Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 54969 |
| ensemblid | ENSG00000056050.7 |
| hgncid | 26051 |
| symbol | HPF1 |
| name | histone PARylation factor 1 |
| refseq_nuc | NM_017867.3 |
| refseq_prot | NP_060337.2 |
| ensembl_nuc | ENST00000393381.3 |
| ensembl_prot | ENSP00000406598.1 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 169729470 |
| end | 169757944 |
| strand | - |
| ver | v1.2 |
| region | chr4:169729470-169757944 |
| region5000 | chr4:169724470-169762944 |
| regionname0 | HPF1_chr4_169729470_169757944 |
| regionname5000 | HPF1_chr4_169724470_169762944 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 346 | 226 | 64 | 41 | 89 | 6 | 26 | 63 | HPF1_chr4_169724470_169762944 | HPF1 | MVGGG others(341): Show |
chr4 | 169724470 | 169762944 |
| a0002 | 1/0 | 346 | 90 | 30 | 11 | 29 | 4 | 15 | 25 | HPF1_chr4_169724470_169762944 | HPF1 | MVGGG others(341): Show |
chr4 | 169724470 | 169762944 |
| a0003 | 0/0 | 346 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | MVGGG others(341): Show |
chr4 | 169724470 | 169762944 |
| a0004 | 0/0 | 81 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | MVGGG others(76): Show |
chr4 | 169724470 | 169762944 |
| a0005 | 0/1 | 346 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | MVGGG others(341): Show |
chr4 | 169724470 | 169762944 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1038 | 188 | 38 | 39 | 81 | 6 | 24 | HPF1_chr4_169724470_169762944 | HPF1 | ATGGT others(1033): Show |
chr4 | 169724470 | 169762944 | ||
| a0001c0004 | 0/0 | 1038 | 33 | 21 | 2 | 8 | 0 | 2 | HPF1_chr4_169724470_169762944 | HPF1 | ATGGT others(1033): Show |
chr4 | 169724470 | 169762944 | ||
| a0001c0005 | 0/0 | 1038 | 5 | 5 | 0 | 0 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | ATGGT others(1033): Show |
chr4 | 169724470 | 169762944 | ||
| a0002c0002 | 1/0 | 1038 | 55 | 9 | 8 | 25 | 3 | 9 | HPF1_chr4_169724470_169762944 | HPF1 | ATGGT others(1033): Show |
chr4 | 169724470 | 169762944 | ||
| a0002c0003 | 0/0 | 1038 | 34 | 20 | 3 | 4 | 1 | 6 | HPF1_chr4_169724470_169762944 | HPF1 | ATGGT others(1033): Show |
chr4 | 169724470 | 169762944 | ||
| a0002c0009 | 0/0 | 1038 | 1 | 1 | 0 | 0 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | ATGGT others(1033): Show |
chr4 | 169724470 | 169762944 | ||
| a0003c0006 | 0/0 | 1038 | 2 | 2 | 0 | 0 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | ATGGT others(1033): Show |
chr4 | 169724470 | 169762944 | ||
| a0004c0008 | 0/0 | 848 | 1 | 0 | 0 | 0 | 0 | 1 | HPF1_chr4_169724470_169762944 | HPF1 | ATGGT others(843): Show |
chr4 | 169724470 | 169762944 | ||
| a0005c0007 | 0/1 | 1038 | 1 | 0 | 0 | 0 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | ATGGT others(1033): Show |
chr4 | 169724470 | 169762944 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 1216 | 180 | 35 | 36 | 81 | 5 | 23 | HPF1_chr4_169724470_169762944 | HPF1 | GGAAG others(1211): Show |
chr4 | 169724470 | 169762944 |
| a0001c0001t0002 | 0/0 | 1214 | 6 | 3 | 2 | 0 | 1 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | GGAAG others(1209): Show |
chr4 | 169724470 | 169762944 |
| a0001c0001t0003 | 0/0 | 1216 | 1 | 0 | 1 | 0 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | GGAAG others(1211): Show |
chr4 | 169724470 | 169762944 |
| a0001c0001t0004 | 0/0 | 1216 | 1 | 0 | 0 | 0 | 0 | 1 | HPF1_chr4_169724470_169762944 | HPF1 | GGAAG others(1211): Show |
chr4 | 169724470 | 169762944 |
| a0001c0004t0001 | 0/0 | 1216 | 21 | 17 | 1 | 1 | 0 | 2 | HPF1_chr4_169724470_169762944 | HPF1 | GGAAG others(1211): Show |
chr4 | 169724470 | 169762944 |
| a0001c0004t0002 | 0/0 | 1214 | 12 | 4 | 1 | 7 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | GGAAG others(1209): Show |
chr4 | 169724470 | 169762944 |
| a0001c0005t0001 | 0/0 | 1216 | 5 | 5 | 0 | 0 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | GGAAG others(1211): Show |
chr4 | 169724470 | 169762944 |
| a0002c0002t0001 | 1/0 | 1216 | 54 | 8 | 8 | 25 | 3 | 9 | HPF1_chr4_169724470_169762944 | HPF1 | GGAAG others(1211): Show |
chr4 | 169724470 | 169762944 |
| a0002c0002t0002 | 0/0 | 1214 | 1 | 1 | 0 | 0 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | GGAAG others(1209): Show |
chr4 | 169724470 | 169762944 |
| a0002c0003t0001 | 0/0 | 1216 | 31 | 17 | 3 | 4 | 1 | 6 | HPF1_chr4_169724470_169762944 | HPF1 | GGAAG others(1211): Show |
chr4 | 169724470 | 169762944 |
| a0002c0003t0002 | 0/0 | 1214 | 3 | 3 | 0 | 0 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | GGAAG others(1209): Show |
chr4 | 169724470 | 169762944 |
| a0002c0009t0001 | 0/0 | 1216 | 1 | 1 | 0 | 0 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | GGAAG others(1211): Show |
chr4 | 169724470 | 169762944 |
| a0003c0006t0001 | 0/0 | 1216 | 2 | 2 | 0 | 0 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | GGAAG others(1211): Show |
chr4 | 169724470 | 169762944 |
| a0004c0008t0001 | 0/0 | 1026 | 1 | 0 | 0 | 0 | 0 | 1 | HPF1_chr4_169724470_169762944 | HPF1 | GGAAG others(1021): Show |
chr4 | 169724470 | 169762944 |
| a0005c0007t0001 | 0/1 | 1216 | 1 | 0 | 0 | 0 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | GGAAG others(1211): Show |
chr4 | 169724470 | 169762944 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 29 | 1 | 6 | 19 | 1 | 2 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0001t0001g0003 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0001t0001g0004 | 0/0 | 7 | 6 | 1 | 0 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0001t0001g0005 | 0/0 | 6 | 1 | 1 | 4 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0001t0001g0006 | 0/0 | 6 | 0 | 2 | 3 | 0 | 1 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0001t0001g0007 | 0/0 | 5 | 0 | 2 | 0 | 1 | 2 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0001t0001g0008 | 0/0 | 4 | 0 | 1 | 2 | 0 | 1 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0001t0001g0012 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0001t0001g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0001t0001g0026 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0001t0001g0030 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0001t0001g0031 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0001t0002g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0001t0002g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0001t0002g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0001t0003g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0001t0004g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0004t0001g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0004t0001g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0004t0001g0020 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0004t0001g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0004t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0004t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0004t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0004t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0004t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0004t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0004t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0004t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0004t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0004t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0004t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0004t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0004t0002g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0004t0002g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0004t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0004t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0004t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0004t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0004t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0004t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0004t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0004t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0005t0001g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0005t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0005t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0001c0005t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0002c0002t0001g0002 | 0/0 | 22 | 0 | 6 | 12 | 1 | 3 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0002c0002t0001g0009 | 0/0 | 3 | 0 | 0 | 1 | 1 | 1 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0002c0002t0001g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0002c0002t0001g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0002c0002t0001g0016 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0002c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0002c0002t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0002c0002t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0002c0002t0001g0040 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0002c0002t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0002c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0002c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0002c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0002c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0002c0002t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0002c0002t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0002c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0002c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0002c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0002c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0002c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0002c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0002c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0002c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0002c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0002c0002t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0002c0002t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0002c0002t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0002c0002t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0002c0003t0001g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0002c0003t0001g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0002c0003t0001g0023 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0002c0003t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0002c0003t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0002c0003t0001g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0002c0003t0001g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0002c0003t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0002c0003t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0002c0003t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0002c0003t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0002c0003t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0002c0003t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0002c0003t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0002c0003t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0002c0003t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0002c0003t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0002c0003t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0002c0003t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0002c0003t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0002c0003t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0002c0003t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0002c0003t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0002c0003t0002g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0002c0003t0002g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0002c0003t0002g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0002c0009t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0003c0006t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0003c0006t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0004c0008t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| a0005c0007t0001g0101 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0173 | EUR | GBR | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0171 | EUR | GBR | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG00140 | hp1 | a0002 | c0003 | t0001 | g0131 | EUR | GBR | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0026 | EUR | GBR | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0178 | EUR | FIN | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG00280 | hp2 | a0002 | c0002 | t0001 | g0009 | EUR | FIN | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | CHS | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | CHS | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG00558 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | CHS | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | CHS | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG00621 | hp2 | a0002 | c0002 | t0001 | g0044 | EAS | CHS | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | PUR | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0170 | AMR | PUR | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG01074 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0185 | AMR | PUR | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | PUR | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG01106 | hp1 | a0002 | c0003 | t0001 | g0027 | AMR | PUR | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG01109 | hp1 | a0001 | c0004 | t0001 | g0020 | AMR | PUR | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG01109 | hp2 | a0002 | c0003 | t0001 | g0023 | AMR | PUR | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0176 | AMR | PUR | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG01168 | hp2 | a0001 | c0001 | t0003 | g0146 | AMR | PUR | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0155 | AMR | PUR | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG01192 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG01243 | hp1 | a0002 | c0002 | t0001 | g0047 | AMR | PUR | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | PUR | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG01257 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | CLM | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG01258 | hp2 | a0002 | c0002 | t0001 | g0046 | AMR | CLM | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG01261 | hp1 | a0002 | c0003 | t0001 | g0027 | AMR | CLM | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | CLM | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | CLM | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0192 | AMR | CLM | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | CLM | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | CLM | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | CLM | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | CLM | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0007 | EUR | IBS | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG01517 | hp2 | a0002 | c0002 | t0001 | g0002 | EUR | IBS | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG01884 | hp1 | a0001 | c0004 | t0001 | g0010 | AFR | ACB | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0193 | AFR | ACB | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG01891 | hp2 | a0002 | c0003 | t0002 | g0202 | AFR | ACB | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG01978 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | PEL | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | PEL | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG01981 | hp1 | a0001 | c0004 | t0002 | g0065 | AMR | PEL | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG01981 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PEL | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0174 | AMR | PEL | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0159 | AMR | PEL | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | PEL | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0166 | AMR | PEL | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | KHV | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG02040 | hp1 | a0002 | c0002 | t0001 | g0042 | EAS | KHV | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | KHV | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | ACB | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG02055 | hp2 | a0002 | c0003 | t0001 | g0089 | AFR | ACB | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | KHV | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG02080 | hp1 | a0001 | c0004 | t0001 | g0036 | EAS | KHV | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG02132 | hp2 | a0001 | c0004 | t0002 | g0067 | EAS | KHV | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | KHV | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | KHV | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | ACB | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG02155 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | CDX | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG02258 | hp1 | a0002 | c0002 | t0001 | g0078 | AFR | ACB | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG02258 | hp2 | a0002 | c0003 | t0001 | g0091 | AFR | ACB | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG02273 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | PEL | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | PEL | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0205 | AFR | ACB | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | ACB | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG02451 | hp1 | a0001 | c0004 | t0002 | g0018 | AFR | ACB | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | ACB | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | KHV | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG02572 | hp1 | a0001 | c0004 | t0001 | g0073 | AFR | GWD | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG02572 | hp2 | a0001 | c0005 | t0001 | g0208 | AFR | GWD | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0167 | SAS | PJL | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG02602 | hp2 | a0001 | c0004 | t0001 | g0061 | SAS | PJL | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG02615 | hp1 | a0001 | c0004 | t0001 | g0060 | AFR | GWD | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG02615 | hp2 | a0001 | c0004 | t0001 | g0076 | AFR | GWD | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG02622 | hp1 | a0002 | c0003 | t0001 | g0098 | AFR | GWD | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | GWD | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG02630 | hp1 | a0001 | c0004 | t0001 | g0075 | AFR | GWD | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | GWD | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG02647 | hp2 | a0002 | c0003 | t0001 | g0097 | AFR | GWD | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0134 | SAS | PJL | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | GWD | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0099 | AFR | GWD | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG02723 | hp1 | a0002 | c0002 | t0002 | g0057 | AFR | GWD | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0204 | AFR | GWD | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0187 | SAS | PJL | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG02735 | hp2 | a0002 | c0003 | t0001 | g0093 | SAS | PJL | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG02809 | hp1 | a0002 | c0003 | t0001 | g0096 | AFR | GWD | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG02809 | hp2 | a0002 | c0003 | t0001 | g0196 | AFR | GWD | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG02818 | hp1 | a0001 | c0004 | t0001 | g0019 | AFR | GWD | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG02818 | hp2 | a0002 | c0002 | t0001 | g0014 | AFR | GWD | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG02886 | hp1 | a0001 | c0004 | t0001 | g0072 | AFR | GWD | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG02886 | hp2 | a0003 | c0006 | t0001 | g0084 | AFR | GWD | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG02895 | hp1 | a0001 | c0004 | t0001 | g0058 | AFR | GWD | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG02895 | hp2 | a0002 | c0002 | t0001 | g0039 | AFR | GWD | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | GWD | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG02896 | hp2 | a0002 | c0003 | t0001 | g0025 | AFR | GWD | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG02897 | hp1 | a0002 | c0003 | t0001 | g0025 | AFR | GWD | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG02897 | hp2 | a0001 | c0004 | t0001 | g0056 | AFR | GWD | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG02922 | hp1 | a0001 | c0004 | t0001 | g0021 | AFR | ESN | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG02922 | hp2 | a0001 | c0004 | t0001 | g0010 | AFR | ESN | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG02970 | hp1 | a0002 | c0003 | t0002 | g0085 | AFR | ESN | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | ESN | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG02976 | hp1 | a0001 | c0004 | t0002 | g0063 | AFR | ESN | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | ESN | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0107 | SAS | PJL | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0203 | AFR | GWD | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG03098 | hp2 | a0002 | c0003 | t0001 | g0022 | AFR | MSL | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG03130 | hp1 | a0001 | c0004 | t0002 | g0069 | AFR | ESN | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG03130 | hp2 | a0002 | c0003 | t0002 | g0201 | AFR | ESN | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG03139 | hp1 | a0002 | c0003 | t0001 | g0080 | AFR | ESN | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG03195 | hp1 | a0002 | c0003 | t0001 | g0024 | AFR | ESN | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0199 | AFR | ESN | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0198 | AFR | MSL | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG03225 | hp1 | a0002 | c0003 | t0001 | g0024 | AFR | MSL | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG03225 | hp2 | a0002 | c0002 | t0001 | g0015 | AFR | MSL | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG03453 | hp1 | a0002 | c0003 | t0001 | g0023 | AFR | MSL | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | MSL | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG03486 | hp1 | a0002 | c0002 | t0001 | g0071 | AFR | MSL | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | MSL | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG03490 | hp1 | a0002 | c0002 | t0001 | g0002 | SAS | PJL | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG03491 | hp1 | a0002 | c0002 | t0001 | g0053 | SAS | PJL | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0145 | SAS | PJL | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG03492 | hp1 | a0002 | c0002 | t0001 | g0002 | SAS | PJL | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG03492 | hp2 | a0002 | c0002 | t0001 | g0016 | SAS | PJL | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | ESN | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG03516 | hp2 | a0002 | c0003 | t0001 | g0086 | AFR | ESN | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG03540 | hp1 | a0001 | c0005 | t0001 | g0207 | AFR | GWD | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG03540 | hp2 | a0002 | c0009 | t0001 | g0209 | AFR | GWD | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | MSL | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | MSL | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG03654 | hp1 | a0002 | c0002 | t0001 | g0045 | SAS | PJL | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG03654 | hp2 | a0001 | c0004 | t0001 | g0020 | SAS | PJL | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0175 | SAS | PJL | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0115 | SAS | PJL | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0110 | SAS | STU | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0114 | SAS | STU | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0112 | SAS | PJL | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG03704 | hp2 | a0002 | c0003 | t0001 | g0163 | SAS | PJL | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG03710 | hp1 | a0002 | c0002 | t0001 | g0009 | SAS | PJL | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0012 | SAS | BEB | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG03831 | hp2 | a0002 | c0002 | t0001 | g0002 | SAS | BEB | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0028 | SAS | BEB | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG03927 | hp1 | a0002 | c0003 | t0001 | g0092 | SAS | BEB | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG03927 | hp2 | a0004 | c0008 | t0001 | g0108 | SAS | BEB | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG03942 | hp1 | a0001 | c0001 | t0004 | g0168 | SAS | BEB | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0169 | SAS | BEB | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0012 | SAS | STU | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG04115 | hp2 | a0002 | c0003 | t0001 | g0164 | SAS | STU | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG04184 | hp1 | a0002 | c0003 | t0001 | g0094 | SAS | BEB | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | BEB | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG04204 | hp1 | a0002 | c0003 | t0001 | g0162 | SAS | STU | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0129 | SAS | STU | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG04228 | hp2 | a0002 | c0002 | t0001 | g0064 | SAS | STU | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | YRI | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| NA18522 | hp2 | a0001 | c0004 | t0001 | g0019 | AFR | YRI | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHB | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | CHB | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHB | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| NA18906 | hp1 | a0001 | c0004 | t0001 | g0010 | AFR | YRI | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| NA18906 | hp2 | a0001 | c0005 | t0001 | g0035 | AFR | YRI | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| NA18939 | hp2 | a0002 | c0003 | t0001 | g0011 | EAS | JPT | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| NA18943 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| NA18950 | hp1 | a0002 | c0002 | t0001 | g0050 | EAS | JPT | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| NA18950 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| NA18952 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| NA18959 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| NA18960 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| NA18964 | hp2 | a0002 | c0003 | t0001 | g0088 | EAS | JPT | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| NA18965 | hp1 | a0002 | c0002 | t0001 | g0055 | EAS | JPT | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| NA18974 | hp1 | a0002 | c0002 | t0001 | g0043 | EAS | JPT | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| NA18974 | hp2 | a0001 | c0004 | t0002 | g0068 | EAS | JPT | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| NA18982 | hp1 | a0001 | c0004 | t0002 | g0017 | EAS | JPT | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| NA18984 | hp1 | a0001 | c0004 | t0002 | g0066 | EAS | JPT | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| NA18986 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| NA19001 | hp2 | a0002 | c0002 | t0001 | g0051 | EAS | JPT | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| NA19003 | hp2 | a0002 | c0002 | t0001 | g0054 | EAS | JPT | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| NA19007 | hp1 | a0002 | c0002 | t0001 | g0048 | EAS | JPT | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| NA19009 | hp1 | a0001 | c0004 | t0002 | g0070 | EAS | JPT | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| NA19011 | hp2 | a0001 | c0004 | t0002 | g0062 | EAS | JPT | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| NA19030 | hp1 | a0003 | c0006 | t0001 | g0083 | AFR | LWK | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| NA19030 | hp2 | a0002 | c0003 | t0001 | g0034 | AFR | LWK | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| NA19043 | hp1 | a0001 | c0005 | t0001 | g0035 | AFR | LWK | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| NA19043 | hp2 | a0002 | c0003 | t0001 | g0034 | AFR | LWK | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| NA19059 | hp1 | a0002 | c0002 | t0001 | g0038 | EAS | JPT | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| NA19059 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| NA19065 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| NA19066 | hp1 | a0001 | c0004 | t0002 | g0017 | EAS | JPT | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| NA19066 | hp2 | a0002 | c0002 | t0001 | g0052 | EAS | JPT | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| NA19074 | hp2 | a0002 | c0002 | t0001 | g0049 | EAS | JPT | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| NA19076 | hp2 | a0002 | c0003 | t0001 | g0011 | EAS | JPT | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| NA19078 | hp1 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| NA19081 | hp2 | a0002 | c0003 | t0001 | g0011 | EAS | JPT | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| NA19087 | hp1 | a0002 | c0002 | t0001 | g0041 | EAS | JPT | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| NA19089 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| NA19091 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | YRI | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| NA19240 | hp2 | a0002 | c0002 | t0001 | g0015 | AFR | YRI | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| NA20129 | hp1 | a0002 | c0003 | t0001 | g0022 | AFR | ASW | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| NA20129 | hp2 | a0001 | c0004 | t0001 | g0059 | AFR | ASW | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| NA20805 | hp2 | a0002 | c0002 | t0001 | g0037 | EUR | TSI | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0184 | SAS | GIH | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| NA20905 | hp2 | a0002 | c0002 | t0001 | g0016 | SAS | GIH | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG02109 | hp1 | a0002 | c0002 | t0001 | g0014 | AFR | ACB | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG02109 | hp2 | a0001 | c0004 | t0002 | g0018 | AFR | ACB | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0195 | AFR | ACB | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0194 | AFR | ACB | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | ACB | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG03471 | hp1 | a0001 | c0004 | t0001 | g0074 | AFR | MSL | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG03471 | hp2 | a0002 | c0002 | t0001 | g0079 | AFR | MSL | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | USA | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | USA | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| NA18955 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| NA20300 | hp1 | a0001 | c0005 | t0001 | g0206 | AFR | USA | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | USA | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| NA21309 | hp1 | a0001 | c0004 | t0001 | g0021 | AFR | LWK | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| NA21309 | hp2 | a0001 | c0004 | t0001 | g0077 | AFR | LWK | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| homoSapiens | chm13v2 | a0005 | c0007 | t0001 | g0101 | REF | REF | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| homoSapiens | grch38p0 | a0002 | c0002 | t0001 | g0040 | REF | REF | HPF1_chr4_169724470_169762944 | HPF1 | chr4 | 169724470 | 169762944 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:169729580 | A | T | 1 | a0001 | 1 | HG01168.hp2 | stop_lost | HIGH | c.1039T>A | p.Ter347Argext*? | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 8/8 | 1106/1216 | 1039/1041 | 347/346 | chr4 | 169729580 | |||
