Variant report

Variant	nsv888535
Chromosome Location	chr7:80277632-80303350
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	ARID3A	chr7:80288875-80289153	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:80284287-80284555	HepG2	liver:	n/a	n/a
3	BRCA1	chr7:80288768-80289107	Hela-S3	cervix:	n/a	n/a
4	BRCA1	chr7:80302176-80302364	Hela-S3	cervix:	n/a	n/a
5	CHD1	chr7:80287800-80289162	IMR90	lung:	n/a	n/a
6	CTCF	chr7:80291140-80291290	HL-60	blood:	n/a	chr7:80291229-80291247
7	CTCF	chr7:80291171-80291320	A549	lung:	n/a	chr7:80291229-80291247
8	CTCF	chr7:80291183-80291288	GM19238	blood:	n/a	chr7:80291229-80291247
9	CTCF	chr7:80291154-80291327	MCF-7	breast:	n/a	chr7:80291229-80291247
10	CTCF	chr7:80291160-80291310	MCF-7	breast:	n/a	chr7:80291229-80291247
11	CTCF	chr7:80288874-80289086	GM10266	blood:	n/a	chr7:80288970-80288988 chr7:80288971-80288987 chr7:80288965-80288986
12	CTCF	chr7:80291200-80291350	HPF	lung:	n/a	chr7:80291229-80291247
13	CTCF	chr7:80288860-80289010	GM12878	blood:	n/a	chr7:80288970-80288988 chr7:80288971-80288987 chr7:80288965-80288986
14	CTCF	chr7:80291160-80291310	GM12866	blood:	n/a	chr7:80291229-80291247
15	CTCF	chr7:80288880-80289030	SK-N-SH_RA	brain:	n/a	chr7:80288970-80288988 chr7:80288971-80288987 chr7:80288965-80288986
16	CTCF	chr7:80288926-80289079	GM20000	blood:	n/a	chr7:80288970-80288988 chr7:80288971-80288987 chr7:80288965-80288986
17	CTCF	chr7:80288940-80289090	SAEC	small airway:	n/a	chr7:80288970-80288988 chr7:80288971-80288987 chr7:80288965-80288986
18	CTCF	chr7:80291750-80291817	MCF-7	breast:	n/a	n/a
19	CTCF	chr7:80291140-80291290	HA-sp	spinal cord:	n/a	chr7:80291229-80291247
20	CTCF	chr7:80291117-80291356	Gliobla	brain:	n/a	chr7:80291229-80291247
21	CTCF	chr7:80288693-80289167	GM12878	blood:	n/a	chr7:80288970-80288988 chr7:80288971-80288987 chr7:80288965-80288986
22	CTCF	chr7:80288900-80289050	Hela-S3	cervix:	n/a	chr7:80288970-80288988 chr7:80288971-80288987 chr7:80288965-80288986
23	CTCF	chr7:80288860-80289010	GM12871	blood:	n/a	chr7:80288970-80288988 chr7:80288971-80288987 chr7:80288965-80288986
24	CTCF	chr7:80291160-80291310	HPAF	blood vessel:	n/a	chr7:80291229-80291247
25	CTCF	chr7:80289020-80289170	MCF-7	breast:	n/a	n/a
26	CTCF	chr7:80288820-80288970	HVMF	connective:	n/a	n/a
27	CTCF	chr7:80288560-80288710	GM12873	blood:	n/a	n/a
28	CTCF	chr7:80291200-80291350	GM12878	blood:	n/a	chr7:80291229-80291247
29	CTCF	chr7:80291193-80291269	Medullo	brain:	n/a	chr7:80291229-80291247
30	CTCF	chr7:80288832-80289063	HepG2	liver:	n/a	chr7:80288970-80288988 chr7:80288971-80288987 chr7:80288965-80288986
31	CTCF	chr7:80288920-80289070	GM12801	blood:	n/a	chr7:80288970-80288988 chr7:80288971-80288987 chr7:80288965-80288986
32	CTCF	chr7:80291121-80291403	GM12878	blood:	n/a	chr7:80291229-80291247
33	CTCF	chr7:80288860-80289010	GM12869	blood:	n/a	chr7:80288970-80288988 chr7:80288971-80288987 chr7:80288965-80288986
34	CTCF	chr7:80288920-80289070	AG04450	lung:	n/a	chr7:80288970-80288988 chr7:80288971-80288987 chr7:80288965-80288986
35	CTCF	chr7:80288900-80289050	AG10803	skin:	n/a	chr7:80288970-80288988 chr7:80288971-80288987 chr7:80288965-80288986
36	CTCF	chr7:80291220-80291370	HBMEC	blood vessel:	n/a	chr7:80291229-80291247
37	CTCF	chr7:80291180-80291330	HUVEC	blood vessel:	n/a	chr7:80291229-80291247
38	CTCF	chr7:80291120-80291270	WI-38	lung:	n/a	chr7:80291229-80291247
39	CTCF	chr7:80291140-80291290	HUVEC	blood vessel:	n/a	chr7:80291229-80291247
40	CTCF	chr7:80288864-80289130	HUVEC	blood vessel:	n/a	chr7:80288970-80288988 chr7:80288971-80288987 chr7:80288965-80288986
41	CTCF	chr7:80288874-80289091	GM12878	blood:	n/a	chr7:80288970-80288988 chr7:80288971-80288987 chr7:80288965-80288986
42	CTCF	chr7:80288900-80289050	HPF	lung:	n/a	chr7:80288970-80288988 chr7:80288971-80288987 chr7:80288965-80288986
43	CTCF	chr7:80291160-80291310	HPF	lung:	n/a	chr7:80291229-80291247
