Variant report

Variant	nsv1000596
Chromosome Location	chr3:20428568-20501468
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:132)
CpG islands
(count:61)
Chromatin interactive
region (count:7)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:132 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr3:20492146-20492486	K562	blood:	n/a	n/a
2	BACH1	chr3:20492139-20492474	H1-hESC	embryonic stem cell:	n/a	n/a
3	CCNT2	chr3:20500973-20501023	K562	blood:	n/a	n/a
4	CEBPB	chr3:20439770-20440049	A549	lung:	n/a	n/a
5	CEBPB	chr3:20439832-20440032	H1-hESC	embryonic stem cell:	n/a	n/a
6	CEBPB	chr3:20439795-20440063	K562	blood:	n/a	n/a
7	CEBPB	chr3:20442866-20443121	HepG2	liver:	n/a	chr3:20442974-20442985
8	CEBPB	chr3:20447358-20447747	HepG2	liver:	n/a	chr3:20447481-20447492
9	CEBPB	chr3:20439757-20440083	IMR90	lung:	n/a	n/a
10	CEBPB	chr3:20439732-20440080	HepG2	liver:	n/a	n/a
11	CTCF	chr3:20473944-20474006	GM20000	blood:	n/a	n/a
12	CTCF	chr3:20476860-20477010	GM12869	blood:	n/a	n/a
13	CTCF	chr3:20485260-20485324	GM10266	blood:	n/a	n/a
14	CTCF	chr3:20468507-20468543	Lung_OC	lung:	n/a	n/a
15	CTCF	chr3:20440798-20440832	Pancreas_OC	pancreas:	n/a	n/a
16	CTCF	chr3:20448200-20448350	GM12871	blood:	n/a	n/a
17	E2F4	chr3:20447363-20447582	MCF10A-Er-Src	breast:	n/a	n/a
18	E2F4	chr3:20478080-20478220	MCF10A-Er-Src	breast:	n/a	n/a
19	E2F4	chr3:20496696-20496745	MCF10A-Er-Src	breast:	n/a	n/a
20	EP300	chr3:20464757-20464762	K562	blood:	n/a	n/a
21	EP300	chr3:20500889-20501208	SK-N-SH_RA	brain:	n/a	n/a
22	EP300	chr3:20500940-20501145	K562	blood:	n/a	n/a
23	EP300	chr3:20463825-20464440	T-47D	breast:	n/a	n/a
24	EP300	chr3:20463827-20464309	T-47D	breast:	n/a	n/a
25	EP300	chr3:20500898-20501156	SK-N-SH_RA	brain:	n/a	n/a
26	FOS	chr3:20488402-20488562	MCF10A-Er-Src	breast:	n/a	n/a
27	FOS	chr3:20447261-20447639	MCF10A-Er-Src	breast:	n/a	n/a
28	FOS	chr3:20447997-20448170	MCF10A-Er-Src	breast:	n/a	n/a
29	FOS	chr3:20461130-20461235	MCF10A-Er-Src	breast:	n/a	chr3:20461183-20461194 chr3:20461185-20461197 chr3:20461187-20461195
30	FOS	chr3:20461137-20461236	MCF10A-Er-Src	breast:	n/a	chr3:20461183-20461194 chr3:20461185-20461197 chr3:20461187-20461195
31	FOS	chr3:20442889-20443042	MCF10A-Er-Src	breast:	n/a	chr3:20443032-20443041
32	FOS	chr3:20447238-20447631	MCF10A-Er-Src	breast:	n/a	n/a
33	FOS	chr3:20477810-20478010	MCF10A-Er-Src	breast:	n/a	n/a
34	FOS	chr3:20477790-20477990	MCF10A-Er-Src	breast:	n/a	n/a
35	FOS	chr3:20447258-20447674	MCF10A-Er-Src	breast:	n/a	n/a
36	FOS	chr3:20461170-20461267	MCF10A-Er-Src	breast:	n/a	chr3:20461183-20461194 chr3:20461185-20461197 chr3:20461187-20461195
37	FOS	chr3:20447289-20447627	MCF10A-Er-Src	breast:	n/a	n/a
38	FOXA1	chr3:20463848-20464374	T-47D	breast:	n/a	n/a
39	FOXA1	chr3:20463817-20464382	T-47D	breast:	n/a	n/a
40	FOXA1	chr3:20435940-20436185	ECC-1	luminal epithelium:	n/a	n/a
41	FOXA2	chr3:20474218-20474575	A549	lung:	n/a	n/a
42	GATA2	chr3:20500915-20501173	K562	blood:	n/a	chr3:20500991-20501012 chr3:20501103-20501116
