Variant report

Variant	nsv971710
Chromosome Location	chr8:11867184-11883657
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:11872669-11872691	HepG2	liver:	n/a	n/a
2	CCNT2	chr8:11872580-11872794	K562	blood:	n/a	n/a
3	CTCF	chr8:11872660-11872810	HFF	foreskin:	n/a	chr8:11872722-11872738 chr8:11872721-11872739
4	CTCF	chr8:11872606-11872874	K562	blood:	n/a	chr8:11872722-11872738 chr8:11872721-11872739
5	CTCF	chr8:11872613-11872858	Pancreas_OC	pancreas:	n/a	chr8:11872722-11872738 chr8:11872721-11872739
6	CTCF	chr8:11872640-11872790	GM12875	blood:	n/a	chr8:11872722-11872738 chr8:11872721-11872739
7	CTCF	chr8:11872611-11872879	MCF-7	breast:	n/a	chr8:11872722-11872738 chr8:11872721-11872739
8	CTCF	chr8:11872640-11872790	HRE	kidney:	n/a	chr8:11872722-11872738 chr8:11872721-11872739
9	CTCF	chr8:11872589-11872936	GM12891	blood:	n/a	chr8:11872722-11872738 chr8:11872721-11872739
10	CTCF	chr8:11872592-11872899	H1-hESC	embryonic stem cell:	n/a	chr8:11872722-11872738 chr8:11872721-11872739
11	CTCF	chr8:11872623-11872861	Kidney_OC	kidney:	n/a	chr8:11872722-11872738 chr8:11872721-11872739
12	CTCF	chr8:11872618-11872868	GM13977	blood:	n/a	chr8:11872722-11872738 chr8:11872721-11872739
13	CTCF	chr8:11872583-11872907	GM12892	blood:	n/a	chr8:11872722-11872738 chr8:11872721-11872739
14	CTCF	chr8:11872640-11872790	GM12868	blood:	n/a	chr8:11872722-11872738 chr8:11872721-11872739
15	CTCF	chr8:11872680-11872830	SK-N-SH_RA	brain:	n/a	chr8:11872722-11872738 chr8:11872721-11872739
16	CTCF	chr8:11872780-11872930	HAc	cerebellar:	n/a	n/a
17	CTCF	chr8:11872680-11872830	HepG2	liver:	n/a	chr8:11872722-11872738 chr8:11872721-11872739
18	CTCF	chr8:11872660-11872810	HRPEpiC	eye:	n/a	chr8:11872722-11872738 chr8:11872721-11872739
19	CTCF	chr8:11872640-11872790	GM12865	blood:	n/a	chr8:11872722-11872738 chr8:11872721-11872739
20	CTCF	chr8:11872640-11872790	HCM	heart:	n/a	chr8:11872722-11872738 chr8:11872721-11872739
21	CTCF	chr8:11872640-11872790	GM12872	blood:	n/a	chr8:11872722-11872738 chr8:11872721-11872739
22	CTCF	chr8:11872740-11872890	K562	blood:	n/a	n/a
23	CTCF	chr8:11872640-11872790	AoAF	blood vessel:	n/a	chr8:11872722-11872738 chr8:11872721-11872739
24	CTCF	chr8:11872555-11872921	A549	lung:	n/a	chr8:11872722-11872738 chr8:11872721-11872739
25	CTCF	chr8:11872540-11872810	GM12866	blood:	n/a	chr8:11872722-11872738 chr8:11872721-11872739
26	CTCF	chr8:11873260-11873410	GM12875	blood:	n/a	n/a
27	CTCF	chr8:11872640-11872790	HVMF	connective:	n/a	chr8:11872722-11872738 chr8:11872721-11872739
28	CTCF	chr8:11872640-11872790	AG04450	lung:	n/a	chr8:11872722-11872738 chr8:11872721-11872739
29	CTCF	chr8:11872840-11872990	HMEC	breast:	n/a	n/a
30	CTCF	chr8:11872619-11872786	SK-N-SH_RA	brain:	n/a	chr8:11872722-11872738 chr8:11872721-11872739
31	CTCF	chr8:11872596-11872850	GM13976	blood:	n/a	chr8:11872722-11872738 chr8:11872721-11872739
32	CTCF	chr8:11872760-11872910	HPF	lung:	n/a	n/a
33	CTCF	chr8:11872645-11872849	MCF-7	breast:	n/a	chr8:11872722-11872738 chr8:11872721-11872739
34	CTCF	chr8:11872660-11872810	MCF-7	breast:	n/a	chr8:11872722-11872738 chr8:11872721-11872739
35	CTCF	chr8:11872660-11872810	HVMF	connective:	n/a	chr8:11872722-11872738 chr8:11872721-11872739
36	CTCF	chr8:11872609-11872888	A549	lung:	n/a	chr8:11872722-11872738 chr8:11872721-11872739
37	CTCF	chr8:11872660-11872810	NHDF-neo	bronchial:	n/a	chr8:11872722-11872738 chr8:11872721-11872739
38	CTCF	chr8:11872640-11872790	HEEpiC	esophagus:	n/a	chr8:11872722-11872738 chr8:11872721-11872739
39	CTCF	chr8:11872595-11872884	GM10248	blood:	n/a	chr8:11872722-11872738 chr8:11872721-11872739
40	CTCF	chr8:11872680-11872830	GM12872	blood:	n/a	chr8:11872722-11872738 chr8:11872721-11872739
41	CTCF	chr8:11872593-11872901	GM19238	blood:	n/a	chr8:11872722-11872738 chr8:11872721-11872739
42	CTCF	chr8:11872563-11872926	K562	blood:	n/a	chr8:11872722-11872738 chr8:11872721-11872739
43	CTCF	chr8:11872585-11872957	MCF-7	breast:	n/a	chr8:11872722-11872738 chr8:11872721-11872739
44	CTCF	chr8:11872658-11872826	HepG2	liver:	n/a	chr8:11872722-11872738 chr8:11872721-11872739
45	CTCF	chr8:11872507-11873004	K562	blood:	n/a	chr8:11872722-11872738 chr8:11872721-11872739
46	CTCF	chr8:11872640-11872790	SAEC	small airway:	n/a	chr8:11872722-11872738 chr8:11872721-11872739
47	CTCF	chr8:11872613-11872884	GM19239	blood:	n/a	chr8:11872722-11872738 chr8:11872721-11872739
48	CTCF	chr8:11873280-11873430	HCPEpiC	choroid plexus:	n/a	n/a
49	CTCF	chr8:11872640-11872790	AG09319	gingival:	n/a	chr8:11872722-11872738 chr8:11872721-11872739
50	CTCF	chr8:11872660-11872810	GM12866	blood:	n/a	chr8:11872722-11872738 chr8:11872721-11872739

