Variant report

Variant	nsv520726
Chromosome Location	chr1:57143986-57205666
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:492)
CpG islands
(count:61)
Chromatin interactive
region (count:11)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:4)

(count:492 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:57174889-57175345	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:57175004-57175318	K562	blood:	n/a	n/a
3	ARID3A	chr1:57154114-57154744	HepG2	liver:	n/a	n/a
4	ATF3	chr1:57154051-57154748	A549	lung:	n/a	n/a
5	ATF3	chr1:57154017-57154634	A549	lung:	n/a	n/a
6	BACH1	chr1:57154125-57154689	H1-hESC	embryonic stem cell:	n/a	n/a
7	BATF	chr1:57154126-57154420	GM12878	blood:	n/a	n/a
8	BATF	chr1:57154153-57154386	GM12878	blood:	n/a	n/a
9	BCL3	chr1:57154014-57154765	A549	lung:	n/a	n/a
10	BCL3	chr1:57153922-57154813	A549	lung:	n/a	chr1:57153958-57153967
11	BRCA1	chr1:57154096-57154771	Hela-S3	cervix:	n/a	n/a
12	CBX3	chr1:57154079-57154839	HCT-116	colon:	n/a	n/a
13	CBX3	chr1:57154039-57154860	HCT-116	colon:	n/a	n/a
14	CEBPB	chr1:57151760-57152189	Hela-S3	cervix:	n/a	chr1:57151956-57151967
15	CEBPB	chr1:57154073-57154867	HCT-116	colon:	n/a	n/a
16	CEBPB	chr1:57185718-57186012	IMR90	lung:	n/a	chr1:57185816-57185829
17	CEBPB	chr1:57185748-57186010	HepG2	liver:	n/a	chr1:57185816-57185829
18	CEBPB	chr1:57154256-57154687	A549	lung:	n/a	n/a
19	CEBPB	chr1:57153879-57154893	HCT-116	colon:	n/a	n/a
20	CEBPB	chr1:57154130-57154736	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr1:57185747-57185997	A549	lung:	n/a	chr1:57185816-57185829
22	CEBPB	chr1:57154082-57154851	A549	lung:	n/a	n/a
23	CEBPB	chr1:57151796-57152150	IMR90	lung:	n/a	chr1:57151956-57151967
24	CHD2	chr1:57154128-57154778	Hela-S3	cervix:	n/a	n/a
25	CREB1	chr1:57154203-57154454	A549	lung:	n/a	n/a
26	CTCF	chr1:57175100-57175250	HPAF	blood vessel:	n/a	n/a
27	CTCF	chr1:57175040-57175190	Caco-2	colon:	n/a	n/a
28	CTCF	chr1:57174840-57174990	HA-sp	spinal cord:	n/a	n/a
29	CTCF	chr1:57175060-57175210	GM12878	blood:	n/a	n/a
30	CTCF	chr1:57175040-57175190	NHEK	skin:	n/a	n/a
31	CTCF	chr1:57175084-57175254	LNCaP	prostate:	n/a	n/a
32	CTCF	chr1:57175053-57175276	GM10248	blood:	n/a	n/a
33	CTCF	chr1:57175620-57175770	AoAF	blood vessel:	n/a	n/a
34	CTCF	chr1:57175045-57175282	GM12878	blood:	n/a	n/a
35	CTCF	chr1:57174953-57175287	A549	lung:	n/a	n/a
36	CTCF	chr1:57175160-57175310	WI-38	lung:	n/a	n/a
37	CTCF	chr1:57175140-57175290	GM12878	blood:	n/a	n/a
38	CTCF	chr1:57175060-57175210	GM12873	blood:	n/a	n/a
39	CTCF	chr1:57175100-57175250	Hela-S3	cervix:	n/a	n/a
40	CTCF	chr1:57175060-57175210	HCT-116	colon:	n/a	n/a
41	CTCF	chr1:57175740-57175890	HPF	lung:	n/a	n/a
42	CTCF	chr1:57175060-57175246	GM10266	blood:	n/a	n/a
