Variant report

Variant	esv3693375
Chromosome Location	chr8:34631970-34780509
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:561)
CpG islands
(count:62)
Chromatin interactive
region (count:5)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:561 , 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	chr8:34635478-34635568	K562	blood:	n/a	n/a
2	BACH1	chr8:34715774-34716110	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr8:34682092-34682115	H1-hESC	embryonic stem cell:	n/a	n/a
4	BATF	chr8:34666435-34666675	GM12878	blood:	n/a	chr8:34666588-34666599
5	BHLHE40	chr8:34748830-34748972	K562	blood:	n/a	n/a
6	CBX3	chr8:34768143-34768474	K562	blood:	n/a	n/a
7	CEBPB	chr8:34764468-34764980	H1-hESC	embryonic stem cell:	n/a	n/a
8	CEBPB	chr8:34780336-34780752	A549	lung:	n/a	chr8:34780428-34780439
9	CEBPB	chr8:34780383-34780577	H1-hESC	embryonic stem cell:	n/a	chr8:34780428-34780439
10	CEBPB	chr8:34633426-34633445	H1-hESC	embryonic stem cell:	n/a	n/a
11	CEBPB	chr8:34762130-34762337	A549	lung:	n/a	chr8:34762171-34762182
12	CEBPB	chr8:34770836-34771056	HepG2	liver:	n/a	chr8:34770948-34770959 chr8:34770950-34770961
13	CEBPB	chr8:34681957-34682199	A549	lung:	n/a	n/a
14	CEBPB	chr8:34720392-34720686	HepG2	liver:	n/a	chr8:34720521-34720532
15	CEBPB	chr8:34696697-34696787	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr8:34714748-34715015	HepG2	liver:	n/a	chr8:34714892-34714909
17	CEBPB	chr8:34681739-34682175	HepG2	liver:	n/a	n/a
18	CEBPB	chr8:34714741-34715061	A549	lung:	n/a	chr8:34714892-34714909
19	CEBPB	chr8:34780303-34780623	HepG2	liver:	n/a	chr8:34780428-34780439
20	CEBPB	chr8:34762102-34762291	HepG2	liver:	n/a	chr8:34762171-34762182
21	CEBPB	chr8:34714672-34715084	Hela-S3	cervix:	n/a	chr8:34714892-34714909
22	CEBPB	chr8:34714587-34715103	A549	lung:	n/a	chr8:34714892-34714909
23	CEBPB	chr8:34704302-34704716	H1-hESC	embryonic stem cell:	n/a	n/a
24	CEBPB	chr8:34748728-34748963	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPB	chr8:34638946-34639265	Hela-S3	cervix:	n/a	n/a
26	CTBP2	chr8:34764394-34765081	H1-hESC	embryonic stem cell:	n/a	n/a
27	CTCF	chr8:34748880-34749030	GM12874	blood:	n/a	n/a
28	CTCF	chr8:34748840-34748990	K562	blood:	n/a	n/a
29	CTCF	chr8:34748857-34748938	GM13976	blood:	n/a	n/a
30	CTCF	chr8:34677280-34677430	HRE	kidney:	n/a	n/a
31	CTCF	chr8:34748840-34748990	HEEpiC	esophagus:	n/a	n/a
32	CTCF	chr8:34748880-34749030	HCPEpiC	choroid plexus:	n/a	n/a
33	CTCF	chr8:34748900-34749050	NB4	blood:	n/a	n/a
34	CTCF	chr8:34748860-34749010	A549	lung:	n/a	n/a
35	CTCF	chr8:34748880-34749030	RPTEC	kidney:	n/a	n/a
36	CTCF	chr8:34748713-34749113	HepG2	liver:	n/a	n/a
37	CTCF	chr8:34748743-34749040	Gliobla	brain:	n/a	n/a
38	CTCF	chr8:34748813-34748958	Fibrobl	skin:	n/a	n/a
39	CTCF	chr8:34737980-34738130	GM12869	blood:	n/a	n/a
40	CTCF	chr8:34748860-34749010	GM12873	blood:	n/a	n/a
41	CTCF	chr8:34748860-34749010	HMF	breast:	n/a	n/a
42	CTCF	chr8:34677211-34677454	H1-hESC	embryonic stem cell:	n/a	n/a
43	CTCF	chr8:34677297-34677395	H1-hESC	embryonic stem cell:	n/a	n/a
44	CTCF	chr8:34748700-34748850	HCM	heart:	n/a	n/a
45	CTCF	chr8:34748731-34748970	A549	lung:	n/a	n/a
46	CTCF	chr8:34748700-34748850	HAc	cerebellar:	n/a	n/a
47	CTCF	chr8:34748780-34748930	Caco-2	colon:	n/a	n/a
48	CTCF	chr8:34748820-34748970	BE2_C	brain:	n/a	n/a
49	CTCF	chr8:34748821-34748951	GM10248	blood:	n/a	n/a
50	CTCF	chr8:34748820-34748970	HUVEC	blood vessel:	n/a	n/a

