Variant report

Variant	rs41264463
Chromosome Location	chr1:159110372-159110373
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 10 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs11580888	0.92[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs11582615	0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11586482	0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs28620204	0.92[ASN][1000 genomes]
rs3026921	0.96[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs3026922	0.96[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs3026925	0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3026935	0.91[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs61400225	0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs863039	0.95[ASN][1000 genomes]

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:159109400-159110600	Enhancers	Fetal Brain Male	brain
2	chr1:159110200-159110400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr1:159110200-159110400	Enhancers	Brain Germinal Matrix	brain
4	chr1:159110200-159110600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
5	chr1:159110200-159111600	Enhancers	H1 Cell Line	embryonic stem cell
6	chr1:159110200-159113400	Active TSS	Fetal Brain Female	brain

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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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