Variant report

Variant	nsv594915
Chromosome Location	chr4:96628653-97086618
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	ATF2	chr4:96937695-96938178	GM12878	blood:	n/a	n/a
2	BACH1	chr4:96756891-96757056	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr4:96862615-96862654	H1-hESC	embryonic stem cell:	n/a	n/a
4	BATF	chr4:96937804-96938102	GM12878	blood:	n/a	chr4:96937940-96937951
5	BATF	chr4:96937746-96938101	GM12878	blood:	n/a	chr4:96937940-96937951
6	BCL11A	chr4:96720077-96720233	H1-hESC	embryonic stem cell:	n/a	n/a
7	BCL11A	chr4:96720028-96720203	H1-hESC	embryonic stem cell:	n/a	n/a
8	BCL11A	chr4:96906479-96906682	GM12878	blood:	n/a	n/a
9	BHLHE40	chr4:96878378-96878476	GM12878	blood:	n/a	n/a
10	BRCA1	chr4:96833916-96833938	Hela-S3	cervix:	n/a	n/a
11	CBX3	chr4:96789068-96789369	HCT-116	colon:	n/a	n/a
12	CBX3	chr4:96789036-96789470	HCT-116	colon:	n/a	n/a
13	CBX3	chr4:96789054-96789386	K562	blood:	n/a	n/a
14	CBX3	chr4:96847445-96847700	K562	blood:	n/a	n/a
15	CEBPB	chr4:96969969-96970250	HepG2	liver:	n/a	chr4:96970090-96970101 chr4:96970052-96970063
16	CEBPB	chr4:96636962-96637451	ECC-1	luminal epithelium:	n/a	n/a
17	CEBPB	chr4:96668531-96669056	MCF-7	breast:	n/a	chr4:96669001-96669014
18	CEBPB	chr4:96703580-96703990	A549	lung:	n/a	chr4:96703699-96703710 chr4:96703701-96703710
19	CEBPB	chr4:96809244-96809518	IMR90	lung:	n/a	chr4:96809374-96809385
20	CEBPB	chr4:96703619-96704039	IMR90	lung:	n/a	chr4:96703699-96703710 chr4:96703701-96703710 chr4:96704005-96704016
21	CEBPB	chr4:96702017-96702218	HepG2	liver:	n/a	n/a
22	CEBPB	chr4:96668490-96669010	MCF-7	breast:	n/a	n/a
23	CEBPB	chr4:96703659-96703859	K562	blood:	n/a	chr4:96703699-96703710 chr4:96703701-96703710
24	CEBPB	chr4:96693254-96693466	HepG2	liver:	n/a	chr4:96693362-96693373
25	CEBPB	chr4:96926721-96926996	K562	blood:	n/a	chr4:96926871-96926882
26	CEBPB	chr4:96891499-96892083	HepG2	liver:	n/a	chr4:96891581-96891594 chr4:96891934-96891945