44	CTCF	chr7:80291140-80291290	AG09309	skin:	n/a	chr7:80291229-80291247
45	CTCF	chr7:80288851-80289104	Lung_OC	lung:	n/a	chr7:80288970-80288988 chr7:80288971-80288987 chr7:80288965-80288986
46	CTCF	chr7:80291140-80291290	GM12870	blood:	n/a	chr7:80291229-80291247
47	CTCF	chr7:80288880-80289030	GM12873	blood:	n/a	chr7:80288970-80288988 chr7:80288971-80288987 chr7:80288965-80288986
48	CTCF	chr7:80288800-80288950	NHEK	skin:	n/a	n/a
49	CTCF	chr7:80291089-80291376	H1-hESC	embryonic stem cell:	n/a	chr7:80291229-80291247
50	CTCF	chr7:80291160-80291310	HMEC	breast:	n/a	chr7:80291229-80291247

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:80291794-80291844	HUVEC	blood vessel:	n/a
2	chr7:80291832-80291882	GM06990	blood:	n/a
3	chr7:80291794-80291844	ECC-1	luminal epithelium:	n/a
4	chr7:80291794-80291844	NB4	blood:	n/a
5	chr7:80291794-80291844	AG09319	gingival:	n/a
6	chr7:80291794-80291844	HCT-116	colon:	n/a
7	chr7:80291832-80291882	HEEpiC	esophagus:	n/a
8	chr7:80291794-80291844	HAEpiC	amniotic membrane:	n/a
9	chr7:80291794-80291844	HNPCEpiC	eye:	n/a
10	chr7:80291832-80291882	HL-60	blood:	n/a
11	chr7:80291832-80291882	Hepatocyte	liver:	n/a
12	chr7:80291832-80291882	HRPEpiC	eye:	n/a
13	chr7:80291794-80291844	ovcar-3	ovarian:	n/a
14	chr7:80291832-80291882	HPAEpiC	pulmonary alveolar:	n/a
15	chr7:80291832-80291882	NHBE	bronchial:	n/a
16	chr7:80291794-80291844	BJ	skin:	n/a
17	chr7:80291832-80291882	T-47D	breast:	n/a
18	chr7:80291832-80291882	ECC-1	luminal epithelium:	n/a
19	chr7:80291832-80291882	PFSK-1	brain:	n/a
20	chr7:80291832-80291882	NHDF-neo	bronchial:	n/a
21	chr7:80291794-80291844	PFSK-1	brain:	n/a
22	chr7:80291794-80291844	CMK	blood:	n/a
23	chr7:80291832-80291882	HAEpiC	amniotic membrane:	n/a
24	chr7:80291794-80291844	GM19239	blood:	n/a
25	chr7:80291832-80291882	GM12878	blood:	n/a
26	chr7:80291832-80291882	SK-N-SH	brain:	n/a
27	chr7:80291794-80291844	AG09309	skin:	n/a
28	chr7:80291832-80291882	ovcar-3	ovarian:	n/a
29	chr7:80291794-80291844	SAEC	small airway:	n/a
30	chr7:80291794-80291844	SK-N-SH	brain:	n/a
31	chr7:80291832-80291882	NT2-D1	testis:	n/a
32	chr7:80291832-80291882	HCF	heart:	n/a
33	chr7:80291794-80291844	HPAEpiC	pulmonary alveolar:	n/a
34	chr7:80291832-80291882	AG04449	skin:	fetal
35	chr7:80291794-80291844	SKMC	muscle:	n/a
36	chr7:80291794-80291844	SK-N-MC	brain:	n/a
37	chr7:80291832-80291882	GM12891	blood:	n/a
38	chr7:80291794-80291844	MCF10A-Er-Src	breast:	n/a
39	chr7:80291794-80291844	AG04450	lung:	fetal
40	chr7:80291832-80291882	HMEC	breast:	n/a
41	chr7:80291794-80291844	AG10803	skin:	n/a
42	chr7:80291832-80291882	SKMC	muscle:	n/a
43	chr7:80291832-80291882	HRCEpiC	kidney:	n/a
44	chr7:80291794-80291844	GM12892	blood:	n/a
45	chr7:80291832-80291882	AG04450	lung:	fetal
46	chr7:80291832-80291882	HNPCEpiC	eye:	n/a
47	chr7:80291794-80291844	PANC-1	pancreas:	n/a
48	chr7:80291832-80291882	RPTEC	kidney:	n/a
49	chr7:80291832-80291882	GM12892	blood:	n/a
50	chr7:80291832-80291882	GM19239	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:80290704..80291673-chr7:80310324..80310826,2	MCF-7	breast:
2	chr7:80057613..80058392-chr7:80288390..80289288,3	MCF-7	breast:
3	chr7:80288156..80289657-chr7:80291382..80293831,2	K562	blood:
4	chr7:80291053..80291665-chr7:81099051..81099939,2	MCF-7	breast:
5	chr7:80296853..80299195-chr7:80307235..80310003,2	MCF-7	breast:
6	chr7:80057471..80058066-chr7:80288234..80289022,3	MCF-7	breast:

Variant related genes	Relation type
CD36	TF binding region
ENSG00000229436	TF binding region
CD36	CpG island
ENSG00000229436	CpG island
ENSG00000229436	chromatin interactions

Extended variants
