Variant report

Variant	nsv899062
Chromosome Location	chr12:48658212-48711867
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:482)
CpG islands
(count:306)
Chromatin interactive
region (count:40)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:482 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:48705888-48706088	K562	blood:	n/a	n/a
2	ARID3A	chr12:48690330-48690598	K562	blood:	n/a	n/a
3	ARID3A	chr12:48697810-48697842	K562	blood:	n/a	n/a
4	ATF1	chr12:48690322-48690656	K562	blood:	n/a	n/a
5	ATF1	chr12:48675696-48675870	K562	blood:	n/a	n/a
6	ATF1	chr12:48705130-48705435	K562	blood:	n/a	n/a
7	BACH1	chr12:48690123-48690696	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr12:48690232-48690618	K562	blood:	n/a	n/a
9	BHLHE40	chr12:48690282-48690694	K562	blood:	n/a	n/a
10	BHLHE40	chr12:48705147-48705397	K562	blood:	n/a	n/a
11	CBX3	chr12:48670467-48670726	K562	blood:	n/a	n/a
12	CBX3	chr12:48690262-48690833	K562	blood:	n/a	n/a
13	CBX3	chr12:48705078-48705457	K562	blood:	n/a	n/a
14	CBX3	chr12:48670479-48670716	K562	blood:	n/a	n/a
15	CCNT2	chr12:48690467-48690661	K562	blood:	n/a	n/a
16	CCNT2	chr12:48705180-48705450	K562	blood:	n/a	n/a
17	CEBPB	chr12:48693069-48693135	K562	blood:	n/a	n/a
18	CEBPB	chr12:48691677-48691895	K562	blood:	n/a	n/a
19	CEBPB	chr12:48685858-48686172	K562	blood:	n/a	n/a
20	CEBPB	chr12:48672987-48673226	MCF-7	breast:	n/a	n/a
21	CEBPB	chr12:48676827-48676839	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr12:48685953-48686039	A549	lung:	n/a	n/a
23	CEBPD	chr12:48705016-48705493	K562	blood:	n/a	n/a
24	CHD2	chr12:48690402-48690644	K562	blood:	n/a	n/a
25	CREB1	chr12:48690377-48690682	A549	lung:	n/a	n/a
26	CTCF	chr12:48680540-48680690	AG09309	skin:	n/a	chr12:48680655-48680668
27	CTCF	chr12:48680160-48680310	BE2_C	brain:	n/a	n/a
28	CTCF	chr12:48680600-48680750	K562	blood:	n/a	chr12:48680655-48680668
29	CTCF	chr12:48680580-48680730	HVMF	connective:	n/a	chr12:48680655-48680668
30	CTCF	chr12:48680600-48680750	HEK293	kidney:	n/a	chr12:48680655-48680668
31	CTCF	chr12:48690440-48690590	HCPEpiC	choroid plexus:	n/a	n/a
32	CTCF	chr12:48693812-48693814	Spleen_OC	spleen:	n/a	n/a
33	CTCF	chr12:48680600-48680750	GM12865	blood:	n/a	chr12:48680655-48680668
34	CTCF	chr12:48680580-48680730	NHEK	skin:	n/a	chr12:48680655-48680668
35	CTCF	chr12:48690300-48690450	HMEC	breast:	n/a	n/a
36	CTCF	chr12:48680620-48680770	GM12866	blood:	n/a	chr12:48680655-48680668
37	CTCF	chr12:48680580-48680730	BJ	skin:	n/a	chr12:48680655-48680668
38	CTCF	chr12:48680593-48680692	GM13976	blood:	n/a	chr12:48680655-48680668
39	CTCF	chr12:48680560-48680710	GM12864	blood:	n/a	chr12:48680655-48680668
40	CTCF	chr12:48680600-48680750	GM12872	blood:	n/a	chr12:48680655-48680668
41	CTCF	chr12:48680580-48680730	HA-sp	spinal cord:	n/a	chr12:48680655-48680668
42	CTCF	chr12:48680456-48680882	HCT-116	colon:	n/a	chr12:48680655-48680668
43	CTCF	chr12:48680480-48680630	HMEC	breast:	n/a	n/a
44	CTCF	chr12:48680540-48680690	HBMEC	blood vessel:	n/a	chr12:48680655-48680668
45	CTCF	chr12:48680583-48680721	NHEK	skin:	n/a	chr12:48680655-48680668
46	CTCF	chr12:48680314-48680356	GM10248	blood:	n/a	n/a
47	CTCF	chr12:48680577-48680722	Fibrobl	skin:	n/a	chr12:48680655-48680668
48	CTCF	chr12:48680620-48680770	HRE	kidney:	n/a	chr12:48680655-48680668
49	CTCF	chr12:48680540-48680690	SK-N-SH_RA	brain:	n/a	chr12:48680655-48680668
50	CTCF	chr12:48680580-48680730	HBMEC	blood vessel:	n/a	chr12:48680655-48680668

