Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 2813 |
| ensemblid | ENSG00000169347.17 |
| hgncid | 4441 |
| symbol | GP2 |
| name | glycoprotein 2 |
| refseq_nuc | NM_001502.4 |
| refseq_prot | NP_001493.2 |
| ensembl_nuc | ENST00000302555.10 |
| ensembl_prot | ENSP00000304044.6 |
| mane_status | MANE Select |
| chr | chr16 |
| start | 20309574 |
| end | 20327513 |
| strand | - |
| ver | v1.2 |
| region | chr16:20309574-20327513 |
| region5000 | chr16:20304574-20332513 |
| regionname0 | GP2_chr16_20309574_20327513 |
| regionname5000 | GP2_chr16_20304574_20332513 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 534 | 367 | 88 | 77 | 140 | 17 | 43 | 105 | GP2_chr16_20304574_20332513 | GP2 | MPHLM others(529): Show |
chr16 | 20304574 | 20332513 |
| a0002 | 0/0 | 534 | 18 | 0 | 0 | 15 | 0 | 3 | 13 | GP2_chr16_20304574_20332513 | GP2 | MPHLM others(529): Show |
chr16 | 20304574 | 20332513 |
| a0003 | 0/0 | 534 | 2 | 0 | 0 | 2 | 0 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | MPHLM others(529): Show |
chr16 | 20304574 | 20332513 |
| a0004 | 0/0 | 534 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GP2_chr16_20304574_20332513 | GP2 | MPHLM others(529): Show |
chr16 | 20304574 | 20332513 |
| a0005 | 0/0 | 534 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | MPHLM others(529): Show |
chr16 | 20304574 | 20332513 |
| a0006 | 0/0 | 534 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | MPHLM others(529): Show |
chr16 | 20304574 | 20332513 |
| a0007 | 0/0 | 534 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GP2_chr16_20304574_20332513 | GP2 | MPHLM others(529): Show |
chr16 | 20304574 | 20332513 |
| a0008 | 0/0 | 534 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | MPHLM others(529): Show |
chr16 | 20304574 | 20332513 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1605 | 256 | 52 | 50 | 120 | 5 | 27 | GP2_chr16_20304574_20332513 | GP2 | ATGCC others(1600): Show |
chr16 | 20304574 | 20332513 | ||
| a0001c0002 | 0/0 | 1605 | 55 | 5 | 10 | 20 | 7 | 13 | GP2_chr16_20304574_20332513 | GP2 | ATGCC others(1600): Show |
chr16 | 20304574 | 20332513 | ||
| a0001c0003 | 0/0 | 1605 | 20 | 2 | 11 | 0 | 5 | 2 | GP2_chr16_20304574_20332513 | GP2 | ATGCC others(1600): Show |
chr16 | 20304574 | 20332513 | ||
| a0001c0005 | 0/0 | 1605 | 16 | 14 | 2 | 0 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | ATGCC others(1600): Show |
chr16 | 20304574 | 20332513 | ||
| a0001c0006 | 0/0 | 1605 | 6 | 5 | 1 | 0 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | ATGCC others(1600): Show |
chr16 | 20304574 | 20332513 | ||
| a0001c0007 | 0/0 | 1605 | 6 | 6 | 0 | 0 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | ATGCC others(1600): Show |
chr16 | 20304574 | 20332513 | ||
| a0001c0009 | 0/0 | 1605 | 2 | 1 | 1 | 0 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | ATGCC others(1600): Show |
chr16 | 20304574 | 20332513 | ||
| a0001c0010 | 0/0 | 1605 | 1 | 0 | 0 | 0 | 0 | 1 | GP2_chr16_20304574_20332513 | GP2 | ATGCC others(1600): Show |
chr16 | 20304574 | 20332513 | ||
| a0001c0011 | 0/0 | 1605 | 1 | 1 | 0 | 0 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | ATGCC others(1600): Show |
chr16 | 20304574 | 20332513 | ||
| a0001c0014 | 0/0 | 1605 | 1 | 1 | 0 | 0 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | ATGCC others(1600): Show |
chr16 | 20304574 | 20332513 | ||
| a0001c0015 | 0/0 | 1605 | 1 | 0 | 1 | 0 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | ATGCC others(1600): Show |
chr16 | 20304574 | 20332513 | ||
| a0001c0019 | 0/0 | 1605 | 1 | 0 | 1 | 0 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | ATGCC others(1600): Show |
chr16 | 20304574 | 20332513 | ||
| a0001c0020 | 0/0 | 1605 | 1 | 1 | 0 | 0 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | ATGCC others(1600): Show |
chr16 | 20304574 | 20332513 | ||
| a0002c0004 | 0/0 | 1605 | 18 | 0 | 0 | 15 | 0 | 3 | GP2_chr16_20304574_20332513 | GP2 | ATGCC others(1600): Show |
chr16 | 20304574 | 20332513 | ||
| a0003c0008 | 0/0 | 1605 | 2 | 0 | 0 | 2 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | ATGCC others(1600): Show |
chr16 | 20304574 | 20332513 | ||
| a0004c0012 | 0/0 | 1605 | 1 | 0 | 0 | 1 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | ATGCC others(1600): Show |
chr16 | 20304574 | 20332513 | ||
| a0005c0017 | 0/0 | 1605 | 1 | 0 | 0 | 0 | 1 | 0 | GP2_chr16_20304574_20332513 | GP2 | ATGCC others(1600): Show |
chr16 | 20304574 | 20332513 | ||
| a0006c0016 | 0/0 | 1605 | 1 | 0 | 0 | 1 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | ATGCC others(1600): Show |
chr16 | 20304574 | 20332513 | ||
| a0007c0018 | 0/0 | 1605 | 1 | 0 | 0 | 1 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | ATGCC others(1600): Show |
chr16 | 20304574 | 20332513 | ||
| a0008c0013 | 0/0 | 1605 | 1 | 0 | 1 | 0 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | ATGCC others(1600): Show |
chr16 | 20304574 | 20332513 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3339 | 98 | 0 | 10 | 76 | 0 | 12 | GP2_chr16_20304574_20332513 | GP2 | ATTCC others(3334): Show |
chr16 | 20304574 | 20332513 |
| a0001c0001t0002 | 0/0 | 3338 | 2 | 1 | 0 | 0 | 0 | 1 | GP2_chr16_20304574_20332513 | GP2 | ATTCC others(3333): Show |
chr16 | 20304574 | 20332513 |
| a0001c0001t0003 | 0/1 | 3337 | 73 | 33 | 22 | 5 | 5 | 7 | GP2_chr16_20304574_20332513 | GP2 | ATTCC others(3332): Show |
chr16 | 20304574 | 20332513 |
| a0001c0001t0004 | 1/0 | 3337 | 48 | 1 | 13 | 31 | 0 | 2 | GP2_chr16_20304574_20332513 | GP2 | ATTCC others(3332): Show |
chr16 | 20304574 | 20332513 |
| a0001c0001t0005 | 0/0 | 3337 | 2 | 0 | 0 | 0 | 0 | 2 | GP2_chr16_20304574_20332513 | GP2 | ATTCC others(3332): Show |
chr16 | 20304574 | 20332513 |
| a0001c0001t0006 | 0/0 | 3343 | 1 | 1 | 0 | 0 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | ATTCC others(3338): Show |
chr16 | 20304574 | 20332513 |
| a0001c0001t0007 | 0/0 | 3343 | 1 | 1 | 0 | 0 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | ATTCC others(3338): Show |
chr16 | 20304574 | 20332513 |
| a0001c0001t0008 | 0/0 | 3337 | 8 | 5 | 2 | 0 | 0 | 1 | GP2_chr16_20304574_20332513 | GP2 | ATTCC others(3332): Show |
chr16 | 20304574 | 20332513 |
| a0001c0001t0009 | 0/0 | 3337 | 7 | 7 | 0 | 0 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | ATTCC others(3332): Show |
chr16 | 20304574 | 20332513 |
| a0001c0001t0010 | 0/0 | 3337 | 5 | 0 | 2 | 3 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | ATTCC others(3332): Show |
chr16 | 20304574 | 20332513 |
| a0001c0001t0011 | 0/0 | 3337 | 3 | 0 | 0 | 2 | 0 | 1 | GP2_chr16_20304574_20332513 | GP2 | ATTCC others(3332): Show |
chr16 | 20304574 | 20332513 |
| a0001c0001t0013 | 0/0 | 3337 | 1 | 1 | 0 | 0 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | ATTCC others(3332): Show |
chr16 | 20304574 | 20332513 |
| a0001c0001t0014 | 0/0 | 3338 | 2 | 0 | 0 | 2 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | ATTCC others(3333): Show |
chr16 | 20304574 | 20332513 |
| a0001c0001t0017 | 0/0 | 3339 | 1 | 1 | 0 | 0 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | ATTCC others(3334): Show |
chr16 | 20304574 | 20332513 |
| a0001c0001t0019 | 0/0 | 3338 | 1 | 0 | 0 | 0 | 0 | 1 | GP2_chr16_20304574_20332513 | GP2 | ATTCC others(3333): Show |
chr16 | 20304574 | 20332513 |
| a0001c0001t0021 | 0/0 | 3337 | 1 | 0 | 0 | 1 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | ATTCC others(3332): Show |
chr16 | 20304574 | 20332513 |
| a0001c0001t0022 | 0/0 | 3343 | 1 | 1 | 0 | 0 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | ATTCC others(3338): Show |
chr16 | 20304574 | 20332513 |
| a0001c0001t0024 | 0/0 | 3337 | 1 | 0 | 1 | 0 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | ATTCC others(3332): Show |
chr16 | 20304574 | 20332513 |
| a0001c0002t0002 | 0/0 | 3338 | 44 | 0 | 8 | 18 | 5 | 13 | GP2_chr16_20304574_20332513 | GP2 | ATTCC others(3333): Show |
chr16 | 20304574 | 20332513 |
| a0001c0002t0003 | 0/0 | 3337 | 2 | 0 | 0 | 2 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | ATTCC others(3332): Show |
chr16 | 20304574 | 20332513 |
| a0001c0002t0005 | 0/0 | 3337 | 8 | 4 | 2 | 0 | 2 | 0 | GP2_chr16_20304574_20332513 | GP2 | ATTCC others(3332): Show |
chr16 | 20304574 | 20332513 |
| a0001c0002t0018 | 0/0 | 3338 | 1 | 1 | 0 | 0 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | ATTCC others(3333): Show |
chr16 | 20304574 | 20332513 |
| a0001c0003t0002 | 0/0 | 3338 | 20 | 2 | 11 | 0 | 5 | 2 | GP2_chr16_20304574_20332513 | GP2 | ATTCC others(3333): Show |
chr16 | 20304574 | 20332513 |
| a0001c0005t0002 | 0/0 | 3338 | 2 | 2 | 0 | 0 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | ATTCC others(3333): Show |
chr16 | 20304574 | 20332513 |
| a0001c0005t0006 | 0/0 | 3343 | 6 | 6 | 0 | 0 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | ATTCC others(3338): Show |
chr16 | 20304574 | 20332513 |
| a0001c0005t0007 | 0/0 | 3343 | 8 | 6 | 2 | 0 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | ATTCC others(3338): Show |
chr16 | 20304574 | 20332513 |
| a0001c0006t0006 | 0/0 | 3343 | 3 | 3 | 0 | 0 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | ATTCC others(3338): Show |
chr16 | 20304574 | 20332513 |
| a0001c0006t0012 | 0/0 | 3343 | 3 | 2 | 1 | 0 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | ATTCC others(3338): Show |
chr16 | 20304574 | 20332513 |
| a0001c0007t0002 | 0/0 | 3338 | 5 | 5 | 0 | 0 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | ATTCC others(3333): Show |
chr16 | 20304574 | 20332513 |
| a0001c0007t0003 | 0/0 | 3337 | 1 | 1 | 0 | 0 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | ATTCC others(3332): Show |
chr16 | 20304574 | 20332513 |
| a0001c0009t0005 | 0/0 | 3337 | 2 | 1 | 1 | 0 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | ATTCC others(3332): Show |
chr16 | 20304574 | 20332513 |
| a0001c0010t0003 | 0/0 | 3337 | 1 | 0 | 0 | 0 | 0 | 1 | GP2_chr16_20304574_20332513 | GP2 | ATTCC others(3332): Show |
chr16 | 20304574 | 20332513 |
| a0001c0011t0013 | 0/0 | 3337 | 1 | 1 | 0 | 0 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | ATTCC others(3332): Show |
chr16 | 20304574 | 20332513 |
| a0001c0014t0005 | 0/0 | 3337 | 1 | 1 | 0 | 0 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | ATTCC others(3332): Show |
chr16 | 20304574 | 20332513 |
| a0001c0015t0001 | 0/0 | 3339 | 1 | 0 | 1 | 0 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | ATTCC others(3334): Show |
chr16 | 20304574 | 20332513 |
| a0001c0019t0003 | 0/0 | 3337 | 1 | 0 | 1 | 0 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | ATTCC others(3332): Show |
chr16 | 20304574 | 20332513 |
| a0001c0020t0016 | 0/0 | 3338 | 1 | 1 | 0 | 0 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | ATTCC others(3333): Show |
chr16 | 20304574 | 20332513 |
| a0002c0004t0002 | 0/0 | 3338 | 15 | 0 | 0 | 13 | 0 | 2 | GP2_chr16_20304574_20332513 | GP2 | ATTCC others(3333): Show |
chr16 | 20304574 | 20332513 |
| a0002c0004t0003 | 0/0 | 3337 | 1 | 0 | 0 | 1 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | ATTCC others(3332): Show |
chr16 | 20304574 | 20332513 |
| a0002c0004t0015 | 0/0 | 3338 | 1 | 0 | 0 | 1 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | ATTCC others(3333): Show |
chr16 | 20304574 | 20332513 |
| a0002c0004t0020 | 0/0 | 3338 | 1 | 0 | 0 | 0 | 0 | 1 | GP2_chr16_20304574_20332513 | GP2 | ATTCC others(3333): Show |
chr16 | 20304574 | 20332513 |
| a0003c0008t0001 | 0/0 | 3339 | 2 | 0 | 0 | 2 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | ATTCC others(3334): Show |
chr16 | 20304574 | 20332513 |
| a0004c0012t0001 | 0/0 | 3339 | 1 | 0 | 0 | 1 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | ATTCC others(3334): Show |
chr16 | 20304574 | 20332513 |
| a0005c0017t0003 | 0/0 | 3337 | 1 | 0 | 0 | 0 | 1 | 0 | GP2_chr16_20304574_20332513 | GP2 | ATTCC others(3332): Show |
chr16 | 20304574 | 20332513 |
| a0006c0016t0001 | 0/0 | 3339 | 1 | 0 | 0 | 1 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | ATTCC others(3334): Show |
chr16 | 20304574 | 20332513 |
| a0007c0018t0023 | 0/0 | 3338 | 1 | 0 | 0 | 1 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | ATTCC others(3333): Show |
chr16 | 20304574 | 20332513 |
| a0008c0013t0002 | 0/0 | 3338 | 1 | 0 | 1 | 0 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | ATTCC others(3333): Show |
