Variant report

Variant	nsv470034
Chromosome Location	chr4:48427773-48605628
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1689)
CpG islands
(count:2262)
Chromatin interactive
region (count:111)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1689 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:48447770-48448033	K562	blood:	n/a	n/a
2	ARID3A	chr4:48506369-48506683	K562	blood:	n/a	n/a
3	ARID3A	chr4:48597297-48597435	K562	blood:	n/a	n/a
4	ARID3A	chr4:48593472-48593744	K562	blood:	n/a	n/a
5	ARID3A	chr4:48533201-48533219	K562	blood:	n/a	n/a
6	ARID3A	chr4:48605411-48605798	HepG2	liver:	n/a	n/a
7	ARID3A	chr4:48447705-48448039	HepG2	liver:	n/a	n/a
8	ARID3A	chr4:48484962-48485247	K562	blood:	n/a	n/a
9	ARID3A	chr4:48477763-48478047	K562	blood:	n/a	n/a
10	ARID3A	chr4:48580424-48580701	HepG2	liver:	n/a	n/a
11	ARID3A	chr4:48487020-48487153	K562	blood:	n/a	n/a
12	ARID3A	chr4:48483723-48484037	K562	blood:	n/a	n/a
13	ATF1	chr4:48483638-48483988	K562	blood:	n/a	n/a
14	ATF1	chr4:48593488-48593917	K562	blood:	n/a	n/a
15	ATF2	chr4:48501459-48502226	GM12878	blood:	n/a	n/a
16	ATF2	chr4:48501607-48502148	GM12878	blood:	n/a	n/a
17	ATF3	chr4:48578069-48578255	K562	blood:	n/a	n/a
18	ATF3	chr4:48580349-48580732	K562	blood:	n/a	n/a
19	BACH1	chr4:48486855-48487010	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr4:48493250-48493536	H1-hESC	embryonic stem cell:	n/a	n/a
21	BACH1	chr4:48520028-48520120	K562	blood:	n/a	n/a
22	BACH1	chr4:48501052-48501115	H1-hESC	embryonic stem cell:	n/a	n/a
23	BACH1	chr4:48485777-48486288	H1-hESC	embryonic stem cell:	n/a	n/a
24	BACH1	chr4:48485381-48485382	H1-hESC	embryonic stem cell:	n/a	n/a
25	BACH1	chr4:48506422-48506590	K562	blood:	n/a	n/a
26	BATF	chr4:48501720-48502070	GM12878	blood:	n/a	n/a
27	BATF	chr4:48501757-48502084	GM12878	blood:	n/a	n/a
28	BHLHE40	chr4:48477903-48478176	K562	blood:	n/a	n/a
29	BHLHE40	chr4:48501765-48502234	GM12878	blood:	n/a	n/a
30	BHLHE40	chr4:48451314-48451472	K562	blood:	n/a	n/a
31	BHLHE40	chr4:48486934-48487121	K562	blood:	n/a	n/a
32	BHLHE40	chr4:48593502-48593748	K562	blood:	n/a	n/a
33	BHLHE40	chr4:48451181-48451478	HepG2	liver:	n/a	n/a
34	BHLHE40	chr4:48485470-48485714	K562	blood:	n/a	chr4:48485560-48485576
35	BHLHE40	chr4:48483691-48483965	K562	blood:	n/a	n/a
36	CBX3	chr4:48485746-48486116	K562	blood:	n/a	n/a
37	CBX3	chr4:48483613-48484010	K562	blood:	n/a	n/a
38	CCNT2	chr4:48492468-48492539	K562	blood:	n/a	n/a
39	CCNT2	chr4:48485129-48486088	K562	blood:	n/a	n/a
40	CCNT2	chr4:48499832-48499865	K562	blood:	n/a	n/a
41	CCNT2	chr4:48483694-48483987	K562	blood:	n/a	n/a
42	CCNT2	chr4:48477848-48478194	K562	blood:	n/a	n/a
43	CCNT2	chr4:48510600-48510755	K562	blood:	n/a	n/a
44	CCNT2	chr4:48486352-48486939	K562	blood:	n/a	n/a
45	CEBPB	chr4:48449009-48449284	IMR90	lung:	n/a	chr4:48449123-48449134
46	CEBPB	chr4:48513630-48513786	K562	blood:	n/a	chr4:48513694-48513705 chr4:48513693-48513706
47	CEBPB	chr4:48548337-48548646	MCF-7	breast:	n/a	n/a
48	CEBPB	chr4:48513535-48513834	HepG2	liver:	n/a	chr4:48513694-48513705 chr4:48513693-48513706
49	CEBPB	chr4:48587083-48587650	HepG2	liver:	n/a	chr4:48587132-48587143
50	CEBPB	chr4:48580364-48580763	Hela-S3	cervix:	n/a	n/a

