Variant report

Variant	nsv1000884
Chromosome Location	chr3:300020-354398
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	ARID3A	chr3:305517-307368	HepG2	liver:	n/a	n/a
2	ATF2	chr3:331761-332103	GM12878	blood:	n/a	n/a
3	ATF2	chr3:319964-320748	GM12878	blood:	n/a	n/a
4	ATF2	chr3:319829-320847	GM12878	blood:	n/a	n/a
5	ATF3	chr3:306304-306760	A549	lung:	n/a	n/a
6	BATF	chr3:341729-341996	GM12878	blood:	n/a	n/a
7	BATF	chr3:320384-320805	GM12878	blood:	n/a	n/a
8	BATF	chr3:319974-320310	GM12878	blood:	n/a	n/a
9	BATF	chr3:319906-320293	GM12878	blood:	n/a	n/a
10	BCL11A	chr3:319942-320280	GM12878	blood:	n/a	chr3:320201-320210 chr3:320061-320069
11	BCL11A	chr3:319927-320341	GM12878	blood:	n/a	chr3:320201-320210 chr3:320061-320069
12	BCL3	chr3:320464-320727	GM12878	blood:	n/a	n/a
13	BCL3	chr3:306315-306750	A549	lung:	n/a	n/a
14	BCL3	chr3:306168-306863	A549	lung:	n/a	chr3:306285-306294 chr3:306282-306291
15	BCLAF1	chr3:320388-320763	GM12878	blood:	n/a	n/a
16	BHLHE40	chr3:342270-342502	GM12878	blood:	n/a	n/a
17	BHLHE40	chr3:319378-320826	GM12878	blood:	n/a	n/a
18	BHLHE40	chr3:306286-306823	HepG2	liver:	n/a	n/a
19	BRCA1	chr3:306367-306903	Hela-S3	cervix:	n/a	n/a
20	BRCA1	chr3:306406-306600	HepG2	liver:	n/a	n/a
21	CEBPB	chr3:306177-307012	Hela-S3	cervix:	n/a	chr3:306309-306322 chr3:306463-306480
22	CEBPB	chr3:306243-306864	HepG2	liver:	n/a	chr3:306309-306322 chr3:306463-306480
23	CEBPB	chr3:306331-306724	HepG2	liver:	n/a	chr3:306463-306480
24	CEBPB	chr3:306264-306872	IMR90	lung:	n/a	chr3:306309-306322 chr3:306463-306480
25	CEBPB	chr3:302689-302981	Hela-S3	cervix:	n/a	chr3:302812-302825
26	CEBPB	chr3:306278-306814	A549	lung:	n/a	chr3:306309-306322 chr3:306463-306480
27	CEBPB	chr3:306266-306559	MCF-7	breast:	n/a	chr3:306309-306322 chr3:306463-306480
28	CEBPB	chr3:306302-306622	MCF-7	breast:	n/a	chr3:306309-306322 chr3:306463-306480
29	CEBPB	chr3:306282-306969	HepG2	liver:	n/a	chr3:306309-306322 chr3:306463-306480
30	CEBPB	chr3:306264-306781	A549	lung:	n/a	chr3:306309-306322 chr3:306463-306480
31	CEBPB	chr3:320077-320362	HepG2	liver:	n/a	chr3:320218-320229
32	CEBPB	chr3:306302-306792	HepG2	liver:	n/a	chr3:306309-306322 chr3:306463-306480
33	CEBPB	chr3:306097-307016	A549	lung:	n/a	chr3:306309-306322 chr3:306463-306480
34	CEBPD	chr3:306328-306607	HepG2	liver:	n/a	n/a
35	CHD1	chr3:341448-341614	GM12878	blood:	n/a	n/a
36	CHD2	chr3:319756-320739	GM12878	blood:	n/a	n/a
37	CREB1	chr3:306373-306822	A549	lung:	n/a	n/a
38	CREB1	chr3:306269-306913	HepG2	liver:	n/a	n/a
39	CREB1	chr3:306196-306931	HepG2	liver:	n/a	n/a
40	CTCF	chr3:340160-340310	HUVEC	blood vessel:	n/a	n/a
41	CUX1	chr3:319594-320940	GM12878	blood:	n/a	n/a
42	CUX1	chr3:341633-342014	GM12878	blood:	n/a	n/a
43	E2F4	chr3:306302-306616	MCF10A-Er-Src	breast:	n/a	n/a
44	EBF1	chr3:319862-320350	GM12878	blood:	n/a	chr3:320133-320146 chr3:320135-320144 chr3:320135-320145 chr3:320134-320145
45	EBF1	chr3:322542-322796	GM12878	blood:	n/a	chr3:322704-322715
46	EBF1	chr3:319068-320868	GM12878	blood:	n/a	chr3:320133-320146 chr3:320135-320144 chr3:320135-320145 chr3:320134-320145
47	EBF1	chr3:341471-342010	GM12878	blood:	n/a	n/a
48	EBF1	chr3:312560-312707	GM12878	blood:	n/a	n/a
49	EBF1	chr3:331685-332343	GM12878	blood:	n/a	n/a
50	EBF1	chr3:322153-323052	GM12878	blood:	n/a	chr3:322704-322715

