Variant report

Variant	nsv1049580
Chromosome Location	chr12:86966497-87354132
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	ARID3A	chr12:87328246-87328300	K562	blood:	n/a	n/a
2	ATF1	chr12:87283289-87283337	K562	blood:	n/a	n/a
3	ATF2	chr12:87129495-87130047	GM12878	blood:	n/a	n/a
4	ATF2	chr12:87129390-87130163	GM12878	blood:	n/a	n/a
5	ATF3	chr12:87054371-87054987	A549	lung:	n/a	n/a
6	ATF3	chr12:87054387-87055009	A549	lung:	n/a	n/a
7	ATF3	chr12:87106039-87106609	A549	lung:	n/a	chr12:87106339-87106352
8	ATF3	chr12:87106056-87106583	A549	lung:	n/a	chr12:87106339-87106352
9	ATF3	chr12:87054428-87054989	HCT-116	colon:	n/a	n/a
10	ATF3	chr12:87106001-87106627	HCT-116	colon:	n/a	chr12:87106339-87106352
11	ATF3	chr12:87054426-87055001	HCT-116	colon:	n/a	n/a
12	BACH1	chr12:87077208-87077425	H1-hESC	embryonic stem cell:	n/a	n/a
13	BATF	chr12:87128909-87129147	GM12878	blood:	n/a	chr12:87129029-87129040 chr12:87129124-87129137
14	BATF	chr12:87129616-87130068	GM12878	blood:	n/a	n/a
15	BATF	chr12:87106192-87106389	GM12878	blood:	n/a	chr12:87106276-87106287 chr12:87106273-87106283 chr12:87106277-87106287
16	BATF	chr12:87128924-87129189	GM12878	blood:	n/a	chr12:87129029-87129040 chr12:87129124-87129137
17	BATF	chr12:87129654-87130011	GM12878	blood:	n/a	n/a
18	BCL11A	chr12:87129719-87130045	GM12878	blood:	n/a	n/a
19	BCL3	chr12:87105926-87106732	A549	lung:	n/a	chr12:87106275-87106284 chr12:87106276-87106285
20	BCL3	chr12:87129614-87129994	GM12878	blood:	n/a	n/a
21	BCL3	chr12:87220989-87221712	A549	lung:	n/a	n/a
22	BCL3	chr12:87106135-87106543	A549	lung:	n/a	chr12:87106275-87106284 chr12:87106276-87106285
23	BCL3	chr12:87053492-87055044	A549	lung:	n/a	chr12:87053948-87053957
24	BHLHE40	chr12:87219939-87220108	A549	lung:	n/a	n/a
25	BHLHE40	chr12:87222440-87222493	GM12878	blood:	n/a	n/a
26	BRCA1	chr12:87120957-87121494	Hela-S3	cervix:	n/a	n/a
27	BRCA1	chr12:87343121-87343160	Hela-S3	cervix:	n/a	n/a
28	BRCA1	chr12:87340632-87340744	GM12878	blood:	n/a	n/a
29	BRCA1	chr12:87280525-87280594	Hela-S3	cervix:	n/a	n/a
30	BRCA1	chr12:87106043-87106541	Hela-S3	cervix:	n/a	n/a
31	BRCA1	chr12:87297594-87297609	Hela-S3	cervix:	n/a	n/a
32	BRCA1	chr12:87054526-87054996	Hela-S3	cervix:	n/a	n/a
33	CBX3	chr12:87105981-87106752	HCT-116	colon:	n/a	chr12:87106072-87106083
34	CBX3	chr12:87054474-87054921	HCT-116	colon:	n/a	n/a
35	CBX3	chr12:87106000-87106729	HCT-116	colon:	n/a	chr12:87106072-87106083
36	CBX3	chr12:87028429-87028928	HCT-116	colon:	n/a	n/a
37	CEBPB	chr12:87038592-87038865	IMR90	lung:	n/a	n/a
38	CEBPB	chr12:87308490-87308930	MCF-7	breast:	n/a	chr12:87308753-87308764 chr12:87308557-87308568 chr12:87308751-87308764 chr12:87308753-87308764 chr12:87308713-87308726
39	CEBPB	chr12:87308518-87308856	H1-hESC	embryonic stem cell:	n/a	chr12:87308753-87308764 chr12:87308557-87308568 chr12:87308751-87308764 chr12:87308753-87308764 chr12:87308713-87308726
40	CEBPB	chr12:87115484-87115963	ECC-1	luminal epithelium:	n/a	chr12:87115669-87115680
41	CEBPB	chr12:87271059-87271363	A549	lung:	n/a	chr12:87271223-87271236 chr12:87271225-87271234 chr12:87271223-87271236 chr12:87271225-87271236 chr12:87271223-87271234
42	CEBPB	chr12:87129495-87130079	GM12878	blood:	n/a	n/a
43	CEBPB	chr12:86969245-86969329	HepG2	liver:	n/a	chr12:86969264-86969275
44	CEBPB	chr12:87120935-87121500	A549	lung:	n/a	chr12:87121234-87121242
45	CEBPB	chr12:87271066-87271372	K562	blood:	n/a	chr12:87271223-87271236 chr12:87271225-87271234 chr12:87271223-87271236 chr12:87271225-87271236 chr12:87271223-87271234
46	CEBPB	chr12:87007056-87007537	Hela-S3	cervix:	n/a	chr12:87007313-87007324
47	CEBPB	chr12:87169640-87169835	K562	blood:	n/a	chr12:87169695-87169708 chr12:87169695-87169706 chr12:87169697-87169706 chr12:87169695-87169708 chr12:87169697-87169706 chr12:87169714-87169725 chr12:87169697-87169706 chr12:87169697-87169706
48	CEBPB	chr12:87343848-87344183	IMR90	lung:	n/a	chr12:87344011-87344022
49	CEBPB	chr12:87113945-87114196	HepG2	liver:	n/a	chr12:87114098-87114109
50	CEBPB	chr12:87054487-87054984	A549	lung:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:87232692-87232742	AG10803	skin:	n/a
2	chr12:87232692-87232742	AG10803	skin:	n/a
3	chr12:87232511-87232561	MCF-7	breast:	n/a
