Variant report

Variant	rs7142452
Chromosome Location	chr14:84805020-84805021
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr14:84796952..84798604-chr14:84802192..84805102,2	K562	blood:

Extended variants
information (count: 30 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs4411445	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61983313	0.88[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs61983315	0.82[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs61983320	0.88[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs61983323	0.94[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs61984186	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61984209	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61984241	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61984242	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61984243	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61984248	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61984249	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61984250	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61984252	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61984753	1.00[ASN][1000 genomes]
rs61985587	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61985589	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61985590	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61985591	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61985592	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61985593	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61985594	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61985599	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61985601	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61985645	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61985646	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7154659	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7155005	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8010754	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv832845	chr14:84726378-84900199	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	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	chr14:84804800-84807000	Weak transcription	HUVEC	blood vessel

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