Variant report

Variant	esv21367
Chromosome Location	chr7:64328624-64345129
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	chr7:64339145-64339494	HepG2	liver:	n/a	n/a
2	BHLHE40	chr7:64339142-64339479	K562	blood:	n/a	n/a
3	CEBPB	chr7:64328627-64328684	K562	blood:	n/a	chr7:64328659-64328670 chr7:64328659-64328668
4	CEBPB	chr7:64328901-64329071	K562	blood:	n/a	chr7:64329035-64329046
5	CEBPB	chr7:64331483-64331670	HepG2	liver:	n/a	chr7:64331519-64331530 chr7:64331519-64331528 chr7:64331517-64331528 chr7:64331517-64331530
6	CEBPB	chr7:64342772-64343080	IMR90	lung:	n/a	n/a
7	CEBPB	chr7:64331481-64331626	K562	blood:	n/a	chr7:64331519-64331530 chr7:64331519-64331528 chr7:64331517-64331528 chr7:64331517-64331530
8	CEBPB	chr7:64328537-64328820	HepG2	liver:	n/a	chr7:64328659-64328670 chr7:64328659-64328668
9	CHD2	chr7:64337839-64337927	HepG2	liver:	n/a	n/a
10	CHD2	chr7:64339217-64339295	K562	blood:	n/a	n/a
11	CTCF	chr7:64329626-64329723	K562	blood:	n/a	n/a
12	CTCF	chr7:64342629-64342746	H1-hESC	embryonic stem cell:	n/a	n/a
13	CTCF	chr7:64339818-64339865	Spleen_OC	spleen:	n/a	n/a
14	CTCF	chr7:64329574-64329792	K562	blood:	n/a	n/a
15	CTCF	chr7:64329600-64329718	HepG2	liver:	n/a	n/a
16	E2F6	chr7:64342778-64343067	H1-hESC	embryonic stem cell:	n/a	n/a
17	EGR1	chr7:64328865-64329138	K562	blood:	n/a	chr7:64329014-64329029 chr7:64329015-64329028 chr7:64329015-64329028 chr7:64329010-64329032 chr7:64329015-64329028 chr7:64329016-64329025 chr7:64329016-64329027 chr7:64329016-64329026 chr7:64329014-64329028
18	EGR1	chr7:64328901-64329159	K562	blood:	n/a	chr7:64329014-64329029 chr7:64329015-64329028 chr7:64329015-64329028 chr7:64329010-64329032 chr7:64329015-64329028 chr7:64329016-64329025 chr7:64329016-64329027 chr7:64329016-64329026 chr7:64329014-64329028
19	FOS	chr7:64338998-64339465	HUVEC	blood vessel:	n/a	chr7:64339286-64339294 chr7:64339286-64339293 chr7:64339285-64339295 chr7:64339284-64339295
20	FOSL2	chr7:64339069-64339482	HepG2	liver:	n/a	chr7:64339286-64339294 chr7:64339286-64339293 chr7:64339285-64339295
21	JUN	chr7:64339208-64339408	HepG2	liver:	n/a	chr7:64339286-64339294 chr7:64339286-64339293 chr7:64339285-64339295
22	JUN	chr7:64339006-64339601	K562	blood:	n/a	chr7:64339286-64339294 chr7:64339286-64339293 chr7:64339285-64339295
23	JUND	chr7:64339209-64339441	K562	blood:	n/a	chr7:64339286-64339294 chr7:64339286-64339293 chr7:64339284-64339295 chr7:64339285-64339295
24	JUND	chr7:64340571-64340687	H1-hESC	embryonic stem cell:	n/a	n/a
25	JUND	chr7:64335473-64335665	HepG2	liver:	n/a	chr7:64335533-64335544
26	JUND	chr7:64339106-64339457	HepG2	liver:	n/a	chr7:64339286-64339294 chr7:64339286-64339293 chr7:64339284-64339295 chr7:64339285-64339295
27	MAFK	chr7:64339326-64339480	K562	blood:	n/a	n/a
28	MAX	chr7:64342742-64343063	H1-hESC	embryonic stem cell:	n/a	n/a
29	MAX	chr7:64339274-64339405	HepG2	liver:	n/a	chr7:64339285-64339294 chr7:64339286-64339295
30	MXI1	chr7:64337369-64338620	SK-N-SH	brain:	n/a	n/a
31	MXI1	chr7:64342942-64342983	GM12878	blood:	n/a	n/a
32	MXI1	chr7:64337852-64338063	H1-hESC	embryonic stem cell:	n/a	n/a
33	MYC	chr7:64343886-64343973	H1-hESC	embryonic stem cell:	n/a	n/a
34	MYC	chr7:64330467-64330498	MCF-7	breast:	n/a	n/a
35	NFIC	chr7:64334391-64334930	SK-N-SH	brain:	n/a	n/a
36	NFIC	chr7:64334291-64334969	SK-N-SH	brain:	n/a	n/a
37	NRF1	chr7:64337798-64338017	GM12878	blood:	n/a	n/a
38	NRF1	chr7:64342756-64342959	H1-hESC	embryonic stem cell:	n/a	n/a
39	NRF1	chr7:64337566-64338274	SK-N-SH	brain:	n/a	n/a
40	NRF1	chr7:64337757-64338107	H1-hESC	embryonic stem cell:	n/a	n/a
41	NRF1	chr7:64342747-64342993	GM12878	blood:	n/a	n/a
42	POLR2A	chr7:64337614-64338208	H1-neurons	neurons:	n/a	n/a
43	POLR2A	chr7:64337680-64338083	H1-neurons	neurons:	n/a	n/a
44	RAD21	chr7:64329568-64329746	HepG2	liver:	n/a	n/a
45	SETDB1	chr7:64342812-64343532	K562	blood:	n/a	n/a
46	SIN3A	chr7:64342736-64342976	H1-hESC	embryonic stem cell:	n/a	n/a
47	SIN3A	chr7:64337818-64338171	H1-hESC	embryonic stem cell:	n/a	n/a
48	TCF7L2	chr7:64336966-64337130	Hela-S3	cervix:	n/a	n/a
