Variant report

Variant	esv1820362
Chromosome Location	chr8:6828226-6883059
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:51)
CpG islands
(count:427)
Chromatin interactive
region (count:2)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:51 , 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	chr8:6882761-6882780	H1-hESC	embryonic stem cell:	n/a	n/a
4	CEBPB	chr8:6882109-6882181	A549	lung:	n/a	n/a
5	CEBPB	chr8:6872820-6873018	HepG2	liver:	n/a	chr8:6872838-6872849 chr8:6872837-6872848
6	CTCF	chr8:6841333-6841432	GM10248	blood:	n/a	n/a
7	CTCF	chr8:6870668-6870718	Lung_OC	lung:	n/a	n/a
8	CTCF	chr8:6830796-6830848	Lung_OC	lung:	n/a	n/a
9	CTCF	chr8:6850725-6850800	Lung_OC	lung:	n/a	n/a
10	CTCF	chr8:6830206-6830256	Kidney_OC	kidney:	n/a	n/a
11	CTCF	chr8:6829829-6829883	LNCaP	prostate:	n/a	n/a
12	CTCF	chr8:6863352-6863389	GM13977	blood:	n/a	n/a
13	CTCF	chr8:6876641-6876732	GM13976	blood:	n/a	n/a
14	CTCF	chr8:6833327-6833368	Kidney_OC	kidney:	n/a	n/a
15	CTCF	chr8:6832055-6832125	GM13976	blood:	n/a	n/a
16	CTCF	chr8:6829826-6829954	LNCaP	prostate:	n/a	n/a
17	CTCF	chr8:6875862-6875906	Kidney_OC	kidney:	n/a	n/a
18	CTCF	chr8:6829420-6829509	LNCaP	prostate:	n/a	n/a
19	CTCF	chr8:6868755-6868819	GM13976	blood:	n/a	n/a
20	FOS	chr8:6829914-6829972	MCF10A-Er-Src	breast:	n/a	n/a
21	GABPA	chr8:6878604-6878734	Hela-S3	cervix:	n/a	n/a
22	JUN	chr8:6829918-6830101	K562	blood:	n/a	n/a
23	JUN	chr8:6829481-6830053	K562	blood:	n/a	n/a
24	JUND	chr8:6829930-6830012	HepG2	liver:	n/a	n/a
25	JUND	chr8:6829760-6830100	K562	blood:	n/a	n/a
26	JUND	chr8:6829764-6829956	H1-hESC	embryonic stem cell:	n/a	n/a
27	JUND	chr8:6829868-6829984	H1-hESC	embryonic stem cell:	n/a	n/a
28	KAP1	chr8:6829739-6830136	U2OS	brain:	n/a	n/a
29	KAP1	chr8:6829741-6830106	HEK293	kidney:	n/a	n/a
30	MAFF	chr8:6829846-6829893	HepG2	liver:	n/a	n/a
31	MAFK	chr8:6829930-6829935	HepG2	liver:	n/a	n/a
32	MAFK	chr8:6829763-6829959	H1-hESC	embryonic stem cell:	n/a	chr8:6829896-6829907 chr8:6829896-6829907 chr8:6829891-6829906
33	MAFK	chr8:6829943-6829957	Hela-S3	cervix:	n/a	n/a
34	MAFK	chr8:6829787-6829987	HepG2	liver:	n/a	chr8:6829896-6829907 chr8:6829896-6829907 chr8:6829891-6829906
35	POLR2A	chr8:6845770-6845778	MCF-7	breast:	n/a	n/a
36	POLR2A	chr8:6882752-6882809	GM12878	blood:	n/a	n/a
37	POLR2A	chr8:6845727-6845752	MCF-7	breast:	n/a	n/a
38	POLR2A	chr8:6838321-6838399	Gliobla	brain:	n/a	n/a
39	POLR2A	chr8:6857571-6857648	Gliobla	brain:	n/a	n/a
40	SETDB1	chr8:6829763-6830144	U2OS	brain:	n/a	n/a
41	SPI1	chr8:6861083-6861304	GM12891	blood:	n/a	chr8:6861225-6861238
42	SPI1	chr8:6837542-6837676	K562	blood:	n/a	chr8:6837626-6837639
43	SPI1	chr8:6847171-6847347	K562	blood:	n/a	n/a
44	SPI1	chr8:6866274-6866450	K562	blood:	n/a	n/a
45	SPI1	chr8:6841978-6842199	GM12891	blood:	n/a	chr8:6842120-6842133
46	SPI1	chr8:6875751-6875885	K562	blood:	n/a	chr8:6875835-6875848
47	SPI1	chr8:6856652-6856786	K562	blood:	n/a	chr8:6856736-6856749
48	TEAD4	chr8:6843178-6843665	H1-hESC	embryonic stem cell:	n/a	n/a
49	TEAD4	chr8:6862289-6862645	H1-hESC	embryonic stem cell:	n/a	n/a
50	TEAD4	chr8:6843230-6843570	H1-hESC	embryonic stem cell:	n/a	n/a

