Variant report

Variant	nsv5756
Chromosome Location	chr7:56203664-56246844
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:69)
CpG islands
(count:610)
Chromatin interactive
region (count:3)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:69 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BCL3	chr7:56236009-56236239	GM12878	blood:	n/a	n/a
2	CBX3	chr7:56220474-56220770	K562	blood:	n/a	n/a
3	CEBPB	chr7:56211378-56211507	HepG2	liver:	n/a	n/a
4	CHD1	chr7:56227253-56227368	GM12878	blood:	n/a	n/a
5	CHD1	chr7:56244538-56244617	H1-hESC	embryonic stem cell:	n/a	n/a
6	CHD2	chr7:56246706-56246869	GM12878	blood:	n/a	n/a
7	CTCF	chr7:56230140-56230290	NB4	blood:	n/a	n/a
8	CTCF	chr7:56211220-56211370	NHEK	skin:	n/a	n/a
9	CTCF	chr7:56243620-56243770	SK-N-SH_RA	brain:	n/a	n/a
10	CTCF	chr7:56230180-56230330	SK-N-SH_RA	brain:	n/a	n/a
11	CTCF	chr7:56230220-56230370	WERI-Rb-1	eye:	n/a	n/a
12	CTCF	chr7:56230120-56230270	HEK293	kidney:	n/a	n/a
13	CTCF	chr7:56228020-56228170	GM12873	blood:	n/a	n/a
14	CTCF	chr7:56207366-56207463	GM13976	blood:	n/a	n/a
15	CTCF	chr7:56243560-56243710	HRE	kidney:	n/a	n/a
16	CTCF	chr7:56243600-56243750	HRE	kidney:	n/a	n/a
17	CTCF	chr7:56236640-56236790	Caco-2	colon:	n/a	n/a
18	CTCF	chr7:56243580-56243730	HCPEpiC	choroid plexus:	n/a	n/a
19	CTCF	chr7:56232989-56233034	GM10266	blood:	n/a	n/a
20	CTCF	chr7:56243620-56243770	HepG2	liver:	n/a	n/a
21	CTCF	chr7:56206591-56206722	K562	blood:	n/a	n/a
22	CTCF	chr7:56243540-56243690	SK-N-SH_RA	brain:	n/a	n/a
23	CTCF	chr7:56230180-56230330	MCF-7	breast:	n/a	n/a
24	CUX1	chr7:56232593-56232608	GM12878	blood:	n/a	n/a
25	EGR1	chr7:56242712-56242884	K562	blood:	n/a	chr7:56242766-56242775 chr7:56242875-56242884
26	ELF1	chr7:56242371-56242625	K562	blood:	n/a	n/a
27	EP300	chr7:56211472-56211837	SK-N-SH_RA	brain:	n/a	n/a
28	FOXA1	chr7:56224880-56225238	HepG2	liver:	n/a	chr7:56225095-56225110 chr7:56225075-56225090
29	FOXA1	chr7:56224925-56225218	HepG2	liver:	n/a	chr7:56225095-56225110 chr7:56225075-56225090
30	FOXA1	chr7:56224856-56225224	HepG2	liver:	n/a	chr7:56225095-56225110 chr7:56225075-56225090
31	FOXA1	chr7:56224882-56225339	T-47D	breast:	n/a	chr7:56225095-56225110 chr7:56225075-56225090
32	FOXA1	chr7:56224882-56225255	T-47D	breast:	n/a	chr7:56225095-56225110 chr7:56225075-56225090
33	FOXA1	chr7:56224882-56225223	HepG2	liver:	n/a	chr7:56225095-56225110 chr7:56225075-56225090
34	FOXA2	chr7:56224915-56225211	HepG2	liver:	n/a	n/a
35	FOXA2	chr7:56219864-56220235	A549	lung:	n/a	n/a
36	GATA2	chr7:56211322-56212109	SH-SY5Y	brain:	n/a	n/a
37	GATA3	chr7:56243375-56243802	T-47D	breast:	n/a	n/a
38	GATA3	chr7:56211645-56212097	SH-SY5Y	brain:	n/a	n/a
39	GATA3	chr7:56203857-56204172	T-47D	breast:	n/a	n/a
40	HEY1	chr7:56230998-56231237	HepG2	liver:	n/a	n/a
41	HMGN3	chr7:56242531-56242740	K562	blood:	n/a	n/a
42	IRF1	chr7:56246762-56246767	K562	blood:	n/a	n/a
43	JUND	chr7:56211347-56211602	HepG2	liver:	n/a	n/a
44	KAP1	chr7:56220388-56220774	K562	blood:	n/a	n/a
45	KAP1	chr7:56224598-56225439	HEK293	kidney:	n/a	chr7:56224720-56224728
46	KAP1	chr7:56236122-56237262	U2OS	brain:	n/a	chr7:56237019-56237027
47	KAP1	chr7:56236224-56236910	HEK293	kidney:	n/a	n/a
48	KAP1	chr7:56212644-56213149	HEK293	kidney:	n/a	n/a
49	KAP1	chr7:56224671-56225541	U2OS	brain:	n/a	chr7:56224720-56224728
50	MAX	chr7:56242770-56243228	ECC-1	luminal epithelium:	n/a	n/a

