Variant report

Variant	rs73711226
Chromosome Location	chr7:84448703-84448704
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr7:84443133..84444638-chr7:84447039..84448903,2	MCF-7	breast:
2	chr7:84437053..84440861-chr7:84448481..84451648,4	K562	blood:
3	chr7:84438468..84441991-chr7:84448481..84451648,3	K562	blood:

Extended variants
information (count: 41 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs56308636	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs58138808	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs58925383	1.00[AMR][1000 genomes]
rs59348422	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59657041	1.00[AMR][1000 genomes]
rs60691164	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61463589	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73711260	1.00[AMR][1000 genomes]
rs73711608	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73711610	1.00[AMR][1000 genomes]
rs73711612	1.00[AMR][1000 genomes]
rs73711613	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73711614	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73711617	1.00[AMR][1000 genomes]
rs73711623	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73711626	1.00[AMR][1000 genomes]
rs73711630	1.00[AMR][1000 genomes]
rs73712829	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73712831	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73712836	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73712837	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73712839	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73712853	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73712858	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73712859	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73712862	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73713538	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73713540	1.00[AMR][1000 genomes]
rs73713545	1.00[AMR][1000 genomes]
rs73713546	1.00[AMR][1000 genomes]
rs73713548	1.00[AMR][1000 genomes]
rs73713549	1.00[AMR][1000 genomes]
rs73713555	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73713913	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv529344	chr7:83714286-84592857	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
2	nsv949446	chr7:84003501-84763823	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
3	nsv888641	chr7:84168615-84453100	Enhancers Active TSS Flanking Active TSS Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
4	nsv888643	chr7:84196258-84453100	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv831049	chr7:84277599-84475710	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
6	esv34238	chr7:84279023-84591966	Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
7	nsv831050	chr7:84355996-84527261	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	2 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	chr7:84439600-84450000	Weak transcription	K562	blood
2	chr7:84448400-84448800	Enhancers	Colon Smooth Muscle	Colon
3	chr7:84448400-84450200	Enhancers	Fetal Heart	heart

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