information (count: 1279 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:1279 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3211812	chr7:80277632-80277633	Strong transcription Weak transcription Genic enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs80154165	chr7:80277638-80277639	Strong transcription Weak transcription Genic enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs398085914	chr7:80277639-80277640	Strong transcription Weak transcription Genic enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs370709318	chr7:80277684-80277685	Strong transcription Weak transcription Genic enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs143391979	chr7:80277688-80277689	Strong transcription Weak transcription Genic enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs139286625	chr7:80277689-80277690	Strong transcription Weak transcription Genic enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs184241939	chr7:80277697-80277698	Strong transcription Weak transcription Genic enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs565199590	chr7:80277732-80277733	Strong transcription Weak transcription Genic enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs3211813	chr7:80277743-80277744	Strong transcription Weak transcription Genic enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs546965102	chr7:80277747-80277748	Strong transcription Weak transcription Genic enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs560331913	chr7:80277768-80277769	Strong transcription Weak transcription Genic enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs3211814	chr7:80277776-80277777	Strong transcription Weak transcription Genic enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs146962779	chr7:80277796-80277797	Strong transcription Weak transcription Genic enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs549466467	chr7:80277855-80277856	Strong transcription Weak transcription Genic enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs3211815	chr7:80277856-80277857	Strong transcription Weak transcription Genic enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs531558858	chr7:80277861-80277862	Strong transcription Weak transcription Genic enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs569077638	chr7:80277954-80277955	Strong transcription Weak transcription Genic enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs3211816	chr7:80277990-80277991	Strong transcription Weak transcription Genic enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs571244644	chr7:80277997-80277998	Strong transcription Weak transcription Genic enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs79053491	chr7:80278007-80278008	Strong transcription Weak transcription Genic enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs189337904	chr7:80278037-80278038	Strong transcription Weak transcription Genic enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs137976565	chr7:80278082-80278083	Strong transcription Weak transcription Genic enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs375665178	chr7:80278100-80278101	Strong transcription Weak transcription Genic enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs3211817	chr7:80278107-80278108	Strong transcription Weak transcription Genic enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs3211818	chr7:80278121-80278122	Strong transcription Weak transcription Genic enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs556628361	chr7:80278154-80278155	Strong transcription Weak transcription Genic enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs567152041	chr7:80278160-80278161	Strong transcription Weak transcription Genic enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs536304162	chr7:80278166-80278167	Strong transcription Weak transcription Genic enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs556000653	chr7:80278171-80278172	Strong transcription Weak transcription Genic enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs541494694	chr7:80278173-80278174	Strong transcription Weak transcription Genic enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs560257280	chr7:80278241-80278242	Strong transcription Weak transcription Genic enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs141633050	chr7:80278275-80278276	Strong transcription Weak transcription Genic enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs545200412	chr7:80278305-80278306	Strong transcription Weak transcription Genic enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs3211819	chr7:80278359-80278360	Strong transcription Weak transcription Genic enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs558828686	chr7:80278391-80278392	Strong transcription Weak transcription Genic enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs150496822	chr7:80278426-80278427	Strong transcription Weak transcription Genic enhancers Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs540970702	chr7:80278455-80278456	Strong transcription Weak transcription Genic enhancers Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs3211820	chr7:80278465-80278466	Strong transcription Weak transcription Genic enhancers Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs139459742	chr7:80278517-80278518	Strong transcription Weak transcription Genic enhancers Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs543083424	chr7:80278518-80278519	Strong transcription Weak transcription Genic enhancers Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs149334176	chr7:80278548-80278549	Strong transcription Weak transcription Genic enhancers Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs3211821	chr7:80278563-80278564	Strong transcription Weak transcription Genic enhancers Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs551549607	chr7:80278587-80278588	Strong transcription Weak transcription Genic enhancers Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs569180940	chr7:80278608-80278609	Strong transcription Weak transcription Genic enhancers Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs3211822	chr7:80278626-80278627	Strong transcription Weak transcription Genic enhancers Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs372223544	chr7:80278634-80278635	Strong transcription Weak transcription Genic enhancers Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs556245451	chr7:80278645-80278646	Strong transcription Weak transcription Genic enhancers Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs527937053	chr7:80278646-80278647	Strong transcription Weak transcription Genic enhancers Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs547784561	chr7:80278666-80278667	Strong transcription Weak transcription Genic enhancers Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs575727301	chr7:80278680-80278681	Strong transcription Weak transcription Genic enhancers Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:84)

Disease	PMID	Source
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
Medulloblastoma	21979893	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
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Biliary cancer	19435499	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
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	16864856	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
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
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Multiple myeloma	17550852	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Neurodevelopmental disorder	22521361	CNVD
Williams Syndrome	20824207	CNVD
Metanephric adenoma	20802469	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	21364760	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Williams-beuren syndrome	16826523	CNVD
Olfactory neuroblastoma	18408657	CNVD
Wilms tumour	19318497	CNVD
