Variant report

Variant	rs7238073
Chromosome Location	chr18:29793212-29793213
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs16962851	1.00[ASW][hapmap];1.00[LWK][hapmap];0.85[MKK][hapmap];0.91[YRI][hapmap];0.92[AFR][1000 genomes]
rs16962889	0.82[AFR][1000 genomes]
rs28516907	0.82[AFR][1000 genomes]
rs28696064	1.00[AMR][1000 genomes]
rs7234401	0.90[YRI][hapmap];0.96[AFR][1000 genomes]
rs9945189	0.82[YRI][hapmap];0.86[AFR][1000 genomes]
rs9948293	0.82[ASW][hapmap];0.83[YRI][hapmap]
rs9948580	0.82[ASW][hapmap];0.83[YRI][hapmap]
rs9952703	0.82[YRI][hapmap]
rs9952884	0.82[AFR][1000 genomes]
rs9954412	0.91[YRI][hapmap];0.92[AFR][1000 genomes]
rs9955257	0.83[YRI][hapmap]
rs9959396	0.82[ASW][hapmap];0.83[YRI][hapmap]
rs9960121	0.90[AFR][1000 genomes]
rs9961328	1.00[ASW][hapmap];0.90[LWK][hapmap];0.83[YRI][hapmap]
rs9961628	1.00[ASW][hapmap];1.00[LWK][hapmap];0.85[MKK][hapmap];0.83[YRI][hapmap];0.86[AFR][1000 genomes]
rs9964636	0.82[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1056007	chr18:29711974-29899564	Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
2	nsv833616	chr18:29792336-29964212	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 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	chr18:29784600-29795200	Enhancers	Fetal Intestine Large	intestine
2	chr18:29786800-29795200	Enhancers	Fetal Intestine Small	intestine
3	chr18:29791800-29793600	Weak transcription	Rectal Mucosa Donor 31	rectum
4	chr18:29793000-29794600	Enhancers	HepG2	liver
5	chr18:29793200-29794400	Enhancers	Duodenum Mucosa	Duodenum
6	chr18:29793200-29794600	Enhancers	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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