Variant report

Variant	nsv4647
Chromosome Location	chr4:187820591-187855243
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	chr4:187825273-187825725	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:187821710-187822121	K562	blood:	n/a	n/a
3	ARID3A	chr4:187853628-187853802	HepG2	liver:	n/a	n/a
4	ARID3A	chr4:187822170-187822409	HepG2	liver:	n/a	n/a
5	ATF1	chr4:187821710-187821974	K562	blood:	n/a	n/a
6	ATF3	chr4:187821648-187821997	K562	blood:	n/a	n/a
7	BACH1	chr4:187821739-187821994	K562	blood:	n/a	n/a
8	BATF	chr4:187825325-187825626	GM12878	blood:	n/a	n/a
9	BHLHE40	chr4:187821833-187821839	K562	blood:	n/a	n/a
10	BHLHE40	chr4:187831637-187831639	K562	blood:	n/a	n/a
11	CBX3	chr4:187850180-187850774	HCT-116	colon:	n/a	n/a
12	CBX3	chr4:187853152-187854568	HCT-116	colon:	n/a	n/a
13	CBX3	chr4:187848532-187849172	HCT-116	colon:	n/a	n/a
14	CBX3	chr4:187821529-187822040	K562	blood:	n/a	n/a
15	CBX3	chr4:187853176-187854694	HCT-116	colon:	n/a	n/a
16	CEBPB	chr4:187821544-187821995	K562	blood:	n/a	n/a
17	CEBPB	chr4:187825205-187825803	A549	lung:	n/a	chr4:187825335-187825352
18	CEBPB	chr4:187831701-187831789	HepG2	liver:	n/a	chr4:187831756-187831767
19	CEBPB	chr4:187852790-187853007	K562	blood:	n/a	chr4:187852912-187852923 chr4:187852911-187852922
20	CEBPB	chr4:187831604-187831867	MCF-7	breast:	n/a	chr4:187831756-187831767
21	CEBPB	chr4:187831588-187831941	K562	blood:	n/a	chr4:187831756-187831767
22	CEBPB	chr4:187831406-187832021	HCT-116	colon:	n/a	chr4:187831756-187831767
23	CEBPB	chr4:187825309-187825702	A549	lung:	n/a	chr4:187825335-187825352
24	CEBPB	chr4:187821391-187821998	IMR90	lung:	n/a	n/a
25	CEBPB	chr4:187850155-187850790	HCT-116	colon:	n/a	n/a
26	CEBPB	chr4:187825257-187825708	A549	lung:	n/a	chr4:187825335-187825352
27	CEBPB	chr4:187831481-187831998	HCT-116	colon:	n/a	chr4:187831756-187831767
28	CEBPB	chr4:187852609-187855078	HCT-116	colon:	n/a	chr4:187854661-187854674 chr4:187852912-187852923 chr4:187853362-187853379 chr4:187852911-187852922 chr4:187854661-187854672 chr4:187854661-187854674
29	CEBPB	chr4:187852728-187854633	HCT-116	colon:	n/a	chr4:187852912-187852923 chr4:187853362-187853379 chr4:187852911-187852922
30	CEBPB	chr4:187825310-187825703	IMR90	lung:	n/a	chr4:187825335-187825352
31	CEBPB	chr4:187831594-187831886	HepG2	liver:	n/a	chr4:187831756-187831767
32	CEBPB	chr4:187825354-187825618	HepG2	liver:	n/a	n/a
33	CEBPB	chr4:187831585-187831938	Hela-S3	cervix:	n/a	chr4:187831756-187831767
34	CEBPB	chr4:187852834-187853004	HepG2	liver:	n/a	chr4:187852912-187852923 chr4:187852911-187852922
35	CEBPB	chr4:187841693-187842582	IMR90	lung:	n/a	n/a
36	CEBPB	chr4:187825255-187825688	Hela-S3	cervix:	n/a	chr4:187825335-187825352
37	CEBPB	chr4:187852720-187853101	IMR90	lung:	n/a	chr4:187852912-187852923 chr4:187852911-187852922
38	CTCF	chr4:187848920-187849070	HCPEpiC	choroid plexus:	n/a	chr4:187848994-187849002 chr4:187848995-187849003 chr4:187848989-187849002
39	CTCF	chr4:187823211-187823259	NHEK	skin:	n/a	n/a
40	CTCF	chr4:187848940-187849090	HCT-116	colon:	n/a	chr4:187848994-187849002 chr4:187848995-187849003 chr4:187848989-187849002
41	CTCF	chr4:187848820-187848970	NHEK	skin:	n/a	n/a
42	CTCF	chr4:187836163-187836204	Hela-S3	cervix:	n/a	n/a
43	CTCF	chr4:187848920-187849070	HAc	cerebellar:	n/a	chr4:187848994-187849002 chr4:187848995-187849003 chr4:187848989-187849002
44	CTCF	chr4:187826688-187826726	Fibrobl	skin:	n/a	n/a
45	CTCF	chr4:187854020-187854170	AG10803	skin:	n/a	n/a
46	CTCF	chr4:187848917-187848989	HepG2	liver:	n/a	n/a
47	CTCF	chr4:187848997-187849000	HepG2	liver:	n/a	n/a
48	CTCF	chr4:187822120-187822270	HPAF	blood vessel:	n/a	n/a
49	CTCF	chr4:187848940-187849054	H1-hESC	embryonic stem cell:	n/a	chr4:187848994-187849002 chr4:187848995-187849003 chr4:187848989-187849002
50	CTCF	chr4:187848920-187849070	AG04450	lung:	n/a	chr4:187848994-187849002 chr4:187848995-187849003 chr4:187848989-187849002

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:187840611-187840661	HCF	heart:	n/a
2	chr4:187840611-187840661	HCF	heart:	n/a
3	chr4:187851418-187851468	HCPEpiC	choroid plexus:	n/a
4	chr4:187851724-187851774	SAEC	small airway:	n/a
5	chr4:187840611-187840661	NHBE	bronchial:	n/a
6	chr4:187840667-187840717	GM12892	blood:	n/a
7	chr4:187840667-187840717	NT2-D1	testis:	n/a
8	chr4:187840667-187840717	HepG2	liver:	n/a
9	chr4:187851418-187851468	Hepatocyte	liver:	n/a
