Variant report
Variant | rs7191507 |
---|---|
Chromosome Location | chr16:64844696-64844697 |
allele | A/G |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:1)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
(count:1 , 50 per page) page:
1
No. | Distal block | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr16:64843150..64845918-chr16:64868153..64870678,2 | MCF-7 | breast: |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs1024480 | 1.00[ASN][1000 genomes] |
rs10459802 | 1.00[ASN][1000 genomes] |
rs11075548 | 1.00[ASN][1000 genomes] |
rs121676 | 1.00[ASN][1000 genomes] |
rs142058 | 1.00[ASN][1000 genomes] |
rs1423993 | 1.00[ASN][1000 genomes] |
rs17410049 | 0.85[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs17410111 | 0.85[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs17487617 | 0.82[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs17487665 | 0.82[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs17495513 | 0.93[AFR][1000 genomes];0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs189130 | 1.00[ASN][1000 genomes] |
rs2107371 | 1.00[ASN][1000 genomes] |
rs2107372 | 1.00[ASN][1000 genomes] |
rs2214541 | 1.00[ASN][1000 genomes] |
rs231038 | 1.00[ASN][1000 genomes] |
rs231056 | 1.00[ASN][1000 genomes] |
rs231057 | 1.00[ASN][1000 genomes] |
rs231058 | 1.00[ASN][1000 genomes] |
rs231059 | 1.00[ASN][1000 genomes] |
rs231060 | 1.00[ASN][1000 genomes] |
rs231062 | 1.00[ASN][1000 genomes] |
rs231063 | 1.00[ASN][1000 genomes] |
rs231064 | 1.00[ASN][1000 genomes] |
rs231065 | 1.00[ASN][1000 genomes] |
rs231066 | 1.00[ASN][1000 genomes] |
rs231067 | 1.00[ASN][1000 genomes] |
rs231068 | 1.00[ASN][1000 genomes] |
rs231070 | 1.00[ASN][1000 genomes] |
rs231071 | 1.00[ASN][1000 genomes] |
rs231072 | 1.00[ASN][1000 genomes] |
rs231073 | 1.00[ASN][1000 genomes] |
rs231074 | 1.00[ASN][1000 genomes] |
rs231075 | 1.00[ASN][1000 genomes] |
rs231079 | 1.00[ASN][1000 genomes] |
rs231080 | 1.00[ASN][1000 genomes] |
rs231081 | 1.00[ASN][1000 genomes] |
rs231082 | 1.00[ASN][1000 genomes] |
rs231083 | 1.00[ASN][1000 genomes] |
rs231085 | 1.00[ASN][1000 genomes] |
rs231086 | 1.00[ASN][1000 genomes] |
rs231087 | 1.00[ASN][1000 genomes] |
rs231088 | 1.00[ASN][1000 genomes] |
rs231090 | 1.00[ASN][1000 genomes] |
rs231092 | 1.00[ASN][1000 genomes] |
rs231094 | 1.00[ASN][1000 genomes] |
rs231095 | 1.00[ASN][1000 genomes] |
rs231096 | 1.00[ASN][1000 genomes] |
rs231098 | 1.00[ASN][1000 genomes] |
rs231099 | 1.00[ASN][1000 genomes] |
rs231100 | 1.00[ASN][1000 genomes] |
rs231101 | 1.00[ASN][1000 genomes] |
rs231102 | 1.00[ASN][1000 genomes] |
rs231103 | 1.00[ASN][1000 genomes] |
rs231105 | 1.00[ASN][1000 genomes] |
rs231107 | 1.00[ASN][1000 genomes] |
rs231108 | 1.00[ASN][1000 genomes] |
rs231109 | 1.00[ASN][1000 genomes] |
rs231110 | 1.00[ASN][1000 genomes] |
rs231117 | 0.80[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs231120 | 0.82[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs231122 | 0.84[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs373148 | 1.00[ASN][1000 genomes] |
rs428500 | 1.00[ASN][1000 genomes] |
rs4967865 | 1.00[ASN][1000 genomes] |
rs57941915 | 1.00[ASN][1000 genomes] |
rs62040425 | 0.86[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs62041811 | 0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs62041812 | 0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs62044496 | 0.83[AFR][1000 genomes];0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs62044497 | 0.84[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs62044499 | 0.81[AMR][1000 genomes];0.98[EUR][1000 genomes] |
rs7184774 | 1.00[ASN][1000 genomes] |
rs72788800 | 0.84[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72790807 | 0.81[AMR][1000 genomes];0.98[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv572899 | chr16:64814244-64870659 | Enhancers Weak transcription Bivalent Enhancer | Chromatin interactive region | n/a | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr16:64843200-64847600 | Weak transcription | Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells | embryonic stem cell |