Variant report

Variant	esv2763279
Chromosome Location	chr3:75958155-76107685
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	chr3:75991836-75991901	K562	blood:	n/a	n/a
2	ATF1	chr3:75986623-75986792	K562	blood:	n/a	n/a
3	ATF1	chr3:75998476-75998676	K562	blood:	n/a	n/a
4	ATF1	chr3:75991766-75991934	K562	blood:	n/a	n/a
5	ATF1	chr3:75986254-75986287	K562	blood:	n/a	n/a
6	ATF1	chr3:75985241-75985450	K562	blood:	n/a	n/a
7	ATF2	chr3:76092805-76093300	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr3:76092810-76093431	H1-hESC	embryonic stem cell:	n/a	n/a
9	BATF	chr3:76091734-76092099	GM12878	blood:	n/a	n/a
10	BATF	chr3:76091730-76092060	GM12878	blood:	n/a	n/a
11	BCL11A	chr3:76091772-76091983	GM12878	blood:	n/a	n/a
12	BCL11A	chr3:76091692-76092106	GM12878	blood:	n/a	n/a
13	BHLHE40	chr3:75991823-75991949	GM12878	blood:	n/a	n/a
14	BHLHE40	chr3:76094241-76094379	GM12878	blood:	n/a	n/a
15	BHLHE40	chr3:75996667-75996686	GM12878	blood:	n/a	n/a
16	BRCA1	chr3:76092875-76093639	H1-hESC	embryonic stem cell:	n/a	n/a
17	CEBPB	chr3:76092893-76093312	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr3:76023773-76024060	A549	lung:	n/a	chr3:76023907-76023918 chr3:76023905-76023918 chr3:76023905-76023918 chr3:76023907-76023916 chr3:76023907-76023916 chr3:76023905-76023916 chr3:76023907-76023916 chr3:76023907-76023916 chr3:76023905-76023918
19	CEBPB	chr3:75991825-75991831	K562	blood:	n/a	n/a
20	CEBPB	chr3:76025393-76025671	HepG2	liver:	n/a	chr3:76025511-76025522
21	CEBPB	chr3:76034619-76034978	A549	lung:	n/a	chr3:76034793-76034804
22	CEBPB	chr3:76034636-76034981	K562	blood:	n/a	chr3:76034793-76034804
23	CEBPB	chr3:76034701-76034915	H1-hESC	embryonic stem cell:	n/a	chr3:76034793-76034804
24	CEBPB	chr3:76093689-76094128	IMR90	lung:	n/a	n/a
25	CEBPB	chr3:76023734-76024093	IMR90	lung:	n/a	chr3:76023907-76023918 chr3:76023905-76023918 chr3:76023905-76023918 chr3:76023907-76023916 chr3:76023907-76023916 chr3:76023905-76023916 chr3:76023907-76023916 chr3:76023907-76023916 chr3:76023905-76023918
26	CEBPB	chr3:76034632-76034971	IMR90	lung:	n/a	chr3:76034793-76034804
27	CEBPB	chr3:76023733-76024088	HepG2	liver:	n/a	chr3:76023907-76023918 chr3:76023905-76023918 chr3:76023905-76023918 chr3:76023907-76023916 chr3:76023907-76023916 chr3:76023905-76023916 chr3:76023907-76023916 chr3:76023907-76023916 chr3:76023905-76023918
28	CEBPB	chr3:76034609-76034974	HepG2	liver:	n/a	chr3:76034793-76034804
29	CEBPB	chr3:76093872-76094087	HepG2	liver:	n/a	n/a
30	CEBPB	chr3:76023890-76023921	H1-hESC	embryonic stem cell:	n/a	chr3:76023907-76023918 chr3:76023905-76023918 chr3:76023905-76023918 chr3:76023907-76023916 chr3:76023907-76023916 chr3:76023905-76023916 chr3:76023907-76023916 chr3:76023907-76023916 chr3:76023905-76023918
31	CEBPZ	chr3:75991161-75991361	HepG2	liver:	n/a	n/a
32	CEBPZ	chr3:75983702-75983951	HepG2	liver:	n/a	n/a
33	CHD1	chr3:76088184-76088476	H1-hESC	embryonic stem cell:	n/a	n/a
34	CHD1	chr3:76089070-76089144	H1-hESC	embryonic stem cell:	n/a	n/a
35	CHD2	chr3:76092684-76093435	H1-hESC	embryonic stem cell:	n/a	n/a
36	CHD2	chr3:76088171-76088769	H1-hESC	embryonic stem cell:	n/a	n/a
37	CHD2	chr3:75988257-75988329	GM12878	blood:	n/a	n/a
38	CREB1	chr3:76092854-76093434	H1-hESC	embryonic stem cell:	n/a	n/a
39	CTBP2	chr3:76092954-76093387	H1-hESC	embryonic stem cell:	n/a	n/a
40	CTCF	chr3:76094246-76094433	GM10266	blood:	n/a	chr3:76094319-76094337 chr3:76094314-76094335
41	CTCF	chr3:76094246-76094425	Pancreas_OC	pancreas:	n/a	chr3:76094319-76094337 chr3:76094314-76094335
42	CTCF	chr3:76094240-76094423	Kidney_OC	kidney:	n/a	chr3:76094319-76094337 chr3:76094314-76094335
43	CTCF	chr3:76082615-76082674	GM13976	blood:	n/a	n/a
44	CTCF	chr3:76094260-76094410	GM12873	blood:	n/a	chr3:76094319-76094337 chr3:76094314-76094335
45	CTCF	chr3:76073880-76074030	HEK293	kidney:	n/a	chr3:76073986-76074007 chr3:76073984-76074002
46	CTCF	chr3:76073820-76073970	GM12867	blood:	n/a	n/a
47	CTCF	chr3:76073925-76074099	HepG2	liver:	n/a	chr3:76073986-76074007 chr3:76073984-76074002
48	CTCF	chr3:76073900-76074050	HMF	breast:	n/a	chr3:76073986-76074007 chr3:76073984-76074002
49	CTCF	chr3:76094300-76094450	GM12871	blood:	n/a	chr3:76094319-76094337 chr3:76094314-76094335
50	CTCF	chr3:76073920-76074070	NB4	blood:	n/a	chr3:76073986-76074007 chr3:76073984-76074002

