Variant report

Variant	esv2754662
Chromosome Location	chr8:35558658-35648958
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr8:35637878-35638216	HepG2	liver:	n/a	chr8:35638032-35638041 chr8:35638031-35638042
2	CEBPB	chr8:35641050-35641476	H1-hESC	embryonic stem cell:	n/a	n/a
3	CEBPB	chr8:35587790-35588138	IMR90	lung:	n/a	chr8:35587949-35587960 chr8:35587950-35587959 chr8:35587948-35587961 chr8:35587948-35587959
4	CEBPB	chr8:35587803-35588127	H1-hESC	embryonic stem cell:	n/a	chr8:35587949-35587960 chr8:35587950-35587959 chr8:35587948-35587961 chr8:35587948-35587959
5	CEBPB	chr8:35602643-35602843	HepG2	liver:	n/a	chr8:35602724-35602735
6	CEBPB	chr8:35637869-35638225	IMR90	lung:	n/a	chr8:35638032-35638041 chr8:35638031-35638042
7	CEBPB	chr8:35575000-35575611	H1-hESC	embryonic stem cell:	n/a	n/a
8	CEBPB	chr8:35587780-35588134	HepG2	liver:	n/a	chr8:35587949-35587960 chr8:35587950-35587959 chr8:35587948-35587961 chr8:35587948-35587959
9	CEBPB	chr8:35618307-35618518	A549	lung:	n/a	chr8:35618369-35618382
10	CEBPB	chr8:35643320-35643687	H1-hESC	embryonic stem cell:	n/a	chr8:35643499-35643510
11	CEBPB	chr8:35587784-35588055	K562	blood:	n/a	chr8:35587949-35587960 chr8:35587950-35587959 chr8:35587948-35587961 chr8:35587948-35587959
12	CEBPB	chr8:35643373-35643678	K562	blood:	n/a	chr8:35643499-35643510
13	CEBPB	chr8:35643342-35643712	ECC-1	luminal epithelium:	n/a	chr8:35643499-35643510
14	CEBPB	chr8:35637840-35638217	H1-hESC	embryonic stem cell:	n/a	chr8:35638032-35638041 chr8:35638031-35638042
15	CEBPB	chr8:35643317-35643693	IMR90	lung:	n/a	chr8:35643499-35643510
16	CEBPB	chr8:35637927-35638130	K562	blood:	n/a	chr8:35638032-35638041 chr8:35638031-35638042
17	CEBPB	chr8:35637870-35638208	A549	lung:	n/a	chr8:35638032-35638041 chr8:35638031-35638042
18	CEBPB	chr8:35643318-35643686	HepG2	liver:	n/a	chr8:35643499-35643510
19	CEBPB	chr8:35643368-35643653	ECC-1	luminal epithelium:	n/a	chr8:35643499-35643510
20	CEBPB	chr8:35643317-35643677	Hela-S3	cervix:	n/a	chr8:35643499-35643510
21	CEBPB	chr8:35643317-35643694	A549	lung:	n/a	chr8:35643499-35643510
22	CEBPB	chr8:35587769-35588129	A549	lung:	n/a	chr8:35587949-35587960 chr8:35587950-35587959 chr8:35587948-35587961 chr8:35587948-35587959
23	CTBP2	chr8:35575428-35576630	H1-hESC	embryonic stem cell:	n/a	n/a
24	CTCF	chr8:35622620-35622770	GM12864	blood:	n/a	n/a
25	CTCF	chr8:35622600-35622750	GM06990	blood:	n/a	n/a
26	CTCF	chr8:35622620-35622770	GM12873	blood:	n/a	n/a
27	CTCF	chr8:35622600-35622750	GM12875	blood:	n/a	n/a
28	CTCF	chr8:35622640-35622790	GM12872	blood:	n/a	n/a
29	CTCF	chr8:35577898-35577953	GM13976	blood:	n/a	n/a
30	CTCF	chr8:35622580-35622730	GM12868	blood:	n/a	n/a
31	CTCF	chr8:35622580-35622730	GM12869	blood:	n/a	n/a
32	CTCF	chr8:35622620-35622770	HMEC	breast:	n/a	n/a
33	CTCF	chr8:35622637-35622764	H1-hESC	embryonic stem cell:	n/a	n/a
34	CTCF	chr8:35622660-35622810	AG09319	gingival:	n/a	n/a
35	CTCF	chr8:35622640-35622790	Hela-S3	cervix:	n/a	n/a
36	CTCF	chr8:35622760-35622910	HRE	kidney:	n/a	n/a
37	CTCF	chr8:35622740-35622890	MCF-7	breast:	n/a	n/a
38	CTCF	chr8:35622660-35622810	GM12866	blood:	n/a	n/a
39	CTCF	chr8:35622700-35622850	SAEC	small airway:	n/a	n/a
40	CTCF	chr8:35622760-35622910	NHDF-neo	bronchial:	n/a	n/a
41	CTCF	chr8:35622640-35622790	WERI-Rb-1	eye:	n/a	n/a
