Variant report

Variant	nsv899066
Chromosome Location	chr12:48667019-48713768
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:476)
CpG islands
(count:306)
Chromatin interactive
region (count:40)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:476 , 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	chr12:48690330-48690598	K562	blood:	n/a	n/a
2	ARID3A	chr12:48705888-48706088	K562	blood:	n/a	n/a
3	ARID3A	chr12:48697810-48697842	K562	blood:	n/a	n/a
4	ATF1	chr12:48705130-48705435	K562	blood:	n/a	n/a
5	ATF1	chr12:48690322-48690656	K562	blood:	n/a	n/a
6	ATF1	chr12:48675696-48675870	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	chr12:48670479-48670716	K562	blood:	n/a	n/a
12	CBX3	chr12:48690262-48690833	K562	blood:	n/a	n/a
13	CBX3	chr12:48670467-48670726	K562	blood:	n/a	n/a
14	CBX3	chr12:48705078-48705457	K562	blood:	n/a	n/a
15	CCNT2	chr12:48705180-48705450	K562	blood:	n/a	n/a
16	CCNT2	chr12:48690467-48690661	K562	blood:	n/a	n/a
17	CEBPB	chr12:48672987-48673226	MCF-7	breast:	n/a	n/a
18	CEBPB	chr12:48685858-48686172	K562	blood:	n/a	n/a
19	CEBPB	chr12:48685953-48686039	A549	lung:	n/a	n/a
20	CEBPB	chr12:48693069-48693135	K562	blood:	n/a	n/a
21	CEBPB	chr12:48676827-48676839	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr12:48691677-48691895	K562	blood:	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	chr12:48690440-48690590	HEEpiC	esophagus:	n/a	n/a
27	CTCF	chr12:48690420-48690570	AG04449	skin:	n/a	n/a
28	CTCF	chr12:48680580-48680730	GM12874	blood:	n/a	chr12:48680655-48680668
29	CTCF	chr12:48690400-48690550	HBMEC	blood vessel:	n/a	n/a
30	CTCF	chr12:48680560-48680710	HUVEC	blood vessel:	n/a	chr12:48680655-48680668
31	CTCF	chr12:48680551-48680735	GM10248	blood:	n/a	chr12:48680655-48680668
32	CTCF	chr12:48680640-48680790	GM12878	blood:	n/a	chr12:48680655-48680668
33	CTCF	chr12:48680540-48680690	AG09309	skin:	n/a	chr12:48680655-48680668
34	CTCF	chr12:48680600-48680750	GM12864	blood:	n/a	chr12:48680655-48680668
35	CTCF	chr12:48680973-48681054	GM13977	blood:	n/a	n/a
36	CTCF	chr12:48680540-48680690	HBMEC	blood vessel:	n/a	chr12:48680655-48680668
37	CTCF	chr12:48690360-48690510	HAc	cerebellar:	n/a	n/a
38	CTCF	chr12:48680500-48680650	NHEK	skin:	n/a	n/a
39	CTCF	chr12:48680620-48680770	HCFaa	heart:	n/a	chr12:48680655-48680668
40	CTCF	chr12:48680566-48680767	HUVEC	blood vessel:	n/a	chr12:48680655-48680668
41	CTCF	chr12:48680620-48680770	HCPEpiC	choroid plexus:	n/a	chr12:48680655-48680668
42	CTCF	chr12:48680541-48680798	A549	lung:	n/a	chr12:48680655-48680668
43	CTCF	chr12:48680512-48680781	K562	blood:	n/a	chr12:48680655-48680668
44	CTCF	chr12:48680560-48680710	RPTEC	kidney:	n/a	chr12:48680655-48680668
45	CTCF	chr12:48690482-48690577	Fibrobl	skin:	n/a	n/a
46	CTCF	chr12:48680501-48680797	K562	blood:	n/a	chr12:48680655-48680668
47	CTCF	chr12:48680600-48680750	AoAF	blood vessel:	n/a	chr12:48680655-48680668
48	CTCF	chr12:48680541-48680741	Spleen_OC	spleen:	n/a	chr12:48680655-48680668
49	CTCF	chr12:48690482-48690594	Pancreas_OC	pancreas:	n/a	n/a
50	CTCF	chr12:48680593-48680692	GM13976	blood:	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	chr12:48690974-48691024	BE2_C	brain:	n/a
2	chr12:48690974-48691024	BE2_C	brain:	n/a
3	chr12:48690546-48690596	Hela-S3	cervix:	n/a
4	chr12:48690915-48690965	GM12892	blood:	n/a
5	chr12:48690546-48690596	ECC-1	luminal epithelium:	n/a
6	chr12:48691036-48691086	HCT-116	colon:	n/a
7	chr12:48690546-48690596	NHBE	bronchial:	n/a
8	chr12:48690546-48690596	HPAEpiC	pulmonary alveolar:	n/a
9	chr12:48690974-48691024	NT2-D1	testis:	n/a
10	chr12:48690974-48691024	AG04449	skin:	fetal
11	chr12:48690689-48690739	HNPCEpiC	eye:	n/a
12	chr12:48691036-48691086	GM12878	blood:	n/a
13	chr12:48690974-48691024	Caco-2	colon:	n/a
14	chr12:48690689-48690739	AG04449	skin:	fetal
15	chr12:48690974-48691024	HPAEpiC	pulmonary alveolar:	n/a
16	chr12:48690689-48690739	HIPEpiC	eye:	n/a
17	chr12:48690915-48690965	HNPCEpiC	eye:	n/a
18	chr12:48690689-48690739	SK-N-MC	brain:	n/a
19	chr12:48691036-48691086	NHBE	bronchial:	n/a
20	chr12:48690546-48690596	AG04450	lung:	fetal
21	chr12:48690974-48691024	Hela-S3	cervix:	n/a
22	chr12:48691036-48691086	ECC-1	luminal epithelium:	n/a
23	chr12:48691036-48691086	HCM	heart:	n/a
