Variant report

Variant	rs6426114
Chromosome Location	chr1:224533262-224533263
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	chr1:224532645..224534213-chr1:224544548..224547414,2	MCF-7	breast:
2	chr1:224530838..224534137-chr1:224542952..224546096,3	K562	blood:

Variant related genes	Relation type
ENSG00000143771	Chromatin interaction

Extended variants
information (count: 94 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:91)

rs_ID	r²[population]
rs10158063	0.81[ASN][1000 genomes]
rs10733024	0.88[ASN][1000 genomes]
rs10737442	0.93[ASN][1000 genomes]
rs10737443	0.93[AFR][1000 genomes];0.94[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs10753462	0.82[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs10753464	0.93[AFR][1000 genomes];0.88[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs10799562	0.93[ASN][1000 genomes]
rs10799563	0.82[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs10799566	0.95[ASN][1000 genomes]
rs10799567	0.93[AFR][1000 genomes];0.82[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs10799568	0.93[ASN][1000 genomes]
rs10916585	0.82[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs11802486	0.84[ASN][1000 genomes]
rs11811730	0.91[ASN][1000 genomes]
rs16846031	0.88[ASN][1000 genomes]
rs16846094	0.93[ASN][1000 genomes]
rs16846214	0.93[ASN][1000 genomes]
rs16846244	0.93[ASN][1000 genomes]
rs1806742	0.86[ASN][1000 genomes]
rs2001712	0.93[ASN][1000 genomes]
rs2404783	0.93[ASN][1000 genomes]
rs2404856	0.91[ASN][1000 genomes]
rs2404857	0.89[ASN][1000 genomes]
rs2404858	0.82[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs2404859	0.93[ASN][1000 genomes]
rs2404861	0.82[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs2405062	0.84[ASN][1000 genomes]
rs2405065	0.95[ASN][1000 genomes]
rs2405067	0.87[AFR][1000 genomes];0.94[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs2405070	0.91[ASN][1000 genomes]
rs2896990	0.93[ASN][1000 genomes]
rs2896992	0.82[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs2897054	0.84[ASN][1000 genomes]
rs3754090	0.93[ASN][1000 genomes]
rs3767721	0.89[ASN][1000 genomes]
rs3767722	0.93[ASN][1000 genomes]
rs3767723	0.93[ASN][1000 genomes]
rs3767724	0.93[ASN][1000 genomes]
rs3767725	0.93[ASN][1000 genomes]
rs4146965	0.93[ASN][1000 genomes]
rs4146966	0.93[ASN][1000 genomes]
rs4233234	0.93[ASN][1000 genomes]
rs4256779	0.95[ASN][1000 genomes]
rs4420060	0.84[ASN][1000 genomes]
rs4457542	0.95[ASN][1000 genomes]
rs4628473	0.95[ASN][1000 genomes]
rs4653575	0.93[ASN][1000 genomes]
rs4653579	0.82[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs4653580	0.82[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs4653581	0.93[ASN][1000 genomes]
rs4653583	0.95[ASN][1000 genomes]
rs4653584	0.93[AFR][1000 genomes];0.82[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs4654011	0.81[ASN][1000 genomes]
rs4654017	0.88[ASN][1000 genomes]
rs4654019	0.93[ASN][1000 genomes]
rs4654022	0.93[ASN][1000 genomes]
rs4654023	0.93[ASN][1000 genomes]
rs4654032	0.95[ASN][1000 genomes]
rs4654033	0.93[AFR][1000 genomes];0.82[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs4654034	0.93[AFR][1000 genomes];0.82[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs55675086	0.88[ASN][1000 genomes]
rs55980628	0.93[ASN][1000 genomes]
rs57324770	0.88[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs58855990	0.93[ASN][1000 genomes]
rs59106681	0.95[ASN][1000 genomes]
rs6426088	0.84[ASN][1000 genomes]
rs6426094	0.88[ASN][1000 genomes]
rs6426110	0.82[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs6426115	0.95[ASN][1000 genomes]
rs6426117	0.93[ASN][1000 genomes]
rs6681790	0.95[ASN][1000 genomes]
rs6682667	0.84[ASN][1000 genomes]
rs6685600	0.88[AFR][1000 genomes];0.82[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs6691689	0.93[ASN][1000 genomes]
rs6694745	0.93[ASN][1000 genomes]
rs6696795	0.93[ASN][1000 genomes]
rs6699017	0.88[ASN][1000 genomes]
rs73118046	0.88[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs73128468	0.88[ASN][1000 genomes]
rs73130436	0.93[ASN][1000 genomes]
rs73130448	0.93[ASN][1000 genomes]
rs73130455	0.93[ASN][1000 genomes]
rs73130462	0.93[ASN][1000 genomes]
rs73130464	0.93[ASN][1000 genomes]
rs7521015	0.84[ASN][1000 genomes]
rs7522392	0.88[ASN][1000 genomes]
rs7529143	0.82[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs7530205	0.93[ASN][1000 genomes]
rs7534101	0.95[ASN][1000 genomes]
rs7534447	0.93[ASN][1000 genomes]
rs9287027	0.84[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	nsv8868	chr1:224383023-224752531	Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent/Poised TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
2	nsv469889	chr1:224440354-224634374	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
3	nsv482318	chr1:224440354-224634374	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	21 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:224529200-224544000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr1:224531800-224535400	Weak transcription	Primary T killer memory cells from peripheral blood	blood

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