Variant report

Variant	nsv889966
Chromosome Location	chr8:4556264-4666654
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:178)
CpG islands
(count:610)
Chromatin interactive
region (count:4)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:178 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr8:4593306-4593480	K562	blood:	n/a	n/a
2	CEBPB	chr8:4613708-4613813	A549	lung:	n/a	n/a
3	CHD2	chr8:4644622-4644850	H1-hESC	embryonic stem cell:	n/a	n/a
4	CHD2	chr8:4654890-4654920	HepG2	liver:	n/a	n/a
5	CTBP2	chr8:4573370-4573868	H1-hESC	embryonic stem cell:	n/a	n/a
6	CTCF	chr8:4644640-4644790	GM12868	blood:	n/a	n/a
7	CTCF	chr8:4644640-4644790	HepG2	liver:	n/a	n/a
8	CTCF	chr8:4644640-4644790	GM12865	blood:	n/a	n/a
9	CTCF	chr8:4644660-4644810	HepG2	liver:	n/a	n/a
10	CTCF	chr8:4644540-4644690	HFF-Myc	foreskin:	n/a	n/a
11	CTCF	chr8:4644660-4644810	K562	blood:	n/a	n/a
12	CTCF	chr8:4644600-4644750	GM12872	blood:	n/a	n/a
13	CTCF	chr8:4644600-4644750	GM12871	blood:	n/a	n/a
14	CTCF	chr8:4644591-4644910	K562	blood:	n/a	n/a
15	CTCF	chr8:4650026-4650077	ProgFib	skin:	n/a	n/a
16	CTCF	chr8:4644660-4644810	GM12866	blood:	n/a	n/a
17	CTCF	chr8:4644600-4644750	WERI-Rb-1	eye:	n/a	n/a
18	CTCF	chr8:4644551-4644864	K562	blood:	n/a	n/a
19	CTCF	chr8:4644660-4644810	GM12868	blood:	n/a	n/a
20	CTCF	chr8:4644660-4644810	GM12864	blood:	n/a	n/a
21	CTCF	chr8:4644646-4644815	A549	lung:	n/a	n/a
22	CTCF	chr8:4644660-4644810	Hela-S3	cervix:	n/a	n/a
23	CTCF	chr8:4644700-4644850	Caco-2	colon:	n/a	n/a
24	CTCF	chr8:4644640-4644790	SK-N-SH_RA	brain:	n/a	n/a
25	CTCF	chr8:4644680-4644830	GM12871	blood:	n/a	n/a
26	CTCF	chr8:4573639-4573761	H1-hESC	embryonic stem cell:	n/a	n/a
27	CTCF	chr8:4628455-4628505	LNCaP	prostate:	n/a	n/a
28	CTCF	chr8:4644660-4644810	GM12865	blood:	n/a	n/a
29	CTCF	chr8:4644600-4644750	GM12873	blood:	n/a	n/a
30	CTCF	chr8:4644700-4644850	HRE	kidney:	n/a	n/a
31	CTCF	chr8:4644580-4644730	A549	lung:	n/a	n/a
32	CTCF	chr8:4644600-4644750	GM12864	blood:	n/a	n/a
33	CTCF	chr8:4644650-4644795	LNCaP	prostate:	n/a	n/a
34	CTCF	chr8:4644640-4644790	HEK293	kidney:	n/a	n/a
35	CTCF	chr8:4644700-4644850	GM12869	blood:	n/a	n/a
36	CTCF	chr8:4644647-4644651	HepG2	liver:	n/a	n/a
37	CTCF	chr8:4644625-4644807	SK-N-SH_RA	brain:	n/a	n/a
38	CTCF	chr8:4612266-4612290	GM13976	blood:	n/a	n/a
39	CTCF	chr8:4644618-4644836	HepG2	liver:	n/a	n/a
40	CTCF	chr8:4644640-4644790	GM12872	blood:	n/a	n/a
41	CTCF	chr8:4644642-4644821	K562	blood:	n/a	n/a
42	CTCF	chr8:4644611-4644850	H1-hESC	embryonic stem cell:	n/a	n/a
43	CTCF	chr8:4644516-4644932	H1-hESC	embryonic stem cell:	n/a	n/a
44	CTCF	chr8:4644620-4644770	WERI-Rb-1	eye:	n/a	n/a
45	CTCF	chr8:4644652-4644813	HepG2	liver:	n/a	n/a
46	CTCF	chr8:4644647-4644806	GM12891	blood:	n/a	n/a
47	CTCF	chr8:4644640-4644790	A549	lung:	n/a	n/a
48	CTCF	chr8:4644587-4644847	H1-hESC	embryonic stem cell:	n/a	n/a
49	CTCF	chr8:4644597-4644867	HepG2	liver:	n/a	n/a
50	CTCF	chr8:4644680-4644748	Pancreas_OC	pancreas:	n/a	n/a

