Variant report

Variant	nsv972110
Chromosome Location	chr8:86499893-86550441
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	BHLHE40	chr8:86530061-86530136	K562	blood:	n/a	n/a
2	CEBPB	chr8:86505964-86506372	MCF-7	breast:	n/a	chr8:86506202-86506211 chr8:86506200-86506211
3	CEBPB	chr8:86548074-86548266	HepG2	liver:	n/a	chr8:86548177-86548194
4	CEBPB	chr8:86526484-86526818	ECC-1	luminal epithelium:	n/a	chr8:86526677-86526688
5	CEBPB	chr8:86526501-86526858	HepG2	liver:	n/a	chr8:86526677-86526688
6	CEBPB	chr8:86526425-86526941	MCF-7	breast:	n/a	chr8:86526677-86526688
7	CEBPB	chr8:86506011-86506339	MCF-7	breast:	n/a	chr8:86506202-86506211 chr8:86506200-86506211
8	CEBPB	chr8:86526617-86526827	K562	blood:	n/a	chr8:86526677-86526688
9	CEBPB	chr8:86541828-86542028	HepG2	liver:	n/a	chr8:86541944-86541955
10	CEBPB	chr8:86506081-86506340	K562	blood:	n/a	chr8:86506202-86506211 chr8:86506200-86506211
11	CEBPB	chr8:86526496-86526857	IMR90	lung:	n/a	chr8:86526677-86526688
12	CEBPB	chr8:86506026-86506381	A549	lung:	n/a	chr8:86506202-86506211 chr8:86506200-86506211
13	CEBPB	chr8:86506060-86506371	IMR90	lung:	n/a	chr8:86506202-86506211 chr8:86506200-86506211
14	CEBPB	chr8:86526519-86526866	A549	lung:	n/a	chr8:86526677-86526688
15	CEBPB	chr8:86526551-86526947	ECC-1	luminal epithelium:	n/a	chr8:86526677-86526688
16	CEBPB	chr8:86506027-86506610	HepG2	liver:	n/a	chr8:86506202-86506211 chr8:86506581-86506598 chr8:86506488-86506500 chr8:86506200-86506211
17	CEBPB	chr8:86506021-86506349	H1-hESC	embryonic stem cell:	n/a	chr8:86506202-86506211 chr8:86506200-86506211
18	CHD2	chr8:86509594-86509815	H1-hESC	embryonic stem cell:	n/a	n/a
19	CTCF	chr8:86501940-86502090	HRE	kidney:	n/a	n/a
20	CTCF	chr8:86544750-86544836	Pancreas_OC	pancreas:	n/a	n/a
21	CTCF	chr8:86500740-86500890	HCT-116	colon:	n/a	n/a
22	CTCF	chr8:86509421-86509521	Kidney_OC	kidney:	n/a	n/a
23	CTCF	chr8:86520432-86520511	Kidney_OC	kidney:	n/a	n/a
24	CTCF	chr8:86515129-86515167	GM20000	blood:	n/a	n/a
25	CTCF	chr8:86541400-86541550	HA-sp	spinal cord:	n/a	n/a
26	E2F4	chr8:86528535-86528749	MCF10A-Er-Src	breast:	n/a	n/a
27	E2F4	chr8:86547943-86548263	MCF10A-Er-Src	breast:	n/a	n/a
28	E2F4	chr8:86505700-86505895	MCF10A-Er-Src	breast:	n/a	n/a
29	E2F4	chr8:86502777-86502819	MCF10A-Er-Src	breast:	n/a	n/a
30	EBF1	chr8:86548212-86548420	GM12878	blood:	n/a	chr8:86548316-86548326
31	EP300	chr8:86530109-86530133	K562	blood:	n/a	n/a
32	FOS	chr8:86544590-86544994	MCF10A-Er-Src	breast:	n/a	n/a
33	FOS	chr8:86544555-86544966	MCF10A-Er-Src	breast:	n/a	n/a
34	FOS	chr8:86544593-86544999	MCF10A-Er-Src	breast:	n/a	n/a
35	FOS	chr8:86526559-86526927	MCF10A-Er-Src	breast:	n/a	n/a
36	FOS	chr8:86547861-86548371	MCF10A-Er-Src	breast:	n/a	chr8:86548023-86548035
37	FOS	chr8:86526689-86526696	MCF10A-Er-Src	breast:	n/a	n/a
38	FOS	chr8:86547867-86548278	MCF10A-Er-Src	breast:	n/a	chr8:86548023-86548035
39	FOS	chr8:86547885-86548430	MCF10A-Er-Src	breast:	n/a	chr8:86548023-86548035
40	FOS	chr8:86526691-86526802	MCF10A-Er-Src	breast:	n/a	n/a
41	FOS	chr8:86547443-86547509	MCF10A-Er-Src	breast:	n/a	n/a
42	FOS	chr8:86544592-86544996	MCF10A-Er-Src	breast:	n/a	n/a
43	FOS	chr8:86505726-86505871	MCF10A-Er-Src	breast:	n/a	chr8:86505807-86505815
44	FOS	chr8:86547900-86548453	MCF10A-Er-Src	breast:	n/a	chr8:86548023-86548035
45	FOS	chr8:86505653-86505944	MCF10A-Er-Src	breast:	n/a	chr8:86505807-86505815
46	FOSL1	chr8:86544543-86545175	HCT-116	colon:	n/a	n/a
47	FOSL1	chr8:86544544-86545033	HCT-116	colon:	n/a	n/a
48	FOSL2	chr8:86544559-86545076	MCF-7	breast:	n/a	n/a
49	FOXA2	chr8:86507937-86508266	A549	lung:	n/a	n/a
50	GATA2	chr8:86529877-86530241	K562	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:86504072-86504122	HMEC	breast:	n/a
2	chr8:86504072-86504122	HRPEpiC	eye:	n/a
3	chr8:86504072-86504122	BE2_C	brain:	n/a
4	chr8:86504072-86504122	NB4	blood:	n/a
