Variant report

Variant	esv1822229
Chromosome Location	chr4:70027604-70301297
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1796)
CpG islands
(count:306)
Chromatin interactive
region (count:21)
LncRNA
region (count:12)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1796 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

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	chr4:70105540-70105900	HepG2	liver:	n/a	n/a
3	ARID3A	chr4:70254846-70255212	HepG2	liver:	n/a	n/a
4	ARID3A	chr4:70036297-70036563	HepG2	liver:	n/a	n/a
5	ARID3A	chr4:70047409-70047599	HepG2	liver:	n/a	n/a
6	ARID3A	chr4:70296492-70296919	K562	blood:	n/a	n/a
7	ARID3A	chr4:70056442-70056604	HepG2	liver:	n/a	n/a
8	ARID3A	chr4:70210667-70210694	HepG2	liver:	n/a	n/a
9	ARID3A	chr4:70296492-70296914	HepG2	liver:	n/a	n/a
10	ARID3A	chr4:70105523-70105754	K562	blood:	n/a	n/a
11	ARID3A	chr4:70106482-70106878	HepG2	liver:	n/a	n/a
12	ARID3A	chr4:70274315-70274516	HepG2	liver:	n/a	n/a
13	ARID3A	chr4:70045525-70045926	HepG2	liver:	n/a	n/a
14	ATF1	chr4:70105493-70105808	K562	blood:	n/a	n/a
15	ATF1	chr4:70296489-70296914	K562	blood:	n/a	n/a
16	ATF1	chr4:70187845-70188142	K562	blood:	n/a	n/a
17	ATF1	chr4:70087666-70087866	K562	blood:	n/a	n/a
18	ATF1	chr4:70044510-70044858	K562	blood:	n/a	n/a
19	ATF1	chr4:70175307-70175700	K562	blood:	n/a	n/a
20	ATF1	chr4:70033053-70033356	K562	blood:	n/a	n/a
21	ATF2	chr4:70033061-70033352	GM12878	blood:	n/a	n/a
22	ATF2	chr4:70032979-70033329	GM12878	blood:	n/a	n/a
23	ATF3	chr4:70296552-70296826	A549	lung:	n/a	n/a
24	ATF3	chr4:70296499-70296777	HepG2	liver:	n/a	n/a
25	ATF3	chr4:70296574-70296796	H1-hESC	embryonic stem cell:	n/a	n/a
26	ATF3	chr4:70296558-70296973	A549	lung:	n/a	n/a
27	BACH1	chr4:70097393-70097475	K562	blood:	n/a	n/a
28	BACH1	chr4:70036465-70036545	H1-hESC	embryonic stem cell:	n/a	n/a
29	BACH1	chr4:70296489-70296908	K562	blood:	n/a	n/a
30	BACH1	chr4:70033076-70033245	K562	blood:	n/a	n/a
31	BATF	chr4:70296590-70296824	GM12878	blood:	n/a	n/a
32	BATF	chr4:70033033-70033336	GM12878	blood:	n/a	chr4:70033221-70033232
33	BATF	chr4:70296589-70296863	GM12878	blood:	n/a	chr4:70296823-70296832
34	BCL11A	chr4:70296551-70296867	GM12878	blood:	n/a	n/a
35	BCL11A	chr4:70296603-70296770	H1-hESC	embryonic stem cell:	n/a	n/a
36	BCL11A	chr4:70296569-70296786	H1-hESC	embryonic stem cell:	n/a	n/a
37	BCL11A	chr4:70296596-70296779	GM12878	blood:	n/a	n/a
38	BCL3	chr4:70296436-70296843	A549	lung:	n/a	n/a
39	BCL3	chr4:70296548-70296829	A549	lung:	n/a	n/a
40	BCL3	chr4:70080358-70080837	A549	lung:	n/a	n/a
41	BCLAF1	chr4:70296549-70296826	GM12878	blood:	n/a	n/a
42	BHLHE40	chr4:70296485-70296909	GM12878	blood:	n/a	n/a
43	BHLHE40	chr4:70047447-70047661	HepG2	liver:	n/a	n/a
44	BHLHE40	chr4:70044628-70044869	K562	blood:	n/a	n/a
45	BHLHE40	chr4:70209675-70209715	K562	blood:	n/a	n/a
46	BHLHE40	chr4:70105574-70105707	K562	blood:	n/a	n/a
47	BHLHE40	chr4:70296483-70296924	K562	blood:	n/a	n/a
48	BHLHE40	chr4:70087582-70087589	K562	blood:	n/a	n/a
49	BHLHE40	chr4:70057696-70057810	K562	blood:	n/a	n/a
50	BRCA1	chr4:70296484-70296924	GM12878	blood:	n/a	n/a

