Variant report

Variant	esv1828947
Chromosome Location	chr8:6829990-6883662
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:40)
CpG islands
(count:428)
Chromatin interactive
region (count:2)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:40 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr8:6829807-6830004	K562	blood:	n/a	n/a
2	CEBPB	chr8:6882761-6882780	H1-hESC	embryonic stem cell:	n/a	n/a
3	CEBPB	chr8:6872820-6873018	HepG2	liver:	n/a	chr8:6872838-6872849 chr8:6872837-6872848
4	CEBPB	chr8:6882109-6882181	A549	lung:	n/a	n/a
5	CTCF	chr8:6868755-6868819	GM13976	blood:	n/a	n/a
6	CTCF	chr8:6830206-6830256	Kidney_OC	kidney:	n/a	n/a
7	CTCF	chr8:6850725-6850800	Lung_OC	lung:	n/a	n/a
8	CTCF	chr8:6832055-6832125	GM13976	blood:	n/a	n/a
9	CTCF	chr8:6841333-6841432	GM10248	blood:	n/a	n/a
10	CTCF	chr8:6870668-6870718	Lung_OC	lung:	n/a	n/a
11	CTCF	chr8:6863352-6863389	GM13977	blood:	n/a	n/a
12	CTCF	chr8:6875862-6875906	Kidney_OC	kidney:	n/a	n/a
13	CTCF	chr8:6883380-6883530	GM12873	blood:	n/a	n/a
14	CTCF	chr8:6830796-6830848	Lung_OC	lung:	n/a	n/a
15	CTCF	chr8:6876641-6876732	GM13976	blood:	n/a	n/a
16	CTCF	chr8:6833327-6833368	Kidney_OC	kidney:	n/a	n/a
17	GABPA	chr8:6878604-6878734	Hela-S3	cervix:	n/a	n/a
18	JUN	chr8:6829918-6830101	K562	blood:	n/a	n/a
19	JUN	chr8:6829481-6830053	K562	blood:	n/a	n/a
20	JUND	chr8:6829760-6830100	K562	blood:	n/a	n/a
21	JUND	chr8:6829930-6830012	HepG2	liver:	n/a	n/a
22	KAP1	chr8:6829739-6830136	U2OS	brain:	n/a	n/a
23	KAP1	chr8:6829741-6830106	HEK293	kidney:	n/a	n/a
24	POLR2A	chr8:6845727-6845752	MCF-7	breast:	n/a	n/a
25	POLR2A	chr8:6845770-6845778	MCF-7	breast:	n/a	n/a
26	POLR2A	chr8:6838321-6838399	Gliobla	brain:	n/a	n/a
27	POLR2A	chr8:6857571-6857648	Gliobla	brain:	n/a	n/a
28	POLR2A	chr8:6882752-6882809	GM12878	blood:	n/a	n/a
29	SETDB1	chr8:6829763-6830144	U2OS	brain:	n/a	n/a
30	SPI1	chr8:6861083-6861304	GM12891	blood:	n/a	chr8:6861225-6861238
31	SPI1	chr8:6866274-6866450	K562	blood:	n/a	n/a
32	SPI1	chr8:6847171-6847347	K562	blood:	n/a	n/a
33	SPI1	chr8:6856652-6856786	K562	blood:	n/a	chr8:6856736-6856749
34	SPI1	chr8:6875751-6875885	K562	blood:	n/a	chr8:6875835-6875848
35	SPI1	chr8:6837542-6837676	K562	blood:	n/a	chr8:6837626-6837639
36	SPI1	chr8:6841978-6842199	GM12891	blood:	n/a	chr8:6842120-6842133
37	TEAD4	chr8:6862289-6862645	H1-hESC	embryonic stem cell:	n/a	n/a
38	TEAD4	chr8:6843230-6843570	H1-hESC	embryonic stem cell:	n/a	n/a
39	TEAD4	chr8:6862289-6862677	H1-hESC	embryonic stem cell:	n/a	n/a
40	TEAD4	chr8:6843178-6843665	H1-hESC	embryonic stem cell:	n/a	n/a

