Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 84572 |
| ensemblid | ENSG00000090581.11 |
| hgncid | 23026 |
| symbol | GNPTG |
| name | N-acetylglucosamine-1-phosphate transferase subunit gamma |
| refseq_nuc | NM_032520.5 |
| refseq_prot | NP_115909.1 |
| ensembl_nuc | ENST00000204679.9 |
| ensembl_prot | ENSP00000204679.4 |
| mane_status | MANE Select |
| chr | chr16 |
| start | 1351931 |
| end | 1364113 |
| strand | + |
| ver | v1.2 |
| region | chr16:1351931-1364113 |
| region5000 | chr16:1346931-1369113 |
| regionname0 | GNPTG_chr16_1351931_1364113 |
| regionname5000 | GNPTG_chr16_1346931_1369113 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 305 | 372 | 91 | 72 | 143 | 18 | 46 | 97 | GNPTG_chr16_1346931_1369113 | GNPTG | MAAGL others(300): Show |
chr16 | 1346931 | 1369113 |
| a0002 | 0/0 | 305 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | GNPTG_chr16_1346931_1369113 | GNPTG | MAAAL others(300): Show |
chr16 | 1346931 | 1369113 |
| a0003 | 0/0 | 305 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | MAAGL others(300): Show |
chr16 | 1346931 | 1369113 |
| a0004 | 0/0 | 59 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | MAAGL others(54): Show |
chr16 | 1346931 | 1369113 |
| a0005 | 0/0 | 305 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | MATGL others(300): Show |
chr16 | 1346931 | 1369113 |
| a0006 | 0/0 | 305 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GNPTG_chr16_1346931_1369113 | GNPTG | MAAGL others(300): Show |
chr16 | 1346931 | 1369113 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 915 | 369 | 88 | 72 | 143 | 18 | 46 | GNPTG_chr16_1346931_1369113 | GNPTG | ATGGC others(910): Show |
chr16 | 1346931 | 1369113 | ||
| a0001c0002 | 0/0 | 915 | 3 | 3 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | ATGGC others(910): Show |
chr16 | 1346931 | 1369113 | ||
| a0002c0003 | 0/0 | 915 | 2 | 0 | 0 | 2 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | ATGGC others(910): Show |
chr16 | 1346931 | 1369113 | ||
| a0003c0005 | 0/0 | 915 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | ATGGC others(910): Show |
chr16 | 1346931 | 1369113 | ||
| a0004c0006 | 0/0 | 178 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | ATGGC others(173): Show |
chr16 | 1346931 | 1369113 | ||
| a0005c0004 | 0/0 | 915 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | ATGGC others(910): Show |
chr16 | 1346931 | 1369113 | ||
| a0006c0007 | 0/0 | 915 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | ATGGC others(910): Show |
chr16 | 1346931 | 1369113 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 1975 | 367 | 88 | 72 | 143 | 18 | 45 | GNPTG_chr16_1346931_1369113 | GNPTG | ACTTC others(1970): Show |
chr16 | 1346931 | 1369113 |
| a0001c0001t0003 | 0/1 | 1975 | 1 | 0 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | ACTTC others(1970): Show |
chr16 | 1346931 | 1369113 |
| a0001c0001t0004 | 0/0 | 1975 | 1 | 0 | 0 | 0 | 0 | 1 | GNPTG_chr16_1346931_1369113 | GNPTG | ACTTC others(1970): Show |
chr16 | 1346931 | 1369113 |
| a0001c0002t0001 | 0/0 | 1975 | 3 | 3 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | ACTTC others(1970): Show |
chr16 | 1346931 | 1369113 |
| a0002c0003t0001 | 0/0 | 1975 | 2 | 0 | 0 | 2 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | ACTTC others(1970): Show |
chr16 | 1346931 | 1369113 |
| a0003c0005t0001 | 0/0 | 1975 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | ACTTC others(1970): Show |
chr16 | 1346931 | 1369113 |
| a0004c0006t0002 | 0/0 | 213 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | ACTTC others(208): Show |
chr16 | 1346931 | 1369113 |
| a0005c0004t0001 | 0/0 | 1975 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | ACTTC others(1970): Show |
chr16 | 1346931 | 1369113 |
| a0006c0007t0001 | 0/0 | 1975 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | ACTTC others(1970): Show |
chr16 | 1346931 | 1369113 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 56 | 4 | 24 | 19 | 2 | 7 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| a0001c0001t0001g0002 | 0/0 | 34 | 1 | 3 | 25 | 2 | 3 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| a0001c0001t0001g0003 | 0/0 | 24 | 6 | 4 | 5 | 3 | 6 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| a0001c0001t0001g0004 | 0/0 | 20 | 0 | 2 | 16 | 1 | 1 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| a0001c0001t0001g0005 | 0/0 | 16 | 2 | 5 | 7 | 0 | 2 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| a0001c0001t0001g0006 | 0/0 | 16 | 0 | 1 | 14 | 0 | 1 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| a0001c0001t0001g0007 | 0/0 | 17 | 5 | 5 | 1 | 3 | 3 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| a0001c0001t0001g0008 | 0/0 | 12 | 4 | 0 | 7 | 0 | 1 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| a0001c0001t0001g0009 | 1/0 | 9 | 2 | 3 | 0 | 0 | 3 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| a0001c0001t0001g0010 | 0/0 | 9 | 0 | 1 | 6 | 0 | 2 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| a0001c0001t0001g0011 | 0/0 | 9 | 8 | 1 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| a0001c0001t0001g0012 | 0/0 | 7 | 3 | 1 | 3 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| a0001c0001t0001g0013 | 0/0 | 7 | 5 | 2 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| a0001c0001t0001g0014 | 0/0 | 6 | 5 | 1 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| a0001c0001t0001g0015 | 0/0 | 5 | 0 | 1 | 3 | 1 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| a0001c0001t0001g0016 | 0/0 | 5 | 1 | 1 | 1 | 0 | 2 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| a0001c0001t0001g0017 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| a0001c0001t0001g0018 | 0/0 | 4 | 1 | 0 | 0 | 0 | 3 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| a0001c0001t0001g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| a0001c0001t0001g0020 | 0/0 | 3 | 2 | 0 | 0 | 0 | 1 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| a0001c0001t0001g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| a0001c0001t0001g0022 | 0/0 | 3 | 2 | 0 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| a0001c0001t0001g0023 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| a0001c0001t0001g0024 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| a0001c0001t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| a0001c0001t0001g0030 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| a0001c0001t0001g0033 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| a0001c0001t0001g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| a0001c0001t0001g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| a0001c0001t0001g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| a0001c0001t0003g0077 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| a0001c0001t0004g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| a0001c0002t0001g0005 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| a0002c0003t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| a0003c0005t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| a0004c0006t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| a0005c0004t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| a0006c0007t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0075 | EUR | GBR | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | GBR | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | GBR | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | GBR | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0015 | EUR | FIN | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | FIN | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0007 | EUR | FIN | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | CHS | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | CHS | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | CHS | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | CHS | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | PUR | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0059 | AMR | PUR | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | PUR | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | PUR | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0049 | AMR | CLM | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0053 | AMR | CLM | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0007 | EUR | IBS | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0060 | EUR | IBS | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0045 | EUR | IBS | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0088 | EUR | IBS | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0007 | EUR | IBS | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | ACB | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG01884 | hp2 | a0001 | c0002 | t0001 | g0005 | AFR | ACB | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG01891 | hp1 | a0001 | c0002 | t0001 | g0005 | AFR | ACB | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | PEL | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | PEL | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PEL | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PEL | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PEL | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | ACB | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | KHV | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | KHV | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | KHV | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | KHV | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | KHV | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | CDX | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CDX | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | ACB | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | ACB | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | ACB | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | KHV | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | GWD | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | GWD | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG02630 | hp2 | a0003 | c0005 | t0001 | g0103 | AFR | GWD | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0018 | SAS | PJL | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | GWD | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0046 | SAS | PJL | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | GWD | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | GWD | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | GWD | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG02922 | hp1 | a0004 | c0006 | t0002 | g0042 | AFR | ESN | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG02922 | hp2 | a0005 | c0004 | t0001 | g0091 | AFR | ESN | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | ESN | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | ESN | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | ESN | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | ESN | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0086 | SAS | PJL | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | GWD | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | MSL | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | MSL | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | MSL | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | MSL | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0065 | SAS | PJL | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG03239 | hp2 | a0001 | c0001 | t0004 | g0031 | SAS | PJL | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | MSL | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | MSL | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | MSL | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0048 | SAS | PJL | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | ESN | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | MSL | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | MSL | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0079 | SAS | PJL | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | STU | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0018 | SAS | PJL | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0076 | SAS | BEB | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | BEB | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0070 | SAS | BEB | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0018 | SAS | BEB | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | STU | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | STU | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0080 | SAS | BEB | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0020 | SAS | BEB | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | STU | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | STU | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0016 | SAS | STU | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | YRI | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | YRI | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | CHB | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CHB | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHB | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | YRI | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | YRI | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| NA18939 | hp1 | a0002 | c0003 | t0001 | g0006 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| NA18962 | hp1 | a0002 | c0003 | t0001 | g0006 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | LWK | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | LWK | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | LWK | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| NA19043 | hp2 | a0001 | c0002 | t0001 | g0005 | AFR | LWK | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| NA19059 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| NA19059 | hp2 | a0006 | c0007 | t0001 | g0083 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | YRI | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | YRI | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | ASW | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | ASW | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0067 | EUR | TSI | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | TSI | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0062 | EUR | TSI | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0081 | SAS | GIH | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | GIH | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | ACB | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | ACB | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | MSL | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | USA | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | USA | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | USA | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | USA | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | LWK | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0003 | g0077 | REF | REF | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0009 | REF | REF | GNPTG_chr16_1346931_1369113 | GNPTG | chr16 | 1346931 | 1369113 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:1351972 | G | A | 1 | a0005 | 1 | HG02922.hp2 | missense_variant | MODERATE | c.7G>A | p.Ala3Thr | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 1/11 | 42/1975 | 7/918 | 3/305 | chr16 | 1351972 | |||
| chr16:1351976 | G | C | 1 | a0002 | 2 | NA18939.hp1 NA18962.hp1 |
missense_variant | MODERATE | c.11G>C | p.Gly4Ala | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 1/11 | 46/1975 | 11/918 | 4/305 | chr16 | 1351976 | |||
