Variant report

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

rs_ID	r²[population]
rs11751775	0.82[EUR][1000 genomes]
rs11755891	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11758564	0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12173971	0.91[EUR][1000 genomes]
rs12525747	0.85[EUR][1000 genomes]
rs12526777	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1321975	0.81[EUR][1000 genomes]
rs16900663	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16900676	0.91[EUR][1000 genomes]
rs17691995	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2031896	0.81[EUR][1000 genomes]
rs2296974	0.86[EUR][1000 genomes]
rs2296975	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2880923	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs3799093	0.84[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs3799094	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs58607458	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59783395	0.95[AFR][1000 genomes]
rs6912952	0.84[EUR][1000 genomes]
rs73471339	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73471350	0.84[AFR][1000 genomes];0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73475325	0.87[AFR][1000 genomes]
rs9346273	0.84[EUR][1000 genomes]
rs9351751	0.91[EUR][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	nsv886137	chr6:69684850-70095690	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv432919	chr6:69873179-70221322	Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv463149	chr6:70007450-70097588	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	nsv603635	chr6:70007450-70097588	Weak transcription Enhancers Flanking Active TSS Strong transcription	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:70049600-70080600	Weak transcription	Fetal Brain Male	brain
2	chr6:70054200-70066000	Weak transcription	Cortex derived primary cultured neurospheres	brain
3	chr6:70054400-70070800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
4	chr6:70054600-70098600	Weak transcription	Brain Anterior Caudate	brain
5	chr6:70054600-70100600	Weak transcription	Brain Angular Gyrus	brain
6	chr6:70054800-70080600	Weak transcription	Brain Inferior Temporal Lobe	brain
7	chr6:70059200-70083200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
8	chr6:70060000-70078200	Weak transcription	Fetal Lung	lung
9	chr6:70060200-70072200	Weak transcription	Brain Cingulate Gyrus	brain
10	chr6:70061400-70070800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr6:70063000-70080600	Weak transcription	Brain Germinal Matrix	brain
12	chr6:70065600-70066600	Strong transcription	Fetal Brain Female	brain
13	chr6:70066000-70066200	Strong transcription	Cortex derived primary cultured neurospheres	brain

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