Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 348487 |
| ensemblid | ENSG00000185519.9 |
| hgncid | 26717 |
| symbol | FAM131C |
| name | family with sequence similarity 131 member C |
| refseq_nuc | NM_182623.3 |
| refseq_prot | NP_872429.2 |
| ensembl_nuc | ENST00000375662.5 |
| ensembl_prot | ENSP00000364814.4 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 16057769 |
| end | 16073651 |
| strand | - |
| ver | v1.2 |
| region | chr1:16057769-16073651 |
| region5000 | chr1:16052769-16078651 |
| regionname0 | FAM131C_chr1_16057769_16073651 |
| regionname5000 | FAM131C_chr1_16052769_16078651 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 280 | 162 | 7 | 24 | 115 | 1 | 15 | 86 | FAM131C_chr1_16052769_16078651 | FAM131C | MGSCV others(275): Show |
chr1 | 16052769 | 16078651 |
| a0002 | 0/1 | 280 | 68 | 24 | 22 | 1 | 9 | 11 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | MGSCV others(275): Show |
chr1 | 16052769 | 16078651 |
| a0003 | 0/0 | 280 | 58 | 33 | 16 | 0 | 4 | 5 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | MGSCV others(275): Show |
chr1 | 16052769 | 16078651 |
| a0004 | 1/0 | 280 | 41 | 1 | 5 | 29 | 1 | 4 | 19 | FAM131C_chr1_16052769_16078651 | FAM131C | MGSCV others(275): Show |
chr1 | 16052769 | 16078651 |
| a0005 | 0/0 | 280 | 14 | 11 | 2 | 0 | 0 | 1 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | MGSCV others(275): Show |
chr1 | 16052769 | 16078651 |
| a0006 | 0/0 | 280 | 11 | 10 | 1 | 0 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | MGSCV others(275): Show |
chr1 | 16052769 | 16078651 |
| a0007 | 0/0 | 280 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | MGSCV others(275): Show |
chr1 | 16052769 | 16078651 |
| a0008 | 0/0 | 280 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | MGSCV others(275): Show |
chr1 | 16052769 | 16078651 |
| a0009 | 0/0 | 280 | 3 | 1 | 0 | 0 | 1 | 1 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | MGSCV others(275): Show |
chr1 | 16052769 | 16078651 |
| a0010 | 0/0 | 280 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | MGSCV others(275): Show |
chr1 | 16052769 | 16078651 |
| a0011 | 0/0 | 280 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | MGSCV others(275): Show |
chr1 | 16052769 | 16078651 |
| a0012 | 0/0 | 280 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | MGSCV others(275): Show |
chr1 | 16052769 | 16078651 |
| a0013 | 0/0 | 280 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | MGSCV others(275): Show |
chr1 | 16052769 | 16078651 |
| a0014 | 0/0 | 280 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | MGSCV others(275): Show |
chr1 | 16052769 | 16078651 |
| a0015 | 0/0 | 280 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | MGSCV others(275): Show |
chr1 | 16052769 | 16078651 |
| a0016 | 0/0 | 280 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | MGSCV others(275): Show |
chr1 | 16052769 | 16078651 |
| a0017 | 0/0 | 280 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | MGSCV others(275): Show |
chr1 | 16052769 | 16078651 |
| a0018 | 0/0 | 280 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FAM131C_chr1_16052769_16078651 | FAM131C | MGSCV others(275): Show |
chr1 | 16052769 | 16078651 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 840 | 161 | 7 | 24 | 114 | 1 | 15 | FAM131C_chr1_16052769_16078651 | FAM131C | ATGGG others(835): Show |
chr1 | 16052769 | 16078651 | ||
| a0001c0016 | 0/0 | 840 | 1 | 0 | 0 | 1 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | ATGGG others(835): Show |
chr1 | 16052769 | 16078651 | ||
| a0002c0002 | 0/1 | 840 | 67 | 24 | 22 | 1 | 9 | 10 | FAM131C_chr1_16052769_16078651 | FAM131C | ATGGG others(835): Show |
chr1 | 16052769 | 16078651 | ||
| a0002c0024 | 0/0 | 840 | 1 | 0 | 0 | 0 | 0 | 1 | FAM131C_chr1_16052769_16078651 | FAM131C | ATGGG others(835): Show |
chr1 | 16052769 | 16078651 | ||
| a0003c0003 | 0/0 | 840 | 56 | 31 | 16 | 0 | 4 | 5 | FAM131C_chr1_16052769_16078651 | FAM131C | ATGGG others(835): Show |
chr1 | 16052769 | 16078651 | ||
| a0003c0013 | 0/0 | 840 | 1 | 1 | 0 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | ATGGG others(835): Show |
chr1 | 16052769 | 16078651 | ||
| a0003c0018 | 0/0 | 840 | 1 | 1 | 0 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | ATGGG others(835): Show |
chr1 | 16052769 | 16078651 | ||
| a0004c0004 | 1/0 | 840 | 35 | 1 | 4 | 26 | 0 | 3 | FAM131C_chr1_16052769_16078651 | FAM131C | ATGGG others(835): Show |
chr1 | 16052769 | 16078651 | ||
| a0004c0007 | 0/0 | 840 | 5 | 0 | 0 | 3 | 1 | 1 | FAM131C_chr1_16052769_16078651 | FAM131C | ATGGG others(835): Show |
chr1 | 16052769 | 16078651 | ||
| a0004c0012 | 0/0 | 840 | 1 | 0 | 1 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | ATGGG others(835): Show |
chr1 | 16052769 | 16078651 | ||
| a0005c0005 | 0/0 | 840 | 14 | 11 | 2 | 0 | 0 | 1 | FAM131C_chr1_16052769_16078651 | FAM131C | ATGGG others(835): Show |
chr1 | 16052769 | 16078651 | ||
| a0006c0006 | 0/0 | 840 | 11 | 10 | 1 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | ATGGG others(835): Show |
chr1 | 16052769 | 16078651 | ||
| a0007c0008 | 0/0 | 840 | 4 | 4 | 0 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | ATGGG others(835): Show |
chr1 | 16052769 | 16078651 | ||
| a0007c0014 | 0/0 | 840 | 1 | 1 | 0 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | ATGGG others(835): Show |
chr1 | 16052769 | 16078651 | ||
| a0008c0010 | 0/0 | 840 | 3 | 2 | 1 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | ATGGG others(835): Show |
chr1 | 16052769 | 16078651 | ||
| a0009c0009 | 0/0 | 840 | 3 | 1 | 0 | 0 | 1 | 1 | FAM131C_chr1_16052769_16078651 | FAM131C | ATGGG others(835): Show |
chr1 | 16052769 | 16078651 | ||
| a0010c0011 | 0/0 | 840 | 3 | 3 | 0 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | ATGGG others(835): Show |
chr1 | 16052769 | 16078651 | ||
| a0011c0021 | 0/0 | 840 | 1 | 0 | 1 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | ATGGG others(835): Show |
chr1 | 16052769 | 16078651 | ||
| a0012c0022 | 0/0 | 840 | 1 | 0 | 1 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | ATGGG others(835): Show |
chr1 | 16052769 | 16078651 | ||
| a0013c0020 | 0/0 | 840 | 1 | 0 | 1 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | ATGGG others(835): Show |
chr1 | 16052769 | 16078651 | ||
| a0014c0017 | 0/0 | 840 | 1 | 0 | 1 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | ATGGG others(835): Show |
chr1 | 16052769 | 16078651 | ||
| a0015c0023 | 0/0 | 840 | 1 | 0 | 1 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | ATGGG others(835): Show |
chr1 | 16052769 | 16078651 | ||
| a0016c0019 | 0/0 | 840 | 1 | 0 | 0 | 0 | 0 | 1 | FAM131C_chr1_16052769_16078651 | FAM131C | ATGGG others(835): Show |
chr1 | 16052769 | 16078651 | ||
| a0017c0025 | 0/0 | 840 | 1 | 1 | 0 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | ATGGG others(835): Show |
chr1 | 16052769 | 16078651 | ||
| a0018c0015 | 0/0 | 840 | 1 | 0 | 0 | 1 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | ATGGG others(835): Show |
chr1 | 16052769 | 16078651 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 1720 | 125 | 4 | 20 | 88 | 0 | 13 | FAM131C_chr1_16052769_16078651 | FAM131C | ACTGC others(1715): Show |
chr1 | 16052769 | 16078651 |
| a0001c0001t0006 | 0/0 | 1720 | 19 | 0 | 0 | 19 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | ACTGC others(1715): Show |
chr1 | 16052769 | 16078651 |
| a0001c0001t0009 | 0/0 | 1720 | 7 | 3 | 3 | 0 | 1 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | ACTGC others(1715): Show |
chr1 | 16052769 | 16078651 |
| a0001c0001t0011 | 0/0 | 1720 | 1 | 0 | 0 | 0 | 0 | 1 | FAM131C_chr1_16052769_16078651 | FAM131C | ACTGC others(1715): Show |
chr1 | 16052769 | 16078651 |
| a0001c0001t0017 | 0/0 | 1720 | 2 | 0 | 0 | 2 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | ACTGC others(1715): Show |
chr1 | 16052769 | 16078651 |
| a0001c0001t0020 | 0/0 | 1720 | 1 | 0 | 1 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | ACTGC others(1715): Show |
chr1 | 16052769 | 16078651 |
| a0001c0001t0021 | 0/0 | 1720 | 1 | 0 | 0 | 1 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | ACTGC others(1715): Show |
chr1 | 16052769 | 16078651 |
| a0001c0001t0022 | 0/0 | 1720 | 1 | 0 | 0 | 1 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | ACTGC others(1715): Show |
chr1 | 16052769 | 16078651 |
| a0001c0001t0023 | 0/0 | 1720 | 1 | 0 | 0 | 0 | 0 | 1 | FAM131C_chr1_16052769_16078651 | FAM131C | ACTGC others(1715): Show |
chr1 | 16052769 | 16078651 |
| a0001c0001t0024 | 0/0 | 1720 | 1 | 0 | 0 | 1 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | ACTGC others(1715): Show |
chr1 | 16052769 | 16078651 |
| a0001c0001t0026 | 0/0 | 1720 | 1 | 0 | 0 | 1 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | ACTGC others(1715): Show |
chr1 | 16052769 | 16078651 |
| a0001c0001t0036 | 0/0 | 1720 | 1 | 0 | 0 | 1 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | ACTGC others(1715): Show |
chr1 | 16052769 | 16078651 |
| a0001c0016t0029 | 0/0 | 1720 | 1 | 0 | 0 | 1 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | ACTGC others(1715): Show |
chr1 | 16052769 | 16078651 |
| a0002c0002t0002 | 0/1 | 1720 | 58 | 19 | 22 | 1 | 9 | 6 | FAM131C_chr1_16052769_16078651 | FAM131C | ACTGC others(1715): Show |
chr1 | 16052769 | 16078651 |
| a0002c0002t0011 | 0/0 | 1720 | 2 | 2 | 0 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | ACTGC others(1715): Show |
chr1 | 16052769 | 16078651 |
| a0002c0002t0014 | 0/0 | 1720 | 4 | 0 | 0 | 0 | 0 | 4 | FAM131C_chr1_16052769_16078651 | FAM131C | ACTGC others(1715): Show |
chr1 | 16052769 | 16078651 |
| a0002c0002t0019 | 0/0 | 1750 | 1 | 1 | 0 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | ACTGC others(1745): Show |
chr1 | 16052769 | 16078651 |
| a0002c0002t0030 | 0/0 | 1720 | 1 | 1 | 0 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | ACTGC others(1715): Show |
chr1 | 16052769 | 16078651 |
| a0002c0002t0033 | 0/0 | 1720 | 1 | 1 | 0 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | ACTGC others(1715): Show |
chr1 | 16052769 | 16078651 |
| a0002c0024t0002 | 0/0 | 1720 | 1 | 0 | 0 | 0 | 0 | 1 | FAM131C_chr1_16052769_16078651 | FAM131C | ACTGC others(1715): Show |
chr1 | 16052769 | 16078651 |
| a0003c0003t0003 | 0/0 | 1720 | 39 | 20 | 12 | 0 | 3 | 4 | FAM131C_chr1_16052769_16078651 | FAM131C | ACTGC others(1715): Show |
chr1 | 16052769 | 16078651 |
| a0003c0003t0007 | 0/0 | 1720 | 11 | 10 | 1 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | ACTGC others(1715): Show |
chr1 | 16052769 | 16078651 |
| a0003c0003t0008 | 0/0 | 1720 | 5 | 0 | 3 | 0 | 1 | 1 | FAM131C_chr1_16052769_16078651 | FAM131C | ACTGC others(1715): Show |
chr1 | 16052769 | 16078651 |
| a0003c0003t0012 | 0/0 | 1720 | 1 | 1 | 0 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | ACTGC others(1715): Show |
chr1 | 16052769 | 16078651 |
| a0003c0013t0035 | 0/0 | 1720 | 1 | 1 | 0 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | ACTGC others(1715): Show |
chr1 | 16052769 | 16078651 |
| a0003c0018t0007 | 0/0 | 1720 | 1 | 1 | 0 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | ACTGC others(1715): Show |
chr1 | 16052769 | 16078651 |
| a0004c0004t0004 | 1/0 | 1720 | 16 | 0 | 0 | 15 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | ACTGC others(1715): Show |
chr1 | 16052769 | 16078651 |
| a0004c0004t0005 | 0/0 | 1720 | 19 | 1 | 4 | 11 | 0 | 3 | FAM131C_chr1_16052769_16078651 | FAM131C | ACTGC others(1715): Show |
chr1 | 16052769 | 16078651 |
| a0004c0007t0004 | 0/0 | 1720 | 5 | 0 | 0 | 3 | 1 | 1 | FAM131C_chr1_16052769_16078651 | FAM131C | ACTGC others(1715): Show |
chr1 | 16052769 | 16078651 |
| a0004c0012t0004 | 0/0 | 1720 | 1 | 0 | 1 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | ACTGC others(1715): Show |
chr1 | 16052769 | 16078651 |
| a0005c0005t0001 | 0/0 | 1720 | 1 | 0 | 0 | 0 | 0 | 1 | FAM131C_chr1_16052769_16078651 | FAM131C | ACTGC others(1715): Show |
chr1 | 16052769 | 16078651 |
| a0005c0005t0002 | 0/0 | 1720 | 1 | 0 | 1 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | ACTGC others(1715): Show |
chr1 | 16052769 | 16078651 |
| a0005c0005t0010 | 0/0 | 1720 | 6 | 6 | 0 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | ACTGC others(1715): Show |
chr1 | 16052769 | 16078651 |
| a0005c0005t0011 | 0/0 | 1720 | 3 | 3 | 0 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | ACTGC others(1715): Show |
chr1 | 16052769 | 16078651 |
| a0005c0005t0018 | 0/0 | 1720 | 2 | 1 | 1 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | ACTGC others(1715): Show |
chr1 | 16052769 | 16078651 |
| a0005c0005t0031 | 0/0 | 1720 | 1 | 1 | 0 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | ACTGC others(1715): Show |
chr1 | 16052769 | 16078651 |
| a0006c0006t0008 | 0/0 | 1720 | 1 | 1 | 0 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | ACTGC others(1715): Show |
chr1 | 16052769 | 16078651 |
| a0006c0006t0012 | 0/0 | 1720 | 4 | 3 | 1 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | ACTGC others(1715): Show |
chr1 | 16052769 | 16078651 |
| a0006c0006t0015 | 0/0 | 1720 | 2 | 2 | 0 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | ACTGC others(1715): Show |
chr1 | 16052769 | 16078651 |
| a0006c0006t0016 | 0/0 | 1720 | 2 | 2 | 0 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | ACTGC others(1715): Show |
chr1 | 16052769 | 16078651 |
| a0006c0006t0027 | 0/0 | 1720 | 1 | 1 | 0 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | ACTGC others(1715): Show |
chr1 | 16052769 | 16078651 |
| a0006c0006t0032 | 0/0 | 1720 | 1 | 1 | 0 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | ACTGC others(1715): Show |
chr1 | 16052769 | 16078651 |
| a0007c0008t0013 | 0/0 | 1720 | 4 | 4 | 0 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | ACTGC others(1715): Show |
chr1 | 16052769 | 16078651 |
| a0007c0014t0028 | 0/0 | 1720 | 1 | 1 | 0 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | ACTGC others(1715): Show |
chr1 | 16052769 | 16078651 |
| a0008c0010t0008 | 0/0 | 1720 | 3 | 2 | 1 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | ACTGC others(1715): Show |
chr1 | 16052769 | 16078651 |
| a0009c0009t0003 | 0/0 | 1720 | 3 | 1 | 0 | 0 | 1 | 1 | FAM131C_chr1_16052769_16078651 | FAM131C | ACTGC others(1715): Show |
chr1 | 16052769 | 16078651 |
| a0010c0011t0004 | 0/0 | 1720 | 2 | 2 | 0 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | ACTGC others(1715): Show |
chr1 | 16052769 | 16078651 |
| a0010c0011t0034 | 0/0 | 1720 | 1 | 1 | 0 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | ACTGC others(1715): Show |
chr1 | 16052769 | 16078651 |
| a0011c0021t0001 | 0/0 | 1720 | 1 | 0 | 1 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | ACTGC others(1715): Show |
chr1 | 16052769 | 16078651 |
| a0012c0022t0025 | 0/0 | 1720 | 1 | 0 | 1 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | ACTGC others(1715): Show |
chr1 | 16052769 | 16078651 |
| a0013c0020t0003 | 0/0 | 1720 | 1 | 0 | 1 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | ACTGC others(1715): Show |
chr1 | 16052769 | 16078651 |
| a0014c0017t0003 | 0/0 | 1720 | 1 | 0 | 1 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | ACTGC others(1715): Show |
chr1 | 16052769 | 16078651 |
| a0015c0023t0002 | 0/0 | 1720 | 1 | 0 | 1 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | ACTGC others(1715): Show |
chr1 | 16052769 | 16078651 |
| a0016c0019t0003 | 0/0 | 1720 | 1 | 0 | 0 | 0 | 0 | 1 | FAM131C_chr1_16052769_16078651 | FAM131C | ACTGC others(1715): Show |
chr1 | 16052769 | 16078651 |
| a0017c0025t0004 | 0/0 | 1720 | 1 | 1 | 0 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | ACTGC others(1715): Show |
chr1 | 16052769 | 16078651 |
| a0018c0015t0001 | 0/0 | 1720 | 1 | 0 | 0 | 1 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | ACTGC others(1715): Show |
