Variant report

Variant	nsv831341
Chromosome Location	chr8:63658694-63852213
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	BACH1	chr8:63699427-63699449	H1-hESC	embryonic stem cell:	n/a	n/a
2	BATF	chr8:63837251-63837534	GM12878	blood:	n/a	n/a
3	BATF	chr8:63833245-63833447	GM12878	blood:	n/a	chr8:63833338-63833349
4	BATF	chr8:63771581-63771822	GM12878	blood:	n/a	n/a
5	BATF	chr8:63771525-63771873	GM12878	blood:	n/a	n/a
6	BATF	chr8:63768987-63769287	GM12878	blood:	n/a	chr8:63769159-63769170 chr8:63769160-63769170
7	BATF	chr8:63837211-63837498	GM12878	blood:	n/a	n/a
8	BATF	chr8:63833259-63833459	GM12878	blood:	n/a	chr8:63833338-63833349
9	BCL11A	chr8:63800466-63800690	GM12878	blood:	n/a	n/a
10	BCL3	chr8:63660856-63661129	GM12878	blood:	n/a	n/a
11	BCL3	chr8:63660810-63661178	GM12878	blood:	n/a	n/a
12	BHLHE40	chr8:63800468-63801027	GM12878	blood:	n/a	n/a
13	BHLHE40	chr8:63818482-63818843	GM12878	blood:	n/a	n/a
14	BHLHE40	chr8:63819107-63819312	GM12878	blood:	n/a	n/a
15	BHLHE40	chr8:63709354-63709419	GM12878	blood:	n/a	n/a
16	BRCA1	chr8:63814485-63814782	H1-hESC	embryonic stem cell:	n/a	n/a
17	BRCA1	chr8:63814731-63814733	GM12878	blood:	n/a	n/a
18	CBX3	chr8:63721317-63721624	K562	blood:	n/a	n/a
19	CBX3	chr8:63721432-63721611	K562	blood:	n/a	n/a
20	CEBPB	chr8:63819828-63820100	HepG2	liver:	n/a	chr8:63819936-63819947
21	CEBPB	chr8:63813708-63813896	HepG2	liver:	n/a	n/a
22	CEBPB	chr8:63667291-63667532	HepG2	liver:	n/a	chr8:63667401-63667410 chr8:63667401-63667410 chr8:63667401-63667410 chr8:63667401-63667410 chr8:63667401-63667412 chr8:63667399-63667412 chr8:63667399-63667412 chr8:63667399-63667410
23	CEBPB	chr8:63819847-63819956	H1-hESC	embryonic stem cell:	n/a	chr8:63819936-63819947
24	CEBPB	chr8:63838584-63839051	HepG2	liver:	n/a	chr8:63838760-63838771 chr8:63838759-63838770
25	CEBPB	chr8:63838587-63838926	IMR90	lung:	n/a	chr8:63838760-63838771 chr8:63838759-63838770
26	CEBPB	chr8:63838636-63838928	K562	blood:	n/a	chr8:63838760-63838771 chr8:63838759-63838770
27	CEBPB	chr8:63838594-63838891	A549	lung:	n/a	chr8:63838760-63838771 chr8:63838759-63838770
28	CEBPB	chr8:63659290-63659551	HepG2	liver:	n/a	n/a
29	CEBPB	chr8:63837446-63837533	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPB	chr8:63780063-63780234	HepG2	liver:	n/a	n/a
31	CEBPB	chr8:63838698-63839121	H1-hESC	embryonic stem cell:	n/a	chr8:63838760-63838771 chr8:63838759-63838770
32	CEBPB	chr8:63667258-63667565	IMR90	lung:	n/a	chr8:63667401-63667410 chr8:63667401-63667410 chr8:63667401-63667410 chr8:63667401-63667410 chr8:63667401-63667412 chr8:63667399-63667412 chr8:63667399-63667412 chr8:63667399-63667410
33	CEBPB	chr8:63819853-63820103	A549	lung:	n/a	chr8:63819936-63819947
34	CHD1	chr8:63800431-63800581	GM12878	blood:	n/a	n/a
35	CHD2	chr8:63818521-63818768	GM12878	blood:	n/a	n/a
36	CHD2	chr8:63800514-63800926	GM12878	blood:	n/a	n/a
37	CHD2	chr8:63814429-63814777	H1-hESC	embryonic stem cell:	n/a	n/a
38	CTCF	chr8:63776683-63776807	GM19240	blood:	n/a	n/a
39	CTCF	chr8:63814481-63814781	GM12891	blood:	n/a	chr8:63814640-63814658 chr8:63814581-63814594
40	CTCF	chr8:63814477-63814777	GM12892	blood:	n/a	chr8:63814640-63814658 chr8:63814581-63814594
41	CTCF	chr8:63678900-63679050	HBMEC	blood vessel:	n/a	n/a
42	CTCF	chr8:63814560-63814710	SK-N-SH_RA	brain:	n/a	chr8:63814640-63814658 chr8:63814581-63814594
43	CTCF	chr8:63814580-63814730	RPTEC	kidney:	n/a	chr8:63814640-63814658 chr8:63814581-63814594
44	CTCF	chr8:63814580-63814730	GM12878	blood:	n/a	chr8:63814581-63814594 chr8:63814640-63814658
