Variant report

Variant	nsv980214
Chromosome Location	chr4:70039464-70084276
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:187)
CpG islands
(count:244)
Chromatin interactive
region (count:2)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:187 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:70047409-70047599	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:70056442-70056604	HepG2	liver:	n/a	n/a
3	ARID3A	chr4:70080605-70080753	HepG2	liver:	n/a	n/a
4	ARID3A	chr4:70045525-70045926	HepG2	liver:	n/a	n/a
5	ATF1	chr4:70044510-70044858	K562	blood:	n/a	n/a
6	BCL3	chr4:70080358-70080837	A549	lung:	n/a	n/a
7	BHLHE40	chr4:70057696-70057810	K562	blood:	n/a	n/a
8	BHLHE40	chr4:70044628-70044869	K562	blood:	n/a	n/a
9	BHLHE40	chr4:70047447-70047661	HepG2	liver:	n/a	n/a
10	CEBPB	chr4:70045638-70045779	HepG2	liver:	n/a	n/a
11	CEBPB	chr4:70047441-70047516	HepG2	liver:	n/a	n/a
12	CEBPB	chr4:70046596-70046924	HepG2	liver:	n/a	chr4:70046754-70046765 chr4:70046753-70046764
13	CEBPB	chr4:70077980-70078075	K562	blood:	n/a	chr4:70078030-70078041 chr4:70078032-70078043
14	CEBPB	chr4:70077864-70078215	IMR90	lung:	n/a	chr4:70078030-70078041 chr4:70078032-70078043
15	CEBPB	chr4:70077881-70078188	HepG2	liver:	n/a	chr4:70078030-70078041 chr4:70078032-70078043
16	CEBPB	chr4:70044569-70044904	K562	blood:	n/a	n/a
17	CEBPB	chr4:70044638-70044861	K562	blood:	n/a	n/a
18	CEBPB	chr4:70045536-70045885	HepG2	liver:	n/a	n/a
19	CEBPB	chr4:70080509-70080873	A549	lung:	n/a	n/a
20	CEBPB	chr4:70059993-70060205	HepG2	liver:	n/a	n/a
21	CEBPD	chr4:70044512-70044940	K562	blood:	n/a	n/a
22	CEBPD	chr4:70045604-70045791	HepG2	liver:	n/a	n/a
23	CREB1	chr4:70045635-70045816	HepG2	liver:	n/a	n/a
24	CTCF	chr4:70077161-70077220	Kidney_OC	kidney:	n/a	n/a
25	CTCF	chr4:70071636-70071728	GM13977	blood:	n/a	n/a
26	CTCF	chr4:70081934-70082033	GM10248	blood:	n/a	n/a
27	CTCF	chr4:70070599-70070664	Kidney_OC	kidney:	n/a	n/a
28	CTCF	chr4:70082912-70082994	GM10248	blood:	n/a	n/a
29	CTCF	chr4:70078196-70078250	GM13976	blood:	n/a	n/a
30	CTCF	chr4:70057643-70057792	Lung_OC	lung:	n/a	n/a
31	CTCF	chr4:70047877-70047968	GM20000	blood:	n/a	n/a
32	EP300	chr4:70057617-70057880	HepG2	liver:	n/a	n/a
33	EP300	chr4:70057612-70057966	HepG2	liver:	n/a	n/a
34	EP300	chr4:70047299-70047624	HepG2	liver:	n/a	n/a
35	EP300	chr4:70045506-70045892	HepG2	liver:	n/a	n/a
36	EP300	chr4:70044528-70044879	K562	blood:	n/a	n/a
37	EP300	chr4:70057617-70057828	K562	blood:	n/a	n/a
38	EP300	chr4:70080278-70081011	A549	lung:	n/a	n/a
39	EP300	chr4:70080436-70080904	A549	lung:	n/a	n/a
40	EP300	chr4:70045534-70045853	HepG2	liver:	n/a	n/a
41	FOS	chr4:70062387-70062626	MCF10A-Er-Src	breast:	n/a	n/a
42	FOS	chr4:70062305-70062621	MCF10A-Er-Src	breast:	n/a	n/a
43	FOS	chr4:70062379-70062485	MCF10A-Er-Src	breast:	n/a	n/a
44	FOSL2	chr4:70080058-70080390	HepG2	liver:	n/a	n/a
45	FOSL2	chr4:70080425-70080929	A549	lung:	n/a	n/a
46	FOSL2	chr4:70044601-70044826	HepG2	liver:	n/a	n/a
47	FOSL2	chr4:70045493-70045940	HepG2	liver:	n/a	chr4:70045732-70045743
48	FOSL2	chr4:70047280-70047975	HepG2	liver:	n/a	n/a
49	FOSL2	chr4:70047294-70047641	HepG2	liver:	n/a	n/a
50	FOSL2	chr4:70045509-70046001	HepG2	liver:	n/a	chr4:70045732-70045743

