Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 619208 |
| ensemblid | ENSG00000203778.8 |
| hgncid | 33858 |
| symbol | FAM229B |
| name | family with sequence similarity 229 member B |
| refseq_nuc | NM_001033564.3 |
| refseq_prot | NP_001028736.1 |
| ensembl_nuc | ENST00000368656.7 |
| ensembl_prot | ENSP00000357645.2 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 112087591 |
| end | 112102790 |
| strand | + |
| ver | v1.2 |
| region | chr6:112087591-112102790 |
| region5000 | chr6:112082591-112107790 |
| regionname0 | FAM229B_chr6_112087591_112102790 |
| regionname5000 | FAM229B_chr6_112082591_112107790 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 80 | 405 | 86 | 69 | 193 | 13 | 42 | 148 | FAM229B_chr6_112082591_112107790 | FAM229B | MPFQF others(75): Show |
chr6 | 112082591 | 112107790 |
| a0002 | 0/0 | 80 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | MPFQC others(75): Show |
chr6 | 112082591 | 112107790 |
| a0003 | 0/0 | 80 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | MPFQF others(75): Show |
chr6 | 112082591 | 112107790 |
| a0004 | 0/0 | 80 | 3 | 0 | 0 | 3 | 0 | 0 | 2 | FAM229B_chr6_112082591_112107790 | FAM229B | MPFQF others(75): Show |
chr6 | 112082591 | 112107790 |
| a0005 | 0/0 | 80 | 2 | 0 | 1 | 0 | 1 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | MPFQF others(75): Show |
chr6 | 112082591 | 112107790 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 240 | 405 | 86 | 69 | 193 | 13 | 42 | FAM229B_chr6_112082591_112107790 | FAM229B | ATGCC others(235): Show |
chr6 | 112082591 | 112107790 | ||
| a0002c0002 | 0/0 | 240 | 5 | 5 | 0 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | ATGCC others(235): Show |
chr6 | 112082591 | 112107790 | ||
| a0003c0004 | 0/0 | 240 | 3 | 3 | 0 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | ATGCC others(235): Show |
chr6 | 112082591 | 112107790 | ||
| a0004c0003 | 0/0 | 240 | 3 | 0 | 0 | 3 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | ATGCC others(235): Show |
chr6 | 112082591 | 112107790 | ||
| a0005c0005 | 0/0 | 240 | 2 | 0 | 1 | 0 | 1 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | ATGCC others(235): Show |
chr6 | 112082591 | 112107790 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2551 | 169 | 13 | 34 | 88 | 6 | 26 | FAM229B_chr6_112082591_112107790 | FAM229B | GTCAG others(2546): Show |
chr6 | 112082591 | 112107790 |
| a0001c0001t0002 | 0/0 | 2552 | 99 | 14 | 14 | 59 | 3 | 9 | FAM229B_chr6_112082591_112107790 | FAM229B | GTCAG others(2547): Show |
chr6 | 112082591 | 112107790 |
| a0001c0001t0003 | 0/0 | 2551 | 62 | 13 | 17 | 24 | 4 | 4 | FAM229B_chr6_112082591_112107790 | FAM229B | GTCAG others(2546): Show |
chr6 | 112082591 | 112107790 |
| a0001c0001t0004 | 0/0 | 2551 | 36 | 17 | 2 | 14 | 0 | 3 | FAM229B_chr6_112082591_112107790 | FAM229B | GTCAG others(2546): Show |
chr6 | 112082591 | 112107790 |
| a0001c0001t0005 | 0/0 | 2551 | 14 | 14 | 0 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | GTCAG others(2546): Show |
chr6 | 112082591 | 112107790 |
| a0001c0001t0006 | 0/0 | 2552 | 5 | 5 | 0 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | GTCAG others(2547): Show |
chr6 | 112082591 | 112107790 |
| a0001c0001t0007 | 0/0 | 2544 | 3 | 2 | 1 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | GTCAG others(2539): Show |
chr6 | 112082591 | 112107790 |
| a0001c0001t0008 | 0/0 | 2551 | 3 | 0 | 0 | 3 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | GTCAG others(2546): Show |
chr6 | 112082591 | 112107790 |
| a0001c0001t0009 | 0/0 | 2551 | 2 | 0 | 0 | 2 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | GTCAG others(2546): Show |
chr6 | 112082591 | 112107790 |
| a0001c0001t0010 | 0/0 | 2551 | 2 | 2 | 0 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | GTCAG others(2546): Show |
chr6 | 112082591 | 112107790 |
| a0001c0001t0012 | 0/0 | 2552 | 1 | 1 | 0 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | GTCAG others(2547): Show |
chr6 | 112082591 | 112107790 |
| a0001c0001t0013 | 0/0 | 2551 | 1 | 0 | 0 | 1 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | GTCAG others(2546): Show |
chr6 | 112082591 | 112107790 |
| a0001c0001t0014 | 0/0 | 2552 | 1 | 1 | 0 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | GTCAG others(2547): Show |
chr6 | 112082591 | 112107790 |
| a0001c0001t0015 | 0/0 | 2552 | 1 | 1 | 0 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | GTCAG others(2547): Show |
chr6 | 112082591 | 112107790 |
| a0001c0001t0017 | 0/0 | 2551 | 1 | 0 | 0 | 1 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | GTCAG others(2546): Show |
chr6 | 112082591 | 112107790 |
| a0001c0001t0018 | 0/0 | 2551 | 1 | 0 | 0 | 1 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | GTCAG others(2546): Show |
chr6 | 112082591 | 112107790 |
| a0001c0001t0019 | 0/0 | 2551 | 1 | 1 | 0 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | GTCAG others(2546): Show |
chr6 | 112082591 | 112107790 |
| a0001c0001t0020 | 0/0 | 2551 | 1 | 1 | 0 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | GTCAG others(2546): Show |
chr6 | 112082591 | 112107790 |
| a0001c0001t0021 | 0/0 | 2551 | 1 | 0 | 1 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | GTCAG others(2546): Show |
chr6 | 112082591 | 112107790 |
| a0001c0001t0022 | 0/0 | 2551 | 1 | 1 | 0 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | GTCAG others(2546): Show |
chr6 | 112082591 | 112107790 |
| a0002c0002t0001 | 0/0 | 2551 | 5 | 5 | 0 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | GTCAG others(2546): Show |
chr6 | 112082591 | 112107790 |
| a0003c0004t0011 | 0/0 | 2551 | 2 | 2 | 0 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | GTCAG others(2546): Show |
chr6 | 112082591 | 112107790 |
| a0003c0004t0016 | 0/0 | 2551 | 1 | 1 | 0 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | GTCAG others(2546): Show |
chr6 | 112082591 | 112107790 |
| a0004c0003t0001 | 0/0 | 2551 | 1 | 0 | 0 | 1 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | GTCAG others(2546): Show |
chr6 | 112082591 | 112107790 |
| a0004c0003t0003 | 0/0 | 2551 | 2 | 0 | 0 | 2 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | GTCAG others(2546): Show |
chr6 | 112082591 | 112107790 |
| a0005c0005t0001 | 0/0 | 2551 | 2 | 0 | 1 | 0 | 1 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | GTCAG others(2546): Show |
chr6 | 112082591 | 112107790 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 1/1 | 87 | 2 | 20 | 48 | 2 | 13 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| a0001c0001t0001g0005 | 0/0 | 26 | 0 | 6 | 12 | 2 | 6 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| a0001c0001t0001g0007 | 0/0 | 9 | 0 | 1 | 8 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| a0001c0001t0001g0008 | 0/0 | 9 | 9 | 0 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| a0001c0001t0001g0012 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| a0001c0001t0001g0015 | 0/0 | 5 | 0 | 3 | 0 | 2 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| a0001c0001t0001g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| a0001c0001t0002g0002 | 0/0 | 45 | 11 | 10 | 16 | 3 | 5 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| a0001c0001t0002g0004 | 0/0 | 35 | 0 | 0 | 31 | 0 | 4 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| a0001c0001t0002g0013 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| a0001c0001t0002g0022 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| a0001c0001t0002g0023 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| a0001c0001t0003g0003 | 0/0 | 36 | 9 | 7 | 15 | 2 | 3 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| a0001c0001t0003g0009 | 0/0 | 9 | 1 | 6 | 0 | 2 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| a0001c0001t0003g0010 | 0/0 | 8 | 0 | 4 | 4 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| a0001c0001t0003g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| a0001c0001t0003g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| a0001c0001t0003g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| a0001c0001t0003g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| a0001c0001t0003g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| a0001c0001t0003g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| a0001c0001t0003g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| a0001c0001t0004g0006 | 0/0 | 23 | 13 | 0 | 8 | 0 | 2 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| a0001c0001t0004g0014 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| a0001c0001t0004g0018 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| a0001c0001t0004g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| a0001c0001t0004g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| a0001c0001t0004g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| a0001c0001t0004g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| a0001c0001t0005g0011 | 0/0 | 8 | 8 | 0 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| a0001c0001t0005g0016 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| a0001c0001t0005g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| a0001c0001t0006g0017 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| a0001c0001t0007g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| a0001c0001t0007g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| a0001c0001t0007g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| a0001c0001t0008g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| a0001c0001t0008g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| a0001c0001t0009g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| a0001c0001t0010g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| a0001c0001t0012g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| a0001c0001t0013g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| a0001c0001t0014g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| a0001c0001t0015g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| a0001c0001t0017g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| a0001c0001t0018g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| a0001c0001t0019g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| a0001c0001t0020g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| a0001c0001t0021g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| a0001c0001t0022g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| a0002c0002t0001g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| a0002c0002t0001g0019 