Variant report

Variant	rs9619282
Chromosome Location	chr22:33030598-33030599
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	22:32920308-32927723..22:33024278-33030812	Hela-S3	cervix:

Variant related genes	Relation type
ENSG00000185666	Chromatin interaction

Extended variants
information (count: 28 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs12166424	1.00[CEU][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13340088	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13340089	1.00[CEU][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16990867	1.00[YRI][hapmap];0.92[AFR][1000 genomes];0.94[AMR][1000 genomes]
rs28373783	0.82[AMR][1000 genomes]
rs55771461	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs55904255	0.92[AFR][1000 genomes];0.94[AMR][1000 genomes]
rs56315097	0.88[AFR][1000 genomes];0.94[AMR][1000 genomes]
rs58007110	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs58659637	0.92[AFR][1000 genomes];0.94[AMR][1000 genomes]
rs7284915	1.00[YRI][hapmap];0.88[AFR][1000 genomes];0.94[AMR][1000 genomes]
rs7290002	0.91[AFR][1000 genomes];0.94[AMR][1000 genomes]
rs7290248	0.86[AFR][1000 genomes];0.89[AMR][1000 genomes]
rs7291390	0.88[AFR][1000 genomes];0.94[AMR][1000 genomes]
rs7291935	1.00[CEU][hapmap];0.95[YRI][hapmap];0.93[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73881769	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs8140105	1.00[CEU][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs8140208	0.86[AFR][1000 genomes];0.94[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs9619279	0.85[YRI][hapmap];0.82[AMR][1000 genomes]
rs9619285	1.00[CEU][hapmap]
rs9621511	1.00[CEU][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9621512	1.00[CEU][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1055541	chr22:33006967-33101138	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
2	esv2762119	chr22:33006967-33101150	Enhancers Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
3	nsv1061824	chr22:33013014-33101138	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Genic enhancers	TF binding region Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
4	nsv459875	chr22:33025180-33097662	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
5	nsv588896	chr22:33025180-33097662	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
6	nsv1064719	chr22:33028891-33159636	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Bivalent/Poised TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:33025400-33033200	Weak transcription	Fetal Kidney	kidney
2	chr22:33027600-33031000	Enhancers	Primary hematopoietic stem cells short term culture	blood
3	chr22:33028000-33030800	Enhancers	Adipose Nuclei	Adipose
4	chr22:33028800-33032400	Weak transcription	HepG2	liver
5	chr22:33029000-33032600	Weak transcription	Fetal Muscle Leg	muscle
6	chr22:33029000-33032600	Weak transcription	Placenta	Placenta
7	chr22:33029000-33039200	Weak transcription	Fetal Muscle Trunk	muscle
8	chr22:33029200-33032000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
9	chr22:33029200-33036000	Weak transcription	Fetal Stomach	stomach
10	chr22:33029400-33032400	Weak transcription	Fetal Thymus	thymus
11	chr22:33030000-33030600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr22:33030000-33030600	Enhancers	Primary hematopoietic stem cells	blood
13	chr22:33030000-33030800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr22:33030000-33031000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chr22:33030200-33030600	Enhancers	Primary monocytes fromperipheralblood	blood
16	chr22:33030200-33030800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr22:33030400-33031000	Weak transcription	Colon Smooth Muscle	Colon

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