Variant report

Variant	nsv1054215
Chromosome Location	chr12:73955467-74080646
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:222)
CpG islands
(count:61)
Chromatin interactive
region (count:6)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:222 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr12:74010248-74010400	K562	blood:	n/a	n/a
2	BACH1	chr12:74053673-74053952	H1-hESC	embryonic stem cell:	n/a	n/a
3	BHLHE40	chr12:73993330-73993343	GM12878	blood:	n/a	n/a
4	CEBPB	chr12:74021476-74021558	A549	lung:	n/a	n/a
5	CEBPB	chr12:74035798-74036052	A549	lung:	n/a	n/a
6	CEBPB	chr12:74022772-74023062	HepG2	liver:	n/a	chr12:74022915-74022926
7	CEBPB	chr12:74028234-74028479	HepG2	liver:	n/a	chr12:74028348-74028359
8	CEBPB	chr12:74028246-74028499	A549	lung:	n/a	chr12:74028348-74028359
9	CEBPB	chr12:74031940-74031970	A549	lung:	n/a	n/a
10	CEBPB	chr12:74021361-74021622	IMR90	lung:	n/a	n/a
11	CEBPB	chr12:74021381-74021691	H1-hESC	embryonic stem cell:	n/a	n/a
12	CHD2	chr12:73995941-73995952	H1-hESC	embryonic stem cell:	n/a	n/a
13	CTCF	chr12:74023740-74023890	HCT-116	colon:	n/a	n/a
14	CTCF	chr12:73959515-73959586	Lung_OC	lung:	n/a	n/a
15	CTCF	chr12:73966080-73966230	GM12869	blood:	n/a	n/a
16	CTCF	chr12:74050341-74050432	MCF-7	breast:	n/a	n/a
17	CTCF	chr12:74050139-74050519	MCF-7	breast:	n/a	n/a
18	CTCF	chr12:73961280-73961430	GM12866	blood:	n/a	n/a
19	CTCF	chr12:74050240-74050390	HEK293	kidney:	n/a	n/a
20	CTCF	chr12:74050296-74050452	Gliobla	brain:	n/a	n/a
21	CTCF	chr12:74023720-74023870	RPTEC	kidney:	n/a	n/a
22	CTCF	chr12:74023700-74023850	RPTEC	kidney:	n/a	n/a
23	CTCF	chr12:74023780-74023930	HEEpiC	esophagus:	n/a	n/a
24	CTCF	chr12:74050227-74050497	H1-hESC	embryonic stem cell:	n/a	n/a
25	CTCF	chr12:74050300-74050450	MCF-7	breast:	n/a	n/a
26	CTCF	chr12:74050293-74050485	MCF-7	breast:	n/a	n/a
27	CTCF	chr12:74023780-74023930	HMEC	breast:	n/a	n/a
28	CTCF	chr12:74050240-74050390	HCT-116	colon:	n/a	n/a
29	CTCF	chr12:74052511-74052528	HepG2	liver:	n/a	n/a
30	CTCF	chr12:74023740-74023890	HEEpiC	esophagus:	n/a	n/a
31	CTCF	chr12:74023740-74023890	HBMEC	blood vessel:	n/a	n/a
32	CTCF	chr12:74050280-74050430	MCF-7	breast:	n/a	n/a
33	CTCF	chr12:74050317-74050438	H1-hESC	embryonic stem cell:	n/a	n/a
34	CTCF	chr12:74023840-74023990	HCPEpiC	choroid plexus:	n/a	n/a
35	CTCF	chr12:74050340-74050490	HCT-116	colon:	n/a	n/a
36	CTCF	chr12:74050260-74050410	HBMEC	blood vessel:	n/a	n/a
37	CTCF	chr12:74050275-74050479	MCF-7	breast:	n/a	n/a
38	CTCF	chr12:73975268-73975304	Kidney_OC	kidney:	n/a	n/a
39	CTCF	chr12:74050372-74050402	Fibrobl	skin:	n/a	n/a
40	CTCF	chr12:74023820-74023970	HRPEpiC	eye:	n/a	n/a
41	CTCF	chr12:74050296-74050469	MCF-7	breast:	n/a	n/a
42	CTCF	chr12:74050260-74050410	SK-N-SH_RA	brain:	n/a	n/a
43	CTCF	chr12:74065480-74065553	Lung_OC	lung:	n/a	n/a
44	CTCF	chr12:74039140-74039290	GM12868	blood:	n/a	n/a
