Variant report

Variant	rs2255916
Chromosome Location	chr10:116999341-116999342
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 21 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs10749173	1.00[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs10885679	1.00[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs11197158	1.00[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs1264747	0.89[EUR][1000 genomes]
rs1268915	0.91[AFR][1000 genomes];0.89[EUR][1000 genomes]
rs1856357	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs1953758	1.00[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs2201364	1.00[AMR][1000 genomes]
rs2264063	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs2265929	0.81[AFR][1000 genomes];0.81[EUR][1000 genomes]
rs2492983	0.95[EUR][1000 genomes]
rs41314493	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs4409743	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs4752730	1.00[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs57236143	0.84[EUR][1000 genomes]
rs6585323	1.00[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7099807	0.87[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs7915481	0.95[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3435429	chr10:116394152-117006347	Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Strong transcription Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
2	nsv869279	chr10:116884639-117032437	Enhancers ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Strong transcription	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	nsv868940	chr10:116933802-117032437	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Strong transcription Flanking Bivalent TSS/Enh	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:116979600-117000200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr10:116981000-117010800	Weak transcription	Aorta	Aorta
3	chr10:116997200-117049800	Weak transcription	Ovary	ovary
4	chr10:116999200-117000400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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