Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 5971 |
| ensemblid | ENSG00000104856.15 |
| hgncid | 9956 |
| symbol | RELB |
| name | RELB proto-oncogene, NF-kB subunit |
| refseq_nuc | NM_006509.4 |
| refseq_prot | NP_006500.2 |
| ensembl_nuc | ENST00000221452.13 |
| ensembl_prot | ENSP00000221452.7 |
| mane_status | MANE Select |
| chr | chr19 |
| start | 45001464 |
| end | 45038192 |
| strand | + |
| ver | v1.2 |
| region | chr19:45001464-45038192 |
| region5000 | chr19:44996464-45043192 |
| regionname0 | RELB_chr19_45001464_45038192 |
| regionname5000 | RELB_chr19_44996464_45043192 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 579 | 381 | 96 | 74 | 151 | 12 | 46 | 110 | RELB_chr19_44996464_45043192 | RELB | MLRSG others(574): Show |
chr19 | 44996464 | 45043192 |
| a0002 | 0/0 | 579 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | MLRSG others(574): Show |
chr19 | 44996464 | 45043192 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1737 | 373 | 91 | 74 | 149 | 12 | 45 | RELB_chr19_44996464_45043192 | RELB | ATGCT others(1732): Show |
chr19 | 44996464 | 45043192 | ||
| a0001c0002 | 0/0 | 1737 | 4 | 4 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | ATGCT others(1732): Show |
chr19 | 44996464 | 45043192 | ||
| a0001c0003 | 0/0 | 1737 | 1 | 0 | 0 | 0 | 0 | 1 | RELB_chr19_44996464_45043192 | RELB | ATGCT others(1732): Show |
chr19 | 44996464 | 45043192 | ||
| a0001c0004 | 0/0 | 1737 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | ATGCT others(1732): Show |
chr19 | 44996464 | 45043192 | ||
| a0001c0005 | 0/0 | 1737 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | ATGCT others(1732): Show |
chr19 | 44996464 | 45043192 | ||
| a0001c0006 | 0/0 | 1737 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | ATGCT others(1732): Show |
chr19 | 44996464 | 45043192 | ||
| a0002c0007 | 0/0 | 1737 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | ATGCT others(1732): Show |
chr19 | 44996464 | 45043192 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2258 | 348 | 91 | 69 | 136 | 10 | 40 | RELB_chr19_44996464_45043192 | RELB | GCAGC others(2253): Show |
chr19 | 44996464 | 45043192 |
| a0001c0001t0002 | 0/0 | 2258 | 16 | 0 | 0 | 12 | 0 | 4 | RELB_chr19_44996464_45043192 | RELB | GCAGC others(2253): Show |
chr19 | 44996464 | 45043192 |
| a0001c0001t0003 | 0/0 | 2258 | 7 | 0 | 5 | 0 | 2 | 0 | RELB_chr19_44996464_45043192 | RELB | GCAGC others(2253): Show |
chr19 | 44996464 | 45043192 |
| a0001c0001t0004 | 0/0 | 2258 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | GCAGC others(2253): Show |
chr19 | 44996464 | 45043192 |
| a0001c0001t0005 | 0/0 | 2258 | 1 | 0 | 0 | 0 | 0 | 1 | RELB_chr19_44996464_45043192 | RELB | GCAGC others(2253): Show |
chr19 | 44996464 | 45043192 |
| a0001c0002t0001 | 0/0 | 2258 | 4 | 4 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | GCAGC others(2253): Show |
chr19 | 44996464 | 45043192 |
| a0001c0003t0001 | 0/0 | 2258 | 1 | 0 | 0 | 0 | 0 | 1 | RELB_chr19_44996464_45043192 | RELB | GCAGC others(2253): Show |
chr19 | 44996464 | 45043192 |
| a0001c0004t0001 | 0/0 | 2258 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | GCAGC others(2253): Show |
chr19 | 44996464 | 45043192 |
| a0001c0005t0001 | 0/0 | 2258 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | GCAGC others(2253): Show |
chr19 | 44996464 | 45043192 |
| a0001c0006t0002 | 0/0 | 2258 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | GCAGC others(2253): Show |
chr19 | 44996464 | 45043192 |
| a0002c0007t0001 | 0/0 | 2258 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | GCAGC others(2253): Show |
chr19 | 44996464 | 45043192 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0056 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0277 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0351 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0369 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0370 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0372 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0373 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0001g0374 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0002g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0002g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0002g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0002g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0003g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0003g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0003g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0003g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0003g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0003g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0003g0271 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0004g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0001t0005g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0002t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0002t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0002t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0002t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0003t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0004t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0005t0001g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0001c0006t0002g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| a0002c0007t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0147 | EUR | GBR | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0094 | EUR | GBR | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0257 | EUR | GBR | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0044 | EUR | GBR | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0061 | EUR | FIN | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0242 | EUR | FIN | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0319 | EAS | CHS | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | CHS | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | CHS | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG00423 | hp2 | a0002 | c0007 | t0001 | g0236 | EAS | CHS | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | CHS | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | CHS | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | CHS | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | CHS | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | CHS | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | CHS | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | CHS | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | CHS | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | CHS | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | CHS | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | CHS | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0366 | EAS | CHS | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0224 | AMR | PUR | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0213 | AMR | PUR | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | CHS | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | CHS | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0308 | AMR | PUR | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0313 | AMR | PUR | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0181 | AMR | PUR | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0228 | AMR | PUR | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0324 | AMR | PUR | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0221 | AMR | PUR | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0321 | AMR | PUR | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | PUR | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0064 | AMR | PUR | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG01081 | hp1 | a0001 | c0001 | t0003 | g0256 | AMR | PUR | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0148 | AMR | PUR | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0199 | AMR | PUR | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0342 | AMR | PUR | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0167 | AMR | PUR | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0162 | AMR | PUR | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0211 | AMR | PUR | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG01192 | hp2 | a0001 | c0001 | t0003 | g0010 | AMR | PUR | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0369 | AMR | PUR | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | PUR | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0252 | AMR | CLM | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG01255 | hp2 | a0001 | c0001 | t0003 | g0011 | AMR | CLM | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | CLM | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0244 | AMR | CLM | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | CLM | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | CLM | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG01346 | hp1 | a0001 | c0001 | t0003 | g0189 | AMR | CLM | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0168 | AMR | CLM | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0370 | AMR | CLM | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0320 | AMR | CLM | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0296 | AMR | CLM | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG01361 | hp2 | a0001 | c0001 | t0003 | g0245 | AMR | CLM | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0053 | AMR | CLM | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0307 | AMR | CLM | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0219 | AMR | CLM | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | CLM | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0246 | EUR | IBS | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0302 | EUR | IBS | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG01516 | hp2 | a0001 | c0001 | t0003 | g0271 | EUR | IBS | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0090 | EUR | IBS | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG01517 | hp2 | a0001 | c0001 | t0003 | g0230 | EUR | IBS | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | ACB | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0207 | AFR | ACB | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | ACB | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0316 | AFR | ACB | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0341 | AMR | PEL | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0285 | AMR | PEL | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | PEL | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0323 | AMR | PEL | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PEL | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0214 | AMR | PEL | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | PEL | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0309 | AMR | PEL | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PEL | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0047 | AMR | PEL | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0346 | AMR | PEL | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | PEL | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0268 | AMR | PEL | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | PEL | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | KHV | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0371 | EAS | KHV | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | KHV | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | KHV | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0311 | AFR | ACB | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0352 | AFR | ACB | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | KHV | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0348 | EAS | KHV | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | KHV | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | KHV | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | KHV | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0328 | EAS | KHV | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | KHV | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | KHV | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | KHV | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | KHV | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | KHV | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | KHV | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | ACB | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0208 | AFR | ACB | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0344 | AMR | PEL | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0304 | EAS | CDX | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | CDX | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0359 | AFR | ACB | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0372 | AFR | ACB | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0362 | AFR | ACB | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0306 | AFR | ACB | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0062 | AMR | PEL | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0356 | AFR | ACB | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0315 | AFR | ACB | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0283 | AMR | PEL | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PEL | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | PEL | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PEL | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0275 | AFR | ACB | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG02451 | hp2 | a0001 | c0002 | t0001 | g0133 | AFR | ACB | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0335 | EAS | KHV | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0151 | EAS | KHV | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0318 | AFR | GWD | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | GWD | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0068 | SAS | PJL | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0067 | SAS | PJL | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | GWD | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | GWD | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | GWD | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | GWD | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0361 | AFR | GWD | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0239 | AFR | GWD | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | GWD | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | GWD | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0152 | SAS | PJL | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0084 | SAS | PJL | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0357 | AFR | GWD | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | GWD | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | GWD | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0272 | AFR | GWD | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0351 | SAS | PJL | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0154 | SAS | PJL | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0034 | SAS | PJL | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | GWD | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | GWD | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | GWD | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0358 | AFR | GWD | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | GWD | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | GWD | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | GWD | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | GWD | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | GWD | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0273 | AFR | ESN | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | ESN | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | ESN | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | ESN | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0274 | AFR | ESN | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | ESN | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0250 | SAS | PJL | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG03017 | hp2 | a0001 | c0001 | t0005 | g0183 | SAS | PJL | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0270 | AFR | GWD | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | GWD | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | MSL | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG03098 | hp2 | a0001 | c0002 | t0001 | g0140 | AFR | MSL | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | ESN | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0373 | AFR | ESN | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | ESN | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0317 | AFR | ESN | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0225 | AFR | ESN | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | ESN | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | MSL | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | MSL | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | MSL | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | MSL | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0269 | SAS | PJL | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0186 | SAS | PJL | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0276 | AFR | MSL | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0367 | AFR | MSL | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | MSL | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | MSL | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0040 | SAS | PJL | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0280 | SAS | PJL | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0329 | SAS | PJL | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0204 | AFR | ESN | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0360 | AFR | ESN | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0206 | AFR | GWD | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG03540 | hp2 | a0001 | c0002 | t0001 | g0104 | AFR | GWD | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | MSL | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | MSL | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0262 | SAS | PJL | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG03654 | hp2 | a0001 | c0003 | t0001 | g0253 | SAS | PJL | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0074 | SAS | PJL | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0103 | SAS | STU | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0071 | SAS | STU | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0163 | SAS | PJL | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0058 | SAS | PJL | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0243 | SAS | PJL | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0231 | SAS | BEB | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0126 | SAS | BEB | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0212 | SAS | BEB | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0222 | SAS | BEB | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0150 | SAS | BEB | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0156 | SAS | BEB | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0049 | SAS | STU | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0043 | SAS | STU | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0294 | SAS | BEB | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0310 | SAS | BEB | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0091 | SAS | STU | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0116 | SAS | STU | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0045 | SAS | STU | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0107 | SAS | STU | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0209 | SAS | STU | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0303 | SAS | STU | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0202 | AFR | YRI | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | YRI | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | CHB | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | CHB | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0334 | EAS | CHB | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | CHB | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0325 | AFR | YRI | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0368 | AFR | YRI | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0337 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0330 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0327 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0350 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0339 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0332 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0349 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0340 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0364 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0333 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0326 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0338 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0251 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0196 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0363 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0365 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0336 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0226 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| NA19000 | hp1 | a0001 | c0005 | t0001 | g0345 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| NA19004 | hp2 | a0001 | c0006 | t0002 | g0322 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0295 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | LWK | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | LWK | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | LWK | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | LWK | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0109 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0117 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0331 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0347 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| NA19079 | hp1 | a0001 | c0001 | t0004 | g0201 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0343 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0355 | AFR | ASW | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0235 | AFR | ASW | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0066 | SAS | GIH | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0055 | SAS | GIH | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0354 | AMR | CLM | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | CLM | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0374 | AFR | ACB | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG02109 | hp2 | a0001 | c0002 | t0001 | g0131 | AFR | ACB | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0353 | AFR | ACB | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0312 | AFR | ACB | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | ACB | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0297 | AFR | ACB | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | MSL | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | MSL | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | USA | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | USA | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| NA20300 | hp1 | a0001 | c0004 | t0001 | g0241 | AFR | USA | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | USA | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0282 | AFR | LWK | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | LWK | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0277 | REF | REF | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0056 | REF | REF | RELB_chr19_44996464_45043192 | RELB | chr19 | 44996464 | 45043192 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:45011996 | C | G | 1 | a0002 | 1 | HG00423.hp2 | missense_variant | MODERATE | c.224C>G | p.Pro75Arg | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/12 | 340/2258 | 224/1740 | 75/579 | chr19 | 45011996 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:45001636 | G | C | 1 | a0001c0003 | 1 | HG03654.hp2 | synonymous_variant | LOW | c.57G>C | p.Pro19Pro | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 1/12 | 173/2258 | 57/1740 | 19/579 | chr19 | 45001636 | |||
