Variant report

Variant	rs60486756
Chromosome Location	chr2:231494110-231494111
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10169182	0.99[ASN][1000 genomes]
rs10804371	0.89[ASN][1000 genomes]
rs11680105	0.97[ASN][1000 genomes]
rs11885648	0.85[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs11885764	0.85[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs62194825	0.97[ASN][1000 genomes]
rs62194827	0.91[ASN][1000 genomes]
rs62194828	0.85[ASN][1000 genomes]
rs7369374	0.88[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv875955	chr2:231440555-231500805	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv527319	chr2:231492816-231501467	Enhancers Bivalent/Poised TSS Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:231472800-231497200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr2:231492800-231494200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr2:231493000-231494200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr2:231493000-231494400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr2:231493400-231497000	Weak transcription	Pancreas	Pancrea

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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