(count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:6837932-6837982	A549	lung:	n/a
2	chr8:6838024-6838074	A549	lung:	n/a
3	chr8:6838024-6838074	GM12891	blood:	n/a
4	chr8:6876781-6876831	HCM	heart:	n/a
5	chr8:6837932-6837982	HNPCEpiC	eye:	n/a
6	chr8:6876781-6876831	HPAEpiC	pulmonary alveolar:	n/a
7	chr8:6873754-6873804	SK-N-SH	brain:	n/a
8	chr8:6873754-6873804	Jurkat	blood:	n/a
9	chr8:6876695-6876745	K562	blood:	n/a
10	chr8:6876781-6876831	SK-N-MC	brain:	n/a
11	chr8:6875661-6875711	T-47D	breast:	n/a
12	chr8:6838024-6838074	LNCaP	prostate:	n/a
13	chr8:6875661-6875711	ECC-1	luminal epithelium:	n/a
14	chr8:6876155-6876205	HNPCEpiC	eye:	n/a
15	chr8:6875661-6875711	HCT-116	colon:	n/a
16	chr8:6837932-6837982	ProgFib	skin:	n/a
17	chr8:6876695-6876745	HRPEpiC	eye:	n/a
18	chr8:6876781-6876831	Jurkat	blood:	n/a
19	chr8:6876781-6876831	SK-N-SH	brain:	n/a
20	chr8:6837932-6837982	AG09309	skin:	n/a
21	chr8:6876781-6876831	AG10803	skin:	n/a
22	chr8:6876781-6876831	HEEpiC	esophagus:	n/a
23	chr8:6873754-6873804	NB4	blood:	n/a
24	chr8:6873754-6873804	HRPEpiC	eye:	n/a
25	chr8:6838024-6838074	HCF	heart:	n/a
26	chr8:6875661-6875711	GM06990	blood:	n/a
27	chr8:6838024-6838074	AG04449	skin:	fetal
28	chr8:6837932-6837982	HCT-116	colon:	n/a
29	chr8:6876695-6876745	NT2-D1	testis:	n/a
30	chr8:6838024-6838074	H1-hESC	embryonic stem cell:	embryo
31	chr8:6838024-6838074	AG09309	skin:	n/a
32	chr8:6873754-6873804	Caco-2	colon:	n/a
33	chr8:6876155-6876205	A549	lung:	n/a
34	chr8:6875661-6875711	AoSMC	blood vessel:	n/a
35	chr8:6876155-6876205	T-47D	breast:	n/a
36	chr8:6876155-6876205	ProgFib	skin:	n/a
37	chr8:6873754-6873804	IMR90	lung:	fetal
38	chr8:6876155-6876205	SK-N-MC	brain:	n/a
39	chr8:6837932-6837982	Jurkat	blood:	n/a
40	chr8:6875661-6875711	K562	blood:	n/a
41	chr8:6876781-6876831	HRCEpiC	kidney:	n/a
42	chr8:6837932-6837982	HCM	heart:	n/a
43	chr8:6876695-6876745	HEK293	kidney:	embryo
44	chr8:6837932-6837982	GM12891	blood:	n/a
45	chr8:6838024-6838074	Jurkat	blood:	n/a
46	chr8:6876695-6876745	HCPEpiC	choroid plexus:	n/a
47	chr8:6876695-6876745	HepG2	liver:	n/a
48	chr8:6876155-6876205	HCF	heart:	n/a
49	chr8:6875661-6875711	NHBE	bronchial:	n/a
50	chr8:6875661-6875711	MCF10A-Er-Src	breast:	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
DEFA3	TF binding region
DEFT1P	TF binding region
DEFA1B	TF binding region
DEFT1P2	TF binding region
DEFA10P	TF binding region
DEFA1	TF binding region
DEFA3	CpG island
DEFT1P	CpG island
DEFA1B	CpG island
DEFT1P2	CpG island
DEFA10P	CpG island
DEFA1	CpG island

Extended variants
information (count: 1358 )
Associated
traits (count: 141 )

