Variant report

Variant	nsv1003329
Chromosome Location	chr4:70148865-70268857
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	chr4:70210667-70210694	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:70254846-70255212	HepG2	liver:	n/a	n/a
3	ATF1	chr4:70187845-70188142	K562	blood:	n/a	n/a
4	ATF1	chr4:70175307-70175700	K562	blood:	n/a	n/a
5	BHLHE40	chr4:70209675-70209715	K562	blood:	n/a	n/a
6	CBX3	chr4:70175213-70175493	K562	blood:	n/a	n/a
7	CEBPB	chr4:70221057-70221267	HepG2	liver:	n/a	n/a
8	CEBPB	chr4:70209480-70209728	K562	blood:	n/a	n/a
9	CEBPB	chr4:70226229-70226403	HepG2	liver:	n/a	chr4:70226280-70226289 chr4:70226280-70226291
10	CEBPB	chr4:70254941-70255152	HepG2	liver:	n/a	n/a
11	CEBPB	chr4:70211562-70211766	HepG2	liver:	n/a	chr4:70211703-70211714
12	CTCF	chr4:70183720-70183870	HEK293	kidney:	n/a	chr4:70183815-70183833 chr4:70183817-70183838
13	CTCF	chr4:70189067-70189346	H1-hESC	embryonic stem cell:	n/a	n/a
14	CTCF	chr4:70201227-70201509	A549	lung:	n/a	n/a
15	CTCF	chr4:70189165-70189243	K562	blood:	n/a	n/a
16	CTCF	chr4:70243413-70243568	MCF-7	breast:	n/a	n/a
17	CTCF	chr4:70183700-70183850	GM12878	blood:	n/a	chr4:70183815-70183833 chr4:70183817-70183838
18	CTCF	chr4:70183730-70183897	GM13976	blood:	n/a	chr4:70183815-70183833 chr4:70183817-70183838
19	CTCF	chr4:70183675-70183866	ProgFib	skin:	n/a	chr4:70183815-70183833 chr4:70183817-70183838
20	CTCF	chr4:70183642-70183947	GM12878	blood:	n/a	chr4:70183815-70183833 chr4:70183817-70183838
21	CTCF	chr4:70183700-70183850	HBMEC	blood vessel:	n/a	chr4:70183815-70183833 chr4:70183817-70183838
22	CTCF	chr4:70183740-70183890	AG04449	skin:	n/a	chr4:70183815-70183833 chr4:70183817-70183838
23	CTCF	chr4:70201203-70201473	H1-hESC	embryonic stem cell:	n/a	n/a
24	CTCF	chr4:70183688-70183854	NHEK	skin:	n/a	chr4:70183815-70183833 chr4:70183817-70183838
25	CTCF	chr4:70183780-70183930	GM12872	blood:	n/a	chr4:70183815-70183833 chr4:70183817-70183838
26	CTCF	chr4:70201300-70201450	HPF	lung:	n/a	n/a
27	CTCF	chr4:70183600-70183750	HMEC	breast:	n/a	n/a
28	CTCF	chr4:70262525-70262579	GM13977	blood:	n/a	n/a
29	CTCF	chr4:70183655-70183946	MCF-7	breast:	n/a	chr4:70183815-70183833 chr4:70183817-70183838
30	CTCF	chr4:70189240-70189390	HAc	cerebellar:	n/a	n/a
31	CTCF	chr4:70201197-70201460	A549	lung:	n/a	n/a
32	CTCF	chr4:70183672-70183943	H1-hESC	embryonic stem cell:	n/a	chr4:70183815-70183833 chr4:70183817-70183838
33	CTCF	chr4:70183580-70183730	A549	lung:	n/a	n/a
34	CTCF	chr4:70183720-70183870	AG09319	gingival:	n/a	chr4:70183815-70183833 chr4:70183817-70183838
35	CTCF	chr4:70183700-70183850	GM12874	blood:	n/a	chr4:70183815-70183833 chr4:70183817-70183838
36	CTCF	chr4:70183780-70183930	A549	lung:	n/a	chr4:70183815-70183833 chr4:70183817-70183838
37	CTCF	chr4:70183680-70183830	GM12871	blood:	n/a	n/a
38	CTCF	chr4:70183680-70183905	GM20000	blood:	n/a	chr4:70183815-70183833 chr4:70183817-70183838
39	CTCF	chr4:70189200-70189350	NHEK	skin:	n/a	n/a
40	CTCF	chr4:70183687-70183855	GM19238	blood:	n/a	chr4:70183815-70183833 chr4:70183817-70183838
41	CTCF	chr4:70183700-70183850	GM12866	blood:	n/a	chr4:70183815-70183833 chr4:70183817-70183838
42	CTCF	chr4:70183706-70183971	A549	lung:	n/a	chr4:70183815-70183833 chr4:70183817-70183838
43	CTCF	chr4:70183780-70183930	HCM	heart:	n/a	chr4:70183815-70183833 chr4:70183817-70183838
44	CTCF	chr4:70267641-70267711	GM13976	blood:	n/a	n/a
45	CTCF	chr4:70212145-70212187	GM10266	blood:	n/a	n/a
46	CTCF	chr4:70183800-70183950	HRPEpiC	eye:	n/a	chr4:70183815-70183833 chr4:70183817-70183838
47	CTCF	chr4:70209548-70209602	Lung_OC	lung:	n/a	n/a
48	CTCF	chr4:70183740-70183890	GM12875	blood:	n/a	chr4:70183815-70183833 chr4:70183817-70183838
49	CTCF	chr4:70183693-70183935	GM10248	blood:	n/a	chr4:70183815-70183833 chr4:70183817-70183838
50	CTCF	chr4:70261363-70261423	Kidney_OC	kidney:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:70155747-70155797	PrEC	prostate:	n/a
