Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 9486 |
| ensemblid | ENSG00000115526.11 |
| hgncid | 19650 |
| symbol | CHST10 |
| name | carbohydrate sulfotransferase 10 |
| refseq_nuc | NM_004854.5 |
| refseq_prot | NP_004845.1 |
| ensembl_nuc | ENST00000264249.8 |
| ensembl_prot | ENSP00000264249.3 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 100391860 |
| end | 100417668 |
| strand | - |
| ver | v1.2 |
| region | chr2:100391860-100417668 |
| region5000 | chr2:100386860-100422668 |
| regionname0 | CHST10_chr2_100391860_100417668 |
| regionname5000 | CHST10_chr2_100386860_100422668 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 356 | 345 | 78 | 69 | 142 | 14 | 40 | 104 | CHST10_chr2_100386860_100422668 | CHST10 | MHHQW others(351): Show |
chr2 | 100386860 | 100422668 |
| a0002 | 0/0 | 356 | 9 | 9 | 0 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | MHHQW others(351): Show |
chr2 | 100386860 | 100422668 |
| a0003 | 0/0 | 356 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | MHHQW others(351): Show |
chr2 | 100386860 | 100422668 |
| a0004 | 0/0 | 356 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | MHHQW others(351): Show |
chr2 | 100386860 | 100422668 |
| a0005 | 0/0 | 356 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | MHHQW others(351): Show |
chr2 | 100386860 | 100422668 |
| a0006 | 0/0 | 356 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | MHHQW others(351): Show |
chr2 | 100386860 | 100422668 |
| a0007 | 0/0 | 356 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | MHHQW others(351): Show |
chr2 | 100386860 | 100422668 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1068 | 188 | 53 | 34 | 76 | 8 | 16 | CHST10_chr2_100386860_100422668 | CHST10 | ATGCA others(1063): Show |
chr2 | 100386860 | 100422668 | ||
| a0001c0002 | 1/0 | 1068 | 123 | 22 | 35 | 37 | 6 | 22 | CHST10_chr2_100386860_100422668 | CHST10 | ATGCA others(1063): Show |
chr2 | 100386860 | 100422668 | ||
| a0001c0003 | 0/0 | 1068 | 11 | 0 | 0 | 11 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | ATGCA others(1063): Show |
chr2 | 100386860 | 100422668 | ||
| a0001c0004 | 0/0 | 1068 | 9 | 0 | 0 | 9 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | ATGCA others(1063): Show |
chr2 | 100386860 | 100422668 | ||
| a0001c0006 | 0/0 | 1068 | 5 | 0 | 0 | 4 | 0 | 1 | CHST10_chr2_100386860_100422668 | CHST10 | ATGCA others(1063): Show |
chr2 | 100386860 | 100422668 | ||
| a0001c0007 | 0/0 | 1068 | 5 | 0 | 0 | 5 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | ATGCA others(1063): Show |
chr2 | 100386860 | 100422668 | ||
| a0001c0011 | 0/0 | 1068 | 2 | 2 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | ATGCA others(1063): Show |
chr2 | 100386860 | 100422668 | ||
| a0001c0014 | 0/0 | 1068 | 1 | 1 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | ATGCA others(1063): Show |
chr2 | 100386860 | 100422668 | ||
| a0001c0016 | 0/0 | 1068 | 1 | 0 | 0 | 0 | 0 | 1 | CHST10_chr2_100386860_100422668 | CHST10 | ATGCA others(1063): Show |
chr2 | 100386860 | 100422668 | ||
| a0002c0005 | 0/0 | 1068 | 7 | 7 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | ATGCA others(1063): Show |
chr2 | 100386860 | 100422668 | ||
| a0002c0009 | 0/0 | 1068 | 2 | 2 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | ATGCA others(1063): Show |
chr2 | 100386860 | 100422668 | ||
| a0003c0008 | 0/0 | 1068 | 5 | 5 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | ATGCA others(1063): Show |
chr2 | 100386860 | 100422668 | ||
| a0004c0010 | 0/0 | 1068 | 2 | 2 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | ATGCA others(1063): Show |
chr2 | 100386860 | 100422668 | ||
| a0005c0012 | 0/0 | 1068 | 1 | 0 | 1 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | ATGCA others(1063): Show |
chr2 | 100386860 | 100422668 | ||
| a0006c0015 | 0/0 | 1068 | 1 | 1 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | ATGCA others(1063): Show |
chr2 | 100386860 | 100422668 | ||
| a0007c0013 | 0/0 | 1068 | 1 | 1 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | ATGCA others(1063): Show |
chr2 | 100386860 | 100422668 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002 | 0/1 | 2854 | 86 | 1 | 20 | 50 | 7 | 7 | CHST10_chr2_100386860_100422668 | CHST10 | AGGCG others(2849): Show |
chr2 | 100386860 | 100422668 |
| a0001c0001t0003 | 0/0 | 2854 | 28 | 11 | 9 | 0 | 0 | 8 | CHST10_chr2_100386860_100422668 | CHST10 | AGGCG others(2849): Show |
chr2 | 100386860 | 100422668 |
| a0001c0001t0004 | 0/0 | 2854 | 21 | 20 | 0 | 0 | 1 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | AGGCG others(2849): Show |
chr2 | 100386860 | 100422668 |
| a0001c0001t0005 | 0/0 | 2854 | 18 | 12 | 3 | 3 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | AGGCG others(2849): Show |
chr2 | 100386860 | 100422668 |
| a0001c0001t0006 | 0/0 | 2854 | 12 | 6 | 0 | 6 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | AGGCG others(2849): Show |
chr2 | 100386860 | 100422668 |
| a0001c0001t0008 | 0/0 | 2854 | 9 | 0 | 0 | 9 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | AGGCG others(2849): Show |
chr2 | 100386860 | 100422668 |
| a0001c0001t0011 | 0/0 | 2854 | 2 | 0 | 0 | 2 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | AGGCG others(2849): Show |
chr2 | 100386860 | 100422668 |
| a0001c0001t0012 | 0/0 | 2854 | 2 | 0 | 2 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | AGGCG others(2849): Show |
chr2 | 100386860 | 100422668 |
| a0001c0001t0013 | 0/0 | 2854 | 2 | 0 | 0 | 2 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | AGGCG others(2849): Show |
chr2 | 100386860 | 100422668 |
| a0001c0001t0016 | 0/0 | 2854 | 2 | 2 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | AGGCG others(2849): Show |
chr2 | 100386860 | 100422668 |
| a0001c0001t0017 | 0/0 | 2854 | 1 | 0 | 0 | 1 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | AGGCG others(2849): Show |
chr2 | 100386860 | 100422668 |
| a0001c0001t0018 | 0/0 | 2854 | 1 | 0 | 0 | 1 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | AGGCG others(2849): Show |
chr2 | 100386860 | 100422668 |
| a0001c0001t0019 | 0/0 | 2854 | 1 | 0 | 0 | 0 | 0 | 1 | CHST10_chr2_100386860_100422668 | CHST10 | AGGCG others(2849): Show |
chr2 | 100386860 | 100422668 |
| a0001c0001t0023 | 0/0 | 2854 | 1 | 0 | 0 | 1 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | AGGCG others(2849): Show |
chr2 | 100386860 | 100422668 |
| a0001c0001t0024 | 0/0 | 2854 | 1 | 0 | 0 | 1 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | AGGCG others(2849): Show |
chr2 | 100386860 | 100422668 |
| a0001c0001t0029 | 0/0 | 2854 | 1 | 1 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | AGGCG others(2849): Show |
chr2 | 100386860 | 100422668 |
| a0001c0002t0001 | 1/0 | 2854 | 116 | 22 | 33 | 36 | 5 | 19 | CHST10_chr2_100386860_100422668 | CHST10 | AGGCG others(2849): Show |
chr2 | 100386860 | 100422668 |
| a0001c0002t0014 | 0/0 | 2854 | 2 | 0 | 0 | 0 | 0 | 2 | CHST10_chr2_100386860_100422668 | CHST10 | AGGCG others(2849): Show |
chr2 | 100386860 | 100422668 |
| a0001c0002t0015 | 0/0 | 2854 | 2 | 0 | 0 | 0 | 1 | 1 | CHST10_chr2_100386860_100422668 | CHST10 | AGGCG others(2849): Show |
chr2 | 100386860 | 100422668 |
| a0001c0002t0020 | 0/0 | 2854 | 1 | 0 | 0 | 1 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | AGGCG others(2849): Show |
chr2 | 100386860 | 100422668 |
| a0001c0002t0021 | 0/0 | 2854 | 1 | 0 | 1 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | AGGCG others(2849): Show |
chr2 | 100386860 | 100422668 |
| a0001c0002t0026 | 0/0 | 2854 | 1 | 0 | 1 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | AGGCG others(2849): Show |
chr2 | 100386860 | 100422668 |
| a0001c0003t0007 | 0/0 | 2854 | 11 | 0 | 0 | 11 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | AGGCG others(2849): Show |
chr2 | 100386860 | 100422668 |
| a0001c0004t0002 | 0/0 | 2854 | 8 | 0 | 0 | 8 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | AGGCG others(2849): Show |
chr2 | 100386860 | 100422668 |
| a0001c0004t0025 | 0/0 | 2854 | 1 | 0 | 0 | 1 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | AGGCG others(2849): Show |
chr2 | 100386860 | 100422668 |
| a0001c0006t0002 | 0/0 | 2854 | 5 | 0 | 0 | 4 | 0 | 1 | CHST10_chr2_100386860_100422668 | CHST10 | AGGCG others(2849): Show |
chr2 | 100386860 | 100422668 |
| a0001c0007t0003 | 0/0 | 2854 | 5 | 0 | 0 | 5 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | AGGCG others(2849): Show |
chr2 | 100386860 | 100422668 |
| a0001c0011t0005 | 0/0 | 2854 | 1 | 1 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | AGGCG others(2849): Show |
chr2 | 100386860 | 100422668 |
| a0001c0011t0006 | 0/0 | 2854 | 1 | 1 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | AGGCG others(2849): Show |
chr2 | 100386860 | 100422668 |
| a0001c0014t0004 | 0/0 | 2854 | 1 | 1 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | AGGCG others(2849): Show |
chr2 | 100386860 | 100422668 |
| a0001c0016t0002 | 0/0 | 2854 | 1 | 0 | 0 | 0 | 0 | 1 | CHST10_chr2_100386860_100422668 | CHST10 | AGGCG others(2849): Show |
chr2 | 100386860 | 100422668 |
| a0002c0005t0009 | 0/0 | 2854 | 3 | 3 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | AGGCG others(2849): Show |
chr2 | 100386860 | 100422668 |
| a0002c0005t0010 | 0/0 | 2854 | 2 | 2 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | AGGCG others(2849): Show |
chr2 | 100386860 | 100422668 |
| a0002c0005t0022 | 0/0 | 2854 | 1 | 1 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | AGGCG others(2849): Show |
chr2 | 100386860 | 100422668 |
| a0002c0005t0027 | 0/0 | 2854 | 1 | 1 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | AGGCG others(2849): Show |
chr2 | 100386860 | 100422668 |
| a0002c0009t0001 | 0/0 | 2854 | 2 | 2 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | AGGCG others(2849): Show |
chr2 | 100386860 | 100422668 |
| a0003c0008t0003 | 0/0 | 2854 | 5 | 5 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | AGGCG others(2849): Show |
chr2 | 100386860 | 100422668 |
| a0004c0010t0005 | 0/0 | 2854 | 2 | 2 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | AGGCG others(2849): Show |
chr2 | 100386860 | 100422668 |
| a0005c0012t0003 | 0/0 | 2854 | 1 | 0 | 1 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | AGGCG others(2849): Show |
chr2 | 100386860 | 100422668 |
| a0006c0015t0004 | 0/0 | 2854 | 1 | 1 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | AGGCG others(2849): Show |
chr2 | 100386860 | 100422668 |
| a0007c0013t0028 | 0/0 | 2854 | 1 | 1 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | AGGCG others(2849): Show |
chr2 | 100386860 | 100422668 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002g0001 | 0/0 | 27 | 0 | 6 | 17 | 1 | 3 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0001t0002g0009 | 0/0 | 7 | 0 | 7 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0001t0002g0021 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0001t0002g0029 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0001t0002g0030 | 0/0 | 3 | 0 | 0 | 0 | 2 | 1 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0001t0002g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0001t0002g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0001t0002g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0001t0002g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0001t0002g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0001t0002g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0001t0002g0157 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0001t0003g0005 | 0/0 | 11 | 6 | 0 | 0 | 0 | 5 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0001t0003g0007 | 0/0 | 9 | 0 | 9 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0001t0003g0023 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0001t0003g0024 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0001t0003g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0001t0003g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0001t0004g0004 | 0/0 | 12 | 12 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0001t0004g0028 | 0/0 | 3 | 2 | 0 | 0 | 1 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0001t0004g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0001t0004g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0001t0004g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0001t0004g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0001t0005g0015 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0001t0005g0016 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0001t0005g0022 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0001t0005g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0001t0005g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0001t0005g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0001t0005g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0001t0005g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0001t0005g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0001t0005g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0001t0006g0012 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0001t0006g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0001t0006g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0001t0006g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0001t0006g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0001t0006g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0001t0006g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0001t0008g0014 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0001t0008g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0001t0008g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0001t0008g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0001t0008g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0001t0011g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0001t0012g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0001t0012g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0001t0013g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0001t0016g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0001t0017g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0001t0018g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0001t0019g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0001t0023g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0001t0024g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0001t0029g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0002t0001g0002 | 0/0 | 22 | 0 | 5 | 14 | 1 | 2 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0002t0001g0003 | 0/0 | 17 | 5 | 4 | 5 | 0 | 3 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0002t0001g0006 | 0/0 | 10 | 0 | 8 | 0 | 2 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0002t0001g0011 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0002t0001g0019 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0002t0001g0020 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0002t0001g0025 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0002t0001g0026 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0002t0001g0027 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0002t0001g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0002t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0002t0001g0039 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0002t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0002t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0002t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0002t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0002t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0002t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0002t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0002t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0002t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0002t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0002t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0002t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0002t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0002t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0002t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0002t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0002t0001g0168 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0002t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0002t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0002t0014g0038 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0002t0015g0036 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0002t0020g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0002t0021g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0002t0026g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0003t0007g0008 