Variant report

Variant	rs34489871
Chromosome Location	chr6:163558679-163558680
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:6)

rs_ID	r²[population]
rs1033577	0.95[ASN][1000 genomes]
rs566126	0.92[ASN][1000 genomes]
rs6903059	0.81[EUR][1000 genomes]
rs9347728	0.85[EUR][1000 genomes]
rs9356098	0.86[EUR][1000 genomes]
rs9456837	0.93[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv917926	chr6:162646457-163609259	Enhancers Weak transcription Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	nsv932127	chr6:163000261-163950870	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
3	nsv1026490	chr6:163133433-163705708	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
4	nsv869286	chr6:163146342-163697445	Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
5	nsv916587	chr6:163337791-163606120	Enhancers Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
6	nsv886917	chr6:163507051-163573962	Enhancers Weak transcription Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:163550200-163561400	Weak transcription	Right Ventricle	heart
2	chr6:163556600-163559200	Enhancers	Fetal Brain Male	brain
3	chr6:163557800-163558800	Active TSS	Brain Hippocampus Middle	brain
4	chr6:163557800-163558800	Active TSS	Brain Substantia Nigra	brain
5	chr6:163557800-163559000	Active TSS	Brain Angular Gyrus	brain
6	chr6:163558000-163558800	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
7	chr6:163558000-163558800	Active TSS	Brain Cingulate Gyrus	brain
8	chr6:163558000-163558800	Active TSS	Brain Inferior Temporal Lobe	brain
9	chr6:163558000-163559000	Flanking Active TSS	Brain Germinal Matrix	brain
10	chr6:163558000-163559000	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
11	chr6:163558000-163559000	Active TSS	Fetal Brain Female	brain
12	chr6:163558400-163559200	Active TSS	Brain Anterior Caudate	brain

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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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