Variant report

Variant	rs73174567
Chromosome Location	chr2:10987581-10987582
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 4 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:4)

rs_ID	r²[population]
rs56930105	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs59164865	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62120278	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6718064	0.85[ASN][1000 genomes]

No data

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:10979400-11000400	Weak transcription	Fetal Brain Male	brain
2	chr2:10984400-10988000	Active TSS	Right Atrium	heart
3	chr2:10984400-10988600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr2:10984800-10988800	Weak transcription	Cortex derived primary cultured neurospheres	brain
5	chr2:10985800-10988000	Enhancers	HepG2	liver
6	chr2:10986000-10988000	Enhancers	Brain Cingulate Gyrus	brain
7	chr2:10986000-10988000	Enhancers	Brain Inferior Temporal Lobe	brain
8	chr2:10986000-10989000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
9	chr2:10986400-10988800	Enhancers	Skeletal Muscle Female	skeletal muscle
10	chr2:10986800-10987600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
11	chr2:10987000-10989200	Enhancers	Skeletal Muscle Male	skeletal muscle
12	chr2:10987200-10988400	Enhancers	Left Ventricle	heart
13	chr2:10987200-10990800	Weak transcription	Psoas Muscle	Psoas
14	chr2:10987400-10988200	Enhancers	Right Ventricle	heart

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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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