Variant report

Variant	nsv589955
Chromosome Location	chr3:24987823-25113358
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	ATF2	chr3:24993812-24994233	H1-hESC	embryonic stem cell:	n/a	n/a
2	ATF2	chr3:24993855-24994300	H1-hESC	embryonic stem cell:	n/a	n/a
3	BATF	chr3:25049457-25049847	GM12878	blood:	n/a	chr3:25049644-25049654 chr3:25049643-25049654
4	BATF	chr3:25049508-25049846	GM12878	blood:	n/a	chr3:25049644-25049654 chr3:25049643-25049654
5	BRCA1	chr3:25085454-25085513	Hela-S3	cervix:	n/a	n/a
6	BRCA1	chr3:25057869-25057895	GM12878	blood:	n/a	n/a
7	CEBPB	chr3:25063204-25063740	A549	lung:	n/a	n/a
8	CEBPB	chr3:25043924-25044206	H1-hESC	embryonic stem cell:	n/a	chr3:25044068-25044077 chr3:25044068-25044077 chr3:25044068-25044077
9	CEBPB	chr3:25043936-25044191	K562	blood:	n/a	chr3:25044068-25044077 chr3:25044068-25044077 chr3:25044068-25044077
10	CEBPB	chr3:25082301-25082584	HepG2	liver:	n/a	chr3:25082451-25082462
11	CEBPB	chr3:25038559-25038810	HepG2	liver:	n/a	n/a
12	CEBPB	chr3:25024512-25024830	HepG2	liver:	n/a	chr3:25024669-25024680
13	CEBPB	chr3:25063291-25063740	MCF-7	breast:	n/a	n/a
14	CEBPB	chr3:25024582-25024801	Hela-S3	cervix:	n/a	chr3:25024669-25024680
15	CEBPB	chr3:25063283-25063734	MCF-7	breast:	n/a	n/a
16	CEBPB	chr3:25007189-25007775	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr3:25043904-25044225	IMR90	lung:	n/a	chr3:25044068-25044077 chr3:25044068-25044077 chr3:25044068-25044077
18	CEBPB	chr3:25063341-25063696	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr3:25047919-25048119	H1-hESC	embryonic stem cell:	n/a	chr3:25048029-25048040 chr3:25048026-25048043
20	CEBPB	chr3:25007267-25007482	A549	lung:	n/a	n/a
21	CEBPB	chr3:25047884-25048211	IMR90	lung:	n/a	chr3:25048029-25048040 chr3:25048132-25048144 chr3:25048026-25048043
22	CEBPB	chr3:25024507-25024824	IMR90	lung:	n/a	chr3:25024669-25024680
23	CEBPB	chr3:25043902-25044137	A549	lung:	n/a	chr3:25044068-25044077 chr3:25044068-25044077 chr3:25044068-25044077
24	CEBPB	chr3:25063422-25063554	K562	blood:	n/a	n/a
25	CEBPB	chr3:25002367-25002493	HepG2	liver:	n/a	chr3:25002420-25002431 chr3:25002419-25002432
26	CEBPB	chr3:25002724-25002997	HepG2	liver:	n/a	chr3:25002818-25002831 chr3:25002820-25002829 chr3:25002820-25002829 chr3:25002819-25002830 chr3:25002820-25002829 chr3:25002820-25002829 chr3:25002818-25002831 chr3:25002818-25002829
27	CEBPB	chr3:25082439-25082518	H1-hESC	embryonic stem cell:	n/a	chr3:25082451-25082462
28	CEBPB	chr3:25063355-25063683	Hela-S3	cervix:	n/a	n/a
29	CEBPB	chr3:25048670-25048717	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPB	chr3:25032982-25033296	HepG2	liver:	n/a	chr3:25033112-25033123
31	CEBPB	chr3:25100141-25100259	K562	blood:	n/a	chr3:25100221-25100232
32	CEBPB	chr3:25033111-25033197	A549	lung:	n/a	chr3:25033112-25033123
33	CEBPB	chr3:25043943-25044158	HepG2	liver:	n/a	chr3:25044068-25044077 chr3:25044068-25044077 chr3:25044068-25044077
34	CEBPB	chr3:25024625-25024753	H1-hESC	embryonic stem cell:	n/a	chr3:25024669-25024680
35	CEBPB	chr3:25063369-25063663	HepG2	liver:	n/a	n/a
36	CEBPB	chr3:25063424-25063689	A549	lung:	n/a	n/a
37	CEBPB	chr3:25063335-25063656	HCT-116	colon:	n/a	n/a
38	CEBPB	chr3:24992882-24993031	HepG2	liver:	n/a	n/a
39	CEBPB	chr3:25002702-25002970	A549	lung:	n/a	chr3:25002818-25002831 chr3:25002820-25002829 chr3:25002820-25002829 chr3:25002819-25002830 chr3:25002820-25002829 chr3:25002820-25002829 chr3:25002818-25002831 chr3:25002818-25002829
40	CEBPB	chr3:25082375-25082605	A549	lung:	n/a	chr3:25082451-25082462
41	CEBPB	chr3:25047856-25048221	HepG2	liver:	n/a	chr3:25048029-25048040 chr3:25048132-25048144 chr3:25048026-25048043
42	CEBPB	chr3:25047888-25048176	A549	lung:	n/a	chr3:25048029-25048040 chr3:25048132-25048144 chr3:25048026-25048043
