Variant report

Variant	nsv879388
Chromosome Location	chr4:70031620-70116088
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:568)
CpG islands
(count:244)
Chromatin interactive
region (count:4)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:568 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:70105523-70105754	K562	blood:	n/a	n/a
2	ARID3A	chr4:70045525-70045926	HepG2	liver:	n/a	n/a
3	ARID3A	chr4:70036297-70036563	HepG2	liver:	n/a	n/a
4	ARID3A	chr4:70106482-70106878	HepG2	liver:	n/a	n/a
5	ARID3A	chr4:70080605-70080753	HepG2	liver:	n/a	n/a
6	ARID3A	chr4:70047409-70047599	HepG2	liver:	n/a	n/a
7	ARID3A	chr4:70056442-70056604	HepG2	liver:	n/a	n/a
8	ARID3A	chr4:70105540-70105900	HepG2	liver:	n/a	n/a
9	ATF1	chr4:70105493-70105808	K562	blood:	n/a	n/a
10	ATF1	chr4:70087666-70087866	K562	blood:	n/a	n/a
11	ATF1	chr4:70033053-70033356	K562	blood:	n/a	n/a
12	ATF1	chr4:70044510-70044858	K562	blood:	n/a	n/a
13	ATF2	chr4:70033061-70033352	GM12878	blood:	n/a	n/a
14	ATF2	chr4:70032979-70033329	GM12878	blood:	n/a	n/a
15	BACH1	chr4:70033076-70033245	K562	blood:	n/a	n/a
16	BACH1	chr4:70097393-70097475	K562	blood:	n/a	n/a
17	BACH1	chr4:70036465-70036545	H1-hESC	embryonic stem cell:	n/a	n/a
18	BATF	chr4:70033033-70033336	GM12878	blood:	n/a	chr4:70033221-70033232
19	BCL3	chr4:70080358-70080837	A549	lung:	n/a	n/a
20	BHLHE40	chr4:70087582-70087589	K562	blood:	n/a	n/a
21	BHLHE40	chr4:70105574-70105707	K562	blood:	n/a	n/a
22	BHLHE40	chr4:70047447-70047661	HepG2	liver:	n/a	n/a
23	BHLHE40	chr4:70057696-70057810	K562	blood:	n/a	n/a
24	BHLHE40	chr4:70044628-70044869	K562	blood:	n/a	n/a
25	CBX3	chr4:70033108-70033324	K562	blood:	n/a	n/a
26	CBX3	chr4:70033000-70033366	K562	blood:	n/a	n/a
27	CCNT2	chr4:70105530-70105702	K562	blood:	n/a	n/a
28	CEBPB	chr4:70045536-70045885	HepG2	liver:	n/a	n/a
29	CEBPB	chr4:70077864-70078215	IMR90	lung:	n/a	chr4:70078030-70078041 chr4:70078032-70078043
30	CEBPB	chr4:70044569-70044904	K562	blood:	n/a	n/a
31	CEBPB	chr4:70077881-70078188	HepG2	liver:	n/a	chr4:70078030-70078041 chr4:70078032-70078043
32	CEBPB	chr4:70107648-70107863	HepG2	liver:	n/a	chr4:70107721-70107732 chr4:70107722-70107733
33	CEBPB	chr4:70046596-70046924	HepG2	liver:	n/a	chr4:70046754-70046765 chr4:70046753-70046764
34	CEBPB	chr4:70106514-70106708	HepG2	liver:	n/a	n/a
35	CEBPB	chr4:70045638-70045779	HepG2	liver:	n/a	n/a
36	CEBPB	chr4:70047441-70047516	HepG2	liver:	n/a	n/a
37	CEBPB	chr4:70044638-70044861	K562	blood:	n/a	n/a
38	CEBPB	chr4:70107631-70107834	A549	lung:	n/a	chr4:70107721-70107732 chr4:70107722-70107733
39	CEBPB	chr4:70105548-70105721	K562	blood:	n/a	n/a
40	CEBPB	chr4:70080509-70080873	A549	lung:	n/a	n/a
41	CEBPB	chr4:70059993-70060205	HepG2	liver:	n/a	n/a
42	CEBPB	chr4:70105462-70105782	K562	blood:	n/a	n/a
43	CEBPB	chr4:70077980-70078075	K562	blood:	n/a	chr4:70078030-70078041 chr4:70078032-70078043
44	CEBPD	chr4:70044512-70044940	K562	blood:	n/a	n/a
45	CEBPD	chr4:70045604-70045791	HepG2	liver:	n/a	n/a
46	CEBPD	chr4:70105414-70105831	K562	blood:	n/a	n/a
47	CREB1	chr4:70033107-70033379	GM12878	blood:	n/a	n/a
48	CREB1	chr4:70045635-70045816	HepG2	liver:	n/a	n/a
49	CREB1	chr4:70033137-70033332	GM12878	blood:	n/a	n/a
50	CTCF	chr4:70036318-70036532	ProgFib	skin:	n/a	chr4:70036404-70036422 chr4:70036399-70036420

