Variant report

Variant	esv1792557
Chromosome Location	chr4:94738158-95027272
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1023)
CpG islands
(count:1652)
Chromatin interactive
region (count:26)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1023 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:94997726-94997899	K562	blood:	n/a	n/a
2	ARID3A	chr4:94997397-94997461	K562	blood:	n/a	n/a
3	ARID3A	chr4:94818851-94819083	K562	blood:	n/a	n/a
4	ATF2	chr4:94755543-94755979	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr4:94755618-94756055	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr4:94868527-94868591	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr4:94749609-94750066	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr4:94750340-94750341	H1-hESC	embryonic stem cell:	n/a	n/a
9	BATF	chr4:94801131-94801367	GM12878	blood:	n/a	n/a
10	BATF	chr4:94958134-94958453	GM12878	blood:	n/a	chr4:94958333-94958343 chr4:94958332-94958343
11	BCL11A	chr4:94801154-94801387	GM12878	blood:	n/a	n/a
12	BCL11A	chr4:94868552-94868745	H1-hESC	embryonic stem cell:	n/a	n/a
13	BCL3	chr4:94794718-94794972	GM12878	blood:	n/a	n/a
14	BCL3	chr4:94794603-94795001	GM12878	blood:	n/a	n/a
15	BHLHE40	chr4:94749781-94749934	GM12878	blood:	n/a	n/a
16	BHLHE40	chr4:94749723-94749891	HepG2	liver:	n/a	n/a
17	BHLHE40	chr4:94876941-94876943	GM12878	blood:	n/a	n/a
18	BHLHE40	chr4:94749717-94750001	K562	blood:	n/a	n/a
19	BRCA1	chr4:94905803-94906175	GM12878	blood:	n/a	n/a
20	BRCA1	chr4:94910844-94910885	GM12878	blood:	n/a	n/a
21	BRCA1	chr4:94846230-94846320	H1-hESC	embryonic stem cell:	n/a	n/a
22	CCNT2	chr4:94932469-94932662	K562	blood:	n/a	n/a
23	CCNT2	chr4:94994591-94994708	K562	blood:	n/a	n/a
24	CCNT2	chr4:94750064-94750261	K562	blood:	n/a	n/a
25	CEBPB	chr4:94756157-94756414	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr4:94757411-94757742	IMR90	lung:	n/a	n/a
27	CEBPB	chr4:94891026-94891291	HepG2	liver:	n/a	chr4:94891149-94891160
28	CEBPB	chr4:94926475-94926745	HepG2	liver:	n/a	chr4:94926595-94926606
29	CEBPB	chr4:94873940-94874155	HepG2	liver:	n/a	n/a
30	CEBPB	chr4:94827807-94828222	K562	blood:	n/a	chr4:94828078-94828089
31	CEBPB	chr4:94749441-94749677	H1-hESC	embryonic stem cell:	n/a	n/a
32	CEBPB	chr4:94871501-94871665	A549	lung:	n/a	n/a
33	CEBPB	chr4:94992196-94992612	IMR90	lung:	n/a	chr4:94992297-94992308
34	CEBPB	chr4:94827811-94828196	IMR90	lung:	n/a	chr4:94828078-94828089
35	CEBPB	chr4:94871470-94871731	K562	blood:	n/a	n/a
36	CEBPB	chr4:95026371-95026478	H1-hESC	embryonic stem cell:	n/a	n/a
37	CEBPB	chr4:94992171-94992463	A549	lung:	n/a	chr4:94992297-94992308
38	CEBPB	chr4:94800063-94800263	A549	lung:	n/a	n/a
39	CEBPB	chr4:95026418-95026482	HepG2	liver:	n/a	n/a
40	CEBPB	chr4:94990640-94990820	A549	lung:	n/a	n/a
41	CEBPB	chr4:94827913-94828113	H1-hESC	embryonic stem cell:	n/a	chr4:94828078-94828089
42	CEBPB	chr4:95019171-95019220	H1-hESC	embryonic stem cell:	n/a	n/a
43	CEBPB	chr4:94871526-94871743	MCF-7	breast:	n/a	n/a
44	CEBPB	chr4:94992170-94992533	HepG2	liver:	n/a	chr4:94992297-94992308
45	CEBPB	chr4:94936002-94936234	HepG2	liver:	n/a	chr4:94936070-94936081
46	CEBPB	chr4:94827888-94828183	HepG2	liver:	n/a	chr4:94828078-94828089
47	CEBPB	chr4:94992228-94992503	Hela-S3	cervix:	n/a	chr4:94992297-94992308
48	CEBPB	chr4:95026372-95026492	K562	blood:	n/a	n/a
49	CEBPB	chr4:94824863-94825171	H1-hESC	embryonic stem cell:	n/a	n/a
50	CEBPB	chr4:94990618-94990908	H1-hESC	embryonic stem cell:	n/a	n/a

