Variant report

Variant	rs10994652
Chromosome Location	chr10:52594528-52594529
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 32 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs10994484	1.00[AMR][1000 genomes]
rs10994486	1.00[AMR][1000 genomes]
rs12241999	1.00[YRI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12242265	1.00[YRI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12245610	1.00[YRI][hapmap];0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12246868	1.00[AMR][1000 genomes]
rs12247876	1.00[YRI][hapmap];0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12248117	1.00[YRI][hapmap];0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12248603	1.00[AMR][1000 genomes]
rs12250671	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12250710	1.00[YRI][hapmap];0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12251965	1.00[AMR][1000 genomes]
rs12252902	1.00[YRI][hapmap];0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12254249	0.80[YRI][hapmap]
rs12255568	1.00[YRI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12256013	1.00[YRI][hapmap];1.00[AMR][1000 genomes]
rs12257587	1.00[YRI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12258558	1.00[AMR][1000 genomes]
rs12261175	1.00[AMR][1000 genomes]
rs12262186	1.00[YRI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12263224	1.00[YRI][hapmap];0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12266425	0.88[YRI][hapmap];0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12268784	1.00[YRI][hapmap];0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12268905	1.00[YRI][hapmap];0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16909340	1.00[AMR][1000 genomes]
rs4604823	1.00[AMR][1000 genomes]
rs7077103	1.00[YRI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7078064	1.00[AMR][1000 genomes]
rs7082887	0.88[YRI][hapmap];1.00[AMR][1000 genomes]
rs7094591	0.87[YRI][hapmap];1.00[AMR][1000 genomes]
rs7099856	1.00[YRI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][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	nsv1035197	chr10:52446582-52622349	Flanking Active TSS Active TSS Weak transcription Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	8 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	chr10:52576800-52597200	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr10:52580400-52643200	Weak transcription	Rectal Mucosa Donor 29	rectum
3	chr10:52581600-52595800	Weak transcription	Fetal Intestine Small	intestine
4	chr10:52585200-52617200	Weak transcription	Rectal Mucosa Donor 31	rectum
5	chr10:52592800-52598000	Genic enhancers	Liver	Liver
6	chr10:52593200-52596200	Strong transcription	Fetal Intestine Large	intestine
7	chr10:52593600-52594800	Strong transcription	Duodenum Mucosa	Duodenum
8	chr10:52594200-52599400	Weak transcription	HepG2	liver

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