Variant report

Variant	nsv1013614
Chromosome Location	chr2:76624220-76715121
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:388)
CpG islands
(count:183)
Chromatin interactive
region (count:3)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:388 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr2:76664827-76665052	K562	blood:	n/a	n/a
2	ATF1	chr2:76642961-76643286	K562	blood:	n/a	n/a
3	ATF2	chr2:76642905-76643310	GM12878	blood:	n/a	n/a
4	ATF2	chr2:76642934-76643260	GM12878	blood:	n/a	n/a
5	ATF3	chr2:76664748-76664995	K562	blood:	n/a	n/a
6	BATF	chr2:76643007-76643384	GM12878	blood:	n/a	n/a
7	BATF	chr2:76672257-76672566	GM12878	blood:	n/a	n/a
8	BATF	chr2:76643008-76643306	GM12878	blood:	n/a	n/a
9	BATF	chr2:76677312-76677682	GM12878	blood:	n/a	chr2:76677532-76677543
10	BATF	chr2:76677367-76677642	GM12878	blood:	n/a	chr2:76677532-76677543
11	BCL11A	chr2:76677273-76677669	GM12878	blood:	n/a	chr2:76677532-76677541 chr2:76677531-76677540
12	BCL11A	chr2:76677294-76677677	GM12878	blood:	n/a	chr2:76677532-76677541 chr2:76677531-76677540
13	BCL11A	chr2:76672342-76672514	GM12878	blood:	n/a	n/a
14	BHLHE40	chr2:76674678-76674702	GM12878	blood:	n/a	n/a
15	BHLHE40	chr2:76677028-76677791	GM12878	blood:	n/a	n/a
16	BHLHE40	chr2:76672988-76673427	GM12878	blood:	n/a	n/a
17	BHLHE40	chr2:76649958-76650137	A549	lung:	n/a	n/a
18	BHLHE40	chr2:76643093-76643348	GM12878	blood:	n/a	n/a
19	CBX3	chr2:76672324-76672575	K562	blood:	n/a	n/a
20	CEBPB	chr2:76649651-76650021	A549	lung:	n/a	n/a
21	CEBPB	chr2:76639486-76639793	IMR90	lung:	n/a	n/a
22	CEBPB	chr2:76639457-76639746	K562	blood:	n/a	n/a
23	CEBPB	chr2:76664717-76665096	K562	blood:	n/a	chr2:76664885-76664896
24	CEBPB	chr2:76639471-76639814	HepG2	liver:	n/a	n/a
25	CEBPB	chr2:76639504-76639817	A549	lung:	n/a	n/a
26	CEBPB	chr2:76639550-76639796	H1-hESC	embryonic stem cell:	n/a	n/a
27	CEBPB	chr2:76634642-76634875	K562	blood:	n/a	chr2:76634741-76634752
28	CEBPB	chr2:76664751-76665017	HepG2	liver:	n/a	chr2:76664885-76664896
29	CEBPB	chr2:76648192-76648350	HepG2	liver:	n/a	chr2:76648248-76648259
30	CEBPB	chr2:76671535-76671853	HepG2	liver:	n/a	chr2:76671686-76671699
31	CEBPB	chr2:76681837-76682151	HepG2	liver:	n/a	chr2:76681975-76681986
32	CEBPB	chr2:76677879-76678560	HepG2	liver:	n/a	n/a
33	CEBPB	chr2:76681877-76682114	A549	lung:	n/a	chr2:76681975-76681986
34	CEBPB	chr2:76671548-76671857	A549	lung:	n/a	chr2:76671686-76671699
35	CEBPB	chr2:76634621-76634904	HepG2	liver:	n/a	chr2:76634741-76634752
36	CEBPB	chr2:76677893-76678050	A549	lung:	n/a	n/a
37	CHD1	chr2:76674597-76674742	GM12878	blood:	n/a	n/a
38	CHD1	chr2:76691539-76691643	GM12878	blood:	n/a	n/a
39	CHD2	chr2:76692627-76692630	H1-hESC	embryonic stem cell:	n/a	n/a
40	CHD2	chr2:76634762-76635104	K562	blood:	n/a	n/a
41	CHD2	chr2:76678041-76678047	GM12878	blood:	n/a	n/a
42	CHD2	chr2:76677097-76677691	GM12878	blood:	n/a	n/a
43	CHD2	chr2:76643049-76643381	GM12878	blood:	n/a	n/a
44	CHD2	chr2:76672988-76673329	GM12878	blood:	n/a	n/a
45	CTCF	chr2:76630940-76631090	GM12872	blood:	n/a	n/a
46	CTCF	chr2:76708540-76708690	Hela-S3	cervix:	n/a	n/a
47	CTCF	chr2:76691640-76691790	MCF-7	breast:	n/a	n/a
48	CTCF	chr2:76691520-76691670	Caco-2	colon:	n/a	chr2:76691617-76691638
49	CTCF	chr2:76691661-76691665	HepG2	liver:	n/a	n/a
50	CTCF	chr2:76691560-76691710	WERI-Rb-1	eye:	n/a	chr2:76691617-76691638