(count:1652 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:94748860-94748910	BE2_C	brain:	n/a
2	chr4:94749890-94749940	CMK	blood:	n/a
3	chr4:94750205-94750255	HUVEC	blood vessel:	n/a
4	chr4:94746669-94746719	ECC-1	luminal epithelium:	n/a
5	chr4:94748686-94748736	AG09319	gingival:	n/a
6	chr4:94748860-94748910	BE2_C	brain:	n/a
7	chr4:94749890-94749940	CMK	blood:	n/a
8	chr4:94750205-94750255	HUVEC	blood vessel:	n/a
9	chr4:94746669-94746719	ECC-1	luminal epithelium:	n/a
10	chr4:94748686-94748736	AG09319	gingival:	n/a
11	chr4:94748686-94748736	NB4	blood:	n/a
12	chr4:94750047-94750097	BJ	skin:	n/a
13	chr4:94756031-94756081	U87	brain:	n/a
14	chr4:94759825-94759875	AG10803	skin:	n/a
15	chr4:94750997-94751047	GM06990	blood:	n/a
16	chr4:94748686-94748736	MCF10A-Er-Src	breast:	n/a
17	chr4:94753403-94753453	NHBE	bronchial:	n/a
18	chr4:94755520-94755570	CMK	blood:	n/a
19	chr4:94753403-94753453	HEEpiC	esophagus:	n/a
20	chr4:94748617-94748667	SK-N-SH_RA	brain:	n/a
21	chr4:94750997-94751047	ovcar-3	ovarian:	n/a
22	chr4:94759825-94759875	GM12892	blood:	n/a
23	chr4:94755787-94755837	BE2_C	brain:	n/a
24	chr4:94749865-94749915	SAEC	small airway:	n/a
25	chr4:94751126-94751176	NT2-D1	testis:	n/a
26	chr4:94756031-94756081	MCF-7	breast:	n/a
27	chr4:94753431-94753481	Jurkat	blood:	n/a
28	chr4:94748860-94748910	NH-A	brain:	n/a
29	chr4:94749890-94749940	PrEC	prostate:	n/a
30	chr4:94749535-94749585	Hepatocyte	liver:	n/a
31	chr4:94748686-94748736	HRPEpiC	eye:	n/a
32	chr4:94749865-94749915	NT2-D1	testis:	n/a
33	chr4:94748617-94748667	T-47D	breast:	n/a
34	chr4:94755787-94755837	GM12878	blood:	n/a
35	chr4:94749496-94749546	Hepatocyte	liver:	n/a
36	chr4:94750205-94750255	NHBE	bronchial:	n/a
37	chr4:94881257-94881307	RPTEC	kidney:	n/a
38	chr4:94749496-94749546	HepG2	liver:	n/a
39	chr4:94751126-94751176	HCF	heart:	n/a
40	chr4:94759825-94759875	HEK293	kidney:	embryo
41	chr4:94759825-94759875	MCF-7	breast:	n/a
42	chr4:94748860-94748910	ovcar-3	ovarian:	n/a
43	chr4:94750997-94751047	HNPCEpiC	eye:	n/a
44	chr4:94749609-94749659	HRE	kidney:	n/a
45	chr4:94748619-94748669	MCF-7	breast:	n/a
46	chr4:94756895-94756945	SAEC	small airway:	n/a
47	chr4:94753431-94753481	HL-60	blood:	n/a
48	chr4:94755787-94755837	HRE	kidney:	n/a
49	chr4:94749535-94749585	GM06990	blood:	n/a
50	chr4:94753431-94753481	BJ	skin:	n/a

