Variant report

Variant	nsv1015919
Chromosome Location	chr7:13873800-13908250
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	chr7:13889765-13890070	K562	blood:	n/a	n/a
2	ATF1	chr7:13889729-13890161	K562	blood:	n/a	n/a
3	ATF1	chr7:13900658-13900844	K562	blood:	n/a	n/a
4	ATF3	chr7:13889705-13890029	K562	blood:	n/a	n/a
5	BACH1	chr7:13889847-13890003	H1-hESC	embryonic stem cell:	n/a	chr7:13889889-13889903
6	BACH1	chr7:13873923-13874075	H1-hESC	embryonic stem cell:	n/a	n/a
7	BHLHE40	chr7:13889782-13890158	K562	blood:	n/a	n/a
8	CBX3	chr7:13889630-13890509	HCT-116	colon:	n/a	n/a
9	CBX3	chr7:13889637-13890195	K562	blood:	n/a	n/a
10	CBX3	chr7:13889755-13890146	K562	blood:	n/a	n/a
11	CBX3	chr7:13889571-13890520	HCT-116	colon:	n/a	n/a
12	CCNT2	chr7:13889753-13890143	K562	blood:	n/a	n/a
13	CEBPB	chr7:13880948-13881315	HepG2	liver:	n/a	chr7:13881124-13881135
14	CEBPB	chr7:13900159-13900379	HepG2	liver:	n/a	chr7:13900271-13900282 chr7:13900271-13900284 chr7:13900271-13900284
15	CEBPB	chr7:13886123-13886339	K562	blood:	n/a	n/a
16	CEBPB	chr7:13900168-13900410	H1-hESC	embryonic stem cell:	n/a	chr7:13900271-13900282 chr7:13900271-13900284 chr7:13900271-13900284
17	CEBPB	chr7:13900136-13900404	K562	blood:	n/a	chr7:13900271-13900282 chr7:13900271-13900284 chr7:13900271-13900284
18	CEBPB	chr7:13886138-13886375	A549	lung:	n/a	n/a
19	CEBPB	chr7:13889794-13890080	K562	blood:	n/a	n/a
20	CEBPB	chr7:13880963-13881277	IMR90	lung:	n/a	chr7:13881124-13881135
21	CEBPB	chr7:13886140-13886336	HepG2	liver:	n/a	n/a
22	CEBPB	chr7:13881008-13881269	K562	blood:	n/a	chr7:13881124-13881135
23	CEBPB	chr7:13900060-13900418	A549	lung:	n/a	chr7:13900271-13900282 chr7:13900271-13900284 chr7:13900271-13900284
24	CEBPB	chr7:13891431-13891773	IMR90	lung:	n/a	n/a
25	CEBPB	chr7:13900625-13900913	A549	lung:	n/a	n/a
26	CEBPB	chr7:13886155-13886335	H1-hESC	embryonic stem cell:	n/a	n/a
27	CEBPB	chr7:13880992-13881274	H1-hESC	embryonic stem cell:	n/a	chr7:13881124-13881135
28	CEBPB	chr7:13903094-13903302	H1-hESC	embryonic stem cell:	n/a	n/a
29	CEBPB	chr7:13899934-13900452	IMR90	lung:	n/a	chr7:13900271-13900282 chr7:13900271-13900284 chr7:13900271-13900284
30	CEBPB	chr7:13903039-13903324	K562	blood:	n/a	n/a
31	CEBPB	chr7:13886050-13886429	IMR90	lung:	n/a	n/a
32	CEBPB	chr7:13889742-13890398	IMR90	lung:	n/a	n/a
33	CEBPB	chr7:13903095-13903310	IMR90	lung:	n/a	n/a
34	CEBPB	chr7:13880970-13881205	A549	lung:	n/a	chr7:13881124-13881135
35	CHD2	chr7:13873933-13874094	H1-hESC	embryonic stem cell:	n/a	n/a
36	CTCF	chr7:13902980-13903270	BE2_C	brain:	n/a	chr7:13903159-13903172 chr7:13903146-13903164 chr7:13903149-13903162
37	CTCF	chr7:13902960-13903254	H1-hESC	embryonic stem cell:	n/a	chr7:13903159-13903172 chr7:13903146-13903164 chr7:13903149-13903162
38	CTCF	chr7:13903120-13903270	Caco-2	colon:	n/a	chr7:13903159-13903172 chr7:13903146-13903164 chr7:13903149-13903162
39	CTCF	chr7:13903140-13903290	HPAF	blood vessel:	n/a	chr7:13903159-13903172 chr7:13903146-13903164 chr7:13903149-13903162
40	CTCF	chr7:13903100-13903250	BJ	skin:	n/a	chr7:13903159-13903172 chr7:13903146-13903164 chr7:13903149-13903162
41	CTCF	chr7:13903080-13903230	AG10803	skin:	n/a	chr7:13903159-13903172 chr7:13903146-13903164 chr7:13903149-13903162
42	CTCF	chr7:13903098-13903201	Hela-S3	cervix:	n/a	chr7:13903159-13903172 chr7:13903146-13903164 chr7:13903149-13903162
43	CTCF	chr7:13903060-13903210	HFF-Myc	foreskin:	n/a	chr7:13903159-13903172 chr7:13903146-13903164 chr7:13903149-13903162
44	CTCF	chr7:13903060-13903210	HUVEC	blood vessel:	n/a	chr7:13903159-13903172 chr7:13903146-13903164 chr7:13903149-13903162
45	CTCF	chr7:13902987-13903317	K562	blood:	n/a	chr7:13903159-13903172 chr7:13903146-13903164 chr7:13903149-13903162
46	CTCF	chr7:13903080-13903230	HRPEpiC	eye:	n/a	chr7:13903159-13903172 chr7:13903146-13903164 chr7:13903149-13903162
47	CTCF	chr7:13903080-13903230	K562	blood:	n/a	chr7:13903159-13903172 chr7:13903146-13903164 chr7:13903149-13903162
48	CTCF	chr7:13902960-13903110	HVMF	connective:	n/a	n/a
49	CTCF	chr7:13904410-13904507	K562	blood:	n/a	chr7:13904451-13904472 chr7:13904449-13904467
50	CTCF	chr7:13904340-13904490	HMF	breast:	n/a	chr7:13904451-13904472 chr7:13904449-13904467

