Variant report

Variant	rs6840833
Chromosome Location	chr4:74629065-74629066
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 22 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs10033377	1.00[EUR][1000 genomes]
rs16849925	1.00[EUR][1000 genomes]
rs1951237	1.00[EUR][1000 genomes]
rs2227525	1.00[EUR][1000 genomes]
rs2227532	1.00[EUR][1000 genomes]
rs2227545	1.00[EUR][1000 genomes]
rs28544060	1.00[EUR][1000 genomes]
rs28560265	1.00[EUR][1000 genomes]
rs28707294	1.00[EUR][1000 genomes]
rs28879705	1.00[EUR][1000 genomes]
rs55648028	1.00[EUR][1000 genomes]
rs59569175	1.00[EUR][1000 genomes]
rs6847987	1.00[EUR][1000 genomes]
rs6853880	1.00[EUR][1000 genomes]
rs73827899	1.00[EUR][1000 genomes]
rs73827900	1.00[EUR][1000 genomes]
rs7657469	1.00[EUR][1000 genomes]
rs7668660	1.00[EUR][1000 genomes]
rs7673632	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1001725	chr4:74354050-74860924	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
2	nsv530126	chr4:74376622-74843892	Bivalent Enhancer Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Active TSS Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
3	nsv1005231	chr4:74555497-74680079	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:74625200-74629400	Enhancers	Primary monocytes fromperipheralblood	blood
2	chr4:74627600-74629200	Enhancers	Primary hematopoietic stem cells short term culture	blood
3	chr4:74628600-74629600	Enhancers	Primary neutrophils fromperipheralblood	blood
4	chr4:74628600-74629600	Enhancers	Monocytes-CD14+_RO01746	blood
5	chr4:74629000-74629800	Enhancers	Lung	lung

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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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