Variant report

Variant	nsv427915
Chromosome Location	chr12:75047293-75172692
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	CEBPB	chr12:75156716-75156999	HepG2	liver:	n/a	chr12:75156857-75156870 chr12:75156859-75156868 chr12:75156857-75156868 chr12:75156859-75156868 chr12:75156859-75156868 chr12:75156858-75156869 chr12:75156859-75156868 chr12:75156857-75156870 chr12:75156857-75156870
2	CEBPB	chr12:75118644-75118950	HepG2	liver:	n/a	chr12:75118784-75118793 chr12:75118784-75118793 chr12:75118784-75118793 chr12:75118701-75118712 chr12:75118782-75118795
3	CEBPB	chr12:75060605-75060800	A549	lung:	n/a	n/a
4	CEBPB	chr12:75118652-75118932	A549	lung:	n/a	chr12:75118784-75118793 chr12:75118784-75118793 chr12:75118784-75118793 chr12:75118701-75118712 chr12:75118782-75118795
5	CEBPB	chr12:75118639-75119188	ECC-1	luminal epithelium:	n/a	chr12:75118784-75118793 chr12:75118784-75118793 chr12:75118784-75118793 chr12:75118701-75118712 chr12:75118782-75118795
6	CEBPB	chr12:75118635-75118948	IMR90	lung:	n/a	chr12:75118784-75118793 chr12:75118784-75118793 chr12:75118784-75118793 chr12:75118701-75118712 chr12:75118782-75118795
7	CEBPB	chr12:75087412-75087644	HepG2	liver:	n/a	chr12:75087454-75087465
8	CEBPB	chr12:75091403-75091631	A549	lung:	n/a	chr12:75091554-75091565 chr12:75091554-75091567 chr12:75091554-75091567
9	CEBPB	chr12:75156761-75157040	IMR90	lung:	n/a	chr12:75156857-75156870 chr12:75156859-75156868 chr12:75156857-75156868 chr12:75156859-75156868 chr12:75156859-75156868 chr12:75156858-75156869 chr12:75156859-75156868 chr12:75156857-75156870 chr12:75156857-75156870
10	CEBPB	chr12:75051853-75051951	IMR90	lung:	n/a	n/a
11	CEBPB	chr12:75118638-75118882	H1-hESC	embryonic stem cell:	n/a	chr12:75118784-75118793 chr12:75118784-75118793 chr12:75118784-75118793 chr12:75118701-75118712 chr12:75118782-75118795
12	CEBPB	chr12:75126094-75126486	HCT-116	colon:	n/a	n/a
13	CEBPB	chr12:75150795-75150866	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr12:75156758-75156986	A549	lung:	n/a	chr12:75156857-75156870 chr12:75156859-75156868 chr12:75156857-75156868 chr12:75156859-75156868 chr12:75156859-75156868 chr12:75156858-75156869 chr12:75156859-75156868 chr12:75156857-75156870 chr12:75156857-75156870
15	CEBPB	chr12:75063766-75064042	HepG2	liver:	n/a	chr12:75063872-75063883
16	CEBPB	chr12:75126041-75126359	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr12:75168732-75168947	A549	lung:	n/a	n/a
18	CEBPB	chr12:75171901-75172235	MCF-7	breast:	n/a	n/a
19	CEBPZ	chr12:75056377-75056383	HepG2	liver:	n/a	n/a
20	CTCF	chr12:75071405-75071442	GM20000	blood:	n/a	n/a
21	CTCF	chr12:75141180-75141330	Hela-S3	cervix:	n/a	chr12:75141267-75141285 chr12:75141268-75141284
22	CTCF	chr12:75141173-75141371	HUVEC	blood vessel:	n/a	chr12:75141267-75141285 chr12:75141268-75141284
23	CTCF	chr12:75082857-75083173	HepG2	liver:	n/a	chr12:75083027-75083045 chr12:75083032-75083040 chr12:75083029-75083050
24	CTCF	chr12:75082888-75083154	Medullo	brain:	n/a	chr12:75083027-75083045 chr12:75083032-75083040 chr12:75083029-75083050
25	CTCF	chr12:75082900-75083050	RPTEC	kidney:	n/a	chr12:75083027-75083045 chr12:75083032-75083040 chr12:75083029-75083050
26	CTCF	chr12:75141200-75141350	HRPEpiC	eye:	n/a	chr12:75141267-75141285 chr12:75141268-75141284
27	CTCF	chr12:75141200-75141350	MCF-7	breast:	n/a	chr12:75141267-75141285 chr12:75141268-75141284
28	CTCF	chr12:75141200-75141350	RPTEC	kidney:	n/a	chr12:75141267-75141285 chr12:75141268-75141284
29	CTCF	chr12:75141180-75141330	HCPEpiC	choroid plexus:	n/a	chr12:75141267-75141285 chr12:75141268-75141284
30	CTCF	chr12:75083020-75083170	GM12873	blood:	n/a	chr12:75083027-75083045 chr12:75083032-75083040 chr12:75083029-75083050
31	CTCF	chr12:75082940-75083090	GM12868	blood:	n/a	chr12:75083027-75083045 chr12:75083032-75083040 chr12:75083029-75083050
32	CTCF	chr12:75082940-75083090	HFF-Myc	foreskin:	n/a	chr12:75083027-75083045 chr12:75083032-75083040 chr12:75083029-75083050