(count:610 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:4629524-4629574	HL-60	blood:	n/a
2	chr8:4601508-4601558	GM12891	blood:	n/a
3	chr8:4583355-4583405	HAEpiC	amniotic membrane:	n/a
4	chr8:4637584-4637634	RPTEC	kidney:	n/a
5	chr8:4629524-4629574	U87	brain:	n/a
6	chr8:4644719-4644769	HAEpiC	amniotic membrane:	n/a
7	chr8:4573688-4573738	HCM	heart:	n/a
8	chr8:4583386-4583436	SK-N-SH	brain:	n/a
9	chr8:4637584-4637634	AG04450	lung:	fetal
10	chr8:4617087-4617137	IMR90	lung:	fetal
11	chr8:4637584-4637634	HPAEpiC	pulmonary alveolar:	n/a
12	chr8:4637584-4637634	GM12891	blood:	n/a
13	chr8:4644739-4644789	MCF10A-Er-Src	breast:	n/a
14	chr8:4573688-4573738	SKMC	muscle:	n/a
15	chr8:4573688-4573738	ProgFib	skin:	n/a
16	chr8:4583386-4583436	PrEC	prostate:	n/a
17	chr8:4601579-4601629	K562	blood:	n/a
18	chr8:4601579-4601629	MCF-7	breast:	n/a
19	chr8:4617087-4617137	HepG2	liver:	n/a
20	chr8:4617087-4617137	NHBE	bronchial:	n/a
21	chr8:4644739-4644789	T-47D	breast:	n/a
22	chr8:4583386-4583436	NH-A	brain:	n/a
23	chr8:4644739-4644789	HCM	heart:	n/a
24	chr8:4573688-4573738	HepG2	liver:	n/a
25	chr8:4644739-4644789	Caco-2	colon:	n/a
26	chr8:4644719-4644769	HUVEC	blood vessel:	n/a
27	chr8:4637584-4637634	HIPEpiC	eye:	n/a
28	chr8:4601579-4601629	AG09309	skin:	n/a
29	chr8:4573688-4573738	AG04450	lung:	fetal
30	chr8:4601579-4601629	NHBE	bronchial:	n/a
31	chr8:4583355-4583405	HPAEpiC	pulmonary alveolar:	n/a
32	chr8:4637584-4637634	K562	blood:	n/a
33	chr8:4644739-4644789	CMK	blood:	n/a
34	chr8:4644719-4644769	HCF	heart:	n/a
35	chr8:4644739-4644789	ovcar-3	ovarian:	n/a
36	chr8:4629524-4629574	SK-N-SH_RA	brain:	n/a
37	chr8:4637584-4637634	SK-N-MC	brain:	n/a
38	chr8:4601508-4601558	AG09309	skin:	n/a
39	chr8:4629524-4629574	Jurkat	blood:	n/a
40	chr8:4644719-4644769	BE2_C	brain:	n/a
41	chr8:4583386-4583436	ECC-1	luminal epithelium:	n/a
42	chr8:4601579-4601629	Hela-S3	cervix:	n/a
43	chr8:4601508-4601558	NHBE	bronchial:	n/a
44	chr8:4583386-4583436	RPTEC	kidney:	n/a
45	chr8:4644719-4644769	HRE	kidney:	n/a
46	chr8:4583386-4583436	AG04450	lung:	fetal
47	chr8:4583355-4583405	IMR90	lung:	fetal
48	chr8:4583386-4583436	HCT-116	colon:	n/a
49	chr8:4583386-4583436	NHBE	bronchial:	n/a
50	chr8:4629524-4629574	GM12891	blood:	n/a

(count:4 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:4614268..4616817-chr8:4617498..4620007,2	K562	blood:
2	chr8:4614268..4616817-chr8:4617498..4620007,2	K562	blood:
3	chr21:30519178..30519958-chr8:4582339..4582839,2	MCF-7	breast:
4	chr2:220553002..220553652-chr8:4562250..4563228,2	HCT-116	colon:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MCPH1-7	chr8:4644854-4646106	NONHSAT124751

