Variant report

Variant	rs12100761
Chromosome Location	chr14:85830155-85830156
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 30 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs10134393	1.00[EUR][1000 genomes]
rs10136631	1.00[EUR][1000 genomes]
rs10136758	1.00[EUR][1000 genomes]
rs10138344	1.00[EUR][1000 genomes]
rs10141914	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10144184	0.80[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11846239	1.00[EUR][1000 genomes]
rs11848194	1.00[EUR][1000 genomes]
rs11850212	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11850250	1.00[EUR][1000 genomes]
rs140614	1.00[EUR][1000 genomes]
rs17121021	0.80[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17121060	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1951394	1.00[EUR][1000 genomes]
rs2182631	1.00[EUR][1000 genomes]
rs28402332	1.00[EUR][1000 genomes]
rs28680491	1.00[EUR][1000 genomes]
rs28706922	1.00[EUR][1000 genomes]
rs28729624	1.00[EUR][1000 genomes]
rs28833867	1.00[EUR][1000 genomes]
rs28871975	1.00[EUR][1000 genomes]
rs58358811	1.00[EUR][1000 genomes]
rs59459881	1.00[EUR][1000 genomes]
rs6574815	0.80[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs8022920	1.00[EUR][1000 genomes]
rs9323756	1.00[EUR][1000 genomes]
rs9972170	1.00[EUR][1000 genomes]
rs9972174	1.00[EUR][1000 genomes]
rs9972265	1.00[EUR][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	nsv1047924	chr14:85826280-85868228	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region lncRNA	2 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	chr14:85828800-85830200	Enhancers	Fetal Lung	lung
2	chr14:85829600-85830600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
3	chr14:85829800-85830400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr14:85829800-85830600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr14:85829800-85831000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived

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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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