Variant report

Variant	nsv879022
Chromosome Location	chr4:56617884-56668431
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	ATF3	chr4:56634460-56634806	K562	blood:	n/a	n/a
2	BRCA1	chr4:56620954-56621308	Hela-S3	cervix:	n/a	n/a
3	CEBPB	chr4:56641163-56641332	H1-hESC	embryonic stem cell:	n/a	n/a
4	CEBPB	chr4:56634497-56634766	IMR90	lung:	n/a	n/a
5	CEBPB	chr4:56634464-56634798	H1-hESC	embryonic stem cell:	n/a	n/a
6	CEBPB	chr4:56636914-56637145	MCF-7	breast:	n/a	n/a
7	CEBPB	chr4:56625672-56625694	K562	blood:	n/a	n/a
8	CEBPB	chr4:56634462-56634808	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr4:56661828-56662109	HepG2	liver:	n/a	chr4:56661947-56661958
10	CEBPB	chr4:56657330-56657634	HepG2	liver:	n/a	chr4:56657474-56657485
11	CEBPB	chr4:56634474-56634722	HepG2	liver:	n/a	n/a
12	CEBPB	chr4:56620956-56621356	IMR90	lung:	n/a	chr4:56621186-56621197 chr4:56621186-56621199
13	CEBPB	chr4:56620886-56621412	Hela-S3	cervix:	n/a	chr4:56621186-56621197 chr4:56621186-56621199
14	CEBPB	chr4:56634514-56634767	K562	blood:	n/a	n/a
15	CEBPB	chr4:56639917-56640085	K562	blood:	n/a	n/a
16	CHD2	chr4:56650923-56651165	H1-hESC	embryonic stem cell:	n/a	n/a
17	CHD2	chr4:56650906-56651262	K562	blood:	n/a	n/a
18	CHD2	chr4:56640637-56640667	K562	blood:	n/a	n/a
19	CTCF	chr4:56659400-56659550	HCM	heart:	n/a	n/a
20	CTCF	chr4:56633141-56633181	K562	blood:	n/a	n/a
21	CTCF	chr4:56633065-56633224	K562	blood:	n/a	n/a
22	CTCF	chr4:56659400-56659550	HAc	cerebellar:	n/a	n/a
23	CTCF	chr4:56659440-56659590	AG09319	gingival:	n/a	n/a
24	CTCF	chr4:56659440-56659590	HPF	lung:	n/a	n/a
25	CTCF	chr4:56659420-56659570	HPAF	blood vessel:	n/a	n/a
26	CTCF	chr4:56659560-56659710	HCPEpiC	choroid plexus:	n/a	n/a
27	CUX1	chr4:56623771-56623777	K562	blood:	n/a	n/a
28	E2F4	chr4:56621149-56621208	MCF10A-Er-Src	breast:	n/a	n/a
29	E2F4	chr4:56626861-56626865	MCF10A-Er-Src	breast:	n/a	n/a
30	E2F4	chr4:56634505-56634776	MCF10A-Er-Src	breast:	n/a	n/a
31	EBF1	chr4:56618794-56619032	GM12878	blood:	n/a	n/a
32	EP300	chr4:56620984-56621503	Hela-S3	cervix:	n/a	n/a
33	EP300	chr4:56619067-56619267	GM12878	blood:	n/a	chr4:56619164-56619178
34	EP300	chr4:56647689-56647692	K562	blood:	n/a	n/a
35	ETS1	chr4:56650902-56651188	GM12878	blood:	n/a	n/a
36	FOS	chr4:56636976-56637153	MCF10A-Er-Src	breast:	n/a	n/a
37	FOS	chr4:56634480-56634869	MCF10A-Er-Src	breast:	n/a	chr4:56634676-56634687
38	FOS	chr4:56620527-56621577	MCF10A-Er-Src	breast:	n/a	chr4:56620693-56620701 chr4:56621135-56621147 chr4:56621137-56621145 chr4:56620689-56620700 chr4:56621092-56621103 chr4:56620691-56620703 chr4:56621135-56621146
39	FOS	chr4:56634442-56634871	MCF10A-Er-Src	breast:	n/a	chr4:56634676-56634687
40	FOS	chr4:56620566-56621768	HUVEC	blood vessel:	n/a	chr4:56620693-56620701 chr4:56621135-56621147 chr4:56621137-56621145 chr4:56620689-56620700 chr4:56621624-56621631 chr4:56621092-56621103 chr4:56621624-56621632 chr4:56620691-56620703 chr4:56621624-56621632 chr4:56621135-56621146
41	FOS	chr4:56620159-56621462	MCF10A-Er-Src	breast:	n/a	chr4:56620447-56620457 chr4:56620693-56620701 chr4:56621135-56621147 chr4:56621137-56621145 chr4:56620689-56620700 chr4:56621092-56621103 chr4:56620691-56620703 chr4:56621135-56621146
42	FOS	chr4:56624307-56624493	MCF10A-Er-Src	breast:	n/a	n/a
43	FOS	chr4:56657793-56658099	MCF10A-Er-Src	breast:	n/a	n/a
44	FOS	chr4:56634472-56634858	MCF10A-Er-Src	breast:	n/a	chr4:56634676-56634687
45	FOS	chr4:56636997-56637159	MCF10A-Er-Src	breast:	n/a	n/a
46	FOS	chr4:56620172-56620294	MCF10A-Er-Src	breast:	n/a	n/a
47	FOS	chr4:56657790-56658106	MCF10A-Er-Src	breast:	n/a	n/a
48	FOS	chr4:56636945-56637099	MCF10A-Er-Src	breast:	n/a	n/a
49	FOS	chr4:56634434-56635078	HUVEC	blood vessel:	n/a	chr4:56634676-56634687
50	FOS	chr4:56620932-56621329	MCF10A-Er-Src	breast:	n/a	chr4:56621135-56621147 chr4:56621137-56621145 chr4:56621092-56621103 chr4:56621135-56621146

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:56660460-56660510	BE2_C	brain:	n/a
2	chr4:56659922-56659972	SAEC	small airway:	n/a
3	chr4:56660460-56660510	BE2_C	brain:	n/a
4	chr4:56659922-56659972	SAEC	small airway:	n/a
5	chr4:56663994-56664044	SK-N-SH	brain:	n/a
6	chr4:56659922-56659972	ovcar-3	ovarian:	n/a
