Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 143684 |
| ensemblid | ENSG00000077458.13 |
| hgncid | 28492 |
| symbol | FAM76B |
| name | family with sequence similarity 76 member B |
| refseq_nuc | NM_144664.5 |
| refseq_prot | NP_653265.3 |
| ensembl_nuc | ENST00000358780.10 |
| ensembl_prot | ENSP00000351631.5 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 95768953 |
| end | 95789782 |
| strand | - |
| ver | v1.2 |
| region | chr11:95768953-95789782 |
| region5000 | chr11:95763953-95794782 |
| regionname0 | FAM76B_chr11_95768953_95789782 |
| regionname5000 | FAM76B_chr11_95763953_95794782 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1020 | 243 | 91 | 36 | 79 | 9 | 27 | FAM76B_chr11_95763953_95794782 | FAM76B | ATGGC others(1015): Show |
chr11 | 95763953 | 95794782 | ||
| a0001c0002 | 1/0 | 1020 | 166 | 5 | 39 | 97 | 5 | 19 | FAM76B_chr11_95763953_95794782 | FAM76B | ATGGC others(1015): Show |
chr11 | 95763953 | 95794782 | ||
| a0001c0003 | 0/0 | 1020 | 3 | 3 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | ATGGC others(1015): Show |
chr11 | 95763953 | 95794782 | ||
| a0001c0004 | 0/0 | 1020 | 2 | 0 | 0 | 2 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | ATGGC others(1015): Show |
chr11 | 95763953 | 95794782 | ||
| a0001c0005 | 0/0 | 1020 | 2 | 1 | 1 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | ATGGC others(1015): Show |
chr11 | 95763953 | 95794782 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3932 | 111 | 69 | 17 | 18 | 1 | 6 | FAM76B_chr11_95763953_95794782 | FAM76B | GGATC others(3927): Show |
chr11 | 95763953 | 95794782 |
| a0001c0001t0002 | 0/0 | 3932 | 88 | 6 | 15 | 52 | 8 | 7 | FAM76B_chr11_95763953_95794782 | FAM76B | GGATC others(3927): Show |
chr11 | 95763953 | 95794782 |
| a0001c0001t0003 | 0/0 | 3929 | 15 | 7 | 1 | 0 | 0 | 7 | FAM76B_chr11_95763953_95794782 | FAM76B | GGATC others(3924): Show |
chr11 | 95763953 | 95794782 |
| a0001c0001t0004 | 0/1 | 3932 | 7 | 0 | 0 | 0 | 0 | 6 | FAM76B_chr11_95763953_95794782 | FAM76B | GGATC others(3927): Show |
chr11 | 95763953 | 95794782 |
| a0001c0001t0005 | 0/0 | 3932 | 3 | 3 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | GGATC others(3927): Show |
chr11 | 95763953 | 95794782 |
| a0001c0001t0007 | 0/0 | 3932 | 3 | 0 | 0 | 3 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | GGATC others(3927): Show |
chr11 | 95763953 | 95794782 |
| a0001c0001t0008 | 0/0 | 3932 | 3 | 2 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | GGATC others(3927): Show |
chr11 | 95763953 | 95794782 |
| a0001c0001t0010 | 0/0 | 3932 | 2 | 0 | 2 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | GGATC others(3927): Show |
chr11 | 95763953 | 95794782 |
| a0001c0001t0011 | 0/0 | 3932 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | GGATC others(3927): Show |
chr11 | 95763953 | 95794782 |
| a0001c0001t0013 | 0/0 | 3932 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | GGATC others(3927): Show |
chr11 | 95763953 | 95794782 |
| a0001c0001t0015 | 0/0 | 3932 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | GGATC others(3927): Show |
chr11 | 95763953 | 95794782 |
| a0001c0001t0016 | 0/0 | 3932 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | GGATC others(3927): Show |
chr11 | 95763953 | 95794782 |
| a0001c0001t0018 | 0/0 | 3932 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | GGATC others(3927): Show |
chr11 | 95763953 | 95794782 |
| a0001c0001t0019 | 0/0 | 3932 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | GGATC others(3927): Show |
chr11 | 95763953 | 95794782 |
| a0001c0001t0020 | 0/0 | 3953 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | GGATC others(3948): Show |
chr11 | 95763953 | 95794782 |
| a0001c0001t0021 | 0/0 | 3932 | 1 | 0 | 0 | 0 | 0 | 1 | FAM76B_chr11_95763953_95794782 | FAM76B | GGATC others(3927): Show |
chr11 | 95763953 | 95794782 |
| a0001c0001t0022 | 0/0 | 3932 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | GGATC others(3927): Show |
chr11 | 95763953 | 95794782 |
| a0001c0001t0023 | 0/0 | 3932 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | GGATC others(3927): Show |
chr11 | 95763953 | 95794782 |
| a0001c0001t0024 | 0/0 | 3932 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | GGATC others(3927): Show |
chr11 | 95763953 | 95794782 |
| a0001c0002t0001 | 1/0 | 3932 | 158 | 4 | 35 | 94 | 5 | 19 | FAM76B_chr11_95763953_95794782 | FAM76B | GGATC others(3927): Show |
chr11 | 95763953 | 95794782 |
| a0001c0002t0006 | 0/0 | 3932 | 3 | 0 | 3 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | GGATC others(3927): Show |
chr11 | 95763953 | 95794782 |
| a0001c0002t0009 | 0/0 | 3932 | 2 | 0 | 0 | 2 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | GGATC others(3927): Show |
chr11 | 95763953 | 95794782 |
| a0001c0002t0012 | 0/0 | 3932 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | GGATC others(3927): Show |
chr11 | 95763953 | 95794782 |
| a0001c0002t0014 | 0/0 | 3932 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | GGATC others(3927): Show |
chr11 | 95763953 | 95794782 |
| a0001c0002t0017 | 0/0 | 3932 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | GGATC others(3927): Show |
chr11 | 95763953 | 95794782 |
| a0001c0003t0001 | 0/0 | 3932 | 3 | 3 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | GGATC others(3927): Show |
chr11 | 95763953 | 95794782 |
| a0001c0004t0001 | 0/0 | 3932 | 2 | 0 | 0 | 2 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | GGATC others(3927): Show |
chr11 | 95763953 | 95794782 |
| a0001c0005t0001 | 0/0 | 3932 | 2 | 1 | 1 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | GGATC others(3927): Show |
chr11 | 95763953 | 95794782 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0007 | 0/0 | 12 | 10 | 2 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0001t0001g0009 | 0/0 | 8 | 7 | 1 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0001t0001g0010 | 0/0 | 8 | 1 | 0 | 6 | 0 | 1 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0001t0001g0011 | 0/0 | 7 | 6 | 1 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0001t0001g0013 | 0/0 | 6 | 0 | 0 | 4 | 0 | 2 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0001t0001g0016 | 0/0 | 5 | 3 | 2 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0001t0001g0017 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0001t0001g0018 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0001t0001g0019 | 0/0 | 4 | 1 | 3 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0001t0001g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0001t0001g0022 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0001t0001g0023 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0001t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0001t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0001t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0001t0001g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0001t0002g0001 | 0/0 | 56 | 3 | 10 | 36 | 5 | 2 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0001t0002g0012 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0001t0002g0027 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0001t0002g0028 | 0/0 | 3 | 1 | 1 | 0 | 0 | 1 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0001t0002g0042 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0001t0002g0043 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0001t0002g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0001t0003g0008 | 0/0 | 8 | 4 | 0 | 0 | 0 | 4 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0001t0003g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0001t0003g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0001t0003g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0001t0003g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0001t0003g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0001t0003g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0001t0004g0015 | 0/1 | 5 | 0 | 0 | 0 | 0 | 4 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0001t0004g0029 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0001t0005g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0001t0007g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0001t0007g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0001t0008g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0001t0008g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0001t0010g0046 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0001t0011g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0001t0013g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0001t0015g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0001t0016g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0001t0018g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0001t0019g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0001t0020g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0001t0021g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0001t0022g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0001t0023g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0001t0024g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0002t0001g0002 | 0/0 | 30 | 1 | 1 | 22 | 1 | 5 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0002t0001g0003 | 0/0 | 28 | 0 | 6 | 21 | 0 | 1 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0002t0001g0004 | 0/0 | 19 | 0 | 3 | 14 | 0 | 2 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0002t0001g0005 | 0/0 | 14 | 1 | 8 | 2 | 0 | 3 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0002t0001g0006 | 0/0 | 13 | 0 | 4 | 9 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0002t0001g0014 | 0/0 | 6 | 0 | 5 | 0 | 1 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0002t0001g0025 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0002t0001g0026 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0002t0001g0035 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0002t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0002t0001g0037 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0002t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0002t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0002t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0002t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0002t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0002t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0002t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0002t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0002t0001g0112 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0002t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0002t0006g0024 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0002t0009g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0002t0012g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0002t0014g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0002t0017g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0003t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0003t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0003t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0004t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| a0001c0005t0001g0038 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0001 | g0111 | EUR | GBR | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0001 | EUR | GBR | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0027 | EUR | GBR | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0001 | EUR | GBR | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG00280 | hp1 | a0001 | c0002 | t0001 | g0002 | EUR | FIN | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0151 | EUR | FIN | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0001 | EUR | FIN | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0080 | EUR | FIN | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG00408 | hp1 | a0001 | c0002 | t0001 | g0115 | EAS | CHS | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | CHS | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG00423 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | CHS | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0043 | EAS | CHS | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG00438 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | CHS | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG00544 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | CHS | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | CHS | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG00558 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | CHS | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG00597 | hp1 | a0001 | c0002 | t0001 | g0006 | EAS | CHS | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG00609 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | CHS | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG00621 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | CHS | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG00621 | hp2 | a0001 | c0002 | t0001 | g0106 | EAS | CHS | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG00639 | hp2 | a0001 | c0001 | t0010 | g0046 | AMR | PUR | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG00642 | hp1 | a0001 | c0002 | t0001 | g0003 | AMR | PUR | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG00642 | hp2 | a0001 | c0002 | t0001 | g0014 | AMR | PUR | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG00673 | hp1 | a0001 | c0002 | t0001 | g0102 | EAS | CHS | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG00673 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | CHS | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0154 | AMR | PUR | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG00735 | hp1 | a0001 | c0002 | t0001 | g0003 | AMR | PUR | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG00735 | hp2 | a0001 | c0002 | t0001 | g0014 | AMR | PUR | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG00738 | hp1 | a0001 | c0002 | t0001 | g0089 | AMR | PUR | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0027 | AMR | PUR | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG01069 | hp1 | a0001 | c0001 | t0010 | g0046 | AMR | PUR | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG01069 | hp2 | a0001 | c0002 | t0006 | g0024 | AMR | PUR | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG01071 | hp1 | a0001 | c0002 | t0006 | g0024 | AMR | PUR | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG01074 | hp2 | a0001 | c0002 | t0006 | g0024 | AMR | PUR | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG01081 | hp2 | a0001 | c0002 | t0001 | g0095 | AMR | PUR | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG01099 | hp2 | a0001 | c0002 | t0001 | g0005 | AMR | PUR | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG01109 | hp1 | a0001 | c0002 | t0001 | g0014 | AMR | PUR | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG01167 | hp2 | a0001 | c0002 | t0001 | g0003 | AMR | PUR | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0042 | AMR | PUR | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0042 | AMR | PUR | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG01175 | hp1 | a0001 | c0002 | t0001 | g0005 | AMR | PUR | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG01192 | hp2 | a0001 | c0002 | t0001 | g0003 | AMR | PUR | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG01255 | hp1 | a0001 | c0002 | t0001 | g0101 | AMR | CLM | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG01255 | hp2 | a0001 | c0002 | t0001 | g0124 | AMR | CLM | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG01256 | hp1 | a0001 | c0002 | t0001 | g0006 | AMR | CLM | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0028 | AMR | CLM | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG01257 | hp2 | a0001 | c0002 | t0001 | g0005 | AMR | CLM | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG01258 | hp2 | a0001 | c0002 | t0001 | g0005 | AMR | CLM | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG01261 | hp1 | a0001 | c0002 | t0001 | g0004 | AMR | CLM | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG01346 | hp1 | a0001 | c0005 | t0001 | g0038 | AMR | CLM | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG01346 | hp2 | a0001 | c0002 | t0001 | g0107 | AMR | CLM | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG01358 | hp1 | a0001 | c0002 | t0001 | g0005 | AMR | CLM | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG01358 | hp2 | a0001 | c0002 | t0014 | g0092 | AMR | CLM | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG01433 | hp1 | a0001 | c0002 | t0001 | g0003 | AMR | CLM | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG01433 | hp2 | a0001 | c0002 | t0001 | g0093 | AMR | CLM | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG01496 | hp1 | a0001 | c0002 | t0001 | g0004 | AMR | CLM | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG01496 | hp2 | a0001 | c0002 | t0001 | g0014 | AMR | CLM | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0153 | EUR | IBS | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG01516 | hp2 | a0001 | c0002 | t0001 | g0088 | EUR | IBS | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0001 | AFR | ACB | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | ACB | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | ACB | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PEL | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG01928 | hp2 | a0001 | c0002 | t0001 | g0003 | AMR | PEL | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG01952 | hp1 | a0001 | c0002 | t0001 | g0004 | AMR | PEL | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG01952 | hp2 | a0001 | c0002 | t0001 | g0006 | AMR | PEL | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG01975 | hp1 | a0001 | c0002 | t0001 | g0006 | AMR | PEL | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PEL | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG01978 | hp1 | a0001 | c0001 | t0013 | g0070 | AMR | PEL | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG01978 | hp2 | a0001 | c0002 | t0001 | g0005 | AMR | PEL | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG01981 | hp1 | a0001 | c0002 | t0001 | g0094 | AMR | PEL | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG01981 | hp2 | a0001 | c0002 | t0001 | g0006 | AMR | PEL | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG01993 | hp1 | a0001 | c0002 | t0001 | g0005 | AMR | PEL | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG01993 | hp2 | a0001 | c0002 | t0001 | g0097 | AMR | PEL | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | PEL | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PEL | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG02015 | hp1 | a0001 | c0002 | t0009 | g0034 | EAS | KHV | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG02015 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | KHV | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG02027 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | KHV | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG02027 | hp2 | a0001 | c0002 | t0001 | g0104 | EAS | KHV | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG02040 | hp2 | a0001 | c0002 | t0001 | g0006 | EAS | KHV | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | ACB | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG02055 | hp2 | a0001 | c0002 | t0001 | g0103 | AFR | ACB | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG02056 | hp1 | a0001 | c0001 | t0024 | g0155 | EAS | KHV | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG02071 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | KHV | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG02074 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | KHV | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG02074 | hp2 | a0001 | c0002 | t0009 | g0034 | EAS | KHV | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | KHV | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG02080 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | KHV | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG02129 | hp1 | a0001 | c0002 | t0001 | g0026 | EAS | KHV | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG02129 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | KHV | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG02132 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | KHV | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG02132 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | KHV | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG02135 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | KHV | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0028 | AFR | ACB | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | ACB | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG02148 | hp1 | a0001 | c0002 | t0001 | g0005 | AMR | PEL | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG02155 | hp1 | a0001 | c0002 | t0001 | g0087 | EAS | CDX | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG02155 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | CDX | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG02165 | hp1 | a0001 | c0002 | t0001 | g0110 | EAS | CDX | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG02165 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | CDX | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG02257 | hp1 | a0001 | c0002 | t0001 | g0002 | AFR | ACB | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | ACB | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG02258 | hp2 | a0001 | c0002 | t0012 | g0048 | AFR | ACB | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | ACB | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG02300 | hp1 | a0001 | c0001 | t0003 | g0052 | AMR | PEL | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG02300 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | PEL | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | GWD | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG02602 | hp2 | a0001 | c0002 | t0001 | g0003 | SAS | PJL | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | GWD | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | GWD | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | GWD | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG02647 | hp1 | a0001 | c0001 | t0003 | g0008 | AFR | GWD | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | GWD | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG02683 | hp1 | a0001 | c0002 | t0001 | g0090 | SAS | PJL | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG02683 | hp2 | a0001 | c0002 | t0001 | g0025 | SAS | PJL | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG02698 | hp1 | a0001 | c0002 | t0001 | g0099 | SAS | PJL | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0138 | SAS | PJL | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG02717 | hp1 | a0001 | c0005 | t0001 | g0038 | AFR | GWD | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0027 | SAS | PJL | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG02735 | hp2 | a0001 | c0001 | t0003 | g0059 | SAS | PJL | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG02738 | hp1 | a0001 | c0002 | t0001 | g0002 | SAS | PJL | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG02738 | hp2 | a0001 | c0002 | t0001 | g0005 | SAS | PJL | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG02818 | hp1 | a0001 | c0001 | t0003 | g0058 | AFR | GWD | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | GWD | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG02895 | hp1 | a0001 | c0001 | t0003 | g0030 | AFR | GWD | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0001 | AFR | GWD | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG02897 | hp1 | a0001 | c0001 | t0003 | g0030 | AFR | GWD | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | ESN | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0077 | AFR | ESN | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | ESN | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG02965 | hp2 | a0001 | c0001 | t0003 | g0008 | AFR | ESN | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | ESN | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG02976 | hp1 | a0001 | c0001 | t0008 | g0045 | AFR | ESN | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG03041 | hp1 | a0001 | c0003 | t0001 | g0056 | AFR | GWD | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | GWD | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0147 | AFR | MSL | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | ESN | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0008 | AFR | ESN | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG03209 | hp1 | a0001 | c0001 | t0008 | g0045 | AFR | MSL | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG03209 | hp2 | a0001 | c0001 | t0018 | g0050 | AFR | MSL | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | MSL | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | MSL | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG03239 | hp1 | a0001 | c0001 | t0003 | g0060 | SAS | PJL | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG03239 | hp2 | a0001 | c0001 | t0004 | g0029 | SAS | PJL | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG03453 | hp1 | a0001 | c0001 | t0016 | g0049 | AFR | MSL | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | MSL | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | MSL | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | MSL | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG03490 | hp1 | a0001 | c0002 | t0001 | g0002 | SAS | PJL | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG03490 | hp2 | a0001 | c0001 | t0003 | g0008 | SAS | PJL | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG03491 | hp1 | a0001 | c0001 | t0004 | g0029 | SAS | PJL | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG03491 | hp2 | a0001 | c0002 | t0001 | g0005 | SAS | PJL | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG03492 | hp1 | a0001 | c0002 | t0001 | g0002 | SAS | PJL | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG03492 | hp2 | a0001 | c0002 | t0001 | g0005 | SAS | PJL | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | ESN | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG03516 | hp2 | a0001 | c0001 | t0011 | g0047 | AFR | ESN | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG03540 | hp1 | a0001 | c0001 | t0005 | g0020 | AFR | GWD | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | MSL | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0140 | SAS | PJL | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG03669 | hp1 | a0001 | c0001 | t0003 | g0008 | SAS | PJL | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG03669 | hp2 | a0001 | c0002 | t0001 | g0004 | SAS | PJL | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0071 | SAS | STU | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG03688 | hp2 | a0001 | c0001 | t0004 | g0015 | SAS | STU | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0082 | SAS | PJL | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG03831 | hp1 | a0001 | c0001 | t0003 | g0008 | SAS | BEB | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0148 | SAS | BEB | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG03834 | hp1 | a0001 | c0002 | t0001 | g0091 | SAS | BEB | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG03834 | hp2 | a0001 | c0002 | t0001 | g0035 | SAS | BEB | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG03927 | hp1 | a0001 | c0002 | t0001 | g0002 | SAS | BEB | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0028 | SAS | BEB | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG03942 | hp1 | a0001 | c0001 | t0021 | g0143 | SAS | BEB | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG03942 | hp2 | a0001 | c0001 | t0003 | g0008 | SAS | BEB | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0083 | SAS | STU | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | STU | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | BEB | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG04184 | hp2 | a0001 | c0002 | t0001 | g0025 | SAS | BEB | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG04199 | hp1 | a0001 | c0002 | t0001 | g0035 | SAS | STU | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG04199 | hp2 | a0001 | c0001 | t0004 | g0015 | SAS | STU | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG04204 | hp1 | a0001 | c0002 | t0001 | g0002 | SAS | STU | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG04204 | hp2 | a0001 | c0002 | t0001 | g0025 | SAS | STU | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG04228 | hp1 | a0001 | c0001 | t0003 | g0057 | SAS | STU | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG04228 | hp2 | a0001 | c0001 | t0004 | g0015 | SAS | STU | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | YRI | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | YRI | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA18612 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | CHB | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA18612 | hp2 | a0001 | c0002 | t0001 | g0006 | EAS | CHB | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA18747 | hp1 | a0001 | c0002 | t0001 | g0113 | EAS | CHB | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | CHB | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA18906 | hp1 | a0001 | c0001 | t0023 | g0139 | AFR | YRI | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | YRI | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA18939 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA18940 | hp1 | a0001 | c0002 | t0001 | g0116 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA18941 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA18942 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA18945 | hp2 | a0001 | c0001 | t0020 | g0134 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA18947 | hp2 | a0001 | c0002 | t0001 | g0109 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA18948 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA18951 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA18953 | hp2 | a0001 | c0002 | t0001 | g0119 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA18954 | hp1 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA18956 | hp1 | a0001 | c0002 | t0001 | g0118 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA18956 | hp2 | a0001 | c0001 | t0002 | g0144 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA18957 | hp1 | a0001 | c0002 | t0001 | g0096 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA18957 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0141 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA18962 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA18963 | hp2 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0152 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA18966 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0142 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA18968 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA18969 | hp1 | a0001 | c0001 | t0008 | g0145 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA18969 | hp2 | a0001 | c0002 | t0017 | g0108 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA18970 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA18972 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA18973 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA18974 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA18974 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA18975 | hp1 | a0001 | c0004 | t0001 | g0039 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA18975 | hp2 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA18977 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA18977 | hp2 | a0001 | c0002 | t0001 | g0105 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA18979 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA18980 | hp2 | a0001 | c0001 | t0019 | g0051 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA18984 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA18986 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA18987 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA18988 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA18988 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA18989 | hp1 | a0001 | c0001 | t0002 | g0150 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA18989 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA18991 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA18993 | hp1 | a0001 | c0002 | t0001 | g0026 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA18995 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA19000 | hp1 | a0001 | c0004 | t0001 | g0039 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA19000 | hp2 | a0001 | c0001 | t0022 | g0137 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA19001 | hp1 | a0001 | c0001 | t0007 | g0044 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA19001 | hp2 | a0001 | c0002 | t0001 | g0086 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA19004 | hp1 | a0001 | c0002 | t0001 | g0120 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA19004 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA19007 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA19009 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0146 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0149 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA19011 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | LWK | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA19030 | hp2 | a0001 | c0001 | t0005 | g0020 | AFR | LWK | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | LWK | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA19043 | hp2 | a0001 | c0003 | t0001 | g0054 | AFR | LWK | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA19054 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA19057 | hp1 | a0001 | c0002 | t0001 | g0122 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA19057 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA19058 | hp1 | a0001 | c0001 | t0007 | g0136 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA19059 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA19059 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA19060 | hp1 | a0001 | c0002 | t0001 | g0098 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA19063 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA19066 | hp1 | a0001 | c0001 | t0007 | g0044 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA19068 | hp1 | a0001 | c0002 | t0001 | g0100 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA19068 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA19070 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA19072 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA19072 | hp2 | a0001 | c0002 | t0001 | g0117 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA19074 | hp1 | a0001 | c0002 | t0001 | g0121 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA19078 | hp1 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA19078 | hp2 | a0001 | c0002 | t0001 | g0036 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA19079 | hp1 | a0001 | c0001 | t0015 | g0126 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA19079 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA19081 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA19081 | hp2 | a0001 | c0002 | t0001 | g0114 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA19082 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA19084 | hp1 | a0001 | c0002 | t0001 | g0036 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA19084 | hp2 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA19086 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA19086 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA19088 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA19088 | hp2 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA19090 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA19090 | hp2 | a0001 | c0002 | t0001 | g0026 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA19091 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | YRI | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | YRI | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA20129 | hp1 | a0001 | c0002 | t0001 | g0005 | AFR | ASW | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ASW | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA20752 | hp1 | a0001 | c0002 | t0001 | g0014 | EUR | TSI | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0001 | EUR | TSI | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA20805 | hp1 | a0001 | c0002 | t0001 | g0037 | EUR | TSI | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0001 | EUR | TSI | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA20905 | hp1 | a0001 | c0002 | t0001 | g0004 | SAS | GIH | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA20905 | hp2 | a0001 | c0001 | t0004 | g0015 | SAS | GIH | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG01123 | hp2 | a0001 | c0002 | t0001 | g0014 | AMR | CLM | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG02109 | hp2 | a0001 | c0001 | t0005 | g0020 | AFR | ACB | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | ACB | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG02559 | hp1 | a0001 | c0002 | t0001 | g0037 | AFR | ACB | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | MSL | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | USA | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| HG06807 | hp2 | a0001 | c0001 | t0003 | g0008 | AFR | USA | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA20300 | hp1 | a0001 | c0003 | t0001 | g0055 | AFR | USA | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | USA | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | LWK | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0043 | AFR | LWK | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0004 | g0015 | REF | REF | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| homoSapiens_grch38 | hp1 | a0001 | c0002 | t0001 | g0112 | REF | REF | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:95778896 | A | G | 4 | a0001c0001 a0001c0003 a0001c0004 others(1): Show |
250 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(247): Show |
synonymous_variant | LOW | c.754T>C | p.Leu252Leu | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 8/10 | 1058/3932 | 754/1020 | 252/339 | chr11 | 95778896 | |||
| chr11:95778921 | T | C | 1 | a0001c0003 | 3 | HG03041.hp1 NA19043.hp2 NA20300.hp1 |
synonymous_variant | LOW | c.729A>G | p.Thr243Thr | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 8/10 | 1033/3932 | 729/1020 | 243/339 | chr11 | 95778921 | |||
| chr11:95783249 | A | G | 1 | a0001c0004 | 2 | NA18975.hp1 NA19000.hp1 |
synonymous_variant | LOW | c.379T>C | p.Leu127Leu | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 5/10 | 683/3932 | 379/1020 | 127/339 | chr11 | 95783249 | |||
| chr11:95788507 | T | C | 1 | a0001c0005 | 2 | HG01346.hp1 HG02717.hp1 |
synonymous_variant | LOW | c.144A>G | p.Gln48Gln | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 2/10 | 448/3932 | 144/1020 | 48/339 | chr11 | 95788507 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:95768964 | G | A | 1 | a0001c0002t0006 | 3 | HG01069.hp2 HG01071.hp1 HG01074.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2597C>T | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 10/10 | 2597 | chr11 | 95768964 | ||||||
| chr11:95768964 | G | C | 6 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0010 others(3): Show |
96 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(93): Show |
3_prime_UTR_variant | MODIFIER | c.*2597C>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 10/10 | 2597 | chr11 | 95768964 | ||||||
| chr11:95769194 | G | A | 1 | a0001c0001t0010 | 2 | HG00639.hp2 HG01069.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2367C>T | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 10/10 | 2367 | chr11 | 95769194 | ||||||
| chr11:95769748 | A | G | 2 | a0001c0001t0004 a0001c0001t0019 |
8 | HG03239.hp2 HG03491.hp1 HG03688.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1813T>C | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 10/10 | 1813 | chr11 | 95769748 | ||||||
| chr11:95770005 | C | T | 1 | a0001c0001t0015 | 1 | NA19079.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1556G>A | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 10/10 | 1556 | chr11 | 95770005 | ||||||
| chr11:95770179 | T | G | 1 | a0001c0002t0009 | 2 | HG02015.hp1 HG02074.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1382A>C | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 10/10 | 1382 | chr11 | 95770179 | ||||||
| chr11:95770238 | C | T | 1 | a0001c0001t0022 | 1 | NA19000.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1323G>A | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 10/10 | 1323 | chr11 | 95770238 | ||||||
| chr11:95770472 | T | C | 9 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0008 others(6): Show |
101 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(98): Show |
3_prime_UTR_variant | MODIFIER | c.*1089A>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 10/10 | 1089 | chr11 | 95770472 | ||||||
| chr11:95770486 | A | C | 1 | a0001c0002t0012 | 1 | HG02258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1075T>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 10/10 | 1075 | chr11 | 95770486 | ||||||
| chr11:95770500 | T | A | 1 | a0001c0002t0017 | 1 | NA18969.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1061A>T | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 10/10 | 1061 | chr11 | 95770500 | ||||||
| chr11:95770614 | C | T | 1 | a0001c0001t0007 | 3 | NA19001.hp1 NA19058.hp1 NA19066.hp1 |
3_prime_UTR_variant | MODIFIER | c.*947G>A | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 10/10 | 947 | chr11 | 95770614 | ||||||
| chr11:95770993 | CTAA | C | 1 | a0001c0001t0003 | 15 | HG02300.hp1 HG02647.hp1 HG02735.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*565_*567delTTA | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 10/10 | 565 | chr11 | 95770993 | ||||||
| chr11:95771065 | T | G | 1 | a0001c0001t0018 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*496A>C | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 10/10 | 496 | chr11 | 95771065 | ||||||
| chr11:95771315 | A | G | 1 | a0001c0002t0014 | 1 | HG01358.hp2 | 3_prime_UTR_variant | MODIFIER | c.*246T>C | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 10/10 | 246 | chr11 | 95771315 | ||||||
| chr11:95771378 | A | C | 1 | a0001c0001t0021 | 1 | HG03942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*183T>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 10/10 | 183 | chr11 | 95771378 | ||||||
| chr11:95771436 | C | A | 1 | a0001c0001t0023 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*125G>T | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 10/10 | 125 | chr11 | 95771436 | ||||||
| chr11:95771483 | C | T | 1 | a0001c0001t0013 | 1 | HG01978.hp1 | 3_prime_UTR_variant | MODIFIER | c.*78G>A | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 10/10 | 78 | chr11 | 95771483 | ||||||
| chr11:95771523 | T | C | 1 | a0001c0001t0019 | 1 | NA18980.hp2 | 3_prime_UTR_variant | MODIFIER | c.*38A>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 10/10 | 38 | chr11 | 95771523 | ||||||
| chr11:95789485 | C | T | 1 | a0001c0001t0005 | 3 | HG02109.hp2 HG03540.hp1 NA19030.hp2 |
5_prime_UTR_variant | MODIFIER | c.-7G>A | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 1/10 | 7 | chr11 | 95789485 | ||||||
| chr11:95789602 | A | ACCAGGGC others(14): Show |
1 | a0001c0001t0020 | 1 | NA18945.hp2 | 5_prime_UTR_variant | MODIFIER | c.-145_-125dupGCTCTC others(15): Show |
FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 1/10 | 125 | chr11 | 95789602 | ||||||
| chr11:95789638 | A | G | 1 | a0001c0002t0012 | 1 | HG02258.hp2 | 5_prime_UTR_variant | MODIFIER | c.-160T>C | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 1/10 | 160 | chr11 | 95789638 | ||||||
| chr11:95789694 | G | C | 8 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0008 others(5): Show |
100 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(97): Show |
5_prime_UTR_variant | MODIFIER | c.-216C>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 1/10 | 216 | chr11 | 95789694 | ||||||
| chr11:95789743 | C | T | 1 | a0001c0001t0011 | 1 | HG03516.hp2 | 5_prime_UTR_variant | MODIFIER | c.-265G>A | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 1/10 | 265 | chr11 | 95789743 | ||||||
| chr11:95789758 | T | C | 1 | a0001c0001t0024 | 1 | HG02056.hp1 | 5_prime_UTR_variant | MODIFIER | c.-280A>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 1/10 | 280 | chr11 | 95789758 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:95771762 | G | C | 10 | a0001c0001t0001g0013 a0001c0001t0001g0022 a0001c0001t0001g0071 others(7): Show |
17 | HG00423.hp1 HG00558.hp1 HG01928.hp1 others(14): Show |
intron_variant | MODIFIER | c.931-112C>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 9/9 | chr11 | 95771762 | |||||||
| chr11:95771910 | A | T | 1 | a0001c0001t0019g0051 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.931-260T>A | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 9/9 | chr11 | 95771910 | |||||||
| chr11:95772063 | G | A | 44 | a0001c0001t0001g0010 a0001c0001t0001g0040 a0001c0001t0001g0041 others(41): Show |
124 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(121): Show |
intron_variant | MODIFIER | c.931-413C>T | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 9/9 | chr11 | 95772063 | |||||||
| chr11:95772093 | T | C | 14 | a0001c0001t0001g0010 a0001c0001t0001g0040 a0001c0001t0001g0041 others(11): Show |
24 | HG01081.hp1 HG01167.hp1 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.931-443A>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 9/9 | chr11 | 95772093 | |||||||
| chr11:95772110 | T | C | 3 | a0001c0001t0002g0012 a0001c0001t0002g0135 a0001c0001t0002g0142 |
9 | HG02080.hp1 NA18747.hp2 NA18968.hp1 others(6): Show |
intron_variant | MODIFIER | c.931-460A>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 9/9 | chr11 | 95772110 | |||||||
| chr11:95772486 | A | C | 1 | a0001c0001t0002g0142 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.931-836T>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 9/9 | chr11 | 95772486 | |||||||
| chr11:95772667 | T | C | 1 | a0001c0001t0002g0149 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.931-1017A>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 9/9 | chr11 | 95772667 | |||||||
| chr11:95772724 | G | A | 31 | a0001c0001t0001g0073 a0001c0001t0002g0001 a0001c0001t0002g0012 others(28): Show |
101 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(98): Show |
intron_variant | MODIFIER | c.931-1074C>T | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 9/9 | chr11 | 95772724 | |||||||
| chr11:95772931 | T | C | 1 | a0001c0001t0001g0019 | 4 | HG00738.hp2 HG00741.hp2 HG01099.hp1 others(1): Show |
intron_variant | MODIFIER | c.931-1281A>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 9/9 | chr11 | 95772931 | |||||||
| chr11:95773120 | GTTC | G | 30 | a0001c0001t0002g0001 a0001c0001t0002g0012 a0001c0001t0002g0027 others(27): Show |
100 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(97): Show |
intron_variant | MODIFIER | c.931-1473_931-1471d others(5): Show |
FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 9/9 | chr11 | 95773120 | |||||||
| chr11:95773429 | T | C | 1 | a0001c0001t0001g0067 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.931-1779A>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 9/9 | chr11 | 95773429 | |||||||
| chr11:95773458 | C | CA | 63 | a0001c0001t0001g0011 a0001c0001t0001g0017 a0001c0001t0001g0021 others(60): Show |
