Variant report

Variant	nsv1007851
Chromosome Location	chr4:69667996-69713817
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:69683102-69684193	HepG2	liver:	n/a	chr4:69683103-69683119
2	ARID3A	chr4:69680934-69681903	HepG2	liver:	n/a	n/a
3	BHLHE40	chr4:69681403-69681779	HepG2	liver:	n/a	n/a
4	CBX3	chr4:69710563-69710928	K562	blood:	n/a	n/a
5	CEBPB	chr4:69685586-69685776	H1-hESC	embryonic stem cell:	n/a	chr4:69685612-69685625 chr4:69685612-69685625 chr4:69685612-69685625 chr4:69685613-69685624 chr4:69685612-69685623
6	CEBPB	chr4:69681686-69681867	HepG2	liver:	n/a	n/a
7	CEBPB	chr4:69685485-69685717	K562	blood:	n/a	chr4:69685612-69685625 chr4:69685612-69685625 chr4:69685612-69685625 chr4:69685613-69685624 chr4:69685612-69685623
8	CEBPB	chr4:69684063-69684187	K562	blood:	n/a	chr4:69684140-69684151 chr4:69684141-69684152
9	CEBPB	chr4:69681485-69681922	HepG2	liver:	n/a	n/a
10	CEBPB	chr4:69684002-69684205	A549	lung:	n/a	chr4:69684140-69684151 chr4:69684141-69684152
11	CEBPB	chr4:69684015-69684280	IMR90	lung:	n/a	chr4:69684140-69684151 chr4:69684141-69684152
12	CEBPB	chr4:69685492-69685778	IMR90	lung:	n/a	chr4:69685612-69685625 chr4:69685612-69685625 chr4:69685612-69685625 chr4:69685613-69685624 chr4:69685612-69685623
13	CEBPB	chr4:69685580-69685738	A549	lung:	n/a	chr4:69685612-69685625 chr4:69685612-69685625 chr4:69685612-69685625 chr4:69685613-69685624 chr4:69685612-69685623
14	CEBPB	chr4:69685477-69685793	HepG2	liver:	n/a	chr4:69685612-69685625 chr4:69685612-69685625 chr4:69685612-69685625 chr4:69685613-69685624 chr4:69685612-69685623
15	CEBPB	chr4:69712445-69712703	HepG2	liver:	n/a	chr4:69712549-69712560
16	CEBPB	chr4:69678841-69679067	HepG2	liver:	n/a	n/a
17	CEBPB	chr4:69683737-69684291	HepG2	liver:	n/a	chr4:69684140-69684151 chr4:69684141-69684152
18	CEBPD	chr4:69681639-69681887	HepG2	liver:	n/a	n/a
19	CTCF	chr4:69674820-69674970	GM12873	blood:	n/a	n/a
20	CTCF	chr4:69669990-69670027	Kidney_OC	kidney:	n/a	n/a
21	CTCF	chr4:69692957-69692997	Kidney_OC	kidney:	n/a	n/a
22	CTCF	chr4:69678039-69678143	Kidney_OC	kidney:	n/a	n/a
23	CTCF	chr4:69675017-69675085	Lung_OC	lung:	n/a	n/a
24	CTCF	chr4:69713220-69713370	GM12872	blood:	n/a	n/a
25	CTCF	chr4:69683829-69683943	Lung_OC	lung:	n/a	n/a
26	CTCF	chr4:69681974-69682009	Pancreas_OC	pancreas:	n/a	n/a
27	EP300	chr4:69681482-69681788	HepG2	liver:	n/a	chr4:69681630-69681640
28	EP300	chr4:69683551-69684101	HepG2	liver:	n/a	chr4:69683716-69683730 chr4:69683632-69683642
29	EP300	chr4:69681227-69681937	HepG2	liver:	n/a	chr4:69681630-69681640
30	EP300	chr4:69681124-69681935	A549	lung:	n/a	chr4:69681630-69681640
31	EP300	chr4:69683119-69683383	HepG2	liver:	n/a	n/a
32	EP300	chr4:69683627-69684145	HepG2	liver:	n/a	chr4:69683716-69683730 chr4:69683632-69683642
33	EP300	chr4:69705426-69705448	K562	blood:	n/a	n/a
34	EP300	chr4:69681270-69682024	HepG2	liver:	n/a	chr4:69681630-69681640
35	EP300	chr4:69683110-69683464	HepG2	liver:	n/a	chr4:69683437-69683451
36	EP300	chr4:69681295-69681781	A549	lung:	n/a	chr4:69681630-69681640
37	FOSL2	chr4:69687855-69688221	HepG2	liver:	n/a	n/a
38	FOSL2	chr4:69683671-69684057	HepG2	liver:	n/a	chr4:69683978-69683990
39	FOSL2	chr4:69683663-69683966	HepG2	liver:	n/a	n/a
40	FOSL2	chr4:69681428-69682033	HepG2	liver:	n/a	n/a
41	FOSL2	chr4:69681366-69682455	HepG2	liver:	n/a	n/a
42	FOSL2	chr4:69682047-69682360	HepG2	liver:	n/a	n/a
43	FOSL2	chr4:69693621-69693993	A549	lung:	n/a	n/a
44	FOSL2	chr4:69687920-69688219	HepG2	liver:	n/a	n/a
45	FOXA1	chr4:69683674-69684035	HepG2	liver:	n/a	n/a
46	FOXA1	chr4:69682696-69684401	HepG2	liver:	n/a	n/a
47	FOXA1	chr4:69683614-69684060	HepG2	liver:	n/a	n/a
48	FOXA1	chr4:69681268-69681979	HepG2	liver:	n/a	chr4:69681561-69681576
49	FOXA1	chr4:69687653-69688234	HepG2	liver:	n/a	n/a
50	FOXA1	chr4:69683068-69684396	HepG2	liver:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:69681824-69681874	ovcar-3	ovarian:	n/a
2	chr4:69681824-69681874	HUVEC	blood vessel:	n/a
3	chr4:69681824-69681874	HNPCEpiC	eye:	n/a
