Variant report

Variant	rs7287435
Chromosome Location	chr22:32476600-32476601
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:15)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr22:32372870..32373842-chr22:32476568..32477785,13	MCF-7	breast:
2	chr22:32372869..32373942-chr22:32475953..32477559,5	K562	blood:
3	22:32162110-32166713..22:32475239-32477762	Hela-S3	cervix:
4	22:32475239-32477762..22:32860159-32865649	GM12878	blood:
5	22:32338420-32342898..22:32475239-32477762	Hela-S3	cervix:
6	22:32475239-32477762..22:32764253-32784733	Hela-S3	cervix:
7	chr22:32372925..32373819-chr22:32476594..32477554,6	MCF-7	breast:
8	22:32170492-32188129..22:32475239-32477762	Hela-S3	cervix:
9	22:32264718-32278135..22:32475239-32477762	Hela-S3	cervix:
10	22:32053085-32061138..22:32475239-32477762	GM12878	blood:
11	22:32475239-32477762..22:33452523-33459358	GM12878	blood:
12	22:31836635-31847259..22:32475239-32477762	Hela-S3	cervix:
13	22:32102727-32109893..22:32475239-32477762	Hela-S3	cervix:
14	22:32475239-32477762..22:32920308-32927723	Hela-S3	cervix:
15	22:32475239-32477762..22:32750950-32761732	Hela-S3	cervix:

(count:1 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-YWHAH-6	chr22:32476591-32476801	ucscGeneNc_uc003anh_2

No data

Variant related genes	Relation type
ENSG00000128254	Chromatin interaction
ENSG00000100150	Chromatin interaction
ENSG00000243519	Chromatin interaction
ENSG00000183530	Chromatin interaction
ENSG00000241954	Chromatin interaction
ENSG00000271093	Chromatin interaction
ENSG00000232218	Chromatin interaction
ENSG00000184459	Chromatin interaction
ENSG00000185666	Chromatin interaction
ENSG00000241878	Chromatin interaction
ENSG00000128245	Chromatin interaction
ENSG00000230736	Chromatin interaction
ENSG00000128276	Chromatin interaction
ENSG00000205853	Chromatin interaction
ENSG00000184708	Chromatin interaction

Extended variants
information (count: 39 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs1076905	1.00[JPT][hapmap]
rs1076906	1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs11089537	0.86[ASN][1000 genomes]
rs12159428	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12160839	1.00[JPT][hapmap];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2006233	1.00[CHD][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs2006253	1.00[CHD][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs28590200	0.97[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs55920759	0.86[ASN][1000 genomes]
rs5994471	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs5994472	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs5994473	1.00[JPT][hapmap];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs5998234	0.87[GIH][hapmap];1.00[JPT][hapmap];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs5998249	1.00[JPT][hapmap];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs5998264	0.86[ASN][1000 genomes]
rs8138116	1.00[JPT][hapmap];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8142970	1.00[JPT][hapmap]
rs9606897	1.00[JPT][hapmap]
rs9606899	1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs9606900	1.00[JPT][hapmap]
rs9606901	1.00[ASN][1000 genomes]
rs9606909	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9606910	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9606911	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9609397	1.00[CHD][hapmap];1.00[JPT][hapmap]
rs9609413	1.00[JPT][hapmap]
rs9609421	1.00[CHD][hapmap];0.86[GIH][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs9609422	0.97[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs9609424	0.89[AFR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9609434	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9609435	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9609438	1.00[ASN][1000 genomes]
rs9609440	1.00[ASN][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	nsv1060529	chr22:32370432-32525699	Flanking Active TSS Active TSS Enhancers Weak transcription Genic enhancers Strong transcription Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	32 gene(s)	inside rSNPs	diseases
2	nsv834177	chr22:32416679-32594663	Flanking Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	37 gene(s)	inside rSNPs	diseases
3	esv1803811	chr22:32441022-32509431	Enhancers Flanking Active TSS Weak transcription Strong transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
4	nsv948789	chr22:32462505-32764760	Enhancers Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Active TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases
5	nsv1065175	chr22:32467617-32761093	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases
6	nsv544680	chr22:32467617-32761093	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	43 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	chr22:32468400-32476600	Enhancers	Fetal Intestine Large	intestine
2	chr22:32469400-32489800	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr22:32469600-32478200	Genic enhancers	Fetal Intestine Small	intestine
4	chr22:32472600-32479200	Weak transcription	Right Ventricle	heart
5	chr22:32473400-32495000	Weak transcription	Colonic Mucosa	Colon
6	chr22:32473600-32495600	Weak transcription	Rectal Mucosa Donor 31	rectum
7	chr22:32474600-32476600	Enhancers	Liver	Liver
8	chr22:32475400-32478000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
9	chr22:32475600-32476600	Enhancers	Duodenum Mucosa	Duodenum
10	chr22:32475600-32476800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr22:32476000-32476600	Enhancers	Gastric	stomach
12	chr22:32476000-32476600	Enhancers	Pancreas	Pancrea
13	chr22:32476200-32477200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
14	chr22:32476200-32478200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
15	chr22:32476200-32495800	Weak transcription	Stomach Mucosa	stomach
16	chr22:32476400-32477400	Weak transcription	Left Ventricle	heart
17	chr22:32476400-32481600	Weak transcription	Fetal Heart	heart
18	chr22:32476600-32477600	Weak transcription	Duodenum Mucosa	Duodenum
19	chr22:32476600-32479800	Weak transcription	Liver	Liver
20	chr22:32476600-32480400	Weak transcription	Fetal Intestine Large	intestine
21	chr22:32476600-32499400	Weak transcription	Pancreas	Pancrea

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