Variant report

Variant	esv1844176
Chromosome Location	chr8:6823306-6878826
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:72)
CpG islands
(count:671)
Chromatin interactive
region (count:1)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:72 , 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	BHLHE40	chr8:6825706-6825903	K562	blood:	n/a	chr8:6825850-6825859 chr8:6825848-6825857 chr8:6825847-6825860 chr8:6825849-6825858 chr8:6825843-6825864 chr8:6825849-6825858
4	CEBPB	chr8:6872820-6873018	HepG2	liver:	n/a	chr8:6872838-6872849 chr8:6872837-6872848
5	CTCF	chr8:6830206-6830256	Kidney_OC	kidney:	n/a	n/a
6	CTCF	chr8:6829420-6829509	LNCaP	prostate:	n/a	n/a
7	CTCF	chr8:6876641-6876732	GM13976	blood:	n/a	n/a
8	CTCF	chr8:6827929-6828105	H1-hESC	embryonic stem cell:	n/a	n/a
9	CTCF	chr8:6863352-6863389	GM13977	blood:	n/a	n/a
10	CTCF	chr8:6829826-6829954	LNCaP	prostate:	n/a	n/a
11	CTCF	chr8:6870668-6870718	Lung_OC	lung:	n/a	n/a
12	CTCF	chr8:6827960-6828110	K562	blood:	n/a	n/a
13	CTCF	chr8:6832055-6832125	GM13976	blood:	n/a	n/a
14	CTCF	chr8:6868755-6868819	GM13976	blood:	n/a	n/a
15	CTCF	chr8:6850725-6850800	Lung_OC	lung:	n/a	n/a
16	CTCF	chr8:6827880-6828030	HEK293	kidney:	n/a	chr8:6827881-6827890 chr8:6827923-6827930
17	CTCF	chr8:6875862-6875906	Kidney_OC	kidney:	n/a	n/a
18	CTCF	chr8:6828040-6828190	HepG2	liver:	n/a	n/a
19	CTCF	chr8:6830796-6830848	Lung_OC	lung:	n/a	n/a
20	CTCF	chr8:6829829-6829883	LNCaP	prostate:	n/a	n/a
21	CTCF	chr8:6833327-6833368	Kidney_OC	kidney:	n/a	n/a
22	CTCF	chr8:6827996-6828116	H1-hESC	embryonic stem cell:	n/a	n/a
23	CTCF	chr8:6841333-6841432	GM10248	blood:	n/a	n/a
24	CTCF	chr8:6828045-6828050	Gliobla	brain:	n/a	n/a
25	CTCF	chr8:6827997-6828044	Gliobla	brain:	n/a	n/a
26	E2F4	chr8:6823871-6824074	MCF10A-Er-Src	breast:	n/a	n/a
27	ELF1	chr8:6826345-6826676	GM12878	blood:	n/a	n/a
28	FOS	chr8:6829914-6829972	MCF10A-Er-Src	breast:	n/a	n/a
29	GABPA	chr8:6878604-6878734	Hela-S3	cervix:	n/a	n/a
30	JUN	chr8:6829918-6830101	K562	blood:	n/a	n/a
31	JUN	chr8:6829481-6830053	K562	blood:	n/a	n/a
32	JUND	chr8:6829930-6830012	HepG2	liver:	n/a	n/a
33	JUND	chr8:6829868-6829984	H1-hESC	embryonic stem cell:	n/a	n/a
34	JUND	chr8:6829764-6829956	H1-hESC	embryonic stem cell:	n/a	n/a
35	JUND	chr8:6829760-6830100	K562	blood:	n/a	n/a
36	KAP1	chr8:6829739-6830136	U2OS	brain:	n/a	n/a
37	KAP1	chr8:6829741-6830106	HEK293	kidney:	n/a	n/a
38	MAFF	chr8:6829846-6829893	HepG2	liver:	n/a	n/a
39	MAFF	chr8:6825520-6825751	HepG2	liver:	n/a	chr8:6825656-6825674
40	MAFF	chr8:6825659-6825678	K562	blood:	n/a	n/a
41	MAFK	chr8:6829787-6829987	HepG2	liver:	n/a	chr8:6829896-6829907 chr8:6829896-6829907 chr8:6829891-6829906
42	MAFK	chr8:6825552-6825788	IMR90	lung:	n/a	n/a
43	MAFK	chr8:6829930-6829935	HepG2	liver:	n/a	n/a
44	MAFK	chr8:6829943-6829957	Hela-S3	cervix:	n/a	n/a
45	MAFK	chr8:6829763-6829959	H1-hESC	embryonic stem cell:	n/a	chr8:6829896-6829907 chr8:6829896-6829907 chr8:6829891-6829906
46	MAFK	chr8:6825499-6825829	HepG2	liver:	n/a	n/a
47	MAFK	chr8:6825571-6825794	HepG2	liver:	n/a	n/a
48	MAFK	chr8:6825667-6825713	H1-hESC	embryonic stem cell:	n/a	n/a
49	MYC	chr8:6824713-6824802	H1-hESC	embryonic stem cell:	n/a	n/a
50	MYC	chr8:6824687-6824705	H1-hESC	embryonic stem cell:	n/a	n/a

