Variant report

Variant	esv1805280
Chromosome Location	chr7:64582661-64634920
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:318)
CpG islands
(count:245)
Chromatin interactive
region (count:0)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:318 , 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	ARID3A	chr7:64606224-64606235	HepG2	liver:	n/a	n/a
2	BATF	chr7:64607889-64608098	GM12878	blood:	n/a	n/a
3	BATF	chr7:64583217-64583436	GM12878	blood:	n/a	chr7:64583312-64583322
4	BATF	chr7:64626662-64626865	GM12878	blood:	n/a	chr7:64626758-64626769
5	BCL11A	chr7:64593480-64593764	GM12878	blood:	n/a	n/a
6	CBX3	chr7:64610511-64610893	K562	blood:	n/a	n/a
7	CBX3	chr7:64600836-64601564	K562	blood:	n/a	n/a
8	CBX3	chr7:64596961-64597693	K562	blood:	n/a	n/a
9	CBX3	chr7:64596910-64598009	K562	blood:	n/a	n/a
10	CEBPB	chr7:64606211-64606264	Hela-S3	cervix:	n/a	n/a
11	CEBPB	chr7:64605524-64605561	IMR90	lung:	n/a	n/a
12	CEBPB	chr7:64606056-64606680	HepG2	liver:	n/a	chr7:64606200-64606211
13	CEBPB	chr7:64606046-64606267	K562	blood:	n/a	chr7:64606200-64606211
14	CEBPB	chr7:64605904-64606366	K562	blood:	n/a	chr7:64606200-64606211
15	CEBPB	chr7:64604687-64604747	K562	blood:	n/a	n/a
16	CEBPB	chr7:64605885-64607095	A549	lung:	n/a	chr7:64606200-64606211
17	CEBPB	chr7:64606408-64607212	K562	blood:	n/a	n/a
18	CEBPB	chr7:64606032-64607102	IMR90	lung:	n/a	chr7:64606200-64606211
19	CEBPB	chr7:64604592-64604811	IMR90	lung:	n/a	chr7:64604747-64604758
20	CEBPB	chr7:64597188-64597656	K562	blood:	n/a	n/a
21	CEBPB	chr7:64604715-64604798	Hela-S3	cervix:	n/a	chr7:64604747-64604758
22	CEBPB	chr7:64590987-64591374	K562	blood:	n/a	chr7:64591197-64591210 chr7:64591161-64591173
23	CEBPB	chr7:64604592-64605626	A549	lung:	n/a	chr7:64605174-64605185 chr7:64604747-64604758
24	CEBPB	chr7:64605151-64605345	HepG2	liver:	n/a	chr7:64605174-64605185
25	CEBPB	chr7:64604492-64605803	K562	blood:	n/a	chr7:64605174-64605185 chr7:64604747-64604758
26	CEBPB	chr7:64605088-64605299	IMR90	lung:	n/a	chr7:64605174-64605185
27	CEBPB	chr7:64606894-64606926	K562	blood:	n/a	n/a
28	CEBPB	chr7:64604706-64604728	HepG2	liver:	n/a	n/a
29	CEBPD	chr7:64610399-64610967	K562	blood:	n/a	n/a
30	CEBPD	chr7:64597188-64597607	K562	blood:	n/a	n/a
31	CTCF	chr7:64593534-64593772	A549	lung:	n/a	n/a
32	CTCF	chr7:64593565-64593672	GM13976	blood:	n/a	n/a
33	CTCF	chr7:64593457-64593659	K562	blood:	n/a	n/a
34	CTCF	chr7:64593609-64593644	MCF-7	breast:	n/a	n/a
35	CTCF	chr7:64593500-64593650	HMEC	breast:	n/a	n/a
36	CTCF	chr7:64585135-64585241	Medullo	brain:	n/a	chr7:64585182-64585203 chr7:64585180-64585198
37	CTCF	chr7:64585340-64585429	GM20000	blood:	n/a	n/a
38	CTCF	chr7:64592615-64592665	Pancreas_OC	pancreas:	n/a	n/a
39	CTCF	chr7:64593405-64593802	A549	lung:	n/a	n/a
40	CTCF	chr7:64593500-64593650	HEEpiC	esophagus:	n/a	n/a
41	CTCF	chr7:64593560-64593710	NB4	blood:	n/a	n/a
42	CTCF	chr7:64593587-64593656	Pancreas_OC	pancreas:	n/a	n/a
43	CTCF	chr7:64593520-64593670	HMEC	breast:	n/a	n/a
44	CTCF	chr7:64593520-64593670	MCF-7	breast:	n/a	n/a
45	CTCF	chr7:64593567-64593658	MCF-7	breast:	n/a	n/a
46	CTCF	chr7:64593578-64593734	Lung_OC	lung:	n/a	n/a
47	CTCF	chr7:64593520-64593670	BE2_C	brain:	n/a	n/a
48	CTCF	chr7:64593500-64593650	HRPEpiC	eye:	n/a	n/a
49	CTCF	chr7:64593401-64593854	K562	blood:	n/a	n/a
50	CTCF	chr7:64593526-64593700	GM10248	blood:	n/a	n/a

(count:245 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:64597604-64597654	HepG2	liver:	n/a
2	chr7:64597604-64597654	HepG2	liver:	n/a
3	chr7:64602752-64602802	HCPEpiC	choroid plexus:	n/a
4	chr7:64597604-64597654	GM06990	blood:	n/a
5	chr7:64601662-64601712	NHBE	bronchial:	n/a
6	chr7:64602752-64602802	ovcar-3	ovarian:	n/a
7	chr7:64587587-64587637	HCT-116	colon:	n/a
8	chr7:64587587-64587637	HNPCEpiC	eye:	n/a
9	chr7:64587587-64587637	HPAEpiC	pulmonary alveolar:	n/a
10	chr7:64587587-64587637	HIPEpiC	eye:	n/a
11	chr7:64601662-64601712	AG09309	skin:	n/a
12	chr7:64601662-64601712	Jurkat	blood:	n/a
13	chr7:64601662-64601712	AG04450	lung:	fetal
14	chr7:64601662-64601712	HCPEpiC	choroid plexus:	n/a
