Variant report

Variant	nsv527565
Chromosome Location	chr12:45319767-45365812
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:814)
CpG islands
(count:61)
Chromatin interactive
region (count:22)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:814 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:45342536-45342815	K562	blood:	n/a	n/a
2	ARID3A	chr12:45324763-45325169	HepG2	liver:	n/a	n/a
3	ARID3A	chr12:45342480-45342856	HepG2	liver:	n/a	n/a
4	ARID3A	chr12:45324874-45325107	K562	blood:	n/a	n/a
5	ATF2	chr12:45342441-45342878	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr12:45342409-45342881	GM12878	blood:	n/a	n/a
7	ATF2	chr12:45342372-45342896	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF3	chr12:45342372-45342898	A549	lung:	n/a	n/a
9	ATF3	chr12:45342538-45342817	K562	blood:	n/a	n/a
10	ATF3	chr12:45342555-45342837	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF3	chr12:45342566-45342747	GM12878	blood:	n/a	n/a
12	ATF3	chr12:45342450-45342896	H1-hESC	embryonic stem cell:	n/a	n/a
13	ATF3	chr12:45342466-45342882	GM12878	blood:	n/a	n/a
14	ATF3	chr12:45342481-45342790	K562	blood:	n/a	n/a
15	ATF3	chr12:45342338-45342894	A549	lung:	n/a	n/a
16	BACH1	chr12:45342470-45342698	K562	blood:	n/a	n/a
17	BACH1	chr12:45354798-45354985	H1-hESC	embryonic stem cell:	n/a	n/a
18	BATF	chr12:45342457-45342679	GM12878	blood:	n/a	n/a
19	BCL3	chr12:45342273-45342920	A549	lung:	n/a	n/a
20	BCLAF1	chr12:45342383-45342868	GM12878	blood:	n/a	n/a
21	BCLAF1	chr12:45342402-45342878	GM12878	blood:	n/a	n/a
22	BCLAF1	chr12:45342305-45342894	K562	blood:	n/a	n/a
23	BCLAF1	chr12:45342419-45342837	K562	blood:	n/a	n/a
24	BHLHE40	chr12:45342454-45342812	K562	blood:	n/a	n/a
25	BRCA1	chr12:45342410-45342819	H1-hESC	embryonic stem cell:	n/a	n/a
26	BRCA1	chr12:45342492-45342826	Hela-S3	cervix:	n/a	n/a
27	CBX3	chr12:45342340-45342906	K562	blood:	n/a	n/a
28	CBX3	chr12:45342260-45342982	HCT-116	colon:	n/a	n/a
29	CBX3	chr12:45342334-45342817	K562	blood:	n/a	n/a
30	CBX3	chr12:45342312-45342982	HCT-116	colon:	n/a	n/a
31	CEBPB	chr12:45342484-45342884	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chr12:45357525-45357842	A549	lung:	n/a	chr12:45357664-45357675
33	CEBPB	chr12:45357532-45357836	HepG2	liver:	n/a	chr12:45357664-45357675
34	CEBPB	chr12:45342469-45342891	H1-hESC	embryonic stem cell:	n/a	n/a
35	CEBPB	chr12:45324682-45325045	IMR90	lung:	n/a	n/a
36	CEBPB	chr12:45354815-45355057	H1-hESC	embryonic stem cell:	n/a	n/a
37	CEBPB	chr12:45365117-45365119	HepG2	liver:	n/a	n/a
38	CHD1	chr12:45354828-45354850	H1-hESC	embryonic stem cell:	n/a	n/a
39	CHD2	chr12:45342405-45342845	Hela-S3	cervix:	n/a	n/a
40	CHD2	chr12:45342499-45342783	K562	blood:	n/a	n/a
41	CHD2	chr12:45342387-45342869	H1-hESC	embryonic stem cell:	n/a	n/a
42	CHD2	chr12:45342524-45342790	HepG2	liver:	n/a	n/a
43	CREB1	chr12:45342459-45342868	A549	lung:	n/a	n/a
44	CREB1	chr12:45342367-45342920	H1-hESC	embryonic stem cell:	n/a	n/a
45	CTBP2	chr12:45342450-45342939	H1-hESC	embryonic stem cell:	n/a	n/a
46	CTCF	chr12:45324940-45325090	HCT-116	colon:	n/a	chr12:45324976-45324989 chr12:45324969-45324990 chr12:45324974-45324992 chr12:45324975-45324991
47	CTCF	chr12:45354760-45354910	GM12875	blood:	n/a	n/a
48	CTCF	chr12:45324940-45325090	HPAF	blood vessel:	n/a	chr12:45324976-45324989 chr12:45324969-45324990 chr12:45324974-45324992 chr12:45324975-45324991
49	CTCF	chr12:45342093-45344030	A549	lung:	n/a	chr12:45342681-45342702 chr12:45342682-45342691 chr12:45342709-45342730 chr12:45342679-45342697 chr12:45342716-45342729 chr12:45342714-45342732
50	CTCF	chr12:45342660-45342810	MCF-7	breast:	n/a	chr12:45342681-45342702 chr12:45342682-45342691 chr12:45342709-45342730 chr12:45342679-45342697 chr12:45342716-45342729 chr12:45342714-45342732

