Variant report

Variant	nsv888010
Chromosome Location	chr7:48785436-48895330
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:164)
CpG islands
(count:306)
Chromatin interactive
region (count:4)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:164 , 50 per page) page: 1 2 3 4

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	chr7:48806460-48806573	A549	lung:	n/a	chr7:48806526-48806537
4	CEBPB	chr7:48795633-48795833	HepG2	liver:	n/a	chr7:48795707-48795720 chr7:48795708-48795719
5	CEBPB	chr7:48878800-48879033	HepG2	liver:	n/a	n/a
6	CEBPB	chr7:48851684-48851844	HepG2	liver:	n/a	n/a
7	CEBPB	chr7:48847193-48847277	A549	lung:	n/a	chr7:48847205-48847218
8	CEBPB	chr7:48806398-48806609	HepG2	liver:	n/a	chr7:48806526-48806537
9	CEBPB	chr7:48849803-48849906	HepG2	liver:	n/a	chr7:48849846-48849857
10	CEBPB	chr7:48872368-48872474	HepG2	liver:	n/a	n/a
11	CTCF	chr7:48806380-48806530	NHEK	skin:	n/a	n/a
12	CTCF	chr7:48882898-48882953	GM13977	blood:	n/a	n/a
13	CTCF	chr7:48854001-48854057	GM10248	blood:	n/a	n/a
14	CTCF	chr7:48884614-48884671	GM13976	blood:	n/a	n/a
15	CTCF	chr7:48788191-48788279	Fibrobl	skin:	n/a	n/a
16	CTCF	chr7:48820760-48820910	WERI-Rb-1	eye:	n/a	n/a
17	CTCF	chr7:48883318-48883365	LNCaP	prostate:	n/a	n/a
18	CTCF	chr7:48893527-48893532	Fibrobl	skin:	n/a	n/a
19	CTCF	chr7:48819740-48819890	GM06990	blood:	n/a	n/a
20	CTCF	chr7:48788287-48788296	ProgFib	skin:	n/a	n/a
21	CTCF	chr7:48788237-48788283	ProgFib	skin:	n/a	n/a
22	CTCF	chr7:48787855-48787859	MCF-7	breast:	n/a	n/a
23	CTCF	chr7:48793050-48793067	Medullo	brain:	n/a	n/a
24	CTCF	chr7:48883292-48883299	LNCaP	prostate:	n/a	n/a
25	CTCF	chr7:48884571-48884667	Lung_OC	lung:	n/a	n/a
26	CTCF	chr7:48797822-48797858	Spleen_OC	spleen:	n/a	n/a
27	CTCF	chr7:48820680-48820830	NHEK	skin:	n/a	n/a
28	CTCF	chr7:48787861-48787868	MCF-7	breast:	n/a	n/a
29	CTCF	chr7:48887972-48888033	Kidney_OC	kidney:	n/a	n/a
30	CUX1	chr7:48803302-48803345	GM12878	blood:	n/a	n/a
31	CUX1	chr7:48843568-48843650	GM12878	blood:	n/a	n/a
32	E2F4	chr7:48854521-48854657	MCF10A-Er-Src	breast:	n/a	n/a
33	E2F4	chr7:48851550-48851727	MCF10A-Er-Src	breast:	n/a	chr7:48851695-48851712
34	E2F4	chr7:48869122-48869273	MCF10A-Er-Src	breast:	n/a	n/a
35	E2F4	chr7:48835785-48835821	MCF10A-Er-Src	breast:	n/a	n/a
36	EBF1	chr7:48821428-48821623	GM12878	blood:	n/a	n/a
37	EBF1	chr7:48821913-48822098	GM12878	blood:	n/a	n/a
38	EBF1	chr7:48821359-48821673	GM12878	blood:	n/a	n/a
39	EP300	chr7:48788041-48788106	GM12878	blood:	n/a	n/a
40	FOS	chr7:48878719-48879065	MCF10A-Er-Src	breast:	n/a	chr7:48878884-48878892
41	FOS	chr7:48878716-48879075	MCF10A-Er-Src	breast:	n/a	chr7:48878884-48878892
42	FOS	chr7:48878703-48879104	MCF10A-Er-Src	breast:	n/a	chr7:48878884-48878892
43	FOS	chr7:48878719-48879080	MCF10A-Er-Src	breast:	n/a	chr7:48878884-48878892
44	FOS	chr7:48875314-48875504	MCF10A-Er-Src	breast:	n/a	n/a
45	FOS	chr7:48875424-48875476	MCF10A-Er-Src	breast:	n/a	n/a
46	FOSL2	chr7:48884985-48885221	HepG2	liver:	n/a	chr7:48885209-48885217 chr7:48885210-48885217
47	FOXA1	chr7:48813570-48813830	T-47D	breast:	n/a	n/a
48	FOXA1	chr7:48822216-48822469	T-47D	breast:	n/a	n/a
49	FOXA1	chr7:48813473-48813910	T-47D	breast:	n/a	n/a
50	GATA3	chr7:48841700-48841900	SH-SY5Y	brain:	n/a	n/a