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:76076212-76076262	HIPEpiC	eye:	n/a
2	chr3:75958299-75958349	HRE	kidney:	n/a
3	chr3:76063500-76063550	HRPEpiC	eye:	n/a
4	chr3:76087918-76087968	MCF-7	breast:	n/a
5	chr3:76087918-76087968	HUVEC	blood vessel:	n/a
6	chr3:76063500-76063550	PANC-1	pancreas:	n/a
7	chr3:76063343-76063393	HRCEpiC	kidney:	n/a
8	chr3:76062325-76062375	Hepatocyte	liver:	n/a
9	chr3:76063500-76063550	HMEC	breast:	n/a
10	chr3:75958299-75958349	NHBE	bronchial:	n/a
11	chr3:76076212-76076262	NH-A	brain:	n/a
12	chr3:76062791-76062841	MCF10A-Er-Src	breast:	n/a
13	chr3:76076212-76076262	Hela-S3	cervix:	n/a
14	chr3:76087918-76087968	PFSK-1	brain:	n/a
15	chr3:76087918-76087968	HRE	kidney:	n/a
16	chr3:76087918-76087968	AG10803	skin:	n/a
17	chr3:76063500-76063550	BJ	skin:	n/a
18	chr3:76087918-76087968	PrEC	prostate:	n/a
19	chr3:76063343-76063393	GM12891	blood:	n/a
20	chr3:76076212-76076262	HepG2	liver:	n/a
21	chr3:76087918-76087968	Caco-2	colon:	n/a
22	chr3:75959386-75959436	Caco-2	colon:	n/a
23	chr3:75958299-75958349	Hepatocyte	liver:	n/a
24	chr3:76062325-76062375	IMR90	lung:	fetal
25	chr3:76062791-76062841	RPTEC	kidney:	n/a
26	chr3:76062791-76062841	NB4	blood:	n/a
27	chr3:76062791-76062841	LNCaP	prostate:	n/a
28	chr3:76087918-76087968	NT2-D1	testis:	n/a
29	chr3:75959386-75959436	GM19239	blood:	n/a
30	chr3:76062791-76062841	GM19239	blood:	n/a
31	chr3:76076212-76076262	AG04449	skin:	fetal
32	chr3:76062791-76062841	SK-N-SH_RA	brain:	n/a
33	chr3:76062791-76062841	GM06990	blood:	n/a
34	chr3:76063500-76063550	U87	brain:	n/a
35	chr3:75958299-75958349	GM12891	blood:	n/a
36	chr3:76062791-76062841	HMEC	breast:	n/a
37	chr3:76063500-76063550	GM12878	blood:	n/a
38	chr3:76063343-76063393	AG09309	skin:	n/a
39	chr3:76062325-76062375	MCF10A-Er-Src	breast:	n/a
40	chr3:76063500-76063550	Hepatocyte	liver:	n/a
41	chr3:75959386-75959436	Hepatocyte	liver:	n/a
42	chr3:75958299-75958349	HRCEpiC	kidney:	n/a
43	chr3:76063500-76063550	K562	blood:	n/a
44	chr3:76062325-76062375	A549	lung:	n/a
45	chr3:76062791-76062841	ProgFib	skin:	n/a
46	chr3:76076212-76076262	T-47D	breast:	n/a
47	chr3:76063343-76063393	NHBE	bronchial:	n/a
48	chr3:76063500-76063550	NHDF-neo	bronchial:	n/a
49	chr3:76063343-76063393	AoSMC	blood vessel:	n/a
50	chr3:76062325-76062375	HCM	heart:	n/a

