Variant report

Variant	rs2991895
Chromosome Location	chr10:16276206-16276207
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 35 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs10159534	0.91[EUR][1000 genomes]
rs10737010	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs10737011	0.98[EUR][1000 genomes]
rs10752046	0.83[TSI][hapmap];0.80[EUR][1000 genomes]
rs10795356	0.87[EUR][1000 genomes]
rs10904693	0.95[EUR][1000 genomes]
rs1340133	0.91[EUR][1000 genomes]
rs1340134	1.00[EUR][1000 genomes]
rs1340137	0.94[EUR][1000 genomes]
rs1340138	0.94[EUR][1000 genomes]
rs1340139	0.94[EUR][1000 genomes]
rs1417093	1.00[EUR][1000 genomes]
rs1538762	0.97[EUR][1000 genomes]
rs1577073	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs1578266	0.87[EUR][1000 genomes]
rs1591933	0.98[EUR][1000 genomes]
rs1591934	0.89[EUR][1000 genomes]
rs1832657	0.89[EUR][1000 genomes]
rs1856726	0.98[EUR][1000 genomes]
rs2151948	0.95[EUR][1000 genomes]
rs2185386	0.91[EUR][1000 genomes]
rs2486896	0.94[EUR][1000 genomes]
rs2486906	0.89[EUR][1000 genomes]
rs2883626	0.98[EUR][1000 genomes]
rs4575155	0.90[EUR][1000 genomes]
rs4747265	0.86[EUR][1000 genomes]
rs6602081	0.89[EUR][1000 genomes]
rs6602082	0.87[EUR][1000 genomes]
rs6602088	0.91[EUR][1000 genomes]
rs7081816	0.87[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv530146	chr10:15722937-16522747	Active TSS Strong transcription Weak transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
2	nsv870420	chr10:16225427-16541252	Flanking Active TSS Strong transcription Enhancers Weak transcription Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
3	nsv894904	chr10:16233175-16477106	Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
4	nsv831796	chr10:16240111-16393044	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
5	nsv550018	chr10:16244094-16279015	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:16274800-16276800	Weak transcription	Fetal Brain Male	brain

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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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