Variant report

Variant	nsv1018462
Chromosome Location	chr7:4097676-4173613
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:338)
CpG islands
(count:2260)
Chromatin interactive
region (count:12)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:338 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr7:4170503-4171267	H1-hESC	embryonic stem cell:	n/a	n/a
2	CBX3	chr7:4143342-4143771	K562	blood:	n/a	n/a
3	CEBPB	chr7:4133326-4133404	K562	blood:	n/a	n/a
4	CEBPB	chr7:4143725-4143868	HepG2	liver:	n/a	chr7:4143746-4143757
5	CEBPB	chr7:4143145-4143844	MCF-7	breast:	n/a	chr7:4143746-4143757
6	CEBPB	chr7:4164261-4164462	A549	lung:	n/a	chr7:4164348-4164359 chr7:4164347-4164358
7	CEBPB	chr7:4170662-4170944	H1-hESC	embryonic stem cell:	n/a	n/a
8	CEBPB	chr7:4164281-4164504	HepG2	liver:	n/a	chr7:4164348-4164359 chr7:4164347-4164358
9	CEBPB	chr7:4098994-4099005	IMR90	lung:	n/a	n/a
10	CEBPB	chr7:4143302-4143760	H1-hESC	embryonic stem cell:	n/a	chr7:4143746-4143757
11	CEBPB	chr7:4143283-4143797	A549	lung:	n/a	chr7:4143746-4143757
12	CEBPB	chr7:4133313-4133359	A549	lung:	n/a	n/a
13	CEBPB	chr7:4143335-4143889	K562	blood:	n/a	chr7:4143746-4143757
14	CEBPZ	chr7:4098999-4099105	HepG2	liver:	n/a	n/a
15	CHD2	chr7:4143451-4143520	K562	blood:	n/a	n/a
16	CREB1	chr7:4114732-4114984	A549	lung:	n/a	n/a
17	CTCF	chr7:4170780-4170930	HRPEpiC	eye:	n/a	n/a
18	CTCF	chr7:4143040-4143190	SK-N-SH_RA	brain:	n/a	chr7:4143161-4143179
19	CTCF	chr7:4170780-4170930	WERI-Rb-1	eye:	n/a	n/a
20	CTCF	chr7:4170760-4170910	SK-N-SH_RA	brain:	n/a	n/a
21	CTCF	chr7:4114720-4114870	WERI-Rb-1	eye:	n/a	chr7:4114833-4114842
22	CTCF	chr7:4143025-4143288	HepG2	liver:	n/a	chr7:4143161-4143179
23	CTCF	chr7:4170846-4170874	MCF-7	breast:	n/a	n/a
24	CTCF	chr7:4143019-4143302	K562	blood:	n/a	chr7:4143161-4143179
25	CTCF	chr7:4142940-4143090	HEK293	kidney:	n/a	n/a
26	CTCF	chr7:4143080-4143230	HCT-116	colon:	n/a	chr7:4143161-4143179
27	CTCF	chr7:4143160-4143310	MCF-7	breast:	n/a	chr7:4143161-4143179
28	CTCF	chr7:4143100-4143250	RPTEC	kidney:	n/a	chr7:4143161-4143179
29	CTCF	chr7:4142417-4142435	Spleen_OC	spleen:	n/a	n/a
30	CTCF	chr7:4143060-4143210	HCFaa	heart:	n/a	chr7:4143161-4143179
31	CTCF	chr7:4143060-4143210	HBMEC	blood vessel:	n/a	chr7:4143161-4143179
32	CTCF	chr7:4143060-4143210	HA-sp	spinal cord:	n/a	chr7:4143161-4143179
33	CTCF	chr7:4143381-4143421	NHEK	skin:	n/a	n/a
34	CTCF	chr7:4143109-4143186	Spleen_OC	spleen:	n/a	chr7:4143161-4143179
35	CTCF	chr7:4114673-4114817	HepG2	liver:	n/a	n/a
36	CTCF	chr7:4134769-4134868	GM10248	blood:	n/a	n/a
37	CTCF	chr7:4143060-4143210	HMF	breast:	n/a	chr7:4143161-4143179
38	CTCF	chr7:4143400-4143550	SK-N-SH_RA	brain:	n/a	n/a
39	CTCF	chr7:4143120-4143270	HPAF	blood vessel:	n/a	chr7:4143161-4143179
40	CTCF	chr7:4120669-4120793	K562	blood:	n/a	n/a
41	CTCF	chr7:4143120-4143270	HCT-116	colon:	n/a	chr7:4143161-4143179
42	CTCF	chr7:4114715-4114809	HepG2	liver:	n/a	n/a
43	CTCF	chr7:4169540-4169690	Hela-S3	cervix:	n/a	n/a
44	CTCF	chr7:4120800-4120950	GM12865	blood:	n/a	n/a
45	CTCF	chr7:4114660-4114810	WERI-Rb-1	eye:	n/a	n/a
46	CTCF	chr7:4114640-4114790	SK-N-SH_RA	brain:	n/a	n/a
47	CTCF	chr7:4169540-4169690	K562	blood:	n/a	n/a
48	CTCF	chr7:4142020-4142170	HepG2	liver:	n/a	n/a
49	CTCF	chr7:4143007-4143365	K562	blood:	n/a	chr7:4143161-4143179
50	CTCF	chr7:4142940-4143090	HRE	kidney:	n/a	n/a