43	CEBPB	chr3:25024533-25024818	A549	lung:	n/a	chr3:25024669-25024680
44	CEBPB	chr3:25063337-25063695	A549	lung:	n/a	n/a
45	CEBPB	chr3:25047896-25048169	K562	blood:	n/a	chr3:25048029-25048040 chr3:25048132-25048144 chr3:25048026-25048043
46	CEBPB	chr3:25002688-25002888	K562	blood:	n/a	chr3:25002818-25002831 chr3:25002820-25002829 chr3:25002820-25002829 chr3:25002819-25002830 chr3:25002820-25002829 chr3:25002820-25002829 chr3:25002818-25002831 chr3:25002818-25002829
47	CHD2	chr3:24993862-24994292	H1-hESC	embryonic stem cell:	n/a	n/a
48	CTCF	chr3:25075020-25075170	Caco-2	colon:	n/a	n/a
49	CTCF	chr3:25063427-25063587	SK-N-SH_RA	brain:	n/a	n/a
50	CTCF	chr3:25005380-25005530	NHEK	skin:	n/a	chr3:25005452-25005470

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:25101907-25101957	MCF10A-Er-Src	breast:	n/a
2	chr3:25101907-25101957	HRPEpiC	eye:	n/a
3	chr3:25101907-25101957	MCF-7	breast:	n/a
4	chr3:25101907-25101957	GM19239	blood:	n/a
5	chr3:25101907-25101957	IMR90	lung:	fetal
6	chr3:25101907-25101957	HAEpiC	amniotic membrane:	n/a
7	chr3:25101907-25101957	SAEC	small airway:	n/a
8	chr3:25101907-25101957	BE2_C	brain:	n/a
9	chr3:25101907-25101957	HCM	heart:	n/a
10	chr3:25101907-25101957	HL-60	blood:	n/a
11	chr3:25101907-25101957	NHBE	bronchial:	n/a
12	chr3:25101907-25101957	Hepatocyte	liver:	n/a
13	chr3:25101907-25101957	HEEpiC	esophagus:	n/a
14	chr3:25101907-25101957	NH-A	brain:	n/a
15	chr3:25101907-25101957	H1-hESC	embryonic stem cell:	embryo
16	chr3:25101907-25101957	HMEC	breast:	n/a
17	chr3:25101907-25101957	AG10803	skin:	n/a
18	chr3:25101907-25101957	T-47D	breast:	n/a
19	chr3:25101907-25101957	HCT-116	colon:	n/a
20	chr3:25101907-25101957	HNPCEpiC	eye:	n/a
21	chr3:25101907-25101957	HCPEpiC	choroid plexus:	n/a
22	chr3:25101907-25101957	AoSMC	blood vessel:	n/a
23	chr3:25101907-25101957	ProgFib	skin:	n/a
24	chr3:25101907-25101957	AG04449	skin:	fetal
25	chr3:25101907-25101957	NB4	blood:	n/a
26	chr3:25101907-25101957	ECC-1	luminal epithelium:	n/a
27	chr3:25101907-25101957	RPTEC	kidney:	n/a
28	chr3:25101907-25101957	AG09319	gingival:	n/a
29	chr3:25101907-25101957	HPAEpiC	pulmonary alveolar:	n/a
30	chr3:25101907-25101957	PrEC	prostate:	n/a
31	chr3:25101907-25101957	SK-N-MC	brain:	n/a
32	chr3:25101907-25101957	AG09309	skin:	n/a
33	chr3:25101907-25101957	PFSK-1	brain:	n/a
34	chr3:25101907-25101957	U87	brain:	n/a
35	chr3:25101907-25101957	GM06990	blood:	n/a
36	chr3:25101907-25101957	NHDF-neo	bronchial:	n/a
37	chr3:25101907-25101957	HUVEC	blood vessel:	n/a
38	chr3:25101907-25101957	NT2-D1	testis:	n/a
39	chr3:25101907-25101957	ovcar-3	ovarian:	n/a
40	chr3:25101907-25101957	HRE	kidney:	n/a
41	chr3:25101907-25101957	GM12891	blood:	n/a
42	chr3:25101907-25101957	SKMC	muscle:	n/a
43	chr3:25101907-25101957	GM12878	blood:	n/a
44	chr3:25101907-25101957	LNCaP	prostate:	n/a
45	chr3:25101907-25101957	HRCEpiC	kidney:	n/a
46	chr3:25101907-25101957	HIPEpiC	eye:	n/a
47	chr3:25101907-25101957	HCF	heart:	n/a
48	chr3:25101907-25101957	GM12892	blood:	n/a
49	chr3:25101907-25101957	SK-N-SH	brain:	n/a
50	chr3:25101907-25101957	A549	lung:	n/a

No.	Distal block	Cell Line	Cell type
1	chr3:25063074..25063594-chr3:25635286..25636033,2	MCF-7	breast:
2	chr3:24993898..24995691-chr3:25054784..25056351,2	K562	blood:
3	chr3:24999490..25001286-chr3:25005454..25007613,2	K562	blood:
4	chr3:25005007..25005513-chr3:25136423..25137233,2	MCF-7	breast:
5	chr3:25063013..25063625-chr3:25635402..25636430,4	MCF-7	breast:
6	chr3:25062997..25063972-chr3:25074606..25075214,3	MCF-7	breast:
7	chr3:25062997..25063972-chr3:25074606..25075214,3	MCF-7	breast:
8	chr3:25005071..25005603-chr3:25074628..25075570,3	MCF-7	breast:
