Variant report

Variant	esv3349195
Chromosome Location	chr7:128887559-128918489
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:364)
CpG islands
(count:122)
Chromatin interactive
region (count:32)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:364 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:128911516-128912004	K562	blood:	n/a	n/a
2	ARID3A	chr7:128911652-128911897	HepG2	liver:	n/a	n/a
3	ATF2	chr7:128898617-128899057	H1-hESC	embryonic stem cell:	n/a	n/a
4	BHLHE40	chr7:128905274-128905613	K562	blood:	n/a	n/a
5	BHLHE40	chr7:128892280-128892438	K562	blood:	n/a	n/a
6	BHLHE40	chr7:128911632-128911892	K562	blood:	n/a	n/a
7	BRCA1	chr7:128899013-128899016	H1-hESC	embryonic stem cell:	n/a	n/a
8	CBX3	chr7:128911516-128911939	K562	blood:	n/a	n/a
9	CEBPB	chr7:128899430-128899728	IMR90	lung:	n/a	n/a
10	CEBPB	chr7:128906887-128906987	HepG2	liver:	n/a	chr7:128906961-128906974
11	CEBPZ	chr7:128911696-128911895	HepG2	liver:	n/a	n/a
12	CTCF	chr7:128911756-128911840	GM12891	blood:	n/a	n/a
13	CTCF	chr7:128911720-128911870	HPF	lung:	n/a	n/a
14	CTCF	chr7:128911720-128911870	BJ	skin:	n/a	n/a
15	CTCF	chr7:128911680-128911830	WI-38	lung:	n/a	n/a
16	CTCF	chr7:128911679-128911850	SK-N-SH_RA	brain:	n/a	n/a
17	CTCF	chr7:128911597-128911944	IMR90	lung:	n/a	n/a
18	CTCF	chr7:128911567-128911951	A549	lung:	n/a	n/a
19	CTCF	chr7:128911700-128911850	GM12864	blood:	n/a	n/a
20	CTCF	chr7:128911693-128911887	GM10248	blood:	n/a	n/a
21	CTCF	chr7:128911292-128912184	A549	lung:	n/a	n/a
22	CTCF	chr7:128911740-128911890	GM12871	blood:	n/a	n/a
23	CTCF	chr7:128911603-128911885	HepG2	liver:	n/a	n/a
24	CTCF	chr7:128911680-128911830	HMF	breast:	n/a	n/a
25	CTCF	chr7:128911673-128911901	Fibrobl	skin:	n/a	n/a
26	CTCF	chr7:128911703-128911884	MCF-7	breast:	n/a	n/a
27	CTCF	chr7:128911681-128911880	A549	lung:	n/a	n/a
28	CTCF	chr7:128911700-128911850	GM12866	blood:	n/a	n/a
29	CTCF	chr7:128912080-128912091	ProgFib	skin:	n/a	n/a
30	CTCF	chr7:128911700-128911850	HRE	kidney:	n/a	n/a
31	CTCF	chr7:128911740-128911890	NHEK	skin:	n/a	n/a
32	CTCF	chr7:128911680-128911830	AoAF	blood vessel:	n/a	n/a
33	CTCF	chr7:128911720-128911870	GM12870	blood:	n/a	n/a
34	CTCF	chr7:128911720-128911870	A549	lung:	n/a	n/a
35	CTCF	chr7:128911640-128911790	GM12867	blood:	n/a	n/a
36	CTCF	chr7:128911720-128911870	HFF-Myc	foreskin:	n/a	n/a
37	CTCF	chr7:128911702-128911876	A549	lung:	n/a	n/a
38	CTCF	chr7:128911643-128911985	Gliobla	brain:	n/a	n/a
39	CTCF	chr7:128911700-128911850	HBMEC	blood vessel:	n/a	n/a
40	CTCF	chr7:128911740-128911890	HEK293	kidney:	n/a	n/a
41	CTCF	chr7:128911720-128911870	NHEK	skin:	n/a	n/a
42	CTCF	chr7:128911700-128911850	HMF	breast:	n/a	n/a
43	CTCF	chr7:128911660-128911810	SAEC	small airway:	n/a	n/a
44	CTCF	chr7:128911680-128911830	Caco-2	colon:	n/a	n/a
45	CTCF	chr7:128911780-128911930	HAc	cerebellar:	n/a	n/a
46	CTCF	chr7:128911700-128911850	HCPEpiC	choroid plexus:	n/a	n/a
47	CTCF	chr7:128911541-128912086	K562	blood:	n/a	n/a
48	CTCF	chr7:128911701-128911866	MCF-7	breast:	n/a	n/a
49	CTCF	chr7:128911700-128911850	AoAF	blood vessel:	n/a	n/a
50	CTCF	chr7:128911695-128911872	GM19239	blood:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:128905727-128905777	CMK	blood:	n/a
2	chr7:128899554-128899604	HCPEpiC	choroid plexus:	n/a
3	chr7:128899554-128899604	BJ	skin:	n/a
4	chr7:128899554-128899604	BE2_C	brain:	n/a
5	chr7:128899554-128899604	HL-60	blood:	n/a
6	chr7:128899554-128899604	NHBE	bronchial:	n/a
7	chr7:128905727-128905777	U87	brain:	n/a
8	chr7:128899554-128899604	HIPEpiC	eye:	n/a
9	chr7:128899554-128899604	MCF10A-Er-Src	breast:	n/a
10	chr7:128905727-128905777	NH-A	brain:	n/a
11	chr7:128899554-128899604	HNPCEpiC	eye:	n/a
12	chr7:128905727-128905777	GM12892	blood:	n/a
13	chr7:128905727-128905777	Caco-2	colon:	n/a
14	chr7:128905727-128905777	HepG2	liver:	n/a
15	chr7:128905727-128905777	PrEC	prostate:	n/a
16	chr7:128899554-128899604	A549	lung:	n/a
17	chr7:128905727-128905777	A549	lung:	n/a
18	chr7:128905727-128905777	IMR90	lung:	fetal
19	chr7:128905727-128905777	HL-60	blood:	n/a
20	chr7:128905727-128905777	AG09319	gingival:	n/a
21	chr7:128905727-128905777	BJ	skin:	n/a
22	chr7:128905727-128905777	PANC-1	pancreas:	n/a
23	chr7:128899554-128899604	K562	blood:	n/a
24	chr7:128899554-128899604	NB4	blood:	n/a
25	chr7:128905727-128905777	HRPEpiC	eye:	n/a
26	chr7:128899554-128899604	HRE	kidney:	n/a
27	chr7:128899554-128899604	HepG2	liver:	n/a
28	chr7:128905727-128905777	ProgFib	skin:	n/a
29	chr7:128899554-128899604	NT2-D1	testis:	n/a
30	chr7:128905727-128905777	T-47D	breast:	n/a
31	chr7:128905727-128905777	SK-N-SH	brain:	n/a
32	chr7:128899554-128899604	NHDF-neo	bronchial:	n/a
33	chr7:128905727-128905777	HCF	heart:	n/a
34	chr7:128905727-128905777	MCF10A-Er-Src	breast:	n/a
35	chr7:128899554-128899604	AG04450	lung:	fetal
36	chr7:128899554-128899604	SAEC	small airway:	n/a
37	chr7:128899554-128899604	T-47D	breast:	n/a
38	chr7:128905727-128905777	HEEpiC	esophagus:	n/a
39	chr7:128905727-128905777	HCM	heart:	n/a
40	chr7:128905727-128905777	AoSMC	blood vessel:	n/a
41	chr7:128899554-128899604	RPTEC	kidney:	n/a
42	chr7:128905727-128905777	HRE	kidney:	n/a
43	chr7:128899554-128899604	HEEpiC	esophagus:	n/a
44	chr7:128899554-128899604	GM12878	blood:	n/a
45	chr7:128899554-128899604	AoSMC	blood vessel:	n/a
46	chr7:128899554-128899604	PANC-1	pancreas:	n/a
47	chr7:128905727-128905777	HMEC	breast:	n/a
48	chr7:128899554-128899604	GM12892	blood:	n/a
49	chr7:128899554-128899604	HCF	heart:	n/a
50	chr7:128899554-128899604	AG10803	skin:	n/a

