Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 51131 |
| ensemblid | ENSG00000136147.18 |
| hgncid | 17024 |
| symbol | PHF11 |
| name | PHD finger protein 11 |
| refseq_nuc | NM_001040443.3 |
| refseq_prot | NP_001035533.1 |
| ensembl_nuc | ENST00000378319.8 |
| ensembl_prot | ENSP00000367570.3 |
| mane_status | MANE Select |
| chr | chr13 |
| start | 49495953 |
| end | 49528976 |
| strand | + |
| ver | v1.2 |
| region | chr13:49495953-49528976 |
| region5000 | chr13:49490953-49533976 |
| regionname0 | PHF11_chr13_49495953_49528976 |
| regionname5000 | PHF11_chr13_49490953_49533976 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 331 | 405 | 84 | 76 | 187 | 14 | 42 | 141 | PHF11_chr13_49490953_49533976 | PHF11 | MAQAS others(326): Show |
chr13 | 49490953 | 49533976 |
| a0002 | 0/0 | 324 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | MAERV others(319): Show |
chr13 | 49490953 | 49533976 |
| a0003 | 0/0 | 331 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | MAQAS others(326): Show |
chr13 | 49490953 | 49533976 |
| a0004 | 0/0 | 331 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | MAQAS others(326): Show |
chr13 | 49490953 | 49533976 |
| a0005 | 0/0 | 331 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PHF11_chr13_49490953_49533976 | PHF11 | MAQAS others(326): Show |
chr13 | 49490953 | 49533976 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 993 | 327 | 77 | 48 | 161 | 8 | 32 | PHF11_chr13_49490953_49533976 | PHF11 | ATGGC others(988): Show |
chr13 | 49490953 | 49533976 | ||
| a0001c0002 | 1/0 | 993 | 74 | 7 | 26 | 24 | 6 | 10 | PHF11_chr13_49490953_49533976 | PHF11 | ATGGC others(988): Show |
chr13 | 49490953 | 49533976 | ||
| a0001c0004 | 0/0 | 993 | 2 | 0 | 2 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | ATGGC others(988): Show |
chr13 | 49490953 | 49533976 | ||
| a0001c0005 | 0/0 | 993 | 2 | 0 | 0 | 2 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | ATGGC others(988): Show |
chr13 | 49490953 | 49533976 | ||
| a0002c0003 | 0/0 | 972 | 5 | 5 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | ATGGC others(967): Show |
chr13 | 49490953 | 49533976 | ||
| a0003c0006 | 0/0 | 993 | 2 | 2 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | ATGGC others(988): Show |
chr13 | 49490953 | 49533976 | ||
| a0004c0007 | 0/0 | 993 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | ATGGC others(988): Show |
chr13 | 49490953 | 49533976 | ||
| a0005c0008 | 0/0 | 993 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | ATGGC others(988): Show |
chr13 | 49490953 | 49533976 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 1356 | 107 | 44 | 15 | 36 | 0 | 12 | PHF11_chr13_49490953_49533976 | PHF11 | ACTTC others(1351): Show |
chr13 | 49490953 | 49533976 |
| a0001c0001t0002 | 0/1 | 1356 | 170 | 31 | 30 | 87 | 7 | 14 | PHF11_chr13_49490953_49533976 | PHF11 | ACTTC others(1351): Show |
chr13 | 49490953 | 49533976 |
| a0001c0001t0003 | 0/0 | 1359 | 49 | 1 | 3 | 38 | 1 | 6 | PHF11_chr13_49490953_49533976 | PHF11 | ACTTC others(1354): Show |
chr13 | 49490953 | 49533976 |
| a0001c0001t0004 | 0/0 | 1356 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | ACTTC others(1351): Show |
chr13 | 49490953 | 49533976 |
| a0001c0002t0001 | 1/0 | 1356 | 69 | 6 | 22 | 24 | 6 | 10 | PHF11_chr13_49490953_49533976 | PHF11 | ACTTC others(1351): Show |
chr13 | 49490953 | 49533976 |
| a0001c0002t0002 | 0/0 | 1356 | 5 | 1 | 4 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | ACTTC others(1351): Show |
chr13 | 49490953 | 49533976 |
| a0001c0004t0002 | 0/0 | 1356 | 2 | 0 | 2 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | ACTTC others(1351): Show |
chr13 | 49490953 | 49533976 |
| a0001c0005t0002 | 0/0 | 1356 | 2 | 0 | 0 | 2 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | ACTTC others(1351): Show |
chr13 | 49490953 | 49533976 |
| a0002c0003t0001 | 0/0 | 1335 | 5 | 5 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | ACTTC others(1330): Show |
chr13 | 49490953 | 49533976 |
| a0003c0006t0001 | 0/0 | 1356 | 2 | 2 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | ACTTC others(1351): Show |
chr13 | 49490953 | 49533976 |
| a0004c0007t0001 | 0/0 | 1356 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | ACTTC others(1351): Show |
chr13 | 49490953 | 49533976 |
| a0005c0008t0001 | 0/0 | 1356 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | ACTTC others(1351): Show |
chr13 | 49490953 | 49533976 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 7 | 0 | 4 | 3 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0001g0006 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0001g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0001g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0001g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0001g0024 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0001g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0001g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0002g0001 | 0/0 | 19 | 0 | 2 | 14 | 0 | 3 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0002g0005 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0002g0007 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0002g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0002g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0002g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0002g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0002g0023 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0002g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0002g0026 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0002g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0002g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0002g0029 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0002g0030 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0002g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0002g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0002g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0002g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0002g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0002g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0002g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0002g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0002g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0002g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0002g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0002g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0002g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0002g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0002g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0002g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0002g0198 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0002g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0002g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0002g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0002g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0002g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0002g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0002g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0002g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0002g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0002g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0002g0330 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0002g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0002g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0003g0004 | 0/0 | 4 | 0 | 0 | 3 | 1 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0003g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0003g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0003g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0003g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0003g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0003g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0003g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0003g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0003g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0003g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0003g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0003g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0003g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0003g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0003g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0003g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0003g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0003g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0003g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0003g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0003g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0003g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0003g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0003g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0003g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0003g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0003g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0003g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0003g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0003g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0003g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0003g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0003g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0003g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0003g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0003g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0003g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0003g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0003g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0003g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0003g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0003g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0001t0004g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0002t0001g0002 | 0/0 | 9 | 0 | 4 | 2 | 1 | 2 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0002t0001g0011 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0002t0001g0013 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0002t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0002t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0002t0001g0020 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0002t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0002t0001g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0002t0001g0040 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0002t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0002t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0002t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0002t0001g0078 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0002t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0002t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0002t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0002t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0002t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0002t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0002t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0002t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0002t0001g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0002t0001g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0002t0001g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0002t0001g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0002t0001g0327 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0002t0001g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0002t0001g0329 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0002t0002g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0002t0002g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0002t0002g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0002t0002g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0002t0002g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0004t0002g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0005t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0001c0005t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0002c0003t0001g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0002c0003t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0002c0003t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0002c0003t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0003c0006t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0003c0006t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0004c0007t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| a0005c0008t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0128 | EUR | GBR | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0173 | EUR | GBR | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG00140 | hp1 | a0001 | c0002 | t0001 | g0071 | EUR | GBR | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0171 | EUR | GBR | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG00280 | hp1 | a0001 | c0002 | t0001 | g0327 | EUR | FIN | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0210 | EUR | FIN | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0294 | EAS | CHS | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0264 | EAS | CHS | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0222 | EAS | CHS | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | CHS | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0228 | EAS | CHS | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | CHS | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG00558 | hp1 | a0001 | c0001 | t0003 | g0248 | EAS | CHS | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG00558 | hp2 | a0001 | c0001 | t0003 | g0258 | EAS | CHS | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0320 | EAS | CHS | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0177 | EAS | CHS | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG00609 | hp2 | a0001 | c0002 | t0001 | g0081 | EAS | CHS | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | CHS | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0030 | AMR | PUR | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG00639 | hp2 | a0001 | c0002 | t0001 | g0040 | AMR | PUR | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0305 | AMR | PUR | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG00642 | hp2 | a0001 | c0001 | t0003 | g0263 | AMR | PUR | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0114 | EAS | CHS | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0149 | AMR | PUR | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG00733 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG00735 | hp1 | a0001 | c0002 | t0001 | g0105 | AMR | PUR | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0205 | AMR | PUR | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0179 | AMR | PUR | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG00741 | hp2 | a0001 | c0002 | t0002 | g0316 | AMR | PUR | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG01069 | hp1 | a0001 | c0004 | t0002 | g0009 | AMR | PUR | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG01069 | hp2 | a0001 | c0002 | t0001 | g0013 | AMR | PUR | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG01070 | hp2 | a0001 | c0002 | t0001 | g0089 | AMR | PUR | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG01071 | hp1 | a0001 | c0004 | t0002 | g0009 | AMR | PUR | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG01071 | hp2 | a0001 | c0002 | t0001 | g0084 | AMR | PUR | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0142 | AMR | PUR | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG01074 | hp2 | a0001 | c0002 | t0001 | g0039 | AMR | PUR | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG01081 | hp1 | a0001 | c0002 | t0001 | g0324 | AMR | PUR | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG01099 | hp1 | a0001 | c0002 | t0001 | g0061 | AMR | PUR | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0166 | AMR | PUR | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0023 | AMR | PUR | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG01106 | hp2 | a0001 | c0002 | t0001 | g0106 | AMR | PUR | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0070 | AMR | PUR | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG01168 | hp1 | a0001 | c0002 | t0001 | g0315 | AMR | PUR | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0163 | AMR | PUR | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0153 | AMR | PUR | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0321 | AMR | PUR | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0243 | AMR | PUR | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG01255 | hp2 | a0001 | c0001 | t0003 | g0185 | AMR | CLM | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG01256 | hp2 | a0001 | c0002 | t0001 | g0317 | AMR | CLM | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0147 | AMR | CLM | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | CLM | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG01258 | hp1 | a0001 | c0002 | t0001 | g0039 | AMR | CLM | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0146 | AMR | CLM | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0172 | AMR | CLM | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0159 | AMR | CLM | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG01358 | hp1 | a0001 | c0002 | t0001 | g0325 | AMR | CLM | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0189 | AMR | CLM | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0155 | AMR | CLM | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0322 | AMR | CLM | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG01496 | hp1 | a0001 | c0001 | t0003 | g0184 | AMR | CLM | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0161 | AMR | CLM | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG01516 | hp1 | a0001 | c0002 | t0001 | g0329 | EUR | IBS | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG01516 | hp2 | a0001 | c0002 | t0001 | g0002 | EUR | IBS | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG01517 | hp1 | a0001 | c0002 | t0001 | g0013 | EUR | IBS | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0330 | EUR | IBS | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0242 | AFR | ACB | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0226 | AFR | ACB | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0240 | AFR | ACB | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0225 | AFR | ACB | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG01928 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PEL | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0029 | AMR | PEL | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG01934 | hp1 | a0001 | c0002 | t0001 | g0085 | AMR | PEL | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0201 | AMR | PEL | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG01943 | hp1 | a0001 | c0002 | t0002 | g0091 | AMR | PEL | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0188 | AMR | PEL | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0314 | AMR | PEL | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG01952 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | PEL | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0026 | AMR | PEL | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG01975 | hp2 | a0001 | c0002 | t0002 | g0086 | AMR | PEL | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PEL | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG01978 | hp2 | a0001 | c0002 | t0001 | g0094 | AMR | PEL | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PEL | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0332 | AMR | PEL | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG01993 | hp1 | a0001 | c0002 | t0002 | g0326 | AMR | PEL | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG01993 | hp2 | a0001 | c0002 | t0001 | g0060 | AMR | PEL | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | PEL | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG02015 | hp1 | a0001 | c0001 | t0003 | g0276 | EAS | KHV | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | KHV | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | KHV | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG02027 | hp2 | a0001 | c0001 | t0003 | g0269 | EAS | KHV | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG02040 | hp1 | a0001 | c0002 | t0001 | g0021 | EAS | KHV | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0199 | AFR | ACB | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0148 | AFR | ACB | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG02056 | hp1 | a0001 | c0002 | t0001 | g0101 | EAS | KHV | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG02056 | hp2 | a0001 | c0001 | t0003 | g0037 | EAS | KHV | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0306 | EAS | KHV | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0219 | EAS | KHV | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | KHV | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0285 | EAS | KHV | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG02083 | hp2 | a0001 | c0002 | t0001 | g0019 | EAS | KHV | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | KHV | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG02132 | hp2 | a0001 | c0001 | t0003 | g0261 | EAS | KHV | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | KHV | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG02135 | hp2 | a0001 | c0001 | t0003 | g0037 | EAS | KHV | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG02145 | hp1 | a0002 | c0003 | t0001 | g0041 | AFR | ACB | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0236 | AFR | ACB | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG02148 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PEL | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | PEL | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0318 | EAS | CDX | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG02155 | hp2 | a0001 | c0001 | t0003 | g0273 | EAS | CDX | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | CDX | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG02165 | hp2 | a0001 | c0002 | t0001 | g0082 | EAS | CDX | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | ACB | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0137 | AFR | ACB | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0244 | AFR | ACB | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0145 | AFR | ACB | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0323 | AMR | PEL | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG02273 | hp2 | a0001 | c0002 | t0001 | g0077 | AMR | PEL | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0025 | AFR | ACB | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | ACB | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0194 | AMR | PEL | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0295 | AMR | PEL | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | ACB | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0031 | EAS | KHV | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG02572 | hp1 | a0001 | c0002 | t0002 | g0283 | AFR | GWD | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG02572 | hp2 | a0004 | c0007 | t0001 | g0064 | AFR | GWD | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG02602 | hp1 | a0001 | c0001 | t0003 | g0279 | SAS | PJL | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0046 | SAS | PJL | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG02615 | hp1 | a0001 | c0002 | t0001 | g0282 | AFR | GWD | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG02615 | hp2 | a0001 | c0002 | t0001 | g0011 | AFR | GWD | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0007 | AFR | GWD | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0245 | AFR | GWD | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0132 | AFR | GWD | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0025 | AFR | GWD | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | GWD | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0026 | AFR | GWD | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG02698 | hp1 | a0001 | c0001 | t0003 | g0268 | SAS | PJL | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0051 | SAS | PJL | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG02717 | hp1 | a0003 | c0006 | t0001 | g0067 | AFR | GWD | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0144 | AFR | GWD | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0100 | SAS | PJL | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0162 | SAS | PJL | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | GWD | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0238 | AFR | GWD | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0241 | AFR | GWD | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | GWD | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | GWD | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | GWD | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG02896 | hp1 | a0001 | c0002 | t0001 | g0011 | AFR | GWD | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | GWD | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0247 | AFR | GWD | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | GWD | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | ESN | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | ESN | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0234 | AFR | ESN | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | ESN | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0333 | AFR | ESN | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG03017 | hp1 | a0001 | c0001 | t0003 | g0256 | SAS | PJL | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG03017 | hp2 | a0001 | c0002 | t0001 | g0102 | SAS | PJL | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG03041 | hp1 | a0002 | c0003 | t0001 | g0017 | AFR | GWD | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | GWD | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0130 | AFR | MSL | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0239 | AFR | MSL | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | ESN | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0202 | AFR | ESN | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG03139 | hp1 | a0003 | c0006 | t0001 | g0066 | AFR | ESN | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0023 | AFR | ESN | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0007 | AFR | ESN | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0129 | AFR | ESN | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0108 | AFR | MSL | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0022 | AFR | MSL | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | MSL | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0203 | AFR | MSL | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG03239 | hp1 | a0001 | c0002 | t0001 | g0002 | SAS | PJL | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0207 | SAS | PJL | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | MSL | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | MSL | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0134 | AFR | MSL | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | MSL | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0117 | SAS | PJL | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG03491 | hp1 | a0001 | c0002 | t0001 | g0079 | SAS | PJL | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG03491 | hp2 | a0001 | c0002 | t0001 | g0095 | SAS | PJL | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG03492 | hp2 | a0001 | c0002 | t0001 | g0096 | SAS | PJL | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | ESN | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0187 | AFR | ESN | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0009 | AFR | GWD | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0183 | AFR | GWD | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0107 | AFR | MSL | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0224 | AFR | MSL | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG03654 | hp1 | a0001 | c0001 | t0003 | g0278 | SAS | PJL | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0250 | SAS | PJL | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0331 | SAS | PJL | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0120 | SAS | PJL | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG03688 | hp1 | a0001 | c0001 | t0003 | g0271 | SAS | STU | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0178 | SAS | STU | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0176 | SAS | PJL | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG03710 | hp1 | a0001 | c0002 | t0001 | g0020 | SAS | PJL | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0193 | SAS | BEB | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG03834 | hp2 | a0001 | c0002 | t0001 | g0088 | SAS | BEB | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG03927 | hp1 | a0001 | c0002 | t0001 | g0098 | SAS | BEB | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0195 | SAS | BEB | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0055 | SAS | BEB | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG03942 | hp2 | a0001 | c0002 | t0001 | g0002 | SAS | BEB | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0206 | SAS | BEB | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0167 | SAS | BEB | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0047 | SAS | STU | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0156 | SAS | STU | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG04204 | hp1 | a0001 | c0001 | t0003 | g0311 | SAS | STU | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | STU | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0204 | SAS | STU | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0123 | SAS | STU | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | YRI | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | YRI | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0038 | EAS | CHB | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA18612 | hp2 | a0001 | c0001 | t0003 | g0267 | EAS | CHB | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0298 | EAS | CHB | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHB | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0151 | AFR | YRI | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0022 | AFR | YRI | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0180 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA18939 | hp2 | a0001 | c0001 | t0003 | g0265 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA18940 | hp1 | a0001 | c0001 | t0002 | g0169 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA18940 | hp2 | a0001 | c0001 | t0003 | g0262 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA18942 | hp2 | a0001 | c0001 | t0003 | g0254 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA18943 | hp1 | a0001 | c0002 | t0001 | g0018 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA18943 | hp2 | a0001 | c0001 | t0003 | g0255 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA18944 | hp2 | a0001 | c0001 | t0003 | g0186 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA18945 | hp2 | a0001 | c0001 | t0003 | g0260 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0297 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0216 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA18947 | hp2 | a0001 | c0002 | t0001 | g0020 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0227 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA18948 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA18950 | hp2 | a0001 | c0002 | t0001 | g0093 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA18952 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0290 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0165 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0221 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA18959 | hp2 | a0001 | c0001 | t0003 | g0266 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA18961 | hp1 | a0001 | c0002 | t0001 | g0074 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0215 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA18963 | hp1 | a0001 | c0001 | t0002 | g0217 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0197 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA18964 | hp2 | a0001 | c0002 | t0001 | g0083 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0168 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA18966 | hp1 | a0001 | c0005 | t0002 | g0157 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA18966 | hp2 | a0001 | c0002 | t0001 | g0076 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0160 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA18971 | hp1 | a0005 | c0008 | t0001 | g0303 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA18973 | hp1 | a0001 | c0001 | t0003 | g0035 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA18974 | hp1 | a0001 | c0001 | t0003 | g0257 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0212 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA18977 | hp2 | a0001 | c0001 | t0003 | g0253 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0302 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0164 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA18980 | hp2 | a0001 | c0002 | t0001 | g0019 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA18981 | hp2 | a0001 | c0002 | t0001 | g0103 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0296 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0230 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA18983 | hp2 | a0001 | c0001 | t0003 | g0035 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA18984 | hp1 | a0001 | c0002 | t0001 | g0090 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA18985 | hp1 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA18985 | hp2 | a0001 | c0001 | t0003 | g0259 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA18986 | hp1 | a0001 | c0002 | t0001 | g0021 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA18987 | hp1 | a0001 | c0001 | t0002 | g0174 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA18987 | hp2 | a0001 | c0001 | t0002 | g0288 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA18989 | hp1 | a0001 | c0001 | t0003 | g0284 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA18991 | hp2 | a0001 | c0001 | t0002 | g0218 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA18994 | hp1 | a0001 | c0002 | t0001 | g0097 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA18997 | hp1 | a0001 | c0001 | t0002 | g0287 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA18997 | hp2 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0289 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA18998 | hp2 | a0001 | c0001 | t0003 | g0280 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA19000 | hp1 | a0001 | c0001 | t0003 | g0277 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0275 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA19001 | hp1 | a0001 | c0001 | t0002 | g0235 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0220 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA19003 | hp2 | a0001 | c0001 | t0003 | g0036 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA19004 | hp1 | a0001 | c0002 | t0001 | g0073 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA19006 | hp1 | a0001 | c0002 | t0001 | g0092 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA19006 | hp2 | a0001 | c0001 | t0002 | g0319 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0301 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA19007 | hp2 | a0001 | c0001 | t0003 | g0312 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0190 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA19009 | hp2 | a0001 | c0001 | t0003 | g0274 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0150 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA19010 | hp2 | a0001 | c0002 | t0001 | g0099 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0223 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0136 | AFR | LWK | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA19030 | hp2 | a0002 | c0003 | t0001 | g0063 | AFR | LWK | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA19055 | hp1 | a0001 | c0001 | t0002 | g0300 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA19055 | hp2 | a0001 | c0002 | t0001 | g0075 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA19057 | hp2 | a0001 | c0001 | t0003 | g0313 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA19060 | hp1 | a0001 | c0001 | t0003 | g0251 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0211 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA19062 | hp2 | a0001 | c0001 | t0003 | g0252 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA19064 | hp2 | a0001 | c0001 | t0003 | g0036 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA19065 | hp2 | a0001 | c0002 | t0001 | g0080 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA19066 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA19068 | hp1 | a0001 | c0001 | t0003 | g0310 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0304 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA19078 | hp1 | a0001 | c0001 | t0003 | g0309 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA19078 | hp2 | a0001 | c0001 | t0002 | g0152 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0308 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA19085 | hp2 | a0001 | c0002 | t0001 | g0018 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA19086 | hp1 | a0001 | c0005 | t0002 | g0175 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA19086 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0229 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA19088 | hp2 | a0001 | c0001 | t0003 | g0281 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA19089 | hp1 | a0001 | c0001 | t0002 | g0209 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA19089 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA19090 | hp1 | a0001 | c0001 | t0003 | g0270 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0291 | EAS | JPT | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA19240 | hp1 | a0001 | c0001 | t0004 | g0237 | AFR | YRI | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | YRI | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | ASW | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0286 | AFR | ASW | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0030 | EUR | TSI | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA20752 | hp2 | a0001 | c0001 | t0003 | g0004 | EUR | TSI | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0170 | EUR | TSI | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA20805 | hp2 | a0001 | c0002 | t0001 | g0013 | EUR | TSI | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0299 | SAS | GIH | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA20905 | hp2 | a0001 | c0002 | t0001 | g0087 | SAS | GIH | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0192 | AMR | CLM | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG01123 | hp2 | a0001 | c0002 | t0001 | g0328 | AMR | CLM | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0246 | AFR | ACB | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG02109 | hp2 | a0002 | c0003 | t0001 | g0065 | AFR | ACB | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0135 | AFR | ACB | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0200 | AFR | ACB | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0131 | AFR | ACB | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG02559 | hp2 | a0001 | c0002 | t0001 | g0040 | AFR | ACB | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG03471 | hp1 | a0001 | c0002 | t0001 | g0011 | AFR | MSL | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | MSL | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG06807 | hp1 | a0001 | c0002 | t0001 | g0104 | AFR | USA | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | USA | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0007 | AFR | USA | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | USA | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA21309 | hp1 | a0002 | c0003 | t0001 | g0017 | AFR | LWK | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| NA21309 | hp2 | a0001 | c0001 | t0003 | g0272 | AFR | LWK | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0198 | REF | REF | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0001 | g0078 | REF | REF | PHF11_chr13_49490953_49533976 | PHF11 | chr13 | 49490953 | 49533976 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:49496005 | GCCCAGGC others(14): Show |
