Variant report

Variant	nsv887721
Chromosome Location	chr7:15025332-15163610
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:739)
CpG islands
(count:61)
Chromatin interactive
region (count:15)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:739 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:15055726-15056046	HepG2	liver:	n/a	n/a
2	BACH1	chr7:15051037-15051612	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr7:15136729-15136926	K562	blood:	n/a	n/a
4	BACH1	chr7:15052301-15052317	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr7:15035586-15035785	H1-hESC	embryonic stem cell:	n/a	n/a
6	BHLHE40	chr7:15055727-15055963	GM12878	blood:	n/a	n/a
7	BHLHE40	chr7:15055872-15056060	K562	blood:	n/a	n/a
8	CEBPB	chr7:15107141-15107395	HepG2	liver:	n/a	chr7:15107268-15107279
9	CEBPB	chr7:15107146-15107394	A549	lung:	n/a	chr7:15107268-15107279
10	CEBPB	chr7:15080351-15081311	Hela-S3	cervix:	n/a	chr7:15081129-15081142
11	CEBPB	chr7:15107126-15107433	IMR90	lung:	n/a	chr7:15107268-15107279
12	CEBPB	chr7:15056178-15057050	HCT-116	colon:	n/a	chr7:15056927-15056938
13	CEBPB	chr7:15077096-15077349	HepG2	liver:	n/a	chr7:15077196-15077207
14	CEBPB	chr7:15040679-15040860	HepG2	liver:	n/a	chr7:15040775-15040786 chr7:15040775-15040788
15	CEBPB	chr7:15107136-15107410	Hela-S3	cervix:	n/a	chr7:15107268-15107279
16	CEBPB	chr7:15126038-15126244	HepG2	liver:	n/a	chr7:15126178-15126189
17	CEBPB	chr7:15126055-15126326	IMR90	lung:	n/a	chr7:15126178-15126189
18	CEBPB	chr7:15126040-15126347	Hela-S3	cervix:	n/a	chr7:15126178-15126189
19	CTCF	chr7:15055800-15055950	HMEC	breast:	n/a	chr7:15055896-15055905 chr7:15055892-15055905
20	CTCF	chr7:15047260-15047410	HL-60	blood:	n/a	n/a
21	CTCF	chr7:15055540-15055690	GM12865	blood:	n/a	n/a
22	CTCF	chr7:15055860-15056010	GM12870	blood:	n/a	chr7:15055896-15055905 chr7:15055892-15055905
23	CTCF	chr7:15055820-15055970	GM06990	blood:	n/a	chr7:15055896-15055905 chr7:15055892-15055905
24	CTCF	chr7:15056740-15056890	AG10803	skin:	n/a	n/a
25	CTCF	chr7:15047233-15047375	GM19239	blood:	n/a	n/a
26	CTCF	chr7:15055200-15055350	AG04450	lung:	n/a	n/a
27	CTCF	chr7:15047220-15047370	NB4	blood:	n/a	n/a
28	CTCF	chr7:15047180-15047330	HepG2	liver:	n/a	n/a
29	CTCF	chr7:15055780-15055930	Caco-2	colon:	n/a	chr7:15055896-15055905 chr7:15055892-15055905
30	CTCF	chr7:15055840-15055990	HepG2	liver:	n/a	chr7:15055896-15055905 chr7:15055892-15055905
31	CTCF	chr7:15055080-15055230	GM12866	blood:	n/a	n/a
32	CTCF	chr7:15047160-15047310	GM12866	blood:	n/a	n/a
33	CTCF	chr7:15055840-15055990	GM06990	blood:	n/a	chr7:15055896-15055905 chr7:15055892-15055905
34	CTCF	chr7:15047240-15047390	AG04450	lung:	n/a	n/a
35	CTCF	chr7:15055880-15056030	HRE	kidney:	n/a	chr7:15055896-15055905 chr7:15055892-15055905
36	CTCF	chr7:15047300-15047450	HAc	cerebellar:	n/a	n/a
37	CTCF	chr7:15047188-15047409	Hela-S3	cervix:	n/a	n/a
38	CTCF	chr7:15055720-15055870	RPTEC	kidney:	n/a	n/a
39	CTCF	chr7:15047160-15047310	GM12871	blood:	n/a	n/a
40	CTCF	chr7:15055764-15056048	GM12878	blood:	n/a	chr7:15055896-15055905 chr7:15055892-15055905
