Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 84070 |
| ensemblid | ENSG00000135436.8 |
| hgncid | 25296 |
| symbol | FAM186B |
| name | family with sequence similarity 186 member B |
| refseq_nuc | NM_032130.3 |
| refseq_prot | NP_115506.1 |
| ensembl_nuc | ENST00000257894.2 |
| ensembl_prot | ENSP00000257894.2 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 49587505 |
| end | 49605639 |
| strand | - |
| ver | v1.2 |
| region | chr12:49587505-49605639 |
| region5000 | chr12:49582505-49610639 |
| regionname0 | FAM186B_chr12_49587505_49605639 |
| regionname5000 | FAM186B_chr12_49582505_49610639 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 893 | 171 | 26 | 51 | 51 | 10 | 31 | 35 | FAM186B_chr12_49582505_49610639 | FAM186B | MEKDD others(888): Show |
chr12 | 49582505 | 49610639 |
| a0002 | 0/0 | 893 | 36 | 8 | 10 | 14 | 2 | 2 | 11 | FAM186B_chr12_49582505_49610639 | FAM186B | MEKDD others(888): Show |
chr12 | 49582505 | 49610639 |
| a0003 | 0/0 | 893 | 13 | 12 | 1 | 0 | 0 | 0 | 0 | FAM186B_chr12_49582505_49610639 | FAM186B | MEKDD others(888): Show |
chr12 | 49582505 | 49610639 |
| a0004 | 0/0 | 893 | 12 | 11 | 1 | 0 | 0 | 0 | 0 | FAM186B_chr12_49582505_49610639 | FAM186B | MEKDD others(888): Show |
chr12 | 49582505 | 49610639 |
| a0005 | 0/0 | 893 | 11 | 11 | 0 | 0 | 0 | 0 | 0 | FAM186B_chr12_49582505_49610639 | FAM186B | MEKDD others(888): Show |
chr12 | 49582505 | 49610639 |
| a0006 | 0/0 | 893 | 9 | 9 | 0 | 0 | 0 | 0 | 0 | FAM186B_chr12_49582505_49610639 | FAM186B | MEKDD others(888): Show |
chr12 | 49582505 | 49610639 |
| a0007 | 0/0 | 893 | 3 | 0 | 0 | 3 | 0 | 0 | 2 | FAM186B_chr12_49582505_49610639 | FAM186B | MEKDD others(888): Show |
chr12 | 49582505 | 49610639 |
| a0008 | 0/0 | 893 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | FAM186B_chr12_49582505_49610639 | FAM186B | MEKDD others(888): Show |
chr12 | 49582505 | 49610639 |
| a0009 | 0/0 | 893 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | FAM186B_chr12_49582505_49610639 | FAM186B | MEKDD others(888): Show |
chr12 | 49582505 | 49610639 |
| a0010 | 0/0 | 461 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FAM186B_chr12_49582505_49610639 | FAM186B | MEKDD others(456): Show |
chr12 | 49582505 | 49610639 |
| a0011 | 0/0 | 893 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM186B_chr12_49582505_49610639 | FAM186B | MEKDD others(888): Show |
chr12 | 49582505 | 49610639 |
| a0012 | 0/0 | 893 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM186B_chr12_49582505_49610639 | FAM186B | MEKDD others(888): Show |
chr12 | 49582505 | 49610639 |
| a0013 | 0/0 | 893 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM186B_chr12_49582505_49610639 | FAM186B | MEKDD others(888): Show |
chr12 | 49582505 | 49610639 |
| a0014 | 0/0 | 893 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FAM186B_chr12_49582505_49610639 | FAM186B | MEKDD others(888): Show |
chr12 | 49582505 | 49610639 |
| a0015 | 0/0 | 893 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FAM186B_chr12_49582505_49610639 | FAM186B | MEKDD others(888): Show |
chr12 | 49582505 | 49610639 |
| a0016 | 0/0 | 893 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FAM186B_chr12_49582505_49610639 | FAM186B | MEKDD others(888): Show |
chr12 | 49582505 | 49610639 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2679 | 166 | 23 | 49 | 51 | 10 | 31 | FAM186B_chr12_49582505_49610639 | FAM186B | ATGGA others(2674): Show |
chr12 | 49582505 | 49610639 | ||
| a0001c0007 | 0/0 | 2679 | 4 | 2 | 2 | 0 | 0 | 0 | FAM186B_chr12_49582505_49610639 | FAM186B | ATGGA others(2674): Show |
chr12 | 49582505 | 49610639 | ||
| a0001c0014 | 0/0 | 2679 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186B_chr12_49582505_49610639 | FAM186B | ATGGA others(2674): Show |
chr12 | 49582505 | 49610639 | ||
| a0002c0002 | 0/0 | 2679 | 36 | 8 | 10 | 14 | 2 | 2 | FAM186B_chr12_49582505_49610639 | FAM186B | ATGGA others(2674): Show |
chr12 | 49582505 | 49610639 | ||
| a0003c0003 | 0/0 | 2679 | 13 | 12 | 1 | 0 | 0 | 0 | FAM186B_chr12_49582505_49610639 | FAM186B | ATGGA others(2674): Show |
chr12 | 49582505 | 49610639 | ||
| a0004c0004 | 0/0 | 2679 | 12 | 11 | 1 | 0 | 0 | 0 | FAM186B_chr12_49582505_49610639 | FAM186B | ATGGA others(2674): Show |
chr12 | 49582505 | 49610639 | ||
| a0005c0005 | 0/0 | 2679 | 11 | 11 | 0 | 0 | 0 | 0 | FAM186B_chr12_49582505_49610639 | FAM186B | ATGGA others(2674): Show |
chr12 | 49582505 | 49610639 | ||
| a0006c0006 | 0/0 | 2679 | 7 | 7 | 0 | 0 | 0 | 0 | FAM186B_chr12_49582505_49610639 | FAM186B | ATGGA others(2674): Show |
chr12 | 49582505 | 49610639 | ||
| a0006c0010 | 0/0 | 2679 | 2 | 2 | 0 | 0 | 0 | 0 | FAM186B_chr12_49582505_49610639 | FAM186B | ATGGA others(2674): Show |
chr12 | 49582505 | 49610639 | ||
| a0007c0008 | 0/0 | 2679 | 3 | 0 | 0 | 3 | 0 | 0 | FAM186B_chr12_49582505_49610639 | FAM186B | ATGGA others(2674): Show |
chr12 | 49582505 | 49610639 | ||
| a0008c0009 | 0/0 | 2679 | 2 | 2 | 0 | 0 | 0 | 0 | FAM186B_chr12_49582505_49610639 | FAM186B | ATGGA others(2674): Show |
chr12 | 49582505 | 49610639 | ||
| a0009c0011 | 0/0 | 2679 | 2 | 2 | 0 | 0 | 0 | 0 | FAM186B_chr12_49582505_49610639 | FAM186B | ATGGA others(2674): Show |
chr12 | 49582505 | 49610639 | ||
| a0010c0019 | 0/0 | 2698 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186B_chr12_49582505_49610639 | FAM186B | ATGGA others(2693): Show |
chr12 | 49582505 | 49610639 | ||
| a0011c0013 | 0/0 | 2679 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186B_chr12_49582505_49610639 | FAM186B | ATGGA others(2674): Show |
chr12 | 49582505 | 49610639 | ||
| a0012c0012 | 0/0 | 2679 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186B_chr12_49582505_49610639 | FAM186B | ATGGA others(2674): Show |
chr12 | 49582505 | 49610639 | ||
| a0013c0016 | 0/0 | 2679 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186B_chr12_49582505_49610639 | FAM186B | ATGGA others(2674): Show |
chr12 | 49582505 | 49610639 | ||
| a0014c0017 | 0/0 | 2679 | 1 | 0 | 0 | 0 | 0 | 1 | FAM186B_chr12_49582505_49610639 | FAM186B | ATGGA others(2674): Show |
chr12 | 49582505 | 49610639 | ||
| a0015c0015 | 0/0 | 2679 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186B_chr12_49582505_49610639 | FAM186B | ATGGA others(2674): Show |
chr12 | 49582505 | 49610639 | ||
| a0016c0018 | 0/0 | 2679 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186B_chr12_49582505_49610639 | FAM186B | ATGGA others(2674): Show |
chr12 | 49582505 | 49610639 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2944 | 161 | 23 | 49 | 46 | 10 | 31 | FAM186B_chr12_49582505_49610639 | FAM186B | AGTTG others(2939): Show |
chr12 | 49582505 | 49610639 |
| a0001c0001t0003 | 0/0 | 2944 | 5 | 0 | 0 | 5 | 0 | 0 | FAM186B_chr12_49582505_49610639 | FAM186B | AGTTG others(2939): Show |
chr12 | 49582505 | 49610639 |
| a0001c0007t0001 | 0/0 | 2944 | 4 | 2 | 2 | 0 | 0 | 0 | FAM186B_chr12_49582505_49610639 | FAM186B | AGTTG others(2939): Show |
chr12 | 49582505 | 49610639 |
| a0001c0014t0001 | 0/0 | 2944 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186B_chr12_49582505_49610639 | FAM186B | AGTTG others(2939): Show |
chr12 | 49582505 | 49610639 |
| a0002c0002t0001 | 0/0 | 2944 | 34 | 6 | 10 | 14 | 2 | 2 | FAM186B_chr12_49582505_49610639 | FAM186B | AGTTG others(2939): Show |
chr12 | 49582505 | 49610639 |
| a0002c0002t0004 | 0/0 | 2944 | 2 | 2 | 0 | 0 | 0 | 0 | FAM186B_chr12_49582505_49610639 | FAM186B | AGTTG others(2939): Show |
chr12 | 49582505 | 49610639 |
| a0003c0003t0001 | 0/0 | 2944 | 13 | 12 | 1 | 0 | 0 | 0 | FAM186B_chr12_49582505_49610639 | FAM186B | AGTTG others(2939): Show |
chr12 | 49582505 | 49610639 |
| a0004c0004t0001 | 0/0 | 2944 | 12 | 11 | 1 | 0 | 0 | 0 | FAM186B_chr12_49582505_49610639 | FAM186B | AGTTG others(2939): Show |
chr12 | 49582505 | 49610639 |