(count:306 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:70080453-70080503	MCF-7	breast:	n/a
2	chr4:70080453-70080503	MCF-7	breast:	n/a
3	chr4:70064835-70064885	HIPEpiC	eye:	n/a
4	chr4:70064835-70064885	H1-hESC	embryonic stem cell:	embryo
5	chr4:70155747-70155797	NH-A	brain:	n/a
6	chr4:70064835-70064885	HEK293	kidney:	embryo
7	chr4:70066318-70066368	AG04449	skin:	fetal
8	chr4:70155747-70155797	AG09319	gingival:	n/a
9	chr4:70064835-70064885	GM19239	blood:	n/a
10	chr4:70065325-70065375	GM12892	blood:	n/a
11	chr4:70064835-70064885	A549	lung:	n/a
12	chr4:70066318-70066368	HIPEpiC	eye:	n/a
13	chr4:70064835-70064885	T-47D	breast:	n/a
14	chr4:70065325-70065375	PANC-1	pancreas:	n/a
15	chr4:70066318-70066368	NHDF-neo	bronchial:	n/a
16	chr4:70066318-70066368	SAEC	small airway:	n/a
17	chr4:70064835-70064885	HPAEpiC	pulmonary alveolar:	n/a
18	chr4:70155747-70155797	GM06990	blood:	n/a
19	chr4:70065325-70065375	HL-60	blood:	n/a
20	chr4:70065325-70065375	NT2-D1	testis:	n/a
21	chr4:70065325-70065375	HRE	kidney:	n/a
22	chr4:70155747-70155797	NB4	blood:	n/a
23	chr4:70066318-70066368	AG10803	skin:	n/a
24	chr4:70064835-70064885	HMEC	breast:	n/a
25	chr4:70080453-70080503	GM12892	blood:	n/a
26	chr4:70064835-70064885	SKMC	muscle:	n/a
27	chr4:70064835-70064885	RPTEC	kidney:	n/a
28	chr4:70064835-70064885	HRCEpiC	kidney:	n/a
29	chr4:70155747-70155797	A549	lung:	n/a
30	chr4:70066318-70066368	AG09309	skin:	n/a
31	chr4:70080453-70080503	SK-N-MC	brain:	n/a
32	chr4:70066318-70066368	HL-60	blood:	n/a
33	chr4:70064835-70064885	HL-60	blood:	n/a
34	chr4:70066318-70066368	NHBE	bronchial:	n/a
35	chr4:70066318-70066368	GM12878	blood:	n/a
36	chr4:70066318-70066368	H1-hESC	embryonic stem cell:	embryo
37	chr4:70155747-70155797	HepG2	liver:	n/a
38	chr4:70155747-70155797	PrEC	prostate:	n/a
39	chr4:70066318-70066368	GM06990	blood:	n/a
40	chr4:70080453-70080503	AG10803	skin:	n/a
41	chr4:70064835-70064885	BJ	skin:	n/a
42	chr4:70066318-70066368	LNCaP	prostate:	n/a
43	chr4:70066318-70066368	NB4	blood:	n/a
44	chr4:70155747-70155797	HCPEpiC	choroid plexus:	n/a
45	chr4:70064835-70064885	NHBE	bronchial:	n/a
46	chr4:70080453-70080503	HEK293	kidney:	embryo
47	chr4:70064835-70064885	GM06990	blood:	n/a
48	chr4:70065325-70065375	T-47D	breast:	n/a
49	chr4:70065325-70065375	SKMC	muscle:	n/a
50	chr4:70065325-70065375	HAEpiC	amniotic membrane:	n/a

(count:21 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:70024955..70027798-chr4:70029828..70032326,2	K562	blood:
2	chr4:70188461..70190645-chr4:70191525..70193153,2	K562	blood:
3	chr19:24183615..24184637-chr4:70296138..70296644,3	K562	blood:
4	chr19:36066562..36067220-chr4:70296617..70297159,2	MCF-7	breast:
5	chr4:70262708..70264895-chr4:70280098..70283006,2	K562	blood:
6	chr4:70024955..70027798-chr4:70029828..70032326,2	K562	blood:
7	chr4:70183340..70184245-chr4:70482427..70483057,3	MCF-7	breast:
8	chr21:9824058..9826515-chr4:70295211..70298169,2	K562	blood:
9	chr19:24184130..24184632-chr4:70296678..70297183,2	MCF-7	breast:
10	chr2:133011384..133014243-chr4:70295163..70298145,2	K562	blood:
11	chr4:70183605..70184238-chr4:70482598..70483352,3	MCF-7	breast:
12	chr2:133038471..133039156-chr4:70296229..70297178,3	MCF-7	breast:
13	chr4:69789542..69791043-chr4:70152702..70154403,2	MCF-7	breast:
14	chr21:9825015..9827465-chr4:70296669..70298179,2	K562	blood:
15	chr4:70262708..70264895-chr4:70280098..70283006,2	K562	blood:
16	chr4:69673177..69674687-chr4:70085938..70087696,2	MCF-7	breast:
17	chr4:70296625..70297182-chr6:133594074..133594625,3	MCF-7	breast:
18	chr20:45932378..45933054-chr4:70163468..70164237,2	MCF-7	breast:
19	chr4:70188461..70190645-chr4:70191525..70193153,2	K562	blood:
20	chr4:70060045..70062674-chr4:70067007..70069842,2	MCF-7	breast:
21	chr4:70060045..70062674-chr4:70067007..70069842,2	MCF-7	breast:

