Variant report

Variant	esv3433426
Chromosome Location	chr8:67859447-67876356
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:226)
CpG islands
(count:916)
Chromatin interactive
region (count:14)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:226 , 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	BACH1	chr8:67874270-67875448	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr8:67873482-67873629	H1-hESC	embryonic stem cell:	n/a	n/a
3	CEBPB	chr8:67874115-67874315	H1-hESC	embryonic stem cell:	n/a	n/a
4	CHD1	chr8:67873613-67873754	H1-hESC	embryonic stem cell:	n/a	n/a
5	CHD1	chr8:67874132-67874239	H1-hESC	embryonic stem cell:	n/a	n/a
6	CHD1	chr8:67875485-67875614	H1-hESC	embryonic stem cell:	n/a	n/a
7	CHD1	chr8:67875035-67875272	H1-hESC	embryonic stem cell:	n/a	n/a
8	CHD2	chr8:67873556-67873737	H1-hESC	embryonic stem cell:	n/a	n/a
9	CHD2	chr8:67874706-67875230	H1-hESC	embryonic stem cell:	n/a	n/a
10	CHD2	chr8:67874135-67874162	H1-hESC	embryonic stem cell:	n/a	n/a
11	CTBP2	chr8:67873439-67874731	H1-hESC	embryonic stem cell:	n/a	n/a
12	CTCF	chr8:67875120-67875270	HPAF	blood vessel:	n/a	n/a
13	CTCF	chr8:67875080-67875230	RPTEC	kidney:	n/a	n/a
14	CTCF	chr8:67860200-67860350	HCPEpiC	choroid plexus:	n/a	chr8:67860271-67860280
15	CTCF	chr8:67874960-67875110	HFF	foreskin:	n/a	n/a
16	CTCF	chr8:67860200-67860350	HEK293	kidney:	n/a	chr8:67860271-67860280
17	CTCF	chr8:67875020-67875170	HRPEpiC	eye:	n/a	n/a
18	CTCF	chr8:67875130-67875218	GM10266	blood:	n/a	n/a
19	CTCF	chr8:67875016-67875216	GM12891	blood:	n/a	n/a
20	CTCF	chr8:67875120-67875270	GM12873	blood:	n/a	n/a
21	CTCF	chr8:67860120-67860270	HMF	breast:	n/a	n/a
22	CTCF	chr8:67874840-67874990	GM12868	blood:	n/a	n/a
23	CTCF	chr8:67875061-67875258	Fibrobl	skin:	n/a	n/a
24	CTCF	chr8:67875040-67875190	BJ	skin:	n/a	n/a
25	CTCF	chr8:67875100-67875250	NHDF-neo	bronchial:	n/a	n/a
26	CTCF	chr8:67874760-67874910	GM12871	blood:	n/a	n/a
27	CTCF	chr8:67860200-67860350	HPAF	blood vessel:	n/a	chr8:67860271-67860280
28	CTCF	chr8:67875060-67875210	GM12865	blood:	n/a	n/a
29	CTCF	chr8:67875022-67875319	GM12878	blood:	n/a	n/a
30	CTCF	chr8:67875140-67875290	HMF	breast:	n/a	n/a
31	CTCF	chr8:67875060-67875210	HBMEC	blood vessel:	n/a	n/a
32	CTCF	chr8:67875120-67875270	AG09319	gingival:	n/a	n/a
33	CTCF	chr8:67860260-67860410	HCFaa	heart:	n/a	chr8:67860271-67860280
34	CTCF	chr8:67860193-67860432	K562	blood:	n/a	chr8:67860271-67860280
35	CTCF	chr8:67875070-67875206	SK-N-SH_RA	brain:	n/a	n/a
36	CTCF	chr8:67875100-67875250	HPF	lung:	n/a	n/a
37	CTCF	chr8:67860220-67860370	HPF	lung:	n/a	chr8:67860271-67860280
38	CTCF	chr8:67875080-67875230	HRE	kidney:	n/a	n/a
39	CTCF	chr8:67875081-67875241	GM10248	blood:	n/a	n/a
40	CTCF	chr8:67875057-67875235	GM19240	blood:	n/a	n/a
41	CTCF	chr8:67875080-67875230	SAEC	small airway:	n/a	n/a
42	CTCF	chr8:67860180-67860330	AG04450	lung:	n/a	chr8:67860271-67860280
43	CTCF	chr8:67875000-67875150	HMEC	breast:	n/a	n/a
44	CTCF	chr8:67875100-67875250	WERI-Rb-1	eye:	n/a	n/a
45	CTCF	chr8:67875040-67875190	GM12867	blood:	n/a	n/a
46	CTCF	chr8:67860180-67860330	AoAF	blood vessel:	n/a	chr8:67860271-67860280
47	CTCF	chr8:67875103-67875171	Pancreas_OC	pancreas:	n/a	n/a
48	CTCF	chr8:67875049-67875262	NHEK	skin:	n/a	n/a
49	CTCF	chr8:67875020-67875170	BE2_C	brain:	n/a	n/a
50	CTCF	chr8:67875060-67875210	AG09309	skin:	n/a	n/a

