Variant report

Variant	esv34237
Chromosome Location	chr8:4617778-4709513
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	chr8:4691580-4691808	HepG2	liver:	n/a	n/a
2	BACH1	chr8:4703337-4703643	H1-hESC	embryonic stem cell:	n/a	n/a
3	BHLHE40	chr8:4691724-4691748	GM12878	blood:	n/a	n/a
4	CEBPB	chr8:4668991-4669179	HepG2	liver:	n/a	chr8:4669056-4669067
5	CHD2	chr8:4644622-4644850	H1-hESC	embryonic stem cell:	n/a	n/a
6	CHD2	chr8:4654890-4654920	HepG2	liver:	n/a	n/a
7	CTCF	chr8:4695440-4695590	AG10803	skin:	n/a	chr8:4695499-4695512 chr8:4695496-4695514 chr8:4695498-4695519 chr8:4695499-4695508
8	CTCF	chr8:4695440-4695590	GM12872	blood:	n/a	chr8:4695499-4695512 chr8:4695496-4695514 chr8:4695498-4695519 chr8:4695499-4695508
9	CTCF	chr8:4644600-4644750	SAEC	small airway:	n/a	n/a
10	CTCF	chr8:4691183-4691965	SK-N-SH	brain:	n/a	chr8:4691557-4691578 chr8:4691555-4691573
11	CTCF	chr8:4691351-4691757	GM12878	blood:	n/a	chr8:4691557-4691578 chr8:4691555-4691573
12	CTCF	chr8:4695311-4695680	K562	blood:	n/a	chr8:4695499-4695512 chr8:4695496-4695514 chr8:4695498-4695519 chr8:4695499-4695508
13	CTCF	chr8:4691437-4691612	GM10266	blood:	n/a	chr8:4691557-4691578 chr8:4691555-4691573
14	CTCF	chr8:4644640-4644790	GM12865	blood:	n/a	n/a
15	CTCF	chr8:4691460-4691610	BE2_C	brain:	n/a	chr8:4691557-4691578 chr8:4691555-4691573
16	CTCF	chr8:4691500-4691650	Hela-S3	cervix:	n/a	chr8:4691557-4691578 chr8:4691555-4691573
17	CTCF	chr8:4691456-4691687	GM13977	blood:	n/a	chr8:4691557-4691578 chr8:4691555-4691573
18	CTCF	chr8:4695440-4695590	SK-N-SH_RA	brain:	n/a	chr8:4695499-4695512 chr8:4695496-4695514 chr8:4695498-4695519 chr8:4695499-4695508
19	CTCF	chr8:4695420-4695570	NB4	blood:	n/a	chr8:4695499-4695512 chr8:4695496-4695514 chr8:4695498-4695519 chr8:4695499-4695508
20	CTCF	chr8:4695410-4695617	K562	blood:	n/a	chr8:4695499-4695512 chr8:4695496-4695514 chr8:4695498-4695519 chr8:4695499-4695508
21	CTCF	chr8:4695406-4695628	MCF-7	breast:	n/a	chr8:4695499-4695512 chr8:4695496-4695514 chr8:4695498-4695519 chr8:4695499-4695508
22	CTCF	chr8:4695321-4695638	IMR90	lung:	n/a	chr8:4695499-4695512 chr8:4695496-4695514 chr8:4695498-4695519 chr8:4695499-4695508
23	CTCF	chr8:4691540-4691690	GM12878	blood:	n/a	chr8:4691557-4691578 chr8:4691555-4691573
24	CTCF	chr8:4690760-4690910	GM12873	blood:	n/a	n/a
25	CTCF	chr8:4695480-4695630	GM06990	blood:	n/a	chr8:4695499-4695512 chr8:4695496-4695514 chr8:4695498-4695519 chr8:4695499-4695508
26	CTCF	chr8:4695393-4695617	Spleen_OC	spleen:	n/a	chr8:4695499-4695512 chr8:4695496-4695514 chr8:4695498-4695519 chr8:4695499-4695508
27	CTCF	chr8:4695440-4695590	GM12875	blood:	n/a	chr8:4695499-4695512 chr8:4695496-4695514 chr8:4695498-4695519 chr8:4695499-4695508
28	CTCF	chr8:4644587-4644847	H1-hESC	embryonic stem cell:	n/a	n/a
29	CTCF	chr8:4691480-4691630	HRPEpiC	eye:	n/a	chr8:4691557-4691578 chr8:4691555-4691573
30	CTCF	chr8:4691471-4691652	Pancreas_OC	pancreas:	n/a	chr8:4691557-4691578 chr8:4691555-4691573
31	CTCF	chr8:4695399-4695642	GM12891	blood:	n/a	chr8:4695499-4695512 chr8:4695496-4695514 chr8:4695498-4695519 chr8:4695499-4695508
32	CTCF	chr8:4695367-4695639	LNCaP	prostate:	n/a	chr8:4695499-4695512 chr8:4695496-4695514 chr8:4695498-4695519 chr8:4695499-4695508
33	CTCF	chr8:4691462-4691663	LNCaP	prostate:	n/a	chr8:4691557-4691578 chr8:4691555-4691573
34	CTCF	chr8:4691469-4691652	A549	lung:	n/a	chr8:4691557-4691578 chr8:4691555-4691573
35	CTCF	chr8:4695420-4695570	HCPEpiC	choroid plexus:	n/a	chr8:4695499-4695512 chr8:4695496-4695514 chr8:4695498-4695519 chr8:4695499-4695508
36	CTCF	chr8:4691469-4691568	GM19240	blood:	n/a	n/a
37	CTCF	chr8:4695420-4695570	HEEpiC	esophagus:	n/a	chr8:4695499-4695512 chr8:4695496-4695514 chr8:4695498-4695519 chr8:4695499-4695508
38	CTCF	chr8:4644600-4644750	GM12871	blood:	n/a	n/a
39	CTCF	chr8:4632207-4632286	Lung_OC	lung:	n/a	n/a
40	CTCF	chr8:4691460-4691610	AG09309	skin:	n/a	chr8:4691557-4691578 chr8:4691555-4691573
41	CTCF	chr8:4644640-4644790	GM12872	blood:	n/a	n/a
42	CTCF	chr8:4691480-4691630	HRE	kidney:	n/a	chr8:4691557-4691578 chr8:4691555-4691573
43	CTCF	chr8:4695440-4695590	AG09319	gingival:	n/a	chr8:4695499-4695512 chr8:4695496-4695514 chr8:4695498-4695519 chr8:4695499-4695508
44	CTCF	chr8:4691380-4691530	A549	lung:	n/a	n/a
45	CTCF	chr8:4695460-4695610	GM12874	blood:	n/a	chr8:4695499-4695512 chr8:4695496-4695514 chr8:4695498-4695519 chr8:4695499-4695508
46	CTCF	chr8:4691491-4691512	A549	lung:	n/a	n/a
47	CTCF	chr8:4695414-4695626	H1-hESC	embryonic stem cell:	n/a	chr8:4695499-4695512 chr8:4695496-4695514 chr8:4695498-4695519 chr8:4695499-4695508
48	CTCF	chr8:4695400-4695550	GM12872	blood:	n/a	chr8:4695499-4695512 chr8:4695496-4695514 chr8:4695498-4695519 chr8:4695499-4695508
49	CTCF	chr8:4691384-4691641	SK-N-SH_RA	brain:	n/a	chr8:4691557-4691578 chr8:4691555-4691573
50	CTCF	chr8:4691520-4691670	BJ	skin:	n/a	chr8:4691557-4691578 chr8:4691555-4691573

