Variant report

Variant	rs74069723
Chromosome Location	chr14:79784074-79784075
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 18 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs17109019	1.00[AMR][1000 genomes]
rs1868636	1.00[AMR][1000 genomes]
rs60679807	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61387635	1.00[AMR][1000 genomes]
rs7153825	1.00[AMR][1000 genomes]
rs7161402	1.00[AMR][1000 genomes]
rs74067963	1.00[AMR][1000 genomes]
rs74067968	1.00[AMR][1000 genomes]
rs74067969	1.00[AMR][1000 genomes]
rs74067991	1.00[AMR][1000 genomes]
rs74067995	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74067998	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74069731	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74069736	1.00[AMR][1000 genomes]
rs8004460	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv931412	chr14:79420297-79928269	Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv902110	chr14:79624492-79998294	Bivalent/Poised TSS Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv530072	chr14:79769657-79928269	Flanking Active TSS Enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:79773400-79791600	Weak transcription	Stomach Smooth Muscle	stomach
2	chr14:79781400-79784600	Weak transcription	Colon Smooth Muscle	Colon
3	chr14:79782800-79798400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
4	chr14:79783400-79785000	Enhancers	HUVEC	blood vessel
5	chr14:79784000-79784800	Enhancers	Placenta Amnion	Placenta Amnion

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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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