Variant report

Variant	rs7732731
Chromosome Location	chr5:112115743-112115744
allele	G/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	FOS	chr5:112115192-112115782	MCF10A-Er-Src	breast:	n/a	n/a
2	POLR2A	chr5:112115675-112115793	GM12878	blood:	n/a	n/a
3	FOS	chr5:112115189-112115782	MCF10A-Er-Src	breast:	n/a	n/a
4	FOS	chr5:112115185-112115782	MCF10A-Er-Src	breast:	n/a	n/a

Variant related genes	Relation type
CBX3P3	TF binding region

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

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs35043160	1.00[AMR][1000 genomes]
rs58000594	1.00[AMR][1000 genomes]
rs6877425	1.00[AMR][1000 genomes]
rs6883262	1.00[AMR][1000 genomes]
rs6897222	1.00[AMR][1000 genomes]
rs73214318	1.00[AMR][1000 genomes]
rs73216232	1.00[AMR][1000 genomes]
rs73218106	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73218111	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73218123	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73220029	1.00[AMR][1000 genomes]
rs9686237	0.81[AFR][1000 genomes]
rs9686520	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv830450	chr5:111964170-112134510	Active TSS Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
2	nsv462387	chr5:112053911-112124369	Flanking Active TSS Enhancers Active TSS Weak transcription Strong transcription Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	8 gene(s)	inside rSNPs	diseases
3	nsv599393	chr5:112053911-112124369	Strong transcription Active TSS Weak transcription Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	8 gene(s)	inside rSNPs	diseases
4	nsv1032464	chr5:112076061-112192380	Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	11 gene(s)	inside rSNPs	diseases
5	nsv537862	chr5:112076061-112192380	Weak transcription Genic enhancers Strong transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	11 gene(s)	inside rSNPs	diseases
6	esv33290	chr5:112110808-112238295	Weak transcription Strong transcription Flanking Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
7	nsv1029271	chr5:112113308-112325943	Strong transcription Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:121 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:112074400-112119800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
2	chr5:112074400-112125600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr5:112074400-112128600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
4	chr5:112079600-112128200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
5	chr5:112079800-112128600	Weak transcription	Small Intestine	intestine
6	chr5:112081200-112128600	Weak transcription	H9 Cell Line	embryonic stem cell
7	chr5:112087600-112117600	Weak transcription	Gastric	stomach
8	chr5:112089800-112116600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
9	chr5:112093400-112116000	Weak transcription	HUVEC	blood vessel
10	chr5:112093400-112117400	Weak transcription	Rectal Smooth Muscle	rectum
11	chr5:112093400-112128600	Weak transcription	Ovary	ovary
12	chr5:112093400-112128600	Weak transcription	Skeletal Muscle Male	skeletal muscle
13	chr5:112093400-112183800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
14	chr5:112094200-112128600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
15	chr5:112094200-112128800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
16	chr5:112095200-112122400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr5:112095600-112116800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
18	chr5:112096200-112116000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
19	chr5:112096200-112117600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
20	chr5:112097000-112116600	Weak transcription	Brain Hippocampus Middle	brain
21	chr5:112097800-112127000	Weak transcription	Esophagus	oesophagus
22	chr5:112098000-112128600	Weak transcription	HepG2	liver
23	chr5:112098200-112128600	Weak transcription	Aorta	Aorta
24	chr5:112098200-112129800	Weak transcription	Spleen	Spleen
25	chr5:112098400-112130000	Weak transcription	Fetal Heart	heart
26	chr5:112098600-112116400	Weak transcription	Placenta	Placenta
27	chr5:112098600-112131400	Weak transcription	Pancreatic Islets	Pancreatic Islet
28	chr5:112098800-112122400	Weak transcription	A549	lung
29	chr5:112099600-112122200	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr5:112100000-112152200	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
31	chr5:112101200-112117400	Weak transcription	Pancreas	Pancrea
32	chr5:112101600-112118000	Strong transcription	Primary B cells from peripheral blood	blood
33	chr5:112102200-112120400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr5:112102400-112118400	Strong transcription	Dnd41	blood
35	chr5:112102400-112121000	Strong transcription	Primary neutrophils fromperipheralblood	blood
36	chr5:112102600-112118400	Strong transcription	Primary T cells fromperipheralblood	blood
37	chr5:112102800-112119000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
38	chr5:112103000-112173200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr5:112104400-112125600	Weak transcription	Fetal Intestine Small	intestine
40	chr5:112104600-112116400	Weak transcription	Fetal Kidney	kidney
41	chr5:112104600-112116800	Weak transcription	HUES6 Cell Line	embryonic stem cell
42	chr5:112104600-112117400	Weak transcription	H1 Cell Line	embryonic stem cell
43	chr5:112104600-112117400	Weak transcription	Lung	lung
44	chr5:112104600-112128600	Weak transcription	Colon Smooth Muscle	Colon
45	chr5:112104600-112155400	Weak transcription	Psoas Muscle	Psoas
46	chr5:112104800-112128000	Weak transcription	Hela-S3	cervix
47	chr5:112104800-112130800	Weak transcription	Stomach Mucosa	stomach
48	chr5:112105000-112128600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
49	chr5:112105000-112128600	Weak transcription	Thymus	Thymus
50	chr5:112105200-112116600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell

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