Variant report

Variant	rs73380614
Chromosome Location	chr7:80632887-80632888
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 17 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs17154517	1.00[AMR][1000 genomes]
rs17154775	1.00[AMR][1000 genomes]
rs17154777	1.00[AMR][1000 genomes]
rs28578679	0.83[AFR][1000 genomes]
rs73136555	1.00[AMR][1000 genomes]
rs73372957	1.00[AMR][1000 genomes]
rs73372969	1.00[AMR][1000 genomes]
rs73372975	1.00[AMR][1000 genomes]
rs73372981	1.00[AMR][1000 genomes]
rs7791411	0.85[AFR][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	nsv888524	chr7:80107798-80723062	Active TSS Strong transcription Enhancers Genic enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
2	nsv1034690	chr7:80520004-80987682	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
3	nsv888549	chr7:80553950-80652059	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv888550	chr7:80584388-80644661	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	nsv5812	chr7:80601278-80645927	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
6	nsv521001	chr7:80618038-80644661	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
7	nsv888551	chr7:80620397-80723062	Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription ZNF genes & repeats	Chromatin interactive 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	chr7:80625400-80638200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr7:80631800-80633600	Enhancers	Breast Myoepithelial Primary Cells	Breast
3	chr7:80632000-80633000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr7:80632000-80633000	Weak transcription	Muscle Satellite Cultured Cells	--
5	chr7:80632000-80633200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr7:80632000-80633200	Weak transcription	Adipose Nuclei	Adipose
7	chr7:80632000-80633200	Weak transcription	HSMM	muscle
8	chr7:80632000-80633200	Weak transcription	NHDF-Ad	bronchial
9	chr7:80632400-80635000	Enhancers	Colon Smooth Muscle	Colon
10	chr7:80632600-80633000	Enhancers	Fetal Muscle Leg	muscle
11	chr7:80632600-80633200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr7:80632600-80634800	Enhancers	Fetal Brain Male	brain
13	chr7:80632800-80633200	Enhancers	Brain Germinal Matrix	brain
14	chr7:80632800-80633800	Enhancers	Fetal Brain Female	brain
15	chr7:80632800-80635800	Weak transcription	Rectal Smooth Muscle	rectum

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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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