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0003t0007g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0003t0007g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0004t0002g0010 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0004t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0004t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0004t0025g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0006t0002g0013 | 0/0 | 5 | 0 | 0 | 4 | 0 | 1 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0007t0003g0018 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0007t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0011t0005g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0011t0006g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0014t0004g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0001c0016t0002g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0002c0005t0009g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0002c0005t0009g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0002c0005t0010g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0002c0005t0010g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0002c0005t0022g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0002c0005t0027g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0002c0009t0001g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0003c0008t0003g0017 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0003c0008t0003g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0004c0010t0005g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0005c0012t0003g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0006c0015t0004g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| a0007c0013t0028g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0002 | t0001 | g0103 | EUR | GBR | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0001 | EUR | GBR | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG00280 | hp1 | a0001 | c0002 | t0001 | g0006 | EUR | FIN | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0030 | EUR | FIN | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG00323 | hp1 | a0001 | c0002 | t0015 | g0036 | EUR | FIN | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0158 | EUR | FIN | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG00423 | hp1 | a0001 | c0003 | t0007 | g0008 | EAS | CHS | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0029 | EAS | CHS | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG00438 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | CHS | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG00438 | hp2 | a0001 | c0001 | t0024 | g0148 | EAS | CHS | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG00544 | hp1 | a0001 | c0006 | t0002 | g0013 | EAS | CHS | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG00544 | hp2 | a0001 | c0003 | t0007 | g0008 | EAS | CHS | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0160 | EAS | CHS | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | CHS | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG00597 | hp2 | a0001 | c0001 | t0006 | g0012 | EAS | CHS | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG00609 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | CHS | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG00609 | hp2 | a0001 | c0004 | t0002 | g0010 | EAS | CHS | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG00621 | hp2 | a0001 | c0006 | t0002 | g0013 | EAS | CHS | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG00639 | hp1 | a0001 | c0002 | t0001 | g0006 | AMR | PUR | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0009 | AMR | PUR | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG00642 | hp1 | a0001 | c0002 | t0001 | g0019 | AMR | PUR | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG00735 | hp1 | a0001 | c0001 | t0003 | g0007 | AMR | PUR | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG00735 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG00738 | hp2 | a0001 | c0002 | t0001 | g0104 | AMR | PUR | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG00741 | hp2 | a0001 | c0001 | t0003 | g0007 | AMR | PUR | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG01071 | hp1 | a0001 | c0002 | t0001 | g0003 | AMR | PUR | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG01081 | hp1 | a0001 | c0002 | t0026 | g0109 | AMR | PUR | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG01099 | hp1 | a0001 | c0002 | t0001 | g0027 | AMR | PUR | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG01099 | hp2 | a0001 | c0002 | t0001 | g0006 | AMR | PUR | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG01106 | hp1 | a0001 | c0002 | t0001 | g0006 | AMR | PUR | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG01106 | hp2 | a0001 | c0002 | t0001 | g0087 | AMR | PUR | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0125 | AMR | PUR | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG01167 | hp2 | a0001 | c0001 | t0005 | g0016 | AMR | PUR | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG01168 | hp1 | a0001 | c0002 | t0001 | g0006 | AMR | PUR | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG01168 | hp2 | a0001 | c0002 | t0001 | g0025 | AMR | PUR | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG01169 | hp1 | a0001 | c0002 | t0001 | g0025 | AMR | PUR | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0124 | AMR | PUR | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG01175 | hp1 | a0001 | c0002 | t0001 | g0027 | AMR | PUR | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG01175 | hp2 | a0001 | c0002 | t0001 | g0167 | AMR | PUR | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG01192 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG01192 | hp2 | a0001 | c0001 | t0012 | g0127 | AMR | PUR | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG01243 | hp1 | a0005 | c0012 | t0003 | g0069 | AMR | PUR | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG01243 | hp2 | a0001 | c0001 | t0003 | g0007 | AMR | PUR | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG01255 | hp1 | a0001 | c0002 | t0001 | g0106 | AMR | CLM | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG01255 | hp2 | a0001 | c0002 | t0001 | g0166 | AMR | CLM | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG01256 | hp2 | a0001 | c0002 | t0001 | g0006 | AMR | CLM | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG01257 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | CLM | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0137 | AMR | CLM | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG01258 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | CLM | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG01258 | hp2 | a0001 | c0002 | t0001 | g0006 | AMR | CLM | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG01261 | hp1 | a0001 | c0001 | t0012 | g0128 | AMR | CLM | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG01261 | hp2 | a0001 | c0001 | t0005 | g0015 | AMR | CLM | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG01346 | hp1 | a0001 | c0002 | t0001 | g0003 | AMR | CLM | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0164 | AMR | CLM | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG01358 | hp1 | a0001 | c0002 | t0001 | g0003 | AMR | CLM | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG01358 | hp2 | a0001 | c0002 | t0021 | g0054 | AMR | CLM | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG01361 | hp1 | a0001 | c0001 | t0003 | g0007 | AMR | CLM | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG01361 | hp2 | a0001 | c0002 | t0001 | g0006 | AMR | CLM | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG01496 | hp1 | a0001 | c0002 | t0001 | g0019 | AMR | CLM | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG01496 | hp2 | a0001 | c0002 | t0001 | g0003 | AMR | CLM | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0153 | EUR | IBS | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0152 | EUR | IBS | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG01516 | hp1 | a0001 | c0001 | t0004 | g0028 | EUR | IBS | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0154 | EUR | IBS | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG01884 | hp1 | a0001 | c0001 | t0006 | g0079 | AFR | ACB | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG01884 | hp2 | a0001 | c0002 | t0001 | g0099 | AFR | ACB | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG01891 | hp1 | a0001 | c0001 | t0003 | g0005 | AFR | ACB | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG01891 | hp2 | a0001 | c0001 | t0029 | g0082 | AFR | ACB | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG01928 | hp1 | a0001 | c0002 | t0001 | g0091 | AMR | PEL | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0009 | AMR | PEL | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG01934 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PEL | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG01934 | hp2 | a0001 | c0002 | t0001 | g0019 | AMR | PEL | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG01952 | hp1 | a0001 | c0002 | t0001 | g0112 | AMR | PEL | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0009 | AMR | PEL | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG01975 | hp1 | a0001 | c0001 | t0003 | g0007 | AMR | PEL | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0009 | AMR | PEL | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0147 | AMR | PEL | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0009 | AMR | PEL | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG01981 | hp1 | a0001 | c0001 | t0003 | g0007 | AMR | PEL | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG01981 | hp2 | a0001 | c0002 | t0001 | g0006 | AMR | PEL | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0009 | AMR | PEL | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG01993 | hp2 | a0001 | c0002 | t0001 | g0019 | AMR | PEL | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG02015 | hp1 | a0001 | c0001 | t0023 | g0162 | EAS | KHV | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0142 | EAS | KHV | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG02040 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | KHV | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG02040 | hp2 | a0001 | c0006 | t0002 | g0013 | EAS | KHV | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG02055 | hp1 | a0001 | c0001 | t0004 | g0004 | AFR | ACB | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG02055 | hp2 | a0001 | c0001 | t0005 | g0015 | AFR | ACB | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG02056 | hp1 | a0001 | c0003 | t0007 | g0008 | EAS | KHV | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG02074 | hp1 | a0001 | c0003 | t0007 | g0008 | EAS | KHV | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0140 | EAS | KHV | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0047 | EAS | KHV | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG02080 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | KHV | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG02083 | hp1 | a0001 | c0001 | t0008 | g0014 | EAS | KHV | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG02083 | hp2 | a0001 | c0003 | t0007 | g0008 | EAS | KHV | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0159 | EAS | KHV | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG02129 | hp2 | a0001 | c0001 | t0008 | g0014 | EAS | KHV | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0009 | AMR | PEL | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG02148 | hp2 | a0001 | c0001 | t0005 | g0022 | AMR | PEL | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG02155 | hp1 | a0001 | c0001 | t0008 | g0143 | EAS | CDX | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0029 | EAS | CDX | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG02165 | hp1 | a0001 | c0003 | t0007 | g0008 | EAS | CDX | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CDX | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG02257 | hp1 | a0002 | c0005 | t0022 | g0056 | AFR | ACB | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG02257 | hp2 | a0001 | c0001 | t0006 | g0080 | AFR | ACB | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG02258 | hp1 | a0001 | c0001 | t0005 | g0062 | AFR | ACB | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG02258 | hp2 | a0001 | c0002 | t0001 | g0170 | AFR | ACB | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0144 | AMR | PEL | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG02273 | hp2 | a0001 | c0001 | t0003 | g0007 | AMR | PEL | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG02280 | hp1 | a0003 | c0008 | t0003 | g0070 | AFR | ACB | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG02280 | hp2 | a0001 | c0001 | t0005 | g0015 | AFR | ACB | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG02293 | hp1 | a0001 | c0001 | t0003 | g0007 | AMR | PEL | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0129 | AMR | PEL | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG02300 | hp1 | a0001 | c0001 | t0003 | g0007 | AMR | PEL | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG02300 | hp2 | a0001 | c0002 | t0001 | g0100 | AMR | PEL | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG02451 | hp1 | a0001 | c0002 | t0001 | g0003 | AFR | ACB | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG02451 | hp2 | a0001 | c0001 | t0004 | g0004 | AFR | ACB | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG02572 | hp1 | a0001 | c0002 | t0001 | g0116 | AFR | GWD | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG02572 | hp2 | a0001 | c0002 | t0001 | g0020 | AFR | GWD | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0146 | SAS | PJL | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG02602 | hp2 | a0001 | c0002 | t0001 | g0108 | SAS | PJL | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG02615 | hp1 | a0001 | c0001 | t0004 | g0004 | AFR | GWD | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG02615 | hp2 | a0001 | c0002 | t0001 | g0086 | AFR | GWD | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG02622 | hp1 | a0001 | c0002 | t0001 | g0083 | AFR | GWD | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG02622 | hp2 | a0001 | c0001 | t0005 | g0016 | AFR | GWD | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG02630 | hp1 | a0001 | c0001 | t0003 | g0005 | AFR | GWD | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0155 | AFR | GWD | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG02647 | hp1 | a0001 | c0001 | t0003 | g0073 | AFR | GWD | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG02647 | hp2 | a0004 | c0010 | t0005 | g0032 | AFR | GWD | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0030 | SAS | PJL | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG02683 | hp2 | a0001 | c0002 | t0001 | g0111 | SAS | PJL | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG02698 | hp2 | a0001 | c0002 | t0015 | g0036 | SAS | PJL | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG02717 | hp1 | a0002 | c0005 | t0010 | g0055 | AFR | GWD | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG02717 | hp2 | a0001 | c0002 | t0001 | g0020 | AFR | GWD | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG02723 | hp1 | a0001 | c0001 | t0004 | g0028 | AFR | GWD | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG02723 | hp2 | a0001 | c0001 | t0005 | g0016 | AFR | GWD | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG02735 | hp1 | a0001 | c0002 | t0001 | g0003 | SAS | PJL | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG02735 | hp2 | a0001 | c0001 | t0003 | g0005 | SAS | PJL | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG02738 | hp1 | a0001 | c0002 | t0001 | g0089 | SAS | PJL | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG02738 | hp2 | a0001 | c0016 | t0002 | g0149 | SAS | PJL | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG02809 | hp1 | a0001 | c0002 | t0001 | g0035 | AFR | GWD | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG02809 | hp2 | a0001 | c0014 | t0004 | g0118 | AFR | GWD | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG02818 | hp1 | a0001 | c0001 | t0004 | g0041 | AFR | GWD | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG02818 | hp2 | a0001 | c0001 | t0003 | g0005 | AFR | GWD | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG02895 | hp1 | a0003 | c0008 | t0003 | g0017 | AFR | GWD | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG02895 | hp2 | a0001 | c0001 | t0004 | g0004 | AFR | GWD | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG02896 | hp1 | a0002 | c0009 | t0001 | g0042 | AFR | GWD | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG02896 | hp2 | a0002 | c0005 | t0009 | g0059 | AFR | GWD | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG02897 | hp1 | a0002 | c0009 | t0001 | g0042 | AFR | GWD | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG02897 | hp2 | a0001 | c0001 | t0004 | g0120 | AFR | GWD | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG02922 | hp1 | a0001 | c0001 | t0004 | g0004 | AFR | ESN | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG02922 | hp2 | a0002 | c0005 | t0010 | g0057 | AFR | ESN | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG02965 | hp1 | a0003 | c0008 | t0003 | g0017 | AFR | ESN | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG02965 | hp2 | a0001 | c0002 | t0001 | g0003 | AFR | ESN | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG02970 | hp1 | a0001 | c0001 | t0004 | g0004 | AFR | ESN | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG02970 | hp2 | a0001 | c0011 | t0005 | g0074 | AFR | ESN | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG02976 | hp1 | a0001 | c0002 | t0001 | g0025 | AFR | ESN | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG02976 | hp2 | a0001 | c0002 | t0001 | g0020 | AFR | ESN | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG03041 | hp1 | a0001 | c0002 | t0001 | g0115 | AFR | GWD | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG03041 | hp2 | a0001 | c0001 | t0004 | g0004 | AFR | GWD | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG03098 | hp1 | a0001 | c0001 | t0004 | g0004 | AFR | MSL | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG03098 | hp2 | a0001 | c0002 | t0001 | g0020 | AFR | MSL | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG03130 | hp1 | a0001 | c0001 | t0006 | g0033 | AFR | ESN | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG03130 | hp2 | a0001 | c0001 | t0003 | g0005 | AFR | ESN | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG03139 | hp1 | a0001 | c0001 | t0005 | g0016 | AFR | ESN | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG03139 | hp2 | a0001 | c0001 | t0003 | g0023 | AFR | ESN | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG03195 | hp1 | a0001 | c0001 | t0004 | g0119 | AFR | ESN | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG03195 | hp2 | a0001 | c0001 | t0004 | g0040 | AFR | ESN | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG03209 | hp1 | a0001 | c0001 | t0003 | g0005 | AFR | MSL | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG03209 | hp2 | a0003 | c0008 | t0003 | g0017 | AFR | MSL | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG03225 | hp1 | a0002 | c0005 | t0009 | g0031 | AFR | MSL | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG03225 | hp2 | a0001 | c0001 | t0004 | g0041 | AFR | MSL | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG03239 | hp1 | a0001 | c0002 | t0001 | g0002 | SAS | PJL | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG03453 | hp1 | a0002 | c0005 | t0027 | g0058 | AFR | MSL | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG03453 | hp2 | a0003 | c0008 | t0003 | g0017 | AFR | MSL | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG03486 | hp1 | a0001 | c0001 | t0005 | g0066 | AFR | MSL | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG03486 | hp2 | a0001 | c0001 | t0004 | g0004 | AFR | MSL | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG03490 | hp1 | a0001 | c0002 | t0014 | g0038 | SAS | PJL | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG03490 | hp2 | a0001 | c0002 | t0001 | g0039 | SAS | PJL | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG03491 | hp1 | a0001 | c0002 | t0001 | g0114 | SAS | PJL | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG03491 | hp2 | a0001 | c0001 | t0003 | g0024 | SAS | PJL | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG03492 | hp1 | a0001 | c0002 | t0014 | g0038 | SAS | PJL | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG03492 | hp2 | a0001 | c0001 | t0003 | g0024 | SAS | PJL | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG03516 | hp1 | a0001 | c0002 | t0001 | g0035 | AFR | ESN | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG03516 | hp2 | a0001 | c0002 | t0001 | g0102 | AFR | ESN | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG03540 | hp1 | a0001 | c0002 | t0001 | g0003 | AFR | GWD | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG03540 | hp2 | a0007 | c0013 | t0028 | g0077 | AFR | GWD | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG03579 | hp1 | a0001 | c0001 | t0003 | g0023 | AFR | MSL | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG03579 | hp2 | a0001 | c0001 | t0006 | g0081 | AFR | MSL | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG03654 | hp1 | a0001 | c0002 | t0001 | g0060 | SAS | PJL | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG03654 | hp2 | a0001 | c0001 | t0003 | g0005 | SAS | PJL | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0130 | SAS | PJL | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG03704 | hp1 | a0001 | c0001 | t0003 | g0005 | SAS | PJL | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG03704 | hp2 | a0001 | c0002 | t0001 | g0107 | SAS | PJL | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG03710 | hp1 | a0001 | c0002 | t0001 | g0105 | SAS | PJL | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG03710 | hp2 | a0001 | c0006 | t0002 | g0013 | SAS | PJL | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG03831 | hp1 | a0001 | c0002 | t0001 | g0110 | SAS | BEB | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG03831 | hp2 | a0001 | c0001 | t0003 | g0024 | SAS | BEB | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG03834 | hp1 | a0001 | c0001 | t0003 | g0005 | SAS | BEB | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG03834 | hp2 | a0001 | c0002 | t0001 | g0003 | SAS | BEB | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG03927 | hp1 | a0001 | c0001 | t0003 | g0005 | SAS | BEB | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG03927 | hp2 | a0001 | c0002 | t0001 | g0098 | SAS | BEB | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG03942 | hp1 | a0001 | c0002 | t0001 | g0039 | SAS | BEB | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG03942 | hp2 | a0001 | c0002 | t0001 | g0092 | SAS | BEB | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG04184 | hp1 | a0001 | c0002 | t0001 | g0002 | SAS | BEB | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG04184 | hp2 | a0001 | c0001 | t0019 | g0052 | SAS | BEB | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG04228 | hp1 | a0001 | c0002 | t0001 | g0003 | SAS | STU | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0132 | SAS | STU | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| NA18522 | hp1 | a0002 | c0005 | t0009 | g0031 | AFR | YRI | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| NA18522 | hp2 | a0001 | c0002 | t0001 | g0003 | AFR | YRI | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| NA18612 | hp1 | a0001 | c0001 | t0006 | g0012 | EAS | CHB | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| NA18612 | hp2 | a0001 | c0001 | t0008 | g0123 | EAS | CHB | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHB | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| NA18747 | hp2 | a0001 | c0002 | t0001 | g0093 | EAS | CHB | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| NA18906 | hp1 | a0001 | c0002 | t0001 | g0003 | AFR | YRI | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| NA18906 | hp2 | a0001 | c0001 | t0003 | g0005 | AFR | YRI | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| NA18939 | hp1 | a0001 | c0007 | t0003 | g0018 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| NA18941 | hp1 | a0001 | c0007 | t0003 | g0072 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| NA18944 | hp1 | a0001 | c0001 | t0008 | g0014 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| NA18944 | hp2 | a0001 | c0002 | t0001 | g0085 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| NA18945 | hp2 | a0001 | c0007 | t0003 | g0018 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| NA18948 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| NA18951 | hp1 | a0001 | c0001 | t0006 | g0012 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| NA18951 | hp2 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0131 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| NA18953 | hp2 | a0001 | c0001 | t0005 | g0022 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| NA18954 | hp1 | a0001 | c0007 | t0003 | g0018 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| NA18954 | hp2 | a0001 | c0001 | t0005 | g0067 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| NA18957 | hp1 | a0001 | c0003 | t0007 | g0075 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| NA18957 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| NA18960 | hp1 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| NA18961 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| NA18962 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| NA18963 | hp1 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| NA18964 | hp2 | a0001 | c0003 | t0007 | g0008 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| NA18965 | hp1 | a0001 | c0001 | t0017 | g0050 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| NA18965 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0134 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| NA18971 | hp1 | a0001 | c0001 | t0008 | g0014 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0163 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| NA18972 | hp1 | a0001 | c0001 | t0008 | g0139 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| NA18972 | hp2 | a0001 | c0002 | t0001 | g0026 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| NA18973 | hp1 | a0001 | c0004 | t0002 | g0010 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| NA18973 | hp2 | a0001 | c0001 | t0018 | g0051 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| NA18974 | hp1 | a0001 | c0002 | t0001 | g0090 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| NA18974 | hp2 | a0001 | c0001 | t0013 | g0049 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| NA18978 | hp1 | a0001 | c0004 | t0002 | g0010 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| NA18978 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| NA18979 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| NA18980 | hp1 | a0001 | c0002 | t0020 | g0053 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| NA18985 | hp1 | a0001 | c0001 | t0002 | g0150 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| NA18985 | hp2 | a0001 | c0001 | t0006 | g0012 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| NA18987 | hp1 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| NA18987 | hp2 | a0001 | c0001 | t0006 | g0095 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| NA18990 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| NA18990 | hp2 | a0001 | c0004 | t0002 | g0010 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| NA18991 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| NA18991 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| NA18993 | hp2 | a0001 | c0002 | t0001 | g0037 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0145 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| NA18994 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| NA18997 | hp1 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| NA18997 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| NA18998 | hp1 | a0001 | c0003 | t0007 | g0008 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| NA18999 | hp1 | a0001 | c0004 | t0002 | g0010 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0138 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| NA19001 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| NA19001 | hp2 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| NA19003 | hp1 | a0001 | c0002 | t0001 | g0026 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| NA19005 | hp1 | a0001 | c0001 | t0008 | g0014 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| NA19005 | hp2 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| NA19006 | hp1 | a0001 | c0002 | t0001 | g0037 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| NA19006 | hp2 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| NA19009 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| NA19009 | hp2 | a0001 | c0002 | t0001 | g0097 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| NA19030 | hp1 | a0001 | c0001 | t0003 | g0023 | AFR | LWK | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| NA19030 | hp2 | a0001 | c0002 | t0001 | g0094 | AFR | LWK | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| NA19043 | hp1 | a0001 | c0011 | t0006 | g0076 | AFR | LWK | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| NA19043 | hp2 | a0001 | c0001 | t0005 | g0061 | AFR | LWK | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0161 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| NA19057 | hp2 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| NA19060 | hp1 | a0001 | c0003 | t0007 | g0078 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| NA19060 | hp2 | a0001 | c0004 | t0002 | g0151 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| NA19062 | hp1 | a0001 | c0002 | t0001 | g0084 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| NA19062 | hp2 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| NA19063 | hp1 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| NA19065 | hp1 | a0001 | c0004 | t0002 | g0136 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| NA19065 | hp2 | a0001 | c0006 | t0002 | g0013 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| NA19067 | hp1 | a0001 | c0001 | t0002 | g0122 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| NA19067 | hp2 | a0001 | c0001 | t0006 | g0012 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| NA19068 | hp1 | a0001 | c0004 | t0025 | g0165 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| NA19068 | hp2 | a0001 | c0001 | t0011 | g0046 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| NA19078 | hp1 | a0001 | c0001 | t0013 | g0049 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| NA19078 | hp2 | a0001 | c0001 | t0011 | g0046 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| NA19079 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| NA19079 | hp2 | a0001 | c0001 | t0008 | g0156 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| NA19084 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| NA19084 | hp2 | a0001 | c0003 | t0007 | g0008 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| NA19085 | hp1 | a0001 | c0002 | t0001 | g0121 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0141 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| NA19086 | hp2 | a0001 | c0007 | t0003 | g0018 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| NA19088 | hp1 | a0001 | c0004 | t0002 | g0010 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| NA19088 | hp2 | a0001 | c0002 | t0001 | g0088 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| NA19091 | hp1 | a0001 | c0001 | t0005 | g0022 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| NA19091 | hp2 | a0001 | c0002 | t0001 | g0026 | EAS | JPT | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| NA19240 | hp1 | a0001 | c0001 | t0016 | g0034 | AFR | YRI | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| NA19240 | hp2 | a0001 | c0001 | t0005 | g0064 | AFR | YRI | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| NA20129 | hp1 | a0001 | c0001 | t0006 | g0033 | AFR | ASW | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| NA20129 | hp2 | a0001 | c0001 | t0005 | g0065 | AFR | ASW | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| NA20752 | hp1 | a0001 | c0002 | t0001 | g0002 | EUR | TSI | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| NA20752 | hp2 | a0001 | c0002 | t0001 | g0006 | EUR | TSI | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| NA20805 | hp1 | a0001 | c0002 | t0001 | g0113 | EUR | TSI | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0030 | EUR | TSI | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| NA20905 | hp1 | a0001 | c0002 | t0001 | g0096 | SAS | GIH | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| NA20905 | hp2 | a0001 | c0002 | t0001 | g0027 | SAS | GIH | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG02109 | hp1 | a0001 | c0001 | t0016 | g0034 | AFR | ACB | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG02109 | hp2 | a0006 | c0015 | t0004 | g0117 | AFR | ACB | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG02486 | hp1 | a0001 | c0002 | t0001 | g0169 | AFR | ACB | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG02486 | hp2 | a0001 | c0001 | t0004 | g0004 | AFR | ACB | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG02559 | hp1 | a0004 | c0010 | t0005 | g0032 | AFR | ACB | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG02559 | hp2 | a0001 | c0001 | t0004 | g0004 | AFR | ACB | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG03471 | hp1 | a0001 | c0001 | t0005 | g0063 | AFR | MSL | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG03471 | hp2 | a0001 | c0001 | t0004 | g0004 | AFR | MSL | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG06807 | hp1 | a0001 | c0001 | t0004 | g0040 | AFR | USA | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| HG06807 | hp2 | a0001 | c0002 | t0001 | g0101 | AFR | USA | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| NA20300 | hp1 | a0001 | c0001 | t0005 | g0015 | AFR | USA | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| NA20300 | hp2 | a0001 | c0001 | t0004 | g0028 | AFR | USA | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| NA21309 | hp1 | a0001 | c0001 | t0006 | g0068 | AFR | LWK | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| NA21309 | hp2 | a0001 | c0001 | t0003 | g0071 | AFR | LWK | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0157 | REF | REF | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0001 | g0168 | REF | REF | CHST10_chr2_100386860_100422668 | CHST10 | chr2 | 100386860 | 100422668 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:100393298 | C | T | 1 | a0006 | 1 | HG02109.hp2 | missense_variant | MODERATE | c.1018G>A | p.Glu340Lys | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 7/7 | 1416/2854 | 1018/1071 | 340/356 | chr2 | 100393298 | |||
