Variant report

Variant	rs73227938
Chromosome Location	chr3:135174671-135174672
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 3 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs824099	0.83[ASN][1000 genomes]

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	nsv460860	chr3:135107678-135769006	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Strong transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
2	nsv591829	chr3:135107678-135769006	Flanking Active TSS Strong transcription Active TSS Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:135171800-135174800	Weak transcription	HUES64 Cell Line	embryonic stem cell
2	chr3:135172400-135175000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr3:135174400-135175200	Enhancers	iPS-15b Cell Line	embryonic stem cell
4	chr3:135174400-135175200	Enhancers	iPS-18 Cell Line	embryonic stem cell
5	chr3:135174400-135175400	Enhancers	H1 Cell Line	embryonic stem cell
6	chr3:135174600-135174800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
7	chr3:135174600-135174800	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
8	chr3:135174600-135175200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
9	chr3:135174600-135175400	Enhancers	Brain Germinal Matrix	brain
10	chr3:135174600-135175600	Enhancers	Fetal Brain Male	brain
11	chr3:135174600-135178600	Weak transcription	Spleen	Spleen

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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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