Variant report

Variant	rs3912641
Chromosome Location	chr12:10292657-10292658
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 3 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:2)

rs_ID	r²[population]
rs34083880	0.88[AFR][1000 genomes]
rs35366643	0.88[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	nsv898757	chr12:10229281-10614641	Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	48 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	chr12:10291400-10292800	Enhancers	Primary neutrophils fromperipheralblood	blood
2	chr12:10292200-10292800	Enhancers	Primary monocytes fromperipheralblood	blood
3	chr12:10292200-10292800	Enhancers	Monocytes-CD14+_RO01746	blood
4	chr12:10292400-10292800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr12:10292400-10292800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr12:10292400-10292800	Enhancers	Brain Angular Gyrus	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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