| chr19:45012177 | G | A | 1 | a0001c0004 | 1 | NA20300.hp1 | synonymous_variant | LOW | c.405G>A | p.Gln135Gln | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/12 | 521/2258 | 405/1740 | 135/579 | chr19 | 45012177 | |||
| chr19:45032640 | C | T | 1 | a0001c0006 | 1 | NA19004.hp2 | synonymous_variant | LOW | c.1098C>T | p.Tyr366Tyr | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 9/12 | 1214/2258 | 1098/1740 | 366/579 | chr19 | 45032640 | |||
| chr19:45037508 | C | T | 1 | a0001c0002 | 4 | HG02109.hp2 HG02451.hp2 HG03098.hp2 others(1): Show |
synonymous_variant | LOW | c.1458C>T | p.Asp486Asp | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 12/12 | 1574/2258 | 1458/1740 | 486/579 | chr19 | 45037508 | |||
| chr19:45037667 | C | T | 1 | a0001c0005 | 1 | NA19000.hp1 | synonymous_variant | LOW | c.1617C>T | p.Tyr539Tyr | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 12/12 | 1733/2258 | 1617/1740 | 539/579 | chr19 | 45037667 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:45038070 | G | A | 1 | a0001c0001t0004 | 1 | NA19079.hp1 | 3_prime_UTR_variant | MODIFIER | c.*280G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 12/12 | 280 | chr19 | 45038070 | ||||||
| chr19:45038120 | C | T | 1 | a0001c0001t0005 | 1 | HG03017.hp2 | 3_prime_UTR_variant | MODIFIER | c.*330C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 12/12 | 330 | chr19 | 45038120 | ||||||
| chr19:45038140 | G | T | 2 | a0001c0001t0002 a0001c0006t0002 |
17 | HG02080.hp2 HG02523.hp2 HG02602.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*350G>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 12/12 | 350 | chr19 | 45038140 | ||||||
| chr19:45038156 | G | T | 1 | a0001c0001t0003 | 7 | HG01081.hp1 HG01192.hp2 HG01255.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*366G>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 12/12 | 366 | chr19 | 45038156 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:45001765 | G | T | 2 | a0001c0001t0001g0373 a0001c0001t0001g0374 |
2 | HG02109.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.106+80G>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 1/11 | chr19 | 45001765 | |||||||
| chr19:45001884 | G | C | 1 | a0001c0001t0001g0009 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.106+199G>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 1/11 | chr19 | 45001884 | |||||||
| chr19:45001919 | C | A | 3 | a0001c0001t0001g0012 a0001c0001t0003g0010 a0001c0001t0003g0011 |
3 | HG01192.hp2 HG01255.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.106+234C>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 1/11 | chr19 | 45001919 | |||||||
| chr19:45002058 | C | T | 1 | a0001c0001t0001g0372 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.106+373C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 1/11 | chr19 | 45002058 | |||||||
| chr19:45002059 | C | G | 1 | a0001c0001t0001g0371 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.106+374C>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 1/11 | chr19 | 45002059 | |||||||
| chr19:45002077 | G | A | 1 | a0001c0001t0001g0013 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.106+392G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 1/11 | chr19 | 45002077 | |||||||
| chr19:45002090 | T | C | 2 | a0001c0001t0001g0014 a0001c0001t0001g0015 |
2 | HG00735.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.106+405T>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 1/11 | chr19 | 45002090 | |||||||
| chr19:45002126 | G | T | 1 | a0001c0001t0001g0370 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.106+441G>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 1/11 | chr19 | 45002126 | |||||||
| chr19:45002163 | A | C | 3 | a0001c0001t0001g0367 a0001c0001t0001g0368 a0001c0001t0001g0369 |
3 | HG01243.hp1 HG03453.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.106+478A>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 1/11 | chr19 | 45002163 | |||||||
| chr19:45002169 | A | G | 4 | a0001c0001t0001g0364 a0001c0001t0001g0365 a0001c0001t0001g0366 others(1): Show |
4 | HG00621.hp2 NA18962.hp1 NA18977.hp1 others(1): Show |
intron_variant | MODIFIER | c.106+484A>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 1/11 | chr19 | 45002169 | |||||||
| chr19:45002184 | C | A | 10 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(7): Show |
10 | HG01943.hp1 HG01981.hp1 HG02148.hp1 others(7): Show |
intron_variant | MODIFIER | c.106+499C>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 1/11 | chr19 | 45002184 | |||||||
| chr19:45002307 | T | C | 1 | a0001c0001t0001g0026 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.106+622T>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 1/11 | chr19 | 45002307 | |||||||
| chr19:45002338 | T | G | 2 | a0001c0001t0001g0027 a0001c0001t0001g0028 |
2 | NA19009.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.107-611T>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 1/11 | chr19 | 45002338 | |||||||
| chr19:45002407 | C | G | 7 | a0001c0001t0001g0356 a0001c0001t0001g0357 a0001c0001t0001g0358 others(4): Show |
7 | HG02257.hp1 HG02258.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.107-542C>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 1/11 | chr19 | 45002407 | |||||||
| chr19:45002411 | G | A | 1 | a0001c0001t0001g0029 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.107-538G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 1/11 | chr19 | 45002411 | |||||||
| chr19:45002446 | G | A | 1 | a0001c0001t0001g0030 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.107-503G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 1/11 | chr19 | 45002446 | |||||||
| chr19:45002519 | A | T | 4 | a0001c0001t0001g0352 a0001c0001t0001g0353 a0001c0001t0001g0354 others(1): Show |
4 | HG01123.hp1 HG02055.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.107-430A>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 1/11 | chr19 | 45002519 | |||||||
| chr19:45002545 | G | C | 11 | a0001c0001t0001g0009 a0001c0001t0001g0031 a0001c0001t0001g0032 others(8): Show |
11 | HG00597.hp2 HG02135.hp2 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.107-404G>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 1/11 | chr19 | 45002545 | |||||||
| chr19:45002651 | C | A | 1 | a0001c0001t0001g0041 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.107-298C>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 1/11 | chr19 | 45002651 | |||||||
| chr19:45003147 | C | T | 1 | a0001c0001t0001g0351 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.154+151C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45003147 | |||||||
| chr19:45003171 | T | G | 1 | a0001c0001t0001g0042 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.154+175T>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45003171 | |||||||
| chr19:45003287 | C | T | 1 | a0001c0001t0001g0040 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.154+291C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45003287 | |||||||
| chr19:45003368 | G | T | 1 | a0001c0001t0001g0039 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.154+372G>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45003368 | |||||||
| chr19:45003424 | G | A | 3 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 |
3 | HG00597.hp2 HG02135.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.154+428G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45003424 | |||||||
| chr19:45003441 | C | G | 1 | a0001c0001t0001g0350 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.154+445C>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45003441 | |||||||
| chr19:45003474 | C | CA | 10 | a0001c0001t0001g0026 a0001c0001t0001g0044 a0001c0001t0001g0045 others(7): Show |
10 | HG00140.hp2 HG01952.hp1 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.154+503dupA | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 45003474 | ||||||
| chr19:45003474 | CA | C | 13 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0077 others(10): Show |
13 | HG00609.hp1 HG01109.hp2 HG01981.hp1 others(10): Show |
intron_variant | MODIFIER | c.154+503delA | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 45003474 | ||||||
| chr19:45003474 | CAA | C | 56 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0019 others(53): Show |
58 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.154+502_154+503del others(2): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 45003474 | ||||||
| chr19:45003474 | CAAA | C | 234 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(231): Show |
238 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(235): Show |
intron_variant | MODIFIER | c.154+501_154+503del others(3): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 45003474 | ||||||
| chr19:45003474 | CAAAA | C | 29 | a0001c0001t0001g0008 a0001c0001t0001g0041 a0001c0001t0001g0042 others(26): Show |
30 | HG00738.hp2 HG01109.hp1 HG01928.hp1 others(27): Show |
intron_variant | MODIFIER | c.154+500_154+503del others(4): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 45003474 | ||||||
| chr19:45003514 | T | A | 332 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(329): Show |
339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.154+518T>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45003514 | |||||||
| chr19:45003549 | A | G | 9 | a0001c0001t0001g0087 a0001c0001t0001g0352 a0001c0001t0001g0353 others(6): Show |
9 | HG01123.hp1 HG01243.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.154+553A>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45003549 | |||||||
| chr19:45003567 | T | C | 13 | a0001c0001t0001g0041 a0001c0001t0001g0087 a0001c0001t0001g0128 others(10): Show |
13 | HG00738.hp2 HG01123.hp1 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.154+571T>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45003567 | |||||||
| chr19:45003890 | T | G | 1 | a0001c0001t0001g0129 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.154+894T>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45003890 | |||||||
| chr19:45003893 | G | GT | 5 | a0001c0001t0001g0013 a0001c0001t0001g0050 a0001c0001t0001g0075 others(2): Show |
5 | HG01934.hp2 HG02300.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.154+905dupT | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 45003893 | ||||||
| chr19:45003913 | G | T | 5 | a0001c0001t0001g0352 a0001c0001t0001g0353 a0001c0001t0001g0354 others(2): Show |
5 | HG01123.hp1 HG02055.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.154+917G>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45003913 | |||||||
| chr19:45003915 | G | GT | 82 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0046 others(79): Show |
84 | HG00099.hp1 HG00544.hp1 HG00544.hp2 others(81): Show |
intron_variant | MODIFIER | c.154+945dupT | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 45003915 | ||||||
| chr19:45003915 | G | GTT | 57 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0015 others(54): Show |
58 | HG00438.hp1 HG00597.hp1 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.154+944_154+945dup others(2): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 45003915 | ||||||
| chr19:45003915 | G | GTTT | 77 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(74): Show |
80 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.154+943_154+945dup others(3): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 45003915 | ||||||
| chr19:45003915 | G | GTTTT | 56 | a0001c0001t0001g0030 a0001c0001t0001g0085 a0001c0001t0001g0121 others(53): Show |
56 | HG00408.hp1 HG00438.hp2 HG00673.hp1 others(53): Show |
intron_variant | MODIFIER | c.154+942_154+945dup others(4): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 45003915 | ||||||
| chr19:45003915 | G | T | 7 | a0001c0001t0001g0352 a0001c0001t0001g0353 a0001c0001t0001g0354 others(4): Show |
7 | HG01123.hp1 HG01243.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.154+919G>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45003915 | |||||||
| chr19:45003915 | GTTTT | G | 10 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0034 others(7): Show |
10 | HG00609.hp1 HG01109.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.154+942_154+945del others(4): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 45003915 | ||||||
| chr19:45003915 | GTTTTT | G | 47 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(44): Show |
49 | HG00099.hp2 HG00597.hp2 HG01099.hp2 others(46): Show |
intron_variant | MODIFIER | c.154+941_154+945del others(5): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 45003915 | ||||||
| chr19:45004244 | C | T | 2 | a0001c0001t0001g0368 a0001c0001t0001g0369 |
2 | HG01243.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.154+1248C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45004244 | |||||||
| chr19:45004284 | G | A | 16 | a0001c0001t0001g0009 a0001c0001t0001g0031 a0001c0001t0001g0032 others(13): Show |
16 | HG00597.hp2 HG02109.hp2 HG02135.hp2 others(13): Show |
intron_variant | MODIFIER | c.154+1288G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45004284 | |||||||
| chr19:45004322 | G | A | 1 | a0001c0001t0001g0367 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.154+1326G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45004322 | |||||||
| chr19:45004413 | A | G | 30 | a0001c0001t0001g0009 a0001c0001t0001g0031 a0001c0001t0001g0032 others(27): Show |
30 | HG00597.hp2 HG00738.hp2 HG01123.hp1 others(27): Show |
intron_variant | MODIFIER | c.154+1417A>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45004413 | |||||||
| chr19:45004423 | C | T | 1 | a0001c0006t0002g0322 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.154+1427C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45004423 | |||||||
| chr19:45004438 | G | A | 1 | a0001c0001t0001g0147 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.154+1442G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45004438 | |||||||
| chr19:45004503 | C | T | 1 | a0001c0001t0001g0372 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.154+1507C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45004503 | |||||||
| chr19:45004557 | C | A | 5 | a0001c0001t0001g0121 a0001c0001t0001g0232 a0001c0001t0001g0233 others(2): Show |
5 | HG00408.hp2 HG02080.hp1 HG02132.hp1 others(2): Show |
intron_variant | MODIFIER | c.154+1561C>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45004557 | |||||||
| chr19:45004617 | C | T | 1 | a0001c0001t0001g0129 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.154+1621C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45004617 | |||||||
| chr19:45004697 | A | G | 14 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0087 others(11): Show |
14 | HG00738.hp2 HG01123.hp1 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.154+1701A>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45004697 | |||||||
| chr19:45004823 | T | C | 5 | a0001c0001t0001g0130 a0001c0001t0001g0132 a0001c0002t0001g0131 others(2): Show |
5 | HG02109.hp2 HG02451.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.154+1827T>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45004823 | |||||||
| chr19:45004892 | G | A | 1 | a0001c0001t0001g0087 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.154+1896G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45004892 | |||||||
| chr19:45004935 | C | G | 1 | a0001c0001t0001g0120 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.154+1939C>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45004935 | |||||||
| chr19:45005014 | A | C | 50 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(47): Show |
52 | HG00099.hp2 HG00609.hp1 HG01074.hp2 others(49): Show |
intron_variant | MODIFIER | c.154+2018A>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45005014 | |||||||
| chr19:45005026 | C | T | 2 | a0001c0001t0001g0045 a0001c0001t0001g0049 |
2 | HG04115.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.154+2030C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45005026 | |||||||
| chr19:45005031 | C | T | 1 | a0001c0001t0001g0372 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.154+2035C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45005031 | |||||||
| chr19:45005087 | C | T | 42 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0016 others(39): Show |
44 | HG00099.hp2 HG00609.hp1 HG01099.hp2 others(41): Show |
intron_variant | MODIFIER | c.154+2091C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45005087 | |||||||
| chr19:45005093 | C | T | 2 | a0001c0001t0001g0231 a0001c0001t0001g0323 |
2 | HG01934.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.154+2097C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45005093 | |||||||
| chr19:45005123 | A | T | 1 | a0001c0001t0001g0285 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.154+2127A>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45005123 | |||||||
| chr19:45005154 | G | C | 1 | a0001c0001t0001g0130 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.154+2158G>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45005154 | |||||||
| chr19:45005156 | G | A | 1 | a0001c0001t0001g0042 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.154+2160G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45005156 | |||||||
| chr19:45005264 | G | A | 1 | a0001c0001t0001g0029 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.154+2268G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45005264 | |||||||
| chr19:45005296 | T | C | 3 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 |
3 | HG02717.hp2 HG03195.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.154+2300T>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45005296 | |||||||
| chr19:45005439 | G | T | 5 | a0001c0001t0001g0130 a0001c0001t0001g0132 a0001c0002t0001g0131 others(2): Show |
5 | HG02109.hp2 HG02451.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.154+2443G>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45005439 | |||||||
| chr19:45005589 | C | G | 155 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(152): Show |
159 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.154+2593C>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45005589 | |||||||
| chr19:45005613 | C | CT | 8 | a0001c0001t0001g0007 a0001c0001t0001g0080 a0001c0001t0001g0085 others(5): Show |
9 | HG00438.hp2 HG01069.hp1 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.154+2625dupT | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 45005613 | ||||||
| chr19:45005766 | C | A | 331 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(328): Show |
338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.154+2770C>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45005766 | |||||||
| chr19:45005773 | T | C | 1 | a0001c0001t0001g0051 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.154+2777T>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45005773 | |||||||
| chr19:45005792 | C | T | 2 | a0001c0001t0001g0033 a0001c0001t0001g0198 |
2 | HG00558.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.154+2796C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45005792 | |||||||
| chr19:45006244 | G | A | 4 | a0001c0001t0001g0352 a0001c0001t0001g0353 a0001c0001t0001g0354 others(1): Show |
4 | HG01123.hp1 HG02055.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.154+3248G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45006244 | |||||||
| chr19:45006446 | C | G | 1 | a0001c0001t0001g0066 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.155-3368C>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45006446 | |||||||
| chr19:45006502 | C | T | 8 | a0001c0001t0001g0079 a0001c0001t0001g0082 a0001c0001t0001g0134 others(5): Show |
8 | HG01099.hp2 HG01109.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.155-3312C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45006502 | |||||||
| chr19:45006683 | G | C | 1 | a0001c0001t0001g0087 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.155-3131G>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45006683 | |||||||
| chr19:45006696 | C | T | 1 | a0001c0001t0001g0197 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.155-3118C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45006696 | |||||||
| chr19:45006714 | A | G | 5 | a0001c0001t0001g0195 a0001c0001t0001g0227 a0001c0001t0002g0109 others(2): Show |
5 | NA18950.hp2 NA18973.hp1 NA18999.hp2 others(2): Show |
intron_variant | MODIFIER | c.155-3100A>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45006714 | |||||||