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:13889871-13889921	SKMC	muscle:	n/a
2	chr7:13889871-13889921	AoSMC	blood vessel:	n/a
3	chr7:13889871-13889921	HAEpiC	amniotic membrane:	n/a
4	chr7:13889871-13889921	CMK	blood:	n/a
5	chr7:13889871-13889921	HRPEpiC	eye:	n/a
6	chr7:13889871-13889921	AG04450	lung:	fetal
7	chr7:13889871-13889921	NB4	blood:	n/a
8	chr7:13889871-13889921	GM12878	blood:	n/a
9	chr7:13889871-13889921	NHDF-neo	bronchial:	n/a
10	chr7:13889871-13889921	HCPEpiC	choroid plexus:	n/a
11	chr7:13889871-13889921	NHBE	bronchial:	n/a
12	chr7:13889871-13889921	U87	brain:	n/a
13	chr7:13889871-13889921	GM06990	blood:	n/a
14	chr7:13889871-13889921	AG04449	skin:	fetal
15	chr7:13889871-13889921	HNPCEpiC	eye:	n/a
16	chr7:13889871-13889921	GM12891	blood:	n/a
17	chr7:13889871-13889921	SK-N-SH	brain:	n/a
18	chr7:13889871-13889921	HRE	kidney:	n/a
19	chr7:13889871-13889921	PANC-1	pancreas:	n/a
20	chr7:13889871-13889921	HMEC	breast:	n/a
21	chr7:13889871-13889921	HRCEpiC	kidney:	n/a
22	chr7:13889871-13889921	SK-N-SH_RA	brain:	n/a
23	chr7:13889871-13889921	T-47D	breast:	n/a
24	chr7:13889871-13889921	K562	blood:	n/a
25	chr7:13889871-13889921	GM19239	blood:	n/a
26	chr7:13889871-13889921	HPAEpiC	pulmonary alveolar:	n/a
27	chr7:13889871-13889921	AG09309	skin:	n/a
28	chr7:13889871-13889921	A549	lung:	n/a
29	chr7:13889871-13889921	HEK293	kidney:	embryo
30	chr7:13889871-13889921	HUVEC	blood vessel:	n/a
31	chr7:13889871-13889921	NH-A	brain:	n/a
32	chr7:13889871-13889921	HepG2	liver:	n/a
33	chr7:13889871-13889921	HIPEpiC	eye:	n/a
34	chr7:13889871-13889921	Jurkat	blood:	n/a
35	chr7:13889871-13889921	GM12892	blood:	n/a
36	chr7:13889871-13889921	Caco-2	colon:	n/a
37	chr7:13889871-13889921	HL-60	blood:	n/a
38	chr7:13889871-13889921	AG10803	skin:	n/a
39	chr7:13889871-13889921	SK-N-MC	brain:	n/a
40	chr7:13889871-13889921	NT2-D1	testis:	n/a
41	chr7:13889871-13889921	IMR90	lung:	fetal
42	chr7:13889871-13889921	HCF	heart:	n/a
43	chr7:13889871-13889921	H1-hESC	embryonic stem cell:	embryo
44	chr7:13889871-13889921	ECC-1	luminal epithelium:	n/a
45	chr7:13889871-13889921	Hepatocyte	liver:	n/a
46	chr7:13889871-13889921	HEEpiC	esophagus:	n/a
47	chr7:13889871-13889921	ovcar-3	ovarian:	n/a
48	chr7:13889871-13889921	LNCaP	prostate:	n/a
49	chr7:13889871-13889921	HCM	heart:	n/a
50	chr7:13889871-13889921	AG09319	gingival:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:13883716..13885561-chr7:13890341..13892357,2	K562	blood:
2	chr7:13869026..13872125-chr7:13876719..13879737,3	K562	blood:
3	chr7:13898559..13901034-chr7:13906643..13908176,2	K562	blood:
4	chr7:13883716..13885561-chr7:13890341..13892357,2	K562	blood:
5	chr7:13882109..13884330-chr7:14031307..14033942,2	K562	blood:
6	chr7:13887425..13891202-chr7:13891537..13895717,6	K562	blood:
7	chr7:13894294..13896373-chr7:13930641..13933578,2	K562	blood:
8	chr7:13888536..13892464-chr7:13896702..13899784,3	K562	blood:
9	chr7:13888923..13892464-chr7:13896702..13899775,3	K562	blood:
10	chr7:13887425..13891202-chr7:13891537..13895717,6	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ETV1-1	chr7:13898560-13898650	XLOC_006359
2	lnc-ETV1-1	chr7:13893980-13894247	XLOC_006359

