Variant report

Variant	nsv1018434
Chromosome Location	chr7:15054190-15144078
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	chr7:15055726-15056046	HepG2	liver:	n/a	n/a
2	BACH1	chr7:15136729-15136926	K562	blood:	n/a	n/a
3	BHLHE40	chr7:15055872-15056060	K562	blood:	n/a	n/a
4	BHLHE40	chr7:15055727-15055963	GM12878	blood:	n/a	n/a
5	CEBPB	chr7:15077096-15077349	HepG2	liver:	n/a	chr7:15077196-15077207
6	CEBPB	chr7:15107136-15107410	Hela-S3	cervix:	n/a	chr7:15107268-15107279
7	CEBPB	chr7:15107141-15107395	HepG2	liver:	n/a	chr7:15107268-15107279
8	CEBPB	chr7:15107126-15107433	IMR90	lung:	n/a	chr7:15107268-15107279
9	CEBPB	chr7:15126055-15126326	IMR90	lung:	n/a	chr7:15126178-15126189
10	CEBPB	chr7:15126038-15126244	HepG2	liver:	n/a	chr7:15126178-15126189
11	CEBPB	chr7:15107146-15107394	A549	lung:	n/a	chr7:15107268-15107279
12	CEBPB	chr7:15126040-15126347	Hela-S3	cervix:	n/a	chr7:15126178-15126189
13	CEBPB	chr7:15056178-15057050	HCT-116	colon:	n/a	chr7:15056927-15056938
14	CEBPB	chr7:15080351-15081311	Hela-S3	cervix:	n/a	chr7:15081129-15081142
15	CTCF	chr7:15055786-15055985	HepG2	liver:	n/a	chr7:15055896-15055905 chr7:15055892-15055905
16	CTCF	chr7:15055802-15055962	A549	lung:	n/a	chr7:15055896-15055905 chr7:15055892-15055905
17	CTCF	chr7:15055200-15055350	GM12873	blood:	n/a	n/a
18	CTCF	chr7:15055820-15055970	HMF	breast:	n/a	chr7:15055896-15055905 chr7:15055892-15055905
19	CTCF	chr7:15055820-15055970	AG10803	skin:	n/a	chr7:15055896-15055905 chr7:15055892-15055905
20	CTCF	chr7:15055760-15056036	Medullo	brain:	n/a	chr7:15055896-15055905 chr7:15055892-15055905
21	CTCF	chr7:15055840-15055990	WERI-Rb-1	eye:	n/a	chr7:15055896-15055905 chr7:15055892-15055905
22	CTCF	chr7:15055840-15055990	SK-N-SH_RA	brain:	n/a	chr7:15055896-15055905 chr7:15055892-15055905
23	CTCF	chr7:15055781-15056023	GM13977	blood:	n/a	chr7:15055896-15055905 chr7:15055892-15055905
24	CTCF	chr7:15056513-15056562	GM20000	blood:	n/a	n/a
25	CTCF	chr7:15055478-15056261	A549	lung:	n/a	chr7:15055896-15055905 chr7:15055892-15055905
26	CTCF	chr7:15055880-15056030	HRE	kidney:	n/a	chr7:15055896-15055905 chr7:15055892-15055905
27	CTCF	chr7:15055726-15056073	K562	blood:	n/a	chr7:15055896-15055905 chr7:15055892-15055905
28	CTCF	chr7:15055860-15056010	GM12875	blood:	n/a	chr7:15055896-15055905 chr7:15055892-15055905
29	CTCF	chr7:15055720-15055870	HFF-Myc	foreskin:	n/a	n/a
30	CTCF	chr7:15055220-15055370	GM12873	blood:	n/a	n/a
31	CTCF	chr7:15055820-15055970	GM12875	blood:	n/a	chr7:15055896-15055905 chr7:15055892-15055905
32	CTCF	chr7:15055680-15055950	NHDF-neo	bronchial:	n/a	chr7:15055896-15055905 chr7:15055892-15055905
33	CTCF	chr7:15055820-15055970	AG09309	skin:	n/a	chr7:15055896-15055905 chr7:15055892-15055905
34	CTCF	chr7:15055806-15055992	GM13976	blood:	n/a	chr7:15055896-15055905 chr7:15055892-15055905
35	CTCF	chr7:15055620-15056151	MCF-7	breast:	n/a	chr7:15055896-15055905 chr7:15055892-15055905
36	CTCF	chr7:15055860-15056010	NB4	blood:	n/a	chr7:15055896-15055905 chr7:15055892-15055905
37	CTCF	chr7:15055800-15055950	AG04450	lung:	n/a	chr7:15055896-15055905 chr7:15055892-15055905
38	CTCF	chr7:15055840-15055990	GM12878	blood:	n/a	chr7:15055896-15055905 chr7:15055892-15055905
39	CTCF	chr7:15055540-15055690	GM12865	blood:	n/a	n/a
40	CTCF	chr7:15055667-15056082	A549	lung:	n/a	chr7:15055896-15055905 chr7:15055892-15055905
41	CTCF	chr7:15055820-15055970	NHLF	lung:	n/a	chr7:15055896-15055905 chr7:15055892-15055905
42	CTCF	chr7:15055533-15056132	HCT-116	colon:	n/a	chr7:15055896-15055905 chr7:15055892-15055905
43	CTCF	chr7:15055780-15055930	Caco-2	colon:	n/a	chr7:15055896-15055905 chr7:15055892-15055905
44	CTCF	chr7:15055793-15056048	GM10266	blood:	n/a	chr7:15055896-15055905 chr7:15055892-15055905
45	CTCF	chr7:15055795-15055948	NHEK	skin:	n/a	chr7:15055896-15055905 chr7:15055892-15055905
46	CTCF	chr7:15055776-15056017	Gliobla	brain:	n/a	chr7:15055896-15055905 chr7:15055892-15055905
