Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 83695 |
| ensemblid | ENSG00000171792.11 |
| hgncid | 28206 |
| symbol | RHNO1 |
| name | RAD9-HUS1-RAD1 interacting nuclear orphan 1 |
| refseq_nuc | NM_001252499.3 |
| refseq_prot | NP_001239428.1 |
| ensembl_nuc | ENST00000489288.7 |
| ensembl_prot | ENSP00000438590.1 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 2877223 |
| end | 2889524 |
| strand | + |
| ver | v1.2 |
| region | chr12:2877223-2889524 |
| region5000 | chr12:2872223-2894524 |
| regionname0 | RHNO1_chr12_2877223_2889524 |
| regionname5000 | RHNO1_chr12_2872223_2894524 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 238 | 423 | 93 | 76 | 198 | 14 | 40 | 156 | RHNO1_chr12_2872223_2894524 | RHNO1 | MPPRK others(233): Show |
chr12 | 2872223 | 2894524 |
| a0002 | 0/0 | 238 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | MPPRK others(233): Show |
chr12 | 2872223 | 2894524 |
| a0003 | 0/0 | 238 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | MPPRK others(233): Show |
chr12 | 2872223 | 2894524 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 714 | 252 | 60 | 42 | 122 | 3 | 24 | RHNO1_chr12_2872223_2894524 | RHNO1 | ATGCC others(709): Show |
chr12 | 2872223 | 2894524 | ||
| a0001c0002 | 1/0 | 714 | 169 | 33 | 33 | 75 | 11 | 16 | RHNO1_chr12_2872223_2894524 | RHNO1 | ATGCC others(709): Show |
chr12 | 2872223 | 2894524 | ||
| a0001c0004 | 0/0 | 714 | 1 | 0 | 1 | 0 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | ATGCC others(709): Show |
chr12 | 2872223 | 2894524 | ||
| a0001c0006 | 0/0 | 714 | 1 | 0 | 0 | 1 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | ATGCC others(709): Show |
chr12 | 2872223 | 2894524 | ||
| a0002c0003 | 0/0 | 714 | 2 | 0 | 0 | 0 | 0 | 2 | RHNO1_chr12_2872223_2894524 | RHNO1 | ATGCC others(709): Show |
chr12 | 2872223 | 2894524 | ||
| a0003c0005 | 0/0 | 714 | 1 | 1 | 0 | 0 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | ATGCC others(709): Show |
chr12 | 2872223 | 2894524 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 1926 | 162 | 24 | 31 | 86 | 3 | 17 | RHNO1_chr12_2872223_2894524 | RHNO1 | ATTCC others(1921): Show |
chr12 | 2872223 | 2894524 |
| a0001c0001t0002 | 0/0 | 1926 | 62 | 18 | 9 | 29 | 0 | 6 | RHNO1_chr12_2872223_2894524 | RHNO1 | ATTCC others(1921): Show |
chr12 | 2872223 | 2894524 |
| a0001c0001t0003 | 0/0 | 1926 | 17 | 16 | 1 | 0 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | ATTCC others(1921): Show |
chr12 | 2872223 | 2894524 |
| a0001c0001t0008 | 0/0 | 1926 | 2 | 0 | 0 | 2 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | ATTCC others(1921): Show |
chr12 | 2872223 | 2894524 |
| a0001c0001t0010 | 0/0 | 1926 | 1 | 1 | 0 | 0 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | ATTCC others(1921): Show |
chr12 | 2872223 | 2894524 |
| a0001c0001t0011 | 0/0 | 1926 | 1 | 0 | 1 | 0 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | ATTCC others(1921): Show |
chr12 | 2872223 | 2894524 |
| a0001c0001t0012 | 0/0 | 1926 | 1 | 0 | 0 | 1 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | ATTCC others(1921): Show |
chr12 | 2872223 | 2894524 |
| a0001c0001t0013 | 0/0 | 1926 | 1 | 0 | 0 | 1 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | ATTCC others(1921): Show |
chr12 | 2872223 | 2894524 |
| a0001c0001t0015 | 0/0 | 1926 | 1 | 0 | 0 | 1 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | ATTCC others(1921): Show |
chr12 | 2872223 | 2894524 |
| a0001c0001t0017 | 0/0 | 1926 | 1 | 1 | 0 | 0 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | ATTCC others(1921): Show |
chr12 | 2872223 | 2894524 |
| a0001c0001t0018 | 0/0 | 1926 | 1 | 0 | 0 | 1 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | ATTCC others(1921): Show |
chr12 | 2872223 | 2894524 |
| a0001c0001t0019 | 0/0 | 1926 | 1 | 0 | 0 | 1 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | ATTCC others(1921): Show |
chr12 | 2872223 | 2894524 |
| a0001c0001t0020 | 0/0 | 1926 | 1 | 0 | 0 | 0 | 0 | 1 | RHNO1_chr12_2872223_2894524 | RHNO1 | ATTCC others(1921): Show |
chr12 | 2872223 | 2894524 |
| a0001c0002t0001 | 1/0 | 1926 | 148 | 27 | 30 | 66 | 10 | 14 | RHNO1_chr12_2872223_2894524 | RHNO1 | ATTCC others(1921): Show |
chr12 | 2872223 | 2894524 |
| a0001c0002t0004 | 0/0 | 1926 | 8 | 0 | 0 | 8 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | ATTCC others(1921): Show |
chr12 | 2872223 | 2894524 |
| a0001c0002t0005 | 0/0 | 1926 | 5 | 0 | 3 | 1 | 1 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | ATTCC others(1921): Show |
chr12 | 2872223 | 2894524 |
| a0001c0002t0006 | 0/0 | 1926 | 3 | 2 | 0 | 0 | 0 | 1 | RHNO1_chr12_2872223_2894524 | RHNO1 | ATTCC others(1921): Show |
chr12 | 2872223 | 2894524 |
| a0001c0002t0007 | 0/0 | 1914 | 2 | 2 | 0 | 0 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | ATTCC others(1909): Show |
chr12 | 2872223 | 2894524 |
| a0001c0002t0009 | 0/0 | 1924 | 2 | 2 | 0 | 0 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | ATTCC others(1919): Show |
chr12 | 2872223 | 2894524 |
| a0001c0002t0014 | 0/0 | 1926 | 1 | 0 | 0 | 0 | 0 | 1 | RHNO1_chr12_2872223_2894524 | RHNO1 | ATTCC others(1921): Show |
chr12 | 2872223 | 2894524 |
| a0001c0004t0001 | 0/0 | 1926 | 1 | 0 | 1 | 0 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | ATTCC others(1921): Show |
chr12 | 2872223 | 2894524 |
| a0001c0006t0001 | 0/0 | 1926 | 1 | 0 | 0 | 1 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | ATTCC others(1921): Show |
chr12 | 2872223 | 2894524 |
| a0002c0003t0001 | 0/0 | 1926 | 2 | 0 | 0 | 0 | 0 | 2 | RHNO1_chr12_2872223_2894524 | RHNO1 | ATTCC others(1921): Show |
chr12 | 2872223 | 2894524 |
| a0003c0005t0016 | 0/0 | 1914 | 1 | 1 | 0 | 0 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | ATTCC others(1909): Show |
chr12 | 2872223 | 2894524 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 37 | 0 | 9 | 18 | 3 | 7 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0001t0001g0003 | 0/0 | 36 | 3 | 7 | 25 | 0 | 1 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0001t0001g0004 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0001t0001g0006 | 0/0 | 7 | 2 | 1 | 4 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0001t0001g0007 | 0/0 | 8 | 1 | 2 | 4 | 0 | 1 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0001t0001g0008 | 0/0 | 6 | 0 | 1 | 3 | 0 | 2 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0001t0001g0010 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0001t0001g0013 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0001t0001g0016 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0001t0001g0017 | 0/0 | 4 | 0 | 0 | 2 | 0 | 2 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0001t0001g0092 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0001t0002g0002 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0001t0002g0004 | 0/0 | 34 | 7 | 6 | 16 | 0 | 5 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0001t0002g0006 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0001t0002g0014 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0001t0002g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0001t0002g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0001t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0001t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0001t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0001t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0001t0002g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0001t0003g0009 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0001t0003g0015 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0001t0003g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0001t0003g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0001t0003g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0001t0003g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0001t0003g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0001t0008g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0001t0008g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0001t0010g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0001t0011g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0001t0012g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0001t0013g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0001t0015g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0001t0017g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0001t0018g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0001t0019g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0001t0020g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0002t0001g0001 | 1/0 | 58 | 10 | 11 | 31 | 4 | 1 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0002t0001g0005 | 0/0 | 11 | 1 | 6 | 3 | 0 | 1 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0002t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0002t0001g0011 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0002t0001g0012 | 0/0 | 4 | 1 | 1 | 1 | 0 | 1 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0002t0001g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0002t0001g0022 | 0/0 | 3 | 0 | 0 | 0 | 3 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0002t0001g0023 | 0/0 | 3 | 1 | 1 | 1 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0002t0001g0031 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0002t0001g0032 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0002t0001g0033 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0002t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0002t0001g0035 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0002t0001g0036 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0002t0001g0037 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0002t0001g0038 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0002t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0002t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0002t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0002t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0002t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0002t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0002t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0002t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0002t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0002t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0002t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0002t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0002t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0002t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0002t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0002t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0002t0004g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0002t0004g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0002t0004g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0002t0004g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0002t0004g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0002t0005g0001 | 0/0 | 3 | 0 | 1 | 1 | 1 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0002t0005g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0002t0005g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0002t0006g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0002t0006g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0002t0006g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0002t0007g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0002t0007g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0002t0009g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0002t0014g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0004t0001g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0001c0006t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0002c0003t0001g0003 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| a0003c0005t0016g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG00099 | hp2 | a0001 | c0002 | t0005 | g0001 | EUR | GBR | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | FIN | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG00280 | hp2 | a0001 | c0002 | t0001 | g0126 | EUR | FIN | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | CHS | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG00423 | hp1 | a0001 | c0002 | t0004 | g0001 | EAS | CHS | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG00438 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | CHS | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | CHS | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG00544 | hp2 | a0001 | c0002 | t0001 | g0045 | EAS | CHS | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG00558 | hp2 | a0001 | c0002 | t0001 | g0131 | EAS | CHS | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | CHS | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG00597 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | CHS | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | CHS | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | CHS | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG00639 | hp2 | a0001 | c0002 | t0005 | g0005 | AMR | PUR | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG00642 | hp1 | a0001 | c0002 | t0001 | g0111 | AMR | PUR | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG00642 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG00741 | hp2 | a0001 | c0002 | t0005 | g0039 | AMR | PUR | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG01069 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG01070 | hp2 | a0001 | c0002 | t0001 | g0033 | AMR | PUR | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG01074 | hp1 | a0001 | c0002 | t0001 | g0147 | AMR | PUR | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG01074 | hp2 | a0001 | c0002 | t0001 | g0011 | AMR | PUR | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG01081 | hp1 | a0001 | c0002 | t0001 | g0005 | AMR | PUR | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG01081 | hp2 | a0001 | c0002 | t0005 | g0001 | AMR | PUR | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG01106 | hp2 | a0001 | c0002 | t0001 | g0031 | AMR | PUR | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG01167 | hp1 | a0001 | c0002 | t0001 | g0123 | AMR | PUR | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG01167 | hp2 | a0001 | c0002 | t0001 | g0005 | AMR | PUR | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG01168 | hp1 | a0001 | c0002 | t0001 | g0005 | AMR | PUR | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG01175 | hp2 | a0001 | c0002 | t0001 | g0023 | AMR | PUR | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG01192 | hp1 | a0001 | c0002 | t0001 | g0038 | AMR | PUR | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG01255 | hp1 | a0001 | c0002 | t0001 | g0005 | AMR | CLM | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG01255 | hp2 | a0001 | c0002 | t0001 | g0005 | AMR | CLM | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG01257 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG01257 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG01258 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG01261 | hp1 | a0001 | c0002 | t0001 | g0012 | AMR | CLM | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG01261 