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:76672386-76672436	AG04449	skin:	fetal
2	chr2:76672386-76672436	HPAEpiC	pulmonary alveolar:	n/a
3	chr2:76672386-76672436	CMK	blood:	n/a
4	chr2:76674458-76674508	SKMC	muscle:	n/a
5	chr2:76705915-76705965	IMR90	lung:	fetal
6	chr2:76674458-76674508	PrEC	prostate:	n/a
7	chr2:76672386-76672436	Jurkat	blood:	n/a
8	chr2:76705915-76705965	PrEC	prostate:	n/a
9	chr2:76705915-76705965	AG04449	skin:	fetal
10	chr2:76674458-76674508	AG04450	lung:	fetal
11	chr2:76705915-76705965	HCM	heart:	n/a
12	chr2:76705915-76705965	PFSK-1	brain:	n/a
13	chr2:76674458-76674508	PFSK-1	brain:	n/a
14	chr2:76672386-76672436	MCF10A-Er-Src	breast:	n/a
15	chr2:76674458-76674508	HRPEpiC	eye:	n/a
16	chr2:76705915-76705965	K562	blood:	n/a
17	chr2:76705915-76705965	NHDF-neo	bronchial:	n/a
18	chr2:76674458-76674508	SK-N-SH_RA	brain:	n/a
19	chr2:76672386-76672436	BE2_C	brain:	n/a
20	chr2:76674458-76674508	SK-N-MC	brain:	n/a
21	chr2:76672386-76672436	HIPEpiC	eye:	n/a
22	chr2:76705915-76705965	HRPEpiC	eye:	n/a
23	chr2:76672386-76672436	HL-60	blood:	n/a
24	chr2:76705915-76705965	GM12892	blood:	n/a
25	chr2:76674458-76674508	HMEC	breast:	n/a
26	chr2:76705915-76705965	MCF-7	breast:	n/a
27	chr2:76672386-76672436	SK-N-SH	brain:	n/a
28	chr2:76672386-76672436	MCF-7	breast:	n/a
29	chr2:76674458-76674508	AG04449	skin:	fetal
30	chr2:76674458-76674508	GM19239	blood:	n/a
31	chr2:76705915-76705965	HPAEpiC	pulmonary alveolar:	n/a
32	chr2:76672386-76672436	NHBE	bronchial:	n/a
33	chr2:76705915-76705965	Hela-S3	cervix:	n/a
34	chr2:76672386-76672436	HCM	heart:	n/a
35	chr2:76705915-76705965	HCT-116	colon:	n/a
36	chr2:76674458-76674508	HPAEpiC	pulmonary alveolar:	n/a
37	chr2:76672386-76672436	HCPEpiC	choroid plexus:	n/a
38	chr2:76705915-76705965	GM06990	blood:	n/a
39	chr2:76674458-76674508	T-47D	breast:	n/a
40	chr2:76674458-76674508	K562	blood:	n/a
41	chr2:76672386-76672436	AG04450	lung:	fetal
42	chr2:76674458-76674508	BE2_C	brain:	n/a
43	chr2:76674458-76674508	BJ	skin:	n/a
44	chr2:76672386-76672436	K562	blood:	n/a
45	chr2:76674458-76674508	HRE	kidney:	n/a
46	chr2:76674458-76674508	NHBE	bronchial:	n/a
47	chr2:76674458-76674508	PANC-1	pancreas:	n/a
48	chr2:76674458-76674508	Caco-2	colon:	n/a
49	chr2:76672386-76672436	GM12891	blood:	n/a
50	chr2:76705915-76705965	NH-A	brain:	n/a

