Variant report

Variant	nsv607680
Chromosome Location	chr7:80097576-80142217
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:421)
CpG islands
(count:61)
Chromatin interactive
region (count:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:421 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:80128367-80129128	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:80117772-80117988	HepG2	liver:	n/a	n/a
3	BACH1	chr7:80104300-80104503	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr7:80110643-80110676	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr7:80107995-80108383	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr7:80128743-80128980	H1-hESC	embryonic stem cell:	n/a	n/a
7	BCL3	chr7:80127785-80128117	GM12878	blood:	n/a	n/a
8	BCL3	chr7:80112328-80112532	GM12878	blood:	n/a	n/a
9	BRCA1	chr7:80110448-80110844	Hela-S3	cervix:	n/a	n/a
10	CBX3	chr7:80108002-80108365	HCT-116	colon:	n/a	n/a
11	CCNT2	chr7:80097910-80098110	K562	blood:	n/a	n/a
12	CCNT2	chr7:80127711-80127911	K562	blood:	n/a	n/a
13	CEBPB	chr7:80115162-80115578	IMR90	lung:	n/a	n/a
14	CEBPB	chr7:80128218-80128933	IMR90	lung:	n/a	n/a
15	CEBPB	chr7:80117784-80118057	A549	lung:	n/a	chr7:80117893-80117904
16	CEBPB	chr7:80128357-80128974	MCF-7	breast:	n/a	n/a
17	CEBPB	chr7:80117713-80118087	HepG2	liver:	n/a	chr7:80117893-80117904
18	CEBPB	chr7:80117734-80118078	IMR90	lung:	n/a	chr7:80117893-80117904
19	CEBPB	chr7:80117764-80118029	H1-hESC	embryonic stem cell:	n/a	chr7:80117893-80117904
20	CEBPB	chr7:80128302-80128946	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr7:80112355-80112659	IMR90	lung:	n/a	n/a
22	CEBPB	chr7:80108091-80108406	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr7:80102216-80102549	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chr7:80110545-80110722	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPB	chr7:80112396-80112598	A549	lung:	n/a	n/a
26	CEBPB	chr7:80117713-80118094	Hela-S3	cervix:	n/a	chr7:80117893-80117904
27	CEBPB	chr7:80110488-80110956	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr7:80135250-80135976	MCF-7	breast:	n/a	chr7:80135843-80135854
29	CEBPB	chr7:80112375-80112643	HepG2	liver:	n/a	n/a
30	CEBPB	chr7:80110550-80110853	MCF-7	breast:	n/a	n/a
31	CEBPB	chr7:80112308-80112686	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chr7:80128375-80128965	A549	lung:	n/a	n/a
33	CEBPB	chr7:80127695-80128252	GM12878	blood:	n/a	n/a
34	CEBPB	chr7:80128659-80128970	HepG2	liver:	n/a	n/a
35	CEBPB	chr7:80099344-80099951	Hela-S3	cervix:	n/a	n/a
36	CEBPB	chr7:80128270-80128909	A549	lung:	n/a	n/a
37	CHD2	chr7:80099399-80099702	Hela-S3	cervix:	n/a	n/a
38	CHD2	chr7:80128466-80128949	Hela-S3	cervix:	n/a	n/a
39	CHD2	chr7:80110525-80110863	Hela-S3	cervix:	n/a	n/a
40	CTCF	chr7:80120140-80120290	GM06990	blood:	n/a	n/a
41	CTCF	chr7:80107180-80107330	RPTEC	kidney:	n/a	n/a
