Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 64132 |
| ensemblid | ENSG00000015532.10 |
| hgncid | 15517 |
| symbol | XYLT2 |
| name | xylosyltransferase 2 |
| refseq_nuc | NM_022167.4 |
| refseq_prot | NP_071450.2 |
| ensembl_nuc | ENST00000017003.7 |
| ensembl_prot | ENSP00000017003.2 |
| mane_status | MANE Select |
| chr | chr17 |
| start | 50346126 |
| end | 50361185 |
| strand | + |
| ver | v1.2 |
| region | chr17:50346126-50361185 |
| region5000 | chr17:50341126-50366185 |
| regionname0 | XYLT2_chr17_50346126_50361185 |
| regionname5000 | XYLT2_chr17_50341126_50366185 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 865 | 205 | 56 | 31 | 80 | 7 | 30 | 64 | XYLT2_chr17_50341126_50366185 | XYLT2 | MVASA others(860): Show |
chr17 | 50341126 | 50366185 |
| a0002 | 0/1 | 865 | 74 | 18 | 19 | 20 | 4 | 12 | 15 | XYLT2_chr17_50341126_50366185 | XYLT2 | MVASA others(860): Show |
chr17 | 50341126 | 50366185 |
| a0003 | 0/0 | 865 | 52 | 1 | 22 | 23 | 4 | 2 | 17 | XYLT2_chr17_50341126_50366185 | XYLT2 | MVASA others(860): Show |
chr17 | 50341126 | 50366185 |
| a0004 | 0/0 | 865 | 9 | 6 | 3 | 0 | 0 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | MVASA others(860): Show |
chr17 | 50341126 | 50366185 |
| a0005 | 0/0 | 865 | 6 | 5 | 1 | 0 | 0 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | MVASA others(860): Show |
chr17 | 50341126 | 50366185 |
| a0006 | 0/0 | 865 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | MVASA others(860): Show |
chr17 | 50341126 | 50366185 |
| a0007 | 0/0 | 865 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | MVASA others(860): Show |
chr17 | 50341126 | 50366185 |
| a0008 | 0/0 | 865 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | MVASA others(860): Show |
chr17 | 50341126 | 50366185 |
| a0009 | 0/0 | 865 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | MVASA others(860): Show |
chr17 | 50341126 | 50366185 |
| a0010 | 0/0 | 865 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | MVASA others(860): Show |
chr17 | 50341126 | 50366185 |
| a0011 | 0/0 | 865 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | MVASA others(860): Show |
chr17 | 50341126 | 50366185 |
| a0012 | 0/0 | 865 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | MVASA others(860): Show |
chr17 | 50341126 | 50366185 |
| a0013 | 0/0 | 865 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | MVASA others(860): Show |
chr17 | 50341126 | 50366185 |
| a0014 | 0/0 | 865 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | MVASA others(860): Show |
chr17 | 50341126 | 50366185 |
| a0015 | 0/0 | 865 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | MVASA others(860): Show |
chr17 | 50341126 | 50366185 |
| a0016 | 0/0 | 865 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | XYLT2_chr17_50341126_50366185 | XYLT2 | MVASA others(860): Show |
chr17 | 50341126 | 50366185 |
| a0017 | 0/0 | 865 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | XYLT2_chr17_50341126_50366185 | XYLT2 | MVASA others(860): Show |
chr17 | 50341126 | 50366185 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 2595 | 102 | 21 | 4 | 56 | 1 | 19 | XYLT2_chr17_50341126_50366185 | XYLT2 | ATGGT others(2590): Show |
chr17 | 50341126 | 50366185 | ||
| a0001c0003 | 0/0 | 2595 | 58 | 17 | 20 | 4 | 6 | 11 | XYLT2_chr17_50341126_50366185 | XYLT2 | ATGGT others(2590): Show |
chr17 | 50341126 | 50366185 | ||
| a0001c0005 | 0/0 | 2595 | 18 | 18 | 0 | 0 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | ATGGT others(2590): Show |
chr17 | 50341126 | 50366185 | ||
| a0001c0006 | 0/0 | 2595 | 13 | 0 | 0 | 13 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | ATGGT others(2590): Show |
chr17 | 50341126 | 50366185 | ||
| a0001c0008 | 0/0 | 2595 | 7 | 0 | 7 | 0 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | ATGGT others(2590): Show |
chr17 | 50341126 | 50366185 | ||
| a0001c0010 | 0/0 | 2595 | 6 | 0 | 0 | 6 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | ATGGT others(2590): Show |
chr17 | 50341126 | 50366185 | ||
| a0001c0026 | 0/0 | 2595 | 1 | 0 | 0 | 1 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | ATGGT others(2590): Show |
chr17 | 50341126 | 50366185 | ||
| a0002c0002 | 0/1 | 2595 | 72 | 18 | 19 | 19 | 4 | 11 | XYLT2_chr17_50341126_50366185 | XYLT2 | ATGGT others(2590): Show |
chr17 | 50341126 | 50366185 | ||
| a0002c0017 | 0/0 | 2595 | 1 | 0 | 0 | 1 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | ATGGT others(2590): Show |
chr17 | 50341126 | 50366185 | ||
| a0002c0027 | 0/0 | 2595 | 1 | 0 | 0 | 0 | 0 | 1 | XYLT2_chr17_50341126_50366185 | XYLT2 | ATGGT others(2590): Show |
chr17 | 50341126 | 50366185 | ||
| a0003c0004 | 0/0 | 2595 | 50 | 1 | 22 | 21 | 4 | 2 | XYLT2_chr17_50341126_50366185 | XYLT2 | ATGGT others(2590): Show |
chr17 | 50341126 | 50366185 | ||
| a0003c0014 | 0/0 | 2595 | 1 | 0 | 0 | 1 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | ATGGT others(2590): Show |
chr17 | 50341126 | 50366185 | ||
| a0003c0015 | 0/0 | 2595 | 1 | 0 | 0 | 1 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | ATGGT others(2590): Show |
chr17 | 50341126 | 50366185 | ||
| a0004c0007 | 0/0 | 2595 | 9 | 6 | 3 | 0 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | ATGGT others(2590): Show |
chr17 | 50341126 | 50366185 | ||
| a0005c0009 | 0/0 | 2595 | 6 | 5 | 1 | 0 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | ATGGT others(2590): Show |
chr17 | 50341126 | 50366185 | ||
| a0006c0011 | 0/0 | 2595 | 2 | 0 | 2 | 0 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | ATGGT others(2590): Show |
chr17 | 50341126 | 50366185 | ||
| a0007c0012 | 0/0 | 2595 | 2 | 2 | 0 | 0 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | ATGGT others(2590): Show |
chr17 | 50341126 | 50366185 | ||
| a0008c0024 | 0/0 | 2595 | 1 | 0 | 0 | 0 | 1 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | ATGGT others(2590): Show |
chr17 | 50341126 | 50366185 | ||
| a0009c0018 | 0/0 | 2595 | 1 | 0 | 0 | 1 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | ATGGT others(2590): Show |
chr17 | 50341126 | 50366185 | ||
| a0010c0022 | 0/0 | 2595 | 1 | 1 | 0 | 0 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | ATGGT others(2590): Show |
chr17 | 50341126 | 50366185 | ||
| a0011c0025 | 0/0 | 2595 | 1 | 0 | 0 | 0 | 0 | 1 | XYLT2_chr17_50341126_50366185 | XYLT2 | ATGGT others(2590): Show |
chr17 | 50341126 | 50366185 | ||
| a0012c0016 | 0/0 | 2595 | 1 | 1 | 0 | 0 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | ATGGT others(2590): Show |
chr17 | 50341126 | 50366185 | ||
| a0013c0019 | 0/0 | 2595 | 1 | 1 | 0 | 0 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | ATGGT others(2590): Show |
chr17 | 50341126 | 50366185 | ||
| a0014c0013 | 0/0 | 2595 | 1 | 0 | 0 | 0 | 0 | 1 | XYLT2_chr17_50341126_50366185 | XYLT2 | ATGGT others(2590): Show |
chr17 | 50341126 | 50366185 | ||
| a0015c0021 | 0/0 | 2595 | 1 | 1 | 0 | 0 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | ATGGT others(2590): Show |
chr17 | 50341126 | 50366185 | ||
| a0016c0020 | 0/0 | 2595 | 1 | 0 | 0 | 1 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | ATGGT others(2590): Show |
chr17 | 50341126 | 50366185 | ||
| a0017c0023 | 0/0 | 2595 | 1 | 0 | 0 | 1 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | ATGGT others(2590): Show |
chr17 | 50341126 | 50366185 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3507 | 81 | 6 | 4 | 51 | 1 | 19 | XYLT2_chr17_50341126_50366185 | XYLT2 | GTCCC others(3502): Show |
chr17 | 50341126 | 50366185 |
| a0001c0001t0004 | 1/0 | 3507 | 15 | 14 | 0 | 0 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | GTCCC others(3502): Show |
chr17 | 50341126 | 50366185 |
| a0001c0001t0006 | 0/0 | 3508 | 5 | 1 | 0 | 4 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | GTCCC others(3503): Show |
chr17 | 50341126 | 50366185 |
| a0001c0001t0012 | 0/0 | 3507 | 1 | 0 | 0 | 1 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | GTCCC others(3502): Show |
chr17 | 50341126 | 50366185 |
| a0001c0003t0002 | 0/0 | 3507 | 50 | 13 | 19 | 4 | 6 | 8 | XYLT2_chr17_50341126_50366185 | XYLT2 | GTCCC others(3502): Show |
chr17 | 50341126 | 50366185 |
| a0001c0003t0003 | 0/0 | 3508 | 1 | 0 | 0 | 0 | 0 | 1 | XYLT2_chr17_50341126_50366185 | XYLT2 | GTCCC others(3503): Show |
chr17 | 50341126 | 50366185 |
| a0001c0003t0004 | 0/0 | 3507 | 4 | 4 | 0 | 0 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | GTCCC others(3502): Show |
chr17 | 50341126 | 50366185 |
| a0001c0003t0009 | 0/0 | 3507 | 2 | 0 | 1 | 0 | 0 | 1 | XYLT2_chr17_50341126_50366185 | XYLT2 | GTCCC others(3502): Show |
chr17 | 50341126 | 50366185 |
| a0001c0003t0016 | 0/0 | 3507 | 1 | 0 | 0 | 0 | 0 | 1 | XYLT2_chr17_50341126_50366185 | XYLT2 | GTCCC others(3502): Show |
chr17 | 50341126 | 50366185 |
| a0001c0005t0004 | 0/0 | 3507 | 16 | 16 | 0 | 0 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | GTCCC others(3502): Show |
chr17 | 50341126 | 50366185 |
| a0001c0005t0011 | 0/0 | 3507 | 2 | 2 | 0 | 0 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | GTCCC others(3502): Show |
chr17 | 50341126 | 50366185 |
| a0001c0006t0001 | 0/0 | 3507 | 13 | 0 | 0 | 13 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | GTCCC others(3502): Show |
chr17 | 50341126 | 50366185 |
| a0001c0008t0001 | 0/0 | 3507 | 7 | 0 | 7 | 0 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | GTCCC others(3502): Show |
chr17 | 50341126 | 50366185 |
| a0001c0010t0001 | 0/0 | 3507 | 6 | 0 | 0 | 6 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | GTCCC others(3502): Show |
chr17 | 50341126 | 50366185 |
| a0001c0026t0001 | 0/0 | 3507 | 1 | 0 | 0 | 1 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | GTCCC others(3502): Show |
chr17 | 50341126 | 50366185 |
| a0002c0002t0001 | 0/0 | 3507 | 69 | 17 | 19 | 19 | 4 | 10 | XYLT2_chr17_50341126_50366185 | XYLT2 | GTCCC others(3502): Show |
chr17 | 50341126 | 50366185 |
| a0002c0002t0015 | 0/0 | 3507 | 1 | 1 | 0 | 0 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | GTCCC others(3502): Show |
chr17 | 50341126 | 50366185 |
| a0002c0002t0017 | 0/0 | 3507 | 1 | 0 | 0 | 0 | 0 | 1 | XYLT2_chr17_50341126_50366185 | XYLT2 | GTCCC others(3502): Show |
chr17 | 50341126 | 50366185 |
| a0002c0002t0018 | 0/1 | 3508 | 1 | 0 | 0 | 0 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | GTCCC others(3503): Show |
chr17 | 50341126 | 50366185 |
| a0002c0017t0001 | 0/0 | 3507 | 1 | 0 | 0 | 1 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | GTCCC others(3502): Show |
chr17 | 50341126 | 50366185 |
| a0002c0027t0001 | 0/0 | 3507 | 1 | 0 | 0 | 0 | 0 | 1 | XYLT2_chr17_50341126_50366185 | XYLT2 | GTCCC others(3502): Show |
chr17 | 50341126 | 50366185 |
| a0003c0004t0003 | 0/0 | 3508 | 45 | 1 | 20 | 18 | 4 | 2 | XYLT2_chr17_50341126_50366185 | XYLT2 | GTCCC others(3503): Show |
chr17 | 50341126 | 50366185 |
| a0003c0004t0008 | 0/0 | 3507 | 2 | 0 | 1 | 1 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | GTCCC others(3502): Show |
chr17 | 50341126 | 50366185 |
| a0003c0004t0013 | 0/0 | 3508 | 1 | 0 | 0 | 1 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | GTCCC others(3503): Show |
chr17 | 50341126 | 50366185 |
| a0003c0004t0014 | 0/0 | 3508 | 1 | 0 | 0 | 1 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | GTCCC others(3503): Show |
chr17 | 50341126 | 50366185 |
| a0003c0004t0021 | 0/0 | 3508 | 1 | 0 | 1 | 0 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | GTCCC others(3503): Show |
chr17 | 50341126 | 50366185 |
| a0003c0014t0008 | 0/0 | 3507 | 1 | 0 | 0 | 1 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | GTCCC others(3502): Show |
chr17 | 50341126 | 50366185 |
| a0003c0015t0003 | 0/0 | 3508 | 1 | 0 | 0 | 1 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | GTCCC others(3503): Show |
chr17 | 50341126 | 50366185 |
| a0004c0007t0004 | 0/0 | 3507 | 6 | 3 | 3 | 0 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | GTCCC others(3502): Show |
chr17 | 50341126 | 50366185 |
| a0004c0007t0007 | 0/0 | 3507 | 3 | 3 | 0 | 0 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | GTCCC others(3502): Show |
chr17 | 50341126 | 50366185 |
| a0005c0009t0005 | 0/0 | 3507 | 6 | 5 | 1 | 0 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | GTCCC others(3502): Show |
chr17 | 50341126 | 50366185 |
| a0006c0011t0001 | 0/0 | 3507 | 2 | 0 | 2 | 0 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | GTCCC others(3502): Show |
chr17 | 50341126 | 50366185 |
| a0007c0012t0010 | 0/0 | 3507 | 2 | 2 | 0 | 0 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | GTCCC others(3502): Show |
chr17 | 50341126 | 50366185 |
| a0008c0024t0001 | 0/0 | 3507 | 1 | 0 | 0 | 0 | 1 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | GTCCC others(3502): Show |
chr17 | 50341126 | 50366185 |
| a0009c0018t0001 | 0/0 | 3507 | 1 | 0 | 0 | 1 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | GTCCC others(3502): Show |
chr17 | 50341126 | 50366185 |
