Variant report

Variant	nsv606297
Chromosome Location	chr7:15582208-15621650
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:15601586-15601746	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:15595136-15595490	HepG2	liver:	n/a	n/a
3	CEBPB	chr7:15595235-15595599	HepG2	liver:	n/a	chr7:15595421-15595430 chr7:15595421-15595430 chr7:15595420-15595431 chr7:15595419-15595432 chr7:15595421-15595430
4	CEBPB	chr7:15604558-15604764	HepG2	liver:	n/a	n/a
5	CEBPB	chr7:15595284-15595549	H1-hESC	embryonic stem cell:	n/a	chr7:15595421-15595430 chr7:15595421-15595430 chr7:15595420-15595431 chr7:15595419-15595432 chr7:15595421-15595430
6	CEBPB	chr7:15595233-15595593	IMR90	lung:	n/a	chr7:15595421-15595430 chr7:15595421-15595430 chr7:15595420-15595431 chr7:15595419-15595432 chr7:15595421-15595430
7	CEBPB	chr7:15595241-15595557	K562	blood:	n/a	chr7:15595421-15595430 chr7:15595421-15595430 chr7:15595420-15595431 chr7:15595419-15595432 chr7:15595421-15595430
8	CEBPB	chr7:15595280-15595609	MCF-7	breast:	n/a	chr7:15595421-15595430 chr7:15595421-15595430 chr7:15595420-15595431 chr7:15595419-15595432 chr7:15595421-15595430
9	CEBPB	chr7:15595210-15595569	ECC-1	luminal epithelium:	n/a	chr7:15595421-15595430 chr7:15595421-15595430 chr7:15595420-15595431 chr7:15595419-15595432 chr7:15595421-15595430
10	CEBPB	chr7:15595255-15595534	ECC-1	luminal epithelium:	n/a	chr7:15595421-15595430 chr7:15595421-15595430 chr7:15595420-15595431 chr7:15595419-15595432 chr7:15595421-15595430
11	CEBPB	chr7:15602402-15602602	A549	lung:	n/a	n/a
12	CEBPB	chr7:15602458-15602740	IMR90	lung:	n/a	n/a
13	CEBPB	chr7:15583840-15584031	HepG2	liver:	n/a	chr7:15583872-15583883
14	CEBPB	chr7:15595204-15595566	A549	lung:	n/a	chr7:15595421-15595430 chr7:15595421-15595430 chr7:15595420-15595431 chr7:15595419-15595432 chr7:15595421-15595430
15	CEBPB	chr7:15595000-15595694	A549	lung:	n/a	chr7:15595421-15595430 chr7:15595421-15595430 chr7:15595420-15595431 chr7:15595419-15595432 chr7:15595421-15595430
16	CEBPB	chr7:15595158-15595630	A549	lung:	n/a	chr7:15595421-15595430 chr7:15595421-15595430 chr7:15595420-15595431 chr7:15595419-15595432 chr7:15595421-15595430
17	CHD2	chr7:15620713-15620886	GM12878	blood:	n/a	n/a
18	CTCF	chr7:15601760-15601910	RPTEC	kidney:	n/a	n/a
19	CTCF	chr7:15595020-15595170	Caco-2	colon:	n/a	chr7:15595087-15595095 chr7:15595083-15595099 chr7:15595077-15595098 chr7:15595084-15595097 chr7:15595082-15595100
20	CTCF	chr7:15595000-15595150	AG10803	skin:	n/a	chr7:15595087-15595095 chr7:15595083-15595099 chr7:15595077-15595098 chr7:15595084-15595097 chr7:15595082-15595100
21	CTCF	chr7:15595000-15595150	MCF-7	breast:	n/a	chr7:15595087-15595095 chr7:15595083-15595099 chr7:15595077-15595098 chr7:15595084-15595097 chr7:15595082-15595100
22	CTCF	chr7:15594980-15595130	A549	lung:	n/a	chr7:15595087-15595095 chr7:15595083-15595099 chr7:15595077-15595098 chr7:15595084-15595097 chr7:15595082-15595100
23	CTCF	chr7:15595000-15595150	HRE	kidney:	n/a	chr7:15595087-15595095 chr7:15595083-15595099 chr7:15595077-15595098 chr7:15595084-15595097 chr7:15595082-15595100
24	CTCF	chr7:15601680-15601830	AG09319	gingival:	n/a	n/a
25	CTCF	chr7:15601860-15602010	RPTEC	kidney:	n/a	n/a
26	CTCF	chr7:15594933-15595264	GM12878	blood:	n/a	chr7:15595087-15595095 chr7:15595083-15595099 chr7:15595077-15595098 chr7:15595084-15595097 chr7:15595082-15595100
27	CTCF	chr7:15598900-15599050	RPTEC	kidney:	n/a	n/a
28	CTCF	chr7:15594980-15595130	HMF	breast:	n/a	chr7:15595087-15595095 chr7:15595083-15595099 chr7:15595077-15595098 chr7:15595084-15595097 chr7:15595082-15595100