2	chr4:70155747-70155797	PrEC	prostate:	n/a
3	chr4:70155747-70155797	HEK293	kidney:	embryo
4	chr4:70155747-70155797	LNCaP	prostate:	n/a
5	chr4:70155747-70155797	PANC-1	pancreas:	n/a
6	chr4:70155747-70155797	Hela-S3	cervix:	n/a
7	chr4:70155747-70155797	RPTEC	kidney:	n/a
8	chr4:70155747-70155797	AG04449	skin:	fetal
9	chr4:70155747-70155797	NT2-D1	testis:	n/a
10	chr4:70155747-70155797	SKMC	muscle:	n/a
11	chr4:70155747-70155797	AG09319	gingival:	n/a
12	chr4:70155747-70155797	ECC-1	luminal epithelium:	n/a
13	chr4:70155747-70155797	Jurkat	blood:	n/a
14	chr4:70155747-70155797	HCM	heart:	n/a
15	chr4:70155747-70155797	CMK	blood:	n/a
16	chr4:70155747-70155797	HCPEpiC	choroid plexus:	n/a
17	chr4:70155747-70155797	MCF10A-Er-Src	breast:	n/a
18	chr4:70155747-70155797	NHBE	bronchial:	n/a
19	chr4:70155747-70155797	T-47D	breast:	n/a
20	chr4:70155747-70155797	HEEpiC	esophagus:	n/a
21	chr4:70155747-70155797	HMEC	breast:	n/a
22	chr4:70155747-70155797	Caco-2	colon:	n/a
23	chr4:70155747-70155797	HNPCEpiC	eye:	n/a
24	chr4:70155747-70155797	NHDF-neo	bronchial:	n/a
25	chr4:70155747-70155797	AG09309	skin:	n/a
26	chr4:70155747-70155797	HRE	kidney:	n/a
27	chr4:70155747-70155797	A549	lung:	n/a
28	chr4:70155747-70155797	NB4	blood:	n/a
29	chr4:70155747-70155797	GM12891	blood:	n/a
30	chr4:70155747-70155797	SK-N-SH_RA	brain:	n/a
31	chr4:70155747-70155797	NH-A	brain:	n/a
32	chr4:70155747-70155797	BJ	skin:	n/a
33	chr4:70155747-70155797	U87	brain:	n/a
34	chr4:70155747-70155797	ovcar-3	ovarian:	n/a
35	chr4:70155747-70155797	SAEC	small airway:	n/a
36	chr4:70155747-70155797	ProgFib	skin:	n/a
37	chr4:70155747-70155797	SK-N-MC	brain:	n/a
38	chr4:70155747-70155797	GM12878	blood:	n/a
39	chr4:70155747-70155797	GM19239	blood:	n/a
40	chr4:70155747-70155797	PFSK-1	brain:	n/a
41	chr4:70155747-70155797	Hepatocyte	liver:	n/a
42	chr4:70155747-70155797	H1-hESC	embryonic stem cell:	embryo
43	chr4:70155747-70155797	HRPEpiC	eye:	n/a
44	chr4:70155747-70155797	K562	blood:	n/a
45	chr4:70155747-70155797	HPAEpiC	pulmonary alveolar:	n/a
46	chr4:70155747-70155797	IMR90	lung:	fetal
47	chr4:70155747-70155797	AG04450	lung:	fetal
48	chr4:70155747-70155797	HCT-116	colon:	n/a
49	chr4:70155747-70155797	AG10803	skin:	n/a
50	chr4:70155747-70155797	AoSMC	blood vessel:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:70183340..70184245-chr4:70482427..70483057,3	MCF-7	breast:
2	chr4:70183605..70184238-chr4:70482598..70483352,3	MCF-7	breast:
3	chr4:70188461..70190645-chr4:70191525..70193153,2	K562	blood:
4	chr4:70188461..70190645-chr4:70191525..70193153,2	K562	blood:
5	chr4:70262708..70264895-chr4:70280098..70283006,2	K562	blood:
6	chr20:45932378..45933054-chr4:70163468..70164237,2	MCF-7	breast:
7	chr4:69789542..69791043-chr4:70152702..70154403,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-UGT2B28-4	chr4:70253298-70254025	NONHSAT096763

Variant related genes	Relation type
ENSG00000268209	TF binding region
ENSG00000251691	TF binding region
ENSG00000248824	TF binding region
ENSG00000215110	TF binding region
ENSG00000250612	TF binding region
ENSG00000268209	CpG island
ENSG00000251691	CpG island
ENSG00000248824	CpG island
ENSG00000215110	CpG island
ENSG00000250612	CpG island
ENSG00000198277	chromatin interactions

Extended variants
information (count: 1416 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:1416 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs188160642	chr4:70152712-70152713	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs116614850	chr4:70152741-70152742	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs563115462	chr4:70152751-70152752	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs193090565	chr4:70152757-70152758	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs551611980	chr4:70152795-70152796	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs571598594	chr4:70152802-70152803	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs527649511	