Variant report

Variant	nsv970558
Chromosome Location	chr7:99358519-99389907
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:188)
CpG islands
(count:305)
Chromatin interactive
region (count:8)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:188 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:99370143-99370615	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:99364310-99364654	K562	blood:	n/a	n/a
3	ATF2	chr7:99365248-99365724	GM12878	blood:	n/a	n/a
4	ATF2	chr7:99365148-99365713	GM12878	blood:	n/a	n/a
5	BATF	chr7:99365239-99365549	GM12878	blood:	n/a	n/a
6	BATF	chr7:99365247-99365623	GM12878	blood:	n/a	n/a
7	BCL11A	chr7:99365231-99365629	GM12878	blood:	n/a	n/a
8	BHLHE40	chr7:99366245-99366383	GM12878	blood:	n/a	n/a
9	BHLHE40	chr7:99360674-99360886	K562	blood:	n/a	n/a
10	BHLHE40	chr7:99365355-99365633	GM12878	blood:	n/a	n/a
11	CBX3	chr7:99360292-99360970	K562	blood:	n/a	n/a
12	CEBPB	chr7:99389792-99389980	K562	blood:	n/a	n/a
13	CEBPB	chr7:99370297-99370473	HepG2	liver:	n/a	n/a
14	CEBPB	chr7:99370271-99370552	HepG2	liver:	n/a	n/a
15	CEBPB	chr7:99387454-99387676	HepG2	liver:	n/a	chr7:99387500-99387511
16	CEBPB	chr7:99389868-99389875	HepG2	liver:	n/a	n/a
17	CEBPB	chr7:99360356-99360612	K562	blood:	n/a	n/a
18	CHD2	chr7:99365347-99365565	GM12878	blood:	n/a	n/a
19	CTCF	chr7:99379940-99380090	HMEC	breast:	n/a	n/a
20	CTCF	chr7:99380003-99380091	HepG2	liver:	n/a	n/a
21	CTCF	chr7:99379960-99380110	HEK293	kidney:	n/a	n/a
22	CTCF	chr7:99379980-99380130	MCF-7	breast:	n/a	n/a
23	CTCF	chr7:99380023-99380072	Hela-S3	cervix:	n/a	n/a
24	CTCF	chr7:99379520-99379670	GM12869	blood:	n/a	n/a
25	CTCF	chr7:99379900-99380050	GM12872	blood:	n/a	n/a
26	CTCF	chr7:99379926-99380103	HepG2	liver:	n/a	n/a
27	CTCF	chr7:99379980-99380130	K562	blood:	n/a	n/a
28	CTCF	chr7:99379946-99380130	K562	blood:	n/a	n/a
29	CTCF	chr7:99379940-99380090	HepG2	liver:	n/a	n/a
30	CTCF	chr7:99379920-99380070	RPTEC	kidney:	n/a	n/a
31	CTCF	chr7:99379904-99380157	K562	blood:	n/a	n/a
32	CUX1	chr7:99360597-99361175	K562	blood:	n/a	n/a
33	CUX1	chr7:99365256-99365588	GM12878	blood:	n/a	n/a
34	EBF1	chr7:99365230-99365634	GM12878	blood:	n/a	chr7:99365456-99365467
35	EBF1	chr7:99360832-99361020	GM12878	blood:	n/a	n/a
36	EBF1	chr7:99365268-99365651	GM12878	blood:	n/a	chr7:99365456-99365467
37	EBF1	chr7:99361696-99361858	GM12878	blood:	n/a	n/a
38	EBF1	chr7:99365165-99365749	GM12878	blood:	n/a	chr7:99365456-99365467
39	EGR1	chr7:99386208-99386463	K562	blood:	n/a	chr7:99386359-99386370 chr7:99386357-99386372
40	ELF1	chr7:99370237-99370540	HepG2	liver:	n/a	n/a
41	ELK1	chr7:99365390-99365532	GM12878	blood:	n/a	n/a
42	EP300	chr7:99370182-99370601	HepG2	liver:	n/a	chr7:99370459-99370466
43	EP300	chr7:99360387-99360956	K562	blood:	n/a	n/a
44	EP300	chr7:99365314-99365626	GM12878	blood:	n/a	n/a
45	EP300	chr7:99370150-99370588	HepG2	liver:	n/a	chr7:99370459-99370466
46	EP300	chr7:99365290-99365561	GM12878	blood:	n/a	n/a
47	EP300	chr7:99364259-99364654	Hela-S3	cervix:	n/a	n/a
48	FOS	chr7:99364501-99364720	MCF10A-Er-Src	breast:	n/a	chr7:99364555-99364563 chr7:99364556-99364567 chr7:99364553-99364565
49	FOS	chr7:99387403-99387589	MCF10A-Er-Src	breast:	n/a	n/a
50	FOS	chr7:99377694-99377823	MCF10A-Er-Src	breast:	n/a	chr7:99377769-99377776 chr7:99377767-99377776 chr7:99377768-99377777 chr7:99377766-99377778 chr7:99377768-99377776

