Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 54870 |
| ensemblid | ENSG00000198218.12 |
| hgncid | 24713 |
| symbol | QRICH1 |
| name | glutamine rich 1 |
| refseq_nuc | NM_198880.3 |
| refseq_prot | NP_942581.1 |
| ensembl_nuc | ENST00000395443.7 |
| ensembl_prot | ENSP00000378830.2 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 49029707 |
| end | 49094071 |
| strand | - |
| ver | v1.2 |
| region | chr3:49029707-49094071 |
| region5000 | chr3:49024707-49099071 |
| regionname0 | QRICH1_chr3_49029707_49094071 |
| regionname5000 | QRICH1_chr3_49024707_49099071 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 776 | 206 | 78 | 40 | 51 | 11 | 24 | 34 | QRICH1_chr3_49024707_49099071 | QRICH1 | MNNSL others(771): Show |
chr3 | 49024707 | 49099071 |
| a0002 | 0/0 | 776 | 20 | 0 | 6 | 9 | 3 | 2 | 6 | QRICH1_chr3_49024707_49099071 | QRICH1 | MNNSL others(771): Show |
chr3 | 49024707 | 49099071 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2328 | 204 | 77 | 40 | 50 | 11 | 24 | QRICH1_chr3_49024707_49099071 | QRICH1 | ATGAA others(2323): Show |
chr3 | 49024707 | 49099071 | ||
| a0001c0003 | 0/0 | 2328 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | ATGAA others(2323): Show |
chr3 | 49024707 | 49099071 | ||
| a0001c0004 | 0/0 | 2328 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | ATGAA others(2323): Show |
chr3 | 49024707 | 49099071 | ||
| a0002c0002 | 0/0 | 2328 | 20 | 0 | 6 | 9 | 3 | 2 | QRICH1_chr3_49024707_49099071 | QRICH1 | ATGAA others(2323): Show |
chr3 | 49024707 | 49099071 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 3257 | 193 | 72 | 38 | 48 | 11 | 23 | QRICH1_chr3_49024707_49099071 | QRICH1 | ATTGG others(3252): Show |
chr3 | 49024707 | 49099071 |
| a0001c0001t0002 | 0/0 | 3258 | 4 | 3 | 1 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | ATTGG others(3253): Show |
chr3 | 49024707 | 49099071 |
| a0001c0001t0003 | 0/0 | 3260 | 2 | 2 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | ATTGG others(3255): Show |
chr3 | 49024707 | 49099071 |
| a0001c0001t0005 | 0/0 | 3257 | 1 | 0 | 0 | 0 | 0 | 1 | QRICH1_chr3_49024707_49099071 | QRICH1 | ATTGG others(3252): Show |
chr3 | 49024707 | 49099071 |
| a0001c0001t0006 | 0/0 | 3257 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | ATTGG others(3252): Show |
chr3 | 49024707 | 49099071 |
| a0001c0001t0007 | 0/0 | 3257 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | ATTGG others(3252): Show |
chr3 | 49024707 | 49099071 |
| a0001c0001t0008 | 0/1 | 3258 | 1 | 0 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | ATTGG others(3253): Show |
chr3 | 49024707 | 49099071 |
| a0001c0001t0009 | 0/0 | 3257 | 1 | 0 | 1 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | ATTGG others(3252): Show |
chr3 | 49024707 | 49099071 |
| a0001c0003t0001 | 0/0 | 3257 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | ATTGG others(3252): Show |
chr3 | 49024707 | 49099071 |
| a0001c0004t0002 | 0/0 | 3258 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | ATTGG others(3253): Show |
chr3 | 49024707 | 49099071 |
| a0002c0002t0001 | 0/0 | 3257 | 16 | 0 | 6 | 5 | 3 | 2 | QRICH1_chr3_49024707_49099071 | QRICH1 | ATTGG others(3252): Show |
chr3 | 49024707 | 49099071 |
| a0002c0002t0003 | 0/0 | 3260 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | ATTGG others(3255): Show |
chr3 | 49024707 | 49099071 |
| a0002c0002t0004 | 0/0 | 3257 | 3 | 0 | 0 | 3 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | ATTGG others(3252): Show |
chr3 | 49024707 | 49099071 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0020 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0002g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0003g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0003g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0005g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0006g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0007g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0008g0089 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0001t0009g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0003t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0001c0004t0002g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0002c0002t0001g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0002c0002t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0002c0002t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0002c0002t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0002c0002t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0002c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0002c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0002c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0002c0002t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0002c0002t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0002c0002t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0002c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0002c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0002c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0002c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0002c0002t0003g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0002c0002t0004g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0002c0002t0004g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| a0002c0002t0004g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0022 | EUR | GBR | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0210 | EUR | GBR | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0025 | EUR | FIN | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0212 | EUR | FIN | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | CHS | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | CHS | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | CHS | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG00609 | hp2 | a0002 | c0002 | t0001 | g0063 | EAS | CHS | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG00639 | hp1 | a0002 | c0002 | t0001 | g0046 | AMR | PUR | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG00733 | hp2 | a0002 | c0002 | t0001 | g0041 | AMR | PUR | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG00735 | hp1 | a0001 | c0001 | t0009 | g0222 | AMR | PUR | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG00735 | hp2 | a0002 | c0002 | t0001 | g0045 | AMR | PUR | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | PUR | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | PUR | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG01070 | hp1 | a0002 | c0002 | t0001 | g0047 | AMR | PUR | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG01071 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0169 | AMR | PUR | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0142 | AMR | PUR | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0197 | AMR | PUR | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG01099 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0066 | AMR | PUR | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | PUR | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | PUR | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0190 | AMR | PUR | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | CLM | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | CLM | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | CLM | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0068 | AMR | CLM | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0166 | AMR | CLM | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | CLM | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | CLM | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0209 | AMR | CLM | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0182 | AMR | CLM | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | CLM | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | CLM | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0095 | AMR | CLM | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG01515 | hp1 | a0002 | c0002 | t0001 | g0039 | EUR | IBS | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0028 | EUR | IBS | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0213 | EUR | IBS | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0013 | EUR | IBS | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0030 | EUR | IBS | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG01517 | hp2 | a0002 | c0002 | t0001 | g0048 | EUR | IBS | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | ACB | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | PEL | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0101 | AMR | PEL | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | PEL | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | PEL | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0163 | AMR | PEL | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0090 | AMR | PEL | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | PEL | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | PEL | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | KHV | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | KHV | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG02071 | hp1 | a0002 | c0002 | t0003 | g0220 | EAS | KHV | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | KHV | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | KHV | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | KHV | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | KHV | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | KHV | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | KHV | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | KHV | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | KHV | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | KHV | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | ACB | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0216 | AFR | ACB | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | ACB | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | ACB | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | ACB | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | PEL | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | ACB | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | ACB | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0207 | AFR | GWD | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | GWD | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0215 | SAS | PJL | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0158 | SAS | PJL | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | GWD | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | GWD | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | GWD | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | GWD | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | GWD | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0204 | AFR | GWD | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0037 | AFR | GWD | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG02723 | hp2 | a0001 | c0001 | t0003 | g0219 | AFR | GWD | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0059 | SAS | PJL | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0050 | SAS | PJL | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | GWD | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | GWD | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | GWD | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | GWD | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0199 | AFR | GWD | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0193 | AFR | ESN | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | ESN | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | ESN | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | ESN | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | ESN | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | ESN | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0208 | SAS | PJL | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0183 | SAS | PJL | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0218 | AFR | GWD | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | GWD | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | MSL | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | MSL | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | ESN | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0077 | AFR | ESN | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0195 | AFR | ESN | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0184 | AFR | ESN | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0196 | AFR | MSL | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | MSL | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0100 | SAS | PJL | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0217 | AFR | MSL | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | MSL | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0176 | SAS | PJL | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0186 | SAS | PJL | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0185 | SAS | PJL | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0136 | SAS | PJL | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG03516 | hp1 | a0001 | c0001 | t0003 | g0221 | AFR | ESN | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0206 | AFR | ESN | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0201 | AFR | GWD | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | GWD | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0202 | AFR | MSL | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | MSL | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0027 | SAS | STU | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0128 | SAS | STU | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0102 | SAS | PJL | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0115 | SAS | PJL | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0214 | SAS | BEB | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG03831 | hp2 | a0002 | c0002 | t0001 | g0058 | SAS | BEB | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG03834 | hp1 | a0002 | c0002 | t0001 | g0042 | SAS | BEB | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | BEB | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0108 | SAS | BEB | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0211 | SAS | BEB | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0164 | SAS | STU | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0162 | SAS | STU | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0177 | SAS | BEB | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG04184 | hp2 | a0001 | c0001 | t0005 | g0138 | SAS | BEB | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | YRI | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0200 | AFR | YRI | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | CHB | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| NA18612 | hp2 | a0001 | c0001 | t0006 | g0120 | EAS | CHB | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | CHB | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| NA18747 | hp2 | a0002 | c0002 | t0001 | g0044 | EAS | CHB | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | YRI | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | YRI | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| NA18954 | hp1 | a0002 | c0002 | t0004 | g0224 | EAS | JPT | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| NA18962 | hp1 | a0001 | c0001 | t0007 | g0134 | EAS | JPT | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| NA18973 | hp1 | a0002 | c0002 | t0001 | g0040 | EAS | JPT | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| NA18979 | hp1 | a0002 | c0002 | t0001 | g0064 | EAS | JPT | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | LWK | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | LWK | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | LWK | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | LWK | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| NA19057 | hp1 | a0001 | c0003 | t0001 | g0094 | EAS | JPT | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| NA19057 | hp2 | a0002 | c0002 | t0004 | g0225 | EAS | JPT | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| NA19080 | hp1 | a0002 | c0002 | t0004 | g0223 | EAS | JPT | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| NA19089 | hp1 | a0002 | c0002 | t0001 | g0011 | EAS | JPT | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | YRI | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | YRI | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | ASW | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | ASW | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0019 | EUR | TSI | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| NA20752 | hp2 | a0002 | c0002 | t0001 | g0043 | EUR | TSI | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0161 | EUR | TSI | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0029 | EUR | TSI | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | ACB | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | ACB | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0205 | AFR | ACB | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | ACB | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | ACB | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | MSL | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0198 | AFR | MSL | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | USA | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| HG06807 | hp2 | a0001 | c0004 | t0002 | g0003 | AFR | USA | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | USA | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | USA | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | LWK | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | LWK | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0008 | g0089 | REF | REF | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0020 | REF | REF | QRICH1_chr3_49024707_49099071 | QRICH1 | chr3 | 49024707 | 49099071 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:49030471 | T | C | 1 | a0002 | 20 | HG00609.hp2 HG00639.hp1 HG00733.hp2 others(17): Show |
missense_variant | MODERATE | c.2312A>G | p.Asn771Ser | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 10/10 | 2493/3257 | 2312/2331 | 771/776 | chr3 | 49030471 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:49057471 | T | C | 1 | a0001c0004 | 1 | HG06807.hp2 | synonymous_variant | LOW | c.729A>G | p.Gln243Gln | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/10 | 910/3257 | 729/2331 | 243/776 | chr3 | 49057471 | |||
| chr3:49057714 | C | T | 1 | a0001c0003 | 1 | NA19057.hp1 | synonymous_variant | LOW | c.486G>A | p.Ser162Ser | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/10 | 667/3257 | 486/2331 | 162/776 | chr3 | 49057714 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:49029862 | C | CA | 2 | a0001c0001t0002 a0001c0004t0002 |
5 | HG01981.hp1 HG02723.hp1 HG03041.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*589dupT | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 10/10 | 589 | chr3 | 49029862 | ||||||
| chr3:49029969 | C | A | 1 | a0001c0001t0006 | 1 | NA18612.hp2 | 3_prime_UTR_variant | MODIFIER | c.*483G>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 10/10 | 483 | chr3 | 49029969 | ||||||
| chr3:49030186 | C | G | 1 | a0001c0001t0005 | 1 | HG04184.hp2 | 3_prime_UTR_variant | MODIFIER | c.*266G>C | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 10/10 | 266 | chr3 | 49030186 | ||||||
