Variant report

Variant	rs12512066
Chromosome Location	chr4:152711435-152711436
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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

rSNPs within LD-proxies of this variant (count:1)

rs_ID	r²[population]
rs3762907	1.00[ASN][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	nsv432644	chr4:152635395-153023402	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Strong transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:152708000-152717600	Weak transcription	Fetal Intestine Small	intestine
2	chr4:152709000-152712600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr4:152710600-152714400	Enhancers	Fetal Heart	heart
4	chr4:152710800-152712400	Weak transcription	HUES64 Cell Line	embryonic stem cell
5	chr4:152710800-152712800	Enhancers	Ovary	ovary
6	chr4:152711000-152711800	Weak transcription	HUES48 Cell Line	embryonic stem cell
7	chr4:152711000-152712000	Weak transcription	HUES6 Cell Line	embryonic stem cell
8	chr4:152711000-152720000	Weak transcription	H9 Cell Line	embryonic stem cell
9	chr4:152711200-152712400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell

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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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