| chr16:1352132 | A | C | 1 | a0006 | 1 | NA19059.hp2 | missense_variant | MODERATE | c.83A>C | p.Lys28Thr | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 2/11 | 118/1975 | 83/918 | 28/305 | chr16 | 1352132 | |||
| chr16:1352241 | T | C | 1 | a0003 | 1 | HG02630.hp2 | missense_variant&splice_region_variant | MODERATE | c.113T>C | p.Val38Ala | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/11 | 148/1975 | 113/918 | 38/305 | chr16 | 1352241 | |||
| chr16:1356771 | GTCTCCAA others(8137): Show |
G | 1 | a0004 | 1 | HG02922.hp1 | exon_loss_variant | HIGH | c.178+4467_*1825del | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr16 | 1356771 | ||||||
| chr16:1362244 | T | G | 1 | a0001 | 1 | NA20129.hp2 | missense_variant | MODERATE | c.450T>G | p.His150Gln | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 7/11 | 485/1975 | 450/918 | 150/305 | chr16 | 1362244 | |||
| chr16:1362482 | G | A | 1 | a0001 | 1 | HG01109.hp2 | missense_variant | MODERATE | c.557G>A | p.Arg186Gln | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 8/11 | 592/1975 | 557/918 | 186/305 | chr16 | 1362482 | |||
| chr16:1362897 | A | G | 1 | a0001 | 1 | NA19030.hp2 | missense_variant | MODERATE | c.814A>G | p.Arg272Gly | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 10/11 | 849/1975 | 814/918 | 272/305 | chr16 | 1362897 | |||
| chr16:1363083 | A | G | 1 | a0001 | 1 | HG02723.hp1 | missense_variant | MODERATE | c.910A>G | p.Ser304Gly | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 11/11 | 945/1975 | 910/918 | 304/305 | chr16 | 1363083 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:1351993 | T | C | 1 | a0001c0002 | 3 | HG01884.hp2 HG01891.hp1 NA19043.hp2 |
synonymous_variant | LOW | c.28T>C | p.Leu10Leu | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 1/11 | 63/1975 | 28/918 | 10/305 | chr16 | 1351993 | |||
| chr16:1361893 | G | A | 1 | a0001c0001 | 1 | HG00099.hp2 | synonymous_variant | LOW | c.255G>A | p.Pro85Pro | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 5/11 | 290/1975 | 255/918 | 85/305 | chr16 | 1361893 | |||
| chr16:1362271 | C | T | 1 | a0001c0001 | 1 | NA20129.hp1 | synonymous_variant | LOW | c.477C>T | p.Tyr159Tyr | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 7/11 | 512/1975 | 477/918 | 159/305 | chr16 | 1362271 | |||
| chr16:1362528 | C | T | 1 | a0001c0001 | 2 | HG03209.hp1 HG03225.hp2 |
synonymous_variant | LOW | c.603C>T | p.Thr201Thr | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 8/11 | 638/1975 | 603/918 | 201/305 | chr16 | 1362528 | |||
| chr16:1362703 | T | C | 1 | a0001c0001 | 1 | HG03834.hp1 | synonymous_variant | LOW | c.702T>C | p.Pro234Pro | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 9/11 | 737/1975 | 702/918 | 234/305 | chr16 | 1362703 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:1351962 | C | T | 1 | a0001c0001t0004 | 1 | HG03239.hp2 | 5_prime_UTR_variant | MODIFIER | c.-4C>T | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 1/11 | 4 | chr16 | 1351962 | ||||||
| chr16:1363118 | C | T | 1 | a0001c0001t0001 | 1 | HG00544.hp2 | 3_prime_UTR_variant | MODIFIER | c.*27C>T | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 11/11 | 27 | chr16 | 1363118 | ||||||
| chr16:1363159 | G | T | 1 | a0001c0001t0001 | 3 | HG02559.hp2 HG02896.hp2 NA18943.hp2 |
3_prime_UTR_variant | MODIFIER | c.*68G>T | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 11/11 | 68 | chr16 | 1363159 | ||||||
| chr16:1363177 | G | T | 1 | a0006c0007t0001 | 1 | NA19059.hp2 | 3_prime_UTR_variant | MODIFIER | c.*86G>T | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 11/11 | 86 | chr16 | 1363177 | ||||||
| chr16:1363315 | T | C | 1 | a0001c0001t0001 | 6 | HG00639.hp1 HG02622.hp1 HG02647.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*224T>C | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 11/11 | 224 | chr16 | 1363315 | ||||||
| chr16:1363426 | G | A | 2 | a0001c0001t0001 a0001c0002t0001 |
26 | HG00099.hp1 HG00423.hp2 HG00609.hp2 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*335G>A | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 11/11 | 335 | chr16 | 1363426 | ||||||
| chr16:1363556 | G | A | 1 | a0001c0001t0001 | 1 | HG02896.hp1 | 3_prime_UTR_variant | MODIFIER | c.*465G>A | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 11/11 | 465 | chr16 | 1363556 | ||||||
| chr16:1363638 | T | C | 1 | a0001c0001t0001 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*547T>C | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 11/11 | 547 | chr16 | 1363638 | ||||||
| chr16:1363644 | G | A | 1 | a0001c0001t0001 | 1 | NA18906.hp2 | 3_prime_UTR_variant | MODIFIER | c.*553G>A | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 11/11 | 553 | chr16 | 1363644 | ||||||
| chr16:1363695 | G | A | 1 | a0001c0001t0001 | 3 | HG02630.hp1 HG03225.hp1 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*604G>A | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 11/11 | 604 | chr16 | 1363695 | ||||||
| chr16:1363815 | C | T | 1 | a0001c0001t0001 | 1 | NA19087.hp1 | 3_prime_UTR_variant | MODIFIER | c.*724C>T | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 11/11 | 724 | chr16 | 1363815 | ||||||
| chr16:1363905 | C | T | 1 | a0001c0001t0001 | 3 | HG02572.hp2 HG02818.hp1 HG02896.hp1 |
3_prime_UTR_variant | MODIFIER | c.*814C>T | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 11/11 | 814 | chr16 | 1363905 | ||||||
| chr16:1363920 | G | C | 1 | a0001c0001t0001 | 3 | HG02630.hp1 HG03225.hp1 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*829G>C | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 11/11 | 829 | chr16 | 1363920 | ||||||
| chr16:1363942 | G | A | 1 | a0001c0001t0001 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*851G>A | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 11/11 | 851 | chr16 | 1363942 | ||||||
| chr16:1364012 | CGGGAGAT others(25): Show |
C | 1 | a0001c0001t0001 | 1 | HG02273.hp1 | 3_prime_UTR_variant | MODIFIER | c.*923_*954delGGAGAT others(26): Show |
GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 11/11 | 923 | INFO_REALIGN_3_PRIME | chr16 | 1364012 | |||||
| chr16:1364013 | G | A | 1 | a0001c0001t0001 | 1 | HG00673.hp2 | 3_prime_UTR_variant | MODIFIER | c.*922G>A | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 11/11 | 922 | chr16 | 1364013 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:1352386 | G | A | 1 | a0001c0001t0001g0041 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.178+80G>A | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1352386 | |||||||
| chr16:1352424 | C | T | 1 | a0003c0005t0001g0103 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.178+118C>T | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1352424 | |||||||
| chr16:1352492 | C | T | 8 | a0001c0001t0001g0011 a0001c0001t0001g0023 a0001c0001t0001g0024 others(5): Show |
22 | HG01099.hp1 HG02109.hp1 HG02280.hp2 others(19): Show |
intron_variant | MODIFIER | c.178+186C>T | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1352492 | |||||||
| chr16:1352630 | T | A | 1 | a0001c0001t0001g0096 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.178+324T>A | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1352630 | |||||||
| chr16:1352712 | T | C | 2 | a0001c0001t0001g0019 a0004c0006t0002g0042 |
4 | HG02257.hp1 HG02922.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.178+406T>C | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1352712 | |||||||
| chr16:1352753 | A | T | 2 | a0001c0001t0001g0038 a0001c0001t0001g0099 |
3 | NA18953.hp2 NA18962.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.178+447A>T | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1352753 | |||||||
| chr16:1352915 | A | G | 1 | a0001c0001t0001g0098 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.178+609A>G | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1352915 | |||||||
| chr16:1352967 | A | AT | 67 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(64): Show |
