Variant report

Variant	rs7795366
Chromosome Location	chr7:137999519-137999520
allele	A/G
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]
rs1819966	0.89[EUR][1000 genomes]
rs28583294	0.85[EUR][1000 genomes]
rs55794944	0.89[EUR][1000 genomes]
rs55935714	0.81[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs56093444	0.90[EUR][1000 genomes]
rs56199969	0.91[EUR][1000 genomes]
rs56346792	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62488608	0.81[EUR][1000 genomes]
rs73157989	0.96[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs73159911	0.81[EUR][1000 genomes]
rs73159914	0.95[EUR][1000 genomes]
rs73159932	0.90[EUR][1000 genomes]
rs73162206	0.85[EUR][1000 genomes]
rs7457099	0.85[EUR][1000 genomes]
rs7778666	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7795878	0.83[AMR][1000 genomes];0.81[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	esv34048	chr7:137724092-138213119	Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	35 gene(s)	inside rSNPs	diseases
2	nsv831152	chr7:137884311-138033117	Flanking Active TSS Enhancers Active TSS Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
3	nsv1029101	chr7:137952620-138005671	Weak transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
4	nsv5967	chr7:137988239-138015844	Flanking Active TSS Weak transcription Enhancers Genic enhancers ZNF genes & repeats Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	nsv499698	chr7:137991842-138004097	Genic enhancers Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:137995200-138012000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr7:137998000-138000200	Enhancers	K562	blood
3	chr7:137998000-138000400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
4	chr7:137998200-137999800	Enhancers	Stomach Mucosa	stomach
5	chr7:137998600-137999600	Enhancers	Placenta	Placenta
6	chr7:137998600-138001600	Enhancers	HepG2	liver
7	chr7:137998600-138002400	Enhancers	Fetal Intestine Large	intestine
8	chr7:137999200-138000400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr7:137999200-138001000	Weak transcription	Liver	Liver
10	chr7:137999400-137999600	Genic enhancers	Fetal Intestine Small	intestine
11	chr7:137999400-138000400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr7:137999400-138000400	Enhancers	Duodenum Mucosa	Duodenum
13	chr7:137999400-138000600	Weak transcription	Sigmoid Colon	Sigmoid Colon

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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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