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]
rs10093286	0.97[ASN][1000 genomes]
rs10102694	0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10102793	0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10103006	0.97[ASN][1000 genomes]
rs10106890	0.97[ASN][1000 genomes]
rs1467228	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs16924885	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16924887	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16924893	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2139233	0.94[ASN][1000 genomes]
rs28574270	0.97[ASN][1000 genomes]
rs28651207	0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs28672242	0.97[ASN][1000 genomes]
rs6471787	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6992861	0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7011055	0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7011263	0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7011488	0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7830772	0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7835053	0.92[EUR][1000 genomes];0.98[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:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:60301600-60305200	Weak transcription	Dnd41	blood
2	chr8:60302000-60305800	Enhancers	Fetal Intestine Large	intestine
3	chr8:60302200-60304600	Enhancers	NHDF-Ad	bronchial
4	chr8:60302200-60305800	Enhancers	Fetal Intestine Small	intestine
5	chr8:60302600-60304400	Enhancers	Stomach Mucosa	stomach
6	chr8:60303400-60304600	Weak transcription	Small Intestine	intestine
7	chr8:60303400-60305200	Weak transcription	Colonic Mucosa	Colon
8	chr8:60303400-60305200	Weak transcription	Sigmoid Colon	Sigmoid Colon
9	chr8:60304000-60304400	Active TSS	Rectal Mucosa Donor 29	rectum
10	chr8:60304000-60304400	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
11	chr8:60304000-60305400	Enhancers	Fetal Heart	heart
12	chr8:60304000-60307400	Weak transcription	Osteobl	bone
13	chr8:60304200-60305000	Enhancers	Fetal Lung	lung
14	chr8:60304200-60305400	Enhancers	Duodenum Mucosa	Duodenum

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