302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.178+680dupT | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 1352967 | ||||||
| chr16:1352967 | A | ATT | 23 | a0001c0001t0001g0007 a0001c0001t0001g0018 a0001c0001t0001g0022 others(20): Show |
48 | HG00323.hp2 HG00639.hp2 HG00738.hp2 others(45): Show |
intron_variant | MODIFIER | c.178+679_178+680dup others(2): Show |
GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 1352967 | ||||||
| chr16:1352967 | ATT | A | 4 | a0001c0001t0001g0023 a0001c0001t0001g0039 a0001c0001t0001g0100 others(1): Show |
7 | HG02451.hp1 HG02486.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.178+679_178+680del others(2): Show |
GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 1352967 | ||||||
| chr16:1353253 | A | G | 3 | a0001c0001t0001g0082 a0001c0001t0001g0096 a0001c0001t0001g0097 |
3 | HG02818.hp2 HG02896.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.178+947A>G | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1353253 | |||||||
| chr16:1353267 | G | A | 1 | a0001c0001t0001g0052 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.178+961G>A | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1353267 | |||||||
| chr16:1353332 | G | A | 1 | a0001c0001t0001g0043 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.178+1026G>A | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1353332 | |||||||
| chr16:1353549 | G | A | 1 | a0006c0007t0001g0083 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.178+1243G>A | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1353549 | |||||||
| chr16:1353597 | C | T | 89 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(86): Show |
347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): Show |
intron_variant | MODIFIER | c.178+1291C>T | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1353597 | |||||||
| chr16:1353613 | T | C | 1 | a0001c0001t0001g0082 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.178+1307T>C | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1353613 | |||||||
| chr16:1353664 | C | T | 1 | a0001c0001t0001g0045 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.178+1358C>T | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1353664 | |||||||
| chr16:1353725 | A | G | 2 | a0001c0001t0001g0019 a0004c0006t0002g0042 |
4 | HG02257.hp1 HG02922.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.178+1419A>G | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1353725 | |||||||
| chr16:1353997 | G | A | 1 | a0001c0001t0001g0084 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.178+1691G>A | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1353997 | |||||||
| chr16:1354122 | G | A | 1 | a0001c0001t0001g0054 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.178+1816G>A | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1354122 | |||||||
| chr16:1354192 | CTG | C | 97 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(94): Show |
358 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(355): Show |
intron_variant | MODIFIER | c.178+1890_178+1891d others(4): Show |
GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 1354192 | ||||||
| chr16:1354268 | T | C | 2 | a0001c0001t0001g0019 a0004c0006t0002g0042 |
4 | HG02257.hp1 HG02922.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.178+1962T>C | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1354268 | |||||||
| chr16:1354321 | G | A | 2 | a0001c0001t0001g0027 a0001c0001t0001g0055 |
3 | HG01943.hp1 HG02004.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.178+2015G>A | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1354321 | |||||||
| chr16:1354325 | A | G | 2 | a0001c0001t0001g0079 a0001c0001t0001g0080 |
2 | HG03669.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.178+2019A>G | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1354325 | |||||||
| chr16:1354380 | A | C | 1 | a0001c0001t0001g0013 | 7 | HG01069.hp2 HG01071.hp2 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.178+2074A>C | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1354380 | |||||||
| chr16:1354416 | A | G | 1 | a0001c0001t0001g0078 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.178+2110A>G | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1354416 | |||||||
| chr16:1354585 | C | CA | 16 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0015 others(13): Show |
95 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.178+2303dupA | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 1354585 | ||||||
| chr16:1354585 | C | CAA | 12 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0022 others(9): Show |
47 | HG00140.hp1 HG00140.hp2 HG00733.hp2 others(44): Show |
intron_variant | MODIFIER | c.178+2302_178+2303d others(4): Show |
GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 1354585 | ||||||
| chr16:1354585 | C | CAAA | 5 | a0001c0001t0001g0012 a0001c0001t0001g0024 a0001c0001t0001g0037 others(2): Show |
14 | HG00735.hp2 HG02486.hp2 HG02523.hp2 others(11): Show |
intron_variant | MODIFIER | c.178+2301_178+2303d others(5): Show |
GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 1354585 | ||||||
| chr16:1354585 | C | CAAAAAAA others(3): Show |
1 | a0001c0001t0001g0090 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.178+2294_178+2303d others(12): Show |
GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 1354585 | ||||||
| chr16:1354585 | C | CAAAAAAA others(4): Show |
5 | a0001c0001t0001g0017 a0001c0001t0001g0066 a0001c0001t0001g0078 others(2): Show |
8 | HG00639.hp1 HG02622.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.178+2293_178+2303d others(13): Show |
GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 1354585 | ||||||
| chr16:1354585 | C | CAAAAAAA others(5): Show |
6 | a0001c0001t0001g0031 a0001c0001t0001g0039 a0001c0001t0001g0064 others(3): Show |
7 | HG00738.hp1 HG02451.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.178+2292_178+2303d others(14): Show |
GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 1354585 | ||||||
| chr16:1354585 | C | CAAAAAAA others(6): Show |
7 | a0001c0001t0001g0006 a0001c0001t0001g0030 a0001c0001t0001g0036 others(4): Show |
25 | HG00408.hp1 HG00544.hp2 HG00621.hp1 others(22): Show |
intron_variant | MODIFIER | c.178+2291_178+2303d others(15): Show |
GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 1354585 | ||||||
| chr16:1354585 | C | CAAAAAAA others(7): Show |
9 | a0001c0001t0001g0002 a0001c0001t0001g0027 a0001c0001t0001g0035 others(6): Show |
44 | HG00280.hp2 HG00597.hp2 HG00673.hp2 others(41): Show |
intron_variant | MODIFIER | c.178+2290_178+2303d others(16): Show |
GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 1354585 | ||||||
| chr16:1354585 | C | CAAAAAAA others(8): Show |
6 | a0001c0001t0001g0004 a0001c0001t0001g0034 a0001c0001t0001g0055 others(3): Show |
26 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(23): Show |
intron_variant | MODIFIER | c.178+2289_178+2303d others(17): Show |
GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 1354585 | ||||||
| chr16:1354585 | C | CAAAAAAA others(9): Show |
2 | a0001c0001t0001g0010 a0001c0001t0001g0047 |
10 | HG00544.hp1 HG00558.hp1 HG00733.hp1 others(7): Show |
intron_variant | MODIFIER | c.178+2288_178+2303d others(18): Show |
GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 1354585 | ||||||
| chr16:1354585 | C | CAAAAAAA others(10): Show |
6 | a0001c0001t0001g0029 a0001c0001t0001g0041 a0001c0001t0001g0046 others(3): Show |
7 | HG02738.hp1 HG02970.hp1 HG03486.hp2 others(4): Show |
intron_variant | MODIFIER | c.178+2287_178+2303d others(19): Show |
GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 1354585 | ||||||
| chr16:1354585 | C | CAAAAAAA others(11): Show |
1 | a0001c0001t0001g0057 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.178+2286_178+2303d others(20): Show |
GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 1354585 | ||||||
