Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:168089396..168091403-chr2:168092947..168095096,2	K562	blood:

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

rs_ID	r²[population]
rs10497323	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12611980	0.95[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12612028	0.95[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs16853244	1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1842233	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2204279	0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4315485	0.81[ASN][1000 genomes]
rs4610018	0.92[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs57543537	1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs60477253	0.80[EUR][1000 genomes]
rs6432989	1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6708386	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6746061	1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs73029721	0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7419512	1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7556840	1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7560985	0.81[ASN][1000 genomes]
rs7564986	0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7569158	1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7602065	0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7602119	1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7603500	0.83[EUR][1000 genomes]
rs7605309	0.80[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs9784125	0.83[EUR][1000 genomes];0.81[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	nsv583591	chr2:168037489-168132892	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region miRNA target site	2 gene(s)	inside rSNPs	diseases
2	nsv875377	chr2:168084857-168203116	Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	2 gene(s)	inside rSNPs	diseases
3	nsv979347	chr2:168092753-168141678	Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers	Chromatin interactive region miRNA target site	n/a	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:168056800-168114000	Weak transcription	Psoas Muscle	Psoas
2	chr2:168067400-168096000	Weak transcription	Left Ventricle	heart
3	chr2:168083800-168095800	Weak transcription	Skeletal Muscle Male	skeletal muscle
4	chr2:168085000-168098600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr2:168085200-168097000	Weak transcription	Skeletal Muscle Female	skeletal muscle

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