Variant report

Variant	nsv1016814
Chromosome Location	chr8:4630807-4667096
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:110)
CpG islands
(count:183)
Chromatin interactive
region (count:0)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:110 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CHD2	chr8:4644622-4644850	H1-hESC	embryonic stem cell:	n/a	n/a
2	CHD2	chr8:4654890-4654920	HepG2	liver:	n/a	n/a
3	CTCF	chr8:4644620-4644770	RPTEC	kidney:	n/a	n/a
4	CTCF	chr8:4644660-4644810	GM12868	blood:	n/a	n/a
5	CTCF	chr8:4644680-4644830	SK-N-SH_RA	brain:	n/a	n/a
6	CTCF	chr8:4644700-4644850	HRE	kidney:	n/a	n/a
7	CTCF	chr8:4644625-4644807	SK-N-SH_RA	brain:	n/a	n/a
8	CTCF	chr8:4644540-4644690	HFF-Myc	foreskin:	n/a	n/a
9	CTCF	chr8:4644620-4644770	WERI-Rb-1	eye:	n/a	n/a
10	CTCF	chr8:4644600-4644750	WERI-Rb-1	eye:	n/a	n/a
11	CTCF	chr8:4644660-4644810	K562	blood:	n/a	n/a
12	CTCF	chr8:4644611-4644850	H1-hESC	embryonic stem cell:	n/a	n/a
13	CTCF	chr8:4644587-4644847	H1-hESC	embryonic stem cell:	n/a	n/a
14	CTCF	chr8:4644640-4644790	GM12874	blood:	n/a	n/a
15	CTCF	chr8:4644584-4644870	K562	blood:	n/a	n/a
16	CTCF	chr8:4644647-4644794	SK-N-SH_RA	brain:	n/a	n/a
17	CTCF	chr8:4644551-4644864	K562	blood:	n/a	n/a
18	CTCF	chr8:4644516-4644932	H1-hESC	embryonic stem cell:	n/a	n/a
19	CTCF	chr8:4644640-4644790	GM12865	blood:	n/a	n/a
20	CTCF	chr8:4644640-4644790	HepG2	liver:	n/a	n/a
21	CTCF	chr8:4644646-4644815	A549	lung:	n/a	n/a
22	CTCF	chr8:4644640-4644790	GM12868	blood:	n/a	n/a
23	CTCF	chr8:4644600-4644750	GM12872	blood:	n/a	n/a
24	CTCF	chr8:4644660-4644810	HepG2	liver:	n/a	n/a
25	CTCF	chr8:4632207-4632286	Lung_OC	lung:	n/a	n/a
26	CTCF	chr8:4644600-4644750	SAEC	small airway:	n/a	n/a
27	CTCF	chr8:4644640-4644790	HBMEC	blood vessel:	n/a	n/a
28	CTCF	chr8:4644700-4644850	GM12869	blood:	n/a	n/a
29	CTCF	chr8:4644647-4644806	GM12891	blood:	n/a	n/a
30	CTCF	chr8:4650026-4650077	ProgFib	skin:	n/a	n/a
31	CTCF	chr8:4644700-4644850	GM12875	blood:	n/a	n/a
32	CTCF	chr8:4644660-4644810	GM12866	blood:	n/a	n/a
33	CTCF	chr8:4644652-4644813	HepG2	liver:	n/a	n/a
34	CTCF	chr8:4644640-4644790	A549	lung:	n/a	n/a
35	CTCF	chr8:4644680-4644830	GM12871	blood:	n/a	n/a
36	CTCF	chr8:4644620-4644770	NB4	blood:	n/a	n/a
37	CTCF	chr8:4644600-4644750	HEK293	kidney:	n/a	n/a
38	CTCF	chr8:4644658-4644814	Gliobla	brain:	n/a	n/a
39	CTCF	chr8:4644591-4644910	K562	blood:	n/a	n/a
40	CTCF	chr8:4644640-4644790	GM12872	blood:	n/a	n/a
41	CTCF	chr8:4644620-4644770	GM12872	blood:	n/a	n/a
42	CTCF	chr8:4644620-4644770	SAEC	small airway:	n/a	n/a
43	CTCF	chr8:4644680-4644748	Pancreas_OC	pancreas:	n/a	n/a
