Variant report

Variant	rs12202381
Chromosome Location	chr6:24139942-24139943
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 4 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:3)

rs_ID	r²[population]
rs12190701	1.00[CHB][hapmap]
rs12196541	0.82[GIH][hapmap]
rs9358755	1.00[CHB][hapmap]

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	nsv1029930	chr6:23481989-24289948	Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Weak transcription Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs12202381	DCDC2	cis	parietal	SCAN

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:24127200-24141000	Weak transcription	Brain Cingulate Gyrus	brain
2	chr6:24127600-24140600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
3	chr6:24127600-24146800	Weak transcription	Pancreatic Islets	Pancreatic Islet
4	chr6:24127800-24140600	Weak transcription	Brain Anterior Caudate	brain
5	chr6:24127800-24140600	Weak transcription	Brain Inferior Temporal Lobe	brain
6	chr6:24128600-24140600	Weak transcription	Fetal Brain Male	brain
7	chr6:24129400-24140000	Weak transcription	Brain Germinal Matrix	brain
8	chr6:24135400-24140600	Weak transcription	Brain Angular Gyrus	brain
9	chr6:24139800-24140600	Strong transcription	Fetal Brain Female	brain
10	chr6:24139800-24140600	Enhancers	HepG2	liver

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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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