Variant report

Variant	nsv1028783
Chromosome Location	chr8:132261833-132345698
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:211)
CpG islands
(count:183)
Chromatin interactive
region (count:2)
LncRNA
region (count:20)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:211 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr8:132262389-132262714	GM12878	blood:	n/a	n/a
2	ATF2	chr8:132262328-132262736	GM12878	blood:	n/a	n/a
3	BATF	chr8:132262385-132262656	GM12878	blood:	n/a	n/a
4	BATF	chr8:132262405-132262881	GM12878	blood:	n/a	n/a
5	BCL11A	chr8:132262386-132262712	GM12878	blood:	n/a	n/a
6	BHLHE40	chr8:132262465-132262624	GM12878	blood:	n/a	n/a
7	BHLHE40	chr8:132291607-132291897	HepG2	liver:	n/a	n/a
8	CEBPB	chr8:132308001-132308313	A549	lung:	n/a	chr8:132308136-132308147
9	CEBPB	chr8:132308016-132308282	IMR90	lung:	n/a	chr8:132308136-132308147
10	CEBPB	chr8:132287688-132287964	A549	lung:	n/a	chr8:132287801-132287812
11	CEBPB	chr8:132300921-132301202	A549	lung:	n/a	n/a
12	CEBPB	chr8:132308012-132308313	HepG2	liver:	n/a	chr8:132308136-132308147
13	CEBPB	chr8:132287674-132287908	IMR90	lung:	n/a	chr8:132287801-132287812
14	CEBPB	chr8:132308078-132308278	K562	blood:	n/a	chr8:132308136-132308147
15	CEBPB	chr8:132262246-132262769	HCT-116	colon:	n/a	n/a
16	CEBPB	chr8:132262126-132262722	HCT-116	colon:	n/a	n/a
17	CEBPB	chr8:132287668-132287976	HepG2	liver:	n/a	chr8:132287801-132287812
18	CEBPB	chr8:132312981-132313310	H1-hESC	embryonic stem cell:	n/a	n/a
19	CHD2	chr8:132330146-132330241	H1-hESC	embryonic stem cell:	n/a	n/a
20	CTCF	chr8:132323352-132323437	GM13976	blood:	n/a	n/a
21	CTCF	chr8:132312532-132312569	Fibrobl	skin:	n/a	n/a
22	CTCF	chr8:132271709-132271780	Lung_OC	lung:	n/a	n/a
23	CTCF	chr8:132275403-132275423	Lung_OC	lung:	n/a	n/a
24	E2F4	chr8:132287450-132287805	MCF10A-Er-Src	breast:	n/a	n/a
25	E2F4	chr8:132307589-132307772	MCF10A-Er-Src	breast:	n/a	n/a
26	E2F4	chr8:132268767-132268967	MCF10A-Er-Src	breast:	n/a	n/a
27	E2F4	chr8:132300971-132301271	MCF10A-Er-Src	breast:	n/a	n/a
28	E2F4	chr8:132262376-132262598	MCF10A-Er-Src	breast:	n/a	n/a
29	E2F4	chr8:132318964-132319081	MCF10A-Er-Src	breast:	n/a	n/a
30	EBF1	chr8:132262418-132262596	GM12878	blood:	n/a	n/a
31	EBF1	chr8:132262586-132262898	GM12878	blood:	n/a	n/a
32	EP300	chr8:132301423-132302438	SK-N-SH	brain:	n/a	n/a
33	EP300	chr8:132262543-132262585	GM12878	blood:	n/a	n/a
34	EP300	chr8:132301990-132302239	SK-N-SH_RA	brain:	n/a	n/a
35	EP300	chr8:132262393-132262673	GM12878	blood:	n/a	n/a
36	EP300	chr8:132301945-132302189	SK-N-SH_RA	brain:	n/a	n/a
37	FOS	chr8:132262292-132262692	MCF10A-Er-Src	breast:	n/a	n/a
38	FOS	chr8:132300791-132301575	MCF10A-Er-Src	breast:	n/a	n/a
39	FOS	chr8:132307668-132307833	MCF10A-Er-Src	breast:	n/a	n/a
40	FOS	chr8:132296893-132297033	MCF10A-Er-Src	breast:	n/a	chr8:132296982-132296990
41	FOS	chr8:132262183-132262756	MCF10A-Er-Src	breast:	n/a	n/a
42	FOS	chr8:132300497-132301527	MCF10A-Er-Src	breast:	n/a	n/a
43	FOS	chr8:132296946-132297121	MCF10A-Er-Src	breast:	n/a	chr8:132296982-132296990