45	CTCF	chr12:74050329-74050430	MCF-7	breast:	n/a	n/a
46	E2F4	chr12:74033553-74033656	MCF10A-Er-Src	breast:	n/a	n/a
47	E2F4	chr12:74063708-74063822	MCF10A-Er-Src	breast:	n/a	n/a
48	EBF1	chr12:73973199-73973237	GM12878	blood:	n/a	n/a
49	EBF1	chr12:73983551-73983813	GM12878	blood:	n/a	chr12:73983698-73983708 chr12:73983698-73983707 chr12:73983696-73983709 chr12:73983697-73983708
50	EP300	chr12:74035261-74035344	GM12878	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:74072114-74072164	Jurkat	blood:	n/a
2	chr12:74072114-74072164	GM06990	blood:	n/a
3	chr12:74072114-74072164	Hepatocyte	liver:	n/a
4	chr12:74072114-74072164	GM12891	blood:	n/a
5	chr12:74072114-74072164	GM12878	blood:	n/a
6	chr12:74072114-74072164	HNPCEpiC	eye:	n/a
7	chr12:74072114-74072164	RPTEC	kidney:	n/a
8	chr12:74072114-74072164	GM12892	blood:	n/a
9	chr12:74072114-74072164	PrEC	prostate:	n/a
10	chr12:74072114-74072164	PFSK-1	brain:	n/a
11	chr12:74072114-74072164	MCF-7	breast:	n/a
12	chr12:74072114-74072164	Hela-S3	cervix:	n/a
13	chr12:74072114-74072164	AG09309	skin:	n/a
14	chr12:74072114-74072164	AG04449	skin:	fetal
15	chr12:74072114-74072164	BJ	skin:	n/a
16	chr12:74072114-74072164	ovcar-3	ovarian:	n/a
17	chr12:74072114-74072164	HPAEpiC	pulmonary alveolar:	n/a
18	chr12:74072114-74072164	HCF	heart:	n/a
19	chr12:74072114-74072164	T-47D	breast:	n/a
20	chr12:74072114-74072164	AoSMC	blood vessel:	n/a
21	chr12:74072114-74072164	HUVEC	blood vessel:	n/a
22	chr12:74072114-74072164	U87	brain:	n/a
23	chr12:74072114-74072164	NHDF-neo	bronchial:	n/a
24	chr12:74072114-74072164	Caco-2	colon:	n/a
25	chr12:74072114-74072164	ECC-1	luminal epithelium:	n/a
26	chr12:74072114-74072164	HCT-116	colon:	n/a
27	chr12:74072114-74072164	PANC-1	pancreas:	n/a
28	chr12:74072114-74072164	HEK293	kidney:	embryo
29	chr12:74072114-74072164	AG10803	skin:	n/a
30	chr12:74072114-74072164	SKMC	muscle:	n/a
31	chr12:74072114-74072164	NHBE	bronchial:	n/a
32	chr12:74072114-74072164	IMR90	lung:	fetal
33	chr12:74072114-74072164	HRE	kidney:	n/a
34	chr12:74072114-74072164	LNCaP	prostate:	n/a
35	chr12:74072114-74072164	HAEpiC	amniotic membrane:	n/a
36	chr12:74072114-74072164	AG09319	gingival:	n/a
37	chr12:74072114-74072164	HEEpiC	esophagus:	n/a
38	chr12:74072114-74072164	ProgFib	skin:	n/a
39	chr12:74072114-74072164	H1-hESC	embryonic stem cell:	embryo
40	chr12:74072114-74072164	HCM	heart:	n/a
41	chr12:74072114-74072164	NT2-D1	testis:	n/a
42	chr12:74072114-74072164	SK-N-SH_RA	brain:	n/a
43	chr12:74072114-74072164	BE2_C	brain:	n/a
44	chr12:74072114-74072164	SAEC	small airway:	n/a
45	chr12:74072114-74072164	HIPEpiC	eye:	n/a
46	chr12:74072114-74072164	A549	lung:	n/a
47	chr12:74072114-74072164	CMK	blood:	n/a
48	chr12:74072114-74072164	HRPEpiC	eye:	n/a
49	chr12:74072114-74072164	SK-N-MC	brain:	n/a
50	chr12:74072114-74072164	HepG2	liver:	n/a

