Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:16304365..16307291-chr11:16625396..16627357,2	K562	blood:

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs10832589	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10832590	0.94[ASN][1000 genomes]
rs11023899	0.83[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12225830	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs169859	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1807154	0.94[ASN][1000 genomes]
rs2938282	0.87[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs297320	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs297343	0.94[ASN][1000 genomes]
rs297346	0.94[ASN][1000 genomes]
rs297347	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs297348	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs297351	0.94[ASN][1000 genomes]
rs297352	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs297354	0.94[ASN][1000 genomes]
rs297355	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs297356	0.94[ASN][1000 genomes]
rs297357	0.94[ASN][1000 genomes]
rs297358	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs297360	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs297361	0.94[ASN][1000 genomes]
rs297364	0.94[ASN][1000 genomes]
rs297367	0.94[ASN][1000 genomes]
rs581210	0.89[AMR][1000 genomes];0.83[EUR][1000 genomes];0.82[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv529731	chr11:16122782-16468170	Enhancers Active TSS Bivalent Enhancer Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv897013	chr11:16206658-16307700	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	nsv553565	chr11:16220289-16307700	Enhancers ZNF genes & repeats Active TSS Weak transcription Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	nsv897015	chr11:16235962-16307700	Active TSS Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	esv3335445	chr11:16301976-16306474	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:16286800-16314800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr11:16300200-16313400	Weak transcription	Brain Germinal Matrix	brain
3	chr11:16300800-16314200	Weak transcription	Cortex derived primary cultured neurospheres	brain
4	chr11:16302200-16309000	Weak transcription	Fetal Intestine Small	intestine
5	chr11:16302200-16314200	Weak transcription	Fetal Muscle Leg	muscle
6	chr11:16302200-16321600	Weak transcription	Left Ventricle	heart
7	chr11:16302400-16307600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr11:16302400-16309200	Weak transcription	Fetal Intestine Large	intestine
9	chr11:16303000-16310800	Weak transcription	K562	blood
10	chr11:16305800-16308600	Weak transcription	Pancreatic Islets	Pancreatic Islet

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