Variant report

Variant	nsv470045
Chromosome Location	chr4:70297892-70383991
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:425)
CpG islands
(count:122)
Chromatin interactive
region (count:8)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:425 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:70324166-70324568	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:70383793-70384506	HepG2	liver:	n/a	n/a
3	ARID3A	chr4:70361428-70361936	HepG2	liver:	n/a	n/a
4	ARID3A	chr4:70350802-70351141	HepG2	liver:	n/a	n/a
5	ARID3A	chr4:70359216-70359556	HepG2	liver:	n/a	n/a
6	ATF2	chr4:70333524-70333998	H1-hESC	embryonic stem cell:	n/a	n/a
7	BATF	chr4:70367562-70367758	GM12878	blood:	n/a	chr4:70367695-70367706
8	BHLHE40	chr4:70361410-70361902	HepG2	liver:	n/a	n/a
9	CEBPB	chr4:70359060-70359353	A549	lung:	n/a	chr4:70359161-70359174 chr4:70359163-70359174 chr4:70359161-70359174 chr4:70359161-70359172 chr4:70359235-70359246
10	CEBPB	chr4:70347375-70347559	A549	lung:	n/a	n/a
11	CEBPB	chr4:70302923-70302937	HepG2	liver:	n/a	n/a
12	CEBPB	chr4:70361341-70361664	HepG2	liver:	n/a	n/a
13	CEBPB	chr4:70324137-70324588	HepG2	liver:	n/a	n/a
14	CEBPB	chr4:70383870-70384874	HepG2	liver:	n/a	chr4:70384445-70384456 chr4:70384443-70384454 chr4:70384757-70384769
15	CEBPB	chr4:70339506-70339743	HepG2	liver:	n/a	n/a
16	CEBPB	chr4:70324164-70324515	HepG2	liver:	n/a	n/a
17	CEBPB	chr4:70371476-70371676	HepG2	liver:	n/a	chr4:70371515-70371526
18	CEBPB	chr4:70361482-70361691	HepG2	liver:	n/a	n/a
19	CEBPB	chr4:70361393-70361913	HepG2	liver:	n/a	n/a
20	CEBPB	chr4:70350737-70351236	HepG2	liver:	n/a	chr4:70351083-70351094
21	CEBPB	chr4:70359008-70359609	HepG2	liver:	n/a	chr4:70359161-70359174 chr4:70359163-70359174 chr4:70359161-70359174 chr4:70359161-70359172 chr4:70359235-70359246
22	CEBPB	chr4:70324294-70324494	H1-hESC	embryonic stem cell:	n/a	n/a
23	CEBPB	chr4:70359098-70359325	K562	blood:	n/a	chr4:70359161-70359174 chr4:70359163-70359174 chr4:70359161-70359174 chr4:70359161-70359172 chr4:70359235-70359246
24	CEBPB	chr4:70324212-70324508	HepG2	liver:	n/a	n/a
25	CEBPB	chr4:70333789-70333989	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr4:70319378-70319596	HepG2	liver:	n/a	chr4:70319545-70319556
27	CEBPB	chr4:70324169-70324482	HepG2	liver:	n/a	n/a
28	CEBPB	chr4:70361394-70361769	HepG2	liver:	n/a	n/a
29	CHD1	chr4:70338556-70338566	GM12878	blood:	n/a	n/a
30	CHD2	chr4:70369436-70369565	H1-hESC	embryonic stem cell:	n/a	n/a
31	CHD2	chr4:70369393-70369418	HepG2	liver:	n/a	n/a
32	CTCF	chr4:70336400-70336542	Hela-S3	cervix:	n/a	n/a
33	CTCF	chr4:70383530-70383657	MCF-7	breast:	n/a	n/a
34	CTCF	chr4:70369340-70369490	GM12869	blood:	n/a	n/a
35	CTCF	chr4:70336300-70336450	BE2_C	brain:	n/a	chr4:70336307-70336315
36	CTCF	chr4:70369432-70369511	MCF-7	breast:	n/a	n/a
37	CTCF	chr4:70369354-70369590	H1-hESC	embryonic stem cell:	n/a	n/a
38	CTCF	chr4:70336380-70336530	AoAF	blood vessel:	n/a	n/a
39	CTCF	chr4:70369382-70369565	HepG2	liver:	n/a	n/a
40	CTCF	chr4:70336425-70336501	MCF-7	breast:	n/a	n/a
41	CTCF	chr4:70369432-70369524	MCF-7	breast:	n/a	n/a
42	CTCF	chr4:70369380-70369530	HepG2	liver:	n/a	n/a
43	CTCF	chr4:70369420-70369570	HBMEC	blood vessel:	n/a	n/a
44	CTCF	chr4:70336385-70336569	HepG2	liver:	n/a	n/a
45	CTCF	chr4:70336350-70336602	H1-hESC	embryonic stem cell:	n/a	n/a
46	CTCF	chr4:70336560-70336710	GM12868	blood:	n/a	n/a
47	CTCF	chr4:70369433-70369555	MCF-7	breast:	n/a	n/a
48	CTCF	chr4:70336400-70336550	WERI-Rb-1	eye:	n/a	n/a
49	CTCF	chr4:70369440-70369590	HRPEpiC	eye:	n/a	n/a
50	CTCF	chr4:70369440-70369590	HCT-116	colon:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:70346347-70346397	GM12878	blood:	n/a
2	chr4:70346347-70346397	Caco-2	colon:	n/a
3	chr4:70346347-70346397	HepG2	liver:	n/a
4	chr4:70361062-70361112	HEEpiC	esophagus:	n/a