4	chr4:69681824-69681874	HCF	heart:	n/a
5	chr4:69681824-69681874	HPAEpiC	pulmonary alveolar:	n/a
6	chr4:69681824-69681874	HIPEpiC	eye:	n/a
7	chr4:69681824-69681874	CMK	blood:	n/a
8	chr4:69681824-69681874	H1-hESC	embryonic stem cell:	embryo
9	chr4:69681824-69681874	HRE	kidney:	n/a
10	chr4:69681824-69681874	HCT-116	colon:	n/a
11	chr4:69681824-69681874	HCM	heart:	n/a
12	chr4:69681824-69681874	HAEpiC	amniotic membrane:	n/a
13	chr4:69681824-69681874	GM12878	blood:	n/a
14	chr4:69681824-69681874	GM19239	blood:	n/a
15	chr4:69681824-69681874	T-47D	breast:	n/a
16	chr4:69681824-69681874	SK-N-SH	brain:	n/a
17	chr4:69681824-69681874	SAEC	small airway:	n/a
18	chr4:69681824-69681874	NHDF-neo	bronchial:	n/a
19	chr4:69681824-69681874	Hepatocyte	liver:	n/a
20	chr4:69681824-69681874	NH-A	brain:	n/a
21	chr4:69681824-69681874	Hela-S3	cervix:	n/a
22	chr4:69681824-69681874	AG09309	skin:	n/a
23	chr4:69681824-69681874	SKMC	muscle:	n/a
24	chr4:69681824-69681874	IMR90	lung:	fetal
25	chr4:69681824-69681874	K562	blood:	n/a
26	chr4:69681824-69681874	HRPEpiC	eye:	n/a
27	chr4:69681824-69681874	RPTEC	kidney:	n/a
28	chr4:69681824-69681874	NB4	blood:	n/a
29	chr4:69681824-69681874	NHBE	bronchial:	n/a
30	chr4:69681824-69681874	ProgFib	skin:	n/a
31	chr4:69681824-69681874	HMEC	breast:	n/a
32	chr4:69681824-69681874	Caco-2	colon:	n/a
33	chr4:69681824-69681874	U87	brain:	n/a
34	chr4:69681824-69681874	Jurkat	blood:	n/a
35	chr4:69681824-69681874	GM12892	blood:	n/a
36	chr4:69681824-69681874	NT2-D1	testis:	n/a
37	chr4:69681824-69681874	HCPEpiC	choroid plexus:	n/a
38	chr4:69681824-69681874	AoSMC	blood vessel:	n/a
39	chr4:69681824-69681874	PANC-1	pancreas:	n/a
40	chr4:69681824-69681874	LNCaP	prostate:	n/a
41	chr4:69681824-69681874	HepG2	liver:	n/a
42	chr4:69681824-69681874	GM12891	blood:	n/a
43	chr4:69681824-69681874	ECC-1	luminal epithelium:	n/a
44	chr4:69681824-69681874	AG09319	gingival:	n/a
45	chr4:69681824-69681874	BJ	skin:	n/a
46	chr4:69681824-69681874	AG04449	skin:	fetal
47	chr4:69681824-69681874	BE2_C	brain:	n/a
48	chr4:69681824-69681874	HEEpiC	esophagus:	n/a
49	chr4:69681824-69681874	SK-N-MC	brain:	n/a
50	chr4:69681824-69681874	PrEC	prostate:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr4:69673177..69674687-chr4:70085938..70087696,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-UGT2B10-1	chr4:69679713-69680445	NONHSAT096742

Variant related genes	Relation type
ENSG00000251236	TF binding region
UGT2B10	TF binding region
ENSG00000251424	TF binding region
ENSG00000251236	CpG island
UGT2B10	CpG island
ENSG00000251424	CpG island

Extended variants
information (count: 1926 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:1926 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs537594995	chr4:69668406-69668407	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs551304027	chr4:69668433-69668434	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs571201788	chr4:69668492-69668493	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs185583663	chr4:69668504-69668505	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs553430191	chr4:69668505-69668506	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs573136975	chr4:69668507-69668508	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs73823942	chr4:69668510-69668511	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs112092622	chr4:69668520-69668521	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs72849009	chr4:69668587-69668588	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs190449124	chr4:69668597-69668598	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs145091166	chr4:69668602-69668603	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs577562951	chr4:69668614-69668615	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs183036797	chr4:69668654-69668655	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs560130388	chr4:69668656-69668657	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs528849783	