Variant report

Variant	nsv1005268
Chromosome Location	chr4:48444307-48484389
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	chr4:48483723-48484037	K562	blood:	n/a	n/a
2	ARID3A	chr4:48447770-48448033	K562	blood:	n/a	n/a
3	ARID3A	chr4:48447705-48448039	HepG2	liver:	n/a	n/a
4	ARID3A	chr4:48477763-48478047	K562	blood:	n/a	n/a
5	ATF1	chr4:48483638-48483988	K562	blood:	n/a	n/a
6	BHLHE40	chr4:48477903-48478176	K562	blood:	n/a	n/a
7	BHLHE40	chr4:48451314-48451472	K562	blood:	n/a	n/a
8	BHLHE40	chr4:48483691-48483965	K562	blood:	n/a	n/a
9	BHLHE40	chr4:48451181-48451478	HepG2	liver:	n/a	n/a
10	CBX3	chr4:48483613-48484010	K562	blood:	n/a	n/a
11	CCNT2	chr4:48483694-48483987	K562	blood:	n/a	n/a
12	CCNT2	chr4:48477848-48478194	K562	blood:	n/a	n/a
13	CEBPB	chr4:48449081-48449271	K562	blood:	n/a	chr4:48449123-48449134
14	CEBPB	chr4:48449081-48449253	HepG2	liver:	n/a	chr4:48449123-48449134
15	CEBPB	chr4:48455218-48455523	HepG2	liver:	n/a	chr4:48455395-48455406
16	CEBPB	chr4:48483480-48483916	K562	blood:	n/a	chr4:48483581-48483594 chr4:48483583-48483594
17	CEBPB	chr4:48453348-48453402	A549	lung:	n/a	n/a
18	CEBPB	chr4:48455275-48455473	K562	blood:	n/a	chr4:48455395-48455406
19	CEBPB	chr4:48449009-48449284	IMR90	lung:	n/a	chr4:48449123-48449134
20	CEBPD	chr4:48483548-48484092	K562	blood:	n/a	n/a
21	CEBPD	chr4:48483530-48484088	K562	blood:	n/a	n/a
22	CHD2	chr4:48483568-48483726	K562	blood:	n/a	n/a
23	CHD2	chr4:48478980-48479020	K562	blood:	n/a	n/a
24	CTCF	chr4:48447760-48447910	GM12872	blood:	n/a	chr4:48447831-48447847 chr4:48447832-48447853 chr4:48447830-48447848
25	CTCF	chr4:48447800-48447950	HCM	heart:	n/a	chr4:48447831-48447847 chr4:48447832-48447853 chr4:48447830-48447848
26	CTCF	chr4:48447662-48448082	SK-N-SH	brain:	n/a	chr4:48447831-48447847 chr4:48447832-48447853 chr4:48447830-48447848
27	CTCF	chr4:48447760-48447910	HMF	breast:	n/a	chr4:48447831-48447847 chr4:48447832-48447853 chr4:48447830-48447848
28	CTCF	chr4:48447780-48447930	Caco-2	colon:	n/a	chr4:48447831-48447847 chr4:48447832-48447853 chr4:48447830-48447848
29	CTCF	chr4:48448184-48448248	Gliobla	brain:	n/a	n/a
30	CTCF	chr4:48448120-48448270	GM12873	blood:	n/a	n/a
31	CTCF	chr4:48447763-48447870	GM20000	blood:	n/a	chr4:48447831-48447847 chr4:48447832-48447853 chr4:48447830-48447848
32	CTCF	chr4:48447780-48447930	HPAF	blood vessel:	n/a	chr4:48447831-48447847 chr4:48447832-48447853 chr4:48447830-48447848
33	CTCF	chr4:48447736-48447914	LNCaP	prostate:	n/a	chr4:48447831-48447847 chr4:48447832-48447853 chr4:48447830-48447848
34	CTCF	chr4:48447735-48447905	HepG2	liver:	n/a	chr4:48447831-48447847 chr4:48447832-48447853 chr4:48447830-48447848
35	CTCF	chr4:48478940-48479090	BE2_C	brain:	n/a	n/a
36	CTCF	chr4:48447740-48447890	NB4	blood:	n/a	chr4:48447831-48447847 chr4:48447832-48447853 chr4:48447830-48447848
37	CTCF	chr4:48447743-48447900	GM12878	blood:	n/a	chr4:48447831-48447847 chr4:48447832-48447853 chr4:48447830-48447848
38	CTCF	chr4:48447740-48447911	GM10248	blood:	n/a	chr4:48447831-48447847 chr4:48447832-48447853 chr4:48447830-48447848
39	CTCF	chr4:48448120-48448270	GM12867	blood:	n/a	n/a
40	CTCF	chr4:48447780-48447930	GM12864	blood:	n/a	chr4:48447831-48447847 chr4:48447832-48447853 chr4:48447830-48447848
41	CTCF	chr4:48447780-48447930	GM12874	blood:	n/a	chr4:48447831-48447847 chr4:48447832-48447853 chr4:48447830-48447848
42	CTCF	chr4:48447700-48447941	HUVEC	blood vessel:	n/a	chr4:48447831-48447847 chr4:48447832-48447853 chr4:48447830-48447848
43	CTCF	chr4:48447720-48447870	HVMF	connective:	n/a	chr4:48447831-48447847 chr4:48447832-48447853 chr4:48447830-48447848
44	CTCF	chr4:48447920-48448070	GM12864	blood:	n/a	n/a
45	CTCF	chr4:48447740-48447890	AG04450	lung:	n/a	chr4:48447831-48447847 chr4:48447832-48447853 chr4:48447830-48447848
46	CTCF	chr4:48447647-48447955	HepG2	liver:	n/a	chr4:48447831-48447847 chr4:48447832-48447853 chr4:48447830-48447848
47	CTCF	chr4:48447740-48447890	GM12865	blood:	n/a	chr4:48447831-48447847 chr4:48447832-48447853 chr4:48447830-48447848
48	CTCF	chr4:48477520-48477670	HFF	foreskin:	n/a	n/a
49	CTCF	chr4:48448160-48448310	GM12871	blood:	n/a	n/a
50	CTCF	chr4:48447740-48447890	HCPEpiC	choroid plexus:	n/a	chr4:48447831-48447847 chr4:48447832-48447853 chr4:48447830-48447848

