Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 84140 |
| ensemblid | ENSG00000170264.13 |
| hgncid | 25808 |
| symbol | FAM161A |
| name | FAM161 centrosomal protein A |
| refseq_nuc | NM_001201543.2 |
| refseq_prot | NP_001188472.1 |
| ensembl_nuc | ENST00000404929.6 |
| ensembl_prot | ENSP00000385158.1 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 61824848 |
| end | 61854060 |
| strand | - |
| ver | v1.2 |
| region | chr2:61824848-61854060 |
| region5000 | chr2:61819848-61859060 |
| regionname0 | FAM161A_chr2_61824848_61854060 |
| regionname5000 | FAM161A_chr2_61819848_61859060 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 716 | 275 | 64 | 48 | 125 | 12 | 24 | 92 | FAM161A_chr2_61819848_61859060 | FAM161A | MATSH others(711): Show |
chr2 | 61819848 | 61859060 |
| a0002 | 0/0 | 716 | 68 | 8 | 9 | 38 | 4 | 9 | 33 | FAM161A_chr2_61819848_61859060 | FAM161A | MATSH others(711): Show |
chr2 | 61819848 | 61859060 |
| a0003 | 0/0 | 716 | 37 | 4 | 12 | 15 | 2 | 4 | 11 | FAM161A_chr2_61819848_61859060 | FAM161A | MATSH others(711): Show |
chr2 | 61819848 | 61859060 |
| a0004 | 0/0 | 716 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | MATSH others(711): Show |
chr2 | 61819848 | 61859060 |
| a0005 | 0/0 | 716 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | MATSH others(711): Show |
chr2 | 61819848 | 61859060 |
| a0006 | 0/0 | 716 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | MATSH others(711): Show |
chr2 | 61819848 | 61859060 |
| a0007 | 0/0 | 716 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | MATSH others(711): Show |
chr2 | 61819848 | 61859060 |
| a0008 | 0/0 | 716 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | MATSH others(711): Show |
chr2 | 61819848 | 61859060 |
| a0009 | 0/0 | 716 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | MATSH others(711): Show |
chr2 | 61819848 | 61859060 |
| a0010 | 0/0 | 716 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | MATSH others(711): Show |
chr2 | 61819848 | 61859060 |
| a0011 | 0/0 | 716 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | MATSH others(711): Show |
chr2 | 61819848 | 61859060 |
| a0012 | 0/0 | 716 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | MATSH others(711): Show |
chr2 | 61819848 | 61859060 |
| a0013 | 0/0 | 716 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | MATSH others(711): Show |
chr2 | 61819848 | 61859060 |
| a0014 | 0/0 | 716 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FAM161A_chr2_61819848_61859060 | FAM161A | MATSH others(711): Show |
chr2 | 61819848 | 61859060 |
| a0015 | 0/0 | 716 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FAM161A_chr2_61819848_61859060 | FAM161A | MATSH others(711): Show |
chr2 | 61819848 | 61859060 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 2148 | 215 | 61 | 30 | 93 | 9 | 21 | FAM161A_chr2_61819848_61859060 | FAM161A | ATGGC others(2143): Show |
chr2 | 61819848 | 61859060 | ||
| a0001c0003 | 0/0 | 2148 | 54 | 1 | 16 | 32 | 2 | 3 | FAM161A_chr2_61819848_61859060 | FAM161A | ATGGC others(2143): Show |
chr2 | 61819848 | 61859060 | ||
| a0001c0006 | 1/0 | 2148 | 4 | 0 | 2 | 0 | 1 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | ATGGC others(2143): Show |
chr2 | 61819848 | 61859060 | ||
| a0001c0013 | 0/0 | 2148 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | ATGGC others(2143): Show |
chr2 | 61819848 | 61859060 | ||
| a0001c0019 | 0/0 | 2148 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | ATGGC others(2143): Show |
chr2 | 61819848 | 61859060 | ||
| a0002c0002 | 0/0 | 2148 | 67 | 8 | 9 | 38 | 4 | 8 | FAM161A_chr2_61819848_61859060 | FAM161A | ATGGC others(2143): Show |
chr2 | 61819848 | 61859060 | ||
| a0002c0020 | 0/0 | 2148 | 1 | 0 | 0 | 0 | 0 | 1 | FAM161A_chr2_61819848_61859060 | FAM161A | ATGGC others(2143): Show |
chr2 | 61819848 | 61859060 | ||
| a0003c0004 | 0/0 | 2148 | 37 | 4 | 12 | 15 | 2 | 4 | FAM161A_chr2_61819848_61859060 | FAM161A | ATGGC others(2143): Show |
chr2 | 61819848 | 61859060 | ||
| a0004c0005 | 0/0 | 2148 | 6 | 6 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | ATGGC others(2143): Show |
chr2 | 61819848 | 61859060 | ||
| a0005c0007 | 0/0 | 2148 | 2 | 2 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | ATGGC others(2143): Show |
chr2 | 61819848 | 61859060 | ||
| a0005c0010 | 0/0 | 2148 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | ATGGC others(2143): Show |
chr2 | 61819848 | 61859060 | ||
| a0006c0008 | 0/0 | 2148 | 2 | 0 | 0 | 0 | 0 | 2 | FAM161A_chr2_61819848_61859060 | FAM161A | ATGGC others(2143): Show |
chr2 | 61819848 | 61859060 | ||
| a0007c0016 | 0/0 | 2148 | 1 | 0 | 1 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | ATGGC others(2143): Show |
chr2 | 61819848 | 61859060 | ||
| a0008c0014 | 0/0 | 2148 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | ATGGC others(2143): Show |
chr2 | 61819848 | 61859060 | ||
| a0009c0011 | 0/0 | 2148 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | ATGGC others(2143): Show |
chr2 | 61819848 | 61859060 | ||
| a0010c0021 | 0/0 | 2148 | 1 | 0 | 0 | 0 | 0 | 1 | FAM161A_chr2_61819848_61859060 | FAM161A | ATGGC others(2143): Show |
chr2 | 61819848 | 61859060 | ||
| a0011c0018 | 0/0 | 2148 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | ATGGC others(2143): Show |
chr2 | 61819848 | 61859060 | ||
| a0012c0012 | 0/0 | 2148 | 1 | 0 | 0 | 0 | 0 | 1 | FAM161A_chr2_61819848_61859060 | FAM161A | ATGGC others(2143): Show |
chr2 | 61819848 | 61859060 | ||
| a0013c0017 | 0/0 | 2148 | 1 | 0 | 0 | 0 | 0 | 1 | FAM161A_chr2_61819848_61859060 | FAM161A | ATGGC others(2143): Show |
chr2 | 61819848 | 61859060 | ||
| a0014c0009 | 0/0 | 2148 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | ATGGC others(2143): Show |
chr2 | 61819848 | 61859060 | ||
| a0015c0015 | 0/0 | 2148 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | ATGGC others(2143): Show |
chr2 | 61819848 | 61859060 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3777 | 119 | 22 | 13 | 79 | 0 | 5 | FAM161A_chr2_61819848_61859060 | FAM161A | AGGCC others(3772): Show |
chr2 | 61819848 | 61859060 |
| a0001c0001t0002 | 0/1 | 3777 | 61 | 31 | 8 | 10 | 1 | 10 | FAM161A_chr2_61819848_61859060 | FAM161A | AGGCC others(3772): Show |
chr2 | 61819848 | 61859060 |
| a0001c0001t0004 | 0/0 | 3774 | 19 | 0 | 9 | 0 | 4 | 6 | FAM161A_chr2_61819848_61859060 | FAM161A | AGGCC others(3769): Show |
chr2 | 61819848 | 61859060 |
| a0001c0001t0006 | 0/0 | 3777 | 2 | 2 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | AGGCC others(3772): Show |
chr2 | 61819848 | 61859060 |
| a0001c0001t0007 | 0/0 | 3777 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | AGGCC others(3772): Show |
chr2 | 61819848 | 61859060 |
| a0001c0001t0008 | 0/0 | 3777 | 2 | 0 | 0 | 0 | 2 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | AGGCC others(3772): Show |
chr2 | 61819848 | 61859060 |
| a0001c0001t0010 | 0/0 | 3777 | 2 | 2 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | AGGGC others(3772): Show |
chr2 | 61819848 | 61859060 |
| a0001c0001t0011 | 0/0 | 3777 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | AGGCC others(3772): Show |
chr2 | 61819848 | 61859060 |
| a0001c0001t0013 | 0/0 | 3777 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | AGGCC others(3772): Show |
chr2 | 61819848 | 61859060 |
| a0001c0001t0016 | 0/0 | 3777 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | AGGCC others(3772): Show |
chr2 | 61819848 | 61859060 |
| a0001c0001t0017 | 0/0 | 3777 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | AGGCC others(3772): Show |
chr2 | 61819848 | 61859060 |
| a0001c0001t0020 | 0/0 | 3777 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | AGGCC others(3772): Show |
chr2 | 61819848 | 61859060 |
| a0001c0001t0021 | 0/0 | 3777 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | AGGCC others(3772): Show |
chr2 | 61819848 | 61859060 |
| a0001c0001t0022 | 0/0 | 3777 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | AGGCC others(3772): Show |
chr2 | 61819848 | 61859060 |
| a0001c0001t0023 | 0/0 | 3777 | 1 | 0 | 0 | 0 | 1 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | AGGCC others(3772): Show |
chr2 | 61819848 | 61859060 |
| a0001c0001t0024 | 0/0 | 3774 | 1 | 0 | 0 | 0 | 1 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | AGGCC others(3769): Show |
chr2 | 61819848 | 61859060 |
| a0001c0003t0001 | 0/0 | 3777 | 53 | 1 | 16 | 32 | 1 | 3 | FAM161A_chr2_61819848_61859060 | FAM161A | AGGCC others(3772): Show |
chr2 | 61819848 | 61859060 |
| a0001c0003t0014 | 0/0 | 3777 | 1 | 0 | 0 | 0 | 1 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | AGGCC others(3772): Show |
chr2 | 61819848 | 61859060 |
| a0001c0006t0002 | 1/0 | 3777 | 4 | 0 | 2 | 0 | 1 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | AGGCC others(3772): Show |
chr2 | 61819848 | 61859060 |
| a0001c0013t0001 | 0/0 | 3777 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | AGGCC others(3772): Show |
chr2 | 61819848 | 61859060 |
| a0001c0019t0007 | 0/0 | 3777 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | AGGCC others(3772): Show |
chr2 | 61819848 | 61859060 |
| a0002c0002t0002 | 0/0 | 3777 | 65 | 6 | 9 | 38 | 4 | 8 | FAM161A_chr2_61819848_61859060 | FAM161A | AGGCC others(3772): Show |
chr2 | 61819848 | 61859060 |
| a0002c0002t0012 | 0/0 | 3777 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | AGGCC others(3772): Show |
chr2 | 61819848 | 61859060 |
| a0002c0002t0019 | 0/0 | 3777 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | AGGCC others(3772): Show |
chr2 | 61819848 | 61859060 |
| a0002c0020t0002 | 0/0 | 3777 | 1 | 0 | 0 | 0 | 0 | 1 | FAM161A_chr2_61819848_61859060 | FAM161A | AGGCC others(3772): Show |
chr2 | 61819848 | 61859060 |
| a0003c0004t0003 | 0/0 | 3776 | 37 | 4 | 12 | 15 | 2 | 4 | FAM161A_chr2_61819848_61859060 | FAM161A | AGGCC others(3771): Show |
chr2 | 61819848 | 61859060 |
| a0004c0005t0002 | 0/0 | 3777 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | AGGCC others(3772): Show |
chr2 | 61819848 | 61859060 |
| a0004c0005t0005 | 0/0 | 3777 | 5 | 5 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | AGGCC others(3772): Show |
chr2 | 61819848 | 61859060 |
| a0005c0007t0009 | 0/0 | 3777 | 2 | 2 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | AGGCC others(3772): Show |
chr2 | 61819848 | 61859060 |
| a0005c0010t0018 | 0/0 | 3777 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | AGGCC others(3772): Show |
chr2 | 61819848 | 61859060 |
| a0006c0008t0002 | 0/0 | 3777 | 2 | 0 | 0 | 0 | 0 | 2 | FAM161A_chr2_61819848_61859060 | FAM161A | AGGCC others(3772): Show |
chr2 | 61819848 | 61859060 |
| a0007c0016t0003 | 0/0 | 3776 | 1 | 0 | 1 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | AGGCC others(3771): Show |
chr2 | 61819848 | 61859060 |
| a0008c0014t0002 | 0/0 | 3777 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | AGGCC others(3772): Show |
chr2 | 61819848 | 61859060 |
| a0009c0011t0002 | 0/0 | 3777 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | AGGCC others(3772): Show |
chr2 | 61819848 | 61859060 |
| a0010c0021t0004 | 0/0 | 3774 | 1 | 0 | 0 | 0 | 0 | 1 | FAM161A_chr2_61819848_61859060 | FAM161A | AGGCC others(3769): Show |
chr2 | 61819848 | 61859060 |
| a0011c0018t0015 | 0/0 | 3777 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | AGGCC others(3772): Show |
chr2 | 61819848 | 61859060 |
| a0012c0012t0002 | 0/0 | 3777 | 1 | 0 | 0 | 0 | 0 | 1 | FAM161A_chr2_61819848_61859060 | FAM161A | AGGCC others(3772): Show |
chr2 | 61819848 | 61859060 |
| a0013c0017t0003 | 0/0 | 3776 | 1 | 0 | 0 | 0 | 0 | 1 | FAM161A_chr2_61819848_61859060 | FAM161A | AGGCC others(3771): Show |
chr2 | 61819848 | 61859060 |
| a0014c0009t0002 | 0/0 | 3777 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | AGGCC others(3772): Show |
chr2 | 61819848 | 61859060 |
| a0015c0015t0001 | 0/0 | 3777 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | AGGCC others(3772): Show |
chr2 | 61819848 | 61859060 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 16 | 0 | 0 | 13 | 0 | 3 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0001g0006 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0001g0008 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0001g0010 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0001g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0001g0050 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0002g0004 | 0/0 | 8 | 2 | 2 | 0 | 0 | 4 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0002g0009 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0002g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0002g0017 | 0/0 | 3 | 0 | 0 | 0 | 1 | 2 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0002g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0002g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0002g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0002g0176 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0002g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0002g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0002g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0002g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0002g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0002g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0002g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0002g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0002g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0002g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0002g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0002g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0002g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0002g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0002g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0002g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0004g0011 | 0/0 | 4 | 0 | 2 | 0 | 2 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0004g0013 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0004g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0004g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0004g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0004g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0004g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0004g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0004g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0004g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0004g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0004g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0004g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0004g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0006g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0006g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0007g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0008g0041 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0010g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0010g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0011g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0013g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0016g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0017g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0020g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0021g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0022g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0023g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0001t0024g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0003t0001g0002 | 0/0 | 16 | 0 | 8 | 8 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0003t0001g0005 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0003t0001g0012 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0003t0001g0029 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0003t0001g0032 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0003t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0003t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0003t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0003t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0003t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0003t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0003t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0003t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0003t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0003t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0003t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0003t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0003t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0003t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0003t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0003t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0003t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0003t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0003t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0003t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0003t0014g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0006t0002g0268 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0006t0002g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0006t0002g0270 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0006t0002g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0013t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0001c0019t0007g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0002c0002t0002g0007 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0002c0002t0002g0018 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0002c0002t0002g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0002c0002t0002g0020 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0002c0002t0002g0021 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0002c0002t0002g0042 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0002c0002t0002g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0002c0002t0002g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0002c0002t0002g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0002c0002t0002g0046 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0002c0002t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0002c0002t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0002c0002t0002g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0002c0002t0002g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0002c0002t0002g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0002c0002t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0002c0002t0002g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0002c0002t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0002c0002t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0002c0002t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0002c0002t0002g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0002c0002t0002g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0002c0002t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0002c0002t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0002c0002t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0002c0002t0002g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0002c0002t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0002c0002t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0002c0002t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0002c0002t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0002c0002t0002g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0002c0002t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0002c0002t0002g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0002c0002t0002g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0002c0002t0002g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0002c0002t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0002c0002t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0002c0002t0002g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0002c0002t0002g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0002c0002t0002g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0002c0002t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0002c0002t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0002c0002t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0002c0002t0002g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0002c0002t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0002c0002t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0002c0002t0012g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0002c0002t0019g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0002c0020t0002g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0003c0004t0003g0003 | 0/0 | 8 | 1 | 2 | 5 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0003c0004t0003g0015 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0003c0004t0003g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0003c0004t0003g0039 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0003c0004t0003g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0003c0004t0003g0047 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0003c0004t0003g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0003c0004t0003g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0003c0004t0003g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0003c0004t0003g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0003c0004t0003g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0003c0004t0003g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0003c0004t0003g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0003c0004t0003g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0003c0004t0003g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0003c0004t0003g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0003c0004t0003g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0003c0004t0003g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0003c0004t0003g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0003c0004t0003g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0003c0004t0003g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0003c0004t0003g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0003c0004t0003g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0003c0004t0003g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0004c0005t0002g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0004c0005t0005g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0004c0005t0005g0049 