Variant report

Variant	rs35969501
Chromosome Location	chr7:87721601-87721602
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 21 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs12535283	0.95[ASN][1000 genomes]
rs12537052	0.95[ASN][1000 genomes]
rs12538010	0.95[ASN][1000 genomes]
rs12704383	0.95[ASN][1000 genomes]
rs12704384	0.95[ASN][1000 genomes]
rs13222429	0.95[ASN][1000 genomes]
rs13230365	0.95[ASN][1000 genomes]
rs13234177	0.95[ASN][1000 genomes]
rs13234922	0.95[ASN][1000 genomes]
rs17150232	0.95[ASN][1000 genomes]
rs17255978	0.95[ASN][1000 genomes]
rs34957515	0.95[ASN][1000 genomes]
rs35345233	0.95[ASN][1000 genomes]
rs35532369	0.95[ASN][1000 genomes]
rs36004514	0.95[ASN][1000 genomes]
rs726329	0.95[ASN][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	nsv888677	chr7:86802025-87781111	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
2	nsv1015862	chr7:87075394-88049798	Bivalent/Poised TSS Flanking Active TSS Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
3	nsv1023352	chr7:87418818-88192925	Enhancers Weak transcription Strong transcription Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
4	nsv539005	chr7:87418818-88192925	Weak transcription ZNF genes & repeats Flanking Active TSS Enhancers Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
5	nsv525073	chr7:87535096-87812968	Strong transcription Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 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	chr7:87717800-87725400	Weak transcription	Fetal Muscle Leg	muscle
2	chr7:87718600-87722200	Enhancers	Fetal Lung	lung
3	chr7:87719200-87722200	Enhancers	Breast Myoepithelial Primary Cells	Breast
4	chr7:87719200-87722200	Enhancers	Adipose Nuclei	Adipose
5	chr7:87719400-87721800	Weak transcription	Fetal Brain Female	brain
6	chr7:87720400-87722200	Enhancers	Dnd41	blood
7	chr7:87720600-87721800	Enhancers	Brain Substantia Nigra	brain
8	chr7:87720600-87724200	Weak transcription	GM12878-XiMat	blood
9	chr7:87720600-87724400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
10	chr7:87720600-87731200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
11	chr7:87720800-87721800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr7:87721000-87724200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
13	chr7:87721400-87722000	Enhancers	Brain Cingulate Gyrus	brain
14	chr7:87721400-87723800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chr7:87721600-87722000	Enhancers	iPS-18 Cell Line	embryonic stem cell
16	chr7:87721600-87722200	Enhancers	Brain Hippocampus Middle	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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