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:48483244-48483294	CMK	blood:	n/a
2	chr4:48483244-48483294	PrEC	prostate:	n/a
3	chr4:48483244-48483294	ProgFib	skin:	n/a
4	chr4:48483244-48483294	T-47D	breast:	n/a
5	chr4:48483244-48483294	GM12892	blood:	n/a
6	chr4:48483244-48483294	HCT-116	colon:	n/a
7	chr4:48483244-48483294	GM06990	blood:	n/a
8	chr4:48483244-48483294	Hela-S3	cervix:	n/a
9	chr4:48483244-48483294	SAEC	small airway:	n/a
10	chr4:48483244-48483294	IMR90	lung:	fetal
11	chr4:48483244-48483294	HPAEpiC	pulmonary alveolar:	n/a
12	chr4:48483244-48483294	HIPEpiC	eye:	n/a
13	chr4:48483244-48483294	HL-60	blood:	n/a
14	chr4:48483244-48483294	HCM	heart:	n/a
15	chr4:48483244-48483294	MCF10A-Er-Src	breast:	n/a
16	chr4:48483244-48483294	HRCEpiC	kidney:	n/a
17	chr4:48483244-48483294	AG09309	skin:	n/a
18	chr4:48483244-48483294	SK-N-MC	brain:	n/a
19	chr4:48483244-48483294	HEEpiC	esophagus:	n/a
20	chr4:48483244-48483294	AG04449	skin:	fetal
21	chr4:48483244-48483294	U87	brain:	n/a
22	chr4:48483244-48483294	HRPEpiC	eye:	n/a
23	chr4:48483244-48483294	GM19239	blood:	n/a
24	chr4:48483244-48483294	GM12878	blood:	n/a
25	chr4:48483244-48483294	HMEC	breast:	n/a
26	chr4:48483244-48483294	RPTEC	kidney:	n/a
27	chr4:48483244-48483294	HEK293	kidney:	embryo
28	chr4:48483244-48483294	SKMC	muscle:	n/a
29	chr4:48483244-48483294	SK-N-SH	brain:	n/a
30	chr4:48483244-48483294	AG10803	skin:	n/a
31	chr4:48483244-48483294	LNCaP	prostate:	n/a
32	chr4:48483244-48483294	NH-A	brain:	n/a
33	chr4:48483244-48483294	HepG2	liver:	n/a
34	chr4:48483244-48483294	AoSMC	blood vessel:	n/a
35	chr4:48483244-48483294	PFSK-1	brain:	n/a
36	chr4:48483244-48483294	Hepatocyte	liver:	n/a
37	chr4:48483244-48483294	NB4	blood:	n/a
38	chr4:48483244-48483294	GM12891	blood:	n/a
39	chr4:48483244-48483294	AG09319	gingival:	n/a
40	chr4:48483244-48483294	NHBE	bronchial:	n/a
41	chr4:48483244-48483294	K562	blood:	n/a
42	chr4:48483244-48483294	Jurkat	blood:	n/a
43	chr4:48483244-48483294	ovcar-3	ovarian:	n/a
44	chr4:48483244-48483294	H1-hESC	embryonic stem cell:	embryo
45	chr4:48483244-48483294	SK-N-SH_RA	brain:	n/a
46	chr4:48483244-48483294	PANC-1	pancreas:	n/a
47	chr4:48483244-48483294	HNPCEpiC	eye:	n/a
48	chr4:48483244-48483294	A549	lung:	n/a
49	chr4:48483244-48483294	BJ	skin:	n/a
50	chr4:48483244-48483294	NT2-D1	testis:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:48478979..48481680-chr4:48482843..48484535,2	K562	blood:
2	chr4:48462803..48464644-chr4:48465855..48467881,2	K562	blood:
3	chr4:48447376..48448138-chr4:48683597..48684250,2	K562	blood:
4	chr4:48456400..48458148-chr4:48459836..48461685,2	K562	blood:
5	chr4:48341467..48343836-chr4:48476769..48479508,2	K562	blood:
6	chr4:48465348..48467706-chr4:48469916..48472913,2	K562	blood:
7	chr4:48461047..48463475-chr4:48463503..48465946,2	MCF-7	breast:
8	chr4:48461047..48463475-chr4:48463503..48465946,2	MCF-7	breast:
9	chr4:48443452..48446386-chr4:48450705..48452987,2	K562	blood:
10	chr4:48474711..48478093-chr4:48481760..48484353,3	K562	blood:
11	chr4:48447877..48448560-chr4:48548331..48548864,2	MCF-7	breast:
12	chr4:48443452..48446386-chr4:48450705..48452987,2	K562	blood:
13	chr4:48473818..48475564-chr4:48478853..48480558,2	K562	blood:
14	chr4:48477174..48479386-chr4:48484669..48486658,3	K562	blood:
15	chr4:48473818..48475564-chr4:48478853..48480558,2	K562	blood:
16	chr4:48470613..48473605-chr4:48483199..48486711,3	K562	blood:
17	chr4:48454110..48457080-chr4:48459729..48462121,2	K562	blood:
18	chr4:48456400..48458148-chr4:48459836..48461685,2	K562	blood:
19	chr4:48478979..48481680-chr4:48482843..48484535,2	K562	blood:
20	chr4:48465348..48467706-chr4:48469916..48472913,2	K562	blood:
21	chr4:48484114..48487251-chr4:48504187..48509460,5	K562	blood:
22	chr4:48454110..48457080-chr4:48459729..48462121,2	K562	blood:
23	chr4:48341909..48343469-chr4:48483589..48486077,2	K562	blood:
24	chr4:48474711..48478093-chr4:48481760..48484353,3	K562	blood:
25	chr4:48462803..48464644-chr4:48465855..48467881,2	K562	blood:
26	chr4:48478067..48481410-chr4:48493413..48496125,3	K562	blood:

Variant related genes	Relation type
SLC10A4	TF binding region
SLC10A4	CpG island
ENSG00000145248	chromatin interactions
ENSG00000075539	chromatin interactions
ENSG00000109171	chromatin interactions

Extended variants
information (count: 1025 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:1025 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs140768477	chr4:48447898-48447899	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs548316056	chr4:48447920-48447921	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs531262419	chr4:48447964-48447965	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs114581763	chr4:48447983-48447984	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs534927161	chr4:48447986-48447987	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs191433261	chr4:48448011-48448012	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs149494493	chr4:48448012-48448013	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs182058784	chr4:48448036-48448037	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs557230002	chr4:48448045-48448046	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs186983005	chr4:48448049-48448050	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs372946171	chr4:48448051-48448052	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs115000421	chr4:48448057-48448058	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs567887643	chr4:48448096-48448097	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs199531953	chr4:48448152-48448153	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs554662227	chr4:48448170-48448171	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs573262625	chr4:48448178-48448179	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs528573017	chr4:48448188-48448189	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs372742972	chr4:48448196-48448197	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs377205008	chr4:48448221-48448222	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs540354197	chr4:48448249-48448250	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs192319298	chr4:48448278-48448279	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs183424415	chr4:48448326-48448327	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs546645538	chr4:48448366-48448367	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs571418667	chr4:48448370-48448371	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs538617732	chr4:48448371-48448372	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs186640007	chr4:48448378-48448379	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs550585695	chr4:48448382-48448383	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs529729898	chr4:48448383-48448384	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs548179301	chr4:48448456-48448457	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs566320886	chr4:48448458-48448459	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs527284044	chr4:48448477-48448478	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs182473418	chr4:48448613-48448614	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs7659631	chr4:48448614-48448615	Enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
34	rs148487966	chr4:48448635-48448636	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs569175931	chr4:48448649-48448650	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs536270974	chr4:48448698-48448699	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs371408318	chr4:48448786-48448787	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs113025148	chr4:48448825-48448826	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs540765889	chr4:48448853-48448854	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs558731627	chr4:48448857-48448858	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs188328501	chr4:48448901-48448902	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs544387027	chr4:48448946-48448947	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs537386091	chr4:48448986-48448987	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs562792840	chr4:48449004-48449005	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs574812157	chr4:48449144-48449145	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs77389305	chr4:48449213-48449214	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs573827482	chr4:48449217-48449218	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs534820507	chr4:48449267-48449268	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs192850200	chr4:48449270-48449271	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs143149209	chr4:48449292-48449293	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:62)

