Variant report

Variant	esv3417076
Chromosome Location	chr3:56590062-56591960
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:594)
CpG islands
(count:549)
Chromatin interactive
region (count:10)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:594 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:56591600-56592272	HepG2	liver:	n/a	n/a
2	ARID3A	chr3:56590851-56591380	HepG2	liver:	n/a	n/a
3	ARID3A	chr3:56591601-56592288	K562	blood:	n/a	n/a
4	ATF2	chr3:56591486-56591946	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr3:56590824-56591220	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr3:56590933-56590950	H1-hESC	embryonic stem cell:	n/a	n/a
7	BCLAF1	chr3:56590884-56591283	GM12878	blood:	n/a	n/a
8	BHLHE40	chr3:56590970-56591312	GM12878	blood:	n/a	n/a
9	BHLHE40	chr3:56590983-56591813	K562	blood:	n/a	n/a
10	BRCA1	chr3:56590978-56591890	Hela-S3	cervix:	n/a	n/a
11	BRCA1	chr3:56591027-56591163	H1-hESC	embryonic stem cell:	n/a	n/a
12	CBX3	chr3:56591069-56591526	K562	blood:	n/a	n/a
13	CBX3	chr3:56590923-56591423	K562	blood:	n/a	n/a
14	CCNT2	chr3:56590957-56591472	K562	blood:	n/a	n/a
15	CEBPB	chr3:56590685-56592055	Hela-S3	cervix:	n/a	chr3:56591677-56591694
16	CEBPB	chr3:56590587-56591851	K562	blood:	n/a	chr3:56591677-56591694
17	CEBPB	chr3:56590910-56591868	IMR90	lung:	n/a	chr3:56591677-56591694
18	CEBPB	chr3:56590919-56591278	HepG2	liver:	n/a	n/a
19	CEBPB	chr3:56590930-56591239	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPD	chr3:56590969-56591448	K562	blood:	n/a	n/a
21	CEBPD	chr3:56590912-56591401	HepG2	liver:	n/a	n/a
22	CHD1	chr3:56590763-56591987	H1-hESC	embryonic stem cell:	n/a	n/a
23	CHD1	chr3:56590604-56590631	GM12878	blood:	n/a	n/a
24	CHD1	chr3:56590974-56592404	GM12878	blood:	n/a	n/a
25	CHD2	chr3:56590702-56592462	GM12878	blood:	n/a	n/a
26	CHD2	chr3:56590971-56591918	K562	blood:	n/a	n/a
27	CHD2	chr3:56590847-56591845	Hela-S3	cervix:	n/a	n/a
28	CHD2	chr3:56590973-56591313	HepG2	liver:	n/a	n/a
29	CHD2	chr3:56590961-56591393	H1-hESC	embryonic stem cell:	n/a	n/a
30	CREB1	chr3:56590847-56591444	H1-hESC	embryonic stem cell:	n/a	n/a
31	CREB1	chr3:56590865-56591792	HepG2	liver:	n/a	n/a
32	CREB1	chr3:56590863-56591433	H1-hESC	embryonic stem cell:	n/a	n/a
33	CREB1	chr3:56590903-56591431	A549	lung:	n/a	n/a
34	CTCF	chr3:56591680-56591830	RPTEC	kidney:	n/a	n/a
35	CTCF	chr3:56591680-56591830	AoAF	blood vessel:	n/a	n/a
36	CTCF	chr3:56591657-56591822	SK-N-SH_RA	brain:	n/a	n/a
37	CTCF	chr3:56591687-56591812	H1-hESC	embryonic stem cell:	n/a	n/a
38	CTCF	chr3:56591584-56591851	GM19240	blood:	n/a	n/a
39	CTCF	chr3:56591660-56591810	GM12872	blood:	n/a	n/a
40	CTCF	chr3:56591680-56591830	GM12872	blood:	n/a	n/a
41	CTCF	chr3:56591229-56591390	GM12892	blood:	n/a	n/a
42	CTCF	chr3:56591660-56591810	NHEK	skin:	n/a	n/a
43	CTCF	chr3:56591700-56591850	GM12867	blood:	n/a	n/a
44	CTCF	chr3:56591700-56591850	HRPEpiC	eye:	n/a	n/a
45	CTCF	chr3:56591340-56591490	HRPEpiC	eye:	n/a	n/a
46	CTCF	chr3:56591160-56591310	GM12869	blood:	n/a	n/a
47	CTCF	chr3:56591720-56591870	HA-sp	spinal cord:	n/a	n/a
48	CTCF	chr3:56591407-56592324	A549	lung:	n/a	n/a
49	CTCF	chr3:56591240-56591390	SAEC	small airway:	n/a	n/a
50	CTCF	chr3:56591671-56591877	A549	lung:	n/a	n/a