| chr4:169742043 | T | C | 1 | a0003 | 2 | HG02886.hp2 NA19030.hp1 |
missense_variant | MODERATE | c.562A>G | p.Ile188Val | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 5/8 | 629/1216 | 562/1041 | 188/346 | chr4 | 169742043 | |||
| chr4:169742084 | C | T | 3 | a0001 a0003 a0004 |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(226): Show |
missense_variant | MODERATE | c.521G>A | p.Arg174Lys | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 5/8 | 588/1216 | 521/1041 | 174/346 | chr4 | 169742084 | |||
| chr4:169750081 | ATATTCCT others(2957): Show |
A | 1 | a0004 | 1 | HG03927.hp2 | exon_loss_variant&splice_acceptor_variant&splice_donor_variant&splice_region_variant&intron_variant | HIGH | c.208+631_398+454del | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 3/8 | chr4 | 169750081 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:169757842 | T | C | 4 | a0001c0001 a0002c0003 a0003c0006 others(1): Show |
225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
synonymous_variant | LOW | c.36A>G | p.Gly12Gly | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 1/8 | 103/1216 | 36/1041 | 12/346 | chr4 | 169757842 | |||
| chr4:169757848 | G | C | 2 | a0001c0005 a0002c0009 |
6 | HG02572.hp2 HG03540.hp1 HG03540.hp2 others(3): Show |
synonymous_variant | LOW | c.30C>G | p.Pro10Pro | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 1/8 | 97/1216 | 30/1041 | 10/346 | chr4 | 169757848 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:169729548 | AAT | A | 4 | a0001c0001t0002 a0001c0004t0002 a0002c0002t0002 others(1): Show |
22 | HG00099.hp1 HG01175.hp2 HG01358.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*28_*29delAT | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 8/8 | 28 | chr4 | 169729548 | ||||||
| chr4:169729571 | A | G | 1 | a0001c0001t0004 | 1 | HG03942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7T>C | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 8/8 | 7 | chr4 | 169729571 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:169729788 | A | G | 1 | a0001c0001t0001g0180 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.910-79T>C | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 7/7 | chr4 | 169729788 | |||||||
| chr4:169729938 | A | G | 1 | a0001c0004t0001g0020 | 2 | HG01109.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.910-229T>C | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 7/7 | chr4 | 169729938 | |||||||
| chr4:169730023 | C | T | 83 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(80): Show |
142 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.910-314G>A | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 7/7 | chr4 | 169730023 | |||||||
| chr4:169730126 | TCTCTCCC others(24): Show |
T | 1 | a0002c0002t0001g0038 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.910-448_910-418del others(31): Show |
HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 7/7 | chr4 | 169730126 | |||||||
| chr4:169730152 | G | A | 1 | a0001c0001t0001g0013 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.910-443C>T | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 7/7 | chr4 | 169730152 | |||||||
| chr4:169730255 | T | C | 2 | a0003c0006t0001g0083 a0003c0006t0001g0084 |
2 | HG02886.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.910-546A>G | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 7/7 | chr4 | 169730255 | |||||||
| chr4:169730261 | C | A | 1 | a0001c0001t0001g0191 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.910-552G>T | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 7/7 | chr4 | 169730261 | |||||||
| chr4:169730267 | C | A | 2 | a0001c0001t0002g0193 a0001c0001t0002g0194 |
2 | HG01891.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.910-558G>T | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 7/7 | chr4 | 169730267 | |||||||
| chr4:169730272 | G | A | 11 | a0001c0001t0002g0173 a0001c0004t0002g0017 a0001c0004t0002g0018 others(8): Show |
13 | HG00099.hp1 HG01981.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.910-563C>T | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 7/7 | chr4 | 169730272 | |||||||
| chr4:169730468 | T | C | 1 | a0001c0001t0002g0192 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.910-759A>G | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 7/7 | chr4 | 169730468 | |||||||
| chr4:169730646 | A | T | 191 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(188): Show |
297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.910-937T>A | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 7/7 | chr4 | 169730646 | |||||||
| chr4:169730660 | C | T | 87 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(84): Show |
146 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.910-951G>A | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 7/7 | chr4 | 169730660 | |||||||
| chr4:169730743 | A | T | 1 | a0001c0004t0001g0020 | 2 | HG01109.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.909+961T>A | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 7/7 | chr4 | 169730743 | |||||||
| chr4:169730804 | C | T | 1 | a0001c0001t0001g0120 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.909+900G>A | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 7/7 | chr4 | 169730804 | |||||||
| chr4:169730836 | G | T | 12 | a0001c0001t0002g0173 a0001c0001t0002g0192 a0001c0004t0002g0017 others(9): Show |
14 | HG00099.hp1 HG01358.hp2 HG01981.hp1 others(11): Show |
intron_variant | MODIFIER | c.909+868C>A | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 7/7 | chr4 | 169730836 | |||||||
| chr4:169731064 | A | G | 2 | a0001c0001t0001g0203 a0001c0001t0001g0204 |
2 | HG02723.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.909+640T>C | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 7/7 | chr4 | 169731064 | |||||||
| chr4:169731309 | C | T | 1 | a0001c0001t0001g0171 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.909+395G>A | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 7/7 | chr4 | 169731309 | |||||||
| chr4:169731384 | G | A | 1 | a0001c0001t0001g0152 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.909+320C>T | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 7/7 | chr4 | 169731384 | |||||||
| chr4:169731557 | T | A | 1 | a0001c0001t0001g0143 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.909+147A>T | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 7/7 | chr4 | 169731557 | |||||||
| chr4:169731618 | G | A | 2 | a0003c0006t0001g0083 a0003c0006t0001g0084 |
2 | HG02886.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.909+86C>T | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 7/7 | chr4 | 169731618 | |||||||
| chr4:169731649 | G | A | 1 | a0002c0002t0001g0044 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.909+55C>T | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 7/7 | chr4 | 169731649 | |||||||
| chr4:169732137 | A | AT | 16 | a0001c0001t0001g0167 a0001c0004t0001g0020 a0002c0002t0001g0009 others(13): Show |
21 | HG00140.hp1 HG00280.hp2 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.737-262dupA | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 6/7 | chr4 | 169732137 | |||||||
| chr4:169732137 | AT | A | 121 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(118): Show |
190 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.737-262delA | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 6/7 | chr4 | 169732137 | |||||||
| chr4:169732137 | ATT | A | 11 | a0001c0001t0001g0142 a0001c0001t0002g0173 a0001c0004t0002g0017 others(8): Show |
13 | HG00099.hp1 HG02109.hp2 HG02132.hp2 others(10): Show |
intron_variant | MODIFIER | c.737-263_737-262del others(2): Show |
HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 6/7 | chr4 | 169732137 | |||||||
| chr4:169732143 | T | C | 2 | a0001c0001t0001g0188 a0001c0001t0001g0190 |
2 | HG02896.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.737-267A>G | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 6/7 | chr4 | 169732143 | |||||||
| chr4:169732346 | G | A | 15 | a0001c0001t0001g0007 a0001c0001t0001g0103 a0001c0001t0001g0107 others(12): Show |
20 | HG00544.hp1 HG01070.hp1 HG01099.hp2 others(17): Show |
intron_variant | MODIFIER | c.737-470C>T | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 6/7 | chr4 | 169732346 | |||||||
| chr4:169732463 | C | G | 1 | a0001c0004t0001g0020 | 2 | HG01109.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.737-587G>C | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 6/7 | chr4 | 169732463 | |||||||
| chr4:169732472 | G | A | 1 | a0001c0004t0001g0020 | 2 | HG01109.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.737-596C>T | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 6/7 | chr4 | 169732472 | |||||||
| chr4:169732492 | A | G | 88 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(85): Show |
147 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.737-616T>C | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 6/7 | chr4 | 169732492 | |||||||
| chr4:169732503 | A | C | 1 | a0001c0001t0001g0189 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.737-627T>G | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 6/7 | chr4 | 169732503 | |||||||
| chr4:169732743 | C | G | 2 | a0001c0001t0001g0189 a0001c0004t0001g0020 |
3 | HG01109.hp1 HG02976.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.737-867G>C | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 6/7 | chr4 | 169732743 | |||||||
| chr4:169732758 | C | T | 4 | a0001c0001t0002g0099 a0001c0001t0002g0155 a0002c0003t0002g0201 others(1): Show |
4 | HG01175.hp2 HG01891.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.737-882G>A | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 6/7 | chr4 | 169732758 | |||||||
| chr4:169732762 | T | G | 1 | a0001c0005t0001g0207 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.737-886A>C | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 6/7 | chr4 | 169732762 | |||||||
| chr4:169732769 | A | G | 12 | a0001c0001t0002g0173 a0001c0001t0002g0192 a0001c0004t0002g0017 others(9): Show |
14 | HG00099.hp1 HG01358.hp2 HG01981.hp1 others(11): Show |
intron_variant | MODIFIER | c.737-893T>C | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 6/7 | chr4 | 169732769 | |||||||
| chr4:169733497 | A | G | 28 | a0001c0001t0001g0082 a0001c0001t0001g0095 a0001c0001t0001g0100 others(25): Show |
33 | HG00099.hp1 HG01884.hp1 HG02109.hp2 others(30): Show |
intron_variant | MODIFIER | c.737-1621T>C | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 6/7 | chr4 | 169733497 | |||||||
| chr4:169733533 | T | A | 1 | a0001c0001t0001g0186 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.737-1657A>T | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 6/7 | chr4 | 169733533 | |||||||
| chr4:169733691 | T | C | 12 | a0001c0001t0001g0189 a0001c0001t0001g0191 a0001c0001t0001g0198 others(9): Show |
13 | HG01109.hp1 HG01175.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.737-1815A>G | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 6/7 | chr4 | 169733691 | |||||||
| chr4:169733825 | G | A | 2 | a0001c0001t0001g0100 a0001c0001t0002g0099 |
2 | HG02647.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.737-1949C>T | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 6/7 | chr4 | 169733825 | |||||||
| chr4:169733842 | C | T | 3 | a0001c0001t0001g0203 a0001c0001t0001g0204 a0002c0002t0001g0015 |
4 | HG02723.hp2 HG03041.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.737-1966G>A | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 6/7 | chr4 | 169733842 | |||||||
| chr4:169733894 | C | CA | 19 | a0001c0001t0001g0004 a0001c0001t0001g0082 a0001c0001t0001g0100 others(16): Show |
27 | HG00639.hp1 HG01884.hp1 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.737-2019dupT | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 6/7 | chr4 | 169733894 | |||||||
| chr4:169733894 | CA | C | 102 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(99): Show |
168 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.737-2019delT | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 6/7 | chr4 | 169733894 | |||||||
| chr4:169733910 | A | C | 6 | a0001c0004t0001g0019 a0001c0004t0001g0021 a0001c0004t0001g0073 others(3): Show |
8 | HG02572.hp1 HG02615.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.737-2034T>G | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 6/7 | chr4 | 169733910 | |||||||
| chr4:169733953 | C | T | 2 | a0001c0001t0001g0140 a0001c0001t0001g0141 |
2 | NA18955.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.737-2077G>A | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 6/7 | chr4 | 169733953 | |||||||
| chr4:169734008 | T | C | 1 | a0001c0004t0002g0065 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.737-2132A>G | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 6/7 | chr4 | 169734008 | |||||||
| chr4:169734142 | G | A | 1 | a0001c0001t0001g0147 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.737-2266C>T | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 6/7 | chr4 | 169734142 | |||||||
| chr4:169734277 | G | A | 1 | a0001c0001t0001g0185 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.737-2401C>T | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 6/7 | chr4 | 169734277 | |||||||
| chr4:169734292 | T | A | 3 | a0001c0001t0001g0189 a0001c0001t0001g0191 a0001c0004t0001g0020 |
4 | HG01109.hp1 HG02976.hp2 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.737-2416A>T | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 6/7 | chr4 | 169734292 | |||||||
| chr4:169734299 | G | A | 1 | a0001c0001t0001g0114 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.737-2423C>T | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 6/7 | chr4 | 169734299 | |||||||
| chr4:169734469 | C | A | 1 | a0002c0002t0001g0045 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.737-2593G>T | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 6/7 | chr4 | 169734469 | |||||||
| chr4:169734737 | A | G | 3 | a0001c0001t0001g0119 a0001c0001t0001g0166 a0001c0001t0001g0170 |