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:99382086-99382136	H1-hESC	embryonic stem cell:	embryo
2	chr7:99383224-99383274	RPTEC	kidney:	n/a
3	chr7:99382086-99382136	GM12892	blood:	n/a
4	chr7:99382370-99382420	HAEpiC	amniotic membrane:	n/a
5	chr7:99382370-99382420	AG09319	gingival:	n/a
6	chr7:99383224-99383274	HMEC	breast:	n/a
7	chr7:99376495-99376545	AG04449	skin:	fetal
8	chr7:99382370-99382420	SKMC	muscle:	n/a
9	chr7:99383224-99383274	HCT-116	colon:	n/a
10	chr7:99382370-99382420	HEEpiC	esophagus:	n/a
11	chr7:99382086-99382136	PANC-1	pancreas:	n/a
12	chr7:99376495-99376545	HEK293	kidney:	embryo
13	chr7:99382370-99382420	MCF-7	breast:	n/a
14	chr7:99376495-99376545	H1-hESC	embryonic stem cell:	embryo
15	chr7:99383224-99383274	HUVEC	blood vessel:	n/a
16	chr7:99383155-99383205	HEEpiC	esophagus:	n/a
17	chr7:99382370-99382420	HCPEpiC	choroid plexus:	n/a
18	chr7:99382086-99382136	SK-N-SH_RA	brain:	n/a
19	chr7:99382370-99382420	HRPEpiC	eye:	n/a
20	chr7:99383155-99383205	PrEC	prostate:	n/a
21	chr7:99383224-99383274	SKMC	muscle:	n/a
22	chr7:99383155-99383205	LNCaP	prostate:	n/a
23	chr7:99382086-99382136	HRPEpiC	eye:	n/a
24	chr7:99383155-99383205	HUVEC	blood vessel:	n/a
25	chr7:99383224-99383274	Hela-S3	cervix:	n/a
26	chr7:99376495-99376545	AG09319	gingival:	n/a
27	chr7:99376495-99376545	MCF10A-Er-Src	breast:	n/a
28	chr7:99382086-99382136	HCF	heart:	n/a
29	chr7:99383155-99383205	SKMC	muscle:	n/a
30	chr7:99376495-99376545	HCM	heart:	n/a
31	chr7:99382370-99382420	RPTEC	kidney:	n/a
32	chr7:99383224-99383274	HEK293	kidney:	embryo
33	chr7:99383155-99383205	U87	brain:	n/a
34	chr7:99383224-99383274	HEEpiC	esophagus:	n/a
35	chr7:99376495-99376545	GM19239	blood:	n/a
36	chr7:99383155-99383205	K562	blood:	n/a
37	chr7:99376495-99376545	HNPCEpiC	eye:	n/a
38	chr7:99382370-99382420	HCM	heart:	n/a
39	chr7:99382086-99382136	HMEC	breast:	n/a
40	chr7:99383155-99383205	AoSMC	blood vessel:	n/a
41	chr7:99382086-99382136	IMR90	lung:	fetal
42	chr7:99382370-99382420	BJ	skin:	n/a
43	chr7:99376495-99376545	CMK	blood:	n/a
44	chr7:99383224-99383274	H1-hESC	embryonic stem cell:	embryo
45	chr7:99383224-99383274	NHBE	bronchial:	n/a
46	chr7:99382086-99382136	LNCaP	prostate:	n/a
47	chr7:99382086-99382136	RPTEC	kidney:	n/a
48	chr7:99383224-99383274	NH-A	brain:	n/a
49	chr7:99382370-99382420	Hela-S3	cervix:	n/a
50	chr7:99382086-99382136	GM12878	blood:	n/a

