Variant report

Variant	nsv916637
Chromosome Location	chr8:114116303-114338450
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	chr8:114213112-114213298	H1-hESC	embryonic stem cell:	n/a	n/a
2	BRCA1	chr8:114262250-114262301	Hela-S3	cervix:	n/a	n/a
3	CEBPB	chr8:114252098-114252213	HepG2	liver:	n/a	chr8:114252167-114252178
4	CEBPB	chr8:114132330-114132582	IMR90	lung:	n/a	chr8:114132429-114132442 chr8:114132429-114132442 chr8:114132429-114132442 chr8:114132429-114132440
5	CEBPB	chr8:114205769-114206101	IMR90	lung:	n/a	chr8:114205937-114205950
6	CEBPB	chr8:114196678-114196907	A549	lung:	n/a	chr8:114196778-114196789
7	CEBPB	chr8:114212974-114213317	H1-hESC	embryonic stem cell:	n/a	chr8:114213140-114213151
8	CEBPB	chr8:114189729-114189941	HepG2	liver:	n/a	chr8:114189822-114189831 chr8:114189822-114189833
9	CEBPB	chr8:114268640-114268908	A549	lung:	n/a	chr8:114268770-114268781 chr8:114268768-114268779 chr8:114268768-114268781 chr8:114268768-114268781 chr8:114268770-114268781 chr8:114268768-114268781
10	CEBPB	chr8:114119344-114119665	HepG2	liver:	n/a	chr8:114119497-114119508 chr8:114119497-114119506
11	CEBPB	chr8:114190504-114190950	IMR90	lung:	n/a	chr8:114190756-114190767
12	CEBPB	chr8:114164228-114164448	A549	lung:	n/a	n/a
13	CEBPB	chr8:114190592-114191122	A549	lung:	n/a	chr8:114190756-114190767 chr8:114191050-114191063 chr8:114190992-114191003
14	CEBPB	chr8:114268628-114268906	Hela-S3	cervix:	n/a	chr8:114268770-114268781 chr8:114268768-114268779 chr8:114268768-114268781 chr8:114268768-114268781 chr8:114268770-114268781 chr8:114268768-114268781
15	CEBPB	chr8:114268632-114268926	HepG2	liver:	n/a	chr8:114268770-114268781 chr8:114268768-114268779 chr8:114268768-114268781 chr8:114268768-114268781 chr8:114268770-114268781 chr8:114268768-114268781
16	CEBPB	chr8:114213053-114213304	A549	lung:	n/a	chr8:114213140-114213151
17	CEBPB	chr8:114205765-114206151	Hela-S3	cervix:	n/a	chr8:114205937-114205950
18	CEBPB	chr8:114190575-114190941	HepG2	liver:	n/a	chr8:114190756-114190767
19	CEBPB	chr8:114298924-114298973	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr8:114196640-114196938	HepG2	liver:	n/a	chr8:114196778-114196789
21	CEBPB	chr8:114212978-114213328	IMR90	lung:	n/a	chr8:114213140-114213151
22	CEBPB	chr8:114190745-114190772	K562	blood:	n/a	chr8:114190756-114190767
23	CEBPB	chr8:114212976-114213326	HepG2	liver:	n/a	chr8:114213140-114213151
24	CEBPB	chr8:114190613-114191127	H1-hESC	embryonic stem cell:	n/a	chr8:114190756-114190767 chr8:114191050-114191063 chr8:114190992-114191003
25	CEBPB	chr8:114201448-114201545	A549	lung:	n/a	n/a
26	CEBPB	chr8:114190615-114190871	ECC-1	luminal epithelium:	n/a	chr8:114190756-114190767
27	CEBPB	chr8:114212994-114213313	K562	blood:	n/a	chr8:114213140-114213151
28	CEBPB	chr8:114268628-114268946	IMR90	lung:	n/a	chr8:114268770-114268781 chr8:114268768-114268779 chr8:114268768-114268781 chr8:114268768-114268781 chr8:114268770-114268781 chr8:114268768-114268781
29	CHD2	chr8:114239705-114240024	H1-hESC	embryonic stem cell:	n/a	n/a
30	CHD2	chr8:114239762-114239942	HepG2	liver:	n/a	n/a
31	CTCF	chr8:114239820-114239970	SAEC	small airway:	n/a	n/a
32	CTCF	chr8:114184060-114184210	GM12871	blood:	n/a	n/a
33	CTCF	chr8:114239900-114240050	HA-sp	spinal cord:	n/a	n/a
34	CTCF	chr8:114184080-114184230	GM12866	blood:	n/a	n/a
35	CTCF	chr8:114214360-114214510	GM12874	blood:	n/a	n/a
36	CTCF	chr8:114184120-114184270	HEEpiC	esophagus:	n/a	n/a
37	CTCF	chr8:114214468-114214924	MCF-7	breast:	n/a	chr8:114214686-114214704 chr8:114214689-114214702 chr8:114214713-114214721 chr8:114214688-114214709 chr8:114214689-114214698 chr8:114214687-114214703
38	CTCF	chr8:114239840-114239990	HCPEpiC	choroid plexus:	n/a	n/a
39	CTCF	chr8:114128280-114128430	NHEK	skin:	n/a	n/a
40	CTCF	chr8:114214600-114214750	SAEC	small airway:	n/a	chr8:114214686-114214704 chr8:114214689-114214702 chr8:114214713-114214721 chr8:114214688-114214709 chr8:114214689-114214698 chr8:114214687-114214703