chr1 | 16052769 | 16078651 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 40 | 0 | 9 | 24 | 0 | 7 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0001c0001t0001g0003 | 0/0 | 13 | 0 | 2 | 11 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0001c0001t0001g0007 | 0/0 | 8 | 0 | 4 | 3 | 0 | 1 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0001c0001t0001g0008 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0001c0001t0001g0009 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0001c0001t0001g0011 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0001c0001t0001g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0001c0001t0001g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0001c0001t0001g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0001c0001t0006g0014 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0001c0001t0006g0019 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0001c0001t0006g0054 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0001c0001t0006g0055 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0001c0001t0006g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0001c0001t0006g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0001c0001t0006g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0001c0001t0006g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0001c0001t0006g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0001c0001t0009g0017 | 0/0 | 4 | 2 | 1 | 0 | 1 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0001c0001t0009g0031 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0001c0001t0009g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0001c0001t0011g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0001c0001t0017g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0001c0001t0020g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0001c0001t0021g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0001c0001t0022g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0001c0001t0023g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0001c0001t0024g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0001c0001t0026g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0001c0001t0036g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0001c0016t0029g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0002c0002t0002g0002 | 0/0 | 18 | 0 | 11 | 1 | 4 | 2 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0002c0002t0002g0006 | 0/0 | 9 | 6 | 3 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0002c0002t0002g0013 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0002c0002t0002g0018 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0002c0002t0002g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0002c0002t0002g0043 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0002c0002t0002g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0002c0002t0002g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0002c0002t0002g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0002c0002t0002g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0002c0002t0002g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0002c0002t0002g0127 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0002c0002t0002g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0002c0002t0002g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0002c0002t0002g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0002c0002t0002g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0002c0002t0002g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0002c0002t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0002c0002t0002g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0002c0002t0002g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0002c0002t0002g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0002c0002t0002g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0002c0002t0002g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0002c0002t0011g0053 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0002c0002t0014g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0002c0002t0014g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0002c0002t0014g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0002c0002t0014g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0002c0002t0019g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0002c0002t0030g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0002c0002t0033g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0002c0024t0002g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0003c0003t0003g0005 | 0/0 | 9 | 2 | 6 | 0 | 0 | 1 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0003c0003t0003g0012 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0003c0003t0003g0015 | 0/0 | 5 | 2 | 3 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0003c0003t0003g0038 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0003c0003t0003g0039 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0003c0003t0003g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0003c0003t0003g0042 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0003c0003t0003g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0003c0003t0003g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0003c0003t0003g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0003c0003t0003g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0003c0003t0003g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0003c0003t0003g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0003c0003t0003g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0003c0003t0003g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0003c0003t0003g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0003c0003t0003g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0003c0003t0003g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0003c0003t0007g0024 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0003c0003t0007g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0003c0003t0007g0050 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0003c0003t0007g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0003c0003t0007g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0003c0003t0007g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0003c0003t0007g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0003c0003t0008g0051 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0003c0003t0008g0052 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0003c0003t0008g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0003c0003t0012g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0003c0013t0035g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0003c0018t0007g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0004c0004t0004g0010 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0004c0004t0004g0022 | 1/0 | 3 | 0 | 0 | 2 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0004c0004t0004g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0004c0004t0004g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0004c0004t0004g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0004c0004t0004g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0004c0004t0004g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0004c0004t0004g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0004c0004t0005g0004 | 0/0 | 10 | 0 | 1 | 9 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0004c0004t0005g0023 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0004c0004t0005g0048 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0004c0004t0005g0049 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0004c0004t0005g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0004c0004t0005g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0004c0007t0004g0041 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0004c0007t0004g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0004c0007t0004g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0004c0007t0004g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0004c0012t0004g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0005c0005t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0005c0005t0002g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0005c0005t0010g0016 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0005c0005t0010g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0005c0005t0010g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0005c0005t0011g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0005c0005t0011g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0005c0005t0011g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0005c0005t0018g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0005c0005t0018g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0005c0005t0031g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0006c0006t0008g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0006c0006t0012g0044 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0006c0006t0012g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0006c0006t0012g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0006c0006t0015g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0006c0006t0016g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0006c0006t0027g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0006c0006t0032g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0007c0008t0013g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0007c0008t0013g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0007c0008t0013g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0007c0014t0028g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0008c0010t0008g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0008c0010t0008g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0008c0010t0008g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0009c0009t0003g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0009c0009t0003g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0009c0009t0003g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0010c0011t0004g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0010c0011t0034g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0011c0021t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0012c0022t0025g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0013c0020t0003g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0014c0017t0003g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0015c0023t0002g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0016c0019t0003g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0017c0025t0004g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| a0018c0015t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0002 | t0002 | g0002 | EUR | GBR | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG00099 | hp2 | a0002 | c0002 | t0002 | g0129 | EUR | GBR | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG00140 | hp1 | a0001 | c0001 | t0009 | g0017 | EUR | GBR | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG00140 | hp2 | a0002 | c0002 | t0002 | g0018 | EUR | GBR | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG00280 | hp1 | a0004 | c0007 | t0004 | g0041 | EUR | FIN | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG00280 | hp2 | a0002 | c0002 | t0002 | g0132 | EUR | FIN | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG00323 | hp1 | a0002 | c0002 | t0002 | g0043 | EUR | FIN | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG00323 | hp2 | a0003 | c0003 | t0008 | g0052 | EUR | FIN | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG00408 | hp1 | a0001 | c0001 | t0006 | g0014 | EAS | CHS | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | CHS | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG00438 | hp2 | a0004 | c0004 | t0005 | g0004 | EAS | CHS | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG00544 | hp2 | a0004 | c0004 | t0004 | g0010 | EAS | CHS | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | CHS | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG00597 | hp1 | a0001 | c0001 | t0006 | g0177 | EAS | CHS | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG00621 | hp1 | a0004 | c0004 | t0004 | g0035 | EAS | CHS | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG00639 | hp1 | a0003 | c0003 | t0003 | g0015 | AMR | PUR | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG00639 | hp2 | a0002 | c0002 | t0002 | g0002 | AMR | PUR | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG00642 | hp1 | a0008 | c0010 | t0008 | g0168 | AMR | PUR | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG00642 | hp2 | a0011 | c0021 | t0001 | g0088 | AMR | PUR | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG00673 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | CHS | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG00673 | hp2 | a0004 | c0007 | t0004 | g0119 | EAS | CHS | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG00735 | hp2 | a0012 | c0022 | t0025 | g0139 | AMR | PUR | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG00738 | hp1 | a0001 | c0001 | t0020 | g0085 | AMR | PUR | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG00738 | hp2 | a0003 | c0003 | t0003 | g0005 | AMR | PUR | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG00741 | hp1 | a0002 | c0002 | t0002 | g0002 | AMR | PUR | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG01069 | hp1 | a0002 | c0002 | t0002 | g0043 | AMR | PUR | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG01069 | hp2 | a0003 | c0003 | t0003 | g0038 | AMR | PUR | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG01070 | hp1 | a0002 | c0002 | t0002 | g0006 | AMR | PUR | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG01071 | hp1 | a0003 | c0003 | t0003 | g0038 | AMR | PUR | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG01071 | hp2 | a0002 | c0002 | t0002 | g0006 | AMR | PUR | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG01074 | hp2 | a0003 | c0003 | t0003 | g0092 | AMR | PUR | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG01081 | hp1 | a0002 | c0002 | t0002 | g0018 | AMR | PUR | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG01099 | hp1 | a0003 | c0003 | t0003 | g0015 | AMR | PUR | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG01099 | hp2 | a0002 | c0002 | t0002 | g0117 | AMR | PUR | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG01106 | hp1 | a0013 | c0020 | t0003 | g0116 | AMR | PUR | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG01106 | hp2 | a0003 | c0003 | t0007 | g0050 | AMR | PUR | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG01109 | hp1 | a0002 | c0002 | t0002 | g0002 | AMR | PUR | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG01109 | hp2 | a0002 | c0002 | t0002 | g0006 | AMR | PUR | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG01167 | hp1 | a0003 | c0003 | t0008 | g0051 | AMR | PUR | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG01167 | hp2 | a0006 | c0006 | t0012 | g0044 | AMR | PUR | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG01168 | hp1 | a0002 | c0002 | t0002 | g0018 | AMR | PUR | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG01168 | hp2 | a0001 | c0001 | t0009 | g0031 | AMR | PUR | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG01169 | hp1 | a0002 | c0002 | t0002 | g0018 | AMR | PUR | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG01169 | hp2 | a0003 | c0003 | t0008 | g0051 | AMR | PUR | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | PUR | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG01175 | hp2 | a0002 | c0002 | t0002 | g0140 | AMR | PUR | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG01192 | hp1 | a0003 | c0003 | t0003 | g0005 | AMR | PUR | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG01243 | hp1 | a0002 | c0002 | t0002 | g0002 | AMR | PUR | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG01243 | hp2 | a0005 | c0005 | t0018 | g0159 | AMR | PUR | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG01255 | hp1 | a0001 | c0001 | t0009 | g0082 | AMR | CLM | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG01256 | hp1 | a0004 | c0004 | t0005 | g0004 | AMR | CLM | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG01256 | hp2 | a0003 | c0003 | t0003 | g0005 | AMR | CLM | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG01257 | hp2 | a0003 | c0003 | t0003 | g0015 | AMR | CLM | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG01258 | hp1 | a0003 | c0003 | t0003 | g0005 | AMR | CLM | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG01261 | hp1 | a0003 | c0003 | t0003 | g0005 | AMR | CLM | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG01346 | hp2 | a0001 | c0001 | t0009 | g0017 | AMR | CLM | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | CLM | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG01361 | hp1 | a0002 | c0002 | t0002 | g0002 | AMR | CLM | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG01361 | hp2 | a0014 | c0017 | t0003 | g0075 | AMR | CLM | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG01433 | hp1 | a0002 | c0002 | t0002 | g0002 | AMR | CLM | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG01433 | hp2 | a0004 | c0004 | t0005 | g0152 | AMR | CLM | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | CLM | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG01496 | hp2 | a0003 | c0003 | t0003 | g0005 | AMR | CLM | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG01515 | hp1 | a0002 | c0002 | t0002 | g0002 | EUR | IBS | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG01515 | hp2 | a0009 | c0009 | t0003 | g0106 | EUR | IBS | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG01516 | hp1 | a0003 | c0003 | t0003 | g0042 | EUR | IBS | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG01516 | hp2 | a0002 | c0002 | t0002 | g0002 | EUR | IBS | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG01517 | hp1 | a0003 | c0003 | t0003 | g0042 | EUR | IBS | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG01517 | hp2 | a0002 | c0002 | t0002 | g0002 | EUR | IBS | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG01884 | hp1 | a0002 | c0002 | t0002 | g0027 | AFR | ACB | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG01884 | hp2 | a0007 | c0008 | t0013 | g0112 | AFR | ACB | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG01891 | hp1 | a0003 | c0003 | t0003 | g0012 | AFR | ACB | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG01891 | hp2 | a0003 | c0018 | t0007 | g0155 | AFR | ACB | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG01928 | hp1 | a0002 | c0002 | t0002 | g0131 | AMR | PEL | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG01928 | hp2 | a0005 | c0005 | t0002 | g0068 | AMR | PEL | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG01934 | hp1 | a0004 | c0004 | t0005 | g0151 | AMR | PEL | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG01934 | hp2 | a0003 | c0003 | t0008 | g0052 | AMR | PEL | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG01943 | hp2 | a0002 | c0002 | t0002 | g0124 | AMR | PEL | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG01952 | hp1 | a0004 | c0004 | t0005 | g0023 | AMR | PEL | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG01952 | hp2 | a0002 | c0002 | t0002 | g0002 | AMR | PEL | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG01978 | hp1 | a0002 | c0002 | t0002 | g0002 | AMR | PEL | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG01978 | hp2 | a0015 | c0023 | t0002 | g0128 | AMR | PEL | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | PEL | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG01993 | hp1 | a0002 | c0002 | t0002 | g0002 | AMR | PEL | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PEL | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG02015 | hp2 | a0001 | c0001 | t0017 | g0030 | EAS | KHV | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG02040 | hp2 | a0001 | c0001 | t0017 | g0030 | EAS | KHV | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | KHV | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG02074 | hp2 | a0001 | c0001 | t0006 | g0019 | EAS | KHV | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG02080 | hp1 | a0001 | c0001 | t0006 | g0014 | EAS | KHV | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG02080 | hp2 | a0001 | c0001 | t0006 | g0019 | EAS | KHV | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG02083 | hp2 | a0004 | c0004 | t0004 | g0010 | EAS | KHV | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | KHV | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG02129 | hp2 | a0004 | c0004 | t0004 | g0010 | EAS | KHV | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG02132 | hp1 | a0004 | c0004 | t0004 | g0010 | EAS | KHV | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | KHV | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG02145 | hp1 | a0003 | c0003 | t0012 | g0111 | AFR | ACB | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG02145 | hp2 | a0003 | c0003 | t0003 | g0005 | AFR | ACB | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG02155 | hp1 | a0004 | c0004 | t0004 | g0035 | EAS | CDX | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG02165 | hp2 | a0004 | c0004 | t0004 | g0090 | EAS | CDX | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG02257 | hp1 | a0007 | c0008 | t0013 | g0037 | AFR | ACB | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG02257 | hp2 | a0003 | c0003 | t0003 | g0115 | AFR | ACB | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG02258 | hp1 | a0003 | c0003 | t0003 | g0103 | AFR | ACB | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG02258 | hp2 | a0002 | c0002 | t0019 | g0136 | AFR | ACB | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG02273 | hp1 | a0002 | c0002 | t0002 | g0002 | AMR | PEL | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG02280 | hp1 | a0005 | c0005 | t0010 | g0016 | AFR | ACB | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG02280 | hp2 | a0001 | c0001 | t0009 | g0017 | AFR | ACB | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG02451 | hp1 | a0005 | c0005 | t0010 | g0016 | AFR | ACB | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG02451 | hp2 | a0001 | c0001 | t0009 | g0031 | AFR | ACB | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | KHV | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | KHV | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG02572 | hp1 | a0006 | c0006 | t0012 | g0058 | AFR | GWD | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG02572 | hp2 | a0003 | c0013 | t0035 | g0171 | AFR | GWD | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0074 | SAS | PJL | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG02602 | hp2 | a0002 | c0002 | t0002 | g0096 | SAS | PJL | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG02615 | hp1 | a0006 | c0006 | t0008 | g0160 | AFR | GWD | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG02615 | hp2 | a0003 | c0003 | t0007 | g0156 | AFR | GWD | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG02622 | hp1 | a0007 | c0014 | t0028 | g0154 | AFR | GWD | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG02622 | hp2 | a0003 | c0003 | t0003 | g0059 | AFR | GWD | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG02630 | hp1 | a0001 | c0001 | t0009 | g0017 | AFR | GWD | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG02630 | hp2 | a0003 | c0003 | t0003 | g0012 | AFR | GWD | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG02647 | hp1 | a0003 | c0003 | t0007 | g0153 | AFR | GWD | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG02647 | hp2 | a0002 | c0002 | t0011 | g0053 | AFR | GWD | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG02683 | hp1 | a0002 | c0002 | t0014 | g0175 | SAS | PJL | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG02683 | hp2 | a0009 | c0009 | t0003 | g0109 | SAS | PJL | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0032 | SAS | PJL | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG02698 | hp2 | a0002 | c0002 | t0014 | g0176 | SAS | PJL | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG02717 | hp1 | a0002 | c0002 | t0002 | g0006 | AFR | GWD | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG02717 | hp2 | a0005 | c0005 | t0010 | g0057 | AFR | GWD | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG02723 | hp1 | a0003 | c0003 | t0003 | g0012 | AFR | GWD | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG02723 | hp2 | a0002 | c0002 | t0002 | g0013 | AFR | GWD | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG02735 | hp1 | a0002 | c0002 | t0014 | g0174 | SAS | PJL | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG02735 | hp2 | a0002 | c0002 | t0002 | g0135 | SAS | PJL | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG02738 | hp1 | a0004 | c0004 | t0005 | g0049 | SAS | PJL | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG02738 | hp2 | a0016 | c0019 | t0003 | g0108 | SAS | PJL | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG02809 | hp1 | a0005 | c0005 | t0011 | g0172 | AFR | GWD | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG02809 | hp2 | a0008 | c0010 | t0008 | g0169 | AFR | GWD | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG02818 | hp1 | a0002 | c0002 | t0002 | g0013 | AFR | GWD | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG02818 | hp2 | a0006 | c0006 | t0012 | g0138 | AFR | GWD | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG02886 | hp1 | a0003 | c0003 | t0003 | g0015 | AFR | GWD | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG02886 | hp2 | a0003 | c0003 | t0007 | g0024 | AFR | GWD | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG02895 | hp1 | a0003 | c0003 | t0007 | g0146 | AFR | GWD | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG02895 | hp2 | a0002 | c0002 | t0002 | g0013 | AFR | GWD | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG02896 | hp1 | a0003 | c0003 | t0007 | g0024 | AFR | GWD | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG02896 | hp2 | a0002 | c0002 | t0002 | g0006 | AFR | GWD | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG02897 | hp1 | a0002 | c0002 | t0002 | g0013 | AFR | GWD | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG02897 | hp2 | a0003 | c0003 | t0007 | g0024 | AFR | GWD | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG02922 | hp1 | a0002 | c0002 | t0011 | g0053 | AFR | ESN | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG02922 | hp2 | a0006 | c0006 | t0012 | g0044 | AFR | ESN | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG02965 | hp1 | a0003 | c0003 | t0007 | g0047 | AFR | ESN | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG02965 | hp2 | a0006 | c0006 | t0015 | g0026 | AFR | ESN | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG02970 | hp1 | a0005 | c0005 | t0031 | g0158 | AFR | ESN | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG02970 | hp2 | a0010 | c0011 | t0034 | g0161 | AFR | ESN | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG02976 | hp1 | a0002 | c0002 | t0002 | g0006 | AFR | ESN | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG02976 | hp2 | a0002 | c0002 | t0002 | g0027 | AFR | ESN | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG03017 | hp1 | a0002 | c0002 | t0002 | g0125 | SAS | PJL | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG03041 | hp1 | a0002 | c0002 | t0002 | g0143 | AFR | GWD | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG03041 | hp2 | a0003 | c0003 | t0003 | g0040 | AFR | GWD | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG03098 | hp1 | a0002 | c0002 | t0002 | g0006 | AFR | MSL | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG03098 | hp2 | a0003 | c0003 | t0007 | g0147 | AFR | MSL | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG03130 | hp1 | a0005 | c0005 | t0018 | g0157 | AFR | ESN | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG03130 | hp2 | a0005 | c0005 | t0011 | g0166 | AFR | ESN | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG03139 | hp1 | a0008 | c0010 | t0008 | g0170 | AFR | ESN | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG03139 | hp2 | a0003 | c0003 | t0003 | g0061 | AFR | ESN | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG03195 | hp1 | a0003 | c0003 | t0003 | g0110 | AFR | ESN | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG03195 | hp2 | a0006 | c0006 | t0016 | g0025 | AFR | ESN | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG03209 | hp1 | a0005 | c0005 | t0010 | g0016 | AFR | MSL | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG03209 | hp2 | a0017 | c0025 | t0004 | g0122 | AFR | MSL | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | MSL | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG03225 | hp2 | a0002 | c0002 | t0002 | g0013 | AFR | MSL | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG03239 | hp2 | a0002 | c0002 | t0014 | g0173 | SAS | PJL | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG03453 | hp1 | a0006 | c0006 | t0032 | g0164 | AFR | MSL | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG03453 | hp2 | a0010 | c0011 | t0004 | g0045 | AFR | MSL | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG03486 | hp1 | a0002 | c0002 | t0002 | g0142 | AFR | MSL | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG03486 | hp2 | a0003 | c0003 | t0007 | g0050 | AFR | MSL | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG03490 | hp1 | a0003 | c0003 | t0003 | g0039 | SAS | PJL | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG03491 | hp2 | a0003 | c0003 | t0003 | g0005 | SAS | PJL | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | ESN | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG03516 | hp2 | a0003 | c0003 | t0003 | g0102 | AFR | ESN | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG03540 | hp1 | a0002 | c0002 | t0002 | g0013 | AFR | GWD | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG03540 | hp2 | a0005 | c0005 | t0010 | g0056 | AFR | GWD | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG03579 | hp1 | a0003 | c0003 | t0003 | g0012 | AFR | MSL | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG03579 | hp2 | a0005 | c0005 | t0011 | g0167 | AFR | MSL | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG03654 | hp2 | a0004 | c0004 | t0005 | g0048 | SAS | PJL | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG03669 | hp1 | a0002 | c0024 | t0002 | g0133 | SAS | PJL | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG03669 | hp2 | a0004 | c0007 | t0004 | g0084 | SAS | PJL | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG03688 | hp1 | a0003 | c0003 | t0003 | g0105 | SAS | STU | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG03688 | hp2 | a0001 | c0001 | t0023 | g0086 | SAS | STU | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0077 | SAS | PJL | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0081 | SAS | BEB | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG03831 | hp2 | a0001 | c0001 | t0011 | g0162 | SAS | BEB | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG03834 | hp1 | a0002 | c0002 | t0002 | g0002 | SAS | BEB | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG03834 | hp2 | a0004 | c0004 | t0005 | g0049 | SAS | BEB | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG03942 | hp1 | a0003 | c0003 | t0008 | g0163 | SAS | BEB | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | BEB | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0073 | SAS | STU | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG04204 | hp2 | a0002 | c0002 | t0002 | g0130 | SAS | STU | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG04228 | hp2 | a0003 | c0003 | t0003 | g0104 | SAS | STU | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| NA18522 | hp1 | a0003 | c0003 | t0003 | g0040 | AFR | YRI | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| NA18522 | hp2 | a0003 | c0003 | t0003 | g0015 | AFR | YRI | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| NA18612 | hp1 | a0004 | c0004 | t0005 | g0004 | EAS | CHB | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHB | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| NA18906 | hp1 | a0003 | c0003 | t0003 | g0012 | AFR | YRI | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| NA18906 | hp2 | a0002 | c0002 | t0002 | g0006 | AFR | YRI | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| NA18939 | hp2 | a0001 | c0001 | t0036 | g0179 | EAS | JPT | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| NA18943 | hp1 | a0001 | c0001 | t0006 | g0014 | EAS | JPT | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| NA18943 | hp2 | a0001 | c0001 | t0022 | g0069 | EAS | JPT | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| NA18944 | hp1 | a0004 | c0004 | t0005 | g0004 | EAS | JPT | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| NA18947 | hp2 | a0004 | c0004 | t0005 | g0004 | EAS | JPT | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| NA18950 | hp2 | a0004 | c0004 | t0005 | g0004 | EAS | JPT | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| NA18951 | hp1 | a0001 | c0001 | t0006 | g0019 | EAS | JPT | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| NA18954 | hp1 | a0001 | c0016 | t0029 | g0150 | EAS | JPT | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| NA18959 | hp1 | a0001 | c0001 | t0021 | g0072 | EAS | JPT | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| NA18961 | hp2 | a0001 | c0001 | t0024 | g0134 | EAS | JPT | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| NA18962 | hp2 | a0004 | c0004 | t0005 | g0004 | EAS | JPT | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| NA18963 | hp2 | a0001 | c0001 | t0006 | g0181 | EAS | JPT | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| NA18967 | hp1 | a0001 | c0001 | t0006 | g0054 | EAS | JPT | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| NA18970 | hp1 | a0004 | c0004 | t0004 | g0010 | EAS | JPT | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| NA18970 | hp2 | a0001 | c0001 | t0006 | g0055 | EAS | JPT | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| NA18971 | hp1 | a0001 | c0001 | t0006 | g0019 | EAS | JPT | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| NA18975 | hp2 | a0001 | c0001 | t0006 | g0014 | EAS | JPT | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| NA18980 | hp1 | a0004 | c0004 | t0004 | g0022 | EAS | JPT | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| NA18983 | hp2 | a0001 | c0001 | t0026 | g0145 | EAS | JPT | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| NA18990 | hp1 | a0004 | c0007 | t0004 | g0080 | EAS | JPT | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| NA18990 | hp2 | a0001 | c0001 | t0006 | g0014 | EAS | JPT | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| NA18991 | hp2 | a0004 | c0004 | t0004 | g0095 | EAS | JPT | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| NA18993 | hp2 | a0001 | c0001 | t0006 | g0180 | EAS | JPT | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| NA18998 | hp2 | a0004 | c0004 | t0005 | g0023 | EAS | JPT | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| NA18999 | hp2 | a0018 | c0015 | t0001 | g0063 | EAS | JPT | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| NA19004 | hp1 | a0004 | c0007 | t0004 | g0041 | EAS | JPT | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| NA19009 | hp2 | a0004 | c0004 | t0005 | g0004 | EAS | JPT | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| NA19010 | hp2 | a0004 | c0004 | t0005 | g0004 | EAS | JPT | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| NA19012 | hp1 | a0001 | c0001 | t0006 | g0054 | EAS | JPT | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| NA19012 | hp2 | a0001 | c0001 | t0006 | g0182 | EAS | JPT | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| NA19030 | hp1 | a0003 | c0003 | t0003 | g0012 | AFR | LWK | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| NA19030 | hp2 | a0002 | c0002 | t0033 | g0165 | AFR | LWK | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| NA19043 | hp1 | a0006 | c0006 | t0015 | g0026 | AFR | LWK | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| NA19043 | hp2 | a0009 | c0009 | t0003 | g0107 | AFR | LWK | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| NA19057 | hp2 | a0001 | c0001 | t0006 | g0014 | EAS | JPT | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| NA19060 | hp1 | a0004 | c0004 | t0005 | g0023 | EAS | JPT | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| NA19064 | hp1 | a0004 | c0004 | t0005 | g0004 | EAS | JPT | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| NA19066 | hp2 | a0004 | c0004 | t0004 | g0098 | EAS | JPT | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| NA19070 | hp1 | a0004 | c0004 | t0004 | g0093 | EAS | JPT | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| NA19070 | hp2 | a0004 | c0004 | t0004 | g0022 | EAS | JPT | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| NA19074 | hp1 | a0004 | c0004 | t0004 | g0010 | EAS | JPT | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| NA19083 | hp1 | a0001 | c0001 | t0006 | g0055 | EAS | JPT | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| NA19086 | hp1 | a0001 | c0001 | t0006 | g0178 | EAS | JPT | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| NA19086 | hp2 | a0004 | c0004 | t0004 | g0100 | EAS | JPT | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| NA19240 | hp1 | a0002 | c0002 | t0002 | g0144 | AFR | YRI | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| NA19240 | hp2 | a0004 | c0004 | t0005 | g0048 | AFR | YRI | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | ASW | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| NA20129 | hp2 | a0007 | c0008 | t0013 | g0113 | AFR | ASW | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| NA20752 | hp1 | a0002 | c0002 | t0002 | g0126 | EUR | TSI | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| NA20752 | hp2 | a0003 | c0003 | t0003 | g0039 | EUR | TSI | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| NA20905 | hp1 | a0002 | c0002 | t0002 | g0002 | SAS | GIH | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| NA20905 | hp2 | a0005 | c0005 | t0001 | g0087 | SAS | GIH | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG01123 | hp1 | a0004 | c0012 | t0004 | g0094 | AMR | CLM | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG01123 | hp2 | a0002 | c0002 | t0002 | g0002 | AMR | CLM | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG02109 | hp1 | a0010 | c0011 | t0004 | g0045 | AFR | ACB | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG02109 | hp2 | a0003 | c0003 | t0003 | g0101 | AFR | ACB | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG02486 | hp1 | a0002 | c0002 | t0002 | g0137 | AFR | ACB | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG02486 | hp2 | a0006 | c0006 | t0016 | g0025 | AFR | ACB | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG02559 | hp1 | a0003 | c0003 | t0003 | g0114 | AFR | ACB | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG02559 | hp2 | a0003 | c0003 | t0003 | g0005 | AFR | ACB | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG03471 | hp1 | a0006 | c0006 | t0027 | g0149 | AFR | MSL | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG03471 | hp2 | a0005 | c0005 | t0010 | g0016 | AFR | MSL | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG06807 | hp1 | a0003 | c0003 | t0007 | g0047 | AFR | USA | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| HG06807 | hp2 | a0002 | c0002 | t0002 | g0006 | AFR | USA | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | USA | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| NA20300 | hp2 | a0002 | c0002 | t0030 | g0148 | AFR | USA | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| NA21309 | hp1 | a0002 | c0002 | t0002 | g0141 | AFR | LWK | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| NA21309 | hp2 | a0007 | c0008 | t0013 | g0037 | AFR | LWK | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| homoSapiens | chm13v2 | a0002 | c0002 | t0002 | g0127 | REF | REF | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| homoSapiens | grch38p0 | a0004 | c0004 | t0004 | g0022 | REF | REF | FAM131C_chr1_16052769_16078651 | FAM131C | chr1 | 16052769 | 16078651 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:16058547 | G | A | 2 | a0012 a0018 |
2 | HG00735.hp2 NA18999.hp2 |
missense_variant | MODERATE | c.733C>T | p.Arg245Trp | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 7/7 | 942/1720 | 733/843 | 245/280 | chr1 | 16058547 | |||
| chr1:16058635 | G | T | 1 | a0007 | 5 | HG01884.hp2 HG02257.hp1 HG02622.hp1 others(2): Show |
missense_variant | MODERATE | c.645C>A | p.Ser215Arg | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 7/7 | 854/1720 | 645/843 | 215/280 | chr1 | 16058635 | |||
| chr1:16058636 | C | A | 8 | a0003 a0006 a0008 others(5): Show |
79 | HG00323.hp2 HG00639.hp1 HG00642.hp1 others(76): Show |
missense_variant | MODERATE | c.644G>T | p.Ser215Ile | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 7/7 | 853/1720 | 644/843 | 215/280 | chr1 | 16058636 | |||
| chr1:16059496 | T | C | 1 | a0007 | 5 | HG01884.hp2 HG02257.hp1 HG02622.hp1 others(2): Show |
missense_variant&splice_region_variant | MODERATE | c.560A>G | p.Gln187Arg | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 6/7 | 769/1720 | 560/843 | 187/280 | chr1 | 16059496 | |||
| chr1:16059548 | C | G | 2 | a0009 a0016 |
4 | HG01515.hp2 HG02683.hp2 HG02738.hp2 others(1): Show |
missense_variant | MODERATE | c.508G>C | p.Asp170His | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 6/7 | 717/1720 | 508/843 | 170/280 | chr1 | 16059548 | |||
| chr1:16059890 | G | T | 1 | a0015 | 1 | HG01978.hp2 | missense_variant | MODERATE | c.430C>A | p.Arg144Ser | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 5/7 | 639/1720 | 430/843 | 144/280 | chr1 | 16059890 | |||
| chr1:16059896 | C | T | 1 | a0015 | 1 | HG01978.hp2 | missense_variant | MODERATE | c.424G>A | p.Glu142Lys | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 5/7 | 633/1720 | 424/843 | 142/280 | chr1 | 16059896 | |||
| chr1:16059920 | C | T | 1 | a0014 | 1 | HG01361.hp2 | missense_variant | MODERATE | c.400G>A | p.Glu134Lys | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 5/7 | 609/1720 | 400/843 | 134/280 | chr1 | 16059920 | |||
| chr1:16059952 | G | C | 15 | a0001 a0002 a0003 others(12): Show |
330 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): Show |
missense_variant | MODERATE | c.368C>G | p.Pro123Arg | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 5/7 | 577/1720 | 368/843 | 123/280 | chr1 | 16059952 | |||
| chr1:16060000 | C | T | 3 | a0001 a0011 a0018 |
164 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(161): Show |
missense_variant | MODERATE | c.320G>A | p.Arg107Gln | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 5/7 | 529/1720 | 320/843 | 107/280 | chr1 | 16060000 | |||
| chr1:16062107 | G | A | 2 | a0013 a0016 |
2 | HG01106.hp1 HG02738.hp2 |
missense_variant | MODERATE | c.260C>T | p.Ser87Phe | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 4/7 | 469/1720 | 260/843 | 87/280 | chr1 | 16062107 | |||
| chr1:16062147 | G | A | 1 | a0013 | 1 | HG01106.hp1 | missense_variant | MODERATE | c.220C>T | p.Arg74Cys | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 4/7 | 429/1720 | 220/843 | 74/280 | chr1 | 16062147 | |||
| chr1:16062168 | A | G | 1 | a0008 | 3 | HG00642.hp1 HG02809.hp2 HG03139.hp1 |
missense_variant | MODERATE | c.199T>C | p.Tyr67His | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 4/7 | 408/1720 | 199/843 | 67/280 | chr1 | 16062168 | |||
| chr1:16062190 | C | A | 1 | a0011 | 1 | HG00642.hp2 | missense_variant&splice_region_variant | MODERATE | c.177G>T | p.Arg59Ser | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 4/7 | 386/1720 | 177/843 | 59/280 | chr1 | 16062190 | |||
| chr1:16062531 | T | C | 7 | a0002 a0006 a0008 others(4): Show |
87 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(84): Show |
missense_variant | MODERATE | c.142A>G | p.Lys48Glu | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 3/7 | 351/1720 | 142/843 | 48/280 | chr1 | 16062531 | |||
| chr1:16063586 | G | A | 1 | a0017 | 1 | HG03209.hp2 | missense_variant | MODERATE | c.73C>T | p.Pro25Ser | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 2/7 | 282/1720 | 73/843 | 25/280 | chr1 | 16063586 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:16058680 | G | A | 11 | a0001c0001 a0001c0016 a0002c0002 others(8): Show |
252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
synonymous_variant | LOW | c.600C>T | p.Ser200Ser | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 7/7 | 809/1720 | 600/843 | 200/280 | chr1 | 16058680 | |||
| chr1:16058689 | G | A | 1 | a0004c0012 | 1 | HG01123.hp1 | synonymous_variant | LOW | c.591C>T | p.Ser197Ser | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 7/7 | 800/1720 | 591/843 | 197/280 | chr1 | 16058689 | |||
| chr1:16059513 | T | C | 10 | a0001c0001 a0001c0016 a0002c0002 others(7): Show |
251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
synonymous_variant | LOW | c.543A>G | p.Gln181Gln | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 6/7 | 752/1720 | 543/843 | 181/280 | chr1 | 16059513 | |||
| chr1:16059546 | G | A | 1 | a0001c0016 | 1 | NA18954.hp1 | synonymous_variant | LOW | c.510C>T | p.Asp170Asp | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 6/7 | 719/1720 | 510/843 | 170/280 | chr1 | 16059546 | |||
| chr1:16059891 | C | G | 1 | a0015c0023 | 1 | HG01978.hp2 | synonymous_variant | LOW | c.429G>C | p.Leu143Leu | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 5/7 | 638/1720 | 429/843 | 143/280 | chr1 | 16059891 | |||
| chr1:16059900 | C | T | 1 | a0003c0018 | 1 | HG01891.hp2 | synonymous_variant | LOW | c.420G>A | p.Pro140Pro | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 5/7 | 629/1720 | 420/843 | 140/280 | chr1 | 16059900 | |||
| chr1:16059921 | G | A | 9 | a0001c0001 a0001c0016 a0002c0002 others(6): Show |
250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
synonymous_variant | LOW | c.399C>T | p.Asp133Asp | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 5/7 | 608/1720 | 399/843 | 133/280 | chr1 | 16059921 | |||
| chr1:16062151 | T | C | 16 | a0001c0001 a0001c0016 a0002c0002 others(13): Show |
318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
synonymous_variant | LOW | c.216A>G | p.Arg72Arg | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 4/7 | 425/1720 | 216/843 | 72/280 | chr1 | 16062151 | |||
| chr1:16062532 | G | A | 1 | a0002c0024 | 1 | HG03669.hp1 | splice_region_variant&synonymous_variant | LOW | c.141C>T | p.Asp47Asp | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 3/7 | 350/1720 | 141/843 | 47/280 | chr1 | 16062532 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:16057782 | C | T | 1 | a0001c0001t0022 | 1 | NA18943.hp2 | 3_prime_UTR_variant | MODIFIER | c.*655G>A | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 7/7 | 655 | chr1 | 16057782 | ||||||
| chr1:16057838 | G | T | 1 | a0001c0001t0009 | 7 | HG00140.hp1 HG01168.hp2 HG01255.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*599C>A | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 7/7 | 599 | chr1 | 16057838 | ||||||
| chr1:16057857 | G | C | 1 | a0002c0002t0033 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*580C>G | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 7/7 | 580 | chr1 | 16057857 | ||||||
| chr1:16057858 | T | C | 31 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0009 others(28): Show |
251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
3_prime_UTR_variant | MODIFIER | c.*579A>G | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 7/7 | 579 | chr1 | 16057858 | ||||||
| chr1:16057859 | G | A | 1 | a0001c0001t0023 | 1 | HG03688.hp2 | 3_prime_UTR_variant | MODIFIER | c.*578C>T | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 7/7 | 578 | chr1 | 16057859 | ||||||
| chr1:16057869 | G | A | 1 | a0001c0001t0024 | 1 | NA18961.hp2 | 3_prime_UTR_variant | MODIFIER | c.*568C>T | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 7/7 | 568 | chr1 | 16057869 | ||||||
| chr1:16057886 | G | T | 1 | a0007c0008t0013 | 4 | HG01884.hp2 HG02257.hp1 NA20129.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*551C>A | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 7/7 | 551 | chr1 | 16057886 | ||||||
| chr1:16058004 | C | A | 26 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0009 others(23): Show |
237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
3_prime_UTR_variant | MODIFIER | c.*433G>T | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 7/7 | 433 | chr1 | 16058004 | ||||||
| chr1:16058161 | G | T | 48 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0009 others(45): Show |
329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
3_prime_UTR_variant | MODIFIER | c.*276C>A | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 7/7 | 276 | chr1 | 16058161 | ||||||
| chr1:16058263 | C | T | 3 | a0001c0001t0017 a0001c0001t0021 a0001c0001t0036 |
4 | HG02015.hp2 HG02040.hp2 NA18939.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*174G>A | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 7/7 | 174 | chr1 | 16058263 | ||||||
| chr1:16058288 | C | T | 1 | a0001c0001t0020 | 1 | HG00738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*149G>A | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 7/7 | 149 | chr1 | 16058288 | ||||||
| chr1:16058289 | A | G | 36 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0009 others(33): Show |
260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
3_prime_UTR_variant | MODIFIER | c.*148T>C | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 7/7 | 148 | chr1 | 16058289 | ||||||
| chr1:16058306 | C | T | 29 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0009 others(26): Show |
194 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(191): Show |
3_prime_UTR_variant | MODIFIER | c.*131G>A | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 7/7 | 131 | chr1 | 16058306 | ||||||
| chr1:16058340 | G | GATGCCCT others(23): Show |
1 | a0002c0002t0019 | 1 | HG02258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*67_*96dupATCTGGAC others(22): Show |
FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 7/7 | 96 | chr1 | 16058340 | ||||||
| chr1:16058348 | G | C | 8 | a0003c0003t0003 a0003c0003t0007 a0003c0013t0035 others(5): Show |
58 | HG00639.hp1 HG00738.hp2 HG01069.hp2 others(55): Show |
3_prime_UTR_variant | MODIFIER | c.*89C>G | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 7/7 | 89 | chr1 | 16058348 | ||||||
| chr1:16058359 | C | T | 1 | a0005c0005t0018 | 2 | HG01243.hp2 HG03130.hp1 |
3_prime_UTR_variant | MODIFIER | c.*78G>A | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 7/7 | 78 | chr1 | 16058359 | ||||||
| chr1:16073475 | G | A | 1 | a0001c0001t0026 | 1 | NA18983.hp2 | 5_prime_UTR_variant | MODIFIER | c.-33C>T | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 1/7 | 33 | chr1 | 16073475 | ||||||
| chr1:16073509 | C | A | 7 | a0001c0016t0029 a0002c0002t0030 a0003c0003t0007 others(4): Show |
35 | HG00438.hp2 HG01106.hp2 HG01256.hp1 others(32): Show |
5_prime_UTR_variant | MODIFIER | c.-67G>T | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 1/7 | 67 | chr1 | 16073509 | ||||||
| chr1:16073515 | C | T | 2 | a0005c0005t0018 a0005c0005t0031 |
3 | HG01243.hp2 HG02970.hp1 HG03130.hp1 |
5_prime_UTR_variant | MODIFIER | c.-73G>A | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 1/7 | 73 | chr1 | 16073515 | ||||||
| chr1:16073545 | G | C | 12 | a0001c0001t0011 a0002c0002t0011 a0002c0002t0033 others(9): Show |
22 | HG00323.hp2 HG00642.hp1 HG01167.hp1 others(19): Show |
5_prime_UTR_variant | MODIFIER | c.-103C>G | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 1/7 | 103 | chr1 | 16073545 | ||||||
| chr1:16073552 | C | T | 1 | a0005c0005t0010 | 6 | HG02280.hp1 HG02451.hp1 HG02717.hp2 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-110G>A | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 1/7 | 110 | chr1 | 16073552 | ||||||
| chr1:16073577 | G | C | 1 | a0002c0002t0014 | 4 | HG02683.hp1 HG02698.hp2 HG02735.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-135C>G | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 1/7 | 135 | chr1 | 16073577 | ||||||
| chr1:16073597 | T | C | 2 | a0001c0001t0006 a0001c0001t0036 |
20 | HG00408.hp1 HG00597.hp1 HG02074.hp2 others(17): Show |
5_prime_UTR_variant | MODIFIER | c.-155A>G | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 1/7 | 155 | chr1 | 16073597 | ||||||
| chr1:16073598 | C | G | 2 | a0006c0006t0015 a0006c0006t0016 |
4 | HG02486.hp2 HG02965.hp2 HG03195.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-156G>C | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 1/7 | 156 | chr1 | 16073598 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:16058726 | G | C | 9 | a0003c0003t0003g0012 a0003c0003t0003g0038 a0003c0003t0003g0110 others(6): Show |
