Variant report

Variant	nsv533533
Chromosome Location	chr7:3167411-3214077
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:577)
CpG islands
(count:366)
Chromatin interactive
region (count:22)
LncRNA
region (count:12)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:577 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:3203948-3204296	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:3186430-3186815	K562	blood:	n/a	n/a
3	ATF1	chr7:3174282-3174626	K562	blood:	n/a	n/a
4	BACH1	chr7:3186439-3186846	K562	blood:	n/a	n/a
5	BACH1	chr7:3186456-3186829	H1-hESC	embryonic stem cell:	n/a	n/a
6	BATF	chr7:3192746-3193040	GM12878	blood:	n/a	chr7:3192912-3192923
7	BCL11A	chr7:3192760-3193070	GM12878	blood:	n/a	chr7:3192915-3192924 chr7:3192916-3192925
8	BCL11A	chr7:3192749-3193044	GM12878	blood:	n/a	chr7:3192915-3192924 chr7:3192916-3192925
9	BCLAF1	chr7:3194415-3194858	GM12878	blood:	n/a	n/a
10	BHLHE40	chr7:3168549-3168710	K562	blood:	n/a	chr7:3168685-3168694 chr7:3168679-3168700 chr7:3168683-3168696 chr7:3168686-3168695 chr7:3168685-3168694
11	BHLHE40	chr7:3186430-3186949	K562	blood:	n/a	n/a
12	BRCA1	chr7:3191484-3191701	GM12878	blood:	n/a	n/a
13	CCNT2	chr7:3186464-3186878	K562	blood:	n/a	chr7:3186464-3186473
14	CEBPB	chr7:3186370-3186914	A549	lung:	n/a	n/a
15	CEBPB	chr7:3178482-3178985	K562	blood:	n/a	n/a
16	CEBPB	chr7:3168207-3168382	HepG2	liver:	n/a	chr7:3168316-3168327
17	CEBPB	chr7:3174341-3174612	K562	blood:	n/a	n/a
18	CEBPB	chr7:3186407-3186786	K562	blood:	n/a	n/a
19	CEBPB	chr7:3186997-3187012	K562	blood:	n/a	n/a
20	CEBPB	chr7:3168058-3168534	MCF-7	breast:	n/a	chr7:3168316-3168327
21	CHD2	chr7:3188625-3188930	K562	blood:	n/a	n/a
22	CHD2	chr7:3170188-3170489	K562	blood:	n/a	n/a
23	CHD2	chr7:3191510-3191704	K562	blood:	n/a	n/a
24	CHD2	chr7:3191548-3191696	GM12878	blood:	n/a	n/a
25	CTCF	chr7:3194660-3194810	HAc	cerebellar:	n/a	n/a
26	CTCF	chr7:3194470-3194860	HUVEC	blood vessel:	n/a	n/a
27	CTCF	chr7:3194660-3194810	AG04449	skin:	n/a	n/a
28	CTCF	chr7:3194620-3194770	HMEC	breast:	n/a	n/a
29	CTCF	chr7:3194640-3194790	GM12869	blood:	n/a	n/a
30	CTCF	chr7:3194614-3194825	Pancreas_OC	pancreas:	n/a	n/a
31	CTCF	chr7:3202087-3202105	GM19239	blood:	n/a	n/a
32	CTCF	chr7:3194600-3194750	NHDF-neo	bronchial:	n/a	n/a
33	CTCF	chr7:3194660-3194810	HepG2	liver:	n/a	n/a
34	CTCF	chr7:3194620-3194770	HVMF	connective:	n/a	n/a
35	CTCF	chr7:3202020-3202170	HBMEC	blood vessel:	n/a	chr7:3202038-3202045
36	CTCF	chr7:3194089-3195197	SK-N-SH	brain:	n/a	n/a
37	CTCF	chr7:3194652-3194765	MCF-7	breast:	n/a	n/a
38	CTCF	chr7:3194660-3194810	AG09319	gingival:	n/a	n/a
39	CTCF	chr7:3201980-3202130	HFF-Myc	foreskin:	n/a	chr7:3202038-3202045
40	CTCF	chr7:3194562-3194864	Spleen_OC	spleen:	n/a	n/a
41	CTCF	chr7:3194620-3194770	WI-38	lung:	n/a	n/a
42	CTCF	chr7:3194552-3194562	LNCaP	prostate:	n/a	n/a
43	CTCF	chr7:3194640-3194790	BJ	skin:	n/a	n/a
44	CTCF	chr7:3202160-3202310	HFF-Myc	foreskin:	n/a	n/a
45	CTCF	chr7:3202020-3202170	AG04449	skin:	n/a	chr7:3202038-3202045
46	CTCF	chr7:3185765-3185858	K562	blood:	n/a	n/a
47	CTCF	chr7:3194620-3194770	HRE	kidney:	n/a	n/a
48	CTCF	chr7:3194620-3194770	SAEC	small airway:	n/a	n/a
49	CTCF	chr7:3194996-3195103	Kidney_OC	kidney:	n/a	n/a
50	CTCF	chr7:3194660-3194810	HCM	heart:	n/a	n/a

