Variant report

Variant	rs7796389
Chromosome Location	chr7:11444501-11444502
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	MAFK	chr7:11443936-11444546	GM12878	blood:	n/a	chr7:11444296-11444310 chr7:11444298-11444313 chr7:11444295-11444311 chr7:11444293-11444313
2	EP300	chr7:11443029-11445030	SK-N-SH	brain:	n/a	chr7:11443698-11443708 chr7:11444276-11444285 chr7:11444275-11444289 chr7:11444780-11444794 chr7:11443615-11443629

Variant related genes	Relation type
ENSG00000230435	TF binding region

Extended variants
information (count: 43 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:28)

rs_ID	r²[population]
rs10950347	0.82[EUR][1000 genomes]
rs10950348	0.84[EUR][1000 genomes]
rs12670599	0.89[CHB][hapmap]
rs1468244	0.92[CEU][hapmap];0.95[JPT][hapmap];0.84[AMR][1000 genomes];0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1476566	0.95[CEU][hapmap];0.87[CHB][hapmap];0.95[JPT][hapmap];0.90[AFR][1000 genomes];0.89[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs17623777	0.90[CHB][hapmap]
rs1859225	0.88[EUR][1000 genomes]
rs1859226	0.92[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap];0.92[YRI][hapmap];0.81[AFR][1000 genomes];0.86[AMR][1000 genomes];0.82[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1968059	0.92[CEU][hapmap];0.95[JPT][hapmap];0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1978137	0.89[CHB][hapmap]
rs2018144	0.89[CHB][hapmap];0.95[JPT][hapmap];0.83[ASN][1000 genomes]
rs2023868	0.92[CEU][hapmap];0.95[JPT][hapmap];0.93[YRI][hapmap];0.82[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2023869	0.94[JPT][hapmap];0.82[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2189352	0.89[JPT][hapmap]
rs2285757	0.89[JPT][hapmap];0.82[YRI][hapmap]
rs2301743	0.92[CEU][hapmap];0.82[EUR][1000 genomes]
rs2354373	0.91[CEU][hapmap]
rs4636088	0.87[ASN][1000 genomes]
rs4720983	0.92[CEU][hapmap];0.95[JPT][hapmap];0.87[YRI][hapmap];0.85[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs58102730	0.82[EUR][1000 genomes]
rs6956916	0.89[CHB][hapmap]
rs6975177	0.89[CHB][hapmap]
rs6975407	0.92[CEU][hapmap];0.95[JPT][hapmap];0.96[YRI][hapmap];0.82[AFR][1000 genomes];0.85[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7777321	0.89[CHB][hapmap];0.93[YRI][hapmap];0.86[AFR][1000 genomes];0.85[EUR][1000 genomes]
rs7804531	0.83[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs7810604	0.89[CHB][hapmap]
rs7811313	0.90[CHB][hapmap];0.87[YRI][hapmap]
rs984239	0.89[AFR][1000 genomes];0.89[EUR][1000 genomes];0.91[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:15 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1019888	chr7:10712858-11496785	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
2	nsv1029836	chr7:10713523-11492751	Flanking Active TSS Weak transcription Enhancers Strong transcription Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
3	nsv538730	chr7:10713523-11492751	Weak transcription Strong transcription Active TSS Bivalent Enhancer Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
4	nsv1024171	chr7:10810444-11559156	Enhancers Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
5	nsv817291	chr7:10875417-11562683	Weak transcription Enhancers ZNF genes & repeats Active TSS Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
6	nsv523279	chr7:11198193-11473561	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
7	nsv518180	chr7:11198193-11475819	Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
8	nsv1015837	chr7:11208733-11475112	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
9	nsv538732	chr7:11208733-11475112	Enhancers Weak transcription Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
10	nsv1028326	chr7:11221209-11754436	Enhancers Strong transcription Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
11	nsv538733	chr7:11221209-11754436	Weak transcription Strong transcription Flanking Active TSS Enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
12	nsv830902	chr7:11336527-11523904	Flanking Active TSS Enhancers Weak transcription Strong transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
13	nsv830903	chr7:11384957-11586376	Flanking Active TSS Weak transcription ZNF genes & repeats Enhancers Strong transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
14	nsv1032865	chr7:11395480-11477467	Weak transcription ZNF genes & repeats Enhancers Strong transcription Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
15	esv3346993	chr7:11430761-11447799	Strong transcription Weak transcription ZNF genes & repeats Enhancers Genic enhancers	TF binding region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:22 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:11428400-11445600	Weak transcription	Fetal Brain Male	brain
2	chr7:11431200-11461600	Weak transcription	A549	lung
3	chr7:11431600-11445800	Weak transcription	Ovary	ovary
4	chr7:11431600-11446000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr7:11432200-11453200	Weak transcription	Cortex derived primary cultured neurospheres	brain
6	chr7:11432400-11447400	Weak transcription	Brain Cingulate Gyrus	brain
7	chr7:11432600-11445600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
8	chr7:11433000-11453400	Weak transcription	Fetal Stomach	stomach
9	chr7:11434400-11446400	Weak transcription	Adipose Nuclei	Adipose
10	chr7:11435800-11453200	Weak transcription	Primary hematopoietic stem cells	blood
11	chr7:11438600-11459800	Weak transcription	Fetal Brain Female	brain
12	chr7:11440800-11446400	Weak transcription	Fetal Kidney	kidney
13	chr7:11442200-11447400	Strong transcription	Placenta	Placenta
14	chr7:11442800-11456600	Weak transcription	Brain Anterior Caudate	brain
15	chr7:11443400-11456800	Weak transcription	Brain Inferior Temporal Lobe	brain
16	chr7:11443800-11444800	Enhancers	Liver	Liver
17	chr7:11444000-11444800	Enhancers	Fetal Intestine Large	intestine
18	chr7:11444000-11444800	Enhancers	Fetal Intestine Small	intestine
19	chr7:11444200-11445600	Weak transcription	Fetal Lung	lung
20	chr7:11444200-11447800	Weak transcription	Gastric	stomach
21	chr7:11444200-11459800	Weak transcription	Left Ventricle	heart
22	chr7:11444400-11450400	Weak transcription	Brain Germinal Matrix	brain

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