Variant report

Variant	nsv539636
Chromosome Location	chr8:63275987-63439650
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:472)
CpG islands
(count:305)
Chromatin interactive
region (count:27)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:472 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:63435769-63436270	HepG2	liver:	n/a	n/a
2	ARID3A	chr8:63374900-63374966	HepG2	liver:	n/a	n/a
3	ATF1	chr8:63421756-63421925	K562	blood:	n/a	n/a
4	BACH1	chr8:63275787-63275988	H1-hESC	embryonic stem cell:	n/a	chr8:63275840-63275854
5	BCL11A	chr8:63385596-63385878	GM12878	blood:	n/a	n/a
6	BCL3	chr8:63435720-63436281	A549	lung:	n/a	n/a
7	BHLHE40	chr8:63385606-63385742	GM12878	blood:	n/a	n/a
8	CBX3	chr8:63415983-63416273	K562	blood:	n/a	n/a
9	CCNT2	chr8:63308137-63308337	K562	blood:	n/a	n/a
10	CEBPB	chr8:63276341-63276676	IMR90	lung:	n/a	chr8:63276657-63276665 chr8:63276493-63276504 chr8:63276494-63276503 chr8:63276494-63276503 chr8:63276494-63276503 chr8:63276492-63276505 chr8:63276494-63276503
11	CEBPB	chr8:63276349-63276575	K562	blood:	n/a	chr8:63276493-63276504 chr8:63276494-63276503 chr8:63276494-63276503 chr8:63276494-63276503 chr8:63276492-63276505 chr8:63276494-63276503
12	CEBPB	chr8:63337971-63338145	A549	lung:	n/a	chr8:63338032-63338043
13	CEBPB	chr8:63418397-63418745	IMR90	lung:	n/a	n/a
14	CEBPB	chr8:63276340-63276647	A549	lung:	n/a	chr8:63276493-63276504 chr8:63276494-63276503 chr8:63276494-63276503 chr8:63276494-63276503 chr8:63276492-63276505 chr8:63276494-63276503
15	CEBPB	chr8:63381816-63381998	A549	lung:	n/a	chr8:63381841-63381852
16	CEBPB	chr8:63435809-63436173	A549	lung:	n/a	n/a
17	CEBPB	chr8:63402982-63403185	HepG2	liver:	n/a	chr8:63403061-63403072
18	CEBPB	chr8:63435813-63436186	HepG2	liver:	n/a	n/a
19	CEBPB	chr8:63337890-63338193	HepG2	liver:	n/a	chr8:63338032-63338043
20	CEBPB	chr8:63435646-63436271	MCF-7	breast:	n/a	n/a
21	CEBPB	chr8:63418482-63418719	A549	lung:	n/a	n/a
22	CEBPB	chr8:63436941-63437400	MCF-7	breast:	n/a	n/a
23	CEBPB	chr8:63431742-63431833	A549	lung:	n/a	n/a
24	CEBPB	chr8:63334351-63334505	HepG2	liver:	n/a	n/a
25	CEBPB	chr8:63435598-63436346	MCF-7	breast:	n/a	n/a
26	CEBPB	chr8:63368097-63368297	HepG2	liver:	n/a	chr8:63368175-63368186
27	CEBPB	chr8:63381751-63381991	HepG2	liver:	n/a	chr8:63381841-63381852
28	CEBPB	chr8:63290342-63290513	HepG2	liver:	n/a	chr8:63290430-63290441
29	CEBPB	chr8:63280767-63281064	IMR90	lung:	n/a	chr8:63280896-63280907
30	CEBPB	chr8:63276352-63276674	HepG2	liver:	n/a	chr8:63276657-63276665 chr8:63276493-63276504 chr8:63276494-63276503 chr8:63276494-63276503 chr8:63276494-63276503 chr8:63276492-63276505 chr8:63276494-63276503
31	CEBPB	chr8:63435779-63436222	A549	lung:	n/a	n/a
32	CEBPB	chr8:63435732-63436260	A549	lung:	n/a	n/a
33	CEBPB	chr8:63280751-63281072	A549	lung:	n/a	chr8:63280896-63280907
34	CEBPB	chr8:63280742-63281033	HepG2	liver:	n/a	chr8:63280896-63280907
35	CHD2	chr8:63287865-63287898	GM12878	blood:	n/a	n/a
36	CTCF	chr8:63317780-63317930	GM12864	blood:	n/a	n/a
37	CTCF	chr8:63317701-63317944	MCF-7	breast:	n/a	n/a
38	CTCF	chr8:63317720-63317870	GM12872	blood:	n/a	n/a
39	CTCF	chr8:63317720-63317870	HAc	cerebellar:	n/a	n/a
40	CTCF	chr8:63317760-63317910	HRPEpiC	eye:	n/a	n/a
41	CTCF	chr8:63317780-63317930	GM12872	blood:	n/a	n/a
42	CTCF	chr8:63317720-63317870	GM12870	blood:	n/a	n/a
43	CTCF	chr8:63317780-63317930	GM06990	blood:	n/a	n/a
44	CTCF	chr8:63290300-63290450	HPF	lung:	n/a	n/a
45	CTCF	chr8:63436360-63436429	Fibrobl	skin:	n/a	n/a
46	CTCF	chr8:63317660-63317810	GM12878	blood:	n/a	n/a
47	CTCF	chr8:63317771-63317875	GM13977	blood:	n/a	n/a
48	CTCF	chr8:63317742-63317912	Hela-S3	cervix:	n/a	n/a
49	CTCF	chr8:63317740-63317890	HPF	lung:	n/a	n/a
50	CTCF	chr8:63290248-63290369	LNCaP	prostate:	n/a	n/a

