Variant report

Variant	nsv613204
Chromosome Location	chr9:5931216-5971977
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:5953963-5954043	K562	blood:	n/a	n/a
2	BATF	chr9:5958310-5958603	GM12878	blood:	n/a	n/a
3	BATF	chr9:5951684-5952012	GM12878	blood:	n/a	n/a
4	BATF	chr9:5951664-5951938	GM12878	blood:	n/a	n/a
5	BCL11A	chr9:5945117-5945389	GM12878	blood:	n/a	n/a
6	BCLAF1	chr9:5958212-5958712	GM12878	blood:	n/a	chr9:5958372-5958381
7	BHLHE40	chr9:5949182-5949457	GM12878	blood:	n/a	n/a
8	BHLHE40	chr9:5947802-5948113	GM12878	blood:	n/a	n/a
9	BHLHE40	chr9:5958429-5958517	GM12878	blood:	n/a	n/a
10	BHLHE40	chr9:5947846-5948136	K562	blood:	n/a	n/a
11	BRCA1	chr9:5943893-5943913	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr9:5953772-5953989	K562	blood:	n/a	chr9:5953829-5953838 chr9:5953828-5953839 chr9:5953829-5953838
13	CEBPB	chr9:5957409-5957411	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr9:5949182-5949463	MCF-7	breast:	n/a	n/a
15	CEBPB	chr9:5949112-5949654	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr9:5949233-5949451	A549	lung:	n/a	n/a
17	CEBPB	chr9:5952747-5952878	H1-hESC	embryonic stem cell:	n/a	chr9:5952803-5952814
18	CEBPB	chr9:5938587-5938830	A549	lung:	n/a	chr9:5938675-5938686 chr9:5938674-5938687 chr9:5938676-5938685
19	CEBPB	chr9:5938646-5938749	K562	blood:	n/a	chr9:5938675-5938686 chr9:5938674-5938687 chr9:5938676-5938685
20	CEBPB	chr9:5952644-5952960	IMR90	lung:	n/a	chr9:5952803-5952814
21	CEBPB	chr9:5952624-5952924	A549	lung:	n/a	chr9:5952803-5952814
22	CEBPB	chr9:5952703-5952903	K562	blood:	n/a	chr9:5952803-5952814
23	CEBPB	chr9:5938531-5938843	IMR90	lung:	n/a	chr9:5938675-5938686 chr9:5938674-5938687 chr9:5938676-5938685
24	CEBPB	chr9:5953664-5954018	K562	blood:	n/a	chr9:5953829-5953838 chr9:5953828-5953839 chr9:5953829-5953838
25	CEBPB	chr9:5938528-5938821	HepG2	liver:	n/a	chr9:5938675-5938686 chr9:5938674-5938687 chr9:5938676-5938685
26	CEBPB	chr9:5953768-5953974	IMR90	lung:	n/a	chr9:5953829-5953838 chr9:5953828-5953839 chr9:5953829-5953838
27	CEBPB	chr9:5952658-5952962	HepG2	liver:	n/a	chr9:5952803-5952814
28	CEBPB	chr9:5953808-5954004	A549	lung:	n/a	chr9:5953829-5953838 chr9:5953828-5953839 chr9:5953829-5953838
29	CEBPB	chr9:5953759-5953990	HepG2	liver:	n/a	chr9:5953829-5953838 chr9:5953828-5953839 chr9:5953829-5953838
30	CHD2	chr9:5958298-5958498	GM12878	blood:	n/a	n/a
31	CHD2	chr9:5947844-5948241	GM12878	blood:	n/a	n/a
32	CTCF	chr9:5969585-5969655	Medullo	brain:	n/a	n/a
33	CTCF	chr9:5949480-5949630	HMF	breast:	n/a	n/a
34	CTCF	chr9:5966585-5966639	GM13977	blood:	n/a	n/a
35	E2F4	chr9:5946033-5946225	MCF10A-Er-Src	breast:	n/a	n/a
36	E2F4	chr9:5961492-5961657	MCF10A-Er-Src	breast:	n/a	n/a
37	E2F4	chr9:5951556-5951916	MCF10A-Er-Src	breast:	n/a	n/a
38	EBF1	chr9:5951821-5951941	GM12878	blood:	n/a	n/a
39	ELF1	chr9:5949111-5949477	SK-N-SH	brain:	n/a	chr9:5949277-5949290
40	ELF1	chr9:5948994-5949499	SK-N-SH	brain:	n/a	chr9:5949277-5949290
41	ELF1	chr9:5949091-5949414	GM12878	blood:	n/a	chr9:5949277-5949290
42	ELF1	chr9:5949200-5949392	K562	blood:	n/a	chr9:5949277-5949290
43	ELF1	chr9:5949095-5949389	A549	lung:	n/a	chr9:5949277-5949290
44	ELF1	chr9:5949004-5949569	MCF-7	breast:	n/a	chr9:5949277-5949290
45	EP300	chr9:5958242-5958573	GM12878	blood:	n/a	chr9:5958386-5958400 chr9:5958372-5958386
46	EP300	chr9:5947852-5948136	GM12878	blood:	n/a	chr9:5948072-5948085
47	EP300	chr9:5941286-5941343	GM12878	blood:	n/a	n/a
48	EP300	chr9:5945105-5945497	GM12878	blood:	n/a	n/a
49	EP300	chr9:5947890-5948016	K562	blood:	n/a	n/a
50	EP300	chr9:5958267-5958502	GM12878	blood:	n/a	chr9:5958386-5958400 chr9:5958372-5958386

No.	Distal block	Cell Line	Cell type
1	chr9:5943208..5945501-chr9:5954094..5957018,2	K562	blood:
2	chr9:5967488..5970171-chr9:6006384..6008559,2	K562	blood:
3	chr9:5913974..5916739-chr9:5930124..5932087,2	K562	blood:
4	chr9:5957297..5958890-chr9:6003924..6006485,2	K562	blood:
5	chr9:5943208..5945501-chr9:5954094..5957018,2	K562	blood:
6	chr9:5941718..5944102-chr9:5948002..5951103,3	K562	blood:
7	chr9:5952476..5954023-chr9:5957986..5959707,2	K562	blood:
8	chr9:5950623..5953184-chr9:5954140..5956964,2	K562	blood:
9	chr9:5942732..5945231-chr9:5951340..5953826,2	K562	blood:
10	chr9:5928321..5930206-chr9:5944196..5946091,2	K562	blood:
11	chr9:5937769..5939374-chr9:5940961..5942645,2	MCF-7	breast:
12	chr9:5947429..5950092-chr9:5954618..5958413,3	K562	blood:
13	chr9:5942732..5945231-chr9:5951340..5953826,2	K562	blood:
14	chr9:5947429..5950092-chr9:5954618..5958413,3	K562	blood:
15	chr9:5950623..5953184-chr9:5954140..5956964,2	K562	blood:
16	chr9:5941718..5944102-chr9:5948002..5951103,3	K562	blood:
17	chr9:5924252..5926200-chr9:5929178..5931447,2	MCF-7	breast:
18	chr9:5952476..5954023-chr9:5957986..5959707,2	K562	blood:
19	chr9:5940164..5943211-chr9:5943704..5946598,3	K562	blood:
20	chr9:5925409..5927394-chr9:5940520..5942739,2	MCF-7	breast:
21	chr9:5937769..5939374-chr9:5940961..5942645,2	MCF-7	breast:
22	chr9:5930058..5932668-chr9:5946497..5948957,2	K562	blood:
23	chr9:5930058..5932668-chr9:5946497..5948957,2	K562	blood:
24	chr9:5940164..5943211-chr9:5943704..5946598,3	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RANBP6-1	chr9:5936604-5936948	NONHSAT130120

Variant related genes	Relation type
KIAA2026	TF binding region
ENSG00000263575	chromatin interactions
ENSG00000183354	chromatin interactions

Extended variants
information (count: 1720 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:1720 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1478938	chr9:5931216-5931217	Weak transcription Genic enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs571343177	chr9:5931222-5931223	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs372676870	chr9:5931306-5931307	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs183046292	chr9:5931326-5931327	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs550635601	chr9:5931364-5931365	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs568789936	chr9:5931365-5931366	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs148186486	chr9:5931490-5931491	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs548542782	chr9:5931520-5931521	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs185174811	chr9:5931528-5931529	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs566730349	chr9:5931537-5931538	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs141159804	chr9:5931587-5931588	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs558438752	chr9:5931606-5931607	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs189935539	chr9:5931609-5931610	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs182390590	chr9:5931635-5931636	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs187829911	chr9:5931656-5931657	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs192641722	chr9:5931684-5931685	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs574537590	chr9:5931706-5931707	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs183654496	chr9:5931725-5931726	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs560372068	chr9:5931733-5931734	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs10975353	chr9:5931790-5931791	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs572378881	chr9:5931815-5931816	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs546004229	chr9:5931875-5931876	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs564558949	chr9:5931898-5931899	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs548605761	chr9:5931902-5931903	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs552295047	chr9:5931909-5931910	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs188377534	chr9:5931926-5931927	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs562592779	