18 | HG01069.hp2 HG01071.hp1 HG01106.hp2 others(15): Show |
intron_variant | MODIFIER | c.563-9C>G | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 6/6 | chr1 | 16058726 | |||||||
| chr1:16058750 | G | A | 1 | a0004c0004t0005g0049 | 2 | HG02738.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.563-33C>T | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 6/6 | chr1 | 16058750 | |||||||
| chr1:16058753 | C | T | 1 | a0004c0012t0004g0094 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.563-36G>A | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 6/6 | chr1 | 16058753 | |||||||
| chr1:16058755 | A | G | 111 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(108): Show |
252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.563-38T>C | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 6/6 | chr1 | 16058755 | |||||||
| chr1:16058769 | G | GCCCT | 110 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(107): Show |
251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.563-56_563-53dupAG others(2): Show |
FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 6/6 | chr1 | 16058769 | |||||||
| chr1:16058769 | G | T | 1 | a0013c0020t0003g0116 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.563-52C>A | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 6/6 | chr1 | 16058769 | |||||||
| chr1:16058828 | A | G | 110 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(107): Show |
251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.563-111T>C | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 6/6 | chr1 | 16058828 | |||||||
| chr1:16058835 | G | T | 110 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(107): Show |
251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.563-118C>A | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 6/6 | chr1 | 16058835 | |||||||
| chr1:16059092 | G | A | 71 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(68): Show |
173 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(170): Show |
intron_variant | MODIFIER | c.563-375C>T | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 6/6 | chr1 | 16059092 | |||||||
| chr1:16059117 | G | A | 35 | a0003c0003t0003g0005 a0003c0003t0003g0012 a0003c0003t0003g0015 others(32): Show |
62 | HG00323.hp2 HG00639.hp1 HG00738.hp2 others(59): Show |
intron_variant | MODIFIER | c.562+377C>T | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 6/6 | chr1 | 16059117 | |||||||
| chr1:16059203 | A | G | 162 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(159): Show |
334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.562+291T>C | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 6/6 | chr1 | 16059203 | |||||||
| chr1:16059223 | C | G | 2 | a0002c0002t0011g0053 a0002c0002t0033g0165 |
3 | HG02647.hp2 HG02922.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.562+271G>C | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 6/6 | chr1 | 16059223 | |||||||
| chr1:16059243 | GC | G | 110 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(107): Show |
251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.562+250delG | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 6/6 | chr1 | 16059243 | |||||||
| chr1:16059273 | G | A | 64 | a0003c0003t0003g0005 a0003c0003t0003g0012 a0003c0003t0003g0015 others(61): Show |
103 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(100): Show |
intron_variant | MODIFIER | c.562+221C>T | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 6/6 | chr1 | 16059273 | |||||||
| chr1:16059289 | C | A | 1 | a0001c0001t0001g0099 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.562+205G>T | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 6/6 | chr1 | 16059289 | |||||||
| chr1:16059302 | C | G | 113 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(110): Show |
255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.562+192G>C | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 6/6 | chr1 | 16059302 | |||||||
| chr1:16059310 | C | T | 2 | a0002c0002t0011g0053 a0002c0002t0033g0165 |
3 | HG02647.hp2 HG02922.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.562+184G>A | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 6/6 | chr1 | 16059310 | |||||||
| chr1:16059320 | G | A | 31 | a0002c0002t0002g0002 a0002c0002t0002g0006 a0002c0002t0002g0013 others(28): Show |
66 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.562+174C>T | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 6/6 | chr1 | 16059320 | |||||||
| chr1:16059379 | T | C | 3 | a0001c0001t0026g0145 a0002c0002t0011g0053 a0002c0002t0033g0165 |
4 | HG02647.hp2 HG02922.hp1 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.562+115A>G | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 6/6 | chr1 | 16059379 | |||||||
| chr1:16059432 | G | A | 1 | a0001c0001t0026g0145 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.562+62C>T | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 6/6 | chr1 | 16059432 | |||||||
| chr1:16059436 | C | G | 1 | a0001c0001t0026g0145 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.562+58G>C | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 6/6 | chr1 | 16059436 | |||||||
| chr1:16059441 | C | T | 1 | a0001c0001t0026g0145 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.562+53G>A | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 6/6 | chr1 | 16059441 | |||||||
| chr1:16059444 | A | C | 1 | a0001c0001t0026g0145 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.562+50T>G | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 6/6 | chr1 | 16059444 | |||||||
| chr1:16059445 | A | G | 1 | a0001c0001t0026g0145 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.562+49T>C | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 6/6 | chr1 | 16059445 | |||||||
| chr1:16059449 | G | C | 1 | a0001c0001t0026g0145 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.562+45C>G | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 6/6 | chr1 | 16059449 | |||||||
| chr1:16059469 | G | T | 1 | a0001c0001t0026g0145 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.562+25C>A | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 6/6 | chr1 | 16059469 | |||||||
| chr1:16059474 | C | G | 2 | a0001c0001t0001g0032 a0001c0001t0001g0081 |
3 | HG01358.hp1 HG02698.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.562+20G>C | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 6/6 | chr1 | 16059474 | |||||||
| chr1:16059485 | G | A | 109 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(106): Show |
250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.562+9C>T | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 6/6 | chr1 | 16059485 | |||||||
| chr1:16059651 | G | A | 1 | a0002c0002t0002g0141 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.452-47C>T | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 5/6 | chr1 | 16059651 | |||||||
| chr1:16059715 | A | C | 10 | a0002c0002t0002g0013 a0002c0002t0002g0117 a0002c0002t0002g0137 others(7): Show |
15 | HG01099.hp2 HG01175.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.452-111T>G | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 5/6 | chr1 | 16059715 | |||||||
| chr1:16059715 | A | G | 6 | a0003c0003t0003g0040 a0003c0003t0003g0102 a0003c0003t0003g0103 others(3): Show |
8 | HG02258.hp1 HG02895.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.452-111T>C | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 5/6 | chr1 | 16059715 | |||||||
| chr1:16059752 | T | C | 159 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(156): Show |
330 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): Show |
intron_variant | MODIFIER | c.451+117A>G | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 5/6 | chr1 | 16059752 | |||||||
| chr1:16059810 | G | GC | 110 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(107): Show |
251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.451+58dupG | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 5/6 | chr1 | 16059810 | |||||||
| chr1:16060125 | G | A | 11 | a0002c0002t0011g0053 a0002c0002t0033g0165 a0005c0005t0010g0016 others(8): Show |
16 | HG01243.hp2 HG01884.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.269-74C>T | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 4/6 | chr1 | 16060125 | |||||||
| chr1:16060142 | T | C | 2 | a0003c0003t0003g0059 a0003c0003t0003g0061 |
2 | HG02622.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.269-91A>G | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 4/6 | chr1 | 16060142 | |||||||
| chr1:16060161 | GCACCATG others(14): Show |
G | 68 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(65): Show |
169 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.269-131_269-111del others(21): Show |
FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 4/6 | chr1 | 16060161 | |||||||
| chr1:16060181 | GC | G | 42 | a0002c0002t0002g0002 a0002c0002t0002g0006 a0002c0002t0002g0013 others(39): Show |
82 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(79): Show |
intron_variant | MODIFIER | c.269-131delG | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 4/6 | chr1 | 16060181 | |||||||
| chr1:16060201 | G | A | 2 | a0002c0002t0002g0129 a0015c0023t0002g0128 |
2 | HG00099.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.269-150C>T | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 4/6 | chr1 | 16060201 | |||||||
| chr1:16060205 | G | A | 2 | a0002c0002t0011g0053 a0002c0002t0033g0165 |
3 | HG02647.hp2 HG02922.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.269-154C>T | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 4/6 | chr1 | 16060205 | |||||||
| chr1:16060225 | G | A | 68 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(65): Show |
169 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.269-174C>T | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 4/6 | chr1 | 16060225 | |||||||
| chr1:16060228 | C | T | 68 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(65): Show |
169 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.269-177G>A | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 4/6 | chr1 | 16060228 | |||||||
| chr1:16060239 | T | C | 110 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(107): Show |
251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.269-188A>G | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 4/6 | chr1 | 16060239 | |||||||
| chr1:16060265 | C | T | 68 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(65): Show |
169 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.269-214G>A | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 4/6 | chr1 | 16060265 | |||||||
| chr1:16060279 | C | T | 4 | a0001c0001t0001g0021 a0001c0001t0001g0029 a0001c0001t0001g0033 others(1): Show |
8 | HG01496.hp1 HG01993.hp2 NA18939.hp1 others(5): Show |
intron_variant | MODIFIER | c.269-228G>A | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 4/6 | chr1 | 16060279 | |||||||
| chr1:16060283 | T | C | 68 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(65): Show |
169 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.269-232A>G | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 4/6 | chr1 | 16060283 | |||||||
| chr1:16060288 | T | C | 68 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(65): Show |
169 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.269-237A>G | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 4/6 | chr1 | 16060288 | |||||||
| chr1:16060312 | A | G | 68 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(65): Show |
169 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.269-261T>C | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 4/6 | chr1 | 16060312 | |||||||
| chr1:16060351 | G | A | 42 | a0002c0002t0002g0002 a0002c0002t0002g0006 a0002c0002t0002g0013 others(39): Show |
82 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(79): Show |
intron_variant | MODIFIER | c.269-300C>T | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 4/6 | chr1 | 16060351 | |||||||
| chr1:16060360 | A | G | 68 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(65): Show |
169 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.269-309T>C | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 4/6 | chr1 | 16060360 | |||||||
| chr1:16060369 | C | T | 2 | a0001c0001t0001g0032 a0001c0001t0001g0081 |
3 | HG01358.hp1 HG02698.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.269-318G>A | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 4/6 | chr1 | 16060369 | |||||||
| chr1:16060433 | G | T | 91 | a0002c0002t0002g0002 a0002c0002t0002g0006 a0002c0002t0002g0013 others(88): Show |
161 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.269-382C>A | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 4/6 | chr1 | 16060433 | |||||||
| chr1:16060510 | C | CT | 68 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(65): Show |
169 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.269-460_269-459ins others(1): Show |
FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 4/6 | chr1 | 16060510 | |||||||
| chr1:16060511 | C | G | 68 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(65): Show |
169 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.269-460G>C | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 4/6 | chr1 | 16060511 | |||||||
| chr1:16060535 | C | T | 66 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(63): Show |
167 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(164): Show |
intron_variant | MODIFIER | c.269-484G>A | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 4/6 | chr1 | 16060535 | |||||||
| chr1:16060685 | G | A | 5 | a0003c0003t0012g0111 a0007c0008t0013g0037 a0007c0008t0013g0112 others(2): Show |
6 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.269-634C>T | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 4/6 | chr1 | 16060685 | |||||||
| chr1:16060724 | T | A | 159 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(156): Show |
330 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): Show |
intron_variant | MODIFIER | c.269-673A>T | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 4/6 | chr1 | 16060724 | |||||||
| chr1:16060736 | C | T | 1 | a0007c0014t0028g0154 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.269-685G>A | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 4/6 | chr1 | 16060736 | |||||||
| chr1:16060907 | C | G | 77 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(74): Show |
178 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(175): Show |
intron_variant | MODIFIER | c.269-856G>C | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 4/6 | chr1 | 16060907 | |||||||
| chr1:16060950 | A | G | 70 | a0001c0001t0001g0081 a0001c0001t0001g0083 a0001c0001t0009g0082 others(67): Show |
132 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.269-899T>C | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 4/6 | chr1 | 16060950 | |||||||
| chr1:16060953 | G | A | 8 | a0002c0002t0011g0053 a0002c0002t0033g0165 a0005c0005t0010g0016 others(5): Show |
12 | HG01243.hp2 HG02280.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.269-902C>T | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 4/6 | chr1 | 16060953 | |||||||
| chr1:16060961 | C | T | 1 | a0001c0001t0024g0134 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.269-910G>A | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 4/6 | chr1 | 16060961 | |||||||
| chr1:16060971 | G | A | 75 | a0002c0002t0002g0002 a0002c0002t0002g0006 a0002c0002t0002g0013 others(72): Show |
141 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(138): Show |
intron_variant | MODIFIER | c.269-920C>T | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 4/6 | chr1 | 16060971 | |||||||
| chr1:16060974 | A | G | 75 | a0002c0002t0002g0002 a0002c0002t0002g0006 a0002c0002t0002g0013 others(72): Show |
141 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(138): Show |
intron_variant | MODIFIER | c.269-923T>C | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 4/6 | chr1 | 16060974 | |||||||
| chr1:16061078 | G | A | 84 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(81): Show |
192 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(189): Show |
intron_variant | MODIFIER | c.268+1021C>T | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 4/6 | chr1 | 16061078 | |||||||
| chr1:16061134 | A | G | 30 | a0002c0002t0002g0002 a0002c0002t0002g0006 a0002c0002t0002g0013 others(27): Show |
65 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(62): Show |
intron_variant | MODIFIER | c.268+965T>C | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 4/6 | chr1 | 16061134 | |||||||
| chr1:16061286 | AG | A | 67 | a0001c0001t0001g0091 a0002c0002t0002g0002 a0002c0002t0002g0006 others(64): Show |
129 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.268+812delC | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 4/6 | chr1 | 16061286 | |||||||
| chr1:16061518 | C | T | 3 | a0003c0003t0008g0051 a0003c0003t0008g0052 a0003c0003t0008g0163 |
5 | HG00323.hp2 HG01167.hp1 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.268+581G>A | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 4/6 | chr1 | 16061518 | |||||||