10	chr4:187840862-187840912	AG10803	skin:	n/a
11	chr4:187840667-187840717	AG10803	skin:	n/a
12	chr4:187840611-187840661	GM19239	blood:	n/a
13	chr4:187840611-187840661	SK-N-SH	brain:	n/a
14	chr4:187840667-187840717	BE2_C	brain:	n/a
15	chr4:187840667-187840717	H1-hESC	embryonic stem cell:	embryo
16	chr4:187851333-187851383	HEEpiC	esophagus:	n/a
17	chr4:187840667-187840717	PANC-1	pancreas:	n/a
18	chr4:187840862-187840912	IMR90	lung:	fetal
19	chr4:187840667-187840717	ECC-1	luminal epithelium:	n/a
20	chr4:187851586-187851636	SAEC	small airway:	n/a
21	chr4:187840862-187840912	AG09309	skin:	n/a
22	chr4:187851333-187851383	NT2-D1	testis:	n/a
23	chr4:187840862-187840912	HCM	heart:	n/a
24	chr4:187851724-187851774	Jurkat	blood:	n/a
25	chr4:187851586-187851636	PrEC	prostate:	n/a
26	chr4:187851405-187851455	SK-N-MC	brain:	n/a
27	chr4:187851418-187851468	SK-N-SH	brain:	n/a
28	chr4:187840667-187840717	HRCEpiC	kidney:	n/a
29	chr4:187840862-187840912	LNCaP	prostate:	n/a
30	chr4:187851418-187851468	HCF	heart:	n/a
31	chr4:187851405-187851455	AoSMC	blood vessel:	n/a
32	chr4:187851724-187851774	U87	brain:	n/a
33	chr4:187840862-187840912	MCF-7	breast:	n/a
34	chr4:187851405-187851455	A549	lung:	n/a
35	chr4:187851333-187851383	PrEC	prostate:	n/a
36	chr4:187840667-187840717	AG04450	lung:	fetal
37	chr4:187840667-187840717	SK-N-MC	brain:	n/a
38	chr4:187851586-187851636	CMK	blood:	n/a
39	chr4:187851586-187851636	AG09319	gingival:	n/a
40	chr4:187840862-187840912	AG04450	lung:	fetal
41	chr4:187851724-187851774	SK-N-SH_RA	brain:	n/a
42	chr4:187840862-187840912	HAEpiC	amniotic membrane:	n/a
43	chr4:187851724-187851774	HIPEpiC	eye:	n/a
44	chr4:187840862-187840912	ovcar-3	ovarian:	n/a
45	chr4:187840862-187840912	BE2_C	brain:	n/a
46	chr4:187851418-187851468	PFSK-1	brain:	n/a
47	chr4:187851418-187851468	NT2-D1	testis:	n/a
48	chr4:187851586-187851636	PANC-1	pancreas:	n/a
49	chr4:187851333-187851383	SAEC	small airway:	n/a
50	chr4:187851586-187851636	HCPEpiC	choroid plexus:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:187702948..187705032-chr4:187853740..187855963,2	K562	blood:
2	chr4:187828658..187830841-chr4:187832726..187835053,2	K562	blood:
3	chr4:187834719..187836677-chr4:187841436..187844057,2	MCF-7	breast:
4	chr4:187838828..187841268-chr4:187853169..187855944,2	K562	blood:
5	chr4:187761346..187763070-chr4:187833747..187836237,2	K562	blood:
6	chr4:187828658..187830841-chr4:187832726..187835053,2	K562	blood:
7	chr4:187749742..187751497-chr4:187825991..187828310,2	K562	blood:
8	chr4:187678770..187680807-chr4:187839575..187841188,2	K562	blood:
9	chr4:187848247..187850848-chr4:187854272..187856829,2	K562	blood:
10	chr4:187834719..187836677-chr4:187841436..187844057,2	MCF-7	breast:
11	chr4:187819733..187822489-chr4:187823913..187825517,2	MCF-7	breast:
12	chr4:187848247..187850848-chr4:187854272..187856829,2	K562	blood:
13	chr4:187838828..187841268-chr4:187853169..187855944,2	K562	blood:
14	chr4:187844136..187846877-chr4:187850742..187852747,2	K562	blood:
15	chr4:187676723..187679624-chr4:187847276..187848972,2	K562	blood:
16	chr4:187844136..187846877-chr4:187850742..187852747,2	K562	blood:
17	chr4:187831408..187833132-chr4:187833213..187835608,2	MCF-7	breast:
18	chr4:187831408..187833132-chr4:187833213..187835608,2	MCF-7	breast:
19	chr4:187646746..187649449-chr4:187824411..187826046,2	MCF-7	breast:
20	chr4:187811417..187813620-chr4:187839984..187841976,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-F11-11	chr4:187821694-187821992	NONHSAT099678

Variant related genes	Relation type
MRPS36P2	TF binding region
MRPS36P2	CpG island
ENSG00000249539	chromatin interactions
ENSG00000250829	chromatin interactions
ENSG00000083857	chromatin interactions

Extended variants
