Variant report

Variant	rs201876447
Chromosome Location	chr7:150692630-150692631
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:150671828..150674694-chr7:150692153..150695076,2	MCF-7	breast:

Extended variants
information (count: 17 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:17 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv608990	chr7:149961274-150707488	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Weak transcription ZNF genes & repeats Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	90 gene(s)	inside rSNPs	diseases
2	nsv1030109	chr7:150312916-150701010	Enhancers Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
3	esv1821419	chr7:150593315-150974269	Enhancers Strong transcription Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	128 gene(s)	inside rSNPs	diseases
4	nsv1022246	chr7:150619660-150779924	Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Genic enhancers Enhancers Weak transcription Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
5	nsv889463	chr7:150640285-150700946	Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Bivalent/Poised TSS Weak transcription Bivalent Enhancer Genic enhancers Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region miRNA target site	20 gene(s)	inside rSNPs	diseases
6	nsv889464	chr7:150640285-150723467	Enhancers Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
7	nsv889465	chr7:150640285-150800823	Flanking Active TSS Strong transcription Enhancers Flanking Bivalent TSS/Enh Genic enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	59 gene(s)	inside rSNPs	diseases
8	nsv1017863	chr7:150643928-150779924	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	52 gene(s)	inside rSNPs	diseases
9	nsv539197	chr7:150643928-150779924	Bivalent/Poised TSS Active TSS Strong transcription Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	52 gene(s)	inside rSNPs	diseases
10	nsv1028645	chr7:150643928-150806534	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Active TSS Strong transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	59 gene(s)	inside rSNPs	diseases
11	nsv539198	chr7:150643928-150879259	Weak transcription Enhancers Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	72 gene(s)	inside rSNPs	diseases
12	nsv889467	chr7:150645534-150723467	Weak transcription Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
13	nsv889468	chr7:150652419-150696111	Weak transcription Flanking Bivalent TSS/Enh Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	20 gene(s)	inside rSNPs	diseases
14	nsv889469	chr7:150657209-150747746	Flanking Bivalent TSS/Enh Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
15	nsv889470	chr7:150667210-150696111	Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	18 gene(s)	inside rSNPs	diseases
16	esv3392470	chr7:150691544-150694892	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Active TSS Bivalent/Poised TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases
17	esv3405396	chr7:150691819-150695017	Flanking Bivalent TSS/Enh Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:150686200-150698000	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr7:150688800-150697200	Weak transcription	Pancreas	Pancrea
3	chr7:150690000-150692800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr7:150690400-150692800	Enhancers	Fetal Lung	lung
5	chr7:150691200-150692800	Enhancers	Primary monocytes fromperipheralblood	blood
6	chr7:150691200-150693800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr7:150691400-150694000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
8	chr7:150691800-150692800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr7:150692200-150692800	Enhancers	Fetal Stomach	stomach
10	chr7:150692200-150693400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
11	chr7:150692200-150693800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
12	chr7:150692200-150700800	Weak transcription	Gastric	stomach
13	chr7:150692200-150705000	Weak transcription	Ovary	ovary
14	chr7:150692400-150692800	Enhancers	Primary hematopoietic stem cells short term culture	blood
15	chr7:150692400-150692800	Enhancers	Primary T helper naive cells from peripheral blood	blood
16	chr7:150692400-150692800	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
17	chr7:150692400-150692800	Enhancers	Primary T killer memory cells from peripheral blood	blood
18	chr7:150692400-150692800	Enhancers	Monocytes-CD14+_RO01746	blood
19	chr7:150692400-150693400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr7:150692400-150693400	Weak transcription	Fetal Intestine Large	intestine
21	chr7:150692400-150693400	Weak transcription	Fetal Intestine Small	intestine
22	chr7:150692400-150693600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr7:150692400-150693600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
24	chr7:150692400-150693800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
25	chr7:150692400-150694000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
26	chr7:150692400-150694400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
27	chr7:150692400-150697000	Enhancers	Primary T regulatory cells fromperipheralblood	blood
28	chr7:150692400-150698400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
29	chr7:150692400-150704200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
30	chr7:150692400-150704400	Weak transcription	Right Atrium	heart
31	chr7:150692600-150692800	Enhancers	Primary T cells from cord blood	blood
32	chr7:150692600-150692800	Enhancers	Fetal Muscle Leg	muscle
33	chr7:150692600-150692800	Enhancers	Placenta	Placenta
34	chr7:150692600-150692800	Enhancers	Lung	lung
35	chr7:150692600-150692800	Enhancers	HUVEC	blood vessel
36	chr7:150692600-150693000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr7:150692600-150693400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
38	chr7:150692600-150693400	Weak transcription	Right Ventricle	heart
39	chr7:150692600-150693400	Weak transcription	Spleen	Spleen
40	chr7:150692600-150693600	Weak transcription	Adipose Nuclei	Adipose
41	chr7:150692600-150693600	Weak transcription	K562	blood
42	chr7:150692600-150693800	Weak transcription	H1 Cell Line	embryonic stem cell
43	chr7:150692600-150693800	Weak transcription	HUES6 Cell Line	embryonic stem cell
44	chr7:150692600-150693800	Weak transcription	Primary hematopoietic stem cells	blood
45	chr7:150692600-150694800	Weak transcription	Fetal Heart	heart
46	chr7:150692600-150695000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
47	chr7:150692600-150697800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
48	chr7:150692600-150698200	Enhancers	Primary T helper cells PMA-I stimulated	--
49	chr7:150692600-150698200	Enhancers	Primary T helper cells fromperipheralblood	blood
50	chr7:150692600-150704000	Weak transcription	Left Ventricle	heart

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links