Disease	PMID	Source
Colorectal cancer	19359472	CNVD
Neuroblastoma	17533364	CNVD
Oral squamous cell carcinoma	17134496	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Cancer	21637783	CNVD
Melanoma	21693616	CNVD
Squamous cell cancer	21044232	CNVD
Colorectal cancer	20709793	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Non-small cell lung cancer	21044232	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Cervical cancer	21062161	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	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
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	22183965	CNVD
Cancer	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
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Basal cell lymphoma	21115979	CNVD
Breast cancer	22522925	CNVD
Parkinson disease	18923514	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
small cell lung cancer	20016488	CNVD

Chromatin state (count:95 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:48448600-48449000	Enhancers	Osteobl	bone
2	chr4:48449000-48452800	Weak transcription	Osteobl	bone
3	chr4:48451000-48451800	Enhancers	HepG2	liver
4	chr4:48451200-48451400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr4:48451200-48451800	Enhancers	K562	blood
6	chr4:48452200-48457600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
7	chr4:48452800-48453200	Enhancers	Cortex derived primary cultured neurospheres	brain
8	chr4:48452800-48453200	Flanking Active TSS	Osteobl	bone
9	chr4:48452800-48453400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
10	chr4:48452800-48453600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
11	chr4:48452800-48453600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr4:48453000-48453600	Enhancers	Fetal Brain Male	brain
13	chr4:48453200-48453600	Enhancers	Osteobl	bone
14	chr4:48462600-48463400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr4:48463400-48463800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr4:48463400-48464000	Enhancers	Duodenum Mucosa	Duodenum
17	chr4:48464000-48464400	Weak transcription	Duodenum Mucosa	Duodenum
18	chr4:48464400-48465000	Enhancers	Duodenum Mucosa	Duodenum
19	chr4:48464400-48465400	Enhancers	Brain Germinal Matrix	brain
20	chr4:48464400-48471600	Weak transcription	Cortex derived primary cultured neurospheres	brain
21	chr4:48467600-48467800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr4:48467800-48468600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr4:48468600-48469800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr4:48469400-48469800	Enhancers	Brain Hippocampus Middle	brain
25	chr4:48469600-48470000	Active TSS	NHDF-Ad	bronchial
26	chr4:48469600-48470000	Enhancers	Osteobl	bone
27	chr4:48469800-48470000	Enhancers	Brain Germinal Matrix	brain
28	chr4:48469800-48471600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr4:48469800-48471600	Weak transcription	Brain Hippocampus Middle	brain
30	chr4:48470000-48470200	Enhancers	NHDF-Ad	bronchial
31	chr4:48470000-48471600	Weak transcription	Brain Germinal Matrix	brain
32	chr4:48470000-48474400	Weak transcription	Osteobl	bone
33	chr4:48471600-48472400	Enhancers	Brain Substantia Nigra	brain
34	chr4:48471600-48472600	Enhancers	Brain Hippocampus Middle	brain
35	chr4:48471600-48473000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr4:48471600-48473200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr4:48471600-48473400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr4:48471600-48473400	Enhancers	Brain Cingulate Gyrus	brain
39	chr4:48471600-48473600	Enhancers	Cortex derived primary cultured neurospheres	brain
40	chr4:48471600-48473600	Enhancers	Brain Germinal Matrix	brain
41	chr4:48471800-48472600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
42	chr4:48472200-48473000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
43	chr4:48472200-48473000	Enhancers	HSMMtube	muscle
44	chr4:48472400-48472600	Enhancers	Brain Anterior Caudate	brain
45	chr4:48472400-48473000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
46	chr4:48472400-48473000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
47	chr4:48472400-48473000	Enhancers	Muscle Satellite Cultured Cells	--
48	chr4:48472400-48473000	Flanking Active TSS	Brain Substantia Nigra	brain
49	chr4:48472400-48473200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
50	chr4:48472400-48473200	Enhancers	HSMM	muscle

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