Variant report

Variant	nsv888063
Chromosome Location	chr7:55728476-55899496
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1116)
CpG islands
(count:1405)
Chromatin interactive
region (count:2)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1116 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:55870300-55870318	K562	blood:	n/a	n/a
2	ARID3A	chr7:55800487-55800499	K562	blood:	n/a	n/a
3	ARID3A	chr7:55766815-55767160	HepG2	liver:	n/a	n/a
4	ARID3A	chr7:55775903-55776100	K562	blood:	n/a	n/a
5	ATF1	chr7:55775814-55776082	K562	blood:	n/a	n/a
6	ATF1	chr7:55845338-55845367	K562	blood:	n/a	n/a
7	ATF1	chr7:55766863-55767175	K562	blood:	n/a	n/a
8	ATF1	chr7:55797922-55798229	K562	blood:	n/a	n/a
9	ATF3	chr7:55775794-55776151	K562	blood:	n/a	n/a
10	ATF3	chr7:55798768-55799118	K562	blood:	n/a	n/a
11	BACH1	chr7:55809638-55809751	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr7:55862322-55862529	H1-hESC	embryonic stem cell:	n/a	n/a
13	BATF	chr7:55810431-55810600	GM12878	blood:	n/a	n/a
14	BATF	chr7:55790556-55790863	GM12878	blood:	n/a	n/a
15	BATF	chr7:55809246-55809419	GM12878	blood:	n/a	n/a
16	BATF	chr7:55766911-55767148	GM12878	blood:	n/a	n/a
17	BATF	chr7:55811971-55812164	GM12878	blood:	n/a	n/a
18	BATF	chr7:55811851-55812057	GM12878	blood:	n/a	n/a
19	BATF	chr7:55820832-55821076	GM12878	blood:	n/a	chr7:55820958-55820969
20	BCL11A	chr7:55809118-55809327	GM12878	blood:	n/a	chr7:55809309-55809322
21	BCL11A	chr7:55811571-55811727	GM12878	blood:	n/a	n/a
22	BCL11A	chr7:55810305-55810522	GM12878	blood:	n/a	n/a
23	BCL11A	chr7:55809240-55809421	GM12878	blood:	n/a	chr7:55809309-55809322
24	BCL11A	chr7:55811867-55812100	GM12878	blood:	n/a	n/a
25	BCL11A	chr7:55811886-55812072	GM12878	blood:	n/a	n/a
26	BHLHE40	chr7:55811958-55812177	HepG2	liver:	n/a	n/a
27	BHLHE40	chr7:55806702-55806733	HepG2	liver:	n/a	n/a
28	BHLHE40	chr7:55766540-55767161	HepG2	liver:	n/a	n/a
29	BHLHE40	chr7:55766975-55767060	K562	blood:	n/a	n/a
30	BHLHE40	chr7:55766892-55767023	GM12878	blood:	n/a	n/a
31	CBX3	chr7:55864948-55865345	HCT-116	colon:	n/a	n/a
32	CBX3	chr7:55864935-55865274	K562	blood:	n/a	n/a
33	CBX3	chr7:55864959-55865300	K562	blood:	n/a	n/a
34	CBX3	chr7:55864939-55865388	HCT-116	colon:	n/a	n/a
35	CBX3	chr7:55893956-55894291	HCT-116	colon:	n/a	n/a
36	CEBPB	chr7:55788167-55788348	IMR90	lung:	n/a	chr7:55788232-55788243
37	CEBPB	chr7:55859780-55860090	K562	blood:	n/a	chr7:55859941-55859954 chr7:55859941-55859952
38	CEBPB	chr7:55745532-55745718	HepG2	liver:	n/a	chr7:55745647-55745658 chr7:55745649-55745658 chr7:55745648-55745659
39	CEBPB	chr7:55845510-55845585	A549	lung:	n/a	n/a
40	CEBPB	chr7:55766734-55767139	HepG2	liver:	n/a	n/a
41	CEBPB	chr7:55807053-55807253	HepG2	liver:	n/a	n/a
42	CEBPB	chr7:55862272-55862668	MCF-7	breast:	n/a	chr7:55862399-55862410
43	CEBPB	chr7:55862253-55862555	K562	blood:	n/a	chr7:55862399-55862410
44	CEBPB	chr7:55862294-55862497	HepG2	liver:	n/a	chr7:55862399-55862410
45	CEBPB	chr7:55809734-55810013	K562	blood:	n/a	n/a
46	CEBPB	chr7:55778109-55778244	A549	lung:	n/a	chr7:55778194-55778205
47	CEBPB	chr7:55855289-55855369	K562	blood:	n/a	n/a
48	CEBPB	chr7:55862241-55862744	HCT-116	colon:	n/a	chr7:55862399-55862410
49	CEBPB	chr7:55844751-55844845	H1-hESC	embryonic stem cell:	n/a	chr7:55844761-55844772
50	CEBPB	chr7:55862358-55862505	IMR90	lung:	n/a	chr7:55862399-55862410

