Variant report

Variant	rs73717535
Chromosome Location	chr7:111999062-111999063
allele	A/G
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:14)

rs_ID	r²[population]
rs11976430	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs34571830	0.93[AFR][1000 genomes]
rs55731771	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs55780403	1.00[AMR][1000 genomes]
rs61142815	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73715502	0.93[AFR][1000 genomes]
rs73717512	1.00[AFR][1000 genomes]
rs73717517	1.00[AFR][1000 genomes]
rs73717527	1.00[AFR][1000 genomes];0.89[EUR][1000 genomes]
rs73717530	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs73717532	0.93[AFR][1000 genomes]
rs73717533	0.93[AFR][1000 genomes]
rs73717543	0.87[AFR][1000 genomes]
rs73717548	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv532335	chr7:111411990-112054905	Enhancers Strong transcription Flanking Active TSS Weak transcription ZNF genes & repeats Genic enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
2	nsv531436	chr7:111856171-112585407	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	105 gene(s)	inside rSNPs	diseases
3	nsv1020212	chr7:111944370-112032596	Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:111966600-112000800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr7:111983800-112004600	Weak transcription	Pancreas	Pancrea
3	chr7:111987800-112000800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr7:111993400-111999400	Weak transcription	Right Atrium	heart
5	chr7:111995800-112000800	Weak transcription	Aorta	Aorta
6	chr7:111998600-112006600	Enhancers	Breast Myoepithelial Primary Cells	Breast
7	chr7:111999000-112000600	Weak transcription	Stomach Smooth Muscle	stomach
8	chr7:111999000-112000600	Weak transcription	HepG2	liver

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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