3 | HG00642.hp2 HG01167.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.737-2861T>C | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 6/7 | chr4 | 169734737 | |||||||
| chr4:169735127 | C | CA | 45 | a0001c0001t0001g0004 a0001c0001t0001g0032 a0001c0001t0001g0082 others(42): Show |
58 | HG00099.hp1 HG00639.hp1 HG01070.hp2 others(55): Show |
intron_variant | MODIFIER | c.736+2532dupT | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 6/7 | chr4 | 169735127 | |||||||
| chr4:169735127 | CA | C | 6 | a0001c0001t0001g0105 a0001c0001t0001g0140 a0001c0001t0001g0153 others(3): Show |
7 | HG01168.hp1 HG02809.hp2 NA18955.hp1 others(4): Show |
intron_variant | MODIFIER | c.736+2532delT | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 6/7 | chr4 | 169735127 | |||||||
| chr4:169735140 | A | G | 1 | a0001c0004t0001g0020 | 2 | HG01109.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.736+2520T>C | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 6/7 | chr4 | 169735140 | |||||||
| chr4:169735142 | A | G | 2 | a0001c0001t0001g0026 a0001c0001t0001g0113 |
3 | HG00140.hp2 HG01261.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.736+2518T>C | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 6/7 | chr4 | 169735142 | |||||||
| chr4:169735466 | G | A | 3 | a0002c0003t0001g0023 a0002c0003t0001g0024 a0002c0003t0001g0091 |
5 | HG01109.hp2 HG02258.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.736+2194C>T | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 6/7 | chr4 | 169735466 | |||||||
| chr4:169735526 | A | C | 3 | a0001c0001t0001g0189 a0001c0001t0001g0191 a0001c0004t0001g0020 |
4 | HG01109.hp1 HG02976.hp2 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.736+2134T>G | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 6/7 | chr4 | 169735526 | |||||||
| chr4:169735932 | T | TA | 30 | a0001c0001t0001g0082 a0001c0001t0001g0100 a0001c0001t0001g0136 others(27): Show |
37 | HG01109.hp1 HG01243.hp2 HG01884.hp1 others(34): Show |
intron_variant | MODIFIER | c.736+1727dupT | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 6/7 | chr4 | 169735932 | |||||||
| chr4:169735932 | T | TAA | 13 | a0001c0001t0001g0004 a0001c0001t0001g0095 a0001c0001t0001g0197 others(10): Show |
21 | HG00639.hp1 HG01884.hp2 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.736+1726_736+1727d others(4): Show |
HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 6/7 | chr4 | 169735932 | |||||||
| chr4:169735932 | TA | T | 23 | a0001c0001t0001g0090 a0001c0001t0002g0173 a0001c0004t0002g0017 others(20): Show |
28 | HG00099.hp1 HG01981.hp1 HG02109.hp2 others(25): Show |
intron_variant | MODIFIER | c.736+1727delT | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 6/7 | chr4 | 169735932 | |||||||
| chr4:169735947 | A | AC | 3 | a0001c0001t0002g0192 a0001c0001t0002g0193 a0001c0001t0002g0194 |
3 | HG01358.hp2 HG01891.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.736+1712_736+1713i others(3): Show |
HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 6/7 | chr4 | 169735947 | |||||||
| chr4:169736107 | G | A | 191 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(188): Show |
297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.736+1553C>T | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 6/7 | chr4 | 169736107 | |||||||
| chr4:169736176 | C | T | 2 | a0001c0001t0001g0004 a0001c0001t0001g0197 |
8 | HG00639.hp1 HG01884.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.736+1484G>A | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 6/7 | chr4 | 169736176 | |||||||
| chr4:169736190 | G | A | 37 | a0001c0001t0001g0190 a0001c0001t0001g0203 a0001c0001t0001g0204 others(34): Show |
65 | HG00140.hp1 HG00280.hp2 HG00558.hp2 others(62): Show |
intron_variant | MODIFIER | c.736+1470C>T | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 6/7 | chr4 | 169736190 | |||||||
| chr4:169736216 | A | G | 13 | a0001c0001t0001g0090 a0001c0001t0001g0188 a0001c0001t0002g0173 others(10): Show |
15 | HG00099.hp1 HG01981.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.736+1444T>C | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 6/7 | chr4 | 169736216 | |||||||
| chr4:169736359 | C | CA | 99 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(96): Show |
158 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.736+1300dupT | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 6/7 | chr4 | 169736359 | |||||||
| chr4:169736359 | C | CAA | 13 | a0001c0001t0001g0008 a0001c0001t0001g0031 a0001c0001t0001g0081 others(10): Show |
17 | HG01175.hp1 HG01175.hp2 HG01358.hp1 others(14): Show |
intron_variant | MODIFIER | c.736+1299_736+1300d others(4): Show |
HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 6/7 | chr4 | 169736359 | |||||||
| chr4:169736375 | AAG | A | 16 | a0001c0001t0001g0082 a0001c0001t0001g0095 a0001c0001t0001g0100 others(13): Show |
19 | HG01884.hp1 HG02280.hp2 HG02486.hp1 others(16): Show |
intron_variant | MODIFIER | c.736+1283_736+1284d others(4): Show |
HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 6/7 | chr4 | 169736375 | |||||||
| chr4:169736376 | AG | A | 8 | a0001c0001t0001g0004 a0001c0001t0001g0189 a0001c0001t0001g0190 others(5): Show |
12 | HG00639.hp1 HG01884.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.736+1283delC | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 6/7 | chr4 | 169736376 | |||||||
| chr4:169736377 | G | A | 156 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(153): Show |
251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.736+1283C>T | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 6/7 | chr4 | 169736377 | |||||||
| chr4:169736509 | C | CA | 13 | a0001c0001t0001g0090 a0001c0001t0001g0188 a0001c0001t0002g0173 others(10): Show |
15 | HG00099.hp1 HG01981.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.736+1150dupT | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 6/7 | chr4 | 169736509 | |||||||
| chr4:169736515 | C | A | 13 | a0001c0001t0001g0090 a0001c0001t0001g0188 a0001c0001t0002g0173 others(10): Show |
15 | HG00099.hp1 HG01981.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.736+1145G>T | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 6/7 | chr4 | 169736515 | |||||||
| chr4:169736678 | C | T | 1 | a0002c0002t0002g0057 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.736+982G>A | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 6/7 | chr4 | 169736678 | |||||||
| chr4:169736692 | G | C | 1 | a0001c0001t0001g0150 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.736+968C>G | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 6/7 | chr4 | 169736692 | |||||||
| chr4:169736700 | C | T | 1 | a0001c0001t0001g0190 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.736+960G>A | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 6/7 | chr4 | 169736700 | |||||||
| chr4:169736725 | T | C | 1 | a0001c0001t0002g0155 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.736+935A>G | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 6/7 | chr4 | 169736725 | |||||||
| chr4:169736772 | C | A | 1 | a0001c0001t0001g0128 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.736+888G>T | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 6/7 | chr4 | 169736772 | |||||||
| chr4:169736847 | T | C | 73 | a0001c0001t0001g0004 a0001c0001t0001g0082 a0001c0001t0001g0095 others(70): Show |
113 | HG00140.hp1 HG00280.hp2 HG00558.hp2 others(110): Show |
intron_variant | MODIFIER | c.736+813A>G | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 6/7 | chr4 | 169736847 | |||||||
| chr4:169736877 | C | T | 35 | a0001c0001t0001g0004 a0001c0001t0001g0082 a0001c0001t0001g0090 others(32): Show |
46 | HG00099.hp1 HG00639.hp1 HG01884.hp1 others(43): Show |
intron_variant | MODIFIER | c.736+783G>A | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 6/7 | chr4 | 169736877 | |||||||
| chr4:169736879 | T | C | 35 | a0001c0001t0001g0004 a0001c0001t0001g0082 a0001c0001t0001g0090 others(32): Show |
46 | HG00099.hp1 HG00639.hp1 HG01884.hp1 others(43): Show |
intron_variant | MODIFIER | c.736+781A>G | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 6/7 | chr4 | 169736879 | |||||||
| chr4:169736898 | C | T | 167 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(164): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.736+762G>A | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 6/7 | chr4 | 169736898 | |||||||
| chr4:169736941 | G | A | 29 | a0002c0002t0001g0002 a0002c0002t0001g0009 a0002c0002t0001g0014 others(26): Show |
57 | HG00140.hp1 HG00280.hp2 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.736+719C>T | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 6/7 | chr4 | 169736941 | |||||||
| chr4:169737082 | C | T | 1 | a0001c0001t0001g0190 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.736+578G>A | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 6/7 | chr4 | 169737082 | |||||||
| chr4:169737128 | G | A | 200 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(197): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.736+532C>T | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 6/7 | chr4 | 169737128 | |||||||
| chr4:169737181 | T | A | 29 | a0002c0002t0001g0002 a0002c0002t0001g0009 a0002c0002t0001g0014 others(26): Show |
57 | HG00140.hp1 HG00280.hp2 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.736+479A>T | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 6/7 | chr4 | 169737181 | |||||||
| chr4:169737269 | G | T | 146 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(143): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.736+391C>A | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 6/7 | chr4 | 169737269 | |||||||
| chr4:169737289 | C | CA | 101 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(98): Show |
168 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.736+370dupT | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 6/7 | chr4 | 169737289 | |||||||
| chr4:169737289 | C | CAA | 11 | a0001c0001t0001g0114 a0001c0001t0001g0151 a0001c0001t0001g0152 others(8): Show |
12 | HG01109.hp1 HG01175.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.736+369_736+370dup others(2): Show |
HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 6/7 | chr4 | 169737289 | |||||||
| chr4:169737289 | CA | C | 21 | a0001c0001t0001g0090 a0001c0001t0001g0188 a0001c0001t0001g0189 others(18): Show |
23 | HG01891.hp2 HG01981.hp1 HG02109.hp2 others(20): Show |
intron_variant | MODIFIER | c.736+370delT | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 6/7 | chr4 | 169737289 | |||||||
| chr4:169737296 | A | C | 7 | a0001c0001t0001g0095 a0001c0001t0001g0156 a0001c0001t0001g0195 others(4): Show |
8 | HG02280.hp2 HG02486.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.736+364T>G | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 6/7 | chr4 | 169737296 | |||||||
| chr4:169737300 | A | AC | 6 | a0001c0001t0001g0104 a0001c0001t0001g0158 a0001c0001t0001g0159 others(3): Show |
6 | HG01346.hp2 HG01433.hp1 HG01978.hp2 others(3): Show |
intron_variant | MODIFIER | c.736+359_736+360ins others(1): Show |
HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 6/7 | chr4 | 169737300 | |||||||
| chr4:169737300 | A | C | 9 | a0001c0001t0001g0082 a0001c0001t0001g0100 a0001c0001t0002g0099 others(6): Show |
11 | HG01884.hp1 HG02615.hp1 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.736+360T>G | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 6/7 | chr4 | 169737300 | |||||||
| chr4:169737303 | A | C | 2 | a0001c0001t0001g0004 a0001c0001t0001g0197 |
8 | HG00639.hp1 HG01884.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.736+357T>G | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 6/7 | chr4 | 169737303 | |||||||
| chr4:169737304 | A | C | 20 | a0001c0001t0001g0190 a0001c0004t0002g0017 a0001c0004t0002g0018 others(17): Show |
25 | HG01981.hp1 HG02109.hp2 HG02132.hp2 others(22): Show |
intron_variant | MODIFIER | c.736+356T>G | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 6/7 | chr4 | 169737304 | |||||||
| chr4:169737307 | AC | A | 22 | a0001c0001t0001g0004 a0001c0001t0001g0082 a0001c0001t0001g0095 others(19): Show |
31 | HG00639.hp1 HG01884.hp1 HG01884.hp2 others(28): Show |
intron_variant | MODIFIER | c.736+352delG | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 6/7 | chr4 | 169737307 | |||||||
| chr4:169737410 | G | T | 2 | a0002c0003t0001g0022 a0002c0003t0001g0089 |
3 | HG02055.hp2 HG03098.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.736+250C>A | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 6/7 | chr4 | 169737410 | |||||||
| chr4:169737490 | C | T | 3 | a0001c0001t0002g0192 a0001c0001t0002g0193 a0001c0001t0002g0194 |
3 | HG01358.hp2 HG01891.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.736+170G>A | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 6/7 | chr4 | 169737490 | |||||||
| chr4:169737580 | A | G | 51 | a0001c0001t0001g0090 a0001c0001t0001g0188 a0001c0004t0002g0017 others(48): Show |
82 | HG00140.hp1 HG00280.hp2 HG00558.hp2 others(79): Show |
intron_variant | MODIFIER | c.736+80T>C | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 6/7 | chr4 | 169737580 | |||||||
| chr4:169737616 | T | C | 2 | a0001c0004t0001g0010 a0001c0004t0001g0072 |
4 | HG01884.hp1 HG02886.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.736+44A>G | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 6/7 | chr4 | 169737616 | |||||||
| chr4:169737793 | C | CA | 45 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(42): Show |
77 | HG00140.hp1 HG00280.hp2 HG00558.hp2 others(74): Show |
intron_variant | MODIFIER | c.649-47dupT | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 5/7 | chr4 | 169737793 | |||||||
| chr4:169737798 | A | AAG | 22 | a0001c0001t0001g0004 a0001c0001t0001g0082 a0001c0001t0001g0095 others(19): Show |
31 | HG00639.hp1 HG01884.hp1 HG01884.hp2 others(28): Show |
intron_variant | MODIFIER | c.649-52_649-51insCT | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 5/7 | chr4 | 169737798 | |||||||
| chr4:169737863 | A | G | 1 | a0001c0001t0001g0183 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.649-116T>C | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 5/7 | chr4 | 169737863 | |||||||
| chr4:169737913 | T | TGAAAATC others(278): Show |
12 | a0001c0001t0001g0090 a0001c0001t0001g0188 a0001c0004t0002g0017 others(9): Show |
14 | HG01981.hp1 HG02109.hp2 HG02132.hp2 others(11): Show |
intron_variant | MODIFIER | c.649-167_649-166ins others(285): Show |
HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 5/7 | chr4 | 169737913 | |||||||
| chr4:169738407 | G | C | 3 | a0001c0004t0002g0062 a0001c0004t0002g0065 a0001c0004t0002g0070 |
3 | HG01981.hp1 NA19009.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.649-660C>G | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 5/7 | chr4 | 169738407 | |||||||
| chr4:169738459 | C | G | 98 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(95): Show |
161 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.649-712G>C | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 5/7 | chr4 | 169738459 | |||||||
| chr4:169738465 | T | C | 1 | a0001c0001t0001g0157 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.649-718A>G | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 5/7 | chr4 | 169738465 | |||||||
| chr4:169738469 | C | T | 5 | a0001c0001t0002g0192 a0001c0001t0002g0193 a0001c0001t0002g0194 others(2): Show |
5 | HG01358.hp2 HG01891.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.649-722G>A | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 5/7 | chr4 | 169738469 | |||||||