| chr19:45006800 | A | G | 1 | a0001c0001t0001g0031 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.155-3014A>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45006800 | |||||||
| chr19:45006822 | G | A | 1 | a0001c0001t0001g0235 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.155-2992G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45006822 | |||||||
| chr19:45006832 | G | T | 1 | a0001c0001t0001g0235 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.155-2982G>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45006832 | |||||||
| chr19:45006834 | A | T | 1 | a0001c0001t0001g0235 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.155-2980A>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45006834 | |||||||
| chr19:45006836 | T | G | 1 | a0001c0001t0001g0235 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.155-2978T>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45006836 | |||||||
| chr19:45006837 | C | T | 1 | a0001c0001t0001g0235 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.155-2977C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45006837 | |||||||
| chr19:45006838 | C | A | 1 | a0001c0001t0001g0235 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.155-2976C>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45006838 | |||||||
| chr19:45006839 | C | G | 1 | a0001c0001t0001g0235 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.155-2975C>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45006839 | |||||||
| chr19:45006847 | C | A | 1 | a0001c0001t0001g0235 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.155-2967C>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45006847 | |||||||
| chr19:45006955 | GA | G | 8 | a0001c0001t0001g0129 a0001c0001t0001g0139 a0001c0001t0001g0147 others(5): Show |
8 | HG00099.hp1 HG02897.hp1 HG03491.hp1 others(5): Show |
intron_variant | MODIFIER | c.155-2842delA | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 45006955 | ||||||
| chr19:45007154 | C | T | 1 | a0001c0001t0001g0320 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.155-2660C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45007154 | |||||||
| chr19:45007268 | TA | T | 14 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0100 others(11): Show |
14 | HG00408.hp1 HG01175.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.155-2543delA | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 45007268 | ||||||
| chr19:45007368 | C | T | 1 | a0001c0001t0001g0282 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.155-2446C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45007368 | |||||||
| chr19:45007631 | G | A | 1 | a0002c0007t0001g0236 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.155-2183G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45007631 | |||||||
| chr19:45007687 | G | A | 1 | a0001c0001t0001g0148 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.155-2127G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45007687 | |||||||
| chr19:45007762 | G | A | 1 | a0001c0001t0001g0088 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.155-2052G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45007762 | |||||||
| chr19:45007773 | G | A | 4 | a0001c0001t0001g0130 a0001c0002t0001g0131 a0001c0002t0001g0133 others(1): Show |
4 | HG02109.hp2 HG02451.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.155-2041G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45007773 | |||||||
| chr19:45007783 | G | A | 1 | a0001c0001t0002g0330 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.155-2031G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45007783 | |||||||
| chr19:45007783 | G | T | 1 | a0001c0001t0001g0126 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.155-2031G>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45007783 | |||||||
| chr19:45007816 | CCA | C | 93 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0027 others(90): Show |
93 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.155-1994_155-1993d others(4): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 45007816 | ||||||
| chr19:45007882 | C | A | 90 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0027 others(87): Show |
90 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.155-1932C>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45007882 | |||||||
| chr19:45008000 | C | CA | 31 | a0001c0001t0001g0013 a0001c0001t0001g0023 a0001c0001t0001g0031 others(28): Show |
31 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(28): Show |
intron_variant | MODIFIER | c.155-1791dupA | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 45008000 | ||||||
| chr19:45008000 | CA | C | 163 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(160): Show |
165 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.155-1791delA | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 45008000 | ||||||
| chr19:45008000 | CAA | C | 22 | a0001c0001t0001g0034 a0001c0001t0001g0036 a0001c0001t0001g0037 others(19): Show |
22 | HG01256.hp2 HG02055.hp1 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.155-1792_155-1791d others(4): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 45008000 | ||||||
| chr19:45008018 | A | G | 8 | a0001c0001t0001g0009 a0001c0001t0001g0123 a0001c0001t0001g0160 others(5): Show |
8 | HG00733.hp2 HG01884.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.155-1796A>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45008018 | |||||||
| chr19:45008036 | G | A | 2 | a0001c0001t0001g0141 a0001c0001t0001g0142 |
2 | HG02896.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.155-1778G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45008036 | |||||||
| chr19:45008165 | G | A | 1 | a0001c0001t0001g0302 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.155-1649G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45008165 | |||||||
| chr19:45008186 | A | G | 3 | a0001c0001t0001g0268 a0001c0001t0001g0285 a0001c0001t0001g0309 |
3 | HG01928.hp2 HG01952.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.155-1628A>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45008186 | |||||||
| chr19:45008269 | G | A | 1 | a0001c0001t0001g0138 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.155-1545G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45008269 | |||||||
| chr19:45008323 | C | A | 1 | a0001c0001t0002g0043 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.155-1491C>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45008323 | |||||||
| chr19:45008347 | C | T | 3 | a0001c0001t0001g0041 a0001c0001t0001g0128 a0001c0001t0001g0325 |
3 | HG02572.hp2 HG02622.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.155-1467C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45008347 | |||||||
| chr19:45008381 | G | A | 1 | a0001c0001t0001g0350 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.155-1433G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45008381 | |||||||
| chr19:45008403 | A | G | 2 | a0001c0001t0001g0193 a0001c0001t0002g0117 |
2 | NA18971.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.155-1411A>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45008403 | |||||||
| chr19:45008404 | C | A | 3 | a0001c0001t0001g0289 a0001c0001t0001g0343 a0001c0001t0001g0371 |
3 | HG02015.hp2 NA19080.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.155-1410C>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45008404 | |||||||
| chr19:45008874 | G | A | 1 | a0001c0001t0001g0029 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.155-940G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45008874 | |||||||
| chr19:45008970 | T | C | 21 | a0001c0001t0001g0009 a0001c0001t0001g0039 a0001c0001t0001g0042 others(18): Show |
21 | HG00733.hp2 HG01884.hp1 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.155-844T>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45008970 | |||||||
| chr19:45009106 | A | C | 7 | a0001c0001t0001g0130 a0001c0001t0001g0138 a0001c0001t0001g0374 others(4): Show |
7 | HG02109.hp1 HG02109.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.155-708A>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45009106 | |||||||
| chr19:45009157 | T | G | 17 | a0001c0001t0001g0002 a0001c0001t0001g0065 a0001c0001t0001g0073 others(14): Show |
18 | HG01069.hp2 HG01123.hp2 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.155-657T>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45009157 | |||||||
| chr19:45009167 | G | A | 5 | a0001c0001t0001g0303 a0001c0001t0001g0355 a0001c0001t0002g0280 others(2): Show |
5 | HG03491.hp1 HG03654.hp2 HG04228.hp2 others(2): Show |
intron_variant | MODIFIER | c.155-647G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45009167 | |||||||
| chr19:45009190 | C | T | 4 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 others(1): Show |
4 | HG02717.hp2 HG02976.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.155-624C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45009190 | |||||||
| chr19:45009205 | C | T | 2 | a0001c0001t0001g0141 a0001c0001t0001g0142 |
2 | HG02896.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.155-609C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45009205 | |||||||
| chr19:45009206 | G | A | 98 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0015 others(95): Show |
98 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(95): Show |
intron_variant | MODIFIER | c.155-608G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45009206 | |||||||
| chr19:45009301 | G | A | 1 | a0001c0001t0001g0212 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.155-513G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45009301 | |||||||
| chr19:45009418 | A | G | 19 | a0001c0001t0001g0009 a0001c0001t0001g0042 a0001c0001t0001g0087 others(16): Show |
19 | HG00733.hp2 HG01884.hp1 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.155-396A>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 2/11 | chr19 | 45009418 | |||||||
| chr19:45009888 | GGCCTTC | G | 74 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0027 others(71): Show |
74 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(71): Show |
intron_variant | MODIFIER | c.163+67_163+72delGC others(4): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | chr19 | 45009888 | |||||||
| chr19:45009956 | T | G | 1 | a0001c0001t0001g0123 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.163+134T>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | chr19 | 45009956 | |||||||
| chr19:45009978 | G | A | 70 | a0001c0001t0001g0002 a0001c0001t0001g0034 a0001c0001t0001g0035 others(67): Show |
71 | HG00673.hp1 HG00673.hp2 HG01109.hp1 others(68): Show |
intron_variant | MODIFIER | c.163+156G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | chr19 | 45009978 | |||||||
| chr19:45010159 | C | T | 59 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(56): Show |
59 | HG00673.hp1 HG00673.hp2 HG01109.hp1 others(56): Show |
intron_variant | MODIFIER | c.163+337C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | chr19 | 45010159 | |||||||
| chr19:45010200 | G | C | 19 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 others(16): Show |
19 | HG01891.hp2 HG02280.hp2 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.163+378G>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | chr19 | 45010200 | |||||||
| chr19:45010240 | T | G | 102 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0015 others(99): Show |
102 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(99): Show |
intron_variant | MODIFIER | c.163+418T>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | chr19 | 45010240 | |||||||
| chr19:45010293 | C | T | 97 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0015 others(94): Show |
97 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.163+471C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | chr19 | 45010293 | |||||||
| chr19:45010309 | T | C | 1 | a0001c0001t0001g0166 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.163+487T>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | chr19 | 45010309 | |||||||
| chr19:45010313 | T | TCAAAAAG others(315): Show |
1 | a0001c0001t0001g0009 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.163+507_163+508ins others(322): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45010313 | ||||||
| chr19:45010313 | T | TCAAAAAG others(314): Show |
6 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0235 others(3): Show |
6 | HG00733.hp2 HG01884.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.163+507_163+508ins others(321): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45010313 | ||||||
| chr19:45010313 | T | TCAAAAAG others(314): Show |
1 | a0001c0001t0001g0087 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.163+507_163+508ins others(321): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45010313 | ||||||
| chr19:45010313 | T | TCAAAAAG others(314): Show |
4 | a0001c0001t0001g0065 a0001c0001t0001g0073 a0001c0001t0001g0368 others(1): Show |
4 | HG01069.hp2 HG01123.hp2 HG01243.hp1 others(1): Show |
intron_variant | MODIFIER | c.163+507_163+508ins others(321): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45010313 | ||||||
| chr19:45010313 | T | TCAAAAAG others(313): Show |
1 | a0001c0001t0001g0138 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.163+507_163+508ins others(320): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45010313 | ||||||
| chr19:45010313 | T | TCAAAAAG others(312): Show |
6 | a0001c0001t0001g0130 a0001c0001t0001g0351 a0001c0002t0001g0104 others(3): Show |
6 | HG02109.hp2 HG02451.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.163+507_163+508ins others(319): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45010313 | ||||||
| chr19:45010313 | T | TCAAAAAG others(313): Show |
63 | a0001c0001t0001g0015 a0001c0001t0001g0027 a0001c0001t0001g0028 others(60): Show |
63 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.163+507_163+508ins others(320): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45010313 | ||||||
| chr19:45010313 | T | TCAAAAAG others(314): Show |
12 | a0001c0001t0001g0014 a0001c0001t0001g0113 a0001c0001t0001g0123 others(9): Show |
12 | HG00438.hp1 HG01175.hp2 HG01346.hp2 others(9): Show |
intron_variant | MODIFIER | c.163+507_163+508ins others(321): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45010313 | ||||||
| chr19:45010313 | T | TCAAAAAG others(315): Show |
1 | a0001c0001t0001g0107 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.163+507_163+508ins others(322): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45010313 | ||||||
| chr19:45010313 | T | TCAAAAAG others(313): Show |
1 | a0001c0001t0001g0374 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.163+507_163+508ins others(320): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45010313 | ||||||
| chr19:45010314 | C | CAAAAAGA others(313): Show |
2 | a0001c0001t0001g0167 a0001c0001t0001g0214 |
2 | HG01168.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.163+507_163+508ins others(320): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45010314 | ||||||
| chr19:45010314 | C | CAAAAAGA others(314): Show |
1 | a0001c0001t0001g0213 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.163+507_163+508ins others(321): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45010314 | ||||||
| chr19:45010350 | A | T | 1 | a0001c0001t0001g0026 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.163+528A>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | chr19 | 45010350 | |||||||
| chr19:45010357 | T | C | 99 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0015 others(96): Show |
99 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.163+535T>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | chr19 | 45010357 | |||||||
| chr19:45010451 | G | A | 1 | a0001c0001t0001g0029 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.163+629G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | chr19 | 45010451 | |||||||
| chr19:45010481 | A | G | 1 | a0001c0001t0001g0373 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.163+659A>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | chr19 | 45010481 | |||||||
| chr19:45010516 | T | G | 7 | a0001c0001t0001g0130 a0001c0001t0001g0138 a0001c0001t0001g0374 others(4): Show |
7 | HG02109.hp1 HG02109.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.163+694T>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | chr19 | 45010516 | |||||||
| chr19:45010596 | C | T | 2 | a0001c0001t0001g0064 a0001c0001t0001g0069 |
2 | HG01071.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.163+774C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | chr19 | 45010596 | |||||||
| chr19:45010720 | C | T | 1 | a0001c0001t0003g0189 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.163+898C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | chr19 | 45010720 | |||||||
| chr19:45010828 | C | A | 3 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0172 |
3 | HG02155.hp2 NA18998.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.163+1006C>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | chr19 | 45010828 | |||||||
| chr19:45010829 | C | A | 3 | a0001c0001t0001g0065 a0001c0001t0001g0073 a0001c0001t0001g0276 |
3 | HG01069.hp2 HG01123.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.163+1007C>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | chr19 | 45010829 | |||||||
| chr19:45010980 | C | T | 1 | a0001c0001t0001g0087 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.164-956C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | chr19 | 45010980 | |||||||
| chr19:45011174 | A | T | 2 | a0001c0001t0001g0138 a0001c0001t0001g0374 |
2 | HG02109.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.164-762A>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | chr19 | 45011174 | |||||||
| chr19:45011191 | C | G | 245 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0008 others(242): Show |
248 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(245): Show |
intron_variant | MODIFIER | c.164-745C>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | chr19 | 45011191 | |||||||
| chr19:45011204 | G | A | 1 | a0001c0001t0001g0231 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.164-732G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | chr19 | 45011204 | |||||||
| chr19:45011214 | G | A | 70 | a0001c0001t0001g0002 a0001c0001t0001g0034 a0001c0001t0001g0035 others(67): Show |
71 | HG00673.hp1 HG00673.hp2 HG01109.hp1 others(68): Show |
intron_variant | MODIFIER | c.164-722G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | chr19 | 45011214 | |||||||
| chr19:45011232 | G | A | 11 | a0001c0001t0001g0065 a0001c0001t0001g0073 a0001c0001t0001g0087 others(8): Show |
11 | HG01069.hp2 HG01123.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.164-704G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | chr19 | 45011232 | |||||||
| chr19:45011247 | C | T | 8 | a0001c0001t0001g0087 a0001c0001t0001g0130 a0001c0001t0001g0138 others(5): Show |
8 | HG02109.hp1 HG02109.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.164-689C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | chr19 | 45011247 | |||||||
| chr19:45011255 | C | T | 1 | a0001c0001t0001g0283 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.164-681C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | chr19 | 45011255 | |||||||
| chr19:45011272 | C | T | 2 | a0001c0001t0001g0193 a0001c0001t0002g0117 |
2 | NA18971.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.164-664C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | chr19 | 45011272 | |||||||
| chr19:45011292 | T | C | 263 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0008 others(260): Show |
266 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(263): Show |
intron_variant | MODIFIER | c.164-644T>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | chr19 | 45011292 | |||||||
| chr19:45011408 | C | T | 1 | a0001c0001t0001g0026 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.164-528C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | chr19 | 45011408 | |||||||
| chr19:45011418 | T | C | 1 | a0001c0001t0001g0299 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.164-518T>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | chr19 | 45011418 | |||||||
| chr19:45011419 | C | T | 1 | a0001c0001t0001g0299 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.164-517C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | chr19 | 45011419 | |||||||
| chr19:45011443 | T | G | 79 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0027 others(76): Show |
79 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.164-493T>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | chr19 | 45011443 | |||||||
| chr19:45011455 | C | T | 2 | a0001c0001t0001g0039 a0001c0001t0001g0367 |
2 | HG02965.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.164-481C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | chr19 | 45011455 | |||||||
| chr19:45011488 | A | G | 5 | a0001c0001t0001g0130 a0001c0002t0001g0104 a0001c0002t0001g0131 others(2): Show |
5 | HG02109.hp2 HG02451.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.164-448A>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | chr19 | 45011488 | |||||||
| chr19:45011519 | C | T | 1 | a0001c0001t0001g0301 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.164-417C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | chr19 | 45011519 | |||||||
| chr19:45011756 | C | CTG | 10 | a0001c0001t0001g0076 a0001c0001t0001g0112 a0001c0001t0001g0124 others(7): Show |
10 | HG01255.hp1 HG01884.hp2 HG02155.hp1 others(7): Show |
intron_variant | MODIFIER | c.164-139_164-138dup others(2): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011756 | ||||||
| chr19:45011756 | C | CTGTG | 6 | a0001c0001t0001g0050 a0001c0001t0001g0087 a0001c0001t0001g0103 others(3): Show |
6 | HG01943.hp2 HG02647.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.164-141_164-138dup others(4): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011756 | ||||||
| chr19:45011756 | C | CTGTGTG | 6 | a0001c0001t0001g0044 a0001c0001t0001g0128 a0001c0001t0001g0208 others(3): Show |
6 | HG00140.hp2 HG01192.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.164-143_164-138dup others(6): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011756 | ||||||
| chr19:45011756 | C | CTGTGTGT others(3): Show |
1 | a0001c0001t0001g0041 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.164-147_164-138dup others(10): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011756 | ||||||
| chr19:45011756 | C | CTGTGTGT others(5): Show |
2 | a0001c0001t0001g0060 a0001c0001t0002g0091 |
