| a0001c0002t0025g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| a0001c0002t0026g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| a0001c0002t0027g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| a0001c0002t0030g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| a0001c0002t0031g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| a0001c0002t0032g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| a0001c0002t0033g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| a0001c0002t0034g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| a0001c0002t0035g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| a0001c0002t0037g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| a0001c0002t0038g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| a0001c0002t0039g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| a0001c0002t0042g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| a0001c0002t0043g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| a0001c0005t0020g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| a0001c0006t0003g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| a0002c0003t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| a0003c0004t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0113 | EUR | GBR | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG00140 | hp2 | a0001 | c0002 | t0008 | g0008 | EUR | GBR | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG00280 | hp2 | a0001 | c0002 | t0008 | g0042 | EUR | FIN | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0002 | EUR | FIN | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG00323 | hp2 | a0001 | c0001 | t0019 | g0031 | EUR | FIN | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG00408 | hp2 | a0001 | c0002 | t0003 | g0003 | EAS | CHS | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG00423 | hp1 | a0001 | c0001 | t0007 | g0019 | EAS | CHS | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | CHS | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG00438 | hp2 | a0001 | c0002 | t0038 | g0120 | EAS | CHS | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG00544 | hp1 | a0001 | c0002 | t0003 | g0003 | EAS | CHS | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG00558 | hp2 | a0001 | c0002 | t0003 | g0124 | EAS | CHS | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG00597 | hp1 | a0001 | c0001 | t0007 | g0019 | EAS | CHS | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG00621 | hp2 | a0001 | c0002 | t0003 | g0003 | EAS | CHS | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG00639 | hp1 | a0001 | c0001 | t0009 | g0056 | AMR | PUR | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG00639 | hp2 | a0001 | c0002 | t0017 | g0024 | AMR | PUR | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG00733 | hp2 | a0001 | c0002 | t0001 | g0114 | AMR | PUR | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG00738 | hp1 | a0002 | c0003 | t0001 | g0101 | AMR | PUR | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG01071 | hp2 | a0001 | c0002 | t0003 | g0003 | AMR | PUR | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG01099 | hp1 | a0001 | c0002 | t0003 | g0003 | AMR | PUR | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG01099 | hp2 | a0001 | c0002 | t0003 | g0004 | AMR | PUR | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG01106 | hp2 | a0001 | c0002 | t0017 | g0024 | AMR | PUR | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG01109 | hp1 | a0001 | c0002 | t0032 | g0075 | AMR | PUR | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG01109 | hp2 | a0001 | c0002 | t0005 | g0005 | AMR | PUR | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG01167 | hp2 | a0001 | c0002 | t0003 | g0003 | AMR | PUR | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG01168 | hp1 | a0001 | c0002 | t0008 | g0008 | AMR | PUR | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG01169 | hp2 | a0001 | c0002 | t0003 | g0003 | AMR | PUR | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG01175 | hp1 | a0001 | c0001 | t0029 | g0054 | AMR | PUR | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG01243 | hp2 | a0001 | c0002 | t0006 | g0011 | AMR | PUR | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG01257 | hp2 | a0001 | c0002 | t0021 | g0036 | AMR | CLM | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG01258 | hp2 | a0001 | c0002 | t0008 | g0008 | AMR | CLM | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG01361 | hp2 | a0001 | c0002 | t0003 | g0004 | AMR | CLM | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0092 | AMR | CLM | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG01496 | hp1 | a0001 | c0002 | t0016 | g0027 | AMR | CLM | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0025 | EUR | IBS | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0091 | EUR | IBS | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0025 | EUR | IBS | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG01884 | hp1 | a0001 | c0002 | t0004 | g0015 | AFR | ACB | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG01884 | hp2 | a0001 | c0002 | t0005 | g0005 | AFR | ACB | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG01928 | hp1 | a0001 | c0002 | t0003 | g0004 | AMR | PEL | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG01934 | hp1 | a0001 | c0002 | t0003 | g0003 | AMR | PEL | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG01975 | hp1 | a0001 | c0002 | t0003 | g0004 | AMR | PEL | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG01981 | hp1 | a0001 | c0002 | t0003 | g0004 | AMR | PEL | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG01981 | hp2 | a0001 | c0001 | t0007 | g0097 | AMR | PEL | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG01993 | hp1 | a0001 | c0002 | t0003 | g0004 | AMR | PEL | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0057 | AMR | PEL | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | KHV | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG02040 | hp1 | a0001 | c0002 | t0003 | g0003 | EAS | KHV | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG02055 | hp1 | a0001 | c0002 | t0005 | g0005 | AFR | ACB | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG02056 | hp1 | a0001 | c0002 | t0022 | g0041 | EAS | KHV | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG02056 | hp2 | a0001 | c0002 | t0003 | g0003 | EAS | KHV | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | KHV | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG02074 | hp1 | a0001 | c0002 | t0003 | g0035 | EAS | KHV | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG02083 | hp2 | a0001 | c0002 | t0003 | g0123 | EAS | KHV | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | KHV | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG02129 | hp2 | a0001 | c0002 | t0003 | g0021 | EAS | KHV | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG02145 | hp1 | a0001 | c0002 | t0004 | g0013 | AFR | ACB | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0009 | AFR | ACB | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG02165 | hp1 | a0001 | c0002 | t0042 | g0121 | EAS | CDX | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG02165 | hp2 | a0001 | c0002 | t0003 | g0003 | EAS | CDX | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG02257 | hp1 | a0001 | c0002 | t0004 | g0007 | AFR | ACB | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG02258 | hp1 | a0001 | c0002 | t0015 | g0045 | AFR | ACB | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG02258 | hp2 | a0001 | c0002 | t0010 | g0074 | AFR | ACB | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | ACB | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG02280 | hp2 | a0001 | c0001 | t0011 | g0039 | AFR | ACB | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG02293 | hp1 | a0001 | c0001 | t0009 | g0050 | AMR | PEL | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG02293 | hp2 | a0001 | c0001 | t0019 | g0031 | AMR | PEL | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG02300 | hp2 | a0001 | c0002 | t0003 | g0004 | AMR | PEL | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG02451 | hp1 | a0001 | c0002 | t0006 | g0012 | AFR | ACB | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG02523 | hp2 | a0001 | c0002 | t0003 | g0003 | EAS | KHV | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0046 | AFR | GWD | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG02572 | hp2 | a0001 | c0002 | t0030 | g0077 | AFR | GWD | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG02602 | hp1 | a0001 | c0002 | t0003 | g0003 | SAS | PJL | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG02615 | hp1 | a0001 | c0002 | t0005 | g0066 | AFR | GWD | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | GWD | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG02622 | hp1 | a0001 | c0002 | t0006 | g0012 | AFR | GWD | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0009 | AFR | GWD | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG02630 | hp2 | a0001 | c0002 | t0006 | g0011 | AFR | GWD | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG02647 | hp1 | a0001 | c0002 | t0035 | g0079 | AFR | GWD | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG02683 | hp1 | a0001 | c0001 | t0028 | g0053 | SAS | PJL | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG02683 | hp2 | a0001 | c0002 | t0008 | g0008 | SAS | PJL | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG02717 | hp1 | a0001 | c0002 | t0033 | g0076 | AFR | GWD | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG02723 | hp1 | a0001 | c0002 | t0004 | g0007 | AFR | GWD | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG02738 | hp2 | a0001 | c0002 | t0003 | g0003 | SAS | PJL | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG02809 | hp1 | a0001 | c0002 | t0006 | g0071 | AFR | GWD | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0009 | AFR | GWD | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG02818 | hp1 | a0001 | c0002 | t0025 | g0063 | AFR | GWD | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | GWD | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG02886 | hp1 | a0001 | c0002 | t0004 | g0013 | AFR | GWD | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG02886 | hp2 | a0001 | c0002 | t0016 | g0027 | AFR | GWD | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG02895 | hp1 | a0001 | c0001 | t0011 | g0037 | AFR | GWD | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG02896 | hp1 | a0001 | c0001 | t0011 | g0038 | AFR | GWD | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG02896 | hp2 | a0001 | c0002 | t0005 | g0069 | AFR | GWD | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG02922 | hp1 | a0001 | c0002 | t0006 | g0011 | AFR | ESN | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0010 | AFR | ESN | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG02965 | hp1 | a0001 | c0002 | t0005 | g0005 | AFR | ESN | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG02965 | hp2 | a0001 | c0002 | t0027 | g0061 | AFR | ESN | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG02970 | hp1 | a0001 | c0002 | t0010 | g0059 | AFR | ESN | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG02970 | hp2 | a0001 | c0002 | t0015 | g0044 | AFR | ESN | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG02976 | hp1 | a0001 | c0002 | t0010 | g0060 | AFR | ESN | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG02976 | hp2 | a0001 | c0002 | t0005 | g0029 | AFR | ESN | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG03017 | hp2 | a0001 | c0002 | t0003 | g0117 | SAS | PJL | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0009 | AFR | GWD | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG03041 | hp2 | a0001 | c0002 | t0005 | g0029 | AFR | GWD | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | MSL | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG03098 | hp2 | a0001 | c0002 | t0005 | g0005 | AFR | MSL | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG03130 | hp1 | a0001 | c0002 | t0018 | g0028 | AFR | ESN | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG03130 | hp2 | a0001 | c0002 | t0031 | g0078 | AFR | ESN | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0010 | AFR | ESN | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | MSL | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG03209 | hp2 | a0001 | c0002 | t0004 | g0015 | AFR | MSL | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG03225 | hp2 | a0001 | c0002 | t0005 | g0005 | AFR | MSL | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0099 | SAS | PJL | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0125 | SAS | PJL | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | MSL | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG03453 | hp2 | a0001 | c0002 | t0012 | g0026 | AFR | MSL | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG03486 | hp1 | a0001 | c0002 | t0004 | g0007 | AFR | MSL | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | MSL | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG03492 | hp2 | a0001 | c0001 | t0007 | g0104 | SAS | PJL | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG03516 | hp1 | a0001 | c0002 | t0006 | g0070 | AFR | ESN | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG03516 | hp2 | a0001 | c0002 | t0018 | g0028 | AFR | ESN | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG03540 | hp1 | a0001 | c0002 | t0006 | g0012 | AFR | GWD | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG03540 | hp2 | a0001 | c0002 | t0004 | g0013 | AFR | GWD | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG03579 | hp1 | a0001 | c0002 | t0034 | g0064 | AFR | MSL | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG03579 | hp2 | a0001 | c0002 | t0004 | g0007 | AFR | MSL | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG03654 | hp1 | a0001 | c0001 | t0040 | g0100 | SAS | PJL | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0088 | SAS | STU | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0047 | SAS | PJL | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG03831 | hp1 | a0001 | c0002 | t0003 | g0105 | SAS | BEB | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0073 | SAS | BEB | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0084 | SAS | BEB | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG03927 | hp2 | a0001 | c0001 | t0003 | g0096 | SAS | BEB | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | BEB | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG03942 | hp2 | a0001 | c0001 | t0010 | g0072 | SAS | BEB | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0086 | SAS | STU | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | STU | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG04184 | hp1 | a0001 | c0001 | t0009 | g0049 | SAS | BEB | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG04184 | hp2 | a0001 | c0002 | t0039 | g0083 | SAS | BEB | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | STU | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | STU | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | STU | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG04228 | hp2 | a0001 | c0002 | t0007 | g0115 | SAS | STU | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA18522 | hp1 | a0001 | c0002 | t0004 | g0015 | AFR | YRI | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | YRI | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | YRI | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA18906 | hp2 | a0001 | c0002 | t0005 | g0067 | AFR | YRI | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA18941 | hp2 | a0001 | c0002 | t0043 | g0129 | EAS | JPT | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA18943 | hp1 | a0001 | c0002 | t0003 | g0003 | EAS | JPT | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA18943 | hp2 | a0001 | c0002 | t0003 | g0021 | EAS | JPT | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA18945 | hp2 | a0001 | c0002 | t0003 | g0003 | EAS | JPT | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA18946 | hp1 | a0001 | c0002 | t0003 | g0006 | EAS | JPT | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA18948 | hp2 | a0001 | c0002 | t0003 | g0003 | EAS | JPT | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA18949 | hp1 | a0001 | c0002 | t0003 | g0003 | EAS | JPT | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA18950 | hp1 | a0001 | c0002 | t0003 | g0003 | EAS | JPT | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA18954 | hp1 | a0001 | c0002 | t0003 | g0085 | EAS | JPT | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA18956 | hp2 | a0001 | c0002 | t0003 | g0003 | EAS | JPT | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA18963 | hp2 | a0001 | c0002 | t0020 | g0119 | EAS | JPT | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA18964 | hp1 | a0001 | c0002 | t0003 | g0003 | EAS | JPT | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA18965 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA18966 | hp1 | a0001 | c0002 | t0003 | g0003 | EAS | JPT | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA18967 | hp2 | a0001 | c0006 | t0003 | g0122 | EAS | JPT | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA18970 | hp1 | a0001 | c0002 | t0003 | g0003 | EAS | JPT | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA18974 | hp1 | a0001 | c0001 | t0014 | g0109 | EAS | JPT | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA18974 | hp2 | a0001 | c0002 | t0013 | g0020 | EAS | JPT | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA18979 | hp2 | a0001 | c0002 | t0003 | g0032 | EAS | JPT | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA18980 | hp1 | a0001 | c0002 | t0003 | g0003 | EAS | JPT | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA18983 | hp1 | a0001 | c0002 | t0003 | g0003 | EAS | JPT | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA18984 | hp2 | a0001 | c0002 | t0003 | g0003 | EAS | JPT | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA18985 | hp2 | a0001 | c0002 | t0003 | g0003 | EAS | JPT | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA18987 | hp1 | a0001 | c0002 | t0003 | g0003 | EAS | JPT | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA18988 | hp1 | a0001 | c0002 | t0013 | g0020 | EAS | JPT | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA18990 | hp2 | a0001 | c0002 | t0003 | g0003 | EAS | JPT | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA18991 | hp1 | a0001 | c0002 | t0003 | g0035 | EAS | JPT | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA18993 | hp1 | a0001 | c0002 | t0003 | g0006 | EAS | JPT | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA18994 | hp2 | a0001 | c0002 | t0003 | g0004 | EAS | JPT | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA18995 | hp2 | a0001 | c0002 | t0037 | g0081 | EAS | JPT | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA18998 | hp1 | a0001 | c0002 | t0003 | g0003 | EAS | JPT | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA18999 | hp2 | a0001 | c0002 | t0003 | g0003 | EAS | JPT | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA19002 | hp2 | a0001 | c0002 | t0003 | g0003 | EAS | JPT | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA19003 | hp1 | a0003 | c0004 | t0001 | g0102 | EAS | JPT | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA19003 | hp2 | a0001 | c0002 | t0003 | g0003 | EAS | JPT | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA19007 | hp2 | a0001 | c0002 | t0003 | g0006 | EAS | JPT | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA19010 | hp1 | a0001 | c0002 | t0003 | g0003 | EAS | JPT | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA19010 | hp2 | a0001 | c0002 | t0003 | g0003 | EAS | JPT | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA19011 | hp1 | a0001 | c0001 | t0041 | g0103 | EAS | JPT | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA19011 | hp2 | a0001 | c0002 | t0013 | g0020 | EAS | JPT | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | LWK | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0010 | AFR | LWK | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0010 | AFR | LWK | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA19043 | hp2 | a0001 | c0002 | t0012 | g0062 | AFR | LWK | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA19054 | hp1 | a0001 | c0001 | t0014 | g0090 | EAS | JPT | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA19055 | hp1 | a0001 | c0002 | t0003 | g0003 | EAS | JPT | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA19056 | hp2 | a0001 | c0002 | t0003 | g0021 | EAS | JPT | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA19057 | hp1 | a0001 | c0002 | t0003 | g0003 | EAS | JPT | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA19058 | hp1 | a0001 | c0002 | t0003 | g0032 | EAS | JPT | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA19058 | hp2 | a0001 | c0002 | t0003 | g0003 | EAS | JPT | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA19063 | hp2 | a0001 | c0002 | t0003 | g0006 | EAS | JPT | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA19064 | hp1 | a0001 | c0002 | t0003 | g0003 | EAS | JPT | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA19065 | hp2 | a0001 | c0002 | t0003 | g0006 | EAS | JPT | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA19066 | hp2 | a0001 | c0002 | t0003 | g0003 | EAS | JPT | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA19067 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA19068 | hp1 | a0001 | c0001 | t0007 | g0019 | EAS | JPT | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA19070 | hp2 | a0001 | c0002 | t0003 | g0004 | EAS | JPT | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA19077 | hp2 | a0001 | c0002 | t0003 | g0003 | EAS | JPT | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA19079 | hp1 | a0001 | c0002 | t0003 | g0003 | EAS | JPT | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA19080 | hp2 | a0001 | c0002 | t0003 | g0003 | EAS | JPT | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA19082 | hp1 | a0001 | c0002 | t0003 | g0006 | EAS | JPT | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA19084 | hp2 | a0001 | c0002 | t0003 | g0003 | EAS | JPT | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA19085 | hp1 | a0001 | c0002 | t0003 | g0003 | EAS | JPT | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA19087 | hp1 | a0001 | c0002 | t0003 | g0003 | EAS | JPT | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA19087 | hp2 | a0001 | c0001 | t0009 | g0052 | EAS | JPT | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA19088 | hp2 | a0001 | c0005 | t0020 | g0118 | EAS | JPT | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA19089 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA19089 | hp2 | a0001 | c0001 | t0014 | g0098 | EAS | JPT | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA19240 | hp1 | a0001 | c0002 | t0005 | g0005 | AFR | YRI | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | YRI | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA20129 | hp1 | a0001 | c0002 | t0004 | g0065 | AFR | ASW | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ASW | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0002 | EUR | TSI | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0002 | EUR | TSI | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | ACB | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG02486 | hp1 | a0001 | c0002 | t0012 | g0026 | AFR | ACB | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG02486 | hp2 | a0001 | c0002 | t0006 | g0012 | AFR | ACB | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG02559 | hp2 | a0001 | c0001 | t0036 | g0080 | AFR | ACB | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG03471 | hp1 | a0001 | c0002 | t0004 | g0007 | AFR | MSL | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG03471 | hp2 | a0001 | c0002 | t0026 | g0068 | AFR | MSL | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG06807 | hp1 | a0001 | c0002 | t0024 | g0043 | AFR | USA | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| HG06807 | hp2 | a0001 | c0002 | t0004 | g0013 | AFR | USA | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA20300 | hp1 | a0001 | c0002 | t0006 | g0011 | AFR | USA | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA20300 | hp2 | a0001 | c0002 | t0005 | g0005 | AFR | USA | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | LWK | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0058 | REF | REF | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0023 | g0040 | REF | REF | CHST1_chr11_45642689_45670622 | CHST1 | chr11 | 45642689 | 45670622 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:45649902 | G | A | 1 | a0002 | 1 | HG00738.hp1 | missense_variant | MODERATE | c.1022C>T | p.Thr341Ile | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 4/4 | 1693/3906 | 1022/1236 | 341/411 | chr11 | 45649902 | |||
| chr11:45650711 | A | C | 1 | a0003 | 1 | NA19003.hp1 | missense_variant | MODERATE | c.213T>G | p.Ser71Arg | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 4/4 | 884/3906 | 213/1236 | 71/411 | chr11 | 45650711 | |||
| chr11:45665179 | T | G | 1 | a0001 | 1 | HG01257.hp2 | splice_region_variant | LOW | c.-228A>C | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/4 | chr11 | 45665179 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:45650696 | C | G | 1 | a0001c0005 | 1 | NA19088.hp2 | synonymous_variant | LOW | c.228G>C | p.Val76Val | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 4/4 | 899/3906 | 228/1236 | 76/411 | chr11 | 45650696 | |||
| chr11:45650708 | G | A | 1 | a0001c0006 | 1 | NA18967.hp2 | synonymous_variant | LOW | c.216C>T | p.Gly72Gly | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 4/4 | 887/3906 | 216/1236 | 72/411 | chr11 | 45650708 | |||
| chr11:45650711 | A | G | 2 | a0001c0001 a0002c0003 |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
synonymous_variant | LOW | c.213T>C | p.Ser71Ser | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 4/4 | 884/3906 | 213/1236 | 71/411 | chr11 | 45650711 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:45647856 | G | A | 1 | a0001c0002t0038 | 1 | HG00438.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1832C>T | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 4/4 | 1832 | chr11 | 45647856 | ||||||
| chr11:45647897 | G | T | 1 | a0001c0001t0028 | 1 | HG02683.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1791C>A | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 4/4 | 1791 | chr11 | 45647897 | ||||||
| chr11:45647950 | T | G | 1 | a0001c0002t0015 | 2 | HG02258.hp1 HG02970.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1738A>C | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 4/4 | 1738 | chr11 | 45647950 | ||||||
| chr11:45648049 | C | T | 3 | a0001c0002t0004 a0001c0002t0031 a0001c0002t0034 |
15 | HG01884.hp1 HG02145.hp1 HG02257.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1639G>A | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 4/4 | 1639 | chr11 | 45648049 | ||||||
| chr11:45648059 | G | T | 3 | a0001c0002t0004 a0001c0002t0031 a0001c0002t0034 |
15 | HG01884.hp1 HG02145.hp1 HG02257.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1629C>A | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 4/4 | 1629 | chr11 | 45648059 | ||||||
| chr11:45648097 | C | T | 1 | a0001c0002t0026 | 1 | HG03471.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1591G>A | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 4/4 | 1591 | chr11 | 45648097 | ||||||
| chr11:45648100 | T | C | 1 | a0001c0002t0030 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1588A>G | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 4/4 | 1588 | chr11 | 45648100 | ||||||
| chr11:45648115 | C | G | 7 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0011 others(4): Show |
87 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(84): Show |
3_prime_UTR_variant | MODIFIER | c.*1573G>C | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 4/4 | 1573 | chr11 | 45648115 | ||||||
| chr11:45648198 | C | T | 4 | a0001c0002t0012 a0001c0002t0016 a0001c0002t0025 others(1): Show |
7 | HG01496.hp1 HG02486.hp1 HG02717.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1490G>A | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 4/4 | 1490 | chr11 | 45648198 | ||||||
| chr11:45648266 | A | T | 2 | a0001c0002t0020 a0001c0005t0020 |
2 | NA18963.hp2 NA19088.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1422T>A | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 4/4 | 1422 | chr11 | 45648266 | ||||||
| chr11:45648399 | C | T | 12 | a0001c0001t0003 a0001c0002t0003 a0001c0002t0013 others(9): Show |
87 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(84): Show |
3_prime_UTR_variant | MODIFIER | c.*1289G>A | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 4/4 | 1289 | chr11 | 45648399 | ||||||
| chr11:45648408 | G | A | 1 | a0001c0002t0013 | 3 | NA18974.hp2 NA18988.hp1 NA19011.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1280C>T | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 4/4 | 1280 | chr11 | 45648408 | ||||||
| chr11:45648525 | T | TA | 10 | a0001c0001t0010 a0001c0001t0029 a0001c0002t0008 others(7): Show |
17 | HG00140.hp2 HG00280.hp2 HG01168.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*1162_*1163insT | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 4/4 | 1162 | chr11 | 45648525 | ||||||
