Variant report

Variant	rs543062693
Chromosome Location	chr7:86268062-86268063
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 2 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1025032	chr7:86032479-86642973	Weak transcription Enhancers Strong transcription Bivalent/Poised TSS Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
2	esv3449095	chr7:86268006-86268525	Weak transcription Enhancers	TF binding region	1 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	chr7:86263800-86268600	Weak transcription	Brain Substantia Nigra	brain
2	chr7:86263800-86268800	Weak transcription	Brain Anterior Caudate	brain
3	chr7:86263800-86268800	Weak transcription	Brain Cingulate Gyrus	brain
4	chr7:86267000-86272600	Weak transcription	Brain Inferior Temporal Lobe	brain
5	chr7:86267400-86269400	Enhancers	Brain Hippocampus Middle	brain
6	chr7:86268000-86271600	Weak transcription	Brain Angular Gyrus	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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