7	chr4:56660143-56660193	GM12892	blood:	n/a
8	chr4:56659985-56660035	HIPEpiC	eye:	n/a
9	chr4:56659985-56660035	PANC-1	pancreas:	n/a
10	chr4:56659770-56659820	U87	brain:	n/a
11	chr4:56658357-56658407	T-47D	breast:	n/a
12	chr4:56659922-56659972	HAEpiC	amniotic membrane:	n/a
13	chr4:56659985-56660035	U87	brain:	n/a
14	chr4:56659922-56659972	GM12891	blood:	n/a
15	chr4:56663994-56664044	T-47D	breast:	n/a
16	chr4:56658357-56658407	LNCaP	prostate:	n/a
17	chr4:56660328-56660378	HUVEC	blood vessel:	n/a
18	chr4:56659922-56659972	NT2-D1	testis:	n/a
19	chr4:56659985-56660035	ProgFib	skin:	n/a
20	chr4:56660398-56660448	HMEC	breast:	n/a
21	chr4:56659985-56660035	AG09309	skin:	n/a
22	chr4:56659922-56659972	HRE	kidney:	n/a
23	chr4:56659985-56660035	BE2_C	brain:	n/a
24	chr4:56659985-56660035	NH-A	brain:	n/a
25	chr4:56659922-56659972	GM12892	blood:	n/a
26	chr4:56660398-56660448	HEK293	kidney:	embryo
27	chr4:56658357-56658407	HAEpiC	amniotic membrane:	n/a
28	chr4:56660143-56660193	BJ	skin:	n/a
29	chr4:56659770-56659820	HRPEpiC	eye:	n/a
30	chr4:56660460-56660510	GM12878	blood:	n/a
31	chr4:56659922-56659972	NHDF-neo	bronchial:	n/a
32	chr4:56660143-56660193	AoSMC	blood vessel:	n/a
33	chr4:56660143-56660193	HCF	heart:	n/a
34	chr4:56660143-56660193	AG09319	gingival:	n/a
35	chr4:56659922-56659972	A549	lung:	n/a
36	chr4:56660143-56660193	T-47D	breast:	n/a
37	chr4:56660328-56660378	HNPCEpiC	eye:	n/a
38	chr4:56663994-56664044	HRCEpiC	kidney:	n/a
39	chr4:56660328-56660378	LNCaP	prostate:	n/a
40	chr4:56659985-56660035	SK-N-SH	brain:	n/a
41	chr4:56659770-56659820	Hepatocyte	liver:	n/a
42	chr4:56659770-56659820	A549	lung:	n/a
43	chr4:56658357-56658407	ovcar-3	ovarian:	n/a
44	chr4:56656788-56656838	HEEpiC	esophagus:	n/a
45	chr4:56659770-56659820	HAEpiC	amniotic membrane:	n/a
46	chr4:56659770-56659820	NT2-D1	testis:	n/a
47	chr4:56658357-56658407	GM12878	blood:	n/a
48	chr4:56656788-56656838	H1-hESC	embryonic stem cell:	embryo
49	chr4:56660143-56660193	ECC-1	luminal epithelium:	n/a
50	chr4:56660398-56660448	HCM	heart:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:56632143..56634833-chr4:56645255..56648181,2	K562	blood:
2	chr4:56649556..56651202-chr4:56652557..56654365,2	K562	blood:
3	chr4:56632143..56634650-chr4:56645244..56648181,2	K562	blood:
4	chr4:56631564..56634040-chr4:56635751..56638538,2	K562	blood:
5	chr4:56631566..56634040-chr4:56636504..56638538,3	K562	blood:
6	chr4:56632143..56634650-chr4:56645244..56648181,2	K562	blood:
7	chr4:56637542..56640482-chr4:56658130..56659977,2	K562	blood:
8	chr4:56637542..56640482-chr4:56658130..56659977,2	K562	blood:
9	chr4:56631564..56634040-chr4:56635751..56638538,2	K562	blood:
10	chr4:56637771..56639865-chr4:56697633..56699417,2	MCF-7	breast:
11	chr4:56632143..56634833-chr4:56645255..56648181,2	K562	blood:
12	chr4:56613502..56615482-chr4:56616796..56619425,2	K562	blood:
13	chr4:56649556..56651202-chr4:56652557..56654365,2	K562	blood:
14	chr4:56631566..56634040-chr4:56636504..56638538,3	K562	blood:

Variant related genes	Relation type
RNU6-276P	TF binding region
RNU6-276P	CpG island

Extended variants
information (count: 1243 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:1243 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4519853	chr4:56617884-56617885	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs554911121	chr4:56617893-56617894	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs530667354	chr4:56617928-56617929	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs550858632	chr4:56617974-56617975	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs539065763	chr4:56617991-56617992	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs184525621	chr4:56617993-56617994	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs73817250	chr4:56618006-56618007	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs35460247	chr4:56618018-56618019	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs565821818	chr4:56618022-56618023	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs76271148	chr4:56618042-56618043	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs28477533	chr4:56618095-56618096	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs71599701	chr4:56618146-56618147	