No.	Distal block	Cell Line	Cell type
1	chr3:75867624..75868149-chr3:76093803..76094658,2	MCF-7	breast:
2	chr20:26208095..26209894-chr3:75988198..75990401,2	MCF-7	breast:
3	chr3:76073881..76074768-chr3:76093884..76094767,3	MCF-7	breast:
4	chr3:76077395..76079009-chr3:76080848..76082898,2	K562	blood:
5	chr3:76077395..76079009-chr3:76080848..76082898,2	K562	blood:
6	chr20:26199924..26201625-chr3:75995563..75997738,2	MCF-7	breast:
7	chr20:26206073..26206971-chr3:75991464..75992265,2	MCF-7	breast:
8	chr3:76073881..76074768-chr3:76093884..76094767,3	MCF-7	breast:
9	chr20:26201915..26204776-chr3:75992954..75996738,5	MCF-7	breast:
10	chr20:26208071..26209607-chr3:75987301..75988916,2	K562	blood:
11	chr20:26201563..26203476-chr3:75993448..75995749,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FRG2C-12	chr3:75986632-75986776	NONHSAT090553

Variant related genes	Relation type
ENSG00000222883	TF binding region
ENSG00000222883	CpG island

Extended variants
information (count: 2942 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:2942 , 50 per page) page: 1 2 3 4 5 6 7 ... 59

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs188044390	chr3:75958158-75958159	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs549732602	chr3:75958174-75958175	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs559235246	chr3:75958228-75958229	Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs149507122	chr3:75958292-75958293	Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs181213533	chr3:75958299-75958300	Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs560072107	chr3:75958367-75958368	Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs574790047	chr3:75958437-75958438	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs545891754	chr3:75958814-75958815	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs561593725	chr3:75958824-75958825	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs563969796	chr3:75958834-75958835	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs528257379	chr3:75958836-75958837	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs546506824	chr3:75958864-75958865	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs568238363	chr3:75958875-75958876	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs528886276	chr3:75958899-75958900	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs574345369	chr3:75958901-75958902	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs377384401	chr3:75958969-75958970	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs531735481	chr3:75963207-75963208	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs78421858	chr3:75963279-75963280	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs565270730	chr3:75963300-75963301	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs186420112	chr3:75963378-75963379	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs547890863	chr3:75963393-75963394	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs9310351	chr3:75963401-75963402	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
23	rs536025946	chr3:75963582-75963583	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs548485586	chr3:75963586-75963587	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs552866512	chr3:75963625-75963626	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs539060069	chr3:75963654-75963655	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs71315323	chr3:75963660-75963661	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs77614323	chr3:75963672-75963673	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs4856024	chr3:75963686-75963687	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
30	rs558168849	chr3:75963690-75963691	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs373680205	chr3:75963754-75963755	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs715468	chr3:75963778-75963779	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
33	rs552774401	chr3:75963787-75963788	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs555206084	chr3:75963852-75963853	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs572625054	chr3:75963859-75963860	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs144415817	chr3:75963887-75963888	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs188478353	chr3:75963925-75963926	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs576851127	chr3:75963947-75963948	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs111244966	chr3:75963966-75963967	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs565307991	chr3:75964064-75964065	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs532537342	chr3:75964089-75964090	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs568687626	chr3:75964120-75964121	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs185842005	chr3:75964193-75964194	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs565226040	chr3:75982407-75982408	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs564864840	chr3:75982432-75982433	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs34821214	chr3:75982494-75982495	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs142558887	chr3:75982547-75982548	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs7620543	chr3:75982552-75982553	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs184589190	chr3:75982583-75982584	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs190405422	chr3:75982603-75982604	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:83)