| a0010c0022t0007 | 0/0 | 3507 | 1 | 1 | 0 | 0 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | GTCCC others(3502): Show |
chr17 | 50341126 | 50366185 |
| a0011c0025t0005 | 0/0 | 3507 | 1 | 0 | 0 | 0 | 0 | 1 | XYLT2_chr17_50341126_50366185 | XYLT2 | GTCCC others(3502): Show |
chr17 | 50341126 | 50366185 |
| a0012c0016t0020 | 0/0 | 3507 | 1 | 1 | 0 | 0 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | GTCCC others(3502): Show |
chr17 | 50341126 | 50366185 |
| a0013c0019t0002 | 0/0 | 3507 | 1 | 1 | 0 | 0 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | GTCCC others(3502): Show |
chr17 | 50341126 | 50366185 |
| a0014c0013t0003 | 0/0 | 3508 | 1 | 0 | 0 | 0 | 0 | 1 | XYLT2_chr17_50341126_50366185 | XYLT2 | GTCCC others(3503): Show |
chr17 | 50341126 | 50366185 |
| a0015c0021t0019 | 0/0 | 3507 | 1 | 1 | 0 | 0 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | GTCCC others(3502): Show |
chr17 | 50341126 | 50366185 |
| a0016c0020t0002 | 0/0 | 3507 | 1 | 0 | 0 | 1 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | GTCCC others(3502): Show |
chr17 | 50341126 | 50366185 |
| a0017c0023t0001 | 0/0 | 3507 | 1 | 0 | 0 | 1 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | GTCCC others(3502): Show |
chr17 | 50341126 | 50366185 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 54 | 1 | 4 | 40 | 1 | 8 | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| a0001c0001t0001g0013 | 0/0 | 4 | 0 | 0 | 2 | 0 | 2 | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| a0001c0001t0001g0015 | 0/0 | 4 | 0 | 0 | 0 | 0 | 4 | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| a0001c0001t0001g0020 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| a0001c0001t0001g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| a0001c0001t0004g0011 | 1/0 | 4 | 3 | 0 | 0 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| a0001c0001t0004g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| a0001c0001t0004g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| a0001c0001t0004g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| a0001c0001t0004g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| a0001c0001t0004g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| a0001c0001t0004g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| a0001c0001t0004g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| a0001c0001t0004g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| a0001c0001t0004g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| a0001c0001t0006g0001 | 0/0 | 5 | 1 | 0 | 4 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| a0001c0001t0012g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| a0001c0003t0002g0003 | 0/0 | 18 | 0 | 11 | 0 | 3 | 4 | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| a0001c0003t0002g0006 | 0/0 | 12 | 8 | 4 | 0 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| a0001c0003t0002g0009 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| a0001c0003t0002g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| a0001c0003t0002g0021 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| a0001c0003t0002g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| a0001c0003t0002g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| a0001c0003t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| a0001c0003t0002g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| a0001c0003t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| a0001c0003t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| a0001c0003t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| a0001c0003t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| a0001c0003t0002g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| a0001c0003t0003g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| a0001c0003t0004g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| a0001c0003t0004g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| a0001c0003t0004g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| a0001c0003t0004g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| a0001c0003t0009g0003 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| a0001c0003t0016g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| a0001c0005t0004g0005 | 0/0 | 14 | 14 | 0 | 0 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| a0001c0005t0004g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| a0001c0005t0004g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| a0001c0005t0011g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| a0001c0006t0001g0001 | 0/0 | 11 | 0 | 0 | 11 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| a0001c0006t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| a0001c0006t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| a0001c0008t0001g0001 | 0/0 | 6 | 0 | 6 | 0 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| a0001c0008t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| a0001c0010t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| a0001c0010t0001g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| a0001c0010t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| a0001c0026t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| a0002c0002t0001g0001 | 0/0 | 21 | 3 | 6 | 4 | 3 | 5 | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| a0002c0002t0001g0004 | 0/0 | 17 | 1 | 3 | 11 | 0 | 2 | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| a0002c0002t0001g0008 | 0/0 | 9 | 4 | 3 | 1 | 0 | 1 | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| a0002c0002t0001g0014 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| a0002c0002t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| a0002c0002t0001g0030 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| a0002c0002t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| a0002c0002t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| a0002c0002t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| a0002c0002t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| a0002c0002t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| a0002c0002t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| a0002c0002t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| a0002c0002t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| a0002c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| a0002c0002t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| a0002c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| a0002c0002t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| a0002c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| a0002c0002t0015g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| a0002c0002t0017g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| a0002c0002t0018g0070 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| a0002c0017t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| a0002c0027t0001g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| a0003c0004t0003g0002 | 0/0 | 32 | 1 | 18 | 7 | 4 | 2 | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| a0003c0004t0003g0017 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| a0003c0004t0003g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| a0003c0004t0003g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| a0003c0004t0003g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| a0003c0004t0003g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| a0003c0004t0003g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| a0003c0004t0008g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| a0003c0004t0008g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| a0003c0004t0013g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| a0003c0004t0014g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| a0003c0004t0021g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| a0003c0014t0008g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| a0003c0015t0003g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| a0004c0007t0004g0007 | 0/0 | 6 | 3 | 3 | 0 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| a0004c0007t0007g0007 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| a0005c0009t0005g0010 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| a0005c0009t0005g0016 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| a0006c0011t0001g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| a0006c0011t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| a0007c0012t0010g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| a0008c0024t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| a0009c0018t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| a0010c0022t0007g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| a0011c0025t0005g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| a0012c0016t0020g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| a0013c0019t0002g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| a0014c0013t0003g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| a0015c0021t0019g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| a0016c0020t0002g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| a0017c0023t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0008 | c0024 | t0001 | g0023 | EUR | GBR | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG00099 | hp2 | a0002 | c0002 | t0001 | g0001 | EUR | GBR | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG00140 | hp1 | a0002 | c0002 | t0001 | g0001 | EUR | GBR | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG00140 | hp2 | a0001 | c0003 | t0002 | g0058 | EUR | GBR | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG00280 | hp2 | a0001 | c0003 | t0002 | g0043 | EUR | FIN | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG00423 | hp2 | a0001 | c0006 | t0001 | g0001 | EAS | CHS | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG00558 | hp2 | a0003 | c0015 | t0003 | g0002 | EAS | CHS | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | CHS | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG00609 | hp2 | a0003 | c0004 | t0003 | g0024 | EAS | CHS | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG00621 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | CHS | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG00639 | hp1 | a0001 | c0008 | t0001 | g0001 | AMR | PUR | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG00639 | hp2 | a0006 | c0011 | t0001 | g0008 | AMR | PUR | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG00642 | hp1 | a0001 | c0003 | t0002 | g0003 | AMR | PUR | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG00642 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG00733 | hp1 | a0002 | c0002 | t0001 | g0072 | AMR | PUR | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG00733 | hp2 | a0003 | c0004 | t0003 | g0082 | AMR | PUR | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG00735 | hp1 | a0001 | c0003 | t0002 | g0003 | AMR | PUR | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG00735 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG00738 | hp1 | a0001 | c0008 | t0001 | g0001 | AMR | PUR | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG00738 | hp2 | a0001 | c0003 | t0002 | g0003 | AMR | PUR | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG00741 | hp1 | a0002 | c0002 | t0001 | g0030 | AMR | PUR | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG00741 | hp2 | a0005 | c0009 | t0005 | g0016 | AMR | PUR | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG01069 | hp1 | a0001 | c0003 | t0002 | g0006 | AMR | PUR | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG01069 | hp2 | a0003 | c0004 | t0003 | g0002 | AMR | PUR | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG01070 | hp1 | a0002 | c0002 | t0001 | g0008 | AMR | PUR | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG01070 | hp2 | a0001 | c0003 | t0002 | g0031 | AMR | PUR | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG01071 | hp1 | a0001 | c0003 | t0002 | g0006 | AMR | PUR | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG01071 | hp2 | a0002 | c0002 | t0001 | g0008 | AMR | PUR | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG01074 | hp1 | a0002 | c0002 | t0001 | g0004 | AMR | PUR | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG01074 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG01081 | hp1 | a0001 | c0003 | t0002 | g0003 | AMR | PUR | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG01081 | hp2 | a0002 | c0002 | t0001 | g0008 | AMR | PUR | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG01099 | hp1 | a0002 | c0002 | t0001 | g0056 | AMR | PUR | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG01099 | hp2 | a0001 | c0008 | t0001 | g0001 | AMR | PUR | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG01106 | hp1 | a0004 | c0007 | t0004 | g0007 | AMR | PUR | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG01106 | hp2 | a0003 | c0004 | t0003 | g0002 | AMR | PUR | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG01109 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG01167 | hp1 | a0002 | c0002 | t0001 | g0087 | AMR | PUR | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG01167 | hp2 | a0004 | c0007 | t0004 | g0007 | AMR | PUR | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG01168 | hp1 | a0001 | c0003 | t0002 | g0003 | AMR | PUR | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG01168 | hp2 | a0002 | c0002 | t0001 | g0066 | AMR | PUR | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG01169 | hp1 | a0004 | c0007 | t0004 | g0007 | AMR | PUR | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG01169 | hp2 | a0001 | c0003 | t0002 | g0003 | AMR | PUR | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG01175 | hp1 | a0001 | c0003 | t0002 | g0006 | AMR | PUR | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG01175 | hp2 | a0003 | c0004 | t0003 | g0002 | AMR | PUR | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG01192 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG01192 | hp2 | a0001 | c0003 | t0002 | g0031 | AMR | PUR | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG01243 | hp1 | a0002 | c0002 | t0001 | g0014 | AMR | PUR | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG01243 | hp2 | a0001 | c0003 | t0002 | g0006 | AMR | PUR | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG01255 | hp1 | a0003 | c0004 | t0003 | g0002 | AMR | CLM | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG01255 | hp2 | a0001 | c0003 | t0009 | g0003 | AMR | CLM | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG01257 | hp1 | a0001 | c0003 | t0002 | g0003 | AMR | CLM | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG01257 | hp2 | a0003 | c0004 | t0008 | g0002 | AMR | CLM | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG01258 | hp1 | a0003 | c0004 | t0003 | g0002 | AMR | CLM | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG01258 | hp2 | a0001 | c0003 | t0002 | g0003 | AMR | CLM | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG01261 | hp1 | a0003 | c0004 | t0003 | g0002 | AMR | CLM | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG01261 | hp2 | a0003 | c0004 | t0003 | g0002 | AMR | CLM | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG01346 | hp1 | a0001 | c0003 | t0002 | g0009 | AMR | CLM | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG01346 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | CLM | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG01361 | hp2 | a0002 | c0002 | t0001 | g0042 | AMR | CLM | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG01433 | hp1 | a0001 | c0008 | t0001 | g0001 | AMR | CLM | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG01433 | hp2 | a0001 | c0003 | t0002 | g0003 | AMR | CLM | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG01496 | hp1 | a0001 | c0008 | t0001 | g0001 | AMR | CLM | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG01496 | hp2 | a0003 | c0004 | t0003 | g0017 | AMR | CLM | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG01515 | hp1 | a0003 | c0004 | t0003 | g0002 | EUR | IBS | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG01515 | hp2 | a0001 | c0003 | t0002 | g0003 | EUR | IBS | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG01516 | hp1 | a0002 | c0002 | t0001 | g0030 | EUR | IBS | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG01516 | hp2 | a0003 | c0004 | t0003 | g0002 | EUR | IBS | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG01517 | hp1 | a0003 | c0004 | t0003 | g0002 | EUR | IBS | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG01517 | hp2 | a0001 | c0003 | t0002 | g0003 | EUR | IBS | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG01884 | hp1 | a0001 | c0003 | t0002 | g0059 | AFR | ACB | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG01884 | hp2 | a0004 | c0007 | t0007 | g0007 | AFR | ACB | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG01891 | hp1 | a0004 | c0007 | t0007 | g0007 | AFR | ACB | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG01891 | hp2 | a0001 | c0005 | t0004 | g0005 | AFR | ACB | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG01934 | hp1 | a0003 | c0004 | t0003 | g0002 | AMR | PEL | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG01943 | hp1 | a0003 | c0004 | t0003 | g0002 | AMR | PEL | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG01943 | hp2 | a0001 | c0008 | t0001 | g0001 | AMR | PEL | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG01952 | hp1 | a0001 | c0003 | t0002 | g0003 | AMR | PEL | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG01952 | hp2 | a0003 | c0004 | t0003 | g0002 | AMR | PEL | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG01975 | hp1 | a0003 | c0004 | t0003 | g0002 | AMR | PEL | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG01975 | hp2 | a0002 | c0002 | t0001 | g0004 | AMR | PEL | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG01978 | hp2 | a0003 | c0004 | t0003 | g0002 | AMR | PEL | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG01981 | hp1 | a0001 | c0003 | t0002 | g0003 | AMR | PEL | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG01981 | hp2 | a0003 | c0004 | t0003 | g0002 | AMR | PEL | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG01993 | hp1 | a0003 | c0004 | t0003 | g0002 | AMR | PEL | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG01993 | hp2 | a0003 | c0004 | t0003 | g0002 | AMR | PEL | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG02004 | hp1 | a0003 | c0004 | t0003 | g0002 | AMR | PEL | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG02004 | hp2 | a0003 | c0004 | t0003 | g0002 | AMR | PEL | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | KHV | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG02015 | hp2 | a0003 | c0004 | t0003 | g0002 | EAS | KHV | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG02040 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | KHV | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG02055 | hp1 | a0005 | c0009 | t0005 | g0010 | AFR | ACB | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG02055 | hp2 | a0002 | c0002 | t0001 | g0023 | AFR | ACB | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG02056 | hp2 | a0002 | c0002 | t0001 | g0008 | EAS | KHV | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG02071 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | KHV | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG02080 | hp1 | a0003 | c0004 | t0013 | g0002 | EAS | KHV | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG02083 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | KHV | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG02083 | hp2 | a0009 | c0018 | t0001 | g0001 | EAS | KHV | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG02129 | hp1 | a0001 | c0006 | t0001 | g0001 | EAS | KHV | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG02129 | hp2 | a0003 | c0004 | t0003 | g0002 | EAS | KHV | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG02135 | hp1 | a0001 | c0006 | t0001 | g0001 | EAS | KHV | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG02135 | hp2 | a0003 | c0004 | t0003 | g0002 | EAS | KHV | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG02145 | hp1 | a0002 | c0002 | t0001 | g0014 | AFR | ACB | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG02145 | hp2 | a0001 | c0003 | t0002 | g0006 | AFR | ACB | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | CDX | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | CDX | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG02257 | hp1 | a0002 | c0002 | t0001 | g0008 | AFR | ACB | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG02257 | hp2 | a0001 | c0001 | t0006 | g0001 | AFR | ACB | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG02258 | hp1 | a0005 | c0009 | t0005 | g0010 | AFR | ACB | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG02258 | hp2 | a0001 | c0001 | t0004 | g0028 | AFR | ACB | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG02293 | hp1 | a0003 | c0004 | t0003 | g0002 | AMR | PEL | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG02293 | hp2 | a0001 | c0008 | t0001 | g0088 | AMR | PEL | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG02300 | hp1 | a0002 | c0002 | t0001 | g0004 | AMR | PEL | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG02300 | hp2 | a0001 | c0003 | t0002 | g0009 | AMR | PEL | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG02451 | hp1 | a0001 | c0003 | t0004 | g0047 | AFR | ACB | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG02451 | hp2 | a0001 | c0001 | t0004 | g0054 | AFR | ACB | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG02572 | hp1 | a0001 | c0003 | t0004 | g0041 | AFR | GWD | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG02572 | hp2 | a0001 | c0003 | t0002 | g0006 | AFR | GWD | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG02615 | hp1 | a0004 | c0007 | t0004 | g0007 | AFR | GWD | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG02615 | hp2 | a0001 | c0003 | t0004 | g0036 | AFR | GWD | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG02630 | hp1 | a0002 | c0002 | t0001 | g0008 | AFR | GWD | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG02630 | hp2 | a0001 | c0001 | t0004 | g0049 | AFR | GWD | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG02647 | hp1 | a0002 | c0002 | t0001 | g0001 | AFR | GWD | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG02647 | hp2 | a0002 | c0002 | t0001 | g0008 | AFR | GWD | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG02683 | hp1 | a0001 | c0003 | t0009 | g0003 | SAS | PJL | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG02683 | hp2 | a0002 | c0002 | t0001 | g0001 | SAS | PJL | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG02698 | hp1 | a0011 | c0025 | t0005 | g0016 | SAS | PJL | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG02717 | hp1 | a0012 | c0016 | t0020 | g0040 | AFR | GWD | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG02717 | hp2 | a0001 | c0005 | t0004 | g0005 | AFR | GWD | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG02723 | hp1 | a0001 | c0005 | t0004 | g0005 | AFR | GWD | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG02723 | hp2 | a0001 | c0005 | t0004 | g0038 | AFR | GWD | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG02735 | hp1 | a0001 | c0003 | t0002 | g0003 | SAS | PJL | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG02735 | hp2 | a0001 | c0003 | t0002 | g0003 | SAS | PJL | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0083 | SAS | PJL | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG02809 | hp1 | a0005 | c0009 | t0005 | g0010 | AFR | GWD | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG02809 | hp2 | a0002 | c0002 | t0001 | g0014 | AFR | GWD | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG02818 | hp1 | a0001 | c0005 | t0004 | g0005 | AFR | GWD | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG02886 | hp1 | a0001 | c0005 | t0004 | g0005 | AFR | GWD | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG02886 | hp2 | a0001 | c0003 | t0002 | g0006 | AFR | GWD | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG02895 | hp1 | a0004 | c0007 | t0004 | g0007 | AFR | GWD | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG02895 | hp2 | a0001 | c0003 | t0002 | g0006 | AFR | GWD | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG02896 | hp1 | a0001 | c0001 | t0004 | g0048 | AFR | GWD | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG02896 | hp2 | a0001 | c0003 | t0002 | g0006 | AFR | GWD | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG02922 | hp1 | a0001 | c0003 | t0002 | g0019 | AFR | ESN | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG02922 | hp2 | a0007 | c0012 | t0010 | g0026 | AFR | ESN | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG02965 | hp1 | a0001 | c0003 | t0002 | g0063 | AFR | ESN | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG02965 | hp2 | a0001 | c0001 | t0004 | g0051 | AFR | ESN | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | ESN | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG02970 | hp2 | a0002 | c0002 | t0001 | g0008 | AFR | ESN | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG02976 | hp1 | a0001 | c0003 | t0002 | g0006 | AFR | ESN | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG02976 | hp2 | a0001 | c0001 | t0004 | g0011 | AFR | ESN | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG03041 | hp1 | a0001 | c0003 | t0002 | g0006 | AFR | GWD | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG03041 | hp2 | a0013 | c0019 | t0002 | g0019 | AFR | GWD | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG03098 | hp1 | a0002 | c0002 | t0001 | g0001 | AFR | MSL | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG03098 | hp2 | a0002 | c0002 | t0001 | g0032 | AFR | MSL | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG03130 | hp1 | a0002 | c0002 | t0001 | g0032 | AFR | ESN | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG03130 | hp2 | a0001 | c0001 | t0004 | g0028 | AFR | ESN | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG03139 | hp1 | a0001 | c0005 | t0004 | g0005 | AFR | ESN | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG03139 | hp2 | a0002 | c0002 | t0001 | g0080 | AFR | ESN | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG03195 | hp1 | a0004 | c0007 | t0007 | g0007 | AFR | ESN | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG03195 | hp2 | a0001 | c0005 | t0011 | g0005 | AFR | ESN | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG03209 | hp1 | a0002 | c0002 | t0001 | g0071 | AFR | MSL | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG03209 | hp2 | a0001 | c0005 | t0004 | g0005 | AFR | MSL | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG03225 | hp1 | a0004 | c0007 | t0004 | g0007 | AFR | MSL | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG03225 | hp2 | a0001 | c0005 | t0004 | g0005 | AFR | MSL | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG03239 | hp1 | a0002 | c0002 | t0001 | g0078 | SAS | PJL | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0073 | SAS | PJL | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG03453 | hp1 | a0005 | c0009 | t0005 | g0010 | AFR | MSL | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG03453 | hp2 | a0001 | c0005 | t0004 | g0005 | AFR | MSL | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG03486 | hp1 | a0001 | c0001 | t0004 | g0052 | AFR | MSL | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG03490 | hp2 | a0001 | c0003 | t0002 | g0021 | SAS | PJL | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG03516 | hp1 | a0001 | c0005 | t0004 | g0005 | AFR | ESN | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG03516 | hp2 | a0001 | c0003 | t0002 | g0060 | AFR | ESN | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG03540 | hp1 | a0001 | c0003 | t0004 | g0035 | AFR | GWD | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG03540 | hp2 | a0001 | c0001 | t0004 | g0050 | AFR | GWD | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG03579 | hp1 | a0002 | c0002 | t0001 | g0001 | AFR | MSL | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG03579 | hp2 | a0005 | c0009 | t0005 | g0016 | AFR | MSL | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG03654 | hp1 | a0001 | c0003 | t0002 | g0003 | SAS | PJL | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG03654 | hp2 | a0001 | c0003 | t0002 | g0021 | SAS | PJL | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG03669 | hp1 | a0002 | c0002 | t0001 | g0001 | SAS | PJL | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG03688 | hp2 | a0002 | c0002 | t0001 | g0004 | SAS | STU | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG03704 | hp1 | a0002 | c0002 | t0001 | g0089 | SAS | PJL | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG03704 | hp2 | a0002 | c0027 | t0001 | g0001 | SAS | PJL | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG03831 | hp1 | a0002 | c0002 | t0017 | g0001 | SAS | BEB | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG03831 | hp2 | a0002 | c0002 | t0001 | g0001 | SAS | BEB | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG03834 | hp1 | a0003 | c0004 | t0003 | g0002 | SAS | BEB | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG03927 | hp1 | a0014 | c0013 | t0003 | g0044 | SAS | BEB | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG03927 | hp2 | a0002 | c0002 | t0001 | g0001 | SAS | BEB | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG04115 | hp1 | a0001 | c0003 | t0002 | g0003 | SAS | STU | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG04115 | hp2 | a0001 | c0003 | t0002 | g0062 | SAS | STU | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG04184 | hp1 | a0003 | c0004 | t0003 | g0002 | SAS | BEB | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG04184 | hp2 | a0001 | c0003 | t0016 | g0009 | SAS | BEB | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG04199 | hp1 | a0001 | c0003 | t0003 | g0079 | SAS | STU | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG04199 | hp2 | a0002 | c0002 | t0001 | g0001 | SAS | STU | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0015 | SAS | STU | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG04204 | hp2 | a0002 | c0002 | t0001 | g0008 | SAS | STU | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0013 | SAS | STU | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | YRI | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| NA18522 | hp2 | a0001 | c0001 | t0004 | g0011 | AFR | YRI | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| NA18747 | hp1 | a0001 | c0006 | t0001 | g0077 | EAS | CHB | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| NA18906 | hp1 | a0002 | c0002 | t0001 | g0061 | AFR | YRI | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| NA18906 | hp2 | a0001 | c0003 | t0002 | g0019 | AFR | YRI | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| NA18942 | hp1 | a0003 | c0004 | t0003 | g0018 | EAS | JPT | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| NA18943 | hp1 | a0001 | c0006 | t0001 | g0001 | EAS | JPT | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| NA18943 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| NA18945 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| NA18946 | hp1 | a0003 | c0004 | t0008 | g0053 | EAS | JPT | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| NA18951 | hp1 | a0001 | c0006 | t0001 | g0001 | EAS | JPT | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| NA18951 | hp2 | a0001 | c0003 | t0002 | g0057 | EAS | JPT | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| NA18953 | hp1 | a0003 | c0004 | t0003 | g0017 | EAS | JPT | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| NA18956 | hp1 | a0001 | c0010 | t0001 | g0067 | EAS | JPT | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| NA18956 | hp2 | a0002 | c0002 | t0001 | g0033 | EAS | JPT | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| NA18957 | hp1 | a0001 | c0006 | t0001 | g0001 | EAS | JPT | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| NA18957 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| NA18959 | hp1 | a0003 | c0004 | t0003 | g0002 | EAS | JPT | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| NA18960 | hp1 | a0001 | c0006 | t0001 | g0081 | EAS | JPT | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| NA18961 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| NA18962 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| NA18963 | hp1 | a0003 | c0004 | t0003 | g0025 | EAS | JPT | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| NA18967 | hp1 | a0002 | c0017 | t0001 | g0085 | EAS | JPT | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| NA18971 | hp2 | a0001 | c0003 | t0002 | g0009 | EAS | JPT | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| NA18973 | hp2 | a0003 | c0004 | t0003 | g0025 | EAS | JPT | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| NA18975 | hp2 | a0001 | c0006 | t0001 | g0001 | EAS | JPT | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| NA18977 | hp2 | a0001 | c0001 | t0012 | g0001 | EAS | JPT | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| NA18980 | hp2 | a0001 | c0006 | t0001 | g0001 | EAS | JPT | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| NA18983 | hp1 | a0001 | c0010 | t0001 | g0001 | EAS | JPT | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| NA18984 | hp1 | a0003 | c0004 | t0003 | g0002 | EAS | JPT | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| NA18985 | hp1 | a0003 | c0004 | t0014 | g0002 | EAS | JPT | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| NA18986 | hp2 | a0001 | c0010 | t0001 | g0012 | EAS | JPT | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| NA18990 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| NA18994 | hp1 | a0001 | c0010 | t0001 | g0012 | EAS | JPT | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| NA18997 | hp1 | a0001 | c0010 | t0001 | g0012 | EAS | JPT | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| NA18997 | hp2 | a0001 | c0001 | t0006 | g0001 | EAS | JPT | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| NA18998 | hp1 | a0001 | c0006 | t0001 | g0001 | EAS | JPT | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| NA19000 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| NA19003 | hp2 | a0003 | c0004 | t0003 | g0029 | EAS | JPT | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| NA19005 | hp2 | a0001 | c0006 | t0001 | g0001 | EAS | JPT | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| NA19009 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| NA19009 | hp2 | a0001 | c0010 | t0001 | g0012 | EAS | JPT | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| NA19010 | hp1 | a0001 | c0001 | t0006 | g0001 | EAS | JPT | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | LWK | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| NA19030 | hp2 | a0001 | c0001 | t0004 | g0055 | AFR | LWK | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| NA19043 | hp1 | a0015 | c0021 | t0019 | g0039 | AFR | LWK | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| NA19043 | hp2 | a0002 | c0002 | t0001 | g0014 | AFR | LWK | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| NA19054 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| NA19057 | hp1 | a0003 | c0004 | t0003 | g0018 | EAS | JPT | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| NA19057 | hp2 | a0003 | c0004 | t0003 | g0017 | EAS | JPT | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| NA19058 | hp2 | a0001 | c0006 | t0001 | g0001 | EAS | JPT | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| NA19060 | hp1 | a0001 | c0001 | t0006 | g0001 | EAS | JPT | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| NA19060 | hp2 | a0002 | c0002 | t0001 | g0084 | EAS | JPT | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| NA19063 | hp1 | a0003 | c0004 | t0003 | g0002 | EAS | JPT | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| NA19065 | hp1 | a0003 | c0014 | t0008 | g0002 | EAS | JPT | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| NA19067 | hp1 | a0001 | c0003 | t0002 | g0009 | EAS | JPT | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| NA19067 | hp2 | a0001 | c0001 | t0006 | g0001 | EAS | JPT | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| NA19068 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| NA19068 | hp2 | a0016 | c0020 | t0002 | g0009 | EAS | JPT | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| NA19074 | hp2 | a0001 | c0003 | t0002 | g0009 | EAS | JPT | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| NA19077 | hp2 | a0002 | c0002 | t0001 | g0033 | EAS | JPT | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| NA19081 | hp1 | a0003 | c0004 | t0003 | g0002 | EAS | JPT | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| NA19082 | hp1 | a0017 | c0023 | t0001 | g0076 | EAS | JPT | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| NA19082 | hp2 | a0003 | c0004 | t0003 | g0029 | EAS | JPT | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| NA19084 | hp1 | a0003 | c0004 | t0003 | g0024 | EAS | JPT | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| NA19084 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| NA19085 | hp1 | a0001 | c0026 | t0001 | g0001 | EAS | JPT | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| NA19085 | hp2 | a0003 | c0004 | t0003 | g0018 | EAS | JPT | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| NA20129 | hp1 | a0001 | c0005 | t0004 | g0005 | AFR | ASW | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| NA20129 | hp2 | a0003 | c0004 | t0003 | g0002 | AFR | ASW | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| NA20752 | hp1 | a0003 | c0004 | t0003 | g0002 | EUR | TSI | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| NA20752 | hp2 | a0001 | c0003 | t0002 | g0003 | EUR | TSI | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| NA20805 | hp1 | a0002 | c0002 | t0001 | g0001 | EUR | TSI | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| NA20805 | hp2 | a0001 | c0003 | t0002 | g0064 | EUR | TSI | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| NA20905 | hp1 | a0001 | c0003 | t0002 | g0021 | SAS | GIH | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| NA20905 | hp2 | a0002 | c0002 | t0001 | g0004 | SAS | GIH | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG01123 | hp1 | a0003 | c0004 | t0021 | g0002 | AMR | CLM | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG01123 | hp2 | a0006 | c0011 | t0001 | g0086 | AMR | CLM | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG02109 | hp1 | a0001 | c0005 | t0004 | g0037 | AFR | ACB | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG02486 | hp1 | a0001 | c0005 | t0004 | g0005 | AFR | ACB | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG02486 | hp2 | a0007 | c0012 | t0010 | g0026 | AFR | ACB | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG02559 | hp1 | a0010 | c0022 | t0007 | g0007 | AFR | ACB | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG02559 | hp2 | a0001 | c0005 | t0011 | g0005 | AFR | ACB | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG03471 | hp1 | a0001 | c0003 | t0002 | g0006 | AFR | MSL | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG03471 | hp2 | a0001 | c0005 | t0004 | g0005 | AFR | MSL | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG06807 | hp1 | a0001 | c0001 | t0004 | g0011 | AFR | USA | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| HG06807 | hp2 | a0001 | c0001 | t0004 | g0027 | AFR | USA | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| NA20300 | hp1 | a0002 | c0002 | t0001 | g0004 | AFR | USA | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| NA20300 | hp2 | a0001 | c0005 | t0004 | g0005 | AFR | USA | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| NA21309 | hp1 | a0002 | c0002 | t0015 | g0001 | AFR | LWK | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| NA21309 | hp2 | a0001 | c0001 | t0004 | g0027 | AFR | LWK | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| homoSapiens | chm13v2 | a0002 | c0002 | t0018 | g0070 | REF | REF | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0004 | g0011 | REF | REF | XYLT2_chr17_50341126_50366185 | XYLT2 | chr17 | 50341126 | 50366185 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:50353660 | G | A | 1 | a0006 | 2 | HG00639.hp2 HG01123.hp2 |
