Variant report

Variant	rs2391326
Chromosome Location	chr4:129652971-129652972
allele	C/G
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]
rs2391327	0.82[EUR][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	nsv869258	chr4:129191619-130138148	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	79 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:129633000-129689600	Weak transcription	Right Atrium	heart
2	chr4:129647000-129653400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr4:129647000-129653600	Weak transcription	H1 Cell Line	embryonic stem cell
4	chr4:129647000-129658200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
5	chr4:129647400-129653600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
6	chr4:129647400-129654600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
7	chr4:129649400-129653400	Weak transcription	HUES48 Cell Line	embryonic stem cell
8	chr4:129649400-129653600	Weak transcription	HUES64 Cell Line	embryonic stem cell
9	chr4:129649400-129653800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
10	chr4:129649400-129658000	Weak transcription	Fetal Heart	heart

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dbSNP/dbVar ID: rs12345 /nsv7879
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