Variant report

Variant	rs12891714
Chromosome Location	chr14:84859965-84859966
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 30 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs10131053	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10131334	0.83[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs10144393	0.87[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs12431750	0.83[AFR][1000 genomes];0.82[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs12432589	0.98[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12879664	0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12880194	0.81[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs4243672	0.91[AFR][1000 genomes];0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4259973	0.80[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs4328366	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4350506	0.82[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs4386065	0.97[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4410004	0.95[ASN][1000 genomes]
rs4418993	0.81[AFR][1000 genomes]
rs4489939	0.95[ASN][1000 genomes]
rs4500652	0.88[ASN][1000 genomes]
rs4904174	0.81[EUR][1000 genomes]
rs55682233	0.91[ASN][1000 genomes]
rs61984240	0.88[AFR][1000 genomes];0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7148496	0.95[ASN][1000 genomes]
rs7148700	0.84[AFR][1000 genomes];0.96[ASN][1000 genomes]
rs7151303	0.92[ASN][1000 genomes]
rs7158947	0.90[AFR][1000 genomes];0.81[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs7160613	0.87[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs71908900	0.94[ASN][1000 genomes]
rs8003576	0.93[ASN][1000 genomes]
rs8008906	0.81[EUR][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	nsv832845	chr14:84726378-84900199	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
2	esv2751288	chr14:84815330-85704047	Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS Active TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv85151	chr14:84858000-84860441	Weak transcription	n/a	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:84856400-84864400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links