Variant report

Variant	rs4719197
Chromosome Location	chr7:71430789-71430790
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:71430764..71432829-chr7:71445344..71447656,2	K562	blood:

Extended variants
information (count: 47 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:39)

rs_ID	r²[population]
rs10251758	0.94[EUR][1000 genomes]
rs10258507	0.87[CEU][hapmap];0.80[EUR][1000 genomes]
rs10277893	0.94[EUR][1000 genomes]
rs1034806	0.94[EUR][1000 genomes]
rs1099451	0.87[CEU][hapmap];0.83[EUR][1000 genomes]
rs1099452	0.94[EUR][1000 genomes]
rs1525129	1.00[JPT][hapmap];0.85[EUR][1000 genomes]
rs1525130	0.85[EUR][1000 genomes]
rs17137604	0.87[CEU][hapmap]
rs17137608	0.87[CEU][hapmap]
rs17144164	0.87[CEU][hapmap]
rs17349645	1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[EUR][1000 genomes]
rs17428098	1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[EUR][1000 genomes]
rs17428133	1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[EUR][1000 genomes]
rs2867564	0.87[CEU][hapmap];0.94[EUR][1000 genomes]
rs2867565	0.94[EUR][1000 genomes]
rs35720869	0.94[EUR][1000 genomes]
rs4469348	0.84[EUR][1000 genomes]
rs57300068	0.89[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs59937976	0.80[EUR][1000 genomes]
rs6963963	0.80[EUR][1000 genomes]
rs6968406	0.80[EUR][1000 genomes]
rs6980132	0.87[CEU][hapmap];0.94[EUR][1000 genomes]
rs73368146	0.85[EUR][1000 genomes]
rs73368155	0.85[EUR][1000 genomes]
rs7790072	0.87[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[EUR][1000 genomes]
rs844691	0.94[EUR][1000 genomes]
rs844692	0.87[CEU][hapmap];0.94[EUR][1000 genomes]
rs844693	0.87[CEU][hapmap];0.94[EUR][1000 genomes]
rs844694	0.87[CEU][hapmap];0.94[EUR][1000 genomes]
rs844695	0.94[EUR][1000 genomes]
rs844696	0.94[EUR][1000 genomes]
rs844698	0.89[EUR][1000 genomes]
rs844699	0.87[CEU][hapmap];0.94[EUR][1000 genomes]
rs844702	0.94[EUR][1000 genomes]
rs844734	0.94[EUR][1000 genomes]
rs844735	0.88[EUR][1000 genomes]
rs844736	0.94[EUR][1000 genomes]
rs844740	0.90[EUR][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	nsv1026896	chr7:71003462-71721516	Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv1027496	chr7:71162362-71575116	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv916220	chr7:71200006-71708048	Strong transcription Flanking Active TSS ZNF genes & repeats Enhancers Weak transcription Genic enhancers Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv531372	chr7:71300090-71909517	Enhancers Active TSS Flanking Active TSS Weak transcription Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases
5	nsv1017367	chr7:71339782-71476575	ZNF genes & repeats Active TSS Strong transcription Weak transcription Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
6	nsv888344	chr7:71406392-71488833	ZNF genes & repeats Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
7	nsv888345	chr7:71408360-71485245	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
8	nsv491610	chr7:71422560-71803630	Enhancers Weak transcription Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:71401200-71431000	Weak transcription	Primary hematopoietic stem cells	blood
2	chr7:71403400-71431000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chr7:71408000-71430800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr7:71409400-71430800	Weak transcription	Fetal Thymus	thymus
5	chr7:71424000-71430800	Weak transcription	Thymus	Thymus
6	chr7:71429400-71433000	Weak transcription	Fetal Brain Female	brain

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