| a0005c0005t0001 | 0/0 | 2944 | 11 | 11 | 0 | 0 | 0 | 0 | FAM186B_chr12_49582505_49610639 | FAM186B | AGTTG others(2939): Show |
chr12 | 49582505 | 49610639 |
| a0006c0006t0002 | 0/0 | 2944 | 7 | 7 | 0 | 0 | 0 | 0 | FAM186B_chr12_49582505_49610639 | FAM186B | AGTTG others(2939): Show |
chr12 | 49582505 | 49610639 |
| a0006c0010t0002 | 0/0 | 2944 | 2 | 2 | 0 | 0 | 0 | 0 | FAM186B_chr12_49582505_49610639 | FAM186B | AGTTG others(2939): Show |
chr12 | 49582505 | 49610639 |
| a0007c0008t0001 | 0/0 | 2944 | 3 | 0 | 0 | 3 | 0 | 0 | FAM186B_chr12_49582505_49610639 | FAM186B | AGTTG others(2939): Show |
chr12 | 49582505 | 49610639 |
| a0008c0009t0001 | 0/0 | 2944 | 2 | 2 | 0 | 0 | 0 | 0 | FAM186B_chr12_49582505_49610639 | FAM186B | AGTTG others(2939): Show |
chr12 | 49582505 | 49610639 |
| a0009c0011t0001 | 0/0 | 2944 | 2 | 2 | 0 | 0 | 0 | 0 | FAM186B_chr12_49582505_49610639 | FAM186B | AGTTG others(2939): Show |
chr12 | 49582505 | 49610639 |
| a0010c0019t0001 | 0/0 | 2963 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186B_chr12_49582505_49610639 | FAM186B | AGTTG others(2958): Show |
chr12 | 49582505 | 49610639 |
| a0011c0013t0001 | 0/0 | 2944 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186B_chr12_49582505_49610639 | FAM186B | AGTTG others(2939): Show |
chr12 | 49582505 | 49610639 |
| a0012c0012t0001 | 0/0 | 2944 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186B_chr12_49582505_49610639 | FAM186B | AGTTG others(2939): Show |
chr12 | 49582505 | 49610639 |
| a0013c0016t0001 | 0/0 | 2944 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186B_chr12_49582505_49610639 | FAM186B | AGTTG others(2939): Show |
chr12 | 49582505 | 49610639 |
| a0014c0017t0001 | 0/0 | 2944 | 1 | 0 | 0 | 0 | 0 | 1 | FAM186B_chr12_49582505_49610639 | FAM186B | AGTTG others(2939): Show |
chr12 | 49582505 | 49610639 |
| a0015c0015t0001 | 0/0 | 2944 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186B_chr12_49582505_49610639 | FAM186B | AGTTG others(2939): Show |
chr12 | 49582505 | 49610639 |
| a0016c0018t0001 | 0/0 | 2944 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186B_chr12_49582505_49610639 | FAM186B | AGTTG others(2939): Show |
chr12 | 49582505 | 49610639 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 36 | 0 | 11 | 14 | 2 | 9 | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| a0001c0001t0001g0002 | 0/0 | 32 | 8 | 9 | 7 | 3 | 5 | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| a0001c0001t0001g0005 | 0/0 | 7 | 0 | 7 | 0 | 0 | 0 | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| a0001c0001t0001g0006 | 0/0 | 7 | 0 | 2 | 0 | 2 | 3 | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| a0001c0001t0001g0009 | 0/0 | 6 | 0 | 1 | 4 | 0 | 1 | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| a0001c0001t0001g0010 | 0/0 | 6 | 2 | 1 | 1 | 0 | 2 | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| a0001c0001t0001g0011 | 0/0 | 5 | 0 | 0 | 4 | 1 | 0 | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| a0001c0001t0001g0016 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| a0001c0001t0001g0021 | 0/1 | 3 | 0 | 2 | 0 | 0 | 0 | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| a0001c0001t0001g0022 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| a0001c0001t0001g0023 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| a0001c0001t0001g0024 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| a0001c0001t0001g0025 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| a0001c0001t0001g0026 | 1/0 | 3 | 0 | 2 | 0 | 0 | 0 | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| a0001c0001t0001g0034 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| a0001c0001t0003g0015 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| a0001c0001t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| a0001c0007t0001g0012 | 0/0 | 4 | 2 | 2 | 0 | 0 | 0 | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| a0001c0014t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| a0002c0002t0001g0003 | 0/0 | 8 | 2 | 2 | 2 | 1 | 1 | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| a0002c0002t0001g0004 | 0/0 | 7 | 0 | 1 | 5 | 1 | 0 | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| a0002c0002t0001g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| a0002c0002t0001g0014 | 0/0 | 4 | 0 | 1 | 2 | 0 | 1 | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| a0002c0002t0001g0018 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| a0002c0002t0001g0031 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| a0002c0002t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| a0002c0002t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| a0002c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| a0002c0002t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| a0002c0002t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| a0002c0002t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| a0002c0002t0004g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| a0002c0002t0004g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| a0003c0003t0001g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| a0003c0003t0001g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| a0003c0003t0001g0020 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| a0003c0003t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| a0003c0003t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| a0003c0003t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| a0004c0004t0001g0007 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| a0004c0004t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| a0004c0004t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| a0004c0004t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| a0004c0004t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| a0004c0004t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| a0005c0005t0001g0008 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| a0005c0005t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| a0005c0005t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| a0005c0005t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| a0005c0005t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| a0006c0006t0002g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| a0006c0006t0002g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| a0006c0006t0002g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| a0006c0006t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| a0006c0006t0002g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| a0006c0010t0002g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| a0007c0008t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| a0007c0008t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| a0008c0009t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| a0008c0009t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| a0009c0011t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| a0009c0011t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| a0010c0019t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| a0011c0013t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| a0012c0012t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| a0013c0016t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| a0014c0017t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| a0015c0015t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| a0016c0018t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0077 | EUR | GBR | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0011 | EUR | GBR | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0006 | EUR | FIN | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG00280 | hp2 | a0002 | c0002 | t0001 | g0004 | EUR | FIN | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG00423 | hp1 | a0007 | c0008 | t0001 | g0028 | EAS | CHS | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | CHS | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG00639 | hp2 | a0002 | c0002 | t0001 | g0018 | AMR | PUR | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG01071 | hp1 | a0003 | c0003 | t0001 | g0020 | AMR | PUR | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG01106 | hp1 | a0002 | c0002 | t0001 | g0003 | AMR | PUR | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG01106 | hp2 | a0002 | c0002 | t0001 | g0018 | AMR | PUR | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG01109 | hp1 | a0004 | c0004 | t0001 | g0051 | AMR | PUR | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG01167 | hp1 | a0001 | c0007 | t0001 | g0012 | AMR | PUR | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG01167 | hp2 | a0002 | c0002 | t0001 | g0031 | AMR | PUR | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG01168 | hp2 | a0010 | c0019 | t0001 | g0090 | AMR | PUR | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG01169 | hp1 | a0001 | c0007 | t0001 | g0012 | AMR | PUR | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG01175 | hp1 | a0002 | c0002 | t0001 | g0014 | AMR | PUR | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG01192 | hp1 | a0002 | c0002 | t0001 | g0018 | AMR | PUR | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG01361 | hp1 | a0002 | c0002 | t0001 | g0059 | AMR | CLM | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | CLM | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | CLM | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | CLM | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0025 | EUR | IBS | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0006 | EUR | IBS | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG01884 | hp1 | a0004 | c0004 | t0001 | g0007 | AFR | ACB | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG01884 | hp2 | a0006 | c0006 | t0002 | g0038 | AFR | ACB | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG01891 | hp2 | a0005 | c0005 | t0001 | g0008 | AFR | ACB | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PEL | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PEL | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0095 | AMR | PEL | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG01978 | hp2 | a0002 | c0002 | t0001 | g0003 | AMR | PEL | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | PEL | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG02004 | hp2 | a0002 | c0002 | t0001 | g0054 | AMR | PEL | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG02015 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | KHV | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | KHV | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG02055 | hp1 | a0003 | c0003 | t0001 | g0068 | AFR | ACB | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG02055 | hp2 | a0006 | c0006 | t0002 | g0038 | AFR | ACB | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG02056 | hp2 | a0001 | c0001 | t0003 | g0082 | EAS | KHV | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | KHV | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG02080 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | KHV | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | KHV | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG02135 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | KHV | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG02145 | hp1 | a0001 | c0007 | t0001 | g0012 | AFR | ACB | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG02145 | hp2 | a0004 | c0004 | t0001 | g0029 | AFR | ACB | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | PEL | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG02257 | hp2 | a0008 | c0009 | t0001 | g0079 | AFR | ACB | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG02258 | hp1 | a0011 | c0013 | t0001 | g0053 | AFR | ACB | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | PEL | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG02293 | hp2 | a0002 | c0002 | t0001 | g0004 | AMR | PEL | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0071 | AMR | PEL | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PEL | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG02451 | hp1 | a0001 | c0007 | t0001 | g0012 | AFR | ACB | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG02451 | hp2 | a0001 | c0014 | t0001 | g0066 | AFR | ACB | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG02572 | hp1 | a0003 | c0003 | t0001 | g0030 | AFR | GWD | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG02615 | hp1 | a0005 | c0005 | t0001 | g0008 | AFR | GWD | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG02630 | hp1 | a0004 | c0004 | t0001 | g0007 | AFR | GWD | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | GWD | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG02647 | hp1 | a0003 | c0003 | t0001 | g0017 | AFR | GWD | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG02647 | hp2 | a0005 | c0005 | t0001 | g0062 | AFR | GWD | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG02717 | hp2 | a0012 | c0012 | t0001 | g0049 | AFR | GWD | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG02723 | hp1 | a0002 | c0002 | t0001 | g0003 | AFR | GWD | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG02723 | hp2 | a0003 | c0003 | t0001 | g0017 | AFR | GWD | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0034 | SAS | PJL | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0033 | SAS | PJL | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG02809 | hp2 | a0006 | c0010 | t0002 | g0037 | AFR | GWD | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG02818 | hp1 | a0004 | c0004 | t0001 | g0052 | AFR | GWD | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG02818 | hp2 | a0004 | c0004 | t0001 | g0007 | AFR | GWD | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG02886 | hp1 | a0005 | c0005 | t0001 | g0063 | AFR | GWD | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | GWD | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG02896 | hp1 | a0003 | c0003 | t0001 | g0017 | AFR | GWD | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG02896 | hp2 | a0002 | c0002 | t0004 | g0102 | AFR | GWD | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG02897 | hp1 | a0002 | c0002 | t0004 | g0103 | AFR | GWD | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG02897 | hp2 | a0004 | c0004 | t0001 | g0007 | AFR | GWD | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG02922 | hp1 | a0003 | c0003 | t0001 | g0020 | AFR | ESN | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG02922 | hp2 | a0006 | c0010 | t0002 | g0037 | AFR | ESN | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | ESN | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG02976 | hp2 | a0006 | c0006 | t0002 | g0039 | AFR | ESN | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG03041 | hp1 | a0008 | c0009 | t0001 | g0078 | AFR | GWD | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG03041 | hp2 | a0005 | c0005 | t0001 | g0008 | AFR | GWD | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG03098 | hp1 | a0006 | c0006 | t0002 | g0099 | AFR | MSL | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG03098 | hp2 | a0005 | c0005 | t0001 | g0032 | AFR | MSL | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG03130 | hp1 | a0004 | c0004 | t0001 | g0007 | AFR | ESN | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG03130 | hp2 | a0003 | c0003 | t0001 | g0019 | AFR | ESN | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG03195 | hp1 | a0005 | c0005 | t0001 | g0091 | AFR | ESN | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG03195 | hp2 | a0002 | c0002 | t0001 | g0003 | AFR | ESN | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG03209 | hp1 | a0003 | c0003 | t0001 | g0069 | AFR | MSL | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | MSL | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | MSL | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG03225 | hp2 | a0013 | c0016 | t0001 | g0058 | AFR | MSL | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG03453 | hp1 | a0006 | c0006 | t0002 | g0100 | AFR | MSL | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG03453 | hp2 | a0005 | c0005 | t0001 | g0008 | AFR | MSL | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG03486 | hp1 | a0003 | c0003 | t0001 | g0020 | AFR | MSL | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | MSL | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0081 | SAS | PJL | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0025 | SAS | PJL | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG03516 | hp1 | a0002 | c0002 | t0001 | g0056 | AFR | ESN | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG03516 | hp2 | a0004 | c0004 | t0001 | g0050 | AFR | ESN | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG03540 | hp2 | a0006 | c0006 | t0002 | g0101 | AFR | GWD | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG03579 | hp1 | a0005 | c0005 | t0001 | g0032 | AFR | MSL | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | MSL | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG03688 | hp1 | a0014 | c0017 | t0001 | g0088 | SAS | STU | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | STU | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG03704 | hp1 | a0002 | c0002 | t0001 | g0003 | SAS | PJL | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0044 | SAS | BEB | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0072 | SAS | BEB | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | STU | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0065 | SAS | STU | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0022 | SAS | BEB | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG04184 | hp2 | a0002 | c0002 | t0001 | g0014 | SAS | BEB | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | STU | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0064 | SAS | STU | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| NA18522 | hp1 | a0004 | c0004 | t0001 | g0007 | AFR | YRI | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| NA18522 | hp2 | a0006 | c0006 | t0002 | g0039 | AFR | YRI | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| NA18906 | hp1 | a0004 | c0004 | t0001 | g0045 | AFR | YRI | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | YRI | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| NA18945 | hp1 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| NA18945 | hp2 | a0002 | c0002 | t0001 | g0013 | EAS | JPT | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| NA18951 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| NA18951 | hp2 | a0002 | c0002 | t0001 | g0014 | EAS | JPT | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| NA18952 | hp2 | a0015 | c0015 | t0001 | g0067 | EAS | JPT | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| NA18961 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| NA18975 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| NA18981 | hp1 | a0007 | c0008 | t0001 | g0028 | EAS | JPT | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| NA18981 | hp2 | a0002 | c0002 | t0001 | g0014 | EAS | JPT | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| NA18982 | hp2 | a0016 | c0018 | t0001 | g0061 | EAS | JPT | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| NA18988 | hp2 | a0002 | c0002 | t0001 | g0013 | EAS | JPT | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| NA18990 | hp2 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| NA18998 | hp2 | a0007 | c0008 | t0001 | g0096 | EAS | JPT | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| NA19000 | hp1 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| NA19012 | hp1 | a0002 | c0002 | t0001 | g0013 | EAS | JPT | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | LWK | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| NA19043 | hp2 | a0009 | c0011 | t0001 | g0042 | AFR | LWK | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| NA19067 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| NA19075 | hp2 | a0002 | c0002 | t0001 | g0055 | EAS | JPT | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| NA19083 | hp2 | a0002 | c0002 | t0001 | g0013 | EAS | JPT | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| NA19084 | hp1 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | YRI | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| NA19240 | hp2 | a0005 | c0005 | t0001 | g0008 | AFR | YRI | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | ASW | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| NA20129 | hp2 | a0002 | c0002 | t0001 | g0031 | AFR | ASW | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| NA20805 | hp1 | a0002 | c0002 | t0001 | g0003 | EUR | TSI | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | GIH | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | ACB | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG02109 | hp2 | a0005 | c0005 | t0001 | g0008 | AFR | ACB | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG02486 | hp1 | a0002 | c0002 | t0001 | g0041 | AFR | ACB | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG02486 | hp2 | a0003 | c0003 | t0001 | g0019 | AFR | ACB | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | ACB | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG02559 | hp2 | a0003 | c0003 | t0001 | g0019 | AFR | ACB | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | MSL | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG03471 | hp2 | a0004 | c0004 | t0001 | g0029 | AFR | MSL | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG06807 | hp1 | a0002 | c0002 | t0001 | g0057 | AFR | USA | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| HG06807 | hp2 | a0009 | c0011 | t0001 | g0043 | AFR | USA | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | LWK | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| NA21309 | hp2 | a0003 | c0003 | t0001 | g0030 | AFR | LWK | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0021 | REF | REF | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0026 | REF | REF | FAM186B_chr12_49582505_49610639 | FAM186B | chr12 | 49582505 | 49610639 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:49587715 | C | T | 1 | a0013 | 1 | HG03225.hp2 | missense_variant | MODERATE | c.2572G>A | p.Glu858Lys | FAM186B | ENSG00000135436.8 | transcript | ENST00000257894.2 | protein_coding | 7/7 | 2734/2944 | 2572/2682 | 858/893 | chr12 | 49587715 | |||
| chr12:49588455 | G | A | 1 | a0007 | 3 | HG00423.hp1 NA18981.hp1 NA18998.hp2 |
missense_variant&splice_region_variant | MODERATE | c.2533C>T | p.Arg845Cys | FAM186B | ENSG00000135436.8 | transcript | ENST00000257894.2 | protein_coding | 6/7 | 2695/2944 | 2533/2682 | 845/893 | chr12 | 49588455 | |||
| chr12:49588481 | C | T | 1 | a0012 | 1 | HG02717.hp2 | missense_variant | MODERATE | c.2507G>A | p.Arg836Gln | FAM186B | ENSG00000135436.8 | transcript | ENST00000257894.2 | protein_coding | 6/7 | 2669/2944 | 2507/2682 | 836/893 | chr12 | 49588481 | |||
| chr12:49588536 | G | A | 1 | a0008 | 2 | HG02257.hp2 HG03041.hp1 |
missense_variant | MODERATE | c.2452C>T | p.Arg818Trp | FAM186B | ENSG00000135436.8 | transcript | ENST00000257894.2 | protein_coding | 6/7 | 2614/2944 | 2452/2682 | 818/893 | chr12 | 49588536 | |||
| chr12:49598909 | G | A | 1 | a0006 | 9 | HG01884.hp2 HG02055.hp2 HG02809.hp2 others(6): Show |
missense_variant | MODERATE | c.2210C>T | p.Thr737Met | FAM186B | ENSG00000135436.8 | transcript | ENST00000257894.2 | protein_coding | 5/7 | 2372/2944 | 2210/2682 | 737/893 | chr12 | 49598909 | |||
