Variant report

Variant	rs547772793
Chromosome Location	chr7:100318743-100318744
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr7:100317495..100321039-chr7:100423744..100425687,3	MCF-7	breast:
2	chr7:100302553..100308135-chr7:100314195..100322207,16	MCF-7	breast:
3	chr7:100302051..100306591-chr7:100312993..100321692,11	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-EPO-1	chr7:100318312-100318821	expReg_chr7_6636_+

Variant related genes	Relation type
ENSG00000146828	Chromatin interaction
ENSG00000172336	Chromatin interaction
ENSG00000196411	Chromatin interaction

Extended variants
information (count: 11 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv1829095	chr7:99814675-100494084	Bivalent Enhancer Active TSS Weak transcription Strong transcription Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	393 gene(s)	inside rSNPs	diseases
2	nsv831072	chr7:100162503-100362835	Enhancers Weak transcription Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	82 gene(s)	inside rSNPs	diseases
3	nsv888791	chr7:100221867-100371114	Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
4	nsv607933	chr7:100240191-100365613	Enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
5	nsv470381	chr7:100240191-100431980	Strong transcription Active TSS Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
6	nsv8184	chr7:100240737-100345945	Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Active TSS Strong transcription Enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
7	nsv888792	chr7:100252918-100329189	Enhancers Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
8	esv1804951	chr7:100275135-100374093	Weak transcription Flanking Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Enhancers Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
9	nsv1020837	chr7:100313122-100508635	Genic enhancers Weak transcription Active TSS Strong transcription Enhancers Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	92 gene(s)	inside rSNPs	diseases
10	nsv888796	chr7:100313420-100423365	Genic enhancers Strong transcription Bivalent Enhancer Weak transcription Enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
11	esv3410635	chr7:100317416-100319614	Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Enhancers Weak transcription Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:55 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:100317200-100319400	Bivalent Enhancer	Fetal Intestine Small	intestine
2	chr7:100317400-100318800	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
3	chr7:100317600-100319400	Bivalent Enhancer	Placenta Amnion	Placenta Amnion
4	chr7:100317800-100318800	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
5	chr7:100317800-100318800	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
6	chr7:100317800-100318800	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
7	chr7:100317800-100318800	Bivalent/Poised TSS	ES-UCSF4 Cell Line	embryonic stem cell
8	chr7:100317800-100318800	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin02	Skin
9	chr7:100317800-100318800	Flanking Bivalent TSS/Enh	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr7:100317800-100318800	Bivalent Enhancer	Fetal Heart	heart
11	chr7:100317800-100319000	Bivalent Enhancer	Primary hematopoietic stem cells	blood
12	chr7:100317800-100319000	Bivalent Enhancer	Stomach Smooth Muscle	stomach
13	chr7:100317800-100319200	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
14	chr7:100317800-100319200	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
15	chr7:100317800-100319200	Flanking Bivalent TSS/Enh	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr7:100317800-100319400	Bivalent Enhancer	Fetal Muscle Leg	muscle
17	chr7:100317800-100321000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
18	chr7:100318000-100318800	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
19	chr7:100318000-100318800	Bivalent Enhancer	Primary B cells from peripheral blood	blood
20	chr7:100318000-100318800	Flanking Bivalent TSS/Enh	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr7:100318000-100318800	Enhancers	Ovary	ovary
22	chr7:100318000-100318800	Active TSS	Right Ventricle	heart
23	chr7:100318000-100319000	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell
24	chr7:100318000-100319000	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
25	chr7:100318000-100319000	Bivalent Enhancer	Fetal Stomach	stomach
26	chr7:100318000-100319200	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
27	chr7:100318000-100319400	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr7:100318000-100319600	Enhancers	Pancreas	Pancrea
29	chr7:100318000-100319800	Bivalent Enhancer	Colonic Mucosa	Colon
30	chr7:100318200-100318800	Bivalent/Poised TSS	iPS DF 6.9 Cell Line	embryonic stem cell
31	chr7:100318200-100318800	Bivalent Enhancer	Primary hematopoietic stem cells short term culture	blood
32	chr7:100318200-100318800	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
33	chr7:100318200-100318800	Active TSS	Right Atrium	heart
34	chr7:100318400-100318800	Bivalent/Poised TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
35	chr7:100318400-100318800	Enhancers	Gastric	stomach
36	chr7:100318400-100319000	Bivalent Enhancer	Spleen	Spleen
37	chr7:100318400-100319200	Bivalent Enhancer	Primary T helper cells fromperipheralblood	blood
38	chr7:100318400-100319400	Flanking Active TSS	Liver	Liver
39	chr7:100318600-100318800	Flanking Bivalent TSS/Enh	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
40	chr7:100318600-100318800	Flanking Bivalent TSS/Enh	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
41	chr7:100318600-100318800	Bivalent Enhancer	Primary T killer naive cells fromperipheralblood	blood
42	chr7:100318600-100318800	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
43	chr7:100318600-100318800	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr7:100318600-100318800	Bivalent/Poised TSS	Ganglion Eminence derived primary cultured neurospheres	brain
45	chr7:100318600-100318800	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
46	chr7:100318600-100318800	Bivalent Enhancer	Brain Dorsolateral Prefrontal Cortex	brain
47	chr7:100318600-100318800	Flanking Bivalent TSS/Enh	Fetal Adrenal Gland	Adrenal Gland
48	chr7:100318600-100318800	Flanking Bivalent TSS/Enh	Placenta	Placenta
49	chr7:100318600-100319000	Bivalent Enhancer	ES-WA7 Cell Line	embryonic stem cell
50	chr7:100318600-100319000	Bivalent Enhancer	Primary T helper naive cells fromperipheralblood	blood

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