Variant report

Variant	rs62337068
Chromosome Location	chr5:1930567-1930568
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	NR2C2	chr5:1929198-1930575	GM12878	blood:	n/a	n/a
2	POLR2A	chr5:1930367-1930578	MCF-7	breast:	n/a	n/a
3	POLR2A	chr5:1927991-1933825	MCF10A-Er-Src	breast:	n/a	n/a
4	POLR2A	chr5:1928300-1932687	MCF10A-Er-Src	breast:	n/a	n/a
5	SUZ12	chr5:1929166-1930596	H1-hESC	embryonic stem cell:	n/a	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr5:1928752..1930799-chr5:1946292..1948777,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-IRX4-2	chr5:1930518-1930577	XLOC_004707

Variant related genes	Relation type
ENSG00000248994	TF binding region

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

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs10462748	0.82[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs11949902	0.84[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs11952878	0.81[ASN][1000 genomes]
rs13162440	0.80[ASN][1000 genomes]
rs16901995	0.82[AMR][1000 genomes]
rs4478361	0.84[ASN][1000 genomes]
rs4975766	0.80[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs6420032	0.82[ASN][1000 genomes]
rs6420033	0.82[ASN][1000 genomes]
rs6555024	0.80[ASN][1000 genomes]
rs6555025	0.81[ASN][1000 genomes]
rs6555026	0.81[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs6555027	0.85[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs6555029	0.85[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs6865822	0.82[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs6881134	0.82[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs6890530	0.80[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs6897356	0.85[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs7444179	0.81[ASN][1000 genomes]
rs7444647	0.85[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs7713748	0.81[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:22 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv933805	chr5:1450724-1941619	Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Strong transcription Active TSS Weak transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	96 gene(s)	inside rSNPs	diseases
2	nsv817407	chr5:1495354-2191460	Weak transcription Strong transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	107 gene(s)	inside rSNPs	diseases
3	nsv869236	chr5:1719263-2259100	Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Enhancers Weak transcription ZNF genes & repeats Genic enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	66 gene(s)	inside rSNPs	diseases
4	nsv881557	chr5:1822326-1932463	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
5	nsv880886	chr5:1880891-1936443	Bivalent Enhancer Bivalent/Poised TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
6	nsv880460	chr5:1886471-1936443	Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Weak transcription Flanking Active TSS Genic enhancers Active TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
7	nsv915846	chr5:1891098-2167677	Active TSS Genic enhancers Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
8	nsv881650	chr5:1892995-1944487	Enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Active TSS ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
9	nsv880653	chr5:1892995-1946697	Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Weak transcription Bivalent Enhancer Active TSS ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
10	nsv1015576	chr5:1894124-1942909	Active TSS Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
11	nsv880562	chr5:1895829-1936443	Enhancers Weak transcription Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
12	nsv881174	chr5:1895829-1942834	Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Enhancers Active TSS Bivalent Enhancer Weak transcription Flanking Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
13	nsv880381	chr5:1895829-1946697	Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Active TSS Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
14	nsv1026930	chr5:1898993-2126061	Bivalent/Poised TSS Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
15	nsv508344	chr5:1905222-1976860	Enhancers Active TSS Weak transcription ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
16	nsv881562	chr5:1907974-1976187	Enhancers Weak transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
17	nsv880964	chr5:1912921-1953161	Weak transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
18	nsv596897	chr5:1924628-1934490	Bivalent Enhancer Bivalent/Poised TSS Enhancers Genic enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
19	esv3429117	chr5:1927452-1931450	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Weak transcription Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
20	esv3379236	chr5:1927852-1931550	Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
21	esv3382920	chr5:1927852-1931550	Enhancers Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
22	esv3356023	chr5:1930087-1930641	Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Weak transcription Genic enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:47 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:1929200-1930600	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
2	chr5:1929200-1930600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr5:1929200-1930600	Flanking Bivalent TSS/Enh	Fetal Kidney	kidney
4	chr5:1929200-1930600	ZNF genes & repeats	Lung	lung
5	chr5:1929200-1930600	Enhancers	Ovary	ovary
6	chr5:1929200-1930800	Enhancers	Right Ventricle	heart
7	chr5:1929600-1931400	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr5:1929800-1931200	Bivalent Enhancer	Fetal Brain Male	brain
9	chr5:1930000-1930600	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
10	chr5:1930000-1930600	Bivalent Enhancer	Primary B cells from peripheral blood	blood
11	chr5:1930000-1930600	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr5:1930200-1930600	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr5:1930200-1930600	Enhancers	Brain Anterior Caudate	brain
14	chr5:1930200-1930600	Bivalent Enhancer	Brain Dorsolateral Prefrontal Cortex	brain
15	chr5:1930200-1930600	Enhancers	Esophagus	oesophagus
16	chr5:1930200-1930600	Flanking Bivalent TSS/Enh	Fetal Heart	heart
17	chr5:1930200-1930600	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
18	chr5:1930200-1930600	Bivalent Enhancer	Skeletal Muscle Female	skeletal muscle
19	chr5:1930200-1930800	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
20	chr5:1930200-1930800	Enhancers	Brain Inferior Temporal Lobe	brain
21	chr5:1930200-1930800	Flanking Bivalent TSS/Enh	Duodenum Mucosa	Duodenum
22	chr5:1930200-1930800	Bivalent Enhancer	Fetal Muscle Leg	muscle
23	chr5:1930200-1930800	Bivalent Enhancer	Fetal Stomach	stomach
24	chr5:1930200-1930800	Enhancers	Left Ventricle	heart
25	chr5:1930200-1932000	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
26	chr5:1930400-1930600	Flanking Bivalent TSS/Enh	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr5:1930400-1930600	Flanking Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr5:1930400-1930600	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr5:1930400-1930600	Bivalent Enhancer	iPS DF 6.9 Cell Line	embryonic stem cell
30	chr5:1930400-1930600	Bivalent Enhancer	Adipose Nuclei	Adipose
31	chr5:1930400-1930600	Bivalent Enhancer	Fetal Brain Female	brain
32	chr5:1930400-1930600	Flanking Bivalent TSS/Enh	Fetal Lung	lung
33	chr5:1930400-1930600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
34	chr5:1930400-1930600	Flanking Bivalent TSS/Enh	Rectal Smooth Muscle	rectum
35	chr5:1930400-1930800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr5:1930400-1930800	Bivalent Enhancer	Brain Cingulate Gyrus	brain
37	chr5:1930400-1930800	Enhancers	Colon Smooth Muscle	Colon
38	chr5:1930400-1930800	Weak transcription	Right Atrium	heart
39	chr5:1930400-1930800	Flanking Bivalent TSS/Enh	Stomach Smooth Muscle	stomach
40	chr5:1930400-1931000	Flanking Active TSS	Pancreas	Pancrea
41	chr5:1930400-1931200	Bivalent Enhancer	Placenta Amnion	Placenta Amnion
42	chr5:1930400-1931600	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
43	chr5:1930400-1931800	Active TSS	Gastric	stomach
44	chr5:1930400-1932200	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
45	chr5:1930400-1932200	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr5:1930400-1932200	Flanking Active TSS	NHEK	skin
47	chr5:1930400-1932400	Flanking Active TSS	HMEC	breast

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