| chr11:45648526 | C | A | 24 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0007 others(21): Show |
200 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(197): Show |
3_prime_UTR_variant | MODIFIER | c.*1162G>T | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 4/4 | 1162 | chr11 | 45648526 | ||||||
| chr11:45648527 | C | A | 10 | a0001c0001t0010 a0001c0001t0029 a0001c0002t0008 others(7): Show |
17 | HG00140.hp2 HG00280.hp2 HG01168.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*1161G>T | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 4/4 | 1161 | chr11 | 45648527 | ||||||
| chr11:45648527 | C | CAA | 4 | a0001c0002t0006 a0001c0002t0022 a0001c0002t0030 others(1): Show |
13 | HG01109.hp1 HG01243.hp2 HG02056.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1159_*1160dupTT | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 4/4 | 1160 | chr11 | 45648527 | ||||||
| chr11:45648543 | T | A | 3 | a0001c0002t0004 a0001c0002t0031 a0001c0002t0034 |
15 | HG01884.hp1 HG02145.hp1 HG02257.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1145A>T | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 4/4 | 1145 | chr11 | 45648543 | ||||||
| chr11:45648666 | G | A | 1 | a0001c0002t0015 | 2 | HG02258.hp1 HG02970.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1022C>T | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 4/4 | 1022 | chr11 | 45648666 | ||||||
| chr11:45648763 | T | C | 1 | a0001c0001t0040 | 1 | HG03654.hp1 | 3_prime_UTR_variant | MODIFIER | c.*925A>G | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 4/4 | 925 | chr11 | 45648763 | ||||||
| chr11:45648772 | T | A | 1 | a0001c0002t0032 | 1 | HG01109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*916A>T | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 4/4 | 916 | chr11 | 45648772 | ||||||
| chr11:45648845 | C | T | 11 | a0001c0001t0003 a0001c0002t0003 a0001c0002t0013 others(8): Show |
86 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(83): Show |
3_prime_UTR_variant | MODIFIER | c.*843G>A | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 4/4 | 843 | chr11 | 45648845 | ||||||
| chr11:45649419 | C | T | 1 | a0001c0001t0019 | 2 | HG00323.hp2 HG02293.hp2 |
3_prime_UTR_variant | MODIFIER | c.*269G>A | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 4/4 | 269 | chr11 | 45649419 | ||||||
| chr11:45649450 | TG | T | 47 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(44): Show |
368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
3_prime_UTR_variant | MODIFIER | c.*237delC | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 4/4 | 237 | chr11 | 45649450 | ||||||
| chr11:45649455 | G | T | 1 | a0001c0001t0041 | 1 | NA19011.hp1 | 3_prime_UTR_variant | MODIFIER | c.*233C>A | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 4/4 | 233 | chr11 | 45649455 | ||||||
| chr11:45649456 | G | T | 43 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(40): Show |
361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
3_prime_UTR_variant | MODIFIER | c.*232C>A | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 4/4 | 232 | chr11 | 45649456 | ||||||
| chr11:45649460 | G | T | 1 | a0001c0002t0025 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*228C>A | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 4/4 | 228 | chr11 | 45649460 | ||||||
| chr11:45649471 | C | A | 1 | a0001c0001t0014 | 3 | NA18974.hp1 NA19054.hp1 NA19089.hp2 |
3_prime_UTR_variant | MODIFIER | c.*217G>T | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 4/4 | 217 | chr11 | 45649471 | ||||||
| chr11:45649475 | C | T | 3 | a0001c0002t0012 a0001c0002t0016 a0001c0002t0025 |
6 | HG01496.hp1 HG02486.hp1 HG02818.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*213G>A | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 4/4 | 213 | chr11 | 45649475 | ||||||
| chr11:45649550 | G | C | 1 | a0001c0002t0042 | 1 | HG02165.hp1 | 3_prime_UTR_variant | MODIFIER | c.*138C>G | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 4/4 | 138 | chr11 | 45649550 | ||||||
| chr11:45649685 | G | A | 2 | a0001c0002t0005 a0001c0002t0018 |
15 | HG01109.hp2 HG01884.hp2 HG02055.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*3C>T | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 4/4 | 3 | chr11 | 45649685 | ||||||
| chr11:45649686 | G | A | 1 | a0001c0002t0034 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2C>T | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 4/4 | 2 | chr11 | 45649686 | ||||||
| chr11:45665228 | C | G | 1 | a0001c0002t0021 | 1 | HG01257.hp2 | 5_prime_UTR_variant | MODIFIER | c.-277G>C | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/4 | 14305 | chr11 | 45665228 | ||||||
| chr11:45665239 | G | T | 1 | a0001c0002t0015 | 2 | HG02258.hp1 HG02970.hp2 |
5_prime_UTR_variant | MODIFIER | c.-288C>A | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/4 | 14316 | chr11 | 45665239 | ||||||
| chr11:45665247 | G | C | 1 | a0001c0002t0021 | 1 | HG01257.hp2 | 5_prime_UTR_variant | MODIFIER | c.-296C>G | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/4 | 14324 | chr11 | 45665247 | ||||||
| chr11:45665250 | G | A | 1 | a0001c0002t0035 | 1 | HG02647.hp1 | 5_prime_UTR_variant | MODIFIER | c.-299C>T | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/4 | 14327 | chr11 | 45665250 | ||||||
| chr11:45665251 | C | G | 1 | a0001c0002t0021 | 1 | HG01257.hp2 | 5_prime_UTR_variant | MODIFIER | c.-300G>C | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/4 | 14328 | chr11 | 45665251 | ||||||
| chr11:45665255 | G | T | 1 | a0001c0002t0021 | 1 | HG01257.hp2 | 5_prime_UTR_variant | MODIFIER | c.-304C>A | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/4 | 14332 | chr11 | 45665255 | ||||||
| chr11:45665259 | C | T | 1 | a0001c0002t0037 | 1 | NA18995.hp2 | 5_prime_UTR_variant | MODIFIER | c.-308G>A | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/4 | 14336 | chr11 | 45665259 | ||||||
| chr11:45665262 | C | G | 1 | a0001c0002t0021 | 1 | HG01257.hp2 | 5_prime_UTR_variant | MODIFIER | c.-311G>C | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/4 | 14339 | chr11 | 45665262 | ||||||
| chr11:45665387 | G | A | 1 | a0001c0001t0036 | 1 | HG02559.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-436C>T | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/4 | chr11 | 45665387 | |||||||
| chr11:45665452 | G | T | 1 | a0001c0002t0024 | 1 | HG06807.hp1 | 5_prime_UTR_variant | MODIFIER | c.-501C>A | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/4 | 14529 | chr11 | 45665452 | ||||||
| chr11:45665522 | C | T | 25 | a0001c0001t0002 a0001c0001t0009 a0001c0001t0010 others(22): Show |
143 | HG00323.hp1 HG00408.hp1 HG00597.hp2 others(140): Show |
5_prime_UTR_variant | MODIFIER | c.-571G>A | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/4 | 14599 | chr11 | 45665522 | ||||||
| chr11:45665530 | G | A | 1 | a0001c0002t0043 | 1 | NA18941.hp2 | 5_prime_UTR_variant | MODIFIER | c.-579C>T | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/4 | 14607 | chr11 | 45665530 | ||||||
| chr11:45665616 | T | G | 46 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(43): Show |
374 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(371): Show |
5_prime_UTR_variant | MODIFIER | c.-665A>C | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/4 | 14693 | chr11 | 45665616 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:45651044 | A | G | 121 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0016 others(118): Show |
369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.-42-79T>C | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 3/3 | chr11 | 45651044 | |||||||
| chr11:45651169 | A | G | 3 | a0001c0002t0010g0059 a0001c0002t0010g0060 a0001c0002t0035g0079 |
3 | HG02647.hp1 HG02970.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-42-204T>C | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 3/3 | chr11 | 45651169 | |||||||
| chr11:45651175 | T | C | 74 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0016 others(71): Show |
241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.-42-210A>G | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 3/3 | chr11 | 45651175 | |||||||
| chr11:45651197 | G | A | 67 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0016 others(64): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.-42-232C>T | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 3/3 | chr11 | 45651197 | |||||||
| chr11:45651215 | C | A | 5 | a0001c0002t0006g0012 a0001c0002t0006g0071 a0001c0002t0030g0077 others(2): Show |
8 | HG01109.hp1 HG02451.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.-42-250G>T | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 3/3 | chr11 | 45651215 | |||||||
| chr11:45651351 | G | A | 1 | a0001c0001t0041g0103 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-42-386C>T | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 3/3 | chr11 | 45651351 | |||||||
| chr11:45651376 | G | T | 45 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0016 others(42): Show |
145 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(142): Show |
intron_variant | MODIFIER | c.-42-411C>A | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 3/3 | chr11 | 45651376 | |||||||
| chr11:45651464 | A | C | 22 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0010 others(19): Show |
86 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.-42-499T>G | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 3/3 | chr11 | 45651464 | |||||||
| chr11:45651503 | G | A | 1 | a0001c0001t0001g0091 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-43+490C>T | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 3/3 | chr11 | 45651503 | |||||||