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:45354182-45354232	ovcar-3	ovarian:	n/a
2	chr12:45354182-45354232	HUVEC	blood vessel:	n/a
3	chr12:45354182-45354232	K562	blood:	n/a
4	chr12:45354182-45354232	AG09319	gingival:	n/a
5	chr12:45354182-45354232	MCF10A-Er-Src	breast:	n/a
6	chr12:45354182-45354232	Jurkat	blood:	n/a
7	chr12:45354182-45354232	NB4	blood:	n/a
8	chr12:45354182-45354232	HRE	kidney:	n/a
9	chr12:45354182-45354232	NH-A	brain:	n/a
10	chr12:45354182-45354232	SK-N-SH_RA	brain:	n/a
11	chr12:45354182-45354232	Caco-2	colon:	n/a
12	chr12:45354182-45354232	NHBE	bronchial:	n/a
13	chr12:45354182-45354232	Hepatocyte	liver:	n/a
14	chr12:45354182-45354232	RPTEC	kidney:	n/a
15	chr12:45354182-45354232	AG04450	lung:	fetal
16	chr12:45354182-45354232	BJ	skin:	n/a
17	chr12:45354182-45354232	PANC-1	pancreas:	n/a
18	chr12:45354182-45354232	SK-N-SH	brain:	n/a
19	chr12:45354182-45354232	GM06990	blood:	n/a
20	chr12:45354182-45354232	HCF	heart:	n/a
21	chr12:45354182-45354232	AG09309	skin:	n/a
22	chr12:45354182-45354232	PFSK-1	brain:	n/a
23	chr12:45354182-45354232	HCPEpiC	choroid plexus:	n/a
24	chr12:45354182-45354232	AG04449	skin:	fetal
25	chr12:45354182-45354232	Hela-S3	cervix:	n/a
26	chr12:45354182-45354232	NHDF-neo	bronchial:	n/a
27	chr12:45354182-45354232	HepG2	liver:	n/a
28	chr12:45354182-45354232	HCM	heart:	n/a
29	chr12:45354182-45354232	GM12878	blood:	n/a
30	chr12:45354182-45354232	HRPEpiC	eye:	n/a
31	chr12:45354182-45354232	HIPEpiC	eye:	n/a
32	chr12:45354182-45354232	MCF-7	breast:	n/a
33	chr12:45354182-45354232	ECC-1	luminal epithelium:	n/a
34	chr12:45354182-45354232	A549	lung:	n/a
35	chr12:45354182-45354232	HRCEpiC	kidney:	n/a
36	chr12:45354182-45354232	HEK293	kidney:	embryo
37	chr12:45354182-45354232	GM19239	blood:	n/a
38	chr12:45354182-45354232	GM12892	blood:	n/a
39	chr12:45354182-45354232	HPAEpiC	pulmonary alveolar:	n/a
40	chr12:45354182-45354232	U87	brain:	n/a
41	chr12:45354182-45354232	GM12891	blood:	n/a
42	chr12:45354182-45354232	HMEC	breast:	n/a
43	chr12:45354182-45354232	PrEC	prostate:	n/a
44	chr12:45354182-45354232	T-47D	breast:	n/a
45	chr12:45354182-45354232	ProgFib	skin:	n/a
46	chr12:45354182-45354232	AoSMC	blood vessel:	n/a
47	chr12:45354182-45354232	SK-N-MC	brain:	n/a
48	chr12:45354182-45354232	NT2-D1	testis:	n/a
49	chr12:45354182-45354232	SAEC	small airway:	n/a
50	chr12:45354182-45354232	IMR90	lung:	fetal