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:70065325-70065375	HCF	heart:	n/a
2	chr4:70080453-70080503	NHDF-neo	bronchial:	n/a
3	chr4:70080453-70080503	NH-A	brain:	n/a
4	chr4:70065325-70065375	PrEC	prostate:	n/a
5	chr4:70065325-70065375	RPTEC	kidney:	n/a
6	chr4:70066318-70066368	A549	lung:	n/a
7	chr4:70065325-70065375	HEEpiC	esophagus:	n/a
8	chr4:70064835-70064885	SK-N-SH_RA	brain:	n/a
9	chr4:70080453-70080503	NB4	blood:	n/a
10	chr4:70066318-70066368	SKMC	muscle:	n/a
11	chr4:70064835-70064885	GM19239	blood:	n/a
12	chr4:70065325-70065375	HCPEpiC	choroid plexus:	n/a
13	chr4:70065325-70065375	AG09319	gingival:	n/a
14	chr4:70065325-70065375	HIPEpiC	eye:	n/a
15	chr4:70080453-70080503	PANC-1	pancreas:	n/a
16	chr4:70065325-70065375	GM12891	blood:	n/a
17	chr4:70066318-70066368	PFSK-1	brain:	n/a
18	chr4:70065325-70065375	HCM	heart:	n/a
19	chr4:70064835-70064885	PFSK-1	brain:	n/a
20	chr4:70080453-70080503	HepG2	liver:	n/a
21	chr4:70080453-70080503	NHBE	bronchial:	n/a
22	chr4:70066318-70066368	SK-N-MC	brain:	n/a
23	chr4:70064835-70064885	AG10803	skin:	n/a
24	chr4:70064835-70064885	RPTEC	kidney:	n/a
25	chr4:70066318-70066368	HL-60	blood:	n/a
26	chr4:70065325-70065375	Caco-2	colon:	n/a
27	chr4:70065325-70065375	HMEC	breast:	n/a
28	chr4:70080453-70080503	H1-hESC	embryonic stem cell:	embryo
29	chr4:70080453-70080503	HRCEpiC	kidney:	n/a
30	chr4:70080453-70080503	Hepatocyte	liver:	n/a
31	chr4:70066318-70066368	AG09319	gingival:	n/a
32	chr4:70065325-70065375	HL-60	blood:	n/a
33	chr4:70065325-70065375	NB4	blood:	n/a
34	chr4:70066318-70066368	ovcar-3	ovarian:	n/a
35	chr4:70080453-70080503	ECC-1	luminal epithelium:	n/a
36	chr4:70065325-70065375	Hela-S3	cervix:	n/a
37	chr4:70080453-70080503	AG04450	lung:	fetal
38	chr4:70066318-70066368	Hepatocyte	liver:	n/a
39	chr4:70080453-70080503	MCF10A-Er-Src	breast:	n/a
40	chr4:70080453-70080503	HEEpiC	esophagus:	n/a
41	chr4:70065325-70065375	H1-hESC	embryonic stem cell:	embryo
42	chr4:70080453-70080503	HRPEpiC	eye:	n/a
43	chr4:70080453-70080503	SAEC	small airway:	n/a
44	chr4:70064835-70064885	Hela-S3	cervix:	n/a
45	chr4:70065325-70065375	HPAEpiC	pulmonary alveolar:	n/a
46	chr4:70064835-70064885	AoSMC	blood vessel:	n/a
47	chr4:70066318-70066368	HEEpiC	esophagus:	n/a
48	chr4:70065325-70065375	AoSMC	blood vessel:	n/a
49	chr4:70065325-70065375	IMR90	lung:	fetal
50	chr4:70064835-70064885	AG04450	lung:	fetal

