Variant report

Variant	nsv890971
Chromosome Location	chr8:65028814-65242166
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:552)
CpG islands
(count:61)
Chromatin interactive
region (count:20)
LncRNA
region (count:11)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:552 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr8:65042238-65042371	K562	blood:	n/a	n/a
2	ATF1	chr8:65170426-65170525	K562	blood:	n/a	n/a
3	ATF2	chr8:65208321-65208768	GM12878	blood:	n/a	n/a
4	BACH1	chr8:65070219-65070378	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr8:65085756-65085848	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr8:65176538-65177054	H1-hESC	embryonic stem cell:	n/a	n/a
7	BATF	chr8:65121700-65121971	GM12878	blood:	n/a	n/a
8	BATF	chr8:65208366-65208711	GM12878	blood:	n/a	n/a
9	BATF	chr8:65208360-65208761	GM12878	blood:	n/a	n/a
10	BCL11A	chr8:65070199-65070390	H1-hESC	embryonic stem cell:	n/a	n/a
11	BCL11A	chr8:65070116-65070347	H1-hESC	embryonic stem cell:	n/a	n/a
12	BCL3	chr8:65066496-65066770	GM12878	blood:	n/a	n/a
13	BRCA1	chr8:65150214-65150290	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr8:65150037-65150319	HepG2	liver:	n/a	chr8:65150157-65150168
15	CEBPB	chr8:65182832-65183177	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr8:65069982-65070448	H1-hESC	embryonic stem cell:	n/a	n/a
17	CEBPB	chr8:65066130-65066170	H1-hESC	embryonic stem cell:	n/a	chr8:65066141-65066152
18	CEBPB	chr8:65085897-65086121	A549	lung:	n/a	n/a
19	CEBPB	chr8:65066000-65066302	IMR90	lung:	n/a	chr8:65066141-65066152 chr8:65066046-65066057
20	CEBPB	chr8:65195197-65195290	A549	lung:	n/a	chr8:65195249-65195260
21	CEBPB	chr8:65150065-65150345	Hela-S3	cervix:	n/a	chr8:65150157-65150168
22	CEBPB	chr8:65150096-65150324	A549	lung:	n/a	chr8:65150157-65150168
23	CEBPB	chr8:65065357-65065562	HepG2	liver:	n/a	chr8:65065418-65065429
24	CEBPB	chr8:65049677-65049944	HepG2	liver:	n/a	chr8:65049824-65049841 chr8:65049826-65049837
25	CEBPB	chr8:65060843-65061075	A549	lung:	n/a	chr8:65060937-65060948
26	CEBPB	chr8:65066032-65066276	A549	lung:	n/a	chr8:65066141-65066152 chr8:65066046-65066057
27	CEBPB	chr8:65192014-65192299	HepG2	liver:	n/a	chr8:65192136-65192145 chr8:65192134-65192145 chr8:65192134-65192147 chr8:65192136-65192147
28	CEBPB	chr8:65089913-65090024	HepG2	liver:	n/a	chr8:65089920-65089931
29	CEBPB	chr8:65065988-65066305	HepG2	liver:	n/a	chr8:65066141-65066152 chr8:65066046-65066057
30	CEBPB	chr8:65060811-65061097	HepG2	liver:	n/a	chr8:65060937-65060948
31	CEBPB	chr8:65152554-65152659	HepG2	liver:	n/a	n/a
32	CEBPB	chr8:65195182-65195388	HepG2	liver:	n/a	chr8:65195249-65195260
33	CTCF	chr8:65196340-65196490	GM12872	blood:	n/a	chr8:65196433-65196446
34	CTCF	chr8:65176820-65176970	Hela-S3	cervix:	n/a	n/a
35	CTCF	chr8:65176841-65177042	HepG2	liver:	n/a	n/a
36	CTCF	chr8:65176826-65176995	GM12892	blood:	n/a	n/a
37	CTCF	chr8:65196380-65196530	RPTEC	kidney:	n/a	chr8:65196433-65196446
38	CTCF	chr8:65196320-65196470	HRE	kidney:	n/a	chr8:65196433-65196446