| chr4:169738791 | A | G | 2 | a0001c0004t0001g0010 a0001c0004t0001g0072 |
4 | HG01884.hp1 HG02886.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.649-1044T>C | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 5/7 | chr4 | 169738791 | |||||||
| chr4:169738795 | A | C | 5 | a0002c0002t0002g0057 a0002c0003t0001g0086 a0002c0003t0002g0085 others(2): Show |
5 | HG01891.hp2 HG02723.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.649-1048T>G | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 5/7 | chr4 | 169738795 | |||||||
| chr4:169738839 | G | A | 3 | a0001c0001t0001g0203 a0001c0001t0001g0204 a0001c0001t0001g0205 |
3 | HG02280.hp1 HG02723.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.649-1092C>T | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 5/7 | chr4 | 169738839 | |||||||
| chr4:169738841 | G | A | 5 | a0001c0001t0001g0104 a0001c0001t0001g0158 a0001c0001t0001g0159 others(2): Show |
5 | HG01346.hp2 HG01433.hp1 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.649-1094C>T | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 5/7 | chr4 | 169738841 | |||||||
| chr4:169738865 | C | A | 1 | a0001c0001t0002g0192 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.649-1118G>T | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 5/7 | chr4 | 169738865 | |||||||
| chr4:169738891 | A | G | 1 | a0001c0004t0002g0065 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.649-1144T>C | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 5/7 | chr4 | 169738891 | |||||||
| chr4:169738935 | A | G | 3 | a0002c0003t0001g0022 a0002c0003t0001g0086 a0002c0003t0001g0089 |
4 | HG02055.hp2 HG03098.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.649-1188T>C | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 5/7 | chr4 | 169738935 | |||||||
| chr4:169738987 | G | C | 3 | a0002c0002t0001g0078 a0002c0002t0001g0079 a0002c0009t0001g0209 |
3 | HG02258.hp1 HG03471.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.649-1240C>G | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 5/7 | chr4 | 169738987 | |||||||
| chr4:169738995 | G | C | 1 | a0001c0001t0001g0032 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.649-1248C>G | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 5/7 | chr4 | 169738995 | |||||||
| chr4:169739171 | G | A | 1 | a0001c0001t0001g0160 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.649-1424C>T | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 5/7 | chr4 | 169739171 | |||||||
| chr4:169739177 | T | C | 1 | a0002c0002t0001g0049 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.649-1430A>G | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 5/7 | chr4 | 169739177 | |||||||
| chr4:169739394 | C | G | 2 | a0001c0001t0001g0029 a0001c0001t0001g0136 |
3 | NA18947.hp2 NA18989.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.649-1647G>C | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 5/7 | chr4 | 169739394 | |||||||
| chr4:169739454 | A | C | 10 | a0001c0004t0002g0017 a0001c0004t0002g0018 a0001c0004t0002g0062 others(7): Show |
12 | HG01981.hp1 HG02109.hp2 HG02132.hp2 others(9): Show |
intron_variant | MODIFIER | c.649-1707T>G | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 5/7 | chr4 | 169739454 | |||||||
| chr4:169739467 | G | A | 1 | a0002c0003t0001g0093 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.649-1720C>T | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 5/7 | chr4 | 169739467 | |||||||
| chr4:169739768 | C | T | 3 | a0002c0002t0001g0078 a0002c0002t0001g0079 a0002c0009t0001g0209 |
3 | HG02258.hp1 HG03471.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.649-2021G>A | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 5/7 | chr4 | 169739768 | |||||||
| chr4:169739770 | G | A | 2 | a0002c0002t0001g0050 a0002c0002t0001g0051 |
2 | NA18950.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.649-2023C>T | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 5/7 | chr4 | 169739770 | |||||||
| chr4:169739829 | C | T | 9 | a0001c0001t0001g0189 a0001c0001t0001g0191 a0001c0004t0001g0019 others(6): Show |
11 | HG02572.hp1 HG02615.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.649-2082G>A | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 5/7 | chr4 | 169739829 | |||||||
| chr4:169739953 | G | T | 1 | a0002c0003t0001g0022 | 2 | HG03098.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.648+2004C>A | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 5/7 | chr4 | 169739953 | |||||||
| chr4:169740012 | T | G | 29 | a0002c0002t0001g0002 a0002c0002t0001g0009 a0002c0002t0001g0014 others(26): Show |
57 | HG00140.hp1 HG00280.hp2 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.648+1945A>C | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 5/7 | chr4 | 169740012 | |||||||
| chr4:169740080 | T | C | 1 | a0001c0004t0001g0020 | 2 | HG01109.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.648+1877A>G | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 5/7 | chr4 | 169740080 | |||||||
| chr4:169740324 | G | T | 2 | a0002c0003t0001g0022 a0002c0003t0001g0089 |
3 | HG02055.hp2 HG03098.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.648+1633C>A | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 5/7 | chr4 | 169740324 | |||||||
| chr4:169740511 | C | T | 1 | a0002c0002t0001g0037 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.648+1446G>A | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 5/7 | chr4 | 169740511 | |||||||
| chr4:169740599 | T | A | 39 | a0002c0002t0001g0002 a0002c0002t0001g0009 a0002c0002t0001g0014 others(36): Show |
68 | HG00140.hp1 HG00280.hp2 HG00558.hp2 others(65): Show |
intron_variant | MODIFIER | c.648+1358A>T | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 5/7 | chr4 | 169740599 | |||||||
| chr4:169740670 | T | C | 1 | a0001c0001t0001g0161 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.648+1287A>G | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 5/7 | chr4 | 169740670 | |||||||
| chr4:169740829 | T | C | 1 | a0001c0004t0001g0061 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.648+1128A>G | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 5/7 | chr4 | 169740829 | |||||||
| chr4:169740998 | C | T | 2 | a0001c0001t0001g0100 a0001c0001t0002g0099 |
2 | HG02647.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.648+959G>A | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 5/7 | chr4 | 169740998 | |||||||
| chr4:169741110 | C | G | 1 | a0001c0001t0001g0190 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.648+847G>C | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 5/7 | chr4 | 169741110 | |||||||
| chr4:169741124 | C | T | 37 | a0002c0002t0001g0002 a0002c0002t0001g0009 a0002c0002t0001g0014 others(34): Show |
65 | HG00140.hp1 HG00280.hp2 HG00558.hp2 others(62): Show |
intron_variant | MODIFIER | c.648+833G>A | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 5/7 | chr4 | 169741124 | |||||||
| chr4:169741150 | A | C | 10 | a0001c0001t0001g0082 a0001c0001t0001g0100 a0001c0001t0002g0099 others(7): Show |
12 | HG01884.hp1 HG02602.hp2 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.648+807T>G | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 5/7 | chr4 | 169741150 | |||||||
| chr4:169741151 | G | C | 1 | a0001c0001t0001g0128 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.648+806C>G | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 5/7 | chr4 | 169741151 | |||||||
| chr4:169741211 | A | C | 1 | a0001c0001t0001g0189 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.648+746T>G | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 5/7 | chr4 | 169741211 | |||||||
| chr4:169741338 | T | G | 11 | a0002c0003t0001g0011 a0002c0003t0001g0022 a0002c0003t0001g0025 others(8): Show |
15 | HG02055.hp2 HG02735.hp2 HG02896.hp2 others(12): Show |
intron_variant | MODIFIER | c.648+619A>C | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 5/7 | chr4 | 169741338 | |||||||
| chr4:169741357 | C | G | 2 | a0001c0001t0002g0193 a0001c0001t0002g0194 |
2 | HG01891.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.648+600G>C | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 5/7 | chr4 | 169741357 | |||||||
| chr4:169741360 | C | T | 2 | a0002c0003t0001g0034 a0002c0003t0001g0196 |
3 | HG02809.hp2 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.648+597G>A | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 5/7 | chr4 | 169741360 | |||||||
| chr4:169741476 | T | C | 191 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(188): Show |
297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.648+481A>G | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 5/7 | chr4 | 169741476 | |||||||
| chr4:169741691 | G | C | 13 | a0001c0001t0001g0189 a0001c0001t0001g0191 a0001c0001t0001g0203 others(10): Show |
16 | HG01109.hp1 HG02280.hp1 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.648+266C>G | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 5/7 | chr4 | 169741691 | |||||||
| chr4:169741753 | T | C | 3 | a0002c0003t0001g0011 a0002c0003t0001g0088 a0002c0003t0001g0094 |
5 | HG04184.hp1 NA18939.hp2 NA18964.hp2 others(2): Show |
intron_variant | MODIFIER | c.648+204A>G | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 5/7 | chr4 | 169741753 | |||||||
| chr4:169741815 | A | G | 4 | a0001c0001t0001g0003 a0001c0001t0001g0116 a0001c0001t0001g0118 others(1): Show |
11 | HG00597.hp2 HG00609.hp2 HG02027.hp2 others(8): Show |
intron_variant | MODIFIER | c.648+142T>C | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 5/7 | chr4 | 169741815 | |||||||
| chr4:169742170 | C | G | 191 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(188): Show |
297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.498-63G>C | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 4/7 | chr4 | 169742170 | |||||||
| chr4:169742341 | C | T | 2 | a0002c0003t0001g0086 a0002c0003t0002g0085 |
2 | HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.498-234G>A | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 4/7 | chr4 | 169742341 | |||||||
| chr4:169742391 | T | C | 2 | a0001c0001t0001g0104 a0001c0001t0001g0165 |
2 | HG01346.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.498-284A>G | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 4/7 | chr4 | 169742391 | |||||||
| chr4:169742420 | A | G | 1 | a0001c0001t0001g0134 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.498-313T>C | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 4/7 | chr4 | 169742420 | |||||||
| chr4:169742531 | G | A | 1 | a0001c0001t0001g0115 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.498-424C>T | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 4/7 | chr4 | 169742531 | |||||||
| chr4:169742561 | G | A | 9 | a0001c0001t0001g0189 a0001c0001t0001g0191 a0001c0004t0001g0019 others(6): Show |
11 | HG02572.hp1 HG02615.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.498-454C>T | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 4/7 | chr4 | 169742561 | |||||||
| chr4:169742589 | A | G | 36 | a0001c0001t0001g0028 a0001c0001t0001g0133 a0001c0001t0001g0169 others(33): Show |
62 | HG00140.hp1 HG00280.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.498-482T>C | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 4/7 | chr4 | 169742589 | |||||||
| chr4:169742597 | C | T | 6 | a0001c0004t0002g0017 a0001c0004t0002g0062 a0001c0004t0002g0065 others(3): Show |
7 | HG01981.hp1 HG02132.hp2 NA18982.hp1 others(4): Show |
intron_variant | MODIFIER | c.498-490G>A | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 4/7 | chr4 | 169742597 | |||||||
| chr4:169742598 | C | G | 2 | a0001c0001t0001g0132 a0001c0001t0001g0178 |
2 | HG00280.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.498-491G>C | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 4/7 | chr4 | 169742598 | |||||||
| chr4:169742603 | T | C | 1 | a0001c0001t0001g0127 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.498-496A>G | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 4/7 | chr4 | 169742603 | |||||||
| chr4:169742608 | A | C | 124 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(121): Show |
196 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(193): Show |
intron_variant | MODIFIER | c.498-501T>G | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 4/7 | chr4 | 169742608 | |||||||
| chr4:169742608 | A | T | 61 | a0001c0001t0001g0082 a0001c0001t0001g0100 a0001c0001t0001g0188 others(58): Show |
93 | HG00140.hp1 HG00280.hp2 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.498-501T>A | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 4/7 | chr4 | 169742608 | |||||||
| chr4:169742617 | C | T | 1 | a0001c0001t0004g0168 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.498-510G>A | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 4/7 | chr4 | 169742617 | |||||||
| chr4:169742618 | C | T | 170 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(167): Show |
272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.498-511G>A | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 4/7 | chr4 | 169742618 | |||||||
| chr4:169742634 | T | C | 1 | a0001c0001t0001g0167 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.498-527A>G | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 4/7 | chr4 | 169742634 | |||||||
| chr4:169742642 | A | G | 1 | a0002c0002t0001g0042 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.498-535T>C | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 4/7 | chr4 | 169742642 | |||||||
| chr4:169742656 | A | G | 2 | a0001c0001t0001g0130 a0002c0002t0001g0042 |
2 | HG02040.hp1 NA18942.hp2 |
intron_variant | MODIFIER | c.498-549T>C | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 4/7 | chr4 | 169742656 | |||||||
| chr4:169742738 | A | G | 1 | a0001c0001t0001g0129 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.498-631T>C | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 4/7 | chr4 | 169742738 | |||||||
| chr4:169742754 | T | G | 1 | a0001c0004t0001g0020 | 2 | HG01109.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.498-647A>C | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 4/7 | chr4 | 169742754 | |||||||
| chr4:169742901 | G | A | 1 | a0001c0001t0001g0105 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.498-794C>T | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 4/7 | chr4 | 169742901 | |||||||
| chr4:169742975 | C | T | 1 | a0001c0001t0001g0128 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.498-868G>A | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 4/7 | chr4 | 169742975 | |||||||
| chr4:169743008 | C | T | 1 | a0002c0003t0001g0089 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.498-901G>A | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 4/7 | chr4 | 169743008 | |||||||
| chr4:169743047 | T | C | 3 | a0001c0001t0001g0203 a0001c0001t0001g0204 a0001c0001t0001g0205 |
3 | HG02280.hp1 HG02723.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.498-940A>G | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 4/7 | chr4 | 169743047 | |||||||
| chr4:169743094 | C | CA | 36 | a0001c0001t0001g0082 a0001c0001t0001g0100 a0001c0001t0001g0189 others(33): Show |
65 | HG00280.hp2 HG00558.hp2 HG00621.hp2 others(62): Show |
intron_variant | MODIFIER | c.498-988dupT | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 4/7 | chr4 | 169743094 | |||||||
| chr4:169743106 | C | A | 3 | a0001c0001t0004g0168 a0002c0002t0001g0016 a0002c0002t0001g0053 |