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:70080453-70080503	GM06990	blood:	n/a
2	chr4:70065325-70065375	T-47D	breast:	n/a
3	chr4:70080453-70080503	K562	blood:	n/a
4	chr4:70064835-70064885	HRPEpiC	eye:	n/a
5	chr4:70066318-70066368	NHDF-neo	bronchial:	n/a
6	chr4:70066318-70066368	NT2-D1	testis:	n/a
7	chr4:70080453-70080503	HEK293	kidney:	embryo
8	chr4:70066318-70066368	HepG2	liver:	n/a
9	chr4:70080453-70080503	CMK	blood:	n/a
10	chr4:70064835-70064885	AG04449	skin:	fetal
11	chr4:70080453-70080503	SK-N-MC	brain:	n/a
12	chr4:70066318-70066368	U87	brain:	n/a
13	chr4:70064835-70064885	H1-hESC	embryonic stem cell:	embryo
14	chr4:70066318-70066368	HEK293	kidney:	embryo
15	chr4:70065325-70065375	SK-N-SH	brain:	n/a
16	chr4:70080453-70080503	HPAEpiC	pulmonary alveolar:	n/a
17	chr4:70065325-70065375	HCPEpiC	choroid plexus:	n/a
18	chr4:70066318-70066368	GM06990	blood:	n/a
19	chr4:70064835-70064885	BE2_C	brain:	n/a
20	chr4:70080453-70080503	HUVEC	blood vessel:	n/a
21	chr4:70065325-70065375	HepG2	liver:	n/a
22	chr4:70066318-70066368	ECC-1	luminal epithelium:	n/a
23	chr4:70066318-70066368	GM19239	blood:	n/a
24	chr4:70080453-70080503	A549	lung:	n/a
25	chr4:70065325-70065375	HL-60	blood:	n/a
26	chr4:70065325-70065375	U87	brain:	n/a
27	chr4:70080453-70080503	HCT-116	colon:	n/a
28	chr4:70065325-70065375	HCT-116	colon:	n/a
29	chr4:70064835-70064885	PrEC	prostate:	n/a
30	chr4:70065325-70065375	HMEC	breast:	n/a
31	chr4:70066318-70066368	ovcar-3	ovarian:	n/a
32	chr4:70066318-70066368	SAEC	small airway:	n/a
33	chr4:70066318-70066368	Jurkat	blood:	n/a
34	chr4:70065325-70065375	LNCaP	prostate:	n/a
35	chr4:70064835-70064885	RPTEC	kidney:	n/a
36	chr4:70064835-70064885	AG04450	lung:	fetal
37	chr4:70065325-70065375	K562	blood:	n/a
38	chr4:70066318-70066368	AG10803	skin:	n/a
39	chr4:70080453-70080503	GM19239	blood:	n/a
40	chr4:70064835-70064885	HRE	kidney:	n/a
41	chr4:70064835-70064885	HIPEpiC	eye:	n/a
42	chr4:70080453-70080503	NT2-D1	testis:	n/a
43	chr4:70064835-70064885	HepG2	liver:	n/a
44	chr4:70064835-70064885	T-47D	breast:	n/a
45	chr4:70066318-70066368	BJ	skin:	n/a
46	chr4:70066318-70066368	SK-N-MC	brain:	n/a
47	chr4:70065325-70065375	Caco-2	colon:	n/a
48	chr4:70065325-70065375	AG10803	skin:	n/a
49	chr4:70064835-70064885	HNPCEpiC	eye:	n/a
50	chr4:70065325-70065375	H1-hESC	embryonic stem cell:	embryo

