Variant report

Variant	esv1805261
Chromosome Location	chr8:6818594-6878826
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:76)
CpG islands
(count:671)
Chromatin interactive
region (count:2)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:76 , 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	chr8:6876641-6876732	GM13976	blood:	n/a	n/a
6	CTCF	chr8:6827997-6828044	Gliobla	brain:	n/a	n/a
7	CTCF	chr8:6829829-6829883	LNCaP	prostate:	n/a	n/a
8	CTCF	chr8:6875862-6875906	Kidney_OC	kidney:	n/a	n/a
9	CTCF	chr8:6850725-6850800	Lung_OC	lung:	n/a	n/a
10	CTCF	chr8:6827929-6828105	H1-hESC	embryonic stem cell:	n/a	n/a
11	CTCF	chr8:6827960-6828110	K562	blood:	n/a	n/a
12	CTCF	chr8:6868755-6868819	GM13976	blood:	n/a	n/a
13	CTCF	chr8:6841333-6841432	GM10248	blood:	n/a	n/a
14	CTCF	chr8:6832055-6832125	GM13976	blood:	n/a	n/a
15	CTCF	chr8:6827996-6828116	H1-hESC	embryonic stem cell:	n/a	n/a
16	CTCF	chr8:6830206-6830256	Kidney_OC	kidney:	n/a	n/a
17	CTCF	chr8:6829826-6829954	LNCaP	prostate:	n/a	n/a
18	CTCF	chr8:6827880-6828030	HEK293	kidney:	n/a	chr8:6827881-6827890 chr8:6827923-6827930
19	CTCF	chr8:6828040-6828190	HepG2	liver:	n/a	n/a
20	CTCF	chr8:6830796-6830848	Lung_OC	lung:	n/a	n/a
21	CTCF	chr8:6829420-6829509	LNCaP	prostate:	n/a	n/a
22	CTCF	chr8:6863352-6863389	GM13977	blood:	n/a	n/a
23	CTCF	chr8:6828045-6828050	Gliobla	brain:	n/a	n/a
24	CTCF	chr8:6870668-6870718	Lung_OC	lung:	n/a	n/a
25	CTCF	chr8:6833327-6833368	Kidney_OC	kidney:	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	chr8:6829481-6830053	K562	blood:	n/a	n/a
31	JUN	chr8:6829918-6830101	K562	blood:	n/a	n/a
32	JUND	chr8:6829764-6829956	H1-hESC	embryonic stem cell:	n/a	n/a
33	JUND	chr8:6829760-6830100	K562	blood:	n/a	n/a
34	JUND	chr8:6829868-6829984	H1-hESC	embryonic stem cell:	n/a	n/a
35	JUND	chr8:6829930-6830012	HepG2	liver:	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	chr8:6825659-6825678	K562	blood:	n/a	n/a
39	MAFF	chr8:6829846-6829893	HepG2	liver:	n/a	n/a
40	MAFF	chr8:6818690-6818696	HepG2	liver:	n/a	n/a
41	MAFF	chr8:6825520-6825751	HepG2	liver:	n/a	chr8:6825656-6825674
42	MAFK	chr8:6825667-6825713	H1-hESC	embryonic stem cell:	n/a	n/a
43	MAFK	chr8:6829943-6829957	Hela-S3	cervix:	n/a	n/a
44	MAFK	chr8:6818670-6818736	HepG2	liver:	n/a	n/a
45	MAFK	chr8:6825552-6825788	IMR90	lung:	n/a	n/a
46	MAFK	chr8:6829763-6829959	H1-hESC	embryonic stem cell:	n/a	chr8:6829896-6829907 chr8:6829896-6829907 chr8:6829891-6829906
47	MAFK	chr8:6825571-6825794	HepG2	liver:	n/a	n/a
48	MAFK	chr8:6821864-6821951	HepG2	liver:	n/a	chr8:6821896-6821907 chr8:6821891-6821906 chr8:6821891-6821907 chr8:6821896-6821907 chr8:6821895-6821906 chr8:6821894-6821908
49	MAFK	chr8:6825499-6825829	HepG2	liver:	n/a	n/a
50	MAFK	chr8:6829787-6829987	HepG2	liver:	n/a	chr8:6829896-6829907 chr8:6829896-6829907 chr8:6829891-6829906

