Variant report

Variant	nsv899050
Chromosome Location	chr12:45299202-45400614
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1081)
CpG islands
(count:184)
Chromatin interactive
region (count:27)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1081 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:45324763-45325169	HepG2	liver:	n/a	n/a
2	ARID3A	chr12:45342480-45342856	HepG2	liver:	n/a	n/a
3	ARID3A	chr12:45324874-45325107	K562	blood:	n/a	n/a
4	ARID3A	chr12:45342536-45342815	K562	blood:	n/a	n/a
5	ATF2	chr12:45342372-45342896	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr12:45342441-45342878	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr12:45342409-45342881	GM12878	blood:	n/a	n/a
8	ATF3	chr12:45342555-45342837	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF3	chr12:45342481-45342790	K562	blood:	n/a	n/a
10	ATF3	chr12:45342450-45342896	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF3	chr12:45342566-45342747	GM12878	blood:	n/a	n/a
12	ATF3	chr12:45342538-45342817	K562	blood:	n/a	n/a
13	ATF3	chr12:45342466-45342882	GM12878	blood:	n/a	n/a
14	ATF3	chr12:45342338-45342894	A549	lung:	n/a	n/a
15	ATF3	chr12:45342372-45342898	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	chr12:45342305-45342894	K562	blood:	n/a	n/a
21	BCLAF1	chr12:45342383-45342868	GM12878	blood:	n/a	n/a
22	BCLAF1	chr12:45342402-45342878	GM12878	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	chr12:45342260-45342982	HCT-116	colon:	n/a	n/a
28	CBX3	chr12:45342312-45342982	HCT-116	colon:	n/a	n/a
29	CBX3	chr12:45342340-45342906	K562	blood:	n/a	n/a
30	CBX3	chr12:45342334-45342817	K562	blood:	n/a	n/a
31	CEBPB	chr12:45385983-45386058	H1-hESC	embryonic stem cell:	n/a	chr12:45386047-45386058
32	CEBPB	chr12:45342484-45342884	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr12:45315256-45315541	HepG2	liver:	n/a	n/a
34	CEBPB	chr12:45324682-45325045	IMR90	lung:	n/a	n/a
35	CEBPB	chr12:45365117-45365119	HepG2	liver:	n/a	n/a
36	CEBPB	chr12:45357525-45357842	A549	lung:	n/a	chr12:45357664-45357675
37	CEBPB	chr12:45315294-45315515	IMR90	lung:	n/a	n/a
38	CEBPB	chr12:45354815-45355057	H1-hESC	embryonic stem cell:	n/a	n/a
39	CEBPB	chr12:45357532-45357836	HepG2	liver:	n/a	chr12:45357664-45357675
40	CEBPB	chr12:45371132-45371228	HepG2	liver:	n/a	chr12:45371152-45371163 chr12:45371150-45371161 chr12:45371150-45371163 chr12:45371152-45371163
41	CEBPB	chr12:45316140-45316203	IMR90	lung:	n/a	n/a
42	CEBPB	chr12:45315262-45315487	A549	lung:	n/a	n/a
43	CEBPB	chr12:45315331-45315529	H1-hESC	embryonic stem cell:	n/a	n/a
44	CEBPB	chr12:45370577-45370777	H1-hESC	embryonic stem cell:	n/a	n/a
45	CEBPB	chr12:45315322-45315505	K562	blood:	n/a	n/a
46	CEBPB	chr12:45371121-45371281	H1-hESC	embryonic stem cell:	n/a	chr12:45371152-45371163 chr12:45371150-45371161 chr12:45371150-45371163 chr12:45371152-45371163
47	CEBPB	chr12:45342469-45342891	H1-hESC	embryonic stem cell:	n/a	n/a
48	CEBPB	chr12:45385948-45386179	HepG2	liver:	n/a	chr12:45386047-45386058
49	CHD1	chr12:45354828-45354850	H1-hESC	embryonic stem cell:	n/a	n/a
50	CHD2	chr12:45342524-45342790	HepG2	liver:	n/a	n/a