47	CTCF	chr7:15055763-15056057	HUVEC	blood vessel:	n/a	chr7:15055896-15055905 chr7:15055892-15055905
48	CTCF	chr7:15055760-15055910	HA-sp	spinal cord:	n/a	chr7:15055896-15055905 chr7:15055892-15055905
49	CTCF	chr7:15055820-15055970	GM12874	blood:	n/a	chr7:15055896-15055905 chr7:15055892-15055905
50	CTCF	chr7:15055700-15055850	A549	lung:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:15055459-15055509	Caco-2	colon:	n/a
2	chr7:15055459-15055509	HCPEpiC	choroid plexus:	n/a
3	chr7:15055459-15055509	BE2_C	brain:	n/a
4	chr7:15055459-15055509	ProgFib	skin:	n/a
5	chr7:15055459-15055509	AG10803	skin:	n/a
6	chr7:15055459-15055509	HMEC	breast:	n/a
7	chr7:15055459-15055509	IMR90	lung:	fetal
8	chr7:15055459-15055509	GM06990	blood:	n/a
9	chr7:15055459-15055509	HL-60	blood:	n/a
10	chr7:15055459-15055509	A549	lung:	n/a
11	chr7:15055459-15055509	SK-N-SH	brain:	n/a
12	chr7:15055459-15055509	AG09319	gingival:	n/a
13	chr7:15055459-15055509	SK-N-MC	brain:	n/a
14	chr7:15055459-15055509	AG04450	lung:	fetal
15	chr7:15055459-15055509	NHDF-neo	bronchial:	n/a
16	chr7:15055459-15055509	RPTEC	kidney:	n/a
17	chr7:15055459-15055509	HCM	heart:	n/a
18	chr7:15055459-15055509	T-47D	breast:	n/a
19	chr7:15055459-15055509	HepG2	liver:	n/a
20	chr7:15055459-15055509	HNPCEpiC	eye:	n/a
21	chr7:15055459-15055509	HEEpiC	esophagus:	n/a
22	chr7:15055459-15055509	Hela-S3	cervix:	n/a
23	chr7:15055459-15055509	HCT-116	colon:	n/a
24	chr7:15055459-15055509	GM12891	blood:	n/a
25	chr7:15055459-15055509	GM12892	blood:	n/a
26	chr7:15055459-15055509	NB4	blood:	n/a
27	chr7:15055459-15055509	ovcar-3	ovarian:	n/a
28	chr7:15055459-15055509	CMK	blood:	n/a
29	chr7:15055459-15055509	SKMC	muscle:	n/a
30	chr7:15055459-15055509	ECC-1	luminal epithelium:	n/a
31	chr7:15055459-15055509	NT2-D1	testis:	n/a
32	chr7:15055459-15055509	HAEpiC	amniotic membrane:	n/a
33	chr7:15055459-15055509	HIPEpiC	eye:	n/a
34	chr7:15055459-15055509	LNCaP	prostate:	n/a
35	chr7:15055459-15055509	AoSMC	blood vessel:	n/a
36	chr7:15055459-15055509	SAEC	small airway:	n/a
37	chr7:15055459-15055509	PFSK-1	brain:	n/a
38	chr7:15055459-15055509	HCF	heart:	n/a
39	chr7:15055459-15055509	MCF10A-Er-Src	breast:	n/a
40	chr7:15055459-15055509	SK-N-SH_RA	brain:	n/a
41	chr7:15055459-15055509	Jurkat	blood:	n/a
42	chr7:15055459-15055509	HRE	kidney:	n/a
43	chr7:15055459-15055509	HEK293	kidney:	embryo
44	chr7:15055459-15055509	GM12878	blood:	n/a
45	chr7:15055459-15055509	U87	brain:	n/a
46	chr7:15055459-15055509	Hepatocyte	liver:	n/a
47	chr7:15055459-15055509	HUVEC	blood vessel:	n/a
48	chr7:15055459-15055509	HRPEpiC	eye:	n/a
49	chr7:15055459-15055509	HPAEpiC	pulmonary alveolar:	n/a
50	chr7:15055459-15055509	NH-A	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:14737644..14738448-chr7:15055761..15056392,2	MCF-7	breast:
2	chr7:13317591..13319993-chr7:15056107..15057980,2	K562	blood:
3	chr7:15046835..15047773-chr7:15055487..15056275,2	MCF-7	breast:
4	chr7:14756304..14757028-chr7:15055834..15056611,2	MCF-7	breast:
5	chr7:15058053..15060763-chr7:15070842..15072885,2	K562	blood:
6	chr7:14757467..14758291-chr7:15055705..15056411,2	MCF-7	breast:
7	chr7:14757081..14758001-chr7:15054605..15056087,5	MCF-7	breast:
8	chr7:15058053..15060763-chr7:15070842..15072885,2	K562	blood:

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-AC006035.2-4	chr7:15105832-15106137	XLOC_005990

Variant related genes	Relation type
ENSG00000227489	TF binding region
ENSG00000227489	CpG island

Extended variants
information (count: 2726 )
Associated
traits (count: 81 )

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	rs10807778	chr7:15054190-15054191	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs555290930	chr7:15054203-15054204	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs182219176	chr7:15054205-15054206	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs186910345	chr7:15054213-15054214	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs10238625	chr7:15054232-15054233	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