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG01346 | hp1 | a0001 | c0002 | t0001 | g0127 | AMR | CLM | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG01346 | hp2 | a0001 | c0001 | t0003 | g0047 | AMR | CLM | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG01358 | hp1 | a0001 | c0002 | t0001 | g0037 | AMR | CLM | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG01358 | hp2 | a0001 | c0002 | t0001 | g0140 | AMR | CLM | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG01361 | hp1 | a0001 | c0002 | t0001 | g0005 | AMR | CLM | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG01361 | hp2 | a0001 | c0001 | t0011 | g0006 | AMR | CLM | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG01433 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0099 | AMR | CLM | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG01515 | hp2 | a0001 | c0002 | t0001 | g0022 | EUR | IBS | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG01516 | hp1 | a0001 | c0002 | t0001 | g0001 | EUR | IBS | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG01516 | hp2 | a0001 | c0002 | t0001 | g0001 | EUR | IBS | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG01517 | hp1 | a0001 | c0002 | t0001 | g0022 | EUR | IBS | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG01517 | hp2 | a0001 | c0002 | t0001 | g0001 | EUR | IBS | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG01884 | hp2 | a0001 | c0002 | t0001 | g0001 | AFR | ACB | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | ACB | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | PEL | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0059 | AMR | PEL | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG01943 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG01952 | hp1 | a0001 | c0004 | t0001 | g0001 | AMR | PEL | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | PEL | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0084 | AMR | PEL | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG02004 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG02004 | hp2 | a0001 | c0002 | t0001 | g0142 | AMR | PEL | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0052 | EAS | KHV | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG02027 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | KHV | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | KHV | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG02055 | hp1 | a0001 | c0001 | t0017 | g0085 | AFR | ACB | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG02055 | hp2 | a0001 | c0002 | t0001 | g0134 | AFR | ACB | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG02056 | hp1 | a0001 | c0002 | t0001 | g0110 | EAS | KHV | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | KHV | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | KHV | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG02074 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | KHV | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG02080 | hp1 | a0001 | c0001 | t0015 | g0081 | EAS | KHV | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG02083 | hp1 | a0001 | c0002 | t0001 | g0036 | EAS | KHV | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | KHV | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG02129 | hp2 | a0001 | c0002 | t0001 | g0011 | EAS | KHV | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | KHV | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG02145 | hp1 | a0001 | c0002 | t0001 | g0012 | AFR | ACB | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG02145 | hp2 | a0001 | c0001 | t0003 | g0020 | AFR | ACB | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0014 | AMR | PEL | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG02155 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | CDX | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG02155 | hp2 | a0001 | c0002 | t0001 | g0034 | EAS | CDX | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CDX | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG02165 | hp2 | a0001 | c0002 | t0001 | g0011 | EAS | CDX | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG02257 | hp1 | a0001 | c0002 | t0001 | g0023 | AFR | ACB | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG02257 | hp2 | a0001 | c0001 | t0003 | g0009 | AFR | ACB | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG02258 | hp1 | a0001 | c0002 | t0001 | g0128 | AFR | ACB | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | ACB | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG02273 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG02280 | hp2 | a0001 | c0001 | t0003 | g0015 | AFR | ACB | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PEL | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG02293 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0049 | AFR | ACB | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | ACB | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG02523 | hp1 | a0001 | c0002 | t0001 | g0141 | EAS | KHV | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG02572 | hp1 | a0001 | c0002 | t0001 | g0001 | AFR | GWD | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0050 | AFR | GWD | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0066 | SAS | PJL | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG02602 | hp2 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | GWD | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG02622 | hp2 | a0001 | c0002 | t0001 | g0001 | AFR | GWD | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG02630 | hp1 | a0001 | c0002 | t0001 | g0001 | AFR | GWD | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG02630 | hp2 | a0001 | c0001 | t0003 | g0020 | AFR | GWD | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | GWD | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0024 | AFR | GWD | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG02683 | hp1 | a0001 | c0002 | t0001 | g0012 | SAS | PJL | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | GWD | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG02735 | hp1 | a0001 | c0002 | t0006 | g0130 | SAS | PJL | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG02735 | hp2 | a0001 | c0001 | t0020 | g0008 | SAS | PJL | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG02809 | hp1 | a0001 | c0002 | t0001 | g0001 | AFR | GWD | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | GWD | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG02818 | hp1 | a0001 | c0001 | t0003 | g0015 | AFR | GWD | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG02818 | hp2 | a0001 | c0002 | t0001 | g0139 | AFR | GWD | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG02886 | hp1 | a0001 | c0002 | t0001 | g0001 | AFR | GWD | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG02895 | hp1 | a0001 | c0001 | t0003 | g0062 | AFR | GWD | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG02895 | hp2 | a0001 | c0002 | t0001 | g0036 | AFR | GWD | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG02897 | hp1 | a0001 | c0002 | t0001 | g0001 | AFR | GWD | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG02897 | hp2 | a0001 | c0001 | t0003 | g0009 | AFR | GWD | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG02922 | hp1 | a0001 | c0001 | t0003 | g0063 | AFR | ESN | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | ESN | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG02965 | hp1 | a0001 | c0002 | t0001 | g0137 | AFR | ESN | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG02965 | hp2 | a0001 | c0002 | t0001 | g0044 | AFR | ESN | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | ESN | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | ESN | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG02976 | hp1 | a0001 | c0002 | t0001 | g0001 | AFR | ESN | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG02976 | hp2 | a0001 | c0001 | t0003 | g0009 | AFR | ESN | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0004 | SAS | PJL | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0086 | AFR | GWD | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | GWD | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG03098 | hp2 | a0001 | c0002 | t0009 | g0030 | AFR | MSL | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG03130 | hp1 | a0001 | c0001 | t0003 | g0009 | AFR | ESN | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | ESN | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG03195 | hp1 | a0001 | c0002 | t0001 | g0129 | AFR | ESN | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG03195 | hp2 | a0001 | c0002 | t0001 | g0010 | AFR | ESN | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | MSL | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | MSL | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG03225 | hp1 | a0001 | c0002 | t0001 | g0001 | AFR | MSL | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | MSL | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG03239 | hp1 | a0001 | c0002 | t0001 | g0005 | SAS | PJL | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0043 | AFR | MSL | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG03453 | hp2 | a0001 | c0002 | t0007 | g0106 | AFR | MSL | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | MSL | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | MSL | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG03490 | hp2 | a0001 | c0002 | t0001 | g0035 | SAS | PJL | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG03491 | hp1 | a0002 | c0003 | t0001 | g0003 | SAS | PJL | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG03491 | hp2 | a0001 | c0002 | t0001 | g0145 | SAS | PJL | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG03492 | hp1 | a0002 | c0003 | t0001 | g0003 | SAS | PJL | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG03492 | hp2 | a0001 | c0002 | t0001 | g0035 | SAS | PJL | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG03516 | hp1 | a0001 | c0002 | t0007 | g0105 | AFR | ESN | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG03516 | hp2 | a0001 | c0001 | t0003 | g0009 | AFR | ESN | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG03540 | hp1 | a0001 | c0001 | t0003 | g0009 | AFR | GWD | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG03579 | hp1 | a0001 | c0002 | t0001 | g0001 | AFR | MSL | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG03579 | hp2 | a0001 | c0002 | t0001 | g0104 | AFR | MSL | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0004 | SAS | PJL | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0079 | SAS | PJL | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG03688 | hp1 | a0001 | c0002 | t0001 | g0093 | SAS | STU | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG03688 | hp2 | a0001 | c0002 | t0001 | g0144 | SAS | STU | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0004 | SAS | PJL | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0004 | SAS | PJL | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG03710 | hp1 | a0001 | c0002 | t0001 | g0124 | SAS | PJL | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG03710 | hp2 | a0001 | c0002 | t0001 | g0146 | SAS | PJL | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG03834 | hp1 | a0001 | c0002 | t0001 | g0143 | SAS | BEB | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0017 | SAS | BEB | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0018 | SAS | BEB | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0004 | SAS | BEB | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG03942 | hp1 | a0001 | c0002 | t0001 | g0119 | SAS | BEB | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG03942 | hp2 | a0001 | c0002 | t0001 | g0032 | SAS | BEB | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | STU | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | STU | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG04184 | hp1 | a0001 | c0002 | t0001 | g0120 | SAS | BEB | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0014 | SAS | BEB | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0018 | SAS | STU | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG04204 | hp1 | a0001 | c0002 | t0014 | g0001 | SAS | STU | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | STU | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA18522 | hp1 | a0001 | c0002 | t0001 | g0031 | AFR | YRI | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA18522 | hp2 | a0001 | c0001 | t0003 | g0015 | AFR | YRI | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | CHB | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0024 | AFR | YRI | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | YRI | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA18939 | hp1 | a0001 | c0001 | t0008 | g0007 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA18939 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA18941 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA18942 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA18943 | hp1 | a0001 | c0002 | t0001 | g0108 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA18944 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA18946 | hp1 | a0001 | c0002 | t0001 | g0135 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA18946 | hp2 | a0001 | c0002 | t0001 | g0117 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA18947 | hp1 | a0001 | c0002 | t0005 | g0001 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA18950 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA18956 | hp1 | a0001 | c0001 | t0008 | g0028 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA18956 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA18959 | hp1 | a0001 | c0002 | t0001 | g0023 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA18960 | hp1 | a0001 | c0002 | t0001 | g0118 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA18962 | hp2 | a0001 | c0002 | t0001 | g0037 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA18963 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA18965 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA18965 | hp2 | a0001 | c0002 | t0004 | g0012 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA18966 | hp1 | a0001 | c0001 | t0019 | g0003 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA18966 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA18968 | hp1 | a0001 | c0002 | t0004 | g0125 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA18968 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA18974 | hp2 | a0001 | c0002 | t0004 | g0001 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA18975 | hp2 | a0001 | c0002 | t0001 | g0136 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA18977 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA18978 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA18979 | hp1 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA18980 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA18983 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA18985 | hp1 | a0001 | c0002 | t0001 | g0114 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA18988 | hp2 | a0001 | c0002 | t0001 | g0132 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA18991 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA18995 