G | 1 | a0002 | 5 | HG02109.hp2 HG02145.hp1 HG03041.hp1 others(2): Show |
conservative_inframe_deletion | MODERATE | c.7_27delCAGGCGTCGCC others(10): Show |
p.Gln3_Pro9del | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/10 | 56/1356 | 7/996 | 3/331 | INFO_REALIGN_3_PRIME | chr13 | 49496005 | ||
| chr13:49496062 | C | G | 1 | a0003 | 2 | HG02717.hp1 HG03139.hp1 |
missense_variant | MODERATE | c.61C>G | p.Arg21Gly | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/10 | 110/1356 | 61/996 | 21/331 | chr13 | 49496062 | |||
| chr13:49496071 | C | G | 1 | a0005 | 1 | NA18971.hp1 | missense_variant | MODERATE | c.70C>G | p.Gln24Glu | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/10 | 119/1356 | 70/996 | 24/331 | chr13 | 49496071 | |||
| chr13:49528658 | C | A | 2 | a0002 a0004 |
6 | HG02109.hp2 HG02145.hp1 HG02572.hp2 others(3): Show |
missense_variant | MODERATE | c.989C>A | p.Ser330Tyr | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 10/10 | 1038/1356 | 989/996 | 330/331 | chr13 | 49528658 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:49506711 | A | G | 7 | a0001c0001 a0001c0004 a0001c0005 others(4): Show |
339 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(336): Show |
synonymous_variant | LOW | c.171A>G | p.Leu57Leu | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/10 | 220/1356 | 171/996 | 57/331 | chr13 | 49506711 | |||
| chr13:49518110 | C | T | 1 | a0001c0005 | 2 | NA18966.hp1 NA19086.hp1 |
synonymous_variant | LOW | c.417C>T | p.Asp139Asp | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 4/10 | 466/1356 | 417/996 | 139/331 | chr13 | 49518110 | |||
| chr13:49518113 | C | T | 1 | a0001c0004 | 2 | HG01069.hp1 HG01071.hp1 |
synonymous_variant | LOW | c.420C>T | p.Asp140Asp | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 4/10 | 469/1356 | 420/996 | 140/331 | chr13 | 49518113 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:49495984 | C | T | 1 | a0001c0001t0004 | 1 | NA19240.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-18C>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/10 | chr13 | 49495984 | |||||||
| chr13:49528674 | G | A | 4 | a0001c0001t0002 a0001c0002t0002 a0001c0004t0002 others(1): Show |
178 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(175): Show |
3_prime_UTR_variant | MODIFIER | c.*9G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 10/10 | 9 | chr13 | 49528674 | ||||||
| chr13:49528856 | T | C | 4 | a0001c0001t0002 a0001c0002t0002 a0001c0004t0002 others(1): Show |
178 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(175): Show |
3_prime_UTR_variant | MODIFIER | c.*191T>C | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 10/10 | 191 | chr13 | 49528856 | ||||||
| chr13:49528946 | C | CTCT | 1 | a0001c0001t0003 | 49 | HG00558.hp1 HG00558.hp2 HG00642.hp2 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*283_*285dupCTT | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 10/10 | 286 | INFO_REALIGN_3_PRIME | chr13 | 49528946 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:49496108 | GGGGC | G | 248 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0024 others(245): Show |
308 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(305): Show |
intron_variant | MODIFIER | c.94+33_94+36delCGGG | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 49496108 | ||||||
| chr13:49496108 | GGGGCGGG others(9): Show |
G | 1 | a0001c0001t0001g0333 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.94+21_94+36delCGGG others(12): Show |
PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 49496108 | ||||||
| chr13:49496147 | G | T | 3 | a0001c0001t0002g0330 a0001c0001t0002g0331 a0001c0001t0002g0332 |
3 | HG01517.hp2 HG01981.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.94+52G>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49496147 | |||||||
| chr13:49496280 | G | A | 1 | a0002c0003t0001g0041 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.94+185G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49496280 | |||||||
| chr13:49496286 | G | A | 1 | a0001c0001t0002g0114 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.94+191G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49496286 | |||||||
| chr13:49496390 | A | G | 1 | a0001c0001t0001g0113 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.94+295A>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49496390 | |||||||
| chr13:49496465 | G | A | 1 | a0001c0001t0002g0022 | 2 | HG03209.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.94+370G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49496465 | |||||||
| chr13:49496470 | G | A | 1 | a0001c0001t0001g0042 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.94+375G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49496470 | |||||||
| chr13:49496509 | A | G | 1 | a0001c0001t0001g0112 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.94+414A>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49496509 | |||||||
| chr13:49496612 | G | C | 4 | a0001c0001t0001g0014 a0001c0001t0001g0043 a0001c0001t0001g0044 others(1): Show |
5 | HG02818.hp1 HG02922.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.94+517G>C | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49496612 | |||||||
| chr13:49496830 | C | CT | 121 | a0001c0001t0001g0024 a0001c0001t0001g0113 a0001c0001t0001g0133 others(118): Show |
153 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.94+756dupT | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 49496830 | ||||||
| chr13:49496830 | C | CTT | 13 | a0001c0001t0001g0045 a0001c0001t0001g0224 a0001c0001t0001g0225 others(10): Show |
13 | HG00544.hp1 HG00544.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.94+755_94+756dupTT | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 49496830 | ||||||
| chr13:49496830 | C | CTTT | 16 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0236 others(13): Show |
18 | HG00558.hp1 HG01243.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.94+754_94+756dupTT others(1): Show |
PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 49496830 | ||||||
| chr13:49496830 | C | CTTTT | 36 | a0001c0001t0001g0109 a0001c0001t0001g0250 a0001c0001t0002g0264 others(33): Show |
41 | HG00408.hp2 HG00558.hp2 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.94+753_94+756dupTT others(2): Show |
PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 49496830 | ||||||
| chr13:49496830 | C | CTTTTT | 42 | a0001c0001t0001g0003 a0001c0001t0001g0042 a0001c0001t0001g0110 others(39): Show |
57 | HG00408.hp1 HG00642.hp1 HG01081.hp2 others(54): Show |
intron_variant | MODIFIER | c.94+752_94+756dupTT others(3): Show |
PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 49496830 | ||||||
| chr13:49496830 | C | CTTTTTT | 11 | a0001c0001t0001g0320 a0001c0001t0001g0321 a0001c0001t0001g0322 others(8): Show |
13 | HG00597.hp2 HG00639.hp2 HG00741.hp2 others(10): Show |
intron_variant | MODIFIER | c.94+751_94+756dupTT others(4): Show |
PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 49496830 | ||||||
| chr13:49496830 | C | CTTTTTTT | 7 | a0001c0002t0001g0013 a0001c0002t0001g0324 a0001c0002t0001g0325 others(4): Show |
9 | HG00280.hp1 HG01069.hp2 HG01081.hp1 others(6): Show |
intron_variant | MODIFIER | c.94+750_94+756dupTT others(5): Show |
PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 49496830 | ||||||
| chr13:49496830 | CT | C | 22 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0015 others(19): Show |
27 | HG01109.hp1 HG01257.hp2 HG01993.hp2 others(24): Show |
intron_variant | MODIFIER | c.94+756delT | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 49496830 | ||||||
| chr13:49496926 | C | T | 108 | a0001c0001t0001g0045 a0001c0001t0001g0154 a0001c0001t0001g0158 others(105): Show |
137 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(134): Show |
intron_variant | MODIFIER | c.94+831C>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49496926 | |||||||
| chr13:49496973 | A | G | 14 | a0001c0001t0002g0211 a0001c0001t0002g0212 a0001c0001t0002g0213 others(11): Show |
14 | HG00438.hp1 HG02074.hp1 NA18946.hp2 others(11): Show |
intron_variant | MODIFIER | c.94+878A>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49496973 | |||||||
| chr13:49497218 | G | A | 1 | a0001c0001t0001g0046 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.94+1123G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49497218 | |||||||
| chr13:49497571 | T | C | 253 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0024 others(250): Show |
313 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(310): Show |
intron_variant | MODIFIER | c.94+1476T>C | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49497571 | |||||||
| chr13:49497801 | T | C | 1 | a0001c0001t0001g0113 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.94+1706T>C | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49497801 | |||||||
| chr13:49498109 | A | G | 18 | a0001c0001t0002g0031 a0001c0001t0002g0032 a0001c0001t0002g0114 others(15): Show |
20 | HG00099.hp1 HG00280.hp2 HG00673.hp1 others(17): Show |
intron_variant | MODIFIER | c.94+2014A>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49498109 | |||||||
| chr13:49498273 | C | A | 1 | a0001c0001t0002g0201 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.94+2178C>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49498273 | |||||||
| chr13:49498293 | T | C | 16 | a0001c0002t0001g0011 a0001c0002t0001g0013 a0001c0002t0001g0039 others(13): Show |
22 | HG00280.hp1 HG00639.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.94+2198T>C | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49498293 | |||||||
| chr13:49498386 | AATCATTC others(63): Show |
A | 36 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0015 others(33): Show |
44 | HG01109.hp1 HG01109.hp2 HG01257.hp2 others(41): Show |
intron_variant | MODIFIER | c.94+2321_94+2390del others(70): Show |
PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 49498386 | ||||||
| chr13:49498491 | G | T | 15 | a0001c0001t0001g0008 a0001c0001t0001g0115 a0001c0001t0001g0116 others(12): Show |
17 | HG00621.hp1 HG02165.hp1 HG03490.hp2 others(14): Show |
intron_variant | MODIFIER | c.94+2396G>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49498491 | |||||||
| chr13:49498495 | A | G | 3 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0070 |
3 | HG01109.hp2 HG02895.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.94+2400A>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49498495 | |||||||
| chr13:49498735 | A | T | 2 | a0001c0001t0001g0112 a0001c0001t0001g0333 |
2 | HG02647.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.94+2640A>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49498735 | |||||||
| chr13:49498839 | T | C | 2 | a0001c0001t0003g0037 a0001c0001t0003g0284 |
3 | HG02056.hp2 HG02135.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.94+2744T>C | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49498839 | |||||||
| chr13:49498870 | A | T | 3 | a0001c0001t0002g0005 a0001c0001t0002g0314 a0001c0001t0002g0323 |
6 | HG01952.hp1 HG01978.hp1 HG01981.hp1 others(3): Show |
intron_variant | MODIFIER | c.94+2775A>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49498870 | |||||||
| chr13:49499223 | T | G | 7 | a0001c0001t0002g0025 a0001c0001t0002g0026 a0001c0001t0002g0144 others(4): Show |
9 | HG01257.hp1 HG01258.hp2 HG01975.hp1 others(6): Show |
intron_variant | MODIFIER | c.94+3128T>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49499223 | |||||||
| chr13:49499282 | G | A | 4 | a0001c0001t0001g0042 a0001c0001t0001g0109 a0001c0001t0001g0110 others(1): Show |
4 | HG02895.hp2 HG02897.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.94+3187G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49499282 | |||||||
| chr13:49499343 | C | T | 1 | a0001c0001t0001g0113 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.94+3248C>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49499343 | |||||||
| chr13:49499427 | C | G | 253 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0024 others(250): Show |
313 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(310): Show |
intron_variant | MODIFIER | c.94+3332C>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49499427 | |||||||
| chr13:49499467 | T | C | 1 | a0001c0001t0001g0224 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.94+3372T>C | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49499467 | |||||||
| chr13:49499633 | G | A | 1 | a0001c0001t0001g0236 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.94+3538G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49499633 | |||||||
| chr13:49499933 | C | A | 1 | a0001c0001t0002g0211 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.94+3838C>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49499933 | |||||||
| chr13:49499968 | G | A | 5 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0070 others(2): Show |
5 | HG01109.hp2 HG02647.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.94+3873G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49499968 | |||||||
| chr13:49500014 | G | A | 1 | a0001c0001t0001g0062 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.94+3919G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49500014 | |||||||
| chr13:49500521 | G | A | 4 | a0001c0001t0001g0033 a0001c0001t0001g0238 a0001c0001t0001g0239 others(1): Show |
5 | HG02451.hp1 HG02818.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.94+4426G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49500521 | |||||||
| chr13:49500546 | C | T | 2 | a0001c0001t0001g0100 a0001c0002t0001g0101 |
2 | HG02056.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.94+4451C>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49500546 | |||||||
| chr13:49500616 | A | G | 275 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(272): Show |
337 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(334): Show |
intron_variant | MODIFIER | c.94+4521A>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49500616 | |||||||
| chr13:49500620 | A | C | 258 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(255): Show |
318 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(315): Show |
intron_variant | MODIFIER | c.94+4525A>C | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49500620 | |||||||
| chr13:49500726 | ACAG | A | 3 | a0001c0001t0002g0128 a0001c0001t0002g0201 a0001c0001t0002g0210 |
3 | HG00099.hp1 HG00280.hp2 HG01934.hp2 |
intron_variant | MODIFIER | c.94+4635_94+4637del others(3): Show |
PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 49500726 | ||||||
| chr13:49500782 | G | A | 2 | a0001c0001t0002g0107 a0001c0001t0002g0108 |
2 | HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.94+4687G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49500782 | |||||||
| chr13:49500914 | C | T | 3 | a0001c0001t0002g0030 a0001c0001t0002g0199 a0001c0001t0002g0200 |
4 | HG00639.hp1 HG02055.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.94+4819C>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49500914 | |||||||
| chr13:49500971 | C | T | 6 | a0001c0001t0001g0024 a0001c0001t0001g0138 a0001c0001t0001g0139 others(3): Show |
7 | HG01074.hp1 HG01243.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.94+4876C>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49500971 | |||||||
| chr13:49500995 | C | CT | 3 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0333 |
3 | HG01109.hp2 HG02976.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.94+4904dupT | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 49500995 | ||||||
| chr13:49501000 | G | GT | 30 | a0001c0001t0001g0126 a0001c0001t0001g0127 a0001c0001t0001g0286 others(27): Show |
33 | HG01123.hp1 HG01358.hp2 HG01516.hp1 others(30): Show |
intron_variant | MODIFIER | c.94+4920dupT | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 49501000 | ||||||
| chr13:49501000 | G | GTT | 29 | a0001c0001t0001g0003 a0001c0001t0001g0109 a0001c0001t0001g0110 others(26): Show |
38 | HG00408.hp1 HG00544.hp2 HG00558.hp1 others(35): Show |
intron_variant | MODIFIER | c.94+4919_94+4920dup others(2): Show |
PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 49501000 | ||||||
| chr13:49501000 | G | GTTT | 15 | a0001c0001t0001g0042 a0001c0001t0001g0305 a0001c0001t0001g0306 others(12): Show |
18 | HG00597.hp2 HG00642.hp1 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.94+4918_94+4920dup others(3): Show |
PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 49501000 | ||||||
| chr13:49501000 | G | GTTTT | 7 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0140 others(4): Show |
7 | HG01074.hp1 HG01433.hp2 HG01952.hp1 others(4): Show |
intron_variant | MODIFIER | c.94+4917_94+4920dup others(4): Show |
PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 49501000 | ||||||
| chr13:49501000 | G | T | 60 | a0001c0001t0001g0014 a0001c0001t0001g0033 a0001c0001t0001g0034 others(57): Show |
69 | HG00408.hp2 HG00558.hp2 HG00642.hp2 others(66): Show |
intron_variant | MODIFIER | c.94+4905G>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49501000 | |||||||
| chr13:49501001 | TTTTTTTT others(9): Show |
T | 1 | a0001c0001t0001g0143 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.94+4918_94+4933del others(16): Show |
PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 49501001 | ||||||
| chr13:49501003 | T | G | 6 | a0001c0002t0001g0002 a0001c0002t0001g0060 a0001c0002t0001g0077 others(3): Show |
7 | HG00733.hp2 HG01934.hp1 HG01943.hp1 others(4): Show |
intron_variant | MODIFIER | c.94+4908T>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49501003 | |||||||
| chr13:49501006 | T | G | 25 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0016 others(22): Show |
30 | HG01109.hp1 HG01257.hp2 HG02015.hp2 others(27): Show |
intron_variant | MODIFIER | c.94+4911T>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49501006 | |||||||
| chr13:49501007 | T | G | 1 | a0001c0001t0001g0015 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.94+4912T>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49501007 | |||||||
| chr13:49501010 | TTTTTTGG | T | 17 | a0001c0001t0001g0014 a0001c0001t0001g0033 a0001c0001t0001g0034 others(14): Show |
20 | HG01243.hp2 HG01884.hp1 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.94+4921_94+4927del others(7): Show |
PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 49501010 | ||||||
| chr13:49501011 | T | G | 1 | a0001c0001t0002g0007 | 2 | HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.94+4916T>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49501011 | |||||||
| chr13:49501011 | TTTTTGG | T | 31 | a0001c0001t0002g0275 a0001c0001t0003g0004 a0001c0001t0003g0035 others(28): Show |
37 | HG00558.hp2 HG00642.hp2 HG02015.hp1 others(34): Show |
intron_variant | MODIFIER | c.94+4921_94+4926del others(6): Show |
PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 49501011 | ||||||
| chr13:49501012 | T | G | 2 | a0001c0002t0001g0002 a0001c0002t0001g0096 |
2 | HG02148.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.94+4917T>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49501012 | |||||||
| chr13:49501012 | TTTTGG | T | 31 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0016 others(28): Show |
36 | HG00408.hp2 HG01109.hp1 HG01257.hp2 others(33): Show |
intron_variant | MODIFIER | c.94+4921_94+4925del others(5): Show |
PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 49501012 | ||||||
| chr13:49501013 | T | G | 1 | a0001c0001t0001g0241 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.94+4918T>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49501013 | |||||||
| chr13:49501015 | TG | T | 12 | a0001c0001t0001g0117 a0001c0001t0001g0133 a0001c0001t0001g0225 others(9): Show |
14 | HG01106.hp1 HG01891.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.94+4922delG | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 49501015 | ||||||
| chr13:49501016 | G | T | 179 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0024 others(176): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(221): Show |
intron_variant | MODIFIER | c.94+4921G>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49501016 | |||||||