44	CTCF	chr8:4644640-4644790	HEK293	kidney:	n/a	n/a
45	CTCF	chr8:4654887-4654940	Spleen_OC	spleen:	n/a	n/a
46	CTCF	chr8:4644600-4644750	GM12873	blood:	n/a	n/a
47	CTCF	chr8:4644700-4644850	Caco-2	colon:	n/a	n/a
48	CTCF	chr8:4644642-4644821	K562	blood:	n/a	n/a
49	CTCF	chr8:4644660-4644810	Hela-S3	cervix:	n/a	n/a
50	CTCF	chr8:4644672-4644761	GM13977	blood:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:4644719-4644769	PANC-1	pancreas:	n/a
2	chr8:4644719-4644769	HRPEpiC	eye:	n/a
3	chr8:4644739-4644789	CMK	blood:	n/a
4	chr8:4644719-4644769	HIPEpiC	eye:	n/a
5	chr8:4637584-4637634	HepG2	liver:	n/a
6	chr8:4637584-4637634	HCM	heart:	n/a
7	chr8:4644739-4644789	HAEpiC	amniotic membrane:	n/a
8	chr8:4637584-4637634	MCF-7	breast:	n/a
9	chr8:4644719-4644769	HMEC	breast:	n/a
10	chr8:4637584-4637634	RPTEC	kidney:	n/a
11	chr8:4644739-4644789	AG09309	skin:	n/a
12	chr8:4637584-4637634	BJ	skin:	n/a
13	chr8:4644739-4644789	ProgFib	skin:	n/a
14	chr8:4644739-4644789	SK-N-SH	brain:	n/a
15	chr8:4644719-4644769	SKMC	muscle:	n/a
16	chr8:4644719-4644769	AoSMC	blood vessel:	n/a
17	chr8:4644739-4644789	LNCaP	prostate:	n/a
18	chr8:4644719-4644769	HepG2	liver:	n/a
19	chr8:4637584-4637634	HNPCEpiC	eye:	n/a
20	chr8:4644719-4644769	NHDF-neo	bronchial:	n/a
21	chr8:4644719-4644769	GM12892	blood:	n/a
22	chr8:4637584-4637634	K562	blood:	n/a
23	chr8:4644719-4644769	ProgFib	skin:	n/a
24	chr8:4637584-4637634	HRCEpiC	kidney:	n/a
25	chr8:4637584-4637634	NH-A	brain:	n/a
26	chr8:4637584-4637634	SKMC	muscle:	n/a
27	chr8:4644739-4644789	HEK293	kidney:	embryo
28	chr8:4644739-4644789	NB4	blood:	n/a
29	chr8:4637584-4637634	AG09319	gingival:	n/a
30	chr8:4644739-4644789	HRPEpiC	eye:	n/a
31	chr8:4644739-4644789	RPTEC	kidney:	n/a
32	chr8:4644739-4644789	NHDF-neo	bronchial:	n/a
33	chr8:4644719-4644769	HNPCEpiC	eye:	n/a
34	chr8:4637584-4637634	HL-60	blood:	n/a
35	chr8:4644739-4644789	Caco-2	colon:	n/a
36	chr8:4644719-4644769	GM12891	blood:	n/a
37	chr8:4644739-4644789	NHBE	bronchial:	n/a
38	chr8:4644719-4644769	GM19239	blood:	n/a
39	chr8:4644719-4644769	HUVEC	blood vessel:	n/a
40	chr8:4637584-4637634	HCPEpiC	choroid plexus:	n/a
41	chr8:4644739-4644789	AG10803	skin:	n/a
42	chr8:4644739-4644789	HRE	kidney:	n/a
43	chr8:4644719-4644769	HPAEpiC	pulmonary alveolar:	n/a
44	chr8:4644739-4644789	HEEpiC	esophagus:	n/a
45	chr8:4644739-4644789	HCM	heart:	n/a
46	chr8:4637584-4637634	U87	brain:	n/a
47	chr8:4637584-4637634	BE2_C	brain:	n/a
48	chr8:4637584-4637634	A549	lung:	n/a
49	chr8:4644719-4644769	HRE	kidney:	n/a
50	chr8:4644719-4644769	BJ	skin:	n/a

