Variant report

Variant	nsv891131
Chromosome Location	chr8:86501203-86560123
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:417)
CpG islands
(count:549)
Chromatin interactive
region (count:7)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:417 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr8:86559452-86559628	GM12878	blood:	n/a	n/a
2	BATF	chr8:86557168-86557577	GM12878	blood:	n/a	n/a
3	BATF	chr8:86557171-86557645	GM12878	blood:	n/a	n/a
4	BATF	chr8:86556713-86557155	GM12878	blood:	n/a	n/a
5	BATF	chr8:86556634-86557157	GM12878	blood:	n/a	n/a
6	BATF	chr8:86559441-86559628	GM12878	blood:	n/a	n/a
7	BATF	chr8:86559222-86559386	GM12878	blood:	n/a	n/a
8	BCL11A	chr8:86559434-86559714	GM12878	blood:	n/a	n/a
9	BCL11A	chr8:86559452-86559688	GM12878	blood:	n/a	n/a
10	BCL11A	chr8:86557628-86557805	GM12878	blood:	n/a	n/a
11	BCL11A	chr8:86557171-86557821	GM12878	blood:	n/a	chr8:86557185-86557194
12	BCL11A	chr8:86559954-86560254	GM12878	blood:	n/a	n/a
13	BCL11A	chr8:86559910-86560168	GM12878	blood:	n/a	n/a
14	BCL11A	chr8:86556627-86557168	GM12878	blood:	n/a	n/a
15	BCL11A	chr8:86556646-86557544	GM12878	blood:	n/a	chr8:86557185-86557194 chr8:86557162-86557171
16	BCL11A	chr8:86556317-86556493	GM12878	blood:	n/a	n/a
17	BHLHE40	chr8:86530061-86530136	K562	blood:	n/a	n/a
18	BHLHE40	chr8:86556653-86557165	HepG2	liver:	n/a	n/a
19	BHLHE40	chr8:86557188-86557731	HepG2	liver:	n/a	n/a
20	CEBPB	chr8:86526501-86526858	HepG2	liver:	n/a	chr8:86526677-86526688
21	CEBPB	chr8:86548074-86548266	HepG2	liver:	n/a	chr8:86548177-86548194
22	CEBPB	chr8:86506021-86506349	H1-hESC	embryonic stem cell:	n/a	chr8:86506202-86506211 chr8:86506200-86506211
23	CEBPB	chr8:86506026-86506381	A549	lung:	n/a	chr8:86506202-86506211 chr8:86506200-86506211
24	CEBPB	chr8:86526617-86526827	K562	blood:	n/a	chr8:86526677-86526688
25	CEBPB	chr8:86526551-86526947	ECC-1	luminal epithelium:	n/a	chr8:86526677-86526688
26	CEBPB	chr8:86505964-86506372	MCF-7	breast:	n/a	chr8:86506202-86506211 chr8:86506200-86506211
27	CEBPB	chr8:86506060-86506371	IMR90	lung:	n/a	chr8:86506202-86506211 chr8:86506200-86506211
28	CEBPB	chr8:86526519-86526866	A549	lung:	n/a	chr8:86526677-86526688
29	CEBPB	chr8:86541828-86542028	HepG2	liver:	n/a	chr8:86541944-86541955
30	CEBPB	chr8:86506027-86506610	HepG2	liver:	n/a	chr8:86506202-86506211 chr8:86506581-86506598 chr8:86506488-86506500 chr8:86506200-86506211
31	CEBPB	chr8:86506081-86506340	K562	blood:	n/a	chr8:86506202-86506211 chr8:86506200-86506211
32	CEBPB	chr8:86526496-86526857	IMR90	lung:	n/a	chr8:86526677-86526688
33	CEBPB	chr8:86526425-86526941	MCF-7	breast:	n/a	chr8:86526677-86526688
34	CEBPB	chr8:86526484-86526818	ECC-1	luminal epithelium:	n/a	chr8:86526677-86526688
35	CEBPB	chr8:86506011-86506339	MCF-7	breast:	n/a	chr8:86506202-86506211 chr8:86506200-86506211
36	CHD2	chr8:86509594-86509815	H1-hESC	embryonic stem cell:	n/a	n/a
37	CTCF	chr8:86515129-86515167	GM20000	blood:	n/a	n/a
38	CTCF	chr8:86544750-86544836	Pancreas_OC	pancreas:	n/a	n/a
39	CTCF	chr8:86557745-86557781	MCF-7	breast:	n/a	n/a
40	CTCF	chr8:86509421-86509521	Kidney_OC	kidney:	n/a	n/a
41	CTCF	chr8:86557746-86557784	A549	lung:	n/a	n/a
42	CTCF	chr8:86557750-86557805	HepG2	liver:	n/a	n/a
43	CTCF	chr8:86541400-86541550	HA-sp	spinal cord:	n/a	n/a
44	CTCF	chr8:86501940-86502090	HRE	kidney:	n/a	n/a
45	CTCF	chr8:86557770-86557778	Gliobla	brain:	n/a	n/a
46	CTCF	chr8:86520432-86520511	Kidney_OC	kidney:	n/a	n/a
47	CTCF	chr8:86557743-86557830	MCF-7	breast:	n/a	n/a
48	E2F4	chr8:86528535-86528749	MCF10A-Er-Src	breast:	n/a	n/a
49	E2F4	chr8:86547943-86548263	MCF10A-Er-Src	breast:	n/a	n/a
50	E2F4	chr8:86505700-86505895	MCF10A-Er-Src	breast:	n/a	n/a

