Variant report

Variant	rs12545937
Chromosome Location	chr8:69306475-69306476
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 36 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs1517129	1.00[ASN][1000 genomes]
rs1517130	1.00[ASN][1000 genomes]
rs16919092	0.94[ASN][1000 genomes]
rs16934487	0.83[ASN][1000 genomes]
rs16934503	0.87[ASN][1000 genomes]
rs16934507	0.87[ASN][1000 genomes]
rs16934510	0.87[ASN][1000 genomes]
rs16934533	0.89[AFR][1000 genomes]
rs16934546	0.92[AFR][1000 genomes]
rs16934555	0.89[AFR][1000 genomes]
rs1867633	0.90[ASN][1000 genomes]
rs2255882	1.00[ASN][1000 genomes]
rs2591019	1.00[ASN][1000 genomes]
rs2591020	1.00[ASN][1000 genomes]
rs2676648	0.96[ASN][1000 genomes]
rs2676649	1.00[ASN][1000 genomes]
rs2676650	1.00[ASN][1000 genomes]
rs2676652	1.00[ASN][1000 genomes]
rs2676654	1.00[ASN][1000 genomes]
rs2676656	1.00[ASN][1000 genomes]
rs58125593	0.88[ASN][1000 genomes]
rs59003086	0.87[ASN][1000 genomes]
rs59098392	0.90[ASN][1000 genomes]
rs59134336	0.90[ASN][1000 genomes]
rs59670612	0.87[ASN][1000 genomes]
rs61152394	0.86[ASN][1000 genomes]
rs6987210	0.83[AFR][1000 genomes]
rs6995683	0.87[AFR][1000 genomes]
rs6995713	0.89[AFR][1000 genomes]
rs7009700	0.89[AFR][1000 genomes]
rs7843010	0.89[AFR][1000 genomes]
rs7845014	0.92[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1028889	chr8:69026806-69308725	Weak transcription Enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv948687	chr8:69041121-69642540	Flanking Bivalent TSS/Enh Enhancers Weak transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
3	nsv1031040	chr8:69265471-69315554	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
4	nsv508512	chr8:69268794-69324532	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:69299400-69306800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
2	chr8:69306000-69307200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte 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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