Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 3249 |
| ensemblid | ENSG00000105707.15 |
| hgncid | 5155 |
| symbol | HPN |
| name | hepsin |
| refseq_nuc | NM_001384133.1 |
| refseq_prot | NP_001371062.1 |
| ensembl_nuc | ENST00000672452.2 |
| ensembl_prot | ENSP00000500664.1 |
| mane_status | MANE Select |
| chr | chr19 |
| start | 35041721 |
| end | 35066573 |
| strand | + |
| ver | v1.2 |
| region | chr19:35041721-35066573 |
| region5000 | chr19:35036721-35071573 |
| regionname0 | HPN_chr19_35041721_35066573 |
| regionname5000 | HPN_chr19_35036721_35071573 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 417 | 380 | 94 | 70 | 154 | 16 | 44 | 113 | HPN_chr19_35036721_35071573 | HPN | MAQKE others(412): Show |
chr19 | 35036721 | 35071573 |
| a0002 | 0/0 | 417 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | HPN_chr19_35036721_35071573 | HPN | MAQKE others(412): Show |
chr19 | 35036721 | 35071573 |
| a0003 | 0/0 | 417 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | MAQKE others(412): Show |
chr19 | 35036721 | 35071573 |
| a0004 | 0/0 | 417 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HPN_chr19_35036721_35071573 | HPN | MAQKE others(412): Show |
chr19 | 35036721 | 35071573 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1251 | 354 | 88 | 63 | 148 | 13 | 41 | HPN_chr19_35036721_35071573 | HPN | ATGGC others(1246): Show |
chr19 | 35036721 | 35071573 | ||
| a0001c0002 | 0/1 | 1251 | 19 | 1 | 7 | 4 | 3 | 3 | HPN_chr19_35036721_35071573 | HPN | ATGGC others(1246): Show |
chr19 | 35036721 | 35071573 | ||
| a0001c0003 | 0/0 | 1251 | 4 | 4 | 0 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | ATGGC others(1246): Show |
chr19 | 35036721 | 35071573 | ||
| a0001c0006 | 0/0 | 1251 | 1 | 0 | 0 | 1 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | ATGGC others(1246): Show |
chr19 | 35036721 | 35071573 | ||
| a0001c0007 | 0/0 | 1251 | 1 | 1 | 0 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | ATGGC others(1246): Show |
chr19 | 35036721 | 35071573 | ||
| a0001c0009 | 0/0 | 1251 | 1 | 0 | 0 | 1 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | ATGGC others(1246): Show |
chr19 | 35036721 | 35071573 | ||
| a0002c0004 | 0/0 | 1251 | 2 | 0 | 0 | 2 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | ATGGC others(1246): Show |
chr19 | 35036721 | 35071573 | ||
| a0003c0005 | 0/0 | 1251 | 1 | 0 | 0 | 1 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | ATGGC others(1246): Show |
chr19 | 35036721 | 35071573 | ||
| a0004c0008 | 0/0 | 1251 | 1 | 0 | 0 | 1 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | ATGGC others(1246): Show |
chr19 | 35036721 | 35071573 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 1746 | 206 | 19 | 53 | 101 | 11 | 22 | HPN_chr19_35036721_35071573 | HPN | GGTGA others(1741): Show |
chr19 | 35036721 | 35071573 |
| a0001c0001t0002 | 1/0 | 1746 | 134 | 56 | 10 | 46 | 2 | 19 | HPN_chr19_35036721_35071573 | HPN | GGTGA others(1741): Show |
chr19 | 35036721 | 35071573 |
| a0001c0001t0003 | 0/0 | 1746 | 8 | 8 | 0 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | GGTGA others(1741): Show |
chr19 | 35036721 | 35071573 |
| a0001c0001t0004 | 0/0 | 1746 | 3 | 3 | 0 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | GGTGA others(1741): Show |
chr19 | 35036721 | 35071573 |
| a0001c0001t0005 | 0/0 | 1746 | 1 | 1 | 0 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | GGTGA others(1741): Show |
chr19 | 35036721 | 35071573 |
| a0001c0001t0006 | 0/0 | 1746 | 1 | 1 | 0 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | GGTGA others(1741): Show |
chr19 | 35036721 | 35071573 |
| a0001c0001t0007 | 0/0 | 1746 | 1 | 0 | 0 | 1 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | GGTGA others(1741): Show |
chr19 | 35036721 | 35071573 |
| a0001c0002t0002 | 0/1 | 1746 | 19 | 1 | 7 | 4 | 3 | 3 | HPN_chr19_35036721_35071573 | HPN | GGTGA others(1741): Show |
chr19 | 35036721 | 35071573 |
| a0001c0003t0002 | 0/0 | 1746 | 4 | 4 | 0 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | GGTGA others(1741): Show |
chr19 | 35036721 | 35071573 |
| a0001c0006t0001 | 0/0 | 1746 | 1 | 0 | 0 | 1 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | GGTGA others(1741): Show |
chr19 | 35036721 | 35071573 |
| a0001c0007t0001 | 0/0 | 1746 | 1 | 1 | 0 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | GGTGA others(1741): Show |
chr19 | 35036721 | 35071573 |
| a0001c0009t0001 | 0/0 | 1746 | 1 | 0 | 0 | 1 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | GGTGA others(1741): Show |
chr19 | 35036721 | 35071573 |
| a0002c0004t0002 | 0/0 | 1746 | 2 | 0 | 0 | 2 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | GGTGA others(1741): Show |
chr19 | 35036721 | 35071573 |
| a0003c0005t0001 | 0/0 | 1746 | 1 | 0 | 0 | 1 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | GGTGA others(1741): Show |
chr19 | 35036721 | 35071573 |
| a0004c0008t0001 | 0/0 | 1746 | 1 | 0 | 0 | 1 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | GGTGA others(1741): Show |
chr19 | 35036721 | 35071573 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0003 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0007 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0009 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0011 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0013 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0016 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0032 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0002g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0002g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0002g0008 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0002g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0002g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0002g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0002g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0002g0025 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0002g0026 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0002g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0002g0028 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0002g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0002g0037 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0002g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0002g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0002g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0002g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0002g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0002g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0002g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0002g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0002g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0002g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0002g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0002g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0002g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0002g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0002g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0002g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0002g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0002g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0002g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0002g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0002g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0002g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0002g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0002g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0002g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0002g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0002g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0002g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0002g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0002g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0002g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0002g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0002g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0002g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0002g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0002g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0002g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0002g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0002g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0002g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0003g0004 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0003g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0003g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0003g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0003g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0004g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0005g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0006g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0001t0007g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0002t0002g0001 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0002t0002g0022 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0002t0002g0050 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0002t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0002t0002g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0002t0002g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0002t0002g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0002t0002g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0002t0002g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0002t0002g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0002t0002g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0002t0002g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0002t0002g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0002t0002g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0003t0002g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0003t0002g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0003t0002g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0003t0002g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0006t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0007t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0001c0009t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0002c0004t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0002c0004t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0003c0005t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| a0004c0008t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0186 | EUR | GBR | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0103 | EUR | GBR | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0075 | EUR | GBR | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0016 | EUR | GBR | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0028 | EUR | FIN | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0016 | EUR | FIN | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0121 | EUR | FIN | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0222 | EUR | FIN | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | CHS | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0154 | EAS | CHS | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | CHS | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0027 | EAS | CHS | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | CHS | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG00438 | hp2 | a0003 | c0005 | t0001 | g0244 | EAS | CHS | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | CHS | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0288 | EAS | CHS | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | CHS | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0088 | EAS | CHS | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | CHS | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | CHS | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | CHS | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | CHS | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0071 | AMR | PUR | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0196 | AMR | PUR | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG00642 | hp2 | a0001 | c0002 | t0002 | g0138 | AMR | PUR | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | CHS | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | CHS | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG00733 | hp1 | a0001 | c0002 | t0002 | g0137 | AMR | PUR | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0227 | AMR | PUR | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0310 | AMR | PUR | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0083 | AMR | PUR | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0195 | AMR | PUR | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0176 | AMR | PUR | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG01070 | hp2 | a0001 | c0002 | t0002 | g0059 | AMR | PUR | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0319 | AMR | PUR | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0201 | AMR | PUR | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | PUR | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0092 | AMR | PUR | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0047 | AMR | PUR | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0287 | AMR | PUR | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG01167 | hp1 | a0001 | c0002 | t0002 | g0143 | AMR | PUR | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | PUR | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG01175 | hp1 | a0001 | c0002 | t0002 | g0122 | AMR | PUR | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0185 | AMR | PUR | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG01192 | hp1 | a0001 | c0002 | t0002 | g0130 | AMR | PUR | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG01255 | hp1 | a0001 | c0002 | t0002 | g0001 | AMR | CLM | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0117 | AMR | CLM | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | CLM | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | CLM | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0188 | AMR | CLM | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | CLM | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0226 | AMR | CLM | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | CLM | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0118 | AMR | CLM | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | CLM | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0217 | AMR | CLM | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0293 | AMR | CLM | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0114 | AMR | CLM | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0291 | AMR | CLM | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | CLM | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | CLM | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG01516 | hp1 | a0001 | c0002 | t0002 | g0144 | EUR | IBS | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0069 | EUR | IBS | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG01517 | hp1 | a0001 | c0002 | t0002 | g0141 | EUR | IBS | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0091 | EUR | IBS | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG01884 | hp1 | a0001 | c0001 | t0005 | g0267 | AFR | ACB | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0262 | AFR | ACB | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0264 | AFR | ACB | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG01891 | hp2 | a0001 | c0001 | t0004 | g0015 | AFR | ACB | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0072 | AMR | PEL | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0221 | AMR | PEL | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0162 | AMR | PEL | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | PEL | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0290 | AMR | PEL | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0109 | AMR | PEL | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | KHV | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0299 | EAS | KHV | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | KHV | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | KHV | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | KHV | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | KHV | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | KHV | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | KHV | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | KHV | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | KHV | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG02080 | hp2 | a0001 | c0006 | t0001 | g0212 | EAS | KHV | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | KHV | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | KHV | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | KHV | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0104 | EAS | KHV | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG02145 | hp1 | a0001 | c0001 | t0003 | g0004 | AFR | ACB | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0181 | AFR | ACB | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | PEL | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0113 | AMR | PEL | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | CDX | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | CDX | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | CDX | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0160 | EAS | CDX | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0131 | AFR | ACB | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0042 | AFR | ACB | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0161 | AFR | ACB | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0120 | AFR | ACB | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0062 | AMR | PEL | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0189 | AFR | ACB | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0045 | AFR | ACB | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0064 | EAS | KHV | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | KHV | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0040 | AFR | GWD | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | GWD | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0156 | SAS | PJL | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0096 | SAS | PJL | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0048 | AFR | GWD | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0324 | AFR | GWD | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0168 | AFR | GWD | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0167 | AFR | GWD | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0030 | AFR | GWD | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | GWD | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0257 | AFR | GWD | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0283 | AFR | GWD | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0300 | SAS | PJL | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0276 | AFR | GWD | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0200 | AFR | GWD | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0322 | AFR | GWD | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0184 | AFR | GWD | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0313 | SAS | PJL | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0294 | SAS | PJL | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0177 | AFR | GWD | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0275 | AFR | GWD | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0272 | AFR | GWD | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0223 | AFR | GWD | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0202 | AFR | GWD | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0206 | AFR | GWD | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0230 | AFR | GWD | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0180 | AFR | GWD | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0220 | AFR | GWD | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0229 | AFR | GWD | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0192 | AFR | ESN | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0046 | AFR | ESN | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG02965 | hp1 | a0001 | c0001 | t0004 | g0015 | AFR | ESN | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0266 | AFR | ESN | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0132 | AFR | ESN | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0053 | AFR | ESN | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG02976 | hp1 | a0001 | c0007 | t0001 | g0281 | AFR | ESN | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0126 | AFR | ESN | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0056 | SAS | PJL | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0084 | SAS | PJL | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0043 | AFR | GWD | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0323 | AFR | GWD | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG03098 | hp1 | a0001 | c0001 | t0003 | g0004 | AFR | MSL | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0041 | AFR | MSL | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | ESN | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0254 | AFR | ESN | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0193 | AFR | ESN | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0284 | AFR | ESN | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG03195 | hp1 | a0001 | c0001 | t0003 | g0049 | AFR | ESN | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0044 | AFR | ESN | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0285 | AFR | MSL | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG03209 | hp2 | a0001 | c0001 | t0003 | g0258 | AFR | MSL | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG03225 | hp1 | a0001 | c0003 | t0002 | g0158 | AFR | MSL | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG03225 | hp2 | a0001 | c0001 | t0003 | g0282 | AFR | MSL | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0081 | SAS | PJL | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0172 | SAS | PJL | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG03453 | hp1 | a0001 | c0003 | t0002 | g0164 | AFR | MSL | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0325 | AFR | MSL | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0231 | AFR | MSL | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | MSL | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0173 | SAS | PJL | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0169 | SAS | PJL | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0170 | SAS | PJL | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0037 | SAS | PJL | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0051 | AFR | ESN | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0256 | AFR | ESN | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0228 | AFR | GWD | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0234 | AFR | MSL | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0248 | AFR | MSL | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0308 | SAS | PJL | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0166 | SAS | PJL | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG03669 | hp1 | a0001 | c0002 | t0002 | g0123 | SAS | PJL | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0008 | SAS | STU | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | STU | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0135 | SAS | PJL | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0187 | SAS | PJL | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG03710 | hp1 | a0001 | c0002 | t0002 | g0140 | SAS | PJL | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0080 | SAS | PJL | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0304 | SAS | BEB | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG03831 | hp2 | a0001 | c0002 | t0002 | g0142 | SAS | BEB | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0279 | SAS | BEB | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0306 | SAS | BEB | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0107 | SAS | BEB | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0025 | SAS | BEB | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0203 | SAS | BEB | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0280 | SAS | STU | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0128 | SAS | STU | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0238 | SAS | BEB | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0133 | SAS | BEB | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0316 | SAS | STU | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0307 | SAS | STU | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0297 | SAS | STU | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0093 | SAS | STU | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0008 | SAS | STU | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0024 | SAS | STU | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | YRI | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| NA18522 | hp2 | a0001 | c0001 | t0003 | g0004 | AFR | YRI | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | CHB | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0125 | EAS | CHB | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0305 | EAS | CHB | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHB | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0255 | AFR | YRI | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0028 | AFR | YRI | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| NA18941 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0239 | EAS | JPT | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| NA18944 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| NA18951 | hp1 | a0004 | c0008 | t0001 | g0205 | EAS | JPT | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0157 | EAS | JPT | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0174 | EAS | JPT | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| NA18956 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0250 | EAS | JPT | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0146 | EAS | JPT | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| NA18967 | hp2 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0270 | EAS | JPT | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0163 | EAS | JPT | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0124 | EAS | JPT | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| NA18997 | hp1 | a0002 | c0004 | t0002 | g0159 | EAS | JPT | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0320 | EAS | JPT | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| NA18998 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| NA19000 | hp2 | a0001 | c0001 | t0007 | g0240 | EAS | JPT | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0147 | EAS | JPT | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| NA19030 | hp1 | a0001 | c0003 | t0002 | g0165 | AFR | LWK | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0274 | AFR | LWK | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| NA19043 | hp1 | a0001 | c0001 | t0004 | g0015 | AFR | LWK | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0253 | AFR | LWK | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| NA19056 | hp1 | a0002 | c0004 | t0002 | g0026 | EAS | JPT | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0292 | EAS | JPT | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0271 | EAS | JPT | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| NA19064 | hp2 | a0001 | c0009 | t0001 | g0006 | EAS | JPT | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| NA19067 | hp2 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| NA19072 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0152 | EAS | JPT | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0235 | EAS | JPT | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| NA19080 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0134 | EAS | JPT | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0153 | EAS | JPT | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0190 | AFR | YRI | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| NA19240 | hp2 | a0001 | c0003 | t0002 | g0273 | AFR | YRI | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0145 | AFR | ASW | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| NA20129 | hp2 | a0001 | c0001 | t0006 | g0073 | AFR | ASW | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0309 | EUR | TSI | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0038 | EUR | TSI | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| NA20805 | hp1 | a0001 | c0002 | t0002 | g0022 | EUR | TSI | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0136 | EUR | TSI | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0097 | SAS | GIH | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0025 | SAS | GIH | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0303 | AMR | CLM | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0249 | AMR | CLM | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0197 | AFR | ACB | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG02109 | hp2 | a0001 | c0001 | t0003 | g0259 | AFR | ACB | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0191 | AFR | ACB | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0224 | AFR | ACB | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG02559 | hp1 | a0001 | c0001 | t0003 | g0004 | AFR | ACB | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0094 | AFR | ACB | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0263 | AFR | MSL | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0052 | AFR | MSL | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0194 | AFR | USA | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| HG06807 | hp2 | a0001 | c0002 | t0002 | g0022 | AFR | USA | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0265 | AFR | USA | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0182 | AFR | USA | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0030 | AFR | LWK | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0321 | AFR | LWK | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0002 | g0050 | REF | REF | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0026 | REF | REF | HPN_chr19_35036721_35071573 | HPN | chr19 | 35036721 | 35071573 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:35059705 | G | C | 1 | a0003 | 1 | HG00438.hp2 | missense_variant | MODERATE | c.193G>C | p.Val65Leu | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 5/13 | 399/1746 | 193/1254 | 65/417 | chr19 | 35059705 | |||
| chr19:35060433 | C | T | 1 | a0004 | 1 | NA18951.hp1 | missense_variant | MODERATE | c.541C>T | p.Arg181Cys | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 8/13 | 747/1746 | 541/1254 | 181/417 | chr19 | 35060433 | |||
| chr19:35065911 | G | A | 1 | a0002 | 2 | NA18997.hp1 NA19056.hp1 |
missense_variant | MODERATE | c.1094G>A | p.Arg365Gln | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 12/13 | 1300/1746 | 1094/1254 | 365/417 | chr19 | 35065911 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:35049336 | C | T | 1 | a0001c0009 | 1 | NA19064.hp2 | synonymous_variant | LOW | c.63C>T | p.Leu21Leu | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 3/13 | 269/1746 | 63/1254 | 21/417 | chr19 | 35049336 | |||