| chr11:45651669 | T | C | 1 | a0001c0001t0002g0047 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-43+324A>G | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 3/3 | chr11 | 45651669 | |||||||
| chr11:45651896 | C | A | 1 | a0001c0001t0001g0018 | 3 | HG01346.hp2 HG01358.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.-43+97G>T | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 3/3 | chr11 | 45651896 | |||||||
| chr11:45651943 | G | A | 3 | a0001c0002t0006g0012 a0001c0002t0030g0077 a0001c0002t0033g0076 |
6 | HG02451.hp1 HG02486.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.-43+50C>T | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 3/3 | chr11 | 45651943 | |||||||
| chr11:45652244 | C | T | 2 | a0001c0002t0005g0067 a0001c0002t0005g0069 |
2 | HG02896.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-140-154G>A | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 2/3 | chr11 | 45652244 | |||||||
| chr11:45652620 | C | T | 67 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0016 others(64): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.-226-14G>A | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45652620 | |||||||
| chr11:45652716 | C | T | 47 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0016 others(44): Show |
147 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(144): Show |
intron_variant | MODIFIER | c.-226-110G>A | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45652716 | |||||||
| chr11:45652837 | C | T | 7 | a0001c0002t0006g0011 a0001c0002t0006g0070 a0001c0002t0010g0059 others(4): Show |
10 | HG01243.hp2 HG02258.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.-226-231G>A | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45652837 | |||||||
| chr11:45652988 | C | G | 1 | a0001c0002t0005g0066 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-226-382G>C | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45652988 | |||||||
| chr11:45653030 | C | T | 2 | a0001c0002t0006g0011 a0001c0002t0006g0070 |
5 | HG01243.hp2 HG02630.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.-226-424G>A | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45653030 | |||||||
| chr11:45653049 | G | T | 69 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0016 others(66): Show |
233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.-226-443C>A | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45653049 | |||||||
| chr11:45653152 | C | T | 1 | a0001c0001t0001g0099 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-226-546G>A | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45653152 | |||||||
| chr11:45653291 | C | T | 2 | a0001c0002t0006g0011 a0001c0002t0006g0070 |
5 | HG01243.hp2 HG02630.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.-226-685G>A | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45653291 | |||||||
| chr11:45653531 | A | ACT | 48 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0016 others(45): Show |
148 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(145): Show |
intron_variant | MODIFIER | c.-226-926_-226-925i others(4): Show |
CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45653531 | |||||||
| chr11:45653538 | C | G | 2 | a0001c0002t0015g0044 a0001c0002t0015g0045 |
2 | HG02258.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.-226-932G>C | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45653538 | |||||||
| chr11:45653623 | TG | T | 5 | a0001c0002t0008g0008 a0001c0002t0008g0042 a0001c0002t0021g0036 others(2): Show |
8 | HG00140.hp2 HG00280.hp2 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.-226-1018delC | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45653623 | |||||||
| chr11:45653693 | T | C | 1 | a0001c0001t0002g0010 | 4 | HG02922.hp2 HG03139.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.-226-1087A>G | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45653693 | |||||||
| chr11:45653870 | C | T | 5 | a0001c0002t0004g0007 a0001c0002t0004g0013 a0001c0002t0004g0015 others(2): Show |
14 | HG01884.hp1 HG02145.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.-226-1264G>A | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45653870 | |||||||
| chr11:45654057 | C | G | 2 | a0001c0001t0002g0009 a0001c0001t0002g0046 |
5 | HG02145.hp2 HG02572.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.-226-1451G>C | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45654057 | |||||||
| chr11:45654235 | A | G | 1 | a0001c0002t0003g0117 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-226-1629T>C | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45654235 | |||||||
| chr11:45654326 | A | G | 4 | a0001c0002t0008g0008 a0001c0002t0008g0042 a0001c0002t0021g0036 others(1): Show |
7 | HG00140.hp2 HG00280.hp2 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.-226-1720T>C | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45654326 | |||||||
| chr11:45654331 | G | A | 2 | a0001c0002t0015g0044 a0001c0002t0015g0045 |
2 | HG02258.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.-226-1725C>T | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45654331 | |||||||
| chr11:45654397 | C | G | 1 | a0001c0001t0002g0051 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.-226-1791G>C | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45654397 | |||||||
| chr11:45654407 | A | G | 1 | a0001c0002t0027g0061 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-226-1801T>C | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45654407 | |||||||
| chr11:45654426 | G | A | 1 | a0001c0002t0006g0011 | 4 | HG01243.hp2 HG02630.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.-226-1820C>T | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45654426 | |||||||
| chr11:45654551 | C | T | 1 | a0001c0001t0010g0072 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-226-1945G>A | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45654551 | |||||||
| chr11:45654572 | C | A | 1 | a0001c0001t0001g0033 | 2 | NA18994.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.-226-1966G>T | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45654572 | |||||||
| chr11:45654635 | G | A | 1 | a0001c0002t0003g0021 | 3 | HG02129.hp2 NA18943.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.-226-2029C>T | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45654635 | |||||||
| chr11:45654814 | T | C | 48 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0016 others(45): Show |
148 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(145): Show |
intron_variant | MODIFIER | c.-226-2208A>G | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45654814 | |||||||
| chr11:45654937 | G | A | 6 | a0001c0002t0012g0026 a0001c0002t0012g0062 a0001c0002t0016g0027 others(3): Show |
8 | HG01496.hp1 HG02486.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.-226-2331C>T | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45654937 | |||||||
| chr11:45655160 | G | A | 7 | a0001c0002t0012g0026 a0001c0002t0012g0062 a0001c0002t0016g0027 others(4): Show |
9 | HG01496.hp1 HG02486.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.-226-2554C>T | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45655160 | |||||||
| chr11:45655214 | G | A | 1 | a0001c0001t0001g0092 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-226-2608C>T | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45655214 | |||||||
| chr11:45655234 | C | T | 22 | a0001c0001t0007g0019 a0001c0002t0001g0114 a0001c0002t0003g0003 others(19): Show |
88 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.-226-2628G>A | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45655234 | |||||||
| chr11:45655273 | C | T | 45 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0016 others(42): Show |
145 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(142): Show |
intron_variant | MODIFIER | c.-226-2667G>A | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45655273 | |||||||
| chr11:45655479 | T | C | 19 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0010 others(16): Show |
81 | HG00323.hp1 HG00408.hp1 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.-226-2873A>G | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45655479 | |||||||
| chr11:45655681 | C | A | 2 | a0001c0002t0006g0011 a0001c0002t0006g0070 |
5 | HG01243.hp2 HG02630.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.-226-3075G>T | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45655681 | |||||||
| chr11:45655893 | C | T | 1 | a0001c0002t0007g0115 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-226-3287G>A | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45655893 | |||||||
| chr11:45656365 | G | T | 1 | a0001c0002t0037g0081 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.-226-3759C>A | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45656365 | |||||||
| chr11:45656366 | A | T | 1 | a0001c0002t0037g0081 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.-226-3760T>A | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45656366 | |||||||
| chr11:45656668 | T | C | 1 | a0001c0002t0015g0044 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-226-4062A>G | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45656668 | |||||||
| chr11:45656727 | C | G | 3 | a0001c0001t0014g0090 a0001c0001t0014g0098 a0001c0001t0014g0109 |
3 | NA18974.hp1 NA19054.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.-226-4121G>C | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45656727 | |||||||
| chr11:45656728 | C | A | 1 | a0001c0002t0010g0074 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-226-4122G>T | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45656728 | |||||||
| chr11:45656728 | C | T | 4 | a0001c0002t0001g0114 a0001c0002t0003g0004 a0001c0002t0003g0006 others(1): Show |
17 | HG00733.hp2 HG01099.hp2 HG01361.hp2 others(14): Show |
