Variant report

Variant	rs2562810
Chromosome Location	chr2:191005265-191005266
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 22 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs1072068	0.90[AFR][1000 genomes]
rs12693562	0.92[AFR][1000 genomes]
rs12693563	0.90[AFR][1000 genomes]
rs1366673	0.90[AFR][1000 genomes]
rs1366675	0.88[AFR][1000 genomes]
rs1806355	0.90[AFR][1000 genomes]
rs2562803	0.90[AFR][1000 genomes]
rs2562804	0.80[AFR][1000 genomes]
rs2562807	0.90[AFR][1000 genomes]
rs2562808	0.90[AFR][1000 genomes]
rs2562809	0.90[AFR][1000 genomes]
rs2562811	0.90[AFR][1000 genomes]
rs2562812	0.90[AFR][1000 genomes]
rs2562813	0.89[AFR][1000 genomes]
rs2562814	0.89[AFR][1000 genomes]
rs2562815	0.88[AFR][1000 genomes]
rs2562816	0.90[AFR][1000 genomes]
rs2562817	0.90[AFR][1000 genomes]
rs2690727	0.90[AFR][1000 genomes]
rs2690728	0.82[AFR][1000 genomes]
rs2690729	0.90[AFR][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	esv3439178	chr2:190877215-191124499	Enhancers Weak transcription ZNF genes & repeats Active TSS Strong transcription Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:190996600-191008200	Weak transcription	Aorta	Aorta
2	chr2:190997000-191006200	Weak transcription	Psoas Muscle	Psoas
3	chr2:191004800-191005400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
4	chr2:191004800-191006800	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast

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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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