4 | HG03491.hp1 HG03492.hp2 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.498-999G>T | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 4/7 | chr4 | 169743106 | |||||||
| chr4:169743111 | A | G | 1 | a0001c0001t0001g0191 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.498-1004T>C | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 4/7 | chr4 | 169743111 | |||||||
| chr4:169743134 | T | C | 1 | a0001c0001t0001g0126 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.498-1027A>G | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 4/7 | chr4 | 169743134 | |||||||
| chr4:169743408 | CCTTTT | C | 3 | a0001c0001t0001g0203 a0001c0001t0001g0204 a0001c0001t0001g0205 |
3 | HG02280.hp1 HG02723.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.498-1306_498-1302d others(7): Show |
HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 4/7 | chr4 | 169743408 | |||||||
| chr4:169743408 | CCTTTTTT | C | 5 | a0001c0004t0001g0019 a0001c0004t0001g0021 a0001c0004t0001g0074 others(2): Show |
7 | HG02615.hp2 HG02818.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.498-1308_498-1302d others(9): Show |
HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 4/7 | chr4 | 169743408 | |||||||
| chr4:169743409 | C | CT | 13 | a0001c0001t0001g0026 a0001c0001t0001g0100 a0001c0001t0001g0113 others(10): Show |
13 | HG00140.hp2 HG01261.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.498-1303dupA | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 4/7 | chr4 | 169743409 | |||||||
| chr4:169743409 | C | CTTTTT | 5 | a0001c0001t0001g0004 a0001c0001t0001g0197 a0001c0001t0001g0198 others(2): Show |
7 | HG00639.hp1 HG01891.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.498-1307_498-1303d others(7): Show |
HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 4/7 | chr4 | 169743409 | |||||||
| chr4:169743409 | CT | C | 105 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(102): Show |
150 | HG00140.hp1 HG00280.hp1 HG00544.hp2 others(147): Show |
intron_variant | MODIFIER | c.498-1303delA | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 4/7 | chr4 | 169743409 | |||||||
| chr4:169743409 | CTT | C | 38 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0090 others(35): Show |
65 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(62): Show |
intron_variant | MODIFIER | c.498-1304_498-1303d others(4): Show |
HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 4/7 | chr4 | 169743409 | |||||||
| chr4:169743414 | T | A | 3 | a0001c0001t0001g0203 a0001c0001t0001g0204 a0001c0001t0001g0205 |
3 | HG02280.hp1 HG02723.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.498-1307A>T | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 4/7 | chr4 | 169743414 | |||||||
| chr4:169743626 | T | C | 115 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(112): Show |
181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
intron_variant | MODIFIER | c.498-1519A>G | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 4/7 | chr4 | 169743626 | |||||||
| chr4:169743847 | G | A | 11 | a0001c0001t0001g0004 a0001c0001t0001g0195 a0001c0001t0001g0197 others(8): Show |
17 | HG00639.hp1 HG01884.hp2 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.498-1740C>T | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 4/7 | chr4 | 169743847 | |||||||
| chr4:169743879 | G | GA | 6 | a0001c0001t0001g0169 a0001c0001t0001g0170 a0001c0001t0001g0171 others(3): Show |
6 | HG00099.hp1 HG00099.hp2 HG00642.hp1 others(3): Show |
intron_variant | MODIFIER | c.498-1773dupT | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 4/7 | chr4 | 169743879 | |||||||
| chr4:169744196 | C | T | 3 | a0001c0001t0001g0203 a0001c0001t0001g0204 a0001c0001t0001g0205 |
3 | HG02280.hp1 HG02723.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.498-2089G>A | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 4/7 | chr4 | 169744196 | |||||||
| chr4:169744323 | T | C | 1 | a0001c0001t0001g0174 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.498-2216A>G | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 4/7 | chr4 | 169744323 | |||||||
| chr4:169744590 | A | G | 1 | a0002c0002t0001g0014 | 2 | HG02109.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.498-2483T>C | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 4/7 | chr4 | 169744590 | |||||||
| chr4:169744779 | A | C | 1 | a0001c0001t0001g0191 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.498-2672T>G | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 4/7 | chr4 | 169744779 | |||||||
| chr4:169744810 | T | C | 114 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(111): Show |
180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.498-2703A>G | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 4/7 | chr4 | 169744810 | |||||||
| chr4:169744811 | G | A | 3 | a0001c0001t0002g0192 a0001c0001t0002g0193 a0001c0001t0002g0194 |
3 | HG01358.hp2 HG01891.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.498-2704C>T | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 4/7 | chr4 | 169744811 | |||||||
| chr4:169744819 | C | CT | 6 | a0001c0001t0001g0095 a0001c0001t0001g0127 a0002c0003t0001g0086 others(3): Show |
6 | HG01496.hp2 HG02280.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.498-2713dupA | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 4/7 | chr4 | 169744819 | |||||||
| chr4:169744849 | T | G | 1 | a0001c0001t0001g0175 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.498-2742A>C | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 4/7 | chr4 | 169744849 | |||||||
| chr4:169744960 | T | TAAGAGCA others(3): Show |
187 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(184): Show |
292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.498-2854_498-2853i others(12): Show |
HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 4/7 | chr4 | 169744960 | |||||||
| chr4:169745042 | C | T | 13 | a0001c0001t0001g0004 a0001c0001t0001g0195 a0001c0001t0001g0197 others(10): Show |
21 | HG00639.hp1 HG01884.hp2 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.498-2935G>A | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 4/7 | chr4 | 169745042 | |||||||
| chr4:169745043 | G | A | 114 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(111): Show |
180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.498-2936C>T | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 4/7 | chr4 | 169745043 | |||||||
| chr4:169745044 | G | T | 30 | a0001c0001t0001g0004 a0001c0001t0001g0082 a0001c0001t0001g0100 others(27): Show |
41 | HG00639.hp1 HG01884.hp1 HG01884.hp2 others(38): Show |
intron_variant | MODIFIER | c.498-2937C>A | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 4/7 | chr4 | 169745044 | |||||||
| chr4:169745051 | C | A | 1 | a0001c0004t0001g0020 | 2 | HG01109.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.498-2944G>T | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 4/7 | chr4 | 169745051 | |||||||
| chr4:169745055 | C | T | 3 | a0001c0001t0002g0192 a0001c0001t0002g0193 a0001c0001t0002g0194 |
3 | HG01358.hp2 HG01891.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.498-2948G>A | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 4/7 | chr4 | 169745055 | |||||||
| chr4:169745086 | C | T | 2 | a0002c0003t0001g0086 a0002c0003t0002g0085 |
2 | HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.498-2979G>A | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 4/7 | chr4 | 169745086 | |||||||
| chr4:169745157 | T | C | 3 | a0001c0001t0001g0203 a0001c0001t0001g0204 a0001c0001t0001g0205 |
3 | HG02280.hp1 HG02723.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.498-3050A>G | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 4/7 | chr4 | 169745157 | |||||||
| chr4:169745169 | T | A | 1 | a0001c0001t0002g0192 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.498-3062A>T | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 4/7 | chr4 | 169745169 | |||||||
| chr4:169745304 | T | C | 30 | a0001c0001t0001g0004 a0001c0001t0001g0082 a0001c0001t0001g0100 others(27): Show |
41 | HG00639.hp1 HG01884.hp1 HG01884.hp2 others(38): Show |
intron_variant | MODIFIER | c.498-3197A>G | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 4/7 | chr4 | 169745304 | |||||||
| chr4:169745737 | G | A | 1 | a0001c0001t0001g0176 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.497+3007C>T | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 4/7 | chr4 | 169745737 | |||||||
| chr4:169745940 | A | G | 1 | a0001c0004t0001g0020 | 2 | HG01109.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.497+2804T>C | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 4/7 | chr4 | 169745940 | |||||||
| chr4:169745992 | AC | A | 18 | a0001c0001t0001g0087 a0001c0001t0001g0090 a0001c0001t0001g0095 others(15): Show |
24 | HG01109.hp2 HG02055.hp2 HG02258.hp2 others(21): Show |
intron_variant | MODIFIER | c.497+2751delG | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 4/7 | chr4 | 169745992 | |||||||
| chr4:169746135 | C | A | 1 | a0002c0003t0002g0202 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.497+2609G>T | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 4/7 | chr4 | 169746135 | |||||||
| chr4:169746251 | A | G | 1 | a0001c0001t0001g0189 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.497+2493T>C | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 4/7 | chr4 | 169746251 | |||||||
| chr4:169746318 | C | T | 1 | a0002c0003t0002g0085 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.497+2426G>A | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 4/7 | chr4 | 169746318 | |||||||
| chr4:169746554 | G | T | 1 | a0001c0001t0001g0190 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.497+2190C>A | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 4/7 | chr4 | 169746554 | |||||||
| chr4:169746578 | C | T | 1 | a0002c0003t0002g0085 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.497+2166G>A | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 4/7 | chr4 | 169746578 | |||||||
| chr4:169746693 | T | G | 1 | a0001c0001t0001g0111 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.497+2051A>C | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 4/7 | chr4 | 169746693 | |||||||
| chr4:169746880 | C | T | 163 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(160): Show |
242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
intron_variant | MODIFIER | c.497+1864G>A | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 4/7 | chr4 | 169746880 | |||||||
| chr4:169746881 | AT | A | 13 | a0001c0001t0001g0004 a0001c0001t0001g0195 a0001c0001t0001g0197 others(10): Show |
21 | HG00639.hp1 HG01884.hp2 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.497+1862delA | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 4/7 | chr4 | 169746881 | |||||||
| chr4:169746890 | T | C | 1 | a0001c0001t0001g0190 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.497+1854A>G | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 4/7 | chr4 | 169746890 | |||||||
| chr4:169746923 | TA | T | 17 | a0001c0001t0001g0082 a0001c0001t0001g0100 a0001c0001t0001g0123 others(14): Show |
19 | HG00558.hp1 HG01884.hp1 HG02040.hp2 others(16): Show |
intron_variant | MODIFIER | c.497+1820delT | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 4/7 | chr4 | 169746923 | |||||||
| chr4:169746967 | T | C | 1 | a0001c0001t0001g0177 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.497+1777A>G | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 4/7 | chr4 | 169746967 | |||||||
| chr4:169746985 | C | CT | 13 | a0001c0001t0001g0004 a0001c0001t0001g0195 a0001c0001t0001g0197 others(10): Show |
21 | HG00639.hp1 HG01884.hp2 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.497+1758dupA | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 4/7 | chr4 | 169746985 | |||||||
| chr4:169746990 | T | TA | 3 | a0001c0001t0001g0013 a0001c0001t0001g0179 a0001c0001t0001g0180 |
5 | NA18943.hp1 NA18971.hp2 NA18986.hp1 others(2): Show |
intron_variant | MODIFIER | c.497+1753_497+1754i others(3): Show |
HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 4/7 | chr4 | 169746990 | |||||||
| chr4:169746991 | T | A | 3 | a0001c0001t0001g0013 a0001c0001t0001g0179 a0001c0001t0001g0180 |
5 | NA18943.hp1 NA18971.hp2 NA18986.hp1 others(2): Show |
intron_variant | MODIFIER | c.497+1753A>T | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 4/7 | chr4 | 169746991 | |||||||
| chr4:169746991 | T | TA | 88 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(85): Show |
144 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(141): Show |
intron_variant | MODIFIER | c.497+1752_497+1753i others(3): Show |
HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 4/7 | chr4 | 169746991 | |||||||
| chr4:169746991 | T | TAA | 2 | a0001c0001t0001g0033 a0001c0001t0001g0178 |
3 | HG00280.hp1 HG02004.hp1 HG02027.hp1 |
intron_variant | MODIFIER | c.497+1752_497+1753i others(4): Show |
HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 4/7 | chr4 | 169746991 | |||||||
| chr4:169746992 | T | A | 124 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(121): Show |
195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.497+1752A>T | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 4/7 | chr4 | 169746992 | |||||||
| chr4:169746992 | T | TA | 18 | a0001c0001t0001g0082 a0001c0001t0001g0100 a0001c0001t0001g0107 others(15): Show |
21 | HG01884.hp1 HG02135.hp1 HG02572.hp2 others(18): Show |
intron_variant | MODIFIER | c.497+1751dupT | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 4/7 | chr4 | 169746992 | |||||||
| chr4:169746992 | TA | T | 5 | a0001c0001t0001g0190 a0001c0001t0001g0203 a0001c0004t0001g0020 others(2): Show |
6 | HG01109.hp1 HG03041.hp2 HG03654.hp2 others(3): Show |
intron_variant | MODIFIER | c.497+1751delT | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 4/7 | chr4 | 169746992 | |||||||
| chr4:169746993 | A | T | 1 | a0001c0001t0001g0189 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.497+1751T>A | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 4/7 | chr4 | 169746993 | |||||||
| chr4:169746994 | A | T | 1 | a0001c0004t0001g0020 | 2 | HG01109.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.497+1750T>A | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 4/7 | chr4 | 169746994 | |||||||
| chr4:169747000 | A | G | 13 | a0001c0001t0001g0004 a0001c0001t0001g0195 a0001c0001t0001g0197 others(10): Show |
21 | HG00639.hp1 HG01884.hp2 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.497+1744T>C | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 4/7 | chr4 | 169747000 | |||||||
| chr4:169747002 | A | T | 13 | a0001c0001t0001g0004 a0001c0001t0001g0195 a0001c0001t0001g0197 others(10): Show |
21 | HG00639.hp1 HG01884.hp2 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.497+1742T>A | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 4/7 | chr4 | 169747002 | |||||||
| chr4:169747003 | A | T | 13 | a0001c0001t0001g0004 a0001c0001t0001g0195 a0001c0001t0001g0197 others(10): Show |
21 | HG00639.hp1 HG01884.hp2 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.497+1741T>A | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 4/7 | chr4 | 169747003 | |||||||
| chr4:169747004 | A | C | 13 | a0001c0001t0001g0004 a0001c0001t0001g0195 a0001c0001t0001g0197 others(10): Show |
21 | HG00639.hp1 HG01884.hp2 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.497+1740T>G | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 4/7 | chr4 | 169747004 | |||||||