(count:549 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:56591125-56591175	HMEC	breast:	n/a
2	chr3:56591717-56591767	HUVEC	blood vessel:	n/a
3	chr3:56591097-56591147	BJ	skin:	n/a
4	chr3:56591125-56591175	AG04450	lung:	fetal
5	chr3:56591717-56591767	HepG2	liver:	n/a
6	chr3:56591125-56591175	ECC-1	luminal epithelium:	n/a
7	chr3:56590940-56590990	RPTEC	kidney:	n/a
8	chr3:56590940-56590990	HNPCEpiC	eye:	n/a
9	chr3:56591097-56591147	NHBE	bronchial:	n/a
10	chr3:56591241-56591291	ovcar-3	ovarian:	n/a
11	chr3:56591241-56591291	SK-N-SH	brain:	n/a
12	chr3:56590942-56590992	HAEpiC	amniotic membrane:	n/a
13	chr3:56590734-56590784	U87	brain:	n/a
14	chr3:56590734-56590784	HEEpiC	esophagus:	n/a
15	chr3:56590734-56590784	SKMC	muscle:	n/a
16	chr3:56590734-56590784	BE2_C	brain:	n/a
17	chr3:56591097-56591147	SAEC	small airway:	n/a
18	chr3:56590734-56590784	HCT-116	colon:	n/a
19	chr3:56591125-56591175	GM12892	blood:	n/a
20	chr3:56590942-56590992	HRPEpiC	eye:	n/a
21	chr3:56590734-56590784	AG04450	lung:	fetal
22	chr3:56591717-56591767	GM19239	blood:	n/a
23	chr3:56590942-56590992	ProgFib	skin:	n/a
24	chr3:56591241-56591291	NHBE	bronchial:	n/a
25	chr3:56590940-56590990	NT2-D1	testis:	n/a
26	chr3:56591097-56591147	AG04450	lung:	fetal
27	chr3:56591125-56591175	K562	blood:	n/a
28	chr3:56590734-56590784	NT2-D1	testis:	n/a
29	chr3:56590940-56590990	HUVEC	blood vessel:	n/a
30	chr3:56590734-56590784	AoSMC	blood vessel:	n/a
31	chr3:56591045-56591095	GM06990	blood:	n/a
32	chr3:56591717-56591767	PANC-1	pancreas:	n/a
33	chr3:56591097-56591147	ECC-1	luminal epithelium:	n/a
34	chr3:56591190-56591240	GM06990	blood:	n/a
35	chr3:56590942-56590992	LNCaP	prostate:	n/a
36	chr3:56590940-56590990	HRPEpiC	eye:	n/a
37	chr3:56590940-56590990	SAEC	small airway:	n/a
38	chr3:56590734-56590784	HCPEpiC	choroid plexus:	n/a
39	chr3:56591045-56591095	HRE	kidney:	n/a
40	chr3:56590942-56590992	SK-N-SH	brain:	n/a
41	chr3:56591045-56591095	Hela-S3	cervix:	n/a
42	chr3:56591045-56591095	H1-hESC	embryonic stem cell:	embryo
43	chr3:56590940-56590990	Jurkat	blood:	n/a
44	chr3:56590940-56590990	PFSK-1	brain:	n/a
45	chr3:56591045-56591095	AG10803	skin:	n/a
46	chr3:56590942-56590992	AG04449	skin:	fetal
47	chr3:56590940-56590990	PrEC	prostate:	n/a
48	chr3:56591190-56591240	NHDF-neo	bronchial:	n/a
49	chr3:56591045-56591095	GM12891	blood:	n/a
50	chr3:56590942-56590992	Jurkat	blood:	n/a