33	CTCF	chr12:75082960-75083110	HCPEpiC	choroid plexus:	n/a	chr12:75083027-75083045 chr12:75083032-75083040 chr12:75083029-75083050
34	CTCF	chr12:75082940-75083090	HMEC	breast:	n/a	chr12:75083027-75083045 chr12:75083032-75083040 chr12:75083029-75083050
35	CTCF	chr12:75082940-75083090	Hela-S3	cervix:	n/a	chr12:75083027-75083045 chr12:75083032-75083040 chr12:75083029-75083050
36	CTCF	chr12:75082920-75083070	HUVEC	blood vessel:	n/a	chr12:75083027-75083045 chr12:75083032-75083040 chr12:75083029-75083050
37	CTCF	chr12:75083020-75083170	GM12874	blood:	n/a	chr12:75083027-75083045 chr12:75083032-75083040 chr12:75083029-75083050
38	CTCF	chr12:75082935-75083108	GM13976	blood:	n/a	chr12:75083027-75083045 chr12:75083032-75083040 chr12:75083029-75083050
39	CTCF	chr12:75082960-75083110	HRPEpiC	eye:	n/a	chr12:75083027-75083045 chr12:75083032-75083040 chr12:75083029-75083050
40	CTCF	chr12:75141132-75141517	MCF-7	breast:	n/a	chr12:75141267-75141285 chr12:75141268-75141284
41	CTCF	chr12:75082900-75083050	HA-sp	spinal cord:	n/a	chr12:75083027-75083045 chr12:75083032-75083040 chr12:75083029-75083050
42	CTCF	chr12:75082821-75083209	K562	blood:	n/a	chr12:75083027-75083045 chr12:75083032-75083040 chr12:75083029-75083050
43	CTCF	chr12:75083060-75083210	A549	lung:	n/a	n/a
44	CTCF	chr12:75082920-75083070	GM12872	blood:	n/a	chr12:75083027-75083045 chr12:75083032-75083040 chr12:75083029-75083050
45	CTCF	chr12:75082960-75083110	HVMF	connective:	n/a	chr12:75083027-75083045 chr12:75083032-75083040 chr12:75083029-75083050
46	CTCF	chr12:75083011-75083035	MCF-7	breast:	n/a	n/a
47	CTCF	chr12:75082901-75083137	K562	blood:	n/a	chr12:75083027-75083045 chr12:75083032-75083040 chr12:75083029-75083050
48	CTCF	chr12:75141200-75141336	Spleen_OC	spleen:	n/a	chr12:75141267-75141285 chr12:75141268-75141284
49	CTCF	chr12:75082768-75083268	MCF-7	breast:	n/a	chr12:75083027-75083045 chr12:75083032-75083040 chr12:75083029-75083050
50	CTCF	chr12:75082900-75083050	NHEK	skin:	n/a	chr12:75083027-75083045 chr12:75083032-75083040 chr12:75083029-75083050

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:75057913-75057963	A549	lung:	n/a
2	chr12:75057893-75057943	NH-A	brain:	n/a
3	chr12:75057913-75057963	HCF	heart:	n/a
4	chr12:75057913-75057963	T-47D	breast:	n/a
5	chr12:75057913-75057963	Caco-2	colon:	n/a
6	chr12:75116380-75116430	AoSMC	blood vessel:	n/a
7	chr12:75116380-75116430	HCM	heart:	n/a
8	chr12:75116380-75116430	HRE	kidney:	n/a
9	chr12:75057913-75057963	Hela-S3	cervix:	n/a
10	chr12:75057913-75057963	HRCEpiC	kidney:	n/a
11	chr12:75057893-75057943	AG04450	lung:	fetal
12	chr12:75057913-75057963	AG09309	skin:	n/a
13	chr12:75057913-75057963	GM12891	blood:	n/a
14	chr12:75057913-75057963	HRPEpiC	eye:	n/a
15	chr12:75116380-75116430	HL-60	blood:	n/a
16	chr12:75057913-75057963	GM12878	blood:	n/a
17	chr12:75116380-75116430	U87	brain:	n/a
18	chr12:75057893-75057943	HCM	heart:	n/a
19	chr12:75057893-75057943	PANC-1	pancreas:	n/a
20	chr12:75116380-75116430	PANC-1	pancreas:	n/a
21	chr12:75057893-75057943	HCPEpiC	choroid plexus:	n/a
22	chr12:75116380-75116430	HCF	heart:	n/a
23	chr12:75057913-75057963	HCPEpiC	choroid plexus:	n/a
24	chr12:75057913-75057963	U87	brain:	n/a
25	chr12:75057913-75057963	AG04449	skin:	fetal
26	chr12:75057893-75057943	HNPCEpiC	eye:	n/a
27	chr12:75057913-75057963	HAEpiC	amniotic membrane:	n/a
28	chr12:75057893-75057943	HIPEpiC	eye:	n/a
29	chr12:75057893-75057943	NT2-D1	testis:	n/a
30	chr12:75057913-75057963	RPTEC	kidney:	n/a
31	chr12:75116380-75116430	HCT-116	colon:	n/a
32	chr12:75057893-75057943	NB4	blood:	n/a
33	chr12:75057913-75057963	AoSMC	blood vessel:	n/a
34	chr12:75057913-75057963	HRE	kidney:	n/a
35	chr12:75057913-75057963	SKMC	muscle:	n/a
36	chr12:75057893-75057943	HMEC	breast:	n/a
37	chr12:75057893-75057943	NHBE	bronchial:	n/a
38	chr12:75116380-75116430	MCF10A-Er-Src	breast:	n/a
39	chr12:75057913-75057963	AG04450	lung:	fetal
