Variant report

Variant	nsv829925
Chromosome Location	chr4:48467693-48639342
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1571)
CpG islands
(count:2204)
Chromatin interactive
region (count:115)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1571 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:48533201-48533219	K562	blood:	n/a	n/a
2	ARID3A	chr4:48580424-48580701	HepG2	liver:	n/a	n/a
3	ARID3A	chr4:48625256-48625761	K562	blood:	n/a	n/a
4	ARID3A	chr4:48484962-48485247	K562	blood:	n/a	n/a
5	ARID3A	chr4:48625367-48625761	HepG2	liver:	n/a	n/a
6	ARID3A	chr4:48477763-48478047	K562	blood:	n/a	n/a
7	ARID3A	chr4:48483723-48484037	K562	blood:	n/a	n/a
8	ARID3A	chr4:48593472-48593744	K562	blood:	n/a	n/a
9	ARID3A	chr4:48487020-48487153	K562	blood:	n/a	n/a
10	ARID3A	chr4:48506369-48506683	K562	blood:	n/a	n/a
11	ARID3A	chr4:48628294-48628494	K562	blood:	n/a	n/a
12	ARID3A	chr4:48605411-48605798	HepG2	liver:	n/a	n/a
13	ARID3A	chr4:48597297-48597435	K562	blood:	n/a	n/a
14	ATF1	chr4:48483638-48483988	K562	blood:	n/a	n/a
15	ATF1	chr4:48631400-48631866	K562	blood:	n/a	n/a
16	ATF1	chr4:48593488-48593917	K562	blood:	n/a	n/a
17	ATF1	chr4:48625474-48625805	K562	blood:	n/a	n/a
18	ATF2	chr4:48501607-48502148	GM12878	blood:	n/a	n/a
19	ATF2	chr4:48501459-48502226	GM12878	blood:	n/a	n/a
20	ATF3	chr4:48580349-48580732	K562	blood:	n/a	n/a
21	ATF3	chr4:48578069-48578255	K562	blood:	n/a	n/a
22	BACH1	chr4:48493250-48493536	H1-hESC	embryonic stem cell:	n/a	n/a
23	BACH1	chr4:48506422-48506590	K562	blood:	n/a	n/a
24	BACH1	chr4:48501052-48501115	H1-hESC	embryonic stem cell:	n/a	n/a
25	BACH1	chr4:48639268-48639335	H1-hESC	embryonic stem cell:	n/a	n/a
26	BACH1	chr4:48486855-48487010	H1-hESC	embryonic stem cell:	n/a	n/a
27	BACH1	chr4:48520028-48520120	K562	blood:	n/a	n/a
28	BACH1	chr4:48485777-48486288	H1-hESC	embryonic stem cell:	n/a	n/a
29	BACH1	chr4:48485381-48485382	H1-hESC	embryonic stem cell:	n/a	n/a
30	BATF	chr4:48501757-48502084	GM12878	blood:	n/a	n/a
31	BATF	chr4:48501720-48502070	GM12878	blood:	n/a	n/a
32	BHLHE40	chr4:48501765-48502234	GM12878	blood:	n/a	n/a
33	BHLHE40	chr4:48486934-48487121	K562	blood:	n/a	n/a
34	BHLHE40	chr4:48593502-48593748	K562	blood:	n/a	n/a
35	BHLHE40	chr4:48485470-48485714	K562	blood:	n/a	chr4:48485560-48485576
36	BHLHE40	chr4:48477903-48478176	K562	blood:	n/a	n/a
37	BHLHE40	chr4:48483691-48483965	K562	blood:	n/a	n/a
38	CBX3	chr4:48637224-48637834	HCT-116	colon:	n/a	n/a
39	CBX3	chr4:48485746-48486116	K562	blood:	n/a	n/a
40	CBX3	chr4:48625219-48625838	K562	blood:	n/a	chr4:48625531-48625542
41	CBX3	chr4:48483613-48484010	K562	blood:	n/a	n/a
42	CCNT2	chr4:48510600-48510755	K562	blood:	n/a	n/a
43	CCNT2	chr4:48486352-48486939	K562	blood:	n/a	n/a
44	CCNT2	chr4:48477848-48478194	K562	blood:	n/a	n/a
45	CCNT2	chr4:48485129-48486088	K562	blood:	n/a	n/a
46	CCNT2	chr4:48492468-48492539	K562	blood:	n/a	n/a
47	CCNT2	chr4:48499832-48499865	K562	blood:	n/a	n/a
48	CCNT2	chr4:48631618-48631818	K562	blood:	n/a	n/a
49	CCNT2	chr4:48625537-48625759	K562	blood:	n/a	n/a
50	CCNT2	chr4:48483694-48483987	K562	blood:	n/a	n/a

