Variant report

Variant	nsv982091
Chromosome Location	chr8:92203990-92240482
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	chr8:92219724-92220260	HepG2	liver:	n/a	n/a
2	BACH1	chr8:92229081-92229108	K562	blood:	n/a	n/a
3	BHLHE40	chr8:92232091-92232107	K562	blood:	n/a	n/a
4	BHLHE40	chr8:92220981-92221153	K562	blood:	n/a	n/a
5	CEBPB	chr8:92229097-92229306	K562	blood:	n/a	chr8:92229239-92229250
6	CEBPB	chr8:92219790-92220055	HepG2	liver:	n/a	chr8:92219938-92219947 chr8:92219936-92219947 chr8:92219936-92219949 chr8:92219938-92219947 chr8:92219938-92219947 chr8:92219938-92219947 chr8:92219936-92219949 chr8:92219938-92219949 chr8:92219921-92219932
7	CEBPB	chr8:92236328-92236620	IMR90	lung:	n/a	chr8:92236457-92236468
8	CEBPB	chr8:92219802-92220056	IMR90	lung:	n/a	chr8:92219938-92219947 chr8:92219936-92219947 chr8:92219936-92219949 chr8:92219938-92219947 chr8:92219938-92219947 chr8:92219938-92219947 chr8:92219936-92219949 chr8:92219938-92219949 chr8:92219921-92219932
9	CEBPB	chr8:92236330-92236543	MCF-7	breast:	n/a	chr8:92236457-92236468
10	CEBPB	chr8:92209832-92210032	K562	blood:	n/a	n/a
11	CEBPB	chr8:92236288-92236607	HepG2	liver:	n/a	chr8:92236457-92236468
12	CEBPB	chr8:92236330-92236617	K562	blood:	n/a	chr8:92236457-92236468
13	CEBPB	chr8:92236339-92236625	A549	lung:	n/a	chr8:92236457-92236468
14	CEBPB	chr8:92219542-92220264	MCF-7	breast:	n/a	chr8:92219938-92219947 chr8:92219936-92219947 chr8:92219936-92219949 chr8:92219938-92219947 chr8:92219938-92219947 chr8:92219938-92219947 chr8:92219936-92219949 chr8:92219938-92219949 chr8:92219921-92219932
15	CEBPB	chr8:92219759-92220129	A549	lung:	n/a	chr8:92219938-92219947 chr8:92219936-92219947 chr8:92219936-92219949 chr8:92219938-92219947 chr8:92219938-92219947 chr8:92219938-92219947 chr8:92219936-92219949 chr8:92219938-92219949 chr8:92219921-92219932
16	CEBPB	chr8:92229077-92229412	A549	lung:	n/a	chr8:92229239-92229250
17	CEBPB	chr8:92229081-92229410	HepG2	liver:	n/a	chr8:92229239-92229250
18	CEBPB	chr8:92219685-92220191	HepG2	liver:	n/a	chr8:92219938-92219947 chr8:92219936-92219947 chr8:92219936-92219949 chr8:92219938-92219947 chr8:92219938-92219947 chr8:92219938-92219947 chr8:92219936-92219949 chr8:92219938-92219949 chr8:92219921-92219932
19	CEBPB	chr8:92219688-92220245	MCF-7	breast:	n/a	chr8:92219938-92219947 chr8:92219936-92219947 chr8:92219936-92219949 chr8:92219938-92219947 chr8:92219938-92219947 chr8:92219938-92219947 chr8:92219936-92219949 chr8:92219938-92219949 chr8:92219921-92219932
20	CEBPB	chr8:92236328-92236573	K562	blood:	n/a	chr8:92236457-92236468
21	CEBPB	chr8:92219712-92220272	HepG2	liver:	n/a	chr8:92219938-92219947 chr8:92219936-92219947 chr8:92219936-92219949 chr8:92219938-92219947 chr8:92219938-92219947 chr8:92219938-92219947 chr8:92219936-92219949 chr8:92219938-92219949 chr8:92219921-92219932
22	CEBPB	chr8:92219743-92220226	HepG2	liver:	n/a	chr8:92219938-92219947 chr8:92219936-92219947 chr8:92219936-92219949 chr8:92219938-92219947 chr8:92219938-92219947 chr8:92219938-92219947 chr8:92219936-92219949 chr8:92219938-92219949 chr8:92219921-92219932
23	CEBPD	chr8:92219736-92220099	HepG2	liver:	n/a	chr8:92219938-92219947
24	CTCF	chr8:92211240-92211390	HMF	breast:	n/a	n/a
25	CTCF	chr8:92236168-92236209	Kidney_OC	kidney:	n/a	n/a
26	CTCF	chr8:92216254-92216291	GM10248	blood:	n/a	n/a
27	CTCF	chr8:92225300-92225450	BE2_C	brain:	n/a	n/a
28	CTCF	chr8:92225300-92225450	HPAF	blood vessel:	n/a	n/a
29	CTCF	chr8:92214185-92214227	LNCaP	prostate:	n/a	n/a
30	CUX1	chr8:92229185-92229191	K562	blood:	n/a	n/a
31	CUX1	chr8:92221844-92221880	K562	blood:	n/a	n/a
32	E2F4	chr8:92212060-92212222	MCF10A-Er-Src	breast:	n/a	n/a
