Variant report

Variant	nsv1013825
Chromosome Location	chr3:298104-354495
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	chr3:319829-320847	GM12878	blood:	n/a	n/a
3	ATF2	chr3:331761-332103	GM12878	blood:	n/a	n/a
4	ATF2	chr3:319964-320748	GM12878	blood:	n/a	n/a
5	ATF3	chr3:306304-306760	A549	lung:	n/a	n/a
6	BATF	chr3:319906-320293	GM12878	blood:	n/a	n/a
7	BATF	chr3:341729-341996	GM12878	blood:	n/a	n/a
8	BATF	chr3:319974-320310	GM12878	blood:	n/a	n/a
9	BATF	chr3:320384-320805	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	chr3:306286-306823	HepG2	liver:	n/a	n/a
17	BHLHE40	chr3:319378-320826	GM12878	blood:	n/a	n/a
18	BHLHE40	chr3:342270-342502	GM12878	blood:	n/a	n/a
19	BRCA1	chr3:306406-306600	HepG2	liver:	n/a	n/a
20	BRCA1	chr3:306367-306903	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr3:306302-306792	HepG2	liver:	n/a	chr3:306309-306322 chr3:306463-306480
22	CEBPB	chr3:306302-306622	MCF-7	breast:	n/a	chr3:306309-306322 chr3:306463-306480
23	CEBPB	chr3:306243-306864	HepG2	liver:	n/a	chr3:306309-306322 chr3:306463-306480
24	CEBPB	chr3:306266-306559	MCF-7	breast:	n/a	chr3:306309-306322 chr3:306463-306480
25	CEBPB	chr3:306097-307016	A549	lung:	n/a	chr3:306309-306322 chr3:306463-306480
26	CEBPB	chr3:306264-306872	IMR90	lung:	n/a	chr3:306309-306322 chr3:306463-306480
27	CEBPB	chr3:306278-306814	A549	lung:	n/a	chr3:306309-306322 chr3:306463-306480
28	CEBPB	chr3:320077-320362	HepG2	liver:	n/a	chr3:320218-320229
29	CEBPB	chr3:306282-306969	HepG2	liver:	n/a	chr3:306309-306322 chr3:306463-306480
30	CEBPB	chr3:302689-302981	Hela-S3	cervix:	n/a	chr3:302812-302825
31	CEBPB	chr3:306177-307012	Hela-S3	cervix:	n/a	chr3:306309-306322 chr3:306463-306480
32	CEBPB	chr3:306264-306781	A549	lung:	n/a	chr3:306309-306322 chr3:306463-306480
33	CEBPB	chr3:306331-306724	HepG2	liver:	n/a	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	chr3:299561-299956	H1-hESC	embryonic stem cell:	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	CREB1	chr3:306373-306822	A549	lung:	n/a	n/a
41	CTCF	chr3:340160-340310	HUVEC	blood vessel:	n/a	n/a
42	CUX1	chr3:341633-342014	GM12878	blood:	n/a	n/a
43	CUX1	chr3:319594-320940	GM12878	blood:	n/a	n/a
44	E2F4	chr3:298337-298540	MCF10A-Er-Src	breast:	n/a	chr3:298525-298534
45	E2F4	chr3:306302-306616	MCF10A-Er-Src	breast:	n/a	n/a
46	E2F6	chr3:299503-299921	H1-hESC	embryonic stem cell:	n/a	n/a
47	EBF1	chr3:319862-320350	GM12878	blood:	n/a	chr3:320133-320146 chr3:320135-320144 chr3:320135-320145 chr3:320134-320145
48	EBF1	chr3:331685-332343	GM12878	blood:	n/a	n/a
49	EBF1	chr3:322153-323052	GM12878	blood:	n/a	chr3:322704-322715
50	EBF1	chr3:319831-320407	GM12878	blood:	n/a	chr3:320133-320146 chr3:320135-320144 chr3:320135-320145 chr3:320134-320145