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA18997 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA18997 | hp2 | a0001 | c0002 | t0001 | g0021 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA18998 | hp2 | a0001 | c0002 | t0001 | g0021 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA18999 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA19001 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA19005 | hp1 | a0001 | c0002 | t0004 | g0011 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA19005 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA19009 | hp2 | a0001 | c0002 | t0004 | g0034 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA19010 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA19010 | hp2 | a0001 | c0001 | t0018 | g0002 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | LWK | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA19030 | hp2 | a0001 | c0002 | t0001 | g0101 | AFR | LWK | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA19043 | hp1 | a0001 | c0001 | t0010 | g0097 | AFR | LWK | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA19043 | hp2 | a0003 | c0005 | t0016 | g0107 | AFR | LWK | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA19054 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA19059 | hp1 | a0001 | c0002 | t0004 | g0001 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA19059 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA19060 | hp2 | a0001 | c0002 | t0001 | g0021 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA19063 | hp2 | a0001 | c0002 | t0001 | g0121 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA19064 | hp2 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA19067 | hp1 | a0001 | c0002 | t0001 | g0122 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA19067 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA19068 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA19070 | hp1 | a0001 | c0001 | t0013 | g0003 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA19070 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA19072 | hp1 | a0001 | c0002 | t0001 | g0138 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA19072 | hp2 | a0001 | c0002 | t0001 | g0109 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA19074 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA19075 | hp1 | a0001 | c0001 | t0012 | g0055 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA19075 | hp2 | a0001 | c0002 | t0001 | g0112 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA19077 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA19078 | hp1 | a0001 | c0006 | t0001 | g0025 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA19079 | hp1 | a0001 | c0002 | t0004 | g0001 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA19079 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA19080 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA19081 | hp1 | a0001 | c0002 | t0001 | g0116 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA19083 | hp2 | a0001 | c0002 | t0001 | g0113 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA19084 | hp1 | a0001 | c0002 | t0001 | g0012 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA19084 | hp2 | a0001 | c0002 | t0001 | g0032 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA19085 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA19088 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA19089 | hp1 | a0001 | c0002 | t0001 | g0033 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA19089 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA19240 | hp1 | a0001 | c0002 | t0006 | g0102 | AFR | YRI | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | YRI | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA20129 | hp1 | a0001 | c0001 | t0003 | g0064 | AFR | ASW | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ASW | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA20752 | hp1 | a0001 | c0002 | t0001 | g0022 | EUR | TSI | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA20752 | hp2 | a0001 | c0002 | t0001 | g0001 | EUR | TSI | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA20805 | hp1 | a0001 | c0002 | t0001 | g0115 | EUR | TSI | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA20805 | hp2 | a0001 | c0002 | t0001 | g0133 | EUR | TSI | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | GIH | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | GIH | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG02109 | hp1 | a0001 | c0002 | t0001 | g0098 | AFR | ACB | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG02109 | hp2 | a0001 | c0001 | t0003 | g0020 | AFR | ACB | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | ACB | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | ACB | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG02559 | hp1 | a0001 | c0002 | t0001 | g0038 | AFR | ACB | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | ACB | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | MSL | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG03471 | hp2 | a0001 | c0002 | t0006 | g0103 | AFR | MSL | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG06807 | hp1 | a0001 | c0002 | t0001 | g0005 | AFR | USA | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| HG06807 | hp2 | a0001 | c0002 | t0009 | g0030 | AFR | USA | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA20300 | hp1 | a0001 | c0001 | t0003 | g0015 | AFR | USA | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | USA | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0148 | AFR | LWK | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| NA21309 | hp2 | a0001 | c0002 | t0001 | g0100 | AFR | LWK | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0092 | REF | REF | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0001 | g0001 | REF | REF | RHNO1_chr12_2872223_2894524 | RHNO1 | chr12 | 2872223 | 2894524 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:2887975 | G | A | 1 | a0003 | 1 | NA19043.hp2 | missense_variant | MODERATE | c.233G>A | p.Arg78Gln | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 3/3 | 377/1926 | 233/717 | 78/238 | chr12 | 2887975 | |||
| chr12:2888137 | T | G | 1 | a0002 | 2 | HG03491.hp1 HG03492.hp1 |
missense_variant | MODERATE | c.395T>G | p.Leu132Arg | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 3/3 | 539/1926 | 395/717 | 132/238 | chr12 | 2888137 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:2885396 | T | C | 1 | a0001c0004 | 1 | HG01952.hp1 | synonymous_variant | LOW | c.30T>C | p.Pro10Pro | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 2/3 | 174/1926 | 30/717 | 10/238 | chr12 | 2885396 | |||
| chr12:2885433 | C | T | 1 | a0001c0006 | 1 | NA19078.hp1 | synonymous_variant | LOW | c.67C>T | p.Leu23Leu | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 2/3 | 211/1926 | 67/717 | 23/238 | chr12 | 2885433 | |||
| chr12:2888231 | G | A | 3 | a0001c0001 a0001c0006 a0002c0003 |
254 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(251): Show |
synonymous_variant | LOW | c.489G>A | p.Ser163Ser | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 3/3 | 633/1926 | 489/717 | 163/238 | chr12 | 2888231 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:2877252 | C | G | 1 | a0001c0001t0020 | 1 | HG02735.hp2 | 5_prime_UTR_variant | MODIFIER | c.-115C>G | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/3 | 8115 | chr12 | 2877252 | ||||||
| chr12:2877259 | T | C | 1 | a0001c0002t0004 | 8 | HG00423.hp1 NA18965.hp2 NA18968.hp1 others(5): Show |
5_prime_UTR_variant | MODIFIER | c.-108T>C | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/3 | 8108 | chr12 | 2877259 | ||||||
| chr12:2877277 | G | A | 1 | a0001c0001t0010 | 1 | NA19043.hp1 | 5_prime_UTR_variant | MODIFIER | c.-90G>A | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/3 | 8090 | chr12 | 2877277 | ||||||
| chr12:2885352 | C | G | 1 | a0001c0001t0019 | 1 | NA18966.hp1 | 5_prime_UTR_variant | MODIFIER | c.-15C>G | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 2/3 | 15 | chr12 | 2885352 | ||||||
| chr12:2885362 | G | A | 1 | a0001c0001t0011 | 1 | HG01361.hp2 | 5_prime_UTR_variant | MODIFIER | c.-5G>A | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 2/3 | 5 | chr12 | 2885362 | ||||||
| chr12:2888719 | G | A | 1 | a0001c0002t0007 | 2 | HG03453.hp2 HG03516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*260G>A | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 3/3 | 260 | chr12 | 2888719 | ||||||
| chr12:2888737 | C | T | 1 | a0001c0001t0018 | 1 | NA19010.hp2 | 3_prime_UTR_variant | MODIFIER | c.*278C>T | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 3/3 | 278 | chr12 | 2888737 | ||||||
| chr12:2888773 | G | T | 2 | a0001c0001t0002 a0001c0001t0003 |
79 | HG00597.hp1 HG00621.hp1 HG00735.hp1 others(76): Show |
3_prime_UTR_variant | MODIFIER | c.*314G>T | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 3/3 | 314 | chr12 | 2888773 | ||||||
| chr12:2888774 | C | T | 2 | a0001c0001t0002 a0001c0001t0003 |
79 | HG00597.hp1 HG00621.hp1 HG00735.hp1 others(76): Show |
3_prime_UTR_variant | MODIFIER | c.*315C>T | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 3/3 | 315 | chr12 | 2888774 | ||||||
| chr12:2888853 | G | T | 1 | a0001c0001t0017 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*394G>T | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 3/3 | 394 | chr12 | 2888853 | ||||||
| chr12:2889036 | C | T | 2 | a0001c0002t0004 a0001c0002t0005 |
13 | HG00099.hp2 HG00423.hp1 HG00639.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*577C>T | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 3/3 | 577 | chr12 | 2889036 | ||||||
| chr12:2889095 | C | T | 3 | a0001c0002t0007 a0001c0002t0009 a0003c0005t0016 |
5 | HG03098.hp2 HG03453.hp2 HG03516.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*636C>T | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 3/3 | 636 | chr12 | 2889095 | ||||||
| chr12:2889127 | C | T | 1 | a0001c0001t0015 | 1 | HG02080.hp1 | 3_prime_UTR_variant | MODIFIER | c.*668C>T | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 3/3 | 668 | chr12 | 2889127 | ||||||
| chr12:2889161 | ACT | A | 3 | a0001c0002t0007 a0001c0002t0009 a0003c0005t0016 |
5 | HG03098.hp2 HG03453.hp2 HG03516.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*705_*706delCT | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 3/3 | 705 | INFO_REALIGN_3_PRIME | chr12 | 2889161 | |||||
| chr12:2889239 | G | A | 1 | a0001c0001t0008 | 2 | NA18939.hp1 NA18956.hp1 |
3_prime_UTR_variant | MODIFIER | c.*780G>A | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 3/3 | 780 | chr12 | 2889239 | ||||||
| chr12:2889260 | GAGGGGAG others(3): Show |
G | 2 | a0001c0002t0007 a0003c0005t0016 |
3 | HG03453.hp2 HG03516.hp1 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*807_*816delAGATAA others(4): Show |
RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 3/3 | 807 | INFO_REALIGN_3_PRIME | chr12 | 2889260 | |||||
| chr12:2889293 | T | C | 1 | a0001c0001t0002 | 62 | HG00597.hp1 HG00621.hp1 HG00735.hp1 others(59): Show |
3_prime_UTR_variant | MODIFIER | c.*834T>C | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 3/3 | 834 | chr12 | 2889293 | ||||||
| chr12:2889301 | C | T | 1 | a0001c0002t0006 | 3 | HG02735.hp1 HG03471.hp2 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*842C>T | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 3/3 | 842 | chr12 | 2889301 | ||||||
| chr12:2889393 | T | G | 1 | a0001c0001t0012 | 1 | NA19075.hp1 | 3_prime_UTR_variant | MODIFIER | c.*934T>G | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 3/3 | 934 | chr12 | 2889393 | ||||||
| chr12:2889453 | C | G | 3 | a0001c0002t0007 a0001c0002t0009 a0003c0005t0016 |
5 | HG03098.hp2 HG03453.hp2 HG03516.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*994C>G | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 3/3 | 994 | chr12 | 2889453 | ||||||
| chr12:2889455 | A | C | 1 | a0001c0002t0014 | 1 | HG04204.hp1 | 3_prime_UTR_variant | MODIFIER | c.*996A>C | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 3/3 | 996 | chr12 | 2889455 | ||||||
| chr12:2889507 | C | G | 1 | a0001c0001t0013 | 1 | NA19070.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1048C>G | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 3/3 | 1048 | chr12 | 2889507 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:2877284 | T | G | 1 | a0001c0002t0005g0039 | 1 | HG00741.hp2 | splice_donor_variant&intron_variant | HIGH | c.-85+2T>G | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | chr12 | 2877284 | |||||||
| chr12:2877289 | C | T | 1 | a0001c0001t0001g0149 | 1 | HG02723.hp2 | splice_region_variant&intron_variant | LOW | c.-85+7C>T | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | chr12 | 2877289 | |||||||
| chr12:2877312 | GGAA | G | 4 | a0001c0001t0001g0013 a0001c0001t0001g0040 a0001c0001t0001g0041 others(1): Show |
7 | HG01109.hp2 HG01891.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.-85+35_-85+37delAA others(1): Show |
RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 2877312 | ||||||
| chr12:2877316 | G | A | 4 | a0001c0001t0001g0013 a0001c0001t0001g0040 a0001c0001t0001g0041 others(1): Show |
7 | HG01109.hp2 HG01891.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.-85+34G>A | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | chr12 | 2877316 | |||||||
| chr12:2877397 | C | T | 1 | a0001c0001t0002g0148 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-85+115C>T | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | chr12 | 2877397 | |||||||
| chr12:2877429 | C | T | 1 | a0001c0002t0001g0147 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-85+147C>T | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | chr12 | 2877429 | |||||||
| chr12:2877437 | T | C | 107 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(104): Show |
271 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(268): Show |
intron_variant | MODIFIER | c.-85+155T>C | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | chr12 | 2877437 | |||||||
| chr12:2877509 | C | G | 11 | a0001c0001t0001g0099 a0001c0002t0001g0031 a0001c0002t0001g0098 others(8): Show |
12 | HG01106.hp2 HG01496.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.-85+227C>G | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | chr12 | 2877509 | |||||||
| chr12:2877612 | CG | C | 7 | a0001c0002t0001g0104 a0001c0002t0006g0102 a0001c0002t0006g0103 others(4): Show |
8 | HG03098.hp2 HG03453.hp2 HG03471.hp2 others(5): Show |
intron_variant | MODIFIER | c.-85+331delG | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | chr12 | 2877612 | |||||||
| chr12:2877667 | A | G | 3 | a0001c0001t0010g0097 a0001c0002t0001g0100 a0001c0002t0001g0101 |
3 | NA19030.hp2 NA19043.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-85+385A>G | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | chr12 | 2877667 | |||||||
| chr12:2877739 | T | C | 1 | a0001c0001t0002g0043 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-85+457T>C | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | chr12 | 2877739 | |||||||
| chr12:2877745 | G | T | 104 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(101): Show |
268 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(265): Show |