| chr3:49030332 | G | A | 1 | a0001c0001t0007 | 1 | NA18962.hp1 | 3_prime_UTR_variant | MODIFIER | c.*120C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 10/10 | 120 | chr3 | 49030332 | ||||||
| chr3:49093925 | T | TGCC | 2 | a0001c0001t0003 a0002c0002t0003 |
3 | HG02071.hp1 HG02723.hp2 HG03516.hp1 |
5_prime_UTR_variant | MODIFIER | c.-38_-36dupGGC | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/10 | 16909 | chr3 | 49093925 | ||||||
| chr3:49093941 | G | A | 1 | a0001c0001t0009 | 1 | HG00735.hp1 | 5_prime_UTR_variant | MODIFIER | c.-51C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/10 | 16924 | chr3 | 49093941 | ||||||
| chr3:49094007 | G | C | 1 | a0002c0002t0004 | 3 | NA18954.hp1 NA19057.hp2 NA19080.hp1 |
5_prime_UTR_variant | MODIFIER | c.-117C>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/10 | 16990 | chr3 | 49094007 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:49030794 | A | G | 1 | a0001c0001t0001g0143 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.2139-150T>C | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 9/9 | chr3 | 49030794 | |||||||
| chr3:49030898 | C | T | 5 | a0001c0001t0001g0002 a0001c0001t0001g0033 a0001c0001t0001g0034 others(2): Show |
5 | HG02145.hp1 HG02257.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.2139-254G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 9/9 | chr3 | 49030898 | |||||||
| chr3:49030991 | C | CT | 9 | a0001c0001t0001g0025 a0001c0001t0001g0062 a0001c0001t0001g0108 others(6): Show |
9 | HG00280.hp1 HG01074.hp1 HG02074.hp1 others(6): Show |
intron_variant | MODIFIER | c.2139-348dupA | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 9/9 | chr3 | 49030991 | |||||||
| chr3:49031351 | C | T | 3 | a0001c0001t0002g0004 a0001c0001t0002g0218 a0001c0004t0002g0003 |
3 | HG03041.hp1 HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.2139-707G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 9/9 | chr3 | 49031351 | |||||||
| chr3:49031503 | T | C | 2 | a0001c0001t0001g0109 a0001c0001t0001g0126 |
2 | HG01168.hp2 HG01256.hp1 |
intron_variant | MODIFIER | c.2138+680A>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 9/9 | chr3 | 49031503 | |||||||
| chr3:49031677 | A | C | 3 | a0001c0001t0002g0004 a0001c0001t0002g0218 a0001c0004t0002g0003 |
3 | HG03041.hp1 HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.2138+506T>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 9/9 | chr3 | 49031677 | |||||||
| chr3:49032529 | C | G | 4 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(1): Show |
4 | HG02145.hp1 HG02257.hp1 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.2047+93G>C | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 8/9 | chr3 | 49032529 | |||||||
| chr3:49032960 | T | C | 1 | a0001c0001t0001g0170 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1895+160A>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 7/9 | chr3 | 49032960 | |||||||
| chr3:49033066 | C | T | 201 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(198): Show |
202 | HG00140.hp2 HG00280.hp2 HG00544.hp1 others(199): Show |
intron_variant | MODIFIER | c.1895+54G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 7/9 | chr3 | 49033066 | |||||||
| chr3:49033339 | G | T | 3 | a0001c0001t0002g0004 a0001c0001t0002g0218 a0001c0004t0002g0003 |
3 | HG03041.hp1 HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1787-111C>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49033339 | |||||||
| chr3:49033405 | C | T | 1 | a0001c0001t0001g0036 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1787-177G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49033405 | |||||||
| chr3:49033420 | G | A | 1 | a0001c0001t0001g0114 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1787-192C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49033420 | |||||||
| chr3:49033816 | G | A | 2 | a0001c0001t0001g0091 a0001c0001t0001g0184 |
2 | HG02280.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1787-588C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49033816 | |||||||
| chr3:49033855 | C | T | 1 | a0001c0001t0001g0080 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1787-627G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49033855 | |||||||
| chr3:49033936 | G | A | 2 | a0001c0001t0002g0004 a0001c0004t0002g0003 |
2 | HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1787-708C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49033936 | |||||||
| chr3:49033963 | GGCAACAG others(1): Show |
G | 17 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0001t0001g0107 others(14): Show |
17 | HG00140.hp2 HG00280.hp2 HG00738.hp2 others(14): Show |
intron_variant | MODIFIER | c.1787-743_1787-736d others(10): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49033963 | |||||||
| chr3:49033974 | G | C | 17 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0001t0001g0107 others(14): Show |
17 | HG00140.hp2 HG00280.hp2 HG00738.hp2 others(14): Show |
intron_variant | MODIFIER | c.1787-746C>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49033974 | |||||||
| chr3:49034017 | A | C | 10 | a0001c0001t0001g0079 a0002c0002t0001g0001 a0002c0002t0001g0039 others(7): Show |
11 | HG00639.hp1 HG00733.hp2 HG00735.hp2 others(8): Show |
intron_variant | MODIFIER | c.1787-789T>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49034017 | |||||||
| chr3:49034079 | T | TATTATTA others(6): Show |
1 | a0001c0001t0001g0153 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1787-852_1787-851i others(15): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49034079 | |||||||
| chr3:49034079 | T | TTTA | 127 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(124): Show |
127 | HG00140.hp2 HG00280.hp2 HG00544.hp1 others(124): Show |
intron_variant | MODIFIER | c.1787-854_1787-852d others(5): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49034079 | |||||||
| chr3:49034079 | T | TTTATTA | 16 | a0001c0001t0001g0008 a0001c0001t0001g0083 a0001c0001t0001g0092 others(13): Show |
16 | HG01071.hp2 HG02109.hp1 HG02559.hp2 others(13): Show |
intron_variant | MODIFIER | c.1787-857_1787-852d others(8): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49034079 | |||||||
| chr3:49034079 | T | TTTATTAT others(2): Show |
9 | a0001c0001t0001g0007 a0001c0001t0001g0060 a0001c0001t0001g0071 others(6): Show |
9 | HG00735.hp1 HG02145.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.1787-860_1787-852d others(11): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49034079 | |||||||
| chr3:49034079 | T | TTTATTAT others(5): Show |
4 | a0001c0001t0001g0088 a0001c0001t0001g0090 a0001c0001t0001g0096 others(1): Show |
4 | HG01981.hp2 HG02818.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1787-863_1787-852d others(14): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49034079 | |||||||
| chr3:49034079 | T | TTTATTAT others(8): Show |
4 | a0001c0001t0001g0006 a0001c0001t0001g0033 a0001c0001t0001g0034 others(1): Show |
4 | HG01884.hp2 HG02257.hp1 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.1787-866_1787-852d others(17): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49034079 | |||||||
| chr3:49034079 | T | TTTATTAT others(11): Show |
1 | a0001c0001t0001g0002 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1787-869_1787-852d others(20): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49034079 | |||||||
| chr3:49034079 | T | TTTTTTA | 7 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(4): Show |
7 | HG02486.hp2 HG02559.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1787-852_1787-851i others(8): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49034079 | |||||||
| chr3:49034220 | A | G | 1 | a0001c0001t0001g0170 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1787-992T>C | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49034220 | |||||||
| chr3:49034391 | G | A | 1 | a0001c0001t0001g0217 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1787-1163C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49034391 | |||||||
| chr3:49034527 | C | A | 1 | a0001c0001t0001g0146 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1787-1299G>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49034527 | |||||||
| chr3:49034645 | C | T | 1 | a0001c0001t0001g0177 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1787-1417G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49034645 | |||||||
| chr3:49034660 | GT | G | 7 | a0001c0001t0001g0074 a0001c0001t0001g0081 a0001c0001t0001g0082 others(4): Show |
7 | HG01070.hp2 HG01192.hp1 HG01261.hp1 others(4): Show |
intron_variant | MODIFIER | c.1787-1433delA | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49034660 | |||||||
| chr3:49034752 | C | T | 1 | a0001c0001t0001g0162 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1787-1524G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49034752 | |||||||
| chr3:49034795 | T | C | 9 | a0002c0002t0001g0001 a0002c0002t0001g0039 a0002c0002t0001g0041 others(6): Show |
10 | HG00639.hp1 HG00733.hp2 HG00735.hp2 others(7): Show |
intron_variant | MODIFIER | c.1787-1567A>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49034795 | |||||||
| chr3:49034802 | A | C | 1 | a0001c0001t0002g0037 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1787-1574T>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49034802 | |||||||
| chr3:49035154 | C | G | 1 | a0001c0001t0001g0172 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1787-1926G>C | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49035154 | |||||||
| chr3:49035197 | A | G | 3 | a0001c0001t0001g0124 a0001c0001t0001g0161 a0001c0001t0001g0209 |
3 | HG01346.hp1 HG02615.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.1787-1969T>C | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49035197 | |||||||
| chr3:49035911 | C | CA | 28 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0013 others(25): Show |
28 | HG00544.hp2 HG00609.hp2 HG01516.hp2 others(25): Show |
intron_variant | MODIFIER | c.1787-2684dupT | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49035911 | |||||||
| chr3:49035911 | C | CAA | 14 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(11): Show |
15 | HG00639.hp1 HG00733.hp2 HG00735.hp2 others(12): Show |
intron_variant | MODIFIER | c.1787-2685_1787-268 others(6): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49035911 | |||||||
| chr3:49035922 | A | AC | 134 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(131): Show |
134 | HG00140.hp2 HG00280.hp2 HG00544.hp1 others(131): Show |
intron_variant | MODIFIER | c.1787-2695_1787-269 others(5): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49035922 | |||||||
| chr3:49035922 | A | C | 1 | a0001c0001t0001g0149 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1787-2694T>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49035922 | |||||||
| chr3:49035942 | G | C | 1 | a0002c0002t0001g0045 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1787-2714C>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49035942 | |||||||
| chr3:49036189 | A | G | 1 | a0001c0001t0001g0210 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1787-2961T>C | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49036189 | |||||||
| chr3:49036238 | T | C | 1 | a0001c0001t0001g0217 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1787-3010A>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49036238 | |||||||
| chr3:49036696 | C | CA | 5 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0202 others(2): Show |
5 | HG02486.hp2 HG02559.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.1787-3469dupT | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49036696 | |||||||
| chr3:49036696 | CA | C | 147 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(144): Show |
147 | HG00140.hp2 HG00280.hp2 HG00544.hp1 others(144): Show |
intron_variant | MODIFIER | c.1787-3469delT | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49036696 | |||||||
| chr3:49036714 | G | A | 5 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0001t0001g0107 others(2): Show |
5 | HG02615.hp1 HG02965.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.1787-3486C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49036714 | |||||||
| chr3:49037073 | T | TA | 128 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0033 others(125): Show |
128 | HG00140.hp2 HG00280.hp2 HG00544.hp1 others(125): Show |
intron_variant | MODIFIER | c.1787-3846dupT | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49037073 | |||||||
| chr3:49037073 | T | TAA | 6 | a0001c0001t0001g0142 a0001c0001t0001g0155 a0001c0001t0001g0156 others(3): Show |
6 | HG00735.hp1 HG01074.hp1 HG01981.hp1 others(3): Show |
intron_variant | MODIFIER | c.1787-3847_1787-384 others(6): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49037073 | |||||||
| chr3:49037073 | T | TAAA | 15 | a0002c0002t0001g0001 a0002c0002t0001g0011 a0002c0002t0001g0039 others(12): Show |
16 | HG00609.hp2 HG00639.hp1 HG00733.hp2 others(13): Show |
intron_variant | MODIFIER | c.1787-3848_1787-384 others(7): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49037073 | |||||||
| chr3:49037073 | TA | T | 5 | a0001c0001t0001g0036 a0001c0001t0001g0050 a0001c0001t0001g0053 others(2): Show |
5 | HG02735.hp2 HG02809.hp1 NA18951.hp2 others(2): Show |
intron_variant | MODIFIER | c.1787-3846delT | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49037073 | |||||||
| chr3:49037850 | G | A | 1 | a0001c0001t0001g0171 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1787-4622C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49037850 | |||||||
| chr3:49037939 | G | A | 1 | a0001c0001t0002g0037 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1787-4711C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49037939 | |||||||
| chr3:49038001 | A | T | 1 | a0001c0001t0001g0127 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1787-4773T>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49038001 | |||||||
| chr3:49038080 | A | T | 146 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(143): Show |
146 | HG00140.hp2 HG00280.hp2 HG00544.hp1 others(143): Show |
intron_variant | MODIFIER | c.1787-4852T>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49038080 | |||||||
| chr3:49038170 | C | T | 3 | a0001c0001t0002g0004 a0001c0001t0002g0218 a0001c0004t0002g0003 |
3 | HG03041.hp1 HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1787-4942G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49038170 | |||||||
| chr3:49038310 | T | G | 1 | a0001c0001t0001g0074 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1787-5082A>C | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49038310 | |||||||
| chr3:49038555 | C | G | 135 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(132): Show |
135 | HG00140.hp2 HG00280.hp2 HG00544.hp1 others(132): Show |
intron_variant | MODIFIER | c.1787-5327G>C | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49038555 | |||||||
| chr3:49038638 | T | C | 206 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(203): Show |
207 | HG00140.hp2 HG00280.hp2 HG00544.hp1 others(204): Show |
intron_variant | MODIFIER | c.1787-5410A>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49038638 | |||||||
| chr3:49038659 | G | A | 31 | a0001c0001t0001g0038 a0001c0001t0001g0049 a0001c0001t0001g0050 others(28): Show |
32 | HG00544.hp2 HG00609.hp2 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.1787-5431C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49038659 | |||||||
| chr3:49038764 | C | T | 2 | a0001c0001t0001g0006 a0001c0001t0001g0007 |
2 | HG01884.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1787-5536G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49038764 | |||||||
| chr3:49039249 | A | G | 3 | a0001c0001t0002g0004 a0001c0001t0002g0218 a0001c0004t0002g0003 |
3 | HG03041.hp1 HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1786+5141T>C | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49039249 | |||||||
| chr3:49039318 | T | C | 1 | a0001c0001t0002g0037 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1786+5072A>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49039318 | |||||||
| chr3:49039336 | G | A | 1 | a0001c0001t0005g0138 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1786+5054C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49039336 | |||||||
| chr3:49039446 | C | T | 1 | a0001c0001t0001g0092 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1786+4944G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49039446 | |||||||
| chr3:49039451 | C | A | 1 | a0001c0001t0001g0051 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1786+4939G>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49039451 | |||||||
| chr3:49039463 | T | C | 1 | a0001c0001t0001g0103 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1786+4927A>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49039463 | |||||||
| chr3:49039515 | C | T | 1 | a0001c0001t0001g0069 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1786+4875G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49039515 | |||||||
| chr3:49039517 | C | T | 3 | a0001c0001t0002g0004 a0001c0001t0002g0218 a0001c0004t0002g0003 |
3 | HG03041.hp1 HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1786+4873G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49039517 | |||||||
| chr3:49039618 | C | CA | 9 | a0001c0001t0001g0110 a0001c0001t0001g0152 a0001c0001t0001g0190 others(6): Show |
9 | HG00735.hp1 HG01243.hp2 HG02071.hp1 others(6): Show |
intron_variant | MODIFIER | c.1786+4771dupT | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49039618 | |||||||
| chr3:49039618 | CA | C | 6 | a0001c0001t0001g0019 a0001c0001t0001g0032 a0001c0001t0001g0078 others(3): Show |
6 | HG00733.hp1 HG01070.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1786+4771delT | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49039618 | |||||||
| chr3:49039727 | A | T | 1 | a0001c0001t0001g0115 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1786+4663T>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49039727 | |||||||
| chr3:49039762 | G | A | 4 | a0001c0001t0001g0013 a0001c0001t0001g0017 a0001c0001t0001g0026 others(1): Show |
4 | HG01261.hp2 HG01516.hp2 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.1786+4628C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49039762 | |||||||
| chr3:49039922 | C | T | 2 | a0001c0001t0001g0151 a0001c0001t0001g0152 |
2 | NA19003.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.1786+4468G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49039922 | |||||||
| chr3:49039987 | A | C | 5 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0125 others(2): Show |
5 | HG01192.hp2 HG01255.hp1 HG01928.hp1 others(2): Show |
intron_variant | MODIFIER | c.1786+4403T>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49039987 | |||||||
| chr3:49040001 | A | G | 1 | a0001c0001t0001g0211 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1786+4389T>C | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49040001 | |||||||
| chr3:49040333 | C | T | 1 | a0001c0001t0001g0156 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1786+4057G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49040333 | |||||||
| chr3:49040605 | T | C | 1 | a0001c0001t0001g0101 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1786+3785A>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49040605 | |||||||
| chr3:49040648 | C | T | 1 | a0001c0001t0001g0122 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1786+3742G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49040648 | |||||||