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:350503-350553	LNCaP	prostate:	n/a
2	chr3:350789-350839	AG10803	skin:	n/a
3	chr3:350892-350942	HepG2	liver:	n/a
4	chr3:350503-350553	LNCaP	prostate:	n/a
5	chr3:350789-350839	AG10803	skin:	n/a
6	chr3:350892-350942	HepG2	liver:	n/a
7	chr3:350892-350942	LNCaP	prostate:	n/a
8	chr3:351003-351053	AG04449	skin:	fetal
9	chr3:350503-350553	AoSMC	blood vessel:	n/a
10	chr3:350602-350652	HCT-116	colon:	n/a
11	chr3:350503-350553	T-47D	breast:	n/a
12	chr3:350789-350839	AG09309	skin:	n/a
13	chr3:351003-351053	HRPEpiC	eye:	n/a
14	chr3:350892-350942	ECC-1	luminal epithelium:	n/a
15	chr3:350789-350839	HEEpiC	esophagus:	n/a
16	chr3:350789-350839	Jurkat	blood:	n/a
17	chr3:350503-350553	ovcar-3	ovarian:	n/a
18	chr3:350682-350732	LNCaP	prostate:	n/a
19	chr3:347869-347919	HRCEpiC	kidney:	n/a
20	chr3:353166-353216	GM12878	blood:	n/a
21	chr3:347869-347919	LNCaP	prostate:	n/a
22	chr3:347869-347919	HIPEpiC	eye:	n/a
23	chr3:347869-347919	GM12878	blood:	n/a
24	chr3:350682-350732	BJ	skin:	n/a
25	chr3:350789-350839	HIPEpiC	eye:	n/a
26	chr3:347869-347919	MCF10A-Er-Src	breast:	n/a
27	chr3:351003-351053	NH-A	brain:	n/a
28	chr3:353166-353216	PrEC	prostate:	n/a
29	chr3:350503-350553	HRCEpiC	kidney:	n/a
30	chr3:350892-350942	SK-N-MC	brain:	n/a
31	chr3:353166-353216	BJ	skin:	n/a
32	chr3:350682-350732	IMR90	lung:	fetal
33	chr3:350602-350652	AG04449	skin:	fetal
34	chr3:347869-347919	SK-N-MC	brain:	n/a
35	chr3:350602-350652	MCF10A-Er-Src	breast:	n/a
36	chr3:350892-350942	Hela-S3	cervix:	n/a
37	chr3:350602-350652	HCPEpiC	choroid plexus:	n/a
38	chr3:353166-353216	HRE	kidney:	n/a
39	chr3:350789-350839	HAEpiC	amniotic membrane:	n/a
40	chr3:350789-350839	GM12891	blood:	n/a
41	chr3:350682-350732	K562	blood:	n/a
42	chr3:350503-350553	PrEC	prostate:	n/a
43	chr3:350602-350652	SK-N-SH	brain:	n/a
44	chr3:350789-350839	HL-60	blood:	n/a
45	chr3:350602-350652	RPTEC	kidney:	n/a
46	chr3:351003-351053	HepG2	liver:	n/a
47	chr3:350602-350652	HNPCEpiC	eye:	n/a
48	chr3:350789-350839	PrEC	prostate:	n/a
49	chr3:350789-350839	BJ	skin:	n/a
50	chr3:353166-353216	PFSK-1	brain:	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	chr3:333238..334968-chr3:337821..339342,2	MCF-7	breast:
4	chr3:321596..323780-chr3:337949..340526,2	MCF-7	breast:
5	chr3:297411..299702-chr3:300779..302869,2	K562	blood:
6	chr3:297411..299702-chr3:300779..302869,2	K562	blood:

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: 2710 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:2710 , 50 per page) page: 1 2 3 4 5 6 7 ... 55