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr4:70060045..70062674-chr4:70067007..70069842,2	MCF-7	breast:
2	chr4:70060045..70062674-chr4:70067007..70069842,2	MCF-7	breast:

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-UGT2B28-1	chr4:70066190-70066296	ENSG00000250696.1
2	lnc-UGT2B28-1	chr4:70047378-70048090	NONHSAT096756
3	lnc-UGT2B28-1	chr4:70080191-70080193	ENSG00000250696.1
4	lnc-UGT2B28-1	chr4:70080191-70082484	ENSG00000250696.1
5	lnc-UGT2B28-1	chr4:70047818-70048090	ENSG00000250696.1
6	lnc-UGT2B28-1	chr4:70066890-70067002	ENSG00000250696.1
7	lnc-UGT2B28-1	chr4:70076784-70076865	ENSG00000250696.1
8	lnc-UGT2B28-1	chr4:70066138-70066296	ENSG00000250696.1
9	lnc-UGT2B28-1	chr4:70076784-70076865	ENSG00000250696.1
10	lnc-UGT2B28-1	chr4:70061386-70061489	ENSG00000250696.1

No data

Variant related genes	Relation type
ENSG00000196472	TF binding region
ENSG00000250696	TF binding region
ENSG00000268803	TF binding region
UGT2B11	TF binding region
ENSG00000196472	CpG island
ENSG00000250696	CpG island
ENSG00000268803	CpG island
UGT2B11	CpG island

Extended variants
information (count: 1544 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:1544 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs572838666	chr4:70039495-70039496	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs535253049	chr4:70039524-70039525	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs555186266	chr4:70039525-70039526	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs575238090	chr4:70039527-70039528	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs544302438	chr4:70039561-70039562	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs78584760	chr4:70039575-70039576	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs577586496	chr4:70039587-70039588	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs187190767	chr4:70039597-70039598	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs140920630	chr4:70039600-70039601	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs560072316	chr4:70039610-70039611	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs57718545	chr4:70039640-70039641	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs376120489	chr4:70039643-70039644	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs575319220	chr4:70039657-70039658	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs548791077	chr4:70039695-70039696	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs562317658	chr4:70039696-70039697	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs543939469	chr4:70039709-70039710	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs79215887	chr4:70039712-70039713	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs570724938	chr4:70039755-70039756	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs369098836	chr4:70039784-70039785	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs72126418	chr4:70039785-70039786	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs200148532	chr4:70039788-70039789	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs58159026	chr4:70039790-70039791	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs201353376	chr4:70039819-70039820	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs574049413	chr4:70039824-70039825	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs546619391	chr4:70039831-70039832	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs34798480	chr4:70039861-70039862	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs397880472	chr4:70039867-70039868	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs566429169	chr4:70039871-70039872	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs34286575	chr4:70039901-70039902	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs199893247	chr4:70039904-70039905	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs201046013	chr4:70039905-70039906	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs35823180	chr4:70039908-70039909	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs540184253	chr4:70039929-70039930	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs575397545	chr4:70039945-70039946	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs192004426	chr4:70039949-70039950	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs55862101	chr4:70039976-70039977	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs373392629	chr4:70039977-70039978	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs75626389	chr4:70040003-70040004	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs577697798	chr4:70040015-70040016	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs370143935	chr4:70040019-70040020	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs66814768	chr4:70040043-70040044	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs185459897	chr4:70040045-70040046	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs573537971	chr4:70040051-70040052	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs542543944	chr4:70040062-70040063	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs116138788	chr4:70040065-70040066	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs140438297	chr4:70040067-70040068	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs562506717	chr4:70040077-70040078	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs34898320	chr4:70040093-70040094	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs544515107	chr4:70040110-70040111	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs564585040	chr4:70040175-70040176	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:83)