29	CTCF	chr7:15595020-15595170	HCFaa	heart:	n/a	chr7:15595087-15595095 chr7:15595083-15595099 chr7:15595077-15595098 chr7:15595084-15595097 chr7:15595082-15595100
30	CTCF	chr7:15599240-15599390	HRE	kidney:	n/a	n/a
31	CTCF	chr7:15595020-15595170	HRPEpiC	eye:	n/a	chr7:15595087-15595095 chr7:15595083-15595099 chr7:15595077-15595098 chr7:15595084-15595097 chr7:15595082-15595100
32	CTCF	chr7:15595020-15595170	RPTEC	kidney:	n/a	chr7:15595087-15595095 chr7:15595083-15595099 chr7:15595077-15595098 chr7:15595084-15595097 chr7:15595082-15595100
33	CTCF	chr7:15601680-15601830	A549	lung:	n/a	n/a
34	CTCF	chr7:15594940-15595090	RPTEC	kidney:	n/a	n/a
35	CTCF	chr7:15595040-15595190	HEEpiC	esophagus:	n/a	chr7:15595087-15595095 chr7:15595083-15595099 chr7:15595077-15595098 chr7:15595084-15595097 chr7:15595082-15595100
36	CTCF	chr7:15595000-15595150	Caco-2	colon:	n/a	chr7:15595087-15595095 chr7:15595083-15595099 chr7:15595077-15595098 chr7:15595084-15595097 chr7:15595082-15595100
37	CTCF	chr7:15601720-15601870	HMF	breast:	n/a	n/a
38	CTCF	chr7:15595000-15595150	HBMEC	blood vessel:	n/a	chr7:15595087-15595095 chr7:15595083-15595099 chr7:15595077-15595098 chr7:15595084-15595097 chr7:15595082-15595100
39	CTCF	chr7:15595020-15595170	SK-N-SH_RA	brain:	n/a	chr7:15595087-15595095 chr7:15595083-15595099 chr7:15595077-15595098 chr7:15595084-15595097 chr7:15595082-15595100
40	CTCF	chr7:15595000-15595150	HPAF	blood vessel:	n/a	chr7:15595087-15595095 chr7:15595083-15595099 chr7:15595077-15595098 chr7:15595084-15595097 chr7:15595082-15595100
41	CTCF	chr7:15594940-15595090	BE2_C	brain:	n/a	n/a
42	CTCF	chr7:15595000-15595150	AoAF	blood vessel:	n/a	chr7:15595087-15595095 chr7:15595083-15595099 chr7:15595077-15595098 chr7:15595084-15595097 chr7:15595082-15595100
43	CTCF	chr7:15601684-15601753	A549	lung:	n/a	n/a
44	CTCF	chr7:15594900-15595050	HFF	foreskin:	n/a	n/a
45	CTCF	chr7:15601680-15601830	HMF	breast:	n/a	n/a
46	CTCF	chr7:15601623-15601907	GM12878	blood:	n/a	n/a
47	CTCF	chr7:15601715-15601853	Kidney_OC	kidney:	n/a	n/a
48	CTCF	chr7:15595040-15595190	HCM	heart:	n/a	chr7:15595087-15595095 chr7:15595083-15595099 chr7:15595077-15595098 chr7:15595084-15595097 chr7:15595082-15595100
49	CTCF	chr7:15594980-15595130	AG04450	lung:	n/a	chr7:15595087-15595095 chr7:15595083-15595099 chr7:15595077-15595098 chr7:15595084-15595097 chr7:15595082-15595100
50	CTCF	chr7:15601701-15601815	Pancreas_OC	pancreas:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:15601624-15601674	GM12891	blood:	n/a
2	chr7:15601624-15601674	GM12891	blood:	n/a
3	chr7:15587184-15587234	LNCaP	prostate:	n/a
4	chr7:15587184-15587234	HEEpiC	esophagus:	n/a
5	chr7:15601624-15601674	SK-N-MC	brain:	n/a
6	chr7:15601624-15601674	HCF	heart:	n/a
7	chr7:15587184-15587234	SAEC	small airway:	n/a
8	chr7:15601624-15601674	HEK293	kidney:	embryo
9	chr7:15587184-15587234	GM12891	blood:	n/a
10	chr7:15587184-15587234	ProgFib	skin:	n/a
11	chr7:15601624-15601674	AG04449	skin:	fetal
12	chr7:15587184-15587234	SK-N-SH_RA	brain:	n/a
13	chr7:15587184-15587234	NT2-D1	testis:	n/a
14	chr7:15601624-15601674	T-47D	breast:	n/a
15	chr7:15601624-15601674	K562	blood:	n/a
16	chr7:15587184-15587234	GM12878	blood:	n/a
17	chr7:15587184-15587234	AG09319	gingival:	n/a
18	chr7:15587184-15587234	GM19239	blood:	n/a
19	chr7:15587184-15587234	AG10803	skin:	n/a
20	chr7:15601624-15601674	SAEC	small airway:	n/a
21	chr7:15601624-15601674	PrEC	prostate:	n/a
22	chr7:15601624-15601674	PFSK-1	brain:	n/a
23	chr7:15601624-15601674	ECC-1	luminal epithelium:	n/a
24	chr7:15601624-15601674	Hepatocyte	liver:	n/a
25	chr7:15587184-15587234	HRCEpiC	kidney:	n/a