| chr12:49598939 | G | A | 1 | a0014 | 1 | HG03688.hp1 | missense_variant | MODERATE | c.2180C>T | p.Ala727Val | FAM186B | ENSG00000135436.8 | transcript | ENST00000257894.2 | protein_coding | 5/7 | 2342/2944 | 2180/2682 | 727/893 | chr12 | 49598939 | |||
| chr12:49599850 | G | C | 1 | a0009 | 2 | HG06807.hp2 NA19043.hp2 |
missense_variant | MODERATE | c.1790C>G | p.Ser597Cys | FAM186B | ENSG00000135436.8 | transcript | ENST00000257894.2 | protein_coding | 4/7 | 1952/2944 | 1790/2682 | 597/893 | chr12 | 49599850 | |||
| chr12:49599895 | C | T | 5 | a0002 a0004 a0012 others(2): Show |
51 | HG00280.hp2 HG00639.hp2 HG01106.hp1 others(48): Show |
missense_variant | MODERATE | c.1745G>A | p.Arg582Gln | FAM186B | ENSG00000135436.8 | transcript | ENST00000257894.2 | protein_coding | 4/7 | 1907/2944 | 1745/2682 | 582/893 | chr12 | 49599895 | |||
| chr12:49599983 | C | G | 4 | a0003 a0005 a0009 others(1): Show |
27 | HG01071.hp1 HG01891.hp2 HG02055.hp1 others(24): Show |
missense_variant | MODERATE | c.1657G>C | p.Glu553Gln | FAM186B | ENSG00000135436.8 | transcript | ENST00000257894.2 | protein_coding | 4/7 | 1819/2944 | 1657/2682 | 553/893 | chr12 | 49599983 | |||
| chr12:49600048 | T | A | 1 | a0016 | 1 | NA18982.hp2 | missense_variant | MODERATE | c.1592A>T | p.Gln531Leu | FAM186B | ENSG00000135436.8 | transcript | ENST00000257894.2 | protein_coding | 4/7 | 1754/2944 | 1592/2682 | 531/893 | chr12 | 49600048 | |||
| chr12:49600183 | C | T | 1 | a0015 | 1 | NA18952.hp2 | missense_variant | MODERATE | c.1457G>A | p.Arg486Gln | FAM186B | ENSG00000135436.8 | transcript | ENST00000257894.2 | protein_coding | 4/7 | 1619/2944 | 1457/2682 | 486/893 | chr12 | 49600183 | |||
| chr12:49600279 | T | TGGAGTCC others(12): Show |
1 | a0010 | 1 | HG01168.hp2 | frameshift_variant | HIGH | c.1342_1360dupTTCCAG others(13): Show |
p.Gln454fs | FAM186B | ENSG00000135436.8 | transcript | ENST00000257894.2 | protein_coding | 4/7 | 1522/2944 | 1360/2682 | 454/893 | chr12 | 49600279 | |||
| chr12:49600448 | G | A | 2 | a0005 a0011 |
12 | HG01891.hp2 HG02109.hp2 HG02258.hp1 others(9): Show |
missense_variant | MODERATE | c.1192C>T | p.Arg398Cys | FAM186B | ENSG00000135436.8 | transcript | ENST00000257894.2 | protein_coding | 4/7 | 1354/2944 | 1192/2682 | 398/893 | chr12 | 49600448 | |||
| chr12:49600771 | C | G | 1 | a0011 | 1 | HG02258.hp1 | missense_variant | MODERATE | c.869G>C | p.Arg290Thr | FAM186B | ENSG00000135436.8 | transcript | ENST00000257894.2 | protein_coding | 4/7 | 1031/2944 | 869/2682 | 290/893 | chr12 | 49600771 | |||
| chr12:49600875 | C | G | 2 | a0004 a0012 |
13 | HG01109.hp1 HG01884.hp1 HG02145.hp2 others(10): Show |
missense_variant | MODERATE | c.765G>C | p.Arg255Ser | FAM186B | ENSG00000135436.8 | transcript | ENST00000257894.2 | protein_coding | 4/7 | 927/2944 | 765/2682 | 255/893 | chr12 | 49600875 | |||
| chr12:49601002 | G | A | 1 | a0009 | 2 | HG06807.hp2 NA19043.hp2 |
missense_variant | MODERATE | c.638C>T | p.Thr213Met | FAM186B | ENSG00000135436.8 | transcript | ENST00000257894.2 | protein_coding | 4/7 | 800/2944 | 638/2682 | 213/893 | chr12 | 49601002 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:49600359 | C | T | 1 | a0001c0014 | 1 | HG02451.hp2 | synonymous_variant | LOW | c.1281G>A | p.Lys427Lys | FAM186B | ENSG00000135436.8 | transcript | ENST00000257894.2 | protein_coding | 4/7 | 1443/2944 | 1281/2682 | 427/893 | chr12 | 49600359 | |||
| chr12:49600758 | C | T | 1 | a0006c0006 | 7 | HG01884.hp2 HG02055.hp2 HG02976.hp2 others(4): Show |
synonymous_variant | LOW | c.882G>A | p.Leu294Leu | FAM186B | ENSG00000135436.8 | transcript | ENST00000257894.2 | protein_coding | 4/7 | 1044/2944 | 882/2682 | 294/893 | chr12 | 49600758 | |||
| chr12:49605391 | C | T | 1 | a0001c0007 | 4 | HG01167.hp1 HG01169.hp1 HG02145.hp1 others(1): Show |
synonymous_variant | LOW | c.87G>A | p.Arg29Arg | FAM186B | ENSG00000135436.8 | transcript | ENST00000257894.2 | protein_coding | 1/7 | 249/2944 | 87/2682 | 29/893 | chr12 | 49605391 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:49587603 | G | T | 1 | a0001c0001t0003 | 5 | HG02056.hp2 NA18945.hp1 NA18990.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2C>A | FAM186B | ENSG00000135436.8 | transcript | ENST00000257894.2 | protein_coding | 7/7 | 2 | chr12 | 49587603 | ||||||
| chr12:49605492 | T | C | 2 | a0006c0006t0002 a0006c0010t0002 |
9 | HG01884.hp2 HG02055.hp2 HG02809.hp2 others(6): Show |
5_prime_UTR_variant | MODIFIER | c.-15A>G | FAM186B | ENSG00000135436.8 | transcript | ENST00000257894.2 | protein_coding | 1/7 | 15 | chr12 | 49605492 | ||||||
| chr12:49605619 | G | A | 1 | a0002c0002t0004 | 2 | HG02896.hp2 HG02897.hp1 |
5_prime_UTR_variant | MODIFIER | c.-142C>T | FAM186B | ENSG00000135436.8 | transcript | ENST00000257894.2 | protein_coding | 1/7 | 142 | chr12 | 49605619 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:49587939 | T | C | 32 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0013 others(29): Show |
69 | HG00280.hp2 HG00639.hp2 HG01106.hp1 others(66): Show |
intron_variant | MODIFIER | c.2535-187A>G | FAM186B | ENSG00000135436.8 | transcript | ENST00000257894.2 | protein_coding | 6/6 | chr12 | 49587939 | |||||||
| chr12:49587969 | G | A | 1 | a0014c0017t0001g0088 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.2535-217C>T | FAM186B | ENSG00000135436.8 | transcript | ENST00000257894.2 | protein_coding | 6/6 | chr12 | 49587969 | |||||||
| chr12:49588421 | C | T | 1 | a0004c0004t0001g0050 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2534+33G>A | FAM186B | ENSG00000135436.8 | transcript | ENST00000257894.2 | protein_coding | 6/6 | chr12 | 49588421 | |||||||
| chr12:49588728 | T | C | 1 | a0001c0001t0001g0072 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2365-105A>G | FAM186B | ENSG00000135436.8 | transcript | ENST00000257894.2 | protein_coding | 5/6 | chr12 | 49588728 | |||||||
| chr12:49588834 | G | C | 1 | a0001c0001t0001g0077 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2365-211C>G | FAM186B | ENSG00000135436.8 | transcript | ENST00000257894.2 | protein_coding | 5/6 | chr12 | 49588834 | |||||||
| chr12:49588862 | A | G | 1 | a0001c0001t0001g0076 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2365-239T>C | FAM186B | ENSG00000135436.8 | transcript | ENST00000257894.2 | protein_coding | 5/6 | chr12 | 49588862 | |||||||
| chr12:49588887 | G | A | 1 | a0001c0001t0001g0080 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2365-264C>T | FAM186B | ENSG00000135436.8 | transcript | ENST00000257894.2 | protein_coding | 5/6 | chr12 | 49588887 | |||||||
| chr12:49588888 | G | A | 1 | a0001c0001t0001g0073 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.2365-265C>T | FAM186B | ENSG00000135436.8 | transcript | ENST00000257894.2 | protein_coding | 5/6 | chr12 | 49588888 | |||||||
| chr12:49589098 | A | G | 1 | a0002c0002t0001g0055 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.2365-475T>C | FAM186B | ENSG00000135436.8 | transcript | ENST00000257894.2 | protein_coding | 5/6 | chr12 | 49589098 | |||||||
| chr12:49589173 | T | C | 1 | a0008c0009t0001g0078 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2365-550A>G | FAM186B | ENSG00000135436.8 | transcript | ENST00000257894.2 | protein_coding | 5/6 | chr12 | 49589173 | |||||||
| chr12:49589352 | C | T | 5 | a0006c0006t0002g0038 a0006c0006t0002g0039 a0006c0006t0002g0099 others(2): Show |
7 | HG01884.hp2 HG02055.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.2365-729G>A | FAM186B | ENSG00000135436.8 | transcript | ENST00000257894.2 | protein_coding | 5/6 | chr12 | 49589352 | |||||||
| chr12:49589595 | C | T | 37 | a0001c0001t0001g0016 a0001c0001t0001g0092 a0001c0001t0001g0093 others(34): Show |
77 | HG00280.hp2 HG00639.hp2 HG01106.hp1 others(74): Show |