41	CTCF	chr7:15055280-15055430	HFF	foreskin:	n/a	n/a
42	CTCF	chr7:15055800-15055950	GM12871	blood:	n/a	chr7:15055896-15055905 chr7:15055892-15055905
43	CTCF	chr7:15047180-15047330	GM12869	blood:	n/a	n/a
44	CTCF	chr7:15047260-15047410	HCM	heart:	n/a	n/a
45	CTCF	chr7:15055820-15055970	HRPEpiC	eye:	n/a	chr7:15055896-15055905 chr7:15055892-15055905
46	CTCF	chr7:15055840-15055990	HCT-116	colon:	n/a	chr7:15055896-15055905 chr7:15055892-15055905
47	CTCF	chr7:15055820-15055970	AG04449	skin:	n/a	chr7:15055896-15055905 chr7:15055892-15055905
48	CTCF	chr7:15046920-15047070	HMF	breast:	n/a	n/a
49	CTCF	chr7:15055840-15055990	WERI-Rb-1	eye:	n/a	chr7:15055896-15055905 chr7:15055892-15055905
50	CTCF	chr7:15047260-15047410	RPTEC	kidney:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:15055459-15055509	AG09319	gingival:	n/a
2	chr7:15055459-15055509	GM12878	blood:	n/a
3	chr7:15055459-15055509	H1-hESC	embryonic stem cell:	embryo
4	chr7:15055459-15055509	BJ	skin:	n/a
5	chr7:15055459-15055509	Jurkat	blood:	n/a
6	chr7:15055459-15055509	Hela-S3	cervix:	n/a
7	chr7:15055459-15055509	HAEpiC	amniotic membrane:	n/a
8	chr7:15055459-15055509	GM06990	blood:	n/a
9	chr7:15055459-15055509	HEK293	kidney:	embryo
10	chr7:15055459-15055509	HRCEpiC	kidney:	n/a
11	chr7:15055459-15055509	NHBE	bronchial:	n/a
12	chr7:15055459-15055509	U87	brain:	n/a
13	chr7:15055459-15055509	HCPEpiC	choroid plexus:	n/a
14	chr7:15055459-15055509	IMR90	lung:	fetal
15	chr7:15055459-15055509	NB4	blood:	n/a
16	chr7:15055459-15055509	HPAEpiC	pulmonary alveolar:	n/a
17	chr7:15055459-15055509	HCM	heart:	n/a
18	chr7:15055459-15055509	SAEC	small airway:	n/a
19	chr7:15055459-15055509	NT2-D1	testis:	n/a
20	chr7:15055459-15055509	AG04449	skin:	fetal
21	chr7:15055459-15055509	AoSMC	blood vessel:	n/a
22	chr7:15055459-15055509	Hepatocyte	liver:	n/a
23	chr7:15055459-15055509	HMEC	breast:	n/a
24	chr7:15055459-15055509	HUVEC	blood vessel:	n/a
25	chr7:15055459-15055509	ECC-1	luminal epithelium:	n/a
26	chr7:15055459-15055509	GM19239	blood:	n/a
27	chr7:15055459-15055509	NH-A	brain:	n/a
28	chr7:15055459-15055509	NHDF-neo	bronchial:	n/a
29	chr7:15055459-15055509	ProgFib	skin:	n/a
30	chr7:15055459-15055509	LNCaP	prostate:	n/a
31	chr7:15055459-15055509	HCF	heart:	n/a
32	chr7:15055459-15055509	HIPEpiC	eye:	n/a
33	chr7:15055459-15055509	PrEC	prostate:	n/a
34	chr7:15055459-15055509	MCF-7	breast:	n/a
35	chr7:15055459-15055509	HRE	kidney:	n/a
36	chr7:15055459-15055509	A549	lung:	n/a
37	chr7:15055459-15055509	GM12891	blood:	n/a
38	chr7:15055459-15055509	SK-N-SH	brain:	n/a
39	chr7:15055459-15055509	GM12892	blood:	n/a
40	chr7:15055459-15055509	CMK	blood:	n/a
41	chr7:15055459-15055509	SK-N-MC	brain:	n/a
42	chr7:15055459-15055509	HL-60	blood:	n/a
43	chr7:15055459-15055509	MCF10A-Er-Src	breast:	n/a
44	chr7:15055459-15055509	RPTEC	kidney:	n/a
45	chr7:15055459-15055509	HNPCEpiC	eye:	n/a
46	chr7:15055459-15055509	PFSK-1	brain:	n/a
47	chr7:15055459-15055509	AG04450	lung:	fetal
48	chr7:15055459-15055509	HepG2	liver:	n/a
49	chr7:15055459-15055509	BE2_C	brain:	n/a
50	chr7:15055459-15055509	T-47D	breast:	n/a