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:4644719-4644769	GM12878	blood:	n/a
2	chr8:4644719-4644769	HepG2	liver:	n/a
3	chr8:4644719-4644769	HCF	heart:	n/a
4	chr8:4629524-4629574	LNCaP	prostate:	n/a
5	chr8:4644739-4644789	BE2_C	brain:	n/a
6	chr8:4644719-4644769	Hela-S3	cervix:	n/a
7	chr8:4637584-4637634	AG04450	lung:	fetal
8	chr8:4637584-4637634	GM12878	blood:	n/a
9	chr8:4637584-4637634	SK-N-SH_RA	brain:	n/a
10	chr8:4644739-4644789	GM19239	blood:	n/a
11	chr8:4637584-4637634	PFSK-1	brain:	n/a
12	chr8:4644739-4644789	NT2-D1	testis:	n/a
13	chr8:4644739-4644789	HRE	kidney:	n/a
14	chr8:4629524-4629574	SK-N-SH	brain:	n/a
15	chr8:4644719-4644769	AG10803	skin:	n/a
16	chr8:4629524-4629574	K562	blood:	n/a
17	chr8:4637584-4637634	PANC-1	pancreas:	n/a
18	chr8:4644739-4644789	GM12892	blood:	n/a
19	chr8:4644719-4644769	HRE	kidney:	n/a
20	chr8:4644739-4644789	GM12891	blood:	n/a
21	chr8:4644719-4644769	AG09319	gingival:	n/a
22	chr8:4644719-4644769	Hepatocyte	liver:	n/a
23	chr8:4644719-4644769	GM19239	blood:	n/a
24	chr8:4644739-4644789	T-47D	breast:	n/a
25	chr8:4629524-4629574	MCF-7	breast:	n/a
26	chr8:4637584-4637634	HPAEpiC	pulmonary alveolar:	n/a
27	chr8:4644719-4644769	U87	brain:	n/a
28	chr8:4629524-4629574	HCF	heart:	n/a
29	chr8:4644739-4644789	HCPEpiC	choroid plexus:	n/a
30	chr8:4629524-4629574	NHDF-neo	bronchial:	n/a
31	chr8:4637584-4637634	ovcar-3	ovarian:	n/a
32	chr8:4644739-4644789	HepG2	liver:	n/a
33	chr8:4644719-4644769	T-47D	breast:	n/a
34	chr8:4629524-4629574	T-47D	breast:	n/a
35	chr8:4644739-4644789	ECC-1	luminal epithelium:	n/a
36	chr8:4644719-4644769	HIPEpiC	eye:	n/a
37	chr8:4637584-4637634	NH-A	brain:	n/a
38	chr8:4644719-4644769	NB4	blood:	n/a
39	chr8:4629524-4629574	NH-A	brain:	n/a
40	chr8:4644739-4644789	HCF	heart:	n/a
41	chr8:4644739-4644789	HPAEpiC	pulmonary alveolar:	n/a
42	chr8:4644739-4644789	AoSMC	blood vessel:	n/a
43	chr8:4644739-4644789	ovcar-3	ovarian:	n/a
44	chr8:4644739-4644789	Jurkat	blood:	n/a
45	chr8:4644719-4644769	Caco-2	colon:	n/a
46	chr8:4629524-4629574	HCT-116	colon:	n/a
47	chr8:4644719-4644769	H1-hESC	embryonic stem cell:	embryo
48	chr8:4644739-4644789	AG04450	lung:	fetal
49	chr8:4644739-4644789	HRPEpiC	eye:	n/a
50	chr8:4644719-4644769	NT2-D1	testis:	n/a