| chr13:49501017 | G | T | 244 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0024 others(241): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.94+4922G>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49501017 | |||||||
| chr13:49501021 | T | G | 1 | a0001c0002t0001g0071 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.94+4926T>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49501021 | |||||||
| chr13:49501052 | C | T | 1 | a0001c0001t0002g0114 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.94+4957C>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49501052 | |||||||
| chr13:49501058 | G | C | 2 | a0003c0006t0001g0066 a0003c0006t0001g0067 |
2 | HG02717.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.94+4963G>C | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49501058 | |||||||
| chr13:49501076 | C | T | 3 | a0001c0001t0002g0107 a0001c0001t0002g0108 a0001c0001t0002g0137 |
3 | HG02257.hp2 HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.94+4981C>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49501076 | |||||||
| chr13:49501087 | C | G | 5 | a0001c0002t0001g0013 a0001c0002t0001g0061 a0001c0002t0001g0327 others(2): Show |
7 | HG00280.hp1 HG01069.hp2 HG01099.hp1 others(4): Show |
intron_variant | MODIFIER | c.94+4992C>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49501087 | |||||||
| chr13:49501090 | C | T | 15 | a0001c0001t0001g0008 a0001c0001t0001g0115 a0001c0001t0001g0116 others(12): Show |
17 | HG00621.hp1 HG02165.hp1 HG03490.hp2 others(14): Show |
intron_variant | MODIFIER | c.94+4995C>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49501090 | |||||||
| chr13:49501240 | C | T | 1 | a0001c0001t0002g0108 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.94+5145C>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49501240 | |||||||
| chr13:49501245 | T | A | 1 | a0001c0001t0001g0072 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.94+5150T>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49501245 | |||||||
| chr13:49501304 | C | T | 9 | a0001c0001t0001g0024 a0001c0001t0001g0138 a0001c0001t0001g0139 others(6): Show |
11 | HG01074.hp1 HG01243.hp1 HG02922.hp1 others(8): Show |
intron_variant | MODIFIER | c.94+5209C>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49501304 | |||||||
| chr13:49501382 | A | G | 1 | a0001c0001t0003g0279 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.95-5253A>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49501382 | |||||||
| chr13:49501730 | G | A | 1 | a0001c0001t0001g0072 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.95-4905G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49501730 | |||||||
| chr13:49501793 | T | C | 277 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(274): Show |
339 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(336): Show |
intron_variant | MODIFIER | c.95-4842T>C | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49501793 | |||||||
| chr13:49501938 | G | A | 14 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0046 others(11): Show |
17 | HG01257.hp2 HG02015.hp2 HG02083.hp1 others(14): Show |
intron_variant | MODIFIER | c.95-4697G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49501938 | |||||||
| chr13:49501943 | G | A | 99 | a0001c0001t0001g0154 a0001c0001t0001g0158 a0001c0001t0001g0224 others(96): Show |
128 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(125): Show |
intron_variant | MODIFIER | c.95-4692G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49501943 | |||||||
| chr13:49501981 | G | A | 1 | a0001c0001t0001g0072 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.95-4654G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49501981 | |||||||
| chr13:49502037 | T | C | 4 | a0001c0001t0002g0012 a0001c0001t0002g0289 a0001c0001t0002g0290 others(1): Show |
6 | NA18953.hp2 NA18971.hp2 NA18977.hp1 others(3): Show |
intron_variant | MODIFIER | c.95-4598T>C | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49502037 | |||||||
| chr13:49502049 | C | G | 1 | a0001c0001t0002g0195 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.95-4586C>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49502049 | |||||||
| chr13:49502071 | G | A | 25 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0016 others(22): Show |
32 | HG01109.hp1 HG01257.hp2 HG02015.hp2 others(29): Show |
intron_variant | MODIFIER | c.95-4564G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49502071 | |||||||
| chr13:49502093 | A | T | 2 | a0003c0006t0001g0066 a0003c0006t0001g0067 |
2 | HG02717.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.95-4542A>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49502093 | |||||||
| chr13:49502213 | A | T | 1 | a0001c0001t0002g0194 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.95-4422A>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49502213 | |||||||
| chr13:49502312 | AATTG | A | 9 | a0001c0001t0001g0133 a0001c0001t0002g0022 a0001c0001t0002g0023 others(6): Show |
11 | HG01106.hp1 HG02486.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.95-4319_95-4316del others(4): Show |
PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 49502312 | ||||||
| chr13:49502622 | C | G | 1 | a0001c0001t0001g0112 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.95-4013C>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49502622 | |||||||
| chr13:49502645 | T | C | 1 | a0001c0001t0001g0224 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.95-3990T>C | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49502645 | |||||||
| chr13:49502745 | G | T | 51 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0042 others(48): Show |
64 | HG00408.hp1 HG00544.hp2 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.95-3890G>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49502745 | |||||||
| chr13:49502779 | G | A | 12 | a0001c0001t0001g0133 a0001c0001t0001g0225 a0001c0001t0001g0226 others(9): Show |
14 | HG01106.hp1 HG01884.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.95-3856G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49502779 | |||||||
| chr13:49503019 | G | A | 1 | a0001c0001t0001g0138 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.95-3616G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49503019 | |||||||
| chr13:49503166 | C | T | 1 | a0001c0002t0001g0097 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.95-3469C>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49503166 | |||||||
| chr13:49503310 | C | T | 41 | a0001c0001t0001g0003 a0001c0001t0001g0196 a0001c0001t0001g0231 others(38): Show |
53 | HG00408.hp1 HG00544.hp2 HG00558.hp1 others(50): Show |
intron_variant | MODIFIER | c.95-3325C>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49503310 | |||||||
| chr13:49503451 | C | T | 1 | a0001c0001t0002g0222 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.95-3184C>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49503451 | |||||||
| chr13:49503484 | C | A | 1 | a0001c0001t0003g0309 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.95-3151C>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49503484 | |||||||
| chr13:49503484 | C | T | 1 | a0001c0001t0001g0113 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.95-3151C>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49503484 | |||||||
| chr13:49503499 | T | C | 1 | a0001c0001t0003g0253 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.95-3136T>C | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49503499 | |||||||
| chr13:49503542 | G | A | 1 | a0001c0002t0001g0102 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.95-3093G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49503542 | |||||||
| chr13:49503705 | C | A | 1 | a0001c0001t0002g0222 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.95-2930C>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49503705 | |||||||
| chr13:49503752 | A | C | 1 | a0001c0001t0001g0143 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.95-2883A>C | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49503752 | |||||||
| chr13:49503762 | T | G | 55 | a0001c0001t0001g0014 a0001c0001t0001g0033 a0001c0001t0001g0034 others(52): Show |
64 | HG00408.hp2 HG00558.hp2 HG00642.hp2 others(61): Show |
intron_variant | MODIFIER | c.95-2873T>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49503762 | |||||||
| chr13:49503961 | T | G | 1 | a0001c0002t0001g0073 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.95-2674T>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49503961 | |||||||
| chr13:49504003 | C | A | 1 | a0001c0001t0002g0291 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.95-2632C>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49504003 | |||||||
| chr13:49504133 | A | C | 1 | a0001c0001t0002g0300 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.95-2502A>C | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49504133 | |||||||
| chr13:49504167 | A | T | 1 | a0001c0001t0002g0183 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.95-2468A>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49504167 | |||||||
| chr13:49504382 | G | A | 2 | a0001c0001t0002g0107 a0001c0001t0002g0108 |
2 | HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.95-2253G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49504382 | |||||||
| chr13:49504481 | CGCCCGGC others(71): Show |
C | 99 | a0001c0001t0001g0154 a0001c0001t0001g0158 a0001c0001t0001g0224 others(96): Show |
128 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(125): Show |
intron_variant | MODIFIER | c.95-2126_95-2049del others(78): Show |
PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 49504481 | ||||||
| chr13:49504486 | G | A | 4 | a0001c0001t0002g0107 a0001c0001t0002g0108 a0001c0001t0002g0136 others(1): Show |
4 | HG02257.hp2 HG03209.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.95-2149G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49504486 | |||||||
| chr13:49504493 | C | T | 3 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0240 |
3 | HG01884.hp2 HG01891.hp1 HG01891.hp2 |
intron_variant | MODIFIER | c.95-2142C>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49504493 | |||||||
| chr13:49504503 | G | A | 55 | a0001c0001t0001g0014 a0001c0001t0001g0033 a0001c0001t0001g0034 others(52): Show |
64 | HG00408.hp2 HG00558.hp2 HG00642.hp2 others(61): Show |
intron_variant | MODIFIER | c.95-2132G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49504503 | |||||||
| chr13:49504513 | GGGCGCCT others(119): Show |
G | 8 | a0001c0001t0001g0072 a0001c0001t0001g0133 a0001c0001t0002g0022 others(5): Show |
9 | HG02280.hp2 HG02486.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.95-2109_95-1984del | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 49504513 | ||||||
| chr13:49504516 | C | T | 1 | a0001c0001t0001g0052 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.95-2119C>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49504516 | |||||||
| chr13:49504526 | T | C | 148 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0014 others(145): Show |
178 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(175): Show |
intron_variant | MODIFIER | c.95-2109T>C | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49504526 | |||||||
| chr13:49504526 | T | TGGCCGCC others(245): Show |
1 | a0001c0001t0001g0116 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.95-2026_95-2025ins others(252): Show |
PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 49504526 | ||||||
| chr13:49504530 | C | T | 1 | a0001c0001t0002g0007 | 2 | HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.95-2105C>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49504530 | |||||||
| chr13:49504591 | T | TGGGGGGT others(42): Show |
105 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0024 others(102): Show |
127 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.95-2001_95-2000ins others(49): Show |
PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 49504591 | ||||||
| chr13:49504610 | C | T | 20 | a0001c0001t0001g0008 a0001c0001t0001g0100 a0001c0001t0001g0115 others(17): Show |
22 | HG00621.hp1 HG01255.hp2 HG01496.hp1 others(19): Show |
intron_variant | MODIFIER | c.95-2025C>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49504610 | |||||||
| chr13:49504627 | C | CCGGGAGG others(42): Show |
2 | a0001c0001t0001g0299 a0001c0001t0001g0321 |
2 | HG01192.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.95-2001_95-2000ins others(49): Show |
PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 49504627 | ||||||
| chr13:49504639 | A | G | 1 | a0001c0001t0001g0116 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.95-1996A>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49504639 | |||||||
| chr13:49504666 | A | G | 107 | a0001c0001t0001g0072 a0001c0001t0001g0133 a0001c0001t0001g0154 others(104): Show |
137 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(134): Show |
intron_variant | MODIFIER | c.95-1969A>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49504666 | |||||||
| chr13:49504715 | A | G | 44 | a0001c0001t0002g0264 a0001c0001t0002g0275 a0001c0001t0003g0004 others(41): Show |
50 | HG00408.hp2 HG00558.hp2 HG00642.hp2 others(47): Show |
intron_variant | MODIFIER | c.95-1920A>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49504715 | |||||||
| chr13:49504732 | G | A | 3 | a0001c0001t0002g0330 a0001c0001t0002g0331 a0001c0001t0002g0332 |
3 | HG01517.hp2 HG01981.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.95-1903G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49504732 | |||||||
| chr13:49504752 | C | G | 1 | a0001c0001t0002g0221 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.95-1883C>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49504752 | |||||||
| chr13:49504761 | G | C | 4 | a0001c0001t0001g0112 a0001c0001t0001g0225 a0001c0001t0001g0226 others(1): Show |
4 | HG01884.hp2 HG01891.hp1 HG01891.hp2 others(1): Show |
intron_variant | MODIFIER | c.95-1874G>C | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49504761 | |||||||
| chr13:49504774 | G | A | 2 | a0001c0001t0001g0046 a0001c0001t0001g0047 |
2 | HG02602.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.95-1861G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49504774 | |||||||
| chr13:49504835 | T | TA | 9 | a0001c0001t0001g0133 a0001c0001t0002g0022 a0001c0001t0002g0023 others(6): Show |
11 | HG01106.hp1 HG02486.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.95-1799dupA | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 49504835 | ||||||
| chr13:49504865 | T | C | 2 | a0001c0001t0001g0286 a0001c0001t0001g0292 |
2 | HG02074.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.95-1770T>C | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49504865 | |||||||
| chr13:49504920 | A | G | 4 | a0001c0001t0002g0107 a0001c0001t0002g0108 a0001c0001t0002g0136 others(1): Show |
4 | HG02257.hp2 HG03209.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.95-1715A>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49504920 | |||||||
| chr13:49505113 | A | T | 1 | a0001c0001t0001g0241 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.95-1522A>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49505113 | |||||||
| chr13:49505146 | G | GA | 8 | a0001c0001t0003g0254 a0001c0001t0003g0255 a0001c0002t0001g0018 others(5): Show |
9 | NA18942.hp2 NA18943.hp1 NA18943.hp2 others(6): Show |
intron_variant | MODIFIER | c.95-1475dupA | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 49505146 | ||||||
| chr13:49505146 | GA | G | 26 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0070 others(23): Show |
28 | HG01106.hp1 HG01109.hp2 HG01256.hp2 others(25): Show |
intron_variant | MODIFIER | c.95-1475delA | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 49505146 | ||||||
| chr13:49505218 | G | A | 1 | a0001c0001t0001g0112 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.95-1417G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49505218 | |||||||
| chr13:49505245 | C | T | 1 | a0001c0001t0002g0056 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.95-1390C>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49505245 | |||||||
| chr13:49505353 | A | G | 4 | a0001c0001t0002g0204 a0001c0001t0002g0205 a0001c0001t0002g0206 others(1): Show |
4 | HG00735.hp2 HG03239.hp2 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.95-1282A>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49505353 | |||||||
| chr13:49505471 | C | A | 1 | a0001c0001t0002g0202 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.95-1164C>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49505471 | |||||||
| chr13:49505625 | G | A | 40 | a0001c0001t0001g0117 a0001c0001t0002g0264 a0001c0001t0002g0275 others(37): Show |
46 | HG00408.hp2 HG00558.hp2 HG00642.hp2 others(43): Show |
intron_variant | MODIFIER | c.95-1010G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49505625 | |||||||
| chr13:49505787 | C | T | 1 | a0001c0001t0001g0068 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.95-848C>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49505787 | |||||||
| chr13:49505926 | G | A | 4 | a0001c0001t0002g0107 a0001c0001t0002g0108 a0001c0001t0002g0136 others(1): Show |
4 | HG02257.hp2 HG03209.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.95-709G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49505926 | |||||||
| chr13:49505988 | C | A | 1 | a0001c0001t0003g0256 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.95-647C>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49505988 | |||||||
| chr13:49506223 | C | A | 1 | a0001c0001t0001g0113 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.95-412C>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49506223 | |||||||
| chr13:49506233 | T | TA | 17 | a0001c0001t0001g0024 a0001c0001t0001g0042 a0001c0001t0001g0048 others(14): Show |
18 | HG00733.hp1 HG01243.hp1 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.95-383dupA | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 49506233 | ||||||
| chr13:49506233 | TA | T | 7 | a0001c0001t0001g0117 a0001c0001t0001g0233 a0001c0001t0001g0247 others(4): Show |
7 | HG01099.hp1 HG02897.hp1 HG03490.hp2 others(4): Show |
intron_variant | MODIFIER | c.95-383delA | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 49506233 | ||||||
| chr13:49506325 | G | A | 6 | a0001c0001t0001g0024 a0001c0001t0001g0138 a0001c0001t0001g0139 others(3): Show |
7 | HG01074.hp1 HG01243.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.95-310G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49506325 | |||||||
| chr13:49506456 | A | G | 21 | a0001c0001t0001g0008 a0001c0001t0001g0100 a0001c0001t0001g0115 others(18): Show |
23 | HG00621.hp1 HG01255.hp2 HG01496.hp1 others(20): Show |
intron_variant | MODIFIER | c.95-179A>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49506456 | |||||||
| chr13:49506501 | A | C | 1 | a0001c0001t0002g0136 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.95-134A>C | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 1/9 | chr13 | 49506501 | |||||||
| chr13:49506861 | A | G | 1 | a0001c0001t0001g0100 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.216+105A>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | chr13 | 49506861 | |||||||
| chr13:49506898 | C | CT | 230 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0014 others(227): Show |
294 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(291): Show |
intron_variant | MODIFIER | c.216+165dupT | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr13 | 49506898 | ||||||
| chr13:49506898 | C | CTT | 23 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0100 others(20): Show |
23 | HG00099.hp1 HG00609.hp1 HG00741.hp1 others(20): Show |
intron_variant | MODIFIER | c.216+164_216+165dup others(2): Show |
PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr13 | 49506898 | ||||||
| chr13:49506898 | CT | C | 8 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0070 others(5): Show |
8 | HG01109.hp2 HG01891.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.216+165delT | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr13 | 49506898 | ||||||
| chr13:49506924 | G | A | 11 | a0001c0001t0001g0133 a0001c0001t0001g0226 a0001c0001t0001g0240 others(8): Show |
13 | HG01106.hp1 HG01884.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.216+168G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | chr13 | 49506924 | |||||||