24	chr12:48690915-48690965	AG09309	skin:	n/a
25	chr12:48690915-48690965	CMK	blood:	n/a
26	chr12:48690546-48690596	HepG2	liver:	n/a
27	chr12:48690546-48690596	RPTEC	kidney:	n/a
28	chr12:48690689-48690739	RPTEC	kidney:	n/a
29	chr12:48690546-48690596	Hepatocyte	liver:	n/a
30	chr12:48690915-48690965	BJ	skin:	n/a
31	chr12:48690546-48690596	HAEpiC	amniotic membrane:	n/a
32	chr12:48690689-48690739	SK-N-SH	brain:	n/a
33	chr12:48690546-48690596	ovcar-3	ovarian:	n/a
34	chr12:48690546-48690596	HCM	heart:	n/a
35	chr12:48691036-48691086	NH-A	brain:	n/a
36	chr12:48690689-48690739	HCF	heart:	n/a
37	chr12:48690915-48690965	HEK293	kidney:	embryo
38	chr12:48690546-48690596	AG09319	gingival:	n/a
39	chr12:48690974-48691024	K562	blood:	n/a
40	chr12:48690689-48690739	NHDF-neo	bronchial:	n/a
41	chr12:48690546-48690596	K562	blood:	n/a
42	chr12:48691036-48691086	PrEC	prostate:	n/a
43	chr12:48690915-48690965	RPTEC	kidney:	n/a
44	chr12:48690546-48690596	SK-N-SH	brain:	n/a
45	chr12:48691036-48691086	NT2-D1	testis:	n/a
46	chr12:48690689-48690739	ovcar-3	ovarian:	n/a
47	chr12:48690689-48690739	HPAEpiC	pulmonary alveolar:	n/a
48	chr12:48690974-48691024	HRCEpiC	kidney:	n/a
49	chr12:48691036-48691086	HNPCEpiC	eye:	n/a
50	chr12:48690546-48690596	PANC-1	pancreas:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr12:48680562..48682797-chr12:48688715..48691085,2	MCF-7	breast:
2	chr12:48699980..48703428-chr12:48704506..48706488,3	K562	blood:
3	chr12:48653420..48656308-chr12:48672282..48674655,2	K562	blood:
4	chr12:48642199..48644196-chr12:48668410..48670451,2	K562	blood:
5	chr12:48688262..48692290-chr12:48702214..48707293,5	K562	blood:
6	chr12:48689964..48692021-chr12:48694764..48697453,3	MCF-7	breast:
7	chr12:48699980..48702958-chr12:48704506..48706166,2	K562	blood:
8	chr12:48699980..48702958-chr12:48704506..48706166,2	K562	blood:
9	chr12:48680075..48681891-chr12:48683513..48685275,2	MCF-7	breast:
10	chr12:48695552..48697163-chr12:48743180..48744695,2	K562	blood:
11	chr12:48677853..48680154-chr12:48686621..48688237,2	MCF-7	breast:
12	chr12:48700091..48702915-chr12:48742245..48744697,2	MCF-7	breast:
13	chr12:48680562..48682797-chr12:48688715..48691085,2	MCF-7	breast:
14	chr12:48691251..48692971-chr12:48699862..48702712,2	MCF-7	breast:
15	chr12:48689964..48692021-chr12:48694764..48697453,3	MCF-7	breast:
16	chr12:48679787..48682010-chr12:48684412..48686927,2	K562	blood:
17	chr12:48678386..48682435-chr12:48742177..48744865,4	MCF-7	breast:
18	chr12:48591795..48593507-chr12:48675174..48677324,2	MCF-7	breast:
19	chr12:48698712..48702509-chr12:48702715..48705745,3	MCF-7	breast:
20	chr12:48689650..48692193-chr12:48742789..48745705,2	K562	blood:
21	chr12:48593487..48595723-chr12:48689162..48691231,3	K562	blood:
22	chr12:48691251..48692971-chr12:48699862..48702712,2	MCF-7	breast:
23	chr12:48682061..48686479-chr12:48688143..48691883,6	K562	blood:
24	chr12:48682061..48686479-chr12:48688143..48691883,6	K562	blood:
25	chr12:48712249..48713811-chr12:48741088..48742691,2	K562	blood:
26	chr12:48690658..48693372-chr12:48744473..48746338,2	K562	blood:
27	chr12:48688262..48692290-chr12:48702214..48707293,5	K562	blood:
28	chr12:48699980..48703428-chr12:48704506..48706488,3	K562	blood:
29	chr12:48704261..48706305-chr12:48731702..48733217,2	K562	blood:
30	chr12:48698712..48702509-chr12:48702715..48705745,3	MCF-7	breast:
31	chr12:48691044..48692701-chr12:48738524..48740208,2	K562	blood:
32	chr12:48695827..48697706-chr12:48743436..48745025,2	K562	blood:
33	chr12:48702764..48705017-chr12:48706552..48708449,2	K562	blood:
34	chr12:48679787..48682010-chr12:48684412..48686927,2	K562	blood:
35	chr12:48672914..48675660-chr12:48743386..48744979,2	MCF-7	breast:
36	chr12:48683741..48686479-chr12:48688143..48689675,2	K562	blood:
37	chr12:48680248..48681138-chr12:48730039..48730595,2	MCF-7	breast:
38	chr12:48683741..48686479-chr12:48688143..48689675,2	K562	blood:
39	chr12:48680075..48681891-chr12:48683513..48685275,2	MCF-7	breast:
40	chr12:48702764..48705017-chr12:48706552..48708449,2	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: 1304 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:1304 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs147666372	chr12:48669269-48669270	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs546922625	chr12:48669277-48669278	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs567035605	chr12:48669297-48669298	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs189892458	chr12:48669306-48669307	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs182464338	chr12:48669329-48669330	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs187036961	chr12:48669370-48669371	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs373337533	chr12:48669391-48669392	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs112690384	chr12:48669392-48669393	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs554963389	chr12:48669415-48669416	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs575028052	chr12:48669420-48669421	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs569772516	chr12:48669463-48669464	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs189501293	chr12:48669464-48669465	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs1906718	chr12:48669501-48669502	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
14	rs552685183	chr12:48669537-48669538	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs570531815	chr12:48669607-48669608	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs544846982	chr12:48669632-48669633	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs564838002	chr12:48669644-48669645	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs536305315	chr12:48669653-48669654	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs575153367	chr12:48669707-48669708	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs543844307	chr12:48669784-48669785	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs180689600	chr12:48669907-48669908	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs185309443	chr12:48669908-48669909	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs546661657	chr12:48669924-48669925	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs55649311	chr12:48669929-48669930	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs375544667	chr12:48669946-48669947	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs576511621	chr12:48669947-48669948	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs375070743	chr12:48669957-48669958	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs202167907	chr12:48669958-48669959	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs76994708	chr12:48669959-48669960	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs201274744	chr12:48669960-48669961	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs559960211	chr12:48669968-48669969	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs78481288	chr12:48669972-48669973	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs80068278	chr12:48669974-48669975	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs2932106	chr12:48670000-48670001	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
35	rs552760332	chr12:48670017-48670018	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs71453823	chr12:48670018-48670019	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs2932107	chr12:48670019-48670020	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
38	rs190418998	chr12:48670043-48670044	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs556987406	chr12:48670051-48670052	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs568421185	chr12:48670075-48670076	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs140278231	chr12:48670091-48670092	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs2956704	chr12:48670116-48670117	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
43	rs7304709	chr12:48670152-48670153	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