42	CTCF	chr7:80133369-80133438	Lung_OC	lung:	n/a	n/a
43	CTCF	chr7:80120160-80120310	MCF-7	breast:	n/a	n/a
44	CTCF	chr7:80114480-80114520	GM13976	blood:	n/a	n/a
45	E2F4	chr7:80107993-80108240	MCF10A-Er-Src	breast:	n/a	n/a
46	E2F4	chr7:80128353-80128879	MCF10A-Er-Src	breast:	n/a	n/a
47	E2F4	chr7:80138764-80138896	MCF10A-Er-Src	breast:	n/a	n/a
48	EP300	chr7:80099318-80099653	Hela-S3	cervix:	n/a	n/a
49	EP300	chr7:80128366-80129166	SK-N-SH	brain:	n/a	chr7:80128989-80129003 chr7:80128587-80128594
50	EP300	chr7:80110389-80110997	ECC-1	luminal epithelium:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:80142060-80142110	ProgFib	skin:	n/a
2	chr7:80142060-80142110	HAEpiC	amniotic membrane:	n/a
3	chr7:80142060-80142110	Jurkat	blood:	n/a
4	chr7:80142060-80142110	NHBE	bronchial:	n/a
5	chr7:80142060-80142110	T-47D	breast:	n/a
6	chr7:80142060-80142110	AoSMC	blood vessel:	n/a
7	chr7:80142060-80142110	GM12892	blood:	n/a
8	chr7:80142060-80142110	BJ	skin:	n/a
9	chr7:80142060-80142110	HNPCEpiC	eye:	n/a
10	chr7:80142060-80142110	AG04449	skin:	fetal
11	chr7:80142060-80142110	SKMC	muscle:	n/a
12	chr7:80142060-80142110	AG09309	skin:	n/a
13	chr7:80142060-80142110	NHDF-neo	bronchial:	n/a
14	chr7:80142060-80142110	HCF	heart:	n/a
15	chr7:80142060-80142110	AG10803	skin:	n/a
16	chr7:80142060-80142110	HUVEC	blood vessel:	n/a
17	chr7:80142060-80142110	CMK	blood:	n/a
18	chr7:80142060-80142110	GM12878	blood:	n/a
19	chr7:80142060-80142110	SK-N-SH	brain:	n/a
20	chr7:80142060-80142110	IMR90	lung:	fetal
21	chr7:80142060-80142110	SK-N-MC	brain:	n/a
22	chr7:80142060-80142110	PFSK-1	brain:	n/a
23	chr7:80142060-80142110	ECC-1	luminal epithelium:	n/a
24	chr7:80142060-80142110	H1-hESC	embryonic stem cell:	embryo
25	chr7:80142060-80142110	NB4	blood:	n/a
26	chr7:80142060-80142110	HCT-116	colon:	n/a
27	chr7:80142060-80142110	GM19239	blood:	n/a
28	chr7:80142060-80142110	HCPEpiC	choroid plexus:	n/a
29	chr7:80142060-80142110	HMEC	breast:	n/a
30	chr7:80142060-80142110	ovcar-3	ovarian:	n/a
31	chr7:80142060-80142110	HRPEpiC	eye:	n/a
32	chr7:80142060-80142110	MCF-7	breast:	n/a
33	chr7:80142060-80142110	BE2_C	brain:	n/a
34	chr7:80142060-80142110	HCM	heart:	n/a
35	chr7:80142060-80142110	HRE	kidney:	n/a
36	chr7:80142060-80142110	A549	lung:	n/a
37	chr7:80142060-80142110	HepG2	liver:	n/a
38	chr7:80142060-80142110	SAEC	small airway:	n/a
39	chr7:80142060-80142110	HIPEpiC	eye:	n/a
40	chr7:80142060-80142110	NH-A	brain:	n/a
41	chr7:80142060-80142110	Hepatocyte	liver:	n/a
42	chr7:80142060-80142110	GM06990	blood:	n/a
43	chr7:80142060-80142110	HEK293	kidney:	embryo
44	chr7:80142060-80142110	HRCEpiC	kidney:	n/a
45	chr7:80142060-80142110	Hela-S3	cervix:	n/a
46	chr7:80142060-80142110	K562	blood:	n/a
47	chr7:80142060-80142110	LNCaP	prostate:	n/a
48	chr7:80142060-80142110	MCF10A-Er-Src	breast:	n/a
49	chr7:80142060-80142110	SK-N-SH_RA	brain:	n/a
50	chr7:80142060-80142110	AG04450	lung:	fetal