| chr16:1354585 | C | CAAAAAAA others(13): Show |
1 | a0001c0001t0001g0028 | 2 | HG03654.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.178+2284_178+2303d others(22): Show |
GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 1354585 | ||||||
| chr16:1354585 | C | CAAAAAAA others(14): Show |
1 | a0001c0001t0001g0056 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.178+2283_178+2303d others(23): Show |
GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 1354585 | ||||||
| chr16:1354585 | C | CAAAAAAA others(15): Show |
1 | a0001c0001t0001g0086 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.178+2282_178+2303d others(24): Show |
GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 1354585 | ||||||
| chr16:1354585 | CAAAA | C | 2 | a0001c0001t0001g0014 a0001c0001t0001g0095 |
7 | HG01109.hp2 HG02257.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.178+2300_178+2303d others(6): Show |
GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 1354585 | ||||||
| chr16:1354594 | A | AAAAAAAC others(8): Show |
1 | a0001c0001t0001g0082 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.178+2294_178+2295i others(17): Show |
GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 1354594 | ||||||
| chr16:1354602 | A | C | 1 | a0001c0001t0001g0082 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.178+2296A>C | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1354602 | |||||||
| chr16:1354610 | C | A | 2 | a0001c0001t0001g0002 a0001c0001t0001g0082 |
2 | HG00673.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.178+2304C>A | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1354610 | |||||||
| chr16:1354695 | T | A | 1 | a0001c0001t0001g0074 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.178+2389T>A | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1354695 | |||||||
| chr16:1354725 | T | C | 102 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(99): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.178+2419T>C | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1354725 | |||||||
| chr16:1354745 | C | T | 2 | a0001c0001t0001g0063 a0001c0001t0001g0065 |
2 | HG01074.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.178+2439C>T | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1354745 | |||||||
| chr16:1354897 | C | T | 1 | a0001c0001t0001g0070 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.178+2591C>T | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1354897 | |||||||
| chr16:1354929 | C | A | 1 | a0001c0001t0001g0075 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.178+2623C>A | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1354929 | |||||||
| chr16:1354950 | C | T | 2 | a0001c0001t0001g0084 a0001c0001t0001g0085 |
2 | HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.178+2644C>T | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1354950 | |||||||
| chr16:1355005 | G | C | 1 | a0001c0001t0001g0061 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.178+2699G>C | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1355005 | |||||||
| chr16:1355033 | GTGCGGGG others(25): Show |
G | 1 | a0001c0001t0001g0076 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.178+2752_178+2783d others(34): Show |
GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 1355033 | ||||||
| chr16:1355043 | G | A | 2 | a0001c0001t0001g0037 a0001c0001t0001g0081 |
3 | HG02965.hp2 NA18522.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.178+2737G>A | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1355043 | |||||||
| chr16:1355085 | GGTCTCCC others(89): Show |
G | 1 | a0001c0001t0001g0073 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.178+2794_178+2889d others(98): Show |
GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 1355085 | ||||||
| chr16:1355120 | C | T | 1 | a0001c0001t0001g0003 | 3 | HG02145.hp2 HG03098.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.178+2814C>T | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1355120 | |||||||
| chr16:1355127 | C | G | 1 | a0001c0001t0001g0082 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.178+2821C>G | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1355127 | |||||||
| chr16:1355164 | T | C | 1 | a0001c0001t0001g0082 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.178+2858T>C | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1355164 | |||||||
| chr16:1355171 | G | A | 1 | a0001c0001t0001g0032 | 2 | HG00741.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.178+2865G>A | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1355171 | |||||||
| chr16:1355181 | C | T | 1 | a0001c0001t0001g0002 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.178+2875C>T | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1355181 | |||||||
| chr16:1355191 | G | A | 4 | a0001c0001t0001g0023 a0001c0001t0001g0039 a0001c0001t0001g0100 others(1): Show |
7 | HG02451.hp1 HG02486.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.178+2885G>A | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1355191 | |||||||
| chr16:1355346 | C | T | 1 | a0001c0001t0001g0037 | 2 | HG02965.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.178+3040C>T | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1355346 | |||||||
| chr16:1355375 | C | G | 3 | a0001c0001t0001g0015 a0001c0001t0001g0069 a0001c0001t0001g0092 |
7 | HG00280.hp1 HG01081.hp2 NA18955.hp2 others(4): Show |
intron_variant | MODIFIER | c.178+3069C>G | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1355375 | |||||||
| chr16:1355384 | G | A | 3 | a0001c0001t0001g0017 a0001c0001t0001g0064 a0001c0001t0001g0096 |
6 | HG00639.hp1 HG02622.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.178+3078G>A | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1355384 | |||||||
| chr16:1355525 | G | C | 2 | a0001c0001t0001g0021 a0003c0005t0001g0103 |
4 | HG02258.hp1 HG02615.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.178+3219G>C | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1355525 | |||||||
| chr16:1355533 | C | T | 1 | a0001c0001t0001g0047 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.178+3227C>T | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1355533 | |||||||
| chr16:1355536 | C | T | 52 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(49): Show |
163 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(160): Show |
intron_variant | MODIFIER | c.178+3230C>T | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1355536 | |||||||
| chr16:1355663 | T | C | 89 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(86): Show |
344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.178+3357T>C | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1355663 | |||||||
| chr16:1355700 | G | C | 3 | a0001c0001t0001g0026 a0001c0001t0001g0084 a0001c0001t0001g0085 |
4 | HG02055.hp2 HG02723.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.178+3394G>C | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1355700 | |||||||
| chr16:1355969 | G | A | 5 | a0001c0001t0001g0016 a0001c0001t0001g0020 a0001c0001t0001g0050 others(2): Show |
11 | HG00099.hp1 HG00741.hp2 HG01106.hp2 others(8): Show |
intron_variant | MODIFIER | c.178+3663G>A | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1355969 | |||||||
| chr16:1356114 | G | A | 1 | a0001c0001t0001g0067 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.178+3808G>A | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1356114 | |||||||
| chr16:1356138 | A | G | 6 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0039 others(3): Show |
11 | HG02257.hp1 HG02451.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.178+3832A>G | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1356138 | |||||||
| chr16:1356141 | G | A | 2 | a0001c0001t0001g0019 a0004c0006t0002g0042 |
4 | HG02257.hp1 HG02922.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.178+3835G>A | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1356141 | |||||||