(count:2262 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:48492225-48492275	HAEpiC	amniotic membrane:	n/a
2	chr4:48492344-48492394	H1-hESC	embryonic stem cell:	embryo
3	chr4:48492225-48492275	MCF-7	breast:	n/a
4	chr4:48493846-48493896	GM12891	blood:	n/a
5	chr4:48431647-48431697	AG10803	skin:	n/a
6	chr4:48492225-48492275	HAEpiC	amniotic membrane:	n/a
7	chr4:48492344-48492394	H1-hESC	embryonic stem cell:	embryo
8	chr4:48492225-48492275	MCF-7	breast:	n/a
9	chr4:48493846-48493896	GM12891	blood:	n/a
10	chr4:48431647-48431697	AG10803	skin:	n/a
11	chr4:48520387-48520437	ECC-1	luminal epithelium:	n/a
12	chr4:48492304-48492354	HAEpiC	amniotic membrane:	n/a
13	chr4:48485301-48485351	T-47D	breast:	n/a
14	chr4:48491941-48491991	SAEC	small airway:	n/a
15	chr4:48485328-48485378	MCF-7	breast:	n/a
16	chr4:48493350-48493400	PrEC	prostate:	n/a
17	chr4:48501509-48501559	HIPEpiC	eye:	n/a
18	chr4:48485289-48485339	HCT-116	colon:	n/a
19	chr4:48493846-48493896	RPTEC	kidney:	n/a
20	chr4:48486472-48486522	NHDF-neo	bronchial:	n/a
21	chr4:48486785-48486835	HRCEpiC	kidney:	n/a
22	chr4:48492304-48492354	AoSMC	blood vessel:	n/a
23	chr4:48492225-48492275	PANC-1	pancreas:	n/a
24	chr4:48486472-48486522	NHBE	bronchial:	n/a
25	chr4:48486472-48486522	GM12892	blood:	n/a
26	chr4:48486785-48486835	PFSK-1	brain:	n/a
27	chr4:48501509-48501559	RPTEC	kidney:	n/a
28	chr4:48485090-48485140	SKMC	muscle:	n/a
29	chr4:48491941-48491991	HUVEC	blood vessel:	n/a
30	chr4:48520387-48520437	GM12878	blood:	n/a
31	chr4:48492344-48492394	GM12891	blood:	n/a
32	chr4:48500942-48500992	GM12878	blood:	n/a
33	chr4:48485624-48485674	LNCaP	prostate:	n/a
34	chr4:48492848-48492898	AG04450	lung:	fetal
35	chr4:48492118-48492168	AG04450	lung:	fetal
36	chr4:48491941-48491991	NHDF-neo	bronchial:	n/a
37	chr4:48485328-48485378	AoSMC	blood vessel:	n/a
38	chr4:48486316-48486366	SK-N-SH	brain:	n/a
39	chr4:48489221-48489271	HNPCEpiC	eye:	n/a
40	chr4:48492196-48492246	NH-A	brain:	n/a
41	chr4:48485293-48485343	HCT-116	colon:	n/a
42	chr4:48492118-48492168	SAEC	small airway:	n/a
43	chr4:48491941-48491991	Hepatocyte	liver:	n/a
44	chr4:48520387-48520437	SKMC	muscle:	n/a
45	chr4:48485293-48485343	LNCaP	prostate:	n/a
46	chr4:48492225-48492275	H1-hESC	embryonic stem cell:	embryo
47	chr4:48492118-48492168	HPAEpiC	pulmonary alveolar:	n/a
48	chr4:48485569-48485619	HCF	heart:	n/a
49	chr4:48485569-48485619	PANC-1	pancreas:	n/a
50	chr4:48492122-48492172	AG09319	gingival:	n/a