chr4:70152809-70152810	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs11726210	chr4:70152810-70152811	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs567173327	chr4:70152813-70152814	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs151334448	chr4:70152823-70152824	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs183253998	chr4:70152828-70152829	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs188668542	chr4:70152832-70152833	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs538326744	chr4:70152835-70152836	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs192419407	chr4:70152856-70152857	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs184967506	chr4:70152859-70152860	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs140597679	chr4:70152868-70152869	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs188214818	chr4:70152870-70152871	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs150047201	chr4:70152885-70152886	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs146593078	chr4:70152890-70152891	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs191528217	chr4:70152943-70152944	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs184146381	chr4:70152957-70152958	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs539038894	chr4:70152974-70152975	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs189420405	chr4:70152998-70152999	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs556427025	chr4:70152999-70153000	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs577762086	chr4:70153021-70153022	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs576741874	chr4:70153029-70153030	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs545597651	chr4:70153078-70153079	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs565202969	chr4:70153103-70153104	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs181389317	chr4:70153135-70153136	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs186645465	chr4:70153149-70153150	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs560991031	chr4:70153200-70153201	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs367569821	chr4:70153211-70153212	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs190305356	chr4:70153327-70153328	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs535310230	chr4:70153339-70153340	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs555118888	chr4:70153343-70153344	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs549694135	chr4:70153381-70153382	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs370652124	chr4:70153385-70153386	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs3901337	chr4:70153402-70153403	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs181832942	chr4:70153422-70153423	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs552371020	chr4:70153455-70153456	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs186384300	chr4:70153458-70153459	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs534755747	chr4:70153488-70153489	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs554601888	chr4:70153537-70153538	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs112236446	chr4:70153658-70153659	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs113466652	chr4:70153662-70153663	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs572028947	chr4:70153695-70153696	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs541140739	chr4:70153742-70153743	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs556859324	chr4:70153759-70153760	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs576828617	chr4:70153773-70153774	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs557943236	chr4:70153783-70153784	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:89)

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