15	chr7:64602752-64602802	GM12878	blood:	n/a
16	chr7:64597604-64597654	HCM	heart:	n/a
17	chr7:64597604-64597654	AG10803	skin:	n/a
18	chr7:64601662-64601712	GM12892	blood:	n/a
19	chr7:64601662-64601712	HMEC	breast:	n/a
20	chr7:64601662-64601712	HRE	kidney:	n/a
21	chr7:64602752-64602802	NH-A	brain:	n/a
22	chr7:64601662-64601712	Hela-S3	cervix:	n/a
23	chr7:64601662-64601712	HCM	heart:	n/a
24	chr7:64601662-64601712	ECC-1	luminal epithelium:	n/a
25	chr7:64601662-64601712	NH-A	brain:	n/a
26	chr7:64587587-64587637	Hepatocyte	liver:	n/a
27	chr7:64602752-64602802	IMR90	lung:	fetal
28	chr7:64601662-64601712	MCF10A-Er-Src	breast:	n/a
29	chr7:64601662-64601712	PANC-1	pancreas:	n/a
30	chr7:64587587-64587637	T-47D	breast:	n/a
31	chr7:64587587-64587637	AoSMC	blood vessel:	n/a
32	chr7:64587587-64587637	ECC-1	luminal epithelium:	n/a
33	chr7:64597604-64597654	HRCEpiC	kidney:	n/a
34	chr7:64597604-64597654	SK-N-SH	brain:	n/a
35	chr7:64601662-64601712	Hepatocyte	liver:	n/a
36	chr7:64587587-64587637	AG09319	gingival:	n/a
37	chr7:64602752-64602802	AG04450	lung:	fetal
38	chr7:64597604-64597654	Caco-2	colon:	n/a
39	chr7:64602752-64602802	Hepatocyte	liver:	n/a
40	chr7:64587587-64587637	GM12892	blood:	n/a
41	chr7:64587587-64587637	HCPEpiC	choroid plexus:	n/a
42	chr7:64597604-64597654	RPTEC	kidney:	n/a
43	chr7:64597604-64597654	T-47D	breast:	n/a
44	chr7:64601662-64601712	ProgFib	skin:	n/a
45	chr7:64601662-64601712	GM06990	blood:	n/a
46	chr7:64597604-64597654	MCF-7	breast:	n/a
47	chr7:64597604-64597654	PFSK-1	brain:	n/a
48	chr7:64601662-64601712	PrEC	prostate:	n/a
49	chr7:64587587-64587637	HAEpiC	amniotic membrane:	n/a
50	chr7:64597604-64597654	HMEC	breast:	n/a

No data

Variant related genes	Relation type
INTS4L1	TF binding region
INTS4L1	CpG island

Extended variants
information (count: 68 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:68 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs62455030	chr7:64596820-64596821	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs62455031	chr7:64597122-64597123	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs62455032	chr7:64597405-64597406	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs535653050	chr7:64597464-64597465	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs1709521	chr7:64597546-64597547	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs2140593	chr7:64597624-64597625	Inactive region	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
7	rs534954477	chr7:64597683-64597684	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs558064133	chr7:64597800-64597801	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs577590077	chr7:64597802-64597803	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs543373654	chr7:64598194-64598195	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs1852022	chr7:64598235-64598236	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs550909593	chr7:64599770-64599771	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs545292279	chr7:64599882-64599883	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs373170395	chr7:64599890-64599891	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs189566333	chr7:64599895-64599896	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs2458804	chr7:64599912-64599913	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs536787131	chr7:64599935-64599936	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs547103420	chr7:64599956-64599957	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs565912731	chr7:64599969-64599970	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs534784786	chr7:64600024-64600025	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs557785080	chr7:64600054-64600055	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs565089355	chr7:64600058-64600059	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs577828690	chr7:64600071-64600072	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs369990956	chr7:64600095-64600096	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs372403278	chr7:64600099-64600100	