Variant report

Variant	rs6952698
Chromosome Location	chr7:121786341-121786342
allele	A/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	JUN	chr7:121786260-121786389	K562	blood:	n/a	n/a

Variant related genes	Relation type
AASS	TF binding region

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

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

rs_ID	r²[population]
rs10488107	0.82[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs11977512	0.87[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs12113399	0.81[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs12530583	0.87[ASN][1000 genomes]
rs12538079	0.82[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs17616983	0.82[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs2109333	0.82[AFR][1000 genomes];0.90[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2268077	0.87[ASN][1000 genomes]
rs2300199	0.87[ASN][1000 genomes]
rs4727938	0.82[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs57341517	0.85[AFR][1000 genomes];0.82[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs59110694	0.81[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs59224714	0.85[AFR][1000 genomes];0.82[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs59529453	0.82[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs59993706	0.84[ASN][1000 genomes]
rs60159595	0.87[ASN][1000 genomes]
rs61624073	0.85[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs6948443	0.88[AFR][1000 genomes];0.90[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6954944	0.82[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs72499551	0.81[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs73224332	0.82[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs73224336	0.82[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs73224339	0.82[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs73226257	0.82[AFR][1000 genomes];0.90[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73226277	0.87[AMR][1000 genomes];0.81[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs73226300	0.84[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs7784030	0.87[AMR][1000 genomes];0.82[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7810763	0.87[AMR][1000 genomes];0.94[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv427803	chr7:121701581-121876302	Active TSS Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv1019004	chr7:121733372-121800380	ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Weak transcription Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv1034553	chr7:121734934-121800380	Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv523632	chr7:121754695-121802068	Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	nsv1016617	chr7:121770441-121820730	Enhancers Active TSS Flanking Active TSS Weak transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 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	chr7:121784800-121788200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr7:121785000-121786800	Enhancers	Fetal Intestine Large	intestine
3	chr7:121785000-121786800	Enhancers	Fetal Intestine Small	intestine
4	chr7:121785000-121787000	Weak transcription	Aorta	Aorta
5	chr7:121785000-121796800	Weak transcription	Ovary	ovary
6	chr7:121785200-121786800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
7	chr7:121785200-121787600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
8	chr7:121785200-121789800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr7:121785400-121786600	Weak transcription	H9 Cell Line	embryonic stem cell
10	chr7:121785400-121787000	Enhancers	iPS-18 Cell Line	embryonic stem cell
11	chr7:121785400-121791000	Enhancers	ES-I3 Cell Line	embryonic stem cell
12	chr7:121785400-121791800	Enhancers	iPS-15b Cell Line	embryonic stem cell
13	chr7:121785600-121786600	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
14	chr7:121785800-121786600	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
15	chr7:121785800-121786800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
16	chr7:121785800-121786800	Flanking Active TSS	Fetal Heart	heart
17	chr7:121785800-121799600	Weak transcription	Left Ventricle	heart
18	chr7:121785800-121806400	Weak transcription	Pancreas	Pancrea
19	chr7:121786200-121788000	Enhancers	H1 Cell Line	embryonic stem cell
20	chr7:121786200-121789200	Enhancers	HUES48 Cell Line	embryonic stem cell
21	chr7:121786200-121790200	Enhancers	HUES6 Cell Line	embryonic stem cell
22	chr7:121786200-121791600	Weak transcription	Liver	Liver

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