| chr19:35059800 | C | G | 1 | a0001c0003 | 4 | HG03225.hp1 HG03453.hp1 NA19030.hp1 others(1): Show |
splice_region_variant&synonymous_variant | LOW | c.288C>G | p.Leu96Leu | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 5/13 | 494/1746 | 288/1254 | 96/417 | chr19 | 35059800 | |||
| chr19:35059974 | C | T | 1 | a0001c0002 | 18 | HG00642.hp2 HG00733.hp1 HG01070.hp2 others(15): Show |
synonymous_variant | LOW | c.391C>T | p.Leu131Leu | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 6/13 | 597/1746 | 391/1254 | 131/417 | chr19 | 35059974 | |||
| chr19:35060510 | G | A | 1 | a0001c0006 | 1 | HG02080.hp2 | splice_region_variant&synonymous_variant | LOW | c.618G>A | p.Pro206Pro | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 8/13 | 824/1746 | 618/1254 | 206/417 | chr19 | 35060510 | |||
| chr19:35065302 | C | T | 1 | a0001c0007 | 1 | HG02976.hp1 | synonymous_variant | LOW | c.864C>T | p.Gly288Gly | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 10/13 | 1070/1746 | 864/1254 | 288/417 | chr19 | 35065302 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:35041774 | G | A | 2 | a0001c0001t0004 a0001c0001t0005 |
4 | HG01884.hp1 HG01891.hp2 HG02965.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-153G>A | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 1/13 | 733 | chr19 | 35041774 | ||||||
| chr19:35066305 | C | T | 2 | a0001c0001t0003 a0001c0001t0005 |
9 | HG01884.hp1 HG02109.hp2 HG02145.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*18C>T | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 13/13 | 18 | chr19 | 35066305 | ||||||
| chr19:35066333 | G | A | 1 | a0001c0001t0006 | 1 | NA20129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*46G>A | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 13/13 | 46 | chr19 | 35066333 | ||||||
| chr19:35066347 | C | T | 1 | a0001c0001t0007 | 1 | NA19000.hp2 | 3_prime_UTR_variant | MODIFIER | c.*60C>T | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 13/13 | 60 | chr19 | 35066347 | ||||||
| chr19:35066356 | T | G | 8 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0006 others(5): Show |
215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
3_prime_UTR_variant | MODIFIER | c.*69T>G | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 13/13 | 69 | chr19 | 35066356 | ||||||
| chr19:35066536 | C | T | 8 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0006 others(5): Show |
215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
3_prime_UTR_variant | MODIFIER | c.*249C>T | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 13/13 | 249 | chr19 | 35066536 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:35041989 | G | C | 1 | a0001c0001t0001g0039 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-55+117G>C | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 1/12 | chr19 | 35041989 | |||||||
| chr19:35042005 | C | T | 48 | a0001c0001t0001g0016 a0001c0001t0001g0038 a0001c0001t0001g0283 others(45): Show |
52 | HG00140.hp2 HG00280.hp2 HG00544.hp2 others(49): Show |
intron_variant | MODIFIER | c.-55+133C>T | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 1/12 | chr19 | 35042005 | |||||||
| chr19:35042053 | G | A | 2 | a0001c0001t0002g0040 a0001c0001t0002g0041 |
2 | HG02572.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-55+181G>A | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 1/12 | chr19 | 35042053 | |||||||
| chr19:35042263 | G | A | 8 | a0001c0001t0002g0042 a0001c0001t0002g0043 a0001c0001t0002g0044 others(5): Show |
8 | HG01109.hp1 HG02257.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.-54-190G>A | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 1/12 | chr19 | 35042263 | |||||||
| chr19:35042317 | C | T | 2 | a0001c0001t0001g0279 a0001c0001t0002g0280 |
2 | HG03834.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.-54-136C>T | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 1/12 | chr19 | 35042317 | |||||||
| chr19:35042604 | C | T | 1 | a0001c0001t0002g0280 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.16+82C>T | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 2/12 | chr19 | 35042604 | |||||||
| chr19:35042670 | G | A | 1 | a0001c0001t0002g0051 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.16+148G>A | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 2/12 | chr19 | 35042670 | |||||||
| chr19:35042987 | C | T | 2 | a0001c0001t0001g0277 a0001c0001t0001g0278 |
2 | NA18950.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.16+465C>T | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 2/12 | chr19 | 35042987 | |||||||
| chr19:35043217 | G | A | 1 | a0001c0001t0002g0052 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.16+695G>A | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 2/12 | chr19 | 35043217 | |||||||
| chr19:35043251 | AC | A | 3 | a0001c0001t0002g0040 a0001c0001t0002g0041 a0001c0001t0002g0276 |
3 | HG02572.hp1 HG02717.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.16+730delC | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 2/12 | chr19 | 35043251 | |||||||
| chr19:35043265 | T | G | 2 | a0001c0001t0001g0054 a0001c0001t0002g0053 |
2 | HG02970.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.16+743T>G | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 2/12 | chr19 | 35043265 | |||||||
| chr19:35043356 | G | A | 5 | a0001c0001t0001g0283 a0001c0001t0001g0284 a0001c0001t0001g0285 others(2): Show |
5 | HG02647.hp2 HG02976.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.16+834G>A | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 2/12 | chr19 | 35043356 | |||||||
| chr19:35043362 | C | T | 5 | a0001c0001t0001g0275 a0001c0001t0002g0272 a0001c0001t0002g0274 others(2): Show |
8 | HG02145.hp1 HG02559.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.16+840C>T | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 2/12 | chr19 | 35043362 | |||||||
| chr19:35043379 | C | G | 2 | a0001c0001t0002g0270 a0001c0001t0002g0271 |
2 | NA18969.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.16+857C>G | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 2/12 | chr19 | 35043379 | |||||||
| chr19:35043416 | C | A | 5 | a0001c0001t0001g0283 a0001c0001t0001g0284 a0001c0001t0001g0285 others(2): Show |
5 | HG02647.hp2 HG02976.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.16+894C>A | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 2/12 | chr19 | 35043416 | |||||||
| chr19:35043481 | G | A | 25 | a0001c0001t0001g0017 a0001c0001t0001g0055 a0001c0001t0001g0056 others(22): Show |
26 | HG00140.hp1 HG00639.hp2 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.16+959G>A | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 2/12 | chr19 | 35043481 | |||||||
| chr19:35043529 | G | A | 1 | a0001c0001t0002g0276 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.16+1007G>A | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 2/12 | chr19 | 35043529 | |||||||
| chr19:35043551 | G | A | 1 | a0001c0001t0001g0079 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.16+1029G>A | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 2/12 | chr19 | 35043551 | |||||||
| chr19:35043596 | G | A | 1 | a0001c0001t0001g0055 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.16+1074G>A | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 2/12 | chr19 | 35043596 | |||||||
| chr19:35043604 | T | C | 8 | a0001c0001t0001g0275 a0001c0001t0002g0040 a0001c0001t0002g0041 others(5): Show |
11 | HG02145.hp1 HG02559.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.16+1082T>C | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 2/12 | chr19 | 35043604 | |||||||
| chr19:35043808 | C | T | 2 | a0001c0001t0001g0268 a0001c0001t0001g0269 |
2 | NA18972.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.16+1286C>T | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 2/12 | chr19 | 35043808 | |||||||
| chr19:35043911 | T | G | 40 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0019 others(37): Show |
44 | HG00099.hp2 HG00558.hp2 HG00609.hp2 others(41): Show |
intron_variant | MODIFIER | c.16+1389T>G | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 2/12 | chr19 | 35043911 | |||||||
| chr19:35044032 | C | T | 5 | a0001c0001t0002g0051 a0001c0001t0002g0265 a0001c0001t0002g0266 others(2): Show |
7 | HG01884.hp1 HG01891.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.16+1510C>T | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 2/12 | chr19 | 35044032 | |||||||
| chr19:35044064 | T | G | 1 | a0001c0001t0001g0110 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.16+1542T>G | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 2/12 | chr19 | 35044064 | |||||||
| chr19:35044165 | G | A | 1 | a0001c0001t0002g0042 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.16+1643G>A | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 2/12 | chr19 | 35044165 | |||||||
| chr19:35044223 | G | A | 1 | a0001c0001t0001g0080 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.16+1701G>A | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 2/12 | chr19 | 35044223 | |||||||
| chr19:35044237 | G | C | 1 | a0001c0001t0002g0042 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.16+1715G>C | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 2/12 | chr19 | 35044237 | |||||||
| chr19:35044385 | A | G | 132 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(129): Show |
141 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(138): Show |
intron_variant | MODIFIER | c.16+1863A>G | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 2/12 | chr19 | 35044385 | |||||||
| chr19:35044396 | C | T | 1 | a0001c0001t0002g0109 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.16+1874C>T | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 2/12 | chr19 | 35044396 | |||||||
| chr19:35044428 | C | T | 61 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0019 others(58): Show |
65 | HG00099.hp2 HG00558.hp2 HG00609.hp2 others(62): Show |
intron_variant | MODIFIER | c.16+1906C>T | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 2/12 | chr19 | 35044428 | |||||||
| chr19:35044827 | C | T | 1 | a0001c0001t0001g0252 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.16+2305C>T | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 2/12 | chr19 | 35044827 | |||||||
| chr19:35044848 | C | T | 1 | a0001c0001t0001g0108 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.16+2326C>T | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 2/12 | chr19 | 35044848 | |||||||
| chr19:35044872 | C | T | 2 | a0001c0001t0004g0015 a0001c0001t0005g0267 |
4 | HG01884.hp1 HG01891.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.16+2350C>T | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 2/12 | chr19 | 35044872 | |||||||
| chr19:35044886 | C | T | 1 | a0001c0001t0002g0266 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.16+2364C>T | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 2/12 | chr19 | 35044886 | |||||||
| chr19:35044887 | G | A | 1 | a0001c0001t0002g0053 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.16+2365G>A | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 2/12 | chr19 | 35044887 | |||||||
| chr19:35044920 | C | T | 3 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0001t0002g0250 |
3 | NA18957.hp2 NA19072.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.16+2398C>T | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 2/12 | chr19 | 35044920 | |||||||
| chr19:35044959 | C | T | 1 | a0001c0001t0001g0285 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.16+2437C>T | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 2/12 | chr19 | 35044959 | |||||||
| chr19:35045092 | G | A | 14 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0021 others(11): Show |
18 | HG00738.hp2 HG01069.hp2 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.16+2570G>A | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 2/12 | chr19 | 35045092 | |||||||
| chr19:35045277 | C | T | 5 | a0001c0001t0001g0249 a0001c0001t0001g0275 a0001c0001t0002g0248 others(2): Show |
8 | HG01123.hp2 HG02145.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.16+2755C>T | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 2/12 | chr19 | 35045277 | |||||||
| chr19:35045363 | G | A | 1 | a0001c0001t0001g0287 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.16+2841G>A | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 2/12 | chr19 | 35045363 | |||||||
| chr19:35045460 | G | A | 28 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0056 others(25): Show |
38 | HG00323.hp1 HG00741.hp1 HG00741.hp2 others(35): Show |
intron_variant | MODIFIER | c.16+2938G>A | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 2/12 | chr19 | 35045460 | |||||||
| chr19:35045464 | C | T | 1 | a0001c0001t0002g0109 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.16+2942C>T | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 2/12 | chr19 | 35045464 | |||||||
| chr19:35045466 | C | T | 1 | a0001c0001t0001g0036 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.16+2944C>T | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 2/12 | chr19 | 35045466 | |||||||
| chr19:35045512 | A | G | 1 | a0001c0001t0001g0320 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.16+2990A>G | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 2/12 | chr19 | 35045512 | |||||||
| chr19:35045648 | G | A | 10 | a0001c0001t0001g0017 a0001c0001t0001g0057 a0001c0001t0001g0058 others(7): Show |
11 | HG00544.hp2 HG02015.hp1 HG02040.hp2 others(8): Show |
intron_variant | MODIFIER | c.16+3126G>A | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 2/12 | chr19 | 35045648 | |||||||
| chr19:35045650 | C | CGCCTGTC others(62): Show |
4 | a0001c0001t0002g0131 a0001c0001t0002g0132 a0001c0001t0002g0276 others(1): Show |
4 | HG01192.hp1 HG02257.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.16+3178_16+3246dup others(69): Show |
HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 35045650 | ||||||
| chr19:35045650 | C | CGCCTGTC others(62): Show |
1 | a0001c0001t0002g0238 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.16+3177_16+3178ins others(69): Show |
HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 35045650 | ||||||
| chr19:35045650 | CGCCTGTC others(62): Show |
C | 33 | a0001c0001t0001g0005 a0001c0001t0001g0019 a0001c0001t0001g0034 others(30): Show |
41 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(38): Show |
intron_variant | MODIFIER | c.16+3178_16+3246del others(69): Show |
HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 35045650 | ||||||
| chr19:35045690 | G | A | 1 | a0001c0001t0001g0018 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.16+3168G>A | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 2/12 | chr19 | 35045690 | |||||||
| chr19:35045700 | C | G | 10 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0203 others(7): Show |
10 | HG00280.hp2 HG00609.hp1 HG00621.hp1 others(7): Show |
intron_variant | MODIFIER | c.16+3178C>G | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 2/12 | chr19 | 35045700 | |||||||
| chr19:35045700 | CTGGGCCA others(62): Show |
C | 13 | a0001c0001t0001g0012 a0001c0001t0001g0071 a0001c0001t0001g0296 others(10): Show |
13 | HG00639.hp2 HG02622.hp2 HG02818.hp1 others(10): Show |
intron_variant | MODIFIER | c.16+3217_16+3285del others(69): Show |
HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 35045700 | ||||||
| chr19:35045769 | G | C | 2 | a0001c0001t0002g0120 a0001c0001t0002g0262 |
2 | HG01884.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.16+3247G>C | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 2/12 | chr19 | 35045769 | |||||||
| chr19:35045780 | G | A | 11 | a0001c0001t0001g0017 a0001c0001t0001g0057 a0001c0001t0001g0058 others(8): Show |
12 | HG00544.hp2 HG02015.hp1 HG02040.hp2 others(9): Show |
intron_variant | MODIFIER | c.16+3258G>A | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 2/12 | chr19 | 35045780 | |||||||