intron_variant | MODIFIER | c.-226-4122G>A | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45656728 | |||||||
| chr11:45656730 | C | G | 1 | a0001c0002t0027g0061 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-226-4124G>C | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45656730 | |||||||
| chr11:45656902 | G | A | 5 | a0001c0002t0004g0007 a0001c0002t0004g0013 a0001c0002t0004g0015 others(2): Show |
14 | HG01884.hp1 HG02145.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.-226-4296C>T | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45656902 | |||||||
| chr11:45656912 | G | C | 1 | a0001c0002t0003g0124 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-226-4306C>G | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45656912 | |||||||
| chr11:45656934 | G | A | 7 | a0001c0002t0012g0026 a0001c0002t0016g0027 a0001c0002t0024g0043 others(4): Show |
9 | HG01496.hp1 HG02486.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.-226-4328C>T | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45656934 | |||||||
| chr11:45657035 | T | C | 3 | a0001c0001t0011g0037 a0001c0001t0011g0038 a0001c0002t0005g0069 |
3 | HG02895.hp1 HG02896.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.-226-4429A>G | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45657035 | |||||||
| chr11:45657075 | ATGGGGTC others(9): Show |
A | 1 | a0001c0002t0027g0061 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-226-4485_-226-447 others(20): Show |
CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45657075 | |||||||
| chr11:45657214 | A | G | 1 | a0001c0002t0004g0007 | 5 | HG02257.hp1 HG02723.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.-226-4608T>C | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45657214 | |||||||
| chr11:45657218 | C | G | 47 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0016 others(44): Show |
150 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(147): Show |
intron_variant | MODIFIER | c.-226-4612G>C | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45657218 | |||||||
| chr11:45657260 | A | C | 4 | a0001c0002t0008g0008 a0001c0002t0008g0042 a0001c0002t0021g0036 others(1): Show |
7 | HG00140.hp2 HG00280.hp2 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.-226-4654T>G | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45657260 | |||||||
| chr11:45657270 | C | T | 60 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0016 others(57): Show |
172 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(169): Show |
intron_variant | MODIFIER | c.-226-4664G>A | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45657270 | |||||||
| chr11:45657306 | GA | G | 60 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0016 others(57): Show |
172 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(169): Show |
intron_variant | MODIFIER | c.-226-4701delT | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45657306 | |||||||
| chr11:45657571 | C | T | 1 | a0001c0002t0027g0061 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-226-4965G>A | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45657571 | |||||||
| chr11:45657647 | A | G | 85 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0016 others(82): Show |
265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.-226-5041T>C | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45657647 | |||||||
| chr11:45657662 | C | T | 15 | a0001c0002t0004g0007 a0001c0002t0004g0013 a0001c0002t0004g0015 others(12): Show |
27 | HG01109.hp1 HG01243.hp2 HG01884.hp1 others(24): Show |
intron_variant | MODIFIER | c.-226-5056G>A | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45657662 | |||||||
| chr11:45657762 | T | C | 1 | a0001c0002t0022g0041 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-226-5156A>G | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45657762 | |||||||
| chr11:45657923 | C | G | 2 | a0001c0001t0003g0096 a0001c0001t0007g0097 |
2 | HG01981.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.-226-5317G>C | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45657923 | |||||||
| chr11:45658115 | A | G | 1 | a0001c0001t0001g0106 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.-226-5509T>C | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45658115 | |||||||
| chr11:45658116 | G | A | 1 | a0001c0001t0001g0106 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.-226-5510C>T | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45658116 | |||||||
| chr11:45658201 | G | A | 1 | a0001c0001t0001g0107 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-226-5595C>T | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45658201 | |||||||
| chr11:45658239 | T | A | 1 | a0001c0001t0001g0128 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.-226-5633A>T | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45658239 | |||||||
| chr11:45658247 | A | C | 1 | a0001c0001t0001g0128 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.-226-5641T>G | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45658247 | |||||||
| chr11:45658263 | C | G | 1 | a0001c0001t0001g0095 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.-226-5657G>C | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45658263 | |||||||
| chr11:45658443 | G | A | 126 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0016 others(123): Show |
383 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(380): Show |
intron_variant | MODIFIER | c.-226-5837C>T | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45658443 | |||||||
| chr11:45658462 | C | T | 1 | a0001c0001t0001g0094 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-226-5856G>A | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45658462 | |||||||
| chr11:45658569 | G | A | 2 | a0001c0002t0015g0044 a0001c0002t0015g0045 |
2 | HG02258.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.-226-5963C>T | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45658569 | |||||||
| chr11:45658582 | G | T | 1 | a0001c0002t0006g0071 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-226-5976C>A | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45658582 | |||||||
| chr11:45658644 | C | G | 1 | a0001c0001t0001g0030 | 2 | HG02280.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-226-6038G>C | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45658644 | |||||||
| chr11:45658660 | G | A | 66 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0016 others(63): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.-226-6054C>T | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45658660 | |||||||
| chr11:45658699 | G | A | 1 | a0001c0001t0001g0034 | 2 | HG02027.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.-226-6093C>T | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45658699 | |||||||
| chr11:45658736 | T | C | 121 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0016 others(118): Show |
375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): Show |
intron_variant | MODIFIER | c.-226-6130A>G | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45658736 | |||||||
| chr11:45658783 | C | A | 1 | a0001c0001t0002g0055 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.-226-6177G>T | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45658783 | |||||||
| chr11:45658806 | C | T | 1 | a0001c0001t0002g0023 | 2 | HG02071.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.-226-6200G>A | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45658806 | |||||||
| chr11:45658917 | C | G | 1 | a0001c0001t0001g0093 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.-227+6261G>C | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45658917 | |||||||
| chr11:45658956 | G | A | 1 | a0001c0002t0033g0076 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-227+6222C>T | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45658956 | |||||||
| chr11:45658993 | C | A | 1 | a0001c0002t0003g0123 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-227+6185G>T | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45658993 | |||||||
| chr11:45659019 | G | A | 4 | a0001c0002t0004g0007 a0001c0002t0004g0013 a0001c0002t0004g0015 others(1): Show |
13 | HG01884.hp1 HG02145.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.-227+6159C>T | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45659019 | |||||||
| chr11:45659061 | G | A | 1 | a0001c0002t0010g0060 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-227+6117C>T | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45659061 | |||||||
| chr11:45659099 | C | T | 4 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0091 others(1): Show |
8 | HG01167.hp1 HG01346.hp2 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.-227+6079G>A | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45659099 | |||||||
| chr11:45659117 | A | T | 1 | a0001c0001t0011g0037 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-227+6061T>A | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45659117 | |||||||
| chr11:45659129 | G | T | 1 | a0001c0002t0003g0006 | 6 | NA18946.hp1 NA18993.hp1 NA19007.hp2 others(3): Show |
intron_variant | MODIFIER | c.-227+6049C>A | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45659129 | |||||||
| chr11:45659194 | C | T | 1 | a0001c0001t0001g0087 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-227+5984G>A | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45659194 | |||||||
| chr11:45659381 | G | A | 118 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0016 others(115): Show |
372 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(369): Show |
intron_variant | MODIFIER | c.-227+5797C>T | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45659381 | |||||||
| chr11:45659381 | G | C | 1 | a0001c0001t0001g0128 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.-227+5797C>G | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45659381 | |||||||