(count:1405 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:55773068-55773118	NB4	blood:	n/a
2	chr7:55751301-55751351	IMR90	lung:	fetal
3	chr7:55773068-55773118	NB4	blood:	n/a
4	chr7:55751301-55751351	IMR90	lung:	fetal
5	chr7:55757733-55757783	K562	blood:	n/a
6	chr7:55811507-55811557	HepG2	liver:	n/a
7	chr7:55817964-55818014	RPTEC	kidney:	n/a
8	chr7:55756785-55756835	PANC-1	pancreas:	n/a
9	chr7:55840551-55840601	HCT-116	colon:	n/a
10	chr7:55812396-55812446	BJ	skin:	n/a
11	chr7:55757733-55757783	HUVEC	blood vessel:	n/a
12	chr7:55808934-55808984	MCF10A-Er-Src	breast:	n/a
13	chr7:55816154-55816204	HUVEC	blood vessel:	n/a
14	chr7:55773068-55773118	NHBE	bronchial:	n/a
15	chr7:55816154-55816204	HL-60	blood:	n/a
16	chr7:55816154-55816204	HCPEpiC	choroid plexus:	n/a
17	chr7:55811507-55811557	AG09319	gingival:	n/a
18	chr7:55810883-55810933	NHBE	bronchial:	n/a
19	chr7:55816154-55816204	HepG2	liver:	n/a
20	chr7:55807171-55807221	GM19239	blood:	n/a
21	chr7:55799739-55799789	HCPEpiC	choroid plexus:	n/a
22	chr7:55809665-55809715	HEEpiC	esophagus:	n/a
23	chr7:55757158-55757208	RPTEC	kidney:	n/a
24	chr7:55799845-55799895	AG10803	skin:	n/a
25	chr7:55811507-55811557	IMR90	lung:	fetal
26	chr7:55811507-55811557	HEEpiC	esophagus:	n/a
27	chr7:55808878-55808928	SK-N-SH	brain:	n/a
28	chr7:55811507-55811557	PANC-1	pancreas:	n/a
29	chr7:55756785-55756835	ovcar-3	ovarian:	n/a
30	chr7:55810883-55810933	HMEC	breast:	n/a
31	chr7:55757733-55757783	GM12891	blood:	n/a
32	chr7:55756785-55756835	GM19239	blood:	n/a
33	chr7:55809665-55809715	HRCEpiC	kidney:	n/a
34	chr7:55799845-55799895	AoSMC	blood vessel:	n/a
35	chr7:55756911-55756961	AG10803	skin:	n/a
36	chr7:55812396-55812446	CMK	blood:	n/a
37	chr7:55757733-55757783	HCT-116	colon:	n/a
38	chr7:55840551-55840601	K562	blood:	n/a
39	chr7:55816154-55816204	CMK	blood:	n/a
40	chr7:55812396-55812446	HUVEC	blood vessel:	n/a
41	chr7:55809665-55809715	NT2-D1	testis:	n/a
42	chr7:55757158-55757208	ProgFib	skin:	n/a
43	chr7:55758049-55758099	NHBE	bronchial:	n/a
44	chr7:55757158-55757208	SK-N-SH	brain:	n/a
45	chr7:55812396-55812446	A549	lung:	n/a
46	chr7:55808878-55808928	HNPCEpiC	eye:	n/a
47	chr7:55874624-55874674	NHBE	bronchial:	n/a
48	chr7:55757158-55757208	HCT-116	colon:	n/a
49	chr7:55816154-55816204	SK-N-MC	brain:	n/a
50	chr7:55799845-55799895	HEEpiC	esophagus:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:55782873..55785811-chr7:56031209..56033852,2	K562	blood:
2	chr7:55845241..55847686-chr7:56031025..56033785,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-15K19.2.1-3	chr7:55840872-55840935	NONHSAT120700
2	lnc-RP11-15K19.2.1-3	chr7:55832485-55832637	NONHSAT120696
3	lnc-SEPT14-2	chr7:55840870-55841028	NONHSAT120699
4	lnc-RP11-15K19.2.1-3	chr7:55840874-55840935	NONHSAT120696
5	lnc-RP11-15K19.2.1-3	chr7:55840922-55841211	NONHSAT120702
6	lnc-RP11-15K19.2.1-3	chr7:55846506-55846745	NONHSAT120700
7	lnc-PSPH-2	chr7:55865639-55866173	NONHSAT120704
8	lnc-SEPT14-2	chr7:55841348-55841546	NONHSAT120699
9	lnc-RP11-15K19.2.1-3	chr7:55846506-55846763	NONHSAT120696