| chr3:49040961 | C | T | 3 | a0001c0001t0002g0004 a0001c0001t0002g0218 a0001c0004t0002g0003 |
3 | HG03041.hp1 HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1786+3429G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49040961 | |||||||
| chr3:49041050 | C | T | 1 | a0001c0001t0002g0218 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1786+3340G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49041050 | |||||||
| chr3:49041163 | T | G | 2 | a0001c0001t0001g0036 a0001c0001t0001g0147 |
2 | NA19012.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1786+3227A>C | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49041163 | |||||||
| chr3:49041339 | ATG | A | 138 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(135): Show |
138 | HG00140.hp2 HG00280.hp2 HG00544.hp1 others(135): Show |
intron_variant | MODIFIER | c.1786+3049_1786+305 others(6): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49041339 | |||||||
| chr3:49041491 | C | A | 5 | a0001c0001t0001g0002 a0001c0001t0001g0033 a0001c0001t0001g0034 others(2): Show |
5 | HG02145.hp1 HG02257.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.1786+2899G>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49041491 | |||||||
| chr3:49041618 | G | A | 1 | a0001c0001t0002g0037 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1786+2772C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49041618 | |||||||
| chr3:49041643 | T | C | 2 | a0001c0001t0001g0185 a0001c0001t0001g0186 |
2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1786+2747A>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49041643 | |||||||
| chr3:49041670 | ACTCAGGC others(460): Show |
A | 1 | a0001c0001t0001g0151 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1786+2253_1786+271 others(4): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49041670 | |||||||
| chr3:49041672 | T | C | 200 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(197): Show |
201 | HG00140.hp2 HG00280.hp2 HG00544.hp1 others(198): Show |
intron_variant | MODIFIER | c.1786+2718A>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49041672 | |||||||
| chr3:49041974 | T | C | 1 | a0002c0002t0001g0045 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1786+2416A>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49041974 | |||||||
| chr3:49042053 | G | A | 27 | a0001c0001t0001g0055 a0001c0001t0001g0070 a0001c0001t0001g0075 others(24): Show |
27 | HG00544.hp1 HG00735.hp1 HG01192.hp2 others(24): Show |
intron_variant | MODIFIER | c.1786+2337C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49042053 | |||||||
| chr3:49042062 | C | T | 1 | a0001c0001t0001g0210 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1786+2328G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49042062 | |||||||
| chr3:49042076 | G | GT | 22 | a0001c0001t0001g0012 a0001c0001t0001g0021 a0001c0001t0001g0033 others(19): Show |
22 | HG01099.hp1 HG01099.hp2 HG01192.hp2 others(19): Show |
intron_variant | MODIFIER | c.1786+2313dupA | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49042076 | |||||||
| chr3:49042095 | C | CG | 38 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0026 others(35): Show |
38 | HG01099.hp1 HG01099.hp2 HG01192.hp2 others(35): Show |
intron_variant | MODIFIER | c.1786+2294dupC | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49042095 | |||||||
| chr3:49042168 | G | A | 5 | a0001c0001t0001g0002 a0001c0001t0001g0033 a0001c0001t0001g0034 others(2): Show |
5 | HG02145.hp1 HG02257.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.1786+2222C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49042168 | |||||||
| chr3:49042444 | C | G | 5 | a0001c0001t0001g0002 a0001c0001t0001g0033 a0001c0001t0001g0034 others(2): Show |
5 | HG02145.hp1 HG02257.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.1786+1946G>C | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49042444 | |||||||
| chr3:49042466 | C | T | 1 | a0001c0001t0001g0145 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1786+1924G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49042466 | |||||||
| chr3:49042580 | G | T | 1 | a0001c0001t0002g0037 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1786+1810C>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49042580 | |||||||
| chr3:49042745 | G | T | 2 | a0001c0001t0001g0006 a0001c0001t0001g0007 |
2 | HG01884.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1786+1645C>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49042745 | |||||||
| chr3:49042785 | C | T | 2 | a0001c0001t0001g0085 a0001c0001t0001g0086 |
2 | HG01192.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.1786+1605G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49042785 | |||||||
| chr3:49043063 | A | G | 4 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0095 others(1): Show |
4 | HG00639.hp2 HG01256.hp2 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.1786+1327T>C | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49043063 | |||||||
| chr3:49043465 | C | T | 1 | a0001c0001t0001g0131 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1786+925G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49043465 | |||||||
| chr3:49043496 | C | CA | 86 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(83): Show |
86 | HG00140.hp2 HG00280.hp2 HG00639.hp2 others(83): Show |
intron_variant | MODIFIER | c.1786+893dupT | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49043496 | |||||||
| chr3:49043496 | C | CAA | 13 | a0001c0001t0001g0036 a0001c0001t0001g0080 a0001c0001t0001g0082 others(10): Show |
13 | HG01261.hp1 HG01981.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.1786+892_1786+893d others(4): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49043496 | |||||||
| chr3:49043496 | CA | C | 5 | a0001c0001t0001g0016 a0001c0001t0001g0028 a0001c0001t0001g0034 others(2): Show |
5 | HG01515.hp2 HG02145.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.1786+893delT | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49043496 | |||||||
| chr3:49043496 | CAAAAAAA others(3): Show |
C | 61 | a0001c0001t0001g0055 a0001c0001t0001g0070 a0001c0001t0001g0075 others(58): Show |
61 | HG00544.hp1 HG00609.hp1 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.1786+884_1786+893d others(12): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49043496 | |||||||
| chr3:49043496 | CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0001g0173 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1786+883_1786+893d others(13): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49043496 | |||||||
| chr3:49043554 | G | A | 1 | a0001c0001t0001g0083 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1786+836C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49043554 | |||||||
| chr3:49043814 | T | C | 146 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(143): Show |
146 | HG00140.hp2 HG00280.hp2 HG00544.hp1 others(143): Show |
intron_variant | MODIFIER | c.1786+576A>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49043814 | |||||||
| chr3:49044053 | G | C | 1 | a0001c0001t0001g0005 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1786+337C>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 6/9 | chr3 | 49044053 | |||||||
| chr3:49044609 | T | C | 1 | a0001c0001t0001g0088 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1672-105A>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 5/9 | chr3 | 49044609 | |||||||
| chr3:49044703 | G | A | 1 | a0001c0001t0001g0217 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1672-199C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 5/9 | chr3 | 49044703 | |||||||
| chr3:49044810 | A | G | 3 | a0001c0001t0002g0004 a0001c0001t0002g0218 a0001c0004t0002g0003 |
3 | HG03041.hp1 HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1672-306T>C | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 5/9 | chr3 | 49044810 | |||||||
| chr3:49044852 | C | CA | 7 | a0001c0001t0001g0073 a0001c0001t0001g0077 a0001c0001t0001g0078 others(4): Show |
7 | HG01243.hp1 HG02280.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1672-349dupT | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 5/9 | chr3 | 49044852 | |||||||
| chr3:49045011 | A | G | 7 | a0001c0001t0001g0073 a0001c0001t0001g0077 a0001c0001t0001g0078 others(4): Show |
7 | HG01243.hp1 HG02280.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1672-507T>C | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 5/9 | chr3 | 49045011 | |||||||
| chr3:49045326 | C | CA | 42 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0017 others(39): Show |
43 | HG00544.hp2 HG00609.hp2 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.1672-823dupT | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 5/9 | chr3 | 49045326 | |||||||
| chr3:49045326 | C | CAA | 22 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0056 others(19): Show |
22 | HG01074.hp2 HG01243.hp2 HG01517.hp2 others(19): Show |
intron_variant | MODIFIER | c.1672-824_1672-823d others(4): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 5/9 | chr3 | 49045326 | |||||||
| chr3:49045326 | CAAAA | C | 16 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(13): Show |
16 | HG01243.hp1 HG01952.hp1 HG02004.hp1 others(13): Show |
intron_variant | MODIFIER | c.1672-826_1672-823d others(6): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 5/9 | chr3 | 49045326 | |||||||
| chr3:49045326 | CAAAAA | C | 110 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(107): Show |
110 | HG00140.hp2 HG00280.hp2 HG00544.hp1 others(107): Show |
intron_variant | MODIFIER | c.1672-827_1672-823d others(7): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 5/9 | chr3 | 49045326 | |||||||
| chr3:49045512 | C | A | 1 | a0001c0001t0001g0035 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1671+913G>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 5/9 | chr3 | 49045512 | |||||||
| chr3:49045688 | C | T | 3 | a0001c0001t0002g0004 a0001c0001t0002g0218 a0001c0004t0002g0003 |
3 | HG03041.hp1 HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1671+737G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 5/9 | chr3 | 49045688 | |||||||
| chr3:49045831 | G | C | 2 | a0001c0001t0001g0130 a0001c0001t0001g0175 |
2 | HG02083.hp1 NA18961.hp2 |
intron_variant | MODIFIER | c.1671+594C>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 5/9 | chr3 | 49045831 | |||||||
| chr3:49045916 | C | T | 3 | a0001c0001t0002g0004 a0001c0001t0002g0218 a0001c0004t0002g0003 |
3 | HG03041.hp1 HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1671+509G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 5/9 | chr3 | 49045916 | |||||||
| chr3:49045991 | T | C | 2 | a0001c0001t0001g0111 a0001c0001t0001g0159 |
2 | HG02015.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.1671+434A>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 5/9 | chr3 | 49045991 | |||||||
| chr3:49046133 | G | A | 7 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0212 others(4): Show |
7 | HG00140.hp2 HG00280.hp2 HG01516.hp1 others(4): Show |
intron_variant | MODIFIER | c.1671+292C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 5/9 | chr3 | 49046133 | |||||||
| chr3:49046262 | T | TA | 46 | a0001c0001t0001g0055 a0001c0001t0001g0057 a0001c0001t0001g0070 others(43): Show |
47 | HG00544.hp1 HG00609.hp2 HG00639.hp1 others(44): Show |
intron_variant | MODIFIER | c.1671+162dupT | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 5/9 | chr3 | 49046262 | |||||||
| chr3:49046288 | T | C | 10 | a0001c0001t0001g0084 a0001c0001t0001g0118 a0001c0001t0001g0119 others(7): Show |
10 | HG00609.hp1 HG02015.hp2 HG02083.hp2 others(7): Show |
intron_variant | MODIFIER | c.1671+137A>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 5/9 | chr3 | 49046288 | |||||||
| chr3:49046833 | A | G | 1 | a0001c0001t0001g0196 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1516+236T>C | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 4/9 | chr3 | 49046833 | |||||||
| chr3:49046846 | G | A | 1 | a0001c0001t0001g0127 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1516+223C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 4/9 | chr3 | 49046846 | |||||||
| chr3:49047345 | G | GA | 6 | a0001c0001t0001g0055 a0001c0001t0001g0099 a0001c0001t0001g0121 others(3): Show |
6 | HG02071.hp2 NA18944.hp2 NA18951.hp1 others(3): Show |
intron_variant | MODIFIER | c.1339-100dupT | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49047345 | |||||||
| chr3:49047397 | T | C | 1 | a0001c0001t0001g0097 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1339-151A>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49047397 | |||||||
| chr3:49047424 | C | T | 1 | a0001c0001t0002g0004 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1339-178G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49047424 | |||||||
| chr3:49047479 | G | GT | 27 | a0001c0001t0001g0002 a0001c0001t0001g0033 a0001c0001t0001g0035 others(24): Show |
27 | HG00140.hp2 HG01928.hp2 HG01952.hp1 others(24): Show |
intron_variant | MODIFIER | c.1339-234dupA | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49047479 | |||||||
| chr3:49047479 | GT | G | 6 | a0001c0001t0001g0050 a0001c0001t0001g0056 a0001c0001t0001g0057 others(3): Show |
6 | HG02735.hp2 HG03453.hp2 HG06807.hp2 others(3): Show |
intron_variant | MODIFIER | c.1339-234delA | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49047479 | |||||||
| chr3:49047541 | T | C | 1 | a0001c0001t0001g0025 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1339-295A>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49047541 | |||||||
| chr3:49047640 | C | T | 1 | a0001c0001t0001g0007 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1339-394G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49047640 | |||||||
| chr3:49047679 | C | T | 1 | a0001c0001t0001g0198 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1339-433G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49047679 | |||||||
| chr3:49047779 | G | A | 1 | a0001c0001t0001g0104 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1339-533C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49047779 | |||||||
| chr3:49047893 | C | G | 4 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(1): Show |
4 | HG01243.hp1 HG02622.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1339-647G>C | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49047893 | |||||||
| chr3:49048040 | C | T | 1 | a0001c0001t0001g0142 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1339-794G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49048040 | |||||||
| chr3:49048063 | TG | T | 3 | a0001c0001t0002g0004 a0001c0001t0002g0218 a0001c0004t0002g0003 |
3 | HG03041.hp1 HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1339-818delC | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49048063 | |||||||
| chr3:49048118 | ATTTC | A | 3 | a0001c0001t0002g0004 a0001c0001t0002g0218 a0001c0004t0002g0003 |
3 | HG03041.hp1 HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1339-876_1339-873d others(6): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49048118 | |||||||
| chr3:49048130 | CT | C | 136 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(133): Show |
136 | HG00140.hp2 HG00280.hp2 HG00544.hp1 others(133): Show |
intron_variant | MODIFIER | c.1339-885delA | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49048130 | |||||||
| chr3:49048196 | G | T | 1 | a0001c0001t0002g0037 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1339-950C>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49048196 | |||||||
| chr3:49048289 | C | T | 1 | a0001c0001t0001g0136 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1339-1043G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49048289 | |||||||
| chr3:49048382 | C | A | 2 | a0001c0001t0001g0013 a0001c0001t0001g0030 |
2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1339-1136G>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49048382 | |||||||
| chr3:49048477 | T | TA | 8 | a0001c0001t0001g0015 a0001c0001t0001g0036 a0001c0001t0001g0190 others(5): Show |
8 | HG01243.hp2 HG02559.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1339-1232dupT | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49048477 | |||||||
| chr3:49048490 | A | C | 137 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(134): Show |
137 | HG00140.hp2 HG00280.hp2 HG00544.hp1 others(134): Show |
intron_variant | MODIFIER | c.1339-1244T>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49048490 | |||||||
| chr3:49048498 | A | C | 29 | a0001c0001t0001g0038 a0001c0001t0001g0049 a0001c0001t0001g0050 others(26): Show |
30 | HG00544.hp2 HG00609.hp2 HG00639.hp1 others(27): Show |
intron_variant | MODIFIER | c.1339-1252T>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49048498 | |||||||
| chr3:49048780 | T | TC | 201 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(198): Show |
202 | HG00140.hp2 HG00280.hp2 HG00544.hp1 others(199): Show |
intron_variant | MODIFIER | c.1339-1535dupG | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49048780 | |||||||
| chr3:49048782 | T | C | 201 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(198): Show |
202 | HG00140.hp2 HG00280.hp2 HG00544.hp1 others(199): Show |
intron_variant | MODIFIER | c.1339-1536A>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49048782 | |||||||
| chr3:49048801 | C | CA | 7 | a0001c0001t0001g0088 a0001c0001t0001g0111 a0001c0001t0001g0159 others(4): Show |
7 | HG02015.hp1 HG02818.hp2 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.1339-1556dupT | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49048801 | |||||||
| chr3:49048826 | C | T | 21 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0189 others(18): Show |
21 | HG01074.hp2 HG01243.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.1339-1580G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49048826 | |||||||
| chr3:49048954 | T | C | 4 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0156 others(1): Show |
4 | HG02109.hp1 HG02970.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.1339-1708A>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49048954 | |||||||
| chr3:49049004 | C | G | 1 | a0001c0003t0001g0094 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1339-1758G>C | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49049004 | |||||||
| chr3:49049140 | C | A | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG02015.hp2 HG02083.hp2 |
intron_variant | MODIFIER | c.1339-1894G>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49049140 | |||||||
| chr3:49049297 | T | C | 1 | a0001c0001t0001g0060 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1339-2051A>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49049297 | |||||||
| chr3:49049377 | G | A | 1 | a0001c0001t0001g0136 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1339-2131C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49049377 | |||||||
| chr3:49049694 | C | A | 1 | a0002c0002t0001g0040 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1339-2448G>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49049694 | |||||||
| chr3:49049696 | C | A | 1 | a0002c0002t0001g0040 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1339-2450G>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49049696 | |||||||
| chr3:49049697 | C | A | 1 | a0002c0002t0001g0040 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1339-2451G>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49049697 | |||||||