(count:549 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:86554026-86554076	A549	lung:	n/a
2	chr8:86504072-86504122	HCPEpiC	choroid plexus:	n/a
3	chr8:86554026-86554076	HRCEpiC	kidney:	n/a
4	chr8:86551492-86551542	NB4	blood:	n/a
5	chr8:86551492-86551542	ovcar-3	ovarian:	n/a
6	chr8:86556749-86556799	A549	lung:	n/a
7	chr8:86556903-86556953	A549	lung:	n/a
8	chr8:86556749-86556799	HL-60	blood:	n/a
9	chr8:86556171-86556221	ovcar-3	ovarian:	n/a
10	chr8:86556171-86556221	HRE	kidney:	n/a
11	chr8:86556164-86556214	NT2-D1	testis:	n/a
12	chr8:86551492-86551542	GM12892	blood:	n/a
13	chr8:86556176-86556226	SK-N-SH_RA	brain:	n/a
14	chr8:86556176-86556226	ovcar-3	ovarian:	n/a
15	chr8:86556749-86556799	HRE	kidney:	n/a
16	chr8:86554888-86554938	HepG2	liver:	n/a
17	chr8:86551492-86551542	AG09309	skin:	n/a
18	chr8:86556171-86556221	T-47D	breast:	n/a
19	chr8:86556903-86556953	Jurkat	blood:	n/a
20	chr8:86556164-86556214	HL-60	blood:	n/a
21	chr8:86551492-86551542	BJ	skin:	n/a
22	chr8:86556176-86556226	LNCaP	prostate:	n/a
23	chr8:86556176-86556226	AG04449	skin:	fetal
24	chr8:86504072-86504122	HIPEpiC	eye:	n/a
25	chr8:86556176-86556226	NT2-D1	testis:	n/a
26	chr8:86556171-86556221	Caco-2	colon:	n/a
27	chr8:86554888-86554938	BE2_C	brain:	n/a
28	chr8:86554888-86554938	MCF-7	breast:	n/a
29	chr8:86551492-86551542	IMR90	lung:	fetal
30	chr8:86551492-86551542	SK-N-MC	brain:	n/a
31	chr8:86504072-86504122	BJ	skin:	n/a
32	chr8:86504072-86504122	PANC-1	pancreas:	n/a
33	chr8:86504072-86504122	PFSK-1	brain:	n/a
34	chr8:86551492-86551542	HRE	kidney:	n/a
35	chr8:86556903-86556953	SK-N-SH	brain:	n/a
36	chr8:86556749-86556799	H1-hESC	embryonic stem cell:	embryo
37	chr8:86554026-86554076	HCPEpiC	choroid plexus:	n/a
38	chr8:86551492-86551542	MCF-7	breast:	n/a
39	chr8:86556164-86556214	PrEC	prostate:	n/a
40	chr8:86554026-86554076	HAEpiC	amniotic membrane:	n/a
41	chr8:86556903-86556953	NHDF-neo	bronchial:	n/a
42	chr8:86504072-86504122	BE2_C	brain:	n/a
43	chr8:86556903-86556953	HepG2	liver:	n/a
44	chr8:86551492-86551542	LNCaP	prostate:	n/a
45	chr8:86551492-86551542	MCF10A-Er-Src	breast:	n/a
46	chr8:86556903-86556953	AG09309	skin:	n/a
47	chr8:86556171-86556221	SAEC	small airway:	n/a
48	chr8:86556176-86556226	AoSMC	blood vessel:	n/a
49	chr8:86504072-86504122	SKMC	muscle:	n/a
50	chr8:86556164-86556214	HCM	heart:	n/a

(count:7 , 50 per page) page: 1

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

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

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

No data

Variant related genes	Relation type
ENSG00000253680	TF binding region
REXO1L8P	TF binding region
ENSG00000253680	CpG island
REXO1L8P	CpG island
ENSG00000253549	chromatin interactions
ENSG00000104267	chromatin interactions

