Variant report

Variant	esv1846499
Chromosome Location	chr8:6827068-6879550
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:57)
CpG islands
(count:610)
Chromatin interactive
region (count:1)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:57 , 50 per page) page: 1 2

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	BACH1	chr8:6829927-6829940	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	CTCF	chr8:6827960-6828110	K562	blood:	n/a	n/a
5	CTCF	chr8:6832055-6832125	GM13976	blood:	n/a	n/a
6	CTCF	chr8:6828045-6828050	Gliobla	brain:	n/a	n/a
7	CTCF	chr8:6850725-6850800	Lung_OC	lung:	n/a	n/a
8	CTCF	chr8:6828040-6828190	HepG2	liver:	n/a	n/a
9	CTCF	chr8:6829829-6829883	LNCaP	prostate:	n/a	n/a
10	CTCF	chr8:6829826-6829954	LNCaP	prostate:	n/a	n/a
11	CTCF	chr8:6830796-6830848	Lung_OC	lung:	n/a	n/a
12	CTCF	chr8:6827996-6828116	H1-hESC	embryonic stem cell:	n/a	n/a
13	CTCF	chr8:6876641-6876732	GM13976	blood:	n/a	n/a
14	CTCF	chr8:6841333-6841432	GM10248	blood:	n/a	n/a
15	CTCF	chr8:6870668-6870718	Lung_OC	lung:	n/a	n/a
16	CTCF	chr8:6827880-6828030	HEK293	kidney:	n/a	chr8:6827881-6827890 chr8:6827923-6827930
17	CTCF	chr8:6829420-6829509	LNCaP	prostate:	n/a	n/a
18	CTCF	chr8:6827997-6828044	Gliobla	brain:	n/a	n/a
19	CTCF	chr8:6875862-6875906	Kidney_OC	kidney:	n/a	n/a
20	CTCF	chr8:6863352-6863389	GM13977	blood:	n/a	n/a
21	CTCF	chr8:6827929-6828105	H1-hESC	embryonic stem cell:	n/a	n/a
22	CTCF	chr8:6833327-6833368	Kidney_OC	kidney:	n/a	n/a
23	CTCF	chr8:6830206-6830256	Kidney_OC	kidney:	n/a	n/a
24	CTCF	chr8:6868755-6868819	GM13976	blood:	n/a	n/a
25	FOS	chr8:6829914-6829972	MCF10A-Er-Src	breast:	n/a	n/a
26	GABPA	chr8:6878604-6878734	Hela-S3	cervix:	n/a	n/a
27	JUN	chr8:6829481-6830053	K562	blood:	n/a	n/a
28	JUN	chr8:6829918-6830101	K562	blood:	n/a	n/a
29	JUND	chr8:6829760-6830100	K562	blood:	n/a	n/a
30	JUND	chr8:6829764-6829956	H1-hESC	embryonic stem cell:	n/a	n/a
31	JUND	chr8:6829930-6830012	HepG2	liver:	n/a	n/a
32	JUND	chr8:6829868-6829984	H1-hESC	embryonic stem cell:	n/a	n/a
33	KAP1	chr8:6829739-6830136	U2OS	brain:	n/a	n/a
34	KAP1	chr8:6829741-6830106	HEK293	kidney:	n/a	n/a
35	MAFF	chr8:6829846-6829893	HepG2	liver:	n/a	n/a
36	MAFK	chr8:6829763-6829959	H1-hESC	embryonic stem cell:	n/a	chr8:6829896-6829907 chr8:6829896-6829907 chr8:6829891-6829906
37	MAFK	chr8:6829787-6829987	HepG2	liver:	n/a	chr8:6829896-6829907 chr8:6829896-6829907 chr8:6829891-6829906
38	MAFK	chr8:6829930-6829935	HepG2	liver:	n/a	n/a
39	MAFK	chr8:6829943-6829957	Hela-S3	cervix:	n/a	n/a
40	POLR2A	chr8:6838321-6838399	Gliobla	brain:	n/a	n/a
41	POLR2A	chr8:6845770-6845778	MCF-7	breast:	n/a	n/a
42	POLR2A	chr8:6845727-6845752	MCF-7	breast:	n/a	n/a
43	POLR2A	chr8:6857571-6857648	Gliobla	brain:	n/a	n/a
44	RAD21	chr8:6827832-6828150	H1-hESC	embryonic stem cell:	n/a	n/a
45	SETDB1	chr8:6829763-6830144	U2OS	brain:	n/a	n/a
46	SPI1	chr8:6841978-6842199	GM12891	blood:	n/a	chr8:6842120-6842133
47	SPI1	chr8:6866274-6866450	K562	blood:	n/a	n/a
48	SPI1	chr8:6861083-6861304	GM12891	blood:	n/a	chr8:6861225-6861238
49	SPI1	chr8:6847171-6847347	K562	blood:	n/a	n/a
50	SPI1	chr8:6875751-6875885	K562	blood:	n/a	chr8:6875835-6875848