42	CTCF	chr8:35622620-35622770	RPTEC	kidney:	n/a	n/a
43	CTCF	chr8:35576229-35576289	H1-hESC	embryonic stem cell:	n/a	n/a
44	CTCF	chr8:35622660-35622810	HepG2	liver:	n/a	n/a
45	CTCF	chr8:35622640-35622790	SK-N-SH_RA	brain:	n/a	n/a
46	CTCF	chr8:35648920-35649070	AG04449	skin:	n/a	n/a
47	CTCF	chr8:35622720-35622870	GM12872	blood:	n/a	n/a
48	CTCF	chr8:35622681-35622879	K562	blood:	n/a	n/a
49	CTCF	chr8:35622600-35622750	GM12871	blood:	n/a	n/a
50	CTCF	chr8:35622680-35622830	GM12874	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:35580715-35580765	HMEC	breast:	n/a
2	chr8:35581526-35581576	NHDF-neo	bronchial:	n/a
3	chr8:35576222-35576272	HCT-116	colon:	n/a
4	chr8:35613299-35613349	AoSMC	blood vessel:	n/a
5	chr8:35613299-35613349	Hepatocyte	liver:	n/a
6	chr8:35580715-35580765	SKMC	muscle:	n/a
7	chr8:35598326-35598376	NHBE	bronchial:	n/a
8	chr8:35581526-35581576	GM12891	blood:	n/a
9	chr8:35581526-35581576	HAEpiC	amniotic membrane:	n/a
10	chr8:35613299-35613349	HNPCEpiC	eye:	n/a
11	chr8:35576222-35576272	NB4	blood:	n/a
12	chr8:35580432-35580482	Hela-S3	cervix:	n/a
13	chr8:35576222-35576272	AoSMC	blood vessel:	n/a
14	chr8:35580715-35580765	AG04449	skin:	fetal
15	chr8:35581526-35581576	HRE	kidney:	n/a
16	chr8:35580715-35580765	AG09309	skin:	n/a
17	chr8:35598326-35598376	HCF	heart:	n/a
18	chr8:35598326-35598376	PrEC	prostate:	n/a
19	chr8:35598326-35598376	HRCEpiC	kidney:	n/a
20	chr8:35580432-35580482	SK-N-MC	brain:	n/a
21	chr8:35581526-35581576	GM12878	blood:	n/a
22	chr8:35580432-35580482	SK-N-SH	brain:	n/a
23	chr8:35576222-35576272	HEK293	kidney:	embryo
24	chr8:35613299-35613349	SKMC	muscle:	n/a
25	chr8:35613299-35613349	AG09309	skin:	n/a
26	chr8:35581526-35581576	A549	lung:	n/a
27	chr8:35581526-35581576	AG10803	skin:	n/a
28	chr8:35613299-35613349	HEK293	kidney:	embryo
29	chr8:35580715-35580765	Caco-2	colon:	n/a
30	chr8:35598326-35598376	AG04449	skin:	fetal
31	chr8:35613299-35613349	U87	brain:	n/a
32	chr8:35613299-35613349	SAEC	small airway:	n/a
33	chr8:35598326-35598376	K562	blood:	n/a
34	chr8:35598326-35598376	GM12891	blood:	n/a
35	chr8:35576222-35576272	SK-N-SH_RA	brain:	n/a
36	chr8:35580715-35580765	GM19239	blood:	n/a
37	chr8:35613299-35613349	Jurkat	blood:	n/a
38	chr8:35580432-35580482	SKMC	muscle:	n/a
39	chr8:35581526-35581576	HEEpiC	esophagus:	n/a
40	chr8:35613299-35613349	HRE	kidney:	n/a
41	chr8:35576222-35576272	H1-hESC	embryonic stem cell:	embryo
42	chr8:35613299-35613349	HCPEpiC	choroid plexus:	n/a
43	chr8:35613299-35613349	HMEC	breast:	n/a
44	chr8:35576222-35576272	U87	brain:	n/a
45	chr8:35613299-35613349	ovcar-3	ovarian:	n/a
46	chr8:35580715-35580765	U87	brain:	n/a
47	chr8:35580432-35580482	GM06990	blood:	n/a
48	chr8:35576222-35576272	HEEpiC	esophagus:	n/a
49	chr8:35598326-35598376	NH-A	brain:	n/a
50	chr8:35581526-35581576	GM19239	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr8:35620195..35622822-chr8:35626883..35629554,2	K562	blood:
2	chr8:35596968..35598886-chr8:35604620..35606278,2	K562	blood:
3	chr8:35638386..35640452-chr8:35642289..35644463,2	K562	blood:
4	chr8:35620195..35622822-chr8:35626883..35629554,2	K562	blood:
5	chr8:35497530..35499054-chr8:35564853..35566842,2	K562	blood:
6	chr8:35638386..35640452-chr8:35642289..35644463,2	K562	blood:
7	chr8:35596968..35598886-chr8:35604620..35606278,2	K562	blood:

