Variant report

Variant	rs6819060
Chromosome Location	chr4:130250283-130250284
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr4:130243320..130247146-chr4:130247624..130250769,3	K562	blood:

Extended variants
information (count: 29 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs10018742	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs11939768	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs11939883	0.90[EUR][1000 genomes]
rs28459462	0.87[ASN][1000 genomes]
rs4246723	0.94[AFR][1000 genomes];0.89[AMR][1000 genomes];0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4246725	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs4324562	0.85[ASN][1000 genomes]
rs4348109	0.87[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs4351033	0.94[AFR][1000 genomes];0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4356920	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs4364276	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4525996	0.84[ASN][1000 genomes]
rs4604071	0.94[AFR][1000 genomes];0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4608824	0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4975217	0.90[EUR][1000 genomes]
rs5019103	0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs5019104	0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs62317265	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs6534725	0.91[AFR][1000 genomes];0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6534727	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs6814634	0.91[AFR][1000 genomes];0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6818545	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs6821513	0.87[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs6842148	0.93[AFR][1000 genomes];0.89[AMR][1000 genomes];0.89[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7656960	0.91[AFR][1000 genomes];0.89[AMR][1000 genomes];0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs9994470	0.87[AFR][1000 genomes];0.86[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	nsv534538	chr4:129799138-130431688	Enhancers Weak transcription Strong transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
2	nsv830058	chr4:130136025-130315471	Weak transcription Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	nsv879932	chr4:130167642-130264517	Weak transcription Flanking Active TSS Enhancers Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:130246000-130251000	Enhancers	Primary monocytes fromperipheralblood	blood
2	chr4:130249800-130256000	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr4:130250200-130251000	Enhancers	Monocytes-CD14+_RO01746	blood

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