Variant report

Variant	rs67733453
Chromosome Location	chr7:19729631-19729632
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	chr7:19727945..19730939-chr7:19734576..19737484,2	MCF-7	breast:

Extended variants
information (count: 26 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs12532153	0.84[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12536065	0.87[AMR][1000 genomes]
rs12667746	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs3735617	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4591920	0.86[AMR][1000 genomes]
rs4620176	0.83[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs59113291	0.83[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs61223965	0.90[EUR][1000 genomes]
rs67120244	0.87[AMR][1000 genomes]
rs67568939	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6962595	0.80[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs72591424	0.93[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs72591425	0.83[ASN][1000 genomes]
rs72591428	0.80[ASN][1000 genomes]
rs73274010	0.84[AFR][1000 genomes]
rs73274011	0.84[AFR][1000 genomes]
rs73274017	0.84[AFR][1000 genomes]
rs73274019	0.84[AFR][1000 genomes]
rs7803245	0.83[ASN][1000 genomes]
rs9690344	0.84[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs992934	0.86[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1018601	chr7:19272360-20008881	Enhancers Transcr. at gene 5' and 3' Weak transcription Strong transcription Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	24 gene(s)	inside rSNPs	diseases
2	nsv1020275	chr7:19677535-19730557	Enhancers Active TSS Weak transcription Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
3	nsv1033223	chr7:19682192-20461375	Enhancers Active TSS Flanking Active TSS Strong transcription Weak transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
4	nsv538795	chr7:19682192-20461375	Weak transcription Enhancers Active TSS Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
5	nsv524807	chr7:19714156-19803925	Enhancers Strong transcription Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region miRNA	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:19728800-19731400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr7:19729000-19729800	Enhancers	K562	blood
3	chr7:19729200-19729800	Enhancers	ES-I3 Cell Line	embryonic stem cell
4	chr7:19729200-19729800	Enhancers	iPS-15b Cell Line	embryonic stem cell
5	chr7:19729200-19730000	Enhancers	H9 Cell Line	embryonic stem cell
6	chr7:19729400-19737000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
7	chr7:19729400-19739800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
8	chr7:19729600-19736000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links