chr9:5932027-5932028	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs10975354	chr9:5932043-5932044	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs548161000	chr9:5932119-5932120	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs566793593	chr9:5932152-5932153	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs10975355	chr9:5932157-5932158	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs75054295	chr9:5932184-5932185	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs373634598	chr9:5932246-5932247	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs562327361	chr9:5932248-5932249	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs530942381	chr9:5932252-5932253	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs538039899	chr9:5932254-5932255	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs556393250	chr9:5932261-5932262	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs574547724	chr9:5932297-5932298	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs146193374	chr9:5932311-5932312	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs192827823	chr9:5932374-5932375	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs572092289	chr9:5932380-5932381	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs139178777	chr9:5932387-5932388	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs550966185	chr9:5932402-5932403	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs564800002	chr9:5932403-5932404	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs537060772	chr9:5932405-5932406	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs376464386	chr9:5932486-5932487	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs184874270	chr9:5932522-5932523	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs543953483	chr9:5932528-5932529	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs547831317	chr9:5932542-5932543	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs62554991	chr9:5932556-5932557	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:101)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Intracranial aneurysm	16715129	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Disorders of sex development	22290220	CNVD
Glioblastoma multiforme	21080181	CNVD
Sudden cardiac death	19188705	CNVD
Non-small cell lung cancer	21829676	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21183584	CNVD
Non-small cell lung cancer	21952639	CNVD
Disorders of sex development	21048976	CNVD
Neuroblastoma	18923191	CNVD
Intellectual disability	22102821	CNVD
abnormal development	18461090	CNVD
Honadal dysgenesis	21048976	CNVD
Medulloblastoma	21979893	CNVD
Lung cancer	16740712	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	16608533	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Cervical cancer	21063398	CNVD
Retinoblastoma	22278416	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Melanoma	18172304	CNVD
Biliary cancer	19435499	CNVD
Gastric cancer	21586687	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myopathy	18421352	CNVD
Neuroblastoma	18664255	CNVD
Acute lymphoblastic leukemia	18957548	CNVD
Myeloproliferative neoplasm	17564968	CNVD
Malignant meningioma	17937814	CNVD
Glioma	21971842	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oligodendroglial tumors	17285580	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
microdeletion syndrome	16199537	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Cancer	20164919	CNVD
Chronic myeloid leukemia	21384125	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Developmental delay	21147756	CNVD
Lung cancer	18438408	CNVD
XY gonadal dysgenesis	20685758	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Myelodysplastic syndrome	21251322	CNVD
Breast cancer	21785460	CNVD
