Variant report

Variant	esv19421
Chromosome Location	chr9:97068893-97089175
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr9:97064666..97066438-chr9:97068084..97069601,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF169-1	chr9:97076744-97076871	XLOC_007467
2	lnc-ZNF169-1	chr9:97075822-97075909	XLOC_007467

Extended variants
information (count: 303 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:303 , 50 per page) page: 1 2 3 4 5 6 7

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs576150389	chr9:97076766-97076767	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
2	rs55639420	chr9:97076813-97076814	Inactive region	lncRNA	n/a	Overlapped CNVs	mRNA abundance
3	rs75933910	chr9:97076814-97076815	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
4	rs7026729	chr9:97083206-97083207	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs182051654	chr9:97083216-97083217	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs148461503	chr9:97083221-97083222	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs530499022	chr9:97083242-97083243	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs533805171	chr9:97083245-97083246	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs548636758	chr9:97083250-97083251	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs555165892	chr9:97083302-97083303	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs573735635	chr9:97083336-97083337	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs543984347	chr9:97083397-97083398	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs556214378	chr9:97083422-97083423	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs577612544	chr9:97083428-97083429	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs567362265	chr9:97083479-97083480	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs370198532	chr9:97083486-97083487	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs535474674	chr9:97083495-97083496	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs545000710	chr9:97083505-97083506	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs560802376	chr9:97083514-97083515	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs201933017	chr9:97083518-97083519	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs543314392	chr9:97083566-97083567	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs187102839	chr9:97083567-97083568	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs531891891	chr9:97083585-97083586	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs550044555	chr9:97083614-97083615	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs571707947	chr9:97083616-97083617	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs191483725	chr9:97083617-97083618	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs183547293	chr9:97083625-97083626	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs547368931	chr9:97083641-97083642	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs546581312	chr9:97083654-97083655	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs565711190	chr9:97083702-97083703	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs533841029	chr9:97083703-97083704	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs555204587	chr9:97083717-97083718	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs567390650	chr9:97083721-97083722	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs369639680	chr9:97083751-97083752	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs538042027	chr9:97083775-97083776	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs556014876	chr9:97083804-97083805	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs577651971	chr9:97083805-97083806	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs545089810	chr9:97083815-97083816	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs553823757	chr9:97083868-97083869	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs572024399	chr9:97083916-97083917	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs543351572	chr9:97083920-97083921	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs571513335	chr9:97083924-97083925	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs561614856	chr9:97084011-97084012	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs531855239	chr9:97084053-97084054	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs543971842	chr9:97084086-97084087	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs78953266	chr9:97084115-97084116	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs532493599	chr9:97084124-97084125	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs547442188	chr9:97084143-97084144	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs2479583	chr9:97084165-97084166	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs185519961	chr9:97084174-97084175	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:78)

Disease	PMID	Source
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
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
Hodgkin''s lymphoma	17606441	CNVD
Acute myeloid leukemia	21251322	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral cancer	21386901	CNVD
Bipolar disorder	18458673	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Wilms tumour	21544195	CNVD
Prostate cancer	18632612	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Gastric cancer	17908304	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Biliary cancer	19435499	CNVD
small cell lung cancer	20016488	CNVD
Intracranial aneurysm	16715129	CNVD
Cardiac fibroma	18329553	CNVD
Breast cancer	17133270	CNVD
Basal cell nevus syndrome	21572526	CNVD
Mental retardation	19951919	CNVD
Retinoblastoma	22278416	CNVD
9q22.3 microdeletion syndrome	22283845	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Microcephaly	18830227	CNVD
overgrowth syndrome	16570072	CNVD
Effusion lymphoma	18079361	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:97083200-97094600	Weak transcription	Right Atrium	heart
2	chr9:97084600-97085000	Enhancers	K562	blood
3	chr9:97084600-97086000	Active TSS	HepG2	liver
4	chr9:97086000-97086200	Flanking Active TSS	HepG2	liver
5	chr9:97086200-97086800	Enhancers	HepG2	liver
6	chr9:97086800-97088000	Weak transcription	HepG2	liver
7	chr9:97088000-97088400	Active TSS	HepG2	liver
8	chr9:97088000-97089200	Enhancers	Primary neutrophils fromperipheralblood	blood
9	chr9:97089000-97089200	Enhancers	Primary B cells from peripheral blood	blood

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