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:350789-350839	NHDF-neo	bronchial:	n/a
2	chr3:350789-350839	NHDF-neo	bronchial:	n/a
3	chr3:353166-353216	Hepatocyte	liver:	n/a
4	chr3:350503-350553	Hepatocyte	liver:	n/a
5	chr3:350892-350942	GM19239	blood:	n/a
6	chr3:350892-350942	SK-N-SH_RA	brain:	n/a
7	chr3:350503-350553	HEEpiC	esophagus:	n/a
8	chr3:350503-350553	IMR90	lung:	fetal
9	chr3:350503-350553	Hela-S3	cervix:	n/a
10	chr3:350892-350942	Hela-S3	cervix:	n/a
11	chr3:351003-351053	HPAEpiC	pulmonary alveolar:	n/a
12	chr3:350892-350942	T-47D	breast:	n/a
13	chr3:351003-351053	A549	lung:	n/a
14	chr3:353166-353216	A549	lung:	n/a
15	chr3:350682-350732	NT2-D1	testis:	n/a
16	chr3:350682-350732	HRE	kidney:	n/a
17	chr3:350602-350652	IMR90	lung:	fetal
18	chr3:350503-350553	NHDF-neo	bronchial:	n/a
19	chr3:350789-350839	H1-hESC	embryonic stem cell:	embryo
20	chr3:350503-350553	CMK	blood:	n/a
21	chr3:350892-350942	AG10803	skin:	n/a
22	chr3:347869-347919	AG10803	skin:	n/a
23	chr3:350789-350839	GM12891	blood:	n/a
24	chr3:350789-350839	MCF10A-Er-Src	breast:	n/a
25	chr3:350503-350553	SKMC	muscle:	n/a
26	chr3:350892-350942	K562	blood:	n/a
27	chr3:350503-350553	K562	blood:	n/a
28	chr3:350789-350839	PrEC	prostate:	n/a
29	chr3:350682-350732	Caco-2	colon:	n/a
30	chr3:350503-350553	GM12892	blood:	n/a
31	chr3:351003-351053	GM19239	blood:	n/a
32	chr3:350789-350839	HPAEpiC	pulmonary alveolar:	n/a
33	chr3:351003-351053	CMK	blood:	n/a
34	chr3:350503-350553	BJ	skin:	n/a
35	chr3:350682-350732	ovcar-3	ovarian:	n/a
36	chr3:350789-350839	HRPEpiC	eye:	n/a
37	chr3:353166-353216	HAEpiC	amniotic membrane:	n/a
38	chr3:347869-347919	NHDF-neo	bronchial:	n/a
39	chr3:350682-350732	HCPEpiC	choroid plexus:	n/a
40	chr3:350602-350652	HUVEC	blood vessel:	n/a
41	chr3:350503-350553	NT2-D1	testis:	n/a
42	chr3:350892-350942	ovcar-3	ovarian:	n/a
43	chr3:347869-347919	Caco-2	colon:	n/a
44	chr3:350892-350942	SK-N-SH	brain:	n/a
45	chr3:353166-353216	AG10803	skin:	n/a
46	chr3:353166-353216	SK-N-SH_RA	brain:	n/a
47	chr3:351003-351053	HAEpiC	amniotic membrane:	n/a
48	chr3:350602-350652	K562	blood:	n/a
49	chr3:351003-351053	K562	blood:	n/a
50	chr3:347869-347919	Hela-S3	cervix:	n/a

No.	Distal block	Cell Line	Cell type
1	chr3:333238..334968-chr3:337821..339342,2	MCF-7	breast:
2	chr3:321596..323780-chr3:337949..340526,2	MCF-7	breast:
3	chr3:321596..323780-chr3:337949..340526,2	MCF-7	breast:
4	chr3:297411..299702-chr3:300779..302869,2	K562	blood:
5	chr3:333238..334968-chr3:337821..339342,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-IL5RA-15	chr3:350397-351005	NONHSAT087564

Variant related genes	Relation type
RNU6-1194P	TF binding region
RPS8P6	TF binding region
RNU6-1194P	CpG island
RPS8P6	CpG island