(count:306 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:48690546-48690596	HEK293	kidney:	embryo
2	chr12:48690546-48690596	HEK293	kidney:	embryo
3	chr12:48690915-48690965	AG10803	skin:	n/a
4	chr12:48690915-48690965	HRCEpiC	kidney:	n/a
5	chr12:48690689-48690739	A549	lung:	n/a
6	chr12:48691036-48691086	Caco-2	colon:	n/a
7	chr12:48690546-48690596	HMEC	breast:	n/a
8	chr12:48690974-48691024	PFSK-1	brain:	n/a
9	chr12:48691036-48691086	MCF-7	breast:	n/a
10	chr12:48691036-48691086	AG09319	gingival:	n/a
11	chr12:48690915-48690965	NB4	blood:	n/a
12	chr12:48690546-48690596	HCPEpiC	choroid plexus:	n/a
13	chr12:48690974-48691024	NHBE	bronchial:	n/a
14	chr12:48690974-48691024	AG04449	skin:	fetal
15	chr12:48690689-48690739	GM12878	blood:	n/a
16	chr12:48690974-48691024	HRE	kidney:	n/a
17	chr12:48690974-48691024	HCM	heart:	n/a
18	chr12:48690546-48690596	H1-hESC	embryonic stem cell:	embryo
19	chr12:48690915-48690965	PANC-1	pancreas:	n/a
20	chr12:48691036-48691086	SAEC	small airway:	n/a
21	chr12:48690915-48690965	HUVEC	blood vessel:	n/a
22	chr12:48690915-48690965	NH-A	brain:	n/a
23	chr12:48690974-48691024	SKMC	muscle:	n/a
24	chr12:48690974-48691024	PANC-1	pancreas:	n/a
25	chr12:48690689-48690739	HCPEpiC	choroid plexus:	n/a
26	chr12:48690974-48691024	Hepatocyte	liver:	n/a
27	chr12:48690915-48690965	U87	brain:	n/a
28	chr12:48690974-48691024	HL-60	blood:	n/a
29	chr12:48690689-48690739	HepG2	liver:	n/a
30	chr12:48690546-48690596	NB4	blood:	n/a
31	chr12:48690546-48690596	NT2-D1	testis:	n/a
32	chr12:48690915-48690965	HCM	heart:	n/a
33	chr12:48691036-48691086	GM06990	blood:	n/a
34	chr12:48690974-48691024	CMK	blood:	n/a
35	chr12:48690974-48691024	SK-N-SH_RA	brain:	n/a
36	chr12:48690546-48690596	HRCEpiC	kidney:	n/a
37	chr12:48691036-48691086	GM12878	blood:	n/a
38	chr12:48690915-48690965	BJ	skin:	n/a
39	chr12:48691036-48691086	HRPEpiC	eye:	n/a
40	chr12:48690915-48690965	RPTEC	kidney:	n/a
41	chr12:48691036-48691086	LNCaP	prostate:	n/a
42	chr12:48690974-48691024	U87	brain:	n/a
43	chr12:48690915-48690965	A549	lung:	n/a
44	chr12:48691036-48691086	ovcar-3	ovarian:	n/a
45	chr12:48690689-48690739	HUVEC	blood vessel:	n/a
46	chr12:48690974-48691024	AG09319	gingival:	n/a
47	chr12:48690689-48690739	HRPEpiC	eye:	n/a
48	chr12:48690915-48690965	GM12892	blood:	n/a
49	chr12:48690546-48690596	AG04450	lung:	fetal
50	chr12:48690689-48690739	HIPEpiC	eye:	n/a

