Variant report

Variant	rs11209795
Chromosome Location	chr1:72027037-72027038
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs12043828	0.80[ASN][1000 genomes]
rs1607275	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs357206	0.81[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs357208	0.94[EUR][1000 genomes]
rs357209	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs357210	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs357211	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs357214	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs357216	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs672999	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv949599	chr1:71655652-72327802	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
2	nsv916508	chr1:71777392-72046388	Enhancers Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv546474	chr1:71793221-72040354	Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv1007250	chr1:71998391-72350683	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
5	nsv534992	chr1:71998391-72350683	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:72025200-72027200	Enhancers	Osteobl	bone
2	chr1:72026200-72027200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr1:72026400-72027400	Enhancers	Breast Myoepithelial Primary Cells	Breast
4	chr1:72026400-72028200	Enhancers	Muscle Satellite Cultured Cells	--
5	chr1:72026600-72027600	Enhancers	Rectal Smooth Muscle	rectum
6	chr1:72026600-72028200	Enhancers	NH-A	brain
7	chr1:72026800-72027600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
8	chr1:72026800-72029200	Enhancers	Colon Smooth Muscle	Colon
9	chr1:72027000-72028000	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr1:72027000-72028000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
11	chr1:72027000-72028000	Enhancers	NHDF-Ad	bronchial

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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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