2 | HG02004.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.164-149_164-138dup others(12): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011756 | ||||||
| chr19:45011756 | C | CTGTGTGT others(7): Show |
2 | a0001c0001t0001g0047 a0001c0001t0001g0061 |
2 | HG00323.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.164-151_164-138dup others(14): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011756 | ||||||
| chr19:45011756 | C | CTGTGTGT others(9): Show |
3 | a0001c0001t0001g0048 a0001c0001t0001g0062 a0001c0001t0001g0072 |
3 | HG01934.hp1 HG01952.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.164-153_164-138dup others(16): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011756 | ||||||
| chr19:45011756 | C | CTGTGTGT others(13): Show |
2 | a0001c0001t0001g0063 a0001c0001t0001g0086 |
2 | HG01496.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.164-157_164-138dup others(20): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011756 | ||||||
| chr19:45011756 | C | G | 5 | a0001c0001t0001g0130 a0001c0002t0001g0104 a0001c0002t0001g0131 others(2): Show |
5 | HG02109.hp2 HG02451.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.164-180C>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | chr19 | 45011756 | |||||||
| chr19:45011789 | T | A | 1 | a0001c0004t0001g0241 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.164-147T>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | chr19 | 45011789 | |||||||
| chr19:45011791 | T | A | 2 | a0001c0001t0001g0374 a0001c0004t0001g0241 |
2 | HG02109.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.164-145T>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | chr19 | 45011791 | |||||||
| chr19:45011793 | T | A | 2 | a0001c0001t0001g0374 a0001c0004t0001g0241 |
2 | HG02109.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.164-143T>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | chr19 | 45011793 | |||||||
| chr19:45011793 | TGTGTGAG others(11): Show |
T | 1 | a0001c0001t0001g0355 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.164-141_164-124del others(18): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011793 | ||||||
| chr19:45011795 | T | A | 3 | a0001c0001t0001g0138 a0001c0001t0001g0374 a0001c0004t0001g0241 |
3 | HG02109.hp1 HG03041.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.164-141T>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | chr19 | 45011795 | |||||||
| chr19:45011795 | TGTGAGAG others(5): Show |
T | 1 | a0001c0001t0001g0026 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.164-139_164-128del others(12): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011795 | ||||||
| chr19:45011795 | TGTGAGAG others(9): Show |
T | 3 | a0001c0001t0001g0352 a0001c0001t0001g0353 a0001c0001t0001g0354 |
3 | HG01123.hp1 HG02055.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.164-139_164-124del others(16): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011795 | ||||||
| chr19:45011795 | TGTGAGAG others(11): Show |
T | 4 | a0001c0001t0001g0079 a0001c0001t0001g0082 a0001c0001t0001g0084 others(1): Show |
4 | HG01109.hp2 HG02683.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.164-139_164-122del others(18): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011795 | ||||||
| chr19:45011795 | TGTGAGAG others(13): Show |
T | 1 | a0001c0001t0001g0042 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.164-139_164-120del others(20): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011795 | ||||||
| chr19:45011797 | T | A | 4 | a0001c0001t0001g0138 a0001c0001t0001g0374 a0001c0002t0001g0131 others(1): Show |
4 | HG02109.hp1 HG02109.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.164-139T>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | chr19 | 45011797 | |||||||
| chr19:45011797 | T | TGAGAGAG others(13): Show |
1 | a0001c0001t0001g0286 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.164-120_164-101dup others(20): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011797 | ||||||
| chr19:45011797 | T | TGTGAGAG others(3): Show |
2 | a0001c0001t0001g0065 a0001c0001t0001g0073 |
2 | HG01069.hp2 HG01123.hp2 |
intron_variant | MODIFIER | c.164-138_164-137ins others(10): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011797 | ||||||
| chr19:45011797 | T | TGTGAGAG others(5): Show |
1 | a0001c0001t0003g0010 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.164-138_164-137ins others(12): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011797 | ||||||
| chr19:45011797 | T | TGTGAGAG others(7): Show |
1 | a0001c0001t0001g0250 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.164-138_164-137ins others(14): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011797 | ||||||
| chr19:45011797 | T | TGTGAGAG others(9): Show |
1 | a0001c0001t0001g0017 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.164-138_164-137ins others(16): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011797 | ||||||
| chr19:45011797 | T | TGTGAGAG others(11): Show |
1 | a0001c0001t0001g0016 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.164-138_164-137ins others(18): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011797 | ||||||
| chr19:45011797 | T | TGTGAGAG others(13): Show |
1 | a0001c0001t0001g0234 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.164-138_164-137ins others(20): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011797 | ||||||
| chr19:45011797 | T | TGTGTGAG others(7): Show |
4 | a0001c0001t0001g0083 a0001c0001t0001g0126 a0001c0001t0001g0127 others(1): Show |
4 | HG00438.hp2 HG01106.hp2 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.164-138_164-137ins others(14): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011797 | ||||||
| chr19:45011797 | T | TGTGTGAG others(9): Show |
5 | a0001c0001t0001g0013 a0001c0001t0001g0129 a0001c0001t0001g0232 others(2): Show |
5 | HG02015.hp2 HG02738.hp1 NA18939.hp1 others(2): Show |
intron_variant | MODIFIER | c.164-138_164-137ins others(16): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011797 | ||||||
| chr19:45011797 | T | TGTGTGAG others(11): Show |
2 | a0001c0001t0001g0152 a0001c0001t0001g0247 |
2 | HG02071.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.164-138_164-137ins others(18): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011797 | ||||||
| chr19:45011797 | T | TGTGTGAG others(13): Show |
2 | a0001c0001t0001g0012 a0001c0001t0001g0243 |
2 | HG03704.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.164-138_164-137ins others(20): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011797 | ||||||
| chr19:45011797 | T | TGTGTGAG others(17): Show |
2 | a0001c0001t0001g0089 a0001c0001t0001g0121 |
2 | NA19082.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.164-138_164-137ins others(24): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011797 | ||||||
| chr19:45011797 | T | TGTGTGTG others(3): Show |
1 | a0001c0001t0001g0045 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.164-138_164-137ins others(10): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011797 | ||||||
| chr19:45011797 | T | TGTGTGTG others(5): Show |
2 | a0001c0001t0001g0004 a0001c0001t0001g0049 |
2 | HG02922.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.164-138_164-137ins others(12): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011797 | ||||||
| chr19:45011797 | T | TGTGTGTG others(7): Show |
2 | a0001c0001t0001g0106 a0001c0001t0001g0155 |
2 | HG00544.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.164-138_164-137ins others(14): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011797 | ||||||
| chr19:45011797 | T | TGTGTGTG others(11): Show |
6 | a0001c0001t0001g0085 a0001c0001t0001g0105 a0001c0001t0001g0283 others(3): Show |
6 | HG01255.hp2 HG02040.hp1 HG02293.hp1 others(3): Show |
intron_variant | MODIFIER | c.164-138_164-137ins others(18): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011797 | ||||||
| chr19:45011797 | T | TGTGTGTG others(13): Show |
4 | a0001c0001t0001g0031 a0001c0001t0001g0080 a0001c0001t0001g0248 others(1): Show |
4 | HG00597.hp2 HG00609.hp2 HG02523.hp2 others(1): Show |
intron_variant | MODIFIER | c.164-138_164-137ins others(20): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011797 | ||||||
| chr19:45011797 | T | TGTGTGTG others(15): Show |
2 | a0001c0001t0001g0018 a0001c0001t0001g0019 |
2 | HG01981.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.164-138_164-137ins others(22): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011797 | ||||||
| chr19:45011797 | T | TGTGTGTG others(21): Show |
1 | a0001c0001t0001g0006 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.164-138_164-137ins others(28): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011797 | ||||||
| chr19:45011797 | T | TGTGTGTG others(5): Show |
3 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0071 |
4 | HG01168.hp1 HG03490.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.164-138_164-137ins others(12): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011797 | ||||||
| chr19:45011797 | T | TGTGTGTG others(7): Show |
3 | a0001c0001t0001g0004 a0001c0001t0001g0058 a0001c0001t0001g0366 |
3 | HG00621.hp2 HG02965.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.164-138_164-137ins others(14): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011797 | ||||||
| chr19:45011797 | T | TGTGTGTG others(9): Show |
1 | a0001c0001t0001g0154 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.164-138_164-137ins others(16): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011797 | ||||||
| chr19:45011797 | T | TGTGTGTG others(11): Show |
2 | a0001c0001t0001g0059 a0001c0001t0001g0102 |
2 | NA18953.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.164-138_164-137ins others(18): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011797 | ||||||
| chr19:45011797 | T | TGTGTGTG others(13): Show |
3 | a0001c0001t0001g0057 a0001c0001t0001g0288 a0001c0001t0001g0298 |
3 | HG02056.hp1 NA18997.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.164-138_164-137ins others(20): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011797 | ||||||
| chr19:45011797 | T | TGTGTGTG others(15): Show |
5 | a0001c0001t0001g0022 a0001c0001t0001g0051 a0001c0001t0001g0237 others(2): Show |
5 | HG00423.hp1 HG01943.hp1 NA18988.hp2 others(2): Show |
intron_variant | MODIFIER | c.164-138_164-137ins others(22): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011797 | ||||||
| chr19:45011797 | T | TGTGTGTG others(17): Show |
3 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0203 |
3 | HG02293.hp2 HG03209.hp1 NA18952.hp2 |
intron_variant | MODIFIER | c.164-138_164-137ins others(24): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011797 | ||||||
| chr19:45011797 | T | TGTGTGTG others(19): Show |
2 | a0001c0001t0001g0006 a0001c0001t0001g0024 |
2 | HG01074.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.164-138_164-137ins others(26): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011797 | ||||||
| chr19:45011797 | T | TGTGTGTG others(21): Show |
1 | a0001c0001t0001g0025 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.164-138_164-137ins others(28): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011797 | ||||||
| chr19:45011797 | T | TGTGTGTG others(23): Show |
1 | a0001c0001t0001g0246 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.164-138_164-137ins others(30): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011797 | ||||||
| chr19:45011797 | T | TGTGTGTG others(25): Show |
1 | a0001c0001t0001g0276 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.164-138_164-137ins others(32): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011797 | ||||||
| chr19:45011797 | T | TGTGTGTG others(14): Show |
1 | a0001c0001t0001g0067 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.164-138_164-137ins others(21): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011797 | ||||||
| chr19:45011797 | T | TGTGTGTG others(9): Show |
2 | a0001c0001t0001g0074 a0001c0001t0001g0153 |
2 | HG03486.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.164-138_164-137ins others(16): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011797 | ||||||
| chr19:45011797 | T | TGTGTGTG others(11): Show |
4 | a0001c0001t0001g0003 a0001c0001t0001g0093 a0001c0001t0001g0094 others(1): Show |
4 | HG00099.hp2 HG01256.hp1 NA18977.hp1 others(1): Show |
intron_variant | MODIFIER | c.164-138_164-137ins others(18): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011797 | ||||||
| chr19:45011797 | T | TGTGTGTG others(13): Show |
2 | a0001c0001t0001g0081 a0001c0001t0001g0321 |
2 | HG00609.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.164-138_164-137ins others(20): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011797 | ||||||
| chr19:45011797 | T | TGTGTGTG others(15): Show |
4 | a0001c0001t0001g0146 a0001c0001t0001g0296 a0001c0001t0002g0068 others(1): Show |
4 | HG00423.hp2 HG01071.hp2 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.164-138_164-137ins others(22): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011797 | ||||||
| chr19:45011797 | T | TGTGTGTG others(17): Show |
2 | a0001c0001t0001g0289 a0001c0001t0001g0320 |
2 | HG01358.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.164-138_164-137ins others(24): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011797 | ||||||
| chr19:45011797 | T | TGTGTGTG others(21): Show |
2 | a0001c0001t0001g0007 a0001c0001t0001g0020 |
2 | NA18975.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.164-138_164-137ins others(28): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011797 | ||||||
| chr19:45011797 | T | TGTGTGTG others(23): Show |
1 | a0001c0001t0001g0242 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.164-138_164-137ins others(30): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011797 | ||||||
| chr19:45011797 | T | TGTGTGTG others(9): Show |
1 | a0001c0001t0001g0372 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.164-138_164-137ins others(16): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011797 | ||||||
| chr19:45011797 | T | TGTGTGTG others(11): Show |
2 | a0001c0001t0001g0365 a0001c0001t0003g0245 |
2 | HG01361.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.164-138_164-137ins others(18): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011797 | ||||||
| chr19:45011797 | T | TGTGTGTG others(13): Show |
5 | a0001c0001t0001g0003 a0001c0001t0001g0052 a0001c0001t0001g0090 others(2): Show |
5 | HG01257.hp1 HG01515.hp2 HG01517.hp1 others(2): Show |
intron_variant | MODIFIER | c.164-138_164-137ins others(20): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011797 | ||||||
| chr19:45011797 | T | TGTGTGTG others(15): Show |
1 | a0001c0001t0001g0343 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.164-138_164-137ins others(22): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011797 | ||||||
| chr19:45011797 | T | TGTGTGTG others(19): Show |
1 | a0001c0001t0001g0249 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.164-138_164-137ins others(26): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011797 | ||||||
| chr19:45011797 | T | TGTGTGTG others(9): Show |
1 | a0001c0001t0001g0240 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.164-138_164-137ins others(16): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011797 | ||||||
| chr19:45011797 | T | TGTGTGTG others(13): Show |
2 | a0001c0001t0001g0046 a0001c0001t0001g0070 |
2 | HG03130.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.164-138_164-137ins others(20): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011797 | ||||||
| chr19:45011797 | T | TGTGTGTG others(21): Show |
1 | a0001c0001t0002g0043 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.164-138_164-137ins others(28): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011797 | ||||||
| chr19:45011797 | T | TGTGTGTG others(11): Show |
1 | a0001c0001t0001g0054 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.164-138_164-137ins others(18): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011797 | ||||||
| chr19:45011797 | T | TGTGTGTG others(13): Show |
1 | a0001c0001t0001g0075 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.164-138_164-137ins others(20): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011797 | ||||||
| chr19:45011797 | T | TGTGTGTG others(17): Show |
1 | a0001c0001t0001g0150 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.164-138_164-137ins others(24): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011797 | ||||||
| chr19:45011797 | T | TGTGTGTG others(19): Show |
1 | a0001c0001t0001g0066 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.164-138_164-137ins others(26): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011797 | ||||||
| chr19:45011797 | T | TGTGTGTG others(17): Show |
1 | a0001c0001t0001g0297 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.164-138_164-137ins others(24): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011797 | ||||||
| chr19:45011797 | TGA | T | 21 | a0001c0001t0001g0096 a0001c0001t0001g0100 a0001c0001t0001g0149 others(18): Show |
21 | HG01175.hp1 HG01517.hp2 HG01928.hp1 others(18): Show |
intron_variant | MODIFIER | c.164-102_164-101del others(2): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011797 | ||||||
| chr19:45011797 | TGAGA | T | 34 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(31): Show |
34 | HG00673.hp2 HG00733.hp1 HG01099.hp2 others(31): Show |
intron_variant | MODIFIER | c.164-104_164-101del others(4): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011797 | ||||||
| chr19:45011797 | TGAGAGA | T | 42 | a0001c0001t0001g0005 a0001c0001t0001g0029 a0001c0001t0001g0030 others(39): Show |
42 | HG00140.hp1 HG00408.hp1 HG00558.hp2 others(39): Show |
intron_variant | MODIFIER | c.164-106_164-101del others(6): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011797 | ||||||
| chr19:45011797 | TGAGAGAG others(1): Show |
T | 33 | a0001c0001t0001g0008 a0001c0001t0001g0014 a0001c0001t0001g0015 others(30): Show |
34 | HG00099.hp1 HG00639.hp1 HG00735.hp1 others(31): Show |
intron_variant | MODIFIER | c.164-108_164-101del others(8): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011797 | ||||||
| chr19:45011797 | TGAGAGAG others(3): Show |
T | 37 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0032 others(34): Show |
37 | HG00438.hp1 HG00639.hp2 HG00733.hp2 others(34): Show |
intron_variant | MODIFIER | c.164-110_164-101del others(10): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011797 | ||||||
| chr19:45011797 | TGAGAGAG others(5): Show |
T | 18 | a0001c0001t0001g0002 a0001c0001t0001g0034 a0001c0001t0001g0077 others(15): Show |
18 | HG00558.hp1 HG00597.hp1 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.164-112_164-101del others(12): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011797 | ||||||
| chr19:45011797 | TGAGAGAG others(7): Show |
T | 11 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0165 others(8): Show |
11 | HG00544.hp1 HG01243.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.164-114_164-101del others(14): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011797 | ||||||
| chr19:45011797 | TGAGAGAG others(9): Show |
T | 4 | a0001c0001t0001g0040 a0001c0001t0001g0101 a0001c0001t0001g0123 others(1): Show |
4 | HG01891.hp1 HG03209.hp2 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.164-116_164-101del others(16): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011797 | ||||||
| chr19:45011797 | TGAGAGAG others(13): Show |
T | 1 | a0001c0001t0001g0039 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.164-120_164-101del others(20): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011797 | ||||||
| chr19:45011799 | A | T | 45 | a0001c0001t0001g0038 a0001c0001t0001g0041 a0001c0001t0001g0044 others(42): Show |
45 | HG00140.hp2 HG00673.hp1 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.164-137A>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | chr19 | 45011799 | |||||||
| chr19:45011801 | A | T | 65 | a0001c0001t0001g0038 a0001c0001t0001g0041 a0001c0001t0001g0044 others(62): Show |
65 | HG00140.hp2 HG00673.hp1 HG00738.hp2 others(62): Show |
intron_variant | MODIFIER | c.164-135A>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | chr19 | 45011801 | |||||||
| chr19:45011803 | A | T | 97 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(94): Show |
97 | HG00673.hp1 HG00673.hp2 HG00733.hp1 others(94): Show |
intron_variant | MODIFIER | c.164-133A>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | chr19 | 45011803 | |||||||
| chr19:45011805 | A | T | 134 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0027 others(131): Show |
134 | HG00140.hp1 HG00408.hp1 HG00558.hp2 others(131): Show |
intron_variant | MODIFIER | c.164-131A>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | chr19 | 45011805 | |||||||
| chr19:45011807 | A | T | 165 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(162): Show |
166 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.164-129A>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | chr19 | 45011807 | |||||||
| chr19:45011809 | A | T | 196 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0008 others(193): Show |
198 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(195): Show |
intron_variant | MODIFIER | c.164-127A>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | chr19 | 45011809 | |||||||
| chr19:45011811 | A | T | 182 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0008 others(179): Show |
184 | HG00099.hp1 HG00140.hp1 HG00438.hp1 others(181): Show |
intron_variant | MODIFIER | c.164-125A>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | chr19 | 45011811 | |||||||
| chr19:45011813 | A | T | 95 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0014 others(92): Show |
96 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.164-123A>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | chr19 | 45011813 | |||||||
| chr19:45011815 | A | T | 74 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0014 others(71): Show |
75 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.164-121A>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | chr19 | 45011815 | |||||||
| chr19:45011817 | A | T | 13 | a0001c0001t0001g0002 a0001c0001t0001g0077 a0001c0001t0001g0092 others(10): Show |
14 | HG00544.hp1 HG01891.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.164-119A>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | chr19 | 45011817 | |||||||
| chr19:45011819 | A | T | 3 | a0001c0001t0001g0039 a0001c0001t0001g0362 a0001c0001t0001g0367 |
3 | HG02258.hp1 HG02965.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.164-117A>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | chr19 | 45011819 | |||||||
