Variant report

Variant	nsv831339
Chromosome Location	chr8:63312449-63501127
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:499)
CpG islands
(count:244)
Chromatin interactive
region (count:25)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:499 , 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	chr8:63374900-63374966	HepG2	liver:	n/a	n/a
2	ARID3A	chr8:63435769-63436270	HepG2	liver:	n/a	n/a
3	ATF1	chr8:63421756-63421925	K562	blood:	n/a	n/a
4	BCL11A	chr8:63385596-63385878	GM12878	blood:	n/a	n/a
5	BCL3	chr8:63435720-63436281	A549	lung:	n/a	n/a
6	BHLHE40	chr8:63385606-63385742	GM12878	blood:	n/a	n/a
7	CBX3	chr8:63415983-63416273	K562	blood:	n/a	n/a
8	CCNT2	chr8:63485440-63485711	K562	blood:	n/a	n/a
9	CEBPB	chr8:63442626-63443017	A549	lung:	n/a	chr8:63442821-63442832
10	CEBPB	chr8:63418482-63418719	A549	lung:	n/a	n/a
11	CEBPB	chr8:63368097-63368297	HepG2	liver:	n/a	chr8:63368175-63368186
12	CEBPB	chr8:63436941-63437400	MCF-7	breast:	n/a	n/a
13	CEBPB	chr8:63451730-63451893	HepG2	liver:	n/a	chr8:63451861-63451872 chr8:63451832-63451843
14	CEBPB	chr8:63435813-63436186	HepG2	liver:	n/a	n/a
15	CEBPB	chr8:63442643-63442999	HepG2	liver:	n/a	chr8:63442821-63442832
16	CEBPB	chr8:63402982-63403185	HepG2	liver:	n/a	chr8:63403061-63403072
17	CEBPB	chr8:63435779-63436222	A549	lung:	n/a	n/a
18	CEBPB	chr8:63431742-63431833	A549	lung:	n/a	n/a
19	CEBPB	chr8:63442422-63443079	A549	lung:	n/a	chr8:63442821-63442832
20	CEBPB	chr8:63442336-63443120	MCF-7	breast:	n/a	chr8:63442821-63442832
21	CEBPB	chr8:63337890-63338193	HepG2	liver:	n/a	chr8:63338032-63338043
22	CEBPB	chr8:63435809-63436173	A549	lung:	n/a	n/a
23	CEBPB	chr8:63337971-63338145	A549	lung:	n/a	chr8:63338032-63338043
24	CEBPB	chr8:63442377-63443054	MCF-7	breast:	n/a	chr8:63442821-63442832
25	CEBPB	chr8:63435732-63436260	A549	lung:	n/a	n/a
26	CEBPB	chr8:63334351-63334505	HepG2	liver:	n/a	n/a
27	CEBPB	chr8:63435598-63436346	MCF-7	breast:	n/a	n/a
28	CEBPB	chr8:63455915-63456147	HepG2	liver:	n/a	chr8:63456020-63456033 chr8:63456020-63456031
29	CEBPB	chr8:63381751-63381991	HepG2	liver:	n/a	chr8:63381841-63381852
30	CEBPB	chr8:63381816-63381998	A549	lung:	n/a	chr8:63381841-63381852
31	CEBPB	chr8:63435646-63436271	MCF-7	breast:	n/a	n/a
32	CEBPB	chr8:63499743-63500029	HepG2	liver:	n/a	chr8:63499893-63499904 chr8:63499893-63499906 chr8:63499895-63499904 chr8:63499895-63499906
33	CEBPB	chr8:63464611-63464680	A549	lung:	n/a	n/a
34	CEBPB	chr8:63418397-63418745	IMR90	lung:	n/a	n/a
35	CEBPB	chr8:63469731-63469940	A549	lung:	n/a	chr8:63469817-63469828
36	CEBPB	chr8:63469738-63469903	HepG2	liver:	n/a	chr8:63469817-63469828
37	CTCF	chr8:63321767-63321844	GM10266	blood:	n/a	n/a
38	CTCF	chr8:63368997-63369049	MCF-7	breast:	n/a	n/a
39	CTCF	chr8:63317740-63317890	WERI-Rb-1	eye:	n/a	n/a
40	CTCF	chr8:63317660-63317810	GM12878	blood:	n/a	n/a
41	CTCF	chr8:63317751-63317928	Kidney_OC	kidney:	n/a	n/a