chr16 | 20304574 | 20332513 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 44 | 0 | 5 | 36 | 0 | 3 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0001t0001g0007 | 0/0 | 9 | 0 | 0 | 5 | 0 | 4 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0001t0001g0009 | 0/0 | 8 | 0 | 0 | 7 | 0 | 1 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0001t0001g0011 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0001t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0001t0003g0002 | 0/1 | 17 | 0 | 8 | 0 | 4 | 4 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0001t0003g0006 | 0/0 | 12 | 6 | 3 | 1 | 0 | 2 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0001t0003g0012 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0001t0003g0018 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0001t0003g0025 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0001t0003g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0001t0003g0042 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0001t0003g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0001t0003g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0001t0003g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0001t0003g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0001t0003g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0001t0003g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0001t0003g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0001t0003g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0001t0003g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0001t0003g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0001t0003g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0001t0003g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0001t0003g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0001t0003g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0001t0003g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0001t0003g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0001t0003g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0001t0003g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0001t0003g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0001t0003g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0001t0003g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0001t0003g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0001t0003g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0001t0003g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0001t0004g0004 | 0/0 | 14 | 1 | 2 | 11 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0001t0004g0008 | 1/0 | 8 | 0 | 7 | 0 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0001t0004g0014 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0001t0004g0022 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0001t0004g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0001t0004g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0001t0004g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0001t0004g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0001t0004g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0001t0004g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0001t0004g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0001t0004g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0001t0004g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0001t0004g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0001t0004g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0001t0004g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0001t0004g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0001t0004g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0001t0004g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0001t0004g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0001t0005g0046 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0001t0006g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0001t0007g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0001t0008g0017 | 0/0 | 4 | 1 | 2 | 0 | 0 | 1 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0001t0008g0026 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0001t0008g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0001t0009g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0001t0009g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0001t0009g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0001t0009g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0001t0009g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0001t0009g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0001t0010g0015 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0001t0011g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0001t0011g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0001t0011g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0001t0013g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0001t0014g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0001t0014g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0001t0017g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0001t0019g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0001t0021g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0001t0022g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0001t0024g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0002t0002g0003 | 0/0 | 16 | 0 | 4 | 3 | 2 | 7 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0002t0002g0010 | 0/0 | 7 | 0 | 2 | 1 | 1 | 3 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0002t0002g0016 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0002t0002g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0002t0002g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0002t0002g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0002t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0002t0002g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0002t0002g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0002t0002g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0002t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0002t0002g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0002t0002g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0002t0002g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0002t0002g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0002t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0002t0003g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0002t0003g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0002t0005g0023 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0002t0005g0024 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0002t0005g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0002t0005g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0002t0018g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0003t0002g0020 | 0/0 | 4 | 0 | 2 | 0 | 1 | 1 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0003t0002g0021 | 0/0 | 4 | 1 | 3 | 0 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0003t0002g0027 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0003t0002g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0003t0002g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0003t0002g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0003t0002g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0003t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0003t0002g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0003t0002g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0003t0002g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0003t0002g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0005t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0005t0002g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0005t0006g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0005t0006g0049 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0005t0006g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0005t0006g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0005t0007g0013 | 0/0 | 6 | 4 | 2 | 0 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0005t0007g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0005t0007g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0006t0006g0028 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0006t0012g0029 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0007t0002g0019 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0007t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0007t0003g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0009t0005g0047 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0010t0003g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0011t0013g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0014t0005g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0015t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0019t0003g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0001c0020t0016g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0002c0004t0002g0005 | 0/0 | 14 | 0 | 0 | 12 | 0 | 2 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0002c0004t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0002c0004t0003g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0002c0004t0015g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0002c0004t0020g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0003c0008t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0004c0012t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0005c0017t0003g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0006c0016t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0007c0018t0023g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| a0008c0013t0002g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0003 | g0002 | EUR | GBR | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG00099 | hp2 | a0001 | c0002 | t0002 | g0108 | EUR | GBR | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG00140 | hp1 | a0001 | c0002 | t0002 | g0115 | EUR | GBR | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG00140 | hp2 | a0005 | c0017 | t0003 | g0142 | EUR | GBR | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG00280 | hp1 | a0001 | c0003 | t0002 | g0122 | EUR | FIN | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG00280 | hp2 | a0001 | c0003 | t0002 | g0020 | EUR | FIN | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG00323 | hp1 | a0001 | c0003 | t0002 | g0124 | EUR | FIN | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG00323 | hp2 | a0001 | c0003 | t0002 | g0123 | EUR | FIN | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG00408 | hp1 | a0001 | c0001 | t0014 | g0128 | EAS | CHS | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | CHS | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | CHS | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG00438 | hp1 | a0001 | c0002 | t0002 | g0129 | EAS | CHS | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG00438 | hp2 | a0001 | c0001 | t0010 | g0015 | EAS | CHS | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG00558 | hp1 | a0002 | c0004 | t0002 | g0005 | EAS | CHS | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG00558 | hp2 | a0001 | c0001 | t0004 | g0037 | EAS | CHS | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG00597 | hp2 | a0001 | c0002 | t0002 | g0041 | EAS | CHS | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | CHS | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG00621 | hp2 | a0002 | c0004 | t0002 | g0005 | EAS | CHS | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG00639 | hp1 | a0001 | c0003 | t0002 | g0020 | AMR | PUR | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG00639 | hp2 | a0001 | c0001 | t0003 | g0002 | AMR | PUR | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG00642 | hp1 | a0001 | c0001 | t0003 | g0139 | AMR | PUR | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG00642 | hp2 | a0008 | c0013 | t0002 | g0154 | AMR | PUR | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG00673 | hp2 | a0001 | c0001 | t0004 | g0004 | EAS | CHS | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG00738 | hp1 | a0001 | c0003 | t0002 | g0127 | AMR | PUR | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG00738 | hp2 | a0001 | c0001 | t0003 | g0002 | AMR | PUR | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG00741 | hp1 | a0001 | c0002 | t0002 | g0083 | AMR | PUR | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG00741 | hp2 | a0001 | c0001 | t0004 | g0054 | AMR | PUR | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG01069 | hp1 | a0001 | c0001 | t0004 | g0004 | AMR | PUR | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0101 | AMR | PUR | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG01071 | hp1 | a0001 | c0003 | t0002 | g0021 | AMR | PUR | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG01071 | hp2 | a0001 | c0001 | t0004 | g0004 | AMR | PUR | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG01074 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | PUR | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG01074 | hp2 | a0001 | c0001 | t0003 | g0002 | AMR | PUR | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG01081 | hp1 | a0001 | c0001 | t0003 | g0006 | AMR | PUR | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG01081 | hp2 | a0001 | c0001 | t0003 | g0145 | AMR | PUR | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG01099 | hp1 | a0001 | c0006 | t0012 | g0029 | AMR | PUR | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG01099 | hp2 | a0001 | c0001 | t0008 | g0017 | AMR | PUR | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG01106 | hp1 | a0001 | c0002 | t0002 | g0003 | AMR | PUR | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG01106 | hp2 | a0001 | c0001 | t0003 | g0002 | AMR | PUR | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG01109 | hp1 | a0001 | c0009 | t0005 | g0047 | AMR | PUR | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG01109 | hp2 | a0001 | c0001 | t0003 | g0134 | AMR | PUR | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG01167 | hp1 | a0001 | c0003 | t0002 | g0021 | AMR | PUR | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG01167 | hp2 | a0001 | c0002 | t0002 | g0010 | AMR | PUR | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG01168 | hp1 | a0001 | c0001 | t0003 | g0042 | AMR | PUR | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG01168 | hp2 | a0001 | c0002 | t0002 | g0003 | AMR | PUR | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG01169 | hp1 | a0001 | c0003 | t0002 | g0160 | AMR | PUR | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG01169 | hp2 | a0001 | c0001 | t0003 | g0002 | AMR | PUR | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG01175 | hp1 | a0001 | c0005 | t0007 | g0013 | AMR | PUR | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG01175 | hp2 | a0001 | c0001 | t0003 | g0006 | AMR | PUR | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG01192 | hp1 | a0001 | c0003 | t0002 | g0027 | AMR | PUR | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG01192 | hp2 | a0001 | c0001 | t0004 | g0022 | AMR | PUR | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG01243 | hp1 | a0001 | c0002 | t0002 | g0116 | AMR | PUR | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG01255 | hp1 | a0001 | c0001 | t0003 | g0135 | AMR | CLM | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | CLM | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG01256 | hp1 | a0001 | c0015 | t0001 | g0089 | AMR | CLM | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG01256 | hp2 | a0001 | c0001 | t0003 | g0042 | AMR | CLM | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG01257 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | CLM | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | CLM | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG01261 | hp1 | a0001 | c0002 | t0005 | g0024 | AMR | CLM | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG01346 | hp1 | a0001 | c0003 | t0002 | g0020 | AMR | CLM | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG01346 | hp2 | a0001 | c0001 | t0004 | g0008 | AMR | CLM | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG01358 | hp1 | a0001 | c0001 | t0003 | g0006 | AMR | CLM | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG01358 | hp2 | a0001 | c0002 | t0002 | g0003 | AMR | CLM | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG01361 | hp1 | a0001 | c0001 | t0003 | g0138 | AMR | CLM | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG01361 | hp2 | a0001 | c0001 | t0003 | g0025 | AMR | CLM | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG01433 | hp1 | a0001 | c0005 | t0007 | g0013 | AMR | CLM | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG01496 | hp1 | a0001 | c0001 | t0003 | g0070 | AMR | CLM | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG01496 | hp2 | a0001 | c0001 | t0004 | g0008 | AMR | CLM | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG01515 | hp1 | a0001 | c0002 | t0002 | g0010 | EUR | IBS | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG01515 | hp2 | a0001 | c0001 | t0003 | g0002 | EUR | IBS | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG01516 | hp1 | a0001 | c0002 | t0002 | g0003 | EUR | IBS | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG01516 | hp2 | a0001 | c0002 | t0005 | g0023 | EUR | IBS | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG01517 | hp1 | a0001 | c0002 | t0002 | g0003 | EUR | IBS | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG01517 | hp2 | a0001 | c0001 | t0003 | g0002 | EUR | IBS | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG01884 | hp1 | a0001 | c0001 | t0003 | g0038 | AFR | ACB | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG01884 | hp2 | a0001 | c0005 | t0007 | g0170 | AFR | ACB | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG01891 | hp1 | a0001 | c0014 | t0005 | g0131 | AFR | ACB | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG01891 | hp2 | a0001 | c0001 | t0003 | g0045 | AFR | ACB | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG01928 | hp1 | a0001 | c0001 | t0004 | g0008 | AMR | PEL | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG01928 | hp2 | a0001 | c0003 | t0002 | g0173 | AMR | PEL | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG01934 | hp1 | a0001 | c0001 | t0010 | g0015 | AMR | PEL | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG01934 | hp2 | a0001 | c0019 | t0003 | g0171 | AMR | PEL | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG01943 | hp1 | a0001 | c0001 | t0004 | g0008 | AMR | PEL | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG01943 | hp2 | a0001 | c0001 | t0010 | g0015 | AMR | PEL | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG01975 | hp2 | a0001 | c0001 | t0004 | g0056 | AMR | PEL | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG01978 | hp1 | a0001 | c0001 | t0004 | g0008 | AMR | PEL | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG01978 | hp2 | a0001 | c0003 | t0002 | g0027 | AMR | PEL | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG01981 | hp1 | a0001 | c0003 | t0002 | g0027 | AMR | PEL | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG01981 | hp2 | a0001 | c0002 | t0002 | g0010 | AMR | PEL | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG01993 | hp1 | a0001 | c0001 | t0008 | g0017 | AMR | PEL | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG01993 | hp2 | a0001 | c0002 | t0005 | g0023 | AMR | PEL | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG02004 | hp1 | a0001 | c0001 | t0024 | g0055 | AMR | PEL | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | PEL | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | KHV | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG02015 | hp2 | a0003 | c0008 | t0001 | g0034 | EAS | KHV | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG02027 | hp1 | a0001 | c0002 | t0002 | g0016 | EAS | KHV | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG02027 | hp2 | a0001 | c0001 | t0021 | g0120 | EAS | KHV | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG02040 | hp1 | a0001 | c0002 | t0002 | g0104 | EAS | KHV | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG02071 | hp2 | a0003 | c0008 | t0001 | g0034 | EAS | KHV | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | KHV | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | KHV | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG02129 | hp1 | a0001 | c0002 | t0002 | g0010 | EAS | KHV | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG02132 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | KHV | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG02145 | hp1 | a0001 | c0001 | t0008 | g0026 | AFR | ACB | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG02145 | hp2 | a0001 | c0002 | t0005 | g0151 | AFR | ACB | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | PEL | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG02148 | hp2 | a0001 | c0001 | t0004 | g0053 | AMR | PEL | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG02155 | hp1 | a0001 | c0002 | t0002 | g0036 | EAS | CDX | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG02155 | hp2 | a0001 | c0001 | t0003 | g0025 | EAS | CDX | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG02165 | hp2 | a0001 | c0002 | t0002 | g0040 | EAS | CDX | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG02257 | hp1 | a0001 | c0001 | t0003 | g0045 | AFR | ACB | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG02257 | hp2 | a0001 | c0005 | t0002 | g0068 | AFR | ACB | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG02258 | hp1 | a0001 | c0001 | t0009 | g0048 | AFR | ACB | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0069 | AFR | ACB | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG02273 | hp2 | a0001 | c0001 | t0004 | g0008 | AMR | PEL | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG02280 | hp1 | a0001 | c0001 | t0003 | g0018 | AFR | ACB | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG02280 | hp2 | a0001 | c0001 | t0003 | g0067 | AFR | ACB | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG02293 | hp1 | a0001 | c0001 | t0004 | g0008 | AMR | PEL | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG02293 | hp2 | a0001 | c0001 | t0003 | g0087 | AMR | PEL | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG02300 | hp1 | a0001 | c0003 | t0002 | g0021 | AMR | PEL | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG02300 | hp2 | a0001 | c0001 | t0003 | g0146 | AMR | PEL | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG02451 | hp1 | a0001 | c0001 | t0003 | g0012 | AFR | ACB | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG02451 | hp2 | a0001 | c0001 | t0009 | g0152 | AFR | ACB | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG02523 | hp1 | a0006 | c0016 | t0001 | g0092 | EAS | KHV | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG02602 | hp2 | a0002 | c0004 | t0002 | g0005 | SAS | PJL | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG02615 | hp1 | a0001 | c0005 | t0002 | g0169 | AFR | GWD | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG02615 | hp2 | a0001 | c0001 | t0003 | g0012 | AFR | GWD | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG02622 | hp1 | a0001 | c0007 | t0002 | g0019 | AFR | GWD | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG02622 | hp2 | a0001 | c0001 | t0013 | g0114 | AFR | GWD | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG02630 | hp1 | a0001 | c0005 | t0007 | g0013 | AFR | GWD | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG02630 | hp2 | a0001 | c0001 | t0003 | g0143 | AFR | GWD | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG02647 | hp1 | a0001 | c0001 | t0003 | g0018 | AFR | GWD | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG02647 | hp2 | a0001 | c0007 | t0002 | g0019 | AFR | GWD | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG02683 | hp1 | a0001 | c0003 | t0002 | g0020 | SAS | PJL | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG02683 | hp2 | a0001 | c0001 | t0003 | g0002 | SAS | PJL | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG02698 | hp1 | a0001 | c0001 | t0003 | g0006 | SAS | PJL | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG02698 | hp2 | a0001 | c0001 | t0005 | g0046 | SAS | PJL | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG02717 | hp1 | a0001 | c0001 | t0017 | g0085 | AFR | GWD | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG02717 | hp2 | a0001 | c0005 | t0007 | g0013 | AFR | GWD | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG02723 | hp1 | a0001 | c0001 | t0022 | g0132 | AFR | GWD | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG02723 | hp2 | a0001 | c0001 | t0003 | g0006 | AFR | GWD | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG02735 | hp2 | a0001 | c0002 | t0002 | g0003 | SAS | PJL | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG02738 | hp1 | a0001 | c0010 | t0003 | g0075 | SAS | PJL | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG02738 | hp2 | a0001 | c0001 | t0003 | g0002 | SAS | PJL | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG02809 | hp1 | a0001 | c0005 | t0006 | g0044 | AFR | GWD | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG02809 | hp2 | a0001 | c0007 | t0002 | g0072 | AFR | GWD | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG02818 | hp1 | a0001 | c0005 | t0007 | g0164 | AFR | GWD | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG02818 | hp2 | a0001 | c0001 | t0003 | g0006 | AFR | GWD | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG02886 | hp1 | a0001 | c0001 | t0009 | g0150 | AFR | GWD | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG02886 | hp2 | a0001 | c0001 | t0009 | g0153 | AFR | GWD | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG02895 | hp1 | a0001 | c0007 | t0003 | g0074 | AFR | GWD | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG02895 | hp2 | a0001 | c0005 | t0006 | g0049 | AFR | GWD | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG02896 | hp1 | a0001 | c0001 | t0003 | g0043 | AFR | GWD | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG02896 | hp2 | a0001 | c0001 | t0003 | g0140 | AFR | GWD | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG02897 | hp1 | a0001 | c0001 | t0003 | g0043 | AFR | GWD | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG02897 | hp2 | a0001 | c0005 | t0006 | g0049 | AFR | GWD | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG02922 | hp1 | a0001 | c0001 | t0003 | g0038 | AFR | ESN | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG02922 | hp2 | a0001 | c0009 | t0005 | g0047 | AFR | ESN | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG02965 | hp1 | a0001 | c0005 | t0007 | g0013 | AFR | ESN | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG02965 | hp2 | a0001 | c0002 | t0005 | g0088 | AFR | ESN | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG02970 | hp1 | a0001 | c0007 | t0002 | g0019 | AFR | ESN | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG02970 | hp2 | a0001 | c0002 | t0005 | g0024 | AFR | ESN | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG02976 | hp1 | a0001 | c0001 | t0003 | g0162 | AFR | ESN | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG02976 | hp2 | a0001 | c0006 | t0006 | g0028 | AFR | ESN | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG03041 | hp1 | a0001 | c0001 | t0006 | g0155 | AFR | GWD | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG03041 | hp2 | a0001 | c0001 | t0003 | g0141 | AFR | GWD | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG03098 | hp1 | a0001 | c0001 | t0003 | g0018 | AFR | MSL | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG03098 | hp2 | a0001 | c0005 | t0006 | g0166 | AFR | MSL | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG03139 | hp1 | a0001 | c0002 | t0018 | g0172 | AFR | ESN | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG03139 | hp2 | a0001 | c0001 | t0003 | g0051 | AFR | ESN | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG03195 | hp1 | a0001 | c0001 | t0003 | g0012 | AFR | ESN | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG03195 | hp2 | a0001 | c0006 | t0012 | g0029 | AFR | ESN | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG03209 | hp1 | a0001 | c0001 | t0003 | g0012 | AFR | MSL | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG03209 | hp2 | a0001 | c0011 | t0013 | g0161 | AFR | MSL | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG03225 | hp1 | a0001 | c0005 | t0007 | g0013 | AFR | MSL | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG03225 | hp2 | a0001 | c0001 | t0003 | g0012 | AFR | MSL | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG03239 | hp1 | a0001 | c0003 | t0002 | g0126 | SAS | PJL | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG03239 | hp2 | a0001 | c0002 | t0002 | g0003 | SAS | PJL | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG03453 | hp1 | a0001 | c0006 | t0006 | g0028 | AFR | MSL | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG03453 | hp2 | a0001 | c0001 | t0003 | g0006 | AFR | MSL | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG03486 | hp1 | a0001 | c0006 | t0012 | g0029 | AFR | MSL | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG03486 | hp2 | a0001 | c0001 | t0003 | g0006 | AFR | MSL | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG03490 | hp2 | a0001 | c0001 | t0003 | g0006 | SAS | PJL | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG03491 | hp1 | a0001 | c0001 | t0011 | g0118 | SAS | PJL | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG03491 | hp2 | a0001 | c0001 | t0008 | g0017 | SAS | PJL | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0119 | SAS | PJL | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG03516 | hp1 | a0001 | c0001 | t0003 | g0012 | AFR | ESN | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG03516 | hp2 | a0001 | c0002 | t0005 | g0024 | AFR | ESN | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG03540 | hp1 | a0001 | c0001 | t0003 | g0018 | AFR | GWD | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG03540 | hp2 | a0001 | c0006 | t0006 | g0028 | AFR | GWD | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG03579 | hp1 | a0001 | c0001 | t0008 | g0017 | AFR | MSL | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG03579 | hp2 | a0001 | c0001 | t0003 | g0133 | AFR | MSL | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG03654 | hp1 | a0001 | c0001 | t0019 | g0073 | SAS | PJL | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0082 | SAS | PJL | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG03669 | hp1 | a0001 | c0002 | t0002 | g0106 | SAS | PJL | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG03669 | hp2 | a0001 | c0002 | t0002 | g0003 | SAS | PJL | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG03688 | hp1 | a0001 | c0001 | t0003 | g0060 | SAS | STU | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0078 | SAS | STU | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG03704 | hp1 | a0001 | c0001 | t0003 | g0002 | SAS | PJL | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG03704 | hp2 | a0002 | c0004 | t0020 | g0103 | SAS | PJL | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG03710 | hp1 | a0001 | c0002 | t0002 | g0010 | SAS | PJL | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG03710 | hp2 | a0001 | c0001 | t0004 | g0057 | SAS | PJL | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0081 | SAS | BEB | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG03831 | hp2 | a0001 | c0001 | t0004 | g0066 | SAS | BEB | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | BEB | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG03834 | hp2 | a0001 | c0002 | t0002 | g0003 | SAS | BEB | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG03927 | hp1 | a0001 | c0002 | t0002 | g0010 | SAS | BEB | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG03927 | hp2 | a0001 | c0001 | t0005 | g0046 | SAS | BEB | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG03942 | hp2 | a0001 | c0002 | t0002 | g0003 | SAS | BEB | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG04115 | hp1 | a0002 | c0004 | t0002 | g0005 | SAS | STU | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG04115 | hp2 | a0001 | c0002 | t0002 | g0076 | SAS | STU | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG04199 | hp1 | a0001 | c0002 | t0002 | g0003 | SAS | STU | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG04199 | hp2 | a0001 | c0001 | t0003 | g0002 | SAS | STU | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | STU | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | STU | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG04228 | hp1 | a0001 | c0002 | t0002 | g0003 | SAS | STU | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0086 | SAS | STU | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| NA18612 | hp1 | a0001 | c0001 | t0010 | g0015 | EAS | CHB | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | CHB | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| NA18939 | hp2 | a0002 | c0004 | t0002 | g0167 | EAS | JPT | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| NA18941 | hp2 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| NA18945 | hp2 | a0001 | c0001 | t0004 | g0065 | EAS | JPT | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| NA18946 | hp1 | a0002 | c0004 | t0003 | g0165 | EAS | JPT | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| NA18946 | hp2 | a0001 | c0002 | t0003 | g0109 | EAS | JPT | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| NA18947 | hp1 | a0002 | c0004 | t0002 | g0005 | EAS | JPT | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| NA18947 | hp2 | a0001 | c0001 | t0004 | g0063 | EAS | JPT | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| NA18950 | hp1 | a0001 | c0001 | t0004 | g0062 | EAS | JPT | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| NA18950 | hp2 | a0001 | c0001 | t0011 | g0091 | EAS | JPT | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| NA18956 | hp1 | a0007 | c0018 | t0023 | g0105 | EAS | JPT | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| NA18956 | hp2 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| NA18959 | hp1 | a0001 | c0001 | t0004 | g0014 | EAS | JPT | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| NA18959 | hp2 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| NA18961 | hp1 | a0001 | c0001 | t0003 | g0136 | EAS | JPT | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| NA18961 | hp2 | a0001 | c0002 | t0002 | g0016 | EAS | JPT | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| NA18962 | hp2 | a0001 | c0002 | t0002 | g0016 | EAS | JPT | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| NA18964 | hp2 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| NA18966 | hp1 | a0002 | c0004 | t0002 | g0005 | EAS | JPT | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| NA18968 | hp1 | a0001 | c0001 | t0004 | g0061 | EAS | JPT | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| NA18970 | hp2 | a0001 | c0001 | t0004 | g0050 | EAS | JPT | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| NA18971 | hp1 | a0002 | c0004 | t0015 | g0168 | EAS | JPT | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| NA18971 | hp2 | a0001 | c0002 | t0002 | g0036 | EAS | JPT | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| NA18972 | hp2 | a0002 | c0004 | t0002 | g0005 | EAS | JPT | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| NA18974 | hp2 | a0001 | c0001 | t0004 | g0037 | EAS | JPT | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| NA18975 | hp1 | a0001 | c0001 | t0004 | g0111 | EAS | JPT | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| NA18977 | hp2 | a0001 | c0002 | t0003 | g0117 | EAS | JPT | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| NA18978 | hp1 | a0001 | c0001 | t0004 | g0030 | EAS | JPT | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| NA18979 | hp1 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| NA18983 | hp1 | a0001 | c0001 | t0004 | g0022 | EAS | JPT | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| NA18985 | hp1 | a0001 | c0001 | t0004 | g0058 | EAS | JPT | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| NA18987 | hp1 | a0001 | c0001 | t0003 | g0147 | EAS | JPT | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| NA18989 | hp1 | a0001 | c0002 | t0002 | g0040 | EAS | JPT | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| NA18990 | hp1 | a0002 | c0004 | t0002 | g0005 | EAS | JPT | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| NA18990 | hp2 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| NA18991 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| NA18992 | hp2 | a0001 | c0001 | t0004 | g0022 | EAS | JPT | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| NA18993 | hp1 | a0001 | c0001 | t0003 | g0025 | EAS | JPT | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| NA18993 | hp2 | a0002 | c0004 | t0002 | g0005 | EAS | JPT | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| NA18994 | hp1 | a0001 | c0001 | t0011 | g0079 | EAS | JPT | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| NA18994 | hp2 | a0001 | c0001 | t0004 | g0014 | EAS | JPT | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| NA18999 | hp2 | a0002 | c0004 | t0002 | g0005 | EAS | JPT | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| NA19002 | hp1 | a0004 | c0012 | t0001 | g0077 | EAS | JPT | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| NA19002 | hp2 | a0001 | c0002 | t0002 | g0016 | EAS | JPT | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| NA19003 | hp1 | a0002 | c0004 | t0002 | g0005 | EAS | JPT | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| NA19005 | hp2 | a0001 | c0001 | t0004 | g0030 | EAS | JPT | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| NA19007 | hp1 | a0001 | c0001 | t0004 | g0059 | EAS | JPT | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| NA19010 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| NA19011 | hp2 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| NA19030 | hp1 | a0001 | c0001 | t0003 | g0149 | AFR | LWK | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| NA19030 | hp2 | a0001 | c0003 | t0002 | g0125 | AFR | LWK | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| NA19043 | hp1 | a0001 | c0001 | t0009 | g0144 | AFR | LWK | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| NA19043 | hp2 | a0001 | c0001 | t0008 | g0026 | AFR | LWK | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| NA19054 | hp1 | a0001 | c0001 | t0010 | g0015 | EAS | JPT | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| NA19060 | hp1 | a0002 | c0004 | t0002 | g0005 | EAS | JPT | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| NA19060 | hp2 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| NA19068 | hp1 | a0001 | c0001 | t0004 | g0014 | EAS | JPT | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| NA19068 | hp2 | a0001 | c0002 | t0002 | g0016 | EAS | JPT | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| NA19070 | hp1 | a0001 | c0001 | t0004 | g0052 | EAS | JPT | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| NA19070 | hp2 | a0001 | c0002 | t0002 | g0041 | EAS | JPT | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| NA19079 | hp1 | a0002 | c0004 | t0002 | g0005 | EAS | JPT | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| NA19080 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| NA19081 | hp2 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| NA19084 | hp2 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| NA19085 | hp2 | a0001 | c0002 | t0002 | g0064 | EAS | JPT | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| NA19086 | hp1 | a0001 | c0001 | t0004 | g0014 | EAS | JPT | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| NA19087 | hp1 | a0001 | c0001 | t0014 | g0090 | EAS | JPT | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| NA19087 | hp2 | a0001 | c0001 | t0004 | g0014 | EAS | JPT | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| NA19090 | hp2 | a0002 | c0004 | t0002 | g0005 | EAS | JPT | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| NA19240 | hp1 | a0001 | c0005 | t0006 | g0163 | AFR | YRI | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| NA19240 | hp2 | a0001 | c0007 | t0002 | g0019 | AFR | YRI | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| NA20129 | hp1 | a0001 | c0005 | t0006 | g0044 | AFR | ASW | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| NA20129 | hp2 | a0001 | c0001 | t0004 | g0004 | AFR | ASW | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| NA20752 | hp1 | a0001 | c0001 | t0003 | g0002 | EUR | TSI | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| NA20752 | hp2 | a0001 | c0002 | t0005 | g0023 | EUR | TSI | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| NA20805 | hp1 | a0001 | c0001 | t0003 | g0148 | EUR | TSI | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| NA20805 | hp2 | a0001 | c0003 | t0002 | g0121 | EUR | TSI | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| NA20905 | hp1 | a0001 | c0002 | t0002 | g0010 | SAS | GIH | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| NA20905 | hp2 | a0001 | c0002 | t0002 | g0084 | SAS | GIH | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG01123 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | CLM | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG01123 | hp2 | a0001 | c0002 | t0002 | g0003 | AMR | CLM | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG02109 | hp1 | a0001 | c0001 | t0003 | g0006 | AFR | ACB | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG02109 | hp2 | a0001 | c0001 | t0007 | g0137 | AFR | ACB | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG02486 | hp1 | a0001 | c0001 | t0008 | g0026 | AFR | ACB | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG02486 | hp2 | a0001 | c0001 | t0009 | g0048 | AFR | ACB | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG03471 | hp1 | a0001 | c0001 | t0003 | g0006 | AFR | MSL | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG03471 | hp2 | a0001 | c0001 | t0003 | g0071 | AFR | MSL | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG06807 | hp1 | a0001 | c0001 | t0003 | g0130 | AFR | USA | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| HG06807 | hp2 | a0001 | c0003 | t0002 | g0021 | AFR | USA | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| NA20300 | hp1 | a0001 | c0001 | t0003 | g0012 | AFR | USA | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| NA20300 | hp2 | a0001 | c0020 | t0016 | g0158 | AFR | USA | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| NA21309 | hp1 | a0001 | c0001 | t0008 | g0156 | AFR | LWK | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| NA21309 | hp2 | a0001 | c0001 | t0009 | g0159 | AFR | LWK | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0003 | g0002 | REF | REF | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0004 | g0008 | REF | REF | GP2_chr16_20304574_20332513 | GP2 | chr16 | 20304574 | 20332513 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:20314671 | G | C | 1 | a0003 | 2 | HG02015.hp2 HG02071.hp2 |