(count:2260 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:4150753-4150803	RPTEC	kidney:	n/a
2	chr7:4169752-4169802	HRE	kidney:	n/a
3	chr7:4153707-4153757	Jurkat	blood:	n/a
4	chr7:4150753-4150803	RPTEC	kidney:	n/a
5	chr7:4169752-4169802	HRE	kidney:	n/a
6	chr7:4153707-4153757	Jurkat	blood:	n/a
7	chr7:4168039-4168089	HL-60	blood:	n/a
8	chr7:4167607-4167657	AG09309	skin:	n/a
9	chr7:4168039-4168089	U87	brain:	n/a
10	chr7:4169604-4169654	AG04450	lung:	fetal
11	chr7:4133359-4133409	HRPEpiC	eye:	n/a
12	chr7:4118583-4118633	HCT-116	colon:	n/a
13	chr7:4118868-4118918	GM12878	blood:	n/a
14	chr7:4147330-4147380	HIPEpiC	eye:	n/a
15	chr7:4119142-4119192	RPTEC	kidney:	n/a
16	chr7:4169604-4169654	NHBE	bronchial:	n/a
17	chr7:4146971-4147021	NHDF-neo	bronchial:	n/a
18	chr7:4153868-4153918	PANC-1	pancreas:	n/a
19	chr7:4169314-4169364	SK-N-SH	brain:	n/a
20	chr7:4146291-4146341	AG10803	skin:	n/a
21	chr7:4172065-4172115	MCF-7	breast:	n/a
22	chr7:4146291-4146341	HNPCEpiC	eye:	n/a
23	chr7:4118825-4118875	HEEpiC	esophagus:	n/a
24	chr7:4169314-4169364	A549	lung:	n/a
25	chr7:4146971-4147021	ovcar-3	ovarian:	n/a
26	chr7:4167607-4167657	BJ	skin:	n/a
27	chr7:4119142-4119192	Hepatocyte	liver:	n/a
28	chr7:4167943-4167993	IMR90	lung:	fetal
29	chr7:4167809-4167859	T-47D	breast:	n/a
30	chr7:4153732-4153782	AG09319	gingival:	n/a
31	chr7:4153767-4153817	HL-60	blood:	n/a
32	chr7:4118609-4118659	HCM	heart:	n/a
33	chr7:4118583-4118633	PFSK-1	brain:	n/a
34	chr7:4118583-4118633	HepG2	liver:	n/a
35	chr7:4152953-4153003	RPTEC	kidney:	n/a
36	chr7:4169630-4169680	HMEC	breast:	n/a
37	chr7:4152953-4153003	NHBE	bronchial:	n/a
38	chr7:4172065-4172115	AG04450	lung:	fetal
39	chr7:4169752-4169802	HCT-116	colon:	n/a
40	chr7:4153919-4153969	MCF10A-Er-Src	breast:	n/a
41	chr7:4152976-4153026	HCM	heart:	n/a
42	chr7:4113480-4113530	GM12891	blood:	n/a
43	chr7:4169752-4169802	IMR90	lung:	fetal
44	chr7:4147432-4147482	NHBE	bronchial:	n/a
45	chr7:4153767-4153817	GM19239	blood:	n/a
46	chr7:4118609-4118659	SK-N-SH_RA	brain:	n/a
47	chr7:4152953-4153003	IMR90	lung:	fetal
48	chr7:4169306-4169356	HIPEpiC	eye:	n/a
49	chr7:4146291-4146341	ovcar-3	ovarian:	n/a
50	chr7:4167809-4167859	ECC-1	luminal epithelium:	n/a