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:10529800..10530510-chr7:15146578..15147089,2	MCF-7	breast:
2	chr7:13317591..13319993-chr7:15056107..15057980,2	K562	blood:
3	chr7:15033798..15035958-chr7:15043965..15046706,2	K562	blood:
4	chr7:15058053..15060763-chr7:15070842..15072885,2	K562	blood:
5	chr7:15058053..15060763-chr7:15070842..15072885,2	K562	blood:
6	chr7:15046835..15047773-chr7:15055487..15056275,2	MCF-7	breast:
7	chr7:15148394..15150106-chr7:15160727..15163235,2	K562	blood:
8	chr7:14757467..14758291-chr7:15055705..15056411,2	MCF-7	breast:
9	chr7:14737644..14738448-chr7:15055761..15056392,2	MCF-7	breast:
10	chr7:15148394..15150106-chr7:15160727..15163235,2	K562	blood:
11	chr7:14756304..14757028-chr7:15055834..15056611,2	MCF-7	breast:
12	chr7:14757081..14758001-chr7:15054605..15056087,5	MCF-7	breast:
13	chr7:15033798..15035958-chr7:15043965..15046706,2	K562	blood:
14	chr7:15046835..15047773-chr7:15055487..15056275,2	MCF-7	breast:
15	chr7:15003480..15005257-chr7:15044429..15047091,2	K562	blood:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC006035.2-4	chr7:15107930-15108276	XLOC_005990
2	lnc-AC006035.2-9	chr7:15072357-15072662	NONHSAT119273
3	lnc-AC006035.2-9	chr7:15074455-15074801	NONHSAT119273
4	lnc-DGKB-1	chr7:15025003-15025699	NONHSAT119271
5	lnc-AC006035.2-4	chr7:15105832-15106137	XLOC_005990

No data

Variant related genes	Relation type
ENSG00000225816	TF binding region
ENSG00000227489	TF binding region
ENSG00000225816	CpG island
ENSG00000227489	CpG island
ENSG00000111846	chromatin interactions

Extended variants
information (count: 3561 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:3561 , 50 per page) page: 1 2 3 4 5 6 7 ... 72

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs917037	chr7:15025332-15025333	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs550409490	chr7:15025362-15025363	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
3	rs546333108	chr7:15025384-15025385	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
4	rs12375103	chr7:15025396-15025397	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs183863794	chr7:15025422-15025423	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
6	rs552756021	chr7:15025447-15025448	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
7	rs544943548	chr7:15025499-15025500	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
8	rs566481511	chr7:15025509-15025510	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
9	rs538207066	chr7:15025514-15025515	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
10	rs558497043	chr7:15025558-15025559	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
11	rs578260002	chr7:15025600-15025601	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
12	rs183304702	chr7:15025625-15025626	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
13	rs541028301	chr7:15025626-15025627	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
14	rs376888489	chr7:15025640-15025641	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
15	rs116252950	chr7:15025643-15025644	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
16	rs373118326	chr7:15025669-15025670	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
17	rs557615700	chr7:15025680-15025681	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
18	rs183042759	chr7:15028326-15028327	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs28669231	chr7:15028350-15028351	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs192558442	chr7:15028364-15028365	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs375335279	chr7:15028445-15028446	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs142193310	chr7:15028447-15028448	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs376175793	chr7:15028461-15028462	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs55901722	chr7:15028489-15028490	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs113057329	chr7:15028508-15028509	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs547840195	chr7:15028529-15028530	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs570847134	chr7:15028550-15028551	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs539762275	chr7:15028551-15028552	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs556471234	chr7:15028589-15028590	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs117561789	chr7:15028631-15028632	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs372490978	chr7:15028651-15028652	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs10282014	chr7:15028655-15028656	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs535594821	chr7:15028676-15028677	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs374832587	chr7:15028714-15028715	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs555260471	chr7:15028718-15028719	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs572149799	chr7:15028744-15028745	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs142987207	chr7:15028761-15028762	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs544045105	chr7:15028773-15028774	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs563772998	chr7:15028793-15028794	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs577183673	chr7:15028808-15028809	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs546108861	chr7:15028832-15028833	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs561023420	chr7:15028882-15028883	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs56041358	chr7:15028899-15028900	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs79469283	chr7:15028901-15028902	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs73062803	chr7:15028903-15028904	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs562122231	chr7:15028917-15028918	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs151137614	chr7:15028930-15028931	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs547878979	chr7:15028948-15028949	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs562985639	chr7:15028957-15028958	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs113472626	chr7:15028959-15028960	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:81)

