Variant report

Variant	rs73651028
Chromosome Location	chr9:85682422-85682423
allele	A/G
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	1.00[EUR][1000 genomes]
rs73651026	1.00[EUR][1000 genomes]
rs73651029	1.00[EUR][1000 genomes]
rs73651030	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:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:85679200-85687800	Weak transcription	Fetal Intestine Small	intestine
2	chr9:85679400-85684200	Weak transcription	Rectal Mucosa Donor 31	rectum
3	chr9:85679800-85686600	Weak transcription	Rectal Mucosa Donor 29	rectum
4	chr9:85681000-85682600	Enhancers	Muscle Satellite Cultured Cells	--
5	chr9:85681000-85683200	Weak transcription	Pancreas	Pancrea
6	chr9:85681000-85685000	Strong transcription	Cortex derived primary cultured neurospheres	brain
7	chr9:85681200-85683400	Weak transcription	Stomach Mucosa	stomach
8	chr9:85682200-85684400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr9:85682200-85684800	Weak transcription	HMEC	breast
10	chr9:85682200-85686000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
11	chr9:85682400-85683400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr9:85682400-85684600	Weak transcription	NH-A	brain
13	chr9:85682400-85684600	Weak transcription	NHDF-Ad	bronchial
14	chr9:85682400-85684800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
15	chr9:85682400-85685600	Weak transcription	Osteobl	bone
16	chr9:85682400-85706200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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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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