missense_variant | MODERATE | c.1532C>G | p.Thr511Ser | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 10/11 | 1615/3337 | 1532/1605 | 511/534 | chr16 | 20314671 | |||
| chr16:20314674 | C | T | 1 | a0005 | 1 | HG00140.hp2 | missense_variant | MODERATE | c.1529G>A | p.Gly510Glu | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 10/11 | 1612/3337 | 1529/1605 | 510/534 | chr16 | 20314674 | |||
| chr16:20314687 | C | T | 1 | a0006 | 1 | HG02523.hp1 | missense_variant | MODERATE | c.1516G>A | p.Gly506Ser | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 10/11 | 1599/3337 | 1516/1605 | 506/534 | chr16 | 20314687 | |||
| chr16:20314698 | G | T | 1 | a0007 | 1 | NA18956.hp1 | missense_variant | MODERATE | c.1505C>A | p.Ala502Glu | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 10/11 | 1588/3337 | 1505/1605 | 502/534 | chr16 | 20314698 | |||
| chr16:20317344 | C | T | 1 | a0002 | 18 | HG00558.hp1 HG00621.hp2 HG02602.hp2 others(15): Show |
missense_variant | MODERATE | c.1285G>A | p.Val429Met | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 8/11 | 1368/3337 | 1285/1605 | 429/534 | chr16 | 20317344 | |||
| chr16:20323942 | C | T | 1 | a0008 | 1 | HG00642.hp2 | missense_variant | MODERATE | c.409G>A | p.Ala137Thr | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 3/11 | 492/3337 | 409/1605 | 137/534 | chr16 | 20323942 | |||
| chr16:20324016 | C | T | 1 | a0004 | 1 | NA19002.hp1 | missense_variant | MODERATE | c.335G>A | p.Arg112Gln | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 3/11 | 418/3337 | 335/1605 | 112/534 | chr16 | 20324016 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:20311280 | C | A | 1 | a0001c0007 | 6 | HG02622.hp1 HG02647.hp2 HG02809.hp2 others(3): Show |
splice_region_variant&synonymous_variant | LOW | c.1548G>T | p.Gly516Gly | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 11/11 | 1631/3337 | 1548/1605 | 516/534 | chr16 | 20311280 | |||
| chr16:20315999 | G | A | 3 | a0001c0009 a0001c0014 a0001c0020 |
4 | HG01109.hp1 HG01891.hp1 HG02922.hp2 others(1): Show |
synonymous_variant | LOW | c.1458C>T | p.Ile486Ile | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 9/11 | 1541/3337 | 1458/1605 | 486/534 | chr16 | 20315999 | |||
| chr16:20317321 | C | G | 1 | a0001c0015 | 1 | HG01256.hp1 | synonymous_variant | LOW | c.1308G>C | p.Ser436Ser | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 8/11 | 1391/3337 | 1308/1605 | 436/534 | chr16 | 20317321 | |||
| chr16:20317363 | T | C | 3 | a0001c0002 a0001c0003 a0007c0018 |
76 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(73): Show |
synonymous_variant | LOW | c.1266A>G | p.Gln422Gln | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 8/11 | 1349/3337 | 1266/1605 | 422/534 | chr16 | 20317363 | |||
| chr16:20320415 | C | G | 5 | a0001c0005 a0001c0006 a0001c0014 others(2): Show |
42 | HG00558.hp1 HG00621.hp2 HG00642.hp2 others(39): Show |
synonymous_variant | LOW | c.705G>C | p.Val235Val | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 5/11 | 788/3337 | 705/1605 | 235/534 | chr16 | 20320415 | |||
| chr16:20324003 | G | A | 1 | a0001c0003 | 20 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(17): Show |
synonymous_variant | LOW | c.348C>T | p.Asp116Asp | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 3/11 | 431/3337 | 348/1605 | 116/534 | chr16 | 20324003 | |||
| chr16:20324039 | C | T | 2 | a0001c0006 a0001c0011 |
7 | HG01099.hp1 HG02976.hp2 HG03195.hp2 others(4): Show |
synonymous_variant | LOW | c.312G>A | p.Ser104Ser | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 3/11 | 395/3337 | 312/1605 | 104/534 | chr16 | 20324039 | |||
| chr16:20324096 | G | A | 2 | a0001c0019 a0001c0020 |
2 | HG01934.hp2 NA20300.hp2 |
synonymous_variant | LOW | c.255C>T | p.Cys85Cys | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 3/11 | 338/3337 | 255/1605 | 85/534 | chr16 | 20324096 | |||
| chr16:20326357 | C | T | 1 | a0001c0010 | 1 | HG02738.hp1 | synonymous_variant | LOW | c.75G>A | p.Gln25Gln | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 2/11 | 158/3337 | 75/1605 | 25/534 | chr16 | 20326357 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:20309655 | C | T | 1 | a0002c0004t0020 | 1 | HG03704.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1568G>A | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 11/11 | 1568 | chr16 | 20309655 | ||||||
| chr16:20309664 | A | G | 30 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(27): Show |
286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
3_prime_UTR_variant | MODIFIER | c.*1559T>C | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 11/11 | 1559 | chr16 | 20309664 | ||||||
| chr16:20309681 | G | T | 1 | a0001c0001t0019 | 1 | HG03654.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1542C>A | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 11/11 | 1542 | chr16 | 20309681 | ||||||
| chr16:20309722 | C | G | 3 | a0001c0001t0007 a0001c0001t0022 a0001c0005t0007 |
10 | HG01175.hp1 HG01433.hp1 HG01884.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1501G>C | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 11/11 | 1501 | chr16 | 20309722 | ||||||
| chr16:20309742 | C | CCAGG | 7 | a0001c0001t0006 a0001c0001t0007 a0001c0001t0022 others(4): Show |
23 | HG01099.hp1 HG01175.hp1 HG01433.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*1477_*1480dupCCTG | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 11/11 | 1480 | chr16 | 20309742 | ||||||
| chr16:20309986 | G | C | 18 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0019 others(15): Show |
173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
3_prime_UTR_variant | MODIFIER | c.*1237C>G | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 11/11 | 1237 | chr16 | 20309986 | ||||||
| chr16:20310092 | T | A | 7 | a0001c0001t0006 a0001c0001t0007 a0001c0001t0022 others(4): Show |
23 | HG01099.hp1 HG01175.hp1 HG01433.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*1131A>T | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 11/11 | 1131 | chr16 | 20310092 | ||||||
| chr16:20310101 | G | A | 43 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(40): Show |
330 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): Show |
3_prime_UTR_variant | MODIFIER | c.*1122C>T | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 11/11 | 1122 | chr16 | 20310101 | ||||||
| chr16:20310145 | C | A | 11 | a0001c0001t0001 a0001c0001t0011 a0001c0001t0013 others(8): Show |
112 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(109): Show |
3_prime_UTR_variant | MODIFIER | c.*1078G>T | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 11/11 | 1078 | chr16 | 20310145 | ||||||
| chr16:20310322 | G | T | 1 | a0001c0001t0010 | 5 | HG00438.hp2 HG01934.hp1 HG01943.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*901C>A | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 11/11 | 901 | chr16 | 20310322 | ||||||
| chr16:20310404 | G | A | 1 | a0001c0006t0012 | 3 | HG01099.hp1 HG03195.hp2 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*819C>T | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 11/11 | 819 | chr16 | 20310404 | ||||||
| chr16:20310602 | T | C | 1 | a0001c0001t0024 | 1 | HG02004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*621A>G | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 11/11 | 621 | chr16 | 20310602 | ||||||
| chr16:20310753 | C | CT | 14 | a0001c0001t0002 a0001c0001t0014 a0001c0001t0019 others(11): Show |
97 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(94): Show |
3_prime_UTR_variant | MODIFIER | c.*469dupA | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 11/11 | 469 | chr16 | 20310753 | ||||||
| chr16:20310753 | C | CTT | 13 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0007 others(10): Show |
127 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(124): Show |
3_prime_UTR_variant | MODIFIER | c.*468_*469dupAA | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 11/11 | 469 | chr16 | 20310753 | ||||||
| chr16:20310825 | C | A | 1 | a0001c0001t0021 | 1 | HG02027.hp2 | 3_prime_UTR_variant | MODIFIER | c.*398G>T | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 11/11 | 398 | chr16 | 20310825 | ||||||
| chr16:20310838 | C | A | 8 | a0001c0001t0001 a0001c0001t0011 a0001c0001t0014 others(5): Show |
109 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(106): Show |
3_prime_UTR_variant | MODIFIER | c.*385G>T | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 11/11 | 385 | chr16 | 20310838 | ||||||
| chr16:20310844 | C | T | 1 | a0001c0020t0016 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*379G>A | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 11/11 | 379 | chr16 | 20310844 | ||||||
| chr16:20310946 | G | A | 7 | a0001c0001t0006 a0001c0001t0007 a0001c0001t0022 others(4): Show |
23 | HG01099.hp1 HG01175.hp1 HG01433.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*277C>T | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 11/11 | 277 | chr16 | 20310946 | ||||||
| chr16:20311048 | C | A | 1 | a0007c0018t0023 | 1 | NA18956.hp1 | 3_prime_UTR_variant | MODIFIER | c.*175G>T | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 11/11 | 175 | chr16 | 20311048 | ||||||
| chr16:20311103 | T | C | 44 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(41): Show |
338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
3_prime_UTR_variant | MODIFIER | c.*120A>G | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 11/11 | 120 | chr16 | 20311103 | ||||||
| chr16:20311106 | G | T | 1 | a0002c0004t0015 | 1 | NA18971.hp1 | 3_prime_UTR_variant | MODIFIER | c.*117C>A | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 11/11 | 117 | chr16 | 20311106 | ||||||
| chr16:20311117 | A | G | 42 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(39): Show |
323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
3_prime_UTR_variant | MODIFIER | c.*106T>C | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 11/11 | 106 | chr16 | 20311117 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:20311376 | G | C | 1 | a0001c0001t0011g0079 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1547-95C>G | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 10/10 | chr16 | 20311376 | |||||||
| chr16:20311787 | C | T | 1 | a0001c0001t0004g0058 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1547-506G>A | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 10/10 | chr16 | 20311787 | |||||||
| chr16:20311788 | G | A | 1 | a0001c0001t0005g0046 | 2 | HG02698.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.1547-507C>T | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 10/10 | chr16 | 20311788 | |||||||
| chr16:20311820 | T | C | 1 | a0001c0002t0002g0083 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1547-539A>G | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 10/10 | chr16 | 20311820 | |||||||
| chr16:20311846 | G | A | 6 | a0002c0004t0002g0005 a0002c0004t0002g0167 a0002c0004t0003g0165 others(3): Show |
19 | HG00558.hp1 HG00621.hp2 HG00642.hp2 others(16): Show |
intron_variant | MODIFIER | c.1547-565C>T | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 10/10 | chr16 | 20311846 | |||||||
| chr16:20312113 | G | T | 1 | a0001c0001t0001g0096 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1547-832C>A | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 10/10 | chr16 | 20312113 | |||||||
| chr16:20312329 | G | A | 11 | a0001c0001t0006g0155 a0001c0001t0007g0137 a0001c0005t0006g0044 others(8): Show |
22 | HG01099.hp1 HG01175.hp1 HG01433.hp1 others(19): Show |
intron_variant | MODIFIER | c.1547-1048C>T | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 10/10 | chr16 | 20312329 | |||||||
| chr16:20312510 | G | A | 1 | a0001c0001t0001g0098 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1547-1229C>T | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 10/10 | chr16 | 20312510 | |||||||
