Variant report

Variant	rs6661527
Chromosome Location	chr1:170534655-170534656
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs10919435	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12038857	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12408432	0.80[EUR][1000 genomes]
rs12563881	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16863397	0.85[EUR][1000 genomes]
rs16863416	0.88[EUR][1000 genomes]
rs1928707	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6680284	0.82[EUR][1000 genomes]
rs71559505	0.89[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7519842	0.89[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9787312	0.83[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[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	nsv872543	chr1:170171083-170674903	Weak transcription Flanking Active TSS Enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
2	nsv533915	chr1:170258766-170725296	Enhancers Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:170531400-170535400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
2	chr1:170531400-170537600	Enhancers	NHDF-Ad	bronchial
3	chr1:170532200-170535000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr1:170532400-170535600	Enhancers	Osteobl	bone
5	chr1:170532600-170534800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr1:170532600-170535400	Enhancers	ES-I3 Cell Line	embryonic stem cell
7	chr1:170532800-170534800	Enhancers	Muscle Satellite Cultured Cells	--
8	chr1:170532800-170538600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr1:170533400-170535400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
10	chr1:170533400-170536800	Weak transcription	Fetal Muscle Leg	muscle
11	chr1:170533800-170535000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
12	chr1:170533800-170537400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
13	chr1:170534000-170537000	Weak transcription	HUES64 Cell Line	embryonic stem cell
14	chr1:170534200-170535200	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr1:170534400-170534800	Weak transcription	NHLF	lung
16	chr1:170534600-170534800	Enhancers	NH-A	brain

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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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