5	chr8:86504072-86504122	HIPEpiC	eye:	n/a
6	chr8:86504072-86504122	H1-hESC	embryonic stem cell:	embryo
7	chr8:86504072-86504122	HUVEC	blood vessel:	n/a
8	chr8:86504072-86504122	HEEpiC	esophagus:	n/a
9	chr8:86504072-86504122	GM12878	blood:	n/a
10	chr8:86504072-86504122	SK-N-SH_RA	brain:	n/a
11	chr8:86504072-86504122	NT2-D1	testis:	n/a
12	chr8:86504072-86504122	HCF	heart:	n/a
13	chr8:86504072-86504122	A549	lung:	n/a
14	chr8:86504072-86504122	HRCEpiC	kidney:	n/a
15	chr8:86504072-86504122	NHDF-neo	bronchial:	n/a
16	chr8:86504072-86504122	AG04450	lung:	fetal
17	chr8:86504072-86504122	HCT-116	colon:	n/a
18	chr8:86504072-86504122	Jurkat	blood:	n/a
19	chr8:86504072-86504122	HL-60	blood:	n/a
20	chr8:86504072-86504122	SAEC	small airway:	n/a
21	chr8:86504072-86504122	RPTEC	kidney:	n/a
22	chr8:86504072-86504122	HepG2	liver:	n/a
23	chr8:86504072-86504122	ovcar-3	ovarian:	n/a
24	chr8:86504072-86504122	HAEpiC	amniotic membrane:	n/a
25	chr8:86504072-86504122	AG10803	skin:	n/a
26	chr8:86504072-86504122	GM19239	blood:	n/a
27	chr8:86504072-86504122	SK-N-MC	brain:	n/a
28	chr8:86504072-86504122	MCF10A-Er-Src	breast:	n/a
29	chr8:86504072-86504122	HEK293	kidney:	embryo
30	chr8:86504072-86504122	HPAEpiC	pulmonary alveolar:	n/a
31	chr8:86504072-86504122	Hela-S3	cervix:	n/a
32	chr8:86504072-86504122	K562	blood:	n/a
33	chr8:86504072-86504122	PANC-1	pancreas:	n/a
34	chr8:86504072-86504122	HCM	heart:	n/a
35	chr8:86504072-86504122	GM12892	blood:	n/a
36	chr8:86504072-86504122	PrEC	prostate:	n/a
37	chr8:86504072-86504122	HCPEpiC	choroid plexus:	n/a
38	chr8:86504072-86504122	Caco-2	colon:	n/a
39	chr8:86504072-86504122	IMR90	lung:	fetal
40	chr8:86504072-86504122	AoSMC	blood vessel:	n/a
41	chr8:86504072-86504122	MCF-7	breast:	n/a
42	chr8:86504072-86504122	CMK	blood:	n/a
43	chr8:86504072-86504122	BJ	skin:	n/a
44	chr8:86504072-86504122	Hepatocyte	liver:	n/a
45	chr8:86504072-86504122	ProgFib	skin:	n/a
46	chr8:86504072-86504122	AG04449	skin:	fetal
47	chr8:86504072-86504122	ECC-1	luminal epithelium:	n/a
48	chr8:86504072-86504122	T-47D	breast:	n/a
49	chr8:86504072-86504122	AG09319	gingival:	n/a
50	chr8:86504072-86504122	GM12891	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr8:86494376..86498242-chr8:86499635..86502661,3	MCF-7	breast:
2	chr8:86439507..86442336-chr8:86514176..86515935,2	MCF-7	breast:
3	chr22:21257752..21260264-chr8:86546631..86548915,2	MCF-7	breast:
4	chr8:86374283..86376503-chr8:86538225..86540669,2	MCF-7	breast:
5	chr8:86375424..86377352-chr8:86545353..86547430,2	MCF-7	breast:
6	chr8:86525634..86527923-chr8:86533854..86535632,2	MCF-7	breast:
7	chr8:86525634..86527923-chr8:86533854..86535632,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-REXO1L1-3	chr8:86509528-86509569	NONHSAT127537
2	lnc-REXO1L1-3	chr8:86508349-86508606	NONHSAT127537

Variant related genes	Relation type
ENSG00000253680	TF binding region
ENSG00000253680	CpG island
ENSG00000104267	chromatin interactions
ENSG00000253549	chromatin interactions

Extended variants
information (count: 1122 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:1122 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs548017109	chr8:86499904-86499905	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs570847911	chr8:86499988-86499989	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs369057103	chr8:86499989-86499990	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs146579215	chr8:86500008-86500009	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs202200372	chr8:86500022-86500023	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs570723435	chr8:86500029-86500030	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs76532698	chr8:86500031-86500032	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs534239556	chr8:86500045-86500046	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs201625637	