(count:2204 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:48485624-48485674	NH-A	brain:	n/a
2	chr4:48493420-48493470	HEK293	kidney:	embryo
3	chr4:48496404-48496454	ECC-1	luminal epithelium:	n/a
4	chr4:48485289-48485339	HRCEpiC	kidney:	n/a
5	chr4:48486087-48486137	BJ	skin:	n/a
6	chr4:48485293-48485343	K562	blood:	n/a
7	chr4:48483244-48483294	HEEpiC	esophagus:	n/a
8	chr4:48501509-48501559	HRPEpiC	eye:	n/a
9	chr4:48485624-48485674	NH-A	brain:	n/a
10	chr4:48493420-48493470	HEK293	kidney:	embryo
11	chr4:48496404-48496454	ECC-1	luminal epithelium:	n/a
12	chr4:48485289-48485339	HRCEpiC	kidney:	n/a
13	chr4:48486087-48486137	BJ	skin:	n/a
14	chr4:48485293-48485343	K562	blood:	n/a
15	chr4:48483244-48483294	HEEpiC	esophagus:	n/a
16	chr4:48501509-48501559	HRPEpiC	eye:	n/a
17	chr4:48485328-48485378	SK-N-SH_RA	brain:	n/a
18	chr4:48489221-48489271	NH-A	brain:	n/a
19	chr4:48485301-48485351	GM12878	blood:	n/a
20	chr4:48489221-48489271	RPTEC	kidney:	n/a
21	chr4:48485569-48485619	SK-N-MC	brain:	n/a
22	chr4:48485301-48485351	ECC-1	luminal epithelium:	n/a
23	chr4:48493846-48493896	AoSMC	blood vessel:	n/a
24	chr4:48485624-48485674	AoSMC	blood vessel:	n/a
25	chr4:48485289-48485339	ECC-1	luminal epithelium:	n/a
26	chr4:48496404-48496454	HRCEpiC	kidney:	n/a
27	chr4:48485289-48485339	LNCaP	prostate:	n/a
28	chr4:48492344-48492394	Hela-S3	cervix:	n/a
29	chr4:48491941-48491991	NB4	blood:	n/a
30	chr4:48489221-48489271	AG10803	skin:	n/a
31	chr4:48492304-48492354	GM12878	blood:	n/a
32	chr4:48493846-48493896	AG09309	skin:	n/a
33	chr4:48492304-48492354	MCF-7	breast:	n/a
34	chr4:48492225-48492275	HCT-116	colon:	n/a
35	chr4:48485293-48485343	HAEpiC	amniotic membrane:	n/a
36	chr4:48486785-48486835	Jurkat	blood:	n/a
37	chr4:48492845-48492895	AG04449	skin:	fetal
38	chr4:48489221-48489271	HPAEpiC	pulmonary alveolar:	n/a
39	chr4:48492848-48492898	A549	lung:	n/a
40	chr4:48492118-48492168	HPAEpiC	pulmonary alveolar:	n/a
41	chr4:48486785-48486835	HEEpiC	esophagus:	n/a
42	chr4:48485090-48485140	AG04450	lung:	fetal
43	chr4:48492344-48492394	BJ	skin:	n/a
44	chr4:48492304-48492354	Jurkat	blood:	n/a
45	chr4:48492196-48492246	NB4	blood:	n/a
46	chr4:48486154-48486204	BE2_C	brain:	n/a
47	chr4:48486316-48486366	HRCEpiC	kidney:	n/a
48	chr4:48492344-48492394	SAEC	small airway:	n/a
49	chr4:48485293-48485343	AG04450	lung:	fetal
50	chr4:48485233-48485283	GM12878	blood:	n/a

