Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 55274 |
| ensemblid | ENSG00000130024.15 |
| hgncid | 18250 |
| symbol | PHF10 |
| name | PHD finger protein 10 |
| refseq_nuc | NM_018288.4 |
| refseq_prot | NP_060758.2 |
| ensembl_nuc | ENST00000339209.9 |
| ensembl_prot | ENSP00000341805.4 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 169703902 |
| end | 169724500 |
| strand | - |
| ver | v1.2 |
| region | chr6:169703902-169724500 |
| region5000 | chr6:169698902-169729500 |
| regionname0 | PHF10_chr6_169703902_169724500 |
| regionname5000 | PHF10_chr6_169698902_169729500 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 498 | 391 | 95 | 65 | 183 | 10 | 36 | 145 | PHF10_chr6_169698902_169729500 | PHF10 | MAAAA others(493): Show |
chr6 | 169698902 | 169729500 |
| a0002 | 0/0 | 498 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | MAAAA others(493): Show |
chr6 | 169698902 | 169729500 |
| a0003 | 0/0 | 498 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | MAAAA others(493): Show |
chr6 | 169698902 | 169729500 |
| a0004 | 0/0 | 259 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PHF10_chr6_169698902_169729500 | PHF10 | MAAAA others(254): Show |
chr6 | 169698902 | 169729500 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1494 | 363 | 90 | 63 | 171 | 10 | 27 | PHF10_chr6_169698902_169729500 | PHF10 | ATGGC others(1489): Show |
chr6 | 169698902 | 169729500 | ||
| a0001c0002 | 0/0 | 1494 | 27 | 4 | 2 | 12 | 0 | 9 | PHF10_chr6_169698902_169729500 | PHF10 | ATGGC others(1489): Show |
chr6 | 169698902 | 169729500 | ||
| a0001c0006 | 0/0 | 1494 | 1 | 1 | 0 | 0 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | ATGGC others(1489): Show |
chr6 | 169698902 | 169729500 | ||
| a0002c0005 | 0/0 | 1494 | 1 | 0 | 1 | 0 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | ATGGC others(1489): Show |
chr6 | 169698902 | 169729500 | ||
| a0003c0003 | 0/0 | 1494 | 1 | 1 | 0 | 0 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | ATGGC others(1489): Show |
chr6 | 169698902 | 169729500 | ||
| a0004c0004 | 0/0 | 1563 | 1 | 0 | 0 | 1 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | ATGGC others(1558): Show |
chr6 | 169698902 | 169729500 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2189 | 154 | 20 | 29 | 96 | 2 | 7 | PHF10_chr6_169698902_169729500 | PHF10 | GAGTA others(2184): Show |
chr6 | 169698902 | 169729500 |
| a0001c0001t0002 | 1/0 | 2167 | 78 | 35 | 15 | 8 | 5 | 14 | PHF10_chr6_169698902_169729500 | PHF10 | GAGTA others(2162): Show |
chr6 | 169698902 | 169729500 |
| a0001c0001t0003 | 0/1 | 2189 | 101 | 19 | 13 | 59 | 3 | 6 | PHF10_chr6_169698902_169729500 | PHF10 | GAGTA others(2184): Show |
chr6 | 169698902 | 169729500 |
| a0001c0001t0004 | 0/0 | 2149 | 12 | 3 | 1 | 8 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | GAGTA others(2144): Show |
chr6 | 169698902 | 169729500 |
| a0001c0001t0005 | 0/0 | 2167 | 3 | 3 | 0 | 0 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | GAGTA others(2162): Show |
chr6 | 169698902 | 169729500 |
| a0001c0001t0006 | 0/0 | 2170 | 3 | 3 | 0 | 0 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | GAGTA others(2165): Show |
chr6 | 169698902 | 169729500 |
| a0001c0001t0007 | 0/0 | 2211 | 2 | 0 | 2 | 0 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | GAGTA others(2206): Show |
chr6 | 169698902 | 169729500 |
| a0001c0001t0008 | 0/0 | 2211 | 1 | 1 | 0 | 0 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | GAGTA others(2206): Show |
chr6 | 169698902 | 169729500 |
| a0001c0001t0009 | 0/0 | 2192 | 1 | 0 | 1 | 0 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | GAGTA others(2187): Show |
chr6 | 169698902 | 169729500 |
| a0001c0001t0010 | 0/0 | 2189 | 1 | 1 | 0 | 0 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | GAGTA others(2184): Show |
chr6 | 169698902 | 169729500 |
| a0001c0001t0011 | 0/0 | 2189 | 1 | 1 | 0 | 0 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | GAGTA others(2184): Show |
chr6 | 169698902 | 169729500 |
| a0001c0001t0012 | 0/0 | 2167 | 1 | 0 | 1 | 0 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | GAGTA others(2162): Show |
chr6 | 169698902 | 169729500 |
| a0001c0001t0013 | 0/0 | 2167 | 1 | 1 | 0 | 0 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | GAGTA others(2162): Show |
chr6 | 169698902 | 169729500 |
| a0001c0001t0014 | 0/0 | 2167 | 1 | 0 | 1 | 0 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | GAGTA others(2162): Show |
chr6 | 169698902 | 169729500 |
| a0001c0001t0015 | 0/0 | 2152 | 1 | 1 | 0 | 0 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | GAGTA others(2147): Show |
chr6 | 169698902 | 169729500 |
| a0001c0001t0016 | 0/0 | 2189 | 1 | 1 | 0 | 0 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | GAGTA others(2184): Show |
chr6 | 169698902 | 169729500 |
| a0001c0001t0017 | 0/0 | 2150 | 1 | 1 | 0 | 0 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | GAGTA others(2145): Show |
chr6 | 169698902 | 169729500 |
| a0001c0002t0002 | 0/0 | 2167 | 27 | 4 | 2 | 12 | 0 | 9 | PHF10_chr6_169698902_169729500 | PHF10 | GAGTA others(2162): Show |
chr6 | 169698902 | 169729500 |
| a0001c0006t0001 | 0/0 | 2189 | 1 | 1 | 0 | 0 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | GAGTA others(2184): Show |
chr6 | 169698902 | 169729500 |
| a0002c0005t0002 | 0/0 | 2167 | 1 | 0 | 1 | 0 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | GAGTA others(2162): Show |
chr6 | 169698902 | 169729500 |
| a0003c0003t0003 | 0/0 | 2189 | 1 | 1 | 0 | 0 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | GAGTA others(2184): Show |
chr6 | 169698902 | 169729500 |
| a0004c0004t0003 | 0/0 | 2258 | 1 | 0 | 0 | 1 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | GAGTA others(2253): Show |
chr6 | 169698902 | 169729500 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 39 | 1 | 6 | 32 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0001t0001g0002 | 0/0 | 32 | 0 | 7 | 21 | 0 | 4 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0001t0001g0007 | 0/0 | 8 | 0 | 3 | 5 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0001t0001g0010 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0001t0001g0013 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0001t0001g0014 | 0/0 | 5 | 1 | 3 | 0 | 1 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0001t0001g0015 | 0/0 | 5 | 0 | 3 | 0 | 1 | 1 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0001t0001g0024 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0001t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0001t0001g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0001t0001g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0001t0002g0004 | 0/0 | 18 | 1 | 5 | 3 | 0 | 9 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0001t0002g0011 | 1/0 | 6 | 1 | 2 | 0 | 2 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0001t0002g0017 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0001t0002g0018 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0001t0002g0019 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0001t0002g0021 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0001t0002g0022 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0001t0002g0023 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0001t0002g0027 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0001t0002g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0001t0002g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0001t0002g0048 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0001t0002g0049 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0001t0002g0050 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0001t0002g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0001t0002g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0001t0002g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0001t0002g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0001t0003g0003 | 0/0 | 19 | 0 | 0 | 16 | 1 | 2 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0001t0003g0005 | 0/0 | 17 | 0 | 1 | 14 | 1 | 1 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0001t0003g0006 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0001t0003g0016 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0001t0003g0020 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0001t0003g0025 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0001t0003g0026 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0001t0003g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0001t0003g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0001t0003g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0001t0003g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0001t0003g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0001t0003g0041 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0001t0003g0042 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0001t0003g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0001t0003g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0001t0003g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0001t0003g0099 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0001t0003g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0001t0003g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0001t0003g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0001t0003g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0001t0003g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0001t0003g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0001t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0001t0003g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0001t0003g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0001t0003g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0001t0003g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0001t0003g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0001t0003g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0001t0003g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0001t0003g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0001t0003g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0001t0003g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0001t0003g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0001t0003g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0001t0003g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0001t0003g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0001t0003g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0001t0004g0009 | 0/0 | 7 | 1 | 0 | 6 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0001t0004g0028 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0001t0004g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0001t0004g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0001t0005g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0001t0005g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0001t0006g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0001t0006g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0001t0006g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0001t0007g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0001t0008g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0001t0009g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0001t0010g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0001t0011g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0001t0012g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0001t0013g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0001t0014g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0001t0015g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0001t0016g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0001t0017g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0002t0002g0008 | 0/0 | 7 | 0 | 1 | 0 | 0 | 6 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0002t0002g0012 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0002t0002g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0002t0002g0051 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0002t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0002t0002g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0002t0002g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0002t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0002t0002g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0002t0002g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0002t0002g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0002t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0002t0002g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0002t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0001c0006t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0002c0005t0002g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0003c0003t0003g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| a0004c0004t0003g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0003 | g0003 | EUR | GBR | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0136 | EUR | GBR | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG00408 | hp2 | a0001 | c0001 | t0003 | g0106 | EAS | CHS | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG00438 | hp1 | a0001 | c0001 | t0004 | g0009 | EAS | CHS | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG00438 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | CHS | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | CHS | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG00558 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | CHS | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG00597 | hp2 | a0001 | c0001 | t0004 | g0009 | EAS | CHS | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG00609 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | CHS | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG00621 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | CHS | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG00639 | hp1 | a0001 | c0002 | t0002 | g0008 | AMR | PUR | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0140 | AMR | PUR | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | CHS | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG00735 | hp1 | a0001 | c0001 | t0003 | g0016 | AMR | PUR | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0064 | AMR | PUR | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0050 | AMR | PUR | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG00738 | hp2 | a0001 | c0001 | t0003 | g0042 | AMR | PUR | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG01069 | hp1 | a0001 | c0001 | t0004 | g0028 | AMR | PUR | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG01069 | hp2 | a0001 | c0001 | t0007 | g0029 | AMR | PUR | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG01071 | hp1 | a0001 | c0001 | t0007 | g0029 | AMR | PUR | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG01074 | hp1 | a0001 | c0001 | t0003 | g0041 | AMR | PUR | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0141 | AMR | PUR | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG01081 | hp1 | a0001 | c0001 | t0003 | g0005 | AMR | PUR | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0050 | AMR | PUR | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG01099 | hp1 | a0001 | c0001 | t0003 | g0026 | AMR | PUR | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG01099 | hp2 | a0001 | c0001 | t0003 | g0118 | AMR | PUR | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0011 | AMR | PUR | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0018 | AMR | PUR | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG01168 | hp2 | a0001 | c0001 | t0014 | g0154 | AMR | PUR | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0078 | AMR | PUR | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0011 | AMR | PUR | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0130 | AMR | PUR | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG01258 | hp1 | a0001 | c0001 | t0012 | g0127 | AMR | CLM | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG01346 | hp2 | a0002 | c0005 | t0002 | g0134 | AMR | CLM | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG01433 | hp1 | a0001 | c0001 | t0003 | g0112 | AMR | CLM | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG01433 | hp2 | a0001 | c0001 | t0009 | g0093 | AMR | CLM | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0149 | EUR | IBS | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0011 | EUR | IBS | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0011 | EUR | IBS | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0014 | EUR | IBS | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0027 | AFR | ACB | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | ACB | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG01891 | hp1 | a0001 | c0001 | t0005 | g0044 | AFR | ACB | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG01891 | hp2 | a0003 | c0003 | t0003 | g0095 | AFR | ACB | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG01934 | hp2 | a0001 | c0002 | t0002 | g0145 | AMR | PEL | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | PEL | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG01975 | hp1 | a0001 | c0001 | t0003 | g0119 | AMR | PEL | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | PEL | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0135 | AMR | PEL | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG01981 | hp2 | a0001 | c0001 | t0003 | g0020 | AMR | PEL | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG01993 | hp2 | a0001 | c0001 | t0003 | g0020 | AMR | PEL | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG02004 | hp1 | a0001 | c0001 | t0003 | g0103 | AMR | PEL | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0058 | AMR | PEL | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | KHV | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG02027 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | KHV | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0137 | EAS | KHV | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | ACB | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG02055 | hp2 | a0001 | c0001 | t0003 | g0108 | AFR | ACB | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG02056 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | KHV | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG02071 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | KHV | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | KHV | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | KHV | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG02080 | hp2 | a0001 | c0002 | t0002 | g0150 | EAS | KHV | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | KHV | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG02132 | hp2 | a0001 | c0001 | t0003 | g0025 | EAS | KHV | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | ACB | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0027 | AFR | ACB | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG02165 | hp2 | a0001 | c0001 | t0003 | g0101 | EAS | CDX | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG02257 | hp1 | a0001 | c0001 | t0003 | g0041 | AFR | ACB | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0152 | AFR | ACB | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0018 | AFR | ACB | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG02258 | hp2 | a0001 | c0001 | t0006 | g0125 | AFR | ACB | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG02273 | hp2 | a0001 | c0001 | t0003 | g0020 | AMR | PEL | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG02280 | hp1 | a0001 | c0001 | t0004 | g0028 | AFR | ACB | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0017 | AFR | ACB | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG02293 | hp2 | a0001 | c0001 | t0003 | g0042 | AMR | PEL | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0131 | AMR | PEL | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0017 | AFR | ACB | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG02451 | hp2 | a0001 | c0001 | t0005 | g0044 | AFR | ACB | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0019 | AFR | GWD | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG02572 | hp2 | a0001 | c0001 | t0003 | g0037 | AFR | GWD | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG02602 | hp2 | a0001 | c0002 | t0002 | g0008 | SAS | PJL | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG02615 | hp1 | a0001 | c0001 | t0004 | g0028 | AFR | GWD | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG02615 | hp2 | a0001 | c0002 | t0002 | g0143 | AFR | GWD | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0151 | AFR | GWD | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG02622 | hp2 | a0001 | c0002 | t0002 | g0051 | AFR | GWD | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0022 | AFR | GWD | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG02630 | hp2 | a0001 | c0001 | t0017 | g0159 | AFR | GWD | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | GWD | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG02647 | hp2 | a0001 | c0001 | t0003 | g0016 | AFR | GWD | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG02683 | hp1 | a0001 | c0002 | t0002 | g0144 | SAS | PJL | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG02683 | hp2 | a0001 | c0002 | t0002 | g0008 | SAS | PJL | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0017 | AFR | GWD | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG02717 | hp2 | a0001 | c0001 | t0003 | g0016 | AFR | GWD | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0023 | AFR | GWD | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0022 | AFR | GWD | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0004 | SAS | PJL | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG02738 | hp1 | a0001 | c0002 | t0002 | g0008 | SAS | PJL | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0004 | SAS | PJL | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG02809 | hp1 | a0001 | c0001 | t0016 | g0158 | AFR | GWD | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0022 | AFR | GWD | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0018 | AFR | GWD | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0023 | AFR | GWD | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG02886 | hp2 | a0001 | c0001 | t0006 | g0124 | AFR | GWD | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | GWD | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG02895 | hp2 | a0001 | c0002 | t0002 | g0051 | AFR | GWD | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG02896 | hp1 | a0001 | c0001 | t0003 | g0043 | AFR | GWD | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0129 | AFR | GWD | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG02897 | hp1 | a0001 | c0002 | t0002 | g0148 | AFR | GWD | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG02897 | hp2 | a0001 | c0001 | t0003 | g0043 | AFR | GWD | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | ESN | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0019 | AFR | ESN | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG02965 | hp1 | a0001 | c0001 | t0003 | g0121 | AFR | ESN | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG02965 | hp2 | a0001 | c0001 | t0006 | g0126 | AFR | ESN | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG02970 | hp2 | a0001 | c0001 | t0003 | g0040 | AFR | ESN | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG02976 | hp1 | a0001 | c0001 | t0003 | g0016 | AFR | ESN | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0046 | AFR | ESN | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0022 | AFR | GWD | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | GWD | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG03098 | hp1 | a0001 | c0001 | t0008 | g0052 | AFR | MSL | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG03098 | hp2 | a0001 | c0006 | t0001 | g0077 | AFR | MSL | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0019 | AFR | ESN | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG03139 | hp2 | a0001 | c0001 | t0013 | g0153 | AFR | ESN | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0019 | AFR | ESN | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0018 | AFR | ESN | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | MSL | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0046 | AFR | MSL | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0011 | AFR | MSL | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG03225 | hp2 | a0001 | c0001 | t0010 | g0094 | AFR | MSL | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0023 | AFR | MSL | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG03453 | hp2 | a0001 | c0001 | t0003 | g0037 | AFR | MSL | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0047 | AFR | MSL | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG03486 | hp2 | a0001 | c0001 | t0003 | g0109 | AFR | MSL | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG03491 | hp1 | a0001 | c0001 | t0003 | g0098 | SAS | PJL | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0049 | SAS | PJL | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0048 | SAS | PJL | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0049 | SAS | PJL | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | ESN | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG03516 | hp2 | a0001 | c0001 | t0003 | g0026 | AFR | ESN | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG03540 | hp1 | a0001 | c0001 | t0004 | g0009 | AFR | GWD | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0017 | AFR | GWD | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG03579 | hp1 | a0001 | c0001 | t0003 | g0117 | AFR | MSL | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | MSL | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0004 | SAS | PJL | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0004 | SAS | STU | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG03688 | hp2 | a0001 | c0001 | t0003 | g0114 | SAS | STU | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0004 | SAS | PJL | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0085 | SAS | PJL | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0004 | SAS | PJL | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG03710 | hp2 | a0001 | c0002 | t0002 | g0138 | SAS | PJL | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0133 | SAS | BEB | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG03834 | hp2 | a0001 | c0001 | t0003 | g0105 | SAS | BEB | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG03927 | hp1 | a0001 | c0001 | t0003 | g0003 | SAS | BEB | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0004 | SAS | BEB | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0004 | SAS | BEB | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG04115 | hp1 | a0001 | c0001 | t0003 | g0003 | SAS | STU | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG04115 | hp2 | a0001 | c0002 | t0002 | g0008 | SAS | STU | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0048 | SAS | BEB | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG04184 | hp2 | a0001 | c0001 | t0003 | g0005 | SAS | BEB | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG04199 | hp1 | a0001 | c0002 | t0002 | g0008 | SAS | STU | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | STU | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0086 | SAS | STU | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG04204 | hp2 | a0001 | c0002 | t0002 | g0008 | SAS | STU | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0004 | SAS | STU | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG04228 | hp2 | a0001 | c0002 | t0002 | g0139 | SAS | STU | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | YRI | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0027 | AFR | YRI | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | YRI | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | YRI | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA18942 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA18944 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA18944 | hp2 | a0001 | c0001 | t0003 | g0038 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA18945 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA18945 | hp2 | a0001 | c0001 | t0004 | g0155 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA18947 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA18948 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA18949 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA18951 | hp1 | a0001 | c0001 | t0004 | g0009 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA18953 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA18954 | hp1 | a0001 | c0001 | t0004 | g0009 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA18954 | hp2 | a0001 | c0002 | t0002 | g0146 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA18957 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA18959 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA18961 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA18961 | hp2 | a0001 | c0002 | t0002 | g0012 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA18963 | hp1 | a0001 | c0002 | t0002 | g0142 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA18965 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA18966 | hp1 | a0001 | c0002 | t0002 | g0012 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA18970 | hp2 | a0001 | c0001 | t0003 | g0036 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA18973 | hp1 | a0001 | c0001 | t0003 | g0111 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA18973 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA18974 | hp1 | a0001 | c0001 | t0004 | g0009 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA18978 | hp1 | a0001 | c0001 | t0003 | g0039 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA18979 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA18981 | hp1 | a0001 | c0001 | t0003 | g0102 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA18981 | hp2 | a0001 | c0002 | t0002 | g0045 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA18986 | hp2 | a0001 | c0002 | t0002 | g0012 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA18987 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA18989 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA18989 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA18990 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA18993 | hp1 | a0001 | c0001 | t0003 | g0113 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA18995 | hp1 | a0001 | c0002 | t0002 | g0045 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA18995 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA18998 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA18998 | hp2 | a0001 | c0001 | t0003 | g0020 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA18999 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA19001 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA19003 | hp1 | a0001 | c0001 | t0003 | g0038 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA19005 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA19012 | hp2 | a0004 | c0004 | t0003 | g0097 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA19030 | hp1 | a0001 | c0001 | t0005 | g0123 | AFR | LWK | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0019 | AFR | LWK | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0018 | AFR | LWK | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | LWK | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA19054 | hp1 | a0001 | c0002 | t0002 | g0012 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA19055 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA19056 | hp1 | a0001 | c0001 | t0003 | g0036 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA19057 | hp1 | a0001 | c0002 | t0002 | g0128 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA19058 | hp1 | a0001 | c0001 | t0003 | g0104 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA19060 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA19062 | hp2 | a0001 | c0001 | t0004 | g0156 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA19065 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA19066 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA19067 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA19068 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA19070 | hp1 | a0001 | c0001 | t0003 | g0116 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA19076 | hp1 | a0001 | c0001 | t0003 | g0110 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA19077 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA19077 | hp2 | a0001 | c0001 | t0003 | g0039 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA19078 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA19079 | hp1 | a0001 | c0001 | t0003 | g0120 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA19080 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA19084 | hp1 | a0001 | c0001 | t0004 | g0009 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA19084 | hp2 | a0001 | c0002 | t0002 | g0012 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA19085 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA19086 | hp2 | a0001 | c0001 | t0003 | g0025 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA19087 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA19088 | hp1 | a0001 | c0001 | t0003 | g0115 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA19090 | hp1 | a0001 | c0002 | t0002 | g0012 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA19090 | hp2 | a0001 | c0001 | t0003 | g0025 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA19240 | hp1 | a0001 | c0001 | t0011 | g0122 | AFR | YRI | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0147 | AFR | YRI | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | ASW | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0023 | AFR | ASW | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA20752 | hp1 | a0001 | c0001 | t0003 | g0100 | EUR | TSI | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0015 | EUR | TSI | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA20805 | hp1 | a0001 | c0001 | t0003 | g0005 | EUR | TSI | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0132 | EUR | TSI | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG02109 | hp1 | a0001 | c0001 | t0003 | g0096 | AFR | ACB | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG02486 | hp2 | a0001 | c0001 | t0003 | g0107 | AFR | ACB | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG02559 | hp1 | a0001 | c0001 | t0015 | g0157 | AFR | ACB | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG02559 | hp2 | a0001 | c0001 | t0003 | g0016 | AFR | ACB | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | MSL | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0017 | AFR | MSL | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG06807 | hp1 | a0001 | c0001 | t0003 | g0040 | AFR | USA | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| HG06807 | hp2 | a0001 | c0001 | t0003 | g0026 | AFR | USA | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0047 | AFR | USA | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | USA | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0003 | g0099 | REF | REF | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0011 | REF | REF | PHF10_chr6_169698902_169729500 | PHF10 | chr6 | 169698902 | 169729500 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:169705217 | G | A | 1 | a0002 | 1 | HG01346.hp2 | missense_variant | MODERATE | c.1327C>T | p.His443Tyr | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 11/12 | 1896/2167 | 1327/1497 | 443/498 | chr6 | 169705217 | |||
