Variant report

Variant	esv3349108
Chromosome Location	chr3:143676303-143692796
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1321)
CpG islands
(count:1405)
Chromatin interactive
region (count:39)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1321 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:143690119-143690425	HepG2	liver:	n/a	n/a
2	ARID3A	chr3:143692016-143692262	K562	blood:	n/a	n/a
3	ARID3A	chr3:143690276-143690865	K562	blood:	n/a	n/a
4	ATF1	chr3:143690072-143691003	K562	blood:	n/a	n/a
5	ATF1	chr3:143691998-143692250	K562	blood:	n/a	n/a
6	ATF2	chr3:143689546-143689945	GM12878	blood:	n/a	n/a
7	ATF2	chr3:143690518-143690969	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr3:143689642-143689972	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF2	chr3:143689985-143691159	GM12878	blood:	n/a	n/a
10	ATF2	chr3:143689913-143690495	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF2	chr3:143690239-143690706	GM12878	blood:	n/a	n/a
12	ATF2	chr3:143689986-143690694	H1-hESC	embryonic stem cell:	n/a	n/a
13	ATF2	chr3:143691190-143692375	GM12878	blood:	n/a	n/a
14	BACH1	chr3:143690053-143691021	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr3:143691840-143692192	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr3:143690304-143690487	K562	blood:	n/a	n/a
17	BACH1	chr3:143691359-143691614	H1-hESC	embryonic stem cell:	n/a	n/a
18	BATF	chr3:143690287-143690589	GM12878	blood:	n/a	n/a
19	BATF	chr3:143691917-143692241	GM12878	blood:	n/a	n/a
20	BCL3	chr3:143689933-143690628	A549	lung:	n/a	chr3:143690605-143690614
21	BCL3	chr3:143690183-143690968	A549	lung:	n/a	chr3:143690783-143690796 chr3:143690605-143690614
22	BCL3	chr3:143690035-143691020	GM12878	blood:	n/a	chr3:143690783-143690796 chr3:143690605-143690614
23	BCLAF1	chr3:143689915-143692474	GM12878	blood:	n/a	chr3:143690783-143690796 chr3:143690605-143690614 chr3:143691047-143691056
24	BCLAF1	chr3:143691843-143692343	GM12878	blood:	n/a	n/a
25	BHLHE40	chr3:143692346-143692846	HepG2	liver:	n/a	n/a
26	BHLHE40	chr3:143689623-143691632	GM12878	blood:	n/a	chr3:143691050-143691066
27	BHLHE40	chr3:143691295-143691495	A549	lung:	n/a	n/a
28	BHLHE40	chr3:143689620-143692459	K562	blood:	n/a	chr3:143691050-143691066
29	BHLHE40	chr3:143691990-143692386	GM12878	blood:	n/a	n/a
30	BRCA1	chr3:143690903-143690962	HepG2	liver:	n/a	n/a
31	BRCA1	chr3:143690389-143690910	GM12878	blood:	n/a	n/a
32	BRCA1	chr3:143689791-143689815	GM12878	blood:	n/a	n/a
33	BRCA1	chr3:143691819-143692647	Hela-S3	cervix:	n/a	n/a
34	BRCA1	chr3:143689916-143691085	Hela-S3	cervix:	n/a	n/a
35	BRCA1	chr3:143692161-143692163	GM12878	blood:	n/a	n/a
36	BRCA1	chr3:143690351-143690737	H1-hESC	embryonic stem cell:	n/a	n/a
37	BRCA1	chr3:143691742-143691775	GM12878	blood:	n/a	n/a
38	CBX3	chr3:143691226-143691772	K562	blood:	n/a	n/a
39	CBX3	chr3:143689868-143691100	K562	blood:	n/a	n/a
40	CBX3	chr3:143691884-143692323	K562	blood:	n/a	n/a
41	CCNT2	chr3:143689693-143692169	K562	blood:	n/a	chr3:143690254-143690263 chr3:143690184-143690193 chr3:143690620-143690629
42	CEBPB	chr3:143690809-143690964	H1-hESC	embryonic stem cell:	n/a	n/a
43	CEBPB	chr3:143690099-143690610	A549	lung:	n/a	n/a
44	CEBPB	chr3:143691170-143691347	H1-hESC	embryonic stem cell:	n/a	n/a
45	CEBPB	chr3:143690104-143691184	GM12878	blood:	n/a	n/a
46	CEBPB	chr3:143682853-143683052	A549	lung:	n/a	chr3:143682975-143682986
47	CEBPB	chr3:143690163-143690586	IMR90	lung:	n/a	n/a
48	CEBPB	chr3:143682909-143683058	HepG2	liver:	n/a	chr3:143682975-143682986
49	CEBPB	chr3:143690021-143692871	Hela-S3	cervix:	n/a	n/a
50	CEBPB	chr3:143690233-143690484	HepG2	liver:	n/a	n/a

(count:1405 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:143689972-143690022	NT2-D1	testis:	n/a
2	chr3:143692134-143692184	GM12878	blood:	n/a
3	chr3:143689972-143690022	NT2-D1	testis:	n/a
4	chr3:143692134-143692184	GM12878	blood:	n/a
5	chr3:143690741-143690791	HMEC	breast:	n/a
6	chr3:143692056-143692106	AG09309	skin:	n/a