26	chr7:15601624-15601674	RPTEC	kidney:	n/a
27	chr7:15587184-15587234	SK-N-MC	brain:	n/a
28	chr7:15587184-15587234	AG09309	skin:	n/a
29	chr7:15587184-15587234	BE2_C	brain:	n/a
30	chr7:15601624-15601674	HEEpiC	esophagus:	n/a
31	chr7:15601624-15601674	SKMC	muscle:	n/a
32	chr7:15601624-15601674	GM19239	blood:	n/a
33	chr7:15587184-15587234	HRPEpiC	eye:	n/a
34	chr7:15587184-15587234	Jurkat	blood:	n/a
35	chr7:15587184-15587234	T-47D	breast:	n/a
36	chr7:15587184-15587234	RPTEC	kidney:	n/a
37	chr7:15587184-15587234	U87	brain:	n/a
38	chr7:15587184-15587234	HNPCEpiC	eye:	n/a
39	chr7:15587184-15587234	HCPEpiC	choroid plexus:	n/a
40	chr7:15587184-15587234	HEK293	kidney:	embryo
41	chr7:15601624-15601674	CMK	blood:	n/a
42	chr7:15587184-15587234	AG04449	skin:	fetal
43	chr7:15601624-15601674	HCPEpiC	choroid plexus:	n/a
44	chr7:15587184-15587234	SKMC	muscle:	n/a
45	chr7:15587184-15587234	HRE	kidney:	n/a
46	chr7:15601624-15601674	HUVEC	blood vessel:	n/a
47	chr7:15601624-15601674	H1-hESC	embryonic stem cell:	embryo
48	chr7:15587184-15587234	HCF	heart:	n/a
49	chr7:15601624-15601674	Hela-S3	cervix:	n/a
50	chr7:15587184-15587234	PFSK-1	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:15583030..15584744-chr7:15618985..15621103,2	K562	blood:
2	chr7:15611475..15614112-chr7:15875900..15877965,2	K562	blood:
3	chr7:15583030..15584744-chr7:15618985..15621103,2	K562	blood:
4	chr7:15365462..15366327-chr7:15594881..15595525,2	MCF-7	breast:
5	chr7:15365402..15367803-chr7:15593636..15595869,2	MCF-7	breast:

Variant related genes	Relation type
AGMO	TF binding region
AGMO	CpG island

Extended variants
information (count: 1438 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:1438 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2196395	chr7:15582208-15582209	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs375047690	chr7:15582228-15582229	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs555630466	chr7:15582270-15582271	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs112235825	chr7:15582290-15582291	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs538180769	chr7:15582295-15582296	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs16878529	chr7:15582304-15582305	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs369159476	chr7:15582365-15582366	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs542837173	chr7:15582367-15582368	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs143796462	chr7:15582374-15582375	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs186795983	chr7:15582384-15582385	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs529039309	chr7:15582393-15582394	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs372685573	chr7:15582400-15582401	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs561188513	chr7:15582432-15582433	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs531882281	chr7:15582433-15582434	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs114281206	chr7:15582483-15582484	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs190225638	chr7:15582507-15582508	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs532907064	chr7:15582581-15582582	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs17168818	chr7:15582592-15582593	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs151113796	chr7:15582608-15582609	Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs577386732	chr7:15582622-15582623	Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs559622307	chr7:15582626-15582627	Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs549188969	