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| a0003c0004t0011g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| a0003c0004t0016g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| a0004c0003t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| a0004c0003t0003g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| a0005c0005t0001g0001 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0003 | g0009 | EUR | GBR | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0002 | EUR | GBR | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | GBR | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG00140 | hp2 | a0001 | c0001 | t0003 | g0003 | EUR | GBR | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0002 | EUR | FIN | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0005 | EUR | FIN | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG00408 | hp1 | a0001 | c0001 | t0004 | g0050 | EAS | CHS | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG00438 | hp2 | a0001 | c0001 | t0004 | g0014 | EAS | CHS | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG00544 | hp1 | a0001 | c0001 | t0004 | g0006 | EAS | CHS | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | CHS | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | CHS | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG00597 | hp2 | a0001 | c0001 | t0017 | g0005 | EAS | CHS | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG00609 | hp1 | a0001 | c0001 | t0008 | g0064 | EAS | CHS | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | CHS | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG00621 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | CHS | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | CHS | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG00741 | hp2 | a0001 | c0001 | t0004 | g0039 | AMR | PUR | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG01070 | hp1 | a0001 | c0001 | t0003 | g0003 | AMR | PUR | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG01071 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | PUR | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG01081 | hp1 | a0001 | c0001 | t0004 | g0018 | AMR | PUR | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0022 | AMR | PUR | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG01167 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | PUR | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG01168 | hp1 | a0001 | c0001 | t0003 | g0009 | AMR | PUR | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG01169 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | PUR | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG01175 | hp1 | a0001 | c0001 | t0003 | g0009 | AMR | PUR | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0057 | AMR | PUR | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG01192 | hp2 | a0001 | c0001 | t0003 | g0009 | AMR | PUR | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG01243 | hp1 | a0001 | c0001 | t0007 | g0060 | AMR | PUR | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0022 | AMR | CLM | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0022 | AMR | CLM | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG01346 | hp1 | a0001 | c0001 | t0003 | g0009 | AMR | CLM | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0066 | AMR | CLM | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | CLM | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG01358 | hp2 | a0001 | c0001 | t0003 | g0009 | AMR | CLM | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG01361 | hp1 | a0001 | c0001 | t0003 | g0009 | AMR | CLM | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG01433 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | CLM | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG01496 | hp1 | a0001 | c0001 | t0003 | g0003 | AMR | CLM | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0015 | EUR | IBS | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0015 | EUR | IBS | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG01884 | hp2 | a0002 | c0002 | t0001 | g0019 | AFR | ACB | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0023 | AFR | ACB | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG01891 | hp2 | a0001 | c0001 | t0005 | g0016 | AFR | ACB | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG01934 | hp2 | a0001 | c0001 | t0003 | g0010 | AMR | PEL | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG01943 | hp2 | a0001 | c0001 | t0003 | g0010 | AMR | PEL | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG01952 | hp1 | a0001 | c0001 | t0003 | g0010 | AMR | PEL | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG02004 | hp1 | a0005 | c0005 | t0001 | g0001 | AMR | PEL | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG02004 | hp2 | a0001 | c0001 | t0021 | g0010 | AMR | PEL | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | KHV | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | KHV | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG02040 | hp2 | a0001 | c0001 | t0004 | g0014 | EAS | KHV | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG02055 | hp1 | a0001 | c0001 | t0004 | g0006 | AFR | ACB | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG02055 | hp2 | a0003 | c0004 | t0011 | g0024 | AFR | ACB | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | KHV | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG02071 | hp1 | a0001 | c0001 | t0004 | g0006 | EAS | KHV | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG02074 | hp1 | a0001 | c0001 | t0008 | g0003 | EAS | KHV | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | KHV | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | KHV | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | KHV | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | KHV | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG02129 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | KHV | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG02132 | hp1 | a0001 | c0001 | t0004 | g0006 | EAS | KHV | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG02132 | hp2 | a0001 | c0001 | t0004 | g0014 | EAS | KHV | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | ACB | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG02145 | hp2 | a0001 | c0001 | t0003 | g0003 | AFR | ACB | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG02155 | hp2 | a0004 | c0003 | t0001 | g0007 | EAS | CDX | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CDX | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | ACB | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG02257 | hp2 | a0001 | c0001 | t0005 | g0016 | AFR | ACB | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG02258 | hp1 | a0001 | c0001 | t0003 | g0003 | AFR | ACB | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG02280 | hp1 | a0001 | c0001 | t0022 | g0003 | AFR | ACB | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG02280 | hp2 | a0001 | c0001 | t0004 | g0006 | AFR | ACB | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG02300 | hp2 | a0001 | c0001 | t0003 | g0010 | AMR | PEL | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG02523 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | KHV | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | KHV | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG02572 | hp1 | a0001 | c0001 | t0003 | g0003 | AFR | GWD | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG02572 | hp2 | a0001 | c0001 | t0005 | g0011 | AFR | GWD | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG02615 | hp2 | a0001 | c0001 | t0005 | g0011 | AFR | GWD | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | GWD | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG02622 | hp2 | a0001 | c0001 | t0007 | g0061 | AFR | GWD | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG02630 | hp1 | a0001 | c0001 | t0005 | g0059 | AFR | GWD | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG02647 | hp1 | a0001 | c0001 | t0006 | g0017 | AFR | GWD | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG02647 | hp2 | a0001 | c0001 | t0004 | g0006 | AFR | GWD | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG02717 | hp1 | a0001 | c0001 | t0004 | g0006 | AFR | GWD | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG02717 | hp2 | a0001 | c0001 | t0003 | g0003 | AFR | GWD | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG02723 | hp1 | a0001 | c0001 | t0004 | g0006 | AFR | GWD | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG02723 | hp2 | a0001 | c0001 | t0004 | g0018 | AFR | GWD | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0026 | SAS | PJL | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | GWD | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG02809 | hp2 | a0001 | c0001 | t0015 | g0002 | AFR | GWD | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | GWD | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG02886 | hp1 | a0001 | c0001 | t0010 | g0025 | AFR | GWD | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG02886 | hp2 | a0001 | c0001 | t0005 | g0011 | AFR | GWD | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG02895 | hp1 | a0001 | c0001 | t0006 | g0017 | AFR | GWD | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0023 | AFR | GWD | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG02896 | hp2 | a0001 | c0001 | t0004 | g0006 | AFR | GWD | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG02897 | hp1 | a0001 | c0001 | t0004 | g0006 | AFR | GWD | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0023 | AFR | GWD | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG02922 | hp1 | a0001 | c0001 | t0005 | g0011 | AFR | ESN | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG02922 | hp2 | a0001 | c0001 | t0004 | g0006 | AFR | ESN | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG02970 | hp1 | a0001 | c0001 | t0006 | g0017 | AFR | ESN | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG02970 | hp2 | a0001 | c0001 | t0003 | g0003 | AFR | ESN | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG02976 | hp1 | a0001 | c0001 | t0007 | g0062 | AFR | ESN | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | ESN | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0004 | SAS | PJL | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG03130 | hp2 | a0001 | c0001 | t0003 | g0038 | AFR | ESN | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0052 | AFR | ESN | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG03139 | hp2 | a0001 | c0001 | t0003 | g0037 | AFR | ESN | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG03195 | hp1 | a0001 | c0001 | t0005 | g0016 | AFR | ESN | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG03195 | hp2 | a0001 | c0001 | t0019 | g0040 | AFR | ESN | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG03209 | hp1 | a0002 | c0002 | t0001 | g0019 | AFR | MSL | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG03209 | hp2 | a0001 | c0001 | t0003 | g0009 | AFR | MSL | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG03225 | hp1 | a0001 | c0001 | t0004 | g0006 | AFR | MSL | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG03225 | hp2 | a0001 | c0001 | t0005 | g0016 | AFR | MSL | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG03239 | hp2 | a0001 | c0001 | t0003 | g0003 | SAS | PJL | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG03453 | hp1 | a0001 | c0001 | t0004 | g0006 | AFR | MSL | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG03453 | hp2 | a0001 | c0001 | t0012 | g0002 | AFR | MSL | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG03486 | hp1 | a0001 | c0001 | t0010 | g0025 | AFR | MSL | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG03486 | hp2 | a0001 | c0001 | t0004 | g0006 | AFR | MSL | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG03490 | hp2 | a0001 | c0001 | t0003 | g0003 | SAS | PJL | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG03516 | hp1 | a0001 | c0001 | t0006 | g0017 | AFR | ESN | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG03516 | hp2 | a0001 | c0001 | t0004 | g0006 | AFR | ESN | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | GWD | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG03579 | hp1 | a0001 | c0001 | t0004 | g0018 | AFR | MSL | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG03579 | hp2 | a0001 | c0001 | t0020 | g0003 | AFR | MSL | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | STU | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0004 | SAS | BEB | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG03831 | hp2 | a0001 | c0001 | t0004 | g0006 | SAS | BEB | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0004 | SAS | BEB | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG03834 | hp2 | a0001 | c0001 | t0003 | g0054 | SAS | BEB | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | BEB | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG03927 | hp2 | a0001 | c0001 | t0004 | g0042 | SAS | BEB | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0030 | SAS | BEB | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | STU | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG04184 | hp1 | a0001 | c0001 | t0003 | g0003 | SAS | BEB | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0030 | SAS | BEB | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0004 | SAS | STU | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0051 | SAS | STU | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG04228 | hp2 | a0001 | c0001 | t0004 | g0006 | SAS | STU | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA18522 | hp1 | a0001 | c0001 | t0005 | g0016 | AFR | YRI | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA18522 | hp2 | a0001 | c0001 | t0005 | g0011 | AFR | YRI | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA18747 | hp1 | a0001 | c0001 | t0008 | g0003 | EAS | CHB | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | YRI | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA18906 | hp2 | a0001 | c0001 | t0004 | g0006 | AFR | YRI | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA18939 | hp1 | a0001 | c0001 | t0018 | g0031 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA18940 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA18946 | hp1 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA18947 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA18948 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA18948 | hp2 | a0001 | c0001 | t0013 | g0001 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA18949 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA18951 | hp2 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA18952 | hp1 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA18954 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA18959 | hp2 | a0004 | c0003 | t0003 | g0003 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA18960 | hp2 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA18963 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA18965 | hp2 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA18968 | hp2 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA18969 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA18971 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA18971 | hp2 | a0001 | c0001 | t0003 | g0021 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA18972 | hp2 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA18977 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA18981 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA18985 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA18988 | hp1 | a0001 | c0001 | t0004 | g0014 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA18991 | hp2 | a0001 | c0001 | t0004 | g0014 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA18992 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA18993 | hp1 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA19005 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA19006 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | LWK | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | LWK | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA19043 | hp1 | a0002 | c0002 | t0001 | g0001 | AFR | LWK | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | LWK | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA19055 | hp1 | a0001 | c0001 | t0003 | g0053 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA19056 | hp2 | a0001 | c0001 | t0009 | g0001 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA19062 | hp1 | a0001 | c0001 | t0003 | g0021 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA19064 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA19067 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA19068 | hp2 | a0001 | c0001 | t0003 | g0031 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA19075 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA19076 | hp1 | a0004 | c0003 | t0003 | g0003 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA19076 | hp2 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA19077 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA19080 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA19083 | hp1 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA19083 | hp2 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA19085 | hp2 | a0001 | c0001 | t0009 | g0001 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA19090 | hp1 | a0001 | c0001 | t0003 | g0021 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA19240 | hp1 | a0001 | c0001 | t0005 | g0011 | AFR | YRI | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA19240 | hp2 | a0002 | c0002 | t0001 | g0019 | AFR | YRI | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA20129 | hp1 | a0001 | c0001 | t0006 | g0017 | AFR | ASW | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | ASW | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA20752 | hp1 | a0005 | c0005 | t0001 | g0001 | EUR | TSI | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA20752 | hp2 | a0001 | c0001 | t0003 | g0003 | EUR | TSI | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA20805 | hp1 | a0001 | c0001 | t0003 | g0009 | EUR | TSI | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0002 | EUR | TSI | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0046 | SAS | GIH | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG01123 | hp1 | a0001 | c0001 | t0003 | g0003 | AMR | CLM | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG02109 | hp1 | a0003 | c0004 | t0011 | g0024 | AFR | ACB | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG02109 | hp2 | a0001 | c0001 | t0003 | g0003 | AFR | ACB | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG02486 | hp1 | a0001 | c0001 | t0003 | g0003 | AFR | ACB | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG02486 | hp2 | a0002 | c0002 | t0001 | g0019 | AFR | ACB | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG02559 | hp1 | a0001 | c0001 | t0004 | g0044 | AFR | ACB | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG02559 | hp2 | a0001 | c0001 | t0003 | g0003 | AFR | ACB | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG03471 | hp1 | a0001 | c0001 | t0014 | g0036 | AFR | MSL | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG03471 | hp2 | a0001 | c0001 | t0005 | g0011 | AFR | MSL | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | USA | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| HG06807 | hp2 | a0001 | c0001 | t0003 | g0003 | AFR | USA | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA20300 | hp1 | a0001 | c0001 | t0004 | g0018 | AFR | USA | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA20300 | hp2 | a0003 | c0004 | t0016 | g0032 | AFR | USA | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | LWK | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| NA21309 | hp2 | a0001 | c0001 | t0005 | g0011 | AFR | LWK | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0001 | REF | REF | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0001 | REF | REF | FAM229B_chr6_112082591_112107790 | FAM229B | chr6 | 112082591 | 112107790 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:112099297 | T | G | 1 | a0002 | 5 | HG01884.hp2 HG02486.hp2 HG03209.hp1 others(2): Show |
