Variant report

Variant	rs17108027
Chromosome Location	chr14:79118985-79118986
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	chr14:79117364..79120098-chr14:79128016..79129818,2	K562	blood:

Extended variants
information (count: 39 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10483908	0.94[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.89[MEX][hapmap];0.89[TSI][hapmap];0.80[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10483911	0.85[TSI][hapmap]
rs10483912	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs12587427	0.89[ASN][1000 genomes]
rs17107907	0.94[CHB][hapmap];1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs17107912	0.94[CHB][hapmap];0.95[CHD][hapmap];1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs17107930	1.00[CHB][hapmap];1.00[JPT][hapmap];0.80[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs17107978	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs17107986	0.94[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs17107993	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs17107998	0.85[TSI][hapmap]
rs17108011	0.94[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs17108021	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs17108040	1.00[CHB][hapmap];0.95[CHD][hapmap];1.00[JPT][hapmap]
rs17835493	1.00[CEU][hapmap];0.89[EUR][1000 genomes]
rs2287495	0.94[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs55853427	0.82[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs57416351	0.80[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs58271165	0.89[ASN][1000 genomes]
rs59887424	0.97[ASN][1000 genomes]
rs60568650	0.90[ASN][1000 genomes]
rs61393149	0.80[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs61976092	0.80[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs61976120	0.84[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs61976143	0.89[EUR][1000 genomes]
rs61976144	0.89[EUR][1000 genomes]
rs61976145	0.87[EUR][1000 genomes]
rs6574456	0.94[CHB][hapmap];1.00[JPT][hapmap];0.80[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6574459	0.93[ASN][1000 genomes]
rs7142533	1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs7153070	1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs72683573	0.89[EUR][1000 genomes]
rs74064325	0.87[ASN][1000 genomes]
rs8017659	0.80[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs8019422	1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9646166	0.83[CHD][hapmap];1.00[JPT][hapmap];0.97[LWK][hapmap];0.84[MKK][hapmap];0.90[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	esv2760000	chr14:78875607-79173528	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	esv2758363	chr14:78903610-79173528	Enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	esv2757578	chr14:79055398-79140536	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:79108200-79123600	Weak transcription	Brain Germinal Matrix	brain
2	chr14:79111400-79123200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
3	chr14:79115800-79119200	Weak transcription	Cortex derived primary cultured neurospheres	brain

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links