Variant report

Variant	nsv1012551
Chromosome Location	chr3:84235733-84550197
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:578)
CpG islands
(count:61)
Chromatin interactive
region (count:56)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:578 , 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	chr3:84273367-84273773	K562	blood:	n/a	n/a
2	ARID3A	chr3:84290107-84290897	K562	blood:	n/a	n/a
3	ARID3A	chr3:84289267-84289637	K562	blood:	n/a	n/a
4	ARID3A	chr3:84292970-84293680	K562	blood:	n/a	n/a
5	ARID3A	chr3:84272732-84272814	K562	blood:	n/a	n/a
6	ARID3A	chr3:84297148-84297817	K562	blood:	n/a	n/a
7	ARID3A	chr3:84359301-84359721	K562	blood:	n/a	n/a
8	ARID3A	chr3:84291453-84292437	K562	blood:	n/a	n/a
9	ARID3A	chr3:84355882-84356927	K562	blood:	n/a	n/a
10	ATF1	chr3:84297090-84297296	K562	blood:	n/a	n/a
11	ATF3	chr3:84273532-84273887	K562	blood:	n/a	n/a
12	BCL11A	chr3:84258711-84258860	H1-hESC	embryonic stem cell:	n/a	n/a
13	BCL11A	chr3:84258661-84258935	H1-hESC	embryonic stem cell:	n/a	n/a
14	BHLHE40	chr3:84367720-84367757	K562	blood:	n/a	n/a
15	BHLHE40	chr3:84273675-84273710	K562	blood:	n/a	n/a
16	BHLHE40	chr3:84357564-84358045	K562	blood:	n/a	n/a
17	CCNT2	chr3:84359539-84360032	K562	blood:	n/a	n/a
18	CCNT2	chr3:84295739-84295995	K562	blood:	n/a	n/a
19	CEBPB	chr3:84372480-84372733	K562	blood:	n/a	chr3:84372559-84372572 chr3:84372559-84372572 chr3:84372561-84372572 chr3:84372559-84372570 chr3:84372559-84372572
20	CEBPB	chr3:84372399-84372707	HepG2	liver:	n/a	chr3:84372559-84372572 chr3:84372559-84372572 chr3:84372561-84372572 chr3:84372559-84372570 chr3:84372559-84372572
21	CEBPB	chr3:84420372-84420654	HepG2	liver:	n/a	chr3:84420503-84420514
22	CEBPB	chr3:84401416-84401835	A549	lung:	n/a	chr3:84401594-84401605
23	CEBPB	chr3:84278539-84278757	A549	lung:	n/a	chr3:84278649-84278660 chr3:84278648-84278661
24	CEBPB	chr3:84292933-84293241	K562	blood:	n/a	n/a
25	CEBPB	chr3:84315337-84315578	HepG2	liver:	n/a	chr3:84315468-84315479
26	CEBPB	chr3:84401433-84401795	K562	blood:	n/a	chr3:84401594-84401605
27	CEBPB	chr3:84401430-84401670	H1-hESC	embryonic stem cell:	n/a	chr3:84401594-84401605
28	CEBPB	chr3:84386224-84386245	H1-hESC	embryonic stem cell:	n/a	n/a
29	CEBPB	chr3:84435855-84436087	IMR90	lung:	n/a	chr3:84435985-84435998
30	CEBPB	chr3:84424343-84424540	H1-hESC	embryonic stem cell:	n/a	chr3:84424511-84424522 chr3:84424475-84424486
31	CEBPB	chr3:84424307-84424650	IMR90	lung:	n/a	chr3:84424511-84424522 chr3:84424475-84424486
32	CEBPB	chr3:84424300-84424593	A549	lung:	n/a	chr3:84424511-84424522 chr3:84424475-84424486
33	CEBPB	chr3:84441546-84441860	A549	lung:	n/a	chr3:84441699-84441710 chr3:84441701-84441710 chr3:84441701-84441710
34	CEBPB	chr3:84441522-84441865	IMR90	lung:	n/a	chr3:84441699-84441710 chr3:84441701-84441710 chr3:84441701-84441710
35	CEBPB	chr3:84441548-84441877	HepG2	liver:	n/a	chr3:84441699-84441710 chr3:84441701-84441710 chr3:84441701-84441710
36	CEBPB	chr3:84493061-84493358	HepG2	liver:	n/a	chr3:84493298-84493309 chr3:84493187-84493198
37	CEBPB	chr3:84278527-84278781	HepG2	liver:	n/a	chr3:84278649-84278660 chr3:84278648-84278661
38	CEBPB	chr3:84367531-84367839	K562	blood:	n/a	n/a
39	CEBPB	chr3:84424315-84424664	HepG2	liver:	n/a	chr3:84424511-84424522 chr3:84424475-84424486
40	CEBPB	chr3:84401449-84401838	HepG2	liver:	n/a	chr3:84401594-84401605
41	CEBPB	chr3:84518301-84518506	HepG2	liver:	n/a	chr3:84518398-84518409
42	CEBPB	chr3:84401444-84401867	IMR90	lung:	n/a	chr3:84401594-84401605
43	CEBPB	chr3:84424332-84424656	K562	blood:	n/a	chr3:84424511-84424522 chr3:84424475-84424486
44	CEBPD	chr3:84273397-84273745	K562	blood:	n/a	n/a
45	CHD2	chr3:84367313-84367694	K562	blood:	n/a	n/a
46	CHD2	chr3:84365215-84367038	K562	blood:	n/a	n/a
47	CTCF	chr3:84516160-84516235	GM13976	blood:	n/a	n/a
