Variant report

Variant	nsv998740
Chromosome Location	chr3:121289499-121390271
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:762)
CpG islands
(count:916)
Chromatin interactive
region (count:22)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:762 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:121293415-121293609	HepG2	liver:	n/a	n/a
2	ARID3A	chr3:121316361-121316430	K562	blood:	n/a	n/a
3	ARID3A	chr3:121361606-121361746	HepG2	liver:	n/a	n/a
4	ARID3A	chr3:121316377-121316483	HepG2	liver:	n/a	n/a
5	ARID3A	chr3:121293291-121293628	K562	blood:	n/a	n/a
6	ATF1	chr3:121293341-121293636	K562	blood:	n/a	n/a
7	ATF2	chr3:121379094-121380020	GM12878	blood:	n/a	n/a
8	ATF2	chr3:121311633-121312689	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF2	chr3:121311674-121312713	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF2	chr3:121379019-121380056	GM12878	blood:	n/a	n/a
11	ATF2	chr3:121373211-121373782	GM12878	blood:	n/a	n/a
12	ATF3	chr3:121293358-121293722	K562	blood:	n/a	n/a
13	ATF3	chr3:121312116-121312453	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr3:121293357-121293710	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr3:121370532-121370903	K562	blood:	n/a	n/a
16	BACH1	chr3:121311672-121312712	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr3:121370567-121370886	H1-hESC	embryonic stem cell:	n/a	n/a
18	BATF	chr3:121373309-121373740	GM12878	blood:	n/a	n/a
19	BATF	chr3:121373310-121373733	GM12878	blood:	n/a	n/a
20	BCLAF1	chr3:121378976-121380116	GM12878	blood:	n/a	n/a
21	BCLAF1	chr3:121373280-121373842	GM12878	blood:	n/a	n/a
22	BCLAF1	chr3:121373301-121373736	GM12878	blood:	n/a	n/a
23	BCLAF1	chr3:121379038-121380039	GM12878	blood:	n/a	n/a
24	BHLHE40	chr3:121356973-121357138	GM12878	blood:	n/a	n/a
25	CBX3	chr3:121293244-121293683	K562	blood:	n/a	n/a
26	CCNT2	chr3:121373404-121373517	K562	blood:	n/a	n/a
27	CEBPB	chr3:121309763-121310107	HepG2	liver:	n/a	chr3:121309917-121309928
28	CEBPB	chr3:121373937-121374111	HepG2	liver:	n/a	chr3:121374048-121374059 chr3:121374047-121374060 chr3:121374047-121374060 chr3:121374049-121374058 chr3:121374047-121374058
29	CEBPB	chr3:121361452-121361746	HepG2	liver:	n/a	n/a
30	CEBPB	chr3:121316268-121316598	HepG2	liver:	n/a	n/a
31	CEBPB	chr3:121360050-121360315	IMR90	lung:	n/a	n/a
32	CEBPB	chr3:121373910-121374202	A549	lung:	n/a	chr3:121374048-121374059 chr3:121374047-121374060 chr3:121374047-121374060 chr3:121374049-121374058 chr3:121374047-121374058
33	CEBPB	chr3:121291437-121291752	HepG2	liver:	n/a	chr3:121291589-121291600
34	CEBPB	chr3:121373910-121374225	Hela-S3	cervix:	n/a	chr3:121374048-121374059 chr3:121374047-121374060 chr3:121374047-121374060 chr3:121374049-121374058 chr3:121374047-121374058
35	CEBPB	chr3:121316419-121316506	K562	blood:	n/a	n/a
36	CEBPB	chr3:121360040-121360324	K562	blood:	n/a	n/a
37	CEBPB	chr3:121293333-121293620	K562	blood:	n/a	n/a
38	CEBPB	chr3:121309772-121310101	IMR90	lung:	n/a	chr3:121309917-121309928
39	CEBPB	chr3:121373866-121374236	HepG2	liver:	n/a	chr3:121374048-121374059 chr3:121374047-121374060 chr3:121374047-121374060 chr3:121374049-121374058 chr3:121374047-121374058
40	CEBPB	chr3:121361504-121361673	HepG2	liver:	n/a	n/a
41	CEBPB	chr3:121316313-121316588	Hela-S3	cervix:	n/a	n/a
42	CEBPB	chr3:121309777-121310035	K562	blood:	n/a	chr3:121309917-121309928
43	CEBPB	chr3:121312150-121312397	K562	blood:	n/a	n/a
44	CEBPB	chr3:121373885-121374223	IMR90	lung:	n/a	chr3:121374048-121374059 chr3:121374047-121374060 chr3:121374047-121374060 chr3:121374049-121374058 chr3:121374047-121374058
45	CEBPB	chr3:121360036-121360299	A549	lung:	n/a	n/a
46	CEBPB	chr3:121312057-121312606	H1-hESC	embryonic stem cell:	n/a	n/a
47	CEBPB	chr3:121316303-121316542	IMR90	lung:	n/a	n/a
48	CEBPB	chr3:121309775-121310048	A549	lung:	n/a	chr3:121309917-121309928
49	CEBPB	chr3:121378977-121380300	GM12878	blood:	n/a	chr3:121379054-121379065
50	CEBPB	chr3:121312115-121312384	HepG2	liver:	n/a	n/a