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:99380939..99382491-chr7:99384838..99386622,2	K562	blood:
2	chr7:99355786..99358236-chr7:99360607..99362683,2	K562	blood:
3	chr7:99374500..99377711-chr7:99378798..99381871,3	MCF-7	breast:
4	chr7:99389616..99391219-chr7:99413108..99414812,2	K562	blood:
5	chr7:99389428..99391803-chr7:99419733..99421498,2	MCF-7	breast:
6	chr7:99364077..99366983-chr7:99367660..99369579,3	K562	blood:
7	chr7:99374500..99377711-chr7:99378798..99381871,3	MCF-7	breast:
8	chr7:99358230..99360940-chr7:99460072..99462897,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CYP3A43-6	chr7:99364166-99364515	ENSG00000273407.1

No data

Variant related genes	Relation type
CYP3A4	TF binding region
ENSG00000273407	TF binding region
CYP3A4	CpG island
ENSG00000273407	CpG island
ENSG00000273407	chromatin interactions
ENSG00000160868	chromatin interactions

Extended variants
information (count: 1215 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:1215 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs72552796	chr7:99358521-99358522	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs4986910	chr7:99358524-99358525	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs567089575	chr7:99358537-99358538	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs372741732	chr7:99358541-99358542	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs1041988	chr7:99358566-99358567	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs139109027	chr7:99358581-99358582	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs149870259	chr7:99358596-99358597	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs79432356	chr7:99358607-99358608	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs376135947	chr7:99358614-99358615	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs12721620	chr7:99358615-99358616	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs199747671	chr7:99358632-99358633	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs201416251	chr7:99358633-99358634	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs371799630	chr7:99358649-99358650	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs538621146	chr7:99358655-99358656	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs181454120	chr7:99358662-99358663	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs71582002	chr7:99358672-99358673	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs542714708	chr7:99358682-99358683	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs77669275	chr7:99358693-99358694	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs370999549	chr7:99358702-99358703	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs374415450	chr7:99358798-99358799	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs71582001	chr7:99358800-99358801	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs543655309	chr7:99358803-99358804	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs186138863	chr7:99358823-99358824	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs532734310	chr7:99358877-99358878	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs544276401	chr7:99358946-99358947	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs147712707	chr7:99358989-99358990	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs141108057	chr7:99358994-99358995	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs548237104	chr7:99359007-99359008	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs569818309	chr7:99359012-99359013	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs531531216	chr7:99359044-99359045	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs375064940	chr7:99359049-99359050	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs191940804	chr7:99359058-99359059	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs571505142	chr7:99359069-99359070	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs184241128	chr7:99359084-99359085	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs28988596	chr7:99359098-99359099	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs187531057	chr7:99359120-99359121	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs191165034	chr7:99359121-99359122	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs28988595	chr7:99359135-99359136	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs28988594	chr7:99359141-99359142	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs182271636	chr7:99359149-99359150	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs6956344	chr7:99359151-99359152	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs558919375	chr7:99359207-99359208	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs186836342	chr7:99359208-99359209	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs2687125	chr7:99359227-99359228	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs28988593	chr7:99359243-99359244	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs559630438	chr7:99359261-99359262	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs574445727	chr7:99359267-99359268	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs541869263	chr7:99359271-99359272	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs563434875	chr7:99359419-99359420	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs34382314	chr7:99359483-99359484	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:93)