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0004c0005t0005g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0005c0007t0009g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0005c0007t0009g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0005c0010t0018g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0006c0008t0002g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0006c0008t0002g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0007c0016t0003g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0008c0014t0002g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0009c0011t0002g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0010c0021t0004g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0011c0018t0015g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0012c0012t0002g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0013c0017t0003g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0014c0009t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| a0015c0015t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0002 | t0002 | g0212 | EUR | GBR | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG00099 | hp2 | a0001 | c0001 | t0004 | g0011 | EUR | GBR | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG00140 | hp1 | a0003 | c0004 | t0003 | g0118 | EUR | GBR | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG00140 | hp2 | a0001 | c0001 | t0004 | g0061 | EUR | GBR | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG00280 | hp1 | a0003 | c0004 | t0003 | g0170 | EUR | FIN | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG00280 | hp2 | a0001 | c0006 | t0002 | g0268 | EUR | FIN | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG00323 | hp1 | a0001 | c0001 | t0024 | g0089 | EUR | FIN | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG00323 | hp2 | a0002 | c0002 | t0002 | g0223 | EUR | FIN | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG00408 | hp1 | a0002 | c0002 | t0002 | g0226 | EAS | CHS | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | CHS | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | CHS | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG00423 | hp2 | a0003 | c0004 | t0003 | g0169 | EAS | CHS | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG00438 | hp1 | a0001 | c0003 | t0001 | g0034 | EAS | CHS | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | CHS | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | CHS | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | CHS | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG00558 | hp1 | a0001 | c0003 | t0001 | g0136 | EAS | CHS | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG00597 | hp1 | a0001 | c0001 | t0022 | g0133 | EAS | CHS | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG00597 | hp2 | a0003 | c0004 | t0003 | g0165 | EAS | CHS | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG00621 | hp1 | a0001 | c0003 | t0001 | g0012 | EAS | CHS | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | CHS | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG00639 | hp1 | a0003 | c0004 | t0003 | g0003 | AMR | PUR | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0218 | AMR | PUR | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG00642 | hp1 | a0003 | c0004 | t0003 | g0166 | AMR | PUR | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | PUR | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG00673 | hp1 | a0003 | c0004 | t0003 | g0040 | EAS | CHS | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | CHS | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG00735 | hp2 | a0001 | c0001 | t0004 | g0092 | AMR | PUR | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG00738 | hp1 | a0001 | c0003 | t0001 | g0032 | AMR | PUR | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG00738 | hp2 | a0002 | c0002 | t0002 | g0237 | AMR | PUR | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG00741 | hp1 | a0003 | c0004 | t0003 | g0015 | AMR | PUR | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG00741 | hp2 | a0001 | c0001 | t0004 | g0064 | AMR | PUR | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG01070 | hp1 | a0001 | c0003 | t0001 | g0127 | AMR | PUR | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG01070 | hp2 | a0003 | c0004 | t0003 | g0161 | AMR | PUR | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG01071 | hp1 | a0001 | c0003 | t0001 | g0002 | AMR | PUR | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG01071 | hp2 | a0003 | c0004 | t0003 | g0162 | AMR | PUR | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG01074 | hp1 | a0001 | c0003 | t0001 | g0002 | AMR | PUR | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | PUR | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG01081 | hp1 | a0001 | c0001 | t0004 | g0059 | AMR | PUR | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG01081 | hp2 | a0003 | c0004 | t0003 | g0031 | AMR | PUR | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG01099 | hp1 | a0001 | c0003 | t0001 | g0146 | AMR | PUR | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG01099 | hp2 | a0003 | c0004 | t0003 | g0031 | AMR | PUR | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG01109 | hp2 | a0003 | c0004 | t0003 | g0039 | AMR | PUR | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | PUR | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0199 | AMR | PUR | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG01169 | hp1 | a0002 | c0002 | t0002 | g0203 | AMR | PUR | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0095 | AMR | PUR | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG01175 | hp1 | a0001 | c0003 | t0001 | g0029 | AMR | PUR | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0179 | AMR | PUR | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG01192 | hp1 | a0001 | c0003 | t0001 | g0125 | AMR | PUR | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG01192 | hp2 | a0002 | c0002 | t0002 | g0238 | AMR | PUR | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG01255 | hp1 | a0007 | c0016 | t0003 | g0163 | AMR | CLM | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0220 | AMR | CLM | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG01256 | hp1 | a0002 | c0002 | t0002 | g0021 | AMR | CLM | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG01256 | hp2 | a0002 | c0002 | t0002 | g0018 | AMR | CLM | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG01257 | hp1 | a0001 | c0001 | t0004 | g0011 | AMR | CLM | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0180 | AMR | CLM | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0187 | AMR | CLM | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG01258 | hp2 | a0002 | c0002 | t0002 | g0021 | AMR | CLM | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG01261 | hp1 | a0001 | c0003 | t0001 | g0002 | AMR | CLM | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG01261 | hp2 | a0001 | c0006 | t0002 | g0269 | AMR | CLM | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG01346 | hp1 | a0002 | c0002 | t0002 | g0240 | AMR | CLM | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG01346 | hp2 | a0003 | c0004 | t0003 | g0015 | AMR | CLM | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG01358 | hp1 | a0001 | c0003 | t0001 | g0002 | AMR | CLM | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG01358 | hp2 | a0001 | c0001 | t0004 | g0013 | AMR | CLM | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG01361 | hp1 | a0003 | c0004 | t0003 | g0109 | AMR | CLM | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG01361 | hp2 | a0001 | c0001 | t0004 | g0082 | AMR | CLM | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG01433 | hp1 | a0001 | c0001 | t0004 | g0062 | AMR | CLM | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG01433 | hp2 | a0001 | c0001 | t0004 | g0013 | AMR | CLM | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG01496 | hp2 | a0001 | c0001 | t0004 | g0011 | AMR | CLM | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG01515 | hp1 | a0001 | c0001 | t0008 | g0041 | EUR | IBS | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG01515 | hp2 | a0001 | c0003 | t0001 | g0243 | EUR | IBS | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG01516 | hp1 | a0001 | c0001 | t0004 | g0011 | EUR | IBS | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG01516 | hp2 | a0002 | c0002 | t0002 | g0018 | EUR | IBS | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG01517 | hp1 | a0001 | c0001 | t0008 | g0041 | EUR | IBS | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG01517 | hp2 | a0002 | c0002 | t0002 | g0018 | EUR | IBS | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | ACB | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | ACB | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | ACB | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0186 | AFR | ACB | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG01928 | hp2 | a0001 | c0003 | t0001 | g0002 | AMR | PEL | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG01934 | hp1 | a0001 | c0003 | t0001 | g0129 | AMR | PEL | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG01943 | hp1 | a0002 | c0002 | t0002 | g0020 | AMR | PEL | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG01943 | hp2 | a0001 | c0006 | t0002 | g0271 | AMR | PEL | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG01978 | hp2 | a0001 | c0003 | t0001 | g0002 | AMR | PEL | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG01981 | hp1 | a0001 | c0003 | t0001 | g0012 | AMR | PEL | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG01981 | hp2 | a0003 | c0004 | t0003 | g0246 | AMR | PEL | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | PEL | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0051 | AMR | PEL | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG02015 | hp1 | a0001 | c0003 | t0001 | g0124 | EAS | KHV | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG02015 | hp2 | a0001 | c0001 | t0013 | g0148 | EAS | KHV | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG02027 | hp2 | a0001 | c0003 | t0001 | g0005 | EAS | KHV | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | KHV | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG02040 | hp2 | a0001 | c0003 | t0001 | g0005 | EAS | KHV | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0177 | AFR | ACB | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG02056 | hp1 | a0002 | c0002 | t0002 | g0044 | EAS | KHV | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | KHV | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG02074 | hp1 | a0001 | c0003 | t0001 | g0138 | EAS | KHV | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG02074 | hp2 | a0002 | c0002 | t0002 | g0235 | EAS | KHV | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0134 | EAS | KHV | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG02129 | hp1 | a0001 | c0003 | t0001 | g0002 | EAS | KHV | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG02132 | hp1 | a0001 | c0003 | t0001 | g0158 | EAS | KHV | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG02132 | hp2 | a0003 | c0004 | t0003 | g0100 | EAS | KHV | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG02145 | hp1 | a0002 | c0002 | t0012 | g0115 | AFR | ACB | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | CDX | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | CDX | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG02258 | hp1 | a0003 | c0004 | t0003 | g0003 | AFR | ACB | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG02258 | hp2 | a0001 | c0001 | t0006 | g0142 | AFR | ACB | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG02273 | hp1 | a0001 | c0003 | t0001 | g0002 | AMR | PEL | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PEL | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG02280 | hp1 | a0004 | c0005 | t0005 | g0049 | AFR | ACB | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0259 | AFR | ACB | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG02300 | hp1 | a0001 | c0003 | t0001 | g0002 | AMR | PEL | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG02300 | hp2 | a0002 | c0002 | t0002 | g0042 | AMR | PEL | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG02451 | hp1 | a0004 | c0005 | t0002 | g0249 | AFR | ACB | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0248 | AFR | ACB | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG02523 | hp1 | a0002 | c0002 | t0002 | g0241 | EAS | KHV | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | KHV | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG02572 | hp1 | a0005 | c0007 | t0009 | g0264 | AFR | GWD | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG02572 | hp2 | a0008 | c0014 | t0002 | g0189 | AFR | GWD | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG02602 | hp1 | a0003 | c0004 | t0003 | g0164 | SAS | PJL | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0198 | SAS | PJL | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0182 | AFR | GWD | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG02622 | hp1 | a0005 | c0010 | t0018 | g0262 | AFR | GWD | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0201 | AFR | GWD | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0266 | AFR | GWD | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG02647 | hp1 | a0002 | c0002 | t0002 | g0204 | AFR | GWD | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG02647 | hp2 | a0002 | c0002 | t0002 | g0043 | AFR | GWD | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG02683 | hp1 | a0002 | c0002 | t0002 | g0202 | SAS | PJL | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG02683 | hp2 | a0001 | c0001 | t0004 | g0065 | SAS | PJL | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG02698 | hp1 | a0001 | c0003 | t0001 | g0029 | SAS | PJL | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0004 | SAS | PJL | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG02723 | hp1 | a0002 | c0002 | t0002 | g0208 | AFR | GWD | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG02723 | hp2 | a0002 | c0002 | t0002 | g0043 | AFR | GWD | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0004 | SAS | PJL | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG02738 | hp1 | a0002 | c0002 | t0002 | g0234 | SAS | PJL | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0093 | SAS | PJL | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG02809 | hp1 | a0001 | c0003 | t0001 | g0126 | AFR | GWD | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0016 | AFR | GWD | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG02886 | hp1 | a0001 | c0001 | t0017 | g0117 | AFR | GWD | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG02886 | hp2 | a0001 | c0001 | t0020 | g0191 | AFR | GWD | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | GWD | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0229 | AFR | GWD | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG02896 | hp1 | a0002 | c0002 | t0002 | g0254 | AFR | GWD | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0251 | AFR | GWD | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | GWD | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0206 | AFR | GWD | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG02922 | hp1 | a0001 | c0001 | t0010 | g0273 | AFR | ESN | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0190 | AFR | ESN | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG02965 | hp1 | a0009 | c0011 | t0002 | g0247 | AFR | ESN | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG02965 | hp2 | a0003 | c0004 | t0003 | g0160 | AFR | ESN | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0184 | AFR | ESN | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG02970 | hp2 | a0001 | c0001 | t0010 | g0272 | AFR | ESN | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0205 | AFR | ESN | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0244 | AFR | ESN | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG03017 | hp1 | a0010 | c0021 | t0004 | g0084 | SAS | PJL | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0004 | SAS | PJL | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG03041 | hp1 | a0004 | c0005 | t0005 | g0250 | AFR | GWD | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG03098 | hp1 | a0002 | c0002 | t0002 | g0228 | AFR | MSL | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0260 | AFR | MSL | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG03130 | hp1 | a0001 | c0001 | t0006 | g0140 | AFR | ESN | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG03130 | hp2 | a0005 | c0007 | t0009 | g0263 | AFR | ESN | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0016 | AFR | ESN | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG03195 | hp1 | a0011 | c0018 | t0015 | g0261 | AFR | ESN | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | ESN | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0009 | AFR | MSL | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0009 | AFR | MSL | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG03239 | hp1 | a0003 | c0004 | t0003 | g0039 | SAS | PJL | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG03239 | hp2 | a0001 | c0003 | t0001 | g0242 | SAS | PJL | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG03453 | hp1 | a0004 | c0005 | t0005 | g0049 | AFR | MSL | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG03453 | hp2 | a0001 | c0019 | t0007 | g0143 | AFR | MSL | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG03486 | hp1 | a0001 | c0013 | t0001 | g0104 | AFR | MSL | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG03486 | hp2 | a0002 | c0002 | t0019 | g0214 | AFR | MSL | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG03490 | hp1 | a0003 | c0004 | t0003 | g0173 | SAS | PJL | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG03490 | hp2 | a0001 | c0001 | t0004 | g0058 | SAS | PJL | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG03491 | hp2 | a0002 | c0002 | t0002 | g0046 | SAS | PJL | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG03492 | hp1 | a0002 | c0002 | t0002 | g0046 | SAS | PJL | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG03492 | hp2 | a0001 | c0001 | t0004 | g0063 | SAS | PJL | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG03540 | hp2 | a0004 | c0005 | t0005 | g0048 | AFR | GWD | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0258 | AFR | MSL | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0175 | AFR | MSL | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG03669 | hp1 | a0002 | c0002 | t0002 | g0232 | SAS | PJL | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG03669 | hp2 | a0002 | c0002 | t0002 | g0213 | SAS | PJL | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0200 | SAS | STU | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG03688 | hp2 | a0012 | c0012 | t0002 | g0188 | SAS | STU | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0017 | SAS | PJL | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG03704 | hp2 | a0006 | c0008 | t0002 | g0216 | SAS | PJL | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0017 | SAS | PJL | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG03710 | hp2 | a0013 | c0017 | t0003 | g0168 | SAS | PJL | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG03831 | hp1 | a0001 | c0001 | t0004 | g0055 | SAS | BEB | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0185 | SAS | BEB | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG03834 | hp1 | a0001 | c0001 | t0004 | g0081 | SAS | BEB | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG03834 | hp2 | a0002 | c0002 | t0002 | g0233 | SAS | BEB | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG03927 | hp1 | a0001 | c0003 | t0001 | g0128 | SAS | BEB | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0221 | SAS | BEB | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG04115 | hp2 | a0002 | c0002 | t0002 | g0021 | SAS | STU | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG04184 | hp1 | a0002 | c0020 | t0002 | g0230 | SAS | BEB | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0070 | SAS | BEB | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG04199 | hp1 | a0006 | c0008 | t0002 | g0215 | SAS | STU | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG04199 | hp2 | a0003 | c0004 | t0003 | g0047 | SAS | STU | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG04228 | hp1 | a0001 | c0001 | t0004 | g0054 | SAS | STU | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0004 | SAS | STU | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0181 | AFR | YRI | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0009 | AFR | YRI | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA18612 | hp1 | a0002 | c0002 | t0002 | g0217 | EAS | CHB | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | CHB | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA18747 | hp2 | a0001 | c0003 | t0001 | g0002 | EAS | CHB | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0174 | AFR | YRI | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | YRI | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0192 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA18940 | hp1 | a0001 | c0003 | t0001 | g0033 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA18940 | hp2 | a0003 | c0004 | t0003 | g0159 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA18944 | hp1 | a0001 | c0003 | t0001 | g0131 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA18946 | hp2 | a0002 | c0002 | t0002 | g0020 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA18948 | hp2 | a0001 | c0003 | t0001 | g0002 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA18949 | hp2 | a0002 | c0002 | t0002 | g0114 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA18954 | hp1 | a0001 | c0003 | t0001 | g0005 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA18957 | hp1 | a0001 | c0003 | t0001 | g0002 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA18960 | hp1 | a0001 | c0003 | t0001 | g0002 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA18961 | hp1 | a0002 | c0002 | t0002 | g0252 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA18962 | hp1 | a0002 | c0002 | t0002 | g0255 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA18966 | hp1 | a0002 | c0002 | t0002 | g0007 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA18969 | hp1 | a0002 | c0002 | t0002 | g0219 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA18970 | hp2 | a0002 | c0002 | t0002 | g0045 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA18971 | hp1 | a0002 | c0002 | t0002 | g0020 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA18971 | hp2 | a0015 | c0015 | t0001 | g0083 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA18973 | hp1 | a0002 | c0002 | t0002 | g0209 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA18973 | hp2 | a0002 | c0002 | t0002 | g0222 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA18975 | hp1 | a0002 | c0002 | t0002 | g0225 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA18975 | hp2 | a0002 | c0002 | t0002 | g0007 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA18977 | hp1 | a0002 | c0002 | t0002 | g0019 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA18979 | hp1 | a0002 | c0002 | t0002 | g0007 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA18980 | hp2 | a0002 | c0002 | t0002 | g0116 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA18982 | hp1 | a0001 | c0003 | t0001 | g0002 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA18985 | hp2 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA18988 | hp1 | a0003 | c0004 | t0003 | g0040 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA18988 | hp2 | a0002 | c0002 | t0002 | g0007 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA18990 | hp1 | a0003 | c0004 | t0003 | g0003 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0194 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA18993 | hp2 | a0002 | c0002 | t0002 | g0231 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA18994 | hp1 | a0001 | c0003 | t0001 | g0057 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA18994 | hp2 | a0003 | c0004 | t0003 | g0171 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA18995 | hp2 | a0003 | c0004 | t0003 | g0003 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA18997 | hp1 | a0001 | c0001 | t0021 | g0135 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA18997 | hp2 | a0002 | c0002 | t0002 | g0227 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA18998 | hp1 | a0001 | c0003 | t0001 | g0098 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA18998 | hp2 | a0002 | c0002 | t0002 | g0007 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA18999 | hp1 | a0002 | c0002 | t0002 | g0019 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA19002 | hp1 | a0001 | c0003 | t0001 | g0005 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA19004 | hp1 | a0001 | c0003 | t0001 | g0033 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA19004 | hp2 | a0002 | c0002 | t0002 | g0210 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0132 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA19005 | hp2 | a0001 | c0003 | t0001 | g0034 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA19007 | hp2 | a0003 | c0004 | t0003 | g0003 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA19009 | hp1 | a0002 | c0002 | t0002 | g0207 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA19011 | hp1 | a0003 | c0004 | t0003 | g0003 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | LWK | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA19030 | hp2 | a0004 | c0005 | t0005 | g0048 | AFR | LWK | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | LWK | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | LWK | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA19054 | hp2 | a0002 | c0002 | t0002 | g0256 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA19055 | hp2 | a0001 | c0001 | t0002 | g0197 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA19056 | hp1 | a0001 | c0003 | t0001 | g0005 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA19059 | hp1 | a0003 | c0004 | t0003 | g0267 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA19059 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA19060 | hp1 | a0001 | c0003 | t0001 | g0032 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA19060 | hp2 | a0002 | c0002 | t0002 | g0007 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA19062 | hp1 | a0001 | c0001 | t0011 | g0073 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA19062 | hp2 | a0001 | c0003 | t0001 | g0012 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA19065 | hp2 | a0002 | c0002 | t0002 | g0236 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA19066 | hp1 | a0002 | c0002 | t0002 | g0019 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0195 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA19075 | hp2 | a0001 | c0001 | t0002 | g0110 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA19080 | hp1 | a0002 | c0002 | t0002 | g0045 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA19080 | hp2 | a0003 | c0004 | t0003 | g0172 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA19081 | hp1 | a0001 | c0003 | t0001 | g0005 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA19083 | hp1 | a0002 | c0002 | t0002 | g0044 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA19083 | hp2 | a0001 | c0003 | t0001 | g0123 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA19084 | hp1 | a0001 | c0003 | t0001 | g0005 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA19084 | hp2 | a0002 | c0002 | t0002 | g0007 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA19086 | hp1 | a0002 | c0002 | t0002 | g0042 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA19086 | hp2 | a0001 | c0003 | t0001 | g0002 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA19087 | hp1 | a0002 | c0002 | t0002 | g0224 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA19087 | hp2 | a0003 | c0004 | t0003 | g0003 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA19088 | hp2 | a0002 | c0002 | t0002 | g0211 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA19089 | hp1 | a0003 | c0004 | t0003 | g0047 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA19089 | hp2 | a0001 | c0003 | t0001 | g0147 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA19091 | hp1 | a0002 | c0002 | t0002 | g0253 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA19091 | hp2 | a0001 | c0003 | t0001 | g0002 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0239 | AFR | YRI | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | YRI | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0009 | AFR | ASW | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0016 | AFR | ASW | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0017 | EUR | TSI | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA20752 | hp2 | a0001 | c0003 | t0014 | g0137 | EUR | TSI | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA20805 | hp1 | a0001 | c0001 | t0023 | g0183 | EUR | TSI | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA20805 | hp2 | a0001 | c0001 | t0004 | g0013 | EUR | TSI | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG01123 | hp1 | a0001 | c0003 | t0001 | g0012 | AMR | CLM | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG01123 | hp2 | a0003 | c0004 | t0003 | g0003 | AMR | CLM | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG02109 | hp1 | a0001 | c0001 | t0007 | g0141 | AFR | ACB | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0112 | AFR | ACB | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0178 | AFR | ACB | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | ACB | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0009 | AFR | MSL | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG03471 | hp2 | a0001 | c0001 | t0016 | g0102 | AFR | MSL | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG06807 | hp1 | a0003 | c0004 | t0003 | g0167 | AFR | USA | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | USA | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA18955 | hp1 | a0014 | c0009 | t0002 | g0196 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA18955 | hp2 | a0001 | c0003 | t0001 | g0130 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA21309 | hp1 | a0003 | c0004 | t0003 | g0015 | AFR | LWK | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0265 | AFR | LWK | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0176 | REF | REF | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| homoSapiens | grch38p0 | a0001 | c0006 | t0002 | g0270 | REF | REF | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:61826484 | C | T | 1 | a0009 | 1 | HG02965.hp1 | missense_variant | MODERATE | c.2122G>A | p.Glu708Lys | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 7/7 | 2141/3777 | 2122/2151 | 708/716 | chr2 | 61826484 | |||
| chr2:61827107 | T | A | 1 | a0012 | 1 | HG03688.hp2 | missense_variant | MODERATE | c.2003A>T | p.Glu668Val | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 6/7 | 2022/3777 | 2003/2151 | 668/716 | chr2 | 61827107 | |||
| chr2:61827151 | C | A | 1 | a0006 | 2 | HG03704.hp2 HG04199.hp1 |
missense_variant | MODERATE | c.1959G>T | p.Glu653Asp | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 6/7 | 1978/3777 | 1959/2151 | 653/716 | chr2 | 61827151 | |||
| chr2:61838634 | A | C | 2 | a0004 a0005 |
9 | HG02280.hp1 HG02451.hp1 HG02572.hp1 others(6): Show |
missense_variant | MODERATE | c.1655T>G | p.Met552Arg | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 4/7 | 1674/3777 | 1655/2151 | 552/716 | chr2 | 61838634 | |||
| chr2:61839520 | C | T | 1 | a0014 | 1 | NA18955.hp1 | missense_variant | MODERATE | c.1484G>A | p.Arg495His | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 3/7 | 1503/3777 | 1484/2151 | 495/716 | chr2 | 61839520 | |||
| chr2:61839871 | A | C | 1 | a0007 | 1 | HG01255.hp1 | missense_variant | MODERATE | c.1133T>G | p.Leu378Arg | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 3/7 | 1152/3777 | 1133/2151 | 378/716 | chr2 | 61839871 | |||
| chr2:61839895 | T | C | 1 | a0013 | 1 | HG03710.hp2 | missense_variant | MODERATE | c.1109A>G | p.Asn370Ser | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 3/7 | 1128/3777 | 1109/2151 | 370/716 | chr2 | 61839895 | |||
| chr2:61839991 | C | T | 1 | a0004 | 6 | HG02280.hp1 HG02451.hp1 HG03041.hp1 others(3): Show |
missense_variant | MODERATE | c.1013G>A | p.Arg338Gln | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 3/7 | 1032/3777 | 1013/2151 | 338/716 | chr2 | 61839991 | |||
| chr2:61840022 | T | C | 1 | a0008 | 1 | HG02572.hp2 | missense_variant | MODERATE | c.982A>G | p.Ile328Val | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 3/7 | 1001/3777 | 982/2151 | 328/716 | chr2 | 61840022 | |||
| chr2:61840088 | G | A | 1 | a0015 | 1 | NA18971.hp2 | missense_variant | MODERATE | c.916C>T | p.Arg306Trp | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 3/7 | 935/3777 | 916/2151 | 306/716 | chr2 | 61840088 | |||
| chr2:61840298 | T | C | 3 | a0003 a0007 a0013 |
39 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(36): Show |
missense_variant | MODERATE | c.706A>G | p.Ile236Val | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 3/7 | 725/3777 | 706/2151 | 236/716 | chr2 | 61840298 | |||
| chr2:61840406 | T | C | 1 | a0011 | 1 | HG03195.hp1 | missense_variant | MODERATE | c.598A>G | p.Asn200Asp | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 3/7 | 617/3777 | 598/2151 | 200/716 | chr2 | 61840406 | |||
| chr2:61842223 | T | C | 2 | a0002 a0006 |
70 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(67): Show |
missense_variant | MODERATE | c.321A>G | p.Ile107Met | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 2/7 | 340/3777 | 321/2151 | 107/716 | chr2 | 61842223 | |||
| chr2:61842347 | G | A | 1 | a0010 | 1 | HG03017.hp1 | missense_variant | MODERATE | c.197C>T | p.Thr66Ile | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 2/7 | 216/3777 | 197/2151 | 66/716 | chr2 | 61842347 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:61838624 | C | T | 2 | a0001c0003 a0010c0021 |
55 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(52): Show |
synonymous_variant | LOW | c.1665G>A | p.Leu555Leu | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 4/7 | 1684/3777 | 1665/2151 | 555/716 | chr2 | 61838624 | |||
| chr2:61839453 | C | T | 1 | a0005c0007 | 2 | HG02572.hp1 HG03130.hp2 |
synonymous_variant | LOW | c.1551G>A | p.Thr517Thr | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 3/7 | 1570/3777 | 1551/2151 | 517/716 | chr2 | 61839453 | |||
| chr2:61839462 | G | C | 1 | a0001c0013 | 1 | HG03486.hp1 | synonymous_variant | LOW | c.1542C>G | p.Pro514Pro | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 3/7 | 1561/3777 | 1542/2151 | 514/716 | chr2 | 61839462 | |||
| chr2:61839792 | A | G | 20 | a0001c0001 a0001c0003 a0001c0013 others(17): Show |
395 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(392): Show |
synonymous_variant | LOW | c.1212T>C | p.Cys404Cys | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 3/7 | 1231/3777 | 1212/2151 | 404/716 | chr2 | 61839792 | |||
| chr2:61840098 | T | C | 1 | a0011c0018 | 1 | HG03195.hp1 | synonymous_variant | LOW | c.906A>G | p.Gln302Gln | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 3/7 | 925/3777 | 906/2151 | 302/716 | chr2 | 61840098 | |||
| chr2:61840452 | C | T | 1 | a0002c0020 | 1 | HG04184.hp1 | synonymous_variant | LOW | c.552G>A | p.Glu184Glu | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 3/7 | 571/3777 | 552/2151 | 184/716 | chr2 | 61840452 | |||
| chr2:61840533 | T | C | 1 | a0001c0019 | 1 | HG03453.hp2 | synonymous_variant | LOW | c.471A>G | p.Ser157Ser | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 3/7 | 490/3777 | 471/2151 | 157/716 | chr2 | 61840533 | |||
| chr2:61853877 | A | C | 20 | a0001c0001 a0001c0003 a0001c0013 others(17): Show |
395 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(392): Show |
synonymous_variant | LOW | c.165T>G | p.Ala55Ala | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/7 | 184/3777 | 165/2151 | 55/716 | chr2 | 61853877 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:61824904 | T | G | 1 | a0001c0001t0008 | 2 | HG01515.hp1 HG01517.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1551A>C | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 7/7 | 1551 | chr2 | 61824904 | ||||||
| chr2:61824906 | C | A | 3 | a0004c0005t0005 a0005c0007t0009 a0005c0010t0018 |
8 | HG02280.hp1 HG02572.hp1 HG02622.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1549G>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 7/7 | 1549 | chr2 | 61824906 | ||||||
| chr2:61824974 | T | C | 1 | a0002c0002t0019 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1481A>G | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 7/7 | 1481 | chr2 | 61824974 | ||||||
| chr2:61824997 | C | T | 2 | a0001c0001t0007 a0001c0019t0007 |
2 | HG02109.hp1 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1458G>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 7/7 | 1458 | chr2 | 61824997 | ||||||
| chr2:61825023 | A | G | 1 | a0001c0001t0013 | 1 | HG02015.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1432T>C | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 7/7 | 1432 | chr2 | 61825023 | ||||||
| chr2:61825087 | T | G | 1 | a0001c0003t0014 | 1 | NA20752.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1368A>C | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 7/7 | 1368 | chr2 | 61825087 | ||||||
| chr2:61825174 | A | G | 1 | a0001c0001t0016 | 1 | HG03471.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1281T>C | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 7/7 | 1281 | chr2 | 61825174 | ||||||
| chr2:61825245 | A | G | 16 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0006 others(13): Show |
206 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(203): Show |
3_prime_UTR_variant | MODIFIER | c.*1210T>C | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 7/7 | 1210 | chr2 | 61825245 | ||||||
| chr2:61825311 | A | C | 1 | a0002c0002t0012 | 1 | HG02145.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1144T>G | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 7/7 | 1144 | chr2 | 61825311 | ||||||
| chr2:61825485 | T | C | 1 | a0001c0001t0020 | 1 | HG02886.hp2 | 3_prime_UTR_variant | MODIFIER | c.*970A>G | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 7/7 | 970 | chr2 | 61825485 | ||||||
| chr2:61825564 | T | C | 1 | a0001c0001t0021 | 1 | NA18997.hp1 | 3_prime_UTR_variant | MODIFIER | c.*891A>G | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 7/7 | 891 | chr2 | 61825564 | ||||||
| chr2:61825626 | A | G | 1 | a0001c0001t0016 | 1 | HG03471.hp2 | 3_prime_UTR_variant | MODIFIER | c.*829T>C | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 7/7 | 829 | chr2 | 61825626 | ||||||
| chr2:61825679 | C | T | 1 | a0011c0018t0015 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*776G>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 7/7 | 776 | chr2 | 61825679 | ||||||
| chr2:61825782 | C | T | 1 | a0001c0001t0011 | 1 | NA19062.hp1 | 3_prime_UTR_variant | MODIFIER | c.*673G>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 7/7 | 673 | chr2 | 61825782 | ||||||
| chr2:61825838 | C | T | 1 | a0001c0001t0006 | 2 | HG02258.hp2 HG03130.hp1 |
3_prime_UTR_variant | MODIFIER | c.*617G>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 7/7 | 617 | chr2 | 61825838 | ||||||
| chr2:61825915 | G | C | 1 | a0005c0007t0009 | 2 | HG02572.hp1 HG03130.hp2 |
3_prime_UTR_variant | MODIFIER | c.*540C>G | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 7/7 | 540 | chr2 | 61825915 | ||||||
| chr2:61825946 | T | G | 1 | a0001c0001t0022 | 1 | HG00597.hp1 | 3_prime_UTR_variant | MODIFIER | c.*509A>C | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 7/7 | 509 | chr2 | 61825946 | ||||||
| chr2:61826144 | T | G | 3 | a0003c0004t0003 a0007c0016t0003 a0013c0017t0003 |
39 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*311A>C | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 7/7 | 311 | chr2 | 61826144 | ||||||
| chr2:61826155 | A | G | 15 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0006 others(12): Show |
205 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(202): Show |
3_prime_UTR_variant | MODIFIER | c.*300T>C | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 7/7 | 300 | chr2 | 61826155 | ||||||
| chr2:61826206 | TA | T | 3 | a0003c0004t0003 a0007c0016t0003 a0013c0017t0003 |
39 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*248delT | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 7/7 | 248 | chr2 | 61826206 | ||||||
| chr2:61826247 | G | C | 1 | a0001c0001t0024 | 1 | HG00323.hp1 | 3_prime_UTR_variant | MODIFIER | c.*208C>G | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 7/7 | 208 | chr2 | 61826247 | ||||||
| chr2:61826395 | G | A | 1 | a0001c0001t0023 | 1 | NA20805.hp1 | 3_prime_UTR_variant | MODIFIER | c.*60C>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 7/7 | 60 | chr2 | 61826395 | ||||||
| chr2:61826411 | CGCT | C | 3 | a0001c0001t0004 a0001c0001t0024 a0010c0021t0004 |
21 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*41_*43delAGC | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 7/7 | 41 | chr2 | 61826411 | ||||||
| chr2:61826429 | G | A | 1 | a0004c0005t0005 | 5 | HG02280.hp1 HG03041.hp1 HG03453.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*26C>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 7/7 | 26 | chr2 | 61826429 | ||||||
| chr2:61854057 | G | C | 1 | a0001c0001t0010 | 2 | HG02922.hp1 HG02970.hp2 |
5_prime_UTR_variant | MODIFIER | c.-16C>G | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/7 | 16 | chr2 | 61854057 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:61826743 | G | GA | 268 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(265): Show |
395 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(392): Show |
intron_variant | MODIFIER | c.2007-145dupT | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 6/6 | chr2 | 61826743 | |||||||
| chr2:61826847 | G | A | 2 | a0001c0001t0001g0107 a0001c0001t0001g0108 |
2 | HG01243.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2007-248C>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 6/6 | chr2 | 61826847 | |||||||
| chr2:61826934 | C | T | 36 | a0001c0001t0002g0004 a0001c0001t0002g0016 a0001c0001t0002g0017 others(33): Show |
49 | HG00597.hp1 HG01109.hp1 HG01167.hp2 others(46): Show |
intron_variant | MODIFIER | c.2006+170G>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 6/6 | chr2 | 61826934 | |||||||
| chr2:61827444 | A | T | 1 | a0001c0001t0001g0108 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1852-186T>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61827444 | |||||||
| chr2:61827500 | C | T | 1 | a0009c0011t0002g0247 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1852-242G>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61827500 | |||||||
| chr2:61827526 | C | T | 1 | a0001c0001t0002g0258 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1852-268G>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61827526 | |||||||
| chr2:61827541 | C | T | 1 | a0002c0002t0002g0210 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1852-283G>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61827541 | |||||||
| chr2:61827609 | C | CA | 193 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0014 others(190): Show |
284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.1852-352dupT | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61827609 | |||||||
| chr2:61827609 | C | CAA | 27 | a0001c0001t0001g0008 a0001c0001t0001g0030 a0001c0001t0001g0076 others(24): Show |
34 | HG00323.hp2 HG00558.hp2 HG01175.hp2 others(31): Show |
intron_variant | MODIFIER | c.1852-353_1852-352d others(4): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61827609 | |||||||
| chr2:61827630 | T | A | 32 | a0001c0001t0001g0006 a0001c0001t0001g0120 a0001c0001t0001g0139 others(29): Show |
64 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(61): Show |
intron_variant | MODIFIER | c.1852-372A>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61827630 | |||||||