43	GATA2	chr3:20500910-20501219	SH-SY5Y	brain:	n/a	chr3:20500991-20501012 chr3:20501103-20501116
44	GATA3	chr3:20445867-20445937	SH-SY5Y	brain:	n/a	n/a
45	GATA3	chr3:20449226-20449426	SH-SY5Y	brain:	n/a	chr3:20449296-20449303 chr3:20449292-20449305 chr3:20449373-20449384 chr3:20449273-20449290
46	GATA3	chr3:20439775-20439904	SH-SY5Y	brain:	n/a	n/a
47	GATA3	chr3:20500708-20501140	SH-SY5Y	brain:	n/a	chr3:20500991-20501012 chr3:20501103-20501116
48	GATA3	chr3:20454811-20455074	T-47D	breast:	n/a	n/a
49	GATA3	chr3:20481760-20481905	SH-SY5Y	brain:	n/a	n/a
50	GATA3	chr3:20463888-20464339	T-47D	breast:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:20448283-20448333	GM12878	blood:	n/a
2	chr3:20448283-20448333	H1-hESC	embryonic stem cell:	embryo
3	chr3:20448283-20448333	K562	blood:	n/a
4	chr3:20448283-20448333	AG09309	skin:	n/a
5	chr3:20448283-20448333	HL-60	blood:	n/a
6	chr3:20448283-20448333	HCM	heart:	n/a
7	chr3:20448283-20448333	SAEC	small airway:	n/a
8	chr3:20448283-20448333	GM06990	blood:	n/a
9	chr3:20448283-20448333	NB4	blood:	n/a
10	chr3:20448283-20448333	HPAEpiC	pulmonary alveolar:	n/a
11	chr3:20448283-20448333	PANC-1	pancreas:	n/a
12	chr3:20448283-20448333	BE2_C	brain:	n/a
13	chr3:20448283-20448333	HIPEpiC	eye:	n/a
14	chr3:20448283-20448333	SK-N-MC	brain:	n/a
15	chr3:20448283-20448333	AG10803	skin:	n/a
16	chr3:20448283-20448333	AG09319	gingival:	n/a
17	chr3:20448283-20448333	A549	lung:	n/a
18	chr3:20448283-20448333	NT2-D1	testis:	n/a
19	chr3:20448283-20448333	HNPCEpiC	eye:	n/a
20	chr3:20448283-20448333	MCF-7	breast:	n/a
21	chr3:20448283-20448333	SK-N-SH	brain:	n/a
22	chr3:20448283-20448333	NHDF-neo	bronchial:	n/a
23	chr3:20448283-20448333	PrEC	prostate:	n/a
24	chr3:20448283-20448333	HEK293	kidney:	embryo
25	chr3:20448283-20448333	T-47D	breast:	n/a
26	chr3:20448283-20448333	GM12891	blood:	n/a
27	chr3:20448283-20448333	HMEC	breast:	n/a
28	chr3:20448283-20448333	ProgFib	skin:	n/a
29	chr3:20448283-20448333	BJ	skin:	n/a
30	chr3:20448283-20448333	HRE	kidney:	n/a
31	chr3:20448283-20448333	HCPEpiC	choroid plexus:	n/a
32	chr3:20448283-20448333	NHBE	bronchial:	n/a
33	chr3:20448283-20448333	Hela-S3	cervix:	n/a
34	chr3:20448283-20448333	AG04450	lung:	fetal
35	chr3:20448283-20448333	AG04449	skin:	fetal
36	chr3:20448283-20448333	AoSMC	blood vessel:	n/a
37	chr3:20448283-20448333	MCF10A-Er-Src	breast:	n/a
38	chr3:20448283-20448333	ECC-1	luminal epithelium:	n/a
39	chr3:20448283-20448333	HRPEpiC	eye:	n/a
40	chr3:20448283-20448333	SK-N-SH_RA	brain:	n/a
41	chr3:20448283-20448333	HUVEC	blood vessel:	n/a
42	chr3:20448283-20448333	RPTEC	kidney:	n/a
43	chr3:20448283-20448333	Hepatocyte	liver:	n/a
44	chr3:20448283-20448333	HEEpiC	esophagus:	n/a
45	chr3:20448283-20448333	GM19239	blood:	n/a
46	chr3:20448283-20448333	HCF	heart:	n/a
47	chr3:20448283-20448333	HRCEpiC	kidney:	n/a
48	chr3:20448283-20448333	GM12892	blood:	n/a
49	chr3:20448283-20448333	HAEpiC	amniotic membrane:	n/a
50	chr3:20448283-20448333	LNCaP	prostate:	n/a

