Variant report

Variant	rs7173752
Chromosome Location	chr15:75369760-75369761
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 10 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs16973530	0.80[YRI][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs58954461	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs59423613	1.00[AMR][1000 genomes]
rs73432970	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73438515	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73438534	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73438559	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][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	nsv569993	chr15:75242155-75483752	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	72 gene(s)	inside rSNPs	diseases
2	nsv457205	chr15:75336729-75447773	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
3	nsv569994	chr15:75336729-75447773	Genic enhancers Weak transcription Enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:75360000-75370000	Weak transcription	Right Atrium	heart
2	chr15:75369000-75371000	Enhancers	Primary neutrophils fromperipheralblood	blood
3	chr15:75369200-75369800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr15:75369200-75370600	Weak transcription	HepG2	liver
5	chr15:75369200-75371000	Enhancers	Monocytes-CD14+_RO01746	blood
6	chr15:75369400-75370400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
7	chr15:75369400-75370600	Enhancers	Primary B cells from cord blood	blood
8	chr15:75369600-75370400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr15:75369600-75370600	Enhancers	Primary hematopoietic stem cells	blood
10	chr15:75369600-75370600	Enhancers	HMEC	breast
11	chr15:75369600-75370800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr15:75369600-75370800	Enhancers	Primary monocytes fromperipheralblood	blood
13	chr15:75369600-75370800	Enhancers	Primary B cells from peripheral blood	blood
14	chr15:75369600-75370800	Enhancers	GM12878-XiMat	blood

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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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