Variant report

Variant	esv1851225
Chromosome Location	chr4:70026366-70230100
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1155)
CpG islands
(count:305)
Chromatin interactive
region (count:11)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1155 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:70036297-70036563	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:70047409-70047599	HepG2	liver:	n/a	n/a
3	ARID3A	chr4:70045525-70045926	HepG2	liver:	n/a	n/a
4	ARID3A	chr4:70080605-70080753	HepG2	liver:	n/a	n/a
5	ARID3A	chr4:70056442-70056604	HepG2	liver:	n/a	n/a
6	ARID3A	chr4:70105540-70105900	HepG2	liver:	n/a	n/a
7	ARID3A	chr4:70105523-70105754	K562	blood:	n/a	n/a
8	ARID3A	chr4:70210667-70210694	HepG2	liver:	n/a	n/a
9	ARID3A	chr4:70106482-70106878	HepG2	liver:	n/a	n/a
10	ATF1	chr4:70033053-70033356	K562	blood:	n/a	n/a
11	ATF1	chr4:70087666-70087866	K562	blood:	n/a	n/a
12	ATF1	chr4:70187845-70188142	K562	blood:	n/a	n/a
13	ATF1	chr4:70044510-70044858	K562	blood:	n/a	n/a
14	ATF1	chr4:70105493-70105808	K562	blood:	n/a	n/a
15	ATF1	chr4:70175307-70175700	K562	blood:	n/a	n/a
16	ATF2	chr4:70032979-70033329	GM12878	blood:	n/a	n/a
17	ATF2	chr4:70033061-70033352	GM12878	blood:	n/a	n/a
18	BACH1	chr4:70036465-70036545	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr4:70033076-70033245	K562	blood:	n/a	n/a
20	BACH1	chr4:70097393-70097475	K562	blood:	n/a	n/a
21	BATF	chr4:70033033-70033336	GM12878	blood:	n/a	chr4:70033221-70033232
22	BCL3	chr4:70080358-70080837	A549	lung:	n/a	n/a
23	BHLHE40	chr4:70057696-70057810	K562	blood:	n/a	n/a
24	BHLHE40	chr4:70087582-70087589	K562	blood:	n/a	n/a
25	BHLHE40	chr4:70044628-70044869	K562	blood:	n/a	n/a
26	BHLHE40	chr4:70047447-70047661	HepG2	liver:	n/a	n/a
27	BHLHE40	chr4:70105574-70105707	K562	blood:	n/a	n/a
28	BHLHE40	chr4:70209675-70209715	K562	blood:	n/a	n/a
29	CBX3	chr4:70033108-70033324	K562	blood:	n/a	n/a
30	CBX3	chr4:70033000-70033366	K562	blood:	n/a	n/a
31	CBX3	chr4:70175213-70175493	K562	blood:	n/a	n/a
32	CCNT2	chr4:70105530-70105702	K562	blood:	n/a	n/a
33	CEBPB	chr4:70045638-70045779	HepG2	liver:	n/a	n/a
34	CEBPB	chr4:70044638-70044861	K562	blood:	n/a	n/a
35	CEBPB	chr4:70221057-70221267	HepG2	liver:	n/a	n/a
36	CEBPB	chr4:70044569-70044904	K562	blood:	n/a	n/a
37	CEBPB	chr4:70077881-70078188	HepG2	liver:	n/a	chr4:70078030-70078041 chr4:70078032-70078043
38	CEBPB	chr4:70105548-70105721	K562	blood:	n/a	n/a
39	CEBPB	chr4:70045536-70045885	HepG2	liver:	n/a	n/a
40	CEBPB	chr4:70077864-70078215	IMR90	lung:	n/a	chr4:70078030-70078041 chr4:70078032-70078043
41	CEBPB	chr4:70047441-70047516	HepG2	liver:	n/a	n/a
42	CEBPB	chr4:70209480-70209728	K562	blood:	n/a	n/a
43	CEBPB	chr4:70226229-70226403	HepG2	liver:	n/a	chr4:70226280-70226289 chr4:70226280-70226291
44	CEBPB	chr4:70080509-70080873	A549	lung:	n/a	n/a
45	CEBPB	chr4:70148592-70148690	A549	lung:	n/a	chr4:70148623-70148634
46	CEBPB	chr4:70046596-70046924	HepG2	liver:	n/a	chr4:70046754-70046765 chr4:70046753-70046764
47	CEBPB	chr4:70105462-70105782	K562	blood:	n/a	n/a
48	CEBPB	chr4:70106514-70106708	HepG2	liver:	n/a	n/a
49	CEBPB	chr4:70077980-70078075	K562	blood:	n/a	chr4:70078030-70078041 chr4:70078032-70078043
50	CEBPB	chr4:70107648-70107863	HepG2	liver:	n/a	chr4:70107721-70107732 chr4:70107722-70107733

