Variant report

Variant	rs7768160
Chromosome Location	chr6:69370245-69370246
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

No data

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:69368749..69371635-chr6:69469945..69471663,2	K562	blood:
2	chr6:69367803..69371635-chr6:69469179..69471663,3	K562	blood:
3	chr6:69361875..69366635-chr6:69366839..69371569,10	K562	blood:
4	chr6:69351017..69353999-chr6:69369365..69372357,2	K562	blood:
5	chr6:69348595..69350906-chr6:69368329..69371179,2	K562	blood:
6	chr6:69369288..69371482-chr6:69451738..69454482,2	K562	blood:
7	chr6:69369127..69370671-chr6:69372780..69375655,2	K562	blood:
8	chr6:69364690..69367306-chr6:69368059..69370561,2	K562	blood:
9	chr6:69359484..69364655-chr6:69364836..69370262,9	K562	blood:

No data

No data

No data

Extended variants
information (count: 18 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs1983623	0.81[EUR][1000 genomes]
rs2064389	0.81[EUR][1000 genomes]
rs2257875	0.81[EUR][1000 genomes]
rs2585601	0.80[EUR][1000 genomes]
rs2585603	0.81[EUR][1000 genomes]
rs2746128	0.81[EUR][1000 genomes]
rs2880145	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4708197	0.82[EUR][1000 genomes]
rs4708231	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4708243	0.91[EUR][1000 genomes]
rs7746943	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7752462	0.95[EUR][1000 genomes]
rs7773117	0.84[EUR][1000 genomes]
rs9351732	0.81[EUR][1000 genomes]
rs9360357	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9363961	0.83[EUR][1000 genomes]
rs9363963	0.83[EUR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv886130	chr6:68950298-69531957	Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	14 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	chr6:69352200-69399000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr6:69364200-69399800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
3	chr6:69365800-69377400	Weak transcription	Cortex derived primary cultured neurospheres	brain
4	chr6:69367400-69371800	Weak transcription	Brain Angular Gyrus	brain
5	chr6:69367600-69370400	Weak transcription	Brain Substantia Nigra	brain
6	chr6:69367600-69377600	Weak transcription	Brain Inferior Temporal Lobe	brain
7	chr6:69367800-69371600	Weak transcription	Fetal Lung	lung
8	chr6:69368400-69371800	Weak transcription	Brain Anterior Caudate	brain
9	chr6:69368400-69377800	Weak transcription	Brain Cingulate Gyrus	brain
10	chr6:69368600-69376000	Weak transcription	K562	blood

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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