Variant report

Variant	nsv888011
Chromosome Location	chr7:48809570-48894689
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:125)
CpG islands
(count:305)
Chromatin interactive
region (count:4)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:125 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BCL11A	chr7:48821475-48821666	GM12878	blood:	n/a	n/a
2	BRCA1	chr7:48829561-48829585	GM12878	blood:	n/a	n/a
3	CEBPB	chr7:48849803-48849906	HepG2	liver:	n/a	chr7:48849846-48849857
4	CEBPB	chr7:48847193-48847277	A549	lung:	n/a	chr7:48847205-48847218
5	CEBPB	chr7:48851684-48851844	HepG2	liver:	n/a	n/a
6	CEBPB	chr7:48872368-48872474	HepG2	liver:	n/a	n/a
7	CEBPB	chr7:48878800-48879033	HepG2	liver:	n/a	n/a
8	CTCF	chr7:48854001-48854057	GM10248	blood:	n/a	n/a
9	CTCF	chr7:48883292-48883299	LNCaP	prostate:	n/a	n/a
10	CTCF	chr7:48887972-48888033	Kidney_OC	kidney:	n/a	n/a
11	CTCF	chr7:48884571-48884667	Lung_OC	lung:	n/a	n/a
12	CTCF	chr7:48883318-48883365	LNCaP	prostate:	n/a	n/a
13	CTCF	chr7:48882898-48882953	GM13977	blood:	n/a	n/a
14	CTCF	chr7:48820760-48820910	WERI-Rb-1	eye:	n/a	n/a
15	CTCF	chr7:48820680-48820830	NHEK	skin:	n/a	n/a
16	CTCF	chr7:48884614-48884671	GM13976	blood:	n/a	n/a
17	CTCF	chr7:48893527-48893532	Fibrobl	skin:	n/a	n/a
18	CTCF	chr7:48819740-48819890	GM06990	blood:	n/a	n/a
19	CUX1	chr7:48843568-48843650	GM12878	blood:	n/a	n/a
20	E2F4	chr7:48854521-48854657	MCF10A-Er-Src	breast:	n/a	n/a
21	E2F4	chr7:48869122-48869273	MCF10A-Er-Src	breast:	n/a	n/a
22	E2F4	chr7:48835785-48835821	MCF10A-Er-Src	breast:	n/a	n/a
23	E2F4	chr7:48851550-48851727	MCF10A-Er-Src	breast:	n/a	chr7:48851695-48851712
24	EBF1	chr7:48821359-48821673	GM12878	blood:	n/a	n/a
25	EBF1	chr7:48821428-48821623	GM12878	blood:	n/a	n/a
26	EBF1	chr7:48821913-48822098	GM12878	blood:	n/a	n/a
27	FOS	chr7:48875424-48875476	MCF10A-Er-Src	breast:	n/a	n/a
28	FOS	chr7:48878719-48879080	MCF10A-Er-Src	breast:	n/a	chr7:48878884-48878892
29	FOS	chr7:48878716-48879075	MCF10A-Er-Src	breast:	n/a	chr7:48878884-48878892
30	FOS	chr7:48878719-48879065	MCF10A-Er-Src	breast:	n/a	chr7:48878884-48878892
31	FOS	chr7:48878703-48879104	MCF10A-Er-Src	breast:	n/a	chr7:48878884-48878892
32	FOS	chr7:48875314-48875504	MCF10A-Er-Src	breast:	n/a	n/a
33	FOSL2	chr7:48884985-48885221	HepG2	liver:	n/a	chr7:48885209-48885217 chr7:48885210-48885217
34	FOXA1	chr7:48822216-48822469	T-47D	breast:	n/a	n/a
35	FOXA1	chr7:48813570-48813830	T-47D	breast:	n/a	n/a
36	FOXA1	chr7:48813473-48813910	T-47D	breast:	n/a	n/a
37	GATA3	chr7:48827919-48828205	T-47D	breast:	n/a	n/a
38	GATA3	chr7:48821997-48822413	T-47D	breast:	n/a	n/a
39	GATA3	chr7:48827928-48828181	T-47D	breast:	n/a	n/a
40	GATA3	chr7:48855199-48855384	SH-SY5Y	brain:	n/a	n/a
41	GATA3	chr7:48841700-48841900	SH-SY5Y	brain:	n/a	n/a
42	GATA3	chr7:48813516-48813962	T-47D	breast:	n/a	n/a
43	GATA3	chr7:48827613-48827912	T-47D	breast:	n/a	n/a
44	GATA3	chr7:48843257-48843597	SH-SY5Y	brain:	n/a	n/a
45	IRF1	chr7:48809533-48809692	K562	blood:	n/a	n/a
46	JUN	chr7:48814121-48814228	H1-hESC	embryonic stem cell:	n/a	n/a
47	JUND	chr7:48829863-48830146	HepG2	liver:	n/a	chr7:48829980-48829989
48	JUND	chr7:48878817-48879010	HepG2	liver:	n/a	chr7:48878882-48878893 chr7:48878884-48878892
49	MAFF	chr7:48814716-48814993	HepG2	liver:	n/a	chr7:48814859-48814877
50	MAFF	chr7:48850852-48851142	HepG2	liver:	n/a	n/a