42	CTCF	chr8:63317740-63317890	GM12878	blood:	n/a	n/a
43	CTCF	chr8:63317671-63317877	HepG2	liver:	n/a	n/a
44	CTCF	chr8:63317680-63317830	HMEC	breast:	n/a	n/a
45	CTCF	chr8:63317611-63318112	MCF-7	breast:	n/a	n/a
46	CTCF	chr8:63317720-63317870	MCF-7	breast:	n/a	n/a
47	CTCF	chr8:63317760-63317910	GM12875	blood:	n/a	n/a
48	CTCF	chr8:63317720-63317919	GM19238	blood:	n/a	n/a
49	CTCF	chr8:63317820-63317970	GM12871	blood:	n/a	n/a
50	CTCF	chr8:63317720-63317870	HEEpiC	esophagus:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:63438306-63438356	SK-N-SH_RA	brain:	n/a
2	chr8:63444750-63444800	PANC-1	pancreas:	n/a
3	chr8:63385433-63385483	SK-N-SH	brain:	n/a
4	chr8:63385433-63385483	AG04449	skin:	fetal
5	chr8:63438306-63438356	ECC-1	luminal epithelium:	n/a
6	chr8:63444750-63444800	HCM	heart:	n/a
7	chr8:63444750-63444800	U87	brain:	n/a
8	chr8:63403502-63403552	PANC-1	pancreas:	n/a
9	chr8:63438306-63438356	AG04450	lung:	fetal
10	chr8:63444750-63444800	BE2_C	brain:	n/a
11	chr8:63403502-63403552	SAEC	small airway:	n/a
12	chr8:63385433-63385483	GM19239	blood:	n/a
13	chr8:63438306-63438356	Hepatocyte	liver:	n/a
14	chr8:63438306-63438356	SK-N-MC	brain:	n/a
15	chr8:63438306-63438356	Caco-2	colon:	n/a
16	chr8:63403502-63403552	NHBE	bronchial:	n/a
17	chr8:63403502-63403552	HRCEpiC	kidney:	n/a
18	chr8:63385433-63385483	SKMC	muscle:	n/a
19	chr8:63444750-63444800	AoSMC	blood vessel:	n/a
20	chr8:63438306-63438356	NHBE	bronchial:	n/a
21	chr8:63403502-63403552	GM19239	blood:	n/a
22	chr8:63444750-63444800	HAEpiC	amniotic membrane:	n/a
23	chr8:63403502-63403552	ovcar-3	ovarian:	n/a
24	chr8:63403502-63403552	AG09309	skin:	n/a
25	chr8:63438306-63438356	A549	lung:	n/a
26	chr8:63403502-63403552	Caco-2	colon:	n/a
27	chr8:63444750-63444800	SKMC	muscle:	n/a
28	chr8:63438306-63438356	RPTEC	kidney:	n/a
29	chr8:63444750-63444800	PFSK-1	brain:	n/a
30	chr8:63385433-63385483	IMR90	lung:	fetal
31	chr8:63403502-63403552	HRPEpiC	eye:	n/a
32	chr8:63385433-63385483	HCPEpiC	choroid plexus:	n/a
33	chr8:63438306-63438356	HPAEpiC	pulmonary alveolar:	n/a
34	chr8:63385433-63385483	AoSMC	blood vessel:	n/a
35	chr8:63444750-63444800	HCPEpiC	choroid plexus:	n/a
36	chr8:63438306-63438356	NB4	blood:	n/a
37	chr8:63385433-63385483	GM12891	blood:	n/a
38	chr8:63438306-63438356	U87	brain:	n/a
39	chr8:63444750-63444800	HMEC	breast:	n/a
40	chr8:63438306-63438356	AG10803	skin:	n/a
41	chr8:63385433-63385483	K562	blood:	n/a
42	chr8:63438306-63438356	PANC-1	pancreas:	n/a
43	chr8:63444750-63444800	SK-N-SH_RA	brain:	n/a
44	chr8:63438306-63438356	K562	blood:	n/a
45	chr8:63444750-63444800	HPAEpiC	pulmonary alveolar:	n/a
46	chr8:63444750-63444800	ECC-1	luminal epithelium:	n/a
47	chr8:63403502-63403552	MCF10A-Er-Src	breast:	n/a
48	chr8:63444750-63444800	CMK	blood:	n/a
49	chr8:63403502-63403552	GM12878	blood:	n/a
50	chr8:63385433-63385483	HEEpiC	esophagus:	n/a

