Variant report

Variant	rs16830435
Chromosome Location	chr2:152755598-152755599
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr2:152754569..152757079-chr2:152758083..152760344,2	K562	blood:
2	chr2:152754365..152757186-chr2:152760539..152762357,2	K562	blood:
3	chr2:152754365..152757186-chr2:152760539..152763045,3	K562	blood:

Extended variants
information (count: 29 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs10930837	1.00[CEU][hapmap];0.84[CHD][hapmap];1.00[GIH][hapmap];0.93[MEX][hapmap]
rs12463883	1.00[CEU][hapmap]
rs12469117	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1356732	1.00[CEU][hapmap];0.84[CHD][hapmap];1.00[GIH][hapmap];0.93[MEX][hapmap]
rs1474172	1.00[CEU][hapmap]
rs1519710	1.00[CEU][hapmap];0.83[EUR][1000 genomes]
rs16830434	1.00[CEU][hapmap];0.91[CHB][hapmap];0.83[YRI][hapmap];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs16830450	1.00[CEU][hapmap];0.84[CHD][hapmap];1.00[GIH][hapmap];0.87[MEX][hapmap];0.85[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs16830539	1.00[CEU][hapmap]
rs3754532	1.00[CEU][hapmap];1.00[CHB][hapmap];0.90[JPT][hapmap];0.86[YRI][hapmap];0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs3820703	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4496331	1.00[CEU][hapmap]
rs4563220	1.00[CEU][hapmap];0.83[GIH][hapmap]
rs66900149	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6730903	1.00[CEU][hapmap]
rs67572576	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7562260	1.00[CEU][hapmap]
rs7580901	1.00[CEU][hapmap];0.83[EUR][1000 genomes]
rs7581344	1.00[CEU][hapmap]
rs7597915	1.00[CEU][hapmap];1.00[GIH][hapmap];0.80[MEX][hapmap]
rs883157	1.00[CEU][hapmap]
rs883170	1.00[CEU][hapmap]
rs952339	1.00[CEU][hapmap]

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	nsv1005746	chr2:152361972-153059840	Strong transcription Weak transcription Bivalent/Poised TSS Enhancers Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
2	nsv535984	chr2:152361972-153059840	Active TSS Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
3	esv3693431	chr2:152683731-152981827	Enhancers Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
4	nsv875287	chr2:152714680-153110573	Enhancers Strong transcription Weak transcription Active TSS Genic enhancers Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
5	nsv875288	chr2:152716628-153183646	Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Flanking Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
6	nsv875289	chr2:152720030-153183646	Enhancers Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Strong transcription Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:152748800-152756800	Weak transcription	Brain Angular Gyrus	brain
2	chr2:152749400-152764400	Weak transcription	Aorta	Aorta
3	chr2:152752000-152756200	Weak transcription	Fetal Brain Male	brain
4	chr2:152752000-152756800	Weak transcription	Fetal Lung	lung
5	chr2:152752000-152762400	Weak transcription	HepG2	liver
6	chr2:152753200-152756800	Weak transcription	Lung	lung
7	chr2:152753200-152763000	Weak transcription	Right Atrium	heart
8	chr2:152753200-152764800	Weak transcription	Left Ventricle	heart
9	chr2:152753600-152761200	Weak transcription	Skeletal Muscle Male	skeletal muscle
10	chr2:152755000-152756400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr2:152755000-152756600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
12	chr2:152755400-152755600	Enhancers	Brain Inferior Temporal Lobe	brain
13	chr2:152755400-152755800	Enhancers	Adipose Nuclei	Adipose
14	chr2:152755400-152756200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr2:152755400-152756800	Enhancers	Brain Hippocampus Middle	brain
16	chr2:152755400-152757200	Enhancers	Primary monocytes fromperipheralblood	blood
17	chr2:152755400-152757200	Enhancers	Monocytes-CD14+_RO01746	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links