intron_variant | MODIFIER | c.-85+463G>T | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | chr12 | 2877745 | |||||||
| chr12:2877747 | C | T | 1 | a0001c0001t0001g0096 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-85+465C>T | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | chr12 | 2877747 | |||||||
| chr12:2877836 | C | T | 1 | a0001c0001t0001g0099 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-85+554C>T | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | chr12 | 2877836 | |||||||
| chr12:2877899 | G | A | 2 | a0001c0002t0001g0100 a0001c0002t0001g0101 |
2 | NA19030.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-85+617G>A | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | chr12 | 2877899 | |||||||
| chr12:2877935 | C | A | 1 | a0001c0001t0001g0046 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.-85+653C>A | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | chr12 | 2877935 | |||||||
| chr12:2877975 | G | A | 2 | a0001c0001t0002g0024 a0001c0001t0002g0043 |
3 | HG02647.hp2 HG03453.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-85+693G>A | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | chr12 | 2877975 | |||||||
| chr12:2877992 | C | G | 3 | a0001c0001t0001g0010 a0001c0001t0001g0095 a0001c0002t0001g0010 |
7 | HG01891.hp2 HG02615.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.-85+710C>G | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | chr12 | 2877992 | |||||||
| chr12:2878036 | G | A | 2 | a0001c0002t0001g0108 a0001c0002t0001g0109 |
2 | NA18943.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.-85+754G>A | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | chr12 | 2878036 | |||||||
| chr12:2878073 | G | A | 2 | a0001c0002t0006g0102 a0001c0002t0006g0103 |
2 | HG03471.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-85+791G>A | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | chr12 | 2878073 | |||||||
| chr12:2878114 | G | A | 92 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(89): Show |
254 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(251): Show |
intron_variant | MODIFIER | c.-85+832G>A | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | chr12 | 2878114 | |||||||
| chr12:2878143 | G | A | 2 | a0001c0002t0001g0031 a0001c0002t0001g0098 |
3 | HG01106.hp2 HG02109.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-85+861G>A | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | chr12 | 2878143 | |||||||
| chr12:2878255 | T | A | 1 | a0001c0001t0003g0047 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-85+973T>A | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | chr12 | 2878255 | |||||||
| chr12:2878302 | GATCTGAT others(4349): Show |
G | 1 | a0001c0001t0001g0149 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-85+1022_-84-2624d others(2): Show |
RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 2878302 | ||||||
| chr12:2878396 | A | G | 1 | a0001c0001t0001g0002 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.-85+1114A>G | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | chr12 | 2878396 | |||||||
| chr12:2878408 | A | G | 92 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(89): Show |
254 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(251): Show |
intron_variant | MODIFIER | c.-85+1126A>G | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | chr12 | 2878408 | |||||||
| chr12:2878432 | T | C | 1 | a0001c0001t0002g0004 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-85+1150T>C | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | chr12 | 2878432 | |||||||
| chr12:2878437 | C | G | 2 | a0001c0002t0001g0031 a0001c0002t0001g0098 |
3 | HG01106.hp2 HG02109.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-85+1155C>G | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | chr12 | 2878437 | |||||||
| chr12:2878500 | G | T | 1 | a0001c0001t0001g0003 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-85+1218G>T | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | chr12 | 2878500 | |||||||
| chr12:2878602 | G | A | 1 | a0001c0001t0010g0097 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-85+1320G>A | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | chr12 | 2878602 | |||||||
| chr12:2878698 | G | C | 1 | a0001c0001t0001g0006 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-85+1416G>C | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | chr12 | 2878698 | |||||||
| chr12:2878778 | T | G | 26 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(23): Show |
78 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.-85+1496T>G | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | chr12 | 2878778 | |||||||
| chr12:2878829 | C | T | 4 | a0001c0002t0007g0105 a0001c0002t0007g0106 a0001c0002t0009g0030 others(1): Show |
5 | HG03098.hp2 HG03453.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.-85+1547C>T | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | chr12 | 2878829 | |||||||
| chr12:2878969 | GT | G | 92 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(89): Show |
254 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(251): Show |
intron_variant | MODIFIER | c.-85+1697delT | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 2878969 | ||||||
| chr12:2878979 | T | A | 2 | a0001c0002t0001g0022 a0003c0005t0016g0107 |
2 | NA19043.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-85+1697T>A | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | chr12 | 2878979 | |||||||
| chr12:2879210 | C | G | 1 | a0001c0001t0001g0013 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-85+1928C>G | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | chr12 | 2879210 | |||||||
| chr12:2879243 | A | G | 1 | a0001c0001t0001g0003 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.-85+1961A>G | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | chr12 | 2879243 | |||||||
| chr12:2879297 | C | T | 1 | a0001c0002t0001g0100 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-85+2015C>T | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | chr12 | 2879297 | |||||||
| chr12:2879298 | G | A | 3 | a0001c0001t0001g0010 a0001c0001t0001g0095 a0001c0002t0001g0010 |
7 | HG01891.hp2 HG02615.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.-85+2016G>A | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | chr12 | 2879298 | |||||||
| chr12:2879327 | A | AT | 92 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(89): Show |
253 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(250): Show |
intron_variant | MODIFIER | c.-85+2054dupT | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 2879327 | ||||||
| chr12:2879395 | C | G | 1 | a0001c0001t0001g0006 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-85+2113C>G | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | chr12 | 2879395 | |||||||
| chr12:2879468 | G | A | 2 | a0001c0001t0002g0024 a0001c0001t0002g0043 |
3 | HG02647.hp2 HG03453.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-85+2186G>A | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | chr12 | 2879468 | |||||||
| chr12:2879612 | G | GCTGGGAT others(2): Show |
3 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0017 |
5 | HG00423.hp2 NA18984.hp1 NA18988.hp1 others(2): Show |
intron_variant | MODIFIER | c.-85+2331_-85+2332i others(11): Show |
RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 2879612 | ||||||
| chr12:2879614 | G | A | 3 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0017 |
5 | HG00423.hp2 NA18984.hp1 NA18988.hp1 others(2): Show |
intron_variant | MODIFIER | c.-85+2332G>A | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | chr12 | 2879614 | |||||||
| chr12:2879614 | G | C | 1 | a0001c0001t0001g0029 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.-85+2332G>C | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | chr12 | 2879614 | |||||||
| chr12:2879615 | T | A | 1 | a0001c0001t0001g0029 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.-85+2333T>A | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | chr12 | 2879615 | |||||||
| chr12:2879615 | T | G | 3 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0017 |
5 | HG00423.hp2 NA18984.hp1 NA18988.hp1 others(2): Show |
intron_variant | MODIFIER | c.-85+2333T>G | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | chr12 | 2879615 | |||||||
| chr12:2879626 | G | A | 1 | a0001c0002t0001g0022 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.-85+2344G>A | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | chr12 | 2879626 | |||||||
| chr12:2879810 | T | A | 2 | a0001c0002t0001g0100 a0001c0002t0001g0101 |
2 | NA19030.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-85+2528T>A | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | chr12 | 2879810 | |||||||
| chr12:2880191 | C | T | 1 | a0001c0002t0001g0136 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.-85+2909C>T | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | chr12 | 2880191 | |||||||
| chr12:2880333 | C | G | 4 | a0001c0001t0001g0013 a0001c0001t0001g0040 a0001c0001t0001g0041 others(1): Show |
7 | HG01109.hp2 HG01891.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.-85+3051C>G | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | chr12 | 2880333 | |||||||
| chr12:2880420 | C | A | 1 | a0001c0001t0002g0014 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-85+3138C>A | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | chr12 | 2880420 | |||||||
| chr12:2880530 | T | A | 7 | a0001c0001t0003g0009 a0001c0001t0003g0015 a0001c0001t0003g0020 others(4): Show |
17 | HG01346.hp2 HG02109.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.-85+3248T>A | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | chr12 | 2880530 | |||||||
| chr12:2880591 | G | C | 2 | a0001c0001t0002g0004 a0001c0001t0002g0019 |
3 | NA18951.hp1 NA18997.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.-85+3309G>C | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | chr12 | 2880591 | |||||||
| chr12:2880637 | C | CTTTA | 9 | a0001c0001t0001g0099 a0001c0002t0001g0100 a0001c0002t0001g0101 others(6): Show |
10 | HG01496.hp1 HG03098.hp2 HG03453.hp2 others(7): Show |
intron_variant | MODIFIER | c.-85+3367_-85+3370d others(6): Show |
RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 2880637 | ||||||
| chr12:2880662 | G | A | 2 | a0001c0002t0001g0022 a0001c0002t0001g0140 |
3 | HG01358.hp2 HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.-85+3380G>A | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | chr12 | 2880662 | |||||||
| chr12:2880745 | C | T | 1 | a0001c0002t0001g0101 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-85+3463C>T | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | chr12 | 2880745 | |||||||
| chr12:2880777 | G | A | 6 | a0001c0002t0001g0005 a0001c0002t0001g0021 a0001c0002t0001g0032 others(3): Show |
6 | NA18943.hp1 NA18946.hp2 NA18997.hp2 others(3): Show |
intron_variant | MODIFIER | c.-85+3495G>A | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | chr12 | 2880777 | |||||||
| chr12:2880836 | T | A | 102 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(99): Show |
266 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(263): Show |
intron_variant | MODIFIER | c.-85+3554T>A | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | chr12 | 2880836 | |||||||
| chr12:2881030 | C | A | 3 | a0001c0002t0004g0001 a0001c0002t0004g0011 a0001c0002t0004g0012 |
4 | NA18965.hp2 NA18974.hp2 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.-85+3748C>A | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | chr12 | 2881030 | |||||||
| chr12:2881156 | G | A | 2 | a0001c0002t0006g0102 a0001c0002t0006g0103 |
2 | HG03471.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-85+3874G>A | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | chr12 | 2881156 | |||||||
| chr12:2881235 | A | T | 91 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(88): Show |
253 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(250): Show |
intron_variant | MODIFIER | c.-85+3953A>T | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | chr12 | 2881235 | |||||||
| chr12:2881268 | A | C | 1 | a0001c0001t0003g0009 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-85+3986A>C | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | chr12 | 2881268 | |||||||
| chr12:2881645 | G | A | 4 | a0001c0002t0007g0105 a0001c0002t0007g0106 a0001c0002t0009g0030 others(1): Show |
5 | HG03098.hp2 HG03453.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.-84-3638G>A | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | chr12 | 2881645 | |||||||
| chr12:2881717 | C | T | 1 | a0001c0001t0002g0004 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.-84-3566C>T | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | chr12 | 2881717 | |||||||
| chr12:2881733 | C | T | 1 | a0001c0001t0002g0004 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-84-3550C>T | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | chr12 | 2881733 | |||||||
| chr12:2881819 | C | T | 1 | a0001c0002t0009g0030 | 2 | HG03098.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-84-3464C>T | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | chr12 | 2881819 | |||||||
| chr12:2881902 | CA | C | 5 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0040 others(2): Show |
8 | HG01109.hp2 HG01891.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.-84-3367delA | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 2881902 | ||||||
| chr12:2881913 | A | G | 2 | a0001c0002t0007g0105 a0001c0002t0007g0106 |
2 | HG03453.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-84-3370A>G | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | chr12 | 2881913 | |||||||
| chr12:2882108 | C | T | 2 | a0001c0002t0001g0100 a0001c0002t0001g0101 |
2 | NA19030.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-84-3175C>T | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | chr12 | 2882108 | |||||||
| chr12:2882278 | C | CAATA | 15 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(12): Show |
25 | HG01167.hp1 HG01167.hp2 HG01255.hp2 others(22): Show |
intron_variant | MODIFIER | c.-84-2970_-84-2967d others(6): Show |
RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 2882278 | ||||||
| chr12:2882278 | C | CAATAAAT others(1): Show |
3 | a0001c0001t0001g0018 a0001c0002t0001g0001 a0001c0002t0001g0044 |
4 | HG00597.hp2 HG02129.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.-84-2974_-84-2967d others(10): Show |
RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 2882278 | ||||||
| chr12:2882278 | CAATA | C | 3 | a0001c0001t0001g0089 a0001c0001t0002g0004 a0001c0002t0001g0104 |
3 | HG00621.hp1 HG03579.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.-84-2970_-84-2967d others(6): Show |
RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 2882278 | ||||||
| chr12:2882278 | CAATAAAT others(1): Show |
C | 74 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(71): Show |
179 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(176): Show |
intron_variant | MODIFIER | c.-84-2974_-84-2967d others(10): Show |
RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 2882278 | ||||||
| chr12:2882278 | CAATAAAT others(5): Show |
C | 8 | a0001c0001t0001g0010 a0001c0001t0001g0095 a0001c0001t0017g0085 others(5): Show |
12 | HG01891.hp2 HG02055.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.-84-2978_-84-2967d others(14): Show |
RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 2882278 | ||||||
| chr12:2882511 | TG | T | 1 | a0001c0001t0001g0013 | 3 | HG01109.hp2 HG02622.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-84-2770delG | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 2882511 | ||||||
| chr12:2882561 | A | C | 1 | a0001c0001t0001g0002 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-84-2722A>C | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | chr12 | 2882561 | |||||||
| chr12:2882678 | GGACGAAA others(6): Show |
G | 1 | a0001c0001t0001g0149 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-84-2601_-84-2589d others(15): Show |
RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 2882678 | ||||||
| chr12:2882754 | T | C | 1 | a0001c0001t0001g0048 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.-84-2529T>C | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | chr12 | 2882754 | |||||||
| chr12:2882757 | T | TTA | 4 | a0001c0002t0007g0105 a0001c0002t0007g0106 a0001c0002t0009g0030 others(1): Show |
5 | HG03098.hp2 HG03453.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.-84-2526_-84-2525i others(4): Show |
RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | chr12 | 2882757 | |||||||
| chr12:2882846 | G | A | 2 | a0001c0001t0002g0049 a0001c0001t0002g0050 |
2 | HG02451.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.-84-2437G>A | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | chr12 | 2882846 | |||||||
| chr12:2882897 | A | G | 93 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(90): Show |
255 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(252): Show |
intron_variant | MODIFIER | c.-84-2386A>G | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | chr12 | 2882897 | |||||||
| chr12:2883014 | C | A | 2 | a0001c0002t0006g0102 a0001c0002t0006g0103 |
2 | HG03471.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-84-2269C>A | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | chr12 | 2883014 | |||||||
| chr12:2883022 | A | G | 4 | a0001c0002t0001g0143 a0001c0002t0001g0144 a0001c0002t0001g0145 others(1): Show |
4 | HG03491.hp2 HG03688.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.-84-2261A>G | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | chr12 | 2883022 | |||||||
| chr12:2883066 | C | CA | 11 | a0001c0002t0001g0021 a0001c0002t0001g0031 a0001c0002t0001g0032 others(8): Show |
15 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(12): Show |
intron_variant | MODIFIER | c.-84-2198dupA | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 2883066 | ||||||
| chr12:2883070 | A | AAAAAAAA others(7): Show |
1 | a0001c0001t0001g0013 | 4 | HG01109.hp2 HG02622.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-84-2200_-84-2199i others(16): Show |
RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 2883070 | ||||||
| chr12:2883070 | A | AAAAAAAA others(7): Show |
2 | a0001c0001t0001g0040 a0001c0001t0001g0041 |
2 | HG01891.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-84-2205_-84-2204i others(16): Show |
RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 2883070 | ||||||
| chr12:2883070 | A | AAAAAAAC others(7): Show |
1 | a0001c0001t0001g0042 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-84-2207_-84-2206i others(16): Show |
RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 2883070 | ||||||
| chr12:2883072 | A | AAAAAAAA others(5): Show |
1 | a0001c0001t0001g0060 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-84-2200_-84-2199i others(14): Show |
RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 2883072 | ||||||
| chr12:2883072 | A | AAAAAACA others(5): Show |
1 | a0001c0001t0001g0149 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-84-2206_-84-2205i others(14): Show |
RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 2883072 | ||||||
| chr12:2883074 | A | AAAAAAAA others(7): Show |
1 | a0001c0001t0002g0053 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-84-2199_-84-2198i others(16): Show |
RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 2883074 | ||||||
| chr12:2883074 | A | AAAAAAAA others(6): Show |
3 | a0001c0001t0001g0061 a0001c0001t0003g0015 a0001c0001t0003g0020 |
8 | HG02109.hp2 HG02145.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.-84-2200_-84-2199i others(15): Show |
RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 2883074 | ||||||
| chr12:2883074 | A | AAAAAAAA others(5): Show |
1 | a0001c0001t0001g0090 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-84-2201_-84-2200i others(14): Show |
RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 2883074 | ||||||
| chr12:2883075 | A | AAAAAAAA others(7): Show |
2 | a0001c0001t0002g0051 a0001c0001t0002g0052 |
2 | HG02027.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.-84-2196_-84-2195i others(16): Show |
RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 2883075 | ||||||
| chr12:2883075 | A | AAAAAAAA others(6): Show |
16 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0018 others(13): Show |
56 | HG00597.hp1 HG00621.hp1 HG00735.hp1 others(53): Show |
intron_variant | MODIFIER | c.-84-2199_-84-2198i others(15): Show |
RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 2883075 | ||||||
| chr12:2883075 | A | AAAAAAAA others(5): Show |
62 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(59): Show |
176 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(173): Show |
intron_variant | MODIFIER | c.-84-2200_-84-2199i others(14): Show |
RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 2883075 | ||||||
| chr12:2883075 | A | AAAAAAAA others(7): Show |
1 | a0001c0001t0002g0091 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.-84-2201_-84-2200i others(16): Show |
RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 2883075 | ||||||
| chr12:2883075 | A | AAAACAAA others(5): Show |
1 | a0001c0001t0001g0099 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-84-2205_-84-2204i others(14): Show |
RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 2883075 | ||||||
| chr12:2883084 | A | AAAAAAAA others(5): Show |
2 | a0001c0002t0006g0102 a0001c0002t0006g0103 |
2 | HG03471.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-84-2198_-84-2197i others(14): Show |
RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 2883084 | ||||||
| chr12:2883084 | A | C | 1 | a0003c0005t0016g0107 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-84-2199A>C | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | chr12 | 2883084 | |||||||
| chr12:2883150 | G | A | 2 | a0001c0002t0006g0102 a0001c0002t0006g0103 |
2 | HG03471.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-84-2133G>A | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | chr12 | 2883150 | |||||||
| chr12:2883233 | C | T | 1 | a0001c0002t0001g0142 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-84-2050C>T | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | chr12 | 2883233 | |||||||
| chr12:2883325 | A | G | 93 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(90): Show |
255 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(252): Show |
intron_variant | MODIFIER | c.-84-1958A>G | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | chr12 | 2883325 | |||||||
| chr12:2883476 | A | AAT | 2 | a0001c0002t0001g0023 a0001c0002t0001g0131 |
4 | HG00558.hp2 HG01175.hp2 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.-84-1772_-84-1771d others(4): Show |
RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 2883476 | ||||||
| chr12:2883476 | A | AATATAT | 2 | a0001c0002t0001g0036 a0001c0002t0006g0130 |
3 | HG02083.hp1 HG02735.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.-84-1776_-84-1771d others(8): Show |
RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 2883476 | ||||||
| chr12:2883476 | A | AATATATA others(1): Show |
4 | a0001c0002t0001g0035 a0001c0002t0001g0129 a0001c0002t0001g0144 others(1): Show |
5 | HG03195.hp1 HG03490.hp2 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.-84-1778_-84-1771d others(10): Show |
RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 2883476 | ||||||
| chr12:2883476 | A | AATATATA others(3): Show |
3 | a0001c0002t0001g0112 a0001c0002t0001g0127 a0001c0002t0001g0128 |
3 | HG01346.hp1 HG02258.hp1 NA19075.hp2 |
intron_variant | MODIFIER | c.-84-1780_-84-1771d others(12): Show |
RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 2883476 | ||||||
| chr12:2883476 | A | AATATATA others(5): Show |
7 | a0001c0002t0001g0034 a0001c0002t0001g0108 a0001c0002t0001g0111 others(4): Show |
7 | HG00280.hp2 HG00642.hp1 HG02155.hp2 others(4): Show |
intron_variant | MODIFIER | c.-84-1782_-84-1771d others(14): Show |
RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 2883476 | ||||||
| chr12:2883476 | A | AATATATA others(7): Show |
7 | a0001c0002t0001g0011 a0001c0002t0001g0093 a0001c0002t0001g0121 others(4): Show |
11 | HG01074.hp2 HG01167.hp1 HG02129.hp2 others(8): Show |
intron_variant | MODIFIER | c.-84-1784_-84-1771d others(16): Show |
RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 2883476 | ||||||
| chr12:2883476 | A | AATATATA others(9): Show |
4 | a0001c0002t0001g0033 a0001c0002t0001g0110 a0001c0002t0001g0119 others(1): Show |
5 | HG01070.hp2 HG02056.hp1 HG03942.hp1 others(2): Show |
intron_variant | MODIFIER | c.-84-1786_-84-1771d others(18): Show |
RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 2883476 | ||||||
| chr12:2883476 | A | AATATATA others(11): Show |
4 | a0001c0002t0001g0115 a0001c0002t0001g0116 a0001c0002t0001g0117 others(1): Show |
4 | NA18946.hp2 NA18960.hp1 NA19081.hp1 others(1): Show |
intron_variant | MODIFIER | c.-84-1788_-84-1771d others(20): Show |
RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 2883476 | ||||||
| chr12:2883476 | A | AATATATA others(13): Show |
1 | a0001c0002t0001g0022 | 3 | HG01515.hp2 HG01517.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.-84-1790_-84-1771d others(22): Show |
RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 2883476 | ||||||
| chr12:2883476 | A | AATATATA others(17): Show |
2 | a0001c0002t0001g0114 a0001c0002t0001g0147 |
2 | HG01074.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.-84-1794_-84-1771d others(26): Show |
RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 2883476 | ||||||
| chr12:2883476 | AAT | A | 3 | a0001c0001t0001g0089 a0001c0002t0001g0139 a0001c0002t0001g0140 |
3 | HG01358.hp2 HG02818.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.-84-1772_-84-1771d others(4): Show |
RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 2883476 | ||||||
| chr12:2883478 | T | A | 7 | a0001c0001t0003g0009 a0001c0001t0003g0015 a0001c0001t0003g0020 others(4): Show |
17 | HG01346.hp2 HG02109.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.-84-1805T>A | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | chr12 | 2883478 | |||||||
| chr12:2883489 | ATATATAT others(18): Show |
A | 1 | a0001c0002t0001g0141 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-84-1792_-84-1768d others(27): Show |
RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 2883489 | ||||||
| chr12:2883497 | ATATATAT others(10): Show |
A | 3 | a0001c0002t0001g0001 a0001c0002t0001g0138 a0001c0002t0006g0103 |
3 | HG03471.hp2 NA19072.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.-84-1784_-84-1768d others(19): Show |
RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 2883497 | ||||||
| chr12:2883497 | ATATATAT others(11): Show |
A | 2 | a0001c0001t0002g0004 a0001c0002t0006g0102 |
2 | NA19081.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-84-1784_-84-1767d others(20): Show |
RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 2883497 | ||||||
| chr12:2883497 | ATATATAT others(12): Show |
A | 7 | a0001c0001t0001g0004 a0001c0001t0001g0149 a0001c0001t0002g0004 others(4): Show |
11 | HG01099.hp2 HG02135.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.-84-1784_-84-1766d others(21): Show |
RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 2883497 | ||||||
| chr12:2883499 | ATATATAT others(10): Show |
A | 2 | a0001c0001t0003g0009 a0001c0001t0003g0015 |
2 | HG02818.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-84-1782_-84-1766d others(19): Show |
RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 2883499 | ||||||
| chr12:2883499 | ATATATAT others(11): Show |
A | 3 | a0001c0001t0002g0004 a0001c0001t0002g0024 a0001c0001t0002g0043 |
5 | HG02040.hp1 HG02647.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.-84-1782_-84-1765d others(20): Show |
RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 2883499 | ||||||
| chr12:2883499 | ATATATAT others(12): Show |
A | 14 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0006 others(11): Show |
37 | HG00597.hp1 HG00621.hp1 HG00738.hp2 others(34): Show |
intron_variant | MODIFIER | c.-84-1782_-84-1764d others(21): Show |
RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 2883499 | ||||||
| chr12:2883501 | ATATATAT others(7): Show |
A | 4 | a0001c0001t0001g0002 a0001c0001t0001g0029 a0001c0001t0001g0048 others(1): Show |
4 | NA18971.hp2 NA18999.hp2 NA19058.hp2 others(1): Show |
intron_variant | MODIFIER | c.-84-1780_-84-1767d others(16): Show |
RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 2883501 | ||||||
| chr12:2883501 | ATATATAT others(9): Show |
A | 2 | a0001c0001t0001g0002 a0001c0001t0001g0008 |
4 | HG01106.hp1 HG01952.hp2 HG01975.hp1 others(1): Show |
intron_variant | MODIFIER | c.-84-1780_-84-1765d others(18): Show |
RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 2883501 | ||||||
| chr12:2883501 | ATATATAT others(10): Show |
A | 7 | a0001c0001t0003g0009 a0001c0001t0003g0015 a0001c0001t0003g0020 others(4): Show |
15 | HG01346.hp2 HG02109.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.-84-1780_-84-1764d others(19): Show |
RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 2883501 | ||||||
| chr12:2883501 | ATATATAT others(11): Show |
A | 2 | a0001c0001t0002g0004 a0001c0001t0002g0014 |
3 | HG01943.hp1 HG03704.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.-84-1780_-84-1763d others(20): Show |
RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 2883501 | ||||||
| chr12:2883501 | ATATATAT others(12): Show |
A | 2 | a0001c0001t0002g0004 a0001c0001t0002g0086 |
5 | HG02559.hp2 HG02922.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.-84-1780_-84-1762d others(21): Show |
RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 2883501 | ||||||
| chr12:2883503 | ATATATAT others(5): Show |
A | 1 | a0001c0001t0001g0073 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.-84-1778_-84-1767d others(14): Show |
RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 2883503 | ||||||
| chr12:2883503 | ATATATAT others(6): Show |
A | 1 | a0001c0001t0001g0072 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-84-1778_-84-1766d others(15): Show |
RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 2883503 | ||||||
| chr12:2883503 | ATATATAT others(7): Show |
A | 18 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(15): Show |
45 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(42): Show |
intron_variant | MODIFIER | c.-84-1778_-84-1765d others(16): Show |
RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 2883503 | ||||||
| chr12:2883503 | ATATATAT others(9): Show |
A | 1 | a0001c0001t0002g0004 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-84-1778_-84-1763d others(18): Show |
RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 2883503 | ||||||
| chr12:2883505 | A | T | 1 | a0001c0002t0001g0104 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-84-1778A>T | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | chr12 | 2883505 | |||||||
| chr12:2883505 | ATATATAT others(1): Show |
A | 3 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 |
6 | HG00639.hp1 HG01070.hp1 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.-84-1776_-84-1769d others(10): Show |
RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 2883505 | ||||||
| chr12:2883505 | ATATATAT others(2): Show |
A | 4 | a0001c0001t0001g0003 a0001c0001t0001g0061 a0001c0001t0008g0007 others(1): Show |
6 | HG02080.hp2 NA18939.hp1 NA18956.hp1 others(3): Show |
intron_variant | MODIFIER | c.-84-1776_-84-1768d others(11): Show |
RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 2883505 | ||||||
| chr12:2883505 | ATATATAT others(3): Show |
A | 2 | a0001c0001t0001g0003 a0001c0001t0001g0006 |
2 | NA18950.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-84-1776_-84-1767d others(12): Show |
RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 2883505 | ||||||
| chr12:2883505 | ATATATAT others(5): Show |
A | 4 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0070 others(1): Show |
6 | HG00280.hp1 HG02132.hp2 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.-84-1776_-84-1765d others(14): Show |
RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 2883505 | ||||||
| chr12:2883505 | ATATATAT others(6): Show |
A | 2 | a0001c0001t0001g0002 a0001c0001t0002g0004 |
2 | HG04204.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-84-1776_-84-1764d others(15): Show |
RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 2883505 | ||||||
| chr12:2883505 | ATATATAT others(7): Show |
A | 5 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0027 others(2): Show |
10 | HG00738.hp1 HG01069.hp1 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.-84-1776_-84-1763d others(16): Show |
RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 2883505 | ||||||
| chr12:2883505 | ATATATAT others(8): Show |
A | 1 | a0001c0001t0001g0099 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-84-1776_-84-1762d others(17): Show |
RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 2883505 | ||||||
| chr12:2883505 | ATATATAT others(9): Show |
A | 4 | a0001c0001t0001g0013 a0001c0001t0001g0040 a0001c0001t0001g0041 others(1): Show |
7 | HG01109.hp2 HG01891.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.-84-1776_-84-1761d others(18): Show |
RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 2883505 | ||||||
| chr12:2883507 | A | T | 2 | a0001c0002t0001g0101 a0001c0002t0001g0104 |
2 | HG03579.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-84-1776A>T | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | chr12 | 2883507 | |||||||
| chr12:2883507 | ATATATTT others(1): Show |
A | 5 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(2): Show |
8 | HG00408.hp1 HG01884.hp1 HG02015.hp2 others(5): Show |
intron_variant | MODIFIER | c.-84-1774_-84-1767d others(10): Show |
RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 2883507 | ||||||
| chr12:2883507 | ATATATTT others(3): Show |
A | 1 | a0001c0001t0001g0002 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.-84-1774_-84-1765d others(12): Show |
RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 2883507 | ||||||
| chr12:2883507 | ATATATTT others(5): Show |
A | 2 | a0001c0001t0001g0002 a0001c0001t0001g0006 |
2 | NA18979.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.-84-1774_-84-1763d others(14): Show |
RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 2883507 | ||||||
| chr12:2883507 | ATATATTT others(6): Show |
A | 2 | a0001c0001t0001g0002 a0001c0001t0001g0018 |
2 | HG04115.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.-84-1774_-84-1762d others(15): Show |
RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 2883507 | ||||||
| chr12:2883507 | ATATATTT others(7): Show |
A | 2 | a0001c0001t0001g0002 a0001c0001t0001g0042 |
2 | HG01515.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-84-1774_-84-1761d others(16): Show |
RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 2883507 | ||||||
| chr12:2883509 | A | ATTTTTTT others(8): Show |
2 | a0001c0002t0007g0105 a0001c0002t0007g0106 |
2 | HG03453.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-84-1773_-84-1772i others(17): Show |
RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 2883509 | ||||||
| chr12:2883509 | A | T | 2 | a0001c0002t0001g0101 a0001c0002t0001g0104 |
2 | HG03579.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-84-1774A>T | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | chr12 | 2883509 | |||||||
| chr12:2883509 | ATATTT | A | 5 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0059 others(2): Show |
6 | HG01256.hp1 HG01934.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.-84-1772_-84-1768d others(7): Show |
RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 2883509 | ||||||
| chr12:2883509 | ATATTTT | A | 9 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0028 others(6): Show |
18 | HG00544.hp1 HG00741.hp1 HG01496.hp2 others(15): Show |
intron_variant | MODIFIER | c.-84-1772_-84-1767d others(8): Show |
RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 2883509 | ||||||
| chr12:2883511 | A | ATATATAT others(4): Show |
1 | a0001c0002t0001g0001 | 2 | HG01257.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.-84-1771_-84-1770i others(13): Show |
RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 2883511 | ||||||
| chr12:2883511 | A | ATATATAT others(6): Show |
2 | a0001c0002t0001g0001 a0001c0002t0001g0005 |
2 | HG06807.hp1 NA18942.hp2 |
intron_variant | MODIFIER | c.-84-1771_-84-1770i others(15): Show |
RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 2883511 | ||||||
| chr12:2883511 | A | ATATATAT others(10): Show |
1 | a0001c0002t0001g0001 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.-84-1771_-84-1770i others(19): Show |
RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 2883511 | ||||||
| chr12:2883511 | A | ATATATAT others(12): Show |
1 | a0001c0002t0001g0001 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.-84-1771_-84-1770i others(21): Show |
RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 2883511 | ||||||
| chr12:2883511 | A | ATATATAT others(16): Show |
1 | a0001c0002t0001g0001 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.-84-1771_-84-1770i others(25): Show |
RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 2883511 | ||||||
| chr12:2883511 | A | ATATATAT others(20): Show |
2 | a0001c0002t0001g0001 a0001c0002t0001g0005 |
2 | HG02293.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.-84-1771_-84-1770i others(29): Show |
RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 2883511 | ||||||
| chr12:2883511 | A | ATATATAT others(26): Show |
1 | a0001c0002t0001g0005 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-84-1771_-84-1770i others(35): Show |
RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 2883511 | ||||||
| chr12:2883511 | A | ATATATAT others(18): Show |
1 | a0001c0002t0001g0001 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-84-1771_-84-1770i others(27): Show |
RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 2883511 | ||||||
| chr12:2883511 | A | ATATATAT others(18): Show |
1 | a0001c0002t0001g0001 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-84-1771_-84-1770i others(27): Show |
RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 2883511 | ||||||
| chr12:2883511 | A | ATATATAT others(12): Show |
1 | a0001c0002t0001g0005 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-84-1771_-84-1770i others(21): Show |
RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 2883511 | ||||||
| chr12:2883511 | A | ATATATAT others(9): Show |
3 | a0001c0002t0001g0001 a0001c0002t0001g0005 a0001c0002t0001g0012 |
3 | HG01167.hp2 HG01261.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.-84-1771_-84-1770i others(18): Show |
RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 2883511 | ||||||
| chr12:2883511 | A | ATATATAT others(7): Show |
1 | a0001c0002t0001g0001 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-84-1771_-84-1770i others(16): Show |
RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 2883511 | ||||||
| chr12:2883511 | A | ATATATAT others(8): Show |
1 | a0001c0002t0001g0001 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-84-1771_-84-1770i others(17): Show |
RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 2883511 | ||||||
| chr12:2883511 | A | ATATATAT others(5): Show |
1 | a0001c0002t0001g0001 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.-84-1771_-84-1770i others(14): Show |
RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 2883511 | ||||||
| chr12:2883511 | A | ATATATAT others(4): Show |
1 | a0001c0002t0001g0001 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.-84-1771_-84-1770i others(13): Show |
RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 2883511 | ||||||
| chr12:2883511 | A | ATATATAT others(5): Show |
1 | a0001c0002t0001g0001 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.-84-1771_-84-1770i others(14): Show |
RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 2883511 | ||||||
| chr12:2883511 | A | ATATATTT others(8): Show |
1 | a0003c0005t0016g0107 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-84-1771_-84-1770i others(17): Show |
RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 2883511 | ||||||
| chr12:2883511 | A | T | 4 | a0001c0002t0001g0101 a0001c0002t0001g0104 a0001c0002t0007g0105 others(1): Show |
4 | HG03453.hp2 HG03516.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.-84-1772A>T | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | chr12 | 2883511 | |||||||
| chr12:2883511 | ATTTT | A | 7 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0046 others(4): Show |
9 | HG02647.hp1 NA18957.hp1 NA18966.hp1 others(6): Show |
intron_variant | MODIFIER | c.-84-1752_-84-1749d others(6): Show |
RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 2883511 | ||||||
| chr12:2883511 | ATTTTTTT others(4): Show |
A | 1 | a0001c0001t0001g0003 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.-84-1759_-84-1749d others(13): Show |
RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 2883511 | ||||||
| chr12:2883512 | T | TATATATA | 5 | a0001c0002t0001g0001 a0001c0002t0001g0005 a0001c0002t0001g0012 others(2): Show |
5 | HG01952.hp1 HG02683.hp1 HG04204.hp1 others(2): Show |
intron_variant | MODIFIER | c.-84-1771_-84-1770i others(9): Show |
RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | chr12 | 2883512 | |||||||
| chr12:2883512 | T | TATATATA others(2): Show |
3 | a0001c0002t0001g0001 a0001c0002t0001g0137 a0001c0002t0004g0001 |
8 | HG00423.hp1 HG02965.hp1 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.-84-1771_-84-1770i others(11): Show |
RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | chr12 | 2883512 | |||||||
| chr12:2883512 | T | TATATATA others(4): Show |
4 | a0001c0002t0001g0001 a0001c0002t0001g0021 a0001c0002t0001g0032 others(1): Show |
8 | HG00438.hp1 HG00741.hp2 HG01069.hp2 others(5): Show |
intron_variant | MODIFIER | c.-84-1771_-84-1770i others(13): Show |
RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | chr12 | 2883512 | |||||||
| chr12:2883512 | T | TATATATA others(6): Show |
7 | a0001c0002t0001g0001 a0001c0002t0001g0005 a0001c0002t0001g0044 others(4): Show |
10 | HG00544.hp2 HG02809.hp1 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.-84-1771_-84-1770i others(15): Show |
RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | chr12 | 2883512 | |||||||
| chr12:2883512 | T | TATATATA others(8): Show |
7 | a0001c0002t0001g0001 a0001c0002t0001g0005 a0001c0002t0001g0032 others(4): Show |
13 | HG00639.hp2 HG01081.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.-84-1771_-84-1770i others(17): Show |
RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | chr12 | 2883512 | |||||||
| chr12:2883512 | T | TATATATA others(10): Show |
5 | a0001c0002t0001g0001 a0001c0002t0001g0021 a0001c0002t0001g0133 others(2): Show |
6 | HG00099.hp2 HG01261.hp2 HG01516.hp1 others(3): Show |
intron_variant | MODIFIER | c.-84-1771_-84-1770i others(19): Show |
RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | chr12 | 2883512 | |||||||
| chr12:2883512 | T | TATATATA others(12): Show |
3 | a0001c0002t0001g0001 a0001c0002t0001g0012 a0001c0002t0001g0109 |
6 | HG00597.hp2 HG01516.hp2 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.-84-1771_-84-1770i others(21): Show |
RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | chr12 | 2883512 | |||||||
| chr12:2883512 | T | TATATATA others(14): Show |
1 | a0001c0002t0001g0001 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-84-1771_-84-1770i others(23): Show |
RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | chr12 | 2883512 | |||||||
| chr12:2883512 | T | TATATATA others(16): Show |
2 | a0001c0002t0001g0001 a0001c0002t0001g0113 |
3 | HG02155.hp1 NA18965.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.-84-1771_-84-1770i others(25): Show |
RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | chr12 | 2883512 | |||||||
| chr12:2883512 | T | TATATATA others(20): Show |
1 | a0001c0002t0001g0001 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.-84-1771_-84-1770i others(29): Show |
RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | chr12 | 2883512 | |||||||
| chr12:2883513 | T | A | 25 | a0001c0001t0001g0003 a0001c0002t0001g0001 a0001c0002t0001g0011 others(22): Show |
31 | HG00280.hp2 HG00558.hp2 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.-84-1770T>A | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | chr12 | 2883513 | |||||||
| chr12:2883514 | T | A | 14 | a0001c0001t0001g0007 a0001c0001t0001g0016 a0001c0001t0001g0066 others(11): Show |
31 | HG00544.hp2 HG00597.hp2 HG01069.hp2 others(28): Show |
intron_variant | MODIFIER | c.-84-1769T>A | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | chr12 | 2883514 | |||||||
| chr12:2883515 | T | A | 10 | a0001c0001t0001g0065 a0001c0002t0001g0037 a0001c0002t0001g0108 others(7): Show |
11 | HG00558.hp2 HG00621.hp2 HG00642.hp1 others(8): Show |
intron_variant | MODIFIER | c.-84-1768T>A | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | chr12 | 2883515 | |||||||
| chr12:2883516 | T | A | 4 | a0001c0001t0001g0016 a0001c0001t0001g0066 a0001c0002t0001g0044 others(1): Show |
7 | HG02602.hp1 HG02965.hp2 NA18951.hp2 others(4): Show |
intron_variant | MODIFIER | c.-84-1767T>A | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | chr12 | 2883516 | |||||||
| chr12:2883517 | T | A | 5 | a0001c0001t0001g0094 a0001c0002t0001g0115 a0001c0002t0001g0129 others(2): Show |
5 | HG00558.hp2 HG02647.hp1 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.-84-1766T>A | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | chr12 | 2883517 | |||||||
| chr12:2883518 | T | A | 1 | a0001c0002t0001g0133 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-84-1765T>A | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | chr12 | 2883518 | |||||||
| chr12:2883519 | T | A | 2 | a0001c0001t0010g0097 a0001c0002t0006g0130 |