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:56588153..56590621-chr3:56591371..56592977,2	K562	blood:
2	chr17:61042877..61045351-chr3:56589650..56591304,2	MCF-7	breast:
3	chr3:56591141..56591731-chr7:66766903..66767777,2	Hela-S3	cervix:
4	chr3:56588808..56592620-chr3:56662133..56663692,3	K562	blood:
5	chr3:56589716..56592620-chr3:56662133..56663652,2	K562	blood:
6	chr3:56590666..56591170-chr6:28953586..28954086,2	HCT-116	colon:
7	chr3:56589231..56591997-chr3:56715959..56718849,3	K562	blood:
8	chr11:122932229..122934551-chr3:56588931..56590451,2	K562	blood:
9	chr11:85375746..85376542-chr3:56590683..56591527,2	Hela-S3	cervix:
10	chr3:56589586..56592975-chr3:56714350..56719200,6	K562	blood:

No data

Variant related genes	Relation type
CCDC66	TF binding region
CCDC66	CpG island
ENSG00000180376	chromatin interactions
ENSG00000106610	chromatin interactions
ENSG00000109971	chromatin interactions
ENSG00000137504	chromatin interactions
ENSG00000067601	chromatin interactions
ENSG00000263931	chromatin interactions
ENSG00000163946	chromatin interactions
ENSG00000227214	chromatin interactions

Extended variants
information (count: 110 )
Associated
traits (count: 79 )

Variant overlapped rSNPs/rCNVs (count:110 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9834064	chr3:56590069-56590070	Enhancers Active TSS	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs537813916	chr3:56590129-56590130	Enhancers Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
3	rs568951995	chr3:56590155-56590156	Enhancers Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
4	rs537815515	chr3:56590161-56590162	Enhancers Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
5	rs557791877	chr3:56590163-56590164	Enhancers Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
6	rs556527454	chr3:56590203-56590204	Active TSS Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
7	rs76873611	chr3:56590300-56590301	Active TSS Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
8	rs555642960	chr3:56590311-56590312	Active TSS Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
9	rs534126408	chr3:56590323-56590324	Active TSS Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
10	rs115289613	chr3:56590338-56590339	Active TSS Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
11	rs181555328	chr3:56590348-56590349	Active TSS Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
12	rs370998479	chr3:56590454-56590455	Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs536195392	chr3:56590455-56590456	Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs141433378	chr3:56590482-56590483	Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs186587685	chr3:56590502-56590503	Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs542209866	chr3:56590549-56590550	Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs11333046	chr3:56590566-56590567	Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs145089274	chr3:56590588-56590589	Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs575695077	chr3:56590609-56590610	Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs554391760	chr3:56590644-56590645	Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs544158318	chr3:56590650-56590651	Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs564182082	chr3:56590652-56590653	Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs191047350	chr3:56590690-56590691	Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
24	rs182223128	chr3:56590755-56590756	Active TSS Enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
25	rs374366061	chr3:56590770-56590771	Active TSS Enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
26	rs145668693	chr3:56590773-56590774	Active TSS Enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
27	rs529435207	chr3:56590775-56590776	Active TSS Enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
28	rs370967674	chr3:56590781-56590782	Active TSS Enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
29	rs71072166	chr3:56590788-56590789	Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
30	rs58160140	chr3:56590794-56590795	Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
31	rs541148575	chr3:56590796-56590797	Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
32	rs201137397	chr3:56590808-56590809	Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
33	rs186013403	chr3:56590813-56590814	Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
34	rs72877266	chr3:56590826-56590827	Active TSS	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs190952033	chr3:56590834-56590835	Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
36	rs371631038	chr3:56590846-56590847	Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
37	rs183145689	chr3:56590847-56590848	Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
38	rs147810859	chr3:56590869-56590870	Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
39	rs369418283	chr3:56590871-56590872	Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
40	rs112724868	chr3:56590872-56590873	Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
41	rs186974431	chr3:56590909-56590910	Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
42	rs72877267	chr3:56590921-56590922	Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
43	rs112966280	chr3:56590925-56590926	Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
44	rs111875677	chr3:56590933-56590934	Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
45	rs576090495	chr3:56590966-56590967	Active TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
46	rs553748704	chr3:56590969-56590970	Active TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
47	rs573901512	chr3:56590970-56590971	Active TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
48	rs543047365	chr3:56590981-56590982	Active TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
49	rs536011517	chr3:56590998-56590999	Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
50	rs138950054	chr3:56591025-56591026	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:79)