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:80125854..80128249-chr7:80143744..80146199,2	MCF-7	breast:
2	chr7:80130973..80133838-chr7:80134281..80135849,2	MCF-7	breast:
3	chr7:80096464..80097970-chr7:80098984..80101525,2	K562	blood:
4	chr7:80102854..80105069-chr7:80112565..80115333,2	K562	blood:
5	chr7:80096594..80099585-chr7:80101660..80104577,2	MCF-7	breast:
6	chr7:80096464..80097970-chr7:80098984..80101525,2	K562	blood:
7	chr7:80130973..80133838-chr7:80134281..80135849,2	MCF-7	breast:
8	chr7:80096594..80099585-chr7:80101660..80104577,2	MCF-7	breast:
9	chr7:80102854..80105069-chr7:80112565..80115333,2	K562	blood:

No data

Variant related genes	Relation type
GNAT3	TF binding region
GNAT3	CpG island

Extended variants
information (count: 1710 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:1710 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs562384118	chr7:80097576-80097577	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs79730565	chr7:80097607-80097608	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs199663600	chr7:80097612-80097613	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs368945238	chr7:80097668-80097669	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs571104918	chr7:80097739-80097740	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs372520887	chr7:80097818-80097819	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs187313427	chr7:80097852-80097853	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs531146331	chr7:80097857-80097858	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs574239481	chr7:80097868-80097869	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs550863109	chr7:80097877-80097878	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs190937928	chr7:80097878-80097879	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs533446273	chr7:80097902-80097903	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs183135167	chr7:80097925-80097926	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs112537251	chr7:80097932-80097933	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs535433092	chr7:80097967-80097968	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs569405575	chr7:80098059-80098060	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs576553513	chr7:80098088-80098089	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs143582748	chr7:80098090-80098091	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs568228570	chr7:80098123-80098124	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs35136501	chr7:80098192-80098193	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs537272539	chr7:80098197-80098198	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs186659272	chr7:80098233-80098234	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs146889193	chr7:80098392-80098393	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs576565114	chr7:80098424-80098425	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs545511157	chr7:80098452-80098453	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs539138169	chr7:80098469-80098470	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs799930	chr7:80098487-80098488	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs116980660	chr7:80098524-80098525	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs191117282	chr7:80098567-80098568	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs12671431	chr7:80098568-80098569	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs575022173	chr7:80098585-80098586	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs575822553	chr7:80098692-80098693	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs370523735	chr7:80098716-80098717	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs544821603	chr7:80098744-80098745	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs564658385	chr7:80098804-80098805	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs533510047	chr7:80098818-80098819	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs541194895	chr7:80098823-80098824	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs17153990	chr7:80098864-80098865	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs554558721	chr7:80098880-80098881	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs560528753	chr7:80098881-80098882	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs577101967	chr7:80098901-80098902	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs529302148	chr7:80098953-80098954	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs34783603	chr7:80098968-80098969	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs549079505	chr7:80098992-80098993	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs568371780	chr7:80099067-80099068	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs574400998	chr7:80099071-80099072	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs139748035	chr7:80099084-80099085	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs570311523	chr7:80099085-80099086	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs539201927	chr7:80099143-80099144	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs552661287	chr7:80099239-80099240	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:83)

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
Cancer	20164919	CNVD
Breast cancer	21611746	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:392 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:80094600-80098400	Enhancers	Pancreatic Islets	Pancreatic Islet
2	chr7:80095600-80097800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr7:80095600-80106800	Weak transcription	Right Atrium	heart
4	chr7:80096600-80101200	Weak transcription	Skeletal Muscle Female	skeletal muscle
5	chr7:80096600-80102400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr7:80096800-80099400	Weak transcription	NH-A	brain
7	chr7:80096800-80101000	Weak transcription	Skeletal Muscle Male	skeletal muscle
8	chr7:80096800-80101600	Weak transcription	Small Intestine	intestine
9	chr7:80096800-80102000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr7:80096800-80102000	Weak transcription	Liver	Liver
11	chr7:80096800-80102000	Weak transcription	HepG2	liver
12	chr7:80096800-80113000	Enhancers	Hela-S3	cervix
13	chr7:80097000-80097800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
14	chr7:80097000-80099000	Weak transcription	Muscle Satellite Cultured Cells	--
15	chr7:80097000-80101000	Weak transcription	Adipose Nuclei	Adipose
16	chr7:80097000-80101400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr7:80097200-80100800	Weak transcription	Duodenum Mucosa	Duodenum
18	chr7:80097200-80100800	Weak transcription	Fetal Intestine Large	intestine
19	chr7:80097200-80101000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
20	chr7:80097200-80101000	Weak transcription	Fetal Heart	heart
21	chr7:80097200-80101600	Weak transcription	A549	lung
22	chr7:80097400-80100800	Weak transcription	Fetal Intestine Small	intestine
23	chr7:80097800-80098200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
24	chr7:80097800-80098600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
25	chr7:80098200-80098800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr7:80098400-80100600	Weak transcription	Pancreatic Islets	Pancreatic Islet
27	chr7:80098600-80101400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
28	chr7:80098800-80101200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr7:80099000-80099600	Enhancers	Muscle Satellite Cultured Cells	--
30	chr7:80099400-80099600	Enhancers	NH-A	brain
31	chr7:80099600-80109600	Weak transcription	NH-A	brain
32	chr7:80100600-80102200	Enhancers	Pancreatic Islets	Pancreatic Islet
33	chr7:80100800-80101000	Enhancers	Duodenum Mucosa	Duodenum
34	chr7:80100800-80102600	Enhancers	Fetal Intestine Small	intestine
35	chr7:80100800-80103600	Enhancers	Fetal Intestine Large	intestine
36	chr7:80101000-80101200	Enhancers	Adipose Nuclei	Adipose
37	chr7:80101000-80101400	Flanking Active TSS	Duodenum Mucosa	Duodenum
38	chr7:80101000-80101800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
39	chr7:80101000-80101800	Enhancers	Skeletal Muscle Male	skeletal muscle
40	chr7:80101000-80102200	Enhancers	Fetal Heart	heart
41	chr7:80101200-80101400	Flanking Active TSS	Adipose Nuclei	Adipose
42	chr7:80101200-80101400	Enhancers	Fetal Kidney	kidney
43	chr7:80101200-80101600	Weak transcription	Left Ventricle	heart
44	chr7:80101200-80101800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr7:80101200-80102600	Enhancers	Skeletal Muscle Female	skeletal muscle
46	chr7:80101400-80101600	Enhancers	Adipose Nuclei	Adipose
47	chr7:80101400-80101800	Enhancers	Duodenum Mucosa	Duodenum
48	chr7:80101400-80102400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
49	chr7:80101400-80103400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr7:80101600-80101800	Flanking Active TSS	Adipose Nuclei	Adipose

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