No.	Distal block	Cell Line	Cell type
1	chr8:4695059..4696118-chr8:4854167..4855161,8	MCF-7	breast:
2	chr8:4614268..4616817-chr8:4617498..4620007,2	K562	blood:
3	chr8:4695207..4695958-chr8:4732618..4733342,2	MCF-7	breast:
4	chr8:4696947..4699899-chr8:4702177..4705050,3	K562	blood:
5	chr8:4696947..4699899-chr8:4702177..4705050,3	K562	blood:

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

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

Extended variants
information (count: 4818 )
Associated
traits (count: 125 )

Variant overlapped rSNPs/rCNVs (count:4818 , 50 per page) page: 1 2 3 4 5 6 7 ... 97

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1350307	chr8:4617778-4617779	Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs1379326	chr8:4617810-4617811	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance disease
3	rs186415173	chr8:4617811-4617812	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs554434770	chr8:4617825-4617826	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs572978428	chr8:4617827-4617828	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs553232824	chr8:4617828-4617829	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs140262744	chr8:4617850-4617851	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs73661116	chr8:4617881-4617882	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs533405375	chr8:4617883-4617884	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs548729972	chr8:4617923-4617924	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs190803877	chr8:4617932-4617933	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs377073262	chr8:4617935-4617936	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs530878595	chr8:4617943-4617944	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs549443923	chr8:4617952-4617953	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs376138573	chr8:4617954-4617955	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs182636524	chr8:4618006-4618007	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs188043348	chr8:4618034-4618035	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs546933269	chr8:4618042-4618043	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs571568387	chr8:4618073-4618074	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs538251047	chr8:4618089-4618090	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs145354755	chr8:4618090-4618091	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs557928376	chr8:4618104-4618105	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs28377110	chr8:4618112-4618113	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs535996271	chr8:4618124-4618125	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs116966145	chr8:4618125-4618126	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs573000208	chr8:4618129-4618130	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs79150251	chr8:4618156-4618157	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs558898058	chr8:4618161-4618162	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs548946355	chr8:4618167-4618168	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs577159599	chr8:4618183-4618184	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs6981893	chr8:4618190-4618191	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs2607553	chr8:4618197-4618198	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs530914259	chr8:4618217-4618218	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs542802200	chr8:4618227-4618228	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs73177520	chr8:4618256-4618257	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs528690273	chr8:4618258-4618259	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs546742617	chr8:4618283-4618284	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs574669184	chr8:4618320-4618321	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs571630391	chr8:4618322-4618323	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs532633725	chr8:4618324-4618325	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs550847377	chr8:4618332-4618333	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs568787770	chr8:4618345-4618346	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs140676418	chr8:4618366-4618367	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs192504977	chr8:4618368-4618369	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs183123553	chr8:4618375-4618376	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs143806956	chr8:4618378-4618379	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs1673243	chr8:4618380-4618381	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs558754770	chr8:4618399-4618400	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs77575729	chr8:4618409-4618410	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs538174436	chr8:4618412-4618413	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:125)