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:3175091-3175141	Jurkat	blood:	n/a
2	chr7:3186788-3186838	ovcar-3	ovarian:	n/a
3	chr7:3186788-3186838	HRPEpiC	eye:	n/a
4	chr7:3186766-3186816	NH-A	brain:	n/a
5	chr7:3208493-3208543	Jurkat	blood:	n/a
6	chr7:3208493-3208543	HRE	kidney:	n/a
7	chr7:3207719-3207769	PANC-1	pancreas:	n/a
8	chr7:3186766-3186816	PANC-1	pancreas:	n/a
9	chr7:3208493-3208543	K562	blood:	n/a
10	chr7:3186766-3186816	AoSMC	blood vessel:	n/a
11	chr7:3186766-3186816	GM06990	blood:	n/a
12	chr7:3175091-3175141	AG09319	gingival:	n/a
13	chr7:3186788-3186838	NHDF-neo	bronchial:	n/a
14	chr7:3175091-3175141	HEEpiC	esophagus:	n/a
15	chr7:3175091-3175141	Hepatocyte	liver:	n/a
16	chr7:3186766-3186816	HepG2	liver:	n/a
17	chr7:3208793-3208843	LNCaP	prostate:	n/a
18	chr7:3208493-3208543	PANC-1	pancreas:	n/a
19	chr7:3208493-3208543	ProgFib	skin:	n/a
20	chr7:3207719-3207769	Caco-2	colon:	n/a
21	chr7:3186788-3186838	MCF10A-Er-Src	breast:	n/a
22	chr7:3175091-3175141	T-47D	breast:	n/a
23	chr7:3175091-3175141	LNCaP	prostate:	n/a
24	chr7:3186788-3186838	CMK	blood:	n/a
25	chr7:3208493-3208543	HRCEpiC	kidney:	n/a
26	chr7:3186788-3186838	HUVEC	blood vessel:	n/a
27	chr7:3186788-3186838	HCM	heart:	n/a
28	chr7:3186766-3186816	HCT-116	colon:	n/a
29	chr7:3186766-3186816	HEK293	kidney:	embryo
30	chr7:3207719-3207769	ProgFib	skin:	n/a
31	chr7:3208793-3208843	HCT-116	colon:	n/a
32	chr7:3207719-3207769	LNCaP	prostate:	n/a
33	chr7:3186766-3186816	HUVEC	blood vessel:	n/a
34	chr7:3175091-3175141	HIPEpiC	eye:	n/a
35	chr7:3186766-3186816	NB4	blood:	n/a
36	chr7:3186788-3186838	SAEC	small airway:	n/a
37	chr7:3175091-3175141	HepG2	liver:	n/a
38	chr7:3208793-3208843	MCF10A-Er-Src	breast:	n/a
39	chr7:3186788-3186838	NHBE	bronchial:	n/a
40	chr7:3207719-3207769	NH-A	brain:	n/a
41	chr7:3208793-3208843	T-47D	breast:	n/a
42	chr7:3186788-3186838	ECC-1	luminal epithelium:	n/a
43	chr7:3208793-3208843	PrEC	prostate:	n/a
44	chr7:3186788-3186838	SK-N-MC	brain:	n/a
45	chr7:3208493-3208543	HCPEpiC	choroid plexus:	n/a
46	chr7:3207719-3207769	U87	brain:	n/a
47	chr7:3175091-3175141	SK-N-SH_RA	brain:	n/a
48	chr7:3207719-3207769	GM06990	blood:	n/a
49	chr7:3186766-3186816	GM19239	blood:	n/a
50	chr7:3175091-3175141	HCT-116	colon:	n/a