Variant related genes	Relation type
UNC5D	TF binding region
ENSG00000233863	TF binding region
UNC5D	CpG island
ENSG00000233863	CpG island

Extended variants
information (count: 3187 )
Associated
traits (count: 119 )

Variant overlapped rSNPs/rCNVs (count:3187 , 50 per page) page: 1 2 3 4 5 6 7 ... 64

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs192384027	chr8:35558658-35558659	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs565923697	chr8:35558665-35558666	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs536491292	chr8:35558721-35558722	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs183949147	chr8:35558722-35558723	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs563998797	chr8:35558769-35558770	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs576698275	chr8:35558788-35558789	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs543371653	chr8:35558793-35558794	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs558607970	chr8:35558898-35558899	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs576966387	chr8:35558911-35558912	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs541139034	chr8:35558932-35558933	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs188900332	chr8:35558940-35558941	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs529897832	chr8:35558947-35558948	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs368957020	chr8:35559002-35559003	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs147394918	chr8:35559059-35559060	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs541688888	chr8:35559125-35559126	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs531095870	chr8:35559146-35559147	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs530732681	chr8:35559163-35559164	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs72634975	chr8:35559172-35559173	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs73583049	chr8:35559252-35559253	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs532409405	chr8:35559298-35559299	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs547480765	chr8:35559327-35559328	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs16884255	chr8:35559334-35559335	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs146334392	chr8:35559360-35559361	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs193081675	chr8:35559364-35559365	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs184700036	chr8:35559466-35559467	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs139650839	chr8:35559565-35559566	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs558547972	chr8:35559597-35559598	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs576899506	chr8:35559617-35559618	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs534652723	chr8:35559761-35559762	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs553083528	chr8:35559848-35559849	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs574484138	chr8:35559875-35559876	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs541976466	chr8:35559901-35559902	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs563338616	chr8:35559912-35559913	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs535119236	chr8:35559923-35559924	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs12549774	chr8:35559933-35559934	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs115116506	chr8:35559936-35559937	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs564084339	chr8:35559939-35559940	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs532349447	chr8:35559974-35559975	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs149929215	chr8:35559976-35559977	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs187518601	chr8:35559984-35559985	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs191638448	chr8:35559989-35559990	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs114126803	chr8:35560007-35560008	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs184221132	chr8:35560014-35560015	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs537692822	chr8:35560023-35560024	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs145024541	chr8:35560101-35560102	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs16884258	chr8:35560138-35560139	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs556719093	chr8:35560156-35560157	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs551421758	chr8:35560181-35560182	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs115119062	chr8:35560219-35560220	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs112963714	chr8:35560220-35560221	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:119)