(count:62 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:34764927-34764977	HAEpiC	amniotic membrane:	n/a
2	chr8:34764927-34764977	HAEpiC	amniotic membrane:	n/a
3	chr8:34764927-34764977	HEEpiC	esophagus:	n/a
4	chr8:34764927-34764977	HCF	heart:	n/a
5	chr8:34764927-34764977	GM12878	blood:	n/a
6	chr8:34764927-34764977	HCM	heart:	n/a
7	chr8:34764927-34764977	GM06990	blood:	n/a
8	chr8:34764927-34764977	NHDF-neo	bronchial:	n/a
9	chr8:34764927-34764977	RPTEC	kidney:	n/a
10	chr8:34764927-34764977	GM12891	blood:	n/a
11	chr8:34764927-34764977	HRE	kidney:	n/a
12	chr8:34764927-34764977	PFSK-1	brain:	n/a
13	chr8:34764927-34764977	MCF10A-Er-Src	breast:	n/a
14	chr8:34764927-34764977	Caco-2	colon:	n/a
15	chr8:34764927-34764977	NB4	blood:	n/a
16	chr8:34764927-34764977	HepG2	liver:	n/a
17	chr8:34764927-34764977	HCT-116	colon:	n/a
18	chr8:34764927-34764977	HCPEpiC	choroid plexus:	n/a
19	chr8:34764927-34764977	LNCaP	prostate:	n/a
20	chr8:34764927-34764977	K562	blood:	n/a
21	chr8:34764927-34764977	SKMC	muscle:	n/a
22	chr8:34764927-34764977	IMR90	lung:	fetal
23	chr8:34764927-34764977	Hela-S3	cervix:	n/a
24	chr8:34764927-34764977	BE2_C	brain:	n/a
25	chr8:34764927-34764977	Jurkat	blood:	n/a
26	chr8:34764927-34764977	NH-A	brain:	n/a
27	chr8:34764927-34764977	MCF-7	breast:	n/a
28	chr8:34764927-34764977	Hepatocyte	liver:	n/a
29	chr8:34764927-34764977	HIPEpiC	eye:	n/a
30	chr8:34764927-34764977	ovcar-3	ovarian:	n/a
31	chr8:34764927-34764977	GM12892	blood:	n/a
32	chr8:34764927-34764977	HRPEpiC	eye:	n/a
33	chr8:34764927-34764977	U87	brain:	n/a
34	chr8:34764927-34764977	ECC-1	luminal epithelium:	n/a
35	chr8:34764927-34764977	AG09319	gingival:	n/a
36	chr8:34764927-34764977	HL-60	blood:	n/a
37	chr8:34764927-34764977	AG04450	lung:	fetal
38	chr8:34764927-34764977	HRCEpiC	kidney:	n/a
39	chr8:34764927-34764977	BJ	skin:	n/a
40	chr8:34764927-34764977	HMEC	breast:	n/a
41	chr8:34764927-34764977	HPAEpiC	pulmonary alveolar:	n/a
42	chr8:34764927-34764977	SK-N-MC	brain:	n/a
43	chr8:34764927-34764977	T-47D	breast:	n/a
44	chr8:34764927-34764977	ProgFib	skin:	n/a
45	chr8:34764927-34764977	NHBE	bronchial:	n/a
46	chr8:34764927-34764977	SK-N-SH	brain:	n/a
47	chr8:34764927-34764977	CMK	blood:	n/a
48	chr8:34764927-34764977	AG10803	skin:	n/a
49	chr8:34764927-34764977	GM19239	blood:	n/a
50	chr8:34764927-34764977	H1-hESC	embryonic stem cell:	embryo

