Variant report

Variant	rs60920648
Chromosome Location	chr14:96939108-96939109
allele	C/G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 43 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10136266	0.90[EUR][1000 genomes]
rs10136277	0.88[EUR][1000 genomes]
rs10139164	0.92[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10140247	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10143834	0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10144704	0.84[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10467873	0.82[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11160341	0.91[EUR][1000 genomes]
rs11160344	0.90[EUR][1000 genomes]
rs11621566	0.80[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11621778	0.91[EUR][1000 genomes]
rs11623142	0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11625090	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11627288	0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11848720	0.87[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11848778	0.86[EUR][1000 genomes]
rs12147439	0.86[EUR][1000 genomes]
rs13329034	0.91[EUR][1000 genomes]
rs13379390	0.91[EUR][1000 genomes]
rs1484251	0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs17094149	0.92[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2274795	0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs28718054	0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs28738720	0.88[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2887550	0.91[EUR][1000 genomes]
rs4514608	0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs56184178	0.86[EUR][1000 genomes]
rs58112821	0.86[EUR][1000 genomes]
rs61435932	0.85[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs61570427	0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs66881740	0.87[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7142806	0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7146883	0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7160148	0.82[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs8013517	0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs965950	0.90[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1043142	chr14:96096263-96978016	Flanking Active TSS Weak transcription Strong transcription Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	75 gene(s)	inside rSNPs	diseases
2	nsv542177	chr14:96096263-96978016	Enhancers Bivalent Enhancer Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	75 gene(s)	inside rSNPs	diseases
3	nsv482589	chr14:96805418-96985830	Flanking Active TSS Active TSS Enhancers Weak transcription Genic enhancers Strong transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	50 gene(s)	inside rSNPs	diseases
4	nsv1042409	chr14:96832303-97115668	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Strong transcription Bivalent/Poised TSS Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
5	nsv542178	chr14:96832303-97115668	Active TSS Enhancers Strong transcription Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
6	nsv902211	chr14:96864309-96986153	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	42 gene(s)	inside rSNPs	diseases
7	esv3442210	chr14:96878392-97038700	Weak transcription Flanking Active TSS Strong transcription Enhancers Genic enhancers Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:96917200-96954800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
2	chr14:96929400-96946200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr14:96929600-96941600	Weak transcription	Pancreas	Pancrea
4	chr14:96935600-96940000	Weak transcription	Fetal Intestine Large	intestine
5	chr14:96937200-96940000	Weak transcription	Stomach Mucosa	stomach
6	chr14:96937200-96940000	Weak transcription	HepG2	liver

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links