| chr19:35046247 | A | AT | 16 | a0001c0001t0001g0017 a0001c0001t0001g0057 a0001c0001t0001g0086 others(13): Show |
17 | HG00438.hp1 HG01884.hp2 HG02040.hp2 others(14): Show |
intron_variant | MODIFIER | c.17-3028dupT | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 35046247 | ||||||
| chr19:35046247 | A | ATT | 90 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(87): Show |
104 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.17-3029_17-3028dup others(2): Show |
HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 35046247 | ||||||
| chr19:35046247 | AT | A | 6 | a0001c0001t0001g0055 a0001c0001t0001g0135 a0001c0001t0001g0268 others(3): Show |
6 | HG00323.hp1 HG02976.hp1 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.17-3028delT | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 35046247 | ||||||
| chr19:35046305 | C | T | 201 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(198): Show |
229 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.17-2985C>T | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 2/12 | chr19 | 35046305 | |||||||
| chr19:35046389 | C | T | 1 | a0001c0001t0001g0312 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.17-2901C>T | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 2/12 | chr19 | 35046389 | |||||||
| chr19:35046390 | G | A | 3 | a0001c0001t0001g0095 a0001c0002t0002g0122 a0001c0002t0002g0123 |
3 | HG01175.hp1 HG03669.hp1 NA18953.hp2 |
intron_variant | MODIFIER | c.17-2900G>A | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 2/12 | chr19 | 35046390 | |||||||
| chr19:35046528 | A | T | 1 | a0001c0001t0001g0057 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.17-2762A>T | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 2/12 | chr19 | 35046528 | |||||||
| chr19:35046659 | A | G | 1 | a0001c0001t0002g0030 | 2 | HG02630.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.17-2631A>G | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 2/12 | chr19 | 35046659 | |||||||
| chr19:35046802 | G | A | 13 | a0001c0001t0001g0136 a0001c0001t0001g0139 a0001c0002t0002g0001 others(10): Show |
18 | HG00639.hp1 HG00642.hp2 HG00733.hp1 others(15): Show |
intron_variant | MODIFIER | c.17-2488G>A | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 2/12 | chr19 | 35046802 | |||||||
| chr19:35046822 | G | GTATT | 16 | a0001c0001t0001g0136 a0001c0001t0001g0139 a0001c0001t0002g0120 others(13): Show |
21 | HG00639.hp1 HG00642.hp2 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.17-2450_17-2447dup others(4): Show |
HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 35046822 | ||||||
| chr19:35046840 | A | T | 1 | a0001c0001t0001g0247 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.17-2450A>T | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 2/12 | chr19 | 35046840 | |||||||
| chr19:35046845 | T | C | 1 | a0001c0001t0001g0314 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.17-2445T>C | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 2/12 | chr19 | 35046845 | |||||||
| chr19:35046953 | C | T | 1 | a0001c0001t0001g0054 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.17-2337C>T | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 2/12 | chr19 | 35046953 | |||||||
| chr19:35047018 | C | T | 1 | a0001c0001t0002g0263 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.17-2272C>T | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 2/12 | chr19 | 35047018 | |||||||
| chr19:35047271 | C | T | 3 | a0001c0001t0001g0033 a0001c0001t0001g0236 a0001c0001t0001g0237 |
4 | NA19011.hp1 NA19057.hp2 NA19067.hp1 others(1): Show |
intron_variant | MODIFIER | c.17-2019C>T | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 2/12 | chr19 | 35047271 | |||||||
| chr19:35047333 | C | T | 1 | a0001c0001t0001g0054 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.17-1957C>T | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 2/12 | chr19 | 35047333 | |||||||
| chr19:35047563 | C | T | 1 | a0001c0001t0001g0237 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.17-1727C>T | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 2/12 | chr19 | 35047563 | |||||||
| chr19:35047591 | G | A | 5 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0002g0107 others(2): Show |
5 | HG02071.hp2 HG03927.hp2 HG04115.hp1 others(2): Show |
intron_variant | MODIFIER | c.17-1699G>A | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 2/12 | chr19 | 35047591 | |||||||
| chr19:35047624 | C | T | 7 | a0001c0001t0001g0039 a0001c0001t0001g0245 a0001c0001t0001g0246 others(4): Show |
7 | HG02027.hp2 NA18950.hp2 NA18982.hp2 others(4): Show |
intron_variant | MODIFIER | c.17-1666C>T | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 2/12 | chr19 | 35047624 | |||||||
| chr19:35047636 | A | ACCTG | 52 | a0001c0001t0001g0011 a0001c0001t0001g0023 a0001c0001t0001g0055 others(49): Show |
55 | HG00099.hp1 HG00423.hp1 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.17-1654_17-1653ins others(4): Show |
HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 2/12 | chr19 | 35047636 | |||||||
| chr19:35047637 | G | T | 52 | a0001c0001t0001g0011 a0001c0001t0001g0023 a0001c0001t0001g0055 others(49): Show |
55 | HG00099.hp1 HG00423.hp1 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.17-1653G>T | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 2/12 | chr19 | 35047637 | |||||||
| chr19:35047644 | G | A | 87 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(84): Show |
101 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(98): Show |
intron_variant | MODIFIER | c.17-1646G>A | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 2/12 | chr19 | 35047644 | |||||||
| chr19:35047648 | C | T | 1 | a0001c0001t0001g0203 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.17-1642C>T | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 2/12 | chr19 | 35047648 | |||||||
| chr19:35048006 | AAAAG | A | 5 | a0001c0001t0001g0023 a0001c0001t0001g0127 a0001c0001t0001g0186 others(2): Show |
6 | HG00099.hp1 HG01099.hp2 HG01123.hp1 others(3): Show |
intron_variant | MODIFIER | c.17-1278_17-1275del others(4): Show |
HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 35048006 | ||||||
| chr19:35048024 | G | GAGAAGAA others(4): Show |
11 | a0001c0001t0001g0017 a0001c0001t0001g0024 a0001c0001t0001g0029 others(8): Show |
14 | HG03654.hp1 HG03669.hp2 HG03942.hp2 others(11): Show |
intron_variant | MODIFIER | c.17-1262_17-1261ins others(11): Show |
HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 35048024 | ||||||
| chr19:35048026 | G | A | 1 | a0001c0001t0002g0100 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.17-1264G>A | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 2/12 | chr19 | 35048026 | |||||||
| chr19:35048026 | G | GA | 22 | a0001c0001t0001g0019 a0001c0001t0001g0060 a0001c0001t0001g0063 others(19): Show |
25 | HG00099.hp2 HG00621.hp2 HG00735.hp1 others(22): Show |
intron_variant | MODIFIER | c.17-1259dupA | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 35048026 | ||||||
| chr19:35048028 | A | AAAAAG | 6 | a0001c0001t0001g0016 a0001c0001t0001g0038 a0001c0001t0002g0061 others(3): Show |
9 | HG00140.hp2 HG00280.hp2 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.17-1259_17-1258ins others(5): Show |
HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 35048028 | ||||||
| chr19:35048028 | A | AAAAAGAA others(2): Show |
9 | a0001c0001t0001g0009 a0001c0001t0001g0135 a0001c0001t0001g0151 others(6): Show |
14 | HG00558.hp2 HG00609.hp2 HG01192.hp2 others(11): Show |
intron_variant | MODIFIER | c.17-1259_17-1258ins others(9): Show |
HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 35048028 | ||||||
| chr19:35048028 | A | AAAAAGAA others(6): Show |
13 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0080 others(10): Show |
16 | HG00408.hp2 HG00438.hp1 HG00738.hp1 others(13): Show |
intron_variant | MODIFIER | c.17-1259_17-1258ins others(13): Show |
HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 35048028 | ||||||
| chr19:35048028 | A | AAAAG | 11 | a0001c0001t0001g0139 a0001c0001t0002g0008 a0001c0001t0002g0083 others(8): Show |
13 | HG00639.hp1 HG00741.hp1 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.17-1210_17-1207dup others(4): Show |
HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 35048028 | ||||||
| chr19:35048028 | A | AAAAGAAA others(1): Show |
3 | a0001c0001t0002g0125 a0001c0002t0002g0130 a0001c0002t0002g0144 |
3 | HG01192.hp1 HG01516.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.17-1214_17-1207dup others(8): Show |
HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 35048028 | ||||||
| chr19:35048028 | A | AAAAGAAA others(5): Show |
1 | a0001c0001t0002g0322 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.17-1218_17-1207dup others(12): Show |
HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 35048028 | ||||||
| chr19:35048028 | A | AAAAGAAA others(13): Show |
2 | a0001c0001t0002g0169 a0001c0001t0002g0170 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.17-1226_17-1207dup others(20): Show |
HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 35048028 | ||||||
| chr19:35048028 | A | AAAAGAAA others(25): Show |
1 | a0001c0001t0001g0301 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.17-1238_17-1207dup others(32): Show |
HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 35048028 | ||||||
| chr19:35048028 | A | AAAGAAAG others(4): Show |
1 | a0001c0001t0002g0197 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.17-1260_17-1259ins others(11): Show |
HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 35048028 | ||||||
| chr19:35048028 | A | AG | 40 | a0001c0001t0001g0032 a0001c0001t0001g0036 a0001c0001t0001g0057 others(37): Show |
42 | HG00140.hp1 HG00408.hp1 HG00733.hp2 others(39): Show |
intron_variant | MODIFIER | c.17-1262_17-1261ins others(1): Show |
HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 2/12 | chr19 | 35048028 | |||||||
| chr19:35048028 | A | AGAAAG | 25 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0013 others(22): Show |
30 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(27): Show |
intron_variant | MODIFIER | c.17-1262_17-1261ins others(5): Show |
HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 2/12 | chr19 | 35048028 | |||||||
| chr19:35048028 | A | AGAAAGAA others(2): Show |
26 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0031 others(23): Show |
32 | HG00438.hp2 HG00673.hp1 HG00673.hp2 others(29): Show |
intron_variant | MODIFIER | c.17-1262_17-1261ins others(9): Show |
HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 2/12 | chr19 | 35048028 | |||||||
| chr19:35048028 | A | AGAAAGAA others(8): Show |
1 | a0001c0001t0001g0198 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.17-1262_17-1261ins others(15): Show |
HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 2/12 | chr19 | 35048028 | |||||||
| chr19:35048028 | A | AGAAAGAA others(12): Show |
2 | a0001c0001t0001g0018 a0001c0001t0001g0199 |
3 | NA19005.hp2 NA19066.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.17-1262_17-1261ins others(19): Show |
HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 2/12 | chr19 | 35048028 | |||||||
| chr19:35048028 | A | AGAAAGAA others(6): Show |
13 | a0001c0001t0001g0007 a0001c0001t0001g0077 a0001c0001t0001g0119 others(10): Show |
15 | HG00323.hp2 HG00735.hp2 HG01123.hp2 others(12): Show |
intron_variant | MODIFIER | c.17-1262_17-1261ins others(13): Show |
HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 2/12 | chr19 | 35048028 | |||||||
| chr19:35048028 | A | G | 3 | a0001c0001t0002g0131 a0001c0001t0002g0132 a0001c0001t0002g0235 |
3 | HG02257.hp1 HG02970.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.17-1262A>G | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 2/12 | chr19 | 35048028 | |||||||
| chr19:35048028 | AAAAG | A | 6 | a0001c0001t0001g0136 a0001c0001t0002g0124 a0001c0002t0002g0059 others(3): Show |
6 | HG00733.hp1 HG01070.hp2 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.17-1210_17-1207del others(4): Show |
HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 35048028 | ||||||
| chr19:35048057 | AAAGAAAG others(8): Show |
A | 1 | a0001c0001t0002g0053 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.17-1230_17-1216del others(15): Show |
HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 35048057 | ||||||
| chr19:35048057 | AAAGAAAG others(12): Show |
A | 4 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0002g0107 others(1): Show |
4 | HG02071.hp2 HG03927.hp2 NA18960.hp2 others(1): Show |
intron_variant | MODIFIER | c.17-1230_17-1212del others(19): Show |
HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 35048057 | ||||||
| chr19:35048060 | G | C | 1 | a0001c0001t0001g0079 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.17-1230G>C | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 2/12 | chr19 | 35048060 | |||||||
| chr19:35048061 | AAAGAAAG others(4): Show |
A | 7 | a0001c0001t0002g0274 a0001c0001t0003g0004 a0001c0001t0003g0049 others(4): Show |
10 | HG01884.hp1 HG02109.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.17-1226_17-1216del others(11): Show |
HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 35048061 | ||||||
| chr19:35048061 | AAAGAAAG others(8): Show |
A | 3 | a0001c0001t0002g0172 a0001c0001t0002g0255 a0001c0001t0002g0280 |
3 | HG03239.hp2 HG04115.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.17-1226_17-1212del others(15): Show |
HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 35048061 | ||||||
| chr19:35048065 | AAAGAAAG others(4): Show |
A | 1 | a0001c0001t0002g0126 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.17-1222_17-1212del others(11): Show |
HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 35048065 | ||||||
| chr19:35048069 | AAAGAAAG | A | 3 | a0001c0001t0002g0174 a0001c0001t0002g0257 a0001c0001t0002g0266 |
3 | HG02647.hp1 HG02965.hp2 NA18954.hp2 |
intron_variant | MODIFIER | c.17-1218_17-1212del others(7): Show |
HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 35048069 | ||||||
| chr19:35048072 | G | GA | 8 | a0001c0001t0002g0028 a0001c0001t0002g0052 a0001c0001t0002g0196 others(5): Show |
9 | HG00280.hp1 HG00642.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.17-1215dupA | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 35048072 | ||||||
| chr19:35048073 | AAAG | A | 5 | a0001c0001t0001g0171 a0001c0001t0002g0027 a0001c0001t0002g0173 others(2): Show |
6 | HG00423.hp2 HG01884.hp2 HG02129.hp1 others(3): Show |
intron_variant | MODIFIER | c.17-1214_17-1212del others(3): Show |
HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 35048073 | ||||||
| chr19:35048077 | A | G | 19 | a0001c0001t0002g0028 a0001c0001t0002g0030 a0001c0001t0002g0052 others(16): Show |
24 | HG00280.hp1 HG00323.hp1 HG00642.hp1 others(21): Show |
intron_variant | MODIFIER | c.17-1213A>G | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 2/12 | chr19 | 35048077 | |||||||
| chr19:35048079 | A | AAG | 3 | a0001c0001t0002g0156 a0001c0001t0002g0189 a0001c0001t0002g0190 |
3 | HG02451.hp1 HG02602.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.17-1211_17-1210ins others(2): Show |
HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 2/12 | chr19 | 35048079 | |||||||
| chr19:35048080 | G | A | 27 | a0001c0001t0001g0017 a0001c0001t0001g0024 a0001c0001t0001g0070 others(24): Show |
33 | HG01106.hp2 HG01891.hp2 HG02071.hp1 others(30): Show |
intron_variant | MODIFIER | c.17-1210G>A | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 2/12 | chr19 | 35048080 | |||||||
| chr19:35048080 | GA | G | 35 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0171 others(32): Show |
41 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(38): Show |
intron_variant | MODIFIER | c.17-1206delA | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 35048080 | ||||||
| chr19:35048081 | A | G | 10 | a0001c0001t0002g0010 a0001c0001t0002g0043 a0001c0001t0002g0092 others(7): Show |
