Variant report

Variant	rs12147576
Chromosome Location	chr14:79178150-79178151
allele	C/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]
rs12147836	1.00[CEU][hapmap];1.00[AFR][1000 genomes];0.89[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs17835614	0.88[EUR][1000 genomes]
rs17835635	0.82[CEU][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs56325306	0.89[AFR][1000 genomes];0.88[EUR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:79165000-79181000	Weak transcription	Brain Inferior Temporal Lobe	brain
2	chr14:79176000-79189000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
3	chr14:79176600-79188600	Weak transcription	Brain Anterior Caudate	brain
4	chr14:79177000-79188400	Weak transcription	Brain Angular Gyrus	brain
5	chr14:79177200-79187400	Weak transcription	Brain Germinal Matrix	brain
6	chr14:79177200-79188000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain

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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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