7	chr3:143689584-143689634	H1-hESC	embryonic stem cell:	embryo
8	chr3:143692146-143692196	H1-hESC	embryonic stem cell:	embryo
9	chr3:143692134-143692184	Hepatocyte	liver:	n/a
10	chr3:143690145-143690195	HMEC	breast:	n/a
11	chr3:143689916-143689966	HRCEpiC	kidney:	n/a
12	chr3:143692056-143692106	AG09319	gingival:	n/a
13	chr3:143692320-143692370	K562	blood:	n/a
14	chr3:143692255-143692305	RPTEC	kidney:	n/a
15	chr3:143689584-143689634	PFSK-1	brain:	n/a
16	chr3:143692056-143692106	HMEC	breast:	n/a
17	chr3:143690493-143690543	IMR90	lung:	fetal
18	chr3:143690928-143690978	NB4	blood:	n/a
19	chr3:143690246-143690296	ECC-1	luminal epithelium:	n/a
20	chr3:143692785-143692835	AoSMC	blood vessel:	n/a
21	chr3:143692146-143692196	ECC-1	luminal epithelium:	n/a
22	chr3:143692006-143692056	AG04450	lung:	fetal
23	chr3:143692255-143692305	AG09309	skin:	n/a
24	chr3:143692785-143692835	NHDF-neo	bronchial:	n/a
25	chr3:143690495-143690545	HPAEpiC	pulmonary alveolar:	n/a
26	chr3:143690991-143691041	ovcar-3	ovarian:	n/a
27	chr3:143692134-143692184	ovcar-3	ovarian:	n/a
28	chr3:143690246-143690296	HL-60	blood:	n/a
29	chr3:143689972-143690022	AG09319	gingival:	n/a
30	chr3:143690208-143690258	BE2_C	brain:	n/a
31	chr3:143690246-143690296	Hela-S3	cervix:	n/a
32	chr3:143690741-143690791	IMR90	lung:	fetal
33	chr3:143689972-143690022	NH-A	brain:	n/a
34	chr3:143692320-143692370	IMR90	lung:	fetal
35	chr3:143692087-143692137	ECC-1	luminal epithelium:	n/a
36	chr3:143691409-143691459	AG09319	gingival:	n/a
37	chr3:143690991-143691041	LNCaP	prostate:	n/a
38	chr3:143692255-143692305	BE2_C	brain:	n/a
39	chr3:143692320-143692370	AG04450	lung:	fetal
40	chr3:143692134-143692184	AG04450	lung:	fetal
41	chr3:143690991-143691041	HNPCEpiC	eye:	n/a
42	chr3:143690991-143691041	AG09309	skin:	n/a
43	chr3:143691269-143691319	AG04449	skin:	fetal
44	chr3:143689972-143690022	HepG2	liver:	n/a
45	chr3:143691409-143691459	AoSMC	blood vessel:	n/a
46	chr3:143692006-143692056	HEK293	kidney:	embryo
47	chr3:143690991-143691041	U87	brain:	n/a
48	chr3:143692785-143692835	MCF10A-Er-Src	breast:	n/a
49	chr3:143690246-143690296	HNPCEpiC	eye:	n/a
50	chr3:143689810-143689860	GM12892	blood:	n/a

(count:39 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:143690746..143691426-chr7:26239897..26240781,2	Hela-S3	cervix:
2	chr3:143687536..143689056-chr3:143689809..143691733,2	MCF-7	breast:
3	chr3:143676128..143679068-chr3:143689463..143692123,2	K562	blood:
4	chr3:143679544..143684036-chr3:143688020..143692535,7	MCF-7	breast:
5	chr11:17097769..17100478-chr3:143690055..143692307,2	MCF-7	breast:
6	chr17:25621104..25621916-chr3:143690294..143691222,2	Hela-S3	cervix:
7	chr3:143676919..143679412-chr3:143688995..143692223,3	MCF-7	breast:
8	chr17:57914617..57916585-chr3:143689584..143691332,2	MCF-7	breast:
9	chr12:92539191..92539985-chr3:143690264..143691024,2	Hela-S3	cervix:
10	chr12:16064190..16064741-chr3:143690280..143690998,2	Hela-S3	cervix:
11	chr3:143677587..143679390-chr3:143686141..143687965,2	MCF-7	breast:
12	chr19:57831383..57832246-chr3:143690551..143691404,2	NB4	blood:
13	chr3:143680103..143683758-chr3:143690045..143692584,4	MCF-7	breast:
14	chr3:143690723..143691617-chr6:74230015..74230752,2	Hela-S3	cervix:
15	chr3:143566553..143569042-chr3:143690803..143692633,2	MCF-7	breast:
16	chr11:85375642..85376556-chr3:143690557..143691172,2	Hela-S3	cervix:
17	chr3:143690837..143691539-chr4:113066463..113067171,2	Hela-S3	cervix:
18	chr3:143688929..143690453-chr9:116724811..116727064,2	MCF-7	breast:
19	chr22:19418740..19420583-chr3:143689830..143691587,2	MCF-7	breast:
20	chr16:28857621..28858218-chr3:143690524..143691094,2	Hela-S3	cervix:
21	chr3:143674855..143677233-chr3:143692138..143694491,2	K562	blood:
22	chr19:44258720..44259380-chr3:143690069..143691057,2	Hela-S3	cervix:
23	chr2:88315349..88316190-chr3:143690878..143691682,2	HCT-116	colon:
24	chr16:88876624..88878169-chr3:143691035..143693133,2	MCF-7	breast:
25	chr3:143674139..143676355-chr3:143690634..143693638,3	K562	blood:
26	chr3:143684124..143687534-chr3:143688769..143693859,7	MCF-7	breast:
27	chr12:49524816..49525687-chr3:143690429..143691195,2	Hela-S3	cervix:
28	chr3:112280243..112281155-chr3:143690900..143691448,2	Hela-S3	cervix:
29	chr3:143689777..143690496-chr6:26055384..26056279,2	Hela-S3	cervix:
30	chr3:143692106..143692865-chr7:112090373..112091302,2	Hela-S3	cervix:
31	chr11:65625345..65626177-chr3:143690525..143691289,2	Hela-S3	cervix:
32	chr3:143689763..143690371-chr7:23510326..23510860,2	Hela-S3	cervix:
33	chr19:18682649..18683371-chr3:143690264..143691172,2	Hela-S3	cervix:
34	chr3:143677587..143679390-chr3:143686141..143687965,2	MCF-7	breast:
35	chr3:143690729..143691347-chr6:35656198..35657113,2	Hela-S3	cervix:
36	chr10:98592013..98592977-chr3:143690256..143690764,2	Hela-S3	cervix:
37	chr3:143689958..143690542-chr6:44224790..44225315,2	Hela-S3	cervix:
38	chr16:87425040..87425562-chr3:143690703..143691313,2	Hela-S3	cervix:
39	chr12:12956339..12957122-chr3:143689535..143690489,2	Hela-S3	cervix:

No data

Variant related genes	Relation type
C3orf58	TF binding region
C3orf58	CpG island
ENSG00000140941	chromatin interactions
ENSG00000109046	chromatin interactions
ENSG00000181804	chromatin interactions
ENSG00000023697	chromatin interactions
ENSG00000138459	chromatin interactions
ENSG00000133639	chromatin interactions
ENSG00000110700	chromatin interactions
ENSG00000174749	chromatin interactions
ENSG00000178188	chromatin interactions
ENSG00000245904	chromatin interactions
ENSG00000185608	chromatin interactions
ENSG00000105771	chromatin interactions
ENSG00000137504	chromatin interactions
ENSG00000062716	chromatin interactions
ENSG00000172757	chromatin interactions
ENSG00000122566	chromatin interactions
ENSG00000181744	chromatin interactions
ENSG00000156508	chromatin interactions
ENSG00000157593	chromatin interactions
ENSG00000178952	chromatin interactions
ENSG00000123416	chromatin interactions
ENSG00000198931	chromatin interactions
ENSG00000221983	chromatin interactions
ENSG00000222724	chromatin interactions
ENSG00000096060	chromatin interactions
ENSG00000258017	chromatin interactions
ENSG00000196233	chromatin interactions
ENSG00000100084	chromatin interactions
ENSG00000006652	chromatin interactions
ENSG00000178229	chromatin interactions
ENSG00000144848	chromatin interactions

Extended variants
information (count: 657 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:657 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs145039060	chr3:143676317-143676318	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs549595229	chr3:143676330-143676331	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs567757148	chr3:143676351-143676352	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs534988140	chr3:143676362-143676363	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs7626898	chr3:143676375-143676376	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs567296409	chr3:143676582-143676583	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs144684293	chr3:143676589-143676590	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs57506012	chr3:143676598-143676599	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs144419787	chr3:143676624-143676625	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs202233341	chr3:143676628-143676629	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs577234225	chr3:143676644-143676645	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs568732456	chr3:143676659-143676660	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs373491900	chr3:143676694-143676695	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs190831427	chr3:143676775-143676776	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs35594399	chr3:143676859-143676860	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs34294088	chr3:143676861-143676862	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs570008413	chr3:143676863-143676864	