Variant report

Variant	rs73651030
Chromosome Location	chr9:85685609-85685610
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 22 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs10429640	1.00[EUR][1000 genomes]
rs17085992	1.00[EUR][1000 genomes]
rs55999203	1.00[EUR][1000 genomes]
rs57254984	1.00[EUR][1000 genomes]
rs57845461	1.00[EUR][1000 genomes]
rs58019119	1.00[EUR][1000 genomes]
rs58084620	1.00[EUR][1000 genomes]
rs58273828	1.00[EUR][1000 genomes]
rs73651022	1.00[EUR][1000 genomes]
rs73651023	1.00[EUR][1000 genomes]
rs73651024	1.00[EUR][1000 genomes]
rs73651025	0.86[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73651026	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73651028	1.00[EUR][1000 genomes]
rs73651029	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73651031	1.00[EUR][1000 genomes]
rs73651032	1.00[EUR][1000 genomes]
rs73651038	1.00[EUR][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	nsv893511	chr9:85495968-85833127	Weak transcription Enhancers ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	nsv1043722	chr9:85663674-85747562	Enhancers Bivalent Enhancer ZNF genes & repeats Weak transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
3	nsv831642	chr9:85679425-85817338	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv831643	chr9:85679431-85798990	Enhancers Weak transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:85679200-85687800	Weak transcription	Fetal Intestine Small	intestine
2	chr9:85679800-85686600	Weak transcription	Rectal Mucosa Donor 29	rectum
3	chr9:85682200-85686000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr9:85682400-85706200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr9:85683600-85686400	Weak transcription	Pancreas	Pancrea
6	chr9:85683800-85687200	Weak transcription	Sigmoid Colon	Sigmoid Colon
7	chr9:85684000-85686600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr9:85684600-85686000	Enhancers	NHDF-Ad	bronchial
9	chr9:85684800-85685800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr9:85684800-85685800	Enhancers	Muscle Satellite Cultured Cells	--
11	chr9:85685000-85686600	Weak transcription	Rectal Mucosa Donor 31	rectum
12	chr9:85685000-85696600	Weak transcription	Cortex derived primary cultured neurospheres	brain
13	chr9:85685400-85685800	Enhancers	HMEC	breast
14	chr9:85685600-85686000	Enhancers	Osteobl	bone

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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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