49	YY1	chr7:64337765-64338173	SK-N-SH_RA	brain:	n/a	n/a
50	YY1	chr7:64337867-64338202	SK-N-SH_RA	brain:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:64337958-64338008	A549	lung:	n/a
2	chr7:64328890-64328940	HCF	heart:	n/a
3	chr7:64337958-64338008	A549	lung:	n/a
4	chr7:64328890-64328940	HCF	heart:	n/a
5	chr7:64328890-64328940	ECC-1	luminal epithelium:	n/a
6	chr7:64340804-64340854	PFSK-1	brain:	n/a
7	chr7:64335660-64335710	HCM	heart:	n/a
8	chr7:64337958-64338008	PANC-1	pancreas:	n/a
9	chr7:64333138-64333188	A549	lung:	n/a
10	chr7:64341459-64341509	HRPEpiC	eye:	n/a
11	chr7:64335660-64335710	CMK	blood:	n/a
12	chr7:64338366-64338416	HNPCEpiC	eye:	n/a
13	chr7:64332970-64333020	Hela-S3	cervix:	n/a
14	chr7:64330819-64330869	PANC-1	pancreas:	n/a
15	chr7:64328715-64328765	GM12891	blood:	n/a
16	chr7:64336120-64336170	Hela-S3	cervix:	n/a
17	chr7:64330493-64330543	GM12878	blood:	n/a
18	chr7:64337958-64338008	GM12892	blood:	n/a
19	chr7:64336329-64336379	HL-60	blood:	n/a
20	chr7:64340804-64340854	K562	blood:	n/a
21	chr7:64330819-64330869	H1-hESC	embryonic stem cell:	embryo
22	chr7:64336709-64336759	SK-N-SH	brain:	n/a
23	chr7:64332970-64333020	MCF-7	breast:	n/a
24	chr7:64337958-64338008	HRE	kidney:	n/a
25	chr7:64328890-64328940	K562	blood:	n/a
26	chr7:64343315-64343365	AG04449	skin:	fetal
27	chr7:64342997-64343047	NHBE	bronchial:	n/a
28	chr7:64328759-64328809	HEK293	kidney:	embryo
29	chr7:64341459-64341509	AG10803	skin:	n/a
30	chr7:64336709-64336759	GM12878	blood:	n/a
31	chr7:64340804-64340854	HCPEpiC	choroid plexus:	n/a
32	chr7:64340804-64340854	AG10803	skin:	n/a
33	chr7:64333138-64333188	SK-N-SH_RA	brain:	n/a
34	chr7:64333138-64333188	HNPCEpiC	eye:	n/a
35	chr7:64340804-64340854	HCT-116	colon:	n/a
36	chr7:64336120-64336170	Caco-2	colon:	n/a
37	chr7:64336120-64336170	HEK293	kidney:	embryo
38	chr7:64338366-64338416	SK-N-SH	brain:	n/a
39	chr7:64343315-64343365	LNCaP	prostate:	n/a
40	chr7:64342484-64342534	Caco-2	colon:	n/a
41	chr7:64328715-64328765	SK-N-SH	brain:	n/a
42	chr7:64336709-64336759	U87	brain:	n/a
43	chr7:64338366-64338416	MCF10A-Er-Src	breast:	n/a
44	chr7:64336709-64336759	HUVEC	blood vessel:	n/a
45	chr7:64330785-64330835	Caco-2	colon:	n/a
46	chr7:64335660-64335710	GM12891	blood:	n/a
47	chr7:64338366-64338416	PANC-1	pancreas:	n/a
48	chr7:64338366-64338416	GM19239	blood:	n/a
49	chr7:64335660-64335710	HCT-116	colon:	n/a
50	chr7:64330493-64330543	U87	brain:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:64279288..64281890-chr7:64330728..64333197,2	MCF-7	breast:
2	chr7:64340851..64342606-chr7:64346677..64349017,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF117-3	chr7:64327248-64328970	NONHSAT121045
2	lnc-ZNF138-1	chr7:64338163-64338208	XLOC_006130
3	lnc-ZNF138-1	chr7:64338759-64338873	NONHSAT121048
4	lnc-ZNF117-3	chr7:64330245-64330355	NONHSAT121045
5	lnc-ZNF117-3	chr7:64327248-64328970	NONHSAT121046
6	lnc-ZNF138-1	chr7:64339828-64340136	XLOC_006130
7	lnc-ZNF117-3	chr7:64335204-64335354	NONHSAT121046
8	lnc-ZNF138-1	chr7:64339828-64340109	NONHSAT121048
9	lnc-ZNF138-1	chr7:64338038-64338252	NONHSAT121048

Variant related genes	Relation type
ZNF273	TF binding region
ZNF273	CpG island

Extended variants
information (count: 621 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:621 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs143981035	chr7:64328668-64328669	Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
2	rs192866581	chr7:64328706-64328707	Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
3	rs147310938	chr7:64328709-64328710	Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
4	rs546279003	chr7:64328719-64328720	Weak transcription	TF binding region CpG island lncRNA	1 gene(s)	Overlapped CNVs	n/a
5	rs77396282	chr7:64328722-64328723	Weak transcription	TF binding region CpG island lncRNA	1 gene(s)	Overlapped CNVs	n/a
6	rs4718150	chr7:64328759-64328760	Weak transcription	TF binding region CpG island lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs4718151	chr7:64328764-64328765	Weak transcription	TF binding region CpG island lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