(count:40 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:48593487..48595723-chr12:48689162..48691231,3	K562	blood:
2	chr12:48680248..48681138-chr12:48730039..48730595,2	MCF-7	breast:
3	chr12:48698712..48702509-chr12:48702715..48705745,3	MCF-7	breast:
4	chr12:48704261..48706305-chr12:48731702..48733217,2	K562	blood:
5	chr12:48691044..48692701-chr12:48738524..48740208,2	K562	blood:
6	chr12:48653420..48656308-chr12:48672282..48674655,2	K562	blood:
7	chr12:48702764..48705017-chr12:48706552..48708449,2	K562	blood:
8	chr12:48682061..48686479-chr12:48688143..48691883,6	K562	blood:
9	chr12:48689964..48692021-chr12:48694764..48697453,3	MCF-7	breast:
10	chr12:48695552..48697163-chr12:48743180..48744695,2	K562	blood:
11	chr12:48702764..48705017-chr12:48706552..48708449,2	K562	blood:
12	chr12:48699980..48702958-chr12:48704506..48706166,2	K562	blood:
13	chr12:48680562..48682797-chr12:48688715..48691085,2	MCF-7	breast:
14	chr12:48682061..48686479-chr12:48688143..48691883,6	K562	blood:
15	chr12:48591795..48593507-chr12:48675174..48677324,2	MCF-7	breast:
16	chr12:48690658..48693372-chr12:48744473..48746338,2	K562	blood:
17	chr12:48689964..48692021-chr12:48694764..48697453,3	MCF-7	breast:
18	chr12:48688262..48692290-chr12:48702214..48707293,5	K562	blood:
19	chr12:48679787..48682010-chr12:48684412..48686927,2	K562	blood:
20	chr12:48642199..48644196-chr12:48668410..48670451,2	K562	blood:
21	chr12:48680075..48681891-chr12:48683513..48685275,2	MCF-7	breast:
22	chr12:48683741..48686479-chr12:48688143..48689675,2	K562	blood:
23	chr12:48699980..48703428-chr12:48704506..48706488,3	K562	blood:
24	chr12:48700091..48702915-chr12:48742245..48744697,2	MCF-7	breast:
25	chr12:48691251..48692971-chr12:48699862..48702712,2	MCF-7	breast:
26	chr12:48672914..48675660-chr12:48743386..48744979,2	MCF-7	breast:
27	chr12:48699980..48702958-chr12:48704506..48706166,2	K562	blood:
28	chr12:48691251..48692971-chr12:48699862..48702712,2	MCF-7	breast:
29	chr12:48699980..48703428-chr12:48704506..48706488,3	K562	blood:
30	chr12:48677853..48680154-chr12:48686621..48688237,2	MCF-7	breast:
31	chr12:48695827..48697706-chr12:48743436..48745025,2	K562	blood:
32	chr12:48678386..48682435-chr12:48742177..48744865,4	MCF-7	breast:
33	chr12:48683741..48686479-chr12:48688143..48689675,2	K562	blood:
34	chr12:48652846..48655181-chr12:48658095..48660596,2	MCF-7	breast:
35	chr12:48689650..48692193-chr12:48742789..48745705,2	K562	blood:
36	chr12:48680562..48682797-chr12:48688715..48691085,2	MCF-7	breast:
37	chr12:48698712..48702509-chr12:48702715..48705745,3	MCF-7	breast:
38	chr12:48679787..48682010-chr12:48684412..48686927,2	K562	blood:
39	chr12:48680075..48681891-chr12:48683513..48685275,2	MCF-7	breast:
40	chr12:48688262..48692290-chr12:48702214..48707293,5	K562	blood:

No data

Variant related genes	Relation type
ENSG00000258234	TF binding region
ENSG00000258234	CpG island
ENSG00000258234	chromatin interactions
ENSG00000167528	chromatin interactions
ENSG00000269514	chromatin interactions
ENSG00000257735	chromatin interactions