9	chr3:24815127..24815890-chr3:25004964..25005522,2	MCF-7	breast:
10	chr3:25039709..25042401-chr3:25047247..25049664,2	K562	blood:
11	chr3:25014243..25016013-chr3:25025962..25028034,2	K562	blood:
12	chr3:25039709..25042401-chr3:25047247..25049664,2	K562	blood:
13	chr1:66682219..66683069-chr3:25078040..25078966,2	HCT-116	colon:
14	chr3:24993898..24995691-chr3:25054784..25056351,2	K562	blood:
15	chr3:25005071..25005603-chr3:25074628..25075570,3	MCF-7	breast:
16	chr3:25012469..25014834-chr3:25636551..25638421,2	MCF-7	breast:
17	chr3:24984996..24987861-chr3:24992367..24994337,2	K562	blood:
18	chr3:25079124..25081667-chr3:25084641..25087586,2	MCF-7	breast:
19	chr3:25109117..25112751-chr3:25632559..25635347,3	K562	blood:
20	chr3:25053220..25055961-chr3:25057808..25059826,2	K562	blood:
21	chr3:24975006..24977097-chr3:24999784..25002405,2	K562	blood:
22	chr3:25079124..25081667-chr3:25084641..25087586,2	MCF-7	breast:
23	chr16:69106267..69106856-chr3:25010489..25010989,2	HCT-116	colon:
24	chr3:25105659..25107199-chr3:25110702..25113407,2	K562	blood:
25	chr3:25032348..25035349-chr3:25037207..25041115,3	MCF-7	breast:
26	chr3:24814926..24815573-chr3:25074600..25075173,3	MCF-7	breast:
27	chr3:24984996..24987861-chr3:24992367..24994337,2	K562	blood:
28	chr3:25105659..25107199-chr3:25110702..25113407,2	K562	blood:
29	chr3:24999490..25001286-chr3:25005454..25007613,2	K562	blood:
30	chr3:25063071..25063645-chr3:25482470..25483148,2	MCF-7	breast:
31	chr3:25053220..25055961-chr3:25057808..25059826,2	K562	blood:
32	chr3:25014243..25016013-chr3:25025962..25028034,2	K562	blood:
33	chr3:25032348..25035349-chr3:25037207..25041115,3	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-THRB-5	chr3:25061654-25061954	NONHSAT088706
2	lnc-RARB-1	chr3:25101616-25101667	ENSG00000237838

Variant related genes	Relation type
RN7SL216P	TF binding region
RNA5SP125	TF binding region
RN7SL216P	CpG island
RNA5SP125	CpG island
ENSG00000229421	chromatin interactions

Extended variants
information (count: 4606 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:4606 , 50 per page) page: 1 2 3 4 5 6 7 ... 93

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs199949805	chr3:24987823-24987824	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs186824207	chr3:24987846-24987847	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs142142043	chr3:24987848-24987849	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs528117581	chr3:24987849-24987850	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs147404399	chr3:24987853-24987854	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs369018028	chr3:24987874-24987875	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs568163495	chr3:24987877-24987878	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs139705697	chr3:24987917-24987918	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs539511196	chr3:24987923-24987924	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs550801302	chr3:24988027-24988028	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs570720514	chr3:24988075-24988076	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs191759658	chr3:24988089-24988090	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs181344540	chr3:24988119-24988120	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs566790515	chr3:24988158-24988159	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs535831929	chr3:24988216-24988217	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs566728828	chr3:24988217-24988218	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs11129172	chr3:24988244-24988245	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs75894178	chr3:24988267-24988268	