| chr2:100395526 | A | T | 1 | a0004 | 2 | HG02559.hp1 HG02647.hp2 |
missense_variant | MODERATE | c.516T>A | p.Asp172Glu | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 6/7 | 914/2854 | 516/1071 | 172/356 | chr2 | 100395526 | |||
| chr2:100395606 | A | G | 2 | a0002 a0007 |
10 | HG02257.hp1 HG02717.hp1 HG02896.hp1 others(7): Show |
missense_variant | MODERATE | c.436T>C | p.Ser146Pro | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 6/7 | 834/2854 | 436/1071 | 146/356 | chr2 | 100395606 | |||
| chr2:100402655 | A | G | 1 | a0007 | 1 | HG03540.hp2 | missense_variant&splice_region_variant | MODERATE | c.101T>C | p.Val34Ala | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 4/7 | 499/2854 | 101/1071 | 34/356 | chr2 | 100402655 | |||
| chr2:100406618 | C | A | 1 | a0003 | 5 | HG02280.hp1 HG02895.hp1 HG02965.hp1 others(2): Show |
missense_variant | MODERATE | c.58G>T | p.Val20Leu | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 3/7 | 456/2854 | 58/1071 | 20/356 | chr2 | 100406618 | |||
| chr2:100406648 | C | T | 1 | a0005 | 1 | HG01243.hp1 | missense_variant | MODERATE | c.28G>A | p.Ala10Thr | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 3/7 | 426/2854 | 28/1071 | 10/356 | chr2 | 100406648 | |||
| chr2:100417374 | C | G | 1 | a0002 | 3 | HG02257.hp1 HG02717.hp1 HG02922.hp2 |
splice_region_variant | LOW | c.-104G>C | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 1/7 | chr2 | 100417374 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:100393272 | G | A | 1 | a0001c0016 | 1 | HG02738.hp2 | synonymous_variant | LOW | c.1044C>T | p.Tyr348Tyr | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 7/7 | 1442/2854 | 1044/1071 | 348/356 | chr2 | 100393272 | |||
| chr2:100393386 | C | T | 1 | a0002c0005 | 7 | HG02257.hp1 HG02717.hp1 HG02896.hp2 others(4): Show |
synonymous_variant | LOW | c.930G>A | p.Pro310Pro | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 7/7 | 1328/2854 | 930/1071 | 310/356 | chr2 | 100393386 | |||
| chr2:100393446 | G | A | 1 | a0001c0003 | 11 | HG00423.hp1 HG00544.hp2 HG02056.hp1 others(8): Show |
synonymous_variant | LOW | c.870C>T | p.Ala290Ala | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 7/7 | 1268/2854 | 870/1071 | 290/356 | chr2 | 100393446 | |||
| chr2:100393557 | G | A | 1 | a0001c0007 | 5 | NA18939.hp1 NA18941.hp1 NA18945.hp2 others(2): Show |
synonymous_variant | LOW | c.759C>T | p.Asp253Asp | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 7/7 | 1157/2854 | 759/1071 | 253/356 | chr2 | 100393557 | |||
| chr2:100393575 | C | T | 1 | a0001c0014 | 1 | HG02809.hp2 | synonymous_variant | LOW | c.741G>A | p.Pro247Pro | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 7/7 | 1139/2854 | 741/1071 | 247/356 | chr2 | 100393575 | |||
| chr2:100393581 | G | A | 1 | a0001c0004 | 9 | HG00609.hp2 NA18973.hp1 NA18978.hp1 others(6): Show |
synonymous_variant | LOW | c.735C>T | p.Gly245Gly | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 7/7 | 1133/2854 | 735/1071 | 245/356 | chr2 | 100393581 | |||
| chr2:100393620 | G | C | 12 | a0001c0001 a0001c0003 a0001c0004 others(9): Show |
230 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(227): Show |
synonymous_variant | LOW | c.696C>G | p.Thr232Thr | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 7/7 | 1094/2854 | 696/1071 | 232/356 | chr2 | 100393620 | |||
| chr2:100395598 | A | G | 1 | a0001c0006 | 5 | HG00544.hp1 HG00621.hp2 HG02040.hp2 others(2): Show |
synonymous_variant | LOW | c.444T>C | p.Ile148Ile | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 6/7 | 842/2854 | 444/1071 | 148/356 | chr2 | 100395598 | |||
| chr2:100402569 | G | A | 2 | a0001c0003 a0001c0011 |
13 | HG00423.hp1 HG00544.hp2 HG02056.hp1 others(10): Show |
synonymous_variant | LOW | c.187C>T | p.Leu63Leu | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 4/7 | 585/2854 | 187/1071 | 63/356 | chr2 | 100402569 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:100392055 | T | C | 1 | a0002c0005t0022 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1190A>G | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 7/7 | 1190 | chr2 | 100392055 | ||||||
| chr2:100392104 | G | A | 9 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0023 others(6): Show |
72 | HG00423.hp1 HG00544.hp2 HG00735.hp1 others(69): Show |
3_prime_UTR_variant | MODIFIER | c.*1141C>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 7/7 | 1141 | chr2 | 100392104 | ||||||
| chr2:100392105 | C | A | 9 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0023 others(6): Show |
72 | HG00423.hp1 HG00544.hp2 HG00735.hp1 others(69): Show |
3_prime_UTR_variant | MODIFIER | c.*1140G>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 7/7 | 1140 | chr2 | 100392105 | ||||||
| chr2:100392393 | G | A | 1 | a0001c0002t0015 | 2 | HG00323.hp1 HG02698.hp2 |
3_prime_UTR_variant | MODIFIER | c.*852C>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 7/7 | 852 | chr2 | 100392393 | ||||||
| chr2:100392432 | C | T | 4 | a0002c0005t0009 a0002c0005t0010 a0002c0005t0022 others(1): Show |
7 | HG02257.hp1 HG02717.hp1 HG02896.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*813G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 7/7 | 813 | chr2 | 100392432 | ||||||
| chr2:100392487 | C | T | 1 | a0001c0003t0007 | 11 | HG00423.hp1 HG00544.hp2 HG02056.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*758G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 7/7 | 758 | chr2 | 100392487 | ||||||
| chr2:100392605 | T | C | 1 | a0001c0001t0019 | 1 | HG04184.hp2 | 3_prime_UTR_variant | MODIFIER | c.*640A>G | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 7/7 | 640 | chr2 | 100392605 | ||||||
| chr2:100392617 | G | A | 1 | a0002c0005t0009 | 3 | HG02896.hp2 HG03225.hp1 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*628C>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 7/7 | 628 | chr2 | 100392617 | ||||||
| chr2:100392620 | C | T | 11 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0018 others(8): Show |
74 | HG00423.hp1 HG00544.hp2 HG00735.hp1 others(71): Show |
3_prime_UTR_variant | MODIFIER | c.*625G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 7/7 | 625 | chr2 | 100392620 | ||||||
| chr2:100392709 | C | T | 1 | a0001c0002t0026 | 1 | HG01081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*536G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 7/7 | 536 | chr2 | 100392709 | ||||||
| chr2:100392710 | G | A | 1 | a0001c0001t0024 | 1 | HG00438.hp2 | 3_prime_UTR_variant | MODIFIER | c.*535C>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 7/7 | 535 | chr2 | 100392710 | ||||||
| chr2:100392776 | C | T | 11 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0018 others(8): Show |
74 | HG00423.hp1 HG00544.hp2 HG00735.hp1 others(71): Show |
3_prime_UTR_variant | MODIFIER | c.*469G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 7/7 | 469 | chr2 | 100392776 | ||||||
| chr2:100392860 | A | G | 1 | a0001c0001t0012 | 2 | HG01192.hp2 HG01261.hp1 |
3_prime_UTR_variant | MODIFIER | c.*385T>C | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 7/7 | 385 | chr2 | 100392860 | ||||||
| chr2:100392864 | T | C | 30 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(27): Show |
231 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(228): Show |
3_prime_UTR_variant | MODIFIER | c.*381A>G | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 7/7 | 381 | chr2 | 100392864 | ||||||
| chr2:100392894 | C | A | 1 | a0001c0001t0029 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*351G>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 7/7 | 351 | chr2 | 100392894 | ||||||
| chr2:100392923 | C | T | 5 | a0001c0001t0003 a0001c0001t0023 a0001c0007t0003 others(2): Show |
40 | HG00735.hp1 HG00741.hp2 HG01243.hp1 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*322G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 7/7 | 322 | chr2 | 100392923 | ||||||
| chr2:100392927 | C | T | 1 | a0001c0002t0014 | 2 | HG03490.hp1 HG03492.hp1 |
3_prime_UTR_variant | MODIFIER | c.*318G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 7/7 | 318 | chr2 | 100392927 | ||||||
| chr2:100393025 | C | T | 3 | a0001c0001t0004 a0001c0014t0004 a0006c0015t0004 |
23 | HG01516.hp1 HG02055.hp1 HG02109.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*220G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 7/7 | 220 | chr2 | 100393025 | ||||||
| chr2:100393026 | G | T | 3 | a0001c0001t0004 a0001c0014t0004 a0006c0015t0004 |
23 | HG01516.hp1 HG02055.hp1 HG02109.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*219C>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 7/7 | 219 | chr2 | 100393026 | ||||||
| chr2:100393050 | G | T | 1 | a0001c0001t0011 | 2 | NA19068.hp2 NA19078.hp2 |
3_prime_UTR_variant | MODIFIER | c.*195C>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 7/7 | 195 | chr2 | 100393050 | ||||||
| chr2:100393104 | G | A | 2 | a0001c0001t0016 a0001c0001t0029 |
3 | HG01891.hp2 HG02109.hp1 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*141C>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 7/7 | 141 | chr2 | 100393104 | ||||||
| chr2:100393133 | C | T | 3 | a0001c0001t0004 a0001c0014t0004 a0006c0015t0004 |
23 | HG01516.hp1 HG02055.hp1 HG02109.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*112G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 7/7 | 112 | chr2 | 100393133 | ||||||
| chr2:100393138 | G | A | 15 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0008 others(12): Show |
133 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(130): Show |
3_prime_UTR_variant | MODIFIER | c.*107C>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 7/7 | 107 | chr2 | 100393138 | ||||||
| chr2:100393206 | A | G | 1 | a0001c0001t0008 | 9 | HG02083.hp1 HG02129.hp2 HG02155.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*39T>C | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 7/7 | 39 | chr2 | 100393206 | ||||||
| chr2:100415050 | C | A | 1 | a0001c0001t0013 | 2 | NA18974.hp2 NA19078.hp1 |
5_prime_UTR_variant | MODIFIER | c.-42G>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/7 | 8375 | chr2 | 100415050 | ||||||
| chr2:100415056 | G | A | 1 | a0001c0004t0025 | 1 | NA19068.hp1 | 5_prime_UTR_variant | MODIFIER | c.-48C>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/7 | 8381 | chr2 | 100415056 | ||||||
| chr2:100415099 | G | T | 12 | a0001c0001t0002 a0001c0001t0008 a0001c0001t0011 others(9): Show |
118 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(115): Show |
5_prime_UTR_variant | MODIFIER | c.-91C>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/7 | 8424 | chr2 | 100415099 | ||||||
| chr2:100417421 | C | T | 1 | a0001c0002t0021 | 1 | HG01358.hp2 | 5_prime_UTR_variant | MODIFIER | c.-151G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 1/7 | 10746 | chr2 | 100417421 | ||||||
| chr2:100417475 | G | T | 1 | a0001c0002t0020 | 1 | NA18980.hp1 | 5_prime_UTR_variant | MODIFIER | c.-205C>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 1/7 | 10800 | chr2 | 100417475 | ||||||
| chr2:100417532 | C | T | 2 | a0001c0001t0018 a0001c0001t0019 |
2 | HG04184.hp2 NA18973.hp2 |
5_prime_UTR_variant | MODIFIER | c.-262G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 1/7 | 10857 | chr2 | 100417532 | ||||||
| chr2:100417595 | C | T | 1 | a0001c0001t0017 | 1 | NA18965.hp1 | 5_prime_UTR_variant | MODIFIER | c.-325G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 1/7 | 10920 | chr2 | 100417595 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:100393897 | C | T | 7 | a0001c0001t0002g0009 a0001c0001t0002g0124 a0001c0001t0002g0125 others(4): Show |
13 | HG00639.hp2 HG01167.hp1 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.534-115G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 6/6 | chr2 | 100393897 | |||||||
| chr2:100393942 | A | G | 2 | a0002c0005t0009g0031 a0002c0005t0009g0059 |
3 | HG02896.hp2 HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.534-160T>C | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 6/6 | chr2 | 100393942 | |||||||
| chr2:100394208 | A | G | 3 | a0001c0001t0002g0132 a0001c0001t0002g0146 a0001c0001t0002g0153 |
3 | HG01515.hp1 HG02602.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.534-426T>C | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 6/6 | chr2 | 100394208 | |||||||
| chr2:100394251 | CAG | C | 29 | a0001c0001t0003g0005 a0001c0001t0003g0007 a0001c0001t0003g0023 others(26): Show |
67 | HG00735.hp1 HG00741.hp2 HG01167.hp2 others(64): Show |
intron_variant | MODIFIER | c.534-471_534-470del others(2): Show |
CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 6/6 | chr2 | 100394251 | |||||||
| chr2:100394266 | C | T | 3 | a0001c0001t0005g0062 a0001c0001t0005g0063 a0001c0001t0005g0065 |
3 | HG02258.hp1 HG03471.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.534-484G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 6/6 | chr2 | 100394266 | |||||||
| chr2:100394268 | C | T | 8 | a0001c0001t0004g0004 a0001c0001t0004g0028 a0001c0001t0004g0040 others(5): Show |
23 | HG01516.hp1 HG02055.hp1 HG02109.hp2 others(20): Show |
intron_variant | MODIFIER | c.534-486G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 6/6 | chr2 | 100394268 | |||||||
| chr2:100394306 | G | A | 1 | a0001c0002t0001g0037 | 2 | NA18993.hp2 NA19006.hp1 |
intron_variant | MODIFIER | c.534-524C>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 6/6 | chr2 | 100394306 | |||||||
| chr2:100394398 | G | A | 67 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0021 others(64): Show |
132 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.534-616C>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 6/6 | chr2 | 100394398 | |||||||
| chr2:100394405 | C | A | 67 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0021 others(64): Show |
132 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.534-623G>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 6/6 | chr2 | 100394405 | |||||||
| chr2:100394406 | G | A | 7 | a0001c0002t0001g0116 a0002c0005t0009g0031 a0002c0005t0009g0059 others(4): Show |
9 | HG02257.hp1 HG02572.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.534-624C>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 6/6 | chr2 | 100394406 | |||||||
| chr2:100394479 | T | G | 3 | a0001c0001t0005g0015 a0001c0001t0005g0064 a0004c0010t0005g0032 |
7 | HG01261.hp2 HG02055.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.534-697A>C | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 6/6 | chr2 | 100394479 | |||||||
| chr2:100394560 | C | T | 1 | a0001c0001t0003g0007 | 9 | HG00735.hp1 HG00741.hp2 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.534-778G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 6/6 | chr2 | 100394560 | |||||||
| chr2:100394624 | C | T | 1 | a0002c0005t0027g0058 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.534-842G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 6/6 | chr2 | 100394624 | |||||||
| chr2:100394726 | C | CT | 30 | a0001c0001t0003g0005 a0001c0001t0003g0007 a0001c0001t0003g0023 others(27): Show |
68 | HG00735.hp1 HG00741.hp2 HG01167.hp2 others(65): Show |
intron_variant | MODIFIER | c.533+782dupA | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 6/6 | chr2 | 100394726 | |||||||