No data

Variant related genes	Relation type
PAICSP4	TF binding region
PAICSP4	CpG island

Extended variants
information (count: 7187 )
Associated
traits (count: 126 )

Variant overlapped rSNPs/rCNVs (count:7187 , 50 per page) page: 1 2 3 4 5 6 7 ... 144

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs545893844	chr8:4558400-4558401	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs574476155	chr8:4558403-4558404	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs558028243	chr8:4558455-4558456	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs576592036	chr8:4558456-4558457	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs369822988	chr8:4558476-4558477	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs373339486	chr8:4558484-4558485	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs543736356	chr8:4558490-4558491	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs189351272	chr8:4558493-4558494	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs562440106	chr8:4558532-4558533	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs115951092	chr8:4558539-4558540	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs386721363	chr8:4558550-4558551	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs559395340	chr8:4558551-4558552	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs76008349	chr8:4558565-4558566	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs138078406	chr8:4558566-4558567	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs569721400	chr8:4558583-4558584	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs181649361	chr8:4558587-4558588	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs149547077	chr8:4558588-4558589	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs185934983	chr8:4558613-4558614	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs535453749	chr8:4558615-4558616	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs188690814	chr8:4558619-4558620	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs181339344	chr8:4558634-4558635	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs186119151	chr8:4558638-4558639	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs539511918	chr8:4558650-4558651	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs374951114	chr8:4558656-4558657	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs369364185	chr8:4558676-4558677	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs114415718	chr8:4558678-4558679	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs372494432	chr8:4558684-4558685	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs147219750	chr8:4558688-4558689	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs190972806	chr8:4558692-4558693	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs377063502	chr8:4558693-4558694	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs541757939	chr8:4558702-4558703	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs369830034	chr8:4558709-4558710	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs577737713	chr8:4558722-4558723	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs184015768	chr8:4558730-4558731	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs563429054	chr8:4558737-4558738	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs373986860	chr8:4558744-4558745	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs73512943	chr8:4558746-4558747	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs549204926	chr8:4558765-4558766	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs560750514	chr8:4558780-4558781	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs527718099	chr8:4558805-4558806	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs115199740	chr8:4558810-4558811	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs541787891	chr8:4558813-4558814	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs528768462	chr8:4558827-4558828	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs5889050	chr8:4558839-4558840	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs200233918	chr8:4558845-4558846	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs397780014	chr8:4558852-4558853	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs80123278	chr8:4558854-4558855	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs77774947	chr8:4558855-4558856	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs190767237	chr8:4558871-4558872	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs114858280	chr8:4558896-4558897	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:126)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	16573809	CNVD
Myelofibrosis	22110671	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
abnormal development	18461090	CNVD
Crohn''s disease	19220326	CNVD
Psoriasis	19220326	CNVD
Prostate cancer	21965145	CNVD
Prostate cancer	18515986	CNVD
Chronic obstructive pulmonary disease	20378733	CNVD
Autism	18414403	CNVD
Cancer	21183584	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Breast cancer	17603634	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Ovarian cancer	20844748	CNVD
Cervical cancer	17311676	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Schizophrenia	20877625	CNVD
Disorders of sex development	21048976	CNVD
Colorectal cancer	16272173	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Breast cancer	17001317	CNVD
Thyroid cancer	19087340	CNVD
Multiple myeloma	16616336	CNVD
Hepatocellular carcinoma	22174799	CNVD
Heart disease	21282601	CNVD
T-cell lymphomas	19863542	CNVD
Ovarian cancer	22174824	CNVD
Colorectal cancer	21297112	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	17133270	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Breast cancer	17393978	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Breast cancer	20837533	CNVD
Squamous cell cancer	21044232	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	22429812	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Basal cell lymphoma	21115979	CNVD
Breast cancer	21264507	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Oral cancer	21386901	CNVD
Prostate cancer	21088497	CNVD
Breast cancer	20940404	CNVD
Colorectal cancer	19359472	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Gastric cancer	17167181	CNVD
Prostate cancer	16705090	CNVD
8p-syndrome	17576883	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Prostate cancer	17245344	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Cancer	16751803	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Breast cancer	21785460	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute myeloid leukemia	20729466	CNVD
Ductal carcinoma	22052326	CNVD
Breast cancer	21509527	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Epilepsy	22083797	CNVD
Acute myeloid leukemia	21251322	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
Congenital diaphragmatic hernia	21064195	CNVD
Breast cancer	21364760	CNVD
Cancer	20164920	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Non-small cell lung cancer	21829676	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Prostate cancer	17217626	CNVD
Developmental delay	19128483	CNVD
Neuroticism	17667963	CNVD
Leukoplakia	24403051	CNVD
Intellectual disability	22045946	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16608533	CNVD
Seminomas	18059402	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Colorectal cancer	16774939	CNVD
Colorectal cancer	21645411	CNVD
Colorectal cancer	22014273	CNVD
Lung squamous cell carcinoma	22363434	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Chronic myeloid leukemia	21384125	CNVD
Tetralogy of Fallot	22912587	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD

Chromatin state (count:129 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:4558400-4559000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
2	chr8:4562800-4563200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr8:4563200-4564200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr8:4564200-4565000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr8:4570600-4586800	Weak transcription	Cortex derived primary cultured neurospheres	brain
6	chr8:4573000-4573200	Enhancers	HUES48 Cell Line	embryonic stem cell
7	chr8:4573000-4573600	Enhancers	Fetal Heart	heart
8	chr8:4573200-4573600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr8:4573200-4573600	Enhancers	H9 Cell Line	embryonic stem cell
10	chr8:4573200-4573600	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
11	chr8:4573200-4574000	Enhancers	ES-I3 Cell Line	embryonic stem cell
12	chr8:4573200-4574000	Enhancers	H1 Cell Line	embryonic stem cell
13	chr8:4573200-4574000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr8:4573200-4574000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr8:4573200-4574200	Enhancers	iPS-20b Cell Line	embryonic stem cell
16	chr8:4573400-4573800	Enhancers	Brain Cingulate Gyrus	brain
17	chr8:4573400-4574000	Enhancers	HUES6 Cell Line	embryonic stem cell
18	chr8:4573400-4574000	Enhancers	iPS-15b Cell Line	embryonic stem cell
19	chr8:4573400-4574000	Enhancers	Brain Substantia Nigra	brain
20	chr8:4573400-4574000	Enhancers	Fetal Lung	lung
21	chr8:4573400-4574200	Enhancers	Brain Hippocampus Middle	brain
22	chr8:4573600-4573800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr8:4573600-4574000	Enhancers	HUES48 Cell Line	embryonic stem cell
24	chr8:4573600-4574200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
25	chr8:4573600-4574200	Enhancers	Brain Inferior Temporal Lobe	brain
26	chr8:4586800-4587800	Enhancers	Cortex derived primary cultured neurospheres	brain
27	chr8:4587800-4592600	Weak transcription	Cortex derived primary cultured neurospheres	brain
28	chr8:4592400-4592800	Enhancers	ES-I3 Cell Line	embryonic stem cell
29	chr8:4592400-4593200	Enhancers	Colon Smooth Muscle	Colon
30	chr8:4592600-4593200	Enhancers	Cortex derived primary cultured neurospheres	brain
31	chr8:4593200-4593600	Weak transcription	Cortex derived primary cultured neurospheres	brain
32	chr8:4593600-4593800	Enhancers	Cortex derived primary cultured neurospheres	brain
33	chr8:4593800-4616600	Weak transcription	Cortex derived primary cultured neurospheres	brain
34	chr8:4597200-4597600	Enhancers	Brain Inferior Temporal Lobe	brain
35	chr8:4597200-4598000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
36	chr8:4610600-4612600	Enhancers	Fetal Brain Male	brain
37	chr8:4611000-4611400	Enhancers	Stomach Smooth Muscle	stomach
38	chr8:4615000-4616800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
39	chr8:4616600-4617400	Strong transcription	Cortex derived primary cultured neurospheres	brain
40	chr8:4616800-4617000	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
41	chr8:4617000-4617200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
42	chr8:4617200-4617800	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
43	chr8:4617400-4619600	Weak transcription	Cortex derived primary cultured neurospheres	brain
44	chr8:4617800-4619600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
45	chr8:4619600-4620200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
46	chr8:4619600-4620600	Enhancers	Brain Angular Gyrus	brain
47	chr8:4619600-4621000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
48	chr8:4619600-4623200	Enhancers	Cortex derived primary cultured neurospheres	brain
49	chr8:4619800-4620400	Enhancers	Brain Hippocampus Middle	brain
50	chr8:4619800-4621000	Enhancers	Brain Substantia Nigra	brain

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