39	CTCF	chr8:65196400-65196550	GM12870	blood:	n/a	chr8:65196433-65196446
40	CTCF	chr8:65196280-65196430	GM12872	blood:	n/a	n/a
41	CTCF	chr8:65196417-65196468	GM10266	blood:	n/a	chr8:65196433-65196446
42	CTCF	chr8:65176900-65177050	HRE	kidney:	n/a	n/a
43	CTCF	chr8:65196340-65196490	GM12864	blood:	n/a	chr8:65196433-65196446
44	CTCF	chr8:65196380-65196484	GM19240	blood:	n/a	chr8:65196433-65196446
45	CTCF	chr8:65196266-65196538	MCF-7	breast:	n/a	chr8:65196433-65196446
46	CTCF	chr8:65176880-65177030	HepG2	liver:	n/a	n/a
47	CTCF	chr8:65176900-65177050	GM12866	blood:	n/a	n/a
48	CTCF	chr8:65111520-65111670	MCF-7	breast:	n/a	n/a
49	CTCF	chr8:65176821-65177087	A549	lung:	n/a	n/a
50	CTCF	chr8:65176680-65176830	GM12878	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:65152945-65152995	CMK	blood:	n/a
2	chr8:65152945-65152995	IMR90	lung:	fetal
3	chr8:65152945-65152995	MCF-7	breast:	n/a
4	chr8:65152945-65152995	HL-60	blood:	n/a
5	chr8:65152945-65152995	LNCaP	prostate:	n/a
6	chr8:65152945-65152995	Caco-2	colon:	n/a
7	chr8:65152945-65152995	A549	lung:	n/a
8	chr8:65152945-65152995	HCM	heart:	n/a
9	chr8:65152945-65152995	ECC-1	luminal epithelium:	n/a
10	chr8:65152945-65152995	HAEpiC	amniotic membrane:	n/a
11	chr8:65152945-65152995	SK-N-SH	brain:	n/a
12	chr8:65152945-65152995	HRPEpiC	eye:	n/a
13	chr8:65152945-65152995	PANC-1	pancreas:	n/a
14	chr8:65152945-65152995	RPTEC	kidney:	n/a
15	chr8:65152945-65152995	SKMC	muscle:	n/a
16	chr8:65152945-65152995	HEEpiC	esophagus:	n/a
17	chr8:65152945-65152995	SAEC	small airway:	n/a
18	chr8:65152945-65152995	BE2_C	brain:	n/a
19	chr8:65152945-65152995	Hela-S3	cervix:	n/a
20	chr8:65152945-65152995	HEK293	kidney:	embryo
21	chr8:65152945-65152995	GM12878	blood:	n/a
22	chr8:65152945-65152995	HRCEpiC	kidney:	n/a
23	chr8:65152945-65152995	NHDF-neo	bronchial:	n/a
24	chr8:65152945-65152995	ProgFib	skin:	n/a
25	chr8:65152945-65152995	ovcar-3	ovarian:	n/a
26	chr8:65152945-65152995	PrEC	prostate:	n/a
27	chr8:65152945-65152995	HUVEC	blood vessel:	n/a
28	chr8:65152945-65152995	Hepatocyte	liver:	n/a
29	chr8:65152945-65152995	Jurkat	blood:	n/a
30	chr8:65152945-65152995	U87	brain:	n/a
31	chr8:65152945-65152995	AoSMC	blood vessel:	n/a
32	chr8:65152945-65152995	HNPCEpiC	eye:	n/a
33	chr8:65152945-65152995	MCF10A-Er-Src	breast:	n/a
34	chr8:65152945-65152995	HMEC	breast:	n/a
35	chr8:65152945-65152995	AG04449	skin:	fetal
36	chr8:65152945-65152995	AG09319	gingival:	n/a
37	chr8:65152945-65152995	T-47D	breast:	n/a
38	chr8:65152945-65152995	K562	blood:	n/a
39	chr8:65152945-65152995	AG09309	skin:	n/a
40	chr8:65152945-65152995	HRE	kidney:	n/a
41	chr8:65152945-65152995	AG04450	lung:	fetal
42	chr8:65152945-65152995	HCF	heart:	n/a
43	chr8:65152945-65152995	NHBE	bronchial:	n/a
44	chr8:65152945-65152995	HCT-116	colon:	n/a
45	chr8:65152945-65152995	NB4	blood:	n/a
46	chr8:65152945-65152995	PFSK-1	brain:	n/a
47	chr8:65152945-65152995	BJ	skin:	n/a
48	chr8:65152945-65152995	H1-hESC	embryonic stem cell:	embryo
49	chr8:65152945-65152995	GM06990	blood:	n/a
50	chr8:65152945-65152995	SK-N-SH_RA	brain:	n/a