(count:184 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:45312146-45312196	U87	brain:	n/a
2	chr12:45312146-45312196	U87	brain:	n/a
3	chr12:45312146-45312196	HRCEpiC	kidney:	n/a
4	chr12:45308058-45308108	HRE	kidney:	n/a
5	chr12:45308058-45308108	HUVEC	blood vessel:	n/a
6	chr12:45312146-45312196	SKMC	muscle:	n/a
7	chr12:45354182-45354232	HCPEpiC	choroid plexus:	n/a
8	chr12:45354182-45354232	HEEpiC	esophagus:	n/a
9	chr12:45354182-45354232	GM19239	blood:	n/a
10	chr12:45308058-45308108	AG09319	gingival:	n/a
11	chr12:45354182-45354232	ovcar-3	ovarian:	n/a
12	chr12:45308058-45308108	HCM	heart:	n/a
13	chr12:45354182-45354232	HRCEpiC	kidney:	n/a
14	chr12:45308058-45308108	MCF-7	breast:	n/a
15	chr12:45354182-45354232	HNPCEpiC	eye:	n/a
16	chr12:45308058-45308108	IMR90	lung:	fetal
17	chr12:45308058-45308108	K562	blood:	n/a
18	chr12:45312146-45312196	AG04450	lung:	fetal
19	chr12:45308058-45308108	AG04449	skin:	fetal
20	chr12:45312146-45312196	PANC-1	pancreas:	n/a
21	chr12:45308058-45308108	NHBE	bronchial:	n/a
22	chr12:45312146-45312196	ProgFib	skin:	n/a
23	chr12:45354182-45354232	LNCaP	prostate:	n/a
24	chr12:45308058-45308108	Hela-S3	cervix:	n/a
25	chr12:45308058-45308108	HMEC	breast:	n/a
26	chr12:45308058-45308108	Caco-2	colon:	n/a
27	chr12:45308058-45308108	RPTEC	kidney:	n/a
28	chr12:45308058-45308108	SAEC	small airway:	n/a
29	chr12:45308058-45308108	SK-N-SH	brain:	n/a
30	chr12:45312146-45312196	RPTEC	kidney:	n/a
31	chr12:45312146-45312196	AG10803	skin:	n/a
32	chr12:45308058-45308108	LNCaP	prostate:	n/a
33	chr12:45308058-45308108	HNPCEpiC	eye:	n/a
34	chr12:45308058-45308108	GM06990	blood:	n/a
35	chr12:45312146-45312196	HepG2	liver:	n/a
36	chr12:45308058-45308108	BJ	skin:	n/a
37	chr12:45308058-45308108	HCF	heart:	n/a
38	chr12:45312146-45312196	ECC-1	luminal epithelium:	n/a
39	chr12:45312146-45312196	T-47D	breast:	n/a
40	chr12:45308058-45308108	ECC-1	luminal epithelium:	n/a
41	chr12:45312146-45312196	HCF	heart:	n/a
42	chr12:45308058-45308108	HL-60	blood:	n/a
43	chr12:45308058-45308108	HEEpiC	esophagus:	n/a
44	chr12:45308058-45308108	ovcar-3	ovarian:	n/a
45	chr12:45312146-45312196	GM12892	blood:	n/a
46	chr12:45354182-45354232	SAEC	small airway:	n/a
47	chr12:45312146-45312196	NT2-D1	testis:	n/a
48	chr12:45308058-45308108	HRPEpiC	eye:	n/a
49	chr12:45312146-45312196	SK-N-SH_RA	brain:	n/a
50	chr12:45312146-45312196	MCF-7	breast:	n/a