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:48887585-48887635	PANC-1	pancreas:	n/a
2	chr7:48889641-48889691	AG09319	gingival:	n/a
3	chr7:48887640-48887690	ECC-1	luminal epithelium:	n/a
4	chr7:48887585-48887635	HCF	heart:	n/a
5	chr7:48884523-48884573	GM19239	blood:	n/a
6	chr7:48887585-48887635	HIPEpiC	eye:	n/a
7	chr7:48887640-48887690	HAEpiC	amniotic membrane:	n/a
8	chr7:48884523-48884573	AG10803	skin:	n/a
9	chr7:48887640-48887690	SK-N-MC	brain:	n/a
10	chr7:48887421-48887471	H1-hESC	embryonic stem cell:	embryo
11	chr7:48889641-48889691	GM12892	blood:	n/a
12	chr7:48884523-48884573	GM12878	blood:	n/a
13	chr7:48889641-48889691	LNCaP	prostate:	n/a
14	chr7:48887421-48887471	CMK	blood:	n/a
15	chr7:48887585-48887635	HAEpiC	amniotic membrane:	n/a
16	chr7:48889641-48889691	PFSK-1	brain:	n/a
17	chr7:48887585-48887635	HRPEpiC	eye:	n/a
18	chr7:48887585-48887635	U87	brain:	n/a
19	chr7:48889641-48889691	MCF-7	breast:	n/a
20	chr7:48889641-48889691	AG04450	lung:	fetal
21	chr7:48889641-48889691	ovcar-3	ovarian:	n/a
22	chr7:48889641-48889691	HL-60	blood:	n/a
23	chr7:48887640-48887690	RPTEC	kidney:	n/a
24	chr7:48884523-48884573	GM06990	blood:	n/a
25	chr7:48887421-48887471	K562	blood:	n/a
26	chr7:48884523-48884573	HAEpiC	amniotic membrane:	n/a
27	chr7:48887640-48887690	MCF10A-Er-Src	breast:	n/a
28	chr7:48887421-48887471	IMR90	lung:	fetal
29	chr7:48889641-48889691	HepG2	liver:	n/a
30	chr7:48887585-48887635	HCPEpiC	choroid plexus:	n/a
31	chr7:48884523-48884573	NH-A	brain:	n/a
32	chr7:48887640-48887690	IMR90	lung:	fetal
33	chr7:48887421-48887471	HCPEpiC	choroid plexus:	n/a
34	chr7:48889641-48889691	HCT-116	colon:	n/a
35	chr7:48887421-48887471	SK-N-MC	brain:	n/a
36	chr7:48889641-48889691	PrEC	prostate:	n/a
37	chr7:48884523-48884573	MCF10A-Er-Src	breast:	n/a
38	chr7:48887640-48887690	HCPEpiC	choroid plexus:	n/a
39	chr7:48884523-48884573	SK-N-SH	brain:	n/a
40	chr7:48884523-48884573	HPAEpiC	pulmonary alveolar:	n/a
41	chr7:48884523-48884573	HUVEC	blood vessel:	n/a
42	chr7:48887585-48887635	MCF-7	breast:	n/a
43	chr7:48887585-48887635	HRE	kidney:	n/a
44	chr7:48887421-48887471	HIPEpiC	eye:	n/a
45	chr7:48884523-48884573	SK-N-MC	brain:	n/a
46	chr7:48887640-48887690	BE2_C	brain:	n/a
47	chr7:48887640-48887690	PANC-1	pancreas:	n/a
48	chr7:48884523-48884573	HEEpiC	esophagus:	n/a
49	chr7:48884523-48884573	HNPCEpiC	eye:	n/a
50	chr7:48887421-48887471	ECC-1	luminal epithelium:	n/a

(count:4 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:48863351..48865401-chr7:48869144..48870913,2	K562	blood:
2	chr7:48882427..48884923-chr7:49456665..49458198,2	MCF-7	breast:
3	chr7:48350873..48351428-chr7:48826215..48827185,2	MCF-7	breast:
4	chr7:48863351..48865401-chr7:48869144..48870913,2	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ABCA13-2	chr7:48884686-48885282	XLOC_006092
2	lnc-ABCA13-3	chr7:48854078-48854124	l_3412_chr7:48854077-48855837_testes
3	lnc-ABCA13-3	chr7:48855232-48855837	l_3412_chr7:48854077-48855837_testes
4	lnc-ABCA13-2	chr7:48883532-48883578	XLOC_006092