(count:25 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:62722647..62723219-chr8:63317559..63318273,2	MCF-7	breast:
2	chr8:63444142..63446128-chr8:63448554..63450690,2	K562	blood:
3	chr8:63378897..63381630-chr8:63394009..63396147,2	K562	blood:
4	chr8:63355392..63357928-chr8:63359748..63362199,2	K562	blood:
5	chr21:46294976..46295889-chr8:63408636..63409252,2	MCF-7	breast:
6	chr8:63414123..63416933-chr8:63426622..63428263,2	MCF-7	breast:
7	chr8:63318987..63320777-chr8:63321010..63323348,2	K562	blood:
8	chr8:63319277..63321241-chr8:63321848..63324051,2	K562	blood:
9	chr8:63052210..63052840-chr8:63317439..63317973,2	MCF-7	breast:
10	chr1:218393310..218393842-chr8:63404567..63405420,2	MCF-7	breast:
11	chr8:63444142..63446128-chr8:63448554..63450690,2	K562	blood:
12	chr8:63349340..63351905-chr8:63356599..63358880,2	K562	blood:
13	chr8:63355392..63357928-chr8:63359748..63362199,2	K562	blood:
14	chr8:63411360..63415299-chr8:63422885..63426744,3	K562	blood:
15	chr8:63153468..63155828-chr8:63369225..63371318,2	MCF-7	breast:
16	chr8:63378897..63381630-chr8:63394009..63396147,2	K562	blood:
17	chr8:63043534..63044140-chr8:63317610..63318142,2	MCF-7	breast:
18	chr8:63349340..63351905-chr8:63356599..63358880,2	K562	blood:
19	chr8:63319277..63321241-chr8:63321848..63324051,2	K562	blood:
20	chr8:63414123..63416933-chr8:63426622..63428263,2	MCF-7	breast:
21	chr8:63460557..63464454-chr8:63467643..63469936,3	MCF-7	breast:
22	chr8:63411360..63415299-chr8:63422885..63426744,3	K562	blood:
23	chr8:63318987..63320777-chr8:63321010..63323348,2	K562	blood:
24	chr8:63460557..63464454-chr8:63467643..63469936,3	MCF-7	breast:
25	chr8:63392226..63394880-chr8:63395172..63397955,3	K562	blood:

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

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

No data

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

Extended variants
information (count: 4910 )
Associated
traits (count: 100 )

Variant overlapped rSNPs/rCNVs (count:4910 , 50 per page) page: 1 2 3 4 5 6 7 ... 99

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs527927176	chr8:63312491-63312492	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs549156664	chr8:63312501-63312502	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs372602806	chr8:63312530-63312531	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs192939056	chr8:63312562-63312563	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs376011411	chr8:63312565-63312566	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs563182314	chr8:63312588-63312589	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs563080833	chr8:63312613-63312614	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs377245224	chr8:63312625-63312626	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs374095739	chr8:63312639-63312640	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs370118542	chr8:63312681-63312682	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs556352319	chr8:63312689-63312690	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs571629965	chr8:63312701-63312702	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs538613173	chr8:63312722-63312723	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs558084596	chr8:63312727-63312728	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs573168986	chr8:63312728-63312729	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs576542335	chr8:63312729-63312730	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs79999968	chr8:63312740-63312741	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs71255333	chr8:63312742-63312743	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs374354358	chr8:63312753-63312754	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs573728438	chr8:63312755-63312756	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs185086037	chr8:63312828-63312829	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs190560404	chr8:63312849-63312850	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs542174277	chr8:63312850-63312851	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs559128415	chr8:63312858-63312859	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs376871059	chr8:63312860-63312861	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs544676298	chr8:63312875-63312876	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs62509245	chr8:63312884-63312885	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs527962800	chr8:63312890-63312891	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs549191778	chr8:63312891-63312892	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs182349096	chr8:63312915-63312916	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs376354218	chr8:63312919-63312920	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs550254588	chr8:63312960-63312961	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs527958112	chr8:63312982-63312983	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs149992220	chr8:63312983-63312984	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs547800024	chr8:63313027-63313028	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs10091479	chr8:63313049-63313050	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs368239157	chr8:63313053-63313054	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs555667363	chr8:63313063-63313064	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs573790587	chr8:63313090-63313091	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs185199079	chr8:63313094-63313095	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs556271892	chr8:63313115-63313116	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs547422246	chr8:63313120-63313121	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs188061623	chr8:63313158-63313159	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs564129215	chr8:63313193-63313194	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs546168486	chr8:63313260-63313261	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs5891853	chr8:63313261-63313262	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs372719348	chr8:63313271-63313272	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs77806181	chr8:63313272-63313273	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs544639070	chr8:63313281-63313282	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs74878640	chr8:63313287-63313288	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:100)