Variant related genes	Relation type
ENSG00000224330	TF binding region
ENSG00000213875	TF binding region
ENSG00000224330	CpG island
ENSG00000213875	CpG island
ENSG00000224330	chromatin interactions

Extended variants
information (count: 1397 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:1397 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs143125825	chr7:13873884-13873885	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs189687160	chr7:13873901-13873902	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs182075873	chr7:13873902-13873903	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs556894333	chr7:13873904-13873905	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs73271543	chr7:13873992-13873993	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs147501756	chr7:13874005-13874006	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs12532692	chr7:13874028-13874029	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs188794013	chr7:13874074-13874075	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs561822744	chr7:13874086-13874087	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs538784337	chr7:13874091-13874092	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs148134218	chr7:13874133-13874134	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs193226034	chr7:13874166-13874167	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs578192799	chr7:13874169-13874170	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs527787005	chr7:13874195-13874196	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs544058022	chr7:13874208-13874209	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs17677337	chr7:13874245-13874246	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs183499933	chr7:13874261-13874262	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs549143857	chr7:13874274-13874275	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs34745585	chr7:13874296-13874297	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs559489491	chr7:13874300-13874301	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs141965192	chr7:13874320-13874321	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs570944970	chr7:13874337-13874338	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs551408162	chr7:13874348-13874349	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs571189241	chr7:13874349-13874350	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs188596278	chr7:13874369-13874370	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs150690826	chr7:13874391-13874392	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs567384483	chr7:13874434-13874435	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs536028844	chr7:13874454-13874455	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs140037777	chr7:13874505-13874506	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs535736276	chr7:13874507-13874508	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs572210004	chr7:13874621-13874622	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs534753261	chr7:13874641-13874642	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs12699563	chr7:13874690-13874691	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
34	rs143957332	chr7:13874705-13874706	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs368977656	chr7:13874707-13874708	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs192760638	chr7:13874773-13874774	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs184153734	chr7:13874776-13874777	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs145942964	chr7:13874790-13874791	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs76121984	chr7:13874848-13874849	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs559948430	chr7:13874866-13874867	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs202086044	chr7:13874871-13874872	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs76780124	chr7:13874873-13874874	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs186945923	chr7:13874879-13874880	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs564756284	chr7:13874898-13874899	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs530510586	chr7:13874925-13874926	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs576508510	chr7:13874930-13874931	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs550641406	chr7:13874969-13874970	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs567548529	chr7:13874970-13874971	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs2108151	chr7:13874978-13874979	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs143295100	chr7:13874985-13874986	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:89)