27	CEBPB	chr4:97058408-97058689	HepG2	liver:	n/a	chr4:97058529-97058540 chr4:97058530-97058541
28	CEBPB	chr4:96653308-96653672	ECC-1	luminal epithelium:	n/a	n/a
29	CEBPB	chr4:97058473-97058673	A549	lung:	n/a	chr4:97058529-97058540 chr4:97058530-97058541
30	CEBPB	chr4:96703666-96703970	HepG2	liver:	n/a	chr4:96703699-96703710 chr4:96703701-96703710
31	CEBPB	chr4:97071933-97071937	K562	blood:	n/a	n/a
32	CEBPB	chr4:96926699-96927041	HepG2	liver:	n/a	chr4:96926871-96926882
33	CEBPB	chr4:96932580-96932692	HepG2	liver:	n/a	chr4:96932600-96932613 chr4:96932600-96932611
34	CEBPB	chr4:96636890-96637488	MCF-7	breast:	n/a	n/a
35	CEBPB	chr4:97032385-97032659	Hela-S3	cervix:	n/a	n/a
36	CEBPB	chr4:96891924-96892033	H1-hESC	embryonic stem cell:	n/a	chr4:96891934-96891945
37	CEBPB	chr4:96702036-96702236	H1-hESC	embryonic stem cell:	n/a	n/a
38	CEBPB	chr4:96887445-96887558	A549	lung:	n/a	n/a
39	CEBPB	chr4:96702003-96702220	A549	lung:	n/a	n/a
40	CEBPB	chr4:96926699-96927027	IMR90	lung:	n/a	chr4:96926871-96926882
41	CEBPB	chr4:96693229-96693518	IMR90	lung:	n/a	chr4:96693362-96693373
42	CEBPB	chr4:96781173-96781373	HepG2	liver:	n/a	chr4:96781272-96781281 chr4:96781270-96781281 chr4:96781272-96781281 chr4:96781270-96781283 chr4:96781270-96781283 chr4:96781272-96781281 chr4:96781272-96781281 chr4:96781272-96781283 chr4:96781272-96781283
43	CEBPB	chr4:96871169-96871369	A549	lung:	n/a	n/a
44	CEBPB	chr4:96649188-96649501	A549	lung:	n/a	chr4:96649277-96649288 chr4:96649328-96649339
45	CEBPB	chr4:96926696-96927033	A549	lung:	n/a	chr4:96926871-96926882
46	CEBPB	chr4:96911085-96911139	K562	blood:	n/a	n/a
47	CEBPB	chr4:96888762-96889056	HepG2	liver:	n/a	chr4:96888917-96888928
48	CEBPB	chr4:96891500-96892082	IMR90	lung:	n/a	chr4:96891581-96891594 chr4:96891934-96891945
49	CEBPB	chr4:96809307-96809514	HepG2	liver:	n/a	chr4:96809374-96809385
50	CEBPB	chr4:96910953-96911234	IMR90	lung:	n/a	chr4:96911071-96911082

