Variant report

Variant	rs12243807
Chromosome Location	chr10:4184768-4184769
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 20 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs11252363	0.85[CEU][hapmap]
rs11252364	0.85[CEU][hapmap]
rs12244138	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12247651	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17257066	0.87[CEU][hapmap]
rs17258608	0.85[CEU][hapmap]
rs17258741	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1998329	0.83[EUR][1000 genomes]
rs55640115	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs68172044	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72776543	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72776549	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72776555	0.95[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs72776556	0.92[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7897041	0.82[CEU][hapmap];0.80[EUR][1000 genomes]
rs7912112	0.82[CEU][hapmap];0.80[EUR][1000 genomes]
rs9732075	0.87[CEU][hapmap]

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	nsv1051297	chr10:3908706-4277678	Enhancers Active TSS Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	13 gene(s)	inside rSNPs	diseases
2	nsv831772	chr10:4039292-4212218	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	esv3427419	chr10:4184576-4184815	Weak transcription	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	chr10:4174800-4187000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr10:4184000-4187000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr10:4184200-4193600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr10:4184400-4187200	Weak transcription	Esophagus	oesophagus
5	chr10:4184400-4187200	Weak transcription	Gastric	stomach

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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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