chr7:15582627-15582628	Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs77268968	chr7:15582636-15582637	Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs553393470	chr7:15582680-15582681	Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs556380351	chr7:15582754-15582755	Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs73679649	chr7:15582767-15582768	Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs73679650	chr7:15582784-15582785	Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs73679651	chr7:15582788-15582789	Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs575760918	chr7:15582809-15582810	Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs370579429	chr7:15582870-15582871	Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs140139843	chr7:15582873-15582874	Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs544463886	chr7:15582909-15582910	Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs542762001	chr7:15582933-15582934	Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs117570305	chr7:15582936-15582937	Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs576191422	chr7:15582946-15582947	Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs543625532	chr7:15582970-15582971	Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs150291017	chr7:15582971-15582972	Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs543849395	chr7:15583048-15583049	Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs17168820	chr7:15583088-15583089	Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs559931917	chr7:15583111-15583112	Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs79872496	chr7:15583123-15583124	Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs549052175	chr7:15583131-15583132	Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs371942059	chr7:15583144-15583145	Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs567377715	chr7:15583156-15583157	Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs531496862	chr7:15583161-15583162	Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs375221431	chr7:15583178-15583179	Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs7802433	chr7:15583180-15583181	Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs376766460	chr7:15583247-15583248	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs538588739	chr7:15583278-15583279	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs554135634	chr7:15583280-15583281	Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:84)

Disease	PMID	Source
Melanoma	18172304	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
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Autism	22495311	CNVD
Prostate cancer	16573809	CNVD
Acute myeloid leukemia	21251322	CNVD
Melanoma	17363583	CNVD
Kartagener syndrome	16639409	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	19242612	CNVD
Autism	18414403	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21858162	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Cancer	21637783	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16397240	CNVD
Non-small cell lung cancer	21829676	CNVD
Glioblastoma multiforme	17002787	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Glioblastoma multiforme	18628472	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Heart disease	21282601	CNVD
Rubinstein-Taybi syndrome	22470819	CNVD
Alzheimer''s disease	22166940	CNVD
Abnormal phenotypes	18644119	CNVD
Non-syndromic sensorineural hearing loss	22570644	CNVD