(count:4 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:69673177..69674687-chr4:70085938..70087696,2	MCF-7	breast:
2	chr4:70024955..70027798-chr4:70029828..70032326,2	K562	blood:
3	chr4:70060045..70062674-chr4:70067007..70069842,2	MCF-7	breast:
4	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	chr4:70076784-70076865	ENSG00000250696.1
3	lnc-UGT2B28-1	chr4:70061386-70061489	ENSG00000250696.1
4	lnc-UGT2B28-1	chr4:70066890-70067002	ENSG00000250696.1
5	lnc-UGT2B28-1	chr4:70076784-70076865	ENSG00000250696.1
6	lnc-UGT2B28-1	chr4:70080191-70082484	ENSG00000250696.1
7	lnc-UGT2B28-1	chr4:70047378-70048090	NONHSAT096756
8	lnc-UGT2B28-1	chr4:70080191-70080193	ENSG00000250696.1
9	lnc-UGT2B28-1	chr4:70047818-70048090	ENSG00000250696.1
10	lnc-UGT2B28-1	chr4:70066138-70066296	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
ENSG00000249763	TF binding region
ENSG00000196472	CpG island
ENSG00000250696	CpG island
ENSG00000268803	CpG island
UGT2B11	CpG island
ENSG00000249763	CpG island

Extended variants
information (count: 2723 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:2723 , 50 per page) page: 1 2 3 4 5 6 7 ... 55

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4593203	chr4:70031620-70031621	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs561614566	chr4:70031626-70031627	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs528913926	chr4:70031630-70031631	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs4438816	chr4:70031658-70031659	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs184608723	chr4:70031703-70031704	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs6836096	chr4:70031780-70031781	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs57286992	chr4:70031834-70031835	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs550129717	chr4:70031867-70031868	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs569924862	chr4:70031871-70031872	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs4594789	chr4:70031875-70031876	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs573788757	chr4:70031923-70031924	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs61137241	chr4:70031948-70031949	Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs189346057	chr4:70031968-70031969	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs566379383	chr4:70031970-70031971	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs576074686	chr4:70032011-70032012	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs6856940	chr4:70032018-70032019	Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs565977513	chr4:70032031-70032032	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs578184873	chr4:70032047-70032048	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs371737546	chr4:70032070-70032071	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs191113346	chr4:70032076-70032077	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs560438092	chr4:70032095-70032096	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs138180865	chr4:70032112-70032113	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs111801292	chr4:70032147-70032148	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs35526802	chr4:70032170-70032171	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs562656071	chr4:70032198-70032199	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs531720679	chr4:70032211-70032212	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs183753413	chr4:70032261-70032262	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs72855468	chr4:70032280-70032281	Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs114866018	chr4:70032333-70032334	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs144074976	chr4:70032361-70032362	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs115759237	chr4:70032386-70032387	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs148662151	chr4:70032391-70032392	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs72855469	chr4:70032433-70032434	Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs76144847	chr4:70032457-70032458	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs189825232	chr4:70032479-70032480	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs558259031	chr4:70032482-70032483	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs572013951	chr4:70032494-70032495	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs181363331	chr4:70032499-70032500	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs369915648	chr4:70032519-70032520	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs4694668	chr4:70032525-70032526	Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs573859234	chr4:70032541-70032542	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs542792811	chr4:70032542-70032543	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs185217345	chr4:70032547-70032548	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs377110374	chr4:70032552-70032553	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs531684549	chr4:70032591-70032592	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs72855471	chr4:70032596-70032597	Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs565089696	chr4:70032599-70032600	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs527708853	chr4:70032609-70032610	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs189847337	chr4:70032672-70032673	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs567538408	chr4:70032694-70032695	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:85)