4	chr12:87119199-87119249	NH-A	brain:	n/a
5	chr12:86994755-86994805	SAEC	small airway:	n/a
6	chr12:87232692-87232742	HL-60	blood:	n/a
7	chr12:87232511-87232561	ECC-1	luminal epithelium:	n/a
8	chr12:87232511-87232561	ProgFib	skin:	n/a
9	chr12:87232692-87232742	CMK	blood:	n/a
10	chr12:87119199-87119249	NHDF-neo	bronchial:	n/a
11	chr12:86994815-86994865	PFSK-1	brain:	n/a
12	chr12:86994755-86994805	Caco-2	colon:	n/a
13	chr12:86995819-86995869	Hela-S3	cervix:	n/a
14	chr12:87119199-87119249	HepG2	liver:	n/a
15	chr12:87106229-87106279	NHDF-neo	bronchial:	n/a
16	chr12:86995819-86995869	LNCaP	prostate:	n/a
17	chr12:87232692-87232742	HPAEpiC	pulmonary alveolar:	n/a
18	chr12:87232692-87232742	MCF10A-Er-Src	breast:	n/a
19	chr12:87232821-87232871	HEK293	kidney:	embryo
20	chr12:87106229-87106279	Hela-S3	cervix:	n/a
21	chr12:86995758-86995808	IMR90	lung:	fetal
22	chr12:86995819-86995869	Caco-2	colon:	n/a
23	chr12:86995819-86995869	BE2_C	brain:	n/a
24	chr12:86995758-86995808	PFSK-1	brain:	n/a
25	chr12:87232692-87232742	GM12878	blood:	n/a
26	chr12:86994755-86994805	SKMC	muscle:	n/a
27	chr12:86995819-86995869	HCPEpiC	choroid plexus:	n/a
28	chr12:86994815-86994865	NHBE	bronchial:	n/a
29	chr12:86995758-86995808	AG10803	skin:	n/a
30	chr12:86995758-86995808	MCF-7	breast:	n/a
31	chr12:86995758-86995808	HMEC	breast:	n/a
32	chr12:86994755-86994805	K562	blood:	n/a
33	chr12:87232511-87232561	Jurkat	blood:	n/a
34	chr12:86995819-86995869	HRPEpiC	eye:	n/a
35	chr12:87106229-87106279	HNPCEpiC	eye:	n/a
36	chr12:86995758-86995808	Hepatocyte	liver:	n/a
37	chr12:87232821-87232871	CMK	blood:	n/a
38	chr12:86995758-86995808	SAEC	small airway:	n/a
39	chr12:87232511-87232561	HIPEpiC	eye:	n/a
40	chr12:87106229-87106279	PFSK-1	brain:	n/a
41	chr12:87232511-87232561	NH-A	brain:	n/a
42	chr12:87232821-87232871	HL-60	blood:	n/a
43	chr12:87106229-87106279	HL-60	blood:	n/a
44	chr12:87106229-87106279	HAEpiC	amniotic membrane:	n/a
45	chr12:87106229-87106279	HMEC	breast:	n/a
46	chr12:87232692-87232742	NHBE	bronchial:	n/a
47	chr12:87119199-87119249	GM06990	blood:	n/a
48	chr12:87232511-87232561	HepG2	liver:	n/a
49	chr12:87106229-87106279	NH-A	brain:	n/a
50	chr12:87119199-87119249	SK-N-SH	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr12:87071567..87073233-chr12:87073299..87075080,2	MCF-7	breast:
2	chr12:87132936..87135299-chr12:87145575..87148336,2	K562	blood:
3	chr12:87148253..87150354-chr12:87164115..87166023,2	MCF-7	breast:
4	chr12:87071567..87073233-chr12:87073299..87075080,2	MCF-7	breast:
5	chr12:87039746..87040275-chr20:55849330..55849889,2	MCF-7	breast:
6	chr12:87237467..87238342-chr7:40961627..40962369,2	MCF-7	breast:
7	chr12:87132936..87135299-chr12:87145575..87148336,2	K562	blood:
8	chr12:87190903..87192895-chr12:87193374..87195934,2	K562	blood:
9	chr12:87190903..87192895-chr12:87193374..87195934,2	K562	blood:
10	chr12:87148253..87150354-chr12:87164115..87166023,2	MCF-7	breast:
11	chr12:87039292..87041386-chr12:87052095..87053649,2	MCF-7	breast:
12	chr12:87039292..87041386-chr12:87052095..87053649,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MGAT4C-3	chr12:87335669-87335818	NONHSAT029768
2	lnc-MGAT4C-1	chr12:86995005-86995081	NONHSAT029759
3	lnc-MGAT4C-1	chr12:87120982-87121018	ENSG00000258185
4	lnc-MGAT4C-1	chr12:86993355-86993438	ENSG00000258185
5	lnc-MGAT4C-1	chr12:87232443-87232905	ENSG00000258185
6	lnc-MGAT4C-3	chr12:87345415-87345519	NONHSAT029768
7	lnc-MGAT4C-1	chr12:87232443-87232775	ENSG00000258185
8	lnc-MGAT4C-1	chr12:87232443-87232681	NONHSAT029762
9	lnc-MGAT4C-1	chr12:87120986-87121018	ENSG00000258185
10	lnc-MGAT4C-1	chr12:86993355-86993438	NONHSAT029759
11	lnc-MGAT4C-1	chr12:87120986-87121018	NONHSAT029762

Variant related genes	Relation type
ENSG00000264077	TF binding region
MGAT4C	TF binding region
ENSG00000258185	TF binding region
ENSG00000264077	CpG island
MGAT4C	CpG island
ENSG00000258185	CpG island

Extended variants
information (count: 5760 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:5760 , 50 per page) page: 1 2 3 4 5 6 7 ... 116

