Variant report

Variant	rs7673632
Chromosome Location	chr4:74695534-74695535
allele	C/T
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:19)

rs_ID	r²[population]
rs10033377	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16849925	1.00[EUR][1000 genomes]
rs1951237	1.00[EUR][1000 genomes]
rs2227525	1.00[EUR][1000 genomes]
rs2227532	1.00[TSI][hapmap];1.00[EUR][1000 genomes]
rs2227545	1.00[EUR][1000 genomes]
rs28544060	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28560265	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28707294	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28879705	1.00[EUR][1000 genomes]
rs55648028	1.00[EUR][1000 genomes]
rs59569175	1.00[EUR][1000 genomes]
rs6840833	1.00[EUR][1000 genomes]
rs6847987	1.00[EUR][1000 genomes]
rs6853880	1.00[EUR][1000 genomes]
rs73827899	1.00[EUR][1000 genomes]
rs73827900	1.00[EUR][1000 genomes]
rs7657469	1.00[EUR][1000 genomes]
rs7668660	1.00[ASW][hapmap];1.00[GIH][hapmap];0.81[LWK][hapmap];1.00[MEX][hapmap];1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1001725	chr4:74354050-74860924	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
2	nsv530126	chr4:74376622-74843892	Bivalent Enhancer Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Active TSS Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:18 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:74689200-74698000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
2	chr4:74693400-74696200	Enhancers	Primary neutrophils fromperipheralblood	blood
3	chr4:74693800-74697800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr4:74694400-74695600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr4:74694600-74695600	Enhancers	Primary hematopoietic stem cells short term culture	blood
6	chr4:74694800-74698800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr4:74695000-74695600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr4:74695000-74696000	Weak transcription	NHDF-Ad	bronchial
9	chr4:74695000-74697000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr4:74695000-74697200	Weak transcription	Osteobl	bone
11	chr4:74695000-74698000	Weak transcription	Primary hematopoietic stem cells	blood
12	chr4:74695000-74698000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr4:74695200-74697400	Weak transcription	HMEC	breast
14	chr4:74695200-74697800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
15	chr4:74695200-74697800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
16	chr4:74695200-74701800	Weak transcription	Monocytes-CD14+_RO01746	blood
17	chr4:74695400-74697800	Weak transcription	Muscle Satellite Cultured Cells	--
18	chr4:74695400-74702000	Weak transcription	Primary monocytes fromperipheralblood	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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