| chr1:16061601 | G | A | 3 | a0003c0003t0008g0051 a0003c0003t0008g0052 a0003c0003t0008g0163 |
5 | HG00323.hp2 HG01167.hp1 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.268+498C>T | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 4/6 | chr1 | 16061601 | |||||||
| chr1:16061614 | G | C | 1 | a0002c0002t0002g0130 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.268+485C>G | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 4/6 | chr1 | 16061614 | |||||||
| chr1:16061744 | G | C | 10 | a0002c0002t0002g0013 a0002c0002t0002g0117 a0002c0002t0002g0137 others(7): Show |
15 | HG01099.hp2 HG01175.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.268+355C>G | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 4/6 | chr1 | 16061744 | |||||||
| chr1:16061757 | A | G | 1 | a0009c0009t0003g0106 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.268+342T>C | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 4/6 | chr1 | 16061757 | |||||||
| chr1:16061810 | A | C | 1 | a0001c0001t0009g0031 | 2 | HG01168.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.268+289T>G | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 4/6 | chr1 | 16061810 | |||||||
| chr1:16061834 | T | C | 13 | a0003c0003t0003g0012 a0003c0003t0003g0038 a0003c0003t0003g0110 others(10): Show |
23 | HG01069.hp2 HG01071.hp1 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.268+265A>G | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 4/6 | chr1 | 16061834 | |||||||
| chr1:16061972 | A | G | 8 | a0002c0002t0011g0053 a0002c0002t0033g0165 a0005c0005t0010g0016 others(5): Show |
12 | HG01243.hp2 HG02280.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.268+127T>C | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 4/6 | chr1 | 16061972 | |||||||
| chr1:16061979 | G | A | 30 | a0002c0002t0002g0002 a0002c0002t0002g0006 a0002c0002t0002g0013 others(27): Show |
65 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(62): Show |
intron_variant | MODIFIER | c.268+120C>T | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 4/6 | chr1 | 16061979 | |||||||
| chr1:16061990 | T | C | 72 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(69): Show |
174 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(171): Show |
intron_variant | MODIFIER | c.268+109A>G | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 4/6 | chr1 | 16061990 | |||||||
| chr1:16062039 | C | T | 30 | a0002c0002t0002g0002 a0002c0002t0002g0006 a0002c0002t0002g0013 others(27): Show |
65 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(62): Show |
intron_variant | MODIFIER | c.268+60G>A | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 4/6 | chr1 | 16062039 | |||||||
| chr1:16062061 | C | T | 102 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(99): Show |
240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.268+38G>A | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 4/6 | chr1 | 16062061 | |||||||
| chr1:16062070 | C | G | 70 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(67): Show |
172 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(169): Show |
intron_variant | MODIFIER | c.268+29G>C | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 4/6 | chr1 | 16062070 | |||||||
| chr1:16062085 | C | T | 31 | a0002c0002t0002g0002 a0002c0002t0002g0006 a0002c0002t0002g0013 others(28): Show |
67 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(64): Show |
intron_variant | MODIFIER | c.268+14G>A | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 4/6 | chr1 | 16062085 | |||||||
| chr1:16062214 | G | T | 112 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(109): Show |
242 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(239): Show |
intron_variant | MODIFIER | c.175-22C>A | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 3/6 | chr1 | 16062214 | |||||||
| chr1:16062242 | G | A | 40 | a0002c0002t0002g0002 a0002c0002t0002g0006 a0002c0002t0002g0013 others(37): Show |
78 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(75): Show |
intron_variant | MODIFIER | c.175-50C>T | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 3/6 | chr1 | 16062242 | |||||||
| chr1:16062261 | CACCCAT | C | 40 | a0003c0003t0003g0005 a0003c0003t0003g0012 a0003c0003t0003g0015 others(37): Show |
68 | HG00323.hp2 HG00639.hp1 HG00738.hp2 others(65): Show |
intron_variant | MODIFIER | c.175-75_175-70delAT others(4): Show |
FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 3/6 | chr1 | 16062261 | |||||||
| chr1:16062271 | C | T | 141 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(138): Show |
307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.175-79G>A | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 3/6 | chr1 | 16062271 | |||||||
| chr1:16062274 | C | T | 1 | a0005c0005t0010g0056 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.175-82G>A | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 3/6 | chr1 | 16062274 | |||||||
| chr1:16062288 | G | A | 2 | a0001c0001t0001g0070 a0001c0001t0001g0089 |
2 | NA18983.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.175-96C>T | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 3/6 | chr1 | 16062288 | |||||||
| chr1:16062357 | AC | A | 38 | a0002c0002t0002g0002 a0002c0002t0002g0006 a0002c0002t0002g0013 others(35): Show |
77 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(74): Show |
intron_variant | MODIFIER | c.174+141delG | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 3/6 | chr1 | 16062357 | |||||||
| chr1:16062380 | G | GC | 25 | a0002c0002t0033g0165 a0003c0003t0003g0015 a0003c0003t0003g0040 others(22): Show |
36 | HG00621.hp1 HG00639.hp1 HG01099.hp1 others(33): Show |
intron_variant | MODIFIER | c.174+118dupG | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 3/6 | chr1 | 16062380 | |||||||
| chr1:16062380 | G | GCC | 10 | a0003c0003t0003g0005 a0003c0003t0003g0103 a0003c0003t0007g0047 others(7): Show |
19 | HG00642.hp1 HG00738.hp2 HG01192.hp1 others(16): Show |
intron_variant | MODIFIER | c.174+117_174+118dup others(2): Show |
FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 3/6 | chr1 | 16062380 | |||||||
| chr1:16062380 | GC | G | 26 | a0001c0001t0001g0007 a0001c0001t0001g0065 a0001c0001t0001g0073 others(23): Show |
52 | HG00323.hp2 HG00741.hp2 HG01070.hp1 others(49): Show |
intron_variant | MODIFIER | c.174+118delG | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 3/6 | chr1 | 16062380 | |||||||
| chr1:16062380 | GCC | G | 75 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(72): Show |
184 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(181): Show |
intron_variant | MODIFIER | c.174+117_174+118del others(2): Show |
FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 3/6 | chr1 | 16062380 | |||||||
| chr1:16062384 | C | A | 1 | a0002c0002t0002g0132 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.174+115G>T | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 3/6 | chr1 | 16062384 | |||||||
| chr1:16062384 | C | T | 1 | a0001c0001t0001g0079 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.174+115G>A | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 3/6 | chr1 | 16062384 | |||||||
| chr1:16062386 | C | G | 1 | a0002c0002t0002g0124 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.174+113G>C | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 3/6 | chr1 | 16062386 | |||||||
| chr1:16062390 | C | T | 3 | a0001c0001t0017g0030 a0001c0001t0026g0145 a0001c0001t0036g0179 |
4 | HG02015.hp2 HG02040.hp2 NA18939.hp2 others(1): Show |
intron_variant | MODIFIER | c.174+109G>A | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 3/6 | chr1 | 16062390 | |||||||
| chr1:16062392 | C | T | 1 | a0002c0002t0002g0135 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.174+107G>A | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 3/6 | chr1 | 16062392 | |||||||
| chr1:16062409 | A | T | 31 | a0002c0002t0002g0002 a0002c0002t0002g0006 a0002c0002t0002g0013 others(28): Show |
67 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(64): Show |
intron_variant | MODIFIER | c.174+90T>A | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 3/6 | chr1 | 16062409 | |||||||
| chr1:16062414 | T | C | 32 | a0002c0002t0002g0002 a0002c0002t0002g0006 a0002c0002t0002g0013 others(29): Show |
68 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(65): Show |
intron_variant | MODIFIER | c.174+85A>G | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 3/6 | chr1 | 16062414 | |||||||
| chr1:16062449 | C | A | 1 | a0002c0002t0002g0144 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.174+50G>T | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 3/6 | chr1 | 16062449 | |||||||
| chr1:16062454 | T | C | 5 | a0003c0013t0035g0171 a0006c0006t0016g0025 a0008c0010t0008g0168 others(2): Show |
6 | HG00642.hp1 HG02486.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.174+45A>G | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 3/6 | chr1 | 16062454 | |||||||
| chr1:16062487 | A | T | 1 | a0012c0022t0025g0139 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.174+12T>A | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 3/6 | chr1 | 16062487 | |||||||
| chr1:16062541 | CAAGAG | C | 6 | a0005c0005t0010g0016 a0005c0005t0010g0056 a0005c0005t0010g0057 others(3): Show |
9 | HG01243.hp2 HG02280.hp1 HG02451.hp1 others(6): Show |
splice_region_variant&intron_variant | LOW | c.139-12_139-8delCTC others(2): Show |
FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 2/6 | chr1 | 16062541 | |||||||
| chr1:16062584 | A | G | 5 | a0001c0001t0001g0021 a0001c0001t0001g0078 a0006c0006t0012g0058 others(2): Show |
8 | HG02109.hp1 HG02572.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.139-50T>C | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 2/6 | chr1 | 16062584 | |||||||
| chr1:16062616 | G | A | 1 | a0004c0004t0004g0098 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.139-82C>T | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 2/6 | chr1 | 16062616 | |||||||
| chr1:16062623 | G | A | 38 | a0003c0003t0003g0005 a0003c0003t0003g0012 a0003c0003t0003g0015 others(35): Show |
66 | HG00323.hp2 HG00639.hp1 HG00738.hp2 others(63): Show |
intron_variant | MODIFIER | c.139-89C>T | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 2/6 | chr1 | 16062623 | |||||||
| chr1:16062640 | G | C | 3 | a0003c0003t0008g0051 a0003c0003t0008g0052 a0003c0003t0008g0163 |
5 | HG00323.hp2 HG01167.hp1 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.139-106C>G | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 2/6 | chr1 | 16062640 | |||||||
| chr1:16062645 | G | C | 21 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0097 others(18): Show |
27 | HG01167.hp2 HG01243.hp2 HG01981.hp2 others(24): Show |
intron_variant | MODIFIER | c.139-111C>G | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 2/6 | chr1 | 16062645 | |||||||
| chr1:16062646 | T | C | 21 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0097 others(18): Show |
27 | HG01167.hp2 HG01243.hp2 HG01981.hp2 others(24): Show |
intron_variant | MODIFIER | c.139-112A>G | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 2/6 | chr1 | 16062646 | |||||||
| chr1:16062654 | T | C | 15 | a0001c0001t0001g0028 a0001c0001t0001g0065 a0001c0001t0001g0066 others(12): Show |
19 | HG01069.hp2 HG01071.hp1 HG01167.hp2 others(16): Show |
intron_variant | MODIFIER | c.139-120A>G | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 2/6 | chr1 | 16062654 | |||||||
| chr1:16062694 | G | A | 1 | a0002c0002t0002g0117 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.139-160C>T | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 2/6 | chr1 | 16062694 | |||||||
| chr1:16062696 | C | A | 1 | a0002c0002t0002g0117 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.139-162G>T | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 2/6 | chr1 | 16062696 | |||||||
| chr1:16062713 | A | T | 19 | a0001c0001t0001g0074 a0002c0002t0002g0018 a0003c0003t0003g0012 others(16): Show |
31 | HG00140.hp2 HG00323.hp2 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.139-179T>A | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 2/6 | chr1 | 16062713 | |||||||
| chr1:16062739 | C | G | 2 | a0009c0009t0003g0109 a0012c0022t0025g0139 |
2 | HG00735.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.139-205G>C | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 2/6 | chr1 | 16062739 | |||||||
| chr1:16062744 | C | A | 2 | a0009c0009t0003g0109 a0012c0022t0025g0139 |
2 | HG00735.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.139-210G>T | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 2/6 | chr1 | 16062744 | |||||||
| chr1:16062745 | T | G | 2 | a0009c0009t0003g0109 a0012c0022t0025g0139 |
2 | HG00735.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.139-211A>C | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 2/6 | chr1 | 16062745 | |||||||
| chr1:16062747 | G | A | 2 | a0009c0009t0003g0109 a0012c0022t0025g0139 |
2 | HG00735.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.139-213C>T | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 2/6 | chr1 | 16062747 | |||||||
| chr1:16062793 | A | G | 32 | a0001c0001t0011g0162 a0003c0003t0003g0005 a0003c0003t0003g0012 others(29): Show |
57 | HG00323.hp2 HG00639.hp1 HG00738.hp2 others(54): Show |
intron_variant | MODIFIER | c.139-259T>C | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 2/6 | chr1 | 16062793 | |||||||
| chr1:16062867 | T | G | 8 | a0001c0001t0001g0073 a0002c0002t0011g0053 a0005c0005t0010g0016 others(5): Show |
12 | HG01243.hp2 HG02280.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.139-333A>C | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 2/6 | chr1 | 16062867 | |||||||
| chr1:16062879 | A | C | 1 | a0001c0001t0006g0054 | 2 | NA18967.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.139-345T>G | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 2/6 | chr1 | 16062879 | |||||||
| chr1:16062879 | A | T | 1 | a0002c0002t0002g0043 | 2 | HG00323.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.139-345T>A | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 2/6 | chr1 | 16062879 | |||||||
| chr1:16062880 | T | C | 12 | a0001c0001t0001g0011 a0001c0001t0001g0060 a0002c0002t0011g0053 others(9): Show |
21 | HG00558.hp2 HG01243.hp2 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.139-346A>G | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 2/6 | chr1 | 16062880 | |||||||
| chr1:16062895 | C | A | 2 | a0002c0002t0002g0006 a0002c0002t0002g0027 |
11 | HG01070.hp1 HG01071.hp2 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.139-361G>T | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 2/6 | chr1 | 16062895 | |||||||
| chr1:16062910 | G | A | 7 | a0002c0002t0002g0006 a0002c0002t0002g0027 a0002c0002t0002g0141 others(4): Show |
18 | HG00323.hp2 HG01070.hp1 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.139-376C>T | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 2/6 | chr1 | 16062910 | |||||||
| chr1:16062956 | C | T | 1 | a0001c0001t0001g0077 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.139-422G>A | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 2/6 | chr1 | 16062956 | |||||||
| chr1:16062957 | G | A | 2 | a0003c0003t0003g0059 a0003c0003t0003g0061 |
2 | HG02622.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.139-423C>T | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 2/6 | chr1 | 16062957 | |||||||
| chr1:16063017 | C | T | 8 | a0003c0003t0008g0051 a0003c0003t0008g0052 a0003c0003t0008g0163 others(5): Show |
10 | HG00323.hp2 HG01167.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.139-483G>A | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 2/6 | chr1 | 16063017 | |||||||
| chr1:16063018 | G | A | 8 | a0003c0003t0008g0051 a0003c0003t0008g0052 a0003c0003t0008g0163 others(5): Show |
10 | HG00323.hp2 HG01167.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.139-484C>T | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 2/6 | chr1 | 16063018 | |||||||
| chr1:16063043 | T | C | 8 | a0003c0003t0008g0051 a0003c0003t0008g0052 a0003c0003t0008g0163 others(5): Show |
10 | HG00323.hp2 HG01167.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.138+478A>G | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 2/6 | chr1 | 16063043 | |||||||
| chr1:16063045 | C | T | 8 | a0003c0003t0008g0051 a0003c0003t0008g0052 a0003c0003t0008g0163 others(5): Show |
10 | HG00323.hp2 HG01167.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.138+476G>A | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 2/6 | chr1 | 16063045 | |||||||
| chr1:16063048 | T | A | 8 | a0003c0003t0008g0051 a0003c0003t0008g0052 a0003c0003t0008g0163 others(5): Show |
10 | HG00323.hp2 HG01167.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.138+473A>T | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 2/6 | chr1 | 16063048 | |||||||
| chr1:16063157 | TAA | T | 23 | a0001c0001t0001g0046 a0002c0002t0002g0006 a0002c0002t0002g0013 others(20): Show |
40 | HG00323.hp2 HG01070.hp1 HG01071.hp2 others(37): Show |
intron_variant | MODIFIER | c.138+362_138+363del others(2): Show |
FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 2/6 | chr1 | 16063157 | |||||||
| chr1:16063182 | A | G | 12 | a0001c0001t0001g0046 a0002c0002t0002g0013 a0002c0002t0002g0117 others(9): Show |
18 | HG01099.hp2 HG01175.hp2 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.138+339T>C | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 2/6 | chr1 | 16063182 | |||||||
| chr1:16063200 | A | G | 1 | a0001c0001t0001g0008 | 7 | NA18951.hp2 NA18954.hp2 NA18969.hp2 others(4): Show |
intron_variant | MODIFIER | c.138+321T>C | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 2/6 | chr1 | 16063200 | |||||||
| chr1:16063208 | T | C | 23 | a0001c0001t0001g0046 a0002c0002t0002g0006 a0002c0002t0002g0013 others(20): Show |
40 | HG00323.hp2 HG01070.hp1 HG01071.hp2 others(37): Show |
intron_variant | MODIFIER | c.138+313A>G | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 2/6 | chr1 | 16063208 | |||||||
| chr1:16063283 | C | T | 8 | a0003c0003t0008g0051 a0003c0003t0008g0052 a0003c0003t0008g0163 others(5): Show |
10 | HG00323.hp2 HG01167.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.138+238G>A | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 2/6 | chr1 | 16063283 | |||||||
| chr1:16063305 | T | A | 8 | a0003c0003t0008g0051 a0003c0003t0008g0052 a0003c0003t0008g0163 others(5): Show |
10 | HG00323.hp2 HG01167.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.138+216A>T | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 2/6 | chr1 | 16063305 | |||||||
| chr1:16063332 | T | TCCCTGGA others(18): Show |
11 | a0003c0003t0008g0051 a0003c0003t0008g0052 a0003c0003t0008g0163 others(8): Show |
16 | HG00323.hp2 HG01167.hp1 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.138+164_138+188dup others(25): Show |
FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 2/6 | chr1 | 16063332 | |||||||
| chr1:16063456 | T | G | 1 | a0007c0008t0013g0113 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.138+65A>C | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 2/6 | chr1 | 16063456 | |||||||
| chr1:16063512 | G | C | 9 | a0002c0002t0011g0053 a0003c0003t0008g0051 a0003c0003t0008g0052 others(6): Show |
12 | HG00323.hp2 HG01167.hp1 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.138+9C>G | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 2/6 | chr1 | 16063512 | |||||||
| chr1:16063788 | G | A | 5 | a0006c0006t0012g0058 a0006c0006t0012g0138 a0010c0011t0004g0045 others(2): Show |
6 | HG00735.hp2 HG02109.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.23-152C>T | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 1/6 | chr1 | 16063788 | |||||||
| chr1:16063818 | C | G | 1 | a0001c0001t0001g0076 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.23-182G>C | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 1/6 | chr1 | 16063818 | |||||||
| chr1:16063824 | C | T | 13 | a0001c0001t0001g0046 a0002c0002t0002g0006 a0002c0002t0002g0013 others(10): Show |
28 | HG01070.hp1 HG01071.hp2 HG01099.hp2 others(25): Show |
intron_variant | MODIFIER | c.23-188G>A | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 1/6 | chr1 | 16063824 | |||||||
| chr1:16063841 | ATCT | A | 13 | a0001c0001t0001g0046 a0002c0002t0002g0006 a0002c0002t0002g0013 others(10): Show |
28 | HG01070.hp1 HG01071.hp2 HG01099.hp2 others(25): Show |
intron_variant | MODIFIER | c.23-208_23-206delAG others(1): Show |
FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 1/6 | chr1 | 16063841 | |||||||
| chr1:16063863 | T | G | 22 | a0001c0001t0001g0046 a0002c0002t0002g0006 a0002c0002t0002g0013 others(19): Show |
39 | HG00323.hp2 HG01070.hp1 HG01071.hp2 others(36): Show |
intron_variant | MODIFIER | c.23-227A>C | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 1/6 | chr1 | 16063863 | |||||||
| chr1:16064033 | C | T | 8 | a0003c0003t0008g0051 a0003c0003t0008g0052 a0003c0003t0008g0163 others(5): Show |
10 | HG00323.hp2 HG01167.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.23-397G>A | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 1/6 | chr1 | 16064033 | |||||||
| chr1:16064040 | G | A | 13 | a0001c0001t0001g0046 a0002c0002t0002g0006 a0002c0002t0002g0013 others(10): Show |
28 | HG01070.hp1 HG01071.hp2 HG01099.hp2 others(25): Show |
intron_variant | MODIFIER | c.23-404C>T | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 1/6 | chr1 | 16064040 | |||||||
| chr1:16064109 | G | T | 8 | a0003c0003t0008g0051 a0003c0003t0008g0052 a0003c0003t0008g0163 others(5): Show |
10 | HG00323.hp2 HG01167.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.23-473C>A | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 1/6 | chr1 | 16064109 | |||||||
| chr1:16064194 | G | C | 1 | a0003c0003t0003g0114 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.23-558C>G | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 1/6 | chr1 | 16064194 | |||||||
| chr1:16064242 | C | G | 1 | a0006c0006t0012g0044 | 2 | HG01167.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.23-606G>C | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 1/6 | chr1 | 16064242 | |||||||
| chr1:16064255 | A | C | 1 | a0014c0017t0003g0075 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.23-619T>G | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 1/6 | chr1 | 16064255 | |||||||
| chr1:16064318 | T | C | 56 | a0002c0002t0002g0002 a0002c0002t0002g0018 a0002c0002t0002g0043 others(53): Show |
102 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(99): Show |
intron_variant | MODIFIER | c.23-682A>G | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 1/6 | chr1 | 16064318 | |||||||
| chr1:16064371 | C | T | 1 | a0006c0006t0008g0160 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.23-735G>A | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 1/6 | chr1 | 16064371 | |||||||
| chr1:16064399 | G | A | 2 | a0001c0001t0001g0036 a0001c0001t0001g0099 |
3 | HG02523.hp1 NA18959.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.23-763C>T | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 1/6 | chr1 | 16064399 | |||||||
| chr1:16064400 | C | T | 3 | a0005c0005t0010g0016 a0005c0005t0010g0056 a0005c0005t0010g0057 |
6 | HG02280.hp1 HG02451.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.23-764G>A | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 1/6 | chr1 | 16064400 | |||||||
| chr1:16064468 | C | G | 1 | a0001c0001t0001g0074 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.23-832G>C | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 1/6 | chr1 | 16064468 | |||||||
| chr1:16064493 | G | A | 66 | a0002c0002t0002g0002 a0002c0002t0002g0018 a0002c0002t0002g0043 others(63): Show |
114 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(111): Show |
intron_variant | MODIFIER | c.23-857C>T | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 1/6 | chr1 | 16064493 | |||||||
| chr1:16064561 | T | C | 88 | a0001c0001t0001g0046 a0002c0002t0002g0002 a0002c0002t0002g0006 others(85): Show |
156 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(153): Show |
intron_variant | MODIFIER | c.23-925A>G | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 1/6 | chr1 | 16064561 | |||||||
| chr1:16064623 | G | A | 11 | a0001c0001t0001g0046 a0002c0002t0002g0013 a0002c0002t0002g0117 others(8): Show |
17 | HG01099.hp2 HG01175.hp2 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.23-987C>T | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 1/6 | chr1 | 16064623 | |||||||
| chr1:16064625 | C | A | 4 | a0003c0003t0008g0051 a0003c0003t0008g0052 a0003c0003t0008g0163 others(1): Show |
6 | HG00323.hp2 HG01167.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.23-989G>T | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 1/6 | chr1 | 16064625 | |||||||
| chr1:16064626 | C | T | 1 | a0001c0001t0001g0121 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.23-990G>A | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 1/6 | chr1 | 16064626 | |||||||
| chr1:16064627 | G | A | 2 | a0001c0001t0001g0067 a0002c0002t0002g0142 |
2 | HG03486.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.23-991C>T | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 1/6 | chr1 | 16064627 | |||||||
| chr1:16064722 | C | T | 8 | a0003c0003t0008g0051 a0003c0003t0008g0052 a0003c0003t0008g0163 others(5): Show |
10 | HG00323.hp2 HG01167.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.23-1086G>A | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 1/6 | chr1 | 16064722 | |||||||
| chr1:16064782 | C | T | 1 | a0001c0001t0001g0073 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.23-1146G>A | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 1/6 | chr1 | 16064782 | |||||||
| chr1:16064832 | A | C | 12 | a0003c0003t0008g0051 a0003c0003t0008g0052 a0003c0003t0008g0163 others(9): Show |
18 | HG00323.hp2 HG01167.hp1 HG01169.hp2 others(15): Show |
intron_variant | MODIFIER | c.23-1196T>G | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 1/6 | chr1 | 16064832 | |||||||
| chr1:16064833 | A | C | 12 | a0003c0003t0008g0051 a0003c0003t0008g0052 a0003c0003t0008g0163 others(9): Show |
18 | HG00323.hp2 HG01167.hp1 HG01169.hp2 others(15): Show |
intron_variant | MODIFIER | c.23-1197T>G | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 1/6 | chr1 | 16064833 | |||||||
| chr1:16064995 | G | A | 1 | a0003c0003t0003g0115 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.23-1359C>T | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 1/6 | chr1 | 16064995 | |||||||
| chr1:16065073 | G | A | 8 | a0003c0003t0008g0051 a0003c0003t0008g0052 a0003c0003t0008g0163 others(5): Show |
10 | HG00323.hp2 HG01167.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.23-1437C>T | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 1/6 | chr1 | 16065073 | |||||||
| chr1:16065122 | C | A | 13 | a0001c0016t0029g0150 a0003c0003t0007g0024 a0003c0003t0007g0050 others(10): Show |
29 | HG00438.hp2 HG01106.hp2 HG01256.hp1 others(26): Show |
intron_variant | MODIFIER | c.23-1486G>T | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 1/6 | chr1 | 16065122 | |||||||
| chr1:16065162 | C | T | 9 | a0003c0003t0008g0051 a0003c0003t0008g0052 a0003c0003t0008g0163 others(6): Show |
12 | HG00323.hp2 HG01167.hp1 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.23-1526G>A | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 1/6 | chr1 | 16065162 | |||||||
| chr1:16065208 | TC | T | 21 | a0001c0001t0001g0046 a0002c0002t0002g0006 a0002c0002t0002g0013 others(18): Show |
38 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(35): Show |
intron_variant | MODIFIER | c.23-1573delG | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 1/6 | chr1 | 16065208 | |||||||
| chr1:16065235 | C | A | 1 | a0006c0006t0012g0058 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.23-1599G>T | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 1/6 | chr1 | 16065235 | |||||||
| chr1:16065256 | G | A | 2 | a0006c0006t0027g0149 a0006c0006t0032g0164 |
2 | HG03453.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.23-1620C>T | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 1/6 | chr1 | 16065256 | |||||||
| chr1:16065264 | T | C | 1 | a0001c0001t0006g0182 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.23-1628A>G | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 1/6 | chr1 | 16065264 | |||||||
| chr1:16065296 | C | T | 5 | a0001c0001t0001g0009 a0001c0001t0001g0029 a0001c0001t0001g0064 others(2): Show |
12 | HG00408.hp2 HG02056.hp2 NA18939.hp1 others(9): Show |
intron_variant | MODIFIER | c.23-1660G>A | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 1/6 | chr1 | 16065296 | |||||||
| chr1:16065342 | G | A | 1 | a0006c0006t0015g0026 | 2 | HG02965.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.23-1706C>T | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 1/6 | chr1 | 16065342 | |||||||
| chr1:16065455 | T | C | 1 | a0004c0004t0004g0100 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.23-1819A>G | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 1/6 | chr1 | 16065455 | |||||||
| chr1:16065480 | T | C | 1 | a0002c0002t0002g0143 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.23-1844A>G | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 1/6 | chr1 | 16065480 | |||||||
| chr1:16065583 | C | T | 11 | a0001c0001t0001g0046 a0002c0002t0002g0013 a0002c0002t0002g0117 others(8): Show |
17 | HG01099.hp2 HG01175.hp2 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.23-1947G>A | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 1/6 | chr1 | 16065583 | |||||||
| chr1:16065663 | T | C | 2 | a0006c0006t0012g0058 a0010c0011t0034g0161 |
2 | HG02572.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.23-2027A>G | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 1/6 | chr1 | 16065663 | |||||||
| chr1:16065694 | C | T | 1 | a0001c0001t0001g0008 | 7 | NA18951.hp2 NA18954.hp2 NA18969.hp2 others(4): Show |
intron_variant | MODIFIER | c.23-2058G>A | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 1/6 | chr1 | 16065694 | |||||||
| chr1:16065885 | G | C | 1 | a0001c0001t0001g0067 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.23-2249C>G | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 1/6 | chr1 | 16065885 | |||||||
| chr1:16065901 | C | CTTTTCT | 2 | a0002c0002t0011g0053 a0002c0002t0033g0165 |
3 | HG02647.hp2 HG02922.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.23-2271_23-2266dup others(6): Show |
FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 1/6 | chr1 | 16065901 | |||||||
| chr1:16065906 | C | CTTTTTCT | 36 | a0003c0003t0003g0005 a0003c0003t0003g0012 a0003c0003t0003g0015 others(33): Show |
62 | HG00639.hp1 HG00738.hp2 HG01069.hp2 others(59): Show |
intron_variant | MODIFIER | c.23-2271_23-2270ins others(7): Show |
FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 1/6 | chr1 | 16065906 | |||||||
| chr1:16065906 | C | CTTTTTCT others(1): Show |
7 | a0003c0003t0008g0051 a0003c0003t0008g0052 a0003c0003t0008g0163 others(4): Show |
9 | HG00323.hp2 HG01167.hp1 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.23-2271_23-2270ins others(8): Show |
FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 1/6 | chr1 | 16065906 | |||||||
| chr1:16065992 | C | T | 44 | a0002c0002t0011g0053 a0002c0002t0033g0165 a0003c0003t0003g0005 others(41): Show |
73 | HG00323.hp2 HG00639.hp1 HG00738.hp2 others(70): Show |
intron_variant | MODIFIER | c.23-2356G>A | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 1/6 | chr1 | 16065992 | |||||||
| chr1:16066013 | C | T | 3 | a0005c0005t0010g0016 a0005c0005t0010g0056 a0005c0005t0010g0057 |
6 | HG02280.hp1 HG02451.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.23-2377G>A | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 1/6 | chr1 | 16066013 | |||||||
| chr1:16066178 | C | T | 1 | a0001c0001t0001g0071 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.23-2542G>A | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 1/6 | chr1 | 16066178 | |||||||
| chr1:16066227 | T | A | 1 | a0013c0020t0003g0116 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.23-2591A>T | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 1/6 | chr1 | 16066227 | |||||||
| chr1:16066406 | G | A | 3 | a0006c0006t0012g0044 a0006c0006t0027g0149 a0006c0006t0032g0164 |
4 | HG01167.hp2 HG02922.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.23-2770C>T | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 1/6 | chr1 | 16066406 | |||||||
| chr1:16066862 | T | G | 68 | a0002c0002t0002g0002 a0002c0002t0002g0018 a0002c0002t0002g0043 others(65): Show |
120 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(117): Show |
intron_variant | MODIFIER | c.23-3226A>C | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 1/6 | chr1 | 16066862 | |||||||
| chr1:16066898 | T | A | 45 | a0002c0002t0011g0053 a0002c0002t0033g0165 a0003c0003t0003g0005 others(42): Show |
74 | HG00323.hp2 HG00639.hp1 HG00738.hp2 others(71): Show |
intron_variant | MODIFIER | c.23-3262A>T | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 1/6 | chr1 | 16066898 | |||||||
| chr1:16067104 | G | A | 1 | a0002c0002t0033g0165 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.23-3468C>T | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 1/6 | chr1 | 16067104 | |||||||
| chr1:16067316 | T | C | 45 | a0002c0002t0011g0053 a0002c0002t0033g0165 a0003c0003t0003g0005 others(42): Show |
74 | HG00323.hp2 HG00639.hp1 HG00738.hp2 others(71): Show |
intron_variant | MODIFIER | c.23-3680A>G | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 1/6 | chr1 | 16067316 | |||||||
| chr1:16067324 | C | T | 7 | a0001c0001t0001g0003 a0001c0001t0001g0028 a0001c0001t0001g0062 others(4): Show |
20 | HG00423.hp2 HG01358.hp2 HG01928.hp2 others(17): Show |
intron_variant | MODIFIER | c.23-3688G>A | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 1/6 | chr1 | 16067324 | |||||||
| chr1:16067345 | C | T | 1 | a0001c0001t0001g0118 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.23-3709G>A | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 1/6 | chr1 | 16067345 | |||||||
| chr1:16067390 | C | T | 1 | a0006c0006t0016g0025 | 2 | HG02486.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.23-3754G>A | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 1/6 | chr1 | 16067390 | |||||||