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:4149016..4150999-chr7:4154652..4156380,2	K562	blood:
2	chr7:4126299..4129076-chr7:4130764..4133447,2	K562	blood:
3	chr7:4159770..4161422-chr7:4162793..4165151,2	K562	blood:
4	chr7:4171607..4173163-chr7:4322084..4324253,2	K562	blood:
5	chr7:4133522..4135936-chr7:4136765..4138658,2	K562	blood:
6	chr7:4149016..4150999-chr7:4154652..4156380,2	K562	blood:
7	chr7:4143002..4143685-chr7:4518859..4519662,3	MCF-7	breast:
8	chr7:4133522..4135936-chr7:4136765..4138658,2	K562	blood:
9	chr7:4159770..4161422-chr7:4162793..4165151,2	K562	blood:
10	chr7:4130773..4135650-chr7:4142053..4144303,4	MCF-7	breast:
11	chr7:4126299..4129076-chr7:4130764..4133447,2	K562	blood:
12	chr7:4130773..4135650-chr7:4142053..4144303,4	MCF-7	breast:

No data

Variant related genes	Relation type
SDK1	TF binding region
SDK1	CpG island

Extended variants
information (count: 4357 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:4357 , 50 per page) page: 1 2 3 4 5 6 7 ... 88

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6462570	chr7:4097676-4097677	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs574377061	chr7:4097682-4097683	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs543022593	chr7:4097707-4097708	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs563057182	chr7:4097708-4097709	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs59085880	chr7:4097721-4097722	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs532060753	chr7:4097734-4097735	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs545222193	chr7:4097779-4097780	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs372193988	chr7:4097816-4097817	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs527843181	chr7:4097823-4097824	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs181102066	chr7:4097846-4097847	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs6462571	chr7:4097856-4097857	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs35564659	chr7:4097885-4097886	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs530124317	chr7:4097914-4097915	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs369016188	chr7:4097916-4097917	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs549893066	chr7:4097945-4097946	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs542951680	chr7:4097969-4097970	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs570192725	chr7:4098004-4098005	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs539131684	chr7:4098034-4098035	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs77295490	chr7:4098049-4098050	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs565889782	chr7:4098087-4098088	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs534471621	chr7:4098101-4098102	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs373335044	chr7:4098105-4098106	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs570090606	chr7:4098116-4098117	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs149273773	chr7:4098133-4098134	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs574608946	chr7:4098209-4098210	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs185602338	chr7:4098231-4098232	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs188108064	chr7:4098241-4098242	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs576573593	chr7:4098260-4098261	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs545482138	chr7:4098264-4098265	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs558979305	chr7:4098276-4098277	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs180690164	chr7:4098281-4098282	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs576177549	chr7:4098296-4098297	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs541234255	chr7:4098347-4098348	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs147376007	chr7:4098390-4098391	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs117780330	chr7:4098424-4098425	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs185998714	chr7:4098444-4098445	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs137952184	chr7:4098512-4098513	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs563664161	chr7:4098525-4098526	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs113739730	chr7:4098539-4098540	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs552707314	chr7:4098588-4098589	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs566011526	chr7:4098607-4098608	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs79015390	chr7:4098653-4098654	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs548063761	chr7:4098667-4098668	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs192160194	chr7:4098672-4098673	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs143394253	chr7:4098677-4098678	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs1080840	chr7:4098699-4098700	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs556577098	chr7:4098716-4098717	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs534857241	chr7:4098757-4098758	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs576436387	chr7:4098763-4098764	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs112774955	chr7:4098779-4098780	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:81)