chr8:86500056-86500057	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs143660294	chr8:86500067-86500068	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs115082213	chr8:86500080-86500081	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs535715901	chr8:86500082-86500083	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs555711797	chr8:86500099-86500100	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs572227005	chr8:86500195-86500196	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs534511695	chr8:86500198-86500199	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs557970929	chr8:86500238-86500239	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs141179600	chr8:86500261-86500262	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs543534676	chr8:86500295-86500296	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs562917299	chr8:86500344-86500345	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs573319227	chr8:86500345-86500346	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs376116014	chr8:86500367-86500368	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs75785193	chr8:86500381-86500382	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs186095354	chr8:86500419-86500420	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs375337500	chr8:86500420-86500421	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs528028920	chr8:86500427-86500428	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs547659646	chr8:86500449-86500450	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs148306104	chr8:86500481-86500482	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs112046986	chr8:86500505-86500506	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs550311719	chr8:86500515-86500516	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs574454479	chr8:86500518-86500519	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs370844929	chr8:86500520-86500521	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs150386593	chr8:86500521-86500522	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs373729308	chr8:86500615-86500616	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs377681826	chr8:86500643-86500644	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs138110620	chr8:86500649-86500650	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs71525007	chr8:86500656-86500657	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs565973622	chr8:86500674-86500675	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs370859942	chr8:86500725-86500726	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs143632683	chr8:86500736-86500737	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs59707884	chr8:86500762-86500763	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs577791718	chr8:86500798-86500799	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs190510077	chr8:86500800-86500801	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs368970003	chr8:86500804-86500805	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs536713693	chr8:86500805-86500806	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs546879130	chr8:86500846-86500847	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs573255437	chr8:86500847-86500848	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs542206276	chr8:86500863-86500864	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs558956995	chr8:86500884-86500885	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs181437348	chr8:86500946-86500947	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs541730979	chr8:86500989-86500990	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:104)

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
Acute lymphoblastic leukemia	22237106	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
Acute monocytic leukemia	16498392	CNVD
