Variant report

Variant	rs6851414
Chromosome Location	chr4:121885466-121885467
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 25 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs11734432	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1376104	0.95[AFR][1000 genomes]
rs1376106	0.95[AFR][1000 genomes]
rs1817036	1.00[AMR][1000 genomes]
rs1868716	1.00[AMR][1000 genomes]
rs1901137	0.95[AFR][1000 genomes]
rs2390063	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2390064	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2892921	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4257672	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4368630	1.00[AMR][1000 genomes]
rs4406042	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4422434	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4422435	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6534227	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6534228	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6825508	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6836209	0.95[AFR][1000 genomes]
rs6852202	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6852244	0.95[AFR][1000 genomes]
rs6852427	0.95[AFR][1000 genomes];1.00[AMR][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	nsv998094	chr4:121504565-122374203	Weak transcription Active TSS Enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
2	nsv1009395	chr4:121841442-122557363	Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
3	nsv537235	chr4:121841442-122557363	Enhancers Bivalent Enhancer Weak transcription Bivalent/Poised TSS ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
4	esv3386870	chr4:121867625-122208448	Weak transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:121882400-121885600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr4:121884600-121887400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
3	chr4:121884600-121887600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr4:121884800-121887200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr4:121885400-121887400	Enhancers	HUES64 Cell Line	embryonic stem cell

Quick Search:

Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

what's new

Quick links