Variant report

Variant	rs148139959
Chromosome Location	chr4:46372925-46372926
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 1 )
Associated
traits (count: 0)

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	nsv1007038	chr4:46343910-46413230	Bivalent/Poised TSS Enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Genic enhancers ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:46356400-46386000	Weak transcription	Brain Inferior Temporal Lobe	brain
2	chr4:46366800-46374200	Weak transcription	Brain Anterior Caudate	brain
3	chr4:46366800-46381000	Weak transcription	Brain Angular Gyrus	brain
4	chr4:46369600-46374000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
5	chr4:46370400-46387800	Weak transcription	Fetal Brain Female	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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