Autism	20841430	CNVD
Colorectal cancer	21645411	CNVD
Breast cancer	21364760	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:215 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:86495000-86500200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
2	chr8:86500200-86500800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
3	chr8:86500800-86504400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
4	chr8:86502000-86502200	Enhancers	Thymus	Thymus
5	chr8:86502000-86502400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr8:86502000-86503000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr8:86502200-86502400	Enhancers	H1 Cell Line	embryonic stem cell
8	chr8:86502200-86502400	Enhancers	Brain Angular Gyrus	brain
9	chr8:86502200-86502400	Enhancers	Stomach Mucosa	stomach
10	chr8:86502200-86503600	Enhancers	HUES48 Cell Line	embryonic stem cell
11	chr8:86502200-86503800	Enhancers	HUES6 Cell Line	embryonic stem cell
12	chr8:86502200-86504000	Enhancers	iPS-20b Cell Line	embryonic stem cell
13	chr8:86502200-86508600	Weak transcription	Thymus	Thymus
14	chr8:86502400-86504000	Weak transcription	H1 Cell Line	embryonic stem cell
15	chr8:86502400-86504000	Weak transcription	Brain Angular Gyrus	brain
16	chr8:86502400-86506200	Enhancers	iPS-18 Cell Line	embryonic stem cell
17	chr8:86502400-86508400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
18	chr8:86502600-86502800	Weak transcription	Brain Cingulate Gyrus	brain
19	chr8:86502600-86504000	Weak transcription	Stomach Mucosa	stomach
20	chr8:86502600-86505800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
21	chr8:86502600-86506400	Enhancers	HUES64 Cell Line	embryonic stem cell
22	chr8:86502800-86503000	Enhancers	Brain Cingulate Gyrus	brain
23	chr8:86502800-86503400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr8:86503000-86505200	Weak transcription	Brain Cingulate Gyrus	brain
25	chr8:86503000-86508200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr8:86503200-86503800	Enhancers	iPS-15b Cell Line	embryonic stem cell
27	chr8:86503200-86503800	Enhancers	Brain Hippocampus Middle	brain
28	chr8:86503200-86504600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr8:86503200-86504600	Enhancers	Brain Substantia Nigra	brain
30	chr8:86503200-86506800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
31	chr8:86503400-86503800	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr8:86503400-86504200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr8:86503600-86503800	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
34	chr8:86503600-86504200	Active TSS	ES-WA7 Cell Line	embryonic stem cell
35	chr8:86503600-86504200	Enhancers	Primary T cells from cord blood	blood
36	chr8:86503600-86504200	Active TSS	Brain Anterior Caudate	brain
37	chr8:86503800-86504000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr8:86503800-86504000	Enhancers	HUES48 Cell Line	embryonic stem cell
39	chr8:86503800-86504200	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
40	chr8:86503800-86504200	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
41	chr8:86503800-86505200	Weak transcription	Brain Hippocampus Middle	brain
42	chr8:86504000-86504200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
43	chr8:86504000-86504200	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr8:86504000-86504200	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
45	chr8:86504000-86504200	Enhancers	Brain Angular Gyrus	brain
46	chr8:86504000-86504200	Enhancers	Fetal Kidney	kidney
47	chr8:86504000-86504200	Enhancers	Stomach Mucosa	stomach
48	chr8:86504000-86504400	Enhancers	H1 Cell Line	embryonic stem cell
49	chr8:86504000-86504400	Enhancers	H9 Cell Line	embryonic stem cell
50	chr8:86504000-86504400	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell

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