Variant report

Variant	nsv1016883
Chromosome Location	chr8:63110741-63171354
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:446)
CpG islands
(count:1221)
Chromatin interactive
region (count:5)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:446 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:63162335-63162587	HepG2	liver:	n/a	n/a
2	BACH1	chr8:63161254-63161272	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr8:63162004-63162082	H1-hESC	embryonic stem cell:	n/a	n/a
4	BCL3	chr8:63146882-63147588	A549	lung:	n/a	n/a
5	CEBPB	chr8:63146936-63147637	A549	lung:	n/a	n/a
6	CEBPB	chr8:63162970-63163351	Hela-S3	cervix:	n/a	chr8:63163165-63163178 chr8:63163167-63163178
7	CEBPB	chr8:63162998-63163340	A549	lung:	n/a	chr8:63163165-63163178 chr8:63163167-63163178
8	CHD1	chr8:63161096-63161206	H1-hESC	embryonic stem cell:	n/a	n/a
9	CHD2	chr8:63161665-63162207	H1-hESC	embryonic stem cell:	n/a	n/a
10	CHD2	chr8:63162467-63162593	HepG2	liver:	n/a	n/a
11	CHD2	chr8:63160560-63160730	H1-hESC	embryonic stem cell:	n/a	n/a
12	CREB1	chr8:63161387-63161992	A549	lung:	n/a	n/a
13	CTBP2	chr8:63160517-63162469	H1-hESC	embryonic stem cell:	n/a	n/a
14	CTCF	chr8:63157600-63157750	GM12869	blood:	n/a	n/a
15	CTCF	chr8:63167860-63168010	HepG2	liver:	n/a	n/a
16	CTCF	chr8:63167900-63168050	HCPEpiC	choroid plexus:	n/a	n/a
17	CTCF	chr8:63160554-63160824	A549	lung:	n/a	chr8:63160696-63160705
18	CTCF	chr8:63167840-63167990	Hela-S3	cervix:	n/a	n/a
19	CTCF	chr8:63157660-63157810	HRPEpiC	eye:	n/a	n/a
20	CTCF	chr8:63157649-63157850	K562	blood:	n/a	n/a
21	CTCF	chr8:63157540-63157690	GM12870	blood:	n/a	n/a
22	CTCF	chr8:63157640-63157790	GM06990	blood:	n/a	n/a
23	CTCF	chr8:63167880-63168030	HCT-116	colon:	n/a	n/a
24	CTCF	chr8:63160560-63160710	Caco-2	colon:	n/a	chr8:63160696-63160705
25	CTCF	chr8:63160020-63160170	HBMEC	blood vessel:	n/a	n/a
26	CTCF	chr8:63160000-63160150	HBMEC	blood vessel:	n/a	n/a
27	CTCF	chr8:63157660-63157810	AG04450	lung:	n/a	n/a
28	CTCF	chr8:63157620-63157770	HPF	lung:	n/a	n/a
29	CTCF	chr8:63167800-63167950	HCT-116	colon:	n/a	n/a
30	CTCF	chr8:63167900-63168050	HPAF	blood vessel:	n/a	n/a
31	CTCF	chr8:63157620-63157770	HEK293	kidney:	n/a	n/a
32	CTCF	chr8:63167920-63168070	HEK293	kidney:	n/a	n/a
33	CTCF	chr8:63157580-63157830	GM06990	blood:	n/a	n/a
34	CTCF	chr8:63157640-63157790	GM12878	blood:	n/a	n/a
35	CTCF	chr8:63160620-63160770	GM12864	blood:	n/a	chr8:63160696-63160705
36	CTCF	chr8:63157560-63157710	HVMF	connective:	n/a	n/a
37	CTCF	chr8:63157600-63157750	NHEK	skin:	n/a	n/a
38	CTCF	chr8:63161853-63161939	MCF-7	breast:	n/a	chr8:63161885-63161898
39	CTCF	chr8:63157640-63157790	AG04450	lung:	n/a	n/a
40	CTCF	chr8:63157620-63157770	GM12864	blood:	n/a	n/a
41	CTCF	chr8:63157660-63157810	HMF	breast:	n/a	n/a
42	CTCF	chr8:63160537-63160804	H1-hESC	embryonic stem cell:	n/a	chr8:63160696-63160705
43	CTCF	chr8:63160600-63160750	HepG2	liver:	n/a	chr8:63160696-63160705
44	CTCF	chr8:63167940-63168090	MCF-7	breast:	n/a	n/a
45	CTCF	chr8:63157700-63157850	HCPEpiC	choroid plexus:	n/a	n/a
46	CTCF	chr8:63160580-63160730	AG04450	lung:	n/a	chr8:63160696-63160705
47	CTCF	chr8:63167900-63168050	HBMEC	blood vessel:	n/a	n/a
48	CTCF	chr8:63167840-63167990	NHEK	skin:	n/a	n/a
49	CTCF	chr8:63157700-63157850	Hela-S3	cervix:	n/a	n/a
50	CTCF	chr8:63157720-63157870	HRE	kidney:	n/a	n/a