information (count: 1615 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:1615 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs574133307	chr4:187820604-187820605	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs13125414	chr4:187820621-187820622	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs561340953	chr4:187820659-187820660	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs185431389	chr4:187820662-187820663	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs139448979	chr4:187820668-187820669	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs553870345	chr4:187820674-187820675	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs576821104	chr4:187820698-187820699	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs545979531	chr4:187820713-187820714	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs189745551	chr4:187820721-187820722	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs576420059	chr4:187820731-187820732	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs140465261	chr4:187820762-187820763	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs528920139	chr4:187820769-187820770	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs547044654	chr4:187820821-187820822	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs540256712	chr4:187820853-187820854	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs560645117	chr4:187820859-187820860	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs550383919	chr4:187820861-187820862	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs532454958	chr4:187820865-187820866	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs370309631	chr4:187820889-187820890	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs552376222	chr4:187820902-187820903	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs374337875	chr4:187820923-187820924	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs375024192	chr4:187820941-187820942	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs376114100	chr4:187820942-187820943	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs58004318	chr4:187820950-187820951	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs569077507	chr4:187820957-187820958	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs571569139	chr4:187820967-187820968	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs181336739	chr4:187821041-187821042	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs79435946	chr4:187821053-187821054	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs409666	chr4:187821081-187821082	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs532764289	chr4:187821122-187821123	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs551505196	chr4:187821165-187821166	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs578135	chr4:187821208-187821209	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs538985185	chr4:187821209-187821210	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs375974055	chr4:187821211-187821212	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs556277451	chr4:187821237-187821238	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs75234906	chr4:187821253-187821254	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs534067589	chr4:187821271-187821272	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs542042173	chr4:187821274-187821275	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs146567756	chr4:187821317-187821318	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs537302676	chr4:187821325-187821326	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs572207290	chr4:187821328-187821329	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs555732565	chr4:187821385-187821386	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs540625801	chr4:187821403-187821404	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs186326298	chr4:187821404-187821405	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs560260687	chr4:187821446-187821447	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs141035442	chr4:187821490-187821491	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs117873054	chr4:187821540-187821541	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs562623251	chr4:187821544-187821545	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs531834493	chr4:187821554-187821555	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs548331635	chr4:187821569-187821570	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs114347351	chr4:187821584-187821585	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:81)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Oral squamous cell carcinoma	17134496	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	16608533	CNVD
Wilms tumour	21544195	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Breast cancer	16272173	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Olfactory neuroblastoma	18408657	CNVD