| chr6:169714760 | G | GGATGGGG others(62): Show |
1 | a0004 | 1 | NA19012.hp2 | stop_gained&conservative_inframe_insertion | HIGH | c.775_776insATTAGACC others(61): Show |
p.Ile258_Pro259insHi others(67): Show |
PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 7/12 | 1344/2167 | 775/1497 | 259/498 | chr6 | 169714760 | |||
| chr6:169714766 | A | T | 1 | a0004 | 1 | NA19012.hp2 | missense_variant | MODERATE | c.770T>A | p.Leu257His | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 7/12 | 1339/2167 | 770/1497 | 257/498 | chr6 | 169714766 | |||
| chr6:169723861 | C | T | 1 | a0003 | 1 | HG01891.hp2 | missense_variant | MODERATE | c.71G>A | p.Gly24Glu | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 1/12 | 640/2167 | 71/1497 | 24/498 | chr6 | 169723861 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:169705629 | T | C | 1 | a0001c0006 | 1 | HG03098.hp2 | synonymous_variant | LOW | c.1209A>G | p.Gln403Gln | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 10/12 | 1778/2167 | 1209/1497 | 403/498 | chr6 | 169705629 | |||
| chr6:169710308 | T | C | 1 | a0001c0002 | 27 | HG00639.hp1 HG01934.hp2 HG02080.hp2 others(24): Show |
synonymous_variant | LOW | c.1041A>G | p.Lys347Lys | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 9/12 | 1610/2167 | 1041/1497 | 347/498 | chr6 | 169710308 | |||
| chr6:169714765 | G | C | 1 | a0004c0004 | 1 | NA19012.hp2 | synonymous_variant | LOW | c.771C>G | p.Leu257Leu | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 7/12 | 1340/2167 | 771/1497 | 257/498 | chr6 | 169714765 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:169723934 | G | A | 2 | a0001c0001t0004 a0001c0001t0015 |
13 | HG00438.hp1 HG00597.hp2 HG01069.hp1 others(10): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-3C>T | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 1/12 | chr6 | 169723934 | |||||||
| chr6:169723998 | T | C | 2 | a0001c0001t0008 a0001c0001t0011 |
2 | HG03098.hp1 NA19240.hp1 |
5_prime_UTR_variant | MODIFIER | c.-67A>G | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 1/12 | 67 | chr6 | 169723998 | ||||||
| chr6:169723998 | T | TGCC | 3 | a0001c0001t0006 a0001c0001t0009 a0001c0001t0015 |
5 | HG01433.hp2 HG02258.hp2 HG02559.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-70_-68dupGGC | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 1/12 | 68 | chr6 | 169723998 | ||||||
| chr6:169724026 | C | A | 1 | a0001c0001t0013 | 1 | HG03139.hp2 | 5_prime_UTR_variant | MODIFIER | c.-95G>T | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 1/12 | 95 | chr6 | 169724026 | ||||||
| chr6:169724030 | C | A | 1 | a0001c0001t0014 | 1 | HG01168.hp2 | 5_prime_UTR_variant | MODIFIER | c.-99G>T | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 1/12 | 99 | chr6 | 169724030 | ||||||
| chr6:169724115 | C | T | 1 | a0001c0001t0012 | 1 | HG01258.hp1 | 5_prime_UTR_variant | MODIFIER | c.-184G>A | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 1/12 | 184 | chr6 | 169724115 | ||||||
| chr6:169724161 | G | A | 1 | a0001c0001t0010 | 1 | HG03225.hp2 | 5_prime_UTR_variant | MODIFIER | c.-230C>T | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 1/12 | 230 | chr6 | 169724161 | ||||||
| chr6:169724317 | A | G | 7 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0006 others(4): Show |
164 | HG00408.hp1 HG00544.hp1 HG00544.hp2 others(161): Show |
5_prime_UTR_variant | MODIFIER | c.-386T>C | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 1/12 | 386 | chr6 | 169724317 | ||||||
| chr6:169724323 | T | TTCAGCCC others(15): Show |
1 | a0001c0001t0016 | 1 | HG02809.hp1 | 5_prime_UTR_variant | MODIFIER | c.-393_-392insGGCGAG others(16): Show |
PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 1/12 | 393 | chr6 | 169724323 | ||||||
| chr6:169724335 | A | ACTCGCTC others(15): Show |
8 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0009 others(5): Show |
260 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(257): Show |
5_prime_UTR_variant | MODIFIER | c.-426_-405dupCGGCGG others(16): Show |
PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 1/12 | 405 | chr6 | 169724335 | ||||||
| chr6:169724335 | A | ACTCGCTC others(37): Show |
2 | a0001c0001t0007 a0001c0001t0008 |
3 | HG01069.hp2 HG01071.hp1 HG03098.hp1 |
5_prime_UTR_variant | MODIFIER | c.-405_-404insCGGCGG others(38): Show |
PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 1/12 | 405 | chr6 | 169724335 | ||||||
| chr6:169724335 | A | G | 1 | a0001c0001t0016 | 1 | HG02809.hp1 | 5_prime_UTR_variant | MODIFIER | c.-404T>C | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 1/12 | 404 | chr6 | 169724335 | ||||||
| chr6:169724380 | CCGCCTCA others(11): Show |
C | 2 | a0001c0001t0004 a0001c0001t0015 |
13 | HG00438.hp1 HG00597.hp2 HG01069.hp1 others(10): Show |
5_prime_UTR_variant | MODIFIER | c.-467_-450delAGCGGC others(12): Show |
PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 1/12 | 450 | chr6 | 169724380 | ||||||
| chr6:169724393 | G | C | 1 | a0001c0001t0008 | 1 | HG03098.hp1 | 5_prime_UTR_variant | MODIFIER | c.-462C>G | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 1/12 | 462 | chr6 | 169724393 | ||||||
| chr6:169724418 | G | C | 1 | a0001c0001t0016 | 1 | HG02809.hp1 | 5_prime_UTR_variant | MODIFIER | c.-487C>G | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 1/12 | 487 | chr6 | 169724418 | ||||||
| chr6:169724436 | CCCTCAGC others(10): Show |
C | 1 | a0001c0001t0017 | 1 | HG02630.hp2 | 5_prime_UTR_variant | MODIFIER | c.-522_-506delCGGCCG others(11): Show |
PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 1/12 | 506 | chr6 | 169724436 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:169704178 | C | G | 7 | a0001c0002t0002g0012 a0001c0002t0002g0045 a0001c0002t0002g0128 others(4): Show |
13 | HG02080.hp2 HG03710.hp2 NA18954.hp2 others(10): Show |
intron_variant | MODIFIER | c.1412-90G>C | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 11/11 | chr6 | 169704178 | |||||||
| chr6:169704347 | G | C | 1 | a0001c0001t0003g0108 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1412-259C>G | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 11/11 | chr6 | 169704347 | |||||||
| chr6:169704394 | A | G | 2 | a0001c0001t0003g0106 a0001c0001t0003g0110 |
2 | HG00408.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.1412-306T>C | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 11/11 | chr6 | 169704394 | |||||||
| chr6:169704420 | T | A | 1 | a0001c0001t0001g0092 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1412-332A>T | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 11/11 | chr6 | 169704420 | |||||||
| chr6:169704574 | T | C | 1 | a0001c0001t0002g0027 | 3 | HG01884.hp1 HG02145.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1412-486A>G | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 11/11 | chr6 | 169704574 | |||||||
| chr6:169704617 | A | G | 1 | a0001c0001t0001g0079 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1411+516T>C | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 11/11 | chr6 | 169704617 | |||||||
| chr6:169704907 | C | T | 1 | a0001c0001t0003g0112 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1411+226G>A | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 11/11 | chr6 | 169704907 | |||||||
| chr6:169704961 | T | G | 1 | a0001c0001t0002g0129 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1411+172A>C | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 11/11 | chr6 | 169704961 | |||||||
| chr6:169705014 | A | G | 6 | a0001c0001t0003g0006 a0001c0001t0003g0037 a0001c0001t0003g0041 others(3): Show |
16 | HG01074.hp1 HG02257.hp1 HG02572.hp2 others(13): Show |
intron_variant | MODIFIER | c.1411+119T>C | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 11/11 | chr6 | 169705014 | |||||||
| chr6:169705457 | T | C | 18 | a0001c0001t0002g0151 a0001c0001t0003g0005 a0001c0001t0003g0016 others(15): Show |
46 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(43): Show |
intron_variant | MODIFIER | c.1223-136A>G | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 10/11 | chr6 | 169705457 | |||||||
| chr6:169705757 | C | G | 1 | a0001c0001t0001g0065 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1114-33G>C | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 9/11 | chr6 | 169705757 | |||||||
| chr6:169706085 | GACTT | G | 2 | a0001c0001t0001g0030 a0001c0001t0001g0057 |
3 | HG02071.hp2 NA19057.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.1114-365_1114-362d others(6): Show |
PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 9/11 | chr6 | 169706085 | |||||||
| chr6:169706177 | A | G | 1 | a0001c0001t0003g0096 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1114-453T>C | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 9/11 | chr6 | 169706177 | |||||||
| chr6:169706281 | G | A | 1 | a0001c0001t0003g0037 | 2 | HG02572.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1114-557C>T | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 9/11 | chr6 | 169706281 | |||||||
| chr6:169706323 | CTT | C | 49 | a0001c0001t0001g0007 a0001c0001t0001g0055 a0001c0001t0001g0056 others(46): Show |
118 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(115): Show |
intron_variant | MODIFIER | c.1114-601_1114-600d others(4): Show |
PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 9/11 | chr6 | 169706323 | |||||||
| chr6:169706374 | G | A | 1 | a0001c0001t0001g0066 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1114-650C>T | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 9/11 | chr6 | 169706374 | |||||||
| chr6:169706643 | G | T | 1 | a0001c0001t0001g0064 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1114-919C>A | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 9/11 | chr6 | 169706643 | |||||||
| chr6:169706704 | G | T | 1 | a0001c0001t0003g0105 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1114-980C>A | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 9/11 | chr6 | 169706704 | |||||||
| chr6:169706711 | G | GACAT | 2 | a0001c0001t0002g0021 a0001c0001t0003g0041 |
6 | HG01074.hp1 HG02257.hp1 NA18950.hp1 others(3): Show |
intron_variant | MODIFIER | c.1114-991_1114-988d others(6): Show |
PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 9/11 | chr6 | 169706711 | |||||||
| chr6:169706719 | TACATACA others(9): Show |