195 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.931-1809dupT | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 9/9 | chr11 | 95773458 | |||||||
| chr11:95773458 | C | CAA | 42 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0013 others(39): Show |
91 | HG00323.hp2 HG00558.hp1 HG00738.hp2 others(88): Show |
intron_variant | MODIFIER | c.931-1810_931-1809d others(4): Show |
FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 9/9 | chr11 | 95773458 | |||||||
| chr11:95773458 | C | CAAAAA | 28 | a0001c0001t0002g0001 a0001c0001t0002g0012 a0001c0001t0002g0027 others(25): Show |
97 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(94): Show |
intron_variant | MODIFIER | c.931-1813_931-1809d others(7): Show |
FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 9/9 | chr11 | 95773458 | |||||||
| chr11:95773505 | A | C | 1 | a0001c0001t0002g0141 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.931-1855T>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 9/9 | chr11 | 95773505 | |||||||
| chr11:95773624 | T | A | 1 | a0001c0002t0001g0107 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.931-1974A>T | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 9/9 | chr11 | 95773624 | |||||||
| chr11:95773743 | G | C | 31 | a0001c0001t0002g0001 a0001c0001t0002g0012 a0001c0001t0002g0027 others(28): Show |
101 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(98): Show |
intron_variant | MODIFIER | c.931-2093C>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 9/9 | chr11 | 95773743 | |||||||
| chr11:95773864 | T | C | 8 | a0001c0001t0001g0031 a0001c0001t0003g0008 a0001c0001t0003g0030 others(5): Show |
17 | HG02300.hp1 HG02630.hp1 HG02647.hp1 others(14): Show |
intron_variant | MODIFIER | c.930+2058A>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 9/9 | chr11 | 95773864 | |||||||
| chr11:95773894 | T | C | 1 | a0001c0002t0001g0106 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.930+2028A>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 9/9 | chr11 | 95773894 | |||||||
| chr11:95774053 | G | C | 8 | a0001c0001t0001g0011 a0001c0001t0001g0017 a0001c0001t0001g0062 others(5): Show |
19 | HG01123.hp1 HG02055.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.930+1869C>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 9/9 | chr11 | 95774053 | |||||||
| chr11:95774095 | A | T | 1 | a0001c0001t0002g0154 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.930+1827T>A | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 9/9 | chr11 | 95774095 | |||||||
| chr11:95774205 | CAG | C | 1 | a0001c0002t0001g0025 | 3 | HG02683.hp2 HG04184.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.930+1715_930+1716d others(4): Show |
FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 9/9 | chr11 | 95774205 | |||||||
| chr11:95774243 | T | A | 3 | a0001c0001t0004g0015 a0001c0001t0004g0029 a0001c0001t0019g0051 |
8 | HG03239.hp2 HG03491.hp1 HG03688.hp2 others(5): Show |
intron_variant | MODIFIER | c.930+1679A>T | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 9/9 | chr11 | 95774243 | |||||||
| chr11:95774460 | C | A | 144 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0010 others(141): Show |
376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.930+1462G>T | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 9/9 | chr11 | 95774460 | |||||||
| chr11:95774491 | C | A | 1 | a0001c0001t0001g0129 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.930+1431G>T | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 9/9 | chr11 | 95774491 | |||||||
| chr11:95774530 | T | C | 1 | a0001c0002t0001g0121 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.930+1392A>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 9/9 | chr11 | 95774530 | |||||||
| chr11:95774708 | TATAAGA | T | 30 | a0001c0001t0002g0001 a0001c0001t0002g0012 a0001c0001t0002g0027 others(27): Show |
100 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(97): Show |
intron_variant | MODIFIER | c.930+1208_930+1213d others(8): Show |
FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 9/9 | chr11 | 95774708 | |||||||
| chr11:95774709 | A | G | 1 | a0001c0002t0001g0116 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.930+1213T>C | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 9/9 | chr11 | 95774709 | |||||||
| chr11:95774791 | A | G | 1 | a0001c0001t0002g0027 | 3 | HG00140.hp1 HG00741.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.930+1131T>C | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 9/9 | chr11 | 95774791 | |||||||
| chr11:95774856 | T | C | 54 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0011 others(51): Show |
116 | HG00323.hp2 HG00423.hp1 HG00558.hp1 others(113): Show |
intron_variant | MODIFIER | c.930+1066A>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 9/9 | chr11 | 95774856 | |||||||
| chr11:95774875 | A | T | 1 | a0001c0001t0001g0125 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.930+1047T>A | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 9/9 | chr11 | 95774875 | |||||||
| chr11:95774957 | A | G | 99 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0010 others(96): Show |
241 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(238): Show |
intron_variant | MODIFIER | c.930+965T>C | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 9/9 | chr11 | 95774957 | |||||||
| chr11:95775003 | G | GA | 21 | a0001c0001t0001g0053 a0001c0001t0001g0061 a0001c0001t0016g0049 others(18): Show |
53 | HG00597.hp1 HG00673.hp1 HG01081.hp2 others(50): Show |
intron_variant | MODIFIER | c.930+918dupT | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 9/9 | chr11 | 95775003 | |||||||
| chr11:95775003 | GA | G | 20 | a0001c0001t0001g0010 a0001c0001t0001g0040 a0001c0001t0001g0041 others(17): Show |
37 | HG01081.hp1 HG01167.hp1 HG01169.hp2 others(34): Show |
intron_variant | MODIFIER | c.930+918delT | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 9/9 | chr11 | 95775003 | |||||||
| chr11:95775005 | A | G | 14 | a0001c0001t0001g0010 a0001c0001t0001g0040 a0001c0001t0001g0041 others(11): Show |
24 | HG01081.hp1 HG01167.hp1 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.930+917T>C | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 9/9 | chr11 | 95775005 | |||||||
| chr11:95775013 | A | C | 1 | a0001c0002t0001g0036 | 2 | NA19078.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.930+909T>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 9/9 | chr11 | 95775013 | |||||||
| chr11:95775036 | T | G | 14 | a0001c0001t0001g0010 a0001c0001t0001g0040 a0001c0001t0001g0041 others(11): Show |
24 | HG01081.hp1 HG01167.hp1 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.930+886A>C | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 9/9 | chr11 | 95775036 | |||||||
| chr11:95775188 | T | C | 1 | a0001c0001t0001g0074 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.930+734A>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 9/9 | chr11 | 95775188 | |||||||
| chr11:95775219 | G | T | 45 | a0001c0001t0001g0010 a0001c0001t0001g0040 a0001c0001t0001g0041 others(42): Show |
125 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(122): Show |
intron_variant | MODIFIER | c.930+703C>A | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 9/9 | chr11 | 95775219 | |||||||
| chr11:95775220 | T | C | 9 | a0001c0001t0001g0007 a0001c0001t0001g0018 a0001c0001t0001g0023 others(6): Show |
27 | HG01074.hp1 HG01109.hp2 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.930+702A>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 9/9 | chr11 | 95775220 | |||||||
| chr11:95775233 | A | T | 14 | a0001c0001t0001g0010 a0001c0001t0001g0040 a0001c0001t0001g0041 others(11): Show |
24 | HG01081.hp1 HG01167.hp1 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.930+689T>A | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 9/9 | chr11 | 95775233 | |||||||
| chr11:95775240 | C | A | 45 | a0001c0001t0001g0010 a0001c0001t0001g0040 a0001c0001t0001g0041 others(42): Show |
125 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(122): Show |
intron_variant | MODIFIER | c.930+682G>T | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 9/9 | chr11 | 95775240 | |||||||
| chr11:95775262 | G | C | 1 | a0001c0001t0001g0075 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.930+660C>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 9/9 | chr11 | 95775262 | |||||||
| chr11:95775360 | C | A | 45 | a0001c0001t0001g0010 a0001c0001t0001g0040 a0001c0001t0001g0041 others(42): Show |
125 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(122): Show |
intron_variant | MODIFIER | c.930+562G>T | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 9/9 | chr11 | 95775360 | |||||||
| chr11:95775398 | T | C | 14 | a0001c0001t0001g0010 a0001c0001t0001g0040 a0001c0001t0001g0041 others(11): Show |
24 | HG01081.hp1 HG01167.hp1 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.930+524A>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 9/9 | chr11 | 95775398 | |||||||
| chr11:95775571 | T | C | 3 | a0001c0001t0004g0015 a0001c0001t0004g0029 a0001c0001t0019g0051 |
8 | HG03239.hp2 HG03491.hp1 HG03688.hp2 others(5): Show |
intron_variant | MODIFIER | c.930+351A>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 9/9 | chr11 | 95775571 | |||||||
| chr11:95775599 | A | G | 1 | a0001c0002t0001g0035 | 2 | HG03834.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.930+323T>C | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 9/9 | chr11 | 95775599 | |||||||
| chr11:95775638 | CA | C | 14 | a0001c0001t0001g0010 a0001c0001t0001g0040 a0001c0001t0001g0041 others(11): Show |
24 | HG01081.hp1 HG01167.hp1 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.930+283delT | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 9/9 | chr11 | 95775638 | |||||||
| chr11:95775757 | C | T | 1 | a0001c0003t0001g0054 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.930+165G>A | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 9/9 | chr11 | 95775757 | |||||||
| chr11:95775873 | C | G | 29 | a0001c0001t0002g0001 a0001c0001t0002g0012 a0001c0001t0002g0027 others(26): Show |
99 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(96): Show |
intron_variant | MODIFIER | c.930+49G>C | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 9/9 | chr11 | 95775873 | |||||||
| chr11:95776178 | G | C | 1 | a0001c0002t0001g0109 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.829-155C>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 8/9 | chr11 | 95776178 | |||||||
| chr11:95776240 | C | T | 14 | a0001c0001t0001g0010 a0001c0001t0001g0040 a0001c0001t0001g0041 others(11): Show |
24 | HG01081.hp1 HG01167.hp1 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.829-217G>A | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 8/9 | chr11 | 95776240 | |||||||
| chr11:95776474 | T | C | 28 | a0001c0001t0002g0001 a0001c0001t0002g0012 a0001c0001t0002g0027 others(25): Show |
97 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(94): Show |
intron_variant | MODIFIER | c.829-451A>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 8/9 | chr11 | 95776474 | |||||||
| chr11:95776475 | G | C | 1 | a0001c0001t0001g0128 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.829-452C>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 8/9 | chr11 | 95776475 | |||||||
| chr11:95776533 | T | C | 1 | a0001c0002t0001g0110 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.829-510A>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 8/9 | chr11 | 95776533 | |||||||
| chr11:95776554 | T | A | 1 | a0001c0001t0001g0068 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.829-531A>T | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 8/9 | chr11 | 95776554 | |||||||
| chr11:95776913 | G | A | 1 | a0001c0001t0002g0144 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.829-890C>T | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 8/9 | chr11 | 95776913 | |||||||
| chr11:95776925 | C | T | 30 | a0001c0001t0002g0001 a0001c0001t0002g0012 a0001c0001t0002g0027 others(27): Show |