| chr19:45011821 | A | T | 2 | a0001c0001t0001g0039 a0001c0001t0001g0367 |
2 | HG02965.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.164-115A>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | chr19 | 45011821 | |||||||
| chr19:45011872 | C | CT | 6 | a0001c0001t0001g0067 a0001c0001t0001g0303 a0001c0001t0002g0068 others(3): Show |
6 | HG02602.hp1 HG02602.hp2 HG03491.hp1 others(3): Show |
intron_variant | MODIFIER | c.164-49dupT | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011872 | ||||||
| chr19:45011872 | CT | C | 38 | a0001c0001t0001g0002 a0001c0001t0001g0031 a0001c0001t0001g0041 others(35): Show |
39 | HG00099.hp1 HG00597.hp2 HG01071.hp1 others(36): Show |
intron_variant | MODIFIER | c.164-49delT | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 45011872 | ||||||
| chr19:45011890 | T | G | 1 | a0001c0001t0001g0373 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.164-46T>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 3/11 | chr19 | 45011890 | |||||||
| chr19:45012297 | C | T | 1 | a0001c0001t0001g0326 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.504+21C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45012297 | |||||||
| chr19:45012315 | G | A | 7 | a0001c0001t0001g0130 a0001c0001t0001g0138 a0001c0001t0001g0374 others(4): Show |
7 | HG02109.hp1 HG02109.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.504+39G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45012315 | |||||||
| chr19:45012518 | C | T | 2 | a0001c0001t0001g0079 a0001c0001t0001g0082 |
2 | HG01109.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.504+242C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45012518 | |||||||
| chr19:45012595 | T | C | 2 | a0001c0001t0001g0065 a0001c0001t0001g0073 |
2 | HG01069.hp2 HG01123.hp2 |
intron_variant | MODIFIER | c.504+319T>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45012595 | |||||||
| chr19:45012667 | G | T | 1 | a0001c0001t0001g0373 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.504+391G>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45012667 | |||||||
| chr19:45012744 | A | G | 3 | a0001c0001t0001g0167 a0001c0001t0001g0213 a0001c0001t0001g0214 |
3 | HG00639.hp2 HG01168.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.504+468A>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45012744 | |||||||
| chr19:45012745 | A | G | 1 | a0001c0001t0001g0224 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.504+469A>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45012745 | |||||||
| chr19:45012746 | G | A | 1 | a0001c0001t0001g0224 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.504+470G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45012746 | |||||||
| chr19:45012746 | G | GA | 163 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0014 others(160): Show |
165 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.504+482dupA | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr19 | 45012746 | ||||||
| chr19:45012792 | T | C | 173 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(170): Show |
175 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(172): Show |
intron_variant | MODIFIER | c.504+516T>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45012792 | |||||||
| chr19:45012814 | C | T | 1 | a0001c0001t0001g0276 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.504+538C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45012814 | |||||||
| chr19:45012879 | T | G | 7 | a0001c0001t0001g0130 a0001c0001t0001g0138 a0001c0001t0001g0374 others(4): Show |
7 | HG02109.hp1 HG02109.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.504+603T>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45012879 | |||||||
| chr19:45013128 | A | G | 2 | a0001c0001t0001g0187 a0001c0001t0001g0304 |
2 | HG00558.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.504+852A>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45013128 | |||||||
| chr19:45013197 | A | G | 3 | a0001c0001t0001g0212 a0001c0001t0001g0342 a0001c0001t0001g0351 |
3 | HG01109.hp1 HG02735.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.504+921A>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45013197 | |||||||
| chr19:45013211 | G | A | 78 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0027 others(75): Show |
78 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.504+935G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45013211 | |||||||
| chr19:45013234 | C | T | 2 | a0001c0001t0001g0078 a0001c0001t0001g0097 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.504+958C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45013234 | |||||||
| chr19:45013303 | CTAATTTT others(12): Show |
C | 1 | a0001c0001t0001g0299 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.504+1030_504+1048d others(21): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr19 | 45013303 | ||||||
| chr19:45013341 | A | G | 2 | a0001c0001t0001g0039 a0001c0001t0001g0367 |
2 | HG02965.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.504+1065A>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45013341 | |||||||
| chr19:45013373 | T | A | 75 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0029 others(72): Show |
77 | HG00140.hp1 HG00408.hp1 HG00621.hp1 others(74): Show |
intron_variant | MODIFIER | c.504+1097T>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45013373 | |||||||
| chr19:45013437 | G | C | 3 | a0001c0001t0001g0041 a0001c0001t0001g0128 a0001c0001t0001g0325 |
3 | HG02572.hp2 HG02622.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.504+1161G>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45013437 | |||||||
| chr19:45013445 | T | C | 7 | a0001c0001t0001g0130 a0001c0001t0001g0138 a0001c0001t0001g0374 others(4): Show |
7 | HG02109.hp1 HG02109.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.504+1169T>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45013445 | |||||||
| chr19:45013455 | T | TAC | 96 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0013 others(93): Show |
98 | HG00408.hp2 HG00423.hp1 HG00609.hp2 others(95): Show |
intron_variant | MODIFIER | c.504+1180_504+1181i others(4): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr19 | 45013455 | ||||||
| chr19:45013491 | C | T | 8 | a0001c0001t0001g0130 a0001c0001t0001g0138 a0001c0001t0001g0373 others(5): Show |
8 | HG02109.hp1 HG02109.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.504+1215C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45013491 | |||||||
| chr19:45013520 | C | T | 1 | a0001c0001t0001g0087 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.504+1244C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45013520 | |||||||
| chr19:45013623 | G | A | 69 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0035 others(66): Show |
70 | HG00408.hp2 HG00423.hp1 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.504+1347G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45013623 | |||||||
| chr19:45013959 | T | C | 4 | a0001c0001t0001g0190 a0001c0001t0001g0191 a0001c0001t0001g0192 others(1): Show |
4 | HG02647.hp1 HG02886.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.504+1683T>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45013959 | |||||||
| chr19:45014010 | T | C | 1 | a0001c0001t0001g0166 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.504+1734T>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45014010 | |||||||
| chr19:45014027 | C | T | 1 | a0001c0001t0001g0326 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.504+1751C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45014027 | |||||||
| chr19:45014115 | T | C | 1 | a0001c0001t0001g0026 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.504+1839T>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45014115 | |||||||
| chr19:45014128 | C | T | 1 | a0001c0001t0001g0035 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.504+1852C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45014128 | |||||||
| chr19:45014168 | C | CT | 85 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0009 others(82): Show |
87 | HG00408.hp2 HG00423.hp1 HG00609.hp2 others(84): Show |
intron_variant | MODIFIER | c.504+1910dupT | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr19 | 45014168 | ||||||
| chr19:45014168 | C | CTT | 9 | a0001c0001t0001g0013 a0001c0001t0001g0077 a0001c0001t0001g0121 others(6): Show |
9 | HG02145.hp1 HG02257.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.504+1909_504+1910d others(4): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr19 | 45014168 | ||||||
| chr19:45014168 | CTTTT | C | 41 | a0001c0001t0001g0007 a0001c0001t0001g0016 a0001c0001t0001g0017 others(38): Show |
42 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(39): Show |
intron_variant | MODIFIER | c.504+1907_504+1910d others(6): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr19 | 45014168 | ||||||
| chr19:45014238 | C | T | 1 | a0001c0001t0001g0066 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.504+1962C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45014238 | |||||||
| chr19:45014239 | G | A | 68 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0035 others(65): Show |
69 | HG00408.hp2 HG00423.hp1 HG00609.hp2 others(66): Show |
intron_variant | MODIFIER | c.504+1963G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45014239 | |||||||
| chr19:45014255 | C | T | 1 | a0001c0001t0001g0311 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.504+1979C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45014255 | |||||||
| chr19:45014263 | A | T | 1 | a0001c0001t0001g0094 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.504+1987A>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45014263 | |||||||
| chr19:45014527 | G | GT | 260 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(257): Show |
264 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(261): Show |
intron_variant | MODIFIER | c.504+2261dupT | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr19 | 45014527 | ||||||
| chr19:45014528 | T | G | 1 | a0001c0001t0001g0087 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.504+2252T>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45014528 | |||||||
| chr19:45014666 | C | T | 3 | a0001c0001t0001g0065 a0001c0001t0001g0073 a0001c0001t0001g0276 |
3 | HG01069.hp2 HG01123.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.504+2390C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45014666 | |||||||
| chr19:45014815 | G | A | 2 | a0001c0001t0001g0003 a0001c0001t0001g0090 |
3 | HG01256.hp1 HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.504+2539G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45014815 | |||||||
| chr19:45014852 | T | C | 1 | a0001c0001t0001g0373 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.504+2576T>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45014852 | |||||||
| chr19:45014903 | AT | A | 258 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(255): Show |
262 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(259): Show |
intron_variant | MODIFIER | c.504+2644delT | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr19 | 45014903 | ||||||
| chr19:45014965 | T | C | 280 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(277): Show |
284 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(281): Show |
intron_variant | MODIFIER | c.504+2689T>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45014965 | |||||||
| chr19:45014988 | C | T | 6 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0235 others(3): Show |
6 | HG00733.hp2 HG01884.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.504+2712C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45014988 | |||||||
| chr19:45014989 | G | A | 1 | a0001c0001t0001g0123 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.504+2713G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45014989 | |||||||
| chr19:45015087 | G | A | 1 | a0001c0001t0001g0153 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.504+2811G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45015087 | |||||||
| chr19:45015164 | A | G | 1 | a0001c0001t0002g0363 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.504+2888A>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45015164 | |||||||
| chr19:45015281 | C | T | 1 | a0001c0001t0001g0373 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.504+3005C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45015281 | |||||||
| chr19:45015411 | C | A | 1 | a0001c0001t0001g0123 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.504+3135C>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45015411 | |||||||
| chr19:45015459 | G | T | 3 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0225 |
3 | HG02647.hp1 HG02970.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.504+3183G>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45015459 | |||||||
| chr19:45015579 | A | T | 3 | a0001c0001t0001g0084 a0001c0001t0001g0269 a0001c0001t0001g0310 |
3 | HG02683.hp2 HG03239.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.504+3303A>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45015579 | |||||||
| chr19:45015595 | C | T | 1 | a0001c0001t0001g0138 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.504+3319C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45015595 | |||||||
| chr19:45015730 | A | G | 326 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(323): Show |
331 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(328): Show |
intron_variant | MODIFIER | c.504+3454A>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45015730 | |||||||
| chr19:45015734 | C | CA | 8 | a0001c0001t0001g0041 a0001c0001t0001g0065 a0001c0001t0001g0073 others(5): Show |
8 | HG01069.hp2 HG01123.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.504+3470dupA | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr19 | 45015734 | ||||||
| chr19:45015734 | C | CAA | 7 | a0001c0001t0001g0130 a0001c0001t0001g0138 a0001c0001t0001g0374 others(4): Show |
7 | HG02109.hp1 HG02109.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.504+3469_504+3470d others(4): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr19 | 45015734 | ||||||
| chr19:45015744 | AAAG | A | 6 | a0001c0001t0001g0097 a0001c0001t0001g0254 a0001c0001t0001g0264 others(3): Show |
6 | HG02897.hp2 NA18747.hp2 NA18946.hp1 others(3): Show |
intron_variant | MODIFIER | c.504+3471_504+3473d others(5): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr19 | 45015744 | ||||||
| chr19:45015745 | AAG | A | 79 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0029 others(76): Show |
81 | HG00140.hp1 HG00408.hp1 HG00621.hp1 others(78): Show |
intron_variant | MODIFIER | c.504+3471_504+3472d others(4): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr19 | 45015745 | ||||||
| chr19:45015746 | AG | A | 161 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0009 others(158): Show |
163 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(160): Show |
intron_variant | MODIFIER | c.504+3471delG | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45015746 | |||||||
| chr19:45015747 | G | A | 29 | a0001c0001t0001g0013 a0001c0001t0001g0034 a0001c0001t0001g0041 others(26): Show |
29 | HG01069.hp2 HG01109.hp2 HG01123.hp2 others(26): Show |
intron_variant | MODIFIER | c.504+3471G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45015747 | |||||||
| chr19:45015842 | G | A | 262 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(259): Show |
266 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(263): Show |
intron_variant | MODIFIER | c.504+3566G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45015842 | |||||||
| chr19:45015954 | A | G | 1 | a0001c0001t0001g0164 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.504+3678A>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45015954 | |||||||
| chr19:45016006 | A | AT | 9 | a0001c0001t0001g0013 a0001c0001t0001g0034 a0001c0001t0001g0040 others(6): Show |
9 | HG01109.hp2 HG02055.hp1 HG02683.hp2 others(6): Show |
intron_variant | MODIFIER | c.504+3740dupT | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr19 | 45016006 | ||||||
| chr19:45016006 | A | T | 77 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0027 others(74): Show |
77 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.504+3730A>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45016006 | |||||||
| chr19:45016009 | T | A | 1 | a0001c0001t0001g0026 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.504+3733T>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45016009 | |||||||
| chr19:45016048 | G | C | 2 | a0001c0001t0001g0331 a0001c0001t0001g0340 |
2 | NA18961.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.504+3772G>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45016048 | |||||||
| chr19:45016099 | C | G | 1 | a0001c0001t0001g0282 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.504+3823C>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45016099 | |||||||
| chr19:45016233 | C | T | 1 | a0001c0002t0001g0104 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.504+3957C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45016233 | |||||||
| chr19:45016240 | C | A | 1 | a0001c0001t0001g0247 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.504+3964C>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45016240 | |||||||
| chr19:45016321 | GAGAA | G | 6 | a0001c0001t0001g0041 a0001c0001t0001g0065 a0001c0001t0001g0073 others(3): Show |
6 | HG01069.hp2 HG01123.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.504+4051_504+4054d others(6): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr19 | 45016321 | ||||||
| chr19:45016541 | C | T | 1 | a0001c0001t0001g0190 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.504+4265C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45016541 | |||||||
| chr19:45016776 | G | C | 7 | a0001c0001t0001g0009 a0001c0001t0001g0160 a0001c0001t0001g0161 others(4): Show |
7 | HG00733.hp2 HG01884.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.504+4500G>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45016776 | |||||||
| chr19:45016850 | A | AAAAC | 16 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0165 others(13): Show |
16 | HG00544.hp1 HG02129.hp1 NA18941.hp2 others(13): Show |
intron_variant | MODIFIER | c.504+4598_504+4601d others(6): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr19 | 45016850 | ||||||
| chr19:45016850 | AAAACAAA others(1): Show |
A | 3 | a0001c0001t0001g0041 a0001c0001t0001g0128 a0001c0001t0001g0325 |
3 | HG02572.hp2 HG02622.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.504+4594_504+4601d others(10): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr19 | 45016850 | ||||||
| chr19:45017027 | A | C | 13 | a0001c0001t0001g0002 a0001c0001t0001g0077 a0001c0001t0001g0092 others(10): Show |
14 | HG01891.hp1 HG02145.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.504+4751A>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45017027 | |||||||
| chr19:45017246 | T | G | 2 | a0001c0001t0001g0179 a0001c0001t0001g0180 |
2 | NA19056.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.505-4807T>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45017246 | |||||||
| chr19:45017254 | G | A | 1 | a0001c0001t0001g0009 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.505-4799G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45017254 | |||||||
| chr19:45017281 | G | T | 1 | a0001c0001t0001g0235 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.505-4772G>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45017281 | |||||||
| chr19:45017316 | A | G | 1 | a0001c0001t0001g0066 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.505-4737A>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45017316 | |||||||
| chr19:45017355 | G | A | 2 | a0001c0001t0001g0065 a0001c0001t0001g0073 |
2 | HG01069.hp2 HG01123.hp2 |
intron_variant | MODIFIER | c.505-4698G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45017355 | |||||||
| chr19:45017449 | T | TAAAAAAA others(1): Show |
149 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0014 others(146): Show |
151 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(148): Show |
intron_variant | MODIFIER | c.505-4597_505-4590d others(10): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr19 | 45017449 | ||||||
| chr19:45017449 | T | TAAAAAAA others(2): Show |
12 | a0001c0001t0001g0027 a0001c0001t0001g0197 a0001c0001t0001g0208 others(9): Show |
12 | HG01243.hp1 HG02145.hp2 HG04228.hp2 others(9): Show |
intron_variant | MODIFIER | c.505-4598_505-4590d others(11): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr19 | 45017449 | ||||||
| chr19:45017449 | T | TAAAAAAA others(3): Show |
59 | a0001c0001t0001g0006 a0001c0001t0001g0040 a0001c0001t0001g0042 others(56): Show |
60 | HG00408.hp2 HG00423.hp1 HG00673.hp1 others(57): Show |
intron_variant | MODIFIER | c.505-4599_505-4590d others(12): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr19 | 45017449 | ||||||
| chr19:45017449 | T | TAAAAAAA others(4): Show |
27 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0026 others(24): Show |
28 | HG00609.hp2 HG01109.hp2 HG01123.hp1 others(25): Show |
intron_variant | MODIFIER | c.505-4600_505-4590d others(13): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr19 | 45017449 | ||||||
| chr19:45017449 | T | TAAAAAAA others(5): Show |
6 | a0001c0001t0001g0035 a0001c0001t0001g0101 a0001c0001t0001g0276 others(3): Show |
6 | HG01891.hp1 HG02055.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.505-4601_505-4590d others(14): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr19 | 45017449 | ||||||
| chr19:45017449 | T | TAAAAAAA others(15): Show |
1 | a0001c0001t0001g0009 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.505-4590_505-4589i others(24): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr19 | 45017449 | ||||||
| chr19:45017449 | T | TAAAAAAA others(16): Show |
1 | a0001c0001t0001g0123 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.505-4590_505-4589i others(25): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr19 | 45017449 | ||||||
| chr19:45017449 | T | TAAAAAAA others(18): Show |
2 | a0001c0001t0001g0065 a0001c0001t0001g0073 |
2 | HG01069.hp2 HG01123.hp2 |
intron_variant | MODIFIER | c.505-4590_505-4589i others(27): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr19 | 45017449 | ||||||
| chr19:45017449 | T | TAAAAAAA others(20): Show |
4 | a0001c0001t0001g0270 a0001c0001t0001g0312 a0001c0001t0001g0313 others(1): Show |
4 | HG00733.hp2 HG02486.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.505-4590_505-4589i others(29): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr19 | 45017449 | ||||||