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:11872141-11872191	Hela-S3	cervix:	n/a
2	chr8:11872778-11872828	NHBE	bronchial:	n/a
3	chr8:11882897-11882947	NHBE	bronchial:	n/a
4	chr8:11882897-11882947	HCPEpiC	choroid plexus:	n/a
5	chr8:11876646-11876696	T-47D	breast:	n/a
6	chr8:11870338-11870388	AG09319	gingival:	n/a
7	chr8:11872882-11872932	NT2-D1	testis:	n/a
8	chr8:11872882-11872932	AG04449	skin:	fetal
9	chr8:11872778-11872828	Hepatocyte	liver:	n/a
10	chr8:11872882-11872932	HepG2	liver:	n/a
11	chr8:11872659-11872709	GM12892	blood:	n/a
12	chr8:11872778-11872828	SK-N-MC	brain:	n/a
13	chr8:11870338-11870388	Caco-2	colon:	n/a
14	chr8:11872882-11872932	K562	blood:	n/a
15	chr8:11876646-11876696	NH-A	brain:	n/a
16	chr8:11882982-11883032	MCF10A-Er-Src	breast:	n/a
17	chr8:11870063-11870113	PrEC	prostate:	n/a
18	chr8:11872659-11872709	NB4	blood:	n/a
19	chr8:11870063-11870113	SK-N-SH	brain:	n/a
20	chr8:11882982-11883032	RPTEC	kidney:	n/a
21	chr8:11872659-11872709	ProgFib	skin:	n/a
22	chr8:11882962-11883012	ovcar-3	ovarian:	n/a
23	chr8:11872141-11872191	AG10803	skin:	n/a
24	chr8:11872141-11872191	HCF	heart:	n/a
25	chr8:11872141-11872191	HEEpiC	esophagus:	n/a
26	chr8:11872659-11872709	HEEpiC	esophagus:	n/a
27	chr8:11882897-11882947	GM19239	blood:	n/a
28	chr8:11882962-11883012	Caco-2	colon:	n/a
29	chr8:11882982-11883032	K562	blood:	n/a
30	chr8:11872659-11872709	HUVEC	blood vessel:	n/a
31	chr8:11872778-11872828	HAEpiC	amniotic membrane:	n/a
32	chr8:11882897-11882947	SK-N-SH	brain:	n/a
33	chr8:11882982-11883032	NB4	blood:	n/a
34	chr8:11872141-11872191	NHBE	bronchial:	n/a
35	chr8:11882897-11882947	HCT-116	colon:	n/a
36	chr8:11872659-11872709	ECC-1	luminal epithelium:	n/a
37	chr8:11882897-11882947	NH-A	brain:	n/a
38	chr8:11872778-11872828	NH-A	brain:	n/a
39	chr8:11872141-11872191	H1-hESC	embryonic stem cell:	embryo
40	chr8:11872778-11872828	CMK	blood:	n/a
41	chr8:11882982-11883032	Caco-2	colon:	n/a
42	chr8:11870338-11870388	ProgFib	skin:	n/a
43	chr8:11882962-11883012	HL-60	blood:	n/a
44	chr8:11882962-11883012	HCM	heart:	n/a
45	chr8:11872141-11872191	MCF-7	breast:	n/a
46	chr8:11872141-11872191	AoSMC	blood vessel:	n/a
47	chr8:11872778-11872828	HNPCEpiC	eye:	n/a
48	chr8:11872659-11872709	BE2_C	brain:	n/a
49	chr8:11882897-11882947	HEEpiC	esophagus:	n/a
50	chr8:11870063-11870113	HEK293	kidney:	embryo