(count:22 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:3210617..3212945-chr7:3214732..3216839,2	K562	blood:
2	chr7:3194510..3195232-chr7:3340158..3340723,2	MCF-7	breast:
3	chr7:3201417..3202351-chr7:3240242..3240878,3	MCF-7	breast:
4	chr7:3205607..3207977-chr7:3220687..3223407,2	K562	blood:
5	chr7:3184853..3186673-chr7:3189363..3191376,2	K562	blood:
6	chr7:3184853..3186673-chr7:3189363..3191376,2	K562	blood:
7	chr7:3104949..3105997-chr7:3194351..3195035,3	MCF-7	breast:
8	chr7:3194262..3194922-chr7:3439333..3439841,2	MCF-7	breast:
9	chr7:2904357..2905298-chr7:3194209..3195076,4	K562	blood:
10	chr7:3105018..3105890-chr7:3193882..3195188,3	MCF-7	breast:
11	chr7:2710484..2711053-chr7:3194317..3194955,2	K562	blood:
12	chr7:3172781..3176010-chr7:3179517..3182340,3	K562	blood:
13	chr7:2926262..2927534-chr7:3194238..3195613,6	MCF-7	breast:
14	chr7:3172781..3176010-chr7:3179517..3182340,3	K562	blood:
15	chr7:3105046..3105933-chr7:3194248..3194999,3	K562	blood:
16	chr7:3198032..3200716-chr7:3210631..3213455,2	MCF-7	breast:
17	chr7:2913057..2915172-chr7:3198284..3201204,2	MCF-7	breast:
18	chr7:3210553..3212945-chr7:3214110..3216839,3	K562	blood:
19	chr7:3210592..3212478-chr7:3220599..3222530,2	K562	blood:
20	chr7:2914055..2915867-chr7:3204506..3206043,2	MCF-7	breast:
21	chr7:2925307..2926930-chr7:3193219..3196331,3	MCF-7	breast:
22	chr11:108535309..108536048-chr7:3168253..3168776,2	HCT-116	colon:

(count:12 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CARD11-4	chr7:3204171-3204221	NONHSAT118845
2	lnc-AC091801.1.1-1	chr7:3186629-3186905	XLOC_006339
3	lnc-AC091801.1.1-8	chr7:3172190-3172290	ucscGeneNc_uc003smw_1
4	lnc-CARD11-4	chr7:3202784-3203088	NONHSAT118845
5	lnc-AC091801.1.1-1	chr7:3197771-3197975	XLOC_006339
6	lnc-AC091801.1.1-1	chr7:3205664-3205764	XLOC_006339
7	lnc-AC091801.1.1-1	chr7:3197771-3197888	XLOC_006339
8	lnc-CARD11-4	chr7:3204353-3204414	NONHSAT118845
9	lnc-AC091801.1.1-1	chr7:3179828-3179930	XLOC_006339
10	lnc-AC091801.1.1-1	chr7:3186629-3186905	NONHSAT118844
11	lnc-AC091801.1.1-8	chr7:3180756-3180813	ucscGeneNc_uc003smw_1
12	lnc-AC091801.1.1-1	chr7:3205664-3205764	NONHSAT118844

No data

Variant related genes	Relation type
ENSG00000217455	TF binding region
ENSG00000217455	CpG island
ENSG00000217455	chromatin interactions
ENSG00000178105	chromatin interactions

Extended variants
information (count: 2726 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:2726 , 50 per page) page: 1 2 3 4 5 6 7 ... 55

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs541845495	chr7:3167800-3167801	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs142490951	chr7:3167832-3167833	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs370410192	chr7:3167835-3167836	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs146762869	chr7:3167865-3167866	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs544032642	chr7:3167884-3167885	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs563948957	chr7:3167887-3167888	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs138765487	chr7:3167907-3167908	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs545891474	chr7:3167914-3167915	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs149267383	chr7:3167918-3167919	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs191474723	chr7:3167922-3167923	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs183737206	chr7:3167924-3167925	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs377081485	chr7:3167925-3167926	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs75116780	chr7:3167938-3167939	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs143462125	chr7:3167941-3167942	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs541677759	chr7:3167946-3167947	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs531242314	chr7:3168025-3168026	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs147974475	chr7:3168026-3168027	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs141796443	chr7:3168028-3168029	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs186002840	chr7:3168037-3168038	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs568727667	chr7:3168057-3168058	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs571806865	chr7:3168087-3168088	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs546705320	chr7:3168091-3168092	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs150578821	chr7:3168096-3168097	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs386709426	chr7:3168102-3168103	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs182710322	chr7:3168103-3168104	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs368202841	chr7:3168111-3168112	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs537739238	chr7:3168125-3168126	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs75241698	chr7:3168136-3168137	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs116563430	chr7:3168152-3168153	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs75563645	chr7:3168160-3168161	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs186627747	chr7:3168164-3168165	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs138756166	chr7:3168184-3168185	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs554555960	chr7:3168208-3168209	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs191074472	chr7:3168238-3168239	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs541817805	chr7:3168242-3168243	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs562101121	chr7:3168251-3168252	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs530854371	chr7:3168262-3168263	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs372841101	chr7:3168270-3168271	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs77310095	chr7:3168272-3168273	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs78090354	chr7:3168273-3168274	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs564803442	chr7:3168274-3168275	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs146237569	chr7:3168289-3168290	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs183642533	chr7:3168297-3168298	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs140092175	chr7:3168299-3168300	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs117777926	chr7:3168300-3168301	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs189131800	chr7:3168313-3168314	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs568832530	chr7:3168329-3168330	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs79854224	chr7:3168353-3168354	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs149790881	chr7:3168364-3168365	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs375527655	chr7:3168381-3168382	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:80)