Disease	PMID	Source
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Chordoma	21602918	CNVD
Lynch syndrome	22585707	CNVD
Follicular lymphoma	20505157	CNVD
Breast cancer	16397240	CNVD
Raine Syndrome	17924334	CNVD
Diffuse large b-cell lymphoma	21266526	CNVD
Melanoma	18172304	CNVD
Sudden cardiac death	19188705	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Glioma	18556773	CNVD
Ovarian cancer	21720365	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Ovarian cancer	22174824	CNVD
Urothelial carcinoma	18382360	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Biliary cancer	19435499	CNVD
Cancer	16751803	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
colon cancer	17210682	CNVD
Lung adenocarcinoma	21810691	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Colorectal cancer	19359472	CNVD
Hypothalamic hamartomas	18252217	CNVD
Human rectal carcinomas	16397240	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Medulloblastoma	18056178	CNVD
Basal cell lymphoma	17170743	CNVD
Ewing''s sarcoma	21437220	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Developmental delay	21147756	CNVD
Prostate cancer	18632612	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
Spondylocostal dysostosis	21085971	CNVD
Mental retardation	17901693	CNVD
Heart disease	21282601	CNVD
Glioblastoma multiforme	22286061	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	17053054	CNVD
Cancer	20164920	CNVD
Colorectal cancer	21645411	CNVD
Intellectual disability	21811512	CNVD
Breast cancer	22522925	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Urothelial carcinoma	21177765	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:647 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:4087600-4111800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr7:4088800-4129400	Weak transcription	Right Ventricle	heart
3	chr7:4093200-4104400	Weak transcription	Fetal Stomach	stomach
4	chr7:4093800-4097800	Weak transcription	Pancreatic Islets	Pancreatic Islet
5	chr7:4095200-4104800	Weak transcription	Cortex derived primary cultured neurospheres	brain
6	chr7:4096000-4116400	Weak transcription	Adipose Nuclei	Adipose
7	chr7:4096800-4098200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
8	chr7:4097200-4110000	Weak transcription	Gastric	stomach
9	chr7:4097400-4097800	Weak transcription	Fetal Lung	lung
10	chr7:4097400-4098000	Weak transcription	Spleen	Spleen
11	chr7:4097400-4105800	Weak transcription	Aorta	Aorta
12	chr7:4097400-4106000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr7:4097400-4106800	Weak transcription	Pancreas	Pancrea
14	chr7:4097400-4108800	Weak transcription	Fetal Intestine Small	intestine
15	chr7:4097400-4109000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr7:4097400-4109400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr7:4097800-4098000	ZNF genes & repeats	Fetal Lung	lung
18	chr7:4097800-4098200	Enhancers	Muscle Satellite Cultured Cells	--
19	chr7:4098200-4098400	Weak transcription	Fetal Lung	lung
20	chr7:4098200-4104800	Weak transcription	Muscle Satellite Cultured Cells	--
21	chr7:4098600-4099000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
22	chr7:4103000-4125600	Weak transcription	Pancreatic Islets	Pancreatic Islet
23	chr7:4103200-4106000	Weak transcription	Spleen	Spleen
24	chr7:4104400-4105200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
25	chr7:4104400-4105200	Enhancers	Fetal Stomach	stomach
26	chr7:4104600-4104800	Enhancers	Primary neutrophils fromperipheralblood	blood
27	chr7:4104600-4104800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr7:4104600-4105000	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr7:4104600-4105000	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
30	chr7:4104600-4105000	Enhancers	Fetal Lung	lung
31	chr7:4104600-4105200	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr7:4104600-4105200	Enhancers	Colon Smooth Muscle	Colon
33	chr7:4104800-4105000	Enhancers	Breast Myoepithelial Primary Cells	Breast
34	chr7:4104800-4105000	Enhancers	Cortex derived primary cultured neurospheres	brain
35	chr7:4104800-4105200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr7:4104800-4105200	Enhancers	Muscle Satellite Cultured Cells	--
37	chr7:4104800-4105200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
38	chr7:4104800-4116400	Weak transcription	Primary neutrophils fromperipheralblood	blood
39	chr7:4105000-4105200	Enhancers	Fetal Brain Male	brain
40	chr7:4105000-4105400	Weak transcription	Cortex derived primary cultured neurospheres	brain
41	chr7:4105000-4106200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
42	chr7:4105000-4109200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
43	chr7:4105200-4106400	Weak transcription	Colon Smooth Muscle	Colon
44	chr7:4105200-4106600	Weak transcription	Fetal Brain Male	brain
45	chr7:4105200-4109000	Weak transcription	Fetal Stomach	stomach
46	chr7:4105200-4111000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
47	chr7:4105200-4117000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr7:4105200-4120200	Weak transcription	Muscle Satellite Cultured Cells	--
49	chr7:4105400-4105600	Enhancers	Cortex derived primary cultured neurospheres	brain
50	chr7:4105600-4111000	Weak transcription	Cortex derived primary cultured neurospheres	brain

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