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:11819737..11820672-chr8:11872272..11872975,3	MCF-7	breast:
2	chr11:64863606..64864139-chr8:11882400..11882963,2	Hela-S3	cervix:

Variant related genes	Relation type
ENSG00000255016	TF binding region
ENSG00000255098	TF binding region
ENSG00000255016	CpG island
ENSG00000255098	CpG island
ENSG00000149823	chromatin interactions

Extended variants
information (count: 852 )
Associated
traits (count: 140 )

Variant overlapped rSNPs/rCNVs (count:852 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs555485562	chr8:11867202-11867203	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs143013861	chr8:11867206-11867207	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs546694849	chr8:11867223-11867224	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs55798133	chr8:11867248-11867249	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs55805862	chr8:11867252-11867253	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs535302408	chr8:11867256-11867257	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs139058606	chr8:11867264-11867265	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs575473040	chr8:11867273-11867274	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs111989634	chr8:11867281-11867282	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs192643562	chr8:11867284-11867285	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs377619741	chr8:11867289-11867290	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs370720455	chr8:11867308-11867309	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs35023291	chr8:11867312-11867313	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs114577679	chr8:11867375-11867376	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs568857832	chr8:11867379-11867380	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs184623893	chr8:11867396-11867397	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs141620923	chr8:11867402-11867403	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs529486885	chr8:11867418-11867419	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs551216389	chr8:11867470-11867471	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs150544206	chr8:11867500-11867501	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs117672255	chr8:11867580-11867581	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs551704604	chr8:11867584-11867585	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs116312355	chr8:11867596-11867597	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs111401888	chr8:11867598-11867599	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs534236403	chr8:11867602-11867603	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs139515133	chr8:11867607-11867608	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs149730354	chr8:11867631-11867632	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs533700879	chr8:11867648-11867649	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs369964207	chr8:11867655-11867656	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs535247202	chr8:11867676-11867677	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs113424588	chr8:11867679-11867680	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs574922617	chr8:11867704-11867705	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs367946699	chr8:11867706-11867707	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs575458884	chr8:11867707-11867708	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs539355800	chr8:11867709-11867710	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs374242621	chr8:11867716-11867717	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs558079983	chr8:11867721-11867722	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs572742830	chr8:11867730-11867731	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs202225083	chr8:11867749-11867750	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs540266632	chr8:11867789-11867790	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs147394547	chr8:11867790-11867791	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs573794396	chr8:11867805-11867806	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs544776313	chr8:11867811-11867812	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs562944013	chr8:11867818-11867819	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs533619651	chr8:11867850-11867851	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs573294365	chr8:11867863-11867864	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs112473793	chr8:11867870-11867871	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs560873467	chr8:11867897-11867898	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs527665265	chr8:11867901-11867902	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs548989294	chr8:11867934-11867935	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:140)