45	CTCF	chr8:63776660-63776810	GM12871	blood:	n/a	n/a
46	CTCF	chr8:63814480-63814630	BE2_C	brain:	n/a	chr8:63814581-63814594
47	CTCF	chr8:63776680-63776830	SK-N-SH_RA	brain:	n/a	n/a
48	CTCF	chr8:63678893-63679064	GM10266	blood:	n/a	n/a
49	CTCF	chr8:63814494-63814770	MCF-7	breast:	n/a	chr8:63814640-63814658 chr8:63814581-63814594
50	CTCF	chr8:63817133-63817152	ProgFib	skin:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:63776508-63776558	HAEpiC	amniotic membrane:	n/a
2	chr8:63776508-63776558	HAEpiC	amniotic membrane:	n/a
3	chr8:63662874-63662924	PrEC	prostate:	n/a
4	chr8:63662874-63662924	NT2-D1	testis:	n/a
5	chr8:63777430-63777480	A549	lung:	n/a
6	chr8:63776508-63776558	GM12891	blood:	n/a
7	chr8:63776642-63776692	BE2_C	brain:	n/a
8	chr8:63776755-63776805	HL-60	blood:	n/a
9	chr8:63662874-63662924	U87	brain:	n/a
10	chr8:63776755-63776805	NHBE	bronchial:	n/a
11	chr8:63776762-63776812	AG04450	lung:	fetal
12	chr8:63776762-63776812	BE2_C	brain:	n/a
13	chr8:63776755-63776805	HRE	kidney:	n/a
14	chr8:63776642-63776692	NHDF-neo	bronchial:	n/a
15	chr8:63776508-63776558	HepG2	liver:	n/a
16	chr8:63776762-63776812	H1-hESC	embryonic stem cell:	embryo
17	chr8:63776508-63776558	ProgFib	skin:	n/a
18	chr8:63662874-63662924	HepG2	liver:	n/a
19	chr8:63777430-63777480	HUVEC	blood vessel:	n/a
20	chr8:63776755-63776805	U87	brain:	n/a
21	chr8:63776642-63776692	T-47D	breast:	n/a
22	chr8:63776762-63776812	HRCEpiC	kidney:	n/a
23	chr8:63777430-63777480	ovcar-3	ovarian:	n/a
24	chr8:63776508-63776558	SK-N-MC	brain:	n/a
25	chr8:63776508-63776558	HL-60	blood:	n/a
26	chr8:63776508-63776558	AG04449	skin:	fetal
27	chr8:63776755-63776805	ProgFib	skin:	n/a
28	chr8:63776642-63776692	SAEC	small airway:	n/a
29	chr8:63776642-63776692	HNPCEpiC	eye:	n/a
30	chr8:63776755-63776805	HUVEC	blood vessel:	n/a
31	chr8:63777430-63777480	BJ	skin:	n/a
32	chr8:63776508-63776558	ovcar-3	ovarian:	n/a
33	chr8:63776642-63776692	LNCaP	prostate:	n/a
34	chr8:63776755-63776805	Caco-2	colon:	n/a
35	chr8:63777430-63777480	HepG2	liver:	n/a
36	chr8:63776642-63776692	HL-60	blood:	n/a
37	chr8:63776762-63776812	T-47D	breast:	n/a
38	chr8:63662874-63662924	GM06990	blood:	n/a
39	chr8:63776755-63776805	NB4	blood:	n/a
40	chr8:63776508-63776558	NT2-D1	testis:	n/a
41	chr8:63776755-63776805	HMEC	breast:	n/a
42	chr8:63776755-63776805	CMK	blood:	n/a
43	chr8:63776508-63776558	ECC-1	luminal epithelium:	n/a
44	chr8:63777430-63777480	HMEC	breast:	n/a
45	chr8:63776762-63776812	SKMC	muscle:	n/a
46	chr8:63776755-63776805	SK-N-SH	brain:	n/a
47	chr8:63777430-63777480	NT2-D1	testis:	n/a
48	chr8:63776755-63776805	HAEpiC	amniotic membrane:	n/a
49	chr8:63776642-63776692	HAEpiC	amniotic membrane:	n/a
50	chr8:63776508-63776558	PFSK-1	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr8:63834445..63836856-chr8:63836928..63839834,2	K562	blood:
2	chr1:28832582..28833084-chr8:63789537..63790057,2	Hela-S3	cervix:
3	chr20:52479216..52480867-chr8:63834559..63837540,2	MCF-7	breast:
4	chr8:63677681..63680194-chr8:63684141..63687087,2	K562	blood:
5	chr8:63834445..63836856-chr8:63836928..63839834,2	K562	blood:
6	chr12:92008019..92008867-chr8:63749542..63750231,2	MCF-7	breast:
7	chr8:63677681..63680194-chr8:63684141..63687087,2	K562	blood:
8	chr8:63842222..63844345-chr8:63846508..63849240,2	K562	blood:
9	chr8:63842222..63844345-chr8:63846508..63849240,2	K562	blood:
10	chr10:1231043..1232833-chr8:63744046..63746893,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GGH-2	chr8:63775641-63776740	NONHSAT126908