Disease	PMID	Source
Acute myeloid leukemia	20729466	CNVD
Glioblastoma multiforme	21080181	CNVD
Melanoma	18172304	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
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Esophageal cancer	20955586	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Acute myeloid leukemia	21251322	CNVD
Hirschsprung''s Disease	21712996	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21183584	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Bipolar disorder	20877625	CNVD
Bipolar disorder	21956041	CNVD
Bipolar disorder	22241247	CNVD
Biliary cancer	18923514	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Prostate cancer	21965145	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Cervical cancer	21062161	CNVD
Squamous cell cancer	20885788	CNVD
Autism	22102821	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Prostate cancer	18632612	CNVD
Metanephric adenoma	20802469	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21509527	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	21399695	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Colorectal cancer	16272173	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Soft tissue tumor	16732325	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Ovarian cancer	21720365	CNVD
Schizophrenia	20967226	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	21858162	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:281 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:75955400-75958400	Active TSS	Fetal Brain Female	brain
2	chr3:75958000-75958200	Enhancers	ES-I3 Cell Line	embryonic stem cell
3	chr3:75958400-75958600	Flanking Active TSS	Fetal Brain Female	brain
4	chr3:75958800-75959000	Enhancers	HUES64 Cell Line	embryonic stem cell
5	chr3:75963200-75964000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr3:75963600-75964200	Enhancers	iPS-15b Cell Line	embryonic stem cell
7	chr3:75964000-75964200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr3:75982400-75982600	Enhancers	HUES48 Cell Line	embryonic stem cell
9	chr3:75982400-75982600	Enhancers	HUES64 Cell Line	embryonic stem cell
10	chr3:75982600-75983200	Weak transcription	HUES64 Cell Line	embryonic stem cell
11	chr3:75982600-75983600	Weak transcription	HUES48 Cell Line	embryonic stem cell
12	chr3:75983200-75986800	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
13	chr3:75983600-75984600	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
14	chr3:75984800-75987000	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
15	chr3:75985000-75985400	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
16	chr3:75986400-75986800	ZNF genes & repeats	NHLF	lung
17	chr3:75986600-75986800	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr3:75986600-75986800	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
19	chr3:75986600-75986800	Enhancers	Esophagus	oesophagus
20	chr3:75986600-75986800	ZNF genes & repeats	Fetal Brain Male	brain
21	chr3:75986600-75986800	Enhancers	Gastric	stomach
22	chr3:75986600-75986800	ZNF genes & repeats	Pancreas	Pancrea
23	chr3:75986600-75986800	ZNF genes & repeats	Spleen	Spleen
24	chr3:75987200-75988200	Weak transcription	Fetal Brain Male	brain
25	chr3:75991000-75992000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr3:75994200-75996000	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
27	chr3:75994800-75996600	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
28	chr3:75995400-75995800	ZNF genes & repeats	Fetal Brain Male	brain
29	chr3:75998400-75998800	ZNF genes & repeats	Fetal Brain Male	brain
30	chr3:75998800-75999000	Weak transcription	Fetal Brain Male	brain
31	chr3:75999000-75999200	Enhancers	Fetal Brain Male	brain
32	chr3:75999400-76004200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
33	chr3:76017000-76017400	Enhancers	Fetal Brain Female	brain
34	chr3:76017400-76018400	Weak transcription	Fetal Brain Female	brain
35	chr3:76018400-76018600	Enhancers	Fetal Brain Female	brain
36	chr3:76032000-76033400	Enhancers	Fetal Brain Male	brain
37	chr3:76036400-76036800	Active TSS	Adipose Nuclei	Adipose
38	chr3:76041200-76042000	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
39	chr3:76041800-76042200	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
40	chr3:76043400-76044200	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
41	chr3:76059400-76059800	Enhancers	Adipose Nuclei	Adipose
42	chr3:76059400-76060600	Enhancers	Fetal Heart	heart
43	chr3:76060400-76060800	Enhancers	Left Ventricle	heart
44	chr3:76063600-76064200	Enhancers	Fetal Brain Male	brain
45	chr3:76064200-76065800	Weak transcription	Fetal Brain Male	brain
46	chr3:76065000-76066400	Enhancers	Fetal Brain Female	brain
47	chr3:76065800-76066200	Enhancers	Fetal Brain Male	brain
48	chr3:76065800-76066400	Enhancers	H9 Cell Line	embryonic stem cell
49	chr3:76066000-76066400	Enhancers	ES-I3 Cell Line	embryonic stem cell
50	chr3:76066200-76066600	Enhancers	HUES48 Cell Line	embryonic stem cell

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