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

No.	Distal block	Cell Line	Cell type
1	chr8:34703366..34705867-chr8:34708071..34710392,2	K562	blood:
2	chr8:33538907..33539672-chr8:34748466..34749335,3	MCF-7	breast:
3	chr8:34703366..34705867-chr8:34708071..34710392,2	K562	blood:
4	chr8:34631157..34633123-chr8:34636753..34638642,2	K562	blood:
5	chr8:34631157..34633123-chr8:34636753..34638642,2	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-UNC5D-3	chr8:34650276-34650462	XLOC_006770
2	lnc-UNC5D-3	chr8:34650275-34650462	NONHSAT125996
3	lnc-UNC5D-3	chr8:34642570-34642589	XLOC_006770
4	lnc-UNC5D-3	chr8:34642569-34642589	NONHSAT125996

No data

Variant related genes	Relation type
ENSG00000254344	TF binding region
ENSG00000243181	TF binding region
ENSG00000254344	CpG island
ENSG00000243181	CpG island

Extended variants
information (count: 4391 )
Associated
traits (count: 118 )

Variant overlapped rSNPs/rCNVs (count:4391 , 50 per page) page: 1 2 3 4 5 6 7 ... 88

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs59074814	chr8:34634604-34634605	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs186435208	chr8:34634609-34634610	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs527433203	chr8:34634625-34634626	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs139773460	chr8:34634643-34634644	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs560384511	chr8:34634646-34634647	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs574429330	chr8:34634676-34634677	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs527532405	chr8:34634712-34634713	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs549222916	chr8:34634713-34634714	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs111587459	chr8:34634718-34634719	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs560847828	chr8:34634739-34634740	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs145283049	chr8:34634775-34634776	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs150988510	chr8:34634789-34634790	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs571562246	chr8:34634822-34634823	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs191295600	chr8:34634862-34634863	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs547723775	chr8:34634887-34634888	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs566245866	chr8:34634902-34634903	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs536470960	chr8:34634931-34634932	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs555016846	chr8:34634956-34634957	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs576478527	chr8:34635052-34635053	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs148163773	chr8:34635053-34635054	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs111410664	chr8:34635054-34635055	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs138528270	chr8:34635055-34635056	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs181475305	chr8:34635057-34635058	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs35275158	chr8:34635064-34635065	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs3034337	chr8:34635065-34635066	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs558996877	chr8:34635178-34635179	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs577361242	chr8:34635180-34635181	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs35742375	chr8:34635181-34635182	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs567719784	chr8:34635198-34635199	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs6468287	chr8:34635222-34635223	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs572184475	chr8:34635256-34635257	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs528355582	chr8:34635311-34635312	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs185172198	chr8:34635396-34635397	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs560998153	chr8:34635421-34635422	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs116477082	chr8:34635429-34635430	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs369181995	chr8:34635438-34635439	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs573395421	chr8:34635484-34635485	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs76120632	chr8:34635497-34635498	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs564528588	chr8:34635524-34635525	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs532012655	chr8:34635525-34635526	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs189878827	chr8:34635557-34635558	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs114385283	chr8:34635583-34635584	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs549787839	chr8:34635613-34635614	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs530277732	chr8:34635655-34635656	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs140821840	chr8:34635664-34635665	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs7831242	chr8:34635667-34635668	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs71541887	chr8:34635687-34635688	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs150016610	chr8:34635755-34635756	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs559136523	chr8:34635792-34635793	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs570845268	chr8:34635805-34635806	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:118)

Disease	PMID	Source
Salivary gland tumor	18059337	CNVD
Breast cancer	17133270	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	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
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	21386901	CNVD
Prostate cancer	21088497	CNVD
Prostate cancer	21965145	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
Colorectal cancer	16272173	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
Breast cancer	21509527	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Seminomas	18059402	CNVD
Lung cancer	18438408	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Myxofibrosarcoma	16751306	CNVD
Immune disease	21572526	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Kallmann Syndrome 2	22470819	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Pancreatic cancer	21811587	CNVD
Multiple myeloma	16461302	CNVD
Developmental delay	21373258	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	17603634	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Multiple myeloma	16616336	CNVD
Melanoma	20688739	CNVD
Disorders of sex development	21048976	CNVD
Testicular cancer	18059402	CNVD
Breast cancer	21806811	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hepatocellular carcinoma	16750200	CNVD
Bladder cancer	19088036	CNVD
Urothelial carcinoma	21177765	CNVD
Breast cancer	20459607	CNVD
Renal cell carcinoma	18765545	CNVD
Colorectal cancer	16912164	CNVD
Neuroticism	17667963	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Breast cancer	17001308	CNVD
Breast cancer	17157792	CNVD
Cancer	17001308	CNVD
Cancer	18840272	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Chordoma	18071362	CNVD
Urothelial carcinoma	18382360	CNVD
Ductal carcinoma	18381933	CNVD
Breast cancer	21328542	CNVD
Squamous cell cancer	20885788	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Intellectual disability	22045946	CNVD
Lung cancer	17925434	CNVD
Uveal melanoma	20484589	CNVD
Breast cancer	16608533	CNVD
Breast cancer	21364760	CNVD
Ewing''s sarcoma	17952124	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Renal cell carcinoma	21215367	CNVD