T | 1 | a0001c0001t0002g0133 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1114-1011_1114-996 others(19): Show |
PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 9/11 | chr6 | 169706719 | |||||||
| chr6:169706723 | TACATACA others(1): Show |
T | 3 | a0001c0001t0001g0002 a0001c0001t0002g0027 a0001c0001t0006g0125 |
3 | HG00609.hp2 HG01884.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.1114-1007_1114-100 others(12): Show |
PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 9/11 | chr6 | 169706723 | |||||||
| chr6:169706723 | TACATACA others(3): Show |
T | 3 | a0001c0001t0001g0001 a0001c0001t0002g0027 a0001c0001t0006g0126 |
3 | HG01261.hp1 HG02145.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1114-1009_1114-100 others(14): Show |
PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 9/11 | chr6 | 169706723 | |||||||
| chr6:169706723 | TACATACA others(5): Show |
T | 3 | a0001c0001t0001g0060 a0001c0001t0002g0027 a0001c0001t0002g0140 |
3 | HG00639.hp2 HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1114-1011_1114-100 others(16): Show |
PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 9/11 | chr6 | 169706723 | |||||||
| chr6:169706723 | TACATACA others(17): Show |
T | 1 | a0001c0001t0005g0123 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1114-1023_1114-100 others(28): Show |
PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 9/11 | chr6 | 169706723 | |||||||
| chr6:169706727 | T | TACATAC | 3 | a0001c0001t0002g0004 a0001c0001t0002g0152 a0001c0001t0003g0114 |
3 | HG02257.hp2 HG03688.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.1114-1004_1114-100 others(10): Show |
PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 9/11 | chr6 | 169706727 | |||||||
| chr6:169706727 | T | TACATACA others(5): Show |
1 | a0001c0001t0002g0004 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1114-1004_1114-100 others(16): Show |
PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 9/11 | chr6 | 169706727 | |||||||
| chr6:169706727 | TAC | T | 12 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0070 others(9): Show |
22 | HG00597.hp1 HG01109.hp1 HG01175.hp1 others(19): Show |
intron_variant | MODIFIER | c.1114-1005_1114-100 others(6): Show |
PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 9/11 | chr6 | 169706727 | |||||||
| chr6:169706727 | TACAC | T | 13 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0061 others(10): Show |
28 | HG01175.hp2 HG01258.hp1 HG01346.hp2 others(25): Show |
intron_variant | MODIFIER | c.1114-1007_1114-100 others(8): Show |
PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 9/11 | chr6 | 169706727 | |||||||
| chr6:169706727 | TACACAC | T | 28 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(25): Show |
80 | HG00544.hp2 HG00621.hp1 HG00673.hp1 others(77): Show |
intron_variant | MODIFIER | c.1114-1009_1114-100 others(10): Show |
PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 9/11 | chr6 | 169706727 | |||||||
| chr6:169706727 | TACACACA others(1): Show |
T | 22 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(19): Show |
36 | HG00408.hp1 HG00558.hp2 HG01074.hp2 others(33): Show |
intron_variant | MODIFIER | c.1114-1011_1114-100 others(12): Show |
PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 9/11 | chr6 | 169706727 | |||||||
| chr6:169706727 | TACACACA others(3): Show |
T | 37 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0014 others(34): Show |
75 | HG00544.hp1 HG00558.hp1 HG00609.hp1 others(72): Show |
intron_variant | MODIFIER | c.1114-1013_1114-100 others(14): Show |
PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 9/11 | chr6 | 169706727 | |||||||
| chr6:169706727 | TACACACA others(5): Show |
T | 23 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(20): Show |
30 | HG00597.hp2 HG00639.hp1 HG01069.hp1 others(27): Show |
intron_variant | MODIFIER | c.1114-1015_1114-100 others(16): Show |
PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 9/11 | chr6 | 169706727 | |||||||
| chr6:169706727 | TACACACA others(7): Show |
T | 15 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0053 others(12): Show |
16 | HG00438.hp1 HG02083.hp1 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.1114-1017_1114-100 others(18): Show |
PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 9/11 | chr6 | 169706727 | |||||||
| chr6:169706727 | TACACACA others(9): Show |
T | 10 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0015 others(7): Show |
22 | HG01928.hp1 HG01934.hp1 HG01943.hp2 others(19): Show |
intron_variant | MODIFIER | c.1114-1019_1114-100 others(20): Show |
PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 9/11 | chr6 | 169706727 | |||||||
| chr6:169706727 | TACACACA others(11): Show |
T | 18 | a0001c0001t0001g0007 a0001c0001t0001g0055 a0001c0001t0003g0003 others(15): Show |
38 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(35): Show |
intron_variant | MODIFIER | c.1114-1021_1114-100 others(22): Show |
PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 9/11 | chr6 | 169706727 | |||||||
| chr6:169706727 | TACACACA others(13): Show |
T | 2 | a0001c0001t0002g0131 a0001c0001t0003g0115 |
2 | HG02300.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.1114-1023_1114-100 others(24): Show |
PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 9/11 | chr6 | 169706727 | |||||||
| chr6:169706727 | TACACACA others(15): Show |
T | 4 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0002t0002g0045 others(1): Show |
6 | HG01928.hp2 HG02602.hp1 HG03942.hp1 others(3): Show |
intron_variant | MODIFIER | c.1114-1025_1114-100 others(26): Show |
PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 9/11 | chr6 | 169706727 | |||||||
| chr6:169706729 | C | CAT | 3 | a0001c0001t0002g0004 a0001c0001t0002g0048 a0001c0001t0002g0050 |
5 | HG00738.hp1 HG03492.hp1 HG03942.hp2 others(2): Show |
intron_variant | MODIFIER | c.1114-1006_1114-100 others(6): Show |
PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 9/11 | chr6 | 169706729 | |||||||
| chr6:169706731 | C | T | 6 | a0001c0001t0002g0004 a0001c0001t0002g0017 a0001c0001t0002g0022 others(3): Show |
9 | HG00099.hp2 HG01070.hp1 HG01081.hp2 others(6): Show |
intron_variant | MODIFIER | c.1114-1007G>A | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 9/11 | chr6 | 169706731 | |||||||
| chr6:169706733 | C | T | 8 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0047 others(5): Show |
18 | HG01109.hp1 HG01192.hp1 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.1114-1009G>A | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 9/11 | chr6 | 169706733 | |||||||
| chr6:169706735 | C | T | 6 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0017 others(3): Show |
12 | HG01346.hp2 HG01515.hp1 HG01515.hp2 others(9): Show |
intron_variant | MODIFIER | c.1114-1011G>A | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 9/11 | chr6 | 169706735 | |||||||
| chr6:169706737 | C | T | 4 | a0001c0001t0002g0132 a0001c0001t0003g0006 a0001c0001t0003g0111 others(1): Show |
12 | HG01168.hp2 NA18947.hp2 NA18948.hp1 others(9): Show |
intron_variant | MODIFIER | c.1114-1013G>A | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 9/11 | chr6 | 169706737 | |||||||
| chr6:169706739 | C | T | 1 | a0001c0001t0002g0141 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1114-1015G>A | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 9/11 | chr6 | 169706739 | |||||||
| chr6:169706751 | C | T | 1 | a0001c0001t0002g0131 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1114-1027G>A | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 9/11 | chr6 | 169706751 | |||||||
| chr6:169706757 | C | A | 1 | a0001c0001t0001g0057 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1114-1033G>T | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 9/11 | chr6 | 169706757 | |||||||
| chr6:169706781 | T | C | 2 | a0001c0001t0001g0053 a0001c0001t0001g0054 |
2 | HG02647.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1114-1057A>G | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 9/11 | chr6 | 169706781 | |||||||
| chr6:169706907 | T | C | 1 | a0001c0001t0001g0032 | 2 | NA18997.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.1114-1183A>G | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 9/11 | chr6 | 169706907 | |||||||
| chr6:169707186 | CTGTA | C | 2 | a0001c0001t0003g0040 a0001c0001t0003g0117 |
3 | HG02970.hp2 HG03579.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1114-1466_1114-146 others(8): Show |
PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 9/11 | chr6 | 169707186 | |||||||
| chr6:169707205 | C | A | 1 | a0001c0001t0003g0109 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1114-1481G>T | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 9/11 | chr6 | 169707205 | |||||||
| chr6:169707324 | A | C | 1 | a0001c0001t0001g0013 | 5 | HG02109.hp2 HG02486.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1114-1600T>G | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 9/11 | chr6 | 169707324 | |||||||
| chr6:169707543 | T | TTA | 1 | a0001c0001t0002g0023 | 4 | HG02723.hp1 HG02886.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1114-1820_1114-181 others(6): Show |
PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 9/11 | chr6 | 169707543 | |||||||
| chr6:169707606 | C | T | 50 | a0001c0001t0001g0007 a0001c0001t0001g0055 a0001c0001t0001g0056 others(47): Show |
119 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(116): Show |
intron_variant | MODIFIER | c.1114-1882G>A | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 9/11 | chr6 | 169707606 | |||||||
| chr6:169708043 | A | C | 1 | a0001c0001t0016g0158 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1113+2193T>G | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 9/11 | chr6 | 169708043 | |||||||
| chr6:169708071 | T | C | 1 | a0001c0001t0001g0087 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1113+2165A>G | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 9/11 | chr6 | 169708071 | |||||||
| chr6:169708238 | G | A | 1 | a0001c0001t0001g0067 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1113+1998C>T | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 9/11 | chr6 | 169708238 | |||||||
| chr6:169708267 | G | A | 49 | a0001c0001t0001g0007 a0001c0001t0001g0055 a0001c0001t0001g0056 others(46): Show |
118 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(115): Show |
intron_variant | MODIFIER | c.1113+1969C>T | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 9/11 | chr6 | 169708267 | |||||||
| chr6:169708321 | C | G | 54 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(51): Show |
149 | HG00408.hp1 HG00544.hp1 HG00544.hp2 others(146): Show |
intron_variant | MODIFIER | c.1113+1915G>C | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 9/11 | chr6 | 169708321 | |||||||
| chr6:169708344 | T | G | 32 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(29): Show |
114 | HG00408.hp1 HG00544.hp1 HG00544.hp2 others(111): Show |
intron_variant | MODIFIER | c.1113+1892A>C | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 9/11 | chr6 | 169708344 | |||||||
| chr6:169708385 | G | A | 2 | a0001c0001t0004g0155 a0001c0001t0004g0156 |
2 | NA18945.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.1113+1851C>T | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 9/11 | chr6 | 169708385 | |||||||
| chr6:169708416 | T | C | 1 | a0001c0001t0003g0043 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1113+1820A>G | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 9/11 | chr6 | 169708416 | |||||||