| chr16:1356242 | C | G | 1 | a0001c0001t0001g0071 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.178+3936C>G | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1356242 | |||||||
| chr16:1356251 | G | A | 4 | a0001c0001t0001g0023 a0001c0001t0001g0039 a0001c0001t0001g0100 others(1): Show |
7 | HG02451.hp1 HG02486.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.178+3945G>A | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1356251 | |||||||
| chr16:1356270 | G | A | 3 | a0001c0001t0001g0041 a0001c0001t0001g0058 a0001c0001t0001g0059 |
3 | HG01069.hp1 HG02970.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.178+3964G>A | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1356270 | |||||||
| chr16:1356483 | C | T | 1 | a0001c0001t0001g0032 | 2 | HG00741.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.178+4177C>T | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1356483 | |||||||
| chr16:1356496 | C | T | 2 | a0001c0001t0001g0060 a0001c0001t0001g0088 |
2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.178+4190C>T | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1356496 | |||||||
| chr16:1356508 | G | A | 2 | a0001c0001t0001g0068 a0006c0007t0001g0083 |
2 | NA18974.hp2 NA19059.hp2 |
intron_variant | MODIFIER | c.178+4202G>A | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1356508 | |||||||
| chr16:1356517 | G | A | 2 | a0001c0001t0001g0046 a0001c0001t0001g0086 |
2 | HG02738.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.178+4211G>A | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1356517 | |||||||
| chr16:1356563 | C | T | 3 | a0001c0001t0001g0039 a0001c0001t0001g0100 a0001c0001t0001g0101 |
4 | HG02451.hp1 HG02486.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.178+4257C>T | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1356563 | |||||||
| chr16:1356808 | CG | C | 3 | a0001c0001t0001g0017 a0001c0001t0001g0064 a0001c0001t0001g0096 |
6 | HG00639.hp1 HG02622.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.178+4503delG | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1356808 | |||||||
| chr16:1356857 | G | A | 3 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0097 |
3 | HG02559.hp2 HG02896.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.178+4551G>A | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1356857 | |||||||
| chr16:1356873 | CTGCGGGC others(35): Show |
C | 88 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(85): Show |
341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.178+4602_178+4643d others(44): Show |
GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 1356873 | ||||||
| chr16:1356881 | GGGGGTCT others(34): Show |
G | 1 | a0006c0007t0001g0083 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.178+4580_178+4620d others(43): Show |
GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 1356881 | ||||||
| chr16:1356901 | GTGCGGGC others(34): Show |
G | 1 | a0001c0001t0001g0038 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.178+4596_178+4636d others(43): Show |
GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1356901 | |||||||
| chr16:1356905 | GGGCGAGA others(34): Show |
G | 1 | a0001c0001t0001g0024 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.178+4602_178+4642d others(43): Show |
GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 1356905 | ||||||
| chr16:1356909 | G | T | 1 | a0001c0001t0001g0019 | 3 | HG02257.hp1 NA18906.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.178+4603G>T | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1356909 | |||||||
| chr16:1356925 | G | A | 1 | a0006c0007t0001g0083 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.178+4619G>A | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1356925 | |||||||
| chr16:1356925 | GGGTCTGC others(21): Show |
G | 1 | a0001c0001t0001g0019 | 3 | HG02257.hp1 NA18906.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.178+4631_178+4658d others(30): Show |
GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 1356925 | ||||||
| chr16:1356973 | G | C | 1 | a0001c0001t0001g0075 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.178+4667G>C | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1356973 | |||||||
| chr16:1357092 | G | T | 17 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(14): Show |
47 | HG00099.hp1 HG00423.hp2 HG00609.hp2 others(44): Show |
intron_variant | MODIFIER | c.179-4651G>T | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1357092 | |||||||
| chr16:1357130 | C | G | 1 | a0001c0001t0001g0036 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.179-4613C>G | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1357130 | |||||||
| chr16:1357180 | A | T | 1 | a0001c0001t0001g0038 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.179-4563A>T | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1357180 | |||||||
| chr16:1357241 | T | C | 5 | a0001c0001t0001g0008 a0001c0001t0001g0023 a0001c0001t0001g0039 others(2): Show |
8 | HG02451.hp1 HG02486.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.179-4502T>C | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1357241 | |||||||
| chr16:1357440 | A | G | 101 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(98): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.179-4303A>G | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1357440 | |||||||
| chr16:1357483 | T | TTTA | 14 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(11): Show |
37 | HG00140.hp1 HG00323.hp2 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.179-4235_179-4233d others(5): Show |
GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 1357483 | ||||||
| chr16:1357483 | T | TTTATTA | 4 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0023 others(1): Show |
8 | HG02258.hp1 HG02615.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.179-4238_179-4233d others(8): Show |
GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 1357483 | ||||||
| chr16:1357483 | TTTA | T | 4 | a0001c0001t0001g0017 a0001c0001t0001g0045 a0001c0001t0001g0064 others(1): Show |
7 | HG00639.hp1 HG01516.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.179-4235_179-4233d others(5): Show |
GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 1357483 | ||||||
| chr16:1357488 | T | C | 2 | a0001c0001t0001g0002 a0001c0001t0001g0006 |
2 | HG01106.hp1 HG01168.hp1 |
intron_variant | MODIFIER | c.179-4255T>C | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1357488 | |||||||
| chr16:1357522 | CGCTGTGT others(15): Show |
C | 3 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0097 |
3 | HG02559.hp2 HG02896.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.179-4196_179-4175d others(24): Show |
GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 1357522 | ||||||
| chr16:1357575 | G | A | 1 | a0001c0001t0001g0004 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.179-4168G>A | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1357575 | |||||||
| chr16:1357614 | C | T | 89 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(86): Show |
343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.179-4129C>T | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1357614 | |||||||
| chr16:1357739 | T | G | 4 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(1): Show |
4 | HG02559.hp2 HG02896.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.179-4004T>G | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1357739 | |||||||
| chr16:1357761 | C | T | 1 | a0001c0001t0001g0001 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.179-3982C>T | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1357761 | |||||||
| chr16:1357791 | T | C | 101 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(98): Show |
359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.179-3952T>C | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1357791 | |||||||
