Variant report

Variant	rs7790784
Chromosome Location	chr7:14802733-14802734
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 7 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:2)

rs_ID	r²[population]
rs217567	1.00[AMR][1000 genomes]
rs7805593	1.00[EUR][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	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
2	nsv1031041	chr7:14624127-14999201	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv538741	chr7:14624127-14999201	Enhancers Flanking Active TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv887712	chr7:14717872-14829858	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
5	nsv1020722	chr7:14792114-14871907	Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:14794800-14807000	Weak transcription	HUVEC	blood vessel
2	chr7:14800200-14802800	Enhancers	Fetal Heart	heart
3	chr7:14800200-14804200	Enhancers	Skeletal Muscle Female	skeletal muscle
4	chr7:14800800-14802800	Enhancers	Muscle Satellite Cultured Cells	--
5	chr7:14800800-14802800	Enhancers	Cortex derived primary cultured neurospheres	brain
6	chr7:14800800-14802800	Enhancers	Fetal Stomach	stomach
7	chr7:14801600-14802800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr7:14801600-14805000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
9	chr7:14801600-14807800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr7:14801800-14809000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr7:14801800-14809800	Weak transcription	Psoas Muscle	Psoas
12	chr7:14802000-14804200	Enhancers	Skeletal Muscle Male	skeletal muscle
13	chr7:14802000-14804800	Weak transcription	Left Ventricle	heart
14	chr7:14802000-14806400	Weak transcription	Rectal Smooth Muscle	rectum
15	chr7:14802200-14807000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr7:14802400-14802800	Weak transcription	Osteobl	bone
17	chr7:14802400-14805800	Weak transcription	NHDF-Ad	bronchial

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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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