Variant report

Variant	nsv482109
Chromosome Location	chr7:99354604-99381808
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:174)
CpG islands
(count:122)
Chromatin interactive
region (count:7)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:174 , 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	chr7:99365247-99365623	GM12878	blood:	n/a	n/a
6	BATF	chr7:99365239-99365549	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	chr7:99365355-99365633	GM12878	blood:	n/a	n/a
10	BHLHE40	chr7:99360674-99360886	K562	blood:	n/a	n/a
11	CBX3	chr7:99360292-99360970	K562	blood:	n/a	n/a
12	CEBPB	chr7:99370271-99370552	HepG2	liver:	n/a	n/a
13	CEBPB	chr7:99354505-99354705	IMR90	lung:	n/a	chr7:99354587-99354598 chr7:99354587-99354600 chr7:99354589-99354600
14	CEBPB	chr7:99354474-99354734	K562	blood:	n/a	chr7:99354587-99354598 chr7:99354587-99354600 chr7:99354589-99354600
15	CEBPB	chr7:99354480-99354737	A549	lung:	n/a	chr7:99354587-99354598 chr7:99354587-99354600 chr7:99354589-99354600
16	CEBPB	chr7:99370297-99370473	HepG2	liver:	n/a	n/a
17	CEBPB	chr7:99360356-99360612	K562	blood:	n/a	n/a
18	CEBPB	chr7:99354445-99354721	HepG2	liver:	n/a	chr7:99354587-99354598 chr7:99354587-99354600 chr7:99354589-99354600
19	CHD2	chr7:99365347-99365565	GM12878	blood:	n/a	n/a
20	CTCF	chr7:99379960-99380110	HEK293	kidney:	n/a	n/a
21	CTCF	chr7:99379940-99380090	HMEC	breast:	n/a	n/a
22	CTCF	chr7:99379900-99380050	GM12872	blood:	n/a	n/a
23	CTCF	chr7:99379946-99380130	K562	blood:	n/a	n/a
24	CTCF	chr7:99379520-99379670	GM12869	blood:	n/a	n/a
25	CTCF	chr7:99379926-99380103	HepG2	liver:	n/a	n/a
26	CTCF	chr7:99379904-99380157	K562	blood:	n/a	n/a
27	CTCF	chr7:99379920-99380070	RPTEC	kidney:	n/a	n/a
28	CTCF	chr7:99380003-99380091	HepG2	liver:	n/a	n/a
29	CTCF	chr7:99380023-99380072	Hela-S3	cervix:	n/a	n/a
30	CTCF	chr7:99379980-99380130	MCF-7	breast:	n/a	n/a
31	CTCF	chr7:99379940-99380090	HepG2	liver:	n/a	n/a
32	CTCF	chr7:99379980-99380130	K562	blood:	n/a	n/a
33	CUX1	chr7:99365256-99365588	GM12878	blood:	n/a	n/a
34	CUX1	chr7:99358092-99358259	K562	blood:	n/a	n/a
35	CUX1	chr7:99360597-99361175	K562	blood:	n/a	n/a
36	EBF1	chr7:99365230-99365634	GM12878	blood:	n/a	chr7:99365456-99365467
37	EBF1	chr7:99360832-99361020	GM12878	blood:	n/a	n/a
38	EBF1	chr7:99365268-99365651	GM12878	blood:	n/a	chr7:99365456-99365467
39	EBF1	chr7:99365165-99365749	GM12878	blood:	n/a	chr7:99365456-99365467
40	EBF1	chr7:99361696-99361858	GM12878	blood:	n/a	n/a
41	ELF1	chr7:99370237-99370540	HepG2	liver:	n/a	n/a
42	ELK1	chr7:99365390-99365532	GM12878	blood:	n/a	n/a
43	EP300	chr7:99370150-99370588	HepG2	liver:	n/a	chr7:99370459-99370466
44	EP300	chr7:99365314-99365626	GM12878	blood:	n/a	n/a