missense_variant | MODERATE | c.166G>A | p.Asp56Asn | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 2/11 | 181/3507 | 166/2598 | 56/865 | chr17 | 50353660 | |||
| chr17:50353784 | G | A | 1 | a0012 | 1 | HG02717.hp1 | missense_variant | MODERATE | c.290G>A | p.Arg97Gln | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 2/11 | 305/3507 | 290/2598 | 97/865 | chr17 | 50353784 | |||
| chr17:50354439 | G | C | 1 | a0014 | 1 | HG03927.hp1 | missense_variant | MODERATE | c.660G>C | p.Glu220Asp | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 3/11 | 675/3507 | 660/2598 | 220/865 | chr17 | 50354439 | |||
| chr17:50354963 | G | C | 2 | a0003 a0014 |
53 | HG00558.hp2 HG00609.hp2 HG00733.hp2 others(50): Show |
missense_variant | MODERATE | c.914G>C | p.Arg305Thr | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 4/11 | 929/3507 | 914/2598 | 305/865 | chr17 | 50354963 | |||
| chr17:50355945 | C | T | 2 | a0005 a0011 |
7 | HG00741.hp2 HG02055.hp1 HG02258.hp1 others(4): Show |
missense_variant | MODERATE | c.1253C>T | p.Pro418Leu | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 6/11 | 1268/3507 | 1253/2598 | 418/865 | chr17 | 50355945 | |||
| chr17:50356229 | G | A | 1 | a0009 | 1 | HG02083.hp2 | missense_variant | MODERATE | c.1450G>A | p.Asp484Asn | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 7/11 | 1465/3507 | 1450/2598 | 484/865 | chr17 | 50356229 | |||
| chr17:50356647 | C | T | 2 | a0012 a0015 |
2 | HG02717.hp1 NA19043.hp1 |
missense_variant | MODERATE | c.1619C>T | p.Thr540Ile | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 8/11 | 1634/3507 | 1619/2598 | 540/865 | chr17 | 50356647 | |||
| chr17:50357156 | G | C | 2 | a0004 a0010 |
10 | HG01106.hp1 HG01167.hp2 HG01169.hp1 others(7): Show |
missense_variant | MODERATE | c.1845G>C | p.Gln615His | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 9/11 | 1860/3507 | 1845/2598 | 615/865 | chr17 | 50357156 | |||
| chr17:50357218 | G | A | 2 | a0010 a0013 |
2 | HG02559.hp1 HG03041.hp2 |
missense_variant | MODERATE | c.1907G>A | p.Arg636His | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 9/11 | 1922/3507 | 1907/2598 | 636/865 | chr17 | 50357218 | |||
| chr17:50358288 | G | A | 1 | a0007 | 2 | HG02486.hp2 HG02922.hp2 |
missense_variant | MODERATE | c.2023G>A | p.Val675Met | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 10/11 | 2038/3507 | 2023/2598 | 675/865 | chr17 | 50358288 | |||
| chr17:50358423 | C | T | 1 | a0016 | 1 | NA19068.hp2 | missense_variant | MODERATE | c.2158C>T | p.Arg720Trp | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 10/11 | 2173/3507 | 2158/2598 | 720/865 | chr17 | 50358423 | |||
| chr17:50358517 | A | G | 1 | a0011 | 1 | HG02698.hp1 | missense_variant | MODERATE | c.2252A>G | p.Asn751Ser | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 10/11 | 2267/3507 | 2252/2598 | 751/865 | chr17 | 50358517 | |||
| chr17:50360038 | G | C | 1 | a0017 | 1 | NA19082.hp1 | missense_variant | MODERATE | c.2345G>C | p.Ser782Thr | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 11/11 | 2360/3507 | 2345/2598 | 782/865 | chr17 | 50360038 | |||
| chr17:50360095 | C | G | 3 | a0002 a0006 a0008 |
76 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(73): Show |
missense_variant | MODERATE | c.2402C>G | p.Thr801Arg | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 11/11 | 2417/3507 | 2402/2598 | 801/865 | chr17 | 50360095 | |||
| chr17:50360220 | A | G | 1 | a0008 | 1 | HG00099.hp1 | missense_variant | MODERATE | c.2527A>G | p.Ser843Gly | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 11/11 | 2542/3507 | 2527/2598 | 843/865 | chr17 | 50360220 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:50346170 | G | T | 1 | a0001c0005 | 18 | HG01891.hp2 HG02109.hp1 HG02486.hp1 others(15): Show |
synonymous_variant | LOW | c.30G>T | p.Leu10Leu | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 1/11 | 45/3507 | 30/2598 | 10/865 | chr17 | 50346170 | |||
| chr17:50353671 | G | A | 4 | a0003c0004 a0003c0014 a0003c0015 others(1): Show |
53 | HG00558.hp2 HG00609.hp2 HG00733.hp2 others(50): Show |
synonymous_variant | LOW | c.177G>A | p.Glu59Glu | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 2/11 | 192/3507 | 177/2598 | 59/865 | chr17 | 50353671 | |||
| chr17:50353836 | C | T | 4 | a0003c0004 a0003c0014 a0003c0015 others(1): Show |
53 | HG00558.hp2 HG00609.hp2 HG00733.hp2 others(50): Show |
synonymous_variant | LOW | c.342C>T | p.Pro114Pro | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 2/11 | 357/3507 | 342/2598 | 114/865 | chr17 | 50353836 | |||
| chr17:50354859 | C | T | 1 | a0001c0010 | 6 | NA18956.hp1 NA18983.hp1 NA18986.hp2 others(3): Show |
synonymous_variant | LOW | c.810C>T | p.Ser270Ser | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 4/11 | 825/3507 | 810/2598 | 270/865 | chr17 | 50354859 | |||
| chr17:50354907 | C | T | 1 | a0002c0027 | 1 | HG03704.hp2 | synonymous_variant | LOW | c.858C>T | p.Asn286Asn | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 4/11 | 873/3507 | 858/2598 | 286/865 | chr17 | 50354907 | |||
| chr17:50354919 | G | A | 1 | a0002c0017 | 1 | NA18967.hp1 | synonymous_variant | LOW | c.870G>A | p.Thr290Thr | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 4/11 | 885/3507 | 870/2598 | 290/865 | chr17 | 50354919 | |||
| chr17:50354971 | C | T | 1 | a0001c0008 | 7 | HG00639.hp1 HG00738.hp1 HG01099.hp2 others(4): Show |
synonymous_variant | LOW | c.922C>T | p.Leu308Leu | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 4/11 | 937/3507 | 922/2598 | 308/865 | chr17 | 50354971 | |||
| chr17:50355847 | C | T | 1 | a0001c0026 | 1 | NA19085.hp1 | synonymous_variant | LOW | c.1155C>T | p.Gly385Gly | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 6/11 | 1170/3507 | 1155/2598 | 385/865 | chr17 | 50355847 | |||
| chr17:50356597 | T | C | 13 | a0001c0003 a0001c0005 a0003c0004 others(10): Show |
142 | HG00140.hp2 HG00280.hp2 HG00558.hp2 others(139): Show |
synonymous_variant | LOW | c.1569T>C | p.Tyr523Tyr | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 8/11 | 1584/3507 | 1569/2598 | 523/865 | chr17 | 50356597 | |||
| chr17:50357249 | G | A | 1 | a0001c0006 | 13 | HG00423.hp2 HG02129.hp1 HG02135.hp1 others(10): Show |
synonymous_variant | LOW | c.1938G>A | p.Leu646Leu | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 9/11 | 1953/3507 | 1938/2598 | 646/865 | chr17 | 50357249 | |||
| chr17:50358389 | G | A | 1 | a0003c0014 | 1 | NA19065.hp1 | synonymous_variant | LOW | c.2124G>A | p.Glu708Glu | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 10/11 | 2139/3507 | 2124/2598 | 708/865 | chr17 | 50358389 | |||
| chr17:50358423 | C | A | 1 | a0003c0015 | 1 | HG00558.hp2 | synonymous_variant | LOW | c.2158C>A | p.Arg720Arg | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 10/11 | 2173/3507 | 2158/2598 | 720/865 | chr17 | 50358423 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:50360344 | A | G | 1 | a0003c0004t0021 | 1 | HG01123.hp1 | 3_prime_UTR_variant | MODIFIER | c.*53A>G | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 11/11 | 53 | chr17 | 50360344 | ||||||
| chr17:50360498 | C | T | 2 | a0012c0016t0020 a0015c0021t0019 |
2 | HG02717.hp1 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*207C>T | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 11/11 | 207 | chr17 | 50360498 | ||||||
| chr17:50360499 | G | A | 1 | a0001c0003t0009 | 2 | HG01255.hp2 HG02683.hp1 |
3_prime_UTR_variant | MODIFIER | c.*208G>A | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 11/11 | 208 | chr17 | 50360499 | ||||||
| chr17:50360569 | T | C | 1 | a0007c0012t0010 | 2 | HG02486.hp2 HG02922.hp2 |
3_prime_UTR_variant | MODIFIER | c.*278T>C | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 11/11 | 278 | chr17 | 50360569 | ||||||
| chr17:50360571 | C | CT | 18 | a0001c0001t0001 a0001c0001t0004 a0001c0003t0004 others(15): Show |
198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
3_prime_UTR_variant | MODIFIER | c.*299dupT | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 11/11 | 300 | INFO_REALIGN_3_PRIME | chr17 | 50360571 | |||||
| chr17:50360571 | C | CTTTT | 1 | a0001c0003t0002 | 17 | HG00140.hp2 HG01069.hp1 HG01070.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*296_*299dupTTTT | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 11/11 | 300 | INFO_REALIGN_3_PRIME | chr17 | 50360571 | |||||
| chr17:50360571 | C | CTTTTT | 5 | a0001c0003t0002 a0001c0003t0009 a0001c0003t0016 others(2): Show |
38 | HG00280.hp2 HG00642.hp1 HG00735.hp1 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*295_*299dupTTTTT | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 11/11 | 300 | INFO_REALIGN_3_PRIME | chr17 | 50360571 | |||||
| chr17:50360571 | CTT | C | 2 | a0005c0009t0005 a0011c0025t0005 |
7 | HG00741.hp2 HG02055.hp1 HG02258.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*298_*299delTT | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 11/11 | 298 | INFO_REALIGN_3_PRIME | chr17 | 50360571 | |||||
| chr17:50360574 | T | TC | 1 | a0001c0001t0006 | 5 | HG02257.hp2 NA18997.hp2 NA19010.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*283_*284insC | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 11/11 | 284 | chr17 | 50360574 | ||||||
| chr17:50360575 | T | C | 1 | a0001c0001t0012 | 1 | NA18977.hp2 | 3_prime_UTR_variant | MODIFIER | c.*284T>C | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 11/11 | 284 | chr17 | 50360575 | ||||||
| chr17:50360576 | T | TC | 7 | a0001c0003t0003 a0003c0004t0003 a0003c0004t0013 others(4): Show |
51 | HG00558.hp2 HG00609.hp2 HG00733.hp2 others(48): Show |
3_prime_UTR_variant | MODIFIER | c.*285_*286insC | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 11/11 | 286 | chr17 | 50360576 | ||||||
| chr17:50360577 | T | C | 2 | a0003c0004t0008 a0003c0014t0008 |
3 | HG01257.hp2 NA18946.hp1 NA19065.hp1 |
3_prime_UTR_variant | MODIFIER | c.*286T>C | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 11/11 | 286 | chr17 | 50360577 | ||||||
| chr17:50360607 | T | C | 1 | a0001c0005t0011 | 2 | HG02559.hp2 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*316T>C | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 11/11 | 316 | chr17 | 50360607 | ||||||
| chr17:50360620 | G | A | 1 | a0002c0002t0015 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*329G>A | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 11/11 | 329 | chr17 | 50360620 | ||||||
| chr17:50360622 | G | A | 2 | a0004c0007t0007 a0010c0022t0007 |
4 | HG01884.hp2 HG01891.hp1 HG02559.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*331G>A | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 11/11 | 331 | chr17 | 50360622 | ||||||
| chr17:50360694 | G | T | 16 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0012 others(13): Show |
192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
3_prime_UTR_variant | MODIFIER | c.*403G>T | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 11/11 | 403 | chr17 | 50360694 | ||||||
| chr17:50360727 | C | T | 1 | a0001c0003t0016 | 1 | HG04184.hp2 | 3_prime_UTR_variant | MODIFIER | c.*436C>T | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 11/11 | 436 | chr17 | 50360727 | ||||||
| chr17:50360787 | G | A | 7 | a0001c0003t0002 a0001c0003t0009 a0001c0003t0016 others(4): Show |