| chr3:49049698 | A | T | 1 | a0002c0002t0001g0040 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1339-2452T>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49049698 | |||||||
| chr3:49049700 | G | T | 1 | a0002c0002t0001g0040 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1339-2454C>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49049700 | |||||||
| chr3:49049703 | G | A | 1 | a0002c0002t0001g0040 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1339-2457C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49049703 | |||||||
| chr3:49049704 | G | A | 1 | a0002c0002t0001g0040 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1339-2458C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49049704 | |||||||
| chr3:49049705 | C | T | 1 | a0002c0002t0001g0040 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1339-2459G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49049705 | |||||||
| chr3:49049706 | C | T | 1 | a0002c0002t0001g0040 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1339-2460G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49049706 | |||||||
| chr3:49049708 | G | A | 1 | a0002c0002t0001g0040 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1339-2462C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49049708 | |||||||
| chr3:49049709 | G | A | 1 | a0002c0002t0001g0040 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1339-2463C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49049709 | |||||||
| chr3:49049713 | G | A | 1 | a0002c0002t0001g0040 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1339-2467C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49049713 | |||||||
| chr3:49049715 | C | A | 1 | a0002c0002t0001g0040 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1339-2469G>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49049715 | |||||||
| chr3:49049716 | T | A | 1 | a0002c0002t0001g0040 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1339-2470A>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49049716 | |||||||
| chr3:49049718 | A | T | 1 | a0002c0002t0001g0040 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1339-2472T>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49049718 | |||||||
| chr3:49049725 | C | A | 1 | a0002c0002t0001g0040 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1339-2479G>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49049725 | |||||||
| chr3:49049726 | G | A | 1 | a0002c0002t0001g0040 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1339-2480C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49049726 | |||||||
| chr3:49049727 | A | G | 1 | a0002c0002t0001g0040 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1339-2481T>C | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49049727 | |||||||
| chr3:49049729 | C | A | 1 | a0002c0002t0001g0040 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1339-2483G>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49049729 | |||||||
| chr3:49049730 | T | A | 1 | a0002c0002t0001g0040 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1339-2484A>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49049730 | |||||||
| chr3:49049733 | G | A | 1 | a0002c0002t0001g0040 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1339-2487C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49049733 | |||||||
| chr3:49049734 | G | A | 1 | a0002c0002t0001g0040 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1339-2488C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49049734 | |||||||
| chr3:49049735 | T | A | 1 | a0002c0002t0001g0040 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1339-2489A>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49049735 | |||||||
| chr3:49049738 | T | A | 1 | a0002c0002t0001g0040 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1339-2492A>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49049738 | |||||||
| chr3:49049739 | C | G | 1 | a0002c0002t0001g0040 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1339-2493G>C | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49049739 | |||||||
| chr3:49049741 | G | A | 3 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0001c0001t0001g0168 |
3 | HG01099.hp2 HG01168.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.1339-2495C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49049741 | |||||||
| chr3:49049741 | G | C | 1 | a0002c0002t0001g0040 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1339-2495C>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49049741 | |||||||
| chr3:49049742 | T | A | 1 | a0002c0002t0001g0040 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1339-2496A>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49049742 | |||||||
| chr3:49049744 | T | A | 1 | a0002c0002t0001g0040 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1339-2498A>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49049744 | |||||||
| chr3:49049745 | G | A | 1 | a0002c0002t0001g0040 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1339-2499C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49049745 | |||||||
| chr3:49049746 | C | G | 1 | a0002c0002t0001g0040 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1339-2500G>C | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49049746 | |||||||
| chr3:49049747 | C | A | 1 | a0002c0002t0001g0040 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1339-2501G>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49049747 | |||||||
| chr3:49049748 | T | C | 1 | a0002c0002t0001g0040 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1339-2502A>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49049748 | |||||||
| chr3:49049750 | G | A | 1 | a0002c0002t0001g0040 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1339-2504C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49049750 | |||||||
| chr3:49049751 | G | A | 1 | a0002c0002t0001g0040 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1339-2505C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49049751 | |||||||
| chr3:49049752 | C | T | 1 | a0002c0002t0001g0040 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1339-2506G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49049752 | |||||||
| chr3:49049753 | C | A | 1 | a0002c0002t0001g0040 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1339-2507G>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49049753 | |||||||
| chr3:49049756 | C | T | 1 | a0002c0002t0001g0040 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1339-2510G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49049756 | |||||||
| chr3:49049757 | C | T | 1 | a0002c0002t0001g0040 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1339-2511G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49049757 | |||||||
| chr3:49049771 | T | G | 1 | a0002c0002t0001g0040 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1339-2525A>C | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49049771 | |||||||
| chr3:49049772 | A | G | 1 | a0002c0002t0001g0040 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1339-2526T>C | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49049772 | |||||||
| chr3:49049778 | G | A | 31 | a0001c0001t0001g0038 a0001c0001t0001g0049 a0001c0001t0001g0050 others(28): Show |
32 | HG00544.hp2 HG00609.hp2 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.1339-2532C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49049778 | |||||||
| chr3:49049779 | T | A | 1 | a0002c0002t0001g0040 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1339-2533A>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49049779 | |||||||
| chr3:49049793 | C | T | 1 | a0001c0001t0001g0096 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1339-2547G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49049793 | |||||||
| chr3:49050248 | C | CA | 10 | a0001c0001t0001g0026 a0001c0001t0001g0036 a0001c0001t0001g0051 others(7): Show |
10 | HG00544.hp2 HG01261.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1339-3003dupT | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49050248 | |||||||
| chr3:49050248 | C | CAA | 11 | a0001c0001t0001g0018 a0001c0001t0001g0021 a0001c0001t0001g0022 others(8): Show |
11 | HG00140.hp1 HG00280.hp1 HG01255.hp2 others(8): Show |
intron_variant | MODIFIER | c.1339-3004_1339-300 others(6): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49050248 | |||||||
| chr3:49050248 | C | CAAAAAAA others(3): Show |
1 | a0001c0001t0001g0081 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1339-3012_1339-300 others(14): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49050248 | |||||||
| chr3:49050248 | C | CAAAAAAA others(4): Show |
3 | a0001c0001t0001g0149 a0001c0001t0001g0213 a0001c0001t0001g0217 |
3 | HG01516.hp1 HG03453.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1339-3013_1339-300 others(15): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49050248 | |||||||
| chr3:49050248 | C | CAAAAAAA others(5): Show |
1 | a0001c0001t0001g0153 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1339-3014_1339-300 others(16): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49050248 | |||||||
| chr3:49050248 | C | CAAAAAAA others(6): Show |
3 | a0001c0001t0001g0071 a0001c0001t0001g0088 a0001c0001t0001g0150 |
3 | HG02809.hp1 HG02818.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1339-3015_1339-300 others(17): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49050248 | |||||||
| chr3:49050248 | C | CAAAAAAA others(7): Show |
1 | a0001c0001t0001g0072 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1339-3016_1339-300 others(18): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49050248 | |||||||
| chr3:49050248 | C | CAAAAAAA others(8): Show |
5 | a0001c0001t0001g0105 a0001c0001t0001g0154 a0001c0001t0001g0155 others(2): Show |
5 | HG02109.hp1 HG02965.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1339-3017_1339-300 others(19): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49050248 | |||||||
| chr3:49050248 | C | CAAAAAAA others(9): Show |
1 | a0001c0001t0003g0221 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1339-3018_1339-300 others(20): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49050248 | |||||||
| chr3:49050248 | C | CAAAAAAA others(11): Show |
1 | a0001c0001t0001g0080 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1339-3020_1339-300 others(22): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49050248 | |||||||
| chr3:49050248 | C | CAAAAAAA others(14): Show |
2 | a0001c0001t0001g0073 a0001c0001t0001g0216 |
2 | HG02145.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1339-3023_1339-300 others(25): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49050248 | |||||||
| chr3:49050248 | C | CAAAAAAA others(15): Show |
1 | a0001c0001t0001g0212 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1339-3024_1339-300 others(26): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49050248 | |||||||
| chr3:49050248 | C | CAAAAAAA others(17): Show |
2 | a0001c0001t0001g0074 a0001c0001t0001g0141 |
2 | HG02451.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.1339-3026_1339-300 others(28): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49050248 | |||||||
| chr3:49050248 | C | CAAAAAAA others(18): Show |
2 | a0001c0001t0001g0082 a0001c0001t0001g0090 |
2 | HG01261.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.1339-3027_1339-300 others(29): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49050248 | |||||||
| chr3:49050248 | C | CAAAAAAA others(20): Show |
1 | a0001c0001t0001g0210 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1339-3003_1339-300 others(31): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49050248 | |||||||
| chr3:49050248 | C | CAAAAAAA others(22): Show |
1 | a0001c0001t0001g0087 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1339-3003_1339-300 others(33): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49050248 | |||||||
| chr3:49050248 | C | CAAAAAAA others(25): Show |
1 | a0001c0001t0001g0131 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1339-3003_1339-300 others(36): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49050248 | |||||||
| chr3:49050248 | C | CAAAAAAA others(26): Show |
1 | a0001c0001t0001g0079 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1339-3003_1339-300 others(37): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49050248 | |||||||
| chr3:49050248 | C | CAAAAAAA others(29): Show |
2 | a0001c0001t0001g0106 a0001c0001t0001g0107 |
2 | HG02976.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1339-3003_1339-300 others(40): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49050248 | |||||||
| chr3:49050248 | C | CAAAAAAA others(30): Show |
1 | a0001c0001t0001g0091 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1339-3003_1339-300 others(41): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49050248 | |||||||
| chr3:49050248 | CAAA | C | 5 | a0001c0001t0001g0108 a0001c0001t0001g0172 a0001c0001t0001g0174 others(2): Show |
5 | HG00738.hp1 HG00738.hp2 HG03942.hp1 others(2): Show |
intron_variant | MODIFIER | c.1339-3005_1339-300 others(7): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49050248 | |||||||
| chr3:49050248 | CAAAA | C | 93 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0055 others(90): Show |
93 | HG00544.hp1 HG00609.hp1 HG00735.hp1 others(90): Show |
intron_variant | MODIFIER | c.1339-3006_1339-300 others(8): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49050248 | |||||||
| chr3:49050248 | CAAAAA | C | 7 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0033 others(4): Show |
7 | HG00639.hp2 HG02145.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1339-3007_1339-300 others(9): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49050248 | |||||||
| chr3:49050422 | C | CA | 33 | a0001c0001t0001g0012 a0001c0001t0001g0036 a0001c0001t0001g0038 others(30): Show |
34 | HG00544.hp2 HG00609.hp2 HG00639.hp1 others(31): Show |
intron_variant | MODIFIER | c.1339-3177dupT | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49050422 | |||||||
| chr3:49050422 | C | CAA | 8 | a0001c0001t0001g0201 a0001c0001t0002g0004 a0001c0001t0002g0218 others(5): Show |
8 | HG01070.hp1 HG03041.hp1 HG03453.hp2 others(5): Show |
intron_variant | MODIFIER | c.1339-3178_1339-317 others(6): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49050422 | |||||||
| chr3:49050422 | CA | C | 113 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(110): Show |
113 | HG00140.hp2 HG00280.hp2 HG00544.hp1 others(110): Show |
intron_variant | MODIFIER | c.1339-3177delT | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49050422 | |||||||
| chr3:49050422 | CAA | C | 6 | a0001c0001t0001g0068 a0001c0001t0001g0105 a0001c0001t0001g0125 others(3): Show |
6 | HG00738.hp1 HG00738.hp2 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1339-3178_1339-317 others(6): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49050422 | |||||||
| chr3:49050422 | CAAAAAAA others(6): Show |
C | 3 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0001c0001t0001g0168 |
3 | HG01099.hp2 HG01168.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.1339-3189_1339-317 others(17): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49050422 | |||||||
| chr3:49050503 | C | T | 1 | a0001c0004t0002g0003 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1339-3257G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49050503 | |||||||
| chr3:49050527 | C | A | 2 | a0001c0001t0001g0071 a0001c0001t0001g0072 |
2 | HG02809.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1339-3281G>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49050527 | |||||||
| chr3:49050579 | G | A | 3 | a0001c0001t0002g0004 a0001c0001t0002g0218 a0001c0004t0002g0003 |
3 | HG03041.hp1 HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1339-3333C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49050579 | |||||||
| chr3:49050592 | A | G | 1 | a0001c0001t0001g0084 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1339-3346T>C | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49050592 | |||||||
| chr3:49050679 | T | C | 135 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(132): Show |
135 | HG00140.hp2 HG00280.hp2 HG00544.hp1 others(132): Show |
intron_variant | MODIFIER | c.1339-3433A>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49050679 | |||||||
| chr3:49050694 | AAAC | A | 198 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(195): Show |
199 | HG00140.hp2 HG00280.hp2 HG00544.hp1 others(196): Show |
intron_variant | MODIFIER | c.1339-3451_1339-344 others(7): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49050694 | |||||||
| chr3:49050923 | T | A | 31 | a0001c0001t0001g0038 a0001c0001t0001g0049 a0001c0001t0001g0050 others(28): Show |
32 | HG00544.hp2 HG00609.hp2 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.1339-3677A>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49050923 | |||||||
| chr3:49050926 | A | G | 1 | a0001c0001t0001g0124 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1339-3680T>C | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49050926 | |||||||
| chr3:49050986 | T | C | 3 | a0001c0001t0002g0004 a0001c0001t0002g0218 a0001c0004t0002g0003 |
3 | HG03041.hp1 HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1339-3740A>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49050986 | |||||||
| chr3:49051161 | C | T | 1 | a0001c0001t0006g0120 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1339-3915G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49051161 | |||||||
| chr3:49051238 | C | T | 1 | a0001c0001t0001g0078 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1339-3992G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49051238 | |||||||
| chr3:49051324 | T | C | 1 | a0001c0001t0001g0209 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1339-4078A>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49051324 | |||||||
| chr3:49051344 | G | T | 1 | a0001c0001t0001g0170 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1339-4098C>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49051344 | |||||||
| chr3:49051584 | G | GC | 43 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0012 others(40): Show |
43 | HG00140.hp1 HG00280.hp1 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.1339-4339dupG | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49051584 | |||||||
| chr3:49051584 | G | GCC | 40 | a0001c0001t0001g0015 a0001c0001t0001g0038 a0001c0001t0001g0049 others(37): Show |
41 | HG00544.hp2 HG00733.hp2 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.1339-4340_1339-433 others(6): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49051584 | |||||||
| chr3:49051584 | GC | G | 36 | a0001c0001t0001g0006 a0001c0001t0001g0033 a0001c0001t0001g0034 others(33): Show |
36 | HG00280.hp2 HG01070.hp2 HG01074.hp1 others(33): Show |
intron_variant | MODIFIER | c.1339-4339delG | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49051584 | |||||||
| chr3:49051587 | C | G | 1 | a0001c0001t0001g0208 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1339-4341G>C | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49051587 | |||||||
| chr3:49051594 | C | A | 1 | a0001c0001t0001g0170 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1339-4348G>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49051594 | |||||||
| chr3:49051631 | C | G | 5 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0001g0087 others(2): Show |
5 | HG01070.hp2 HG01192.hp1 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.1339-4385G>C | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49051631 | |||||||
| chr3:49051634 | A | C | 2 | a0001c0001t0001g0214 a0001c0001t0001g0215 |