(count:27 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:45356113..45357820-chr12:45366859..45369459,2	K562	blood:
2	chr12:44152736..44154248-chr12:45340094..45342820,2	K562	blood:
3	chr1:241803684..241804232-chr12:45354058..45354559,2	Hela-S3	cervix:
4	chr12:45367140..45370350-chr12:45371616..45375145,3	K562	blood:
5	chr12:45336563..45338424-chr12:45340632..45342622,2	K562	blood:
6	chr12:45206023..45206756-chr12:45324521..45325295,2	MCF-7	breast:
7	chr12:45367140..45370350-chr12:45371616..45375145,3	K562	blood:
8	chr12:45336563..45338424-chr12:45340632..45342622,2	K562	blood:
9	chr12:44351332..44351888-chr12:45342306..45343125,2	MCF-7	breast:
10	chr12:45366306..45367231-chr12:45516422..45517207,2	MCF-7	breast:
11	chr12:45342516..45343191-chr20:52556232..52556957,2	MCF-7	breast:
12	chr12:45342246..45343064-chr12:45516256..45517072,4	MCF-7	breast:
13	chr12:45168298..45169262-chr12:45324213..45325460,5	MCF-7	breast:
14	chr12:44409231..44409847-chr12:45324739..45325375,2	MCF-7	breast:
15	chr12:45366332..45368097-chr12:45514780..45516888,12	MCF-7	breast:
16	chr12:44396911..44397707-chr12:45324896..45325406,2	MCF-7	breast:
17	chr12:45342229..45343064-chr12:45516341..45517152,5	MCF-7	breast:
18	chr12:45168329..45169564-chr12:45323968..45325348,4	K562	blood:
19	chr12:45356113..45357820-chr12:45366859..45369459,2	K562	blood:
20	chr12:45342280..45342887-chr12:45354890..45355754,2	MCF-7	breast:
21	chr12:44393933..44394766-chr12:45324489..45325458,2	MCF-7	breast:
22	chr12:45341565..45342209-chr12:45516342..45517228,2	MCF-7	breast:
23	chr1:114889023..114889538-chr12:45342253..45342809,2	MCF-7	breast:
24	chr12:45364370..45366746-chr12:45513644..45516185,2	MCF-7	breast:
25	chr12:45342280..45342887-chr12:45354890..45355754,2	MCF-7	breast:
26	chr12:44351426..44352202-chr12:45324508..45325417,2	K562	blood:
27	chr12:44393907..44394577-chr12:45342454..45343052,2	MCF-7	breast:

No data

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

Extended variants
information (count: 1253 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:1253 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs138743076	chr12:45307713-45307714	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs193135057	chr12:45307721-45307722	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs557801326	chr12:45307752-45307753	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs576299985	chr12:45307766-45307767	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs368149712	chr12:45307893-45307894	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs11182742	chr12:45307899-45307900	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs573636011	chr12:45307923-45307924	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs415380	chr12:45308074-45308075	Inactive region	CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs144668565	chr12:45308092-45308093	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
10	rs77021787	chr12:45309110-45309111	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs145455842	chr12:45309160-45309161	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs373105833	chr12:45309185-45309186	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs77797007	chr12:45309224-45309225	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs376544216	chr12:45309289-45309290	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs144309879	chr12:45309369-45309370	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs148862703	chr12:45309378-45309379	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs538737196	chr12:45309404-45309405	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs73283039	chr12:45309416-45309417	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs576603649	chr12:45309542-45309543	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs563010470	chr12:45309568-45309569	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs138041837	chr12:45309575-45309576	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs536699600	chr12:45309577-45309578	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs201731081	chr12:45309592-45309593	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs421642	chr12:45309615-45309616	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs12832449	chr12:45309691-45309692	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs12809245	chr12:45309692-45309693	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs12814022	chr12:45309712-45309713	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs12814026	chr12:45309714-45309715	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs373440958	chr12:45309729-45309730	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs12811873	chr12:45309731-45309732	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs555505986	chr12:45309736-45309737	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs574015915	chr12:45309744-45309745	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs541277716	chr12:45309748-45309749	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs73283041	chr12:45309771-45309772	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs533162819	chr12:45309799-45309800	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs12814186	chr12:45309810-45309811	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs12819158	chr12:45309811-45309812	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs141031568	chr12:45309848-45309849	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs189406828	chr12:45309849-45309850	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs563611051	chr12:45309894-45309895	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs75163545	chr12:45309904-45309905	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs548923047	chr12:45309922-45309923	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs567441021	chr12:45309943-45309944	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs528398901	chr12:45309948-45309949	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs74778310	chr12:45309955-45309956	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs571305638	chr12:45309973-45309974	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs182237337	chr12:45309986-45309987	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs425857	chr12:45310031-45310032	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs549267758	chr12:45310066-45310067	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs144753111	chr12:45310069-45310070	Inactive region	TF binding region	1 gene(s)	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:108 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:45311000-45312200	Enhancers	iPS-15b Cell Line	embryonic stem cell
2	chr12:45311800-45312000	Enhancers	HUES48 Cell Line	embryonic stem cell
3	chr12:45312600-45312800	Enhancers	HUES48 Cell Line	embryonic stem cell
4	chr12:45313200-45313600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr12:45315000-45315600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr12:45315000-45315600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr12:45322600-45325000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr12:45322800-45323800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
9	chr12:45323000-45323600	Enhancers	Brain Germinal Matrix	brain
10	chr12:45323000-45323800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr12:45323000-45323800	Enhancers	Fetal Brain Female	brain
12	chr12:45323200-45323400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr12:45323200-45323600	Enhancers	Primary hematopoietic stem cells	blood
14	chr12:45323400-45324200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr12:45323600-45325000	Enhancers	Fetal Brain Male	brain
16	chr12:45323800-45324200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
17	chr12:45323800-45324200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr12:45324200-45324600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
19	chr12:45324200-45325000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr12:45324200-45325000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr12:45324400-45324800	Enhancers	HUVEC	blood vessel
22	chr12:45324400-45325000	Enhancers	Primary T cells from cord blood	blood
23	chr12:45324400-45325000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
24	chr12:45336400-45337000	Enhancers	HepG2	liver
25	chr12:45336400-45337600	Enhancers	Fetal Intestine Large	intestine
26	chr12:45336600-45337000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr12:45336600-45337200	Enhancers	Liver	Liver
28	chr12:45337000-45342400	Weak transcription	HepG2	liver
29	chr12:45340200-45340600	Enhancers	iPS-15b Cell Line	embryonic stem cell
30	chr12:45340200-45341600	Enhancers	HUES48 Cell Line	embryonic stem cell
31	chr12:45340400-45340800	Enhancers	iPS-18 Cell Line	embryonic stem cell
32	chr12:45340600-45341000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
33	chr12:45340600-45341200	Enhancers	HUES6 Cell Line	embryonic stem cell
34	chr12:45340600-45341600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
35	chr12:45340800-45341000	Enhancers	iPS-20b Cell Line	embryonic stem cell
36	chr12:45340800-45341400	Enhancers	HUES64 Cell Line	embryonic stem cell
37	chr12:45340800-45342200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
38	chr12:45341000-45341200	Enhancers	iPS-15b Cell Line	embryonic stem cell
39	chr12:45341000-45341400	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
40	chr12:45341200-45342200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
41	chr12:45341200-45342400	Weak transcription	HUES6 Cell Line	embryonic stem cell
42	chr12:45341400-45342200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
43	chr12:45342200-45342400	Active TSS	A549	lung
44	chr12:45342200-45342400	Bivalent Enhancer	Dnd41	blood
45	chr12:45342200-45342400	Active TSS	Hela-S3	cervix
46	chr12:45342200-45342600	Active TSS	iPS-15b Cell Line	embryonic stem cell
47	chr12:45342200-45342600	Active TSS	iPS-20b Cell Line	embryonic stem cell
48	chr12:45342200-45342600	Active TSS	K562	blood
49	chr12:45342200-45342800	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr12:45342400-45342600	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell

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