| chr19:45017449 | T | TAAAAAAA others(21): Show |
5 | a0001c0001t0001g0041 a0001c0001t0001g0161 a0001c0001t0001g0235 others(2): Show |
5 | HG02622.hp1 HG02970.hp1 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.505-4590_505-4589i others(30): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr19 | 45017449 | ||||||
| chr19:45017449 | T | TAAAAAAA others(22): Show |
1 | a0001c0001t0001g0160 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.505-4590_505-4589i others(31): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr19 | 45017449 | ||||||
| chr19:45017449 | T | TAAAAAAA others(24): Show |
2 | a0001c0001t0001g0128 a0001c0001t0001g0325 |
2 | HG02572.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.505-4590_505-4589i others(33): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr19 | 45017449 | ||||||
| chr19:45017449 | T | TAAAAAAA others(19): Show |
1 | a0001c0001t0001g0374 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.505-4590_505-4589i others(28): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr19 | 45017449 | ||||||
| chr19:45017450 | A | AAAAAAAA others(18): Show |
6 | a0001c0001t0001g0130 a0001c0001t0001g0138 a0001c0002t0001g0104 others(3): Show |
6 | HG02109.hp2 HG02451.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.505-4590_505-4589i others(27): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr19 | 45017450 | ||||||
| chr19:45017464 | C | A | 3 | a0001c0001t0001g0041 a0001c0001t0001g0128 a0001c0001t0001g0325 |
3 | HG02572.hp2 HG02622.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.505-4589C>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45017464 | |||||||
| chr19:45017603 | T | A | 1 | a0001c0001t0001g0289 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.505-4450T>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45017603 | |||||||
| chr19:45017663 | C | CT | 6 | a0001c0001t0001g0041 a0001c0001t0001g0128 a0001c0001t0001g0164 others(3): Show |
6 | HG01243.hp2 HG02572.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.505-4375dupT | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr19 | 45017663 | ||||||
| chr19:45017695 | C | T | 1 | a0001c0001t0001g0026 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.505-4358C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45017695 | |||||||
| chr19:45017701 | G | T | 8 | a0001c0001t0001g0034 a0001c0001t0001g0040 a0001c0001t0001g0079 others(5): Show |
8 | HG01109.hp2 HG02055.hp1 HG02683.hp2 others(5): Show |
intron_variant | MODIFIER | c.505-4352G>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45017701 | |||||||
| chr19:45017707 | G | C | 1 | a0001c0001t0001g0299 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.505-4346G>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45017707 | |||||||
| chr19:45017786 | C | T | 13 | a0001c0001t0001g0041 a0001c0001t0001g0065 a0001c0001t0001g0073 others(10): Show |
13 | HG01069.hp2 HG01123.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.505-4267C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45017786 | |||||||
| chr19:45017908 | G | A | 1 | a0001c0001t0001g0320 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.505-4145G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45017908 | |||||||
| chr19:45017935 | G | A | 1 | a0001c0001t0001g0087 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.505-4118G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45017935 | |||||||
| chr19:45018055 | T | G | 1 | a0001c0001t0001g0155 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.505-3998T>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45018055 | |||||||
| chr19:45018064 | C | T | 1 | a0001c0001t0001g0059 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.505-3989C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45018064 | |||||||
| chr19:45018168 | A | G | 278 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(275): Show |
282 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(279): Show |
intron_variant | MODIFIER | c.505-3885A>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45018168 | |||||||
| chr19:45018229 | C | T | 6 | a0001c0001t0001g0041 a0001c0001t0001g0065 a0001c0001t0001g0073 others(3): Show |
6 | HG01069.hp2 HG01123.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.505-3824C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45018229 | |||||||
| chr19:45018246 | T | C | 7 | a0001c0001t0001g0130 a0001c0001t0001g0138 a0001c0001t0001g0374 others(4): Show |
7 | HG02109.hp1 HG02109.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.505-3807T>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45018246 | |||||||
| chr19:45018342 | T | C | 1 | a0001c0001t0001g0358 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.505-3711T>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45018342 | |||||||
| chr19:45018352 | T | C | 264 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(261): Show |
268 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(265): Show |
intron_variant | MODIFIER | c.505-3701T>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45018352 | |||||||
| chr19:45018359 | G | A | 1 | a0001c0001t0001g0123 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.505-3694G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45018359 | |||||||
| chr19:45018372 | C | T | 1 | a0001c0001t0001g0123 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.505-3681C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45018372 | |||||||
| chr19:45018489 | C | CAG | 278 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(275): Show |
282 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(279): Show |
intron_variant | MODIFIER | c.505-3564_505-3563i others(4): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45018489 | |||||||
| chr19:45018507 | G | A | 1 | a0001c0001t0001g0123 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.505-3546G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45018507 | |||||||
| chr19:45018576 | C | T | 7 | a0001c0001t0001g0130 a0001c0001t0001g0138 a0001c0001t0001g0374 others(4): Show |
7 | HG02109.hp1 HG02109.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.505-3477C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45018576 | |||||||
| chr19:45018670 | A | AT | 3 | a0001c0001t0001g0026 a0001c0001t0001g0368 a0001c0001t0001g0369 |
3 | HG01243.hp1 HG03486.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.505-3380dupT | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr19 | 45018670 | ||||||
| chr19:45018673 | TA | T | 17 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0065 others(14): Show |
17 | HG00733.hp2 HG01069.hp2 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.505-3379delA | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45018673 | |||||||
| chr19:45018674 | A | T | 341 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(338): Show |
348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.505-3379A>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45018674 | |||||||
| chr19:45018790 | C | T | 1 | a0001c0001t0001g0311 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.505-3263C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45018790 | |||||||
| chr19:45018833 | C | T | 82 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0029 others(79): Show |
84 | HG00140.hp1 HG00408.hp1 HG00621.hp1 others(81): Show |
intron_variant | MODIFIER | c.505-3220C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45018833 | |||||||
| chr19:45018923 | G | A | 76 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0027 others(73): Show |
76 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.505-3130G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45018923 | |||||||
| chr19:45018923 | G | T | 7 | a0001c0001t0001g0130 a0001c0001t0001g0138 a0001c0001t0001g0374 others(4): Show |
7 | HG02109.hp1 HG02109.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.505-3130G>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45018923 | |||||||
| chr19:45018952 | C | T | 82 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0029 others(79): Show |
84 | HG00140.hp1 HG00408.hp1 HG00621.hp1 others(81): Show |
intron_variant | MODIFIER | c.505-3101C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45018952 | |||||||
| chr19:45018972 | T | A | 1 | a0001c0001t0001g0267 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.505-3081T>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45018972 | |||||||
| chr19:45018978 | A | G | 5 | a0001c0001t0001g0303 a0001c0001t0001g0355 a0001c0001t0002g0280 others(2): Show |
5 | HG03491.hp1 HG03654.hp2 HG04228.hp2 others(2): Show |
intron_variant | MODIFIER | c.505-3075A>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45018978 | |||||||
| chr19:45019031 | G | A | 3 | a0001c0001t0001g0034 a0001c0001t0001g0040 a0001c0001t0002g0280 |
3 | HG02738.hp2 HG03490.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.505-3022G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45019031 | |||||||
| chr19:45019054 | C | G | 1 | a0001c0001t0001g0276 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.505-2999C>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45019054 | |||||||
| chr19:45019062 | T | C | 1 | a0001c0001t0001g0175 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.505-2991T>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45019062 | |||||||
| chr19:45019147 | G | A | 5 | a0001c0001t0001g0303 a0001c0001t0001g0355 a0001c0001t0002g0280 others(2): Show |
5 | HG03491.hp1 HG03654.hp2 HG04228.hp2 others(2): Show |
intron_variant | MODIFIER | c.505-2906G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45019147 | |||||||
| chr19:45019194 | C | G | 6 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0235 others(3): Show |
6 | HG00733.hp2 HG01884.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.505-2859C>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45019194 | |||||||
| chr19:45019385 | C | T | 13 | a0001c0001t0001g0041 a0001c0001t0001g0065 a0001c0001t0001g0073 others(10): Show |
13 | HG01069.hp2 HG01123.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.505-2668C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45019385 | |||||||
| chr19:45019415 | C | G | 5 | a0001c0001t0001g0303 a0001c0001t0001g0355 a0001c0001t0002g0280 others(2): Show |
5 | HG03491.hp1 HG03654.hp2 HG04228.hp2 others(2): Show |
intron_variant | MODIFIER | c.505-2638C>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45019415 | |||||||
| chr19:45019459 | G | A | 2 | a0001c0001t0001g0368 a0001c0001t0001g0369 |
2 | HG01243.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.505-2594G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45019459 | |||||||
| chr19:45019474 | C | T | 76 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0027 others(73): Show |
76 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.505-2579C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45019474 | |||||||
| chr19:45019740 | C | G | 262 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(259): Show |
266 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(263): Show |
intron_variant | MODIFIER | c.505-2313C>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45019740 | |||||||
| chr19:45019801 | C | T | 4 | a0001c0001t0001g0144 a0001c0001t0001g0291 a0001c0001t0001g0292 others(1): Show |
4 | HG00673.hp1 HG02071.hp2 NA18952.hp1 others(1): Show |
intron_variant | MODIFIER | c.505-2252C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45019801 | |||||||
| chr19:45019803 | G | C | 1 | a0001c0001t0001g0181 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.505-2250G>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45019803 | |||||||
| chr19:45019869 | G | T | 69 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0035 others(66): Show |
70 | HG00408.hp2 HG00423.hp1 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.505-2184G>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45019869 | |||||||
| chr19:45019893 | TCTCAAAC others(34): Show |
T | 5 | a0001c0001t0001g0303 a0001c0001t0001g0355 a0001c0001t0002g0280 others(2): Show |
5 | HG03491.hp1 HG03654.hp2 HG04228.hp2 others(2): Show |
intron_variant | MODIFIER | c.505-2148_505-2108d others(43): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr19 | 45019893 | ||||||
| chr19:45020111 | T | G | 262 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(259): Show |
266 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(263): Show |
intron_variant | MODIFIER | c.505-1942T>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45020111 | |||||||
| chr19:45020144 | A | G | 3 | a0001c0001t0001g0041 a0001c0001t0001g0128 a0001c0001t0001g0325 |
3 | HG02572.hp2 HG02622.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.505-1909A>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45020144 | |||||||
| chr19:45020201 | G | A | 276 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(273): Show |
280 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(277): Show |
intron_variant | MODIFIER | c.505-1852G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45020201 | |||||||
| chr19:45020325 | G | A | 152 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(149): Show |
155 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(152): Show |
intron_variant | MODIFIER | c.505-1728G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45020325 | |||||||
| chr19:45020380 | C | T | 1 | a0001c0001t0001g0263 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.505-1673C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45020380 | |||||||
| chr19:45020402 | T | C | 3 | a0001c0001t0001g0041 a0001c0001t0001g0128 a0001c0001t0001g0325 |
3 | HG02572.hp2 HG02622.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.505-1651T>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45020402 | |||||||
| chr19:45020553 | C | CT | 176 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0009 others(173): Show |
178 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(175): Show |
intron_variant | MODIFIER | c.505-1478dupT | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr19 | 45020553 | ||||||
| chr19:45020553 | C | CTT | 83 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0013 others(80): Show |
85 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(82): Show |
intron_variant | MODIFIER | c.505-1479_505-1478d others(4): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr19 | 45020553 | ||||||
| chr19:45020553 | C | CTTT | 9 | a0001c0001t0001g0228 a0001c0001t0001g0255 a0001c0001t0001g0262 others(6): Show |
9 | HG00621.hp1 HG00733.hp1 HG00738.hp1 others(6): Show |
intron_variant | MODIFIER | c.505-1480_505-1478d others(5): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr19 | 45020553 | ||||||
| chr19:45020553 | CT | C | 6 | a0001c0001t0001g0025 a0001c0001t0001g0055 a0001c0001t0001g0067 others(3): Show |
6 | HG01261.hp2 HG01517.hp1 HG02602.hp1 others(3): Show |
intron_variant | MODIFIER | c.505-1478delT | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr19 | 45020553 | ||||||
| chr19:45020588 | C | T | 1 | a0001c0001t0001g0199 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.505-1465C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45020588 | |||||||
| chr19:45020593 | T | C | 1 | a0001c0001t0001g0063 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.505-1460T>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45020593 | |||||||
| chr19:45020621 | G | A | 1 | a0001c0001t0001g0114 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.505-1432G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45020621 | |||||||
| chr19:45020626 | T | C | 278 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(275): Show |
282 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(279): Show |
intron_variant | MODIFIER | c.505-1427T>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45020626 | |||||||
| chr19:45020643 | C | T | 8 | a0001c0001t0001g0007 a0001c0001t0001g0085 a0001c0001t0001g0127 others(5): Show |
9 | HG00438.hp2 HG01069.hp1 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.505-1410C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45020643 | |||||||
| chr19:45020747 | T | TG | 265 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(262): Show |
269 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(266): Show |
intron_variant | MODIFIER | c.505-1302dupG | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr19 | 45020747 | ||||||
| chr19:45020757 | C | T | 1 | a0001c0001t0003g0010 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.505-1296C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45020757 | |||||||
| chr19:45020778 | C | T | 262 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(259): Show |
266 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(263): Show |
intron_variant | MODIFIER | c.505-1275C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45020778 | |||||||
| chr19:45020837 | G | A | 1 | a0001c0001t0001g0176 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.505-1216G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45020837 | |||||||
| chr19:45020861 | C | T | 21 | a0001c0001t0001g0002 a0001c0001t0001g0034 a0001c0001t0001g0040 others(18): Show |
22 | HG01109.hp2 HG01891.hp1 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.505-1192C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45020861 | |||||||
| chr19:45020952 | A | T | 1 | a0001c0001t0001g0156 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.505-1101A>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45020952 | |||||||
| chr19:45020990 | T | C | 1 | a0001c0001t0001g0046 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.505-1063T>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45020990 | |||||||
| chr19:45021034 | G | T | 3 | a0001c0001t0001g0041 a0001c0001t0001g0128 a0001c0001t0001g0325 |
3 | HG02572.hp2 HG02622.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.505-1019G>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45021034 | |||||||
| chr19:45021047 | C | T | 1 | a0001c0001t0001g0072 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.505-1006C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45021047 | |||||||
| chr19:45021099 | C | T | 1 | a0001c0001t0001g0129 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.505-954C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45021099 | |||||||
| chr19:45021105 | C | T | 1 | a0001c0001t0001g0312 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.505-948C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45021105 | |||||||
| chr19:45021106 | G | A | 7 | a0001c0001t0001g0065 a0001c0001t0001g0073 a0001c0001t0001g0130 others(4): Show |
7 | HG01069.hp2 HG01123.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.505-947G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45021106 | |||||||
| chr19:45021186 | A | T | 26 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0039 others(23): Show |
27 | HG00673.hp1 HG01123.hp1 HG01891.hp1 others(24): Show |
intron_variant | MODIFIER | c.505-867A>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45021186 | |||||||
| chr19:45021244 | C | T | 1 | a0001c0006t0002g0322 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.505-809C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45021244 | |||||||
| chr19:45021295 | A | C | 29 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0026 others(26): Show |
30 | HG01109.hp2 HG01891.hp1 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.505-758A>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45021295 | |||||||
| chr19:45021335 | A | G | 1 | a0001c0001t0001g0147 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.505-718A>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45021335 | |||||||
| chr19:45021391 | G | A | 1 | a0001c0001t0001g0162 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.505-662G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45021391 | |||||||
| chr19:45021399 | G | T | 1 | a0001c0001t0001g0222 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.505-654G>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45021399 | |||||||
| chr19:45021421 | G | A | 71 | a0001c0001t0001g0014 a0001c0001t0001g0027 a0001c0001t0001g0028 others(68): Show |
71 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.505-632G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45021421 | |||||||
| chr19:45021456 | C | CA | 29 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(26): Show |
29 | HG00733.hp2 HG01081.hp1 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.505-578dupA | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr19 | 45021456 | ||||||
| chr19:45021456 | CA | C | 66 | a0001c0001t0001g0014 a0001c0001t0001g0026 a0001c0001t0001g0027 others(63): Show |
66 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.505-578delA | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr19 | 45021456 | ||||||
| chr19:45021573 | C | CT | 242 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(239): Show |
247 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(244): Show |
intron_variant | MODIFIER | c.505-459dupT | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr19 | 45021573 | ||||||
| chr19:45021573 | C | CTT | 12 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0018 others(9): Show |
12 | HG00438.hp1 HG01981.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.505-460_505-459dup others(2): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr19 | 45021573 | ||||||
| chr19:45021604 | A | T | 262 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(259): Show |
267 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(264): Show |
intron_variant | MODIFIER | c.505-449A>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45021604 | |||||||
| chr19:45021723 | C | T | 1 | a0001c0001t0001g0261 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.505-330C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45021723 | |||||||
| chr19:45021735 | G | A | 1 | a0001c0001t0001g0324 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.505-318G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45021735 | |||||||
| chr19:45021780 | A | G | 3 | a0001c0001t0001g0163 a0001c0001t0001g0370 a0001c0001t0002g0091 |
3 | HG01358.hp1 HG03704.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.505-273A>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45021780 | |||||||
| chr19:45021867 | G | A | 3 | a0001c0001t0001g0041 a0001c0001t0001g0128 a0001c0001t0001g0325 |
3 | HG02572.hp2 HG02622.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.505-186G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45021867 | |||||||