Disease	PMID	Source
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Chordoma	21602918	CNVD
Lynch syndrome	22585707	CNVD
Follicular lymphoma	20505157	CNVD
Breast cancer	16397240	CNVD
Raine Syndrome	17924334	CNVD
Diffuse large b-cell lymphoma	21266526	CNVD
Melanoma	18172304	CNVD
Sudden cardiac death	19188705	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Glioma	18556773	CNVD
Ovarian cancer	21720365	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Ovarian cancer	22174824	CNVD
Urothelial carcinoma	18382360	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Biliary cancer	19435499	CNVD
Cancer	16751803	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	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
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Developmental delay	21147756	CNVD
Prostate cancer	18632612	CNVD
Urothelial carcinoma	21177765	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Nasopharyngeal cancer	20548289	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
Spondylocostal dysostosis	21085971	CNVD
Mental retardation	17901693	CNVD
Heart disease	21282601	CNVD
Glioblastoma multiforme	22286061	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	17053054	CNVD
Cancer	20164920	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:243 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:3167800-3168800	Enhancers	Breast Myoepithelial Primary Cells	Breast
2	chr7:3168200-3168600	Enhancers	Primary hematopoietic stem cells short term culture	blood
3	chr7:3168600-3169000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
4	chr7:3168600-3169800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr7:3169000-3169600	Enhancers	Primary hematopoietic stem cells short term culture	blood
6	chr7:3169800-3189400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr7:3172800-3173000	Enhancers	Primary hematopoietic stem cells	blood
8	chr7:3172800-3175600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr7:3173000-3174000	Weak transcription	Primary hematopoietic stem cells	blood
10	chr7:3173000-3174800	Enhancers	Primary hematopoietic stem cells short term culture	blood
11	chr7:3173200-3174800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr7:3174000-3174800	Enhancers	Primary hematopoietic stem cells	blood
13	chr7:3174400-3175000	Enhancers	HUES48 Cell Line	embryonic stem cell
14	chr7:3174400-3175200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
15	chr7:3174400-3175600	Enhancers	HUES64 Cell Line	embryonic stem cell
16	chr7:3174400-3176200	Enhancers	iPS-18 Cell Line	embryonic stem cell
17	chr7:3174600-3175600	Enhancers	HUES6 Cell Line	embryonic stem cell
18	chr7:3174600-3176000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr7:3174600-3176400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr7:3174800-3175200	Enhancers	H9 Cell Line	embryonic stem cell
21	chr7:3174800-3175200	Enhancers	iPS-15b Cell Line	embryonic stem cell
22	chr7:3174800-3175400	Enhancers	H1 Cell Line	embryonic stem cell
23	chr7:3174800-3175800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
24	chr7:3174800-3175800	Enhancers	Cortex derived primary cultured neurospheres	brain
25	chr7:3174800-3178600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
26	chr7:3175000-3175200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
27	chr7:3175000-3175400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
28	chr7:3175000-3175600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr7:3175000-3178400	Weak transcription	HUES48 Cell Line	embryonic stem cell
30	chr7:3175200-3175800	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
31	chr7:3175400-3178400	Weak transcription	H1 Cell Line	embryonic stem cell
32	chr7:3175600-3178400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr7:3175800-3176000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
34	chr7:3175800-3178600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
35	chr7:3178400-3178800	Enhancers	HUES48 Cell Line	embryonic stem cell
36	chr7:3178400-3179000	Enhancers	H1 Cell Line	embryonic stem cell
37	chr7:3178400-3179000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr7:3178400-3204600	Weak transcription	Right Atrium	heart
39	chr7:3178600-3178800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
40	chr7:3178600-3179200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
41	chr7:3178800-3179200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
42	chr7:3179200-3179600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
43	chr7:3179400-3179800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
44	chr7:3179400-3180000	Enhancers	Brain Germinal Matrix	brain
45	chr7:3180000-3180600	Enhancers	Fetal Brain Male	brain
46	chr7:3180000-3183200	Weak transcription	Brain Germinal Matrix	brain
47	chr7:3180200-3180800	Enhancers	Fetal Stomach	stomach
48	chr7:3180600-3183200	Weak transcription	Fetal Brain Male	brain
49	chr7:3180800-3183600	Weak transcription	Fetal Stomach	stomach
50	chr7:3183200-3184200	Enhancers	Fetal Brain Male	brain

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