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs536647120	chr7:64600171-64600172	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs552628513	chr7:64601104-64601105	Active TSS Bivalent/Poised TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs573121401	chr7:64601134-64601135	Active TSS Bivalent/Poised TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs545160892	chr7:64601145-64601146	Active TSS Bivalent/Poised TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs375114812	chr7:64601258-64601259	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs369473769	chr7:64601260-64601261	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs565446621	chr7:64601276-64601277	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs531185471	chr7:64601340-64601341	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs190224688	chr7:64601374-64601375	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs146473372	chr7:64601414-64601415	Bivalent/Poised TSS Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs561371215	chr7:64601451-64601452	Bivalent/Poised TSS Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs181286047	chr7:64601522-64601523	Bivalent/Poised TSS Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs72504867	chr7:64601548-64601549	Bivalent/Poised TSS Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs186335692	chr7:64601564-64601565	Bivalent/Poised TSS Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs75249977	chr7:64601570-64601571	Bivalent/Poised TSS Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs143357318	chr7:64601579-64601580	Bivalent/Poised TSS Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs200287937	chr7:64601585-64601586	Bivalent/Poised TSS Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs532689861	chr7:64601598-64601599	Bivalent/Poised TSS Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs376553931	chr7:64601601-64601602	Bivalent/Poised TSS Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs370067068	chr7:64601602-64601603	Bivalent/Poised TSS Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs528305087	chr7:64601604-64601605	Bivalent/Poised TSS Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs140931305	chr7:64601606-64601607	Bivalent/Poised TSS Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs374380452	chr7:64601652-64601653	Bivalent/Poised TSS Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
49	rs2690473	chr7:64601679-64601680	Bivalent/Poised TSS Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
50	rs370812304	chr7:64601730-64601731	Bivalent/Poised TSS Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:82)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17170743	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Follicular lymphoma	20505157	CNVD
Biliary cancer	19435499	CNVD
Williams-beuren syndrome	22470819	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21750150	CNVD
Cancer	21183584	CNVD
Hepatocellular carcinoma	16750200	CNVD
Non-small cell lung cancer	21829676	CNVD
Gastric cancer	24379144	CNVD
Glioblastoma multiforme	17002787	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	16864856	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Squamous cell cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	17387387	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Oligodendroglial tumors	17285580	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Shwachman-Diamond syndrome	22934832	CNVD
Glioblastoma	21080181	CNVD
Colorectal cancer	19359472	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Leukemia	17361228	CNVD
Breast cancer	16461572	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Malignant melanoma	17690212	CNVD
Breast cancer	21990379	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	21399695	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Astrocytoma	22246337	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Acute monocytic leukemia	16498392	CNVD
Prostate cancer	16461572	CNVD
Salivary gland tumor	18059337	CNVD
Multiple myeloma	17550852	CNVD