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:96761026-96761076	AG10803	skin:	n/a
2	chr4:96761598-96761648	AoSMC	blood vessel:	n/a
3	chr4:96761135-96761185	AG04449	skin:	fetal
4	chr4:96761231-96761281	HEK293	kidney:	embryo
5	chr4:96761796-96761846	BJ	skin:	n/a
6	chr4:96761229-96761279	RPTEC	kidney:	n/a
7	chr4:96678053-96678103	K562	blood:	n/a
8	chr4:96761026-96761076	MCF10A-Er-Src	breast:	n/a
9	chr4:97047181-97047231	Hepatocyte	liver:	n/a
10	chr4:96761231-96761281	GM12892	blood:	n/a
11	chr4:96760945-96760995	AG10803	skin:	n/a
12	chr4:96761796-96761846	HPAEpiC	pulmonary alveolar:	n/a
13	chr4:96761559-96761609	BE2_C	brain:	n/a
14	chr4:96760014-96760064	HCM	heart:	n/a
15	chr4:96836082-96836132	RPTEC	kidney:	n/a
16	chr4:96761796-96761846	SAEC	small airway:	n/a
17	chr4:97047512-97047562	GM12878	blood:	n/a
18	chr4:97047512-97047562	A549	lung:	n/a
19	chr4:96678053-96678103	HCPEpiC	choroid plexus:	n/a
20	chr4:96761229-96761279	MCF-7	breast:	n/a
21	chr4:96761796-96761846	NH-A	brain:	n/a
22	chr4:96761264-96761314	ECC-1	luminal epithelium:	n/a
23	chr4:96761559-96761609	HCT-116	colon:	n/a
24	chr4:96761377-96761427	AG09309	skin:	n/a
25	chr4:96761135-96761185	HEEpiC	esophagus:	n/a
26	chr4:97047181-97047231	PrEC	prostate:	n/a
27	chr4:96761377-96761427	ovcar-3	ovarian:	n/a
28	chr4:96761264-96761314	HNPCEpiC	eye:	n/a
29	chr4:96761377-96761427	HCM	heart:	n/a
30	chr4:96761559-96761609	AG10803	skin:	n/a
31	chr4:96761559-96761609	SK-N-MC	brain:	n/a
32	chr4:96761559-96761609	HIPEpiC	eye:	n/a
33	chr4:96761135-96761185	AG09309	skin:	n/a
34	chr4:96760014-96760064	AG09319	gingival:	n/a
35	chr4:96760945-96760995	GM12892	blood:	n/a
36	chr4:96836082-96836132	AG09319	gingival:	n/a
37	chr4:96836082-96836132	HUVEC	blood vessel:	n/a
38	chr4:96760014-96760064	AG09309	skin:	n/a
39	chr4:96761135-96761185	SK-N-SH_RA	brain:	n/a
40	chr4:96760014-96760064	U87	brain:	n/a
41	chr4:96761231-96761281	HIPEpiC	eye:	n/a
42	chr4:96760945-96760995	AG09319	gingival:	n/a
43	chr4:97047181-97047231	BE2_C	brain:	n/a
44	chr4:96761231-96761281	T-47D	breast:	n/a
45	chr4:96760945-96760995	HEK293	kidney:	embryo
46	chr4:96761264-96761314	AG09319	gingival:	n/a
47	chr4:96761229-96761279	Jurkat	blood:	n/a
48	chr4:96760014-96760064	GM12891	blood:	n/a
49	chr4:96761026-96761076	AG09319	gingival:	n/a
50	chr4:96761559-96761609	SK-N-SH	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:97080339..97083190-chr4:97083678..97085424,2	K562	blood:
2	chr4:96756581..96757503-chr4:96956588..96957342,2	MCF-7	breast:
3	chr4:97003956..97004522-chr4:97272708..97273630,2	MCF-7	breast:
4	chr4:97080339..97083190-chr4:97083678..97085424,2	K562	blood:
5	chr4:97075485..97077606-chr4:97078674..97081310,2	K562	blood:
6	chr4:97075485..97077606-chr4:97078674..97081310,2	K562	blood:
7	chr4:96669276..96670825-chr4:96677264..96679662,2	MCF-7	breast:
8	chr4:97015932..97018405-chr4:97024255..97026291,2	MCF-7	breast:
9	chr4:96749923..96752182-chr4:96773061..96775566,2	K562	blood:
10	chr4:96822970..96824843-chr4:96830954..96833894,2	K562	blood:
11	chr4:96822970..96824843-chr4:96830954..96833894,2	K562	blood:
12	chr4:96993810..96996536-chr4:96998099..97000310,2	MCF-7	breast:
13	chr4:96964832..96967791-chr4:96969895..96971458,2	K562	blood:
14	chr4:96720160..96722789-chr4:96726350..96727999,2	K562	blood:
15	chr4:96964832..96967791-chr4:96969895..96971458,2	K562	blood:
16	chr4:96749923..96752182-chr4:96773061..96775566,2	K562	blood:
17	chr4:96720160..96722789-chr4:96726350..96727999,2	K562	blood:
18	chr4:96756581..96757503-chr4:96956588..96957342,2	MCF-7	breast:
19	chr4:96669276..96670825-chr4:96677264..96679662,2	MCF-7	breast:
20	chr4:97015932..97018405-chr4:97024255..97026291,2	MCF-7	breast:
21	chr4:96674646..96677370-chr4:96678560..96681527,2	MCF-7	breast:
22	chr4:96674646..96677370-chr4:96678560..96681527,2	MCF-7	breast:
23	chr4:96817765..96820012-chr4:96825569..96827518,2	K562	blood:
24	chr4:96817765..96820012-chr4:96825569..96827518,2	K562	blood:
25	chr4:96993810..96996536-chr4:96998099..97000310,2	MCF-7	breast:

Variant related genes	Relation type
RNU6-1059P	TF binding region
PDHA2	TF binding region
RNU6-34P	TF binding region
RNU6-1059P	CpG island
PDHA2	CpG island
RNU6-34P	CpG island

Extended variants
information (count: 9447 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:9447 , 50 per page) page: 1 2 3 4 5 6 7 ... 189

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1370004	chr4:96628653-96628654	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs568769789	chr4:96628692-96628693	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs537749300	chr4:96628693-96628694	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs190897984	chr4:96628717-96628718	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs547129248	chr4:96628721-96628722	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs1370003	chr4:96628744-96628745	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs34078728	chr4:96628759-96628760	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs183924914	chr4:96628769-96628770	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs1370002	chr4:96628781-96628782	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs3040611	chr4:96628816-96628817	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs60429533	chr4:96628818-96628819	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs573700314	chr4:96628833-96628834	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs542612298	chr4:96628911-96628912	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs556204800	chr4:96628918-96628919	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs188874191	chr4:96628937-96628938	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs544918929	chr4:96628978-96628979	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs199737746	chr4:96629047-96629048	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs397745205	chr4:96629050-96629051	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs397950311	chr4:96629051-96629052	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs386677484	chr4:96629070-96629071	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs115459649	chr4:96629071-96629072	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs576543156	chr4:96629080-96629081	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs192341517	chr4:96629142-96629143	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs183013797	chr4:96629176-96629177	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs376717226	chr4:96629190-96629191	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs187308323	chr4:96629194-96629195	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs1865851	chr4:96629200-96629201	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs575013427	chr4:96632808-96632809	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs187600070	chr4:96632816-96632817	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs142613119	chr4:96632831-96632832	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs532992620	chr4:96632876-96632877	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs552576497	chr4:96632883-96632884	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs560113821	chr4:96632913-96632914	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs190513884	chr4:96632932-96632933	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs548813537	chr4:96632981-96632982	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs568525106	chr4:96632994-96632995	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs557401665	chr4:96633001-96633002	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs117492880	chr4:96633002-96633003	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs183052880	chr4:96633005-96633006	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs553666538	chr4:96633014-96633015	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs570747823	chr4:96633028-96633029	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs575966533	chr4:96633069-96633070	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs113900096	chr4:96633081-96633082	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs375013418	chr4:96633099-96633100	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs552972377	chr4:96633100-96633101	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs111675937	chr4:96633116-96633117	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs377664886	chr4:96633165-96633166	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs555153635	chr4:96633236-96633237	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs12449054	chr4:96633251-96633252	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs139886706	chr4:96633273-96633274	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:85)

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
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
Prostate cancer	16573809	CNVD
Multiple myeloma	16616336	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Ependymoma	20639864	CNVD
Schizophrenia	19197363	CNVD

Chromatin state (count:608 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:96628200-96629000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr4:96629000-96629200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr4:96632800-96636400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr4:96635000-96636600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr4:96636400-96637600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr4:96636600-96637400	Enhancers	HMEC	breast
7	chr4:96636800-96637400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr4:96637000-96637600	Enhancers	Placenta Amnion	Placenta Amnion
9	chr4:96637400-96638400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr4:96638400-96638600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr4:96647400-96647600	Enhancers	Breast Myoepithelial Primary Cells	Breast
12	chr4:96647400-96648200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr4:96647600-96650200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
14	chr4:96648200-96648400	Enhancers	ES-I3 Cell Line	embryonic stem cell
15	chr4:96648600-96649200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr4:96648600-96653200	Weak transcription	HMEC	breast
17	chr4:96648800-96649400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr4:96649000-96649600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
19	chr4:96649200-96649400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr4:96649200-96649600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr4:96649400-96649800	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
22	chr4:96649400-96649800	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr4:96649600-96649800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
24	chr4:96649600-96653400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr4:96649800-96650800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr4:96650200-96650600	Enhancers	ES-I3 Cell Line	embryonic stem cell
27	chr4:96650200-96650800	Enhancers	Breast Myoepithelial Primary Cells	Breast
28	chr4:96650200-96651400	Enhancers	HUES6 Cell Line	embryonic stem cell
29	chr4:96650400-96651200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
30	chr4:96650400-96651200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
31	chr4:96650400-96651200	Enhancers	HUES64 Cell Line	embryonic stem cell
32	chr4:96650400-96651600	Enhancers	H1 Cell Line	embryonic stem cell
33	chr4:96650400-96651600	Enhancers	HUES48 Cell Line	embryonic stem cell
34	chr4:96650400-96651600	Enhancers	iPS-15b Cell Line	embryonic stem cell
35	chr4:96650400-96651800	Enhancers	H9 Cell Line	embryonic stem cell
36	chr4:96650400-96651800	Enhancers	iPS-18 Cell Line	embryonic stem cell
37	chr4:96650400-96652000	Enhancers	iPS-20b Cell Line	embryonic stem cell
38	chr4:96650600-96651000	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
39	chr4:96650800-96651200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
40	chr4:96651000-96651400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
41	chr4:96651000-96651600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr4:96651000-96651800	Enhancers	ES-I3 Cell Line	embryonic stem cell
43	chr4:96651200-96652200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr4:96651200-96652400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
45	chr4:96651400-96652400	Weak transcription	HUES6 Cell Line	embryonic stem cell
46	chr4:96651400-96652400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
47	chr4:96651800-96652200	Weak transcription	H9 Cell Line	embryonic stem cell
48	chr4:96651800-96660600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
49	chr4:96652200-96652800	Enhancers	H9 Cell Line	embryonic stem cell
50	chr4:96652400-96652600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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