missense_variant | MODERATE | c.14T>G | p.Phe5Cys | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 3/4 | 319/2551 | 14/243 | 5/80 | chr6 | 112099297 | |||
| chr6:112099312 | G | A | 1 | a0005 | 2 | HG02004.hp1 NA20752.hp1 |
missense_variant | MODERATE | c.29G>A | p.Arg10Lys | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 3/4 | 334/2551 | 29/243 | 10/80 | chr6 | 112099312 | |||
| chr6:112100722 | G | A | 1 | a0004 | 3 | HG02155.hp2 NA18959.hp2 NA19076.hp1 |
missense_variant | MODERATE | c.178G>A | p.Val60Ile | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 4/4 | 483/2551 | 178/243 | 60/80 | chr6 | 112100722 | |||
| chr6:112100731 | T | A | 1 | a0003 | 3 | HG02055.hp2 HG02109.hp1 NA20300.hp2 |
missense_variant | MODERATE | c.187T>A | p.Tyr63Asn | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 4/4 | 492/2551 | 187/243 | 63/80 | chr6 | 112100731 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:112097055 | T | C | 1 | a0001c0001t0012 | 1 | HG03453.hp2 | 5_prime_UTR_variant | MODIFIER | c.-161T>C | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 2/4 | 2229 | chr6 | 112097055 | ||||||
| chr6:112097086 | G | A | 1 | a0001c0001t0004 | 36 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(33): Show |
5_prime_UTR_variant | MODIFIER | c.-130G>A | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 2/4 | 2198 | chr6 | 112097086 | ||||||
| chr6:112099276 | A | G | 1 | a0001c0001t0022 | 1 | HG02280.hp1 | 5_prime_UTR_variant | MODIFIER | c.-8A>G | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 3/4 | 8 | chr6 | 112099276 | ||||||
| chr6:112100824 | A | G | 1 | a0003c0004t0011 | 2 | HG02055.hp2 HG02109.hp1 |
3_prime_UTR_variant | MODIFIER | c.*37A>G | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 4/4 | 37 | chr6 | 112100824 | ||||||
| chr6:112100901 | G | A | 1 | a0001c0001t0013 | 1 | NA18948.hp2 | 3_prime_UTR_variant | MODIFIER | c.*114G>A | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 4/4 | 114 | chr6 | 112100901 | ||||||
| chr6:112100924 | C | T | 1 | a0001c0001t0021 | 1 | HG02004.hp2 | 3_prime_UTR_variant | MODIFIER | c.*137C>T | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 4/4 | 137 | chr6 | 112100924 | ||||||
| chr6:112100951 | T | C | 6 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0007 others(3): Show |
110 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(107): Show |
3_prime_UTR_variant | MODIFIER | c.*164T>C | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 4/4 | 164 | chr6 | 112100951 | ||||||
| chr6:112100980 | T | C | 1 | a0001c0001t0014 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*193T>C | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 4/4 | 193 | chr6 | 112100980 | ||||||
| chr6:112101018 | C | T | 1 | a0001c0001t0008 | 3 | HG00609.hp1 HG02074.hp1 NA18747.hp1 |
3_prime_UTR_variant | MODIFIER | c.*231C>T | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 4/4 | 231 | chr6 | 112101018 | ||||||
| chr6:112101159 | TGCTACTT others(1): Show |
T | 1 | a0001c0001t0007 | 3 | HG01243.hp1 HG02622.hp2 HG02976.hp1 |
3_prime_UTR_variant | MODIFIER | c.*377_*384delCTTGGC others(2): Show |
FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 4/4 | 377 | INFO_REALIGN_3_PRIME | chr6 | 112101159 | |||||
| chr6:112101187 | G | T | 1 | a0001c0001t0020 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*400G>T | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 4/4 | 400 | chr6 | 112101187 | ||||||
| chr6:112101206 | T | A | 1 | a0001c0001t0009 | 2 | NA19056.hp2 NA19085.hp2 |
3_prime_UTR_variant | MODIFIER | c.*419T>A | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 4/4 | 419 | chr6 | 112101206 | ||||||
| chr6:112101365 | C | G | 1 | a0001c0001t0019 | 1 | HG03195.hp2 | 3_prime_UTR_variant | MODIFIER | c.*578C>G | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 4/4 | 578 | chr6 | 112101365 | ||||||
| chr6:112101444 | T | C | 10 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0006 others(7): Show |
128 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(125): Show |
3_prime_UTR_variant | MODIFIER | c.*657T>C | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 4/4 | 657 | chr6 | 112101444 | ||||||
| chr6:112101461 | A | C | 10 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0006 others(7): Show |
128 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(125): Show |
3_prime_UTR_variant | MODIFIER | c.*674A>C | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 4/4 | 674 | chr6 | 112101461 | ||||||
| chr6:112101595 | T | C | 1 | a0001c0001t0015 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*808T>C | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 4/4 | 808 | chr6 | 112101595 | ||||||
| chr6:112101613 | A | G | 1 | a0001c0001t0005 | 14 | HG01891.hp2 HG02257.hp2 HG02572.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*826A>G | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 4/4 | 826 | chr6 | 112101613 | ||||||
| chr6:112101638 | G | A | 1 | a0001c0001t0017 | 1 | HG00597.hp2 | 3_prime_UTR_variant | MODIFIER | c.*851G>A | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 4/4 | 851 | chr6 | 112101638 | ||||||
| chr6:112101710 | A | G | 1 | a0003c0004t0016 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*923A>G | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 4/4 | 923 | chr6 | 112101710 | ||||||
| chr6:112101824 | G | A | 1 | a0001c0001t0018 | 1 | NA18939.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1037G>A | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 4/4 | 1037 | chr6 | 112101824 | ||||||
| chr6:112102003 | G | A | 4 | a0001c0001t0005 a0001c0001t0019 a0003c0004t0011 others(1): Show |
18 | HG01891.hp2 HG02055.hp2 HG02109.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*1216G>A | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 4/4 | 1216 | chr6 | 112102003 | ||||||
| chr6:112102059 | G | C | 6 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0007 others(3): Show |
110 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(107): Show |
3_prime_UTR_variant | MODIFIER | c.*1272G>C | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 4/4 | 1272 | chr6 | 112102059 | ||||||
| chr6:112102079 | T | C | 1 | a0001c0001t0014 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1292T>C | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 4/4 | 1292 | chr6 | 112102079 | ||||||
| chr6:112102195 | C | T | 1 | a0003c0004t0016 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1408C>T | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 4/4 | 1408 | chr6 | 112102195 | ||||||
| chr6:112102281 | C | T | 1 | a0001c0001t0014 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1494C>T | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 4/4 | 1494 | chr6 | 112102281 | ||||||
| chr6:112102312 | C | T | 1 | a0001c0001t0010 | 2 | HG02886.hp1 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1525C>T | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 4/4 | 1525 | chr6 | 112102312 | ||||||
| chr6:112102379 | G | C | 3 | a0001c0001t0002 a0001c0001t0012 a0001c0001t0015 |
101 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(98): Show |
3_prime_UTR_variant | MODIFIER | c.*1592G>C | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 4/4 | 1592 | chr6 | 112102379 | ||||||
| chr6:112102484 | C | CA | 6 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0007 others(3): Show |
110 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(107): Show |
3_prime_UTR_variant | MODIFIER | c.*1706dupA | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 4/4 | 1707 | INFO_REALIGN_3_PRIME | chr6 | 112102484 | |||||
| chr6:112102607 | A | G | 18 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(15): Show |
201 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(198): Show |
3_prime_UTR_variant | MODIFIER | c.*1820A>G | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 4/4 | 1820 | chr6 | 112102607 | ||||||
| chr6:112102640 | G | A | 1 | a0001c0001t0010 | 2 | HG02886.hp1 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1853G>A | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 4/4 | 1853 | chr6 | 112102640 | ||||||
| chr6:112102741 | C | A | 1 | a0001c0001t0006 | 5 | HG02647.hp1 HG02895.hp1 HG02970.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1954C>A | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 4/4 | 1954 | chr6 | 112102741 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:112087778 | A | C | 1 | a0001c0001t0002g0067 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.-176+58A>C | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112087778 | |||||||
| chr6:112087805 | C | T | 1 | a0001c0001t0001g0066 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-176+85C>T | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112087805 | |||||||