2 | HG02602.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.1339-4388T>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49051634 | |||||||
| chr3:49051694 | G | A | 1 | a0001c0001t0001g0070 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1339-4448C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49051694 | |||||||
| chr3:49051935 | G | A | 1 | a0001c0001t0001g0177 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1339-4689C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49051935 | |||||||
| chr3:49052004 | A | G | 1 | a0001c0001t0001g0029 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1339-4758T>C | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49052004 | |||||||
| chr3:49052023 | G | A | 1 | a0001c0001t0001g0194 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1339-4777C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49052023 | |||||||
| chr3:49052294 | C | A | 1 | a0001c0001t0001g0014 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1338+4568G>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49052294 | |||||||
| chr3:49052340 | G | A | 1 | a0001c0001t0001g0110 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1338+4522C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49052340 | |||||||
| chr3:49052911 | T | C | 2 | a0001c0001t0001g0139 a0001c0003t0001g0094 |
2 | NA18944.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.1338+3951A>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49052911 | |||||||
| chr3:49053070 | C | A | 1 | a0001c0001t0001g0114 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1338+3792G>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49053070 | |||||||
| chr3:49053187 | G | T | 1 | a0001c0001t0001g0114 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1338+3675C>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49053187 | |||||||
| chr3:49053263 | T | C | 147 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(144): Show |
147 | HG00140.hp2 HG00280.hp2 HG00544.hp1 others(144): Show |
intron_variant | MODIFIER | c.1338+3599A>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49053263 | |||||||
| chr3:49053486 | C | CA | 145 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(142): Show |
145 | HG00140.hp2 HG00280.hp2 HG00544.hp1 others(142): Show |
intron_variant | MODIFIER | c.1338+3375dupT | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49053486 | |||||||
| chr3:49053486 | C | CAA | 54 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(51): Show |
55 | HG00639.hp1 HG00639.hp2 HG00733.hp2 others(52): Show |
intron_variant | MODIFIER | c.1338+3374_1338+337 others(6): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49053486 | |||||||
| chr3:49053486 | C | CAAA | 5 | a0001c0001t0001g0036 a0001c0001t0001g0139 a0001c0001t0001g0167 others(2): Show |
5 | HG01515.hp1 HG01517.hp2 NA18944.hp1 others(2): Show |
intron_variant | MODIFIER | c.1338+3373_1338+337 others(7): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49053486 | |||||||
| chr3:49053506 | C | A | 1 | a0002c0002t0003g0220 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1338+3356G>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49053506 | |||||||
| chr3:49053507 | A | G | 3 | a0001c0001t0002g0004 a0001c0001t0002g0218 a0001c0004t0002g0003 |
3 | HG03041.hp1 HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1338+3355T>C | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49053507 | |||||||
| chr3:49053990 | G | A | 1 | a0001c0001t0001g0090 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1338+2872C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49053990 | |||||||
| chr3:49054270 | T | C | 4 | a0001c0001t0001g0093 a0001c0001t0001g0116 a0001c0001t0001g0133 others(1): Show |
4 | HG02622.hp2 HG02630.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1338+2592A>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49054270 | |||||||
| chr3:49054339 | G | A | 22 | a0001c0001t0001g0036 a0001c0001t0001g0187 a0001c0001t0001g0188 others(19): Show |
22 | HG01074.hp2 HG01243.hp2 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.1338+2523C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49054339 | |||||||
| chr3:49054659 | T | C | 1 | a0001c0001t0002g0037 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1338+2203A>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49054659 | |||||||
| chr3:49055005 | A | G | 1 | a0001c0001t0002g0218 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1338+1857T>C | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49055005 | |||||||
| chr3:49055241 | T | G | 1 | a0001c0001t0002g0218 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1338+1621A>C | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49055241 | |||||||
| chr3:49055515 | T | C | 3 | a0001c0001t0002g0004 a0001c0001t0002g0218 a0001c0004t0002g0003 |
3 | HG03041.hp1 HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1338+1347A>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49055515 | |||||||
| chr3:49055586 | C | T | 1 | a0001c0001t0001g0141 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1338+1276G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49055586 | |||||||
| chr3:49055648 | C | A | 4 | a0001c0001t0001g0038 a0001c0001t0001g0049 a0001c0001t0001g0050 others(1): Show |
4 | HG00544.hp2 HG02735.hp2 NA18963.hp2 others(1): Show |
intron_variant | MODIFIER | c.1338+1214G>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49055648 | |||||||
| chr3:49055944 | A | G | 201 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(198): Show |
202 | HG00140.hp2 HG00280.hp2 HG00544.hp1 others(199): Show |
intron_variant | MODIFIER | c.1338+918T>C | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49055944 | |||||||
| chr3:49056124 | T | C | 1 | a0001c0001t0001g0127 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1338+738A>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49056124 | |||||||
| chr3:49056177 | T | C | 2 | a0001c0001t0001g0008 a0001c0001t0001g0180 |
2 | NA18747.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.1338+685A>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49056177 | |||||||
| chr3:49056234 | A | G | 1 | a0001c0001t0001g0126 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1338+628T>C | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49056234 | |||||||
| chr3:49056272 | C | A | 1 | a0001c0001t0001g0049 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1338+590G>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49056272 | |||||||
| chr3:49056279 | C | T | 1 | a0001c0001t0001g0141 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1338+583G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49056279 | |||||||
| chr3:49056504 | T | G | 1 | a0001c0001t0001g0166 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1338+358A>C | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49056504 | |||||||
| chr3:49056505 | A | C | 1 | a0001c0001t0001g0166 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1338+357T>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49056505 | |||||||
| chr3:49056505 | A | G | 1 | a0001c0001t0001g0217 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1338+357T>C | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 3/9 | chr3 | 49056505 | |||||||
| chr3:49058158 | T | A | 1 | a0002c0002t0001g0011 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.310-268A>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49058158 | |||||||
| chr3:49058256 | T | C | 1 | a0001c0001t0001g0060 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.310-366A>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49058256 | |||||||
| chr3:49058613 | G | A | 3 | a0001c0001t0002g0004 a0001c0001t0002g0218 a0001c0004t0002g0003 |
3 | HG03041.hp1 HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.310-723C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49058613 | |||||||
| chr3:49058662 | CTT | C | 5 | a0001c0001t0001g0002 a0001c0001t0001g0033 a0001c0001t0001g0034 others(2): Show |
5 | HG02145.hp1 HG02257.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.310-774_310-773del others(2): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49058662 | |||||||
| chr3:49058961 | CT | C | 34 | a0001c0001t0001g0030 a0001c0001t0001g0038 a0001c0001t0001g0049 others(31): Show |
35 | HG00544.hp2 HG00609.hp2 HG00639.hp1 others(32): Show |
intron_variant | MODIFIER | c.310-1072delA | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49058961 | |||||||
| chr3:49059002 | C | T | 1 | a0001c0001t0001g0199 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.310-1112G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49059002 | |||||||
| chr3:49059055 | G | A | 5 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0149 others(2): Show |
5 | HG02809.hp1 HG02886.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.310-1165C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49059055 | |||||||
| chr3:49059105 | G | A | 1 | a0001c0001t0001g0209 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.310-1215C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49059105 | |||||||
| chr3:49059415 | C | A | 135 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(132): Show |
135 | HG00140.hp2 HG00280.hp2 HG00544.hp1 others(132): Show |
intron_variant | MODIFIER | c.310-1525G>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49059415 | |||||||
| chr3:49059606 | G | A | 1 | a0001c0001t0001g0108 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.310-1716C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49059606 | |||||||
| chr3:49059626 | G | A | 3 | a0001c0001t0002g0004 a0001c0001t0002g0218 a0001c0004t0002g0003 |
3 | HG03041.hp1 HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.310-1736C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49059626 | |||||||
| chr3:49059715 | C | T | 1 | a0001c0001t0001g0110 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.310-1825G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49059715 | |||||||
| chr3:49059794 | C | T | 2 | a0001c0001t0001g0164 a0001c0001t0005g0138 |
2 | HG04115.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.310-1904G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49059794 | |||||||
| chr3:49059901 | T | C | 2 | a0001c0001t0001g0074 a0001c0001t0001g0141 |
2 | HG02451.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.310-2011A>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49059901 | |||||||
| chr3:49059988 | G | A | 1 | a0001c0001t0001g0005 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.310-2098C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49059988 | |||||||
| chr3:49060041 | C | T | 1 | a0001c0001t0001g0108 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.310-2151G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49060041 | |||||||
| chr3:49060149 | C | T | 137 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(134): Show |
137 | HG00140.hp2 HG00280.hp2 HG00544.hp1 others(134): Show |
intron_variant | MODIFIER | c.310-2259G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49060149 | |||||||
| chr3:49060267 | C | A | 3 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0001g0087 |
3 | HG01070.hp2 HG01192.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.310-2377G>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49060267 | |||||||
| chr3:49060322 | T | C | 5 | a0001c0001t0001g0002 a0001c0001t0001g0033 a0001c0001t0001g0034 others(2): Show |
5 | HG02145.hp1 HG02257.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.310-2432A>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49060322 | |||||||
| chr3:49060328 | G | T | 1 | a0001c0001t0001g0115 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.310-2438C>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49060328 | |||||||
| chr3:49060350 | C | T | 135 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(132): Show |
135 | HG00140.hp2 HG00280.hp2 HG00544.hp1 others(132): Show |
intron_variant | MODIFIER | c.310-2460G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49060350 | |||||||
| chr3:49060519 | G | A | 3 | a0001c0001t0001g0124 a0001c0001t0001g0161 a0001c0001t0001g0209 |
3 | HG01346.hp1 HG02615.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.310-2629C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49060519 | |||||||
| chr3:49060695 | C | T | 1 | a0001c0001t0001g0016 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.310-2805G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49060695 | |||||||
| chr3:49060980 | T | C | 1 | a0001c0001t0001g0007 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.310-3090A>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49060980 | |||||||
| chr3:49061134 | T | TA | 15 | a0001c0001t0001g0025 a0001c0001t0001g0030 a0001c0001t0001g0032 others(12): Show |
16 | HG00280.hp1 HG00609.hp2 HG00733.hp1 others(13): Show |
intron_variant | MODIFIER | c.310-3245dupT | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49061134 | |||||||
| chr3:49061134 | T | TAAA | 6 | a0002c0002t0001g0043 a0002c0002t0001g0044 a0002c0002t0003g0220 others(3): Show |
6 | HG02071.hp1 NA18747.hp2 NA18954.hp1 others(3): Show |
intron_variant | MODIFIER | c.310-3247_310-3245d others(5): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49061134 | |||||||
| chr3:49061134 | TA | T | 23 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0019 others(20): Show |
23 | HG00609.hp1 HG01516.hp2 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.310-3245delT | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49061134 | |||||||
| chr3:49061134 | TAA | T | 10 | a0001c0001t0001g0038 a0001c0001t0001g0051 a0001c0001t0001g0052 others(7): Show |
10 | HG02071.hp2 HG02280.hp2 HG03098.hp2 others(7): Show |
intron_variant | MODIFIER | c.310-3246_310-3245d others(4): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49061134 | |||||||
| chr3:49061134 | TAAA | T | 26 | a0001c0001t0001g0006 a0001c0001t0001g0055 a0001c0001t0001g0070 others(23): Show |
26 | HG00140.hp2 HG01074.hp1 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.310-3247_310-3245d others(5): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49061134 | |||||||
| chr3:49061134 | TAAAA | T | 96 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(93): Show |
96 | HG00280.hp2 HG00544.hp1 HG00639.hp2 others(93): Show |
intron_variant | MODIFIER | c.310-3248_310-3245d others(6): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49061134 | |||||||
| chr3:49061134 | TAAAAA | T | 7 | a0001c0001t0001g0002 a0001c0001t0001g0034 a0001c0001t0001g0060 others(4): Show |
7 | HG01192.hp2 HG01255.hp1 HG01928.hp1 others(4): Show |
intron_variant | MODIFIER | c.310-3249_310-3245d others(7): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49061134 | |||||||
| chr3:49061134 | TAAAAAAA others(7): Show |
T | 1 | a0001c0001t0001g0146 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.310-3258_310-3245d others(16): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49061134 | |||||||
| chr3:49061308 | C | T | 1 | a0001c0001t0002g0218 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.310-3418G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49061308 | |||||||
| chr3:49061743 | T | C | 1 | a0001c0001t0001g0051 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.310-3853A>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49061743 | |||||||
| chr3:49062002 | G | A | 3 | a0001c0001t0002g0004 a0001c0001t0002g0218 a0001c0004t0002g0003 |
3 | HG03041.hp1 HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.310-4112C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49062002 | |||||||
| chr3:49062163 | T | C | 14 | a0001c0001t0001g0070 a0001c0001t0001g0085 a0001c0001t0001g0086 others(11): Show |
14 | HG01192.hp2 HG01255.hp1 HG01928.hp1 others(11): Show |
intron_variant | MODIFIER | c.310-4273A>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49062163 | |||||||
| chr3:49062282 | G | A | 1 | a0001c0001t0001g0217 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.310-4392C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49062282 | |||||||
| chr3:49062372 | C | CT | 12 | a0001c0001t0001g0002 a0001c0001t0001g0053 a0001c0001t0001g0061 others(9): Show |
12 | HG00735.hp1 HG01346.hp2 HG02004.hp1 others(9): Show |
intron_variant | MODIFIER | c.310-4483dupA | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49062372 | |||||||
| chr3:49062516 | A | G | 2 | a0002c0002t0001g0044 a0002c0002t0001g0064 |
2 | NA18747.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.310-4626T>C | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49062516 | |||||||
| chr3:49062729 | C | T | 1 | a0001c0001t0001g0166 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.310-4839G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49062729 | |||||||
| chr3:49062730 | G | A | 1 | a0001c0001t0001g0217 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.310-4840C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49062730 | |||||||
| chr3:49062776 | G | A | 2 | a0001c0001t0001g0185 a0001c0001t0001g0186 |
2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.310-4886C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49062776 | |||||||
| chr3:49062831 | C | G | 1 | a0001c0001t0001g0002 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.310-4941G>C | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49062831 | |||||||
| chr3:49062831 | C | T | 2 | a0001c0001t0002g0004 a0001c0004t0002g0003 |
2 | HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.310-4941G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49062831 | |||||||
| chr3:49062842 | T | C | 1 | a0002c0002t0001g0045 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.310-4952A>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49062842 | |||||||
| chr3:49062872 | T | C | 201 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(198): Show |
202 | HG00140.hp2 HG00280.hp2 HG00544.hp1 others(199): Show |
intron_variant | MODIFIER | c.310-4982A>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49062872 | |||||||
| chr3:49062957 | G | A | 1 | a0001c0004t0002g0003 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.310-5067C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49062957 | |||||||
| chr3:49063128 | G | C | 1 | a0001c0001t0002g0004 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.310-5238C>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49063128 | |||||||
| chr3:49064183 | G | A | 1 | a0001c0001t0003g0219 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.310-6293C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49064183 | |||||||
| chr3:49064234 | A | AT | 21 | a0001c0001t0001g0017 a0001c0001t0001g0036 a0001c0001t0001g0061 others(18): Show |
21 | HG00735.hp2 HG01261.hp1 HG02083.hp1 others(18): Show |
intron_variant | MODIFIER | c.310-6345dupA | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49064234 | |||||||
| chr3:49064234 | AT | A | 11 | a0001c0001t0001g0009 a0001c0001t0001g0095 a0001c0001t0001g0107 others(8): Show |
11 | HG01256.hp1 HG01256.hp2 HG01496.hp1 others(8): Show |
intron_variant | MODIFIER | c.310-6345delA | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49064234 | |||||||
| chr3:49064234 | ATTTTTTT others(4): Show |
A | 4 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(1): Show |
4 | HG01243.hp1 HG02622.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.310-6355_310-6345d others(13): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49064234 | |||||||
| chr3:49064356 | C | T | 1 | a0001c0001t0009g0222 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.310-6466G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49064356 | |||||||