Bladder cancer	21909424	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:369 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:15580200-15582600	Weak transcription	Liver	Liver
2	chr7:15582600-15583000	Enhancers	Fetal Brain Male	brain
3	chr7:15582600-15583200	Enhancers	Cortex derived primary cultured neurospheres	brain
4	chr7:15582600-15583800	Strong transcription	Liver	Liver
5	chr7:15582800-15583200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
6	chr7:15583800-15586000	Weak transcription	Liver	Liver
7	chr7:15585800-15586400	Enhancers	HUES6 Cell Line	embryonic stem cell
8	chr7:15586000-15586200	Enhancers	ES-I3 Cell Line	embryonic stem cell
9	chr7:15586000-15586200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr7:15586000-15586400	Enhancers	HUES48 Cell Line	embryonic stem cell
11	chr7:15586000-15586400	Enhancers	Liver	Liver
12	chr7:15586000-15586600	Enhancers	H1 Cell Line	embryonic stem cell
13	chr7:15586000-15586600	Enhancers	iPS-18 Cell Line	embryonic stem cell
14	chr7:15586000-15587200	Active TSS	iPS-15b Cell Line	embryonic stem cell
15	chr7:15586200-15586600	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
16	chr7:15586200-15586600	Enhancers	H9 Cell Line	embryonic stem cell
17	chr7:15586400-15586800	Active TSS	ES-WA7 Cell Line	embryonic stem cell
18	chr7:15586400-15586800	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
19	chr7:15586400-15586800	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
20	chr7:15586400-15586800	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
21	chr7:15586600-15586800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
22	chr7:15586600-15587200	Active TSS	HUES64 Cell Line	embryonic stem cell
23	chr7:15586600-15587400	Active TSS	ES-I3 Cell Line	embryonic stem cell
24	chr7:15586600-15587400	Active TSS	H1 Cell Line	embryonic stem cell
25	chr7:15586800-15587400	Active TSS	H9 Cell Line	embryonic stem cell
26	chr7:15586800-15587400	Active TSS	HUES48 Cell Line	embryonic stem cell
27	chr7:15586800-15587400	Active TSS	HUES6 Cell Line	embryonic stem cell
28	chr7:15586800-15587400	Active TSS	iPS-18 Cell Line	embryonic stem cell
29	chr7:15593000-15593400	Weak transcription	Liver	Liver
30	chr7:15593000-15594600	Enhancers	Fetal Intestine Small	intestine
31	chr7:15593000-15596800	Enhancers	HUVEC	blood vessel
32	chr7:15593400-15593600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
33	chr7:15593400-15593600	Enhancers	Liver	Liver
34	chr7:15593400-15593600	Flanking Active TSS	A549	lung
35	chr7:15593400-15594000	Enhancers	iPS-20b Cell Line	embryonic stem cell
36	chr7:15593400-15594000	Enhancers	HSMM	muscle
37	chr7:15593400-15594200	Enhancers	ES-I3 Cell Line	embryonic stem cell
38	chr7:15593400-15594200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
39	chr7:15593400-15594200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
40	chr7:15593400-15594200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
41	chr7:15593400-15594400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
42	chr7:15593400-15594600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
43	chr7:15593400-15594800	Enhancers	Brain Substantia Nigra	brain
44	chr7:15593400-15595400	Enhancers	Osteobl	bone
45	chr7:15593400-15596400	Enhancers	NHDF-Ad	bronchial
46	chr7:15593400-15600600	Enhancers	Muscle Satellite Cultured Cells	--
47	chr7:15593600-15593800	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
48	chr7:15593600-15593800	Flanking Active TSS	Liver	Liver
49	chr7:15593600-15593800	Enhancers	Brain Angular Gyrus	brain
50	chr7:15593600-15593800	Active TSS	A549	lung

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