intron_variant | MODIFIER | c.2365-972G>A | FAM186B | ENSG00000135436.8 | transcript | ENST00000257894.2 | protein_coding | 5/6 | chr12 | 49589595 | |||||||
| chr12:49589696 | A | G | 43 | a0001c0001t0001g0016 a0001c0001t0001g0092 a0001c0001t0001g0093 others(40): Show |
86 | HG00280.hp2 HG00639.hp2 HG01106.hp1 others(83): Show |
intron_variant | MODIFIER | c.2365-1073T>C | FAM186B | ENSG00000135436.8 | transcript | ENST00000257894.2 | protein_coding | 5/6 | chr12 | 49589696 | |||||||
| chr12:49589781 | G | A | 1 | a0016c0018t0001g0061 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.2365-1158C>T | FAM186B | ENSG00000135436.8 | transcript | ENST00000257894.2 | protein_coding | 5/6 | chr12 | 49589781 | |||||||
| chr12:49589840 | G | T | 2 | a0009c0011t0001g0042 a0009c0011t0001g0043 |
2 | HG06807.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2365-1217C>A | FAM186B | ENSG00000135436.8 | transcript | ENST00000257894.2 | protein_coding | 5/6 | chr12 | 49589840 | |||||||
| chr12:49589978 | C | CA | 46 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0010 others(43): Show |
100 | HG00280.hp1 HG00280.hp2 HG00621.hp1 others(97): Show |
intron_variant | MODIFIER | c.2365-1356dupT | FAM186B | ENSG00000135436.8 | transcript | ENST00000257894.2 | protein_coding | 5/6 | chr12 | 49589978 | |||||||
| chr12:49589978 | C | CAA | 8 | a0001c0001t0001g0040 a0002c0002t0001g0013 a0002c0002t0001g0014 others(5): Show |
15 | HG01175.hp1 HG02055.hp1 HG02293.hp1 others(12): Show |
intron_variant | MODIFIER | c.2365-1357_2365-135 others(6): Show |
FAM186B | ENSG00000135436.8 | transcript | ENST00000257894.2 | protein_coding | 5/6 | chr12 | 49589978 | |||||||
| chr12:49589978 | CA | C | 5 | a0001c0001t0001g0083 a0006c0006t0002g0038 a0006c0006t0002g0039 others(2): Show |
8 | HG01884.hp2 HG02055.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.2365-1356delT | FAM186B | ENSG00000135436.8 | transcript | ENST00000257894.2 | protein_coding | 5/6 | chr12 | 49589978 | |||||||
| chr12:49591047 | C | A | 1 | a0001c0001t0001g0074 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.2365-2424G>T | FAM186B | ENSG00000135436.8 | transcript | ENST00000257894.2 | protein_coding | 5/6 | chr12 | 49591047 | |||||||
| chr12:49591110 | T | A | 10 | a0003c0003t0001g0017 a0003c0003t0001g0030 a0005c0005t0001g0008 others(7): Show |
19 | HG01891.hp2 HG02109.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.2365-2487A>T | FAM186B | ENSG00000135436.8 | transcript | ENST00000257894.2 | protein_coding | 5/6 | chr12 | 49591110 | |||||||
| chr12:49591379 | T | A | 6 | a0002c0002t0001g0031 a0002c0002t0001g0041 a0002c0002t0001g0056 others(3): Show |
7 | HG01167.hp2 HG02486.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.2365-2756A>T | FAM186B | ENSG00000135436.8 | transcript | ENST00000257894.2 | protein_coding | 5/6 | chr12 | 49591379 | |||||||
| chr12:49591383 | T | C | 1 | a0001c0001t0001g0035 | 2 | HG02071.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.2365-2760A>G | FAM186B | ENSG00000135436.8 | transcript | ENST00000257894.2 | protein_coding | 5/6 | chr12 | 49591383 | |||||||
| chr12:49591427 | G | A | 43 | a0001c0001t0001g0016 a0001c0001t0001g0092 a0001c0001t0001g0093 others(40): Show |
86 | HG00280.hp2 HG00639.hp2 HG01106.hp1 others(83): Show |
intron_variant | MODIFIER | c.2365-2804C>T | FAM186B | ENSG00000135436.8 | transcript | ENST00000257894.2 | protein_coding | 5/6 | chr12 | 49591427 | |||||||
| chr12:49591583 | C | G | 1 | a0001c0001t0001g0071 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.2365-2960G>C | FAM186B | ENSG00000135436.8 | transcript | ENST00000257894.2 | protein_coding | 5/6 | chr12 | 49591583 | |||||||
| chr12:49591599 | T | C | 1 | a0001c0001t0001g0064 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2365-2976A>G | FAM186B | ENSG00000135436.8 | transcript | ENST00000257894.2 | protein_coding | 5/6 | chr12 | 49591599 | |||||||
| chr12:49591625 | G | A | 37 | a0001c0001t0001g0016 a0001c0001t0001g0092 a0001c0001t0001g0093 others(34): Show |
77 | HG00280.hp2 HG00639.hp2 HG01106.hp1 others(74): Show |
intron_variant | MODIFIER | c.2365-3002C>T | FAM186B | ENSG00000135436.8 | transcript | ENST00000257894.2 | protein_coding | 5/6 | chr12 | 49591625 | |||||||
| chr12:49591872 | ACTAT | A | 11 | a0002c0002t0001g0004 a0002c0002t0001g0013 a0002c0002t0001g0031 others(8): Show |
21 | HG00280.hp2 HG01167.hp2 HG02004.hp2 others(18): Show |
intron_variant | MODIFIER | c.2365-3253_2365-325 others(8): Show |
FAM186B | ENSG00000135436.8 | transcript | ENST00000257894.2 | protein_coding | 5/6 | chr12 | 49591872 | |||||||
| chr12:49592060 | A | G | 74 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0010 others(71): Show |
171 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.2365-3437T>C | FAM186B | ENSG00000135436.8 | transcript | ENST00000257894.2 | protein_coding | 5/6 | chr12 | 49592060 | |||||||
| chr12:49592092 | G | A | 1 | a0001c0001t0001g0044 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2365-3469C>T | FAM186B | ENSG00000135436.8 | transcript | ENST00000257894.2 | protein_coding | 5/6 | chr12 | 49592092 | |||||||
| chr12:49592100 | A | G | 2 | a0005c0005t0001g0032 a0011c0013t0001g0053 |
3 | HG02258.hp1 HG03098.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2365-3477T>C | FAM186B | ENSG00000135436.8 | transcript | ENST00000257894.2 | protein_coding | 5/6 | chr12 | 49592100 | |||||||
| chr12:49592270 | G | A | 4 | a0006c0006t0002g0038 a0006c0006t0002g0039 a0006c0006t0002g0099 others(1): Show |
6 | HG01884.hp2 HG02055.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.2365-3647C>T | FAM186B | ENSG00000135436.8 | transcript | ENST00000257894.2 | protein_coding | 5/6 | chr12 | 49592270 | |||||||
| chr12:49592689 | G | A | 1 | a0001c0001t0001g0022 | 3 | HG03490.hp2 HG03492.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.2365-4066C>T | FAM186B | ENSG00000135436.8 | transcript | ENST00000257894.2 | protein_coding | 5/6 | chr12 | 49592689 | |||||||
| chr12:49592699 | T | C | 2 | a0001c0001t0001g0092 a0001c0001t0001g0094 |
2 | HG02559.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2365-4076A>G | FAM186B | ENSG00000135436.8 | transcript | ENST00000257894.2 | protein_coding | 5/6 | chr12 | 49592699 | |||||||
| chr12:49592761 | A | G | 47 | a0001c0001t0001g0016 a0001c0001t0001g0064 a0001c0001t0001g0065 others(44): Show |
90 | HG00280.hp2 HG00639.hp2 HG01106.hp1 others(87): Show |
intron_variant | MODIFIER | c.2365-4138T>C | FAM186B | ENSG00000135436.8 | transcript | ENST00000257894.2 | protein_coding | 5/6 | chr12 | 49592761 | |||||||
| chr12:49592908 | A | G | 1 | a0001c0001t0001g0035 | 2 | HG02071.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.2365-4285T>C | FAM186B | ENSG00000135436.8 | transcript | ENST00000257894.2 | protein_coding | 5/6 | chr12 | 49592908 | |||||||
| chr12:49593139 | A | G | 4 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0089 others(1): Show |
4 | HG02451.hp2 HG04115.hp2 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.2365-4516T>C | FAM186B | ENSG00000135436.8 | transcript | ENST00000257894.2 | protein_coding | 5/6 | chr12 | 49593139 | |||||||
| chr12:49593506 | C | T | 2 | a0002c0002t0001g0031 a0002c0002t0001g0056 |
3 | HG01167.hp2 HG03516.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2365-4883G>A | FAM186B | ENSG00000135436.8 | transcript | ENST00000257894.2 | protein_coding | 5/6 | chr12 | 49593506 | |||||||
| chr12:49593632 | C | CAAAAA | 23 | a0002c0002t0001g0004 a0002c0002t0001g0013 a0002c0002t0001g0031 others(20): Show |
44 | HG00280.hp2 HG01167.hp2 HG01884.hp2 others(41): Show |
intron_variant | MODIFIER | c.2365-5014_2365-501 others(9): Show |
FAM186B | ENSG00000135436.8 | transcript | ENST00000257894.2 | protein_coding | 5/6 | chr12 | 49593632 | |||||||