chr4:69668668-69668669	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs373657739	chr4:69668674-69668675	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs542709513	chr4:69668679-69668680	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs562402451	chr4:69668704-69668705	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs73823943	chr4:69668714-69668715	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs113570506	chr4:69668726-69668727	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs112816466	chr4:69668736-69668737	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs571032820	chr4:69668795-69668796	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs368664728	chr4:69668876-69668877	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs371671581	chr4:69668909-69668910	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs188770715	chr4:69668926-69668927	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs546941310	chr4:69668940-69668941	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs566878261	chr4:69668979-69668980	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs193258393	chr4:69668984-69668985	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs555841612	chr4:69668986-69668987	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs569053539	chr4:69668990-69668991	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs114805626	chr4:69669051-69669052	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs115686602	chr4:69669052-69669053	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs577400614	chr4:69669064-69669065	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs540153973	chr4:69669068-69669069	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs114081568	chr4:69669095-69669096	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs573590668	chr4:69669119-69669120	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs542298684	chr4:69669130-69669131	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs10028844	chr4:69669134-69669135	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs10000284	chr4:69669183-69669184	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs575555024	chr4:69669197-69669198	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs149026211	chr4:69669201-69669202	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs10028938	chr4:69669216-69669217	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs118153392	chr4:69669235-69669236	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs112566859	chr4:69669268-69669269	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs377293303	chr4:69669269-69669270	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs9993124	chr4:69669270-69669271	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs140380019	chr4:69669271-69669272	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs113957126	chr4:69669276-69669277	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs114298414	chr4:69669281-69669282	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs10000400	chr4:69669309-69669310	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:84)

Disease	PMID	Source
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Lung cancer	18438408	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	21922591	CNVD
Parkinson disease	21956041	CNVD
Mental retardation	20522426	CNVD
delayed speech	20522426	CNVD
growth disorder	20522426	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Parkinson disease	18923514	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Breast cancer	16272173	CNVD
Multiple myeloma	16616336	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Oral squamous cell carcinoma	17134496	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Colorectal cancer	16272173	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Osteoporosis	18992858	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelodysplastic syndrome	21251322	CNVD