| chr2:100394726 | CT | C | 62 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0021 others(59): Show |
125 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.533+782delA | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 6/6 | chr2 | 100394726 | |||||||
| chr2:100394746 | C | T | 2 | a0001c0002t0001g0025 a0001c0002t0001g0083 |
4 | HG01168.hp2 HG01169.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.533+763G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 6/6 | chr2 | 100394746 | |||||||
| chr2:100394779 | G | A | 115 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0021 others(112): Show |
244 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(241): Show |
intron_variant | MODIFIER | c.533+730C>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 6/6 | chr2 | 100394779 | |||||||
| chr2:100394790 | C | G | 33 | a0001c0001t0003g0005 a0001c0001t0003g0007 a0001c0001t0003g0023 others(30): Show |
79 | HG00423.hp1 HG00544.hp2 HG00735.hp1 others(76): Show |
intron_variant | MODIFIER | c.533+719G>C | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 6/6 | chr2 | 100394790 | |||||||
| chr2:100394819 | G | T | 1 | a0001c0002t0001g0108 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.533+690C>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 6/6 | chr2 | 100394819 | |||||||
| chr2:100394889 | AT | A | 66 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0021 others(63): Show |
131 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(128): Show |
intron_variant | MODIFIER | c.533+619delA | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 6/6 | chr2 | 100394889 | |||||||
| chr2:100395062 | C | T | 1 | a0007c0013t0028g0077 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.533+447G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 6/6 | chr2 | 100395062 | |||||||
| chr2:100395087 | C | T | 2 | a0001c0001t0005g0022 a0001c0001t0005g0067 |
4 | HG02148.hp2 NA18953.hp2 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.533+422G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 6/6 | chr2 | 100395087 | |||||||
| chr2:100395156 | A | G | 37 | a0001c0001t0003g0005 a0001c0001t0003g0007 a0001c0001t0003g0023 others(34): Show |
84 | HG00423.hp1 HG00544.hp2 HG00735.hp1 others(81): Show |
intron_variant | MODIFIER | c.533+353T>C | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 6/6 | chr2 | 100395156 | |||||||
| chr2:100395262 | C | T | 115 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0021 others(112): Show |
244 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(241): Show |
intron_variant | MODIFIER | c.533+247G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 6/6 | chr2 | 100395262 | |||||||
| chr2:100395415 | T | C | 67 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0021 others(64): Show |
132 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.533+94A>G | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 6/6 | chr2 | 100395415 | |||||||
| chr2:100395478 | C | A | 1 | a0001c0001t0003g0071 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.533+31G>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 6/6 | chr2 | 100395478 | |||||||
| chr2:100395487 | C | A | 4 | a0001c0001t0003g0023 a0001c0001t0003g0071 a0001c0001t0003g0073 others(1): Show |
6 | HG01243.hp1 HG02647.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.533+22G>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 6/6 | chr2 | 100395487 | |||||||
| chr2:100395658 | C | T | 1 | a0001c0001t0002g0145 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.428-44G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 5/6 | chr2 | 100395658 | |||||||
| chr2:100395717 | C | T | 2 | a0001c0001t0018g0051 a0001c0001t0019g0052 |
2 | HG04184.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.428-103G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 5/6 | chr2 | 100395717 | |||||||
| chr2:100395740 | C | T | 1 | a0001c0002t0001g0101 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.428-126G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 5/6 | chr2 | 100395740 | |||||||
| chr2:100395839 | C | T | 2 | a0001c0001t0005g0022 a0001c0001t0005g0067 |
4 | HG02148.hp2 NA18953.hp2 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.428-225G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 5/6 | chr2 | 100395839 | |||||||
| chr2:100395865 | G | A | 2 | a0001c0001t0018g0051 a0001c0001t0019g0052 |
2 | HG04184.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.428-251C>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 5/6 | chr2 | 100395865 | |||||||
| chr2:100396051 | C | T | 6 | a0001c0002t0021g0054 a0002c0005t0009g0031 a0002c0005t0009g0059 others(3): Show |
7 | HG01358.hp2 HG02257.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.428-437G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 5/6 | chr2 | 100396051 | |||||||
| chr2:100396077 | T | C | 1 | a0007c0013t0028g0077 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.428-463A>G | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 5/6 | chr2 | 100396077 | |||||||
| chr2:100396246 | G | GT | 6 | a0002c0005t0009g0031 a0002c0005t0009g0059 a0002c0005t0010g0055 others(3): Show |
7 | HG02257.hp1 HG02717.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.428-633dupA | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 5/6 | chr2 | 100396246 | |||||||
| chr2:100396324 | A | C | 1 | a0001c0002t0001g0098 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.428-710T>G | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 5/6 | chr2 | 100396324 | |||||||
| chr2:100396332 | C | G | 1 | a0001c0001t0002g0144 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.428-718G>C | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 5/6 | chr2 | 100396332 | |||||||
| chr2:100396406 | G | C | 1 | a0001c0001t0002g0150 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.428-792C>G | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 5/6 | chr2 | 100396406 | |||||||
| chr2:100396471 | T | A | 1 | a0001c0011t0006g0076 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.428-857A>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 5/6 | chr2 | 100396471 | |||||||
| chr2:100396595 | T | A | 2 | a0001c0002t0001g0020 a0001c0002t0001g0100 |
5 | HG02300.hp2 HG02572.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.428-981A>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 5/6 | chr2 | 100396595 | |||||||
| chr2:100396622 | G | A | 3 | a0001c0002t0001g0006 a0001c0002t0001g0087 a0001c0002t0001g0103 |
12 | HG00140.hp1 HG00280.hp1 HG00639.hp1 others(9): Show |
intron_variant | MODIFIER | c.428-1008C>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 5/6 | chr2 | 100396622 | |||||||
| chr2:100396631 | G | A | 1 | a0001c0002t0001g0170 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.428-1017C>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 5/6 | chr2 | 100396631 | |||||||
| chr2:100396924 | A | G | 3 | a0001c0001t0008g0123 a0001c0001t0008g0143 a0001c0001t0008g0156 |
3 | HG02155.hp1 NA18612.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.427+984T>C | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 5/6 | chr2 | 100396924 | |||||||
| chr2:100396958 | T | A | 3 | a0001c0001t0005g0015 a0001c0001t0005g0064 a0004c0010t0005g0032 |
7 | HG01261.hp2 HG02055.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.427+950A>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 5/6 | chr2 | 100396958 | |||||||
| chr2:100396962 | T | C | 2 | a0001c0002t0001g0025 a0001c0002t0001g0083 |
4 | HG01168.hp2 HG01169.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.427+946A>G | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 5/6 | chr2 | 100396962 | |||||||
| chr2:100396970 | C | G | 1 | a0007c0013t0028g0077 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.427+938G>C | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 5/6 | chr2 | 100396970 | |||||||
| chr2:100397041 | C | T | 3 | a0001c0001t0002g0021 a0001c0001t0002g0043 a0001c0001t0002g0122 |
7 | HG00597.hp1 NA18945.hp1 NA18963.hp2 others(4): Show |
intron_variant | MODIFIER | c.427+867G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 5/6 | chr2 | 100397041 | |||||||
| chr2:100397187 | A | G | 67 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0021 others(64): Show |
132 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.427+721T>C | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 5/6 | chr2 | 100397187 | |||||||
| chr2:100397198 | C | T | 3 | a0001c0001t0005g0015 a0001c0001t0005g0064 a0004c0010t0005g0032 |
7 | HG01261.hp2 HG02055.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.427+710G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 5/6 | chr2 | 100397198 | |||||||
| chr2:100397213 | T | C | 2 | a0001c0001t0018g0051 a0001c0001t0019g0052 |
2 | HG04184.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.427+695A>G | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 5/6 | chr2 | 100397213 | |||||||
| chr2:100397280 | G | T | 1 | a0007c0013t0028g0077 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.427+628C>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 5/6 | chr2 | 100397280 | |||||||
| chr2:100397433 | C | T | 2 | a0001c0001t0006g0033 a0001c0001t0006g0080 |
3 | HG02257.hp2 HG03130.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.427+475G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 5/6 | chr2 | 100397433 | |||||||
| chr2:100397540 | C | T | 1 | a0001c0001t0004g0119 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.427+368G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 5/6 | chr2 | 100397540 | |||||||
| chr2:100397582 | T | C | 2 | a0001c0002t0001g0110 a0002c0009t0001g0042 |
3 | HG02896.hp1 HG02897.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.427+326A>G | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 5/6 | chr2 | 100397582 | |||||||
| chr2:100397734 | A | C | 2 | a0002c0005t0009g0031 a0002c0005t0009g0059 |
3 | HG02896.hp2 HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.427+174T>G | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 5/6 | chr2 | 100397734 | |||||||
| chr2:100397759 | A | G | 6 | a0002c0005t0009g0031 a0002c0005t0009g0059 a0002c0005t0010g0055 others(3): Show |
7 | HG02257.hp1 HG02717.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.427+149T>C | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 5/6 | chr2 | 100397759 | |||||||
| chr2:100397785 | C | A | 114 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0021 others(111): Show |
242 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(239): Show |
intron_variant | MODIFIER | c.427+123G>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 5/6 | chr2 | 100397785 | |||||||
| chr2:100397829 | T | A | 1 | a0001c0002t0001g0105 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.427+79A>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 5/6 | chr2 | 100397829 | |||||||
| chr2:100397901 | C | T | 59 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0021 others(56): Show |
121 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(118): Show |
splice_region_variant&intron_variant | LOW | c.427+7G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 5/6 | chr2 | 100397901 | |||||||
| chr2:100398162 | G | A | 2 | a0001c0002t0001g0019 a0001c0002t0001g0091 |
5 | HG00642.hp1 HG01496.hp1 HG01928.hp1 others(2): Show |
intron_variant | MODIFIER | c.193-20C>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 4/6 | chr2 | 100398162 | |||||||
| chr2:100398276 | T | C | 1 | a0001c0002t0001g0100 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.193-134A>G | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 4/6 | chr2 | 100398276 | |||||||
| chr2:100398339 | G | A | 3 | a0001c0003t0007g0008 a0001c0003t0007g0075 a0001c0003t0007g0078 |
11 | HG00423.hp1 HG00544.hp2 HG02056.hp1 others(8): Show |
intron_variant | MODIFIER | c.193-197C>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 4/6 | chr2 | 100398339 | |||||||
| chr2:100398342 | C | T | 2 | a0001c0001t0018g0051 a0001c0001t0019g0052 |
2 | HG04184.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.193-200G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 4/6 | chr2 | 100398342 | |||||||
| chr2:100398386 | A | ATG | 38 | a0001c0001t0003g0005 a0001c0001t0003g0007 a0001c0001t0003g0023 others(35): Show |
85 | HG00423.hp1 HG00544.hp2 HG00735.hp1 others(82): Show |
intron_variant | MODIFIER | c.193-245_193-244ins others(2): Show |
CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 4/6 | chr2 | 100398386 | |||||||
| chr2:100398548 | A | G | 1 | a0001c0002t0001g0107 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.193-406T>C | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 4/6 | chr2 | 100398548 | |||||||
| chr2:100398594 | C | T | 6 | a0002c0005t0009g0031 a0002c0005t0009g0059 a0002c0005t0010g0055 others(3): Show |
7 | HG02257.hp1 HG02717.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.193-452G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 4/6 | chr2 | 100398594 | |||||||
| chr2:100398607 | G | A | 6 | a0002c0005t0009g0031 a0002c0005t0009g0059 a0002c0005t0010g0055 others(3): Show |
7 | HG02257.hp1 HG02717.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.193-465C>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 4/6 | chr2 | 100398607 | |||||||
| chr2:100398664 | T | C | 2 | a0002c0009t0001g0042 a0007c0013t0028g0077 |
3 | HG02896.hp1 HG02897.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.193-522A>G | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 4/6 | chr2 | 100398664 | |||||||
| chr2:100398688 | G | C | 4 | a0001c0002t0001g0020 a0001c0002t0001g0099 a0001c0002t0001g0100 others(1): Show |
7 | HG01884.hp2 HG02300.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.193-546C>G | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 4/6 | chr2 | 100398688 | |||||||
| chr2:100398935 | C | T | 1 | a0001c0001t0002g0142 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.193-793G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 4/6 | chr2 | 100398935 | |||||||
| chr2:100398955 | G | A | 2 | a0001c0002t0001g0025 a0001c0002t0001g0083 |
4 | HG01168.hp2 HG01169.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.193-813C>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 4/6 | chr2 | 100398955 | |||||||
| chr2:100399102 | CT | C | 72 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0021 others(69): Show |
154 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(151): Show |
intron_variant | MODIFIER | c.193-961delA | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 4/6 | chr2 | 100399102 | |||||||
| chr2:100399102 | CTT | C | 6 | a0001c0001t0002g0137 a0001c0001t0002g0152 a0001c0001t0006g0095 others(3): Show |
6 | HG01257.hp2 HG01515.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.193-962_193-961del others(2): Show |
CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 4/6 | chr2 | 100399102 | |||||||
| chr2:100399103 | T | TC | 3 | a0001c0003t0007g0008 a0001c0003t0007g0075 a0001c0003t0007g0078 |
11 | HG00423.hp1 HG00544.hp2 HG02056.hp1 others(8): Show |
intron_variant | MODIFIER | c.193-962_193-961ins others(1): Show |
CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 4/6 | chr2 | 100399103 | |||||||
| chr2:100399106 | T | C | 2 | a0001c0001t0018g0051 a0001c0001t0019g0052 |
2 | HG04184.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.193-964A>G | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 4/6 | chr2 | 100399106 | |||||||
| chr2:100399113 | T | G | 23 | a0001c0001t0003g0005 a0001c0001t0003g0007 a0001c0001t0003g0023 others(20): Show |
60 | HG00735.hp1 HG00741.hp2 HG01167.hp2 others(57): Show |
intron_variant | MODIFIER | c.193-971A>C | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 4/6 | chr2 | 100399113 | |||||||
| chr2:100399139 | T | C | 67 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0021 others(64): Show |
132 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.193-997A>G | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 4/6 | chr2 | 100399139 | |||||||
| chr2:100399166 | C | A | 2 | a0001c0002t0001g0025 a0001c0002t0001g0083 |
4 | HG01168.hp2 HG01169.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.193-1024G>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 4/6 | chr2 | 100399166 | |||||||
| chr2:100399398 | C | T | 3 | a0001c0003t0007g0008 a0001c0003t0007g0075 a0001c0003t0007g0078 |
11 | HG00423.hp1 HG00544.hp2 HG02056.hp1 others(8): Show |
intron_variant | MODIFIER | c.193-1256G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 4/6 | chr2 | 100399398 | |||||||
| chr2:100399580 | G | A | 5 | a0001c0001t0018g0051 a0001c0001t0019g0052 a0001c0003t0007g0008 others(2): Show |
13 | HG00423.hp1 HG00544.hp2 HG02056.hp1 others(10): Show |
intron_variant | MODIFIER | c.193-1438C>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 4/6 | chr2 | 100399580 | |||||||