| chr6:169708521 | A | T | 1 | a0001c0001t0001g0055 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1113+1715T>A | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 9/11 | chr6 | 169708521 | |||||||
| chr6:169708593 | T | C | 54 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(51): Show |
149 | HG00408.hp1 HG00544.hp1 HG00544.hp2 others(146): Show |
intron_variant | MODIFIER | c.1113+1643A>G | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 9/11 | chr6 | 169708593 | |||||||
| chr6:169708690 | T | C | 1 | a0001c0001t0001g0085 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1113+1546A>G | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 9/11 | chr6 | 169708690 | |||||||
| chr6:169708703 | C | T | 136 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(133): Show |
335 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(332): Show |
intron_variant | MODIFIER | c.1113+1533G>A | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 9/11 | chr6 | 169708703 | |||||||
| chr6:169708705 | G | A | 1 | a0001c0001t0001g0056 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1113+1531C>T | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 9/11 | chr6 | 169708705 | |||||||
| chr6:169708762 | C | T | 1 | a0001c0001t0001g0074 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1113+1474G>A | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 9/11 | chr6 | 169708762 | |||||||
| chr6:169708823 | T | C | 1 | a0001c0001t0002g0027 | 3 | HG01884.hp1 HG02145.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1113+1413A>G | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 9/11 | chr6 | 169708823 | |||||||
| chr6:169708916 | T | C | 1 | a0001c0001t0001g0081 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1113+1320A>G | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 9/11 | chr6 | 169708916 | |||||||
| chr6:169708917 | T | C | 1 | a0001c0001t0003g0107 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1113+1319A>G | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 9/11 | chr6 | 169708917 | |||||||
| chr6:169708971 | G | A | 34 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(31): Show |
116 | HG00408.hp1 HG00544.hp1 HG00544.hp2 others(113): Show |
intron_variant | MODIFIER | c.1113+1265C>T | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 9/11 | chr6 | 169708971 | |||||||
| chr6:169709088 | T | A | 49 | a0001c0001t0001g0007 a0001c0001t0001g0055 a0001c0001t0001g0056 others(46): Show |
118 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(115): Show |
intron_variant | MODIFIER | c.1113+1148A>T | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 9/11 | chr6 | 169709088 | |||||||
| chr6:169709122 | A | G | 1 | a0001c0002t0002g0128 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1113+1114T>C | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 9/11 | chr6 | 169709122 | |||||||
| chr6:169709303 | CTT | C | 18 | a0001c0001t0002g0151 a0001c0001t0003g0005 a0001c0001t0003g0016 others(15): Show |
46 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(43): Show |
intron_variant | MODIFIER | c.1113+931_1113+932d others(4): Show |
PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 9/11 | chr6 | 169709303 | |||||||
| chr6:169709604 | G | T | 54 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(51): Show |
149 | HG00408.hp1 HG00544.hp1 HG00544.hp2 others(146): Show |
intron_variant | MODIFIER | c.1113+632C>A | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 9/11 | chr6 | 169709604 | |||||||
| chr6:169710147 | G | A | 18 | a0001c0001t0001g0001 a0001c0001t0001g0024 a0001c0001t0001g0032 others(15): Show |
59 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.1113+89C>T | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 9/11 | chr6 | 169710147 | |||||||
| chr6:169710429 | T | A | 1 | a0001c0002t0002g0145 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.958-38A>T | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 8/11 | chr6 | 169710429 | |||||||
| chr6:169710791 | A | G | 1 | a0001c0001t0002g0130 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.958-400T>C | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 8/11 | chr6 | 169710791 | |||||||
| chr6:169710803 | G | A | 1 | a0001c0001t0001g0068 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.958-412C>T | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 8/11 | chr6 | 169710803 | |||||||
| chr6:169710839 | G | GA | 6 | a0001c0001t0003g0006 a0001c0001t0003g0037 a0001c0001t0003g0041 others(3): Show |
16 | HG01074.hp1 HG02257.hp1 HG02572.hp2 others(13): Show |
intron_variant | MODIFIER | c.958-449dupT | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 8/11 | chr6 | 169710839 | |||||||
| chr6:169711222 | C | G | 1 | a0001c0001t0001g0063 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.958-831G>C | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 8/11 | chr6 | 169711222 | |||||||
| chr6:169711505 | G | A | 21 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0031 others(18): Show |
34 | HG01070.hp2 HG01071.hp2 HG01361.hp2 others(31): Show |
intron_variant | MODIFIER | c.957+881C>T | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 8/11 | chr6 | 169711505 | |||||||
| chr6:169711670 | T | C | 1 | a0001c0001t0001g0013 | 5 | HG02109.hp2 HG02486.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.957+716A>G | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 8/11 | chr6 | 169711670 | |||||||
| chr6:169711697 | G | A | 2 | a0001c0001t0006g0125 a0001c0001t0006g0126 |
2 | HG02258.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.957+689C>T | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 8/11 | chr6 | 169711697 | |||||||
| chr6:169711889 | G | C | 108 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(105): Show |
272 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(269): Show |
intron_variant | MODIFIER | c.957+497C>G | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 8/11 | chr6 | 169711889 | |||||||
| chr6:169711936 | C | CA | 5 | a0001c0001t0003g0006 a0001c0001t0003g0041 a0001c0001t0003g0100 others(2): Show |
14 | HG01074.hp1 HG02257.hp1 HG03688.hp2 others(11): Show |
intron_variant | MODIFIER | c.957+449dupT | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 8/11 | chr6 | 169711936 | |||||||
| chr6:169711994 | ATATTTTC others(62): Show |
A | 1 | a0004c0004t0003g0097 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.957+323_957+391del others(69): Show |
PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 8/11 | chr6 | 169711994 | |||||||
| chr6:169712023 | G | A | 5 | a0001c0001t0003g0006 a0001c0001t0003g0041 a0001c0001t0003g0100 others(2): Show |
14 | HG01074.hp1 HG02257.hp1 HG03688.hp2 others(11): Show |
intron_variant | MODIFIER | c.957+363C>T | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 8/11 | chr6 | 169712023 | |||||||
| chr6:169712303 | A | G | 1 | a0001c0001t0001g0062 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.957+83T>C | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 8/11 | chr6 | 169712303 | |||||||
| chr6:169712797 | A | G | 1 | a0001c0001t0003g0102 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.804-258T>C | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 7/11 | chr6 | 169712797 | |||||||
| chr6:169712882 | C | G | 1 | a0001c0001t0003g0101 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.804-343G>C | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 7/11 | chr6 | 169712882 | |||||||
| chr6:169712934 | C | T | 1 | a0001c0001t0001g0084 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.804-395G>A | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 7/11 | chr6 | 169712934 | |||||||
| chr6:169713148 | C | A | 50 | a0001c0001t0001g0007 a0001c0001t0001g0055 a0001c0001t0001g0056 others(47): Show |
119 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(116): Show |
intron_variant | MODIFIER | c.804-609G>T | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 7/11 | chr6 | 169713148 | |||||||
| chr6:169713199 | A | G | 139 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(136): Show |
342 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(339): Show |
intron_variant | MODIFIER | c.804-660T>C | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 7/11 | chr6 | 169713199 | |||||||
| chr6:169713234 | C | T | 2 | a0001c0001t0006g0125 a0001c0001t0006g0126 |
2 | HG02258.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.804-695G>A | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 7/11 | chr6 | 169713234 | |||||||
| chr6:169713317 | G | A | 1 | a0001c0001t0001g0090 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.804-778C>T | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 7/11 | chr6 | 169713317 | |||||||
| chr6:169713356 | C | T | 4 | a0001c0001t0003g0020 a0001c0001t0003g0042 a0001c0001t0003g0119 others(1): Show |
9 | HG00738.hp2 HG01069.hp2 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.804-817G>A | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 7/11 | chr6 | 169713356 | |||||||
| chr6:169713388 | C | A | 1 | a0001c0001t0001g0060 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.804-849G>T | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 7/11 | chr6 | 169713388 | |||||||
| chr6:169713397 | G | A | 11 | a0001c0001t0003g0005 a0001c0001t0003g0025 a0001c0001t0003g0036 others(8): Show |
32 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(29): Show |
intron_variant | MODIFIER | c.804-858C>T | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 7/11 | chr6 | 169713397 | |||||||
| chr6:169713428 | G | A | 1 | a0001c0001t0003g0112 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.804-889C>T | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 7/11 | chr6 | 169713428 | |||||||
| chr6:169713510 | G | A | 21 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0031 others(18): Show |
34 | HG01070.hp2 HG01071.hp2 HG01361.hp2 others(31): Show |
intron_variant | MODIFIER | c.804-971C>T | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 7/11 | chr6 | 169713510 | |||||||
| chr6:169713577 | C | T | 1 | a0001c0002t0002g0144 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.804-1038G>A | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 7/11 | chr6 | 169713577 | |||||||
| chr6:169713598 | C | CA | 5 | a0001c0001t0001g0086 a0001c0001t0002g0017 a0001c0001t0002g0135 others(2): Show |
9 | HG01981.hp1 HG02280.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.804-1060dupT | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 7/11 | chr6 | 169713598 | |||||||
| chr6:169713598 | CA | C | 12 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(9): Show |
12 | HG02258.hp2 HG02615.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.804-1060delT | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 7/11 | chr6 | 169713598 | |||||||
| chr6:169713616 | A | T | 2 | a0001c0001t0001g0092 a0001c0001t0002g0046 |
3 | HG02895.hp1 HG02976.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.804-1077T>A | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 7/11 | chr6 | 169713616 | |||||||
| chr6:169713867 | T | C | 13 | a0001c0001t0003g0103 a0001c0001t0016g0158 a0001c0002t0002g0008 others(10): Show |
25 | HG00639.hp1 HG01934.hp2 HG02004.hp1 others(22): Show |
intron_variant | MODIFIER | c.803+866A>G | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 7/11 | chr6 | 169713867 | |||||||
| chr6:169713983 | G | A | 2 | a0001c0001t0006g0125 a0001c0001t0006g0126 |
2 | HG02258.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.803+750C>T | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 7/11 | chr6 | 169713983 | |||||||
