Variant report

Variant	rs4695759
Chromosome Location	chr4:174963224-174963225
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 7 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs11133027	0.82[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs4695760	0.90[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs4695761	0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv830155	chr4:174943809-175136483	Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
2	nsv1016910	chr4:174952788-175349057	Bivalent Enhancer Flanking Active TSS Active TSS Enhancers Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
3	nsv537363	chr4:174952788-175349057	Active TSS Bivalent Enhancer Weak transcription Enhancers Strong transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
4	nsv508335	chr4:174961722-174995092	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	n/a

No data

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:174960200-174968600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr4:174960400-174964000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr4:174961200-174964200	Enhancers	iPS-18 Cell Line	embryonic stem cell
4	chr4:174961400-174964200	Enhancers	HUES64 Cell Line	embryonic stem cell
5	chr4:174961400-174964800	Enhancers	iPS-15b Cell Line	embryonic stem cell
6	chr4:174961600-174963400	Enhancers	ES-I3 Cell Line	embryonic stem cell
7	chr4:174961600-174963400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
8	chr4:174961800-174963400	Enhancers	H9 Cell Line	embryonic stem cell
9	chr4:174961800-174964200	Enhancers	H1 Cell Line	embryonic stem cell
10	chr4:174962400-174963400	Enhancers	Fetal Heart	heart
11	chr4:174963000-174963400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr4:174963000-174963400	Enhancers	Colon Smooth Muscle	Colon
13	chr4:174963200-174963400	Active TSS	iPS-20b Cell Line	embryonic stem cell
14	chr4:174963200-174964600	Enhancers	HUES48 Cell Line	embryonic stem cell

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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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