44	FOS	chr8:132308809-132309036	MCF10A-Er-Src	breast:	n/a	n/a
45	FOS	chr8:132300648-132301517	MCF10A-Er-Src	breast:	n/a	n/a
46	FOS	chr8:132262312-132262725	MCF10A-Er-Src	breast:	n/a	n/a
47	FOS	chr8:132307668-132308009	MCF10A-Er-Src	breast:	n/a	n/a
48	FOS	chr8:132296904-132297095	MCF10A-Er-Src	breast:	n/a	chr8:132296982-132296990
49	FOS	chr8:132261889-132262745	MCF10A-Er-Src	breast:	n/a	n/a
50	FOS	chr8:132300861-132301363	MCF10A-Er-Src	breast:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:132313141-132313191	Caco-2	colon:	n/a
2	chr8:132329846-132329896	U87	brain:	n/a
3	chr8:132321917-132321967	K562	blood:	n/a
4	chr8:132321917-132321967	HMEC	breast:	n/a
5	chr8:132313141-132313191	NHDF-neo	bronchial:	n/a
6	chr8:132321917-132321967	SAEC	small airway:	n/a
7	chr8:132313141-132313191	IMR90	lung:	fetal
8	chr8:132329846-132329896	HNPCEpiC	eye:	n/a
9	chr8:132321917-132321967	AG10803	skin:	n/a
10	chr8:132321917-132321967	Jurkat	blood:	n/a
11	chr8:132329846-132329896	GM12892	blood:	n/a
12	chr8:132329846-132329896	HEK293	kidney:	embryo
13	chr8:132313141-132313191	AG09309	skin:	n/a
14	chr8:132313141-132313191	CMK	blood:	n/a
15	chr8:132329846-132329896	NB4	blood:	n/a
16	chr8:132329846-132329896	CMK	blood:	n/a
17	chr8:132329846-132329896	HL-60	blood:	n/a
18	chr8:132313141-132313191	H1-hESC	embryonic stem cell:	embryo
19	chr8:132313141-132313191	Hepatocyte	liver:	n/a
20	chr8:132313141-132313191	MCF10A-Er-Src	breast:	n/a
21	chr8:132321917-132321967	HCF	heart:	n/a
22	chr8:132321917-132321967	AG09319	gingival:	n/a
23	chr8:132321917-132321967	SKMC	muscle:	n/a
24	chr8:132313141-132313191	HEK293	kidney:	embryo
25	chr8:132313141-132313191	NB4	blood:	n/a
26	chr8:132329846-132329896	BE2_C	brain:	n/a
27	chr8:132313141-132313191	SK-N-MC	brain:	n/a
28	chr8:132313141-132313191	ovcar-3	ovarian:	n/a
29	chr8:132329846-132329896	T-47D	breast:	n/a
30	chr8:132329846-132329896	HCPEpiC	choroid plexus:	n/a
31	chr8:132329846-132329896	AG04449	skin:	fetal
32	chr8:132321917-132321967	HRPEpiC	eye:	n/a
33	chr8:132313141-132313191	HEEpiC	esophagus:	n/a
34	chr8:132329846-132329896	SAEC	small airway:	n/a
35	chr8:132329846-132329896	PANC-1	pancreas:	n/a
36	chr8:132313141-132313191	GM12891	blood:	n/a
37	chr8:132313141-132313191	SK-N-SH	brain:	n/a
38	chr8:132313141-132313191	Jurkat	blood:	n/a
39	chr8:132321917-132321967	NB4	blood:	n/a
40	chr8:132321917-132321967	PrEC	prostate:	n/a
41	chr8:132321917-132321967	HNPCEpiC	eye:	n/a
42	chr8:132313141-132313191	AG04449	skin:	fetal
43	chr8:132329846-132329896	MCF-7	breast:	n/a
44	chr8:132321917-132321967	LNCaP	prostate:	n/a
45	chr8:132321917-132321967	H1-hESC	embryonic stem cell:	embryo
46	chr8:132329846-132329896	NHDF-neo	bronchial:	n/a
47	chr8:132313141-132313191	HRCEpiC	kidney:	n/a
48	chr8:132313141-132313191	NH-A	brain:	n/a
49	chr8:132321917-132321967	ProgFib	skin:	n/a
50	chr8:132313141-132313191	HMEC	breast:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:132340219..132342032-chr8:132342254..132344469,2	K562	blood:
2	chr8:132340219..132342032-chr8:132342254..132344469,2	K562	blood:

(count:20 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-EFR3A-1	chr8:132320792-132320918	ENSG00000253507
2	lnc-EFR3A-1	chr8:132329581-132329830	ENSG00000253507
3	lnc-EFR3A-1	chr8:132324624-132325013	NONHSAT129174
4	lnc-EFR3A-1	chr8:132322800-132322959	ENSG00000253507
5	lnc-EFR3A-1	chr8:132329581-132329879	ENSG00000253507
6	lnc-EFR3A-1	chr8:132329581-132329753	ENSG00000253507
7	lnc-EFR3A-1	chr8:132324803-132324995	ENSG00000253507
8	lnc-EFR3A-1	chr8:132320792-132320918	ENSG00000253507
9	lnc-EFR3A-1	chr8:132328007-132328130	ENSG00000253507
10	lnc-EFR3A-1	chr8:132322719-132322959	ENSG00000253507
11	lnc-EFR3A-1	chr8:132328007-132328130	ENSG00000253507
12	lnc-EFR3A-1	chr8:132320762-132320918	NONHSAT129170
13	lnc-EFR3A-1	chr8:132324803-132324995	ENSG00000253507
14	lnc-EFR3A-1	chr8:132322800-132322959	ENSG00000253507
15	lnc-EFR3A-1	chr8:132327084-132327225	NONHSAT129174
16	lnc-EFR3A-1	chr8:132324803-132324976	ENSG00000253507
17	lnc-EFR3A-1	chr8:132328007-132328130	ENSG00000253507
18	lnc-EFR3A-1	chr8:132322800-132323052	NONHSAT129170
19	lnc-EFR3A-1	chr8:132329581-132330809	NONHSAT129174
20	lnc-EFR3A-1	chr8:132327256-132328130	NONHSAT129174