12 | HG01106.hp2 HG02071.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.17-1209A>G | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 2/12 | chr19 | 35048081 | |||||||
| chr19:35048082 | A | AAAAAGG | 118 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(115): Show |
147 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.17-1206_17-1205ins others(6): Show |
HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 35048082 | ||||||
| chr19:35048082 | A | AAAGG | 11 | a0001c0001t0002g0037 a0001c0001t0002g0147 a0001c0001t0002g0157 others(8): Show |
12 | HG02109.hp1 HG02486.hp1 HG02886.hp2 others(9): Show |
intron_variant | MODIFIER | c.17-1193_17-1190dup others(4): Show |
HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 35048082 | ||||||
| chr19:35048082 | A | AAGAAAAG others(1): Show |
11 | a0001c0001t0001g0055 a0001c0001t0002g0045 a0001c0001t0002g0051 others(8): Show |
11 | HG01978.hp2 HG02148.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.17-1207_17-1206ins others(8): Show |
HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 35048082 | ||||||
| chr19:35048082 | A | AAGAAAGA others(5): Show |
11 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0175 others(8): Show |
11 | HG02572.hp1 HG02738.hp2 HG02922.hp2 others(8): Show |
intron_variant | MODIFIER | c.17-1207_17-1206ins others(12): Show |
HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 35048082 | ||||||
| chr19:35048082 | A | AAGAAAGA others(9): Show |
12 | a0001c0001t0001g0011 a0001c0001t0001g0067 a0001c0001t0001g0176 others(9): Show |
14 | HG01070.hp1 HG01071.hp1 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.17-1207_17-1206ins others(16): Show |
HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 35048082 | ||||||
| chr19:35048082 | A | AAGAAAGA others(15): Show |
18 | a0001c0001t0001g0063 a0001c0001t0001g0075 a0001c0001t0001g0085 others(15): Show |
18 | HG00140.hp1 HG00621.hp2 HG01074.hp2 others(15): Show |
intron_variant | MODIFIER | c.17-1207_17-1206ins others(22): Show |
HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 35048082 | ||||||
| chr19:35048082 | A | AAGAAAGA others(13): Show |
14 | a0001c0001t0001g0023 a0001c0001t0001g0111 a0001c0001t0001g0178 others(11): Show |
15 | HG00099.hp1 HG00423.hp1 HG01123.hp1 others(12): Show |
intron_variant | MODIFIER | c.17-1207_17-1206ins others(20): Show |
HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 35048082 | ||||||
| chr19:35048082 | A | AAGAAAGA others(19): Show |
10 | a0001c0001t0001g0082 a0001c0001t0001g0097 a0001c0001t0001g0098 others(7): Show |
10 | HG00741.hp2 HG01258.hp1 HG01361.hp1 others(7): Show |
intron_variant | MODIFIER | c.17-1207_17-1206ins others(26): Show |
HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 35048082 | ||||||
| chr19:35048082 | A | AAGAAAGA others(17): Show |
16 | a0001c0001t0001g0054 a0001c0001t0001g0068 a0001c0001t0001g0148 others(13): Show |
16 | HG01175.hp2 HG02027.hp1 HG02083.hp1 others(13): Show |
intron_variant | MODIFIER | c.17-1207_17-1206ins others(24): Show |
HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 35048082 | ||||||
| chr19:35048082 | A | AAGAAAGA others(23): Show |
4 | a0001c0001t0001g0072 a0001c0001t0001g0227 a0001c0001t0001g0241 others(1): Show |
4 | HG00733.hp2 HG01975.hp2 HG02083.hp2 others(1): Show |
intron_variant | MODIFIER | c.17-1207_17-1206ins others(30): Show |
HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 35048082 | ||||||
| chr19:35048082 | A | AAGAAAGA others(25): Show |
1 | a0001c0001t0001g0127 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.17-1207_17-1206ins others(32): Show |
HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 35048082 | ||||||
| chr19:35048082 | A | AAGAAAGA others(31): Show |
1 | a0001c0001t0001g0202 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.17-1207_17-1206ins others(38): Show |
HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 35048082 | ||||||
| chr19:35048082 | A | AAGAAAGA others(29): Show |
1 | a0001c0001t0001g0320 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.17-1207_17-1206ins others(36): Show |
HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 35048082 | ||||||
| chr19:35048082 | A | AAGAAAGA others(16): Show |
1 | a0001c0001t0001g0302 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.17-1207_17-1206ins others(23): Show |
HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 35048082 | ||||||
| chr19:35048082 | A | AAGAAAGA others(21): Show |
1 | a0001c0001t0001g0188 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.17-1207_17-1206ins others(28): Show |
HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 35048082 | ||||||
| chr19:35048082 | A | AGG | 19 | a0001c0001t0001g0017 a0001c0001t0001g0024 a0001c0001t0001g0070 others(16): Show |
23 | HG01891.hp2 HG02074.hp2 HG02155.hp2 others(20): Show |
intron_variant | MODIFIER | c.17-1208_17-1207ins others(2): Show |
HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 2/12 | chr19 | 35048082 | |||||||
| chr19:35048082 | A | G | 45 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0171 others(42): Show |
53 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(50): Show |
intron_variant | MODIFIER | c.17-1208A>G | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 2/12 | chr19 | 35048082 | |||||||
| chr19:35048411 | C | T | 1 | a0001c0001t0002g0100 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.17-879C>T | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 2/12 | chr19 | 35048411 | |||||||
| chr19:35048813 | G | A | 2 | a0001c0001t0002g0121 a0001c0001t0002g0156 |
2 | HG00323.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.17-477G>A | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 2/12 | chr19 | 35048813 | |||||||
| chr19:35049071 | C | G | 2 | a0001c0001t0001g0075 a0001c0001t0001g0319 |
2 | HG00140.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.17-219C>G | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 2/12 | chr19 | 35049071 | |||||||
| chr19:35049099 | G | A | 1 | a0001c0001t0001g0054 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.17-191G>A | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 2/12 | chr19 | 35049099 | |||||||
| chr19:35049222 | C | T | 1 | a0001c0001t0001g0213 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.17-68C>T | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 2/12 | chr19 | 35049222 | |||||||
| chr19:35049462 | C | T | 1 | a0001c0001t0002g0191 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.119-13C>T | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 3/12 | chr19 | 35049462 | |||||||
| chr19:35049563 | G | A | 1 | a0001c0001t0002g0231 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.160+47G>A | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 4/12 | chr19 | 35049563 | |||||||
| chr19:35049589 | G | A | 6 | a0001c0001t0002g0043 a0001c0001t0002g0126 a0001c0001t0002g0161 others(3): Show |
6 | HG02258.hp1 HG02647.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.160+73G>A | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 4/12 | chr19 | 35049589 | |||||||
| chr19:35049853 | TTTTG | T | 49 | a0001c0001t0001g0011 a0001c0001t0001g0023 a0001c0001t0001g0055 others(46): Show |
52 | HG00099.hp1 HG00423.hp1 HG01070.hp1 others(49): Show |
intron_variant | MODIFIER | c.160+345_160+348del others(4): Show |
HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr19 | 35049853 | ||||||
| chr19:35049857 | G | T | 2 | a0001c0001t0002g0052 a0001c0001t0002g0325 |
2 | HG03453.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.160+341G>T | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 4/12 | chr19 | 35049857 | |||||||
| chr19:35049861 | G | GT | 6 | a0001c0001t0002g0053 a0001c0001t0003g0004 a0001c0001t0003g0049 others(3): Show |
7 | HG00733.hp1 HG02559.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.160+360dupT | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr19 | 35049861 | ||||||
| chr19:35049861 | G | T | 17 | a0001c0001t0002g0028 a0001c0001t0002g0030 a0001c0001t0002g0052 others(14): Show |
19 | HG00280.hp1 HG00323.hp1 HG00642.hp1 others(16): Show |
intron_variant | MODIFIER | c.160+345G>T | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 4/12 | chr19 | 35049861 | |||||||
| chr19:35049861 | GT | G | 171 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(168): Show |
203 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(200): Show |
intron_variant | MODIFIER | c.160+360delT | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr19 | 35049861 | ||||||
| chr19:35049866 | T | G | 1 | a0001c0001t0001g0223 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.160+350T>G | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 4/12 | chr19 | 35049866 | |||||||
| chr19:35049909 | C | T | 1 | a0001c0001t0002g0053 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.160+393C>T | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 4/12 | chr19 | 35049909 | |||||||
| chr19:35049978 | A | G | 253 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(250): Show |
294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.160+462A>G | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 4/12 | chr19 | 35049978 | |||||||
| chr19:35050090 | A | T | 54 | a0001c0001t0001g0011 a0001c0001t0001g0023 a0001c0001t0001g0054 others(51): Show |
57 | HG00099.hp1 HG00423.hp1 HG00621.hp1 others(54): Show |
intron_variant | MODIFIER | c.160+574A>T | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 4/12 | chr19 | 35050090 | |||||||
| chr19:35050200 | G | A | 26 | a0001c0001t0001g0075 a0001c0001t0001g0098 a0001c0001t0001g0171 others(23): Show |
29 | HG00140.hp1 HG00733.hp2 HG01074.hp2 others(26): Show |
intron_variant | MODIFIER | c.160+684G>A | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 4/12 | chr19 | 35050200 | |||||||
| chr19:35050338 | G | A | 7 | a0001c0001t0002g0126 a0001c0001t0002g0206 a0001c0001t0002g0229 others(4): Show |
7 | HG02647.hp1 HG02886.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.160+822G>A | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 4/12 | chr19 | 35050338 | |||||||
| chr19:35050344 | T | G | 279 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(276): Show |
325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.160+828T>G | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 4/12 | chr19 | 35050344 | |||||||
| chr19:35050351 | T | G | 1 | a0001c0001t0002g0263 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.160+835T>G | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 4/12 | chr19 | 35050351 | |||||||
| chr19:35050374 | G | A | 133 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(130): Show |
154 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.160+858G>A | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 4/12 | chr19 | 35050374 | |||||||
| chr19:35050426 | TA | T | 279 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(276): Show |
325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.160+912delA | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr19 | 35050426 | ||||||
| chr19:35050501 | C | A | 1 | a0001c0001t0001g0217 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.160+985C>A | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 4/12 | chr19 | 35050501 | |||||||
| chr19:35050542 | G | A | 1 | a0001c0001t0001g0063 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.160+1026G>A | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 4/12 | chr19 | 35050542 | |||||||
| chr19:35050635 | C | T | 6 | a0001c0001t0003g0004 a0001c0001t0003g0049 a0001c0001t0003g0258 others(3): Show |
9 | HG01884.hp1 HG02109.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.160+1119C>T | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 4/12 | chr19 | 35050635 | |||||||
| chr19:35050676 | T | C | 1 | a0001c0002t0002g0140 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.160+1160T>C | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 4/12 | chr19 | 35050676 | |||||||
| chr19:35050819 | A | G | 2 | a0001c0001t0002g0042 a0001c0001t0002g0046 |
2 | HG02257.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.160+1303A>G | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 4/12 | chr19 | 35050819 | |||||||
| chr19:35050910 | CT | C | 6 | a0001c0001t0003g0004 a0001c0001t0003g0049 a0001c0001t0003g0258 others(3): Show |
9 | HG01884.hp1 HG02109.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.160+1397delT | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr19 | 35050910 | ||||||
| chr19:35050913 | T | C | 1 | a0001c0001t0002g0053 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.160+1397T>C | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 4/12 | chr19 | 35050913 | |||||||
| chr19:35050914 | C | CT | 24 | a0001c0001t0001g0066 a0001c0001t0002g0043 a0001c0001t0002g0051 others(21): Show |
29 | HG00733.hp1 HG01070.hp2 HG01167.hp1 others(26): Show |
intron_variant | MODIFIER | c.160+1418dupT | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr19 | 35050914 | ||||||
| chr19:35050914 | C | T | 1 | a0001c0001t0002g0053 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.160+1398C>T | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 4/12 | chr19 | 35050914 | |||||||
| chr19:35050914 | CT | C | 188 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(185): Show |
223 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.160+1418delT | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr19 | 35050914 | ||||||
| chr19:35050914 | CTT | C | 6 | a0001c0001t0001g0069 a0001c0001t0001g0078 a0001c0001t0001g0117 others(3): Show |
6 | HG01255.hp2 HG01516.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.160+1417_160+1418d others(4): Show |
HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr19 | 35050914 | ||||||
| chr19:35050918 | T | C | 5 | a0001c0001t0002g0107 a0001c0001t0002g0129 a0001c0001t0002g0231 others(2): Show |
5 | HG01516.hp1 HG03486.hp1 HG03927.hp2 others(2): Show |
intron_variant | MODIFIER | c.160+1402T>C | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 4/12 | chr19 | 35050918 | |||||||
| chr19:35050940 | G | A | 1 | a0001c0001t0002g0272 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.160+1424G>A | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 4/12 | chr19 | 35050940 | |||||||
| chr19:35051003 | A | G | 1 | a0001c0001t0001g0080 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.160+1487A>G | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 4/12 | chr19 | 35051003 | |||||||
| chr19:35051148 | G | A | 3 | a0001c0001t0002g0107 a0001c0001t0002g0129 a0001c0001t0002g0280 |
3 | HG03927.hp2 HG04115.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.160+1632G>A | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 4/12 | chr19 | 35051148 | |||||||
| chr19:35051172 | G | A | 1 | a0001c0001t0001g0068 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.160+1656G>A | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 4/12 | chr19 | 35051172 | |||||||
| chr19:35051255 | C | T | 17 | a0001c0001t0002g0028 a0001c0001t0002g0030 a0001c0001t0002g0052 others(14): Show |
19 | HG00280.hp1 HG00323.hp1 HG00642.hp1 others(16): Show |
intron_variant | MODIFIER | c.160+1739C>T | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 4/12 | chr19 | 35051255 | |||||||
| chr19:35051356 | G | A | 2 | a0001c0001t0002g0194 a0001c0001t0002g0262 |
2 | HG01884.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.160+1840G>A | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 4/12 | chr19 | 35051356 | |||||||
| chr19:35051603 | G | A | 1 | a0001c0001t0002g0280 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.160+2087G>A | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 4/12 | chr19 | 35051603 | |||||||
| chr19:35051629 | G | A | 7 | a0001c0001t0002g0126 a0001c0001t0002g0206 a0001c0001t0002g0229 others(4): Show |
7 | HG02647.hp1 HG02886.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.160+2113G>A | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 4/12 | chr19 | 35051629 | |||||||