Disease	PMID	Source
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
Acute myeloid leukemia	21251322	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
Lung squamous cell carcinoma	22363434	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
Myxofibrosarcoma	16751306	CNVD
Immune disease	21572526	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Kallmann Syndrome 2	22470819	CNVD
Developmental disorder	20461109	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Glioblastoma multiforme	21138945	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Gastric cancer	21811585	CNVD
Colorectal cancer	16774939	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Cancer	20164919	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD
Renal cell carcinoma	21215367	CNVD

Chromatin state (count:222 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:11866800-11867200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr8:11867000-11867200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr8:11867000-11867400	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr8:11867000-11869800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
5	chr8:11867200-11868000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr8:11868000-11869800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr8:11869000-11869200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr8:11869800-11870200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr8:11869800-11870400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
10	chr8:11870200-11871000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr8:11870400-11872800	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
12	chr8:11870800-11871200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr8:11871000-11871200	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr8:11871200-11872800	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr8:11871400-11871600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr8:11871400-11871800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr8:11871400-11872600	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
18	chr8:11871600-11871800	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr8:11871600-11871800	Enhancers	Breast Myoepithelial Primary Cells	Breast
20	chr8:11871600-11871800	Enhancers	Stomach Smooth Muscle	stomach
21	chr8:11871600-11872000	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
22	chr8:11871600-11872000	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
23	chr8:11871600-11872000	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
24	chr8:11871600-11872000	Bivalent Enhancer	Fetal Stomach	stomach
25	chr8:11871600-11872000	Enhancers	HMEC	breast
26	chr8:11871800-11872000	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
27	chr8:11871800-11872200	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
28	chr8:11871800-11872200	Enhancers	Colon Smooth Muscle	Colon
29	chr8:11871800-11872400	Enhancers	Primary B cells from cord blood	blood
30	chr8:11871800-11872400	Bivalent Enhancer	Primary B cells from peripheral blood	blood
31	chr8:11871800-11872400	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
32	chr8:11871800-11872600	Active TSS	H9 Cell Line	embryonic stem cell
33	chr8:11871800-11872600	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
34	chr8:11871800-11872600	Flanking Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
35	chr8:11871800-11872600	Active TSS	Breast Myoepithelial Primary Cells	Breast
36	chr8:11871800-11872600	Active TSS	Brain Anterior Caudate	brain
37	chr8:11871800-11872600	Active TSS	Stomach Smooth Muscle	stomach
38	chr8:11871800-11872800	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
39	chr8:11871800-11873000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
40	chr8:11872000-11872200	Bivalent/Poised TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
41	chr8:11872000-11872200	Flanking Bivalent TSS/Enh	ES-UCSF4 Cell Line	embryonic stem cell
42	chr8:11872000-11872200	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
43	chr8:11872000-11872200	Enhancers	Primary hematopoietic stem cells	blood
44	chr8:11872000-11872200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
45	chr8:11872000-11872200	Bivalent/Poised TSS	Primary T regulatory cells fromperipheralblood	blood
46	chr8:11872000-11872200	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
47	chr8:11872000-11872200	Flanking Bivalent TSS/Enh	Foreskin Keratinocyte Primary Cells skin03	Skin
48	chr8:11872000-11872200	Flanking Active TSS	Adipose Nuclei	Adipose
49	chr8:11872000-11872200	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
50	chr8:11872000-11872200	Enhancers	Fetal Brain Male	brain

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