(count:610 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:56242181-56242231	ovcar-3	ovarian:	n/a
2	chr7:56246843-56246893	BJ	skin:	n/a
3	chr7:56241697-56241747	NHBE	bronchial:	n/a
4	chr7:56243524-56243574	CMK	blood:	n/a
5	chr7:56246843-56246893	HepG2	liver:	n/a
6	chr7:56242407-56242457	SAEC	small airway:	n/a
7	chr7:56242142-56242192	HRE	kidney:	n/a
8	chr7:56242142-56242192	ProgFib	skin:	n/a
9	chr7:56243297-56243347	NHBE	bronchial:	n/a
10	chr7:56241697-56241747	K562	blood:	n/a
11	chr7:56242554-56242604	T-47D	breast:	n/a
12	chr7:56241697-56241747	NHDF-neo	bronchial:	n/a
13	chr7:56242072-56242122	HepG2	liver:	n/a
14	chr7:56242554-56242604	AG09309	skin:	n/a
15	chr7:56241697-56241747	SK-N-SH	brain:	n/a
16	chr7:56243524-56243574	Hepatocyte	liver:	n/a
17	chr7:56242142-56242192	AG04450	lung:	fetal
18	chr7:56242072-56242122	Hela-S3	cervix:	n/a
19	chr7:56246843-56246893	A549	lung:	n/a
20	chr7:56242407-56242457	Caco-2	colon:	n/a
21	chr7:56242072-56242122	Jurkat	blood:	n/a
22	chr7:56241697-56241747	H1-hESC	embryonic stem cell:	embryo
23	chr7:56242407-56242457	IMR90	lung:	fetal
24	chr7:56243524-56243574	IMR90	lung:	fetal
25	chr7:56242142-56242192	BE2_C	brain:	n/a
26	chr7:56242554-56242604	ovcar-3	ovarian:	n/a
27	chr7:56242554-56242604	ProgFib	skin:	n/a
28	chr7:56243524-56243574	SK-N-SH_RA	brain:	n/a
29	chr7:56242801-56242851	HCF	heart:	n/a
30	chr7:56241697-56241747	NH-A	brain:	n/a
31	chr7:56242554-56242604	HCF	heart:	n/a
32	chr7:56242407-56242457	NH-A	brain:	n/a
33	chr7:56242554-56242604	MCF-7	breast:	n/a
34	chr7:56242801-56242851	SK-N-MC	brain:	n/a
35	chr7:56242142-56242192	PrEC	prostate:	n/a
36	chr7:56242407-56242457	K562	blood:	n/a
37	chr7:56242801-56242851	HEEpiC	esophagus:	n/a
38	chr7:56242072-56242122	ProgFib	skin:	n/a
39	chr7:56242801-56242851	HIPEpiC	eye:	n/a
40	chr7:56242801-56242851	PrEC	prostate:	n/a
41	chr7:56242554-56242604	Caco-2	colon:	n/a
42	chr7:56242072-56242122	NH-A	brain:	n/a
43	chr7:56241697-56241747	PrEC	prostate:	n/a
44	chr7:56243297-56243347	Caco-2	colon:	n/a
45	chr7:56242801-56242851	AG09309	skin:	n/a
46	chr7:56242181-56242231	HEEpiC	esophagus:	n/a
47	chr7:56243297-56243347	SK-N-SH_RA	brain:	n/a
48	chr7:56242181-56242231	NHDF-neo	bronchial:	n/a
49	chr7:56246843-56246893	HL-60	blood:	n/a
50	chr7:56242181-56242231	BJ	skin:	n/a