| chr3:49064568 | A | T | 201 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(198): Show |
202 | HG00140.hp2 HG00280.hp2 HG00544.hp1 others(199): Show |
intron_variant | MODIFIER | c.310-6678T>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49064568 | |||||||
| chr3:49064681 | C | T | 1 | a0001c0001t0001g0027 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.310-6791G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49064681 | |||||||
| chr3:49064801 | A | G | 3 | a0001c0001t0002g0004 a0001c0001t0002g0218 a0001c0004t0002g0003 |
3 | HG03041.hp1 HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.310-6911T>C | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49064801 | |||||||
| chr3:49064843 | C | T | 3 | a0001c0001t0002g0004 a0001c0001t0002g0218 a0001c0004t0002g0003 |
3 | HG03041.hp1 HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.310-6953G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49064843 | |||||||
| chr3:49065103 | A | G | 1 | a0001c0001t0006g0120 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.310-7213T>C | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49065103 | |||||||
| chr3:49065346 | T | C | 1 | a0001c0001t0001g0198 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.310-7456A>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49065346 | |||||||
| chr3:49065538 | TCA | T | 2 | a0001c0001t0001g0075 a0001c0001t0001g0076 |
2 | NA18963.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.310-7650_310-7649d others(4): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49065538 | |||||||
| chr3:49065568 | A | G | 1 | a0001c0001t0001g0055 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.310-7678T>C | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49065568 | |||||||
| chr3:49065809 | T | C | 1 | a0001c0001t0001g0051 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.310-7919A>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49065809 | |||||||
| chr3:49066244 | T | C | 1 | a0001c0001t0001g0196 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.310-8354A>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49066244 | |||||||
| chr3:49066281 | C | T | 3 | a0001c0001t0002g0004 a0001c0001t0002g0218 a0001c0004t0002g0003 |
3 | HG03041.hp1 HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.310-8391G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49066281 | |||||||
| chr3:49066434 | T | G | 1 | a0001c0001t0001g0179 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.310-8544A>C | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49066434 | |||||||
| chr3:49066443 | T | C | 1 | a0001c0001t0001g0083 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.310-8553A>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49066443 | |||||||
| chr3:49066460 | CT | C | 3 | a0001c0001t0002g0004 a0001c0001t0002g0218 a0001c0004t0002g0003 |
3 | HG03041.hp1 HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.310-8571delA | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49066460 | |||||||
| chr3:49066466 | T | C | 3 | a0001c0001t0002g0004 a0001c0001t0002g0218 a0001c0004t0002g0003 |
3 | HG03041.hp1 HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.310-8576A>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49066466 | |||||||
| chr3:49066476 | T | G | 2 | a0001c0001t0001g0091 a0001c0001t0001g0174 |
2 | HG00738.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.310-8586A>C | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49066476 | |||||||
| chr3:49066558 | G | A | 1 | a0001c0001t0001g0146 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.310-8668C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49066558 | |||||||
| chr3:49066583 | GCCT | G | 6 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(3): Show |
6 | HG02809.hp1 HG02886.hp1 HG06807.hp1 others(3): Show |
intron_variant | MODIFIER | c.310-8696_310-8694d others(5): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49066583 | |||||||
| chr3:49066701 | C | T | 2 | a0001c0001t0001g0068 a0001c0001t0001g0172 |
2 | HG00738.hp1 HG01257.hp1 |
intron_variant | MODIFIER | c.310-8811G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49066701 | |||||||
| chr3:49066843 | G | C | 5 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0001t0001g0107 others(2): Show |
5 | HG02615.hp1 HG02965.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.310-8953C>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49066843 | |||||||
| chr3:49066864 | C | A | 1 | a0001c0001t0001g0016 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.310-8974G>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49066864 | |||||||
| chr3:49066964 | G | C | 1 | a0001c0001t0001g0036 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.310-9074C>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49066964 | |||||||
| chr3:49066969 | C | T | 3 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0069 |
3 | NA19003.hp1 NA19012.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.310-9079G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49066969 | |||||||
| chr3:49067149 | C | T | 1 | a0001c0001t0001g0005 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.310-9259G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49067149 | |||||||
| chr3:49067395 | G | A | 1 | a0001c0001t0001g0007 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.309+9314C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49067395 | |||||||
| chr3:49067703 | A | G | 146 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(143): Show |
146 | HG00140.hp2 HG00280.hp2 HG00544.hp1 others(143): Show |
intron_variant | MODIFIER | c.309+9006T>C | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49067703 | |||||||
| chr3:49067964 | T | A | 23 | a0001c0001t0001g0005 a0001c0001t0001g0036 a0001c0001t0001g0187 others(20): Show |
23 | HG01074.hp2 HG01243.hp2 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.309+8745A>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49067964 | |||||||
| chr3:49068108 | T | C | 1 | a0001c0001t0001g0036 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.309+8601A>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49068108 | |||||||
| chr3:49068294 | C | T | 2 | a0001c0001t0001g0151 a0001c0001t0001g0152 |
2 | NA19003.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.309+8415G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49068294 | |||||||
| chr3:49068357 | T | A | 1 | a0002c0002t0001g0011 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.309+8352A>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49068357 | |||||||
| chr3:49068432 | T | C | 1 | a0001c0001t0001g0062 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.309+8277A>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49068432 | |||||||
| chr3:49068450 | T | A | 1 | a0001c0001t0001g0060 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.309+8259A>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49068450 | |||||||
| chr3:49068453 | G | A | 1 | a0001c0001t0001g0016 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.309+8256C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49068453 | |||||||
| chr3:49068454 | T | A | 4 | a0001c0001t0001g0217 a0001c0001t0002g0004 a0001c0001t0002g0218 others(1): Show |
4 | HG03041.hp1 HG03453.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.309+8255A>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49068454 | |||||||
| chr3:49068466 | T | TA | 180 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(177): Show |
181 | HG00140.hp2 HG00280.hp2 HG00544.hp1 others(178): Show |
intron_variant | MODIFIER | c.309+8242dupT | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49068466 | |||||||
| chr3:49068466 | T | TAA | 6 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0033 others(3): Show |
6 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.309+8241_309+8242d others(4): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49068466 | |||||||
| chr3:49068634 | C | T | 2 | a0001c0001t0001g0217 a0001c0001t0002g0218 |
2 | HG03041.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.309+8075G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49068634 | |||||||
| chr3:49068753 | T | C | 28 | a0001c0001t0001g0055 a0001c0001t0001g0070 a0001c0001t0001g0075 others(25): Show |
28 | HG00544.hp1 HG00735.hp1 HG01192.hp2 others(25): Show |
intron_variant | MODIFIER | c.309+7956A>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49068753 | |||||||
| chr3:49068908 | G | A | 6 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(3): Show |
6 | HG02809.hp1 HG02886.hp1 HG06807.hp1 others(3): Show |
intron_variant | MODIFIER | c.309+7801C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49068908 | |||||||
| chr3:49068942 | A | C | 1 | a0001c0001t0001g0114 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.309+7767T>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49068942 | |||||||
| chr3:49069098 | A | T | 2 | a0002c0002t0004g0223 a0002c0002t0004g0225 |
2 | NA19057.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.309+7611T>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49069098 | |||||||
| chr3:49069101 | A | AT | 10 | a0001c0001t0001g0002 a0001c0001t0001g0035 a0001c0001t0001g0066 others(7): Show |
10 | HG01099.hp2 HG02965.hp2 HG02970.hp2 others(7): Show |
intron_variant | MODIFIER | c.309+7607dupA | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49069101 | |||||||
| chr3:49069101 | A | T | 19 | a0001c0001t0001g0051 a0002c0002t0001g0001 a0002c0002t0001g0039 others(16): Show |
20 | HG00609.hp2 HG00639.hp1 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.309+7608T>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49069101 | |||||||
| chr3:49069103 | TA | T | 6 | a0001c0001t0001g0056 a0001c0001t0001g0110 a0001c0001t0001g0136 others(3): Show |
6 | HG03017.hp1 HG03471.hp2 HG03492.hp2 others(3): Show |
intron_variant | MODIFIER | c.309+7605delT | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49069103 | |||||||
| chr3:49069104 | A | AT | 22 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(19): Show |
22 | HG00609.hp1 HG00639.hp2 HG00738.hp1 others(19): Show |
intron_variant | MODIFIER | c.309+7604dupA | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49069104 | |||||||
| chr3:49069104 | A | T | 33 | a0001c0001t0001g0002 a0001c0001t0001g0035 a0001c0001t0001g0038 others(30): Show |
34 | HG00544.hp2 HG00609.hp2 HG00639.hp1 others(31): Show |
intron_variant | MODIFIER | c.309+7605T>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49069104 | |||||||
| chr3:49069107 | A | AT | 33 | a0001c0001t0001g0006 a0001c0001t0001g0033 a0001c0001t0001g0034 others(30): Show |
33 | HG00140.hp2 HG01192.hp1 HG01192.hp2 others(30): Show |
intron_variant | MODIFIER | c.309+7601dupA | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49069107 | |||||||
| chr3:49069107 | A | T | 68 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(65): Show |
69 | HG00544.hp2 HG00609.hp1 HG00609.hp2 others(66): Show |
intron_variant | MODIFIER | c.309+7602T>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49069107 | |||||||
| chr3:49069107 | AT | A | 21 | a0001c0001t0001g0036 a0001c0001t0001g0187 a0001c0001t0001g0188 others(18): Show |
21 | HG01074.hp2 HG01243.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.309+7601delA | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49069107 | |||||||
| chr3:49069109 | T | TA | 65 | a0001c0001t0001g0007 a0001c0001t0001g0055 a0001c0001t0001g0070 others(62): Show |
65 | HG00280.hp2 HG00544.hp1 HG00735.hp1 others(62): Show |
intron_variant | MODIFIER | c.309+7599_309+7600i others(3): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49069109 | |||||||
| chr3:49069110 | T | A | 4 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0109 others(1): Show |
4 | HG01168.hp2 HG02723.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.309+7599A>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49069110 | |||||||
| chr3:49069111 | T | A | 1 | a0001c0001t0001g0207 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.309+7598A>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49069111 | |||||||
| chr3:49069112 | T | A | 7 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0001g0108 others(4): Show |
7 | HG02083.hp1 HG03942.hp1 NA18522.hp1 others(4): Show |
intron_variant | MODIFIER | c.309+7597A>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49069112 | |||||||
| chr3:49069113 | T | A | 1 | a0001c0001t0002g0037 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.309+7596A>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49069113 | |||||||
| chr3:49069124 | G | T | 1 | a0001c0001t0001g0100 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.309+7585C>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49069124 | |||||||
| chr3:49069292 | C | T | 4 | a0001c0001t0001g0217 a0001c0001t0002g0004 a0001c0001t0002g0218 others(1): Show |
4 | HG03041.hp1 HG03453.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.309+7417G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49069292 | |||||||
| chr3:49069296 | G | T | 2 | a0001c0001t0001g0013 a0001c0001t0001g0030 |
2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.309+7413C>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49069296 | |||||||
| chr3:49069543 | A | AT | 156 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(153): Show |
156 | HG00140.hp2 HG00280.hp2 HG00544.hp1 others(153): Show |
intron_variant | MODIFIER | c.309+7165dupA | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49069543 | |||||||
| chr3:49069543 | A | ATT | 12 | a0001c0001t0001g0069 a0001c0001t0001g0090 a0001c0001t0001g0091 others(9): Show |
12 | HG01496.hp1 HG01981.hp2 HG02129.hp2 others(9): Show |
intron_variant | MODIFIER | c.309+7164_309+7165d others(4): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49069543 | |||||||
| chr3:49070038 | A | AT | 7 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0131 others(4): Show |
7 | HG00735.hp1 HG01261.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.309+6670dupA | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49070038 | |||||||
| chr3:49070101 | G | A | 2 | a0001c0001t0001g0139 a0001c0003t0001g0094 |
2 | NA18944.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.309+6608C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49070101 | |||||||
| chr3:49070133 | G | A | 1 | a0001c0001t0001g0008 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.309+6576C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49070133 | |||||||
| chr3:49070145 | C | G | 1 | a0001c0001t0001g0171 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.309+6564G>C | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49070145 | |||||||
| chr3:49070226 | T | C | 1 | a0001c0001t0001g0183 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.309+6483A>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49070226 | |||||||
| chr3:49070280 | C | T | 1 | a0001c0001t0001g0166 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.309+6429G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49070280 | |||||||
| chr3:49070335 | G | A | 2 | a0001c0001t0001g0068 a0001c0001t0001g0172 |
2 | HG00738.hp1 HG01257.hp1 |
intron_variant | MODIFIER | c.309+6374C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49070335 | |||||||
| chr3:49070418 | C | T | 2 | a0001c0001t0001g0006 a0001c0001t0001g0007 |
2 | HG01884.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.309+6291G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49070418 | |||||||
| chr3:49070861 | A | G | 4 | a0001c0001t0001g0217 a0001c0001t0002g0004 a0001c0001t0002g0218 others(1): Show |
4 | HG03041.hp1 HG03453.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.309+5848T>C | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49070861 | |||||||
| chr3:49070995 | T | C | 178 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(175): Show |
179 | HG00140.hp2 HG00280.hp2 HG00544.hp1 others(176): Show |
intron_variant | MODIFIER | c.309+5714A>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49070995 | |||||||
| chr3:49071068 | CT | C | 138 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(135): Show |
138 | HG00140.hp2 HG00280.hp2 HG00544.hp1 others(135): Show |
intron_variant | MODIFIER | c.309+5640delA | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49071068 | |||||||
| chr3:49071104 | G | T | 1 | a0001c0001t0001g0162 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.309+5605C>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49071104 | |||||||
| chr3:49071166 | G | A | 2 | a0001c0001t0001g0006 a0001c0001t0001g0007 |
2 | HG01884.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.309+5543C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49071166 | |||||||
| chr3:49071228 | C | T | 1 | a0001c0001t0001g0091 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.309+5481G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49071228 | |||||||
| chr3:49071452 | A | G | 1 | a0001c0001t0001g0110 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.309+5257T>C | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49071452 | |||||||
| chr3:49071634 | G | A | 1 | a0001c0001t0001g0015 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.309+5075C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49071634 | |||||||
| chr3:49071846 | C | T | 1 | a0001c0001t0001g0162 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.309+4863G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49071846 | |||||||
| chr3:49072086 | T | C | 1 | a0001c0001t0001g0217 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.309+4623A>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49072086 | |||||||
| chr3:49072152 | G | A | 31 | a0001c0001t0001g0038 a0001c0001t0001g0049 a0001c0001t0001g0050 others(28): Show |
32 | HG00544.hp2 HG00609.hp2 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.309+4557C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49072152 | |||||||
| chr3:49072160 | A | T | 137 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(134): Show |
137 | HG00140.hp2 HG00280.hp2 HG00544.hp1 others(134): Show |
intron_variant | MODIFIER | c.309+4549T>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49072160 | |||||||
| chr3:49072191 | C | T | 3 | a0001c0001t0002g0004 a0001c0001t0002g0218 a0001c0004t0002g0003 |
3 | HG03041.hp1 HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.309+4518G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49072191 | |||||||
| chr3:49072192 | G | A | 4 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0095 others(1): Show |
4 | HG00639.hp2 HG01256.hp2 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.309+4517C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49072192 | |||||||
| chr3:49072486 | G | A | 178 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(175): Show |
179 | HG00140.hp2 HG00280.hp2 HG00544.hp1 others(176): Show |
intron_variant | MODIFIER | c.309+4223C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49072486 | |||||||
| chr3:49073278 | C | T | 1 | a0002c0002t0001g0043 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.309+3431G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49073278 | |||||||
| chr3:49073456 | T | C | 206 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(203): Show |
207 | HG00140.hp2 HG00280.hp2 HG00544.hp1 others(204): Show |
intron_variant | MODIFIER | c.309+3253A>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49073456 | |||||||