| chr19:45021911 | G | C | 1 | a0001c0001t0001g0138 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.505-142G>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45021911 | |||||||
| chr19:45021937 | C | T | 3 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0355 |
3 | HG02896.hp1 HG06807.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.505-116C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45021937 | |||||||
| chr19:45021949 | C | G | 1 | a0001c0001t0001g0203 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.505-104C>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 4/11 | chr19 | 45021949 | |||||||
| chr19:45022231 | G | A | 24 | a0001c0001t0001g0067 a0001c0001t0001g0074 a0001c0001t0001g0098 others(21): Show |
24 | HG00621.hp2 HG02040.hp2 HG02080.hp2 others(21): Show |
intron_variant | MODIFIER | c.662+21G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 5/11 | chr19 | 45022231 | |||||||
| chr19:45022547 | CT | C | 266 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(263): Show |
272 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(269): Show |
intron_variant | MODIFIER | c.662+354delT | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 45022547 | ||||||
| chr19:45022547 | CTT | C | 15 | a0001c0001t0001g0112 a0001c0001t0001g0123 a0001c0001t0001g0128 others(12): Show |
15 | HG01123.hp1 HG01261.hp2 HG01433.hp2 others(12): Show |
intron_variant | MODIFIER | c.662+353_662+354del others(2): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 45022547 | ||||||
| chr19:45022663 | C | T | 4 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0189 others(1): Show |
4 | HG01081.hp1 HG01192.hp2 HG01255.hp2 others(1): Show |
intron_variant | MODIFIER | c.662+453C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 5/11 | chr19 | 45022663 | |||||||
| chr19:45022774 | G | C | 2 | a0001c0001t0001g0128 a0001c0001t0001g0325 |
2 | HG02572.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.662+564G>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 5/11 | chr19 | 45022774 | |||||||
| chr19:45023393 | T | TTTCC | 52 | a0001c0001t0001g0001 a0001c0001t0001g0027 a0001c0001t0001g0028 others(49): Show |
53 | HG00544.hp2 HG00609.hp1 HG01069.hp2 others(50): Show |
intron_variant | MODIFIER | c.662+1220_662+1223d others(6): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 45023393 | ||||||
| chr19:45023393 | T | TTTCCTTC others(1): Show |
43 | a0001c0001t0001g0015 a0001c0001t0001g0053 a0001c0001t0001g0058 others(40): Show |
43 | HG00099.hp1 HG00621.hp2 HG00733.hp1 others(40): Show |
intron_variant | MODIFIER | c.662+1216_662+1223d others(10): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 45023393 | ||||||
| chr19:45023393 | T | TTTCCTTC others(5): Show |
42 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0014 others(39): Show |
43 | HG00544.hp1 HG00558.hp1 HG00558.hp2 others(40): Show |
intron_variant | MODIFIER | c.662+1212_662+1223d others(14): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 45023393 | ||||||
| chr19:45023393 | T | TTTCCTTC others(9): Show |
11 | a0001c0001t0001g0041 a0001c0001t0001g0103 a0001c0001t0001g0129 others(8): Show |
11 | HG00639.hp2 HG01257.hp1 HG01361.hp2 others(8): Show |
intron_variant | MODIFIER | c.662+1208_662+1223d others(18): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 45023393 | ||||||
| chr19:45023393 | T | TTTCCTTC others(13): Show |
1 | a0001c0001t0001g0034 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.662+1204_662+1223d others(22): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 45023393 | ||||||
| chr19:45023393 | T | TTTCCTTC others(17): Show |
1 | a0001c0001t0001g0155 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.662+1200_662+1223d others(26): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 45023393 | ||||||
| chr19:45023393 | TTTCC | T | 19 | a0001c0001t0001g0042 a0001c0001t0001g0054 a0001c0001t0001g0062 others(16): Show |
19 | HG00140.hp1 HG01109.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.662+1220_662+1223d others(6): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 45023393 | ||||||
| chr19:45023434 | G | A | 4 | a0001c0001t0001g0087 a0001c0001t0001g0272 a0001c0001t0001g0312 others(1): Show |
4 | HG02257.hp2 HG02486.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.662+1224G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 5/11 | chr19 | 45023434 | |||||||
| chr19:45023466 | C | T | 1 | a0001c0001t0002g0117 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.662+1256C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 5/11 | chr19 | 45023466 | |||||||
| chr19:45023626 | G | C | 1 | a0001c0001t0001g0220 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.662+1416G>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 5/11 | chr19 | 45023626 | |||||||
| chr19:45023639 | C | T | 19 | a0001c0001t0001g0030 a0001c0001t0001g0057 a0001c0001t0001g0119 others(16): Show |
19 | HG00621.hp1 HG02135.hp1 NA18612.hp2 others(16): Show |
intron_variant | MODIFIER | c.662+1429C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 5/11 | chr19 | 45023639 | |||||||
| chr19:45023640 | G | A | 1 | a0001c0001t0001g0038 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.662+1430G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 5/11 | chr19 | 45023640 | |||||||
| chr19:45023676 | G | A | 3 | a0001c0001t0001g0123 a0001c0001t0001g0155 a0001c0001t0001g0307 |
3 | HG01261.hp2 HG01433.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.662+1466G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 5/11 | chr19 | 45023676 | |||||||
| chr19:45023740 | C | CT | 72 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0026 others(69): Show |
73 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.662+1558dupT | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 45023740 | ||||||
| chr19:45023740 | C | CTT | 20 | a0001c0001t0001g0015 a0001c0001t0001g0034 a0001c0001t0001g0048 others(17): Show |
20 | HG00735.hp1 HG01192.hp1 HG01361.hp2 others(17): Show |
intron_variant | MODIFIER | c.662+1557_662+1558d others(4): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 45023740 | ||||||
| chr19:45023740 | CT | C | 158 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(155): Show |
162 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(159): Show |
intron_variant | MODIFIER | c.662+1558delT | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 45023740 | ||||||
| chr19:45023740 | CTT | C | 12 | a0001c0001t0001g0025 a0001c0001t0001g0041 a0001c0001t0001g0060 others(9): Show |
12 | HG02004.hp2 HG02055.hp2 HG02132.hp1 others(9): Show |
intron_variant | MODIFIER | c.662+1557_662+1558d others(4): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 45023740 | ||||||
| chr19:45023791 | C | A | 1 | a0001c0001t0003g0256 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.663-1538C>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 5/11 | chr19 | 45023791 | |||||||
| chr19:45023880 | AGCTGGGA others(218): Show |
A | 1 | a0001c0001t0001g0042 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.663-1432_663-1208d others(2): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 45023880 | ||||||
| chr19:45023915 | TAATTTTT others(85): Show |
T | 272 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(269): Show |
277 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(274): Show |
intron_variant | MODIFIER | c.663-1321_663-1230d others(94): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 45023915 | ||||||
| chr19:45023940 | GGGGTTTC others(84): Show |
G | 1 | a0001c0001t0002g0363 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.663-1385_663-1295d others(93): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 45023940 | ||||||
| chr19:45024026 | A | G | 1 | a0001c0001t0001g0361 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.663-1303A>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 5/11 | chr19 | 45024026 | |||||||
| chr19:45024184 | C | T | 3 | a0001c0001t0001g0123 a0001c0001t0001g0155 a0001c0001t0001g0307 |
3 | HG01261.hp2 HG01433.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.663-1145C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 5/11 | chr19 | 45024184 | |||||||
| chr19:45024223 | G | A | 1 | a0001c0001t0001g0042 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.663-1106G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 5/11 | chr19 | 45024223 | |||||||
| chr19:45024310 | C | T | 261 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(258): Show |
266 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(263): Show |
intron_variant | MODIFIER | c.663-1019C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 5/11 | chr19 | 45024310 | |||||||
| chr19:45024335 | T | G | 1 | a0001c0001t0002g0363 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.663-994T>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 5/11 | chr19 | 45024335 | |||||||
| chr19:45024371 | C | G | 1 | a0001c0001t0001g0026 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.663-958C>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 5/11 | chr19 | 45024371 | |||||||
| chr19:45024383 | C | G | 6 | a0001c0001t0001g0137 a0001c0001t0001g0235 a0001c0001t0001g0270 others(3): Show |
6 | HG00733.hp2 HG01243.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.663-946C>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 5/11 | chr19 | 45024383 | |||||||
| chr19:45024531 | C | G | 2 | a0001c0001t0001g0334 a0001c0001t0001g0335 |
2 | HG02523.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.663-798C>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 5/11 | chr19 | 45024531 | |||||||
| chr19:45024549 | C | A | 1 | a0001c0001t0001g0042 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.663-780C>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 5/11 | chr19 | 45024549 | |||||||
| chr19:45024589 | C | T | 2 | a0001c0001t0001g0009 a0001c0001t0001g0177 |
2 | NA19043.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.663-740C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 5/11 | chr19 | 45024589 | |||||||
| chr19:45024598 | G | A | 6 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0002t0001g0104 others(3): Show |
6 | HG02109.hp2 HG02451.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.663-731G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 5/11 | chr19 | 45024598 | |||||||
| chr19:45024699 | G | A | 3 | a0001c0001t0001g0116 a0001c0001t0001g0186 a0001c0003t0001g0253 |
3 | HG03239.hp2 HG03654.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.663-630G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 5/11 | chr19 | 45024699 | |||||||
| chr19:45024900 | C | T | 4 | a0001c0001t0001g0112 a0001c0001t0001g0352 a0001c0001t0001g0353 others(1): Show |
4 | HG01123.hp1 HG02055.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.663-429C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 5/11 | chr19 | 45024900 | |||||||
| chr19:45024929 | G | A | 4 | a0001c0001t0001g0112 a0001c0001t0001g0352 a0001c0001t0001g0353 others(1): Show |
4 | HG01123.hp1 HG02055.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.663-400G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 5/11 | chr19 | 45024929 | |||||||
| chr19:45025040 | G | A | 4 | a0001c0001t0001g0041 a0001c0001t0001g0141 a0001c0001t0001g0142 others(1): Show |
4 | HG02622.hp1 HG02896.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.663-289G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 5/11 | chr19 | 45025040 | |||||||
| chr19:45025107 | C | T | 1 | a0001c0001t0001g0173 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.663-222C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 5/11 | chr19 | 45025107 | |||||||
| chr19:45025111 | G | A | 1 | a0001c0001t0001g0096 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.663-218G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 5/11 | chr19 | 45025111 | |||||||
| chr19:45025156 | C | T | 2 | a0001c0001t0001g0367 a0001c0001t0001g0374 |
2 | HG02109.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.663-173C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 5/11 | chr19 | 45025156 | |||||||
| chr19:45025181 | C | A | 1 | a0001c0001t0001g0293 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.663-148C>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 5/11 | chr19 | 45025181 | |||||||
| chr19:45025253 | C | T | 1 | a0001c0001t0001g0111 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.663-76C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 5/11 | chr19 | 45025253 | |||||||
| chr19:45025292 | C | T | 4 | a0001c0001t0001g0112 a0001c0001t0001g0352 a0001c0001t0001g0353 others(1): Show |
4 | HG01123.hp1 HG02055.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.663-37C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 5/11 | chr19 | 45025292 | |||||||
| chr19:45025451 | C | A | 1 | a0001c0001t0001g0119 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.754+31C>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 6/11 | chr19 | 45025451 | |||||||
| chr19:45025532 | C | A | 1 | a0001c0001t0001g0220 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.755-74C>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 6/11 | chr19 | 45025532 | |||||||
| chr19:45025541 | T | C | 188 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(185): Show |
192 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(189): Show |
intron_variant | MODIFIER | c.755-65T>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 6/11 | chr19 | 45025541 | |||||||
| chr19:45025575 | A | C | 1 | a0001c0001t0001g0081 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.755-31A>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 6/11 | chr19 | 45025575 | |||||||
| chr19:45026449 | G | A | 186 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(183): Show |
190 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(187): Show |
intron_variant | MODIFIER | c.886+712G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 7/11 | chr19 | 45026449 | |||||||
| chr19:45026449 | G | C | 1 | a0001c0001t0001g0185 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.886+712G>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 7/11 | chr19 | 45026449 | |||||||
| chr19:45026553 | G | GA | 260 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(257): Show |
265 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(262): Show |
intron_variant | MODIFIER | c.886+825dupA | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr19 | 45026553 | ||||||
| chr19:45026567 | A | G | 1 | a0001c0001t0001g0026 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.886+830A>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 7/11 | chr19 | 45026567 | |||||||
| chr19:45026589 | G | A | 2 | a0001c0001t0001g0058 a0001c0001t0001g0066 |
2 | HG03710.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.886+852G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 7/11 | chr19 | 45026589 | |||||||
| chr19:45026677 | G | C | 1 | a0001c0001t0001g0022 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.886+940G>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 7/11 | chr19 | 45026677 | |||||||
| chr19:45026748 | A | G | 188 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(185): Show |
192 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(189): Show |
intron_variant | MODIFIER | c.886+1011A>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 7/11 | chr19 | 45026748 | |||||||
| chr19:45026956 | G | A | 1 | a0001c0001t0001g0044 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.886+1219G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 7/11 | chr19 | 45026956 | |||||||
| chr19:45027034 | C | A | 3 | a0001c0001t0001g0123 a0001c0001t0001g0155 a0001c0001t0001g0307 |
3 | HG01261.hp2 HG01433.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.886+1297C>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 7/11 | chr19 | 45027034 | |||||||
| chr19:45027084 | T | A | 1 | a0001c0001t0001g0057 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.886+1347T>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 7/11 | chr19 | 45027084 | |||||||
| chr19:45027093 | C | T | 67 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0015 others(64): Show |
68 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(65): Show |
intron_variant | MODIFIER | c.886+1356C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 7/11 | chr19 | 45027093 | |||||||
| chr19:45027181 | C | G | 1 | a0001c0001t0002g0330 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.886+1444C>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 7/11 | chr19 | 45027181 | |||||||
| chr19:45027219 | C | T | 1 | a0001c0001t0003g0010 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.886+1482C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 7/11 | chr19 | 45027219 | |||||||
| chr19:45027232 | C | CA | 190 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(187): Show |
194 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(191): Show |
intron_variant | MODIFIER | c.886+1510dupA | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr19 | 45027232 | ||||||
| chr19:45027232 | C | CAA | 65 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0015 others(62): Show |
66 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.886+1509_886+1510d others(4): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr19 | 45027232 | ||||||
| chr19:45027235 | A | C | 1 | a0001c0001t0001g0216 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.886+1498A>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 7/11 | chr19 | 45027235 | |||||||
| chr19:45027257 | C | T | 1 | a0001c0001t0001g0044 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.886+1520C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 7/11 | chr19 | 45027257 | |||||||
| chr19:45027294 | A | G | 273 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(270): Show |
278 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(275): Show |
intron_variant | MODIFIER | c.886+1557A>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 7/11 | chr19 | 45027294 | |||||||
| chr19:45027313 | C | T | 1 | a0001c0001t0001g0026 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.887-1575C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 7/11 | chr19 | 45027313 | |||||||
| chr19:45027350 | TGGCTGCA others(4): Show |
T | 1 | a0001c0001t0001g0057 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.887-1535_887-1525d others(13): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr19 | 45027350 | ||||||
| chr19:45027466 | C | T | 2 | a0001c0001t0001g0128 a0001c0001t0001g0325 |
2 | HG02572.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.887-1422C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 7/11 | chr19 | 45027466 | |||||||
| chr19:45027678 | C | T | 1 | a0001c0001t0001g0129 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.887-1210C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 7/11 | chr19 | 45027678 | |||||||
| chr19:45027794 | T | C | 4 | a0001c0001t0001g0112 a0001c0001t0001g0352 a0001c0001t0001g0353 others(1): Show |
4 | HG01123.hp1 HG02055.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.887-1094T>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 7/11 | chr19 | 45027794 | |||||||
| chr19:45027905 | G | C | 8 | a0001c0001t0001g0036 a0001c0001t0001g0110 a0001c0001t0001g0132 others(5): Show |
8 | HG00738.hp2 HG01074.hp2 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.887-983G>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 7/11 | chr19 | 45027905 | |||||||
| chr19:45028258 | G | A | 5 | a0001c0001t0001g0129 a0001c0002t0001g0104 a0001c0002t0001g0131 others(2): Show |
5 | HG02109.hp2 HG02451.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.887-630G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 7/11 | chr19 | 45028258 | |||||||
| chr19:45028262 | T | G | 1 | a0001c0001t0001g0108 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.887-626T>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 7/11 | chr19 | 45028262 | |||||||
| chr19:45028336 | GT | G | 4 | a0001c0001t0001g0041 a0001c0001t0001g0141 a0001c0001t0001g0142 others(1): Show |
4 | HG02622.hp1 HG02896.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.887-548delT | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr19 | 45028336 | ||||||
| chr19:45028348 | T | G | 1 | a0001c0001t0001g0274 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.887-540T>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 7/11 | chr19 | 45028348 | |||||||
| chr19:45028360 | GT | G | 5 | a0001c0001t0001g0001 a0001c0001t0001g0045 a0001c0001t0001g0049 others(2): Show |
6 | HG01358.hp2 HG03490.hp1 HG03492.hp2 others(3): Show |
intron_variant | MODIFIER | c.887-522delT | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr19 | 45028360 | ||||||
| chr19:45028603 | G | A | 1 | a0001c0001t0001g0040 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.887-285G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 7/11 | chr19 | 45028603 | |||||||
| chr19:45028624 | A | G | 5 | a0001c0001t0001g0129 a0001c0002t0001g0104 a0001c0002t0001g0131 others(2): Show |
5 | HG02109.hp2 HG02451.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.887-264A>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 7/11 | chr19 | 45028624 | |||||||
| chr19:45028637 | G | C | 1 | a0001c0001t0001g0163 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.887-251G>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 7/11 | chr19 | 45028637 | |||||||
| chr19:45028680 | G | A | 4 | a0001c0001t0001g0144 a0001c0001t0001g0289 a0001c0001t0001g0291 others(1): Show |
4 | HG00673.hp1 NA18952.hp1 NA18997.hp2 others(1): Show |
intron_variant | MODIFIER | c.887-208G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 7/11 | chr19 | 45028680 | |||||||
| chr19:45028751 | G | T | 188 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(185): Show |
192 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(189): Show |
intron_variant | MODIFIER | c.887-137G>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 7/11 | chr19 | 45028751 | |||||||
| chr19:45029187 | C | T | 13 | a0001c0001t0001g0035 a0001c0001t0001g0037 a0001c0001t0001g0038 others(10): Show |
13 | HG00733.hp2 HG01123.hp1 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.991+195C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 8/11 | chr19 | 45029187 | |||||||
| chr19:45029188 | G | A | 1 | a0001c0001t0001g0059 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.991+196G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 8/11 | chr19 | 45029188 | |||||||