5	chr4:70346347-70346397	NT2-D1	testis:	n/a
6	chr4:70346347-70346397	NH-A	brain:	n/a
7	chr4:70346347-70346397	SKMC	muscle:	n/a
8	chr4:70361062-70361112	ovcar-3	ovarian:	n/a
9	chr4:70346347-70346397	IMR90	lung:	fetal
10	chr4:70346347-70346397	NB4	blood:	n/a
11	chr4:70361062-70361112	SKMC	muscle:	n/a
12	chr4:70346347-70346397	AG04449	skin:	fetal
13	chr4:70346347-70346397	HPAEpiC	pulmonary alveolar:	n/a
14	chr4:70346347-70346397	ECC-1	luminal epithelium:	n/a
15	chr4:70361062-70361112	HPAEpiC	pulmonary alveolar:	n/a
16	chr4:70346347-70346397	AG09319	gingival:	n/a
17	chr4:70346347-70346397	H1-hESC	embryonic stem cell:	embryo
18	chr4:70346347-70346397	SK-N-SH_RA	brain:	n/a
19	chr4:70361062-70361112	HepG2	liver:	n/a
20	chr4:70361062-70361112	BE2_C	brain:	n/a
21	chr4:70346347-70346397	HCT-116	colon:	n/a
22	chr4:70361062-70361112	SK-N-SH	brain:	n/a
23	chr4:70361062-70361112	IMR90	lung:	fetal
24	chr4:70361062-70361112	Jurkat	blood:	n/a
25	chr4:70361062-70361112	BJ	skin:	n/a
26	chr4:70361062-70361112	GM19239	blood:	n/a
27	chr4:70346347-70346397	Jurkat	blood:	n/a
28	chr4:70361062-70361112	A549	lung:	n/a
29	chr4:70346347-70346397	HCF	heart:	n/a
30	chr4:70361062-70361112	AG04450	lung:	fetal
31	chr4:70361062-70361112	GM12891	blood:	n/a
32	chr4:70346347-70346397	SAEC	small airway:	n/a
33	chr4:70346347-70346397	HCM	heart:	n/a
34	chr4:70346347-70346397	HRE	kidney:	n/a
35	chr4:70361062-70361112	HIPEpiC	eye:	n/a
36	chr4:70346347-70346397	MCF-7	breast:	n/a
37	chr4:70361062-70361112	HEK293	kidney:	embryo
38	chr4:70346347-70346397	A549	lung:	n/a
39	chr4:70361062-70361112	NT2-D1	testis:	n/a
40	chr4:70361062-70361112	AG09309	skin:	n/a
41	chr4:70361062-70361112	GM12892	blood:	n/a
42	chr4:70361062-70361112	RPTEC	kidney:	n/a
43	chr4:70361062-70361112	NHDF-neo	bronchial:	n/a
44	chr4:70361062-70361112	K562	blood:	n/a
45	chr4:70361062-70361112	AG10803	skin:	n/a
46	chr4:70346347-70346397	SK-N-SH	brain:	n/a
47	chr4:70361062-70361112	HNPCEpiC	eye:	n/a
48	chr4:70346347-70346397	BJ	skin:	n/a
49	chr4:70346347-70346397	GM06990	blood:	n/a
50	chr4:70346347-70346397	HMEC	breast:	n/a

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:6797888..6800431-chr4:70351986..70354075,2	MCF-7	breast:
2	chr4:70379330..70381215-chr4:70382030..70384687,2	K562	blood:
3	chr2:169797130..169797902-chr4:70311918..70312713,2	MCF-7	breast:
4	chr2:133011384..133014243-chr4:70295163..70298145,2	K562	blood:
5	chr20:52578439..52580096-chr4:70380828..70382348,2	MCF-7	breast:
6	chr4:70383119..70384022-chr4:70482515..70483454,3	MCF-7	breast:
7	chr21:9824058..9826515-chr4:70295211..70298169,2	K562	blood:
8	chr21:9825015..9827465-chr4:70296669..70298179,2	K562	blood:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-UGT2B28-7	chr4:70317229-70317331	NONHSAT096766
2	lnc-UGT2B28-6	chr4:70303075-70303156	NONHSAT096765
3	lnc-UGT2B28-7	chr4:70315732-70315864	NONHSAT096766
4	lnc-UGT2B28-6	chr4:70304044-70304260	NONHSAT096765
5	lnc-UGT2B28-6	chr4:70306600-70306768	NONHSAT096765

No data

Variant related genes	Relation type
ENSG00000249686	TF binding region
ENSG00000264696	TF binding region
ENSG00000250828	TF binding region
UGT2B4	TF binding region
ENSG00000249686	CpG island
ENSG00000264696	CpG island
ENSG00000250828	CpG island
UGT2B4	CpG island
ENSG00000264462	chromatin interactions
ENSG00000264063	chromatin interactions
ENSG00000126746	chromatin interactions
ENSG00000248886	chromatin interactions

Extended variants