| chr2:61827813 | G | A | 1 | a0001c0006t0002g0269 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1852-555C>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61827813 | |||||||
| chr2:61828002 | T | C | 37 | a0001c0001t0002g0004 a0001c0001t0002g0016 a0001c0001t0002g0017 others(34): Show |
52 | HG00597.hp1 HG01109.hp1 HG01167.hp2 others(49): Show |
intron_variant | MODIFIER | c.1852-744A>G | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61828002 | |||||||
| chr2:61828253 | T | C | 2 | a0001c0001t0002g0174 a0001c0001t0002g0175 |
2 | HG03579.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1852-995A>G | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61828253 | |||||||
| chr2:61828284 | GA | G | 252 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(249): Show |
376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.1852-1027delT | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61828284 | |||||||
| chr2:61828323 | A | AG | 5 | a0001c0001t0002g0016 a0001c0001t0002g0177 a0001c0001t0002g0181 others(2): Show |
7 | HG02055.hp2 HG02615.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1852-1066dupC | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61828323 | |||||||
| chr2:61828336 | C | CT | 42 | a0001c0001t0001g0099 a0001c0001t0001g0122 a0001c0001t0001g0144 others(39): Show |
57 | HG00597.hp1 HG00735.hp1 HG01109.hp1 others(54): Show |
intron_variant | MODIFIER | c.1852-1079dupA | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61828336 | |||||||
| chr2:61828552 | T | G | 5 | a0001c0001t0002g0035 a0001c0001t0002g0132 a0001c0001t0002g0134 others(2): Show |
6 | HG00597.hp1 HG02080.hp1 NA18980.hp1 others(3): Show |
intron_variant | MODIFIER | c.1852-1294A>C | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61828552 | |||||||
| chr2:61828732 | T | C | 1 | a0001c0001t0001g0108 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1852-1474A>G | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61828732 | |||||||
| chr2:61828843 | T | A | 1 | a0003c0004t0003g0167 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1852-1585A>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61828843 | |||||||
| chr2:61828912 | T | C | 3 | a0002c0002t0002g0204 a0002c0002t0002g0208 a0002c0002t0019g0214 |
3 | HG02647.hp1 HG02723.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1852-1654A>G | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61828912 | |||||||
| chr2:61829010 | G | A | 2 | a0001c0001t0001g0050 a0001c0001t0001g0259 |
3 | HG02280.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1852-1752C>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61829010 | |||||||
| chr2:61829131 | C | T | 3 | a0001c0001t0001g0023 a0001c0001t0001g0070 a0001c0001t0001g0071 |
4 | HG00673.hp2 HG04184.hp2 NA19068.hp1 others(1): Show |
intron_variant | MODIFIER | c.1852-1873G>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61829131 | |||||||
| chr2:61829212 | T | C | 1 | a0001c0006t0002g0269 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1852-1954A>G | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61829212 | |||||||
| chr2:61829294 | G | C | 1 | a0006c0008t0002g0215 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1852-2036C>G | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61829294 | |||||||
| chr2:61829347 | T | A | 1 | a0010c0021t0004g0084 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1852-2089A>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61829347 | |||||||
| chr2:61829378 | C | G | 1 | a0001c0003t0001g0128 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1852-2120G>C | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61829378 | |||||||
| chr2:61829685 | TA | T | 6 | a0001c0001t0001g0037 a0001c0001t0001g0056 a0001c0001t0001g0068 others(3): Show |
7 | NA18945.hp1 NA18945.hp2 NA19055.hp1 others(4): Show |
intron_variant | MODIFIER | c.1852-2428delT | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61829685 | |||||||
| chr2:61829978 | T | TA | 65 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0002g0009 others(62): Show |
84 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.1852-2721dupT | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61829978 | |||||||
| chr2:61829997 | C | T | 268 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(265): Show |
395 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(392): Show |
intron_variant | MODIFIER | c.1852-2739G>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61829997 | |||||||
| chr2:61830116 | T | A | 1 | a0009c0011t0002g0247 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1852-2858A>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61830116 | |||||||
| chr2:61830182 | G | A | 60 | a0001c0001t0002g0009 a0001c0001t0002g0112 a0001c0001t0002g0205 others(57): Show |
81 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.1852-2924C>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61830182 | |||||||
| chr2:61830245 | A | C | 3 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0017g0117 |
3 | HG01243.hp1 HG02886.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1852-2987T>G | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61830245 | |||||||
| chr2:61830413 | G | A | 38 | a0001c0001t0002g0004 a0001c0001t0002g0016 a0001c0001t0002g0017 others(35): Show |
53 | HG00597.hp1 HG01109.hp1 HG01167.hp2 others(50): Show |
intron_variant | MODIFIER | c.1852-3155C>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61830413 | |||||||
| chr2:61830510 | G | A | 1 | a0001c0001t0001g0108 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1852-3252C>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61830510 | |||||||
| chr2:61830633 | G | A | 37 | a0001c0001t0002g0004 a0001c0001t0002g0016 a0001c0001t0002g0017 others(34): Show |
50 | HG00597.hp1 HG01109.hp1 HG01167.hp2 others(47): Show |
intron_variant | MODIFIER | c.1852-3375C>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61830633 | |||||||
| chr2:61830678 | T | A | 4 | a0001c0001t0001g0022 a0001c0001t0001g0094 a0001c0001t0001g0095 others(1): Show |
5 | HG01167.hp1 HG01169.hp2 HG01243.hp2 others(2): Show |
intron_variant | MODIFIER | c.1852-3420A>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61830678 | |||||||
| chr2:61830683 | C | CA | 59 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0002g0004 others(56): Show |
83 | HG00408.hp1 HG00597.hp1 HG00639.hp2 others(80): Show |
intron_variant | MODIFIER | c.1852-3426dupT | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61830683 | |||||||
| chr2:61830683 | C | CAA | 130 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(127): Show |
212 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(209): Show |
intron_variant | MODIFIER | c.1852-3427_1852-342 others(6): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61830683 | |||||||
| chr2:61830683 | C | CAAA | 26 | a0001c0001t0001g0030 a0001c0001t0001g0053 a0001c0001t0001g0067 others(23): Show |
31 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(28): Show |
intron_variant | MODIFIER | c.1852-3428_1852-342 others(7): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61830683 | |||||||
| chr2:61830833 | G | A | 37 | a0001c0001t0002g0004 a0001c0001t0002g0016 a0001c0001t0002g0017 others(34): Show |
52 | HG00597.hp1 HG01109.hp1 HG01167.hp2 others(49): Show |
intron_variant | MODIFIER | c.1852-3575C>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61830833 | |||||||
| chr2:61830955 | A | G | 1 | a0001c0001t0016g0102 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1852-3697T>C | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61830955 | |||||||
| chr2:61831067 | G | A | 3 | a0001c0001t0002g0186 a0001c0001t0002g0248 a0001c0001t0017g0117 |
3 | HG01891.hp2 HG02451.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1852-3809C>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61831067 | |||||||
| chr2:61831111 | C | CA | 23 | a0003c0004t0003g0003 a0003c0004t0003g0015 a0003c0004t0003g0031 others(20): Show |
36 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(33): Show |
intron_variant | MODIFIER | c.1852-3854dupT | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61831111 | |||||||
| chr2:61831111 | CA | C | 207 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(204): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(311): Show |
intron_variant | MODIFIER | c.1852-3854delT | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61831111 | |||||||
| chr2:61831216 | T | C | 1 | a0001c0001t0002g0266 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1852-3958A>G | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61831216 | |||||||
| chr2:61831261 | G | C | 1 | a0001c0001t0002g0266 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1852-4003C>G | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61831261 | |||||||
| chr2:61831343 | G | C | 1 | a0009c0011t0002g0247 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1852-4085C>G | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61831343 | |||||||
| chr2:61831407 | C | T | 3 | a0001c0001t0001g0014 a0001c0001t0001g0103 a0001c0001t0001g0111 |
5 | HG01891.hp1 HG02145.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1852-4149G>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61831407 | |||||||
| chr2:61831506 | T | C | 1 | a0003c0004t0003g0160 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1852-4248A>G | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61831506 | |||||||
| chr2:61831970 | G | A | 1 | a0001c0001t0002g0258 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1851+4040C>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61831970 | |||||||
| chr2:61832023 | T | A | 3 | a0001c0003t0001g0033 a0001c0003t0001g0098 a0001c0003t0014g0137 |
4 | NA18940.hp1 NA18998.hp1 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.1851+3987A>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61832023 | |||||||
| chr2:61832151 | G | A | 1 | a0003c0004t0003g0160 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1851+3859C>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61832151 | |||||||
| chr2:61832242 | C | CA | 86 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(83): Show |
154 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.1851+3767dupT | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61832242 | |||||||
| chr2:61832242 | C | CAA | 36 | a0001c0001t0001g0026 a0001c0001t0001g0030 a0001c0001t0001g0053 others(33): Show |
42 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(39): Show |
intron_variant | MODIFIER | c.1851+3767_1851+376 others(6): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61832242 | |||||||
| chr2:61832244 | C | A | 128 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(125): Show |
202 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(199): Show |
intron_variant | MODIFIER | c.1851+3766G>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61832244 | |||||||
| chr2:61832246 | C | A | 128 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(125): Show |
202 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(199): Show |
intron_variant | MODIFIER | c.1851+3764G>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61832246 | |||||||
| chr2:61832248 | C | A | 128 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(125): Show |
202 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(199): Show |
intron_variant | MODIFIER | c.1851+3762G>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61832248 | |||||||
| chr2:61832250 | C | A | 154 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(151): Show |
241 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(238): Show |
intron_variant | MODIFIER | c.1851+3760G>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61832250 | |||||||
| chr2:61832252 | A | C | 41 | a0001c0001t0001g0014 a0001c0001t0001g0103 a0001c0001t0002g0004 others(38): Show |
56 | HG00597.hp1 HG01109.hp1 HG01167.hp2 others(53): Show |
intron_variant | MODIFIER | c.1851+3758T>G | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61832252 | |||||||
| chr2:61832263 | A | C | 61 | a0001c0001t0002g0009 a0001c0001t0002g0112 a0001c0001t0002g0205 others(58): Show |
84 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.1851+3747T>G | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61832263 | |||||||
| chr2:61832266 | A | C | 25 | a0002c0002t0002g0019 a0002c0002t0002g0020 a0002c0002t0002g0043 others(22): Show |
31 | HG00323.hp2 HG00408.hp1 HG01943.hp1 others(28): Show |
intron_variant | MODIFIER | c.1851+3744T>G | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61832266 | |||||||
| chr2:61832296 | A | C | 2 | a0001c0001t0001g0155 a0001c0001t0016g0102 |
2 | HG02165.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1851+3714T>G | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61832296 | |||||||
| chr2:61832808 | T | C | 268 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(265): Show |
395 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(392): Show |
intron_variant | MODIFIER | c.1851+3202A>G | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61832808 | |||||||
| chr2:61832832 | C | T | 1 | a0001c0006t0002g0271 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1851+3178G>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61832832 | |||||||
| chr2:61832849 | G | A | 1 | a0001c0001t0002g0258 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1851+3161C>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61832849 | |||||||
| chr2:61832866 | A | G | 1 | a0009c0011t0002g0247 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1851+3144T>C | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61832866 | |||||||
| chr2:61833121 | T | A | 100 | a0001c0001t0002g0004 a0001c0001t0002g0009 a0001c0001t0002g0016 others(97): Show |
136 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.1851+2889A>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61833121 | |||||||
| chr2:61833289 | G | A | 1 | a0002c0002t0002g0256 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.1851+2721C>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61833289 | |||||||
| chr2:61833295 | G | A | 2 | a0001c0001t0004g0059 a0001c0001t0004g0092 |
2 | HG00735.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.1851+2715C>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61833295 | |||||||
| chr2:61833425 | C | CA | 34 | a0001c0001t0002g0206 a0001c0001t0002g0251 a0001c0001t0002g0260 others(31): Show |
47 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(44): Show |
intron_variant | MODIFIER | c.1851+2584dupT | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61833425 | |||||||
| chr2:61833425 | CA | C | 6 | a0001c0001t0001g0014 a0001c0001t0001g0103 a0001c0001t0001g0111 others(3): Show |
8 | HG01891.hp1 HG02145.hp2 HG02165.hp2 others(5): Show |
intron_variant | MODIFIER | c.1851+2584delT | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61833425 | |||||||
| chr2:61833425 | CAA | C | 121 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(118): Show |
195 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(192): Show |
intron_variant | MODIFIER | c.1851+2583_1851+258 others(6): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61833425 | |||||||
| chr2:61833457 | A | G | 5 | a0001c0001t0002g0035 a0001c0001t0002g0132 a0001c0001t0002g0134 others(2): Show |
6 | HG00597.hp1 HG02080.hp1 NA18980.hp1 others(3): Show |
intron_variant | MODIFIER | c.1851+2553T>C | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61833457 | |||||||
| chr2:61833510 | C | G | 121 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(118): Show |
194 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(191): Show |
intron_variant | MODIFIER | c.1851+2500G>C | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61833510 | |||||||
| chr2:61833511 | C | T | 254 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(251): Show |
377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.1851+2499G>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61833511 | |||||||
| chr2:61833593 | C | T | 4 | a0002c0002t0002g0007 a0002c0002t0002g0207 a0002c0002t0002g0252 others(1): Show |
10 | NA18961.hp1 NA18966.hp1 NA18975.hp2 others(7): Show |
intron_variant | MODIFIER | c.1851+2417G>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61833593 | |||||||
| chr2:61833622 | C | T | 2 | a0001c0001t0004g0058 a0001c0001t0004g0063 |
2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1851+2388G>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61833622 | |||||||
| chr2:61833671 | C | G | 26 | a0003c0004t0003g0003 a0003c0004t0003g0015 a0003c0004t0003g0031 others(23): Show |
39 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(36): Show |
intron_variant | MODIFIER | c.1851+2339G>C | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61833671 | |||||||
| chr2:61833714 | C | T | 1 | a0009c0011t0002g0247 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1851+2296G>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61833714 | |||||||
| chr2:61833736 | AAGAC | A | 123 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(120): Show |
197 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.1851+2270_1851+227 others(8): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61833736 | |||||||
| chr2:61833757 | C | G | 1 | a0001c0001t0002g0199 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1851+2253G>C | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61833757 | |||||||
| chr2:61833820 | A | T | 2 | a0001c0001t0010g0272 a0001c0001t0010g0273 |
2 | HG02922.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1851+2190T>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61833820 | |||||||
| chr2:61834226 | T | C | 123 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(120): Show |
197 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.1851+1784A>G | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61834226 | |||||||
| chr2:61834269 | T | C | 123 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(120): Show |
197 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.1851+1741A>G | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61834269 | |||||||
| chr2:61834410 | A | C | 3 | a0001c0001t0002g0260 a0001c0001t0002g0265 a0001c0001t0002g0266 |
3 | HG02630.hp1 HG03098.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1851+1600T>G | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61834410 | |||||||
| chr2:61834624 | G | A | 1 | a0001c0001t0002g0266 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1851+1386C>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61834624 | |||||||
| chr2:61834689 | C | T | 1 | a0011c0018t0015g0261 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1851+1321G>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61834689 | |||||||
| chr2:61834786 | C | T | 3 | a0001c0001t0001g0014 a0001c0001t0001g0103 a0001c0001t0001g0111 |
5 | HG01891.hp1 HG02145.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1851+1224G>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61834786 | |||||||
| chr2:61834791 | A | C | 1 | a0002c0002t0002g0217 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1851+1219T>G | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61834791 | |||||||
| chr2:61834808 | A | T | 63 | a0001c0001t0002g0009 a0001c0001t0002g0112 a0001c0001t0002g0205 others(60): Show |
86 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.1851+1202T>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61834808 | |||||||
| chr2:61834821 | A | AAAAT | 4 | a0001c0001t0001g0107 a0001c0001t0002g0174 a0001c0001t0002g0175 others(1): Show |
4 | HG02886.hp1 HG03579.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1851+1185_1851+118 others(8): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61834821 | |||||||
| chr2:61835066 | C | T | 126 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(123): Show |
200 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(197): Show |
intron_variant | MODIFIER | c.1851+944G>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61835066 | |||||||
| chr2:61835080 | A | G | 1 | a0011c0018t0015g0261 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1851+930T>C | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61835080 | |||||||
| chr2:61835468 | TA | T | 36 | a0001c0001t0002g0004 a0001c0001t0002g0016 a0001c0001t0002g0017 others(33): Show |
49 | HG00597.hp1 HG01109.hp1 HG01167.hp2 others(46): Show |
intron_variant | MODIFIER | c.1851+541delT | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61835468 | |||||||
| chr2:61835883 | C | T | 1 | a0001c0001t0002g0266 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1851+127G>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61835883 | |||||||
| chr2:61835884 | A | C | 1 | a0001c0001t0002g0266 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1851+126T>G | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61835884 | |||||||
| chr2:61835958 | TA | T | 234 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(231): Show |
355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
intron_variant | MODIFIER | c.1851+51delT | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61835958 | |||||||
| chr2:61835958 | TAA | T | 7 | a0001c0001t0001g0024 a0001c0001t0001g0068 a0001c0001t0001g0069 others(4): Show |
8 | HG00423.hp1 HG01070.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.1851+50_1851+51del others(2): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61835958 | |||||||
| chr2:61835972 | A | C | 1 | a0001c0001t0001g0108 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1851+38T>G | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61835972 | |||||||
| chr2:61836206 | TG | T | 37 | a0001c0001t0002g0004 a0001c0001t0002g0016 a0001c0001t0002g0017 others(34): Show |
50 | HG00597.hp1 HG01109.hp1 HG01167.hp2 others(47): Show |
intron_variant | MODIFIER | c.1752-98delC | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 4/6 | chr2 | 61836206 | |||||||
| chr2:61836290 | T | C | 1 | a0001c0003t0001g0131 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1752-181A>G | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 4/6 | chr2 | 61836290 | |||||||
| chr2:61836452 | G | T | 1 | a0009c0011t0002g0247 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1752-343C>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 4/6 | chr2 | 61836452 | |||||||
| chr2:61836512 | T | C | 8 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0026 others(5): Show |