| chr3:49073625 | T | A | 1 | a0001c0001t0001g0057 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.309+3084A>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49073625 | |||||||
| chr3:49073626 | A | T | 1 | a0001c0001t0001g0057 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.309+3083T>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49073626 | |||||||
| chr3:49073760 | T | C | 1 | a0001c0001t0001g0176 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.309+2949A>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49073760 | |||||||
| chr3:49073834 | A | G | 3 | a0001c0001t0001g0124 a0001c0001t0001g0161 a0001c0001t0001g0209 |
3 | HG01346.hp1 HG02615.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.309+2875T>C | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49073834 | |||||||
| chr3:49074077 | T | C | 5 | a0001c0001t0001g0002 a0001c0001t0001g0033 a0001c0001t0001g0034 others(2): Show |
5 | HG02145.hp1 HG02257.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.309+2632A>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49074077 | |||||||
| chr3:49074126 | C | A | 1 | a0001c0001t0001g0055 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.309+2583G>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49074126 | |||||||
| chr3:49074320 | C | T | 1 | a0001c0001t0001g0080 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.309+2389G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49074320 | |||||||
| chr3:49074429 | A | G | 3 | a0001c0001t0001g0109 a0001c0001t0001g0126 a0001c0001t0001g0158 |
3 | HG01168.hp2 HG01256.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.309+2280T>C | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49074429 | |||||||
| chr3:49074639 | C | A | 1 | a0001c0001t0001g0010 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.309+2070G>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49074639 | |||||||
| chr3:49074745 | G | A | 5 | a0001c0001t0001g0002 a0001c0001t0001g0033 a0001c0001t0001g0034 others(2): Show |
5 | HG02145.hp1 HG02257.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.309+1964C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49074745 | |||||||
| chr3:49074913 | A | G | 1 | a0001c0001t0001g0141 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.309+1796T>C | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49074913 | |||||||
| chr3:49074999 | C | T | 4 | a0001c0001t0001g0217 a0001c0001t0002g0004 a0001c0001t0002g0218 others(1): Show |
4 | HG03041.hp1 HG03453.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.309+1710G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49074999 | |||||||
| chr3:49075025 | C | T | 2 | a0001c0001t0001g0135 a0001c0001t0001g0144 |
2 | HG00609.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.309+1684G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49075025 | |||||||
| chr3:49075154 | T | C | 1 | a0001c0001t0001g0102 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.309+1555A>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49075154 | |||||||
| chr3:49075295 | C | T | 1 | a0001c0001t0001g0137 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.309+1414G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49075295 | |||||||
| chr3:49075330 | C | CA | 9 | a0001c0001t0001g0065 a0001c0001t0001g0098 a0001c0001t0001g0123 others(6): Show |
9 | HG00544.hp2 HG02071.hp2 HG02074.hp1 others(6): Show |
intron_variant | MODIFIER | c.309+1378dupT | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49075330 | |||||||
| chr3:49075330 | CA | C | 7 | a0001c0001t0001g0105 a0001c0001t0001g0126 a0001c0001t0001g0176 others(4): Show |
7 | HG01256.hp1 HG02965.hp2 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.309+1378delT | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49075330 | |||||||
| chr3:49075401 | A | G | 1 | a0001c0001t0001g0217 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.309+1308T>C | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49075401 | |||||||
| chr3:49075488 | G | A | 1 | a0001c0001t0003g0219 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.309+1221C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49075488 | |||||||
| chr3:49075568 | T | C | 2 | a0001c0001t0001g0164 a0001c0001t0005g0138 |
2 | HG04115.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.309+1141A>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49075568 | |||||||
| chr3:49075651 | A | AAAC | 31 | a0001c0001t0001g0038 a0001c0001t0001g0049 a0001c0001t0001g0050 others(28): Show |
32 | HG00544.hp2 HG00609.hp2 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.309+1057_309+1058i others(5): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49075651 | |||||||
| chr3:49075966 | G | A | 1 | a0001c0001t0001g0176 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.309+743C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49075966 | |||||||
| chr3:49076235 | T | C | 31 | a0001c0001t0001g0038 a0001c0001t0001g0049 a0001c0001t0001g0050 others(28): Show |
32 | HG00544.hp2 HG00609.hp2 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.309+474A>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49076235 | |||||||
| chr3:49076280 | C | A | 31 | a0001c0001t0001g0038 a0001c0001t0001g0049 a0001c0001t0001g0050 others(28): Show |
32 | HG00544.hp2 HG00609.hp2 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.309+429G>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49076280 | |||||||
| chr3:49076296 | C | T | 9 | a0002c0002t0001g0001 a0002c0002t0001g0039 a0002c0002t0001g0041 others(6): Show |
10 | HG00639.hp1 HG00733.hp2 HG00735.hp2 others(7): Show |
intron_variant | MODIFIER | c.309+413G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49076296 | |||||||
| chr3:49076322 | G | C | 1 | a0001c0001t0002g0037 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.309+387C>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49076322 | |||||||
| chr3:49076404 | G | A | 1 | a0001c0001t0001g0167 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.309+305C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49076404 | |||||||
| chr3:49076488 | T | C | 1 | a0001c0001t0002g0037 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.309+221A>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49076488 | |||||||
| chr3:49076524 | TA | T | 200 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(197): Show |
201 | HG00140.hp2 HG00280.hp2 HG00544.hp1 others(198): Show |
intron_variant | MODIFIER | c.309+184delT | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49076524 | |||||||
| chr3:49076632 | TGATG | T | 31 | a0001c0001t0001g0038 a0001c0001t0001g0049 a0001c0001t0001g0050 others(28): Show |
32 | HG00544.hp2 HG00609.hp2 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.309+73_309+76delCA others(2): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 2/9 | chr3 | 49076632 | |||||||
| chr3:49077111 | C | T | 137 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(134): Show |
137 | HG00140.hp2 HG00280.hp2 HG00544.hp1 others(134): Show |
intron_variant | MODIFIER | c.-21-73G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49077111 | |||||||
| chr3:49077680 | T | C | 1 | a0001c0001t0001g0209 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-21-642A>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49077680 | |||||||
| chr3:49077957 | C | G | 1 | a0001c0001t0001g0162 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-21-919G>C | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49077957 | |||||||
| chr3:49078095 | A | C | 1 | a0001c0001t0001g0217 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-21-1057T>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49078095 | |||||||
| chr3:49078386 | C | CT | 113 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0009 others(110): Show |
113 | HG00140.hp2 HG00280.hp2 HG00544.hp1 others(110): Show |
intron_variant | MODIFIER | c.-21-1349dupA | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49078386 | |||||||
| chr3:49078386 | C | CTT | 26 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0069 others(23): Show |
26 | HG00609.hp1 HG00735.hp1 HG01496.hp2 others(23): Show |
intron_variant | MODIFIER | c.-21-1350_-21-1349d others(4): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49078386 | |||||||
| chr3:49078386 | CT | C | 11 | a0001c0001t0001g0112 a0001c0001t0002g0037 a0002c0002t0001g0001 others(8): Show |
12 | HG00639.hp1 HG00733.hp2 HG00735.hp2 others(9): Show |
intron_variant | MODIFIER | c.-21-1349delA | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49078386 | |||||||
| chr3:49078515 | C | T | 31 | a0001c0001t0001g0038 a0001c0001t0001g0049 a0001c0001t0001g0050 others(28): Show |
32 | HG00544.hp2 HG00609.hp2 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.-21-1477G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49078515 | |||||||
| chr3:49078694 | C | CT | 25 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0033 others(22): Show |
25 | HG00544.hp1 HG00735.hp1 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.-21-1657dupA | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49078694 | |||||||
| chr3:49078694 | CT | C | 23 | a0001c0001t0001g0173 a0001c0001t0001g0187 a0001c0001t0001g0189 others(20): Show |
23 | HG01074.hp2 HG01243.hp2 HG02486.hp2 others(20): Show |
intron_variant | MODIFIER | c.-21-1657delA | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49078694 | |||||||
| chr3:49079001 | C | T | 1 | a0001c0001t0001g0127 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-21-1963G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49079001 | |||||||
| chr3:49079134 | C | A | 1 | a0001c0001t0001g0108 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-21-2096G>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49079134 | |||||||
| chr3:49079237 | A | C | 2 | a0001c0001t0001g0091 a0001c0001t0001g0184 |
2 | HG02280.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-21-2199T>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49079237 | |||||||
| chr3:49079458 | T | C | 2 | a0002c0002t0001g0040 a0002c0002t0001g0063 |
2 | HG00609.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.-21-2420A>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49079458 | |||||||
| chr3:49079748 | G | A | 1 | a0001c0001t0001g0197 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-21-2710C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49079748 | |||||||
| chr3:49080028 | C | CA | 160 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(157): Show |
161 | HG00140.hp2 HG00280.hp2 HG00544.hp1 others(158): Show |
intron_variant | MODIFIER | c.-21-2991dupT | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49080028 | |||||||
| chr3:49080028 | C | CAA | 5 | a0001c0001t0001g0084 a0001c0001t0001g0102 a0001c0001t0001g0151 others(2): Show |
5 | HG01981.hp1 HG03704.hp1 HG03942.hp2 others(2): Show |
intron_variant | MODIFIER | c.-21-2992_-21-2991d others(4): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49080028 | |||||||
| chr3:49080139 | G | T | 1 | a0001c0001t0001g0006 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-21-3101C>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49080139 | |||||||
| chr3:49080216 | G | A | 1 | a0001c0001t0001g0005 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-21-3178C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49080216 | |||||||
| chr3:49080217 | A | T | 2 | a0001c0001t0001g0185 a0001c0001t0001g0186 |
2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-21-3179T>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49080217 | |||||||
| chr3:49080580 | G | T | 6 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(3): Show |
6 | HG02809.hp1 HG02886.hp1 HG06807.hp1 others(3): Show |
intron_variant | MODIFIER | c.-21-3542C>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49080580 | |||||||
| chr3:49080622 | C | T | 1 | a0002c0002t0001g0041 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-21-3584G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49080622 | |||||||
| chr3:49080854 | T | C | 1 | a0001c0001t0001g0153 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-21-3816A>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49080854 | |||||||
| chr3:49080966 | C | CA | 97 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(94): Show |
97 | HG00544.hp1 HG00609.hp1 HG00609.hp2 others(94): Show |
intron_variant | MODIFIER | c.-21-3929dupT | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49080966 | |||||||
| chr3:49080966 | C | CAA | 55 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0049 others(52): Show |
56 | HG00544.hp2 HG00639.hp1 HG00733.hp2 others(53): Show |
intron_variant | MODIFIER | c.-21-3930_-21-3929d others(4): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49080966 | |||||||
| chr3:49081203 | G | A | 21 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0189 others(18): Show |
21 | HG01074.hp2 HG01243.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.-21-4165C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49081203 | |||||||
| chr3:49081279 | T | C | 2 | a0001c0001t0001g0006 a0001c0001t0001g0007 |
2 | HG01884.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.-21-4241A>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49081279 | |||||||
| chr3:49081413 | T | A | 2 | a0001c0001t0001g0167 a0001c0001t0001g0171 |
2 | NA18961.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.-21-4375A>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49081413 | |||||||
| chr3:49081414 | C | T | 2 | a0001c0001t0001g0167 a0001c0001t0001g0171 |
2 | NA18961.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.-21-4376G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49081414 | |||||||
| chr3:49081416 | TA | T | 13 | a0001c0001t0001g0008 a0001c0001t0001g0072 a0001c0001t0001g0081 others(10): Show |
13 | HG01070.hp2 HG01496.hp2 HG01515.hp1 others(10): Show |
intron_variant | MODIFIER | c.-21-4379delT | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49081416 | |||||||
| chr3:49081421 | A | G | 1 | a0001c0001t0002g0037 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-21-4383T>C | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49081421 | |||||||
| chr3:49081811 | A | AT | 9 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0069 others(6): Show |
9 | HG01515.hp1 HG02572.hp2 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.-21-4774dupA | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49081811 | |||||||
| chr3:49082007 | C | T | 1 | a0001c0001t0001g0166 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.-21-4969G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49082007 | |||||||
| chr3:49082179 | C | T | 1 | a0001c0001t0001g0104 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-21-5141G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49082179 | |||||||
| chr3:49082219 | G | A | 2 | a0001c0001t0001g0139 a0001c0003t0001g0094 |
2 | NA18944.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.-21-5181C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49082219 | |||||||
| chr3:49082573 | T | C | 6 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0095 others(3): Show |
6 | HG00639.hp2 HG01256.hp2 HG01346.hp2 others(3): Show |
intron_variant | MODIFIER | c.-21-5535A>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49082573 | |||||||
| chr3:49082607 | A | G | 27 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(24): Show |
27 | HG00639.hp2 HG00738.hp1 HG01099.hp2 others(24): Show |
intron_variant | MODIFIER | c.-21-5569T>C | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49082607 | |||||||
| chr3:49082694 | G | GACC | 10 | a0001c0001t0001g0038 a0001c0001t0001g0049 a0001c0001t0001g0050 others(7): Show |
10 | HG00544.hp2 HG02280.hp2 HG02735.hp2 others(7): Show |
intron_variant | MODIFIER | c.-21-5659_-21-5657d others(5): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49082694 | |||||||
| chr3:49082811 | C | T | 2 | a0001c0001t0002g0004 a0001c0004t0002g0003 |
2 | HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-21-5773G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49082811 | |||||||
| chr3:49082838 | T | C | 1 | a0001c0001t0001g0137 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-21-5800A>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49082838 | |||||||
| chr3:49082894 | CA | C | 9 | a0001c0001t0001g0015 a0001c0001t0001g0033 a0001c0001t0001g0034 others(6): Show |
9 | HG01515.hp1 HG02145.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.-21-5857delT | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49082894 | |||||||
| chr3:49083183 | C | T | 1 | a0002c0002t0001g0040 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.-21-6145G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49083183 | |||||||
| chr3:49083204 | C | CA | 106 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0009 others(103): Show |
106 | HG00140.hp2 HG00280.hp2 HG00544.hp1 others(103): Show |
intron_variant | MODIFIER | c.-21-6167dupT | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49083204 | |||||||
| chr3:49083204 | C | CAA | 7 | a0001c0001t0001g0080 a0001c0001t0001g0083 a0001c0001t0001g0092 others(4): Show |
7 | HG02129.hp2 HG02622.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.-21-6168_-21-6167d others(4): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49083204 | |||||||
| chr3:49083220 | A | AAG | 18 | a0001c0001t0001g0055 a0001c0001t0001g0074 a0001c0001t0001g0077 others(15): Show |
18 | HG01192.hp1 HG01192.hp2 HG01496.hp1 others(15): Show |
intron_variant | MODIFIER | c.-21-6183_-21-6182i others(4): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49083220 | |||||||
| chr3:49083220 | A | G | 1 | a0002c0002t0001g0064 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.-21-6182T>C | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49083220 | |||||||
| chr3:49083221 | G | A | 8 | a0001c0001t0001g0035 a0001c0001t0001g0072 a0001c0001t0001g0073 others(5): Show |
8 | HG02004.hp1 HG02886.hp1 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.-21-6183C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49083221 | |||||||
| chr3:49083222 | G | C | 1 | a0001c0001t0001g0215 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-21-6184C>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49083222 | |||||||
| chr3:49083301 | T | A | 1 | a0001c0001t0001g0198 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-21-6263A>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49083301 | |||||||
| chr3:49083370 | G | T | 1 | a0001c0001t0001g0006 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-21-6332C>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49083370 | |||||||
| chr3:49083469 | T | C | 1 | a0001c0001t0002g0004 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-21-6431A>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49083469 | |||||||
| chr3:49083664 | G | A | 1 | a0001c0001t0001g0175 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.-21-6626C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49083664 | |||||||
| chr3:49083992 | G | A | 1 | a0001c0001t0001g0217 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-21-6954C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49083992 | |||||||
| chr3:49084380 | A | G | 4 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0156 others(1): Show |
4 | HG02109.hp1 HG02970.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.-21-7342T>C | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49084380 | |||||||
| chr3:49084661 | G | A | 10 | a0001c0001t0001g0084 a0001c0001t0001g0118 a0001c0001t0001g0119 others(7): Show |
10 | HG00609.hp1 HG02015.hp2 HG02083.hp2 others(7): Show |