No data

Variant related genes	Relation type
FKBP9L	TF binding region
SUMO2P3	TF binding region
CICP11	TF binding region
PSPHP1	TF binding region
RNU6-1126P	TF binding region
RNU6-389P	TF binding region
CICP12	TF binding region
ENSG00000229762	TF binding region
ENSG00000235738	TF binding region
ENSG00000231317	TF binding region
FKBP9L	CpG island
SUMO2P3	CpG island
CICP11	CpG island
PSPHP1	CpG island
RNU6-1126P	CpG island
RNU6-389P	CpG island
CICP12	CpG island
ENSG00000229762	CpG island
ENSG00000235738	CpG island
ENSG00000231317	CpG island
ENSG00000146729	chromatin interactions

Extended variants
information (count: 3713 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:3713 , 50 per page) page: 1 2 3 4 5 6 7 ... 75

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4440579	chr7:55729814-55729815	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs566720131	chr7:55729827-55729828	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs556100972	chr7:55729843-55729844	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs187079455	chr7:55729851-55729852	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs535547709	chr7:55729852-55729853	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs553954871	chr7:55729880-55729881	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs61587348	chr7:55729885-55729886	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs545848001	chr7:55729886-55729887	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs188300137	chr7:55729905-55729906	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs576683870	chr7:55729929-55729930	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs180704818	chr7:55729934-55729935	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs59293440	chr7:55729942-55729943	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs562149129	chr7:55730045-55730046	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs185281188	chr7:55730075-55730076	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs200884731	chr7:55730076-55730077	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs556887020	chr7:55730102-55730103	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs541120359	chr7:55730123-55730124	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs559457494	chr7:55730191-55730192	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs4320501	chr7:55730222-55730223	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs551385175	chr7:55730317-55730318	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs564373221	chr7:55730401-55730402	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs531518025	chr7:55730404-55730405	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs4388405	chr7:55730415-55730416	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs533433051	chr7:55730421-55730422	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs535686596	chr7:55730447-55730448	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs546898626	chr7:55730449-55730450	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs147572711	chr7:55730470-55730471	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs533968695	chr7:55730487-55730488	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs117486294	chr7:55730495-55730496	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs539410632	chr7:55730568-55730569	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs557482510	chr7:55730576-55730577	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs200972302	chr7:55745200-55745201	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs7780680	chr7:55745203-55745204	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs7780681	chr7:55745205-55745206	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs7780683	chr7:55745216-55745217	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs552890670	chr7:55745268-55745269	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs577455711	chr7:55745288-55745289	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs544689943	chr7:55745310-55745311	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs35040497	chr7:55745373-55745374	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs543815540	chr7:55745419-55745420	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs200128113	chr7:55745489-55745490	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs35333847	chr7:55745517-55745518	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs144529218	chr7:55745535-55745536	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs111782661	chr7:55745540-55745541	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs561588919	chr7:55745561-55745562	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs528782256	chr7:55745615-55745616	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs540966213	chr7:55745630-55745631	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs186578572	chr7:55745696-55745697	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs532785402	chr7:55745702-55745703	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs560909019	chr7:55745710-55745711	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:88)