information (count: 2141 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:2141 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs13137023	chr4:70297892-70297893	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs570201090	chr4:70297926-70297927	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs559981339	chr4:70297941-70297942	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs193004012	chr4:70297942-70297943	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs376086965	chr4:70297963-70297964	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs541991885	chr4:70297988-70297989	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs113547466	chr4:70297990-70297991	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs142133137	chr4:70297998-70297999	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs563895395	chr4:70298000-70298001	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs374806061	chr4:70298034-70298035	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs368868103	chr4:70298043-70298044	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs372966842	chr4:70298047-70298048	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs146566910	chr4:70298080-70298081	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs112840795	chr4:70298154-70298155	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs533340319	chr4:70298155-70298156	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs546610074	chr4:70298194-70298195	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs115573176	chr4:70298196-70298197	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs185130514	chr4:70298201-70298202	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs549150197	chr4:70298203-70298204	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs190081769	chr4:70298214-70298215	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs112187006	chr4:70298215-70298216	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs557829664	chr4:70298251-70298252	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs577593886	chr4:70298253-70298254	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs533748241	chr4:70298277-70298278	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs181610525	chr4:70298304-70298305	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs112288143	chr4:70298322-70298323	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs186350451	chr4:70298360-70298361	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs561987962	chr4:70298379-70298380	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs2101793	chr4:70298418-70298419	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
30	rs189532195	chr4:70298514-70298515	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs544330148	chr4:70298533-70298534	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs538034879	chr4:70298548-70298549	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs533184697	chr4:70298553-70298554	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs149646439	chr4:70298575-70298576	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs560189623	chr4:70298582-70298583	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs546926484	chr4:70298606-70298607	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs144373398	chr4:70298666-70298667	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs567073584	chr4:70298669-70298670	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs539285969	chr4:70298677-70298678	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs549289002	chr4:70298680-70298681	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs180812091	chr4:70298681-70298682	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs112616322	chr4:70298696-70298697	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs186205602	chr4:70298703-70298704	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs2088092	chr4:70298721-70298722	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