| chr4:169747105 | G | A | 1 | a0001c0004t0001g0020 | 2 | HG01109.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.497+1639C>T | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 4/7 | chr4 | 169747105 | |||||||
| chr4:169747111 | G | T | 6 | a0001c0004t0001g0019 a0001c0004t0001g0073 a0001c0004t0001g0074 others(3): Show |
7 | HG02572.hp1 HG02615.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.497+1633C>A | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 4/7 | chr4 | 169747111 | |||||||
| chr4:169747190 | A | C | 115 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(112): Show |
181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
intron_variant | MODIFIER | c.497+1554T>G | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 4/7 | chr4 | 169747190 | |||||||
| chr4:169747267 | A | T | 6 | a0001c0001t0001g0012 a0001c0001t0001g0026 a0001c0001t0001g0112 others(3): Show |
9 | HG00140.hp2 HG01261.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.497+1477T>A | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 4/7 | chr4 | 169747267 | |||||||
| chr4:169747287 | T | C | 1 | a0001c0004t0001g0020 | 2 | HG01109.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.497+1457A>G | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 4/7 | chr4 | 169747287 | |||||||
| chr4:169747504 | C | G | 1 | a0001c0001t0001g0111 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.497+1240G>C | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 4/7 | chr4 | 169747504 | |||||||
| chr4:169747805 | C | T | 6 | a0001c0004t0001g0019 a0001c0004t0001g0073 a0001c0004t0001g0074 others(3): Show |
7 | HG02572.hp1 HG02615.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.497+939G>A | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 4/7 | chr4 | 169747805 | |||||||
| chr4:169747841 | G | A | 1 | a0001c0001t0001g0180 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.497+903C>T | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 4/7 | chr4 | 169747841 | |||||||
| chr4:169747877 | C | T | 1 | a0001c0004t0001g0036 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.497+867G>A | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 4/7 | chr4 | 169747877 | |||||||
| chr4:169748087 | C | A | 1 | a0001c0001t0001g0181 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.497+657G>T | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 4/7 | chr4 | 169748087 | |||||||
| chr4:169748096 | A | T | 30 | a0001c0001t0001g0004 a0001c0001t0001g0082 a0001c0001t0001g0100 others(27): Show |
41 | HG00639.hp1 HG01884.hp1 HG01884.hp2 others(38): Show |
intron_variant | MODIFIER | c.497+648T>A | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 4/7 | chr4 | 169748096 | |||||||
| chr4:169748104 | C | T | 1 | a0001c0001t0001g0195 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.497+640G>A | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 4/7 | chr4 | 169748104 | |||||||
| chr4:169748179 | G | T | 1 | a0001c0001t0001g0110 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.497+565C>A | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 4/7 | chr4 | 169748179 | |||||||
| chr4:169748227 | T | A | 1 | a0001c0001t0001g0182 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.497+517A>T | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 4/7 | chr4 | 169748227 | |||||||
| chr4:169748283 | G | T | 13 | a0001c0001t0001g0004 a0001c0001t0001g0195 a0001c0001t0001g0197 others(10): Show |
21 | HG00639.hp1 HG01884.hp2 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.497+461C>A | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 4/7 | chr4 | 169748283 | |||||||
| chr4:169748284 | C | G | 13 | a0001c0001t0001g0004 a0001c0001t0001g0195 a0001c0001t0001g0197 others(10): Show |
21 | HG00639.hp1 HG01884.hp2 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.497+460G>C | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 4/7 | chr4 | 169748284 | |||||||
| chr4:169748420 | C | T | 1 | a0001c0001t0001g0191 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.497+324G>A | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 4/7 | chr4 | 169748420 | |||||||
| chr4:169748433 | C | A | 6 | a0001c0004t0001g0019 a0001c0004t0001g0073 a0001c0004t0001g0074 others(3): Show |
7 | HG02572.hp1 HG02615.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.497+311G>T | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 4/7 | chr4 | 169748433 | |||||||
| chr4:169748465 | T | C | 13 | a0001c0001t0001g0004 a0001c0001t0001g0195 a0001c0001t0001g0197 others(10): Show |
21 | HG00639.hp1 HG01884.hp2 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.497+279A>G | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 4/7 | chr4 | 169748465 | |||||||
| chr4:169748487 | C | T | 5 | a0001c0005t0001g0035 a0001c0005t0001g0206 a0001c0005t0001g0207 others(2): Show |
6 | HG02572.hp2 HG03540.hp1 HG03540.hp2 others(3): Show |
intron_variant | MODIFIER | c.497+257G>A | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 4/7 | chr4 | 169748487 | |||||||
| chr4:169748673 | C | A | 118 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(115): Show |
185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.497+71G>T | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 4/7 | chr4 | 169748673 | |||||||
| chr4:169748699 | T | G | 1 | a0001c0001t0001g0183 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.497+45A>C | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 4/7 | chr4 | 169748699 | |||||||
| chr4:169748980 | C | G | 3 | a0001c0001t0001g0203 a0001c0001t0001g0204 a0001c0001t0001g0205 |
3 | HG02280.hp1 HG02723.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.399-138G>C | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 3/7 | chr4 | 169748980 | |||||||
| chr4:169749086 | T | TA | 11 | a0001c0001t0001g0082 a0001c0001t0001g0100 a0001c0001t0002g0099 others(8): Show |
13 | HG01884.hp1 HG02602.hp2 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.399-245dupT | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 3/7 | chr4 | 169749086 | |||||||
| chr4:169749260 | A | T | 3 | a0001c0001t0001g0087 a0002c0003t0001g0011 a0002c0003t0001g0088 |
5 | NA18939.hp2 NA18964.hp2 NA18977.hp2 others(2): Show |
intron_variant | MODIFIER | c.399-418T>A | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 3/7 | chr4 | 169749260 | |||||||
| chr4:169749408 | TTC | T | 6 | a0001c0001t0001g0004 a0001c0001t0001g0195 a0001c0001t0001g0197 others(3): Show |
13 | HG00639.hp1 HG01884.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.399-568_399-567del others(2): Show |
HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 3/7 | chr4 | 169749408 | |||||||
| chr4:169749441 | T | C | 115 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(112): Show |
181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
intron_variant | MODIFIER | c.399-599A>G | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 3/7 | chr4 | 169749441 | |||||||
| chr4:169749720 | C | CA | 159 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(156): Show |
243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.398+815dupT | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 3/7 | chr4 | 169749720 | |||||||
| chr4:169749720 | C | CAA | 8 | a0001c0001t0001g0095 a0001c0001t0001g0184 a0001c0001t0001g0185 others(5): Show |
8 | HG01074.hp2 HG01891.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.398+814_398+815dup others(2): Show |
HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 3/7 | chr4 | 169749720 | |||||||
| chr4:169749720 | C | CAAAAAA | 7 | a0001c0001t0001g0191 a0001c0004t0001g0019 a0001c0004t0001g0073 others(4): Show |
8 | HG02572.hp1 HG02615.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.398+810_398+815dup others(6): Show |
HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 3/7 | chr4 | 169749720 | |||||||
| chr4:169749795 | T | C | 13 | a0001c0001t0001g0004 a0001c0001t0001g0195 a0001c0001t0001g0197 others(10): Show |
21 | HG00639.hp1 HG01884.hp2 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.398+741A>G | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 3/7 | chr4 | 169749795 | |||||||
| chr4:169750001 | C | A | 115 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(112): Show |
181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
intron_variant | MODIFIER | c.398+535G>T | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 3/7 | chr4 | 169750001 | |||||||
| chr4:169750094 | G | T | 1 | a0001c0001t0001g0191 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.398+442C>A | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 3/7 | chr4 | 169750094 | |||||||
| chr4:169750155 | G | C | 14 | a0001c0001t0001g0004 a0001c0001t0001g0190 a0001c0001t0001g0195 others(11): Show |
22 | HG00639.hp1 HG01884.hp2 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.398+381C>G | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 3/7 | chr4 | 169750155 | |||||||
| chr4:169750238 | G | GGCACCTG others(3): Show |
14 | a0001c0001t0001g0004 a0001c0001t0001g0190 a0001c0001t0001g0195 others(11): Show |
22 | HG00639.hp1 HG01884.hp2 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.398+297_398+298ins others(10): Show |
HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 3/7 | chr4 | 169750238 | |||||||
| chr4:169750240 | C | T | 1 | a0001c0001t0001g0006 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.398+296G>A | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 3/7 | chr4 | 169750240 | |||||||
| chr4:169750312 | G | A | 1 | a0001c0001t0001g0190 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.398+224C>T | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 3/7 | chr4 | 169750312 | |||||||
| chr4:169750505 | G | A | 1 | a0001c0001t0001g0166 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.398+31C>T | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 3/7 | chr4 | 169750505 | |||||||
| chr4:169751055 | C | T | 8 | a0001c0001t0001g0004 a0001c0001t0001g0195 a0001c0001t0001g0197 others(5): Show |
15 | HG00639.hp1 HG01884.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.209-330G>A | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 2/7 | chr4 | 169751055 | |||||||
| chr4:169751241 | A | G | 1 | a0002c0003t0001g0025 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.209-516T>C | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 2/7 | chr4 | 169751241 | |||||||
| chr4:169751259 | C | T | 1 | a0001c0001t0001g0191 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.209-534G>A | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 2/7 | chr4 | 169751259 | |||||||
| chr4:169751275 | C | T | 2 | a0001c0001t0001g0190 a0001c0004t0001g0020 |
3 | HG01109.hp1 HG03654.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.209-550G>A | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 2/7 | chr4 | 169751275 | |||||||
| chr4:169751293 | T | C | 1 | a0001c0004t0001g0020 | 2 | HG01109.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.209-568A>G | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 2/7 | chr4 | 169751293 | |||||||
| chr4:169751351 | C | T | 1 | a0001c0001t0001g0190 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.209-626G>A | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 2/7 | chr4 | 169751351 | |||||||
| chr4:169751360 | G | A | 1 | a0001c0001t0001g0151 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.209-635C>T | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 2/7 | chr4 | 169751360 | |||||||
| chr4:169751402 | C | CA | 29 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(26): Show |
38 | HG00597.hp1 HG00597.hp2 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.209-678dupT | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 2/7 | chr4 | 169751402 | |||||||
| chr4:169751402 | C | CAA | 21 | a0001c0001t0001g0087 a0001c0001t0001g0090 a0001c0001t0001g0095 others(18): Show |
26 | HG01109.hp2 HG02258.hp1 HG02258.hp2 others(23): Show |
intron_variant | MODIFIER | c.209-679_209-678dup others(2): Show |
HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 2/7 | chr4 | 169751402 | |||||||
| chr4:169751510 | T | A | 1 | a0001c0001t0001g0156 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.209-785A>T | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 2/7 | chr4 | 169751510 | |||||||
| chr4:169751741 | G | A | 1 | a0001c0001t0001g0090 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.209-1016C>T | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 2/7 | chr4 | 169751741 | |||||||
| chr4:169751833 | C | T | 1 | a0001c0001t0001g0107 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.209-1108G>A | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 2/7 | chr4 | 169751833 | |||||||
| chr4:169751843 | G | A | 15 | a0001c0001t0001g0082 a0001c0001t0001g0100 a0001c0001t0002g0099 others(12): Show |
18 | HG01884.hp1 HG02572.hp2 HG02602.hp2 others(15): Show |
intron_variant | MODIFIER | c.209-1118C>T | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 2/7 | chr4 | 169751843 | |||||||
| chr4:169751868 | T | A | 8 | a0001c0001t0002g0192 a0001c0001t0002g0193 a0001c0001t0002g0194 others(5): Show |
8 | HG01358.hp2 HG01891.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.209-1143A>T | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 2/7 | chr4 | 169751868 | |||||||
| chr4:169752091 | A | T | 132 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(129): Show |
201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.209-1366T>A | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 2/7 | chr4 | 169752091 | |||||||
| chr4:169752168 | C | CT | 111 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(108): Show |
177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
intron_variant | MODIFIER | c.209-1444dupA | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 2/7 | chr4 | 169752168 | |||||||
| chr4:169752168 | C | CTT | 9 | a0001c0001t0001g0001 a0001c0001t0001g0026 a0001c0001t0001g0114 others(6): Show |
9 | HG02559.hp1 HG03669.hp1 HG03669.hp2 others(6): Show |
intron_variant | MODIFIER | c.209-1445_209-1444d others(4): Show |
HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 2/7 | chr4 | 169752168 | |||||||
| chr4:169752168 | C | CTTT | 16 | a0001c0001t0001g0082 a0001c0001t0001g0100 a0001c0001t0001g0190 others(13): Show |
17 | HG02280.hp1 HG02572.hp2 HG02602.hp2 others(14): Show |
intron_variant | MODIFIER | c.209-1446_209-1444d others(5): Show |
HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 2/7 | chr4 | 169752168 | |||||||
| chr4:169752266 | G | A | 3 | a0002c0002t0002g0057 a0002c0003t0001g0086 a0002c0003t0002g0085 |
3 | HG02723.hp1 HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.208+1410C>T | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 2/7 | chr4 | 169752266 | |||||||
| chr4:169752316 | C | T | 1 | a0001c0004t0001g0020 | 2 | HG01109.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.208+1360G>A | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 2/7 | chr4 | 169752316 | |||||||
| chr4:169752320 | C | T | 16 | a0001c0001t0001g0087 a0001c0001t0001g0095 a0001c0001t0001g0109 others(13): Show |
21 | HG01109.hp2 HG02258.hp2 HG02280.hp2 others(18): Show |
intron_variant | MODIFIER | c.208+1356G>A | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 2/7 | chr4 | 169752320 | |||||||
| chr4:169752397 | C | T | 3 | a0001c0001t0002g0192 a0001c0001t0002g0193 a0001c0001t0002g0194 |
3 | HG01358.hp2 HG01891.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.208+1279G>A | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 2/7 | chr4 | 169752397 | |||||||
| chr4:169752419 | T | A | 10 | a0001c0001t0001g0004 a0001c0001t0001g0195 a0001c0001t0001g0197 others(7): Show |