| chr16:20312520 | G | A | 2 | a0001c0001t0009g0150 a0001c0002t0018g0172 |
2 | HG02886.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1547-1239C>T | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 10/10 | chr16 | 20312520 | |||||||
| chr16:20312617 | C | T | 1 | a0001c0001t0017g0085 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1547-1336G>A | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 10/10 | chr16 | 20312617 | |||||||
| chr16:20312637 | G | A | 1 | a0001c0003t0002g0126 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1547-1356C>T | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 10/10 | chr16 | 20312637 | |||||||
| chr16:20312656 | C | CT | 19 | a0001c0001t0002g0069 a0001c0001t0003g0018 a0001c0001t0003g0070 others(16): Show |
34 | HG01099.hp1 HG01175.hp1 HG01433.hp1 others(31): Show |
intron_variant | MODIFIER | c.1547-1376dupA | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 10/10 | chr16 | 20312656 | |||||||
| chr16:20312728 | G | A | 1 | a0001c0001t0001g0035 | 2 | NA18979.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.1547-1447C>T | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 10/10 | chr16 | 20312728 | |||||||
| chr16:20312856 | G | T | 1 | a0001c0001t0001g0095 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1547-1575C>A | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 10/10 | chr16 | 20312856 | |||||||
| chr16:20312956 | G | A | 1 | a0001c0003t0002g0127 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1547-1675C>T | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 10/10 | chr16 | 20312956 | |||||||
| chr16:20313016 | G | A | 11 | a0001c0001t0006g0155 a0001c0001t0007g0137 a0001c0005t0006g0044 others(8): Show |
22 | HG01099.hp1 HG01175.hp1 HG01433.hp1 others(19): Show |
intron_variant | MODIFIER | c.1546+1641C>T | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 10/10 | chr16 | 20313016 | |||||||
| chr16:20313079 | T | C | 14 | a0001c0001t0003g0002 a0001c0001t0003g0025 a0001c0001t0003g0042 others(11): Show |
33 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(30): Show |
intron_variant | MODIFIER | c.1546+1578A>G | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 10/10 | chr16 | 20313079 | |||||||
| chr16:20313243 | C | G | 3 | a0001c0001t0003g0012 a0001c0001t0003g0133 a0001c0001t0022g0132 |
9 | HG02451.hp1 HG02615.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.1546+1414G>C | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 10/10 | chr16 | 20313243 | |||||||
| chr16:20313249 | C | G | 2 | a0001c0001t0003g0038 a0001c0019t0003g0171 |
3 | HG01884.hp1 HG01934.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1546+1408G>C | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 10/10 | chr16 | 20313249 | |||||||
| chr16:20313251 | CTG | C | 2 | a0001c0001t0003g0038 a0001c0019t0003g0171 |
3 | HG01884.hp1 HG01934.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1546+1404_1546+140 others(6): Show |
GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 10/10 | chr16 | 20313251 | |||||||
| chr16:20313259 | C | G | 2 | a0001c0001t0003g0038 a0001c0019t0003g0171 |
3 | HG01884.hp1 HG01934.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1546+1398G>C | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 10/10 | chr16 | 20313259 | |||||||
| chr16:20313261 | G | C | 2 | a0001c0001t0003g0038 a0001c0019t0003g0171 |
3 | HG01884.hp1 HG01934.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1546+1396C>G | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 10/10 | chr16 | 20313261 | |||||||
| chr16:20313261 | G | GTC | 78 | a0001c0001t0002g0069 a0001c0001t0002g0086 a0001c0001t0003g0002 others(75): Show |
171 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(168): Show |
intron_variant | MODIFIER | c.1546+1394_1546+139 others(6): Show |
GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 10/10 | chr16 | 20313261 | |||||||
| chr16:20313436 | A | G | 1 | a0001c0001t0001g0094 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1546+1221T>C | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 10/10 | chr16 | 20313436 | |||||||
| chr16:20313541 | C | T | 5 | a0001c0002t0005g0023 a0001c0002t0005g0024 a0001c0002t0005g0088 others(2): Show |
9 | HG01261.hp1 HG01516.hp2 HG01993.hp2 others(6): Show |
intron_variant | MODIFIER | c.1546+1116G>A | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 10/10 | chr16 | 20313541 | |||||||
| chr16:20313542 | G | A | 1 | a0001c0001t0005g0046 | 2 | HG02698.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.1546+1115C>T | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 10/10 | chr16 | 20313542 | |||||||
| chr16:20313671 | C | A | 4 | a0001c0001t0005g0046 a0001c0009t0005g0047 a0001c0014t0005g0131 others(1): Show |
6 | HG01109.hp1 HG01891.hp1 HG02698.hp2 others(3): Show |
intron_variant | MODIFIER | c.1546+986G>T | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 10/10 | chr16 | 20313671 | |||||||
| chr16:20314058 | C | T | 1 | a0001c0001t0001g0078 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1546+599G>A | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 10/10 | chr16 | 20314058 | |||||||
| chr16:20314129 | A | G | 1 | a0001c0002t0002g0115 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1546+528T>C | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 10/10 | chr16 | 20314129 | |||||||
| chr16:20314239 | A | G | 2 | a0001c0001t0003g0038 a0001c0019t0003g0171 |
3 | HG01884.hp1 HG01934.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1546+418T>C | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 10/10 | chr16 | 20314239 | |||||||
| chr16:20314245 | T | TA | 40 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(37): Show |
111 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.1546+411dupT | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 10/10 | chr16 | 20314245 | |||||||
| chr16:20314267 | A | C | 3 | a0001c0001t0003g0012 a0001c0001t0003g0133 a0001c0001t0022g0132 |
9 | HG02451.hp1 HG02615.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.1546+390T>G | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 10/10 | chr16 | 20314267 | |||||||
| chr16:20314293 | C | CT | 41 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(38): Show |
112 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.1546+363dupA | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 10/10 | chr16 | 20314293 | |||||||
| chr16:20314360 | T | A | 2 | a0001c0001t0009g0048 a0001c0001t0009g0144 |
3 | HG02258.hp1 HG02486.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1546+297A>T | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 10/10 | chr16 | 20314360 | |||||||
| chr16:20314514 | T | C | 1 | a0001c0001t0005g0046 | 2 | HG02698.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.1546+143A>G | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 10/10 | chr16 | 20314514 | |||||||
| chr16:20314614 | A | G | 1 | a0001c0002t0002g0106 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1546+43T>C | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 10/10 | chr16 | 20314614 | |||||||
| chr16:20314851 | C | T | 1 | a0001c0002t0002g0036 | 2 | HG02155.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.1502-150G>A | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 9/10 | chr16 | 20314851 | |||||||
| chr16:20314863 | T | C | 1 | a0008c0013t0002g0154 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1502-162A>G | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 9/10 | chr16 | 20314863 | |||||||
| chr16:20314874 | T | C | 4 | a0001c0003t0002g0122 a0001c0003t0002g0123 a0001c0003t0002g0125 others(1): Show |
4 | HG00280.hp1 HG00323.hp2 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.1502-173A>G | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 9/10 | chr16 | 20314874 | |||||||
| chr16:20315071 | C | T | 1 | a0001c0020t0016g0158 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1502-370G>A | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 9/10 | chr16 | 20315071 | |||||||
| chr16:20315085 | C | T | 54 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(51): Show |
136 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.1502-384G>A | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 9/10 | chr16 | 20315085 | |||||||
| chr16:20315275 | T | C | 1 | a0001c0005t0006g0163 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1502-574A>G | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 9/10 | chr16 | 20315275 | |||||||
| chr16:20315276 | T | C | 2 | a0001c0001t0003g0145 a0001c0010t0003g0075 |
2 | HG01081.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.1502-575A>G | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 9/10 | chr16 | 20315276 | |||||||
| chr16:20315279 | T | C | 1 | a0001c0001t0005g0046 | 2 | HG02698.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.1502-578A>G | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 9/10 | chr16 | 20315279 | |||||||
| chr16:20315405 | A | G | 2 | a0001c0001t0001g0119 a0001c0001t0011g0118 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1501+551T>C | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 9/10 | chr16 | 20315405 | |||||||
| chr16:20315464 | A | T | 1 | a0001c0001t0011g0091 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1501+492T>A | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 9/10 | chr16 | 20315464 | |||||||
| chr16:20315529 | C | T | 4 | a0001c0002t0005g0023 a0001c0002t0005g0024 a0001c0002t0005g0088 others(1): Show |
8 | HG01261.hp1 HG01516.hp2 HG01993.hp2 others(5): Show |
intron_variant | MODIFIER | c.1501+427G>A | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 9/10 | chr16 | 20315529 | |||||||
| chr16:20315589 | C | G | 1 | a0001c0002t0005g0023 | 3 | HG01516.hp2 HG01993.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1501+367G>C | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 9/10 | chr16 | 20315589 | |||||||
| chr16:20315755 | G | A | 3 | a0001c0001t0001g0009 a0001c0001t0001g0098 a0001c0001t0001g0102 |
10 | HG00597.hp1 HG02735.hp1 NA18951.hp1 others(7): Show |
intron_variant | MODIFIER | c.1501+201C>T | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 9/10 | chr16 | 20315755 | |||||||
| chr16:20315759 | G | T | 1 | a0001c0001t0003g0141 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1501+197C>A | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 9/10 | chr16 | 20315759 | |||||||
| chr16:20315853 | G | A | 1 | a0001c0001t0003g0146 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1501+103C>T | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 9/10 | chr16 | 20315853 | |||||||
| chr16:20315859 | C | G | 44 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(41): Show |
115 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.1501+97G>C | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 9/10 | chr16 | 20315859 | |||||||
| chr16:20315879 | G | C | 1 | a0001c0001t0003g0071 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1501+77C>G | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 9/10 | chr16 | 20315879 | |||||||
| chr16:20316083 | C | G | 2 | a0001c0001t0001g0033 a0001c0001t0014g0090 |
3 | NA18978.hp2 NA19075.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.1417-43G>C | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 8/10 | chr16 | 20316083 | |||||||
| chr16:20316108 | C | T | 1 | a0001c0002t0002g0104 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1417-68G>A | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 8/10 | chr16 | 20316108 | |||||||
| chr16:20316152 | C | T | 1 | a0001c0001t0004g0053 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1417-112G>A | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 8/10 | chr16 | 20316152 | |||||||
| chr16:20316169 | C | T | 10 | a0001c0001t0007g0137 a0001c0005t0006g0044 a0001c0005t0006g0049 others(7): Show |
21 | HG01099.hp1 HG01175.hp1 HG01433.hp1 others(18): Show |
intron_variant | MODIFIER | c.1417-129G>A | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 8/10 | chr16 | 20316169 | |||||||
| chr16:20316176 | GT | G | 10 | a0001c0001t0007g0137 a0001c0005t0006g0044 a0001c0005t0006g0049 others(7): Show |
21 | HG01099.hp1 HG01175.hp1 HG01433.hp1 others(18): Show |
intron_variant | MODIFIER | c.1417-137delA | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 8/10 | chr16 | 20316176 | |||||||
| chr16:20316250 | T | A | 1 | a0001c0001t0001g0011 | 7 | NA18944.hp2 NA18955.hp2 NA18963.hp2 others(4): Show |
intron_variant | MODIFIER | c.1417-210A>T | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 8/10 | chr16 | 20316250 | |||||||
| chr16:20316425 | G | A | 1 | a0001c0001t0004g0058 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1417-385C>T | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 8/10 | chr16 | 20316425 | |||||||
| chr16:20316427 | A | T | 10 | a0001c0001t0007g0137 a0001c0005t0006g0044 a0001c0005t0006g0049 others(7): Show |
21 | HG01099.hp1 HG01175.hp1 HG01433.hp1 others(18): Show |
intron_variant | MODIFIER | c.1417-387T>A | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 8/10 | chr16 | 20316427 | |||||||
| chr16:20316444 | G | A | 1 | a0001c0001t0001g0099 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1417-404C>T | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 8/10 | chr16 | 20316444 | |||||||
| chr16:20316570 | A | G | 43 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(40): Show |