(count:428 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:6876781-6876831	HepG2	liver:	n/a
2	chr8:6876781-6876831	HepG2	liver:	n/a
3	chr8:6873754-6873804	Hepatocyte	liver:	n/a
4	chr8:6876155-6876205	HAEpiC	amniotic membrane:	n/a
5	chr8:6838024-6838074	K562	blood:	n/a
6	chr8:6876695-6876745	BE2_C	brain:	n/a
7	chr8:6875661-6875711	NHBE	bronchial:	n/a
8	chr8:6838024-6838074	HMEC	breast:	n/a
9	chr8:6875661-6875711	HCPEpiC	choroid plexus:	n/a
10	chr8:6876695-6876745	PFSK-1	brain:	n/a
11	chr8:6873754-6873804	PrEC	prostate:	n/a
12	chr8:6875661-6875711	AG04450	lung:	fetal
13	chr8:6876155-6876205	Hela-S3	cervix:	n/a
14	chr8:6876695-6876745	MCF-7	breast:	n/a
15	chr8:6873754-6873804	AG09319	gingival:	n/a
16	chr8:6873754-6873804	NHDF-neo	bronchial:	n/a
17	chr8:6876781-6876831	AG09319	gingival:	n/a
18	chr8:6837932-6837982	HPAEpiC	pulmonary alveolar:	n/a
19	chr8:6876695-6876745	ovcar-3	ovarian:	n/a
20	chr8:6838024-6838074	Jurkat	blood:	n/a
21	chr8:6837932-6837982	HUVEC	blood vessel:	n/a
22	chr8:6876695-6876745	SK-N-MC	brain:	n/a
23	chr8:6876695-6876745	PANC-1	pancreas:	n/a
24	chr8:6876695-6876745	HEK293	kidney:	embryo
25	chr8:6837932-6837982	HMEC	breast:	n/a
26	chr8:6876781-6876831	SK-N-SH	brain:	n/a
27	chr8:6837932-6837982	HAEpiC	amniotic membrane:	n/a
28	chr8:6876695-6876745	NB4	blood:	n/a
29	chr8:6838024-6838074	AG04449	skin:	fetal
30	chr8:6875661-6875711	NT2-D1	testis:	n/a
31	chr8:6838024-6838074	RPTEC	kidney:	n/a
32	chr8:6876781-6876831	SK-N-SH_RA	brain:	n/a
33	chr8:6876695-6876745	HCPEpiC	choroid plexus:	n/a
34	chr8:6873754-6873804	MCF10A-Er-Src	breast:	n/a
35	chr8:6876155-6876205	Jurkat	blood:	n/a
36	chr8:6873754-6873804	HepG2	liver:	n/a
37	chr8:6876155-6876205	SKMC	muscle:	n/a
38	chr8:6875661-6875711	Hela-S3	cervix:	n/a
39	chr8:6876155-6876205	U87	brain:	n/a
40	chr8:6876781-6876831	HRE	kidney:	n/a
41	chr8:6876695-6876745	HepG2	liver:	n/a
42	chr8:6837932-6837982	AoSMC	blood vessel:	n/a
43	chr8:6876155-6876205	GM12892	blood:	n/a
44	chr8:6876781-6876831	AG10803	skin:	n/a
45	chr8:6838024-6838074	GM12878	blood:	n/a
46	chr8:6837932-6837982	U87	brain:	n/a
47	chr8:6876781-6876831	SAEC	small airway:	n/a
48	chr8:6876155-6876205	LNCaP	prostate:	n/a
49	chr8:6876695-6876745	SK-N-SH	brain:	n/a
50	chr8:6876695-6876745	HCM	heart:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:6876740..6878297-chr8:6880024..6881649,2	K562	blood:
2	chr8:6876740..6878297-chr8:6880024..6881649,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DEFA1B-1	chr8:6845622-6845808	NONHSAT124804
2	lnc-DEFA1B-1	chr8:6847181-6847243	NONHSAT124804
3	lnc-DEFA1B-1	chr8:6844700-6844945	NONHSAT124804