12 | HG00408.hp2 HG00544.hp1 HG02071.hp1 others(9): Show |
intron_variant | MODIFIER | c.1752-403A>G | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 4/6 | chr2 | 61836512 | |||||||
| chr2:61836761 | T | A | 37 | a0001c0001t0001g0006 a0001c0001t0001g0120 a0001c0001t0001g0139 others(34): Show |
71 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(68): Show |
intron_variant | MODIFIER | c.1752-652A>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 4/6 | chr2 | 61836761 | |||||||
| chr2:61836898 | C | T | 3 | a0004c0005t0002g0249 a0004c0005t0005g0048 a0004c0005t0005g0250 |
4 | HG02451.hp1 HG03041.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1752-789G>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 4/6 | chr2 | 61836898 | |||||||
| chr2:61836935 | G | A | 1 | a0001c0001t0001g0103 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1752-826C>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 4/6 | chr2 | 61836935 | |||||||
| chr2:61836952 | A | C | 1 | a0001c0001t0001g0068 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1752-843T>G | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 4/6 | chr2 | 61836952 | |||||||
| chr2:61837038 | T | A | 5 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0157 others(2): Show |
5 | HG01243.hp1 HG03579.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.1752-929A>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 4/6 | chr2 | 61837038 | |||||||
| chr2:61837150 | G | A | 1 | a0010c0021t0004g0084 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1752-1041C>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 4/6 | chr2 | 61837150 | |||||||
| chr2:61837269 | C | T | 254 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(251): Show |
377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.1752-1160G>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 4/6 | chr2 | 61837269 | |||||||
| chr2:61837530 | A | G | 1 | a0005c0010t0018g0262 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1751+1008T>C | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 4/6 | chr2 | 61837530 | |||||||
| chr2:61837535 | A | G | 254 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(251): Show |
377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.1751+1003T>C | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 4/6 | chr2 | 61837535 | |||||||
| chr2:61837629 | C | T | 1 | a0001c0001t0002g0174 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1751+909G>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 4/6 | chr2 | 61837629 | |||||||
| chr2:61837662 | T | C | 36 | a0001c0001t0002g0004 a0001c0001t0002g0016 a0001c0001t0002g0017 others(33): Show |
49 | HG00597.hp1 HG01109.hp1 HG01167.hp2 others(46): Show |
intron_variant | MODIFIER | c.1751+876A>G | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 4/6 | chr2 | 61837662 | |||||||
| chr2:61837667 | G | A | 1 | a0001c0001t0002g0266 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1751+871C>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 4/6 | chr2 | 61837667 | |||||||
| chr2:61837674 | C | A | 123 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(120): Show |
197 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.1751+864G>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 4/6 | chr2 | 61837674 | |||||||
| chr2:61837818 | C | T | 9 | a0001c0001t0001g0010 a0001c0001t0001g0022 a0001c0001t0001g0051 others(6): Show |
13 | HG00642.hp2 HG01074.hp2 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.1751+720G>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 4/6 | chr2 | 61837818 | |||||||
| chr2:61837914 | A | G | 1 | a0001c0003t0001g0057 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1751+624T>C | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 4/6 | chr2 | 61837914 | |||||||
| chr2:61838033 | A | G | 254 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(251): Show |
377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.1751+505T>C | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 4/6 | chr2 | 61838033 | |||||||
| chr2:61838390 | A | G | 268 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(265): Show |
395 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(392): Show |
intron_variant | MODIFIER | c.1751+148T>C | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 4/6 | chr2 | 61838390 | |||||||
| chr2:61838419 | A | T | 1 | a0002c0002t0002g0213 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1751+119T>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 4/6 | chr2 | 61838419 | |||||||
| chr2:61838716 | C | T | 28 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0003c0004t0003g0003 others(25): Show |
41 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(38): Show |
intron_variant | MODIFIER | c.1584-11G>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 3/6 | chr2 | 61838716 | |||||||
| chr2:61838854 | A | ATATT | 108 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0030 others(105): Show |
168 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.1584-153_1584-150d others(6): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 3/6 | chr2 | 61838854 | |||||||
| chr2:61838854 | A | ATATTTAT others(1): Show |
50 | a0001c0001t0001g0066 a0001c0001t0001g0149 a0001c0001t0001g0150 others(47): Show |
69 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(66): Show |
intron_variant | MODIFIER | c.1584-157_1584-150d others(10): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 3/6 | chr2 | 61838854 | |||||||
| chr2:61838854 | A | ATATTTAT others(5): Show |
2 | a0001c0001t0001g0107 a0003c0004t0003g0100 |
2 | HG02132.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1584-161_1584-150d others(14): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 3/6 | chr2 | 61838854 | |||||||
| chr2:61838854 | ATATTTAT others(1): Show |
A | 52 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0022 others(49): Show |
82 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.1584-157_1584-150d others(10): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 3/6 | chr2 | 61838854 | |||||||
| chr2:61838888 | A | ATTTT | 5 | a0001c0001t0002g0134 a0001c0001t0002g0186 a0001c0001t0002g0198 others(2): Show |
5 | HG01891.hp2 HG02080.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1584-184_1584-183i others(6): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 3/6 | chr2 | 61838888 | |||||||
| chr2:61838888 | A | T | 6 | a0001c0001t0001g0023 a0001c0001t0001g0060 a0001c0001t0001g0069 others(3): Show |
6 | HG00423.hp1 HG01243.hp1 NA18948.hp1 others(3): Show |
intron_variant | MODIFIER | c.1584-183T>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 3/6 | chr2 | 61838888 | |||||||
| chr2:61838892 | A | ATTTATTT others(5): Show |
2 | a0005c0007t0009g0264 a0005c0010t0018g0262 |
2 | HG02572.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.1584-188_1584-187i others(14): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 3/6 | chr2 | 61838892 | |||||||
| chr2:61838892 | A | ATTTATTT others(1): Show |
4 | a0001c0001t0002g0017 a0001c0001t0002g0179 a0001c0001t0002g0200 others(1): Show |
6 | HG01175.hp2 HG03579.hp1 HG03688.hp1 others(3): Show |
intron_variant | MODIFIER | c.1584-188_1584-187i others(10): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 3/6 | chr2 | 61838892 | |||||||
| chr2:61838892 | A | ATTTATTT others(5): Show |
1 | a0005c0007t0009g0263 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1584-188_1584-187i others(14): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 3/6 | chr2 | 61838892 | |||||||
| chr2:61838892 | A | ATTTT | 23 | a0001c0001t0002g0004 a0001c0001t0002g0016 a0001c0001t0002g0035 others(20): Show |
34 | HG00597.hp1 HG01109.hp1 HG01167.hp2 others(31): Show |
intron_variant | MODIFIER | c.1584-191_1584-188d others(6): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 3/6 | chr2 | 61838892 | |||||||
| chr2:61838892 | A | T | 47 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0022 others(44): Show |
72 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(69): Show |
intron_variant | MODIFIER | c.1584-187T>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 3/6 | chr2 | 61838892 | |||||||
| chr2:61838896 | T | A | 59 | a0001c0001t0002g0009 a0001c0001t0002g0112 a0001c0001t0002g0205 others(56): Show |
81 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.1584-191A>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 3/6 | chr2 | 61838896 | |||||||
| chr2:61838943 | C | T | 2 | a0001c0001t0002g0174 a0001c0001t0002g0175 |
2 | HG03579.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1584-238G>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 3/6 | chr2 | 61838943 | |||||||
| chr2:61838974 | C | T | 26 | a0001c0001t0001g0008 a0001c0001t0001g0030 a0001c0001t0001g0036 others(23): Show |
35 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(32): Show |
intron_variant | MODIFIER | c.1584-269G>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 3/6 | chr2 | 61838974 | |||||||
| chr2:61839010 | G | A | 1 | a0001c0001t0002g0182 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1584-305C>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 3/6 | chr2 | 61839010 | |||||||
| chr2:61839029 | C | T | 1 | a0001c0001t0017g0117 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1584-324G>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 3/6 | chr2 | 61839029 | |||||||
| chr2:61839031 | C | T | 2 | a0001c0001t0001g0050 a0001c0001t0001g0259 |
3 | HG02280.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1584-326G>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 3/6 | chr2 | 61839031 | |||||||
| chr2:61839089 | C | A | 1 | a0011c0018t0015g0261 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1583+332G>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 3/6 | chr2 | 61839089 | |||||||
| chr2:61839280 | T | C | 1 | a0009c0011t0002g0247 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1583+141A>G | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 3/6 | chr2 | 61839280 | |||||||
| chr2:61839282 | ATATAT | A | 131 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(128): Show |
206 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(203): Show |
intron_variant | MODIFIER | c.1583+134_1583+138d others(7): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 3/6 | chr2 | 61839282 | |||||||
| chr2:61839417 | T | C | 1 | a0001c0001t0001g0107 | 1 | NA19030.hp1 | splice_region_variant&intron_variant | LOW | c.1583+4A>G | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 3/6 | chr2 | 61839417 | |||||||
| chr2:61840588 | G | A | 2 | a0001c0001t0002g0258 a0009c0011t0002g0247 |
2 | HG02965.hp1 HG03579.hp1 |
splice_region_variant&intron_variant | LOW | c.423-7C>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 2/6 | chr2 | 61840588 | |||||||
| chr2:61840619 | T | C | 4 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0002g0174 others(1): Show |
4 | HG01243.hp1 HG03579.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.423-38A>G | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 2/6 | chr2 | 61840619 | |||||||
| chr2:61840621 | T | A | 1 | a0003c0004t0003g0169 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.423-40A>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 2/6 | chr2 | 61840621 | |||||||
| chr2:61840745 | G | C | 126 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(123): Show |
200 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(197): Show |
intron_variant | MODIFIER | c.423-164C>G | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 2/6 | chr2 | 61840745 | |||||||
| chr2:61840794 | G | A | 1 | a0002c0002t0002g0046 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.423-213C>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 2/6 | chr2 | 61840794 | |||||||
| chr2:61841036 | T | G | 4 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0002g0174 others(1): Show |
4 | HG01243.hp1 HG03579.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.423-455A>C | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 2/6 | chr2 | 61841036 | |||||||
| chr2:61841041 | C | A | 1 | a0003c0004t0003g0169 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.423-460G>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 2/6 | chr2 | 61841041 | |||||||
| chr2:61841169 | G | A | 5 | a0001c0001t0002g0035 a0001c0001t0002g0132 a0001c0001t0002g0134 others(2): Show |
6 | HG00597.hp1 HG02080.hp1 NA18980.hp1 others(3): Show |
intron_variant | MODIFIER | c.423-588C>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 2/6 | chr2 | 61841169 | |||||||
| chr2:61841517 | T | C | 1 | a0011c0018t0015g0261 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.422+605A>G | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 2/6 | chr2 | 61841517 | |||||||
| chr2:61841580 | T | C | 1 | a0001c0001t0002g0199 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.422+542A>G | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 2/6 | chr2 | 61841580 | |||||||
| chr2:61842008 | G | A | 1 | a0001c0001t0002g0266 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.422+114C>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 2/6 | chr2 | 61842008 | |||||||
| chr2:61842377 | A | C | 1 | a0001c0001t0017g0117 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.184-17T>G | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61842377 | |||||||
| chr2:61842391 | G | T | 1 | a0002c0002t0002g0228 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.184-31C>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61842391 | |||||||
| chr2:61842393 | C | T | 60 | a0001c0001t0002g0009 a0001c0001t0002g0112 a0001c0001t0002g0205 others(57): Show |
81 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.184-33G>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61842393 | |||||||
| chr2:61842564 | G | C | 1 | a0001c0001t0001g0085 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.184-204C>G | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61842564 | |||||||
| chr2:61842678 | T | C | 1 | a0003c0004t0003g0162 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.184-318A>G | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61842678 | |||||||
| chr2:61842728 | G | A | 1 | a0001c0001t0017g0117 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.184-368C>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61842728 | |||||||
| chr2:61842887 | C | T | 1 | a0003c0004t0003g0162 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.184-527G>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61842887 | |||||||
| chr2:61842929 | G | A | 1 | a0001c0003t0001g0136 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.184-569C>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61842929 | |||||||
| chr2:61843075 | G | A | 2 | a0001c0001t0001g0107 a0001c0001t0001g0108 |
2 | HG01243.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.184-715C>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61843075 | |||||||
| chr2:61843138 | TTTTG | T | 130 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(127): Show |
207 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.184-782_184-779del others(4): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61843138 | |||||||
| chr2:61843235 | C | G | 4 | a0001c0001t0002g0260 a0001c0001t0002g0265 a0001c0001t0002g0266 others(1): Show |
4 | HG02630.hp1 HG03098.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.184-875G>C | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61843235 | |||||||
| chr2:61843373 | C | T | 31 | a0001c0001t0002g0004 a0001c0001t0002g0016 a0001c0001t0002g0017 others(28): Show |
43 | HG01109.hp1 HG01167.hp2 HG01175.hp2 others(40): Show |
intron_variant | MODIFIER | c.184-1013G>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61843373 | |||||||
| chr2:61843417 | G | A | 2 | a0001c0001t0001g0036 a0001c0001t0001g0119 |
3 | HG00544.hp2 HG02040.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.184-1057C>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61843417 | |||||||
| chr2:61843425 | C | T | 6 | a0001c0001t0002g0016 a0001c0001t0002g0177 a0001c0001t0002g0178 others(3): Show |
8 | HG02055.hp2 HG02559.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.184-1065G>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61843425 | |||||||
| chr2:61843426 | C | A | 1 | a0005c0010t0018g0262 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.184-1066G>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61843426 | |||||||
| chr2:61843460 | A | C | 1 | a0001c0001t0017g0117 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.184-1100T>G | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61843460 | |||||||
| chr2:61843470 | A | C | 1 | a0002c0002t0002g0213 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.184-1110T>G | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61843470 | |||||||
| chr2:61843541 | T | C | 2 | a0002c0002t0002g0021 a0002c0002t0002g0238 |
4 | HG01192.hp2 HG01256.hp1 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.184-1181A>G | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61843541 | |||||||
| chr2:61843679 | A | C | 1 | a0001c0001t0002g0258 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.184-1319T>G | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61843679 | |||||||
| chr2:61843776 | T | G | 2 | a0001c0001t0002g0190 a0001c0001t0020g0191 |
2 | HG02886.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.184-1416A>C | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61843776 | |||||||
| chr2:61843898 | C | A | 2 | a0001c0001t0002g0174 a0001c0001t0002g0175 |
2 | HG03579.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.184-1538G>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61843898 | |||||||
| chr2:61843922 | T | A | 1 | a0001c0001t0016g0102 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.184-1562A>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61843922 | |||||||
| chr2:61844047 | G | A | 1 | a0009c0011t0002g0247 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.184-1687C>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61844047 | |||||||
| chr2:61844137 | T | C | 1 | a0001c0001t0017g0117 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.184-1777A>G | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61844137 | |||||||
| chr2:61844203 | T | C | 32 | a0001c0001t0002g0004 a0001c0001t0002g0016 a0001c0001t0002g0017 others(29): Show |
44 | HG01109.hp1 HG01167.hp2 HG01175.hp2 others(41): Show |
intron_variant | MODIFIER | c.184-1843A>G | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61844203 | |||||||
| chr2:61844349 | T | C | 126 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(123): Show |
200 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(197): Show |
intron_variant | MODIFIER | c.184-1989A>G | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61844349 | |||||||
| chr2:61844376 | G | C | 2 | a0002c0002t0002g0202 a0002c0002t0002g0213 |
2 | HG02683.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.184-2016C>G | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61844376 | |||||||
| chr2:61844383 | T | G | 268 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(265): Show |
395 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(392): Show |
intron_variant | MODIFIER | c.184-2023A>C | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61844383 | |||||||
| chr2:61844407 | C | T | 62 | a0001c0001t0002g0009 a0001c0001t0002g0112 a0001c0001t0002g0205 others(59): Show |
85 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(82): Show |
intron_variant | MODIFIER | c.184-2047G>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61844407 | |||||||
| chr2:61844427 | A | T | 65 | a0001c0001t0002g0009 a0001c0001t0002g0112 a0001c0001t0002g0174 others(62): Show |
88 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(85): Show |
intron_variant | MODIFIER | c.184-2067T>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61844427 | |||||||
| chr2:61844658 | C | T | 1 | a0001c0001t0004g0065 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.184-2298G>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61844658 | |||||||
| chr2:61844923 | C | T | 1 | a0011c0018t0015g0261 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.184-2563G>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61844923 | |||||||
| chr2:61844972 | G | C | 126 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(123): Show |
200 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(197): Show |
intron_variant | MODIFIER | c.184-2612C>G | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61844972 | |||||||
| chr2:61845039 | G | C | 1 | a0001c0001t0016g0102 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.184-2679C>G | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61845039 | |||||||
| chr2:61845148 | A | G | 268 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(265): Show |
395 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(392): Show |
intron_variant | MODIFIER | c.184-2788T>C | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61845148 | |||||||
| chr2:61845338 | G | A | 2 | a0001c0001t0001g0050 a0001c0001t0001g0259 |
3 | HG02280.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.184-2978C>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61845338 | |||||||
| chr2:61845341 | C | T | 1 | a0002c0002t0002g0227 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.184-2981G>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61845341 | |||||||
| chr2:61845342 | A | T | 131 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(128): Show |
208 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.184-2982T>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61845342 | |||||||
| chr2:61845371 | C | T | 1 | a0001c0001t0004g0062 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.184-3011G>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61845371 | |||||||
| chr2:61845670 | T | A | 87 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0010 others(84): Show |
126 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.184-3310A>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61845670 | |||||||
| chr2:61845744 | G | A | 11 | a0001c0001t0002g0260 a0001c0001t0002g0265 a0001c0001t0002g0266 others(8): Show |