Variant related genes	Relation type
ENSG00000253431	TF binding region
XRCC6P4	TF binding region
ENSG00000253431	CpG island
XRCC6P4	CpG island
ENSG00000185736	chromatin interactions
ENSG00000242125	chromatin interactions

Extended variants
information (count: 4330 )
Associated
traits (count: 98 )

Variant overlapped rSNPs/rCNVs (count:4330 , 50 per page) page: 1 2 3 4 5 6 7 ... 87

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs562152405	chr8:63658703-63658704	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs141340495	chr8:63658706-63658707	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs551106041	chr8:63658720-63658721	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs562960695	chr8:63658733-63658734	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs34166717	chr8:63658767-63658768	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs533641197	chr8:63658780-63658781	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs73683239	chr8:63658785-63658786	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs4739002	chr8:63658810-63658811	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs560049718	chr8:63658856-63658857	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs548609851	chr8:63658871-63658872	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs145123122	chr8:63658887-63658888	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs537549181	chr8:63658890-63658891	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs532157719	chr8:63658906-63658907	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs61145974	chr8:63658933-63658934	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs538861932	chr8:63658946-63658947	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs372789293	chr8:63658988-63658989	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs1480127	chr8:63659003-63659004	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
18	rs138862716	chr8:63659006-63659007	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs185902515	chr8:63659021-63659022	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs555801658	chr8:63659024-63659025	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs371991614	chr8:63659101-63659102	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs574050316	chr8:63659108-63659109	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs574929234	chr8:63659123-63659124	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs571774987	chr8:63659176-63659177	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs191108752	chr8:63659218-63659219	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs74388214	chr8:63659238-63659239	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs142053341	chr8:63659254-63659255	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs78548220	chr8:63659270-63659271	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs545244608	chr8:63659272-63659273	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs560404538	chr8:63659274-63659275	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs116233188	chr8:63659318-63659319	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs548525856	chr8:63659362-63659363	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs975688	chr8:63659367-63659368	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs143632173	chr8:63659409-63659410	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs549588014	chr8:63659422-63659423	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs570861331	chr8:63659439-63659440	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs75287413	chr8:63659445-63659446	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs374504803	chr8:63659457-63659458	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs79437525	chr8:63659462-63659463	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs148093471	chr8:63659496-63659497	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs201185620	chr8:63659497-63659498	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs368818581	chr8:63659516-63659517	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs183693168	chr8:63659523-63659524	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs565934055	chr8:63659524-63659525	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs371183258	chr8:63659527-63659528	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs374144864	chr8:63659528-63659529	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs368506597	chr8:63659555-63659556	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs371935351	chr8:63659569-63659570	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs536571888	chr8:63659594-63659595	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs141311198	chr8:63659601-63659602	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:98)

Disease	PMID	Source
Cancer	16751803	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Ewing''s sarcoma	21437220	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
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Seminomas	18059402	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Disorders of sex development	21048976	CNVD
Testicular cancer	18059402	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Cancer	20164919	CNVD
primary effusion lymphomas	17116491	CNVD
Esophageal cancer	20955586	CNVD
Multiple myeloma	16461302	CNVD
abnormal development	18461090	CNVD
Cancer	20164920	CNVD
Oral cancer	21386901	CNVD
Uveal melanoma	21693616	CNVD
Langer-Giedion syndrome	22283845	CNVD
Cancer	21637783	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	20632083	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	19627613	CNVD
Prostate cancer	21088497	CNVD
colon cancer	17210682	CNVD
Breast cancer	21264507	CNVD
Breast cancer	22028636	CNVD
Acute myeloid leukemia	16864856	CNVD
Salivary gland tumor	18059337	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Gastric cancer	17167181	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	16461572	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
head and neck squamous cell carcinoma	18028549	CNVD
Breast cancer	17001317	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	18628472	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Colorectal cancer	16272173	CNVD
Melanoma	22183965	CNVD
Cancer	21949371	CNVD
Non-small cell lung cancer	21829676	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Acute myeloid leukemia	21358987	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
small cell lung cancer	20016488	CNVD
Sezary syndrome	18413736	CNVD
Colorectal cancer	21645411	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Renal cell carcinoma	21215367	CNVD

