Variant report

Variant	rs500382
Chromosome Location	chr3:54663424-54663425
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 20 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs13084347	0.81[AMR][1000 genomes]
rs1366032	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs495532	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs4955988	0.84[CEU][hapmap];0.85[AMR][1000 genomes]
rs496625	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs499292	1.00[CHB][hapmap];0.95[JPT][hapmap];0.98[ASN][1000 genomes]
rs573279	1.00[CEU][hapmap];0.91[JPT][hapmap];1.00[YRI][hapmap]
rs595993	0.95[CHB][hapmap];0.95[JPT][hapmap];0.81[YRI][hapmap];0.90[ASN][1000 genomes]
rs605284	0.82[CHB][hapmap];0.85[JPT][hapmap]
rs616113	0.95[ASN][1000 genomes]
rs661201	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs662565	0.90[AMR][1000 genomes];0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs662982	0.81[AMR][1000 genomes];0.80[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs667612	0.82[CHB][hapmap];0.91[JPT][hapmap]
rs674542	0.95[ASN][1000 genomes]
rs71301895	0.82[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	nsv1014595	chr3:53944473-54846754	Enhancers Bivalent Enhancer Weak transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv428084	chr3:54404258-54742756	Weak transcription Enhancers Active TSS Genic enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv834700	chr3:54637374-54803896	Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv525644	chr3:54653316-54709987	Weak transcription Genic enhancers Enhancers Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:23 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:54651000-54666400	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr3:54652800-54665000	Weak transcription	Skeletal Muscle Female	skeletal muscle
3	chr3:54654000-54667000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr3:54659200-54664600	Weak transcription	Fetal Muscle Leg	muscle
5	chr3:54659800-54664400	Weak transcription	Spleen	Spleen
6	chr3:54660400-54666800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr3:54662400-54663600	Strong transcription	Stomach Smooth Muscle	stomach
8	chr3:54662400-54664600	Enhancers	HMEC	breast
9	chr3:54662400-54665200	Strong transcription	Right Atrium	heart
10	chr3:54662600-54664000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr3:54662600-54664200	Weak transcription	H1 Cell Line	embryonic stem cell
12	chr3:54662800-54663600	Strong transcription	Ovary	ovary
13	chr3:54662800-54663600	Enhancers	Hela-S3	cervix
14	chr3:54662800-54663800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr3:54663000-54663800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr3:54663000-54663800	Enhancers	Esophagus	oesophagus
17	chr3:54663000-54664800	Enhancers	iPS-20b Cell Line	embryonic stem cell
18	chr3:54663000-54666200	Weak transcription	Brain Anterior Caudate	brain
19	chr3:54663000-54667800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
20	chr3:54663200-54664200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
21	chr3:54663200-54665000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr3:54663200-54667400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
23	chr3:54663400-54664400	Enhancers	HUES48 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links