Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr3:177709402..177711641-chr3:177711937..177714399,2	K562	blood:
2	chr3:177076309..177079025-chr3:177709045..177711034,2	K562	blood:

rSNPs within LD-proxies of this variant (count:37)

rs_ID	r²[population]
rs1075544	0.88[ASN][1000 genomes]
rs10936960	0.88[ASN][1000 genomes]
rs11919677	0.83[ASN][1000 genomes]
rs11922170	0.85[ASN][1000 genomes]
rs12495203	0.96[ASN][1000 genomes]
rs13066104	0.88[ASN][1000 genomes]
rs13087011	0.87[ASN][1000 genomes]
rs13314585	0.87[ASN][1000 genomes]
rs1362829	0.91[ASN][1000 genomes]
rs1421157	0.88[ASN][1000 genomes]
rs1421158	0.88[ASN][1000 genomes]
rs1421160	0.88[ASN][1000 genomes]
rs1421161	0.88[ASN][1000 genomes]
rs1421162	0.88[ASN][1000 genomes]
rs1421166	0.91[ASN][1000 genomes]
rs1421167	0.91[ASN][1000 genomes]
rs1421173	0.88[ASN][1000 genomes]
rs1895068	0.88[ASN][1000 genomes]
rs1895072	0.86[AMR][1000 genomes];0.86[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2160836	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs3961634	0.81[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs57315928	0.88[ASN][1000 genomes]
rs6769109	0.88[ASN][1000 genomes]
rs6775970	0.91[ASN][1000 genomes]
rs6776256	0.96[ASN][1000 genomes]
rs6783796	0.91[ASN][1000 genomes]
rs6786110	0.83[ASN][1000 genomes]
rs6804905	0.88[ASN][1000 genomes]
rs6807952	0.91[ASN][1000 genomes]
rs6808901	0.85[ASN][1000 genomes]
rs737553	0.88[ASN][1000 genomes]
rs737555	0.87[ASN][1000 genomes]
rs7645977	0.89[ASN][1000 genomes]
rs9830203	0.91[ASN][1000 genomes]
rs9838142	0.88[ASN][1000 genomes]
rs9862300	0.88[ASN][1000 genomes]
rs9875424	0.88[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	nsv931055	chr3:177229521-177889872	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
2	nsv829805	chr3:177662113-177805003	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv997975	chr3:177664921-177719623	Enhancers Flanking Active TSS Weak transcription Active TSS	TF binding region CpG island Chromatin interactive region	2 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	chr3:177710000-177711800	Enhancers	Fetal Intestine Large	intestine
2	chr3:177710200-177711600	Enhancers	Fetal Intestine Small	intestine
3	chr3:177710200-177711600	Enhancers	HepG2	liver

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