8	rs115625389	chr7:64328794-64328795	Weak transcription	TF binding region CpG island lncRNA	1 gene(s)	Overlapped CNVs	n/a
9	rs538091348	chr7:64328808-64328809	Weak transcription	TF binding region CpG island lncRNA	1 gene(s)	Overlapped CNVs	n/a
10	rs554842259	chr7:64328813-64328814	Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
11	rs557044943	chr7:64328853-64328854	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
12	rs111572601	chr7:64328855-64328856	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
13	rs575037029	chr7:64328915-64328916	Weak transcription	TF binding region CpG island lncRNA	1 gene(s)	Overlapped CNVs	n/a
14	rs575275926	chr7:64328919-64328920	Weak transcription	TF binding region CpG island lncRNA	1 gene(s)	Overlapped CNVs	n/a
15	rs553895263	chr7:64328924-64328925	Weak transcription	TF binding region CpG island lncRNA	1 gene(s)	Overlapped CNVs	n/a
16	rs111607321	chr7:64328937-64328938	Weak transcription	TF binding region CpG island lncRNA	1 gene(s)	Overlapped CNVs	n/a
17	rs546296755	chr7:64328960-64328961	Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
18	rs184986791	chr7:64329019-64329020	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs142435460	chr7:64329036-64329037	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs375014875	chr7:64329070-64329071	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs539779492	chr7:64329092-64329093	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs529951613	chr7:64329098-64329099	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs546539080	chr7:64329147-64329148	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs546992419	chr7:64329150-64329151	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs545890827	chr7:64329156-64329157	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs559913249	chr7:64329157-64329158	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs369416581	chr7:64329205-64329206	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs373196614	chr7:64329226-64329227	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs35021223	chr7:64329231-64329232	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs532016712	chr7:64329292-64329293	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs6964401	chr7:64329310-64329311	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs151329980	chr7:64329320-64329321	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs376447018	chr7:64329408-64329409	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs567124947	chr7:64329457-64329458	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs189550452	chr7:64329471-64329472	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs370670370	chr7:64329494-64329495	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs4382350	chr7:64329498-64329499	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs147054989	chr7:64329552-64329553	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs534248056	chr7:64329564-64329565	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs555573800	chr7:64329660-64329661	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs191435830	chr7:64329695-64329696	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs577151958	chr7:64329700-64329701	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs113661077	chr7:64329730-64329731	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs539881069	chr7:64329756-64329757	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs4502993	chr7:64329775-64329776	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs28434608	chr7:64329819-64329820	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs112013237	chr7:64329825-64329826	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs3033156	chr7:64329826-64329827	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs201553613	chr7:64329832-64329833	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs71061320	chr7:64329834-64329835	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:80)