(count:22 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:241803684..241804232-chr12:45354058..45354559,2	Hela-S3	cervix:
2	chr12:45342280..45342887-chr12:45354890..45355754,2	MCF-7	breast:
3	chr12:45336563..45338424-chr12:45340632..45342622,2	K562	blood:
4	chr12:44152736..44154248-chr12:45340094..45342820,2	K562	blood:
5	chr12:44351426..44352202-chr12:45324508..45325417,2	K562	blood:
6	chr12:45356113..45357820-chr12:45366859..45369459,2	K562	blood:
7	chr12:45364370..45366746-chr12:45513644..45516185,2	MCF-7	breast:
8	chr12:44351332..44351888-chr12:45342306..45343125,2	MCF-7	breast:
9	chr12:45206023..45206756-chr12:45324521..45325295,2	MCF-7	breast:
10	chr12:44393907..44394577-chr12:45342454..45343052,2	MCF-7	breast:
11	chr12:44393933..44394766-chr12:45324489..45325458,2	MCF-7	breast:
12	chr12:45168298..45169262-chr12:45324213..45325460,5	MCF-7	breast:
13	chr12:45168329..45169564-chr12:45323968..45325348,4	K562	blood:
14	chr12:45342516..45343191-chr20:52556232..52556957,2	MCF-7	breast:
15	chr12:45342246..45343064-chr12:45516256..45517072,4	MCF-7	breast:
16	chr12:44409231..44409847-chr12:45324739..45325375,2	MCF-7	breast:
17	chr12:44396911..44397707-chr12:45324896..45325406,2	MCF-7	breast:
18	chr12:45341565..45342209-chr12:45516342..45517228,2	MCF-7	breast:
19	chr12:45342280..45342887-chr12:45354890..45355754,2	MCF-7	breast:
20	chr12:45342229..45343064-chr12:45516341..45517152,5	MCF-7	breast:
21	chr12:45336563..45338424-chr12:45340632..45342622,2	K562	blood:
22	chr1:114889023..114889538-chr12:45342253..45342809,2	MCF-7	breast:

No data

Variant related genes	Relation type
NELL2	TF binding region
NELL2	CpG island
ENSG00000198001	chromatin interactions
ENSG00000054277	chromatin interactions
ENSG00000236352	chromatin interactions