Acute myeloid leukemia	21251322	CNVD
small cell lung cancer	20016488	CNVD
Bladder cancer	21909424	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
small cell lung cancer	17426248	CNVD
Cognitive impairment	21505072	CNVD
Schizophrenia	20967226	CNVD
Cancer	21272361	CNVD
Hodgkin''s lymphoma	17606441	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:81 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:64600000-64600200	Enhancers	Brain Hippocampus Middle	brain
2	chr7:64601000-64601200	Active TSS	ES-I3 Cell Line	embryonic stem cell
3	chr7:64601000-64601200	Bivalent/Poised TSS	Primary T cells fromperipheralblood	blood
4	chr7:64601000-64601200	Bivalent/Poised TSS	Fetal Muscle Trunk	muscle
5	chr7:64601000-64601400	Active TSS	Primary B cells from peripheral blood	blood
6	chr7:64601000-64601400	Bivalent/Poised TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr7:64601000-64601400	Active TSS	Pancreatic Islets	Pancreatic Islet
8	chr7:64601000-64601400	Active TSS	Placenta	Placenta
9	chr7:64601000-64601400	Active TSS	Right Atrium	heart
10	chr7:64601000-64601400	Bivalent/Poised TSS	HMEC	breast
11	chr7:64601000-64601600	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr7:64601000-64601600	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr7:64601000-64601600	Active TSS	Adipose Nuclei	Adipose
14	chr7:64601000-64601600	Active TSS	Ovary	ovary
15	chr7:64601000-64601800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
16	chr7:64601000-64601800	Active TSS	Cortex derived primary cultured neurospheres	brain
17	chr7:64601000-64601800	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
18	chr7:64601000-64601800	Bivalent/Poised TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr7:64601000-64601800	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
20	chr7:64601000-64601800	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr7:64601000-64601800	Active TSS	Duodenum Smooth Muscle	Duodenum
22	chr7:64601000-64601800	Active TSS	Fetal Brain Female	brain
23	chr7:64601000-64601800	Bivalent/Poised TSS	Fetal Stomach	stomach
24	chr7:64601000-64601800	Active TSS	Psoas Muscle	Psoas
25	chr7:64601000-64601800	Active TSS	Right Ventricle	heart
26	chr7:64601000-64601800	Active TSS	HSMM	muscle
27	chr7:64601000-64601800	Active TSS	HSMMtube	muscle
28	chr7:64601000-64602000	Active TSS	H9 Cell Line	embryonic stem cell
29	chr7:64601000-64602000	Active TSS	iPS-15b Cell Line	embryonic stem cell
30	chr7:64601000-64602000	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
31	chr7:64601000-64602000	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
32	chr7:64601000-64602000	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr7:64601000-64602000	Active TSS	Brain Anterior Caudate	brain
34	chr7:64601000-64602000	Active TSS	Brain Germinal Matrix	brain
35	chr7:64601000-64602000	Active TSS	Brain Hippocampus Middle	brain
36	chr7:64601000-64602000	Bivalent/Poised TSS	Fetal Adrenal Gland	Adrenal Gland
37	chr7:64601000-64602000	Active TSS	K562	blood
38	chr7:64601200-64601400	Flanking Bivalent TSS/Enh	Primary T cells fromperipheralblood	blood
39	chr7:64601200-64601400	Flanking Bivalent TSS/Enh	Primary T regulatory cells fromperipheralblood	blood
40	chr7:64601200-64601400	Enhancers	Colonic Mucosa	Colon
41	chr7:64601200-64601600	Active TSS	H1 Cell Line	embryonic stem cell
42	chr7:64601200-64601600	Bivalent/Poised TSS	IMR90 fetal lung fibroblasts Cell Line	lung
43	chr7:64601200-64601600	Active TSS	Breast Myoepithelial Primary Cells	Breast
44	chr7:64601200-64601600	Active TSS	Osteobl	bone
45	chr7:64601200-64601800	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
46	chr7:64601200-64601800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
47	chr7:64601200-64601800	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
48	chr7:64601200-64601800	Active TSS	Stomach Smooth Muscle	stomach
49	chr7:64601200-64601800	Active TSS	HUVEC	blood vessel
50	chr7:64601200-64602000	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell

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