Multiple myeloma	17550852	CNVD
Graft versus host disease	20877625	CNVD
Breast cancer	21990379	CNVD
Myelofibrosis	22110671	CNVD
Osteoporosis	20877625	CNVD
Osteoporosis	19737800	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Glioblastoma multiforme	21138945	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Oral cancer	21386901	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
small cell lung cancer	20016488	CNVD
early-passage human iPS cells	21368824	CNVD
Pancreatic cancer	17952125	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:76 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:69668400-69670000	Enhancers	Fetal Intestine Small	intestine
2	chr4:69669400-69673000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr4:69670400-69671000	Enhancers	iPS-18 Cell Line	embryonic stem cell
4	chr4:69670600-69671200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
5	chr4:69671000-69671200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr4:69671200-69673000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
7	chr4:69673000-69673600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
8	chr4:69673600-69674000	Enhancers	Liver	Liver
9	chr4:69676600-69678000	Enhancers	HepG2	liver
10	chr4:69678000-69678400	Weak transcription	HepG2	liver
11	chr4:69678400-69679200	Enhancers	HepG2	liver
12	chr4:69679200-69679600	Weak transcription	HepG2	liver
13	chr4:69679600-69681800	Enhancers	HepG2	liver
14	chr4:69680800-69681200	Enhancers	Liver	Liver
15	chr4:69681000-69682600	Enhancers	A549	lung
16	chr4:69681200-69681800	Weak transcription	Liver	Liver
17	chr4:69681400-69682000	Enhancers	iPS-18 Cell Line	embryonic stem cell
18	chr4:69681600-69684000	Enhancers	HUES48 Cell Line	embryonic stem cell
19	chr4:69681800-69682200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr4:69681800-69682600	Enhancers	HUES6 Cell Line	embryonic stem cell
21	chr4:69681800-69682600	Enhancers	iPS-15b Cell Line	embryonic stem cell
22	chr4:69681800-69683000	Enhancers	HUES64 Cell Line	embryonic stem cell
23	chr4:69681800-69683000	Flanking Active TSS	HepG2	liver
24	chr4:69681800-69684600	Active TSS	Liver	Liver
25	chr4:69682000-69682200	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
26	chr4:69682200-69682400	Enhancers	iPS-18 Cell Line	embryonic stem cell
27	chr4:69682200-69682800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr4:69682400-69682600	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
29	chr4:69682400-69682800	Enhancers	iPS-20b Cell Line	embryonic stem cell
30	chr4:69682400-69682800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
31	chr4:69682600-69683200	Enhancers	iPS-18 Cell Line	embryonic stem cell
32	chr4:69682600-69683600	Weak transcription	HUES6 Cell Line	embryonic stem cell
33	chr4:69682600-69683600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
34	chr4:69682600-69683800	Weak transcription	A549	lung
35	chr4:69682800-69684200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
36	chr4:69683000-69683400	Weak transcription	HUES64 Cell Line	embryonic stem cell
37	chr4:69683000-69683600	Active TSS	HepG2	liver
38	chr4:69683200-69683600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
39	chr4:69683400-69684800	Enhancers	HUES64 Cell Line	embryonic stem cell
40	chr4:69683600-69683800	Flanking Active TSS	HepG2	liver
41	chr4:69683600-69684200	Enhancers	iPS-15b Cell Line	embryonic stem cell
42	chr4:69683600-69684200	Enhancers	iPS-18 Cell Line	embryonic stem cell
43	chr4:69683800-69684000	Enhancers	HUES6 Cell Line	embryonic stem cell
44	chr4:69683800-69684000	Enhancers	A549	lung
45	chr4:69683800-69684000	Active TSS	HepG2	liver
46	chr4:69684000-69684200	Flanking Active TSS	HepG2	liver
47	chr4:69684200-69684600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
48	chr4:69684200-69686000	Enhancers	HepG2	liver
49	chr4:69684600-69686000	Flanking Active TSS	Liver	Liver
50	chr4:69686000-69686600	Enhancers	Liver	Liver

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