Chromatin state (count:246 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:34634600-34638800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr8:34638600-34639200	Enhancers	HUVEC	blood vessel
3	chr8:34638600-34640200	Enhancers	HMEC	breast
4	chr8:34638800-34639400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr8:34638800-34640000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr8:34639200-34640000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr8:34640000-34640200	Enhancers	Fetal Brain Male	brain
8	chr8:34640200-34641200	Weak transcription	Fetal Brain Male	brain
9	chr8:34641200-34641600	Enhancers	Fetal Brain Male	brain
10	chr8:34641400-34641800	Enhancers	Fetal Brain Female	brain
11	chr8:34657000-34657200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
12	chr8:34657400-34663000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
13	chr8:34663000-34663200	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
14	chr8:34663200-34673000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
15	chr8:34669600-34669800	Enhancers	Brain Hippocampus Middle	brain
16	chr8:34669800-34670200	Enhancers	Brain Angular Gyrus	brain
17	chr8:34669800-34670800	Weak transcription	Brain Hippocampus Middle	brain
18	chr8:34669800-34670800	Enhancers	Brain Substantia Nigra	brain
19	chr8:34670800-34671000	Flanking Active TSS	Brain Hippocampus Middle	brain
20	chr8:34670800-34671200	Active TSS	Brain Substantia Nigra	brain
21	chr8:34671000-34671400	Active TSS	Brain Hippocampus Middle	brain
22	chr8:34673000-34673400	Strong transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
23	chr8:34673000-34673400	ZNF genes & repeats	Pancreas	Pancrea
24	chr8:34673400-34701600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
25	chr8:34675400-34675800	Enhancers	HUES6 Cell Line	embryonic stem cell
26	chr8:34675600-34675800	Enhancers	H9 Cell Line	embryonic stem cell
27	chr8:34675600-34675800	Enhancers	HUES64 Cell Line	embryonic stem cell
28	chr8:34675600-34676000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr8:34675600-34676000	Enhancers	HUES48 Cell Line	embryonic stem cell
30	chr8:34675800-34676000	Enhancers	iPS-18 Cell Line	embryonic stem cell
31	chr8:34675800-34677400	Weak transcription	HUES64 Cell Line	embryonic stem cell
32	chr8:34676000-34677600	Weak transcription	HUES48 Cell Line	embryonic stem cell
33	chr8:34676400-34678400	Enhancers	HUVEC	blood vessel
34	chr8:34677200-34678400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
35	chr8:34677200-34678400	Enhancers	NH-A	brain
36	chr8:34677400-34678400	Enhancers	HUES64 Cell Line	embryonic stem cell
37	chr8:34677400-34678400	Enhancers	iPS-20b Cell Line	embryonic stem cell
38	chr8:34677600-34678200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
39	chr8:34677600-34678200	Enhancers	Brain Germinal Matrix	brain
40	chr8:34677600-34678400	Enhancers	H9 Cell Line	embryonic stem cell
41	chr8:34677600-34678400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr8:34677600-34678400	Enhancers	HUES48 Cell Line	embryonic stem cell
43	chr8:34677600-34678400	Enhancers	iPS-18 Cell Line	embryonic stem cell
44	chr8:34677600-34678400	Enhancers	HMEC	breast
45	chr8:34677800-34678400	Enhancers	Cortex derived primary cultured neurospheres	brain
46	chr8:34684600-34684800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr8:34687000-34687600	Enhancers	HMEC	breast
48	chr8:34687000-34688600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr8:34687200-34687600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
50	chr8:34687600-34688800	Weak transcription	HMEC	breast

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