Variant report

Variant	rs7038822
Chromosome Location	chr9:94715035-94715036
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr9:94714238..94717195-chr9:94796671..94799619,2	MCF-7	breast:
2	chr9:94708854..94711565-chr9:94713620..94715763,2	MCF-7	breast:
3	chr9:94714221..94717070-chr9:94719717..94722305,2	K562	blood:

Variant related genes	Relation type
ENSG00000169071	Chromatin interaction

Extended variants
information (count: 48 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:42)

rs_ID	r²[population]
rs10123678	0.82[CEU][hapmap]
rs1573979	0.94[ASN][1000 genomes]
rs16908129	0.83[ASN][1000 genomes]
rs16908147	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1954599	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2001676	1.00[CEU][hapmap]
rs2049704	0.94[ASN][1000 genomes]
rs2049705	1.00[CHB][hapmap];0.86[ASN][1000 genomes]
rs2186091	1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[ASN][1000 genomes]
rs2297569	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs3750441	0.83[ASN][1000 genomes]
rs3858082	1.00[CHB][hapmap];0.86[ASN][1000 genomes]
rs3858086	0.82[CEU][hapmap]
rs59394638	0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs60066947	0.97[ASN][1000 genomes]
rs6479381	0.83[ASN][1000 genomes]
rs6479382	0.83[ASN][1000 genomes]
rs7018784	1.00[CEU][hapmap]
rs7021155	1.00[CEU][hapmap]
rs7021285	0.82[CEU][hapmap]
rs7027257	0.82[CEU][hapmap]
rs7032998	1.00[CHB][hapmap];0.83[ASN][1000 genomes]
rs7033261	1.00[ASN][1000 genomes]
rs7040090	1.00[CEU][hapmap]
rs7046846	1.00[CHB][hapmap];0.86[ASN][1000 genomes]
rs7048052	1.00[CHB][hapmap];0.80[ASN][1000 genomes]
rs7851249	0.82[CEU][hapmap]
rs7851545	1.00[ASN][1000 genomes]
rs7854213	1.00[CEU][hapmap]
rs7854552	0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7854566	0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7854742	0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7857164	0.83[ASN][1000 genomes]
rs7857924	0.86[ASN][1000 genomes]
rs7866188	1.00[CHB][hapmap];0.86[ASN][1000 genomes]
rs7866630	0.83[ASN][1000 genomes]
rs7872177	0.83[ASN][1000 genomes]
rs7873326	0.86[CHB][hapmap];0.83[ASN][1000 genomes]
rs7875069	0.83[ASN][1000 genomes]
rs7875147	0.86[ASN][1000 genomes]
rs7876056	1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[ASN][1000 genomes]
rs7944	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	nsv1047426	chr9:94363211-94758114	Weak transcription Bivalent Enhancer Active TSS Enhancers Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	8 gene(s)	inside rSNPs	diseases
2	nsv949008	chr9:94500776-95182133	Enhancers ZNF genes & repeats Weak transcription Bivalent Enhancer Strong transcription Flanking Active TSS Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	55 gene(s)	inside rSNPs	diseases
3	nsv1050845	chr9:94687959-95312406	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	58 gene(s)	inside rSNPs	diseases
4	nsv1046733	chr9:94690622-95138564	Genic enhancers Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
5	nsv831653	chr9:94692454-94867542	Strong transcription Enhancers Weak transcription Bivalent/Poised TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
6	nsv530947	chr9:94697309-95093377	Weak transcription Bivalent Enhancer Strong transcription Enhancers Active TSS Bivalent/Poised TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	49 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:94711200-94717000	Weak transcription	Fetal Heart	heart
2	chr9:94713000-94716400	Weak transcription	Gastric	stomach
3	chr9:94713400-94716800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
4	chr9:94713400-94720200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr9:94713400-94720600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
6	chr9:94713600-94717200	Weak transcription	Fetal Lung	lung
7	chr9:94713600-94717200	Weak transcription	Placenta Amnion	Placenta Amnion
8	chr9:94713800-94717000	Weak transcription	Rectal Smooth Muscle	rectum
9	chr9:94714200-94715600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr9:94714200-94716600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr9:94714800-94716600	Weak transcription	K562	blood
12	chr9:94714800-94717200	Weak transcription	Adipose Nuclei	Adipose
13	chr9:94714800-94717200	Weak transcription	Pancreas	Pancrea
14	chr9:94715000-94716800	Weak transcription	Stomach Smooth Muscle	stomach

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links