| chr6:112087909 | T | C | 2 | a0003c0004t0011g0024 a0003c0004t0016g0032 |
3 | HG02055.hp2 HG02109.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-176+189T>C | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112087909 | |||||||
| chr6:112087991 | A | G | 1 | a0001c0001t0002g0023 | 3 | HG01891.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-176+271A>G | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112087991 | |||||||
| chr6:112088027 | G | T | 1 | a0001c0001t0001g0065 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-176+307G>T | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112088027 | |||||||
| chr6:112088066 | G | C | 5 | a0001c0001t0001g0007 a0001c0001t0001g0033 a0001c0001t0001g0034 others(2): Show |
13 | HG01433.hp1 HG02027.hp2 HG02056.hp1 others(10): Show |
intron_variant | MODIFIER | c.-176+346G>C | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112088066 | |||||||
| chr6:112088095 | T | C | 1 | a0001c0001t0014g0036 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-176+375T>C | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112088095 | |||||||
| chr6:112088149 | T | G | 2 | a0001c0001t0003g0037 a0001c0001t0003g0038 |
2 | HG03130.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-176+429T>G | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112088149 | |||||||
| chr6:112088269 | T | G | 1 | a0001c0001t0004g0039 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-176+549T>G | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112088269 | |||||||
| chr6:112088421 | T | C | 2 | a0003c0004t0011g0024 a0003c0004t0016g0032 |
3 | HG02055.hp2 HG02109.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-176+701T>C | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112088421 | |||||||
| chr6:112088600 | C | T | 1 | a0001c0001t0008g0064 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-176+880C>T | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112088600 | |||||||
| chr6:112088601 | G | A | 3 | a0001c0001t0019g0040 a0003c0004t0011g0024 a0003c0004t0016g0032 |
4 | HG02055.hp2 HG02109.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-176+881G>A | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112088601 | |||||||
| chr6:112088810 | G | A | 1 | a0003c0004t0011g0024 | 2 | HG02055.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.-176+1090G>A | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112088810 | |||||||
| chr6:112088908 | C | G | 1 | a0001c0001t0006g0017 | 5 | HG02647.hp1 HG02895.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.-176+1188C>G | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112088908 | |||||||
| chr6:112088922 | G | T | 1 | a0001c0001t0003g0038 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-176+1202G>T | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112088922 | |||||||
| chr6:112088946 | A | C | 1 | a0001c0001t0002g0063 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.-176+1226A>C | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112088946 | |||||||
| chr6:112089076 | T | C | 1 | a0001c0001t0014g0036 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-176+1356T>C | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112089076 | |||||||
| chr6:112089133 | A | G | 20 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0013 others(17): Show |
123 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(120): Show |
intron_variant | MODIFIER | c.-176+1413A>G | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112089133 | |||||||
| chr6:112089283 | A | G | 3 | a0001c0001t0019g0040 a0003c0004t0011g0024 a0003c0004t0016g0032 |
4 | HG02055.hp2 HG02109.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-176+1563A>G | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112089283 | |||||||
| chr6:112089388 | G | GA | 16 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0013 others(13): Show |
115 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.-176+1672dupA | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr6 | 112089388 | ||||||
| chr6:112089529 | A | G | 2 | a0003c0004t0011g0024 a0003c0004t0016g0032 |
3 | HG02055.hp2 HG02109.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-176+1809A>G | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112089529 | |||||||
| chr6:112089656 | G | T | 2 | a0001c0001t0003g0010 a0001c0001t0021g0010 |
9 | HG01934.hp2 HG01943.hp2 HG01952.hp1 others(6): Show |
intron_variant | MODIFIER | c.-176+1936G>T | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112089656 | |||||||
| chr6:112089825 | A | G | 1 | a0001c0001t0007g0062 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-176+2105A>G | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112089825 | |||||||
| chr6:112089830 | C | T | 3 | a0001c0001t0005g0011 a0001c0001t0005g0016 a0001c0001t0005g0059 |
14 | HG01891.hp2 HG02257.hp2 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.-176+2110C>T | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112089830 | |||||||
| chr6:112089857 | C | T | 1 | a0001c0001t0019g0040 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-176+2137C>T | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112089857 | |||||||
| chr6:112089871 | A | G | 14 | a0001c0001t0003g0003 a0001c0001t0003g0009 a0001c0001t0003g0010 others(11): Show |
68 | HG00099.hp1 HG00140.hp2 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.-176+2151A>G | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112089871 | |||||||
| chr6:112089979 | G | C | 3 | a0001c0001t0005g0011 a0001c0001t0005g0016 a0001c0001t0005g0059 |
14 | HG01891.hp2 HG02257.hp2 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.-176+2259G>C | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112089979 | |||||||
| chr6:112090047 | A | G | 17 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0013 others(14): Show |
109 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.-176+2327A>G | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112090047 | |||||||
| chr6:112090064 | A | G | 1 | a0001c0001t0003g0021 | 3 | NA18971.hp2 NA19062.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.-176+2344A>G | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112090064 | |||||||
| chr6:112090145 | G | A | 1 | a0001c0001t0004g0014 | 5 | HG00438.hp2 HG02040.hp2 HG02132.hp2 others(2): Show |
intron_variant | MODIFIER | c.-176+2425G>A | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112090145 | |||||||
| chr6:112090207 | G | GTCTA | 23 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0013 others(20): Show |
127 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(124): Show |
intron_variant | MODIFIER | c.-176+2490_-176+249 others(8): Show |
FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr6 | 112090207 | ||||||
| chr6:112090479 | G | A | 16 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0013 others(13): Show |
104 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.-176+2759G>A | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112090479 | |||||||
| chr6:112090548 | A | G | 1 | a0001c0001t0001g0008 | 9 | HG01884.hp1 HG02258.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.-176+2828A>G | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112090548 | |||||||
| chr6:112090567 | ACAAT | A | 16 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0013 others(13): Show |
104 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.-176+2851_-176+285 others(8): Show |
FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr6 | 112090567 | ||||||
| chr6:112090749 | T | C | 1 | a0001c0001t0001g0041 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-176+3029T>C | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112090749 | |||||||
| chr6:112090838 | C | T | 1 | a0001c0001t0003g0052 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-176+3118C>T | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112090838 | |||||||
| chr6:112090856 | G | A | 12 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0013 others(9): Show |
98 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.-176+3136G>A | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112090856 | |||||||
| chr6:112090980 | G | T | 24 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0013 others(21): Show |
128 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.-176+3260G>T | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112090980 | |||||||
| chr6:112091000 | C | T | 6 | a0001c0001t0005g0011 a0001c0001t0005g0016 a0001c0001t0005g0059 others(3): Show |
18 | HG01891.hp2 HG02055.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.-176+3280C>T | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112091000 | |||||||
| chr6:112091017 | TC | T | 6 | a0001c0001t0005g0011 a0001c0001t0005g0016 a0001c0001t0005g0059 others(3): Show |
18 | HG01891.hp2 HG02055.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.-176+3299delC | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr6 | 112091017 | ||||||
| chr6:112091054 | CTCTACTT others(1): Show |
C | 16 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0013 others(13): Show |
104 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.-176+3336_-176+334 others(12): Show |
FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr6 | 112091054 | ||||||
| chr6:112091092 | C | A | 23 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0013 others(20): Show |
127 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(124): Show |
intron_variant | MODIFIER | c.-176+3372C>A | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112091092 | |||||||
| chr6:112091382 | T | C | 2 | a0001c0001t0004g0018 a0001c0001t0004g0042 |
5 | HG01081.hp1 HG02723.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.-176+3662T>C | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112091382 | |||||||
| chr6:112091479 | G | C | 1 | a0001c0001t0006g0017 | 5 | HG02647.hp1 HG02895.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.-176+3759G>C | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112091479 | |||||||