No data

(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: 1880 )
Associated
traits (count: 125 )

Variant overlapped rSNPs/rCNVs (count:1880 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs191715021	chr8:4630837-4630838	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs112935976	chr8:4630840-4630841	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs75634845	chr8:4630846-4630847	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs189270162	chr8:4630853-4630854	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs76334563	chr8:4630859-4630860	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs529526968	chr8:4630860-4630861	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs547015023	chr8:4630868-4630869	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs180698874	chr8:4630876-4630877	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs532901924	chr8:4630879-4630880	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs551147184	chr8:4630882-4630883	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs187228412	chr8:4630901-4630902	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs369546600	chr8:4630906-4630907	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs150858363	chr8:4630914-4630915	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs190605534	chr8:4630920-4630921	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs567603870	chr8:4630925-4630926	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs9644369	chr8:4630930-4630931	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs554256409	chr8:4630955-4630956	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs572463829	chr8:4630957-4630958	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs67990550	chr8:4630960-4630961	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs181712679	chr8:4630975-4630976	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs185784279	chr8:4630978-4630979	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs543688323	chr8:4631000-4631001	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs12548690	chr8:4631002-4631003	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs370996737	chr8:4631015-4631016	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs574038962	chr8:4631022-4631023	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs541314796	chr8:4631056-4631057	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs190241930	chr8:4631057-4631058	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs10091902	chr8:4631106-4631107	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs551477014	chr8:4631107-4631108	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs563205658	chr8:4631122-4631123	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs530615407	chr8:4631128-4631129	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs373992128	chr8:4631133-4631134	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs548934821	chr8:4631141-4631142	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs182606978	chr8:4631154-4631155	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs534958537	chr8:4631160-4631161	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs546876801	chr8:4631165-4631166	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs566099587	chr8:4631189-4631190	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs139138439	chr8:4631212-4631213	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs149941637	chr8:4631241-4631242	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs535652953	chr8:4631242-4631243	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs17347502	chr8:4631249-4631250	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
42	rs548947458	chr8:4631253-4631254	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs555578243	chr8:4631276-4631277	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs573853090	chr8:4631297-4631298	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs541327290	chr8:4631363-4631364	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs13256305	chr8:4631405-4631406	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs79681206	chr8:4631409-4631410	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs544715306	chr8:4631442-4631443	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs147640409	chr8:4631455-4631456	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs530569754	chr8:4631456-4631457	Weak transcription Enhancers	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:52 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:4625200-4631400	Weak transcription	Brain Angular Gyrus	brain
2	chr8:4630800-4631200	Enhancers	Cortex derived primary cultured neurospheres	brain
3	chr8:4630800-4631200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr8:4630800-4631200	Active TSS	Brain Anterior Caudate	brain
5	chr8:4630800-4631200	Active TSS	Brain Hippocampus Middle	brain
6	chr8:4630800-4631200	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
7	chr8:4630800-4637000	Weak transcription	Brain Cingulate Gyrus	brain
8	chr8:4631200-4631600	Enhancers	Brain Inferior Temporal Lobe	brain
9	chr8:4631200-4632400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr8:4631400-4631600	Enhancers	Brain Angular Gyrus	brain
11	chr8:4631600-4638800	Weak transcription	Brain Angular Gyrus	brain
12	chr8:4632200-4632600	Enhancers	HUES48 Cell Line	embryonic stem cell
13	chr8:4635800-4636800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr8:4636000-4636200	Enhancers	Fetal Kidney	kidney
15	chr8:4636200-4637000	Weak transcription	Fetal Kidney	kidney
16	chr8:4636600-4639000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
17	chr8:4636800-4638000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr8:4637000-4637800	Enhancers	Rectal Smooth Muscle	rectum
19	chr8:4637000-4638000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr8:4637000-4638000	Enhancers	Brain Cingulate Gyrus	brain
21	chr8:4637000-4638600	Enhancers	Fetal Kidney	kidney
22	chr8:4637000-4639000	Enhancers	Cortex derived primary cultured neurospheres	brain
23	chr8:4637200-4637600	Enhancers	Fetal Brain Female	brain
24	chr8:4637200-4637800	Enhancers	Fetal Brain Male	brain
25	chr8:4637200-4638000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
26	chr8:4637200-4638000	Enhancers	Colon Smooth Muscle	Colon
27	chr8:4637200-4639000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr8:4637400-4638000	Enhancers	Fetal Stomach	stomach
29	chr8:4637600-4638800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr8:4638000-4638400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr8:4638000-4639000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
32	chr8:4638000-4639200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr8:4638000-4639600	Weak transcription	Brain Cingulate Gyrus	brain
34	chr8:4638400-4639000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr8:4638800-4639400	Enhancers	Brain Angular Gyrus	brain
36	chr8:4639000-4640800	Weak transcription	Cortex derived primary cultured neurospheres	brain
37	chr8:4639000-4641000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
38	chr8:4639200-4639400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
39	chr8:4639400-4640600	Weak transcription	Brain Angular Gyrus	brain
40	chr8:4639600-4639800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr8:4639600-4639800	Enhancers	Brain Cingulate Gyrus	brain
42	chr8:4640600-4640800	Enhancers	Brain Angular Gyrus	brain
43	chr8:4640800-4641400	Enhancers	Cortex derived primary cultured neurospheres	brain
44	chr8:4641000-4641200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr8:4641000-4641400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
46	chr8:4644400-4645000	Enhancers	HUES48 Cell Line	embryonic stem cell
47	chr8:4644600-4644800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
48	chr8:4653200-4654000	Enhancers	HUES6 Cell Line	embryonic stem cell
49	chr8:4653200-4654400	Enhancers	HUES48 Cell Line	embryonic stem cell
50	chr8:4653800-4654200	Enhancers	H9 Cell Line	embryonic stem cell

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