Variant report

Variant	rs10786281
Chromosome Location	chr10:98116936-98116937
allele	C/T
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	BHLHE40	chr10:98116770-98116936	HepG2	liver:	n/a	n/a
2	ZNF263	chr10:98116780-98116980	HEK293-T-REx	kidney:	n/a	n/a

Variant related genes	Relation type
OPALIN	TF binding region

Extended variants
information (count: 27 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs10736107	0.82[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10748671	0.81[CEU][hapmap]
rs10748673	0.90[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10786282	0.90[CEU][hapmap];1.00[CHB][hapmap];0.82[JPT][hapmap];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10882777	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10882778	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10882779	0.90[CEU][hapmap];0.92[YRI][hapmap];0.95[AFR][1000 genomes];0.83[EUR][1000 genomes]
rs10882781	0.90[CEU][hapmap];0.81[EUR][1000 genomes]
rs10882783	0.85[JPT][hapmap]
rs11188734	0.90[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[YRI][hapmap];0.81[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs11188735	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11188736	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[YRI][hapmap];0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11593074	0.82[JPT][hapmap]
rs11818883	0.89[CHB][hapmap];1.00[JPT][hapmap]
rs11818896	0.89[CHB][hapmap];1.00[JPT][hapmap]
rs11818942	0.89[CHB][hapmap]
rs1923708	0.82[JPT][hapmap]
rs2146394	0.82[JPT][hapmap]
rs2861572	1.00[JPT][hapmap]
rs2861576	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2901990	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3789942	0.89[CHB][hapmap];1.00[JPT][hapmap]
rs3814223	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap];1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4917732	1.00[JPT][hapmap]
rs7077344	0.89[CHB][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3413353	chr10:98039370-98561524	Enhancers Genic enhancers Weak transcription Strong transcription Active TSS Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
2	nsv831950	chr10:98080972-98245434	Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	7 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	chr10:98106200-98126000	Weak transcription	Aorta	Aorta
2	chr10:98114800-98117000	Strong transcription	Thymus	Thymus
3	chr10:98115000-98119000	Active TSS	Brain Anterior Caudate	brain
4	chr10:98115200-98119600	Active TSS	Brain Angular Gyrus	brain
5	chr10:98116000-98118800	Active TSS	Brain Hippocampus Middle	brain
6	chr10:98116400-98117200	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
7	chr10:98116400-98118800	Active TSS	Brain Inferior Temporal Lobe	brain
8	chr10:98116600-98117000	Flanking Active TSS	Brain Cingulate Gyrus	brain
9	chr10:98116600-98117600	Bivalent/Poised TSS	Brain Dorsolateral Prefrontal Cortex	brain
10	chr10:98116800-98117000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr10:98116800-98117000	Enhancers	Pancreas	Pancrea
12	chr10:98116800-98117000	Enhancers	Right Atrium	heart
13	chr10:98116800-98117200	Enhancers	Brain Substantia Nigra	brain

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