41	CTCF	chr8:114214570-114214797	GM13977	blood:	n/a	chr8:114214686-114214704 chr8:114214689-114214702 chr8:114214713-114214721 chr8:114214688-114214709 chr8:114214689-114214698 chr8:114214687-114214703
42	CTCF	chr8:114216832-114216877	MCF-7	breast:	n/a	n/a
43	CTCF	chr8:114214640-114214790	HMEC	breast:	n/a	chr8:114214686-114214704 chr8:114214689-114214702 chr8:114214713-114214721 chr8:114214688-114214709 chr8:114214689-114214698 chr8:114214687-114214703
44	CTCF	chr8:114184100-114184250	HAc	cerebellar:	n/a	n/a
45	CTCF	chr8:114214600-114214750	HEEpiC	esophagus:	n/a	chr8:114214686-114214704 chr8:114214689-114214702 chr8:114214713-114214721 chr8:114214688-114214709 chr8:114214689-114214698 chr8:114214687-114214703
46	CTCF	chr8:114214680-114214830	HCT-116	colon:	n/a	chr8:114214686-114214704 chr8:114214689-114214702 chr8:114214713-114214721 chr8:114214688-114214709 chr8:114214689-114214698 chr8:114214687-114214703
47	CTCF	chr8:114239899-114239963	GM12878	blood:	n/a	n/a
48	CTCF	chr8:114184100-114184250	HRE	kidney:	n/a	n/a
49	CTCF	chr8:114214630-114214740	GM10266	blood:	n/a	chr8:114214686-114214704 chr8:114214689-114214702 chr8:114214713-114214721 chr8:114214688-114214709 chr8:114214689-114214698 chr8:114214687-114214703
50	CTCF	chr8:114214600-114214750	GM12873	blood:	n/a	chr8:114214686-114214704 chr8:114214689-114214702 chr8:114214713-114214721 chr8:114214688-114214709 chr8:114214689-114214698 chr8:114214687-114214703

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:114133190-114133240	ECC-1	luminal epithelium:	n/a
2	chr8:114133190-114133240	H1-hESC	embryonic stem cell:	embryo
3	chr8:114133190-114133240	GM12878	blood:	n/a
4	chr8:114133190-114133240	HCM	heart:	n/a
5	chr8:114133190-114133240	MCF-7	breast:	n/a
6	chr8:114133190-114133240	HRCEpiC	kidney:	n/a
7	chr8:114133190-114133240	AG10803	skin:	n/a
8	chr8:114133190-114133240	NB4	blood:	n/a
9	chr8:114133190-114133240	AG04450	lung:	fetal
10	chr8:114133190-114133240	PrEC	prostate:	n/a
11	chr8:114133190-114133240	HepG2	liver:	n/a
12	chr8:114133190-114133240	K562	blood:	n/a
13	chr8:114133190-114133240	AG09309	skin:	n/a
14	chr8:114133190-114133240	PFSK-1	brain:	n/a
15	chr8:114133190-114133240	HNPCEpiC	eye:	n/a
16	chr8:114133190-114133240	HRE	kidney:	n/a
17	chr8:114133190-114133240	HEK293	kidney:	embryo
18	chr8:114133190-114133240	Jurkat	blood:	n/a
19	chr8:114133190-114133240	HPAEpiC	pulmonary alveolar:	n/a
20	chr8:114133190-114133240	T-47D	breast:	n/a
21	chr8:114133190-114133240	SKMC	muscle:	n/a
22	chr8:114133190-114133240	GM12892	blood:	n/a
23	chr8:114133190-114133240	HCT-116	colon:	n/a
24	chr8:114133190-114133240	PANC-1	pancreas:	n/a
25	chr8:114133190-114133240	SAEC	small airway:	n/a
26	chr8:114133190-114133240	CMK	blood:	n/a
27	chr8:114133190-114133240	NHBE	bronchial:	n/a
28	chr8:114133190-114133240	BJ	skin:	n/a
29	chr8:114133190-114133240	HAEpiC	amniotic membrane:	n/a
30	chr8:114133190-114133240	Caco-2	colon:	n/a
31	chr8:114133190-114133240	ProgFib	skin:	n/a
32	chr8:114133190-114133240	AG09319	gingival:	n/a
33	chr8:114133190-114133240	SK-N-SH_RA	brain:	n/a
34	chr8:114133190-114133240	GM12891	blood:	n/a
35	chr8:114133190-114133240	NHDF-neo	bronchial:	n/a
36	chr8:114133190-114133240	NH-A	brain:	n/a
37	chr8:114133190-114133240	RPTEC	kidney:	n/a
38	chr8:114133190-114133240	HCF	heart:	n/a
39	chr8:114133190-114133240	HL-60	blood:	n/a
40	chr8:114133190-114133240	U87	brain:	n/a
41	chr8:114133190-114133240	Hepatocyte	liver:	n/a
42	chr8:114133190-114133240	LNCaP	prostate:	n/a
43	chr8:114133190-114133240	Hela-S3	cervix:	n/a
44	chr8:114133190-114133240	HRPEpiC	eye:	n/a
45	chr8:114133190-114133240	AoSMC	blood vessel:	n/a
46	chr8:114133190-114133240	ovcar-3	ovarian:	n/a
47	chr8:114133190-114133240	A549	lung:	n/a