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
Williams Syndrome	20824207	CNVD
Cognitive impairment	21505072	CNVD
Schizophrenia	20967226	CNVD
Cancer	21272361	CNVD

Chromatin state (count:403 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:64322800-64331600	Weak transcription	Right Atrium	heart
2	chr7:64332600-64333200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr7:64333200-64335000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr7:64334000-64335800	Enhancers	Breast Myoepithelial Primary Cells	Breast
5	chr7:64334200-64334400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr7:64334200-64335200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr7:64334400-64334800	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr7:64334400-64335200	Enhancers	Osteobl	bone
9	chr7:64334600-64335000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr7:64334600-64335000	Enhancers	Dnd41	blood
11	chr7:64334800-64335200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr7:64335000-64335600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr7:64335200-64337000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chr7:64335800-64337400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
15	chr7:64336600-64337000	Active TSS	Brain Cingulate Gyrus	brain
16	chr7:64337000-64337200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
17	chr7:64337000-64337400	Enhancers	Brain Cingulate Gyrus	brain
18	chr7:64337200-64337400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr7:64337200-64337400	Enhancers	Cortex derived primary cultured neurospheres	brain
20	chr7:64337200-64337400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
21	chr7:64337200-64337400	Enhancers	Brain Anterior Caudate	brain
22	chr7:64337200-64337400	Active TSS	Brain Substantia Nigra	brain
23	chr7:64337200-64337400	Enhancers	Colon Smooth Muscle	Colon
24	chr7:64337200-64337400	Enhancers	Fetal Brain Female	brain
25	chr7:64337200-64337400	Bivalent/Poised TSS	Stomach Smooth Muscle	stomach
26	chr7:64337200-64337600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
27	chr7:64337200-64338000	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
28	chr7:64337200-64338600	Active TSS	Brain Inferior Temporal Lobe	brain
29	chr7:64337400-64337600	Enhancers	Breast Myoepithelial Primary Cells	Breast
30	chr7:64337400-64337600	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
31	chr7:64337400-64337600	Enhancers	Primary hematopoietic stem cells short term culture	blood
32	chr7:64337400-64337600	Enhancers	Primary T helper cells PMA-I stimulated	--
33	chr7:64337400-64337600	Enhancers	Primary T helper cells fromperipheralblood	blood
34	chr7:64337400-64337600	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
35	chr7:64337400-64337600	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr7:64337400-64337600	Enhancers	Adipose Nuclei	Adipose
37	chr7:64337400-64337600	Enhancers	Fetal Brain Male	brain
38	chr7:64337400-64337600	Enhancers	Fetal Heart	heart
39	chr7:64337400-64337600	Enhancers	Fetal Muscle Leg	muscle
40	chr7:64337400-64337600	Enhancers	Pancreas	Pancrea
41	chr7:64337400-64337600	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
42	chr7:64337400-64337600	Active TSS	Stomach Smooth Muscle	stomach
43	chr7:64337400-64337800	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr7:64337400-64337800	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
45	chr7:64337400-64337800	Bivalent Enhancer	Primary B cells from peripheral blood	blood
46	chr7:64337400-64337800	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
47	chr7:64337400-64337800	Flanking Active TSS	Brain Anterior Caudate	brain
48	chr7:64337400-64337800	Flanking Active TSS	Brain Hippocampus Middle	brain
49	chr7:64337400-64337800	Flanking Active TSS	Brain Substantia Nigra	brain
50	chr7:64337400-64337800	Flanking Active TSS	Colon Smooth Muscle	Colon

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