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:74013871..74015768-chr12:74016739..74019231,2	MCF-7	breast:
2	chr12:74008618..74010272-chr12:74013442..74015238,2	K562	blood:
3	chr12:74035671..74038050-chr12:74931309..74933975,2	K562	blood:
4	chr12:74008618..74010272-chr12:74013442..74015238,2	K562	blood:
5	chr12:74013871..74015768-chr12:74016739..74019231,2	MCF-7	breast:
6	chr12:73908195..73908905-chr12:74049929..74050461,2	MCF-7	breast:

No data

Variant related genes	Relation type
RNU6-1012P	TF binding region
ENSG00000243164	TF binding region
RNU6-1012P	CpG island
ENSG00000243164	CpG island
ENSG00000253719	chromatin interactions
ENSG00000257386	chromatin interactions

Extended variants
information (count: 1990 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:1990 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs534783137	chr12:73965029-73965030	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs2363698	chr12:73965043-73965044	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
3	rs540155706	chr12:73965089-73965090	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs71458155	chr12:73965097-73965098	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs569143507	chr12:73965154-73965155	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs577223837	chr12:73965173-73965174	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs186349246	chr12:73965203-73965204	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs577945164	chr12:73965209-73965210	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs189484351	chr12:73965212-73965213	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs371387511	chr12:73965228-73965229	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs576563765	chr12:73965247-73965248	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs542349248	chr12:73965249-73965250	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs560735036	chr12:73965261-73965262	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs148456662	chr12:73965287-73965288	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs12309285	chr12:73965302-73965303	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs547757695	chr12:73965347-73965348	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs564404791	chr12:73965348-73965349	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs533467808	chr12:73965413-73965414	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs145268930	chr12:73965442-73965443	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs568522968	chr12:73965505-73965506	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs1443722	chr12:73965508-73965509	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs577890281	chr12:73965512-73965513	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs112809210	chr12:73965519-73965520	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs186740332	chr12:73965574-73965575	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs191989155	chr12:73965608-73965609	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs147612596	chr12:73965614-73965615	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs371675882	chr12:73965627-73965628	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs553703767	chr12:73965629-73965630	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs117005306	chr12:73965651-73965652	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs386376970	chr12:73965719-73965720	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs77922964	chr12:73965720-73965721	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs63417260	chr12:73965721-73965722	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs539751861	chr12:73965733-73965734	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs140646115	chr12:73965768-73965769	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs553421287	chr12:73965770-73965771	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs144487783	chr12:73965815-73965816	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs541936313	chr12:73965838-73965839	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs573164179	chr12:73965859-73965860	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs75533953	chr12:73965885-73965886	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs572464906	chr12:73965942-73965943	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs2028681	chr12:73965952-73965953	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs147775528	chr12:73965967-73965968	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs140050052	chr12:73965968-73965969	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs150324096	chr12:73965974-73965975	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs534206317	chr12:73991001-73991002	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs78133588	chr12:73991004-73991005	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs547074452	chr12:73991012-73991013	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs147752594	chr12:73991027-73991028	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs78553577	chr12:73991030-73991031	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs574847921	chr12:73991040-73991041	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:73)