Prostate cancer	18632612	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21858162	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Myelofibrosis	22110671	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Hepatocellular carcinoma	18803288	CNVD
Metastatic melanoma	18483359	CNVD
Glioblastoma	19074898	CNVD
Malignant melanoma	19074898	CNVD
Prostate cancer	16573809	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD

Chromatin state (count:681 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:5898400-5947200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
2	chr9:5919000-5939800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr9:5919800-5935600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
4	chr9:5920800-5938800	Weak transcription	Small Intestine	intestine
5	chr9:5921200-5939800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
6	chr9:5921200-5950400	Weak transcription	Psoas Muscle	Psoas
7	chr9:5922000-5941600	Weak transcription	HSMMtube	muscle
8	chr9:5922200-5935800	Weak transcription	Colon Smooth Muscle	Colon
9	chr9:5922400-5933400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
10	chr9:5922400-5935000	Weak transcription	Pancreas	Pancrea
11	chr9:5922400-5935200	Weak transcription	HMEC	breast
12	chr9:5922400-5939800	Weak transcription	Gastric	stomach
13	chr9:5922600-5947000	Weak transcription	Fetal Heart	heart
14	chr9:5923000-5936200	Weak transcription	Muscle Satellite Cultured Cells	--
15	chr9:5923000-5945200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
16	chr9:5923000-5969000	Weak transcription	Fetal Stomach	stomach
17	chr9:5923200-5933400	Weak transcription	Left Ventricle	heart
18	chr9:5923200-5933600	Weak transcription	Fetal Lung	lung
19	chr9:5923200-5934000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
20	chr9:5923200-5934200	Weak transcription	Colonic Mucosa	Colon
21	chr9:5923200-5934800	Weak transcription	Dnd41	blood
22	chr9:5923200-5935000	Weak transcription	Spleen	Spleen
23	chr9:5923200-5935000	Weak transcription	HepG2	liver
24	chr9:5923200-5935200	Weak transcription	Skeletal Muscle Male	skeletal muscle
25	chr9:5923200-5935800	Weak transcription	HUVEC	blood vessel
26	chr9:5923200-5938800	Weak transcription	Right Ventricle	heart
27	chr9:5923200-5939000	Weak transcription	Lung	lung
28	chr9:5923200-5939600	Weak transcription	Brain Angular Gyrus	brain
29	chr9:5923200-5943000	Weak transcription	Esophagus	oesophagus
30	chr9:5923200-5947600	Weak transcription	Fetal Kidney	kidney
31	chr9:5923200-5949200	Weak transcription	NHLF	lung
32	chr9:5923200-5968200	Weak transcription	Fetal Muscle Leg	muscle
33	chr9:5923200-5971800	Weak transcription	NHEK	skin
34	chr9:5923200-5972400	Weak transcription	Aorta	Aorta
35	chr9:5923400-5931600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
36	chr9:5923400-5933400	Weak transcription	Thymus	Thymus
37	chr9:5923400-5935800	Weak transcription	HUES6 Cell Line	embryonic stem cell
38	chr9:5923400-5939400	Weak transcription	Brain Inferior Temporal Lobe	brain
39	chr9:5923400-5939600	Weak transcription	Brain Cingulate Gyrus	brain
40	chr9:5924400-5935200	Weak transcription	Fetal Thymus	thymus
41	chr9:5924400-5935600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
42	chr9:5924600-5931800	Weak transcription	Rectal Mucosa Donor 29	rectum
43	chr9:5924600-5935600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
44	chr9:5924600-5939600	Weak transcription	Brain Hippocampus Middle	brain
45	chr9:5924600-5942600	Weak transcription	Brain Germinal Matrix	brain
46	chr9:5924600-5945200	Weak transcription	HUES64 Cell Line	embryonic stem cell
47	chr9:5924600-5946800	Weak transcription	Brain Substantia Nigra	brain
48	chr9:5924600-5949200	Weak transcription	Skeletal Muscle Female	skeletal muscle
49	chr9:5924600-5967400	Weak transcription	Brain Anterior Caudate	brain
50	chr9:5924600-5968600	Weak transcription	Cortex derived primary cultured neurospheres	brain

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