| chr2:100399591 | A | G | 1 | a0001c0002t0001g0083 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.193-1449T>C | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 4/6 | chr2 | 100399591 | |||||||
| chr2:100399846 | C | T | 1 | a0001c0002t0001g0060 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.193-1704G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 4/6 | chr2 | 100399846 | |||||||
| chr2:100399948 | C | T | 1 | a0001c0002t0001g0097 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.193-1806G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 4/6 | chr2 | 100399948 | |||||||
| chr2:100399979 | G | A | 1 | a0001c0001t0002g0130 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.193-1837C>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 4/6 | chr2 | 100399979 | |||||||
| chr2:100400093 | G | A | 1 | a0007c0013t0028g0077 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.193-1951C>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 4/6 | chr2 | 100400093 | |||||||
| chr2:100400208 | A | G | 1 | a0001c0001t0002g0140 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.193-2066T>C | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 4/6 | chr2 | 100400208 | |||||||
| chr2:100400214 | C | T | 1 | a0001c0002t0001g0096 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.193-2072G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 4/6 | chr2 | 100400214 | |||||||
| chr2:100400267 | TCTTGTTC others(5): Show |
T | 1 | a0001c0001t0002g0130 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.193-2137_193-2126d others(14): Show |
CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 4/6 | chr2 | 100400267 | |||||||
| chr2:100400438 | G | C | 2 | a0001c0001t0018g0051 a0001c0001t0019g0052 |
2 | HG04184.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.192+2126C>G | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 4/6 | chr2 | 100400438 | |||||||
| chr2:100400569 | T | C | 1 | a0001c0001t0017g0050 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.192+1995A>G | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 4/6 | chr2 | 100400569 | |||||||
| chr2:100400673 | T | C | 1 | a0001c0002t0001g0101 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.192+1891A>G | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 4/6 | chr2 | 100400673 | |||||||
| chr2:100400803 | C | T | 3 | a0001c0001t0002g0029 a0001c0001t0002g0133 a0001c0001t0011g0046 |
6 | HG00423.hp2 HG02155.hp2 NA18968.hp2 others(3): Show |
intron_variant | MODIFIER | c.192+1761G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 4/6 | chr2 | 100400803 | |||||||
| chr2:100400883 | G | A | 8 | a0001c0001t0004g0004 a0001c0001t0004g0028 a0001c0001t0004g0040 others(5): Show |
23 | HG01516.hp1 HG02055.hp1 HG02109.hp2 others(20): Show |
intron_variant | MODIFIER | c.192+1681C>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 4/6 | chr2 | 100400883 | |||||||
| chr2:100400909 | G | C | 4 | a0001c0002t0001g0104 a0001c0002t0001g0111 a0001c0002t0001g0113 others(1): Show |
5 | HG00738.hp2 HG02683.hp2 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.192+1655C>G | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 4/6 | chr2 | 100400909 | |||||||
| chr2:100400974 | C | T | 1 | a0002c0009t0001g0042 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.192+1590G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 4/6 | chr2 | 100400974 | |||||||
| chr2:100401081 | T | C | 5 | a0001c0003t0007g0008 a0001c0003t0007g0075 a0001c0003t0007g0078 others(2): Show |
13 | HG00423.hp1 HG00544.hp2 HG02056.hp1 others(10): Show |
intron_variant | MODIFIER | c.192+1483A>G | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 4/6 | chr2 | 100401081 | |||||||
| chr2:100401296 | C | T | 35 | a0001c0001t0002g0045 a0001c0001t0003g0005 a0001c0001t0003g0007 others(32): Show |
82 | HG00423.hp1 HG00544.hp2 HG00735.hp1 others(79): Show |
intron_variant | MODIFIER | c.192+1268G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 4/6 | chr2 | 100401296 | |||||||
| chr2:100401434 | C | T | 2 | a0001c0001t0018g0051 a0001c0001t0019g0052 |
2 | HG04184.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.192+1130G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 4/6 | chr2 | 100401434 | |||||||
| chr2:100401435 | G | A | 3 | a0001c0001t0005g0015 a0001c0001t0005g0064 a0004c0010t0005g0032 |
7 | HG01261.hp2 HG02055.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.192+1129C>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 4/6 | chr2 | 100401435 | |||||||
| chr2:100401448 | C | T | 3 | a0001c0001t0005g0016 a0001c0001t0005g0061 a0001c0001t0005g0066 |
6 | HG01167.hp2 HG02622.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.192+1116G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 4/6 | chr2 | 100401448 | |||||||
| chr2:100401668 | A | G | 4 | a0001c0002t0001g0025 a0001c0002t0001g0083 a0002c0009t0001g0042 others(1): Show |
7 | HG01168.hp2 HG01169.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.192+896T>C | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 4/6 | chr2 | 100401668 | |||||||
| chr2:100401677 | A | C | 1 | a0002c0009t0001g0042 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.192+887T>G | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 4/6 | chr2 | 100401677 | |||||||
| chr2:100401719 | A | G | 1 | a0001c0002t0001g0106 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.192+845T>C | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 4/6 | chr2 | 100401719 | |||||||
| chr2:100401751 | C | A | 1 | a0001c0001t0002g0152 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.192+813G>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 4/6 | chr2 | 100401751 | |||||||
| chr2:100401754 | T | A | 2 | a0001c0001t0018g0051 a0001c0001t0019g0052 |
2 | HG04184.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.192+810A>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 4/6 | chr2 | 100401754 | |||||||
| chr2:100401881 | C | T | 8 | a0001c0001t0004g0004 a0001c0001t0004g0028 a0001c0001t0004g0040 others(5): Show |
23 | HG01516.hp1 HG02055.hp1 HG02109.hp2 others(20): Show |
intron_variant | MODIFIER | c.192+683G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 4/6 | chr2 | 100401881 | |||||||
| chr2:100401882 | G | A | 1 | a0002c0009t0001g0042 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.192+682C>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 4/6 | chr2 | 100401882 | |||||||
| chr2:100401949 | C | G | 40 | a0001c0001t0003g0005 a0001c0001t0003g0007 a0001c0001t0003g0023 others(37): Show |
89 | HG00423.hp1 HG00544.hp2 HG00735.hp1 others(86): Show |
intron_variant | MODIFIER | c.192+615G>C | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 4/6 | chr2 | 100401949 | |||||||
| chr2:100401983 | C | T | 34 | a0001c0001t0003g0005 a0001c0001t0003g0007 a0001c0001t0003g0023 others(31): Show |
80 | HG00423.hp1 HG00544.hp2 HG00735.hp1 others(77): Show |
intron_variant | MODIFIER | c.192+581G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 4/6 | chr2 | 100401983 | |||||||
| chr2:100402160 | A | G | 8 | a0001c0001t0004g0004 a0001c0001t0004g0028 a0001c0001t0004g0040 others(5): Show |
23 | HG01516.hp1 HG02055.hp1 HG02109.hp2 others(20): Show |
intron_variant | MODIFIER | c.192+404T>C | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 4/6 | chr2 | 100402160 | |||||||
| chr2:100402251 | T | A | 1 | a0001c0001t0003g0024 | 3 | HG03491.hp2 HG03492.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.192+313A>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 4/6 | chr2 | 100402251 | |||||||
| chr2:100402460 | C | T | 1 | a0001c0001t0006g0079 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.192+104G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 4/6 | chr2 | 100402460 | |||||||
| chr2:100402466 | C | T | 1 | a0001c0001t0008g0139 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.192+98G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 4/6 | chr2 | 100402466 | |||||||
| chr2:100402756 | C | T | 2 | a0001c0001t0018g0051 a0001c0001t0019g0052 |
2 | HG04184.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.101-101G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 3/6 | chr2 | 100402756 | |||||||
| chr2:100402762 | C | T | 1 | a0001c0002t0001g0035 | 2 | HG02809.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.101-107G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 3/6 | chr2 | 100402762 | |||||||
| chr2:100402775 | C | T | 2 | a0001c0002t0001g0025 a0001c0002t0001g0083 |
4 | HG01168.hp2 HG01169.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.101-120G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 3/6 | chr2 | 100402775 | |||||||
| chr2:100402941 | T | C | 2 | a0001c0001t0018g0051 a0001c0001t0019g0052 |
2 | HG04184.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.101-286A>G | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 3/6 | chr2 | 100402941 | |||||||
| chr2:100403201 | G | A | 128 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0021 others(125): Show |
276 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.101-546C>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 3/6 | chr2 | 100403201 | |||||||
| chr2:100403345 | C | T | 6 | a0001c0001t0005g0016 a0001c0001t0005g0061 a0001c0001t0005g0062 others(3): Show |
9 | HG01167.hp2 HG02258.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.101-690G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 3/6 | chr2 | 100403345 | |||||||
| chr2:100403347 | T | C | 1 | a0001c0001t0002g0153 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.101-692A>G | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 3/6 | chr2 | 100403347 | |||||||
| chr2:100403453 | C | T | 1 | a0001c0001t0005g0066 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.101-798G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 3/6 | chr2 | 100403453 | |||||||
| chr2:100403466 | T | C | 2 | a0001c0001t0018g0051 a0001c0001t0019g0052 |
2 | HG04184.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.101-811A>G | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 3/6 | chr2 | 100403466 | |||||||
| chr2:100403572 | G | A | 1 | a0001c0001t0002g0154 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.101-917C>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 3/6 | chr2 | 100403572 | |||||||
| chr2:100403618 | T | C | 6 | a0002c0005t0009g0031 a0002c0005t0009g0059 a0002c0005t0010g0055 others(3): Show |
7 | HG02257.hp1 HG02717.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.101-963A>G | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 3/6 | chr2 | 100403618 | |||||||
| chr2:100403674 | C | T | 1 | a0001c0001t0002g0138 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.101-1019G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 3/6 | chr2 | 100403674 | |||||||
| chr2:100403675 | G | A | 36 | a0001c0001t0003g0005 a0001c0001t0003g0007 a0001c0001t0003g0023 others(33): Show |
82 | HG00423.hp1 HG00544.hp2 HG00735.hp1 others(79): Show |
intron_variant | MODIFIER | c.101-1020C>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 3/6 | chr2 | 100403675 | |||||||
| chr2:100403775 | C | T | 5 | a0001c0001t0002g0009 a0001c0001t0002g0124 a0001c0001t0002g0125 others(2): Show |
11 | HG00639.hp2 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.101-1120G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 3/6 | chr2 | 100403775 | |||||||
| chr2:100403777 | A | G | 1 | a0007c0013t0028g0077 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.101-1122T>C | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 3/6 | chr2 | 100403777 | |||||||
| chr2:100403818 | T | G | 1 | a0007c0013t0028g0077 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.101-1163A>C | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 3/6 | chr2 | 100403818 | |||||||
| chr2:100403843 | G | A | 167 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0021 others(164): Show |
361 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(358): Show |
intron_variant | MODIFIER | c.101-1188C>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 3/6 | chr2 | 100403843 | |||||||
| chr2:100403970 | G | C | 4 | a0001c0002t0001g0025 a0001c0002t0001g0083 a0002c0009t0001g0042 others(1): Show |
7 | HG01168.hp2 HG01169.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.101-1315C>G | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 3/6 | chr2 | 100403970 | |||||||
| chr2:100404098 | G | C | 2 | a0001c0001t0016g0034 a0001c0001t0029g0082 |
3 | HG01891.hp2 HG02109.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.101-1443C>G | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 3/6 | chr2 | 100404098 | |||||||
| chr2:100404162 | G | A | 30 | a0001c0001t0003g0005 a0001c0001t0003g0007 a0001c0001t0003g0023 others(27): Show |
75 | HG00423.hp1 HG00544.hp2 HG00735.hp1 others(72): Show |
intron_variant | MODIFIER | c.101-1507C>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 3/6 | chr2 | 100404162 | |||||||
| chr2:100404168 | G | A | 2 | a0001c0001t0005g0022 a0001c0001t0005g0067 |
4 | HG02148.hp2 NA18953.hp2 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.101-1513C>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 3/6 | chr2 | 100404168 | |||||||
| chr2:100404256 | G | A | 2 | a0001c0001t0018g0051 a0001c0001t0019g0052 |
2 | HG04184.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.101-1601C>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 3/6 | chr2 | 100404256 | |||||||
| chr2:100404382 | C | T | 2 | a0001c0002t0001g0027 a0001c0002t0001g0105 |
4 | HG01099.hp1 HG01175.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.101-1727G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 3/6 | chr2 | 100404382 | |||||||
| chr2:100404436 | G | A | 34 | a0001c0001t0003g0005 a0001c0001t0003g0007 a0001c0001t0003g0023 others(31): Show |
80 | HG00423.hp1 HG00544.hp2 HG00735.hp1 others(77): Show |
intron_variant | MODIFIER | c.101-1781C>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 3/6 | chr2 | 100404436 | |||||||
| chr2:100404583 | T | C | 2 | a0001c0002t0001g0025 a0001c0002t0001g0083 |
4 | HG01168.hp2 HG01169.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.101-1928A>G | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 3/6 | chr2 | 100404583 | |||||||
| chr2:100404628 | A | G | 115 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0021 others(112): Show |
244 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(241): Show |
intron_variant | MODIFIER | c.100+1948T>C | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 3/6 | chr2 | 100404628 | |||||||
| chr2:100404673 | C | T | 36 | a0001c0001t0003g0005 a0001c0001t0003g0007 a0001c0001t0003g0023 others(33): Show |
82 | HG00423.hp1 HG00544.hp2 HG00735.hp1 others(79): Show |
intron_variant | MODIFIER | c.100+1903G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 3/6 | chr2 | 100404673 | |||||||
| chr2:100404704 | A | G | 1 | a0001c0001t0002g0161 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.100+1872T>C | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 3/6 | chr2 | 100404704 | |||||||
| chr2:100404933 | G | A | 1 | a0001c0002t0001g0112 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.100+1643C>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 3/6 | chr2 | 100404933 | |||||||
| chr2:100405155 | C | A | 1 | a0001c0001t0006g0080 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.100+1421G>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 3/6 | chr2 | 100405155 | |||||||
| chr2:100405172 | G | C | 1 | a0001c0001t0002g0048 | 2 | NA18997.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.100+1404C>G | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 3/6 | chr2 | 100405172 | |||||||
| chr2:100405305 | G | C | 1 | a0001c0001t0002g0155 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.100+1271C>G | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 3/6 | chr2 | 100405305 | |||||||
| chr2:100405355 | C | G | 2 | a0001c0001t0018g0051 a0001c0001t0019g0052 |
2 | HG04184.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.100+1221G>C | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 3/6 | chr2 | 100405355 | |||||||
| chr2:100405537 | C | G | 4 | a0001c0002t0001g0025 a0001c0002t0001g0083 a0002c0009t0001g0042 others(1): Show |
7 | HG01168.hp2 HG01169.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.100+1039G>C | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 3/6 | chr2 | 100405537 | |||||||
| chr2:100405552 | A | G | 40 | a0001c0001t0003g0005 a0001c0001t0003g0007 a0001c0001t0003g0023 others(37): Show |
89 | HG00423.hp1 HG00544.hp2 HG00735.hp1 others(86): Show |
intron_variant | MODIFIER | c.100+1024T>C | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 3/6 | chr2 | 100405552 | |||||||
| chr2:100405663 | A | G | 6 | a0001c0001t0006g0033 a0001c0001t0006g0079 a0001c0001t0006g0080 others(3): Show |