44	rs557872201	chr12:48670158-48670159	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs538835295	chr12:48670180-48670181	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs11168502	chr12:48670237-48670238	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs71439434	chr12:48670249-48670250	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs572690330	chr12:48670261-48670262	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs575191889	chr12:48670272-48670273	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs544077986	chr12:48670286-48670287	Weak transcription	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:385 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:48669200-48669400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr12:48669400-48669600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr12:48669600-48675600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr12:48670400-48670600	Enhancers	Monocytes-CD14+_RO01746	blood
5	chr12:48670800-48672200	Weak transcription	Monocytes-CD14+_RO01746	blood
6	chr12:48672000-48681000	Enhancers	Primary monocytes fromperipheralblood	blood
7	chr12:48672200-48672400	Enhancers	Primary neutrophils fromperipheralblood	blood
8	chr12:48672200-48672800	Enhancers	Monocytes-CD14+_RO01746	blood
9	chr12:48672400-48672600	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
10	chr12:48672400-48673800	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
11	chr12:48672400-48674800	Enhancers	Placenta Amnion	Placenta Amnion
12	chr12:48672600-48674000	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
13	chr12:48672800-48673000	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
14	chr12:48672800-48673000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr12:48672800-48673000	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
16	chr12:48672800-48673200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
17	chr12:48672800-48674200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
18	chr12:48673000-48673200	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
19	chr12:48673000-48673200	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
20	chr12:48673000-48673200	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
21	chr12:48673000-48673200	Bivalent Enhancer	iPS DF 6.9 Cell Line	embryonic stem cell
22	chr12:48673000-48674000	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
23	chr12:48673000-48674400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
24	chr12:48673200-48673400	Flanking Bivalent TSS/Enh	iPS-20b Cell Line	embryonic stem cell
25	chr12:48673200-48674000	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
26	chr12:48673200-48674000	Enhancers	Monocytes-CD14+_RO01746	blood
27	chr12:48673200-48674200	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
28	chr12:48673200-48674600	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
29	chr12:48673400-48674000	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
30	chr12:48673400-48674200	Enhancers	Brain Hippocampus Middle	brain
31	chr12:48673400-48676200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr12:48673600-48673800	Bivalent Enhancer	H9 Cell Line	embryonic stem cell
33	chr12:48673600-48673800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr12:48673800-48675000	Enhancers	Primary neutrophils fromperipheralblood	blood
35	chr12:48674000-48674200	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr12:48674000-48674200	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
37	chr12:48674000-48674600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
38	chr12:48674200-48674800	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
39	chr12:48674200-48680200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
40	chr12:48674400-48674800	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
41	chr12:48674600-48681000	Enhancers	Monocytes-CD14+_RO01746	blood
42	chr12:48674800-48675800	Weak transcription	Placenta Amnion	Placenta Amnion
43	chr12:48675000-48675400	Weak transcription	Primary neutrophils fromperipheralblood	blood
44	chr12:48675400-48676200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr12:48675400-48676400	Enhancers	Hela-S3	cervix
46	chr12:48675400-48676800	Enhancers	Primary neutrophils fromperipheralblood	blood
47	chr12:48675600-48675800	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
48	chr12:48675600-48676200	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
49	chr12:48675600-48676400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
50	chr12:48675800-48676200	Enhancers	Placenta Amnion	Placenta Amnion

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