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
Non-syndromic sensorineural hearing loss	17122850	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Schizophrenia	21346763	CNVD

Chromatin state (count:57 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:70035200-70043600	Weak transcription	Fetal Intestine Small	intestine
2	chr4:70038800-70041000	Weak transcription	Liver	Liver
3	chr4:70041000-70042000	Strong transcription	Liver	Liver
4	chr4:70042000-70044400	Weak transcription	Liver	Liver
5	chr4:70043600-70043800	Enhancers	Fetal Intestine Large	intestine
6	chr4:70043600-70044800	Enhancers	Fetal Intestine Small	intestine
7	chr4:70043600-70045600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr4:70043800-70044800	Weak transcription	Fetal Intestine Large	intestine
9	chr4:70044000-70044600	Enhancers	Cortex derived primary cultured neurospheres	brain
10	chr4:70044200-70044400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr4:70044400-70044600	Enhancers	Liver	Liver
12	chr4:70044400-70045000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr4:70044400-70045400	Enhancers	Stomach Mucosa	stomach
14	chr4:70044600-70045000	Flanking Active TSS	Liver	Liver
15	chr4:70044800-70045000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr4:70044800-70045200	Enhancers	Primary B cells from peripheral blood	blood
17	chr4:70044800-70045400	Flanking Active TSS	Fetal Intestine Small	intestine
18	chr4:70044800-70045600	Enhancers	Fetal Intestine Large	intestine
19	chr4:70045000-70045200	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr4:70045000-70045200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr4:70045000-70045600	Enhancers	Duodenum Mucosa	Duodenum
22	chr4:70045000-70045600	Enhancers	HepG2	liver
23	chr4:70045000-70045800	Enhancers	Primary hematopoietic stem cells	blood
24	chr4:70045000-70046200	Enhancers	Liver	Liver
25	chr4:70045200-70046200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr4:70045200-70047400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr4:70045400-70045600	Enhancers	Fetal Intestine Small	intestine
28	chr4:70045600-70046600	Weak transcription	HepG2	liver
29	chr4:70046200-70047400	Weak transcription	Liver	Liver
30	chr4:70046600-70046800	Enhancers	HepG2	liver
31	chr4:70046800-70047400	Weak transcription	HepG2	liver
32	chr4:70047200-70048000	Enhancers	Primary hematopoietic stem cells short term culture	blood
33	chr4:70047400-70047600	Enhancers	Liver	Liver
34	chr4:70047400-70047600	Enhancers	HepG2	liver
35	chr4:70047400-70048000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr4:70056400-70057600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
37	chr4:70056400-70058400	Enhancers	HepG2	liver
38	chr4:70057400-70058000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr4:70057600-70057800	Enhancers	Liver	Liver
40	chr4:70058200-70058400	ZNF genes & repeats	Liver	Liver
41	chr4:70058400-70059000	Weak transcription	Liver	Liver
42	chr4:70059000-70059800	Enhancers	Liver	Liver
43	chr4:70059800-70060400	Enhancers	HepG2	liver
44	chr4:70059800-70066800	Weak transcription	Liver	Liver
45	chr4:70060000-70060400	Enhancers	Stomach Mucosa	stomach
46	chr4:70060000-70060800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr4:70062000-70063200	Enhancers	HMEC	breast
48	chr4:70062400-70063000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr4:70062600-70063400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
50	chr4:70066800-70067800	Strong transcription	Liver	Liver

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