(count:610 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:6838024-6838074	LNCaP	prostate:	n/a
2	chr8:6828103-6828153	ovcar-3	ovarian:	n/a
3	chr8:6876695-6876745	HEEpiC	esophagus:	n/a
4	chr8:6837932-6837982	K562	blood:	n/a
5	chr8:6827814-6827864	Caco-2	colon:	n/a
6	chr8:6873754-6873804	SAEC	small airway:	n/a
7	chr8:6827800-6827850	HepG2	liver:	n/a
8	chr8:6837932-6837982	HEK293	kidney:	embryo
9	chr8:6838024-6838074	BJ	skin:	n/a
10	chr8:6838024-6838074	PFSK-1	brain:	n/a
11	chr8:6875661-6875711	RPTEC	kidney:	n/a
12	chr8:6837932-6837982	NH-A	brain:	n/a
13	chr8:6828103-6828153	NT2-D1	testis:	n/a
14	chr8:6873754-6873804	AG04449	skin:	fetal
15	chr8:6827800-6827850	NT2-D1	testis:	n/a
16	chr8:6838024-6838074	SKMC	muscle:	n/a
17	chr8:6875661-6875711	A549	lung:	n/a
18	chr8:6875661-6875711	ProgFib	skin:	n/a
19	chr8:6875661-6875711	AG09309	skin:	n/a
20	chr8:6837932-6837982	PANC-1	pancreas:	n/a
21	chr8:6838024-6838074	ovcar-3	ovarian:	n/a
22	chr8:6838024-6838074	HL-60	blood:	n/a
23	chr8:6876155-6876205	Caco-2	colon:	n/a
24	chr8:6873754-6873804	ovcar-3	ovarian:	n/a
25	chr8:6876781-6876831	HEK293	kidney:	embryo
26	chr8:6876155-6876205	ECC-1	luminal epithelium:	n/a
27	chr8:6838024-6838074	BE2_C	brain:	n/a
28	chr8:6876695-6876745	HNPCEpiC	eye:	n/a
29	chr8:6876781-6876831	MCF10A-Er-Src	breast:	n/a
30	chr8:6838024-6838074	NT2-D1	testis:	n/a
31	chr8:6875661-6875711	HPAEpiC	pulmonary alveolar:	n/a
32	chr8:6828103-6828153	HCF	heart:	n/a
33	chr8:6827814-6827864	U87	brain:	n/a
34	chr8:6876155-6876205	K562	blood:	n/a
35	chr8:6837932-6837982	HEEpiC	esophagus:	n/a
36	chr8:6875661-6875711	AoSMC	blood vessel:	n/a
37	chr8:6876781-6876831	HAEpiC	amniotic membrane:	n/a
38	chr8:6876781-6876831	HUVEC	blood vessel:	n/a
39	chr8:6876695-6876745	GM12892	blood:	n/a
40	chr8:6838024-6838074	HAEpiC	amniotic membrane:	n/a
41	chr8:6838024-6838074	HRPEpiC	eye:	n/a
42	chr8:6875661-6875711	NT2-D1	testis:	n/a
43	chr8:6838024-6838074	HCT-116	colon:	n/a
44	chr8:6875661-6875711	H1-hESC	embryonic stem cell:	embryo
45	chr8:6828103-6828153	H1-hESC	embryonic stem cell:	embryo
46	chr8:6838024-6838074	T-47D	breast:	n/a
47	chr8:6876155-6876205	NHBE	bronchial:	n/a
48	chr8:6873754-6873804	SK-N-MC	brain:	n/a
49	chr8:6873754-6873804	U87	brain:	n/a
50	chr8:6838024-6838074	AoSMC	blood vessel:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	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	chr8:6844700-6844945	NONHSAT124804
3	lnc-DEFA1B-1	chr8:6847181-6847243	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: 1179 )
Associated
traits (count: 141 )