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs189233239	chr4:56618220-56618221	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs200882745	chr4:56618281-56618282	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs541275194	chr4:56618289-56618290	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs552991032	chr4:56618312-56618313	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs577909942	chr4:56618317-56618318	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs537306389	chr4:56618323-56618324	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs115084157	chr4:56618342-56618343	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs73149888	chr4:56618344-56618345	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs543226782	chr4:56618394-56618395	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs113938702	chr4:56618397-56618398	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs116685495	chr4:56618402-56618403	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs113184603	chr4:56618483-56618484	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs531812501	chr4:56618515-56618516	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs77698481	chr4:56618561-56618562	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs543961476	chr4:56618585-56618586	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs530514677	chr4:56618602-56618603	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs375272258	chr4:56618605-56618606	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs147604032	chr4:56618606-56618607	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs540278694	chr4:56618686-56618687	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs73238322	chr4:56618718-56618719	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs529973381	chr4:56618719-56618720	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs546357661	chr4:56618722-56618723	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs181130537	chr4:56618770-56618771	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs528530025	chr4:56618829-56618830	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs33937025	chr4:56618849-56618850	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs398083087	chr4:56618854-56618855	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs397993450	chr4:56618855-56618856	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs199787115	chr4:56618856-56618857	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs11936045	chr4:56618864-56618865	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs547815616	chr4:56618900-56618901	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs559784240	chr4:56618948-56618949	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs142290486	chr4:56618950-56618951	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs552296122	chr4:56619014-56619015	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs537430763	chr4:56619071-56619072	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs146110987	chr4:56619107-56619108	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs75751869	chr4:56619126-56619127	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs536964858	chr4:56619128-56619129	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs186364905	chr4:56619167-56619168	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:90)

Disease	PMID	Source
Gastrointestinal stromal cancer	16982739	CNVD
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
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	22183965	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Lung cancer	18438408	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	21922591	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Parkinson disease	21956041	CNVD
Mental retardation	20522426	CNVD
delayed speech	20522426	CNVD
growth disorder	20522426	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Parkinson disease	18923514	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Breast cancer	16272173	CNVD
Glioblastoma multiforme	19435819	CNVD
Multiple myeloma	16616336	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
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
