Variant report

Variant	nsv611646
Chromosome Location	chr8:85048690-85112377
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:346)
CpG islands
(count:1343)
Chromatin interactive
region (count:1)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:346 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr8:85094372-85094687	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr8:85096875-85097265	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr8:85094981-85095827	H1-hESC	embryonic stem cell:	n/a	n/a
4	CEBPB	chr8:85087477-85087835	HepG2	liver:	n/a	chr8:85087656-85087667
5	CEBPB	chr8:85094566-85094736	H1-hESC	embryonic stem cell:	n/a	n/a
6	CEBPB	chr8:85091837-85092085	HepG2	liver:	n/a	chr8:85091966-85091977
7	CHD1	chr8:85094617-85094762	H1-hESC	embryonic stem cell:	n/a	n/a
8	CHD1	chr8:85095657-85096073	H1-hESC	embryonic stem cell:	n/a	n/a
9	CTBP2	chr8:85094338-85095741	H1-hESC	embryonic stem cell:	n/a	n/a
10	CTBP2	chr8:85096544-85097365	H1-hESC	embryonic stem cell:	n/a	n/a
11	CTCF	chr8:85099278-85099280	LNCaP	prostate:	n/a	n/a
12	CTCF	chr8:85094531-85094573	GM13976	blood:	n/a	n/a
13	CTCF	chr8:85078600-85078750	MCF-7	breast:	n/a	n/a
14	CTCF	chr8:85099040-85099190	K562	blood:	n/a	chr8:85099160-85099173 chr8:85099158-85099176
15	CTCF	chr8:85099060-85099210	HEEpiC	esophagus:	n/a	chr8:85099160-85099173 chr8:85099158-85099176
16	CTCF	chr8:85095520-85095670	SK-N-SH_RA	brain:	n/a	n/a
17	CTCF	chr8:85095960-85096110	HBMEC	blood vessel:	n/a	n/a
18	CTCF	chr8:85094640-85094790	GM12875	blood:	n/a	n/a
19	CTCF	chr8:85099120-85099270	HepG2	liver:	n/a	chr8:85099160-85099173 chr8:85099158-85099176
20	CTCF	chr8:85099130-85099240	GM13977	blood:	n/a	chr8:85099160-85099173 chr8:85099158-85099176
21	CTCF	chr8:85094480-85094630	HEEpiC	esophagus:	n/a	n/a
22	CTCF	chr8:85099060-85099210	HRPEpiC	eye:	n/a	chr8:85099160-85099173 chr8:85099158-85099176
23	CTCF	chr8:85099100-85099250	HEK293	kidney:	n/a	chr8:85099160-85099173 chr8:85099158-85099176
24	CTCF	chr8:85099027-85099240	SK-N-SH_RA	brain:	n/a	chr8:85099160-85099173 chr8:85099158-85099176
25	CTCF	chr8:85096935-85097007	H1-hESC	embryonic stem cell:	n/a	n/a
26	CTCF	chr8:85094540-85094690	GM12871	blood:	n/a	n/a
27	CTCF	chr8:85094469-85094640	HepG2	liver:	n/a	n/a
28	CTCF	chr8:85095445-85095616	MCF-7	breast:	n/a	n/a
29	CTCF	chr8:85094420-85094682	H1-hESC	embryonic stem cell:	n/a	n/a
30	CTCF	chr8:85094464-85094658	GM19239	blood:	n/a	n/a
31	CTCF	chr8:85099140-85099290	GM12869	blood:	n/a	chr8:85099160-85099173 chr8:85099158-85099176
32	CTCF	chr8:85094506-85094652	LNCaP	prostate:	n/a	n/a
33	CTCF	chr8:85099103-85099241	Pancreas_OC	pancreas:	n/a	chr8:85099160-85099173 chr8:85099158-85099176
34	CTCF	chr8:85094540-85094690	GM12864	blood:	n/a	n/a
35	CTCF	chr8:85094538-85094609	LNCaP	prostate:	n/a	n/a
36	CTCF	chr8:85094480-85094630	SK-N-SH_RA	brain:	n/a	n/a
37	CTCF	chr8:85094600-85094750	HAc	cerebellar:	n/a	n/a
38	CTCF	chr8:85096100-85096250	HEEpiC	esophagus:	n/a	n/a
39	CTCF	chr8:85094460-85094669	A549	lung:	n/a	n/a
40	CTCF	chr8:85098989-85099207	HepG2	liver:	n/a	chr8:85099160-85099173 chr8:85099158-85099176
41	CTCF	chr8:85096040-85096190	BE2_C	brain:	n/a	n/a
42	CTCF	chr8:85095559-85095565	GM12891	blood:	n/a	n/a
43	CTCF	chr8:85094440-85094673	MCF-7	breast:	n/a	n/a
44	CTCF	chr8:85094471-85094640	Pancreas_OC	pancreas:	n/a	n/a
45	CTCF	chr8:85096040-85096190	HEEpiC	esophagus:	n/a	n/a
46	CTCF	chr8:85094440-85094590	HAc	cerebellar:	n/a	n/a
47	CTCF	chr8:85095940-85096090	HEK293	kidney:	n/a	n/a
48	CTCF	chr8:85094500-85094650	HA-sp	spinal cord:	n/a	n/a
49	CTCF	chr8:85094520-85094670	GM12871	blood:	n/a	n/a
50	CTCF	chr8:85098820-85098970	HEEpiC	esophagus:	n/a	n/a

