Variant report

Variant	rs66487667
Chromosome Location	chr11:71277273-71277274
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Variant related genes	Relation type
ENSG00000248903	TF binding region
ENSG00000172890	Chromatin interaction
ENSG00000172893	Chromatin interaction
ENSG00000254682	Chromatin interaction

Extended variants
information (count: 12 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:5)

rs_ID	r²[population]
rs10898311	0.88[ASN][1000 genomes]
rs10898312	0.90[ASN][1000 genomes]
rs11234188	0.81[AMR][1000 genomes]
rs11234193	0.84[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs11234218	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv530623	chr11:71088949-72020418	Enhancers Transcr. at gene 5' and 3' Active TSS Strong transcription Bivalent Enhancer Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	134 gene(s)	inside rSNPs	diseases
2	nsv468632	chr11:71200320-71289089	Weak transcription Enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
3	nsv555402	chr11:71200320-71289089	Strong transcription Weak transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
4	esv3372246	chr11:71223101-71435819	Strong transcription Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
5	nsv897899	chr11:71234107-71277981	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Active TSS	TF binding region CpG island Chromatin interactive region	8 gene(s)	inside rSNPs	diseases
6	nsv983039	chr11:71268641-71277624	Enhancers Weak transcription Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
7	nsv825988	chr11:71277262-71294289	ZNF genes & repeats Weak transcription Flanking Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:18 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:71274800-71277400	Weak transcription	Brain Substantia Nigra	brain
2	chr11:71275200-71277400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
3	chr11:71275400-71277600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr11:71276200-71277600	Enhancers	Breast Myoepithelial Primary Cells	Breast
5	chr11:71276400-71277400	Enhancers	Primary hematopoietic stem cells short term culture	blood
6	chr11:71276600-71278200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
7	chr11:71276800-71277600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr11:71277000-71277400	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
9	chr11:71277000-71277400	Enhancers	HMEC	breast
10	chr11:71277000-71279200	Enhancers	HUES6 Cell Line	embryonic stem cell
11	chr11:71277200-71277400	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr11:71277200-71277600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr11:71277200-71277600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr11:71277200-71277600	Enhancers	Left Ventricle	heart
15	chr11:71277200-71277800	Enhancers	Fetal Brain Male	brain
16	chr11:71277200-71278000	Bivalent Enhancer	Fetal Stomach	stomach
17	chr11:71277200-71278200	Enhancers	Spleen	Spleen
18	chr11:71277200-71280400	Enhancers	Adipose Nuclei	Adipose

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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