(count:1221 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:63164796-63164846	PANC-1	pancreas:	n/a
2	chr8:63164796-63164846	PANC-1	pancreas:	n/a
3	chr8:63160853-63160903	MCF-7	breast:	n/a
4	chr8:63160853-63160903	ECC-1	luminal epithelium:	n/a
5	chr8:63160417-63160467	NHBE	bronchial:	n/a
6	chr8:63161676-63161726	MCF10A-Er-Src	breast:	n/a
7	chr8:63161676-63161726	Hepatocyte	liver:	n/a
8	chr8:63161676-63161726	HRCEpiC	kidney:	n/a
9	chr8:63160256-63160306	H1-hESC	embryonic stem cell:	embryo
10	chr8:63161579-63161629	A549	lung:	n/a
11	chr8:63160256-63160306	K562	blood:	n/a
12	chr8:63160853-63160903	H1-hESC	embryonic stem cell:	embryo
13	chr8:63161077-63161127	MCF-7	breast:	n/a
14	chr8:63162277-63162327	BE2_C	brain:	n/a
15	chr8:63161589-63161639	ECC-1	luminal epithelium:	n/a
16	chr8:63160256-63160306	PANC-1	pancreas:	n/a
17	chr8:63160853-63160903	GM19239	blood:	n/a
18	chr8:63164796-63164846	SAEC	small airway:	n/a
19	chr8:63158463-63158513	NB4	blood:	n/a
20	chr8:63164796-63164846	T-47D	breast:	n/a
21	chr8:63160417-63160467	AG09319	gingival:	n/a
22	chr8:63158463-63158513	BJ	skin:	n/a
23	chr8:63160417-63160467	PrEC	prostate:	n/a
24	chr8:63160853-63160903	GM12878	blood:	n/a
25	chr8:63160547-63160597	HEEpiC	esophagus:	n/a
26	chr8:63158463-63158513	HRPEpiC	eye:	n/a
27	chr8:63160417-63160467	HUVEC	blood vessel:	n/a
28	chr8:63160282-63160332	GM06990	blood:	n/a
29	chr8:63160761-63160811	GM12892	blood:	n/a
30	chr8:63161589-63161639	PFSK-1	brain:	n/a
31	chr8:63162277-63162327	HEEpiC	esophagus:	n/a
32	chr8:63161579-63161629	AG09319	gingival:	n/a
33	chr8:63162277-63162327	HL-60	blood:	n/a
34	chr8:63160256-63160306	GM19239	blood:	n/a
35	chr8:63160256-63160306	LNCaP	prostate:	n/a
36	chr8:63161589-63161639	Caco-2	colon:	n/a
37	chr8:63160547-63160597	AoSMC	blood vessel:	n/a
38	chr8:63160417-63160467	A549	lung:	n/a
39	chr8:63161676-63161726	H1-hESC	embryonic stem cell:	embryo
40	chr8:63161676-63161726	AG04449	skin:	fetal
41	chr8:63161589-63161639	SK-N-SH	brain:	n/a
42	chr8:63161589-63161639	HCPEpiC	choroid plexus:	n/a
43	chr8:63160547-63160597	HPAEpiC	pulmonary alveolar:	n/a
44	chr8:63161616-63161666	T-47D	breast:	n/a
45	chr8:63160256-63160306	SK-N-SH_RA	brain:	n/a
46	chr8:63160761-63160811	IMR90	lung:	fetal
47	chr8:63160761-63160811	SAEC	small airway:	n/a
48	chr8:63161579-63161629	PrEC	prostate:	n/a
49	chr8:63160509-63160559	BE2_C	brain:	n/a
50	chr8:63162277-63162327	T-47D	breast:	n/a

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:63163914..63166859-chr8:63167989..63170549,2	MCF-7	breast:
2	chr8:63163914..63166859-chr8:63167989..63170549,2	MCF-7	breast:
3	chr8:63153468..63155828-chr8:63369225..63371318,2	MCF-7	breast:
4	chr8:63157703..63161119-chr8:63165423..63168636,3	K562	blood:
5	chr8:63157703..63161119-chr8:63165423..63168636,3	K562	blood:

No data

Variant related genes	Relation type
NKAIN3	TF binding region
NKAIN3	CpG island

Extended variants
information (count: 1293 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:1293 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs556241675	chr8:63111403-63111404	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs148808639	chr8:63111419-63111420	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs73683010	chr8:63111421-63111422	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs369107990	chr8:63111424-63111425	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs558111322	chr8:63111426-63111427	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs573057897	chr8:63111462-63111463	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs554954646	chr8:63111463-63111464	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs118066216	chr8:63111472-63111473	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs73683011	chr8:63111495-63111496	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs568841629	chr8:63111503-63111504	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs17810421	chr8:63111513-63111514	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs73683012	chr8:63111520-63111521	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs562312707	chr8:63111608-63111609	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs554737658	chr8:63111629-63111630	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs61575867	chr8:63111630-63111631	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs551639321	chr8:63111653-63111654	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs530190229	chr8:63111658-63111659	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs181898045	chr8:63111670-63111671	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs546266868	chr8:63111705-63111706	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs150015244	chr8:63111741-63111742	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs527874145	chr8:63111759-63111760	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs373481182	chr8:63111762-63111763	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs73683013	chr8:63111763-63111764	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs376696380	chr8:63111804-63111805	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs56158875	chr8:63111881-63111882	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs187383221	chr8:63111916-63111917	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs57963179	chr8:63111924-63111925	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs145161319	chr8:63111946-63111947	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs76797073	chr8:63111973-63111974	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs546275066	chr8:63111974-63111975	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs77030719	chr8:63112027-63112028	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs117917944	chr8:63112050-63112051	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs534083849	chr8:63112070-63112071	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs569038751	chr8:63112091-63112092	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs149139293	chr8:63112105-63112106	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs75647252	chr8:63112118-63112119	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs369884870	chr8:63112129-63112130	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs536896722	chr8:63112184-63112185	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs75523950	chr8:63112201-63112202	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs80000977	chr8:63112202-63112203	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs190949825	chr8:63112204-63112205	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs113170825	chr8:63112220-63112221	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs577553915	chr8:63112225-63112226	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs73683014	chr8:63112236-63112237	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs62508761	chr8:63112237-63112238	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs573296776	chr8:63112255-63112256	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs73683015	chr8:63112259-63112260	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs542927752	chr8:63112280-63112281	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs182777124	chr8:63112298-63112299	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs531960075	chr8:63112315-63112316	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:95)

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

Chromatin state (count:524 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:63111400-63112200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr8:63111400-63112200	Enhancers	Cortex derived primary cultured neurospheres	brain
3	chr8:63111400-63112600	Enhancers	Brain Germinal Matrix	brain
4	chr8:63112600-63115000	Weak transcription	Brain Germinal Matrix	brain
5	chr8:63112800-63113600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr8:63113600-63115600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr8:63115000-63115800	Enhancers	Brain Germinal Matrix	brain
8	chr8:63115600-63116000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr8:63122800-63123000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr8:63127400-63127800	Enhancers	Primary B cells from cord blood	blood
11	chr8:63128000-63128400	Enhancers	Primary B cells from peripheral blood	blood
12	chr8:63128000-63130600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
13	chr8:63128600-63129000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
14	chr8:63128600-63130000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr8:63128800-63129200	Enhancers	A549	lung
16	chr8:63129200-63129800	Flanking Active TSS	A549	lung
17	chr8:63129200-63130400	Enhancers	NH-A	brain
18	chr8:63129400-63129800	Enhancers	HUES48 Cell Line	embryonic stem cell
19	chr8:63129400-63130600	Enhancers	HUES64 Cell Line	embryonic stem cell
20	chr8:63129600-63130200	Enhancers	Cortex derived primary cultured neurospheres	brain
21	chr8:63129600-63130400	Enhancers	HSMMtube	muscle
22	chr8:63129600-63130600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr8:63129600-63131400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr8:63129600-63131400	Enhancers	Fetal Brain Male	brain
25	chr8:63129800-63130000	Weak transcription	HUES48 Cell Line	embryonic stem cell
26	chr8:63129800-63130000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
27	chr8:63129800-63130400	Enhancers	ES-I3 Cell Line	embryonic stem cell
28	chr8:63129800-63130400	Enhancers	A549	lung
29	chr8:63130000-63130200	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
30	chr8:63130000-63130200	Enhancers	Brain Germinal Matrix	brain
31	chr8:63130000-63130200	Flanking Active TSS	Fetal Brain Female	brain
32	chr8:63130000-63130400	Enhancers	HUES48 Cell Line	embryonic stem cell
33	chr8:63130000-63130400	Active TSS	Brain Anterior Caudate	brain
34	chr8:63130200-63130400	Enhancers	Duodenum Smooth Muscle	Duodenum
35	chr8:63130200-63130400	Active TSS	Fetal Brain Female	brain
36	chr8:63130200-63130400	Enhancers	Small Intestine	intestine
37	chr8:63130200-63130400	Enhancers	GM12878-XiMat	blood
38	chr8:63130200-63130600	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
39	chr8:63130200-63130600	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
40	chr8:63130200-63130600	Flanking Active TSS	Brain Germinal Matrix	brain
41	chr8:63130200-63131800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
42	chr8:63130400-63130600	Flanking Active TSS	Fetal Brain Female	brain
43	chr8:63130600-63130800	Enhancers	Fetal Brain Female	brain
44	chr8:63130600-63131600	Weak transcription	Brain Germinal Matrix	brain
45	chr8:63130600-63131800	Enhancers	Cortex derived primary cultured neurospheres	brain
46	chr8:63130800-63131200	Weak transcription	Fetal Brain Female	brain
47	chr8:63131200-63131800	Enhancers	Fetal Brain Female	brain
48	chr8:63131600-63132400	Enhancers	Brain Germinal Matrix	brain
49	chr8:63132200-63132400	Enhancers	HUES48 Cell Line	embryonic stem cell
50	chr8:63143400-63144400	Enhancers	A549	lung

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