8 | HG01884.hp1 HG01891.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.100+913T>C | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 3/6 | chr2 | 100405663 | |||||||
| chr2:100405702 | T | A | 8 | a0001c0001t0004g0004 a0001c0001t0004g0028 a0001c0001t0004g0040 others(5): Show |
23 | HG01516.hp1 HG02055.hp1 HG02109.hp2 others(20): Show |
intron_variant | MODIFIER | c.100+874A>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 3/6 | chr2 | 100405702 | |||||||
| chr2:100405807 | T | C | 1 | a0002c0009t0001g0042 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.100+769A>G | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 3/6 | chr2 | 100405807 | |||||||
| chr2:100405809 | G | C | 1 | a0001c0001t0008g0156 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.100+767C>G | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 3/6 | chr2 | 100405809 | |||||||
| chr2:100405810 | C | T | 23 | a0001c0001t0003g0005 a0001c0001t0003g0007 a0001c0001t0003g0023 others(20): Show |
60 | HG00735.hp1 HG00741.hp2 HG01167.hp2 others(57): Show |
intron_variant | MODIFIER | c.100+766G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 3/6 | chr2 | 100405810 | |||||||
| chr2:100405826 | A | G | 1 | a0001c0014t0004g0118 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.100+750T>C | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 3/6 | chr2 | 100405826 | |||||||
| chr2:100405887 | A | G | 1 | a0001c0002t0001g0104 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.100+689T>C | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 3/6 | chr2 | 100405887 | |||||||
| chr2:100405948 | G | T | 36 | a0001c0001t0003g0005 a0001c0001t0003g0007 a0001c0001t0003g0023 others(33): Show |
82 | HG00423.hp1 HG00544.hp2 HG00735.hp1 others(79): Show |
intron_variant | MODIFIER | c.100+628C>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 3/6 | chr2 | 100405948 | |||||||
| chr2:100406037 | G | A | 8 | a0001c0001t0004g0004 a0001c0001t0004g0028 a0001c0001t0004g0040 others(5): Show |
23 | HG01516.hp1 HG02055.hp1 HG02109.hp2 others(20): Show |
intron_variant | MODIFIER | c.100+539C>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 3/6 | chr2 | 100406037 | |||||||
| chr2:100406047 | C | T | 2 | a0001c0001t0018g0051 a0001c0001t0019g0052 |
2 | HG04184.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.100+529G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 3/6 | chr2 | 100406047 | |||||||
| chr2:100406177 | G | A | 1 | a0002c0009t0001g0042 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.100+399C>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 3/6 | chr2 | 100406177 | |||||||
| chr2:100406233 | T | C | 3 | a0001c0003t0007g0008 a0001c0003t0007g0075 a0001c0003t0007g0078 |
11 | HG00423.hp1 HG00544.hp2 HG02056.hp1 others(8): Show |
intron_variant | MODIFIER | c.100+343A>G | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 3/6 | chr2 | 100406233 | |||||||
| chr2:100406264 | G | A | 67 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0021 others(64): Show |
132 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.100+312C>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 3/6 | chr2 | 100406264 | |||||||
| chr2:100406272 | T | C | 1 | a0001c0002t0001g0113 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.100+304A>G | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 3/6 | chr2 | 100406272 | |||||||
| chr2:100406319 | C | T | 2 | a0001c0001t0018g0051 a0001c0001t0019g0052 |
2 | HG04184.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.100+257G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 3/6 | chr2 | 100406319 | |||||||
| chr2:100406424 | C | T | 67 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0021 others(64): Show |
132 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.100+152G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 3/6 | chr2 | 100406424 | |||||||
| chr2:100406483 | C | G | 2 | a0001c0001t0018g0051 a0001c0001t0019g0052 |
2 | HG04184.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.100+93G>C | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 3/6 | chr2 | 100406483 | |||||||
| chr2:100406501 | A | G | 40 | a0001c0001t0003g0005 a0001c0001t0003g0007 a0001c0001t0003g0023 others(37): Show |
89 | HG00423.hp1 HG00544.hp2 HG00735.hp1 others(86): Show |
intron_variant | MODIFIER | c.100+75T>C | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 3/6 | chr2 | 100406501 | |||||||
| chr2:100406799 | T | A | 3 | a0001c0001t0002g0021 a0001c0001t0002g0043 a0001c0001t0002g0122 |
7 | HG00597.hp1 NA18945.hp1 NA18963.hp2 others(4): Show |
intron_variant | MODIFIER | c.-32-92A>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100406799 | |||||||
| chr2:100406867 | C | T | 36 | a0001c0001t0003g0005 a0001c0001t0003g0007 a0001c0001t0003g0023 others(33): Show |
82 | HG00423.hp1 HG00544.hp2 HG00735.hp1 others(79): Show |
intron_variant | MODIFIER | c.-32-160G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100406867 | |||||||
| chr2:100407060 | T | C | 1 | a0001c0002t0001g0114 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-32-353A>G | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100407060 | |||||||
| chr2:100407091 | G | T | 1 | a0001c0004t0002g0136 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.-32-384C>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100407091 | |||||||
| chr2:100407104 | G | A | 1 | a0001c0002t0001g0102 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-32-397C>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100407104 | |||||||
| chr2:100407114 | A | G | 2 | a0001c0001t0018g0051 a0001c0001t0019g0052 |
2 | HG04184.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.-32-407T>C | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100407114 | |||||||
| chr2:100407173 | G | A | 67 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0021 others(64): Show |
132 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.-32-466C>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100407173 | |||||||
| chr2:100407237 | C | T | 36 | a0001c0001t0003g0005 a0001c0001t0003g0007 a0001c0001t0003g0023 others(33): Show |
82 | HG00423.hp1 HG00544.hp2 HG00735.hp1 others(79): Show |
intron_variant | MODIFIER | c.-32-530G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100407237 | |||||||
| chr2:100407605 | G | C | 1 | a0001c0001t0002g0158 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-32-898C>G | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100407605 | |||||||
| chr2:100407691 | C | T | 1 | a0001c0001t0004g0040 | 2 | HG03195.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-32-984G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100407691 | |||||||
| chr2:100407717 | A | T | 1 | a0001c0001t0002g0135 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.-32-1010T>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100407717 | |||||||
| chr2:100407743 | G | A | 6 | a0002c0005t0009g0031 a0002c0005t0009g0059 a0002c0005t0010g0055 others(3): Show |
7 | HG02257.hp1 HG02717.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.-32-1036C>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100407743 | |||||||
| chr2:100407848 | G | A | 1 | a0001c0002t0001g0088 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.-32-1141C>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100407848 | |||||||
| chr2:100407922 | C | A | 3 | a0001c0001t0005g0016 a0001c0001t0005g0061 a0001c0001t0005g0066 |
3 | HG01167.hp2 HG03486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-32-1215G>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100407922 | |||||||
| chr2:100407951 | C | T | 36 | a0001c0001t0003g0005 a0001c0001t0003g0007 a0001c0001t0003g0023 others(33): Show |
82 | HG00423.hp1 HG00544.hp2 HG00735.hp1 others(79): Show |
intron_variant | MODIFIER | c.-32-1244G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100407951 | |||||||
| chr2:100407976 | C | T | 5 | a0001c0003t0007g0008 a0001c0003t0007g0075 a0001c0003t0007g0078 others(2): Show |
13 | HG00423.hp1 HG00544.hp2 HG02056.hp1 others(10): Show |
intron_variant | MODIFIER | c.-32-1269G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100407976 | |||||||
| chr2:100408010 | C | G | 1 | a0001c0001t0005g0062 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-32-1303G>C | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100408010 | |||||||
| chr2:100408130 | TTAGTA | T | 36 | a0001c0001t0003g0005 a0001c0001t0003g0007 a0001c0001t0003g0023 others(33): Show |
82 | HG00423.hp1 HG00544.hp2 HG00735.hp1 others(79): Show |
intron_variant | MODIFIER | c.-32-1428_-32-1424d others(7): Show |
CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100408130 | |||||||
| chr2:100408170 | T | TA | 10 | a0001c0002t0001g0025 a0001c0002t0001g0083 a0001c0003t0007g0008 others(7): Show |
21 | HG00423.hp1 HG00544.hp2 HG01168.hp2 others(18): Show |
intron_variant | MODIFIER | c.-32-1464dupT | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100408170 | |||||||
| chr2:100408226 | G | A | 1 | a0001c0002t0001g0116 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-32-1519C>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100408226 | |||||||
| chr2:100408261 | A | AG | 36 | a0001c0001t0003g0005 a0001c0001t0003g0007 a0001c0001t0003g0023 others(33): Show |
82 | HG00423.hp1 HG00544.hp2 HG00735.hp1 others(79): Show |
intron_variant | MODIFIER | c.-32-1555dupC | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100408261 | |||||||
| chr2:100408273 | A | G | 68 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0021 others(65): Show |
133 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.-32-1566T>C | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100408273 | |||||||
| chr2:100408321 | C | A | 1 | a0001c0001t0012g0128 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-32-1614G>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100408321 | |||||||
| chr2:100408476 | C | G | 2 | a0001c0001t0018g0051 a0001c0001t0019g0052 |
2 | HG04184.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.-32-1769G>C | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100408476 | |||||||
| chr2:100408650 | G | A | 2 | a0002c0005t0009g0031 a0002c0005t0009g0059 |
3 | HG02896.hp2 HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-32-1943C>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100408650 | |||||||
| chr2:100408884 | C | A | 2 | a0001c0001t0004g0004 a0001c0001t0004g0120 |
13 | HG02055.hp1 HG02451.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.-32-2177G>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100408884 | |||||||
| chr2:100408927 | G | C | 23 | a0001c0001t0003g0005 a0001c0001t0003g0007 a0001c0001t0003g0023 others(20): Show |
60 | HG00735.hp1 HG00741.hp2 HG01167.hp2 others(57): Show |
intron_variant | MODIFIER | c.-32-2220C>G | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100408927 | |||||||
| chr2:100408943 | C | T | 1 | a0001c0001t0004g0028 | 3 | HG01516.hp1 HG02723.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-32-2236G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100408943 | |||||||
| chr2:100409073 | G | C | 40 | a0001c0001t0003g0005 a0001c0001t0003g0007 a0001c0001t0003g0023 others(37): Show |
89 | HG00423.hp1 HG00544.hp2 HG00735.hp1 others(86): Show |
intron_variant | MODIFIER | c.-32-2366C>G | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100409073 | |||||||
| chr2:100409081 | G | A | 3 | a0001c0001t0018g0051 a0001c0001t0019g0052 a0001c0002t0001g0103 |
3 | HG00140.hp1 HG04184.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.-32-2374C>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100409081 | |||||||
| chr2:100409104 | G | A | 1 | a0001c0001t0002g0159 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-32-2397C>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100409104 | |||||||
| chr2:100409106 | G | A | 20 | a0001c0002t0001g0002 a0001c0002t0001g0026 a0001c0002t0001g0027 others(17): Show |
48 | HG00609.hp1 HG00735.hp2 HG00738.hp2 others(45): Show |
intron_variant | MODIFIER | c.-32-2399C>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100409106 | |||||||
| chr2:100409201 | T | C | 1 | a0001c0001t0002g0160 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-32-2494A>G | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100409201 | |||||||
| chr2:100409349 | T | C | 40 | a0001c0001t0003g0005 a0001c0001t0003g0007 a0001c0001t0003g0023 others(37): Show |
89 | HG00423.hp1 HG00544.hp2 HG00735.hp1 others(86): Show |
intron_variant | MODIFIER | c.-32-2642A>G | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100409349 | |||||||
| chr2:100409483 | G | A | 2 | a0001c0001t0018g0051 a0001c0001t0019g0052 |
2 | HG04184.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.-32-2776C>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100409483 | |||||||
| chr2:100409590 | C | T | 2 | a0001c0001t0018g0051 a0001c0001t0019g0052 |
2 | HG04184.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.-32-2883G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100409590 | |||||||
| chr2:100409608 | C | T | 2 | a0002c0009t0001g0042 a0007c0013t0028g0077 |
3 | HG02896.hp1 HG02897.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-32-2901G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100409608 | |||||||
| chr2:100409862 | A | C | 1 | a0001c0002t0001g0167 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-32-3155T>G | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100409862 | |||||||
| chr2:100409986 | G | A | 1 | a0001c0011t0006g0076 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-32-3279C>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100409986 | |||||||
| chr2:100409986 | G | T | 1 | a0001c0001t0002g0134 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.-32-3279C>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100409986 | |||||||
| chr2:100410010 | G | A | 5 | a0001c0001t0004g0004 a0001c0001t0004g0041 a0001c0001t0004g0119 others(2): Show |
17 | HG02055.hp1 HG02451.hp2 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.-32-3303C>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100410010 | |||||||
| chr2:100410179 | G | A | 2 | a0001c0001t0018g0051 a0001c0001t0019g0052 |
2 | HG04184.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.-32-3472C>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100410179 | |||||||
| chr2:100410286 | T | C | 1 | a0001c0002t0001g0039 | 2 | HG03490.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.-32-3579A>G | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100410286 | |||||||
| chr2:100410391 | G | A | 1 | a0001c0001t0002g0161 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.-32-3684C>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100410391 | |||||||
| chr2:100410659 | T | C | 1 | a0001c0002t0001g0083 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-32-3952A>G | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100410659 | |||||||
| chr2:100410754 | T | C | 1 | a0001c0003t0007g0075 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.-32-4047A>G | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100410754 | |||||||
| chr2:100410765 | A | G | 1 | a0001c0002t0001g0093 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-32-4058T>C | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100410765 | |||||||
| chr2:100410818 | G | A | 2 | a0001c0001t0018g0051 a0001c0001t0019g0052 |
2 | HG04184.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.-32-4111C>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100410818 | |||||||
| chr2:100410938 | G | A | 37 | a0001c0001t0003g0005 a0001c0001t0003g0007 a0001c0001t0003g0023 others(34): Show |
83 | HG00423.hp1 HG00544.hp2 HG00735.hp1 others(80): Show |
intron_variant | MODIFIER | c.-33+4103C>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100410938 | |||||||
| chr2:100411116 | C | CT | 14 | a0001c0001t0002g0044 a0001c0001t0002g0126 a0001c0001t0002g0133 others(11): Show |
27 | HG01884.hp1 HG01928.hp1 HG02055.hp1 others(24): Show |
intron_variant | MODIFIER | c.-33+3924dupA | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100411116 | |||||||
| chr2:100411116 | C | CTT | 3 | a0001c0001t0004g0028 a0001c0001t0004g0040 a0006c0015t0004g0117 |
6 | HG01516.hp1 HG02109.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.-33+3923_-33+3924d others(4): Show |
CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100411116 | |||||||
| chr2:100411116 | CT | C | 25 | a0001c0001t0002g0131 a0001c0001t0003g0005 a0001c0001t0003g0007 others(22): Show |
68 | HG00423.hp1 HG00544.hp2 HG00735.hp1 others(65): Show |
intron_variant | MODIFIER | c.-33+3924delA | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100411116 | |||||||
| chr2:100411116 | CTT | C | 4 | a0001c0001t0005g0022 a0001c0001t0005g0067 a0001c0007t0003g0072 others(1): Show |