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs376174077	chr3:24988271-24988272	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs575715297	chr3:24988279-24988280	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs544352509	chr3:24988280-24988281	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs186485007	chr3:24988309-24988310	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs4414811	chr3:24988311-24988312	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs537258555	chr3:24988317-24988318	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs540503700	chr3:24988332-24988333	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs560875823	chr3:24988362-24988363	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs556837220	chr3:24988373-24988374	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs541831350	chr3:24988379-24988380	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs115770077	chr3:24988397-24988398	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs530635157	chr3:24988411-24988412	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs11914730	chr3:24988434-24988435	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs570660151	chr3:24988462-24988463	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs11922530	chr3:24988469-24988470	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs559389858	chr3:24988524-24988525	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs71311517	chr3:24988540-24988541	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs566771986	chr3:24988559-24988560	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs189657611	chr3:24988618-24988619	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs555734964	chr3:24988621-24988622	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs116196872	chr3:24988629-24988630	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs577396550	chr3:24988682-24988683	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs4322969	chr3:24988694-24988695	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs145434121	chr3:24988717-24988718	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs541404502	chr3:24988741-24988742	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs577801521	chr3:24988744-24988745	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs370936797	chr3:24988756-24988757	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs147701513	chr3:24988758-24988759	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs112802050	chr3:24988774-24988775	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs554142616	chr3:24988798-24988799	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs574279915	chr3:24988800-24988801	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs541423710	chr3:24988818-24988819	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:73)

Disease	PMID	Source
Esophageal squamous carcinoma	18405350	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Neuroblastoma	17327916	CNVD
Glioblastoma multiforme	21080181	CNVD
Neuroblastoma	18923191	CNVD
Colorectal cancer	21297112	CNVD
Lynch syndrome	18415027	CNVD
Renal cell carcinoma	18592004	CNVD
Acute myeloid leukemia	20729466	CNVD
Urothelial carcinoma	18382360	CNVD
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Hirschsprung''s Disease	21712996	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
lymphocytic leukemia	21291569	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Intellectual disability	22102821	CNVD
Esophageal cancer	20955586	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	17133270	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Melanoma	20688739	CNVD
Myelofibrosis	22110671	CNVD
