Variant report

Variant	rs11068453
Chromosome Location	chr12:117785047-117785048
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 9 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs11068454	0.96[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11609784	0.98[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11613900	0.98[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12811414	0.81[ASN][1000 genomes]
rs17431015	0.81[ASN][1000 genomes]
rs17509231	0.98[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs3782222	0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs3814246	0.87[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs939473	0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:117771600-117789000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr12:117777200-117785400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr12:117777400-117785400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr12:117782800-117796400	Weak transcription	Skeletal Muscle Female	skeletal muscle
5	chr12:117783000-117788200	Weak transcription	Skeletal Muscle Male	skeletal muscle
6	chr12:117784600-117785200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr12:117784600-117786200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr12:117785000-117785600	Enhancers	NHEK	skin

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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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