Variant report

Variant	rs10736107
Chromosome Location	chr10:98123189-98123190
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 28 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs10748671	0.90[CEU][hapmap]
rs10748673	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[YRI][hapmap];0.90[AFR][1000 genomes];0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10786281	0.90[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10786282	1.00[CEU][hapmap];1.00[CHB][hapmap];0.82[JPT][hapmap];0.90[YRI][hapmap];0.90[AFR][1000 genomes];0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10882777	0.90[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10882778	0.90[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10882779	0.81[CEU][hapmap]
rs10882781	0.81[CEU][hapmap]
rs10882783	0.85[JPT][hapmap]
rs11188734	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs11188735	0.90[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11188736	0.90[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[EUR][1000 genomes];0.95[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]
rs2146392	0.90[CEU][hapmap]
rs2146394	0.82[JPT][hapmap]
rs2861572	1.00[JPT][hapmap]
rs2861576	0.82[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2901990	0.90[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs3789942	0.89[CHB][hapmap];1.00[JPT][hapmap]
rs3814223	0.84[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4917732	1.00[JPT][hapmap]
rs7077344	0.89[CHB][hapmap];1.00[JPT][hapmap];0.82[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:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:98106200-98126000	Weak transcription	Aorta	Aorta
2	chr10:98117000-98123800	Weak transcription	Right Atrium	heart
3	chr10:98117000-98134400	Weak transcription	Thymus	Thymus
4	chr10:98118800-98130200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
5	chr10:98120000-98125000	Weak transcription	Brain Angular Gyrus	brain
6	chr10:98120400-98125200	Weak transcription	Brain Substantia Nigra	brain
7	chr10:98121200-98125000	Weak transcription	Brain Cingulate Gyrus	brain
8	chr10:98121200-98126000	Weak transcription	Brain Anterior Caudate	brain
9	chr10:98121400-98125000	Weak transcription	Brain Hippocampus Middle	brain
10	chr10:98123000-98124200	Enhancers	Brain Inferior Temporal Lobe	brain

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links