| chr13:49506997 | G | A | 2 | a0001c0001t0002g0153 a0001c0001t0002g0187 |
2 | HG01192.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.216+241G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | chr13 | 49506997 | |||||||
| chr13:49507004 | C | T | 2 | a0003c0006t0001g0066 a0003c0006t0001g0067 |
2 | HG02717.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.216+248C>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | chr13 | 49507004 | |||||||
| chr13:49507032 | T | C | 1 | a0001c0001t0001g0241 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.216+276T>C | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | chr13 | 49507032 | |||||||
| chr13:49507048 | T | C | 1 | a0001c0001t0002g0202 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.216+292T>C | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | chr13 | 49507048 | |||||||
| chr13:49507070 | A | AT | 6 | a0001c0001t0001g0024 a0001c0001t0001g0138 a0001c0001t0001g0139 others(3): Show |
7 | HG01074.hp1 HG01243.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.216+322dupT | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr13 | 49507070 | ||||||
| chr13:49507138 | C | T | 1 | a0001c0001t0002g0176 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.216+382C>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | chr13 | 49507138 | |||||||
| chr13:49507187 | G | A | 5 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0070 others(2): Show |
5 | HG01109.hp2 HG02647.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.216+431G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | chr13 | 49507187 | |||||||
| chr13:49507222 | C | T | 99 | a0001c0001t0001g0158 a0001c0001t0001g0224 a0001c0001t0002g0001 others(96): Show |
130 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.216+466C>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | chr13 | 49507222 | |||||||
| chr13:49507382 | A | G | 1 | a0001c0001t0001g0224 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.216+626A>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | chr13 | 49507382 | |||||||
| chr13:49507744 | T | G | 1 | a0001c0001t0002g0130 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.216+988T>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | chr13 | 49507744 | |||||||
| chr13:49507960 | C | T | 1 | a0001c0005t0002g0175 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.216+1204C>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | chr13 | 49507960 | |||||||
| chr13:49508120 | A | G | 260 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0014 others(257): Show |
320 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(317): Show |
intron_variant | MODIFIER | c.216+1364A>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | chr13 | 49508120 | |||||||
| chr13:49508153 | A | G | 1 | a0001c0001t0002g0128 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.216+1397A>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | chr13 | 49508153 | |||||||
| chr13:49508160 | A | ATATGTAT others(19): Show |
14 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0046 others(11): Show |
17 | HG01070.hp1 HG01257.hp2 HG02015.hp2 others(14): Show |
intron_variant | MODIFIER | c.216+1428_216+1453d others(28): Show |
PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr13 | 49508160 | ||||||
| chr13:49508160 | A | ATATGTAT others(45): Show |
1 | a0001c0001t0001g0051 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.216+1453_216+1454i others(54): Show |
PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr13 | 49508160 | ||||||
| chr13:49508186 | G | GTATGTAT others(19): Show |
51 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0042 others(48): Show |
64 | HG00408.hp1 HG00544.hp2 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.216+1450_216+1475d others(28): Show |
PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr13 | 49508186 | ||||||
| chr13:49508258 | G | A | 1 | a0001c0002t0001g0079 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.216+1502G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | chr13 | 49508258 | |||||||
| chr13:49508297 | A | G | 11 | a0001c0001t0001g0133 a0001c0001t0001g0226 a0001c0001t0001g0240 others(8): Show |
13 | HG01106.hp1 HG01884.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.216+1541A>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | chr13 | 49508297 | |||||||
| chr13:49508319 | AATATATT others(9): Show |
A | 66 | a0001c0001t0001g0014 a0001c0001t0001g0033 a0001c0001t0001g0034 others(63): Show |
75 | HG00408.hp2 HG00558.hp2 HG00642.hp2 others(72): Show |
intron_variant | MODIFIER | c.216+1587_216+1602d others(18): Show |
PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr13 | 49508319 | ||||||
| chr13:49508332 | A | G | 4 | a0001c0001t0001g0042 a0001c0001t0001g0109 a0001c0001t0001g0110 others(1): Show |
4 | HG02895.hp2 HG02897.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.216+1576A>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | chr13 | 49508332 | |||||||
| chr13:49508336 | A | C | 60 | a0001c0001t0001g0014 a0001c0001t0001g0033 a0001c0001t0001g0034 others(57): Show |
69 | HG00408.hp2 HG00558.hp2 HG00642.hp2 others(66): Show |
intron_variant | MODIFIER | c.216+1580A>C | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | chr13 | 49508336 | |||||||
| chr13:49508343 | A | C | 2 | a0001c0001t0001g0226 a0001c0001t0001g0240 |
2 | HG01884.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.216+1587A>C | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | chr13 | 49508343 | |||||||
| chr13:49508344 | C | A | 2 | a0001c0001t0001g0226 a0001c0001t0001g0240 |
2 | HG01884.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.216+1588C>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | chr13 | 49508344 | |||||||
| chr13:49508352 | A | T | 60 | a0001c0001t0001g0014 a0001c0001t0001g0033 a0001c0001t0001g0034 others(57): Show |
69 | HG00408.hp2 HG00558.hp2 HG00642.hp2 others(66): Show |
intron_variant | MODIFIER | c.216+1596A>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | chr13 | 49508352 | |||||||
| chr13:49508536 | T | G | 4 | a0001c0001t0002g0107 a0001c0001t0002g0108 a0001c0001t0002g0136 others(1): Show |
4 | HG02257.hp2 HG03209.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.216+1780T>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | chr13 | 49508536 | |||||||
| chr13:49508612 | T | C | 1 | a0001c0001t0002g0199 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.216+1856T>C | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | chr13 | 49508612 | |||||||
| chr13:49508846 | C | T | 1 | a0001c0005t0002g0175 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.216+2090C>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | chr13 | 49508846 | |||||||
| chr13:49508965 | A | G | 1 | a0001c0001t0001g0113 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.216+2209A>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | chr13 | 49508965 | |||||||
| chr13:49509214 | A | AT | 114 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0024 others(111): Show |
135 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(132): Show |
intron_variant | MODIFIER | c.216+2473dupT | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr13 | 49509214 | ||||||
| chr13:49509214 | AT | A | 24 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0070 others(21): Show |
27 | HG01074.hp2 HG01081.hp1 HG01106.hp1 others(24): Show |
intron_variant | MODIFIER | c.216+2473delT | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr13 | 49509214 | ||||||
| chr13:49509276 | G | T | 2 | a0001c0001t0001g0072 a0001c0001t0001g0225 |
2 | HG01891.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.216+2520G>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | chr13 | 49509276 | |||||||
| chr13:49509376 | C | T | 55 | a0001c0001t0001g0014 a0001c0001t0001g0033 a0001c0001t0001g0034 others(52): Show |
64 | HG00408.hp2 HG00558.hp2 HG00642.hp2 others(61): Show |
intron_variant | MODIFIER | c.216+2620C>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | chr13 | 49509376 | |||||||
| chr13:49509446 | C | T | 2 | a0001c0001t0001g0226 a0001c0001t0001g0240 |
2 | HG01884.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.216+2690C>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | chr13 | 49509446 | |||||||
| chr13:49509462 | C | T | 55 | a0001c0001t0001g0014 a0001c0001t0001g0033 a0001c0001t0001g0034 others(52): Show |
64 | HG00408.hp2 HG00558.hp2 HG00642.hp2 others(61): Show |
intron_variant | MODIFIER | c.216+2706C>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | chr13 | 49509462 | |||||||
| chr13:49509520 | T | C | 16 | a0001c0001t0001g0014 a0001c0001t0001g0033 a0001c0001t0001g0034 others(13): Show |
19 | HG01243.hp2 HG01884.hp1 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.216+2764T>C | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | chr13 | 49509520 | |||||||
| chr13:49509562 | C | G | 1 | a0001c0002t0001g0102 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.216+2806C>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | chr13 | 49509562 | |||||||
| chr13:49509745 | A | G | 1 | a0001c0001t0003g0278 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.216+2989A>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | chr13 | 49509745 | |||||||
| chr13:49509831 | T | G | 1 | a0001c0001t0002g0129 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.216+3075T>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | chr13 | 49509831 | |||||||
| chr13:49510012 | C | CGT | 12 | a0001c0001t0001g0024 a0001c0001t0001g0042 a0001c0001t0001g0109 others(9): Show |
13 | HG01074.hp1 HG01243.hp1 HG01255.hp2 others(10): Show |
intron_variant | MODIFIER | c.217-3029_217-3028d others(4): Show |
PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr13 | 49510012 | ||||||
| chr13:49510135 | C | A | 5 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0070 others(2): Show |
5 | HG01109.hp2 HG02647.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.217-2924C>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | chr13 | 49510135 | |||||||
| chr13:49510201 | C | T | 16 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0070 others(13): Show |
18 | HG01106.hp1 HG01109.hp2 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.217-2858C>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | chr13 | 49510201 | |||||||
| chr13:49510207 | G | T | 2 | a0001c0001t0002g0172 a0001c0001t0002g0173 |
2 | HG00099.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.217-2852G>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | chr13 | 49510207 | |||||||
| chr13:49510286 | A | G | 55 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0042 others(52): Show |
68 | HG00408.hp1 HG00544.hp2 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.217-2773A>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | chr13 | 49510286 | |||||||
| chr13:49510344 | A | G | 1 | a0001c0001t0002g0183 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.217-2715A>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | chr13 | 49510344 | |||||||
| chr13:49510700 | G | A | 1 | a0001c0001t0001g0293 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.217-2359G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | chr13 | 49510700 | |||||||
| chr13:49511073 | T | C | 2 | a0001c0001t0001g0015 a0001c0001t0001g0054 |
3 | NA18947.hp1 NA18962.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.217-1986T>C | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | chr13 | 49511073 | |||||||
| chr13:49511127 | A | G | 42 | a0001c0001t0001g0003 a0001c0001t0001g0196 a0001c0001t0001g0231 others(39): Show |
54 | HG00408.hp1 HG00544.hp2 HG00558.hp1 others(51): Show |
intron_variant | MODIFIER | c.217-1932A>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | chr13 | 49511127 | |||||||
| chr13:49511327 | C | CTT | 207 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(204): Show |
265 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(262): Show |
intron_variant | MODIFIER | c.217-1717_217-1716d others(4): Show |
PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr13 | 49511327 | ||||||
| chr13:49511327 | C | CTTT | 47 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0100 others(44): Show |
49 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(46): Show |
intron_variant | MODIFIER | c.217-1718_217-1716d others(5): Show |
PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr13 | 49511327 | ||||||
| chr13:49511327 | CT | C | 18 | a0001c0001t0001g0014 a0001c0001t0001g0024 a0001c0001t0001g0043 others(15): Show |
20 | HG01074.hp1 HG01243.hp1 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.217-1716delT | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr13 | 49511327 | ||||||
| chr13:49511349 | G | T | 1 | a0001c0001t0001g0070 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.217-1710G>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | chr13 | 49511349 | |||||||
| chr13:49511357 | G | A | 1 | a0001c0002t0001g0079 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.217-1702G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | chr13 | 49511357 | |||||||
| chr13:49511387 | C | T | 46 | a0001c0001t0001g0003 a0001c0001t0001g0034 a0001c0001t0001g0196 others(43): Show |
59 | HG00408.hp1 HG00544.hp2 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.217-1672C>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | chr13 | 49511387 | |||||||
| chr13:49511404 | G | A | 2 | a0001c0001t0002g0155 a0001c0001t0002g0192 |
2 | HG01123.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.217-1655G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | chr13 | 49511404 | |||||||
| chr13:49511413 | G | A | 14 | a0001c0001t0001g0008 a0001c0001t0001g0100 a0001c0001t0001g0115 others(11): Show |
16 | HG00621.hp1 HG02165.hp1 HG02738.hp1 others(13): Show |
intron_variant | MODIFIER | c.217-1646G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | chr13 | 49511413 | |||||||
| chr13:49511682 | G | T | 1 | a0001c0001t0001g0226 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.217-1377G>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | chr13 | 49511682 | |||||||
| chr13:49511734 | C | A | 1 | a0001c0001t0002g0136 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.217-1325C>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | chr13 | 49511734 | |||||||
| chr13:49511742 | A | G | 2 | a0001c0001t0001g0072 a0001c0001t0001g0225 |
2 | HG01891.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.217-1317A>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | chr13 | 49511742 | |||||||
| chr13:49512108 | A | G | 101 | a0001c0001t0001g0158 a0001c0001t0002g0001 a0001c0001t0002g0007 others(98): Show |
132 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.217-951A>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | chr13 | 49512108 | |||||||
| chr13:49512117 | T | G | 34 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0016 others(31): Show |
41 | HG01070.hp1 HG01109.hp1 HG01257.hp2 others(38): Show |
intron_variant | MODIFIER | c.217-942T>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | chr13 | 49512117 | |||||||
| chr13:49512130 | G | T | 102 | a0001c0001t0001g0158 a0001c0001t0001g0224 a0001c0001t0002g0001 others(99): Show |
133 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(130): Show |
intron_variant | MODIFIER | c.217-929G>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | chr13 | 49512130 | |||||||
| chr13:49512190 | T | A | 261 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(258): Show |
321 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(318): Show |
intron_variant | MODIFIER | c.217-869T>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | chr13 | 49512190 | |||||||
| chr13:49512293 | T | G | 1 | a0001c0001t0002g0156 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.217-766T>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | chr13 | 49512293 | |||||||
| chr13:49512314 | C | T | 34 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0016 others(31): Show |
41 | HG01070.hp1 HG01109.hp1 HG01257.hp2 others(38): Show |
intron_variant | MODIFIER | c.217-745C>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | chr13 | 49512314 | |||||||
| chr13:49512354 | T | G | 1 | a0001c0001t0001g0113 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.217-705T>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | chr13 | 49512354 | |||||||
| chr13:49512734 | C | G | 1 | a0001c0001t0002g0129 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.217-325C>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | chr13 | 49512734 | |||||||
| chr13:49512973 | G | T | 2 | a0001c0001t0001g0072 a0001c0001t0001g0225 |
2 | HG01891.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.217-86G>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | chr13 | 49512973 | |||||||
| chr13:49513006 | T | C | 72 | a0001c0001t0001g0158 a0001c0001t0002g0001 a0001c0001t0002g0009 others(69): Show |
97 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.217-53T>C | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 2/9 | chr13 | 49513006 | |||||||
| chr13:49513328 | A | AT | 49 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0015 others(46): Show |
58 | HG01070.hp1 HG01074.hp1 HG01109.hp1 others(55): Show |
intron_variant | MODIFIER | c.324+181dupT | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr13 | 49513328 | ||||||
| chr13:49513328 | AT | A | 114 | a0001c0001t0001g0110 a0001c0001t0001g0133 a0001c0001t0001g0158 others(111): Show |
147 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.324+181delT | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr13 | 49513328 | ||||||
| chr13:49513328 | ATT | A | 11 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0112 others(8): Show |
11 | HG00673.hp1 HG01109.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.324+180_324+181del others(2): Show |
PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr13 | 49513328 | ||||||
| chr13:49513351 | A | G | 4 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0112 others(1): Show |
4 | HG01109.hp2 HG02647.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.324+185A>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 3/9 | chr13 | 49513351 | |||||||
| chr13:49513392 | A | G | 261 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(258): Show |
321 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(318): Show |
intron_variant | MODIFIER | c.324+226A>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 3/9 | chr13 | 49513392 | |||||||
| chr13:49513403 | TCACTGCA others(20): Show |
T | 1 | a0001c0001t0001g0111 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.324+238_324+264del others(27): Show |
PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 3/9 | chr13 | 49513403 | |||||||
| chr13:49513446 | T | A | 1 | a0001c0001t0001g0111 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.324+280T>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 3/9 | chr13 | 49513446 | |||||||
| chr13:49513449 | G | A | 1 | a0001c0001t0002g0275 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.324+283G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 3/9 | chr13 | 49513449 | |||||||
| chr13:49513450 | C | T | 1 | a0001c0001t0001g0111 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.324+284C>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 3/9 | chr13 | 49513450 | |||||||
| chr13:49513451 | C | G | 1 | a0001c0001t0001g0111 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.324+285C>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 3/9 | chr13 | 49513451 | |||||||
| chr13:49513452 | T | A | 1 | a0001c0001t0001g0111 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.324+286T>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 3/9 | chr13 | 49513452 | |||||||
| chr13:49513454 | C | G | 1 | a0001c0001t0001g0111 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.324+288C>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 3/9 | chr13 | 49513454 | |||||||
| chr13:49513456 | G | A | 1 | a0001c0001t0001g0292 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.324+290G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 3/9 | chr13 | 49513456 | |||||||
| chr13:49513530 | C | T | 11 | a0001c0001t0001g0133 a0001c0001t0001g0226 a0001c0001t0001g0240 others(8): Show |
13 | HG01106.hp1 HG01884.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.324+364C>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 3/9 | chr13 | 49513530 | |||||||