33	EBF1	chr8:92216705-92217090	GM12878	blood:	n/a	chr8:92216887-92216898 chr8:92216889-92216898 chr8:92216889-92216898 chr8:92216888-92216898 chr8:92216887-92216900
34	EGR1	chr8:92209602-92209799	K562	blood:	n/a	n/a
35	EP300	chr8:92219730-92220303	HepG2	liver:	n/a	n/a
36	EP300	chr8:92219769-92220143	HepG2	liver:	n/a	n/a
37	EP300	chr8:92219798-92220323	HepG2	liver:	n/a	n/a
38	EP300	chr8:92239023-92239419	SK-N-SH_RA	brain:	n/a	n/a
39	EP300	chr8:92238854-92239725	SK-N-SH	brain:	n/a	chr8:92239565-92239579
40	EP300	chr8:92225088-92226274	SK-N-SH	brain:	n/a	chr8:92226003-92226013
41	EP300	chr8:92225332-92225733	SK-N-SH_RA	brain:	n/a	n/a
42	EP300	chr8:92238950-92239481	SK-N-SH_RA	brain:	n/a	n/a
43	EP300	chr8:92225289-92225775	SK-N-SH_RA	brain:	n/a	n/a
44	FAM48A	chr8:92224552-92224656	GM12878	blood:	n/a	n/a
45	FOXA1	chr8:92219806-92220049	T-47D	breast:	n/a	n/a
46	FOXA1	chr8:92219617-92220222	HepG2	liver:	n/a	n/a
47	FOXA1	chr8:92209376-92209768	HepG2	liver:	n/a	n/a
48	FOXA1	chr8:92219658-92220216	HepG2	liver:	n/a	n/a
49	FOXA1	chr8:92219651-92220190	HepG2	liver:	n/a	n/a
50	FOXA1	chr8:92219733-92220165	HepG2	liver:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:92220385-92220435	Caco-2	colon:	n/a
2	chr8:92220385-92220435	HepG2	liver:	n/a
3	chr8:92221717-92221767	HNPCEpiC	eye:	n/a
4	chr8:92220385-92220435	NT2-D1	testis:	n/a
5	chr8:92221717-92221767	Hepatocyte	liver:	n/a
6	chr8:92220385-92220435	SAEC	small airway:	n/a
7	chr8:92221717-92221767	GM06990	blood:	n/a
8	chr8:92221717-92221767	HUVEC	blood vessel:	n/a
9	chr8:92220385-92220435	BE2_C	brain:	n/a
10	chr8:92220385-92220435	HIPEpiC	eye:	n/a
11	chr8:92221717-92221767	NHDF-neo	bronchial:	n/a
12	chr8:92220385-92220435	Jurkat	blood:	n/a
13	chr8:92220385-92220435	HMEC	breast:	n/a
14	chr8:92221717-92221767	AG09309	skin:	n/a
15	chr8:92220385-92220435	HCM	heart:	n/a
16	chr8:92221717-92221767	MCF10A-Er-Src	breast:	n/a
17	chr8:92221717-92221767	HPAEpiC	pulmonary alveolar:	n/a
18	chr8:92221717-92221767	HEK293	kidney:	embryo
19	chr8:92221717-92221767	NHBE	bronchial:	n/a
20	chr8:92220385-92220435	AG10803	skin:	n/a
21	chr8:92221717-92221767	U87	brain:	n/a
22	chr8:92220385-92220435	K562	blood:	n/a
23	chr8:92221717-92221767	A549	lung:	n/a
24	chr8:92221717-92221767	BJ	skin:	n/a
25	chr8:92221717-92221767	Caco-2	colon:	n/a
26	chr8:92220385-92220435	SK-N-SH_RA	brain:	n/a
27	chr8:92221717-92221767	NB4	blood:	n/a
28	chr8:92220385-92220435	AG09319	gingival:	n/a
29	chr8:92221717-92221767	ProgFib	skin:	n/a
30	chr8:92221717-92221767	ECC-1	luminal epithelium:	n/a
31	chr8:92221717-92221767	SK-N-SH_RA	brain:	n/a
32	chr8:92221717-92221767	HCM	heart:	n/a
33	chr8:92220385-92220435	GM19239	blood:	n/a
34	chr8:92221717-92221767	Jurkat	blood:	n/a
35	chr8:92220385-92220435	AG04450	lung:	fetal
36	chr8:92221717-92221767	Hela-S3	cervix:	n/a
37	chr8:92221717-92221767	HepG2	liver:	n/a
38	chr8:92221717-92221767	IMR90	lung:	fetal
39	chr8:92221717-92221767	PANC-1	pancreas:	n/a
40	chr8:92220385-92220435	HRE	kidney:	n/a
41	chr8:92220385-92220435	HPAEpiC	pulmonary alveolar:	n/a
42	chr8:92221717-92221767	NT2-D1	testis:	n/a
43	chr8:92221717-92221767	K562	blood:	n/a
44	chr8:92221717-92221767	AG09319	gingival:	n/a
45	chr8:92220385-92220435	SK-N-SH	brain:	n/a
46	chr8:92220385-92220435	PFSK-1	brain:	n/a
47	chr8:92220385-92220435	GM06990	blood:	n/a
48	chr8:92221717-92221767	HCT-116	colon:	n/a
49	chr8:92221717-92221767	HAEpiC	amniotic membrane:	n/a
50	chr8:92221717-92221767	T-47D	breast:	n/a

No.	Distal block	Cell Line	Cell type
1	chr8:92213332..92216018-chr8:92217833..92220309,2	K562	blood:
2	chr8:92238980..92241118-chr8:92242981..92244553,2	K562	blood:
3	chr8:92224811..92226448-chr8:92228585..92231288,2	MCF-7	breast:
4	chr8:92213606..92216793-chr8:92216935..92222522,6	K562	blood:
5	chr8:92208641..92211587-chr8:92213183..92215216,2	K562	blood:
6	chr8:92235819..92238487-chr8:92241544..92243410,2	MCF-7	breast:
7	chr8:92213332..92216018-chr8:92217833..92220309,2	K562	blood:
8	chr8:92224876..92227971-chr8:92228140..92231378,3	K562	blood:
9	chr8:92211485..92213094-chr8:92215301..92218291,2	K562	blood:
10	chr8:92185616..92187449-chr8:92210169..92211682,2	K562	blood:
11	chr8:92224811..92226448-chr8:92228585..92231288,2	MCF-7	breast:
12	chr8:92155872..92157525-chr8:92209191..92211411,2	K562	blood:
13	chr8:92218781..92222245-chr8:92222293..92225808,3	K562	blood:
14	chr8:92221069..92223127-chr8:92229716..92232040,2	MCF-7	breast:
15	chr8:92224876..92227971-chr8:92228140..92231378,3	K562	blood:
16	chr8:92208641..92211587-chr8:92213183..92215216,2	K562	blood:

miRNA name	Chromosome Location	mirBase accession
hsa-miR-4661-3p	chr8:92217759-92217780	MIMAT0019730
hsa-miR-4661-5p	chr8:92217722-92217743	MIMAT0019729

Variant related genes	Relation type
SLC26A7	TF binding region
MIR4661	TF binding region
SLC26A7	CpG island
MIR4661	CpG island
ENSG00000147606	chromatin interactions
ENSG00000266194	chromatin interactions

Extended variants
information (count: 1179 )
Associated
traits (count: 110 )

Variant overlapped rSNPs/rCNVs (count:1179 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs568307557	chr8:92204018-92204019	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs535723039	chr8:92204020-92204021	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs529576393	chr8:92204049-92204050	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs550831373	chr8:92204068-92204069	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs13274992	chr8:92204070-92204071	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs562542260	chr8:92204121-92204122	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs62526731	chr8:92204127-92204128	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs140581712	chr8:92204149-92204150	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs13267726	chr8:92204183-92204184	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs13275319	chr8:92204184-92204185	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs577178743	chr8:92204206-92204207	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs28498511	chr8:92204207-92204208	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs539354267	chr8:92204216-92204217	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs188687154	chr8:92204222-92204223	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs199924721	chr8:92204258-92204259	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs575063747	chr8:92204320-92204321	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs542083938	chr8:92204368-92204369	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs563560415	chr8:92204389-92204390	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs372689717	chr8:92204419-92204420	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs200707466	chr8:92204436-92204437	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs575386306	chr8:92204454-92204455	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs545500769	chr8:92204522-92204523	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs564064818	chr8:92204535-92204536	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs558082107	chr8:92204536-92204537	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs528183284	chr8:92204542-92204543	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs546303644	chr8:92204553-92204554	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs375648843	