(count:1343 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:85097246-85097296	HRCEpiC	kidney:	n/a
2	chr8:85097246-85097296	HRCEpiC	kidney:	n/a
3	chr8:85095394-85095444	Hepatocyte	liver:	n/a
4	chr8:85097056-85097106	U87	brain:	n/a
5	chr8:85097031-85097081	ovcar-3	ovarian:	n/a
6	chr8:85097157-85097207	PANC-1	pancreas:	n/a
7	chr8:85094842-85094892	BJ	skin:	n/a
8	chr8:85095654-85095704	Hepatocyte	liver:	n/a
9	chr8:85097429-85097479	HEK293	kidney:	embryo
10	chr8:85096868-85096918	PANC-1	pancreas:	n/a
11	chr8:85097246-85097296	SKMC	muscle:	n/a
12	chr8:85097056-85097106	GM12892	blood:	n/a
13	chr8:85095654-85095704	BE2_C	brain:	n/a
14	chr8:85097157-85097207	ProgFib	skin:	n/a
15	chr8:85095697-85095747	HIPEpiC	eye:	n/a
16	chr8:85097195-85097245	MCF10A-Er-Src	breast:	n/a
17	chr8:85095654-85095704	U87	brain:	n/a
18	chr8:85094923-85094973	ECC-1	luminal epithelium:	n/a
19	chr8:85095394-85095444	GM19239	blood:	n/a
20	chr8:85094904-85094954	HRE	kidney:	n/a
21	chr8:85097056-85097106	GM06990	blood:	n/a
22	chr8:85097056-85097106	HCM	heart:	n/a
23	chr8:85096037-85096087	HMEC	breast:	n/a
24	chr8:85094904-85094954	HEEpiC	esophagus:	n/a
25	chr8:85094437-85094487	GM12878	blood:	n/a
26	chr8:85095394-85095444	Jurkat	blood:	n/a
27	chr8:85094923-85094973	NT2-D1	testis:	n/a
28	chr8:85096037-85096087	AG09309	skin:	n/a
29	chr8:85094742-85094792	PrEC	prostate:	n/a
30	chr8:85097049-85097099	HEK293	kidney:	embryo
31	chr8:85094923-85094973	SK-N-SH_RA	brain:	n/a
32	chr8:85097031-85097081	PrEC	prostate:	n/a
33	chr8:85087913-85087963	HCT-116	colon:	n/a
34	chr8:85095654-85095704	AG09309	skin:	n/a
35	chr8:85095654-85095704	SK-N-SH_RA	brain:	n/a
36	chr8:85096868-85096918	CMK	blood:	n/a
37	chr8:85095275-85095325	NH-A	brain:	n/a
38	chr8:85096037-85096087	HCF	heart:	n/a
39	chr8:85094742-85094792	HCM	heart:	n/a
40	chr8:85094437-85094487	ovcar-3	ovarian:	n/a
41	chr8:85097031-85097081	IMR90	lung:	fetal
42	chr8:85094742-85094792	RPTEC	kidney:	n/a
43	chr8:85095394-85095444	AG09309	skin:	n/a
44	chr8:85095654-85095704	GM19239	blood:	n/a
45	chr8:85096037-85096087	K562	blood:	n/a
46	chr8:85095654-85095704	AoSMC	blood vessel:	n/a
47	chr8:85095697-85095747	A549	lung:	n/a
48	chr8:85097429-85097479	Caco-2	colon:	n/a
49	chr8:85095498-85095548	HAEpiC	amniotic membrane:	n/a
50	chr8:85096868-85096918	HEEpiC	esophagus:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr3:151984232..151987192-chr8:85083866..85086798,2	MCF-7	breast:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RALYL-1	chr8:85052158-85052518	ENSG00000254202
2	lnc-C8orf59-6	chr8:85076737-85076799	NONHSAT127501
3	lnc-C8orf59-6	chr8:85075684-85075888	NONHSAT127501
4	lnc-C8orf59-6	chr8:85076572-85076653	NONHSAT127501
5	lnc-C8orf59-6	chr8:85076228-85076258	NONHSAT127501
6	lnc-RALYL-3	chr8:85074353-85074706	NONHSAT127500

No data

Variant related genes	Relation type
ENSG00000253362	TF binding region
TPM3P3	TF binding region
RALYL	TF binding region
ENSG00000253362	CpG island
TPM3P3	CpG island
RALYL	CpG island
ENSG00000152601	chromatin interactions

