Variant report

Variant	rs9993085
Chromosome Location	chr4:7939034-7939035
allele	C/T
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	CHD1	chr4:7938516-7942221	IMR90	lung:	n/a	n/a
2	POLR2A	chr4:7938953-7939381	PANC-1	pancreas:	n/a	n/a
3	EP300	chr4:7938724-7939097	Hela-S3	cervix:	n/a	chr4:7938979-7938993
4	CEBPB	chr4:7938723-7939060	IMR90	lung:	n/a	n/a
5	POLR2A	chr4:7938761-7939283	IMR90	lung:	n/a	n/a
6	CEBPB	chr4:7938700-7939075	Hela-S3	cervix:	n/a	n/a
7	EP300	chr4:7938830-7939077	K562	blood:	n/a	chr4:7938979-7938993

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr4:7799366..7802066-chr4:7938906..7941900,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000228919	TF binding region
ENSG00000196526	Chromatin interaction

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

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs12696835	0.85[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1344223	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2385912	0.80[AMR][1000 genomes];0.93[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2385914	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs28446696	0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs34072960	0.81[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs58349148	0.84[EUR][1000 genomes]
rs66479458	0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6840305	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6846757	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7669433	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7669645	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7695142	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7695170	0.88[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7698368	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[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	nsv491712	chr4:7582506-8155069	Enhancers Bivalent Enhancer Genic enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
2	esv34140	chr4:7787936-8172491	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	18 gene(s)	inside rSNPs	diseases
3	esv2754386	chr4:7822449-7992909	Weak transcription Enhancers Active TSS Genic enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	esv2756298	chr4:7822449-7992909	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
5	nsv878578	chr4:7841833-7969594	Enhancers Flanking Active TSS Genic enhancers Weak transcription ZNF genes & repeats Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:88 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:7931400-7939800	Weak transcription	Fetal Kidney	kidney
2	chr4:7931600-7939600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
3	chr4:7931600-7939600	Weak transcription	Ovary	ovary
4	chr4:7931600-7939600	Weak transcription	Skeletal Muscle Female	skeletal muscle
5	chr4:7931600-7939800	Weak transcription	Lung	lung
6	chr4:7931800-7939600	Weak transcription	Brain Angular Gyrus	brain
7	chr4:7932000-7939600	Weak transcription	Brain Anterior Caudate	brain
8	chr4:7932000-7939600	Weak transcription	Duodenum Mucosa	Duodenum
9	chr4:7932000-7939600	Weak transcription	Left Ventricle	heart
10	chr4:7932000-7939600	Weak transcription	NHLF	lung
11	chr4:7932000-7939800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
12	chr4:7932000-7939800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr4:7932000-7939800	Weak transcription	Small Intestine	intestine
14	chr4:7932200-7939600	Weak transcription	HUES48 Cell Line	embryonic stem cell
15	chr4:7932200-7939600	Weak transcription	Rectal Mucosa Donor 31	rectum
16	chr4:7932200-7939800	Weak transcription	H1 Cell Line	embryonic stem cell
17	chr4:7932200-7939800	Weak transcription	Pancreas	Pancrea
18	chr4:7932400-7939600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr4:7932800-7939600	Weak transcription	Primary T cells fromperipheralblood	blood
20	chr4:7935400-7939600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
21	chr4:7935600-7939600	Weak transcription	Aorta	Aorta
22	chr4:7935600-7939600	Enhancers	HSMMtube	muscle
23	chr4:7935800-7939600	Weak transcription	Placenta	Placenta
24	chr4:7936200-7939600	Weak transcription	Placenta Amnion	Placenta Amnion
25	chr4:7936200-7939800	Weak transcription	Right Ventricle	heart
26	chr4:7936400-7939200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
27	chr4:7936400-7939400	Weak transcription	Fetal Stomach	stomach
28	chr4:7936400-7939600	Weak transcription	Fetal Intestine Small	intestine
29	chr4:7936400-7939600	Weak transcription	Stomach Mucosa	stomach
30	chr4:7936400-7939800	Weak transcription	Esophagus	oesophagus
31	chr4:7936600-7939400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
32	chr4:7936600-7939600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
33	chr4:7936600-7939800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
34	chr4:7936600-7939800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr4:7936600-7939800	Weak transcription	Gastric	stomach
36	chr4:7936800-7939200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
37	chr4:7937000-7939600	Enhancers	Cortex derived primary cultured neurospheres	brain
38	chr4:7937200-7939200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
39	chr4:7937200-7939200	Flanking Active TSS	Osteobl	bone
40	chr4:7937200-7939600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
41	chr4:7937400-7939200	Flanking Active TSS	HUVEC	blood vessel
42	chr4:7937400-7939800	Enhancers	Primary T helper cells fromperipheralblood	blood
43	chr4:7937600-7939400	Enhancers	Primary monocytes fromperipheralblood	blood
44	chr4:7937600-7939600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
45	chr4:7937800-7939200	Enhancers	Hela-S3	cervix
46	chr4:7937800-7939600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr4:7937800-7941800	Active TSS	A549	lung
48	chr4:7938000-7939600	Weak transcription	HUES6 Cell Line	embryonic stem cell
49	chr4:7938000-7939600	Weak transcription	HUES64 Cell Line	embryonic stem cell
50	chr4:7938200-7939400	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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