chr8:92204558-92204559	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs371158656	chr8:92204612-92204613	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs561711930	chr8:92204621-92204622	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs529222671	chr8:92204716-92204717	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs201573980	chr8:92204748-92204749	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs550868055	chr8:92204783-92204784	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs569078235	chr8:92204817-92204818	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs539604188	chr8:92204858-92204859	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs551546137	chr8:92204867-92204868	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs570903142	chr8:92204882-92204883	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs200040955	chr8:92204904-92204905	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs200879668	chr8:92204906-92204907	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs181267609	chr8:92204910-92204911	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs186935729	chr8:92204924-92204925	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs190172619	chr8:92204966-92204967	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs7462355	chr8:92204983-92204984	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs575520846	chr8:92205026-92205027	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs4574811	chr8:92205041-92205042	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs370669170	chr8:92205138-92205139	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs572884456	chr8:92205151-92205152	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs540291547	chr8:92205187-92205188	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs187502920	chr8:92205199-92205200	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs59781848	chr8:92205200-92205201	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs191835239	chr8:92205209-92205210	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:110)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Melanoma	18172304	CNVD
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
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Seminomas	18059402	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Testicular cancer	18059402	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Cancer	20164919	CNVD
Esophageal cancer	20955586	CNVD
Multiple myeloma	16461302	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	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	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
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
Glioblastoma multiforme	18628472	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Cancer	21949371	CNVD
Non-small cell lung cancer	21829676	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Acute myeloid leukemia	21358987	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	21399628	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
small cell lung cancer	20016488	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
Bladder cancer	19088036	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
Epilepsy	20502679	CNVD
Breast cancer	20409316	CNVD
Acute myeloid leukemia	19651601	CNVD
head and neck squamous cell carcinoma	19451471	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17170743	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Breast cancer	21611746	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Schizophrenia	23813976	CNVD
Colorectal cancer	21645411	CNVD
Breast cancer	22522925	CNVD