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
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
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
Breast cancer	21785460	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:496 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:35530200-35562800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr8:35531000-35579600	Weak transcription	Fetal Brain Female	brain
3	chr8:35538000-35575200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
4	chr8:35542400-35563800	Weak transcription	H9 Cell Line	embryonic stem cell
5	chr8:35544200-35563600	Weak transcription	H1 Cell Line	embryonic stem cell
6	chr8:35545200-35563800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
7	chr8:35547000-35564000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
8	chr8:35547200-35563400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
9	chr8:35547400-35579800	Weak transcription	Cortex derived primary cultured neurospheres	brain
10	chr8:35547600-35563800	Weak transcription	HUES48 Cell Line	embryonic stem cell
11	chr8:35547800-35561800	Weak transcription	HUES6 Cell Line	embryonic stem cell
12	chr8:35547800-35563400	Weak transcription	HUES64 Cell Line	embryonic stem cell
13	chr8:35550600-35562000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr8:35561800-35562200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
15	chr8:35561800-35562400	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
16	chr8:35562000-35565400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr8:35563400-35565000	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
18	chr8:35563400-35565200	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
19	chr8:35563600-35564200	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
20	chr8:35563800-35564000	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
21	chr8:35563800-35564200	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
22	chr8:35563800-35564600	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
23	chr8:35563800-35565400	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
24	chr8:35564000-35564200	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
25	chr8:35564000-35573400	Weak transcription	H9 Cell Line	embryonic stem cell
26	chr8:35564200-35564800	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
27	chr8:35564200-35565200	Strong transcription	H1 Cell Line	embryonic stem cell
28	chr8:35564800-35573400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
29	chr8:35565000-35573400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
30	chr8:35565200-35573600	Weak transcription	H1 Cell Line	embryonic stem cell
31	chr8:35565200-35573800	Weak transcription	HUES64 Cell Line	embryonic stem cell
32	chr8:35565400-35576200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
33	chr8:35570000-35570400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
34	chr8:35570000-35570400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr8:35570400-35575200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
36	chr8:35570400-35575200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr8:35572800-35573000	Enhancers	Stomach Mucosa	stomach
38	chr8:35573400-35576600	Enhancers	H9 Cell Line	embryonic stem cell
39	chr8:35573400-35577000	Enhancers	ES-I3 Cell Line	embryonic stem cell
40	chr8:35573400-35577000	Enhancers	HUES6 Cell Line	embryonic stem cell
41	chr8:35573400-35577800	Enhancers	iPS-20b Cell Line	embryonic stem cell
42	chr8:35573600-35574600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
43	chr8:35573600-35577200	Enhancers	H1 Cell Line	embryonic stem cell
44	chr8:35573800-35577000	Enhancers	HUES64 Cell Line	embryonic stem cell
45	chr8:35573800-35577000	Enhancers	iPS-18 Cell Line	embryonic stem cell
46	chr8:35573800-35578000	Enhancers	HUES48 Cell Line	embryonic stem cell
47	chr8:35574200-35575000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
48	chr8:35574200-35577000	Enhancers	iPS-15b Cell Line	embryonic stem cell
49	chr8:35574200-35577200	Enhancers	Fetal Lung	lung
50	chr8:35574600-35575200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell

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