| chr13:49513539 | C | T | 20 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0038 others(17): Show |
26 | HG00408.hp1 HG01952.hp1 HG01978.hp1 others(23): Show |
intron_variant | MODIFIER | c.324+373C>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 3/9 | chr13 | 49513539 | |||||||
| chr13:49513613 | G | T | 1 | a0001c0001t0002g0165 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.324+447G>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 3/9 | chr13 | 49513613 | |||||||
| chr13:49513640 | TA | T | 102 | a0001c0001t0001g0158 a0001c0001t0001g0224 a0001c0001t0002g0001 others(99): Show |
133 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(130): Show |
intron_variant | MODIFIER | c.324+475delA | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 3/9 | chr13 | 49513640 | |||||||
| chr13:49513874 | C | T | 19 | a0001c0001t0001g0008 a0001c0001t0001g0100 a0001c0001t0001g0115 others(16): Show |
21 | HG00621.hp1 HG01255.hp2 HG01496.hp1 others(18): Show |
intron_variant | MODIFIER | c.324+708C>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 3/9 | chr13 | 49513874 | |||||||
| chr13:49513877 | T | C | 19 | a0001c0001t0001g0008 a0001c0001t0001g0100 a0001c0001t0001g0115 others(16): Show |
21 | HG00621.hp1 HG01255.hp2 HG01496.hp1 others(18): Show |
intron_variant | MODIFIER | c.324+711T>C | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 3/9 | chr13 | 49513877 | |||||||
| chr13:49513896 | G | A | 2 | a0003c0006t0001g0066 a0003c0006t0001g0067 |
2 | HG02717.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.324+730G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 3/9 | chr13 | 49513896 | |||||||
| chr13:49513927 | G | A | 1 | a0001c0001t0001g0048 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.324+761G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 3/9 | chr13 | 49513927 | |||||||
| chr13:49513997 | G | T | 34 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0016 others(31): Show |
41 | HG01070.hp1 HG01109.hp1 HG01257.hp2 others(38): Show |
intron_variant | MODIFIER | c.324+831G>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 3/9 | chr13 | 49513997 | |||||||
| chr13:49514020 | A | G | 1 | a0001c0001t0002g0230 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.324+854A>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 3/9 | chr13 | 49514020 | |||||||
| chr13:49514314 | G | C | 1 | a0001c0001t0003g0260 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.324+1148G>C | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 3/9 | chr13 | 49514314 | |||||||
| chr13:49514709 | G | C | 1 | a0001c0002t0001g0325 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.324+1543G>C | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 3/9 | chr13 | 49514709 | |||||||
| chr13:49514762 | TA | T | 219 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0015 others(216): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.324+1611delA | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr13 | 49514762 | ||||||
| chr13:49514939 | A | G | 1 | a0001c0001t0001g0226 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.324+1773A>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 3/9 | chr13 | 49514939 | |||||||
| chr13:49515109 | G | A | 4 | a0001c0002t0001g0019 a0001c0002t0001g0081 a0001c0002t0001g0082 others(1): Show |
5 | HG00609.hp2 HG02083.hp2 HG02165.hp2 others(2): Show |
intron_variant | MODIFIER | c.324+1943G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 3/9 | chr13 | 49515109 | |||||||
| chr13:49515138 | G | A | 14 | a0001c0002t0001g0013 a0001c0002t0001g0039 a0001c0002t0001g0040 others(11): Show |
18 | HG00280.hp1 HG00639.hp2 HG00741.hp2 others(15): Show |
intron_variant | MODIFIER | c.324+1972G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 3/9 | chr13 | 49515138 | |||||||
| chr13:49515335 | C | T | 34 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0016 others(31): Show |
41 | HG01070.hp1 HG01109.hp1 HG01257.hp2 others(38): Show |
intron_variant | MODIFIER | c.324+2169C>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 3/9 | chr13 | 49515335 | |||||||
| chr13:49515455 | T | TAC | 20 | a0001c0001t0001g0100 a0001c0001t0001g0117 a0001c0001t0001g0120 others(17): Show |
31 | HG00140.hp1 HG00140.hp2 HG00733.hp2 others(28): Show |
intron_variant | MODIFIER | c.324+2337_324+2338d others(4): Show |
PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr13 | 49515455 | ||||||
| chr13:49515455 | T | TACAC | 7 | a0001c0001t0001g0125 a0001c0001t0002g0204 a0001c0002t0001g0080 others(4): Show |
7 | HG00735.hp1 HG01106.hp2 HG01934.hp1 others(4): Show |
intron_variant | MODIFIER | c.324+2335_324+2338d others(6): Show |
PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr13 | 49515455 | ||||||
| chr13:49515455 | T | TACACACA others(1): Show |
3 | a0001c0002t0001g0084 a0001c0002t0001g0089 a0001c0002t0001g0104 |
3 | HG01070.hp2 HG01071.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.324+2331_324+2338d others(10): Show |
PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr13 | 49515455 | ||||||
| chr13:49515455 | TAC | T | 11 | a0001c0001t0001g0072 a0001c0001t0002g0026 a0001c0001t0002g0128 others(8): Show |
12 | HG00099.hp1 HG00609.hp2 HG00642.hp2 others(9): Show |
intron_variant | MODIFIER | c.324+2337_324+2338d others(4): Show |
PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr13 | 49515455 | ||||||
| chr13:49515455 | TACAC | T | 39 | a0001c0001t0001g0014 a0001c0001t0001g0043 a0001c0001t0001g0044 others(36): Show |
45 | HG00408.hp2 HG00741.hp1 HG01168.hp1 others(42): Show |
intron_variant | MODIFIER | c.324+2335_324+2338d others(6): Show |
PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr13 | 49515455 | ||||||
| chr13:49515455 | TACACAC | T | 45 | a0001c0001t0001g0024 a0001c0001t0001g0042 a0001c0001t0001g0069 others(42): Show |
56 | HG00558.hp2 HG00639.hp2 HG00741.hp2 others(53): Show |
intron_variant | MODIFIER | c.324+2333_324+2338d others(8): Show |
PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr13 | 49515455 | ||||||
| chr13:49515455 | TACACACA others(1): Show |
T | 20 | a0001c0001t0001g0226 a0001c0001t0001g0242 a0001c0001t0001g0243 others(17): Show |
22 | HG00280.hp1 HG01243.hp2 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.324+2331_324+2338d others(10): Show |
PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr13 | 49515455 | ||||||
| chr13:49515455 | TACACACA others(3): Show |
T | 5 | a0001c0001t0001g0241 a0001c0001t0002g0023 a0001c0001t0002g0129 others(2): Show |
6 | HG01106.hp1 HG01123.hp2 HG02155.hp2 others(3): Show |
intron_variant | MODIFIER | c.324+2329_324+2338d others(12): Show |
PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr13 | 49515455 | ||||||
| chr13:49515455 | TACACACA others(7): Show |
T | 7 | a0001c0001t0001g0133 a0001c0001t0002g0022 a0001c0001t0002g0130 others(4): Show |
8 | HG02486.hp1 HG03098.hp1 HG03209.hp2 others(5): Show |
intron_variant | MODIFIER | c.324+2325_324+2338d others(16): Show |
PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr13 | 49515455 | ||||||
| chr13:49515455 | TACACACA others(9): Show |
T | 49 | a0001c0001t0001g0003 a0001c0001t0001g0196 a0001c0001t0001g0231 others(46): Show |
62 | HG00408.hp1 HG00544.hp2 HG00558.hp1 others(59): Show |
intron_variant | MODIFIER | c.324+2323_324+2338d others(18): Show |
PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr13 | 49515455 | ||||||
| chr13:49515455 | TACACACA others(11): Show |
T | 63 | a0001c0001t0001g0158 a0001c0001t0002g0001 a0001c0001t0002g0009 others(60): Show |
87 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.324+2321_324+2338d others(20): Show |
PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr13 | 49515455 | ||||||
| chr13:49515455 | TACACACA others(15): Show |
T | 1 | a0001c0001t0002g0191 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.324+2317_324+2338d others(24): Show |
PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr13 | 49515455 | ||||||
| chr13:49515455 | TACACACA others(17): Show |
T | 33 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0016 others(30): Show |
40 | HG01070.hp1 HG01109.hp1 HG02015.hp2 others(37): Show |
intron_variant | MODIFIER | c.324+2315_324+2338d others(26): Show |
PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr13 | 49515455 | ||||||
| chr13:49515455 | TACACACA others(21): Show |
T | 2 | a0001c0001t0001g0053 a0001c0001t0002g0164 |
2 | HG01257.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.324+2311_324+2338d others(30): Show |
PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr13 | 49515455 | ||||||
| chr13:49515489 | CACACACA others(8): Show |
C | 1 | a0001c0001t0001g0141 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.324+2324_324+2338d others(17): Show |
PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 3/9 | chr13 | 49515489 | |||||||
| chr13:49515507 | C | A | 2 | a0001c0001t0001g0299 a0001c0001t0001g0321 |
2 | HG01192.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.324+2341C>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 3/9 | chr13 | 49515507 | |||||||
| chr13:49515547 | C | A | 14 | a0001c0001t0001g0008 a0001c0001t0001g0100 a0001c0001t0001g0115 others(11): Show |
16 | HG00621.hp1 HG02165.hp1 HG02738.hp1 others(13): Show |
intron_variant | MODIFIER | c.324+2381C>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 3/9 | chr13 | 49515547 | |||||||
| chr13:49515708 | C | T | 87 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(84): Show |
104 | HG00544.hp2 HG00558.hp1 HG00597.hp2 others(101): Show |
intron_variant | MODIFIER | c.325-2310C>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 3/9 | chr13 | 49515708 | |||||||
| chr13:49515733 | G | A | 4 | a0001c0001t0002g0012 a0001c0001t0002g0289 a0001c0001t0002g0290 others(1): Show |
6 | NA18953.hp2 NA18971.hp2 NA18977.hp1 others(3): Show |
intron_variant | MODIFIER | c.325-2285G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 3/9 | chr13 | 49515733 | |||||||
| chr13:49515889 | C | T | 263 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(260): Show |
323 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(320): Show |
intron_variant | MODIFIER | c.325-2129C>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 3/9 | chr13 | 49515889 | |||||||
| chr13:49516069 | G | A | 1 | a0001c0001t0001g0158 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.325-1949G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 3/9 | chr13 | 49516069 | |||||||
| chr13:49516176 | A | C | 53 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0042 others(50): Show |
63 | HG00544.hp2 HG00558.hp1 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.325-1842A>C | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 3/9 | chr13 | 49516176 | |||||||
| chr13:49516321 | C | G | 1 | a0001c0001t0002g0151 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.325-1697C>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 3/9 | chr13 | 49516321 | |||||||
| chr13:49516335 | A | G | 1 | a0001c0002t0001g0102 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.325-1683A>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 3/9 | chr13 | 49516335 | |||||||
| chr13:49516338 | C | G | 1 | a0001c0001t0002g0151 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.325-1680C>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 3/9 | chr13 | 49516338 | |||||||
| chr13:49516494 | T | C | 24 | a0001c0001t0001g0003 a0001c0001t0001g0042 a0001c0001t0001g0109 others(21): Show |
30 | HG00544.hp2 HG00558.hp1 HG00597.hp2 others(27): Show |
intron_variant | MODIFIER | c.325-1524T>C | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 3/9 | chr13 | 49516494 | |||||||
| chr13:49516586 | T | G | 1 | a0001c0001t0002g0149 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.325-1432T>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 3/9 | chr13 | 49516586 | |||||||
| chr13:49516708 | C | A | 253 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(250): Show |
312 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(309): Show |
intron_variant | MODIFIER | c.325-1310C>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 3/9 | chr13 | 49516708 | |||||||
| chr13:49516745 | C | T | 1 | a0001c0001t0002g0183 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.325-1273C>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 3/9 | chr13 | 49516745 | |||||||
| chr13:49516965 | C | T | 1 | a0001c0001t0002g0291 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.325-1053C>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 3/9 | chr13 | 49516965 | |||||||
| chr13:49516972 | C | T | 14 | a0001c0002t0001g0013 a0001c0002t0001g0039 a0001c0002t0001g0040 others(11): Show |
18 | HG00280.hp1 HG00639.hp2 HG00741.hp2 others(15): Show |
intron_variant | MODIFIER | c.325-1046C>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 3/9 | chr13 | 49516972 | |||||||
| chr13:49516974 | A | G | 1 | a0001c0001t0001g0111 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.325-1044A>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 3/9 | chr13 | 49516974 | |||||||
| chr13:49517013 | T | C | 1 | a0001c0002t0001g0098 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.325-1005T>C | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 3/9 | chr13 | 49517013 | |||||||
| chr13:49517022 | C | T | 4 | a0001c0001t0001g0016 a0001c0001t0001g0058 a0001c0001t0001g0059 others(1): Show |
5 | HG01109.hp1 HG02451.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.325-996C>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 3/9 | chr13 | 49517022 | |||||||
| chr13:49517598 | G | GAGA | 13 | a0001c0001t0001g0014 a0001c0001t0001g0033 a0001c0001t0001g0034 others(10): Show |
16 | HG02109.hp1 HG02257.hp1 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.325-418_325-416dup others(3): Show |
PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr13 | 49517598 | ||||||
| chr13:49517736 | G | C | 1 | a0001c0001t0001g0142 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.325-282G>C | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 3/9 | chr13 | 49517736 | |||||||
| chr13:49517956 | C | G | 1 | a0001c0001t0001g0100 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.325-62C>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 3/9 | chr13 | 49517956 | |||||||
| chr13:49517991 | TACTC | T | 226 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0014 others(223): Show |
280 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(277): Show |
intron_variant | MODIFIER | c.325-25_325-22delCT others(2): Show |
PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr13 | 49517991 | ||||||
| chr13:49518193 | G | A | 1 | a0003c0006t0001g0066 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.458+42G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 4/9 | chr13 | 49518193 | |||||||
| chr13:49518324 | CTA | C | 263 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(260): Show |
323 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(320): Show |
intron_variant | MODIFIER | c.458+189_458+190del others(2): Show |
PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr13 | 49518324 | ||||||
| chr13:49518330 | A | C | 1 | a0001c0001t0003g0255 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.458+179A>C | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 4/9 | chr13 | 49518330 | |||||||
| chr13:49518330 | A | T | 1 | a0001c0002t0001g0103 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.458+179A>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 4/9 | chr13 | 49518330 | |||||||
| chr13:49518331 | T | A | 1 | a0001c0002t0001g0103 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.458+180T>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 4/9 | chr13 | 49518331 | |||||||
| chr13:49518350 | T | C | 226 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0014 others(223): Show |
280 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(277): Show |
intron_variant | MODIFIER | c.458+199T>C | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 4/9 | chr13 | 49518350 | |||||||
| chr13:49518429 | C | T | 2 | a0003c0006t0001g0066 a0003c0006t0001g0067 |
2 | HG02717.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.458+278C>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 4/9 | chr13 | 49518429 | |||||||
| chr13:49518460 | G | T | 15 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0112 others(12): Show |
17 | HG01106.hp1 HG01109.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.458+309G>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 4/9 | chr13 | 49518460 | |||||||
| chr13:49518597 | T | TTAATCCT others(22): Show |
1 | a0001c0002t0001g0103 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.458+449_458+477dup others(29): Show |
PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr13 | 49518597 | ||||||
| chr13:49518705 | G | A | 15 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0112 others(12): Show |
17 | HG01106.hp1 HG01109.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.458+554G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 4/9 | chr13 | 49518705 | |||||||
| chr13:49518711 | G | A | 124 | a0001c0001t0001g0158 a0001c0001t0001g0224 a0001c0001t0002g0001 others(121): Show |
161 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.458+560G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 4/9 | chr13 | 49518711 | |||||||
| chr13:49518717 | G | A | 9 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0068 others(6): Show |
11 | HG02109.hp1 HG02257.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.458+566G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 4/9 | chr13 | 49518717 | |||||||
| chr13:49518834 | A | AT | 55 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0016 others(52): Show |
64 | HG00280.hp1 HG00544.hp2 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.458+702dupT | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr13 | 49518834 | ||||||
| chr13:49518834 | A | ATT | 6 | a0001c0001t0001g0122 a0002c0003t0001g0017 a0002c0003t0001g0041 others(3): Show |
7 | HG00621.hp1 HG02109.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.458+701_458+702dup others(2): Show |
PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr13 | 49518834 | ||||||
| chr13:49518834 | A | ATTT | 9 | a0001c0001t0001g0133 a0001c0001t0001g0226 a0001c0001t0002g0022 others(6): Show |
11 | HG01106.hp1 HG01884.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.458+700_458+702dup others(3): Show |
PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr13 | 49518834 | ||||||
| chr13:49518834 | A | ATTTT | 6 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0112 others(3): Show |
6 | HG01109.hp2 HG01891.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.458+699_458+702dup others(4): Show |
PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr13 | 49518834 | ||||||
| chr13:49518834 | AT | A | 115 | a0001c0001t0001g0158 a0001c0001t0002g0001 a0001c0001t0002g0005 others(112): Show |
152 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.458+702delT | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr13 | 49518834 | ||||||
| chr13:49518839 | T | A | 1 | a0001c0001t0002g0168 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.458+688T>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 4/9 | chr13 | 49518839 | |||||||
| chr13:49518859 | A | G | 4 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0112 others(1): Show |
4 | HG01109.hp2 HG02647.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.458+708A>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 4/9 | chr13 | 49518859 | |||||||
| chr13:49518898 | C | G | 71 | a0001c0001t0001g0158 a0001c0001t0002g0001 a0001c0001t0002g0009 others(68): Show |
95 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.458+747C>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 4/9 | chr13 | 49518898 | |||||||
| chr13:49518899 | G | A | 1 | a0001c0001t0001g0068 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.458+748G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 4/9 | chr13 | 49518899 | |||||||
| chr13:49518960 | C | T | 109 | a0001c0001t0001g0158 a0001c0001t0002g0001 a0001c0001t0002g0005 others(106): Show |
142 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.458+809C>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 4/9 | chr13 | 49518960 | |||||||
| chr13:49518961 | G | A | 11 | a0001c0001t0002g0012 a0001c0001t0002g0038 a0001c0001t0002g0197 others(8): Show |
14 | NA18612.hp1 NA18946.hp1 NA18953.hp2 others(11): Show |