(count:916 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:67873476-67873526	NHDF-neo	bronchial:	n/a
2	chr8:67873476-67873526	NHDF-neo	bronchial:	n/a
3	chr8:67875646-67875696	SAEC	small airway:	n/a
4	chr8:67873343-67873393	MCF10A-Er-Src	breast:	n/a
5	chr8:67873799-67873849	Hepatocyte	liver:	n/a
6	chr8:67875646-67875696	T-47D	breast:	n/a
7	chr8:67875441-67875491	ECC-1	luminal epithelium:	n/a
8	chr8:67874178-67874228	MCF10A-Er-Src	breast:	n/a
9	chr8:67872678-67872728	AG04450	lung:	fetal
10	chr8:67875441-67875491	HCF	heart:	n/a
11	chr8:67872678-67872728	SAEC	small airway:	n/a
12	chr8:67874206-67874256	LNCaP	prostate:	n/a
13	chr8:67875033-67875083	AG04449	skin:	fetal
14	chr8:67874206-67874256	HRE	kidney:	n/a
15	chr8:67874206-67874256	NHBE	bronchial:	n/a
16	chr8:67874858-67874908	ECC-1	luminal epithelium:	n/a
17	chr8:67874250-67874300	HAEpiC	amniotic membrane:	n/a
18	chr8:67871302-67871352	PANC-1	pancreas:	n/a
19	chr8:67874206-67874256	IMR90	lung:	fetal
20	chr8:67873799-67873849	GM12892	blood:	n/a
21	chr8:67875441-67875491	SK-N-SH	brain:	n/a
22	chr8:67874858-67874908	BE2_C	brain:	n/a
23	chr8:67872678-67872728	PrEC	prostate:	n/a
24	chr8:67875646-67875696	PrEC	prostate:	n/a
25	chr8:67875261-67875311	HPAEpiC	pulmonary alveolar:	n/a
26	chr8:67874366-67874416	IMR90	lung:	fetal
27	chr8:67874250-67874300	CMK	blood:	n/a
28	chr8:67874250-67874300	T-47D	breast:	n/a
29	chr8:67873476-67873526	MCF-7	breast:	n/a
30	chr8:67873511-67873561	ovcar-3	ovarian:	n/a
31	chr8:67873343-67873393	HEEpiC	esophagus:	n/a
32	chr8:67873511-67873561	HCPEpiC	choroid plexus:	n/a
33	chr8:67874366-67874416	Jurkat	blood:	n/a
34	chr8:67875261-67875311	HCF	heart:	n/a
35	chr8:67873476-67873526	GM19239	blood:	n/a
36	chr8:67875646-67875696	HUVEC	blood vessel:	n/a
37	chr8:67875441-67875491	AG09319	gingival:	n/a
38	chr8:67871302-67871352	PrEC	prostate:	n/a
39	chr8:67872678-67872728	ovcar-3	ovarian:	n/a
40	chr8:67875646-67875696	Hela-S3	cervix:	n/a
41	chr8:67872678-67872728	MCF-7	breast:	n/a
42	chr8:67874178-67874228	SK-N-SH_RA	brain:	n/a
43	chr8:67873476-67873526	RPTEC	kidney:	n/a
44	chr8:67874858-67874908	Jurkat	blood:	n/a
45	chr8:67873799-67873849	SAEC	small airway:	n/a
46	chr8:67874366-67874416	CMK	blood:	n/a
47	chr8:67874178-67874228	K562	blood:	n/a
48	chr8:67875646-67875696	AG10803	skin:	n/a
49	chr8:67873343-67873393	A549	lung:	n/a
50	chr8:67874206-67874256	PrEC	prostate:	n/a

