Variant report

Variant	nsv594584
Chromosome Location	chr4:70057009-70171280
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:377)
CpG islands
(count:305)
Chromatin interactive
region (count:5)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:377 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:70080605-70080753	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:70106482-70106878	HepG2	liver:	n/a	n/a
3	ARID3A	chr4:70105540-70105900	HepG2	liver:	n/a	n/a
4	ARID3A	chr4:70105523-70105754	K562	blood:	n/a	n/a
5	ATF1	chr4:70087666-70087866	K562	blood:	n/a	n/a
6	ATF1	chr4:70105493-70105808	K562	blood:	n/a	n/a
7	BACH1	chr4:70097393-70097475	K562	blood:	n/a	n/a
8	BCL3	chr4:70080358-70080837	A549	lung:	n/a	n/a
9	BHLHE40	chr4:70087582-70087589	K562	blood:	n/a	n/a
10	BHLHE40	chr4:70057696-70057810	K562	blood:	n/a	n/a
11	BHLHE40	chr4:70105574-70105707	K562	blood:	n/a	n/a
12	CCNT2	chr4:70105530-70105702	K562	blood:	n/a	n/a
13	CEBPB	chr4:70148603-70148719	H1-hESC	embryonic stem cell:	n/a	chr4:70148623-70148634
14	CEBPB	chr4:70080509-70080873	A549	lung:	n/a	n/a
15	CEBPB	chr4:70077980-70078075	K562	blood:	n/a	chr4:70078030-70078041 chr4:70078032-70078043
16	CEBPB	chr4:70077881-70078188	HepG2	liver:	n/a	chr4:70078030-70078041 chr4:70078032-70078043
17	CEBPB	chr4:70105548-70105721	K562	blood:	n/a	n/a
18	CEBPB	chr4:70105462-70105782	K562	blood:	n/a	n/a
19	CEBPB	chr4:70118972-70119263	HepG2	liver:	n/a	chr4:70119163-70119176
20	CEBPB	chr4:70148592-70148690	A549	lung:	n/a	chr4:70148623-70148634
21	CEBPB	chr4:70059993-70060205	HepG2	liver:	n/a	n/a
22	CEBPB	chr4:70107648-70107863	HepG2	liver:	n/a	chr4:70107721-70107732 chr4:70107722-70107733
23	CEBPB	chr4:70077864-70078215	IMR90	lung:	n/a	chr4:70078030-70078041 chr4:70078032-70078043
24	CEBPB	chr4:70106514-70106708	HepG2	liver:	n/a	n/a
25	CEBPB	chr4:70107631-70107834	A549	lung:	n/a	chr4:70107721-70107732 chr4:70107722-70107733
26	CEBPB	chr4:70148545-70148642	K562	blood:	n/a	chr4:70148623-70148634
27	CEBPD	chr4:70105414-70105831	K562	blood:	n/a	n/a
28	CTCF	chr4:70134439-70134557	K562	blood:	n/a	n/a
29	CTCF	chr4:70105505-70105507	LNCaP	prostate:	n/a	n/a
30	CTCF	chr4:70142506-70142627	GM13976	blood:	n/a	n/a
31	CTCF	chr4:70089080-70089230	HepG2	liver:	n/a	n/a
32	CTCF	chr4:70155388-70155482	Kidney_OC	kidney:	n/a	n/a
33	CTCF	chr4:70081934-70082033	GM10248	blood:	n/a	n/a
34	CTCF	chr4:70134463-70134574	A549	lung:	n/a	n/a
35	CTCF	chr4:70077161-70077220	Kidney_OC	kidney:	n/a	n/a
36	CTCF	chr4:70147051-70147132	GM20000	blood:	n/a	n/a
37	CTCF	chr4:70089077-70089312	MCF-7	breast:	n/a	n/a
38	CTCF	chr4:70116400-70116414	Lung_OC	lung:	n/a	n/a
39	CTCF	chr4:70116866-70116969	Kidney_OC	kidney:	n/a	n/a
40	CTCF	chr4:70134427-70134585	MCF-7	breast:	n/a	n/a
41	CTCF	chr4:70105486-70105552	K562	blood:	n/a	n/a
42	CTCF	chr4:70134412-70134589	HepG2	liver:	n/a	n/a
43	CTCF	chr4:70134440-70134590	WERI-Rb-1	eye:	n/a	n/a
44	CTCF	chr4:70089120-70089270	WERI-Rb-1	eye:	n/a	n/a
45	CTCF	chr4:70097033-70097046	GM13977	blood:	n/a	n/a