13 | HG02280.hp1 HG02451.hp1 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.184-3384C>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61845744 | |||||||
| chr2:61845787 | C | T | 7 | a0001c0001t0004g0013 a0001c0001t0004g0058 a0001c0001t0004g0059 others(4): Show |
9 | HG00735.hp2 HG00741.hp2 HG01081.hp1 others(6): Show |
intron_variant | MODIFIER | c.184-3427G>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61845787 | |||||||
| chr2:61845816 | C | T | 1 | a0002c0002t0002g0204 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.184-3456G>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61845816 | |||||||
| chr2:61845925 | C | T | 14 | a0002c0002t0002g0019 a0002c0002t0002g0020 a0002c0002t0002g0044 others(11): Show |
19 | HG00323.hp2 HG00408.hp1 HG01943.hp1 others(16): Show |
intron_variant | MODIFIER | c.184-3565G>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61845925 | |||||||
| chr2:61846043 | C | T | 3 | a0001c0001t0002g0218 a0001c0001t0002g0220 a0001c0001t0002g0221 |
3 | HG00639.hp2 HG01255.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.184-3683G>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61846043 | |||||||
| chr2:61846064 | C | T | 1 | a0001c0001t0013g0148 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.184-3704G>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61846064 | |||||||
| chr2:61846088 | CA | C | 102 | a0001c0001t0001g0014 a0001c0001t0001g0086 a0001c0001t0001g0087 others(99): Show |
141 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(138): Show |
intron_variant | MODIFIER | c.184-3729delT | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61846088 | |||||||
| chr2:61846088 | CAA | C | 119 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(116): Show |
175 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.184-3730_184-3729d others(4): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61846088 | |||||||
| chr2:61846088 | CAAA | C | 34 | a0001c0001t0001g0060 a0001c0001t0002g0035 a0001c0001t0002g0132 others(31): Show |
65 | HG00140.hp2 HG00438.hp1 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.184-3731_184-3729d others(5): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61846088 | |||||||
| chr2:61846161 | A | T | 1 | a0001c0001t0002g0218 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.184-3801T>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61846161 | |||||||
| chr2:61846199 | G | A | 1 | a0001c0001t0001g0088 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.184-3839C>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61846199 | |||||||
| chr2:61846333 | G | A | 1 | a0001c0001t0024g0089 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.184-3973C>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61846333 | |||||||
| chr2:61846621 | C | G | 2 | a0001c0001t0010g0272 a0001c0001t0010g0273 |
2 | HG02922.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.184-4261G>C | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61846621 | |||||||
| chr2:61846627 | C | T | 1 | a0002c0002t0002g0217 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.184-4267G>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61846627 | |||||||
| chr2:61846688 | C | T | 4 | a0001c0001t0001g0036 a0001c0001t0001g0105 a0001c0001t0001g0113 others(1): Show |
5 | HG00544.hp2 HG02040.hp1 HG02165.hp1 others(2): Show |
intron_variant | MODIFIER | c.184-4328G>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61846688 | |||||||
| chr2:61846783 | C | T | 136 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0002g0004 others(133): Show |
186 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.184-4423G>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61846783 | |||||||
| chr2:61846882 | G | C | 24 | a0001c0001t0001g0008 a0001c0001t0001g0030 a0001c0001t0001g0036 others(21): Show |
33 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(30): Show |
intron_variant | MODIFIER | c.184-4522C>G | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61846882 | |||||||
| chr2:61846962 | G | A | 56 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0022 others(53): Show |
86 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.184-4602C>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61846962 | |||||||
| chr2:61847005 | A | AAC | 268 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(265): Show |
395 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(392): Show |
intron_variant | MODIFIER | c.184-4647_184-4646d others(4): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61847005 | |||||||
| chr2:61847019 | G | A | 26 | a0003c0004t0003g0003 a0003c0004t0003g0015 a0003c0004t0003g0031 others(23): Show |
39 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(36): Show |
intron_variant | MODIFIER | c.184-4659C>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61847019 | |||||||
| chr2:61847054 | C | T | 2 | a0001c0001t0001g0090 a0001c0001t0001g0091 |
2 | NA19064.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.184-4694G>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61847054 | |||||||
| chr2:61847424 | C | G | 1 | a0001c0001t0001g0113 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.184-5064G>C | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61847424 | |||||||
| chr2:61847424 | C | T | 125 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(122): Show |
199 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.184-5064G>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61847424 | |||||||
| chr2:61847589 | G | T | 1 | a0001c0001t0002g0260 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.184-5229C>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61847589 | |||||||
| chr2:61847702 | G | A | 125 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(122): Show |
199 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.184-5342C>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61847702 | |||||||
| chr2:61847716 | G | A | 2 | a0001c0001t0001g0090 a0001c0001t0001g0091 |
2 | NA19064.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.184-5356C>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61847716 | |||||||
| chr2:61847797 | G | A | 125 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(122): Show |
199 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.184-5437C>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61847797 | |||||||
| chr2:61847983 | T | C | 1 | a0003c0004t0003g0171 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.184-5623A>G | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61847983 | |||||||
| chr2:61847988 | T | G | 26 | a0003c0004t0003g0003 a0003c0004t0003g0015 a0003c0004t0003g0031 others(23): Show |
39 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(36): Show |
intron_variant | MODIFIER | c.184-5628A>C | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61847988 | |||||||
| chr2:61848241 | G | C | 1 | a0001c0001t0001g0108 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.183+5618C>G | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848241 | |||||||
| chr2:61848320 | A | G | 2 | a0002c0002t0002g0043 a0002c0002t0002g0254 |
3 | HG02647.hp2 HG02723.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.183+5539T>C | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848320 | |||||||
| chr2:61848597 | T | C | 268 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(265): Show |
395 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(392): Show |
intron_variant | MODIFIER | c.183+5262A>G | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848597 | |||||||
| chr2:61848814 | T | G | 1 | a0001c0001t0017g0117 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.183+5045A>C | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848814 | |||||||
| chr2:61848814 | TTA | T | 60 | a0001c0001t0001g0113 a0001c0001t0002g0009 a0001c0001t0002g0112 others(57): Show |
83 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.183+5043_183+5044d others(4): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848814 | |||||||
| chr2:61848816 | ATATATAT others(5): Show |
A | 1 | a0002c0002t0019g0214 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.183+5031_183+5042d others(14): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848816 | |||||||
| chr2:61848816 | ATATATAT others(15): Show |
A | 3 | a0004c0005t0002g0249 a0004c0005t0005g0048 a0004c0005t0005g0250 |
4 | HG02451.hp1 HG03041.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.183+5021_183+5042d others(24): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848816 | |||||||
| chr2:61848818 | ATATATAT others(3): Show |
A | 5 | a0001c0001t0002g0260 a0001c0001t0002g0265 a0005c0010t0018g0262 others(2): Show |
5 | HG02622.hp1 HG02965.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.183+5031_183+5040d others(12): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848818 | |||||||
| chr2:61848818 | ATATATAT others(115): Show |
A | 2 | a0005c0007t0009g0263 a0005c0007t0009g0264 |
2 | HG02572.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.183+4919_183+5040d others(2): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848818 | |||||||
| chr2:61848824 | A | ATATTTAT others(9): Show |
1 | a0003c0004t0003g0167 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.183+5034_183+5035i others(18): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848824 | |||||||
| chr2:61848824 | A | T | 129 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(126): Show |
205 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(202): Show |
intron_variant | MODIFIER | c.183+5035T>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848824 | |||||||
| chr2:61848824 | ATATCTAT others(19): Show |
A | 1 | a0002c0002t0002g0238 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.183+5009_183+5034d others(28): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848824 | |||||||
| chr2:61848826 | A | T | 1 | a0004c0005t0005g0049 | 2 | HG02280.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.183+5033T>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848826 | |||||||
| chr2:61848826 | ATC | A | 124 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(121): Show |
197 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.183+5031_183+5032d others(4): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848826 | |||||||
| chr2:61848828 | C | A | 8 | a0001c0001t0001g0014 a0001c0001t0001g0050 a0001c0001t0001g0097 others(5): Show |
12 | HG01891.hp1 HG02145.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.183+5031G>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848828 | |||||||
| chr2:61848828 | C | T | 125 | a0001c0001t0001g0006 a0001c0001t0001g0107 a0001c0001t0001g0108 others(122): Show |
173 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.183+5031G>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848828 | |||||||
| chr2:61848828 | CTATATAT others(17): Show |
C | 3 | a0001c0006t0002g0268 a0001c0006t0002g0269 a0001c0006t0002g0271 |
3 | HG00280.hp2 HG01261.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.183+5007_183+5030d others(26): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848828 | |||||||
| chr2:61848830 | A | G | 1 | a0001c0001t0001g0056 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.183+5029T>C | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848830 | |||||||
| chr2:61848833 | T | A | 1 | a0001c0001t0002g0265 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.183+5026A>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848833 | |||||||
| chr2:61848834 | ATATTTAT others(137): Show |
A | 1 | a0001c0001t0002g0266 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.183+4881_183+5024d others(2): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848834 | |||||||
| chr2:61848836 | A | ATATT | 25 | a0003c0004t0003g0003 a0003c0004t0003g0015 a0003c0004t0003g0031 others(22): Show |
38 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(35): Show |
intron_variant | MODIFIER | c.183+5022_183+5023i others(6): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848836 | |||||||
| chr2:61848836 | A | T | 5 | a0001c0001t0001g0014 a0001c0001t0001g0050 a0001c0001t0001g0103 others(2): Show |
8 | HG01891.hp1 HG02145.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.183+5023T>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848836 | |||||||
| chr2:61848838 | T | A | 32 | a0001c0001t0001g0014 a0001c0001t0001g0050 a0001c0001t0001g0103 others(29): Show |
48 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(45): Show |
intron_variant | MODIFIER | c.183+5021A>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848838 | |||||||
| chr2:61848840 | A | T | 2 | a0001c0001t0001g0107 a0001c0001t0001g0108 |
2 | HG01243.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.183+5019T>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848840 | |||||||
| chr2:61848850 | T | A | 1 | a0001c0001t0001g0108 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.183+5009A>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848850 | |||||||
| chr2:61848850 | TTA | T | 18 | a0001c0001t0001g0120 a0002c0002t0002g0007 a0002c0002t0002g0018 others(15): Show |
27 | HG00099.hp1 HG01169.hp1 HG01256.hp2 others(24): Show |
intron_variant | MODIFIER | c.183+5007_183+5008d others(4): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848850 | |||||||
| chr2:61848850 | TTATATAT others(131): Show |
T | 1 | a0001c0001t0001g0001 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.183+4871_183+5008d others(2): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848850 | |||||||
| chr2:61848852 | A | ATATATAT others(3): Show |
7 | a0001c0001t0002g0017 a0001c0001t0002g0177 a0001c0001t0002g0186 others(4): Show |
8 | HG01070.hp2 HG01891.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.183+4997_183+5006d others(12): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848852 | |||||||
| chr2:61848852 | A | T | 3 | a0001c0001t0001g0108 a0002c0002t0002g0238 a0003c0004t0003g0003 |
3 | HG01192.hp2 HG01243.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.183+5007T>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848852 | |||||||
| chr2:61848852 | ATATATAT others(3): Show |
A | 1 | a0001c0001t0017g0117 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.183+4997_183+5006d others(12): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848852 | |||||||
| chr2:61848862 | T | TTA | 3 | a0003c0004t0003g0118 a0003c0004t0003g0170 a0003c0004t0003g0171 |
3 | HG00140.hp1 HG00280.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.183+4995_183+4996d others(4): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848862 | |||||||
| chr2:61848862 | TTA | T | 54 | a0001c0001t0001g0113 a0001c0001t0002g0004 a0001c0001t0002g0009 others(51): Show |
68 | HG00323.hp2 HG00408.hp1 HG00639.hp2 others(65): Show |
intron_variant | MODIFIER | c.183+4995_183+4996d others(4): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848862 | |||||||
| chr2:61848862 | TTATA | T | 121 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(118): Show |
193 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.183+4993_183+4996d others(6): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848862 | |||||||
| chr2:61848862 | TTATATAT others(119): Show |
T | 1 | a0001c0001t0001g0006 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.183+4871_183+4996d others(2): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848862 | |||||||
| chr2:61848864 | A | ATATATAT others(95): Show |
1 | a0003c0004t0003g0172 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.183+4994_183+4995i others(104): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848864 | |||||||
| chr2:61848864 | A | ATATATAT others(117): Show |
1 | a0003c0004t0003g0039 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.183+4994_183+4995i others(126): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848864 | |||||||
| chr2:61848864 | A | ATATATAT others(71): Show |
1 | a0003c0004t0003g0003 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.183+4994_183+4995i others(80): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848864 | |||||||
| chr2:61848864 | A | ATATATAT others(95): Show |
1 | a0003c0004t0003g0160 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.183+4994_183+4995i others(104): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848864 | |||||||
| chr2:61848864 | A | ATATATAT others(47): Show |
2 | a0003c0004t0003g0039 a0003c0004t0003g0166 |
2 | HG00642.hp1 HG01109.hp2 |
intron_variant | MODIFIER | c.183+4994_183+4995i others(56): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848864 | |||||||
| chr2:61848864 | A | ATATATAT others(69): Show |
14 | a0003c0004t0003g0003 a0003c0004t0003g0015 a0003c0004t0003g0031 others(11): Show |
21 | HG00423.hp2 HG00597.hp2 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.183+4994_183+4995i others(78): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848864 | |||||||
| chr2:61848864 | A | ATATATAT others(91): Show |
5 | a0003c0004t0003g0003 a0003c0004t0003g0047 a0003c0004t0003g0109 others(2): Show |
6 | HG01123.hp2 HG01361.hp1 HG01981.hp2 others(3): Show |
intron_variant | MODIFIER | c.183+4994_183+4995i others(100): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848864 | |||||||
| chr2:61848866 | A | ATATATAA others(17): Show |
1 | a0001c0001t0002g0004 | 3 | HG01109.hp1 HG01884.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.183+4992_183+4993i others(26): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848866 | |||||||
| chr2:61848866 | A | ATATATTT others(15): Show |
17 | a0001c0001t0002g0004 a0001c0001t0002g0016 a0001c0001t0002g0017 others(14): Show |
23 | HG01257.hp2 HG01258.hp1 HG01496.hp1 others(20): Show |
intron_variant | MODIFIER | c.183+4992_183+4993i others(24): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848866 | |||||||
| chr2:61848866 | A | T | 5 | a0001c0001t0002g0110 a0001c0001t0002g0192 a0001c0001t0002g0193 others(2): Show |
5 | NA18939.hp2 NA18985.hp2 NA18992.hp2 others(2): Show |
intron_variant | MODIFIER | c.183+4993T>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848866 | |||||||
| chr2:61848870 | A | T | 6 | a0001c0001t0001g0030 a0001c0001t0001g0101 a0001c0001t0001g0149 others(3): Show |
7 | HG01192.hp1 NA18946.hp1 NA18947.hp2 others(4): Show |
intron_variant | MODIFIER | c.183+4989T>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848870 | |||||||
| chr2:61848872 | ATT | A | 3 | a0001c0001t0001g0149 a0001c0001t0001g0157 a0001c0001t0001g0245 |
3 | NA18946.hp1 NA18985.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.183+4985_183+4986d others(4): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848872 | |||||||
| chr2:61848872 | ATTTATAT others(137): Show |
A | 2 | a0001c0001t0001g0030 a0001c0001t0001g0101 |
3 | NA18947.hp2 NA19064.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.183+4843_183+4986d others(2): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848872 | |||||||
| chr2:61848874 | T | A | 1 | a0001c0003t0001g0125 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.183+4985A>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848874 | |||||||
| chr2:61848874 | TTATA | T | 4 | a0001c0001t0002g0260 a0001c0001t0002g0265 a0004c0005t0005g0049 others(1): Show |
5 | HG02280.hp1 HG03098.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.183+4981_183+4984d others(6): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848874 | |||||||
| chr2:61848876 | ATATATAT others(3): Show |
A | 1 | a0001c0001t0016g0102 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.183+4973_183+4982d others(12): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848876 | |||||||
| chr2:61848876 | ATATATAT others(133): Show |
A | 2 | a0001c0001t0001g0120 a0005c0010t0018g0262 |
2 | HG02622.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.183+4843_183+4982d others(2): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848876 | |||||||
| chr2:61848878 | A | T | 7 | a0001c0001t0002g0017 a0001c0001t0002g0177 a0001c0001t0002g0186 others(4): Show |
8 | HG01167.hp2 HG01891.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.183+4981T>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848878 | |||||||
| chr2:61848881 | TATATTTA others(181): Show |
T | 1 | a0001c0001t0004g0013 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.183+4790_183+4977d others(2): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848881 | |||||||
| chr2:61848882 | A | T | 2 | a0001c0003t0001g0012 a0001c0003t0001g0125 |
2 | HG01192.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.183+4977T>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848882 | |||||||
| chr2:61848883 | TATTTATA others(179): Show |
T | 1 | a0001c0003t0001g0012 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.183+4790_183+4975d others(2): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848883 | |||||||
| chr2:61848884 | A | T | 26 | a0001c0001t0001g0107 a0001c0001t0002g0004 a0001c0001t0002g0016 others(23): Show |
36 | HG01109.hp1 HG01257.hp2 HG01258.hp1 others(33): Show |
intron_variant | MODIFIER | c.183+4975T>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848884 | |||||||
| chr2:61848886 | T | A | 27 | a0001c0001t0001g0107 a0001c0001t0002g0004 a0001c0001t0002g0016 others(24): Show |
37 | HG01109.hp1 HG01192.hp1 HG01257.hp2 others(34): Show |
intron_variant | MODIFIER | c.183+4973A>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848886 | |||||||
| chr2:61848886 | T | TTATATAT others(5): Show |
1 | a0001c0001t0002g0199 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.183+4961_183+4972d others(14): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848886 | |||||||
| chr2:61848886 | TTA | T | 6 | a0001c0001t0001g0014 a0001c0001t0001g0050 a0001c0001t0001g0103 others(3): Show |
9 | HG01891.hp1 HG02132.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.183+4971_183+4972d others(4): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848886 | |||||||
| chr2:61848886 | TTATATAT others(35): Show |
T | 17 | a0001c0001t0001g0113 a0001c0001t0002g0009 a0001c0001t0002g0218 others(14): Show |
23 | HG00639.hp2 HG01255.hp2 HG02074.hp2 others(20): Show |
intron_variant | MODIFIER | c.183+4931_183+4972d others(44): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848886 | |||||||
| chr2:61848886 | TTATATAT others(75): Show |
T | 3 | a0001c0001t0002g0174 a0001c0001t0002g0175 a0001c0001t0002g0258 |