Pancreatic cancer	17952125	CNVD
early-passage human iPS cells	21368824	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Schizophrenia	20967226	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD
Oral cancer	21386901	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Chronic lymphocytic leukemia	21215367	CNVD

Chromatin state (count:88 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:70174000-70176000	Enhancers	Stomach Mucosa	stomach
2	chr4:70174200-70175000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr4:70174400-70174600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr4:70174400-70176400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr4:70174600-70175400	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr4:70174600-70175400	Enhancers	HepG2	liver
7	chr4:70174600-70176200	Enhancers	Fetal Intestine Large	intestine
8	chr4:70174600-70176200	Enhancers	Fetal Intestine Small	intestine
9	chr4:70174800-70175200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
10	chr4:70174800-70176600	Enhancers	Primary hematopoietic stem cells short term culture	blood
11	chr4:70175000-70175800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr4:70175000-70176000	Enhancers	Rectal Mucosa Donor 31	rectum
13	chr4:70175800-70176800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr4:70176000-70181400	Weak transcription	Stomach Mucosa	stomach
15	chr4:70176600-70178600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
16	chr4:70176800-70183400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr4:70178600-70178800	Enhancers	Primary hematopoietic stem cells short term culture	blood
18	chr4:70178800-70179000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
19	chr4:70181400-70181800	Enhancers	Stomach Mucosa	stomach
20	chr4:70181800-70183400	Weak transcription	Stomach Mucosa	stomach
21	chr4:70183400-70183600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
22	chr4:70183400-70183800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr4:70183400-70184000	Enhancers	Stomach Mucosa	stomach
24	chr4:70183600-70183800	Enhancers	Primary hematopoietic stem cells short term culture	blood
25	chr4:70183800-70186600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
26	chr4:70183800-70187600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr4:70184000-70186600	Weak transcription	Stomach Mucosa	stomach
28	chr4:70186600-70187200	Enhancers	HSMMtube	muscle
29	chr4:70186600-70188400	Enhancers	Primary hematopoietic stem cells short term culture	blood
30	chr4:70186600-70188400	Enhancers	Fetal Intestine Large	intestine
31	chr4:70186600-70189600	Enhancers	Stomach Mucosa	stomach
32	chr4:70186800-70187400	Enhancers	K562	blood
33	chr4:70186800-70187600	Enhancers	HSMM	muscle
34	chr4:70186800-70187800	Enhancers	Esophagus	oesophagus
35	chr4:70186800-70188000	Enhancers	Gastric	stomach
36	chr4:70186800-70188000	Enhancers	Pancreas	Pancrea
37	chr4:70186800-70188400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
38	chr4:70187000-70187400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr4:70187000-70187600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chr4:70187000-70187800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr4:70187000-70187800	Enhancers	Liver	Liver
42	chr4:70187000-70188000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr4:70187000-70188400	Enhancers	HMEC	breast
44	chr4:70187200-70187800	Flanking Active TSS	HSMMtube	muscle
45	chr4:70187200-70188400	Enhancers	Muscle Satellite Cultured Cells	--
46	chr4:70187400-70188000	Enhancers	Skeletal Muscle Male	skeletal muscle
47	chr4:70187400-70188400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
48	chr4:70187400-70188400	Weak transcription	K562	blood
49	chr4:70187400-70188400	Enhancers	NH-A	brain
50	chr4:70187600-70188000	Enhancers	ES-I3 Cell Line	embryonic stem cell

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