(count:671 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:6827800-6827850	HIPEpiC	eye:	n/a
2	chr8:6828103-6828153	LNCaP	prostate:	n/a
3	chr8:6876155-6876205	SKMC	muscle:	n/a
4	chr8:6873754-6873804	NHDF-neo	bronchial:	n/a
5	chr8:6827800-6827850	SK-N-SH	brain:	n/a
6	chr8:6828103-6828153	SK-N-SH	brain:	n/a
7	chr8:6838024-6838074	SKMC	muscle:	n/a
8	chr8:6838024-6838074	H1-hESC	embryonic stem cell:	embryo
9	chr8:6837932-6837982	HCPEpiC	choroid plexus:	n/a
10	chr8:6828103-6828153	SAEC	small airway:	n/a
11	chr8:6827800-6827850	HRCEpiC	kidney:	n/a
12	chr8:6876781-6876831	AG04450	lung:	fetal
13	chr8:6837932-6837982	HMEC	breast:	n/a
14	chr8:6876155-6876205	NHBE	bronchial:	n/a
15	chr8:6828103-6828153	GM12878	blood:	n/a
16	chr8:6838024-6838074	Hepatocyte	liver:	n/a
17	chr8:6828103-6828153	U87	brain:	n/a
18	chr8:6873754-6873804	HPAEpiC	pulmonary alveolar:	n/a
19	chr8:6828103-6828153	ProgFib	skin:	n/a
20	chr8:6876781-6876831	Jurkat	blood:	n/a
21	chr8:6873754-6873804	A549	lung:	n/a
22	chr8:6827814-6827864	GM19239	blood:	n/a
23	chr8:6828103-6828153	HepG2	liver:	n/a
24	chr8:6876695-6876745	MCF-7	breast:	n/a
25	chr8:6876781-6876831	HCM	heart:	n/a
26	chr8:6827800-6827850	HEK293	kidney:	embryo
27	chr8:6826392-6826442	PrEC	prostate:	n/a
28	chr8:6826392-6826442	LNCaP	prostate:	n/a
29	chr8:6876155-6876205	AG04449	skin:	fetal
30	chr8:6876155-6876205	HNPCEpiC	eye:	n/a
31	chr8:6876695-6876745	GM12892	blood:	n/a
32	chr8:6876781-6876831	IMR90	lung:	fetal
33	chr8:6837932-6837982	GM12891	blood:	n/a
34	chr8:6827814-6827864	HRCEpiC	kidney:	n/a
35	chr8:6827800-6827850	CMK	blood:	n/a
36	chr8:6873754-6873804	HNPCEpiC	eye:	n/a
37	chr8:6827814-6827864	Hela-S3	cervix:	n/a
38	chr8:6826392-6826442	AG04449	skin:	fetal
39	chr8:6837932-6837982	LNCaP	prostate:	n/a
40	chr8:6837932-6837982	HRE	kidney:	n/a
41	chr8:6826392-6826442	GM12891	blood:	n/a
42	chr8:6873754-6873804	U87	brain:	n/a
43	chr8:6876155-6876205	PrEC	prostate:	n/a
44	chr8:6873754-6873804	SK-N-MC	brain:	n/a
45	chr8:6838024-6838074	HEK293	kidney:	embryo
46	chr8:6875661-6875711	IMR90	lung:	fetal
47	chr8:6873754-6873804	PANC-1	pancreas:	n/a
48	chr8:6827800-6827850	Jurkat	blood:	n/a
49	chr8:6827814-6827864	HRE	kidney:	n/a
50	chr8:6827800-6827850	ProgFib	skin:	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:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DEFA1-1	chr8:6826452-6826635	NONHSAT124802
2	lnc-DEFA1-1	chr8:6826461-6826635	NONHSAT124803
3	lnc-DEFA1B-1	chr8:6847181-6847243	NONHSAT124804
4	lnc-DEFA1B-1	chr8:6844700-6844945	NONHSAT124804
5	lnc-DEFA1-1	chr8:6825663-6825769	NONHSAT124802
6	lnc-DEFA1B-1	chr8:6845622-6845808	NONHSAT124804
7	lnc-DEFA1-1	chr8:6825663-6825775	NONHSAT124803

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: 1418 )
Associated
traits (count: 142 )