No data

Variant related genes	Relation type
ENSG00000267970	TF binding region
ENSG00000225705	TF binding region
ENSG00000267970	CpG island
ENSG00000225705	CpG island

Extended variants
information (count: 687 )
Associated
traits (count: 122 )

Variant overlapped rSNPs/rCNVs (count:687 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs548905950	chr7:48821441-48821442	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs562241872	chr7:48821451-48821452	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs531184735	chr7:48821516-48821517	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs191031703	chr7:48821526-48821527	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs73696955	chr7:48821527-48821528	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs371528786	chr7:48821528-48821529	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs561732218	chr7:48821529-48821530	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs551969108	chr7:48821538-48821539	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs565707739	chr7:48821542-48821543	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs150920569	chr7:48821593-48821594	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs554499511	chr7:48821627-48821628	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs574400043	chr7:48821662-48821663	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs183195561	chr7:48821703-48821704	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs556762121	chr7:48821711-48821712	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs140816347	chr7:48821714-48821715	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs553886042	chr7:48821765-48821766	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs116603030	chr7:48821770-48821771	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs372151202	chr7:48821785-48821786	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs559583994	chr7:48821788-48821789	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs138470519	chr7:48821794-48821795	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs541860965	chr7:48821803-48821804	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs113408305	chr7:48821835-48821836	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs531253722	chr7:48821851-48821852	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs530896436	chr7:48821894-48821895	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs375217796	chr7:48821896-48821897	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs551273449	chr7:48821929-48821930	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs113275756	chr7:48821949-48821950	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs564703278	chr7:48821972-48821973	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs541958128	chr7:48821976-48821977	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs112976169	chr7:48821999-48822000	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs563864036	chr7:48822005-48822006	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs191268043	chr7:48822016-48822017	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs375831205	chr7:48822034-48822035	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs183759613	chr7:48822035-48822036	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs567692936	chr7:48822057-48822058	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs187564115	chr7:48822104-48822105	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs556823549	chr7:48822124-48822125	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs576668986	chr7:48822134-48822135	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs539255567	chr7:48822202-48822203	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs553085852	chr7:48822256-48822257	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs531178605	chr7:48822263-48822264	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs573266444	chr7:48822294-48822295	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs533785528	chr7:48822295-48822296	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs369303631	chr7:48822300-48822301	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs542279926	chr7:48822322-48822323	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs116826037	chr7:48822327-48822328	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs141469710	chr7:48822369-48822370	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs192595148	chr7:48822386-48822387	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs114543808	chr7:48822416-48822417	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs371556401	chr7:48822435-48822436	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:122)