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:70080453-70080503	LNCaP	prostate:	n/a
2	chr4:70155747-70155797	IMR90	lung:	fetal
3	chr4:70080453-70080503	PANC-1	pancreas:	n/a
4	chr4:70080453-70080503	HL-60	blood:	n/a
5	chr4:70066318-70066368	GM06990	blood:	n/a
6	chr4:70155747-70155797	SAEC	small airway:	n/a
7	chr4:70064835-70064885	HRE	kidney:	n/a
8	chr4:70064835-70064885	ovcar-3	ovarian:	n/a
9	chr4:70065325-70065375	HCT-116	colon:	n/a
10	chr4:70155747-70155797	Jurkat	blood:	n/a
11	chr4:70080453-70080503	HRPEpiC	eye:	n/a
12	chr4:70065325-70065375	AG09319	gingival:	n/a
13	chr4:70080453-70080503	K562	blood:	n/a
14	chr4:70065325-70065375	HCPEpiC	choroid plexus:	n/a
15	chr4:70066318-70066368	AG10803	skin:	n/a
16	chr4:70065325-70065375	SK-N-SH	brain:	n/a
17	chr4:70066318-70066368	HNPCEpiC	eye:	n/a
18	chr4:70064835-70064885	SK-N-SH	brain:	n/a
19	chr4:70155747-70155797	SK-N-MC	brain:	n/a
20	chr4:70065325-70065375	NT2-D1	testis:	n/a
21	chr4:70065325-70065375	HRCEpiC	kidney:	n/a
22	chr4:70080453-70080503	IMR90	lung:	fetal
23	chr4:70066318-70066368	NT2-D1	testis:	n/a
24	chr4:70155747-70155797	HUVEC	blood vessel:	n/a
25	chr4:70064835-70064885	NHDF-neo	bronchial:	n/a
26	chr4:70064835-70064885	AG09319	gingival:	n/a
27	chr4:70065325-70065375	AG09309	skin:	n/a
28	chr4:70080453-70080503	AG09319	gingival:	n/a
29	chr4:70065325-70065375	RPTEC	kidney:	n/a
30	chr4:70064835-70064885	HCT-116	colon:	n/a
31	chr4:70155747-70155797	NB4	blood:	n/a
32	chr4:70065325-70065375	HL-60	blood:	n/a
33	chr4:70065325-70065375	NHDF-neo	bronchial:	n/a
34	chr4:70064835-70064885	GM12892	blood:	n/a
35	chr4:70065325-70065375	GM06990	blood:	n/a
36	chr4:70064835-70064885	CMK	blood:	n/a
37	chr4:70155747-70155797	MCF10A-Er-Src	breast:	n/a
38	chr4:70065325-70065375	SAEC	small airway:	n/a
39	chr4:70064835-70064885	AG04449	skin:	fetal
40	chr4:70064835-70064885	SK-N-MC	brain:	n/a
41	chr4:70080453-70080503	Jurkat	blood:	n/a
42	chr4:70080453-70080503	GM12892	blood:	n/a
43	chr4:70080453-70080503	A549	lung:	n/a
44	chr4:70155747-70155797	HPAEpiC	pulmonary alveolar:	n/a
45	chr4:70064835-70064885	HPAEpiC	pulmonary alveolar:	n/a
46	chr4:70155747-70155797	NHBE	bronchial:	n/a
47	chr4:70066318-70066368	H1-hESC	embryonic stem cell:	embryo
48	chr4:70155747-70155797	AG09319	gingival:	n/a
49	chr4:70065325-70065375	HRE	kidney:	n/a
50	chr4:70064835-70064885	NH-A	brain:	n/a