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:63403502-63403552	SAEC	small airway:	n/a
2	chr8:63307749-63307799	SKMC	muscle:	n/a
3	chr8:63385433-63385483	PrEC	prostate:	n/a
4	chr8:63403502-63403552	NHDF-neo	bronchial:	n/a
5	chr8:63307589-63307639	HCPEpiC	choroid plexus:	n/a
6	chr8:63403502-63403552	BJ	skin:	n/a
7	chr8:63438306-63438356	NT2-D1	testis:	n/a
8	chr8:63307749-63307799	HRPEpiC	eye:	n/a
9	chr8:63385433-63385483	IMR90	lung:	fetal
10	chr8:63307589-63307639	IMR90	lung:	fetal
11	chr8:63403502-63403552	HCPEpiC	choroid plexus:	n/a
12	chr8:63385433-63385483	HEK293	kidney:	embryo
13	chr8:63438306-63438356	PANC-1	pancreas:	n/a
14	chr8:63307589-63307639	PFSK-1	brain:	n/a
15	chr8:63385433-63385483	Caco-2	colon:	n/a
16	chr8:63307749-63307799	NB4	blood:	n/a
17	chr8:63438306-63438356	AG04449	skin:	fetal
18	chr8:63307749-63307799	NHDF-neo	bronchial:	n/a
19	chr8:63307589-63307639	PrEC	prostate:	n/a
20	chr8:63307749-63307799	PANC-1	pancreas:	n/a
21	chr8:63307589-63307639	NB4	blood:	n/a
22	chr8:63307589-63307639	GM06990	blood:	n/a
23	chr8:63385433-63385483	SK-N-SH_RA	brain:	n/a
24	chr8:63307589-63307639	LNCaP	prostate:	n/a
25	chr8:63385433-63385483	NB4	blood:	n/a
26	chr8:63307749-63307799	GM12891	blood:	n/a
27	chr8:63385433-63385483	GM12891	blood:	n/a
28	chr8:63307749-63307799	NT2-D1	testis:	n/a
29	chr8:63307749-63307799	HEEpiC	esophagus:	n/a
30	chr8:63385433-63385483	HL-60	blood:	n/a
31	chr8:63385433-63385483	Hepatocyte	liver:	n/a
32	chr8:63385433-63385483	NHBE	bronchial:	n/a
33	chr8:63385433-63385483	GM19239	blood:	n/a
34	chr8:63403502-63403552	GM19239	blood:	n/a
35	chr8:63403502-63403552	GM12878	blood:	n/a
36	chr8:63307749-63307799	HRE	kidney:	n/a
37	chr8:63438306-63438356	GM12878	blood:	n/a
38	chr8:63307749-63307799	HPAEpiC	pulmonary alveolar:	n/a
39	chr8:63307589-63307639	MCF-7	breast:	n/a
40	chr8:63403502-63403552	HCF	heart:	n/a
41	chr8:63307749-63307799	SK-N-MC	brain:	n/a
42	chr8:63307589-63307639	HCM	heart:	n/a
43	chr8:63307589-63307639	AoSMC	blood vessel:	n/a
44	chr8:63403502-63403552	HRPEpiC	eye:	n/a
45	chr8:63438306-63438356	HEEpiC	esophagus:	n/a
46	chr8:63403502-63403552	RPTEC	kidney:	n/a
47	chr8:63385433-63385483	ECC-1	luminal epithelium:	n/a
48	chr8:63385433-63385483	AG10803	skin:	n/a
49	chr8:63385433-63385483	HCM	heart:	n/a
50	chr8:63385433-63385483	HEEpiC	esophagus:	n/a