| chr16:1357791 | T | G | 1 | a0001c0001t0001g0013 | 7 | HG01069.hp2 HG01071.hp2 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.179-3952T>G | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1357791 | |||||||
| chr16:1357808 | T | C | 102 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(99): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.179-3935T>C | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1357808 | |||||||
| chr16:1358141 | C | T | 1 | a0001c0001t0001g0010 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.179-3602C>T | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1358141 | |||||||
| chr16:1358147 | G | T | 1 | a0006c0007t0001g0083 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.179-3596G>T | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1358147 | |||||||
| chr16:1358149 | G | T | 1 | a0001c0001t0001g0082 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.179-3594G>T | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1358149 | |||||||
| chr16:1358193 | TC | T | 8 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(5): Show |
17 | HG00140.hp2 HG00733.hp2 HG00738.hp2 others(14): Show |
intron_variant | MODIFIER | c.179-3545delC | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 1358193 | ||||||
| chr16:1358198 | C | G | 2 | a0001c0001t0001g0084 a0001c0001t0001g0085 |
2 | HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.179-3545C>G | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1358198 | |||||||
| chr16:1358250 | T | G | 1 | a0001c0001t0001g0007 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.179-3493T>G | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1358250 | |||||||
| chr16:1358277 | C | A | 1 | a0001c0001t0001g0013 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.179-3466C>A | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1358277 | |||||||
| chr16:1358336 | A | G | 4 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(1): Show |
4 | HG03491.hp2 HG03492.hp2 NA18973.hp1 others(1): Show |
intron_variant | MODIFIER | c.179-3407A>G | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1358336 | |||||||
| chr16:1358352 | T | C | 1 | a0001c0001t0001g0019 | 3 | HG02257.hp1 NA18906.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.179-3391T>C | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1358352 | |||||||
| chr16:1358359 | C | G | 1 | a0001c0001t0001g0013 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.179-3384C>G | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1358359 | |||||||
| chr16:1358506 | C | T | 1 | a0001c0001t0001g0003 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.179-3237C>T | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1358506 | |||||||
| chr16:1358741 | C | T | 1 | a0001c0001t0001g0018 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.179-3002C>T | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1358741 | |||||||
| chr16:1358755 | T | A | 1 | a0001c0001t0001g0038 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.179-2988T>A | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1358755 | |||||||
| chr16:1358823 | T | G | 1 | a0001c0001t0001g0063 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.179-2920T>G | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1358823 | |||||||
| chr16:1358857 | G | T | 2 | a0001c0001t0001g0068 a0006c0007t0001g0083 |
2 | NA18974.hp2 NA19059.hp2 |
intron_variant | MODIFIER | c.179-2886G>T | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1358857 | |||||||
| chr16:1358867 | CT | C | 98 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(95): Show |
360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.179-2864delT | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 1358867 | ||||||
| chr16:1358922 | C | T | 1 | a0001c0001t0001g0011 | 2 | HG02970.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.179-2821C>T | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1358922 | |||||||
| chr16:1358965 | G | C | 4 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0069 others(1): Show |
9 | HG00280.hp1 HG01081.hp2 NA18954.hp1 others(6): Show |
intron_variant | MODIFIER | c.179-2778G>C | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1358965 | |||||||
| chr16:1358999 | T | C | 1 | a0001c0001t0001g0019 | 3 | HG02257.hp1 NA18906.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.179-2744T>C | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1358999 | |||||||
| chr16:1359079 | A | G | 31 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(28): Show |
137 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(134): Show |
intron_variant | MODIFIER | c.179-2664A>G | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1359079 | |||||||
| chr16:1359210 | G | T | 2 | a0001c0001t0001g0068 a0006c0007t0001g0083 |
2 | NA18974.hp2 NA19059.hp2 |
intron_variant | MODIFIER | c.179-2533G>T | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1359210 | |||||||
| chr16:1359235 | C | G | 1 | a0001c0001t0001g0082 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.179-2508C>G | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1359235 | |||||||
| chr16:1359261 | C | T | 1 | a0001c0001t0001g0017 | 3 | HG00639.hp1 HG02622.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.179-2482C>T | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1359261 | |||||||
| chr16:1359331 | A | G | 1 | a0001c0001t0001g0002 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.179-2412A>G | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1359331 | |||||||
| chr16:1359548 | G | A | 1 | a0001c0001t0001g0014 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.179-2195G>A | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1359548 | |||||||
| chr16:1359583 | A | G | 1 | a0001c0001t0001g0012 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.179-2160A>G | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1359583 | |||||||
| chr16:1359589 | G | C | 1 | a0001c0001t0001g0004 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.179-2154G>C | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1359589 | |||||||
| chr16:1359657 | C | T | 1 | a0001c0001t0001g0082 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.179-2086C>T | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1359657 | |||||||
| chr16:1359691 | C | T | 2 | a0001c0001t0001g0001 a0001c0001t0001g0003 |
7 | HG00733.hp2 HG01934.hp1 HG01943.hp2 others(4): Show |
intron_variant | MODIFIER | c.179-2052C>T | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1359691 | |||||||
| chr16:1359743 | C | T | 4 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0060 others(1): Show |
4 | HG00099.hp2 HG01516.hp1 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.179-2000C>T | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1359743 | |||||||
| chr16:1359759 | G | A | 1 | a0001c0001t0001g0041 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.179-1984G>A | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1359759 | |||||||
| chr16:1359816 | T | C | 1 | a0001c0001t0001g0005 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.179-1927T>C | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1359816 | |||||||
| chr16:1359902 | G | A | 1 | a0001c0001t0001g0072 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.179-1841G>A | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1359902 | |||||||
| chr16:1359910 | G | A | 1 | a0001c0001t0001g0082 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.179-1833G>A | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1359910 | |||||||
| chr16:1360086 | G | A | 1 | a0001c0001t0001g0007 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.179-1657G>A | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1360086 | |||||||
| chr16:1360106 | C | CA | 8 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0012 others(5): Show |