Extended variants
information (count: 1368 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:1368 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs113619834	chr12:48658640-48658641	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs554857545	chr12:48658646-48658647	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs535773761	chr12:48658730-48658731	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs555681413	chr12:48658794-48658795	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs565943761	chr12:48658893-48658894	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs369385890	chr12:48658901-48658902	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs188353800	chr12:48658928-48658929	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs180722058	chr12:48658986-48658987	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs199846444	chr12:48659044-48659045	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs200017183	chr12:48659047-48659048	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs543142320	chr12:48659054-48659055	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs148386154	chr12:48659056-48659057	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs141565299	chr12:48659064-48659065	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs542778607	chr12:48659080-48659081	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs559642646	chr12:48659162-48659163	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs147100748	chr12:48659230-48659231	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs78077425	chr12:48659256-48659257	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs534160472	chr12:48659299-48659300	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs377658836	chr12:48659318-48659319	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs184791600	chr12:48659330-48659331	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs531082874	chr12:48659331-48659332	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs190033829	chr12:48659426-48659427	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs567979551	chr12:48659440-48659441	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs138470686	chr12:48659508-48659509	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs529113591	chr12:48659515-48659516	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs75421190	chr12:48659544-48659545	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs538195242	chr12:48659557-48659558	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs543504842	chr12:48659559-48659560	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs549168705	chr12:48659579-48659580	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs565981823	chr12:48659580-48659581	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs147366287	chr12:48659614-48659615	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs113291115	chr12:48659642-48659643	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs374100174	chr12:48659644-48659645	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs75036965	chr12:48659668-48659669	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs186005461	chr12:48659716-48659717	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs556796202	chr12:48659750-48659751	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs573374736	chr12:48659816-48659817	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs536452382	chr12:48659886-48659887	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs553112835	chr12:48659997-48659998	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs573243573	chr12:48660096-48660097	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs545377402	chr12:48660135-48660136	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs112083043	chr12:48660143-48660144	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs575531139	chr12:48660159-48660160	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs13377694	chr12:48660163-48660164	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs527581811	chr12:48660233-48660234	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs544558271	chr12:48660253-48660254	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs561387250	chr12:48660268-48660269	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs149466591	chr12:48660271-48660272	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs190415374	chr12:48660275-48660276	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs559577141	chr12:48660363-48660364	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:70)

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
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
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
Adenoid cystic carcinoma	18332873	CNVD
Breast cancer	21364760	CNVD
Prostate cancer	18632612	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
Bladder cancer	21909424	CNVD
Multiple myeloma	16616336	CNVD
Intracranial aneurysm	16715129	CNVD
Breast cancer	17661082	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21785460	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Intracranial ependymoma	16609018	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:390 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:48658600-48660800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr12:48659400-48659600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr12:48659600-48659800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
4	chr12:48659600-48659800	Enhancers	Primary B cells from peripheral blood	blood
5	chr12:48660200-48660600	Enhancers	Primary B cells from peripheral blood	blood
6	chr12:48669200-48669400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr12:48669400-48669600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr12:48669600-48675600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr12:48670400-48670600	Enhancers	Monocytes-CD14+_RO01746	blood
10	chr12:48670800-48672200	Weak transcription	Monocytes-CD14+_RO01746	blood
11	chr12:48672000-48681000	Enhancers	Primary monocytes fromperipheralblood	blood
12	chr12:48672200-48672400	Enhancers	Primary neutrophils fromperipheralblood	blood
13	chr12:48672200-48672800	Enhancers	Monocytes-CD14+_RO01746	blood
14	chr12:48672400-48672600	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
15	chr12:48672400-48673800	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
16	chr12:48672400-48674800	Enhancers	Placenta Amnion	Placenta Amnion
17	chr12:48672600-48674000	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
18	chr12:48672800-48673000	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
19	chr12:48672800-48673000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chr12:48672800-48673000	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
21	chr12:48672800-48673200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
22	chr12:48672800-48674200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
23	chr12:48673000-48673200	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
24	chr12:48673000-48673200	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
25	chr12:48673000-48673200	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
26	chr12:48673000-48673200	Bivalent Enhancer	iPS DF 6.9 Cell Line	embryonic stem cell
27	chr12:48673000-48674000	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
28	chr12:48673000-48674400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
29	chr12:48673200-48673400	Flanking Bivalent TSS/Enh	iPS-20b Cell Line	embryonic stem cell
30	chr12:48673200-48674000	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
31	chr12:48673200-48674000	Enhancers	Monocytes-CD14+_RO01746	blood
32	chr12:48673200-48674200	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
33	chr12:48673200-48674600	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
34	chr12:48673400-48674000	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
35	chr12:48673400-48674200	Enhancers	Brain Hippocampus Middle	brain
36	chr12:48673400-48676200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr12:48673600-48673800	Bivalent Enhancer	H9 Cell Line	embryonic stem cell
38	chr12:48673600-48673800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
39	chr12:48673800-48675000	Enhancers	Primary neutrophils fromperipheralblood	blood
40	chr12:48674000-48674200	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr12:48674000-48674200	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
42	chr12:48674000-48674600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
43	chr12:48674200-48674800	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
44	chr12:48674200-48680200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
45	chr12:48674400-48674800	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
46	chr12:48674600-48681000	Enhancers	Monocytes-CD14+_RO01746	blood
47	chr12:48674800-48675800	Weak transcription	Placenta Amnion	Placenta Amnion
48	chr12:48675000-48675400	Weak transcription	Primary neutrophils fromperipheralblood	blood
49	chr12:48675400-48676200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr12:48675400-48676400	Enhancers	Hela-S3	cervix

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