| chr6:169714043 | C | G | 1 | a0001c0001t0001g0082 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.803+690G>C | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 7/11 | chr6 | 169714043 | |||||||
| chr6:169714067 | G | A | 23 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(20): Show |
40 | HG01070.hp2 HG01071.hp2 HG01361.hp2 others(37): Show |
intron_variant | MODIFIER | c.803+666C>T | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 7/11 | chr6 | 169714067 | |||||||
| chr6:169714117 | C | CA | 4 | a0001c0001t0001g0015 a0001c0001t0001g0087 a0001c0001t0002g0046 others(1): Show |
10 | HG01928.hp1 HG01943.hp2 HG01952.hp2 others(7): Show |
intron_variant | MODIFIER | c.803+615dupT | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 7/11 | chr6 | 169714117 | |||||||
| chr6:169714398 | T | G | 6 | a0001c0001t0003g0006 a0001c0001t0003g0037 a0001c0001t0003g0041 others(3): Show |
16 | HG01074.hp1 HG02257.hp1 HG02572.hp2 others(13): Show |
intron_variant | MODIFIER | c.803+335A>C | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 7/11 | chr6 | 169714398 | |||||||
| chr6:169714400 | C | A | 1 | a0001c0001t0016g0158 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.803+333G>T | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 7/11 | chr6 | 169714400 | |||||||
| chr6:169714455 | C | A | 1 | a0001c0001t0004g0028 | 3 | HG01069.hp1 HG02280.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.803+278G>T | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 7/11 | chr6 | 169714455 | |||||||
| chr6:169714574 | A | G | 48 | a0001c0001t0001g0007 a0001c0001t0001g0055 a0001c0001t0001g0056 others(45): Show |
117 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(114): Show |
intron_variant | MODIFIER | c.803+159T>C | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 7/11 | chr6 | 169714574 | |||||||
| chr6:169714601 | T | C | 1 | a0001c0001t0001g0069 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.803+132A>G | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 7/11 | chr6 | 169714601 | |||||||
| chr6:169714613 | T | C | 3 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 |
3 | NA18940.hp1 NA19072.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.803+120A>G | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 7/11 | chr6 | 169714613 | |||||||
| chr6:169714625 | T | C | 1 | a0001c0001t0001g0070 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.803+108A>G | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 7/11 | chr6 | 169714625 | |||||||
| chr6:169714940 | C | T | 1 | a0001c0001t0002g0050 | 2 | HG00738.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.694-98G>A | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 6/11 | chr6 | 169714940 | |||||||
| chr6:169715118 | C | T | 1 | a0001c0001t0001g0078 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.694-276G>A | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 6/11 | chr6 | 169715118 | |||||||
| chr6:169715196 | T | TA | 2 | a0001c0001t0002g0023 a0001c0001t0002g0147 |
5 | HG02723.hp1 HG02886.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.694-355dupT | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 6/11 | chr6 | 169715196 | |||||||
| chr6:169715412 | A | G | 1 | a0001c0001t0001g0061 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.693+296T>C | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 6/11 | chr6 | 169715412 | |||||||
| chr6:169715482 | G | A | 4 | a0001c0001t0005g0123 a0001c0001t0006g0124 a0001c0001t0006g0125 others(1): Show |
4 | HG02258.hp2 HG02886.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.693+226C>T | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 6/11 | chr6 | 169715482 | |||||||
| chr6:169715591 | C | A | 1 | a0001c0001t0003g0096 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.693+117G>T | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 6/11 | chr6 | 169715591 | |||||||
| chr6:169715591 | CA | C | 12 | a0001c0001t0001g0072 a0001c0001t0003g0005 a0001c0001t0003g0025 others(9): Show |
33 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(30): Show |
intron_variant | MODIFIER | c.693+116delT | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 6/11 | chr6 | 169715591 | |||||||
| chr6:169715598 | A | C | 1 | a0001c0001t0001g0054 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.693+110T>G | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 6/11 | chr6 | 169715598 | |||||||
| chr6:169715630 | G | C | 1 | a0001c0001t0003g0037 | 2 | HG02572.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.693+78C>G | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 6/11 | chr6 | 169715630 | |||||||
| chr6:169715683 | G | A | 4 | a0001c0001t0005g0123 a0001c0001t0006g0124 a0001c0001t0006g0125 others(1): Show |
4 | HG02258.hp2 HG02886.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.693+25C>T | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 6/11 | chr6 | 169715683 | |||||||
| chr6:169716129 | TAAGG | T | 1 | a0001c0001t0002g0022 | 4 | HG02630.hp1 HG02723.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.410-45_410-42delCC others(2): Show |
PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 4/11 | chr6 | 169716129 | |||||||
| chr6:169716140 | G | A | 1 | a0001c0001t0001g0034 | 2 | HG02145.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.410-52C>T | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 4/11 | chr6 | 169716140 | |||||||
| chr6:169716460 | T | C | 1 | a0001c0001t0003g0116 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.410-372A>G | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 4/11 | chr6 | 169716460 | |||||||
| chr6:169716529 | C | T | 1 | a0001c0001t0002g0049 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.410-441G>A | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 4/11 | chr6 | 169716529 | |||||||
| chr6:169716869 | C | T | 1 | a0001c0001t0003g0025 | 3 | HG02132.hp2 NA19086.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.410-781G>A | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 4/11 | chr6 | 169716869 | |||||||
| chr6:169716888 | C | T | 1 | a0001c0001t0006g0124 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.410-800G>A | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 4/11 | chr6 | 169716888 | |||||||
| chr6:169716926 | A | G | 1 | a0001c0001t0001g0059 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.410-838T>C | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 4/11 | chr6 | 169716926 | |||||||
| chr6:169717030 | G | A | 1 | a0001c0001t0003g0112 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.409+793C>T | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 4/11 | chr6 | 169717030 | |||||||
| chr6:169717056 | A | G | 1 | a0001c0001t0003g0038 | 2 | NA18944.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.409+767T>C | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 4/11 | chr6 | 169717056 | |||||||
| chr6:169717073 | A | G | 109 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(106): Show |
274 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(271): Show |
intron_variant | MODIFIER | c.409+750T>C | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 4/11 | chr6 | 169717073 | |||||||
| chr6:169717133 | T | G | 1 | a0001c0001t0001g0071 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.409+690A>C | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 4/11 | chr6 | 169717133 | |||||||
| chr6:169717277 | A | C | 1 | a0001c0001t0003g0100 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.409+546T>G | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 4/11 | chr6 | 169717277 | |||||||
| chr6:169717342 | A | G | 2 | a0001c0001t0002g0027 a0001c0001t0002g0140 |
4 | HG00639.hp2 HG01884.hp1 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.409+481T>C | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 4/11 | chr6 | 169717342 | |||||||
| chr6:169717347 | G | A | 1 | a0001c0001t0016g0158 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.409+476C>T | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 4/11 | chr6 | 169717347 | |||||||
| chr6:169717500 | T | A | 5 | a0001c0001t0001g0010 a0001c0001t0001g0072 a0001c0001t0001g0073 others(2): Show |
10 | HG00544.hp2 HG00673.hp2 NA18947.hp1 others(7): Show |
intron_variant | MODIFIER | c.409+323A>T | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 4/11 | chr6 | 169717500 | |||||||
| chr6:169717514 | T | C | 1 | a0001c0006t0001g0077 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.409+309A>G | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 4/11 | chr6 | 169717514 | |||||||
| chr6:169718157 | T | C | 1 | a0001c0001t0001g0091 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.326-251A>G | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 3/11 | chr6 | 169718157 | |||||||
| chr6:169718187 | G | A | 1 | a0001c0001t0003g0113 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.326-281C>T | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 3/11 | chr6 | 169718187 | |||||||
| chr6:169718388 | G | A | 1 | a0001c0002t0002g0146 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.325+400C>T | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 3/11 | chr6 | 169718388 | |||||||
| chr6:169718394 | G | A | 1 | a0001c0001t0003g0114 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.325+394C>T | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 3/11 | chr6 | 169718394 | |||||||
| chr6:169718560 | C | G | 1 | a0001c0002t0002g0139 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.325+228G>C | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 3/11 | chr6 | 169718560 | |||||||
| chr6:169718577 | G | C | 1 | a0001c0001t0001g0053 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.325+211C>G | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 3/11 | chr6 | 169718577 | |||||||
| chr6:169718611 | T | C | 1 | a0001c0001t0001g0075 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.325+177A>G | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 3/11 | chr6 | 169718611 | |||||||
| chr6:169718632 | C | T | 1 | a0001c0001t0001g0060 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.325+156G>A | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 3/11 | chr6 | 169718632 | |||||||
| chr6:169718633 | G | A | 1 | a0001c0001t0001g0076 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.325+155C>T | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 3/11 | chr6 | 169718633 | |||||||
| chr6:169718659 | C | A | 2 | a0001c0001t0003g0115 a0001c0001t0003g0116 |
2 | NA19070.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.325+129G>T | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 3/11 | chr6 | 169718659 | |||||||
| chr6:169718664 | A | C | 1 | a0001c0006t0001g0077 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.325+124T>G | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 3/11 | chr6 | 169718664 | |||||||
| chr6:169718934 | CA | C | 2 | a0001c0001t0002g0048 a0001c0001t0014g0154 |
3 | HG01168.hp2 HG03492.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.195-17delT | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 2/11 | chr6 | 169718934 | |||||||
| chr6:169718935 | A | T | 12 | a0001c0002t0002g0008 a0001c0002t0002g0012 a0001c0002t0002g0045 others(9): Show |
24 | HG00639.hp1 HG01934.hp2 HG02080.hp2 others(21): Show |
intron_variant | MODIFIER | c.195-17T>A | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 2/11 | chr6 | 169718935 | |||||||