Multiple myeloma	17550852	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:403 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:24979200-24998400	Weak transcription	Right Atrium	heart
2	chr3:24987000-24996800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr3:24988800-24989400	Enhancers	Fetal Heart	heart
4	chr3:24990200-24990600	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
5	chr3:24991200-24991400	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
6	chr3:24991400-24991600	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
7	chr3:24992600-24993000	Enhancers	Brain Inferior Temporal Lobe	brain
8	chr3:24992800-24993000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr3:24992800-24993400	Enhancers	Brain Substantia Nigra	brain
10	chr3:24993400-24994200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr3:24993600-24995000	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
12	chr3:24993800-24994400	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
13	chr3:24994000-24994200	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
14	chr3:24994000-24994400	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
15	chr3:24994000-24994400	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
16	chr3:24994000-24994800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
17	chr3:24994000-24994800	Enhancers	Brain Germinal Matrix	brain
18	chr3:24994200-24994400	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
19	chr3:24994200-24994800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr3:24994200-24994800	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
21	chr3:24994400-24994800	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
22	chr3:24994400-24995200	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
23	chr3:24994800-24995000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr3:24994800-24995200	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
25	chr3:24995000-24995200	Enhancers	Fetal Kidney	kidney
26	chr3:24995000-24995600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr3:24995200-24995800	Weak transcription	Fetal Kidney	kidney
28	chr3:24995800-24996000	Enhancers	Fetal Kidney	kidney
29	chr3:24996000-25007800	Weak transcription	Fetal Kidney	kidney
30	chr3:24996200-24997200	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
31	chr3:24996400-24997000	Enhancers	Brain Anterior Caudate	brain
32	chr3:24996800-24997200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr3:24996800-24997400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
34	chr3:24998400-24998600	Enhancers	Right Atrium	heart
35	chr3:24998400-24998800	Enhancers	Adipose Nuclei	Adipose
36	chr3:24998400-24998800	Enhancers	Left Ventricle	heart
37	chr3:24998400-24998800	Enhancers	Lung	lung
38	chr3:24998600-24998800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr3:24998800-25000400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
40	chr3:25000400-25000800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
41	chr3:25000800-25006000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
42	chr3:25004600-25005000	Enhancers	Fetal Heart	heart
43	chr3:25004600-25005600	Enhancers	Fetal Muscle Leg	muscle
44	chr3:25005400-25005800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
45	chr3:25005600-25005800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr3:25005600-25005800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
47	chr3:25005600-25006000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr3:25005600-25006000	Weak transcription	Fetal Muscle Leg	muscle
49	chr3:25005600-25006000	Enhancers	A549	lung
50	chr3:25005600-25006400	Enhancers	Breast Myoepithelial Primary Cells	Breast

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