(count:26 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:94983452..94985612-chr4:94998782..95000432,2	K562	blood:
2	chr4:94822596..94823096-chr5:81267395..81268373,2	NB4	blood:
3	chr10:108384719..108385233-chr4:94854360..94855166,2	MCF-7	breast:
4	chr4:94760735..94763109-chr4:95132947..95134725,2	K562	blood:
5	chr4:94984924..94988531-chr4:94994080..94995912,3	K562	blood:
6	chr4:94748371..94749981-chr4:94756067..94758065,2	K562	blood:
7	chr4:94931645..94934547-chr4:94969547..94971822,2	K562	blood:
8	chr4:94786106..94788716-chr4:95078426..95081132,2	K562	blood:
9	chr4:94984924..94987149-chr4:94994387..94995912,2	K562	blood:
10	chr4:94983452..94985612-chr4:94998782..95000432,2	K562	blood:
11	chr4:94900894..94903042-chr4:94911254..94913971,2	K562	blood:
12	chr4:94809463..94811409-chr4:94820137..94822795,2	K562	blood:
13	chr4:94931645..94934547-chr4:94969547..94971822,2	K562	blood:
14	chr4:94900894..94903042-chr4:94911254..94913971,2	K562	blood:
15	chr4:94818194..94819480-chr4:95047856..95049178,6	MCF-7	breast:
16	chr4:94902454..94905004-chr4:94999275..95001827,2	K562	blood:
17	chr4:94818426..94818969-chr4:95048490..95049106,2	K562	blood:
18	chr4:94984924..94988531-chr4:94994080..94995912,3	K562	blood:
19	chr4:94748189..94750312-chr4:94760704..94763449,2	MCF-7	breast:
20	chr4:94748371..94749981-chr4:94756067..94758065,2	K562	blood:
21	chr4:94979077..94981724-chr4:94984973..94987094,2	K562	blood:
22	chr4:94979077..94981724-chr4:94984973..94987094,2	K562	blood:
23	chr4:94984924..94987149-chr4:94994387..94995912,2	K562	blood:
24	chr4:94809463..94811409-chr4:94820137..94822795,2	K562	blood:
25	chr4:94834970..94836520-chr4:95108822..95111523,2	K562	blood:
26	chr4:94902454..94905004-chr4:94999275..95001827,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SMARCAD1-2	chr4:95010890-95010920	NONHSAT097440
2	lnc-SMARCAD1-2	chr4:95008196-95008609	NONHSAT097440
3	lnc-SMARCAD1-2	chr4:95007501-95007629	NONHSAT097440

No data

Variant related genes	Relation type
RNA5SP164	TF binding region
ATOH1	TF binding region
RNA5SP164	CpG island
ATOH1	CpG island
ENSG00000152348	chromatin interactions
ENSG00000172238	chromatin interactions

Extended variants
information (count: 5391 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:5391 , 50 per page) page: 1 2 3 4 5 6 7 ... 108

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs113373839	chr4:94738776-94738777	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs181037059	chr4:94738839-94738840	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs531833742	chr4:94738840-94738841	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs551918141	chr4:94738842-94738843	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs4693345	chr4:94738890-94738891	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs78868966	chr4:94744412-94744413	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs374033080	chr4:94744449-94744450	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs112514844	chr4:94744467-94744468	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs369749097	chr4:94744469-94744470	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs368560883	chr4:94744509-94744510	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs564467515	chr4:94744561-94744562	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs201681822	chr4:94744568-94744569	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs59071973	chr4:94744599-94744600	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs534845319	chr4:94745226-94745227	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
15	rs556277885	chr4:94745239-94745240	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
16	rs185480090	chr4:94745284-94745285	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
17	rs538923439	chr4:94745313-94745314	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
18	rs558215320	chr4:94745316-94745317	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
19	rs578054097	chr4:94745320-94745321	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
20	rs540598830	chr4:94745328-94745329	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
21	rs527262824	chr4:94745356-94745357	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
22	rs560393451	chr4:94745372-94745373	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
23	rs574034039	chr4:94745394-94745395	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
24	rs187954657	chr4:94745404-94745405	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs542902162	chr4:94745453-94745454	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs192838065	chr4:94745475-94745476	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs6850864	chr4:94745479-94745480	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs551637374	chr4:94745480-94745481	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs565209243	chr4:94745486-94745487	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs530060686	chr4:94745522-94745523	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs11731687	chr4:94745528-94745529	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs546947802	chr4:94745532-94745533	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs567252468	chr4:94745533-94745534	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs138725049	chr4:94745543-94745544	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs368381036	chr4:94745583-94745584	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs80259728	chr4:94745587-94745588	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs371947964	chr4:94745674-94745675	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs569814729	chr4:94745737-94745738	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs538961717	chr4:94745755-94745756	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs558908424	chr4:94745758-94745759	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs565941817	chr4:94745762-94745763	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs6532435	chr4:94745800-94745801	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs564425159	chr4:94745814-94745815	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs548277306	chr4:94745816-94745817	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs184854701	chr4:94745827-94745828	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs543092005	chr4:94745843-94745844	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs556508681	chr4:94745879-94745880	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs74893239	chr4:94745899-94745900	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs143962639	chr4:94745924-94745925	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs565245693	chr4:94745928-94745929	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:90)

