Variant report

Variant	rs7672782
Chromosome Location	chr4:86579977-86579978
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 33 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs28429534	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28871342	1.00[AMR][1000 genomes]
rs6531840	1.00[ASW][hapmap];0.85[LWK][hapmap];0.91[MKK][hapmap];1.00[YRI][hapmap];0.80[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6813231	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6814544	0.92[YRI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6815200	0.84[YRI][hapmap];1.00[AMR][1000 genomes]
rs6816066	1.00[AMR][1000 genomes]
rs6827386	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6827564	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6858619	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6858779	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7654408	1.00[AMR][1000 genomes]
rs7657112	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7657712	1.00[ASW][hapmap];1.00[LWK][hapmap];1.00[MKK][hapmap];0.92[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7662585	0.85[YRI][hapmap];0.80[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7663051	0.80[AFR][1000 genomes]
rs7667098	1.00[ASW][hapmap];0.85[LWK][hapmap];0.90[MKK][hapmap];1.00[YRI][hapmap];1.00[AMR][1000 genomes]
rs7671828	0.86[YRI][hapmap];0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7672626	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7673815	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7685260	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7685271	0.85[YRI][hapmap];0.80[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7688778	1.00[ASW][hapmap];0.85[LWK][hapmap];0.90[MKK][hapmap];1.00[YRI][hapmap];1.00[AMR][1000 genomes]
rs7689198	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7689606	1.00[AMR][1000 genomes]
rs7690114	1.00[AMR][1000 genomes]
rs7690209	1.00[AMR][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	nsv519588	chr4:85762385-86591202	Weak transcription Enhancers Strong transcription Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
2	nsv461566	chr4:85988032-86725502	Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	5 gene(s)	inside rSNPs	diseases
3	nsv594747	chr4:85988032-86725502	Enhancers Active TSS Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	5 gene(s)	inside rSNPs	diseases
4	nsv470048	chr4:85998783-86720838	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	5 gene(s)	inside rSNPs	diseases
5	esv3450999	chr4:86485840-86773745	Enhancers Weak transcription Genic enhancers Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region miRNA	2 gene(s)	inside rSNPs	diseases
6	nsv829999	chr4:86500257-86666019	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Genic enhancers Strong transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region miRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:21 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:86559800-86580200	Weak transcription	Fetal Muscle Leg	muscle
2	chr4:86561800-86582800	Weak transcription	K562	blood
3	chr4:86570200-86593600	Weak transcription	HSMM	muscle
4	chr4:86572400-86580200	Weak transcription	Pancreas	Pancrea
5	chr4:86577200-86582200	Enhancers	Primary monocytes fromperipheralblood	blood
6	chr4:86577400-86582400	Enhancers	Primary neutrophils fromperipheralblood	blood
7	chr4:86577600-86581600	Enhancers	Primary B cells from peripheral blood	blood
8	chr4:86577600-86582600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr4:86577800-86582600	Enhancers	Primary B cells from cord blood	blood
10	chr4:86578800-86580000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr4:86578800-86581000	Enhancers	GM12878-XiMat	blood
12	chr4:86579000-86581000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
13	chr4:86579000-86581600	Enhancers	Breast Myoepithelial Primary Cells	Breast
14	chr4:86579600-86580000	Enhancers	Monocytes-CD14+_RO01746	blood
15	chr4:86579600-86581800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
16	chr4:86579800-86580200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr4:86579800-86580200	Enhancers	Adipose Nuclei	Adipose
18	chr4:86579800-86580200	Enhancers	Colon Smooth Muscle	Colon
19	chr4:86579800-86580200	Enhancers	Thymus	Thymus
20	chr4:86579800-86580400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
21	chr4:86579800-86580400	Enhancers	Right Atrium	heart

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links