Extended variants
information (count: 1345 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:1345 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7823943	chr8:86501203-86501204	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs529453000	chr8:86501249-86501250	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs111796066	chr8:86501300-86501301	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs201645457	chr8:86501307-86501308	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs78161237	chr8:86501311-86501312	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs534588125	chr8:86501328-86501329	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs551671801	chr8:86501378-86501379	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs571316098	chr8:86501379-86501380	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs536852402	chr8:86501382-86501383	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs556784598	chr8:86501447-86501448	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs183266400	chr8:86501450-86501451	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs187743377	chr8:86501532-86501533	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs552521897	chr8:86501539-86501540	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs563513506	chr8:86501584-86501585	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs377009588	chr8:86501650-86501651	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs572810508	chr8:86501680-86501681	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs541319825	chr8:86501715-86501716	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs566734437	chr8:86501718-86501719	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs558428085	chr8:86501721-86501722	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs140418344	chr8:86501727-86501728	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs189699298	chr8:86501733-86501734	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs67823411	chr8:86501743-86501744	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs563284373	chr8:86501744-86501745	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs530964826	chr8:86501772-86501773	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs544018321	chr8:86501835-86501836	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs207469492	chr8:86501841-86501842	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs149237739	chr8:86501870-86501871	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs368748558	chr8:86501887-86501888	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs529387265	chr8:86501973-86501974	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs540399173	chr8:86502046-86502047	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs559455918	chr8:86502050-86502051	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs559624935	chr8:86502058-86502059	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs144431780	chr8:86502077-86502078	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs571515355	chr8:86502215-86502216	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs183390376	chr8:86502219-86502220	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs187791183	chr8:86502230-86502231	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs567145122	chr8:86502274-86502275	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs535908908	chr8:86502297-86502298	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs553040751	chr8:86502319-86502320	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs566296099	chr8:86502413-86502414	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs115776056	chr8:86502502-86502503	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs558306337	chr8:86502550-86502551	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs192228545	chr8:86502554-86502555	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs185298101	chr8:86502585-86502586	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs367639892	chr8:86502660-86502661	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs371770324	chr8:86502671-86502672	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs188564821	chr8:86502684-86502685	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs543104979	chr8:86502694-86502695	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs548367639	chr8:86502710-86502711	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs559801027	chr8:86502758-86502759	Weak transcription Enhancers	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:214 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:86500800-86504400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
2	chr8:86502000-86502200	Enhancers	Thymus	Thymus
3	chr8:86502000-86502400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr8:86502000-86503000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr8:86502200-86502400	Enhancers	H1 Cell Line	embryonic stem cell
6	chr8:86502200-86502400	Enhancers	Brain Angular Gyrus	brain
7	chr8:86502200-86502400	Enhancers	Stomach Mucosa	stomach
8	chr8:86502200-86503600	Enhancers	HUES48 Cell Line	embryonic stem cell
9	chr8:86502200-86503800	Enhancers	HUES6 Cell Line	embryonic stem cell
10	chr8:86502200-86504000	Enhancers	iPS-20b Cell Line	embryonic stem cell
11	chr8:86502200-86508600	Weak transcription	Thymus	Thymus
12	chr8:86502400-86504000	Weak transcription	H1 Cell Line	embryonic stem cell
13	chr8:86502400-86504000	Weak transcription	Brain Angular Gyrus	brain
14	chr8:86502400-86506200	Enhancers	iPS-18 Cell Line	embryonic stem cell
15	chr8:86502400-86508400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
16	chr8:86502600-86502800	Weak transcription	Brain Cingulate Gyrus	brain
17	chr8:86502600-86504000	Weak transcription	Stomach Mucosa	stomach
18	chr8:86502600-86505800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
19	chr8:86502600-86506400	Enhancers	HUES64 Cell Line	embryonic stem cell
20	chr8:86502800-86503000	Enhancers	Brain Cingulate Gyrus	brain
21	chr8:86502800-86503400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr8:86503000-86505200	Weak transcription	Brain Cingulate Gyrus	brain
23	chr8:86503000-86508200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr8:86503200-86503800	Enhancers	iPS-15b Cell Line	embryonic stem cell
25	chr8:86503200-86503800	Enhancers	Brain Hippocampus Middle	brain
26	chr8:86503200-86504600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr8:86503200-86504600	Enhancers	Brain Substantia Nigra	brain
28	chr8:86503200-86506800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
29	chr8:86503400-86503800	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr8:86503400-86504200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr8:86503600-86503800	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
32	chr8:86503600-86504200	Active TSS	ES-WA7 Cell Line	embryonic stem cell
33	chr8:86503600-86504200	Enhancers	Primary T cells from cord blood	blood
34	chr8:86503600-86504200	Active TSS	Brain Anterior Caudate	brain
35	chr8:86503800-86504000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr8:86503800-86504000	Enhancers	HUES48 Cell Line	embryonic stem cell
37	chr8:86503800-86504200	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
38	chr8:86503800-86504200	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
39	chr8:86503800-86505200	Weak transcription	Brain Hippocampus Middle	brain
40	chr8:86504000-86504200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
41	chr8:86504000-86504200	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr8:86504000-86504200	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
43	chr8:86504000-86504200	Enhancers	Brain Angular Gyrus	brain
44	chr8:86504000-86504200	Enhancers	Fetal Kidney	kidney
45	chr8:86504000-86504200	Enhancers	Stomach Mucosa	stomach
46	chr8:86504000-86504400	Enhancers	H1 Cell Line	embryonic stem cell
47	chr8:86504000-86504400	Enhancers	H9 Cell Line	embryonic stem cell
48	chr8:86504000-86504400	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
49	chr8:86504000-86506000	Enhancers	ES-I3 Cell Line	embryonic stem cell
50	chr8:86504200-86504600	Enhancers	HUES48 Cell Line	embryonic stem cell

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