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs542345965	chr3:143676867-143676868	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs35928435	chr3:143676898-143676899	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs183388188	chr3:143676917-143676918	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs573035425	chr3:143676922-143676923	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs149140126	chr3:143676990-143676991	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs386666620	chr3:143677053-143677054	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs532428467	chr3:143677061-143677062	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs187278620	chr3:143677063-143677064	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs9872448	chr3:143677073-143677074	Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs531082626	chr3:143677075-143677076	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs201801238	chr3:143677076-143677077	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs9854844	chr3:143677083-143677084	Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs567856828	chr3:143677115-143677116	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs193162886	chr3:143677117-143677118	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs546910982	chr3:143677176-143677177	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs9872595	chr3:143677179-143677180	Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs538928952	chr3:143677180-143677181	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs556954886	chr3:143677220-143677221	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs75247103	chr3:143677241-143677242	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs536357734	chr3:143677249-143677250	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs184557685	chr3:143677264-143677265	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs201201317	chr3:143677276-143677277	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs199535181	chr3:143677277-143677278	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs34372926	chr3:143677278-143677279	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs71304252	chr3:143677280-143677281	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs78517371	chr3:143677281-143677282	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs60043700	chr3:143677285-143677286	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs78385247	chr3:143677334-143677335	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs188249366	chr3:143677396-143677397	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs146462169	chr3:143677422-143677423	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs78490098	chr3:143677436-143677437	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs577251096	chr3:143677437-143677438	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs1370027	chr3:143677458-143677459	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:55)

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
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
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	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
microdeletion syndrome	22180640	CNVD
Basal cell lymphoma	21115979	CNVD
Ovarian cancer	22174824	CNVD
Colorectal cancer	18645599	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Hepatocellular carcinoma	16750200	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myelodysplastic syndrome	21251322	CNVD
Blepharophimosis-ptosis-epicanthus inversus syndrome	22067867	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
abnormal development	18461090	CNVD
Cancer	21129771	CNVD
Ovarian cancer	23621864	CNVD
Breast cancer	21364760	CNVD
Mental retardation	17847001	CNVD
Basal cell lymphoma	17170743	CNVD
Adrenocortical carcinoma	18281524	CNVD
Breast cancer	21509527	CNVD