2 | HG02735.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-84-1764T>A | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | chr12 | 2883519 | |||||||
| chr12:2883520 | T | A | 1 | a0001c0001t0001g0067 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.-84-1763T>A | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | chr12 | 2883520 | |||||||
| chr12:2883521 | T | A | 1 | a0001c0001t0010g0097 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-84-1762T>A | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | chr12 | 2883521 | |||||||
| chr12:2883522 | T | A | 1 | a0001c0001t0001g0067 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.-84-1761T>A | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | chr12 | 2883522 | |||||||
| chr12:2883524 | T | A | 1 | a0001c0001t0001g0067 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.-84-1759T>A | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | chr12 | 2883524 | |||||||
| chr12:2883564 | C | T | 4 | a0001c0001t0001g0013 a0001c0001t0001g0040 a0001c0001t0001g0041 others(1): Show |
7 | HG01109.hp2 HG01891.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.-84-1719C>T | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | chr12 | 2883564 | |||||||
| chr12:2883665 | T | C | 93 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(90): Show |
255 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(252): Show |
intron_variant | MODIFIER | c.-84-1618T>C | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | chr12 | 2883665 | |||||||
| chr12:2883685 | T | C | 2 | a0001c0001t0001g0068 a0001c0001t0001g0069 |
2 | NA18998.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.-84-1598T>C | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | chr12 | 2883685 | |||||||
| chr12:2883717 | C | T | 101 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(98): Show |
264 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(261): Show |
intron_variant | MODIFIER | c.-84-1566C>T | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | chr12 | 2883717 | |||||||
| chr12:2883738 | A | G | 1 | a0001c0001t0001g0088 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-84-1545A>G | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | chr12 | 2883738 | |||||||
| chr12:2883743 | C | T | 1 | a0001c0001t0002g0050 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-84-1540C>T | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | chr12 | 2883743 | |||||||
| chr12:2883759 | A | G | 1 | a0001c0001t0002g0050 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-84-1524A>G | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | chr12 | 2883759 | |||||||
| chr12:2883762 | C | T | 1 | a0001c0001t0002g0050 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-84-1521C>T | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | chr12 | 2883762 | |||||||
| chr12:2883768 | G | A | 1 | a0001c0001t0002g0050 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-84-1515G>A | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | chr12 | 2883768 | |||||||
| chr12:2883773 | T | C | 1 | a0001c0001t0002g0050 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-84-1510T>C | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | chr12 | 2883773 | |||||||
| chr12:2883775 | T | C | 1 | a0001c0001t0002g0050 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-84-1508T>C | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | chr12 | 2883775 | |||||||
| chr12:2883796 | A | G | 1 | a0001c0001t0002g0050 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-84-1487A>G | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | chr12 | 2883796 | |||||||
| chr12:2883798 | G | A | 1 | a0001c0001t0002g0050 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-84-1485G>A | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | chr12 | 2883798 | |||||||
| chr12:2883803 | A | C | 1 | a0001c0001t0002g0050 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-84-1480A>C | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | chr12 | 2883803 | |||||||
| chr12:2883805 | C | T | 92 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(89): Show |
254 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(251): Show |
intron_variant | MODIFIER | c.-84-1478C>T | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | chr12 | 2883805 | |||||||
| chr12:2883806 | G | T | 1 | a0001c0001t0002g0050 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-84-1477G>T | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | chr12 | 2883806 | |||||||
| chr12:2883808 | G | A | 1 | a0001c0001t0002g0050 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-84-1475G>A | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | chr12 | 2883808 | |||||||
| chr12:2883812 | G | A | 1 | a0001c0001t0002g0050 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-84-1471G>A | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | chr12 | 2883812 | |||||||
| chr12:2883813 | GCCAAATA others(393): Show |
G | 1 | a0001c0001t0002g0050 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-84-1466_-84-1067d others(2): Show |
RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 2883813 | ||||||
| chr12:2883891 | C | T | 91 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(88): Show |
253 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(250): Show |
intron_variant | MODIFIER | c.-84-1392C>T | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | chr12 | 2883891 | |||||||
| chr12:2883908 | G | A | 59 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(56): Show |
159 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(156): Show |
intron_variant | MODIFIER | c.-84-1375G>A | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | chr12 | 2883908 | |||||||
| chr12:2883921 | A | G | 2 | a0001c0002t0001g0100 a0001c0002t0001g0101 |
2 | NA19030.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-84-1362A>G | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | chr12 | 2883921 | |||||||
| chr12:2883956 | T | C | 1 | a0001c0002t0001g0001 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.-84-1327T>C | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | chr12 | 2883956 | |||||||
| chr12:2883957 | A | G | 6 | a0001c0002t0001g0001 a0001c0002t0001g0005 a0001c0002t0001g0021 others(3): Show |
21 | HG02074.hp2 HG02155.hp1 HG02523.hp1 others(18): Show |
intron_variant | MODIFIER | c.-84-1326A>G | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | chr12 | 2883957 | |||||||
| chr12:2884072 | T | C | 1 | a0001c0001t0001g0003 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-84-1211T>C | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | chr12 | 2884072 | |||||||
| chr12:2884232 | TTTTGTTT others(1): Show |
T | 3 | a0001c0001t0001g0010 a0001c0001t0001g0095 a0001c0002t0001g0010 |
7 | HG01891.hp2 HG02615.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.-84-1038_-84-1031d others(10): Show |
RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 2884232 | ||||||
| chr12:2884262 | C | T | 1 | a0001c0001t0001g0087 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.-84-1021C>T | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | chr12 | 2884262 | |||||||
| chr12:2884393 | G | A | 101 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(98): Show |
264 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(261): Show |
intron_variant | MODIFIER | c.-84-890G>A | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | chr12 | 2884393 | |||||||
| chr12:2884410 | A | G | 2 | a0001c0002t0001g0100 a0001c0002t0001g0101 |
2 | NA19030.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-84-873A>G | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | chr12 | 2884410 | |||||||
| chr12:2884506 | C | T | 2 | a0001c0002t0006g0102 a0001c0002t0006g0103 |
2 | HG03471.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-84-777C>T | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | chr12 | 2884506 | |||||||
| chr12:2884554 | G | A | 87 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(84): Show |
246 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(243): Show |
intron_variant | MODIFIER | c.-84-729G>A | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | chr12 | 2884554 | |||||||
| chr12:2884628 | G | T | 4 | a0001c0001t0001g0013 a0001c0001t0001g0040 a0001c0001t0001g0041 others(1): Show |
7 | HG01109.hp2 HG01891.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.-84-655G>T | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | chr12 | 2884628 | |||||||
| chr12:2884643 | G | A | 4 | a0001c0002t0007g0105 a0001c0002t0007g0106 a0001c0002t0009g0030 others(1): Show |
5 | HG03098.hp2 HG03453.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.-84-640G>A | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | chr12 | 2884643 | |||||||
| chr12:2884672 | AT | A | 8 | a0001c0001t0001g0013 a0001c0001t0001g0040 a0001c0001t0001g0041 others(5): Show |
11 | HG01109.hp2 HG01891.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.-84-600delT | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr12 | 2884672 | ||||||
| chr12:2884679 | T | A | 1 | a0001c0001t0001g0070 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.-84-604T>A | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | chr12 | 2884679 | |||||||
| chr12:2884792 | G | A | 1 | a0001c0002t0001g0129 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-84-491G>A | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | chr12 | 2884792 | |||||||
| chr12:2884822 | A | G | 1 | a0001c0001t0001g0029 | 2 | NA18984.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.-84-461A>G | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | chr12 | 2884822 | |||||||
| chr12:2884968 | T | C | 93 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(90): Show |
255 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(252): Show |
intron_variant | MODIFIER | c.-84-315T>C | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | chr12 | 2884968 | |||||||
| chr12:2885043 | A | C | 1 | a0001c0001t0002g0086 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-84-240A>C | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | chr12 | 2885043 | |||||||
| chr12:2885170 | G | A | 1 | a0001c0002t0001g0126 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-84-113G>A | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | chr12 | 2885170 | |||||||
| chr12:2885180 | C | T | 1 | a0001c0001t0017g0085 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-84-103C>T | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 1/2 | chr12 | 2885180 | |||||||
| chr12:2885544 | T | C | 3 | a0001c0001t0001g0010 a0001c0001t0001g0095 a0001c0002t0001g0010 |
7 | HG01891.hp2 HG02615.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.168+10T>C | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 2/2 | chr12 | 2885544 | |||||||
| chr12:2885560 | C | CTTTTTTT others(4): Show |
1 | a0001c0002t0001g0101 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.168+26_168+27insTT others(9): Show |
RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 2/2 | chr12 | 2885560 | |||||||
| chr12:2885560 | CAT | C | 2 | a0001c0002t0009g0030 a0003c0005t0016g0107 |
3 | HG03098.hp2 HG06807.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.168+27_168+28delAT | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 2/2 | chr12 | 2885560 | |||||||
| chr12:2885560 | CATTTTT | C | 7 | a0001c0001t0001g0007 a0001c0001t0001g0041 a0001c0001t0001g0046 others(4): Show |
14 | HG00741.hp1 HG01496.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.168+27_168+32delAT others(4): Show |
RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 2/2 | chr12 | 2885560 | |||||||
| chr12:2885560 | CATTTTTT | C | 31 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(28): Show |
75 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.168+27_168+33delAT others(5): Show |
RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 2/2 | chr12 | 2885560 | |||||||
| chr12:2885560 | CATTTTTT others(1): Show |
C | 26 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0010 others(23): Show |
76 | HG00597.hp1 HG00621.hp1 HG00639.hp1 others(73): Show |
intron_variant | MODIFIER | c.168+27_168+34delAT others(6): Show |
RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 2/2 | chr12 | 2885560 | |||||||
| chr12:2885560 | CATTTTTT others(2): Show |
C | 29 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0018 others(26): Show |
87 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.168+27_168+35delAT others(7): Show |
RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 2/2 | chr12 | 2885560 | |||||||
| chr12:2885560 | CATTTTTT others(3): Show |
C | 2 | a0001c0001t0001g0017 a0001c0001t0003g0062 |
5 | HG02895.hp1 HG03017.hp2 HG03834.hp2 others(2): Show |
intron_variant | MODIFIER | c.168+27_168+36delAT others(8): Show |
RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 2/2 | chr12 | 2885560 | |||||||
| chr12:2885561 | A | AT | 22 | a0001c0002t0001g0001 a0001c0002t0001g0005 a0001c0002t0001g0021 others(19): Show |
46 | HG00423.hp1 HG00438.hp1 HG00642.hp1 others(43): Show |
intron_variant | MODIFIER | c.168+58dupT | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 2885561 | ||||||
| chr12:2885561 | A | ATT | 6 | a0001c0002t0001g0001 a0001c0002t0001g0011 a0001c0002t0001g0038 others(3): Show |
8 | HG01192.hp1 HG02559.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.168+57_168+58dupTT | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 2885561 | ||||||
| chr12:2885561 | A | T | 3 | a0001c0002t0001g0001 a0001c0002t0001g0100 a0001c0002t0001g0101 |
3 | HG01943.hp2 NA19030.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.168+27A>T | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 2/2 | chr12 | 2885561 | |||||||
| chr12:2885570 | T | C | 1 | a0001c0001t0002g0071 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.168+36T>C | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 2/2 | chr12 | 2885570 | |||||||
| chr12:2885591 | T | A | 1 | a0001c0002t0001g0134 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.168+57T>A | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 2/2 | chr12 | 2885591 | |||||||
| chr12:2885614 | G | A | 1 | a0001c0001t0001g0090 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.168+80G>A | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 2/2 | chr12 | 2885614 | |||||||
| chr12:2885636 | G | A | 7 | a0001c0001t0003g0009 a0001c0001t0003g0015 a0001c0001t0003g0020 others(4): Show |
17 | HG01346.hp2 HG02109.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.168+102G>A | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 2/2 | chr12 | 2885636 | |||||||
| chr12:2885765 | T | C | 93 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(90): Show |
255 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(252): Show |
intron_variant | MODIFIER | c.168+231T>C | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 2/2 | chr12 | 2885765 | |||||||
| chr12:2885777 | G | A | 93 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(90): Show |
255 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(252): Show |
intron_variant | MODIFIER | c.168+243G>A | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 2/2 | chr12 | 2885777 | |||||||
| chr12:2885811 | G | A | 93 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(90): Show |
255 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(252): Show |
