Variant report

Variant	rs17827974
Chromosome Location	chr4:55503813-55503814
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	chr4:55503201..55504980-chr4:55510390..55512353,2	K562	blood:
2	chr4:55502404..55505387-chr4:55506992..55509953,2	MCF-7	breast:

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

rSNPs within LD-proxies of this variant (count:35)

rs_ID	r²[population]
rs1005438	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs11730497	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs11733357	0.87[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs11736016	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs12498193	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs12504244	0.81[AFR][1000 genomes];0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs12512899	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs13128858	0.84[EUR][1000 genomes]
rs13138563	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs2215726	0.83[AFR][1000 genomes];0.87[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs2237031	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs2237035	0.87[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs2282778	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs2282779	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs2282780	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs2282781	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs2703456	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs34284864	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs35441406	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs3756197	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs3819387	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs3819389	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs3819392	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs3822213	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4864915	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs6554196	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs6825657	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs71599647	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs759082	0.85[AFR][1000 genomes];0.87[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs759083	0.84[EUR][1000 genomes]
rs7655556	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs7655588	0.88[AFR][1000 genomes];0.86[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs7656858	0.88[AFR][1000 genomes];0.87[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs7675203	0.85[AFR][1000 genomes];0.87[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs7697799	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1008793	chr4:55060925-55535807	Enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
2	nsv537098	chr4:55060925-55535807	Enhancers Active TSS Genic enhancers Flanking Active TSS Bivalent/Poised TSS Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
3	nsv999400	chr4:55143598-55776995	Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
4	nsv997430	chr4:55253397-55529288	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
5	esv3367952	chr4:55437113-55724644	Bivalent/Poised TSS Strong transcription Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
6	nsv1004488	chr4:55440944-55511101	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
7	nsv1009708	chr4:55440944-55513275	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
8	nsv1010702	chr4:55440944-55528450	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
9	nsv1003671	chr4:55445652-55513275	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
10	nsv1001906	chr4:55447189-55505721	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
11	nsv537100	chr4:55447189-55505721	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
12	nsv521933	chr4:55449616-55512066	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS	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	chr4:55501800-55506600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr4:55501800-55506600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr4:55503600-55504000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links