100 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(97): Show |
intron_variant | MODIFIER | c.829-902G>A | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 8/9 | chr11 | 95776925 | |||||||
| chr11:95776930 | TA | T | 6 | a0001c0001t0001g0017 a0001c0001t0001g0062 a0001c0001t0001g0063 others(3): Show |
9 | HG02055.hp1 HG02257.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.829-908delT | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 8/9 | chr11 | 95776930 | |||||||
| chr11:95777067 | C | T | 1 | a0001c0001t0016g0049 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.829-1044G>A | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 8/9 | chr11 | 95777067 | |||||||
| chr11:95777273 | T | A | 1 | a0001c0001t0002g0146 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.829-1250A>T | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 8/9 | chr11 | 95777273 | |||||||
| chr11:95777344 | A | G | 33 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0013 others(30): Show |
75 | HG00323.hp2 HG00423.hp1 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.829-1321T>C | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 8/9 | chr11 | 95777344 | |||||||
| chr11:95777463 | C | A | 1 | a0001c0002t0001g0117 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.828+1359G>T | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 8/9 | chr11 | 95777463 | |||||||
| chr11:95777697 | T | C | 1 | a0001c0001t0002g0147 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.828+1125A>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 8/9 | chr11 | 95777697 | |||||||
| chr11:95777814 | A | G | 1 | a0001c0001t0001g0071 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.828+1008T>C | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 8/9 | chr11 | 95777814 | |||||||
| chr11:95777856 | T | C | 1 | a0001c0001t0002g0148 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.828+966A>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 8/9 | chr11 | 95777856 | |||||||
| chr11:95777858 | T | C | 1 | a0001c0002t0001g0115 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.828+964A>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 8/9 | chr11 | 95777858 | |||||||
| chr11:95777999 | C | T | 1 | a0001c0002t0001g0105 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.828+823G>A | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 8/9 | chr11 | 95777999 | |||||||
| chr11:95778234 | C | A | 1 | a0001c0005t0001g0038 | 2 | HG01346.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.828+588G>T | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 8/9 | chr11 | 95778234 | |||||||
| chr11:95778281 | C | A | 30 | a0001c0001t0002g0001 a0001c0001t0002g0012 a0001c0001t0002g0027 others(27): Show |
100 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(97): Show |
intron_variant | MODIFIER | c.828+541G>T | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 8/9 | chr11 | 95778281 | |||||||
| chr11:95778343 | G | C | 1 | a0001c0001t0016g0049 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.828+479C>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 8/9 | chr11 | 95778343 | |||||||
| chr11:95778405 | G | A | 1 | a0001c0002t0001g0111 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.828+417C>T | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 8/9 | chr11 | 95778405 | |||||||
| chr11:95778484 | A | C | 1 | a0001c0001t0002g0140 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.828+338T>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 8/9 | chr11 | 95778484 | |||||||
| chr11:95778761 | C | T | 1 | a0001c0001t0001g0019 | 4 | HG00738.hp2 HG00741.hp2 HG01099.hp1 others(1): Show |
intron_variant | MODIFIER | c.828+61G>A | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 8/9 | chr11 | 95778761 | |||||||
| chr11:95779581 | A | G | 1 | a0001c0002t0001g0104 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.692+26T>C | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 7/9 | chr11 | 95779581 | |||||||
| chr11:95779593 | G | A | 1 | a0001c0001t0001g0079 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.692+14C>T | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 7/9 | chr11 | 95779593 | |||||||
| chr11:95779976 | C | T | 1 | a0001c0001t0018g0050 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.564-50G>A | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 5/9 | chr11 | 95779976 | |||||||
| chr11:95779993 | C | A | 1 | a0001c0001t0001g0076 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.564-67G>T | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 5/9 | chr11 | 95779993 | |||||||
| chr11:95780023 | T | C | 1 | a0001c0002t0001g0103 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.564-97A>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 5/9 | chr11 | 95780023 | |||||||
| chr11:95780044 | G | A | 3 | a0001c0001t0001g0032 a0001c0001t0001g0065 a0001c0001t0001g0077 |
4 | HG02818.hp2 HG02922.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.564-118C>T | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 5/9 | chr11 | 95780044 | |||||||
| chr11:95780194 | A | C | 1 | a0001c0002t0001g0102 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.564-268T>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 5/9 | chr11 | 95780194 | |||||||
| chr11:95780197 | G | A | 1 | a0001c0002t0001g0102 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.564-271C>T | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 5/9 | chr11 | 95780197 | |||||||
| chr11:95780198 | T | A | 1 | a0001c0002t0001g0102 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.564-272A>T | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 5/9 | chr11 | 95780198 | |||||||
| chr11:95780200 | G | C | 1 | a0001c0001t0001g0033 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.564-274C>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 5/9 | chr11 | 95780200 | |||||||
| chr11:95780208 | A | G | 1 | a0001c0002t0001g0102 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.564-282T>C | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 5/9 | chr11 | 95780208 | |||||||
| chr11:95780209 | A | G | 1 | a0001c0002t0001g0102 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.564-283T>C | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 5/9 | chr11 | 95780209 | |||||||
| chr11:95780211 | T | G | 1 | a0001c0002t0001g0102 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.564-285A>C | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 5/9 | chr11 | 95780211 | |||||||
| chr11:95780214 | T | G | 1 | a0001c0002t0001g0102 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.564-288A>C | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 5/9 | chr11 | 95780214 | |||||||
| chr11:95780220 | T | G | 1 | a0001c0002t0001g0102 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.564-294A>C | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 5/9 | chr11 | 95780220 | |||||||
| chr11:95780221 | G | C | 1 | a0001c0002t0001g0102 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.564-295C>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 5/9 | chr11 | 95780221 | |||||||
| chr11:95780227 | G | C | 1 | a0001c0002t0001g0102 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.564-301C>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 5/9 | chr11 | 95780227 | |||||||
| chr11:95780228 | T | C | 1 | a0001c0002t0001g0102 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.564-302A>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 5/9 | chr11 | 95780228 | |||||||
| chr11:95780230 | T | C | 1 | a0001c0002t0001g0102 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.564-304A>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 5/9 | chr11 | 95780230 | |||||||
| chr11:95780231 | A | C | 1 | a0001c0002t0001g0102 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.564-305T>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 5/9 | chr11 | 95780231 | |||||||
| chr11:95780232 | G | C | 1 | a0001c0002t0001g0102 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.564-306C>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 5/9 | chr11 | 95780232 | |||||||
| chr11:95780233 | G | A | 1 | a0001c0002t0001g0102 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.564-307C>T | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 5/9 | chr11 | 95780233 | |||||||
| chr11:95780234 | T | C | 1 | a0001c0002t0001g0102 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.564-308A>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 5/9 | chr11 | 95780234 | |||||||
| chr11:95780240 | T | A | 1 | a0001c0002t0001g0102 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.564-314A>T | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 5/9 | chr11 | 95780240 | |||||||
| chr11:95780245 | T | C | 1 | a0001c0002t0001g0102 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.564-319A>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 5/9 | chr11 | 95780245 | |||||||
| chr11:95780246 | T | C | 1 | a0001c0002t0001g0102 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.564-320A>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 5/9 | chr11 | 95780246 | |||||||
| chr11:95780247 | T | C | 1 | a0001c0002t0001g0102 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.564-321A>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 5/9 | chr11 | 95780247 | |||||||
| chr11:95780248 | G | C | 1 | a0001c0002t0001g0102 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.564-322C>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 5/9 | chr11 | 95780248 | |||||||
| chr11:95780249 | G | C | 1 | a0001c0002t0001g0102 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.564-323C>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 5/9 | chr11 | 95780249 | |||||||
| chr11:95780333 | G | C | 54 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0011 others(51): Show |
116 | HG00323.hp2 HG00423.hp1 HG00558.hp1 others(113): Show |
intron_variant | MODIFIER | c.564-407C>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 5/9 | chr11 | 95780333 | |||||||
| chr11:95780353 | A | G | 2 | a0001c0001t0001g0022 a0001c0001t0013g0070 |
4 | HG01928.hp1 HG01975.hp2 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.564-427T>C | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 5/9 | chr11 | 95780353 | |||||||
| chr11:95780428 | A | G | 1 | a0001c0002t0001g0116 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.564-502T>C | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 5/9 | chr11 | 95780428 | |||||||
| chr11:95780487 | A | C | 1 | a0001c0002t0001g0103 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.564-561T>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 5/9 | chr11 | 95780487 | |||||||
| chr11:95780621 | A | G | 1 | a0001c0002t0001g0095 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.564-695T>C | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 5/9 | chr11 | 95780621 | |||||||
| chr11:95780651 | T | A | 1 | a0001c0001t0007g0136 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.564-725A>T | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 5/9 | chr11 | 95780651 | |||||||
| chr11:95780740 | C | T | 3 | a0001c0003t0001g0054 a0001c0003t0001g0055 a0001c0003t0001g0056 |
3 | HG03041.hp1 NA19043.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.564-814G>A | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 5/9 | chr11 | 95780740 | |||||||
| chr11:95780789 | T | C | 1 | a0001c0001t0002g0149 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.564-863A>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 5/9 | chr11 | 95780789 | |||||||
| chr11:95780852 | C | T | 1 | a0001c0003t0001g0054 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.564-926G>A | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 5/9 | chr11 | 95780852 | |||||||
| chr11:95780862 | C | T | 1 | a0001c0002t0001g0102 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.564-936G>A | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 5/9 | chr11 | 95780862 | |||||||
