Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:166722635..166726585-chr6:166755013..166756920,3	K562	blood:
2	chr6:166720530..166722265-chr6:166724559..166726140,2	K562	blood:

Variant related genes	Relation type
ENSG00000176381	Chromatin interaction
ENSG00000198818	Chromatin interaction

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

rs_ID	r²[population]
rs10946157	0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12214433	0.84[ASN][1000 genomes]
rs12214614	0.84[ASN][1000 genomes]
rs13204594	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1998167	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs1998168	0.86[AMR][1000 genomes];0.84[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs3926288	0.82[AMR][1000 genomes]
rs4441936	0.87[AMR][1000 genomes];0.84[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4710037	0.87[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs4710038	0.85[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs4710039	0.85[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs7454264	0.84[ASN][1000 genomes]
rs7757150	0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7759638	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7772415	0.82[AMR][1000 genomes]
rs911203	0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9295332	0.80[AMR][1000 genomes]
rs9295333	0.80[AMR][1000 genomes]
rs9295335	0.80[AMR][1000 genomes]
rs9347121	0.98[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[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	nsv886934	chr6:166642850-166747572	Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Enhancers Strong transcription Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	nsv886935	chr6:166704744-166726566	Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
3	nsv886936	chr6:166714024-166731289	Active TSS Enhancers Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region	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	chr6:166722600-166732800	Weak transcription	GM12878-XiMat	blood
2	chr6:166722600-166735600	Weak transcription	Brain Angular Gyrus	brain
3	chr6:166722800-166731200	Weak transcription	Spleen	Spleen
4	chr6:166723000-166731400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
5	chr6:166723000-166732000	Weak transcription	Gastric	stomach
6	chr6:166723200-166727200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr6:166723200-166732400	Weak transcription	Liver	Liver
8	chr6:166723200-166735400	Weak transcription	Brain Substantia Nigra	brain
9	chr6:166723200-166735600	Weak transcription	Brain Inferior Temporal Lobe	brain
10	chr6:166723200-166738800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
11	chr6:166723200-166744200	Weak transcription	Right Atrium	heart
12	chr6:166723600-166735800	Weak transcription	Brain Anterior Caudate	brain
13	chr6:166723800-166736000	Weak transcription	Brain Cingulate Gyrus	brain
14	chr6:166724200-166732400	Weak transcription	Primary B cells from peripheral blood	blood

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