Extended variants
information (count: 1190 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:1190 , 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	rs563110384	chr8:85052162-85052163	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
2	rs576026670	chr8:85052193-85052194	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
3	rs28504263	chr8:85052206-85052207	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
4	rs563870670	chr8:85052222-85052223	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
5	rs561306788	chr8:85052273-85052274	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
6	rs184236518	chr8:85052309-85052310	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
7	rs547287003	chr8:85052356-85052357	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
8	rs187761634	chr8:85052382-85052383	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
9	rs533134639	chr8:85052386-85052387	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
10	rs549676246	chr8:85052387-85052388	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
11	rs13274795	chr8:85052428-85052429	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs192339109	chr8:85052430-85052431	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
13	rs548713073	chr8:85052433-85052434	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
14	rs368051122	chr8:85052488-85052489	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
15	rs568458356	chr8:85052517-85052518	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
16	rs566719370	chr8:85055644-85055645	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs556431246	chr8:85055669-85055670	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs538560514	chr8:85055689-85055690	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs558689963	chr8:85055691-85055692	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs532690859	chr8:85055694-85055695	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs73689624	chr8:85055704-85055705	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs577884132	chr8:85055749-85055750	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs16912487	chr8:85055763-85055764	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs368877471	chr8:85055820-85055821	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs201343337	chr8:85055824-85055825	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs557058675	chr8:85055827-85055828	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs573692136	chr8:85055828-85055829	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs398067991	chr8:85055837-85055838	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs67282858	chr8:85055838-85055839	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs200195277	chr8:85055840-85055841	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs542649978	chr8:85055884-85055885	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs16912491	chr8:85055919-85055920	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs528758493	chr8:85055935-85055936	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs545395914	chr8:85055961-85055962	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs721743	chr8:85056014-85056015	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs531159168	chr8:85056033-85056034	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs146744232	chr8:85056064-85056065	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs567410229	chr8:85056118-85056119	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs547806133	chr8:85056119-85056120	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs546572703	chr8:85056155-85056156	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs112208310	chr8:85056180-85056181	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs530109366	chr8:85056185-85056186	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs376021179	chr8:85056238-85056239	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs721742	chr8:85056243-85056244	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs192639176	chr8:85056274-85056275	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs1370417	chr8:85056283-85056284	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
47	rs561114280	chr8:85056325-85056326	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs111369580	chr8:85056386-85056387	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs115967568	chr8:85056457-85056458	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs112685731	chr8:85056556-85056557	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:102)

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
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD

Chromatin state (count:382 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:85055600-85056600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr8:85067400-85067800	Enhancers	Placenta Amnion	Placenta Amnion
3	chr8:85081200-85081800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr8:85085200-85085400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr8:85085200-85086000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr8:85085400-85086600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr8:85085800-85086000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr8:85085800-85086200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
9	chr8:85086000-85087400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr8:85086200-85087200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
11	chr8:85086200-85087400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr8:85086600-85088800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr8:85087200-85087600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr8:85087200-85088400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
15	chr8:85087200-85089000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
16	chr8:85087400-85088800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr8:85087400-85088800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr8:85087400-85088800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
19	chr8:85087600-85088400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
20	chr8:85088400-85088600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
21	chr8:85088600-85089000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
22	chr8:85088800-85094000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
23	chr8:85089000-85089200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
24	chr8:85090400-85092800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
25	chr8:85092800-85093400	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
26	chr8:85092800-85093600	Enhancers	iPS-15b Cell Line	embryonic stem cell
27	chr8:85092800-85094400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
28	chr8:85093000-85093200	Enhancers	iPS-18 Cell Line	embryonic stem cell
29	chr8:85093000-85093200	Enhancers	iPS-20b Cell Line	embryonic stem cell
30	chr8:85093000-85093400	Enhancers	HUES64 Cell Line	embryonic stem cell
31	chr8:85093000-85093800	Enhancers	HUES48 Cell Line	embryonic stem cell
32	chr8:85093000-85093800	Enhancers	HUES6 Cell Line	embryonic stem cell
33	chr8:85093200-85093400	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
34	chr8:85093400-85093800	Enhancers	iPS-18 Cell Line	embryonic stem cell
35	chr8:85093400-85094000	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
36	chr8:85093800-85094000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
37	chr8:85093800-85094000	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
38	chr8:85093800-85094000	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
39	chr8:85093800-85094000	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
40	chr8:85093800-85094200	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell
41	chr8:85093800-85096600	Active TSS	Fetal Brain Female	brain
42	chr8:85093800-85097600	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
43	chr8:85093800-85097600	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
44	chr8:85094000-85094200	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
45	chr8:85094000-85094200	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
46	chr8:85094000-85094200	Active TSS	Brain Germinal Matrix	brain
47	chr8:85094000-85094200	Bivalent Enhancer	Fetal Intestine Small	intestine
48	chr8:85094000-85094400	Bivalent Enhancer	Ganglion Eminence derived primary cultured neurospheres	brain
49	chr8:85094000-85094400	Active TSS	Brain Inferior Temporal Lobe	brain
50	chr8:85094000-85094400	Flanking Active TSS	Fetal Adrenal Gland	Adrenal Gland

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