Variant overlapped rSNPs/rCNVs (count:1179 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs551709235	chr8:6827069-6827070	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs2978937	chr8:6827127-6827128	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs367701925	chr8:6827129-6827130	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs201077753	chr8:6827138-6827139	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs56203956	chr8:6827143-6827144	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs201726603	chr8:6827148-6827149	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs568177589	chr8:6827154-6827155	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs17078436	chr8:6827165-6827166	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs200286547	chr8:6827192-6827193	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs554362320	chr8:6827205-6827206	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs577440877	chr8:6827223-6827224	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs547199111	chr8:6827292-6827293	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs2738135	chr8:6827299-6827300	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs201678024	chr8:6827301-6827302	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs111492939	chr8:6827329-6827330	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs117455233	chr8:6827394-6827395	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs551109261	chr8:6827404-6827405	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs150455433	chr8:6827426-6827427	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs200379317	chr8:6827438-6827439	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs572516143	chr8:6827478-6827479	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs540024690	chr8:6827479-6827480	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs560296315	chr8:6827517-6827518	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs116966561	chr8:6827534-6827535	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs549167762	chr8:6827575-6827576	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs116781510	chr8:6827606-6827607	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs138288846	chr8:6827617-6827618	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs187212707	chr8:6827618-6827619	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs78147557	chr8:6827633-6827634	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs199792670	chr8:6827644-6827645	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs200536587	chr8:6827658-6827659	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs538287287	chr8:6827678-6827679	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs375179459	chr8:6827689-6827690	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs551788079	chr8:6827690-6827691	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs201307331	chr8:6827695-6827696	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs570792219	chr8:6827708-6827709	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs149584602	chr8:6827710-6827711	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs539333772	chr8:6827716-6827717	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs2977819	chr8:6827740-6827741	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs200722988	chr8:6827748-6827749	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs527404666	chr8:6827767-6827768	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs572919071	chr8:6827768-6827769	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs532469233	chr8:6827776-6827777	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs540082034	chr8:6827780-6827781	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs373405800	chr8:6827784-6827785	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs377576405	chr8:6827794-6827795	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs116642893	chr8:6827814-6827815	Weak transcription Enhancers	CpG island	1 gene(s)	Overlapped CNVs	n/a
47	rs570394622	chr8:6827816-6827817	Weak transcription Enhancers	CpG island	1 gene(s)	Overlapped CNVs	n/a
48	rs192535441	chr8:6827817-6827818	Weak transcription Enhancers	CpG island	1 gene(s)	Overlapped CNVs	n/a
49	rs555751480	chr8:6827818-6827819	Weak transcription Enhancers	CpG island	1 gene(s)	Overlapped CNVs	n/a
50	rs184569436	chr8:6827823-6827824	Weak transcription Enhancers	CpG island	1 gene(s)	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:29 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:6794600-6829200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr8:6822800-6830000	Enhancers	Primary neutrophils fromperipheralblood	blood
3	chr8:6824600-6828200	Weak transcription	H1 Cell Line	embryonic stem cell
4	chr8:6824800-6829200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr8:6828200-6828600	Enhancers	H1 Cell Line	embryonic stem cell
6	chr8:6828200-6828600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr8:6828400-6828600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr8:6828600-6829600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
9	chr8:6829200-6829400	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr8:6829200-6829400	Enhancers	Right Ventricle	heart
11	chr8:6829200-6830200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr8:6829600-6830000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
13	chr8:6829600-6830000	Enhancers	Fetal Brain Male	brain
14	chr8:6829600-6830200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
15	chr8:6829800-6830000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr8:6830000-6833000	Weak transcription	Primary neutrophils fromperipheralblood	blood
17	chr8:6831000-6831200	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
18	chr8:6833000-6833600	Enhancers	Primary neutrophils fromperipheralblood	blood
19	chr8:6833600-6837800	Weak transcription	Primary neutrophils fromperipheralblood	blood
20	chr8:6837800-6838200	Enhancers	Primary neutrophils fromperipheralblood	blood
21	chr8:6838200-6840600	Weak transcription	Primary neutrophils fromperipheralblood	blood
22	chr8:6840600-6841800	Enhancers	Primary neutrophils fromperipheralblood	blood
23	chr8:6856800-6857400	Enhancers	Primary neutrophils fromperipheralblood	blood
24	chr8:6863200-6866800	Weak transcription	Primary neutrophils fromperipheralblood	blood
25	chr8:6867000-6871800	Weak transcription	Primary neutrophils fromperipheralblood	blood
26	chr8:6871800-6873000	Enhancers	Primary neutrophils fromperipheralblood	blood
27	chr8:6872400-6872600	Enhancers	Primary hematopoietic stem cells	blood
28	chr8:6873000-6873400	Weak transcription	Primary neutrophils fromperipheralblood	blood
29	chr8:6873400-6884600	Enhancers	Primary neutrophils fromperipheralblood	blood

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