Variant report

Variant	rs2637314
Chromosome Location	chr10:27983331-27983332
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 47 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:45)

rs_ID	r²[population]
rs11015959	0.90[ASN][1000 genomes]
rs11015961	0.80[ASN][1000 genomes]
rs1907386	0.83[EUR][1000 genomes]
rs1907390	0.90[EUR][1000 genomes]
rs1907391	0.90[EUR][1000 genomes]
rs1907392	0.89[EUR][1000 genomes]
rs2246903	0.98[AFR][1000 genomes];0.80[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs2252651	0.82[EUR][1000 genomes]
rs2451915	0.90[EUR][1000 genomes]
rs2451916	0.97[AFR][1000 genomes];0.90[EUR][1000 genomes]
rs2451917	0.90[EUR][1000 genomes]
rs2451919	0.89[EUR][1000 genomes]
rs2451920	0.88[EUR][1000 genomes]
rs2492911	0.92[EUR][1000 genomes]
rs2492912	0.90[EUR][1000 genomes]
rs2492913	0.89[EUR][1000 genomes]
rs2492914	0.89[EUR][1000 genomes]
rs2492915	0.90[EUR][1000 genomes]
rs2492916	0.89[EUR][1000 genomes]
rs2492917	0.88[EUR][1000 genomes]
rs2637293	0.83[EUR][1000 genomes]
rs2637297	0.83[EUR][1000 genomes]
rs2637303	0.90[EUR][1000 genomes]
rs2637304	0.90[EUR][1000 genomes]
rs2637327	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs2637328	0.88[EUR][1000 genomes]
rs2815477	0.85[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2815478	0.83[EUR][1000 genomes]
rs2815479	0.83[EUR][1000 genomes]
rs2815559	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2815560	0.90[EUR][1000 genomes]
rs2815561	0.97[AFR][1000 genomes];0.90[EUR][1000 genomes]
rs2815562	0.90[EUR][1000 genomes]
rs2815564	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs2815565	0.90[EUR][1000 genomes]
rs2815566	0.93[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs2815569	0.89[EUR][1000 genomes]
rs2815570	0.89[EUR][1000 genomes]
rs2815571	0.89[EUR][1000 genomes]
rs2815573	0.89[EUR][1000 genomes]
rs2815574	0.87[EUR][1000 genomes]
rs2815575	0.87[EUR][1000 genomes]
rs2815576	0.87[EUR][1000 genomes]
rs2815577	0.86[EUR][1000 genomes]
rs2999980	0.89[EUR][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	nsv550241	chr10:27569521-28025771	Enhancers ZNF genes & repeats Strong transcription Weak transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
2	esv3368825	chr10:27864181-28043820	Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:27982200-27983800	Weak transcription	Ovary	ovary
2	chr10:27982200-27984000	Weak transcription	Aorta	Aorta
3	chr10:27982200-27984600	Weak transcription	Colon Smooth Muscle	Colon
4	chr10:27982400-27984000	Weak transcription	Rectal Smooth Muscle	rectum
5	chr10:27982400-27984000	Weak transcription	Stomach Smooth Muscle	stomach
6	chr10:27982400-27988800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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