| chr6:112091619 | A | G | 1 | a0001c0001t0014g0036 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-176+3899A>G | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112091619 | |||||||
| chr6:112091785 | T | G | 1 | a0001c0001t0019g0040 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-176+4065T>G | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112091785 | |||||||
| chr6:112091793 | A | G | 2 | a0003c0004t0011g0024 a0003c0004t0016g0032 |
3 | HG02055.hp2 HG02109.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-176+4073A>G | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112091793 | |||||||
| chr6:112091878 | GAA | G | 12 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0013 others(9): Show |
98 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.-176+4160_-176+416 others(6): Show |
FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr6 | 112091878 | ||||||
| chr6:112091975 | G | A | 18 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0013 others(15): Show |
110 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.-176+4255G>A | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112091975 | |||||||
| chr6:112092217 | C | A | 13 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0013 others(10): Show |
101 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.-176+4497C>A | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112092217 | |||||||
| chr6:112092259 | G | A | 42 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0013 others(39): Show |
201 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(198): Show |
intron_variant | MODIFIER | c.-176+4539G>A | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112092259 | |||||||
| chr6:112092313 | T | G | 24 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0013 others(21): Show |
128 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.-176+4593T>G | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112092313 | |||||||
| chr6:112092634 | A | G | 1 | a0001c0001t0001g0051 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-175-4407A>G | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112092634 | |||||||
| chr6:112092729 | T | C | 3 | a0001c0001t0007g0060 a0001c0001t0007g0061 a0001c0001t0007g0062 |
3 | HG01243.hp1 HG02622.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-175-4312T>C | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112092729 | |||||||
| chr6:112092767 | A | C | 1 | a0001c0001t0004g0050 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-175-4274A>C | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112092767 | |||||||
| chr6:112092832 | A | G | 18 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0013 others(15): Show |
110 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.-175-4209A>G | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112092832 | |||||||
| chr6:112092842 | G | A | 18 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0013 others(15): Show |
110 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.-175-4199G>A | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112092842 | |||||||
| chr6:112092883 | A | T | 1 | a0001c0001t0003g0054 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-175-4158A>T | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112092883 | |||||||
| chr6:112093032 | A | G | 1 | a0001c0001t0019g0040 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-175-4009A>G | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112093032 | |||||||
| chr6:112093040 | G | A | 14 | a0001c0001t0003g0003 a0001c0001t0003g0009 a0001c0001t0003g0010 others(11): Show |
68 | HG00099.hp1 HG00140.hp2 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.-175-4001G>A | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112093040 | |||||||
| chr6:112093049 | A | G | 24 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0013 others(21): Show |
128 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.-175-3992A>G | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112093049 | |||||||
| chr6:112093077 | A | T | 18 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0013 others(15): Show |
110 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.-175-3964A>T | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112093077 | |||||||
| chr6:112093107 | A | C | 13 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0013 others(10): Show |
101 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.-175-3934A>C | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112093107 | |||||||
| chr6:112093222 | C | A | 1 | a0001c0001t0001g0043 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-175-3819C>A | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112093222 | |||||||
| chr6:112093251 | C | G | 1 | a0001c0001t0001g0035 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.-175-3790C>G | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112093251 | |||||||
| chr6:112093252 | A | T | 1 | a0001c0001t0001g0035 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.-175-3789A>T | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112093252 | |||||||
| chr6:112093253 | G | T | 1 | a0001c0001t0001g0035 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.-175-3788G>T | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112093253 | |||||||
| chr6:112093558 | C | T | 1 | a0001c0001t0010g0025 | 2 | HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-175-3483C>T | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112093558 | |||||||
| chr6:112093573 | G | A | 25 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0013 others(22): Show |
130 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(127): Show |
intron_variant | MODIFIER | c.-175-3468G>A | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112093573 | |||||||
| chr6:112093658 | G | A | 3 | a0001c0001t0007g0060 a0001c0001t0007g0061 a0001c0001t0007g0062 |
3 | HG01243.hp1 HG02622.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-175-3383G>A | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112093658 | |||||||
| chr6:112093687 | T | C | 1 | a0001c0001t0001g0012 | 7 | NA18947.hp2 NA18961.hp1 NA18962.hp2 others(4): Show |
intron_variant | MODIFIER | c.-175-3354T>C | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112093687 | |||||||
| chr6:112093730 | A | G | 1 | a0003c0004t0016g0032 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-175-3311A>G | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112093730 | |||||||
| chr6:112093889 | G | T | 2 | a0003c0004t0011g0024 a0003c0004t0016g0032 |
3 | HG02055.hp2 HG02109.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-175-3152G>T | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112093889 | |||||||
| chr6:112094008 | A | G | 3 | a0001c0001t0007g0060 a0001c0001t0007g0061 a0001c0001t0007g0062 |
3 | HG01243.hp1 HG02622.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-175-3033A>G | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112094008 | |||||||
| chr6:112094026 | A | G | 1 | a0001c0001t0001g0049 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.-175-3015A>G | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112094026 | |||||||
| chr6:112094045 | G | A | 1 | a0002c0002t0001g0019 | 4 | HG01884.hp2 HG02486.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.-175-2996G>A | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112094045 | |||||||
| chr6:112094148 | T | C | 18 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0013 others(15): Show |
110 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.-175-2893T>C | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112094148 | |||||||
| chr6:112094244 | G | C | 1 | a0001c0001t0019g0040 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-175-2797G>C | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112094244 | |||||||
| chr6:112094260 | C | G | 17 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0013 others(14): Show |
109 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.-175-2781C>G | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112094260 | |||||||
| chr6:112094361 | G | A | 6 | a0001c0001t0005g0011 a0001c0001t0005g0016 a0001c0001t0005g0059 others(3): Show |
18 | HG01891.hp2 HG02055.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.-175-2680G>A | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112094361 | |||||||
| chr6:112094364 | T | C | 1 | a0001c0001t0004g0042 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-175-2677T>C | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112094364 | |||||||
| chr6:112094446 | C | T | 1 | a0001c0001t0001g0030 | 2 | HG03942.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.-175-2595C>T | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112094446 | |||||||
| chr6:112094567 | A | G | 3 | a0001c0001t0007g0060 a0001c0001t0007g0061 a0001c0001t0007g0062 |
3 | HG01243.hp1 HG02622.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-175-2474A>G | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112094567 | |||||||
| chr6:112094817 | A | G | 24 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0013 others(21): Show |
128 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.-175-2224A>G | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112094817 | |||||||
| chr6:112094982 | A | G | 24 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0013 others(21): Show |
128 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.-175-2059A>G | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112094982 | |||||||
| chr6:112095043 | A | G | 1 | a0001c0001t0004g0039 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-175-1998A>G | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112095043 | |||||||
| chr6:112095114 | A | G | 25 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0013 others(22): Show |
