Variant report

No.	Distal block	Cell Line	Cell type
1	chr1:184207341..184210185-chr1:184231438..184233613,2	K562	blood:
2	chr1:184208506..184210470-chr1:184213675..184215475,2	K562	blood:
3	chr1:184208506..184210227-chr1:184212318..184215475,3	K562	blood:

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs10494579	0.88[ASN][1000 genomes]
rs1111087	0.88[ASN][1000 genomes]
rs13375618	0.88[ASN][1000 genomes]
rs13375785	0.88[ASN][1000 genomes]
rs16822649	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs16822650	0.89[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs16822722	0.88[ASN][1000 genomes]
rs16822757	0.88[ASN][1000 genomes]
rs16822764	0.88[ASN][1000 genomes]
rs16822783	0.88[ASN][1000 genomes]
rs16822793	0.88[ASN][1000 genomes]
rs1810915	0.88[ASN][1000 genomes]
rs1930289	0.88[ASN][1000 genomes]
rs2161987	0.88[ASN][1000 genomes]
rs4354502	0.88[ASN][1000 genomes]
rs4543760	0.88[ASN][1000 genomes]
rs56797986	0.88[ASN][1000 genomes]
rs59737381	0.88[ASN][1000 genomes]
rs59786945	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs59949779	0.88[ASN][1000 genomes]
rs6656900	0.83[ASN][1000 genomes]
rs73057576	0.89[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs73057582	0.88[AFR][1000 genomes];0.87[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs73057595	0.88[ASN][1000 genomes]
rs73057598	0.88[ASN][1000 genomes]
rs73059524	0.88[ASN][1000 genomes]
rs73059529	0.88[ASN][1000 genomes]
rs73059544	0.88[ASN][1000 genomes]
rs7543951	0.88[ASN][1000 genomes]
rs7552391	0.83[ASN][1000 genomes]
rs755483	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.88[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	nsv530079	chr1:183797938-184639971	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:184197200-184209200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr1:184207000-184211800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr1:184209200-184209400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived

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