Variant report

Variant	rs513911
Chromosome Location	chr18:8674524-8674525
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs321650	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs34405335	1.00[EUR][1000 genomes]
rs373423	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs512116	1.00[EUR][1000 genomes]
rs524170	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs524445	1.00[EUR][1000 genomes]
rs527188	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs597151	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs598320	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs627367	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73388260	1.00[EUR][1000 genomes]
rs7342989	1.00[EUR][1000 genomes]

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:8653800-8703400	Weak transcription	Right Atrium	heart
2	chr18:8671800-8674600	Enhancers	HUES48 Cell Line	embryonic stem cell
3	chr18:8672200-8674600	Enhancers	iPS-18 Cell Line	embryonic stem cell
4	chr18:8672600-8674600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr18:8674200-8674600	Enhancers	A549	lung
6	chr18:8674200-8674800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
7	chr18:8674400-8675800	Weak transcription	HUES6 Cell Line	embryonic stem cell

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

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