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
Myelofibrosis	22110671	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Glioblastoma multiforme	18628472	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:307 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:15039000-15040600	Enhancers	Liver	Liver
2	chr7:15039600-15040000	Enhancers	HepG2	liver
3	chr7:15047000-15048200	Enhancers	Liver	Liver
4	chr7:15047400-15047600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr7:15047600-15055000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr7:15049400-15049600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
7	chr7:15049600-15055000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr7:15050600-15051000	Enhancers	iPS-18 Cell Line	embryonic stem cell
9	chr7:15050600-15051600	Enhancers	HUES64 Cell Line	embryonic stem cell
10	chr7:15050800-15051200	Enhancers	H1 Cell Line	embryonic stem cell
11	chr7:15050800-15051200	Enhancers	iPS-20b Cell Line	embryonic stem cell
12	chr7:15050800-15051800	Enhancers	HUES6 Cell Line	embryonic stem cell
13	chr7:15050800-15052000	Enhancers	H9 Cell Line	embryonic stem cell
14	chr7:15051000-15051400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
15	chr7:15051000-15051800	Enhancers	ES-I3 Cell Line	embryonic stem cell
16	chr7:15051200-15051600	Enhancers	HUES48 Cell Line	embryonic stem cell
17	chr7:15051200-15051600	Enhancers	iPS-15b Cell Line	embryonic stem cell
18	chr7:15051200-15052800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr7:15051200-15054800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
20	chr7:15051400-15051600	Enhancers	iPS-18 Cell Line	embryonic stem cell
21	chr7:15051600-15052200	Enhancers	Skeletal Muscle Male	skeletal muscle
22	chr7:15051600-15052200	Enhancers	Skeletal Muscle Female	skeletal muscle
23	chr7:15051600-15054400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
24	chr7:15051600-15054800	Weak transcription	HUES64 Cell Line	embryonic stem cell
25	chr7:15051600-15054800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
26	chr7:15051600-15055000	Weak transcription	HUES48 Cell Line	embryonic stem cell
27	chr7:15051800-15052200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr7:15051800-15055000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
29	chr7:15051800-15055000	Weak transcription	HUES6 Cell Line	embryonic stem cell
30	chr7:15052000-15052200	Enhancers	Right Ventricle	heart
31	chr7:15052000-15055000	Weak transcription	H9 Cell Line	embryonic stem cell
32	chr7:15052200-15052400	Enhancers	Left Ventricle	heart
33	chr7:15052200-15054200	Weak transcription	Skeletal Muscle Male	skeletal muscle
34	chr7:15052200-15055000	Weak transcription	Skeletal Muscle Female	skeletal muscle
35	chr7:15052200-15055200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr7:15052200-15055200	Weak transcription	Right Ventricle	heart
37	chr7:15052800-15055000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr7:15054000-15054200	Enhancers	Psoas Muscle	Psoas
39	chr7:15054200-15054400	Enhancers	Skeletal Muscle Male	skeletal muscle
40	chr7:15054400-15054800	Weak transcription	Skeletal Muscle Male	skeletal muscle
41	chr7:15054400-15055000	Enhancers	iPS-15b Cell Line	embryonic stem cell
42	chr7:15054800-15055000	Enhancers	HUES64 Cell Line	embryonic stem cell
43	chr7:15054800-15055000	Enhancers	iPS-18 Cell Line	embryonic stem cell
44	chr7:15054800-15055000	Enhancers	iPS-20b Cell Line	embryonic stem cell
45	chr7:15054800-15055200	Enhancers	Skeletal Muscle Male	skeletal muscle
46	chr7:15055000-15055200	Flanking Active TSS	H1 Cell Line	embryonic stem cell
47	chr7:15055000-15055200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
48	chr7:15055000-15055200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
49	chr7:15055000-15055200	Flanking Active TSS	H9 Cell Line	embryonic stem cell
50	chr7:15055000-15055200	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell

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