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
Non-syndromic sensorineural hearing loss	18451855	CNVD
Glioblastoma multiforme	21510904	CNVD

Chromatin state (count:98 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:70031200-70032600	Enhancers	HepG2	liver
2	chr4:70031400-70032600	Enhancers	Fetal Intestine Large	intestine
3	chr4:70031600-70031800	Enhancers	Liver	Liver
4	chr4:70031800-70035400	Active TSS	Liver	Liver
5	chr4:70032200-70032600	Active TSS	Rectal Mucosa Donor 29	rectum
6	chr4:70032600-70035400	Weak transcription	HepG2	liver
7	chr4:70035000-70035200	ZNF genes & repeats	Fetal Intestine Small	intestine
8	chr4:70035200-70043600	Weak transcription	Fetal Intestine Small	intestine
9	chr4:70035400-70035800	Flanking Active TSS	Liver	Liver
10	chr4:70035400-70036400	Enhancers	HepG2	liver
11	chr4:70035800-70038200	Enhancers	Liver	Liver
12	chr4:70038200-70038600	Weak transcription	Liver	Liver
13	chr4:70038600-70038800	Enhancers	Liver	Liver
14	chr4:70038800-70041000	Weak transcription	Liver	Liver
15	chr4:70041000-70042000	Strong transcription	Liver	Liver
16	chr4:70042000-70044400	Weak transcription	Liver	Liver
17	chr4:70043600-70043800	Enhancers	Fetal Intestine Large	intestine
18	chr4:70043600-70044800	Enhancers	Fetal Intestine Small	intestine
19	chr4:70043600-70045600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
20	chr4:70043800-70044800	Weak transcription	Fetal Intestine Large	intestine
21	chr4:70044000-70044600	Enhancers	Cortex derived primary cultured neurospheres	brain
22	chr4:70044200-70044400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr4:70044400-70044600	Enhancers	Liver	Liver
24	chr4:70044400-70045000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr4:70044400-70045400	Enhancers	Stomach Mucosa	stomach
26	chr4:70044600-70045000	Flanking Active TSS	Liver	Liver
27	chr4:70044800-70045000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr4:70044800-70045200	Enhancers	Primary B cells from peripheral blood	blood
29	chr4:70044800-70045400	Flanking Active TSS	Fetal Intestine Small	intestine
30	chr4:70044800-70045600	Enhancers	Fetal Intestine Large	intestine
31	chr4:70045000-70045200	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr4:70045000-70045200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr4:70045000-70045600	Enhancers	Duodenum Mucosa	Duodenum
34	chr4:70045000-70045600	Enhancers	HepG2	liver
35	chr4:70045000-70045800	Enhancers	Primary hematopoietic stem cells	blood
36	chr4:70045000-70046200	Enhancers	Liver	Liver
37	chr4:70045200-70046200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr4:70045200-70047400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr4:70045400-70045600	Enhancers	Fetal Intestine Small	intestine
40	chr4:70045600-70046600	Weak transcription	HepG2	liver
41	chr4:70046200-70047400	Weak transcription	Liver	Liver
42	chr4:70046600-70046800	Enhancers	HepG2	liver
43	chr4:70046800-70047400	Weak transcription	HepG2	liver
44	chr4:70047200-70048000	Enhancers	Primary hematopoietic stem cells short term culture	blood
45	chr4:70047400-70047600	Enhancers	Liver	Liver
46	chr4:70047400-70047600	Enhancers	HepG2	liver
47	chr4:70047400-70048000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr4:70056400-70057600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
49	chr4:70056400-70058400	Enhancers	HepG2	liver
50	chr4:70057400-70058000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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