Disease	PMID	Source
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Biliary cancer	19435499	CNVD
Wilms tumour	21544195	CNVD
Neuroblastoma	18923191	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
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
lymphocytic leukemia	21291569	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Cancer	21637783	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16397240	CNVD
Non-small cell lung cancer	21829676	CNVD
Glioblastoma multiforme	17002787	CNVD
Autism	22495311	CNVD
Glioblastoma multiforme	18628472	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Follicular lymphoma	20505157	CNVD
Williams-beuren syndrome	22470819	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21364760	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21750150	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute myeloid leukemia	17237825	CNVD
Gastric cancer	24379144	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Abnormal phenotypes	18644119	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Esophageal cancer	21851588	CNVD
Lung adenocarcinoma	17086460	CNVD
Lung cancer	17086460	CNVD
Non-small cell lung cancer	17643093	CNVD
Ovarian cancer	18182111	CNVD
Colorectal cancer	16272173	CNVD
Glioblastoma multiforme	17369134	CNVD
Barrett''s esophagus	18559552	CNVD
head and neck squamous cell carcinoma	16943533	CNVD
Anaplastic thyroid cancer	17079354	CNVD
Basal-like breast cancer	17875215	CNVD
Colorectal cancer	16882699	CNVD
Colorectal cancer	18794099	CNVD
Gastrointestinal stromal cancer	17643098	CNVD
Lung cancer	18381415	CNVD
Metastatic colorectal cancer	17664472	CNVD
Non-small cell lung cancer	19255323	CNVD
Non-small cell lung cancer	17673923	CNVD
Non-small cell lung cancer	17975165	CNVD
Non-small cell lung cancer	19622585	CNVD
Ovarian cancer	16607561	CNVD
Squamous cell cancer	19670535	CNVD
head and neck squamous cell carcinoma	16818711	CNVD
small cell lung cancer	18829487	CNVD
Breast cancer	17661082	CNVD
Adenocarcinoma	19260752	CNVD
Esophageal cancer	16575012	CNVD
Lung adenocarcinoma	19138956	CNVD
Lung adenocarcinoma	18379350	CNVD
Lung adenocarcinoma	18258923	CNVD
Lung cancer	19138956	CNVD
Lung cancer	18379350	CNVD
Lung cancer	18258923	CNVD
Non-small cell lung cancer	18304967	CNVD
Non-small cell lung cancer	19451690	CNVD
Non-small cell lung cancer	19260752	CNVD
Non-small cell lung cancer	17079354	CNVD
Non-small cell lung cancer	18559607	CNVD
Rectal cancer	19506820	CNVD
Triple-negative breast cancer	18950515	CNVD
head and neck squamous cell carcinoma	18813952	CNVD
Non-small cell lung cancer	17504988	CNVD
Non-small cell lung cancer	16943533	CNVD
Non-small cell lung cancer	18509184	CNVD
head and neck squamous cell carcinoma	17538160	CNVD
Colorectal cancer	19712476	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Lung cancer	19671679	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	16864856	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:48821400-48821600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr7:48821600-48822400	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr7:48821800-48822200	Enhancers	NH-A	brain
4	chr7:48822000-48822200	Enhancers	Adipose Nuclei	Adipose
5	chr7:48822400-48822600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr7:48826600-48827000	Enhancers	Esophagus	oesophagus
7	chr7:48826800-48827200	Enhancers	Brain Germinal Matrix	brain
8	chr7:48826800-48827400	Enhancers	Breast Myoepithelial Primary Cells	Breast
9	chr7:48833000-48833200	Weak transcription	Pancreas	Pancrea
10	chr7:48833200-48833400	ZNF genes & repeats	Pancreas	Pancrea
11	chr7:48833400-48836400	Weak transcription	Pancreas	Pancrea
12	chr7:48850400-48850800	Enhancers	Primary T cells from cord blood	blood
13	chr7:48850400-48851400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr7:48850400-48851400	Enhancers	Breast Myoepithelial Primary Cells	Breast
15	chr7:48850800-48851200	Weak transcription	Primary T cells from cord blood	blood
16	chr7:48851200-48851400	Enhancers	Primary T cells from cord blood	blood
17	chr7:48851400-48852400	Weak transcription	Primary T cells from cord blood	blood
18	chr7:48852400-48853400	Enhancers	Primary T cells from cord blood	blood
19	chr7:48852600-48853400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr7:48857200-48858000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
21	chr7:48871200-48872800	Enhancers	Brain Angular Gyrus	brain
22	chr7:48871600-48872000	Enhancers	Brain Hippocampus Middle	brain
23	chr7:48871600-48872800	Enhancers	Brain Inferior Temporal Lobe	brain
24	chr7:48871800-48872800	Enhancers	Brain Substantia Nigra	brain
25	chr7:48872000-48872400	Flanking Active TSS	Brain Cingulate Gyrus	brain
26	chr7:48872000-48872400	Flanking Active TSS	Brain Hippocampus Middle	brain
27	chr7:48872000-48872800	Enhancers	Brain Anterior Caudate	brain
28	chr7:48872200-48872800	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
29	chr7:48872400-48872800	Enhancers	Brain Cingulate Gyrus	brain
30	chr7:48872400-48872800	Enhancers	Brain Hippocampus Middle	brain
31	chr7:48876800-48877400	Enhancers	Fetal Heart	heart
32	chr7:48878600-48879200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr7:48878600-48879200	Enhancers	Breast Myoepithelial Primary Cells	Breast
34	chr7:48878600-48879400	Enhancers	Esophagus	oesophagus
35	chr7:48878600-48879400	Enhancers	HMEC	breast
36	chr7:48884600-48885000	Enhancers	Adipose Nuclei	Adipose
37	chr7:48887400-48887600	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr7:48887400-48887600	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
39	chr7:48887400-48887600	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
40	chr7:48887400-48887600	Bivalent/Poised TSS	Fetal Intestine Small	intestine
41	chr7:48887400-48887800	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
42	chr7:48887400-48888000	Active TSS	Brain Germinal Matrix	brain
43	chr7:48887400-48888000	Active TSS	Right Ventricle	heart
44	chr7:48887600-48887800	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr7:48887600-48887800	Bivalent/Poised TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
46	chr7:48887600-48887800	Flanking Bivalent TSS/Enh	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr7:48887600-48887800	Enhancers	Left Ventricle	heart
48	chr7:48887600-48887800	Enhancers	Pancreas	Pancrea
49	chr7:48887600-48887800	Enhancers	Psoas Muscle	Psoas
50	chr7:48887600-48888000	Bivalent/Poised TSS	Foreskin Keratinocyte Primary Cells skin03	Skin

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