(count:3 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:56234975..56237932-chr7:56245748..56248480,2	MCF-7	breast:
2	chr7:56199736..56202207-chr7:56205046..56206686,2	K562	blood:
3	chr7:56234975..56237932-chr7:56245748..56248480,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SUMF2-9	chr7:56243327-56244105	NONHSAT120737

No data

Variant related genes	Relation type
ENSG00000230191	TF binding region
ENSG00000233028	TF binding region
ENSG00000230191	CpG island
ENSG00000233028	CpG island

Extended variants
information (count: 815 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:815 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs538090073	chr7:56206401-56206402	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs544671711	chr7:56206412-56206413	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs150225931	chr7:56206464-56206465	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs375053563	chr7:56206486-56206487	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs138829613	chr7:56206514-56206515	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs190740809	chr7:56206543-56206544	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs149368764	chr7:56206550-56206551	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs373161765	chr7:56206565-56206566	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs71543792	chr7:56206571-56206572	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs572077009	chr7:56206598-56206599	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs533945306	chr7:56222084-56222085	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs193231384	chr7:56222121-56222122	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs551450022	chr7:56222144-56222145	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs547868275	chr7:56222178-56222179	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs182697124	chr7:56222181-56222182	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs530506307	chr7:56222185-56222186	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs190533476	chr7:56223005-56223006	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs572895747	chr7:56223076-56223077	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs534648979	chr7:56223081-56223082	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs117409866	chr7:56223099-56223100	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs118185979	chr7:56223110-56223111	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs142335789	chr7:56223127-56223128	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs698646	chr7:56223152-56223153	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs150279812	chr7:56223187-56223188	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs577561971	chr7:56223256-56223257	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs79371219	chr7:56223268-56223269	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs34574482	chr7:56223271-56223272	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs698647	chr7:56223305-56223306	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs560911940	chr7:56223333-56223334	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs56309554	chr7:56223362-56223363	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs75939732	chr7:56223368-56223369	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs55850146	chr7:56223369-56223370	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs397805636	chr7:56223385-56223386	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs192089929	chr7:56224802-56224803	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs541992182	chr7:56224834-56224835	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs78225581	chr7:56224863-56224864	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs184027441	chr7:56224870-56224871	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs150772293	chr7:56224914-56224915	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs552386013	chr7:56224919-56224920	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs533760404	chr7:56224933-56224934	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs570852805	chr7:56224938-56224939	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs139659597	chr7:56224958-56224959	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs117442885	chr7:56225010-56225011	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs569143437	chr7:56225055-56225056	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs187599578	chr7:56225071-56225072	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs189549003	chr7:56225092-56225093	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs1851894	chr7:56225195-56225196	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs566660379	chr7:56225207-56225208	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs182616032	chr7:56225277-56225278	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs187136309	chr7:56225283-56225284	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:83)

