Variant report

Variant	rs4305728
Chromosome Location	chr6:16890561-16890562
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs12202769	0.87[ASN][1000 genomes]
rs4311514	0.93[ASN][1000 genomes]
rs55678019	0.80[ASN][1000 genomes]
rs62390565	0.94[ASN][1000 genomes]
rs770938	0.81[ASN][1000 genomes]
rs9464959	0.94[ASN][1000 genomes]
rs9477241	0.82[ASN][1000 genomes]
rs9477244	0.94[ASN][1000 genomes]
rs9477248	0.90[ASN][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	esv2758037	chr6:16873271-16912538	Flanking Active TSS Weak transcription Enhancers Active TSS ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
2	esv2759409	chr6:16873271-16912538	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
3	nsv601016	chr6:16885017-16892412	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:16886400-16891200	Weak transcription	K562	blood
2	chr6:16886600-16890600	Active TSS	HUES6 Cell Line	embryonic stem cell
3	chr6:16888600-16890600	Enhancers	Primary monocytes fromperipheralblood	blood
4	chr6:16889800-16890600	Enhancers	Monocytes-CD14+_RO01746	blood
5	chr6:16890400-16890600	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
6	chr6:16890400-16890600	Active TSS	H9 Cell Line	embryonic stem cell
7	chr6:16890400-16890600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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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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