Variant report

Variant	rs34084814
Chromosome Location	chr12:118278681-118278682
allele	C/T
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]
rs10850907	1.00[AMR][1000 genomes];0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10850908	0.89[ASN][1000 genomes]
rs11068695	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2393327	0.92[ASN][1000 genomes]
rs4328289	0.95[ASN][1000 genomes]
rs4516059	0.86[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs56111943	0.88[EUR][1000 genomes]
rs56322070	0.80[ASN][1000 genomes]
rs56370061	1.00[AMR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs59114295	0.81[EUR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:118275200-118281800	Weak transcription	Brain Anterior Caudate	brain
2	chr12:118275600-118280800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
3	chr12:118275600-118281000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
4	chr12:118275800-118280000	Weak transcription	H1 Cell Line	embryonic stem cell
5	chr12:118275800-118280600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
6	chr12:118277600-118279000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr12:118277800-118281000	Weak transcription	H9 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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