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:20436330..20438604-chr3:20439437..20442062,2	MCF-7	breast:
2	chr3:20460438..20462411-chr3:20516734..20518648,2	MCF-7	breast:
3	chr3:20447764..20450202-chr3:20450641..20452829,2	MCF-7	breast:
4	chr3:20436330..20438604-chr3:20439437..20442062,2	MCF-7	breast:
5	chr3:20451777..20453884-chr3:20476566..20478123,2	K562	blood:
6	chr3:20451777..20453884-chr3:20476566..20478123,2	K562	blood:
7	chr3:20447764..20450202-chr3:20450641..20452829,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KAT2B-3	chr3:20429741-20432054	ENSG00000261734.1

No data

Variant related genes	Relation type
ENSG00000261734	TF binding region
ENSG00000261734	CpG island

Extended variants
information (count: 1578 )
Associated
traits (count: 76 )

Variant overlapped rSNPs/rCNVs (count:1578 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs13098833	chr3:20428568-20428569	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs565343029	chr3:20428604-20428605	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs539895382	chr3:20428688-20428689	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs114024896	chr3:20428704-20428705	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs13099614	chr3:20428736-20428737	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs373895121	chr3:20428787-20428788	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs117169140	chr3:20428792-20428793	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs13079172	chr3:20428793-20428794	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs368337224	chr3:20428828-20428829	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs548736906	chr3:20428833-20428834	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs6768831	chr3:20428841-20428842	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs562224616	chr3:20428947-20428948	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs193256595	chr3:20428968-20428969	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs571475056	chr3:20428972-20428973	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs538811083	chr3:20428984-20428985	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs9882627	chr3:20428998-20428999	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs566215872	chr3:20429015-20429016	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs59468557	chr3:20429066-20429067	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs368309781	chr3:20429098-20429099	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs576339135	chr3:20429116-20429117	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs559633971	chr3:20429138-20429139	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs543769909	chr3:20429156-20429157	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs141213187	chr3:20429157-20429158	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs577043974	chr3:20429194-20429195	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs150738389	chr3:20429215-20429216	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs115109677	chr3:20429216-20429217	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs139056038	chr3:20429244-20429245	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs532077402	chr3:20429290-20429291	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs542701325	chr3:20429325-20429326	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs560723616	chr3:20429356-20429357	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs143404383	chr3:20429362-20429363	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs565086079	chr3:20429363-20429364	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs530956091	chr3:20429395-20429396	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs571595530	chr3:20429428-20429429	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs532434605	chr3:20429440-20429441	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs547656445	chr3:20429483-20429484	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs565879187	chr3:20429507-20429508	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs551850036	chr3:20429516-20429517	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs536351310	chr3:20429549-20429550	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs140188062	chr3:20429569-20429570	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs569967768	chr3:20429585-20429586	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs9849499	chr3:20429594-20429595	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs183631507	chr3:20429595-20429596	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs577151158	chr3:20429622-20429623	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs541316920	chr3:20429672-20429673	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs188438963	chr3:20429678-20429679	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs528059478	chr3:20429680-20429681	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs371776618	chr3:20429696-20429697	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs147723207	chr3:20429756-20429757	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
50	rs542365916	chr3:20429758-20429759	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a

