Variant report

Variant	rs2403091
Chromosome Location	chr12:83600760-83600761
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 38 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs10746271	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10778949	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10862604	0.92[AMR][1000 genomes];0.89[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs10862605	0.92[AMR][1000 genomes];0.89[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs11115641	0.92[AMR][1000 genomes];0.89[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs1356441	0.85[EUR][1000 genomes]
rs1356442	0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1517814	0.85[EUR][1000 genomes]
rs2037258	0.92[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs2037259	0.92[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs2037260	0.92[AMR][1000 genomes];0.89[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs2403092	0.94[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs2403093	0.95[AMR][1000 genomes];0.89[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs2896455	0.95[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs4242871	0.92[AMR][1000 genomes];0.89[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs4882555	0.85[EUR][1000 genomes]
rs4882556	0.90[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs4882557	0.84[EUR][1000 genomes]
rs6539708	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6539709	0.91[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs6539711	0.92[AMR][1000 genomes];0.89[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs6539713	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs71445206	0.87[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs7301011	0.92[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7302888	0.90[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs7313122	0.80[AMR][1000 genomes]
rs7316717	0.92[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7953127	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7962167	0.89[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs7962962	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7964401	0.91[AMR][1000 genomes]
rs7973484	0.92[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7979811	0.87[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs970483	0.85[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	nsv521849	chr12:83013783-83991479	Weak transcription ZNF genes & repeats Enhancers Strong transcription Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
2	nsv559559	chr12:83505512-83765069	ZNF genes & repeats Enhancers Flanking Active TSS Weak transcription Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv899352	chr12:83556258-83671428	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	n/a
4	nsv559560	chr12:83599202-83608767	Flanking Active TSS Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:83594600-83604200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr12:83596600-83604200	Weak transcription	H1 Cell Line	embryonic stem cell
3	chr12:83597000-83604200	Weak transcription	iPS-18 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links