6	rs12113450	chr7:15054255-15054256	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs190175586	chr7:15054271-15054272	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs183155375	chr7:15054360-15054361	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs527654446	chr7:15054364-15054365	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs10264723	chr7:15054370-15054371	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs10249299	chr7:15054391-15054392	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs74750606	chr7:15054418-15054419	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs188574103	chr7:15054438-15054439	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs10264840	chr7:15054444-15054445	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs148734986	chr7:15054452-15054453	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs570925622	chr7:15054470-15054471	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs533557662	chr7:15054479-15054480	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs550036460	chr7:15054490-15054491	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs188044362	chr7:15054492-15054493	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs72576329	chr7:15054494-15054495	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs59798226	chr7:15054512-15054513	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs192997247	chr7:15054579-15054580	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs535498392	chr7:15054605-15054606	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs200896680	chr7:15054615-15054616	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs17168601	chr7:15054623-15054624	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs565641231	chr7:15054644-15054645	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs563704742	chr7:15054697-15054698	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs185653339	chr7:15054701-15054702	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs7793132	chr7:15054756-15054757	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs557948409	chr7:15054786-15054787	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs7793046	chr7:15054804-15054805	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs10643202	chr7:15054828-15054829	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs368257384	chr7:15054829-15054830	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs397978259	chr7:15054833-15054834	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs200489403	chr7:15054834-15054835	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs537227193	chr7:15054841-15054842	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs147594496	chr7:15054861-15054862	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs143031168	chr7:15054862-15054863	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs116722520	chr7:15054870-15054871	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs398111088	chr7:15054872-15054873	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs573769531	chr7:15054874-15054875	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs542651420	chr7:15054905-15054906	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs2358159	chr7:15054908-15054909	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs6980437	chr7:15054916-15054917	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs2215381	chr7:15054935-15054936	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs564781845	chr7:15054949-15054950	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs77646272	chr7:15054962-15054963	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs550341533	chr7:15054970-15054971	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs563453020	chr7:15054986-15054987	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs147505116	chr7:15054997-15054998	Weak transcription Enhancers	n/a	n/a	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:276 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:15047600-15055000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr7:15049600-15055000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr7:15051200-15054800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