48	CTCF	chr3:84367751-84367810	MCF-7	breast:	n/a	n/a
49	CTCF	chr3:84266620-84266770	GM06990	blood:	n/a	n/a
50	CTCF	chr3:84440123-84440219	Fibrobl	skin:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:84259272-84259322	NHDF-neo	bronchial:	n/a
2	chr3:84259272-84259322	AG10803	skin:	n/a
3	chr3:84259272-84259322	GM06990	blood:	n/a
4	chr3:84259272-84259322	GM19239	blood:	n/a
5	chr3:84259272-84259322	HEEpiC	esophagus:	n/a
6	chr3:84259272-84259322	GM12891	blood:	n/a
7	chr3:84259272-84259322	U87	brain:	n/a
8	chr3:84259272-84259322	HNPCEpiC	eye:	n/a
9	chr3:84259272-84259322	PFSK-1	brain:	n/a
10	chr3:84259272-84259322	HL-60	blood:	n/a
11	chr3:84259272-84259322	PANC-1	pancreas:	n/a
12	chr3:84259272-84259322	AG09309	skin:	n/a
13	chr3:84259272-84259322	A549	lung:	n/a
14	chr3:84259272-84259322	NH-A	brain:	n/a
15	chr3:84259272-84259322	BJ	skin:	n/a
16	chr3:84259272-84259322	NT2-D1	testis:	n/a
17	chr3:84259272-84259322	ProgFib	skin:	n/a
18	chr3:84259272-84259322	SK-N-MC	brain:	n/a
19	chr3:84259272-84259322	GM12878	blood:	n/a
20	chr3:84259272-84259322	HIPEpiC	eye:	n/a
21	chr3:84259272-84259322	HUVEC	blood vessel:	n/a
22	chr3:84259272-84259322	SK-N-SH_RA	brain:	n/a
23	chr3:84259272-84259322	Hela-S3	cervix:	n/a
24	chr3:84259272-84259322	AG04449	skin:	fetal
25	chr3:84259272-84259322	HCT-116	colon:	n/a
26	chr3:84259272-84259322	HRPEpiC	eye:	n/a
27	chr3:84259272-84259322	GM12892	blood:	n/a
28	chr3:84259272-84259322	PrEC	prostate:	n/a
29	chr3:84259272-84259322	AG09319	gingival:	n/a
30	chr3:84259272-84259322	HAEpiC	amniotic membrane:	n/a
31	chr3:84259272-84259322	NHBE	bronchial:	n/a
32	chr3:84259272-84259322	RPTEC	kidney:	n/a
33	chr3:84259272-84259322	AG04450	lung:	fetal
34	chr3:84259272-84259322	NB4	blood:	n/a
35	chr3:84259272-84259322	CMK	blood:	n/a
36	chr3:84259272-84259322	HCPEpiC	choroid plexus:	n/a
37	chr3:84259272-84259322	HCF	heart:	n/a
38	chr3:84259272-84259322	HPAEpiC	pulmonary alveolar:	n/a
39	chr3:84259272-84259322	MCF-7	breast:	n/a
40	chr3:84259272-84259322	HRCEpiC	kidney:	n/a
41	chr3:84259272-84259322	HepG2	liver:	n/a
42	chr3:84259272-84259322	BE2_C	brain:	n/a
43	chr3:84259272-84259322	T-47D	breast:	n/a
44	chr3:84259272-84259322	AoSMC	blood vessel:	n/a
45	chr3:84259272-84259322	H1-hESC	embryonic stem cell:	embryo
46	chr3:84259272-84259322	ECC-1	luminal epithelium:	n/a
47	chr3:84259272-84259322	LNCaP	prostate:	n/a
48	chr3:84259272-84259322	Caco-2	colon:	n/a
49	chr3:84259272-84259322	HRE	kidney:	n/a
50	chr3:84259272-84259322	HCM	heart:	n/a

(count:56 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr3:84356909..84360562-chr3:84364606..84368872,4	K562	blood:
2	chr3:84273214..84274831-chr3:84277558..84279173,2	K562	blood:
3	chr3:84356909..84360562-chr3:84364606..84368872,4	K562	blood:
4	chr3:84366037..84367790-chr3:84378525..84380184,2	K562	blood:
5	chr3:84312486..84313370-chr3:84322396..84322940,2	K562	blood:
6	chr3:84317854..84319580-chr3:84322579..84324579,2	K562	blood:
7	chr3:84298907..84301682-chr3:84313241..84315136,2	K562	blood:
8	chr3:84292652..84296661-chr3:84352861..84356092,4	K562	blood:
9	chr3:84357730..84359734-chr3:84366154..84368442,2	K562	blood:
10	chr3:84273214..84274831-chr3:84277558..84279173,2	K562	blood:
11	chr3:84294925..84296767-chr3:84321826..84324650,2	K562	blood:
12	chr3:84318285..84321102-chr3:84329948..84332818,2	K562	blood:
13	chr3:84361413..84364247-chr3:84367578..84369122,2	K562	blood:
14	chr3:84294165..84297747-chr3:84356381..84359543,4	K562	blood:
15	chr3:84288330..84291285-chr3:84300301..84302575,2	K562	blood:
16	chr3:84294925..84296767-chr3:84321826..84324650,2	K562	blood:
17	chr3:84105503..84107630-chr3:84297263..84298774,2	K562	blood:
18	chr3:84417663..84419504-chr3:84428051..84430045,2	K562	blood:
19	chr3:84272012..84274831-chr3:84277558..84279788,3	K562	blood:
20	chr3:84494646..84496609-chr3:84500255..84502714,2	K562	blood:
21	chr3:84435082..84438227-chr3:84442146..84444726,3	MCF-7	breast:
22	chr3:84366037..84367790-chr3:84378525..84380184,2	K562	blood:
23	chr3:84179427..84182289-chr3:84355686..84357544,2	K562	blood:
24	chr3:84357730..84359734-chr3:84366154..84368442,2	K562	blood:
25	chr3:84367213..84368807-chr3:84372186..84374961,2	K562	blood:
26	chr3:84353604..84355835-chr3:84358362..84361257,3	K562	blood:
27	chr3:84417663..84419504-chr3:84428051..84430045,2	K562	blood:
28	chr3:84272012..84274831-chr3:84277558..84279788,3	K562	blood:
29	chr3:84367002..84369596-chr3:84374915..84377162,2	K562	blood:
30	chr3:84288330..84291285-chr3:84300301..84302575,2	K562	blood:
31	chr3:84295040..84297747-chr3:84356130..84357881,2	K562	blood:
32	chr3:84294165..84297747-chr3:84356381..84359543,4	K562	blood:
33	chr3:84295040..84297747-chr3:84356130..84357881,2	K562	blood:
34	chr3:84291635..84294526-chr3:84360495..84362082,2	K562	blood:
35	chr3:84287116..84289415-chr3:85550323..85553207,2	K562	blood:
36	chr3:84312486..84313370-chr3:84322396..84322940,2	K562	blood:
37	chr3:84367213..84368807-chr3:84372186..84374961,2	K562	blood:
38	chr3:84295391..84297544-chr3:84358043..84362398,3	K562	blood:
39	chr3:84361413..84364247-chr3:84367578..84369122,2	K562	blood:
40	chr3:84295391..84297544-chr3:84358043..84362398,3	K562	blood:
41	chr3:84494646..84496609-chr3:84500255..84502714,2	K562	blood:
42	chr3:84291635..84294526-chr3:84360495..84362082,2	K562	blood:
43	chr3:84318285..84321102-chr3:84329948..84332818,2	K562	blood:
44	chr3:84291765..84296920-chr3:85550637..85554814,6	K562	blood:
45	chr3:84292652..84295673-chr3:84353499..84356092,3	K562	blood:
46	chr3:84353604..84355835-chr3:84358362..84361257,3	K562	blood:
47	chr3:84256922..84258911-chr3:84259197..84261598,2	MCF-7	breast:
48	chr3:84292652..84296661-chr3:84352861..84356092,4	K562	blood:
49	chr3:84435082..84438227-chr3:84442146..84444726,3	MCF-7	breast:
50	chr3:84292652..84295673-chr3:84353499..84356092,3	K562	blood:

No data

Variant related genes	Relation type
ENSG00000266652	TF binding region
ENSG00000221380	TF binding region
ENSG00000266652	CpG island
ENSG00000221380	CpG island

Extended variants
information (count: 2530 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:2530 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs568108077	chr3:84235735-84235736	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs77173553	chr3:84235775-84235776	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs547460562	chr3:84235825-84235826	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs565953023	chr3:84235871-84235872	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs553369145	chr3:84235897-84235898	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs542842710	chr3:84235949-84235950	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs368035468	chr3:84235970-84235971	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs79788087	chr3:84235977-84235978	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs573432759	chr3:84235993-84235994	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs570205931	chr3:84236005-84236006	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs62254589	chr3:84236006-84236007	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs185325607	chr3:84236015-84236016	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs564974943	chr3:84236072-84236073	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs148840718	chr3:84236101-84236102	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs573348391	chr3:84236105-84236106	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs76003183	chr3:84236111-84236112	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs541968542	chr3:84236149-84236150	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs549963524	chr3:84236150-84236151	