Variant report

Variant	rs7533350
Chromosome Location	chr1:169869640-169869641
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr1:169866713..169870686-chr1:169874035..169877977,4	K562	blood:
2	chr1:169857692..169860981-chr1:169868132..169871394,3	K562	blood:
3	chr1:169867701..169870686-chr1:169875443..169877977,2	K562	blood:
4	chr1:169844264..169846612-chr1:169869148..169870658,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000000457	Chromatin interaction

Extended variants
information (count: 29 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs10458398	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs10800487	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs10919267	0.84[ASN][1000 genomes]
rs10919268	1.00[ASN][1000 genomes]
rs10919269	1.00[ASN][1000 genomes]
rs12023729	1.00[ASN][1000 genomes]
rs12024570	1.00[ASN][1000 genomes]
rs12025296	1.00[ASN][1000 genomes]
rs12027790	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs12035711	1.00[ASN][1000 genomes]
rs12044536	1.00[ASN][1000 genomes]
rs12066551	1.00[ASN][1000 genomes]
rs12077708	1.00[ASN][1000 genomes]
rs12083317	1.00[ASN][1000 genomes]
rs16862931	1.00[AMR][1000 genomes]
rs2103641	1.00[ASN][1000 genomes]
rs2272912	1.00[ASN][1000 genomes]
rs2272915	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs28364665	1.00[AMR][1000 genomes]
rs7531947	1.00[ASN][1000 genomes]
rs7532990	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3451367	chr1:169630075-169976964	Strong transcription Flanking Active TSS Genic enhancers Enhancers Weak transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
2	esv1814601	chr1:169782006-169885186	Weak transcription Active TSS Flanking Active TSS Enhancers Strong transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
3	esv1821503	chr1:169782006-169885186	Weak transcription Strong transcription Genic enhancers Flanking Active TSS Enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
4	esv1847722	chr1:169782006-169885186	Strong transcription Weak transcription ZNF genes & repeats Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
5	esv2757760	chr1:169782006-169885186	Strong transcription Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
6	esv2758976	chr1:169782006-169885186	Strong transcription Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent/Poised TSS Enhancers Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
7	nsv428268	chr1:169782006-169885186	Strong transcription ZNF genes & repeats Weak transcription Enhancers Active TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
8	esv1845220	chr1:169782006-169933886	Strong transcription Weak transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:169868200-169869800	Enhancers	Fetal Intestine Large	intestine
2	chr1:169869000-169871600	Enhancers	Rectal Mucosa Donor 29	rectum
3	chr1:169869600-169870800	Weak transcription	Fetal Intestine Small	intestine

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