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
Neurodevelopmental disorder	22521361	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
Colorectal cancer	16272173	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
Breast cancer	21785460	CNVD
Acute myeloid leukemia	21251322	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Burkitt''s lymphoma	20823134	CNVD
abnormal development	18461090	CNVD
Prostate cancer	18632612	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	16620391	CNVD
Disease	21505450	CNVD
craniofacial dysmorphism	21918468	CNVD
Breast cancer	21364760	CNVD
Breast cancer	17133270	CNVD
Urothelial cell carcinoma	18451213	CNVD
Myelofibrosis	22110671	CNVD
Cutaneous T-cell lymphoma	21881587	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
Hodgkin''s lymphoma	18641027	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Breast cancer	21509527	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:113 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:73965000-73966000	Enhancers	Muscle Satellite Cultured Cells	--
2	chr12:73991000-73991200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr12:73991200-73991400	Enhancers	HUES64 Cell Line	embryonic stem cell
4	chr12:73991200-73992000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr12:73991200-73994000	Enhancers	ES-I3 Cell Line	embryonic stem cell
6	chr12:73991400-73992000	Weak transcription	HUES64 Cell Line	embryonic stem cell
7	chr12:73991600-73991800	Enhancers	HUES48 Cell Line	embryonic stem cell
8	chr12:73991600-73993800	Enhancers	iPS-15b Cell Line	embryonic stem cell
9	chr12:73991800-73992800	Weak transcription	HUES48 Cell Line	embryonic stem cell
10	chr12:73992000-73992800	Enhancers	HUES64 Cell Line	embryonic stem cell
11	chr12:73992000-73993600	Enhancers	HUES6 Cell Line	embryonic stem cell
12	chr12:73992000-73994000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr12:73992000-73994200	Enhancers	iPS-20b Cell Line	embryonic stem cell
14	chr12:73992800-73993800	Enhancers	HUES48 Cell Line	embryonic stem cell
15	chr12:73993600-73999600	Weak transcription	HUES6 Cell Line	embryonic stem cell
16	chr12:73999600-73999800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr12:73999600-74000000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr12:73999600-74000000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr12:73999600-74000000	Enhancers	HUES48 Cell Line	embryonic stem cell
20	chr12:73999600-74000000	Enhancers	HUES6 Cell Line	embryonic stem cell
21	chr12:73999600-74000000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
22	chr12:73999600-74000000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr12:73999600-74000000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
24	chr12:74005800-74006800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr12:74006800-74007000	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr12:74007000-74009400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr12:74010400-74011400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr12:74010600-74011000	Enhancers	HUES48 Cell Line	embryonic stem cell
29	chr12:74011400-74017200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr12:74017200-74017600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr12:74017600-74018600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr12:74018600-74019000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr12:74019000-74020600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr12:74020600-74021000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr12:74022800-74023000	Enhancers	iPS-15b Cell Line	embryonic stem cell
36	chr12:74022800-74023200	Enhancers	H1 Cell Line	embryonic stem cell
37	chr12:74022800-74023200	Enhancers	H9 Cell Line	embryonic stem cell
38	chr12:74022800-74024000	Enhancers	iPS-18 Cell Line	embryonic stem cell
39	chr12:74023000-74023600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
40	chr12:74023000-74023800	Enhancers	iPS-20b Cell Line	embryonic stem cell
41	chr12:74023000-74024000	Enhancers	HUES48 Cell Line	embryonic stem cell
42	chr12:74023000-74024000	Enhancers	HUES6 Cell Line	embryonic stem cell
43	chr12:74023000-74024200	Enhancers	ES-I3 Cell Line	embryonic stem cell
44	chr12:74023200-74024000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
45	chr12:74023200-74024600	Enhancers	HUES64 Cell Line	embryonic stem cell
46	chr12:74023200-74025400	Weak transcription	H1 Cell Line	embryonic stem cell
47	chr12:74023600-74025600	Enhancers	iPS-15b Cell Line	embryonic stem cell
48	chr12:74023800-74024200	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
49	chr12:74024000-74024200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
50	chr12:74024000-74024400	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell

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