Variant report

Variant	rs73833906
Chromosome Location	chr4:95335334-95335335
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr4:95334176..95336267-chr4:95337971..95340580,2	K562	blood:
2	chr4:95332786..95335416-chr4:95374983..95376965,3	K562	blood:
3	chr4:95333183..95336319-chr4:95372192..95375402,3	MCF-7	breast:
4	chr4:95331125..95332680-chr4:95333938..95335718,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000163110	Chromatin interaction

Extended variants
information (count: 5 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:2)

rs_ID	r²[population]
rs12643846	1.00[AFR][1000 genomes];0.82[ASN][1000 genomes]
rs73833915	0.82[ASN][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	nsv993495	chr4:94992315-95482578	Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
2	nsv594901	chr4:95254730-95493246	Flanking Active TSS Weak transcription Enhancers Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
3	nsv1003743	chr4:95255957-95469831	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:23 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:95328600-95335400	Weak transcription	Fetal Muscle Leg	muscle
2	chr4:95329200-95335800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
3	chr4:95333200-95335600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
4	chr4:95334000-95335400	Weak transcription	Left Ventricle	heart
5	chr4:95334000-95335400	Weak transcription	Psoas Muscle	Psoas
6	chr4:95334000-95335600	Weak transcription	HUES48 Cell Line	embryonic stem cell
7	chr4:95334000-95335800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
8	chr4:95334200-95335800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
9	chr4:95334200-95337200	Enhancers	Fetal Heart	heart
10	chr4:95334400-95335400	Enhancers	Skeletal Muscle Female	skeletal muscle
11	chr4:95334400-95335600	Weak transcription	HUES6 Cell Line	embryonic stem cell
12	chr4:95334400-95335800	Enhancers	Hela-S3	cervix
13	chr4:95334400-95335800	Enhancers	HSMMtube	muscle
14	chr4:95334400-95335800	Enhancers	Osteobl	bone
15	chr4:95334400-95336000	Enhancers	Skeletal Muscle Male	skeletal muscle
16	chr4:95334400-95346400	Weak transcription	Aorta	Aorta
17	chr4:95334600-95335600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr4:95334600-95335800	Enhancers	HepG2	liver
19	chr4:95334600-95337600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr4:95334800-95335800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
21	chr4:95334800-95336000	Enhancers	HUVEC	blood vessel
22	chr4:95335000-95335800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
23	chr4:95335000-95340600	Weak transcription	Liver	Liver

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