| chr12:49593632 | C | CAAAAAA | 4 | a0001c0001t0001g0016 a0001c0001t0001g0093 a0009c0011t0001g0042 others(1): Show |
7 | HG01346.hp1 HG02257.hp1 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.2365-5015_2365-501 others(10): Show |
FAM186B | ENSG00000135436.8 | transcript | ENST00000257894.2 | protein_coding | 5/6 | chr12 | 49593632 | |||||||
| chr12:49593643 | A | AAAAAAG | 11 | a0002c0002t0001g0003 a0002c0002t0001g0014 a0002c0002t0001g0018 others(8): Show |
29 | HG00639.hp2 HG01106.hp1 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.2365-5021_2365-502 others(10): Show |
FAM186B | ENSG00000135436.8 | transcript | ENST00000257894.2 | protein_coding | 5/6 | chr12 | 49593643 | |||||||
| chr12:49593647 | G | A | 1 | a0006c0010t0002g0037 | 2 | HG02809.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.2365-5024C>T | FAM186B | ENSG00000135436.8 | transcript | ENST00000257894.2 | protein_coding | 5/6 | chr12 | 49593647 | |||||||
| chr12:49594023 | G | A | 3 | a0001c0001t0001g0005 a0001c0001t0001g0023 a0001c0001t0001g0095 |
11 | HG00735.hp2 HG00738.hp2 HG01081.hp2 others(8): Show |
intron_variant | MODIFIER | c.2364+4732C>T | FAM186B | ENSG00000135436.8 | transcript | ENST00000257894.2 | protein_coding | 5/6 | chr12 | 49594023 | |||||||
| chr12:49594146 | G | A | 55 | a0001c0001t0001g0006 a0001c0001t0001g0016 a0001c0001t0001g0021 others(52): Show |
110 | HG00280.hp1 HG00280.hp2 HG00639.hp2 others(107): Show |
intron_variant | MODIFIER | c.2364+4609C>T | FAM186B | ENSG00000135436.8 | transcript | ENST00000257894.2 | protein_coding | 5/6 | chr12 | 49594146 | |||||||
| chr12:49594152 | A | G | 1 | a0001c0001t0001g0075 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2364+4603T>C | FAM186B | ENSG00000135436.8 | transcript | ENST00000257894.2 | protein_coding | 5/6 | chr12 | 49594152 | |||||||
| chr12:49594308 | T | A | 1 | a0001c0001t0001g0081 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.2364+4447A>T | FAM186B | ENSG00000135436.8 | transcript | ENST00000257894.2 | protein_coding | 5/6 | chr12 | 49594308 | |||||||
| chr12:49594524 | T | G | 74 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0010 others(71): Show |
171 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.2364+4231A>C | FAM186B | ENSG00000135436.8 | transcript | ENST00000257894.2 | protein_coding | 5/6 | chr12 | 49594524 | |||||||
| chr12:49594548 | T | G | 1 | a0001c0001t0003g0082 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.2364+4207A>C | FAM186B | ENSG00000135436.8 | transcript | ENST00000257894.2 | protein_coding | 5/6 | chr12 | 49594548 | |||||||
| chr12:49594827 | A | C | 1 | a0001c0001t0001g0021 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.2364+3928T>G | FAM186B | ENSG00000135436.8 | transcript | ENST00000257894.2 | protein_coding | 5/6 | chr12 | 49594827 | |||||||
| chr12:49594874 | CA | C | 10 | a0001c0001t0001g0016 a0001c0001t0001g0092 a0001c0001t0001g0093 others(7): Show |
16 | HG01346.hp1 HG01884.hp2 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.2364+3880delT | FAM186B | ENSG00000135436.8 | transcript | ENST00000257894.2 | protein_coding | 5/6 | chr12 | 49594874 | |||||||
| chr12:49595176 | C | T | 1 | a0001c0001t0001g0070 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2364+3579G>A | FAM186B | ENSG00000135436.8 | transcript | ENST00000257894.2 | protein_coding | 5/6 | chr12 | 49595176 | |||||||
| chr12:49595322 | A | T | 12 | a0002c0002t0001g0003 a0002c0002t0001g0014 a0002c0002t0001g0018 others(9): Show |
30 | HG00639.hp2 HG01106.hp1 HG01106.hp2 others(27): Show |
intron_variant | MODIFIER | c.2364+3433T>A | FAM186B | ENSG00000135436.8 | transcript | ENST00000257894.2 | protein_coding | 5/6 | chr12 | 49595322 | |||||||
| chr12:49595553 | G | A | 23 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0013 others(20): Show |
51 | HG00280.hp2 HG00639.hp2 HG01106.hp1 others(48): Show |
intron_variant | MODIFIER | c.2364+3202C>T | FAM186B | ENSG00000135436.8 | transcript | ENST00000257894.2 | protein_coding | 5/6 | chr12 | 49595553 | |||||||
| chr12:49595820 | A | G | 6 | a0006c0006t0002g0038 a0006c0006t0002g0039 a0006c0006t0002g0099 others(3): Show |
9 | HG01884.hp2 HG02055.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.2364+2935T>C | FAM186B | ENSG00000135436.8 | transcript | ENST00000257894.2 | protein_coding | 5/6 | chr12 | 49595820 | |||||||
| chr12:49595928 | G | A | 1 | a0001c0001t0001g0024 | 3 | NA18963.hp2 NA18966.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.2364+2827C>T | FAM186B | ENSG00000135436.8 | transcript | ENST00000257894.2 | protein_coding | 5/6 | chr12 | 49595928 | |||||||
| chr12:49595963 | G | A | 1 | a0002c0002t0001g0059 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.2364+2792C>T | FAM186B | ENSG00000135436.8 | transcript | ENST00000257894.2 | protein_coding | 5/6 | chr12 | 49595963 | |||||||
| chr12:49595963 | G | C | 5 | a0006c0006t0002g0038 a0006c0006t0002g0039 a0006c0006t0002g0100 others(2): Show |
8 | HG01884.hp2 HG02055.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.2364+2792C>G | FAM186B | ENSG00000135436.8 | transcript | ENST00000257894.2 | protein_coding | 5/6 | chr12 | 49595963 | |||||||
| chr12:49596050 | C | T | 1 | a0001c0001t0001g0047 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2364+2705G>A | FAM186B | ENSG00000135436.8 | transcript | ENST00000257894.2 | protein_coding | 5/6 | chr12 | 49596050 | |||||||
| chr12:49596299 | G | A | 6 | a0006c0006t0002g0038 a0006c0006t0002g0039 a0006c0006t0002g0099 others(3): Show |
9 | HG01884.hp2 HG02055.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.2364+2456C>T | FAM186B | ENSG00000135436.8 | transcript | ENST00000257894.2 | protein_coding | 5/6 | chr12 | 49596299 | |||||||
| chr12:49596323 | C | CA | 36 | a0001c0001t0001g0011 a0001c0001t0001g0025 a0001c0001t0001g0046 others(33): Show |
77 | HG00140.hp1 HG00280.hp2 HG01106.hp1 others(74): Show |
intron_variant | MODIFIER | c.2364+2431dupT | FAM186B | ENSG00000135436.8 | transcript | ENST00000257894.2 | protein_coding | 5/6 | chr12 | 49596323 | |||||||
| chr12:49596323 | C | CAA | 6 | a0001c0001t0001g0016 a0001c0001t0001g0085 a0001c0001t0001g0092 others(3): Show |
11 | HG00639.hp2 HG01106.hp2 HG01192.hp1 others(8): Show |
intron_variant | MODIFIER | c.2364+2430_2364+243 others(6): Show |
FAM186B | ENSG00000135436.8 | transcript | ENST00000257894.2 | protein_coding | 5/6 | chr12 | 49596323 | |||||||
| chr12:49596323 | CA | C | 10 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0086 others(7): Show |
16 | HG00423.hp2 HG01884.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.2364+2431delT | FAM186B | ENSG00000135436.8 | transcript | ENST00000257894.2 | protein_coding | 5/6 | chr12 | 49596323 | |||||||
| chr12:49596485 | T | TA | 22 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0002c0002t0001g0003 others(19): Show |
45 | HG00280.hp2 HG00639.hp2 HG00741.hp1 others(42): Show |
intron_variant | MODIFIER | c.2364+2269dupT | FAM186B | ENSG00000135436.8 | transcript | ENST00000257894.2 | protein_coding | 5/6 | chr12 | 49596485 | |||||||
| chr12:49596485 | T | TAA | 3 | a0004c0004t0001g0007 a0004c0004t0001g0045 a0004c0004t0001g0052 |
8 | HG01884.hp1 HG02630.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.2364+2268_2364+226 others(6): Show |
FAM186B | ENSG00000135436.8 | transcript | ENST00000257894.2 | protein_coding | 5/6 | chr12 | 49596485 | |||||||
| chr12:49597204 | T | C | 6 | a0002c0002t0001g0031 a0002c0002t0001g0041 a0002c0002t0001g0056 others(3): Show |
7 | HG01167.hp2 HG02486.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.2364+1551A>G | FAM186B | ENSG00000135436.8 | transcript | ENST00000257894.2 | protein_coding | 5/6 | chr12 | 49597204 | |||||||
| chr12:49597588 | C | T | 6 | a0006c0006t0002g0038 a0006c0006t0002g0039 a0006c0006t0002g0099 others(3): Show |