40	chr12:75057913-75057963	HEK293	kidney:	embryo
41	chr12:75057893-75057943	CMK	blood:	n/a
42	chr12:75057893-75057943	GM12878	blood:	n/a
43	chr12:75057913-75057963	SK-N-SH	brain:	n/a
44	chr12:75057913-75057963	SK-N-SH_RA	brain:	n/a
45	chr12:75116380-75116430	NHDF-neo	bronchial:	n/a
46	chr12:75057893-75057943	HEEpiC	esophagus:	n/a
47	chr12:75057913-75057963	BE2_C	brain:	n/a
48	chr12:75057893-75057943	HPAEpiC	pulmonary alveolar:	n/a
49	chr12:75116380-75116430	GM12878	blood:	n/a
50	chr12:75057913-75057963	HL-60	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr12:75143585..75146196-chr12:75682282..75684719,2	MCF-7	breast:
2	chr12:75082770..75083374-chr12:75481266..75482191,2	MCF-7	breast:
3	chr12:75082733..75083422-chr12:75196794..75197408,2	MCF-7	breast:
4	chr12:75106983..75109185-chr12:75115008..75117745,2	K562	blood:
5	chr12:75087580..75089343-chr12:75091568..75094109,2	MCF-7	breast:
6	chr12:75140866..75141740-chr12:75683619..75684268,4	MCF-7	breast:
7	chr12:75082582..75083563-chr12:75481520..75482214,2	MCF-7	breast:
8	chr12:75088132..75090058-chr12:75866248..75868411,2	K562	blood:
9	chr12:75082796..75083489-chr12:75451709..75452443,2	MCF-7	breast:
10	chr12:75123651..75124270-chr3:64290669..64291523,2	MCF-7	breast:
11	chr12:75106983..75109185-chr12:75115008..75117745,2	K562	blood:
12	chr12:74931373..74934203-chr12:75080522..75082837,2	MCF-7	breast:
13	chr12:75082779..75083551-chr12:75899376..75900114,2	MCF-7	breast:
14	chr12:75102624..75104674-chr12:75106100..75107854,2	MCF-7	breast:
15	chr12:75082737..75083566-chr12:75727830..75728655,2	MCF-7	breast:
16	chr12:75140910..75141773-chr12:75451603..75452321,3	MCF-7	breast:
17	chr12:75120647..75123375-chr12:75123565..75125151,2	MCF-7	breast:
18	chr12:75160845..75163008-chr12:75163683..75165464,2	MCF-7	breast:
19	chr12:75160845..75163008-chr12:75163683..75165464,2	MCF-7	breast:
20	chr12:75087580..75089343-chr12:75091568..75094109,2	MCF-7	breast:
21	chr12:75102624..75104674-chr12:75106100..75107854,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KCNC2-7	chr12:75121818-75122631	NONHSAT029512
2	lnc-ATXN7L3B-4	chr12:75050341-75050640	NONHSAT029511

Variant related genes	Relation type
ENSG00000188646	TF binding region
ENSG00000257998	TF binding region
ENSG00000257323	TF binding region
ENSG00000188646	CpG island
ENSG00000257998	CpG island
ENSG00000257323	CpG island
ENSG00000253719	chromatin interactions
ENSG00000173401	chromatin interactions
ENSG00000257386	chromatin interactions
ENSG00000257998	chromatin interactions

Extended variants
information (count: 1619 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:1619 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs192101009	chr12:75050355-75050356	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
2	rs530059151	chr12:75050429-75050430	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
3	rs540200228	chr12:75050469-75050470	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
4	rs560092766	chr12:75050533-75050534	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
5	rs532739890	chr12:75050560-75050561	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
6	rs76147704	chr12:75050615-75050616	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
7	rs552731081	chr12:75050616-75050617	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
8	rs147789716	chr12:75050623-75050624	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
9	rs550961200	chr12:75050637-75050638	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
