Variant report

Variant	rs2514172
Chromosome Location	chr11:83695908-83695909
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 42 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:38)

rs_ID	r²[population]
rs10792700	0.95[ASN][1000 genomes]
rs1384749	0.88[ASN][1000 genomes]
rs1384757	0.83[ASN][1000 genomes]
rs1384758	0.86[ASN][1000 genomes]
rs1483411	0.92[ASN][1000 genomes]
rs1545863	0.90[ASN][1000 genomes]
rs1545864	0.93[ASN][1000 genomes]
rs1601091	0.87[ASN][1000 genomes]
rs1601093	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1945817	0.81[AMR][1000 genomes]
rs1982733	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2200204	0.93[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs2374466	0.92[ASN][1000 genomes]
rs2449584	0.85[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs2449589	0.81[ASN][1000 genomes]
rs2449590	0.81[ASN][1000 genomes]
rs2449593	0.92[ASN][1000 genomes]
rs2449595	0.91[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs2449596	0.94[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs2449597	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2449599	0.84[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs2449600	0.95[AMR][1000 genomes];0.86[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2514143	0.91[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs2514145	0.94[ASN][1000 genomes]
rs2514147	0.94[ASN][1000 genomes]
rs2514148	0.94[ASN][1000 genomes]
rs2514149	0.95[ASN][1000 genomes]
rs2514150	0.93[ASN][1000 genomes]
rs2514151	0.93[ASN][1000 genomes]
rs2514152	0.84[ASN][1000 genomes]
rs2514159	0.84[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs2514160	0.92[ASN][1000 genomes]
rs2514161	0.82[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs2514162	0.92[ASN][1000 genomes]
rs2514168	0.81[EUR][1000 genomes]
rs7107725	0.88[ASN][1000 genomes]
rs7934123	0.81[ASN][1000 genomes]
rs960532	0.93[ASN][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	nsv898025	chr11:83658909-83796678	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	n/a
2	nsv1039924	chr11:83662904-83993497	Enhancers Active TSS Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
3	nsv541102	chr11:83662904-83993497	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
4	nsv898026	chr11:83685801-83789540	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:83691600-83701200	Weak transcription	Brain Hippocampus Middle	brain

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links