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:6873754-6873804	AG04449	skin:	fetal
2	chr8:6827814-6827864	GM06990	blood:	n/a
3	chr8:6837932-6837982	PFSK-1	brain:	n/a
4	chr8:6876781-6876831	ProgFib	skin:	n/a
5	chr8:6837932-6837982	AG09309	skin:	n/a
6	chr8:6876155-6876205	HepG2	liver:	n/a
7	chr8:6827814-6827864	HIPEpiC	eye:	n/a
8	chr8:6876695-6876745	HRE	kidney:	n/a
9	chr8:6826392-6826442	HEK293	kidney:	embryo
10	chr8:6837932-6837982	U87	brain:	n/a
11	chr8:6828103-6828153	GM12892	blood:	n/a
12	chr8:6876781-6876831	PFSK-1	brain:	n/a
13	chr8:6828103-6828153	ovcar-3	ovarian:	n/a
14	chr8:6826392-6826442	HRE	kidney:	n/a
15	chr8:6875661-6875711	CMK	blood:	n/a
16	chr8:6875661-6875711	A549	lung:	n/a
17	chr8:6876695-6876745	A549	lung:	n/a
18	chr8:6837932-6837982	HepG2	liver:	n/a
19	chr8:6873754-6873804	PrEC	prostate:	n/a
20	chr8:6837932-6837982	Hepatocyte	liver:	n/a
21	chr8:6876155-6876205	RPTEC	kidney:	n/a
22	chr8:6876155-6876205	U87	brain:	n/a
23	chr8:6876781-6876831	HEEpiC	esophagus:	n/a
24	chr8:6827814-6827864	HAEpiC	amniotic membrane:	n/a
25	chr8:6828103-6828153	IMR90	lung:	fetal
26	chr8:6876695-6876745	MCF10A-Er-Src	breast:	n/a
27	chr8:6876781-6876831	Caco-2	colon:	n/a
28	chr8:6827814-6827864	H1-hESC	embryonic stem cell:	embryo
29	chr8:6876695-6876745	GM06990	blood:	n/a
30	chr8:6828103-6828153	HRE	kidney:	n/a
31	chr8:6828103-6828153	AoSMC	blood vessel:	n/a
32	chr8:6873754-6873804	GM12891	blood:	n/a
33	chr8:6876155-6876205	HEK293	kidney:	embryo
34	chr8:6838024-6838074	HL-60	blood:	n/a
35	chr8:6838024-6838074	SK-N-MC	brain:	n/a
36	chr8:6876695-6876745	CMK	blood:	n/a
37	chr8:6826392-6826442	PrEC	prostate:	n/a
38	chr8:6827800-6827850	HepG2	liver:	n/a
39	chr8:6876695-6876745	SK-N-SH_RA	brain:	n/a
40	chr8:6876781-6876831	HPAEpiC	pulmonary alveolar:	n/a
41	chr8:6876695-6876745	Hela-S3	cervix:	n/a
42	chr8:6876155-6876205	IMR90	lung:	fetal
43	chr8:6827814-6827864	AoSMC	blood vessel:	n/a
44	chr8:6876781-6876831	BJ	skin:	n/a
45	chr8:6827800-6827850	PANC-1	pancreas:	n/a
46	chr8:6873754-6873804	HCF	heart:	n/a
47	chr8:6828103-6828153	PFSK-1	brain:	n/a
48	chr8:6827814-6827864	BJ	skin:	n/a
49	chr8:6873754-6873804	SAEC	small airway:	n/a
50	chr8:6827800-6827850	T-47D	breast:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:6813895..6816114-chr8:6818168..6820677,2	MCF-7	breast:
2	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-DEFA1B-1	chr8:6847181-6847243	NONHSAT124804
3	lnc-DEFA1-1	chr8:6826461-6826635	NONHSAT124803
4	lnc-DEFA1-1	chr8:6825663-6825775	NONHSAT124803
5	lnc-DEFA1B-1	chr8:6845622-6845808	NONHSAT124804
6	lnc-DEFA1B-1	chr8:6844700-6844945	NONHSAT124804
7	lnc-DEFA1-1	chr8:6825663-6825769	NONHSAT124802

No data

Variant related genes	Relation type
DEFA9P	TF binding region
DEFA3	TF binding region
DEFT1P	TF binding region
DEFA1B	TF binding region
DEFT1P2	TF binding region
DEFA10P	TF binding region
DEFA1	TF binding region
DEFA9P	CpG island
DEFA3	CpG island
DEFT1P	CpG island
DEFA1B	CpG island
DEFT1P2	CpG island
DEFA10P	CpG island
DEFA1	CpG island

Extended variants
information (count: 1692 )
Associated
traits (count: 142 )