45	rs571293370	chr4:70298722-70298723	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs111395656	chr4:70298730-70298731	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs142224964	chr4:70298775-70298776	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs142108933	chr4:70298776-70298777	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs371205645	chr4:70298777-70298778	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs397745595	chr4:70298780-70298781	Weak transcription	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
T-cell prolymphocytic leukemia	19278963	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
small cell lung cancer	20016488	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:74 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:70297000-70298800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
2	chr4:70297000-70300400	Weak transcription	Liver	Liver
3	chr4:70298800-70299000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
4	chr4:70300400-70300800	Enhancers	Liver	Liver
5	chr4:70309600-70310200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
6	chr4:70310200-70312400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
7	chr4:70312200-70312600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr4:70312400-70313000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
9	chr4:70321400-70322000	Enhancers	HepG2	liver
10	chr4:70321400-70322200	Enhancers	Liver	Liver
11	chr4:70322000-70323400	Weak transcription	HepG2	liver
12	chr4:70322200-70323400	Weak transcription	Liver	Liver
13	chr4:70323400-70324000	Enhancers	Liver	Liver
14	chr4:70323400-70325200	Enhancers	HepG2	liver
15	chr4:70324000-70324200	Flanking Active TSS	Liver	Liver
16	chr4:70324200-70324400	Enhancers	Liver	Liver
17	chr4:70324200-70324600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr4:70324400-70324600	Flanking Active TSS	Liver	Liver
19	chr4:70324600-70325200	Enhancers	Liver	Liver
20	chr4:70333000-70334200	Enhancers	HUES6 Cell Line	embryonic stem cell
21	chr4:70333200-70333600	Enhancers	iPS-18 Cell Line	embryonic stem cell
22	chr4:70333200-70333800	Enhancers	H1 Cell Line	embryonic stem cell
23	chr4:70333200-70334000	Enhancers	H9 Cell Line	embryonic stem cell
24	chr4:70339400-70339800	Enhancers	HepG2	liver
25	chr4:70339400-70340000	Enhancers	Liver	Liver
26	chr4:70340000-70344200	Weak transcription	Liver	Liver
27	chr4:70344200-70350200	Strong transcription	Liver	Liver
28	chr4:70350200-70352000	Genic enhancers	Liver	Liver
29	chr4:70352000-70354400	Strong transcription	Liver	Liver
30	chr4:70354400-70357000	Genic enhancers	Liver	Liver
31	chr4:70355800-70356200	Enhancers	Fetal Lung	lung
32	chr4:70356000-70356600	Enhancers	HSMM	muscle
33	chr4:70356200-70356600	Enhancers	HSMMtube	muscle
34	chr4:70356600-70362600	Weak transcription	HSMM	muscle
35	chr4:70357000-70359200	Transcr. at gene 5' and 3'	Liver	Liver
36	chr4:70358800-70362200	Enhancers	HepG2	liver
37	chr4:70359200-70362200	Active TSS	Liver	Liver
38	chr4:70360200-70361400	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr4:70361200-70362000	Enhancers	Fetal Intestine Small	intestine
40	chr4:70361400-70362800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr4:70362200-70363000	Enhancers	Liver	Liver
42	chr4:70362400-70363400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
43	chr4:70362600-70363400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
44	chr4:70362600-70364200	Enhancers	HSMM	muscle
45	chr4:70362600-70364200	Enhancers	NH-A	brain
46	chr4:70362800-70363000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr4:70363000-70363400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr4:70363000-70363600	Enhancers	HSMMtube	muscle
49	chr4:70363000-70364000	Weak transcription	Liver	Liver
50	chr4:70363200-70364200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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