9 | HG01884.hp2 HG02055.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.2364+1167G>A | FAM186B | ENSG00000135436.8 | transcript | ENST00000257894.2 | protein_coding | 5/6 | chr12 | 49597588 | |||||||
| chr12:49598022 | C | T | 11 | a0002c0002t0001g0004 a0002c0002t0001g0013 a0002c0002t0001g0031 others(8): Show |
21 | HG00280.hp2 HG01167.hp2 HG02004.hp2 others(18): Show |
intron_variant | MODIFIER | c.2364+733G>A | FAM186B | ENSG00000135436.8 | transcript | ENST00000257894.2 | protein_coding | 5/6 | chr12 | 49598022 | |||||||
| chr12:49598147 | G | T | 1 | a0001c0001t0001g0093 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2364+608C>A | FAM186B | ENSG00000135436.8 | transcript | ENST00000257894.2 | protein_coding | 5/6 | chr12 | 49598147 | |||||||
| chr12:49598500 | T | C | 1 | a0001c0001t0001g0016 | 4 | HG01346.hp1 HG02257.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.2364+255A>G | FAM186B | ENSG00000135436.8 | transcript | ENST00000257894.2 | protein_coding | 5/6 | chr12 | 49598500 | |||||||
| chr12:49599367 | C | G | 4 | a0006c0006t0002g0038 a0006c0006t0002g0039 a0006c0006t0002g0099 others(1): Show |
6 | HG01884.hp2 HG02055.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.2171+102G>C | FAM186B | ENSG00000135436.8 | transcript | ENST00000257894.2 | protein_coding | 4/6 | chr12 | 49599367 | |||||||
| chr12:49599389 | T | C | 4 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0089 others(1): Show |
4 | HG02451.hp2 HG04115.hp2 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.2171+80A>G | FAM186B | ENSG00000135436.8 | transcript | ENST00000257894.2 | protein_coding | 4/6 | chr12 | 49599389 | |||||||
| chr12:49601333 | C | T | 1 | a0001c0001t0001g0064 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.506-199G>A | FAM186B | ENSG00000135436.8 | transcript | ENST00000257894.2 | protein_coding | 3/6 | chr12 | 49601333 | |||||||
| chr12:49601429 | A | G | 2 | a0001c0001t0001g0064 a0001c0001t0001g0065 |
2 | HG04115.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.506-295T>C | FAM186B | ENSG00000135436.8 | transcript | ENST00000257894.2 | protein_coding | 3/6 | chr12 | 49601429 | |||||||
| chr12:49601621 | G | GT | 33 | a0001c0001t0001g0060 a0002c0002t0001g0003 a0002c0002t0001g0004 others(30): Show |
70 | HG00280.hp2 HG00639.hp2 HG01106.hp1 others(67): Show |
intron_variant | MODIFIER | c.506-488dupA | FAM186B | ENSG00000135436.8 | transcript | ENST00000257894.2 | protein_coding | 3/6 | chr12 | 49601621 | |||||||
| chr12:49601621 | G | GTT | 4 | a0001c0001t0001g0016 a0001c0001t0001g0092 a0001c0001t0001g0093 others(1): Show |
7 | HG01346.hp1 HG02257.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.506-489_506-488dup others(2): Show |
FAM186B | ENSG00000135436.8 | transcript | ENST00000257894.2 | protein_coding | 3/6 | chr12 | 49601621 | |||||||
| chr12:49601675 | C | T | 1 | a0001c0001t0001g0048 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.506-541G>A | FAM186B | ENSG00000135436.8 | transcript | ENST00000257894.2 | protein_coding | 3/6 | chr12 | 49601675 | |||||||
| chr12:49601698 | C | T | 1 | a0001c0001t0001g0047 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.506-564G>A | FAM186B | ENSG00000135436.8 | transcript | ENST00000257894.2 | protein_coding | 3/6 | chr12 | 49601698 | |||||||
| chr12:49601763 | G | T | 1 | a0001c0001t0001g0092 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.506-629C>A | FAM186B | ENSG00000135436.8 | transcript | ENST00000257894.2 | protein_coding | 3/6 | chr12 | 49601763 | |||||||
| chr12:49602343 | T | C | 4 | a0001c0001t0001g0016 a0001c0001t0001g0092 a0001c0001t0001g0093 others(1): Show |
7 | HG01346.hp1 HG02257.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.505+842A>G | FAM186B | ENSG00000135436.8 | transcript | ENST00000257894.2 | protein_coding | 3/6 | chr12 | 49602343 | |||||||
| chr12:49602393 | A | G | 1 | a0001c0001t0001g0046 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.505+792T>C | FAM186B | ENSG00000135436.8 | transcript | ENST00000257894.2 | protein_coding | 3/6 | chr12 | 49602393 | |||||||
| chr12:49602539 | G | A | 1 | a0001c0001t0001g0036 | 2 | NA18984.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.505+646C>T | FAM186B | ENSG00000135436.8 | transcript | ENST00000257894.2 | protein_coding | 3/6 | chr12 | 49602539 | |||||||
| chr12:49602590 | G | A | 1 | a0004c0004t0001g0045 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.505+595C>T | FAM186B | ENSG00000135436.8 | transcript | ENST00000257894.2 | protein_coding | 3/6 | chr12 | 49602590 | |||||||
| chr12:49602665 | C | G | 102 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(99): Show |
262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.505+520G>C | FAM186B | ENSG00000135436.8 | transcript | ENST00000257894.2 | protein_coding | 3/6 | chr12 | 49602665 | |||||||
| chr12:49602702 | C | T | 2 | a0007c0008t0001g0028 a0007c0008t0001g0096 |
3 | HG00423.hp1 NA18981.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.505+483G>A | FAM186B | ENSG00000135436.8 | transcript | ENST00000257894.2 | protein_coding | 3/6 | chr12 | 49602702 | |||||||
| chr12:49602718 | G | A | 1 | a0001c0001t0001g0095 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.505+467C>T | FAM186B | ENSG00000135436.8 | transcript | ENST00000257894.2 | protein_coding | 3/6 | chr12 | 49602718 | |||||||
| chr12:49602891 | C | G | 2 | a0004c0004t0001g0007 a0004c0004t0001g0045 |
7 | HG01884.hp1 HG02630.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.505+294G>C | FAM186B | ENSG00000135436.8 | transcript | ENST00000257894.2 | protein_coding | 3/6 | chr12 | 49602891 | |||||||
| chr12:49602892 | C | T | 1 | a0001c0001t0001g0044 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.505+293G>A | FAM186B | ENSG00000135436.8 | transcript | ENST00000257894.2 | protein_coding | 3/6 | chr12 | 49602892 | |||||||
| chr12:49603002 | C | T | 2 | a0009c0011t0001g0042 a0009c0011t0001g0043 |
2 | HG06807.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.505+183G>A | FAM186B | ENSG00000135436.8 | transcript | ENST00000257894.2 | protein_coding | 3/6 | chr12 | 49603002 | |||||||
| chr12:49603522 | G | A | 1 | a0007c0008t0001g0096 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.323-155C>T | FAM186B | ENSG00000135436.8 | transcript | ENST00000257894.2 | protein_coding | 2/6 | chr12 | 49603522 | |||||||
| chr12:49603603 | C | T | 1 | a0002c0002t0001g0041 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.323-236G>A | FAM186B | ENSG00000135436.8 | transcript | ENST00000257894.2 | protein_coding | 2/6 | chr12 | 49603603 | |||||||
| chr12:49603695 | A | G | 2 | a0001c0001t0001g0027 a0001c0001t0001g0040 |
3 | HG01943.hp1 HG02293.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.323-328T>C | FAM186B | ENSG00000135436.8 | transcript | ENST00000257894.2 | protein_coding | 2/6 | chr12 | 49603695 | |||||||
| chr12:49604260 | G | A | 1 | a0001c0001t0001g0097 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.322+53C>T | FAM186B | ENSG00000135436.8 | transcript | ENST00000257894.2 | protein_coding | 2/6 | chr12 | 49604260 | |||||||
| chr12:49605010 | C | T | 1 | a0006c0010t0002g0037 | 2 | HG02809.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.96+372G>A | FAM186B | ENSG00000135436.8 | transcript | ENST00000257894.2 | protein_coding | 1/6 | chr12 | 49605010 | |||||||
| chr12:49605231 | A | G | 1 | a0003c0003t0001g0017 | 3 | HG02647.hp1 HG02723.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.96+151T>C | FAM186B | ENSG00000135436.8 | transcript | ENST00000257894.2 | protein_coding | 1/6 | chr12 | 49605231 | |||||||
| chr12:49605336 | G | A | 1 | a0001c0001t0001g0098 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.96+46C>T | FAM186B | ENSG00000135436.8 | transcript | ENST00000257894.2 | protein_coding | 1/6 | chr12 | 49605336 |