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:70188461..70190645-chr4:70191525..70193153,2	K562	blood:
2	chr4:69673177..69674687-chr4:70085938..70087696,2	MCF-7	breast:
3	chr4:70060045..70062674-chr4:70067007..70069842,2	MCF-7	breast:
4	chr4:70060045..70062674-chr4:70067007..70069842,2	MCF-7	breast:
5	chr4:70188461..70190645-chr4:70191525..70193153,2	K562	blood:
6	chr4:70024955..70027798-chr4:70029828..70032326,2	K562	blood:
7	chr20:45932378..45933054-chr4:70163468..70164237,2	MCF-7	breast:
8	chr4:70183340..70184245-chr4:70482427..70483057,3	MCF-7	breast:
9	chr4:69789542..69791043-chr4:70152702..70154403,2	MCF-7	breast:
10	chr4:70183605..70184238-chr4:70482598..70483352,3	MCF-7	breast:
11	chr4:70024955..70027798-chr4:70029828..70032326,2	K562	blood:

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

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

No data

Variant related genes	Relation type
ENSG00000251691	TF binding region
ENSG00000196472	TF binding region
ENSG00000250696	TF binding region
ENSG00000268803	TF binding region
UGT2B11	TF binding region
ENSG00000249763	TF binding region
ENSG00000250612	TF binding region
UGT2B28	TF binding region
ENSG00000251691	CpG island
ENSG00000196472	CpG island
ENSG00000250696	CpG island
ENSG00000268803	CpG island
UGT2B11	CpG island
ENSG00000249763	CpG island
ENSG00000250612	CpG island
UGT2B28	CpG island
ENSG00000198277	chromatin interactions

Extended variants
information (count: 4369 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:4369 , 50 per page) page: 1 2 3 4 5 6 7 ... 88

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs145891704	chr4:70026389-70026390	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs540051352	chr4:70026391-70026392	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs550065673	chr4:70026405-70026406	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs138450326	chr4:70026422-70026423	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs141324582	chr4:70026444-70026445	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs150325905	chr4:70026446-70026447	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs562466623	chr4:70026534-70026535	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs531212447	chr4:70026535-70026536	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs189571321	chr4:70026547-70026548	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs181519208	chr4:70026550-70026551	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs186695467	chr4:70026563-70026564	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs547193538	chr4:70026581-70026582	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs567000385	chr4:70026590-70026591	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs535933642	chr4:70026592-70026593	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs190099092	chr4:70026594-70026595	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs575546173	chr4:70026596-70026597	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs548615006	chr4:70026602-70026603	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs75069985	chr4:70026615-70026616	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs557593941	chr4:70026618-70026619	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs568406660	chr4:70026629-70026630	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs540186010	chr4:70026637-70026638	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs553544318	chr4:70026652-70026653	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs181664600	chr4:70026694-70026695	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs542662297	chr4:70026726-70026727	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs186285879	chr4:70026755-70026756	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs112213328	chr4:70026798-70026799	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs191062493	chr4:70026811-70026812	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs182260670	chr4:70026821-70026822	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs554538862	chr4:70026918-70026919	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs186273453	chr4:70026927-70026928	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs547356214	chr4:70026941-70026942	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs567013108	chr4:70026962-70026963	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs137964740	chr4:70026981-70026982	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs577589572	chr4:70026987-70026988	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs191087599	chr4:70027007-70027008	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs149462634	chr4:70027009-70027010	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs541613608	chr4:70027020-70027021	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs557729012	chr4:70027033-70027034	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs183401146	chr4:70027049-70027050	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs188069804	chr4:70027072-70027073	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs78403222	chr4:70027098-70027099	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs548968413	chr4:70027148-70027149	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs190319671	chr4:70027227-70027228	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs556812324	chr4:70027257-70027258	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs182915154	chr4:70027293-70027294	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs187729336	chr4:70027297-70027298	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs77320960	chr4:70027298-70027299	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs143886053	chr4:70027331-70027332	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs183567301	chr4:70027335-70027336	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs138638753	chr4:70027349-70027350	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:91)