43	CTCF	chr1:57175140-57175290	GM12872	blood:	n/a	n/a
44	CTCF	chr1:57175100-57175250	GM12872	blood:	n/a	n/a
45	CTCF	chr1:57175060-57175210	HBMEC	blood vessel:	n/a	n/a
46	CTCF	chr1:57175080-57175230	HL-60	blood:	n/a	n/a
47	CTCF	chr1:57175080-57175230	AG04449	skin:	n/a	n/a
48	CTCF	chr1:57175048-57175253	Pancreas_OC	pancreas:	n/a	n/a
49	CTCF	chr1:57175960-57176110	NHLF	lung:	n/a	n/a
50	CTCF	chr1:57152220-57152370	NHEK	skin:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:57176315-57176365	HPAEpiC	pulmonary alveolar:	n/a
2	chr1:57176315-57176365	U87	brain:	n/a
3	chr1:57176315-57176365	SKMC	muscle:	n/a
4	chr1:57176315-57176365	CMK	blood:	n/a
5	chr1:57176315-57176365	HRE	kidney:	n/a
6	chr1:57176315-57176365	GM12878	blood:	n/a
7	chr1:57176315-57176365	PrEC	prostate:	n/a
8	chr1:57176315-57176365	LNCaP	prostate:	n/a
9	chr1:57176315-57176365	AG04449	skin:	fetal
10	chr1:57176315-57176365	HNPCEpiC	eye:	n/a
11	chr1:57176315-57176365	SK-N-SH	brain:	n/a
12	chr1:57176315-57176365	HCM	heart:	n/a
13	chr1:57176315-57176365	GM12892	blood:	n/a
14	chr1:57176315-57176365	NHBE	bronchial:	n/a
15	chr1:57176315-57176365	T-47D	breast:	n/a
16	chr1:57176315-57176365	Caco-2	colon:	n/a
17	chr1:57176315-57176365	HepG2	liver:	n/a
18	chr1:57176315-57176365	NH-A	brain:	n/a
19	chr1:57176315-57176365	SK-N-MC	brain:	n/a
20	chr1:57176315-57176365	ovcar-3	ovarian:	n/a
21	chr1:57176315-57176365	SAEC	small airway:	n/a
22	chr1:57176315-57176365	HIPEpiC	eye:	n/a
23	chr1:57176315-57176365	HRCEpiC	kidney:	n/a
24	chr1:57176315-57176365	HCT-116	colon:	n/a
25	chr1:57176315-57176365	PFSK-1	brain:	n/a
26	chr1:57176315-57176365	A549	lung:	n/a
27	chr1:57176315-57176365	GM19239	blood:	n/a
28	chr1:57176315-57176365	HUVEC	blood vessel:	n/a
29	chr1:57176315-57176365	HRPEpiC	eye:	n/a
30	chr1:57176315-57176365	MCF-7	breast:	n/a
31	chr1:57176315-57176365	RPTEC	kidney:	n/a
32	chr1:57176315-57176365	HEK293	kidney:	embryo
33	chr1:57176315-57176365	MCF10A-Er-Src	breast:	n/a
34	chr1:57176315-57176365	GM12891	blood:	n/a
35	chr1:57176315-57176365	BJ	skin:	n/a
36	chr1:57176315-57176365	PANC-1	pancreas:	n/a
37	chr1:57176315-57176365	AoSMC	blood vessel:	n/a
38	chr1:57176315-57176365	HL-60	blood:	n/a
39	chr1:57176315-57176365	GM06990	blood:	n/a
40	chr1:57176315-57176365	BE2_C	brain:	n/a
41	chr1:57176315-57176365	AG04450	lung:	fetal
42	chr1:57176315-57176365	HCPEpiC	choroid plexus:	n/a
43	chr1:57176315-57176365	ECC-1	luminal epithelium:	n/a
44	chr1:57176315-57176365	HMEC	breast:	n/a
45	chr1:57176315-57176365	H1-hESC	embryonic stem cell:	embryo
46	chr1:57176315-57176365	HEEpiC	esophagus:	n/a
47	chr1:57176315-57176365	K562	blood:	n/a
48	chr1:57176315-57176365	NB4	blood:	n/a
49	chr1:57176315-57176365	ProgFib	skin:	n/a
50	chr1:57176315-57176365	AG10803	skin:	n/a