Variant overlapped rSNPs/rCNVs (count:1418 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs537969142	chr8:6823354-6823355	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs550770482	chr8:6823357-6823358	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs193265008	chr8:6823370-6823371	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs536511352	chr8:6823372-6823373	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs553299847	chr8:6823374-6823375	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs573081605	chr8:6823431-6823432	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs538610803	chr8:6823435-6823436	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs79582267	chr8:6823454-6823455	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs575271008	chr8:6823464-6823465	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs543905857	chr8:6823468-6823469	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs554701327	chr8:6823494-6823495	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs574682571	chr8:6823497-6823498	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs537008035	chr8:6823521-6823522	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs185423814	chr8:6823522-6823523	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs2738046	chr8:6823542-6823543	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
16	rs149972571	chr8:6823551-6823552	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs2702912	chr8:6823565-6823566	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs2738045	chr8:6823568-6823569	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs147256525	chr8:6823571-6823572	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs552783549	chr8:6823575-6823576	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs572692767	chr8:6823609-6823610	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs548713114	chr8:6823615-6823616	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs188246353	chr8:6823626-6823627	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs180946728	chr8:6823638-6823639	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs546848390	chr8:6823663-6823664	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs78566983	chr8:6823698-6823699	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs538575244	chr8:6823766-6823767	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs185022316	chr8:6823770-6823771	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs560708083	chr8:6823783-6823784	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs140608968	chr8:6823788-6823789	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs574752714	chr8:6823790-6823791	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs368164588	chr8:6823791-6823792	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs554239326	chr8:6823805-6823806	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs144546117	chr8:6823811-6823812	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs374227194	chr8:6823827-6823828	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs147820228	chr8:6823831-6823832	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs188728645	chr8:6823851-6823852	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs2702910	chr8:6823891-6823892	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs181100436	chr8:6823907-6823908	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs369963548	chr8:6823927-6823928	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs17078423	chr8:6823933-6823934	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs187000883	chr8:6823937-6823938	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs191439870	chr8:6823959-6823960	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs372788407	chr8:6823970-6823971	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs114071586	chr8:6824010-6824011	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs184123359	chr8:6824018-6824019	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs377310414	chr8:6824035-6824036	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs7005274	chr8:6824042-6824043	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs200237720	chr8:6824052-6824053	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs141300057	chr8:6824065-6824066	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:142)

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
Non-syndromic sensorineural hearing loss	21030649	CNVD
Breast cancer	22522925	CNVD
Autism	21865298	CNVD
Pancreatic cancer	17952125	CNVD
Behcet''s disease	22219625	CNVD
Crohn''s disease	21701837	CNVD

Chromatin state (count:40 , 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	chr8:6824000-6824800	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
4	chr8:6824200-6824600	Enhancers	H1 Cell Line	embryonic stem cell
5	chr8:6824400-6824800	Bivalent Enhancer	Monocytes-CD14+_RO01746	blood
6	chr8:6824600-6824800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr8:6824600-6828200	Weak transcription	H1 Cell Line	embryonic stem cell
8	chr8:6824800-6829200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr8:6826400-6826600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr8:6826400-6826800	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
11	chr8:6826400-6826800	Enhancers	Primary T cells fromperipheralblood	blood
12	chr8:6826400-6826800	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
13	chr8:6826400-6826800	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr8:6826400-6827000	Bivalent Enhancer	Primary B cells from peripheral blood	blood
15	chr8:6826600-6826800	Bivalent Enhancer	Monocytes-CD14+_RO01746	blood
16	chr8:6828200-6828600	Enhancers	H1 Cell Line	embryonic stem cell
17	chr8:6828200-6828600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr8:6828400-6828600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
19	chr8:6828600-6829600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
20	chr8:6829200-6829400	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr8:6829200-6829400	Enhancers	Right Ventricle	heart
22	chr8:6829200-6830200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr8:6829600-6830000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
24	chr8:6829600-6830000	Enhancers	Fetal Brain Male	brain
25	chr8:6829600-6830200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
26	chr8:6829800-6830000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr8:6830000-6833000	Weak transcription	Primary neutrophils fromperipheralblood	blood
28	chr8:6831000-6831200	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
29	chr8:6833000-6833600	Enhancers	Primary neutrophils fromperipheralblood	blood
30	chr8:6833600-6837800	Weak transcription	Primary neutrophils fromperipheralblood	blood
31	chr8:6837800-6838200	Enhancers	Primary neutrophils fromperipheralblood	blood
32	chr8:6838200-6840600	Weak transcription	Primary neutrophils fromperipheralblood	blood
33	chr8:6840600-6841800	Enhancers	Primary neutrophils fromperipheralblood	blood
34	chr8:6856800-6857400	Enhancers	Primary neutrophils fromperipheralblood	blood
35	chr8:6863200-6866800	Weak transcription	Primary neutrophils fromperipheralblood	blood
36	chr8:6867000-6871800	Weak transcription	Primary neutrophils fromperipheralblood	blood
37	chr8:6871800-6873000	Enhancers	Primary neutrophils fromperipheralblood	blood
38	chr8:6872400-6872600	Enhancers	Primary hematopoietic stem cells	blood
39	chr8:6873000-6873400	Weak transcription	Primary neutrophils fromperipheralblood	blood
40	chr8:6873400-6884600	Enhancers	Primary neutrophils fromperipheralblood	blood

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