(count:20 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:65121358..65123984-chr8:65128022..65129951,3	K562	blood:
2	chr8:65061835..65063681-chr8:65066858..65068581,2	MCF-7	breast:
3	chr8:65166067..65168233-chr8:65170206..65171812,2	MCF-7	breast:
4	chr8:65125718..65128574-chr8:65129073..65131314,2	K562	blood:
5	chr8:65121358..65123984-chr8:65128022..65129951,3	K562	blood:
6	chr8:65125718..65128574-chr8:65129073..65131314,2	K562	blood:
7	chr20:45282955..45284476-chr8:65144448..65146443,2	MCF-7	breast:
8	chr8:64539103..64540764-chr8:65177326..65179205,2	MCF-7	breast:
9	chr8:65166067..65168233-chr8:65170206..65171812,2	MCF-7	breast:
10	chr8:65168552..65171425-chr8:65171785..65174235,2	K562	blood:
11	chr8:64514718..64515954-chr8:65176080..65177460,13	MCF-7	breast:
12	chr8:64662235..64663084-chr8:65176753..65177365,3	MCF-7	breast:
13	chr8:65168552..65171425-chr8:65171785..65174235,2	K562	blood:
14	chr8:65103952..65105975-chr8:65106420..65108352,2	MCF-7	breast:
15	chr8:64540100..64540605-chr8:65176512..65177253,2	MCF-7	breast:
16	chr8:65103952..65105975-chr8:65106420..65108352,2	MCF-7	breast:
17	chr8:65061835..65063681-chr8:65066858..65068581,2	MCF-7	breast:
18	chr8:64331004..64331558-chr8:65176085..65177270,3	MCF-7	breast:
19	chr8:64662682..64663203-chr8:65176721..65177303,2	MCF-7	breast:
20	chr8:64303514..64304353-chr8:65176496..65177185,3	MCF-7	breast:

(count:11 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-32K4.2.1-4	chr8:65095917-65096061	NONHSAT126954
2	lnc-CYP7B1-6	chr8:65046005-65046071	ENSG00000253554.1
3	lnc-CYP7B1-6	chr8:65143113-65143173	ENSG00000253554.1
4	lnc-CYP7B1-6	chr8:65152997-65153063	ENSG00000253554.1
5	lnc-CYP7B1-6	chr8:65063650-65063721	ENSG00000253554.1
6	lnc-CYP7B1-6	chr8:65143113-65143176	ENSG00000253554.1
7	lnc-CYP7B1-6	chr8:65063650-65063721	ENSG00000253554.1
8	lnc-CYP7B1-6	chr8:65046005-65046071	ENSG00000253554.1
9	lnc-RP11-32K4.2.1-4	chr8:65095220-65095368	NONHSAT126954
10	lnc-CYP7B1-6	chr8:65079532-65079584	ENSG00000253554.1
11	lnc-CYP7B1-6	chr8:65046005-65046071	ENSG00000253554.1

No data

Variant related genes	Relation type
COX6CP8	TF binding region
ENSG00000253554	TF binding region
COX6CP8	CpG island
ENSG00000253554	CpG island

Extended variants
information (count: 7226 )
Associated
traits (count: 96 )

Variant overlapped rSNPs/rCNVs (count:7226 , 50 per page) page: 1 2 3 4 5 6 7 ... 145