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4508266	chr12:86976237-86976238	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs113410775	chr12:86976268-86976269	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs550527630	chr12:86976304-86976305	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs563858892	chr12:86976316-86976317	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs386764976	chr12:86976322-86976323	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs187705020	chr12:86976324-86976325	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs149974754	chr12:86976406-86976407	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs6144794	chr12:86976418-86976419	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs374921803	chr12:86976419-86976420	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs556799503	chr12:86976438-86976439	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs534809531	chr12:86976509-86976510	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs546662335	chr12:86976517-86976518	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs568521204	chr12:86976566-86976567	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs535516319	chr12:86976568-86976569	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs557315088	chr12:86976571-86976572	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs575495986	chr12:86976586-86976587	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs562497767	chr12:86977138-86977139	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs531122350	chr12:86977178-86977179	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs147670255	chr12:86977259-86977260	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs560652767	chr12:86977282-86977283	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs117242311	chr12:86977334-86977335	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs4374001	chr12:86977367-86977368	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs371226369	chr12:86977371-86977372	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs115329743	chr12:86977378-86977379	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs568501991	chr12:86977385-86977386	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs529386591	chr12:86977398-86977399	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs4508267	chr12:86977399-86977400	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs4359271	chr12:86977440-86977441	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs539759875	chr12:86977507-86977508	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs75124229	chr12:86977511-86977512	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs550643552	chr12:86977523-86977524	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs566750413	chr12:86977534-86977535	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs534011061	chr12:86977568-86977569	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs555526159	chr12:86977634-86977635	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs371673492	chr12:86977693-86977694	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs573699431	chr12:86977710-86977711	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs142592313	chr12:86977769-86977770	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs529854505	chr12:86977812-86977813	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs10858445	chr12:86977825-86977826	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs577541114	chr12:86977833-86977834	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs146904097	chr12:86977941-86977942	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs564476936	chr12:86977973-86977974	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs147968452	chr12:86977977-86977978	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs527476059	chr12:86977994-86977995	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs148977761	chr12:86978026-86978027	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs187465572	chr12:86978027-86978028	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs114145852	chr12:86978028-86978029	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs114426907	chr12:86978040-86978041	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs569179199	chr12:86978053-86978054	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs377186490	chr12:86978116-86978117	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:67)