57 | HG00140.hp2 HG00280.hp2 HG00642.hp1 others(54): Show |
3_prime_UTR_variant | MODIFIER | c.*496G>A | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 11/11 | 496 | chr17 | 50360787 | ||||||
| chr17:50360860 | G | A | 2 | a0005c0009t0005 a0011c0025t0005 |
7 | HG00741.hp2 HG02055.hp1 HG02258.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*569G>A | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 11/11 | 569 | chr17 | 50360860 | ||||||
| chr17:50360926 | C | T | 1 | a0002c0002t0017 | 1 | HG03831.hp1 | 3_prime_UTR_variant | MODIFIER | c.*635C>T | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 11/11 | 635 | chr17 | 50360926 | ||||||
| chr17:50360946 | A | G | 1 | a0012c0016t0020 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*655A>G | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 11/11 | 655 | chr17 | 50360946 | ||||||
| chr17:50361025 | G | A | 1 | a0003c0004t0013 | 1 | HG02080.hp1 | 3_prime_UTR_variant | MODIFIER | c.*734G>A | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 11/11 | 734 | chr17 | 50361025 | ||||||
| chr17:50361143 | A | C | 1 | a0003c0004t0014 | 1 | NA18985.hp1 | 3_prime_UTR_variant | MODIFIER | c.*852A>C | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 11/11 | 852 | chr17 | 50361143 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:50346298 | G | A | 1 | a0001c0001t0001g0034 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.135+23G>A | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 1/10 | chr17 | 50346298 | |||||||
| chr17:50346373 | G | C | 11 | a0001c0003t0004g0035 a0001c0003t0004g0036 a0001c0005t0004g0005 others(8): Show |
29 | HG00741.hp2 HG01891.hp2 HG02055.hp1 others(26): Show |
intron_variant | MODIFIER | c.135+98G>C | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 1/10 | chr17 | 50346373 | |||||||
| chr17:50346385 | C | T | 1 | a0001c0001t0001g0092 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.135+110C>T | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 1/10 | chr17 | 50346385 | |||||||
| chr17:50346539 | A | G | 11 | a0001c0003t0004g0035 a0001c0003t0004g0036 a0001c0005t0004g0005 others(8): Show |
29 | HG00741.hp2 HG01891.hp2 HG02055.hp1 others(26): Show |
intron_variant | MODIFIER | c.135+264A>G | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 1/10 | chr17 | 50346539 | |||||||
| chr17:50346594 | G | T | 52 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0015 others(49): Show |
188 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.135+319G>T | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 1/10 | chr17 | 50346594 | |||||||
| chr17:50347103 | G | T | 11 | a0001c0003t0004g0035 a0001c0003t0004g0036 a0001c0005t0004g0005 others(8): Show |
29 | HG00741.hp2 HG01891.hp2 HG02055.hp1 others(26): Show |
intron_variant | MODIFIER | c.135+828G>T | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 1/10 | chr17 | 50347103 | |||||||
| chr17:50347117 | C | T | 21 | a0001c0001t0004g0054 a0001c0001t0004g0055 a0001c0003t0002g0003 others(18): Show |
57 | HG00140.hp2 HG00642.hp1 HG00735.hp1 others(54): Show |
intron_variant | MODIFIER | c.135+842C>T | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 1/10 | chr17 | 50347117 | |||||||
| chr17:50347123 | C | T | 1 | a0001c0001t0001g0091 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.135+848C>T | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 1/10 | chr17 | 50347123 | |||||||
| chr17:50347239 | C | G | 2 | a0003c0004t0003g0029 a0003c0004t0008g0053 |
3 | NA18946.hp1 NA19003.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.135+964C>G | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 1/10 | chr17 | 50347239 | |||||||
| chr17:50347275 | ACT | A | 5 | a0001c0003t0004g0035 a0001c0003t0004g0036 a0005c0009t0005g0010 others(2): Show |
9 | HG00741.hp2 HG02055.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.135+1003_135+1004d others(4): Show |
XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 50347275 | ||||||
| chr17:50347296 | C | G | 11 | a0001c0003t0004g0035 a0001c0003t0004g0036 a0001c0005t0004g0005 others(8): Show |
29 | HG00741.hp2 HG01891.hp2 HG02055.hp1 others(26): Show |
intron_variant | MODIFIER | c.135+1021C>G | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 1/10 | chr17 | 50347296 | |||||||
| chr17:50347297 | G | C | 2 | a0001c0001t0004g0054 a0001c0001t0004g0055 |
2 | HG02451.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.135+1022G>C | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 1/10 | chr17 | 50347297 | |||||||
| chr17:50347453 | A | C | 1 | a0001c0003t0002g0064 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.135+1178A>C | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 1/10 | chr17 | 50347453 | |||||||
| chr17:50347583 | A | G | 63 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0015 others(60): Show |
208 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(205): Show |
intron_variant | MODIFIER | c.135+1308A>G | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 1/10 | chr17 | 50347583 | |||||||
| chr17:50347698 | G | A | 1 | a0001c0001t0001g0065 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.135+1423G>A | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 1/10 | chr17 | 50347698 | |||||||
| chr17:50347833 | T | G | 6 | a0001c0003t0004g0035 a0001c0003t0004g0041 a0001c0005t0004g0005 others(3): Show |
20 | HG01891.hp2 HG02109.hp1 HG02486.hp1 others(17): Show |
intron_variant | MODIFIER | c.135+1558T>G | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 1/10 | chr17 | 50347833 | |||||||
| chr17:50347975 | T | G | 10 | a0001c0001t0004g0027 a0001c0001t0004g0048 a0001c0001t0004g0049 others(7): Show |
25 | HG01891.hp2 HG02109.hp1 HG02486.hp1 others(22): Show |
intron_variant | MODIFIER | c.135+1700T>G | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 1/10 | chr17 | 50347975 | |||||||
| chr17:50348023 | C | G | 4 | a0001c0003t0004g0036 a0005c0009t0005g0010 a0005c0009t0005g0016 others(1): Show |
8 | HG00741.hp2 HG02055.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.135+1748C>G | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 1/10 | chr17 | 50348023 | |||||||
| chr17:50348063 | A | C | 4 | a0001c0001t0004g0027 a0001c0001t0004g0048 a0001c0001t0004g0049 others(1): Show |
5 | HG02630.hp2 HG02896.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.135+1788A>C | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 1/10 | chr17 | 50348063 | |||||||
| chr17:50348064 | A | T | 6 | a0001c0003t0004g0036 a0005c0009t0005g0010 a0005c0009t0005g0016 others(3): Show |
10 | HG00741.hp2 HG02055.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.135+1789A>T | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 1/10 | chr17 | 50348064 | |||||||
| chr17:50348099 | G | GATTC | 23 | a0001c0003t0002g0043 a0001c0005t0004g0005 a0001c0005t0004g0037 others(20): Show |
75 | HG00099.hp1 HG00280.hp2 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.135+1845_135+1848d others(6): Show |
XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 50348099 | ||||||
| chr17:50348145 | A | G | 4 | a0001c0001t0004g0027 a0001c0001t0004g0048 a0001c0001t0004g0049 others(1): Show |
5 | HG02630.hp2 HG02896.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.135+1870A>G | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 1/10 | chr17 | 50348145 | |||||||
| chr17:50348149 | T | C | 1 | a0002c0002t0001g0032 | 2 | HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.135+1874T>C | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 1/10 | chr17 | 50348149 | |||||||
| chr17:50348337 | G | C | 2 | a0001c0010t0001g0012 a0001c0010t0001g0067 |
5 | NA18956.hp1 NA18986.hp2 NA18994.hp1 others(2): Show |
intron_variant | MODIFIER | c.135+2062G>C | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 1/10 | chr17 | 50348337 | |||||||
| chr17:50348592 | C | A | 1 | a0001c0001t0001g0092 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.135+2317C>A | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 1/10 | chr17 | 50348592 | |||||||
| chr17:50348606 | T | G | 74 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0015 others(71): Show |
237 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.135+2331T>G | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 1/10 | chr17 | 50348606 | |||||||
| chr17:50348620 | C | G | 1 | a0001c0001t0001g0090 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.135+2345C>G | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 1/10 | chr17 | 50348620 | |||||||
| chr17:50348788 | G | C | 4 | a0001c0003t0004g0036 a0005c0009t0005g0010 a0005c0009t0005g0016 others(1): Show |
8 | HG00741.hp2 HG02055.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.135+2513G>C | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 1/10 | chr17 | 50348788 | |||||||
| chr17:50348812 | C | T | 2 | a0001c0001t0004g0054 a0001c0001t0004g0055 |
2 | HG02451.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.135+2537C>T | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 1/10 | chr17 | 50348812 | |||||||
| chr17:50348854 | C | T | 1 | a0001c0003t0004g0047 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.135+2579C>T | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 1/10 | chr17 | 50348854 | |||||||
| chr17:50348902 | CTG | C | 5 | a0001c0001t0001g0013 a0001c0001t0001g0068 a0001c0001t0001g0069 others(2): Show |
11 | HG00609.hp1 HG03017.hp2 HG04228.hp2 others(8): Show |
intron_variant | MODIFIER | c.135+2630_135+2631d others(4): Show |
XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 50348902 | ||||||
| chr17:50348998 | C | A | 4 | a0001c0003t0004g0036 a0005c0009t0005g0010 a0005c0009t0005g0016 others(1): Show |
8 | HG00741.hp2 HG02055.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.135+2723C>A | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 1/10 | chr17 | 50348998 | |||||||
| chr17:50349070 | T | G | 1 | a0007c0012t0010g0026 | 2 | HG02486.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.135+2795T>G | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 1/10 | chr17 | 50349070 | |||||||
| chr17:50349108 | C | T | 1 | a0001c0001t0001g0015 | 4 | HG02698.hp2 HG03017.hp1 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.135+2833C>T | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 1/10 | chr17 | 50349108 | |||||||
| chr17:50349212 | C | T | 1 | a0002c0002t0001g0089 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.135+2937C>T | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 1/10 | chr17 | 50349212 | |||||||
| chr17:50349400 | G | T | 3 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0003t0004g0035 |
3 | HG02970.hp1 HG03540.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.135+3125G>T | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 1/10 | chr17 | 50349400 | |||||||
| chr17:50349427 | C | T | 19 | a0001c0003t0002g0003 a0001c0003t0002g0006 a0001c0003t0002g0009 others(16): Show |
55 | HG00140.hp2 HG00642.hp1 HG00735.hp1 others(52): Show |
intron_variant | MODIFIER | c.135+3152C>T | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 1/10 | chr17 | 50349427 | |||||||
| chr17:50349470 | C | T | 1 | a0001c0003t0002g0062 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.135+3195C>T | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 1/10 | chr17 | 50349470 | |||||||
| chr17:50349558 | G | A | 21 | a0001c0003t0002g0003 a0001c0003t0002g0006 a0001c0003t0002g0009 others(18): Show |
57 | HG00140.hp2 HG00642.hp1 HG00735.hp1 others(54): Show |
intron_variant | MODIFIER | c.135+3283G>A | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 1/10 | chr17 | 50349558 | |||||||
| chr17:50349607 | C | T | 1 | a0001c0008t0001g0088 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.135+3332C>T | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 1/10 | chr17 | 50349607 | |||||||
| chr17:50349608 | A | G | 4 | a0001c0003t0004g0036 a0005c0009t0005g0010 a0005c0009t0005g0016 others(1): Show |
8 | HG00741.hp2 HG02055.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.135+3333A>G | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 1/10 | chr17 | 50349608 | |||||||
| chr17:50349632 | C | T | 3 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0003t0004g0035 |
3 | HG02970.hp1 HG03540.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.135+3357C>T | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 1/10 | chr17 | 50349632 | |||||||
| chr17:50349644 | A | C | 18 | a0001c0003t0002g0043 a0002c0002t0001g0023 a0002c0002t0001g0042 others(15): Show |
56 | HG00099.hp1 HG00280.hp2 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.135+3369A>C | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 1/10 | chr17 | 50349644 | |||||||
| chr17:50349796 | C | A | 1 | a0015c0021t0019g0039 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.135+3521C>A | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 1/10 | chr17 | 50349796 | |||||||
