Variant report

Variant	rs6023154
Chromosome Location	chr20:52979164-52979165
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	chr17:57921876..57923469-chr20:52978562..52980794,2	MCF-7	breast:
2	chr20:52886227..52888754-chr20:52977596..52979522,2	MCF-7	breast:

Extended variants
information (count: 54 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:51)

rs_ID	r²[population]
rs1358806	0.81[ASN][1000 genomes]
rs1358807	0.81[ASN][1000 genomes]
rs1407043	0.90[ASN][1000 genomes]
rs1590206	0.80[ASN][1000 genomes]
rs16999597	0.88[ASN][1000 genomes]
rs1841860	0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1923118	0.88[ASN][1000 genomes]
rs2126676	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs28406117	0.88[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs28429972	0.95[ASN][1000 genomes]
rs2870329	0.81[ASN][1000 genomes]
rs56881371	1.00[ASN][1000 genomes]
rs59924072	0.95[ASN][1000 genomes]
rs6013987	0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6013989	0.94[ASN][1000 genomes]
rs6013997	0.90[ASN][1000 genomes]
rs6013999	0.88[ASN][1000 genomes]
rs6014003	0.88[ASN][1000 genomes]
rs6014004	0.87[ASN][1000 genomes]
rs6014005	0.88[ASN][1000 genomes]
rs6023153	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6023155	0.99[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6023156	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6023158	0.99[ASN][1000 genomes]
rs6023163	0.95[ASN][1000 genomes]
rs6023164	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6023180	0.91[ASN][1000 genomes]
rs6023183	0.81[ASN][1000 genomes]
rs6023185	0.86[ASN][1000 genomes]
rs6023189	0.89[ASN][1000 genomes]
rs6023192	0.88[ASN][1000 genomes]
rs6023193	0.88[ASN][1000 genomes]
rs6023197	0.81[ASN][1000 genomes]
rs6023203	0.88[ASN][1000 genomes]
rs6091856	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6097934	0.99[ASN][1000 genomes]
rs6097938	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6097939	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6097940	0.99[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6097941	0.99[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6097945	0.92[ASN][1000 genomes]
rs6097946	0.92[ASN][1000 genomes]
rs6097955	0.80[ASN][1000 genomes]
rs6097957	0.81[ASN][1000 genomes]
rs6097963	0.88[ASN][1000 genomes]
rs6097964	0.80[ASN][1000 genomes]
rs6097967	0.80[ASN][1000 genomes]
rs73624107	0.96[ASN][1000 genomes]
rs73624108	0.95[ASN][1000 genomes]
rs73624110	0.95[ASN][1000 genomes]
rs793033	0.81[EUR][1000 genomes];0.86[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv586224	chr20:52474850-53279490	Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Active TSS Bivalent/Poised TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	338 gene(s)	inside rSNPs	diseases
2	nsv834011	chr20:52858341-53086042	Enhancers ZNF genes & repeats Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS	Chromatin interactive region lncRNA	55 gene(s)	inside rSNPs	diseases
3	nsv834012	chr20:52921007-53097177	Flanking Active TSS Weak transcription Bivalent/Poised TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:52976600-52983400	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr20:52976600-52985200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
3	chr20:52977600-52985200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
4	chr20:52977800-52979200	Enhancers	Fetal Brain Male	brain
5	chr20:52977800-52985200	Weak transcription	HUES48 Cell Line	embryonic stem cell
6	chr20:52978200-52979600	Enhancers	Ovary	ovary
7	chr20:52978800-52979200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr20:52978800-52979200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
9	chr20:52978800-52979800	Enhancers	iPS-18 Cell Line	embryonic stem cell
10	chr20:52979000-52979200	Enhancers	Cortex derived primary cultured neurospheres	brain
11	chr20:52979000-52979200	Enhancers	Right Atrium	heart

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