113 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.1417-530T>C | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 8/10 | chr16 | 20316570 | |||||||
| chr16:20316890 | C | T | 2 | a0001c0005t0006g0049 a0001c0005t0006g0163 |
3 | HG02895.hp2 HG02897.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1416+323G>A | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 8/10 | chr16 | 20316890 | |||||||
| chr16:20316935 | T | TCCCTTCC others(11): Show |
2 | a0001c0019t0003g0171 a0001c0020t0016g0158 |
2 | HG01934.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1416+260_1416+277d others(20): Show |
GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 8/10 | chr16 | 20316935 | |||||||
| chr16:20316949 | C | T | 31 | a0001c0002t0002g0003 a0001c0002t0002g0010 a0001c0002t0002g0016 others(28): Show |
67 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(64): Show |
intron_variant | MODIFIER | c.1416+264G>A | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 8/10 | chr16 | 20316949 | |||||||
| chr16:20316954 | T | C | 93 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(90): Show |
216 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1416+259A>G | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 8/10 | chr16 | 20316954 | |||||||
| chr16:20316963 | G | A | 1 | a0001c0001t0003g0135 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1416+250C>T | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 8/10 | chr16 | 20316963 | |||||||
| chr16:20317055 | C | A | 1 | a0001c0002t0002g0129 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1416+158G>T | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 8/10 | chr16 | 20317055 | |||||||
| chr16:20317089 | C | T | 1 | a0001c0001t0004g0061 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1416+124G>A | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 8/10 | chr16 | 20317089 | |||||||
| chr16:20317122 | G | A | 3 | a0001c0001t0004g0014 a0001c0001t0004g0030 a0001c0001t0004g0061 |
8 | NA18959.hp1 NA18968.hp1 NA18978.hp1 others(5): Show |
intron_variant | MODIFIER | c.1416+91C>T | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 8/10 | chr16 | 20317122 | |||||||
| chr16:20317384 | G | T | 1 | a0001c0001t0009g0152 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1254-9C>A | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 7/10 | chr16 | 20317384 | |||||||
| chr16:20317586 | C | T | 8 | a0001c0001t0007g0137 a0001c0005t0006g0044 a0001c0005t0006g0166 others(5): Show |
18 | HG01099.hp1 HG01175.hp1 HG01433.hp1 others(15): Show |
intron_variant | MODIFIER | c.1254-211G>A | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 7/10 | chr16 | 20317586 | |||||||
| chr16:20317626 | T | C | 42 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(39): Show |
112 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.1254-251A>G | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 7/10 | chr16 | 20317626 | |||||||
| chr16:20317963 | A | G | 3 | a0001c0001t0003g0067 a0001c0001t0003g0071 a0001c0001t0003g0162 |
3 | HG02280.hp2 HG02976.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1253+222T>C | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 7/10 | chr16 | 20317963 | |||||||
| chr16:20317980 | A | G | 1 | a0001c0001t0001g0032 | 2 | HG00408.hp2 HG00423.hp2 |
intron_variant | MODIFIER | c.1253+205T>C | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 7/10 | chr16 | 20317980 | |||||||
| chr16:20318180 | G | A | 1 | a0001c0002t0002g0108 | 1 | HG00099.hp2 | splice_region_variant&intron_variant | LOW | c.1253+5C>T | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 7/10 | chr16 | 20318180 | |||||||
| chr16:20318592 | C | T | 2 | a0001c0019t0003g0171 a0001c0020t0016g0158 |
2 | HG01934.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1008-162G>A | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 6/10 | chr16 | 20318592 | |||||||
| chr16:20318668 | G | A | 1 | a0001c0001t0001g0035 | 2 | NA18979.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.1008-238C>T | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 6/10 | chr16 | 20318668 | |||||||
| chr16:20318901 | T | C | 3 | a0001c0001t0003g0038 a0001c0001t0013g0114 a0001c0011t0013g0161 |
4 | HG01884.hp1 HG02622.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1008-471A>G | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 6/10 | chr16 | 20318901 | |||||||
| chr16:20319120 | G | A | 2 | a0001c0001t0001g0080 a0001c0001t0001g0100 |
2 | HG00609.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.1007+500C>T | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 6/10 | chr16 | 20319120 | |||||||
| chr16:20319154 | G | T | 82 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(79): Show |
193 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.1007+466C>A | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 6/10 | chr16 | 20319154 | |||||||
| chr16:20319219 | C | T | 79 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(76): Show |
190 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.1007+401G>A | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 6/10 | chr16 | 20319219 | |||||||
| chr16:20319444 | A | G | 1 | a0001c0001t0017g0085 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1007+176T>C | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 6/10 | chr16 | 20319444 | |||||||
| chr16:20319920 | G | C | 1 | a0001c0001t0010g0015 | 5 | HG00438.hp2 HG01934.hp1 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.859-152C>G | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 5/10 | chr16 | 20319920 | |||||||
| chr16:20319970 | T | C | 1 | a0001c0001t0003g0067 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.859-202A>G | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 5/10 | chr16 | 20319970 | |||||||
| chr16:20320065 | G | A | 98 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(95): Show |
233 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.858+197C>T | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 5/10 | chr16 | 20320065 | |||||||
| chr16:20320094 | C | T | 1 | a0001c0001t0004g0053 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.858+168G>A | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 5/10 | chr16 | 20320094 | |||||||
| chr16:20320096 | T | C | 1 | a0001c0001t0003g0067 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.858+166A>G | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 5/10 | chr16 | 20320096 | |||||||
| chr16:20320175 | G | A | 1 | a0001c0001t0001g0081 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.858+87C>T | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 5/10 | chr16 | 20320175 | |||||||
| chr16:20320176 | G | C | 78 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(75): Show |
189 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.858+86C>G | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 5/10 | chr16 | 20320176 | |||||||
| chr16:20320246 | T | G | 1 | a0001c0002t0005g0151 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.858+16A>C | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 5/10 | chr16 | 20320246 | |||||||
| chr16:20320625 | T | A | 1 | a0001c0011t0013g0161 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.647-152A>T | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 4/10 | chr16 | 20320625 | |||||||
| chr16:20320808 | A | G | 1 | a0001c0001t0009g0152 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.647-335T>C | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 4/10 | chr16 | 20320808 | |||||||
| chr16:20320878 | A | G | 91 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(88): Show |
208 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(205): Show |
intron_variant | MODIFIER | c.647-405T>C | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 4/10 | chr16 | 20320878 | |||||||
| chr16:20321051 | C | CT | 34 | a0001c0001t0001g0031 a0001c0001t0001g0107 a0001c0001t0003g0140 others(31): Show |
75 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(72): Show |
intron_variant | MODIFIER | c.647-579dupA | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 4/10 | chr16 | 20321051 | |||||||
| chr16:20321051 | CT | C | 25 | a0001c0001t0001g0082 a0001c0001t0001g0101 a0001c0001t0001g0102 others(22): Show |
51 | HG00558.hp1 HG00621.hp2 HG00642.hp2 others(48): Show |
intron_variant | MODIFIER | c.647-579delA | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 4/10 | chr16 | 20321051 | |||||||
| chr16:20321053 | T | C | 1 | a0001c0001t0004g0062 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.647-580A>G | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 4/10 | chr16 | 20321053 | |||||||
| chr16:20321180 | CTGGGATT others(7): Show |
C | 3 | a0001c0005t0006g0049 a0001c0005t0006g0163 a0001c0014t0005g0131 |
4 | HG01891.hp1 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.647-721_647-708del others(14): Show |
GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 4/10 | chr16 | 20321180 | |||||||
| chr16:20321195 | T | C | 41 | a0001c0001t0001g0107 a0001c0001t0002g0069 a0001c0001t0003g0018 others(38): Show |
83 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(80): Show |
intron_variant | MODIFIER | c.647-722A>G | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 4/10 | chr16 | 20321195 | |||||||
| chr16:20321287 | C | T | 1 | a0001c0001t0004g0053 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.647-814G>A | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 4/10 | chr16 | 20321287 | |||||||
| chr16:20321389 | A | G | 1 | a0001c0002t0005g0151 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.647-916T>C | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 4/10 | chr16 | 20321389 | |||||||
| chr16:20321467 | A | T | 2 | a0001c0019t0003g0171 a0001c0020t0016g0158 |
2 | HG01934.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.647-994T>A | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 4/10 | chr16 | 20321467 | |||||||
| chr16:20321511 | C | G | 1 | a0001c0003t0002g0124 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.647-1038G>C | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 4/10 | chr16 | 20321511 | |||||||
| chr16:20321775 | G | T | 10 | a0001c0001t0002g0069 a0001c0001t0003g0018 a0001c0001t0003g0067 others(7): Show |
16 | HG01496.hp1 HG02258.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.646+1094C>A | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 4/10 | chr16 | 20321775 | |||||||
| chr16:20321967 | C | A | 10 | a0001c0001t0002g0069 a0001c0001t0003g0018 a0001c0001t0003g0067 others(7): Show |
16 | HG01496.hp1 HG02258.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.646+902G>T | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 4/10 | chr16 | 20321967 | |||||||
| chr16:20321988 | T | C | 1 | a0001c0001t0003g0043 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.646+881A>G | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 4/10 | chr16 | 20321988 | |||||||
| chr16:20322064 | G | A | 1 | a0001c0002t0018g0172 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.646+805C>T | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 4/10 | chr16 | 20322064 | |||||||
| chr16:20322114 | G | A | 1 | a0001c0001t0001g0110 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.646+755C>T | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 4/10 | chr16 | 20322114 | |||||||
| chr16:20322231 | C | T | 1 | a0001c0002t0002g0084 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.646+638G>A | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 4/10 | chr16 | 20322231 | |||||||
| chr16:20322272 | G | T | 10 | a0001c0001t0002g0069 a0001c0001t0003g0018 a0001c0001t0003g0067 others(7): Show |
16 | HG01496.hp1 HG02258.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.646+597C>A | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 4/10 | chr16 | 20322272 | |||||||
| chr16:20322478 | G | C | 10 | a0001c0001t0002g0069 a0001c0001t0003g0018 a0001c0001t0003g0067 others(7): Show |
16 | HG01496.hp1 HG02258.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.646+391C>G | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 4/10 | chr16 | 20322478 | |||||||
| chr16:20322481 | T | C | 111 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(108): Show |
254 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.646+388A>G | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 4/10 | chr16 | 20322481 | |||||||
| chr16:20322661 | C | T | 1 | a0001c0002t0005g0151 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.646+208G>A | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 4/10 | chr16 | 20322661 | |||||||
| chr16:20323021 | C | T | 1 | a0001c0001t0003g0139 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.536-42G>A | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 3/10 | chr16 | 20323021 | |||||||
| chr16:20323357 | C | T | 107 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(104): Show |
249 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.536-378G>A | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 3/10 | chr16 | 20323357 | |||||||
| chr16:20323485 | A | AC | 23 | a0001c0001t0001g0007 a0001c0001t0001g0078 a0001c0001t0001g0080 others(20): Show |
43 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.535+330dupG | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 3/10 | chr16 | 20323485 | |||||||
| chr16:20323485 | A | T | 23 | a0001c0001t0002g0069 a0001c0001t0003g0018 a0001c0001t0003g0067 others(20): Show |
53 | HG00558.hp1 HG00621.hp2 HG01099.hp1 others(50): Show |