(count:27 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:63355392..63357928-chr8:63359748..63362199,2	K562	blood:
2	chr21:46294976..46295889-chr8:63408636..63409252,2	MCF-7	breast:
3	chr8:63280878..63284523-chr8:63286682..63289444,3	MCF-7	breast:
4	chr8:63318987..63320777-chr8:63321010..63323348,2	K562	blood:
5	chr8:63411360..63415299-chr8:63422885..63426744,3	K562	blood:
6	chr8:63414123..63416933-chr8:63426622..63428263,2	MCF-7	breast:
7	chr8:63295025..63297030-chr8:63298219..63300648,2	K562	blood:
8	chr8:63052210..63052840-chr8:63317439..63317973,2	MCF-7	breast:
9	chr8:63319277..63321241-chr8:63321848..63324051,2	K562	blood:
10	chr8:63280878..63284523-chr8:63286682..63289444,3	MCF-7	breast:
11	chr8:63378897..63381630-chr8:63394009..63396147,2	K562	blood:
12	chr8:63153468..63155828-chr8:63369225..63371318,2	MCF-7	breast:
13	chr8:63043534..63044140-chr8:63317610..63318142,2	MCF-7	breast:
14	chr8:63318987..63320777-chr8:63321010..63323348,2	K562	blood:
15	chr8:63355392..63357928-chr8:63359748..63362199,2	K562	blood:
16	chr8:63277582..63279518-chr8:63281007..63282866,2	K562	blood:
17	chr8:63349340..63351905-chr8:63356599..63358880,2	K562	blood:
18	chr8:63392226..63394880-chr8:63395172..63397955,3	K562	blood:
19	chr8:63277582..63279518-chr8:63281007..63282866,2	K562	blood:
20	chr1:218393310..218393842-chr8:63404567..63405420,2	MCF-7	breast:
21	chr8:63319277..63321241-chr8:63321848..63324051,2	K562	blood:
22	chr8:63411360..63415299-chr8:63422885..63426744,3	K562	blood:
23	chr8:63378897..63381630-chr8:63394009..63396147,2	K562	blood:
24	chr8:63414123..63416933-chr8:63426622..63428263,2	MCF-7	breast:
25	chr8:63349340..63351905-chr8:63356599..63358880,2	K562	blood:
26	chr8:63295025..63297030-chr8:63298219..63300648,2	K562	blood:
27	chr8:62722647..62723219-chr8:63317559..63318273,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GGH-1	chr8:63385776-63385989	ENSG00000254050.1
2	lnc-GGH-3	chr8:63394757-63396370	NONHSAT126906
3	lnc-GGH-1	chr8:63386530-63386828	ENSG00000254050.1

No data

Variant related genes	Relation type
ENSG00000254050	TF binding region
ENSG00000253975	TF binding region
ENSG00000254050	CpG island
ENSG00000253975	CpG island
ENSG00000253975	chromatin interactions

Extended variants
information (count: 4899 )
Associated
traits (count: 99 )

Variant overlapped rSNPs/rCNVs (count:4899 , 50 per page) page: 1 2 3 4 5 6 7 ... 98

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs149689613	chr8:63276007-63276008	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs188723114	chr8:63276086-63276087	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs530069818	chr8:63276100-63276101	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs549028908	chr8:63276107-63276108	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs567586917	chr8:63276124-63276125	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs531629514	chr8:63276151-63276152	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs529273781	chr8:63276200-63276201	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs550047067	chr8:63276242-63276243	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs181096046	chr8:63276325-63276326	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs534284761	chr8:63276326-63276327	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs6472011	chr8:63276351-63276352	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs147809713	chr8:63276378-63276379	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs10593166	chr8:63276405-63276406	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs547438659	chr8:63276407-63276408	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs35027882	chr8:63276410-63276411	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs565562988	chr8:63276415-63276416	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs184684340	chr8:63276484-63276485	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs189917256	chr8:63276494-63276495	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs6987976	chr8:63276498-63276499	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs139427697	chr8:63276505-63276506	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs537343957	chr8:63276530-63276531	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs16918923	chr8:63276532-63276533	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs7006148	chr8:63276534-63276535	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs6472012	chr8:63276580-63276581	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs182488005	chr8:63276606-63276607	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs113607365	chr8:63276610-63276611	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs6472013	chr8:63276614-63276615	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs542249292	chr8:63276631-63276632	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs563670206	chr8:63276659-63276660	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs145061189	chr8:63276727-63276728	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs370280949	chr8:63276849-63276850	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs550061104	chr8:63276951-63276952	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs111731175	chr8:63276954-63276955	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs397780434	chr8:63276955-63276956	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs201118730	chr8:63276956-63276957	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs565093523	chr8:63276963-63276964	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs532319465	chr8:63277002-63277003	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs373754080	chr8:63277011-63277012	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs528392601	chr8:63277046-63277047	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs73259209	chr8:63277060-63277061	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs547425482	chr8:63277105-63277106	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs180892574	chr8:63277117-63277118	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs184888492	chr8:63277123-63277124	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs569261942	chr8:63277129-63277130	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs369393729	chr8:63277130-63277131	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs537356489	chr8:63277139-63277140	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs558790990	chr8:63277153-63277154	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs577044339	chr8:63277154-63277155	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs535248537	chr8:63277165-63277166	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs6472014	chr8:63277170-63277171	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:99)