10	rs143690906	chr12:75056200-75056201	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs553609762	chr12:75056221-75056222	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs554341175	chr12:75056226-75056227	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs532711245	chr12:75056238-75056239	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs551202332	chr12:75056243-75056244	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs571400614	chr12:75056320-75056321	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs68023260	chr12:75056335-75056336	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs78006284	chr12:75056365-75056366	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs74106380	chr12:75056626-75056627	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs572977160	chr12:75056697-75056698	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs147187864	chr12:75056718-75056719	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs558318020	chr12:75056797-75056798	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs556117967	chr12:75056832-75056833	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs575364048	chr12:75056960-75056961	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs377437238	chr12:75056980-75056981	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs11180138	chr12:75056986-75056987	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs560987224	chr12:75057001-75057002	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs530064801	chr12:75057017-75057018	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs545064625	chr12:75057025-75057026	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs77508804	chr12:75057026-75057027	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs201964171	chr12:75057075-75057076	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs200069699	chr12:75057077-75057078	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs369448602	chr12:75057078-75057079	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs140648514	chr12:75057079-75057080	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs200243142	chr12:75057080-75057081	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs12300270	chr12:75057081-75057082	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs563069696	chr12:75057083-75057084	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs187823081	chr12:75057094-75057095	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs550652471	chr12:75057097-75057098	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs373025194	chr12:75057129-75057130	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs55864653	chr12:75057130-75057131	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs56022663	chr12:75057131-75057132	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs71075988	chr12:75057133-75057134	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs200766872	chr12:75057134-75057135	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs201445286	chr12:75057135-75057136	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs375362209	chr12:75057167-75057168	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs11180139	chr12:75057171-75057172	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs60358305	chr12:75057174-75057175	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs7975164	chr12:75057175-75057176	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs375067078	chr12:75057178-75057179	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs570158317	chr12:75057182-75057183	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:72)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Esophageal cancer	21851588	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Ewing''s sarcoma	21437220	CNVD
Testicular germ cell tumor	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
Neurodevelopmental disorder	22521361	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21949216	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21637783	CNVD
Glioblastoma multiforme	21080181	CNVD
Renal cell carcinoma	19461508	CNVD
Burkitt''s lymphoma	18698080	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Lung cancer	18438408	CNVD
Breast cancer	17899364	CNVD
Colorectal cancer	16272173	CNVD