Disease	PMID	Source
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Hirschsprung''s Disease	21712996	CNVD
Acute myeloid leukemia	20729466	CNVD
Glioblastoma multiforme	21080181	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
T-cell prolymphocytic leukemia	17713554	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	18438408	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Esophageal cancer	20955586	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17133270	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Acute myeloid leukemia	21251322	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
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Breast cancer	21785460	CNVD
Neuroblastoma	17327916	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16608533	CNVD
Prostate cancer	21965145	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Renal cell carcinoma	18765545	CNVD
small cell lung cancer	20016488	CNVD
Prostate cancer	18632612	CNVD
Cancer	20164919	CNVD
Myelofibrosis	22110671	CNVD
Urothelial cell carcinoma	18451213	CNVD
Breast cancer	19490591	CNVD
Autism	18414403	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-small cell lung cancer	20864512	CNVD
Metastatic melanoma	17975146	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:204 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:56590000-56590400	Enhancers	HepG2	liver
2	chr3:56590000-56592000	Active TSS	NHDF-Ad	bronchial
3	chr3:56590200-56590400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
4	chr3:56590200-56590400	Enhancers	Primary T regulatory cells fromperipheralblood	blood
5	chr3:56590200-56590400	Bivalent/Poised TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr3:56590200-56590400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
7	chr3:56590200-56590400	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr3:56590200-56590400	Enhancers	Dnd41	blood
9	chr3:56590200-56590600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
10	chr3:56590200-56590600	Enhancers	Primary T killer memory cells from peripheral blood	blood
11	chr3:56590200-56591800	Active TSS	iPS-18 Cell Line	embryonic stem cell
12	chr3:56590200-56592000	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr3:56590200-56592000	Active TSS	Duodenum Mucosa	Duodenum
14	chr3:56590200-56592000	Active TSS	Fetal Heart	heart
15	chr3:56590200-56592000	Active TSS	Fetal Kidney	kidney
16	chr3:56590200-56592600	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
17	chr3:56590200-56592600	Active TSS	HUES64 Cell Line	embryonic stem cell
18	chr3:56590200-56592600	Active TSS	Duodenum Smooth Muscle	Duodenum
19	chr3:56590200-56592600	Active TSS	Pancreatic Islets	Pancreatic Islet
20	chr3:56590400-56590600	Flanking Active TSS	Primary B cells from cord blood	blood
21	chr3:56590400-56590600	Enhancers	Primary B cells from peripheral blood	blood
22	chr3:56590400-56590600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
23	chr3:56590400-56590600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr3:56590400-56590600	Flanking Active TSS	Muscle Satellite Cultured Cells	--
25	chr3:56590400-56590600	Flanking Active TSS	Brain Germinal Matrix	brain
26	chr3:56590400-56590600	Bivalent/Poised TSS	Fetal Brain Female	brain
27	chr3:56590400-56590600	Flanking Active TSS	Dnd41	blood
28	chr3:56590400-56590600	Flanking Bivalent TSS/Enh	HUVEC	blood vessel
29	chr3:56590400-56590800	Enhancers	Primary neutrophils fromperipheralblood	blood
30	chr3:56590400-56590800	Flanking Active TSS	Primary T cells from cord blood	blood
31	chr3:56590400-56590800	Flanking Active TSS	Primary T cells fromperipheralblood	blood
32	chr3:56590400-56590800	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
33	chr3:56590400-56590800	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
34	chr3:56590400-56590800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr3:56590400-56590800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
36	chr3:56590400-56591200	Active TSS	Primary hematopoietic stem cells	blood
37	chr3:56590400-56591200	Active TSS	HepG2	liver
38	chr3:56590400-56591400	Active TSS	Primary hematopoietic stem cells short term culture	blood
39	chr3:56590400-56591400	Active TSS	Primary T helper cells fromperipheralblood	blood
40	chr3:56590400-56591400	Active TSS	Adipose Nuclei	Adipose
41	chr3:56590400-56591800	Active TSS	Primary monocytes fromperipheralblood	blood
42	chr3:56590400-56591800	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
43	chr3:56590400-56591800	Active TSS	Cortex derived primary cultured neurospheres	brain
44	chr3:56590400-56591800	Active TSS	Liver	Liver
45	chr3:56590400-56591800	Active TSS	Brain Substantia Nigra	brain
46	chr3:56590400-56591800	Active TSS	Colon Smooth Muscle	Colon
47	chr3:56590400-56591800	Active TSS	Fetal Brain Male	brain
48	chr3:56590400-56591800	Active TSS	Fetal Lung	lung
49	chr3:56590400-56591800	Active TSS	Rectal Mucosa Donor 29	rectum
50	chr3:56590400-56591800	Active TSS	Rectal Smooth Muscle	rectum

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