Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:192818527..192820522-chr1:192821940..192823525,2	K562	blood:

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs10489514	1.00[ASN][1000 genomes]
rs10921281	0.94[EUR][1000 genomes]
rs12076933	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12087043	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12091901	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1231819	1.00[ASN][1000 genomes]
rs1625786	1.00[ASN][1000 genomes]
rs16834887	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16834924	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16834941	1.00[EUR][1000 genomes]
rs16834945	0.88[EUR][1000 genomes]
rs1770915	1.00[CHD][hapmap];1.00[ASN][1000 genomes]
rs1770918	1.00[ASN][1000 genomes]
rs1775687	1.00[CHD][hapmap];1.00[ASN][1000 genomes]
rs1775688	1.00[ASN][1000 genomes]
rs1775689	1.00[ASN][1000 genomes]
rs1775690	1.00[ASN][1000 genomes]
rs1775691	1.00[ASN][1000 genomes]
rs1775693	1.00[ASN][1000 genomes]
rs2153083	1.00[ASN][1000 genomes]
rs60641679	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61394494	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6660343	1.00[CEU][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6661981	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6700848	1.00[EUR][1000 genomes]
rs715422	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7514204	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7523033	1.00[CHD][hapmap];0.87[TSI][hapmap];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7530747	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7542329	0.94[EUR][1000 genomes];1.00[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	nsv532618	chr1:192537006-193149179	Weak transcription Strong transcription Active TSS Flanking Active TSS Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	70 gene(s)	inside rSNPs	diseases
2	nsv548660	chr1:192609268-192945348	Enhancers Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA	22 gene(s)	inside rSNPs	diseases
3	esv3386987	chr1:192819539-192821168	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:192817000-192819800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
2	chr1:192817600-192821200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
3	chr1:192819200-192820600	Enhancers	Primary neutrophils fromperipheralblood	blood
4	chr1:192819200-192821400	Enhancers	iPS-15b Cell Line	embryonic stem cell

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