Variant overlapped rSNPs/rCNVs (count:1358 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2978916	chr8:6828241-6828242	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs188924352	chr8:6828268-6828269	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs200934795	chr8:6828280-6828281	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs563880345	chr8:6828306-6828307	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs116962163	chr8:6828318-6828319	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs549648407	chr8:6828367-6828368	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs566271946	chr8:6828382-6828383	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs368934385	chr8:6828388-6828389	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs371296356	chr8:6828421-6828422	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs2615765	chr8:6828431-6828432	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs10088393	chr8:6828435-6828436	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs367879456	chr8:6828440-6828441	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs371660150	chr8:6828463-6828464	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs115374166	chr8:6828520-6828521	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs555901617	chr8:6828529-6828530	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs74759406	chr8:6828555-6828556	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs147460547	chr8:6828582-6828583	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs535930006	chr8:6828584-6828585	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs148480004	chr8:6828606-6828607	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs2615766	chr8:6828609-6828610	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs375660522	chr8:6828610-6828611	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs577769986	chr8:6828621-6828622	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs543532483	chr8:6828622-6828623	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs563420248	chr8:6828631-6828632	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs141801105	chr8:6828634-6828635	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs549347211	chr8:6828637-6828638	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs2615767	chr8:6828647-6828648	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs181975360	chr8:6828659-6828660	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs528804920	chr8:6828660-6828661	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs2927342	chr8:6828667-6828668	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs186354788	chr8:6828669-6828670	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs116044722	chr8:6828670-6828671	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs537089760	chr8:6828679-6828680	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs116350966	chr8:6828684-6828685	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs369531559	chr8:6828713-6828714	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs535600868	chr8:6828717-6828718	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs115348329	chr8:6828730-6828731	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs571451114	chr8:6828757-6828758	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs551825003	chr8:6828761-6828762	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs71525780	chr8:6828766-6828767	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs534923508	chr8:6828770-6828771	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs12682063	chr8:6828781-6828782	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs150557384	chr8:6828785-6828786	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs12682076	chr8:6828791-6828792	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs12675296	chr8:6828795-6828796	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs573670894	chr8:6828810-6828811	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs12675298	chr8:6828813-6828814	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
48	rs559696318	chr8:6828819-6828820	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs73661317	chr8:6828832-6828833	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs545289517	chr8:6828837-6828838	Weak transcription Enhancers	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:32 , 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	chr8:6824800-6829200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr8:6828200-6828600	Enhancers	H1 Cell Line	embryonic stem cell
5	chr8:6828200-6828600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr8:6828400-6828600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
7	chr8:6828600-6829600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr8:6829200-6829400	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr8:6829200-6829400	Enhancers	Right Ventricle	heart
10	chr8:6829200-6830200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr8:6829600-6830000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
12	chr8:6829600-6830000	Enhancers	Fetal Brain Male	brain
13	chr8:6829600-6830200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr8:6829800-6830000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr8:6830000-6833000	Weak transcription	Primary neutrophils fromperipheralblood	blood
16	chr8:6831000-6831200	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
17	chr8:6833000-6833600	Enhancers	Primary neutrophils fromperipheralblood	blood
18	chr8:6833600-6837800	Weak transcription	Primary neutrophils fromperipheralblood	blood
19	chr8:6837800-6838200	Enhancers	Primary neutrophils fromperipheralblood	blood
20	chr8:6838200-6840600	Weak transcription	Primary neutrophils fromperipheralblood	blood
21	chr8:6840600-6841800	Enhancers	Primary neutrophils fromperipheralblood	blood
22	chr8:6856800-6857400	Enhancers	Primary neutrophils fromperipheralblood	blood
23	chr8:6863200-6866800	Weak transcription	Primary neutrophils fromperipheralblood	blood
24	chr8:6867000-6871800	Weak transcription	Primary neutrophils fromperipheralblood	blood
25	chr8:6871800-6873000	Enhancers	Primary neutrophils fromperipheralblood	blood
26	chr8:6872400-6872600	Enhancers	Primary hematopoietic stem cells	blood
27	chr8:6873000-6873400	Weak transcription	Primary neutrophils fromperipheralblood	blood
28	chr8:6873400-6884600	Enhancers	Primary neutrophils fromperipheralblood	blood
29	chr8:6879800-6881200	Enhancers	Dnd41	blood
30	chr8:6881200-6881400	Bivalent Enhancer	ES-WA7 Cell Line	embryonic stem cell
31	chr8:6882000-6882400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr8:6882200-6882400	Enhancers	iPS-15b Cell Line	embryonic stem cell

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