| chr19:35051646 | G | A | 1 | a0001c0001t0002g0124 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.160+2130G>A | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 4/12 | chr19 | 35051646 | |||||||
| chr19:35051684 | TA | T | 164 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(161): Show |
197 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(194): Show |
intron_variant | MODIFIER | c.160+2183delA | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr19 | 35051684 | ||||||
| chr19:35051902 | A | G | 7 | a0001c0001t0002g0126 a0001c0001t0002g0206 a0001c0001t0002g0229 others(4): Show |
7 | HG02647.hp1 HG02886.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.160+2386A>G | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 4/12 | chr19 | 35051902 | |||||||
| chr19:35051903 | A | G | 1 | a0001c0002t0002g0137 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.160+2387A>G | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 4/12 | chr19 | 35051903 | |||||||
| chr19:35051922 | G | A | 15 | a0001c0001t0002g0028 a0001c0001t0002g0030 a0001c0001t0002g0052 others(12): Show |
17 | HG00280.hp1 HG00323.hp1 HG00642.hp1 others(14): Show |
intron_variant | MODIFIER | c.160+2406G>A | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 4/12 | chr19 | 35051922 | |||||||
| chr19:35052281 | A | T | 1 | a0001c0001t0001g0202 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.160+2765A>T | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 4/12 | chr19 | 35052281 | |||||||
| chr19:35052344 | G | A | 17 | a0001c0001t0002g0053 a0001c0001t0002g0107 a0001c0001t0002g0126 others(14): Show |
20 | HG01884.hp1 HG02109.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.160+2828G>A | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 4/12 | chr19 | 35052344 | |||||||
| chr19:35052389 | G | A | 1 | a0001c0001t0002g0044 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.160+2873G>A | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 4/12 | chr19 | 35052389 | |||||||
| chr19:35052397 | G | A | 1 | a0001c0001t0002g0062 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.160+2881G>A | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 4/12 | chr19 | 35052397 | |||||||
| chr19:35052459 | C | T | 1 | a0001c0001t0001g0285 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.160+2943C>T | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 4/12 | chr19 | 35052459 | |||||||
| chr19:35052461 | C | T | 4 | a0001c0001t0002g0044 a0001c0001t0002g0231 a0001c0001t0002g0253 others(1): Show |
4 | HG03130.hp2 HG03195.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.160+2945C>T | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 4/12 | chr19 | 35052461 | |||||||
| chr19:35052534 | C | CA | 10 | a0001c0001t0001g0151 a0001c0001t0001g0219 a0001c0001t0002g0120 others(7): Show |
10 | HG01175.hp1 HG01496.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.160+3039dupA | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr19 | 35052534 | ||||||
| chr19:35052534 | C | CAAAAAA | 13 | a0001c0001t0002g0028 a0001c0001t0002g0030 a0001c0001t0002g0052 others(10): Show |
15 | HG00280.hp1 HG00323.hp1 HG01069.hp1 others(12): Show |
intron_variant | MODIFIER | c.160+3034_160+3039d others(8): Show |
HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr19 | 35052534 | ||||||
| chr19:35052534 | CA | C | 223 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(220): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.160+3039delA | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr19 | 35052534 | ||||||
| chr19:35052534 | CAA | C | 8 | a0001c0001t0001g0155 a0001c0001t0001g0188 a0001c0001t0002g0051 others(5): Show |
8 | HG01169.hp2 HG01257.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.160+3038_160+3039d others(4): Show |
HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr19 | 35052534 | ||||||
| chr19:35052663 | A | G | 7 | a0001c0001t0002g0053 a0001c0001t0003g0004 a0001c0001t0003g0049 others(4): Show |
10 | HG01884.hp1 HG02109.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.160+3147A>G | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 4/12 | chr19 | 35052663 | |||||||
| chr19:35052770 | T | G | 3 | a0001c0001t0002g0206 a0001c0001t0002g0229 a0001c0001t0002g0230 |
3 | HG02886.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.160+3254T>G | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 4/12 | chr19 | 35052770 | |||||||
| chr19:35052852 | G | A | 214 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(211): Show |
252 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(249): Show |
intron_variant | MODIFIER | c.160+3336G>A | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 4/12 | chr19 | 35052852 | |||||||
| chr19:35052909 | C | A | 52 | a0001c0001t0001g0011 a0001c0001t0001g0023 a0001c0001t0001g0055 others(49): Show |
55 | HG00099.hp1 HG00423.hp1 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.160+3393C>A | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 4/12 | chr19 | 35052909 | |||||||
| chr19:35052934 | C | A | 3 | a0001c0001t0002g0043 a0001c0001t0002g0120 a0001c0001t0002g0272 |
3 | HG02258.hp2 HG02818.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.160+3418C>A | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 4/12 | chr19 | 35052934 | |||||||
| chr19:35053272 | C | T | 1 | a0001c0001t0002g0168 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.160+3756C>T | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 4/12 | chr19 | 35053272 | |||||||
| chr19:35053399 | C | G | 1 | a0001c0001t0002g0048 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.160+3883C>G | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 4/12 | chr19 | 35053399 | |||||||
| chr19:35053430 | C | T | 1 | a0001c0001t0003g0049 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.160+3914C>T | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 4/12 | chr19 | 35053430 | |||||||
| chr19:35053606 | G | A | 1 | a0004c0008t0001g0205 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.160+4090G>A | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 4/12 | chr19 | 35053606 | |||||||
| chr19:35053648 | G | A | 5 | a0001c0001t0002g0083 a0001c0001t0002g0084 a0001c0001t0002g0094 others(2): Show |
5 | HG00741.hp1 HG02559.hp2 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.160+4132G>A | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 4/12 | chr19 | 35053648 | |||||||
| chr19:35054059 | G | A | 175 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(172): Show |
208 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(205): Show |
intron_variant | MODIFIER | c.160+4543G>A | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 4/12 | chr19 | 35054059 | |||||||
| chr19:35054162 | A | G | 1 | a0001c0001t0002g0248 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.160+4646A>G | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 4/12 | chr19 | 35054162 | |||||||
| chr19:35054205 | G | A | 16 | a0001c0001t0002g0028 a0001c0001t0002g0030 a0001c0001t0002g0052 others(13): Show |
18 | HG00280.hp1 HG00323.hp1 HG00642.hp1 others(15): Show |
intron_variant | MODIFIER | c.160+4689G>A | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 4/12 | chr19 | 35054205 | |||||||
| chr19:35054215 | T | C | 268 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(265): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.160+4699T>C | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 4/12 | chr19 | 35054215 | |||||||
| chr19:35054374 | T | C | 92 | a0001c0001t0001g0011 a0001c0001t0001g0023 a0001c0001t0001g0055 others(89): Show |
100 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.160+4858T>C | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 4/12 | chr19 | 35054374 | |||||||
| chr19:35054417 | C | CA | 77 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0024 others(74): Show |
86 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.160+4918dupA | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr19 | 35054417 | ||||||
| chr19:35054417 | C | CAA | 8 | a0001c0001t0001g0071 a0001c0001t0001g0128 a0001c0001t0001g0269 others(5): Show |
8 | HG00639.hp2 HG02293.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.160+4917_160+4918d others(4): Show |
HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr19 | 35054417 | ||||||
| chr19:35054417 | CA | C | 13 | a0001c0001t0001g0176 a0001c0001t0002g0126 a0001c0001t0002g0206 others(10): Show |
16 | HG01070.hp1 HG01884.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.160+4918delA | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr19 | 35054417 | ||||||
| chr19:35054481 | C | T | 23 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0002g0010 others(20): Show |
27 | HG00423.hp2 HG01106.hp2 HG02071.hp1 others(24): Show |
intron_variant | MODIFIER | c.160+4965C>T | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 4/12 | chr19 | 35054481 | |||||||
| chr19:35054674 | G | A | 4 | a0001c0001t0002g0092 a0001c0001t0002g0172 a0001c0001t0002g0173 others(1): Show |
4 | HG01106.hp2 HG03239.hp2 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.161-4999G>A | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 4/12 | chr19 | 35054674 | |||||||
| chr19:35054728 | C | T | 1 | a0001c0001t0002g0121 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.161-4945C>T | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 4/12 | chr19 | 35054728 | |||||||
| chr19:35054838 | G | T | 3 | a0001c0001t0002g0107 a0001c0001t0002g0129 a0001c0001t0002g0280 |
3 | HG03927.hp2 HG04115.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.161-4835G>T | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 4/12 | chr19 | 35054838 | |||||||
| chr19:35054902 | C | T | 1 | a0001c0001t0001g0284 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.161-4771C>T | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 4/12 | chr19 | 35054902 | |||||||
| chr19:35054990 | A | G | 1 | a0001c0001t0002g0263 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.161-4683A>G | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 4/12 | chr19 | 35054990 | |||||||
| chr19:35055028 | A | G | 5 | a0001c0001t0001g0277 a0001c0001t0001g0312 a0001c0001t0001g0314 others(2): Show |
5 | HG02080.hp2 NA18982.hp1 NA19009.hp2 others(2): Show |
intron_variant | MODIFIER | c.161-4645A>G | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 4/12 | chr19 | 35055028 | |||||||
| chr19:35055239 | A | G | 19 | a0001c0001t0002g0053 a0001c0001t0002g0107 a0001c0001t0002g0126 others(16): Show |
22 | HG01884.hp1 HG02109.hp2 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.161-4434A>G | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 4/12 | chr19 | 35055239 | |||||||
| chr19:35055303 | G | A | 6 | a0001c0001t0003g0004 a0001c0001t0003g0049 a0001c0001t0003g0258 others(3): Show |
9 | HG01884.hp1 HG02109.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.161-4370G>A | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 4/12 | chr19 | 35055303 | |||||||
| chr19:35055312 | G | A | 3 | a0001c0001t0001g0204 a0001c0001t0001g0243 a0001c0001t0002g0053 |
3 | HG00673.hp2 HG02155.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.161-4361G>A | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 4/12 | chr19 | 35055312 | |||||||
| chr19:35055393 | T | C | 1 | a0001c0001t0001g0139 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.161-4280T>C | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 4/12 | chr19 | 35055393 | |||||||
| chr19:35055403 | G | GA | 285 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(282): Show |
331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.161-4260dupA | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr19 | 35055403 | ||||||
| chr19:35055440 | C | G | 3 | a0001c0001t0002g0107 a0001c0001t0002g0129 a0001c0001t0002g0280 |
3 | HG03927.hp2 HG04115.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.161-4233C>G | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 4/12 | chr19 | 35055440 | |||||||
| chr19:35055483 | G | A | 13 | a0001c0001t0002g0040 a0001c0001t0002g0041 a0001c0001t0002g0042 others(10): Show |
13 | HG01109.hp1 HG02257.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.161-4190G>A | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 4/12 | chr19 | 35055483 | |||||||
| chr19:35055687 | A | G | 18 | a0001c0001t0002g0028 a0001c0001t0002g0030 a0001c0001t0002g0052 others(15): Show |
20 | HG00280.hp1 HG00323.hp1 HG00642.hp1 others(17): Show |
intron_variant | MODIFIER | c.161-3986A>G | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 4/12 | chr19 | 35055687 | |||||||
| chr19:35055730 | A | G | 1 | a0001c0001t0001g0211 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.161-3943A>G | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 4/12 | chr19 | 35055730 | |||||||
| chr19:35055800 | G | T | 1 | a0001c0001t0001g0074 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.161-3873G>T | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 4/12 | chr19 | 35055800 | |||||||
| chr19:35055866 | T | C | 1 | a0001c0001t0001g0183 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.161-3807T>C | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 4/12 | chr19 | 35055866 | |||||||
| chr19:35055915 | C | T | 1 | a0001c0001t0001g0101 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.161-3758C>T | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 4/12 | chr19 | 35055915 | |||||||
| chr19:35055921 | T | A | 1 | a0001c0001t0001g0308 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.161-3752T>A | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 4/12 | chr19 | 35055921 | |||||||
| chr19:35055922 | G | T | 2 | a0001c0001t0001g0035 a0001c0001t0001g0247 |
3 | NA19011.hp2 NA19065.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.161-3751G>T | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 4/12 | chr19 | 35055922 | |||||||
| chr19:35056137 | G | T | 16 | a0001c0001t0002g0028 a0001c0001t0002g0030 a0001c0001t0002g0052 others(13): Show |
18 | HG00280.hp1 HG00323.hp1 HG00642.hp1 others(15): Show |
intron_variant | MODIFIER | c.161-3536G>T | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 4/12 | chr19 | 35056137 | |||||||
| chr19:35056147 | T | C | 286 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(283): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.161-3526T>C | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 4/12 | chr19 | 35056147 | |||||||
| chr19:35056214 | T | C | 270 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(267): Show |
311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.161-3459T>C | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 4/12 | chr19 | 35056214 | |||||||
| chr19:35056215 | G | A | 57 | a0001c0001t0001g0011 a0001c0001t0001g0023 a0001c0001t0001g0055 others(54): Show |
60 | HG00099.hp1 HG00423.hp1 HG00621.hp1 others(57): Show |
intron_variant | MODIFIER | c.161-3458G>A | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 4/12 | chr19 | 35056215 | |||||||
| chr19:35056353 | G | T | 1 | a0001c0001t0002g0262 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.161-3320G>T | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 4/12 | chr19 | 35056353 | |||||||
| chr19:35056674 | A | G | 1 | a0001c0001t0002g0168 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.161-2999A>G | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 4/12 | chr19 | 35056674 | |||||||
| chr19:35056717 | G | A | 2 | a0001c0001t0002g0194 a0001c0001t0002g0262 |
2 | HG01884.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.161-2956G>A | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 4/12 | chr19 | 35056717 | |||||||
| chr19:35056731 | C | T | 1 | a0001c0001t0002g0168 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.161-2942C>T | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 4/12 | chr19 | 35056731 | |||||||
