Variant report

Variant	nsv893434
Chromosome Location	chr9:72091413-72134376
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:16)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:16 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:72088172..72090177-chr9:72119590..72122551,2	MCF-7	breast:
2	chr9:72126490..72129215-chr9:72129544..72132569,4	MCF-7	breast:
3	chr9:72089155..72091732-chr9:72106824..72109478,2	MCF-7	breast:
4	chr9:72099255..72100862-chr9:72117750..72119500,2	MCF-7	breast:
5	chr9:72098831..72100503-chr9:72120147..72122522,2	MCF-7	breast:
6	chr9:72086703..72089641-chr9:72090516..72093121,4	MCF-7	breast:
7	chr9:72098374..72100350-chr9:72107226..72109233,2	MCF-7	breast:
8	chr9:72126490..72129215-chr9:72129544..72132569,4	MCF-7	breast:
9	chr9:72113417..72115409-chr9:72425666..72428097,2	K562	blood:
10	chr9:72099255..72100862-chr9:72117750..72119500,2	MCF-7	breast:
11	chr9:72098831..72100503-chr9:72120147..72122522,2	MCF-7	breast:
12	chr9:72108434..72110396-chr9:72113331..72115330,2	MCF-7	breast:
13	chr9:72098374..72100350-chr9:72107226..72109233,2	MCF-7	breast:
14	chr9:72089155..72091732-chr9:72106824..72109478,2	MCF-7	breast:
15	chr9:72108434..72110396-chr9:72113331..72115330,2	MCF-7	breast:
16	chr9:72089279..72091764-chr9:72373318..72374835,2	MCF-7	breast:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM189A2-3	chr9:72124873-72127579	ucscGeneNc_uc004ahs_1
2	lnc-FAM189A2-1	chr9:72109203-72109429	ENSG00000229312.1
3	lnc-FAM189A2-1	chr9:72109203-72109429	ENSG00000229312.2

No data

Variant related genes	Relation type
ENSG00000229312	chromatin interactions

Extended variants
information (count: 1469 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:1469 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2777864	chr9:72091413-72091414	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs555267616	chr9:72091431-72091432	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs576820303	chr9:72091535-72091536	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs183042985	chr9:72091541-72091542	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs141480676	chr9:72091546-72091547	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs12555572	chr9:72091547-72091548	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs573497290	chr9:72091588-72091589	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs565123900	chr9:72091598-72091599	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs190302462	chr9:72091631-72091632	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs541148397	chr9:72091680-72091681	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs114078700	chr9:72091685-72091686	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs144546752	chr9:72091686-72091687	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs541637348	chr9:72091759-72091760	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs79698967	chr9:72091791-72091792	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs2777865	chr9:72091799-72091800	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs148755018	chr9:72091801-72091802	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs563911327	chr9:72091802-72091803	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs528117370	chr9:72091861-72091862	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs144681679	chr9:72091885-72091886	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs182698286	chr9:72091888-72091889	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs536804753	chr9:72091905-72091906	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs187529242	chr9:72091910-72091911	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs370920464	chr9:72091911-72091912	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs10867620	chr9:72091929-72091930	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs192782560	chr9:72091938-72091939	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs559324620	chr9:72092024-72092025	Active TSS Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs577143832	chr9:72092027-72092028	Active TSS Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs114025313	chr9:72092029-72092030	Active TSS Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs574083964	chr9:72092030-72092031	Active TSS Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs10124725	chr9:72092061-72092062	Active TSS Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs574885110	chr9:72092067-72092068	Active TSS Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs10125397	chr9:72092079-72092080	Active TSS Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs386734790	chr9:72092084-72092085	Active TSS Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs12346899	chr9:72092086-72092087	Active TSS Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs575136896	chr9:72092089-72092090	Active TSS Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs12352610	chr9:72092126-72092127	Active TSS Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs564428397	chr9:72092165-72092166	Active TSS Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs12337530	chr9:72092185-72092186	Active TSS Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs10121657	chr9:72092191-72092192	Active TSS Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs10115310	chr9:72092196-72092197	Active TSS Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs13298819	chr9:72092214-72092215	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs561584302	chr9:72092231-72092232	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs528997655	chr9:72092266-72092267	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs13292735	chr9:72092273-72092274	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs28651251	chr9:72092280-72092281	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs570250027	chr9:72092309-72092310	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs368411033	chr9:72092318-72092319	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs571137640	chr9:72092319-72092320	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs72377303	chr9:72092331-72092332	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs199935564	chr9:72092342-72092343	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:61)