No data

Variant related genes	Relation type
DEFA1B	TF binding region
DEFT1P2	TF binding region
DEFA10P	TF binding region
DEFA1	TF binding region
DEFA3	TF binding region
DEFT1P	TF binding region
DEFA1B	CpG island
DEFT1P2	CpG island
DEFA10P	CpG island
DEFA1	CpG island
DEFA3	CpG island
DEFT1P	CpG island

Extended variants
information (count: 1249 )
Associated
traits (count: 141 )

Variant overlapped rSNPs/rCNVs (count:1249 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs535859888	chr8:6829992-6829993	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs57466375	chr8:6829993-6829994	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs80338081	chr8:6830002-6830003	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs2978911	chr8:6830003-6830004	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs10096781	chr8:6830008-6830009	Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs62488543	chr8:6830019-6830020	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs377094072	chr8:6830026-6830027	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs373394130	chr8:6830027-6830028	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs2978910	chr8:6830028-6830029	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs2702916	chr8:6830036-6830037	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs528841929	chr8:6830042-6830043	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs369520579	chr8:6830067-6830068	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs28580279	chr8:6830071-6830072	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs566204484	chr8:6830081-6830082	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs113786932	chr8:6830116-6830117	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs538365306	chr8:6830129-6830130	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs72494231	chr8:6830154-6830155	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs201225338	chr8:6830169-6830170	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs139629992	chr8:6830170-6830171	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs146318068	chr8:6830175-6830176	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs565884305	chr8:6830177-6830178	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs76772439	chr8:6830187-6830188	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs370931658	chr8:6830193-6830194	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs575412680	chr8:6830233-6830234	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs149023260	chr8:6830317-6830318	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs143829625	chr8:6830357-6830358	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs146621847	chr8:6830405-6830406	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs141356385	chr8:6830406-6830407	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs575088350	chr8:6830450-6830451	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs540215521	chr8:6830452-6830453	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs145131487	chr8:6830455-6830456	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs138963616	chr8:6830492-6830493	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs202031032	chr8:6830504-6830505	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs140514903	chr8:6830508-6830509	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs2615786	chr8:6830515-6830516	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs138157150	chr8:6830517-6830518	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs560495814	chr8:6830550-6830551	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs367897889	chr8:6830638-6830639	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs118157794	chr8:6830648-6830649	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs577375994	chr8:6830650-6830651	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs374101949	chr8:6830661-6830662	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs199877148	chr8:6830682-6830683	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs546302813	chr8:6830705-6830706	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs562996489	chr8:6830751-6830752	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs202008160	chr8:6830808-6830809	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs530613530	chr8:6830867-6830868	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs112383345	chr8:6830930-6830931	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs2738091	chr8:6830947-6830948	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs62488544	chr8:6830951-6830952	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs371525953	chr8:6830952-6830953	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:141)