(count:32 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:128886315..128888707-chr7:128895408..128897456,2	K562	blood:
2	chr7:128907905..128909932-chr7:128912408..128913916,2	K562	blood:
3	chr7:128890270..128893260-chr7:128905133..128906966,2	MCF-7	breast:
4	chr7:128863759..128868024-chr7:128894474..128897636,4	MCF-7	breast:
5	chr7:128911298..128913685-chr7:128916132..128918074,2	K562	blood:
6	chr7:128858132..128859063-chr7:128911285..128912259,10	K562	blood:
7	chr7:128857969..128858990-chr7:128911282..128912153,7	MCF-7	breast:
8	chr7:128904465..128906876-chr7:128909348..128911601,2	K562	blood:
9	chr7:128887131..128889501-chr7:128893750..128895547,2	K562	blood:
10	chr7:128904465..128906876-chr7:128909348..128911601,2	K562	blood:
11	chr7:128895520..128897910-chr7:128898805..128901095,3	K562	blood:
12	chr7:128909835..128912504-chr7:128923384..128925064,2	K562	blood:
13	chr7:128890270..128893260-chr7:128905133..128906966,2	MCF-7	breast:
14	chr7:128891593..128894019-chr7:128897274..128899185,2	K562	blood:
15	chr7:128887131..128889501-chr7:128893750..128895547,2	K562	blood:
16	chr7:128896827..128899208-chr7:128904608..128906454,2	MCF-7	breast:
17	chr7:128891593..128894019-chr7:128897274..128899185,2	K562	blood:
18	chr7:128862039..128864995-chr7:128907880..128909568,3	K562	blood:
19	chr7:128911298..128913685-chr7:128916132..128918074,2	K562	blood:
20	chr7:128858187..128860723-chr7:128902918..128905516,2	K562	blood:
21	chr7:128866260..128868499-chr7:128899979..128902017,2	K562	blood:
22	chr7:128864080..128864690-chr7:128911590..128912236,2	K562	blood:
23	chr7:128894179..128896664-chr7:128896998..128898691,2	MCF-7	breast:
24	chr7:128861593..128863615-chr7:128915544..128917279,2	K562	blood:
25	chr7:128907905..128909932-chr7:128912408..128913916,2	K562	blood:
26	chr7:128863320..128866916-chr7:128907366..128912174,7	MCF-7	breast:
27	chr7:128895520..128897910-chr7:128898805..128901095,3	K562	blood:
28	chr7:128894179..128896664-chr7:128896998..128898691,2	MCF-7	breast:
29	chr7:128858077..128858720-chr7:128911733..128912346,2	MCF-7	breast:
30	chr7:128886315..128888707-chr7:128895408..128897456,2	K562	blood:
31	chr19:1044541..1045041-chr7:128897386..128898290,2	K562	blood:
32	chr7:128896827..128899208-chr7:128904608..128906454,2	MCF-7	breast:

No data

Variant related genes	Relation type
AHCYL2	TF binding region
AHCYL2	CpG island
ENSG00000158467	chromatin interactions

Extended variants
information (count: 1040 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:1040 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs374552108	chr7:128887617-128887618	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs190056546	chr7:128887662-128887663	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs538753817	chr7:128887682-128887683	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs34605112	chr7:128887710-128887711	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs554280822	chr7:128887731-128887732	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs572529889	chr7:128887735-128887736	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs543231581	chr7:128887748-128887749	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs555222229	chr7:128887777-128887778	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs138717393	chr7:128887791-128887792	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs370996524	chr7:128887810-128887811	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs528110024	chr7:128887820-128887821	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs544139348	chr7:128887870-128887871	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs559718973	chr7:128887898-128887899	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs67820265	chr7:128887925-128887926	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs532183349	chr7:128887934-128887935	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs73721598	chr7:128888004-128888005	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs559434418	chr7:128888007-128888008	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs540881974	chr7:128888018-128888019	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs565173142	chr7:128888021-128888022	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs547955443	chr7:128888031-128888032	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs569531040	chr7:128888043-128888044	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs116188932	chr7:128888106-128888107	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs182692123	chr7:128888117-128888118	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs371020251	chr7:128888243-128888244	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs539057010	chr7:128888305-128888306	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs553950212	chr7:128888350-128888351	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs200854984	chr7:128888351-128888352	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs199997056	chr7:128888352-128888353	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs536361402	chr7:128888363-128888364	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs555158850	chr7:128888364-128888365	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs576715253	chr7:128888454-128888455	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs368617052	chr7:128888461-128888462	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs75305879	chr7:128888473-128888474	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs201616562	chr7:128888496-128888497	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs112032902	chr7:128888538-128888539	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs2896414	chr7:128888544-128888545	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs559336797	chr7:128888594-128888595	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs143607392	chr7:128888604-128888605	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs147971752	chr7:128888624-128888625	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs559108177	chr7:128888650-128888651	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs1918166	chr7:128888673-128888674	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs567480948	chr7:128888693-128888694	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs569552381	chr7:128888733-128888734	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs1918167	chr7:128888762-128888763	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs200064237	chr7:128888826-128888827	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs34696153	chr7:128888837-128888838	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs62480597	chr7:128888857-128888858	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs541535718	chr7:128888953-128888954	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs186886881	chr7:128888957-128888958	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs368569845	chr7:128888962-128888963	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:80)