(count:306 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:48887421-48887471	K562	blood:	n/a
2	chr7:48887421-48887471	K562	blood:	n/a
3	chr7:48884523-48884573	PFSK-1	brain:	n/a
4	chr7:48887421-48887471	AG04449	skin:	fetal
5	chr7:48887640-48887690	HCF	heart:	n/a
6	chr7:48887585-48887635	HRE	kidney:	n/a
7	chr7:48887585-48887635	HCPEpiC	choroid plexus:	n/a
8	chr7:48887585-48887635	MCF10A-Er-Src	breast:	n/a
9	chr7:48887640-48887690	SK-N-MC	brain:	n/a
10	chr7:48887640-48887690	AG09309	skin:	n/a
11	chr7:48889641-48889691	MCF10A-Er-Src	breast:	n/a
12	chr7:48889641-48889691	HL-60	blood:	n/a
13	chr7:48884523-48884573	SK-N-SH	brain:	n/a
14	chr7:48889641-48889691	NH-A	brain:	n/a
15	chr7:48884523-48884573	K562	blood:	n/a
16	chr7:48884523-48884573	HUVEC	blood vessel:	n/a
17	chr7:48887585-48887635	ECC-1	luminal epithelium:	n/a
18	chr7:48887585-48887635	LNCaP	prostate:	n/a
19	chr7:48884523-48884573	NHDF-neo	bronchial:	n/a
20	chr7:48889641-48889691	U87	brain:	n/a
21	chr7:48887421-48887471	A549	lung:	n/a
22	chr7:48887421-48887471	CMK	blood:	n/a
23	chr7:48884523-48884573	SAEC	small airway:	n/a
24	chr7:48887640-48887690	NT2-D1	testis:	n/a
25	chr7:48887585-48887635	HNPCEpiC	eye:	n/a
26	chr7:48889641-48889691	ProgFib	skin:	n/a
27	chr7:48887585-48887635	HRPEpiC	eye:	n/a
28	chr7:48887585-48887635	Jurkat	blood:	n/a
29	chr7:48887585-48887635	NH-A	brain:	n/a
30	chr7:48887640-48887690	AG09319	gingival:	n/a
31	chr7:48887421-48887471	NB4	blood:	n/a
32	chr7:48884523-48884573	SK-N-SH_RA	brain:	n/a
33	chr7:48889641-48889691	HIPEpiC	eye:	n/a
34	chr7:48887640-48887690	SK-N-SH	brain:	n/a
35	chr7:48887421-48887471	AG09319	gingival:	n/a
36	chr7:48884523-48884573	SK-N-MC	brain:	n/a
37	chr7:48884523-48884573	ECC-1	luminal epithelium:	n/a
38	chr7:48889641-48889691	LNCaP	prostate:	n/a
39	chr7:48884523-48884573	HCM	heart:	n/a
40	chr7:48887640-48887690	K562	blood:	n/a
41	chr7:48889641-48889691	GM12891	blood:	n/a
42	chr7:48884523-48884573	ovcar-3	ovarian:	n/a
43	chr7:48884523-48884573	GM12891	blood:	n/a
44	chr7:48887421-48887471	Hela-S3	cervix:	n/a
45	chr7:48887640-48887690	ovcar-3	ovarian:	n/a
46	chr7:48889641-48889691	GM12892	blood:	n/a
47	chr7:48887640-48887690	HAEpiC	amniotic membrane:	n/a
48	chr7:48889641-48889691	HepG2	liver:	n/a
49	chr7:48887421-48887471	HCM	heart:	n/a
50	chr7:48887421-48887471	T-47D	breast:	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	chr7:48350873..48351428-chr7:48826215..48827185,2	MCF-7	breast:
3	chr7:48882427..48884923-chr7:49456665..49458198,2	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-ABCA13-3	chr7:48854078-48854124	l_3412_chr7:48854077-48855837_testes
2	lnc-ABCA13-2	chr7:48883532-48883578	XLOC_006092
3	lnc-ABCA13-3	chr7:48855232-48855837	l_3412_chr7:48854077-48855837_testes
4	lnc-ABCA13-2	chr7:48884686-48885282	XLOC_006092

No data

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

Extended variants
information (count: 930 )
Associated
traits (count: 122 )