(count:115 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr4:48492886..48494734-chr4:48535449..48537970,2	K562	blood:
2	chr4:48518871..48522013-chr4:48524395..48528257,3	K562	blood:
3	chr4:48586327..48590238-chr4:48780231..48783624,4	MCF-7	breast:
4	chr4:48540734..48543756-chr4:48544156..48546827,3	K562	blood:
5	chr4:48435674..48437521-chr4:48577524..48579484,2	K562	blood:
6	chr4:48573447..48576202-chr4:48576256..48578868,3	K562	blood:
7	chr4:48477174..48479386-chr4:48484669..48486658,3	K562	blood:
8	chr4:48484114..48487251-chr4:48504187..48509460,5	K562	blood:
9	chr4:48462803..48464644-chr4:48465855..48467881,2	K562	blood:
10	chr4:48581199..48583322-chr4:48590838..48593348,2	MCF-7	breast:
11	chr4:48544834..48546523-chr4:48551748..48553430,2	K562	blood:
12	chr4:48341909..48343469-chr4:48483589..48486077,2	K562	blood:
13	chr4:48504140..48506911-chr4:48507772..48510124,3	K562	blood:
14	chr4:48510100..48513571-chr4:48516214..48518861,3	K562	blood:
15	chr4:48485093..48486693-chr4:48499386..48502011,2	K562	blood:
16	chr4:48474711..48478093-chr4:48481760..48484353,3	K562	blood:
17	chr4:48626369..48628098-chr4:48781487..48784150,2	MCF-7	breast:
18	chr4:48531467..48532998-chr4:48535012..48537828,2	K562	blood:
19	chr4:48518871..48522013-chr4:48524395..48528257,3	K562	blood:
20	chr4:48548401..48550013-chr4:48550909..48552410,2	K562	blood:
21	chr4:48533601..48535229-chr4:48537411..48540962,3	K562	blood:
22	chr4:48579352..48581122-chr4:48952741..48955150,2	K562	blood:
23	chr4:48465348..48467706-chr4:48469916..48472913,2	K562	blood:
24	chr4:48604072..48606104-chr4:48608463..48610231,2	MCF-7	breast:
25	chr4:48595665..48598613-chr4:48625026..48627031,2	K562	blood:
26	chr4:48622239..48624002-chr4:48627725..48630280,2	K562	blood:
27	chr4:48580146..48580771-chr4:48964761..48965396,2	MCF-7	breast:
28	chr4:48544834..48546523-chr4:48551748..48553430,2	K562	blood:
29	chr4:48341515..48344236-chr4:48506268..48509029,2	K562	blood:
30	chr4:48569131..48571237-chr4:48574832..48577554,2	K562	blood:
31	chr4:48566885..48569741-chr4:48570273..48573517,4	K562	blood:
32	chr4:48615973..48618309-chr4:48625425..48627835,2	K562	blood:
33	chr4:48556937..48558683-chr4:48576699..48578882,2	MCF-7	breast:
34	chr4:48592723..48596474-chr4:48596603..48599281,4	K562	blood:
35	chr4:48615973..48618309-chr4:48625425..48627835,2	K562	blood:
36	chr4:48470613..48473605-chr4:48483199..48486711,3	K562	blood:
37	chr4:48485954..48488857-chr4:48528912..48531083,2	K562	blood:
38	chr4:48484114..48487251-chr4:48504187..48509460,5	K562	blood:
39	chr4:48580560..48583320-chr4:48586437..48588078,2	K562	blood:
40	chr4:48581741..48583437-chr4:48781686..48783463,2	MCF-7	breast:
41	chr4:48478979..48481680-chr4:48482843..48484535,2	K562	blood:
42	chr4:48504789..48507033-chr4:48508012..48511920,5	K562	blood:
43	chr4:48573447..48576202-chr4:48576256..48578192,2	K562	blood:
44	chr4:48590381..48593242-chr4:48779651..48782070,2	K562	blood:
45	chr4:48590381..48593753-chr4:48779651..48782070,3	K562	blood:
46	chr4:48622239..48624002-chr4:48627725..48630280,2	K562	blood:
47	chr4:48577348..48579735-chr4:48781107..48783009,2	MCF-7	breast:
48	chr4:48633555..48635188-chr4:48638228..48640192,2	MCF-7	breast:
49	chr4:48580499..48581018-chr4:48898572..48899152,2	MCF-7	breast:
50	chr4:48609348..48611174-chr4:48646484..48649204,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-OCIAD2-3	chr4:48636435-48636507	NONHSAT096290
2	lnc-OCIAD2-3	chr4:48638867-48640580	NONHSAT096292
3	lnc-OCIAD2-3	chr4:48636435-48636507	NONHSAT096291

