Variant report

Variant	rs73631024
Chromosome Location	chr6:131133281-131133282
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 5 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:4)

rs_ID	r²[population]
rs2281488	0.94[AFR][1000 genomes]
rs73631023	0.86[AFR][1000 genomes]
rs73631030	1.00[AFR][1000 genomes]
rs73631092	1.00[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	nsv533971	chr6:130490694-131172051	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:131131200-131133600	Enhancers	HepG2	liver
2	chr6:131131800-131133400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
3	chr6:131132000-131138000	Weak transcription	Adipose Nuclei	Adipose
4	chr6:131132000-131141800	Weak transcription	Brain Anterior Caudate	brain
5	chr6:131132000-131159200	Weak transcription	HSMM	muscle
6	chr6:131132000-131173800	Weak transcription	HSMMtube	muscle
7	chr6:131133200-131133600	Flanking Active TSS	Liver	Liver

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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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