Variant report

Variant	rs7304940
Chromosome Location	chr12:21464606-21464607
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 8 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs11045956	0.81[AFR][1000 genomes]
rs11045960	0.81[AFR][1000 genomes]
rs11568573	1.00[AFR][1000 genomes]
rs34211424	0.81[AFR][1000 genomes]
rs7137014	1.00[AFR][1000 genomes]
rs7305484	0.93[AFR][1000 genomes]
rs7952736	1.00[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:1 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv557735	chr12:21443282-21538957	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:21416200-21473600	Weak transcription	Brain Inferior Temporal Lobe	brain
2	chr12:21461000-21467000	Weak transcription	Brain Anterior Caudate	brain
3	chr12:21461000-21473800	Weak transcription	Brain Angular Gyrus	brain
4	chr12:21463600-21466000	Weak transcription	Brain Substantia Nigra	brain
5	chr12:21463800-21468000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
6	chr12:21464400-21464800	Strong transcription	Brain Hippocampus Middle	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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