(count:916 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:121379791-121379841	AG04449	skin:	fetal
2	chr3:121379791-121379841	AG04449	skin:	fetal
3	chr3:121380236-121380286	HUVEC	blood vessel:	n/a
4	chr3:121348609-121348659	LNCaP	prostate:	n/a
5	chr3:121310923-121310973	PrEC	prostate:	n/a
6	chr3:121380792-121380842	SK-N-SH_RA	brain:	n/a
7	chr3:121311075-121311125	HRE	kidney:	n/a
8	chr3:121379777-121379827	HepG2	liver:	n/a
9	chr3:121380792-121380842	HIPEpiC	eye:	n/a
10	chr3:121379745-121379795	CMK	blood:	n/a
11	chr3:121312241-121312291	ProgFib	skin:	n/a
12	chr3:121312127-121312177	HIPEpiC	eye:	n/a
13	chr3:121379745-121379795	Hepatocyte	liver:	n/a
14	chr3:121307887-121307937	Jurkat	blood:	n/a
15	chr3:121312127-121312177	AG04449	skin:	fetal
16	chr3:121379745-121379795	HNPCEpiC	eye:	n/a
17	chr3:121307887-121307937	U87	brain:	n/a
18	chr3:121311075-121311125	HEEpiC	esophagus:	n/a
19	chr3:121311075-121311125	SKMC	muscle:	n/a
20	chr3:121312164-121312214	HL-60	blood:	n/a
21	chr3:121379745-121379795	MCF-7	breast:	n/a
22	chr3:121312127-121312177	HEK293	kidney:	embryo
23	chr3:121380236-121380286	ProgFib	skin:	n/a
24	chr3:121312127-121312177	NH-A	brain:	n/a
25	chr3:121312164-121312214	HepG2	liver:	n/a
26	chr3:121312164-121312214	HEEpiC	esophagus:	n/a
27	chr3:121380792-121380842	HCF	heart:	n/a
28	chr3:121379791-121379841	MCF-7	breast:	n/a
29	chr3:121312164-121312214	GM12891	blood:	n/a
30	chr3:121379745-121379795	SKMC	muscle:	n/a
31	chr3:121380236-121380286	SK-N-SH	brain:	n/a
32	chr3:121312241-121312291	NHBE	bronchial:	n/a
33	chr3:121312127-121312177	NHDF-neo	bronchial:	n/a
34	chr3:121363104-121363154	SK-N-SH_RA	brain:	n/a
35	chr3:121380236-121380286	Caco-2	colon:	n/a
36	chr3:121348609-121348659	ovcar-3	ovarian:	n/a
37	chr3:121311075-121311125	BE2_C	brain:	n/a
38	chr3:121380792-121380842	ECC-1	luminal epithelium:	n/a
39	chr3:121379777-121379827	BJ	skin:	n/a
40	chr3:121312127-121312177	HRPEpiC	eye:	n/a
41	chr3:121312127-121312177	LNCaP	prostate:	n/a
42	chr3:121312164-121312214	AoSMC	blood vessel:	n/a
43	chr3:121348609-121348659	AG04449	skin:	fetal
44	chr3:121312127-121312177	AoSMC	blood vessel:	n/a
45	chr3:121380236-121380286	CMK	blood:	n/a
46	chr3:121311075-121311125	K562	blood:	n/a
47	chr3:121310923-121310973	GM12891	blood:	n/a
48	chr3:121380236-121380286	HEEpiC	esophagus:	n/a
49	chr3:121307887-121307937	BJ	skin:	n/a
50	chr3:121363104-121363154	SK-N-SH	brain:	n/a