| chr1:16067396 | C | G | 2 | a0002c0002t0011g0053 a0002c0002t0033g0165 |
3 | HG02647.hp2 HG02922.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.23-3760G>C | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 1/6 | chr1 | 16067396 | |||||||
| chr1:16067457 | G | C | 44 | a0002c0002t0011g0053 a0002c0002t0033g0165 a0003c0003t0003g0005 others(41): Show |
73 | HG00323.hp2 HG00639.hp1 HG00738.hp2 others(70): Show |
intron_variant | MODIFIER | c.23-3821C>G | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 1/6 | chr1 | 16067457 | |||||||
| chr1:16067556 | T | G | 1 | a0012c0022t0025g0139 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.23-3920A>C | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 1/6 | chr1 | 16067556 | |||||||
| chr1:16067557 | G | A | 1 | a0002c0002t0014g0176 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.23-3921C>T | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 1/6 | chr1 | 16067557 | |||||||
| chr1:16067587 | G | A | 1 | a0006c0006t0015g0026 | 2 | HG02965.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.23-3951C>T | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 1/6 | chr1 | 16067587 | |||||||
| chr1:16067827 | G | A | 1 | a0003c0018t0007g0155 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.23-4191C>T | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 1/6 | chr1 | 16067827 | |||||||
| chr1:16067893 | C | A | 45 | a0002c0002t0011g0053 a0002c0002t0033g0165 a0003c0003t0003g0005 others(42): Show |
74 | HG00323.hp2 HG00639.hp1 HG00738.hp2 others(71): Show |
intron_variant | MODIFIER | c.23-4257G>T | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 1/6 | chr1 | 16067893 | |||||||
| chr1:16067946 | G | A | 5 | a0003c0013t0035g0171 a0005c0005t0011g0172 a0005c0005t0018g0157 others(2): Show |
5 | HG01243.hp2 HG02572.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.23-4310C>T | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 1/6 | chr1 | 16067946 | |||||||
| chr1:16068047 | C | T | 1 | a0005c0005t0011g0172 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.23-4411G>A | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 1/6 | chr1 | 16068047 | |||||||
| chr1:16068087 | C | T | 3 | a0001c0001t0001g0020 a0001c0001t0001g0065 a0001c0001t0001g0066 |
5 | HG00423.hp1 HG02074.hp1 HG02129.hp1 others(2): Show |
intron_variant | MODIFIER | c.23-4451G>A | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 1/6 | chr1 | 16068087 | |||||||
| chr1:16068364 | G | A | 11 | a0003c0003t0008g0051 a0003c0003t0008g0052 a0003c0003t0008g0163 others(8): Show |
16 | HG00323.hp2 HG01167.hp1 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.23-4728C>T | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 1/6 | chr1 | 16068364 | |||||||
| chr1:16068393 | C | T | 1 | a0005c0005t0031g0158 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.23-4757G>A | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 1/6 | chr1 | 16068393 | |||||||
| chr1:16068533 | C | T | 2 | a0002c0002t0002g0006 a0002c0002t0002g0027 |
11 | HG01070.hp1 HG01071.hp2 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.22+4888G>A | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 1/6 | chr1 | 16068533 | |||||||
| chr1:16068534 | G | T | 65 | a0002c0002t0002g0002 a0002c0002t0002g0018 a0002c0002t0002g0043 others(62): Show |
117 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(114): Show |
intron_variant | MODIFIER | c.22+4887C>A | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 1/6 | chr1 | 16068534 | |||||||
| chr1:16068652 | G | A | 43 | a0002c0002t0002g0135 a0002c0002t0011g0053 a0003c0003t0003g0005 others(40): Show |
72 | HG00323.hp2 HG00639.hp1 HG00738.hp2 others(69): Show |
intron_variant | MODIFIER | c.22+4769C>T | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 1/6 | chr1 | 16068652 | |||||||
| chr1:16068711 | T | C | 3 | a0005c0005t0010g0016 a0005c0005t0010g0056 a0005c0005t0010g0057 |
6 | HG02280.hp1 HG02451.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.22+4710A>G | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 1/6 | chr1 | 16068711 | |||||||
| chr1:16068712 | C | T | 3 | a0005c0005t0010g0016 a0005c0005t0010g0056 a0005c0005t0010g0057 |
6 | HG02280.hp1 HG02451.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.22+4709G>A | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 1/6 | chr1 | 16068712 | |||||||
| chr1:16068718 | G | A | 1 | a0001c0001t0001g0123 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.22+4703C>T | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 1/6 | chr1 | 16068718 | |||||||
| chr1:16068855 | C | G | 1 | a0003c0013t0035g0171 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.22+4566G>C | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 1/6 | chr1 | 16068855 | |||||||
| chr1:16068867 | C | T | 1 | a0006c0006t0016g0025 | 2 | HG02486.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.22+4554G>A | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 1/6 | chr1 | 16068867 | |||||||
| chr1:16068934 | G | A | 1 | a0002c0002t0011g0053 | 2 | HG02647.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.22+4487C>T | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 1/6 | chr1 | 16068934 | |||||||
| chr1:16068967 | C | T | 4 | a0001c0001t0001g0020 a0001c0001t0001g0065 a0001c0001t0001g0066 others(1): Show |
6 | HG00423.hp1 HG02074.hp1 HG02129.hp1 others(3): Show |
intron_variant | MODIFIER | c.22+4454G>A | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 1/6 | chr1 | 16068967 | |||||||
| chr1:16068992 | C | G | 3 | a0006c0006t0012g0044 a0006c0006t0027g0149 a0006c0006t0032g0164 |
4 | HG01167.hp2 HG02922.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.22+4429G>C | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 1/6 | chr1 | 16068992 | |||||||
| chr1:16068995 | A | G | 9 | a0003c0013t0035g0171 a0006c0006t0012g0044 a0006c0006t0012g0058 others(6): Show |
11 | HG00735.hp2 HG01167.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.22+4426T>C | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 1/6 | chr1 | 16068995 | |||||||
| chr1:16069095 | A | G | 63 | a0001c0001t0001g0046 a0001c0001t0024g0134 a0001c0016t0029g0150 others(60): Show |
120 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(117): Show |
intron_variant | MODIFIER | c.22+4326T>C | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 1/6 | chr1 | 16069095 | |||||||
| chr1:16069108 | G | T | 1 | a0001c0001t0001g0064 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.22+4313C>A | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 1/6 | chr1 | 16069108 | |||||||
| chr1:16069274 | C | T | 1 | a0005c0005t0018g0157 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.22+4147G>A | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 1/6 | chr1 | 16069274 | |||||||
| chr1:16069283 | C | G | 1 | a0002c0002t0014g0173 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.22+4138G>C | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 1/6 | chr1 | 16069283 | |||||||
| chr1:16069454 | G | A | 3 | a0008c0010t0008g0168 a0008c0010t0008g0169 a0008c0010t0008g0170 |
3 | HG00642.hp1 HG02809.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.22+3967C>T | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 1/6 | chr1 | 16069454 | |||||||
| chr1:16069620 | G | T | 4 | a0003c0003t0008g0051 a0005c0005t0010g0016 a0005c0005t0010g0056 others(1): Show |
8 | HG01167.hp1 HG01169.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.22+3801C>A | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 1/6 | chr1 | 16069620 | |||||||
| chr1:16069751 | C | A | 1 | a0006c0006t0012g0044 | 2 | HG01167.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.22+3670G>T | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 1/6 | chr1 | 16069751 | |||||||
| chr1:16069823 | G | A | 18 | a0001c0001t0024g0134 a0002c0002t0002g0002 a0002c0002t0002g0018 others(15): Show |
39 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(36): Show |
intron_variant | MODIFIER | c.22+3598C>T | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 1/6 | chr1 | 16069823 | |||||||
| chr1:16069846 | C | T | 3 | a0005c0005t0010g0016 a0005c0005t0010g0056 a0005c0005t0010g0057 |
6 | HG02280.hp1 HG02451.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.22+3575G>A | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 1/6 | chr1 | 16069846 | |||||||
| chr1:16070051 | T | C | 1 | a0002c0002t0002g0006 | 9 | HG01070.hp1 HG01071.hp2 HG01109.hp2 others(6): Show |
intron_variant | MODIFIER | c.22+3370A>G | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 1/6 | chr1 | 16070051 | |||||||
| chr1:16070103 | A | G | 2 | a0001c0001t0001g0062 a0018c0015t0001g0063 |
2 | NA18999.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.22+3318T>C | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 1/6 | chr1 | 16070103 | |||||||
| chr1:16070123 | T | C | 5 | a0003c0013t0035g0171 a0005c0005t0011g0172 a0005c0005t0018g0157 others(2): Show |
5 | HG01243.hp2 HG02572.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.22+3298A>G | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 1/6 | chr1 | 16070123 | |||||||
| chr1:16070130 | G | C | 2 | a0006c0006t0015g0026 a0006c0006t0016g0025 |
4 | HG02486.hp2 HG02965.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.22+3291C>G | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 1/6 | chr1 | 16070130 | |||||||
| chr1:16070203 | A | G | 45 | a0001c0001t0001g0046 a0001c0016t0029g0150 a0002c0002t0002g0006 others(42): Show |
82 | HG00323.hp2 HG00438.hp2 HG00735.hp2 others(79): Show |
intron_variant | MODIFIER | c.22+3218T>C | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 1/6 | chr1 | 16070203 | |||||||
| chr1:16070311 | T | C | 40 | a0001c0001t0001g0046 a0001c0016t0029g0150 a0002c0002t0002g0006 others(37): Show |
77 | HG00323.hp2 HG00438.hp2 HG00735.hp2 others(74): Show |
intron_variant | MODIFIER | c.22+3110A>G | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 1/6 | chr1 | 16070311 | |||||||
| chr1:16070401 | C | T | 3 | a0002c0002t0002g0137 a0002c0002t0002g0144 a0002c0002t0019g0136 |
3 | HG02258.hp2 HG02486.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.22+3020G>A | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 1/6 | chr1 | 16070401 | |||||||
| chr1:16070407 | CT | C | 3 | a0003c0003t0008g0051 a0003c0003t0008g0052 a0003c0003t0008g0163 |
5 | HG00323.hp2 HG01167.hp1 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.22+3013delA | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 1/6 | chr1 | 16070407 | |||||||
| chr1:16070689 | G | A | 4 | a0001c0001t0001g0118 a0001c0001t0001g0120 a0004c0007t0004g0041 others(1): Show |
5 | HG00280.hp1 HG00673.hp2 NA18963.hp1 others(2): Show |
intron_variant | MODIFIER | c.22+2732C>T | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 1/6 | chr1 | 16070689 | |||||||
| chr1:16070853 | A | G | 2 | a0003c0003t0003g0059 a0003c0003t0003g0061 |
2 | HG02622.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.22+2568T>C | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 1/6 | chr1 | 16070853 | |||||||
| chr1:16070875 | C | T | 1 | a0001c0001t0006g0177 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.22+2546G>A | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 1/6 | chr1 | 16070875 | |||||||
| chr1:16070984 | G | T | 1 | a0005c0005t0011g0166 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.22+2437C>A | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 1/6 | chr1 | 16070984 | |||||||
| chr1:16070985 | C | T | 1 | a0005c0005t0011g0166 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.22+2436G>A | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 1/6 | chr1 | 16070985 | |||||||
| chr1:16071079 | C | T | 1 | a0001c0001t0001g0060 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.22+2342G>A | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 1/6 | chr1 | 16071079 | |||||||
| chr1:16071238 | AG | A | 33 | a0001c0001t0001g0046 a0001c0016t0029g0150 a0002c0002t0002g0006 others(30): Show |
67 | HG00438.hp2 HG00735.hp2 HG01070.hp1 others(64): Show |
intron_variant | MODIFIER | c.22+2182delC | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 1/6 | chr1 | 16071238 | |||||||
| chr1:16071241 | G | C | 1 | a0001c0001t0001g0121 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.22+2180C>G | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 1/6 | chr1 | 16071241 | |||||||
| chr1:16071356 | A | G | 1 | a0006c0006t0012g0044 | 2 | HG01167.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.22+2065T>C | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 1/6 | chr1 | 16071356 | |||||||
| chr1:16071375 | T | C | 33 | a0001c0001t0001g0046 a0001c0016t0029g0150 a0002c0002t0002g0006 others(30): Show |
67 | HG00438.hp2 HG00735.hp2 HG01070.hp1 others(64): Show |
intron_variant | MODIFIER | c.22+2046A>G | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 1/6 | chr1 | 16071375 | |||||||
| chr1:16071475 | A | G | 23 | a0002c0002t0011g0053 a0002c0002t0033g0165 a0003c0003t0008g0051 others(20): Show |
31 | HG00323.hp2 HG00642.hp1 HG01167.hp1 others(28): Show |
intron_variant | MODIFIER | c.22+1946T>C | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 1/6 | chr1 | 16071475 | |||||||
| chr1:16071512 | A | G | 1 | a0003c0003t0003g0059 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.22+1909T>C | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 1/6 | chr1 | 16071512 | |||||||
| chr1:16071820 | G | A | 1 | a0005c0005t0010g0057 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.22+1601C>T | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 1/6 | chr1 | 16071820 | |||||||
| chr1:16071880 | T | C | 73 | a0001c0001t0001g0046 a0001c0001t0001g0123 a0001c0001t0024g0134 others(70): Show |
135 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(132): Show |
intron_variant | MODIFIER | c.22+1541A>G | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 1/6 | chr1 | 16071880 | |||||||
| chr1:16071951 | T | C | 3 | a0002c0002t0011g0053 a0002c0002t0033g0165 a0006c0006t0032g0164 |
4 | HG02647.hp2 HG02922.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.22+1470A>G | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 1/6 | chr1 | 16071951 | |||||||
| chr1:16072088 | C | T | 1 | a0010c0011t0034g0161 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.22+1333G>A | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 1/6 | chr1 | 16072088 | |||||||
| chr1:16072101 | G | C | 1 | a0010c0011t0034g0161 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.22+1320C>G | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 1/6 | chr1 | 16072101 | |||||||
| chr1:16072231 | T | A | 1 | a0002c0002t0002g0144 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.22+1190A>T | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 1/6 | chr1 | 16072231 | |||||||
| chr1:16072260 | G | A | 1 | a0003c0003t0007g0156 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.22+1161C>T | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 1/6 | chr1 | 16072260 | |||||||
| chr1:16072350 | G | A | 1 | a0010c0011t0034g0161 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.22+1071C>T | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 1/6 | chr1 | 16072350 | |||||||
| chr1:16072487 | C | T | 1 | a0006c0006t0032g0164 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.22+934G>A | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 1/6 | chr1 | 16072487 | |||||||
| chr1:16072624 | T | C | 16 | a0001c0001t0011g0162 a0002c0002t0011g0053 a0002c0002t0033g0165 others(13): Show |
22 | HG00323.hp2 HG01167.hp1 HG01169.hp2 others(19): Show |
intron_variant | MODIFIER | c.22+797A>G | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 1/6 | chr1 | 16072624 | |||||||
| chr1:16072965 | A | G | 1 | a0006c0006t0008g0160 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.22+456T>C | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 1/6 | chr1 | 16072965 | |||||||
| chr1:16073162 | G | C | 3 | a0002c0002t0011g0053 a0002c0002t0033g0165 a0006c0006t0032g0164 |
4 | HG02647.hp2 HG02922.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.22+259C>G | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 1/6 | chr1 | 16073162 | |||||||
| chr1:16073169 | G | T | 4 | a0003c0013t0035g0171 a0005c0005t0018g0157 a0005c0005t0018g0159 others(1): Show |
4 | HG01243.hp2 HG02572.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.22+252C>A | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 1/6 | chr1 | 16073169 | |||||||
| chr1:16073292 | G | A | 5 | a0005c0005t0011g0166 a0005c0005t0011g0167 a0008c0010t0008g0168 others(2): Show |
5 | HG00642.hp1 HG02809.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.22+129C>T | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 1/6 | chr1 | 16073292 | |||||||
| chr1:16073345 | C | T | 1 | a0006c0006t0012g0058 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.22+76G>A | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 1/6 | chr1 | 16073345 | |||||||
| chr1:16073355 | G | A | 5 | a0003c0013t0035g0171 a0005c0005t0011g0172 a0005c0005t0018g0157 others(2): Show |
5 | HG01243.hp2 HG02572.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.22+66C>T | FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 1/6 | chr1 | 16073355 |