Breast cancer	21785460	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	21633010	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20581869	CNVD
Hepatocellular carcinoma	16750200	CNVD
abnormal development	18461090	CNVD
Neuroblastoma	16790693	CNVD
Colorectal cancer	16774939	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Basal cell lymphoma	17053054	CNVD
Facioscapulohumeral muscular dystrophy	21829175	CNVD
Disorders of sex development	21048976	CNVD
Ovarian cancer	20844748	CNVD
Autism	18414403	CNVD
Urothelial carcinoma	21177765	CNVD
Cancer	20164920	CNVD
Cancer	20164919	CNVD
Breast cancer	20409316	CNVD
Rhabdomyosarcoma	16790082	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	21399695	CNVD
Developmental delay	22127048	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Cervical cancer	21063398	CNVD
Oral cancer	21386901	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:398 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:187808200-187821400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr4:187811200-187821400	Weak transcription	K562	blood
3	chr4:187813200-187821200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr4:187816400-187829400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr4:187818800-187821200	Weak transcription	HUVEC	blood vessel
6	chr4:187821200-187822600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr4:187821200-187823400	Enhancers	HUVEC	blood vessel
8	chr4:187821200-187825200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr4:187821400-187821800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr4:187821400-187822000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr4:187821400-187822400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr4:187821400-187822600	Enhancers	K562	blood
13	chr4:187821400-187822600	Enhancers	Osteobl	bone
14	chr4:187821400-187823600	Enhancers	NH-A	brain
15	chr4:187821400-187826400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
16	chr4:187821600-187821800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
17	chr4:187821600-187821800	Enhancers	Lung	lung
18	chr4:187821600-187821800	Enhancers	Skeletal Muscle Male	skeletal muscle
19	chr4:187821600-187822000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr4:187821600-187822400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
21	chr4:187821600-187822400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
22	chr4:187821600-187822400	Enhancers	Hela-S3	cervix
23	chr4:187821600-187822400	Enhancers	NHEK	skin
24	chr4:187821600-187825400	Enhancers	Rectal Mucosa Donor 31	rectum
25	chr4:187821600-187826000	Enhancers	HepG2	liver
26	chr4:187821600-187826200	Enhancers	Adipose Nuclei	Adipose
27	chr4:187821600-187826200	Enhancers	HSMM	muscle
28	chr4:187821600-187826200	Enhancers	HSMMtube	muscle
29	chr4:187821600-187826400	Enhancers	Muscle Satellite Cultured Cells	--
30	chr4:187821600-187826400	Enhancers	NHDF-Ad	bronchial
31	chr4:187821800-187822000	Enhancers	Fetal Intestine Large	intestine
32	chr4:187821800-187822200	Enhancers	Rectal Smooth Muscle	rectum
33	chr4:187821800-187823000	Weak transcription	Lung	lung
34	chr4:187821800-187823000	Weak transcription	Skeletal Muscle Male	skeletal muscle
35	chr4:187821800-187823200	Enhancers	A549	lung
36	chr4:187821800-187824200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
37	chr4:187821800-187824800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
38	chr4:187821800-187826200	Enhancers	Liver	Liver
39	chr4:187822000-187822200	Enhancers	Duodenum Smooth Muscle	Duodenum
40	chr4:187822000-187822400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
41	chr4:187822000-187822400	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr4:187822000-187822600	Enhancers	Fetal Lung	lung
43	chr4:187822000-187822600	Enhancers	NHLF	lung
44	chr4:187822000-187823000	Weak transcription	Fetal Intestine Large	intestine
45	chr4:187822000-187823600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr4:187822000-187826200	Enhancers	Stomach Mucosa	stomach
47	chr4:187822200-187822600	Enhancers	Duodenum Mucosa	Duodenum
48	chr4:187822200-187822600	Weak transcription	Rectal Smooth Muscle	rectum
49	chr4:187822200-187824200	Enhancers	Fetal Intestine Small	intestine
50	chr4:187822400-187823400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

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