(count:22 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:121381533..121383209-chr3:121385289..121388100,2	MCF-7	breast:
2	chr3:121378883..121381780-chr3:121382077..121384890,2	K562	blood:
3	chr17:60095074..60095939-chr3:121314935..121315693,2	MCF-7	breast:
4	chr3:121325183..121326691-chr3:121327746..121330379,2	K562	blood:
5	chr3:121384342..121386908-chr3:121387953..121390169,2	K562	blood:
6	chr3:121291865..121293689-chr3:121466098..121468278,2	K562	blood:
7	chr1:151043136..151043657-chr3:121379199..121379950,2	NB4	blood:
8	chr3:121339257..121341104-chr3:121379300..121381638,2	K562	blood:
9	chr3:121344119..121346108-chr3:121348732..121350963,2	K562	blood:
10	chr3:121355706..121357313-chr3:121467523..121469117,2	K562	blood:
11	chr3:121361933..121363730-chr3:121367165..121368759,2	K562	blood:
12	chr3:121288728..121291116-chr3:121291333..121293786,2	MCF-7	breast:
13	chr3:121325183..121326691-chr3:121327746..121330379,2	K562	blood:
14	chr3:121381533..121383209-chr3:121385289..121388100,2	MCF-7	breast:
15	chr3:121298924..121301111-chr3:121307868..121309748,2	MCF-7	breast:
16	chr3:121298924..121301111-chr3:121307868..121309748,2	MCF-7	breast:
17	chr3:121374281..121376977-chr3:121381116..121385045,3	MCF-7	breast:
18	chr3:121380202..121382389-chr3:121387909..121390057,2	K562	blood:
19	chr3:121384342..121386908-chr3:121387953..121390169,2	K562	blood:
20	chr3:121380202..121382389-chr3:121387909..121390057,2	K562	blood:
21	chr3:121344119..121346108-chr3:121348732..121350963,2	K562	blood:
22	chr3:121377179..121379153-chr3:121573085..121574882,2	MCF-7	breast:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GOLGB1-1	chr3:121376829-121377194	NONHSAT091478
2	lnc-GOLGB1-1	chr3:121379667-121379750	NONHSAT091478
3	lnc-POLQ-1	chr3:121295924-121296127	expReg_chr3_8545_-
4	lnc-GOLGB1-2	chr3:121372843-121373143	NONHSAT091474

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	GOLGB1	hsa-miR-197-3p	chr3:121382120-121382141
2	GOLGB1	hsa-miR-197-3p	chr3:121382796-121382817

Variant related genes	Relation type
ENSG00000238670	TF binding region
RNU4-62P	TF binding region
RN7SL172P	TF binding region
HCLS1	TF binding region
ARGFX	TF binding region
FBXO40	TF binding region
ENSG00000238670	CpG island
RNU4-62P	CpG island
RN7SL172P	CpG island
HCLS1	CpG island
ARGFX	CpG island
FBXO40	CpG island
ENSG00000180353	chromatin interactions
ENSG00000173230	chromatin interactions
ENSG00000143458	chromatin interactions
ENSG00000222057	chromatin interactions
ENSG00000186103	chromatin interactions

Extended variants
information (count: 3941 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:3941 , 50 per page) page: 1 2 3 4 5 6 7 ... 79

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12485719	chr3:121289499-121289500	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs546174245	chr3:121289503-121289504	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs77686228	chr3:121289532-121289533	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs200448128	chr3:121289569-121289570	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs147644178	chr3:121289594-121289595	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs202191342	chr3:121289604-121289605	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs201721488	chr3:121289614-121289615	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs147017228	chr3:121289627-121289628	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs188489586	chr3:121289628-121289629	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs543287924	chr3:121289629-121289630	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs529810537	chr3:121289634-121289635	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs561329789	chr3:121289654-121289655	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs201565904	chr3:121289655-121289656	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs145075970	chr3:121289661-121289662	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs200957471	chr3:121289687-121289688	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs371398266	chr3:121289703-121289704	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs532276032	chr3:121289752-121289753	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs80011604	chr3:121289778-121289779	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs568820336	chr3:121289804-121289805	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs531236513	chr3:121289813-121289814	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs9812322	chr3:121289829-121289830	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs372057835	chr3:121290001-121290002	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs568081244	chr3:121290011-121290012	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs534351805	chr3:121290041-121290042	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs76617032	chr3:121290048-121290049	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs78685351	chr3:121290176-121290177	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs540125935	chr3:121290190-121290191	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs145348939	chr3:121290213-121290214	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs192844458	chr3:121290247-121290248	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs112296053	chr3:121290253-121290254	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs6771845	chr3:121290280-121290281	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs182604208	chr3:121290376-121290377	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs139923317	chr3:121290400-121290401	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs374256491	chr3:121290401-121290402	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs541879225	chr3:121290420-121290421	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs539622205	chr3:121290421-121290422	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs186466139	chr3:121290423-121290424	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs536150743	chr3:121290424-121290425	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs3079740	chr3:121290425-121290426	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs376594680	chr3:121290426-121290427	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs35055897	chr3:121290427-121290428	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs572216008	chr3:121290501-121290502	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs537407288	chr3:121290503-121290504	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs370346743	chr3:121290547-121290548	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs28619898	chr3:121290602-121290603	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs13319094	chr3:121290604-121290605	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs13319095	chr3:121290606-121290607	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs9755075	chr3:121290638-121290639	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs532210442	chr3:121290644-121290645	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs546057068	chr3:121290658-121290659	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:68)