| chr11:45659413 | C | T | 2 | a0001c0002t0005g0005 a0001c0002t0010g0074 |
9 | HG01109.hp2 HG01884.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.-227+5765G>A | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45659413 | |||||||
| chr11:45659435 | C | T | 7 | a0001c0002t0012g0026 a0001c0002t0012g0062 a0001c0002t0016g0027 others(4): Show |
9 | HG01496.hp1 HG02486.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.-227+5743G>A | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45659435 | |||||||
| chr11:45659468 | A | C | 1 | a0001c0001t0001g0128 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.-227+5710T>G | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45659468 | |||||||
| chr11:45659469 | T | A | 1 | a0001c0001t0001g0128 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.-227+5709A>T | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45659469 | |||||||
| chr11:45659470 | C | T | 1 | a0001c0001t0001g0128 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.-227+5708G>A | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45659470 | |||||||
| chr11:45659700 | C | T | 1 | a0001c0001t0001g0016 | 3 | HG02451.hp2 HG02647.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.-227+5478G>A | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45659700 | |||||||
| chr11:45659779 | T | C | 1 | a0001c0001t0001g0108 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-227+5399A>G | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45659779 | |||||||
| chr11:45659804 | C | A | 121 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0016 others(118): Show |
375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): Show |
intron_variant | MODIFIER | c.-227+5374G>T | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45659804 | |||||||
| chr11:45659862 | C | CTCTCTGC others(7): Show |
1 | a0001c0001t0001g0111 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.-227+5302_-227+531 others(18): Show |
CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45659862 | |||||||
| chr11:45659985 | G | A | 1 | a0001c0002t0003g0003 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-227+5193C>T | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45659985 | |||||||
| chr11:45660025 | G | A | 2 | a0001c0002t0015g0044 a0001c0002t0015g0045 |
2 | HG02258.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.-227+5153C>T | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45660025 | |||||||
| chr11:45660078 | T | C | 1 | a0001c0002t0033g0076 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-227+5100A>G | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45660078 | |||||||
| chr11:45660098 | T | G | 1 | a0001c0001t0014g0109 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-227+5080A>C | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45660098 | |||||||
| chr11:45660194 | T | C | 7 | a0001c0002t0004g0007 a0001c0002t0004g0013 a0001c0002t0004g0015 others(4): Show |
16 | HG01109.hp1 HG01884.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.-227+4984A>G | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45660194 | |||||||
| chr11:45660277 | C | A | 1 | a0001c0001t0001g0110 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.-227+4901G>T | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45660277 | |||||||
| chr11:45660423 | C | A | 1 | a0001c0001t0002g0057 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-227+4755G>T | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45660423 | |||||||
| chr11:45660722 | C | A | 1 | a0001c0001t0001g0111 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.-227+4456G>T | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45660722 | |||||||
| chr11:45660767 | A | G | 4 | a0001c0001t0002g0073 a0001c0001t0010g0072 a0001c0002t0005g0069 others(1): Show |
7 | HG02451.hp1 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.-227+4411T>C | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45660767 | |||||||
| chr11:45661015 | T | A | 1 | a0001c0001t0001g0112 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-227+4163A>T | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45661015 | |||||||
| chr11:45661279 | G | C | 70 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0016 others(67): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.-227+3899C>G | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45661279 | |||||||
| chr11:45661319 | G | A | 1 | a0001c0002t0003g0124 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-227+3859C>T | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45661319 | |||||||
| chr11:45661502 | T | C | 1 | a0001c0002t0030g0077 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-227+3676A>G | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45661502 | |||||||
| chr11:45661838 | C | T | 1 | a0001c0001t0014g0090 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.-227+3340G>A | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45661838 | |||||||
| chr11:45661851 | C | T | 4 | a0001c0002t0008g0008 a0001c0002t0008g0042 a0001c0002t0021g0036 others(1): Show |
7 | HG00140.hp2 HG00280.hp2 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.-227+3327G>A | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45661851 | |||||||
| chr11:45662015 | G | C | 2 | a0001c0001t0011g0037 a0001c0001t0011g0038 |
2 | HG02895.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.-227+3163C>G | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45662015 | |||||||
| chr11:45662041 | A | C | 1 | a0001c0002t0006g0071 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-227+3137T>G | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45662041 | |||||||
| chr11:45662149 | T | A | 1 | a0001c0001t0001g0128 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.-227+3029A>T | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45662149 | |||||||
| chr11:45662259 | G | A | 1 | a0001c0002t0015g0044 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-227+2919C>T | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45662259 | |||||||
| chr11:45662288 | C | A | 2 | a0001c0002t0006g0011 a0001c0002t0006g0070 |
5 | HG01243.hp2 HG02630.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.-227+2890G>T | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45662288 | |||||||
| chr11:45662319 | G | A | 122 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0016 others(119): Show |
376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.-227+2859C>T | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45662319 | |||||||
| chr11:45662418 | A | T | 1 | a0001c0002t0003g0003 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.-227+2760T>A | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45662418 | |||||||
| chr11:45662466 | G | T | 1 | a0001c0001t0009g0049 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-227+2712C>A | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45662466 | |||||||
| chr11:45662483 | C | G | 2 | a0001c0001t0011g0037 a0001c0001t0011g0038 |
2 | HG02895.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.-227+2695G>C | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45662483 | |||||||
| chr11:45662489 | G | C | 2 | a0001c0002t0015g0044 a0001c0002t0015g0045 |
2 | HG02258.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.-227+2689C>G | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45662489 | |||||||
| chr11:45662567 | G | T | 43 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0016 others(40): Show |
143 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.-227+2611C>A | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45662567 | |||||||
| chr11:45662689 | A | G | 1 | a0001c0001t0001g0089 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.-227+2489T>C | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45662689 | |||||||
| chr11:45662704 | C | T | 66 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0016 others(63): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.-227+2474G>A | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45662704 | |||||||
| chr11:45662720 | A | G | 1 | a0001c0001t0001g0088 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-227+2458T>C | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45662720 | |||||||
| chr11:45662787 | G | A | 1 | a0001c0002t0003g0035 | 2 | HG02074.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.-227+2391C>T | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45662787 | |||||||
| chr11:45662878 | T | C | 122 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0016 others(119): Show |
376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.-227+2300A>G | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45662878 | |||||||
| chr11:45662936 | C | T | 54 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0010 others(51): Show |
143 | HG00323.hp1 HG00408.hp1 HG00597.hp2 others(140): Show |
intron_variant | MODIFIER | c.-227+2242G>A | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45662936 | |||||||
| chr11:45663007 | C | T | 122 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0016 others(119): Show |
376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.-227+2171G>A | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45663007 | |||||||
| chr11:45663108 | A | G | 122 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0016 others(119): Show |
376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.-227+2070T>C | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45663108 | |||||||
| chr11:45663280 | C | T | 1 | a0001c0001t0002g0048 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.-227+1898G>A | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45663280 | |||||||
| chr11:45663314 | C | T | 4 | a0001c0001t0001g0014 a0001c0001t0001g0030 a0001c0001t0001g0082 others(1): Show |