3 | HG03579.hp1 HG03579.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.183+4891_183+4972d others(84): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848886 | |||||||
| chr2:61848888 | ATATATAT others(185): Show |
A | 1 | a0001c0003t0001g0005 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.183+4779_183+4970d others(2): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848888 | |||||||
| chr2:61848889 | TATATATT others(173): Show |
T | 29 | a0001c0001t0002g0035 a0001c0001t0002g0132 a0001c0001t0002g0134 others(26): Show |
56 | HG00438.hp1 HG00558.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.183+4790_183+4969d others(2): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848889 | |||||||
| chr2:61848890 | A | T | 4 | a0001c0001t0002g0179 a0001c0001t0002g0197 a0001c0001t0002g0198 others(1): Show |
4 | HG01175.hp2 HG02602.hp2 NA18955.hp1 others(1): Show |
intron_variant | MODIFIER | c.183+4969T>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848890 | |||||||
| chr2:61848890 | ATATATTT others(11): Show |
A | 2 | a0002c0002t0002g0021 a0002c0002t0002g0237 |
4 | HG00738.hp2 HG01256.hp1 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.183+4951_183+4968d others(20): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848890 | |||||||
| chr2:61848890 | ATATATTT others(81): Show |
A | 1 | a0002c0002t0002g0224 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.183+4881_183+4968d others(90): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848890 | |||||||
| chr2:61848893 | TATTTATA others(169): Show |
T | 89 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(86): Show |
130 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.183+4790_183+4965d others(2): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848893 | |||||||
| chr2:61848896 | T | A | 25 | a0001c0001t0002g0179 a0001c0001t0002g0197 a0001c0001t0002g0198 others(22): Show |
32 | HG00323.hp2 HG00408.hp1 HG01175.hp2 others(29): Show |
intron_variant | MODIFIER | c.183+4963A>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848896 | |||||||
| chr2:61848898 | A | T | 25 | a0001c0001t0002g0179 a0001c0001t0002g0197 a0001c0001t0002g0198 others(22): Show |
32 | HG00323.hp2 HG00408.hp1 HG01175.hp2 others(29): Show |
intron_variant | MODIFIER | c.183+4961T>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848898 | |||||||
| chr2:61848898 | ATATATAT others(111): Show |
A | 1 | a0004c0005t0005g0049 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.183+4843_183+4960d others(2): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848898 | |||||||
| chr2:61848902 | ATATATTT others(170): Show |
A | 1 | a0001c0001t0001g0097 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.183+4780_183+4956d others(2): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848902 | |||||||
| chr2:61848904 | A | T | 1 | a0001c0001t0001g0107 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.183+4955T>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848904 | |||||||
| chr2:61848908 | T | A | 1 | a0001c0001t0002g0004 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.183+4951A>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848908 | |||||||
| chr2:61848908 | T | TTA | 21 | a0003c0004t0003g0003 a0003c0004t0003g0015 a0003c0004t0003g0031 others(18): Show |
33 | HG00423.hp2 HG00597.hp2 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.183+4949_183+4950d others(4): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848908 | |||||||
| chr2:61848908 | T | TTATATAT others(107): Show |
1 | a0003c0004t0003g0170 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.183+4950_183+4951i others(116): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848908 | |||||||
| chr2:61848908 | T | TTATATAT others(93): Show |
1 | a0003c0004t0003g0171 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.183+4950_183+4951i others(102): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848908 | |||||||
| chr2:61848908 | T | TTATATAT others(61): Show |
1 | a0003c0004t0003g0167 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.183+4950_183+4951i others(70): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848908 | |||||||
| chr2:61848908 | T | TTATATAT others(95): Show |
1 | a0003c0004t0003g0015 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.183+4950_183+4951i others(104): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848908 | |||||||
| chr2:61848908 | T | TTATATAT others(117): Show |
1 | a0003c0004t0003g0161 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.183+4950_183+4951i others(126): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848908 | |||||||
| chr2:61848910 | ATATATT | A | 3 | a0002c0002t0002g0210 a0002c0002t0002g0211 a0002c0002t0002g0238 |
3 | HG01192.hp2 NA19004.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.183+4943_183+4948d others(8): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848910 | |||||||
| chr2:61848911 | TATATTTA others(151): Show |
T | 2 | a0001c0003t0001g0125 a0001c0003t0001g0158 |
2 | HG01192.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.183+4790_183+4947d others(2): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848911 | |||||||
| chr2:61848911 | TATATTTA others(177): Show |
T | 1 | a0001c0001t0024g0089 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.183+4764_183+4947d others(2): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848911 | |||||||
| chr2:61848912 | ATATTTAT others(59): Show |
A | 17 | a0002c0002t0002g0019 a0002c0002t0002g0020 a0002c0002t0002g0044 others(14): Show |
22 | HG00323.hp2 HG00408.hp1 HG01943.hp1 others(19): Show |
intron_variant | MODIFIER | c.183+4881_183+4946d others(68): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848912 | |||||||
| chr2:61848912 | ATATTTAT others(137): Show |
A | 1 | a0004c0005t0005g0049 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.183+4803_183+4946d others(2): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848912 | |||||||
| chr2:61848916 | T | A | 28 | a0001c0001t0002g0017 a0001c0001t0002g0112 a0001c0001t0002g0179 others(25): Show |
36 | HG00099.hp1 HG00140.hp1 HG01169.hp1 others(33): Show |
intron_variant | MODIFIER | c.183+4943A>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848916 | |||||||
| chr2:61848918 | A | ATT | 3 | a0001c0001t0002g0017 a0001c0001t0002g0200 a0003c0004t0003g0118 |
4 | HG00140.hp1 HG03688.hp1 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.183+4940_183+4941i others(4): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848918 | |||||||
| chr2:61848918 | A | T | 20 | a0001c0001t0002g0112 a0001c0001t0002g0205 a0001c0001t0002g0206 others(17): Show |
27 | HG00099.hp1 HG01169.hp1 HG01346.hp1 others(24): Show |
intron_variant | MODIFIER | c.183+4941T>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848918 | |||||||
| chr2:61848918 | ATATATAT others(83): Show |
A | 1 | a0001c0001t0001g0108 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.183+4851_183+4940d others(92): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848918 | |||||||
| chr2:61848920 | A | T | 5 | a0001c0001t0002g0179 a0001c0001t0002g0197 a0001c0001t0002g0198 others(2): Show |
5 | HG01175.hp2 HG02602.hp2 NA18955.hp1 others(2): Show |
intron_variant | MODIFIER | c.183+4939T>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848920 | |||||||
| chr2:61848925 | TTTATATA others(137): Show |
T | 1 | a0001c0001t0002g0260 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.183+4790_183+4933d others(2): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848925 | |||||||
| chr2:61848926 | T | A | 31 | a0001c0001t0002g0179 a0001c0001t0002g0197 a0001c0001t0002g0198 others(28): Show |
44 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(41): Show |
intron_variant | MODIFIER | c.183+4933A>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848926 | |||||||
| chr2:61848926 | TTA | T | 4 | a0001c0001t0002g0009 a0002c0002t0002g0021 a0002c0002t0002g0210 others(1): Show |
6 | HG00738.hp2 HG01256.hp1 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.183+4931_183+4932d others(4): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848926 | |||||||
| chr2:61848926 | TTATATAT others(33): Show |
T | 1 | a0001c0001t0017g0117 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.183+4893_183+4932d others(42): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848926 | |||||||
| chr2:61848926 | TTATATAT others(149): Show |
T | 2 | a0001c0001t0001g0103 a0001c0001t0001g0111 |
2 | HG01891.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.183+4777_183+4932d others(2): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848926 | |||||||
| chr2:61848927 | TATATATA others(161): Show |
T | 1 | a0009c0011t0002g0247 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.183+4764_183+4931d others(2): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848927 | |||||||
| chr2:61848928 | A | T | 26 | a0003c0004t0003g0003 a0003c0004t0003g0015 a0003c0004t0003g0031 others(23): Show |
39 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(36): Show |
intron_variant | MODIFIER | c.183+4931T>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848928 | |||||||
| chr2:61848928 | ATATATAT others(5): Show |
A | 1 | a0002c0002t0002g0018 | 3 | HG01256.hp2 HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.183+4919_183+4930d others(14): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848928 | |||||||
| chr2:61848928 | ATATATAT others(81): Show |
A | 3 | a0004c0005t0002g0249 a0004c0005t0005g0048 a0004c0005t0005g0250 |
4 | HG02451.hp1 HG03041.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.183+4843_183+4930d others(90): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848928 | |||||||
| chr2:61848929 | TATATATA others(159): Show |
T | 1 | a0001c0001t0001g0014 | 3 | HG02145.hp2 HG02630.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.183+4764_183+4929d others(2): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848929 | |||||||
| chr2:61848930 | A | T | 1 | a0002c0002t0002g0231 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.183+4929T>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848930 | |||||||
| chr2:61848932 | A | T | 6 | a0001c0001t0001g0107 a0001c0001t0002g0179 a0001c0001t0002g0197 others(3): Show |
6 | HG01175.hp2 HG02602.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.183+4927T>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848932 | |||||||
| chr2:61848934 | ATATATTT others(151): Show |
A | 1 | a0001c0001t0002g0265 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.183+4767_183+4924d others(2): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848934 | |||||||
| chr2:61848936 | A | T | 24 | a0001c0001t0002g0017 a0001c0001t0002g0112 a0001c0001t0002g0200 others(21): Show |
32 | HG00099.hp1 HG01169.hp1 HG01192.hp2 others(29): Show |
intron_variant | MODIFIER | c.183+4923T>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848936 | |||||||
| chr2:61848938 | A | T | 29 | a0001c0001t0001g0050 a0001c0001t0001g0259 a0001c0001t0002g0004 others(26): Show |
40 | HG01109.hp1 HG01167.hp2 HG01257.hp2 others(37): Show |
intron_variant | MODIFIER | c.183+4921T>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848938 | |||||||
| chr2:61848938 | ATT | A | 21 | a0001c0001t0002g0112 a0001c0001t0002g0205 a0001c0001t0002g0206 others(18): Show |
28 | HG00099.hp1 HG01169.hp1 HG01192.hp2 others(25): Show |
intron_variant | MODIFIER | c.183+4919_183+4920d others(4): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848938 | |||||||
| chr2:61848939 | TTTATATA others(149): Show |
T | 2 | a0001c0001t0001g0050 a0001c0001t0001g0259 |
3 | HG02280.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.183+4764_183+4919d others(2): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848939 | |||||||
| chr2:61848940 | T | A | 29 | a0001c0001t0002g0004 a0001c0001t0002g0016 a0001c0001t0002g0017 others(26): Show |
41 | HG01109.hp1 HG01167.hp2 HG01257.hp2 others(38): Show |
intron_variant | MODIFIER | c.183+4919A>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848940 | |||||||
| chr2:61848942 | A | T | 2 | a0001c0001t0016g0102 a0003c0004t0003g0015 |
2 | HG00741.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.183+4917T>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848942 | |||||||
| chr2:61848948 | A | T | 3 | a0001c0001t0002g0017 a0001c0001t0002g0200 a0002c0002t0002g0211 |
4 | HG03688.hp1 HG03704.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.183+4911T>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848948 | |||||||
| chr2:61848950 | T | A | 3 | a0001c0001t0002g0017 a0001c0001t0002g0200 a0002c0002t0002g0211 |
4 | HG03688.hp1 HG03704.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.183+4909A>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848950 | |||||||
| chr2:61848954 | A | ATATATT | 5 | a0001c0001t0002g0110 a0001c0001t0002g0192 a0001c0001t0002g0193 others(2): Show |
5 | NA18939.hp2 NA18985.hp2 NA18992.hp2 others(2): Show |
intron_variant | MODIFIER | c.183+4904_183+4905i others(8): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848954 | |||||||
| chr2:61848956 | A | ATT | 20 | a0001c0001t0002g0004 a0001c0001t0002g0016 a0001c0001t0002g0177 others(17): Show |
30 | HG01109.hp1 HG01167.hp2 HG01257.hp2 others(27): Show |
intron_variant | MODIFIER | c.183+4902_183+4903i others(4): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848956 | |||||||
| chr2:61848956 | A | T | 2 | a0001c0001t0002g0017 a0001c0001t0002g0200 |
3 | HG03688.hp1 HG03704.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.183+4903T>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848956 | |||||||
| chr2:61848957 | TATATTTA others(105): Show |
T | 1 | a0002c0002t0002g0231 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.183+4790_183+4901d others(2): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848957 | |||||||
| chr2:61848958 | A | T | 23 | a0001c0001t0002g0017 a0001c0001t0002g0112 a0001c0001t0002g0205 others(20): Show |
32 | HG00099.hp1 HG01169.hp1 HG01256.hp2 others(29): Show |
intron_variant | MODIFIER | c.183+4901T>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848958 | |||||||
| chr2:61848958 | ATATTTAT others(127): Show |
A | 1 | a0011c0018t0015g0261 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.183+4767_183+4900d others(2): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848958 | |||||||
| chr2:61848962 | T | A | 49 | a0001c0001t0002g0004 a0001c0001t0002g0016 a0001c0001t0002g0017 others(46): Show |
70 | HG00099.hp1 HG01109.hp1 HG01167.hp2 others(67): Show |
intron_variant | MODIFIER | c.183+4897A>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848962 | |||||||
| chr2:61848962 | TTATATA | T | 18 | a0001c0001t0001g0113 a0001c0001t0002g0009 a0001c0001t0002g0218 others(15): Show |
27 | HG00639.hp2 HG00738.hp2 HG01192.hp2 others(24): Show |
intron_variant | MODIFIER | c.183+4891_183+4896d others(8): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848962 | |||||||
| chr2:61848966 | A | ATATATTT others(89): Show |
1 | a0003c0004t0003g0118 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.183+4892_183+4893i others(98): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848966 | |||||||
| chr2:61848966 | A | T | 28 | a0001c0001t0002g0004 a0001c0001t0002g0016 a0001c0001t0002g0017 others(25): Show |
39 | HG01109.hp1 HG01167.hp2 HG01257.hp2 others(36): Show |
intron_variant | MODIFIER | c.183+4893T>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848966 | |||||||
| chr2:61848968 | A | ATATATT | 23 | a0003c0004t0003g0003 a0003c0004t0003g0015 a0003c0004t0003g0031 others(20): Show |
36 | HG00280.hp1 HG00423.hp2 HG00597.hp2 others(33): Show |
intron_variant | MODIFIER | c.183+4890_183+4891i others(8): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848968 | |||||||
| chr2:61848968 | A | T | 23 | a0001c0001t0002g0017 a0001c0001t0002g0112 a0001c0001t0002g0205 others(20): Show |
32 | HG00099.hp1 HG01169.hp1 HG01256.hp2 others(29): Show |
intron_variant | MODIFIER | c.183+4891T>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848968 | |||||||
| chr2:61848972 | A | T | 1 | a0003c0004t0003g0160 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.183+4887T>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848972 | |||||||
| chr2:61848974 | A | T | 7 | a0001c0001t0002g0197 a0001c0001t0002g0198 a0005c0007t0009g0263 others(4): Show |
7 | HG02572.hp1 HG02602.hp2 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.183+4885T>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848974 | |||||||
| chr2:61848976 | ATT | A | 3 | a0003c0004t0003g0160 a0006c0008t0002g0215 a0006c0008t0002g0216 |
3 | HG02965.hp2 HG03704.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.183+4881_183+4882d others(4): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848976 | |||||||
| chr2:61848978 | T | A | 5 | a0001c0001t0002g0197 a0001c0001t0002g0198 a0005c0007t0009g0263 others(2): Show |
5 | HG02572.hp1 HG02602.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.183+4881A>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848978 | |||||||
| chr2:61848984 | A | T | 6 | a0001c0001t0002g0197 a0001c0001t0002g0198 a0001c0001t0002g0266 others(3): Show |
6 | HG02572.hp1 HG02602.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.183+4875T>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848984 | |||||||
| chr2:61848986 | T | A | 32 | a0001c0001t0002g0179 a0001c0001t0002g0197 a0001c0001t0002g0198 others(29): Show |
45 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(42): Show |
intron_variant | MODIFIER | c.183+4873A>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848986 | |||||||
| chr2:61848988 | A | T | 25 | a0003c0004t0003g0003 a0003c0004t0003g0015 a0003c0004t0003g0031 others(22): Show |
38 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(35): Show |
intron_variant | MODIFIER | c.183+4871T>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848988 | |||||||
| chr2:61848990 | A | T | 1 | a0001c0001t0002g0179 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.183+4869T>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848990 | |||||||
| chr2:61848996 | T | A | 4 | a0001c0001t0002g0179 a0003c0004t0003g0160 a0006c0008t0002g0215 others(1): Show |
4 | HG01175.hp2 HG02965.hp2 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.183+4863A>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848996 | |||||||
| chr2:61848996 | TTA | T | 24 | a0001c0001t0002g0004 a0001c0001t0002g0016 a0001c0001t0002g0017 others(21): Show |
36 | HG01109.hp1 HG01167.hp2 HG01257.hp2 others(33): Show |
intron_variant | MODIFIER | c.183+4861_183+4862d others(4): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848996 | |||||||
| chr2:61848998 | A | T | 4 | a0001c0001t0002g0179 a0003c0004t0003g0160 a0006c0008t0002g0215 others(1): Show |
4 | HG01175.hp2 HG02965.hp2 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.183+4861T>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848998 | |||||||
| chr2:61849006 | A | T | 3 | a0001c0001t0001g0107 a0001c0001t0002g0177 a0001c0001t0002g0178 |
3 | HG02055.hp2 HG02559.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.183+4853T>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61849006 | |||||||
| chr2:61849008 | T | A | 1 | a0001c0001t0001g0107 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.183+4851A>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61849008 | |||||||
| chr2:61849008 | TTATATAT others(83): Show |
T | 23 | a0001c0001t0002g0112 a0001c0001t0002g0205 a0001c0001t0002g0206 others(20): Show |
32 | HG00099.hp1 HG01169.hp1 HG01256.hp2 others(29): Show |
intron_variant | MODIFIER | c.183+4761_183+4850d others(92): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61849008 | |||||||
| chr2:61849010 | A | ATATATTT others(21): Show |
1 | a0001c0001t0002g0110 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.183+4848_183+4849i others(30): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61849010 | |||||||
| chr2:61849010 | A | T | 24 | a0001c0001t0002g0004 a0001c0001t0002g0016 a0001c0001t0002g0017 others(21): Show |
36 | HG01109.hp1 HG01167.hp2 HG01175.hp2 others(33): Show |
intron_variant | MODIFIER | c.183+4849T>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61849010 | |||||||
| chr2:61849016 | T | A | 2 | a0002c0002t0002g0224 a0003c0004t0003g0160 |
2 | HG02965.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.183+4843A>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61849016 | |||||||
| chr2:61849018 | A | T | 2 | a0002c0002t0002g0224 a0003c0004t0003g0160 |
2 | HG02965.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.183+4841T>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61849018 | |||||||
| chr2:61849026 | T | A | 2 | a0001c0001t0001g0107 a0002c0002t0002g0224 |
2 | NA19030.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.183+4833A>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61849026 | |||||||
| chr2:61849026 | TTA | T | 41 | a0001c0001t0001g0113 a0001c0001t0002g0009 a0001c0001t0002g0192 others(38): Show |
55 | HG00323.hp2 HG00408.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.183+4831_183+4832d others(4): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61849026 | |||||||
| chr2:61849028 | A | T | 1 | a0001c0001t0002g0258 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.183+4831T>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61849028 | |||||||
| chr2:61849030 | A | T | 1 | a0002c0002t0002g0224 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.183+4829T>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61849030 | |||||||
| chr2:61849036 | A | T | 24 | a0001c0001t0002g0004 a0001c0001t0002g0016 a0001c0001t0002g0017 others(21): Show |
36 | HG01109.hp1 HG01167.hp2 HG01175.hp2 others(33): Show |
intron_variant | MODIFIER | c.183+4823T>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61849036 | |||||||
| chr2:61849040 | A | T | 4 | a0001c0001t0002g0192 a0001c0001t0002g0193 a0001c0001t0002g0194 others(1): Show |
4 | NA18939.hp2 NA18985.hp2 NA18992.hp2 others(1): Show |
intron_variant | MODIFIER | c.183+4819T>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61849040 | |||||||
| chr2:61849041 | T | G | 1 | a0006c0008t0002g0215 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.183+4818A>C | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61849041 | |||||||