Cancer	16751803	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
small cell lung cancer	20016488	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	21785460	CNVD
Acute myeloid leukemia	21251322	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Burkitt''s lymphoma	20823134	CNVD
abnormal development	18461090	CNVD
Prostate cancer	18632612	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
craniofacial dysmorphism	21918468	CNVD
Breast cancer	17133270	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	22032731	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Urothelial cell carcinoma	18451213	CNVD
Myelofibrosis	22110671	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:45 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:75056200-75056400	Enhancers	Stomach Mucosa	stomach
2	chr12:75056600-75057600	Weak transcription	Stomach Mucosa	stomach
3	chr12:75057600-75058200	Enhancers	Stomach Mucosa	stomach
4	chr12:75061600-75062000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr12:75061600-75062000	Enhancers	NH-A	brain
6	chr12:75064000-75066000	Enhancers	Fetal Brain Male	brain
7	chr12:75079200-75079800	Enhancers	HepG2	liver
8	chr12:75083000-75083400	Enhancers	Brain Anterior Caudate	brain
9	chr12:75084600-75085400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
10	chr12:75091800-75092400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr12:75092400-75095200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr12:75095200-75095400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr12:75106000-75107000	Enhancers	Pancreatic Islets	Pancreatic Islet
14	chr12:75110400-75110800	Enhancers	ES-I3 Cell Line	embryonic stem cell
15	chr12:75110400-75110800	Enhancers	iPS-20b Cell Line	embryonic stem cell
16	chr12:75110800-75111400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr12:75110800-75116600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
18	chr12:75115000-75116800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr12:75115800-75116200	Enhancers	Left Ventricle	heart
20	chr12:75115800-75116400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr12:75116000-75116200	Enhancers	H9 Cell Line	embryonic stem cell
22	chr12:75116000-75116400	Enhancers	ES-I3 Cell Line	embryonic stem cell
23	chr12:75116000-75116400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
24	chr12:75116400-75117000	Enhancers	iPS-18 Cell Line	embryonic stem cell
25	chr12:75116400-75117400	Weak transcription	H9 Cell Line	embryonic stem cell
26	chr12:75116400-75117400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
27	chr12:75116600-75118000	Enhancers	iPS-20b Cell Line	embryonic stem cell
28	chr12:75117400-75117800	Enhancers	H9 Cell Line	embryonic stem cell
29	chr12:75117600-75117800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
30	chr12:75117600-75120000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
31	chr12:75119000-75119400	Enhancers	Muscle Satellite Cultured Cells	--
32	chr12:75126400-75126600	Enhancers	Pancreatic Islets	Pancreatic Islet
33	chr12:75126600-75127000	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
34	chr12:75127000-75127200	Enhancers	Pancreatic Islets	Pancreatic Islet
35	chr12:75127200-75134200	Weak transcription	Pancreatic Islets	Pancreatic Islet
36	chr12:75134200-75134600	Enhancers	Fetal Heart	heart
37	chr12:75134200-75135800	Enhancers	Pancreatic Islets	Pancreatic Islet
38	chr12:75134600-75135000	Weak transcription	Fetal Heart	heart
39	chr12:75135000-75135800	Enhancers	Fetal Heart	heart
40	chr12:75155200-75155400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr12:75155400-75156400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
42	chr12:75156400-75156800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr12:75168600-75168800	Enhancers	A549	lung
44	chr12:75171800-75172000	Enhancers	HSMM	muscle
45	chr12:75171800-75172000	Enhancers	HSMMtube	muscle

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