Variant report

Variant	rs73303921
Chromosome Location	chr8:91485001-91485002
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

No data

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:91471834..91475082-chr8:91482886..91485464,3	MCF-7	breast:
2	chr8:91011783..91015230-chr8:91481939..91486676,8	MCF-7	breast:
3	chr17:57934504..57936830-chr8:91484715..91486603,2	MCF-7	breast:
4	chr8:91093569..91094200-chr8:91484781..91485542,2	MCF-7	breast:
5	chr8:91012701..91013726-chr8:91484387..91485651,9	MCF-7	breast:
6	chr8:91264191..91264864-chr8:91484737..91485456,2	MCF-7	breast:
7	chr8:91012746..91013704-chr8:91484534..91485505,7	MCF-7	breast:
8	chr8:90996588..90997373-chr8:91484695..91485656,2	MCF-7	breast:
9	chr8:91484322..91486469-chr8:91486564..91488388,2	MCF-7	breast:

No data

No data

No data

Extended variants
information (count: 23 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs57350729	0.90[AFR][1000 genomes]
rs57550344	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57820529	1.00[AMR][1000 genomes]
rs57982498	1.00[AMR][1000 genomes]
rs57995155	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59588987	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61305476	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61504138	0.90[AFR][1000 genomes]
rs73303917	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73303924	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73303926	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73303930	0.97[AFR][1000 genomes]
rs73303944	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73303958	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73303965	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73303968	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73303972	1.00[AMR][1000 genomes]
rs73303973	1.00[AMR][1000 genomes]
rs73303974	1.00[AMR][1000 genomes]
rs73303980	1.00[AMR][1000 genomes]
rs73303981	1.00[AMR][1000 genomes]
rs73303984	1.00[AMR][1000 genomes]
rs73303987	1.00[AMR][1000 genomes]

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:91480600-91491200	Weak transcription	Liver	Liver
2	chr8:91483600-91485200	Enhancers	HMEC	breast
3	chr8:91483600-91485600	Enhancers	NHDF-Ad	bronchial
4	chr8:91483600-91485800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr8:91484000-91485200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr8:91484800-91485200	Enhancers	K562	blood
7	chr8:91484800-91485600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr8:91485000-91485200	Enhancers	Pancreatic Islets	Pancreatic Islet

Quick Search:

Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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