| chr11:95780902 | A | G | 1 | a0001c0001t0024g0155 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.564-976T>C | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 5/9 | chr11 | 95780902 | |||||||
| chr11:95780927 | G | T | 2 | a0001c0001t0003g0030 a0001c0001t0003g0058 |
3 | HG02818.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.564-1001C>A | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 5/9 | chr11 | 95780927 | |||||||
| chr11:95781000 | T | A | 1 | a0001c0001t0002g0151 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.564-1074A>T | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 5/9 | chr11 | 95781000 | |||||||
| chr11:95781011 | A | G | 1 | a0001c0001t0001g0066 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.564-1085T>C | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 5/9 | chr11 | 95781011 | |||||||
| chr11:95781077 | TC | T | 3 | a0001c0001t0001g0062 a0001c0001t0001g0069 a0001c0001t0002g0153 |
3 | HG01516.hp1 HG02055.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.564-1152delG | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 5/9 | chr11 | 95781077 | |||||||
| chr11:95781080 | C | T | 151 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0010 others(148): Show |
412 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(409): Show |
intron_variant | MODIFIER | c.564-1154G>A | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 5/9 | chr11 | 95781080 | |||||||
| chr11:95781092 | T | C | 25 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0016 others(22): Show |
54 | HG00323.hp2 HG00423.hp1 HG00558.hp1 others(51): Show |
intron_variant | MODIFIER | c.564-1166A>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 5/9 | chr11 | 95781092 | |||||||
| chr11:95781357 | C | T | 5 | a0001c0001t0001g0125 a0001c0001t0001g0127 a0001c0001t0001g0132 others(2): Show |
6 | NA18940.hp2 NA18945.hp1 NA18975.hp1 others(3): Show |
intron_variant | MODIFIER | c.564-1431G>A | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 5/9 | chr11 | 95781357 | |||||||
| chr11:95781435 | T | A | 31 | a0001c0001t0002g0001 a0001c0001t0002g0012 a0001c0001t0002g0027 others(28): Show |
101 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(98): Show |
intron_variant | MODIFIER | c.564-1509A>T | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 5/9 | chr11 | 95781435 | |||||||
| chr11:95781622 | G | A | 1 | a0001c0002t0001g0114 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.563+1443C>T | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 5/9 | chr11 | 95781622 | |||||||
| chr11:95781656 | G | A | 1 | a0001c0002t0012g0048 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.563+1409C>T | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 5/9 | chr11 | 95781656 | |||||||
| chr11:95781825 | CACT | C | 9 | a0001c0001t0001g0010 a0001c0001t0001g0041 a0001c0001t0001g0125 others(6): Show |
18 | HG01167.hp1 HG01169.hp2 HG02056.hp1 others(15): Show |
intron_variant | MODIFIER | c.563+1237_563+1239d others(5): Show |
FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 5/9 | chr11 | 95781825 | |||||||
| chr11:95781870 | T | G | 1 | a0001c0002t0001g0115 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.563+1195A>C | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 5/9 | chr11 | 95781870 | |||||||
| chr11:95781969 | G | A | 1 | a0001c0003t0001g0056 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.563+1096C>T | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 5/9 | chr11 | 95781969 | |||||||
| chr11:95782280 | A | G | 1 | a0001c0002t0001g0101 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.563+785T>C | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 5/9 | chr11 | 95782280 | |||||||
| chr11:95782328 | C | A | 3 | a0001c0002t0001g0026 a0001c0002t0001g0116 a0001c0002t0001g0117 |
5 | HG02129.hp1 NA18940.hp1 NA18993.hp1 others(2): Show |
intron_variant | MODIFIER | c.563+737G>T | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 5/9 | chr11 | 95782328 | |||||||
| chr11:95782328 | C | T | 37 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0013 others(34): Show |
79 | HG00323.hp2 HG00423.hp1 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.563+737G>A | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 5/9 | chr11 | 95782328 | |||||||
| chr11:95782375 | T | G | 1 | a0001c0001t0002g0150 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.563+690A>C | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 5/9 | chr11 | 95782375 | |||||||
| chr11:95782556 | G | A | 14 | a0001c0001t0001g0010 a0001c0001t0001g0040 a0001c0001t0001g0041 others(11): Show |
24 | HG01081.hp1 HG01167.hp1 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.563+509C>T | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 5/9 | chr11 | 95782556 | |||||||
| chr11:95782729 | A | C | 1 | a0001c0001t0003g0057 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.563+336T>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 5/9 | chr11 | 95782729 | |||||||
| chr11:95782745 | T | C | 1 | a0001c0001t0003g0060 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.563+320A>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 5/9 | chr11 | 95782745 | |||||||
| chr11:95782876 | C | A | 45 | a0001c0001t0001g0010 a0001c0001t0001g0040 a0001c0001t0001g0041 others(42): Show |
125 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(122): Show |
intron_variant | MODIFIER | c.563+189G>T | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 5/9 | chr11 | 95782876 | |||||||
| chr11:95783372 | A | G | 108 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0010 others(105): Show |
260 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(257): Show |
intron_variant | MODIFIER | c.364-108T>C | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 4/9 | chr11 | 95783372 | |||||||
| chr11:95783394 | T | G | 8 | a0001c0001t0001g0011 a0001c0001t0001g0017 a0001c0001t0001g0062 others(5): Show |
19 | HG01123.hp1 HG02055.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.364-130A>C | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 4/9 | chr11 | 95783394 | |||||||
| chr11:95783415 | G | A | 1 | a0001c0001t0001g0131 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.364-151C>T | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 4/9 | chr11 | 95783415 | |||||||
| chr11:95783459 | G | C | 1 | a0001c0001t0001g0023 | 3 | HG01891.hp2 HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.364-195C>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 4/9 | chr11 | 95783459 | |||||||
| chr11:95783553 | A | G | 8 | a0001c0001t0001g0031 a0001c0001t0003g0008 a0001c0001t0003g0030 others(5): Show |
17 | HG02300.hp1 HG02630.hp1 HG02647.hp1 others(14): Show |
intron_variant | MODIFIER | c.364-289T>C | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 4/9 | chr11 | 95783553 | |||||||
| chr11:95783567 | A | C | 24 | a0001c0001t0002g0001 a0001c0001t0002g0012 a0001c0001t0002g0042 others(21): Show |
88 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.364-303T>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 4/9 | chr11 | 95783567 | |||||||
| chr11:95783671 | C | T | 1 | a0001c0001t0001g0065 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.364-407G>A | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 4/9 | chr11 | 95783671 | |||||||
| chr11:95783721 | C | T | 3 | a0001c0001t0004g0015 a0001c0001t0004g0029 a0001c0001t0019g0051 |
8 | HG03239.hp2 HG03491.hp1 HG03688.hp2 others(5): Show |
intron_variant | MODIFIER | c.364-457G>A | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 4/9 | chr11 | 95783721 | |||||||
| chr11:95783982 | T | C | 1 | a0001c0001t0016g0049 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.364-718A>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 4/9 | chr11 | 95783982 | |||||||
| chr11:95784009 | G | A | 4 | a0001c0001t0001g0040 a0001c0001t0001g0129 a0001c0001t0001g0130 others(1): Show |
5 | HG01081.hp1 HG02280.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.364-745C>T | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 4/9 | chr11 | 95784009 | |||||||
| chr11:95784074 | T | C | 1 | a0001c0001t0001g0053 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.364-810A>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 4/9 | chr11 | 95784074 | |||||||
| chr11:95784265 | C | A | 1 | a0001c0001t0001g0063 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.364-1001G>T | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 4/9 | chr11 | 95784265 | |||||||
| chr11:95784382 | T | C | 1 | a0001c0002t0001g0118 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.364-1118A>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 4/9 | chr11 | 95784382 | |||||||
| chr11:95784412 | C | T | 32 | a0001c0001t0001g0130 a0001c0001t0002g0001 a0001c0001t0002g0012 others(29): Show |
102 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(99): Show |
intron_variant | MODIFIER | c.364-1148G>A | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 4/9 | chr11 | 95784412 | |||||||
| chr11:95784493 | A | G | 1 | a0001c0001t0023g0139 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.364-1229T>C | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 4/9 | chr11 | 95784493 | |||||||
| chr11:95784522 | G | T | 1 | a0001c0001t0002g0042 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.364-1258C>A | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 4/9 | chr11 | 95784522 | |||||||
| chr11:95784531 | G | T | 1 | a0001c0001t0001g0053 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.364-1267C>A | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 4/9 | chr11 | 95784531 | |||||||
| chr11:95784553 | A | AGT | 1 | a0001c0001t0001g0019 | 4 | HG00738.hp2 HG00741.hp2 HG01099.hp1 others(1): Show |
intron_variant | MODIFIER | c.364-1291_364-1290d others(4): Show |
FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 4/9 | chr11 | 95784553 | |||||||
| chr11:95784571 | T | TAC | 19 | a0001c0001t0001g0011 a0001c0001t0001g0017 a0001c0001t0001g0062 others(16): Show |
39 | HG00642.hp2 HG00735.hp2 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.364-1309_364-1308d others(4): Show |
FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 4/9 | chr11 | 95784571 | |||||||
| chr11:95784573 | C | T | 45 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0040 others(42): Show |
128 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(125): Show |
intron_variant | MODIFIER | c.364-1309G>A | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 4/9 | chr11 | 95784573 | |||||||
| chr11:95784593 | A | T | 1 | a0001c0002t0001g0089 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.364-1329T>A | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 4/9 | chr11 | 95784593 | |||||||
| chr11:95784622 | C | G | 1 | a0001c0002t0001g0100 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.364-1358G>C | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 4/9 | chr11 | 95784622 | |||||||
| chr11:95784681 | G | C | 1 | a0001c0001t0001g0080 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.364-1417C>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 4/9 | chr11 | 95784681 | |||||||
| chr11:95784818 | A | T | 37 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0013 others(34): Show |
79 | HG00323.hp2 HG00423.hp1 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.363+1301T>A | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 4/9 | chr11 | 95784818 | |||||||
| chr11:95784942 | G | C | 1 | a0001c0001t0001g0041 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.363+1177C>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 4/9 | chr11 | 95784942 | |||||||
| chr11:95785341 | T | C | 14 | a0001c0001t0001g0010 a0001c0001t0001g0040 a0001c0001t0001g0041 others(11): Show |
24 | HG01081.hp1 HG01167.hp1 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.363+778A>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 4/9 | chr11 | 95785341 | |||||||