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
Renal cell carcinoma	18194544	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
Pancreatic ductal adenocarcinoma	19077451	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Bipolar disorder	19114987	CNVD
Breast cancer	22522925	CNVD
Prostate cancer	21298110	CNVD
Glioblastoma multiforme	22122801	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Prostate cancer	17079440	CNVD

Chromatin state (count:268 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:13870200-13873800	Weak transcription	HSMM	muscle
2	chr7:13870400-13873800	Weak transcription	Fetal Muscle Leg	muscle
3	chr7:13870400-13874000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr7:13870800-13873800	Weak transcription	Osteobl	bone
5	chr7:13872200-13873800	Weak transcription	Muscle Satellite Cultured Cells	--
6	chr7:13872200-13874000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr7:13873000-13874200	Enhancers	Fetal Brain Male	brain
8	chr7:13873000-13874400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
9	chr7:13873000-13875200	Enhancers	H1 Cell Line	embryonic stem cell
10	chr7:13873200-13876000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr7:13873200-13876600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr7:13873200-13877000	Enhancers	iPS-18 Cell Line	embryonic stem cell
13	chr7:13873400-13874800	Enhancers	iPS-20b Cell Line	embryonic stem cell
14	chr7:13873400-13875400	Enhancers	Breast Myoepithelial Primary Cells	Breast
15	chr7:13873400-13875400	Enhancers	Fetal Heart	heart
16	chr7:13873400-13875600	Enhancers	iPS-15b Cell Line	embryonic stem cell
17	chr7:13873400-13877400	Enhancers	HUES64 Cell Line	embryonic stem cell
18	chr7:13873600-13874000	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
19	chr7:13873600-13874000	Enhancers	Skeletal Muscle Female	skeletal muscle
20	chr7:13873600-13874400	Enhancers	Fetal Lung	lung
21	chr7:13873600-13875400	Enhancers	HSMMtube	muscle
22	chr7:13873600-13875600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
23	chr7:13873600-13876000	Weak transcription	Pancreatic Islets	Pancreatic Islet
24	chr7:13873600-13876600	Enhancers	Cortex derived primary cultured neurospheres	brain
25	chr7:13873600-13877000	Enhancers	ES-I3 Cell Line	embryonic stem cell
26	chr7:13873800-13874000	Enhancers	Psoas Muscle	Psoas
27	chr7:13873800-13874000	Active TSS	Stomach Smooth Muscle	stomach
28	chr7:13873800-13874200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr7:13873800-13874200	Enhancers	Fetal Muscle Leg	muscle
30	chr7:13873800-13874200	Enhancers	Skeletal Muscle Male	skeletal muscle
31	chr7:13873800-13874200	Enhancers	Osteobl	bone
32	chr7:13873800-13874400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr7:13873800-13874400	Enhancers	HSMM	muscle
34	chr7:13873800-13874600	Enhancers	NHEK	skin
35	chr7:13873800-13875600	Enhancers	HUES6 Cell Line	embryonic stem cell
36	chr7:13874000-13874200	Enhancers	Muscle Satellite Cultured Cells	--
37	chr7:13874000-13874200	Flanking Active TSS	Stomach Smooth Muscle	stomach
38	chr7:13874000-13874400	Flanking Active TSS	Psoas Muscle	Psoas
39	chr7:13874000-13874400	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
40	chr7:13874000-13874600	Enhancers	HUES48 Cell Line	embryonic stem cell
41	chr7:13874000-13875000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr7:13874000-13875400	Enhancers	Fetal Brain Female	brain
43	chr7:13874000-13876400	Enhancers	H9 Cell Line	embryonic stem cell
44	chr7:13874000-13876400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
45	chr7:13874000-13876600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
46	chr7:13874200-13875200	Weak transcription	Fetal Muscle Leg	muscle
47	chr7:13874400-13874800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
48	chr7:13874600-13875000	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
49	chr7:13874800-13875600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
50	chr7:13874800-13876000	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell

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