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
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
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
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	18632612	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	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
Ovarian cancer	21720365	CNVD
Acute myeloid leukemia	20729466	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Renal cell carcinoma	18194544	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	21364760	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Melanoma	17363583	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:501 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:86976200-86976600	Enhancers	Fetal Brain Male	brain
2	chr12:86977000-86977400	Enhancers	Adipose Nuclei	Adipose
3	chr12:86977400-86978400	Weak transcription	Adipose Nuclei	Adipose
4	chr12:86978400-86978600	Enhancers	Adipose Nuclei	Adipose
5	chr12:86994400-86994600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr12:86994600-86994800	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr12:86994600-86994800	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr12:86994800-86995000	Strong transcription	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr12:86994800-86997400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr12:86995000-86996000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr12:86998000-86999200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr12:86998000-86999600	Enhancers	NHEK	skin
13	chr12:86998200-86999000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr12:86999000-86999600	Enhancers	Hela-S3	cervix
15	chr12:87006600-87007800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr12:87006800-87008200	Enhancers	Hela-S3	cervix
17	chr12:87006800-87008200	Enhancers	NHEK	skin
18	chr12:87007600-87008200	Enhancers	Fetal Lung	lung
19	chr12:87016400-87017600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr12:87017600-87018600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr12:87018600-87028200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr12:87028000-87028200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr12:87028000-87029400	Enhancers	Hela-S3	cervix
24	chr12:87028200-87028400	Enhancers	Fetal Brain Male	brain
25	chr12:87028200-87028600	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr12:87028200-87028600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr12:87028200-87029000	Enhancers	HMEC	breast
28	chr12:87028200-87029000	Enhancers	NHEK	skin
29	chr12:87028400-87028800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
30	chr12:87028400-87029000	Enhancers	A549	lung
31	chr12:87028600-87029200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr12:87028600-87030000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr12:87030000-87030200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr12:87040600-87041000	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
35	chr12:87040800-87041400	Enhancers	A549	lung
36	chr12:87041400-87041800	Flanking Active TSS	A549	lung
37	chr12:87041800-87042400	Enhancers	A549	lung
38	chr12:87042400-87052000	Weak transcription	A549	lung
39	chr12:87044000-87044600	Enhancers	HUES48 Cell Line	embryonic stem cell
40	chr12:87051400-87052800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr12:87052000-87053400	Enhancers	A549	lung
42	chr12:87052600-87055600	Enhancers	NHDF-Ad	bronchial
43	chr12:87052600-87058200	Enhancers	Hela-S3	cervix
44	chr12:87052800-87054000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr12:87053400-87054800	Flanking Active TSS	A549	lung
46	chr12:87053800-87055000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
47	chr12:87054000-87054600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
48	chr12:87054000-87054800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr12:87054000-87057600	Enhancers	NHEK	skin
50	chr12:87054400-87054600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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