| chr11:95785368 | A | G | 1 | a0001c0001t0002g0138 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.363+751T>C | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 4/9 | chr11 | 95785368 | |||||||
| chr11:95785443 | C | G | 3 | a0001c0001t0004g0015 a0001c0001t0004g0029 a0001c0001t0019g0051 |
8 | HG03239.hp2 HG03491.hp1 HG03688.hp2 others(5): Show |
intron_variant | MODIFIER | c.363+676G>C | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 4/9 | chr11 | 95785443 | |||||||
| chr11:95785452 | A | G | 1 | a0001c0002t0009g0034 | 2 | HG02015.hp1 HG02074.hp2 |
intron_variant | MODIFIER | c.363+667T>C | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 4/9 | chr11 | 95785452 | |||||||
| chr11:95785526 | T | C | 1 | a0001c0001t0011g0047 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.363+593A>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 4/9 | chr11 | 95785526 | |||||||
| chr11:95785698 | A | C | 1 | a0001c0001t0003g0052 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.363+421T>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 4/9 | chr11 | 95785698 | |||||||
| chr11:95785907 | G | A | 1 | a0001c0002t0001g0121 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.363+212C>T | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 4/9 | chr11 | 95785907 | |||||||
| chr11:95785914 | T | C | 1 | a0001c0002t0001g0098 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.363+205A>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 4/9 | chr11 | 95785914 | |||||||
| chr11:95785951 | A | C | 1 | a0001c0001t0022g0137 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.363+168T>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 4/9 | chr11 | 95785951 | |||||||
| chr11:95785993 | T | C | 14 | a0001c0001t0001g0010 a0001c0001t0001g0040 a0001c0001t0001g0041 others(11): Show |
24 | HG01081.hp1 HG01167.hp1 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.363+126A>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 4/9 | chr11 | 95785993 | |||||||
| chr11:95786031 | A | T | 45 | a0001c0001t0001g0010 a0001c0001t0001g0040 a0001c0001t0001g0041 others(42): Show |
125 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(122): Show |
intron_variant | MODIFIER | c.363+88T>A | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 4/9 | chr11 | 95786031 | |||||||
| chr11:95786079 | T | C | 54 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0011 others(51): Show |
116 | HG00323.hp2 HG00423.hp1 HG00558.hp1 others(113): Show |
intron_variant | MODIFIER | c.363+40A>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 4/9 | chr11 | 95786079 | |||||||
| chr11:95786093 | G | A | 2 | a0001c0002t0001g0087 a0001c0002t0001g0098 |
2 | HG02155.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.363+26C>T | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 4/9 | chr11 | 95786093 | |||||||
| chr11:95786323 | G | A | 2 | a0001c0001t0001g0040 a0001c0001t0001g0130 |
3 | HG02280.hp1 HG02630.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.208-49C>T | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 3/9 | chr11 | 95786323 | |||||||
| chr11:95786342 | G | A | 45 | a0001c0001t0001g0010 a0001c0001t0001g0040 a0001c0001t0001g0041 others(42): Show |
125 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(122): Show |
intron_variant | MODIFIER | c.208-68C>T | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 3/9 | chr11 | 95786342 | |||||||
| chr11:95786368 | A | G | 1 | a0001c0002t0001g0088 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.208-94T>C | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 3/9 | chr11 | 95786368 | |||||||
| chr11:95786475 | G | T | 1 | a0001c0002t0001g0099 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.208-201C>A | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 3/9 | chr11 | 95786475 | |||||||
| chr11:95786494 | C | T | 14 | a0001c0001t0001g0010 a0001c0001t0001g0040 a0001c0001t0001g0041 others(11): Show |
24 | HG01081.hp1 HG01167.hp1 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.208-220G>A | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 3/9 | chr11 | 95786494 | |||||||
| chr11:95786623 | C | T | 45 | a0001c0001t0001g0010 a0001c0001t0001g0040 a0001c0001t0001g0041 others(42): Show |
125 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(122): Show |
intron_variant | MODIFIER | c.208-349G>A | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 3/9 | chr11 | 95786623 | |||||||
| chr11:95786714 | A | G | 1 | a0001c0001t0002g0042 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.208-440T>C | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 3/9 | chr11 | 95786714 | |||||||
| chr11:95786775 | A | G | 6 | a0001c0002t0001g0006 a0001c0002t0001g0087 a0001c0002t0001g0095 others(3): Show |
18 | HG00597.hp1 HG01081.hp2 HG01256.hp1 others(15): Show |
intron_variant | MODIFIER | c.208-501T>C | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 3/9 | chr11 | 95786775 | |||||||
| chr11:95786874 | T | C | 1 | a0001c0001t0001g0131 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.208-600A>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 3/9 | chr11 | 95786874 | |||||||
| chr11:95786910 | T | G | 1 | a0001c0001t0001g0081 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.208-636A>C | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 3/9 | chr11 | 95786910 | |||||||
| chr11:95787110 | G | C | 1 | a0001c0001t0016g0049 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.207+514C>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 3/9 | chr11 | 95787110 | |||||||
| chr11:95787140 | T | G | 2 | a0001c0001t0001g0082 a0001c0001t0001g0083 |
2 | HG03704.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.207+484A>C | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 3/9 | chr11 | 95787140 | |||||||
| chr11:95787144 | C | A | 1 | a0001c0001t0001g0064 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.207+480G>T | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 3/9 | chr11 | 95787144 | |||||||
| chr11:95787242 | T | G | 14 | a0001c0001t0001g0010 a0001c0001t0001g0040 a0001c0001t0001g0041 others(11): Show |
24 | HG01081.hp1 HG01167.hp1 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.207+382A>C | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 3/9 | chr11 | 95787242 | |||||||
| chr11:95787319 | C | T | 11 | a0001c0002t0001g0005 a0001c0002t0001g0014 a0001c0002t0001g0088 others(8): Show |
32 | HG00642.hp2 HG00735.hp2 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.207+305G>A | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 3/9 | chr11 | 95787319 | |||||||
| chr11:95787356 | C | T | 1 | a0001c0001t0007g0136 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.207+268G>A | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 3/9 | chr11 | 95787356 | |||||||
| chr11:95787408 | T | G | 1 | a0001c0002t0001g0122 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.207+216A>C | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 3/9 | chr11 | 95787408 | |||||||
| chr11:95787430 | T | C | 1 | a0001c0001t0001g0084 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.207+194A>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 3/9 | chr11 | 95787430 | |||||||
| chr11:95787431 | G | T | 1 | a0001c0002t0001g0087 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.207+193C>A | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 3/9 | chr11 | 95787431 | |||||||
| chr11:95787482 | C | A | 1 | a0001c0001t0001g0085 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.207+142G>T | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 3/9 | chr11 | 95787482 | |||||||
| chr11:95787531 | T | C | 102 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0010 others(99): Show |
249 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(246): Show |
intron_variant | MODIFIER | c.207+93A>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 3/9 | chr11 | 95787531 | |||||||
| chr11:95787545 | T | C | 33 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0013 others(30): Show |
75 | HG00323.hp2 HG00423.hp1 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.207+79A>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 3/9 | chr11 | 95787545 | |||||||
| chr11:95787780 | T | A | 1 | a0001c0001t0001g0132 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.153-102A>T | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 2/9 | chr11 | 95787780 | |||||||
| chr11:95787788 | G | A | 1 | a0001c0001t0001g0041 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.153-110C>T | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 2/9 | chr11 | 95787788 | |||||||
| chr11:95787851 | T | C | 14 | a0001c0001t0001g0010 a0001c0001t0001g0040 a0001c0001t0001g0041 others(11): Show |
24 | HG01081.hp1 HG01167.hp1 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.153-173A>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 2/9 | chr11 | 95787851 | |||||||
| chr11:95787880 | A | G | 45 | a0001c0001t0001g0010 a0001c0001t0001g0040 a0001c0001t0001g0041 others(42): Show |
125 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(122): Show |
intron_variant | MODIFIER | c.153-202T>C | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 2/9 | chr11 | 95787880 | |||||||
| chr11:95788156 | G | T | 1 | a0001c0002t0001g0086 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.152+343C>A | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 2/9 | chr11 | 95788156 | |||||||
| chr11:95788211 | T | G | 54 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0011 others(51): Show |
116 | HG00323.hp2 HG00423.hp1 HG00558.hp1 others(113): Show |
intron_variant | MODIFIER | c.152+288A>C | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 2/9 | chr11 | 95788211 | |||||||
| chr11:95788276 | T | A | 1 | a0001c0001t0001g0133 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.152+223A>T | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 2/9 | chr11 | 95788276 | |||||||
| chr11:95788332 | T | C | 1 | a0001c0001t0002g0153 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.152+167A>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 2/9 | chr11 | 95788332 | |||||||
| chr11:95788484 | A | G | 103 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0010 others(100): Show |
250 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(247): Show |
intron_variant | MODIFIER | c.152+15T>C | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 2/9 | chr11 | 95788484 | |||||||
| chr11:95788763 | T | G | 1 | a0001c0001t0002g0154 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.88-200A>C | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 1/9 | chr11 | 95788763 | |||||||
| chr11:95788789 | A | G | 31 | a0001c0001t0002g0001 a0001c0001t0002g0012 a0001c0001t0002g0027 others(28): Show |
101 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(98): Show |
intron_variant | MODIFIER | c.88-226T>C | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 1/9 | chr11 | 95788789 | |||||||
| chr11:95789054 | AGAAAACC others(5): Show |
A | 1 | a0001c0001t0001g0123 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.87+326_87+337delAT others(10): Show |
FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 1/9 | chr11 | 95789054 | |||||||
| chr11:95789089 | C | T | 1 | a0001c0001t0002g0135 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.87+303G>A | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 1/9 | chr11 | 95789089 | |||||||
| chr11:95789175 | G | A | 1 | a0001c0001t0001g0123 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.87+217C>T | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 1/9 | chr11 | 95789175 | |||||||
| chr11:95789265 | G | A | 1 | a0001c0002t0001g0124 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.87+127C>T | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 1/9 | chr11 | 95789265 | |||||||
| chr11:95789304 | G | A | 14 | a0001c0001t0001g0010 a0001c0001t0001g0040 a0001c0001t0001g0041 others(11): Show |
24 | HG01081.hp1 HG01167.hp1 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.87+88C>T | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 1/9 | chr11 | 95789304 |