48	chr8:114133190-114133240	HEEpiC	esophagus:	n/a
49	chr8:114133190-114133240	HMEC	breast:	n/a
50	chr8:114133190-114133240	GM19239	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr8:114229145..114230999-chr8:114232153..114234565,2	K562	blood:
2	chr8:114189275..114190202-chr8:114449887..114450479,2	MCF-7	breast:
3	chr8:113773909..113774597-chr8:114183855..114184506,4	MCF-7	breast:
4	chr8:114229145..114230999-chr8:114232153..114234565,2	K562	blood:
5	chr8:113773910..113774788-chr8:114210759..114211408,2	MCF-7	breast:
6	chr1:51721667..51722414-chr8:114314203..114314730,2	MCF-7	breast:
7	chr8:114214112..114215316-chr8:114390224..114391492,6	MCF-7	breast:
8	chr8:114200013..114203361-chr8:114205851..114208683,3	K562	blood:
9	chr8:114143657..114145311-chr8:114151468..114153338,2	MCF-7	breast:
10	chr8:114145284..114147618-chr8:114150082..114152727,2	K562	blood:
11	chr16:73534459..73535268-chr8:114328120..114328877,2	MCF-7	breast:
12	chr8:114143657..114145311-chr8:114151468..114153338,2	MCF-7	breast:
13	chr8:114189402..114189999-chr8:114390956..114391473,2	MCF-7	breast:
14	chr8:113812932..113813631-chr8:114183972..114184626,2	MCF-7	breast:
15	chr8:114145284..114147618-chr8:114150082..114152727,2	K562	blood:
16	chr8:114228732..114230731-chr8:114233226..114235418,2	MCF-7	breast:
17	chr8:114228732..114230731-chr8:114233226..114235418,2	MCF-7	breast:
18	chr3:157419711..157420339-chr8:114148761..114149283,2	MCF-7	breast:
19	chr8:114200013..114203361-chr8:114205851..114208683,3	K562	blood:
20	chr8:113813041..113814009-chr8:114183692..114184450,5	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TRPS1-4	chr8:114321434-114327022	NONHSAT128345

Variant related genes	Relation type
CSMD3	TF binding region
CSMD3	CpG island

Extended variants
information (count: 1714 )
Associated
traits (count: 105 )

Variant overlapped rSNPs/rCNVs (count:1714 , 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	rs564705760	chr8:114116313-114116314	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs149673395	chr8:114116322-114116323	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs376850396	chr8:114116361-114116362	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs570314693	chr8:114116388-114116389	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs535849684	chr8:114116508-114116509	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs371168949	chr8:114116526-114116527	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs541570951	chr8:114116541-114116542	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs549071751	chr8:114116554-114116555	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs566186871	chr8:114116578-114116579	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs560593296	chr8:114116589-114116590	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs145504262	chr8:114116604-114116605	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs557821053	chr8:114116623-114116624	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs1354445	chr8:114116670-114116671	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs75493024	chr8:114116680-114116681	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs1402940	chr8:114116686-114116687	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs573821772	chr8:114116687-114116688	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs542631766	chr8:114116783-114116784	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs141777016	chr8:114116795-114116796	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs531945933	chr8:114116853-114116854	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs78716274	chr8:114116920-114116921	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs183564619	chr8:114116973-114116974	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs544814450	chr8:114116976-114116977	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs148854550	