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:57174557..57176928-chr1:57179805..57181791,3	K562	blood:
2	chr1:55750589..55751527-chr1:57174232..57175597,4	K562	blood:
3	chr1:56874466..56875023-chr1:57174644..57175624,2	K562	blood:
4	chr1:57131079..57133360-chr1:57142832..57145132,2	MCF-7	breast:
5	chr1:57183853..57186266-chr1:57187867..57189916,2	K562	blood:
6	chr1:57183853..57186266-chr1:57187867..57189916,2	K562	blood:
7	chr1:55923553..55925423-chr1:57168281..57171195,2	MCF-7	breast:
8	chr1:57174557..57176928-chr1:57179805..57181791,3	K562	blood:
9	chr1:57188830..57190697-chr1:57194893..57196502,2	K562	blood:
10	chr1:57184766..57187381-chr1:57187867..57189921,2	K562	blood:
11	chr1:57188830..57190697-chr1:57194893..57196502,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PPAP2B-6	chr1:57192221-57192256	NONHSAT003459
2	lnc-PPAP2B-6	chr1:57202760-57203320	NONHSAT003459
3	lnc-PRKAA2-8	chr1:57179323-57181008	NONHSAT003458

No data

(count:4 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	PRKAA2	hsa-miR-98-5p	chr1:57180003-57180010
2	PRKAA2	hsa-let-7b-5p	chr1:57180003-57180010
3	PRKAA2	hsa-miR-182-5p	chr1:57174866-57174873
4	C1orf168	hsa-miR-148b-3p	chr1:57184510-57184531

Variant related genes	Relation type
C1orf168	TF binding region
C1orf168	CpG island
ENSG00000187889	chromatin interactions

Extended variants
information (count: 2253 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:2253 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2796498	chr1:57143986-57143987	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs568724605	chr1:57143993-57143994	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs34203879	chr1:57144043-57144044	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs533902190	chr1:57144049-57144050	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs553093012	chr1:57144066-57144067	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs573148373	chr1:57144099-57144100	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs545184572	chr1:57144104-57144105	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs116677022	chr1:57144118-57144119	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs575311825	chr1:57144173-57144174	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs544436767	chr1:57144257-57144258	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs561137040	chr1:57144286-57144287	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs115890455	chr1:57144288-57144289	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs540882053	chr1:57144319-57144320	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs12116641	chr1:57144344-57144345	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs144835366	chr1:57144367-57144368	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs546892812	chr1:57144384-57144385	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs567685381	chr1:57144400-57144401	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs559909391	chr1:57144409-57144410	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs12723688	chr1:57144419-57144420	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs2796499	chr1:57144438-57144439	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs551868469	chr1:57144442-57144443	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs569010091	chr1:57144455-57144456	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs186287828	chr1:57144456-57144457	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs375494946	chr1:57144465-57144466	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs568210726	chr1:57144468-57144469	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs6667323	chr1:57144513-57144514	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs35381743	chr1:57144549-57144550	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs534087728	chr1:57144558-57144559	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs137884411	chr1:57144560-57144561	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs566771755	chr1:57144569-57144570	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs539050667	chr1:57144574-57144575	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs558664264	chr1:57144582-57144583	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs556922986	chr1:57144641-57144642	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs537946879	chr1:57144647-57144648	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs191987723	chr1:57144649-57144650	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs574656476	chr1:57144657-57144658	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs540590169	chr1:57144663-57144664	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs560867376	chr1:57144664-57144665	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs577450760	chr1:57144688-57144689	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs142427417	chr1:57144724-57144725	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs184205085	chr1:57144829-57144830	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs369412204	chr1:57144837-57144838	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs556229818	chr1:57144846-57144847	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs112201668	chr1:57144863-57144864	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs548270101	chr1:57144889-57144890	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs561881928	chr1:57144926-57144927	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs575500369	chr1:57144996-57144997	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs376481573	chr1:57144997-57144998	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs187580291	chr1:57145030-57145031	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs527455984	chr1:57145031-57145032	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:95)