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs190092665	chr3:84236154-84236155	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs182740111	chr3:84236169-84236170	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs373024922	chr3:84236191-84236192	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs562184474	chr3:84236201-84236202	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs117416336	chr3:84236203-84236204	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs573966522	chr3:84236210-84236211	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs543689417	chr3:84236271-84236272	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs561771990	chr3:84236284-84236285	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs569858249	chr3:84236306-84236307	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs143508023	chr3:84236307-84236308	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs559378399	chr3:84236315-84236316	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs533574412	chr3:84236321-84236322	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs544348084	chr3:84236332-84236333	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs570221775	chr3:84236368-84236369	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs537372359	chr3:84236381-84236382	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs200332296	chr3:84236413-84236414	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs568080540	chr3:84236422-84236423	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs74570342	chr3:84236427-84236428	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs535400356	chr3:84236441-84236442	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs553909776	chr3:84236454-84236455	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs79882214	chr3:84236464-84236465	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs572094995	chr3:84236482-84236483	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs370943527	chr3:84236513-84236514	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs187427096	chr3:84236518-84236519	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs557704902	chr3:84236530-84236531	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs193184643	chr3:84236588-84236589	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs576161771	chr3:84236614-84236615	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs183800598	chr3:84236639-84236640	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs369688219	chr3:84236661-84236662	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs140688210	chr3:84236706-84236707	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs79641482	chr3:84236747-84236748	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs369757761	chr3:84236765-84236766	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:82)

Disease	PMID	Source
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
Acute myeloid leukemia	20729466	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
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
Acute lymphoblastic leukemia	18458336	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Metanephric adenoma	20802469	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	CNVD
Wilms tumour	21544195	CNVD
Colorectal cancer	16272173	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Soft tissue tumor	16732325	CNVD
Breast cancer	21858162	CNVD
small cell lung cancer	20016488	CNVD
Neurodevelopmental disorder	22521361	CNVD
Medulloblastoma	16783165	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Mental retardation	17124404	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Myelofibrosis	22110671	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