17 | HG00639.hp1 HG01884.hp2 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.208+1257A>T | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 2/7 | chr4 | 169752419 | |||||||
| chr4:169752473 | T | A | 9 | a0001c0001t0001g0082 a0001c0001t0001g0100 a0001c0001t0002g0099 others(6): Show |
11 | HG01884.hp1 HG02615.hp1 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.208+1203A>T | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 2/7 | chr4 | 169752473 | |||||||
| chr4:169752531 | G | A | 3 | a0001c0001t0002g0192 a0001c0001t0002g0193 a0001c0001t0002g0194 |
3 | HG01358.hp2 HG01891.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.208+1145C>T | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 2/7 | chr4 | 169752531 | |||||||
| chr4:169752555 | A | G | 1 | a0002c0003t0001g0086 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.208+1121T>C | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 2/7 | chr4 | 169752555 | |||||||
| chr4:169752568 | C | T | 1 | a0001c0004t0001g0020 | 2 | HG01109.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.208+1108G>A | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 2/7 | chr4 | 169752568 | |||||||
| chr4:169752587 | T | A | 1 | a0002c0003t0001g0093 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.208+1089A>T | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 2/7 | chr4 | 169752587 | |||||||
| chr4:169752601 | T | A | 1 | a0001c0001t0001g0030 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.208+1075A>T | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 2/7 | chr4 | 169752601 | |||||||
| chr4:169752639 | A | G | 8 | a0001c0001t0002g0192 a0001c0001t0002g0193 a0001c0001t0002g0194 others(5): Show |
8 | HG01358.hp2 HG01891.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.208+1037T>C | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 2/7 | chr4 | 169752639 | |||||||
| chr4:169752695 | C | T | 116 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(113): Show |
182 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(179): Show |
intron_variant | MODIFIER | c.208+981G>A | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 2/7 | chr4 | 169752695 | |||||||
| chr4:169752739 | G | C | 1 | a0001c0001t0001g0030 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.208+937C>G | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 2/7 | chr4 | 169752739 | |||||||
| chr4:169752995 | T | C | 15 | a0001c0001t0001g0082 a0001c0001t0001g0100 a0001c0001t0002g0099 others(12): Show |
18 | HG01884.hp1 HG02572.hp2 HG02602.hp2 others(15): Show |
intron_variant | MODIFIER | c.208+681A>G | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 2/7 | chr4 | 169752995 | |||||||
| chr4:169753028 | G | GT | 41 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(38): Show |
51 | HG00544.hp1 HG00544.hp2 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.208+647dupA | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 2/7 | chr4 | 169753028 | |||||||
| chr4:169753028 | G | GTT | 110 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(107): Show |
167 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(164): Show |
intron_variant | MODIFIER | c.208+646_208+647dup others(2): Show |
HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 2/7 | chr4 | 169753028 | |||||||
| chr4:169753028 | G | GTTT | 23 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(20): Show |
25 | HG00609.hp1 HG00609.hp2 HG01175.hp1 others(22): Show |
intron_variant | MODIFIER | c.208+645_208+647dup others(3): Show |
HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 2/7 | chr4 | 169753028 | |||||||
| chr4:169753028 | G | GTTTTT | 11 | a0001c0001t0001g0100 a0001c0001t0002g0099 a0001c0004t0001g0010 others(8): Show |
13 | HG01884.hp1 HG02602.hp2 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.208+643_208+647dup others(5): Show |
HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 2/7 | chr4 | 169753028 | |||||||
| chr4:169753048 | T | A | 1 | a0004c0008t0001g0108 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.208+628A>T | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 2/7 | chr4 | 169753048 | |||||||
| chr4:169753049 | T | A | 1 | a0004c0008t0001g0108 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.208+627A>T | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 2/7 | chr4 | 169753049 | |||||||
| chr4:169753050 | C | A | 1 | a0004c0008t0001g0108 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.208+626G>T | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 2/7 | chr4 | 169753050 | |||||||
| chr4:169753059 | GGTCTTGC others(148): Show |
G | 1 | a0004c0008t0001g0108 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.208+462_208+616del | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 2/7 | chr4 | 169753059 | |||||||
| chr4:169753185 | C | T | 3 | a0001c0001t0001g0203 a0001c0001t0001g0204 a0001c0001t0001g0205 |
3 | HG02280.hp1 HG02723.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.208+491G>A | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 2/7 | chr4 | 169753185 | |||||||
| chr4:169753365 | C | T | 3 | a0001c0004t0001g0019 a0001c0004t0001g0073 a0001c0004t0001g0074 |
4 | HG02572.hp1 HG02818.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.208+311G>A | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 2/7 | chr4 | 169753365 | |||||||
| chr4:169753486 | T | C | 1 | a0001c0001t0001g0186 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.208+190A>G | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 2/7 | chr4 | 169753486 | |||||||
| chr4:169753658 | G | T | 7 | a0001c0001t0001g0191 a0001c0004t0001g0019 a0001c0004t0001g0073 others(4): Show |
8 | HG02572.hp1 HG02615.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.208+18C>A | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 2/7 | chr4 | 169753658 | |||||||
| chr4:169753924 | A | G | 1 | a0001c0001t0001g0107 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.49-89T>C | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 1/7 | chr4 | 169753924 | |||||||
| chr4:169753938 | T | A | 3 | a0001c0001t0001g0203 a0001c0001t0001g0204 a0001c0001t0001g0205 |
3 | HG02280.hp1 HG02723.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.49-103A>T | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 1/7 | chr4 | 169753938 | |||||||
| chr4:169754495 | C | A | 16 | a0001c0001t0001g0082 a0001c0001t0001g0100 a0001c0001t0002g0099 others(13): Show |
19 | HG01884.hp1 HG02572.hp2 HG02602.hp2 others(16): Show |
intron_variant | MODIFIER | c.49-660G>T | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 1/7 | chr4 | 169754495 | |||||||
| chr4:169754648 | T | C | 3 | a0001c0004t0001g0021 a0002c0002t0001g0078 a0002c0002t0001g0079 |
4 | HG02258.hp1 HG02922.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.49-813A>G | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 1/7 | chr4 | 169754648 | |||||||
| chr4:169754705 | A | G | 1 | a0001c0001t0001g0106 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.49-870T>C | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 1/7 | chr4 | 169754705 | |||||||
| chr4:169754707 | C | T | 1 | a0002c0003t0001g0080 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.49-872G>A | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 1/7 | chr4 | 169754707 | |||||||
| chr4:169754772 | C | T | 1 | a0001c0004t0001g0020 | 2 | HG01109.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.49-937G>A | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 1/7 | chr4 | 169754772 | |||||||
| chr4:169754827 | G | A | 1 | a0002c0003t0001g0025 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.49-992C>T | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 1/7 | chr4 | 169754827 | |||||||
| chr4:169754920 | T | A | 1 | a0002c0003t0001g0098 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.49-1085A>T | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 1/7 | chr4 | 169754920 | |||||||
| chr4:169754944 | G | A | 1 | a0001c0001t0001g0187 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.49-1109C>T | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 1/7 | chr4 | 169754944 | |||||||
| chr4:169755026 | G | A | 1 | a0002c0002t0001g0055 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.49-1191C>T | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 1/7 | chr4 | 169755026 | |||||||
| chr4:169755059 | T | TC | 129 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(126): Show |
197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.49-1225dupG | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 1/7 | chr4 | 169755059 | |||||||
| chr4:169755062 | CCCCG | C | 11 | a0001c0001t0001g0004 a0001c0001t0001g0191 a0001c0001t0001g0195 others(8): Show |
18 | HG00639.hp1 HG01884.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.49-1231_49-1228del others(4): Show |
HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 1/7 | chr4 | 169755062 | |||||||
| chr4:169755065 | CG | C | 18 | a0001c0001t0001g0087 a0001c0001t0001g0090 a0001c0001t0001g0189 others(15): Show |
21 | HG01109.hp2 HG02258.hp2 HG02572.hp2 others(18): Show |
intron_variant | MODIFIER | c.49-1231delC | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 1/7 | chr4 | 169755065 | |||||||
| chr4:169755066 | G | C | 13 | a0001c0001t0001g0095 a0001c0004t0001g0019 a0001c0004t0001g0073 others(10): Show |
13 | HG02055.hp2 HG02280.hp2 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.49-1231C>G | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 1/7 | chr4 | 169755066 | |||||||
| chr4:169755066 | G | T | 134 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(131): Show |
202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.49-1231C>A | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 1/7 | chr4 | 169755066 | |||||||
| chr4:169755069 | C | G | 1 | a0001c0001t0002g0192 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.49-1234G>C | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 1/7 | chr4 | 169755069 | |||||||
| chr4:169755072 | T | C | 21 | a0001c0001t0001g0004 a0001c0001t0001g0191 a0001c0001t0001g0195 others(18): Show |
31 | HG00639.hp1 HG01109.hp1 HG01884.hp2 others(28): Show |
intron_variant | MODIFIER | c.49-1237A>G | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 1/7 | chr4 | 169755072 | |||||||
| chr4:169755136 | G | A | 7 | a0001c0001t0001g0191 a0001c0004t0001g0019 a0001c0004t0001g0073 others(4): Show |
8 | HG02572.hp1 HG02615.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.49-1301C>T | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 1/7 | chr4 | 169755136 | |||||||
| chr4:169755155 | A | G | 122 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(119): Show |
188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.49-1320T>C | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 1/7 | chr4 | 169755155 | |||||||
| chr4:169755163 | A | G | 3 | a0001c0001t0001g0203 a0001c0001t0001g0204 a0001c0001t0001g0205 |
3 | HG02280.hp1 HG02723.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.49-1328T>C | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 1/7 | chr4 | 169755163 | |||||||
| chr4:169755177 | G | A | 114 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(111): Show |
180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.49-1342C>T | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 1/7 | chr4 | 169755177 | |||||||
| chr4:169755223 | T | A | 1 | a0002c0002t0001g0071 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.49-1388A>T | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 1/7 | chr4 | 169755223 | |||||||
| chr4:169755297 | G | C | 1 | a0001c0001t0001g0190 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.49-1462C>G | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 1/7 | chr4 | 169755297 | |||||||
| chr4:169755439 | T | C | 5 | a0001c0001t0001g0188 a0001c0001t0001g0189 a0001c0001t0002g0192 others(2): Show |
5 | HG01358.hp2 HG01891.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.49-1604A>G | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 1/7 | chr4 | 169755439 | |||||||
| chr4:169755631 | T | C | 11 | a0001c0001t0001g0004 a0001c0001t0001g0190 a0001c0001t0001g0195 others(8): Show |
18 | HG00639.hp1 HG01884.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.49-1796A>G | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 1/7 | chr4 | 169755631 | |||||||
| chr4:169755807 | G | A | 2 | a0001c0004t0001g0010 a0001c0004t0001g0072 |
4 | HG01884.hp1 HG02886.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.49-1972C>T | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 1/7 | chr4 | 169755807 | |||||||
| chr4:169756597 | A | T | 3 | a0001c0001t0001g0203 a0001c0001t0001g0204 a0001c0001t0001g0205 |
3 | HG02280.hp1 HG02723.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.48+1233T>A | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 1/7 | chr4 | 169756597 | |||||||
| chr4:169757133 | T | C | 16 | a0001c0001t0001g0004 a0001c0001t0001g0191 a0001c0001t0001g0195 others(13): Show |
23 | HG00639.hp1 HG01358.hp2 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.48+697A>G | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 1/7 | chr4 | 169757133 | |||||||
| chr4:169757219 | C | T | 2 | a0002c0003t0001g0086 a0002c0003t0002g0085 |
2 | HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.48+611G>A | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 1/7 | chr4 | 169757219 | |||||||
| chr4:169757242 | C | T | 2 | a0003c0006t0001g0083 a0003c0006t0001g0084 |
2 | HG02886.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.48+588G>A | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 1/7 | chr4 | 169757242 | |||||||
| chr4:169757354 | A | C | 1 | a0001c0001t0001g0082 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.48+476T>G | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 1/7 | chr4 | 169757354 | |||||||
| chr4:169757531 | G | A | 6 | a0001c0004t0001g0019 a0001c0004t0001g0073 a0001c0004t0001g0074 others(3): Show |
7 | HG02572.hp1 HG02615.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.48+299C>T | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 1/7 | chr4 | 169757531 | |||||||
| chr4:169757571 | AC | A | 7 | a0001c0004t0001g0020 a0001c0005t0001g0035 a0001c0005t0001g0206 others(4): Show |
9 | HG01109.hp1 HG02572.hp2 HG03139.hp1 others(6): Show |
intron_variant | MODIFIER | c.48+258delG | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 1/7 | chr4 | 169757571 | |||||||
| chr4:169757591 | G | T | 1 | a0001c0001t0001g0081 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.48+239C>A | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 1/7 | chr4 | 169757591 | |||||||
| chr4:169757603 | A | C | 6 | a0001c0005t0001g0035 a0001c0005t0001g0206 a0001c0005t0001g0207 others(3): Show |
7 | HG02572.hp2 HG03139.hp1 HG03540.hp1 others(4): Show |
intron_variant | MODIFIER | c.48+227T>G | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 1/7 | chr4 | 169757603 | |||||||
| chr4:169757637 | G | A | 3 | a0001c0004t0001g0021 a0002c0002t0001g0078 a0002c0002t0001g0079 |
4 | HG02258.hp1 HG02922.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.48+193C>T | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 1/7 | chr4 | 169757637 | |||||||
| chr4:169757784 | T | A | 3 | a0001c0001t0001g0203 a0001c0001t0001g0204 a0001c0001t0001g0205 |
3 | HG02280.hp1 HG02723.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.48+46A>T | HPF1 | ENSG00000056050.7 | transcript | ENST00000393381.3 | protein_coding | 1/7 | chr4 | 169757784 |