Osteosarcoma	21215367	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:100 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:92202600-92211400	Weak transcription	Right Atrium	heart
2	chr8:92203800-92204000	ZNF genes & repeats	Fetal Intestine Small	intestine
3	chr8:92204000-92205200	Weak transcription	Fetal Intestine Small	intestine
4	chr8:92209600-92209800	Active TSS	H1 Cell Line	embryonic stem cell
5	chr8:92209600-92209800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr8:92209600-92210200	Active TSS	H9 Cell Line	embryonic stem cell
7	chr8:92209600-92210200	Active TSS	HUES48 Cell Line	embryonic stem cell
8	chr8:92209600-92210200	Active TSS	iPS-15b Cell Line	embryonic stem cell
9	chr8:92209600-92210200	Active TSS	iPS-18 Cell Line	embryonic stem cell
10	chr8:92209600-92210200	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
11	chr8:92209600-92210200	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr8:92209600-92210400	Active TSS	ES-WA7 Cell Line	embryonic stem cell
13	chr8:92209600-92210400	Active TSS	Fetal Intestine Large	intestine
14	chr8:92209600-92210400	Active TSS	K562	blood
15	chr8:92209600-92210600	Active TSS	HUES6 Cell Line	embryonic stem cell
16	chr8:92209600-92210600	Active TSS	HUES64 Cell Line	embryonic stem cell
17	chr8:92209600-92210600	Active TSS	iPS-20b Cell Line	embryonic stem cell
18	chr8:92209600-92210600	Active TSS	Fetal Intestine Small	intestine
19	chr8:92209600-92210800	Active TSS	ES-I3 Cell Line	embryonic stem cell
20	chr8:92209800-92210000	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
21	chr8:92209800-92210200	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr8:92209800-92210200	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
23	chr8:92209800-92210200	Active TSS	Rectal Mucosa Donor 31	rectum
24	chr8:92209800-92210400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr8:92210000-92210400	Active TSS	H1 Cell Line	embryonic stem cell
26	chr8:92210200-92210400	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
27	chr8:92210200-92210400	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
28	chr8:92210200-92210400	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
29	chr8:92210400-92210600	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
30	chr8:92210400-92210600	Flanking Active TSS	K562	blood
31	chr8:92210600-92210800	Enhancers	K562	blood
32	chr8:92211200-92211400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr8:92211400-92211600	Enhancers	HUES6 Cell Line	embryonic stem cell
34	chr8:92211400-92211600	Enhancers	HUES64 Cell Line	embryonic stem cell
35	chr8:92216000-92216400	Enhancers	Placenta	Placenta
36	chr8:92216400-92219400	Weak transcription	Placenta	Placenta
37	chr8:92216600-92216800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr8:92216800-92217800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr8:92217200-92218000	Enhancers	Fetal Intestine Large	intestine
40	chr8:92217800-92218200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr8:92218000-92220200	Weak transcription	Fetal Intestine Large	intestine
42	chr8:92219200-92221000	Enhancers	HepG2	liver
43	chr8:92219400-92220200	Enhancers	Placenta	Placenta
44	chr8:92220200-92220800	Enhancers	Fetal Intestine Large	intestine
45	chr8:92220200-92221000	Weak transcription	Placenta	Placenta
46	chr8:92221000-92221200	Enhancers	Placenta	Placenta
47	chr8:92224000-92224400	Enhancers	Pancreatic Islets	Pancreatic Islet
48	chr8:92224000-92226400	Enhancers	Fetal Heart	heart
49	chr8:92225400-92225800	Enhancers	Breast Myoepithelial Primary Cells	Breast
50	chr8:92225400-92226200	Enhancers	Fetal Adrenal Gland	Adrenal Gland

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