| chr17:50349830 | C | T | 62 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0015 others(59): Show |
207 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.135+3555C>T | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 1/10 | chr17 | 50349830 | |||||||
| chr17:50349945 | G | C | 52 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0015 others(49): Show |
188 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.135+3670G>C | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 1/10 | chr17 | 50349945 | |||||||
| chr17:50349954 | G | A | 4 | a0001c0001t0004g0051 a0004c0007t0004g0007 a0004c0007t0007g0007 others(1): Show |
11 | HG01106.hp1 HG01167.hp2 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.136-3676G>A | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 1/10 | chr17 | 50349954 | |||||||
| chr17:50349958 | AGATCACT others(376): Show |
A | 4 | a0002c0002t0001g0008 a0002c0002t0001g0087 a0006c0011t0001g0008 others(1): Show |
12 | HG00639.hp2 HG01070.hp1 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.136-3653_136-3271d others(2): Show |
XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 50349958 | ||||||
| chr17:50350028 | C | T | 20 | a0001c0003t0002g0003 a0001c0003t0002g0006 a0001c0003t0002g0009 others(17): Show |
56 | HG00140.hp2 HG00642.hp1 HG00735.hp1 others(53): Show |
intron_variant | MODIFIER | c.136-3602C>T | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 1/10 | chr17 | 50350028 | |||||||
| chr17:50350097 | C | G | 4 | a0001c0003t0004g0036 a0005c0009t0005g0010 a0005c0009t0005g0016 others(1): Show |
8 | HG00741.hp2 HG02055.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.136-3533C>G | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 1/10 | chr17 | 50350097 | |||||||
| chr17:50350142 | TACTGCAC others(377): Show |
T | 57 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0015 others(54): Show |
194 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.136-3468_136-3085d others(2): Show |
XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 50350142 | ||||||
| chr17:50350164 | CAGAGTGA others(377): Show |
C | 1 | a0002c0027t0001g0001 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.136-3452_136-3069d others(2): Show |
XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 50350164 | ||||||
| chr17:50350182 | CA | C | 32 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0003t0002g0003 others(29): Show |
96 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.136-3423delA | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 50350182 | ||||||
| chr17:50350182 | CAA | C | 5 | a0001c0003t0002g0006 a0001c0005t0004g0005 a0002c0002t0001g0056 others(2): Show |
6 | HG01099.hp1 HG01943.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.136-3424_136-3423d others(4): Show |
XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 50350182 | ||||||
| chr17:50350182 | CAAA | C | 6 | a0001c0003t0004g0041 a0001c0005t0004g0005 a0001c0005t0004g0037 others(3): Show |
18 | HG01891.hp2 HG02055.hp1 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.136-3425_136-3423d others(5): Show |
XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 50350182 | ||||||
| chr17:50350182 | CAAAA | C | 4 | a0001c0003t0004g0036 a0005c0009t0005g0010 a0005c0009t0005g0016 others(1): Show |
7 | HG00741.hp2 HG02258.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.136-3426_136-3423d others(6): Show |
XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 50350182 | ||||||
| chr17:50350291 | C | G | 2 | a0001c0001t0004g0054 a0001c0001t0004g0055 |
2 | HG02451.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.136-3339C>G | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 1/10 | chr17 | 50350291 | |||||||
| chr17:50350621 | C | G | 9 | a0001c0003t0002g0019 a0002c0002t0001g0008 a0002c0002t0001g0087 others(6): Show |
22 | HG00639.hp2 HG00741.hp2 HG01070.hp1 others(19): Show |
intron_variant | MODIFIER | c.136-3009C>G | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 1/10 | chr17 | 50350621 | |||||||
| chr17:50350657 | G | T | 1 | a0015c0021t0019g0039 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.136-2973G>T | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 1/10 | chr17 | 50350657 | |||||||
| chr17:50350744 | C | T | 5 | a0002c0002t0001g0004 a0002c0002t0001g0033 a0002c0002t0001g0084 others(2): Show |
22 | HG01074.hp1 HG01975.hp2 HG02040.hp2 others(19): Show |
intron_variant | MODIFIER | c.136-2886C>T | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 1/10 | chr17 | 50350744 | |||||||
| chr17:50350799 | GGT | G | 13 | a0001c0001t0004g0048 a0001c0003t0004g0036 a0001c0003t0004g0041 others(10): Show |
34 | HG01106.hp1 HG01167.hp2 HG01169.hp1 others(31): Show |
intron_variant | MODIFIER | c.136-2829_136-2828d others(4): Show |
XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 50350799 | ||||||
| chr17:50350958 | A | G | 113 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0015 others(110): Show |
350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.136-2672A>G | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 1/10 | chr17 | 50350958 | |||||||
| chr17:50350962 | C | T | 1 | a0001c0001t0001g0022 | 3 | HG02109.hp2 HG02818.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.136-2668C>T | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 1/10 | chr17 | 50350962 | |||||||
| chr17:50350974 | G | A | 1 | a0002c0002t0001g0084 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.136-2656G>A | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 1/10 | chr17 | 50350974 | |||||||
| chr17:50351104 | C | T | 1 | a0001c0001t0001g0083 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.136-2526C>T | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 1/10 | chr17 | 50351104 | |||||||
| chr17:50351236 | T | C | 3 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0003t0004g0035 |
3 | HG02970.hp1 HG03540.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.136-2394T>C | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 1/10 | chr17 | 50351236 | |||||||
| chr17:50351245 | A | G | 1 | a0001c0001t0004g0052 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.136-2385A>G | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 1/10 | chr17 | 50351245 | |||||||
| chr17:50351262 | G | C | 101 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0015 others(98): Show |
302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.136-2368G>C | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 1/10 | chr17 | 50351262 | |||||||
| chr17:50351638 | A | G | 1 | a0001c0006t0001g0081 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.136-1992A>G | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 1/10 | chr17 | 50351638 | |||||||
| chr17:50351857 | G | A | 1 | a0002c0002t0001g0072 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.136-1773G>A | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 1/10 | chr17 | 50351857 | |||||||
| chr17:50351918 | G | A | 3 | a0001c0001t0004g0027 a0001c0001t0004g0049 a0001c0001t0004g0050 |
4 | HG02630.hp2 HG03540.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.136-1712G>A | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 1/10 | chr17 | 50351918 | |||||||
| chr17:50352084 | C | T | 3 | a0002c0002t0001g0014 a0002c0002t0001g0061 a0002c0002t0001g0071 |
6 | HG01243.hp1 HG02145.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.136-1546C>T | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 1/10 | chr17 | 50352084 | |||||||
| chr17:50352319 | G | T | 1 | a0002c0002t0001g0080 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.136-1311G>T | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 1/10 | chr17 | 50352319 | |||||||
| chr17:50352321 | G | A | 6 | a0001c0003t0004g0036 a0001c0003t0004g0041 a0001c0005t0004g0005 others(3): Show |
20 | HG01891.hp2 HG02109.hp1 HG02486.hp1 others(17): Show |
intron_variant | MODIFIER | c.136-1309G>A | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 1/10 | chr17 | 50352321 | |||||||
| chr17:50352335 | C | T | 6 | a0001c0003t0004g0036 a0001c0003t0004g0041 a0001c0005t0004g0005 others(3): Show |
20 | HG01891.hp2 HG02109.hp1 HG02486.hp1 others(17): Show |
intron_variant | MODIFIER | c.136-1295C>T | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 1/10 | chr17 | 50352335 | |||||||
| chr17:50352377 | C | T | 3 | a0005c0009t0005g0010 a0005c0009t0005g0016 a0011c0025t0005g0016 |
7 | HG00741.hp2 HG02055.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.136-1253C>T | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 1/10 | chr17 | 50352377 | |||||||
| chr17:50352400 | G | A | 1 | a0001c0003t0002g0057 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.136-1230G>A | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 1/10 | chr17 | 50352400 | |||||||
| chr17:50352479 | C | G | 2 | a0001c0003t0004g0035 a0007c0012t0010g0026 |
3 | HG02486.hp2 HG02922.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.136-1151C>G | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 1/10 | chr17 | 50352479 | |||||||
| chr17:50352485 | C | T | 3 | a0005c0009t0005g0010 a0005c0009t0005g0016 a0011c0025t0005g0016 |
7 | HG00741.hp2 HG02055.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.136-1145C>T | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 1/10 | chr17 | 50352485 | |||||||
| chr17:50352504 | A | G | 20 | a0001c0001t0004g0050 a0001c0003t0002g0003 a0001c0003t0002g0006 others(17): Show |
57 | HG00140.hp2 HG00280.hp2 HG00642.hp1 others(54): Show |
intron_variant | MODIFIER | c.136-1126A>G | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 1/10 | chr17 | 50352504 | |||||||
| chr17:50352550 | G | A | 1 | a0001c0003t0004g0041 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.136-1080G>A | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 1/10 | chr17 | 50352550 | |||||||
| chr17:50352571 | A | G | 48 | a0001c0001t0004g0050 a0001c0003t0002g0003 a0001c0003t0002g0006 others(45): Show |
142 | HG00140.hp2 HG00280.hp2 HG00558.hp2 others(139): Show |
intron_variant | MODIFIER | c.136-1059A>G | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 1/10 | chr17 | 50352571 | |||||||
| chr17:50352622 | C | A | 1 | a0001c0001t0001g0073 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.136-1008C>A | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 1/10 | chr17 | 50352622 | |||||||
| chr17:50352700 | C | T | 3 | a0005c0009t0005g0010 a0005c0009t0005g0016 a0011c0025t0005g0016 |
7 | HG00741.hp2 HG02055.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.136-930C>T | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 1/10 | chr17 | 50352700 | |||||||
| chr17:50352836 | A | G | 2 | a0001c0001t0001g0020 a0001c0001t0001g0083 |
4 | HG02738.hp1 HG02738.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.136-794A>G | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 1/10 | chr17 | 50352836 | |||||||
| chr17:50352930 | C | T | 39 | a0001c0001t0004g0050 a0001c0003t0002g0003 a0001c0003t0002g0006 others(36): Show |
115 | HG00140.hp2 HG00280.hp2 HG00558.hp2 others(112): Show |
intron_variant | MODIFIER | c.136-700C>T | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 1/10 | chr17 | 50352930 | |||||||
| chr17:50352960 | G | A | 6 | a0001c0003t0004g0036 a0001c0003t0004g0041 a0001c0005t0004g0005 others(3): Show |
20 | HG01891.hp2 HG02109.hp1 HG02486.hp1 others(17): Show |
intron_variant | MODIFIER | c.136-670G>A | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 1/10 | chr17 | 50352960 | |||||||
| chr17:50352970 | C | T | 3 | a0005c0009t0005g0010 a0005c0009t0005g0016 a0011c0025t0005g0016 |
7 | HG00741.hp2 HG02055.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.136-660C>T | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 1/10 | chr17 | 50352970 | |||||||
| chr17:50353022 | C | T | 3 | a0005c0009t0005g0010 a0005c0009t0005g0016 a0011c0025t0005g0016 |
7 | HG00741.hp2 HG02055.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.136-608C>T | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 1/10 | chr17 | 50353022 | |||||||
| chr17:50353023 | G | A | 1 | a0001c0001t0001g0074 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.136-607G>A | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 1/10 | chr17 | 50353023 | |||||||
| chr17:50353158 | C | G | 1 | a0001c0001t0004g0055 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.136-472C>G | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 1/10 | chr17 | 50353158 | |||||||
| chr17:50353173 | T | C | 3 | a0005c0009t0005g0010 a0005c0009t0005g0016 a0011c0025t0005g0016 |
7 | HG00741.hp2 HG02055.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.136-457T>C | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 1/10 | chr17 | 50353173 | |||||||
| chr17:50353287 | C | A | 3 | a0005c0009t0005g0010 a0005c0009t0005g0016 a0011c0025t0005g0016 |
7 | HG00741.hp2 HG02055.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.136-343C>A | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 1/10 | chr17 | 50353287 | |||||||