45	EP300	chr7:99365290-99365561	GM12878	blood:	n/a	n/a
46	EP300	chr7:99360387-99360956	K562	blood:	n/a	n/a
47	EP300	chr7:99364259-99364654	Hela-S3	cervix:	n/a	n/a
48	EP300	chr7:99370182-99370601	HepG2	liver:	n/a	chr7:99370459-99370466
49	FOS	chr7:99360591-99360934	MCF10A-Er-Src	breast:	n/a	chr7:99360745-99360755
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:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:99355204-99355254	RPTEC	kidney:	n/a
2	chr7:99355204-99355254	HCM	heart:	n/a
3	chr7:99376495-99376545	SK-N-SH	brain:	n/a
4	chr7:99376495-99376545	K562	blood:	n/a
5	chr7:99376495-99376545	NT2-D1	testis:	n/a
6	chr7:99376495-99376545	ovcar-3	ovarian:	n/a
7	chr7:99355204-99355254	PrEC	prostate:	n/a
8	chr7:99355204-99355254	HEEpiC	esophagus:	n/a
9	chr7:99355204-99355254	ECC-1	luminal epithelium:	n/a
10	chr7:99376495-99376545	AoSMC	blood vessel:	n/a
11	chr7:99376495-99376545	BE2_C	brain:	n/a
12	chr7:99376495-99376545	ProgFib	skin:	n/a
13	chr7:99355204-99355254	HAEpiC	amniotic membrane:	n/a
14	chr7:99376495-99376545	AG09309	skin:	n/a
15	chr7:99376495-99376545	NHBE	bronchial:	n/a
16	chr7:99355204-99355254	Hepatocyte	liver:	n/a
17	chr7:99376495-99376545	GM12892	blood:	n/a
18	chr7:99376495-99376545	GM12878	blood:	n/a
19	chr7:99355204-99355254	U87	brain:	n/a
20	chr7:99376495-99376545	HRPEpiC	eye:	n/a
21	chr7:99376495-99376545	PFSK-1	brain:	n/a
22	chr7:99376495-99376545	ECC-1	luminal epithelium:	n/a
23	chr7:99376495-99376545	AG04450	lung:	fetal
24	chr7:99376495-99376545	H1-hESC	embryonic stem cell:	embryo
25	chr7:99376495-99376545	BJ	skin:	n/a
26	chr7:99355204-99355254	IMR90	lung:	fetal
27	chr7:99355204-99355254	Caco-2	colon:	n/a
28	chr7:99355204-99355254	HRE	kidney:	n/a
29	chr7:99355204-99355254	AG09309	skin:	n/a
30	chr7:99376495-99376545	SK-N-MC	brain:	n/a
31	chr7:99355204-99355254	PFSK-1	brain:	n/a
32	chr7:99355204-99355254	HepG2	liver:	n/a
33	chr7:99376495-99376545	CMK	blood:	n/a
34	chr7:99355204-99355254	HL-60	blood:	n/a
35	chr7:99376495-99376545	MCF-7	breast:	n/a
36	chr7:99376495-99376545	LNCaP	prostate:	n/a
37	chr7:99355204-99355254	NB4	blood:	n/a
38	chr7:99376495-99376545	HCPEpiC	choroid plexus:	n/a
39	chr7:99355204-99355254	AoSMC	blood vessel:	n/a
40	chr7:99376495-99376545	HAEpiC	amniotic membrane:	n/a
41	chr7:99376495-99376545	HCF	heart:	n/a
42	chr7:99355204-99355254	GM12878	blood:	n/a
43	chr7:99376495-99376545	MCF10A-Er-Src	breast:	n/a
44	chr7:99355204-99355254	HRCEpiC	kidney:	n/a
45	chr7:99376495-99376545	U87	brain:	n/a
46	chr7:99355204-99355254	SK-N-SH	brain:	n/a
47	chr7:99376495-99376545	SK-N-SH_RA	brain:	n/a
48	chr7:99355204-99355254	BE2_C	brain:	n/a
49	chr7:99355204-99355254	Hela-S3	cervix:	n/a
50	chr7:99376495-99376545	HCM	heart:	n/a