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:67852702..67855011-chr8:67858624..67860729,2	MCF-7	breast:
2	chr8:67867527..67869125-chr8:67873493..67876349,2	K562	blood:
3	chr8:67836559..67839437-chr8:67866045..67867764,2	MCF-7	breast:
4	chr8:67837676..67839511-chr8:67865946..67868529,3	K562	blood:
5	chr8:67871881..67874797-chr8:67902820..67904846,2	K562	blood:
6	chr8:67871185..67874055-chr8:67897952..67900238,2	MCF-7	breast:
7	chr8:67831398..67837310-chr8:67870905..67874577,7	K562	blood:
8	chr8:67860134..67861923-chr8:67868445..67870550,2	MCF-7	breast:
9	chr8:67860134..67861923-chr8:67868445..67870550,2	MCF-7	breast:
10	chr8:67866883..67869231-chr8:67974274..67977139,2	K562	blood:
11	chr8:67853180..67856810-chr8:67857491..67860869,3	K562	blood:
12	chr8:67854974..67857911-chr8:67859030..67861749,2	K562	blood:
13	chr8:67833581..67837805-chr8:67872332..67874822,5	K562	blood:
14	chr8:67866384..67868966-chr8:67875878..67877535,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TCF24-1	chr8:67876334-67876569	NONHSAT127062
2	lnc-TCF24-1	chr8:67876338-67876569	NONHSAT127064

No data

Variant related genes	Relation type
TCF24	TF binding region
TCF24	CpG island
ENSG00000245910	chromatin interactions
ENSG00000121022	chromatin interactions
ENSG00000261787	chromatin interactions
ENSG00000104218	chromatin interactions
ENSG00000254341	chromatin interactions
ENSG00000253223	chromatin interactions

Extended variants
information (count: 278 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:278 , 50 per page) page: 1 2 3 4 5 6