| chr17:50353301 | G | A | 1 | a0001c0001t0001g0045 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.136-329G>A | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 1/10 | chr17 | 50353301 | |||||||
| chr17:50353333 | G | A | 48 | a0001c0001t0004g0050 a0001c0003t0002g0003 a0001c0003t0002g0006 others(45): Show |
142 | HG00140.hp2 HG00280.hp2 HG00558.hp2 others(139): Show |
intron_variant | MODIFIER | c.136-297G>A | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 1/10 | chr17 | 50353333 | |||||||
| chr17:50353401 | C | T | 1 | a0001c0003t0004g0047 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.136-229C>T | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 1/10 | chr17 | 50353401 | |||||||
| chr17:50353467 | A | G | 3 | a0005c0009t0005g0010 a0005c0009t0005g0016 a0011c0025t0005g0016 |
7 | HG00741.hp2 HG02055.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.136-163A>G | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 1/10 | chr17 | 50353467 | |||||||
| chr17:50353603 | A | C | 6 | a0001c0003t0004g0036 a0001c0003t0004g0041 a0001c0005t0004g0005 others(3): Show |
20 | HG01891.hp2 HG02109.hp1 HG02486.hp1 others(17): Show |
intron_variant | MODIFIER | c.136-27A>C | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 1/10 | chr17 | 50353603 | |||||||
| chr17:50354292 | C | A | 1 | a0012c0016t0020g0040 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.629-116C>A | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 2/10 | chr17 | 50354292 | |||||||
| chr17:50354364 | G | T | 1 | a0002c0002t0001g0042 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.629-44G>T | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 2/10 | chr17 | 50354364 | |||||||
| chr17:50354681 | G | GA | 115 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0015 others(112): Show |
353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.804+98_804+99insA | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 3/10 | chr17 | 50354681 | |||||||
| chr17:50354709 | A | G | 9 | a0001c0003t0004g0036 a0001c0003t0004g0041 a0001c0005t0004g0005 others(6): Show |
27 | HG00741.hp2 HG01891.hp2 HG02055.hp1 others(24): Show |
intron_variant | MODIFIER | c.804+126A>G | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 3/10 | chr17 | 50354709 | |||||||
| chr17:50355164 | G | T | 1 | a0014c0013t0003g0044 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1007+108G>T | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 4/10 | chr17 | 50355164 | |||||||
| chr17:50355308 | C | G | 1 | a0001c0005t0004g0038 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1008-193C>G | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 4/10 | chr17 | 50355308 | |||||||
| chr17:50355320 | G | A | 62 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0015 others(59): Show |
198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
intron_variant | MODIFIER | c.1008-181G>A | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 4/10 | chr17 | 50355320 | |||||||
| chr17:50355388 | G | C | 23 | a0001c0003t0002g0003 a0001c0003t0002g0006 a0001c0003t0002g0009 others(20): Show |
74 | HG00140.hp2 HG00280.hp2 HG00642.hp1 others(71): Show |
intron_variant | MODIFIER | c.1008-113G>C | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 4/10 | chr17 | 50355388 | |||||||
| chr17:50355663 | C | T | 1 | a0002c0002t0001g0033 | 2 | NA18956.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.1088+82C>T | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 5/10 | chr17 | 50355663 | |||||||
| chr17:50355720 | G | A | 47 | a0001c0003t0002g0003 a0001c0003t0002g0006 a0001c0003t0002g0009 others(44): Show |
141 | HG00140.hp2 HG00280.hp2 HG00558.hp2 others(138): Show |
intron_variant | MODIFIER | c.1089-61G>A | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 5/10 | chr17 | 50355720 | |||||||
| chr17:50356026 | G | C | 5 | a0001c0003t0004g0036 a0001c0005t0004g0005 a0001c0005t0004g0037 others(2): Show |
19 | HG01891.hp2 HG02109.hp1 HG02486.hp1 others(16): Show |
intron_variant | MODIFIER | c.1305+29G>C | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 6/10 | chr17 | 50356026 | |||||||
| chr17:50356342 | A | C | 9 | a0001c0003t0004g0036 a0001c0003t0004g0041 a0001c0005t0004g0005 others(6): Show |
27 | HG00741.hp2 HG01891.hp2 HG02055.hp1 others(24): Show |
intron_variant | MODIFIER | c.1482+81A>C | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 7/10 | chr17 | 50356342 | |||||||
| chr17:50356413 | C | T | 4 | a0001c0005t0004g0005 a0001c0005t0004g0037 a0001c0005t0004g0038 others(1): Show |
18 | HG01891.hp2 HG02109.hp1 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.1483-98C>T | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 7/10 | chr17 | 50356413 | |||||||
| chr17:50357020 | C | T | 1 | a0001c0001t0004g0055 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1746-37C>T | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 8/10 | chr17 | 50357020 | |||||||
| chr17:50357319 | G | A | 6 | a0001c0003t0004g0036 a0001c0003t0004g0041 a0001c0005t0004g0005 others(3): Show |
20 | HG01891.hp2 HG02109.hp1 HG02486.hp1 others(17): Show |
intron_variant | MODIFIER | c.1941+67G>A | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 9/10 | chr17 | 50357319 | |||||||
| chr17:50357342 | G | A | 1 | a0002c0002t0001g0084 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1941+90G>A | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 9/10 | chr17 | 50357342 | |||||||
| chr17:50357378 | C | T | 4 | a0001c0005t0004g0005 a0001c0005t0004g0037 a0001c0005t0004g0038 others(1): Show |
18 | HG01891.hp2 HG02109.hp1 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.1941+126C>T | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 9/10 | chr17 | 50357378 | |||||||
| chr17:50357504 | A | G | 1 | a0002c0002t0001g0087 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1941+252A>G | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 9/10 | chr17 | 50357504 | |||||||
| chr17:50357592 | C | CT | 26 | a0001c0001t0001g0069 a0001c0001t0001g0092 a0001c0001t0004g0050 others(23): Show |
47 | HG01069.hp1 HG01070.hp2 HG01071.hp1 others(44): Show |
intron_variant | MODIFIER | c.1941+357dupT | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr17 | 50357592 | ||||||
| chr17:50357592 | C | CTT | 5 | a0001c0003t0002g0060 a0001c0003t0004g0041 a0001c0005t0004g0005 others(2): Show |
19 | HG01891.hp2 HG02486.hp1 HG02559.hp2 others(16): Show |
intron_variant | MODIFIER | c.1941+356_1941+357d others(4): Show |
XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr17 | 50357592 | ||||||
| chr17:50357679 | G | A | 1 | a0001c0001t0001g0075 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1941+427G>A | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 9/10 | chr17 | 50357679 | |||||||
| chr17:50357700 | C | T | 2 | a0002c0002t0001g0072 a0002c0002t0001g0078 |
2 | HG00733.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.1941+448C>T | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 9/10 | chr17 | 50357700 | |||||||
| chr17:50357763 | A | G | 9 | a0001c0003t0004g0036 a0001c0003t0004g0041 a0001c0005t0004g0005 others(6): Show |
27 | HG00741.hp2 HG01891.hp2 HG02055.hp1 others(24): Show |
intron_variant | MODIFIER | c.1942-444A>G | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 9/10 | chr17 | 50357763 | |||||||
| chr17:50357770 | C | T | 1 | a0001c0003t0004g0035 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1942-437C>T | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 9/10 | chr17 | 50357770 | |||||||
| chr17:50357797 | A | G | 9 | a0001c0003t0004g0036 a0001c0003t0004g0041 a0001c0005t0004g0005 others(6): Show |
27 | HG00741.hp2 HG01891.hp2 HG02055.hp1 others(24): Show |
intron_variant | MODIFIER | c.1942-410A>G | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 9/10 | chr17 | 50357797 | |||||||
| chr17:50357859 | C | T | 1 | a0001c0001t0004g0049 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1942-348C>T | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 9/10 | chr17 | 50357859 | |||||||
| chr17:50357868 | C | T | 1 | a0001c0003t0002g0058 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1942-339C>T | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 9/10 | chr17 | 50357868 | |||||||
| chr17:50357960 | C | T | 4 | a0001c0001t0004g0027 a0001c0001t0004g0048 a0001c0001t0004g0049 others(1): Show |
5 | HG02630.hp2 HG02896.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.1942-247C>T | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 9/10 | chr17 | 50357960 | |||||||
| chr17:50358074 | A | G | 1 | a0001c0003t0002g0059 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1942-133A>G | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 9/10 | chr17 | 50358074 | |||||||
| chr17:50358090 | A | C | 6 | a0001c0003t0004g0036 a0001c0003t0004g0041 a0001c0005t0004g0005 others(3): Show |
20 | HG01891.hp2 HG02109.hp1 HG02486.hp1 others(17): Show |
intron_variant | MODIFIER | c.1942-117A>C | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 9/10 | chr17 | 50358090 | |||||||
| chr17:50358579 | C | G | 1 | a0001c0003t0004g0036 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2275+39C>G | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 10/10 | chr17 | 50358579 | |||||||
| chr17:50358591 | C | T | 1 | a0001c0003t0004g0047 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2275+51C>T | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 10/10 | chr17 | 50358591 | |||||||
| chr17:50358645 | A | C | 2 | a0001c0001t0001g0068 a0001c0001t0001g0069 |
2 | NA18967.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.2275+105A>C | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 10/10 | chr17 | 50358645 | |||||||
| chr17:50358677 | ATCT | A | 1 | a0003c0004t0003g0018 | 3 | NA18942.hp1 NA19057.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.2275+142_2275+144d others(5): Show |
XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr17 | 50358677 | ||||||
| chr17:50358693 | C | A | 1 | a0001c0001t0001g0091 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.2275+153C>A | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 10/10 | chr17 | 50358693 | |||||||
| chr17:50358809 | C | A | 1 | a0001c0003t0004g0035 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2275+269C>A | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 10/10 | chr17 | 50358809 | |||||||
| chr17:50359050 | G | A | 1 | a0002c0002t0001g0056 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.2275+510G>A | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 10/10 | chr17 | 50359050 | |||||||
| chr17:50359145 | A | G | 1 | a0003c0004t0003g0017 | 3 | HG01496.hp2 NA18953.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.2275+605A>G | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 10/10 | chr17 | 50359145 | |||||||
| chr17:50359152 | T | A | 1 | a0001c0003t0004g0036 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2275+612T>A | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 10/10 | chr17 | 50359152 | |||||||
| chr17:50359186 | C | T | 6 | a0001c0003t0002g0009 a0001c0003t0002g0031 a0001c0003t0002g0057 others(3): Show |
11 | HG01070.hp2 HG01192.hp2 HG01346.hp1 others(8): Show |
intron_variant | MODIFIER | c.2275+646C>T | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 10/10 | chr17 | 50359186 | |||||||
| chr17:50359230 | C | T | 1 | a0002c0002t0001g0080 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2275+690C>T | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 10/10 | chr17 | 50359230 | |||||||
| chr17:50359339 | C | T | 1 | a0001c0006t0001g0077 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.2276-630C>T | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 10/10 | chr17 | 50359339 | |||||||
| chr17:50359438 | G | A | 1 | a0012c0016t0020g0040 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2276-531G>A | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 10/10 | chr17 | 50359438 | |||||||
| chr17:50359501 | C | A | 1 | a0017c0023t0001g0076 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.2276-468C>A | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 10/10 | chr17 | 50359501 | |||||||
| chr17:50359546 | G | C | 1 | a0001c0003t0002g0031 | 2 | HG01070.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.2276-423G>C | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 10/10 | chr17 | 50359546 | |||||||
| chr17:50359763 | G | A | 1 | a0003c0004t0003g0025 | 2 | NA18963.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.2276-206G>A | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 10/10 | chr17 | 50359763 | |||||||
| chr17:50359932 | G | A | 4 | a0001c0005t0004g0005 a0001c0005t0004g0037 a0001c0005t0004g0038 others(1): Show |
18 | HG01891.hp2 HG02109.hp1 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.2276-37G>A | XYLT2 | ENSG00000015532.10 | transcript | ENST00000017003.7 | protein_coding | 10/10 | chr17 | 50359932 |