Variant report

Variant	rs11170565
Chromosome Location	chr12:39461094-39461095
allele	A/G
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:10)

rs_ID	r²[population]
rs11170524	0.92[ASN][1000 genomes]
rs11170641	0.91[ASN][1000 genomes]
rs11561416	0.91[ASN][1000 genomes]
rs12230119	0.92[ASN][1000 genomes]
rs12826889	0.91[ASN][1000 genomes]
rs1463212	0.89[ASN][1000 genomes]
rs1562727	0.88[ASN][1000 genomes]
rs1900991	0.91[ASN][1000 genomes]
rs2388173	0.91[ASN][1000 genomes]
rs7300430	0.91[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	nsv1047623	chr12:39187817-39539939	Active TSS Bivalent Enhancer Weak transcription Flanking Active TSS ZNF genes & repeats Enhancers Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
2	esv21411	chr12:39458222-39478357	Enhancers Flanking Active TSS Weak transcription Active TSS	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:39455400-39463000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr12:39458800-39462400	Enhancers	Primary monocytes fromperipheralblood	blood
3	chr12:39459200-39461800	Enhancers	Monocytes-CD14+_RO01746	blood
4	chr12:39461000-39462400	Enhancers	Primary neutrophils fromperipheralblood	blood

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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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