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Ovarian neoplasms	16753589	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Glioblastoma	17504929	CNVD
Glioblastoma	16823502	CNVD
Melanoma	16908931	CNVD
Glioblastoma	20031968	CNVD
Medulloblastoma	19270706	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Olfactory neuroblastoma	18408657	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Rhabdomyosarcoma	16790082	CNVD
Gastrointestinal stromal cancer	17438095	CNVD
Colorectal cancer	16272173	CNVD
Lung cancer	19208797	CNVD
small cell lung cancer	20016488	CNVD
Glioblastoma multiforme	19115005	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	21138945	CNVD
Cancer	22183965	CNVD
Autism	22543975	CNVD
Breast cancer	21785460	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:237 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:56615600-56622800	Weak transcription	K562	blood
2	chr4:56620000-56625000	Enhancers	Hela-S3	cervix
3	chr4:56620200-56624800	Enhancers	HUVEC	blood vessel
4	chr4:56620400-56622000	Enhancers	NHEK	skin
5	chr4:56620400-56622200	Enhancers	HMEC	breast
6	chr4:56620600-56621800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr4:56620600-56621800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr4:56620600-56622000	Enhancers	Muscle Satellite Cultured Cells	--
9	chr4:56620600-56622200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr4:56620600-56622200	Enhancers	NHDF-Ad	bronchial
11	chr4:56620800-56621800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr4:56621000-56621200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr4:56621200-56621400	Enhancers	Osteobl	bone
14	chr4:56621800-56623800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr4:56621800-56624600	Weak transcription	Osteobl	bone
16	chr4:56622000-56624000	Weak transcription	Muscle Satellite Cultured Cells	--
17	chr4:56622200-56622600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr4:56622200-56622600	Weak transcription	HMEC	breast
19	chr4:56622200-56623800	Weak transcription	NHDF-Ad	bronchial
20	chr4:56622600-56624000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr4:56622600-56624000	Enhancers	HMEC	breast
22	chr4:56622800-56623000	Enhancers	H9 Cell Line	embryonic stem cell
23	chr4:56622800-56625000	Enhancers	ES-I3 Cell Line	embryonic stem cell
24	chr4:56622800-56625000	Enhancers	K562	blood
25	chr4:56623000-56623200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr4:56623000-56623200	Enhancers	Colonic Mucosa	Colon
27	chr4:56623200-56623400	Enhancers	Right Atrium	heart
28	chr4:56623200-56623800	Enhancers	Sigmoid Colon	Sigmoid Colon
29	chr4:56623200-56624000	Enhancers	HepG2	liver
30	chr4:56623200-56625000	Enhancers	Stomach Mucosa	stomach
31	chr4:56623400-56624400	Enhancers	iPS-15b Cell Line	embryonic stem cell
32	chr4:56623400-56624400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr4:56623400-56624600	Weak transcription	Colonic Mucosa	Colon
34	chr4:56623400-56624600	Weak transcription	Right Atrium	heart
35	chr4:56623600-56623800	Enhancers	H9 Cell Line	embryonic stem cell
36	chr4:56623600-56624000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
37	chr4:56623600-56624200	Enhancers	iPS-18 Cell Line	embryonic stem cell
38	chr4:56623600-56625800	Enhancers	Rectal Mucosa Donor 31	rectum
39	chr4:56623800-56625200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr4:56623800-56625200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr4:56623800-56625200	Enhancers	NHDF-Ad	bronchial
42	chr4:56624000-56624400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
43	chr4:56624000-56624400	Enhancers	Duodenum Mucosa	Duodenum
44	chr4:56624000-56624800	Enhancers	HUES64 Cell Line	embryonic stem cell
45	chr4:56624000-56625000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
46	chr4:56624000-56625000	Enhancers	Muscle Satellite Cultured Cells	--
47	chr4:56624200-56625200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr4:56624200-56625800	Enhancers	Rectal Mucosa Donor 29	rectum
49	chr4:56624400-56624600	Enhancers	Pancreatic Islets	Pancreatic Islet
50	chr4:56624400-56625000	Enhancers	Skeletal Muscle Female	skeletal muscle

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