intron_variant | MODIFIER | c.168+277G>A | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 2/2 | chr12 | 2885811 | |||||||
| chr12:2885818 | G | T | 93 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(90): Show |
255 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(252): Show |
intron_variant | MODIFIER | c.168+284G>T | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 2/2 | chr12 | 2885818 | |||||||
| chr12:2885822 | G | A | 1 | a0001c0001t0001g0072 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.168+288G>A | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 2/2 | chr12 | 2885822 | |||||||
| chr12:2885826 | C | T | 1 | a0001c0002t0001g0119 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.168+292C>T | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 2/2 | chr12 | 2885826 | |||||||
| chr12:2885866 | CGCCCGGC others(48): Show |
C | 93 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(90): Show |
255 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(252): Show |
intron_variant | MODIFIER | c.168+392_168+446del others(55): Show |
RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 2885866 | ||||||
| chr12:2885980 | C | T | 2 | a0001c0002t0001g0100 a0001c0002t0001g0101 |
2 | NA19030.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.168+446C>T | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 2/2 | chr12 | 2885980 | |||||||
| chr12:2886022 | G | C | 93 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(90): Show |
255 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(252): Show |
intron_variant | MODIFIER | c.168+488G>C | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 2/2 | chr12 | 2886022 | |||||||
| chr12:2886087 | T | G | 4 | a0001c0002t0001g0116 a0001c0002t0001g0122 a0001c0002t0001g0131 others(1): Show |
4 | HG00558.hp2 NA18946.hp1 NA19067.hp1 others(1): Show |
intron_variant | MODIFIER | c.168+553T>G | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 2/2 | chr12 | 2886087 | |||||||
| chr12:2886101 | C | T | 3 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0076 |
3 | HG00735.hp2 HG01928.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.168+567C>T | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 2/2 | chr12 | 2886101 | |||||||
| chr12:2886157 | T | A | 1 | a0001c0001t0001g0099 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.168+623T>A | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 2/2 | chr12 | 2886157 | |||||||
| chr12:2886157 | T | G | 92 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(89): Show |
254 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(251): Show |
intron_variant | MODIFIER | c.168+623T>G | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 2/2 | chr12 | 2886157 | |||||||
| chr12:2886415 | C | G | 1 | a0001c0001t0001g0073 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.168+881C>G | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 2/2 | chr12 | 2886415 | |||||||
| chr12:2886580 | C | T | 1 | a0001c0001t0001g0149 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.168+1046C>T | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 2/2 | chr12 | 2886580 | |||||||
| chr12:2886655 | C | CA | 12 | a0001c0002t0001g0005 a0001c0002t0001g0098 a0001c0002t0001g0111 others(9): Show |
22 | HG00558.hp2 HG00639.hp2 HG00642.hp1 others(19): Show |
intron_variant | MODIFIER | c.168+1143dupA | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 2886655 | ||||||
| chr12:2886655 | CA | C | 21 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0046 others(18): Show |
32 | HG01106.hp1 HG01891.hp2 HG01934.hp1 others(29): Show |
intron_variant | MODIFIER | c.168+1143delA | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 2886655 | ||||||
| chr12:2886655 | CAA | C | 67 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(64): Show |
217 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(214): Show |
intron_variant | MODIFIER | c.168+1142_168+1143d others(4): Show |
RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 2886655 | ||||||
| chr12:2886655 | CAAA | C | 10 | a0001c0001t0001g0027 a0001c0001t0001g0040 a0001c0001t0001g0076 others(7): Show |
11 | HG01069.hp1 HG01975.hp2 HG01993.hp2 others(8): Show |
intron_variant | MODIFIER | c.168+1141_168+1143d others(5): Show |
RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 2886655 | ||||||
| chr12:2886667 | A | G | 1 | a0001c0001t0017g0085 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.168+1133A>G | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 2/2 | chr12 | 2886667 | |||||||
| chr12:2886899 | T | C | 1 | a0001c0001t0001g0074 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.169-1012T>C | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 2/2 | chr12 | 2886899 | |||||||
| chr12:2887008 | A | G | 87 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(84): Show |
246 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(243): Show |
intron_variant | MODIFIER | c.169-903A>G | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 2/2 | chr12 | 2887008 | |||||||
| chr12:2887011 | A | G | 1 | a0001c0002t0001g0101 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.169-900A>G | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 2/2 | chr12 | 2887011 | |||||||
| chr12:2887045 | A | G | 93 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(90): Show |
255 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(252): Show |
intron_variant | MODIFIER | c.169-866A>G | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 2/2 | chr12 | 2887045 | |||||||
| chr12:2887126 | T | G | 1 | a0001c0001t0002g0057 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.169-785T>G | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 2/2 | chr12 | 2887126 | |||||||
| chr12:2887138 | T | G | 1 | a0001c0001t0002g0057 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.169-773T>G | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 2/2 | chr12 | 2887138 | |||||||
| chr12:2887143 | G | A | 1 | a0001c0001t0002g0057 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.169-768G>A | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 2/2 | chr12 | 2887143 | |||||||
| chr12:2887144 | A | G | 1 | a0001c0001t0002g0057 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.169-767A>G | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 2/2 | chr12 | 2887144 | |||||||
| chr12:2887145 | C | A | 1 | a0001c0001t0002g0057 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.169-766C>A | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 2/2 | chr12 | 2887145 | |||||||
| chr12:2887150 | C | A | 1 | a0001c0001t0002g0057 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.169-761C>A | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 2/2 | chr12 | 2887150 | |||||||
| chr12:2887154 | C | A | 1 | a0001c0001t0002g0057 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.169-757C>A | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 2/2 | chr12 | 2887154 | |||||||
| chr12:2887156 | A | T | 1 | a0001c0001t0002g0057 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.169-755A>T | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 2/2 | chr12 | 2887156 | |||||||
| chr12:2887158 | C | A | 1 | a0001c0001t0002g0057 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.169-753C>A | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 2/2 | chr12 | 2887158 | |||||||
| chr12:2887159 | A | T | 1 | a0001c0001t0002g0057 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.169-752A>T | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 2/2 | chr12 | 2887159 | |||||||
| chr12:2887160 | C | A | 1 | a0001c0001t0002g0057 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.169-751C>A | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 2/2 | chr12 | 2887160 | |||||||
| chr12:2887170 | C | CT | 4 | a0001c0002t0007g0105 a0001c0002t0007g0106 a0001c0002t0009g0030 others(1): Show |
5 | HG03098.hp2 HG03453.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.169-740dupT | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 2887170 | ||||||
| chr12:2887170 | C | T | 1 | a0001c0001t0002g0057 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.169-741C>T | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 2/2 | chr12 | 2887170 | |||||||
| chr12:2887172 | G | A | 1 | a0001c0001t0002g0057 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.169-739G>A | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 2/2 | chr12 | 2887172 | |||||||
| chr12:2887176 | C | A | 1 | a0001c0001t0002g0057 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.169-735C>A | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 2/2 | chr12 | 2887176 | |||||||
| chr12:2887179 | T | G | 1 | a0001c0001t0002g0057 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.169-732T>G | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 2/2 | chr12 | 2887179 | |||||||
| chr12:2887181 | A | G | 1 | a0001c0001t0002g0057 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.169-730A>G | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 2/2 | chr12 | 2887181 | |||||||
| chr12:2887182 | A | T | 1 | a0001c0001t0002g0057 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.169-729A>T | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 2/2 | chr12 | 2887182 | |||||||
| chr12:2887183 | A | T | 1 | a0001c0001t0002g0057 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.169-728A>T | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 2/2 | chr12 | 2887183 | |||||||
| chr12:2887184 | A | T | 1 | a0001c0001t0002g0057 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.169-727A>T | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 2/2 | chr12 | 2887184 | |||||||
| chr12:2887185 | A | T | 1 | a0001c0001t0002g0057 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.169-726A>T | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 2/2 | chr12 | 2887185 | |||||||
| chr12:2887187 | A | G | 1 | a0001c0001t0002g0057 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.169-724A>G | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 2/2 | chr12 | 2887187 | |||||||
| chr12:2887189 | A | T | 1 | a0001c0001t0002g0057 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.169-722A>T | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 2/2 | chr12 | 2887189 | |||||||
| chr12:2887190 | A | T | 1 | a0001c0001t0002g0057 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.169-721A>T | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 2/2 | chr12 | 2887190 | |||||||
| chr12:2887191 | A | T | 1 | a0001c0001t0002g0057 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.169-720A>T | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 2/2 | chr12 | 2887191 | |||||||
| chr12:2887192 | A | T | 1 | a0001c0001t0002g0057 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.169-719A>T | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 2/2 | chr12 | 2887192 | |||||||
| chr12:2887193 | A | T | 1 | a0001c0001t0002g0057 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.169-718A>T | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 2/2 | chr12 | 2887193 | |||||||
| chr12:2887198 | C | G | 1 | a0001c0001t0002g0057 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.169-713C>G | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 2/2 | chr12 | 2887198 | |||||||
| chr12:2887199 | T | A | 1 | a0001c0001t0002g0057 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.169-712T>A | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 2/2 | chr12 | 2887199 | |||||||
| chr12:2887205 | C | A | 1 | a0001c0001t0002g0057 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.169-706C>A | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 2/2 | chr12 | 2887205 | |||||||
| chr12:2887207 | G | A | 2 | a0001c0002t0006g0102 a0001c0002t0006g0103 |
2 | HG03471.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.169-704G>A | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 2/2 | chr12 | 2887207 | |||||||
| chr12:2887211 | C | A | 1 | a0001c0001t0002g0057 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.169-700C>A | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 2/2 | chr12 | 2887211 | |||||||
| chr12:2887235 | T | C | 1 | a0001c0002t0001g0144 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.169-676T>C | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 2/2 | chr12 | 2887235 | |||||||
| chr12:2887273 | T | A | 2 | a0001c0001t0001g0010 a0001c0002t0001g0010 |
6 | HG01891.hp2 HG02615.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.169-638T>A | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 2/2 | chr12 | 2887273 | |||||||
| chr12:2887352 | C | T | 2 | a0001c0001t0001g0080 a0001c0001t0015g0081 |
2 | HG00408.hp2 HG02080.hp1 |
intron_variant | MODIFIER | c.169-559C>T | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 2/2 | chr12 | 2887352 | |||||||
| chr12:2887383 | C | T | 2 | a0001c0002t0006g0102 a0001c0002t0006g0103 |
2 | HG03471.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.169-528C>T | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 2/2 | chr12 | 2887383 | |||||||
| chr12:2887432 | C | G | 101 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(98): Show |
264 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(261): Show |
intron_variant | MODIFIER | c.169-479C>G | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 2/2 | chr12 | 2887432 | |||||||
| chr12:2887478 | C | CA | 16 | a0001c0001t0001g0066 a0001c0001t0010g0097 a0001c0002t0001g0012 others(13): Show |
20 | HG00741.hp2 HG01261.hp1 HG01346.hp1 others(17): Show |
intron_variant | MODIFIER | c.169-411dupA | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 2887478 | ||||||
| chr12:2887478 | CA | C | 81 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(78): Show |
237 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(234): Show |
intron_variant | MODIFIER | c.169-411delA | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 2887478 | ||||||
| chr12:2887478 | CAA | C | 6 | a0001c0001t0001g0013 a0001c0001t0001g0041 a0001c0001t0001g0042 others(3): Show |
10 | HG01109.hp2 HG01891.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.169-412_169-411del others(2): Show |
RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 2887478 | ||||||
| chr12:2887509 | C | T | 4 | a0001c0002t0007g0105 a0001c0002t0007g0106 a0001c0002t0009g0030 others(1): Show |
5 | HG03098.hp2 HG03453.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.169-402C>T | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 2/2 | chr12 | 2887509 | |||||||
| chr12:2887526 | G | T | 1 | a0001c0002t0001g0143 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.169-385G>T | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 2/2 | chr12 | 2887526 | |||||||
| chr12:2887804 | T | C | 1 | a0001c0001t0001g0149 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.169-107T>C | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 2/2 | chr12 | 2887804 | |||||||
| chr12:2887892 | CT | C | 8 | a0001c0001t0001g0026 a0001c0001t0001g0082 a0001c0001t0012g0055 others(5): Show |
9 | HG01168.hp2 HG02965.hp1 HG03471.hp2 others(6): Show |
splice_region_variant&intron_variant | LOW | c.169-4delT | RHNO1 | ENSG00000171792.11 | transcript | ENST00000489288.7 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr12 | 2887892 |