Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr14:84493242..84495734-chr14:84508485..84511044,2	K562	blood:

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs11844203	0.88[EUR][1000 genomes]
rs11846485	0.89[EUR][1000 genomes]
rs11847648	0.88[EUR][1000 genomes]
rs11851449	0.88[EUR][1000 genomes]
rs11851578	0.88[EUR][1000 genomes]
rs17119456	0.87[EUR][1000 genomes]
rs17119530	0.91[EUR][1000 genomes]
rs17119545	0.92[EUR][1000 genomes]
rs17119546	0.93[EUR][1000 genomes]
rs17119555	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17657042	0.91[AFR][1000 genomes]
rs17727999	0.90[EUR][1000 genomes]
rs17730419	0.91[AFR][1000 genomes]
rs41407845	0.90[EUR][1000 genomes]
rs4551972	0.82[AFR][1000 genomes]
rs55645564	0.91[AFR][1000 genomes]
rs57196167	0.83[EUR][1000 genomes]
rs60773969	0.92[EUR][1000 genomes]
rs7140245	0.81[EUR][1000 genomes]
rs72701037	0.92[EUR][1000 genomes]
rs72701046	0.92[EUR][1000 genomes]
rs72701082	0.86[AFR][1000 genomes]
rs72701083	0.86[AFR][1000 genomes]
rs72701092	0.82[AFR][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	nsv1382	chr14:84487547-84532237	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs17119553	FLRT2	cis	parietal	SCAN

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:84508200-84510400	Enhancers	Fetal Heart	heart
2	chr14:84508400-84509800	Enhancers	Breast Myoepithelial Primary Cells	Breast
3	chr14:84509000-84510000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr14:84509400-84510000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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