(count:111 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr4:48531467..48532998-chr4:48535012..48537828,2	K562	blood:
2	chr4:48173412..48176298-chr4:48428298..48430775,2	K562	blood:
3	chr4:48465348..48467706-chr4:48469916..48472913,2	K562	blood:
4	chr4:48533019..48535101-chr4:48539868..48542141,2	K562	blood:
5	chr4:48435674..48437521-chr4:48577524..48579484,2	K562	blood:
6	chr4:48549603..48551495-chr4:48553529..48555735,2	K562	blood:
7	chr4:48566885..48569741-chr4:48570273..48573517,4	K562	blood:
8	chr4:48518871..48522013-chr4:48524395..48528257,3	K562	blood:
9	chr4:48426298..48428029-chr4:48428848..48431056,2	MCF-7	breast:
10	chr4:48533601..48535229-chr4:48537411..48540962,3	K562	blood:
11	chr4:48577348..48579735-chr4:48781107..48783009,2	MCF-7	breast:
12	chr4:48593211..48596100-chr4:48831975..48834046,2	K562	blood:
13	chr4:48485954..48488857-chr4:48528912..48531083,2	K562	blood:
14	chr4:48590381..48593242-chr4:48779651..48782070,2	K562	blood:
15	chr4:48573447..48576202-chr4:48576256..48578868,3	K562	blood:
16	chr4:48474711..48478093-chr4:48481760..48484353,3	K562	blood:
17	chr4:48573447..48576202-chr4:48576256..48578868,3	K562	blood:
18	chr4:48504789..48507033-chr4:48508012..48511920,5	K562	blood:
19	chr4:48478067..48481410-chr4:48493413..48496125,3	K562	blood:
20	chr4:48462803..48464644-chr4:48465855..48467881,2	K562	blood:
21	chr4:48504140..48506911-chr4:48507772..48510124,3	K562	blood:
22	chr4:48430637..48432155-chr4:48435561..48437502,2	MCF-7	breast:
23	chr4:48456400..48458148-chr4:48459836..48461685,2	K562	blood:
24	chr4:48580560..48583320-chr4:48586437..48588078,2	K562	blood:
25	chr4:48485093..48486693-chr4:48499386..48502011,2	K562	blood:
26	chr4:48474711..48478093-chr4:48481760..48484353,3	K562	blood:
27	chr4:48548401..48550013-chr4:48550909..48552410,2	K562	blood:
28	chr4:48533601..48535229-chr4:48537411..48540962,3	K562	blood:
29	chr4:48484114..48487251-chr4:48504187..48509460,5	K562	blood:
30	chr4:48579844..48581461-chr4:48964715..48966249,12	MCF-7	breast:
31	chr4:48537925..48542072-chr4:48545238..48547735,4	MCF-7	breast:
32	chr4:48435674..48437521-chr4:48577524..48579484,2	K562	blood:
33	chr4:48527827..48530462-chr4:48535078..48536681,2	K562	blood:
34	chr4:48505446..48507840-chr4:48520996..48523756,2	K562	blood:
35	chr4:48592723..48596474-chr4:48596603..48599281,4	K562	blood:
36	chr4:48556937..48558683-chr4:48576699..48578882,2	MCF-7	breast:
37	chr4:48581199..48583322-chr4:48590838..48593348,2	MCF-7	breast:
38	chr4:48575741..48577955-chr4:48579007..48580863,2	K562	blood:
39	chr4:48506815..48509122-chr4:48514067..48516297,2	K562	blood:
40	chr4:48478979..48481680-chr4:48482843..48484535,2	K562	blood:
41	chr4:48485954..48488857-chr4:48528912..48531083,2	K562	blood:
42	chr4:48595665..48598613-chr4:48625026..48627031,2	K562	blood:
43	chr4:48576864..48578418-chr4:48583302..48585934,2	K562	blood:
44	chr4:48426298..48428029-chr4:48428848..48431056,2	MCF-7	breast:
45	chr4:48341515..48344236-chr4:48506268..48509029,2	K562	blood:
46	chr4:48473818..48475564-chr4:48478853..48480558,2	K562	blood:
47	chr4:48478979..48481680-chr4:48482843..48484535,2	K562	blood:
48	chr4:48531467..48532998-chr4:48535012..48537828,2	K562	blood:
49	chr4:48447376..48448138-chr4:48683597..48684250,2	K562	blood:
50	chr4:48508040..48510245-chr4:48529739..48531640,2	K562	blood:

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
ENSG00000251722	chromatin interactions
ENSG00000075539	chromatin interactions
ENSG00000109180	chromatin interactions
ENSG00000135605	chromatin interactions
ENSG00000109171	chromatin interactions
ENSG00000145248	chromatin interactions

Extended variants
information (count: 5643 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:5643 , 50 per page) page: 1 2 3 4 5 6 7 ... 113