Disease	PMID	Source
Papillary thyroid carcinoma	21436994	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Colorectal cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Melanoma	17363583	CNVD
Cancer	21129771	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Meckel-Gruber syndrome	21572526	CNVD
Breast cancer	16620391	CNVD
Multiple myeloma	16616336	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21509527	CNVD
Myelofibrosis	22110671	CNVD
Developmental delay	19490664	CNVD
Glioblastoma multiforme	22286061	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	22522925	CNVD
Congenital anomalies of the kidney and urinary tract	18852474	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:428 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:57122800-57169600	Weak transcription	Ovary	ovary
2	chr1:57125600-57169800	Weak transcription	Aorta	Aorta
3	chr1:57129800-57152200	Weak transcription	Psoas Muscle	Psoas
4	chr1:57135400-57160200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr1:57136200-57161400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
6	chr1:57141600-57144000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
7	chr1:57141600-57144000	Enhancers	Skeletal Muscle Female	skeletal muscle
8	chr1:57141800-57144000	Enhancers	Hela-S3	cervix
9	chr1:57142200-57145000	Weak transcription	Left Ventricle	heart
10	chr1:57142600-57144000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr1:57142600-57145000	Weak transcription	HepG2	liver
12	chr1:57142600-57150400	Weak transcription	Skeletal Muscle Male	skeletal muscle
13	chr1:57143000-57153600	Weak transcription	NH-A	brain
14	chr1:57143400-57149400	Weak transcription	Fetal Heart	heart
15	chr1:57143600-57153600	Weak transcription	HUES64 Cell Line	embryonic stem cell
16	chr1:57144000-57145200	Weak transcription	Skeletal Muscle Female	skeletal muscle
17	chr1:57144000-57148800	Weak transcription	Hela-S3	cervix
18	chr1:57144000-57149200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
19	chr1:57144200-57165000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
20	chr1:57144200-57171800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
21	chr1:57144400-57169400	Weak transcription	Fetal Kidney	kidney
22	chr1:57144400-57173600	Weak transcription	Colon Smooth Muscle	Colon
23	chr1:57145000-57146000	Strong transcription	Left Ventricle	heart
24	chr1:57145000-57146000	Strong transcription	HepG2	liver
25	chr1:57145200-57146000	Strong transcription	Skeletal Muscle Female	skeletal muscle
26	chr1:57146000-57148200	Weak transcription	HepG2	liver
27	chr1:57146000-57149400	Weak transcription	Skeletal Muscle Female	skeletal muscle
28	chr1:57146000-57149600	Weak transcription	Left Ventricle	heart
29	chr1:57148200-57150000	Enhancers	HepG2	liver
30	chr1:57148800-57152600	Enhancers	Hela-S3	cervix
31	chr1:57149200-57150600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
32	chr1:57149400-57149600	Enhancers	Right Ventricle	heart
33	chr1:57149400-57150400	Enhancers	Fetal Heart	heart
34	chr1:57149400-57150600	Enhancers	Skeletal Muscle Female	skeletal muscle
35	chr1:57149600-57150000	Enhancers	Left Ventricle	heart
36	chr1:57149600-57166000	Weak transcription	Right Ventricle	heart
37	chr1:57150000-57151800	Weak transcription	HepG2	liver
38	chr1:57150000-57165800	Weak transcription	Left Ventricle	heart
39	chr1:57150400-57150600	Flanking Active TSS	Fetal Heart	heart
40	chr1:57150400-57151000	Enhancers	Skeletal Muscle Male	skeletal muscle
41	chr1:57150600-57151400	Enhancers	Fetal Heart	heart
42	chr1:57150600-57152000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
43	chr1:57150600-57152000	Weak transcription	Skeletal Muscle Female	skeletal muscle
44	chr1:57150600-57168000	Weak transcription	Stomach Smooth Muscle	stomach
45	chr1:57151000-57165600	Weak transcription	Skeletal Muscle Male	skeletal muscle
46	chr1:57151400-57152200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
47	chr1:57151400-57153600	Enhancers	A549	lung
48	chr1:57151400-57165400	Weak transcription	Fetal Heart	heart
49	chr1:57151800-57152400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr1:57151800-57152400	Enhancers	Muscle Satellite Cultured Cells	--

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