Variant report

Variant	rs532948183
Chromosome Location	chr10:21798967-21798968
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr10:21794668..21800963-chr10:21813670..21817700,8	MCF-7	breast:
2	chr10:21798837..21800885-chr10:21814411..21817123,2	MCF-7	breast:
3	chr10:21798661..21801415-chr10:22093331..22096294,2	K562	blood:
4	chr10:21795681..21797336-chr10:21797733..21799271,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000180592	Chromatin interaction

Extended variants
information (count: 22 )
Associated
traits (count: 0)

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	nsv825284	chr10:21739527-21847437	Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Enhancers Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	34 gene(s)	inside rSNPs	diseases
2	nsv825285	chr10:21742026-21874334	Strong transcription Weak transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	34 gene(s)	inside rSNPs	diseases
3	nsv825286	chr10:21757784-21838890	Flanking Active TSS Bivalent/Poised TSS Weak transcription Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	34 gene(s)	inside rSNPs	diseases
4	nsv825288	chr10:21759085-21831354	Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Enhancers Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	34 gene(s)	inside rSNPs	diseases
5	nsv825289	chr10:21762506-21845875	Strong transcription Enhancers Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	34 gene(s)	inside rSNPs	diseases
6	nsv527055	chr10:21764019-21822856	Bivalent/Poised TSS Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	34 gene(s)	inside rSNPs	diseases
7	nsv825290	chr10:21777857-21830878	Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Bivalent/Poised TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	33 gene(s)	inside rSNPs	diseases
8	nsv894936	chr10:21781589-21827796	Active TSS Bivalent/Poised TSS Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Genic enhancers Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	33 gene(s)	inside rSNPs	diseases
9	nsv550200	chr10:21782842-21824727	Active TSS Bivalent/Poised TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	33 gene(s)	inside rSNPs	diseases
10	nsv894937	chr10:21782842-21827796	Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Bivalent Enhancer Strong transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	33 gene(s)	inside rSNPs	diseases
11	nsv517469	chr10:21783634-21822856	Active TSS Bivalent Enhancer Flanking Active TSS Weak transcription Enhancers Bivalent/Poised TSS 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	33 gene(s)	inside rSNPs	diseases
12	nsv894938	chr10:21784899-21827796	Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	33 gene(s)	inside rSNPs	diseases
13	nsv894939	chr10:21789406-21830104	Bivalent Enhancer Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
14	nsv825291	chr10:21792100-21830946	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
15	nsv894940	chr10:21796081-21823525	Active TSS Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
16	nsv550201	chr10:21796081-21824727	Weak transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
17	nsv894941	chr10:21796081-21827796	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
18	nsv894942	chr10:21798241-21823525	Flanking Active TSS Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
19	nsv894943	chr10:21798241-21824619	Active TSS Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
20	nsv894944	chr10:21798241-21827796	Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer Enhancers Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
21	nsv894945	chr10:21798241-21830104	Active TSS Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
22	nsv894946	chr10:21798241-21831215	Enhancers Bivalent/Poised TSS Weak transcription Flanking Active TSS Strong transcription Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:75 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:21789800-21799800	Weak transcription	Lung	lung
2	chr10:21794600-21799000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
3	chr10:21795000-21799000	Weak transcription	Left Ventricle	heart
4	chr10:21795200-21799000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr10:21795600-21799000	Enhancers	Placenta	Placenta
6	chr10:21795800-21799600	Enhancers	HepG2	liver
7	chr10:21795800-21799800	Enhancers	Fetal Heart	heart
8	chr10:21795800-21799800	Weak transcription	A549	lung
9	chr10:21796400-21801000	Weak transcription	K562	blood
10	chr10:21796600-21799000	Weak transcription	Primary neutrophils fromperipheralblood	blood
11	chr10:21796600-21799000	Enhancers	Fetal Lung	lung
12	chr10:21796800-21800000	Active TSS	ES-WA7 Cell Line	embryonic stem cell
13	chr10:21796800-21801000	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
14	chr10:21797000-21800000	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr10:21797200-21799800	Active TSS	H9 Cell Line	embryonic stem cell
16	chr10:21797200-21800200	Active TSS	ES-I3 Cell Line	embryonic stem cell
17	chr10:21797400-21800200	Active TSS	HUES48 Cell Line	embryonic stem cell
18	chr10:21797400-21806600	Active TSS	Fetal Brain Female	brain
19	chr10:21797600-21799800	Active TSS	iPS-15b Cell Line	embryonic stem cell
20	chr10:21797800-21799000	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr10:21797800-21799000	Enhancers	Placenta Amnion	Placenta Amnion
22	chr10:21798000-21799000	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
23	chr10:21798200-21799200	Flanking Active TSS	Brain Germinal Matrix	brain
24	chr10:21798200-21799600	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr10:21798200-21799800	Active TSS	Brain Inferior Temporal Lobe	brain
26	chr10:21798400-21799000	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin
27	chr10:21798400-21799800	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
28	chr10:21798400-21799800	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
29	chr10:21798400-21800200	Enhancers	Fetal Brain Male	brain
30	chr10:21798600-21799000	Flanking Active TSS	H1 Cell Line	embryonic stem cell
31	chr10:21798600-21799000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
32	chr10:21798600-21799000	Bivalent/Poised TSS	Monocytes-CD14+_RO01746	blood
33	chr10:21798600-21799400	Weak transcription	Fetal Kidney	kidney
34	chr10:21798600-21799400	Bivalent/Poised TSS	Skeletal Muscle Male	skeletal muscle
35	chr10:21798600-21799600	Flanking Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
36	chr10:21798600-21799600	Active TSS	HUES64 Cell Line	embryonic stem cell
37	chr10:21798600-21799600	Active TSS	Brain Anterior Caudate	brain
38	chr10:21798600-21799600	Active TSS	Fetal Intestine Small	intestine
39	chr10:21798600-21799600	Transcr. at gene 5' and 3'	Right Atrium	heart
40	chr10:21798600-21799600	Active TSS	Skeletal Muscle Female	skeletal muscle
41	chr10:21798600-21799800	Active TSS	Breast Myoepithelial Primary Cells	Breast
42	chr10:21798600-21799800	Active TSS	Colon Smooth Muscle	Colon
43	chr10:21798600-21799800	Flanking Active TSS	Fetal Muscle Trunk	muscle
44	chr10:21798600-21800200	Active TSS	HUES6 Cell Line	embryonic stem cell
45	chr10:21798800-21799000	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr10:21798800-21799000	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr10:21798800-21799000	Bivalent/Poised TSS	Foreskin Melanocyte Primary Cells skin01	Skin
48	chr10:21798800-21799000	Flanking Active TSS	Brain Angular Gyrus	brain
49	chr10:21798800-21799000	Weak transcription	Fetal Intestine Large	intestine
50	chr10:21798800-21799000	Active TSS	Fetal Muscle Leg	muscle

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