chr8:114116977-114116978	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs551719907	chr8:114117119-114117120	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs533566976	chr8:114117151-114117152	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs543991426	chr8:114117165-114117166	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs563986460	chr8:114117168-114117169	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs571946815	chr8:114117178-114117179	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs549630081	chr8:114117219-114117220	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs117665504	chr8:114117272-114117273	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs374206183	chr8:114117333-114117334	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs199710071	chr8:114117340-114117341	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs528483037	chr8:114117350-114117351	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs554199179	chr8:114117411-114117412	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs35263275	chr8:114117468-114117469	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs74539006	chr8:114117470-114117471	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs188393941	chr8:114117483-114117484	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs537977155	chr8:114117507-114117508	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs536864665	chr8:114117548-114117549	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs556711154	chr8:114117554-114117555	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs567434331	chr8:114117583-114117584	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs536190711	chr8:114117605-114117606	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs77036880	chr8:114117609-114117610	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs34927606	chr8:114117621-114117622	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs572794775	chr8:114117625-114117626	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs556990589	chr8:114117649-114117650	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs544972048	chr8:114117688-114117689	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs146975875	chr8:114117700-114117701	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs575373817	chr8:114117804-114117805	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs544050561	chr8:114117817-114117818	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:105)

Disease	PMID	Source
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
Gastric cancer	17908304	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Liver carcinoma	19366792	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	17603634	CNVD
Testicular cancer	18059402	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
abnormal development	18461090	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
Glioblastoma multiforme	21080181	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
Cancer	16751803	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
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	21399628	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	17393978	CNVD
Burkitt''s lymphoma	18698080	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Colorectal cancer	16774939	CNVD
Autosomal-dominant progressive external ophthalmoplegia	19664747	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Sezary syndrome	18413736	CNVD
Breast cancer	21611746	CNVD
Developmental delay	21147756	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Non-small cell lung cancer	19010865	CNVD
small cell lung cancer	20016488	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21364760	CNVD
Neuroticism	17667963	CNVD
Papillary thyroid cancer	17515504	CNVD
Basal cell lymphoma	17053054	CNVD