Variant overlapped rSNPs/rCNVs (count:1692 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs550860977	chr8:6818616-6818617	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs73661314	chr8:6818644-6818645	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs530281050	chr8:6818651-6818652	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs35867329	chr8:6818677-6818678	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs565463876	chr8:6818694-6818695	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs546896507	chr8:6818698-6818699	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs566862571	chr8:6818699-6818700	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs538642093	chr8:6818737-6818738	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs558558776	chr8:6818738-6818739	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs569239071	chr8:6818760-6818761	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs187416219	chr8:6818767-6818768	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs2738067	chr8:6818775-6818776	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs573782662	chr8:6818803-6818804	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs530769398	chr8:6818808-6818809	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs200119420	chr8:6818809-6818810	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs190368371	chr8:6818819-6818820	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs553295966	chr8:6818862-6818863	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs573222381	chr8:6818872-6818873	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs544373289	chr8:6818909-6818910	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs77121997	chr8:6818964-6818965	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs564910732	chr8:6819056-6819057	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs530494618	chr8:6819066-6819067	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs146573190	chr8:6819071-6819072	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs5889193	chr8:6819072-6819073	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs75114569	chr8:6819080-6819081	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs398007003	chr8:6819081-6819082	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs544298091	chr8:6819103-6819104	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs561281778	chr8:6819114-6819115	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs183973225	chr8:6819122-6819123	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs556598198	chr8:6819155-6819156	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs566805026	chr8:6819161-6819162	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs141568748	chr8:6819190-6819191	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs561350783	chr8:6819217-6819218	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs62488525	chr8:6819244-6819245	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs189170195	chr8:6819268-6819269	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs537906246	chr8:6819313-6819314	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs548672025	chr8:6819327-6819328	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs57870918	chr8:6819344-6819345	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs536447950	chr8:6819346-6819347	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs553236915	chr8:6819356-6819357	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs573138814	chr8:6819361-6819362	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs193082924	chr8:6819367-6819368	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs111501297	chr8:6819370-6819371	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs6991057	chr8:6819384-6819385	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs2702853	chr8:6819391-6819392	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs543909213	chr8:6819406-6819407	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs561033193	chr8:6819430-6819431	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs368461776	chr8:6819431-6819432	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs540413245	chr8:6819434-6819435	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs184667680	chr8:6819438-6819439	Weak transcription	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:47 , 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	chr8:6817400-6818800	Enhancers	Primary neutrophils fromperipheralblood	blood
3	chr8:6817800-6820600	Weak transcription	Fetal Thymus	thymus
4	chr8:6818000-6820400	Weak transcription	Dnd41	blood
5	chr8:6818800-6822800	Weak transcription	Primary neutrophils fromperipheralblood	blood
6	chr8:6820400-6821800	Enhancers	Dnd41	blood
7	chr8:6820600-6821600	Enhancers	Fetal Thymus	thymus
8	chr8:6821400-6821800	Enhancers	Thymus	Thymus
9	chr8:6822800-6830000	Enhancers	Primary neutrophils fromperipheralblood	blood
10	chr8:6824000-6824800	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
11	chr8:6824200-6824600	Enhancers	H1 Cell Line	embryonic stem cell
12	chr8:6824400-6824800	Bivalent Enhancer	Monocytes-CD14+_RO01746	blood
13	chr8:6824600-6824800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr8:6824600-6828200	Weak transcription	H1 Cell Line	embryonic stem cell
15	chr8:6824800-6829200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr8:6826400-6826600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
17	chr8:6826400-6826800	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
18	chr8:6826400-6826800	Enhancers	Primary T cells fromperipheralblood	blood
19	chr8:6826400-6826800	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
20	chr8:6826400-6826800	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr8:6826400-6827000	Bivalent Enhancer	Primary B cells from peripheral blood	blood
22	chr8:6826600-6826800	Bivalent Enhancer	Monocytes-CD14+_RO01746	blood
23	chr8:6828200-6828600	Enhancers	H1 Cell Line	embryonic stem cell
24	chr8:6828200-6828600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
25	chr8:6828400-6828600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
26	chr8:6828600-6829600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
27	chr8:6829200-6829400	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr8:6829200-6829400	Enhancers	Right Ventricle	heart
29	chr8:6829200-6830200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr8:6829600-6830000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
31	chr8:6829600-6830000	Enhancers	Fetal Brain Male	brain
32	chr8:6829600-6830200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
33	chr8:6829800-6830000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr8:6830000-6833000	Weak transcription	Primary neutrophils fromperipheralblood	blood
35	chr8:6831000-6831200	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
36	chr8:6833000-6833600	Enhancers	Primary neutrophils fromperipheralblood	blood
37	chr8:6833600-6837800	Weak transcription	Primary neutrophils fromperipheralblood	blood
38	chr8:6837800-6838200	Enhancers	Primary neutrophils fromperipheralblood	blood
39	chr8:6838200-6840600	Weak transcription	Primary neutrophils fromperipheralblood	blood
40	chr8:6840600-6841800	Enhancers	Primary neutrophils fromperipheralblood	blood
41	chr8:6856800-6857400	Enhancers	Primary neutrophils fromperipheralblood	blood
42	chr8:6863200-6866800	Weak transcription	Primary neutrophils fromperipheralblood	blood
43	chr8:6867000-6871800	Weak transcription	Primary neutrophils fromperipheralblood	blood
44	chr8:6871800-6873000	Enhancers	Primary neutrophils fromperipheralblood	blood
45	chr8:6872400-6872600	Enhancers	Primary hematopoietic stem cells	blood
46	chr8:6873000-6873400	Weak transcription	Primary neutrophils fromperipheralblood	blood
47	chr8:6873400-6884600	Enhancers	Primary neutrophils fromperipheralblood	blood

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