130 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(127): Show |
intron_variant | MODIFIER | c.-175-1927A>G | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112095114 | |||||||
| chr6:112095281 | T | C | 1 | a0001c0001t0005g0059 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-175-1760T>C | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112095281 | |||||||
| chr6:112095426 | A | G | 1 | a0001c0001t0010g0025 | 2 | HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-175-1615A>G | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112095426 | |||||||
| chr6:112095461 | C | G | 42 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0013 others(39): Show |
201 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(198): Show |
intron_variant | MODIFIER | c.-175-1580C>G | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112095461 | |||||||
| chr6:112095634 | TCAAAAAA others(20): Show |
T | 1 | a0001c0001t0003g0052 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-175-1390_-175-136 others(31): Show |
FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr6 | 112095634 | ||||||
| chr6:112095635 | C | CA | 22 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(19): Show |
65 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.-175-1381dupA | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr6 | 112095635 | ||||||
| chr6:112095635 | CA | C | 7 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0003g0038 others(4): Show |
21 | HG00408.hp2 HG00673.hp1 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.-175-1381delA | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr6 | 112095635 | ||||||
| chr6:112095635 | CAA | C | 4 | a0001c0001t0005g0011 a0001c0001t0005g0059 a0001c0001t0019g0040 others(1): Show |
10 | HG02055.hp2 HG02109.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.-175-1382_-175-138 others(6): Show |
FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr6 | 112095635 | ||||||
| chr6:112095635 | CAAAAAA | C | 9 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0013 others(6): Show |
15 | HG01243.hp1 HG01981.hp2 HG02056.hp2 others(12): Show |
intron_variant | MODIFIER | c.-175-1386_-175-138 others(10): Show |
FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr6 | 112095635 | ||||||
| chr6:112095635 | CAAAAAAA | C | 8 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0013 others(5): Show |
85 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.-175-1387_-175-138 others(11): Show |
FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr6 | 112095635 | ||||||
| chr6:112095654 | A | C | 2 | a0001c0001t0002g0056 a0001c0001t0002g0063 |
2 | NA18965.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.-175-1387A>C | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112095654 | |||||||
| chr6:112095655 | A | C | 2 | a0001c0001t0002g0056 a0001c0001t0002g0063 |
2 | NA18965.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.-175-1386A>C | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112095655 | |||||||
| chr6:112095659 | A | C | 1 | a0001c0001t0004g0006 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-175-1382A>C | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112095659 | |||||||
| chr6:112095660 | A | C | 1 | a0001c0001t0002g0055 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-175-1381A>C | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112095660 | |||||||
| chr6:112095661 | C | A | 1 | a0003c0004t0016g0032 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-175-1380C>A | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112095661 | |||||||
| chr6:112095662 | C | A | 4 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0065 others(1): Show |
6 | HG01358.hp1 HG02738.hp1 NA18950.hp1 others(3): Show |
intron_variant | MODIFIER | c.-175-1379C>A | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112095662 | |||||||
| chr6:112095663 | A | C | 1 | a0003c0004t0016g0032 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-175-1378A>C | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112095663 | |||||||
| chr6:112095670 | AAAAAAAA others(1): Show |
A | 5 | a0001c0001t0005g0011 a0001c0001t0005g0016 a0001c0001t0005g0059 others(2): Show |
17 | HG01891.hp2 HG02055.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.-175-1363_-175-135 others(12): Show |
FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr6 | 112095670 | ||||||
| chr6:112095678 | G | A | 16 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0013 others(13): Show |
109 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.-175-1363G>A | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112095678 | |||||||
| chr6:112095679 | A | G | 16 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0013 others(13): Show |
109 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.-175-1362A>G | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112095679 | |||||||
| chr6:112095680 | A | G | 6 | a0001c0001t0005g0011 a0001c0001t0005g0016 a0001c0001t0005g0059 others(3): Show |
18 | HG01891.hp2 HG02055.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.-175-1361A>G | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112095680 | |||||||
| chr6:112095685 | A | G | 1 | a0001c0001t0002g0058 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.-175-1356A>G | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112095685 | |||||||
| chr6:112095752 | T | C | 1 | a0001c0001t0001g0033 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-175-1289T>C | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112095752 | |||||||
| chr6:112095844 | G | A | 7 | a0001c0001t0004g0006 a0001c0001t0004g0014 a0001c0001t0004g0018 others(4): Show |
36 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(33): Show |
intron_variant | MODIFIER | c.-175-1197G>A | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112095844 | |||||||
| chr6:112095993 | G | C | 1 | a0001c0001t0005g0016 | 5 | HG01891.hp2 HG02257.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.-175-1048G>C | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112095993 | |||||||
| chr6:112096150 | G | A | 38 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0013 others(35): Show |
196 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(193): Show |
intron_variant | MODIFIER | c.-175-891G>A | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112096150 | |||||||
| chr6:112096232 | G | A | 1 | a0001c0001t0014g0036 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-175-809G>A | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112096232 | |||||||
| chr6:112096283 | G | A | 6 | a0001c0001t0005g0011 a0001c0001t0005g0016 a0001c0001t0005g0059 others(3): Show |
18 | HG01891.hp2 HG02055.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.-175-758G>A | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112096283 | |||||||
| chr6:112096339 | G | A | 6 | a0001c0001t0005g0011 a0001c0001t0005g0016 a0001c0001t0005g0059 others(3): Show |
18 | HG01891.hp2 HG02055.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.-175-702G>A | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112096339 | |||||||
| chr6:112096377 | A | G | 18 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0013 others(15): Show |
110 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.-175-664A>G | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112096377 | |||||||
| chr6:112096433 | G | A | 1 | a0001c0001t0001g0028 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-175-608G>A | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112096433 | |||||||
| chr6:112096474 | T | TG | 18 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0013 others(15): Show |
110 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.-175-566dupG | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr6 | 112096474 | ||||||
| chr6:112096479 | A | G | 1 | a0001c0001t0006g0017 | 5 | HG02647.hp1 HG02895.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.-175-562A>G | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112096479 | |||||||
| chr6:112096521 | A | C | 1 | a0001c0001t0010g0025 | 2 | HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-175-520A>C | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112096521 | |||||||
| chr6:112096564 | C | A | 2 | a0001c0001t0003g0031 a0001c0001t0018g0031 |
2 | NA18939.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.-175-477C>A | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112096564 | |||||||
| chr6:112096687 | T | TAAAGAAT others(309): Show |
1 | a0001c0001t0002g0057 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-175-340_-175-339i others(318): Show |
FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr6 | 112096687 | ||||||
| chr6:112096777 | G | A | 1 | a0001c0001t0003g0052 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-175-264G>A | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112096777 | |||||||
| chr6:112096791 | A | T | 1 | a0001c0001t0010g0025 | 2 | HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-175-250A>T | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112096791 | |||||||
| chr6:112097020 | T | C | 6 | a0001c0001t0005g0011 a0001c0001t0005g0016 a0001c0001t0005g0059 others(3): Show |
18 | HG01891.hp2 HG02055.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.-175-21T>C | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112097020 | |||||||
| chr6:112097035 | C | T | 1 | a0001c0001t0001g0048 | 1 | NA19075.hp1 | splice_region_variant&intron_variant | LOW | c.-175-6C>T | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 1/3 | chr6 | 112097035 | |||||||
| chr6:112097257 | G | A | 1 | a0001c0001t0003g0009 | 9 | HG00099.hp1 HG01168.hp1 HG01175.hp1 others(6): Show |
intron_variant | MODIFIER | c.-15+56G>A | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 2/3 | chr6 | 112097257 | |||||||