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs432685	chr3:298171-298172	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs182854410	chr3:298180-298181	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs58207874	chr3:298199-298200	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs408644	chr3:298213-298214	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs536612102	chr3:298220-298221	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs75368261	chr3:298244-298245	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs569766280	chr3:298268-298269	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs61476966	chr3:298283-298284	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs561085724	chr3:298305-298306	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs188705346	chr3:298326-298327	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs455187	chr3:298355-298356	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs540896818	chr3:298382-298383	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs553198481	chr3:298395-298396	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs574665565	chr3:298402-298403	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs541800981	chr3:298418-298419	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs563282613	chr3:298419-298420	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs530564413	chr3:298421-298422	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs461010	chr3:298458-298459	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs141545436	chr3:298460-298461	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs144485707	chr3:298461-298462	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs547686702	chr3:298466-298467	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs566332459	chr3:298490-298491	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs192987023	chr3:298500-298501	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs548136223	chr3:298540-298541	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs569703875	chr3:298600-298601	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs537093946	chr3:298604-298605	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs558604344	chr3:298623-298624	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs375678188	chr3:298641-298642	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs570890628	chr3:298793-298794	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs6798880	chr3:298819-298820	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs552894908	chr3:298866-298867	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs369038	chr3:298867-298868	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs185685698	chr3:298887-298888	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs557341112	chr3:298902-298903	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs551632601	chr3:298911-298912	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs575293430	chr3:298932-298933	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs188898438	chr3:298934-298935	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs564170706	chr3:298946-298947	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs528192804	chr3:298956-298957	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs192667471	chr3:298960-298961	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs147853993	chr3:298968-298969	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs11714385	chr3:298999-299000	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs455239	chr3:299025-299026	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs35247275	chr3:299036-299037	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs71619442	chr3:299052-299053	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs183669464	chr3:299063-299064	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs530798921	chr3:299075-299076	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs552175892	chr3:299079-299080	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs570878720	chr3:299117-299118	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs534819017	chr3:299123-299124	Weak transcription Enhancers	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:233 , 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	chr3:291200-298200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr3:291400-299600	Weak transcription	HUES48 Cell Line	embryonic stem cell
5	chr3:291800-305200	Weak transcription	Brain Germinal Matrix	brain
6	chr3:297000-299600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
7	chr3:297200-299600	Weak transcription	HUES6 Cell Line	embryonic stem cell
8	chr3:297200-299600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr3:297600-299800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
10	chr3:297600-302600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
11	chr3:298000-301000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr3:298200-298400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
13	chr3:299600-299800	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr3:299600-300000	Enhancers	HUES6 Cell Line	embryonic stem cell
15	chr3:299600-300000	Enhancers	Hela-S3	cervix
16	chr3:299600-300200	Enhancers	HUES48 Cell Line	embryonic stem cell
17	chr3:299600-300200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr3:299600-300400	Enhancers	iPS-18 Cell Line	embryonic stem cell
19	chr3:299600-301000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
20	chr3:299800-300000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr3:299800-300000	Enhancers	Breast Myoepithelial Primary Cells	Breast
22	chr3:299800-300200	Enhancers	ES-I3 Cell Line	embryonic stem cell
23	chr3:300000-300200	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr3:300000-305200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
25	chr3:300200-301000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr3:300200-304600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
27	chr3:300800-301000	Enhancers	Fetal Brain Male	brain
28	chr3:301000-302000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr3:301000-302200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
30	chr3:301000-304800	Weak transcription	Fetal Brain Male	brain
31	chr3:302000-303400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr3:302200-303200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr3:302400-306200	Weak transcription	Pancreatic Islets	Pancreatic Islet
34	chr3:302600-303200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr3:303200-305600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr3:303200-306000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
37	chr3:303400-304400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr3:304400-307600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr3:304600-304800	Enhancers	Fetal Brain Female	brain
40	chr3:304600-307000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr3:304800-305800	Enhancers	Fetal Brain Male	brain
42	chr3:305000-307800	Enhancers	HepG2	liver
43	chr3:305200-305800	Enhancers	Brain Germinal Matrix	brain
44	chr3:305400-307800	Enhancers	Hela-S3	cervix
45	chr3:305600-305800	Enhancers	HMEC	breast
46	chr3:305600-306000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
47	chr3:305600-307000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr3:305800-306200	Enhancers	A549	lung
49	chr3:305800-306400	Weak transcription	HMEC	breast
50	chr3:305800-306800	Enhancers	Muscle Satellite Cultured Cells	--

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