craniofacial dysmorphism	21918468	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Lung squamous cell carcinoma	22363434	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:79 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:84215200-84248000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr3:84236800-84237600	Enhancers	HUES6 Cell Line	embryonic stem cell
3	chr3:84240400-84242200	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
4	chr3:84242200-84243400	Weak transcription	HUES6 Cell Line	embryonic stem cell
5	chr3:84243000-84243800	Enhancers	HUES64 Cell Line	embryonic stem cell
6	chr3:84243200-84243800	Enhancers	HMEC	breast
7	chr3:84243200-84243800	Enhancers	NHEK	skin
8	chr3:84243400-84243600	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
9	chr3:84243400-84243800	Enhancers	iPS-15b Cell Line	embryonic stem cell
10	chr3:84245800-84246600	ZNF genes & repeats	Adipose Nuclei	Adipose
11	chr3:84246000-84246800	ZNF genes & repeats	Pancreas	Pancrea
12	chr3:84256600-84257800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr3:84256600-84259400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr3:84257800-84258800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr3:84258400-84259400	Enhancers	HUES64 Cell Line	embryonic stem cell
16	chr3:84258600-84259000	Enhancers	Cortex derived primary cultured neurospheres	brain
17	chr3:84258600-84259200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
18	chr3:84258600-84259600	Enhancers	ES-I3 Cell Line	embryonic stem cell
19	chr3:84258600-84259600	Enhancers	HUES6 Cell Line	embryonic stem cell
20	chr3:84258800-84259200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr3:84258800-84259200	Enhancers	iPS-20b Cell Line	embryonic stem cell
22	chr3:84258800-84259400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
23	chr3:84258800-84259600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
24	chr3:84258800-84259600	Enhancers	HUES48 Cell Line	embryonic stem cell
25	chr3:84258800-84259600	Enhancers	iPS-18 Cell Line	embryonic stem cell
26	chr3:84268600-84268800	Enhancers	Breast Myoepithelial Primary Cells	Breast
27	chr3:84268800-84269800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
28	chr3:84269800-84270200	Enhancers	Breast Myoepithelial Primary Cells	Breast
29	chr3:84270600-84274400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr3:84273800-84274200	Enhancers	K562	blood
31	chr3:84282600-84283600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr3:84285400-84285800	Active TSS	A549	lung
33	chr3:84287200-84287600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr3:84289400-84297800	Active TSS	K562	blood
35	chr3:84307400-84308000	Enhancers	HUES48 Cell Line	embryonic stem cell
36	chr3:84313000-84313400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr3:84338000-84338800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr3:84341000-84341600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
39	chr3:84350800-84351200	Enhancers	iPS-18 Cell Line	embryonic stem cell
40	chr3:84353000-84360000	Active TSS	K562	blood
41	chr3:84391600-84391800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr3:84396400-84397000	Enhancers	H1 Cell Line	embryonic stem cell
43	chr3:84396800-84397200	Enhancers	HUES6 Cell Line	embryonic stem cell
44	chr3:84396800-84397200	Enhancers	iPS-20b Cell Line	embryonic stem cell
45	chr3:84397000-84397800	Enhancers	iPS-15b Cell Line	embryonic stem cell
46	chr3:84436400-84437400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
47	chr3:84436600-84437000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr3:84484000-84485000	Enhancers	Cortex derived primary cultured neurospheres	brain
49	chr3:84484400-84485000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
50	chr3:84484400-84485200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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