Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:165420099..165422581-chr1:165428769..165430310,2	K562	blood:

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs10800099	0.88[ASN][1000 genomes]
rs10918182	0.83[ASN][1000 genomes]
rs10918183	0.83[ASN][1000 genomes]
rs10918184	0.88[ASN][1000 genomes]
rs10918185	0.88[ASN][1000 genomes]
rs10918186	0.86[ASN][1000 genomes]
rs10918189	0.88[ASN][1000 genomes]
rs10918190	0.88[ASN][1000 genomes]
rs10918191	0.88[ASN][1000 genomes]
rs10918192	0.80[ASN][1000 genomes]
rs10918193	0.89[ASN][1000 genomes]
rs12086907	0.90[ASN][1000 genomes]
rs12088020	0.89[ASN][1000 genomes]
rs12091454	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12561930	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12566694	0.88[ASN][1000 genomes]
rs16844905	0.83[ASN][1000 genomes]
rs16844913	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4656446	0.83[ASN][1000 genomes]
rs4656447	0.88[ASN][1000 genomes]
rs4657439	0.88[ASN][1000 genomes]
rs6699656	0.80[ASN][1000 genomes]
rs7542419	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	esv2756868	chr1:165417526-165425536	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
2	esv2758974	chr1:165417526-165425536	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	nsv8524	chr1:165421277-165424974	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:165415400-165422000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr1:165420400-165424400	Enhancers	Fetal Muscle Leg	muscle
3	chr1:165421000-165421600	Enhancers	Fetal Heart	heart
4	chr1:165421000-165422400	Enhancers	Psoas Muscle	Psoas
5	chr1:165421000-165422400	Enhancers	Skeletal Muscle Female	skeletal muscle
6	chr1:165421200-165422000	Weak transcription	Left Ventricle	heart

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