Disease	PMID	Source
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
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Wilms tumour	21544195	CNVD
T-cell prolymphocytic leukemia	19278963	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
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
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
lymphocytic leukemia	21291569	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
Biliary cancer	19435499	CNVD
Adenocarcinoma	21044232	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Melanoma	19188590	CNVD
Hepatocellular carcinoma	16785998	CNVD
Glioblastoma multiforme	18628472	CNVD
Basal cell lymphoma	21115979	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Malignant melanoma	17260012	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	17217626	CNVD
Coffin-Siris syndrome	21572526	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Retinitis pigmentosa	17160897	CNVD
Colorblindness	17160897	CNVD
Multiple myeloma	16616336	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Bladder cancer	21909424	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:585 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:128866000-128902200	Weak transcription	Gastric	stomach
2	chr7:128866200-128898600	Weak transcription	Thymus	Thymus
3	chr7:128866400-128891400	Weak transcription	Fetal Stomach	stomach
4	chr7:128866400-128899000	Weak transcription	Ovary	ovary
5	chr7:128866600-128901400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
6	chr7:128866800-128889600	Weak transcription	Primary T helper cells fromperipheralblood	blood
7	chr7:128867000-128898400	Weak transcription	Primary T helper cells PMA-I stimulated	--
8	chr7:128867200-128909800	Weak transcription	Primary B cells from cord blood	blood
9	chr7:128868600-128897200	Weak transcription	Sigmoid Colon	Sigmoid Colon
10	chr7:128872800-128892000	Weak transcription	Skeletal Muscle Female	skeletal muscle
11	chr7:128876400-128889800	Weak transcription	Fetal Intestine Small	intestine
12	chr7:128878800-128897000	Weak transcription	Monocytes-CD14+_RO01746	blood
13	chr7:128880400-128889800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
14	chr7:128881000-128892000	Weak transcription	Brain Cingulate Gyrus	brain
15	chr7:128881000-128898800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr7:128882000-128899600	Weak transcription	Left Ventricle	heart
17	chr7:128882200-128888000	Weak transcription	H9 Cell Line	embryonic stem cell
18	chr7:128884400-128888000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
19	chr7:128884800-128898800	Weak transcription	Primary T cells from cord blood	blood
20	chr7:128885000-128887600	Weak transcription	Fetal Heart	heart
21	chr7:128885000-128890000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr7:128885600-128898600	Weak transcription	Brain Germinal Matrix	brain
23	chr7:128886600-128889800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr7:128887200-128887600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr7:128887200-128898600	Weak transcription	NHEK	skin
26	chr7:128887400-128887600	Enhancers	Pancreas	Pancrea
27	chr7:128887400-128888200	Enhancers	HUES48 Cell Line	embryonic stem cell
28	chr7:128887600-128888200	Enhancers	ES-I3 Cell Line	embryonic stem cell
29	chr7:128887600-128892400	Weak transcription	Pancreas	Pancrea
30	chr7:128888000-128888200	Enhancers	H9 Cell Line	embryonic stem cell
31	chr7:128888000-128888200	Enhancers	iPS-15b Cell Line	embryonic stem cell
32	chr7:128888000-128891800	Weak transcription	Brain Anterior Caudate	brain
33	chr7:128888200-128895800	Weak transcription	HUES48 Cell Line	embryonic stem cell
34	chr7:128889800-128890200	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
35	chr7:128889800-128890200	ZNF genes & repeats	Fetal Intestine Small	intestine
36	chr7:128890000-128890200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr7:128890200-128892000	Weak transcription	Fetal Intestine Small	intestine
38	chr7:128890200-128895800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr7:128890800-128892800	Enhancers	Cortex derived primary cultured neurospheres	brain
40	chr7:128890800-128897200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr7:128891200-128897000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
42	chr7:128891400-128891600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
43	chr7:128891400-128891600	Enhancers	Fetal Stomach	stomach
44	chr7:128891600-128892000	Weak transcription	Fetal Stomach	stomach
45	chr7:128891600-128892200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
46	chr7:128891600-128892400	Enhancers	Pancreatic Islets	Pancreatic Islet
47	chr7:128891800-128892400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
48	chr7:128891800-128892400	Enhancers	Brain Anterior Caudate	brain
49	chr7:128891800-128892600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr7:128891800-128892600	Enhancers	Fetal Lung	lung

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