intron_variant | MODIFIER | c.535+331T>A | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 3/10 | chr16 | 20323485 | |||||||
| chr16:20323485 | AC | A | 36 | a0001c0001t0001g0112 a0001c0001t0001g0113 a0001c0001t0003g0002 others(33): Show |
69 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(66): Show |
intron_variant | MODIFIER | c.535+330delG | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 3/10 | chr16 | 20323485 | |||||||
| chr16:20323486 | C | A | 23 | a0001c0001t0002g0069 a0001c0001t0003g0018 a0001c0001t0003g0067 others(20): Show |
53 | HG00558.hp1 HG00621.hp2 HG01099.hp1 others(50): Show |
intron_variant | MODIFIER | c.535+330G>T | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 3/10 | chr16 | 20323486 | |||||||
| chr16:20323487 | C | T | 1 | a0001c0001t0005g0046 | 2 | HG02698.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.535+329G>A | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 3/10 | chr16 | 20323487 | |||||||
| chr16:20323489 | C | A | 1 | a0001c0001t0003g0148 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.535+327G>T | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 3/10 | chr16 | 20323489 | |||||||
| chr16:20323489 | C | G | 1 | a0001c0002t0002g0129 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.535+327G>C | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 3/10 | chr16 | 20323489 | |||||||
| chr16:20323489 | C | T | 1 | a0001c0002t0002g0040 | 2 | HG02165.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.535+327G>A | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 3/10 | chr16 | 20323489 | |||||||
| chr16:20323490 | C | G | 3 | a0001c0001t0002g0069 a0001c0001t0003g0018 a0001c0001t0003g0070 |
6 | HG01496.hp1 HG02258.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.535+326G>C | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 3/10 | chr16 | 20323490 | |||||||
| chr16:20323494 | C | G | 16 | a0001c0001t0004g0057 a0001c0001t0005g0046 a0001c0005t0002g0068 others(13): Show |
40 | HG00558.hp1 HG00621.hp2 HG01099.hp1 others(37): Show |
intron_variant | MODIFIER | c.535+322G>C | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 3/10 | chr16 | 20323494 | |||||||
| chr16:20323495 | C | G | 1 | a0001c0001t0003g0135 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.535+321G>C | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 3/10 | chr16 | 20323495 | |||||||
| chr16:20323563 | G | A | 2 | a0001c0001t0001g0119 a0001c0001t0011g0118 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.535+253C>T | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 3/10 | chr16 | 20323563 | |||||||
| chr16:20323595 | A | C | 2 | a0001c0001t0003g0045 a0001c0001t0003g0149 |
3 | HG01891.hp2 HG02257.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.535+221T>G | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 3/10 | chr16 | 20323595 | |||||||
| chr16:20323610 | G | A | 168 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(165): Show |
380 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(377): Show |
intron_variant | MODIFIER | c.535+206C>T | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 3/10 | chr16 | 20323610 | |||||||
| chr16:20323657 | G | C | 2 | a0001c0001t0001g0039 a0001c0001t0021g0120 |
3 | HG02027.hp2 NA18747.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.535+159C>G | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 3/10 | chr16 | 20323657 | |||||||
| chr16:20323680 | C | T | 1 | a0001c0001t0003g0134 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.535+136G>A | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 3/10 | chr16 | 20323680 | |||||||
| chr16:20323706 | C | T | 2 | a0001c0001t0003g0133 a0001c0001t0022g0132 |
2 | HG02723.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.535+110G>A | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 3/10 | chr16 | 20323706 | |||||||
| chr16:20323730 | C | T | 10 | a0001c0001t0002g0069 a0001c0001t0003g0018 a0001c0001t0003g0067 others(7): Show |
16 | HG01496.hp1 HG02258.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.535+86G>A | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 3/10 | chr16 | 20323730 | |||||||
| chr16:20323757 | G | A | 2 | a0001c0019t0003g0171 a0001c0020t0016g0158 |
2 | HG01934.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.535+59C>T | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 3/10 | chr16 | 20323757 | |||||||
| chr16:20324357 | A | G | 1 | a0001c0001t0004g0053 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.95-101T>C | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 2/10 | chr16 | 20324357 | |||||||
| chr16:20324378 | T | A | 1 | a0001c0005t0002g0068 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.95-122A>T | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 2/10 | chr16 | 20324378 | |||||||
| chr16:20324464 | T | G | 27 | a0001c0001t0003g0002 a0001c0001t0003g0006 a0001c0001t0003g0012 others(24): Show |
65 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(62): Show |
intron_variant | MODIFIER | c.95-208A>C | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 2/10 | chr16 | 20324464 | |||||||
| chr16:20324474 | C | G | 1 | a0001c0001t0004g0052 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.95-218G>C | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 2/10 | chr16 | 20324474 | |||||||
| chr16:20324535 | A | C | 146 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(143): Show |
329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.95-279T>G | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 2/10 | chr16 | 20324535 | |||||||
| chr16:20324706 | G | A | 1 | a0001c0001t0014g0128 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.95-450C>T | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 2/10 | chr16 | 20324706 | |||||||
| chr16:20324814 | C | T | 1 | a0001c0005t0002g0068 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.95-558G>A | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 2/10 | chr16 | 20324814 | |||||||
| chr16:20324851 | C | G | 2 | a0001c0001t0005g0046 a0001c0009t0005g0047 |
4 | HG01109.hp1 HG02698.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.95-595G>C | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 2/10 | chr16 | 20324851 | |||||||
| chr16:20324872 | G | A | 10 | a0001c0001t0002g0069 a0001c0001t0003g0018 a0001c0001t0003g0067 others(7): Show |
16 | HG01496.hp1 HG02257.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.95-616C>T | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 2/10 | chr16 | 20324872 | |||||||
| chr16:20324872 | G | T | 1 | a0001c0001t0003g0130 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.95-616C>A | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 2/10 | chr16 | 20324872 | |||||||
| chr16:20324935 | A | G | 57 | a0001c0001t0002g0069 a0001c0001t0003g0002 a0001c0001t0003g0006 others(54): Show |
126 | HG00099.hp1 HG00140.hp2 HG00558.hp1 others(123): Show |
intron_variant | MODIFIER | c.95-679T>C | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 2/10 | chr16 | 20324935 | |||||||
| chr16:20325000 | T | C | 4 | a0001c0002t0002g0016 a0001c0002t0002g0040 a0001c0002t0002g0041 others(1): Show |
10 | HG00438.hp1 HG00597.hp2 HG02027.hp1 others(7): Show |
intron_variant | MODIFIER | c.95-744A>G | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 2/10 | chr16 | 20325000 | |||||||
| chr16:20325057 | T | C | 1 | a0001c0001t0009g0159 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.95-801A>G | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 2/10 | chr16 | 20325057 | |||||||
| chr16:20325269 | C | T | 111 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(108): Show |
254 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.95-1013G>A | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 2/10 | chr16 | 20325269 | |||||||
| chr16:20325506 | C | T | 10 | a0001c0001t0002g0069 a0001c0001t0003g0018 a0001c0001t0003g0067 others(7): Show |
16 | HG01496.hp1 HG02257.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.94+832G>A | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 2/10 | chr16 | 20325506 | |||||||
| chr16:20325660 | G | A | 1 | a0001c0002t0018g0172 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.94+678C>T | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 2/10 | chr16 | 20325660 | |||||||
| chr16:20325792 | C | T | 1 | a0001c0001t0005g0046 | 2 | HG02698.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.94+546G>A | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 2/10 | chr16 | 20325792 | |||||||
| chr16:20325797 | A | G | 2 | a0001c0001t0003g0067 a0001c0002t0018g0172 |
2 | HG02280.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.94+541T>C | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 2/10 | chr16 | 20325797 | |||||||
| chr16:20325864 | C | T | 16 | a0001c0001t0003g0162 a0001c0005t0002g0169 a0001c0005t0006g0049 others(13): Show |
39 | HG00558.hp1 HG00621.hp2 HG01099.hp1 others(36): Show |
intron_variant | MODIFIER | c.94+474G>A | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 2/10 | chr16 | 20325864 | |||||||
| chr16:20326092 | T | C | 1 | a0001c0001t0004g0065 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.94+246A>G | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 2/10 | chr16 | 20326092 | |||||||
| chr16:20326207 | C | T | 1 | a0001c0002t0002g0076 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.94+131G>A | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 2/10 | chr16 | 20326207 | |||||||
| chr16:20326211 | T | C | 1 | a0001c0001t0001g0157 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.94+127A>G | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 2/10 | chr16 | 20326211 | |||||||
| chr16:20326562 | T | C | 16 | a0001c0001t0003g0162 a0001c0005t0002g0169 a0001c0005t0006g0049 others(13): Show |
39 | HG00558.hp1 HG00621.hp2 HG01099.hp1 others(36): Show |
intron_variant | MODIFIER | c.-36-95A>G | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 1/10 | chr16 | 20326562 | |||||||
| chr16:20326581 | T | C | 1 | a0001c0001t0004g0066 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-36-114A>G | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 1/10 | chr16 | 20326581 | |||||||
| chr16:20326707 | T | C | 1 | a0001c0020t0016g0158 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-36-240A>G | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 1/10 | chr16 | 20326707 | |||||||
| chr16:20326789 | C | T | 10 | a0001c0001t0002g0069 a0001c0001t0003g0018 a0001c0001t0003g0067 others(7): Show |
16 | HG01496.hp1 HG02257.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.-36-322G>A | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 1/10 | chr16 | 20326789 | |||||||
| chr16:20326883 | T | C | 150 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(147): Show |
335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.-36-416A>G | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 1/10 | chr16 | 20326883 | |||||||
| chr16:20326886 | T | C | 1 | a0001c0001t0009g0159 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-36-419A>G | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 1/10 | chr16 | 20326886 | |||||||
| chr16:20326985 | G | A | 2 | a0001c0001t0005g0046 a0001c0009t0005g0047 |
4 | HG01109.hp1 HG02698.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.-37+482C>T | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 1/10 | chr16 | 20326985 | |||||||
| chr16:20326998 | G | T | 1 | a0001c0002t0018g0172 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-37+469C>A | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 1/10 | chr16 | 20326998 | |||||||
| chr16:20327121 | C | T | 1 | a0001c0001t0003g0051 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-37+346G>A | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 1/10 | chr16 | 20327121 | |||||||
| chr16:20327128 | G | A | 4 | a0001c0003t0002g0021 a0001c0003t0002g0027 a0001c0003t0002g0160 others(1): Show |
9 | HG01071.hp1 HG01167.hp1 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.-37+339C>T | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 1/10 | chr16 | 20327128 | |||||||
| chr16:20327207 | C | A | 1 | a0001c0001t0009g0048 | 2 | HG02258.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.-37+260G>T | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 1/10 | chr16 | 20327207 | |||||||
| chr16:20327240 | C | G | 1 | a0001c0001t0004g0050 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.-37+227G>C | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 1/10 | chr16 | 20327240 | |||||||
| chr16:20327288 | G | A | 16 | a0001c0001t0003g0162 a0001c0005t0002g0169 a0001c0005t0006g0049 others(13): Show |
39 | HG00558.hp1 HG00621.hp2 HG01099.hp1 others(36): Show |
intron_variant | MODIFIER | c.-37+179C>T | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 1/10 | chr16 | 20327288 | |||||||
| chr16:20327300 | G | A | 16 | a0001c0001t0003g0162 a0001c0005t0002g0169 a0001c0005t0006g0049 others(13): Show |
39 | HG00558.hp1 HG00621.hp2 HG01099.hp1 others(36): Show |
intron_variant | MODIFIER | c.-37+167C>T | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 1/10 | chr16 | 20327300 | |||||||
| chr16:20327377 | T | G | 1 | a0001c0002t0018g0172 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-37+90A>C | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 1/10 | chr16 | 20327377 | |||||||
| chr16:20327405 | C | A | 1 | a0001c0003t0002g0173 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.-37+62G>T | GP2 | ENSG00000169347.17 | transcript | ENST00000302555.10 | protein_coding | 1/10 | chr16 | 20327405 |