Multiple myeloma	16616336	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Schizophrenia	17879154	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	16461572	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Autism	20858243	CNVD
Breast cancer	21611746	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:174 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:80269400-80305000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
2	chr7:80272000-80280400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr7:80272600-80293600	Weak transcription	Placenta	Placenta
4	chr7:80272800-80282600	Weak transcription	Fetal Heart	heart
5	chr7:80273600-80278400	Weak transcription	Small Intestine	intestine
6	chr7:80273800-80278200	Weak transcription	Skeletal Muscle Male	skeletal muscle
7	chr7:80275600-80278400	Active TSS	Duodenum Mucosa	Duodenum
8	chr7:80275800-80284200	Weak transcription	Skeletal Muscle Female	skeletal muscle
9	chr7:80275800-80288400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr7:80276000-80280800	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr7:80276200-80284200	Weak transcription	Psoas Muscle	Psoas
12	chr7:80276200-80285600	Strong transcription	Primary monocytes fromperipheralblood	blood
13	chr7:80276200-80286400	Strong transcription	Monocytes-CD14+_RO01746	blood
14	chr7:80277000-80284200	Weak transcription	Right Ventricle	heart
15	chr7:80277200-80284200	Weak transcription	Left Ventricle	heart
16	chr7:80277600-80278400	Weak transcription	Fetal Intestine Small	intestine
17	chr7:80277600-80278400	Weak transcription	Right Atrium	heart
18	chr7:80277600-80282400	Genic enhancers	Adipose Nuclei	Adipose
19	chr7:80277600-80284400	Weak transcription	Pancreatic Islets	Pancreatic Islet
20	chr7:80278200-80278600	Strong transcription	Skeletal Muscle Male	skeletal muscle
21	chr7:80278400-80278600	Enhancers	Small Intestine	intestine
22	chr7:80278400-80279000	Enhancers	Fetal Intestine Small	intestine
23	chr7:80278400-80279400	Weak transcription	Duodenum Mucosa	Duodenum
24	chr7:80278400-80280200	Active TSS	Right Atrium	heart
25	chr7:80278600-80288200	Weak transcription	Skeletal Muscle Male	skeletal muscle
26	chr7:80279000-80306600	Weak transcription	Fetal Intestine Small	intestine
27	chr7:80279400-80279800	Active TSS	Duodenum Mucosa	Duodenum
28	chr7:80279800-80303400	Weak transcription	Duodenum Mucosa	Duodenum
29	chr7:80280200-80284200	Weak transcription	Right Atrium	heart
30	chr7:80280400-80281200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr7:80280800-80281600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr7:80281200-80287200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr7:80281600-80282000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr7:80282000-80283200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr7:80282200-80291800	Weak transcription	Fetal Muscle Leg	muscle
36	chr7:80282400-80283200	Transcr. at gene 5' and 3'	Adipose Nuclei	Adipose
37	chr7:80282600-80282800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
38	chr7:80282600-80283000	Enhancers	Fetal Heart	heart
39	chr7:80282800-80284000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
40	chr7:80282800-80291000	Weak transcription	Fetal Muscle Trunk	muscle
41	chr7:80283000-80284200	Weak transcription	Fetal Heart	heart
42	chr7:80283200-80283400	Genic enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr7:80283200-80292600	Genic enhancers	Adipose Nuclei	Adipose
44	chr7:80283400-80284000	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
45	chr7:80284000-80285000	Genic enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr7:80284000-80285000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
47	chr7:80284000-80286000	Enhancers	HepG2	liver
48	chr7:80284200-80284400	Genic enhancers	Fetal Heart	heart
49	chr7:80284200-80284400	Enhancers	Pancreas	Pancrea
50	chr7:80284200-80284400	Genic enhancers	Psoas Muscle	Psoas

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