Variant report

Variant	rs62473733
Chromosome Location	chr8:3328082-3328083
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr8:3328036-3328126	K562	blood:	n/a	n/a

Variant related genes	Relation type
CSMD1	TF binding region

Extended variants
information (count: 35 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs10093282	1.00[ASN][1000 genomes]
rs10097790	1.00[ASN][1000 genomes]
rs10102356	1.00[ASN][1000 genomes]
rs10112195	1.00[ASN][1000 genomes]
rs10282987	1.00[ASN][1000 genomes]
rs10283040	1.00[ASN][1000 genomes]
rs10283217	1.00[ASN][1000 genomes]
rs10283244	1.00[ASN][1000 genomes]
rs28419735	1.00[ASN][1000 genomes]
rs28525416	1.00[ASN][1000 genomes]
rs28548672	1.00[ASN][1000 genomes]
rs28582416	1.00[ASN][1000 genomes]
rs28608554	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28711878	1.00[ASN][1000 genomes]
rs28736728	1.00[ASN][1000 genomes]
rs62473731	0.89[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs62473735	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62505627	1.00[ASN][1000 genomes]
rs62505629	1.00[ASN][1000 genomes]
rs62505643	1.00[ASN][1000 genomes]
rs62505646	1.00[ASN][1000 genomes]
rs73497425	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:13 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1025209	chr8:3067655-3754882	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv1026998	chr8:3102679-3593264	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv1034076	chr8:3168033-3989947	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv539351	chr8:3168033-3989947	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
5	nsv1017164	chr8:3174168-4026811	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
6	nsv539352	chr8:3174168-4026811	Enhancers Active TSS Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
7	nsv1018218	chr8:3180287-4089011	Active TSS Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
8	nsv1034838	chr8:3307014-3413573	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
9	nsv1028613	chr8:3315493-3339898	Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats	TF binding region CpG island	1 gene(s)	inside rSNPs	diseases
10	nsv1028926	chr8:3318340-3667389	Enhancers Active TSS ZNF genes & repeats Weak transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
11	nsv539353	chr8:3318340-3667389	Enhancers Active TSS ZNF genes & repeats Weak transcription Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
12	nsv465344	chr8:3319748-3333127	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	inside rSNPs	diseases
13	nsv609737	chr8:3319748-3333127	Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Active TSS	TF binding region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:3324600-3328200	Enhancers	Brain Angular Gyrus	brain
2	chr8:3326000-3328200	Enhancers	Brain Inferior Temporal Lobe	brain
3	chr8:3326000-3328400	Enhancers	Cortex derived primary cultured neurospheres	brain
4	chr8:3326600-3328200	Weak transcription	Brain Substantia Nigra	brain
5	chr8:3326800-3328200	Enhancers	Fetal Brain Male	brain
6	chr8:3327600-3328400	Enhancers	Brain Anterior Caudate	brain
7	chr8:3327600-3328600	Enhancers	Brain Hippocampus Middle	brain
8	chr8:3327800-3328600	Weak transcription	Brain Cingulate Gyrus	brain

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