| chr19:45029201 | G | A | 1 | a0001c0001t0001g0026 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.991+209G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 8/11 | chr19 | 45029201 | |||||||
| chr19:45029317 | C | T | 1 | a0001c0001t0001g0152 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.991+325C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 8/11 | chr19 | 45029317 | |||||||
| chr19:45029367 | A | G | 3 | a0001c0001t0001g0026 a0001c0001t0001g0128 a0001c0001t0001g0325 |
3 | HG02572.hp2 HG03486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.991+375A>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 8/11 | chr19 | 45029367 | |||||||
| chr19:45029389 | T | C | 1 | a0001c0001t0001g0069 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.991+397T>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 8/11 | chr19 | 45029389 | |||||||
| chr19:45029576 | G | T | 8 | a0001c0001t0001g0087 a0001c0001t0001g0123 a0001c0001t0001g0155 others(5): Show |
8 | HG01261.hp2 HG01433.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.991+584G>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 8/11 | chr19 | 45029576 | |||||||
| chr19:45029939 | G | A | 2 | a0001c0001t0001g0155 a0001c0001t0001g0307 |
2 | HG01261.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.991+947G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 8/11 | chr19 | 45029939 | |||||||
| chr19:45029965 | C | T | 8 | a0001c0001t0001g0087 a0001c0001t0001g0123 a0001c0001t0001g0155 others(5): Show |
8 | HG01261.hp2 HG01433.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.991+973C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 8/11 | chr19 | 45029965 | |||||||
| chr19:45029996 | T | C | 1 | a0001c0001t0001g0026 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.991+1004T>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 8/11 | chr19 | 45029996 | |||||||
| chr19:45030142 | G | A | 4 | a0001c0001t0001g0041 a0001c0001t0001g0141 a0001c0001t0001g0142 others(1): Show |
4 | HG02622.hp1 HG02896.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.991+1150G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 8/11 | chr19 | 45030142 | |||||||
| chr19:45030185 | A | G | 1 | a0001c0001t0001g0026 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.991+1193A>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 8/11 | chr19 | 45030185 | |||||||
| chr19:45030191 | C | T | 1 | a0001c0001t0001g0114 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.991+1199C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 8/11 | chr19 | 45030191 | |||||||
| chr19:45030303 | T | C | 1 | a0001c0001t0001g0051 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.991+1311T>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 8/11 | chr19 | 45030303 | |||||||
| chr19:45030370 | A | C | 1 | a0001c0001t0001g0255 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.991+1378A>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 8/11 | chr19 | 45030370 | |||||||
| chr19:45030477 | T | A | 1 | a0001c0001t0001g0129 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.991+1485T>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 8/11 | chr19 | 45030477 | |||||||
| chr19:45030759 | C | T | 1 | a0001c0001t0001g0129 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.991+1767C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 8/11 | chr19 | 45030759 | |||||||
| chr19:45030783 | C | T | 186 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(183): Show |
190 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(187): Show |
intron_variant | MODIFIER | c.992-1751C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 8/11 | chr19 | 45030783 | |||||||
| chr19:45030865 | G | C | 1 | a0001c0001t0001g0026 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.992-1669G>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 8/11 | chr19 | 45030865 | |||||||
| chr19:45031038 | A | G | 2 | a0001c0001t0001g0178 a0001c0001t0001g0216 |
2 | NA19000.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.992-1496A>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 8/11 | chr19 | 45031038 | |||||||
| chr19:45031102 | A | G | 5 | a0001c0001t0001g0115 a0001c0001t0001g0137 a0001c0001t0001g0235 others(2): Show |
5 | HG00733.hp2 HG00741.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.992-1432A>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 8/11 | chr19 | 45031102 | |||||||
| chr19:45031189 | C | T | 1 | a0001c0001t0002g0043 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.992-1345C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 8/11 | chr19 | 45031189 | |||||||
| chr19:45031201 | T | G | 4 | a0001c0001t0001g0041 a0001c0001t0001g0141 a0001c0001t0001g0142 others(1): Show |
4 | HG02622.hp1 HG02896.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.992-1333T>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 8/11 | chr19 | 45031201 | |||||||
| chr19:45031231 | G | A | 5 | a0001c0001t0001g0129 a0001c0002t0001g0104 a0001c0002t0001g0131 others(2): Show |
5 | HG02109.hp2 HG02451.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.992-1303G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 8/11 | chr19 | 45031231 | |||||||
| chr19:45031265 | A | T | 4 | a0001c0001t0001g0041 a0001c0001t0001g0141 a0001c0001t0001g0142 others(1): Show |
4 | HG02622.hp1 HG02896.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.992-1269A>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 8/11 | chr19 | 45031265 | |||||||
| chr19:45031587 | T | G | 1 | a0001c0004t0001g0241 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.992-947T>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 8/11 | chr19 | 45031587 | |||||||
| chr19:45031609 | T | C | 1 | a0001c0001t0001g0301 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.992-925T>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 8/11 | chr19 | 45031609 | |||||||
| chr19:45031679 | C | A | 1 | a0001c0001t0001g0343 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.992-855C>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 8/11 | chr19 | 45031679 | |||||||
| chr19:45031700 | T | C | 1 | a0001c0001t0001g0118 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.992-834T>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 8/11 | chr19 | 45031700 | |||||||
| chr19:45031724 | T | C | 3 | a0001c0001t0001g0046 a0001c0001t0001g0070 a0001c0001t0001g0276 |
3 | HG03130.hp1 HG03453.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.992-810T>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 8/11 | chr19 | 45031724 | |||||||
| chr19:45031736 | C | T | 67 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(64): Show |
70 | HG00140.hp2 HG00323.hp1 HG00621.hp2 others(67): Show |
intron_variant | MODIFIER | c.992-798C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 8/11 | chr19 | 45031736 | |||||||
| chr19:45031786 | C | T | 10 | a0001c0001t0001g0087 a0001c0001t0001g0123 a0001c0001t0001g0130 others(7): Show |
10 | HG01261.hp2 HG01433.hp2 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.992-748C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 8/11 | chr19 | 45031786 | |||||||
| chr19:45031787 | G | A | 1 | a0001c0001t0001g0153 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.992-747G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 8/11 | chr19 | 45031787 | |||||||
| chr19:45031827 | C | T | 7 | a0001c0001t0001g0050 a0001c0001t0001g0076 a0001c0001t0001g0202 others(4): Show |
7 | HG02145.hp2 HG02258.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.992-707C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 8/11 | chr19 | 45031827 | |||||||
| chr19:45031973 | T | C | 1 | a0001c0001t0001g0240 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.992-561T>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 8/11 | chr19 | 45031973 | |||||||
| chr19:45032048 | C | T | 3 | a0001c0001t0001g0169 a0001c0001t0001g0259 a0001c0001t0001g0347 |
3 | NA18612.hp2 NA19057.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.992-486C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 8/11 | chr19 | 45032048 | |||||||
| chr19:45032052 | G | A | 160 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0012 others(157): Show |
162 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.992-482G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 8/11 | chr19 | 45032052 | |||||||
| chr19:45032072 | T | C | 2 | a0001c0001t0001g0135 a0001c0001t0001g0318 |
2 | HG01099.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.992-462T>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 8/11 | chr19 | 45032072 | |||||||
| chr19:45032129 | G | A | 1 | a0001c0001t0001g0176 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.992-405G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 8/11 | chr19 | 45032129 | |||||||
| chr19:45032258 | C | A | 14 | a0001c0001t0001g0041 a0001c0001t0001g0087 a0001c0001t0001g0141 others(11): Show |
14 | HG01884.hp2 HG02109.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.992-276C>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 8/11 | chr19 | 45032258 | |||||||
| chr19:45032313 | G | A | 6 | a0001c0001t0001g0190 a0001c0001t0001g0191 a0001c0001t0001g0192 others(3): Show |
6 | HG02109.hp1 HG02647.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.992-221G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 8/11 | chr19 | 45032313 | |||||||
| chr19:45032373 | C | G | 1 | a0001c0001t0001g0308 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.992-161C>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 8/11 | chr19 | 45032373 | |||||||
| chr19:45032402 | G | C | 10 | a0001c0001t0001g0087 a0001c0001t0001g0123 a0001c0001t0001g0130 others(7): Show |
10 | HG01261.hp2 HG01433.hp2 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.992-132G>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 8/11 | chr19 | 45032402 | |||||||
| chr19:45032414 | CA | C | 187 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(184): Show |
192 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(189): Show |
intron_variant | MODIFIER | c.992-108delA | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr19 | 45032414 | ||||||
| chr19:45032430 | T | A | 1 | a0001c0001t0001g0185 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.992-104T>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 8/11 | chr19 | 45032430 | |||||||
| chr19:45032778 | C | G | 156 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(153): Show |
159 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.1207+29C>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 9/11 | chr19 | 45032778 | |||||||
| chr19:45032803 | T | C | 3 | a0001c0001t0001g0012 a0001c0001t0003g0010 a0001c0001t0003g0245 |
3 | HG01192.hp2 HG01361.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.1207+54T>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 9/11 | chr19 | 45032803 | |||||||
| chr19:45032912 | T | C | 2 | a0001c0001t0001g0089 a0001c0001t0001g0249 |
2 | NA18973.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.1207+163T>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 9/11 | chr19 | 45032912 | |||||||
| chr19:45032935 | C | T | 1 | a0001c0001t0001g0255 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1207+186C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 9/11 | chr19 | 45032935 | |||||||
| chr19:45032938 | T | C | 1 | a0001c0001t0001g0187 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1207+189T>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 9/11 | chr19 | 45032938 | |||||||
| chr19:45032957 | T | A | 22 | a0001c0001t0001g0035 a0001c0001t0001g0037 a0001c0001t0001g0038 others(19): Show |
22 | HG00733.hp2 HG01109.hp2 HG01123.hp1 others(19): Show |
intron_variant | MODIFIER | c.1207+208T>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 9/11 | chr19 | 45032957 | |||||||
| chr19:45033020 | C | T | 1 | a0001c0001t0002g0091 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1207+271C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 9/11 | chr19 | 45033020 | |||||||
| chr19:45033267 | C | G | 1 | a0001c0001t0001g0359 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1207+518C>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 9/11 | chr19 | 45033267 | |||||||
| chr19:45033275 | G | A | 1 | a0001c0001t0001g0370 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1207+526G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 9/11 | chr19 | 45033275 | |||||||
| chr19:45033315 | C | A | 13 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(10): Show |
13 | HG01943.hp1 HG01952.hp2 HG01981.hp1 others(10): Show |
intron_variant | MODIFIER | c.1207+566C>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 9/11 | chr19 | 45033315 | |||||||
| chr19:45033382 | C | A | 1 | a0001c0001t0001g0346 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1207+633C>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 9/11 | chr19 | 45033382 | |||||||
| chr19:45033477 | G | A | 1 | a0001c0001t0001g0042 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1207+728G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 9/11 | chr19 | 45033477 | |||||||
| chr19:45033488 | C | T | 1 | a0001c0001t0001g0052 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1207+739C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 9/11 | chr19 | 45033488 | |||||||
| chr19:45033610 | G | A | 5 | a0001c0001t0001g0077 a0001c0001t0001g0096 a0001c0001t0001g0358 others(2): Show |
5 | HG02145.hp1 HG02630.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1208-634G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 9/11 | chr19 | 45033610 | |||||||
| chr19:45033750 | T | C | 5 | a0001c0001t0001g0039 a0001c0001t0001g0041 a0001c0001t0001g0141 others(2): Show |
5 | HG02622.hp1 HG02896.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1208-494T>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 9/11 | chr19 | 45033750 | |||||||
| chr19:45033762 | C | T | 26 | a0001c0001t0001g0039 a0001c0001t0001g0041 a0001c0001t0001g0042 others(23): Show |
26 | HG01261.hp2 HG01433.hp2 HG01884.hp2 others(23): Show |
intron_variant | MODIFIER | c.1208-482C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 9/11 | chr19 | 45033762 | |||||||
| chr19:45033763 | G | A | 1 | a0001c0001t0001g0106 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1208-481G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 9/11 | chr19 | 45033763 | |||||||
| chr19:45033853 | C | CT | 7 | a0001c0001t0001g0077 a0001c0001t0001g0096 a0001c0001t0001g0128 others(4): Show |
7 | HG02145.hp1 HG02572.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1208-388dupT | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr19 | 45033853 | ||||||
| chr19:45033857 | A | T | 26 | a0001c0001t0001g0039 a0001c0001t0001g0041 a0001c0001t0001g0042 others(23): Show |
26 | HG01261.hp2 HG01433.hp2 HG01884.hp2 others(23): Show |
intron_variant | MODIFIER | c.1208-387A>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 9/11 | chr19 | 45033857 | |||||||
| chr19:45033858 | A | T | 20 | a0001c0001t0001g0009 a0001c0001t0001g0039 a0001c0001t0001g0041 others(17): Show |
20 | HG01261.hp2 HG01433.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.1208-386A>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 9/11 | chr19 | 45033858 | |||||||
| chr19:45033859 | A | T | 5 | a0001c0001t0001g0009 a0001c0001t0001g0042 a0001c0002t0001g0131 others(2): Show |
5 | HG02109.hp2 HG02451.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1208-385A>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 9/11 | chr19 | 45033859 | |||||||
| chr19:45033912 | C | T | 4 | a0001c0002t0001g0104 a0001c0002t0001g0131 a0001c0002t0001g0133 others(1): Show |
4 | HG02109.hp2 HG02451.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1208-332C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 9/11 | chr19 | 45033912 | |||||||
| chr19:45034019 | C | T | 1 | a0001c0001t0001g0287 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1208-225C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 9/11 | chr19 | 45034019 | |||||||
| chr19:45034159 | A | AAAAT | 24 | a0001c0001t0001g0009 a0001c0001t0001g0039 a0001c0001t0001g0041 others(21): Show |
24 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(21): Show |
intron_variant | MODIFIER | c.1208-61_1208-58dup others(4): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr19 | 45034159 | ||||||
| chr19:45034159 | AAAAT | A | 158 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(155): Show |
161 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.1208-61_1208-58del others(4): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr19 | 45034159 | ||||||
| chr19:45034565 | G | C | 2 | a0001c0001t0001g0002 a0001c0001t0001g0092 |
3 | HG02886.hp1 HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1354+37G>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 11/11 | chr19 | 45034565 | |||||||
| chr19:45034575 | G | A | 1 | a0001c0001t0001g0108 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1354+47G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 11/11 | chr19 | 45034575 | |||||||
| chr19:45034703 | C | T | 1 | a0001c0001t0001g0130 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1354+175C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 11/11 | chr19 | 45034703 | |||||||
| chr19:45034797 | A | G | 1 | a0001c0001t0001g0092 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1354+269A>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 11/11 | chr19 | 45034797 | |||||||
| chr19:45034841 | TC | T | 15 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(12): Show |
15 | HG00423.hp2 HG01943.hp1 HG01952.hp2 others(12): Show |
intron_variant | MODIFIER | c.1354+314delC | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 11/11 | chr19 | 45034841 | |||||||
| chr19:45034842 | C | T | 1 | a0001c0001t0001g0113 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1354+314C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 11/11 | chr19 | 45034842 | |||||||
| chr19:45034943 | C | T | 3 | a0001c0001t0001g0123 a0001c0001t0001g0155 a0001c0001t0001g0307 |
3 | HG01261.hp2 HG01433.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1354+415C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 11/11 | chr19 | 45034943 | |||||||
| chr19:45035447 | G | T | 2 | a0001c0001t0001g0128 a0001c0001t0001g0325 |
2 | HG02572.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1354+919G>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 11/11 | chr19 | 45035447 | |||||||
| chr19:45035539 | C | CAACAACA others(15): Show |
4 | a0001c0001t0001g0077 a0001c0001t0001g0096 a0001c0001t0001g0358 others(1): Show |
4 | HG02145.hp1 HG02630.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.1354+1013_1354+101 others(26): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr19 | 45035539 | ||||||
| chr19:45035539 | C | CAACAACA others(18): Show |
1 | a0001c0001t0001g0360 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1354+1013_1354+101 others(29): Show |
RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr19 | 45035539 | ||||||
| chr19:45035576 | C | T | 1 | a0001c0001t0001g0250 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1354+1048C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 11/11 | chr19 | 45035576 | |||||||
| chr19:45035745 | G | T | 1 | a0001c0001t0001g0129 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1354+1217G>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 11/11 | chr19 | 45035745 | |||||||
| chr19:45035878 | T | C | 1 | a0001c0001t0001g0042 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1354+1350T>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 11/11 | chr19 | 45035878 | |||||||
| chr19:45035901 | C | T | 1 | a0001c0001t0001g0282 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1354+1373C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 11/11 | chr19 | 45035901 | |||||||
| chr19:45035975 | G | A | 1 | a0001c0001t0001g0365 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1355-1430G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 11/11 | chr19 | 45035975 | |||||||
| chr19:45036384 | C | T | 1 | a0001c0001t0001g0079 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1355-1021C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 11/11 | chr19 | 45036384 | |||||||
| chr19:45036578 | T | C | 4 | a0001c0002t0001g0104 a0001c0002t0001g0131 a0001c0002t0001g0133 others(1): Show |
4 | HG02109.hp2 HG02451.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1355-827T>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 11/11 | chr19 | 45036578 | |||||||
| chr19:45036607 | A | G | 1 | a0001c0001t0001g0237 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1355-798A>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 11/11 | chr19 | 45036607 | |||||||
| chr19:45036726 | G | A | 1 | a0001c0001t0004g0201 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1355-679G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 11/11 | chr19 | 45036726 | |||||||
| chr19:45036778 | A | G | 1 | a0001c0001t0001g0130 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1355-627A>G | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 11/11 | chr19 | 45036778 | |||||||
| chr19:45036879 | C | T | 1 | a0001c0001t0001g0368 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1355-526C>T | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 11/11 | chr19 | 45036879 | |||||||
| chr19:45036917 | G | A | 1 | a0001c0001t0001g0307 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1355-488G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 11/11 | chr19 | 45036917 | |||||||
| chr19:45036955 | T | C | 1 | a0001c0001t0003g0189 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1355-450T>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 11/11 | chr19 | 45036955 | |||||||
| chr19:45037108 | G | A | 4 | a0001c0002t0001g0104 a0001c0002t0001g0131 a0001c0002t0001g0133 others(1): Show |
4 | HG02109.hp2 HG02451.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1355-297G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 11/11 | chr19 | 45037108 | |||||||
| chr19:45037149 | G | A | 1 | a0001c0001t0001g0119 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1355-256G>A | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 11/11 | chr19 | 45037149 | |||||||
| chr19:45037182 | G | C | 2 | a0001c0001t0001g0146 a0001c0001t0001g0321 |
2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1355-223G>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 11/11 | chr19 | 45037182 | |||||||
| chr19:45037243 | T | C | 1 | a0001c0001t0001g0370 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1355-162T>C | RELB | ENSG00000104856.15 | transcript | ENST00000221452.13 | protein_coding | 11/11 | chr19 | 45037243 |