Disease	PMID	Source
Breast cancer	17133270	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Medulloblastoma	21979893	CNVD
microdeletion syndrome	16199537	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Urothelial carcinoma	21177765	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Melanoma	22183965	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	16751803	CNVD
Myelofibrosis	22110671	CNVD
lymphocytic leukemia	21291569	CNVD
Leukemia	17361228	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Glioblastoma	16823260	CNVD
Leukemia	18688285	CNVD
Non-small cell lung cancer	21044232	CNVD
Brain cancer	20823417	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Renal cell carcinoma	19461508	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Heart disease	21282601	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	17899364	CNVD
Mantle cell lymphoma	19029149	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute myeloid leukemia	20729466	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Oral cancer	21386901	CNVD
Epilepsy	22083797	CNVD
Glioblastoma multiforme	21750150	CNVD
Cancer	21183584	CNVD
Bipolar disorder	18458673	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:393 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:72079000-72091600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr9:72086600-72091800	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr9:72087600-72091600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr9:72087600-72091600	Weak transcription	HUES64 Cell Line	embryonic stem cell
5	chr9:72087800-72091600	Weak transcription	Rectal Mucosa Donor 29	rectum
6	chr9:72087800-72101400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr9:72088000-72096800	Weak transcription	Liver	Liver
8	chr9:72089000-72092200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
9	chr9:72089200-72091800	Enhancers	Primary T helper naive cells from peripheral blood	blood
10	chr9:72089200-72092000	Enhancers	Primary T helper cells fromperipheralblood	blood
11	chr9:72089400-72092000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
12	chr9:72089400-72092000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
13	chr9:72089400-72092200	Enhancers	Fetal Thymus	thymus
14	chr9:72089800-72091800	Enhancers	Brain Inferior Temporal Lobe	brain
15	chr9:72089800-72092000	Enhancers	Primary T helper cells PMA-I stimulated	--
16	chr9:72089800-72092000	Enhancers	Stomach Mucosa	stomach
17	chr9:72090000-72091800	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
18	chr9:72090200-72092000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
19	chr9:72090400-72091600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr9:72090400-72091800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
21	chr9:72090400-72092000	Enhancers	Breast Myoepithelial Primary Cells	Breast
22	chr9:72090600-72091600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
23	chr9:72090600-72091800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
24	chr9:72090800-72091800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
25	chr9:72090800-72091800	Weak transcription	Rectal Mucosa Donor 31	rectum
26	chr9:72091000-72091800	Enhancers	Cortex derived primary cultured neurospheres	brain
27	chr9:72091000-72092000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr9:72091000-72092000	Enhancers	Esophagus	oesophagus
29	chr9:72091000-72092000	Enhancers	Fetal Brain Female	brain
30	chr9:72091000-72092200	Enhancers	Primary T cells from cord blood	blood
31	chr9:72091200-72091600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
32	chr9:72091200-72091600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
33	chr9:72091400-72091600	Enhancers	ES-I3 Cell Line	embryonic stem cell
34	chr9:72091400-72091600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
35	chr9:72091400-72091600	Enhancers	iPS-15b Cell Line	embryonic stem cell
36	chr9:72091400-72091600	Enhancers	iPS-20b Cell Line	embryonic stem cell
37	chr9:72091400-72091800	Enhancers	Primary hematopoietic stem cells	blood
38	chr9:72091400-72091800	Enhancers	Brain Anterior Caudate	brain
39	chr9:72091400-72092000	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
40	chr9:72091400-72092000	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
41	chr9:72091400-72092000	Enhancers	iPS-18 Cell Line	embryonic stem cell
42	chr9:72091600-72091800	Enhancers	Primary hematopoietic stem cells short term culture	blood
43	chr9:72091600-72091800	Enhancers	Duodenum Mucosa	Duodenum
44	chr9:72091600-72092000	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
45	chr9:72091600-72092000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
46	chr9:72091600-72092000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
47	chr9:72091600-72092000	Enhancers	HUES64 Cell Line	embryonic stem cell
48	chr9:72091600-72092000	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
49	chr9:72091600-72092000	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
50	chr9:72091600-72092000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell

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