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1055721	chr4:48427773-48427774	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs556628744	chr4:48427796-48427797	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs370383127	chr4:48427800-48427801	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs374390364	chr4:48427877-48427878	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs371865042	chr4:48427928-48427929	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs532110017	chr4:48427952-48427953	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs535489598	chr4:48427957-48427958	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs554100833	chr4:48427976-48427977	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs533748155	chr4:48427988-48427989	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs572592523	chr4:48427990-48427991	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs114495443	chr4:48427991-48427992	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs548557792	chr4:48428024-48428025	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs367612802	chr4:48428026-48428027	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs190253563	chr4:48428090-48428091	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs543557551	chr4:48428092-48428093	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs75038306	chr4:48428101-48428102	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs181463903	chr4:48428102-48428103	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs529154335	chr4:48428122-48428123	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs186937013	chr4:48428153-48428154	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs191778089	chr4:48428162-48428163	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs549721524	chr4:48428163-48428164	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs532748479	chr4:48428254-48428255	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs551098734	chr4:48428284-48428285	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs57931446	chr4:48428289-48428290	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs531790364	chr4:48428320-48428321	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs56891372	chr4:48428323-48428324	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs79695301	chr4:48428329-48428330	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs536118113	chr4:48428384-48428385	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs62309454	chr4:48428394-48428395	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs150638743	chr4:48428441-48428442	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs566119980	chr4:48428562-48428563	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs539840139	chr4:48428563-48428564	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs566172544	chr4:48428607-48428608	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs558287044	chr4:48428615-48428616	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs576566027	chr4:48428624-48428625	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs183972570	chr4:48428657-48428658	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs577106775	chr4:48428698-48428699	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs555511858	chr4:48428712-48428713	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs573734648	chr4:48428726-48428727	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs541353784	chr4:48428781-48428782	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs188914708	chr4:48428826-48428827	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs139720948	chr4:48428827-48428828	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs544544901	chr4:48428845-48428846	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs189593248	chr4:48428862-48428863	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs559237345	chr4:48428876-48428877	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs556334462	chr4:48428889-48428890	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs574927762	chr4:48428908-48428909	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs550128653	chr4:48428934-48428935	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs182278961	chr4:48428960-48428961	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs375450124	chr4:48429031-48429032	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	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
Renal cell carcinoma	20952505	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:4050 , 50 per page) page: 1 2 3 4 5 6 7 ... 81

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:48382200-48431800	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr4:48387600-48431400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
3	chr4:48391600-48434000	Weak transcription	Fetal Heart	heart
4	chr4:48400000-48431000	Weak transcription	Brain Angular Gyrus	brain
5	chr4:48406200-48433200	Weak transcription	NHEK	skin
6	chr4:48413200-48430000	Weak transcription	Aorta	Aorta
7	chr4:48413200-48431800	Weak transcription	Brain Substantia Nigra	brain
8	chr4:48413400-48431600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
9	chr4:48421000-48428400	Strong transcription	Primary T helper cells fromperipheralblood	blood
10	chr4:48421800-48428000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
11	chr4:48421800-48429400	Weak transcription	Pancreatic Islets	Pancreatic Islet
12	chr4:48422600-48431600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr4:48422600-48432000	Weak transcription	Psoas Muscle	Psoas
14	chr4:48422600-48433200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr4:48422600-48433600	Weak transcription	Esophagus	oesophagus
16	chr4:48422600-48434400	Weak transcription	Brain Germinal Matrix	brain
17	chr4:48423200-48433200	Weak transcription	Gastric	stomach
18	chr4:48423400-48438200	Weak transcription	Fetal Intestine Small	intestine
19	chr4:48423600-48428000	Strong transcription	HSMM	muscle
20	chr4:48423600-48433200	Weak transcription	Pancreas	Pancrea
21	chr4:48424400-48430200	Weak transcription	Fetal Stomach	stomach
22	chr4:48424400-48432200	Weak transcription	Brain Hippocampus Middle	brain
23	chr4:48424400-48432400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
24	chr4:48424600-48432000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
25	chr4:48424800-48430400	Weak transcription	Colonic Mucosa	Colon
26	chr4:48425000-48429000	Weak transcription	Fetal Muscle Trunk	muscle
27	chr4:48425000-48431000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
28	chr4:48425000-48431600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr4:48425000-48431800	Weak transcription	GM12878-XiMat	blood
30	chr4:48425000-48433200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
31	chr4:48425200-48429200	Weak transcription	Fetal Brain Female	brain
32	chr4:48425200-48429200	Weak transcription	Fetal Muscle Leg	muscle
33	chr4:48425200-48430000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
34	chr4:48425200-48431000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
35	chr4:48425200-48432000	Weak transcription	Brain Cingulate Gyrus	brain
36	chr4:48425200-48432600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
37	chr4:48425200-48433000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
38	chr4:48425200-48433200	Weak transcription	HUVEC	blood vessel
39	chr4:48425200-48433800	Weak transcription	Stomach Mucosa	stomach
40	chr4:48425200-48441600	Weak transcription	HUES6 Cell Line	embryonic stem cell
41	chr4:48425400-48429000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr4:48425400-48431000	Weak transcription	Fetal Kidney	kidney
43	chr4:48425400-48433200	Weak transcription	Placenta Amnion	Placenta Amnion
44	chr4:48425400-48438400	Weak transcription	HSMMtube	muscle
45	chr4:48425600-48431800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
46	chr4:48425600-48432800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
47	chr4:48425800-48428600	Weak transcription	Primary T cells fromperipheralblood	blood
48	chr4:48425800-48429200	Weak transcription	Brain Inferior Temporal Lobe	brain
49	chr4:48425800-48429200	Weak transcription	Colon Smooth Muscle	Colon
50	chr4:48425800-48429400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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