Variant report

Variant	rs12174209
Chromosome Location	chr6:145207461-145207462
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	chr6:145199350..145203488-chr6:145205369..145208032,3	K562	blood:
2	chr6:145201257..145203488-chr6:145205369..145207840,2	K562	blood:

Extended variants
information (count: 40 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:36)

rs_ID	r²[population]
rs11969748	0.86[EUR][1000 genomes]
rs13210332	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs4323328	0.85[EUR][1000 genomes]
rs4487599	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs57337295	0.85[EUR][1000 genomes]
rs6570656	0.84[EUR][1000 genomes]
rs6913165	0.86[EUR][1000 genomes]
rs71547172	0.91[AMR][1000 genomes]
rs7769065	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs9285505	0.87[EUR][1000 genomes]
rs9322003	0.87[EUR][1000 genomes]
rs9322004	0.87[EUR][1000 genomes]
rs9322005	0.86[EUR][1000 genomes]
rs9373433	0.86[EUR][1000 genomes]
rs9373434	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs9376869	0.87[EUR][1000 genomes]
rs9376874	0.86[EUR][1000 genomes]
rs9386089	0.86[EUR][1000 genomes]
rs9390243	0.92[AFR][1000 genomes];0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs9390251	0.86[EUR][1000 genomes]
rs9390252	0.86[EUR][1000 genomes]
rs9390253	0.86[EUR][1000 genomes]
rs9390254	0.83[EUR][1000 genomes]
rs9390257	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs9399514	0.85[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs9399519	0.85[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs9399520	0.86[EUR][1000 genomes]
rs9403621	0.95[AFR][1000 genomes];0.94[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs9403627	0.87[EUR][1000 genomes]
rs9403628	0.94[AMR][1000 genomes];0.87[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs9403629	0.86[EUR][1000 genomes]
rs9403631	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs9403633	0.86[EUR][1000 genomes]
rs9403634	0.85[EUR][1000 genomes]
rs9497120	0.88[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs9497121	0.88[AMR][1000 genomes];0.87[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1016747	chr6:144917411-145599874	Flanking Active TSS Enhancers ZNF genes & repeats Strong transcription Weak transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
2	nsv464070	chr6:145184504-145214952	Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
3	nsv604823	chr6:145184504-145214952	Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
4	esv1850377	chr6:145199259-145319640	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	Chromatin interactive region lncRNA	4 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	chr6:145206600-145208800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr6:145206600-145208800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr6:145207000-145209400	Enhancers	K562	blood

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