Schizophrenia	20967226	CNVD
Prostate cancer	22341455	CNVD
Colorectal cancer	21645411	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD
Breast cancer	22522925	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Renal cell carcinoma	21215367	CNVD

Chromatin state (count:112 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:114115800-114117400	Enhancers	HUVEC	blood vessel
2	chr8:114116200-114116600	Enhancers	Dnd41	blood
3	chr8:114116200-114117600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr8:114117400-114117600	Flanking Active TSS	HUVEC	blood vessel
5	chr8:114117400-114118000	Enhancers	Fetal Intestine Small	intestine
6	chr8:114117600-114117800	Enhancers	HUVEC	blood vessel
7	chr8:114117600-114118000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr8:114117800-114118000	Flanking Active TSS	HUVEC	blood vessel
9	chr8:114118000-114118800	Enhancers	HUVEC	blood vessel
10	chr8:114129400-114132800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
11	chr8:114129600-114129800	ZNF genes & repeats	Brain Germinal Matrix	brain
12	chr8:114129800-114130200	ZNF genes & repeats	Brain Substantia Nigra	brain
13	chr8:114129800-114132800	Weak transcription	Brain Germinal Matrix	brain
14	chr8:114130200-114133400	Weak transcription	Brain Substantia Nigra	brain
15	chr8:114132000-114133800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr8:114132400-114133800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr8:114132800-114133600	Enhancers	Brain Germinal Matrix	brain
18	chr8:114132800-114133600	Enhancers	Brain Inferior Temporal Lobe	brain
19	chr8:114132800-114133800	Enhancers	HUES48 Cell Line	embryonic stem cell
20	chr8:114132800-114133800	Enhancers	Dnd41	blood
21	chr8:114132800-114134000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
22	chr8:114132800-114134000	Enhancers	HUES64 Cell Line	embryonic stem cell
23	chr8:114133000-114133200	Enhancers	iPS-18 Cell Line	embryonic stem cell
24	chr8:114133000-114133600	Enhancers	iPS-15b Cell Line	embryonic stem cell
25	chr8:114133000-114133800	Enhancers	ES-I3 Cell Line	embryonic stem cell
26	chr8:114133000-114133800	Enhancers	HUES6 Cell Line	embryonic stem cell
27	chr8:114133200-114133600	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
28	chr8:114133200-114133600	Enhancers	Brain Angular Gyrus	brain
29	chr8:114133200-114133800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr8:114133200-114133800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
31	chr8:114133200-114133800	Enhancers	iPS-20b Cell Line	embryonic stem cell
32	chr8:114133200-114133800	Enhancers	Cortex derived primary cultured neurospheres	brain
33	chr8:114133400-114133800	Active TSS	Brain Substantia Nigra	brain
34	chr8:114133600-114133800	Enhancers	iPS-18 Cell Line	embryonic stem cell
35	chr8:114154600-114154800	Enhancers	Brain Substantia Nigra	brain
36	chr8:114156600-114157400	Enhancers	Brain Hippocampus Middle	brain
37	chr8:114156600-114157400	Enhancers	Brain Substantia Nigra	brain
38	chr8:114157200-114157600	Enhancers	Brain Anterior Caudate	brain
39	chr8:114165400-114165600	Enhancers	Dnd41	blood
40	chr8:114165600-114166800	Weak transcription	Dnd41	blood
41	chr8:114166800-114167800	Enhancers	Dnd41	blood
42	chr8:114167800-114168000	Flanking Active TSS	Dnd41	blood
43	chr8:114168000-114168200	Enhancers	Dnd41	blood
44	chr8:114168200-114168400	Flanking Active TSS	Dnd41	blood
45	chr8:114168400-114170600	Enhancers	Dnd41	blood
46	chr8:114176000-114178200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
47	chr8:114176800-114177400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr8:114177000-114177400	Enhancers	H1 Cell Line	embryonic stem cell
49	chr8:114177000-114177400	Enhancers	iPS-15b Cell Line	embryonic stem cell
50	chr8:114182000-114182400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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