Variant related diseases (count:76)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Neuroblastoma	17327916	CNVD
Glioblastoma multiforme	21080181	CNVD
Neuroblastoma	18923191	CNVD
Colorectal cancer	21297112	CNVD
Lynch syndrome	18415027	CNVD
Renal cell carcinoma	18592004	CNVD
Acute myeloid leukemia	20729466	CNVD
Urothelial carcinoma	18382360	CNVD
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Hirschsprung''s Disease	21712996	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Insulin resistance	16721378	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Oral cancer	19627613	CNVD
Renal cell carcinoma	19461508	CNVD
Epithelial cancer	22065749	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Acute myeloid leukemia	16864856	CNVD
Liposarcoma	21253554	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Pancreatic endocrine tumor	20981439	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Oral cancer	21386901	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
lymphocytic leukemia	21291569	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Intellectual disability	22102821	CNVD
Esophageal cancer	20955586	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Myelofibrosis	22110671	CNVD
Gastric adenocarcinoma	19115996	CNVD
Squamous cell cancer	20885788	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Breast cancer	17133270	CNVD
Developmental delay	21147756	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:92 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:20427600-20433200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr3:20433000-20433400	Enhancers	H1 Cell Line	embryonic stem cell
3	chr3:20433000-20433600	Enhancers	iPS-20b Cell Line	embryonic stem cell
4	chr3:20433200-20433400	Enhancers	ES-I3 Cell Line	embryonic stem cell
5	chr3:20433200-20433600	Enhancers	HUES6 Cell Line	embryonic stem cell
6	chr3:20433400-20435800	Weak transcription	H1 Cell Line	embryonic stem cell
7	chr3:20433600-20435800	Weak transcription	HUES6 Cell Line	embryonic stem cell
8	chr3:20435600-20436200	ZNF genes & repeats	Fetal Intestine Small	intestine
9	chr3:20435800-20436000	Enhancers	HUES6 Cell Line	embryonic stem cell
10	chr3:20435800-20436200	Enhancers	H1 Cell Line	embryonic stem cell
11	chr3:20435800-20436200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr3:20435800-20436200	Bivalent Enhancer	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr3:20435800-20436200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr3:20436000-20436200	ZNF genes & repeats	Pancreas	Pancrea
15	chr3:20436000-20448200	Weak transcription	HUES6 Cell Line	embryonic stem cell
16	chr3:20436200-20445200	Weak transcription	Fetal Intestine Small	intestine
17	chr3:20436200-20445800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr3:20436200-20453400	Weak transcription	Pancreas	Pancrea
19	chr3:20437800-20438400	Enhancers	iPS-15b Cell Line	embryonic stem cell
20	chr3:20441400-20442000	Enhancers	Aorta	Aorta
21	chr3:20442200-20443200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
22	chr3:20442800-20443400	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr3:20443200-20443400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
24	chr3:20443200-20446800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr3:20445200-20446200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
26	chr3:20445200-20446200	Enhancers	Small Intestine	intestine
27	chr3:20445200-20447200	Enhancers	Duodenum Mucosa	Duodenum
28	chr3:20445200-20449000	Enhancers	Fetal Intestine Large	intestine
29	chr3:20445200-20450000	Enhancers	Fetal Intestine Small	intestine
30	chr3:20445200-20450000	Enhancers	Fetal Stomach	stomach
31	chr3:20445400-20445600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
32	chr3:20445600-20445800	Enhancers	iPS-15b Cell Line	embryonic stem cell
33	chr3:20445600-20448800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
34	chr3:20445800-20446000	Enhancers	H1 Cell Line	embryonic stem cell
35	chr3:20445800-20446000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
36	chr3:20445800-20448400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
37	chr3:20446000-20446800	Enhancers	Fetal Brain Male	brain
38	chr3:20446000-20447400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr3:20446200-20448200	Weak transcription	H1 Cell Line	embryonic stem cell
40	chr3:20446800-20448200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr3:20447000-20447400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
42	chr3:20447000-20448400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr3:20447000-20448400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
44	chr3:20447200-20447600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr3:20447200-20447800	Enhancers	Muscle Satellite Cultured Cells	--
46	chr3:20447200-20448400	Enhancers	NH-A	brain
47	chr3:20447200-20448400	Enhancers	NHDF-Ad	bronchial
48	chr3:20447400-20447800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
49	chr3:20447400-20448400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr3:20447800-20448400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

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