Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:60303688..60306205-chr8:60408820..60411087,2	K562	blood:

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs10107018	0.82[AMR][1000 genomes]
rs10957091	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11987803	0.82[AMR][1000 genomes]
rs11995865	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12544847	0.82[AMR][1000 genomes]
rs12548205	0.82[AMR][1000 genomes]
rs13282650	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1401425	0.82[AMR][1000 genomes]
rs2139235	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2326323	0.82[AMR][1000 genomes]
rs3942395	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4316141	0.82[AFR][1000 genomes];0.96[AMR][1000 genomes];0.85[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6471785	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6981902	0.82[AMR][1000 genomes]
rs6997718	0.82[AMR][1000 genomes]
rs7005684	0.82[AMR][1000 genomes]
rs7006092	0.82[AMR][1000 genomes]
rs7006236	0.82[AMR][1000 genomes]
rs7820669	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs7830834	0.94[AFR][1000 genomes];0.96[AMR][1000 genomes];0.85[EUR][1000 genomes];0.91[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1029441	chr8:60099776-60539141	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv539629	chr8:60099776-60539141	ZNF genes & repeats Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv831329	chr8:60162977-60356031	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
4	nsv831330	chr8:60270398-60514078	Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:60302000-60305800	Enhancers	Fetal Intestine Large	intestine
2	chr8:60302200-60305800	Enhancers	Fetal Intestine Small	intestine
3	chr8:60304000-60305400	Enhancers	Fetal Heart	heart
4	chr8:60304000-60307400	Weak transcription	Osteobl	bone
5	chr8:60304200-60305400	Enhancers	Duodenum Mucosa	Duodenum
6	chr8:60304400-60305800	Enhancers	Rectal Mucosa Donor 31	rectum
7	chr8:60304600-60305400	Enhancers	Small Intestine	intestine
8	chr8:60304800-60305800	Enhancers	Stomach Mucosa	stomach
9	chr8:60305200-60305400	Enhancers	Colonic Mucosa	Colon
10	chr8:60305200-60305400	Enhancers	Rectal Mucosa Donor 29	rectum
11	chr8:60305200-60305600	Enhancers	Sigmoid Colon	Sigmoid Colon
12	chr8:60305200-60306000	Enhancers	Dnd41	blood

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