Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:103657443..103659638-chr7:103669864..103671987,2	K562	blood:
2	chr7:103658138..103659805-chr7:103669387..103671987,2	K562	blood:

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs10216187	0.89[ASN][1000 genomes]
rs10216198	0.89[ASN][1000 genomes]
rs10224925	0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10230068	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10273035	0.88[ASN][1000 genomes]
rs10487182	0.85[ASN][1000 genomes]
rs11971265	0.88[ASN][1000 genomes]
rs17158113	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs17158137	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs17158144	0.88[ASN][1000 genomes]
rs17158288	0.90[ASN][1000 genomes]
rs55825925	0.90[ASN][1000 genomes]
rs56272143	0.88[ASN][1000 genomes]
rs60375583	0.90[ASN][1000 genomes]
rs61244293	0.80[EUR][1000 genomes]
rs6465955	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6465957	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs71154387	0.84[ASN][1000 genomes]
rs73409925	0.90[ASN][1000 genomes]
rs73409927	0.88[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv888924	chr7:103637906-103706936	Enhancers Active TSS Weak transcription Genic enhancers Flanking Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv1018253	chr7:103669491-103731850	Enhancers Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:103671800-103672200	Enhancers	Brain Substantia Nigra	brain

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