Disease	PMID	Source
Ovarian clear cell carcinoma	21343371	CNVD
abnormal development	18461090	CNVD
Crohn''s disease	19220326	CNVD
Psoriasis	19220326	CNVD
Prostate cancer	21965145	CNVD
Prostate cancer	18515986	CNVD
Chronic obstructive pulmonary disease	20378733	CNVD
Autism	18414403	CNVD
Cancer	21183584	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Breast cancer	17603634	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Ovarian cancer	20844748	CNVD
Cervical cancer	17311676	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Schizophrenia	20877625	CNVD
Disorders of sex development	21048976	CNVD
Colorectal cancer	16272173	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Breast cancer	17001317	CNVD
Thyroid cancer	19087340	CNVD
Multiple myeloma	16616336	CNVD
Hepatocellular carcinoma	22174799	CNVD
Heart disease	21282601	CNVD
Prostate cancer	16573809	CNVD
T-cell lymphomas	19863542	CNVD
Ovarian cancer	22174824	CNVD
Colorectal cancer	21297112	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	17133270	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
Oral cancer	21386901	CNVD
Prostate cancer	21088497	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
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
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Epilepsy	22083797	CNVD
Acute myeloid leukemia	21251322	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Congenital diaphragmatic hernia	21064195	CNVD
Autism	22495311	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16608533	CNVD
Seminomas	18059402	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Colorectal cancer	16774939	CNVD
Breast cancer	21364760	CNVD
Lung squamous cell carcinoma	22363434	CNVD
Cancer	20164919	CNVD
Medulloblastoma	16783165	CNVD
Gastric cancer	18160780	CNVD
Breast cancer	21990379	CNVD
Psoriasis	20403174	CNVD
Psoriasis	20663923	CNVD
Crohn''s disease	16909382	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Crohn''s disease	20877625	CNVD
Inflammatory disorder	20877625	CNVD
Cardiac defect	21933911	CNVD
Psoriasis	18059266	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Psoriasis	20877625	CNVD
Mental retardation	17847001	CNVD
Prostate cancer	17217626	CNVD
Schizophrenia	21399695	CNVD
Colorectal cancer	21128281	CNVD
Colorectal cancer	19455253	CNVD
Psoriasis	18848619	CNVD
Squamous cell cancer	19047905	CNVD
Colorectal cancer	17229543	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Bladder cancer	21909424	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Cognitive impairment	21505072	CNVD
Breast cancer	17142309	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Autism	21865298	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Behcet''s disease	22219625	CNVD
Crohn''s disease	21701837	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:6822800-6830000	Enhancers	Primary neutrophils fromperipheralblood	blood
2	chr8:6829200-6830200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr8:6829600-6830000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr8:6829600-6830000	Enhancers	Fetal Brain Male	brain
5	chr8:6829600-6830200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
6	chr8:6829800-6830000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr8:6830000-6833000	Weak transcription	Primary neutrophils fromperipheralblood	blood
8	chr8:6831000-6831200	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
9	chr8:6833000-6833600	Enhancers	Primary neutrophils fromperipheralblood	blood
10	chr8:6833600-6837800	Weak transcription	Primary neutrophils fromperipheralblood	blood
11	chr8:6837800-6838200	Enhancers	Primary neutrophils fromperipheralblood	blood
12	chr8:6838200-6840600	Weak transcription	Primary neutrophils fromperipheralblood	blood
13	chr8:6840600-6841800	Enhancers	Primary neutrophils fromperipheralblood	blood
14	chr8:6856800-6857400	Enhancers	Primary neutrophils fromperipheralblood	blood
15	chr8:6863200-6866800	Weak transcription	Primary neutrophils fromperipheralblood	blood
16	chr8:6867000-6871800	Weak transcription	Primary neutrophils fromperipheralblood	blood
17	chr8:6871800-6873000	Enhancers	Primary neutrophils fromperipheralblood	blood
18	chr8:6872400-6872600	Enhancers	Primary hematopoietic stem cells	blood
19	chr8:6873000-6873400	Weak transcription	Primary neutrophils fromperipheralblood	blood
20	chr8:6873400-6884600	Enhancers	Primary neutrophils fromperipheralblood	blood
21	chr8:6879800-6881200	Enhancers	Dnd41	blood
22	chr8:6881200-6881400	Bivalent Enhancer	ES-WA7 Cell Line	embryonic stem cell
23	chr8:6882000-6882400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr8:6882200-6882400	Enhancers	iPS-15b Cell Line	embryonic stem cell
25	chr8:6883200-6883400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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