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:99355786..99358236-chr7:99360607..99362683,2	K562	blood:
2	chr7:99374500..99377711-chr7:99378798..99381871,3	MCF-7	breast:
3	chr7:99364077..99366983-chr7:99367660..99369579,3	K562	blood:
4	chr7:99358230..99360940-chr7:99460072..99462897,2	K562	blood:
5	chr7:99374500..99377711-chr7:99378798..99381871,3	MCF-7	breast:
6	chr7:99355786..99358236-chr7:99360607..99362683,2	K562	blood:
7	chr7:99348892..99351554-chr7:99353145..99355344,2	MCF-7	breast:

(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

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	CYP3A4	hsa-miR-27b-3p	chr7:99355142-99355162

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: 1057 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:1057 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs185997841	chr7:99354611-99354612	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs575516082	chr7:99354616-99354617	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs367576049	chr7:99354630-99354631	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs558444773	chr7:99354634-99354635	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs28988606	chr7:99354661-99354662	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs562115782	chr7:99354745-99354746	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs28371763	chr7:99354808-99354809	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs534020143	chr7:99354908-99354909	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs34469568	chr7:99354937-99354938	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs117070162	chr7:99354947-99354948	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs28969391	chr7:99354989-99354990	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs33972239	chr7:99354990-99354991	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs371661164	chr7:99355038-99355039	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs369197496	chr7:99355072-99355073	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs28988604	chr7:99355073-99355074	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs34554553	chr7:99355093-99355094	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs368818197	chr7:99355098-99355099	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs28371762	chr7:99355166-99355167	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs528029485	chr7:99355172-99355173	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs28988603	chr7:99355185-99355186	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs12721626	chr7:99355278-99355279	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs528988199	chr7:99355293-99355294	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs550740702	chr7:99355341-99355342	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs569081546	chr7:99355355-99355356	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs190760449	chr7:99355365-99355366	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs558124508	chr7:99355367-99355368	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs183096525	chr7:99355426-99355427	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs12721631	chr7:99355427-99355428	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs59715127	chr7:99355490-99355491	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs147937926	chr7:99355508-99355509	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs2740581	chr7:99355519-99355520	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs12721621	chr7:99355612-99355613	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs79723636	chr7:99355626-99355627	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs35494189	chr7:99355629-99355630	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs71581999	chr7:99355649-99355650	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs34141638	chr7:99355660-99355661	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs72552794	chr7:99355683-99355684	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs370438919	chr7:99355710-99355711	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs575306131	chr7:99355718-99355719	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs371455509	chr7:99355726-99355727	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs192313684	chr7:99355729-99355730	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs372534674	chr7:99355738-99355739	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs147125009	chr7:99355771-99355772	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs148317879	chr7:99355789-99355790	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs138550343	chr7:99355803-99355804	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs67666821	chr7:99355806-99355807	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs374814627	chr7:99355827-99355828	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs60535349	chr7:99355836-99355837	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs28371761	chr7:99355843-99355844	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs141749477	chr7:99355852-99355853	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:94)

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
Cancer	20164919	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD

Chromatin state (count:151 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:99350000-99355400	Weak transcription	Liver	Liver
2	chr7:99350800-99357600	Weak transcription	Fetal Intestine Small	intestine
3	chr7:99350800-99359800	Weak transcription	Fetal Lung	lung
4	chr7:99350800-99369800	Weak transcription	Pancreas	Pancrea
5	chr7:99351000-99364000	Weak transcription	Duodenum Mucosa	Duodenum
6	chr7:99352800-99355600	Weak transcription	Aorta	Aorta
7	chr7:99355400-99365800	Strong transcription	Liver	Liver
8	chr7:99357400-99358400	Enhancers	HepG2	liver
9	chr7:99357600-99358400	Enhancers	Fetal Intestine Small	intestine
10	chr7:99357800-99358200	Enhancers	Fetal Intestine Large	intestine
11	chr7:99358000-99358200	Enhancers	K562	blood
12	chr7:99358200-99359800	Weak transcription	K562	blood
13	chr7:99358400-99360400	Weak transcription	Fetal Intestine Small	intestine
14	chr7:99359600-99360200	Active TSS	Sigmoid Colon	Sigmoid Colon
15	chr7:99359600-99361600	Enhancers	Breast Myoepithelial Primary Cells	Breast
16	chr7:99359600-99361600	Enhancers	Skeletal Muscle Female	skeletal muscle
17	chr7:99359600-99362000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
18	chr7:99359800-99360400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
19	chr7:99359800-99360400	Enhancers	K562	blood
20	chr7:99359800-99360600	Enhancers	Fetal Lung	lung
21	chr7:99359800-99361400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr7:99359800-99361400	Enhancers	HMEC	breast
23	chr7:99360000-99360400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
24	chr7:99360000-99360600	Enhancers	NHEK	skin
25	chr7:99360000-99361000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
26	chr7:99360000-99361600	Enhancers	Muscle Satellite Cultured Cells	--
27	chr7:99360000-99361600	Enhancers	Skeletal Muscle Male	skeletal muscle
28	chr7:99360200-99360400	Enhancers	Hela-S3	cervix
29	chr7:99360400-99360600	Enhancers	Fetal Intestine Small	intestine
30	chr7:99360400-99360800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr7:99360400-99360800	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
32	chr7:99360400-99360800	Enhancers	Fetal Muscle Leg	muscle
33	chr7:99360400-99360800	Enhancers	Placenta Amnion	Placenta Amnion
34	chr7:99360400-99360800	Flanking Active TSS	Hela-S3	cervix
35	chr7:99360400-99361000	Enhancers	HSMMtube	muscle
36	chr7:99360400-99361000	Flanking Active TSS	K562	blood
37	chr7:99360400-99361000	Enhancers	Osteobl	bone
38	chr7:99360400-99361200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
39	chr7:99360400-99361200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr7:99360400-99361400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
41	chr7:99360400-99361400	Enhancers	HSMM	muscle
42	chr7:99360400-99361400	Enhancers	NH-A	brain
43	chr7:99360400-99361600	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chr7:99360400-99361600	Enhancers	Stomach Mucosa	stomach
45	chr7:99360600-99360800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
46	chr7:99360600-99360800	Flanking Active TSS	Fetal Lung	lung
47	chr7:99360600-99361000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr7:99360600-99361000	Flanking Active TSS	NHEK	skin
49	chr7:99360800-99361000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
50	chr7:99360800-99361000	Enhancers	Fetal Lung	lung

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