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
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
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Parkinson disease	18923514	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Breast cancer	16272173	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
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelodysplastic syndrome	21251322	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	18414403	CNVD
primary effusion lymphomas	17116491	CNVD
Mental retardation	20522426	CNVD
delayed speech	20522426	CNVD
growth disorder	20522426	CNVD
small cell lung cancer	20016488	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Colorectal cancer	20459617	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Hirschsprung''s Disease	21712996	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Breast cancer	17393978	CNVD
Ovarian cancer	21720365	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Esophageal cancer	21851588	CNVD
Cancer	19907438	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Prostate cancer	16573809	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Epilepsy	20502679	CNVD
Glioma	20126413	CNVD
early-passage human iPS cells	21368824	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Sinonasal adenocarcinoma	21360264	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:828 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:94744400-94744600	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
2	chr4:94745200-94745400	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr4:94745400-94748800	Weak transcription	Pancreas	Pancrea
4	chr4:94746200-94746400	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr4:94746800-94747200	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
6	chr4:94746800-94748200	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
7	chr4:94747000-94747200	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
8	chr4:94747000-94748200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
9	chr4:94747200-94748200	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
10	chr4:94747800-94748200	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
11	chr4:94748000-94748400	Flanking Bivalent TSS/Enh	HUES64 Cell Line	embryonic stem cell
12	chr4:94748000-94748600	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell
13	chr4:94748000-94749000	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
14	chr4:94748200-94748400	Flanking Bivalent TSS/Enh	ES-I3 Cell Line	embryonic stem cell
15	chr4:94748200-94748400	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
16	chr4:94748200-94748400	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell
17	chr4:94748200-94748400	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
18	chr4:94748200-94748400	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
19	chr4:94748200-94748400	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
20	chr4:94748200-94748400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
21	chr4:94748200-94748600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr4:94748200-94748600	Flanking Bivalent TSS/Enh	Rectal Mucosa Donor 31	rectum
23	chr4:94748200-94748800	Bivalent Enhancer	Fetal Intestine Small	intestine
24	chr4:94748200-94748800	Bivalent Enhancer	NHEK	skin
25	chr4:94748200-94749200	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr4:94748200-94749400	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
27	chr4:94748400-94748600	Flanking Bivalent TSS/Enh	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr4:94748400-94748600	Flanking Bivalent TSS/Enh	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr4:94748400-94748600	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
30	chr4:94748400-94748600	Bivalent/Poised TSS	iPS DF 6.9 Cell Line	embryonic stem cell
31	chr4:94748400-94748600	Bivalent Enhancer	Ganglion Eminence derived primary cultured neurospheres	brain
32	chr4:94748400-94748600	Bivalent/Poised TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
33	chr4:94748400-94748600	Bivalent/Poised TSS	Brain Hippocampus Middle	brain
34	chr4:94748400-94748600	Bivalent Enhancer	Psoas Muscle	Psoas
35	chr4:94748400-94748800	Bivalent/Poised TSS	Duodenum Mucosa	Duodenum
36	chr4:94748400-94748800	Bivalent Enhancer	Esophagus	oesophagus
37	chr4:94748400-94748800	Bivalent Enhancer	Fetal Intestine Large	intestine
38	chr4:94748400-94749000	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
39	chr4:94748400-94749000	Flanking Bivalent TSS/Enh	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr4:94748400-94749000	Bivalent Enhancer	Brain Germinal Matrix	brain
41	chr4:94748400-94749200	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
42	chr4:94748400-94749200	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
43	chr4:94748400-94749200	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
44	chr4:94748400-94749200	Bivalent Enhancer	Colon Smooth Muscle	Colon
45	chr4:94748400-94749200	Bivalent Enhancer	Ovary	ovary
46	chr4:94748400-94749400	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr4:94748400-94749400	Bivalent Enhancer	Adipose Nuclei	Adipose
48	chr4:94748400-94749400	Bivalent Enhancer	Brain Dorsolateral Prefrontal Cortex	brain
49	chr4:94748400-94749400	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
50	chr4:94748400-94749400	Bivalent Enhancer	Fetal Brain Female	brain

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