Chromatin state (count:141 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:63649200-63660200	Weak transcription	Cortex derived primary cultured neurospheres	brain
2	chr8:63657600-63658800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
3	chr8:63658000-63659400	Weak transcription	Fetal Brain Female	brain
4	chr8:63658600-63662600	Weak transcription	Brain Germinal Matrix	brain
5	chr8:63659400-63660600	Strong transcription	Fetal Brain Female	brain
6	chr8:63660200-63661400	Strong transcription	Cortex derived primary cultured neurospheres	brain
7	chr8:63660600-63663400	Weak transcription	Fetal Brain Female	brain
8	chr8:63660800-63661200	Enhancers	ES-I3 Cell Line	embryonic stem cell
9	chr8:63661400-63662000	Weak transcription	Cortex derived primary cultured neurospheres	brain
10	chr8:63662000-63663600	Strong transcription	Cortex derived primary cultured neurospheres	brain
11	chr8:63662600-63664000	Strong transcription	Brain Germinal Matrix	brain
12	chr8:63663400-63663600	Enhancers	Fetal Brain Female	brain
13	chr8:63663600-63669800	Weak transcription	Cortex derived primary cultured neurospheres	brain
14	chr8:63664000-63665600	Weak transcription	Brain Germinal Matrix	brain
15	chr8:63673800-63674200	Enhancers	iPS-18 Cell Line	embryonic stem cell
16	chr8:63691800-63697200	Weak transcription	Brain Germinal Matrix	brain
17	chr8:63694400-63694800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr8:63694800-63697600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr8:63697200-63697400	Enhancers	Brain Germinal Matrix	brain
20	chr8:63697400-63698200	Weak transcription	Brain Germinal Matrix	brain
21	chr8:63697600-63698800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr8:63698000-63698600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
23	chr8:63698000-63699800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
24	chr8:63698200-63699600	Enhancers	Brain Germinal Matrix	brain
25	chr8:63698400-63699000	Enhancers	HUES48 Cell Line	embryonic stem cell
26	chr8:63698400-63699600	Enhancers	Cortex derived primary cultured neurospheres	brain
27	chr8:63698600-63699600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
28	chr8:63698600-63699800	Enhancers	iPS-18 Cell Line	embryonic stem cell
29	chr8:63699000-63699200	Enhancers	iPS-20b Cell Line	embryonic stem cell
30	chr8:63699000-63699400	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
31	chr8:63699000-63699400	Enhancers	HUES6 Cell Line	embryonic stem cell
32	chr8:63699000-63699400	Enhancers	HUES64 Cell Line	embryonic stem cell
33	chr8:63699000-63699600	Enhancers	H1 Cell Line	embryonic stem cell
34	chr8:63699000-63699800	Enhancers	iPS-15b Cell Line	embryonic stem cell
35	chr8:63699200-63699600	Enhancers	ES-I3 Cell Line	embryonic stem cell
36	chr8:63699200-63699600	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
37	chr8:63699200-63699600	Enhancers	Fetal Brain Female	brain
38	chr8:63699400-63699800	Enhancers	HUES48 Cell Line	embryonic stem cell
39	chr8:63699600-63699800	Enhancers	iPS-20b Cell Line	embryonic stem cell
40	chr8:63706800-63707200	Active TSS	Pancreatic Islets	Pancreatic Islet
41	chr8:63708800-63709800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr8:63709400-63710400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr8:63709600-63710000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr8:63710000-63710200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr8:63711000-63711400	Weak transcription	Cortex derived primary cultured neurospheres	brain
46	chr8:63712200-63712600	Active TSS	Fetal Heart	heart
47	chr8:63713000-63713600	Active TSS	HUES6 Cell Line	embryonic stem cell
48	chr8:63726000-63726800	ZNF genes & repeats	Cortex derived primary cultured neurospheres	brain
49	chr8:63726800-63731400	Weak transcription	Cortex derived primary cultured neurospheres	brain
50	chr8:63733200-63733600	Enhancers	Brain Germinal Matrix	brain

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