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
Schizophrenia	23813976	CNVD

Chromatin state (count:363 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:63308000-63314000	Weak transcription	Cortex derived primary cultured neurospheres	brain
2	chr8:63311800-63313200	Enhancers	Muscle Satellite Cultured Cells	--
3	chr8:63312200-63312600	Enhancers	NH-A	brain
4	chr8:63312600-63314200	Weak transcription	NH-A	brain
5	chr8:63313200-63314400	Weak transcription	Muscle Satellite Cultured Cells	--
6	chr8:63314000-63316400	ZNF genes & repeats	Cortex derived primary cultured neurospheres	brain
7	chr8:63314200-63314600	Enhancers	NH-A	brain
8	chr8:63314400-63314800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr8:63314400-63315200	Enhancers	Muscle Satellite Cultured Cells	--
10	chr8:63314600-63316800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr8:63315000-63315400	Weak transcription	H1 Cell Line	embryonic stem cell
12	chr8:63315200-63321200	Weak transcription	Muscle Satellite Cultured Cells	--
13	chr8:63316000-63316200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr8:63316000-63316600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
15	chr8:63316000-63316600	ZNF genes & repeats	Fetal Brain Female	brain
16	chr8:63316400-63317600	Strong transcription	Cortex derived primary cultured neurospheres	brain
17	chr8:63316600-63317800	Strong transcription	Fetal Brain Female	brain
18	chr8:63316600-63318200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
19	chr8:63317000-63317600	Enhancers	H1 Cell Line	embryonic stem cell
20	chr8:63317400-63317800	Enhancers	H9 Cell Line	embryonic stem cell
21	chr8:63317600-63333000	Weak transcription	Cortex derived primary cultured neurospheres	brain
22	chr8:63317800-63318000	Weak transcription	Fetal Brain Female	brain
23	chr8:63318200-63318400	Weak transcription	Fetal Brain Female	brain
24	chr8:63321200-63321600	Enhancers	Muscle Satellite Cultured Cells	--
25	chr8:63327600-63330600	Weak transcription	Fetal Brain Male	brain
26	chr8:63333600-63334200	Enhancers	HSMM	muscle
27	chr8:63333600-63335000	Enhancers	Muscle Satellite Cultured Cells	--
28	chr8:63333800-63336000	Enhancers	HMEC	breast
29	chr8:63334200-63335400	Weak transcription	HSMM	muscle
30	chr8:63334400-63335800	Enhancers	NH-A	brain
31	chr8:63335000-63335800	Flanking Active TSS	Muscle Satellite Cultured Cells	--
32	chr8:63335400-63336000	Enhancers	HSMM	muscle
33	chr8:63335800-63336600	Weak transcription	NH-A	brain
34	chr8:63335800-63337000	Enhancers	Muscle Satellite Cultured Cells	--
35	chr8:63336000-63336600	Weak transcription	HMEC	breast
36	chr8:63336000-63336600	Weak transcription	HSMM	muscle
37	chr8:63336600-63336800	Enhancers	HMEC	breast
38	chr8:63336600-63336800	Enhancers	HSMM	muscle
39	chr8:63336600-63336800	Enhancers	NH-A	brain
40	chr8:63341600-63342400	Enhancers	Sigmoid Colon	Sigmoid Colon
41	chr8:63342200-63342800	Enhancers	Rectal Mucosa Donor 31	rectum
42	chr8:63346400-63348400	Enhancers	Muscle Satellite Cultured Cells	--
43	chr8:63346600-63346800	Bivalent Enhancer	Aorta	Aorta
44	chr8:63346600-63348200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
45	chr8:63346600-63348600	Enhancers	NH-A	brain
46	chr8:63347400-63349000	Enhancers	HSMM	muscle
47	chr8:63347600-63348200	Enhancers	HMEC	breast
48	chr8:63347600-63348800	Enhancers	Fetal Kidney	kidney
49	chr8:63347800-63348200	Enhancers	HSMMtube	muscle
50	chr8:63348800-63352200	Weak transcription	Fetal Kidney	kidney

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