Variant report

Variant	rs73401506
Chromosome Location	chr22:33265501-33265502
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	22:31936958-31958600..22:33262063-33266567	K562	blood:
2	22:32846948-32860159..22:33262063-33266567	Hela-S3	cervix:

Variant related genes	Relation type
ENSG00000214093	Chromatin interaction
ENSG00000184459	Chromatin interaction

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs59856303	1.00[AMR][1000 genomes]
rs73158368	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73401508	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73401512	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73403237	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73403252	1.00[AMR][1000 genomes]
rs73403269	1.00[AMR][1000 genomes]
rs73405263	1.00[AMR][1000 genomes]
rs73405271	1.00[AMR][1000 genomes]
rs73408552	1.00[AMR][1000 genomes]
rs73408571	1.00[AMR][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	nsv3599	chr22:33230106-33274789	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
2	nsv1059368	chr22:33249121-33268782	Genic enhancers Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:21 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:33227000-33272400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
2	chr22:33237400-33282200	Weak transcription	Fetal Brain Female	brain
3	chr22:33256400-33269400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr22:33257800-33269600	Weak transcription	Fetal Intestine Small	intestine
5	chr22:33257800-33270000	Weak transcription	Fetal Intestine Large	intestine
6	chr22:33257800-33282000	Weak transcription	HepG2	liver
7	chr22:33258200-33266600	Weak transcription	H9 Cell Line	embryonic stem cell
8	chr22:33258400-33266800	Weak transcription	Aorta	Aorta
9	chr22:33258400-33267200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
10	chr22:33259000-33265800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr22:33259000-33270800	Weak transcription	Fetal Lung	lung
12	chr22:33259400-33270200	Weak transcription	Fetal Muscle Trunk	muscle
13	chr22:33261200-33270400	Weak transcription	H1 Cell Line	embryonic stem cell
14	chr22:33262000-33265800	Weak transcription	HUES6 Cell Line	embryonic stem cell
15	chr22:33262200-33266600	Weak transcription	HUES64 Cell Line	embryonic stem cell
16	chr22:33262600-33266600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
17	chr22:33263200-33268600	Weak transcription	K562	blood
18	chr22:33263400-33267200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
19	chr22:33264400-33265600	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
20	chr22:33265200-33269400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr22:33265200-33282000	Weak transcription	HUES48 Cell Line	embryonic stem cell

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