No data

Variant related genes	Relation type
ENSG00000253507	TF binding region
ENSG00000253507	CpG island

Extended variants
information (count: 2532 )
Associated
traits (count: 138 )

Variant overlapped rSNPs/rCNVs (count:2532 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs377439273	chr8:132262013-132262014	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs550817358	chr8:132262039-132262040	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs554309951	chr8:132262049-132262050	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs143778035	chr8:132262083-132262084	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs548544843	chr8:132262122-132262123	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs572831727	chr8:132262131-132262132	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs570574846	chr8:132262168-132262169	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs186953007	chr8:132262170-132262171	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs571668469	chr8:132262171-132262172	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs566897044	chr8:132262203-132262204	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs191786517	chr8:132262214-132262215	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs369266533	chr8:132262223-132262224	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs373444013	chr8:132262242-132262243	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs550773062	chr8:132262243-132262244	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs140582758	chr8:132262263-132262264	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs182015927	chr8:132262264-132262265	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs572399483	chr8:132262271-132262272	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs145644744	chr8:132262280-132262281	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs73343753	chr8:132262281-132262282	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs186510253	chr8:132262282-132262283	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs374860003	chr8:132262293-132262294	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs558498736	chr8:132262322-132262323	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs140719855	chr8:132262336-132262337	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs564915382	chr8:132262367-132262368	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs190863965	chr8:132262393-132262394	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs201957152	chr8:132262400-132262401	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs71276525	chr8:132262462-132262463	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs117680693	chr8:132262485-132262486	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs145149433	chr8:132262490-132262491	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs574734087	chr8:132262503-132262504	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs182299785	chr8:132262508-132262509	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs560468609	chr8:132262532-132262533	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs576285078	chr8:132262541-132262542	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs149138050	chr8:132262545-132262546	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs546696112	chr8:132262547-132262548	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs539596935	chr8:132262567-132262568	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs200011102	chr8:132262581-132262582	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs546721422	chr8:132262593-132262594	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs562667574	chr8:132262631-132262632	ZNF genes & repeats Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs143205922	chr8:132262654-132262655	ZNF genes & repeats Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs529856536	chr8:132262655-132262656	ZNF genes & repeats Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs12681982	chr8:132262703-132262704	ZNF genes & repeats Flanking Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs536450293	chr8:132262706-132262707	ZNF genes & repeats Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs187843888	chr8:132262743-132262744	ZNF genes & repeats Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs78161845	chr8:132262744-132262745	ZNF genes & repeats Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs191333999	chr8:132262754-132262755	ZNF genes & repeats Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs558971667	chr8:132262755-132262756	ZNF genes & repeats Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs576813761	chr8:132262769-132262770	ZNF genes & repeats Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs560010456	chr8:132262770-132262771	ZNF genes & repeats Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs183205130	chr8:132262775-132262776	ZNF genes & repeats Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:138)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Ewing''s sarcoma	21437220	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Gastric cancer	17908304	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Liver carcinoma	19366792	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Testicular cancer	18059402	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
abnormal development	18461090	CNVD
Oral cancer	21386901	CNVD
Uveal melanoma	21693616	CNVD
Langer-Giedion syndrome	22283845	CNVD
Cancer	21637783	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	20632083	CNVD
Breast cancer	17603634	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	19627613	CNVD
Prostate cancer	21088497	CNVD
colon cancer	17210682	CNVD
Breast cancer	21264507	CNVD
Breast cancer	22028636	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	16751803	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Gastric cancer	17167181	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	16461572	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
head and neck squamous cell carcinoma	18028549	CNVD
Breast cancer	17001317	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute myeloid leukemia	20729466	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	21399628	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	17393978	CNVD
Burkitt''s lymphoma	18698080	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Developmental delay	21147756	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Non-small cell lung cancer	19010865	CNVD
small cell lung cancer	20016488	CNVD
Papillary thyroid cancer	17515504	CNVD
Basal cell lymphoma	17053054	CNVD
Gastric cancer	21528007	CNVD
Breast cancer	22532251	CNVD
Cervical cancer	21062161	CNVD
Cancer	21129771	CNVD
benign familial neonatal convulsions	18472482	CNVD
Breast cancer	16417655	CNVD
Astrocytoma	17387387	CNVD
Cancer	21183584	CNVD
Follicular lymphoma	20505157	CNVD
T-cell lymphomas	19863542	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	20607354	CNVD
Breast cancer	20814816	CNVD
Colorectal cancer	22486879	CNVD
Breast cancer	17908964	CNVD
Colorectal cancer	20031965	CNVD
Hepatocellular carcinoma	16750200	CNVD
Ovarian cancer	17908964	CNVD
Ovarian cancer	20031965	CNVD
Prostate cancer	20031965	CNVD
Non-small cell lung cancer	17643093	CNVD
Prostate cancer	19242612	CNVD
Colorectal cancer	16774939	CNVD
Malignant melanoma	17260012	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Sezary syndrome	18413736	CNVD
Chordoma	18071362	CNVD
Breast cancer	17850661	CNVD
head and neck squamous cell carcinoma	16740747	CNVD
Gastric cancer	22539939	CNVD
Breast cancer	16272173	CNVD
Uveal melanoma	20484589	CNVD
Ovarian cancer	20844748	CNVD
Multiple myeloma	16616336	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21611746	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Colorectal cancer	21645411	CNVD
Glioblastoma multiforme	22286061	CNVD
Gastric cancer	16891809	CNVD
Colorectal cancer	19455253	CNVD
Pregnancies with abnormal ultrasound findings	21110858	CNVD
Breast cancer	19181860	CNVD
Brain cancer	19584924	CNVD
Medulloblastoma	19584924	CNVD
Follicular lymphoma	17699855	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:166 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:132262000-132262600	Enhancers	Primary monocytes fromperipheralblood	blood
2	chr8:132262000-132262800	Enhancers	HMEC	breast
3	chr8:132262200-132262600	Enhancers	GM12878-XiMat	blood
4	chr8:132262600-132262800	Flanking Active TSS	GM12878-XiMat	blood
5	chr8:132262600-132263400	ZNF genes & repeats	Primary monocytes fromperipheralblood	blood
6	chr8:132262800-132263000	Active TSS	GM12878-XiMat	blood
7	chr8:132272600-132274600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr8:132273600-132274600	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
9	chr8:132273600-132274800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
10	chr8:132281800-132282200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr8:132282200-132284000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr8:132284000-132284200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr8:132284200-132289200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr8:132289200-132290000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr8:132290000-132301800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr8:132290800-132292400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
17	chr8:132292400-132294800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
18	chr8:132294800-132295600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
19	chr8:132295600-132296800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
20	chr8:132297000-132297200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
21	chr8:132297000-132297600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr8:132297600-132300800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr8:132300600-132301200	Enhancers	HMEC	breast
24	chr8:132300800-132301000	Enhancers	Gastric	stomach
25	chr8:132300800-132301200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
26	chr8:132300800-132301200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr8:132300800-132301200	Enhancers	NH-A	brain
28	chr8:132300800-132302200	Enhancers	NHLF	lung
29	chr8:132300800-132303600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr8:132301200-132301400	Flanking Active TSS	NH-A	brain
31	chr8:132301200-132301600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr8:132301200-132301600	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr8:132301200-132301600	Flanking Active TSS	HMEC	breast
34	chr8:132301400-132301600	Enhancers	NH-A	brain
35	chr8:132301400-132302800	Enhancers	Pancreatic Islets	Pancreatic Islet
36	chr8:132301600-132301800	Flanking Active TSS	NH-A	brain
37	chr8:132301600-132302000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr8:132301600-132302400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr8:132301600-132303400	Enhancers	HMEC	breast
40	chr8:132301800-132302200	Enhancers	Fetal Intestine Large	intestine
41	chr8:132301800-132302200	Enhancers	NH-A	brain
42	chr8:132301800-132303200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
43	chr8:132301800-132303400	Enhancers	HUES6 Cell Line	embryonic stem cell
44	chr8:132301800-132304400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr8:132302400-132307600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr8:132302800-132303000	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
47	chr8:132302800-132303200	Enhancers	Fetal Brain Male	brain
48	chr8:132303000-132303200	Enhancers	Pancreatic Islets	Pancreatic Islet
49	chr8:132303000-132303600	Enhancers	Fetal Brain Female	brain
50	chr8:132303200-132303400	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet

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