Variant report

Variant	rs73723836
Chromosome Location	chr7:127814716-127814717
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:18)

rs_ID	r²[population]
rs56048330	1.00[AMR][1000 genomes]
rs56285353	1.00[AMR][1000 genomes]
rs57764135	1.00[AMR][1000 genomes]
rs59265323	1.00[AMR][1000 genomes]
rs712722	1.00[AMR][1000 genomes]
rs73455806	1.00[AMR][1000 genomes]
rs73721303	1.00[AMR][1000 genomes]
rs73723829	1.00[AMR][1000 genomes]
rs73723832	1.00[AMR][1000 genomes]
rs73723835	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73723837	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73723838	1.00[AMR][1000 genomes]
rs73723839	1.00[AMR][1000 genomes]
rs73723841	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73723842	1.00[AMR][1000 genomes]
rs7785591	1.00[AMR][1000 genomes]
rs791599	1.00[AMR][1000 genomes]
rs791615	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	nsv1022385	chr7:127246656-127971194	Weak transcription Bivalent Enhancer Enhancers Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
2	nsv539120	chr7:127246656-127971194	Enhancers Weak transcription Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
3	esv33413	chr7:127800064-127929303	Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	13 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:127808800-127821000	Weak transcription	Right Atrium	heart
2	chr7:127809200-127814800	Weak transcription	Spleen	Spleen
3	chr7:127810000-127818400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr7:127812400-127815200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr7:127814000-127815000	Enhancers	Primary B cells from peripheral blood	blood
6	chr7:127814200-127815000	Bivalent Enhancer	Primary hematopoietic stem cells short term culture	blood
7	chr7:127814200-127815400	Enhancers	Primary monocytes fromperipheralblood	blood
8	chr7:127814400-127814800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr7:127814400-127814800	Bivalent Enhancer	Placenta	Placenta
10	chr7:127814600-127814800	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain

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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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