Disease	PMID	Source
Neuroblastoma	18923191	CNVD
Wilms tumour	21544195	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Medulloblastoma	21979893	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
colon cancer	17210682	CNVD
Lung adenocarcinoma	21810691	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Colorectal cancer	19359472	CNVD
Hypothalamic hamartomas	18252217	CNVD
Human rectal carcinomas	16397240	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Medulloblastoma	18056178	CNVD
Basal cell lymphoma	17170743	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	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
Endometrioid adenocarcinoma	16974079	CNVD
Autism	22495311	CNVD
Biliary cancer	19435499	CNVD
Cancer	21183584	CNVD
Follicular lymphoma	20505157	CNVD
Williams-beuren syndrome	22470819	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21750150	CNVD
Hepatocellular carcinoma	16750200	CNVD
Non-small cell lung cancer	21829676	CNVD
Gastric cancer	24379144	CNVD
Glioblastoma multiforme	17002787	CNVD
Lung cancer	18438408	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	21364760	CNVD
Esophageal cancer	21851588	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	16864856	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Glioblastoma multiforme	22291905	CNVD
Glioblastoma multiforme	19435819	CNVD
Intracranial ependymoma	16609018	CNVD
Lung cancer	21911935	CNVD
Urothelial cell carcinoma	18451213	CNVD
Breast cancer	21990379	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Colorectal cancer	19455253	CNVD
Lung cancer	17925434	CNVD
Glioma	24330732	CNVD
Lung adenocarcinoma	23938291	CNVD
Glioma	17634744	CNVD
Oral squamous cell carcinoma	19276369	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Lung cancer	20031968	CNVD
Glioblastoma	17090523	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Glioma	17123091	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Medullary thyroid carcinoma	18765511	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:56206400-56206600	Enhancers	Left Ventricle	heart
2	chr7:56222000-56222200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr7:56223000-56223400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr7:56224800-56225600	Enhancers	HepG2	liver
5	chr7:56227400-56227800	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
6	chr7:56228200-56228600	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
7	chr7:56229200-56231800	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
8	chr7:56234200-56237600	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
9	chr7:56235600-56236600	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
10	chr7:56235800-56236200	Active TSS	Fetal Lung	lung
11	chr7:56236200-56239800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
12	chr7:56238200-56239200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
13	chr7:56238400-56238600	Enhancers	Adipose Nuclei	Adipose
14	chr7:56239200-56242000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
15	chr7:56241000-56242200	Weak transcription	Adipose Nuclei	Adipose
16	chr7:56242000-56242600	ZNF genes & repeats	Fetal Adrenal Gland	Adrenal Gland
17	chr7:56242000-56243800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr7:56242200-56242400	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
19	chr7:56242200-56242400	Enhancers	Adipose Nuclei	Adipose
20	chr7:56242200-56243000	Enhancers	Pancreas	Pancrea
21	chr7:56242200-56243400	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
22	chr7:56242200-56243400	ZNF genes & repeats	Lung	lung
23	chr7:56242200-56243600	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr7:56242200-56244000	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr7:56242400-56242600	Active TSS	Breast Myoepithelial Primary Cells	Breast
26	chr7:56242400-56242600	Enhancers	Ovary	ovary
27	chr7:56242400-56242800	Flanking Active TSS	Adipose Nuclei	Adipose
28	chr7:56242400-56242800	Flanking Active TSS	Right Ventricle	heart
29	chr7:56242400-56243000	Bivalent/Poised TSS	Brain Inferior Temporal Lobe	brain
30	chr7:56242400-56243000	Active TSS	Right Atrium	heart
31	chr7:56242400-56243000	Bivalent/Poised TSS	Skeletal Muscle Male	skeletal muscle
32	chr7:56242400-56243200	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
33	chr7:56242400-56243400	ZNF genes & repeats	Brain Germinal Matrix	brain
34	chr7:56242400-56243400	Active TSS	Gastric	stomach
35	chr7:56242400-56243600	Bivalent/Poised TSS	Duodenum Smooth Muscle	Duodenum
36	chr7:56242400-56243600	Active TSS	Rectal Smooth Muscle	rectum
37	chr7:56242400-56243800	Active TSS	Aorta	Aorta
38	chr7:56242400-56243800	Bivalent/Poised TSS	Brain Hippocampus Middle	brain
39	chr7:56242400-56243800	ZNF genes & repeats	Spleen	Spleen
40	chr7:56242400-56244000	Active TSS	Colon Smooth Muscle	Colon
41	chr7:56242400-56244000	Bivalent/Poised TSS	Stomach Smooth Muscle	stomach
42	chr7:56242600-56242800	Flanking Bivalent TSS/Enh	Breast Myoepithelial Primary Cells	Breast
43	chr7:56242600-56242800	Flanking Bivalent TSS/Enh	Cortex derived primary cultured neurospheres	brain
44	chr7:56242600-56242800	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin02	Skin
45	chr7:56242600-56242800	Flanking Bivalent TSS/Enh	Fetal Adrenal Gland	Adrenal Gland
46	chr7:56242600-56242800	Flanking Bivalent TSS/Enh	Fetal Muscle Trunk	muscle
47	chr7:56242600-56242800	Flanking Bivalent TSS/Enh	Placenta	Placenta
48	chr7:56242600-56242800	Flanking Active TSS	Ovary	ovary
49	chr7:56242600-56242800	Flanking Bivalent TSS/Enh	Psoas Muscle	Psoas
50	chr7:56242600-56243000	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell

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