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2166124	chr8:65028814-65028815	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs62519732	chr8:65028821-65028822	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs562804770	chr8:65028835-65028836	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs533357447	chr8:65028921-65028922	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs551512622	chr8:65028927-65028928	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs207469291	chr8:65029003-65029004	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs150162768	chr8:65029023-65029024	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs117207326	chr8:65029028-65029029	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs548991883	chr8:65029108-65029109	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs567172714	chr8:65029149-65029150	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs531609247	chr8:65029189-65029190	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs138663213	chr8:65029252-65029253	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs370373605	chr8:65029259-65029260	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs541791052	chr8:65029267-65029268	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs556196716	chr8:65029299-65029300	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs571522856	chr8:65029349-65029350	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs76806943	chr8:65029386-65029387	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs561532855	chr8:65029421-65029422	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs538883939	chr8:65029429-65029430	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs527529383	chr8:65029461-65029462	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs540717212	chr8:65029488-65029489	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs554001725	chr8:65029502-65029503	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs189705018	chr8:65029503-65029504	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs547042337	chr8:65029567-65029568	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs570220843	chr8:65029569-65029570	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs532755922	chr8:65029570-65029571	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs560561048	chr8:65029611-65029612	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs555800270	chr8:65029666-65029667	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs373382384	chr8:65029667-65029668	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs76086096	chr8:65029670-65029671	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs74475727	chr8:65029694-65029695	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs533441148	chr8:65029697-65029698	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs545236471	chr8:65029745-65029746	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs560293364	chr8:65029749-65029750	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs565083812	chr8:65029805-65029806	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs532158064	chr8:65029807-65029808	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs527860187	chr8:65029826-65029827	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs549730110	chr8:65029843-65029844	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs112140873	chr8:65029860-65029861	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs548820690	chr8:65029861-65029862	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs567313863	chr8:65029862-65029863	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs181222505	chr8:65029870-65029871	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs569585224	chr8:65029899-65029900	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs146254689	chr8:65029919-65029920	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs373981505	chr8:65029921-65029922	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs538921573	chr8:65029925-65029926	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs186661783	chr8:65029931-65029932	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs565902329	chr8:65030055-65030056	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs536410864	chr8:65030081-65030082	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs138032023	chr8:65030141-65030142	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:96)

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
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:255 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:65028600-65038400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
2	chr8:65034000-65035200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr8:65035200-65036400	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr8:65038400-65039400	ZNF genes & repeats	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
5	chr8:65038400-65040400	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr8:65039400-65049200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
7	chr8:65040400-65044200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr8:65040600-65047600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr8:65044200-65046800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr8:65046800-65059600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr8:65049200-65049400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr8:65059600-65060800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr8:65060200-65060400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr8:65060400-65060600	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr8:65060600-65070200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr8:65060800-65074000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr8:65063200-65063400	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
18	chr8:65063200-65063600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
19	chr8:65063400-65063600	Flanking Bivalent TSS/Enh	Breast Myoepithelial Primary Cells	Breast
20	chr8:65063600-65069600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
21	chr8:65064200-65064600	Enhancers	Fetal Brain Male	brain
22	chr8:65069400-65070000	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
23	chr8:65069600-65069800	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
24	chr8:65069600-65069800	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
25	chr8:65069600-65070000	Bivalent Enhancer	H9 Cell Line	embryonic stem cell
26	chr8:65069600-65070000	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
27	chr8:65069600-65071800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
28	chr8:65069600-65072000	Enhancers	iPS-20b Cell Line	embryonic stem cell
29	chr8:65069800-65070000	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
30	chr8:65069800-65070200	Enhancers	Brain Germinal Matrix	brain
31	chr8:65069800-65071800	Enhancers	HUES64 Cell Line	embryonic stem cell
32	chr8:65069800-65071800	Enhancers	iPS-15b Cell Line	embryonic stem cell
33	chr8:65069800-65072200	Enhancers	iPS-18 Cell Line	embryonic stem cell
34	chr8:65070000-65071000	Enhancers	HUES48 Cell Line	embryonic stem cell
35	chr8:65070000-65071800	Enhancers	HUES6 Cell Line	embryonic stem cell
36	chr8:65070000-65072000	Weak transcription	H1 Cell Line	embryonic stem cell
37	chr8:65070200-65070400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr8:65071000-65071600	Weak transcription	HUES48 Cell Line	embryonic stem cell
39	chr8:65071600-65071800	Enhancers	HUES48 Cell Line	embryonic stem cell
40	chr8:65071800-65072000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
41	chr8:65071800-65073600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
42	chr8:65072000-65073000	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
43	chr8:65072800-65073000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
44	chr8:65073000-65077400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
45	chr8:65073400-65075000	Enhancers	HUES48 Cell Line	embryonic stem cell
46	chr8:65073400-65075000	Enhancers	iPS-20b Cell Line	embryonic stem cell
47	chr8:65073600-65075000	Enhancers	iPS-18 Cell Line	embryonic stem cell
48	chr8:65073600-65075200	Enhancers	iPS-15b Cell Line	embryonic stem cell
49	chr8:65073800-65075400	Enhancers	HUES64 Cell Line	embryonic stem cell
50	chr8:65074000-65074600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived

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