4	chr7:15051600-15054400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
5	chr7:15051600-15054800	Weak transcription	HUES64 Cell Line	embryonic stem cell
6	chr7:15051600-15054800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
7	chr7:15051600-15055000	Weak transcription	HUES48 Cell Line	embryonic stem cell
8	chr7:15051800-15055000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
9	chr7:15051800-15055000	Weak transcription	HUES6 Cell Line	embryonic stem cell
10	chr7:15052000-15055000	Weak transcription	H9 Cell Line	embryonic stem cell
11	chr7:15052200-15054200	Weak transcription	Skeletal Muscle Male	skeletal muscle
12	chr7:15052200-15055000	Weak transcription	Skeletal Muscle Female	skeletal muscle
13	chr7:15052200-15055200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr7:15052200-15055200	Weak transcription	Right Ventricle	heart
15	chr7:15052800-15055000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr7:15054000-15054200	Enhancers	Psoas Muscle	Psoas
17	chr7:15054200-15054400	Enhancers	Skeletal Muscle Male	skeletal muscle
18	chr7:15054400-15054800	Weak transcription	Skeletal Muscle Male	skeletal muscle
19	chr7:15054400-15055000	Enhancers	iPS-15b Cell Line	embryonic stem cell
20	chr7:15054800-15055000	Enhancers	HUES64 Cell Line	embryonic stem cell
21	chr7:15054800-15055000	Enhancers	iPS-18 Cell Line	embryonic stem cell
22	chr7:15054800-15055000	Enhancers	iPS-20b Cell Line	embryonic stem cell
23	chr7:15054800-15055200	Enhancers	Skeletal Muscle Male	skeletal muscle
24	chr7:15055000-15055200	Flanking Active TSS	H1 Cell Line	embryonic stem cell
25	chr7:15055000-15055200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
26	chr7:15055000-15055200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr7:15055000-15055200	Flanking Active TSS	H9 Cell Line	embryonic stem cell
28	chr7:15055000-15055200	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
29	chr7:15055000-15055200	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
30	chr7:15055000-15055200	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
31	chr7:15055000-15055200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
32	chr7:15055000-15055200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
33	chr7:15055000-15055200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr7:15055000-15055200	Enhancers	Liver	Liver
35	chr7:15055000-15055200	Enhancers	Brain Germinal Matrix	brain
36	chr7:15055000-15055200	Enhancers	Brain Hippocampus Middle	brain
37	chr7:15055000-15055200	Enhancers	Fetal Brain Female	brain
38	chr7:15055000-15055200	Weak transcription	Left Ventricle	heart
39	chr7:15055000-15055200	Enhancers	Right Atrium	heart
40	chr7:15055000-15055200	Enhancers	Skeletal Muscle Female	skeletal muscle
41	chr7:15055000-15055200	Enhancers	Hela-S3	cervix
42	chr7:15055000-15055200	Enhancers	HMEC	breast
43	chr7:15055000-15055200	Enhancers	NHEK	skin
44	chr7:15055000-15055400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
45	chr7:15055000-15055400	Enhancers	Cortex derived primary cultured neurospheres	brain
46	chr7:15055000-15055400	Enhancers	Fetal Intestine Large	intestine
47	chr7:15055000-15055400	Enhancers	Fetal Intestine Small	intestine
48	chr7:15055000-15055600	Active TSS	ES-I3 Cell Line	embryonic stem cell
49	chr7:15055000-15055600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr7:15055000-15055800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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