11 | HG00735.hp2 HG02451.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.179-1625dupA | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 1360106 | ||||||
| chr16:1360106 | CA | C | 4 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0038 others(1): Show |
10 | HG00423.hp2 HG00609.hp2 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.179-1625delA | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 1360106 | ||||||
| chr16:1360132 | G | A | 48 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(45): Show |
192 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(189): Show |
intron_variant | MODIFIER | c.179-1611G>A | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1360132 | |||||||
| chr16:1360173 | G | A | 1 | a0001c0001t0001g0004 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.179-1570G>A | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1360173 | |||||||
| chr16:1360215 | T | A | 1 | a0001c0001t0001g0038 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.179-1528T>A | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1360215 | |||||||
| chr16:1360307 | C | CCTGTTTA others(3): Show |
1 | a0001c0001t0001g0002 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.179-1433_179-1424d others(12): Show |
GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 1360307 | ||||||
| chr16:1360556 | G | A | 1 | a0001c0001t0001g0026 | 2 | HG02055.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.179-1187G>A | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1360556 | |||||||
| chr16:1360593 | C | T | 1 | a0001c0001t0001g0028 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.179-1150C>T | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1360593 | |||||||
| chr16:1360641 | T | C | 1 | a0001c0001t0001g0096 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.179-1102T>C | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1360641 | |||||||
| chr16:1360723 | A | G | 3 | a0001c0001t0001g0026 a0001c0001t0001g0084 a0001c0001t0001g0085 |
4 | HG02055.hp2 HG02723.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.179-1020A>G | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1360723 | |||||||
| chr16:1360735 | C | T | 4 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(1): Show |
14 | HG00323.hp2 HG01255.hp1 HG01515.hp2 others(11): Show |
intron_variant | MODIFIER | c.179-1008C>T | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1360735 | |||||||
| chr16:1360837 | C | T | 3 | a0001c0001t0001g0017 a0001c0001t0001g0064 a0001c0001t0001g0096 |
6 | HG00639.hp1 HG02622.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.179-906C>T | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1360837 | |||||||
| chr16:1360875 | G | T | 1 | a0001c0001t0001g0017 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.179-868G>T | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1360875 | |||||||
| chr16:1360996 | G | T | 1 | a0001c0001t0001g0082 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.179-747G>T | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1360996 | |||||||
| chr16:1361061 | T | C | 1 | a0001c0001t0001g0002 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.179-682T>C | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1361061 | |||||||
| chr16:1361082 | G | A | 2 | a0001c0001t0001g0017 a0001c0001t0001g0064 |
5 | HG00639.hp1 HG02622.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.179-661G>A | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1361082 | |||||||
| chr16:1361106 | C | G | 1 | a0001c0001t0001g0001 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.179-637C>G | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1361106 | |||||||
| chr16:1361125 | A | T | 42 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(39): Show |
174 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(171): Show |
intron_variant | MODIFIER | c.179-618A>T | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1361125 | |||||||
| chr16:1361128 | C | T | 55 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(52): Show |
157 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.179-615C>T | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1361128 | |||||||
| chr16:1361367 | G | A | 2 | a0001c0001t0001g0002 a0001c0001t0001g0004 |
2 | HG00280.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.179-376G>A | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1361367 | |||||||
| chr16:1361382 | A | C | 1 | a0001c0001t0001g0013 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.179-361A>C | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1361382 | |||||||
| chr16:1361405 | G | A | 1 | a0006c0007t0001g0083 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.179-338G>A | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1361405 | |||||||
| chr16:1361406 | A | G | 1 | a0006c0007t0001g0083 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.179-337A>G | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1361406 | |||||||
| chr16:1361527 | C | T | 1 | a0001c0001t0001g0007 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.179-216C>T | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1361527 | |||||||
| chr16:1361560 | C | T | 1 | a0001c0001t0001g0008 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.179-183C>T | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1361560 | |||||||
| chr16:1361653 | G | A | 1 | a0006c0007t0001g0083 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.179-90G>A | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 3/10 | chr16 | 1361653 | |||||||
| chr16:1361804 | G | T | 3 | a0001c0001t0001g0017 a0001c0001t0001g0064 a0001c0001t0001g0096 |
6 | HG00639.hp1 HG02622.hp1 HG02647.hp1 others(3): Show |
splice_region_variant&intron_variant | LOW | c.233+7G>T | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 4/10 | chr16 | 1361804 | |||||||
| chr16:1362004 | C | T | 11 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(8): Show |
41 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.318-34C>T | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 5/10 | chr16 | 1362004 | |||||||
| chr16:1362014 | C | T | 1 | a0001c0001t0001g0019 | 3 | HG02257.hp1 NA18906.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.318-24C>T | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 5/10 | chr16 | 1362014 | |||||||
| chr16:1362020 | G | A | 1 | a0001c0001t0001g0037 | 2 | HG02965.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.318-18G>A | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 5/10 | chr16 | 1362020 | |||||||
| chr16:1362146 | GGGAGCCC others(7): Show |
G | 1 | a0001c0001t0001g0008 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.411+18_411+31delAG others(12): Show |
GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr16 | 1362146 | ||||||
| chr16:1362189 | C | T | 2 | a0001c0001t0001g0007 a0001c0001t0001g0022 |
4 | HG02258.hp2 HG03041.hp1 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.412-17C>T | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 6/10 | chr16 | 1362189 | |||||||
| chr16:1362192 | C | T | 1 | a0001c0001t0001g0002 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.412-14C>T | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 6/10 | chr16 | 1362192 | |||||||
| chr16:1362361 | G | A | 2 | a0001c0001t0001g0037 a0005c0004t0001g0091 |
3 | HG02922.hp2 HG02965.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.526+41G>A | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 7/10 | chr16 | 1362361 | |||||||
| chr16:1362751 | T | C | 1 | a0001c0002t0001g0005 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.741+9T>C | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 9/10 | chr16 | 1362751 | |||||||
| chr16:1362964 | C | T | 1 | a0001c0001t0001g0019 | 3 | HG02257.hp1 NA18906.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.824-33C>T | GNPTG | ENSG00000090581.11 | transcript | ENST00000204679.9 | protein_coding | 10/10 | chr16 | 1362964 |