| chr2:61849046 | T | A | 1 | a0001c0001t0001g0107 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.183+4813A>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61849046 | |||||||
| chr2:61849052 | A | ATT | 4 | a0001c0001t0002g0017 a0001c0001t0002g0179 a0001c0001t0002g0200 others(1): Show |
5 | HG01175.hp2 HG02965.hp2 HG03688.hp1 others(2): Show |
intron_variant | MODIFIER | c.183+4806_183+4807i others(4): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61849052 | |||||||
| chr2:61849052 | ATATT | A | 7 | a0001c0001t0001g0030 a0001c0001t0001g0101 a0001c0001t0001g0120 others(4): Show |
9 | HG02280.hp1 HG02451.hp1 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.183+4803_183+4806d others(6): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61849052 | |||||||
| chr2:61849056 | T | A | 4 | a0001c0001t0002g0017 a0001c0001t0002g0179 a0001c0001t0002g0200 others(1): Show |
5 | HG01175.hp2 HG02965.hp2 HG03688.hp1 others(2): Show |
intron_variant | MODIFIER | c.183+4803A>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61849056 | |||||||
| chr2:61849056 | TTATATAT others(7): Show |
T | 1 | a0001c0001t0001g0006 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.183+4789_183+4802d others(16): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61849056 | |||||||
| chr2:61849056 | TTATATAT others(45): Show |
T | 1 | a0001c0001t0017g0117 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.183+4751_183+4802d others(54): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61849056 | |||||||
| chr2:61849058 | A | T | 4 | a0004c0005t0002g0249 a0004c0005t0005g0048 a0004c0005t0005g0049 others(1): Show |
5 | HG02280.hp1 HG02451.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.183+4801T>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61849058 | |||||||
| chr2:61849059 | T | A | 1 | a0001c0001t0001g0107 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.183+4800A>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61849059 | |||||||
| chr2:61849062 | A | ATATATTT others(17): Show |
1 | a0003c0004t0003g0166 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.183+4796_183+4797i others(26): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61849062 | |||||||
| chr2:61849062 | A | ATATT | 23 | a0001c0001t0002g0004 a0001c0001t0002g0016 a0001c0001t0002g0017 others(20): Show |
33 | HG01109.hp1 HG01167.hp2 HG01257.hp2 others(30): Show |
intron_variant | MODIFIER | c.183+4796_183+4797i others(6): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61849062 | |||||||
| chr2:61849062 | A | ATATTTTT others(67): Show |
4 | a0001c0001t0002g0192 a0001c0001t0002g0193 a0001c0001t0002g0194 others(1): Show |
4 | NA18939.hp2 NA18985.hp2 NA18992.hp2 others(1): Show |
intron_variant | MODIFIER | c.183+4796_183+4797i others(76): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61849062 | |||||||
| chr2:61849062 | A | ATATTTTT others(55): Show |
3 | a0001c0001t0002g0197 a0001c0001t0002g0198 a0014c0009t0002g0196 |
3 | HG02602.hp2 NA18955.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.183+4796_183+4797i others(64): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61849062 | |||||||
| chr2:61849062 | A | T | 7 | a0001c0001t0001g0030 a0001c0001t0001g0101 a0001c0001t0001g0120 others(4): Show |
9 | HG01175.hp2 HG02965.hp2 HG03688.hp1 others(6): Show |
intron_variant | MODIFIER | c.183+4797T>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61849062 | |||||||
| chr2:61849063 | TATATAA | T | 28 | a0001c0001t0001g0001 a0002c0002t0002g0224 a0003c0004t0003g0003 others(25): Show |
41 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(38): Show |
intron_variant | MODIFIER | c.183+4790_183+4795d others(8): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61849063 | |||||||
| chr2:61849063 | TATATAAA others(25): Show |
T | 1 | a0001c0001t0002g0239 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.183+4764_183+4795d others(34): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61849063 | |||||||
| chr2:61849064 | A | T | 1 | a0004c0005t0005g0049 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.183+4795T>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61849064 | |||||||
| chr2:61849065 | TATAAATA others(23): Show |
T | 36 | a0001c0001t0001g0113 a0001c0001t0002g0009 a0001c0001t0002g0174 others(33): Show |
50 | HG00323.hp2 HG00408.hp1 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.183+4764_183+4793d others(32): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61849065 | |||||||
| chr2:61849066 | A | T | 2 | a0001c0001t0002g0258 a0005c0010t0018g0262 |
2 | HG02622.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.183+4793T>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61849066 | |||||||
| chr2:61849068 | A | T | 1 | a0001c0001t0002g0266 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.183+4791T>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61849068 | |||||||
| chr2:61849069 | A | T | 40 | a0001c0001t0001g0030 a0001c0001t0001g0101 a0001c0001t0001g0107 others(37): Show |
53 | HG00642.hp1 HG01109.hp1 HG01167.hp2 others(50): Show |
intron_variant | MODIFIER | c.183+4790T>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61849069 | |||||||
| chr2:61849070 | A | T | 156 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(153): Show |
225 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(222): Show |
intron_variant | MODIFIER | c.183+4789T>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61849070 | |||||||
| chr2:61849072 | A | T | 4 | a0001c0001t0002g0260 a0004c0005t0005g0049 a0005c0007t0009g0263 others(1): Show |
4 | HG02572.hp1 HG03098.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.183+4787T>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61849072 | |||||||
| chr2:61849076 | A | T | 3 | a0001c0001t0002g0258 a0001c0001t0002g0266 a0005c0010t0018g0262 |
3 | HG02622.hp1 HG02630.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.183+4783T>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61849076 | |||||||
| chr2:61849080 | T | A | 3 | a0001c0001t0002g0258 a0001c0001t0002g0266 a0005c0010t0018g0262 |
3 | HG02622.hp1 HG02630.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.183+4779A>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61849080 | |||||||
| chr2:61849082 | A | T | 1 | a0001c0001t0001g0097 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.183+4777T>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61849082 | |||||||
| chr2:61849084 | A | T | 2 | a0001c0001t0002g0266 a0005c0010t0018g0262 |
2 | HG02622.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.183+4775T>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61849084 | |||||||
| chr2:61849086 | A | T | 1 | a0001c0001t0002g0258 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.183+4773T>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61849086 | |||||||
| chr2:61849088 | ATATT | A | 7 | a0001c0001t0002g0260 a0004c0005t0002g0249 a0004c0005t0005g0048 others(4): Show |
9 | HG02280.hp1 HG02451.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.183+4767_183+4770d others(6): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61849088 | |||||||
| chr2:61849092 | T | A | 4 | a0001c0001t0002g0258 a0001c0001t0002g0266 a0001c0003t0001g0012 others(1): Show |
4 | HG02622.hp1 HG02630.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.183+4767A>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61849092 | |||||||
| chr2:61849092 | TTAAATA | T | 4 | a0002c0002t0002g0224 a0002c0002t0002g0231 a0006c0008t0002g0215 others(1): Show |
4 | HG03704.hp2 HG04199.hp1 NA18993.hp2 others(1): Show |
intron_variant | MODIFIER | c.183+4761_183+4766d others(8): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61849092 | |||||||
| chr2:61849094 | A | T | 1 | a0001c0003t0001g0012 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.183+4765T>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61849094 | |||||||
| chr2:61849095 | A | T | 126 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(123): Show |
199 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(196): Show |
intron_variant | MODIFIER | c.183+4764T>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61849095 | |||||||
| chr2:61849098 | A | T | 38 | a0001c0001t0001g0113 a0001c0001t0002g0009 a0001c0001t0002g0174 others(35): Show |
52 | HG00323.hp2 HG00408.hp1 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.183+4761T>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61849098 | |||||||
| chr2:61849106 | TTA | T | 32 | a0001c0001t0001g0122 a0001c0001t0002g0004 a0001c0001t0002g0016 others(29): Show |
46 | HG00741.hp1 HG01109.hp1 HG01175.hp2 others(43): Show |
intron_variant | MODIFIER | c.183+4751_183+4752d others(4): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61849106 | |||||||
| chr2:61849121 | A | T | 1 | a0001c0001t0001g0121 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.183+4738T>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61849121 | |||||||
| chr2:61849136 | ATATATAT others(13): Show |
A | 1 | a0001c0001t0002g0200 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.183+4703_183+4722d others(22): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61849136 | |||||||
| chr2:61849140 | ATATTTAT others(5): Show |
A | 4 | a0001c0001t0002g0260 a0001c0001t0002g0265 a0001c0001t0002g0266 others(1): Show |
4 | HG02630.hp1 HG03098.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.183+4707_183+4718d others(14): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61849140 | |||||||
| chr2:61849293 | G | A | 1 | a0001c0001t0004g0092 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.183+4566C>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61849293 | |||||||
| chr2:61849415 | G | A | 1 | a0001c0003t0001g0158 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.183+4444C>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61849415 | |||||||
| chr2:61849443 | C | A | 1 | a0001c0001t0002g0239 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.183+4416G>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61849443 | |||||||
| chr2:61849676 | TCAGGAGG others(6): Show |
T | 2 | a0001c0001t0001g0030 a0001c0001t0001g0101 |
3 | NA18947.hp2 NA19064.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.183+4170_183+4182d others(15): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61849676 | |||||||
| chr2:61849775 | C | T | 1 | a0011c0018t0015g0261 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.183+4084G>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61849775 | |||||||
| chr2:61849783 | C | CA | 8 | a0001c0001t0001g0093 a0001c0001t0001g0107 a0001c0001t0001g0108 others(5): Show |
9 | HG01081.hp2 HG01099.hp2 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.183+4075dupT | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61849783 | |||||||
| chr2:61849857 | A | G | 1 | a0001c0001t0004g0055 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.183+4002T>C | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61849857 | |||||||
| chr2:61849865 | T | TAACACAG others(1): Show |
268 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(265): Show |
395 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(392): Show |
intron_variant | MODIFIER | c.183+3993_183+3994i others(10): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61849865 | |||||||
| chr2:61849884 | A | C | 1 | a0003c0004t0003g0159 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.183+3975T>G | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61849884 | |||||||
| chr2:61849885 | C | T | 1 | a0003c0004t0003g0159 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.183+3974G>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61849885 | |||||||
| chr2:61849892 | T | A | 1 | a0003c0004t0003g0159 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.183+3967A>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61849892 | |||||||
| chr2:61849901 | G | T | 1 | a0003c0004t0003g0159 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.183+3958C>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61849901 | |||||||
| chr2:61850004 | T | G | 1 | a0001c0001t0001g0108 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.183+3855A>C | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61850004 | |||||||
| chr2:61850128 | A | T | 1 | a0009c0011t0002g0247 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.183+3731T>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61850128 | |||||||
| chr2:61850159 | G | A | 1 | a0002c0002t0002g0240 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.183+3700C>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61850159 | |||||||
| chr2:61850171 | C | T | 1 | a0002c0002t0002g0202 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.183+3688G>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61850171 | |||||||
| chr2:61850256 | C | T | 2 | a0001c0001t0001g0107 a0001c0001t0001g0108 |
2 | HG01243.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.183+3603G>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61850256 | |||||||
| chr2:61850258 | T | C | 1 | a0003c0004t0003g0173 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.183+3601A>G | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61850258 | |||||||
| chr2:61850454 | T | C | 26 | a0003c0004t0003g0003 a0003c0004t0003g0015 a0003c0004t0003g0031 others(23): Show |
39 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(36): Show |
intron_variant | MODIFIER | c.183+3405A>G | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61850454 | |||||||
| chr2:61850489 | C | T | 1 | a0001c0001t0001g0120 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.183+3370G>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61850489 | |||||||
| chr2:61850525 | G | A | 2 | a0001c0001t0001g0050 a0001c0001t0001g0259 |
3 | HG02280.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.183+3334C>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61850525 | |||||||
| chr2:61850614 | G | A | 2 | a0001c0001t0002g0265 a0001c0001t0002g0266 |
2 | HG02630.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.183+3245C>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61850614 | |||||||
| chr2:61850790 | C | A | 268 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(265): Show |
395 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(392): Show |
intron_variant | MODIFIER | c.183+3069G>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61850790 | |||||||
| chr2:61850929 | C | G | 1 | a0001c0001t0004g0054 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.183+2930G>C | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61850929 | |||||||
| chr2:61851036 | G | T | 1 | a0001c0001t0001g0119 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.183+2823C>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61851036 | |||||||
| chr2:61851104 | C | A | 1 | a0001c0001t0001g0094 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.183+2755G>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61851104 | |||||||
| chr2:61851166 | G | A | 66 | a0001c0001t0001g0113 a0001c0001t0002g0009 a0001c0001t0002g0112 others(63): Show |
89 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(86): Show |
intron_variant | MODIFIER | c.183+2693C>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61851166 | |||||||
| chr2:61851194 | G | A | 137 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0113 others(134): Show |
187 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.183+2665C>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61851194 | |||||||
| chr2:61851360 | A | G | 268 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(265): Show |
395 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(392): Show |
intron_variant | MODIFIER | c.183+2499T>C | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61851360 | |||||||
| chr2:61851455 | C | T | 130 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(127): Show |
207 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.183+2404G>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61851455 | |||||||
| chr2:61851514 | T | C | 4 | a0004c0005t0002g0249 a0004c0005t0005g0048 a0004c0005t0005g0049 others(1): Show |
6 | HG02280.hp1 HG02451.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.183+2345A>G | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61851514 | |||||||
| chr2:61851642 | C | T | 7 | a0001c0001t0002g0260 a0001c0001t0002g0265 a0001c0001t0002g0266 others(4): Show |
7 | HG02572.hp1 HG02622.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.183+2217G>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61851642 | |||||||
| chr2:61851730 | C | T | 2 | a0003c0004t0003g0031 a0003c0004t0003g0118 |
3 | HG00140.hp1 HG01081.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.183+2129G>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61851730 | |||||||
| chr2:61851810 | T | G | 2 | a0002c0002t0002g0116 a0002c0002t0002g0241 |
2 | HG02523.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.183+2049A>C | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61851810 | |||||||
| chr2:61851814 | G | C | 2 | a0001c0001t0001g0095 a0001c0001t0001g0096 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.183+2045C>G | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61851814 | |||||||
| chr2:61851943 | A | G | 1 | a0001c0001t0017g0117 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.183+1916T>C | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61851943 | |||||||
| chr2:61852132 | T | G | 35 | a0001c0001t0002g0004 a0001c0001t0002g0016 a0001c0001t0002g0017 others(32): Show |
49 | HG01109.hp1 HG01167.hp2 HG01175.hp2 others(46): Show |
intron_variant | MODIFIER | c.183+1727A>C | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61852132 | |||||||
| chr2:61852319 | C | G | 1 | a0001c0001t0016g0102 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.183+1540G>C | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61852319 | |||||||
| chr2:61852408 | C | G | 2 | a0001c0001t0001g0052 a0001c0001t0001g0053 |
2 | HG00642.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.183+1451G>C | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61852408 | |||||||
| chr2:61852515 | G | C | 1 | a0001c0001t0001g0111 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.183+1344C>G | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61852515 | |||||||
| chr2:61852582 | C | G | 2 | a0001c0001t0001g0050 a0001c0001t0001g0259 |
3 | HG02280.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.183+1277G>C | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61852582 | |||||||
| chr2:61852760 | T | C | 62 | a0001c0001t0001g0113 a0001c0001t0002g0009 a0001c0001t0002g0112 others(59): Show |
85 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(82): Show |
intron_variant | MODIFIER | c.183+1099A>G | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61852760 | |||||||
| chr2:61852846 | A | G | 2 | a0001c0001t0001g0030 a0001c0001t0001g0101 |
3 | NA18947.hp2 NA19064.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.183+1013T>C | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61852846 | |||||||
| chr2:61852938 | CT | C | 226 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(223): Show |
344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.183+920delA | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61852938 | |||||||
| chr2:61852938 | CTT | C | 22 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0050 others(19): Show |
28 | HG01515.hp2 HG01981.hp2 HG02280.hp1 others(25): Show |
intron_variant | MODIFIER | c.183+919_183+920del others(2): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61852938 | |||||||
| chr2:61853045 | A | G | 268 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(265): Show |
395 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(392): Show |
intron_variant | MODIFIER | c.183+814T>C | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61853045 | |||||||
| chr2:61853056 | G | T | 268 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(265): Show |
395 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(392): Show |
intron_variant | MODIFIER | c.183+803C>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61853056 | |||||||
| chr2:61853109 | A | G | 1 | a0003c0004t0003g0100 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.183+750T>C | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61853109 | |||||||
| chr2:61853184 | A | G | 1 | a0001c0001t0001g0099 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.183+675T>C | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61853184 | |||||||
| chr2:61853200 | G | A | 1 | a0001c0001t0001g0257 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.183+659C>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61853200 | |||||||
| chr2:61853201 | C | A | 1 | a0001c0001t0001g0257 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.183+658G>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61853201 | |||||||
| chr2:61853214 | T | C | 1 | a0001c0001t0002g0258 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.183+645A>G | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61853214 | |||||||
| chr2:61853250 | C | T | 1 | a0001c0003t0001g0098 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.183+609G>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61853250 | |||||||
| chr2:61853288 | T | A | 2 | a0001c0001t0001g0050 a0001c0001t0001g0259 |
3 | HG02280.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.183+571A>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61853288 | |||||||
| chr2:61853338 | A | G | 58 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0022 others(55): Show |
88 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.183+521T>C | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61853338 | |||||||
| chr2:61853347 | G | A | 7 | a0001c0001t0002g0260 a0001c0001t0002g0265 a0001c0001t0002g0266 others(4): Show |
7 | HG02572.hp1 HG02622.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.183+512C>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61853347 | |||||||
| chr2:61853786 | C | G | 1 | a0003c0004t0003g0267 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.183+73G>C | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61853786 | |||||||
| chr2:61853787 | G | C | 1 | a0003c0004t0003g0267 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.183+72C>G | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61853787 |