No data

Variant related genes	Relation type
SLC10A4	TF binding region
ZAR1	TF binding region
FRYL	TF binding region
RNU5E-3P	TF binding region
SLC10A4	CpG island
ZAR1	CpG island
FRYL	CpG island
RNU5E-3P	CpG island
ENSG00000075539	chromatin interactions
ENSG00000145248	chromatin interactions
ENSG00000109180	chromatin interactions
ENSG00000135605	chromatin interactions
ENSG00000109171	chromatin interactions
ENSG00000251722	chromatin interactions

Extended variants
information (count: 5735 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:5735 , 50 per page) page: 1 2 3 4 5 6 7 ... 115

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs531461543	chr4:48467694-48467695	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs10024547	chr4:48467710-48467711	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs563337111	chr4:48467724-48467725	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs530411073	chr4:48467734-48467735	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs549092240	chr4:48467736-48467737	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs567391942	chr4:48467737-48467738	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs534669603	chr4:48467738-48467739	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs548018359	chr4:48467744-48467745	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs561765476	chr4:48467758-48467759	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs143747343	chr4:48467796-48467797	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs558155196	chr4:48467805-48467806	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs576415905	chr4:48467859-48467860	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs112769712	chr4:48467948-48467949	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs537027642	chr4:48467951-48467952	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs34063419	chr4:48467985-48467986	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs386400017	chr4:48467990-48467991	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs386400018	chr4:48467992-48467993	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs11459953	chr4:48467996-48467997	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs555311397	chr4:48468007-48468008	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs573807984	chr4:48468014-48468015	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs541081536	chr4:48468032-48468033	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs559172742	chr4:48468072-48468073	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs577754647	chr4:48468100-48468101	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs376063968	chr4:48468109-48468110	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs371570912	chr4:48468113-48468114	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs186414367	chr4:48468136-48468137	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs548066704	chr4:48468195-48468196	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs563413396	chr4:48468200-48468201	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs566385381	chr4:48468207-48468208	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs115144205	chr4:48468251-48468252	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs533532273	chr4:48468252-48468253	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs374357455	chr4:48468258-48468259	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs549015441	chr4:48468288-48468289	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs551973635	chr4:48468304-48468305	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs189587459	chr4:48468305-48468306	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs528196951	chr4:48468320-48468321	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs143352291	chr4:48468328-48468329	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs546715562	chr4:48468342-48468343	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs572865638	chr4:48468343-48468344	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs566303753	chr4:48468355-48468356	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs539627548	chr4:48468379-48468380	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs552075889	chr4:48468380-48468381	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs570273354	chr4:48468406-48468407	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs182280059	chr4:48468556-48468557	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs186324576	chr4:48468562-48468563	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs191134433	chr4:48468573-48468574	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs534833215	chr4:48468596-48468597	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs114066667	chr4:48468611-48468612	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs577796005	chr4:48468710-48468711	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs13125379	chr4:48468746-48468747	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:64)