8 | HG01243.hp1 HG02280.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.-227+1864G>A | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45663314 | |||||||
| chr11:45663315 | G | A | 1 | a0001c0001t0001g0125 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-227+1863C>T | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45663315 | |||||||
| chr11:45663350 | T | G | 1 | a0001c0002t0010g0074 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-227+1828A>C | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45663350 | |||||||
| chr11:45663363 | G | T | 2 | a0001c0002t0015g0044 a0001c0002t0015g0045 |
2 | HG02258.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.-227+1815C>A | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45663363 | |||||||
| chr11:45663374 | G | A | 3 | a0001c0001t0002g0025 a0001c0001t0002g0057 a0001c0001t0009g0056 |
4 | HG00639.hp1 HG01516.hp1 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.-227+1804C>T | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45663374 | |||||||
| chr11:45663465 | T | C | 4 | a0001c0002t0004g0007 a0001c0002t0004g0013 a0001c0002t0004g0015 others(1): Show |
13 | HG01884.hp1 HG02145.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.-227+1713A>G | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45663465 | |||||||
| chr11:45663503 | C | T | 1 | a0001c0001t0011g0039 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-227+1675G>A | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45663503 | |||||||
| chr11:45663597 | T | A | 1 | a0001c0001t0001g0126 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.-227+1581A>T | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45663597 | |||||||
| chr11:45663640 | G | T | 1 | a0001c0001t0001g0086 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-227+1538C>A | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45663640 | |||||||
| chr11:45663769 | C | T | 7 | a0001c0002t0004g0007 a0001c0002t0004g0013 a0001c0002t0004g0015 others(4): Show |
16 | HG01109.hp1 HG01884.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.-227+1409G>A | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45663769 | |||||||
| chr11:45663811 | C | G | 1 | a0001c0002t0003g0085 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.-227+1367G>C | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45663811 | |||||||
| chr11:45663978 | A | G | 1 | a0001c0002t0004g0015 | 3 | HG01884.hp1 HG03209.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-227+1200T>C | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45663978 | |||||||
| chr11:45664090 | C | T | 1 | a0001c0001t0001g0084 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-227+1088G>A | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45664090 | |||||||
| chr11:45664289 | A | G | 122 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0016 others(119): Show |
376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.-227+889T>C | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45664289 | |||||||
| chr11:45664338 | G | A | 3 | a0001c0001t0002g0073 a0001c0001t0010g0072 a0001c0002t0006g0012 |
6 | HG02451.hp1 HG02486.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-227+840C>T | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45664338 | |||||||
| chr11:45664356 | C | T | 54 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0010 others(51): Show |
143 | HG00323.hp1 HG00408.hp1 HG00597.hp2 others(140): Show |
intron_variant | MODIFIER | c.-227+822G>A | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45664356 | |||||||
| chr11:45664378 | C | T | 1 | a0001c0001t0002g0022 | 2 | NA19007.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.-227+800G>A | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45664378 | |||||||
| chr11:45664457 | C | G | 1 | a0001c0002t0039g0083 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-227+721G>C | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45664457 | |||||||
| chr11:45664469 | C | T | 1 | a0001c0001t0002g0047 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-227+709G>A | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45664469 | |||||||
| chr11:45664530 | T | C | 1 | a0001c0002t0010g0074 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-227+648A>G | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45664530 | |||||||
| chr11:45664541 | ACCGCGAA others(13): Show |
A | 1 | a0001c0001t0002g0046 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-227+617_-227+636d others(22): Show |
CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45664541 | |||||||
| chr11:45664628 | C | G | 1 | a0001c0001t0002g0046 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-227+550G>C | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45664628 | |||||||
| chr11:45664629 | T | C | 1 | a0001c0001t0002g0046 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-227+549A>G | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45664629 | |||||||
| chr11:45664675 | G | C | 4 | a0001c0002t0008g0008 a0001c0002t0008g0042 a0001c0002t0021g0036 others(1): Show |
7 | HG00140.hp2 HG00280.hp2 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.-227+503C>G | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45664675 | |||||||
| chr11:45664714 | C | A | 1 | a0001c0001t0001g0127 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.-227+464G>T | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45664714 | |||||||
| chr11:45664728 | A | T | 1 | a0001c0001t0002g0046 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-227+450T>A | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45664728 | |||||||
| chr11:45664732 | A | G | 1 | a0001c0001t0002g0046 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-227+446T>C | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45664732 | |||||||
| chr11:45664735 | A | G | 38 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0010 others(35): Show |
115 | HG00323.hp1 HG00408.hp1 HG00597.hp2 others(112): Show |
intron_variant | MODIFIER | c.-227+443T>C | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45664735 | |||||||
| chr11:45664741 | C | G | 1 | a0001c0001t0002g0046 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-227+437G>C | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45664741 | |||||||
| chr11:45664747 | C | G | 1 | a0001c0001t0002g0046 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-227+431G>C | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45664747 | |||||||
| chr11:45664774 | G | T | 2 | a0001c0002t0010g0059 a0001c0002t0010g0060 |
2 | HG02970.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-227+404C>A | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45664774 | |||||||
| chr11:45664792 | G | T | 1 | a0001c0001t0001g0082 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-227+386C>A | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45664792 | |||||||
| chr11:45664849 | G | A | 1 | a0001c0002t0008g0042 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-227+329C>T | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45664849 | |||||||
| chr11:45664921 | T | G | 1 | a0001c0001t0001g0128 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.-227+257A>C | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45664921 | |||||||
| chr11:45664923 | T | G | 1 | a0001c0001t0001g0128 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.-227+255A>C | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45664923 | |||||||
| chr11:45664930 | T | G | 1 | a0001c0001t0001g0128 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.-227+248A>C | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45664930 | |||||||
| chr11:45664934 | G | C | 1 | a0001c0001t0001g0128 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.-227+244C>G | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45664934 | |||||||
| chr11:45664962 | T | C | 7 | a0001c0002t0004g0007 a0001c0002t0004g0013 a0001c0002t0004g0015 others(4): Show |
16 | HG01109.hp1 HG01884.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.-227+216A>G | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45664962 | |||||||
| chr11:45664983 | C | G | 54 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0010 others(51): Show |
143 | HG00323.hp1 HG00408.hp1 HG00597.hp2 others(140): Show |
intron_variant | MODIFIER | c.-227+195G>C | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45664983 | |||||||
| chr11:45665005 | C | T | 19 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0010 others(16): Show |
82 | HG00323.hp1 HG00408.hp1 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.-227+173G>A | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45665005 | |||||||
| chr11:45665144 | G | A | 54 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0010 others(51): Show |
143 | HG00323.hp1 HG00408.hp1 HG00597.hp2 others(140): Show |
intron_variant | MODIFIER | c.-227+34C>T | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45665144 | |||||||
| chr11:45665162 | G | C | 1 | a0001c0002t0021g0036 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.-227+16C>G | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45665162 | |||||||
| chr11:45665169 | G | A | 1 | a0001c0002t0015g0045 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-227+9C>T | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45665169 | |||||||
| chr11:45665169 | G | C | 1 | a0001c0002t0021g0036 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.-227+9C>G | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45665169 | |||||||
| chr11:45665175 | T | G | 1 | a0001c0002t0021g0036 | 1 | HG01257.hp2 | splice_region_variant&intron_variant | LOW | c.-227+3A>C | CHST1 | ENSG00000175264.8 | transcript | ENST00000308064.7 | protein_coding | 1/3 | chr11 | 45665175 |