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
early-passage human iPS cells	21368824	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Schizophrenia	20967226	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Oral cancer	21386901	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:191 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:70019400-70031200	Weak transcription	HepG2	liver
2	chr4:70030600-70031400	Enhancers	Rectal Smooth Muscle	rectum
3	chr4:70031200-70031400	Enhancers	Rectal Mucosa Donor 29	rectum
4	chr4:70031200-70032600	Enhancers	HepG2	liver
5	chr4:70031400-70032600	Enhancers	Fetal Intestine Large	intestine
6	chr4:70031600-70031800	Enhancers	Liver	Liver
7	chr4:70031800-70035400	Active TSS	Liver	Liver
8	chr4:70032200-70032600	Active TSS	Rectal Mucosa Donor 29	rectum
9	chr4:70032600-70035400	Weak transcription	HepG2	liver
10	chr4:70035000-70035200	ZNF genes & repeats	Fetal Intestine Small	intestine
11	chr4:70035200-70043600	Weak transcription	Fetal Intestine Small	intestine
12	chr4:70035400-70035800	Flanking Active TSS	Liver	Liver
13	chr4:70035400-70036400	Enhancers	HepG2	liver
14	chr4:70035800-70038200	Enhancers	Liver	Liver
15	chr4:70038200-70038600	Weak transcription	Liver	Liver
16	chr4:70038600-70038800	Enhancers	Liver	Liver
17	chr4:70038800-70041000	Weak transcription	Liver	Liver
18	chr4:70041000-70042000	Strong transcription	Liver	Liver
19	chr4:70042000-70044400	Weak transcription	Liver	Liver
20	chr4:70043600-70043800	Enhancers	Fetal Intestine Large	intestine
21	chr4:70043600-70044800	Enhancers	Fetal Intestine Small	intestine
22	chr4:70043600-70045600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
23	chr4:70043800-70044800	Weak transcription	Fetal Intestine Large	intestine
24	chr4:70044000-70044600	Enhancers	Cortex derived primary cultured neurospheres	brain
25	chr4:70044200-70044400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr4:70044400-70044600	Enhancers	Liver	Liver
27	chr4:70044400-70045000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr4:70044400-70045400	Enhancers	Stomach Mucosa	stomach
29	chr4:70044600-70045000	Flanking Active TSS	Liver	Liver
30	chr4:70044800-70045000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr4:70044800-70045200	Enhancers	Primary B cells from peripheral blood	blood
32	chr4:70044800-70045400	Flanking Active TSS	Fetal Intestine Small	intestine
33	chr4:70044800-70045600	Enhancers	Fetal Intestine Large	intestine
34	chr4:70045000-70045200	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr4:70045000-70045200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr4:70045000-70045600	Enhancers	Duodenum Mucosa	Duodenum
37	chr4:70045000-70045600	Enhancers	HepG2	liver
38	chr4:70045000-70045800	Enhancers	Primary hematopoietic stem cells	blood
39	chr4:70045000-70046200	Enhancers	Liver	Liver
40	chr4:70045200-70046200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr4:70045200-70047400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr4:70045400-70045600	Enhancers	Fetal Intestine Small	intestine
43	chr4:70045600-70046600	Weak transcription	HepG2	liver
44	chr4:70046200-70047400	Weak transcription	Liver	Liver
45	chr4:70046600-70046800	Enhancers	HepG2	liver
46	chr4:70046800-70047400	Weak transcription	HepG2	liver
47	chr4:70047200-70048000	Enhancers	Primary hematopoietic stem cells short term culture	blood
48	chr4:70047400-70047600	Enhancers	Liver	Liver
49	chr4:70047400-70047600	Enhancers	HepG2	liver
50	chr4:70047400-70048000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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