Variant report

Variant	rs4881298
Chromosome Location	chr10:4184635-4184636
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs11252377	0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12259410	0.83[AFR][1000 genomes];0.93[EUR][1000 genomes]
rs17350653	0.84[GIH][hapmap]
rs4881300	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs59778746	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs68154769	1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7071854	1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7913465	0.89[EUR][1000 genomes]
rs7923955	0.94[ASW][hapmap];1.00[CEU][hapmap];0.92[CHB][hapmap];1.00[CHD][hapmap];0.95[GIH][hapmap];0.82[JPT][hapmap];0.85[LWK][hapmap];1.00[MEX][hapmap];0.80[MKK][hapmap];0.96[TSI][hapmap];0.83[YRI][hapmap];0.88[AFR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][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	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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