Variant overlapped rSNPs/rCNVs (count:930 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11976931	chr7:48787602-48787603	Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs148129072	chr7:48787614-48787615	Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs556621306	chr7:48787636-48787637	Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs2082825	chr7:48787644-48787645	Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs553352056	chr7:48787647-48787648	Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs573641063	chr7:48787648-48787649	Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs141052400	chr7:48787684-48787685	Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs111577539	chr7:48787687-48787688	Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs531420050	chr7:48787711-48787712	Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs545170524	chr7:48787718-48787719	Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs113148573	chr7:48787743-48787744	Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs116337616	chr7:48787755-48787756	Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs184078623	chr7:48787773-48787774	Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs146496546	chr7:48787783-48787784	Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs59404141	chr7:48787790-48787791	Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs113296068	chr7:48787836-48787837	Enhancers Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs6969167	chr7:48787850-48787851	Enhancers Active TSS ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs570297239	chr7:48787881-48787882	Enhancers Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs188858871	chr7:48787885-48787886	Enhancers Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs552333133	chr7:48787897-48787898	Enhancers Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs139115861	chr7:48787905-48787906	Enhancers Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs533634392	chr7:48787928-48787929	Enhancers Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs112709805	chr7:48787939-48787940	Enhancers Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs180844292	chr7:48787940-48787941	Enhancers Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs536208676	chr7:48787952-48787953	Enhancers Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs556217228	chr7:48787976-48787977	Enhancers Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs185337412	chr7:48788013-48788014	Active TSS Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs77896148	chr7:48788017-48788018	Active TSS Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs544919811	chr7:48788117-48788118	Active TSS Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs565064229	chr7:48788122-48788123	Active TSS Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs572229224	chr7:48788124-48788125	Active TSS Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs191788260	chr7:48788125-48788126	Active TSS Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs376804120	chr7:48788144-48788145	Active TSS Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs182464384	chr7:48788161-48788162	Active TSS Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs143145053	chr7:48788163-48788164	Active TSS Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs550134012	chr7:48788180-48788181	Active TSS Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs563856968	chr7:48788206-48788207	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs377292345	chr7:48788230-48788231	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs532839160	chr7:48788234-48788235	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs552398373	chr7:48788240-48788241	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs147454253	chr7:48788247-48788248	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs534858677	chr7:48788257-48788258	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs73098500	chr7:48788301-48788302	Flanking Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs567338033	chr7:48788323-48788324	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs535895730	chr7:48788329-48788330	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs556120273	chr7:48788336-48788337	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs74527026	chr7:48788367-48788368	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs538943569	chr7:48788376-48788377	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs191755709	chr7:48788402-48788403	Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs375711611	chr7:48788406-48788407	Active TSS	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:71 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:48787600-48788000	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr7:48787800-48788200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr7:48787800-48788200	ZNF genes & repeats	Pancreas	Pancrea
4	chr7:48788000-48788200	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr7:48788000-48788400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr7:48788200-48788400	Flanking Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr7:48788200-48788400	Flanking Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr7:48788400-48788800	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr7:48793400-48794400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
10	chr7:48793400-48794400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr7:48793600-48794800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr7:48794000-48794200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
13	chr7:48794200-48795400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
14	chr7:48794400-48795200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr7:48794400-48795200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr7:48794800-48795200	Enhancers	Breast Myoepithelial Primary Cells	Breast
17	chr7:48795200-48795400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr7:48795400-48796400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
19	chr7:48798200-48799000	Enhancers	HUES64 Cell Line	embryonic stem cell
20	chr7:48798800-48799200	Enhancers	iPS-18 Cell Line	embryonic stem cell
21	chr7:48800400-48801000	Enhancers	HSMMtube	muscle
22	chr7:48821400-48821600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr7:48821600-48822400	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr7:48821800-48822200	Enhancers	NH-A	brain
25	chr7:48822000-48822200	Enhancers	Adipose Nuclei	Adipose
26	chr7:48822400-48822600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr7:48826600-48827000	Enhancers	Esophagus	oesophagus
28	chr7:48826800-48827200	Enhancers	Brain Germinal Matrix	brain
29	chr7:48826800-48827400	Enhancers	Breast Myoepithelial Primary Cells	Breast
30	chr7:48833000-48833200	Weak transcription	Pancreas	Pancrea
31	chr7:48833200-48833400	ZNF genes & repeats	Pancreas	Pancrea
32	chr7:48833400-48836400	Weak transcription	Pancreas	Pancrea
33	chr7:48850400-48850800	Enhancers	Primary T cells from cord blood	blood
34	chr7:48850400-48851400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr7:48850400-48851400	Enhancers	Breast Myoepithelial Primary Cells	Breast
36	chr7:48850800-48851200	Weak transcription	Primary T cells from cord blood	blood
37	chr7:48851200-48851400	Enhancers	Primary T cells from cord blood	blood
38	chr7:48851400-48852400	Weak transcription	Primary T cells from cord blood	blood
39	chr7:48852400-48853400	Enhancers	Primary T cells from cord blood	blood
40	chr7:48852600-48853400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr7:48857200-48858000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
42	chr7:48871200-48872800	Enhancers	Brain Angular Gyrus	brain
43	chr7:48871600-48872000	Enhancers	Brain Hippocampus Middle	brain
44	chr7:48871600-48872800	Enhancers	Brain Inferior Temporal Lobe	brain
45	chr7:48871800-48872800	Enhancers	Brain Substantia Nigra	brain
46	chr7:48872000-48872400	Flanking Active TSS	Brain Cingulate Gyrus	brain
47	chr7:48872000-48872400	Flanking Active TSS	Brain Hippocampus Middle	brain
48	chr7:48872000-48872800	Enhancers	Brain Anterior Caudate	brain
49	chr7:48872200-48872800	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
50	chr7:48872400-48872800	Enhancers	Brain Cingulate Gyrus	brain

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