Extended variants
information (count: 2603 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:2603 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs184128451	chr3:300021-300022	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs138356477	chr3:300105-300106	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs572923736	chr3:300145-300146	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs533198015	chr3:300175-300176	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs190222512	chr3:300202-300203	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs141554910	chr3:300207-300208	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs533521038	chr3:300220-300221	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs543836733	chr3:300226-300227	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs181840759	chr3:300255-300256	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs566982249	chr3:300261-300262	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs35024995	chr3:300304-300305	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs187298477	chr3:300306-300307	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs111627099	chr3:300310-300311	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs577382254	chr3:300313-300314	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs558136523	chr3:300322-300323	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs573505550	chr3:300328-300329	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs192006453	chr3:300331-300332	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs73092546	chr3:300341-300342	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs138492395	chr3:300342-300343	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs369992092	chr3:300375-300376	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs529344434	chr3:300379-300380	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs73092548	chr3:300383-300384	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs73092549	chr3:300396-300397	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs180750132	chr3:300443-300444	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs78660655	chr3:300447-300448	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs73092552	chr3:300451-300452	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs539798755	chr3:300547-300548	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs568371646	chr3:300549-300550	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs527593132	chr3:300550-300551	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs548907441	chr3:300551-300552	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs372557017	chr3:300552-300553	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs369192728	chr3:300577-300578	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs538887029	chr3:300617-300618	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs558180731	chr3:300618-300619	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs77510233	chr3:300632-300633	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs376677282	chr3:300634-300635	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs79824751	chr3:300635-300636	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs150310699	chr3:300641-300642	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs10687230	chr3:300642-300643	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs555826075	chr3:300701-300702	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs190074883	chr3:300705-300706	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs148772885	chr3:300707-300708	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs558336146	chr3:300753-300754	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs368943872	chr3:300782-300783	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs540908946	chr3:300814-300815	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs556140962	chr3:300832-300833	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs182656547	chr3:300833-300834	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs544650706	chr3:300834-300835	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs6808502	chr3:300884-300885	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs79202223	chr3:300912-300913	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:84)

Disease	PMID	Source
Cancer	20164920	CNVD
Lung cancer	16618734	CNVD
Autism	18349135	CNVD
Breast cancer	20409316	CNVD
Myelofibrosis	22110671	CNVD
Autism	22241247	CNVD
Intellectual disability	22045946	CNVD
Squamous cell cancer	19607727	CNVD
Gastric adenocarcinoma	19115996	CNVD
sporadic birth defects	19047251	CNVD
Mental retardation	17124404	CNVD
abnormal development	18461090	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Sudden cardiac death	19188705	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ovarian cancer	21720365	CNVD
Neuroblastoma	18923191	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Biliary cancer	19435499	CNVD
Medulloblastoma	21979893	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Breast cancer	17603634	CNVD
Neuroblastoma	17327916	CNVD
Glioblastoma multiforme	21080181	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
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
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Schizophrenia	20967226	CNVD
Autism	22543975	CNVD
Attention deficit hyperactivity disorder	19546859	CNVD
lymphocytic leukemia	21291569	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	21668985	CNVD
Tetralogy of Fallot	22912587	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Autism	20685689	CNVD
Melanoma	20877625	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Hodgkin''s lymphoma	17606441	CNVD

Chromatin state (count:220 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:285400-307400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
2	chr3:286200-315400	Weak transcription	Ovary	ovary
3	chr3:291800-305200	Weak transcription	Brain Germinal Matrix	brain
4	chr3:297600-302600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr3:298000-301000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr3:299600-300200	Enhancers	HUES48 Cell Line	embryonic stem cell
7	chr3:299600-300200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr3:299600-300400	Enhancers	iPS-18 Cell Line	embryonic stem cell
9	chr3:299600-301000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
10	chr3:299800-300200	Enhancers	ES-I3 Cell Line	embryonic stem cell
11	chr3:300000-300200	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr3:300000-305200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
13	chr3:300200-301000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr3:300200-304600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr3:300800-301000	Enhancers	Fetal Brain Male	brain
16	chr3:301000-302000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr3:301000-302200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr3:301000-304800	Weak transcription	Fetal Brain Male	brain
19	chr3:302000-303400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr3:302200-303200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr3:302400-306200	Weak transcription	Pancreatic Islets	Pancreatic Islet
22	chr3:302600-303200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr3:303200-305600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr3:303200-306000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chr3:303400-304400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr3:304400-307600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr3:304600-304800	Enhancers	Fetal Brain Female	brain
28	chr3:304600-307000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr3:304800-305800	Enhancers	Fetal Brain Male	brain
30	chr3:305000-307800	Enhancers	HepG2	liver
31	chr3:305200-305800	Enhancers	Brain Germinal Matrix	brain
32	chr3:305400-307800	Enhancers	Hela-S3	cervix
33	chr3:305600-305800	Enhancers	HMEC	breast
34	chr3:305600-306000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
35	chr3:305600-307000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr3:305800-306200	Enhancers	A549	lung
37	chr3:305800-306400	Weak transcription	HMEC	breast
38	chr3:305800-306800	Enhancers	Muscle Satellite Cultured Cells	--
39	chr3:305800-308400	Weak transcription	Fetal Brain Male	brain
40	chr3:305800-308600	Weak transcription	Brain Germinal Matrix	brain
41	chr3:306000-307400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
42	chr3:306200-306400	Enhancers	Pancreatic Islets	Pancreatic Islet
43	chr3:306200-306800	Flanking Active TSS	A549	lung
44	chr3:306400-306600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
45	chr3:306400-306800	Enhancers	Brain Substantia Nigra	brain
46	chr3:306400-307000	Enhancers	HMEC	breast
47	chr3:306600-306800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
48	chr3:306600-307000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
49	chr3:306600-307000	Enhancers	NH-A	brain
50	chr3:306800-308400	Enhancers	A549	lung

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