Congenital anomalies of the kidney and urinary tract	20605837	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:335 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:143674000-143676400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
2	chr3:143675200-143676400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
3	chr3:143675400-143676400	Enhancers	Primary T killer memory cells from peripheral blood	blood
4	chr3:143675400-143676600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
5	chr3:143675400-143676600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr3:143675600-143676400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
7	chr3:143675800-143676400	Enhancers	Primary T helper cells fromperipheralblood	blood
8	chr3:143675800-143676800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
9	chr3:143676000-143676400	Enhancers	Primary T helper cells PMA-I stimulated	--
10	chr3:143676000-143677000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
11	chr3:143676000-143677200	Enhancers	Primary T helper naive cells from peripheral blood	blood
12	chr3:143676200-143676600	Enhancers	Primary T regulatory cells fromperipheralblood	blood
13	chr3:143676400-143677000	Enhancers	Primary hematopoietic stem cells short term culture	blood
14	chr3:143680400-143689600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr3:143681800-143682000	Bivalent Enhancer	Left Ventricle	heart
16	chr3:143682000-143682200	Enhancers	H9 Cell Line	embryonic stem cell
17	chr3:143682200-143682800	Enhancers	HUES48 Cell Line	embryonic stem cell
18	chr3:143682200-143683800	Weak transcription	Pancreas	Pancrea
19	chr3:143682400-143683000	Enhancers	iPS-15b Cell Line	embryonic stem cell
20	chr3:143682400-143683400	Enhancers	Primary monocytes fromperipheralblood	blood
21	chr3:143682400-143683400	Enhancers	Monocytes-CD14+_RO01746	blood
22	chr3:143682600-143683200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr3:143682600-143685000	Weak transcription	H9 Cell Line	embryonic stem cell
24	chr3:143682800-143688800	Weak transcription	HUES48 Cell Line	embryonic stem cell
25	chr3:143683400-143689200	Weak transcription	Monocytes-CD14+_RO01746	blood
26	chr3:143683600-143684000	Enhancers	Osteobl	bone
27	chr3:143683800-143684000	ZNF genes & repeats	Pancreas	Pancrea
28	chr3:143683800-143689400	Weak transcription	Brain Substantia Nigra	brain
29	chr3:143684000-143689600	Weak transcription	Pancreas	Pancrea
30	chr3:143685000-143685200	Enhancers	H9 Cell Line	embryonic stem cell
31	chr3:143685000-143685600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr3:143685200-143685400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr3:143685200-143685400	Enhancers	HSMMtube	muscle
34	chr3:143685200-143689600	Weak transcription	H9 Cell Line	embryonic stem cell
35	chr3:143685600-143688800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr3:143685600-143689000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr3:143687600-143689400	Weak transcription	Right Atrium	heart
38	chr3:143687800-143688000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
39	chr3:143688000-143689600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
40	chr3:143688800-143689000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr3:143688800-143689000	Enhancers	Primary hematopoietic stem cells short term culture	blood
42	chr3:143688800-143689000	Bivalent Enhancer	Dnd41	blood
43	chr3:143688800-143689200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr3:143688800-143689200	Enhancers	HUES48 Cell Line	embryonic stem cell
45	chr3:143688800-143689200	Enhancers	iPS-18 Cell Line	embryonic stem cell
46	chr3:143688800-143689200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
47	chr3:143688800-143689200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr3:143688800-143689400	Enhancers	Primary hematopoietic stem cells	blood
49	chr3:143688800-143689400	Enhancers	Colon Smooth Muscle	Colon
50	chr3:143688800-143696400	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain

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