Disease	PMID	Source
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	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
Prostate cancer	21965145	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Cervical cancer	21062161	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
microdeletion syndrome	22180640	CNVD
Cervical Cancer	21857958	CNVD
Melanoma	21693616	CNVD
Lung cancer	21426551	CNVD
Cancer	21637783	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oral cancer	21386901	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	22065749	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	16608533	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Developmental delay	22180640	CNVD
Multiple myeloma	17550852	CNVD
Basal cell lymphoma	21115979	CNVD
Ovarian cancer	22174824	CNVD
lymphocytic leukemia	21291569	CNVD
small cell lung cancer	20016488	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Autism	22241247	CNVD
Pancreatic cancer	17952125	CNVD
Bipolar disorder	17953491	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
early-passage human iPS cells	21368824	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1491 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:121283800-121293400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr3:121289000-121289600	Enhancers	H1 Cell Line	embryonic stem cell
3	chr3:121289000-121289800	Enhancers	H9 Cell Line	embryonic stem cell
4	chr3:121289000-121289800	Enhancers	HUES48 Cell Line	embryonic stem cell
5	chr3:121289000-121289800	Enhancers	HUES6 Cell Line	embryonic stem cell
6	chr3:121289000-121290000	Enhancers	HUES64 Cell Line	embryonic stem cell
7	chr3:121289000-121290000	Enhancers	iPS-18 Cell Line	embryonic stem cell
8	chr3:121289200-121290000	Enhancers	ES-I3 Cell Line	embryonic stem cell
9	chr3:121289200-121290000	Enhancers	iPS-15b Cell Line	embryonic stem cell
10	chr3:121289200-121290000	Enhancers	iPS-20b Cell Line	embryonic stem cell
11	chr3:121289600-121293200	Weak transcription	H1 Cell Line	embryonic stem cell
12	chr3:121289800-121293200	Weak transcription	H9 Cell Line	embryonic stem cell
13	chr3:121289800-121293400	Weak transcription	HUES6 Cell Line	embryonic stem cell
14	chr3:121290000-121293400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
15	chr3:121290000-121293600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
16	chr3:121292800-121293000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr3:121292800-121293800	Enhancers	K562	blood
18	chr3:121293200-121293600	Enhancers	H1 Cell Line	embryonic stem cell
19	chr3:121293200-121293600	Enhancers	H9 Cell Line	embryonic stem cell
20	chr3:121293400-121293600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr3:121293400-121293800	Enhancers	ES-I3 Cell Line	embryonic stem cell
22	chr3:121293400-121293800	Enhancers	HUES6 Cell Line	embryonic stem cell
23	chr3:121293400-121293800	Enhancers	A549	lung
24	chr3:121293400-121293800	Enhancers	Hela-S3	cervix
25	chr3:121293400-121294400	Enhancers	Fetal Heart	heart
26	chr3:121293600-121293800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr3:121293600-121294000	Bivalent Enhancer	ES-WA7 Cell Line	embryonic stem cell
28	chr3:121293600-121294000	Enhancers	iPS-15b Cell Line	embryonic stem cell
29	chr3:121293600-121311800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr3:121297600-121297800	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
31	chr3:121297600-121297800	Enhancers	Pancreas	Pancrea
32	chr3:121297800-121300600	Weak transcription	Pancreas	Pancrea
33	chr3:121300600-121300800	Enhancers	Pancreas	Pancrea
34	chr3:121302400-121302600	Enhancers	Pancreas	Pancrea
35	chr3:121302800-121303400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
36	chr3:121303400-121303600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
37	chr3:121303400-121303800	Enhancers	iPS-15b Cell Line	embryonic stem cell
38	chr3:121303400-121304000	Enhancers	ES-I3 Cell Line	embryonic stem cell
39	chr3:121303800-121310400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
40	chr3:121304000-121309000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
41	chr3:121305800-121309000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
42	chr3:121309000-121309200	Enhancers	HUES64 Cell Line	embryonic stem cell
43	chr3:121309000-121309200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
44	chr3:121309000-121311600	Enhancers	ES-I3 Cell Line	embryonic stem cell
45	chr3:121309200-121310600	Weak transcription	HUES64 Cell Line	embryonic stem cell
46	chr3:121309200-121311600	Enhancers	iPS-18 Cell Line	embryonic stem cell
47	chr3:121309200-121311600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
48	chr3:121309200-121311800	Enhancers	HUES48 Cell Line	embryonic stem cell
49	chr3:121309400-121310600	Enhancers	iPS-20b Cell Line	embryonic stem cell
50	chr3:121310000-121310200	Enhancers	H1 Cell Line	embryonic stem cell

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