| chr19:35056790 | G | A | 1 | a0001c0001t0002g0131 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.161-2883G>A | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 4/12 | chr19 | 35056790 | |||||||
| chr19:35056892 | TTTTC | T | 35 | a0001c0001t0001g0011 a0001c0001t0001g0023 a0001c0001t0001g0055 others(32): Show |
38 | HG00099.hp1 HG00423.hp1 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.161-2768_161-2765d others(6): Show |
HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr19 | 35056892 | ||||||
| chr19:35057017 | G | A | 1 | a0001c0001t0001g0184 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.161-2656G>A | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 4/12 | chr19 | 35057017 | |||||||
| chr19:35057080 | C | G | 55 | a0001c0001t0001g0011 a0001c0001t0001g0023 a0001c0001t0001g0055 others(52): Show |
58 | HG00099.hp1 HG00423.hp1 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.161-2593C>G | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 4/12 | chr19 | 35057080 | |||||||
| chr19:35057194 | A | C | 16 | a0001c0001t0002g0028 a0001c0001t0002g0030 a0001c0001t0002g0052 others(13): Show |
18 | HG00280.hp1 HG00323.hp1 HG00642.hp1 others(15): Show |
intron_variant | MODIFIER | c.161-2479A>C | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 4/12 | chr19 | 35057194 | |||||||
| chr19:35057235 | G | A | 16 | a0001c0001t0002g0028 a0001c0001t0002g0030 a0001c0001t0002g0052 others(13): Show |
18 | HG00280.hp1 HG00323.hp1 HG00642.hp1 others(15): Show |
intron_variant | MODIFIER | c.161-2438G>A | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 4/12 | chr19 | 35057235 | |||||||
| chr19:35057253 | C | T | 1 | a0001c0001t0001g0297 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.161-2420C>T | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 4/12 | chr19 | 35057253 | |||||||
| chr19:35057254 | G | A | 2 | a0001c0001t0002g0194 a0001c0001t0002g0262 |
2 | HG01884.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.161-2419G>A | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 4/12 | chr19 | 35057254 | |||||||
| chr19:35057261 | C | CACGGTTT others(1): Show |
3 | a0001c0001t0002g0107 a0001c0001t0002g0129 a0001c0001t0002g0280 |
3 | HG03927.hp2 HG04115.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.161-2412_161-2411i others(10): Show |
HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 4/12 | chr19 | 35057261 | |||||||
| chr19:35057276 | A | G | 3 | a0001c0001t0002g0107 a0001c0001t0002g0129 a0001c0001t0002g0280 |
3 | HG03927.hp2 HG04115.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.161-2397A>G | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 4/12 | chr19 | 35057276 | |||||||
| chr19:35057295 | A | C | 3 | a0001c0001t0001g0290 a0001c0001t0001g0291 a0001c0001t0001g0293 |
3 | HG01361.hp1 HG01433.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.161-2378A>C | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 4/12 | chr19 | 35057295 | |||||||
| chr19:35057425 | C | CA | 37 | a0001c0001t0001g0080 a0001c0001t0002g0028 a0001c0001t0002g0030 others(34): Show |
42 | HG00280.hp1 HG00323.hp1 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.161-2233dupA | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr19 | 35057425 | ||||||
| chr19:35057589 | G | T | 1 | a0001c0001t0003g0259 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.161-2084G>T | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 4/12 | chr19 | 35057589 | |||||||
| chr19:35057751 | G | C | 1 | a0001c0001t0002g0043 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.161-1922G>C | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 4/12 | chr19 | 35057751 | |||||||
| chr19:35057790 | C | T | 1 | a0001c0001t0001g0323 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.161-1883C>T | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 4/12 | chr19 | 35057790 | |||||||
| chr19:35057980 | A | G | 1 | a0001c0001t0001g0057 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.161-1693A>G | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 4/12 | chr19 | 35057980 | |||||||
| chr19:35057987 | C | T | 1 | a0001c0002t0002g0130 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.161-1686C>T | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 4/12 | chr19 | 35057987 | |||||||
| chr19:35058013 | C | T | 18 | a0001c0001t0002g0053 a0001c0001t0002g0107 a0001c0001t0002g0126 others(15): Show |
21 | HG01884.hp1 HG02109.hp2 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.161-1660C>T | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 4/12 | chr19 | 35058013 | |||||||
| chr19:35058051 | GC | G | 14 | a0001c0001t0002g0053 a0001c0001t0002g0126 a0001c0001t0002g0206 others(11): Show |
17 | HG01884.hp1 HG02109.hp2 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.161-1621delC | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 4/12 | chr19 | 35058051 | |||||||
| chr19:35058077 | C | T | 1 | a0001c0001t0001g0184 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.161-1596C>T | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 4/12 | chr19 | 35058077 | |||||||
| chr19:35058078 | G | A | 1 | a0001c0001t0001g0080 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.161-1595G>A | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 4/12 | chr19 | 35058078 | |||||||
| chr19:35058082 | G | A | 57 | a0001c0001t0001g0011 a0001c0001t0001g0023 a0001c0001t0001g0055 others(54): Show |
60 | HG00099.hp1 HG00423.hp1 HG00621.hp1 others(57): Show |
intron_variant | MODIFIER | c.161-1591G>A | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 4/12 | chr19 | 35058082 | |||||||
| chr19:35058189 | T | C | 55 | a0001c0001t0001g0011 a0001c0001t0001g0023 a0001c0001t0001g0055 others(52): Show |
58 | HG00099.hp1 HG00423.hp1 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.161-1484T>C | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 4/12 | chr19 | 35058189 | |||||||
| chr19:35058218 | C | T | 13 | a0001c0002t0002g0001 a0001c0002t0002g0022 a0001c0002t0002g0059 others(10): Show |
18 | HG00642.hp2 HG00733.hp1 HG01070.hp2 others(15): Show |
intron_variant | MODIFIER | c.161-1455C>T | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 4/12 | chr19 | 35058218 | |||||||
| chr19:35058242 | C | T | 1 | a0001c0001t0002g0043 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.161-1431C>T | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 4/12 | chr19 | 35058242 | |||||||
| chr19:35058258 | C | A | 2 | a0001c0001t0001g0283 a0001c0001t0001g0284 |
2 | HG02647.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.161-1415C>A | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 4/12 | chr19 | 35058258 | |||||||
| chr19:35058305 | G | A | 1 | a0001c0001t0002g0043 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.161-1368G>A | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 4/12 | chr19 | 35058305 | |||||||
| chr19:35058375 | T | A | 16 | a0001c0001t0002g0028 a0001c0001t0002g0030 a0001c0001t0002g0052 others(13): Show |
18 | HG00280.hp1 HG00323.hp1 HG00642.hp1 others(15): Show |
intron_variant | MODIFIER | c.161-1298T>A | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 4/12 | chr19 | 35058375 | |||||||
| chr19:35058378 | T | C | 1 | a0001c0001t0002g0168 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.161-1295T>C | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 4/12 | chr19 | 35058378 | |||||||
| chr19:35058382 | C | G | 1 | a0001c0001t0002g0168 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.161-1291C>G | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 4/12 | chr19 | 35058382 | |||||||
| chr19:35058497 | TATA | T | 91 | a0001c0001t0001g0011 a0001c0001t0001g0023 a0001c0001t0001g0055 others(88): Show |
99 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.161-1163_161-1161d others(5): Show |
HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr19 | 35058497 | ||||||
| chr19:35058556 | T | C | 18 | a0001c0001t0002g0053 a0001c0001t0002g0107 a0001c0001t0002g0126 others(15): Show |
21 | HG01884.hp1 HG02109.hp2 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.161-1117T>C | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 4/12 | chr19 | 35058556 | |||||||
| chr19:35058608 | TTAA | T | 3 | a0001c0001t0002g0107 a0001c0001t0002g0129 a0001c0001t0002g0280 |
3 | HG03927.hp2 HG04115.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.161-1062_161-1060d others(5): Show |
HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr19 | 35058608 | ||||||
| chr19:35058656 | A | C | 55 | a0001c0001t0001g0011 a0001c0001t0001g0023 a0001c0001t0001g0055 others(52): Show |
58 | HG00099.hp1 HG00423.hp1 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.161-1017A>C | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 4/12 | chr19 | 35058656 | |||||||
| chr19:35059282 | C | G | 1 | a0001c0001t0001g0056 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.161-391C>G | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 4/12 | chr19 | 35059282 | |||||||
| chr19:35059295 | T | TACAAA | 6 | a0001c0001t0003g0004 a0001c0001t0003g0049 a0001c0001t0003g0258 others(3): Show |
9 | HG01884.hp1 HG02109.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.161-357_161-353dup others(5): Show |
HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr19 | 35059295 | ||||||
| chr19:35059295 | T | TACAAAAC others(3): Show |
1 | a0001c0001t0002g0053 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.161-362_161-353dup others(10): Show |
HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr19 | 35059295 | ||||||
| chr19:35059302 | C | T | 175 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(172): Show |
208 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(205): Show |
intron_variant | MODIFIER | c.161-371C>T | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 4/12 | chr19 | 35059302 | |||||||
| chr19:35059325 | C | A | 1 | a0001c0001t0002g0262 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.161-348C>A | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 4/12 | chr19 | 35059325 | |||||||
| chr19:35059337 | T | C | 268 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(265): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.161-336T>C | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 4/12 | chr19 | 35059337 | |||||||
| chr19:35059354 | C | T | 1 | a0001c0001t0002g0168 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.161-319C>T | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 4/12 | chr19 | 35059354 | |||||||
| chr19:35059574 | A | G | 1 | a0001c0001t0001g0296 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.161-99A>G | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 4/12 | chr19 | 35059574 | |||||||
| chr19:35060321 | G | GC | 54 | a0001c0001t0001g0011 a0001c0001t0001g0023 a0001c0001t0001g0055 others(51): Show |
57 | HG00099.hp1 HG00423.hp1 HG00621.hp1 others(54): Show |
intron_variant | MODIFIER | c.455-21dupC | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 35060321 | ||||||
| chr19:35060336 | T | C | 12 | a0001c0001t0002g0107 a0001c0001t0002g0126 a0001c0001t0002g0129 others(9): Show |
12 | HG02622.hp1 HG02647.hp1 HG02886.hp2 others(9): Show |
intron_variant | MODIFIER | c.455-11T>C | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 7/12 | chr19 | 35060336 | |||||||
| chr19:35060523 | C | T | 3 | a0001c0001t0002g0107 a0001c0001t0002g0129 a0001c0001t0002g0280 |
3 | HG03927.hp2 HG04115.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.620+11C>T | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 8/12 | chr19 | 35060523 | |||||||
| chr19:35060524 | C | A | 13 | a0001c0002t0002g0001 a0001c0002t0002g0022 a0001c0002t0002g0059 others(10): Show |
18 | HG00642.hp2 HG00733.hp1 HG01070.hp2 others(15): Show |
intron_variant | MODIFIER | c.620+12C>A | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 8/12 | chr19 | 35060524 | |||||||
| chr19:35060828 | G | A | 19 | a0001c0001t0002g0053 a0001c0001t0002g0107 a0001c0001t0002g0126 others(16): Show |
22 | HG01884.hp1 HG02109.hp2 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.811+11G>A | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 9/12 | chr19 | 35060828 | |||||||
| chr19:35060838 | A | T | 19 | a0001c0001t0002g0053 a0001c0001t0002g0107 a0001c0001t0002g0126 others(16): Show |
22 | HG01884.hp1 HG02109.hp2 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.811+21A>T | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 9/12 | chr19 | 35060838 | |||||||
| chr19:35060934 | A | G | 15 | a0001c0001t0002g0028 a0001c0001t0002g0030 a0001c0001t0002g0052 others(12): Show |
17 | HG00280.hp1 HG00323.hp1 HG00642.hp1 others(14): Show |
intron_variant | MODIFIER | c.811+117A>G | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 9/12 | chr19 | 35060934 | |||||||
| chr19:35060951 | C | T | 1 | a0001c0001t0001g0036 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.811+134C>T | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 9/12 | chr19 | 35060951 | |||||||
| chr19:35061114 | C | T | 1 | a0001c0001t0002g0129 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.811+297C>T | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 9/12 | chr19 | 35061114 | |||||||
| chr19:35061119 | A | G | 3 | a0001c0001t0001g0211 a0001c0001t0001g0216 a0001c0001t0001g0251 |
3 | HG00609.hp1 NA18966.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.811+302A>G | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 9/12 | chr19 | 35061119 | |||||||
| chr19:35061175 | C | G | 265 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(262): Show |
308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.811+358C>G | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 9/12 | chr19 | 35061175 | |||||||
| chr19:35061299 | C | CAGCCTGG others(189): Show |
1 | a0001c0001t0002g0124 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.811+637_811+638ins others(196): Show |
HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr19 | 35061299 | ||||||
| chr19:35061299 | CAGCCTGG others(42): Show |
C | 7 | a0001c0001t0001g0111 a0001c0001t0003g0004 a0001c0001t0003g0049 others(4): Show |
10 | HG01884.hp1 HG02109.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.811+589_811+637del others(49): Show |
HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr19 | 35061299 | ||||||
| chr19:35061542 | C | T | 1 | a0001c0001t0001g0222 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.811+725C>T | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 9/12 | chr19 | 35061542 | |||||||
| chr19:35061585 | C | T | 1 | a0001c0001t0002g0154 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.811+768C>T | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 9/12 | chr19 | 35061585 | |||||||
| chr19:35061674 | A | T | 1 | a0001c0001t0002g0044 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.811+857A>T | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 9/12 | chr19 | 35061674 | |||||||
| chr19:35061922 | G | T | 15 | a0001c0001t0002g0028 a0001c0001t0002g0030 a0001c0001t0002g0052 others(12): Show |
17 | HG00280.hp1 HG00323.hp1 HG00642.hp1 others(14): Show |
intron_variant | MODIFIER | c.811+1105G>T | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 9/12 | chr19 | 35061922 | |||||||
| chr19:35062059 | TA | T | 268 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(265): Show |
311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.811+1249delA | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr19 | 35062059 | ||||||
| chr19:35062088 | G | T | 7 | a0001c0001t0002g0053 a0001c0001t0003g0004 a0001c0001t0003g0049 others(4): Show |
10 | HG01884.hp1 HG02109.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.811+1271G>T | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 9/12 | chr19 | 35062088 | |||||||
| chr19:35062368 | G | A | 4 | a0001c0001t0002g0126 a0001c0001t0002g0255 a0001c0001t0002g0257 others(1): Show |
4 | HG02647.hp1 HG02965.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.811+1551G>A | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 9/12 | chr19 | 35062368 | |||||||