Extended variants
information (count: 583 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:583 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs565516888	chr12:45320435-45320436	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs574057974	chr12:45322605-45322606	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs541503262	chr12:45322612-45322613	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs559329993	chr12:45322621-45322622	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs191389934	chr12:45322626-45322627	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs142635995	chr12:45322629-45322630	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs563589721	chr12:45322646-45322647	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs530798180	chr12:45322669-45322670	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs549003010	chr12:45322711-45322712	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs567214828	chr12:45322748-45322749	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs150981680	chr12:45322795-45322796	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs7975618	chr12:45322838-45322839	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs73090909	chr12:45322842-45322843	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs566172133	chr12:45322848-45322849	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs530502545	chr12:45322858-45322859	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs552231890	chr12:45322914-45322915	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs17598279	chr12:45322915-45322916	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs444468	chr12:45322922-45322923	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs373785554	chr12:45322929-45322930	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs576329213	chr12:45322943-45322944	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs537304535	chr12:45322951-45322952	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs184138190	chr12:45322963-45322964	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs573972246	chr12:45322967-45322968	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs541193934	chr12:45322996-45322997	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs543217568	chr12:45323031-45323032	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs553414981	chr12:45323064-45323065	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs546734516	chr12:45323124-45323125	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs578118585	chr12:45323139-45323140	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs545245083	chr12:45323145-45323146	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs568168436	chr12:45323149-45323150	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs376992795	chr12:45323151-45323152	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs530835878	chr12:45323173-45323174	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs535690903	chr12:45323316-45323317	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs73090910	chr12:45323366-45323367	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs540525895	chr12:45323368-45323369	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs369557340	chr12:45323406-45323407	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs78442934	chr12:45323449-45323450	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs77923282	chr12:45323497-45323498	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs385152	chr12:45323521-45323522	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs395519	chr12:45323530-45323531	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs371403806	chr12:45323531-45323532	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs548386189	chr12:45323581-45323582	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs373268881	chr12:45323695-45323696	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs569903983	chr12:45323731-45323732	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs569850942	chr12:45323752-45323753	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs73284986	chr12:45323813-45323814	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs189070029	chr12:45323849-45323850	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs193045850	chr12:45323874-45323875	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs537018028	chr12:45323901-45323902	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs558542315	chr12:45323903-45323904	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:67)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Seminomas	18059402	CNVD
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
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Neurodevelopmental disorder	22521361	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Renal cell carcinoma	18194544	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
Hirschsprung''s Disease	21712996	CNVD
Lissencephaly	21572526	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Breast cancer	19602461	CNVD
Breast cancer	17899364	CNVD
Colorectal cancer	16272173	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Cancer	20164919	CNVD
Adenoid cystic carcinoma	18332873	CNVD
Breast cancer	21364760	CNVD
Prostate cancer	18632612	CNVD
Gastric cancer	18160780	CNVD
Myelofibrosis	22110671	CNVD
Follicular lymphoma	20505157	CNVD
Hepatocellular carcinoma	16750200	CNVD
Melanoma	18172304	CNVD
Metanephric adenoma	20802469	CNVD
Glioblastoma multiforme	17387387	CNVD
liposarcomas	17372913	CNVD
Non-small cell lung cancer	24170126	CNVD
Cancer	16751803	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:88 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:45322600-45325000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr12:45322800-45323800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chr12:45323000-45323600	Enhancers	Brain Germinal Matrix	brain
4	chr12:45323000-45323800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr12:45323000-45323800	Enhancers	Fetal Brain Female	brain
6	chr12:45323200-45323400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr12:45323200-45323600	Enhancers	Primary hematopoietic stem cells	blood
8	chr12:45323400-45324200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr12:45323600-45325000	Enhancers	Fetal Brain Male	brain
10	chr12:45323800-45324200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
11	chr12:45323800-45324200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr12:45324200-45324600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr12:45324200-45325000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr12:45324200-45325000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr12:45324400-45324800	Enhancers	HUVEC	blood vessel
16	chr12:45324400-45325000	Enhancers	Primary T cells from cord blood	blood
17	chr12:45324400-45325000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
18	chr12:45336400-45337000	Enhancers	HepG2	liver
19	chr12:45336400-45337600	Enhancers	Fetal Intestine Large	intestine
20	chr12:45336600-45337000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr12:45336600-45337200	Enhancers	Liver	Liver
22	chr12:45337000-45342400	Weak transcription	HepG2	liver
23	chr12:45340200-45340600	Enhancers	iPS-15b Cell Line	embryonic stem cell
24	chr12:45340200-45341600	Enhancers	HUES48 Cell Line	embryonic stem cell
25	chr12:45340400-45340800	Enhancers	iPS-18 Cell Line	embryonic stem cell
26	chr12:45340600-45341000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
27	chr12:45340600-45341200	Enhancers	HUES6 Cell Line	embryonic stem cell
28	chr12:45340600-45341600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
29	chr12:45340800-45341000	Enhancers	iPS-20b Cell Line	embryonic stem cell
30	chr12:45340800-45341400	Enhancers	HUES64 Cell Line	embryonic stem cell
31	chr12:45340800-45342200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
32	chr12:45341000-45341200	Enhancers	iPS-15b Cell Line	embryonic stem cell
33	chr12:45341000-45341400	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
34	chr12:45341200-45342200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
35	chr12:45341200-45342400	Weak transcription	HUES6 Cell Line	embryonic stem cell
36	chr12:45341400-45342200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
37	chr12:45342200-45342400	Active TSS	A549	lung
38	chr12:45342200-45342400	Bivalent Enhancer	Dnd41	blood
39	chr12:45342200-45342400	Active TSS	Hela-S3	cervix
40	chr12:45342200-45342600	Active TSS	iPS-15b Cell Line	embryonic stem cell
41	chr12:45342200-45342600	Active TSS	iPS-20b Cell Line	embryonic stem cell
42	chr12:45342200-45342600	Active TSS	K562	blood
43	chr12:45342200-45342800	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr12:45342400-45342600	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
45	chr12:45342400-45342600	Enhancers	iPS-18 Cell Line	embryonic stem cell
46	chr12:45342400-45342600	Enhancers	Primary T killer memory cells from peripheral blood	blood
47	chr12:45342400-45342600	Flanking Active TSS	Liver	Liver
48	chr12:45342400-45342600	Enhancers	Lung	lung
49	chr12:45342400-45342600	Flanking Active TSS	A549	lung
50	chr12:45342400-45342600	Flanking Bivalent TSS/Enh	Dnd41	blood

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