Variant report

Variant	rs73855528
Chromosome Location	chr3:111237500-111237501
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs2675579	1.00[EUR][1000 genomes]
rs2698360	1.00[EUR][1000 genomes]
rs2932072	1.00[EUR][1000 genomes]
rs2950968	1.00[EUR][1000 genomes]
rs2950970	1.00[EUR][1000 genomes]
rs2950972	1.00[EUR][1000 genomes]
rs2971361	1.00[EUR][1000 genomes]
rs2971362	1.00[EUR][1000 genomes]
rs55768735	0.94[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs57101693	1.00[EUR][1000 genomes]
rs59852785	1.00[EUR][1000 genomes]
rs73852301	1.00[EUR][1000 genomes]
rs73852810	1.00[EUR][1000 genomes]
rs73855525	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs7633552	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv460821	chr3:110637471-111501097	Enhancers Active TSS Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Weak transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
2	nsv591275	chr3:110637471-111501097	Strong transcription Enhancers Weak transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
3	nsv997756	chr3:111226058-111376585	Active TSS Enhancers Strong transcription Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv3946	chr3:111236035-111283038	Flanking Active TSS Enhancers Weak transcription Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:111235600-111237800	Enhancers	Fetal Muscle Leg	muscle
2	chr3:111236400-111249600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr3:111236800-111238800	Enhancers	Stomach Mucosa	stomach
4	chr3:111237000-111242400	Weak transcription	Primary B cells from peripheral blood	blood
5	chr3:111237400-111238000	Enhancers	Small Intestine	intestine
6	chr3:111237400-111238200	Enhancers	Placenta	Placenta

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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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