(count:12 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-UGT2B28-1	chr4:70066138-70066296	ENSG00000250696.1
2	lnc-UGT2B28-1	chr4:70080191-70080193	ENSG00000250696.1
3	lnc-UGT2B28-1	chr4:70066190-70066296	ENSG00000250696.1
4	lnc-UGT2B28-1	chr4:70047378-70048090	NONHSAT096756
5	lnc-UGT2B28-1	chr4:70047818-70048090	ENSG00000250696.1
6	lnc-UGT2B28-1	chr4:70061386-70061489	ENSG00000250696.1
7	lnc-UGT2B28-1	chr4:70076784-70076865	ENSG00000250696.1
8	lnc-UGT2B28-1	chr4:70076784-70076865	ENSG00000250696.1
9	lnc-UGT2B28-1	chr4:70080191-70082484	ENSG00000250696.1
10	lnc-UGT2B28-5	chr4:70272649-70273373	NONHSAT096764
11	lnc-UGT2B28-4	chr4:70253298-70254025	NONHSAT096763
12	lnc-UGT2B28-1	chr4:70066890-70067002	ENSG00000250696.1

No data

Variant related genes	Relation type
ENSG00000251691	TF binding region
ENSG00000248824	TF binding region
ENSG00000196472	TF binding region
ENSG00000250696	TF binding region
ENSG00000268209	TF binding region
ENSG00000268803	TF binding region
ENSG00000215110	TF binding region
ENSG00000250828	TF binding region
ENSG00000249956	TF binding region
UGT2B11	TF binding region
ENSG00000249763	TF binding region
ENSG00000250612	TF binding region
UGT2B28	TF binding region
ENSG00000251691	CpG island
ENSG00000248824	CpG island
ENSG00000196472	CpG island
ENSG00000250696	CpG island
ENSG00000268209	CpG island
ENSG00000268803	CpG island
ENSG00000215110	CpG island
ENSG00000250828	CpG island
ENSG00000249956	CpG island
UGT2B11	CpG island
ENSG00000249763	CpG island
ENSG00000250612	CpG island
UGT2B28	CpG island
ENSG00000264462	chromatin interactions
ENSG00000198277	chromatin interactions
ENSG00000264063	chromatin interactions

Extended variants
information (count: 4883 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:4883 , 50 per page) page: 1 2 3 4 5 6 7 ... 98

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs576540399	chr4:70027640-70027641	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs189577572	chr4:70027644-70027645	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs181458846	chr4:70027645-70027646	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs574392746	chr4:70027648-70027649	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs539829519	chr4:70027664-70027665	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs184682279	chr4:70027665-70027666	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs189452452	chr4:70027671-70027672	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs142933538	chr4:70027692-70027693	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs560046205	chr4:70027693-70027694	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs536577907	chr4:70027715-70027716	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs182007634	chr4:70027716-70027717	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs185886596	chr4:70027747-70027748	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs553949232	chr4:70027752-70027753	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs532297724	chr4:70027761-70027762	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs558687584	chr4:70027777-70027778	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs572040892	chr4:70027780-70027781	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs540685231	chr4:70027783-70027784	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs552010794	chr4:70027794-70027795	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs147419285	chr4:70027884-70027885	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs574227357	chr4:70027888-70027889	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs543348771	chr4:70027905-70027906	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs562903140	chr4:70027951-70027952	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs190894329	chr4:70027966-70027967	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs180874326	chr4:70027974-70027975	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs139675955	chr4:70028019-70028020	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs373889297	chr4:70028073-70028074	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs527815720	chr4:70028088-70028089	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs531527481	chr4:70028110-70028111	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs547455030	chr4:70028123-70028124	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs567700396	chr4:70028129-70028130	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs536145402	chr4:70028131-70028132	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs186346009	chr4:70028161-70028162	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs190267009	chr4:70028180-70028181	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs377548710	chr4:70028228-70028229	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs115184069	chr4:70028231-70028232	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs558648712	chr4:70028246-70028247	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs572153208	chr4:70028247-70028248	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs534741709	chr4:70028252-70028253	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs554263118	chr4:70028255-70028256	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs574385013	chr4:70028263-70028264	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs182878499	chr4:70028272-70028273	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs562866629	chr4:70028273-70028274	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs568525854	chr4:70028284-70028285	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs187480691	chr4:70028290-70028291	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs545181363	chr4:70028296-70028297	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs190837626	chr4:70028345-70028346	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs556122021	chr4:70028347-70028348	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs367883835	chr4:70028348-70028349	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs527782568	chr4:70028355-70028356	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs547910789	chr4:70028363-70028364	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:92)

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
Chronic lymphocytic leukemia	21215367	CNVD

Chromatin state (count:323 , 50 per page) page: 1 2 3 4 5 6 7

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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