intron_variant | MODIFIER | c.458+810G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 4/9 | chr13 | 49518961 | |||||||
| chr13:49518981 | G | A | 1 | a0001c0001t0002g0149 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.458+830G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 4/9 | chr13 | 49518981 | |||||||
| chr13:49518982 | C | T | 1 | a0001c0001t0002g0149 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.458+831C>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 4/9 | chr13 | 49518982 | |||||||
| chr13:49518983 | C | G | 1 | a0001c0001t0002g0149 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.458+832C>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 4/9 | chr13 | 49518983 | |||||||
| chr13:49518983 | C | T | 13 | a0001c0001t0001g0014 a0001c0001t0001g0033 a0001c0001t0001g0034 others(10): Show |
16 | HG02109.hp1 HG02257.hp1 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.458+832C>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 4/9 | chr13 | 49518983 | |||||||
| chr13:49518984 | C | T | 1 | a0001c0001t0002g0149 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.458+833C>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 4/9 | chr13 | 49518984 | |||||||
| chr13:49518987 | T | C | 45 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0015 others(42): Show |
53 | HG00733.hp1 HG01070.hp1 HG01109.hp1 others(50): Show |
intron_variant | MODIFIER | c.458+836T>C | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 4/9 | chr13 | 49518987 | |||||||
| chr13:49518990 | C | T | 4 | a0001c0001t0001g0072 a0001c0001t0001g0225 a0001c0001t0002g0149 others(1): Show |
4 | HG00733.hp1 HG01891.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.458+839C>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 4/9 | chr13 | 49518990 | |||||||
| chr13:49518992 | C | T | 1 | a0001c0001t0002g0149 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.458+841C>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 4/9 | chr13 | 49518992 | |||||||
| chr13:49518993 | G | A | 27 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0016 others(24): Show |
32 | HG01070.hp1 HG01109.hp1 HG01257.hp2 others(29): Show |
intron_variant | MODIFIER | c.458+842G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 4/9 | chr13 | 49518993 | |||||||
| chr13:49519051 | G | A | 1 | a0001c0001t0001g0113 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.458+900G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 4/9 | chr13 | 49519051 | |||||||
| chr13:49519057 | A | T | 2 | a0001c0001t0003g0256 a0001c0001t0003g0278 |
2 | HG03017.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.458+906A>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 4/9 | chr13 | 49519057 | |||||||
| chr13:49519062 | C | G | 11 | a0001c0001t0001g0133 a0001c0001t0001g0226 a0001c0001t0001g0240 others(8): Show |
13 | HG01106.hp1 HG01884.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.458+911C>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 4/9 | chr13 | 49519062 | |||||||
| chr13:49519078 | G | A | 2 | a0001c0001t0002g0159 a0001c0002t0002g0091 |
2 | HG01346.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.458+927G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 4/9 | chr13 | 49519078 | |||||||
| chr13:49519109 | A | G | 1 | a0001c0001t0001g0232 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.458+958A>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 4/9 | chr13 | 49519109 | |||||||
| chr13:49519169 | G | A | 4 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0112 others(1): Show |
4 | HG01109.hp2 HG02647.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.458+1018G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 4/9 | chr13 | 49519169 | |||||||
| chr13:49519169 | G | C | 1 | a0001c0001t0002g0191 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.458+1018G>C | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 4/9 | chr13 | 49519169 | |||||||
| chr13:49519191 | G | A | 6 | a0001c0001t0002g0007 a0001c0001t0002g0025 a0001c0001t0002g0026 others(3): Show |
10 | HG01975.hp1 HG02055.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.458+1040G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 4/9 | chr13 | 49519191 | |||||||
| chr13:49519307 | A | G | 1 | a0001c0001t0001g0072 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.458+1156A>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 4/9 | chr13 | 49519307 | |||||||
| chr13:49519316 | G | A | 124 | a0001c0001t0001g0158 a0001c0001t0001g0224 a0001c0001t0002g0001 others(121): Show |
161 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.458+1165G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 4/9 | chr13 | 49519316 | |||||||
| chr13:49519692 | C | CTTGAG | 279 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(276): Show |
341 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(338): Show |
intron_variant | MODIFIER | c.459-1201_459-1197d others(7): Show |
PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr13 | 49519692 | ||||||
| chr13:49519721 | T | C | 14 | a0001c0001t0001g0008 a0001c0001t0001g0100 a0001c0001t0001g0115 others(11): Show |
16 | HG00621.hp1 HG02165.hp1 HG02738.hp1 others(13): Show |
intron_variant | MODIFIER | c.459-1173T>C | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 4/9 | chr13 | 49519721 | |||||||
| chr13:49519757 | T | C | 2 | a0001c0001t0001g0286 a0001c0001t0001g0292 |
2 | HG02074.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.459-1137T>C | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 4/9 | chr13 | 49519757 | |||||||
| chr13:49519848 | G | A | 14 | a0001c0002t0001g0013 a0001c0002t0001g0039 a0001c0002t0001g0040 others(11): Show |
18 | HG00280.hp1 HG00639.hp2 HG00741.hp2 others(15): Show |
intron_variant | MODIFIER | c.459-1046G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 4/9 | chr13 | 49519848 | |||||||
| chr13:49519868 | A | G | 43 | a0001c0001t0002g0264 a0001c0001t0003g0004 a0001c0001t0003g0035 others(40): Show |
49 | HG00408.hp2 HG00558.hp2 HG00642.hp2 others(46): Show |
intron_variant | MODIFIER | c.459-1026A>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 4/9 | chr13 | 49519868 | |||||||
| chr13:49519869 | T | C | 1 | a0001c0001t0001g0058 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.459-1025T>C | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 4/9 | chr13 | 49519869 | |||||||
| chr13:49519886 | G | A | 9 | a0001c0001t0001g0133 a0001c0001t0002g0022 a0001c0001t0002g0023 others(6): Show |
11 | HG01106.hp1 HG02486.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.459-1008G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 4/9 | chr13 | 49519886 | |||||||
| chr13:49519954 | T | C | 42 | a0001c0001t0002g0264 a0001c0001t0003g0004 a0001c0001t0003g0035 others(39): Show |
48 | HG00408.hp2 HG00558.hp2 HG00642.hp2 others(45): Show |
intron_variant | MODIFIER | c.459-940T>C | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 4/9 | chr13 | 49519954 | |||||||
| chr13:49520037 | A | G | 2 | a0003c0006t0001g0066 a0003c0006t0001g0067 |
2 | HG02717.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.459-857A>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 4/9 | chr13 | 49520037 | |||||||
| chr13:49520046 | C | CT | 14 | a0001c0001t0001g0008 a0001c0001t0001g0100 a0001c0001t0001g0115 others(11): Show |
16 | HG00621.hp1 HG02165.hp1 HG02738.hp1 others(13): Show |
intron_variant | MODIFIER | c.459-844dupT | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr13 | 49520046 | ||||||
| chr13:49520051 | G | T | 241 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0014 others(238): Show |
297 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(294): Show |
intron_variant | MODIFIER | c.459-843G>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 4/9 | chr13 | 49520051 | |||||||
| chr13:49520087 | G | A | 1 | a0001c0001t0001g0224 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.459-807G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 4/9 | chr13 | 49520087 | |||||||
| chr13:49520112 | A | C | 1 | a0001c0001t0001g0072 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.459-782A>C | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 4/9 | chr13 | 49520112 | |||||||
| chr13:49520140 | C | T | 1 | a0001c0001t0001g0140 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.459-754C>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 4/9 | chr13 | 49520140 | |||||||
| chr13:49520152 | G | A | 4 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0112 others(1): Show |
4 | HG01109.hp2 HG02647.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.459-742G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 4/9 | chr13 | 49520152 | |||||||
| chr13:49520182 | G | A | 2 | a0001c0001t0002g0160 a0001c0001t0002g0190 |
2 | NA18969.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.459-712G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 4/9 | chr13 | 49520182 | |||||||
| chr13:49520185 | T | A | 269 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(266): Show |
330 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(327): Show |
intron_variant | MODIFIER | c.459-709T>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 4/9 | chr13 | 49520185 | |||||||
| chr13:49520236 | G | A | 269 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(266): Show |
330 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(327): Show |
intron_variant | MODIFIER | c.459-658G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 4/9 | chr13 | 49520236 | |||||||
| chr13:49520299 | G | A | 4 | a0001c0001t0001g0042 a0001c0001t0001g0109 a0001c0001t0001g0110 others(1): Show |
4 | HG02895.hp2 HG02897.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.459-595G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 4/9 | chr13 | 49520299 | |||||||
| chr13:49520367 | A | T | 1 | a0001c0001t0002g0108 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.459-527A>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 4/9 | chr13 | 49520367 | |||||||
| chr13:49520474 | T | G | 45 | a0001c0001t0002g0005 a0001c0001t0002g0012 a0001c0001t0002g0031 others(42): Show |
53 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(50): Show |
intron_variant | MODIFIER | c.459-420T>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 4/9 | chr13 | 49520474 | |||||||
| chr13:49520482 | A | C | 1 | a0001c0001t0003g0260 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.459-412A>C | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 4/9 | chr13 | 49520482 | |||||||
| chr13:49520557 | A | G | 1 | a0001c0002t0001g0081 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.459-337A>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 4/9 | chr13 | 49520557 | |||||||
| chr13:49520573 | A | C | 15 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0112 others(12): Show |
17 | HG01106.hp1 HG01109.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.459-321A>C | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 4/9 | chr13 | 49520573 | |||||||
| chr13:49520988 | T | C | 15 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0112 others(12): Show |
17 | HG01106.hp1 HG01109.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.505+48T>C | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 5/9 | chr13 | 49520988 | |||||||
| chr13:49520991 | A | G | 123 | a0001c0001t0001g0158 a0001c0001t0002g0001 a0001c0001t0002g0005 others(120): Show |
160 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(157): Show |
intron_variant | MODIFIER | c.505+51A>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 5/9 | chr13 | 49520991 | |||||||
| chr13:49521026 | G | A | 4 | a0001c0001t0001g0236 a0001c0001t0001g0242 a0001c0001t0001g0243 others(1): Show |
4 | HG01243.hp2 HG01884.hp1 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.505+86G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 5/9 | chr13 | 49521026 | |||||||
| chr13:49521078 | G | T | 1 | a0001c0001t0002g0148 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.505+138G>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 5/9 | chr13 | 49521078 | |||||||
| chr13:49521307 | A | G | 124 | a0001c0001t0001g0158 a0001c0001t0001g0224 a0001c0001t0002g0001 others(121): Show |
161 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.505+367A>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 5/9 | chr13 | 49521307 | |||||||
| chr13:49521546 | G | A | 4 | a0001c0001t0002g0204 a0001c0001t0002g0205 a0001c0001t0002g0206 others(1): Show |
4 | HG00735.hp2 HG03239.hp2 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.506-497G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 5/9 | chr13 | 49521546 | |||||||
| chr13:49521685 | G | A | 28 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0016 others(25): Show |
33 | HG01070.hp1 HG01109.hp1 HG01257.hp2 others(30): Show |
intron_variant | MODIFIER | c.506-358G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 5/9 | chr13 | 49521685 | |||||||
| chr13:49521817 | C | G | 173 | a0001c0001t0001g0158 a0001c0001t0001g0224 a0001c0001t0002g0001 others(170): Show |
216 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(213): Show |
intron_variant | MODIFIER | c.506-226C>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 5/9 | chr13 | 49521817 | |||||||
| chr13:49521822 | T | A | 1 | a0001c0001t0002g0179 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.506-221T>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 5/9 | chr13 | 49521822 | |||||||
| chr13:49521974 | T | C | 10 | a0001c0001t0001g0024 a0001c0001t0001g0138 a0001c0001t0001g0139 others(7): Show |
11 | HG01074.hp1 HG01243.hp1 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.506-69T>C | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 5/9 | chr13 | 49521974 | |||||||
| chr13:49521991 | C | G | 72 | a0001c0001t0001g0158 a0001c0001t0002g0001 a0001c0001t0002g0009 others(69): Show |
97 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.506-52C>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 5/9 | chr13 | 49521991 | |||||||
| chr13:49522148 | C | G | 1 | a0001c0001t0001g0245 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.570+41C>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 6/9 | chr13 | 49522148 | |||||||
| chr13:49522174 | A | G | 3 | a0001c0001t0002g0107 a0001c0001t0002g0108 a0001c0001t0002g0137 |
3 | HG02257.hp2 HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.570+67A>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 6/9 | chr13 | 49522174 | |||||||
| chr13:49522306 | A | G | 4 | a0001c0001t0001g0014 a0001c0001t0001g0043 a0001c0001t0001g0044 others(1): Show |
5 | HG02818.hp1 HG02922.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.570+199A>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 6/9 | chr13 | 49522306 | |||||||
| chr13:49522531 | C | T | 2 | a0001c0001t0002g0032 a0001c0001t0002g0223 |
3 | NA19004.hp2 NA19011.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.570+424C>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 6/9 | chr13 | 49522531 | |||||||
| chr13:49522564 | G | GATT | 279 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(276): Show |
341 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(338): Show |
intron_variant | MODIFIER | c.570+460_570+462dup others(3): Show |
PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr13 | 49522564 | ||||||
| chr13:49522581 | A | G | 1 | a0001c0001t0001g0052 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.570+474A>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 6/9 | chr13 | 49522581 | |||||||
| chr13:49522714 | A | G | 4 | a0001c0001t0001g0014 a0001c0001t0001g0043 a0001c0001t0001g0044 others(1): Show |
5 | HG02818.hp1 HG02922.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.571-461A>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 6/9 | chr13 | 49522714 | |||||||
| chr13:49522755 | TG | T | 41 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0068 others(38): Show |
49 | HG00544.hp2 HG00558.hp2 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.571-416delG | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr13 | 49522755 | ||||||
| chr13:49522758 | GGT | G | 19 | a0001c0001t0001g0003 a0001c0001t0001g0115 a0001c0001t0001g0116 others(16): Show |
25 | HG00099.hp2 HG00558.hp1 HG00642.hp1 others(22): Show |
intron_variant | MODIFIER | c.571-416_571-415del others(2): Show |
PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 6/9 | chr13 | 49522758 | |||||||
| chr13:49522758 | GGTT | G | 36 | a0001c0001t0001g0008 a0001c0001t0001g0100 a0001c0001t0001g0117 others(33): Show |
38 | HG00544.hp1 HG00621.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.571-416_571-414del others(3): Show |
PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 6/9 | chr13 | 49522758 | |||||||
| chr13:49522758 | GGTTT | G | 102 | a0001c0001t0001g0042 a0001c0001t0001g0072 a0001c0001t0001g0109 others(99): Show |
139 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.571-416_571-413del others(4): Show |
PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 6/9 | chr13 | 49522758 | |||||||
| chr13:49522758 | GGTTTT | G | 5 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0002g0161 others(2): Show |
5 | HG01496.hp2 HG02970.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.571-416_571-412del others(5): Show |
PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 6/9 | chr13 | 49522758 | |||||||
| chr13:49522759 | G | T | 21 | a0001c0001t0001g0238 a0001c0001t0001g0239 a0001c0001t0001g0246 others(18): Show |
21 | HG00408.hp2 HG02109.hp1 HG02257.hp2 others(18): Show |
intron_variant | MODIFIER | c.571-416G>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 6/9 | chr13 | 49522759 | |||||||
| chr13:49522763 | T | G | 2 | a0001c0001t0001g0069 a0001c0001t0001g0070 |
2 | HG01109.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.571-412T>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 6/9 | chr13 | 49522763 | |||||||
| chr13:49522765 | TTG | T | 22 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0016 others(19): Show |
27 | HG01070.hp1 HG01257.hp2 HG02015.hp2 others(24): Show |
intron_variant | MODIFIER | c.571-408_571-407del others(2): Show |
PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr13 | 49522765 | ||||||
| chr13:49522766 | TG | T | 15 | a0001c0001t0001g0049 a0001c0001t0001g0051 a0001c0001t0001g0055 others(12): Show |
16 | HG01109.hp1 HG01884.hp2 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.571-408delG | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 6/9 | chr13 | 49522766 | |||||||
| chr13:49522767 | G | T | 232 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0014 others(229): Show |
287 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(284): Show |
intron_variant | MODIFIER | c.571-408G>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 6/9 | chr13 | 49522767 | |||||||
| chr13:49522771 | T | G | 1 | a0001c0001t0001g0224 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.571-404T>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 6/9 | chr13 | 49522771 | |||||||
| chr13:49522807 | C | G | 4 | a0001c0001t0001g0042 a0001c0001t0001g0109 a0001c0001t0001g0110 others(1): Show |
4 | HG02895.hp2 HG02897.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.571-368C>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 6/9 | chr13 | 49522807 | |||||||
| chr13:49523487 | A | G | 8 | a0001c0001t0002g0208 a0001c0001t0002g0216 a0001c0001t0002g0217 others(5): Show |
8 | HG02074.hp1 NA18946.hp2 NA18957.hp1 others(5): Show |
intron_variant | MODIFIER | c.637+246A>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 7/9 | chr13 | 49523487 | |||||||
| chr13:49523491 | A | G | 1 | a0001c0001t0002g0213 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.637+250A>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 7/9 | chr13 | 49523491 | |||||||
| chr13:49523576 | T | C | 1 | a0001c0001t0001g0241 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.637+335T>C | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 7/9 | chr13 | 49523576 | |||||||
| chr13:49523623 | G | A | 3 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0001g0072 |
3 | HG02280.hp2 HG02818.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.637+382G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 7/9 | chr13 | 49523623 | |||||||
| chr13:49523626 | CTGT | C | 3 | a0001c0001t0002g0010 a0001c0001t0002g0164 a0001c0001t0002g0228 |
5 | HG00438.hp2 HG00544.hp1 NA18960.hp2 others(2): Show |
intron_variant | MODIFIER | c.637+387_637+389del others(3): Show |
PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 49523626 | ||||||
| chr13:49523754 | C | T | 42 | a0001c0001t0003g0004 a0001c0001t0003g0035 a0001c0001t0003g0036 others(39): Show |
48 | HG00558.hp2 HG00642.hp2 HG01255.hp2 others(45): Show |
intron_variant | MODIFIER | c.638-331C>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 7/9 | chr13 | 49523754 | |||||||
| chr13:49523843 | T | C | 137 | a0001c0001t0001g0024 a0001c0001t0001g0138 a0001c0001t0001g0139 others(134): Show |
175 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.638-242T>C | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 7/9 | chr13 | 49523843 | |||||||
| chr13:49523870 | T | C | 2 | a0001c0002t0001g0095 a0001c0002t0001g0096 |
2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.638-215T>C | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 7/9 | chr13 | 49523870 | |||||||
| chr13:49523919 | A | G | 4 | a0001c0001t0001g0042 a0001c0001t0001g0109 a0001c0001t0001g0110 others(1): Show |
4 | HG02895.hp2 HG02897.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.638-166A>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 7/9 | chr13 | 49523919 | |||||||
| chr13:49523930 | T | A | 1 | a0001c0001t0002g0202 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.638-155T>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 7/9 | chr13 | 49523930 | |||||||
| chr13:49524240 | G | A | 1 | a0001c0001t0002g0264 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.769+24G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 8/9 | chr13 | 49524240 | |||||||
| chr13:49524240 | G | T | 88 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0016 others(85): Show |
103 | HG00558.hp2 HG00642.hp2 HG01070.hp1 others(100): Show |
intron_variant | MODIFIER | c.769+24G>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 8/9 | chr13 | 49524240 | |||||||
| chr13:49524271 | TAAAAC | T | 130 | a0001c0001t0001g0224 a0001c0001t0002g0001 a0001c0001t0002g0005 others(127): Show |
167 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.769+64_769+68delAC others(3): Show |
PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr13 | 49524271 | ||||||
| chr13:49524305 | C | T | 1 | a0001c0001t0001g0048 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.769+89C>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 8/9 | chr13 | 49524305 | |||||||
| chr13:49524477 | C | CT | 13 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0068 others(10): Show |
15 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.769+275dupT | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr13 | 49524477 | ||||||
| chr13:49524477 | CT | C | 38 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0043 others(35): Show |
45 | HG00544.hp2 HG00558.hp1 HG00597.hp2 others(42): Show |
intron_variant | MODIFIER | c.769+275delT | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr13 | 49524477 | ||||||
| chr13:49524497 | G | A | 20 | a0001c0001t0001g0008 a0001c0001t0001g0024 a0001c0001t0001g0100 others(17): Show |
23 | HG00621.hp1 HG01074.hp1 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.769+281G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 8/9 | chr13 | 49524497 | |||||||
| chr13:49524567 | C | T | 130 | a0001c0001t0001g0224 a0001c0001t0002g0001 a0001c0001t0002g0005 others(127): Show |
167 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.769+351C>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 8/9 | chr13 | 49524567 | |||||||
| chr13:49524568 | A | G | 131 | a0001c0001t0001g0224 a0001c0001t0002g0001 a0001c0001t0002g0005 others(128): Show |
168 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.769+352A>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 8/9 | chr13 | 49524568 | |||||||
| chr13:49524727 | C | T | 1 | a0001c0001t0002g0056 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.769+511C>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 8/9 | chr13 | 49524727 | |||||||
| chr13:49524755 | C | A | 1 | a0001c0001t0001g0043 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.769+539C>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 8/9 | chr13 | 49524755 | |||||||
| chr13:49524766 | A | G | 129 | a0001c0001t0001g0224 a0001c0001t0002g0001 a0001c0001t0002g0005 others(126): Show |
166 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.769+550A>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 8/9 | chr13 | 49524766 | |||||||
| chr13:49524791 | T | G | 3 | a0001c0001t0002g0204 a0001c0001t0002g0205 a0001c0001t0002g0206 |
3 | HG00735.hp2 HG04184.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.769+575T>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 8/9 | chr13 | 49524791 | |||||||
| chr13:49524830 | T | C | 130 | a0001c0001t0001g0224 a0001c0001t0002g0001 a0001c0001t0002g0005 others(127): Show |
167 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.769+614T>C | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 8/9 | chr13 | 49524830 | |||||||
| chr13:49524870 | C | G | 1 | a0001c0001t0003g0281 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.769+654C>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 8/9 | chr13 | 49524870 | |||||||
| chr13:49524965 | G | A | 1 | a0001c0002t0001g0083 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.769+749G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 8/9 | chr13 | 49524965 | |||||||
| chr13:49525021 | A | C | 15 | a0001c0002t0001g0011 a0001c0002t0001g0013 a0001c0002t0001g0039 others(12): Show |
21 | HG00280.hp1 HG00639.hp2 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.769+805A>C | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 8/9 | chr13 | 49525021 | |||||||
| chr13:49525052 | C | A | 220 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0024 others(217): Show |
272 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(269): Show |
intron_variant | MODIFIER | c.769+836C>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 8/9 | chr13 | 49525052 | |||||||
| chr13:49525192 | G | A | 130 | a0001c0001t0001g0224 a0001c0001t0002g0001 a0001c0001t0002g0005 others(127): Show |
167 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.769+976G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 8/9 | chr13 | 49525192 | |||||||
| chr13:49525303 | A | C | 90 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0024 others(87): Show |
105 | HG00544.hp2 HG00558.hp1 HG00558.hp2 others(102): Show |
intron_variant | MODIFIER | c.770-1084A>C | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 8/9 | chr13 | 49525303 | |||||||
| chr13:49525404 | C | T | 130 | a0001c0001t0001g0224 a0001c0001t0002g0001 a0001c0001t0002g0005 others(127): Show |
167 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.770-983C>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 8/9 | chr13 | 49525404 | |||||||
| chr13:49525439 | A | G | 1 | a0001c0001t0002g0150 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.770-948A>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 8/9 | chr13 | 49525439 | |||||||
| chr13:49525595 | TTATAAA | T | 4 | a0001c0001t0001g0236 a0001c0001t0001g0242 a0001c0001t0001g0243 others(1): Show |
4 | HG01243.hp2 HG01884.hp1 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.770-787_770-782del others(6): Show |
PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr13 | 49525595 | ||||||
| chr13:49525603 | A | G | 6 | a0001c0001t0001g0024 a0001c0001t0001g0138 a0001c0001t0001g0139 others(3): Show |
7 | HG01074.hp1 HG01243.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.770-784A>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 8/9 | chr13 | 49525603 | |||||||
| chr13:49525644 | G | A | 1 | a0001c0001t0001g0238 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.770-743G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 8/9 | chr13 | 49525644 | |||||||
| chr13:49525954 | T | A | 125 | a0001c0001t0001g0224 a0001c0001t0002g0001 a0001c0001t0002g0005 others(122): Show |
162 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(159): Show |
intron_variant | MODIFIER | c.770-433T>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 8/9 | chr13 | 49525954 | |||||||
| chr13:49525960 | G | A | 1 | a0001c0001t0001g0118 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.770-427G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 8/9 | chr13 | 49525960 | |||||||
| chr13:49525979 | GCC | G | 6 | a0001c0001t0001g0024 a0001c0001t0001g0138 a0001c0001t0001g0139 others(3): Show |
7 | HG01074.hp1 HG01243.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.770-407_770-406del others(2): Show |
PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 8/9 | chr13 | 49525979 | |||||||
| chr13:49526168 | CA | C | 37 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0015 others(34): Show |
43 | HG01070.hp1 HG01070.hp2 HG01109.hp1 others(40): Show |
intron_variant | MODIFIER | c.770-197delA | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr13 | 49526168 | ||||||
| chr13:49526168 | CAA | C | 68 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0042 others(65): Show |
78 | HG00558.hp2 HG00642.hp2 HG01106.hp1 others(75): Show |
intron_variant | MODIFIER | c.770-198_770-197del others(2): Show |
PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr13 | 49526168 | ||||||
| chr13:49526168 | CAAA | C | 42 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0024 others(39): Show |
51 | HG00544.hp2 HG00558.hp1 HG00597.hp2 others(48): Show |
intron_variant | MODIFIER | c.770-199_770-197del others(3): Show |
PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr13 | 49526168 | ||||||
| chr13:49526168 | CAAAA | C | 130 | a0001c0001t0001g0224 a0001c0001t0002g0001 a0001c0001t0002g0005 others(127): Show |
167 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.770-200_770-197del others(4): Show |
PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr13 | 49526168 | ||||||
| chr13:49526184 | A | G | 132 | a0001c0001t0001g0224 a0001c0001t0001g0226 a0001c0001t0001g0240 others(129): Show |
169 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.770-203A>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 8/9 | chr13 | 49526184 | |||||||
| chr13:49526185 | A | G | 5 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0112 others(2): Show |
5 | HG01109.hp2 HG01978.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.770-202A>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 8/9 | chr13 | 49526185 | |||||||
| chr13:49526191 | G | A | 1 | a0001c0002t0001g0075 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.770-196G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 8/9 | chr13 | 49526191 | |||||||
| chr13:49526192 | A | G | 1 | a0001c0002t0001g0075 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.770-195A>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 8/9 | chr13 | 49526192 | |||||||
| chr13:49526253 | T | C | 130 | a0001c0001t0001g0224 a0001c0001t0002g0001 a0001c0001t0002g0005 others(127): Show |
167 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.770-134T>C | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 8/9 | chr13 | 49526253 | |||||||
| chr13:49526325 | T | C | 4 | a0001c0001t0001g0014 a0001c0001t0001g0043 a0001c0001t0001g0044 others(1): Show |
5 | HG02818.hp1 HG02922.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.770-62T>C | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 8/9 | chr13 | 49526325 | |||||||
| chr13:49526487 | C | T | 12 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0068 others(9): Show |
14 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.841+29C>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 9/9 | chr13 | 49526487 | |||||||
| chr13:49526491 | GTT | G | 130 | a0001c0001t0001g0224 a0001c0001t0002g0001 a0001c0001t0002g0005 others(127): Show |
167 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.841+36_841+37delTT | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr13 | 49526491 | ||||||
| chr13:49526501 | ATATT | A | 130 | a0001c0001t0001g0224 a0001c0001t0002g0001 a0001c0001t0002g0005 others(127): Show |
167 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.841+47_841+50delTT others(2): Show |
PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr13 | 49526501 | ||||||
| chr13:49526511 | C | T | 130 | a0001c0001t0001g0224 a0001c0001t0002g0001 a0001c0001t0002g0005 others(127): Show |
167 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.841+53C>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 9/9 | chr13 | 49526511 | |||||||
| chr13:49526531 | G | A | 130 | a0001c0001t0001g0224 a0001c0001t0002g0001 a0001c0001t0002g0005 others(127): Show |
167 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.841+73G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 9/9 | chr13 | 49526531 | |||||||
| chr13:49526532 | T | C | 14 | a0001c0001t0001g0008 a0001c0001t0001g0100 a0001c0001t0001g0115 others(11): Show |
16 | HG00621.hp1 HG02165.hp1 HG02738.hp1 others(13): Show |
intron_variant | MODIFIER | c.841+74T>C | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 9/9 | chr13 | 49526532 | |||||||
| chr13:49526620 | T | C | 140 | a0001c0001t0001g0224 a0001c0001t0002g0001 a0001c0001t0002g0005 others(137): Show |
179 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.841+162T>C | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 9/9 | chr13 | 49526620 | |||||||
| chr13:49526621 | G | C | 140 | a0001c0001t0001g0224 a0001c0001t0002g0001 a0001c0001t0002g0005 others(137): Show |
179 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.841+163G>C | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 9/9 | chr13 | 49526621 | |||||||
| chr13:49526646 | C | T | 140 | a0001c0001t0001g0224 a0001c0001t0002g0001 a0001c0001t0002g0005 others(137): Show |
179 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.841+188C>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 9/9 | chr13 | 49526646 | |||||||
| chr13:49526702 | G | T | 6 | a0001c0001t0001g0024 a0001c0001t0001g0138 a0001c0001t0001g0139 others(3): Show |
7 | HG01074.hp1 HG01243.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.841+244G>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 9/9 | chr13 | 49526702 | |||||||
| chr13:49526762 | A | G | 135 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0007 others(132): Show |
174 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.841+304A>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 9/9 | chr13 | 49526762 | |||||||
| chr13:49526799 | T | C | 3 | a0001c0001t0002g0208 a0001c0001t0002g0211 a0001c0001t0002g0222 |
3 | HG00438.hp1 NA19011.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.841+341T>C | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 9/9 | chr13 | 49526799 | |||||||
| chr13:49526937 | C | T | 140 | a0001c0001t0001g0224 a0001c0001t0002g0001 a0001c0001t0002g0005 others(137): Show |
179 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.841+479C>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 9/9 | chr13 | 49526937 | |||||||
| chr13:49526958 | G | A | 140 | a0001c0001t0001g0224 a0001c0001t0002g0001 a0001c0001t0002g0005 others(137): Show |
179 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.841+500G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 9/9 | chr13 | 49526958 | |||||||
| chr13:49527010 | T | C | 1 | a0001c0002t0001g0087 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.841+552T>C | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 9/9 | chr13 | 49527010 | |||||||
| chr13:49527023 | G | A | 140 | a0001c0001t0001g0224 a0001c0001t0002g0001 a0001c0001t0002g0005 others(137): Show |
179 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.841+565G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 9/9 | chr13 | 49527023 | |||||||
| chr13:49527028 | G | C | 8 | a0001c0002t0001g0018 a0001c0002t0001g0021 a0001c0002t0001g0074 others(5): Show |
10 | HG02040.hp1 NA18943.hp1 NA18961.hp1 others(7): Show |
intron_variant | MODIFIER | c.841+570G>C | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 9/9 | chr13 | 49527028 | |||||||
| chr13:49527033 | C | T | 15 | a0001c0001t0001g0008 a0001c0001t0001g0100 a0001c0001t0001g0115 others(12): Show |
19 | HG00621.hp1 HG02165.hp1 HG02615.hp2 others(16): Show |
intron_variant | MODIFIER | c.841+575C>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 9/9 | chr13 | 49527033 | |||||||
| chr13:49527054 | GA | G | 45 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0024 others(42): Show |
56 | HG00544.hp2 HG00597.hp2 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.841+608delA | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr13 | 49527054 | ||||||
| chr13:49527060 | A | AAAC | 136 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0007 others(133): Show |
175 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.841+604_841+605ins others(3): Show |
PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr13 | 49527060 | ||||||
| chr13:49527066 | AC | A | 43 | a0001c0001t0003g0004 a0001c0001t0003g0035 a0001c0001t0003g0036 others(40): Show |
49 | HG00558.hp1 HG00558.hp2 HG00642.hp2 others(46): Show |
intron_variant | MODIFIER | c.841+609delC | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 9/9 | chr13 | 49527066 | |||||||
| chr13:49527067 | C | A | 1 | a0001c0001t0002g0168 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.841+609C>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 9/9 | chr13 | 49527067 | |||||||
| chr13:49527068 | A | C | 1 | a0001c0001t0002g0168 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.841+610A>C | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 9/9 | chr13 | 49527068 | |||||||
| chr13:49527080 | AC | A | 140 | a0001c0001t0001g0224 a0001c0001t0002g0001 a0001c0001t0002g0005 others(137): Show |
179 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.841+623delC | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 9/9 | chr13 | 49527080 | |||||||
| chr13:49527390 | C | T | 115 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0007 others(112): Show |
154 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(151): Show |
intron_variant | MODIFIER | c.841+932C>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 9/9 | chr13 | 49527390 | |||||||
| chr13:49527518 | A | T | 139 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0007 others(136): Show |
178 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(175): Show |
intron_variant | MODIFIER | c.842-993A>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 9/9 | chr13 | 49527518 | |||||||
| chr13:49527527 | C | T | 5 | a0001c0001t0001g0014 a0001c0001t0001g0043 a0001c0001t0001g0044 others(2): Show |
6 | HG02818.hp1 HG02922.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.842-984C>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 9/9 | chr13 | 49527527 | |||||||
| chr13:49527927 | T | G | 139 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0007 others(136): Show |
178 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(175): Show |
intron_variant | MODIFIER | c.842-584T>G | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 9/9 | chr13 | 49527927 | |||||||
| chr13:49527940 | G | GTGTTT | 139 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0007 others(136): Show |
178 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(175): Show |
intron_variant | MODIFIER | c.842-570_842-569ins others(5): Show |
PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr13 | 49527940 | ||||||
| chr13:49527995 | T | C | 16 | a0001c0001t0001g0014 a0001c0001t0001g0033 a0001c0001t0001g0034 others(13): Show |
19 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.842-516T>C | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 9/9 | chr13 | 49527995 | |||||||
| chr13:49528083 | C | T | 226 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0024 others(223): Show |
282 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(279): Show |
intron_variant | MODIFIER | c.842-428C>T | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 9/9 | chr13 | 49528083 | |||||||
| chr13:49528121 | G | A | 1 | a0001c0001t0001g0238 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.842-390G>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 9/9 | chr13 | 49528121 | |||||||
| chr13:49528236 | T | A | 139 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0007 others(136): Show |
178 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(175): Show |
intron_variant | MODIFIER | c.842-275T>A | PHF11 | ENSG00000136147.18 | transcript | ENST00000378319.8 | protein_coding | 9/9 | chr13 | 49528236 |