Variant report

Variant	rs10260511
Chromosome Location	chr7:14237240-14237241
allele	A/C
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:8)

rs_ID	r²[population]
rs10229939	0.83[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10252500	0.86[EUR][1000 genomes]
rs10274998	0.88[CEU][hapmap];0.81[CHB][hapmap];0.95[JPT][hapmap];0.93[TSI][hapmap];0.84[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10275304	0.81[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2108203	0.80[AMR][1000 genomes];0.87[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6949500	0.88[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap];0.93[TSI][hapmap];0.84[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6949565	0.83[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6967846	0.82[ASW][hapmap];0.88[CEU][hapmap];0.86[CHB][hapmap];0.95[JPT][hapmap];0.85[TSI][hapmap];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[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	nsv949467	chr7:13938464-14279074	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv949033	chr7:14086106-14860323	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv1015312	chr7:14092753-14266917	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv1021056	chr7:14162525-14269443	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	nsv1025437	chr7:14226741-14295671	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:14233600-14237800	Enhancers	Cortex derived primary cultured neurospheres	brain
2	chr7:14233800-14238000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr7:14235400-14237600	Enhancers	Muscle Satellite Cultured Cells	--
4	chr7:14235600-14237400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr7:14235600-14237600	Enhancers	HSMMtube	muscle
6	chr7:14235600-14237800	Enhancers	HSMM	muscle
7	chr7:14235800-14237600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
8	chr7:14235800-14237600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
9	chr7:14236400-14237600	Enhancers	Brain Germinal Matrix	brain
10	chr7:14236400-14237800	Enhancers	Fetal Heart	heart
11	chr7:14236600-14237400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
12	chr7:14236600-14237600	Enhancers	Adipose Nuclei	Adipose
13	chr7:14236800-14237600	Enhancers	Brain Angular Gyrus	brain
14	chr7:14237000-14237400	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr7:14237000-14237600	Enhancers	Brain Inferior Temporal Lobe	brain

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dbSNP/dbVar ID: rs12345 /nsv7879
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