Variant report

Variant	rs17011845
Chromosome Location	chr4:87297865-87297866
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 26 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs17011682	1.00[ASW][hapmap];1.00[MKK][hapmap];0.82[AFR][1000 genomes]
rs17011708	0.94[AFR][1000 genomes]
rs17011764	0.94[AFR][1000 genomes]
rs17011766	0.94[AFR][1000 genomes]
rs17011767	0.94[AFR][1000 genomes]
rs17011774	0.94[AFR][1000 genomes]
rs17011806	0.94[AFR][1000 genomes]
rs17011815	1.00[ASW][hapmap];0.87[LWK][hapmap];1.00[MKK][hapmap];0.83[AFR][1000 genomes]
rs17011819	0.94[AFR][1000 genomes]
rs17011853	1.00[ASW][hapmap];0.87[LWK][hapmap];1.00[MKK][hapmap];1.00[AFR][1000 genomes]
rs17011858	0.89[AFR][1000 genomes]
rs17011872	1.00[AFR][1000 genomes]
rs2001612	0.88[AFR][1000 genomes]
rs4283624	0.82[AFR][1000 genomes]
rs6844636	0.82[AFR][1000 genomes]
rs6844802	0.82[AFR][1000 genomes]
rs7661679	0.94[AFR][1000 genomes]
rs7667204	0.94[AFR][1000 genomes]
rs7675381	0.94[AFR][1000 genomes]
rs7691277	1.00[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv594786	chr4:87076360-87609320	Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	7 gene(s)	inside rSNPs	diseases
2	nsv999470	chr4:87165663-87514552	Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	6 gene(s)	inside rSNPs	diseases
3	nsv537164	chr4:87165663-87514552	Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	6 gene(s)	inside rSNPs	diseases
4	nsv934210	chr4:87197339-87325578	Weak transcription Flanking Active TSS Strong transcription Enhancers ZNF genes & repeats Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	nsv594787	chr4:87221827-87888667	Enhancers Weak transcription Strong transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
6	nsv1012836	chr4:87279206-87643558	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	6 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	chr4:87275600-87302400	Weak transcription	Aorta	Aorta
2	chr4:87281600-87315800	Weak transcription	Stomach Smooth Muscle	stomach
3	chr4:87290400-87308200	Weak transcription	Ovary	ovary
4	chr4:87297400-87298000	Enhancers	Pancreatic Islets	Pancreatic Islet
5	chr4:87297600-87298400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr4:87297600-87298800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links