| chr19:35062372 | A | C | 4 | a0001c0003t0002g0158 a0001c0003t0002g0164 a0001c0003t0002g0165 others(1): Show |
4 | HG03225.hp1 HG03453.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.811+1555A>C | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 9/12 | chr19 | 35062372 | |||||||
| chr19:35062402 | T | A | 3 | a0001c0001t0001g0111 a0001c0001t0001g0148 a0001c0001t0001g0183 |
3 | HG02155.hp1 HG02523.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.811+1585T>A | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 9/12 | chr19 | 35062402 | |||||||
| chr19:35062418 | T | TA | 268 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(265): Show |
311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.811+1606dupA | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr19 | 35062418 | ||||||
| chr19:35062437 | C | T | 285 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(282): Show |
331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.811+1620C>T | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 9/12 | chr19 | 35062437 | |||||||
| chr19:35062471 | A | G | 8 | a0001c0001t0002g0126 a0001c0001t0002g0206 a0001c0001t0002g0229 others(5): Show |
8 | HG02647.hp1 HG02886.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.811+1654A>G | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 9/12 | chr19 | 35062471 | |||||||
| chr19:35062482 | T | G | 2 | a0001c0001t0002g0229 a0001c0001t0002g0230 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.811+1665T>G | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 9/12 | chr19 | 35062482 | |||||||
| chr19:35062545 | A | G | 268 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(265): Show |
311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.811+1728A>G | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 9/12 | chr19 | 35062545 | |||||||
| chr19:35062684 | A | T | 268 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(265): Show |
311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.811+1867A>T | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 9/12 | chr19 | 35062684 | |||||||
| chr19:35062693 | G | A | 268 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(265): Show |
311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.811+1876G>A | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 9/12 | chr19 | 35062693 | |||||||
| chr19:35062752 | G | A | 17 | a0001c0001t0002g0053 a0001c0001t0002g0107 a0001c0001t0002g0126 others(14): Show |
20 | HG01884.hp1 HG02109.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.811+1935G>A | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 9/12 | chr19 | 35062752 | |||||||
| chr19:35062753 | C | T | 2 | a0001c0001t0001g0099 a0001c0001t0001g0215 |
2 | NA18943.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.811+1936C>T | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 9/12 | chr19 | 35062753 | |||||||
| chr19:35062776 | G | A | 14 | a0001c0001t0002g0028 a0001c0001t0002g0030 a0001c0001t0002g0052 others(11): Show |
16 | HG00280.hp1 HG00323.hp1 HG00642.hp1 others(13): Show |
intron_variant | MODIFIER | c.811+1959G>A | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 9/12 | chr19 | 35062776 | |||||||
| chr19:35062780 | C | T | 3 | a0001c0001t0002g0107 a0001c0001t0002g0129 a0001c0001t0002g0280 |
3 | HG03927.hp2 HG04115.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.811+1963C>T | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 9/12 | chr19 | 35062780 | |||||||
| chr19:35062852 | C | T | 268 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(265): Show |
311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.811+2035C>T | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 9/12 | chr19 | 35062852 | |||||||
| chr19:35062860 | T | G | 268 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(265): Show |
311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.811+2043T>G | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 9/12 | chr19 | 35062860 | |||||||
| chr19:35062896 | AATAACGG others(2): Show |
A | 268 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(265): Show |
311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.811+2084_811+2092d others(11): Show |
HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr19 | 35062896 | ||||||
| chr19:35062926 | G | C | 268 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(265): Show |
311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.811+2109G>C | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 9/12 | chr19 | 35062926 | |||||||
| chr19:35063068 | C | T | 266 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(263): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.812-2182C>T | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 9/12 | chr19 | 35063068 | |||||||
| chr19:35063115 | A | C | 15 | a0001c0001t0002g0028 a0001c0001t0002g0030 a0001c0001t0002g0052 others(12): Show |
17 | HG00280.hp1 HG00323.hp1 HG00642.hp1 others(14): Show |
intron_variant | MODIFIER | c.812-2135A>C | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 9/12 | chr19 | 35063115 | |||||||
| chr19:35063266 | G | A | 1 | a0001c0001t0001g0285 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.812-1984G>A | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 9/12 | chr19 | 35063266 | |||||||
| chr19:35063270 | C | T | 7 | a0001c0001t0002g0053 a0001c0001t0003g0004 a0001c0001t0003g0049 others(4): Show |
10 | HG01884.hp1 HG02109.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.812-1980C>T | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 9/12 | chr19 | 35063270 | |||||||
| chr19:35063288 | C | T | 1 | a0001c0001t0002g0168 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.812-1962C>T | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 9/12 | chr19 | 35063288 | |||||||
| chr19:35063297 | G | T | 1 | a0001c0001t0002g0040 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.812-1953G>T | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 9/12 | chr19 | 35063297 | |||||||
| chr19:35063327 | G | C | 2 | a0001c0001t0001g0019 a0001c0001t0001g0102 |
3 | NA18940.hp2 NA18970.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.812-1923G>C | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 9/12 | chr19 | 35063327 | |||||||
| chr19:35063480 | G | A | 266 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(263): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.812-1770G>A | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 9/12 | chr19 | 35063480 | |||||||
| chr19:35063499 | G | A | 266 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(263): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.812-1751G>A | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 9/12 | chr19 | 35063499 | |||||||
| chr19:35063575 | G | A | 17 | a0001c0001t0002g0043 a0001c0001t0002g0120 a0001c0001t0002g0145 others(14): Show |
22 | HG00642.hp2 HG00733.hp1 HG01070.hp2 others(19): Show |
intron_variant | MODIFIER | c.812-1675G>A | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 9/12 | chr19 | 35063575 | |||||||
| chr19:35063847 | G | A | 194 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(191): Show |
232 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(229): Show |
intron_variant | MODIFIER | c.812-1403G>A | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 9/12 | chr19 | 35063847 | |||||||
| chr19:35063863 | C | T | 266 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(263): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.812-1387C>T | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 9/12 | chr19 | 35063863 | |||||||
| chr19:35063903 | T | C | 1 | a0001c0001t0001g0085 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.812-1347T>C | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 9/12 | chr19 | 35063903 | |||||||
| chr19:35063942 | G | C | 7 | a0001c0001t0002g0053 a0001c0001t0003g0004 a0001c0001t0003g0049 others(4): Show |
10 | HG01884.hp1 HG02109.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.812-1308G>C | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 9/12 | chr19 | 35063942 | |||||||
| chr19:35064136 | G | A | 1 | a0001c0001t0002g0121 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.812-1114G>A | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 9/12 | chr19 | 35064136 | |||||||
| chr19:35064149 | TCAGCAGG | T | 266 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(263): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.812-1084_812-1078d others(9): Show |
HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr19 | 35064149 | ||||||
| chr19:35064286 | T | C | 266 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(263): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.812-964T>C | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 9/12 | chr19 | 35064286 | |||||||
| chr19:35064318 | G | C | 2 | a0001c0001t0002g0052 a0001c0001t0002g0324 |
2 | HG02615.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.812-932G>C | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 9/12 | chr19 | 35064318 | |||||||
| chr19:35064318 | G | GTCTC | 50 | a0001c0001t0001g0011 a0001c0001t0001g0023 a0001c0001t0001g0055 others(47): Show |
53 | HG00099.hp1 HG00423.hp1 HG00621.hp1 others(50): Show |
intron_variant | MODIFIER | c.812-914_812-911dup others(4): Show |
HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr19 | 35064318 | ||||||
| chr19:35064318 | G | GTCTCTCT others(1): Show |
3 | a0001c0001t0002g0051 a0001c0001t0002g0263 a0001c0001t0002g0265 |
3 | HG03471.hp1 HG03516.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.812-918_812-911dup others(8): Show |
HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr19 | 35064318 | ||||||
| chr19:35064318 | GTC | G | 197 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(194): Show |
238 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(235): Show |
intron_variant | MODIFIER | c.812-912_812-911del others(2): Show |
HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr19 | 35064318 | ||||||
| chr19:35064340 | T | C | 2 | a0001c0001t0001g0298 a0001c0001t0001g0311 |
2 | NA18992.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.812-910T>C | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 9/12 | chr19 | 35064340 | |||||||
| chr19:35064345 | C | T | 2 | a0001c0001t0001g0298 a0001c0001t0001g0311 |
2 | NA18992.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.812-905C>T | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 9/12 | chr19 | 35064345 | |||||||
| chr19:35064346 | T | C | 2 | a0001c0001t0001g0298 a0001c0001t0001g0311 |
2 | NA18992.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.812-904T>C | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 9/12 | chr19 | 35064346 | |||||||
| chr19:35064347 | C | T | 2 | a0001c0001t0001g0298 a0001c0001t0001g0311 |
2 | NA18992.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.812-903C>T | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 9/12 | chr19 | 35064347 | |||||||
| chr19:35064681 | G | A | 193 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(190): Show |
231 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(228): Show |
intron_variant | MODIFIER | c.812-569G>A | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 9/12 | chr19 | 35064681 | |||||||
| chr19:35064779 | C | T | 58 | a0001c0001t0001g0011 a0001c0001t0001g0023 a0001c0001t0001g0055 others(55): Show |
61 | HG00099.hp1 HG00423.hp1 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.812-471C>T | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 9/12 | chr19 | 35064779 | |||||||
| chr19:35064808 | G | A | 1 | a0001c0001t0002g0192 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.812-442G>A | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 9/12 | chr19 | 35064808 | |||||||
| chr19:35064818 | TTTTG | T | 193 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(190): Show |
231 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(228): Show |
intron_variant | MODIFIER | c.812-416_812-413del others(4): Show |
HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr19 | 35064818 | ||||||
| chr19:35065023 | C | T | 193 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(190): Show |
231 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(228): Show |
intron_variant | MODIFIER | c.812-227C>T | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 9/12 | chr19 | 35065023 | |||||||
| chr19:35065092 | G | T | 193 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(190): Show |
231 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(228): Show |
intron_variant | MODIFIER | c.812-158G>T | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 9/12 | chr19 | 35065092 | |||||||
| chr19:35065129 | GT | G | 7 | a0001c0001t0002g0053 a0001c0001t0003g0004 a0001c0001t0003g0049 others(4): Show |
10 | HG01884.hp1 HG02109.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.812-111delT | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr19 | 35065129 | ||||||
| chr19:35065219 | G | A | 194 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(191): Show |
232 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(229): Show |
intron_variant | MODIFIER | c.812-31G>A | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 9/12 | chr19 | 35065219 | |||||||
| chr19:35065377 | G | A | 189 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(186): Show |
227 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(224): Show |
intron_variant | MODIFIER | c.907+32G>A | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 10/12 | chr19 | 35065377 | |||||||
| chr19:35065396 | A | G | 272 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(269): Show |
318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.907+51A>G | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 10/12 | chr19 | 35065396 | |||||||
| chr19:35065425 | GATGAGTC others(6): Show |
G | 1 | a0001c0001t0001g0260 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.907+86_908-96delTC others(11): Show |
HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr19 | 35065425 | ||||||
| chr19:35065453 | C | T | 189 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(186): Show |
227 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(224): Show |
intron_variant | MODIFIER | c.908-86C>T | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 10/12 | chr19 | 35065453 | |||||||
| chr19:35065736 | T | C | 230 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(227): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.1050+55T>C | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 11/12 | chr19 | 35065736 | |||||||
| chr19:35065755 | A | G | 273 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(270): Show |
319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
intron_variant | MODIFIER | c.1050+74A>G | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 11/12 | chr19 | 35065755 | |||||||
| chr19:35065761 | C | T | 6 | a0001c0001t0003g0004 a0001c0001t0003g0049 a0001c0001t0003g0258 others(3): Show |
9 | HG01884.hp1 HG02109.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.1050+80C>T | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 11/12 | chr19 | 35065761 | |||||||
| chr19:35065811 | GT | G | 229 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(226): Show |
270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.1051-56delT | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 11/12 | chr19 | 35065811 | |||||||
| chr19:35065825 | C | T | 230 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(227): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.1051-43C>T | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 11/12 | chr19 | 35065825 | |||||||
| chr19:35065840 | T | C | 273 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(270): Show |
319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
intron_variant | MODIFIER | c.1051-28T>C | HPN | ENSG00000105707.15 | transcript | ENST00000672452.2 | protein_coding | 11/12 | chr19 | 35065840 |