(count:3 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:76622373..76624695-chr2:76629073..76631639,2	K562	blood:
2	chr15:80860013..80860777-chr2:76680632..76681152,2	MCF-7	breast:
3	chr2:76622373..76624695-chr2:76629073..76631639,2	K562	blood:

No data

Variant related genes	Relation type
RN7SKP203	TF binding region
RN7SKP203	CpG island

Extended variants
information (count: 2312 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:2312 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17575455	chr2:76624220-76624221	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs112667268	chr2:76624231-76624232	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs73940411	chr2:76624268-76624269	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs571115034	chr2:76624323-76624324	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs548686597	chr2:76624338-76624339	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs139465959	chr2:76624340-76624341	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs375527790	chr2:76624357-76624358	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs181271619	chr2:76624382-76624383	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs186730161	chr2:76624510-76624511	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs74942231	chr2:76624517-76624518	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs191419776	chr2:76624550-76624551	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs540142114	chr2:76624594-76624595	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs116156741	chr2:76624610-76624611	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs573172222	chr2:76624632-76624633	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs181966511	chr2:76624661-76624662	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs561915582	chr2:76624690-76624691	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs112999148	chr2:76624699-76624700	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs544292990	chr2:76624702-76624703	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs368684889	chr2:76624707-76624708	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs186356204	chr2:76624720-76624721	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs115012749	chr2:76624765-76624766	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs544988886	chr2:76624916-76624917	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs147768332	chr2:76624923-76624924	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs527569637	chr2:76624941-76624942	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs549010006	chr2:76624946-76624947	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs191104533	chr2:76625014-76625015	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs376605031	chr2:76625028-76625029	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs549857258	chr2:76625032-76625033	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs13017817	chr2:76625060-76625061	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs539989017	chr2:76625094-76625095	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs10169401	chr2:76625113-76625114	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs528618138	chr2:76625160-76625161	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs548372528	chr2:76625167-76625168	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs534223517	chr2:76625246-76625247	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs368838025	chr2:76625247-76625248	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs77504030	chr2:76625324-76625325	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs372577733	chr2:76625344-76625345	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs183526460	chr2:76625407-76625408	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs544319683	chr2:76625436-76625437	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs556201657	chr2:76625445-76625446	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs186777746	chr2:76625503-76625504	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs191179644	chr2:76625572-76625573	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs370854004	chr2:76625589-76625590	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs560086110	chr2:76625671-76625672	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs527624590	chr2:76625674-76625675	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs139799610	chr2:76625681-76625682	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs369310599	chr2:76625720-76625721	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs73940412	chr2:76625738-76625739	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs182799441	chr2:76625826-76625827	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs145284061	chr2:76625858-76625859	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:57)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17387387	CNVD
Neuroblastoma	17533364	CNVD
Neuroblastoma	18923191	CNVD
Endometrial cancer	22040021	CNVD
Adrenal tumor	17535989	CNVD
Breast cancer	21264507	CNVD
Basal cell lymphoma	17053054	CNVD
Medulloblastoma	17522785	CNVD
Cancer	23418310	CNVD
Medulloblastoma	21979893	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Medulloblastoma	20607354	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Lung cancer	18438408	CNVD
Neurodevelopmental disorder	22521361	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Renal cell carcinoma	18765545	CNVD
Myxofibrosarcoma	16751306	CNVD
small cell lung cancer	20016488	CNVD
Acute myeloid leukemia	21251322	CNVD
Mental retardation	17124404	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Cancer	17440070	CNVD
Myelofibrosis	22110671	CNVD
Attention deficit hyperactivity disorder	21324949	CNVD
Breast cancer	16272173	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD

Chromatin state (count:96 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:76619200-76624400	Weak transcription	Duodenum Mucosa	Duodenum
2	chr2:76624200-76624400	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr2:76624200-76625400	Enhancers	Fetal Intestine Small	intestine
4	chr2:76624400-76624600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr2:76624400-76625000	Enhancers	Duodenum Mucosa	Duodenum
6	chr2:76624600-76625200	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr2:76624800-76625200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr2:76625200-76625400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr2:76625400-76627600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr2:76629200-76630400	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
11	chr2:76630000-76630600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
12	chr2:76631400-76633600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr2:76633400-76633600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
14	chr2:76633600-76634000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr2:76633600-76634000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr2:76640400-76640600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr2:76640800-76641400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
18	chr2:76641800-76643400	Enhancers	iPS-15b Cell Line	embryonic stem cell
19	chr2:76642200-76643400	Enhancers	H9 Cell Line	embryonic stem cell
20	chr2:76642400-76642600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
21	chr2:76642400-76643400	Enhancers	HUES6 Cell Line	embryonic stem cell
22	chr2:76643000-76643400	Enhancers	iPS-18 Cell Line	embryonic stem cell
23	chr2:76643400-76644200	Weak transcription	H9 Cell Line	embryonic stem cell
24	chr2:76644200-76644400	Enhancers	H9 Cell Line	embryonic stem cell
25	chr2:76648600-76649400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr2:76648800-76649200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr2:76654600-76657000	Enhancers	Hela-S3	cervix
28	chr2:76656200-76656800	Enhancers	Fetal Heart	heart
29	chr2:76656600-76656800	Enhancers	iPS-15b Cell Line	embryonic stem cell
30	chr2:76657200-76658400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
31	chr2:76657400-76657600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
32	chr2:76657600-76658800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
33	chr2:76658000-76659200	Enhancers	HUES48 Cell Line	embryonic stem cell
34	chr2:76658400-76658800	Enhancers	H9 Cell Line	embryonic stem cell
35	chr2:76658400-76659200	Enhancers	HUES64 Cell Line	embryonic stem cell
36	chr2:76658400-76659200	Enhancers	iPS-15b Cell Line	embryonic stem cell
37	chr2:76658600-76659200	Enhancers	iPS-18 Cell Line	embryonic stem cell
38	chr2:76658600-76659200	Enhancers	iPS-20b Cell Line	embryonic stem cell
39	chr2:76658800-76659200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
40	chr2:76658800-76659200	Enhancers	HUES6 Cell Line	embryonic stem cell
41	chr2:76658800-76659200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
42	chr2:76659000-76659400	Enhancers	ES-I3 Cell Line	embryonic stem cell
43	chr2:76659200-76677000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
44	chr2:76672400-76672800	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
45	chr2:76672800-76673800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
46	chr2:76673800-76674600	Enhancers	iPS-20b Cell Line	embryonic stem cell
47	chr2:76673800-76674800	Enhancers	iPS-18 Cell Line	embryonic stem cell
48	chr2:76674000-76674400	Enhancers	HUES64 Cell Line	embryonic stem cell
49	chr2:76674000-76674600	Enhancers	iPS-15b Cell Line	embryonic stem cell
50	chr2:76674000-76674800	Enhancers	HUES48 Cell Line	embryonic stem cell

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