| chr6:169718998 | A | G | 5 | a0001c0001t0004g0009 a0001c0001t0004g0028 a0001c0001t0004g0155 others(2): Show |
13 | HG00438.hp1 HG00597.hp2 HG01069.hp1 others(10): Show |
intron_variant | MODIFIER | c.195-80T>C | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 2/11 | chr6 | 169718998 | |||||||
| chr6:169719071 | G | C | 1 | a0001c0001t0003g0037 | 2 | HG02572.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.195-153C>G | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 2/11 | chr6 | 169719071 | |||||||
| chr6:169719154 | T | C | 3 | a0001c0001t0002g0019 a0001c0001t0002g0023 a0001c0001t0002g0147 |
10 | HG02572.hp1 HG02723.hp1 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.195-236A>G | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 2/11 | chr6 | 169719154 | |||||||
| chr6:169719176 | G | A | 1 | a0001c0001t0016g0158 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.195-258C>T | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 2/11 | chr6 | 169719176 | |||||||
| chr6:169719195 | A | G | 139 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(136): Show |
342 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(339): Show |
intron_variant | MODIFIER | c.195-277T>C | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 2/11 | chr6 | 169719195 | |||||||
| chr6:169719274 | A | G | 1 | a0001c0001t0001g0013 | 5 | HG02109.hp2 HG02486.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.195-356T>C | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 2/11 | chr6 | 169719274 | |||||||
| chr6:169719297 | C | T | 1 | a0001c0001t0001g0059 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.195-379G>A | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 2/11 | chr6 | 169719297 | |||||||
| chr6:169719370 | T | A | 1 | a0001c0001t0002g0135 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.195-452A>T | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 2/11 | chr6 | 169719370 | |||||||
| chr6:169719393 | C | T | 30 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(27): Show |
108 | HG00408.hp1 HG00544.hp1 HG00544.hp2 others(105): Show |
intron_variant | MODIFIER | c.195-475G>A | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 2/11 | chr6 | 169719393 | |||||||
| chr6:169719394 | G | GT | 4 | a0001c0001t0005g0123 a0001c0001t0006g0124 a0001c0001t0006g0125 others(1): Show |
4 | HG02258.hp2 HG02886.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.195-477dupA | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 2/11 | chr6 | 169719394 | |||||||
| chr6:169719578 | A | C | 1 | a0001c0001t0003g0037 | 2 | HG02572.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.195-660T>G | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 2/11 | chr6 | 169719578 | |||||||
| chr6:169719635 | C | G | 1 | a0001c0001t0001g0058 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.195-717G>C | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 2/11 | chr6 | 169719635 | |||||||
| chr6:169719718 | G | C | 1 | a0001c0006t0001g0077 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.195-800C>G | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 2/11 | chr6 | 169719718 | |||||||
| chr6:169719827 | A | C | 1 | a0001c0001t0001g0057 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.195-909T>G | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 2/11 | chr6 | 169719827 | |||||||
| chr6:169719898 | A | G | 1 | a0001c0001t0003g0098 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.195-980T>C | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 2/11 | chr6 | 169719898 | |||||||
| chr6:169719973 | C | CA | 53 | a0001c0001t0001g0007 a0001c0001t0001g0054 a0001c0001t0001g0055 others(50): Show |
122 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(119): Show |
intron_variant | MODIFIER | c.194+1031dupT | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 2/11 | chr6 | 169719973 | |||||||
| chr6:169720142 | T | C | 4 | a0001c0001t0005g0123 a0001c0001t0006g0124 a0001c0001t0006g0125 others(1): Show |
4 | HG02258.hp2 HG02886.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.194+863A>G | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 2/11 | chr6 | 169720142 | |||||||
| chr6:169720389 | G | A | 1 | a0001c0001t0003g0117 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.194+616C>T | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 2/11 | chr6 | 169720389 | |||||||
| chr6:169720518 | T | C | 1 | a0001c0001t0016g0158 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.194+487A>G | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 2/11 | chr6 | 169720518 | |||||||
| chr6:169720535 | G | A | 1 | a0001c0001t0003g0118 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.194+470C>T | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 2/11 | chr6 | 169720535 | |||||||
| chr6:169720723 | A | G | 3 | a0001c0001t0002g0018 a0001c0001t0013g0153 a0001c0001t0017g0159 |
7 | HG01109.hp2 HG02258.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.194+282T>C | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 2/11 | chr6 | 169720723 | |||||||
| chr6:169720789 | G | A | 3 | a0001c0001t0001g0035 a0001c0001t0001g0092 a0001c0001t0010g0094 |
4 | HG02895.hp1 HG03225.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.194+216C>T | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 2/11 | chr6 | 169720789 | |||||||
| chr6:169720831 | C | T | 139 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(136): Show |
342 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(339): Show |
intron_variant | MODIFIER | c.194+174G>A | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 2/11 | chr6 | 169720831 | |||||||
| chr6:169721265 | C | T | 1 | a0001c0001t0001g0033 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.88-154G>A | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 1/11 | chr6 | 169721265 | |||||||
| chr6:169721481 | G | A | 1 | a0001c0001t0001g0032 | 2 | NA18997.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.88-370C>T | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 1/11 | chr6 | 169721481 | |||||||
| chr6:169721559 | A | G | 2 | a0001c0001t0003g0036 a0004c0004t0003g0097 |
3 | NA18970.hp2 NA19012.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.88-448T>C | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 1/11 | chr6 | 169721559 | |||||||
| chr6:169721645 | C | A | 1 | a0001c0001t0001g0080 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.88-534G>T | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 1/11 | chr6 | 169721645 | |||||||
| chr6:169721685 | T | A | 1 | a0001c0001t0003g0119 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.88-574A>T | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 1/11 | chr6 | 169721685 | |||||||
| chr6:169721691 | A | AGAG | 48 | a0001c0001t0001g0007 a0001c0001t0001g0055 a0001c0001t0001g0056 others(45): Show |
117 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(114): Show |
intron_variant | MODIFIER | c.88-581_88-580insCT others(1): Show |
PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 1/11 | chr6 | 169721691 | |||||||
| chr6:169721691 | A | G | 1 | a0001c0001t0003g0119 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.88-580T>C | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 1/11 | chr6 | 169721691 | |||||||
| chr6:169721693 | A | G | 1 | a0001c0002t0002g0138 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.88-582T>C | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 1/11 | chr6 | 169721693 | |||||||
| chr6:169722138 | G | A | 156 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(153): Show |
386 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(383): Show |
intron_variant | MODIFIER | c.88-1027C>T | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 1/11 | chr6 | 169722138 | |||||||
| chr6:169722328 | A | G | 1 | a0001c0001t0003g0096 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.88-1217T>C | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 1/11 | chr6 | 169722328 | |||||||
| chr6:169722410 | T | C | 1 | a0001c0001t0002g0136 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.88-1299A>G | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 1/11 | chr6 | 169722410 | |||||||
| chr6:169722419 | T | C | 2 | a0001c0001t0001g0024 a0001c0001t0001g0081 |
4 | HG00673.hp1 NA18942.hp2 NA18965.hp2 others(1): Show |
intron_variant | MODIFIER | c.88-1308A>G | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 1/11 | chr6 | 169722419 | |||||||
| chr6:169722607 | G | C | 22 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0033 others(19): Show |
34 | HG01070.hp2 HG01071.hp2 HG01361.hp2 others(31): Show |
intron_variant | MODIFIER | c.87+1238C>G | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 1/11 | chr6 | 169722607 | |||||||
| chr6:169722711 | C | T | 2 | a0001c0001t0001g0053 a0001c0001t0001g0054 |
2 | HG02647.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.87+1134G>A | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 1/11 | chr6 | 169722711 | |||||||
| chr6:169722958 | T | C | 1 | a0001c0001t0003g0042 | 2 | HG00738.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.87+887A>G | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 1/11 | chr6 | 169722958 | |||||||
| chr6:169723098 | G | A | 1 | a0001c0001t0002g0137 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.87+747C>T | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 1/11 | chr6 | 169723098 | |||||||
| chr6:169723100 | G | A | 138 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(135): Show |
340 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(337): Show |
intron_variant | MODIFIER | c.87+745C>T | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 1/11 | chr6 | 169723100 | |||||||
| chr6:169723390 | T | C | 1 | a0001c0001t0002g0149 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.87+455A>G | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 1/11 | chr6 | 169723390 | |||||||
| chr6:169723484 | C | G | 107 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(104): Show |
271 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(268): Show |
intron_variant | MODIFIER | c.87+361G>C | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 1/11 | chr6 | 169723484 | |||||||
| chr6:169723539 | G | A | 1 | a0001c0002t0002g0150 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.87+306C>T | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 1/11 | chr6 | 169723539 | |||||||
| chr6:169723581 | G | C | 3 | a0001c0001t0002g0151 a0001c0001t0003g0016 a0001c0001t0003g0043 |
8 | HG00735.hp1 HG02559.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.87+264C>G | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 1/11 | chr6 | 169723581 | |||||||
| chr6:169723642 | G | T | 1 | a0001c0001t0002g0046 | 2 | HG02976.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.87+203C>A | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 1/11 | chr6 | 169723642 | |||||||
| chr6:169723729 | C | G | 2 | a0001c0002t0002g0045 a0001c0002t0002g0128 |
3 | NA18981.hp2 NA18995.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.87+116G>C | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 1/11 | chr6 | 169723729 | |||||||
| chr6:169723809 | G | C | 1 | a0001c0001t0006g0126 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.87+36C>G | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 1/11 | chr6 | 169723809 | |||||||
| chr6:169723819 | T | A | 1 | a0001c0001t0002g0152 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.87+26A>T | PHF10 | ENSG00000130024.15 | transcript | ENST00000339209.9 | protein_coding | 1/11 | chr6 | 169723819 |