Variant report

Variant	rs60790450
Chromosome Location	chr7:71497456-71497457
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 36 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:28)

rs_ID	r²[population]
rs10251758	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10277893	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1034806	0.82[EUR][1000 genomes]
rs1099452	0.82[EUR][1000 genomes]
rs1525129	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1525130	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17349645	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17428098	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17428133	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2867564	0.82[EUR][1000 genomes]
rs2867565	0.82[EUR][1000 genomes]
rs35720869	0.82[EUR][1000 genomes]
rs4469348	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57300068	0.82[ASN][1000 genomes]
rs6980132	0.82[EUR][1000 genomes]
rs73368146	0.80[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73368155	0.80[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7790072	1.00[ASN][1000 genomes]
rs844691	0.82[EUR][1000 genomes]
rs844692	0.82[EUR][1000 genomes]
rs844693	0.82[EUR][1000 genomes]
rs844694	0.82[EUR][1000 genomes]
rs844695	0.82[EUR][1000 genomes]
rs844696	0.82[EUR][1000 genomes]
rs844699	0.82[EUR][1000 genomes]
rs844702	0.82[EUR][1000 genomes]
rs844734	0.82[EUR][1000 genomes]
rs844736	0.82[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	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
6	nsv831023	chr7:71443549-71588033	Enhancers Strong transcription Weak transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
7	nsv531373	chr7:71487076-71765613	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
8	nsv817506	chr7:71488542-71935721	Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription Bivalent/Poised TSS ZNF genes & repeats Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:71484600-71498400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr7:71490800-71498400	Weak transcription	Brain Anterior Caudate	brain
3	chr7:71490800-71498400	Weak transcription	Brain Substantia Nigra	brain
4	chr7:71493400-71503600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr7:71493600-71497600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
6	chr7:71493600-71498400	Weak transcription	Thymus	Thymus
7	chr7:71494400-71497800	Weak transcription	Fetal Brain Male	brain
8	chr7:71495000-71497600	Weak transcription	Fetal Thymus	thymus
9	chr7:71495200-71497800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
10	chr7:71495400-71497800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
11	chr7:71495400-71502400	Weak transcription	Primary hematopoietic stem cells	blood
12	chr7:71495800-71497800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr7:71496600-71497800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
14	chr7:71497200-71499000	Enhancers	Fetal Heart	heart
15	chr7:71497400-71497600	Enhancers	Left Ventricle	heart
16	chr7:71497400-71498400	Enhancers	Brain Hippocampus Middle	brain
17	chr7:71497400-71499000	Enhancers	Dnd41	blood

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