6 | HG02148.hp2 NA18941.hp1 NA18953.hp2 others(3): Show |
intron_variant | MODIFIER | c.-33+3923_-33+3924d others(4): Show |
CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100411116 | |||||||
| chr2:100411121 | T | C | 2 | a0001c0002t0001g0025 a0001c0002t0001g0083 |
4 | HG01168.hp2 HG01169.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.-33+3920A>G | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100411121 | |||||||
| chr2:100411247 | G | A | 1 | a0001c0001t0002g0163 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.-33+3794C>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100411247 | |||||||
| chr2:100411263 | C | T | 8 | a0001c0001t0004g0004 a0001c0001t0004g0028 a0001c0001t0004g0040 others(5): Show |
23 | HG01516.hp1 HG02055.hp1 HG02109.hp2 others(20): Show |
intron_variant | MODIFIER | c.-33+3778G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100411263 | |||||||
| chr2:100411295 | A | G | 1 | a0001c0001t0017g0050 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.-33+3746T>C | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100411295 | |||||||
| chr2:100411366 | A | C | 41 | a0001c0001t0003g0005 a0001c0001t0003g0007 a0001c0001t0003g0023 others(38): Show |
90 | HG00423.hp1 HG00544.hp2 HG00735.hp1 others(87): Show |
intron_variant | MODIFIER | c.-33+3675T>G | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100411366 | |||||||
| chr2:100411600 | C | T | 2 | a0001c0002t0001g0025 a0001c0002t0001g0083 |
4 | HG01168.hp2 HG01169.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.-33+3441G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100411600 | |||||||
| chr2:100411774 | G | T | 37 | a0001c0001t0003g0005 a0001c0001t0003g0007 a0001c0001t0003g0023 others(34): Show |
83 | HG00423.hp1 HG00544.hp2 HG00735.hp1 others(80): Show |
intron_variant | MODIFIER | c.-33+3267C>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100411774 | |||||||
| chr2:100411818 | C | T | 1 | a0001c0002t0001g0166 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-33+3223G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100411818 | |||||||
| chr2:100411845 | G | C | 2 | a0001c0001t0018g0051 a0001c0001t0019g0052 |
2 | HG04184.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.-33+3196C>G | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100411845 | |||||||
| chr2:100411909 | G | A | 2 | a0001c0001t0002g0043 a0001c0001t0002g0122 |
3 | NA18970.hp2 NA19001.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.-33+3132C>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100411909 | |||||||
| chr2:100411997 | G | C | 3 | a0001c0001t0005g0062 a0001c0001t0005g0063 a0001c0001t0005g0065 |
3 | HG02258.hp1 HG03471.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-33+3044C>G | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100411997 | |||||||
| chr2:100412259 | G | T | 1 | a0001c0001t0002g0132 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-33+2782C>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100412259 | |||||||
| chr2:100412262 | G | A | 1 | a0003c0008t0003g0070 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-33+2779C>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100412262 | |||||||
| chr2:100412291 | G | A | 1 | a0001c0001t0003g0071 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-33+2750C>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100412291 | |||||||
| chr2:100412329 | T | A | 3 | a0001c0001t0005g0062 a0001c0001t0005g0063 a0001c0001t0005g0065 |
3 | HG02258.hp1 HG03471.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-33+2712A>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100412329 | |||||||
| chr2:100412331 | C | T | 6 | a0001c0001t0006g0033 a0001c0001t0006g0079 a0001c0001t0006g0080 others(3): Show |
8 | HG01884.hp1 HG01891.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.-33+2710G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100412331 | |||||||
| chr2:100412376 | G | T | 1 | a0001c0001t0002g0131 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.-33+2665C>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100412376 | |||||||
| chr2:100412456 | G | A | 37 | a0001c0001t0003g0005 a0001c0001t0003g0007 a0001c0001t0003g0023 others(34): Show |
83 | HG00423.hp1 HG00544.hp2 HG00735.hp1 others(80): Show |
intron_variant | MODIFIER | c.-33+2585C>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100412456 | |||||||
| chr2:100412460 | TAC | T | 8 | a0001c0001t0004g0004 a0001c0001t0004g0028 a0001c0001t0004g0040 others(5): Show |
23 | HG01516.hp1 HG02055.hp1 HG02109.hp2 others(20): Show |
intron_variant | MODIFIER | c.-33+2579_-33+2580d others(4): Show |
CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100412460 | |||||||
| chr2:100412540 | G | A | 114 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0021 others(111): Show |
239 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(236): Show |
intron_variant | MODIFIER | c.-33+2501C>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100412540 | |||||||
| chr2:100412568 | C | T | 2 | a0001c0002t0001g0011 a0001c0002t0001g0088 |
6 | NA18951.hp2 NA18960.hp1 NA19005.hp2 others(3): Show |
intron_variant | MODIFIER | c.-33+2473G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100412568 | |||||||
| chr2:100412854 | A | C | 41 | a0001c0001t0003g0005 a0001c0001t0003g0007 a0001c0001t0003g0023 others(38): Show |
90 | HG00423.hp1 HG00544.hp2 HG00735.hp1 others(87): Show |
intron_variant | MODIFIER | c.-33+2187T>G | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100412854 | |||||||
| chr2:100412870 | C | T | 1 | a0001c0002t0001g0087 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-33+2171G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100412870 | |||||||
| chr2:100412982 | C | A | 1 | a0001c0002t0001g0084 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.-33+2059G>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100412982 | |||||||
| chr2:100413449 | G | A | 2 | a0001c0001t0005g0022 a0001c0001t0005g0067 |
4 | HG02148.hp2 NA18953.hp2 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.-33+1592C>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100413449 | |||||||
| chr2:100413543 | C | A | 2 | a0001c0002t0001g0115 a0001c0002t0001g0116 |
2 | HG02572.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-33+1498G>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100413543 | |||||||
| chr2:100413702 | A | C | 1 | a0001c0002t0001g0086 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-33+1339T>G | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100413702 | |||||||
| chr2:100413713 | C | T | 1 | a0007c0013t0028g0077 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-33+1328G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100413713 | |||||||
| chr2:100413810 | T | A | 1 | a0001c0001t0002g0164 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-33+1231A>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100413810 | |||||||
| chr2:100413947 | C | A | 1 | a0007c0013t0028g0077 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-33+1094G>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100413947 | |||||||
| chr2:100414019 | C | T | 2 | a0001c0001t0005g0022 a0001c0001t0005g0067 |
4 | HG02148.hp2 NA18953.hp2 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.-33+1022G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100414019 | |||||||
| chr2:100414130 | T | C | 2 | a0001c0002t0001g0025 a0001c0002t0001g0083 |
4 | HG01168.hp2 HG01169.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.-33+911A>G | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100414130 | |||||||
| chr2:100414282 | C | A | 1 | a0007c0013t0028g0077 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-33+759G>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100414282 | |||||||
| chr2:100414286 | C | T | 1 | a0001c0002t0001g0085 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.-33+755G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100414286 | |||||||
| chr2:100414362 | T | TCA | 14 | a0001c0001t0003g0005 a0001c0001t0003g0023 a0001c0001t0003g0024 others(11): Show |
33 | HG01243.hp1 HG01891.hp1 HG02148.hp2 others(30): Show |
intron_variant | MODIFIER | c.-33+677_-33+678dup others(2): Show |
CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100414362 | |||||||
| chr2:100414362 | T | TCACA | 7 | a0001c0001t0005g0015 a0001c0001t0005g0016 a0001c0001t0005g0061 others(4): Show |
14 | HG01167.hp2 HG01261.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.-33+675_-33+678dup others(4): Show |
CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100414362 | |||||||
| chr2:100414362 | T | TCACACA | 3 | a0001c0001t0005g0064 a0001c0001t0005g0065 a0007c0013t0028g0077 |
3 | HG03540.hp2 NA19240.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-33+673_-33+678dup others(6): Show |
CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100414362 | |||||||
| chr2:100414381 | C | CAA | 3 | a0001c0001t0003g0007 a0001c0007t0003g0018 a0001c0007t0003g0072 |
14 | HG00735.hp1 HG00741.hp2 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.-33+658_-33+659dup others(2): Show |
CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100414381 | |||||||
| chr2:100414676 | A | G | 1 | a0002c0009t0001g0042 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-33+365T>C | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100414676 | |||||||
| chr2:100414679 | C | G | 1 | a0001c0001t0002g0130 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-33+362G>C | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100414679 | |||||||
| chr2:100414885 | C | T | 7 | a0001c0002t0001g0060 a0002c0005t0009g0031 a0002c0005t0009g0059 others(4): Show |
8 | HG02257.hp1 HG02717.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.-33+156G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100414885 | |||||||
| chr2:100414903 | T | C | 1 | a0001c0003t0007g0078 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-33+138A>G | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100414903 | |||||||
| chr2:100414988 | A | T | 1 | a0001c0001t0002g0129 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.-33+53T>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 2/6 | chr2 | 100414988 | |||||||
| chr2:100415112 | C | T | 3 | a0001c0002t0001g0026 a0001c0002t0001g0121 a0001c0002t0020g0053 |
5 | NA18972.hp2 NA18980.hp1 NA19003.hp1 others(2): Show |
splice_acceptor_variant&intron_variant | HIGH | c.-103-1G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 1/6 | chr2 | 100415112 | |||||||
| chr2:100415127 | A | T | 1 | a0002c0005t0027g0058 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-103-16T>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 1/6 | chr2 | 100415127 | |||||||
| chr2:100415278 | T | G | 1 | a0001c0001t0002g0043 | 2 | NA18970.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.-103-167A>C | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 1/6 | chr2 | 100415278 | |||||||
| chr2:100415303 | C | CA | 3 | a0001c0001t0005g0016 a0001c0001t0005g0061 a0001c0001t0005g0066 |
6 | HG01167.hp2 HG02622.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-103-193dupT | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 1/6 | chr2 | 100415303 | |||||||
| chr2:100415403 | G | A | 49 | a0001c0001t0003g0005 a0001c0001t0003g0007 a0001c0001t0003g0023 others(46): Show |
113 | HG00423.hp1 HG00544.hp2 HG00735.hp1 others(110): Show |
intron_variant | MODIFIER | c.-103-292C>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 1/6 | chr2 | 100415403 | |||||||
| chr2:100415628 | A | G | 1 | a0001c0002t0001g0084 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.-103-517T>C | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 1/6 | chr2 | 100415628 | |||||||
| chr2:100415630 | C | G | 2 | a0001c0002t0001g0025 a0001c0002t0001g0083 |
4 | HG01168.hp2 HG01169.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.-103-519G>C | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 1/6 | chr2 | 100415630 | |||||||
| chr2:100415638 | G | A | 1 | a0001c0001t0005g0067 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.-103-527C>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 1/6 | chr2 | 100415638 | |||||||
| chr2:100415757 | C | T | 2 | a0001c0001t0012g0127 a0001c0001t0012g0128 |
2 | HG01192.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.-103-646G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 1/6 | chr2 | 100415757 | |||||||
| chr2:100415917 | C | T | 4 | a0001c0001t0002g0021 a0001c0001t0002g0043 a0001c0001t0002g0122 others(1): Show |
8 | HG00597.hp1 NA18945.hp1 NA18963.hp2 others(5): Show |
intron_variant | MODIFIER | c.-103-806G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 1/6 | chr2 | 100415917 | |||||||
| chr2:100415921 | C | T | 2 | a0001c0001t0002g0124 a0001c0001t0002g0125 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-103-810G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 1/6 | chr2 | 100415921 | |||||||
| chr2:100416035 | T | C | 1 | a0002c0009t0001g0042 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-103-924A>G | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 1/6 | chr2 | 100416035 | |||||||
| chr2:100416083 | C | T | 1 | a0001c0001t0017g0050 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.-103-972G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 1/6 | chr2 | 100416083 | |||||||
| chr2:100416153 | T | G | 1 | a0001c0001t0003g0073 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-103-1042A>C | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 1/6 | chr2 | 100416153 | |||||||
| chr2:100416253 | A | C | 23 | a0001c0001t0003g0005 a0001c0001t0003g0007 a0001c0001t0003g0023 others(20): Show |
60 | HG00735.hp1 HG00741.hp2 HG01167.hp2 others(57): Show |
intron_variant | MODIFIER | c.-104+1121T>G | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 1/6 | chr2 | 100416253 | |||||||
| chr2:100416283 | C | T | 65 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0021 others(62): Show |
126 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(123): Show |
intron_variant | MODIFIER | c.-104+1091G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 1/6 | chr2 | 100416283 | |||||||
| chr2:100416354 | A | G | 37 | a0001c0001t0003g0005 a0001c0001t0003g0007 a0001c0001t0003g0023 others(34): Show |
84 | HG00423.hp1 HG00544.hp2 HG00735.hp1 others(81): Show |
intron_variant | MODIFIER | c.-104+1020T>C | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 1/6 | chr2 | 100416354 | |||||||
| chr2:100416467 | T | C | 1 | a0002c0009t0001g0042 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-104+907A>G | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 1/6 | chr2 | 100416467 | |||||||
| chr2:100416688 | A | AAAC | 14 | a0001c0001t0002g0122 a0001c0001t0003g0005 a0001c0001t0003g0007 others(11): Show |
42 | HG00735.hp1 HG00741.hp2 HG01243.hp1 others(39): Show |
intron_variant | MODIFIER | c.-104+683_-104+685d others(5): Show |
CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 1/6 | chr2 | 100416688 | |||||||
| chr2:100416688 | A | AAACAAC | 13 | a0001c0001t0005g0015 a0001c0001t0005g0016 a0001c0001t0005g0022 others(10): Show |
22 | HG01167.hp2 HG01261.hp2 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.-104+680_-104+685d others(8): Show |
CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 1/6 | chr2 | 100416688 | |||||||
| chr2:100416688 | A | AAACAACA others(2): Show |
7 | a0001c0001t0005g0061 a0002c0005t0009g0031 a0002c0005t0009g0059 others(4): Show |
8 | HG02257.hp1 HG02717.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.-104+677_-104+685d others(11): Show |
CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 1/6 | chr2 | 100416688 | |||||||
| chr2:100417117 | T | C | 1 | a0001c0002t0001g0121 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.-104+257A>G | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 1/6 | chr2 | 100417117 | |||||||
| chr2:100417205 | C | T | 7 | a0001c0002t0001g0060 a0002c0005t0009g0031 a0002c0005t0009g0059 others(4): Show |
8 | HG02257.hp1 HG02717.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.-104+169G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 1/6 | chr2 | 100417205 | |||||||
| chr2:100417235 | G | A | 59 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0021 others(56): Show |
118 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(115): Show |
intron_variant | MODIFIER | c.-104+139C>T | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 1/6 | chr2 | 100417235 | |||||||
| chr2:100417294 | C | T | 164 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0021 others(161): Show |
358 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(355): Show |
intron_variant | MODIFIER | c.-104+80G>A | CHST10 | ENSG00000115526.11 | transcript | ENST00000264249.8 | protein_coding | 1/6 | chr2 | 100417294 |