intron_variant | MODIFIER | c.-21-7623C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49084661 | |||||||
| chr3:49084688 | C | T | 6 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(3): Show |
6 | HG01243.hp1 HG02280.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-21-7650G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49084688 | |||||||
| chr3:49084695 | C | T | 1 | a0001c0001t0001g0036 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-21-7657G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49084695 | |||||||
| chr3:49084823 | A | T | 3 | a0001c0001t0002g0004 a0001c0001t0002g0218 a0001c0004t0002g0003 |
3 | HG03041.hp1 HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-21-7785T>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49084823 | |||||||
| chr3:49084827 | A | T | 1 | a0001c0001t0001g0014 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-21-7789T>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49084827 | |||||||
| chr3:49085159 | T | C | 1 | a0001c0001t0002g0037 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-21-8121A>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49085159 | |||||||
| chr3:49085600 | C | CA | 4 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(1): Show |
4 | HG02145.hp1 HG02257.hp1 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.-22+8311dupT | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49085600 | |||||||
| chr3:49085629 | G | A | 1 | a0001c0001t0001g0028 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-22+8283C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49085629 | |||||||
| chr3:49085673 | G | A | 1 | a0001c0001t0001g0005 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-22+8239C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49085673 | |||||||
| chr3:49085879 | A | G | 4 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(1): Show |
4 | HG02145.hp1 HG02257.hp1 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.-22+8033T>C | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49085879 | |||||||
| chr3:49086133 | T | TA | 10 | a0001c0001t0001g0051 a0001c0001t0001g0071 a0001c0001t0001g0072 others(7): Show |
10 | HG02280.hp2 HG02559.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.-22+7778dupT | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49086133 | |||||||
| chr3:49086204 | G | A | 1 | a0001c0001t0001g0006 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-22+7708C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49086204 | |||||||
| chr3:49086261 | C | CT | 24 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0189 others(21): Show |
24 | HG00609.hp2 HG01074.hp2 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.-22+7650dupA | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49086261 | |||||||
| chr3:49086261 | CTTTTTTT others(6): Show |
C | 3 | a0001c0001t0001g0073 a0001c0001t0001g0150 a0001c0001t0001g0153 |
3 | HG02886.hp1 NA20300.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-22+7638_-22+7650d others(15): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49086261 | |||||||
| chr3:49086296 | G | A | 4 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 others(1): Show |
4 | NA18951.hp2 NA19000.hp1 NA19070.hp1 others(1): Show |
intron_variant | MODIFIER | c.-22+7616C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49086296 | |||||||
| chr3:49086326 | G | A | 3 | a0001c0001t0001g0016 a0001c0001t0001g0185 a0001c0001t0001g0186 |
3 | HG03490.hp2 HG03492.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-22+7586C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49086326 | |||||||
| chr3:49086469 | G | C | 1 | a0001c0001t0001g0005 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-22+7443C>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49086469 | |||||||
| chr3:49086470 | G | C | 1 | a0001c0001t0001g0005 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-22+7442C>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49086470 | |||||||
| chr3:49087013 | T | G | 1 | a0001c0001t0001g0029 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-22+6899A>C | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49087013 | |||||||
| chr3:49087150 | G | C | 2 | a0001c0001t0001g0013 a0001c0001t0001g0030 |
2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.-22+6762C>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49087150 | |||||||
| chr3:49087212 | G | A | 1 | a0001c0001t0001g0031 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-22+6700C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49087212 | |||||||
| chr3:49087213 | C | T | 2 | a0001c0001t0001g0092 a0001c0001t0001g0093 |
2 | NA18906.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-22+6699G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49087213 | |||||||
| chr3:49087384 | T | G | 31 | a0001c0001t0001g0038 a0001c0001t0001g0049 a0001c0001t0001g0050 others(28): Show |
32 | HG00544.hp2 HG00609.hp2 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.-22+6528A>C | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49087384 | |||||||
| chr3:49087470 | G | A | 1 | a0001c0001t0001g0070 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-22+6442C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49087470 | |||||||
| chr3:49087630 | C | T | 5 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0001g0087 others(2): Show |
5 | HG01070.hp2 HG01192.hp1 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.-22+6282G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49087630 | |||||||
| chr3:49087728 | G | A | 9 | a0001c0001t0001g0038 a0001c0001t0001g0049 a0001c0001t0001g0050 others(6): Show |
9 | HG00544.hp2 HG02280.hp2 HG02735.hp2 others(6): Show |
intron_variant | MODIFIER | c.-22+6184C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49087728 | |||||||
| chr3:49087818 | C | CA | 14 | a0001c0001t0001g0056 a0001c0001t0001g0062 a0001c0001t0001g0199 others(11): Show |
14 | HG01515.hp1 HG02486.hp2 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.-22+6093dupT | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49087818 | |||||||
| chr3:49087818 | C | CAA | 27 | a0001c0001t0001g0007 a0001c0001t0001g0049 a0001c0001t0001g0050 others(24): Show |
28 | HG00544.hp2 HG00609.hp2 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.-22+6092_-22+6093d others(4): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49087818 | |||||||
| chr3:49087818 | C | CAAAAAAA others(3): Show |
2 | a0001c0001t0001g0091 a0001c0001t0001g0184 |
2 | HG02280.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-22+6084_-22+6093d others(12): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49087818 | |||||||
| chr3:49087818 | C | CAAAAAAA others(4): Show |
21 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0066 others(18): Show |
21 | HG00140.hp2 HG00639.hp2 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.-22+6083_-22+6093d others(13): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49087818 | |||||||
| chr3:49087818 | C | CAAAAAAA others(5): Show |
35 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0098 others(32): Show |
35 | HG00738.hp1 HG00738.hp2 HG01168.hp2 others(32): Show |
intron_variant | MODIFIER | c.-22+6082_-22+6093d others(14): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49087818 | |||||||
| chr3:49087818 | C | CAAAAAAA others(6): Show |
34 | a0001c0001t0001g0059 a0001c0001t0001g0070 a0001c0001t0001g0075 others(31): Show |
34 | HG00280.hp2 HG00609.hp1 HG00735.hp1 others(31): Show |
intron_variant | MODIFIER | c.-22+6081_-22+6093d others(15): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49087818 | |||||||
| chr3:49087818 | C | CAAAAAAA others(7): Show |
24 | a0001c0001t0001g0008 a0001c0001t0001g0055 a0001c0001t0001g0076 others(21): Show |
24 | HG01074.hp1 HG01261.hp1 HG02129.hp2 others(21): Show |
intron_variant | MODIFIER | c.-22+6080_-22+6093d others(16): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49087818 | |||||||
| chr3:49087818 | C | CAAAAAAA others(8): Show |
7 | a0001c0001t0001g0090 a0001c0001t0001g0147 a0001c0001t0001g0156 others(4): Show |
7 | HG01981.hp1 HG01981.hp2 HG02074.hp2 others(4): Show |
intron_variant | MODIFIER | c.-22+6079_-22+6093d others(17): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49087818 | |||||||
| chr3:49087818 | C | CAAAAAAA others(9): Show |
4 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0164 others(1): Show |
4 | HG01192.hp2 HG01255.hp1 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.-22+6078_-22+6093d others(18): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49087818 | |||||||
| chr3:49087818 | C | CAAAAAAA others(10): Show |
1 | a0001c0001t0001g0071 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-22+6077_-22+6093d others(19): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49087818 | |||||||
| chr3:49087818 | C | CAAAAAAA others(11): Show |
3 | a0001c0001t0001g0072 a0001c0001t0001g0074 a0001c0001t0001g0148 |
3 | HG00544.hp1 HG02486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-22+6076_-22+6093d others(20): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49087818 | |||||||
| chr3:49087818 | C | CAAAAAAA others(12): Show |
3 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0153 |
3 | HG02886.hp1 HG06807.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-22+6075_-22+6093d others(21): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49087818 | |||||||
| chr3:49087818 | C | CAAAAAAA others(14): Show |
1 | a0001c0001t0001g0073 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-22+6073_-22+6093d others(23): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49087818 | |||||||
| chr3:49087842 | A | G | 1 | a0001c0001t0001g0166 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.-22+6070T>C | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49087842 | |||||||
| chr3:49087858 | T | G | 1 | a0001c0001t0001g0151 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-22+6054A>C | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49087858 | |||||||
| chr3:49087875 | A | G | 1 | a0001c0001t0003g0219 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-22+6037T>C | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49087875 | |||||||
| chr3:49087956 | AT | A | 5 | a0001c0001t0001g0032 a0001c0001t0001g0152 a0001c0001t0002g0004 others(2): Show |
5 | HG00733.hp1 HG03041.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.-22+5955delA | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49087956 | |||||||
| chr3:49088068 | C | A | 1 | a0001c0001t0001g0165 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-22+5844G>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49088068 | |||||||
| chr3:49088170 | C | G | 4 | a0001c0001t0001g0217 a0001c0001t0002g0004 a0001c0001t0002g0218 others(1): Show |
4 | HG03041.hp1 HG03453.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.-22+5742G>C | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49088170 | |||||||
| chr3:49088219 | G | C | 206 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(203): Show |
207 | HG00140.hp2 HG00280.hp2 HG00544.hp1 others(204): Show |
intron_variant | MODIFIER | c.-22+5693C>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49088219 | |||||||
| chr3:49088233 | G | A | 1 | a0001c0001t0001g0182 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-22+5679C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49088233 | |||||||
| chr3:49088262 | G | A | 3 | a0001c0001t0002g0004 a0001c0001t0002g0218 a0001c0004t0002g0003 |
3 | HG03041.hp1 HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-22+5650C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49088262 | |||||||
| chr3:49088440 | C | T | 5 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0001g0087 others(2): Show |
5 | HG01070.hp2 HG01192.hp1 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.-22+5472G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49088440 | |||||||
| chr3:49088618 | G | GT | 19 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(16): Show |
19 | HG00735.hp1 HG01070.hp2 HG01192.hp2 others(16): Show |
intron_variant | MODIFIER | c.-22+5293dupA | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49088618 | |||||||
| chr3:49088708 | C | T | 1 | a0001c0001t0001g0217 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-22+5204G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49088708 | |||||||
| chr3:49089041 | C | T | 4 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(1): Show |
4 | HG01243.hp1 HG02622.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.-22+4871G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49089041 | |||||||
| chr3:49089099 | C | T | 1 | a0001c0001t0001g0217 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-22+4813G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49089099 | |||||||
| chr3:49089308 | C | A | 1 | a0001c0001t0001g0184 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-22+4604G>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49089308 | |||||||
| chr3:49089368 | A | G | 1 | a0002c0002t0001g0011 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-22+4544T>C | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49089368 | |||||||
| chr3:49089409 | T | G | 1 | a0001c0001t0001g0153 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-22+4503A>C | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49089409 | |||||||
| chr3:49089421 | A | C | 2 | a0001c0001t0001g0075 a0001c0001t0001g0076 |
2 | NA18963.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.-22+4491T>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49089421 | |||||||
| chr3:49089817 | T | C | 4 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0156 others(1): Show |
4 | HG02109.hp1 HG02970.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.-22+4095A>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49089817 | |||||||
| chr3:49090197 | C | A | 1 | a0001c0001t0001g0005 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-22+3715G>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49090197 | |||||||
| chr3:49090197 | C | T | 1 | a0001c0001t0001g0158 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-22+3715G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49090197 | |||||||
| chr3:49090287 | G | A | 3 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0069 |
3 | NA19003.hp1 NA19012.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.-22+3625C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49090287 | |||||||
| chr3:49090453 | C | T | 1 | a0001c0001t0001g0074 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-22+3459G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49090453 | |||||||
| chr3:49090458 | C | CA | 134 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(131): Show |
134 | HG00140.hp2 HG00280.hp2 HG00544.hp1 others(131): Show |
intron_variant | MODIFIER | c.-22+3453dupT | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49090458 | |||||||
| chr3:49090458 | C | CAA | 9 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 others(6): Show |
9 | HG01981.hp1 HG02074.hp1 HG02602.hp2 others(6): Show |
intron_variant | MODIFIER | c.-22+3452_-22+3453d others(4): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49090458 | |||||||
| chr3:49090628 | C | CA | 110 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 others(107): Show |
110 | HG00140.hp2 HG00280.hp2 HG00544.hp1 others(107): Show |
intron_variant | MODIFIER | c.-22+3283dupT | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49090628 | |||||||
| chr3:49090628 | C | CAA | 21 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(18): Show |
21 | HG00639.hp2 HG00738.hp1 HG00738.hp2 others(18): Show |
intron_variant | MODIFIER | c.-22+3282_-22+3283d others(4): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49090628 | |||||||
| chr3:49090986 | G | A | 1 | a0001c0001t0001g0184 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-22+2926C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49090986 | |||||||
| chr3:49091810 | G | A | 2 | a0001c0001t0001g0185 a0001c0001t0001g0186 |
2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-22+2102C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49091810 | |||||||
| chr3:49092148 | G | T | 3 | a0001c0001t0002g0004 a0001c0001t0002g0218 a0001c0004t0002g0003 |
3 | HG03041.hp1 HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-22+1764C>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49092148 | |||||||
| chr3:49092192 | T | C | 21 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0189 others(18): Show |
21 | HG01074.hp2 HG01243.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.-22+1720A>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49092192 | |||||||
| chr3:49092230 | G | A | 1 | a0001c0001t0001g0208 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-22+1682C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49092230 | |||||||
| chr3:49092381 | A | G | 2 | a0001c0001t0001g0009 a0001c0001t0001g0010 |
2 | HG00639.hp2 HG01256.hp2 |
intron_variant | MODIFIER | c.-22+1531T>C | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49092381 | |||||||
| chr3:49092626 | G | A | 3 | a0001c0001t0002g0004 a0001c0001t0002g0218 a0001c0004t0002g0003 |
3 | HG03041.hp1 HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-22+1286C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49092626 | |||||||
| chr3:49092642 | C | T | 1 | a0001c0001t0001g0008 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-22+1270G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49092642 | |||||||
| chr3:49092682 | A | G | 1 | a0001c0001t0001g0217 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-22+1230T>C | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49092682 | |||||||
| chr3:49092691 | GAACA | G | 2 | a0001c0001t0001g0006 a0001c0001t0001g0007 |
2 | HG01884.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.-22+1217_-22+1220d others(6): Show |
QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49092691 | |||||||
| chr3:49092833 | A | G | 1 | a0001c0001t0001g0209 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-22+1079T>C | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49092833 | |||||||
| chr3:49092841 | A | G | 1 | a0001c0001t0001g0005 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-22+1071T>C | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49092841 | |||||||
| chr3:49092917 | T | C | 1 | a0001c0001t0001g0209 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-22+995A>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49092917 | |||||||
| chr3:49092945 | T | C | 7 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0212 others(4): Show |
7 | HG00140.hp2 HG00280.hp2 HG01516.hp1 others(4): Show |
intron_variant | MODIFIER | c.-22+967A>G | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49092945 | |||||||
| chr3:49093165 | G | A | 1 | a0001c0001t0001g0217 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-22+747C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49093165 | |||||||
| chr3:49093305 | C | G | 3 | a0001c0001t0002g0004 a0001c0001t0002g0218 a0001c0004t0002g0003 |
3 | HG03041.hp1 HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-22+607G>C | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49093305 | |||||||
| chr3:49093820 | G | A | 1 | a0001c0001t0002g0218 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-22+92C>T | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49093820 | |||||||
| chr3:49093871 | C | T | 1 | a0001c0001t0001g0002 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-22+41G>A | QRICH1 | ENSG00000198218.12 | transcript | ENST00000395443.7 | protein_coding | 1/9 | chr3 | 49093871 |