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

Chromatin state (count:117 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:4617200-4617800	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
2	chr8:4617400-4619600	Weak transcription	Cortex derived primary cultured neurospheres	brain
3	chr8:4617800-4619600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
4	chr8:4619600-4620200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
5	chr8:4619600-4620600	Enhancers	Brain Angular Gyrus	brain
6	chr8:4619600-4621000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr8:4619600-4623200	Enhancers	Cortex derived primary cultured neurospheres	brain
8	chr8:4619800-4620400	Enhancers	Brain Hippocampus Middle	brain
9	chr8:4619800-4621000	Enhancers	Brain Substantia Nigra	brain
10	chr8:4620000-4620400	Enhancers	H1 Cell Line	embryonic stem cell
11	chr8:4620000-4620400	Enhancers	iPS-20b Cell Line	embryonic stem cell
12	chr8:4620000-4620400	Active TSS	Brain Inferior Temporal Lobe	brain
13	chr8:4620000-4621000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr8:4620200-4620600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr8:4620200-4620600	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
16	chr8:4620200-4620600	Active TSS	Brain Anterior Caudate	brain
17	chr8:4620200-4620800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr8:4620400-4620800	Flanking Active TSS	Brain Hippocampus Middle	brain
19	chr8:4620400-4621000	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
20	chr8:4620400-4621800	Enhancers	Brain Cingulate Gyrus	brain
21	chr8:4620600-4621000	Enhancers	Brain Anterior Caudate	brain
22	chr8:4620600-4621800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
23	chr8:4620600-4624000	Weak transcription	Brain Angular Gyrus	brain
24	chr8:4620800-4621000	Enhancers	Brain Hippocampus Middle	brain
25	chr8:4620800-4622200	Enhancers	Brain Germinal Matrix	brain
26	chr8:4621000-4630800	Weak transcription	Brain Inferior Temporal Lobe	brain
27	chr8:4621800-4625000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
28	chr8:4623200-4625000	Weak transcription	Cortex derived primary cultured neurospheres	brain
29	chr8:4624800-4625200	ZNF genes & repeats	Brain Angular Gyrus	brain
30	chr8:4625000-4625200	ZNF genes & repeats	Brain Cingulate Gyrus	brain
31	chr8:4625000-4625400	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
32	chr8:4625200-4630600	Weak transcription	Brain Cingulate Gyrus	brain
33	chr8:4625200-4631400	Weak transcription	Brain Angular Gyrus	brain
34	chr8:4628200-4629800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
35	chr8:4629800-4630800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr8:4630200-4630800	Enhancers	Brain Hippocampus Middle	brain
37	chr8:4630600-4630800	Enhancers	Brain Cingulate Gyrus	brain
38	chr8:4630800-4631200	Enhancers	Cortex derived primary cultured neurospheres	brain
39	chr8:4630800-4631200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
40	chr8:4630800-4631200	Active TSS	Brain Anterior Caudate	brain
41	chr8:4630800-4631200	Active TSS	Brain Hippocampus Middle	brain
42	chr8:4630800-4631200	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
43	chr8:4630800-4637000	Weak transcription	Brain Cingulate Gyrus	brain
44	chr8:4631200-4631600	Enhancers	Brain Inferior Temporal Lobe	brain
45	chr8:4631200-4632400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr8:4631400-4631600	Enhancers	Brain Angular Gyrus	brain
47	chr8:4631600-4638800	Weak transcription	Brain Angular Gyrus	brain
48	chr8:4632200-4632600	Enhancers	HUES48 Cell Line	embryonic stem cell
49	chr8:4635800-4636800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
50	chr8:4636000-4636200	Enhancers	Fetal Kidney	kidney

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