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs200824670	chr8:67865950-67865951	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs370627899	chr8:67866005-67866006	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs374024767	chr8:67866027-67866028	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs374949543	chr8:67866064-67866065	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs201671528	chr8:67866123-67866124	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs201020483	chr8:67866150-67866151	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs201713511	chr8:67866154-67866155	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs199850788	chr8:67866169-67866170	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs367917616	chr8:67866234-67866235	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs370250507	chr8:67866242-67866243	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs374463945	chr8:67866246-67866247	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs199574779	chr8:67866253-67866254	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs200740393	chr8:67866286-67866287	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs367632121	chr8:67866290-67866291	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs372956626	chr8:67866295-67866296	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs550825233	chr8:67866362-67866363	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs570648014	chr8:67866370-67866371	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs547634179	chr8:67866429-67866430	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs565845014	chr8:67866450-67866451	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs536198054	chr8:67866467-67866468	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs185838572	chr8:67866474-67866475	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs542570111	chr8:67866485-67866486	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs369917650	chr8:67866486-67866487	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs566730146	chr8:67866506-67866507	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs535495698	chr8:67866515-67866516	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs552690360	chr8:67866519-67866520	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs368523092	chr8:67866614-67866615	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs555702205	chr8:67866683-67866684	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs569277630	chr8:67866691-67866692	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs372425394	chr8:67866703-67866704	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs557970467	chr8:67866717-67866718	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs202046843	chr8:67866718-67866719	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs554055096	chr8:67866738-67866739	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs199829953	chr8:67866751-67866752	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs368365467	chr8:67866790-67866791	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs541483115	chr8:67866847-67866848	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs62513076	chr8:67866872-67866873	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs561705813	chr8:67866937-67866938	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs530557421	chr8:67866943-67866944	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs544317047	chr8:67866986-67866987	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs190213355	chr8:67867003-67867004	Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs180886664	chr8:67867028-67867029	Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs546780845	chr8:67867029-67867030	Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs185918476	chr8:67867038-67867039	Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs192014892	chr8:67867049-67867050	Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs561019275	chr8:67867054-67867055	Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs549143011	chr8:67867055-67867056	Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs569225845	chr8:67867061-67867062	Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs558806991	chr8:67867062-67867063	Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs371997611	chr8:67867075-67867076	Active TSS	Chromatin interactive region	3 gene(s)	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
Hodgkin''s lymphoma	17606441	CNVD
Seminomas	18059402	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	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
primary effusion lymphomas	17116491	CNVD
Esophageal cancer	20955586	CNVD
Multiple myeloma	16461302	CNVD
abnormal development	18461090	CNVD
Cancer	20164920	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
Salivary gland tumor	18059337	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
Acute myeloid leukemia	21251322	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
Colorectal cancer	16272173	CNVD
Melanoma	22183965	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
low-grade B-cell lymphoma tumor	18367492	CNVD
small cell lung cancer	20016488	CNVD
Sezary syndrome	18413736	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	17142309	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD
Glioblastoma multiforme	19115005	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:448 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:67867000-67867400	Active TSS	ES-WA7 Cell Line	embryonic stem cell
2	chr8:67867200-67867400	Enhancers	Left Ventricle	heart
3	chr8:67867200-67867400	Active TSS	Hela-S3	cervix
4	chr8:67867200-67867400	Active TSS	HepG2	liver
5	chr8:67867200-67867400	Active TSS	K562	blood
6	chr8:67867200-67867600	Active TSS	A549	lung
7	chr8:67867200-67868600	Enhancers	Skeletal Muscle Female	skeletal muscle
8	chr8:67867200-67869000	Enhancers	Fetal Heart	heart
9	chr8:67867400-67867800	Flanking Active TSS	Hela-S3	cervix
10	chr8:67867400-67867800	Flanking Active TSS	HepG2	liver
11	chr8:67867400-67867800	Flanking Active TSS	K562	blood
12	chr8:67867400-67868000	Enhancers	Skeletal Muscle Male	skeletal muscle
13	chr8:67867600-67867800	Enhancers	Stomach Mucosa	stomach
14	chr8:67867600-67867800	Flanking Active TSS	A549	lung
15	chr8:67867800-67868000	Enhancers	Duodenum Smooth Muscle	Duodenum
16	chr8:67867800-67868000	Enhancers	HepG2	liver
17	chr8:67867800-67868000	Enhancers	K562	blood
18	chr8:67868200-67868600	Enhancers	Psoas Muscle	Psoas
19	chr8:67870600-67870800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
20	chr8:67871400-67871600	Bivalent Enhancer	Dnd41	blood
21	chr8:67872800-67873000	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
22	chr8:67872800-67873200	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
23	chr8:67872800-67874400	Active TSS	Pancreatic Islets	Pancreatic Islet
24	chr8:67873000-67873400	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell
25	chr8:67873000-67876200	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
26	chr8:67873000-67876400	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
27	chr8:67873200-67873400	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
28	chr8:67873200-67873400	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
29	chr8:67873200-67873400	Bivalent/Poised TSS	iPS DF 6.9 Cell Line	embryonic stem cell
30	chr8:67873200-67873400	Bivalent/Poised TSS	iPS DF 19.11 Cell Line	embryonic stem cell
31	chr8:67873200-67873400	Bivalent/Poised TSS	Primary T cells from cord blood	blood
32	chr8:67873200-67873400	Bivalent Enhancer	Primary hematopoietic stem cells	blood
33	chr8:67873200-67873400	Bivalent Enhancer	Primary hematopoietic stem cells short term culture	blood
34	chr8:67873200-67873400	Bivalent Enhancer	Primary T cells effector/memory enriched fromperipheralblood	blood
35	chr8:67873200-67873400	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
36	chr8:67873200-67873400	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr8:67873200-67873400	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr8:67873200-67873400	Bivalent Enhancer	Fetal Brain Female	brain
39	chr8:67873200-67873400	Active TSS	Right Atrium	heart
40	chr8:67873200-67873400	Bivalent Enhancer	A549	lung
41	chr8:67873200-67873600	Bivalent Enhancer	Primary T helper 17 cells PMA-I stimulated	--
42	chr8:67873200-67873600	Bivalent Enhancer	Primary T helper cells fromperipheralblood	blood
43	chr8:67873200-67873600	Bivalent Enhancer	Fetal Brain Male	brain
44	chr8:67873200-67874000	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
45	chr8:67873200-67874000	Bivalent Enhancer	Primary T helper memory cells from peripheral blood 1	blood
46	chr8:67873200-67874000	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
47	chr8:67873200-67874000	Bivalent/Poised TSS	Ganglion Eminence derived primary cultured neurospheres	brain
48	chr8:67873200-67874200	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
49	chr8:67873200-67874400	Bivalent/Poised TSS	Left Ventricle	heart
50	chr8:67873200-67875600	Bivalent/Poised TSS	ES-UCSF4 Cell Line	embryonic stem cell

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