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
Non-syndromic sensorineural hearing loss	22037309	CNVD
Renal cell carcinoma	20952505	CNVD

Chromatin state (count:4577 , 50 per page) page: 1 2 3 4 5 6 7 ... 92

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:48464400-48471600	Weak transcription	Cortex derived primary cultured neurospheres	brain
2	chr4:48467600-48467800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr4:48467800-48468600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr4:48468600-48469800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr4:48469400-48469800	Enhancers	Brain Hippocampus Middle	brain
6	chr4:48469600-48470000	Active TSS	NHDF-Ad	bronchial
7	chr4:48469600-48470000	Enhancers	Osteobl	bone
8	chr4:48469800-48470000	Enhancers	Brain Germinal Matrix	brain
9	chr4:48469800-48471600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr4:48469800-48471600	Weak transcription	Brain Hippocampus Middle	brain
11	chr4:48470000-48470200	Enhancers	NHDF-Ad	bronchial
12	chr4:48470000-48471600	Weak transcription	Brain Germinal Matrix	brain
13	chr4:48470000-48474400	Weak transcription	Osteobl	bone
14	chr4:48471600-48472400	Enhancers	Brain Substantia Nigra	brain
15	chr4:48471600-48472600	Enhancers	Brain Hippocampus Middle	brain
16	chr4:48471600-48473000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr4:48471600-48473200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr4:48471600-48473400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr4:48471600-48473400	Enhancers	Brain Cingulate Gyrus	brain
20	chr4:48471600-48473600	Enhancers	Cortex derived primary cultured neurospheres	brain
21	chr4:48471600-48473600	Enhancers	Brain Germinal Matrix	brain
22	chr4:48471800-48472600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
23	chr4:48472200-48473000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
24	chr4:48472200-48473000	Enhancers	HSMMtube	muscle
25	chr4:48472400-48472600	Enhancers	Brain Anterior Caudate	brain
26	chr4:48472400-48473000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
27	chr4:48472400-48473000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
28	chr4:48472400-48473000	Enhancers	Muscle Satellite Cultured Cells	--
29	chr4:48472400-48473000	Flanking Active TSS	Brain Substantia Nigra	brain
30	chr4:48472400-48473200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
31	chr4:48472400-48473200	Enhancers	HSMM	muscle
32	chr4:48472600-48472800	Enhancers	Brain Inferior Temporal Lobe	brain
33	chr4:48472600-48473000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr4:48472600-48473000	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
35	chr4:48472600-48473000	Flanking Active TSS	Brain Hippocampus Middle	brain
36	chr4:48472600-48473000	Enhancers	Fetal Stomach	stomach
37	chr4:48472600-48473000	Enhancers	NH-A	brain
38	chr4:48472600-48473200	Enhancers	Brain Angular Gyrus	brain
39	chr4:48472600-48473200	Flanking Active TSS	Brain Anterior Caudate	brain
40	chr4:48472800-48473000	Enhancers	H9 Cell Line	embryonic stem cell
41	chr4:48472800-48473000	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
42	chr4:48473000-48473200	Active TSS	Brain Inferior Temporal Lobe	brain
43	chr4:48473000-48473200	Enhancers	Brain Substantia Nigra	brain
44	chr4:48473000-48473400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
45	chr4:48473000-48473400	Enhancers	Brain Hippocampus Middle	brain
46	chr4:48473000-48482000	Weak transcription	H9 Cell Line	embryonic stem cell
47	chr4:48473000-48483600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr4:48473200-48473400	Enhancers	Brain Anterior Caudate	brain
49	chr4:48473600-48479400	Weak transcription	Cortex derived primary cultured neurospheres	brain
50	chr4:48475200-48475600	Enhancers	HUES6 Cell Line	embryonic stem cell

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