Variant report

Variant	rs28608760
Chromosome Location	chr4:22194320-22194321
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 20 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs10000922	0.85[AFR][1000 genomes]
rs10000930	0.85[AFR][1000 genomes]
rs10003031	0.95[AFR][1000 genomes]
rs10006914	0.95[AFR][1000 genomes]
rs10011522	0.86[AFR][1000 genomes]
rs10012709	0.85[AFR][1000 genomes]
rs10015098	0.95[AFR][1000 genomes]
rs10017962	0.85[AFR][1000 genomes]
rs10026514	0.95[AFR][1000 genomes]
rs1080513	0.95[AFR][1000 genomes]
rs6852409	0.85[AFR][1000 genomes]
rs6852761	0.85[AFR][1000 genomes]
rs9291438	0.85[AFR][1000 genomes]
rs9291439	0.85[AFR][1000 genomes]
rs9990539	0.95[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv817467	chr4:21602921-22422816	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	esv2757925	chr4:22011581-22230718	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	esv2759232	chr4:22011581-22230718	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	nsv829881	chr4:22084704-22254679	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	nsv593822	chr4:22165174-22246276	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:22192000-22194800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr4:22192200-22194400	Enhancers	ES-I3 Cell Line	embryonic stem cell
3	chr4:22192200-22194600	Enhancers	HUES64 Cell Line	embryonic stem cell
4	chr4:22192200-22194800	Enhancers	HUES48 Cell Line	embryonic stem cell
5	chr4:22192600-22194800	Enhancers	HUES6 Cell Line	embryonic stem cell
6	chr4:22192800-22194800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr4:22193000-22194400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr4:22193200-22194400	Weak transcription	NHEK	skin
9	chr4:22193200-22194800	Enhancers	iPS-15b Cell Line	embryonic stem cell
10	chr4:22193200-22194800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
11	chr4:22193400-22194800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr4:22193800-22194400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr4:22194000-22194800	Enhancers	iPS-18 Cell Line	embryonic stem cell
14	chr4:22194200-22194800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr4:22194200-22198000	Weak transcription	Adipose Nuclei	Adipose

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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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