46	CTCF	chr4:70134452-70134606	H1-hESC	embryonic stem cell:	n/a	n/a
47	CTCF	chr4:70089126-70089248	MCF-7	breast:	n/a	n/a
48	CTCF	chr4:70105384-70105645	K562	blood:	n/a	n/a
49	CTCF	chr4:70089045-70089320	MCF-7	breast:	n/a	n/a
50	CTCF	chr4:70089071-70089282	HepG2	liver:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:70064835-70064885	IMR90	lung:	fetal
2	chr4:70080453-70080503	SAEC	small airway:	n/a
3	chr4:70080453-70080503	AG09309	skin:	n/a
4	chr4:70066318-70066368	AG09309	skin:	n/a
5	chr4:70155747-70155797	A549	lung:	n/a
6	chr4:70155747-70155797	Hepatocyte	liver:	n/a
7	chr4:70064835-70064885	NHDF-neo	bronchial:	n/a
8	chr4:70066318-70066368	HMEC	breast:	n/a
9	chr4:70080453-70080503	Jurkat	blood:	n/a
10	chr4:70155747-70155797	SAEC	small airway:	n/a
11	chr4:70080453-70080503	AG04450	lung:	fetal
12	chr4:70065325-70065375	U87	brain:	n/a
13	chr4:70064835-70064885	HRE	kidney:	n/a
14	chr4:70065325-70065375	PANC-1	pancreas:	n/a
15	chr4:70064835-70064885	ECC-1	luminal epithelium:	n/a
16	chr4:70155747-70155797	Hela-S3	cervix:	n/a
17	chr4:70066318-70066368	SK-N-MC	brain:	n/a
18	chr4:70066318-70066368	PrEC	prostate:	n/a
19	chr4:70080453-70080503	ECC-1	luminal epithelium:	n/a
20	chr4:70065325-70065375	T-47D	breast:	n/a
21	chr4:70080453-70080503	GM12891	blood:	n/a
22	chr4:70065325-70065375	HRCEpiC	kidney:	n/a
23	chr4:70155747-70155797	GM12891	blood:	n/a
24	chr4:70065325-70065375	SK-N-SH_RA	brain:	n/a
25	chr4:70065325-70065375	RPTEC	kidney:	n/a
26	chr4:70064835-70064885	HRCEpiC	kidney:	n/a
27	chr4:70066318-70066368	Caco-2	colon:	n/a
28	chr4:70066318-70066368	HRCEpiC	kidney:	n/a
29	chr4:70066318-70066368	HNPCEpiC	eye:	n/a
30	chr4:70066318-70066368	A549	lung:	n/a
31	chr4:70065325-70065375	HCM	heart:	n/a
32	chr4:70064835-70064885	CMK	blood:	n/a
33	chr4:70066318-70066368	GM06990	blood:	n/a
34	chr4:70080453-70080503	HEEpiC	esophagus:	n/a
35	chr4:70066318-70066368	Jurkat	blood:	n/a
36	chr4:70066318-70066368	K562	blood:	n/a
37	chr4:70080453-70080503	T-47D	breast:	n/a
38	chr4:70155747-70155797	LNCaP	prostate:	n/a
39	chr4:70066318-70066368	NHBE	bronchial:	n/a
40	chr4:70065325-70065375	HEK293	kidney:	embryo
41	chr4:70080453-70080503	H1-hESC	embryonic stem cell:	embryo
42	chr4:70155747-70155797	HNPCEpiC	eye:	n/a
43	chr4:70065325-70065375	AG04450	lung:	fetal
44	chr4:70155747-70155797	SK-N-SH	brain:	n/a
45	chr4:70064835-70064885	HCPEpiC	choroid plexus:	n/a
46	chr4:70065325-70065375	HPAEpiC	pulmonary alveolar:	n/a
47	chr4:70155747-70155797	GM12892	blood:	n/a
48	chr4:70065325-70065375	HNPCEpiC	eye:	n/a
49	chr4:70080453-70080503	HepG2	liver:	n/a
50	chr4:70080453-70080503	ovcar-3	ovarian:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr4:70060045..70062674-chr4:70067007..70069842,2	MCF-7	breast:
2	chr4:69673177..69674687-chr4:70085938..70087696,2	MCF-7	breast:
3	chr4:70060045..70062674-chr4:70067007..70069842,2	MCF-7	breast:
4	chr4:69789542..69791043-chr4:70152702..70154403,2	MCF-7	breast:
5	chr20:45932378..45933054-chr4:70163468..70164237,2	MCF-7	breast:

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

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

No data

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

Extended variants
information (count: 1953 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:1953 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10016939	chr4:70057009-70057010	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs77220320	chr4:70057017-70057018	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs375178638	chr4:70057021-70057022	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs35889317	chr4:70057024-70057025	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs76845118	chr4:70057029-70057030	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs542621419	chr4:70057066-70057067	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs143611725	chr4:70057110-70057111	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs528398567	chr4:70057175-70057176	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs368256910	chr4:70057210-70057211	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs540383738	chr4:70057235-70057236	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs185609047	chr4:70057243-70057244	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs573622301	chr4:70057302-70057303	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs116653498	chr4:70057388-70057389	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs116709140	chr4:70057403-70057404	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs370684109	chr4:70057424-70057425	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs148053666	chr4:70057426-70057427	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs375995518	chr4:70057429-70057430	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs538121140	chr4:70057431-70057432	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs72639750	chr4:70057432-70057433	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs533465396	chr4:70057433-70057434	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs546753748	chr4:70057434-70057435	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs566706488	chr4:70057439-70057440	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs7662857	chr4:70057441-70057442	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs140872267	chr4:70057464-70057465	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs144818450	chr4:70057470-70057471	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs538198438	chr4:70057472-70057473	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs530110060	chr4:70057474-70057475	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs6600906	chr4:70057573-70057574	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs62298911	chr4:70057610-70057611	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs539357636	chr4:70057616-70057617	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs534096289	chr4:70057631-70057632	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs6600907	chr4:70057718-70057719	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs569497904	chr4:70057765-70057766	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs573759902	chr4:70057791-70057792	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs189335538	chr4:70057819-70057820	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs6820542	chr4:70057839-70057840	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs576069466	chr4:70057860-70057861	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs138662497	chr4:70057862-70057863	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs555163302	chr4:70057877-70057878	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs564563472	chr4:70057913-70057914	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs114713111	chr4:70057920-70057921	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs6825376	chr4:70057930-70057931	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs560455408	chr4:70057940-70057941	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs180838819	chr4:70057941-70057942	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs549314829	chr4:70057951-70057952	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs142087020	chr4:70057957-70057958	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs185318993	chr4:70057959-70057960	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs188717485	chr4:70057988-70057989	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs112125335	chr4:70058038-70058039	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs566145840	chr4:70058044-70058045	Enhancers	n/a	n/a	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
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

Chromatin state (count:55 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:70056400-70057600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr4:70056400-70058400	Enhancers	HepG2	liver
3	chr4:70057400-70058000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr4:70057600-70057800	Enhancers	Liver	Liver
5	chr4:70058200-70058400	ZNF genes & repeats	Liver	Liver
6	chr4:70058400-70059000	Weak transcription	Liver	Liver
7	chr4:70059000-70059800	Enhancers	Liver	Liver
8	chr4:70059800-70060400	Enhancers	HepG2	liver
9	chr4:70059800-70066800	Weak transcription	Liver	Liver
10	chr4:70060000-70060400	Enhancers	Stomach Mucosa	stomach
11	chr4:70060000-70060800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr4:70062000-70063200	Enhancers	HMEC	breast
13	chr4:70062400-70063000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr4:70062600-70063400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr4:70066800-70067800	Strong transcription	Liver	Liver
16	chr4:70067800-70070600	Weak transcription	Liver	Liver
17	chr4:70076400-70076600	Enhancers	HUES48 Cell Line	embryonic stem cell
18	chr4:70076800-70077800	Weak transcription	HUES48 Cell Line	embryonic stem cell
19	chr4:70077800-70078200	Enhancers	HUES48 Cell Line	embryonic stem cell
20	chr4:70080400-70080800	Enhancers	HepG2	liver
21	chr4:70080600-70081200	Enhancers	Rectal Smooth Muscle	rectum
22	chr4:70080800-70081200	Enhancers	A549	lung
23	chr4:70085800-70086000	Enhancers	Fetal Intestine Large	intestine
24	chr4:70086000-70086400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr4:70086000-70087000	Weak transcription	Fetal Intestine Large	intestine
26	chr4:70086400-70087400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr4:70087000-70087600	Enhancers	Fetal Intestine Large	intestine
28	chr4:70087200-70088600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
29	chr4:70087400-70087600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr4:70088600-70090200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
31	chr4:70090200-70091000	Enhancers	ES-I3 Cell Line	embryonic stem cell
32	chr4:70090400-70090600	Enhancers	HepG2	liver
33	chr4:70090600-70091000	Enhancers	HUES48 Cell Line	embryonic stem cell
34	chr4:70090600-70091000	Enhancers	iPS-15b Cell Line	embryonic stem cell
35	chr4:70090600-70091000	Enhancers	Fetal Stomach	stomach
36	chr4:70104600-70106600	Enhancers	Fetal Intestine Large	intestine
37	chr4:70105000-70106600	Enhancers	Fetal Intestine Small	intestine
38	chr4:70105000-70106600	Enhancers	HepG2	liver
39	chr4:70105200-70106000	Enhancers	Rectal Mucosa Donor 29	rectum
40	chr4:70105200-70106400	Enhancers	Duodenum Mucosa	Duodenum
41	chr4:70105200-70106400	Enhancers	Rectal Mucosa Donor 31	rectum
42	chr4:70105200-70106600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr4:70105200-70106800	Enhancers	Stomach Mucosa	stomach
44	chr4:70105400-70105800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
45	chr4:70105400-70106200	Enhancers	Primary hematopoietic stem cells short term culture	blood
46	chr4:70106200-70106600	Enhancers	Small Intestine	intestine
47	chr4:70106600-70108400	Weak transcription	HepG2	liver
48	chr4:70108400-70108800	Enhancers	HepG2	liver
49	chr4:70111600-70112000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr4:70112000-70113400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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