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
Lung cancer	18438408	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
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	21364760	CNVD
Esophageal cancer	21851588	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
small cell lung cancer	20016488	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
Glioblastoma multiforme	19115005	CNVD
Glioblastoma multiforme	21569311	CNVD
Breast cancer	17142309	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Medullary thyroid carcinoma	18765511	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	20164919	CNVD

Chromatin state (count:303 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:55729800-55730600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr7:55745200-55752600	Weak transcription	Pancreas	Pancrea
3	chr7:55745400-55745800	Enhancers	Primary neutrophils fromperipheralblood	blood
4	chr7:55750600-55750800	Bivalent Enhancer	HepG2	liver
5	chr7:55752600-55753200	Enhancers	Pancreas	Pancrea
6	chr7:55753200-55756400	Weak transcription	Pancreas	Pancrea
7	chr7:55754600-55754800	Enhancers	K562	blood
8	chr7:55754600-55757800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
9	chr7:55755400-55755800	Enhancers	Left Ventricle	heart
10	chr7:55755800-55756200	Weak transcription	Left Ventricle	heart
11	chr7:55755800-55756600	Bivalent Enhancer	HepG2	liver
12	chr7:55756000-55757400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr7:55756000-55757400	Enhancers	Fetal Lung	lung
14	chr7:55756000-55757400	Enhancers	HUVEC	blood vessel
15	chr7:55756000-55757800	Enhancers	Stomach Mucosa	stomach
16	chr7:55756000-55757800	Enhancers	NHEK	skin
17	chr7:55756200-55756800	Enhancers	Left Ventricle	heart
18	chr7:55756200-55757000	Enhancers	Primary hematopoietic stem cells	blood
19	chr7:55756200-55757400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
20	chr7:55756400-55756800	Enhancers	Ovary	ovary
21	chr7:55756400-55756800	Enhancers	Pancreas	Pancrea
22	chr7:55756400-55757000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr7:55756400-55757000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr7:55756400-55757000	Enhancers	Sigmoid Colon	Sigmoid Colon
25	chr7:55756400-55757200	Enhancers	Fetal Muscle Trunk	muscle
26	chr7:55756400-55757200	Enhancers	Rectal Mucosa Donor 29	rectum
27	chr7:55756400-55757200	Enhancers	Rectal Mucosa Donor 31	rectum
28	chr7:55756400-55757200	Enhancers	Small Intestine	intestine
29	chr7:55756400-55757200	Enhancers	Spleen	Spleen
30	chr7:55756400-55757400	Enhancers	Fetal Muscle Leg	muscle
31	chr7:55756400-55757400	Enhancers	HMEC	breast
32	chr7:55756400-55757600	Enhancers	Primary hematopoietic stem cells short term culture	blood
33	chr7:55756400-55757800	Enhancers	Cortex derived primary cultured neurospheres	brain
34	chr7:55756400-55757800	Enhancers	Colon Smooth Muscle	Colon
35	chr7:55756600-55757000	Enhancers	K562	blood
36	chr7:55756600-55757200	Enhancers	H1 Cell Line	embryonic stem cell
37	chr7:55756600-55757200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr7:55756600-55757400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
39	chr7:55756600-55757800	Enhancers	HUES6 Cell Line	embryonic stem cell
40	chr7:55756600-55757800	Enhancers	Fetal Kidney	kidney
41	chr7:55756600-55757800	Enhancers	HepG2	liver
42	chr7:55756800-55757000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
43	chr7:55756800-55757200	Enhancers	iPS-15b Cell Line	embryonic stem cell
44	chr7:55756800-55757200	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
45	chr7:55756800-55757200	Enhancers	Colonic Mucosa	Colon
46	chr7:55756800-55757200	Flanking Active TSS	Ovary	ovary
47	chr7:55756800-55757200	Flanking Active TSS	Pancreas	Pancrea
48	chr7:55756800-55757400	Enhancers	ES-I3 Cell Line	embryonic stem cell
49	chr7:55756800-55757400	Enhancers	Adipose Nuclei	Adipose
50	chr7:55756800-55757800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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