| chr6:112097311 | G | A | 18 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0013 others(15): Show |
110 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.-15+110G>A | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 2/3 | chr6 | 112097311 | |||||||
| chr6:112097341 | C | T | 1 | a0001c0001t0019g0040 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-15+140C>T | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 2/3 | chr6 | 112097341 | |||||||
| chr6:112097439 | A | C | 1 | a0001c0001t0001g0020 | 3 | HG00621.hp1 NA18953.hp1 NA18961.hp2 |
intron_variant | MODIFIER | c.-15+238A>C | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 2/3 | chr6 | 112097439 | |||||||
| chr6:112097440 | T | C | 1 | a0001c0001t0001g0020 | 3 | HG00621.hp1 NA18953.hp1 NA18961.hp2 |
intron_variant | MODIFIER | c.-15+239T>C | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 2/3 | chr6 | 112097440 | |||||||
| chr6:112097482 | GTACTAAT others(16): Show |
G | 1 | a0001c0001t0001g0034 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-15+304_-15+326del others(23): Show |
FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 112097482 | ||||||
| chr6:112097520 | TACATTGT others(16): Show |
T | 1 | a0001c0001t0003g0038 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-15+360_-15+382del others(23): Show |
FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 112097520 | ||||||
| chr6:112097570 | T | TTGTGTAC others(16): Show |
1 | a0001c0001t0010g0025 | 2 | HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-15+391_-15+392ins others(23): Show |
FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr6 | 112097570 | ||||||
| chr6:112097593 | T | C | 1 | a0001c0001t0010g0025 | 2 | HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-15+392T>C | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 2/3 | chr6 | 112097593 | |||||||
| chr6:112097620 | G | A | 1 | a0001c0001t0007g0060 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-15+419G>A | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 2/3 | chr6 | 112097620 | |||||||
| chr6:112097660 | CAG | C | 16 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0013 others(13): Show |
104 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.-15+460_-15+461del others(2): Show |
FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 2/3 | chr6 | 112097660 | |||||||
| chr6:112097671 | A | G | 1 | a0001c0001t0010g0025 | 2 | HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-15+470A>G | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 2/3 | chr6 | 112097671 | |||||||
| chr6:112097686 | T | G | 1 | a0001c0001t0002g0022 | 3 | HG01109.hp2 HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.-15+485T>G | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 2/3 | chr6 | 112097686 | |||||||
| chr6:112097776 | A | G | 1 | a0001c0001t0001g0047 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-15+575A>G | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 2/3 | chr6 | 112097776 | |||||||
| chr6:112097863 | C | T | 1 | a0001c0001t0001g0046 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-15+662C>T | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 2/3 | chr6 | 112097863 | |||||||
| chr6:112097960 | A | T | 1 | a0001c0001t0003g0038 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-15+759A>T | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 2/3 | chr6 | 112097960 | |||||||
| chr6:112098050 | G | A | 6 | a0001c0001t0002g0004 a0001c0001t0002g0013 a0001c0001t0002g0055 others(3): Show |
46 | HG00544.hp2 HG00558.hp2 HG00673.hp2 others(43): Show |
intron_variant | MODIFIER | c.-15+849G>A | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 2/3 | chr6 | 112098050 | |||||||
| chr6:112098203 | G | A | 6 | a0001c0001t0005g0011 a0001c0001t0005g0016 a0001c0001t0005g0059 others(3): Show |
18 | HG01891.hp2 HG02055.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.-15+1002G>A | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 2/3 | chr6 | 112098203 | |||||||
| chr6:112098268 | C | T | 1 | a0001c0001t0006g0017 | 5 | HG02647.hp1 HG02895.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.-14-1002C>T | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 2/3 | chr6 | 112098268 | |||||||
| chr6:112098274 | C | A | 1 | a0001c0001t0003g0053 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-14-996C>A | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 2/3 | chr6 | 112098274 | |||||||
| chr6:112098306 | T | A | 25 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0013 others(22): Show |
130 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(127): Show |
intron_variant | MODIFIER | c.-14-964T>A | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 2/3 | chr6 | 112098306 | |||||||
| chr6:112098399 | A | G | 1 | a0001c0001t0004g0044 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-14-871A>G | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 2/3 | chr6 | 112098399 | |||||||
| chr6:112098461 | C | T | 16 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0013 others(13): Show |
104 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.-14-809C>T | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 2/3 | chr6 | 112098461 | |||||||
| chr6:112098502 | A | T | 1 | a0001c0001t0002g0013 | 7 | HG02074.hp2 NA18960.hp1 NA18968.hp1 others(4): Show |
intron_variant | MODIFIER | c.-14-768A>T | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 2/3 | chr6 | 112098502 | |||||||
| chr6:112098607 | C | T | 1 | a0001c0001t0006g0017 | 5 | HG02647.hp1 HG02895.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.-14-663C>T | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 2/3 | chr6 | 112098607 | |||||||
| chr6:112098801 | C | T | 1 | a0001c0001t0001g0029 | 2 | HG01071.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.-14-469C>T | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 2/3 | chr6 | 112098801 | |||||||
| chr6:112098849 | G | A | 24 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0013 others(21): Show |
128 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.-14-421G>A | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 2/3 | chr6 | 112098849 | |||||||
| chr6:112098927 | A | G | 1 | a0001c0001t0007g0061 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-14-343A>G | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 2/3 | chr6 | 112098927 | |||||||
| chr6:112099024 | T | C | 12 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0013 others(9): Show |
98 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.-14-246T>C | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 2/3 | chr6 | 112099024 | |||||||
| chr6:112099053 | G | A | 1 | a0001c0001t0003g0052 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-14-217G>A | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 2/3 | chr6 | 112099053 | |||||||
| chr6:112099086 | G | T | 1 | a0001c0001t0014g0036 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-14-184G>T | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 2/3 | chr6 | 112099086 | |||||||
| chr6:112099183 | A | G | 1 | a0001c0001t0001g0015 | 5 | HG01168.hp2 HG01169.hp1 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.-14-87A>G | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 2/3 | chr6 | 112099183 | |||||||
| chr6:112099241 | G | A | 3 | a0001c0001t0005g0011 a0001c0001t0005g0016 a0001c0001t0005g0059 |
14 | HG01891.hp2 HG02257.hp2 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.-14-29G>A | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 2/3 | chr6 | 112099241 | |||||||
| chr6:112099482 | T | G | 24 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0013 others(21): Show |
128 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.125+74T>G | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 3/3 | chr6 | 112099482 | |||||||
| chr6:112099500 | T | C | 24 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0013 others(21): Show |
128 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.125+92T>C | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 3/3 | chr6 | 112099500 | |||||||
| chr6:112099812 | C | A | 6 | a0001c0001t0005g0011 a0001c0001t0005g0016 a0001c0001t0005g0059 others(3): Show |
18 | HG01891.hp2 HG02055.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.125+404C>A | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 3/3 | chr6 | 112099812 | |||||||
| chr6:112099855 | G | A | 1 | a0001c0001t0014g0036 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.125+447G>A | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 3/3 | chr6 | 112099855 | |||||||
| chr6:112100102 | C | T | 18 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0013 others(15): Show |
110 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.126-568C>T | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 3/3 | chr6 | 112100102 | |||||||
| chr6:112100117 | C | T | 42 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0013 others(39): Show |
201 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(198): Show |
intron_variant | MODIFIER | c.126-553C>T | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 3/3 | chr6 | 112100117 | |||||||
| chr6:112100518 | C | T | 18 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0013 others(15): Show |
110 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.126-152C>T | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 3/3 | chr6 | 112100518 | |||||||
| chr6:112100519 | G | A | 1 | a0001c0001t0001g0045 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.126-151G>A | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 3/3 | chr6 | 112100519 | |||||||
| chr6:112100602 | T | C | 5 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0051 others(2): Show |
31 | HG00140.hp1 HG00280.hp2 HG00597.hp1 others(28): Show |
intron_variant | MODIFIER | c.126-68T>C | FAM229B | ENSG00000203778.8 | transcript | ENST00000368656.7 | protein_coding | 3/3 | chr6 | 112100602 |