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
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
Neurodevelopmental disorder	22521361	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Metanephric adenoma	20802469	CNVD
Prostate cancer	16461572	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Malignant melanoma	17260012	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21785460	CNVD
Chronic myeloid leukemia	21384125	CNVD
Bladder cancer	21909424	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Biliary cancer	19435499	CNVD
Myelofibrosis	22110671	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	16608533	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Liver carcinoma	19366792	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Adenocarcinoma	19607727	CNVD
Multiple myeloma	16461302	CNVD
Breast cancer	21858162	CNVD
Emphysema	19352772	CNVD
Effusion lymphoma	18079361	CNVD
Medulloblastoma	17653508	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Autism	19401682	CNVD
Neuroticism	17667963	CNVD
Breast cancer	21509527	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Prostate cancer	18632612	CNVD
Urothelial carcinoma	21177765	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD

Chromatin state (count:250 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:99350800-99359800	Weak transcription	Fetal Lung	lung
2	chr7:99350800-99369800	Weak transcription	Pancreas	Pancrea
3	chr7:99351000-99364000	Weak transcription	Duodenum Mucosa	Duodenum
4	chr7:99355400-99365800	Strong transcription	Liver	Liver
5	chr7:99358200-99359800	Weak transcription	K562	blood
6	chr7:99358400-99360400	Weak transcription	Fetal Intestine Small	intestine
7	chr7:99359600-99360200	Active TSS	Sigmoid Colon	Sigmoid Colon
8	chr7:99359600-99361600	Enhancers	Breast Myoepithelial Primary Cells	Breast
9	chr7:99359600-99361600	Enhancers	Skeletal Muscle Female	skeletal muscle
10	chr7:99359600-99362000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
11	chr7:99359800-99360400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr7:99359800-99360400	Enhancers	K562	blood
13	chr7:99359800-99360600	Enhancers	Fetal Lung	lung
14	chr7:99359800-99361400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr7:99359800-99361400	Enhancers	HMEC	breast
16	chr7:99360000-99360400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
17	chr7:99360000-99360600	Enhancers	NHEK	skin
18	chr7:99360000-99361000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
19	chr7:99360000-99361600	Enhancers	Muscle Satellite Cultured Cells	--
20	chr7:99360000-99361600	Enhancers	Skeletal Muscle Male	skeletal muscle
21	chr7:99360200-99360400	Enhancers	Hela-S3	cervix
22	chr7:99360400-99360600	Enhancers	Fetal Intestine Small	intestine
23	chr7:99360400-99360800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr7:99360400-99360800	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
25	chr7:99360400-99360800	Enhancers	Fetal Muscle Leg	muscle
26	chr7:99360400-99360800	Enhancers	Placenta Amnion	Placenta Amnion
27	chr7:99360400-99360800	Flanking Active TSS	Hela-S3	cervix
28	chr7:99360400-99361000	Enhancers	HSMMtube	muscle
29	chr7:99360400-99361000	Flanking Active TSS	K562	blood
30	chr7:99360400-99361000	Enhancers	Osteobl	bone
31	chr7:99360400-99361200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr7:99360400-99361200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
33	chr7:99360400-99361400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
34	chr7:99360400-99361400	Enhancers	HSMM	muscle
35	chr7:99360400-99361400	Enhancers	NH-A	brain
36	chr7:99360400-99361600	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
37	chr7:99360400-99361600	Enhancers	Stomach Mucosa	stomach
38	chr7:99360600-99360800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
39	chr7:99360600-99360800	Flanking Active TSS	Fetal Lung	lung
40	chr7:99360600-99361000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
41	chr7:99360600-99361000	Flanking Active TSS	NHEK	skin
42	chr7:99360800-99361000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
43	chr7:99360800-99361000	Enhancers	Fetal Lung	lung
44	chr7:99360800-99361400	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr7:99360800-99361400	Active TSS	Fetal Brain Male	brain
46	chr7:99360800-99361400	Enhancers	Hela-S3	cervix
47	chr7:99361000-99361200	Flanking Active TSS	Fetal Lung	lung
48	chr7:99361000-99361200	Enhancers	NHEK	skin
49	chr7:99361000-99361400	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
50	chr7:99361000-99361400	Flanking Active TSS	Osteobl	bone

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