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
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Renal cell carcinoma	21215367	CNVD

Chromatin state (count:304 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:63272400-63276000	Enhancers	Muscle Satellite Cultured Cells	--
2	chr8:63275600-63276000	Enhancers	iPS-18 Cell Line	embryonic stem cell
3	chr8:63275800-63276000	Enhancers	A549	lung
4	chr8:63275800-63276200	Enhancers	H9 Cell Line	embryonic stem cell
5	chr8:63275800-63276200	Enhancers	HUES48 Cell Line	embryonic stem cell
6	chr8:63275800-63276200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr8:63275800-63276200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
8	chr8:63276000-63276200	Weak transcription	A549	lung
9	chr8:63276000-63276800	Enhancers	HUES64 Cell Line	embryonic stem cell
10	chr8:63276000-63281800	Weak transcription	Muscle Satellite Cultured Cells	--
11	chr8:63276200-63281600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
12	chr8:63277000-63277400	Weak transcription	HUES64 Cell Line	embryonic stem cell
13	chr8:63281000-63281200	Enhancers	Fetal Intestine Large	intestine
14	chr8:63281000-63281200	Enhancers	Fetal Intestine Small	intestine
15	chr8:63281200-63282000	Weak transcription	Fetal Intestine Large	intestine
16	chr8:63281400-63282000	Weak transcription	HUES64 Cell Line	embryonic stem cell
17	chr8:63281400-63282000	Enhancers	A549	lung
18	chr8:63281400-63282200	Weak transcription	Fetal Intestine Small	intestine
19	chr8:63281400-63283600	Enhancers	Cortex derived primary cultured neurospheres	brain
20	chr8:63281600-63283800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
21	chr8:63281800-63283000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
22	chr8:63281800-63283800	Enhancers	Fetal Kidney	kidney
23	chr8:63281800-63284200	Enhancers	Muscle Satellite Cultured Cells	--
24	chr8:63282000-63282600	Flanking Active TSS	A549	lung
25	chr8:63282000-63282800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr8:63282000-63283000	Enhancers	Fetal Intestine Large	intestine
27	chr8:63282000-63283200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
28	chr8:63282000-63283600	Enhancers	Fetal Lung	lung
29	chr8:63282000-63283600	Enhancers	NH-A	brain
30	chr8:63282200-63282600	Enhancers	iPS-18 Cell Line	embryonic stem cell
31	chr8:63282200-63283000	Enhancers	HUES64 Cell Line	embryonic stem cell
32	chr8:63282200-63283000	Enhancers	Fetal Intestine Small	intestine
33	chr8:63282600-63283600	Active TSS	A549	lung
34	chr8:63282800-63284600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr8:63283000-63284400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
36	chr8:63283600-63284000	Flanking Active TSS	A549	lung
37	chr8:63283600-63286800	Weak transcription	Cortex derived primary cultured neurospheres	brain
38	chr8:63284000-63284800	Enhancers	A549	lung
39	chr8:63284400-63284600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
40	chr8:63284600-63284800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr8:63286800-63287000	Enhancers	Cortex derived primary cultured neurospheres	brain
42	chr8:63289400-63290000	Weak transcription	Cortex derived primary cultured neurospheres	brain
43	chr8:63289800-63290000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr8:63290400-63291800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr8:63290400-63292600	ZNF genes & repeats	Cortex derived primary cultured neurospheres	brain
46	chr8:63290800-63291600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
47	chr8:63291200-63291400	ZNF genes & repeats	Fetal Brain Female	brain
48	chr8:63291400-63291600	ZNF genes & repeats	Gastric	stomach
49	chr8:63292600-63307000	Weak transcription	Cortex derived primary cultured neurospheres	brain
50	chr8:63295400-63296400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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